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_46700 | Consider this mutation on Chromosome 19. Is this a benign change or a disease-causing variant? | Benign | CCATGCCTCTAATCCCAGTTACTGGGGAGGCTGAAACAGGAGGCTGGCTTGTGCAAAGGAGTTCGAGACCAGCCTGGGCAACATAGCAAGACCCCGCCCCTACAAAAGATAGAAAAAATTAGCCAGGCGTGGTGGTGCATGCCTGTAGCCCCAGCTACTCTGGAGGCTGAGGTGGGAGGATCGTTTAAGCCCAGGAGGTGTTCGCTACAGTGAGCTATGATCACGCCACTGCACTCCAGCCCAGGCAACAGAGCAACATCCCAACTCTAAAAATAATATAAAATAAGATGGGCAAATTGGAGCCAGAGAGGTGAGACCTG... | CCATGCCTCTAATCCCAGTTACTGGGGAGGCTGAAACAGGAGGCTGGCTTGTGCAAAGGAGTTCGAGACCAGCCTGGGCAACATAGCAAGACCCCGCCCCTACAAAAGATAGAAAAAATTAGCCAGGCGTGGTGGTGCATGCCTGTAGCCCCAGCTACTCTGGAGGCTGAGGTGGGAGGATCGTTTAAGCCCAGGAGGTGTTCGCTACAGTGAGCTATGATCACGCCACTGCACTCCAGCCCAGGCAACAGAGCAACATCCCAACTCTAAAAATAATATAAAATAAGATGGGCAAATTGGAGCCAGAGAGGTGAGACCTG... |
Task1_train_46701 | Here’s a variant located on Chromosome 19. What is the predicted biological effect — harmless or disease-causing? | Benign | AACACTGGCATGGAGAAGAGAAAGGAGGTTCCAAAGCAGAACAAGAGGGTCAGAACTCAGTGTTAGGACAGCCAGCCAGCATCACTCATGGACGGCAAAAGGGAACTGGGTGCAGACAGATGCAGGGCCAGGGATGTGGCCCACTTTCCCCTTGCATGACACTGGGCTCTGTTGGCCTTGCCCCACTCCTGCTGCTGCAATTGGGGTGAAGATGCCCCAGGTTTGTTTTTGTTTTTTGTTTTTTGTTTTTTTATTTGAGACGAAGTCTCACTCTGTCTCCCAGGCTGGAGTGCAGTGGTGTGATCTTGGCTCACTGCAAC... | AACACTGGCATGGAGAAGAGAAAGGAGGTTCCAAAGCAGAACAAGAGGGTCAGAACTCAGTGTTAGGACAGCCAGCCAGCATCACTCATGGACGGCAAAAGGGAACTGGGTGCAGACAGATGCAGGGCCAGGGATGTGGCCCACTTTCCCCTTGCATGACACTGGGCTCTGTTGGCCTTGCCCCACTCCTGCTGCTGCAATTGGGGTGAAGATGCCCCAGGTTTGTTTTTGTTTTTTGTTTTTTGTTTTTTTATTTGAGACGAAGTCTCACTCTGTCTCCCAGGCTGGAGTGCAGTGGTGTGATCTTGGCTCACTGCAAC... |
Task1_train_46702 | A mutation on Chromosome 19 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CAAAGCAGAACAAGAGGGTCAGAACTCAGTGTTAGGACAGCCAGCCAGCATCACTCATGGACGGCAAAAGGGAACTGGGTGCAGACAGATGCAGGGCCAGGGATGTGGCCCACTTTCCCCTTGCATGACACTGGGCTCTGTTGGCCTTGCCCCACTCCTGCTGCTGCAATTGGGGTGAAGATGCCCCAGGTTTGTTTTTGTTTTTTGTTTTTTGTTTTTTTATTTGAGACGAAGTCTCACTCTGTCTCCCAGGCTGGAGTGCAGTGGTGTGATCTTGGCTCACTGCAACCTCCGCCTCCAGGTTCAAGCAATTATCGTGC... | CAAAGCAGAACAAGAGGGTCAGAACTCAGTGTTAGGACAGCCAGCCAGCATCACTCATGGACGGCAAAAGGGAACTGGGTGCAGACAGATGCAGGGCCAGGGATGTGGCCCACTTTCCCCTTGCATGACACTGGGCTCTGTTGGCCTTGCCCCACTCCTGCTGCTGCAATTGGGGTGAAGATGCCCCAGGTTTGTTTTTGTTTTTTGTTTTTTGTTTTTTTATTTGAGACGAAGTCTCACTCTGTCTCCCAGGCTGGAGTGCAGTGGTGTGATCTTGGCTCACTGCAACCTCCGCCTCCAGGTTCAAGCAATTATCGTGC... |
Task1_train_46703 | Given this context: Chromosome 19 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AGACAGATGCAGGGCCAGGGATGTGGCCCACTTTCCCCTTGCATGACACTGGGCTCTGTTGGCCTTGCCCCACTCCTGCTGCTGCAATTGGGGTGAAGATGCCCCAGGTTTGTTTTTGTTTTTTGTTTTTTGTTTTTTTATTTGAGACGAAGTCTCACTCTGTCTCCCAGGCTGGAGTGCAGTGGTGTGATCTTGGCTCACTGCAACCTCCGCCTCCAGGTTCAAGCAATTATCGTGCCTCAGCCTCCTGAGTCACTGGCATTACAGGTGTCCACCATCATGTCTGGCTAATTTTTGTATTTTCAGTAGAGACAGTATTT... | AGACAGATGCAGGGCCAGGGATGTGGCCCACTTTCCCCTTGCATGACACTGGGCTCTGTTGGCCTTGCCCCACTCCTGCTGCTGCAATTGGGGTGAAGATGCCCCAGGTTTGTTTTTGTTTTTTGTTTTTTGTTTTTTTATTTGAGACGAAGTCTCACTCTGTCTCCCAGGCTGGAGTGCAGTGGTGTGATCTTGGCTCACTGCAACCTCCGCCTCCAGGTTCAAGCAATTATCGTGCCTCAGCCTCCTGAGTCACTGGCATTACAGGTGTCCACCATCATGTCTGGCTAATTTTTGTATTTTCAGTAGAGACAGTATTT... |
Task1_train_46704 | A mutation has occurred on Chromosome 19. What is the medical relevance of this mutation? | Benign | GACAGAGAGAGACTCCATCTCAATAAATAAATTAATTAAATTAAATTAAATTAAAGATATCTCAGACATAAGAGAGGGGAGCCCATTGGAGCAGATGTGTCTCAGGTGGGAAAGGGACTGAGAAGGAGCTTTGGGTGGGAGGTGGGGAGGAGCCGGTGCTGAAAGGCTTAATGTCCGGGCACCTACAAAGGGATGGGAATCTCCAGGAAGGTGGGTGTCTGTTGTACTGTAGCCCACTCACAATGTAACATTATGCTGAAAGACCAAAAAAGGTTACAAAACTTTAAACAGGTGGGAATATAAAATAGTGCAGCCACATT... | GACAGAGAGAGACTCCATCTCAATAAATAAATTAATTAAATTAAATTAAATTAAAGATATCTCAGACATAAGAGAGGGGAGCCCATTGGAGCAGATGTGTCTCAGGTGGGAAAGGGACTGAGAAGGAGCTTTGGGTGGGAGGTGGGGAGGAGCCGGTGCTGAAAGGCTTAATGTCCGGGCACCTACAAAGGGATGGGAATCTCCAGGAAGGTGGGTGTCTGTTGTACTGTAGCCCACTCACAATGTAACATTATGCTGAAAGACCAAAAAAGGTTACAAAACTTTAAACAGGTGGGAATATAAAATAGTGCAGCCACATT... |
Task1_train_46705 | A change on Chromosome 19 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GGGCGCTGGAGAGGACGCAGGCTGCCGTGTACCTCCAGGCCTCATGGAGGGGCTACTGGCAGCGGAAGCTCTACCGGCACCAGAAACAGAGCATCATCCGCCTGCAGAGCCTGTGTCGGGGGCACCTGCAGCGCAAGAGGTGAGCAGAGCCGGGCCACGCTCCTCGGAATATTCCAGAAGCCAAAAAGGTCACTCACCAAATTGCTGCCCGTGATATACCATCTGGCCTGTGGCACTAAGGGGATGTCATTCTGGACACAGGGAAAGGCTGGTGGGAAACCAGATGCCTAGGCACTCATGGGCTGCAGAGAAGTGCTCCA... | GGGCGCTGGAGAGGACGCAGGCTGCCGTGTACCTCCAGGCCTCATGGAGGGGCTACTGGCAGCGGAAGCTCTACCGGCACCAGAAACAGAGCATCATCCGCCTGCAGAGCCTGTGTCGGGGGCACCTGCAGCGCAAGAGGTGAGCAGAGCCGGGCCACGCTCCTCGGAATATTCCAGAAGCCAAAAAGGTCACTCACCAAATTGCTGCCCGTGATATACCATCTGGCCTGTGGCACTAAGGGGATGTCATTCTGGACACAGGGAAAGGCTGGTGGGAAACCAGATGCCTAGGCACTCATGGGCTGCAGAGAAGTGCTCCA... |
Task1_train_46706 | This variant is found on Chromosome 19. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CAGGGCCCAGGAATGACCCAGCTGATCCATGCTCACACAGCTTTGATATGGCCAAGTCAGTACCCAAGCCCAGGCAGCCTCCAGAGGCCCAGCAGGGTCAAGAGGGCCTCTCCTACATGTGTTTTTCTGCCAGAACCATTTGGGCCAGGGTCTTTTCAGCCCAGAAGGCAGCCCCACCACCCCACATCTGTCCAACAGTCAGTTGTCATGGTCCTGAGATAAGGATGCGGGACCCAGGCCCGTCCCCTCACCTGATTCCATCCTTGCCAGGTGCCAGACACTCTCTTCTTTAGCGTAACCAGTGTACCCTCTGCAAGGCG... | CAGGGCCCAGGAATGACCCAGCTGATCCATGCTCACACAGCTTTGATATGGCCAAGTCAGTACCCAAGCCCAGGCAGCCTCCAGAGGCCCAGCAGGGTCAAGAGGGCCTCTCCTACATGTGTTTTTCTGCCAGAACCATTTGGGCCAGGGTCTTTTCAGCCCAGAAGGCAGCCCCACCACCCCACATCTGTCCAACAGTCAGTTGTCATGGTCCTGAGATAAGGATGCGGGACCCAGGCCCGTCCCCTCACCTGATTCCATCCTTGCCAGGTGCCAGACACTCTCTTCTTTAGCGTAACCAGTGTACCCTCTGCAAGGCG... |
Task1_train_46707 | The following genetic variant occurs on Chromosome 19. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | ACCATCCTGGCTAACACGGTGAAACCTCGTCTCTACTAAAAAATAGAAAAAATTAGCCGGGCGTGGTGGTGGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGTTTGAACCCTGGAGGCGGAGCTTGCAGTGAGCCGAGATCGCGCCACTGTACTCCAGCCTAGGAGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAAAGAAAAGAAAGTACAGGTGAGGGAATCCGTTATCATGCCAGTGCCGCCAAGGTTGTGGGAAAACCCCTGTATCTCTTGGAGCATAAATGGTACAATCTCACTAA... | ACCATCCTGGCTAACACGGTGAAACCTCGTCTCTACTAAAAAATAGAAAAAATTAGCCGGGCGTGGTGGTGGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGTTTGAACCCTGGAGGCGGAGCTTGCAGTGAGCCGAGATCGCGCCACTGTACTCCAGCCTAGGAGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAAAGAAAAGAAAGTACAGGTGAGGGAATCCGTTATCATGCCAGTGCCGCCAAGGTTGTGGGAAAACCCCTGTATCTCTTGGAGCATAAATGGTACAATCTCACTAA... |
Task1_train_46708 | This variant is present on Chromosome 19. Is the change likely to result in a pathogenic outcome? | Benign | AACTTGGCAGTATGTTCCAAATGTAAAATACACACATCCCAGACAGGAGGCTGAGGCAGGAGGATCGCTTGAGTCCAGGAGTTGGAAAACAGCCTGGACCCATAAGGACATTTCCTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATGCCAAGCACGATTATGGGATCACACCTGTAATCCCAGCACTGTGGGAGGCTGAGGCGGGTGGATTGCTGGAACTCGGGAGTTCAAGACCAGCCTGAGCAACGCGGCGAGATCCCGTCTCTACAAAAAACACAAAAATTAGGGAGGCGTTGTGTCACCTGTGGTTCCAGCT... | AACTTGGCAGTATGTTCCAAATGTAAAATACACACATCCCAGACAGGAGGCTGAGGCAGGAGGATCGCTTGAGTCCAGGAGTTGGAAAACAGCCTGGACCCATAAGGACATTTCCTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATGCCAAGCACGATTATGGGATCACACCTGTAATCCCAGCACTGTGGGAGGCTGAGGCGGGTGGATTGCTGGAACTCGGGAGTTCAAGACCAGCCTGAGCAACGCGGCGAGATCCCGTCTCTACAAAAAACACAAAAATTAGGGAGGCGTTGTGTCACCTGTGGTTCCAGCT... |
Task1_train_46709 | Here’s a variant located on Chromosome 19. What is the predicted biological effect — harmless or disease-causing? | Benign | GAGGCTGAGGCAGGAGGATCGCTTGAGTCCAGGAGTTGGAAAACAGCCTGGACCCATAAGGACATTTCCTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATGCCAAGCACGATTATGGGATCACACCTGTAATCCCAGCACTGTGGGAGGCTGAGGCGGGTGGATTGCTGGAACTCGGGAGTTCAAGACCAGCCTGAGCAACGCGGCGAGATCCCGTCTCTACAAAAAACACAAAAATTAGGGAGGCGTTGTGTCACCTGTGGTTCCAGCTATTTGGGAGGCTGAGGTGGAAGGATCAATTGAGGCTAGGAAGGAGG... | GAGGCTGAGGCAGGAGGATCGCTTGAGTCCAGGAGTTGGAAAACAGCCTGGACCCATAAGGACATTTCCTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATGCCAAGCACGATTATGGGATCACACCTGTAATCCCAGCACTGTGGGAGGCTGAGGCGGGTGGATTGCTGGAACTCGGGAGTTCAAGACCAGCCTGAGCAACGCGGCGAGATCCCGTCTCTACAAAAAACACAAAAATTAGGGAGGCGTTGTGTCACCTGTGGTTCCAGCTATTTGGGAGGCTGAGGTGGAAGGATCAATTGAGGCTAGGAAGGAGG... |
Task1_train_46710 | Chromosome 19 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CAGGAACTCAGGTCTTAGACTCTGGGGCTCGGCAGGGTACAGGGAAGAAATTCAGCTTCTCTGCCCCACCCCAACACGAGCAAGGTGGTCTGCCTCCATTTCCCTGCTTTCTTCAAAGTTGGCCCAAGTCCAGGGACAGCGTGTGGGTCGGAAGGTGACTAGCCCCAGCCCTCGCTGGAGGGGACTGTGCTCGCCACCATACTTCTTGTTCTGTTTCTGGGGTCAGGTTGACTGGATTCAAGTCCAGGCCGCTGACTGGCGCTGACCTCAGGCTGACGTGGTCCTGCCCTGGGAGAGGCGGTGAACACACCTGCACAGGT... | CAGGAACTCAGGTCTTAGACTCTGGGGCTCGGCAGGGTACAGGGAAGAAATTCAGCTTCTCTGCCCCACCCCAACACGAGCAAGGTGGTCTGCCTCCATTTCCCTGCTTTCTTCAAAGTTGGCCCAAGTCCAGGGACAGCGTGTGGGTCGGAAGGTGACTAGCCCCAGCCCTCGCTGGAGGGGACTGTGCTCGCCACCATACTTCTTGTTCTGTTTCTGGGGTCAGGTTGACTGGATTCAAGTCCAGGCCGCTGACTGGCGCTGACCTCAGGCTGACGTGGTCCTGCCCTGGGAGAGGCGGTGAACACACCTGCACAGGT... |
Task1_train_46711 | Chromosome 19 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TTTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCATGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGTGCCTGGCCAATAATAATTTTTTAAAAATTAGGCTGGACGTGGTGGCTCACGTCTGTAATCCCAGCACTTTGGGAGGCCGAGACGGGCGGATCAGCCTGAGGTCAGGAGTTTGAGAGCAGCCTGGCCAACATGGTGAAACCCTGTCACTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGTGCACGCCTGTAAT... | TTTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCATGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGTGCCTGGCCAATAATAATTTTTTAAAAATTAGGCTGGACGTGGTGGCTCACGTCTGTAATCCCAGCACTTTGGGAGGCCGAGACGGGCGGATCAGCCTGAGGTCAGGAGTTTGAGAGCAGCCTGGCCAACATGGTGAAACCCTGTCACTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGTGCACGCCTGTAAT... |
Task1_train_46712 | Chromosome 19 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TGAAGTGGGAGGATCACTTGAACCTAGGAGGTCGAGGCTGCAGTGAGCTGTCATCGCGCCACTGCACTCTAGCCTGGGTGACAGAGCAAGACCCTATCTCAAAAATAAACACAAACAGCTTTATTGAGTGACTGCTTTTCCTCCCTATGAGCATTTTTTGGAACCTATCGTGTGTCAGGCCCTTGTGCCCAAGCCCCTGTTCAATCCCCGCATCAACCTCGTTAGGATTCTCACATTTTGCAGATGGGACACTAAGACTCTCAGAGGTCCAGCCCTCCAAAATACTGAAGTCCTAGTTCCGCTGGATTGAAAATGGGCAA... | TGAAGTGGGAGGATCACTTGAACCTAGGAGGTCGAGGCTGCAGTGAGCTGTCATCGCGCCACTGCACTCTAGCCTGGGTGACAGAGCAAGACCCTATCTCAAAAATAAACACAAACAGCTTTATTGAGTGACTGCTTTTCCTCCCTATGAGCATTTTTTGGAACCTATCGTGTGTCAGGCCCTTGTGCCCAAGCCCCTGTTCAATCCCCGCATCAACCTCGTTAGGATTCTCACATTTTGCAGATGGGACACTAAGACTCTCAGAGGTCCAGCCCTCCAAAATACTGAAGTCCTAGTTCCGCTGGATTGAAAATGGGCAA... |
Task1_train_46713 | This variant is present on Chromosome 19. Is the change likely to result in a pathogenic outcome? | Benign | TATTGAGTGACTGCTTTTCCTCCCTATGAGCATTTTTTGGAACCTATCGTGTGTCAGGCCCTTGTGCCCAAGCCCCTGTTCAATCCCCGCATCAACCTCGTTAGGATTCTCACATTTTGCAGATGGGACACTAAGACTCTCAGAGGTCCAGCCCTCCAAAATACTGAAGTCCTAGTTCCGCTGGATTGAAAATGGGCAACGCAGAACGGGGACTGGAAATTTTTTAAAAATTGTTTTTAAAGACGGGGTCTTGGCCAGGCGCAGTGGCTCACGGCTGTAATCTCAGCACTTTGGGAGGCCGAGGTGGGCGGATCACAAGG... | TATTGAGTGACTGCTTTTCCTCCCTATGAGCATTTTTTGGAACCTATCGTGTGTCAGGCCCTTGTGCCCAAGCCCCTGTTCAATCCCCGCATCAACCTCGTTAGGATTCTCACATTTTGCAGATGGGACACTAAGACTCTCAGAGGTCCAGCCCTCCAAAATACTGAAGTCCTAGTTCCGCTGGATTGAAAATGGGCAACGCAGAACGGGGACTGGAAATTTTTTAAAAATTGTTTTTAAAGACGGGGTCTTGGCCAGGCGCAGTGGCTCACGGCTGTAATCTCAGCACTTTGGGAGGCCGAGGTGGGCGGATCACAAGG... |
Task1_train_46714 | Here is a variant on Chromosome 19. Please identify whether it is a benign mutation or associated with a disorder. | Benign | AAAACTCCGTCTCAAAAATAAATAAATAAATAAAACAAAGACAAGGTCTCCGCCTGTAATCCTAGCACTTTGGGAGGCCGAGGCGGGCGGATCACCTGAGATCAGGAGCTCAAGACCAGCCTGGACAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGAGAGTGGTGGCACATGCCTGTAATCCCAGCTACTTGGGAGGCCGAGGCAGAATAGCTTGAACCTGGGAGGCAAATGTTGCAGTGAGCCCAGATTGCGCCACTGCACTCCAGCCTGGGCGACAGGGTAAGATCCGGCTCAAAAAAAAAAA... | AAAACTCCGTCTCAAAAATAAATAAATAAATAAAACAAAGACAAGGTCTCCGCCTGTAATCCTAGCACTTTGGGAGGCCGAGGCGGGCGGATCACCTGAGATCAGGAGCTCAAGACCAGCCTGGACAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGAGAGTGGTGGCACATGCCTGTAATCCCAGCTACTTGGGAGGCCGAGGCAGAATAGCTTGAACCTGGGAGGCAAATGTTGCAGTGAGCCCAGATTGCGCCACTGCACTCCAGCCTGGGCGACAGGGTAAGATCCGGCTCAAAAAAAAAAA... |
Task1_train_46715 | Assess the clinical impact of this variant found on Chromosome 19. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TGCATCCTCGAACTTCCGGGCTCAAGAGATTCTACCAACTCAGCCTCCCAAGTAGCTGGGACCACAGGTGCAAGCCACCCACGCCCGGCTAGTTTTTTGTATTTTTTTGTAGGGACTGGGTTTATCCAAGTTGCCCAGGCTGGTCTCGAACCCCAGAGCTCAAGCAACCCTCCTGCCTGGGCCTCCCGAAGTGCTGGGATTACAGGTGTGAGCCACCGTGCCCGGCCTAAGCCTCTCATAAGGCCGTGCTCCCTGCCAGAGGCCACCCTTGAAGAAGATTCCCTGAGACTTAATGACCTGGGGCACCCCGGACTTTCTTA... | TGCATCCTCGAACTTCCGGGCTCAAGAGATTCTACCAACTCAGCCTCCCAAGTAGCTGGGACCACAGGTGCAAGCCACCCACGCCCGGCTAGTTTTTTGTATTTTTTTGTAGGGACTGGGTTTATCCAAGTTGCCCAGGCTGGTCTCGAACCCCAGAGCTCAAGCAACCCTCCTGCCTGGGCCTCCCGAAGTGCTGGGATTACAGGTGTGAGCCACCGTGCCCGGCCTAAGCCTCTCATAAGGCCGTGCTCCCTGCCAGAGGCCACCCTTGAAGAAGATTCCCTGAGACTTAATGACCTGGGGCACCCCGGACTTTCTTA... |
Task1_train_46716 | This sequence change occurs on Chromosome 19. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TGGCACACCCGGTGGCATCCTCCCACCCGGGCTCTTATCGGCGGTCCCAGACCCTGCTTGAGCGCCTCCGGGTGTCAAGGGCCCCTGAGGACACTAAAGCTCTCGAACCCCGATGTGGACCCCCGTGCGGCGCGGGGCAGCCTGGCTGGGAACCCTGCTCGGCCCTGGAGAGGGGCCCCCCGAGCCGAGGGGAGGAGCGGCGCATGCCCACAAGCCCCCCGCGGGAAGTAGGAAATCGACCGACCAGGCGGTGCGCTTCGGACCCAGCCAGGGCATGTGCTCGGAGGCCCGCCTGGCTCGCAGGTTGCGGGATGCGCTGC... | TGGCACACCCGGTGGCATCCTCCCACCCGGGCTCTTATCGGCGGTCCCAGACCCTGCTTGAGCGCCTCCGGGTGTCAAGGGCCCCTGAGGACACTAAAGCTCTCGAACCCCGATGTGGACCCCCGTGCGGCGCGGGGCAGCCTGGCTGGGAACCCTGCTCGGCCCTGGAGAGGGGCCCCCCGAGCCGAGGGGAGGAGCGGCGCATGCCCACAAGCCCCCCGCGGGAAGTAGGAAATCGACCGACCAGGCGGTGCGCTTCGGACCCAGCCAGGGCATGTGCTCGGAGGCCCGCCTGGCTCGCAGGTTGCGGGATGCGCTGC... |
Task1_train_46717 | A variant on Chromosome 19 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GGCACCCGCGCGGCCTGCGTTGCCTCGGGGCCCTACTGCGCCAAGGCGGGGACCCCAACGCTCGGTAAGATAGAGCCTGGGTCCGGGGCGGGGTCTCCCCAAGCCGAAGTCTGGGAATCCGGGAAGGGGCGCCCCATCATCCCGGGCCAGGCCTCGGGGCTCGAGGGTGGGGTTTAGGGGATCTTGGGGAGGGAACTTGGGGGTCCAAGGGCAGGGGCTAGGGCTCGAGGGAGGCGCTGGGGTCCCAGACCGAGGGCGTGGAATGGGGCTGCGCTAGGACCAAAGTGGGGATCAAGGGTTCGGATATTGGAGTGGAGGCA... | GGCACCCGCGCGGCCTGCGTTGCCTCGGGGCCCTACTGCGCCAAGGCGGGGACCCCAACGCTCGGTAAGATAGAGCCTGGGTCCGGGGCGGGGTCTCCCCAAGCCGAAGTCTGGGAATCCGGGAAGGGGCGCCCCATCATCCCGGGCCAGGCCTCGGGGCTCGAGGGTGGGGTTTAGGGGATCTTGGGGAGGGAACTTGGGGGTCCAAGGGCAGGGGCTAGGGCTCGAGGGAGGCGCTGGGGTCCCAGACCGAGGGCGTGGAATGGGGCTGCGCTAGGACCAAAGTGGGGATCAAGGGTTCGGATATTGGAGTGGAGGCA... |
Task1_train_46718 | This variant lies on Chromosome 19. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TTTTTTATTTTTTTAAGACGGAGTTTCACTCTTGTTGCCAAGGCAGGAGTACAATGGTGCCGTCTCGGCTCACTGCAACCTCCACCTCCCAGGTTCAAACAATCCTCTTGTCTCAGCCTCTCAAGTAGCTGGGATTACAAGCACCTGCCACCACGCCCGACTAATTTTTGTATTTTTAGTAGAGACGAGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTAATCCACCCACCCTGGCCTCCCAAAATGCTGGGACTACAGGTGTGAGCCACCGCACCGGCCTCTTTTTTTTTTTTTTTTTTTGAG... | TTTTTTATTTTTTTAAGACGGAGTTTCACTCTTGTTGCCAAGGCAGGAGTACAATGGTGCCGTCTCGGCTCACTGCAACCTCCACCTCCCAGGTTCAAACAATCCTCTTGTCTCAGCCTCTCAAGTAGCTGGGATTACAAGCACCTGCCACCACGCCCGACTAATTTTTGTATTTTTAGTAGAGACGAGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTAATCCACCCACCCTGGCCTCCCAAAATGCTGGGACTACAGGTGTGAGCCACCGCACCGGCCTCTTTTTTTTTTTTTTTTTTTGAG... |
Task1_train_46719 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | ACCATCCTGGCTAACACGGTGAAACCCCGTCTGTACTAAAAAGACAAAAAATTAGCCAGGCATGGTAGCGGGTGCCTGTAGTCCCAGCTACTAGGGAGGCTGAGGCAGGAGAATGGCATGAACCTGGGAGGTGGAGCTTGCAGTGAGCCAGGATCACGCCACTGCACTCCAGCCTGGGGGACAGAGTGAGACTCCATCTCAAAAAAAAAAAAAAAAAAAAAAATTAAGGCTGAGCACAATGACTCACACCTGTAGTCCTAGCACTTTGGGAGGCTGAGGTGCAAGGATCACTTGAGCCCAGTAGTTAAAGAACATCTTGG... | ACCATCCTGGCTAACACGGTGAAACCCCGTCTGTACTAAAAAGACAAAAAATTAGCCAGGCATGGTAGCGGGTGCCTGTAGTCCCAGCTACTAGGGAGGCTGAGGCAGGAGAATGGCATGAACCTGGGAGGTGGAGCTTGCAGTGAGCCAGGATCACGCCACTGCACTCCAGCCTGGGGGACAGAGTGAGACTCCATCTCAAAAAAAAAAAAAAAAAAAAAAATTAAGGCTGAGCACAATGACTCACACCTGTAGTCCTAGCACTTTGGGAGGCTGAGGTGCAAGGATCACTTGAGCCCAGTAGTTAAAGAACATCTTGG... |
Task1_train_46720 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | ATCCCAGCTCTGTGGTACCGGCGGGGCCATGGTAGGCCCTCAGGAGAGCTCAGGTCTCAAATCCAGCCTCTGCCCTTTGCTGATGTGTGACCTCGGGCAAGTTACTTCACTTTCCTGAGCCTCCGTTTATTTCTCTATGAAATTAATCCTCTCATAAGTTTGCTACGCAGGTAAAGCACTCATCATAGTGTCGTGCATATAACAAATGCTCCATATATTATGGGCATTATTATAGTGGTGATGTTTTGCTAAACGATGCTACAGGTAGGATGGGCTTCGGAGGACGAGGGGTTAAATGCTCCTTGCTGCTTGGCCACTCA... | ATCCCAGCTCTGTGGTACCGGCGGGGCCATGGTAGGCCCTCAGGAGAGCTCAGGTCTCAAATCCAGCCTCTGCCCTTTGCTGATGTGTGACCTCGGGCAAGTTACTTCACTTTCCTGAGCCTCCGTTTATTTCTCTATGAAATTAATCCTCTCATAAGTTTGCTACGCAGGTAAAGCACTCATCATAGTGTCGTGCATATAACAAATGCTCCATATATTATGGGCATTATTATAGTGGTGATGTTTTGCTAAACGATGCTACAGGTAGGATGGGCTTCGGAGGACGAGGGGTTAAATGCTCCTTGCTGCTTGGCCACTCA... |
Task1_train_46721 | A variant on Chromosome 19 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TCCATGCACTCCAGCCTGGATGACAGAGTGAGAGAGATTCTGTCTCAAAGAAAAAACAAAAACAAAAACAAAAAGGACTATGGCTGCAGCAGACTATACCCAGGTAGCCACGCGAGGCTCTGTTCAATAAAATAAAAATTCAGTTTCTCGGTCGCAGCAGCTGCACTTCAACGTGCTCACTTATCACCTGTAGCTAAAGGCTGCAGGGACAGTGCAGACAAAGGACATTGTCATCCTCGAGGAATGTTCCCTGTGCAGGCACTGGGGAGCTCCTTGGCCCATTCTGTAGCTTTCTGAGGAATGCGGAAGAAGCTGCGCTT... | TCCATGCACTCCAGCCTGGATGACAGAGTGAGAGAGATTCTGTCTCAAAGAAAAAACAAAAACAAAAACAAAAAGGACTATGGCTGCAGCAGACTATACCCAGGTAGCCACGCGAGGCTCTGTTCAATAAAATAAAAATTCAGTTTCTCGGTCGCAGCAGCTGCACTTCAACGTGCTCACTTATCACCTGTAGCTAAAGGCTGCAGGGACAGTGCAGACAAAGGACATTGTCATCCTCGAGGAATGTTCCCTGTGCAGGCACTGGGGAGCTCCTTGGCCCATTCTGTAGCTTTCTGAGGAATGCGGAAGAAGCTGCGCTT... |
Task1_train_46722 | Consider this mutation on Chromosome 19. Is this a benign change or a disease-causing variant? | Benign | TGTAGTCCCTCCTTTCTTGAACGGGAAAACTGAACGCACATAGGTCCTTGCCACGCCTAAGGCTGCGGAGTGAGCAGATGGAAAATGCGGGACTCAAAACCTCCCCTCGCTGTAATTTGCACTGCCCTGTGCCAAACTCTGTCCTTTCTTCCATTCCTTATTCCTATTGTCAGCCTCGCTGCGCTAGGACCCTAAAAATTTGGTCTCATGTTGCCCGGGGAACAACATTTCGCTACACCTACCTCCATACCGCCTCCCGCTCCCGCTCTCCCTTGCACCAGCCAATGGAAGCGAGTATCTTCAGACGGTGGGCAGGACGT... | TGTAGTCCCTCCTTTCTTGAACGGGAAAACTGAACGCACATAGGTCCTTGCCACGCCTAAGGCTGCGGAGTGAGCAGATGGAAAATGCGGGACTCAAAACCTCCCCTCGCTGTAATTTGCACTGCCCTGTGCCAAACTCTGTCCTTTCTTCCATTCCTTATTCCTATTGTCAGCCTCGCTGCGCTAGGACCCTAAAAATTTGGTCTCATGTTGCCCGGGGAACAACATTTCGCTACACCTACCTCCATACCGCCTCCCGCTCCCGCTCTCCCTTGCACCAGCCAATGGAAGCGAGTATCTTCAGACGGTGGGCAGGACGT... |
Task1_train_46723 | A mutation on Chromosome 19 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CTGGCCCTTTTGGGGACAGTGAGAAGCCACCTGCGACCCTGTGTCCTGAGCTTTGTGTGGAATGTCCTTTGGGGCCTTGTAGTTGTAAAATACAGAAGTGGCTTCTGAAGCCTGGGGCACCGAGTGGTGACAGCTGCCTGCCTGGAGGGAGATCTCTGCCCAGGTCCAACGCCACCAACCCTAAGCCACCAGAAAGTGGAGAGTGCTGAGCTCTGCGGTCAGATTCAAGTTCCACTTTCAGCTCCATCTGGGACTAGCTGATGGGATTTCAAACCAACAAAGTTAGCCGGGCGTCGTGGCTCACGCCTGTAATCTCAGCA... | CTGGCCCTTTTGGGGACAGTGAGAAGCCACCTGCGACCCTGTGTCCTGAGCTTTGTGTGGAATGTCCTTTGGGGCCTTGTAGTTGTAAAATACAGAAGTGGCTTCTGAAGCCTGGGGCACCGAGTGGTGACAGCTGCCTGCCTGGAGGGAGATCTCTGCCCAGGTCCAACGCCACCAACCCTAAGCCACCAGAAAGTGGAGAGTGCTGAGCTCTGCGGTCAGATTCAAGTTCCACTTTCAGCTCCATCTGGGACTAGCTGATGGGATTTCAAACCAACAAAGTTAGCCGGGCGTCGTGGCTCACGCCTGTAATCTCAGCA... |
Task1_train_46724 | Here is a genetic alteration on Chromosome 19. Based on the data, is it a benign variant or a cause of disease? | Benign | GTTCTAGATCGGAGTTTTTGATTTCTGTATTCTGCCGTGTTCCCTGGTAATGCCCCAGTCCACGAGCAACAGAGGGAGACCTGGGAGACTCTTGGCTCCTGCTGGCAGCCCGGGACCCCCAGCCCACGTGGTATCAAATATTGAAATGCATCCGTGTAACATATAAATCTGTTGTTAAAGGATTGTTGTGATTTTGCGCATGAAATATGTGGGCAACTCGGCCGGACGCGATGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCAGATCACCTGAGATCGGGAGTTCGAGACCAGCCTGACCAACATG... | GTTCTAGATCGGAGTTTTTGATTTCTGTATTCTGCCGTGTTCCCTGGTAATGCCCCAGTCCACGAGCAACAGAGGGAGACCTGGGAGACTCTTGGCTCCTGCTGGCAGCCCGGGACCCCCAGCCCACGTGGTATCAAATATTGAAATGCATCCGTGTAACATATAAATCTGTTGTTAAAGGATTGTTGTGATTTTGCGCATGAAATATGTGGGCAACTCGGCCGGACGCGATGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCAGATCACCTGAGATCGGGAGTTCGAGACCAGCCTGACCAACATG... |
Task1_train_46725 | A mutation on Chromosome 19 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GGGCAGGGCCAGGTACTACAACAAACACACCCCACATTCCAGTGGCTTACCCCAGTACAAGGTTATTGGTTCCCAGAGCCAGGGGCGCAGGGTGGTGGGGCAGGGAGCCAGGAAGGGGTGGGGACCACTCATTTCTCCAGCTTCTCAACCAAGAAAATCTGAATTTCCAGCTTCTGTGATCTAAACTTTTCCTTTCCTTTCCATTTCCTTTTTGTTTCCTTTTTTTTTTTTTTTTTTGATGGAGTCTTGCTCTTTGGCCCAGGCTGGAGTGAATTTGCGTGATCTCGGCTCACTGCAACCTCTGCCTGCTGTGTTTAAGC... | GGGCAGGGCCAGGTACTACAACAAACACACCCCACATTCCAGTGGCTTACCCCAGTACAAGGTTATTGGTTCCCAGAGCCAGGGGCGCAGGGTGGTGGGGCAGGGAGCCAGGAAGGGGTGGGGACCACTCATTTCTCCAGCTTCTCAACCAAGAAAATCTGAATTTCCAGCTTCTGTGATCTAAACTTTTCCTTTCCTTTCCATTTCCTTTTTGTTTCCTTTTTTTTTTTTTTTTTTGATGGAGTCTTGCTCTTTGGCCCAGGCTGGAGTGAATTTGCGTGATCTCGGCTCACTGCAACCTCTGCCTGCTGTGTTTAAGC... |
Task1_train_46726 | A variant found on Chromosome 19 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | TCAGGAGACCATACTCAGGAAGAGCCTGACTCCCTCTTGGAAGTGCCTGTGAGCTTCCCGCTGTTCCTGCAGCACCCCTTCCGCCGGCACCTCTGCTTCTCTGCAGCCACCAGGGAGGCACAGCATGCCTGGAGGCTGGCCCTGCAGGGTGGCATCCGGCTTCAGGGCATAGGTGGGTCTCAGGACGGGTCAGACATTTGTGGGGCTAATGGTCTGGGGTCAGATGGCTCAGCCTCTGTTGGCTCGGGACCTCTCCAGGCCTCACTTTCTTTACCCAGAAAATGGGTTTTTAGGCCAGGTGTGGTGGTTCATGCCTGTAA... | TCAGGAGACCATACTCAGGAAGAGCCTGACTCCCTCTTGGAAGTGCCTGTGAGCTTCCCGCTGTTCCTGCAGCACCCCTTCCGCCGGCACCTCTGCTTCTCTGCAGCCACCAGGGAGGCACAGCATGCCTGGAGGCTGGCCCTGCAGGGTGGCATCCGGCTTCAGGGCATAGGTGGGTCTCAGGACGGGTCAGACATTTGTGGGGCTAATGGTCTGGGGTCAGATGGCTCAGCCTCTGTTGGCTCGGGACCTCTCCAGGCCTCACTTTCTTTACCCAGAAAATGGGTTTTTAGGCCAGGTGTGGTGGTTCATGCCTGTAA... |
Task1_train_46727 | This sequence variant lies on Chromosome 19. Is it clinically significant, and what condition might it cause if any? | Benign | CATTTCCTAATCACCTTCTCCAGGAACTGTCCCTGGTCCCCTCTATGTCTTGCAGTAGCCTGTGCTTCTCTTATCACAGCCTGACTTTCATACCACTGTGGGTGATTTCTATACTCTGTCTCCCCTAATTTGTAAGCAGAGACTGGGTTAGAGTATTCCATTTCTGCAGCCCCAGGGCCCAGCACAGACAGAACATGAGATGGTATTCACAGATCTGGGCCAGGAAATGTGCTCATTTCCTCTCAATTGTGCCAGCATCGCTTGTTATAGTTTTTTCAGGTTTTATCATTTTATGTCCATGACACCGTGCCTCACTGCTA... | CATTTCCTAATCACCTTCTCCAGGAACTGTCCCTGGTCCCCTCTATGTCTTGCAGTAGCCTGTGCTTCTCTTATCACAGCCTGACTTTCATACCACTGTGGGTGATTTCTATACTCTGTCTCCCCTAATTTGTAAGCAGAGACTGGGTTAGAGTATTCCATTTCTGCAGCCCCAGGGCCCAGCACAGACAGAACATGAGATGGTATTCACAGATCTGGGCCAGGAAATGTGCTCATTTCCTCTCAATTGTGCCAGCATCGCTTGTTATAGTTTTTTCAGGTTTTATCATTTTATGTCCATGACACCGTGCCTCACTGCTA... |
Task1_train_46728 | An alteration has been detected on Chromosome 19. Is it pathogenic, and if so, what disease is involved? | Benign | CTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCATGTGCCACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGCTGGTCTCAAACTCCTGACATCGTGATCCTCCCCCCTTGGGCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCACCCGGCCAAGACTCCATCTTTTATTTTTTATTTTATTTTTGAGACAGAGTCTCACTCTGTCACCCAGGCAGGAGTGCAATGGCATGGTCTCGGCTCACTGCAACCTCCGCCTCCTGG... | CTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCATGTGCCACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGCTGGTCTCAAACTCCTGACATCGTGATCCTCCCCCCTTGGGCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCACCCGGCCAAGACTCCATCTTTTATTTTTTATTTTATTTTTGAGACAGAGTCTCACTCTGTCACCCAGGCAGGAGTGCAATGGCATGGTCTCGGCTCACTGCAACCTCCGCCTCCTGG... |
Task1_train_46729 | A variant has been detected on Chromosome 19. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TGTGAGCTCAGCCCTGGGGGGCTGAGATTGTGGTGAATTTGTGTCCCATCTCTCTCTCTCTCTCTCTCTTTTTTTTTTTTTTGAGACAGAGTCTAGATCTGTTGCCCAGGCTGGAATGCATAATCTCAGCTCACTGCAACCTCCTCCTCCCAGGTTCAAGTGAATCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGGCACATGCCACCATGCCCAGCTAATTTTTGTATTTTTAATAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCACATGATCTGACTGCCTCAGCCTCC... | TGTGAGCTCAGCCCTGGGGGGCTGAGATTGTGGTGAATTTGTGTCCCATCTCTCTCTCTCTCTCTCTCTTTTTTTTTTTTTTGAGACAGAGTCTAGATCTGTTGCCCAGGCTGGAATGCATAATCTCAGCTCACTGCAACCTCCTCCTCCCAGGTTCAAGTGAATCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGGCACATGCCACCATGCCCAGCTAATTTTTGTATTTTTAATAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCACATGATCTGACTGCCTCAGCCTCC... |
Task1_train_46730 | This alteration occurs on Chromosome 19. Is it associated with a disease or is it a benign variant? | Benign | GGTCTCGATCTCCTGACCTCGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCTTGAGCAACCACGCCCGGCCATCACTTCTCCTTAAGTGTCATCTCCTCCAGGGAGTTTTCCTGATTGCCTTGGATTAGTTTTATGCTTTTCCTATGAAACCCAGAGAGCCTTCCATGTGTCTTTTTCTTGTCATATTACTAGTTCCATAGTTTGTTTTTCTTGTATATCACATAGTTCCAATAGTAGCTGCTATTTTTTCAATTTAATTTCTTGACCTAGTGGAAGTTATCCAACAGCCTTTTCACTGTGTCCTCT... | GGTCTCGATCTCCTGACCTCGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCTTGAGCAACCACGCCCGGCCATCACTTCTCCTTAAGTGTCATCTCCTCCAGGGAGTTTTCCTGATTGCCTTGGATTAGTTTTATGCTTTTCCTATGAAACCCAGAGAGCCTTCCATGTGTCTTTTTCTTGTCATATTACTAGTTCCATAGTTTGTTTTTCTTGTATATCACATAGTTCCAATAGTAGCTGCTATTTTTTCAATTTAATTTCTTGACCTAGTGGAAGTTATCCAACAGCCTTTTCACTGTGTCCTCT... |
Task1_train_46731 | This mutation occurs on Chromosome 19. Does this change lead to a known medical condition, or is it benign? | Benign | GAGAGGGGTGGTTATGTATCGACTCGAGGCTACCCCAAAGAGGACTGCTGGATACGTCACTGCACAGAACGGGTCCTTTAGTGTTCACCCCCTCCCTCAGCTCCGGAACCTTCTGTTGGACCCTGCCTCTCACAAGCTACTGGTGTTGGCTGGGCCCTGCCTGGAGGAGACGGGGGAGCTGCTGCTACAGACAGGGGGCTTCTCGCCTCACCACTTCCTCCAGGTCCTGAAGGACAGAGAGGTAAGCCACCCCTTTGCCATCCCCTGCTTCCCCAGCTCTGAATCCTGACTGGGGTGTATCAGGCTGTGTGGCACCAGCG... | GAGAGGGGTGGTTATGTATCGACTCGAGGCTACCCCAAAGAGGACTGCTGGATACGTCACTGCACAGAACGGGTCCTTTAGTGTTCACCCCCTCCCTCAGCTCCGGAACCTTCTGTTGGACCCTGCCTCTCACAAGCTACTGGTGTTGGCTGGGCCCTGCCTGGAGGAGACGGGGGAGCTGCTGCTACAGACAGGGGGCTTCTCGCCTCACCACTTCCTCCAGGTCCTGAAGGACAGAGAGGTAAGCCACCCCTTTGCCATCCCCTGCTTCCCCAGCTCTGAATCCTGACTGGGGTGTATCAGGCTGTGTGGCACCAGCG... |
Task1_train_46732 | This variant is present on Chromosome 19. Is the change likely to result in a pathogenic outcome? | Benign | CTGGGTTCAAGTCCTCTGGTAGCTGTTTCTCTGCGGGTGACCTCACTGCAGTTTTCTCTGGAGAGCCTCTGTTCCCTCATCTGTAAATAAGATAGAGGACCACTTCTGCCTCCTAAGGGTGCATTCAGGATTCAAGGTAGGGTAAGCACCAAGCACAGCGCCCGGCAACAAACAGATACCCAGCCTGTGTAGGTTACTGTAGGGGAAACTGAGGCTGAGGCGGGTAGGGGCCATGGCCTCTTAACATGCTGTGTTCTGAAAACACAAAAGTGGCTAGGCACAGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCTG... | CTGGGTTCAAGTCCTCTGGTAGCTGTTTCTCTGCGGGTGACCTCACTGCAGTTTTCTCTGGAGAGCCTCTGTTCCCTCATCTGTAAATAAGATAGAGGACCACTTCTGCCTCCTAAGGGTGCATTCAGGATTCAAGGTAGGGTAAGCACCAAGCACAGCGCCCGGCAACAAACAGATACCCAGCCTGTGTAGGTTACTGTAGGGGAAACTGAGGCTGAGGCGGGTAGGGGCCATGGCCTCTTAACATGCTGTGTTCTGAAAACACAAAAGTGGCTAGGCACAGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCTG... |
Task1_train_46733 | Here is a variant on Chromosome 19. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGGGCACGCCACCATGCCCGGCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTGGCGAGGCTGGTCTGGAACTCCTGACCTCGAGTGATCCTCCTGCCTCGGACTCCCAAAGTGCTGGGATTACCGGCGTGAGAAACTGCGCCTGGCCTAATGAGGTTTAAGACAATCAGAGGACTAGGACCCCTAGGACTCAGCTTTCGCAGCTGTGAAATGGGCTGACTCCCCAGCATCCTCATTGAGGTGGTCTGCTGAGCGCAATCCAGGCCTAAA... | TGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGGGCACGCCACCATGCCCGGCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTGGCGAGGCTGGTCTGGAACTCCTGACCTCGAGTGATCCTCCTGCCTCGGACTCCCAAAGTGCTGGGATTACCGGCGTGAGAAACTGCGCCTGGCCTAATGAGGTTTAAGACAATCAGAGGACTAGGACCCCTAGGACTCAGCTTTCGCAGCTGTGAAATGGGCTGACTCCCCAGCATCCTCATTGAGGTGGTCTGCTGAGCGCAATCCAGGCCTAAA... |
Task1_train_46734 | A genomic variant on Chromosome 19 is under review. What is the biological outcome — benign or pathogenic? | Benign | AAAACCTGGACTTGGTGGAAGGGACTCCATGGAGGAGCCATGGGGACGTCAGGAGGAGGGGTTATTTGGTGACATCCAGGGGTCAGAGAGACCCTTCAGGGGTGGGCTACAGGGGAGGGTTCCAGACACAAGTAGAATCAGAAAGGTCCCTGGAGGCCATGGGCTTGGGTGCTGGGAGCAACAGGCATTTACTTGGCAGATGCTGAGCCCTGGGTGGGGCGAGGAGGCCTGGCTCCTGGGGAGACGACGCTGTGCATAGCCGAGGAGCCCCAGGTCCTGGCAGCCTCTGATAAGGCCATCCATCGCCTGGCTCAACGAGA... | AAAACCTGGACTTGGTGGAAGGGACTCCATGGAGGAGCCATGGGGACGTCAGGAGGAGGGGTTATTTGGTGACATCCAGGGGTCAGAGAGACCCTTCAGGGGTGGGCTACAGGGGAGGGTTCCAGACACAAGTAGAATCAGAAAGGTCCCTGGAGGCCATGGGCTTGGGTGCTGGGAGCAACAGGCATTTACTTGGCAGATGCTGAGCCCTGGGTGGGGCGAGGAGGCCTGGCTCCTGGGGAGACGACGCTGTGCATAGCCGAGGAGCCCCAGGTCCTGGCAGCCTCTGATAAGGCCATCCATCGCCTGGCTCAACGAGA... |
Task1_train_46735 | A variant on Chromosome 19 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | AGGTTGCAGTGAGCCGAGATGGCAGCAGCACAGTCCAGCTTCTGCTCGGCATGAGAGGGAGACCGTGGAAAGAGAGGGAGAGGGAGACCAAGGGGAGAGGGAGAGGGAGAGGGAGCTTAAAAATTGTTAAATTGTTATACATTTAAGGAAAAAACAGTGACACTGGAGGGGCGAGGCCAGTGGAGGTGCTGTGTGACCTCGGGCAGAGCCCCACCCATCTCTGGGCCTTTGGGGTCCGTCTGCGAAATGAATTGAGGGAGGCGCTGGCTCAGTAGTCCCTTCAGGGTTACCTAATCCCGCTTCTCCTCCCGGACTTAACG... | AGGTTGCAGTGAGCCGAGATGGCAGCAGCACAGTCCAGCTTCTGCTCGGCATGAGAGGGAGACCGTGGAAAGAGAGGGAGAGGGAGACCAAGGGGAGAGGGAGAGGGAGAGGGAGCTTAAAAATTGTTAAATTGTTATACATTTAAGGAAAAAACAGTGACACTGGAGGGGCGAGGCCAGTGGAGGTGCTGTGTGACCTCGGGCAGAGCCCCACCCATCTCTGGGCCTTTGGGGTCCGTCTGCGAAATGAATTGAGGGAGGCGCTGGCTCAGTAGTCCCTTCAGGGTTACCTAATCCCGCTTCTCCTCCCGGACTTAACG... |
Task1_train_46736 | This sequence change occurs on Chromosome 19. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GGCATTTGAGACCAGCCTGGCCAACATGCTAAAACCCTGTCTCTACTAAAGATACAAAAAATTATCCAGGCATGGTAGTGCACACCTATAATCCCAGCTACTCAGGAGGCTGAGGAAGGAGAATGGCTTGAACCCGGGAGGCAGAGGTTGTATGATTGCAGTGGTGCAATCATAGCTCACTGCAGCCTCAAACTCCTGGGATCAAGTGATCTTACCACCTCAGCCTCCTGAGTAGTTGGGACTACAGGCACATGCCACCATGGCTGGCAAACTTTTTTCTTTCTGTAGAGACGGGGTCTTGCTATGTTGCCCAGGCTGTT... | GGCATTTGAGACCAGCCTGGCCAACATGCTAAAACCCTGTCTCTACTAAAGATACAAAAAATTATCCAGGCATGGTAGTGCACACCTATAATCCCAGCTACTCAGGAGGCTGAGGAAGGAGAATGGCTTGAACCCGGGAGGCAGAGGTTGTATGATTGCAGTGGTGCAATCATAGCTCACTGCAGCCTCAAACTCCTGGGATCAAGTGATCTTACCACCTCAGCCTCCTGAGTAGTTGGGACTACAGGCACATGCCACCATGGCTGGCAAACTTTTTTCTTTCTGTAGAGACGGGGTCTTGCTATGTTGCCCAGGCTGTT... |
Task1_train_46737 | An alteration has been detected on Chromosome 19. Is it pathogenic, and if so, what disease is involved? | Benign | CACGCCCAGCCCCATTTTATTTTATTTTTTAGAGATGGGGTCTCACTATGTTGCCCGGGCTGGTCTCAAACCACTGGCCTCAAGTGATCCTCCCGCCTCAGCCTTCTGAGCAGCTGGAACTACAGGTGTGCACCACCACCTCCGGCTGTTGCCTTATTTCTAATGCTTGCCCCTGTTCCTGTACTCAGAGTGATCTTACCAGGGGGAACGCACACGGGGCTGCTCCACTTGCTCCAGGAACTTCCTTGGCTCCCCAGCTGCCGTCGTCGGAGCTGGAATTCCTGGGCCACATTCATCTCCAGGGGGCAGAGGCAGGACTC... | CACGCCCAGCCCCATTTTATTTTATTTTTTAGAGATGGGGTCTCACTATGTTGCCCGGGCTGGTCTCAAACCACTGGCCTCAAGTGATCCTCCCGCCTCAGCCTTCTGAGCAGCTGGAACTACAGGTGTGCACCACCACCTCCGGCTGTTGCCTTATTTCTAATGCTTGCCCCTGTTCCTGTACTCAGAGTGATCTTACCAGGGGGAACGCACACGGGGCTGCTCCACTTGCTCCAGGAACTTCCTTGGCTCCCCAGCTGCCGTCGTCGGAGCTGGAATTCCTGGGCCACATTCATCTCCAGGGGGCAGAGGCAGGACTC... |
Task1_train_46738 | Chromosome 19 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CACCCTTTAGTCCTCAGAGGTTGAGATGCATATTTGGGAGACACTCTCGGGAGGTACCCCTGCAGGAAAGAACAGTAAGACCAACAGTCTGGAGGGCAGAGAGAAGTGGAGGTGTGCCTGGGGTGGCACCAGTGTCTGAAGCCAGCATGGGGAAAGACAGTAGAGGGTGCATGGCAGGGAGAGGCCTGCCAGGGCTGGCCCAGGCAAGCACACTTGGCCCACTAGCAGTCAGGGCAATTATTAATAACATTTCTCCAGGAGGCAGCGACCTCCCTCAGCCACTGGGATCCCCGTGCCCTTTGGGATTGCCACAGTCTGCT... | CACCCTTTAGTCCTCAGAGGTTGAGATGCATATTTGGGAGACACTCTCGGGAGGTACCCCTGCAGGAAAGAACAGTAAGACCAACAGTCTGGAGGGCAGAGAGAAGTGGAGGTGTGCCTGGGGTGGCACCAGTGTCTGAAGCCAGCATGGGGAAAGACAGTAGAGGGTGCATGGCAGGGAGAGGCCTGCCAGGGCTGGCCCAGGCAAGCACACTTGGCCCACTAGCAGTCAGGGCAATTATTAATAACATTTCTCCAGGAGGCAGCGACCTCCCTCAGCCACTGGGATCCCCGTGCCCTTTGGGATTGCCACAGTCTGCT... |
Task1_train_46739 | A mutation is present on Chromosome 19. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GCCACCACACCCGGCTAATTTTTATATTTTTAGTAGAGACGGGGTTTTGCCATGTTAGCCAGGATGGTCTCGGTCTCCTGACCTCGTGATCCGCCCTCCTCAACCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCAATGTGCCCGGCCTTTTTTTTTTTTCTTTTTTTAAGAGACTGGTTCTCACTCTGTCTCCCAGACTGGAGTGCAGTGGCACGATCATAGCTCACTTCAGCCTCAGACTCCTGGGCTCAAGAGATCCTCTCAAGTAGCTGGGACTACAGGCGTGCACCACGGCACCCGGCTAATTTTTTAAGCAAT... | GCCACCACACCCGGCTAATTTTTATATTTTTAGTAGAGACGGGGTTTTGCCATGTTAGCCAGGATGGTCTCGGTCTCCTGACCTCGTGATCCGCCCTCCTCAACCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCAATGTGCCCGGCCTTTTTTTTTTTTCTTTTTTTAAGAGACTGGTTCTCACTCTGTCTCCCAGACTGGAGTGCAGTGGCACGATCATAGCTCACTTCAGCCTCAGACTCCTGGGCTCAAGAGATCCTCTCAAGTAGCTGGGACTACAGGCGTGCACCACGGCACCCGGCTAATTTTTTAAGCAAT... |
Task1_train_46740 | A sequence alteration has been identified on Chromosome 19. Is it disease-inducing or harmless? | Benign | AAAAAATGTAAGAAACACCTTTAGCTCATCATGAGCAGCACAAAACAGGCAGGGACAGGATTTGGCCCTGAGGCAGGAGAATAGGTCTGGAGGCAGGGAACATAAGGCCAAATCAAATGGAAACAATTCAGCTATGACAGGAAATATCTTCTCCATTTAAAGAGGGCATACATCCAGTAAATGACTTTGTAACTTTACTTCATCCTCTTCATTTACATAGGACGTACATTAAGTAACCAGTGAAAACCTCTAGAGGGCATTTAAACCCCAGAAAATTCTTAAACAGGTCTCTTGAGTCCGTATGCTCCACTGGCTCCCAC... | AAAAAATGTAAGAAACACCTTTAGCTCATCATGAGCAGCACAAAACAGGCAGGGACAGGATTTGGCCCTGAGGCAGGAGAATAGGTCTGGAGGCAGGGAACATAAGGCCAAATCAAATGGAAACAATTCAGCTATGACAGGAAATATCTTCTCCATTTAAAGAGGGCATACATCCAGTAAATGACTTTGTAACTTTACTTCATCCTCTTCATTTACATAGGACGTACATTAAGTAACCAGTGAAAACCTCTAGAGGGCATTTAAACCCCAGAAAATTCTTAAACAGGTCTCTTGAGTCCGTATGCTCCACTGGCTCCCAC... |
Task1_train_46741 | This variant is located on Chromosome 19. Evaluate its biological effect and specify any disease association. | Benign | ATCCACCCGCCCCACCCACTCTACCCAAAAGCAGCTTTTGGAAATCCTTAGCAAACTCCTACCCATGCGTTGAAGGCCCAACTCTAGCATGCCCTCCTGTAAGAAACCATCCAGGTCCCTGGCGCTTCCCTGACTGCAGGGCTAGGGTTGTCTGTGTTTGGCTCTGCCTACCCAAGACTGGGAAGGCTCCTCATGGACCCCCTATGGCCAGTGACAGTGAGTACTCAGTAATGTTTTTTTTTTTTCTTTTTCTTTTTTAGAGACAGGGTCTTGCTGTCACCCAGGCTGGAGTGCAGTGGTGCAATCACGGTTCCCTGCAG... | ATCCACCCGCCCCACCCACTCTACCCAAAAGCAGCTTTTGGAAATCCTTAGCAAACTCCTACCCATGCGTTGAAGGCCCAACTCTAGCATGCCCTCCTGTAAGAAACCATCCAGGTCCCTGGCGCTTCCCTGACTGCAGGGCTAGGGTTGTCTGTGTTTGGCTCTGCCTACCCAAGACTGGGAAGGCTCCTCATGGACCCCCTATGGCCAGTGACAGTGAGTACTCAGTAATGTTTTTTTTTTTTCTTTTTCTTTTTTAGAGACAGGGTCTTGCTGTCACCCAGGCTGGAGTGCAGTGGTGCAATCACGGTTCCCTGCAG... |
Task1_train_46742 | This variant lies on Chromosome 19. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AGTGTCCAAGAGGGCCTGAGGGGACGAGAGAGTGGCCAAGAGGGTGGCCGGGCATGGAGGGGGAGGGGCGGGGAGGGCAGAGGAAGGAGGGGGGAAGGAGGGAAGGGAGGCGTAGGAGTGAGGAGGCTGGGTGAGAGGTGTTAAGATTAATTGTTCATGTGTTTGCATATGATAGAGTGAGAGAGAGGGCGCGAAGGAAGATGGTGGTAGGGGACCAGCAGCTCTGGGAAGGGGGGGATTTTATCAACTCAGGGTCTAGGATATCTGCTTCCAAGCAGAGCCCATGGGGTGTGGCCTAAGGAGCTTGGGGGCTCCAGGAA... | AGTGTCCAAGAGGGCCTGAGGGGACGAGAGAGTGGCCAAGAGGGTGGCCGGGCATGGAGGGGGAGGGGCGGGGAGGGCAGAGGAAGGAGGGGGGAAGGAGGGAAGGGAGGCGTAGGAGTGAGGAGGCTGGGTGAGAGGTGTTAAGATTAATTGTTCATGTGTTTGCATATGATAGAGTGAGAGAGAGGGCGCGAAGGAAGATGGTGGTAGGGGACCAGCAGCTCTGGGAAGGGGGGGATTTTATCAACTCAGGGTCTAGGATATCTGCTTCCAAGCAGAGCCCATGGGGTGTGGCCTAAGGAGCTTGGGGGCTCCAGGAA... |
Task1_train_46743 | This variant is located on Chromosome 19. Evaluate its biological effect and specify any disease association. | Benign | GGAACCCCAGCCCCATCCATGCCCCCATCTCTGTTGGCTCCTCAGGGCTCACTCCTGGAGGTGGTGGGCAAAGGACAATCTGTCATTCACGGATCCCTGAGGAAGGAACACACAGGGAGGCATTCAGACACCAAAAGGCTCTGCAGCCCAGGTTGGCCCTGCTTGGGATAGCAGCTCCCCCAACCATGCCTTGGCCCCAGGGCTGAGCCCCCAGCCCAGCCCTACCTTACCATGGACACCTCGTCCAGGTTCTCAAACTTGGACTCATTCCGGTGACAGAATCTCACAGCCATGACCACAGACCCGATGAGCAAAAGAGA... | GGAACCCCAGCCCCATCCATGCCCCCATCTCTGTTGGCTCCTCAGGGCTCACTCCTGGAGGTGGTGGGCAAAGGACAATCTGTCATTCACGGATCCCTGAGGAAGGAACACACAGGGAGGCATTCAGACACCAAAAGGCTCTGCAGCCCAGGTTGGCCCTGCTTGGGATAGCAGCTCCCCCAACCATGCCTTGGCCCCAGGGCTGAGCCCCCAGCCCAGCCCTACCTTACCATGGACACCTCGTCCAGGTTCTCAAACTTGGACTCATTCCGGTGACAGAATCTCACAGCCATGACCACAGACCCGATGAGCAAAAGAGA... |
Task1_train_46744 | Consider a variant on Chromosome 19. Determine its clinical classification and disease relevance. | Benign | AGTTCATGTGGAGTTGGTGCCTCTGACAGTTCATCAGTCAGGTTCATAGTGGGTGTACACAAGCTGGGTGCTCCCAGCTACTGGGGAGGCTGAGGCGGGAGGATTGCCTGACCCCAGGAATTCAAGGCTGTAGTGCGCCATGATTGCGCCACTGCACTCCTGCCTGGGAGACATAATGAGACCTTGTCTCTACAAAAAAATAAAACAAAAATTAGCCAGGCATGGTGGTGCATGCCTAGTCCCAGCTACTCAGGAGGCTGAGGTGGGAGGATCGCTTGAGTCCAGGAGTTCAAGGCTGCAGTAAGCCATGATCATGCCAC... | AGTTCATGTGGAGTTGGTGCCTCTGACAGTTCATCAGTCAGGTTCATAGTGGGTGTACACAAGCTGGGTGCTCCCAGCTACTGGGGAGGCTGAGGCGGGAGGATTGCCTGACCCCAGGAATTCAAGGCTGTAGTGCGCCATGATTGCGCCACTGCACTCCTGCCTGGGAGACATAATGAGACCTTGTCTCTACAAAAAAATAAAACAAAAATTAGCCAGGCATGGTGGTGCATGCCTAGTCCCAGCTACTCAGGAGGCTGAGGTGGGAGGATCGCTTGAGTCCAGGAGTTCAAGGCTGCAGTAAGCCATGATCATGCCAC... |
Task1_train_46745 | Given this context: Chromosome 19 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GGGTTCAAGTAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGCGCCCGCTACCAGGCCTGGCTAATTTTTGTATTTTTTAGCAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAAGTGATCCACCCGCCTCGGCCTCCCAAACTGCTAGGATTACAGGCATGAGCCACCGTGCCCAGCCCTTTTTTTTTTTTTTTTTAAGAGACGGGGTCTCACTCTGTCGCCCAGGCTGAAGCACAGTGGCACAATCACAGCTCACTGCATTCTCAAACTCTGGGATTCAAGCAACCTCCCGCCTCAGC... | GGGTTCAAGTAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGCGCCCGCTACCAGGCCTGGCTAATTTTTGTATTTTTTAGCAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAAGTGATCCACCCGCCTCGGCCTCCCAAACTGCTAGGATTACAGGCATGAGCCACCGTGCCCAGCCCTTTTTTTTTTTTTTTTTAAGAGACGGGGTCTCACTCTGTCGCCCAGGCTGAAGCACAGTGGCACAATCACAGCTCACTGCATTCTCAAACTCTGGGATTCAAGCAACCTCCCGCCTCAGC... |
Task1_train_46746 | Chromosome 19 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GTGAACACGCAAGGTCAAGCAGTTAGACACTGAGCTGTGTTGGAAACTGGGCACTTTCTCCGAGGCTGGAGTGGGCCGGTAGGGGAAGTGTAGGGTCATGTACCTATAGCCGGTTTCAGTCTCTTGCGTATCCTTAAACCTCTGGAGTGTCCCCATGGACTCCGGAGGAAAAACAGACTTCACCGCAAGGTCCCCTTCTAAACTGCTTTCCCGTGACTCATCTATCTTGTTGACGGCAGGCAGGCTGGCCACAGACATAGTGGAAAGGCTGAGGGAACTAGAACTTTGCAGAGAGCTTTCGGAATTGTTCTCCTGACTGT... | GTGAACACGCAAGGTCAAGCAGTTAGACACTGAGCTGTGTTGGAAACTGGGCACTTTCTCCGAGGCTGGAGTGGGCCGGTAGGGGAAGTGTAGGGTCATGTACCTATAGCCGGTTTCAGTCTCTTGCGTATCCTTAAACCTCTGGAGTGTCCCCATGGACTCCGGAGGAAAAACAGACTTCACCGCAAGGTCCCCTTCTAAACTGCTTTCCCGTGACTCATCTATCTTGTTGACGGCAGGCAGGCTGGCCACAGACATAGTGGAAAGGCTGAGGGAACTAGAACTTTGCAGAGAGCTTTCGGAATTGTTCTCCTGACTGT... |
Task1_train_46747 | Chromosome 19 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CTGAGTTTTGGTCACCATGGTGACCTGCAAGGGACTTGGGGCCCCCTTGTCTATCACCTCCCTAGTACCCGGGGGGGCCTGTTTGCGATTTGGGGGCTGATACCTCCTCCCCAGGCTCTCCCTGGAAGCCCTGGATGCCTGCTGCTGGCCTCTGGCCACTAAGGGTTGGTAGAGACCACGATGTACCCCTGAGGACTGACACCAAGGCAGGCCCCCACAGGTGAGGTAAGGCTGGTGAACATGGGCAGCCCTCCCACCACCCACGCTGCAAGGAAGCCTACCCGAGGCCACCCTGCCCTCCCTGGTCGATAGATAAGAGG... | CTGAGTTTTGGTCACCATGGTGACCTGCAAGGGACTTGGGGCCCCCTTGTCTATCACCTCCCTAGTACCCGGGGGGGCCTGTTTGCGATTTGGGGGCTGATACCTCCTCCCCAGGCTCTCCCTGGAAGCCCTGGATGCCTGCTGCTGGCCTCTGGCCACTAAGGGTTGGTAGAGACCACGATGTACCCCTGAGGACTGACACCAAGGCAGGCCCCCACAGGTGAGGTAAGGCTGGTGAACATGGGCAGCCCTCCCACCACCCACGCTGCAAGGAAGCCTACCCGAGGCCACCCTGCCCTCCCTGGTCGATAGATAAGAGG... |
Task1_train_46748 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CCTCCTCCCCAGGCTCTCCCTGGAAGCCCTGGATGCCTGCTGCTGGCCTCTGGCCACTAAGGGTTGGTAGAGACCACGATGTACCCCTGAGGACTGACACCAAGGCAGGCCCCCACAGGTGAGGTAAGGCTGGTGAACATGGGCAGCCCTCCCACCACCCACGCTGCAAGGAAGCCTACCCGAGGCCACCCTGCCCTCCCTGGTCGATAGATAAGAGGCCACCCTGCTGACCACATGTGGCCTGTGGCAGCTCGGGGCTGTGCCATAGATCACAGAGGGCTGGTTCATGCTTGGGCCCACACAGTTGGCAATGAGAGGCT... | CCTCCTCCCCAGGCTCTCCCTGGAAGCCCTGGATGCCTGCTGCTGGCCTCTGGCCACTAAGGGTTGGTAGAGACCACGATGTACCCCTGAGGACTGACACCAAGGCAGGCCCCCACAGGTGAGGTAAGGCTGGTGAACATGGGCAGCCCTCCCACCACCCACGCTGCAAGGAAGCCTACCCGAGGCCACCCTGCCCTCCCTGGTCGATAGATAAGAGGCCACCCTGCTGACCACATGTGGCCTGTGGCAGCTCGGGGCTGTGCCATAGATCACAGAGGGCTGGTTCATGCTTGGGCCCACACAGTTGGCAATGAGAGGCT... |
Task1_train_46749 | A mutation on Chromosome 19 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CTCTCCCTGGAAGCCCTGGATGCCTGCTGCTGGCCTCTGGCCACTAAGGGTTGGTAGAGACCACGATGTACCCCTGAGGACTGACACCAAGGCAGGCCCCCACAGGTGAGGTAAGGCTGGTGAACATGGGCAGCCCTCCCACCACCCACGCTGCAAGGAAGCCTACCCGAGGCCACCCTGCCCTCCCTGGTCGATAGATAAGAGGCCACCCTGCTGACCACATGTGGCCTGTGGCAGCTCGGGGCTGTGCCATAGATCACAGAGGGCTGGTTCATGCTTGGGCCCACACAGTTGGCAATGAGAGGCTGCCACAGACTCGG... | CTCTCCCTGGAAGCCCTGGATGCCTGCTGCTGGCCTCTGGCCACTAAGGGTTGGTAGAGACCACGATGTACCCCTGAGGACTGACACCAAGGCAGGCCCCCACAGGTGAGGTAAGGCTGGTGAACATGGGCAGCCCTCCCACCACCCACGCTGCAAGGAAGCCTACCCGAGGCCACCCTGCCCTCCCTGGTCGATAGATAAGAGGCCACCCTGCTGACCACATGTGGCCTGTGGCAGCTCGGGGCTGTGCCATAGATCACAGAGGGCTGGTTCATGCTTGGGCCCACACAGTTGGCAATGAGAGGCTGCCACAGACTCGG... |
Task1_train_46750 | Given this variant on Chromosome 19, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | ACAGAGGGCTGGTTCATGCTTGGGCCCACACAGTTGGCAATGAGAGGCTGCCACAGACTCGGGGGTGGCTGCATGTGGGACAGCTTGAGCAAACTGGGGCCCTCCCCACTCCCCTCGGGGTTAAAATCTGATGCCAATGTGCCAGGCTCCAGGGTCGGGCATGCTTCTTCCTTTTGGAACTTGGGGCTCAAATCCAGGTTTGAGGAGAAGTCCCTGCTGGACTCCATCATCTCCCGGGACAGCATGGGATACAGGCCAGTGATCAGGGGACCCTGGTGAATGCTGGTGATGACGCTACCCATCACCGAGGCTCCCACAGT... | ACAGAGGGCTGGTTCATGCTTGGGCCCACACAGTTGGCAATGAGAGGCTGCCACAGACTCGGGGGTGGCTGCATGTGGGACAGCTTGAGCAAACTGGGGCCCTCCCCACTCCCCTCGGGGTTAAAATCTGATGCCAATGTGCCAGGCTCCAGGGTCGGGCATGCTTCTTCCTTTTGGAACTTGGGGCTCAAATCCAGGTTTGAGGAGAAGTCCCTGCTGGACTCCATCATCTCCCGGGACAGCATGGGATACAGGCCAGTGATCAGGGGACCCTGGTGAATGCTGGTGATGACGCTACCCATCACCGAGGCTCCCACAGT... |
Task1_train_46751 | A mutation located on Chromosome 19 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GACTCCTCCTGCAGGCCACCTTCACCAGGGCCGGCGTCTTAGTCACCCCGCTTCCTGTTGATTTCGAGGCGGCCTTGGGGAGGATGGTTCCAGTCCTCAGGGCCACCCGACACCAAGACTGGCTCAGGAGAGCACCCAGCTCACCCTGACACAGGGCCTGGCTCAGAGCCACCCACTCCTCCTCCGTCAAAGCCTTGCTAAGCACCTCGGCCAATTTACCCTGCATGACCTTGGTGAGTTCCGCCCGCAGCTCGCCCCGGGACAGGGCTCGGGACAGGGTCAGGCGCAGCTCACTCCAGGACAGCGCCTTCACCAGCGCC... | GACTCCTCCTGCAGGCCACCTTCACCAGGGCCGGCGTCTTAGTCACCCCGCTTCCTGTTGATTTCGAGGCGGCCTTGGGGAGGATGGTTCCAGTCCTCAGGGCCACCCGACACCAAGACTGGCTCAGGAGAGCACCCAGCTCACCCTGACACAGGGCCTGGCTCAGAGCCACCCACTCCTCCTCCGTCAAAGCCTTGCTAAGCACCTCGGCCAATTTACCCTGCATGACCTTGGTGAGTTCCGCCCGCAGCTCGCCCCGGGACAGGGCTCGGGACAGGGTCAGGCGCAGCTCACTCCAGGACAGCGCCTTCACCAGCGCC... |
Task1_train_46752 | A genetic alteration is present on Chromosome 19. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GCATGACCTTGGTGAGTTCCGCCCGCAGCTCGCCCCGGGACAGGGCTCGGGACAGGGTCAGGCGCAGCTCACTCCAGGACAGCGCCTTCACCAGCGCCATGCTCAGCATGCTCTGGGGCAGGGCTTTGGTGACAGTGGCACCCAGGACCTCCTTGGACAGGGCCTGGTTCAGAGCTGCCCAGACTTCTCCCTGGGAGAGGGCTTTGGCCAACAGAGTGCGGAGATCCTCCTGGGATGCCAGCACACCAGCTACTTCAGCACACAAGGAGGCCAGCAGGGAGCCTACCGTGTCCTCCTGGCAGGGCACCGCCTGGCCGGGC... | GCATGACCTTGGTGAGTTCCGCCCGCAGCTCGCCCCGGGACAGGGCTCGGGACAGGGTCAGGCGCAGCTCACTCCAGGACAGCGCCTTCACCAGCGCCATGCTCAGCATGCTCTGGGGCAGGGCTTTGGTGACAGTGGCACCCAGGACCTCCTTGGACAGGGCCTGGTTCAGAGCTGCCCAGACTTCTCCCTGGGAGAGGGCTTTGGCCAACAGAGTGCGGAGATCCTCCTGGGATGCCAGCACACCAGCTACTTCAGCACACAAGGAGGCCAGCAGGGAGCCTACCGTGTCCTCCTGGCAGGGCACCGCCTGGCCGGGC... |
Task1_train_46753 | A mutation on Chromosome 19 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CTTGGACAGGGCCTGGTTCAGAGCTGCCCAGACTTCTCCCTGGGAGAGGGCTTTGGCCAACAGAGTGCGGAGATCCTCCTGGGATGCCAGCACACCAGCTACTTCAGCACACAAGGAGGCCAGCAGGGAGCCTACCGTGTCCTCCTGGCAGGGCACCGCCTGGCCGGGCATTGATGGCTGGGCACGTGTGGCTCCGTTGTCTCCCCAGGACTCAACGTTGCATGTGGAATGGCCGGTGGGTGCCATCGGCGGCACCAGCATACCCTGGACCTCACAGGCTGCCGGGCATGGTCCCCCCTGAGTGGTCTTCCCCGGCACGT... | CTTGGACAGGGCCTGGTTCAGAGCTGCCCAGACTTCTCCCTGGGAGAGGGCTTTGGCCAACAGAGTGCGGAGATCCTCCTGGGATGCCAGCACACCAGCTACTTCAGCACACAAGGAGGCCAGCAGGGAGCCTACCGTGTCCTCCTGGCAGGGCACCGCCTGGCCGGGCATTGATGGCTGGGCACGTGTGGCTCCGTTGTCTCCCCAGGACTCAACGTTGCATGTGGAATGGCCGGTGGGTGCCATCGGCGGCACCAGCATACCCTGGACCTCACAGGCTGCCGGGCATGGTCCCCCCTGAGTGGTCTTCCCCGGCACGT... |
Task1_train_46754 | Mutation context: Chromosome 19. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GGAGGCCAGCAGGGAGCCTACCGTGTCCTCCTGGCAGGGCACCGCCTGGCCGGGCATTGATGGCTGGGCACGTGTGGCTCCGTTGTCTCCCCAGGACTCAACGTTGCATGTGGAATGGCCGGTGGGTGCCATCGGCGGCACCAGCATACCCTGGACCTCACAGGCTGCCGGGCATGGTCCCCCCTGAGTGGTCTTCCCCGGCACGTGTCCGTGGGGCTGTGGCTGGGTCTGTCTGTCCTCTGGCTTGGCCCAGGGTGGGGCGCTGAGGCCACCGAGGCGCTGGCAGGCGTGGTTGGACACCTTGGACCCTGTTAGGAGCA... | GGAGGCCAGCAGGGAGCCTACCGTGTCCTCCTGGCAGGGCACCGCCTGGCCGGGCATTGATGGCTGGGCACGTGTGGCTCCGTTGTCTCCCCAGGACTCAACGTTGCATGTGGAATGGCCGGTGGGTGCCATCGGCGGCACCAGCATACCCTGGACCTCACAGGCTGCCGGGCATGGTCCCCCCTGAGTGGTCTTCCCCGGCACGTGTCCGTGGGGCTGTGGCTGGGTCTGTCTGTCCTCTGGCTTGGCCCAGGGTGGGGCGCTGAGGCCACCGAGGCGCTGGCAGGCGTGGTTGGACACCTTGGACCCTGTTAGGAGCA... |
Task1_train_46755 | Chromosome 19 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CGGCACCTGTGGCCAGATGTGTCTGGGAATGCATCTTGCTCAGACAGGTGTCCAGATGGGCCAGGGATGGGGTCTTGGTCAGCTCAGTGGGCAGATGTCCCTGAGATGAGGCCTTGGTCAGCGGGGCGGCCAGTGGTCTCTGGGACAGGCAGGGTGGATGTCTCTGGGATGAGGCATTGGTCAGTGGGGCAGCCAGCTGTCCCCGGGGCAGGGTGACAGCCATGTCTACAGGCACATACACGTGAGGTGGCTTGTCCCCTTCCTCAGCAACTTTTGTCCAGGATGGAGCCCCAGCCATTTCCACTGCCACACTGGTCTTA... | CGGCACCTGTGGCCAGATGTGTCTGGGAATGCATCTTGCTCAGACAGGTGTCCAGATGGGCCAGGGATGGGGTCTTGGTCAGCTCAGTGGGCAGATGTCCCTGAGATGAGGCCTTGGTCAGCGGGGCGGCCAGTGGTCTCTGGGACAGGCAGGGTGGATGTCTCTGGGATGAGGCATTGGTCAGTGGGGCAGCCAGCTGTCCCCGGGGCAGGGTGACAGCCATGTCTACAGGCACATACACGTGAGGTGGCTTGTCCCCTTCCTCAGCAACTTTTGTCCAGGATGGAGCCCCAGCCATTTCCACTGCCACACTGGTCTTA... |
Task1_train_46756 | This alteration occurs on Chromosome 19. Is it associated with a disease or is it a benign variant? | Benign | TCACGCCTCTAATCCCAGTACTTTGGGAGGCCGAGGCCAGCGGATCACAAGGTCAGGAGATTGAGACCATCCTAGCTAACACGGTGAAACCCCATCTCTACTAAAAATACAAAAAAAAATTAGCCAGGCGTGGTGGGGGGTGCTCATAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATAGCATGAACCTGGGAGCTGGAGCTTGCAGGTTGGAGTGCAATGGCATGATCTCAGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGGCTCCCGAGCAGCTGGGATTACAGGCATGTGCCAC... | TCACGCCTCTAATCCCAGTACTTTGGGAGGCCGAGGCCAGCGGATCACAAGGTCAGGAGATTGAGACCATCCTAGCTAACACGGTGAAACCCCATCTCTACTAAAAATACAAAAAAAAATTAGCCAGGCGTGGTGGGGGGTGCTCATAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATAGCATGAACCTGGGAGCTGGAGCTTGCAGGTTGGAGTGCAATGGCATGATCTCAGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGGCTCCCGAGCAGCTGGGATTACAGGCATGTGCCAC... |
Task1_train_46757 | This variant is located on Chromosome 19. Evaluate its biological effect and specify any disease association. | Benign | AATTAGCCAGGCGTGGTGGGGGGTGCTCATAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATAGCATGAACCTGGGAGCTGGAGCTTGCAGGTTGGAGTGCAATGGCATGATCTCAGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGGCTCCCGAGCAGCTGGGATTACAGGCATGTGCCACCACGACCGGTTAATTTCTGAAATTTTTTAGTAGAGACAGGGTTTCATCATGTTGGTCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCGCCCGCCTTGGCCTCCCAAAGTGCTG... | AATTAGCCAGGCGTGGTGGGGGGTGCTCATAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATAGCATGAACCTGGGAGCTGGAGCTTGCAGGTTGGAGTGCAATGGCATGATCTCAGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGGCTCCCGAGCAGCTGGGATTACAGGCATGTGCCACCACGACCGGTTAATTTCTGAAATTTTTTAGTAGAGACAGGGTTTCATCATGTTGGTCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCGCCCGCCTTGGCCTCCCAAAGTGCTG... |
Task1_train_46758 | With a mutation on Chromosome 19, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CTCAGTTGCCCCATCTGTGCCCTGGGTAGGAATATCCTGGATCCCCTTGGGTCTGATGGGGTAGCCGATGCCTGATTTGCACCCACAACGTGGGAGGTTATAACCTGTCCCCAAGTTGCAAATGGGGAAACTGAGGTACAGGGATGCCAGGGACCCTCCTGAATGTGCACAGCACCTGGGAAACCCGGGGACGGGGTCGGGCGTGCGGTGTGGGCATGGTCCCTGACCTGGGCTGGGGCCAGGATCCAAGAGAAACAATGGGGGTGTGGTGCATGGATAGAAGTTTGTGATGGGCAGAGCCAGCTGGAGCTGGTTCTGAA... | CTCAGTTGCCCCATCTGTGCCCTGGGTAGGAATATCCTGGATCCCCTTGGGTCTGATGGGGTAGCCGATGCCTGATTTGCACCCACAACGTGGGAGGTTATAACCTGTCCCCAAGTTGCAAATGGGGAAACTGAGGTACAGGGATGCCAGGGACCCTCCTGAATGTGCACAGCACCTGGGAAACCCGGGGACGGGGTCGGGCGTGCGGTGTGGGCATGGTCCCTGACCTGGGCTGGGGCCAGGATCCAAGAGAAACAATGGGGGTGTGGTGCATGGATAGAAGTTTGTGATGGGCAGAGCCAGCTGGAGCTGGTTCTGAA... |
Task1_train_46759 | A variant has been detected on Chromosome 19. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | GTGAAGAATATTTTCATGCACACCACATCTCCCAGGTTATATATACTTCCTGTTTAGGATGTTGGAATTTTGAGGTGTGCTGAGTCCAGCCCCCTCTCCACACCAAACTGCCTGCCCATCCTGAATCTCTGAGAGGAATGGCGATGGGTGTCTTGAGGGACAGAGTACCCACTTCCAGCAGTGAGGTGTATCTGCTGGGAATGCCATCACCCACAGGCCAACCTGAATGACTGCAGGTTCCCCTTAACGTATTCAGTGAGTGCCCACTTTATGCCAGGCCCCGGACACAGCTGTAAAAAGACACACAAGGACCACCCCAC... | GTGAAGAATATTTTCATGCACACCACATCTCCCAGGTTATATATACTTCCTGTTTAGGATGTTGGAATTTTGAGGTGTGCTGAGTCCAGCCCCCTCTCCACACCAAACTGCCTGCCCATCCTGAATCTCTGAGAGGAATGGCGATGGGTGTCTTGAGGGACAGAGTACCCACTTCCAGCAGTGAGGTGTATCTGCTGGGAATGCCATCACCCACAGGCCAACCTGAATGACTGCAGGTTCCCCTTAACGTATTCAGTGAGTGCCCACTTTATGCCAGGCCCCGGACACAGCTGTAAAAAGACACACAAGGACCACCCCAC... |
Task1_train_46760 | This variant is present on Chromosome 19. Is the change likely to result in a pathogenic outcome? | Benign | GGGCTCCCACCCTCATCCCAGGAATCCCCTGACTCAGCCTCCTCCCCAGAGACACAACCCAAAAGCACAGCAGGTGACACCACCTGGGCTGCCCTGGGCCAGCTGGCGCCGAGAGCGAAGTGGCCATCTGCAACTGGCCGCCATCGCCACATGGGACCACTGCAGCCCCTGTCGCACATGGTGGTGGAACAGCCGCTGCACGCTGGCCACTGCTTCTGCTGGTTCCTATAAATGAACAGCTGCGCAGGCTCATGGCCACGGTGCTAGGCGGGTGCTACTGCTGCTCAGTTTAGGTGCCTGGGCTGTGGTCTCGGAGCCGC... | GGGCTCCCACCCTCATCCCAGGAATCCCCTGACTCAGCCTCCTCCCCAGAGACACAACCCAAAAGCACAGCAGGTGACACCACCTGGGCTGCCCTGGGCCAGCTGGCGCCGAGAGCGAAGTGGCCATCTGCAACTGGCCGCCATCGCCACATGGGACCACTGCAGCCCCTGTCGCACATGGTGGTGGAACAGCCGCTGCACGCTGGCCACTGCTTCTGCTGGTTCCTATAAATGAACAGCTGCGCAGGCTCATGGCCACGGTGCTAGGCGGGTGCTACTGCTGCTCAGTTTAGGTGCCTGGGCTGTGGTCTCGGAGCCGC... |
Task1_train_46761 | A mutation located on Chromosome 19 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CGACGGTATTCAGGACGGTCACCCTGTACAGGTTTGTAGCCTGGGAACAAGGGCCCTACCGTCTGGCCGAGGTGTGCAGAGGCTCTGCCATCCAGGTTTGTGTAAGTTGCCCTGTGATCCTCATGCACAGCCATGAAATCGCCGGACAACGCGTTTTTTCAGAAGTCACCCCCATTGTTAAGTGATGCTTGACTGTACTTAGAATCAACATTGAAAAACCAGGGGAATGCCCGTAGAACACCAGATTTCTGGCTGCTCTTGAAGAATCAGACAGCCCAGTGGCCATGGCCGATGTCTTGCACCTCGAGACGGGCCACAGT... | CGACGGTATTCAGGACGGTCACCCTGTACAGGTTTGTAGCCTGGGAACAAGGGCCCTACCGTCTGGCCGAGGTGTGCAGAGGCTCTGCCATCCAGGTTTGTGTAAGTTGCCCTGTGATCCTCATGCACAGCCATGAAATCGCCGGACAACGCGTTTTTTCAGAAGTCACCCCCATTGTTAAGTGATGCTTGACTGTACTTAGAATCAACATTGAAAAACCAGGGGAATGCCCGTAGAACACCAGATTTCTGGCTGCTCTTGAAGAATCAGACAGCCCAGTGGCCATGGCCGATGTCTTGCACCTCGAGACGGGCCACAGT... |
Task1_train_46762 | This variant is located on Chromosome 19. Evaluate its biological effect and specify any disease association. | Benign | GGCCCTACCGTCTGGCCGAGGTGTGCAGAGGCTCTGCCATCCAGGTTTGTGTAAGTTGCCCTGTGATCCTCATGCACAGCCATGAAATCGCCGGACAACGCGTTTTTTCAGAAGTCACCCCCATTGTTAAGTGATGCTTGACTGTACTTAGAATCAACATTGAAAAACCAGGGGAATGCCCGTAGAACACCAGATTTCTGGCTGCTCTTGAAGAATCAGACAGCCCAGTGGCCATGGCCGATGTCTTGCACCTCGAGACGGGCCACAGTGCTCTGGTTTGCCTCAGGCCCCACCCGCCCCTGTCGTCCCACATCCATACC... | GGCCCTACCGTCTGGCCGAGGTGTGCAGAGGCTCTGCCATCCAGGTTTGTGTAAGTTGCCCTGTGATCCTCATGCACAGCCATGAAATCGCCGGACAACGCGTTTTTTCAGAAGTCACCCCCATTGTTAAGTGATGCTTGACTGTACTTAGAATCAACATTGAAAAACCAGGGGAATGCCCGTAGAACACCAGATTTCTGGCTGCTCTTGAAGAATCAGACAGCCCAGTGGCCATGGCCGATGTCTTGCACCTCGAGACGGGCCACAGTGCTCTGGTTTGCCTCAGGCCCCACCCGCCCCTGTCGTCCCACATCCATACC... |
Task1_train_46763 | Mutation context: Chromosome 19. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CTCTGGTGCCTCCCTTAGGTGGGCCTTGAGCTGGTTTTTAACCAAACATCCTTCCAAACTCGGGCTGCGACCTGCTTCCTGAGTTTTCTGTATTTCCAAGGAGCCCTCCGACCAGGGAGAGGCTGGTGGAGTAAGGTCCAGCGGTATTCGGGGGTCCTCTGTCACCTCGCCCTGAAAACAGCAGCTCCCATCACCTTCACTGGGTCCCGATGGAGCCGTCTCAGAGGCCGAGGGGCCCTCTGTGTGGGGGTGGGACGCAGGGGCTCTCAGAGCAAGGGCCACAAAGCCGATGGCACAGATGTGCCCCTGGGCCTGGCCCG... | CTCTGGTGCCTCCCTTAGGTGGGCCTTGAGCTGGTTTTTAACCAAACATCCTTCCAAACTCGGGCTGCGACCTGCTTCCTGAGTTTTCTGTATTTCCAAGGAGCCCTCCGACCAGGGAGAGGCTGGTGGAGTAAGGTCCAGCGGTATTCGGGGGTCCTCTGTCACCTCGCCCTGAAAACAGCAGCTCCCATCACCTTCACTGGGTCCCGATGGAGCCGTCTCAGAGGCCGAGGGGCCCTCTGTGTGGGGGTGGGACGCAGGGGCTCTCAGAGCAAGGGCCACAAAGCCGATGGCACAGATGTGCCCCTGGGCCTGGCCCG... |
Task1_train_46764 | Given this context: Chromosome 19 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GAAGCTGCTCGTTCTCCGCTGGACTCAGAAGCCAAGCTGCTTCCCGCCTAGACTCGGCGCAGGGCCCCGCACCGGTGAGGAAGGTGCTTTTGGCCCCATTGCGAGGGGCCTTGGCCAGGACTGGCCCTGTGGCCAGGAGGCGAGAAGGTGGCTGTTCCCGGATTGACGGCTTTTTCCCGGGGGCCTTTGGAAGATTTGGTGGAAGGACAAGAGGGCCTGTCCCTGTCCCCGTCCCCAGGAGGTACCGACAGTCCCTGTGCTGGTTAGACACGGAGCGCTGCACACCGAAAGCCCAAATTGGGAGCTCTGCCTGCCGGCAA... | GAAGCTGCTCGTTCTCCGCTGGACTCAGAAGCCAAGCTGCTTCCCGCCTAGACTCGGCGCAGGGCCCCGCACCGGTGAGGAAGGTGCTTTTGGCCCCATTGCGAGGGGCCTTGGCCAGGACTGGCCCTGTGGCCAGGAGGCGAGAAGGTGGCTGTTCCCGGATTGACGGCTTTTTCCCGGGGGCCTTTGGAAGATTTGGTGGAAGGACAAGAGGGCCTGTCCCTGTCCCCGTCCCCAGGAGGTACCGACAGTCCCTGTGCTGGTTAGACACGGAGCGCTGCACACCGAAAGCCCAAATTGGGAGCTCTGCCTGCCGGCAA... |
Task1_train_46765 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GCCACCCTGCCCGTCTGACCACGTGCAGGCCCTGGGAAGGTGGGACTGGGGCCAGCTATGGCCCCCCAGGGTGGCCACCACAAGGTAGAGCTCAGGAGAGACTCACTCCATGGAGGATGGAACGCAGGGAAGGGCAACGGAACTACAGTGTGAACAACTCTGAGGCAAGGGCTTTGGAAACGGCAGCAGGGGAGTCCTGGACCCCCAGCCATGGCCTCCGACCTGGTGATGCCACGTGCAGGCCCCGCCAGCCCCACGGCACAGTTACAAGCTGGTCAAGTAACATGTTGCTCCAGGCACAACCTCCACTCTCCCTCCAT... | GCCACCCTGCCCGTCTGACCACGTGCAGGCCCTGGGAAGGTGGGACTGGGGCCAGCTATGGCCCCCCAGGGTGGCCACCACAAGGTAGAGCTCAGGAGAGACTCACTCCATGGAGGATGGAACGCAGGGAAGGGCAACGGAACTACAGTGTGAACAACTCTGAGGCAAGGGCTTTGGAAACGGCAGCAGGGGAGTCCTGGACCCCCAGCCATGGCCTCCGACCTGGTGATGCCACGTGCAGGCCCCGCCAGCCCCACGGCACAGTTACAAGCTGGTCAAGTAACATGTTGCTCCAGGCACAACCTCCACTCTCCCTCCAT... |
Task1_train_46766 | Consider this mutation on Chromosome 19. Is this a benign change or a disease-causing variant? | Benign | GATAGGGTCTCACTTTTGACATAGTAAGAGCACCAACATCTCAGACAAACACTGCCACTTTAAGTTCCAGCCCCCTTTCTAGCCTCATGAATTTTAAGGAAATTTCTTTTTTCTTTTTTTTTAATAGAGAAGTCTCGCTCTTGTTCCCCAGGCTTGAATGCAATGGCTGGATCTTGGCTCACTGCAACCTCCACCTCCTGGGTTCAAACGATTCTCCTGCCTCTGCCTCCCAAGTAGCTGGGATTAAGGTGCCTGCCACCATGCCCGGCTAATTTTTGTATTTTTTAGTAGAGACGGGGTTTCACCAAGTTGGTCAGGCT... | GATAGGGTCTCACTTTTGACATAGTAAGAGCACCAACATCTCAGACAAACACTGCCACTTTAAGTTCCAGCCCCCTTTCTAGCCTCATGAATTTTAAGGAAATTTCTTTTTTCTTTTTTTTTAATAGAGAAGTCTCGCTCTTGTTCCCCAGGCTTGAATGCAATGGCTGGATCTTGGCTCACTGCAACCTCCACCTCCTGGGTTCAAACGATTCTCCTGCCTCTGCCTCCCAAGTAGCTGGGATTAAGGTGCCTGCCACCATGCCCGGCTAATTTTTGTATTTTTTAGTAGAGACGGGGTTTCACCAAGTTGGTCAGGCT... |
Task1_train_46767 | This variant lies on Chromosome 19. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AGCTCAGGAGTTCGAGACCAGTCTGGGCAACATGATTCTCTACAAAAAAATACAAAAAAAGTTAGCCAGGCATGGTGGTACATGCCTATAGTCCCAGCTACTCAGGAGGCTGAGGCGGAAGGATCACTTGAGCCTAGGAGGTCGGGGCTGCAGTGAGCCATGGTCATGCCACTGCACTCCAGCCTGGGTGACAGAGCACGACCCTGTCTCAAAAAAACAAAAACAAGGAAAGAAAGTCAACCCTTCTTTTTTTCAAAGGTTAAAAAGAAAAAAAAAGGAACAAGCGTTCTTAACCTTGGCTGCAGAAAGGTACGAATCCC... | AGCTCAGGAGTTCGAGACCAGTCTGGGCAACATGATTCTCTACAAAAAAATACAAAAAAAGTTAGCCAGGCATGGTGGTACATGCCTATAGTCCCAGCTACTCAGGAGGCTGAGGCGGAAGGATCACTTGAGCCTAGGAGGTCGGGGCTGCAGTGAGCCATGGTCATGCCACTGCACTCCAGCCTGGGTGACAGAGCACGACCCTGTCTCAAAAAAACAAAAACAAGGAAAGAAAGTCAACCCTTCTTTTTTTCAAAGGTTAAAAAGAAAAAAAAAGGAACAAGCGTTCTTAACCTTGGCTGCAGAAAGGTACGAATCCC... |
Task1_train_46768 | This is a variant located on Chromosome 19. Is this mutation a likely cause of disease or not? | Benign | AACTACACACACACACAAAAATTAAAATATTTATCTTCCCTCTGAGCCACACACAAAGACCTCAACCACCCCCTTCTATCTTTCCTATTTTTATTTATTTATTTATTTTGAGACAGAGTCTCGCTCTGTCACCCACGCTGGAGTGCAATGGCGCGATCTTGGCTCACTGCAACCTCTGCCTCTGGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTGGCTGGGATTACAGGCACCTGCCACCGCACCTGGCTGATTTTTGTATTTTTAGTAGGGATGGGGTTTCACCATGTTGGCCAGGGTGGTCTCAAACTCTTG... | AACTACACACACACACAAAAATTAAAATATTTATCTTCCCTCTGAGCCACACACAAAGACCTCAACCACCCCCTTCTATCTTTCCTATTTTTATTTATTTATTTATTTTGAGACAGAGTCTCGCTCTGTCACCCACGCTGGAGTGCAATGGCGCGATCTTGGCTCACTGCAACCTCTGCCTCTGGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTGGCTGGGATTACAGGCACCTGCCACCGCACCTGGCTGATTTTTGTATTTTTAGTAGGGATGGGGTTTCACCATGTTGGCCAGGGTGGTCTCAAACTCTTG... |
Task1_train_46769 | Chromosome 19 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GGCCCTGAGGAAGGATCTGGATGGCCTCAGACCCCACCCAGGCTCTCTGCAAAGTGCTCCTCTATTTCCCTTGGGGATCCTTGCCCCCAACCCCCGAACACATACACCAAACCTACTAACCTTTCTCTGAAAGTGGCATGCGACCCTGGCCTAGCCAGTCGGAGCATTCCAGCCCCCTGTCCATGATGCTCAGTAAGGGATGGGCAAGTGATTCACGCTGGGCCAATCTGAGCCTGCCTAAGACTTGTGCTTAAGCTCGGGGGTAATAAGGGCTCACATTGCTCTGGGGTGGCTGAGTGGGGTGCATGGAAGCCTGAAGC... | GGCCCTGAGGAAGGATCTGGATGGCCTCAGACCCCACCCAGGCTCTCTGCAAAGTGCTCCTCTATTTCCCTTGGGGATCCTTGCCCCCAACCCCCGAACACATACACCAAACCTACTAACCTTTCTCTGAAAGTGGCATGCGACCCTGGCCTAGCCAGTCGGAGCATTCCAGCCCCCTGTCCATGATGCTCAGTAAGGGATGGGCAAGTGATTCACGCTGGGCCAATCTGAGCCTGCCTAAGACTTGTGCTTAAGCTCGGGGGTAATAAGGGCTCACATTGCTCTGGGGTGGCTGAGTGGGGTGCATGGAAGCCTGAAGC... |
Task1_train_46770 | A mutation has occurred on Chromosome 19. What is the medical relevance of this mutation? | Benign | ATTCTAGTGTAAATTCTCATATTTACGTAAAATCAATTTTGAATTAAATATTTTTTTCATATTTACATCTGCAAAAATATACTTTAGTATAAACTCTCTGATGTTTTCTAAGCTATAGATTTTGAAAAAAAAAGTCTTTCCAAATTCATTATATTTGCAGGACTCTTCTCCAATATAAATTCCATGTTGTTGAATAAAGCTGGAGCAACTGCTTCAGGTTTTCCTCTAGTACACAATGTGTGCAACAAGATCTGTGATACAAGTAAAGGTACTACAACCCCCCCTTATATTTGTAATAGCTGATTTCAGAATAAATATTC... | ATTCTAGTGTAAATTCTCATATTTACGTAAAATCAATTTTGAATTAAATATTTTTTTCATATTTACATCTGCAAAAATATACTTTAGTATAAACTCTCTGATGTTTTCTAAGCTATAGATTTTGAAAAAAAAAGTCTTTCCAAATTCATTATATTTGCAGGACTCTTCTCCAATATAAATTCCATGTTGTTGAATAAAGCTGGAGCAACTGCTTCAGGTTTTCCTCTAGTACACAATGTGTGCAACAAGATCTGTGATACAAGTAAAGGTACTACAACCCCCCCTTATATTTGTAATAGCTGATTTCAGAATAAATATTC... |
Task1_train_46771 | This variant is found on Chromosome 19. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TTTTCCAGGGACCATTGCAATTTAGAGACGTGGCCATAGAATTCTCTCTGGAGGAGTGGCATTGCCTGGACACTGCACAGTGGAATTTATATAGGGATGTGATGTTAGAGAACTACAGACACCTGGTCTTCCTTGGTGAGGATAACTTGAATGTATAATTCATAATGTACCCTAAAGGTTTTATTTCTCCTTTTTGTGAAATGTTTTTTAGTAATTTATTTTTTGCGTAAAAGAGTTTCAGATGCCCTTTTTCCAGAAAATTTTTAGAATTTGTTCATTTAGAAAAGAATTTCAAGATGTTTAATCTTTTTTTTTTTTGA... | TTTTCCAGGGACCATTGCAATTTAGAGACGTGGCCATAGAATTCTCTCTGGAGGAGTGGCATTGCCTGGACACTGCACAGTGGAATTTATATAGGGATGTGATGTTAGAGAACTACAGACACCTGGTCTTCCTTGGTGAGGATAACTTGAATGTATAATTCATAATGTACCCTAAAGGTTTTATTTCTCCTTTTTGTGAAATGTTTTTTAGTAATTTATTTTTTGCGTAAAAGAGTTTCAGATGCCCTTTTTCCAGAAAATTTTTAGAATTTGTTCATTTAGAAAAGAATTTCAAGATGTTTAATCTTTTTTTTTTTTGA... |
Task1_train_46772 | A variant on Chromosome 19 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | AGATAACATCTTCTACATACTCACTTAAGATTCAGAAATATATGGCTTTTGATTATATGCCTGTGTAATTTTCATAATAATCATCTTAATGACTCTATAATTAGAAGAAAAATAATAAAAATGTAACCTATGGAAACAATATTCTCCAACGTATTTGAAGTTTAAAGTCACTAAGGATAAGAATCACTAGAGATGCCATTCCACTATATTACTGAATAGTATGTTGTTACCGTCTGTTACCTAGAGACTTGAGTAAGGTAAAATAGGTTAATGTTGGTGGCAGGATAACACCTAATTCAATGCACAACTGTCTTAACACA... | AGATAACATCTTCTACATACTCACTTAAGATTCAGAAATATATGGCTTTTGATTATATGCCTGTGTAATTTTCATAATAATCATCTTAATGACTCTATAATTAGAAGAAAAATAATAAAAATGTAACCTATGGAAACAATATTCTCCAACGTATTTGAAGTTTAAAGTCACTAAGGATAAGAATCACTAGAGATGCCATTCCACTATATTACTGAATAGTATGTTGTTACCGTCTGTTACCTAGAGACTTGAGTAAGGTAAAATAGGTTAATGTTGGTGGCAGGATAACACCTAATTCAATGCACAACTGTCTTAACACA... |
Task1_train_46773 | Consider a variant on Chromosome 19. Determine its clinical classification and disease relevance. | Benign | TCAATGCAAAAAGTGTACTTTGAATATAATTGTTTAAGTCTCAAAATATTAATCTCCTATTTCTGTTTAGGCTAACTAAATTATGTTAACCTTGAATTACTCTTTATAATCAATGCCCTGATTTAGAATAACATTGAAAGTGTTAGCGTCTTAGTGGTTTCTACTGTGAATCTTCTGATGTTCATTTAGACTTAATTTTTTATTAATTTTTTATATTTACTGCATCTGTTAAATGCTTTCATATAAACTAGCGTTCTTTCTTTTTTTTTGAGACAGAGTCTCTGTCGCCCAGGTTGGAGTTCAGTGGCGCGATCTCGGCT... | TCAATGCAAAAAGTGTACTTTGAATATAATTGTTTAAGTCTCAAAATATTAATCTCCTATTTCTGTTTAGGCTAACTAAATTATGTTAACCTTGAATTACTCTTTATAATCAATGCCCTGATTTAGAATAACATTGAAAGTGTTAGCGTCTTAGTGGTTTCTACTGTGAATCTTCTGATGTTCATTTAGACTTAATTTTTTATTAATTTTTTATATTTACTGCATCTGTTAAATGCTTTCATATAAACTAGCGTTCTTTCTTTTTTTTTGAGACAGAGTCTCTGTCGCCCAGGTTGGAGTTCAGTGGCGCGATCTCGGCT... |
Task1_train_46774 | The following genetic variant occurs on Chromosome 19. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CATCATGGCTATAGTTAATCATAATGCTCTATATCAGGGGTATCCAATCTTTTGGCTTCCCTGGGCCACAGTGGAAGAATTGTCTTGGGCCACGCATAAAATACACTAACACTAATGGTAACTGATTAGCTTTTAAAAAAATCTCATGTTTAAAGAAAGTTTACAAATTTGTGTTTGGCCACATTCAAAGCCATCCTGGACTGCATGCAGCCAGCAGGACATGAGTTGGACAAACGTGCTCCATATGCTTAAATTTTAGTAAGACAGCAGACCTTTCACTGCAAAAGAAAACTCTGCATGGTGGCTTAATTCCAGCACTT... | CATCATGGCTATAGTTAATCATAATGCTCTATATCAGGGGTATCCAATCTTTTGGCTTCCCTGGGCCACAGTGGAAGAATTGTCTTGGGCCACGCATAAAATACACTAACACTAATGGTAACTGATTAGCTTTTAAAAAAATCTCATGTTTAAAGAAAGTTTACAAATTTGTGTTTGGCCACATTCAAAGCCATCCTGGACTGCATGCAGCCAGCAGGACATGAGTTGGACAAACGTGCTCCATATGCTTAAATTTTAGTAAGACAGCAGACCTTTCACTGCAAAAGAAAACTCTGCATGGTGGCTTAATTCCAGCACTT... |
Task1_train_46775 | Chromosome 19 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CTGTATTTATTTTATCTGAGATGGAGTCATTTTCTGTCAAGCTGGAAGCAGTGGTGCAATCTCGGCTGACTGCAACCTCTGCCTCCTAGGTTCAAGCGATTCTCCTGCTTCAGTCTCCTGAGTAGCTGGGTACAGGTGCTTTCCACTATGACTGGCTAAGTTTTTGTATTTTTAGTACAGACAGGGTTTCACCATGTTGGCTATGCTGACCTTGAACTCCTGACCTCAAATGATTCACACACCTCAGGCTCCTAAATTGCTGGTATTACAGGCGTGAACCACTGTGCCCAGCATATTTTATTTTATTTTTGAGACAGTCT... | CTGTATTTATTTTATCTGAGATGGAGTCATTTTCTGTCAAGCTGGAAGCAGTGGTGCAATCTCGGCTGACTGCAACCTCTGCCTCCTAGGTTCAAGCGATTCTCCTGCTTCAGTCTCCTGAGTAGCTGGGTACAGGTGCTTTCCACTATGACTGGCTAAGTTTTTGTATTTTTAGTACAGACAGGGTTTCACCATGTTGGCTATGCTGACCTTGAACTCCTGACCTCAAATGATTCACACACCTCAGGCTCCTAAATTGCTGGTATTACAGGCGTGAACCACTGTGCCCAGCATATTTTATTTTATTTTTGAGACAGTCT... |
Task1_train_46776 | The following genetic variant occurs on Chromosome 19. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GGCTTATGCCACCATGCCCAGTTAATTTTTGAGTTTTTAGTAGATACAGGGTTTCACCATGTTCTCTAGGCTGGTCTCATACTCCTGACCTCATGTGATTTTCCCACCTTAACCTCTCTGTGTTGAAATTACAGGAATGACCACCAACCCTGGCCTGTTCAATTTATTTGGAATTTTAAAAATTACTTTATATGCTTTTTATAGTTGCTTTTGAAATGTTTTTCATTGGGCCATGTTTCTCTAATATTTTGTGTACATTGCAATCTTTGATTGAGATTTGGACATTGACAAAAAGCTACCTGTTACAATCTTTTTATAAT... | GGCTTATGCCACCATGCCCAGTTAATTTTTGAGTTTTTAGTAGATACAGGGTTTCACCATGTTCTCTAGGCTGGTCTCATACTCCTGACCTCATGTGATTTTCCCACCTTAACCTCTCTGTGTTGAAATTACAGGAATGACCACCAACCCTGGCCTGTTCAATTTATTTGGAATTTTAAAAATTACTTTATATGCTTTTTATAGTTGCTTTTGAAATGTTTTTCATTGGGCCATGTTTCTCTAATATTTTGTGTACATTGCAATCTTTGATTGAGATTTGGACATTGACAAAAAGCTACCTGTTACAATCTTTTTATAAT... |
Task1_train_46777 | A mutation on Chromosome 19 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | AATATAGCTTTGTCCTGGCATAGTCTGAAATCAATAGTCTTGGCTAGAGATTCTGGGAATTTCTCAAACATGTTCTTAGGATGTGTCTTGTCTAAATTTTGTGTTTATTGTTTAGTTAAATGGCTTATTTTTTTTAATAATCAGTAATCACTTGCTGCAGCCATTCCCTGTTTGGGGTACTGCAGTTTCTCTGCTTCTCTAACATTTATCTTTAGACTCAGTAGACTCAAACTGTCATTCCAATGTATATCACCACTTCTTTAAGCGTTTTATGTCATGGGAGACATTAACCAGTGTCTAAGAAGCACATAGAAGCCAGA... | AATATAGCTTTGTCCTGGCATAGTCTGAAATCAATAGTCTTGGCTAGAGATTCTGGGAATTTCTCAAACATGTTCTTAGGATGTGTCTTGTCTAAATTTTGTGTTTATTGTTTAGTTAAATGGCTTATTTTTTTTAATAATCAGTAATCACTTGCTGCAGCCATTCCCTGTTTGGGGTACTGCAGTTTCTCTGCTTCTCTAACATTTATCTTTAGACTCAGTAGACTCAAACTGTCATTCCAATGTATATCACCACTTCTTTAAGCGTTTTATGTCATGGGAGACATTAACCAGTGTCTAAGAAGCACATAGAAGCCAGA... |
Task1_train_46778 | This is a variant located on Chromosome 19. Is this mutation a likely cause of disease or not? | Benign | AGGAATGAGCCACCAACAGTGGGATGTTCAATTCATTTGGAATTTTAAAAATTACTTTGTATACTTTTTATGGTTGCTTTTGAAAAGTTTATAATTTTTTTGATGGGGCCATGTTCTAATATTTGGTATACATTATCATCTTTGATAGAGATTTGGAAATTAACAAAAAGCTACCTGTTACAATCTTTATAATATAGCTTTGTCCTGGCGTAGCATGAAATCAATTGTCTTGGCTAGAGATTCTGGGAATTTTTCAAACATGTTTTTAGGATGAGTCTTGTCTAAAATTTTGTGTTTATTGTTTAGTTAAATCAGCTTAT... | AGGAATGAGCCACCAACAGTGGGATGTTCAATTCATTTGGAATTTTAAAAATTACTTTGTATACTTTTTATGGTTGCTTTTGAAAAGTTTATAATTTTTTTGATGGGGCCATGTTCTAATATTTGGTATACATTATCATCTTTGATAGAGATTTGGAAATTAACAAAAAGCTACCTGTTACAATCTTTATAATATAGCTTTGTCCTGGCGTAGCATGAAATCAATTGTCTTGGCTAGAGATTCTGGGAATTTTTCAAACATGTTTTTAGGATGAGTCTTGTCTAAAATTTTGTGTTTATTGTTTAGTTAAATCAGCTTAT... |
Task1_train_46779 | A variant found on Chromosome 19 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | TACTTTTAATTATTTCTTTGTGTCACTATAATAAAGTATTGCTCTGAACATTTACGTTATACATTACTTAATAGAATTTTACTACAAACAGCTTCTCCACTTGTATTTTCATTATGCGTCTTACATTTTAATGTTCTTACTATTTTATAGAAAAAGTCATAATGTCCAAATAATGTAAAAAAATCGAATATCTCTGATGCAGAAGCCACTGATCACATGCTTTCTCACATGTGAATAGAAATAAAATAACAGCATAATTTGAAAGCTGTATTACATCATTATTCAGCTTTCAAAAAATTTTATTCAAGGAAACAAGTATA... | TACTTTTAATTATTTCTTTGTGTCACTATAATAAAGTATTGCTCTGAACATTTACGTTATACATTACTTAATAGAATTTTACTACAAACAGCTTCTCCACTTGTATTTTCATTATGCGTCTTACATTTTAATGTTCTTACTATTTTATAGAAAAAGTCATAATGTCCAAATAATGTAAAAAAATCGAATATCTCTGATGCAGAAGCCACTGATCACATGCTTTCTCACATGTGAATAGAAATAAAATAACAGCATAATTTGAAAGCTGTATTACATCATTATTCAGCTTTCAAAAAATTTTATTCAAGGAAACAAGTATA... |
Task1_train_46780 | A mutation found on Chromosome 19 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TGTCTGAAGTGTCGGGGCCTTAGTTATTCTACTGTAAACTCTCTTGATATTTATATACAATCTATTTTGAATTAAATATTTTTTAATATTTACTGCATCTGCAAAATTATATTTTAGCATAAACTCTCTGTTGTTTTCTAAGCTGTAGTTTCTGGGGAAAAAAAAGTGTTTCTAAACTTAATACATTTGTAGGACTCATCTCCAATATAAATTCCCTGATGTTGAACAAACTTGAGCAACTGCTTTAGGATTTTCCTCCAGTACAAAATGTGTGCAATAAGATCTGTGATACTAGTAAATGTACTATGTAACTCCCTTTA... | TGTCTGAAGTGTCGGGGCCTTAGTTATTCTACTGTAAACTCTCTTGATATTTATATACAATCTATTTTGAATTAAATATTTTTTAATATTTACTGCATCTGCAAAATTATATTTTAGCATAAACTCTCTGTTGTTTTCTAAGCTGTAGTTTCTGGGGAAAAAAAAGTGTTTCTAAACTTAATACATTTGTAGGACTCATCTCCAATATAAATTCCCTGATGTTGAACAAACTTGAGCAACTGCTTTAGGATTTTCCTCCAGTACAAAATGTGTGCAATAAGATCTGTGATACTAGTAAATGTACTATGTAACTCCCTTTA... |
Task1_train_46781 | Consider a variant on Chromosome 19. Determine its clinical classification and disease relevance. | Benign | TTCGAGACCAGCCTGGCAAACATGGCGAAGTCGCATCTCTACTAAAAATAAAAAAATTAGCTGGGCATGTTGGAGGACACCTGTAATCCCAGCTACTCAGGAAGCTGAGGTAGGAGAATGGCTTAAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATCATGGCACTGTACTCCAGCTTGGATGACAAGCATGAAACTTCATCTCAAAAAAAAAAATATTGAAAACTTGTTATAGGATTTGCCACATTCCTCAAACTTGTAGGATTTTTGTCCAGCATGAATTATGTGTAAGAAGGGTTCAGAACTTCCTAAAAGCGTT... | TTCGAGACCAGCCTGGCAAACATGGCGAAGTCGCATCTCTACTAAAAATAAAAAAATTAGCTGGGCATGTTGGAGGACACCTGTAATCCCAGCTACTCAGGAAGCTGAGGTAGGAGAATGGCTTAAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATCATGGCACTGTACTCCAGCTTGGATGACAAGCATGAAACTTCATCTCAAAAAAAAAAATATTGAAAACTTGTTATAGGATTTGCCACATTCCTCAAACTTGTAGGATTTTTGTCCAGCATGAATTATGTGTAAGAAGGGTTCAGAACTTCCTAAAAGCGTT... |
Task1_train_46782 | A mutation located on Chromosome 19 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | ATCAAAAATCAGCTAAGAAAGAATATAAGCCATAACTAAAATTGGGGTCATATTTATAGATAAATACACATACAAATGTAATCTGATTATGATAGATATGCATAATTTATCTCTTAATTAAACCTTAAATTGACTTAAAGTGTACAAAAAGAACTGCAAATTGTCTAAAATTATAATACATAAGTAAAACCAAAACACCCAATAAACTAATCTTAAGAAACCTACACTGAGGCCAGAGGCAGTAGGTCACATCTGTAATCCCAGCACTTTGGGAGACCAAAGTGTGCAAATCCTGAGGCCAGCAGTTCCAGACCACATTG... | ATCAAAAATCAGCTAAGAAAGAATATAAGCCATAACTAAAATTGGGGTCATATTTATAGATAAATACACATACAAATGTAATCTGATTATGATAGATATGCATAATTTATCTCTTAATTAAACCTTAAATTGACTTAAAGTGTACAAAAAGAACTGCAAATTGTCTAAAATTATAATACATAAGTAAAACCAAAACACCCAATAAACTAATCTTAAGAAACCTACACTGAGGCCAGAGGCAGTAGGTCACATCTGTAATCCCAGCACTTTGGGAGACCAAAGTGTGCAAATCCTGAGGCCAGCAGTTCCAGACCACATTG... |
Task1_train_46783 | Consider this mutation on Chromosome 19. Is this a benign change or a disease-causing variant? | Benign | AGTTAAGTAAGTAAATAAAATATAAGTTAAGTTCACACATCATCTAACAATTTTTAAATATATTGCATTTTATTACGTAACAGTAAAATTAGTAAAATAATTGATATACTTTAATTTATAATTTCTTTCTCTCAGTATAATGTAGAAAAGTATTACTCTGAACACCTACCTTAAACATTACTTAATATAGGTTAACTACAATGAGCCTCTCCACTTATATTTTCGTCATGCATCTTACATTTTAATGTCCTTACTGTTTTATAGAAAAGGTCATAAAGAATGCCCAACTCATAAAGAATCTCTAATATCTCTGATGCAGC... | AGTTAAGTAAGTAAATAAAATATAAGTTAAGTTCACACATCATCTAACAATTTTTAAATATATTGCATTTTATTACGTAACAGTAAAATTAGTAAAATAATTGATATACTTTAATTTATAATTTCTTTCTCTCAGTATAATGTAGAAAAGTATTACTCTGAACACCTACCTTAAACATTACTTAATATAGGTTAACTACAATGAGCCTCTCCACTTATATTTTCGTCATGCATCTTACATTTTAATGTCCTTACTGTTTTATAGAAAAGGTCATAAAGAATGCCCAACTCATAAAGAATCTCTAATATCTCTGATGCAGC... |
Task1_train_46784 | Here is a variant on Chromosome 19. Please identify whether it is a benign mutation or associated with a disorder. | Benign | AGGCTGAGGTGGGTGGATCATGTGAGGTCAGGGGTTGGATACCAGCCTGACAAACATGGTGTAACCTTGTCTCTACTAAAAATACAAAAGTTAGCTGGGCATGGGGGTGGGCACCTGTAATCCCCCTTACTTGGGAGGTTGAGGCAGGAGAATGGATTGAACCCAGAAGGCGGAGGTTGCAGTGAGCCGAGACTGTGCTATTGCACACCAGACTGGGTGACAAGAGTTGAAACTCCATCTCAAAAAAAAAAAAAAAAAGACAGAACTTGTTATATGCTTTGCCACATTCTTCACACTTGTAGGGTTTCTTTCCAGTATGA... | AGGCTGAGGTGGGTGGATCATGTGAGGTCAGGGGTTGGATACCAGCCTGACAAACATGGTGTAACCTTGTCTCTACTAAAAATACAAAAGTTAGCTGGGCATGGGGGTGGGCACCTGTAATCCCCCTTACTTGGGAGGTTGAGGCAGGAGAATGGATTGAACCCAGAAGGCGGAGGTTGCAGTGAGCCGAGACTGTGCTATTGCACACCAGACTGGGTGACAAGAGTTGAAACTCCATCTCAAAAAAAAAAAAAAAAAGACAGAACTTGTTATATGCTTTGCCACATTCTTCACACTTGTAGGGTTTCTTTCCAGTATGA... |
Task1_train_46785 | A variant on Chromosome 19 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TGAGGTGGGTGGATCATGTGAGGTCAGGGGTTGGATACCAGCCTGACAAACATGGTGTAACCTTGTCTCTACTAAAAATACAAAAGTTAGCTGGGCATGGGGGTGGGCACCTGTAATCCCCCTTACTTGGGAGGTTGAGGCAGGAGAATGGATTGAACCCAGAAGGCGGAGGTTGCAGTGAGCCGAGACTGTGCTATTGCACACCAGACTGGGTGACAAGAGTTGAAACTCCATCTCAAAAAAAAAAAAAAAAAGACAGAACTTGTTATATGCTTTGCCACATTCTTCACACTTGTAGGGTTTCTTTCCAGTATGAATTA... | TGAGGTGGGTGGATCATGTGAGGTCAGGGGTTGGATACCAGCCTGACAAACATGGTGTAACCTTGTCTCTACTAAAAATACAAAAGTTAGCTGGGCATGGGGGTGGGCACCTGTAATCCCCCTTACTTGGGAGGTTGAGGCAGGAGAATGGATTGAACCCAGAAGGCGGAGGTTGCAGTGAGCCGAGACTGTGCTATTGCACACCAGACTGGGTGACAAGAGTTGAAACTCCATCTCAAAAAAAAAAAAAAAAAGACAGAACTTGTTATATGCTTTGCCACATTCTTCACACTTGTAGGGTTTCTTTCCAGTATGAATTA... |
Task1_train_46786 | Given a variant located on Chromosome 19, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TCAGCCATCCCTGACCAAAAATGACTTTATGAGACAACCAGGCATTATGGTTCACATCTGTAATGACAGCTACATGGTACATTACTGTTGGAGAGAAATGCTTCAGGCCAGGATTTTGAGACCAGCCTTGGTTATGTAGCAAGACGTCATCTCCAAAATAAGTGCCTCTAAGAGAGATGTGAGATCCAGGGATGCAGTTGTGAAACCCTATTAAAGCTGAAGTTCGAGACGTGTTCTATTCAGAAGGCAGGCCCTCATTCAGGTGGGAAATTACAGGACCCCTGTTCTTGGCTACAGACCAGGATAGGGTTCACCCAACT... | TCAGCCATCCCTGACCAAAAATGACTTTATGAGACAACCAGGCATTATGGTTCACATCTGTAATGACAGCTACATGGTACATTACTGTTGGAGAGAAATGCTTCAGGCCAGGATTTTGAGACCAGCCTTGGTTATGTAGCAAGACGTCATCTCCAAAATAAGTGCCTCTAAGAGAGATGTGAGATCCAGGGATGCAGTTGTGAAACCCTATTAAAGCTGAAGTTCGAGACGTGTTCTATTCAGAAGGCAGGCCCTCATTCAGGTGGGAAATTACAGGACCCCTGTTCTTGGCTACAGACCAGGATAGGGTTCACCCAACT... |
Task1_train_46787 | A variant found on Chromosome 19 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GATTCACTTGCTTAAATAGGTCTCTGACAGACTTTTTTTTACTATATAGCTAATTATTTTTCTCTTCATTATTAAGTTTCATTATGCAGCTGATGTGAACAAACAATCATTTAATCTGGCAGCTGTTCTTTTTTCTTTTTTTCTACATATTTTTCTTTGGAAAATTAAGGCTCTTATCTTTGTTTACAGGCCAGAAAAACTGGAAAAAACACAGGCTCTTCCACTTACTGGATGTTTGACAAAATATTCTTCTTGGGCCAAAAACATTGACATTATTGGTTAGCTTGCTAGAAATTCAAAAAATCAGACTTTATTCCAGA... | GATTCACTTGCTTAAATAGGTCTCTGACAGACTTTTTTTTACTATATAGCTAATTATTTTTCTCTTCATTATTAAGTTTCATTATGCAGCTGATGTGAACAAACAATCATTTAATCTGGCAGCTGTTCTTTTTTCTTTTTTTCTACATATTTTTCTTTGGAAAATTAAGGCTCTTATCTTTGTTTACAGGCCAGAAAAACTGGAAAAAACACAGGCTCTTCCACTTACTGGATGTTTGACAAAATATTCTTCTTGGGCCAAAAACATTGACATTATTGGTTAGCTTGCTAGAAATTCAAAAAATCAGACTTTATTCCAGA... |
Task1_train_46788 | This genomic variant is located on Chromosome 19. Can you determine its pathogenicity and name any linked disease? | Benign | GGTGTGTACATTTTTAAAGAAATTTTCCAATTATGTTTTGTATTTTTATATCCACGATTTTTGTTTTTTGCTATTTAAATGTTTCTGGTTGTTATTCTCATTTTTCTGATCTTCAGTAGTTGCCTGTGTTCCTATTTAACTTACTGAATATTATTCAATTTATTTTATTTTATTTATTTATTTTATTATTATTTTCTGAGACAGAGTCTGTCTCTGTCACCTCAACTGGAGTGCAGTGGTGCAGGCTCACTGCAACCTCCATCTCCCAGGTTCAAGCAATTCTCTTGCCTCAGCCTCCTCAGTAACTGGGATTATAGGTG... | GGTGTGTACATTTTTAAAGAAATTTTCCAATTATGTTTTGTATTTTTATATCCACGATTTTTGTTTTTTGCTATTTAAATGTTTCTGGTTGTTATTCTCATTTTTCTGATCTTCAGTAGTTGCCTGTGTTCCTATTTAACTTACTGAATATTATTCAATTTATTTTATTTTATTTATTTATTTTATTATTATTTTCTGAGACAGAGTCTGTCTCTGTCACCTCAACTGGAGTGCAGTGGTGCAGGCTCACTGCAACCTCCATCTCCCAGGTTCAAGCAATTCTCTTGCCTCAGCCTCCTCAGTAACTGGGATTATAGGTG... |
Task1_train_46789 | This variant is located on Chromosome 19. Evaluate its biological effect and specify any disease association. | Benign | TGCCTCAGCCTCCTCAGTAACTGGGATTATAGGTGCTCACAACCACACTTGGCTATTTTTTTATATTTTTAGTAGAGATAAGGTTTCACCATGTTGGCCAGGCTAATCTTGAACCTCTGACCTCAAATGATCCATCCACCTTGGCCTCTCAAAGTGCTGGGATTACAGGTGTGAGCCATCCTGCCCACCCTATTTTATTATATTTTTGAGACAGGCTTCCTCTGTTGTCCAGGCTGTAGTGCAGAGGTACAATCTTCACTCACTGATGGGGCCATGTTGCTCTAATATTTTGTATTCATTGTAATCTTTGATTGAGCTTT... | TGCCTCAGCCTCCTCAGTAACTGGGATTATAGGTGCTCACAACCACACTTGGCTATTTTTTTATATTTTTAGTAGAGATAAGGTTTCACCATGTTGGCCAGGCTAATCTTGAACCTCTGACCTCAAATGATCCATCCACCTTGGCCTCTCAAAGTGCTGGGATTACAGGTGTGAGCCATCCTGCCCACCCTATTTTATTATATTTTTGAGACAGGCTTCCTCTGTTGTCCAGGCTGTAGTGCAGAGGTACAATCTTCACTCACTGATGGGGCCATGTTGCTCTAATATTTTGTATTCATTGTAATCTTTGATTGAGCTTT... |
Task1_train_46790 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CGTGGCATATAAGAGACTGCGCAGTCTGGCTGCTTTTTCATTGTTTTGGGGGACACACAAATATCTGCATAATTTTGAAAAAGTCTATGTTAAGCAATATTTTTAATTGTATTTTTGCATCATGTTTGAAATATGTGAGTAGTGGTTTCTGTTCCATTGGGGGTTTTTTTGTTTGTTTTTCTGCACATTCCATCCTGTTTGTATTACTACATTCTTGAAATATAGTTTGAAATTATAAAGTATGATGCCCCTATGCTTTGTTCTTTTACCTCAAGATTGCTTTGGCTATTCAAAGTTTATTATAGTTTCATGTATGTTTT... | CGTGGCATATAAGAGACTGCGCAGTCTGGCTGCTTTTTCATTGTTTTGGGGGACACACAAATATCTGCATAATTTTGAAAAAGTCTATGTTAAGCAATATTTTTAATTGTATTTTTGCATCATGTTTGAAATATGTGAGTAGTGGTTTCTGTTCCATTGGGGGTTTTTTTGTTTGTTTTTCTGCACATTCCATCCTGTTTGTATTACTACATTCTTGAAATATAGTTTGAAATTATAAAGTATGATGCCCCTATGCTTTGTTCTTTTACCTCAAGATTGCTTTGGCTATTCAAAGTTTATTATAGTTTCATGTATGTTTT... |
Task1_train_46791 | A change on Chromosome 19 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | ATAATCTCGGCTCACTGCAACCTCTGCCTTTCAGGTTCAGGAGTAGCTGGGATTACAGGCACCCACCTCCACACCTGGCTAATTTTTTGTATTCTTGGTAGAGACGGGGTTTCAGTATGTTGGCCAGACTGGTCTTGAACTCCTGACCTCATGATCCACCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGACGTGAGCCACCTTGCTGGCCTATTATGTTTTTAAATCAGGAAGTATAATGCCTCTGTTCTTTTTCATGGGTGTTTGGCTATAGTTTATAATCAAATTTTAAACAATATTTCTGTAAAAATATGTGGT... | ATAATCTCGGCTCACTGCAACCTCTGCCTTTCAGGTTCAGGAGTAGCTGGGATTACAGGCACCCACCTCCACACCTGGCTAATTTTTTGTATTCTTGGTAGAGACGGGGTTTCAGTATGTTGGCCAGACTGGTCTTGAACTCCTGACCTCATGATCCACCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGACGTGAGCCACCTTGCTGGCCTATTATGTTTTTAAATCAGGAAGTATAATGCCTCTGTTCTTTTTCATGGGTGTTTGGCTATAGTTTATAATCAAATTTTAAACAATATTTCTGTAAAAATATGTGGT... |
Task1_train_46792 | This mutation occurs on Chromosome 19. Does this change lead to a known medical condition, or is it benign? | Benign | CAGGTATTCCTCTATGTGCAAAATAATATATTCTGTAACGTTGTCTAAGTTTTCTGTTTTCTTATTGATCTTTTGTCTGAATTTTCTATTTATTATTAAAAATGGGGTCTTGATGTCTACAATTATTATGTTGCTATGTATTTCTTGTTTCACTTTTGTCAATATTTGCTTTACGTATTTTGGAGCCCTAATGTTGTATATACATATACACATAAATAAATAGGCATAATAGTTTTAGATTCCTGGTAAATTGATCCATTTTACTATTGTATAATATCAGTCTTTGTCTCATGCTAGTACTTGACTTAAAGCATATAATG... | CAGGTATTCCTCTATGTGCAAAATAATATATTCTGTAACGTTGTCTAAGTTTTCTGTTTTCTTATTGATCTTTTGTCTGAATTTTCTATTTATTATTAAAAATGGGGTCTTGATGTCTACAATTATTATGTTGCTATGTATTTCTTGTTTCACTTTTGTCAATATTTGCTTTACGTATTTTGGAGCCCTAATGTTGTATATACATATACACATAAATAAATAGGCATAATAGTTTTAGATTCCTGGTAAATTGATCCATTTTACTATTGTATAATATCAGTCTTTGTCTCATGCTAGTACTTGACTTAAAGCATATAATG... |
Task1_train_46793 | A variant found on Chromosome 19 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CTGAATTTTCTATTTATTATTAAAAATGGGGTCTTGATGTCTACAATTATTATGTTGCTATGTATTTCTTGTTTCACTTTTGTCAATATTTGCTTTACGTATTTTGGAGCCCTAATGTTGTATATACATATACACATAAATAAATAGGCATAATAGTTTTAGATTCCTGGTAAATTGATCCATTTTACTATTGTATAATATCAGTCTTTGTCTCATGCTAGTACTTGACTTAAAGCATATAATGTCTAATATAATTATGAGTGTCTTACTCAATTGTGGTTATATTTGCATGTAATAAAAAGTTTTTCCATTCTGTTACT... | CTGAATTTTCTATTTATTATTAAAAATGGGGTCTTGATGTCTACAATTATTATGTTGCTATGTATTTCTTGTTTCACTTTTGTCAATATTTGCTTTACGTATTTTGGAGCCCTAATGTTGTATATACATATACACATAAATAAATAGGCATAATAGTTTTAGATTCCTGGTAAATTGATCCATTTTACTATTGTATAATATCAGTCTTTGTCTCATGCTAGTACTTGACTTAAAGCATATAATGTCTAATATAATTATGAGTGTCTTACTCAATTGTGGTTATATTTGCATGTAATAAAAAGTTTTTCCATTCTGTTACT... |
Task1_train_46794 | This variant is located on Chromosome 19. Evaluate its biological effect and specify any disease association. | Benign | TAACTTAAGATGTGTTGTGTAATATTACTTAGACCTCTTCTGCTCTCATTTGGTTAAAATTTGCATGGAATGTCTACTTCCATCTTGCCACTTTCAGTCTTTCTTTATCATTAGATCGCAACTGACTCTTGTAGAAAGGCAAGTTGAATCCTGGTTTTTAATTTTTTTAATAAATCCCTTTATTGAAAGTATGTCTTTTAATTAAAAAGTTAACTTTATGTATATTTAATTTTCTGAAACAGACTTACAAATGTTATTTTATTGTTTTAGTTGATTCTTGTTTCTTTGTTCCCAATTTTCTCTCTCTCTTTCTTTGTGTC... | TAACTTAAGATGTGTTGTGTAATATTACTTAGACCTCTTCTGCTCTCATTTGGTTAAAATTTGCATGGAATGTCTACTTCCATCTTGCCACTTTCAGTCTTTCTTTATCATTAGATCGCAACTGACTCTTGTAGAAAGGCAAGTTGAATCCTGGTTTTTAATTTTTTTAATAAATCCCTTTATTGAAAGTATGTCTTTTAATTAAAAAGTTAACTTTATGTATATTTAATTTTCTGAAACAGACTTACAAATGTTATTTTATTGTTTTAGTTGATTCTTGTTTCTTTGTTCCCAATTTTCTCTCTCTCTTTCTTTGTGTC... |
Task1_train_46795 | Chromosome 19 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TCAGTCTTTCTTTATCATTAGATCGCAACTGACTCTTGTAGAAAGGCAAGTTGAATCCTGGTTTTTAATTTTTTTAATAAATCCCTTTATTGAAAGTATGTCTTTTAATTAAAAAGTTAACTTTATGTATATTTAATTTTCTGAAACAGACTTACAAATGTTATTTTATTGTTTTAGTTGATTCTTGTTTCTTTGTTCCCAATTTTCTCTCTCTCTTTCTTTGTGTCATTTTTATTTTTGTACTAATATGCTTTCACTTTTTAAAATTTTCTTTTATATCTCTATACAGATTTTTTTGTGGTACCTTGGGGTTTACATAA... | TCAGTCTTTCTTTATCATTAGATCGCAACTGACTCTTGTAGAAAGGCAAGTTGAATCCTGGTTTTTAATTTTTTTAATAAATCCCTTTATTGAAAGTATGTCTTTTAATTAAAAAGTTAACTTTATGTATATTTAATTTTCTGAAACAGACTTACAAATGTTATTTTATTGTTTTAGTTGATTCTTGTTTCTTTGTTCCCAATTTTCTCTCTCTCTTTCTTTGTGTCATTTTTATTTTTGTACTAATATGCTTTCACTTTTTAAAATTTTCTTTTATATCTCTATACAGATTTTTTTGTGGTACCTTGGGGTTTACATAA... |
Task1_train_46796 | An alteration has been detected on Chromosome 19. Is it pathogenic, and if so, what disease is involved? | Benign | CTCTCTCTCTTTCTTTGTGTCATTTTTATTTTTGTACTAATATGCTTTCACTTTTTAAAATTTTCTTTTATATCTCTATACAGATTTTTTTGTGGTACCTTGGGGTTTACATAAAATCTCTAAAAGATGCAACAGTATATTTAATTATGGTAAAAAATGAACTTTAGTTGTATACAAAAAATCTTTCTCATTATATCTGCCCTCAACTTTCTTATTGATGTTGCTAATTATATCTTTATGTTGTAAGTACATTAATGAGTGTTTATAATAATTAGTGTTTTTATTTTTCAACTTTTAGAGAATAACTAAAAATGTTTTCT... | CTCTCTCTCTTTCTTTGTGTCATTTTTATTTTTGTACTAATATGCTTTCACTTTTTAAAATTTTCTTTTATATCTCTATACAGATTTTTTTGTGGTACCTTGGGGTTTACATAAAATCTCTAAAAGATGCAACAGTATATTTAATTATGGTAAAAAATGAACTTTAGTTGTATACAAAAAATCTTTCTCATTATATCTGCCCTCAACTTTCTTATTGATGTTGCTAATTATATCTTTATGTTGTAAGTACATTAATGAGTGTTTATAATAATTAGTGTTTTTATTTTTCAACTTTTAGAGAATAACTAAAAATGTTTTCT... |
Task1_train_46797 | Chromosome 19 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TGTTTATAATAATTAGTGTTTTTATTTTTCAACTTTTAGAGAATAACTAAAAATGTTTTCTGCACCATTATGATAATGCTAAGGAATTCTAATTTTGGATATGTGCATATCTTTCCCAGAAAGTTATGCATTTTTATGTAATAATATGTTGTTTTCTTACATTATGTTATTTTTAGCATCTTTGATATGTAGGGCATATGCAGTGCCAATACACTTTTTTTTTTTTTTTTTTTTTTTTTTTTTACTAATTTCAGGACTATTACAATATCACATAGTTCCCTTCTCGCTTGCAAAATTTTCATGACAAATTTACTAGTAAT... | TGTTTATAATAATTAGTGTTTTTATTTTTCAACTTTTAGAGAATAACTAAAAATGTTTTCTGCACCATTATGATAATGCTAAGGAATTCTAATTTTGGATATGTGCATATCTTTCCCAGAAAGTTATGCATTTTTATGTAATAATATGTTGTTTTCTTACATTATGTTATTTTTAGCATCTTTGATATGTAGGGCATATGCAGTGCCAATACACTTTTTTTTTTTTTTTTTTTTTTTTTTTTTACTAATTTCAGGACTATTACAATATCACATAGTTCCCTTCTCGCTTGCAAAATTTTCATGACAAATTTACTAGTAAT... |
Task1_train_46798 | Assess the clinical impact of this variant found on Chromosome 19. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CTTTGGATGGGATGCTTGTGAGGATTTTTTTGTTCATGCTGTTTTTGTTGTTGCTTTCTGTTTGTTTTTCTAACCATCAGGCCACTTTTCTGTAGCACTGTTGTGATTTGCTTGGGATCTACTTCAGACCCTATTTGCCTGGGTTTCTCTCACACCTGGAGGTGTCAACCAGTGGAGCCTGCAGAATAGCAGAGAGGACTGCTTGCTCCTTCCTCTGGGGTCTTTGTCCCAGAAGGGGAATGATCTGATGACAGTGGGAACACTACTTTATAAGTTGTCTGACGATGTCTGTTGTGGGGGTCTCACCCAGTCAGGATGCA... | CTTTGGATGGGATGCTTGTGAGGATTTTTTTGTTCATGCTGTTTTTGTTGTTGCTTTCTGTTTGTTTTTCTAACCATCAGGCCACTTTTCTGTAGCACTGTTGTGATTTGCTTGGGATCTACTTCAGACCCTATTTGCCTGGGTTTCTCTCACACCTGGAGGTGTCAACCAGTGGAGCCTGCAGAATAGCAGAGAGGACTGCTTGCTCCTTCCTCTGGGGTCTTTGTCCCAGAAGGGGAATGATCTGATGACAGTGGGAACACTACTTTATAAGTTGTCTGACGATGTCTGTTGTGGGGGTCTCACCCAGTCAGGATGCA... |
Task1_train_46799 | With a mutation on Chromosome 19, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | ACAGTTCACTGACTATCTTATAAGACTGTGCTTGTAAATGACATGCCATTTTTATCTTGCAGCTCCATTCTCTTCTTGTCTGTGGTTTTTGAAATTGTGCTTATATATGTGTTTGTTATAAATATCTTTGTGTGTATCCTAATTGTTTGTTGAGCTTCTTCATTTTGACAATATTTTTTCTTTCAGAATTTTTGAGTTATATTTTCTTTTGATATTTTTTACCTTTACAATTTCTGTTTTTTGGATATTTTAAATATTTTTTTCTTATCAGTTTTTTCTGGTTTTCTATAGTTCTCTGTATTCCTATTTTACTCATTGAG... | ACAGTTCACTGACTATCTTATAAGACTGTGCTTGTAAATGACATGCCATTTTTATCTTGCAGCTCCATTCTCTTCTTGTCTGTGGTTTTTGAAATTGTGCTTATATATGTGTTTGTTATAAATATCTTTGTGTGTATCCTAATTGTTTGTTGAGCTTCTTCATTTTGACAATATTTTTTCTTTCAGAATTTTTGAGTTATATTTTCTTTTGATATTTTTTACCTTTACAATTTCTGTTTTTTGGATATTTTAAATATTTTTTTCTTATCAGTTTTTTCTGGTTTTCTATAGTTCTCTGTATTCCTATTTTACTCATTGAG... |
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