ID stringlengths 13 17 | question stringlengths 88 1.13k | answer stringlengths 6 156 | reference_sequence stringlengths 4.1k 4.1k | variant_sequence stringlengths 4.1k 4.1k |
|---|---|---|---|---|
Task1_train_42400 | Given a variant located on Chromosome 12, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | ACGCTGGTAACCACCAACTTTCTAATTCAGATAGCCCCAGCCCACACTGTTTTGGGAATGCTGAAAGTTGTTGCCTGTTAGGTTTAGGAATTCACATAGATATATATCCCTTTTTAGAATGCTTTCAGGTATCTATAAGGATATCTTGCTGTCAAAAAACTTAGGATTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGGCCGGACTGCGGACTGCAGTGGCGCAATCTCGGCTCACTGCAAGCTCCGCTTCCCGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGC... | ACGCTGGTAACCACCAACTTTCTAATTCAGATAGCCCCAGCCCACACTGTTTTGGGAATGCTGAAAGTTGTTGCCTGTTAGGTTTAGGAATTCACATAGATATATATCCCTTTTTAGAATGCTTTCAGGTATCTATAAGGATATCTTGCTGTCAAAAAACTTAGGATTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGGCCGGACTGCGGACTGCAGTGGCGCAATCTCGGCTCACTGCAAGCTCCGCTTCCCGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGC... |
Task1_train_42401 | A mutation found on Chromosome 12 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GACAGGGTTTCTCCATGTTGGTCAGGCTGGTCTCAAACTCCCGACCTCAGGTGATCCACCCGCCTCAGCCTCCCAACAGTGCTGGGATTACAGGTGTGAGCCACTGTGCCCGGCTGAATATTTCTAATGTCTAGGGATTTGTGGTTTAGGGACTGACAGGGACAAAATTCCAGCTCTCAAAAGGCTTACAGACACAAATTTTTCTAAAAAATAGTTATAAAGGATATAAAAGCAAAGAAGCAGGTAGAAGGGTGAAGAATGAAAGGAGACATTGTTTTAGAAGACACCTCACATAGGGAATATTTGAGTAGAGACCTAAC... | GACAGGGTTTCTCCATGTTGGTCAGGCTGGTCTCAAACTCCCGACCTCAGGTGATCCACCCGCCTCAGCCTCCCAACAGTGCTGGGATTACAGGTGTGAGCCACTGTGCCCGGCTGAATATTTCTAATGTCTAGGGATTTGTGGTTTAGGGACTGACAGGGACAAAATTCCAGCTCTCAAAAGGCTTACAGACACAAATTTTTCTAAAAAATAGTTATAAAGGATATAAAAGCAAAGAAGCAGGTAGAAGGGTGAAGAATGAAAGGAGACATTGTTTTAGAAGACACCTCACATAGGGAATATTTGAGTAGAGACCTAAC... |
Task1_train_42402 | This variant is located on Chromosome 12. Evaluate its biological effect and specify any disease association. | Benign | TCCTGGGCTCAAGGGCTCCTCCCACCCCAGCCTCCAGAGCAGCTGGGACTACAGGCACACACCACCACACTGGCTAATTTTTTAACTTTTTGTAGAGATGGACTCTTACTATGTTGCCCAGGCTGGTCTCAAACTCCTGTGCTCAAGCTGCTCTCTCACCTCAGCCTCCCAAAGTGCTGGGATTATAGGTGTGAGCCACCACACCCAGCCTGATCAGTGAATATTTAGCACTTACCATGTGCTTGAGATATATCAGTGAACAAGCAAGCAAACAATAAATGGAACAAACACGTCAATAGTATTGAGTGCTAGAAGATGAT... | TCCTGGGCTCAAGGGCTCCTCCCACCCCAGCCTCCAGAGCAGCTGGGACTACAGGCACACACCACCACACTGGCTAATTTTTTAACTTTTTGTAGAGATGGACTCTTACTATGTTGCCCAGGCTGGTCTCAAACTCCTGTGCTCAAGCTGCTCTCTCACCTCAGCCTCCCAAAGTGCTGGGATTATAGGTGTGAGCCACCACACCCAGCCTGATCAGTGAATATTTAGCACTTACCATGTGCTTGAGATATATCAGTGAACAAGCAAGCAAACAATAAATGGAACAAACACGTCAATAGTATTGAGTGCTAGAAGATGAT... |
Task1_train_42403 | A variant was discovered on Chromosome 12. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TAACTGTACATTTAAGGATCATGTGTGTATTAGAAAATTTTACACAATTTATGTGCTACAAAGTTTCATTAGAGACTTTACAGTTTTTCTGATGATCTAGTACTTCTCTATGGACTTCTTTTTCTGTTGATGCTTCCCTACCCCCTCCCTACCTTAAGGTATTTTTCTAGAATTAGTTTGCAATAATCATTACCAGCTTCCCTACTTGAGCGTACGTCTTCTGAAAACCACCCTGCTTTTCCCTTTGTGGTAGAATGGCAGCTCAGTTACAGAAACATGCTATAATTAAGGTATATATAGCTTCCTTTTATGATACAGGC... | TAACTGTACATTTAAGGATCATGTGTGTATTAGAAAATTTTACACAATTTATGTGCTACAAAGTTTCATTAGAGACTTTACAGTTTTTCTGATGATCTAGTACTTCTCTATGGACTTCTTTTTCTGTTGATGCTTCCCTACCCCCTCCCTACCTTAAGGTATTTTTCTAGAATTAGTTTGCAATAATCATTACCAGCTTCCCTACTTGAGCGTACGTCTTCTGAAAACCACCCTGCTTTTCCCTTTGTGGTAGAATGGCAGCTCAGTTACAGAAACATGCTATAATTAAGGTATATATAGCTTCCTTTTATGATACAGGC... |
Task1_train_42404 | An alteration has been detected on Chromosome 12. Is it pathogenic, and if so, what disease is involved? | Benign | CCACCCAATCAAACTGAGGTGAGTTTAGACCCTTCAATATGGCCCTTCTAAAGGCTGTGGCTTCATTCTATCTCCTCCCAAGGTACAGGTAGCTGCTGTAACAACCCTTGCACATTCCCAATTATAATGAAATGGGTGAATCAAAGGTCAACTTCCCAGGGTCAAATCCCAGGCATTCCTTCTTTTGCAAGGCCTGCCTGATGTCTATTCCTGCACAAGCTATAGACTAAACTGCATTACTGTGGAAGGTTCTTGTCACTTTGTCTCCACTAGGTATTCTTGCTGCTCAATAGAACCCTTTTTAAAAGAGAAGCACTCTG... | CCACCCAATCAAACTGAGGTGAGTTTAGACCCTTCAATATGGCCCTTCTAAAGGCTGTGGCTTCATTCTATCTCCTCCCAAGGTACAGGTAGCTGCTGTAACAACCCTTGCACATTCCCAATTATAATGAAATGGGTGAATCAAAGGTCAACTTCCCAGGGTCAAATCCCAGGCATTCCTTCTTTTGCAAGGCCTGCCTGATGTCTATTCCTGCACAAGCTATAGACTAAACTGCATTACTGTGGAAGGTTCTTGTCACTTTGTCTCCACTAGGTATTCTTGCTGCTCAATAGAACCCTTTTTAAAAGAGAAGCACTCTG... |
Task1_train_42405 | This mutation on Chromosome 12 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | AAATGTCTAATTGTTTTGTTTTATAGATTGGCATAAACCCGGGACTAATGGCTGCTTACAAAGGGCATCATTACCCTGGACCTGGAAACCATTTTTGTAAGTGGTTACCTTTTAAATTAATTTACTTTTAAATTAGGTATCTTTGTTAACAGGTTTTTTCAGAAAAACCAATTGTGTTTTTAAAAAGAAAGAGACTGTAAATACACATTCGTGTTTCATGTTCTGTGTGTGTGTCTGTACGTGAAAATAAGAGAGTTTGAAATGATATGTTACTGTTAACATTTTAGTCTATGAGAATGGAGGGATGTGAATAAGAGTAC... | AAATGTCTAATTGTTTTGTTTTATAGATTGGCATAAACCCGGGACTAATGGCTGCTTACAAAGGGCATCATTACCCTGGACCTGGAAACCATTTTTGTAAGTGGTTACCTTTTAAATTAATTTACTTTTAAATTAGGTATCTTTGTTAACAGGTTTTTTCAGAAAAACCAATTGTGTTTTTAAAAAGAAAGAGACTGTAAATACACATTCGTGTTTCATGTTCTGTGTGTGTGTCTGTACGTGAAAATAAGAGAGTTTGAAATGATATGTTACTGTTAACATTTTAGTCTATGAGAATGGAGGGATGTGAATAAGAGTAC... |
Task1_train_42406 | Chromosome 12 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CAGCTTGCCCAAGGTATGTTACTGTCCTCATTCCTTTTATTCATTTTGTGTGTGTATATATACACATATATACTTACATATATATACACATATACATATATACATATACACATATACATATGTGTGCACATATATGCACACGTGTATATATACATGTGTATATATACATATATACACATAAGTATGTATGTCTATATACATATATGTGTGTATACACTTGTGTGCGTATACATATGTGTGTGTCTATATATAGACACATACACACACACACACACACACACACACACACACACACACACACATTACAGAAAGTATCTTAT... | CAGCTTGCCCAAGGTATGTTACTGTCCTCATTCCTTTTATTCATTTTGTGTGTGTATATATACACATATATACTTACATATATATACACATATACATATATACATATACACATATACATATGTGTGCACATATATGCACACGTGTATATATACATGTGTATATATACATATATACACATAAGTATGTATGTCTATATACATATATGTGTGTATACACTTGTGTGCGTATACATATGTGTGTGTCTATATATAGACACATACACACACACACACACACACACACACACACACACACACACACATTACAGAAAGTATCTTAT... |
Task1_train_42407 | A variant on Chromosome 12 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TCACACCTTGATCCTGGACTTCCAGCCTCCAGAACCAGAGAAAATACATTTCTATGGTCTAGCCACCTAGTCTGTGCTATTTTGTTATGGCAGCCCAAGCAAACGAATACAGATTTTTAAAAATTTACCCATTGTAAGCGTACAGTACAATGATGTTTAGTAAATTTATAGAATTGCACAACCATCACCAAGATCCAATTTTAGAAAGTTCCATTGAGCTGCCTGGTCTGCAGTCAGTCCATTCCCACTCCCAGCTCTAGGCAACCACTGATCTGCTCTGTGTCTCCATAGATTTTCCTTTTCTAGAAATTTCATATAGA... | TCACACCTTGATCCTGGACTTCCAGCCTCCAGAACCAGAGAAAATACATTTCTATGGTCTAGCCACCTAGTCTGTGCTATTTTGTTATGGCAGCCCAAGCAAACGAATACAGATTTTTAAAAATTTACCCATTGTAAGCGTACAGTACAATGATGTTTAGTAAATTTATAGAATTGCACAACCATCACCAAGATCCAATTTTAGAAAGTTCCATTGAGCTGCCTGGTCTGCAGTCAGTCCATTCCCACTCCCAGCTCTAGGCAACCACTGATCTGCTCTGTGTCTCCATAGATTTTCCTTTTCTAGAAATTTCATATAGA... |
Task1_train_42408 | A mutation has occurred on Chromosome 12. What is the medical relevance of this mutation? | Benign | TTTTGAGATGGAGTCTCACTCTGTAGCCCAGGCTGGAGTGCAGTGGCATGATCTTGGCTCACTGTGAGCTCCGCCTCCCGGGTTCACGCCATTCTCCTGCCTCAGCCTCTCGAGTAGCTGGGACTACAGGCGCCTGCCACCACGCCCAGCTAATTTTTTATATTTGTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCAGACCTCATGATCCACCCGCCTTGGCCTCTCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGCCTCGCTGCCCTTTTCACTCTTAATTCTCTTGCATGTAAACT... | TTTTGAGATGGAGTCTCACTCTGTAGCCCAGGCTGGAGTGCAGTGGCATGATCTTGGCTCACTGTGAGCTCCGCCTCCCGGGTTCACGCCATTCTCCTGCCTCAGCCTCTCGAGTAGCTGGGACTACAGGCGCCTGCCACCACGCCCAGCTAATTTTTTATATTTGTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCAGACCTCATGATCCACCCGCCTTGGCCTCTCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGCCTCGCTGCCCTTTTCACTCTTAATTCTCTTGCATGTAAACT... |
Task1_train_42409 | Here is a genetic alteration on Chromosome 12. Based on the data, is it a benign variant or a cause of disease? | Benign | TCTGTTGTTTCCTTCTTTGTGTTAATGAGCTTTCCTCATTTAGCTCCCACTTATAAATGAGAACATGTGGTATTTGGTTTTCTGTTCCTGTGCTAAGTTTGCCAAGGATAACAGCCCCAGCTCCATCCATGTTCCTGCAAAAGCTATGATCTCGTTCTTTTTCTTGGCTGCATAGTATTCCATGGTATATATGTACCACATTTTAAAAATCCAATCTGTCATTCAGGAGCATTTAGGTTGACTCCATGTTTTTGCTATTGTGAATAGTGCTGCAATGGGAAGATACATTCCCATGCATGTATCTTCATGGTATAATGATT... | TCTGTTGTTTCCTTCTTTGTGTTAATGAGCTTTCCTCATTTAGCTCCCACTTATAAATGAGAACATGTGGTATTTGGTTTTCTGTTCCTGTGCTAAGTTTGCCAAGGATAACAGCCCCAGCTCCATCCATGTTCCTGCAAAAGCTATGATCTCGTTCTTTTTCTTGGCTGCATAGTATTCCATGGTATATATGTACCACATTTTAAAAATCCAATCTGTCATTCAGGAGCATTTAGGTTGACTCCATGTTTTTGCTATTGTGAATAGTGCTGCAATGGGAAGATACATTCCCATGCATGTATCTTCATGGTATAATGATT... |
Task1_train_42410 | A mutation has occurred on Chromosome 12. What is the medical relevance of this mutation? | Benign | ATCTCTGTAAATCTCAGACTTTCTGAAAACTTCCTTAAGGAGAAATTTCTAGGACAAGGAAATGTGAACATTTAAAATTGTGGTACATATTGCCTAGCACTCCAAAAACACTTCACTATTGATATTCCCACTGATAATTTATACGAATGCTGCTGTTAGCAGGGTGCAGTGGCTCATGCCTGTAATCCAGCACTTTGAGAGGCTAAGATAGGTAGATCACTTGAGGCAAAGCATTTGAGACCAGCGTGGGCAACATGGCGAAACCTCATCTCTACTAATAATACCAAAATTAGCCGGGCATGGTGGCACATGCCTGAAGT... | ATCTCTGTAAATCTCAGACTTTCTGAAAACTTCCTTAAGGAGAAATTTCTAGGACAAGGAAATGTGAACATTTAAAATTGTGGTACATATTGCCTAGCACTCCAAAAACACTTCACTATTGATATTCCCACTGATAATTTATACGAATGCTGCTGTTAGCAGGGTGCAGTGGCTCATGCCTGTAATCCAGCACTTTGAGAGGCTAAGATAGGTAGATCACTTGAGGCAAAGCATTTGAGACCAGCGTGGGCAACATGGCGAAACCTCATCTCTACTAATAATACCAAAATTAGCCGGGCATGGTGGCACATGCCTGAAGT... |
Task1_train_42411 | A variant on Chromosome 12 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | CTTTGTGAACAACAGTATTCACTCACCACTGGATTTTTGAAGATACCAGTTCTTGTCTCTAAGGGAGCACTTTCTAGGCTATCTATCTTATGTAAAAAGTAGTGGGGGCAAAAGCAAGAGTAGTCTCTTCATTCCAGTACTAACATTTCAGATGGGTGCATTAGCCTTAAAAGGGGAATTAGCTGAAGCCATAAGAAAGTCTGAAAATAAAACTGAACGTACCTCAAAGATTGACTGGTGACCATCAGATGGGATTCTGTCATGCGGAAGATGTTATGAATAGCCCGAGCAGCCAATACTTGTCTCATCGCTTCATAAAT... | CTTTGTGAACAACAGTATTCACTCACCACTGGATTTTTGAAGATACCAGTTCTTGTCTCTAAGGGAGCACTTTCTAGGCTATCTATCTTATGTAAAAAGTAGTGGGGGCAAAAGCAAGAGTAGTCTCTTCATTCCAGTACTAACATTTCAGATGGGTGCATTAGCCTTAAAAGGGGAATTAGCTGAAGCCATAAGAAAGTCTGAAAATAAAACTGAACGTACCTCAAAGATTGACTGGTGACCATCAGATGGGATTCTGTCATGCGGAAGATGTTATGAATAGCCCGAGCAGCCAATACTTGTCTCATCGCTTCATAAAT... |
Task1_train_42412 | Here is a mutation located on Chromosome 12. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AGGCCATCTCGGTTTCAGAATTAAAAGAAAAAACAGCCTTAAAATAGTAAACTTACCTATTTGCTAATCGTTTATACCATGTGCTAATAAAACACATCATAATTACGAAATTCTCAGAATGTAACCACTCTGGAAAAGTCATAACAAAGCTCAAGTGTTTATTAAGAATTAAAAATACTGTAAATAAGCCATACAGTTCATTTCACAGTAAACTAAACAAAACTTTTTTTTTTTTTTTTTACTTTTCGGGTTTTTTTTTTTTTTTTTTTTTCAATTTTTTTTGGAAGGGCAAGACAGCCATTAAAGAACAATACAGCTCA... | AGGCCATCTCGGTTTCAGAATTAAAAGAAAAAACAGCCTTAAAATAGTAAACTTACCTATTTGCTAATCGTTTATACCATGTGCTAATAAAACACATCATAATTACGAAATTCTCAGAATGTAACCACTCTGGAAAAGTCATAACAAAGCTCAAGTGTTTATTAAGAATTAAAAATACTGTAAATAAGCCATACAGTTCATTTCACAGTAAACTAAACAAAACTTTTTTTTTTTTTTTTTACTTTTCGGGTTTTTTTTTTTTTTTTTTTTTCAATTTTTTTTGGAAGGGCAAGACAGCCATTAAAGAACAATACAGCTCA... |
Task1_train_42413 | A variant has been detected on Chromosome 12. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | AGGGTGAACATTCCATTTAGGATTTGGGGTTTGGTGGCAGTGAAAGGTTTGAAGTAGCCCCTTTTCTTCTGTCTTCTCTCGCCTTCCCCTGAGCAGATTGGAGTTTAAGCTCAGGTAGAATTTAGTCTTCATGAGTTAGAGGAGGCTGTTTCACCACTGAGGATGCAAGGGCTCAAGAATCTTATAGCCAGTGTTCATGGCTTTGGGATTCTGGGATAAGGTGAGTGTCTCCACTCCACTCCTTGCCCTTCAGCCTGCACAAGTGGACTCTAGTGGTTTTCTGCTTGCAAAAGTGGTGGGCTCAGCAAGGATACATTTCT... | AGGGTGAACATTCCATTTAGGATTTGGGGTTTGGTGGCAGTGAAAGGTTTGAAGTAGCCCCTTTTCTTCTGTCTTCTCTCGCCTTCCCCTGAGCAGATTGGAGTTTAAGCTCAGGTAGAATTTAGTCTTCATGAGTTAGAGGAGGCTGTTTCACCACTGAGGATGCAAGGGCTCAAGAATCTTATAGCCAGTGTTCATGGCTTTGGGATTCTGGGATAAGGTGAGTGTCTCCACTCCACTCCTTGCCCTTCAGCCTGCACAAGTGGACTCTAGTGGTTTTCTGCTTGCAAAAGTGGTGGGCTCAGCAAGGATACATTTCT... |
Task1_train_42414 | A change on Chromosome 12 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | AGCAAATTTACTCCTTTTAAGAAGGCCGAGCTATTTGGAAAGATGCCCACCAGGATGGCAAAGTGGTGCTTGAGCCCTCCCTGCAGCACACGCCCAGGACTTTGAAGCAGGGACAGGGTCCTCCTGGCTACTGAAAGGAATCGAGTTAACGCGCCCTAGTGGCAGGTGGCGAATGGCCGGAGATCCGGCCTCCCAGTGGTGTCCACCGCCACGGGCCTCCGCTCGACAGGCTTATTTCCCTCCATGCTGGAGCAAACCCCGGCTGAAAGAGGGCCGCACTAATTGGTTTGCGTACCCGAAGTGGGAATAGAGAGGGAGGA... | AGCAAATTTACTCCTTTTAAGAAGGCCGAGCTATTTGGAAAGATGCCCACCAGGATGGCAAAGTGGTGCTTGAGCCCTCCCTGCAGCACACGCCCAGGACTTTGAAGCAGGGACAGGGTCCTCCTGGCTACTGAAAGGAATCGAGTTAACGCGCCCTAGTGGCAGGTGGCGAATGGCCGGAGATCCGGCCTCCCAGTGGTGTCCACCGCCACGGGCCTCCGCTCGACAGGCTTATTTCCCTCCATGCTGGAGCAAACCCCGGCTGAAAGAGGGCCGCACTAATTGGTTTGCGTACCCGAAGTGGGAATAGAGAGGGAGGA... |
Task1_train_42415 | A mutation is present on Chromosome 12. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CGGCCTCCCAGTGGTGTCCACCGCCACGGGCCTCCGCTCGACAGGCTTATTTCCCTCCATGCTGGAGCAAACCCCGGCTGAAAGAGGGCCGCACTAATTGGTTTGCGTACCCGAAGTGGGAATAGAGAGGGAGGAAAACCATGTTTCAGGTGTTACGGGGGGAAAAAAGTGAAATGCGAACCGCAGGGGAGAGAGCGACCGTCAGGCAGACACCTTGTGAACCGCGGTGGAGAGCACACCTAGGTGGGGAGGTCACCGGCCCAACCCACCACCCTCCGGGAGAATGCGGGCAGGGACAGCAGCAGGGGGCAGCATCCACG... | CGGCCTCCCAGTGGTGTCCACCGCCACGGGCCTCCGCTCGACAGGCTTATTTCCCTCCATGCTGGAGCAAACCCCGGCTGAAAGAGGGCCGCACTAATTGGTTTGCGTACCCGAAGTGGGAATAGAGAGGGAGGAAAACCATGTTTCAGGTGTTACGGGGGGAAAAAAGTGAAATGCGAACCGCAGGGGAGAGAGCGACCGTCAGGCAGACACCTTGTGAACCGCGGTGGAGAGCACACCTAGGTGGGGAGGTCACCGGCCCAACCCACCACCCTCCGGGAGAATGCGGGCAGGGACAGCAGCAGGGGGCAGCATCCACG... |
Task1_train_42416 | Here’s a variant located on Chromosome 12. What is the predicted biological effect — harmless or disease-causing? | Benign | TTTATAGCAACATCTAGACTAGTGTTTGATCAAACAACTGGGCACCATAGCCTGGCCAAGTTGACACATAAAATTAACCATCACTGGCCAGGCGCGGTGGGTCACACCTGTAATCCCAGTACTTTGGGAGGCCAAGGCGGGCGGATCACCTGCGGTCTGGAGTTCGAGGCCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAAAATTAGCTGGGAGTGGTGGTGCATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCCGGGAGGCAGGGGTTGCAGTGAGCCGA... | TTTATAGCAACATCTAGACTAGTGTTTGATCAAACAACTGGGCACCATAGCCTGGCCAAGTTGACACATAAAATTAACCATCACTGGCCAGGCGCGGTGGGTCACACCTGTAATCCCAGTACTTTGGGAGGCCAAGGCGGGCGGATCACCTGCGGTCTGGAGTTCGAGGCCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAAAATTAGCTGGGAGTGGTGGTGCATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCCGGGAGGCAGGGGTTGCAGTGAGCCGA... |
Task1_train_42417 | A sequence alteration has been identified on Chromosome 12. Is it disease-inducing or harmless? | Benign | TAACTCCAGGAAATACAGGCGTTTAGATGCTAAGAGCCACGTTCCAAATGTCAACCAGGACCTCCGCAACGTTACCTCTGTATTACATCTAACCGTTTGAGACAGCTGTGGGATTTTATACAGAGGAGAAACCCATTCCACAAATGCATGGCTTAGCCAGCTCTTTTTTCCTAGTAAACCTGTCCCAAACTATTCAGTCATGAAAAGAGGCCCTGGAGCTTCCTGTGGCCCTTTCAGGGTGTCTCTTGAGAAAAAGAACAAGCTGGTTCATCAGATTGAATCTCAGCTGTTGTGGTTAAGTTCAACAGTGCATCATGATG... | TAACTCCAGGAAATACAGGCGTTTAGATGCTAAGAGCCACGTTCCAAATGTCAACCAGGACCTCCGCAACGTTACCTCTGTATTACATCTAACCGTTTGAGACAGCTGTGGGATTTTATACAGAGGAGAAACCCATTCCACAAATGCATGGCTTAGCCAGCTCTTTTTTCCTAGTAAACCTGTCCCAAACTATTCAGTCATGAAAAGAGGCCCTGGAGCTTCCTGTGGCCCTTTCAGGGTGTCTCTTGAGAAAAAGAACAAGCTGGTTCATCAGATTGAATCTCAGCTGTTGTGGTTAAGTTCAACAGTGCATCATGATG... |
Task1_train_42418 | Here’s a variant located on Chromosome 12. What is the predicted biological effect — harmless or disease-causing? | Benign | GAAAAGAGTTTTACAAAGAGATGGAAATAAAAATTACCTATATTCCTACTTGATTGGTCAGAGTTCTCTAGGGAAACAGAACCAACAGGATTAAAACCAATAGGATATGTGGATAGATATATTAAGAGATTTATTTTAAGGAAATTGGCTTACGCAATTGCGGGAGCTGGCAAGTCCGAAATTCATATGGCAGGCCAGCAGACTGGAAACTCAGGCAGCAGTTAATGCTGCGATCTTGAGATGGAATTCCTTCTTCTCCAGGAAGCCTTAGGTTTGCTTTTAAGTCCCTCAACTGATTGCATGAGGCTCACCCACATTAT... | GAAAAGAGTTTTACAAAGAGATGGAAATAAAAATTACCTATATTCCTACTTGATTGGTCAGAGTTCTCTAGGGAAACAGAACCAACAGGATTAAAACCAATAGGATATGTGGATAGATATATTAAGAGATTTATTTTAAGGAAATTGGCTTACGCAATTGCGGGAGCTGGCAAGTCCGAAATTCATATGGCAGGCCAGCAGACTGGAAACTCAGGCAGCAGTTAATGCTGCGATCTTGAGATGGAATTCCTTCTTCTCCAGGAAGCCTTAGGTTTGCTTTTAAGTCCCTCAACTGATTGCATGAGGCTCACCCACATTAT... |
Task1_train_42419 | A mutation on Chromosome 12 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | AGAAAAAAAAAAAAAAAAAAAAAAGTAGAAATGCTAACCACCTGCCAACCCCAACAGGTTCCTCTGACAATCAGATGTAATGGGTGGGACAAGCTATACCAATGGATGACATCACTATCTCATAACAAAAATATCAGTGCCAGAGAGAGTATTATAAGGAAACTGACACTCAGTAAGGTTTAATGAGTAAACTAGATTAGCAACTTCACATTCACTGAGTGATTTCACATCCAGTGTGGCATCTAGTCCACATTTTAAGTGTAAATCCCACTATGAATAACTTAAAGGAAATCATTTCATCATTTGTTCTGAACCTCTGT... | AGAAAAAAAAAAAAAAAAAAAAAAGTAGAAATGCTAACCACCTGCCAACCCCAACAGGTTCCTCTGACAATCAGATGTAATGGGTGGGACAAGCTATACCAATGGATGACATCACTATCTCATAACAAAAATATCAGTGCCAGAGAGAGTATTATAAGGAAACTGACACTCAGTAAGGTTTAATGAGTAAACTAGATTAGCAACTTCACATTCACTGAGTGATTTCACATCCAGTGTGGCATCTAGTCCACATTTTAAGTGTAAATCCCACTATGAATAACTTAAAGGAAATCATTTCATCATTTGTTCTGAACCTCTGT... |
Task1_train_42420 | Here is a mutation located on Chromosome 12. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AGGGTGGAGGTCCCCTCAAACACAGCCCCTCAGCTTCTAGGCTGCTTTGGAGGCCAGACAGGAAGAGTTCCATTCATTCAACCTGATCCCAGCAGCAGTAGCGGGATGAGAAACTCACCCCCAGGCCGGGGGTGCTTGGAGAGCGCTTGAGAGGATTTAAATGCCCTATACCCCACATCCCTAATCCTGGACCAACTAGAAACAGGGGGCCACCTTCAGGAAAATTAAGAGCAGTATTTTCCAGAGTGGGTGCTGCAGGATTTTACCCTGTAGCTGTTTTAAAAAGTAGTTTGGGCCGGGCACGGTGGCTCACGCCTGTA... | AGGGTGGAGGTCCCCTCAAACACAGCCCCTCAGCTTCTAGGCTGCTTTGGAGGCCAGACAGGAAGAGTTCCATTCATTCAACCTGATCCCAGCAGCAGTAGCGGGATGAGAAACTCACCCCCAGGCCGGGGGTGCTTGGAGAGCGCTTGAGAGGATTTAAATGCCCTATACCCCACATCCCTAATCCTGGACCAACTAGAAACAGGGGGCCACCTTCAGGAAAATTAAGAGCAGTATTTTCCAGAGTGGGTGCTGCAGGATTTTACCCTGTAGCTGTTTTAAAAAGTAGTTTGGGCCGGGCACGGTGGCTCACGCCTGTA... |
Task1_train_42421 | A variant on Chromosome 12 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TCAGCTCCCACTTGCCCCTGCTGTACTCATAGTTGAGCCCAAATGCCCCCACTGCAAAATCCCATAGCTGCAGTCCCTGCAGTGATTGAGAGAGTCCCACTCCCCTTGAACAAAGTCTTCCTTACCATGCTTTAACAAGGGTCATTGAATCTTTTTTTTTTTTTTTGAGACGGAGTCTTACTCTGTCACCCAGGCTGGAGTGCAGTAGCGTGATCTCAGCTCACTGCAACCTCCCTCCGCTTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCCAGTAGCTGGGACTACAGGCATGTGCCACCACACCTGACTAAT... | TCAGCTCCCACTTGCCCCTGCTGTACTCATAGTTGAGCCCAAATGCCCCCACTGCAAAATCCCATAGCTGCAGTCCCTGCAGTGATTGAGAGAGTCCCACTCCCCTTGAACAAAGTCTTCCTTACCATGCTTTAACAAGGGTCATTGAATCTTTTTTTTTTTTTTTGAGACGGAGTCTTACTCTGTCACCCAGGCTGGAGTGCAGTAGCGTGATCTCAGCTCACTGCAACCTCCCTCCGCTTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCCAGTAGCTGGGACTACAGGCATGTGCCACCACACCTGACTAAT... |
Task1_train_42422 | This sequence variant lies on Chromosome 12. Is it clinically significant, and what condition might it cause if any? | Benign | AGCTCCCACTTGCCCCTGCTGTACTCATAGTTGAGCCCAAATGCCCCCACTGCAAAATCCCATAGCTGCAGTCCCTGCAGTGATTGAGAGAGTCCCACTCCCCTTGAACAAAGTCTTCCTTACCATGCTTTAACAAGGGTCATTGAATCTTTTTTTTTTTTTTTGAGACGGAGTCTTACTCTGTCACCCAGGCTGGAGTGCAGTAGCGTGATCTCAGCTCACTGCAACCTCCCTCCGCTTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCCAGTAGCTGGGACTACAGGCATGTGCCACCACACCTGACTAATCT... | AGCTCCCACTTGCCCCTGCTGTACTCATAGTTGAGCCCAAATGCCCCCACTGCAAAATCCCATAGCTGCAGTCCCTGCAGTGATTGAGAGAGTCCCACTCCCCTTGAACAAAGTCTTCCTTACCATGCTTTAACAAGGGTCATTGAATCTTTTTTTTTTTTTTTGAGACGGAGTCTTACTCTGTCACCCAGGCTGGAGTGCAGTAGCGTGATCTCAGCTCACTGCAACCTCCCTCCGCTTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCCAGTAGCTGGGACTACAGGCATGTGCCACCACACCTGACTAATCT... |
Task1_train_42423 | Given this variant on Chromosome 12, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CACCCAAGGATGTACAAGACCCCCTGTTGTCCAAGAGGCAAAACTGAAGTCAACCTAACAGCCCATGAAAGAGGCTTCCTGGGGGGCCAGGGGCTGAGGGCAGACAGCTGAGGACCAGCCCCCATCCTGCACTGAGGGATGGAGAATTCCGGGAAGGCTGCCTGAAGGAGACAGCCTTGAAACCTTGAAGGATTCCGCTATCGTTTGTCCATCACATATTTATTGCCTGCACTGGACCTGCAGTTGGGATACTGCAGTGAACAAGACAGAGTCCACCCTGGAAAGTGGCCACAGGGGAAGGCAAGAGGCGATAGCTGGGG... | CACCCAAGGATGTACAAGACCCCCTGTTGTCCAAGAGGCAAAACTGAAGTCAACCTAACAGCCCATGAAAGAGGCTTCCTGGGGGGCCAGGGGCTGAGGGCAGACAGCTGAGGACCAGCCCCCATCCTGCACTGAGGGATGGAGAATTCCGGGAAGGCTGCCTGAAGGAGACAGCCTTGAAACCTTGAAGGATTCCGCTATCGTTTGTCCATCACATATTTATTGCCTGCACTGGACCTGCAGTTGGGATACTGCAGTGAACAAGACAGAGTCCACCCTGGAAAGTGGCCACAGGGGAAGGCAAGAGGCGATAGCTGGGG... |
Task1_train_42424 | Located on Chromosome 12, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | AAGCGCGCTCTGCGATGTTTACACAATGATGACATCACCTAAGGATGCATTTCTCAGACTGTATCCCCATTGTTAAGTGATGCTGACTGTATTCAAATTTTTGCTATTACAAATAATGTTGATGAATATTCTTGTAGTTATGCCCATGGTTATTTCCTTAAAAATCCCAAAATTATTGCTGGGTCAGATATTTAATCTTTCAGTTGTTCCAAGCGATTCTTTAGTATTATTGTACCTCTTATGTGTACAAGGTTGTTTTAATATGTTTTAATAGAATTTTATTCTAAGTACATTATATTTTACTGTGTTAATGTTGGGCA... | AAGCGCGCTCTGCGATGTTTACACAATGATGACATCACCTAAGGATGCATTTCTCAGACTGTATCCCCATTGTTAAGTGATGCTGACTGTATTCAAATTTTTGCTATTACAAATAATGTTGATGAATATTCTTGTAGTTATGCCCATGGTTATTTCCTTAAAAATCCCAAAATTATTGCTGGGTCAGATATTTAATCTTTCAGTTGTTCCAAGCGATTCTTTAGTATTATTGTACCTCTTATGTGTACAAGGTTGTTTTAATATGTTTTAATAGAATTTTATTCTAAGTACATTATATTTTACTGTGTTAATGTTGGGCA... |
Task1_train_42425 | An alteration has been detected on Chromosome 12. Is it pathogenic, and if so, what disease is involved? | Benign | TACAAATAATGTTGATGAATATTCTTGTAGTTATGCCCATGGTTATTTCCTTAAAAATCCCAAAATTATTGCTGGGTCAGATATTTAATCTTTCAGTTGTTCCAAGCGATTCTTTAGTATTATTGTACCTCTTATGTGTACAAGGTTGTTTTAATATGTTTTAATAGAATTTTATTCTAAGTACATTATATTTTACTGTGTTAATGTTGGGCATCTCAATATTAAACTGTTTCATAGTCACATATCTTGCATCTTTAAAACTTTGAACTAAGCCTAAATCGTTTCTGGATTTTCTGCAATATTTCTTTCAGAGTCCTGTT... | TACAAATAATGTTGATGAATATTCTTGTAGTTATGCCCATGGTTATTTCCTTAAAAATCCCAAAATTATTGCTGGGTCAGATATTTAATCTTTCAGTTGTTCCAAGCGATTCTTTAGTATTATTGTACCTCTTATGTGTACAAGGTTGTTTTAATATGTTTTAATAGAATTTTATTCTAAGTACATTATATTTTACTGTGTTAATGTTGGGCATCTCAATATTAAACTGTTTCATAGTCACATATCTTGCATCTTTAAAACTTTGAACTAAGCCTAAATCGTTTCTGGATTTTCTGCAATATTTCTTTCAGAGTCCTGTT... |
Task1_train_42426 | A mutation found on Chromosome 12 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AGGGTCACAGCAAAATGGAGCGGAAAGAATAGAGAGTTCCCACATACCCCAGGCCCTCATGTGCACACAGATGCCCAAGCTTTTTTATTTTACTTATATGAGTGCACTATGAATATGTTCTTAATGTAGAGAGTCAGTCAAGTCAGCCATGTGTTAAGAATAAAAAAGGAAAAACCCTTTTCCCCATTACCTTCCAACTCTCCTTTCTCAGATGTAACCACTATTAGCAGCTGCCGATGGTGGGGGGCTCTTTTCAGCACTGTCACTGTATATACTTTTACATAGACATTCATACAGTTGTTTCATTATTTTTTGCATGA... | AGGGTCACAGCAAAATGGAGCGGAAAGAATAGAGAGTTCCCACATACCCCAGGCCCTCATGTGCACACAGATGCCCAAGCTTTTTTATTTTACTTATATGAGTGCACTATGAATATGTTCTTAATGTAGAGAGTCAGTCAAGTCAGCCATGTGTTAAGAATAAAAAAGGAAAAACCCTTTTCCCCATTACCTTCCAACTCTCCTTTCTCAGATGTAACCACTATTAGCAGCTGCCGATGGTGGGGGGCTCTTTTCAGCACTGTCACTGTATATACTTTTACATAGACATTCATACAGTTGTTTCATTATTTTTTGCATGA... |
Task1_train_42427 | This variant is found on Chromosome 12. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TCGAATTGTTTTTTTGGTGGATTCTTTAGGTTTATCCAATTTTAAGATTATATCATCTGTAAACAAGGATAATTGGACTTCTTCCTTTCCAATTTGGATGTCCTTTATTTCTTCTCTAAATTGTTTTCATTGTTTTCTTCCTTCCTTCCTTCTTTCTTCCCATAATGGGGTCTCATTACGTTGCCCAGGCTGGTCTCCCTCCCTTCCTCTTTTTCTTCCTTCAGCAGAATTTTTTAAAAAGTTTTCTTTATTTTTTTTTCAGTTTGAAAGATTTCAAAAAAGTTGCAAGAATGATACAATTAATACCCATACGCCCTGCA... | TCGAATTGTTTTTTTGGTGGATTCTTTAGGTTTATCCAATTTTAAGATTATATCATCTGTAAACAAGGATAATTGGACTTCTTCCTTTCCAATTTGGATGTCCTTTATTTCTTCTCTAAATTGTTTTCATTGTTTTCTTCCTTCCTTCCTTCTTTCTTCCCATAATGGGGTCTCATTACGTTGCCCAGGCTGGTCTCCCTCCCTTCCTCTTTTTCTTCCTTCAGCAGAATTTTTTAAAAAGTTTTCTTTATTTTTTTTTCAGTTTGAAAGATTTCAAAAAAGTTGCAAGAATGATACAATTAATACCCATACGCCCTGCA... |
Task1_train_42428 | Here is a mutation located on Chromosome 12. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CGCCCAGCTAATTTTTGTATATTTAGTAGAGATGGGGTTTTGCCATGTCATCCAGGCTGGCCTGGAATTCCTGGGCTCACGCGATCCACCTGCCTTGGCTCCCCAGAGTGCTGGGATTACAGGCGTGTGCCACCATGCCTGACCCCATTCTTGACAGGGAATGGTGGGAACCTTCCCCAAATTCAAGTTCCCCAGTGCTGGCCAAGGGCAAGTCTTTTAATGGAAAGCAATTATGTCTGCTAATTGCTGTATTAGCTCCTGCTGCCCAGTTCCCGCATTTCCTGTTCAGTTGAAAAGCTTCCAGTGTTTAAACTCCAGAA... | CGCCCAGCTAATTTTTGTATATTTAGTAGAGATGGGGTTTTGCCATGTCATCCAGGCTGGCCTGGAATTCCTGGGCTCACGCGATCCACCTGCCTTGGCTCCCCAGAGTGCTGGGATTACAGGCGTGTGCCACCATGCCTGACCCCATTCTTGACAGGGAATGGTGGGAACCTTCCCCAAATTCAAGTTCCCCAGTGCTGGCCAAGGGCAAGTCTTTTAATGGAAAGCAATTATGTCTGCTAATTGCTGTATTAGCTCCTGCTGCCCAGTTCCCGCATTTCCTGTTCAGTTGAAAAGCTTCCAGTGTTTAAACTCCAGAA... |
Task1_train_42429 | This sequence change occurs on Chromosome 12. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GAAAAGCTGCTCTTTAGAGTAACTCGGGCCTCAGCTCGAATGCTGGATCTGTCCCCTTGCTTCCTGCTGTCCCTAGCCAAGTTCCTTCACCTCTCTGGGCCTCAGTTTCCTCTTCTGTAAAATAAGAATAATAACAGTACCTACCAAAAGTTGTTGGAAAAGTGTATGTATTCAGTGGGCGCTTAATAAGTGGAAACTTATGATTAAGAATGTCATTGTCTGTATCCTTTTGCCTTTGACCTCAAGAGCTATAAGGGAAGAAACATGACTGAACCAGAAGCAAATCCATCGTCTCTTTTTTAGATAAATCCATTGTCTCT... | GAAAAGCTGCTCTTTAGAGTAACTCGGGCCTCAGCTCGAATGCTGGATCTGTCCCCTTGCTTCCTGCTGTCCCTAGCCAAGTTCCTTCACCTCTCTGGGCCTCAGTTTCCTCTTCTGTAAAATAAGAATAATAACAGTACCTACCAAAAGTTGTTGGAAAAGTGTATGTATTCAGTGGGCGCTTAATAAGTGGAAACTTATGATTAAGAATGTCATTGTCTGTATCCTTTTGCCTTTGACCTCAAGAGCTATAAGGGAAGAAACATGACTGAACCAGAAGCAAATCCATCGTCTCTTTTTTAGATAAATCCATTGTCTCT... |
Task1_train_42430 | This variant is present on Chromosome 12. Is the change likely to result in a pathogenic outcome? | Benign | GGAGTCATTTTAACATTCCCATTGGTCTCTGGTGGGGGATTTTTCTCAATATGAAGCCAGTTTCATTCCTACTGATACAAGAGCTCTTTTTTTCCAATTTGCAGCTATCTGGGTCCTTATGAGAAAAAAAAAATTAGTTTTAGGCAATTCTGGTCGATCTAACTCCCTGTATTACTGACATTTTAAAACAAATTATTGAAGTGCCATTACACATTGCAGAAAATTAGAAAAGGAACCCCCCAAAAAAGTAATTTTGCAGCTTCTATCATTCTGGTATAGTTCCCTCTCATCTTCTGTCTTTATGTGGTTAATTTATAGTG... | GGAGTCATTTTAACATTCCCATTGGTCTCTGGTGGGGGATTTTTCTCAATATGAAGCCAGTTTCATTCCTACTGATACAAGAGCTCTTTTTTTCCAATTTGCAGCTATCTGGGTCCTTATGAGAAAAAAAAAATTAGTTTTAGGCAATTCTGGTCGATCTAACTCCCTGTATTACTGACATTTTAAAACAAATTATTGAAGTGCCATTACACATTGCAGAAAATTAGAAAAGGAACCCCCCAAAAAAGTAATTTTGCAGCTTCTATCATTCTGGTATAGTTCCCTCTCATCTTCTGTCTTTATGTGGTTAATTTATAGTG... |
Task1_train_42431 | A genomic variant on Chromosome 12 is under review. What is the biological outcome — benign or pathogenic? | Benign | CAGCCAGGGCCGGGCGTGGCAGCTCACACCTGTAATCCCAGCACGTTGGGAGGCCAAGGCGGGTGGATCACCTGCAGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGCGAAACCCCGTCTCTACTGAAAATACAAAAATTAGCTGGGCGTGGTGGCAGGCACCTGTAATCCCAGCTACTCGGGGGGCTGAAGCAGCAGAATTGCTTGAACCCAGAAGGTGGATGTTGCAGTGAGCCGAGATTGCGCCATTGCACTCCAGCCTGGGTGACAGAGCGAGACTCCATCTTCAAAATAAATAAAATAAAATAAATTATATTT... | CAGCCAGGGCCGGGCGTGGCAGCTCACACCTGTAATCCCAGCACGTTGGGAGGCCAAGGCGGGTGGATCACCTGCAGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGCGAAACCCCGTCTCTACTGAAAATACAAAAATTAGCTGGGCGTGGTGGCAGGCACCTGTAATCCCAGCTACTCGGGGGGCTGAAGCAGCAGAATTGCTTGAACCCAGAAGGTGGATGTTGCAGTGAGCCGAGATTGCGCCATTGCACTCCAGCCTGGGTGACAGAGCGAGACTCCATCTTCAAAATAAATAAAATAAAATAAATTATATTT... |
Task1_train_42432 | A genomic change on Chromosome 12 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GGAGGGAAGTGAATATGGATATATATGTATTTTAAAATATGATCTTGCTGTGGATATTGATTATAACCTGCCCCTTTTCACTTATTGTTTGAGAACTTTTTTTTTTTTTTTTTTGAGATGGAGTCTTGCTCTGTCACCCAGGCTGGAGTACAGTGGCTTGATCTCGGGTCACTGCAACCTCCGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTAAGTAGCTGGGATTACAGGCACCTGCCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAAC... | GGAGGGAAGTGAATATGGATATATATGTATTTTAAAATATGATCTTGCTGTGGATATTGATTATAACCTGCCCCTTTTCACTTATTGTTTGAGAACTTTTTTTTTTTTTTTTTTGAGATGGAGTCTTGCTCTGTCACCCAGGCTGGAGTACAGTGGCTTGATCTCGGGTCACTGCAACCTCCGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTAAGTAGCTGGGATTACAGGCACCTGCCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAAC... |
Task1_train_42433 | This alteration occurs on Chromosome 12. Is it associated with a disease or is it a benign variant? | Benign | AAGGGTTTTGTGCATTGATCCGTATCCATCTAGAGCCTGGAGACTCGATTCCTAGGGATTTATGGAGATTTGCGAGATTTATGCTTCATCTACTCGATGTAAATGCAGCTCTTAATTCTTTAGAAGAGCTATGGTGCTGCCGGTGGGAGGAAATGAAGTTATAAAGGAAACTTCCGCACTAAACTGATTTAGCAGATGGGCCTCCTTGCTAGCAAAACAAAGAGGGAACCAGAGGGGGCACCTAACGTCCGTGTGCCTGGATTCTTTCACTGTTCCCATGTACGCATGACCTGCCAGAGGAGCTACTGGGACCTAGACAA... | AAGGGTTTTGTGCATTGATCCGTATCCATCTAGAGCCTGGAGACTCGATTCCTAGGGATTTATGGAGATTTGCGAGATTTATGCTTCATCTACTCGATGTAAATGCAGCTCTTAATTCTTTAGAAGAGCTATGGTGCTGCCGGTGGGAGGAAATGAAGTTATAAAGGAAACTTCCGCACTAAACTGATTTAGCAGATGGGCCTCCTTGCTAGCAAAACAAAGAGGGAACCAGAGGGGGCACCTAACGTCCGTGTGCCTGGATTCTTTCACTGTTCCCATGTACGCATGACCTGCCAGAGGAGCTACTGGGACCTAGACAA... |
Task1_train_42434 | A genetic alteration is present on Chromosome 12. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TTAGGATCACCAGATACTAATGGGGAGCTGAGACTGAAACCCAGGTTGGCAAGTCTTTGTCAAGACCCCATCTTGGGAGGACAAGGGTCCAGGGAAGATACCTCTCTCTCCCCCAGGCTTGAGTTTCACTCTGAAGTCACAGAAGCATGGCAGAGATAAGCAAGCTAAGCCCTGGGTGAGGAAGTGACTTTCTCAAAGTAACATAGCAAATCAACGACCAAGTCAAGATGGTGGGAGTCCCCAACAAGCTGCCTCCTACACATCTTCAGGTCTCGACTTAAATGTCACTTCTTCAGGGAAGCCCTCCTTGACCACATAAC... | TTAGGATCACCAGATACTAATGGGGAGCTGAGACTGAAACCCAGGTTGGCAAGTCTTTGTCAAGACCCCATCTTGGGAGGACAAGGGTCCAGGGAAGATACCTCTCTCTCCCCCAGGCTTGAGTTTCACTCTGAAGTCACAGAAGCATGGCAGAGATAAGCAAGCTAAGCCCTGGGTGAGGAAGTGACTTTCTCAAAGTAACATAGCAAATCAACGACCAAGTCAAGATGGTGGGAGTCCCCAACAAGCTGCCTCCTACACATCTTCAGGTCTCGACTTAAATGTCACTTCTTCAGGGAAGCCCTCCTTGACCACATAAC... |
Task1_train_42435 | A variant found on Chromosome 12 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | AGCATGGCAGAGATAAGCAAGCTAAGCCCTGGGTGAGGAAGTGACTTTCTCAAAGTAACATAGCAAATCAACGACCAAGTCAAGATGGTGGGAGTCCCCAACAAGCTGCCTCCTACACATCTTCAGGTCTCGACTTAAATGTCACTTCTTCAGGGAAGCCCTCCTTGACCACATAACGCATGGCCAGAGGCAGGCACATGGTGGGTGAGCTTACCTTCACTGTCGGTGAGCACTTCCATGCGCCCGCTGAACATGGCCTTCAGCATGGTGTCCTGCTTGGTCAGCGTCTGCATGGTGGTATAGTAGAGGGCTCCACCCAC... | AGCATGGCAGAGATAAGCAAGCTAAGCCCTGGGTGAGGAAGTGACTTTCTCAAAGTAACATAGCAAATCAACGACCAAGTCAAGATGGTGGGAGTCCCCAACAAGCTGCCTCCTACACATCTTCAGGTCTCGACTTAAATGTCACTTCTTCAGGGAAGCCCTCCTTGACCACATAACGCATGGCCAGAGGCAGGCACATGGTGGGTGAGCTTACCTTCACTGTCGGTGAGCACTTCCATGCGCCCGCTGAACATGGCCTTCAGCATGGTGTCCTGCTTGGTCAGCGTCTGCATGGTGGTATAGTAGAGGGCTCCACCCAC... |
Task1_train_42436 | A mutation on Chromosome 12 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CCCAATTTCAGCCTTCAGTTTTCTCAGAAATCCCACGCAGAATAATTTCTAGGAATTTGAGCACGTTGGTGGGGTTGTGCTTTTGTTCTGGATGCACACGGAGACCTGTCTGAATGAGTGGATCTATCTGTGTCTAGCCCTGTGATTGCTGCACAGTTCTCAGACAATCTGATTCGGCCGTTCCTCATCCACATCATGTCTGTGCCTGCTCTGGTGACTCATCTCAGCACAGTGACCCCTGAGGTAAGCAGGCTCTGTGAGTTCCCCGTGAAAACCCAATTGTGTTTTTCTTTTCTTCTTAAACATTAGAAAGTAAAATG... | CCCAATTTCAGCCTTCAGTTTTCTCAGAAATCCCACGCAGAATAATTTCTAGGAATTTGAGCACGTTGGTGGGGTTGTGCTTTTGTTCTGGATGCACACGGAGACCTGTCTGAATGAGTGGATCTATCTGTGTCTAGCCCTGTGATTGCTGCACAGTTCTCAGACAATCTGATTCGGCCGTTCCTCATCCACATCATGTCTGTGCCTGCTCTGGTGACTCATCTCAGCACAGTGACCCCTGAGGTAAGCAGGCTCTGTGAGTTCCCCGTGAAAACCCAATTGTGTTTTTCTTTTCTTCTTAAACATTAGAAAGTAAAATG... |
Task1_train_42437 | This variant is found on Chromosome 12. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | ACAGGACTTGGCAACAGGTGAACGGCCTTGTTTCAAAGATTGTCACTTTAGGATGTTGTATTTACTCAAAAAGCTTTCCTTATCCTTTGGAGGCTGTGCTTTCCCATGGCTAGGCATGCAGGGCTGCTGTGTTATTTTATATATATATATATATTCCAGGAAGATTTTGAGATTTTGAGGTGTAGACAGAATTGAGTGATTCGCTGCAAGCTCTTTGAACATACTCCCTGACCGAGCCTTAGTGATTGCGTTTTCAGGGTTTTTTTTTTTTTTTTTTTTTTTTTGTGACGGAGTCTCACTCTATCAGCCAGGCTGGAGTG... | ACAGGACTTGGCAACAGGTGAACGGCCTTGTTTCAAAGATTGTCACTTTAGGATGTTGTATTTACTCAAAAAGCTTTCCTTATCCTTTGGAGGCTGTGCTTTCCCATGGCTAGGCATGCAGGGCTGCTGTGTTATTTTATATATATATATATATTCCAGGAAGATTTTGAGATTTTGAGGTGTAGACAGAATTGAGTGATTCGCTGCAAGCTCTTTGAACATACTCCCTGACCGAGCCTTAGTGATTGCGTTTTCAGGGTTTTTTTTTTTTTTTTTTTTTTTTTGTGACGGAGTCTCACTCTATCAGCCAGGCTGGAGTG... |
Task1_train_42438 | This sequence change occurs on Chromosome 12. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GGCTCAACAGGCTCTGACCTGGGCCTAAACCTTGAGCAGCATTTCACATCCTGCCACCGCTCAACCTGAACCTGCACAGGCTCGGCCGGCAGTGGAGATGACAAATCCATCACAGGTGGGTTTAAACAGGCCATCGGCCCCCTTTCCACCAGCACATCGCAGGACGGCCTGGCCAAGGAGGGATCAAGGATGGCTGGTGAGTTGAGGGAGCCACCTGGCCTACACCACACCCCAGCCAGCCAGCTTTTGTACCACTGGACCTGGGTCTGGGTGGGGTGAAGTTGGGGTGGTCTGCCTCTAGCCTTCAAAGGAAGTGGGGG... | GGCTCAACAGGCTCTGACCTGGGCCTAAACCTTGAGCAGCATTTCACATCCTGCCACCGCTCAACCTGAACCTGCACAGGCTCGGCCGGCAGTGGAGATGACAAATCCATCACAGGTGGGTTTAAACAGGCCATCGGCCCCCTTTCCACCAGCACATCGCAGGACGGCCTGGCCAAGGAGGGATCAAGGATGGCTGGTGAGTTGAGGGAGCCACCTGGCCTACACCACACCCCAGCCAGCCAGCTTTTGTACCACTGGACCTGGGTCTGGGTGGGGTGAAGTTGGGGTGGTCTGCCTCTAGCCTTCAAAGGAAGTGGGGG... |
Task1_train_42439 | Mutation context: Chromosome 12. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GGGCCTAAACCTTGAGCAGCATTTCACATCCTGCCACCGCTCAACCTGAACCTGCACAGGCTCGGCCGGCAGTGGAGATGACAAATCCATCACAGGTGGGTTTAAACAGGCCATCGGCCCCCTTTCCACCAGCACATCGCAGGACGGCCTGGCCAAGGAGGGATCAAGGATGGCTGGTGAGTTGAGGGAGCCACCTGGCCTACACCACACCCCAGCCAGCCAGCTTTTGTACCACTGGACCTGGGTCTGGGTGGGGTGAAGTTGGGGTGGTCTGCCTCTAGCCTTCAAAGGAAGTGGGGGCCTGACCCTTAATTCCCAAT... | GGGCCTAAACCTTGAGCAGCATTTCACATCCTGCCACCGCTCAACCTGAACCTGCACAGGCTCGGCCGGCAGTGGAGATGACAAATCCATCACAGGTGGGTTTAAACAGGCCATCGGCCCCCTTTCCACCAGCACATCGCAGGACGGCCTGGCCAAGGAGGGATCAAGGATGGCTGGTGAGTTGAGGGAGCCACCTGGCCTACACCACACCCCAGCCAGCCAGCTTTTGTACCACTGGACCTGGGTCTGGGTGGGGTGAAGTTGGGGTGGTCTGCCTCTAGCCTTCAAAGGAAGTGGGGGCCTGACCCTTAATTCCCAAT... |
Task1_train_42440 | A variant was discovered on Chromosome 12. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TAGCTGCTGGGGTTACAGGCATGGACCACCATACTCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCACATTGGCCAGGCTAGTCTCAAATTCCTGGCCTCAGATGATTAGCCCAACAGGGCCTCCCAAAGTGCCGGGATTACAGGCATGAGCCACCGCGCCTGGTATATTATACTTTAAAGTGGCTGCAAAGAATTTGGAAGAACTTTAAAATGGTGTATGCCATGAGTATTTCTTTGCATTTTTCACCTGTCCCCACCCTACCTTTGTCTCCCGTTTTGGTGTAAATCTTGGGGATCCTGGGTGTCTTCG... | TAGCTGCTGGGGTTACAGGCATGGACCACCATACTCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCACATTGGCCAGGCTAGTCTCAAATTCCTGGCCTCAGATGATTAGCCCAACAGGGCCTCCCAAAGTGCCGGGATTACAGGCATGAGCCACCGCGCCTGGTATATTATACTTTAAAGTGGCTGCAAAGAATTTGGAAGAACTTTAAAATGGTGTATGCCATGAGTATTTCTTTGCATTTTTCACCTGTCCCCACCCTACCTTTGTCTCCCGTTTTGGTGTAAATCTTGGGGATCCTGGGTGTCTTCG... |
Task1_train_42441 | Here’s a variant located on Chromosome 12. What is the predicted biological effect — harmless or disease-causing? | Benign | AGCTTGACAAGCAAGGGGATTCCCCGCTCTGAGCCTCAGTTTTTCTAAGAAATGGGGATCACGATAGTACTTAGCTCATAGTACACCTGAATCTTAGCGTAAGGTAATCTACGTAAAGCCTTAAGCGGAGGATAATTTTGCGTTATGTATAAAAGTGTAAATTGCACACACCTATAGACCCTGCAAGCTCCTTTCTAGGACTCTGTCCTGCAGAAATACTCATTTAAGTGTGCAAAACGAGGCGTACTGGGTGTTTTCTGCAGCCTTGTTTATAATTGTGACACATTGGAAACAGCCTAAATGTCCAGCAAAGAGTTCTT... | AGCTTGACAAGCAAGGGGATTCCCCGCTCTGAGCCTCAGTTTTTCTAAGAAATGGGGATCACGATAGTACTTAGCTCATAGTACACCTGAATCTTAGCGTAAGGTAATCTACGTAAAGCCTTAAGCGGAGGATAATTTTGCGTTATGTATAAAAGTGTAAATTGCACACACCTATAGACCCTGCAAGCTCCTTTCTAGGACTCTGTCCTGCAGAAATACTCATTTAAGTGTGCAAAACGAGGCGTACTGGGTGTTTTCTGCAGCCTTGTTTATAATTGTGACACATTGGAAACAGCCTAAATGTCCAGCAAAGAGTTCTT... |
Task1_train_42442 | A mutation on Chromosome 12 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TCTTGGCAGCCATCATGAGGGGCGAGAGGCCGTCGTTGTTGAGCACGGCCTCCAGGTTGCTGTCGGGGAAGAGGCGGGCACACTTGAGCAGCAGCAGGTCGTACATCTTGGTAACAAACTTGGTGTTCTCACGGGTGTTGTCAGCAATGGCCACCAGCGCATGCAGCACTGTGTTGCCTCGCGAGTCCTGGCGCCGCATGTCCGCCTTCTTGTGGGGGTTCTCCGTCAGGTAGTTGACAATGTGGGGCTGGTTGGTGCAGGCAGCCAGCGACAGGGGCAGCTCCCCTGCGGGCCAGGGTGAAGGGTGGGAGGTCAGCGAA... | TCTTGGCAGCCATCATGAGGGGCGAGAGGCCGTCGTTGTTGAGCACGGCCTCCAGGTTGCTGTCGGGGAAGAGGCGGGCACACTTGAGCAGCAGCAGGTCGTACATCTTGGTAACAAACTTGGTGTTCTCACGGGTGTTGTCAGCAATGGCCACCAGCGCATGCAGCACTGTGTTGCCTCGCGAGTCCTGGCGCCGCATGTCCGCCTTCTTGTGGGGGTTCTCCGTCAGGTAGTTGACAATGTGGGGCTGGTTGGTGCAGGCAGCCAGCGACAGGGGCAGCTCCCCTGCGGGCCAGGGTGAAGGGTGGGAGGTCAGCGAA... |
Task1_train_42443 | A genomic variant on Chromosome 12 is under review. What is the biological outcome — benign or pathogenic? | Benign | CAGCCATCATGAGGGGCGAGAGGCCGTCGTTGTTGAGCACGGCCTCCAGGTTGCTGTCGGGGAAGAGGCGGGCACACTTGAGCAGCAGCAGGTCGTACATCTTGGTAACAAACTTGGTGTTCTCACGGGTGTTGTCAGCAATGGCCACCAGCGCATGCAGCACTGTGTTGCCTCGCGAGTCCTGGCGCCGCATGTCCGCCTTCTTGTGGGGGTTCTCCGTCAGGTAGTTGACAATGTGGGGCTGGTTGGTGCAGGCAGCCAGCGACAGGGGCAGCTCCCCTGCGGGCCAGGGTGAAGGGTGGGAGGTCAGCGAAGGGGGC... | CAGCCATCATGAGGGGCGAGAGGCCGTCGTTGTTGAGCACGGCCTCCAGGTTGCTGTCGGGGAAGAGGCGGGCACACTTGAGCAGCAGCAGGTCGTACATCTTGGTAACAAACTTGGTGTTCTCACGGGTGTTGTCAGCAATGGCCACCAGCGCATGCAGCACTGTGTTGCCTCGCGAGTCCTGGCGCCGCATGTCCGCCTTCTTGTGGGGGTTCTCCGTCAGGTAGTTGACAATGTGGGGCTGGTTGGTGCAGGCAGCCAGCGACAGGGGCAGCTCCCCTGCGGGCCAGGGTGAAGGGTGGGAGGTCAGCGAAGGGGGC... |
Task1_train_42444 | A mutation on Chromosome 12 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GGGCCAGGCACGGTGGCTCACGCTTGTAATCCCAGCACTTTGGGAGGCCAAAGCAGGTAGATCACTTGAGATCAGGAGTTCAAGACCAGCCTGACCAACATGGTGAAACCCTGTCTCTACTAAAAATACAGTAATTGGCCAGACATGGTGGCACATGCCTGTAATCCCAGCTACTCAGGAGACTGAGGTACTAGAATCGATTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCGAGATCGCACCACTGCACTCTAGCCTGGGCAACAGAGCGAGACCCATCTCAAAAATAAAAAAAATGAAAAACTTCCAACAGTACTTTC... | GGGCCAGGCACGGTGGCTCACGCTTGTAATCCCAGCACTTTGGGAGGCCAAAGCAGGTAGATCACTTGAGATCAGGAGTTCAAGACCAGCCTGACCAACATGGTGAAACCCTGTCTCTACTAAAAATACAGTAATTGGCCAGACATGGTGGCACATGCCTGTAATCCCAGCTACTCAGGAGACTGAGGTACTAGAATCGATTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCGAGATCGCACCACTGCACTCTAGCCTGGGCAACAGAGCGAGACCCATCTCAAAAATAAAAAAAATGAAAAACTTCCAACAGTACTTTC... |
Task1_train_42445 | A genomic change on Chromosome 12 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GCTATTTTAATGAAACATTACAGTTCAATTTCAGAACTGCTCAGGAGACTTTTTTTTTTTAAGACAATCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGTGCAATCTCGGCTTACTGCAACCTCCACTTCCCAGGTTCAAGGGATTCTTGATTCTCGTGCCTCAGCCTTCCAAGTATCTGGGATTACAGGCATGCGCCACCACCCGCCGCTAATTTTTGTATTTTTAGTAGAGACAGGTTTTGCCATGTTGGCCAGGCTGGTCTCAAATTCCTGGGCTCAAGTGATCCACCCACCTTGGCCTTCCAAAGTGCTGGGATT... | GCTATTTTAATGAAACATTACAGTTCAATTTCAGAACTGCTCAGGAGACTTTTTTTTTTTAAGACAATCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGTGCAATCTCGGCTTACTGCAACCTCCACTTCCCAGGTTCAAGGGATTCTTGATTCTCGTGCCTCAGCCTTCCAAGTATCTGGGATTACAGGCATGCGCCACCACCCGCCGCTAATTTTTGTATTTTTAGTAGAGACAGGTTTTGCCATGTTGGCCAGGCTGGTCTCAAATTCCTGGGCTCAAGTGATCCACCCACCTTGGCCTTCCAAAGTGCTGGGATT... |
Task1_train_42446 | This alteration on Chromosome 12 may affect genome function. Does it lead to a disease or is it benign? | Benign | CTTGTAATTCTGTACTTTTTGAGATGTGCTTCATCATTTTCTAGCACTGAAGCAGTATCATATTTTTCCTGAAGGATTACCTGTGTGTCAGTAGTCTCGGATGAAGGTAGTGAAGTGGATTTGAATCCCACTTCCTCCACAAAGGGTACCATCTCCCTAAACTCTCTCTGGGTCTCTAGTGAAACAGAAAATGAAGGACAGGACAGACCTGTGTAAGCAGTAGGCTTTGTGTGTGTGTGTGTGACTCTATGTTGCCCAAGTCGGAGTGCAGTGGCTGTTCCCCGGCATGATCATATTGCACCCTCAAACTCCTGGGTTCA... | CTTGTAATTCTGTACTTTTTGAGATGTGCTTCATCATTTTCTAGCACTGAAGCAGTATCATATTTTTCCTGAAGGATTACCTGTGTGTCAGTAGTCTCGGATGAAGGTAGTGAAGTGGATTTGAATCCCACTTCCTCCACAAAGGGTACCATCTCCCTAAACTCTCTCTGGGTCTCTAGTGAAACAGAAAATGAAGGACAGGACAGACCTGTGTAAGCAGTAGGCTTTGTGTGTGTGTGTGTGACTCTATGTTGCCCAAGTCGGAGTGCAGTGGCTGTTCCCCGGCATGATCATATTGCACCCTCAAACTCCTGGGTTCA... |
Task1_train_42447 | A genomic change on Chromosome 12 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GACTATAGGCATGTGCCACCACACCCAGCTAATTTTTTGTATTTTTTTTTGTAGAGACAGGGTTTCACCATGTTGCCCAGGCTGGTCTCAAACTTCTGGGCTGAAGCCATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGTCACCACATCGGGCCTTTAGTTTTTTTTTTTGTTTTTTTTTAGGGGTAATATAGTGTTTTCACAGGAAAGTCTATATTCACTTCCTAGAACTTTTGCTCAGATATAGGGATAGCCATTGCTTTCTTGCTTTCTTTTTTTTTTTTTTTTTTGTTGTTTTTTTTTTGT... | GACTATAGGCATGTGCCACCACACCCAGCTAATTTTTTGTATTTTTTTTTGTAGAGACAGGGTTTCACCATGTTGCCCAGGCTGGTCTCAAACTTCTGGGCTGAAGCCATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGTCACCACATCGGGCCTTTAGTTTTTTTTTTTGTTTTTTTTTAGGGGTAATATAGTGTTTTCACAGGAAAGTCTATATTCACTTCCTAGAACTTTTGCTCAGATATAGGGATAGCCATTGCTTTCTTGCTTTCTTTTTTTTTTTTTTTTTTGTTGTTTTTTTTTTGT... |
Task1_train_42448 | Given this context: Chromosome 12 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CTAACAAAACCCTTCTGGATGCAACTTTCTTTACTTTTTAAATACACAGAGACTGCAAATAGTTTGTGCAAAATAAATACCCCGCCACTTGCCACTCATGCTTCTGTGTTTTATCATAGCATGATGATTTCTCCTTAAATAGAGACTCCGTCCAGACCCCCCACCCCGCCCCCACCGCGTCTACCAAAGAATTCTGTTTTGTCAAGTTAGGGTAGTTAAGGCATTCTGACATGTAATTAAAGGTGATTCAAAATAGATTATCTAACATTATGCCAATTTAGGAATAGTAGATAAATTACTGAACGGCTTACAAATGAATA... | CTAACAAAACCCTTCTGGATGCAACTTTCTTTACTTTTTAAATACACAGAGACTGCAAATAGTTTGTGCAAAATAAATACCCCGCCACTTGCCACTCATGCTTCTGTGTTTTATCATAGCATGATGATTTCTCCTTAAATAGAGACTCCGTCCAGACCCCCCACCCCGCCCCCACCGCGTCTACCAAAGAATTCTGTTTTGTCAAGTTAGGGTAGTTAAGGCATTCTGACATGTAATTAAAGGTGATTCAAAATAGATTATCTAACATTATGCCAATTTAGGAATAGTAGATAAATTACTGAACGGCTTACAAATGAATA... |
Task1_train_42449 | A mutation located on Chromosome 12 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | ATTAGTGCCTTGGCTGCACTGAACTTTCACTTAAAGAGAGGCCAAAGGTCTATCTTACTAAATGTGACTATGTTAAGACCCTTCTCTGTTGACCTGAATTCTAAAAACCCAGGATTCCTCCTGTGTTGAATTGGAGGTGGAAAGCTATTGAGGGAGGGGTTATGCTCACTTCTTAGGAGTCATATGTAGGGATAATTAACATTTTTTTCAGAAAATGATTAATTCTAGAATTACACATTTAGTGGAAATATTTTATAATCTAATTTGACGTTTGGCTGGCGCCGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGTC... | ATTAGTGCCTTGGCTGCACTGAACTTTCACTTAAAGAGAGGCCAAAGGTCTATCTTACTAAATGTGACTATGTTAAGACCCTTCTCTGTTGACCTGAATTCTAAAAACCCAGGATTCCTCCTGTGTTGAATTGGAGGTGGAAAGCTATTGAGGGAGGGGTTATGCTCACTTCTTAGGAGTCATATGTAGGGATAATTAACATTTTTTTCAGAAAATGATTAATTCTAGAATTACACATTTAGTGGAAATATTTTATAATCTAATTTGACGTTTGGCTGGCGCCGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGTC... |
Task1_train_42450 | A mutation is present on Chromosome 12. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TCAAGCATTTCTCCTGCCCCAGCCTCCCAAGTAGCTGGGACTACAGGCGCCCGCCACCACAGCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCACGTTGGCCAGGCTGGTCTCTAACTCCTGACCTCAAGTAATCCACCTGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCATGAGCCACCGCGCGTGGCTGGTGCTGGGATTTGAACCCACATTCCAGAATCTGTGTTCTTAGCCATCCTTGCTAGAGATAAGCAGTAACAGGCTTCTTGGTTACTTCCCCACCATCCCCACATCCCAATTCTGATT... | TCAAGCATTTCTCCTGCCCCAGCCTCCCAAGTAGCTGGGACTACAGGCGCCCGCCACCACAGCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCACGTTGGCCAGGCTGGTCTCTAACTCCTGACCTCAAGTAATCCACCTGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCATGAGCCACCGCGCGTGGCTGGTGCTGGGATTTGAACCCACATTCCAGAATCTGTGTTCTTAGCCATCCTTGCTAGAGATAAGCAGTAACAGGCTTCTTGGTTACTTCCCCACCATCCCCACATCCCAATTCTGATT... |
Task1_train_42451 | A variant on Chromosome 12 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GTCCAGGCTGAGGTTTCGACTGAAGCAGGGGTTGTCCTGCGCCCATGTGCCCACACGCTGCAACCTGGCTGGAGCCTCTGGCATAGGACACCCATACCACCAGGTAGCTGTGGCGGACCCCGGCTCTGATACTTGGCAGGCTTGGGTTGAGATTGTGGCTCTAGGCCTGGGCGGCTCTCAAGGGCTGCTGTGGGGAGTTGGGGAAGAACCCCTGGGTTGTGCTCAGCCAGCAGGCAGGTGGCAGCCAGGCTGGCTGTGGGTGAGGAGGGGAATCCTCTTTTCACCACTGCCTGCCTGCTCAGCAGTTCTTCAGCTGCTGG... | GTCCAGGCTGAGGTTTCGACTGAAGCAGGGGTTGTCCTGCGCCCATGTGCCCACACGCTGCAACCTGGCTGGAGCCTCTGGCATAGGACACCCATACCACCAGGTAGCTGTGGCGGACCCCGGCTCTGATACTTGGCAGGCTTGGGTTGAGATTGTGGCTCTAGGCCTGGGCGGCTCTCAAGGGCTGCTGTGGGGAGTTGGGGAAGAACCCCTGGGTTGTGCTCAGCCAGCAGGCAGGTGGCAGCCAGGCTGGCTGTGGGTGAGGAGGGGAATCCTCTTTTCACCACTGCCTGCCTGCTCAGCAGTTCTTCAGCTGCTGG... |
Task1_train_42452 | Consider this mutation on Chromosome 12. Is this a benign change or a disease-causing variant? | Benign | CAAAGTGCTGGGATTACAGGCGTGAGTCACTGTGCCTGGCCTTTTTAACAAATATTTTTGATCCAAGGTTGGCTGAATCCATGAATATGGAACCCACAGATGCAGAGGACCAACTGTACTTTTACAATGAATTATATTAGACTGGATAAAAGGAGTTCTAATCTATTTCTCTAAATCATCCTGACTAAACATGATCTAAGCAATGTTACTTTGACAATCATTTATCCACATTTTAACTTCATGGAATTACTTTATTCTACCCCCAAGGCAGTTTATCCCCAATAATCTAATAACTTACAACAACTGATGTAAGTATATGA... | CAAAGTGCTGGGATTACAGGCGTGAGTCACTGTGCCTGGCCTTTTTAACAAATATTTTTGATCCAAGGTTGGCTGAATCCATGAATATGGAACCCACAGATGCAGAGGACCAACTGTACTTTTACAATGAATTATATTAGACTGGATAAAAGGAGTTCTAATCTATTTCTCTAAATCATCCTGACTAAACATGATCTAAGCAATGTTACTTTGACAATCATTTATCCACATTTTAACTTCATGGAATTACTTTATTCTACCCCCAAGGCAGTTTATCCCCAATAATCTAATAACTTACAACAACTGATGTAAGTATATGA... |
Task1_train_42453 | A genomic change on Chromosome 12 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GAAGGGGAAGGGGGGGCGGGGCGTGTAAAGTCAAATAACCGACTGTTTCCGCCCCCTTTGAAGGCAGCAGAATTCCTTAAAAACCAGCTGATTCCTCTTGATGGGGAATTTCTGCTGTAAATAAAAATTCTTTGGAAATGGGTTGCTGAAAATGTGTTTTCAAAAAGAAAACTCGGGTGAATGAAAAATCCTCTTATTCCACCTTCCAAAGCCCAAGATGCCTATTTAAGGAGGACGCCGGTCACCCGCCGTCAAGCCGGCGGCCTAGGCCTAAAGAAGGCACAGTAGTGCCTACAACACGGATGGACTTGAGGCACAAG... | GAAGGGGAAGGGGGGGCGGGGCGTGTAAAGTCAAATAACCGACTGTTTCCGCCCCCTTTGAAGGCAGCAGAATTCCTTAAAAACCAGCTGATTCCTCTTGATGGGGAATTTCTGCTGTAAATAAAAATTCTTTGGAAATGGGTTGCTGAAAATGTGTTTTCAAAAAGAAAACTCGGGTGAATGAAAAATCCTCTTATTCCACCTTCCAAAGCCCAAGATGCCTATTTAAGGAGGACGCCGGTCACCCGCCGTCAAGCCGGCGGCCTAGGCCTAAAGAAGGCACAGTAGTGCCTACAACACGGATGGACTTGAGGCACAAG... |
Task1_train_42454 | Here is a genetic alteration on Chromosome 12. Based on the data, is it a benign variant or a cause of disease? | Benign | ATTTCCACCTTAAAATTTCTACCCATCTGCCCAGAAATCTTTCCTTGGATTTCCAATAGCCAGCCCTTTCTCATTCCTCAGGGGTCTCAGCTTAAATGTTACCTCCTGAGATTCCTTCCTTAATCATCTAATACGAAGAAGTCCCCACATCCAGTTATTCTCTTACCTCAGCATCCTGTTTATGTTCTTCTTAGCATCAGACTCGGGCTTTTTCCTGTTTATTACCTACTTCGTTTTCCTGAAAGATCCATGTGCCGGTACCATGTGTTGTTCCTACTGTTTCTCCAATGTCTAGTAGATTTGGCACATACTGATGTGCA... | ATTTCCACCTTAAAATTTCTACCCATCTGCCCAGAAATCTTTCCTTGGATTTCCAATAGCCAGCCCTTTCTCATTCCTCAGGGGTCTCAGCTTAAATGTTACCTCCTGAGATTCCTTCCTTAATCATCTAATACGAAGAAGTCCCCACATCCAGTTATTCTCTTACCTCAGCATCCTGTTTATGTTCTTCTTAGCATCAGACTCGGGCTTTTTCCTGTTTATTACCTACTTCGTTTTCCTGAAAGATCCATGTGCCGGTACCATGTGTTGTTCCTACTGTTTCTCCAATGTCTAGTAGATTTGGCACATACTGATGTGCA... |
Task1_train_42455 | Assess the clinical impact of this variant found on Chromosome 12. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CTGCTTTTGTATGAGGCAGTTATGTAACTTACTATCCCCTGGCTAATTATTCTAATTGTATATCATCCTGATGATATCAAATGAGTATCTGAAAACTTCATGAGCCACTTAGCACTTTAGCCCCAGTTAGACATAGCATAAATGCAAATTTATGGCCAAATGTAGAATTTAAAAAAGAAAATTATTTTATTATTTGGAAAATTAAATCAAAGCATATGTTCTATGTTTCAGAGTGTCATCCTAACTATGTAAAGGATATATTTGGCACATATGAGTTTTCTGGCCATAGGGGATTGATGAAGCCTATACTAGTTGTAGAG... | CTGCTTTTGTATGAGGCAGTTATGTAACTTACTATCCCCTGGCTAATTATTCTAATTGTATATCATCCTGATGATATCAAATGAGTATCTGAAAACTTCATGAGCCACTTAGCACTTTAGCCCCAGTTAGACATAGCATAAATGCAAATTTATGGCCAAATGTAGAATTTAAAAAAGAAAATTATTTTATTATTTGGAAAATTAAATCAAAGCATATGTTCTATGTTTCAGAGTGTCATCCTAACTATGTAAAGGATATATTTGGCACATATGAGTTTTCTGGCCATAGGGGATTGATGAAGCCTATACTAGTTGTAGAG... |
Task1_train_42456 | Chromosome 12 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GGCCTTATTCACAGTGTTTCAAATTTAGAAAGGGAGGAAAGAAAGCAGAGGAGCCTAATGGAAACTGAATTGAAGAGATTTTTACCTTTAAAAGACAATTAGCCAAAACTATATGCATCAGGTATTTGGTAGTGCTCAGTAACTATATGAAACATGACTTTAACAACATAAGGCCGATTATTGCTTTGTTTAATCCTTGCCATAATCCTATGAAGTAGGCATTATTATCATTTCCATTTACAGATAAAGAGATTGAAGCCTAGAGAGGTTAGGTAACTTTCCCAAGGTCAAAAGACAAGAACAGAAGCTAGGGCTTGAAA... | GGCCTTATTCACAGTGTTTCAAATTTAGAAAGGGAGGAAAGAAAGCAGAGGAGCCTAATGGAAACTGAATTGAAGAGATTTTTACCTTTAAAAGACAATTAGCCAAAACTATATGCATCAGGTATTTGGTAGTGCTCAGTAACTATATGAAACATGACTTTAACAACATAAGGCCGATTATTGCTTTGTTTAATCCTTGCCATAATCCTATGAAGTAGGCATTATTATCATTTCCATTTACAGATAAAGAGATTGAAGCCTAGAGAGGTTAGGTAACTTTCCCAAGGTCAAAAGACAAGAACAGAAGCTAGGGCTTGAAA... |
Task1_train_42457 | A genomic change on Chromosome 12 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TAAATCACAAATGGATGTAAGTGGATAATTAGTTCATGCTTTCTATGAACAAAGGTAGCCATGAAGACAAATAATTAAAAAAAAGTTACTACATTCTAGCTATAAACTGTAGCCTCATAGAGGCTCTGAGCCTGAGACTTGCTTCCCACTTAAAAAGGCAACTAGCAAGTGAAAGACAAGTGTTAAAGTCATATGAGCACTTTCTCCTTGAAGTACATAAGGTTGGAAAGGAGATTGAAATGGGAATGCCTTTCTTATTATTTAATATCACCCTGTCATTTACTGTCTGATTAATTTTTGTTATAATTTCTATTAAATAA... | TAAATCACAAATGGATGTAAGTGGATAATTAGTTCATGCTTTCTATGAACAAAGGTAGCCATGAAGACAAATAATTAAAAAAAAGTTACTACATTCTAGCTATAAACTGTAGCCTCATAGAGGCTCTGAGCCTGAGACTTGCTTCCCACTTAAAAAGGCAACTAGCAAGTGAAAGACAAGTGTTAAAGTCATATGAGCACTTTCTCCTTGAAGTACATAAGGTTGGAAAGGAGATTGAAATGGGAATGCCTTTCTTATTATTTAATATCACCCTGTCATTTACTGTCTGATTAATTTTTGTTATAATTTCTATTAAATAA... |
Task1_train_42458 | Chromosome 12 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | AATGTGGGGACAAAGACATTTCTTACAGAACATCTGCAAGGCTTACTGGTTCTGTTTAAGGCAAAATGTGTGAATTTTATCTTTCTAAAATCAGGCAGCAAAGATGTGGCTTAAAGTTCATGTTACTCTCATCTTTGTCCCAACATGAGATCTCATCAAACGTATGCAGCACGTTGGGAGATAGATATTTATAATTTGCAGGAACATTTGGACAGGAAGTGTAACCTCTCAGAGGCTCCCTTGCCACATCAGGAGAATTGGTAAAACCACACTACCTGTATCATATCATTATTTTAAGTGATAAATGATCATCTACATTC... | AATGTGGGGACAAAGACATTTCTTACAGAACATCTGCAAGGCTTACTGGTTCTGTTTAAGGCAAAATGTGTGAATTTTATCTTTCTAAAATCAGGCAGCAAAGATGTGGCTTAAAGTTCATGTTACTCTCATCTTTGTCCCAACATGAGATCTCATCAAACGTATGCAGCACGTTGGGAGATAGATATTTATAATTTGCAGGAACATTTGGACAGGAAGTGTAACCTCTCAGAGGCTCCCTTGCCACATCAGGAGAATTGGTAAAACCACACTACCTGTATCATATCATTATTTTAAGTGATAAATGATCATCTACATTC... |
Task1_train_42459 | An alteration has been detected on Chromosome 12. Is it pathogenic, and if so, what disease is involved? | Benign | TGGTGGAGACCCAAAGGGTTGGAGGCAGCTGGCACAAGAGGCTGAGGCCTGGCTGAATTACCCATGCTTTAAGAATTGGGATGGGTCCCCAGTGAGCTCCTGGATTCTGCTGGTGAGACCTCCTGCTTCCTCCCTGCCATTCATCCCTGCCCCTCTCCATGAAGCTTGAGACATATAGCTGGAGACCATTCTTTCCAAAGAACTTACCTCTTGCCAAAGGCCATTTATATTCATATAGTGACAGGCTGTGCTCCATATTTTACAGTCATTTTGGTCACAATCGAGGGTTTCTGGAATTTTCACATCCCTTGTCCAGAATT... | TGGTGGAGACCCAAAGGGTTGGAGGCAGCTGGCACAAGAGGCTGAGGCCTGGCTGAATTACCCATGCTTTAAGAATTGGGATGGGTCCCCAGTGAGCTCCTGGATTCTGCTGGTGAGACCTCCTGCTTCCTCCCTGCCATTCATCCCTGCCCCTCTCCATGAAGCTTGAGACATATAGCTGGAGACCATTCTTTCCAAAGAACTTACCTCTTGCCAAAGGCCATTTATATTCATATAGTGACAGGCTGTGCTCCATATTTTACAGTCATTTTGGTCACAATCGAGGGTTTCTGGAATTTTCACATCCCTTGTCCAGAATT... |
Task1_train_42460 | Located on Chromosome 12, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | GCATCATCAGTAAGAGGGGGTCATGATGCCTGCCTCTAAAGTAGTCAGAAGGTGTGGACAGCACAAGGAAAGATCCTCTCCTGTCTCTGCCACGGTCCCCAGTGGATACCCCAGCAACAATTTTCCACAGCTCCAGGCTTGTGGGTTAGACAGGAGAAGGTTCTGGAGAGAAAGGAGGAGCCCACGGAGGGGTGGAATGACCCCCAGCCACTGCTCTGCTTCCTCCCAATCTCATTGAGCTCTCCACGATCTCCCTTGCAGGCAGGCCCACTCAGAGACCGCCAACACCACAATAATAAAAATCGCTAATGTTGGGGACC... | GCATCATCAGTAAGAGGGGGTCATGATGCCTGCCTCTAAAGTAGTCAGAAGGTGTGGACAGCACAAGGAAAGATCCTCTCCTGTCTCTGCCACGGTCCCCAGTGGATACCCCAGCAACAATTTTCCACAGCTCCAGGCTTGTGGGTTAGACAGGAGAAGGTTCTGGAGAGAAAGGAGGAGCCCACGGAGGGGTGGAATGACCCCCAGCCACTGCTCTGCTTCCTCCCAATCTCATTGAGCTCTCCACGATCTCCCTTGCAGGCAGGCCCACTCAGAGACCGCCAACACCACAATAATAAAAATCGCTAATGTTGGGGACC... |
Task1_train_42461 | The following genetic variant occurs on Chromosome 12. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TTCGAGACCAGCCCGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAACTTAGCCGGGTGTGGTGGCAGACCCCTGTAATCCCAGTTACTCAGGAGGCCAAGGCAGGAGAATTGCTTGAGCCCGGGAGGCAAAGGTTGCAGTGAGTTGAGATTGTGCCATTGCACTCCAGCCTGGGCGACAGAGCAAGACTCCGTCTCAAAAATAAATAAATTAATTAATTAAAAAAATTTTAAAGGCAAGATACAGAGCAGAGTGTAAAAGGCTGCAATTTGTATAAGCACAGAAAAACACAGTATTAAGAGCGCAGACTCG... | TTCGAGACCAGCCCGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAACTTAGCCGGGTGTGGTGGCAGACCCCTGTAATCCCAGTTACTCAGGAGGCCAAGGCAGGAGAATTGCTTGAGCCCGGGAGGCAAAGGTTGCAGTGAGTTGAGATTGTGCCATTGCACTCCAGCCTGGGCGACAGAGCAAGACTCCGTCTCAAAAATAAATAAATTAATTAATTAAAAAAATTTTAAAGGCAAGATACAGAGCAGAGTGTAAAAGGCTGCAATTTGTATAAGCACAGAAAAACACAGTATTAAGAGCGCAGACTCG... |
Task1_train_42462 | This alteration on Chromosome 12 may affect genome function. Does it lead to a disease or is it benign? | Benign | ACTGTGGGTGTGGGGGTTGGGTGGGGGGGATCATGGAGGGACCCAGGGTTTTGGCAGCATACCCCAACACACCCAGCTCTGGGGCTCTGCAGTAGCCCCTGCACCTGTGCCTCAGCGTTACCCTAATCTGACCACAACTGCTCTGCCTACCTGTGCACCCACACTCCCCACCCTGGCTCTCACCTTGGCCACGGTCTCGCTTCCCACCTCTTCGCTCTGGGCCTCGCCGGTCAGATGCCCCTTCTTCGTCCGAGTCACGATCATCAATTTTCTGTTTCTGTTTCCACTTCTGATAGCTGGGAAACCTCGTTAAGGAAGCT... | ACTGTGGGTGTGGGGGTTGGGTGGGGGGGATCATGGAGGGACCCAGGGTTTTGGCAGCATACCCCAACACACCCAGCTCTGGGGCTCTGCAGTAGCCCCTGCACCTGTGCCTCAGCGTTACCCTAATCTGACCACAACTGCTCTGCCTACCTGTGCACCCACACTCCCCACCCTGGCTCTCACCTTGGCCACGGTCTCGCTTCCCACCTCTTCGCTCTGGGCCTCGCCGGTCAGATGCCCCTTCTTCGTCCGAGTCACGATCATCAATTTTCTGTTTCTGTTTCCACTTCTGATAGCTGGGAAACCTCGTTAAGGAAGCT... |
Task1_train_42463 | Mutation context: Chromosome 12. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TCTCTACATTTGTTGAGCACCTACTGTGTGCCAGGTACTGGCTAGGCTGGAAGATGAGAGAGGGACAGTGGGATGAGGTCTCTTCTAGTTCCTGCCTTGGAGTGTGATCCTTTCTCTTCATATAAATGTCCACTTACTCATCTTGCCCTGAGCCTACCTGGTGCCAGGCACCCGCTGGGAACAGGACTGTGGGAAATAATGGGCGCAGCCCTTCTGCCCCATTGGTGCTCACACCCATCCCTTCATGTGCATACACATGACATTCAGTAATGGAAACGGCACAGGCCTTGGAATCAGACAGTCTCAAGTTTGAATCTCCT... | TCTCTACATTTGTTGAGCACCTACTGTGTGCCAGGTACTGGCTAGGCTGGAAGATGAGAGAGGGACAGTGGGATGAGGTCTCTTCTAGTTCCTGCCTTGGAGTGTGATCCTTTCTCTTCATATAAATGTCCACTTACTCATCTTGCCCTGAGCCTACCTGGTGCCAGGCACCCGCTGGGAACAGGACTGTGGGAAATAATGGGCGCAGCCCTTCTGCCCCATTGGTGCTCACACCCATCCCTTCATGTGCATACACATGACATTCAGTAATGGAAACGGCACAGGCCTTGGAATCAGACAGTCTCAAGTTTGAATCTCCT... |
Task1_train_42464 | Consider a variant on Chromosome 12. Determine its clinical classification and disease relevance. | Benign | GGCAAAAGCTTGCCCTTTCAAAGACTTGCAGTTTGGGGATAGAAGCACTTTCAGTCCTGGCCAAAAAAACTATGGGCGTGGAATCTTGCAGGTATGCCGTGAATATCTGTTGAATAAAAAAAAAAAAAAAAAAAAAGGCCAGACAGGCTGACTCAGGCCTGTAGTCCCAGCACTTTGGGAGGCTGAGGTGGGAGGATCGCTTGAGCTCCAGAGTTTGAGACCAGCCTGGGCAACATAGTGAGATCCCTGTCTCTACAAAAAATAAAAATATTAGCAGGGCATAGTGGTGCATACCTGTAGTCCCAGCTACTCTGGAGGCT... | GGCAAAAGCTTGCCCTTTCAAAGACTTGCAGTTTGGGGATAGAAGCACTTTCAGTCCTGGCCAAAAAAACTATGGGCGTGGAATCTTGCAGGTATGCCGTGAATATCTGTTGAATAAAAAAAAAAAAAAAAAAAAAGGCCAGACAGGCTGACTCAGGCCTGTAGTCCCAGCACTTTGGGAGGCTGAGGTGGGAGGATCGCTTGAGCTCCAGAGTTTGAGACCAGCCTGGGCAACATAGTGAGATCCCTGTCTCTACAAAAAATAAAAATATTAGCAGGGCATAGTGGTGCATACCTGTAGTCCCAGCTACTCTGGAGGCT... |
Task1_train_42465 | A mutation has occurred on Chromosome 12. What is the medical relevance of this mutation? | Benign | GCATGCATGCATCTGTATATATGTTGCATGTGTGTGCATGTACTCCTATGTGTGTTGTGTGTGTTGTATATGTGTGCATGTATTTGTGTGTGTGCATATATTTGTATGTGTGTTGTGTGTATACACGTATGTGTATGTGTTGTATGTGTGCATGTATTTGTGTGCATGTACATGTGTGAGTTGTGTGTGTGCATGTATGTGTATGTGTGCATGTATTTGTATATGTGTGAGTTGTGTATTTGTGTATGTGTGTTGTGTGCATGTATTTGTGTATATGACTGTATTTGAATATTATTGATTTCTTTGTATTTATTTTTTAT... | GCATGCATGCATCTGTATATATGTTGCATGTGTGTGCATGTACTCCTATGTGTGTTGTGTGTGTTGTATATGTGTGCATGTATTTGTGTGTGTGCATATATTTGTATGTGTGTTGTGTGTATACACGTATGTGTATGTGTTGTATGTGTGCATGTATTTGTGTGCATGTACATGTGTGAGTTGTGTGTGTGCATGTATGTGTATGTGTGCATGTATTTGTATATGTGTGAGTTGTGTATTTGTGTATGTGTGTTGTGTGCATGTATTTGTGTATATGACTGTATTTGAATATTATTGATTTCTTTGTATTTATTTTTTAT... |
Task1_train_42466 | This mutation occurs on Chromosome 12. Does this change lead to a known medical condition, or is it benign? | Benign | CTGCAGCCTCCGCCTCCTGAGCTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGCCAGCCACCATCCTTGGCTAATTTTTCTATTTTCAGTAGAGACAGGGTTTCACCATGTTGGCCAGTCTAATCTCAAACTCCTGACCTCAAGTGATCCGCCTGCCTTGGCTTCCCAAAGTGCTGGGATTATAGGCATAAGTCACCACACCCGGACTGAAGGCAGGATTTGATGCCATGCCTTTTGGGCCCCAGAGCCCAAGCTTGGCCACCCCACCAAGCCACCCCCCAGCACAAATGGAAGACATTATT... | CTGCAGCCTCCGCCTCCTGAGCTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGCCAGCCACCATCCTTGGCTAATTTTTCTATTTTCAGTAGAGACAGGGTTTCACCATGTTGGCCAGTCTAATCTCAAACTCCTGACCTCAAGTGATCCGCCTGCCTTGGCTTCCCAAAGTGCTGGGATTATAGGCATAAGTCACCACACCCGGACTGAAGGCAGGATTTGATGCCATGCCTTTTGGGCCCCAGAGCCCAAGCTTGGCCACCCCACCAAGCCACCCCCCAGCACAAATGGAAGACATTATT... |
Task1_train_42467 | This genomic variant is located on Chromosome 12. Can you determine its pathogenicity and name any linked disease? | Benign | GAGCCCGGGACTTCAAGGTTACAGTGAGCCATGATCGTGCCACTGCACTCCAGCCCAGGCAACAGAGTGAGACCTTGTCTCTAAAACAAACACCAAAAAAACAAGAAAGCGGAAGGATTATGGAGTAGGGGGAGTTCATCCTGACAATCCCAGGATCCCCAGGGGAAAAATCTGGGGATTTCACCAAAAAGGAAGAGAGACCCAATTCCAAGTGGACAGACACCCAACATGGGTGCCCTTACCATGCAGGCTCATTGAATCCTCACAATAGTCCTGCCATGTACACGCTCTTCTTGCAGTTTGTTGTGTGGTTGGTTGGT... | GAGCCCGGGACTTCAAGGTTACAGTGAGCCATGATCGTGCCACTGCACTCCAGCCCAGGCAACAGAGTGAGACCTTGTCTCTAAAACAAACACCAAAAAAACAAGAAAGCGGAAGGATTATGGAGTAGGGGGAGTTCATCCTGACAATCCCAGGATCCCCAGGGGAAAAATCTGGGGATTTCACCAAAAAGGAAGAGAGACCCAATTCCAAGTGGACAGACACCCAACATGGGTGCCCTTACCATGCAGGCTCATTGAATCCTCACAATAGTCCTGCCATGTACACGCTCTTCTTGCAGTTTGTTGTGTGGTTGGTTGGT... |
Task1_train_42468 | Here’s a variant located on Chromosome 12. What is the predicted biological effect — harmless or disease-causing? | Benign | AGGATAACAAATCGTAAAGAAATAAGTTACAACGTGGCAAGAAGGCACGGTGACAGAAGAGGAGAGTAGAGGATGGAGAAATTACTGATACCTGTGGAGGGGGAGGGAAAGCGAAGGCTTCCTGGAGGAGGTGTCATTCTATCTGGGTTTTGAAGGCATTTATCAGGTTAAAAAAAAAAAGTGAGGGGCAAGGCATTCTAAGCAGAGGGAACAGCATGTGCAAAGGCACAGAATCCTGTCTGGAGTCTGGGGAACAATGAACTCTGTGGGAGGTGTGGTGGGAGGAAGGAGGAGTCTGGGAAGACCACAGTGTGGGCAGG... | AGGATAACAAATCGTAAAGAAATAAGTTACAACGTGGCAAGAAGGCACGGTGACAGAAGAGGAGAGTAGAGGATGGAGAAATTACTGATACCTGTGGAGGGGGAGGGAAAGCGAAGGCTTCCTGGAGGAGGTGTCATTCTATCTGGGTTTTGAAGGCATTTATCAGGTTAAAAAAAAAAAGTGAGGGGCAAGGCATTCTAAGCAGAGGGAACAGCATGTGCAAAGGCACAGAATCCTGTCTGGAGTCTGGGGAACAATGAACTCTGTGGGAGGTGTGGTGGGAGGAAGGAGGAGTCTGGGAAGACCACAGTGTGGGCAGG... |
Task1_train_42469 | This variant is present on Chromosome 12. Is the change likely to result in a pathogenic outcome? | Benign | TTGGTGTGCAGACAGCAGGCTGCATCACTACTTAGCTGTGTGATCGTGGGTCAGGGCACCTCTCTGGGCATCAGTTTCCATATGTGCAAAATGAAGACAGCAGTCTTCTTGTCGGTGAAACAGACACTGCCCAAAACAGGAGGCCTCACCTAGTCAGTGTTCTCCAACTGTGGCTCACACAGAGAGAGCTTTTGGTGACTGGCATGTCCTCCCAAAGCAGAAGGAAGAAAGGATGGTGTCACATTCCAAAGGATGCTCACATCTCAGTCATGGGGCCCCACCTAGATAATTTTTCTTATGGGTCAGGCGCAGACTGACTT... | TTGGTGTGCAGACAGCAGGCTGCATCACTACTTAGCTGTGTGATCGTGGGTCAGGGCACCTCTCTGGGCATCAGTTTCCATATGTGCAAAATGAAGACAGCAGTCTTCTTGTCGGTGAAACAGACACTGCCCAAAACAGGAGGCCTCACCTAGTCAGTGTTCTCCAACTGTGGCTCACACAGAGAGAGCTTTTGGTGACTGGCATGTCCTCCCAAAGCAGAAGGAAGAAAGGATGGTGTCACATTCCAAAGGATGCTCACATCTCAGTCATGGGGCCCCACCTAGATAATTTTTCTTATGGGTCAGGCGCAGACTGACTT... |
Task1_train_42470 | This genomic variant is located on Chromosome 12. Can you determine its pathogenicity and name any linked disease? | Benign | CAACCATATACTCTAATTTTCTACAGTGAAGGTTGTCCAAGCCTGGTTTCCCACAGTAAGCAAGCCTGAGCCCTGGGTTTGTAGGCAGCTAGTTTATTTACAGAAGTGATTCTAGAGAAGAGGCCTGAGAGACTAAGAAGAGTTAGACAAGGAATAAGGGACAGTTAATTGCAAGAGCATCTTTGAGCCTGGAGTGGTGGCTCACACCTGTAACCCCAGCACTTTGGGAGGCTGAGGTGGGTGGATCACTTGAGGTCAGGAGTTCAAGACTAGTCTGGCCAACATGGTGAAACCCTATCTCTACTAAAAATACAAAAACT... | CAACCATATACTCTAATTTTCTACAGTGAAGGTTGTCCAAGCCTGGTTTCCCACAGTAAGCAAGCCTGAGCCCTGGGTTTGTAGGCAGCTAGTTTATTTACAGAAGTGATTCTAGAGAAGAGGCCTGAGAGACTAAGAAGAGTTAGACAAGGAATAAGGGACAGTTAATTGCAAGAGCATCTTTGAGCCTGGAGTGGTGGCTCACACCTGTAACCCCAGCACTTTGGGAGGCTGAGGTGGGTGGATCACTTGAGGTCAGGAGTTCAAGACTAGTCTGGCCAACATGGTGAAACCCTATCTCTACTAAAAATACAAAAACT... |
Task1_train_42471 | This variant is found on Chromosome 12. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GGCTAGCTTAGTGGTTAGCTAGTTATCAAATGGAGATTTCCTTAAATCCACTGAACCAGTAAGTCTCCCAGCCTTTGCTGAGGTGCTCTCTGTATATTGGGGTACTGCTTCACCATTCTAGCAGCTTACAGCTCTGCCTTAGCCTTCACTTCCTGCTTGTGCAGAGCCTCAGGGTCAGCCAGAGGGGAGAGGTTAGGGCCTTCTCTGGTCTTTCCTGGGCACACACATAGCCCTATACATTCACGTGGCATTCCAGACTCCCAGGAATATATTGGAGCCTTTCAGAGCCTCCTATGGACATCCCATTTCCAAGCTTTTTC... | GGCTAGCTTAGTGGTTAGCTAGTTATCAAATGGAGATTTCCTTAAATCCACTGAACCAGTAAGTCTCCCAGCCTTTGCTGAGGTGCTCTCTGTATATTGGGGTACTGCTTCACCATTCTAGCAGCTTACAGCTCTGCCTTAGCCTTCACTTCCTGCTTGTGCAGAGCCTCAGGGTCAGCCAGAGGGGAGAGGTTAGGGCCTTCTCTGGTCTTTCCTGGGCACACACATAGCCCTATACATTCACGTGGCATTCCAGACTCCCAGGAATATATTGGAGCCTTTCAGAGCCTCCTATGGACATCCCATTTCCAAGCTTTTTC... |
Task1_train_42472 | Here is a variant on Chromosome 12. Please identify whether it is a benign mutation or associated with a disorder. | Benign | ACTGGTACTAAAAAGGTTTCTGGCCATGCTTAACTCAGGAAACCTGAGACCCATAAAGTTAAAATGATTTAATCAGTAAGAAGTCAGGAACAGAACTAACTACTCCCCTAAACCATGAGACCATGCTCCCTTGTTTCTAAAAAAAAAAAAAATTTTTTTTTGAGACAGAGTTTCACTCTTGTCGCCTGGGCTGGAGTGCAATGGCACGGCCTCGTCTCACTGCAACCTCTGCCTCCTGGGTTCAAGTGATTCTCCTGCTTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGTGCCAACATGCTCAGCTAATTTTGCATT... | ACTGGTACTAAAAAGGTTTCTGGCCATGCTTAACTCAGGAAACCTGAGACCCATAAAGTTAAAATGATTTAATCAGTAAGAAGTCAGGAACAGAACTAACTACTCCCCTAAACCATGAGACCATGCTCCCTTGTTTCTAAAAAAAAAAAAAATTTTTTTTTGAGACAGAGTTTCACTCTTGTCGCCTGGGCTGGAGTGCAATGGCACGGCCTCGTCTCACTGCAACCTCTGCCTCCTGGGTTCAAGTGATTCTCCTGCTTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGTGCCAACATGCTCAGCTAATTTTGCATT... |
Task1_train_42473 | Given this variant on Chromosome 12, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CCTTGGCCTCCCAGAGTGCTGAGATTATAGGCATGAGCCACTGTTGTGCCCGGCCTGGACTGTGCATTTCTTCTTCTTCTTCTTCTTCTTTTTTTTTTTTTTTTTGAGACAGAGTTTCATTCTTGTTGCCCAGGCTGGAGTGCAATGGCACAATCATGGCTCACCGCAACCTCTGCCTCCCAGGTTCAAGCAATTCTCCTGCTTCAACCTCCCAAGCAGCTGGGATTACAGGCATGCGCCACTACATGCGGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCTGCATGTTGGTCAGGCTGGTCTCGAACTCCCGAC... | CCTTGGCCTCCCAGAGTGCTGAGATTATAGGCATGAGCCACTGTTGTGCCCGGCCTGGACTGTGCATTTCTTCTTCTTCTTCTTCTTCTTTTTTTTTTTTTTTTTGAGACAGAGTTTCATTCTTGTTGCCCAGGCTGGAGTGCAATGGCACAATCATGGCTCACCGCAACCTCTGCCTCCCAGGTTCAAGCAATTCTCCTGCTTCAACCTCCCAAGCAGCTGGGATTACAGGCATGCGCCACTACATGCGGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCTGCATGTTGGTCAGGCTGGTCTCGAACTCCCGAC... |
Task1_train_42474 | An alteration has been detected on Chromosome 12. Is it pathogenic, and if so, what disease is involved? | Benign | TGAGTGTGTGTGTGTCTGTGTGTGTGTGCATGTGTATATATATTTATATATATATATCACAATAAGATGACAGAGTGGAACAAAAGTCTCTTATTTTAATCATATGGTGGCCCCTGTTTGGTAAAAATCACATAGCAATTAAAACATCAAGAACAATTCCAAATATGGGGGGAACTGGAGTGGAGGATGAGAAATGACAAAGATAAAAATTCTAGGATGAGAATATAAGGCTGTGCCTTTTACTTTTACAAACAAATAATTATAAAATGATGTCAACTTTTCACCATCTCTTTCTGAGTGTTTATAGAATGGAATTTCTA... | TGAGTGTGTGTGTGTCTGTGTGTGTGTGCATGTGTATATATATTTATATATATATATCACAATAAGATGACAGAGTGGAACAAAAGTCTCTTATTTTAATCATATGGTGGCCCCTGTTTGGTAAAAATCACATAGCAATTAAAACATCAAGAACAATTCCAAATATGGGGGGAACTGGAGTGGAGGATGAGAAATGACAAAGATAAAAATTCTAGGATGAGAATATAAGGCTGTGCCTTTTACTTTTACAAACAAATAATTATAAAATGATGTCAACTTTTCACCATCTCTTTCTGAGTGTTTATAGAATGGAATTTCTA... |
Task1_train_42475 | This variant is found on Chromosome 12. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CCTACACCCCAGGCTGAATTATCTCTCGGCAGCTAAGCCCTACTGGCCTGGGCCAGAGAATCATACAAGGCTTTAGCAACTTACCTGTTAAATAAATGGTTAACATCACAAACACTACCCCGGGCCTCCTCTGCTGTCCCATCTCCTCCTGATGGTGTTGGCATCTGAGCTCCCAGTGCCTACTGAGCTGAGGAGCTTCCTAGCAGAAATGGAAGCAAACTGAGAGCTGGCACGCAGGTTACACATTCAGTAGAAACATGATTTTCAAGCCACAGAGCAGTCAGGGGCACTCCAGGGCATGAATCCCAGGCGCTAGTTCC... | CCTACACCCCAGGCTGAATTATCTCTCGGCAGCTAAGCCCTACTGGCCTGGGCCAGAGAATCATACAAGGCTTTAGCAACTTACCTGTTAAATAAATGGTTAACATCACAAACACTACCCCGGGCCTCCTCTGCTGTCCCATCTCCTCCTGATGGTGTTGGCATCTGAGCTCCCAGTGCCTACTGAGCTGAGGAGCTTCCTAGCAGAAATGGAAGCAAACTGAGAGCTGGCACGCAGGTTACACATTCAGTAGAAACATGATTTTCAAGCCACAGAGCAGTCAGGGGCACTCCAGGGCATGAATCCCAGGCGCTAGTTCC... |
Task1_train_42476 | Located on Chromosome 12, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | CCATGACAGGCATGAGATAGGACAAATACGTCTGTCCAACTCTCAGCTGATGCCATTTCCCACTTGCAAAGAGAGGGCATCTCGGCCACATAGAGAGTGGTTCTAGAATTTAAAGATACAGTTACATATAACTATTTATTTATTTTCATTTTTTTTAGAGACAAGGTCTCACTCTGTCACCCAGACTGAGATGCAGTGGTACAATCACGGCTTACTGCAGCCTCAAACTCCTGGGCTCAAGCAATCCTCCTGCCTCAGCCTCCCGAGTAACTGGGACTCCAGGCACGTGCCACCACGCCAAGCTAATTTTTACTTTTTTA... | CCATGACAGGCATGAGATAGGACAAATACGTCTGTCCAACTCTCAGCTGATGCCATTTCCCACTTGCAAAGAGAGGGCATCTCGGCCACATAGAGAGTGGTTCTAGAATTTAAAGATACAGTTACATATAACTATTTATTTATTTTCATTTTTTTTAGAGACAAGGTCTCACTCTGTCACCCAGACTGAGATGCAGTGGTACAATCACGGCTTACTGCAGCCTCAAACTCCTGGGCTCAAGCAATCCTCCTGCCTCAGCCTCCCGAGTAACTGGGACTCCAGGCACGTGCCACCACGCCAAGCTAATTTTTACTTTTTTA... |
Task1_train_42477 | This mutation is located on Chromosome 12. Is it associated with a disease or is it a benign polymorphism? | Benign | TAATAGCTGCAGTTACAAATACTTTGTAGAATTGCCATAGACTCTTCACCCTTCATCTGTGCTGCCTTACATGGGAACATGTATTGGCCAACCCAGGAGAAAAATGGAATCAAGCAGGCCAGAAGCAGTTCCTTCCTCCACTTCATCTCCCACTCTGCCTCCCACCCAACTCTTCCACAAGCATCATTCAACTTTGAAACAACAATGCTTTTCAACTTTCACTTTACACTTCAAAGCCTCAGAGCAGTAGGCACCATAGCCCAATTTCATTGATGGTGACTGCAGAGAAAACACTTTGCCTCCTCCCACACATCAATATT... | TAATAGCTGCAGTTACAAATACTTTGTAGAATTGCCATAGACTCTTCACCCTTCATCTGTGCTGCCTTACATGGGAACATGTATTGGCCAACCCAGGAGAAAAATGGAATCAAGCAGGCCAGAAGCAGTTCCTTCCTCCACTTCATCTCCCACTCTGCCTCCCACCCAACTCTTCCACAAGCATCATTCAACTTTGAAACAACAATGCTTTTCAACTTTCACTTTACACTTCAAAGCCTCAGAGCAGTAGGCACCATAGCCCAATTTCATTGATGGTGACTGCAGAGAAAACACTTTGCCTCCTCCCACACATCAATATT... |
Task1_train_42478 | A change on Chromosome 12 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GACTCCTAAACCATAATTTCTAATCTTCTGGCTAGTTTTTTAGTCCTACAAAGACAATCTAGTCCCCAGGCAAAAAGGAGGTTTGTTTTGAGAGAGGGCTGTTATCGTCATTGTTTTTTGTTTTTCTGTGTTTGTGTTTGTTTGTTTGTTTGTTTTTTGTTTTGAGACAGAGTCTCGCTCTGTTGCCCAGGCTGGCGTGCAGTGGCACAGTCTCAGCTCACTGCAACCTCCGCCTCCCGGGTTCACGCCATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGAGCCCACCACCACGCCTGGCTAATTTTTTTG... | GACTCCTAAACCATAATTTCTAATCTTCTGGCTAGTTTTTTAGTCCTACAAAGACAATCTAGTCCCCAGGCAAAAAGGAGGTTTGTTTTGAGAGAGGGCTGTTATCGTCATTGTTTTTTGTTTTTCTGTGTTTGTGTTTGTTTGTTTGTTTGTTTTTTGTTTTGAGACAGAGTCTCGCTCTGTTGCCCAGGCTGGCGTGCAGTGGCACAGTCTCAGCTCACTGCAACCTCCGCCTCCCGGGTTCACGCCATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGAGCCCACCACCACGCCTGGCTAATTTTTTTG... |
Task1_train_42479 | With a mutation on Chromosome 12, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CAGGACCCATTTCCAAGACAGCTCACTCACATTGGTGGCAAGTTGTATTTGGCTGTCAGTTCGTGAGCTTGGTTCCTTTCCCTGTGGGCCTCCTCACAGGCTGCCAGCTTCCCCACAGCATGGCAGCTGAATGCTGAGTGAGCATCCCAGGACACAGGAAGGAGAGGTTGCCAGTTCCTGGTGCCCGGAATCACATGACTTCTGACATATTCTGTTAGGTCAGCTGGTCACAGAGCCAAATGAACATAGACCTACCTCTCGATTGGAGAAGTTTCAAAGAATTTGGGGGACATGTTTTGAAATTTCCACAACTTCCTCAA... | CAGGACCCATTTCCAAGACAGCTCACTCACATTGGTGGCAAGTTGTATTTGGCTGTCAGTTCGTGAGCTTGGTTCCTTTCCCTGTGGGCCTCCTCACAGGCTGCCAGCTTCCCCACAGCATGGCAGCTGAATGCTGAGTGAGCATCCCAGGACACAGGAAGGAGAGGTTGCCAGTTCCTGGTGCCCGGAATCACATGACTTCTGACATATTCTGTTAGGTCAGCTGGTCACAGAGCCAAATGAACATAGACCTACCTCTCGATTGGAGAAGTTTCAAAGAATTTGGGGGACATGTTTTGAAATTTCCACAACTTCCTCAA... |
Task1_train_42480 | A variant affecting Chromosome 12 has been observed. Determine if it's benign or associated with disease. | Benign | ATACCTTCCATGTATGGTCGTGTATTTCTTGATGCTGAAGCCAGATCCTACCCCAAAAATGATCTCTGTAGGTCCCTAAAAACAGCTAGGATAGGAGCTGGACTTGAGGGTGGGAGGGAAGGGGTCTGTGGGAAAACAACCAGAACTTACAATGAGGATGGGGGAGTCTAAGGATTCAGAAGGAAGCTGGAATAGGAGACTTAAACAGCAGTCCCTCACATCAACAAATACCCTGAGTGGGGAAGCTGGGAGGATCTACAAAAAGGAACTATTTCTACCATTTCTTTTGAAATGTAAGGGTTTTCATCTTTTACCTCCAA... | ATACCTTCCATGTATGGTCGTGTATTTCTTGATGCTGAAGCCAGATCCTACCCCAAAAATGATCTCTGTAGGTCCCTAAAAACAGCTAGGATAGGAGCTGGACTTGAGGGTGGGAGGGAAGGGGTCTGTGGGAAAACAACCAGAACTTACAATGAGGATGGGGGAGTCTAAGGATTCAGAAGGAAGCTGGAATAGGAGACTTAAACAGCAGTCCCTCACATCAACAAATACCCTGAGTGGGGAAGCTGGGAGGATCTACAAAAAGGAACTATTTCTACCATTTCTTTTGAAATGTAAGGGTTTTCATCTTTTACCTCCAA... |
Task1_train_42481 | A mutation has occurred on Chromosome 12. What is the medical relevance of this mutation? | Benign | ACCTCAGATGCTGGTACTTACTTAACCAAGGGATTTGGCCAGGAAGGGCATCCTCCCCTGCCCCTCCCGCCTGGCACTGCCCCCTGCCAGTGCTGCAGCGTGCCATCCGCAAGGCAGGCCTGCCAACGCTGCTTCCCAGGCCAGCAGGGCCCTAAAGCTTGGCAGAAACTTCAAGCCAGAAAGAAACCACGCCAGGCAAAGGCTTCCACTGCATCCTTCCAGGCATGTGGAGGATAAACACGGAGCTTCCCCTGGCATCTTACCACATGTGCTCCCAGTCCAACTAGGGGGAGACTCAACCCTGGCCCACCTGTTCATGG... | ACCTCAGATGCTGGTACTTACTTAACCAAGGGATTTGGCCAGGAAGGGCATCCTCCCCTGCCCCTCCCGCCTGGCACTGCCCCCTGCCAGTGCTGCAGCGTGCCATCCGCAAGGCAGGCCTGCCAACGCTGCTTCCCAGGCCAGCAGGGCCCTAAAGCTTGGCAGAAACTTCAAGCCAGAAAGAAACCACGCCAGGCAAAGGCTTCCACTGCATCCTTCCAGGCATGTGGAGGATAAACACGGAGCTTCCCCTGGCATCTTACCACATGTGCTCCCAGTCCAACTAGGGGGAGACTCAACCCTGGCCCACCTGTTCATGG... |
Task1_train_42482 | A mutation is present on Chromosome 12. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | AGACTTTTTAAAGAAGTAAGCCTTTATTTCCTTGTTTTGCAAATAAAACTGGCTAAGTTGGTTGCTTTTTGGTGATTAGTCAAAGAGACCAAATCCCATATCCTCGTCCGACTCCTCCGACTCTTCCTTGGCTTCAACCTTAGCTGGGGCTGCAGCAGCAGCAGGAGCAGCTGTGGTGGCAGCAGCCACAGGGGCAGCAGCCACAAAGGCAGATGGATCAGCCAAGAAGGCCTTGACCTGAAAGGAGGGGGGAAGTGGTCAAAATGGTCATCCACACTCCTCTATTACCCACCACCCTCCTGCCTTGGTAGAGTTTAAGG... | AGACTTTTTAAAGAAGTAAGCCTTTATTTCCTTGTTTTGCAAATAAAACTGGCTAAGTTGGTTGCTTTTTGGTGATTAGTCAAAGAGACCAAATCCCATATCCTCGTCCGACTCCTCCGACTCTTCCTTGGCTTCAACCTTAGCTGGGGCTGCAGCAGCAGCAGGAGCAGCTGTGGTGGCAGCAGCCACAGGGGCAGCAGCCACAAAGGCAGATGGATCAGCCAAGAAGGCCTTGACCTGAAAGGAGGGGGGAAGTGGTCAAAATGGTCATCCACACTCCTCTATTACCCACCACCCTCCTGCCTTGGTAGAGTTTAAGG... |
Task1_train_42483 | A variant on Chromosome 12 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | CCGTCTCCACAGACAAGGCCAGGACTCGTTTGTACCCGTTGATGATAGAATGGGGTACTGATGCAACAGTTGGGTAGCCAATCTGCAGACAGACACTGGCAACATTGCGGACACCCTGGGGGAGGGAAGATTTCATTTTACGTGAGATTCCCTACAGGAAAGGAAGTCCAAGTAAGGGTGAATAAAGAGAACCCTTAGCAGACAATAATTGCCAGGTTGGCAGCTCAGTCTCAAGAGAGGCCATTTCATCTCATACCAAATGCTCCTGGCAGAGCAATTCAGCCCCATCAAATAAATTTTGCCCTTATTCCAAATCCAGG... | CCGTCTCCACAGACAAGGCCAGGACTCGTTTGTACCCGTTGATGATAGAATGGGGTACTGATGCAACAGTTGGGTAGCCAATCTGCAGACAGACACTGGCAACATTGCGGACACCCTGGGGGAGGGAAGATTTCATTTTACGTGAGATTCCCTACAGGAAAGGAAGTCCAAGTAAGGGTGAATAAAGAGAACCCTTAGCAGACAATAATTGCCAGGTTGGCAGCTCAGTCTCAAGAGAGGCCATTTCATCTCATACCAAATGCTCCTGGCAGAGCAATTCAGCCCCATCAAATAAATTTTGCCCTTATTCCAAATCCAGG... |
Task1_train_42484 | This sequence variant lies on Chromosome 12. Is it clinically significant, and what condition might it cause if any? | Benign | CCAGAAACCATTCCAAGCGCTTTACATGGATTACTGGTTCTCACCCTTACTGAGGTAGGTGGTCTTATCCCAGTGATCCCATAAGTTCTTGTCCCATTTTACAGATGGGAAAACTAAGGCTTGAGAGCTGACAGTAACTGTCAGAGCCAAGATGTGAACCCCACTGTGTGGCCCCAAAGCCTGTGCTAAGAGCTGCTAAGCTCCAGGCGCCCTCAGCCTGCACAACGTCTGTCCTTTCTGACTGGCAGTGACTGGCTGAAGGCAGGGATGGTGTCCATGTGACTCACCACTATCCCCCCAGTGCCTGGCAAATGGCAGAC... | CCAGAAACCATTCCAAGCGCTTTACATGGATTACTGGTTCTCACCCTTACTGAGGTAGGTGGTCTTATCCCAGTGATCCCATAAGTTCTTGTCCCATTTTACAGATGGGAAAACTAAGGCTTGAGAGCTGACAGTAACTGTCAGAGCCAAGATGTGAACCCCACTGTGTGGCCCCAAAGCCTGTGCTAAGAGCTGCTAAGCTCCAGGCGCCCTCAGCCTGCACAACGTCTGTCCTTTCTGACTGGCAGTGACTGGCTGAAGGCAGGGATGGTGTCCATGTGACTCACCACTATCCCCCCAGTGCCTGGCAAATGGCAGAC... |
Task1_train_42485 | This mutation on Chromosome 12 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | AGGCTGAGGCACAAGAATTGCTTGAACCCGGGAGGCAGAGGTTGTAGTGACCCGAGATCGCTCCACTGTACTCCATCCTGGGCAACAGGGCAAGACTCTGTCTCAGAAACAACAACAACAACAACAACAACAACAACAACAACAAAAACTGGGCCAACAGGGTGCAGTTGCCAGGACGGAGTTTCTCTCTTGTTGCCTAGGCTGGAGTGCAATGGCACCATCTTGGTTCACCACAACCTCCACCTTCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTTCAAATAGCTGGGATTACAGGCATGTGTCACCACACCCAGCTA... | AGGCTGAGGCACAAGAATTGCTTGAACCCGGGAGGCAGAGGTTGTAGTGACCCGAGATCGCTCCACTGTACTCCATCCTGGGCAACAGGGCAAGACTCTGTCTCAGAAACAACAACAACAACAACAACAACAACAACAACAACAAAAACTGGGCCAACAGGGTGCAGTTGCCAGGACGGAGTTTCTCTCTTGTTGCCTAGGCTGGAGTGCAATGGCACCATCTTGGTTCACCACAACCTCCACCTTCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTTCAAATAGCTGGGATTACAGGCATGTGTCACCACACCCAGCTA... |
Task1_train_42486 | Mutation context: Chromosome 12. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | ATTGTGAGCTTTTTGTTTTTTTAAGTTCATTACAGGTAAGCTAGACAAGTTATTTCTTGAATAGGTTAACGTGACAGCTACTATGATATTGTAGGCTGTCTTTTCTGGTGTCAGGTTTAAATGGTTCTAGAGCTGGGCTTAGCTTTAACCTGCCATTTTAAAAGAAATCCTATCAGGAAATTTCCTGGATGGATGAGGGTGTTCTGGCCTCCAGATGAGGGGGCATGTTGAAGCCAGAATCACCAGTGTTTCTGTTAAATGTGTATGGTACTTTCAGTCTCATCCATTGTATTATGGAGAAAACAGATCCCAGAAATGTC... | ATTGTGAGCTTTTTGTTTTTTTAAGTTCATTACAGGTAAGCTAGACAAGTTATTTCTTGAATAGGTTAACGTGACAGCTACTATGATATTGTAGGCTGTCTTTTCTGGTGTCAGGTTTAAATGGTTCTAGAGCTGGGCTTAGCTTTAACCTGCCATTTTAAAAGAAATCCTATCAGGAAATTTCCTGGATGGATGAGGGTGTTCTGGCCTCCAGATGAGGGGGCATGTTGAAGCCAGAATCACCAGTGTTTCTGTTAAATGTGTATGGTACTTTCAGTCTCATCCATTGTATTATGGAGAAAACAGATCCCAGAAATGTC... |
Task1_train_42487 | A variant found on Chromosome 12 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | AATAATACTATTATTATTATTTTGTTTTTGGTAGAGATGGGGTCTTGCTATGTTGCCCAGACTGGTCTCGAACTCCTGGCCTCAAGCAATCCCCTCACCTTGGTCTCCCAAAGTGCTGGGATTACAGGTGTGATCACTGCTCCTGGCCCACTCTTAATATGATTATTACCCAGAATTAAGAGTCCCAAGCTCTTATCCTTCATTCATTCTCTCACTGGCCTTGGGCATGTAGCAGTGAGCAAGAGCACACACAGTCTGTGCCCTCGTGGTGAAGGCAAAAGACCTTAATCCAGAGAAGCACGTTCATCCCTGAGAAATTC... | AATAATACTATTATTATTATTTTGTTTTTGGTAGAGATGGGGTCTTGCTATGTTGCCCAGACTGGTCTCGAACTCCTGGCCTCAAGCAATCCCCTCACCTTGGTCTCCCAAAGTGCTGGGATTACAGGTGTGATCACTGCTCCTGGCCCACTCTTAATATGATTATTACCCAGAATTAAGAGTCCCAAGCTCTTATCCTTCATTCATTCTCTCACTGGCCTTGGGCATGTAGCAGTGAGCAAGAGCACACACAGTCTGTGCCCTCGTGGTGAAGGCAAAAGACCTTAATCCAGAGAAGCACGTTCATCCCTGAGAAATTC... |
Task1_train_42488 | A mutation on Chromosome 12 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TTGGTCTCCCAAAGTGCTGGGATTACAGGTGTGATCACTGCTCCTGGCCCACTCTTAATATGATTATTACCCAGAATTAAGAGTCCCAAGCTCTTATCCTTCATTCATTCTCTCACTGGCCTTGGGCATGTAGCAGTGAGCAAGAGCACACACAGTCTGTGCCCTCGTGGTGAAGGCAAAAGACCTTAATCCAGAGAAGCACGTTCATCCCTGAGAAATTCCAGCCGCAGAAGTGCTGCAGGAGAGGGACTGAAGGATTTGACTCAGCGAGGCTGGGGATGGCAGCCCAAAGCAGCGAGGCCTGAGCTGCGATCAGAAGG... | TTGGTCTCCCAAAGTGCTGGGATTACAGGTGTGATCACTGCTCCTGGCCCACTCTTAATATGATTATTACCCAGAATTAAGAGTCCCAAGCTCTTATCCTTCATTCATTCTCTCACTGGCCTTGGGCATGTAGCAGTGAGCAAGAGCACACACAGTCTGTGCCCTCGTGGTGAAGGCAAAAGACCTTAATCCAGAGAAGCACGTTCATCCCTGAGAAATTCCAGCCGCAGAAGTGCTGCAGGAGAGGGACTGAAGGATTTGACTCAGCGAGGCTGGGGATGGCAGCCCAAAGCAGCGAGGCCTGAGCTGCGATCAGAAGG... |
Task1_train_42489 | Given a variant located on Chromosome 12, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CAGTCTACTCCATTCACTCCACTCCAACCCACTCACTCCACTCCATACCATTCCACTCCACTGTGTTCACACAACTCCATCCATTCCACTCTAGCCACTCCATTCATTCCACTCCACGCCACACTATTCCTCACCATTCCATCCACTCCACCCTATACCATTCCACTCCACTCTATTCCTCCCCACCCGTCCTCTCCACCCTTTACCACTCCACTCGACTGTACCCATTCCACTTGATCCCACTCATTCCACTCAATTCCATCTACTCTACTCCACACCATCCACTCCACTTCATATCATTCCACTCAACTCAACCTAAG... | CAGTCTACTCCATTCACTCCACTCCAACCCACTCACTCCACTCCATACCATTCCACTCCACTGTGTTCACACAACTCCATCCATTCCACTCTAGCCACTCCATTCATTCCACTCCACGCCACACTATTCCTCACCATTCCATCCACTCCACCCTATACCATTCCACTCCACTCTATTCCTCCCCACCCGTCCTCTCCACCCTTTACCACTCCACTCGACTGTACCCATTCCACTTGATCCCACTCATTCCACTCAATTCCATCTACTCTACTCCACACCATCCACTCCACTTCATATCATTCCACTCAACTCAACCTAAG... |
Task1_train_42490 | A mutation on Chromosome 12 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CATTCCACTCCACTGTGTTCACACAACTCCATCCATTCCACTCTAGCCACTCCATTCATTCCACTCCACGCCACACTATTCCTCACCATTCCATCCACTCCACCCTATACCATTCCACTCCACTCTATTCCTCCCCACCCGTCCTCTCCACCCTTTACCACTCCACTCGACTGTACCCATTCCACTTGATCCCACTCATTCCACTCAATTCCATCTACTCTACTCCACACCATCCACTCCACTTCATATCATTCCACTCAACTCAACCTAAGTTGATTTGGGTTAATTCAATTCAATTCATTCATTTCAGATTGTATCAA... | CATTCCACTCCACTGTGTTCACACAACTCCATCCATTCCACTCTAGCCACTCCATTCATTCCACTCCACGCCACACTATTCCTCACCATTCCATCCACTCCACCCTATACCATTCCACTCCACTCTATTCCTCCCCACCCGTCCTCTCCACCCTTTACCACTCCACTCGACTGTACCCATTCCACTTGATCCCACTCATTCCACTCAATTCCATCTACTCTACTCCACACCATCCACTCCACTTCATATCATTCCACTCAACTCAACCTAAGTTGATTTGGGTTAATTCAATTCAATTCATTCATTTCAGATTGTATCAA... |
Task1_train_42491 | A mutation on Chromosome 12 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CAAACCACGGGCTCTGGGAAGGAGAGGTGGTGCCCTTGGGAGGTCTTGGGCAGGGGTGGGATATAACTGGGGGGCCCAGCTGATTCCCTCCCCTTCCACTCCAGGCCTGGCCTCCACGCAGGCACAGAGTGTGCCGGTCATCAACAGCATGGGCAGCAGCCTGACCACCCTGCAGCCCGTCCAGTTCTCCCAGCCGCTGCACCCCTCCTACCAGCAGCCGCTCATGCCACCTGTGCAGAGCCATGTGACCCAGAGCCCCTTCATGGCCACCATGGCTCAGCTGCAGAGCCCCCACGGTGAGCGCCCTGTGCCCCACACAG... | CAAACCACGGGCTCTGGGAAGGAGAGGTGGTGCCCTTGGGAGGTCTTGGGCAGGGGTGGGATATAACTGGGGGGCCCAGCTGATTCCCTCCCCTTCCACTCCAGGCCTGGCCTCCACGCAGGCACAGAGTGTGCCGGTCATCAACAGCATGGGCAGCAGCCTGACCACCCTGCAGCCCGTCCAGTTCTCCCAGCCGCTGCACCCCTCCTACCAGCAGCCGCTCATGCCACCTGTGCAGAGCCATGTGACCCAGAGCCCCTTCATGGCCACCATGGCTCAGCTGCAGAGCCCCCACGGTGAGCGCCCTGTGCCCCACACAG... |
Task1_train_42492 | A variant was discovered on Chromosome 12. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | ATCCAACAATTTATTTATCCATTCGTTGTTTGAGTACATGTAGGTTATTTCCTGCTTTCCCTCTTACAAGCAATGCTGCAGAAACATTCTTGTCCATAGCTCCTCCGGCACATGTACAAGAGCTTCTCTAGGGCACAAATGTAAGAGTTTTATTGCTGGGCCATGGGGAATGCTCTTCTTCAAATGTACTTGCTATTGTCAAATCTGAGCTATCTTTTCAGGAGCCTACTACTGGTTCTCAGCCCTGGCTATGCATTAGAATCACTTGGGAACTTTAAAAAAATATGTGGGTATCTGGATAACTCCCCCGACCCGTGGAA... | ATCCAACAATTTATTTATCCATTCGTTGTTTGAGTACATGTAGGTTATTTCCTGCTTTCCCTCTTACAAGCAATGCTGCAGAAACATTCTTGTCCATAGCTCCTCCGGCACATGTACAAGAGCTTCTCTAGGGCACAAATGTAAGAGTTTTATTGCTGGGCCATGGGGAATGCTCTTCTTCAAATGTACTTGCTATTGTCAAATCTGAGCTATCTTTTCAGGAGCCTACTACTGGTTCTCAGCCCTGGCTATGCATTAGAATCACTTGGGAACTTTAAAAAAATATGTGGGTATCTGGATAACTCCCCCGACCCGTGGAA... |
Task1_train_42493 | This variant lies on Chromosome 12. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CTCCCAAAGTGCTGGGATTACAGGCGTGATAAGCCACGGCGCCCAGCCCCCAGAACATTTTCATCACCTACAAAGGAAACCCCAAATCCAGTAGCAGTCACTCCCCATTCTCCCCTTCCCCTGTCCCTGGCCACAGTCTACTTTCTGTCTCTATAGATGCCTATTCTGGACATTTCCTATAAATAGAATTGTATATGGTGTGGCCTTTTGTGTCTGTCTTCTTTCACTCAGCATCATGTTCTCCAGGTCCATCCATGTTGTAGCCTGTGTCATTGCTTCATCCTTCTTATGGCTAAATAAGATTCTGTGTATGAATGTAC... | CTCCCAAAGTGCTGGGATTACAGGCGTGATAAGCCACGGCGCCCAGCCCCCAGAACATTTTCATCACCTACAAAGGAAACCCCAAATCCAGTAGCAGTCACTCCCCATTCTCCCCTTCCCCTGTCCCTGGCCACAGTCTACTTTCTGTCTCTATAGATGCCTATTCTGGACATTTCCTATAAATAGAATTGTATATGGTGTGGCCTTTTGTGTCTGTCTTCTTTCACTCAGCATCATGTTCTCCAGGTCCATCCATGTTGTAGCCTGTGTCATTGCTTCATCCTTCTTATGGCTAAATAAGATTCTGTGTATGAATGTAC... |
Task1_train_42494 | Here is a mutation located on Chromosome 12. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AGAAGCCTGAAACAACAAACGCCTATTGTCTCCCACGGTTTCTGTGGGTCAGGAATCTGGGAATGACTTTGCTGCGTGGTTCTGGCTCAAGGTCTGTCAGGTTGTAGCCAAGCTGTCAACCAGGGCTGCAGTCATTTCTAGGCTTGACTGGGGCTGGAGAACACTTTTCCAAGCTCTCACACAGTTGCTCGTGGGAGAGCTCAGTTCCTCACCACGTGAACCTCGCCCTAGACCACTTGAGTATCCTTGGTATATGGTGGCTGGCTTCTCCCAGAGCAAGTGACCCAAGAGAGACAGAGCAAGCAACCAAGAGTATAACC... | AGAAGCCTGAAACAACAAACGCCTATTGTCTCCCACGGTTTCTGTGGGTCAGGAATCTGGGAATGACTTTGCTGCGTGGTTCTGGCTCAAGGTCTGTCAGGTTGTAGCCAAGCTGTCAACCAGGGCTGCAGTCATTTCTAGGCTTGACTGGGGCTGGAGAACACTTTTCCAAGCTCTCACACAGTTGCTCGTGGGAGAGCTCAGTTCCTCACCACGTGAACCTCGCCCTAGACCACTTGAGTATCCTTGGTATATGGTGGCTGGCTTCTCCCAGAGCAAGTGACCCAAGAGAGACAGAGCAAGCAACCAAGAGTATAACC... |
Task1_train_42495 | This sequence change occurs on Chromosome 12. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | AGTGAGTGGTAATCCTGCTACTGCACTCCAGCCTGGGTGACAGCGTGAGACCCTGTCTCAAAAAAAAAAAAAAAAAAACCCAAAACCCAGCACTTTCAAAGGGATCTTACAAATACAGATCCTTTTCTTCCTACAGATACGCCAAGTACTACAAGGAAAACAATGTTGAGAAACGGACTCTGATAAAAGTCTTCGGGATCCGTTTTGACATCCTGGTTTTTGGCACCGTAAGTCTCGTTTCCCAGCTCCGGGCACCGGCATCCTATGACTGTGTCCTAATTACTGCTGTGGGGCCTCCATGGAGGGAAGGGTTTTGGTCT... | AGTGAGTGGTAATCCTGCTACTGCACTCCAGCCTGGGTGACAGCGTGAGACCCTGTCTCAAAAAAAAAAAAAAAAAAACCCAAAACCCAGCACTTTCAAAGGGATCTTACAAATACAGATCCTTTTCTTCCTACAGATACGCCAAGTACTACAAGGAAAACAATGTTGAGAAACGGACTCTGATAAAAGTCTTCGGGATCCGTTTTGACATCCTGGTTTTTGGCACCGTAAGTCTCGTTTCCCAGCTCCGGGCACCGGCATCCTATGACTGTGTCCTAATTACTGCTGTGGGGCCTCCATGGAGGGAAGGGTTTTGGTCT... |
Task1_train_42496 | Given this variant on Chromosome 12, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TCATGCATCACTTAATGATGGGGATATGTTCTGAAAAACGCATCAGTAGCTGATTCTGTGGTTGTCTGAATATCATGGACTCTATTTACACAAACCTAAATAGAATAGCCTATTATACTTAGGTTATATGGTGTAGTCTATTGCTCCTAGGCTGCAAACCTGTACAGCATGTTACTGTACTGAATACGGTAAGCAACTGTAACAGAATGGTAAGATTTGTATATCTAAATATAGAAAAGGTACAGTGAAAATATGATATAAAAGCTTAAAAATGGTACATCTGCATAGGGCACTTACCATGAATGGAGCTTGTAGGACTG... | TCATGCATCACTTAATGATGGGGATATGTTCTGAAAAACGCATCAGTAGCTGATTCTGTGGTTGTCTGAATATCATGGACTCTATTTACACAAACCTAAATAGAATAGCCTATTATACTTAGGTTATATGGTGTAGTCTATTGCTCCTAGGCTGCAAACCTGTACAGCATGTTACTGTACTGAATACGGTAAGCAACTGTAACAGAATGGTAAGATTTGTATATCTAAATATAGAAAAGGTACAGTGAAAATATGATATAAAAGCTTAAAAATGGTACATCTGCATAGGGCACTTACCATGAATGGAGCTTGTAGGACTG... |
Task1_train_42497 | A variant was discovered on Chromosome 12. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CCTATTATACTTAGGTTATATGGTGTAGTCTATTGCTCCTAGGCTGCAAACCTGTACAGCATGTTACTGTACTGAATACGGTAAGCAACTGTAACAGAATGGTAAGATTTGTATATCTAAATATAGAAAAGGTACAGTGAAAATATGATATAAAAGCTTAAAAATGGTACATCTGCATAGGGCACTTACCATGAATGGAGCTTGTAGGACTGAAAGTTGCTCTGGGTGAGTCAGTGAGTAGTGAGTGAATGTGAAAGCCTAGGTTGTTACCGTGCACTACAGTAGACTTCATAAACACTGTACACTTAGGCTACACTAAA... | CCTATTATACTTAGGTTATATGGTGTAGTCTATTGCTCCTAGGCTGCAAACCTGTACAGCATGTTACTGTACTGAATACGGTAAGCAACTGTAACAGAATGGTAAGATTTGTATATCTAAATATAGAAAAGGTACAGTGAAAATATGATATAAAAGCTTAAAAATGGTACATCTGCATAGGGCACTTACCATGAATGGAGCTTGTAGGACTGAAAGTTGCTCTGGGTGAGTCAGTGAGTAGTGAGTGAATGTGAAAGCCTAGGTTGTTACCGTGCACTACAGTAGACTTCATAAACACTGTACACTTAGGCTACACTAAA... |
Task1_train_42498 | Mutation context: Chromosome 12. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TCTTGAGGGAGTGGGGACTTTGAAGACCTGAGAGAAGTCCAGGCACAGTGGCCCATGCCTGTAATCCCAGCACTTTGGGAGACCGAGGTGGGTGGATCATCTGAGGTCAGGAGTTTGAGACCAGCCTGACCAACATGGTGAAACCCCATCTCTACTAAAAATATGAAAAAATTAGCCAGGCGTGGTGGTGCACGCCTGTAACCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGAGGTTGCAGTGAGCCGAGATCGCGGCATTGCACTCCAGCCTGAGCAACAGGAGCAAGACTCCATCTCAAAAAA... | TCTTGAGGGAGTGGGGACTTTGAAGACCTGAGAGAAGTCCAGGCACAGTGGCCCATGCCTGTAATCCCAGCACTTTGGGAGACCGAGGTGGGTGGATCATCTGAGGTCAGGAGTTTGAGACCAGCCTGACCAACATGGTGAAACCCCATCTCTACTAAAAATATGAAAAAATTAGCCAGGCGTGGTGGTGCACGCCTGTAACCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGAGGTTGCAGTGAGCCGAGATCGCGGCATTGCACTCCAGCCTGAGCAACAGGAGCAAGACTCCATCTCAAAAAA... |
Task1_train_42499 | A genomic change on Chromosome 12 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CCAGATGGACTGAGGGATGGGTAAGGAATGAACAGACAAGCACAGGAAAAGGTTAATATAGTAGAATCCAGGTGGTGGGTATGTGGGTGTTCACTGGACACTTCTTCCAGCTTTGCTACATGATTGAAAAATTTTCTAATCAAATATTGAGAGGCAATCGGTATAAACTCCTTTACTTCTTCATGGGACCAGTTTCTTAGGCTTTCCTCAATAAGAACACAAGCTCAGGAAAGGGAAAAATCTACGTTTTTATTGCTCACATAATCAAACTGAACTTCAGAGTTAAAACGAGAAGGCCAGGCGTGGTGGCTCACACCTGT... | CCAGATGGACTGAGGGATGGGTAAGGAATGAACAGACAAGCACAGGAAAAGGTTAATATAGTAGAATCCAGGTGGTGGGTATGTGGGTGTTCACTGGACACTTCTTCCAGCTTTGCTACATGATTGAAAAATTTTCTAATCAAATATTGAGAGGCAATCGGTATAAACTCCTTTACTTCTTCATGGGACCAGTTTCTTAGGCTTTCCTCAATAAGAACACAAGCTCAGGAAAGGGAAAAATCTACGTTTTTATTGCTCACATAATCAAACTGAACTTCAGAGTTAAAACGAGAAGGCCAGGCGTGGTGGCTCACACCTGT... |
Subsets and Splits
No community queries yet
The top public SQL queries from the community will appear here once available.