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_42700 | Chromosome 13 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | AAAATAATTAAATATCTTGCACGCTTACTCCAAATTCCACCGTGAAAATGATGTCTTTTCATAACTCCTATAATAGCATTTTAATCAAGGTTAGTAACAGACTGGAAAATTTGTGAAAAGAACATTACTTTAAAAATCAACATGAAAGATTTCACAACTTTTTTAGCCAGTCAGCTTCAAAGACACAATTTGATTCAATAAGCGTTACTGGCATATTATTTCCAATCTACGTGAAAAAACGCTTGGTTTAATAATGTACTTTAGGCTTTCTGTATCTTTTTGGTAAGGAAAGAAAGGAACAGGTGGAGTAGATTAGCCAG... | AAAATAATTAAATATCTTGCACGCTTACTCCAAATTCCACCGTGAAAATGATGTCTTTTCATAACTCCTATAATAGCATTTTAATCAAGGTTAGTAACAGACTGGAAAATTTGTGAAAAGAACATTACTTTAAAAATCAACATGAAAGATTTCACAACTTTTTTAGCCAGTCAGCTTCAAAGACACAATTTGATTCAATAAGCGTTACTGGCATATTATTTCCAATCTACGTGAAAAAACGCTTGGTTTAATAATGTACTTTAGGCTTTCTGTATCTTTTTGGTAAGGAAAGAAAGGAACAGGTGGAGTAGATTAGCCAG... |
Task1_train_42701 | Given this variant on Chromosome 13, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GGCAGGAGAATCACCTCAACCTGGGAGGTGGAGGTTGCAATGAGCCAAGATCACGCCATTGCACTCCAGCCTGAGCAACAGAGACTCTGTCTCAACAAATTAAAAAAAAAAATAAATAAAGTGCCCAGATTATAGGTGTGAGCTACCCTGCTCAGCCTAAAGTATTTTTTAATCAAGGTATGTAAGTTGTTTTTTAAGACATAATGGTATTGCACACTTACTAGACTATGGTATAATGTAAAAATAACTTTTTTGCCCCATAGGATCTGCAGGAAAACATACTTTTACATGCAACGGAAAACCAAAAAAAAAATAATTGT... | GGCAGGAGAATCACCTCAACCTGGGAGGTGGAGGTTGCAATGAGCCAAGATCACGCCATTGCACTCCAGCCTGAGCAACAGAGACTCTGTCTCAACAAATTAAAAAAAAAAATAAATAAAGTGCCCAGATTATAGGTGTGAGCTACCCTGCTCAGCCTAAAGTATTTTTTAATCAAGGTATGTAAGTTGTTTTTTAAGACATAATGGTATTGCACACTTACTAGACTATGGTATAATGTAAAAATAACTTTTTTGCCCCATAGGATCTGCAGGAAAACATACTTTTACATGCAACGGAAAACCAAAAAAAAAATAATTGT... |
Task1_train_42702 | A variant was discovered on Chromosome 13. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TCTGAAGACCGATTTAGTGATCCCTGAGGTGTGTTAGTAATGATAGAACCAGGGCCCATGGAAGTAAGGGTCTTGAAGGAGCTTTCATGTATTAATGAAAAATAAGCAGTTCCTGAATTATTTATTCTTTCTTCCTGAGAATGTCAGCGGCATTTGAACCAGAGCAACTCCATCTCGAGAGAGAGCTAGGAAAAATGGGGATGGGATTTGCTGGGCTGCATTCCCAGGAGGTTAGGTATTCCTAGCCTCTAGATGTTTACATTTAATGAAACAGATTAGTAATGTTTACTAAACACACCCAGGCCCAGGAATGTCCTGAT... | TCTGAAGACCGATTTAGTGATCCCTGAGGTGTGTTAGTAATGATAGAACCAGGGCCCATGGAAGTAAGGGTCTTGAAGGAGCTTTCATGTATTAATGAAAAATAAGCAGTTCCTGAATTATTTATTCTTTCTTCCTGAGAATGTCAGCGGCATTTGAACCAGAGCAACTCCATCTCGAGAGAGAGCTAGGAAAAATGGGGATGGGATTTGCTGGGCTGCATTCCCAGGAGGTTAGGTATTCCTAGCCTCTAGATGTTTACATTTAATGAAACAGATTAGTAATGTTTACTAAACACACCCAGGCCCAGGAATGTCCTGAT... |
Task1_train_42703 | A variant was discovered on Chromosome 13. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GAGGAAATGGAAATCGAAAAGTGACCTAAGAAGTATTCAGCTCTTGAAATGGCTTGGCTATAAGTCCCTCCCAGTGCACAAGGCACCATGGAGAAGTCCTGTTGGTGTGGAGGGAATTCTAGCAGTTAGGGTCGTGCCCTGACCAAATGGCTTTGTATTCACAAGTGACTCTGGGAGGCTTTTCCATAAAATCTTCTCCTAGGTCAATGAGACTGCAGTTTTGCTGATGAATTCCCTCGGGGACTAAGCCCTTCCTCTGTGGGTAACATTTTTCCTCTGGAGCAGCTGCCCCTGGGGGAAGGAATCAGTTTGCGGGTAGG... | GAGGAAATGGAAATCGAAAAGTGACCTAAGAAGTATTCAGCTCTTGAAATGGCTTGGCTATAAGTCCCTCCCAGTGCACAAGGCACCATGGAGAAGTCCTGTTGGTGTGGAGGGAATTCTAGCAGTTAGGGTCGTGCCCTGACCAAATGGCTTTGTATTCACAAGTGACTCTGGGAGGCTTTTCCATAAAATCTTCTCCTAGGTCAATGAGACTGCAGTTTTGCTGATGAATTCCCTCGGGGACTAAGCCCTTCCTCTGTGGGTAACATTTTTCCTCTGGAGCAGCTGCCCCTGGGGGAAGGAATCAGTTTGCGGGTAGG... |
Task1_train_42704 | A variant on Chromosome 13 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | CTGATTGACAAGCACACAGATGAAACTCAATCCTGTTTTTACCTCCTCCATGTTTCACAGTGAATTCCCTACTATCCTAGGCAGATGGCTAAAGGGTTGGGTTGGGCTGGTGGCTGCTATGGACACAAATCTATAAATTGTTCTAAAATCTAGCTACTCAAAGTGTGGTCCATGGATAAGGGAGCTTGTTAAAAAGACCAAATCTGGCCAGGCACGGTGGCTCACGCCTATAATCCCAGCAATTTGGGAAGCTGAGGAGGGAGGATTGCTTGAGCCCAGAAGTTGAGACAATCCTGGTCAACAGAGTGAGACCTGATCTC... | CTGATTGACAAGCACACAGATGAAACTCAATCCTGTTTTTACCTCCTCCATGTTTCACAGTGAATTCCCTACTATCCTAGGCAGATGGCTAAAGGGTTGGGTTGGGCTGGTGGCTGCTATGGACACAAATCTATAAATTGTTCTAAAATCTAGCTACTCAAAGTGTGGTCCATGGATAAGGGAGCTTGTTAAAAAGACCAAATCTGGCCAGGCACGGTGGCTCACGCCTATAATCCCAGCAATTTGGGAAGCTGAGGAGGGAGGATTGCTTGAGCCCAGAAGTTGAGACAATCCTGGTCAACAGAGTGAGACCTGATCTC... |
Task1_train_42705 | A mutation has occurred on Chromosome 13. What is the medical relevance of this mutation? | Benign | ATGTTAAGAATGCTTGATTCATACCGTGCAAGAGAAAAAGCCCTGAATGCTATTTTTCAGTATTAGAATTACATTTGATACTTGAACAGCAGGGATATTAGGATTCCAAGAGAGAGCTTAATGGTAGGCATACAGAAAAGAGAGTTTCCCAGCAGTAGTGGAATTACCTCTCCAATGCAACAACTAAATTTCCAGGAAGGGAGTAGGAATCAAGGATGGTACATCTGATTTGATGGAGAGGGACATAAAGGTAAAATGTCTGTGTGGCTGCTGAGAATGCCCAGCTTTTAGGATGTAGGTTGTGTGTAATCAGATTTTTA... | ATGTTAAGAATGCTTGATTCATACCGTGCAAGAGAAAAAGCCCTGAATGCTATTTTTCAGTATTAGAATTACATTTGATACTTGAACAGCAGGGATATTAGGATTCCAAGAGAGAGCTTAATGGTAGGCATACAGAAAAGAGAGTTTCCCAGCAGTAGTGGAATTACCTCTCCAATGCAACAACTAAATTTCCAGGAAGGGAGTAGGAATCAAGGATGGTACATCTGATTTGATGGAGAGGGACATAAAGGTAAAATGTCTGTGTGGCTGCTGAGAATGCCCAGCTTTTAGGATGTAGGTTGTGTGTAATCAGATTTTTA... |
Task1_train_42706 | A sequence alteration has been identified on Chromosome 13. Is it disease-inducing or harmless? | Benign | CTGGGGTGAATGTTTAAGGGGCTGCTAGCAGAAAAGACTCAAGGGTGGCTAAGAGTGAAGGATATGCCCAGATGGGCAAGAGAGAAGGCTGGGCTGACCAACGGCACCGCCATTTTGGACACAGCAATTTGGGTGGCTGTTTGGATGATTCATGCTGCTTCTCTGCTCATGCTAAGTGTGAGTACACATCTGTGGGTGGTGGCCCTTGAGAACAGTGTTTGTTCCTCCTTTAGGGTGACAGAATGTGCCAGAGCCCATGCTTAGTGCTTTTGTACATTGCCTTTTTTAATCCTAAAAATGTCTCTATGAGGCAAGGAGTA... | CTGGGGTGAATGTTTAAGGGGCTGCTAGCAGAAAAGACTCAAGGGTGGCTAAGAGTGAAGGATATGCCCAGATGGGCAAGAGAGAAGGCTGGGCTGACCAACGGCACCGCCATTTTGGACACAGCAATTTGGGTGGCTGTTTGGATGATTCATGCTGCTTCTCTGCTCATGCTAAGTGTGAGTACACATCTGTGGGTGGTGGCCCTTGAGAACAGTGTTTGTTCCTCCTTTAGGGTGACAGAATGTGCCAGAGCCCATGCTTAGTGCTTTTGTACATTGCCTTTTTTAATCCTAAAAATGTCTCTATGAGGCAAGGAGTA... |
Task1_train_42707 | Chromosome 13 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GTCAAACCAAAAGGTAGAGGGTACACACATTATAACAATGTGAAAAACATCTTTTCATCAGAAAACTGTATCTCTTAATTATTCAAATACTTGATAATATCAAAAGAAAACAAAAATAAAATTTAATTAGTTAAATTAAACTTTAATAGCAAGAATACAATCTGGACAGCAATTATGAGAACAGCTTATAAGATCACAATAAAAATATGACAAATAAAAGCTACTACTAACATACTAATGTTGACTGTGTATTATTTTTGATAATTTAAAACTTTAAAACTCAGACAAATCTAACTTCAAAAGATTTTGAAGTTATATTT... | GTCAAACCAAAAGGTAGAGGGTACACACATTATAACAATGTGAAAAACATCTTTTCATCAGAAAACTGTATCTCTTAATTATTCAAATACTTGATAATATCAAAAGAAAACAAAAATAAAATTTAATTAGTTAAATTAAACTTTAATAGCAAGAATACAATCTGGACAGCAATTATGAGAACAGCTTATAAGATCACAATAAAAATATGACAAATAAAAGCTACTACTAACATACTAATGTTGACTGTGTATTATTTTTGATAATTTAAAACTTTAAAACTCAGACAAATCTAACTTCAAAAGATTTTGAAGTTATATTT... |
Task1_train_42708 | Given this variant on Chromosome 13, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | ATCATAGATCCAATCGTCCCCACCTCCAGGAGCTAGGTCTAAAAGAAGAAGAAAGAAATTGTTGAAATACAGACGTTTCAAATTAATTTACAAACTGGGAATTGTTTGATTTAAATGTTTATTTGTTTGTATACCTTTAGATTTTTTTCAGTTTTTAACTAATATAAACAACTTTACAATGAGTACCCTTGTTTATACATAATTGCTTCTTTGTCTCTTTAGAATATTCTTCCCTAGAATAGATTTGCTAGTCTAAGGCTCTGTACTTTTTGCAATTACGGCATGTTCCCAAATGGACGTCAAAAGAACTGAATTCATTT... | ATCATAGATCCAATCGTCCCCACCTCCAGGAGCTAGGTCTAAAAGAAGAAGAAAGAAATTGTTGAAATACAGACGTTTCAAATTAATTTACAAACTGGGAATTGTTTGATTTAAATGTTTATTTGTTTGTATACCTTTAGATTTTTTTCAGTTTTTAACTAATATAAACAACTTTACAATGAGTACCCTTGTTTATACATAATTGCTTCTTTGTCTCTTTAGAATATTCTTCCCTAGAATAGATTTGCTAGTCTAAGGCTCTGTACTTTTTGCAATTACGGCATGTTCCCAAATGGACGTCAAAAGAACTGAATTCATTT... |
Task1_train_42709 | A variant has been detected on Chromosome 13. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CTAGGGCAGAGGTTTGGCAGGAGGTTAGCAGTGAGAAAAGCCATTTGGCAGAAAAAGTACTTGGCAAGTTGTGATGGTTAACATATATTCACTGGGTCCTATGATGTGCCAGCCCTGTGCCGGATTTTGGCTTGGTGATGCAGTCATGCACAAATTGGTCTCAGCTCTGCCTTTGCGGAAAGAGAAGGATCTAAATTTGCCTCCCGAGAGTACATGAATGAGAAGCTTAGAAAGAAATGACTGGCTTCAAGCTTCTCAAAGTGTAGTGTAGTGGATTTCCACTGAGACTAGATTATAAGATTTTTGAAATCCTTATTGAG... | CTAGGGCAGAGGTTTGGCAGGAGGTTAGCAGTGAGAAAAGCCATTTGGCAGAAAAAGTACTTGGCAAGTTGTGATGGTTAACATATATTCACTGGGTCCTATGATGTGCCAGCCCTGTGCCGGATTTTGGCTTGGTGATGCAGTCATGCACAAATTGGTCTCAGCTCTGCCTTTGCGGAAAGAGAAGGATCTAAATTTGCCTCCCGAGAGTACATGAATGAGAAGCTTAGAAAGAAATGACTGGCTTCAAGCTTCTCAAAGTGTAGTGTAGTGGATTTCCACTGAGACTAGATTATAAGATTTTTGAAATCCTTATTGAG... |
Task1_train_42710 | The following genetic variant occurs on Chromosome 13. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | ATTAGCTCTATCTCATTTTCAGATATTGAATTACTTGTTTCATCTAAATTAGTACTTCCATATAGTGTACAATCAGACTGTGTCCCTTCTCCAAGCTCAACCTAGGCCTGCTAATTCTTACACAAGCCAAGGGAAGGAGGGGCCTGATCAGTTCTTCAACCCTATTTTTTTACTCTCTTTTTCTATTCTTTTCATTTTTCCTTTTTCTTTTTTTTTTGACAGGGTCTCACTCCGTCACCCAAGTTGAAGTGCAGTGGTACAATCATGGCTCACTGCAGCCTCAATCTCCTGGGCTCATGGTACCCTCCCACCTCAGCCTT... | ATTAGCTCTATCTCATTTTCAGATATTGAATTACTTGTTTCATCTAAATTAGTACTTCCATATAGTGTACAATCAGACTGTGTCCCTTCTCCAAGCTCAACCTAGGCCTGCTAATTCTTACACAAGCCAAGGGAAGGAGGGGCCTGATCAGTTCTTCAACCCTATTTTTTTACTCTCTTTTTCTATTCTTTTCATTTTTCCTTTTTCTTTTTTTTTTGACAGGGTCTCACTCCGTCACCCAAGTTGAAGTGCAGTGGTACAATCATGGCTCACTGCAGCCTCAATCTCCTGGGCTCATGGTACCCTCCCACCTCAGCCTT... |
Task1_train_42711 | A variant on Chromosome 13 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TTTTTTTTTTGACAGGGTCTCACTCCGTCACCCAAGTTGAAGTGCAGTGGTACAATCATGGCTCACTGCAGCCTCAATCTCCTGGGCTCATGGTACCCTCCCACCTCAGCCTTCTGAGTATCTGGGAGTACAGGAGCATGATGCCACACTTGGCTAATTATTTTTTTTTTGTAGGGATAGGAGTATTGCTATGTTGCCCAGGCTGGTCTTGAACTCCTGGCCTCAAGCGATCCTGCTATCTCAGCATCCCAAAGTGCTGGGATTACAGGCATGAGCTACTGTGCCTGGCCCTACTCTCTTTCTCAACTCATATTATAGTT... | TTTTTTTTTTGACAGGGTCTCACTCCGTCACCCAAGTTGAAGTGCAGTGGTACAATCATGGCTCACTGCAGCCTCAATCTCCTGGGCTCATGGTACCCTCCCACCTCAGCCTTCTGAGTATCTGGGAGTACAGGAGCATGATGCCACACTTGGCTAATTATTTTTTTTTTGTAGGGATAGGAGTATTGCTATGTTGCCCAGGCTGGTCTTGAACTCCTGGCCTCAAGCGATCCTGCTATCTCAGCATCCCAAAGTGCTGGGATTACAGGCATGAGCTACTGTGCCTGGCCCTACTCTCTTTCTCAACTCATATTATAGTT... |
Task1_train_42712 | A genomic change on Chromosome 13 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | ACAGAATGAAATGCTAGTATATGCTACAACAACAATGAGCCTTGAAAACATTATGCTAGGTGGAATAAGTCAGATACAGAAGGATAAACATTGTGTTATTGTGCTTATATAAGGTACCTAGAATAGACAAATTTACAGACACAGAAAGTGGAATATAGGTTACTGGGGGCTCAGGTATAGCAGAGAGGGGAGAATTGGGAGTAGCTGTTCAATGGATATAGAGTTTCTGTTTGGGATGATGGGAAAGTTCTGGAAATACATATAGTGCTGGTGGTTGCATAATACTGTAATTGTAATTAATGCTGCTGAATGGCACACTT... | ACAGAATGAAATGCTAGTATATGCTACAACAACAATGAGCCTTGAAAACATTATGCTAGGTGGAATAAGTCAGATACAGAAGGATAAACATTGTGTTATTGTGCTTATATAAGGTACCTAGAATAGACAAATTTACAGACACAGAAAGTGGAATATAGGTTACTGGGGGCTCAGGTATAGCAGAGAGGGGAGAATTGGGAGTAGCTGTTCAATGGATATAGAGTTTCTGTTTGGGATGATGGGAAAGTTCTGGAAATACATATAGTGCTGGTGGTTGCATAATACTGTAATTGTAATTAATGCTGCTGAATGGCACACTT... |
Task1_train_42713 | This variant is located on Chromosome 13. Evaluate its biological effect and specify any disease association. | Benign | AGAATGAAATGCTAGTATATGCTACAACAACAATGAGCCTTGAAAACATTATGCTAGGTGGAATAAGTCAGATACAGAAGGATAAACATTGTGTTATTGTGCTTATATAAGGTACCTAGAATAGACAAATTTACAGACACAGAAAGTGGAATATAGGTTACTGGGGGCTCAGGTATAGCAGAGAGGGGAGAATTGGGAGTAGCTGTTCAATGGATATAGAGTTTCTGTTTGGGATGATGGGAAAGTTCTGGAAATACATATAGTGCTGGTGGTTGCATAATACTGTAATTGTAATTAATGCTGCTGAATGGCACACTTAA... | AGAATGAAATGCTAGTATATGCTACAACAACAATGAGCCTTGAAAACATTATGCTAGGTGGAATAAGTCAGATACAGAAGGATAAACATTGTGTTATTGTGCTTATATAAGGTACCTAGAATAGACAAATTTACAGACACAGAAAGTGGAATATAGGTTACTGGGGGCTCAGGTATAGCAGAGAGGGGAGAATTGGGAGTAGCTGTTCAATGGATATAGAGTTTCTGTTTGGGATGATGGGAAAGTTCTGGAAATACATATAGTGCTGGTGGTTGCATAATACTGTAATTGTAATTAATGCTGCTGAATGGCACACTTAA... |
Task1_train_42714 | Consider this mutation on Chromosome 13. Is this a benign change or a disease-causing variant? | Benign | GGGTGCTCAGCTGCCAAGGCAGTCTCAACACAGAGCTATTCTAGCTTTAAGGATGGCTTAGCAGCCAGGTGCAGTGGCTCACACCTGTAATCCTAGCACTTTGGGAGGCCGAGGAGGGTGTATTGCCTGAGGTCAGGCATTCAAGACTAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAAGACGAAAATTAGCCAGGCGTGGTGGTGGTGGATGCCTGTAATCCCAGCTACTCGTGAGACTGAGTCAGGAGAATCACTTGAACCCAGGGGGCAGAGCTTGCAGTGAGCCGAGATCAGGCCACTTCACTCCAGC... | GGGTGCTCAGCTGCCAAGGCAGTCTCAACACAGAGCTATTCTAGCTTTAAGGATGGCTTAGCAGCCAGGTGCAGTGGCTCACACCTGTAATCCTAGCACTTTGGGAGGCCGAGGAGGGTGTATTGCCTGAGGTCAGGCATTCAAGACTAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAAGACGAAAATTAGCCAGGCGTGGTGGTGGTGGATGCCTGTAATCCCAGCTACTCGTGAGACTGAGTCAGGAGAATCACTTGAACCCAGGGGGCAGAGCTTGCAGTGAGCCGAGATCAGGCCACTTCACTCCAGC... |
Task1_train_42715 | A mutation found on Chromosome 13 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AGTTGAACAGAAAACCCACACAATCAGGAAGACCCATTAAACAGCTATATATGCCACAACTAATTACTTCCTTATGGGGTGCTCCATGTGGGCTGAAGATCACTTCCCTAACAGGTGCCTTCCTGGGAAGAAGCCTCTATTATCACATTGGAGAGGAACAAAGTCTCAGACAAATCCCATACTGCAGTTATTTAAATGACCTCATTCTTCCTCAAAATAGAAAATCAAAAGCATCACTTCCTGGCAACTGCTGTGCACTCTTCCTTAATATCAAAGATATGTAACACACACAGGCTCATCAGTGCCTTACAAACATACAA... | AGTTGAACAGAAAACCCACACAATCAGGAAGACCCATTAAACAGCTATATATGCCACAACTAATTACTTCCTTATGGGGTGCTCCATGTGGGCTGAAGATCACTTCCCTAACAGGTGCCTTCCTGGGAAGAAGCCTCTATTATCACATTGGAGAGGAACAAAGTCTCAGACAAATCCCATACTGCAGTTATTTAAATGACCTCATTCTTCCTCAAAATAGAAAATCAAAAGCATCACTTCCTGGCAACTGCTGTGCACTCTTCCTTAATATCAAAGATATGTAACACACACAGGCTCATCAGTGCCTTACAAACATACAA... |
Task1_train_42716 | Given this context: Chromosome 13 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CCATACAGTATCTGTTTCAACCACTCTCTTCTGCCGCTGTAGTGAGAAAGCAGCTATAGACACAAGAGAAATTCATTTATAAAAACAGGAAGCTGGCAGGATTTGGTCCACAGGTCATAGTTTGCAGACTCTGAGTATAGAGGAAAGAGCACAGAGAAGAATCGGAACAGAGTGGATTCCAGTTCCAGCTGTCCGTTCACCAGCTGTGCCTCTGCATCAAAACGCTCTCAGCCCTTAAATTGGGATATTTATCAGGACACTAAGGAGATAAAGGAAGGTGAAAGTGCTTGTAAATGTGTAGTTCCTATGCCAACAAAATA... | CCATACAGTATCTGTTTCAACCACTCTCTTCTGCCGCTGTAGTGAGAAAGCAGCTATAGACACAAGAGAAATTCATTTATAAAAACAGGAAGCTGGCAGGATTTGGTCCACAGGTCATAGTTTGCAGACTCTGAGTATAGAGGAAAGAGCACAGAGAAGAATCGGAACAGAGTGGATTCCAGTTCCAGCTGTCCGTTCACCAGCTGTGCCTCTGCATCAAAACGCTCTCAGCCCTTAAATTGGGATATTTATCAGGACACTAAGGAGATAAAGGAAGGTGAAAGTGCTTGTAAATGTGTAGTTCCTATGCCAACAAAATA... |
Task1_train_42717 | A mutation on Chromosome 13 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | ATTCAATAGAAATGCTTCAGCATTGTAATCATATATATAACATTGATTCTAATAACAACATGCAATTTAACCTTGAGTGTTATAATATCAAGGTGGATTAACTGTTGTTAATCTCTTTTTCTCTTTAGTAACCATTTCAATGAAATATTATAATATCTGCTTTTCTATTAGGGAGCCCAGTGTCAATGAGTAATACTGAAATGAGTGAGTTTTTGGAGAAATAGAAGAAAAATTTTGCTCAAAACTATGGTAGTTATAAACTGGCTTGAGATTGAGGTGCGTATTTCTAAATTAATTGCAATGTTAAGCCTCAAGTGATA... | ATTCAATAGAAATGCTTCAGCATTGTAATCATATATATAACATTGATTCTAATAACAACATGCAATTTAACCTTGAGTGTTATAATATCAAGGTGGATTAACTGTTGTTAATCTCTTTTTCTCTTTAGTAACCATTTCAATGAAATATTATAATATCTGCTTTTCTATTAGGGAGCCCAGTGTCAATGAGTAATACTGAAATGAGTGAGTTTTTGGAGAAATAGAAGAAAAATTTTGCTCAAAACTATGGTAGTTATAAACTGGCTTGAGATTGAGGTGCGTATTTCTAAATTAATTGCAATGTTAAGCCTCAAGTGATA... |
Task1_train_42718 | Here is a genetic alteration on Chromosome 13. Based on the data, is it a benign variant or a cause of disease? | Benign | ACTGCTGCTTGTGCCTGTGTCAGCAGTCACAATAGTCTCTCCTTTAAGGAGGTATCTGGCTGTATTACTCATAATTTGGAAAGAATATCACATTCTGGTCCCTTGCTGAGAGGTCTGACTGTTTCAAACTCTGTTGAGAAGAAAGCAAGATTAATCCCTTCCCATTTGTTTCCCACCCTCCTCCAAACCAGACTGGAGGAGTTTATGCATATGCATTTTCAAAGAGTTGAGGATATAATTCAAAGGCACATTTCCAAATTAGCTTCTCTGGGCAGGGAACAATTAAAACTGGAGTAATTCATTTATTCTAATTGAGGTTC... | ACTGCTGCTTGTGCCTGTGTCAGCAGTCACAATAGTCTCTCCTTTAAGGAGGTATCTGGCTGTATTACTCATAATTTGGAAAGAATATCACATTCTGGTCCCTTGCTGAGAGGTCTGACTGTTTCAAACTCTGTTGAGAAGAAAGCAAGATTAATCCCTTCCCATTTGTTTCCCACCCTCCTCCAAACCAGACTGGAGGAGTTTATGCATATGCATTTTCAAAGAGTTGAGGATATAATTCAAAGGCACATTTCCAAATTAGCTTCTCTGGGCAGGGAACAATTAAAACTGGAGTAATTCATTTATTCTAATTGAGGTTC... |
Task1_train_42719 | This variant is located on Chromosome 13. Evaluate its biological effect and specify any disease association. | Benign | ATCTCCCTCCGGGCTGACATTCATTAATCAGCACCCTTTACATGTATCTATTCAACCAGATAGGGATTCCACCTTAAATATACTAGAAGCCAAACTATCTTTCTATAGTCAATAGGGAAATTATAAAAATTCTGCCAAATCTGTGCCCAGGCGCAGTGGCTCACGCCTGTAGTCCCAGCACTTTGGGAAGCCAAGGGTGGGTGGAAGGCTTGAGCCCCGGAGTTTGAGACCAGCCTGGGCAACATGGTGAAACCCCATCTCAAGAAAAAATACAAAAATTAGCCAGGCATGGTGGAGCACACCTATAGTCCCAGCTACTC... | ATCTCCCTCCGGGCTGACATTCATTAATCAGCACCCTTTACATGTATCTATTCAACCAGATAGGGATTCCACCTTAAATATACTAGAAGCCAAACTATCTTTCTATAGTCAATAGGGAAATTATAAAAATTCTGCCAAATCTGTGCCCAGGCGCAGTGGCTCACGCCTGTAGTCCCAGCACTTTGGGAAGCCAAGGGTGGGTGGAAGGCTTGAGCCCCGGAGTTTGAGACCAGCCTGGGCAACATGGTGAAACCCCATCTCAAGAAAAAATACAAAAATTAGCCAGGCATGGTGGAGCACACCTATAGTCCCAGCTACTC... |
Task1_train_42720 | Here’s a variant located on Chromosome 13. What is the predicted biological effect — harmless or disease-causing? | Benign | TTTCATAAATGATCAGATAGAGAGATGCCCTGGATTTATAATGTACAAGGCTCATCATCATATTATGTGACTAAGTTGTAGCATAACCTCTTCTAAATTATTAAATTATAGAATATATCACCAAAAGTTGTGCATGGAAAGTAAAAATTATGGAGTGTATCATTGCTTGAGGCAGGGTTAGCAGGTAGGGTGTTGAGATTAGAAGTAGACAACTCTCCTAGAGACCAATGTCCCAGTCCAAGAACCATTAAGATGAGCCCTGGAGCTACCACTTAATCATTCCTGGGTTGATTTTGATGAGAGACACAACTCCTTTGGTC... | TTTCATAAATGATCAGATAGAGAGATGCCCTGGATTTATAATGTACAAGGCTCATCATCATATTATGTGACTAAGTTGTAGCATAACCTCTTCTAAATTATTAAATTATAGAATATATCACCAAAAGTTGTGCATGGAAAGTAAAAATTATGGAGTGTATCATTGCTTGAGGCAGGGTTAGCAGGTAGGGTGTTGAGATTAGAAGTAGACAACTCTCCTAGAGACCAATGTCCCAGTCCAAGAACCATTAAGATGAGCCCTGGAGCTACCACTTAATCATTCCTGGGTTGATTTTGATGAGAGACACAACTCCTTTGGTC... |
Task1_train_42721 | Mutation context: Chromosome 13. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TAACTAACCCATTTGCCTTGTGACCTAGCACTCCCACTTCTGGGAATATGTTCTGCAACAGTATCTAACAGTATCTTTACGTGTATGAAATTGTTATTAATAGATTCATAATTTTATAGCAAAGATTATTACAATAAAATTACTTATTAAAAGATCACTGTATAAGTTTACTGTATACGTTCTAAAAGATCACTGTGTAAGTTAACTAGTCCATTATTGTGGTCTAGCCTATACTACATGTTATGGAAAATTGTCCATTATTGCAGGCTAGGTAATTAAATTGTGGACTTACGCAAAGGATTACTATACAGTCGGAGAAA... | TAACTAACCCATTTGCCTTGTGACCTAGCACTCCCACTTCTGGGAATATGTTCTGCAACAGTATCTAACAGTATCTTTACGTGTATGAAATTGTTATTAATAGATTCATAATTTTATAGCAAAGATTATTACAATAAAATTACTTATTAAAAGATCACTGTATAAGTTTACTGTATACGTTCTAAAAGATCACTGTGTAAGTTAACTAGTCCATTATTGTGGTCTAGCCTATACTACATGTTATGGAAAATTGTCCATTATTGCAGGCTAGGTAATTAAATTGTGGACTTACGCAAAGGATTACTATACAGTCGGAGAAA... |
Task1_train_42722 | Consider this mutation on Chromosome 13. Is this a benign change or a disease-causing variant? | Benign | CGCGCCGCCACACCTGACTGGTTTTCGTATTTTTTTGGTGGAGACGGGGTTTCGCTGTGTTGGCCGGGTTGGTCTCCAGCTCCTAACCGCGAGTGATCTGCCAGCCTCGGCCTCCCGAGGTGCCGAGATTGCAGACGGAGTCTCGTTCACTCAGTGCTCAATGTTGCCCAGGCTGGAGTGCAGTGGTGTGATCTCGGCTAGCTACGACCTCCACCTCCCAGCTGCCTGCCTTGGCCTCCCAAAGTGCCGAGATTGCAGCCTCTGCCCGGCCGCCACCCCGTCTGGGAAGTGAGGAGCGTCTCTGCCTGGCCGCCCATGGT... | CGCGCCGCCACACCTGACTGGTTTTCGTATTTTTTTGGTGGAGACGGGGTTTCGCTGTGTTGGCCGGGTTGGTCTCCAGCTCCTAACCGCGAGTGATCTGCCAGCCTCGGCCTCCCGAGGTGCCGAGATTGCAGACGGAGTCTCGTTCACTCAGTGCTCAATGTTGCCCAGGCTGGAGTGCAGTGGTGTGATCTCGGCTAGCTACGACCTCCACCTCCCAGCTGCCTGCCTTGGCCTCCCAAAGTGCCGAGATTGCAGCCTCTGCCCGGCCGCCACCCCGTCTGGGAAGTGAGGAGCGTCTCTGCCTGGCCGCCCATGGT... |
Task1_train_42723 | A mutation on Chromosome 13 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CCCCTGGATCTTACCAGGTATCAAAGCAGACATAATACTGAATCCCAGCCAGGGAGGGTGGCTCACACCTGTAATCCCAGCATTTTGAGAGGCCGAGGCGGGTGGATCAGTTGAGGTCAGGAGTTTGAGACCAGCTTGGCTAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAAATTAGCCAGGCGTGGTGGTGGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCATGAACCCAAGAGGCGGAGCTTGCAGTGAGCCGGGATAGCACCACTGCAGTCCAGCTTGGGCGAAAGAGTGAGA... | CCCCTGGATCTTACCAGGTATCAAAGCAGACATAATACTGAATCCCAGCCAGGGAGGGTGGCTCACACCTGTAATCCCAGCATTTTGAGAGGCCGAGGCGGGTGGATCAGTTGAGGTCAGGAGTTTGAGACCAGCTTGGCTAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAAATTAGCCAGGCGTGGTGGTGGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCATGAACCCAAGAGGCGGAGCTTGCAGTGAGCCGGGATAGCACCACTGCAGTCCAGCTTGGGCGAAAGAGTGAGA... |
Task1_train_42724 | Here is a variant on Chromosome 13. Please identify whether it is a benign mutation or associated with a disorder. | Benign | ACCAGCTTGGCTAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAAATTAGCCAGGCGTGGTGGTGGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCATGAACCCAAGAGGCGGAGCTTGCAGTGAGCCGGGATAGCACCACTGCAGTCCAGCTTGGGCGAAAGAGTGAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAACAAAAATTAGCTGGGCGTGGTGGCGCACACCTGTAGTTCCAGCTACTTGGGAGGCTGAGGCAAGAGCATCACTTGAACTGGGAGGCAGAGGTTGCAG... | ACCAGCTTGGCTAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAAATTAGCCAGGCGTGGTGGTGGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCATGAACCCAAGAGGCGGAGCTTGCAGTGAGCCGGGATAGCACCACTGCAGTCCAGCTTGGGCGAAAGAGTGAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAACAAAAATTAGCTGGGCGTGGTGGCGCACACCTGTAGTTCCAGCTACTTGGGAGGCTGAGGCAAGAGCATCACTTGAACTGGGAGGCAGAGGTTGCAG... |
Task1_train_42725 | Given this context: Chromosome 13 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AATGAGTCTGTCAGTCCTCAGCCTGCAGGACCAGCCATCTGCTGGGATCCTGGTCTGCCATGCTCCTGAACAGGTGCCTGAGATGGAGGCAGCTGGAGTAAGGGGGCAGTCAAATGAAACTGACAGGTTGTAGGTGTGGGAGGGCTCCTATCCTTGAAGATTCTGAGGCTGAGAGGGGCTTGGTCTGGGGTCATTCTGCCTGCTCTGCTGAGCAAAGCATTCACTGCTTGTAAACAAGTCTGTTGTCTGGAGTGACAGCCACACGTGGGGGTTGGTGGACATCAGACAGACCACCAGATGCTGGTGTTAGAGCCTAGCAC... | AATGAGTCTGTCAGTCCTCAGCCTGCAGGACCAGCCATCTGCTGGGATCCTGGTCTGCCATGCTCCTGAACAGGTGCCTGAGATGGAGGCAGCTGGAGTAAGGGGGCAGTCAAATGAAACTGACAGGTTGTAGGTGTGGGAGGGCTCCTATCCTTGAAGATTCTGAGGCTGAGAGGGGCTTGGTCTGGGGTCATTCTGCCTGCTCTGCTGAGCAAAGCATTCACTGCTTGTAAACAAGTCTGTTGTCTGGAGTGACAGCCACACGTGGGGGTTGGTGGACATCAGACAGACCACCAGATGCTGGTGTTAGAGCCTAGCAC... |
Task1_train_42726 | This mutation is located on Chromosome 13. Is it associated with a disease or is it a benign polymorphism? | Benign | TTGTGCAGGTTGTGCACTGCACAGTTCTCAGGGAGCATATCATGCAAGAGTATACGTAAATGTACTCCCATAGTGCTTGGGCATACATAATTAGTGCCAGCTTCTTTGTGTCCCCAGTGCCTGGTACAAACTGATTGCTTAACAGATGTGCAAATGAATGCATGAATAAGAGAGAAGACAGCAAGCTGGACTGTTTTCAAGTGAGACACTTAATAGGGTTGGGAAGAAAATTCAGACGGGTTTTGATCTGATTAAATTAAAACCATGTTATTGCAGCTGTACATGGTGAAATGGACTTGTAAGCCCACTTGGAATGTCTA... | TTGTGCAGGTTGTGCACTGCACAGTTCTCAGGGAGCATATCATGCAAGAGTATACGTAAATGTACTCCCATAGTGCTTGGGCATACATAATTAGTGCCAGCTTCTTTGTGTCCCCAGTGCCTGGTACAAACTGATTGCTTAACAGATGTGCAAATGAATGCATGAATAAGAGAGAAGACAGCAAGCTGGACTGTTTTCAAGTGAGACACTTAATAGGGTTGGGAAGAAAATTCAGACGGGTTTTGATCTGATTAAATTAAAACCATGTTATTGCAGCTGTACATGGTGAAATGGACTTGTAAGCCCACTTGGAATGTCTA... |
Task1_train_42727 | A genetic alteration is present on Chromosome 13. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | CTGGGTTGCCCCGTCCTGGTGCTGCCAGCACAGCGTCGCCCACACCCAGCATTGCTGAGGCCCATCATCCTCCTGCAGAAAAGGAGGCATGCAGTTAAATGGAGCTGGTGCTTGCTTGATAGCGCCTCCTTTTGTCAGAAAGACGCTGATGTTTCAGGCTGGCACACCCAGAAAAATCCCTTCCTTGTGGTCCTTGGCTGATGATGAGCCCTGGATCAGAGTGTCTCCAGGACCACTGAGAAGCTGCAGCCGTCTGGGTTTTCCTCTGCTATGGGGGATGAGTTACGTTTATTCCACCATGGACACCAAGAATGTATGTA... | CTGGGTTGCCCCGTCCTGGTGCTGCCAGCACAGCGTCGCCCACACCCAGCATTGCTGAGGCCCATCATCCTCCTGCAGAAAAGGAGGCATGCAGTTAAATGGAGCTGGTGCTTGCTTGATAGCGCCTCCTTTTGTCAGAAAGACGCTGATGTTTCAGGCTGGCACACCCAGAAAAATCCCTTCCTTGTGGTCCTTGGCTGATGATGAGCCCTGGATCAGAGTGTCTCCAGGACCACTGAGAAGCTGCAGCCGTCTGGGTTTTCCTCTGCTATGGGGGATGAGTTACGTTTATTCCACCATGGACACCAAGAATGTATGTA... |
Task1_train_42728 | This mutation is located on Chromosome 13. Is it associated with a disease or is it a benign polymorphism? | Benign | GACTCCAACAACCACCAAAACCCCTGCCATCCATCTTGTGACCTAGAACAATACTTAATTAAAACACCCCCCTCACTACAAGGAAGTAGGATAGGTCCTGGGAAGAGTGTTGGATTCACTGCATCTCAAAGTTGAAAGGCCCCTTGGATTGAGAAGGAGAAACTCCAAGGAGACTAAAAGCATAGTACATTAGCTCTCAATCTTTAGTGTGCACCAGAATCATCCAGAAGGCCTGTCAAACTGGATTTAACTCTTGGCCTCATTCCAGAGTTTCAGATTCTGTAGATCTGGGTGGGGAATCTAAGAATGTGCATGTCTAT... | GACTCCAACAACCACCAAAACCCCTGCCATCCATCTTGTGACCTAGAACAATACTTAATTAAAACACCCCCCTCACTACAAGGAAGTAGGATAGGTCCTGGGAAGAGTGTTGGATTCACTGCATCTCAAAGTTGAAAGGCCCCTTGGATTGAGAAGGAGAAACTCCAAGGAGACTAAAAGCATAGTACATTAGCTCTCAATCTTTAGTGTGCACCAGAATCATCCAGAAGGCCTGTCAAACTGGATTTAACTCTTGGCCTCATTCCAGAGTTTCAGATTCTGTAGATCTGGGTGGGGAATCTAAGAATGTGCATGTCTAT... |
Task1_train_42729 | A mutation on Chromosome 13 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CACACCAGCTATGTGTCTTTTCTCCTCCTCCACTCCCTGTTCCTAAACCAGAAATGGAAAAATACAGAGAAAGCCCTGAAAATTTCCCCAATAGGTCTCACGGATGATGGGTTGGTGAGATCCACTGAGTGAGGGCCGGACCCTGGCAGCTTCCTCCAGAAAGCACAAAATGGAAAACAATGCTGTCAGCATGTGCCTGCACTCCTTATCTGACAACACTGAGCTCTTTACTGCACTCTAACCACCTTCCTATGTCCAGCACTTTTTCTCATCCCTTGATTCATGTTTGTAGTTACAGGGATTGCTATGGATAATTCTGC... | CACACCAGCTATGTGTCTTTTCTCCTCCTCCACTCCCTGTTCCTAAACCAGAAATGGAAAAATACAGAGAAAGCCCTGAAAATTTCCCCAATAGGTCTCACGGATGATGGGTTGGTGAGATCCACTGAGTGAGGGCCGGACCCTGGCAGCTTCCTCCAGAAAGCACAAAATGGAAAACAATGCTGTCAGCATGTGCCTGCACTCCTTATCTGACAACACTGAGCTCTTTACTGCACTCTAACCACCTTCCTATGTCCAGCACTTTTTCTCATCCCTTGATTCATGTTTGTAGTTACAGGGATTGCTATGGATAATTCTGC... |
Task1_train_42730 | A variant affecting Chromosome 13 has been observed. Determine if it's benign or associated with disease. | Benign | ACCACCTTCCTATGTCCAGCACTTTTTCTCATCCCTTGATTCATGTTTGTAGTTACAGGGATTGCTATGGATAATTCTGCTATCTGATTCCTCAGATATATGGCAATGTTTGAAGATCTTTCTCCTTCCCTCCCTCCCTTCCTTCCCTCCCTTCCTTCCTTCCCTCCCTCTCTTTTTCTTTTCTTTTTTTCTTTTCCTTCTTTCTTCCTCCCAGCTTTTATTTTATTGTGAAATATACTGTATTGACTGGGGTACATAAAATATCCATGTACCACTTAACACATTTTTATAACAACACACATGAAACCGCCACCAAGCAA... | ACCACCTTCCTATGTCCAGCACTTTTTCTCATCCCTTGATTCATGTTTGTAGTTACAGGGATTGCTATGGATAATTCTGCTATCTGATTCCTCAGATATATGGCAATGTTTGAAGATCTTTCTCCTTCCCTCCCTCCCTTCCTTCCCTCCCTTCCTTCCTTCCCTCCCTCTCTTTTTCTTTTCTTTTTTTCTTTTCCTTCTTTCTTCCTCCCAGCTTTTATTTTATTGTGAAATATACTGTATTGACTGGGGTACATAAAATATCCATGTACCACTTAACACATTTTTATAACAACACACATGAAACCGCCACCAAGCAA... |
Task1_train_42731 | This sequence variant lies on Chromosome 13. Is it clinically significant, and what condition might it cause if any? | Benign | GGTCTTTTAATTTTCATAGAAACAGTTATATTTAGGTAGAGGGATATATTAAGATTTTTAGACATAAAGATTATGTAATCTTTTTTAAAAATACACTAATTCTTGTCAAAATCACACCTGGCATTCTGATAGGACTGGGTGGACTTCTGGAAGTTACCATGAGCCCTTCTCTACAATGACTTTTGTACAGCAGAGAGATGACAGTATCTTAAAGGAACATGCAGTACCTCATTTGCCAGCATCCTCCCTGATATTGCAGATAAAAACAAAAGAAGCCAAAGTAAGATGGAAAGGCATGGAACAGCAGAAAGCCACAGATT... | GGTCTTTTAATTTTCATAGAAACAGTTATATTTAGGTAGAGGGATATATTAAGATTTTTAGACATAAAGATTATGTAATCTTTTTTAAAAATACACTAATTCTTGTCAAAATCACACCTGGCATTCTGATAGGACTGGGTGGACTTCTGGAAGTTACCATGAGCCCTTCTCTACAATGACTTTTGTACAGCAGAGAGATGACAGTATCTTAAAGGAACATGCAGTACCTCATTTGCCAGCATCCTCCCTGATATTGCAGATAAAAACAAAAGAAGCCAAAGTAAGATGGAAAGGCATGGAACAGCAGAAAGCCACAGATT... |
Task1_train_42732 | The following genetic variant occurs on Chromosome 13. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GTGTCTTAGAAACCAAGGAAGAGAGTGTTTGGAGAAGAATGGAGAGGGCACAGATTCCGATGCTGCCCAGATGCTGGGGAAGGTAAGGCAGTCACTGGTGACCTGGGCAAGAGCAGTCTTGAGGGAGAAGTAGAAGCAAAAGTCAGACTATGAGCAAAAATCAAAAGTCAAGCACTCAGAAGTGAACAAGTAGAGTTGGTAAGTGCAAACCACACTTTCAGTAAGTTTATCTGTGAAGTACGGGGAGGGGGAGAAGAGACAGTGGCTAGGGGTGGGTGTTGCAGGACCTGAGAAAGGGCATGTGGTGCCCTAGCTTCCTA... | GTGTCTTAGAAACCAAGGAAGAGAGTGTTTGGAGAAGAATGGAGAGGGCACAGATTCCGATGCTGCCCAGATGCTGGGGAAGGTAAGGCAGTCACTGGTGACCTGGGCAAGAGCAGTCTTGAGGGAGAAGTAGAAGCAAAAGTCAGACTATGAGCAAAAATCAAAAGTCAAGCACTCAGAAGTGAACAAGTAGAGTTGGTAAGTGCAAACCACACTTTCAGTAAGTTTATCTGTGAAGTACGGGGAGGGGGAGAAGAGACAGTGGCTAGGGGTGGGTGTTGCAGGACCTGAGAAAGGGCATGTGGTGCCCTAGCTTCCTA... |
Task1_train_42733 | Consider this mutation on Chromosome 13. Is this a benign change or a disease-causing variant? | Benign | GCACAGATTCCGATGCTGCCCAGATGCTGGGGAAGGTAAGGCAGTCACTGGTGACCTGGGCAAGAGCAGTCTTGAGGGAGAAGTAGAAGCAAAAGTCAGACTATGAGCAAAAATCAAAAGTCAAGCACTCAGAAGTGAACAAGTAGAGTTGGTAAGTGCAAACCACACTTTCAGTAAGTTTATCTGTGAAGTACGGGGAGGGGGAGAAGAGACAGTGGCTAGGGGTGGGTGTTGCAGGACCTGAGAAAGGGCATGTGGTGCCCTAGCTTCCTAGCTGATAGGAAGGAGCCAGTAGAGAGGGAAAGGGTAAAAGATGCAGG... | GCACAGATTCCGATGCTGCCCAGATGCTGGGGAAGGTAAGGCAGTCACTGGTGACCTGGGCAAGAGCAGTCTTGAGGGAGAAGTAGAAGCAAAAGTCAGACTATGAGCAAAAATCAAAAGTCAAGCACTCAGAAGTGAACAAGTAGAGTTGGTAAGTGCAAACCACACTTTCAGTAAGTTTATCTGTGAAGTACGGGGAGGGGGAGAAGAGACAGTGGCTAGGGGTGGGTGTTGCAGGACCTGAGAAAGGGCATGTGGTGCCCTAGCTTCCTAGCTGATAGGAAGGAGCCAGTAGAGAGGGAAAGGGTAAAAGATGCAGG... |
Task1_train_42734 | Mutation context: Chromosome 13. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GCCAGAAATCCAGGCAGTAACATAAGCACGGCGATAGTATGCTTCACTTAGGTGATTCACTTTTTTATTTTTTCTGCTAATGTAATTTGAACTATTAAAATTGTTTTTTATATGTTTTTACTCCTTTTGTTTTTCTAATACCTGTTAATATTCTACCATCTTGCTAACATTCTCTAGTCTTCTTTTTTAATTATCTGCAATATATCTTTTTTAATAGGCTAGTCTTCCATCTACTTGTCTATTTTAACTAAGAATAAAGCAGCAGGCTGGGTGTGGTAGCTCACGCTGGTAAATCCCAGCACTTTGGGAGGCCAAGATGG... | GCCAGAAATCCAGGCAGTAACATAAGCACGGCGATAGTATGCTTCACTTAGGTGATTCACTTTTTTATTTTTTCTGCTAATGTAATTTGAACTATTAAAATTGTTTTTTATATGTTTTTACTCCTTTTGTTTTTCTAATACCTGTTAATATTCTACCATCTTGCTAACATTCTCTAGTCTTCTTTTTTAATTATCTGCAATATATCTTTTTTAATAGGCTAGTCTTCCATCTACTTGTCTATTTTAACTAAGAATAAAGCAGCAGGCTGGGTGTGGTAGCTCACGCTGGTAAATCCCAGCACTTTGGGAGGCCAAGATGG... |
Task1_train_42735 | This sequence variant lies on Chromosome 13. Is it clinically significant, and what condition might it cause if any? | Benign | CAAATTCCACTCTTTAGGCCCCACCCACTTCTTCCATAAATACCCGCTACCTGCTCATTCTGCTCATCTTGGCTCCTGTGCACCTACAGGGCTTACTCTATGATTGTTTTATACATGTGTCTCGTCATTCCAACCATTTATAAGTAGAACTGCATATGCCAGAAAGAATAGTGGTTATAATTGTATTTTTTTATTTTTTGGGACAGGGCCTCCCTCTGTTGCCCAGGCTGGAGTGCAGTGGAAAAATCACAGTTCACAGCAGCTTCAACCTCAGCCTCCCAACTCAGCCTCCTGAGTAGCTGGGACTACAAGCATTTGCC... | CAAATTCCACTCTTTAGGCCCCACCCACTTCTTCCATAAATACCCGCTACCTGCTCATTCTGCTCATCTTGGCTCCTGTGCACCTACAGGGCTTACTCTATGATTGTTTTATACATGTGTCTCGTCATTCCAACCATTTATAAGTAGAACTGCATATGCCAGAAAGAATAGTGGTTATAATTGTATTTTTTTATTTTTTGGGACAGGGCCTCCCTCTGTTGCCCAGGCTGGAGTGCAGTGGAAAAATCACAGTTCACAGCAGCTTCAACCTCAGCCTCCCAACTCAGCCTCCTGAGTAGCTGGGACTACAAGCATTTGCC... |
Task1_train_42736 | This alteration on Chromosome 13 may affect genome function. Does it lead to a disease or is it benign? | Benign | TTTCTAGTAATATATAACATCACTTTTTTTCAGAAAAATAGAAATTAATATTAACATTTACAGAAACAATATGTATGGGGTAATAATAAAAGTTATTAAATTTGGTCATTAGAGCTTGGGTTATCAGGCCACTCCATTCATGCCACATTGTTTGGAATTTATGAGTAGATCTTCTCTCTTTTTTTTTTGTTGAGACAGTCTCACTCTGTCACCCGGGCTACGGTGCAGTGGCAGGGTCTGAGCTCACTGCAACCTTCACCTCCCGAGTTCATGCGATTCTTGTGCCTCAGCCACCCAAGGAGCTGGGATTACAGGCATGG... | TTTCTAGTAATATATAACATCACTTTTTTTCAGAAAAATAGAAATTAATATTAACATTTACAGAAACAATATGTATGGGGTAATAATAAAAGTTATTAAATTTGGTCATTAGAGCTTGGGTTATCAGGCCACTCCATTCATGCCACATTGTTTGGAATTTATGAGTAGATCTTCTCTCTTTTTTTTTTGTTGAGACAGTCTCACTCTGTCACCCGGGCTACGGTGCAGTGGCAGGGTCTGAGCTCACTGCAACCTTCACCTCCCGAGTTCATGCGATTCTTGTGCCTCAGCCACCCAAGGAGCTGGGATTACAGGCATGG... |
Task1_train_42737 | This alteration on Chromosome 13 may affect genome function. Does it lead to a disease or is it benign? | Benign | CTCGGGAGGCTGAGGCAGGAGAATGGCATGAACCTGGGAGGCAGAGCTTGCAGTGAGCCGAGATGGCACCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCACCTCAAAACAAAACCACAGATATTACCTGAAGTTATCTAGCTGGCAGAAGAAATGCAGAACTAGGGTACTGAAAGATGCCAGGGGTAGAGACAGAGATTTAAGAGAGATCTACTTATTGGTAAACACTGAAGTGGGGCAGTTTAGGTGACAATGGACAGAAAAAGAAAATCAGAAAAGGACACATGGTTGAGGACATACACAGGGCGAAGACAG... | CTCGGGAGGCTGAGGCAGGAGAATGGCATGAACCTGGGAGGCAGAGCTTGCAGTGAGCCGAGATGGCACCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCACCTCAAAACAAAACCACAGATATTACCTGAAGTTATCTAGCTGGCAGAAGAAATGCAGAACTAGGGTACTGAAAGATGCCAGGGGTAGAGACAGAGATTTAAGAGAGATCTACTTATTGGTAAACACTGAAGTGGGGCAGTTTAGGTGACAATGGACAGAAAAAGAAAATCAGAAAAGGACACATGGTTGAGGACATACACAGGGCGAAGACAG... |
Task1_train_42738 | A variant on Chromosome 13 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GCTGGCAGAAGAAATGCAGAACTAGGGTACTGAAAGATGCCAGGGGTAGAGACAGAGATTTAAGAGAGATCTACTTATTGGTAAACACTGAAGTGGGGCAGTTTAGGTGACAATGGACAGAAAAAGAAAATCAGAAAAGGACACATGGTTGAGGACATACACAGGGCGAAGACAGAGATAAGCCTGAGGGAGAGCAGTCAGATAAACAAAAGAGAGTGAGCAGAATAATGTCATGGGAGGAAGCTATTGCGGGCCACTAGAATAAGAGGACATTATTATGAATATGCCATGGATTCACAAAAAGAGACCTATATTGGGAA... | GCTGGCAGAAGAAATGCAGAACTAGGGTACTGAAAGATGCCAGGGGTAGAGACAGAGATTTAAGAGAGATCTACTTATTGGTAAACACTGAAGTGGGGCAGTTTAGGTGACAATGGACAGAAAAAGAAAATCAGAAAAGGACACATGGTTGAGGACATACACAGGGCGAAGACAGAGATAAGCCTGAGGGAGAGCAGTCAGATAAACAAAAGAGAGTGAGCAGAATAATGTCATGGGAGGAAGCTATTGCGGGCCACTAGAATAAGAGGACATTATTATGAATATGCCATGGATTCACAAAAAGAGACCTATATTGGGAA... |
Task1_train_42739 | A mutation found on Chromosome 13 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | ATCTTGACTCTCTGTAGCCCTAACATAATCTAGTCATCAACTCCTGAATAAGACATGGCTGTCAGTACTTGGCCTCTCCACACCAAATCATTGACTCAAGATTGTTTATTAAAGAAGGACCTGTGATGCTGTTGTCATTGTCCTTAACCTGTAAACTTGCTGCCTTCCTCACTTTCCATTTATTCTTTAACCCTCTGTAGTATTGCATTTGACTTATTACCCTGAATTTGTTGTTACAAAGGTCACTAAGAGTAACCAATTTCCATATTGCTGAATCCCATCCTTCCTTCTCTTCCTGGACCTCTTGATCAATTGATAAC... | ATCTTGACTCTCTGTAGCCCTAACATAATCTAGTCATCAACTCCTGAATAAGACATGGCTGTCAGTACTTGGCCTCTCCACACCAAATCATTGACTCAAGATTGTTTATTAAAGAAGGACCTGTGATGCTGTTGTCATTGTCCTTAACCTGTAAACTTGCTGCCTTCCTCACTTTCCATTTATTCTTTAACCCTCTGTAGTATTGCATTTGACTTATTACCCTGAATTTGTTGTTACAAAGGTCACTAAGAGTAACCAATTTCCATATTGCTGAATCCCATCCTTCCTTCTCTTCCTGGACCTCTTGATCAATTGATAAC... |
Task1_train_42740 | Chromosome 13 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GAATTTGTTGTTACAAAGGTCACTAAGAGTAACCAATTTCCATATTGCTGAATCCCATCCTTCCTTCTCTTCCTGGACCTCTTGATCAATTGATAACCTTTCATAACTCACTTTTCCTCTAAACTCTCTATTGCCTTCAGTTTTGCCCAATCTGAAGTGCCCAACTGTCCTATCCTGCTTCTGTAATATTTTCCCCCTTTTACCATGTAAAAAATAATTTCCTGATGTTCCCTTTGGGTTGCTCCAGAGACTTTTTCAAAGATTGGAGTTCTCCCAAGTTTTGTCTAAAGGTCACTGTTCTTATTCTCTGTTTTCAACTT... | GAATTTGTTGTTACAAAGGTCACTAAGAGTAACCAATTTCCATATTGCTGAATCCCATCCTTCCTTCTCTTCCTGGACCTCTTGATCAATTGATAACCTTTCATAACTCACTTTTCCTCTAAACTCTCTATTGCCTTCAGTTTTGCCCAATCTGAAGTGCCCAACTGTCCTATCCTGCTTCTGTAATATTTTCCCCCTTTTACCATGTAAAAAATAATTTCCTGATGTTCCCTTTGGGTTGCTCCAGAGACTTTTTCAAAGATTGGAGTTCTCCCAAGTTTTGTCTAAAGGTCACTGTTCTTATTCTCTGTTTTCAACTT... |
Task1_train_42741 | Given a variant located on Chromosome 13, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TGTGTACATAATATGTGTAATTCTTGTATGGATGTTGTGGTGATTGAATACTTAAAATGTGGTCACGCTATTGGGCTGGGAGGGAACAAGCCACATCTTGGATATGTAGGGAAGAAGCTCTTTCCCCAAGTGAGAAATTACTCATCCTATCAGTTGTCTTAGCATTGCCAATAATGCTGTGTTCCGATCTCTAGTGCCCACCCCATGGCCCTGCACTGGCATTTTCCATAGCACCTTGTATCATATTATACAATTTTCTTATTTTAATTTAGTGTTTATTTACTGTCTCCCCTTGCTGCAATGCAAAACTCCCTGAGGGC... | TGTGTACATAATATGTGTAATTCTTGTATGGATGTTGTGGTGATTGAATACTTAAAATGTGGTCACGCTATTGGGCTGGGAGGGAACAAGCCACATCTTGGATATGTAGGGAAGAAGCTCTTTCCCCAAGTGAGAAATTACTCATCCTATCAGTTGTCTTAGCATTGCCAATAATGCTGTGTTCCGATCTCTAGTGCCCACCCCATGGCCCTGCACTGGCATTTTCCATAGCACCTTGTATCATATTATACAATTTTCTTATTTTAATTTAGTGTTTATTTACTGTCTCCCCTTGCTGCAATGCAAAACTCCCTGAGGGC... |
Task1_train_42742 | Consider this mutation on Chromosome 13. Is this a benign change or a disease-causing variant? | Benign | GTAATTCCAACATGTTTTGTTTTTTGTCTTACAGACAGTTCCTTTGGCAATAACTTCCACTTTAGCTTTTATTATATAAAAATATAACAAAATTTCATTATATACAAACATTACATTACACAATGTACAGGTTAAAAACACTAAGAAAATGGCAAGCCGCAATTGAAATCAAAGTCAATAGCATAAGAAAAATTAAATACTGCACACATTTCATAAAAATTACATTAACTACATTTTTGTTTGCAAATACCAAACAGTACCAATGTGATTGGAAATAGCTTCCAACAACTTCATTGTAAGGCACATCTTGCATATTTATA... | GTAATTCCAACATGTTTTGTTTTTTGTCTTACAGACAGTTCCTTTGGCAATAACTTCCACTTTAGCTTTTATTATATAAAAATATAACAAAATTTCATTATATACAAACATTACATTACACAATGTACAGGTTAAAAACACTAAGAAAATGGCAAGCCGCAATTGAAATCAAAGTCAATAGCATAAGAAAAATTAAATACTGCACACATTTCATAAAAATTACATTAACTACATTTTTGTTTGCAAATACCAAACAGTACCAATGTGATTGGAAATAGCTTCCAACAACTTCATTGTAAGGCACATCTTGCATATTTATA... |
Task1_train_42743 | This is a variant located on Chromosome 13. Is this mutation a likely cause of disease or not? | Benign | TATCCGCAGCTGTAGGAGTGAGAAAAAGTGGGGAAGAGGGAAGGGGGCTGGGAACCGAGATTGAGAGGAGGCAAACAGTGGTGAAGGGGAGGGAAGGGAGGAATGCCGAATTTGGCGGGAAAGAAGAGTCCTCACCACTCTGCATGTGGTTGATGAGATCCTTTTTCAGAGCGTCCCCGCTGATGTCGGAATCGCTGTCGTTGAAATCACTGTCCCCTTTACCGCTGTCTTTGCCGCTGAACTTCTCTGCTTCTCTGCCAGAAATGGTGTTGAAGGAGTGTCCTTTCCACACCGCCACAGGGGGCGCCGGCTCCTTTCCA... | TATCCGCAGCTGTAGGAGTGAGAAAAAGTGGGGAAGAGGGAAGGGGGCTGGGAACCGAGATTGAGAGGAGGCAAACAGTGGTGAAGGGGAGGGAAGGGAGGAATGCCGAATTTGGCGGGAAAGAAGAGTCCTCACCACTCTGCATGTGGTTGATGAGATCCTTTTTCAGAGCGTCCCCGCTGATGTCGGAATCGCTGTCGTTGAAATCACTGTCCCCTTTACCGCTGTCTTTGCCGCTGAACTTCTCTGCTTCTCTGCCAGAAATGGTGTTGAAGGAGTGTCCTTTCCACACCGCCACAGGGGGCGCCGGCTCCTTTCCA... |
Task1_train_42744 | This mutation occurs on Chromosome 13. Does this change lead to a known medical condition, or is it benign? | Benign | AAGAGGGGAATTGTGCTGGGAGGTAGAGACACATTCTTCTCCTTATGTCCATATTCATTGCATTCAATCTTAGAATAATGGATTCAGTCTCCCAGTTTTCATTCTCACACATTCTGTATGCATTCCCTGCCTTGGACTGGGGATCTAAGTGGTTAGAACATTTGACCAAAGAGGCCAAGGCTGAACTGCTTCCCACAGAGAACAATGAACTTTACAGCCCACATTTCTCCCTATCTGTTCTTCTTCACTCTCTATCCATCCATTTGTGGTTTTCCTGTCTCCCCTTCCCCCTCCCCACCACCCCAGTTTCTGAATAGTGT... | AAGAGGGGAATTGTGCTGGGAGGTAGAGACACATTCTTCTCCTTATGTCCATATTCATTGCATTCAATCTTAGAATAATGGATTCAGTCTCCCAGTTTTCATTCTCACACATTCTGTATGCATTCCCTGCCTTGGACTGGGGATCTAAGTGGTTAGAACATTTGACCAAAGAGGCCAAGGCTGAACTGCTTCCCACAGAGAACAATGAACTTTACAGCCCACATTTCTCCCTATCTGTTCTTCTTCACTCTCTATCCATCCATTTGTGGTTTTCCTGTCTCCCCTTCCCCCTCCCCACCACCCCAGTTTCTGAATAGTGT... |
Task1_train_42745 | The following genetic variant occurs on Chromosome 13. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | AGCTCAGCTTCCACCATAAAACAGTAATAGAAATGGAAAGTAGATATAGAGAACATTTACTAAGCATACACCATATGCCAAGGGTTTGGCTAGAACTTTTACCCACATTCCCATATTTCATCTGCCTAACAACCCAGTGAGTTAGGCACTAATCTCCATATTTAGTCACATTATAATGTAGATGAGGTTAAAAGAAAGATAAATAATTTGTTAACCTCAGATGGCTAGGATATAATCAATCTTTAAAAGCCATTTGTCTGGCTTTTTGATATATTAGCAACATTAAACGCAACTGTATTATTAAGACTTGCCAGCTACTT... | AGCTCAGCTTCCACCATAAAACAGTAATAGAAATGGAAAGTAGATATAGAGAACATTTACTAAGCATACACCATATGCCAAGGGTTTGGCTAGAACTTTTACCCACATTCCCATATTTCATCTGCCTAACAACCCAGTGAGTTAGGCACTAATCTCCATATTTAGTCACATTATAATGTAGATGAGGTTAAAAGAAAGATAAATAATTTGTTAACCTCAGATGGCTAGGATATAATCAATCTTTAAAAGCCATTTGTCTGGCTTTTTGATATATTAGCAACATTAAACGCAACTGTATTATTAAGACTTGCCAGCTACTT... |
Task1_train_42746 | Given a variant located on Chromosome 13, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CCTTAGATGCTTGTGGAACTTTCTGACTGTAAGAATAAGTAATTTGAGCATTGGTCCCCAAGTCTTTATCCACAGCCTGGACAGCTGCAATTGGGGTGCCCACTGTAGCATTCCCATACACAGTGACATTGATTTGTGAGTCTGTGAAGAGAGGGCAATTGTCATTAATGTCACTGATGCCAATGGTGAGAGTGGCACTGCCCAAAAGTGGTGGAGACCCACCATCCTCAGCTATGATGATGCTCACATACTGGTCCTGGGTTTCCCTGTCCAAAGCACCCATGACAATTAGGTAGGGGGTGCGCTCCCCATTCTCATTC... | CCTTAGATGCTTGTGGAACTTTCTGACTGTAAGAATAAGTAATTTGAGCATTGGTCCCCAAGTCTTTATCCACAGCCTGGACAGCTGCAATTGGGGTGCCCACTGTAGCATTCCCATACACAGTGACATTGATTTGTGAGTCTGTGAAGAGAGGGCAATTGTCATTAATGTCACTGATGCCAATGGTGAGAGTGGCACTGCCCAAAAGTGGTGGAGACCCACCATCCTCAGCTATGATGATGCTCACATACTGGTCCTGGGTTTCCCTGTCCAAAGCACCCATGACAATTAGGTAGGGGGTGCGCTCCCCATTCTCATTC... |
Task1_train_42747 | A mutation on Chromosome 13 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | ACAGTGGAATGTAAGTCCTAGGAAAGGAAATTGTTTTTACTTAGCTCAGTGCTTTATCTCCAGTGCCTAGAACAGTATCTAGCACGTGGTAGGTATTCAATAAATATTTTTTGACTGAGCGAATTTTTAAAATTGTGTTTTTATTAACCTGCTGTTTAGAAGACCAATAACAAAGCCTTAACTGAAGTAATTGTATGAAGCTGTAATTGTGGAGTTTGAAATCAGACTAAAGACTGTGGGATGCGGGTGGGGTGCATTTCAAGAGAATTCATCATTCTGATTTCCCCATAAATTACTCATCATATGAAGTGGCCAATAAT... | ACAGTGGAATGTAAGTCCTAGGAAAGGAAATTGTTTTTACTTAGCTCAGTGCTTTATCTCCAGTGCCTAGAACAGTATCTAGCACGTGGTAGGTATTCAATAAATATTTTTTGACTGAGCGAATTTTTAAAATTGTGTTTTTATTAACCTGCTGTTTAGAAGACCAATAACAAAGCCTTAACTGAAGTAATTGTATGAAGCTGTAATTGTGGAGTTTGAAATCAGACTAAAGACTGTGGGATGCGGGTGGGGTGCATTTCAAGAGAATTCATCATTCTGATTTCCCCATAAATTACTCATCATATGAAGTGGCCAATAAT... |
Task1_train_42748 | Consider this mutation on Chromosome 13. Is this a benign change or a disease-causing variant? | Benign | TGCTTCCTTGACAATGAGTATCAGTTACTCAAAGAAGTATTTTTATAGTTTCCTGAAATGTCTTTTGTAAGGGCTTTTAAACTTTATTGTATGTTTGAGCTTATTTCACATAATGATCATGATTATAAAACAAACTGGCATAGTTTGCCTTAATATTTAATTATGCAAATAAACTATGAAACACCTTCAATAAAAGTATCAATTATAAAAACATCAATTAAAGAAATAAATTCATTGCTTGACTCTAAGATCTGAATAAAACTTTTTCTTTACAAGAAGCACACTGGACTTGCGATTTGTATACATATCTTATTCTATAG... | TGCTTCCTTGACAATGAGTATCAGTTACTCAAAGAAGTATTTTTATAGTTTCCTGAAATGTCTTTTGTAAGGGCTTTTAAACTTTATTGTATGTTTGAGCTTATTTCACATAATGATCATGATTATAAAACAAACTGGCATAGTTTGCCTTAATATTTAATTATGCAAATAAACTATGAAACACCTTCAATAAAAGTATCAATTATAAAAACATCAATTAAAGAAATAAATTCATTGCTTGACTCTAAGATCTGAATAAAACTTTTTCTTTACAAGAAGCACACTGGACTTGCGATTTGTATACATATCTTATTCTATAG... |
Task1_train_42749 | A variant on Chromosome 13 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | AAAATTTTATTTTTGATCTCACGGGTTGATTTAAATACTGTGTAACACCACATCCCCTCTCCTTCATTTTTTGTTTTACTTCACTTTTTTGTGTTCTTACTCTCTTTATAATCTTCATTTCACACCAAGTTTTCTCAGAAGAGATCTTGATGATGCAGCCAACACAAACCATCAGTTCTCAATTGTACATCAGTGATTCCACCAGAGAAAATGTGAGTTTTCTGTTCAAATGGGATCCTGTGGCCATATACATAAGGAACCTAAGTACAGCTAACCTAAGAAAATAGGCTAGAAGTGAGGTCTTATACTCTACCTTTTTC... | AAAATTTTATTTTTGATCTCACGGGTTGATTTAAATACTGTGTAACACCACATCCCCTCTCCTTCATTTTTTGTTTTACTTCACTTTTTTGTGTTCTTACTCTCTTTATAATCTTCATTTCACACCAAGTTTTCTCAGAAGAGATCTTGATGATGCAGCCAACACAAACCATCAGTTCTCAATTGTACATCAGTGATTCCACCAGAGAAAATGTGAGTTTTCTGTTCAAATGGGATCCTGTGGCCATATACATAAGGAACCTAAGTACAGCTAACCTAAGAAAATAGGCTAGAAGTGAGGTCTTATACTCTACCTTTTTC... |
Task1_train_42750 | This mutation on Chromosome 13 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TCTTTGAAAAGAAAACCAGGACCAGTGCAGAAAAAGCCAGCAGCCCCTCTGCAAGTGCTACATAAGAAAATGAGGCCGGGCATGGTGGCTCACGCCTGTAATCCTAGCATTTTGGGAGGCCGAGGCATGTGGATCACCTGAAGTCAGGAGTTCGAGACCAACCTGGCCAACATGGGGAAACTCCGTCTCTACTAAAAATACAAAAAATTAGCCGGGTGTTCTGGCGGGCACCTGTAATCCCAGCTACTCCAGAGGCTGAGGCAGGAGAATCGCCTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCGAGGTTGCGCCATTG... | TCTTTGAAAAGAAAACCAGGACCAGTGCAGAAAAAGCCAGCAGCCCCTCTGCAAGTGCTACATAAGAAAATGAGGCCGGGCATGGTGGCTCACGCCTGTAATCCTAGCATTTTGGGAGGCCGAGGCATGTGGATCACCTGAAGTCAGGAGTTCGAGACCAACCTGGCCAACATGGGGAAACTCCGTCTCTACTAAAAATACAAAAAATTAGCCGGGTGTTCTGGCGGGCACCTGTAATCCCAGCTACTCCAGAGGCTGAGGCAGGAGAATCGCCTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCGAGGTTGCGCCATTG... |
Task1_train_42751 | Given a variant located on Chromosome 13, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AAAAACTTACATAAAAGAGGCCAGGCACATTGGCTCATGCCTGTAATCTCAGCATTTTGGGAGGCTGAGGTGGGTGGATCACTTGAGGCCAGTTCAAGACCAGCCTGGCCAACACAGCGAAACCCTATGTCTACTAAAAATTAGCTGGGCACGGTAGTGCACGCCTGTAGTCCCAGCTAATCGGGAGGCTGAGACACAAGAATCGCTTGAACCTGGGAGGCTGAGGGTGCAGTGGGCCGAAATCACAGAACTGCACTCCAGCCGGGGCAACAGGGTGAGACTCTCTCTCAAAAAGAAGAAATTTACATAAAAGTAACCAA... | AAAAACTTACATAAAAGAGGCCAGGCACATTGGCTCATGCCTGTAATCTCAGCATTTTGGGAGGCTGAGGTGGGTGGATCACTTGAGGCCAGTTCAAGACCAGCCTGGCCAACACAGCGAAACCCTATGTCTACTAAAAATTAGCTGGGCACGGTAGTGCACGCCTGTAGTCCCAGCTAATCGGGAGGCTGAGACACAAGAATCGCTTGAACCTGGGAGGCTGAGGGTGCAGTGGGCCGAAATCACAGAACTGCACTCCAGCCGGGGCAACAGGGTGAGACTCTCTCTCAAAAAGAAGAAATTTACATAAAAGTAACCAA... |
Task1_train_42752 | Consider a variant on Chromosome 13. Determine its clinical classification and disease relevance. | Benign | TTCTATTAAATGTTTATCATTTTTTTATTACATAGTAAATGCTCTTTACTCACCTCCTTAATGTCAGACTTGGAAAGCATGCCACAATATGGTCTCCAATTCCTTTTTATTATTCCTACAACTCTACCTGTAGGCTTCAACATTTTCTCGCTTACAGCAGTCTTAAGCTGAGATATAAAAATTAAAATGTTCAGTTATATTCCTCTAAGTATTATCAGGCAATTTCCTTTCAAAATCAAAATGCATACATGGATACTAATCCATTCAGGCAGTAAATTATGACATAAGACTACAGAATGTTGATGTTTCAACATTCTAGA... | TTCTATTAAATGTTTATCATTTTTTTATTACATAGTAAATGCTCTTTACTCACCTCCTTAATGTCAGACTTGGAAAGCATGCCACAATATGGTCTCCAATTCCTTTTTATTATTCCTACAACTCTACCTGTAGGCTTCAACATTTTCTCGCTTACAGCAGTCTTAAGCTGAGATATAAAAATTAAAATGTTCAGTTATATTCCTCTAAGTATTATCAGGCAATTTCCTTTCAAAATCAAAATGCATACATGGATACTAATCCATTCAGGCAGTAAATTATGACATAAGACTACAGAATGTTGATGTTTCAACATTCTAGA... |
Task1_train_42753 | Chromosome 13 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GAGTTTCTGACTTGTGGGGGTGGGGTCCTGAGAATGTGCATTTTTACTGGGTTCGCAGGTGATGCAGATGCTGCTGGTCCAGAAACAATACTTTGAGAACCACTGCATTTGATAATAGGTCTTCTATGCTAATTCTGTAAGACATATATCAGATTGAATGATGCTGCTGAGAGGGCAGTCACGAGTCTATTGTAATAAAACTCTTGATAGCTGATGGTCATAAAAAATGGTTGGATTCTGAATATTTTTTGGAGGGCTGATGGATTCAATGTGGGGCTTAAGAGAAAAAGGGGAGTCAAGGATTACATCAAAAGTTTTGG... | GAGTTTCTGACTTGTGGGGGTGGGGTCCTGAGAATGTGCATTTTTACTGGGTTCGCAGGTGATGCAGATGCTGCTGGTCCAGAAACAATACTTTGAGAACCACTGCATTTGATAATAGGTCTTCTATGCTAATTCTGTAAGACATATATCAGATTGAATGATGCTGCTGAGAGGGCAGTCACGAGTCTATTGTAATAAAACTCTTGATAGCTGATGGTCATAAAAAATGGTTGGATTCTGAATATTTTTTGGAGGGCTGATGGATTCAATGTGGGGCTTAAGAGAAAAAGGGGAGTCAAGGATTACATCAAAAGTTTTGG... |
Task1_train_42754 | This variant is present on Chromosome 13. Is the change likely to result in a pathogenic outcome? | Benign | ATACTTTATATTTTTAATTATAAATCAGGTTCCACAATAGTATATATAGTATGATTTCATTTATGTACAACTTTATATATTTTTATATGTATATATAAGCAAAGAAACATGTAATACAAAGTTTCAAAGATTATCTCTAGATGTTGAGATTTATAGTTACTTTTATTTTCTTGTGATTTTCTGCATTATTTGCATTTTTTTCCAGTGTCCATAAATAAAGTTCATCAAAGTCTCCCTTAATATCAGCATTTCATTCCACAGTAATCAACTCTAATTGTTAGTAAATTCTCTCCAATATCAAGTTCAAATTTACCTGCCTA... | ATACTTTATATTTTTAATTATAAATCAGGTTCCACAATAGTATATATAGTATGATTTCATTTATGTACAACTTTATATATTTTTATATGTATATATAAGCAAAGAAACATGTAATACAAAGTTTCAAAGATTATCTCTAGATGTTGAGATTTATAGTTACTTTTATTTTCTTGTGATTTTCTGCATTATTTGCATTTTTTTCCAGTGTCCATAAATAAAGTTCATCAAAGTCTCCCTTAATATCAGCATTTCATTCCACAGTAATCAACTCTAATTGTTAGTAAATTCTCTCCAATATCAAGTTCAAATTTACCTGCCTA... |
Task1_train_42755 | A mutation on Chromosome 13 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CTGCTTATGTGCCAGCCGCACACCCTGAGGATAAAATGGTGAACAGGGACAGTTAATATCTGCCCTTAACTGTTTAACTAGAAAAGACTAAAGAACTATCAAGAAATAATTATCCATTGGTTAGAATTTTCATAGGTTAAACTATTTTTTATCTTTGTTATGTAGGCAGAGAAACAGAGAACCGATGAAGGTTTCTGAGAATGTATTCTAAATGTCACCTCCTTTCTTAACCTGTAAAATCATATAGTATAACTGATCTCAGAATACACAGCAGCCATTTATGTAAAACATTCCATTTCCTTATATTAACATACACAGCT... | CTGCTTATGTGCCAGCCGCACACCCTGAGGATAAAATGGTGAACAGGGACAGTTAATATCTGCCCTTAACTGTTTAACTAGAAAAGACTAAAGAACTATCAAGAAATAATTATCCATTGGTTAGAATTTTCATAGGTTAAACTATTTTTTATCTTTGTTATGTAGGCAGAGAAACAGAGAACCGATGAAGGTTTCTGAGAATGTATTCTAAATGTCACCTCCTTTCTTAACCTGTAAAATCATATAGTATAACTGATCTCAGAATACACAGCAGCCATTTATGTAAAACATTCCATTTCCTTATATTAACATACACAGCT... |
Task1_train_42756 | Chromosome 13 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | ATATTTATATAGTTCAGCCTCTAACGCTTAAATATATAATGGAGGAAAATAAAGGAATGTTTATAATTGACTTCCTACCAATGAGACCAAGAGGAACTCAACAGCAGCTGTTGAGAACTAAAGGTGCCAGGACCATCAATGAGATTAGCAACAATGTGTCATGCATCAGATGTCGCTGGGGGGAAATAACTTTAACAGAAACCCCCGAGAGTCATGAAAAGTTCCTTAAAGTCCTGGAAAAATGCAACTGGCTCCTCTTTACCACCAGAACCAGAAAAATGTAATACAATAAAATGTAATAGCTTTCAGAAACTTTCCAA... | ATATTTATATAGTTCAGCCTCTAACGCTTAAATATATAATGGAGGAAAATAAAGGAATGTTTATAATTGACTTCCTACCAATGAGACCAAGAGGAACTCAACAGCAGCTGTTGAGAACTAAAGGTGCCAGGACCATCAATGAGATTAGCAACAATGTGTCATGCATCAGATGTCGCTGGGGGGAAATAACTTTAACAGAAACCCCCGAGAGTCATGAAAAGTTCCTTAAAGTCCTGGAAAAATGCAACTGGCTCCTCTTTACCACCAGAACCAGAAAAATGTAATACAATAAAATGTAATAGCTTTCAGAAACTTTCCAA... |
Task1_train_42757 | This mutation on Chromosome 13 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GCTTCTCCCTGCGGAAAAATGCCCTGTACTATCTCATTATAAGGTCATGATACGTGAACACTTAGTTATCTCCCTGAATGAAAAATTATGGCAAACATGGCTCTTGGGAATTGTTTCATGATGTGGTTCGTCTGTACCACAGTGGTTTCTAACGTAAATGTTTGTTGGGATATTTTTGTTTCTCATTACTAATGTTGAAATGATTGGTGTGATGATGGTTTGTATCTTAAGTATCATGACCTAGTAGCTGATCTGTCAATTAGTAAGTAACTTAATTTGGAATCAACTGTGAGCCCAGTTGAAGCTCACAGCCTAATGTT... | GCTTCTCCCTGCGGAAAAATGCCCTGTACTATCTCATTATAAGGTCATGATACGTGAACACTTAGTTATCTCCCTGAATGAAAAATTATGGCAAACATGGCTCTTGGGAATTGTTTCATGATGTGGTTCGTCTGTACCACAGTGGTTTCTAACGTAAATGTTTGTTGGGATATTTTTGTTTCTCATTACTAATGTTGAAATGATTGGTGTGATGATGGTTTGTATCTTAAGTATCATGACCTAGTAGCTGATCTGTCAATTAGTAAGTAACTTAATTTGGAATCAACTGTGAGCCCAGTTGAAGCTCACAGCCTAATGTT... |
Task1_train_42758 | The following genetic variant occurs on Chromosome 13. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TTAAATTTAAACCTGAGGATCTAGATCTTAAAAAGCCCTGTTCTATACATAGTCATAGCACGGCATTATTTTTAGTAGTTCTGTTTTTCTCCAATTCTTTGTCTCATTCCCTCTTCCCTTCTTTTCTTCATGTCACTCACAGTAGAAGGAATTCAGACTCTGAGGATGAGGACTCAGGTTCTGACAGAAGCGCCACCGTTTTTAGTAGAGCACAAAAAGCAGAGCATAGGCTAGACGGCAACTGCCAAAGACCTTCACTCTTGCTGGAATTAGCTACCAAACGGGCTGTAAAATCACCGGACTCCCATGCAGCCAGGAGA... | TTAAATTTAAACCTGAGGATCTAGATCTTAAAAAGCCCTGTTCTATACATAGTCATAGCACGGCATTATTTTTAGTAGTTCTGTTTTTCTCCAATTCTTTGTCTCATTCCCTCTTCCCTTCTTTTCTTCATGTCACTCACAGTAGAAGGAATTCAGACTCTGAGGATGAGGACTCAGGTTCTGACAGAAGCGCCACCGTTTTTAGTAGAGCACAAAAAGCAGAGCATAGGCTAGACGGCAACTGCCAAAGACCTTCACTCTTGCTGGAATTAGCTACCAAACGGGCTGTAAAATCACCGGACTCCCATGCAGCCAGGAGA... |
Task1_train_42759 | A change on Chromosome 13 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CAGTTGGAGTGAATAGTTTCAGTGATGTAATAAGATACTCTGGCACATTCTGTCTGCTAGAAAGGGTGTATAGAAATTCAGGTGTGCCCCTGCTGATGTGATTTTTCTGTCAGGACCTTGCAAAATGGAAAGATCGTCGAAAAAGTTACACTTCAGATCTGCAGAAGAAAAAAGAAGAGAGAGAAGAAATTGAAAAGCAGGCACTTGAGAAGTCTAAGAGAAGCTCTAAGACGTTTAAGGAAATGCTGCAGGACAGGTAATAATGCTGAATGCACCTCGGTTGTAACAGGGTTGGAGATGCCAGTGTTATAAATAGATAT... | CAGTTGGAGTGAATAGTTTCAGTGATGTAATAAGATACTCTGGCACATTCTGTCTGCTAGAAAGGGTGTATAGAAATTCAGGTGTGCCCCTGCTGATGTGATTTTTCTGTCAGGACCTTGCAAAATGGAAAGATCGTCGAAAAAGTTACACTTCAGATCTGCAGAAGAAAAAAGAAGAGAGAGAAGAAATTGAAAAGCAGGCACTTGAGAAGTCTAAGAGAAGCTCTAAGACGTTTAAGGAAATGCTGCAGGACAGGTAATAATGCTGAATGCACCTCGGTTGTAACAGGGTTGGAGATGCCAGTGTTATAAATAGATAT... |
Task1_train_42760 | An alteration has been detected on Chromosome 13. Is it pathogenic, and if so, what disease is involved? | Benign | ATCTGCAGAAGAAAAAAGAAGAGAGAGAAGAAATTGAAAAGCAGGCACTTGAGAAGTCTAAGAGAAGCTCTAAGACGTTTAAGGAAATGCTGCAGGACAGGTAATAATGCTGAATGCACCTCGGTTGTAACAGGGTTGGAGATGCCAGTGTTATAAATAGATATTTTATGTAAGTGTAGTGTGACATAGGTGTCCACCAATATTCAACTTTAGTCAAATATGCAAAGAAACGTTTAAGATTTTGGTCTGCGGTGAAAAAACAAAGCATTGTTGAAATAGTGACTTAGAGTAATAGTAACAAAATAAATGAGGACTTAAAA... | ATCTGCAGAAGAAAAAAGAAGAGAGAGAAGAAATTGAAAAGCAGGCACTTGAGAAGTCTAAGAGAAGCTCTAAGACGTTTAAGGAAATGCTGCAGGACAGGTAATAATGCTGAATGCACCTCGGTTGTAACAGGGTTGGAGATGCCAGTGTTATAAATAGATATTTTATGTAAGTGTAGTGTGACATAGGTGTCCACCAATATTCAACTTTAGTCAAATATGCAAAGAAACGTTTAAGATTTTGGTCTGCGGTGAAAAAACAAAGCATTGTTGAAATAGTGACTTAGAGTAATAGTAACAAAATAAATGAGGACTTAAAA... |
Task1_train_42761 | A mutation found on Chromosome 13 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GTCACACCAAGACCCTTTGGCTCTCAGACAAGGGGAATCTCATCACTCCCCAGATCTTACACGGTAAAAAATGTTCTCGGTTCATTTAGTCTGTTCTGAAGAGCAAAATGTTGGTGAACTTGTGCAGAGGTTGGGGTTACATCAACTTGATGTGTAAACTGTACATAACATATATAAGGACATTTTATTTTATGCCAGTTTAGATGCAATGGAAACTTAATGCTTAAGATATATCAATGATACAGAATTTATTAAACTTTAAATTCTGTGAAAGTAGGGCTGATACATTTTAAAGAATGAATAAGATATATTCTAAGGCA... | GTCACACCAAGACCCTTTGGCTCTCAGACAAGGGGAATCTCATCACTCCCCAGATCTTACACGGTAAAAAATGTTCTCGGTTCATTTAGTCTGTTCTGAAGAGCAAAATGTTGGTGAACTTGTGCAGAGGTTGGGGTTACATCAACTTGATGTGTAAACTGTACATAACATATATAAGGACATTTTATTTTATGCCAGTTTAGATGCAATGGAAACTTAATGCTTAAGATATATCAATGATACAGAATTTATTAAACTTTAAATTCTGTGAAAGTAGGGCTGATACATTTTAAAGAATGAATAAGATATATTCTAAGGCA... |
Task1_train_42762 | This variant lies on Chromosome 13. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AGTCTGACCAAATTGATAAGCTTTGTATGTACACAAATGTAAGTATAGTTGTATAAGAAACCTTTGGTCTTGCTCATTGCTTAGTGGAAGATGAACCAAGGCATAGACAAACAATAAATTTTGAAAGAATGGCAGTAGCAATAAATGTAGAGAAAGAAAATAAATCCTTAGATGCAATTTCCTAATCCAGATTAAGGTGGGAATGATACGTCAAAGTTGTGGGTGTTTTACCCCAATCAGAAACTAATCGCCAAATCCAAGAGACAGAGTCCTCACGATAAAACCTGACTTAATTGTCATGAATAAATTCAACATTCAAA... | AGTCTGACCAAATTGATAAGCTTTGTATGTACACAAATGTAAGTATAGTTGTATAAGAAACCTTTGGTCTTGCTCATTGCTTAGTGGAAGATGAACCAAGGCATAGACAAACAATAAATTTTGAAAGAATGGCAGTAGCAATAAATGTAGAGAAAGAAAATAAATCCTTAGATGCAATTTCCTAATCCAGATTAAGGTGGGAATGATACGTCAAAGTTGTGGGTGTTTTACCCCAATCAGAAACTAATCGCCAAATCCAAGAGACAGAGTCCTCACGATAAAACCTGACTTAATTGTCATGAATAAATTCAACATTCAAA... |
Task1_train_42763 | This variant is located on Chromosome 13. Evaluate its biological effect and specify any disease association. | Benign | ATGAGCAGAATGACGATAGTTCTAAGATAATACATATTAAATGGAAAAGAAGTTATTGAAAACTGTGTTGTGGAATAATCCATTTGTTTAAGACTGTTAAACACAAGCACATTGCATATGTATATAGACACATCTATACTTACATATGTAAATTTGTATGTATGTGTAAATATGTGCTTGCATATGTGAGAAAAGGTCTGGAAGGACACACAAGTAATGGTGGATACCTCTGCGGGTTAGGGCAGGTGAGTCGTGAGACAGGAAGGACTTTTCTTCTCCCTCAGATGCCTTTCTCTGCAGCTTCAGTCTTTCTCCTTATG... | ATGAGCAGAATGACGATAGTTCTAAGATAATACATATTAAATGGAAAAGAAGTTATTGAAAACTGTGTTGTGGAATAATCCATTTGTTTAAGACTGTTAAACACAAGCACATTGCATATGTATATAGACACATCTATACTTACATATGTAAATTTGTATGTATGTGTAAATATGTGCTTGCATATGTGAGAAAAGGTCTGGAAGGACACACAAGTAATGGTGGATACCTCTGCGGGTTAGGGCAGGTGAGTCGTGAGACAGGAAGGACTTTTCTTCTCCCTCAGATGCCTTTCTCTGCAGCTTCAGTCTTTCTCCTTATG... |
Task1_train_42764 | A mutation on Chromosome 13 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GAATGACGATAGTTCTAAGATAATACATATTAAATGGAAAAGAAGTTATTGAAAACTGTGTTGTGGAATAATCCATTTGTTTAAGACTGTTAAACACAAGCACATTGCATATGTATATAGACACATCTATACTTACATATGTAAATTTGTATGTATGTGTAAATATGTGCTTGCATATGTGAGAAAAGGTCTGGAAGGACACACAAGTAATGGTGGATACCTCTGCGGGTTAGGGCAGGTGAGTCGTGAGACAGGAAGGACTTTTCTTCTCCCTCAGATGCCTTTCTCTGCAGCTTCAGTCTTTCTCCTTATGATAATGT... | GAATGACGATAGTTCTAAGATAATACATATTAAATGGAAAAGAAGTTATTGAAAACTGTGTTGTGGAATAATCCATTTGTTTAAGACTGTTAAACACAAGCACATTGCATATGTATATAGACACATCTATACTTACATATGTAAATTTGTATGTATGTGTAAATATGTGCTTGCATATGTGAGAAAAGGTCTGGAAGGACACACAAGTAATGGTGGATACCTCTGCGGGTTAGGGCAGGTGAGTCGTGAGACAGGAAGGACTTTTCTTCTCCCTCAGATGCCTTTCTCTGCAGCTTCAGTCTTTCTCCTTATGATAATGT... |
Task1_train_42765 | A mutation on Chromosome 13 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GCTACTTTCTAATCAATGTGCCTTAAACCATACCAACAATACAAAAGTCCATCATTAGCGGTTCTTTCTTTCATTCCAGGCCAGTTCACACCTTTCCCCATTTCCACCTACATCGTTATCTGAAAATCCTTCCTTCTGACATAAAGTCAATGATCATATGAATAAGTGATCACTATTTTTTGTAAAATAGTTCAAAATATGCCAGTACTTAAATCTTTTAAGTCATTTATTTGCCTTGTGAATAATCCTGTGATTGACAAAATAGTGTTTTGAAGCATTCTTGTCTCATAAGGATAGTGGTGGCATTTGAAAGTTGAAGA... | GCTACTTTCTAATCAATGTGCCTTAAACCATACCAACAATACAAAAGTCCATCATTAGCGGTTCTTTCTTTCATTCCAGGCCAGTTCACACCTTTCCCCATTTCCACCTACATCGTTATCTGAAAATCCTTCCTTCTGACATAAAGTCAATGATCATATGAATAAGTGATCACTATTTTTTGTAAAATAGTTCAAAATATGCCAGTACTTAAATCTTTTAAGTCATTTATTTGCCTTGTGAATAATCCTGTGATTGACAAAATAGTGTTTTGAAGCATTCTTGTCTCATAAGGATAGTGGTGGCATTTGAAAGTTGAAGA... |
Task1_train_42766 | A genetic alteration is present on Chromosome 13. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | ATTATGTGACTGCTCTGACTCAAAATCTACCCTATTAGCTCAACTACAATGAGAAAAAACTCTACTGTAATTAATGGAGCACCTCAGGCTGACCTCATACTGTCCTTTCCTCTTTTTTTTCCTGTTCATTTTCTAGCATGTGCTATTCATAAATTTATCAAATAAGATTAGAAAATAAGCTGAAAGTCAGTGTCTAGGCTAGTAACCCTACAGAACTTATGCTATTCTATTACTACATTAAAAATATTTTAAAGAGATGAAGCAGTCATATTAATCCACCTTCAAGGTTAATGATCATAGTTTTTTCTAATTTGAACATA... | ATTATGTGACTGCTCTGACTCAAAATCTACCCTATTAGCTCAACTACAATGAGAAAAAACTCTACTGTAATTAATGGAGCACCTCAGGCTGACCTCATACTGTCCTTTCCTCTTTTTTTTCCTGTTCATTTTCTAGCATGTGCTATTCATAAATTTATCAAATAAGATTAGAAAATAAGCTGAAAGTCAGTGTCTAGGCTAGTAACCCTACAGAACTTATGCTATTCTATTACTACATTAAAAATATTTTAAAGAGATGAAGCAGTCATATTAATCCACCTTCAAGGTTAATGATCATAGTTTTTTCTAATTTGAACATA... |
Task1_train_42767 | Assess the clinical impact of this variant found on Chromosome 13. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | AATTAAGAGATGAGTCAAATTTTAATTTAAATTAAGAAATATAAAGGACAAAATTGCACAGCGAGAGCCACATTGAGAAGCCTTTCTAAACTGATTTAGACACATTTAAATGAAATGCTATTGTGGAAATTACTAAAGGTAAGTTAAGGATAATTACATCAAAGCTCTTTTTGGTCATTTGGTCCTGAAAACACCTGACACCACATTCAGGGACATTCTTGATTATACAGATTTCAGAGAAAATTGTACTGTAACCTAACTGACAAGTTTTGGTGTTTTTTCCAAAGAAGACAAAATCTCGAATCTGTTGCTAAAGTGAA... | AATTAAGAGATGAGTCAAATTTTAATTTAAATTAAGAAATATAAAGGACAAAATTGCACAGCGAGAGCCACATTGAGAAGCCTTTCTAAACTGATTTAGACACATTTAAATGAAATGCTATTGTGGAAATTACTAAAGGTAAGTTAAGGATAATTACATCAAAGCTCTTTTTGGTCATTTGGTCCTGAAAACACCTGACACCACATTCAGGGACATTCTTGATTATACAGATTTCAGAGAAAATTGTACTGTAACCTAACTGACAAGTTTTGGTGTTTTTTCCAAAGAAGACAAAATCTCGAATCTGTTGCTAAAGTGAA... |
Task1_train_42768 | A mutation located on Chromosome 13 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | AAATTTTTTCTTCATTGTTAAATCCCCATAGCACTACTCAATGTGAAGAAGATAGCAAATAAATTTTCCTGGGATGTTGAATCTTATGAAATTACTGACATTCAATTATTTTTGACCAACAAAATGGCAATTTTAAACAGTTCAATGTAATAGAATATAGTAATTTACATGGAAGGATACACACATGATAAAATGAACCTATAGATTAGTCCTAAAGATTAGTTAAAAGTCTTTCCAATTATTTTCTCTCCAGGATATATAACATATCATCCAATAATAAAGTGTAACAAATTAGGTTTCCTATTCAGGTCTTTTGGTGT... | AAATTTTTTCTTCATTGTTAAATCCCCATAGCACTACTCAATGTGAAGAAGATAGCAAATAAATTTTCCTGGGATGTTGAATCTTATGAAATTACTGACATTCAATTATTTTTGACCAACAAAATGGCAATTTTAAACAGTTCAATGTAATAGAATATAGTAATTTACATGGAAGGATACACACATGATAAAATGAACCTATAGATTAGTCCTAAAGATTAGTTAAAAGTCTTTCCAATTATTTTCTCTCCAGGATATATAACATATCATCCAATAATAAAGTGTAACAAATTAGGTTTCCTATTCAGGTCTTTTGGTGT... |
Task1_train_42769 | An alteration has been detected on Chromosome 13. Is it pathogenic, and if so, what disease is involved? | Benign | GTCAAGGAAAAAGAAGAACTCATTGAAGAGTGGCAACCAGAACCTCTTGTTCCTCCTGTCCCAAAAGACCATCCTGCTCTCAACTATAACATTGTTTTAGGACGGAGTCTTGCTCTGTCACCAGGCTGGAGTGCAGTGGTGCGATCTTGGCTCACTGCAACCTCCATCTCCCGGGTTCAAGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACAAGCCACCATGCCTGCCTAATTTTTGTATTTTCAGTAGAGATGGAGTTTCACCATGTTGGCCAGAATGATCTCGATCTCCTTTTTTTTAATTAA... | GTCAAGGAAAAAGAAGAACTCATTGAAGAGTGGCAACCAGAACCTCTTGTTCCTCCTGTCCCAAAAGACCATCCTGCTCTCAACTATAACATTGTTTTAGGACGGAGTCTTGCTCTGTCACCAGGCTGGAGTGCAGTGGTGCGATCTTGGCTCACTGCAACCTCCATCTCCCGGGTTCAAGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACAAGCCACCATGCCTGCCTAATTTTTGTATTTTCAGTAGAGATGGAGTTTCACCATGTTGGCCAGAATGATCTCGATCTCCTTTTTTTTAATTAA... |
Task1_train_42770 | This alteration occurs on Chromosome 13. Is it associated with a disease or is it a benign variant? | Benign | CTGCCTAATTTTTGTATTTTCAGTAGAGATGGAGTTTCACCATGTTGGCCAGAATGATCTCGATCTCCTTTTTTTTAATTAAAAAGTAAACTTTAATGTCAAAAATGCAAACTTGGGGAGGGCAGAAAGATCACACACAAGGCTGTCATTTCACACTTGGAAGGTTGCACAGCAGCCGGGCAGAGACGCTCCTCACTTCCCAGATGGTGAGGGGGCCAGGCAGAGGCGCTCCTCACTTCCCAGGTGGTGGGGGGGCTGGGCAGAGGCGCTCCTCCCTTACAAACGGTGAGGGGGCCGGGCAGAGGTGCTCCTCACTTTCC... | CTGCCTAATTTTTGTATTTTCAGTAGAGATGGAGTTTCACCATGTTGGCCAGAATGATCTCGATCTCCTTTTTTTTAATTAAAAAGTAAACTTTAATGTCAAAAATGCAAACTTGGGGAGGGCAGAAAGATCACACACAAGGCTGTCATTTCACACTTGGAAGGTTGCACAGCAGCCGGGCAGAGACGCTCCTCACTTCCCAGATGGTGAGGGGGCCAGGCAGAGGCGCTCCTCACTTCCCAGGTGGTGGGGGGGCTGGGCAGAGGCGCTCCTCCCTTACAAACGGTGAGGGGGCCGGGCAGAGGTGCTCCTCACTTTCC... |
Task1_train_42771 | Mutation context: Chromosome 13. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CTGGGCAGAGGCCCTCCTCACTTCGCAGACAGGATGGTGGCAAGGCAGAGGCGCTTCTCATTTCCCAGACGGTGAGGGGGCCGGGCAGAGGCACTCCTCACTTCGCAGACAGGATGGAGGCGAGGCAGAGGCGCTTCTCATTTCCCAGACGGTGAGGGGGCCGGGCAGAGGCACTTCTCACTTCGTAGACATGGCTGCGGCTGGGCAGAGGCCCTCCTCACTTCGCAGACAGGACGGCGGCGAGGCAGAGGCGCTCCTCATTTCCCAGACGGTGAGGGGGCCGGGCAGAGGCACTTCTCACTTCGTAGACATGGCTGCGG... | CTGGGCAGAGGCCCTCCTCACTTCGCAGACAGGATGGTGGCAAGGCAGAGGCGCTTCTCATTTCCCAGACGGTGAGGGGGCCGGGCAGAGGCACTCCTCACTTCGCAGACAGGATGGAGGCGAGGCAGAGGCGCTTCTCATTTCCCAGACGGTGAGGGGGCCGGGCAGAGGCACTTCTCACTTCGTAGACATGGCTGCGGCTGGGCAGAGGCCCTCCTCACTTCGCAGACAGGACGGCGGCGAGGCAGAGGCGCTCCTCATTTCCCAGACGGTGAGGGGGCCGGGCAGAGGCACTTCTCACTTCGTAGACATGGCTGCGG... |
Task1_train_42772 | This mutation occurs on Chromosome 13. Does this change lead to a known medical condition, or is it benign? | Benign | GCACTTCTCACTTCGTAGACATGGCTGCGGCTGGGCAGAGGCCCTCCTCACTTCGCAGACAGGACGGCGGCGAGGCAGAGGCGCTCCTCATTTCCCAGACAGTGAGGGGGCCGGGCAGAGGCACTTCTCACTTCGTAGACATGGCTGCGGCTGGGCAGAGGCACTCCTCACTTCGCAGACAGGACGGCGGCAAGGCAGAGACGCTCCTTACTTCCCAGATGGGGCAGCGGCTGGGCAGAGGTGCTCTTCACTTCCCATACCATGAGGTGGCCAGGCAGAGGTGTTCGTCACTTCCCAGATTGGGTGGAGGCCGGGCAGAG... | GCACTTCTCACTTCGTAGACATGGCTGCGGCTGGGCAGAGGCCCTCCTCACTTCGCAGACAGGACGGCGGCGAGGCAGAGGCGCTCCTCATTTCCCAGACAGTGAGGGGGCCGGGCAGAGGCACTTCTCACTTCGTAGACATGGCTGCGGCTGGGCAGAGGCACTCCTCACTTCGCAGACAGGACGGCGGCAAGGCAGAGACGCTCCTTACTTCCCAGATGGGGCAGCGGCTGGGCAGAGGTGCTCTTCACTTCCCATACCATGAGGTGGCCAGGCAGAGGTGTTCGTCACTTCCCAGATTGGGTGGAGGCCGGGCAGAG... |
Task1_train_42773 | This sequence variant lies on Chromosome 13. Is it clinically significant, and what condition might it cause if any? | Benign | CATCCAGGCTGGAGTGCAGTAGCGTGGTCACGGCTCACTGCAGCCTCATCCTCCTAGGCTCAAGTGATTCTCCCACCTCAGCCTCCTTAGTAACTGGGACTACAGTCACATGCCAGACTTGACCATTTTTTGTATTTTTTGGTAGAGATTGGGTTTCACCATATTGCCCAGGCTGGTCTTGAACACCTGAGCTCGAGCAGTCCGCTTCCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGCCAGCCACTGTGCCCAGTCCAACATGCTGTTCTTTCTAAATTCCAAAATTCATGTTCATTTTGCTACATCACATTCAAA... | CATCCAGGCTGGAGTGCAGTAGCGTGGTCACGGCTCACTGCAGCCTCATCCTCCTAGGCTCAAGTGATTCTCCCACCTCAGCCTCCTTAGTAACTGGGACTACAGTCACATGCCAGACTTGACCATTTTTTGTATTTTTTGGTAGAGATTGGGTTTCACCATATTGCCCAGGCTGGTCTTGAACACCTGAGCTCGAGCAGTCCGCTTCCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGCCAGCCACTGTGCCCAGTCCAACATGCTGTTCTTTCTAAATTCCAAAATTCATGTTCATTTTGCTACATCACATTCAAA... |
Task1_train_42774 | A variant was discovered on Chromosome 13. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | AAGTTCTTTTTTTCATGTCTTTTCTAACATAAGGAATTAGGTAAAATGGTGATGTTTCAGAGTCAAAAATTAAACAGACTGGAAAAAACACTGCCACGATCAGCTAAGTCAAGAAAATATTTTTGGCCTTAATTTTAAGAACTGATCTGTGAATACTGCATGTCTGAGACACAGGTGACATTCAATAAATGTTTATTGAGCTAAACTCATTTCACTAGTTTTGAATTATCCTCATGGAATTAATCCTTGATACTGTATATAAAGAAAAAGCTTAACTGTTAATTTTTAAGGAAAGTCTCCTGAATCAAAGATTTAAAAAA... | AAGTTCTTTTTTTCATGTCTTTTCTAACATAAGGAATTAGGTAAAATGGTGATGTTTCAGAGTCAAAAATTAAACAGACTGGAAAAAACACTGCCACGATCAGCTAAGTCAAGAAAATATTTTTGGCCTTAATTTTAAGAACTGATCTGTGAATACTGCATGTCTGAGACACAGGTGACATTCAATAAATGTTTATTGAGCTAAACTCATTTCACTAGTTTTGAATTATCCTCATGGAATTAATCCTTGATACTGTATATAAAGAAAAAGCTTAACTGTTAATTTTTAAGGAAAGTCTCCTGAATCAAAGATTTAAAAAA... |
Task1_train_42775 | Chromosome 13 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TAAACTTTGAGCATAAATGACATACTTTAGTTCACAGCAGCACTGACATTAAAATTGTCTACACAAAATGTGTAGAAAACCCAAAAAGTATGCTTATTTCTTCCACCTGAACTATTAATCATTTTAACTTTTTAATTTAGAATGCATGAGAGTGGCATTTGTTTAAGCTCAAATGTTCAAAGTTTTGAGCCACCCATGGCCTATATAATTGCAACCTTTCTATTTTTTCTTCACTATTACTATTTATAATTGTCAAGTTCCAGTTTCTTTTGCATTTATTGCAAGAAAGTTAGGTATGTTTGACAATACACATTTTTGAA... | TAAACTTTGAGCATAAATGACATACTTTAGTTCACAGCAGCACTGACATTAAAATTGTCTACACAAAATGTGTAGAAAACCCAAAAAGTATGCTTATTTCTTCCACCTGAACTATTAATCATTTTAACTTTTTAATTTAGAATGCATGAGAGTGGCATTTGTTTAAGCTCAAATGTTCAAAGTTTTGAGCCACCCATGGCCTATATAATTGCAACCTTTCTATTTTTTCTTCACTATTACTATTTATAATTGTCAAGTTCCAGTTTCTTTTGCATTTATTGCAAGAAAGTTAGGTATGTTTGACAATACACATTTTTGAA... |
Task1_train_42776 | A variant on Chromosome 13 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | AAGTCAAACTTAACTGAAAATTGCATTTTTTGAAAAATTTTATACTCTTCATCTAGCTTTGCCGGATATTAAAAAGTTGCCACATTTACCTTTTCTCTTTTTCTTTATACATCTGTATATTTATTGTTATTCTTGATTATTACTGAGCTGTTGTAGAGCAAGTTGTGGAAATTATACCCCTTTCATTTTAAATCCTCTAGCGTGTGTCTCCCAAGAGTACAGTATTCTCCTGTGTTACCACAGTATGATTTTATGTCCAGGAAATTTAACACTACATAATACTATTATCTAATAGAGAGCCAGCATACAAATTTTGCCCA... | AAGTCAAACTTAACTGAAAATTGCATTTTTTGAAAAATTTTATACTCTTCATCTAGCTTTGCCGGATATTAAAAAGTTGCCACATTTACCTTTTCTCTTTTTCTTTATACATCTGTATATTTATTGTTATTCTTGATTATTACTGAGCTGTTGTAGAGCAAGTTGTGGAAATTATACCCCTTTCATTTTAAATCCTCTAGCGTGTGTCTCCCAAGAGTACAGTATTCTCCTGTGTTACCACAGTATGATTTTATGTCCAGGAAATTTAACACTACATAATACTATTATCTAATAGAGAGCCAGCATACAAATTTTGCCCA... |
Task1_train_42777 | A genomic change on Chromosome 13 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CACAGCATTTAACATAAATCAGTCTGTTCCGATCACACCAACCTGACTGTTGCTTTCTCTAAAGTGGAATAACTTCTTCTTGACATAGGAACTTCTGTATACCCATGTGTGGAATACCCCCTTCTGTGTACCACCATGAGGAAGCCCAAATCAACTCATATAGAGTGACTATGATGGCGAGGATCAAGATTTCGGGAAGAAAAACAGTTAAGTTTTCAACGATGTATGAATCTCTCTCTCCAAGCAGGACTATAAACCCCTTTGTCAAGTGAGCAAATGAAAGTTCATGTTGGATTTAACATTGGTTGCAGATTGAACAT... | CACAGCATTTAACATAAATCAGTCTGTTCCGATCACACCAACCTGACTGTTGCTTTCTCTAAAGTGGAATAACTTCTTCTTGACATAGGAACTTCTGTATACCCATGTGTGGAATACCCCCTTCTGTGTACCACCATGAGGAAGCCCAAATCAACTCATATAGAGTGACTATGATGGCGAGGATCAAGATTTCGGGAAGAAAAACAGTTAAGTTTTCAACGATGTATGAATCTCTCTCTCCAAGCAGGACTATAAACCCCTTTGTCAAGTGAGCAAATGAAAGTTCATGTTGGATTTAACATTGGTTGCAGATTGAACAT... |
Task1_train_42778 | This variant is located on Chromosome 13. Evaluate its biological effect and specify any disease association. | Benign | TGAGCCTGCCACCCCAGGTCCCCACCTTTCTGTGACTCAGTGAGGCTTCCCAAGTCAGGCTCATTGCAAGGAAAACCTGGTTTAACTAGTAAAGAGGTGGGTTATAAAATATTGTTAGAAACACCGTGGTGGTTTAAATAATGTCTGCCAAAATGATGTGCTCGAGACCTAAGCCCTGGGACCTGTGAATGTCACTTTATTTGGAAATAAAGTCTTTGAAAATACAGTTAGGTTGGGTGCGGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCAAGGGGGCATGGATTGCTTGAGTCCAGGAGTTCAACGCCAGC... | TGAGCCTGCCACCCCAGGTCCCCACCTTTCTGTGACTCAGTGAGGCTTCCCAAGTCAGGCTCATTGCAAGGAAAACCTGGTTTAACTAGTAAAGAGGTGGGTTATAAAATATTGTTAGAAACACCGTGGTGGTTTAAATAATGTCTGCCAAAATGATGTGCTCGAGACCTAAGCCCTGGGACCTGTGAATGTCACTTTATTTGGAAATAAAGTCTTTGAAAATACAGTTAGGTTGGGTGCGGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCAAGGGGGCATGGATTGCTTGAGTCCAGGAGTTCAACGCCAGC... |
Task1_train_42779 | This variant is found on Chromosome 13. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CAATGATAGAGCTCCATCCACAGAAACACCTCTGGCGTCCTGGCTGTTAGAACCACTGGGAAAATGTTTGGGCTTCTTCTCTAATGCAGACAGAGGAGCTTGGCCTCCACCCTCACTTCGGCTCCCAAGTGGAGCTAAACCCTCAAAAGTACCTAAGGTCTCATGCCAGGGTAGTGAAGAAGATCTGAAGGGCCCCAATTCTGGCCAGTCACAAATTTCTTTGTACAAACCATTTGATATCTGCAAGTATCAGATAATACATGTGACAGGATCTTGAAAACCTGTAAAGTGTCATGCTTATTATGTATTGTTACAGTTAT... | CAATGATAGAGCTCCATCCACAGAAACACCTCTGGCGTCCTGGCTGTTAGAACCACTGGGAAAATGTTTGGGCTTCTTCTCTAATGCAGACAGAGGAGCTTGGCCTCCACCCTCACTTCGGCTCCCAAGTGGAGCTAAACCCTCAAAAGTACCTAAGGTCTCATGCCAGGGTAGTGAAGAAGATCTGAAGGGCCCCAATTCTGGCCAGTCACAAATTTCTTTGTACAAACCATTTGATATCTGCAAGTATCAGATAATACATGTGACAGGATCTTGAAAACCTGTAAAGTGTCATGCTTATTATGTATTGTTACAGTTAT... |
Task1_train_42780 | A mutation on Chromosome 13 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GTCTGTAATCCCAGCATTTTGGGAGGCTGAGGTGGGTGGATCACTTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACACGGTGAAACCTCGTCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGTGCACACCTGTAGTCCCAGCTACTCAAGAAGCTGAGGTGGGAAAATCGCTTGAACGCGGGAGAAGGAGGCTGCAGTGAGCCAAGACCGCACCCCTGCACGCCAGCCTGGGCGACAGAGTGAGACTCCATCTCAAAAAAAAAAAAAAAAAGAGAGAGAGAGAGAAAGAGAAAGAAAGAAAATCTTCTCTTA... | GTCTGTAATCCCAGCATTTTGGGAGGCTGAGGTGGGTGGATCACTTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACACGGTGAAACCTCGTCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGTGCACACCTGTAGTCCCAGCTACTCAAGAAGCTGAGGTGGGAAAATCGCTTGAACGCGGGAGAAGGAGGCTGCAGTGAGCCAAGACCGCACCCCTGCACGCCAGCCTGGGCGACAGAGTGAGACTCCATCTCAAAAAAAAAAAAAAAAAGAGAGAGAGAGAGAAAGAGAAAGAAAGAAAATCTTCTCTTA... |
Task1_train_42781 | This genomic variant is located on Chromosome 13. Can you determine its pathogenicity and name any linked disease? | Benign | TTAAGTACATCTTGACAGAACAACTGGTGAGTTCGAAAAATATTCACTCCAACAGTATTATATTTTTTCTCAAAAGCATTCTTATCCATCCCCTAAAGCAAAAGTTAAGACTGATGAAACTAATATGAGAACAGTAAATATATTAAATCATTTTGTTTAAAAAACTAATATTAGTATAAAATTTTAAATAATACTTTCAAAATCATTATTTGGTATAATTTTCTTTGAAAGAACATTTTTAAAAAAAGAATTCTGTTTTGACAAGTCATTTATAACATGCTTAAATCTTGTTACAAGTTGATACAGTTTGCTATTCATTC... | TTAAGTACATCTTGACAGAACAACTGGTGAGTTCGAAAAATATTCACTCCAACAGTATTATATTTTTTCTCAAAAGCATTCTTATCCATCCCCTAAAGCAAAAGTTAAGACTGATGAAACTAATATGAGAACAGTAAATATATTAAATCATTTTGTTTAAAAAACTAATATTAGTATAAAATTTTAAATAATACTTTCAAAATCATTATTTGGTATAATTTTCTTTGAAAGAACATTTTTAAAAAAAGAATTCTGTTTTGACAAGTCATTTATAACATGCTTAAATCTTGTTACAAGTTGATACAGTTTGCTATTCATTC... |
Task1_train_42782 | Here is a mutation located on Chromosome 13. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CCTGGGTCTGTGCCCTCAACCACGGCTCTGCTTTTGTCTGCAACCTGGCCATGGTGGTGGGTGGGTCGATGGGTGTGGTTCAAGGTCAAAATCACGTGGAAAGTTTTGCCGAAGTTCGCTCTGCCGCAGTTGCTTGCATAGCCGACTGCTAGGTAGCTTGGTTTGACTGACTTTTCACTAACTGACTTTTTATTGAGCTACCTGTTGGCCATTAAAAAACAGGAAGTATGTGAGACATGGTTTCAGTCTTCAAGGAATTCACAGCCAAAGTTGATATATGAGATAGGCTCTTATGAAAATTTACATAATCTGTGTCAGTT... | CCTGGGTCTGTGCCCTCAACCACGGCTCTGCTTTTGTCTGCAACCTGGCCATGGTGGTGGGTGGGTCGATGGGTGTGGTTCAAGGTCAAAATCACGTGGAAAGTTTTGCCGAAGTTCGCTCTGCCGCAGTTGCTTGCATAGCCGACTGCTAGGTAGCTTGGTTTGACTGACTTTTCACTAACTGACTTTTTATTGAGCTACCTGTTGGCCATTAAAAAACAGGAAGTATGTGAGACATGGTTTCAGTCTTCAAGGAATTCACAGCCAAAGTTGATATATGAGATAGGCTCTTATGAAAATTTACATAATCTGTGTCAGTT... |
Task1_train_42783 | Consider this mutation on Chromosome 13. Is this a benign change or a disease-causing variant? | Benign | GAGACCAGCCTGGGCAACATAGTGAGACCTCCATCTCTACAAAGAAAATTTAAAAGGTAGCCACGTGTGGTGCTGTGTGCCTATAGTCCCAGCTGCTTAGGAGGCTGAGATGGGAGGATTGCTTGAGCCAAGGAGGTTGATGCTGCAGAGCTGAGATTGTACCACTGCATTCCGGCCTGGGCAACAGAGCAAGACCCTGTCTCAAAGAAATCTGGACTTAATATAAAATTTTGAAAGATGTAAGGCTATGGAAAAACATAGTAAAAAATTATTCAAGAATATTTTGTAATGCATGAAAGCTTTTGAAAGGCTAATTTTAT... | GAGACCAGCCTGGGCAACATAGTGAGACCTCCATCTCTACAAAGAAAATTTAAAAGGTAGCCACGTGTGGTGCTGTGTGCCTATAGTCCCAGCTGCTTAGGAGGCTGAGATGGGAGGATTGCTTGAGCCAAGGAGGTTGATGCTGCAGAGCTGAGATTGTACCACTGCATTCCGGCCTGGGCAACAGAGCAAGACCCTGTCTCAAAGAAATCTGGACTTAATATAAAATTTTGAAAGATGTAAGGCTATGGAAAAACATAGTAAAAAATTATTCAAGAATATTTTGTAATGCATGAAAGCTTTTGAAAGGCTAATTTTAT... |
Task1_train_42784 | Here is a variant on Chromosome 13. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CCTACAGAACTGAATTCGGAAGTGCTGGAGCAGGTCAGTGATGGCGCTGTCCTATGATAACTCTGCTTTTCCCCACACTTCCTCCACGGAGCCCTGGGCTTCAGAGCGGGCTTTCTTGTTCTCTGTCCTTTCCTTTGGGGTTTTTAGCAGATGAGAATCTGATTATGGGCCTTGGCTTTGACCAGATATAGGCTTTGTGCCATGTGCCGGCAGCCTGGGCTCAGAGGCCGTGGAGTGTGTTGTGTTTTCAGCTGCCTTCTCATCTCCCATGCGGTGCTCTAAGCCACTGAGAACTCAGCTCAGCGGCGGAACCATCGCGG... | CCTACAGAACTGAATTCGGAAGTGCTGGAGCAGGTCAGTGATGGCGCTGTCCTATGATAACTCTGCTTTTCCCCACACTTCCTCCACGGAGCCCTGGGCTTCAGAGCGGGCTTTCTTGTTCTCTGTCCTTTCCTTTGGGGTTTTTAGCAGATGAGAATCTGATTATGGGCCTTGGCTTTGACCAGATATAGGCTTTGTGCCATGTGCCGGCAGCCTGGGCTCAGAGGCCGTGGAGTGTGTTGTGTTTTCAGCTGCCTTCTCATCTCCCATGCGGTGCTCTAAGCCACTGAGAACTCAGCTCAGCGGCGGAACCATCGCGG... |
Task1_train_42785 | Given a variant located on Chromosome 13, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CAGTCTCTAAAAACAAAACCATGCTGCCTCTTGCCTCCACACCTTGGTGCATTCCGTTCCTTCTGCTTAGAGTCCTGGCCACCACCTCCTTGGCCTTTCCTGGCCAGCTCTCTCTCGTCCTTTAAGCCTCAGCTTGTGCCTGGCACCTGATGTTGAGCTGACCTCCTGTCCGCCTTGTCCTGTCACACTGGCATTGCCTGTGTGTTGGCCGAGCCCGGAGGAAAGGACCCAGGGCCCCTCCTGGCTCTGAGGACTCCTCAGATCTGTCGCCCATGGGGGTGAGAGCGGTGTGTGGTTTTGAAGGCGCTGTTCTTGGCGGA... | CAGTCTCTAAAAACAAAACCATGCTGCCTCTTGCCTCCACACCTTGGTGCATTCCGTTCCTTCTGCTTAGAGTCCTGGCCACCACCTCCTTGGCCTTTCCTGGCCAGCTCTCTCTCGTCCTTTAAGCCTCAGCTTGTGCCTGGCACCTGATGTTGAGCTGACCTCCTGTCCGCCTTGTCCTGTCACACTGGCATTGCCTGTGTGTTGGCCGAGCCCGGAGGAAAGGACCCAGGGCCCCTCCTGGCTCTGAGGACTCCTCAGATCTGTCGCCCATGGGGGTGAGAGCGGTGTGTGGTTTTGAAGGCGCTGTTCTTGGCGGA... |
Task1_train_42786 | A mutation is present on Chromosome 13. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CGGGGAGCAGAAAGGAGGCATCGGAGGGACTTACATTTGAACCTTTTGAAGAGAGACCCTTGCAAAGCAAAATGTCCTCTTTCCATCCACCTGGGAGACAACTGGAAAAACACAACAGTGTCGTTAGTTCAGAATCATTGTGTTCGGAGGAGATAAAGCAATCCTCTGACCTCATATTCTGCTTTTTCTCCTTACGGGGTGATTCGCTTCTTTACCTTTTCCCCTACCATATCCCACAGAAGATTTGAGATTGCTTATTTTATTTTTTTTAAATGTACATAAATGAAAATGGAAAATTAAAAAAAAAATTAGGTAAATAG... | CGGGGAGCAGAAAGGAGGCATCGGAGGGACTTACATTTGAACCTTTTGAAGAGAGACCCTTGCAAAGCAAAATGTCCTCTTTCCATCCACCTGGGAGACAACTGGAAAAACACAACAGTGTCGTTAGTTCAGAATCATTGTGTTCGGAGGAGATAAAGCAATCCTCTGACCTCATATTCTGCTTTTTCTCCTTACGGGGTGATTCGCTTCTTTACCTTTTCCCCTACCATATCCCACAGAAGATTTGAGATTGCTTATTTTATTTTTTTTAAATGTACATAAATGAAAATGGAAAATTAAAAAAAAAATTAGGTAAATAG... |
Task1_train_42787 | This variant is found on Chromosome 13. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | AGAGCTCCTCTTTTCAGGCATTTGAAATACTTGGCATCTCTCCCAGAGAACAAATGGTTACATAAGGTCCTCCCAAAAGCACACATTAGCCACGGAGCCTAAGACTCAACTATCAAGAAATACAAATGACTAAATCACGGGATGAGTTGATGTCACACAAAAGAATCCAAACATTAATTCCAGCTGAGACAGAAAGGCTCTGAAAATGCTTCAGAGGAGAGGCGGCTCTCATTTTTCCTACAGCCATCCACTGAAACAACATGTTTGGAGCAAAACTGGCAGGAAGTCTAAGCCATGGCCACCGTGGTTTTGGCAGCCAT... | AGAGCTCCTCTTTTCAGGCATTTGAAATACTTGGCATCTCTCCCAGAGAACAAATGGTTACATAAGGTCCTCCCAAAAGCACACATTAGCCACGGAGCCTAAGACTCAACTATCAAGAAATACAAATGACTAAATCACGGGATGAGTTGATGTCACACAAAAGAATCCAAACATTAATTCCAGCTGAGACAGAAAGGCTCTGAAAATGCTTCAGAGGAGAGGCGGCTCTCATTTTTCCTACAGCCATCCACTGAAACAACATGTTTGGAGCAAAACTGGCAGGAAGTCTAAGCCATGGCCACCGTGGTTTTGGCAGCCAT... |
Task1_train_42788 | Here’s a variant located on Chromosome 13. What is the predicted biological effect — harmless or disease-causing? | Benign | AACAGTCGAAAGCAGGTGTGTTTTTAATTGAATCTTCAGCAACAACTCTTAGGGAAGCCTCCCAGGGCAGTAGCAACTGCTAATTTGAAGTAGAAAATAAATGTGCTGTTGTTTTTCTTTTGTGGGGTGGGGGAGGAGAAAAGAATGTTCTTCCCCAAATGATACACTGTTACCATACAGTCTGTAGATGTACTTAGGTACAGGAATGACTGGCAGAAGCCAACTTACCTACCTCTAAAACTGTAAAACTGTAACAGCTGAAAATCTGATCATCTTTTCCACTGAGAAACACTTAAGATCTTTCATACTGAGAAAACAAA... | AACAGTCGAAAGCAGGTGTGTTTTTAATTGAATCTTCAGCAACAACTCTTAGGGAAGCCTCCCAGGGCAGTAGCAACTGCTAATTTGAAGTAGAAAATAAATGTGCTGTTGTTTTTCTTTTGTGGGGTGGGGGAGGAGAAAAGAATGTTCTTCCCCAAATGATACACTGTTACCATACAGTCTGTAGATGTACTTAGGTACAGGAATGACTGGCAGAAGCCAACTTACCTACCTCTAAAACTGTAAAACTGTAACAGCTGAAAATCTGATCATCTTTTCCACTGAGAAACACTTAAGATCTTTCATACTGAGAAAACAAA... |
Task1_train_42789 | This mutation is located on Chromosome 13. Is it associated with a disease or is it a benign polymorphism? | Benign | GGCCAGGCCGATCAAGGACAGCACCCTGGGAAAGACAGGGTGTTAGGGCCAACATGGCAGATCCTCGCAAGTAGAAGGCCTCTCTTTTCCCCAGTTTCCCTCAGTGGGCCTGGCATAGTGACACACATAGAGAAGAAGACAATCTCGCGAGAAGCCAGCTCACAGGAATGCAGCGTGATAGTCAAATGCAAACTTGAACTCATGGGCCTTCAAACTCCTGCCCCCATCTAATAATTTACCATCCGGAAAACATAAAACAGTAGCTTGCGAGCTGAGCAAAGCCTTAGGTTTGGGGTTCTTTTGTAGCTTTATTGTTTCCA... | GGCCAGGCCGATCAAGGACAGCACCCTGGGAAAGACAGGGTGTTAGGGCCAACATGGCAGATCCTCGCAAGTAGAAGGCCTCTCTTTTCCCCAGTTTCCCTCAGTGGGCCTGGCATAGTGACACACATAGAGAAGAAGACAATCTCGCGAGAAGCCAGCTCACAGGAATGCAGCGTGATAGTCAAATGCAAACTTGAACTCATGGGCCTTCAAACTCCTGCCCCCATCTAATAATTTACCATCCGGAAAACATAAAACAGTAGCTTGCGAGCTGAGCAAAGCCTTAGGTTTGGGGTTCTTTTGTAGCTTTATTGTTTCCA... |
Task1_train_42790 | This sequence variant lies on Chromosome 13. Is it clinically significant, and what condition might it cause if any? | Benign | AGTATCTGTAAGCCCTCCCAGATTCTTCCTTCTGCAATTCAGAACCATCACAATGCATTTCCTATTTCCCATTCAGCCAGGGGCCCTCACATGCCAGAGCAGGCCCACCTGCTTCCCTGCATTTTGTATCTGTTCCATCACAGGTTTCATCAGACAAGTGACCACAGACAGACGAGACTAAGAGTTAAGACAACAGCCGGGCATCTGGCTCTTCATGCTTAAGGGTGTCCAGGGAAAACGGATGTACTACTAAAGTATCATGAGATAACACAGTTGGCAGCCTGTCACACGTGGGAATGGACACTCCTAGGTCACCATTA... | AGTATCTGTAAGCCCTCCCAGATTCTTCCTTCTGCAATTCAGAACCATCACAATGCATTTCCTATTTCCCATTCAGCCAGGGGCCCTCACATGCCAGAGCAGGCCCACCTGCTTCCCTGCATTTTGTATCTGTTCCATCACAGGTTTCATCAGACAAGTGACCACAGACAGACGAGACTAAGAGTTAAGACAACAGCCGGGCATCTGGCTCTTCATGCTTAAGGGTGTCCAGGGAAAACGGATGTACTACTAAAGTATCATGAGATAACACAGTTGGCAGCCTGTCACACGTGGGAATGGACACTCCTAGGTCACCATTA... |
Task1_train_42791 | Assess the clinical impact of this variant found on Chromosome 13. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | ATTTGCCTTGACTTTCATATATAAATGTCGAAGTTGCTTTATGAACACATCTTGGATGACTTGTTGCATTTTTATTTTCCCCTCCGGAGTTGCAGGTTTTTGTGCTGTCTTTAATCCTGAGACCATGTGCTTGATCCTAATGCAAATAATTCAATTAGTTTGATTTTAAAATTCCTTCCTTCTCCCCTGTGGTTTTACGAGAGTCTCTTAAAGCAAAAACGAATTCTGGAAAGATATAAATAACTTATAGTGCAAGCAAAATGAGTTAACTCAAAGTTTCTCCAAAAATGAGATGAACTACAATTTGAACATTATAACTA... | ATTTGCCTTGACTTTCATATATAAATGTCGAAGTTGCTTTATGAACACATCTTGGATGACTTGTTGCATTTTTATTTTCCCCTCCGGAGTTGCAGGTTTTTGTGCTGTCTTTAATCCTGAGACCATGTGCTTGATCCTAATGCAAATAATTCAATTAGTTTGATTTTAAAATTCCTTCCTTCTCCCCTGTGGTTTTACGAGAGTCTCTTAAAGCAAAAACGAATTCTGGAAAGATATAAATAACTTATAGTGCAAGCAAAATGAGTTAACTCAAAGTTTCTCCAAAAATGAGATGAACTACAATTTGAACATTATAACTA... |
Task1_train_42792 | This is a variant located on Chromosome 13. Is this mutation a likely cause of disease or not? | Benign | TCCATGCTGTCCCACTCGGAAGTAGGGCTGGGCCGGGCCAGGCCAGGCCAGCCCAGCCCAGCTCTTAGCTTCCCCATCGTTGGATCCTCGGACCACCTCTGGACAGAGGAAAAACACCCAGAGTGAAGAAAAGGAAACAGGTGGTTCAACTTCCTCTGCTTAGGGTCCAGGAAGGAGCAAACGTGGGCCCATCAGTGCATGTAGCAAGAACAGGAACCCCACCGGGTTTCAGTCCAGCTTCGTCTAATAGAGACTGTCTTTATGTGCTTTGTCATAAGAAAAGTCAAGCAGCTAATAAATAGCAGAACCGACCGGGCGCA... | TCCATGCTGTCCCACTCGGAAGTAGGGCTGGGCCGGGCCAGGCCAGGCCAGCCCAGCCCAGCTCTTAGCTTCCCCATCGTTGGATCCTCGGACCACCTCTGGACAGAGGAAAAACACCCAGAGTGAAGAAAAGGAAACAGGTGGTTCAACTTCCTCTGCTTAGGGTCCAGGAAGGAGCAAACGTGGGCCCATCAGTGCATGTAGCAAGAACAGGAACCCCACCGGGTTTCAGTCCAGCTTCGTCTAATAGAGACTGTCTTTATGTGCTTTGTCATAAGAAAAGTCAAGCAGCTAATAAATAGCAGAACCGACCGGGCGCA... |
Task1_train_42793 | Chromosome 13 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CCATATATGTATATATATATATTTTTTAATGAAGCCACAAGCATTCTGCCTCTGTGCTTTTTATTTATTTATTTATTTATTTTTGAGACGGAGGTTCGCTCTGGTTGCCCAGGCAGGAGTGCAATGGCACAATCTCGGCTCACCGCAACCTCTGCCCCCCAGGTTCAAGTGATTCTCATGTCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATGCGCCACCATGCACGGCTAATTTTGCATTTTTAGTAGAGACAGGGTTTCTCCATGTTGGTTGGGCTGGTCTTGAAGTCCCGACCTCAGGTGATCCACCCGCCTCGG... | CCATATATGTATATATATATATTTTTTAATGAAGCCACAAGCATTCTGCCTCTGTGCTTTTTATTTATTTATTTATTTATTTTTGAGACGGAGGTTCGCTCTGGTTGCCCAGGCAGGAGTGCAATGGCACAATCTCGGCTCACCGCAACCTCTGCCCCCCAGGTTCAAGTGATTCTCATGTCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATGCGCCACCATGCACGGCTAATTTTGCATTTTTAGTAGAGACAGGGTTTCTCCATGTTGGTTGGGCTGGTCTTGAAGTCCCGACCTCAGGTGATCCACCCGCCTCGG... |
Task1_train_42794 | This alteration on Chromosome 13 may affect genome function. Does it lead to a disease or is it benign? | Benign | CTGCAGTAGGGGTAACGTTTATTAATGAGAAATGTCTCAGAGAGAGGAAGAACTAGGGTTTTATAAATGCAGGTGAACAAGGGAGGGGTCCAAGAATTACGGGGTTCATGAAGAAGAGTGGAAGTCTATGGGGAAGGTTGCTTTGCCTCCAGCCATTTCCTGGGTTAAGAAAGAGGAGGAAGATTCTGTAACTGTTTCTGTGTTCTAGGAGCACGGGGCTCAGGGAAAGTTCAGCATTGTCAGTTGTCAACAAAATCAGTAAGTGTTATTAAATACCCCATGGTGTGTGGTTCTGGCACTGAAATGGGGCTGTTTCCTAA... | CTGCAGTAGGGGTAACGTTTATTAATGAGAAATGTCTCAGAGAGAGGAAGAACTAGGGTTTTATAAATGCAGGTGAACAAGGGAGGGGTCCAAGAATTACGGGGTTCATGAAGAAGAGTGGAAGTCTATGGGGAAGGTTGCTTTGCCTCCAGCCATTTCCTGGGTTAAGAAAGAGGAGGAAGATTCTGTAACTGTTTCTGTGTTCTAGGAGCACGGGGCTCAGGGAAAGTTCAGCATTGTCAGTTGTCAACAAAATCAGTAAGTGTTATTAAATACCCCATGGTGTGTGGTTCTGGCACTGAAATGGGGCTGTTTCCTAA... |
Task1_train_42795 | Given this variant on Chromosome 13, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CGCGGAGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGATGGGCGAATCACGAGGTCAGGAGTTCGAGACCAGCCTGGCTAACATAGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCGGGCATAGTGGCGCATGCCTGTCCTAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCGAGATCAGGCCACTGCACTCCAGCCTGGGCAACAGAGCAAGACTCCATCTCAGGGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGCTAACACTTTCTGA... | CGCGGAGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGATGGGCGAATCACGAGGTCAGGAGTTCGAGACCAGCCTGGCTAACATAGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCGGGCATAGTGGCGCATGCCTGTCCTAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCGAGATCAGGCCACTGCACTCCAGCCTGGGCAACAGAGCAAGACTCCATCTCAGGGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGCTAACACTTTCTGA... |
Task1_train_42796 | Here is a variant on Chromosome 13. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CTGTAATCGTTGCACTTTGGGAGGCATAGGCAGGAGAATCCCTTGAGCCCAGGGGTTCGAGGTTGCAGTGAACTATGATCATGCCACTGCATTCTAGCCTGGGCAACAGAGCAAGACCTTGAGAGACCTTTGCTCTTTCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTAAGAGTACAGCAAAGAGAATATATATATATATATATATATATATATATATATTTAGAGAGGGAGAGAGAGAGAAAGAGAGACCTTGAGAGACCTTCTTGCTCTTATGTTGTAGATACCAAATCACTGATGACAAGCATTG... | CTGTAATCGTTGCACTTTGGGAGGCATAGGCAGGAGAATCCCTTGAGCCCAGGGGTTCGAGGTTGCAGTGAACTATGATCATGCCACTGCATTCTAGCCTGGGCAACAGAGCAAGACCTTGAGAGACCTTTGCTCTTTCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTAAGAGTACAGCAAAGAGAATATATATATATATATATATATATATATATATATTTAGAGAGGGAGAGAGAGAGAAAGAGAGACCTTGAGAGACCTTCTTGCTCTTATGTTGTAGATACCAAATCACTGATGACAAGCATTG... |
Task1_train_42797 | Chromosome 13 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TCATGAAACTGAGCCTCCATGAACCCACTTCAGGGGATAAGCAACTTAGAATATTGCTTCTATTGATGCGTCATTGGGTCAATTTGGAAGGGATGGATCTCTCCCTATCCTGTATACATTTTGTTTATTTTCCCCCTTTCTTTCTATTTTTAACCATCTCACCTTTAAAAAGATGTTCCTTTGACCCACAAATTATTTCCCATCTCTACTGTGTATACTTTAGGATCTAAGATGTCCTATTTAATATAAAATTTAAAAAATCACATTGAGTAGTCTTTTATTCCTGATTCACCAAATTACTGCTACCATAATGCTTTATC... | TCATGAAACTGAGCCTCCATGAACCCACTTCAGGGGATAAGCAACTTAGAATATTGCTTCTATTGATGCGTCATTGGGTCAATTTGGAAGGGATGGATCTCTCCCTATCCTGTATACATTTTGTTTATTTTCCCCCTTTCTTTCTATTTTTAACCATCTCACCTTTAAAAAGATGTTCCTTTGACCCACAAATTATTTCCCATCTCTACTGTGTATACTTTAGGATCTAAGATGTCCTATTTAATATAAAATTTAAAAAATCACATTGAGTAGTCTTTTATTCCTGATTCACCAAATTACTGCTACCATAATGCTTTATC... |
Task1_train_42798 | A mutation found on Chromosome 13 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | ATTTACTAGTCTTTCTTTTTTGATGGGAATTGCATGACATAAGGTTCACCAGAATTTTTGTGTTTGCGCAGTATAAACCCATACCAATACCACAAACAGCAAGGACATCTGTATGTGAAGTCACACATTTTATGCATCCCAACCTATTGGTTTGCACCTTACCATATCTGATGTATCCCTTTCTGATGAAGTCTGGTGGTTCCTGATGAAATGGTATGCAAAATTGCCAGAATCAGTAAAAGTGCCTGAACTTTCTAAATTGCTAATGATAAATAACAAATTTCAATCTATCATTGGAAGATTGGATTACTTTCTATCTT... | ATTTACTAGTCTTTCTTTTTTGATGGGAATTGCATGACATAAGGTTCACCAGAATTTTTGTGTTTGCGCAGTATAAACCCATACCAATACCACAAACAGCAAGGACATCTGTATGTGAAGTCACACATTTTATGCATCCCAACCTATTGGTTTGCACCTTACCATATCTGATGTATCCCTTTCTGATGAAGTCTGGTGGTTCCTGATGAAATGGTATGCAAAATTGCCAGAATCAGTAAAAGTGCCTGAACTTTCTAAATTGCTAATGATAAATAACAAATTTCAATCTATCATTGGAAGATTGGATTACTTTCTATCTT... |
Task1_train_42799 | A genomic change on Chromosome 13 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | AGCTGAACCAGTAGCATTTCTCTGGGTCCTTAAATCAACAGATTCACATGTATTTCTTTCTTGAAACCATACATGATATTGTTTGTTTTTTTCTGGAGTCACATGGAATTCTGACTCTGAAAGAACTTGAGTATCTTTCTTCCTCGGGCTGTGCAGATCACGGTCAGAAGCACACACAAGGGTTGGCTGTGGGAATTTTCTGATGAGTGATGAGTTTTCATGGGGACTTTGCTTTTTGAAAGAAATATGTTGTTCTAACAGTTCTGTATCAATGGAAAGACTACCACTTTGTCCACCAGCATTTACGTTTTTACACACTG... | AGCTGAACCAGTAGCATTTCTCTGGGTCCTTAAATCAACAGATTCACATGTATTTCTTTCTTGAAACCATACATGATATTGTTTGTTTTTTTCTGGAGTCACATGGAATTCTGACTCTGAAAGAACTTGAGTATCTTTCTTCCTCGGGCTGTGCAGATCACGGTCAGAAGCACACACAAGGGTTGGCTGTGGGAATTTTCTGATGAGTGATGAGTTTTCATGGGGACTTTGCTTTTTGAAAGAAATATGTTGTTCTAACAGTTCTGTATCAATGGAAAGACTACCACTTTGTCCACCAGCATTTACGTTTTTACACACTG... |
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