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_42500 | A mutation has occurred on Chromosome 12. What is the medical relevance of this mutation? | Benign | AAATATTAATAACAGCTTTAGTTGTAATAATAAAAAATTGGAAGCAATCCAAATGTCCTTCAACAGGTAAATGAATAAACAAACTGTGGTACGTCCATACAATTGAAATTATTCAGCAATAAAAAGGAACTACAGATATACGCCACAACATGGATAAATCTCAAAATCATGATGCTGTGAAAGAAGCTAAGCTAAAAAGGAGCCATTGCTCATAGGTCCTAGCTCTGTTTTTGGCTCATGCTGTGAATTCTCCCTCCTCTCAACTCTCCAGGGCCCAATTTTCATCTCCAATTATGAAAGTTTTTCCTGGCCTTCAAAAT... | AAATATTAATAACAGCTTTAGTTGTAATAATAAAAAATTGGAAGCAATCCAAATGTCCTTCAACAGGTAAATGAATAAACAAACTGTGGTACGTCCATACAATTGAAATTATTCAGCAATAAAAAGGAACTACAGATATACGCCACAACATGGATAAATCTCAAAATCATGATGCTGTGAAAGAAGCTAAGCTAAAAAGGAGCCATTGCTCATAGGTCCTAGCTCTGTTTTTGGCTCATGCTGTGAATTCTCCCTCCTCTCAACTCTCCAGGGCCCAATTTTCATCTCCAATTATGAAAGTTTTTCCTGGCCTTCAAAAT... |
Task1_train_42501 | This variant is found on Chromosome 12. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TTTTAGTAGAGACGGGGTTTCTCCATATTGGTCATGCTGGTCTTGAACTCCCAACCTCAGGTGATCGGCCCACCTCAGCCTCCCAACGTATTGGGATTACAGGCTTGAGCCACTGCACCCGGCCTTGGTTGTTTTCTTTAATTAATTTTTTATAGAGACGGGGTCTTGCTATGTTAGTCAGGCTGGTCTCAAACTCATGGCCTCAAGTGATCCTCCTGCCCTGGCCTCCCAAAGTGCTGGGATCATAGGCGTATGTGCTGGGACTATAACATCATGCCTGCTAGCTATTTCTTTAGAAAAATGAGAAGAAGGCCGGGCGT... | TTTTAGTAGAGACGGGGTTTCTCCATATTGGTCATGCTGGTCTTGAACTCCCAACCTCAGGTGATCGGCCCACCTCAGCCTCCCAACGTATTGGGATTACAGGCTTGAGCCACTGCACCCGGCCTTGGTTGTTTTCTTTAATTAATTTTTTATAGAGACGGGGTCTTGCTATGTTAGTCAGGCTGGTCTCAAACTCATGGCCTCAAGTGATCCTCCTGCCCTGGCCTCCCAAAGTGCTGGGATCATAGGCGTATGTGCTGGGACTATAACATCATGCCTGCTAGCTATTTCTTTAGAAAAATGAGAAGAAGGCCGGGCGT... |
Task1_train_42502 | A mutation on Chromosome 12 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GCCTGTTGGGTACAGTGTTTGGTTTAGAGTTGTGCTCAAGAAACAGTAATTCTGAGGCCAGGCAAAATGGCTCATGCCTGTAATCCCAGCACTTTAGGAGGCCGAGGTGGGTGGATCACTTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAATATGGCAAAACTCCATCTCTACTAAAATACAAAAATTAGCTGGGCATGGTGGCAGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCCAAGATTGCGCCACTGCTCTCCAGCCTGGGCAACAG... | GCCTGTTGGGTACAGTGTTTGGTTTAGAGTTGTGCTCAAGAAACAGTAATTCTGAGGCCAGGCAAAATGGCTCATGCCTGTAATCCCAGCACTTTAGGAGGCCGAGGTGGGTGGATCACTTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAATATGGCAAAACTCCATCTCTACTAAAATACAAAAATTAGCTGGGCATGGTGGCAGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCCAAGATTGCGCCACTGCTCTCCAGCCTGGGCAACAG... |
Task1_train_42503 | Here is a genetic alteration on Chromosome 12. Based on the data, is it a benign variant or a cause of disease? | Benign | GCATTTAGTCATTATTTCTCTCTTCCTCCCTTTTTAACTTTATTATTTATTTATTTATTTGAGACAGAGTCTCACTCGGTCACTCAGGCTGGAGTGCAGTGACATGATCTCAGCTCATTGCAACCTCTGCCTCCCCGGTTCAAGCGATTCTCCTGCGTCAGCCTCCCAGGTAGCTGGGATTACAAGTGTGTGGCACTGTGCCTTGGTAACTTTTGTATTTTTAGTAGAGACGGTGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAAGTGATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAG... | GCATTTAGTCATTATTTCTCTCTTCCTCCCTTTTTAACTTTATTATTTATTTATTTATTTGAGACAGAGTCTCACTCGGTCACTCAGGCTGGAGTGCAGTGACATGATCTCAGCTCATTGCAACCTCTGCCTCCCCGGTTCAAGCGATTCTCCTGCGTCAGCCTCCCAGGTAGCTGGGATTACAAGTGTGTGGCACTGTGCCTTGGTAACTTTTGTATTTTTAGTAGAGACGGTGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAAGTGATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAG... |
Task1_train_42504 | This mutation is located on Chromosome 12. Is it associated with a disease or is it a benign polymorphism? | Benign | TTAATAGTGTCATTTGATACATAGAAGTTTTAGATTTTGATGGCATCTTGTTTTATTTATTTATTTTTATTTTTTTGAGACAGGGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGTGCAGTCACAGCTCACTGCAGCCTTGACCTCCCTTGAGCAATCCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTATAGGTGCACACCACCATGCCTCGCTAATTTTTATACTTTTTGTAGAGTCAGGGTTTCACCATGCCCAGCCTGGTCTTCAACTCCTGGGCTCAAGTGATCTTCCTGCCTCCCAAAGTGCTGGGATTA... | TTAATAGTGTCATTTGATACATAGAAGTTTTAGATTTTGATGGCATCTTGTTTTATTTATTTATTTTTATTTTTTTGAGACAGGGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGTGCAGTCACAGCTCACTGCAGCCTTGACCTCCCTTGAGCAATCCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTATAGGTGCACACCACCATGCCTCGCTAATTTTTATACTTTTTGTAGAGTCAGGGTTTCACCATGCCCAGCCTGGTCTTCAACTCCTGGGCTCAAGTGATCTTCCTGCCTCCCAAAGTGCTGGGATTA... |
Task1_train_42505 | This alteration on Chromosome 12 may affect genome function. Does it lead to a disease or is it benign? | Benign | CATACACACGCACACACACACACATGATTAGGATGATGCGATTGTTTTGCAGTGTGCTTTTTTCACAAATTTTGGTCACTTTCCCAATCTACCTCATTCTTTTTGAAGGCAGCAAAGTTTTTATTTTTATTTCTATTTTTTATTTTTATGTCTTTATTTTTTTTTGAGATGGAGTTTCACTTTTGTTCCCCGGCTGGAGTGCAATGGTGTAATCTTGGCTCACTGCAAACTCCGCCTCCTGGGTTCAAGTGATTCTCCTACCTCAGCTTCCCGAGTAGCTGGGATTATAGGTGCCTACCACCACACCTGGCTAATTTTTT... | CATACACACGCACACACACACACATGATTAGGATGATGCGATTGTTTTGCAGTGTGCTTTTTTCACAAATTTTGGTCACTTTCCCAATCTACCTCATTCTTTTTGAAGGCAGCAAAGTTTTTATTTTTATTTCTATTTTTTATTTTTATGTCTTTATTTTTTTTTGAGATGGAGTTTCACTTTTGTTCCCCGGCTGGAGTGCAATGGTGTAATCTTGGCTCACTGCAAACTCCGCCTCCTGGGTTCAAGTGATTCTCCTACCTCAGCTTCCCGAGTAGCTGGGATTATAGGTGCCTACCACCACACCTGGCTAATTTTTT... |
Task1_train_42506 | This mutation on Chromosome 12 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GCTAATTTTTCATAGAGACAGGAAACTACTATGTTGCCCAGGCTGGACTCGAACTCCTAACCCCAAGCAATCCTCCCACCTTAGCCTCCCAAAGTGCTGGGATTATGGGAATGAGCCACTGCGTTCTGCCCATGACCAGAGTCTTAAAACCTATGTTGAGATTTATGGAATTTTAAAAACTCTTCCCTTCCCTCCCCTCCCCTCCCCTCCCCTTCCCTCCCCTCCCCTCCCCTCTCCTTCCCTCCCCTTCCCTCCCCTCCCCTTCCCTCCCCTCCCCTCCCCTTCCCTCCCCTCCCCCTCCCCCTCCCCTTCTTCTTCCT... | GCTAATTTTTCATAGAGACAGGAAACTACTATGTTGCCCAGGCTGGACTCGAACTCCTAACCCCAAGCAATCCTCCCACCTTAGCCTCCCAAAGTGCTGGGATTATGGGAATGAGCCACTGCGTTCTGCCCATGACCAGAGTCTTAAAACCTATGTTGAGATTTATGGAATTTTAAAAACTCTTCCCTTCCCTCCCCTCCCCTCCCCTCCCCTTCCCTCCCCTCCCCTCCCCTCTCCTTCCCTCCCCTTCCCTCCCCTCCCCTTCCCTCCCCTCCCCTCCCCTTCCCTCCCCTCCCCCTCCCCCTCCCCTTCTTCTTCCT... |
Task1_train_42507 | Here is a mutation located on Chromosome 12. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TGACGTGTTGAGCCTGCCAGTCCACAGAAGTCAAGAATTGGGGTTTGGGAACCTCTGCCTAGATTTCAGAAGGTGTATGGAAACACCTTGATGCCCAGGCAGAAGTTTGTTGCAGGGGCGGGGCCCTCATGGAGCACCTCTGCTAGAGCAGTGTGGAAGGGAAATGTGGGGTCAGAGCCCCCACACAGAGTCTCTACTGGGGCACTGCCTAGTGGAGCTGTGAGAAGAGGGCCACCATCCTCCAGACCTCAGGATGGTAGATCCACTGACAGCTTGCACTGTTTGCCTGGAAAAGCCATAGACACTAATGCCAGCCCATG... | TGACGTGTTGAGCCTGCCAGTCCACAGAAGTCAAGAATTGGGGTTTGGGAACCTCTGCCTAGATTTCAGAAGGTGTATGGAAACACCTTGATGCCCAGGCAGAAGTTTGTTGCAGGGGCGGGGCCCTCATGGAGCACCTCTGCTAGAGCAGTGTGGAAGGGAAATGTGGGGTCAGAGCCCCCACACAGAGTCTCTACTGGGGCACTGCCTAGTGGAGCTGTGAGAAGAGGGCCACCATCCTCCAGACCTCAGGATGGTAGATCCACTGACAGCTTGCACTGTTTGCCTGGAAAAGCCATAGACACTAATGCCAGCCCATG... |
Task1_train_42508 | A mutation on Chromosome 12 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CAAGCTCCGCCTGCCGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACCCGCCACCATGCCCGGCTAATTATTTTGTATTTTTAGTAGAGACGGGGTTTCACTGTGTTAGCCAGGATGGTCTCCATCTCCTGACCTCGTGATCCGCCCGTCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTGCCCGGCCTAATTTTTTTATTTTAATTTTTTTATTTTAATTTTTTATTTTAATTTTTTTTTGAGATGGAGTTTCACTCTGTTGCCCAGGCTAGAGTGCTGTGCGTG... | CAAGCTCCGCCTGCCGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACCCGCCACCATGCCCGGCTAATTATTTTGTATTTTTAGTAGAGACGGGGTTTCACTGTGTTAGCCAGGATGGTCTCCATCTCCTGACCTCGTGATCCGCCCGTCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTGCCCGGCCTAATTTTTTTATTTTAATTTTTTTATTTTAATTTTTTATTTTAATTTTTTTTTGAGATGGAGTTTCACTCTGTTGCCCAGGCTAGAGTGCTGTGCGTG... |
Task1_train_42509 | A mutation has occurred on Chromosome 12. What is the medical relevance of this mutation? | Benign | CTGCTGTGCGCCCTTCTCGGTGAATGGCACCGCCGCCCGCCCGGGCCTCTCGTCCACAGCCCGCGGTGCTCGCACACCTGAGACTCATCTCGCTTCGACCCCGCCGCCGCCGCCGCCCGGCATCCTGAGCACGGAGACAGTCTCCAGCTGCCGTTCATGCTTCCTCCCCAGCCTTCCGCAGCCCACCAGGGAAGGGGCGGTAGGAGTGGCCTTTTACCAAAGGTCAGATTCTTTCACCGCCTCTGCCAGACCCCCTTGTCCCCCACCCCCGCATAGATCTCCAGGGGGCTCAGAAAACTCTGGCCGGTGGCTCACGCCTG... | CTGCTGTGCGCCCTTCTCGGTGAATGGCACCGCCGCCCGCCCGGGCCTCTCGTCCACAGCCCGCGGTGCTCGCACACCTGAGACTCATCTCGCTTCGACCCCGCCGCCGCCGCCGCCCGGCATCCTGAGCACGGAGACAGTCTCCAGCTGCCGTTCATGCTTCCTCCCCAGCCTTCCGCAGCCCACCAGGGAAGGGGCGGTAGGAGTGGCCTTTTACCAAAGGTCAGATTCTTTCACCGCCTCTGCCAGACCCCCTTGTCCCCCACCCCCGCATAGATCTCCAGGGGGCTCAGAAAACTCTGGCCGGTGGCTCACGCCTG... |
Task1_train_42510 | A mutation has occurred on Chromosome 12. What is the medical relevance of this mutation? | Benign | CAGTGATCAGGCCAAGTCACTGGAGCCCAAGGCCGCTGAGAATACAATTGGTCACTCCATATGCCTGTCTGGACACGTCTGTCTCTAAGGACACGCTTCTGAGAGGCTACCAGATGTCTACTCCATTTCAATAGTATCAACAACTAATCTAGCAAAAAGTATCAGTAATTGTTTTATGTTAGGAATTTTCATAAAGTGAATAATTTAAAATTTGTTAATAGAGCTATTTAAAGGAGTTATATAAGAAACTCTTTCAAAAGAGCAAATACCTTATCTAATACAGTCTTAAAAAGATTTGATTTTAGGGGCCAGGTCTCATG... | CAGTGATCAGGCCAAGTCACTGGAGCCCAAGGCCGCTGAGAATACAATTGGTCACTCCATATGCCTGTCTGGACACGTCTGTCTCTAAGGACACGCTTCTGAGAGGCTACCAGATGTCTACTCCATTTCAATAGTATCAACAACTAATCTAGCAAAAAGTATCAGTAATTGTTTTATGTTAGGAATTTTCATAAAGTGAATAATTTAAAATTTGTTAATAGAGCTATTTAAAGGAGTTATATAAGAAACTCTTTCAAAAGAGCAAATACCTTATCTAATACAGTCTTAAAAAGATTTGATTTTAGGGGCCAGGTCTCATG... |
Task1_train_42511 | A mutation on Chromosome 12 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CGAGGCAGGCAGATCACAAGGTCAGGAGTCAATATGGTGAAACCCAGTCCCTACTAAAAATACAAAGCTTAGCCGGGTGTGGCAGCACGCACCTGTAGTCCCAGCTACTCAAGAGGGTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCCAAGGTCACACCACTGTACTCCAACCTGGGTGACAGAGCGAGACTCTTTTTTTTTTTTTTAGGCAGTCTCATTCTGTCACCAGGCTGGAGCGCAGTGGTGCAATCTCAGCTCACTGCAACCTCCGCCTCCCTGGTTCAAGTGATTCTCCTGCCTC... | CGAGGCAGGCAGATCACAAGGTCAGGAGTCAATATGGTGAAACCCAGTCCCTACTAAAAATACAAAGCTTAGCCGGGTGTGGCAGCACGCACCTGTAGTCCCAGCTACTCAAGAGGGTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCCAAGGTCACACCACTGTACTCCAACCTGGGTGACAGAGCGAGACTCTTTTTTTTTTTTTTAGGCAGTCTCATTCTGTCACCAGGCTGGAGCGCAGTGGTGCAATCTCAGCTCACTGCAACCTCCGCCTCCCTGGTTCAAGTGATTCTCCTGCCTC... |
Task1_train_42512 | A mutation has occurred on Chromosome 12. What is the medical relevance of this mutation? | Benign | ATCTCAGCTCACTGCAACCTCCGCCTCCCTGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGAACTACAGGCCCACATCACCACACCGGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGATGGTCTTGATCTTCTGATCTCGTGATCCGCCTGCAACAGCCTCCCAAAGTGCTGGGATTACAGGTGTAAGCCACCGCACCCGGTGAGACTCTGTCTTAAATAAATAAATAAATAAATAAATAAATAAATAAATAAAGTCCTTTAGGCACTTGTTTATAATTTATTGGTCTA... | ATCTCAGCTCACTGCAACCTCCGCCTCCCTGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGAACTACAGGCCCACATCACCACACCGGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGATGGTCTTGATCTTCTGATCTCGTGATCCGCCTGCAACAGCCTCCCAAAGTGCTGGGATTACAGGTGTAAGCCACCGCACCCGGTGAGACTCTGTCTTAAATAAATAAATAAATAAATAAATAAATAAATAAATAAAGTCCTTTAGGCACTTGTTTATAATTTATTGGTCTA... |
Task1_train_42513 | This variant is located on Chromosome 12. Evaluate its biological effect and specify any disease association. | Benign | GGATTACAGGTGTAAGCCACCGCACCCGGTGAGACTCTGTCTTAAATAAATAAATAAATAAATAAATAAATAAATAAATAAAGTCCTTTAGGCACTTGTTTATAATTTATTGGTCTAATAAAGTTTATGAAAATTCTGCATTTTTCCCTATCCAATTATCAGCCATGAAGATTTCAATGGAATCTTCCAACTCCAAATGGACAGACACAATGAAATAGTTAAAAGCCAAACAGAAGACTATATTTCAATATGTGCCAATTTATTGCTTTTTTTTTTTTTCCCTTGAGACAGAGTTTTTCACTCTTGTTGCCCAGGCTGGA... | GGATTACAGGTGTAAGCCACCGCACCCGGTGAGACTCTGTCTTAAATAAATAAATAAATAAATAAATAAATAAATAAATAAAGTCCTTTAGGCACTTGTTTATAATTTATTGGTCTAATAAAGTTTATGAAAATTCTGCATTTTTCCCTATCCAATTATCAGCCATGAAGATTTCAATGGAATCTTCCAACTCCAAATGGACAGACACAATGAAATAGTTAAAAGCCAAACAGAAGACTATATTTCAATATGTGCCAATTTATTGCTTTTTTTTTTTTTCCCTTGAGACAGAGTTTTTCACTCTTGTTGCCCAGGCTGGA... |
Task1_train_42514 | Given this variant on Chromosome 12, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCAGAACTGGCTACAAATTTACATTTGAATGGCCTCACATGGCTGGTGGCTACTACATTAGGCAGCACAGCTATAGCCCACTGGCTCTTAAAAGTAGGGAATAGGAGGCTTCATGGGTTCCAGGAACCTTGTTGAGTGCACACGTAAACTTTCCTGAAAAAATATCTGTAGATTTCATTAGATTATTCCAAAGAGTCTGGGACTGATTACGATCCACTGAAATTAGATACTAGACACGTTTGGAGGGGAACAGTCCTGGCATTTTTAACTCAATGACTCTTGCACAA... | CTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCAGAACTGGCTACAAATTTACATTTGAATGGCCTCACATGGCTGGTGGCTACTACATTAGGCAGCACAGCTATAGCCCACTGGCTCTTAAAAGTAGGGAATAGGAGGCTTCATGGGTTCCAGGAACCTTGTTGAGTGCACACGTAAACTTTCCTGAAAAAATATCTGTAGATTTCATTAGATTATTCCAAAGAGTCTGGGACTGATTACGATCCACTGAAATTAGATACTAGACACGTTTGGAGGGGAACAGTCCTGGCATTTTTAACTCAATGACTCTTGCACAA... |
Task1_train_42515 | A mutation on Chromosome 12 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | AGTTTCGCTCCCTCCCTTCCTTTTTATTATTTATTTATTTTTTTTTTGAGACGGAGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAATGGCACTATCTCAGCTCACCGCAACCTCCACCTCCCGGGTCCAACTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGAATGCGCCACCATACCCGGCTAATTTTGTATCTTTAGTAGAGACGGGGTTTTCCATGTTGGTCAGGCTGTTCTTGAACTCCCAACCTCAGGTGATCCGCCTACCTCGGCCTCCCAAAGTGCAGGGAGATTACAGACATGAGCTACA... | AGTTTCGCTCCCTCCCTTCCTTTTTATTATTTATTTATTTTTTTTTTGAGACGGAGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAATGGCACTATCTCAGCTCACCGCAACCTCCACCTCCCGGGTCCAACTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGAATGCGCCACCATACCCGGCTAATTTTGTATCTTTAGTAGAGACGGGGTTTTCCATGTTGGTCAGGCTGTTCTTGAACTCCCAACCTCAGGTGATCCGCCTACCTCGGCCTCCCAAAGTGCAGGGAGATTACAGACATGAGCTACA... |
Task1_train_42516 | This variant lies on Chromosome 12. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CTGAAAATTATCATACTCTTGGTTGTCTCAGTCTTGTGGCTGGAGATTTAGCAAGTGAAGTTCCTGTGATAATTGGGGTAATTGTTTTTATAAAGTTTTGTTTTTTGTTGCCTAAAGCATTTTCTCAGAAAAATGTTTTTGTTTTGGTTAAATTGCAAAATAATTTGTAACATATAACCGAAACAAGGAAATTATAAAATTAAGGTAATTAAAAATAACTCAATAAATAAATTTCTGTCTTGGAAAAAATATTGCATCTTTACTTTCCCTAGTCTTTACCTGAAAGTACAGCATTTTTTTCAATTATGAGAGCAGACAAA... | CTGAAAATTATCATACTCTTGGTTGTCTCAGTCTTGTGGCTGGAGATTTAGCAAGTGAAGTTCCTGTGATAATTGGGGTAATTGTTTTTATAAAGTTTTGTTTTTTGTTGCCTAAAGCATTTTCTCAGAAAAATGTTTTTGTTTTGGTTAAATTGCAAAATAATTTGTAACATATAACCGAAACAAGGAAATTATAAAATTAAGGTAATTAAAAATAACTCAATAAATAAATTTCTGTCTTGGAAAAAATATTGCATCTTTACTTTCCCTAGTCTTTACCTGAAAGTACAGCATTTTTTTCAATTATGAGAGCAGACAAA... |
Task1_train_42517 | This mutation is located on Chromosome 12. Is it associated with a disease or is it a benign polymorphism? | Benign | CACTGCGCCTGAACAAGAATTTTTAGAACTAAGATAAAATGTGTTATTTATAGATTCCGCTGACTTTGATAAGTAGGGATAAATGATTTGTAATTTATATCTCAGATGTTTCTGTCTAGTAAATACAAGGACTCGTTTTCTGGTTTCAGAATGCTTTCAGATCTGTCACCTCATTTAATTTTTATAGTTCTTATTGCATATGTTGCCAGTTGATATATGAGAAAACAACATAGTATGTGACCTGCTCAAGGTCAAATTATTAATGACTGCTTCTAAAATATTATGGGTGCTATAACCTCCATCTGATTTGTAACAGATTA... | CACTGCGCCTGAACAAGAATTTTTAGAACTAAGATAAAATGTGTTATTTATAGATTCCGCTGACTTTGATAAGTAGGGATAAATGATTTGTAATTTATATCTCAGATGTTTCTGTCTAGTAAATACAAGGACTCGTTTTCTGGTTTCAGAATGCTTTCAGATCTGTCACCTCATTTAATTTTTATAGTTCTTATTGCATATGTTGCCAGTTGATATATGAGAAAACAACATAGTATGTGACCTGCTCAAGGTCAAATTATTAATGACTGCTTCTAAAATATTATGGGTGCTATAACCTCCATCTGATTTGTAACAGATTA... |
Task1_train_42518 | Here is a variant on Chromosome 12. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GATCTCGGCTCATTGCAAGCTCCGCCTGCTGGGTTCACGCTATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCATGCCGCCACGCCCTGCTAATTTTTGTATTTTTAATAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTTGTGATCCGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCACCCGGCCGAGATTTCCTGTTTTACAGGCATGTATGCTATGTGTGTGCATATCTACAGTGTATATATGCATTTTTGCACACATAAATGCAATC... | GATCTCGGCTCATTGCAAGCTCCGCCTGCTGGGTTCACGCTATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCATGCCGCCACGCCCTGCTAATTTTTGTATTTTTAATAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTTGTGATCCGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCACCCGGCCGAGATTTCCTGTTTTACAGGCATGTATGCTATGTGTGTGCATATCTACAGTGTATATATGCATTTTTGCACACATAAATGCAATC... |
Task1_train_42519 | A genetic alteration is present on Chromosome 12. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TCCTTGCTTTTGGCTTTTTACCTGTACATTGCTTGGTGATACAGACAAGCCAACTGCTCTGAAAGCACAGAGGTAATTCCAGAGCATCCACCTTTCTTCATTTACTGTCATTCACCCAGAGCTGGGAGCCTGTCTCTAAATTCCTTATCTGTGTTCATGTCAGGAGGTTGAAGCAAGCCTCGTCTTGCCAAATAATCAAGGACTGACAGAGTTAGAAATGAAAGCGTAACAGAAACTTGGACTGATCACAGACTCAAACCAGTACATCTCCTTTCCTTCTCTGAATTGGGAACTGAAACCATTCCATAGGAAGCTCGCTC... | TCCTTGCTTTTGGCTTTTTACCTGTACATTGCTTGGTGATACAGACAAGCCAACTGCTCTGAAAGCACAGAGGTAATTCCAGAGCATCCACCTTTCTTCATTTACTGTCATTCACCCAGAGCTGGGAGCCTGTCTCTAAATTCCTTATCTGTGTTCATGTCAGGAGGTTGAAGCAAGCCTCGTCTTGCCAAATAATCAAGGACTGACAGAGTTAGAAATGAAAGCGTAACAGAAACTTGGACTGATCACAGACTCAAACCAGTACATCTCCTTTCCTTCTCTGAATTGGGAACTGAAACCATTCCATAGGAAGCTCGCTC... |
Task1_train_42520 | Here’s a variant located on Chromosome 12. What is the predicted biological effect — harmless or disease-causing? | Benign | TCCCTTGAACGAATCCGCGTTTCACAACGAGGCTCCCCACTGACTCATGCCTCCGAGGCTGGGGAATCCCTATTTTCCTCTGAGCTCATCCCTGACATCTCTTCCTCTTTAAGGTGATCCTTGCTTTTGGCTTTTTACCTGTACATTGCTTGGTGATACAGACAAGCCAACTGCTCTGAAAGCACAGAGGTAATTCCAGAGCATCCACCTTTCTTCATTTACTGTCATTCACCCAGAGCTGGGAGCCTGTCTCTAAATTCCTTATCTGTGTTCATGTCAGGAGGTTGAAGCAAGCCTCGTCTTGCCAAATAATCAAGGAC... | TCCCTTGAACGAATCCGCGTTTCACAACGAGGCTCCCCACTGACTCATGCCTCCGAGGCTGGGGAATCCCTATTTTCCTCTGAGCTCATCCCTGACATCTCTTCCTCTTTAAGGTGATCCTTGCTTTTGGCTTTTTACCTGTACATTGCTTGGTGATACAGACAAGCCAACTGCTCTGAAAGCACAGAGGTAATTCCAGAGCATCCACCTTTCTTCATTTACTGTCATTCACCCAGAGCTGGGAGCCTGTCTCTAAATTCCTTATCTGTGTTCATGTCAGGAGGTTGAAGCAAGCCTCGTCTTGCCAAATAATCAAGGAC... |
Task1_train_42521 | Assess the clinical impact of this variant found on Chromosome 12. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CTATGGAAAAATATCTGCCTGGCTTGATTCCCTTTTTATATTATTTATTATTATTATTTGAGATGAAGTCTTGCTCTGTCCCCCAGGCTGGAGTGCAGGCACACCACCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCAATTCTTCTTCTCCCAGCCTTCCCAGTAGCTGGGACTACAAGCGGCCGCCACCATGCCTGGCTAATTTTTCTTGTATTTTTAGTAGAAGTGGGGTTTCACCATTTTGTCCAGGCTGGTCTCAAACTCCTTACTTCAGGTGATCTGCCCGCCTTGGCTCCCCCAAAGTGCTGGGATT... | CTATGGAAAAATATCTGCCTGGCTTGATTCCCTTTTTATATTATTTATTATTATTATTTGAGATGAAGTCTTGCTCTGTCCCCCAGGCTGGAGTGCAGGCACACCACCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCAATTCTTCTTCTCCCAGCCTTCCCAGTAGCTGGGACTACAAGCGGCCGCCACCATGCCTGGCTAATTTTTCTTGTATTTTTAGTAGAAGTGGGGTTTCACCATTTTGTCCAGGCTGGTCTCAAACTCCTTACTTCAGGTGATCTGCCCGCCTTGGCTCCCCCAAAGTGCTGGGATT... |
Task1_train_42522 | Consider this mutation on Chromosome 12. Is this a benign change or a disease-causing variant? | Benign | AGTCGTACTCTGCCGTGTGGACAGACCACATTGTGTTTATCTGTTCATCACTTGGTGGACATTGGGTTTGTTGCAACTTTCTGGCTGTTGTAAATAGTGCTGCTGTGGGCCTTTGAGCACAAGTTTCTGTGTAAACATCTGCCATCACTTATCTTGGATAGATAGCTGATGTGTGTGGAACACAGTAGAACTGCTGGGTCTCACCTCTGTTACCCTGTTGAGAAACTACCAGACTGTTTTCCAAAGTGGCTGCACCATTTTACACTCCCACCAGCAACGCATGAATGTTCCAGTTTCTCCACATCCTTGCCAATGCTTAT... | AGTCGTACTCTGCCGTGTGGACAGACCACATTGTGTTTATCTGTTCATCACTTGGTGGACATTGGGTTTGTTGCAACTTTCTGGCTGTTGTAAATAGTGCTGCTGTGGGCCTTTGAGCACAAGTTTCTGTGTAAACATCTGCCATCACTTATCTTGGATAGATAGCTGATGTGTGTGGAACACAGTAGAACTGCTGGGTCTCACCTCTGTTACCCTGTTGAGAAACTACCAGACTGTTTTCCAAAGTGGCTGCACCATTTTACACTCCCACCAGCAACGCATGAATGTTCCAGTTTCTCCACATCCTTGCCAATGCTTAT... |
Task1_train_42523 | A variant was discovered on Chromosome 12. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GTGAATAACTTCCCAGACACTTATCTCCAGGGCAGGGTGCCTTCCAGTAGCCAAGGGAAGCCTCCAGAGAGCACAGATGTGAACCCTCAGCAGCAGGCATCACCCCCCAGTGGACTCGGGTGGGCCACCAGTAGCATCTTCTAGATGGCAGAGGGGTGAATGGCAGGGCCAGGAACCAGGCTGCCCGGGTTCCCATTCTGCTTCTGCCACTTCCAGCTGTGTGGCTTTAGGTGAGCCTTCACCTTTTGGTGCCTTCGTTTCCTCATTTAGCACCTACCTCCTAGAGCTGTTTTGGGAGTCAAATGCGCTGACGTATATAA... | GTGAATAACTTCCCAGACACTTATCTCCAGGGCAGGGTGCCTTCCAGTAGCCAAGGGAAGCCTCCAGAGAGCACAGATGTGAACCCTCAGCAGCAGGCATCACCCCCCAGTGGACTCGGGTGGGCCACCAGTAGCATCTTCTAGATGGCAGAGGGGTGAATGGCAGGGCCAGGAACCAGGCTGCCCGGGTTCCCATTCTGCTTCTGCCACTTCCAGCTGTGTGGCTTTAGGTGAGCCTTCACCTTTTGGTGCCTTCGTTTCCTCATTTAGCACCTACCTCCTAGAGCTGTTTTGGGAGTCAAATGCGCTGACGTATATAA... |
Task1_train_42524 | Chromosome 12 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GTCTCAAACTCCAGAGCTCAAGTGATCTGCCCACCTTGGCCTCCCAAAGTGCTGGAATTACAGGCCTGAGCCACTGCACCCAGCCAATACTTACTATATTCAATGATAAAATAATAAAAACACGTACAATATTCAGTATGTACAATTACTAAAAAATACAGAATGACAATACTCAATGGACATGACTTATATTAAAAGGAAAAAGACTCTTCTAAAGCTTAATCTAAATATACAGGCATTGTTCTTTTCACTGAGAAGCATCTCAGTAAAACATACCTTATCTCCATCCATAAATCGTTGTTTTTCTGTGATGTTTAGTA... | GTCTCAAACTCCAGAGCTCAAGTGATCTGCCCACCTTGGCCTCCCAAAGTGCTGGAATTACAGGCCTGAGCCACTGCACCCAGCCAATACTTACTATATTCAATGATAAAATAATAAAAACACGTACAATATTCAGTATGTACAATTACTAAAAAATACAGAATGACAATACTCAATGGACATGACTTATATTAAAAGGAAAAAGACTCTTCTAAAGCTTAATCTAAATATACAGGCATTGTTCTTTTCACTGAGAAGCATCTCAGTAAAACATACCTTATCTCCATCCATAAATCGTTGTTTTTCTGTGATGTTTAGTA... |
Task1_train_42525 | 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 | CCACAGTCCTTTTCAGTGCCATATATGTTTTTATAAATTTATATATATATATAAATATATGTATATATATGTGTGTATATATATTAATATATATACACACATATGTGTATATATATATTAATATATATACACACATATGTGTATATATATACACACATATGTGTATATATATACACATATATGTATATATATAAATATATATATATACACACATATATGTATATATATATAAATATATATATACACACATATATGTATATATATAAAAATATATATATACACACATATATGTGTATATATACTTTTTTTTTTGAGACATA... | CCACAGTCCTTTTCAGTGCCATATATGTTTTTATAAATTTATATATATATATAAATATATGTATATATATGTGTGTATATATATTAATATATATACACACATATGTGTATATATATATTAATATATATACACACATATGTGTATATATATACACACATATGTGTATATATATACACATATATGTATATATATAAATATATATATATACACACATATATGTATATATATATAAATATATATATACACACATATATGTATATATATAAAAATATATATATACACACATATATGTGTATATATACTTTTTTTTTTGAGACATA... |
Task1_train_42526 | Assess the clinical impact of this variant found on Chromosome 12. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TTACAAGAATGAGCCATCATGCCTGGCCCAAATATGCTGAATTTCTAGTAGTAAATACTGGCTGCTGGCTTCTGTAGTTTCTTCACAAAGAAGTAGATGGGCTTTTGGCAACTTGATTGTTTAGTAATGAGGCCACTCCTCACCCCTGTTCTGTTCTGTCCCATTGCTGGGATGGGCCAGGAGGCACAAATGTAGAGAGCACAGGCTGCAGGGGAGGCAGCACCATCAGGGCGAGGAGGCACCCACAGGCCAGTGCCACTGCTGACGGTACACTGGCCCACCAGCCCGGGGCTGGGGCTTTTCTTTCTCTTTTGCAATAA... | TTACAAGAATGAGCCATCATGCCTGGCCCAAATATGCTGAATTTCTAGTAGTAAATACTGGCTGCTGGCTTCTGTAGTTTCTTCACAAAGAAGTAGATGGGCTTTTGGCAACTTGATTGTTTAGTAATGAGGCCACTCCTCACCCCTGTTCTGTTCTGTCCCATTGCTGGGATGGGCCAGGAGGCACAAATGTAGAGAGCACAGGCTGCAGGGGAGGCAGCACCATCAGGGCGAGGAGGCACCCACAGGCCAGTGCCACTGCTGACGGTACACTGGCCCACCAGCCCGGGGCTGGGGCTTTTCTTTCTCTTTTGCAATAA... |
Task1_train_42527 | This sequence change occurs on Chromosome 12. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TTACGAATTGCAAACTCACTGGGGCTGGGCTGGTGGTGGCAGTGGGGGGCCCTGGTGGGGTTTTTTTTTTTTTTTTTTGAGACGGAGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAATGGCACTATCTCGGTTCACCGCAACCTCCACCTCCCGGGTTCAATGGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCGCCACCCCAGCTAATTTTGTATTTTTAGTAGAGATGGGGTTTCTCCATGTTGGTCAGGCTGGTCTTGAACTCCCGACCTCAGGTGATCCGCCCACCTCGGCCTCCCAAAG... | TTACGAATTGCAAACTCACTGGGGCTGGGCTGGTGGTGGCAGTGGGGGGCCCTGGTGGGGTTTTTTTTTTTTTTTTTTGAGACGGAGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAATGGCACTATCTCGGTTCACCGCAACCTCCACCTCCCGGGTTCAATGGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCGCCACCCCAGCTAATTTTGTATTTTTAGTAGAGATGGGGTTTCTCCATGTTGGTCAGGCTGGTCTTGAACTCCCGACCTCAGGTGATCCGCCCACCTCGGCCTCCCAAAG... |
Task1_train_42528 | A variant was discovered on Chromosome 12. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CTGTACTATCAGAGGAGCCTCAGGGTCCTAGGATCGGAGCTAGGGTTTTCAGTGTAAATGGAAGCACTGCTGTGTTAAAGCGAGAAAGCTGTGTTTATGAAATGAATAGATGAATGATTGTTGGGAAAAACTATTAACATGGACAGGAAACCTTAGTGTCAGCAACCAGGAGAGCTTGAGTGTTTTGTGTCTTTGGAAAACTCTGAAGATAGCAAAAGTTTGGAAAAAGAGGACCAAATTCAAAAGAGTTTTATTTTTATTTTATTTTATTTTATTTTTAGACAGAGTCTTGCTCTTGCCCAGGCTGGAATGCAGTGGCA... | CTGTACTATCAGAGGAGCCTCAGGGTCCTAGGATCGGAGCTAGGGTTTTCAGTGTAAATGGAAGCACTGCTGTGTTAAAGCGAGAAAGCTGTGTTTATGAAATGAATAGATGAATGATTGTTGGGAAAAACTATTAACATGGACAGGAAACCTTAGTGTCAGCAACCAGGAGAGCTTGAGTGTTTTGTGTCTTTGGAAAACTCTGAAGATAGCAAAAGTTTGGAAAAAGAGGACCAAATTCAAAAGAGTTTTATTTTTATTTTATTTTATTTTATTTTTAGACAGAGTCTTGCTCTTGCCCAGGCTGGAATGCAGTGGCA... |
Task1_train_42529 | Here is a mutation located on Chromosome 12. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GCGAATTCAGAATCCTAACTCTGGGAAAGCGCTCTCTGGAAATGTAGTTTGATAATAGTGTCTTATAGGGGCCACGGGAATTTGTTTCTCTATAAAGCGATGGGCTCCAGTGTCATGTTACCAGAGTTATCGCTCAGTTTTGTTTGTTAAGGCTTTTGCTAGAACCTATTATGTATCCAGTTTTTAAAACATACTTCATTCCCTTGATAGCAGAGATCCAGAGCACAGATGGCAAGTTGTGTGGATGATACTGAATATGTTTATTTTCCTAAAGATAAATGTCACGACACGACATTTCTCAGTTTTTATTTAGATGTTTA... | GCGAATTCAGAATCCTAACTCTGGGAAAGCGCTCTCTGGAAATGTAGTTTGATAATAGTGTCTTATAGGGGCCACGGGAATTTGTTTCTCTATAAAGCGATGGGCTCCAGTGTCATGTTACCAGAGTTATCGCTCAGTTTTGTTTGTTAAGGCTTTTGCTAGAACCTATTATGTATCCAGTTTTTAAAACATACTTCATTCCCTTGATAGCAGAGATCCAGAGCACAGATGGCAAGTTGTGTGGATGATACTGAATATGTTTATTTTCCTAAAGATAAATGTCACGACACGACATTTCTCAGTTTTTATTTAGATGTTTA... |
Task1_train_42530 | Consider a variant on Chromosome 12. Determine its clinical classification and disease relevance. | Benign | ATGGGTTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGCGATTCACCCGCCTCGGCTTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGTGCCCGGCCTAATTTTTTTCTTTTAATTGTAGAGATGGGGTCTCCCTATGTTGCCCCGGCTGTTCTCGAACTCCTGGGCTCAAGAGATTTTCCCGCCTTGGCCTCTCAAAGTGCTGGATTACAGGCATAAGCTACCATGCCCAGCTTTTCAAATCCATGAATTTATAATGATCTTTAAAAGTCCTGATGGGTCATTTCTGGAGGATGATAGGGGACCA... | ATGGGTTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGCGATTCACCCGCCTCGGCTTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGTGCCCGGCCTAATTTTTTTCTTTTAATTGTAGAGATGGGGTCTCCCTATGTTGCCCCGGCTGTTCTCGAACTCCTGGGCTCAAGAGATTTTCCCGCCTTGGCCTCTCAAAGTGCTGGATTACAGGCATAAGCTACCATGCCCAGCTTTTCAAATCCATGAATTTATAATGATCTTTAAAAGTCCTGATGGGTCATTTCTGGAGGATGATAGGGGACCA... |
Task1_train_42531 | A genomic variant on Chromosome 12 is under review. What is the biological outcome — benign or pathogenic? | Benign | TGACACCCGGGCCAAGATAGAGGCTTCGGGGAGGGAAGATCGGTGGGAGTTTGACCGGAAGCGGCTGTTCGAGAGGACGGATTATATGGCCACCATCTGCCAGGACCTCTCCGACGTTCTGCAGGTAGGGGCTGGGCGAAGGCCGGCGGAATTTGCCCCGAAGAAGGCAGTTGGCTTTTGACAGTGGCCCCCTCCGTGTCAGGTAGGAGCTGGGCGTCAGAAAGGGCCTGGCAGGGAGAAGCCCTTCAAAGAAAGAACCTACGGAATATACTAGAATGTACCAGAATGGACCAGAGTACACCAGAGCTTTGCGACTTTTT... | TGACACCCGGGCCAAGATAGAGGCTTCGGGGAGGGAAGATCGGTGGGAGTTTGACCGGAAGCGGCTGTTCGAGAGGACGGATTATATGGCCACCATCTGCCAGGACCTCTCCGACGTTCTGCAGGTAGGGGCTGGGCGAAGGCCGGCGGAATTTGCCCCGAAGAAGGCAGTTGGCTTTTGACAGTGGCCCCCTCCGTGTCAGGTAGGAGCTGGGCGTCAGAAAGGGCCTGGCAGGGAGAAGCCCTTCAAAGAAAGAACCTACGGAATATACTAGAATGTACCAGAATGGACCAGAGTACACCAGAGCTTTGCGACTTTTT... |
Task1_train_42532 | A genomic variant on Chromosome 12 is under review. What is the biological outcome — benign or pathogenic? | Benign | AATCACCTTTACTTTTATTTTTTTAATTAAAAATGTAATTTGGAGGTAATTATAGATTCACATGCAGTTGTTAAGAATTACGACAGAGGGAGCCTTCGTACCCTTTAGTCATTTTCCCTAAGTAGTAACTTCTTGCAAAACTAGTTAAGATCACAACCAAGATATTGACATTGATACAGTCGAGATAGAGAGCATTTTCAACACCACAGCGAGTACTGTCAAGTCCACTTCCCTCCCATCCTTGCCCTCTCCTTAATCCCTGGCAACCATGAATCTTTATTCAATTTCTGTAATGTTGTCATTTCAGAGTGTTATATAAA... | AATCACCTTTACTTTTATTTTTTTAATTAAAAATGTAATTTGGAGGTAATTATAGATTCACATGCAGTTGTTAAGAATTACGACAGAGGGAGCCTTCGTACCCTTTAGTCATTTTCCCTAAGTAGTAACTTCTTGCAAAACTAGTTAAGATCACAACCAAGATATTGACATTGATACAGTCGAGATAGAGAGCATTTTCAACACCACAGCGAGTACTGTCAAGTCCACTTCCCTCCCATCCTTGCCCTCTCCTTAATCCCTGGCAACCATGAATCTTTATTCAATTTCTGTAATGTTGTCATTTCAGAGTGTTATATAAA... |
Task1_train_42533 | 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 | TACAGGTGCACATCACCACACCCGGCTAACTTTTGTATTTTTAGTAGAGACAGGGTTTCGCCATGTTGGCCAGGCTGGTCTCGAACTCCCGACCTCAGGTGATCTGCCGGCCTCGGCCTCCCAAAGCGCTGGGATTACAGGCGTGAGCCAAAGCATTCGGCCTCCTACTCTTTTAAATTTATTTTGCCATTAACTGTAGGTCATCAAGATAATGACTATAGTAATCCGCAGTCACTTTTCCAGTATTGGCATTGTATTACTGTGTTTTCACACTGCTATACAGAAATACTCAAGACTGGGTAATTTATAAAGAAAAAGGT... | TACAGGTGCACATCACCACACCCGGCTAACTTTTGTATTTTTAGTAGAGACAGGGTTTCGCCATGTTGGCCAGGCTGGTCTCGAACTCCCGACCTCAGGTGATCTGCCGGCCTCGGCCTCCCAAAGCGCTGGGATTACAGGCGTGAGCCAAAGCATTCGGCCTCCTACTCTTTTAAATTTATTTTGCCATTAACTGTAGGTCATCAAGATAATGACTATAGTAATCCGCAGTCACTTTTCCAGTATTGGCATTGTATTACTGTGTTTTCACACTGCTATACAGAAATACTCAAGACTGGGTAATTTATAAAGAAAAAGGT... |
Task1_train_42534 | A variant was discovered on Chromosome 12. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TCACTTTTCCAGTATTGGCATTGTATTACTGTGTTTTCACACTGCTATACAGAAATACTCAAGACTGGGTAATTTATAAAGAAAAAGGTTTAATTGACTCACAGTCACGCATGGCTGGGGAGGCCTCAGGAAACTTACAGTCATGGCGGAAGACAAAGGAAAAGCAAGTACCTTTTTCACAAGGTGGCGGGAAAGAGAGAGAGAGAAGGAGGAACTAACAACCACTTATAAAACCGTCAGATCTCATGAGAACTCACTCAGTATCACGAGAACAGCATGGGGAAACCGCCCCCATGATCCAGTCACCTCCCACCAGGTCC... | TCACTTTTCCAGTATTGGCATTGTATTACTGTGTTTTCACACTGCTATACAGAAATACTCAAGACTGGGTAATTTATAAAGAAAAAGGTTTAATTGACTCACAGTCACGCATGGCTGGGGAGGCCTCAGGAAACTTACAGTCATGGCGGAAGACAAAGGAAAAGCAAGTACCTTTTTCACAAGGTGGCGGGAAAGAGAGAGAGAGAAGGAGGAACTAACAACCACTTATAAAACCGTCAGATCTCATGAGAACTCACTCAGTATCACGAGAACAGCATGGGGAAACCGCCCCCATGATCCAGTCACCTCCCACCAGGTCC... |
Task1_train_42535 | A mutation on Chromosome 12 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CATCCGCCAGTGCACGGGAACCTTTGGCTACGGCTACGAGTACATGGGCCTGAACGGCAGGCTGGTCATCACGCCCCTCACCGATCGGATTTACCTGACGCTCACCCAGGTGACTGCCAGCCTGGCACTTGTGGTTACCACTTACCTTGGGGCGGGGCATTTTCTCTAAGCTTGAGGTGTGATGACTGCAGTGATTGAAATAGCAGGGGAGATCATTGCTTTGAAATCTCGAAAAGCTTTTCCATTTGGGATGTGACCAGATTGTCACCATTTGGGATTGGCATGTAAGTGTGGCCGTGCTTAGCCACTGGTACACTGGT... | CATCCGCCAGTGCACGGGAACCTTTGGCTACGGCTACGAGTACATGGGCCTGAACGGCAGGCTGGTCATCACGCCCCTCACCGATCGGATTTACCTGACGCTCACCCAGGTGACTGCCAGCCTGGCACTTGTGGTTACCACTTACCTTGGGGCGGGGCATTTTCTCTAAGCTTGAGGTGTGATGACTGCAGTGATTGAAATAGCAGGGGAGATCATTGCTTTGAAATCTCGAAAAGCTTTTCCATTTGGGATGTGACCAGATTGTCACCATTTGGGATTGGCATGTAAGTGTGGCCGTGCTTAGCCACTGGTACACTGGT... |
Task1_train_42536 | This genomic variant is located on Chromosome 12. Can you determine its pathogenicity and name any linked disease? | Benign | ATCCACCCACCTCAGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACCGCACCCGACCTATTTTGTGGCTTTTGGATATTGTGTCCTAGTTAAAAGGCCTGATCACACTGCAAGATTGTAAAATAATTTCCCCATGATTTCTTTTGGTACTCTTATGTTTTAATTTTTTATATTTAAATCTTTTATCTATTGAGGATTTTTTTCCTGGGGTTCTGTGTGAGTTTGGATCCAATTTGAGTTTTTCCAGATGAGTAAAATCTGGCTTTTCTCAGGTCATTTGGATGTTAAGCGCAATGAGCCGGCACTTACATCTTGAC... | ATCCACCCACCTCAGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACCGCACCCGACCTATTTTGTGGCTTTTGGATATTGTGTCCTAGTTAAAAGGCCTGATCACACTGCAAGATTGTAAAATAATTTCCCCATGATTTCTTTTGGTACTCTTATGTTTTAATTTTTTATATTTAAATCTTTTATCTATTGAGGATTTTTTTCCTGGGGTTCTGTGTGAGTTTGGATCCAATTTGAGTTTTTCCAGATGAGTAAAATCTGGCTTTTCTCAGGTCATTTGGATGTTAAGCGCAATGAGCCGGCACTTACATCTTGAC... |
Task1_train_42537 | A genetic alteration is present on Chromosome 12. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GGGAGGGGACACCTTAGCACAGGGGGTCTACGTGGGTGTCACCCTGGGGGGAGGCAATGGCCTGGGGGGCATCACCAGGACCACAGTTGGCTCGACTGCATGGAAGTGGCCGGGCAAGCTGCAAACCCAGCACGGAGCCCTTCTCCCTGGCCTCTGAGGAGGCTTGTGTGGCCTGGGGATGGGTAGATTGTTCTGGAAGGCCAGTCCTACCACCCTTAGCCCTTGGCTCACAAATTGGTGAGAAAAATTCATTTCCCAATGGCTGTTTCTTCCAGATGGGGATCCCAGGGCCTTCCCCCCGATGAGCTCTCCGTTCAGAA... | GGGAGGGGACACCTTAGCACAGGGGGTCTACGTGGGTGTCACCCTGGGGGGAGGCAATGGCCTGGGGGGCATCACCAGGACCACAGTTGGCTCGACTGCATGGAAGTGGCCGGGCAAGCTGCAAACCCAGCACGGAGCCCTTCTCCCTGGCCTCTGAGGAGGCTTGTGTGGCCTGGGGATGGGTAGATTGTTCTGGAAGGCCAGTCCTACCACCCTTAGCCCTTGGCTCACAAATTGGTGAGAAAAATTCATTTCCCAATGGCTGTTTCTTCCAGATGGGGATCCCAGGGCCTTCCCCCCGATGAGCTCTCCGTTCAGAA... |
Task1_train_42538 | A genomic change on Chromosome 12 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CACTGCTGAGCCTGCCCGAGCGTCAGGGCACTGCAACGCTTCTAAACCTGCGCACTCCCTGGGCCCGCCCAGACTTCTGGGGTCACAGCCCCCAGGGGAGGGAAGCCAAGAGTCTATGCTGTACCCTGGGTCCCGAAACTGCTTGGAATTGGGCAGTTTTGGGTGCACTAATGTAAAACAATGATTTTCACCACTGGGAGGGGAGACGCCCCGACTGGAACCACCTGAGAGGCTTTTGAAACTGCCTCCCCTAAGACACAGCCCTTGCTGTGAGACCCTGCTGCTGCTGGGAGTACTACATCAGGTGGGTGGGTGGGTGG... | CACTGCTGAGCCTGCCCGAGCGTCAGGGCACTGCAACGCTTCTAAACCTGCGCACTCCCTGGGCCCGCCCAGACTTCTGGGGTCACAGCCCCCAGGGGAGGGAAGCCAAGAGTCTATGCTGTACCCTGGGTCCCGAAACTGCTTGGAATTGGGCAGTTTTGGGTGCACTAATGTAAAACAATGATTTTCACCACTGGGAGGGGAGACGCCCCGACTGGAACCACCTGAGAGGCTTTTGAAACTGCCTCCCCTAAGACACAGCCCTTGCTGTGAGACCCTGCTGCTGCTGGGAGTACTACATCAGGTGGGTGGGTGGGTGG... |
Task1_train_42539 | With a mutation on Chromosome 12, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TCCTCAAACACCCATGCATGTTCTCTTTGTATGGAACATATTAAAAGTGTTACTTTAAGAAGACCTATTGATTTCATTTAGTTAATTTTAAAGTATCATAGCGTATAGAGTAAAAGAAATGAAAAGATTGCTAAAACATAGTCCTAAACCTTAAAAGATTTCAGAGTGAATATTTTGAGATTTATTTTCTTCTTTTATCTCCTCCTTATTCTATTTGTGGTGTATTTTGTCCCCTGTAGGCTATCAAAGACTGGAAATAAGGCACTAAGAAATGTACCTTTATCTGCTCCACCAGAATGAAGCAGGATATGTGTGTGGGT... | TCCTCAAACACCCATGCATGTTCTCTTTGTATGGAACATATTAAAAGTGTTACTTTAAGAAGACCTATTGATTTCATTTAGTTAATTTTAAAGTATCATAGCGTATAGAGTAAAAGAAATGAAAAGATTGCTAAAACATAGTCCTAAACCTTAAAAGATTTCAGAGTGAATATTTTGAGATTTATTTTCTTCTTTTATCTCCTCCTTATTCTATTTGTGGTGTATTTTGTCCCCTGTAGGCTATCAAAGACTGGAAATAAGGCACTAAGAAATGTACCTTTATCTGCTCCACCAGAATGAAGCAGGATATGTGTGTGGGT... |
Task1_train_42540 | This variant lies on Chromosome 12. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TCTATTCTTCTACCCCCACACATCTGCCCACCCACCCACCTCCCATATACCTCCCACCAAGCATCCTCTTATCTGCTCATCCTCCTACTGACCACCCATCCACCTGCCCGCCCCCTCCCCCATGCCAACCTGGCCCACCTCAGGACCGTGGGCGTGCTGGGCTCCACAGCGGTGATGATACCCTTCATGCCTGTGTTGTGAAGCACACTGGGTCTCTGCTGGAGGGCATCCTGGGTCCGAGGGGAGATGGGCGAGTGCTGGTGGGCATGGGAGTGGGAGGCGGGGCGGCTGCTGCTGCCCCCACCCCCGCCGCTGCTGCC... | TCTATTCTTCTACCCCCACACATCTGCCCACCCACCCACCTCCCATATACCTCCCACCAAGCATCCTCTTATCTGCTCATCCTCCTACTGACCACCCATCCACCTGCCCGCCCCCTCCCCCATGCCAACCTGGCCCACCTCAGGACCGTGGGCGTGCTGGGCTCCACAGCGGTGATGATACCCTTCATGCCTGTGTTGTGAAGCACACTGGGTCTCTGCTGGAGGGCATCCTGGGTCCGAGGGGAGATGGGCGAGTGCTGGTGGGCATGGGAGTGGGAGGCGGGGCGGCTGCTGCTGCCCCCACCCCCGCCGCTGCTGCC... |
Task1_train_42541 | 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 | CTCTGCCACGGGAAGGTATTCATGGTCTGGGAGTGTGGGTTCTGAGTCCTTCTGTCCTCCCTACATAATTCAGTCTAGAAACTGGAGGGAGTTCCATTTTGCTCGCTGGAGTCACAGCCCTGCTGGGTTCTGGCTCCCCCTGGGGCAGTAACAGAGAAGGGGGCTCCCAAAAGGGCTGGTTGGACCCAATGGTCATTGTTCATCGGGAGCTCAAACGCTAGAGCAGCAACATGATGACAGCTGGTGTCCAGGCTACCATCTCACATTGTGGAAACCTTTTCCCCCCGAGGACAGGAATTTTGAAAGGAAGTCGGGTTTCA... | CTCTGCCACGGGAAGGTATTCATGGTCTGGGAGTGTGGGTTCTGAGTCCTTCTGTCCTCCCTACATAATTCAGTCTAGAAACTGGAGGGAGTTCCATTTTGCTCGCTGGAGTCACAGCCCTGCTGGGTTCTGGCTCCCCCTGGGGCAGTAACAGAGAAGGGGGCTCCCAAAAGGGCTGGTTGGACCCAATGGTCATTGTTCATCGGGAGCTCAAACGCTAGAGCAGCAACATGATGACAGCTGGTGTCCAGGCTACCATCTCACATTGTGGAAACCTTTTCCCCCCGAGGACAGGAATTTTGAAAGGAAGTCGGGTTTCA... |
Task1_train_42542 | A genomic variant on Chromosome 12 is under review. What is the biological outcome — benign or pathogenic? | Benign | GTCTTGGGCTGGGCGTGTCTTCCTGCCTTCACACCACTCGGCCCCAAACCAATCGCCTTTGGGATATCCACAGAAGGATGCTGGGAGGCTCCTGTTCAACTTTAAGCCAGATGCTCCTAGCTCCAGGACAATTGAGGACAATGTGGTTTTCCTCTTTAGAAGCCCAGGAGAGGAGTGGGGAAATTTGGTGGTGCATGCATGTGTGGTGCACACACACACACACACATCCTACTGACATACTTAACCTGATGACATCCTGAGAAAGAAAACACCTTGAAATAAGCCCCCGAATAACTGAGTTGGCAAGACTCTTTACCTGG... | GTCTTGGGCTGGGCGTGTCTTCCTGCCTTCACACCACTCGGCCCCAAACCAATCGCCTTTGGGATATCCACAGAAGGATGCTGGGAGGCTCCTGTTCAACTTTAAGCCAGATGCTCCTAGCTCCAGGACAATTGAGGACAATGTGGTTTTCCTCTTTAGAAGCCCAGGAGAGGAGTGGGGAAATTTGGTGGTGCATGCATGTGTGGTGCACACACACACACACACATCCTACTGACATACTTAACCTGATGACATCCTGAGAAAGAAAACACCTTGAAATAAGCCCCCGAATAACTGAGTTGGCAAGACTCTTTACCTGG... |
Task1_train_42543 | Given this context: Chromosome 12 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TTCTGCCAAGCCAGGGCTGACCGTGCACAAAGCACAAAGCCCCTGCCTCAGTGACCCCATCCTGTCTACTCCCACCCCCTGGCCCTGGTCAAACTCACATTTGGGGTTTTTCTTCCAAGCAGCCAGCAAGGCTTCATGGCAGTCAGCCTTCTCTGCAACCAGGGCTCGCAGAAGGCTCTCCGTACGGGGCTGCAGCCTGTGGGGCAGGAATGCACGTTGGTGGCAGGCAGCCAGGGCACAGACCGGCTGCTGCTGGGGGCCCGAAAGCAGGGCAGGCATCACCACCCCACCAGCCCCACCCAGGAGGGTGAAGAGCTGGC... | TTCTGCCAAGCCAGGGCTGACCGTGCACAAAGCACAAAGCCCCTGCCTCAGTGACCCCATCCTGTCTACTCCCACCCCCTGGCCCTGGTCAAACTCACATTTGGGGTTTTTCTTCCAAGCAGCCAGCAAGGCTTCATGGCAGTCAGCCTTCTCTGCAACCAGGGCTCGCAGAAGGCTCTCCGTACGGGGCTGCAGCCTGTGGGGCAGGAATGCACGTTGGTGGCAGGCAGCCAGGGCACAGACCGGCTGCTGCTGGGGGCCCGAAAGCAGGGCAGGCATCACCACCCCACCAGCCCCACCCAGGAGGGTGAAGAGCTGGC... |
Task1_train_42544 | Given this context: Chromosome 12 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AGTTCGCACCACTATACTCTAATCTGGGCAACAGAGTGAGGCTCTGTCTCAAAAAAGAAAACAACAACAACAAAATTAGTCGGAGGTGGTGGTGTGCCCCCTGCAGTCCCAACTACTCAGGAGGCTGTGGCGAGAAGGTTATTTGTGCCTGGGAATTCGAGGCTGCAGTGAGCTATGATTGTGCCACTGCACTCTATCCTGGGCAACAGAGCGAGACCTTGTTTCTAGAAAACACAAAAAACCCCAAAAGAGTTTAAATGCTGTGTGAATTTTATCTCCACTAAACTGTTATTAAAAAAAAAAAGTTGGGAGAAACTAAC... | AGTTCGCACCACTATACTCTAATCTGGGCAACAGAGTGAGGCTCTGTCTCAAAAAAGAAAACAACAACAACAAAATTAGTCGGAGGTGGTGGTGTGCCCCCTGCAGTCCCAACTACTCAGGAGGCTGTGGCGAGAAGGTTATTTGTGCCTGGGAATTCGAGGCTGCAGTGAGCTATGATTGTGCCACTGCACTCTATCCTGGGCAACAGAGCGAGACCTTGTTTCTAGAAAACACAAAAAACCCCAAAAGAGTTTAAATGCTGTGTGAATTTTATCTCCACTAAACTGTTATTAAAAAAAAAAAGTTGGGAGAAACTAAC... |
Task1_train_42545 | This sequence variant lies on Chromosome 12. Is it clinically significant, and what condition might it cause if any? | Benign | CTGGATTAATCTAAAAAATTTTTTGTAGAGACATGGTCTCACCATGTTGCCCAAGCTGGTCTCAAACTCTAGGCCTCAAGCGATCCTCCCACCTTGGCCTCCCAAAGTGCTGGAATTACAGGCATGAGCCACTGTGCCTGACCAGGAACTGGATTTTTAACTTCATTTTATTCCAATTACACTTAAACCTAAGCAGCCACATGGGGCTGGTAGCTGCCATCCTGGACAACGCAGCCTTACTCTCCAGGAGTCCCTGCCAGCCCCCCACGTACCTCAGCCCGCGCCTTCTTGGCCCTGGCCCTTGACTTCTTAAACTTCCG... | CTGGATTAATCTAAAAAATTTTTTGTAGAGACATGGTCTCACCATGTTGCCCAAGCTGGTCTCAAACTCTAGGCCTCAAGCGATCCTCCCACCTTGGCCTCCCAAAGTGCTGGAATTACAGGCATGAGCCACTGTGCCTGACCAGGAACTGGATTTTTAACTTCATTTTATTCCAATTACACTTAAACCTAAGCAGCCACATGGGGCTGGTAGCTGCCATCCTGGACAACGCAGCCTTACTCTCCAGGAGTCCCTGCCAGCCCCCCACGTACCTCAGCCCGCGCCTTCTTGGCCCTGGCCCTTGACTTCTTAAACTTCCG... |
Task1_train_42546 | Given a variant located on Chromosome 12, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CAGCTGGAGGAGGAGGAACAGTCATCCCAGCCGGCACGGGCTGACTGCTGGGTGCTGGAGCTGGCGGCAGAGGTGCCACGGTGGTCCCCACACCAGCCTCAGCCGGCTCAGCAGCTGGGTCCTCGTCCAGCTCCGACTCCTCCTCCAGCTCCGATTCCGACTCCTCCTCCTCCTCCTCCTCCTCCTCAGCTGAGGGCCAGCGGCGACGCTTCCGGTGGGCACCGCTGAGGCTACTGATCTTCTCCTGGCCCGGGGCTACCACCTCGTCAGCCTTCCTGTTGAGATAGCAGAGACTTCAGGCACAGAGGCCCCACCTCAAT... | CAGCTGGAGGAGGAGGAACAGTCATCCCAGCCGGCACGGGCTGACTGCTGGGTGCTGGAGCTGGCGGCAGAGGTGCCACGGTGGTCCCCACACCAGCCTCAGCCGGCTCAGCAGCTGGGTCCTCGTCCAGCTCCGACTCCTCCTCCAGCTCCGATTCCGACTCCTCCTCCTCCTCCTCCTCCTCCTCAGCTGAGGGCCAGCGGCGACGCTTCCGGTGGGCACCGCTGAGGCTACTGATCTTCTCCTGGCCCGGGGCTACCACCTCGTCAGCCTTCCTGTTGAGATAGCAGAGACTTCAGGCACAGAGGCCCCACCTCAAT... |
Task1_train_42547 | Here’s a variant located on Chromosome 12. What is the predicted biological effect — harmless or disease-causing? | Benign | GTTTAATTATGTTAAAATACATATATCATAAACTATTATGTAACCATCTTAACTATTTTAAACTGTACACTTCAGTGATGTTAAGTACATTTACATTGTTGTAGTTTTTTTTTTTTTTTTTTTTTGAGGTGGAGTCTTGCTCTATTGCCCAGGCTGGAGTGCAGTGGGGCCATCTTAGTATACTGCAACCTCCACCTCCCAGGTTCTAGCAGTTCTCCTGCCTCAGCCTCCTGAGTAACTGGGATTACAGTCATGCACCACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGTTGCCCAGGC... | GTTTAATTATGTTAAAATACATATATCATAAACTATTATGTAACCATCTTAACTATTTTAAACTGTACACTTCAGTGATGTTAAGTACATTTACATTGTTGTAGTTTTTTTTTTTTTTTTTTTTTGAGGTGGAGTCTTGCTCTATTGCCCAGGCTGGAGTGCAGTGGGGCCATCTTAGTATACTGCAACCTCCACCTCCCAGGTTCTAGCAGTTCTCCTGCCTCAGCCTCCTGAGTAACTGGGATTACAGTCATGCACCACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGTTGCCCAGGC... |
Task1_train_42548 | This is a variant located on Chromosome 12. Is this mutation a likely cause of disease or not? | Benign | TTTCAGTTTCTAGCTTTTAGGCCAGTTCAGAGTTCAGTCCATAAAATGATTTAAAAATGCTCTGGGCCAATGAGTGAGCTGGCTTCCTGGGAAGAAGAACCACTTTTGCTGATTTGTGACATAGTCTCATGTTTTGCTGATCTGTAGCGTAGTCTCATGTGTGTGCGTCTTGGTTTGTTGTCATTCTCTATAGGTTGTGGACACATCGAAAGGAATCGCAGATGTCCCCGAGTGGTTCAAAGGCAGTCGGCTCAACTATGCAGAAAACCTCCTGCGGCACAAAGAGAATGACAGAGTTGCCCTTTACATTGCAAGTAAGT... | TTTCAGTTTCTAGCTTTTAGGCCAGTTCAGAGTTCAGTCCATAAAATGATTTAAAAATGCTCTGGGCCAATGAGTGAGCTGGCTTCCTGGGAAGAAGAACCACTTTTGCTGATTTGTGACATAGTCTCATGTTTTGCTGATCTGTAGCGTAGTCTCATGTGTGTGCGTCTTGGTTTGTTGTCATTCTCTATAGGTTGTGGACACATCGAAAGGAATCGCAGATGTCCCCGAGTGGTTCAAAGGCAGTCGGCTCAACTATGCAGAAAACCTCCTGCGGCACAAAGAGAATGACAGAGTTGCCCTTTACATTGCAAGTAAGT... |
Task1_train_42549 | A sequence alteration has been identified on Chromosome 12. Is it disease-inducing or harmless? | Benign | AGTGGAATGGACTCCTGGCATTTGAGGGCTTCCCGACTGCAGCCCTCAGGCAGCCATGGCTGTCCCAAGTCCAGCGGGCCTTTGCTCGGGTCATGGCTGGGATGTCTGGCCCTTCCTGACAGGAGGCTGCTGGGCTCCTGTCTACTTGGGGACGCCTCATGCAGGAGCTGGTGTGGGGGTGGGCAGGGGGGCGGTGGCTTCTTCCTTTCTCTTTCCCTTTCCTCTACCTTTTCCCCTCTCCCCAGAGGAAATGGTAGCAGGATTTCTTTTAAGAGGATGCTGCTGTATTTTGCCAGCGGGTGGAAGGTGGCGGTATTAGC... | AGTGGAATGGACTCCTGGCATTTGAGGGCTTCCCGACTGCAGCCCTCAGGCAGCCATGGCTGTCCCAAGTCCAGCGGGCCTTTGCTCGGGTCATGGCTGGGATGTCTGGCCCTTCCTGACAGGAGGCTGCTGGGCTCCTGTCTACTTGGGGACGCCTCATGCAGGAGCTGGTGTGGGGGTGGGCAGGGGGGCGGTGGCTTCTTCCTTTCTCTTTCCCTTTCCTCTACCTTTTCCCCTCTCCCCAGAGGAAATGGTAGCAGGATTTCTTTTAAGAGGATGCTGCTGTATTTTGCCAGCGGGTGGAAGGTGGCGGTATTAGC... |
Task1_train_42550 | This variant is present on Chromosome 12. Is the change likely to result in a pathogenic outcome? | Benign | TGCCATTCTTGTTGCAAGCAGAAAGCACATCATCCTCATCAAAGTGTGCTTGTGGAATGAGTGAATGAACTGGGAGTGGATAGATGGCTGAGCAGGTCCTGCAGGAGAAGGACCATTTCATTTCATTCTGTGGGCTCACCTAGAATCTGAAAAACAAGGGCATGCAGAACTTCTTAACAATGAAGACTTTGTTCTGTTTCGATTCCTTGTGCTCCAGGCCTACCCGGGAAAGCGATGACGAGGACGATGAGGAGAAGAAGGGACGAGGCTGCTCCCTGCAGTACCAGCACGCCACAGTGCGTGTCCTCACCCAGTTTGTG... | TGCCATTCTTGTTGCAAGCAGAAAGCACATCATCCTCATCAAAGTGTGCTTGTGGAATGAGTGAATGAACTGGGAGTGGATAGATGGCTGAGCAGGTCCTGCAGGAGAAGGACCATTTCATTTCATTCTGTGGGCTCACCTAGAATCTGAAAAACAAGGGCATGCAGAACTTCTTAACAATGAAGACTTTGTTCTGTTTCGATTCCTTGTGCTCCAGGCCTACCCGGGAAAGCGATGACGAGGACGATGAGGAGAAGAAGGGACGAGGCTGCTCCCTGCAGTACCAGCACGCCACAGTGCGTGTCCTCACCCAGTTTGTG... |
Task1_train_42551 | A variant was discovered on Chromosome 12. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CCAATACAATATGACTGATTCATATGACATTACTGTTACTGACTTCACTTATCCAAAAACTATAATCACCCAATGTATTGTTAATATTGTTACTTTAACAGTTACCATTTAGTCCAATTACAAGAAAGAACAATAGTTTTATCTTTTTCTGATGATCTTTTTTTCCTTATGGAGATCTGAGTTTTTGACACTATTGCATTACTGTCACAAGACAAAATTACACTTCCACTTCATGAGCAATGCTTTTGTTCTAGATGTAACTTCTTGCCACCTTCATTACACAGAAGAGATATCTGCTTGCAAAACTTTACAGTTCAGAG... | CCAATACAATATGACTGATTCATATGACATTACTGTTACTGACTTCACTTATCCAAAAACTATAATCACCCAATGTATTGTTAATATTGTTACTTTAACAGTTACCATTTAGTCCAATTACAAGAAAGAACAATAGTTTTATCTTTTTCTGATGATCTTTTTTTCCTTATGGAGATCTGAGTTTTTGACACTATTGCATTACTGTCACAAGACAAAATTACACTTCCACTTCATGAGCAATGCTTTTGTTCTAGATGTAACTTCTTGCCACCTTCATTACACAGAAGAGATATCTGCTTGCAAAACTTTACAGTTCAGAG... |
Task1_train_42552 | Chromosome 12 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | AGTCAAAGAAAAGTGCAAATGTAATGCCAAGTTCCCTTCCAGAAAGGTCGTACCGCTTTTCATTCTCAGCAGCAATATACTAAGACTGTCTATTGCCTGTCGACTTCCCAACATTGTGTGTTATACTTGGTAATTTTTGTCAGTCTTATAGGTAAGAGGTGGTATTTGTAGTTTTCATCTGTGTTTCTCTAATTGTGAGTGAGGCTCAATAGTTGTAAATATATATATATAAATAATTTTAATATATTTTTGTGAATATCTGTTCATATCCTTTACTCACTTCTCTCTCAATTTTTAAAAATCTTTTTCCTCAAATTTCA... | AGTCAAAGAAAAGTGCAAATGTAATGCCAAGTTCCCTTCCAGAAAGGTCGTACCGCTTTTCATTCTCAGCAGCAATATACTAAGACTGTCTATTGCCTGTCGACTTCCCAACATTGTGTGTTATACTTGGTAATTTTTGTCAGTCTTATAGGTAAGAGGTGGTATTTGTAGTTTTCATCTGTGTTTCTCTAATTGTGAGTGAGGCTCAATAGTTGTAAATATATATATATAAATAATTTTAATATATTTTTGTGAATATCTGTTCATATCCTTTACTCACTTCTCTCTCAATTTTTAAAAATCTTTTTCCTCAAATTTCA... |
Task1_train_42553 | This variant is found on Chromosome 12. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CTAAAGTATTCTTAGCCTCCATAATAGACATTGTGCAAGCTGCCTGGATTGCAGCCCAGCTCCAGGAATCCCACGGACCCAGGAGAAGACACAGCCGAGGGTGGTAACTGCTGGCTGATGCAAAAGCATCACAGAGAGGCCGAGGCTCTACTTAAAACTCATAACTCTTTTAGCTGCGCCCTTGTTTAATGCAAAAGGTCATTTTTGTGTCAATTGCTTCCCTGGAGAAAGAACGGAGAAAATCTTTTTCCACCTCCTGCTTCACACCAGAGCAGTGTTTCTGGAAAGGGACTTTGTGAGAAACTGGCATCATTAGATGT... | CTAAAGTATTCTTAGCCTCCATAATAGACATTGTGCAAGCTGCCTGGATTGCAGCCCAGCTCCAGGAATCCCACGGACCCAGGAGAAGACACAGCCGAGGGTGGTAACTGCTGGCTGATGCAAAAGCATCACAGAGAGGCCGAGGCTCTACTTAAAACTCATAACTCTTTTAGCTGCGCCCTTGTTTAATGCAAAAGGTCATTTTTGTGTCAATTGCTTCCCTGGAGAAAGAACGGAGAAAATCTTTTTCCACCTCCTGCTTCACACCAGAGCAGTGTTTCTGGAAAGGGACTTTGTGAGAAACTGGCATCATTAGATGT... |
Task1_train_42554 | Consider a variant on Chromosome 12. Determine its clinical classification and disease relevance. | Benign | TCCATGTGTTCTCATCATTTAGCTCCCACTTAGAAGTGAGAACATGTAGTGTTGGGTTTTCTGTTTCTGTGTCAGTTTGCTAAGAATAATGGCCTCTAGCTCCATCTGGTCCCTGCAAAGGATGGGATCTTGTTCTTTTTATGGCTGCATAGTATTCCACGGTGTGTGTGTACCACATTTTCTTTATCCAGTTTATCATTAATGGTCTGGAGAGTTTTTCCTAGATGAATGGAGGAGGCTGAAATATGCAATTCTAAGCACAAAGTGGAGAGCCTGTATCCACTGGGCACTTGCTGTGGATCAGGTGCCATTTAGGTTGA... | TCCATGTGTTCTCATCATTTAGCTCCCACTTAGAAGTGAGAACATGTAGTGTTGGGTTTTCTGTTTCTGTGTCAGTTTGCTAAGAATAATGGCCTCTAGCTCCATCTGGTCCCTGCAAAGGATGGGATCTTGTTCTTTTTATGGCTGCATAGTATTCCACGGTGTGTGTGTACCACATTTTCTTTATCCAGTTTATCATTAATGGTCTGGAGAGTTTTTCCTAGATGAATGGAGGAGGCTGAAATATGCAATTCTAAGCACAAAGTGGAGAGCCTGTATCCACTGGGCACTTGCTGTGGATCAGGTGCCATTTAGGTTGA... |
Task1_train_42555 | This sequence change occurs on Chromosome 12. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CTCAGACCATCAACTTTTCTGCAAGCTAGCCCCTGCTTTTTTTTCCCTTATTTTTGCCCAAGAAGACTTTCAAAGACTATCCTAAGAGGAAATCGGCTTCCTAAGTAAAAGTAACTCCAAACCCTCTCCACACTGCCATTTGTGCTTTAAAACCCAAATATGTCCACAGAACAATGCTGTTCTCTTGCAGAAATGTCTATGGGCTACCACCCACACGGATACTAAAACTTTAAGGGTTGTTCCTGAAAAAGACCTCTAGGATCCGAAACACTGCTTTTGTCTGATCAAATAAGGCCCTGGCAAAAGACTAGTGTCAGCTA... | CTCAGACCATCAACTTTTCTGCAAGCTAGCCCCTGCTTTTTTTTCCCTTATTTTTGCCCAAGAAGACTTTCAAAGACTATCCTAAGAGGAAATCGGCTTCCTAAGTAAAAGTAACTCCAAACCCTCTCCACACTGCCATTTGTGCTTTAAAACCCAAATATGTCCACAGAACAATGCTGTTCTCTTGCAGAAATGTCTATGGGCTACCACCCACACGGATACTAAAACTTTAAGGGTTGTTCCTGAAAAAGACCTCTAGGATCCGAAACACTGCTTTTGTCTGATCAAATAAGGCCCTGGCAAAAGACTAGTGTCAGCTA... |
Task1_train_42556 | A variant on Chromosome 12 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GTTCAACTCTCCTTAGGGAGGTTCCTTTCTGGGCTCATGCTGAAGTCGCCTTTGTAAAATCAGAAATGTATCTGTTCACATTTAGCTTTTAATATCCCATGGGCAAGGTGAAATAGGGGAAGATCATGGGCAAGTGCCCCCCTCTACTTCTGTATACCACACCAGACACTGCGTTTTATTGCCTCTTCTTGGTGTGTAGCAAATATATCAGGAGTCCACTCAAAACTTATTTATTTATTTAACACTGAGTCTTGCTTTACTGCCTAGGCTGGAGCGCAGTGGCATGATCGCGGCTCACTGCAACCTCCGCCTCCTGGGTT... | GTTCAACTCTCCTTAGGGAGGTTCCTTTCTGGGCTCATGCTGAAGTCGCCTTTGTAAAATCAGAAATGTATCTGTTCACATTTAGCTTTTAATATCCCATGGGCAAGGTGAAATAGGGGAAGATCATGGGCAAGTGCCCCCCTCTACTTCTGTATACCACACCAGACACTGCGTTTTATTGCCTCTTCTTGGTGTGTAGCAAATATATCAGGAGTCCACTCAAAACTTATTTATTTATTTAACACTGAGTCTTGCTTTACTGCCTAGGCTGGAGCGCAGTGGCATGATCGCGGCTCACTGCAACCTCCGCCTCCTGGGTT... |
Task1_train_42557 | A mutation on Chromosome 12 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TAGGGAGGTTCCTTTCTGGGCTCATGCTGAAGTCGCCTTTGTAAAATCAGAAATGTATCTGTTCACATTTAGCTTTTAATATCCCATGGGCAAGGTGAAATAGGGGAAGATCATGGGCAAGTGCCCCCCTCTACTTCTGTATACCACACCAGACACTGCGTTTTATTGCCTCTTCTTGGTGTGTAGCAAATATATCAGGAGTCCACTCAAAACTTATTTATTTATTTAACACTGAGTCTTGCTTTACTGCCTAGGCTGGAGCGCAGTGGCATGATCGCGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAATGATTCTCA... | TAGGGAGGTTCCTTTCTGGGCTCATGCTGAAGTCGCCTTTGTAAAATCAGAAATGTATCTGTTCACATTTAGCTTTTAATATCCCATGGGCAAGGTGAAATAGGGGAAGATCATGGGCAAGTGCCCCCCTCTACTTCTGTATACCACACCAGACACTGCGTTTTATTGCCTCTTCTTGGTGTGTAGCAAATATATCAGGAGTCCACTCAAAACTTATTTATTTATTTAACACTGAGTCTTGCTTTACTGCCTAGGCTGGAGCGCAGTGGCATGATCGCGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAATGATTCTCA... |
Task1_train_42558 | This genomic variant is located on Chromosome 12. Can you determine its pathogenicity and name any linked disease? | Benign | TTGATTCTCTGGCCTCCCTCTTCCACTTGTAACGACCCCTGTGGTTATGTTGAGCCTGCCTCGATAGTCTACCGTAATACCCCTCCCCTGTCCCAGCCTCATGGGTCCTGGGAATTAGGATGTGGACATCTCTGGGAGCAATTATTCTCCCTACCACAGATTCATGTCCTTACCATATGAGAAAAATCTTCACTCTGTCTCAACATCTCCCAAAGCCTAAACCCCTGGTGAACCACCTCTACTGGGCGGGCGTTTCTATGTCTCTCTGTGTTTTTGGAAAAGTTCTTACAGGTCTGTAGTAAGAAATTCAAACAATATAA... | TTGATTCTCTGGCCTCCCTCTTCCACTTGTAACGACCCCTGTGGTTATGTTGAGCCTGCCTCGATAGTCTACCGTAATACCCCTCCCCTGTCCCAGCCTCATGGGTCCTGGGAATTAGGATGTGGACATCTCTGGGAGCAATTATTCTCCCTACCACAGATTCATGTCCTTACCATATGAGAAAAATCTTCACTCTGTCTCAACATCTCCCAAAGCCTAAACCCCTGGTGAACCACCTCTACTGGGCGGGCGTTTCTATGTCTCTCTGTGTTTTTGGAAAAGTTCTTACAGGTCTGTAGTAAGAAATTCAAACAATATAA... |
Task1_train_42559 | Here’s a variant located on Chromosome 12. What is the predicted biological effect — harmless or disease-causing? | Benign | TCTTAAGCAATGCTGAACCTTTCGGGGCTGACTGCAGGACCAAGTGCTTGCAAACCTGCATCTTCACCACATGCACTGATGCCCCTTATCCCTTCGCACCTCCAAGATGAAGAAGGTTTCTGTGCTGTCCGGTGTGTGTGAGGCTGGGCTTCCTGCTGGATCCACCACTTTCACACCCAGAACCCCCCCAACTCCACACGCCCTGCACGTTCCACACAGGCACCCCGATTTGTCTCAACAGCCTCGAGGCCACATCTTTGGACAGGAGATCTGCCATGAACAGTGAAAGACCCATCCCAAGTGGCCCTGTTTTCTTTCTA... | TCTTAAGCAATGCTGAACCTTTCGGGGCTGACTGCAGGACCAAGTGCTTGCAAACCTGCATCTTCACCACATGCACTGATGCCCCTTATCCCTTCGCACCTCCAAGATGAAGAAGGTTTCTGTGCTGTCCGGTGTGTGTGAGGCTGGGCTTCCTGCTGGATCCACCACTTTCACACCCAGAACCCCCCCAACTCCACACGCCCTGCACGTTCCACACAGGCACCCCGATTTGTCTCAACAGCCTCGAGGCCACATCTTTGGACAGGAGATCTGCCATGAACAGTGAAAGACCCATCCCAAGTGGCCCTGTTTTCTTTCTA... |
Task1_train_42560 | With a mutation on Chromosome 12, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GTATATCCCCTGGTATGGAATTCACCGTGACTACCGCCCATGCCTAGAGACCAGCCTCTTCAAAGACGGACGGCGTGGGACATATGCCCAGGTTGCGGGGGGAGCTTCTCTACAGAATGTCACTTGGGAGTTGACACAAAACCCAGGGGGAGAAAAAAGACCCAGCAAATACTACAAACTGCCCTCTCCCTCCCCCACCCACAGGTGACCAACGGCTTTGGGGAGGATGGCAATGCAGTGGAGGAATAGAAATGGATACATTGTGAACTTGATATGAATCAAAAGAGCGTGGTTCTTTGAACCTGATTCAAATTCTATGC... | GTATATCCCCTGGTATGGAATTCACCGTGACTACCGCCCATGCCTAGAGACCAGCCTCTTCAAAGACGGACGGCGTGGGACATATGCCCAGGTTGCGGGGGGAGCTTCTCTACAGAATGTCACTTGGGAGTTGACACAAAACCCAGGGGGAGAAAAAAGACCCAGCAAATACTACAAACTGCCCTCTCCCTCCCCCACCCACAGGTGACCAACGGCTTTGGGGAGGATGGCAATGCAGTGGAGGAATAGAAATGGATACATTGTGAACTTGATATGAATCAAAAGAGCGTGGTTCTTTGAACCTGATTCAAATTCTATGC... |
Task1_train_42561 | A mutation is present on Chromosome 12. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GTGCTGTTTTTTTAAGGGTCAACCCAGGACGCTACGGGAAGCACCTGGCGCATCCTTGGGAACAGTGGGGCTTGGCGGTGGGCGCCCACCGCGAACGCCCTGGGCGGGGGAAGGGAATGGCGGGGGGACGTCGTGTCCTAAGTGACCCCGTCACAGACCCGCCCCAATCCGAGGGGGGATGAGCTCAGAGGACCTGCCCAGGACGCTCCTTCTCCACTTTCCAGGAAAACCGAGCGGCGTGCGCGCCTCCGTGTCCTCGCGGGAGCTGGGGGTCCCCGGGCAGGCGCTGACGCGCTCCTCCCACGACCCACTCCATCCCA... | GTGCTGTTTTTTTAAGGGTCAACCCAGGACGCTACGGGAAGCACCTGGCGCATCCTTGGGAACAGTGGGGCTTGGCGGTGGGCGCCCACCGCGAACGCCCTGGGCGGGGGAAGGGAATGGCGGGGGGACGTCGTGTCCTAAGTGACCCCGTCACAGACCCGCCCCAATCCGAGGGGGGATGAGCTCAGAGGACCTGCCCAGGACGCTCCTTCTCCACTTTCCAGGAAAACCGAGCGGCGTGCGCGCCTCCGTGTCCTCGCGGGAGCTGGGGGTCCCCGGGCAGGCGCTGACGCGCTCCTCCCACGACCCACTCCATCCCA... |
Task1_train_42562 | Chromosome 12 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TGTTTAGTATTTTATGTGGCTTTGAGGGGTATCTTTTGAGGGAGTGGCAGAAAGTAACTTTCTCCTTTGGTATCTGTAGTATTTGGGGTGGGCTTGTTCTTCGTGTTTCTAAGCAAGGCTACCTATACCTCACTTATTCCTCAGGAAATAATGAAGTTAAACTTTGCAGTGCGTAGTCTTTCTAACTCTTCCATTAGCAAAAGGTGACAACAGAAAAAGGGGATGTTTCTGGTCAAATCTTTTTTCTATCTTTGTTATATCAAGGGGTTTCCTTTGACGGGGAGAAAGTTTGGGCATCAGAATTTTAAGTTAAAGAATGT... | TGTTTAGTATTTTATGTGGCTTTGAGGGGTATCTTTTGAGGGAGTGGCAGAAAGTAACTTTCTCCTTTGGTATCTGTAGTATTTGGGGTGGGCTTGTTCTTCGTGTTTCTAAGCAAGGCTACCTATACCTCACTTATTCCTCAGGAAATAATGAAGTTAAACTTTGCAGTGCGTAGTCTTTCTAACTCTTCCATTAGCAAAAGGTGACAACAGAAAAAGGGGATGTTTCTGGTCAAATCTTTTTTCTATCTTTGTTATATCAAGGGGTTTCCTTTGACGGGGAGAAAGTTTGGGCATCAGAATTTTAAGTTAAAGAATGT... |
Task1_train_42563 | This variant is present on Chromosome 12. Is the change likely to result in a pathogenic outcome? | Benign | AATAAATGTGTGAAACACTAAACAAAGCTAAACAGGCTTCCTTCTAGGAAGCCTTCTCAGAGCCTTGATTATTCTACGGGTACTGCAACTTCCCAAGAGGGGCTGGGCGACGGCACGAAGAGGTCCCCGGAAAGATCTGGCCGCAGGCAGCACCCTGGCTGCACGGACTAGCTCATGAGACGGCGGCTCCAGAAACATTTTGGGAAACACACTTCTGAGTCACTGAGAGGGCATAAACAGAGGCTCAGAATATTATTTTACAAGATACATAAAATTTTAAAATGCACTTTTTCAATTTAATACTACTTTCTTATTTTTTC... | AATAAATGTGTGAAACACTAAACAAAGCTAAACAGGCTTCCTTCTAGGAAGCCTTCTCAGAGCCTTGATTATTCTACGGGTACTGCAACTTCCCAAGAGGGGCTGGGCGACGGCACGAAGAGGTCCCCGGAAAGATCTGGCCGCAGGCAGCACCCTGGCTGCACGGACTAGCTCATGAGACGGCGGCTCCAGAAACATTTTGGGAAACACACTTCTGAGTCACTGAGAGGGCATAAACAGAGGCTCAGAATATTATTTTACAAGATACATAAAATTTTAAAATGCACTTTTTCAATTTAATACTACTTTCTTATTTTTTC... |
Task1_train_42564 | This alteration occurs on Chromosome 12. Is it associated with a disease or is it a benign variant? | Benign | CAAGAATTTCCCCCAAAAGAATCCTTTAACCAAAAAGTTGTGGTTTCTTGCCTTGCTAACTGTACCATAGTTATTCCTGCAGGTGAATATATAGGCTTTATCTGGGTTATTTATTTATTTAATTTTTTTTTGAGACAGGGTTTCGCTCTGTTGCCCAACCTGGAGTGCAGCTTCCGCCTCCTAAGCTCAAGCCATCCTCTTACCTCAGCATCCTGAGTAGCTTGGACTATAGGCACGTGCCACTATGCCTGACTAATTTTTGTATTTTTTTGTAGAGATGGGGATTCACCATGTTGCCCATGCTGGTCTGGAACTCATGA... | CAAGAATTTCCCCCAAAAGAATCCTTTAACCAAAAAGTTGTGGTTTCTTGCCTTGCTAACTGTACCATAGTTATTCCTGCAGGTGAATATATAGGCTTTATCTGGGTTATTTATTTATTTAATTTTTTTTTGAGACAGGGTTTCGCTCTGTTGCCCAACCTGGAGTGCAGCTTCCGCCTCCTAAGCTCAAGCCATCCTCTTACCTCAGCATCCTGAGTAGCTTGGACTATAGGCACGTGCCACTATGCCTGACTAATTTTTGTATTTTTTTGTAGAGATGGGGATTCACCATGTTGCCCATGCTGGTCTGGAACTCATGA... |
Task1_train_42565 | A mutation located on Chromosome 12 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CTGCTCCCTGCCAGACCTCCCTGTCCTGACCCAGGCTCGCAGGAGACGCCAGGCTCCAGCCCCCACCAAGTGGAACAAGAGGAACCTGTCGTGGAGGTGGGTGTGTGGCCAGGGTGAGGAGCGGGGCCTCCGTGGAGGTGGGCGCGTGGCCAGGGTGAGGAACGGGGTCTCCGTGGAGGTGGGCGCGTGGCCAGGGTGGGGAACGGGGTCTCCGTGGAGGCGGGTGCGTGGCCAGGGTGAGGAACAGGGTCTCCGTGGAGGTGGGCGCGTGGCCAGGGTGGGGAACGGGGTCTCCGTGGAGGCGGGTGCGTGGCCAGGGT... | CTGCTCCCTGCCAGACCTCCCTGTCCTGACCCAGGCTCGCAGGAGACGCCAGGCTCCAGCCCCCACCAAGTGGAACAAGAGGAACCTGTCGTGGAGGTGGGTGTGTGGCCAGGGTGAGGAGCGGGGCCTCCGTGGAGGTGGGCGCGTGGCCAGGGTGAGGAACGGGGTCTCCGTGGAGGTGGGCGCGTGGCCAGGGTGGGGAACGGGGTCTCCGTGGAGGCGGGTGCGTGGCCAGGGTGAGGAACAGGGTCTCCGTGGAGGTGGGCGCGTGGCCAGGGTGGGGAACGGGGTCTCCGTGGAGGCGGGTGCGTGGCCAGGGT... |
Task1_train_42566 | This sequence variant lies on Chromosome 12. Is it clinically significant, and what condition might it cause if any? | Benign | TGGGAGGCCAAGGCGGGCGGATCATTTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAGACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGTATGGTGATGTGTGCCTGTAATCCCTGCTATTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCGGAGGCTGCAGTAAGCCAAGATTGTGCCATGGCACTCCAGCCTGGGAAACATAGTGAGACTCTGTCTGAAAAAAAATAAAAATAAAATAGTAAAGACAGGGTTTTGCCATGTTGACCAGGCTGGTCTTGAACTCTTGAGCTCGAG... | TGGGAGGCCAAGGCGGGCGGATCATTTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAGACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGTATGGTGATGTGTGCCTGTAATCCCTGCTATTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCGGAGGCTGCAGTAAGCCAAGATTGTGCCATGGCACTCCAGCCTGGGAAACATAGTGAGACTCTGTCTGAAAAAAAATAAAAATAAAATAGTAAAGACAGGGTTTTGCCATGTTGACCAGGCTGGTCTTGAACTCTTGAGCTCGAG... |
Task1_train_42567 | Given this variant on Chromosome 12, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CATTTCCCAGAGGACCATGAACGTGTGCGTCTTGCGGTCAGTCAGCCCAGCGTCTGTGAGACGGTGCCTGCTTGCATGGTGCAGTCCAGAGTGTATTTTGCAAACGTCTAGCACTGCCTTTATGTAGGACGCGTGCTTCGTTTTATTGGTCTAAAATTTCCCATGTCATAACACTTTGATCATGCCTTAGAGAAGTCTTACAGCTTATTCAGAGCACTTTGGAGACATTAACACCCAGCGTGCAAATGCGTCTTCTTGCTTAGGCGTCTTGTGCCTTGTGTTCAGCATCAGTCTCTAGGCCCGCTTGGTGTGGTTCTGGA... | CATTTCCCAGAGGACCATGAACGTGTGCGTCTTGCGGTCAGTCAGCCCAGCGTCTGTGAGACGGTGCCTGCTTGCATGGTGCAGTCCAGAGTGTATTTTGCAAACGTCTAGCACTGCCTTTATGTAGGACGCGTGCTTCGTTTTATTGGTCTAAAATTTCCCATGTCATAACACTTTGATCATGCCTTAGAGAAGTCTTACAGCTTATTCAGAGCACTTTGGAGACATTAACACCCAGCGTGCAAATGCGTCTTCTTGCTTAGGCGTCTTGTGCCTTGTGTTCAGCATCAGTCTCTAGGCCCGCTTGGTGTGGTTCTGGA... |
Task1_train_42568 | This variant is found on Chromosome 12. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GCTGCATCTTTGTTTCCCAGCAGTTCCACAGGGGGCGCTCAGGGCACTTATCTTAGTGAATTTTATTTATAATTGTTTAAGTGACAGTAAACTAGTAAATGCCTTCTGATTGATTTTAATTTTAGTAAGGACTAACATTTATTTCGACCTTTGTTCATGTGTGAGTAAATCATGTAATTTCACATATTTCGCAGAATAATCTTGGGAAATATTATTTTCATCCGTTTTCTGTAAGTAACAGGACCCAGCAAGAGACCAGGGTCCGTGAGGGCCTTGTGCAGGGAGGGCCCTTGAAATCAGGGCCCCCAGCAGCTGCCCAC... | GCTGCATCTTTGTTTCCCAGCAGTTCCACAGGGGGCGCTCAGGGCACTTATCTTAGTGAATTTTATTTATAATTGTTTAAGTGACAGTAAACTAGTAAATGCCTTCTGATTGATTTTAATTTTAGTAAGGACTAACATTTATTTCGACCTTTGTTCATGTGTGAGTAAATCATGTAATTTCACATATTTCGCAGAATAATCTTGGGAAATATTATTTTCATCCGTTTTCTGTAAGTAACAGGACCCAGCAAGAGACCAGGGTCCGTGAGGGCCTTGTGCAGGGAGGGCCCTTGAAATCAGGGCCCCCAGCAGCTGCCCAC... |
Task1_train_42569 | This variant is found on Chromosome 12. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GCGCCCTCCGGCCCCGCCGCAGCTGCCGCATCGGGGCCCGGGTACCGCGCGACGTAGAACAGCGCCATGGCCAGCCGCACGCCTGGGACTCGGGCGTGGCGCGCTGCGATGACGTCGGCGGCACGCCTGCGACTCGGGCTCCGCGCAAAAGATGGGGTTGGGGTACGGCGCGTAGAGATGACGTCGGGTTCTACGCGCAGTGGTGACGTCACGGGAGCGCCGGCGGCTGAGAATCCGCGTTGTTCCGTGTTGGGGGCGGCATGGAGCGGGAGCCGGGCGCCGCGGGAGTTCGCCGGGCTCTGGGCCGCCGGCTGGAGGCG... | GCGCCCTCCGGCCCCGCCGCAGCTGCCGCATCGGGGCCCGGGTACCGCGCGACGTAGAACAGCGCCATGGCCAGCCGCACGCCTGGGACTCGGGCGTGGCGCGCTGCGATGACGTCGGCGGCACGCCTGCGACTCGGGCTCCGCGCAAAAGATGGGGTTGGGGTACGGCGCGTAGAGATGACGTCGGGTTCTACGCGCAGTGGTGACGTCACGGGAGCGCCGGCGGCTGAGAATCCGCGTTGTTCCGTGTTGGGGGCGGCATGGAGCGGGAGCCGGGCGCCGCGGGAGTTCGCCGGGCTCTGGGCCGCCGGCTGGAGGCG... |
Task1_train_42570 | Chromosome 12 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GCTCGTCCACACCCACCCGGGCCCAGGAACCTCCTGCCTGAGAAGACGGCCCTGCTCACCTGGCCTTACTGCACGGCATCAGCCTGACCTCTGGAGGGTGGAGACTGAGGTCAGCCATATCCAGAGACCAGCCTGGTGAGGACCCTGGATACTGAGGCTTGGGGGCTCCTGGCTGGCCCCGCCTGGCACGTGTTGTCACGCATGGGTGCCGGAGAATCAAGTCCTTGGGACCCCCCGCGGGGGGACACCTGAGAGCTTGTACCTGGCCTTTCCTGGTCCCTGCCCAGGCGTCTCTTCCCTCTGCTGACTTTGACCCGTGT... | GCTCGTCCACACCCACCCGGGCCCAGGAACCTCCTGCCTGAGAAGACGGCCCTGCTCACCTGGCCTTACTGCACGGCATCAGCCTGACCTCTGGAGGGTGGAGACTGAGGTCAGCCATATCCAGAGACCAGCCTGGTGAGGACCCTGGATACTGAGGCTTGGGGGCTCCTGGCTGGCCCCGCCTGGCACGTGTTGTCACGCATGGGTGCCGGAGAATCAAGTCCTTGGGACCCCCCGCGGGGGGACACCTGAGAGCTTGTACCTGGCCTTTCCTGGTCCCTGCCCAGGCGTCTCTTCCCTCTGCTGACTTTGACCCGTGT... |
Task1_train_42571 | A mutation on Chromosome 12 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | AGGGTTCCGTGAGTATGTACATACGTGGTACTGGGTAGAATGGTGTCCACCCAGAACCTCAGGCTGCGGCCTCATCTGGAAACAGGGCCTTTGCAGGTGGAGTTGGTTAAGATGAGGCCCAGCTGATGAGGGTAGACCCTAAATCCAAACACAGGCATCCTTATAAGAAGAGAAAACAGAGACAAGGAGGAGACGCAAGGGAAGGAGGCAGAGACTGCAGCGCTGCAGCCACAGCCAGCACCTGGGTGCCAGCAGAGGCCAGACCGGGTGGCAGGATCCTCCCCTGGAGCCTCGGCCCCACGATGCCTGACTCCAGACTC... | AGGGTTCCGTGAGTATGTACATACGTGGTACTGGGTAGAATGGTGTCCACCCAGAACCTCAGGCTGCGGCCTCATCTGGAAACAGGGCCTTTGCAGGTGGAGTTGGTTAAGATGAGGCCCAGCTGATGAGGGTAGACCCTAAATCCAAACACAGGCATCCTTATAAGAAGAGAAAACAGAGACAAGGAGGAGACGCAAGGGAAGGAGGCAGAGACTGCAGCGCTGCAGCCACAGCCAGCACCTGGGTGCCAGCAGAGGCCAGACCGGGTGGCAGGATCCTCCCCTGGAGCCTCGGCCCCACGATGCCTGACTCCAGACTC... |
Task1_train_42572 | 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 | CTGGAAACAGGGCCTTTGCAGGTGGAGTTGGTTAAGATGAGGCCCAGCTGATGAGGGTAGACCCTAAATCCAAACACAGGCATCCTTATAAGAAGAGAAAACAGAGACAAGGAGGAGACGCAAGGGAAGGAGGCAGAGACTGCAGCGCTGCAGCCACAGCCAGCACCTGGGTGCCAGCAGAGGCCAGACCGGGTGGCAGGATCCTCCCCTGGAGCCTCGGCCCCACGATGCCTGACTCCAGACTCCTGGCCCCAGGCTGGGAGCACGCGTTCCGCTGCGTTTCGTCACTAGCGTGCAGCAGAGGCCTGTGAGCATTGGCC... | CTGGAAACAGGGCCTTTGCAGGTGGAGTTGGTTAAGATGAGGCCCAGCTGATGAGGGTAGACCCTAAATCCAAACACAGGCATCCTTATAAGAAGAGAAAACAGAGACAAGGAGGAGACGCAAGGGAAGGAGGCAGAGACTGCAGCGCTGCAGCCACAGCCAGCACCTGGGTGCCAGCAGAGGCCAGACCGGGTGGCAGGATCCTCCCCTGGAGCCTCGGCCCCACGATGCCTGACTCCAGACTCCTGGCCCCAGGCTGGGAGCACGCGTTCCGCTGCGTTTCGTCACTAGCGTGCAGCAGAGGCCTGTGAGCATTGGCC... |
Task1_train_42573 | This mutation occurs on Chromosome 12. Does this change lead to a known medical condition, or is it benign? | Benign | CAGGGCCTTTGCAGGTGGAGTTGGTTAAGATGAGGCCCAGCTGATGAGGGTAGACCCTAAATCCAAACACAGGCATCCTTATAAGAAGAGAAAACAGAGACAAGGAGGAGACGCAAGGGAAGGAGGCAGAGACTGCAGCGCTGCAGCCACAGCCAGCACCTGGGTGCCAGCAGAGGCCAGACCGGGTGGCAGGATCCTCCCCTGGAGCCTCGGCCCCACGATGCCTGACTCCAGACTCCTGGCCCCAGGCTGGGAGCACGCGTTCCGCTGCGTTTCGTCACTAGCGTGCAGCAGAGGCCTGTGAGCATTGGCCGCTGCCT... | CAGGGCCTTTGCAGGTGGAGTTGGTTAAGATGAGGCCCAGCTGATGAGGGTAGACCCTAAATCCAAACACAGGCATCCTTATAAGAAGAGAAAACAGAGACAAGGAGGAGACGCAAGGGAAGGAGGCAGAGACTGCAGCGCTGCAGCCACAGCCAGCACCTGGGTGCCAGCAGAGGCCAGACCGGGTGGCAGGATCCTCCCCTGGAGCCTCGGCCCCACGATGCCTGACTCCAGACTCCTGGCCCCAGGCTGGGAGCACGCGTTCCGCTGCGTTTCGTCACTAGCGTGCAGCAGAGGCCTGTGAGCATTGGCCGCTGCCT... |
Task1_train_42574 | This mutation is located on Chromosome 12. Is it associated with a disease or is it a benign polymorphism? | Benign | TTCTCCATCCCCATCCTCCCCCATGGTGGAGGCTCGCAAGGCCCTGAGGCTCGCCAGGATCTCCAGATTTGGGGAAGGTGAAAGCCGTCTTTACCCTCCTCTACCTCGAACTGGACCGCCTGACATCTCAAGCCAGGAACCACCGCGCAGGGGCGGTCATGGCGAGGGACTCACAGCCTGGGGGACGCACACCGCATTTTTTAATGGCTCTAGTTTTATCAAAAGTAAACATCCATGTGGCTTAAAAAGCCAGTTTTACGGCCAGGCGTGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGGGGATC... | TTCTCCATCCCCATCCTCCCCCATGGTGGAGGCTCGCAAGGCCCTGAGGCTCGCCAGGATCTCCAGATTTGGGGAAGGTGAAAGCCGTCTTTACCCTCCTCTACCTCGAACTGGACCGCCTGACATCTCAAGCCAGGAACCACCGCGCAGGGGCGGTCATGGCGAGGGACTCACAGCCTGGGGGACGCACACCGCATTTTTTAATGGCTCTAGTTTTATCAAAAGTAAACATCCATGTGGCTTAAAAAGCCAGTTTTACGGCCAGGCGTGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGGGGATC... |
Task1_train_42575 | This mutation on Chromosome 12 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | CAGGATCTCCAGATTTGGGGAAGGTGAAAGCCGTCTTTACCCTCCTCTACCTCGAACTGGACCGCCTGACATCTCAAGCCAGGAACCACCGCGCAGGGGCGGTCATGGCGAGGGACTCACAGCCTGGGGGACGCACACCGCATTTTTTAATGGCTCTAGTTTTATCAAAAGTAAACATCCATGTGGCTTAAAAAGCCAGTTTTACGGCCAGGCGTGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGGGGATCACTTGAGGTCAGGAGTTCGAGACCAGTCTGGCCAACACAGTGATGTAGCAGGAC... | CAGGATCTCCAGATTTGGGGAAGGTGAAAGCCGTCTTTACCCTCCTCTACCTCGAACTGGACCGCCTGACATCTCAAGCCAGGAACCACCGCGCAGGGGCGGTCATGGCGAGGGACTCACAGCCTGGGGGACGCACACCGCATTTTTTAATGGCTCTAGTTTTATCAAAAGTAAACATCCATGTGGCTTAAAAAGCCAGTTTTACGGCCAGGCGTGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGGGGATCACTTGAGGTCAGGAGTTCGAGACCAGTCTGGCCAACACAGTGATGTAGCAGGAC... |
Task1_train_42576 | This variant is found on Chromosome 12. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CAGGAGTGGTCCGATCAAGGTGCATGTTACTTGGACTTTGTCTCTGCCCAAGTTGCAGCCCCTTTGCTCCGAGGGTTGCATCGCACTCAGCACCTCCCTCCCTGCCCCCCTTGGGGTCCCAGGATGGCTGCCACTGCGGCTCCAAGTCAAACCTCCTCCGAATTGTGGGGTAGATTCCACCTCTTACTCTGACTGGACACGCTTCACCCCTCAGGGCATGCGAGAGAATGGGAGGTGAAGGTTCACAGAGGAAATTGGGGTGCTCCCTGTGAACAGAGCTGCAGATGGGAGGCCCTGGTGCTCTCTCCTGGCTTCTGTCA... | CAGGAGTGGTCCGATCAAGGTGCATGTTACTTGGACTTTGTCTCTGCCCAAGTTGCAGCCCCTTTGCTCCGAGGGTTGCATCGCACTCAGCACCTCCCTCCCTGCCCCCCTTGGGGTCCCAGGATGGCTGCCACTGCGGCTCCAAGTCAAACCTCCTCCGAATTGTGGGGTAGATTCCACCTCTTACTCTGACTGGACACGCTTCACCCCTCAGGGCATGCGAGAGAATGGGAGGTGAAGGTTCACAGAGGAAATTGGGGTGCTCCCTGTGAACAGAGCTGCAGATGGGAGGCCCTGGTGCTCTCTCCTGGCTTCTGTCA... |
Task1_train_42577 | Here is a mutation located on Chromosome 12. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GGGGAATGCAGCGGAAGGGGCTGTACTCCCTCAGCTGGATGCAGCACTGGCTGTGACACTCCTGATGGCTGCTGCAGAAGTCGCCGTTGGGCTGGGGAGGCAGCCAGGCAGCAGTCGTGGAGAGGGGCTGTCTCCGGCTACCCCTGCTCCATCTGCCCCGGGTGCCCGCAGCTCACCTTGCGCCAGGGCACACACTGCAGGAAGACGCTTTGGGGCGTGCACAACTCCTGCGGGCTGTTGTTGCGGACGCAGCAGCTGCTCTGGCACTCTGAGTCGTGCGAGCATCTGTACCCATTGGGCTATGGGACAGGAGACGCGTC... | GGGGAATGCAGCGGAAGGGGCTGTACTCCCTCAGCTGGATGCAGCACTGGCTGTGACACTCCTGATGGCTGCTGCAGAAGTCGCCGTTGGGCTGGGGAGGCAGCCAGGCAGCAGTCGTGGAGAGGGGCTGTCTCCGGCTACCCCTGCTCCATCTGCCCCGGGTGCCCGCAGCTCACCTTGCGCCAGGGCACACACTGCAGGAAGACGCTTTGGGGCGTGCACAACTCCTGCGGGCTGTTGTTGCGGACGCAGCAGCTGCTCTGGCACTCTGAGTCGTGCGAGCATCTGTACCCATTGGGCTATGGGACAGGAGACGCGTC... |
Task1_train_42578 | This variant is found on Chromosome 12. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CAGGGCTGCGTCCCCGCTAATGCCTCAGTGACCTCTGCCTCCCAGGCCTGAGGACTGGGCGCTGTGTGCCCTATTACCAGGGGCCCTCCAAGACCTGCGAGGTGTTCGGCTGGTGCCCGGTGGAAGATGGGGCCTCTGTCAGGTGCACCTGCGCCCCGGCCTGGGGCCCAGCCTCCCCTCTGATCCTTTTCCCCTGACCAGAGGCCAAACGGGCGGGGCAGGAGTGACAAGATCTGGGGAGGGGTGGGGGCCAATGCCAGGCGGGGGCTTTGCGGGAAGAGGGGACTAAACAACCCTTCTGTGCCTCCTCAGCCAATTTC... | CAGGGCTGCGTCCCCGCTAATGCCTCAGTGACCTCTGCCTCCCAGGCCTGAGGACTGGGCGCTGTGTGCCCTATTACCAGGGGCCCTCCAAGACCTGCGAGGTGTTCGGCTGGTGCCCGGTGGAAGATGGGGCCTCTGTCAGGTGCACCTGCGCCCCGGCCTGGGGCCCAGCCTCCCCTCTGATCCTTTTCCCCTGACCAGAGGCCAAACGGGCGGGGCAGGAGTGACAAGATCTGGGGAGGGGTGGGGGCCAATGCCAGGCGGGGGCTTTGCGGGAAGAGGGGACTAAACAACCCTTCTGTGCCTCCTCAGCCAATTTC... |
Task1_train_42579 | A variant was discovered on Chromosome 12. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | ACTGGCTCTTCTGGTTGAGCCGCTGCTTGGGAACCAGGGCCAGAGCTTCCCGTTTCTGACCCCTCCACCACTACTCAAATGCCCGCAGCTAGCCTCACAGTGAACCCAGGCTGACTGGCGCCCACGGCTGCACCGGGCGACCCCTGGTCCTGCTAGGTGGCCTTCCTGGGGGACGAGCGGCTGTCCCCTGGCCCCATCACTCCTCATTCCTGAGGGTTCTCCAGATTCGCTTCCAGGAATGAAGCCTAGTCAGCCAGCCTCCCTCCTCCCCTGCTTGCCCTAATTTGATTTGATCTCCACTCTGGAGGCCTCAGCACTCC... | ACTGGCTCTTCTGGTTGAGCCGCTGCTTGGGAACCAGGGCCAGAGCTTCCCGTTTCTGACCCCTCCACCACTACTCAAATGCCCGCAGCTAGCCTCACAGTGAACCCAGGCTGACTGGCGCCCACGGCTGCACCGGGCGACCCCTGGTCCTGCTAGGTGGCCTTCCTGGGGGACGAGCGGCTGTCCCCTGGCCCCATCACTCCTCATTCCTGAGGGTTCTCCAGATTCGCTTCCAGGAATGAAGCCTAGTCAGCCAGCCTCCCTCCTCCCCTGCTTGCCCTAATTTGATTTGATCTCCACTCTGGAGGCCTCAGCACTCC... |
Task1_train_42580 | This genomic variant is located on Chromosome 12. Can you determine its pathogenicity and name any linked disease? | Benign | GACCCCTCCACCACTACTCAAATGCCCGCAGCTAGCCTCACAGTGAACCCAGGCTGACTGGCGCCCACGGCTGCACCGGGCGACCCCTGGTCCTGCTAGGTGGCCTTCCTGGGGGACGAGCGGCTGTCCCCTGGCCCCATCACTCCTCATTCCTGAGGGTTCTCCAGATTCGCTTCCAGGAATGAAGCCTAGTCAGCCAGCCTCCCTCCTCCCCTGCTTGCCCTAATTTGATTTGATCTCCACTCTGGAGGCCTCAGCACTCCTCCATCTGAGCAGGCATCAGGTTTCTCCAGGCAGGCGGCCCCAGCAGCATCCAGGGG... | GACCCCTCCACCACTACTCAAATGCCCGCAGCTAGCCTCACAGTGAACCCAGGCTGACTGGCGCCCACGGCTGCACCGGGCGACCCCTGGTCCTGCTAGGTGGCCTTCCTGGGGGACGAGCGGCTGTCCCCTGGCCCCATCACTCCTCATTCCTGAGGGTTCTCCAGATTCGCTTCCAGGAATGAAGCCTAGTCAGCCAGCCTCCCTCCTCCCCTGCTTGCCCTAATTTGATTTGATCTCCACTCTGGAGGCCTCAGCACTCCTCCATCTGAGCAGGCATCAGGTTTCTCCAGGCAGGCGGCCCCAGCAGCATCCAGGGG... |
Task1_train_42581 | Here is a mutation located on Chromosome 12. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CTCCAGCACCACCAGCCCCCTGGGCCTGACTCCAGCCACCACCACCTCCAGAACCAGCAACAGACCTGCCCACACCCATCCTCACACCTGCCAGGCTATTCAGATTCCCGAGGGCACAGGAGGCCCCACCTGGACCTTGACCCCAGGACCGTCTCCTGCAGCCTCAGCTCTGACCTGCGCGGTCGAACTCTGAGCCCATCCTCGGCACTATTGCCTTGAGAAGATGTCACAGAATGGCAGAAACACCAGCCAGGTCTCATGGGCCTCGTCCTCCCGCCCACTTACCTGTGGAGTAACAGCCTGAACTGTTGATCTCAACA... | CTCCAGCACCACCAGCCCCCTGGGCCTGACTCCAGCCACCACCACCTCCAGAACCAGCAACAGACCTGCCCACACCCATCCTCACACCTGCCAGGCTATTCAGATTCCCGAGGGCACAGGAGGCCCCACCTGGACCTTGACCCCAGGACCGTCTCCTGCAGCCTCAGCTCTGACCTGCGCGGTCGAACTCTGAGCCCATCCTCGGCACTATTGCCTTGAGAAGATGTCACAGAATGGCAGAAACACCAGCCAGGTCTCATGGGCCTCGTCCTCCCGCCCACTTACCTGTGGAGTAACAGCCTGAACTGTTGATCTCAACA... |
Task1_train_42582 | A variant has been detected on Chromosome 12. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | ACAGCAGTGAGGAGCCATGCTGCTCTGTGGCCCCTACCTGAGGCAGTCCATGTGGATGCACTGGGGCGCCTTGTACTCCCCCTGGCTGTCCTTCTGGAAGCCTATCTCCTGCTGCATGCTCAGACCGTGGACTGCTGCCCGGGCCTCCACAAATGGCCTGGGTTGGAAAGAGGACAGACAAGCAAGTGGGCAGGTCAGGCTCTAATGCCCCTTTCTCCATTCCTCCCTCAGACCCAGGGAGGAACCCAGACACGGGAGGTGCAGAGTGAACCCAGGAGCCACCTCCTAAGTCGACATGGGAAGCGCCCCTGCACCACGCA... | ACAGCAGTGAGGAGCCATGCTGCTCTGTGGCCCCTACCTGAGGCAGTCCATGTGGATGCACTGGGGCGCCTTGTACTCCCCCTGGCTGTCCTTCTGGAAGCCTATCTCCTGCTGCATGCTCAGACCGTGGACTGCTGCCCGGGCCTCCACAAATGGCCTGGGTTGGAAAGAGGACAGACAAGCAAGTGGGCAGGTCAGGCTCTAATGCCCCTTTCTCCATTCCTCCCTCAGACCCAGGGAGGAACCCAGACACGGGAGGTGCAGAGTGAACCCAGGAGCCACCTCCTAAGTCGACATGGGAAGCGCCCCTGCACCACGCA... |
Task1_train_42583 | A variant affecting Chromosome 12 has been observed. Determine if it's benign or associated with disease. | Benign | AGTTTACATTTTGAAAAGTTCTTCGAATGGGATAGTGCCTGTTCATGCACATACTAAAAGTTCAGATAGTAAAAATGTGCAGGGCTGTCCTCCACAGACGCCGCCCCCCAGTCCCCAGAGCTGTCCTGGCTGCTTGTGCACAAAGAAAGTGGAGTGACAGATGCAGGTGTGGCTGCATCCAGTGGCTTCGGCCTTCCTGAGGCGTTTTCACCTGGATGCAAAAGCTCACAAGAGAAAAGGCATCTGCACTGGTGTCCGGCCCCCACATAGCAGCTTGGGGTGTTTAGGTCCCGCTGTGTTGGCCTCCGCCATGGCGCGTG... | AGTTTACATTTTGAAAAGTTCTTCGAATGGGATAGTGCCTGTTCATGCACATACTAAAAGTTCAGATAGTAAAAATGTGCAGGGCTGTCCTCCACAGACGCCGCCCCCCAGTCCCCAGAGCTGTCCTGGCTGCTTGTGCACAAAGAAAGTGGAGTGACAGATGCAGGTGTGGCTGCATCCAGTGGCTTCGGCCTTCCTGAGGCGTTTTCACCTGGATGCAAAAGCTCACAAGAGAAAAGGCATCTGCACTGGTGTCCGGCCCCCACATAGCAGCTTGGGGTGTTTAGGTCCCGCTGTGTTGGCCTCCGCCATGGCGCGTG... |
Task1_train_42584 | Given a variant located on Chromosome 12, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TAACGGATGCCAGAAAATCTTTCACAACTGAGTCAAGAAAGGGGCTTAAAAACAGCGAGCGAATCTGAGGGCACCCAGGTTGATGGCCGTCCAACCAAAACAGTGCCGTGCGCCTGGGCACAAGTGAGGGATCCTTCCGAAAGCTTGCAATTATTACCACGCGGTTTTGAAGTAATTCATTTCATTAAGTGTTTTGTGAAGGACATAACCCCCCGGGACACACGAGAATGCCTCCGTTGGGACTGGAATCGCTGCCCACAAACAAACGGAGAAACAGTCAAAGGTGGCCTAAGACCTGGGAAATCAGGAGCAGTGGTCCA... | TAACGGATGCCAGAAAATCTTTCACAACTGAGTCAAGAAAGGGGCTTAAAAACAGCGAGCGAATCTGAGGGCACCCAGGTTGATGGCCGTCCAACCAAAACAGTGCCGTGCGCCTGGGCACAAGTGAGGGATCCTTCCGAAAGCTTGCAATTATTACCACGCGGTTTTGAAGTAATTCATTTCATTAAGTGTTTTGTGAAGGACATAACCCCCCGGGACACACGAGAATGCCTCCGTTGGGACTGGAATCGCTGCCCACAAACAAACGGAGAAACAGTCAAAGGTGGCCTAAGACCTGGGAAATCAGGAGCAGTGGTCCA... |
Task1_train_42585 | A change on Chromosome 12 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TCTGTGCACGGCCGGGAACTGATGGGGGTCGACGTCTGCACATTCAAGAGCGGCCAAAACATCCTGATCGAGTTTTGATGGCTCCTCTCTAGAAAGCACAATAAAAGAAGCAAAAACATCTTTGGTAAAAACATAAAGACTTCTAAAATACCACTACTTTTTTTTTTATTTTGAGACGGAGTCTTGCTCTGTCGCCCAGGCTGGAATGCAGTGGCGTGATCTCGGCTCATCGCAAGCTCCGCCTCCCGGGTTCAAGCAATTCTCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCCTGCCACCACGCCCGGCTAA... | TCTGTGCACGGCCGGGAACTGATGGGGGTCGACGTCTGCACATTCAAGAGCGGCCAAAACATCCTGATCGAGTTTTGATGGCTCCTCTCTAGAAAGCACAATAAAAGAAGCAAAAACATCTTTGGTAAAAACATAAAGACTTCTAAAATACCACTACTTTTTTTTTTATTTTGAGACGGAGTCTTGCTCTGTCGCCCAGGCTGGAATGCAGTGGCGTGATCTCGGCTCATCGCAAGCTCCGCCTCCCGGGTTCAAGCAATTCTCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCCTGCCACCACGCCCGGCTAA... |
Task1_train_42586 | A mutation has occurred on Chromosome 12. What is the medical relevance of this mutation? | Benign | TTCTCATTTCTTTTTTCCAATGCTAAATCTTCTTTAAAATTACAATTCTTGGGCTGGGCACAGTGGCTCACACCTGTAATCTCAGCACTTTGGGAGGCTCAGGTGGGAGGACTGCTTGAAGCCAGGAGTTCAAGACCAGACTAAGCAATAAAGCGAGACCCAGTCTCTTAAAAAAAAAAAAAAAAATTTAATTACCTAGGTGTGGCCAGGCGAGGTGGCTCACGCCTGTAATCCCAGCACTTCGGGAGGCTGAGCCTGGCAGATCACTTGAGCCCAGGAGTTGGGAGACCAGCCTGGGCAACATGGGGAAACATTGTCTC... | TTCTCATTTCTTTTTTCCAATGCTAAATCTTCTTTAAAATTACAATTCTTGGGCTGGGCACAGTGGCTCACACCTGTAATCTCAGCACTTTGGGAGGCTCAGGTGGGAGGACTGCTTGAAGCCAGGAGTTCAAGACCAGACTAAGCAATAAAGCGAGACCCAGTCTCTTAAAAAAAAAAAAAAAAATTTAATTACCTAGGTGTGGCCAGGCGAGGTGGCTCACGCCTGTAATCCCAGCACTTCGGGAGGCTGAGCCTGGCAGATCACTTGAGCCCAGGAGTTGGGAGACCAGCCTGGGCAACATGGGGAAACATTGTCTC... |
Task1_train_42587 | 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 | ATCTCAGCACTTTGGGAGGCTCAGGTGGGAGGACTGCTTGAAGCCAGGAGTTCAAGACCAGACTAAGCAATAAAGCGAGACCCAGTCTCTTAAAAAAAAAAAAAAAAATTTAATTACCTAGGTGTGGCCAGGCGAGGTGGCTCACGCCTGTAATCCCAGCACTTCGGGAGGCTGAGCCTGGCAGATCACTTGAGCCCAGGAGTTGGGAGACCAGCCTGGGCAACATGGGGAAACATTGTCTCTACCAAGAATACAAAAAAACTGGCGCGTACTGGCACGTGCCCGTGATCCCAGCGATCCCAAGCTACTCCGGAGGCTGA... | ATCTCAGCACTTTGGGAGGCTCAGGTGGGAGGACTGCTTGAAGCCAGGAGTTCAAGACCAGACTAAGCAATAAAGCGAGACCCAGTCTCTTAAAAAAAAAAAAAAAAATTTAATTACCTAGGTGTGGCCAGGCGAGGTGGCTCACGCCTGTAATCCCAGCACTTCGGGAGGCTGAGCCTGGCAGATCACTTGAGCCCAGGAGTTGGGAGACCAGCCTGGGCAACATGGGGAAACATTGTCTCTACCAAGAATACAAAAAAACTGGCGCGTACTGGCACGTGCCCGTGATCCCAGCGATCCCAAGCTACTCCGGAGGCTGA... |
Task1_train_42588 | A variant was discovered on Chromosome 12. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CCAGCTACTGGGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAGGCAGAGGTTACAGTGAACCAAGATTAAGCCACTGCACTCCAGCCTGGTGACAAAGTGAGACTCCGTCTGAAAAAAAAAAAACCGAAAAAAATTCAGTGAACCCTAAGCACGGAGCGAAAGCTGGAGAGCTGGGGCACCGTGTGAGCCAGCCTGAACCACGGCCCAGCAGCAGGCCCCAGGCCAGGGTTAAACGGCCGGGCGGATGAGGCCTGTGGGGCCAAGAGAAAGCTGTTAACTGCTCCTGTTAAAATATTCCAGCCACATTTTTTTTTT... | CCAGCTACTGGGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAGGCAGAGGTTACAGTGAACCAAGATTAAGCCACTGCACTCCAGCCTGGTGACAAAGTGAGACTCCGTCTGAAAAAAAAAAAACCGAAAAAAATTCAGTGAACCCTAAGCACGGAGCGAAAGCTGGAGAGCTGGGGCACCGTGTGAGCCAGCCTGAACCACGGCCCAGCAGCAGGCCCCAGGCCAGGGTTAAACGGCCGGGCGGATGAGGCCTGTGGGGCCAAGAGAAAGCTGTTAACTGCTCCTGTTAAAATATTCCAGCCACATTTTTTTTTT... |
Task1_train_42589 | A mutation on Chromosome 12 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GAAGGACCAATCAGTGATCCTAAGAGGATAAGAAGACAAAGTGCAGTGACAGCAAGCCACCGTTCGAGAGAGTGGCTACACAGAGGAGGGGAAATGCATCCGACGGAGGGAGGCTCACGCTGTAACACTGGAGAAGTGACGACCGTACAACCAGAATTAGCCTCAAAACAGCCGAAATCACCTCTTCTGTAGACACAGCTTTAGGTGTCACAAACTGGTTGGTTTGTGTCCAAGGACCATGTTGTATGAGAAAACCATCTTCGACATGAGGCGTGCATTTAGCAAGGCAAGCTCCGGACACTGTGAGCAGCTCCAGCCCT... | GAAGGACCAATCAGTGATCCTAAGAGGATAAGAAGACAAAGTGCAGTGACAGCAAGCCACCGTTCGAGAGAGTGGCTACACAGAGGAGGGGAAATGCATCCGACGGAGGGAGGCTCACGCTGTAACACTGGAGAAGTGACGACCGTACAACCAGAATTAGCCTCAAAACAGCCGAAATCACCTCTTCTGTAGACACAGCTTTAGGTGTCACAAACTGGTTGGTTTGTGTCCAAGGACCATGTTGTATGAGAAAACCATCTTCGACATGAGGCGTGCATTTAGCAAGGCAAGCTCCGGACACTGTGAGCAGCTCCAGCCCT... |
Task1_train_42590 | A mutation found on Chromosome 12 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | ACAGGCTCCGCCCTCCAGGGCTGGGGGCGGGTTACCTCAGTTTCCAGACAGACAAGACTCCAATCCGAGGTCATGCTCCGGGACAGGAGGGGAAAATTTACAACTTTTTAGCCAAAACCAGAATTTAAAATATCTAAAACCCAGACCTTTCATTGTAGGTGATGAAAGAGTTGCATGGTACGTGCCAACGTGTTATAGTTACAAACCCAGGGCTCCACTTCCCAGGACTGAGTGTGTGGCCTCATCCTTCCTAAGCCATCAGCAGACACCGCCCGACGGCCTGGGTGCCGACCAGAGTAGGAAAGCATAATCACACAGCA... | ACAGGCTCCGCCCTCCAGGGCTGGGGGCGGGTTACCTCAGTTTCCAGACAGACAAGACTCCAATCCGAGGTCATGCTCCGGGACAGGAGGGGAAAATTTACAACTTTTTAGCCAAAACCAGAATTTAAAATATCTAAAACCCAGACCTTTCATTGTAGGTGATGAAAGAGTTGCATGGTACGTGCCAACGTGTTATAGTTACAAACCCAGGGCTCCACTTCCCAGGACTGAGTGTGTGGCCTCATCCTTCCTAAGCCATCAGCAGACACCGCCCGACGGCCTGGGTGCCGACCAGAGTAGGAAAGCATAATCACACAGCA... |
Task1_train_42591 | A mutation has occurred on Chromosome 12. What is the medical relevance of this mutation? | Benign | GCACAGAGGAAAGGATTTGTACATTTGGCTATCTACAATTTAAACATCAAAATTAAAATAAATACAACAAAAGTGAACTACTACTATAGTGGAAACATTTGCAACACAAATGAAAATGTGCTATACCCTTAATTAACAAAGATATCGGCCAGGCACGGTGGCTCGCGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGATCACAAGGTCAGGAGTTCGAGACCAGCCTAACCAAGATGGTGAAACCTCACCTCTACTAAAAATACAAAAAAAAAATTAGCTGGGCATGTTGGCGGGTGCCTGTAATCCCAGCT... | GCACAGAGGAAAGGATTTGTACATTTGGCTATCTACAATTTAAACATCAAAATTAAAATAAATACAACAAAAGTGAACTACTACTATAGTGGAAACATTTGCAACACAAATGAAAATGTGCTATACCCTTAATTAACAAAGATATCGGCCAGGCACGGTGGCTCGCGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGATCACAAGGTCAGGAGTTCGAGACCAGCCTAACCAAGATGGTGAAACCTCACCTCTACTAAAAATACAAAAAAAAAATTAGCTGGGCATGTTGGCGGGTGCCTGTAATCCCAGCT... |
Task1_train_42592 | This variant is present on Chromosome 12. Is the change likely to result in a pathogenic outcome? | Benign | TTTTTTGAGACAGAGTCTTGCTCTGTGGCCTAGGCTGGAGTATAGTGGAGCAATCTCGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCCAGTAGCTGGGATTACAGATGCCCACAACTGGCCAATTTTTTCATTTTTAGTAAAGATGGGGTCTCACCGCGTTGGTCAGGCTGGTCTCAAACTCCTGACCTCAGGTCATCCGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCCATGCCCAGCCTAGGTGGCCTTTTTCTACCTAGGTATTTTTCCATGTTGTC... | TTTTTTGAGACAGAGTCTTGCTCTGTGGCCTAGGCTGGAGTATAGTGGAGCAATCTCGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCCAGTAGCTGGGATTACAGATGCCCACAACTGGCCAATTTTTTCATTTTTAGTAAAGATGGGGTCTCACCGCGTTGGTCAGGCTGGTCTCAAACTCCTGACCTCAGGTCATCCGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCCATGCCCAGCCTAGGTGGCCTTTTTCTACCTAGGTATTTTTCCATGTTGTC... |
Task1_train_42593 | This variant is found on Chromosome 12. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TAGTTTACTAGATTAAGTTGTGTGACTTACACAATTTTTCATGTTTGCTAGAATTAAAATTTCCTCATTCCTGTGCTTATTTTTCCTGTGTAACTGTTGCTGACTCTTTCCACACCTTCCCCACACCGATCAACCCCACGTGTCAGATAACCTAATTTCTTTCCCTGGGGACCCCTCCTAGAACCTTCCTGTCACAGTGCCCCAGTGGCTGGCTGCTCTCTGGACTGCTATACAGCAATGCTTCTACCATAACATTCCCAAATGTTTTCTAATAATCTTAACTTTGGCTTTCAAAGTGCAGACTTCTCCCTAAATCATCT... | TAGTTTACTAGATTAAGTTGTGTGACTTACACAATTTTTCATGTTTGCTAGAATTAAAATTTCCTCATTCCTGTGCTTATTTTTCCTGTGTAACTGTTGCTGACTCTTTCCACACCTTCCCCACACCGATCAACCCCACGTGTCAGATAACCTAATTTCTTTCCCTGGGGACCCCTCCTAGAACCTTCCTGTCACAGTGCCCCAGTGGCTGGCTGCTCTCTGGACTGCTATACAGCAATGCTTCTACCATAACATTCCCAAATGTTTTCTAATAATCTTAACTTTGGCTTTCAAAGTGCAGACTTCTCCCTAAATCATCT... |
Task1_train_42594 | 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 | CTGGGGAAAGCTACAAATTAACAACATCTCAGCAAAGCAATTGTTTAAAGTACAGGTCTTTTTCAAAATGGAGTCTCTTATGTCTTCCCTTTCTACATAGGCACAGTGACAGTCTGATCTCTCTTTCTTTTCCCTACATTTCCCCCTTTTCTTTTTGACAAAACCGCCATCGTCATCATGACCCGTTCTCGCTGGTCGCTGTCTCTCCGGAGCTGTTGTATACACCTGTAGACTAATAATAGAAAGGACAGACATACAAGGATTAATACAAAATTTGTAATAGTGGAATTTCCAGTGGTTTTAACCCAAGTGACAGGGTT... | CTGGGGAAAGCTACAAATTAACAACATCTCAGCAAAGCAATTGTTTAAAGTACAGGTCTTTTTCAAAATGGAGTCTCTTATGTCTTCCCTTTCTACATAGGCACAGTGACAGTCTGATCTCTCTTTCTTTTCCCTACATTTCCCCCTTTTCTTTTTGACAAAACCGCCATCGTCATCATGACCCGTTCTCGCTGGTCGCTGTCTCTCCGGAGCTGTTGTATACACCTGTAGACTAATAATAGAAAGGACAGACATACAAGGATTAATACAAAATTTGTAATAGTGGAATTTCCAGTGGTTTTAACCCAAGTGACAGGGTT... |
Task1_train_42595 | A mutation on Chromosome 12 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CCATCCTCTGAGGCTAACATGAATAACTACAACAGCAGCTACTGCCTTCTTTCTTCCACCGTATGCCACTCCTTCCATATTTTGTTAGAACTAATCTGGTCAGTATCTGCAAGATCAAGCAGCAAAATCTCATGCTTTACTTAGCATTTAAAATTGGTAACTTCCCCTCTGTCTGAAAACTTTCTGTAGTTCCAATGCTGAAATGTTGGGATACTCTTTTTGCTGTTCTAAACACTTGCTTTCAGTGATCTTGGTTCTATCTTCATCTGCTGCTTAAGCATAAAAGCTCGGTCAACATTCCTTTTCCATACTTTTTTTCT... | CCATCCTCTGAGGCTAACATGAATAACTACAACAGCAGCTACTGCCTTCTTTCTTCCACCGTATGCCACTCCTTCCATATTTTGTTAGAACTAATCTGGTCAGTATCTGCAAGATCAAGCAGCAAAATCTCATGCTTTACTTAGCATTTAAAATTGGTAACTTCCCCTCTGTCTGAAAACTTTCTGTAGTTCCAATGCTGAAATGTTGGGATACTCTTTTTGCTGTTCTAAACACTTGCTTTCAGTGATCTTGGTTCTATCTTCATCTGCTGCTTAAGCATAAAAGCTCGGTCAACATTCCTTTTCCATACTTTTTTTCT... |
Task1_train_42596 | A mutation on Chromosome 12 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TGGTGGATCACCTGAGCCCAGGAGGTCGAGGTTGCAATGAGCCATGACCACACCACTGCATTCTAGCCTGAGAGACAGAGACTCTGTCTGAAAAATTGAAAAAAAAAAAGAAAAAATCAATTAACATATTTTTCTTGGCCGGGCACAGTGGCTCACGCCTGTAATGCCAACACTTTGGGACGCCTAGGTGGGTGGATCACCTGAGGTCAGGAGTTTGAGACCAACCTGGCCAACATGGTGAAACCCCGTCTCTATTAAAAATACTAAAATTAGCCAGGCATGGCGGTGGTGCCTGTAATCCCAGCTACTCAGGAGGCTGA... | TGGTGGATCACCTGAGCCCAGGAGGTCGAGGTTGCAATGAGCCATGACCACACCACTGCATTCTAGCCTGAGAGACAGAGACTCTGTCTGAAAAATTGAAAAAAAAAAAGAAAAAATCAATTAACATATTTTTCTTGGCCGGGCACAGTGGCTCACGCCTGTAATGCCAACACTTTGGGACGCCTAGGTGGGTGGATCACCTGAGGTCAGGAGTTTGAGACCAACCTGGCCAACATGGTGAAACCCCGTCTCTATTAAAAATACTAAAATTAGCCAGGCATGGCGGTGGTGCCTGTAATCCCAGCTACTCAGGAGGCTGA... |
Task1_train_42597 | 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 | GGCCCCAGGTGTTCCTTGGCTTGTGGATATATCATTCCAGTCTTGGTCTCCATGTTCACATGGTCTCTTCCCCTGTGTCTGTGTCTTTTTTATGGAGGACCACCCTCATACTGGATTAGGGGCCCATCCTATTTCTGGTACTACCTCATCATAACTAATTACATCTGGAAAGACTGTATTTCCAAATATGGTCATATTCTGAGATACTGAGGATTAAAACTTCAACATACCTTTTTGTCGGCGGGGGGGATACAGTTTAACCCATAATACCAGGTAAGAGTGGAATGTCACCCCACTTATGTAAGATGAAGTGGTATCAT... | GGCCCCAGGTGTTCCTTGGCTTGTGGATATATCATTCCAGTCTTGGTCTCCATGTTCACATGGTCTCTTCCCCTGTGTCTGTGTCTTTTTTATGGAGGACCACCCTCATACTGGATTAGGGGCCCATCCTATTTCTGGTACTACCTCATCATAACTAATTACATCTGGAAAGACTGTATTTCCAAATATGGTCATATTCTGAGATACTGAGGATTAAAACTTCAACATACCTTTTTGTCGGCGGGGGGGATACAGTTTAACCCATAATACCAGGTAAGAGTGGAATGTCACCCCACTTATGTAAGATGAAGTGGTATCAT... |
Task1_train_42598 | A mutation found on Chromosome 12 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TTTAGTGCTATAAATTTCCCTCTACACACTGCTTTGAATGTGTCCCAGAGATTCTGGTATGTTGTGTCTTTGTTCTCATTGGTTTCAAAGAACATCTTTATTTCTGCCTTCATTTCGTTATGTACCCCATAGTCATTCAGGAGCAGGTTGTTCAGTTTCCATGTAGTTGAGCGGTTTTGAGTGAGTTTCTTAATCCTGAGTTCTAGTTTGATTGCACTGTCGTCTTAGAGATAGTTTGTTATAATTTCTGTTCTTTTACATTTGCTGAGGAGAGCTTTACTTCCAAATATGTGGTCAATTTTGGAATAGGTGTGATGTGG... | TTTAGTGCTATAAATTTCCCTCTACACACTGCTTTGAATGTGTCCCAGAGATTCTGGTATGTTGTGTCTTTGTTCTCATTGGTTTCAAAGAACATCTTTATTTCTGCCTTCATTTCGTTATGTACCCCATAGTCATTCAGGAGCAGGTTGTTCAGTTTCCATGTAGTTGAGCGGTTTTGAGTGAGTTTCTTAATCCTGAGTTCTAGTTTGATTGCACTGTCGTCTTAGAGATAGTTTGTTATAATTTCTGTTCTTTTACATTTGCTGAGGAGAGCTTTACTTCCAAATATGTGGTCAATTTTGGAATAGGTGTGATGTGG... |
Task1_train_42599 | Given this variant on Chromosome 12, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TAGTGCTATAAATTTCCCTCTACACACTGCTTTGAATGTGTCCCAGAGATTCTGGTATGTTGTGTCTTTGTTCTCATTGGTTTCAAAGAACATCTTTATTTCTGCCTTCATTTCGTTATGTACCCCATAGTCATTCAGGAGCAGGTTGTTCAGTTTCCATGTAGTTGAGCGGTTTTGAGTGAGTTTCTTAATCCTGAGTTCTAGTTTGATTGCACTGTCGTCTTAGAGATAGTTTGTTATAATTTCTGTTCTTTTACATTTGCTGAGGAGAGCTTTACTTCCAAATATGTGGTCAATTTTGGAATAGGTGTGATGTGGTG... | TAGTGCTATAAATTTCCCTCTACACACTGCTTTGAATGTGTCCCAGAGATTCTGGTATGTTGTGTCTTTGTTCTCATTGGTTTCAAAGAACATCTTTATTTCTGCCTTCATTTCGTTATGTACCCCATAGTCATTCAGGAGCAGGTTGTTCAGTTTCCATGTAGTTGAGCGGTTTTGAGTGAGTTTCTTAATCCTGAGTTCTAGTTTGATTGCACTGTCGTCTTAGAGATAGTTTGTTATAATTTCTGTTCTTTTACATTTGCTGAGGAGAGCTTTACTTCCAAATATGTGGTCAATTTTGGAATAGGTGTGATGTGGTG... |
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