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_45500 | This sequence change occurs on Chromosome 17. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CGCCCGGCCACGGGAGCACCTCCGGGAAGGGCCCAGCCGGCCTCTCCCGCTAGCCTCTAGTCCAGTCCTGGGGCCCTCAATTACGGGGAGGCCACCCCTCTCCCGTGTGGGGCCCAGTCGTCCAGAGGCCTGGGGCCCATTGTTGCTGAGAAGTCGGCTGCAGTGTTCTCGGGGATCTGGAGGCCGCCTGCGGCTTGGGGGCTTCTCAGGGGAGCCCCCTCCTCTCCTCCGGCTGCTTCCACCAACTAATCCAGGCATGTCTTCCAGGCAGTCTCCAGCCCTGGAGGACTCAGGAGACAAGGGACACTGGCCAGGTCTTC... | CGCCCGGCCACGGGAGCACCTCCGGGAAGGGCCCAGCCGGCCTCTCCCGCTAGCCTCTAGTCCAGTCCTGGGGCCCTCAATTACGGGGAGGCCACCCCTCTCCCGTGTGGGGCCCAGTCGTCCAGAGGCCTGGGGCCCATTGTTGCTGAGAAGTCGGCTGCAGTGTTCTCGGGGATCTGGAGGCCGCCTGCGGCTTGGGGGCTTCTCAGGGGAGCCCCCTCCTCTCCTCCGGCTGCTTCCACCAACTAATCCAGGCATGTCTTCCAGGCAGTCTCCAGCCCTGGAGGACTCAGGAGACAAGGGACACTGGCCAGGTCTTC... |
Task1_train_45501 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | TCCTGGGGCCCTCAATTACGGGGAGGCCACCCCTCTCCCGTGTGGGGCCCAGTCGTCCAGAGGCCTGGGGCCCATTGTTGCTGAGAAGTCGGCTGCAGTGTTCTCGGGGATCTGGAGGCCGCCTGCGGCTTGGGGGCTTCTCAGGGGAGCCCCCTCCTCTCCTCCGGCTGCTTCCACCAACTAATCCAGGCATGTCTTCCAGGCAGTCTCCAGCCCTGGAGGACTCAGGAGACAAGGGACACTGGCCAGGTCTTCGGGGCTGACCACTGTCACAGCCCAGCCCCAGCAATGCAGGTTCAGGCGGGCCAGGGTCTCGGGAA... | TCCTGGGGCCCTCAATTACGGGGAGGCCACCCCTCTCCCGTGTGGGGCCCAGTCGTCCAGAGGCCTGGGGCCCATTGTTGCTGAGAAGTCGGCTGCAGTGTTCTCGGGGATCTGGAGGCCGCCTGCGGCTTGGGGGCTTCTCAGGGGAGCCCCCTCCTCTCCTCCGGCTGCTTCCACCAACTAATCCAGGCATGTCTTCCAGGCAGTCTCCAGCCCTGGAGGACTCAGGAGACAAGGGACACTGGCCAGGTCTTCGGGGCTGACCACTGTCACAGCCCAGCCCCAGCAATGCAGGTTCAGGCGGGCCAGGGTCTCGGGAA... |
Task1_train_45502 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | AGGGTCAGCCCCAGCCACAGTAACAAGGGTCCTTTGGCAGAGGGAGAAAGAGCCATGTCCTAAATGGGGGAGGCACACCATGGCTCAGGGGCAGGGTGGGAGAAGGGAGATGGGAGCCACATGGGACAGAGAAATCCTAGAAGAAAAACAGACACATAGCACAGCCAAAGGTGTGAGAGCAGGACCAGAGCAGAGGACAGGCAGAGAGGGCAACTGGATTTGCGCTGGCAAAAGGTAGGGAGACAGGCCTCAATTCTCTGAAGTGACACAGTGTGTCCCCAAACCCCTACCTCAGCCCTGGGCCTCAGCCCAGACCCTGG... | AGGGTCAGCCCCAGCCACAGTAACAAGGGTCCTTTGGCAGAGGGAGAAAGAGCCATGTCCTAAATGGGGGAGGCACACCATGGCTCAGGGGCAGGGTGGGAGAAGGGAGATGGGAGCCACATGGGACAGAGAAATCCTAGAAGAAAAACAGACACATAGCACAGCCAAAGGTGTGAGAGCAGGACCAGAGCAGAGGACAGGCAGAGAGGGCAACTGGATTTGCGCTGGCAAAAGGTAGGGAGACAGGCCTCAATTCTCTGAAGTGACACAGTGTGTCCCCAAACCCCTACCTCAGCCCTGGGCCTCAGCCCAGACCCTGG... |
Task1_train_45503 | This alteration occurs on Chromosome 17. Is it associated with a disease or is it a benign variant? | Benign | GAAGGGAGATGGGAGCCACATGGGACAGAGAAATCCTAGAAGAAAAACAGACACATAGCACAGCCAAAGGTGTGAGAGCAGGACCAGAGCAGAGGACAGGCAGAGAGGGCAACTGGATTTGCGCTGGCAAAAGGTAGGGAGACAGGCCTCAATTCTCTGAAGTGACACAGTGTGTCCCCAAACCCCTACCTCAGCCCTGGGCCTCAGCCCAGACCCTGGGTCTCCTCCTTGGCACATCTCGGTATTTGGCGCCTGCTGGGCCCGTGCTCCCTGGGTGGAGCTGGAGGCCGGACAGGCCTCTCCTGCAGTCCACTCGGCCT... | GAAGGGAGATGGGAGCCACATGGGACAGAGAAATCCTAGAAGAAAAACAGACACATAGCACAGCCAAAGGTGTGAGAGCAGGACCAGAGCAGAGGACAGGCAGAGAGGGCAACTGGATTTGCGCTGGCAAAAGGTAGGGAGACAGGCCTCAATTCTCTGAAGTGACACAGTGTGTCCCCAAACCCCTACCTCAGCCCTGGGCCTCAGCCCAGACCCTGGGTCTCCTCCTTGGCACATCTCGGTATTTGGCGCCTGCTGGGCCCGTGCTCCCTGGGTGGAGCTGGAGGCCGGACAGGCCTCTCCTGCAGTCCACTCGGCCT... |
Task1_train_45504 | A genomic variant on Chromosome 17 is under review. What is the biological outcome — benign or pathogenic? | Benign | TTTTTCCTCTCTGTGGACAAACAGAACATTTGAAGATTTCTGGACAGTTTAGTGTAAGGCAGATGACGCTGGCAGCAATAGGGAGGGTAGGTGAGCAGTGGAGCTGTGGTGCACAACTTTATGGGACATACTGGATGGGCAGCACTCAGCCTTCGAGGCCCTGTAAGAGGGAAGGGAAGAGCTAGGAGGCTCCTGCATGGATCTTTAGGGTATACCTAAGACACTGGCAGGGCCATCAGTACTGGACTTGAAAAGAACATGATAAAGCTAGCCAAGATACAGTTAACAGAATCTGGCACTGATTAGATGTGAAAGGCAAG... | TTTTTCCTCTCTGTGGACAAACAGAACATTTGAAGATTTCTGGACAGTTTAGTGTAAGGCAGATGACGCTGGCAGCAATAGGGAGGGTAGGTGAGCAGTGGAGCTGTGGTGCACAACTTTATGGGACATACTGGATGGGCAGCACTCAGCCTTCGAGGCCCTGTAAGAGGGAAGGGAAGAGCTAGGAGGCTCCTGCATGGATCTTTAGGGTATACCTAAGACACTGGCAGGGCCATCAGTACTGGACTTGAAAAGAACATGATAAAGCTAGCCAAGATACAGTTAACAGAATCTGGCACTGATTAGATGTGAAAGGCAAG... |
Task1_train_45505 | A variant was discovered on Chromosome 17. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | ATGTTAAAGTTGAGAATTTACGTGATCACTGCTTATGATATAGGGATGCACTGAATCCCCAAGAAATTAAGGTCAGTCTTATTAATAATGATGTGTTGAAGGGAAGTCCTCCTTGTTCTTTTACCACAGGGGAAGAGAAGAAAACCTAAGGCTCCACAGGGCTGCTGGGAACCACCTGTGGTTTCTCTCTCTCTCTTTTTTCTCGTTGTTCACATAGCTCTTCTTATATAGCCTCGTATTATGGTTATGTGTAATTATTTCTACTATAGCTCCCCCCGAGGAACACTTCTTAGCCTTCTTTGTATTTAGAACTAATACTG... | ATGTTAAAGTTGAGAATTTACGTGATCACTGCTTATGATATAGGGATGCACTGAATCCCCAAGAAATTAAGGTCAGTCTTATTAATAATGATGTGTTGAAGGGAAGTCCTCCTTGTTCTTTTACCACAGGGGAAGAGAAGAAAACCTAAGGCTCCACAGGGCTGCTGGGAACCACCTGTGGTTTCTCTCTCTCTCTTTTTTCTCGTTGTTCACATAGCTCTTCTTATATAGCCTCGTATTATGGTTATGTGTAATTATTTCTACTATAGCTCCCCCCGAGGAACACTTCTTAGCCTTCTTTGTATTTAGAACTAATACTG... |
Task1_train_45506 | Located on Chromosome 17, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TATATAGCCTCGTATTATGGTTATGTGTAATTATTTCTACTATAGCTCCCCCCGAGGAACACTTCTTAGCCTTCTTTGTATTTAGAACTAATACTGAGCTGTGAGCATTGGTAGAACTAAACCAGTTATTAAAATTTAGAAACACTTATGTTTGAGCTACTACCCCGGGGACCATTCCAAATGCCTCTTTTTTTTTTTTTTTTTTTTTTTTTGAGATGGAGTCTCACCCTGTTACCCAGGCTGGAGTGCAGTGGCGCCATCTTGGCTCACTGCAACTTCCGCCTCTTAGGTTCACGCGATTCTCCTGCCTCAGCCTCCTG... | TATATAGCCTCGTATTATGGTTATGTGTAATTATTTCTACTATAGCTCCCCCCGAGGAACACTTCTTAGCCTTCTTTGTATTTAGAACTAATACTGAGCTGTGAGCATTGGTAGAACTAAACCAGTTATTAAAATTTAGAAACACTTATGTTTGAGCTACTACCCCGGGGACCATTCCAAATGCCTCTTTTTTTTTTTTTTTTTTTTTTTTTGAGATGGAGTCTCACCCTGTTACCCAGGCTGGAGTGCAGTGGCGCCATCTTGGCTCACTGCAACTTCCGCCTCTTAGGTTCACGCGATTCTCCTGCCTCAGCCTCCTG... |
Task1_train_45507 | Chromosome 17 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | ATGGCTGTAGCTAATCTATTTGACCCTGAGTAGCCTGTGAGCTCAGAGTTTGGGGGATCAAGGACGTGCCTAAGCTGCCTGTGCTCTGGGACTCCTTTGTTCCCTCCAGTCAGGTTGCCTGCCCTGGGAGGGCCACTATGCGTGTCAATCCCTAAACCTCCCCTCAGCCATTTGGAGCTCTTTCACCCAGGGCCACTGTTAGCCCATAGGGCACCTGTGGGTACCTTAGAAAAAGGTTCTCTTTCCTCAAGATATTTATTTCACTTTCATCTTTTAGAAAATTATGTTAACATACTGATTTTGTTAGAATAGAATATTTT... | ATGGCTGTAGCTAATCTATTTGACCCTGAGTAGCCTGTGAGCTCAGAGTTTGGGGGATCAAGGACGTGCCTAAGCTGCCTGTGCTCTGGGACTCCTTTGTTCCCTCCAGTCAGGTTGCCTGCCCTGGGAGGGCCACTATGCGTGTCAATCCCTAAACCTCCCCTCAGCCATTTGGAGCTCTTTCACCCAGGGCCACTGTTAGCCCATAGGGCACCTGTGGGTACCTTAGAAAAAGGTTCTCTTTCCTCAAGATATTTATTTCACTTTCATCTTTTAGAAAATTATGTTAACATACTGATTTTGTTAGAATAGAATATTTT... |
Task1_train_45508 | A variant on Chromosome 17 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | AATGAATACTAAGCTAGTGAAAAAACTTATTTAAAGACCTAAACGAAGCATATGTGGACAGAAAGGAGATGACTAAAAATTGCCAATGACATAAAACTATCCACTGTAAAGGCTGAAAGTCTTTGCTAAGTTATGATGAAATTCCCTCTTCACAAAGTAAAAGCAATACTTAATGTATAATGATAGGATCAAAGTTAATAGTTTAAAAAACAAAATAGATTGGTAAGATTTGCCAGAGTGAGAAAAACGATAGAACAATAGAAGACATGATAAAGATTGATAAAATAATGAATGGCAAAGAGAATGCCAACTGGTGCTGT... | AATGAATACTAAGCTAGTGAAAAAACTTATTTAAAGACCTAAACGAAGCATATGTGGACAGAAAGGAGATGACTAAAAATTGCCAATGACATAAAACTATCCACTGTAAAGGCTGAAAGTCTTTGCTAAGTTATGATGAAATTCCCTCTTCACAAAGTAAAAGCAATACTTAATGTATAATGATAGGATCAAAGTTAATAGTTTAAAAAACAAAATAGATTGGTAAGATTTGCCAGAGTGAGAAAAACGATAGAACAATAGAAGACATGATAAAGATTGATAAAATAATGAATGGCAAAGAGAATGCCAACTGGTGCTGT... |
Task1_train_45509 | Mutation context: Chromosome 17. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GATCTGAAATATTTCAGATGTGACTATGAAGGAACAAAGACAAATTCTGTGTTCTACAAATATATTTAAAACATAATGGGGCCAGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGCGGATCACCTTAGGTCAGGAGTTCAACACCAGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAAAATAGCCAGCCTGGGGGGACACACCTGTAATCCTGGTTACTCAGGAGGCTGAGGCAGAAGGATTCCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCCAAGATTGCGCTACTG... | GATCTGAAATATTTCAGATGTGACTATGAAGGAACAAAGACAAATTCTGTGTTCTACAAATATATTTAAAACATAATGGGGCCAGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGCGGATCACCTTAGGTCAGGAGTTCAACACCAGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAAAATAGCCAGCCTGGGGGGACACACCTGTAATCCTGGTTACTCAGGAGGCTGAGGCAGAAGGATTCCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCCAAGATTGCGCTACTG... |
Task1_train_45510 | A mutation on Chromosome 17 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | ATGGGTCCAGTAATATTTTGGCCAGGGCTACGATCTGCGGTGTGCGGTCCCAGCCATCTGAGCAGTGTACCAGCACAGGCCGGCCTTCCCGGTCTACTGTATTAGCCACCAGCACAGCTGCTTTTAGCATCACCGACAAGTGCTGCAGCCATTTGGTACTCTCCAGTGCCGACAACCAGCTACACAAAAGCAGACATCAAGTCGGTCACAAAGGGTGCTGAGGCCACAGCAGTCTCTCCACCATCCACAGCCAGCCCCACCCAACAAAGTCCCCATTGAGAACTGAAACCAAGAGGTACAACCCAGGGCCTTTTGGACAA... | ATGGGTCCAGTAATATTTTGGCCAGGGCTACGATCTGCGGTGTGCGGTCCCAGCCATCTGAGCAGTGTACCAGCACAGGCCGGCCTTCCCGGTCTACTGTATTAGCCACCAGCACAGCTGCTTTTAGCATCACCGACAAGTGCTGCAGCCATTTGGTACTCTCCAGTGCCGACAACCAGCTACACAAAAGCAGACATCAAGTCGGTCACAAAGGGTGCTGAGGCCACAGCAGTCTCTCCACCATCCACAGCCAGCCCCACCCAACAAAGTCCCCATTGAGAACTGAAACCAAGAGGTACAACCCAGGGCCTTTTGGACAA... |
Task1_train_45511 | A change on Chromosome 17 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GGGCAGGGGGGACTTTTGGACAGTCCTTTAATATTGGGGAAGTGCCCCAAATTTCTTTTTCTTTTTATTTTTCTTTTTTTTTTTTGAGACGGAGTCTCGCCCTGTCACCCAGGCTGGAGTGCAGTGGCGCCATCTCAGCTCACTTCAAGCTCCGCCTCCCGGGTTCAGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCGCCACCACGCCCGGCTATTTTGTATTTTTAGTAGAGACAGGGTTTCACTTTCTCCTTAGCCAGGAGAAGTGCCCCAAATTTCTAATCCCTTAAGCCAGGACCTTG... | GGGCAGGGGGGACTTTTGGACAGTCCTTTAATATTGGGGAAGTGCCCCAAATTTCTTTTTCTTTTTATTTTTCTTTTTTTTTTTTGAGACGGAGTCTCGCCCTGTCACCCAGGCTGGAGTGCAGTGGCGCCATCTCAGCTCACTTCAAGCTCCGCCTCCCGGGTTCAGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCGCCACCACGCCCGGCTATTTTGTATTTTTAGTAGAGACAGGGTTTCACTTTCTCCTTAGCCAGGAGAAGTGCCCCAAATTTCTAATCCCTTAAGCCAGGACCTTG... |
Task1_train_45512 | This mutation is located on Chromosome 17. Is it associated with a disease or is it a benign polymorphism? | Benign | GCTAGTTCTGATCCCCAAAAAAAACCCATCAGGAATGCTTCCCTTAGTCCAGCATAACCTCCTCTGGGGAGACTCCTGCCCCTAATGTCCCAATCCAAGGATGAGAAGCATCTGTCCACCCCATTCCTTAGACAAAAGGGCTTTGAGGGGCCATTTGGGAAGGGACTGACACTTAAAGAGATGGGCTGAATCAGGCCCCATCCCCAGCTGTTCACCCAGAGAGGCTTGTGAAGCTCAACAACAAACATGATGCCTTCCACAAGCCAGGCATCGTGGCCAGGCCACCAGAGAATTCCTGCCAGGAATGGAATCTGGAACAG... | GCTAGTTCTGATCCCCAAAAAAAACCCATCAGGAATGCTTCCCTTAGTCCAGCATAACCTCCTCTGGGGAGACTCCTGCCCCTAATGTCCCAATCCAAGGATGAGAAGCATCTGTCCACCCCATTCCTTAGACAAAAGGGCTTTGAGGGGCCATTTGGGAAGGGACTGACACTTAAAGAGATGGGCTGAATCAGGCCCCATCCCCAGCTGTTCACCCAGAGAGGCTTGTGAAGCTCAACAACAAACATGATGCCTTCCACAAGCCAGGCATCGTGGCCAGGCCACCAGAGAATTCCTGCCAGGAATGGAATCTGGAACAG... |
Task1_train_45513 | A variant found on Chromosome 17 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | ATTTACTAAAGATGCCCAGTGGACTTGGGCAAACCTGGCCCAATCCCTTCCTAGTGCAAGTGGCCCAAACAACAGCAGCTAGTATTTACTGAGTGCTCACTGTTGCCAAGCACCGTGCTAAGTGTTTTATTGGTAATAACTTGTAATAATCCTCACAATAACCCTAAGAGGGAGCCATTATTCTCAGTAACAGATGAGGAAACTGAGGCTTGGAGAGGTAAAATAACTTACCCAAGGTCACAGTCAGAAAATAGTGGACCCAGGGCCCAAATCCAGTTAGATAACTCGAGTTCGTACTTTACTATGCCCCTACTTTATAG... | ATTTACTAAAGATGCCCAGTGGACTTGGGCAAACCTGGCCCAATCCCTTCCTAGTGCAAGTGGCCCAAACAACAGCAGCTAGTATTTACTGAGTGCTCACTGTTGCCAAGCACCGTGCTAAGTGTTTTATTGGTAATAACTTGTAATAATCCTCACAATAACCCTAAGAGGGAGCCATTATTCTCAGTAACAGATGAGGAAACTGAGGCTTGGAGAGGTAAAATAACTTACCCAAGGTCACAGTCAGAAAATAGTGGACCCAGGGCCCAAATCCAGTTAGATAACTCGAGTTCGTACTTTACTATGCCCCTACTTTATAG... |
Task1_train_45514 | A change on Chromosome 17 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GAAGCCTCACTAAGATTCAGTATTGTACAATGAAAGAACAACAGACCAGGAGTCAGGAGACCTGCCCCTAACCAACTTGGCCCTTGGTTGTAGCACAGCAAGTTGAGAGGTGGCAGGGAGAGCTATCTTCCCTGTATAGGCAATAAAAGGGTGATATGGCCAGGCACGGTGGCTCATGCCTGTAATCCTAGCACTTTGGGAGGCTGAGGCAGGTGGATCACCTATGGTCAGGAGTTCAAGACCAGCTGGGCCAACATGGTGAAAACCTGTCTCTACTAAAAATACAAAAAATTAGCCAGGCATGGTGGCACGTGACTGTA... | GAAGCCTCACTAAGATTCAGTATTGTACAATGAAAGAACAACAGACCAGGAGTCAGGAGACCTGCCCCTAACCAACTTGGCCCTTGGTTGTAGCACAGCAAGTTGAGAGGTGGCAGGGAGAGCTATCTTCCCTGTATAGGCAATAAAAGGGTGATATGGCCAGGCACGGTGGCTCATGCCTGTAATCCTAGCACTTTGGGAGGCTGAGGCAGGTGGATCACCTATGGTCAGGAGTTCAAGACCAGCTGGGCCAACATGGTGAAAACCTGTCTCTACTAAAAATACAAAAAATTAGCCAGGCATGGTGGCACGTGACTGTA... |
Task1_train_45515 | With a mutation on Chromosome 17, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | ATCTTGCTGCTGCACTCCAGTCTGGATGACAGAGTGAGACCTTGTCTCTTAAAAAAAAGAAAAAAGAAAAAAAAAGGAAAAGAATCAGTACGGTTTTGGTCAGGCTGAAGACTCTGTGCTCTCTATATGTAAAGACAGTATAATTAAATAACCAGAAAAAGGCTTCTAGGGTATGAAAGCACAAACTGAAGCTAAAAATATCAAAAGGTAAGTGAACCAGATTTTCAATGCCATTGGGAAAAATCAGACCTAACACTTCTATGGATTTTATGCATAATTAGGGAATTCTTAAAAAAAAAAAAAAAAAAAGAGGGACCTAT... | ATCTTGCTGCTGCACTCCAGTCTGGATGACAGAGTGAGACCTTGTCTCTTAAAAAAAAGAAAAAAGAAAAAAAAAGGAAAAGAATCAGTACGGTTTTGGTCAGGCTGAAGACTCTGTGCTCTCTATATGTAAAGACAGTATAATTAAATAACCAGAAAAAGGCTTCTAGGGTATGAAAGCACAAACTGAAGCTAAAAATATCAAAAGGTAAGTGAACCAGATTTTCAATGCCATTGGGAAAAATCAGACCTAACACTTCTATGGATTTTATGCATAATTAGGGAATTCTTAAAAAAAAAAAAAAAAAAAGAGGGACCTAT... |
Task1_train_45516 | This mutation is located on Chromosome 17. Is it associated with a disease or is it a benign polymorphism? | Benign | GAACCCGGGAGGCCAAGGTTGCAGTGAGCCGAGATCACACCACTGCACTCCAGCCTGGGTGATAGAGTGAATAAAAAAAAAAAGGAATTCCATAGACCCTGTTACAAGGATACTCCCTTAACTGCTCTGCAGATAACAGCTCGAACATTATGAAGCATTGCGTTTTCTCTTTAAATATTATTTCAGATCCTACATACCACTCAAACTACAGATGGCAGTTGGTCTAAAGAACCCTTCAAAAACCTGATTCACCAAAGAATGCAGTTTCCACATCCTCATAATTTCATCCCCCGACTCTGACCAATCAATGGCCCCAGTTT... | GAACCCGGGAGGCCAAGGTTGCAGTGAGCCGAGATCACACCACTGCACTCCAGCCTGGGTGATAGAGTGAATAAAAAAAAAAAGGAATTCCATAGACCCTGTTACAAGGATACTCCCTTAACTGCTCTGCAGATAACAGCTCGAACATTATGAAGCATTGCGTTTTCTCTTTAAATATTATTTCAGATCCTACATACCACTCAAACTACAGATGGCAGTTGGTCTAAAGAACCCTTCAAAAACCTGATTCACCAAAGAATGCAGTTTCCACATCCTCATAATTTCATCCCCCGACTCTGACCAATCAATGGCCCCAGTTT... |
Task1_train_45517 | A mutation on Chromosome 17 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | ATTGCTATGGCAATGGTAAACTGACATAGCATTGGTAGGTGTGTCTTAGGGAGAGGTGCTTTCACCCCTTCCCTGTTTCAGCTAGTCTTTTTTTTTTGATATGGAGTCTCACTCTGTCATCCAAGCTGGAGTGTCGTGGCGCGATCTTGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGTGATTCTCCTGCCACAGCCTCCCAGGTAGCTGGGATTACAGGTGCACACCACTGTGCCTAATTTTTGTATTTTTAGTAGAAACGAGGTTTCACTATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCTGC... | ATTGCTATGGCAATGGTAAACTGACATAGCATTGGTAGGTGTGTCTTAGGGAGAGGTGCTTTCACCCCTTCCCTGTTTCAGCTAGTCTTTTTTTTTTGATATGGAGTCTCACTCTGTCATCCAAGCTGGAGTGTCGTGGCGCGATCTTGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGTGATTCTCCTGCCACAGCCTCCCAGGTAGCTGGGATTACAGGTGCACACCACTGTGCCTAATTTTTGTATTTTTAGTAGAAACGAGGTTTCACTATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCTGC... |
Task1_train_45518 | Here’s a variant located on Chromosome 17. What is the predicted biological effect — harmless or disease-causing? | Benign | GGTGTGTCTTAGGGAGAGGTGCTTTCACCCCTTCCCTGTTTCAGCTAGTCTTTTTTTTTTGATATGGAGTCTCACTCTGTCATCCAAGCTGGAGTGTCGTGGCGCGATCTTGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGTGATTCTCCTGCCACAGCCTCCCAGGTAGCTGGGATTACAGGTGCACACCACTGTGCCTAATTTTTGTATTTTTAGTAGAAACGAGGTTTCACTATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCTGCCCGCCTCAGCTCCCAAAGCATTGGGATTACAGGAGTG... | GGTGTGTCTTAGGGAGAGGTGCTTTCACCCCTTCCCTGTTTCAGCTAGTCTTTTTTTTTTGATATGGAGTCTCACTCTGTCATCCAAGCTGGAGTGTCGTGGCGCGATCTTGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGTGATTCTCCTGCCACAGCCTCCCAGGTAGCTGGGATTACAGGTGCACACCACTGTGCCTAATTTTTGTATTTTTAGTAGAAACGAGGTTTCACTATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCTGCCCGCCTCAGCTCCCAAAGCATTGGGATTACAGGAGTG... |
Task1_train_45519 | A mutation located on Chromosome 17 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TGGCAGCTTGCCTCCATGTCCCCACAGTCTTTTCTCTCCCACATCTGTGATTCCTACCCCATCCTTTTGGTTAGGCAAGTGTGACCGGCAGGCAGACCTTAGCATTTCTCAACAAATGCGGTGCTGGGACTCTAAAGTTCAGGTCCCCCTCTTCTCAACACTCTCCTTAACACGGAGGCTCCATGGCAGGTGACATTCTGCGCCTCGGATGCGCCGGAGAGGTCCTTGCTGGCCGACCGGGAAGACAGTCTGCCCAAGCTCTGCCATGCATGGGGGCTGCACAGCAACATCAGCGGCATGAAGGAGCGGCTGTCCAACAT... | TGGCAGCTTGCCTCCATGTCCCCACAGTCTTTTCTCTCCCACATCTGTGATTCCTACCCCATCCTTTTGGTTAGGCAAGTGTGACCGGCAGGCAGACCTTAGCATTTCTCAACAAATGCGGTGCTGGGACTCTAAAGTTCAGGTCCCCCTCTTCTCAACACTCTCCTTAACACGGAGGCTCCATGGCAGGTGACATTCTGCGCCTCGGATGCGCCGGAGAGGTCCTTGCTGGCCGACCGGGAAGACAGTCTGCCCAAGCTCTGCCATGCATGGGGGCTGCACAGCAACATCAGCGGCATGAAGGAGCGGCTGTCCAACAT... |
Task1_train_45520 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | TGAGGATAGAGCTGAGTAACTTAAAAATGTTAGTCCTTGGTCACAAAGACTATTTGGTAATTAATAAAGAAGTGCCTCTTGACATTAGACTGCAATTAACTGAGGGGTGGGGGGCAGCTTCATAAACTGCAAGTACGTCAATTTACTCTTTCCAAAATTTAAAAAGAAAATAATTCGATTTGAGGAGTAAACTCAGGTTTCTAAATCACACAGTTACCATCTTAGGGTGTGGGTTTGCTTCATCTCTTTCAGTACATCCCCCAACCAACCCCCTCCTAGGGAACTTAAATGCAATGGCTCAAAACTAATAGGACTGCAAA... | TGAGGATAGAGCTGAGTAACTTAAAAATGTTAGTCCTTGGTCACAAAGACTATTTGGTAATTAATAAAGAAGTGCCTCTTGACATTAGACTGCAATTAACTGAGGGGTGGGGGGCAGCTTCATAAACTGCAAGTACGTCAATTTACTCTTTCCAAAATTTAAAAAGAAAATAATTCGATTTGAGGAGTAAACTCAGGTTTCTAAATCACACAGTTACCATCTTAGGGTGTGGGTTTGCTTCATCTCTTTCAGTACATCCCCCAACCAACCCCCTCCTAGGGAACTTAAATGCAATGGCTCAAAACTAATAGGACTGCAAA... |
Task1_train_45521 | This alteration on Chromosome 17 may affect genome function. Does it lead to a disease or is it benign? | Benign | TTCCCGACCTCAGGTGATCTGCCTGTCTCCGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACGCCCGGCCAATTTTTGTATTTTTTGTAGAGATGGGGTTTCGCCATGTTGCCCAGGCTGGTCTCAGACTCCTGGGCTCAAGCGGTATGCCCACCTTGGCCTCCCAAAGTGCCGGGATTACTCAGTCTATACGTGGATTTTGACTGCATTGGGGGATGGGGGGTACTTAGCACCCCTACCCTCCACATTGTTCAAGGGTCAAGTGTACTTTTCCCCTTCCAATCTTTACATCATTTATTTTTCTTTCCTAATT... | TTCCCGACCTCAGGTGATCTGCCTGTCTCCGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACGCCCGGCCAATTTTTGTATTTTTTGTAGAGATGGGGTTTCGCCATGTTGCCCAGGCTGGTCTCAGACTCCTGGGCTCAAGCGGTATGCCCACCTTGGCCTCCCAAAGTGCCGGGATTACTCAGTCTATACGTGGATTTTGACTGCATTGGGGGATGGGGGGTACTTAGCACCCCTACCCTCCACATTGTTCAAGGGTCAAGTGTACTTTTCCCCTTCCAATCTTTACATCATTTATTTTTCTTTCCTAATT... |
Task1_train_45522 | Given this context: Chromosome 17 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TGTGAGCCACCACGCCCGGCCAATTTTTGTATTTTTTGTAGAGATGGGGTTTCGCCATGTTGCCCAGGCTGGTCTCAGACTCCTGGGCTCAAGCGGTATGCCCACCTTGGCCTCCCAAAGTGCCGGGATTACTCAGTCTATACGTGGATTTTGACTGCATTGGGGGATGGGGGGTACTTAGCACCCCTACCCTCCACATTGTTCAAGGGTCAAGTGTACTTTTCCCCTTCCAATCTTTACATCATTTATTTTTCTTTCCTAATTGCACTGTCTAGGGCCTCTAGTACAGTGTTGAATATAAGTTTTAAGTTTAGGCATCT... | TGTGAGCCACCACGCCCGGCCAATTTTTGTATTTTTTGTAGAGATGGGGTTTCGCCATGTTGCCCAGGCTGGTCTCAGACTCCTGGGCTCAAGCGGTATGCCCACCTTGGCCTCCCAAAGTGCCGGGATTACTCAGTCTATACGTGGATTTTGACTGCATTGGGGGATGGGGGGTACTTAGCACCCCTACCCTCCACATTGTTCAAGGGTCAAGTGTACTTTTCCCCTTCCAATCTTTACATCATTTATTTTTCTTTCCTAATTGCACTGTCTAGGGCCTCTAGTACAGTGTTGAATATAAGTTTTAAGTTTAGGCATCT... |
Task1_train_45523 | A mutation is present on Chromosome 17. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GTGCTGGCGGCGGCCGAGCGCGCCCAAGCTCGAGGTCCGAGAGGACCGCGAGGACGGCCGCCCCGGGCCAGCCGGGCGTGGAAAAAAGGAAATTGCTGGGAAGGGGGCAAGCTGTCCCGAGGTCTGGATGTGGCTTCGTGGCGGAGAGAAAAGGAAGAGGCAAACCCTGAGCCCGGGAGGGAGAGCACTGAGCAGGCCTCGTCCCCAGTCCGAGCTGCGGGACCGGCGTCAGTGGACGCGGGCGGTGAACCAGCTCCTCACAGGGCAGGGCTGAGCGCGTAGGACTGAGAGCGCAGGGCGCGAGCCGCAGGGCTCCGCTG... | GTGCTGGCGGCGGCCGAGCGCGCCCAAGCTCGAGGTCCGAGAGGACCGCGAGGACGGCCGCCCCGGGCCAGCCGGGCGTGGAAAAAAGGAAATTGCTGGGAAGGGGGCAAGCTGTCCCGAGGTCTGGATGTGGCTTCGTGGCGGAGAGAAAAGGAAGAGGCAAACCCTGAGCCCGGGAGGGAGAGCACTGAGCAGGCCTCGTCCCCAGTCCGAGCTGCGGGACCGGCGTCAGTGGACGCGGGCGGTGAACCAGCTCCTCACAGGGCAGGGCTGAGCGCGTAGGACTGAGAGCGCAGGGCGCGAGCCGCAGGGCTCCGCTG... |
Task1_train_45524 | A genomic variant on Chromosome 17 is under review. What is the biological outcome — benign or pathogenic? | Benign | CAAATGTGGAAACTGAGGCACAGAGAAGCCCAGTGACTTGTCTGAGATCAAACAGTGACTCGGTGGCACCCTGGACTTTTGCTGACAGCTCACAATTCCACCTGCTACACTGTGCTGAGTTCACAGTGGGCTTTGACAGTGTTAAGGGCTGACTCAAGTTCTCCATTACCACAGTGAATCAACTGGTCACATCAAGGAGGGCCTGGAGCTGGGCATTAGTGCTGGTGCAGAGAGGCTAAGTAGGGCTGGGGTGGGGAGAGTTTGGGGCCCAGGGGCCTGGTTCTTCACTTGGGAGCTCCAGTCCTGGTCGGTAGGCCCCG... | CAAATGTGGAAACTGAGGCACAGAGAAGCCCAGTGACTTGTCTGAGATCAAACAGTGACTCGGTGGCACCCTGGACTTTTGCTGACAGCTCACAATTCCACCTGCTACACTGTGCTGAGTTCACAGTGGGCTTTGACAGTGTTAAGGGCTGACTCAAGTTCTCCATTACCACAGTGAATCAACTGGTCACATCAAGGAGGGCCTGGAGCTGGGCATTAGTGCTGGTGCAGAGAGGCTAAGTAGGGCTGGGGTGGGGAGAGTTTGGGGCCCAGGGGCCTGGTTCTTCACTTGGGAGCTCCAGTCCTGGTCGGTAGGCCCCG... |
Task1_train_45525 | This alteration occurs on Chromosome 17. Is it associated with a disease or is it a benign variant? | Benign | TGGTGACCTGTGGTCAAATTATGATGATCAATAATTTGCATATTGTTGTAAGTATTCACAACAATGAAGATGATAAGTAACAATTACTTCTAATTTATGGTCTCTACTATATTATGCTTTTGCTGAAGCTTGAAGAAAGCTCATATGTACATAGACGGTGTGTCTAAAAGAAACACGATTTTTAAAAAATGTCTGACTGTATACATCAAATGAGCAATACCTCCTACAAAGGAGCTCCCTTGGGAAGCTATACAAACATTGTTAACAATCCTGCATTAGATCAAAACACTTTTGGAACTTCTTTATTGGAATTGCCTTAT... | TGGTGACCTGTGGTCAAATTATGATGATCAATAATTTGCATATTGTTGTAAGTATTCACAACAATGAAGATGATAAGTAACAATTACTTCTAATTTATGGTCTCTACTATATTATGCTTTTGCTGAAGCTTGAAGAAAGCTCATATGTACATAGACGGTGTGTCTAAAAGAAACACGATTTTTAAAAAATGTCTGACTGTATACATCAAATGAGCAATACCTCCTACAAAGGAGCTCCCTTGGGAAGCTATACAAACATTGTTAACAATCCTGCATTAGATCAAAACACTTTTGGAACTTCTTTATTGGAATTGCCTTAT... |
Task1_train_45526 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | TGAGCCATATAGAAAACTCAGTCTCATTAATTTATAGTCACACATAATTAATTTTTCACCTCTGGTGGAGTTACCCAGCTTGATCACCCATTTTGGCTCTGAATGATTTTGCTGCTTCCAAAATAAAATCCAATCTCAAAGTGTGAGTATTTGCCACTATCTAGAGTGTTTAGGAGAACATATCACATGTTATGAAGGCAATTCCAAAAAGAACTCCAGAATTTCAGATTCTGGAATAACATATCTCATGGCAGTGAGTTTGCTGAGGGCAACTCTCCTCTGCACAGCAAGTTGTATTTAATAGTATATTTGATTTTAAA... | TGAGCCATATAGAAAACTCAGTCTCATTAATTTATAGTCACACATAATTAATTTTTCACCTCTGGTGGAGTTACCCAGCTTGATCACCCATTTTGGCTCTGAATGATTTTGCTGCTTCCAAAATAAAATCCAATCTCAAAGTGTGAGTATTTGCCACTATCTAGAGTGTTTAGGAGAACATATCACATGTTATGAAGGCAATTCCAAAAAGAACTCCAGAATTTCAGATTCTGGAATAACATATCTCATGGCAGTGAGTTTGCTGAGGGCAACTCTCCTCTGCACAGCAAGTTGTATTTAATAGTATATTTGATTTTAAA... |
Task1_train_45527 | A mutation located on Chromosome 17 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GAAACGGGGAGGACTAGAGGCACTATTCTCTGATGACCCGAGCTCAGGTGTTGCCTTCGGTATTTTACCAGTAAAATACTGTCCCAAAGAATTAAAGCTTGACCAGCTAACTCTCTTTGTTTGTTTGTTGAAAGTTGGGCTTGTGGATCTGGAAATCACAATTTTTTCTGCTTTCCCTGCTTCTTCCAGGAATACTGGATCATCTAAGAATACAAGAATTTAAGAGATTTAACTTTCTGCTCCTAGCTAACATAATTGCTAGGTTAAAATAATTATTTATTAGAAATACCTAAATAACTGTATAGGATACATAACTTAGA... | GAAACGGGGAGGACTAGAGGCACTATTCTCTGATGACCCGAGCTCAGGTGTTGCCTTCGGTATTTTACCAGTAAAATACTGTCCCAAAGAATTAAAGCTTGACCAGCTAACTCTCTTTGTTTGTTTGTTGAAAGTTGGGCTTGTGGATCTGGAAATCACAATTTTTTCTGCTTTCCCTGCTTCTTCCAGGAATACTGGATCATCTAAGAATACAAGAATTTAAGAGATTTAACTTTCTGCTCCTAGCTAACATAATTGCTAGGTTAAAATAATTATTTATTAGAAATACCTAAATAACTGTATAGGATACATAACTTAGA... |
Task1_train_45528 | Here’s a variant located on Chromosome 17. What is the predicted biological effect — harmless or disease-causing? | Benign | TGTTTCTCATGTTTACCCATTGTAATAACACCATTTCTTTCTCTATAATCAAATGGATTCAAATGTTAAGTGTTATGATTCATCCTGCTATTCACCTATGCAGCTATACTCACTGTTATTTCTGGGACATTCATTTGTGTTATTCCAGAAATATCAAACTAATTAAGGTAGTTAACCAACAGTCACAGTGAGTAGTGTACTCAGAGATTCATGGTGAAAGAATCTTACGTCCTGAGGCCTCTAGCCCTGGGACACCAGCTGCACCAGGGCTAAGAAGCTTGAGAAGATCAATAGTTTGATATTAATACATTGGAAATCTT... | TGTTTCTCATGTTTACCCATTGTAATAACACCATTTCTTTCTCTATAATCAAATGGATTCAAATGTTAAGTGTTATGATTCATCCTGCTATTCACCTATGCAGCTATACTCACTGTTATTTCTGGGACATTCATTTGTGTTATTCCAGAAATATCAAACTAATTAAGGTAGTTAACCAACAGTCACAGTGAGTAGTGTACTCAGAGATTCATGGTGAAAGAATCTTACGTCCTGAGGCCTCTAGCCCTGGGACACCAGCTGCACCAGGGCTAAGAAGCTTGAGAAGATCAATAGTTTGATATTAATACATTGGAAATCTT... |
Task1_train_45529 | A variant affecting Chromosome 17 has been observed. Determine if it's benign or associated with disease. | Benign | TTACATGTATTATCTCATTTCATCGTTACCAGAGTCTTAAGATGAGGAAACGGCATAGAGAGATGAAGCACTTTGCCCAAGTCCCATATTCAGTGGCAGACCTAGAATCGAAGCACTAGCTGCCGGGCACGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGACCAAGGTGGGCGGATCACCCGAGGTTGGGAGTTTGAGACCACCCTGACCAACATGGAGAAATCTCATCTCTACTAAAAATACAAAAAAATTAGCCAGGTGTGGTGGTGCATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGAATTGCTT... | TTACATGTATTATCTCATTTCATCGTTACCAGAGTCTTAAGATGAGGAAACGGCATAGAGAGATGAAGCACTTTGCCCAAGTCCCATATTCAGTGGCAGACCTAGAATCGAAGCACTAGCTGCCGGGCACGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGACCAAGGTGGGCGGATCACCCGAGGTTGGGAGTTTGAGACCACCCTGACCAACATGGAGAAATCTCATCTCTACTAAAAATACAAAAAAATTAGCCAGGTGTGGTGGTGCATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGAATTGCTT... |
Task1_train_45530 | Located on Chromosome 17, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | GGTGATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGTGCCTGGCCAACACCCTTTATTTTCCATCACACTGCCTCTGAGCAGAAAATCATTAGATATTCATTTTCCTAAGAAAGAGTCTTCACTTGATGAGAGATTTCCTACCCAGGGCTTTTGTTTGTTTGTTTGTTTGGAAACCTTATAGAGCTAATGAAAGTGGGAAAAGAGAAATGTAAAATTACAGAGTTAGAAGCTGCTGCTAATAGATCATTCAACAATAGAGATAAAAGTGTCCTAGGGCTGGGCGCGGTGAAACCCCGTCT... | GGTGATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGTGCCTGGCCAACACCCTTTATTTTCCATCACACTGCCTCTGAGCAGAAAATCATTAGATATTCATTTTCCTAAGAAAGAGTCTTCACTTGATGAGAGATTTCCTACCCAGGGCTTTTGTTTGTTTGTTTGTTTGGAAACCTTATAGAGCTAATGAAAGTGGGAAAAGAGAAATGTAAAATTACAGAGTTAGAAGCTGCTGCTAATAGATCATTCAACAATAGAGATAAAAGTGTCCTAGGGCTGGGCGCGGTGAAACCCCGTCT... |
Task1_train_45531 | This sequence variant lies on Chromosome 17. Is it clinically significant, and what condition might it cause if any? | Benign | AAGTGGGAAAAGAGAAATGTAAAATTACAGAGTTAGAAGCTGCTGCTAATAGATCATTCAACAATAGAGATAAAAGTGTCCTAGGGCTGGGCGCGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCTGGGCATGGTGGTGGGCGCCTGCAGTCCCAGCTACTGGGGAGGCTGAGGCAGGAGAATGGTGTGAACCCTGGAGGTGGAGCTTGCAGTGAGCCGAGATGGCGCCACTGCACTCCAGCCTGGGAGACAGAGCGAGACTCTGTCTTGAAAAAAAAAAAAGTGTCCTAGAGATGATCATGTAAGTTCAAA... | AAGTGGGAAAAGAGAAATGTAAAATTACAGAGTTAGAAGCTGCTGCTAATAGATCATTCAACAATAGAGATAAAAGTGTCCTAGGGCTGGGCGCGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCTGGGCATGGTGGTGGGCGCCTGCAGTCCCAGCTACTGGGGAGGCTGAGGCAGGAGAATGGTGTGAACCCTGGAGGTGGAGCTTGCAGTGAGCCGAGATGGCGCCACTGCACTCCAGCCTGGGAGACAGAGCGAGACTCTGTCTTGAAAAAAAAAAAAGTGTCCTAGAGATGATCATGTAAGTTCAAA... |
Task1_train_45532 | A mutation on Chromosome 17 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GTTGGGCATGGTGGCACGCACCTGTAATCCCAGCTACTACGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCGAGATCACACCACTGCACTCCAGCCTCCAGGCCGGGCGACAGTGCAAGGCTCCATCTCAAAAACAAACAAACAAACAAACAAACAAACAAAAAAGAGATTCTAACATTCAGCCAGGCATGGTGGCTCATGTCTGTAATCCTAACACTTTGGGAGGCCGAGGCAGGAAGATCACTTGAGCCCAGGAGTTTGAGACCAGCCTGGGCAACAAAGTGAGACTCCTGTCT... | GTTGGGCATGGTGGCACGCACCTGTAATCCCAGCTACTACGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCGAGATCACACCACTGCACTCCAGCCTCCAGGCCGGGCGACAGTGCAAGGCTCCATCTCAAAAACAAACAAACAAACAAACAAACAAACAAAAAAGAGATTCTAACATTCAGCCAGGCATGGTGGCTCATGTCTGTAATCCTAACACTTTGGGAGGCCGAGGCAGGAAGATCACTTGAGCCCAGGAGTTTGAGACCAGCCTGGGCAACAAAGTGAGACTCCTGTCT... |
Task1_train_45533 | A variant on Chromosome 17 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | AGCCGGCCCAGAAGTGCACCCATGTCCTCTGGTATCCACTGGCTCTCCAAGCCAAACTGGGCAGGGAGGAGTTGTGAGGGAAAACTGCAGGTCAGGAGGGAGGCTGGCAAAGCGGGCCAGGGCCAGGCCTGACCCCAGCTCTCCTCTCCCGGCCCCACTGCCGGCCAGTGTTTAACAAGGCCCTGCCTTCTCCCTCTAGTGCTAGGGACAGCCACCTTCTTCCTCTCCCCACCGCCCCCTCTCCCCTGCAACACGTCATCTGACAAGTCAGTGCGATCTCACTGGAGGTGCATCTCACAGGAACGCGGGGTCACAGCCTC... | AGCCGGCCCAGAAGTGCACCCATGTCCTCTGGTATCCACTGGCTCTCCAAGCCAAACTGGGCAGGGAGGAGTTGTGAGGGAAAACTGCAGGTCAGGAGGGAGGCTGGCAAAGCGGGCCAGGGCCAGGCCTGACCCCAGCTCTCCTCTCCCGGCCCCACTGCCGGCCAGTGTTTAACAAGGCCCTGCCTTCTCCCTCTAGTGCTAGGGACAGCCACCTTCTTCCTCTCCCCACCGCCCCCTCTCCCCTGCAACACGTCATCTGACAAGTCAGTGCGATCTCACTGGAGGTGCATCTCACAGGAACGCGGGGTCACAGCCTC... |
Task1_train_45534 | Here is a genetic alteration on Chromosome 17. Based on the data, is it a benign variant or a cause of disease? | Benign | GTCTCCCGCAGGGATCTCCCCAGGGCCCGGGCTCTGGAAGCCCTTGGCCTTCCTCCCCTCCCCCAGCACCGTGGCTTCTCCTTTATGGCCTGCATCTAAGCAGGGTCCTACACCCTCCCTGCCCTCCTGGTGCCCAATAGGAGGAAGCAGCCCTGCTCAGCCAGGAGTTTGCGGAGGCCTGGGGCCAGAAGGCCAAGGAGCTGTATGAACCGATCTGGCAGAACTTCACGGACCCGCAGCTGCGCAGGATCATCGGAGCTGTGCGCACCCTGGGCTCTGCCAACCTGCCCCTGGCTAAGCGGCAGCAGGTGGGCTGAGGG... | GTCTCCCGCAGGGATCTCCCCAGGGCCCGGGCTCTGGAAGCCCTTGGCCTTCCTCCCCTCCCCCAGCACCGTGGCTTCTCCTTTATGGCCTGCATCTAAGCAGGGTCCTACACCCTCCCTGCCCTCCTGGTGCCCAATAGGAGGAAGCAGCCCTGCTCAGCCAGGAGTTTGCGGAGGCCTGGGGCCAGAAGGCCAAGGAGCTGTATGAACCGATCTGGCAGAACTTCACGGACCCGCAGCTGCGCAGGATCATCGGAGCTGTGCGCACCCTGGGCTCTGCCAACCTGCCCCTGGCTAAGCGGCAGCAGGTGGGCTGAGGG... |
Task1_train_45535 | Located on Chromosome 17, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | ATACCTTCTCTGCATCTCCCTGGCCTCACTTTCTGCTGCCCCGCCAGCCCACACTCTTAGGGGACCCTCTTCTCCCTCTGACCTCTTCCCTCTCCTTTCATCTCATCTCCCAACAGAAAGTGACATCAATTACTTGCTAAAAATGGCACTGGAAAAAATTGCCTTCCTGCCCTTTGGCTACTTGGTGGACCAGTGGCGCTGGGGGGTCTTTAGTGGGCGTACCCCCCCTTCCCGCTACAACTTCGACTGGTGGTATCTTCGGTGAGAGGAGGGATAGAAAAGCCTTCGCCCCAGCTAGCCCTCCCCAGCCTCCTGGACAG... | ATACCTTCTCTGCATCTCCCTGGCCTCACTTTCTGCTGCCCCGCCAGCCCACACTCTTAGGGGACCCTCTTCTCCCTCTGACCTCTTCCCTCTCCTTTCATCTCATCTCCCAACAGAAAGTGACATCAATTACTTGCTAAAAATGGCACTGGAAAAAATTGCCTTCCTGCCCTTTGGCTACTTGGTGGACCAGTGGCGCTGGGGGGTCTTTAGTGGGCGTACCCCCCCTTCCCGCTACAACTTCGACTGGTGGTATCTTCGGTGAGAGGAGGGATAGAAAAGCCTTCGCCCCAGCTAGCCCTCCCCAGCCTCCTGGACAG... |
Task1_train_45536 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | CACTCTTAGGGGACCCTCTTCTCCCTCTGACCTCTTCCCTCTCCTTTCATCTCATCTCCCAACAGAAAGTGACATCAATTACTTGCTAAAAATGGCACTGGAAAAAATTGCCTTCCTGCCCTTTGGCTACTTGGTGGACCAGTGGCGCTGGGGGGTCTTTAGTGGGCGTACCCCCCCTTCCCGCTACAACTTCGACTGGTGGTATCTTCGGTGAGAGGAGGGATAGAAAAGCCTTCGCCCCAGCTAGCCCTCCCCAGCCTCCTGGACAGCCAGGCGCCTCCTGCCCCAGCCAGTTCTAGCCTCTCCTCTCTAATGATGTC... | CACTCTTAGGGGACCCTCTTCTCCCTCTGACCTCTTCCCTCTCCTTTCATCTCATCTCCCAACAGAAAGTGACATCAATTACTTGCTAAAAATGGCACTGGAAAAAATTGCCTTCCTGCCCTTTGGCTACTTGGTGGACCAGTGGCGCTGGGGGGTCTTTAGTGGGCGTACCCCCCCTTCCCGCTACAACTTCGACTGGTGGTATCTTCGGTGAGAGGAGGGATAGAAAAGCCTTCGCCCCAGCTAGCCCTCCCCAGCCTCCTGGACAGCCAGGCGCCTCCTGCCCCAGCCAGTTCTAGCCTCTCCTCTCTAATGATGTC... |
Task1_train_45537 | A genomic variant on Chromosome 17 is under review. What is the biological outcome — benign or pathogenic? | Benign | TAAACTGTACCTATCAGCCATCTTCAGTTGGGTTGGAATGGCCTGCACAATCCCATGCATGCACCTGACGCTTGCAGGGGCTCCCAGCTTGGCAGAGACGCCATTTCCATCGGGATCAGCTATCCCCCCACACCAATGCTGCAGCTCTCTGGATGGATGCACCCTGACCTCCCCTGTGTTAGAGGAGAGGTGGGCGTGTTGAATCATGGAGGCAGACTTCCCCTTTGCCGTTCTCGTGATAGTGACTGAGTTCTCAGGATCTGGTTGTTTAAAAGTGTGTAGCGCCTCCCCCTTCTCTCTCTCTCCTGCCACCATGTGAA... | TAAACTGTACCTATCAGCCATCTTCAGTTGGGTTGGAATGGCCTGCACAATCCCATGCATGCACCTGACGCTTGCAGGGGCTCCCAGCTTGGCAGAGACGCCATTTCCATCGGGATCAGCTATCCCCCCACACCAATGCTGCAGCTCTCTGGATGGATGCACCCTGACCTCCCCTGTGTTAGAGGAGAGGTGGGCGTGTTGAATCATGGAGGCAGACTTCCCCTTTGCCGTTCTCGTGATAGTGACTGAGTTCTCAGGATCTGGTTGTTTAAAAGTGTGTAGCGCCTCCCCCTTCTCTCTCTCTCCTGCCACCATGTGAA... |
Task1_train_45538 | A variant was discovered on Chromosome 17. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TCAGTGACAACCAGTCAGGTGAGCAAAGCCAGCCCCCACCCCCACCAGCCTGTAGCCCCTGCCCAGCCTCCTACCCCTCCCATGTCCTCTCCATCCTGCCTCCCCAGCGCCACCCCACTCCATGAGTGGAGAGGGGCTCCCTCTCTAGACCCAGAGCTGGAGCCTTGGCCCTCCTTCCTCCCCAGTCTCCCAGTCCTGATGGTCTGTGTCCTCAGAGGCAGAGTGAGGGCTCTGTGGTTCAAATGCAACCCCCAGGGGTGTATGGAGACTAGCCAGCCCCCTGAGGTTCCACACCAAGGCATCAGGGGGGCCACTGGGCT... | TCAGTGACAACCAGTCAGGTGAGCAAAGCCAGCCCCCACCCCCACCAGCCTGTAGCCCCTGCCCAGCCTCCTACCCCTCCCATGTCCTCTCCATCCTGCCTCCCCAGCGCCACCCCACTCCATGAGTGGAGAGGGGCTCCCTCTCTAGACCCAGAGCTGGAGCCTTGGCCCTCCTTCCTCCCCAGTCTCCCAGTCCTGATGGTCTGTGTCCTCAGAGGCAGAGTGAGGGCTCTGTGGTTCAAATGCAACCCCCAGGGGTGTATGGAGACTAGCCAGCCCCCTGAGGTTCCACACCAAGGCATCAGGGGGGCCACTGGGCT... |
Task1_train_45539 | A genetic alteration is present on Chromosome 17. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TGGATTCTCCTCCTCCTCCTCCTCTTTATCATCTTGCACTTCAGTAAGTCGCATACTGTAGACCCAAAGGAAAGTAGGGGGCTCAGAGACCCAGATTGCCTGGAGCCCTTGCTGCCCTACTCAGGCTCTGGTAGTACCCACCCTAACACTTCCTCAGAGTGGCAGCATTCCCTTTGGTGCACACGTGCCCCTTACCGCTTTTGGTCCCTTAGACCCTGATGTCCCCTGACTCCTGCCAGCTCCTCTGGATCCAGGTCACTATCCAGAGATGTGTCATCACCGTCGTCCTCAACATCTGACACATAGATATCATCCCTTGG... | TGGATTCTCCTCCTCCTCCTCCTCTTTATCATCTTGCACTTCAGTAAGTCGCATACTGTAGACCCAAAGGAAAGTAGGGGGCTCAGAGACCCAGATTGCCTGGAGCCCTTGCTGCCCTACTCAGGCTCTGGTAGTACCCACCCTAACACTTCCTCAGAGTGGCAGCATTCCCTTTGGTGCACACGTGCCCCTTACCGCTTTTGGTCCCTTAGACCCTGATGTCCCCTGACTCCTGCCAGCTCCTCTGGATCCAGGTCACTATCCAGAGATGTGTCATCACCGTCGTCCTCAACATCTGACACATAGATATCATCCCTTGG... |
Task1_train_45540 | This variant is present on Chromosome 17. Is the change likely to result in a pathogenic outcome? | Benign | CAGTCCCTGCGTTGGGGAACTCCAAGCTCTACCCCAGCTCCTTTCACCTCTTCAATTCCGCCACCTCCTGGGCCTTCATTTCTGCCAAGGTCTGGTTCAGTTGTTCCTCCTCCTCCTCTTCCTCCTCCTCCTTAGAGGGCTGCTTTGTGGTTCCAGCTGTTGAGTCCTCCTCATCACCTTCATCTTCCTCTCCAGAGCTGAGGCTGGCAAAACAGTCCCAAGAGTTGGGTTATTTTCCCAGACTTTTCCCCTGGACACCCAGTCCACACCTGCCTCGCTGCGTTCTCTCCTCACCTGATGTCCAGTGCCTTTGCTTGTTC... | CAGTCCCTGCGTTGGGGAACTCCAAGCTCTACCCCAGCTCCTTTCACCTCTTCAATTCCGCCACCTCCTGGGCCTTCATTTCTGCCAAGGTCTGGTTCAGTTGTTCCTCCTCCTCCTCTTCCTCCTCCTCCTTAGAGGGCTGCTTTGTGGTTCCAGCTGTTGAGTCCTCCTCATCACCTTCATCTTCCTCTCCAGAGCTGAGGCTGGCAAAACAGTCCCAAGAGTTGGGTTATTTTCCCAGACTTTTCCCCTGGACACCCAGTCCACACCTGCCTCGCTGCGTTCTCTCCTCACCTGATGTCCAGTGCCTTTGCTTGTTC... |
Task1_train_45541 | Chromosome 17 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CTGAGTTATTAACTGCAAAATAGCCAAAAATGAACACAAGTGGGTCTCGTTATCAAAAAAATTCATTATGGCACATAAGAATCAGAACTTCTAAAGAAGATTAATTAGGGGGTTGATTATTTGCATTGTAAAATAATTCCTGACTTCATGAAATCATTTTTGGATACTAGAGTTCCTGTGAGCATCTTAGTATAGATTTAGGTCACCAGTCACTTAGCCAAGGTGCTTGGGAGAGTAAACTCTTAACTAACCACCGCTCTTTAGTGCTTATTTGGAAATAATAAACATCTCAGATGTTTATTATTATTATAAAACATCCA... | CTGAGTTATTAACTGCAAAATAGCCAAAAATGAACACAAGTGGGTCTCGTTATCAAAAAAATTCATTATGGCACATAAGAATCAGAACTTCTAAAGAAGATTAATTAGGGGGTTGATTATTTGCATTGTAAAATAATTCCTGACTTCATGAAATCATTTTTGGATACTAGAGTTCCTGTGAGCATCTTAGTATAGATTTAGGTCACCAGTCACTTAGCCAAGGTGCTTGGGAGAGTAAACTCTTAACTAACCACCGCTCTTTAGTGCTTATTTGGAAATAATAAACATCTCAGATGTTTATTATTATTATAAAACATCCA... |
Task1_train_45542 | Consider this mutation on Chromosome 17. Is this a benign change or a disease-causing variant? | Benign | CCATACATCTTGCTCATGGTGTTGGCAAGCAGCCCCTCCTTCTCAGGGGCGTCATCCCCGCTGCCGTCGTGGCTGTGGCGGTACATGTAGGATGCCTGCTTCATGGAGCGCTGTAGCAGGTGCCGGCGGTAGGCCCTCTGGATCTTGATGGCGCACACCTCCTCGTGCTTCCTCTTGAGGGTGGTGGTGATGGGCTCGTAGGACACCTTGGAGGGGTTGGCTGCCATGAACTTCTCCTCCATGGTCTGCTTGAGGGCGTCCATTTCCCCAGAGTCACCCAGGACCTCTTTGGTCAGGGCAAAGAGGATGTCCAGGCAGTG... | CCATACATCTTGCTCATGGTGTTGGCAAGCAGCCCCTCCTTCTCAGGGGCGTCATCCCCGCTGCCGTCGTGGCTGTGGCGGTACATGTAGGATGCCTGCTTCATGGAGCGCTGTAGCAGGTGCCGGCGGTAGGCCCTCTGGATCTTGATGGCGCACACCTCCTCGTGCTTCCTCTTGAGGGTGGTGGTGATGGGCTCGTAGGACACCTTGGAGGGGTTGGCTGCCATGAACTTCTCCTCCATGGTCTGCTTGAGGGCGTCCATTTCCCCAGAGTCACCCAGGACCTCTTTGGTCAGGGCAAAGAGGATGTCCAGGCAGTG... |
Task1_train_45543 | A sequence alteration has been identified on Chromosome 17. Is it disease-inducing or harmless? | Benign | GTATCCTTGGGGGGGGTCCTGAAACCAATGCCCCCTTGGATACTGTACATAAATGTGTGTGTGCATATAACTTACAAACTATATAAGTTCTAATTGTACTTTTATAGTGTGTATACACATAACCAGAAATTTTAATATGCAAAAAAATAATAATAAATAGAAGTTCTAGGCTGGACACAGCGGCTCACACCTGTAATCCCAGCACTTTGGAAGGCTGAAGCAGGAGGATCACTTGAGCCCAGAAGTTTGAGACCACACTAGGCAACATAGTGAGACTCCGTCTCAATCGACAGATTAGACAGCTAGATGAATGTTTCTTC... | GTATCCTTGGGGGGGGTCCTGAAACCAATGCCCCCTTGGATACTGTACATAAATGTGTGTGTGCATATAACTTACAAACTATATAAGTTCTAATTGTACTTTTATAGTGTGTATACACATAACCAGAAATTTTAATATGCAAAAAAATAATAATAAATAGAAGTTCTAGGCTGGACACAGCGGCTCACACCTGTAATCCCAGCACTTTGGAAGGCTGAAGCAGGAGGATCACTTGAGCCCAGAAGTTTGAGACCACACTAGGCAACATAGTGAGACTCCGTCTCAATCGACAGATTAGACAGCTAGATGAATGTTTCTTC... |
Task1_train_45544 | A mutation on Chromosome 17 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TGTGGGCACCTCAGATCATAGAAGTAGAGACTTTCTTTTCTTTTTTTTTTTTTTTTTTGAGACAGAGTCTCACTCTTTCACCCAGGCTGGAGTGCAGTGGTGTGATCTCAGCTCACTGCAACCTCCACCTCCCGGGTTCAAGTGATTCTCCTGCCTAAGCCTCCTGAGTAGCTGGGATTACAGGTGTGCACCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATATTGGCCAGGCTGGTTTTGAACTCCTGACCTCAAGCGATCCGCCCACC... | TGTGGGCACCTCAGATCATAGAAGTAGAGACTTTCTTTTCTTTTTTTTTTTTTTTTTTGAGACAGAGTCTCACTCTTTCACCCAGGCTGGAGTGCAGTGGTGTGATCTCAGCTCACTGCAACCTCCACCTCCCGGGTTCAAGTGATTCTCCTGCCTAAGCCTCCTGAGTAGCTGGGATTACAGGTGTGCACCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATATTGGCCAGGCTGGTTTTGAACTCCTGACCTCAAGCGATCCGCCCACC... |
Task1_train_45545 | A mutation found on Chromosome 17 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TAGTCTTGAACTCCTGACCTCAAGTGATCTGCCTGCCTTGGCCTCCCAAAGTGCTGGAATTACAGGTGTGAGCCACCGTGCCTGACCACTCTCTTTGATTCCAGATAATTACAAAAAGTAAAGGCGAAATCAATCCCTGCGTTTGTAACTCGAAGCTGGCCTAAGATCAACGCCAGGGTGTGCTCTATCTTCCTTGATGGGTGGCAGCTTTCCTGACAAAAACCAGGGCCCCTCCTCACCCCATCTTCCCCTCCCATCCTGGGCAGCAGCACCAGAGGCTCCAAAAGAACCTACCTTATCCCACAAAAAAATTTTTGCAG... | TAGTCTTGAACTCCTGACCTCAAGTGATCTGCCTGCCTTGGCCTCCCAAAGTGCTGGAATTACAGGTGTGAGCCACCGTGCCTGACCACTCTCTTTGATTCCAGATAATTACAAAAAGTAAAGGCGAAATCAATCCCTGCGTTTGTAACTCGAAGCTGGCCTAAGATCAACGCCAGGGTGTGCTCTATCTTCCTTGATGGGTGGCAGCTTTCCTGACAAAAACCAGGGCCCCTCCTCACCCCATCTTCCCCTCCCATCCTGGGCAGCAGCACCAGAGGCTCCAAAAGAACCTACCTTATCCCACAAAAAAATTTTTGCAG... |
Task1_train_45546 | Here’s a variant located on Chromosome 17. What is the predicted biological effect — harmless or disease-causing? | Benign | TACACATAGTACATGATATGAATTAAGTATTGATAAACAGACTTACTTCTTCTCTAAACTGAAGAGGAATCATTTCAAACTTCTTAAAAATTTCAATCCTAGAAATTTCTTAAGTTTTGGATAAAAACAGTTCCACTTTCATCTTTCTTTTTTTGTAAATCATTGTTCACCTGGATATTCATGTAATTTTTAAAAATACTTAAATAACCACCTTTAGCTAGAGTCACAGAACAAAAAAAAAAGAGAGAAAACCCCACAAATTTAAATCCTCAGCTTCTGTTAATTATTCATGATCAACCACAGTCTTCATTAATACATAT... | TACACATAGTACATGATATGAATTAAGTATTGATAAACAGACTTACTTCTTCTCTAAACTGAAGAGGAATCATTTCAAACTTCTTAAAAATTTCAATCCTAGAAATTTCTTAAGTTTTGGATAAAAACAGTTCCACTTTCATCTTTCTTTTTTTGTAAATCATTGTTCACCTGGATATTCATGTAATTTTTAAAAATACTTAAATAACCACCTTTAGCTAGAGTCACAGAACAAAAAAAAAAGAGAGAAAACCCCACAAATTTAAATCCTCAGCTTCTGTTAATTATTCATGATCAACCACAGTCTTCATTAATACATAT... |
Task1_train_45547 | A change on Chromosome 17 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CCAACAGTATTTCACCCAGTATTTTAGAATCCATTGATGACTGTTGCTTGAATCAATGATATCGGGGTTTGCAATATCATGAAATGGTGAATTTTCTAATGTATCTTTCCTTCTACATTTATTCCATAGCTTCTGTAAAAACATAAGCTTTCTCTACCTCTTCCCCCCGCCCCCGACCTCTAGGGTCAATTATTTGTTTTTGATTAATACTATTGACTCTTAGATTTTAGTCAATGTGTTATGATCCATTACCATTAATATGTATCTTAATGTTCAATTTGTCCTAGATGTGGCCAGTGACAACCCTCCTCAAGCCAGCA... | CCAACAGTATTTCACCCAGTATTTTAGAATCCATTGATGACTGTTGCTTGAATCAATGATATCGGGGTTTGCAATATCATGAAATGGTGAATTTTCTAATGTATCTTTCCTTCTACATTTATTCCATAGCTTCTGTAAAAACATAAGCTTTCTCTACCTCTTCCCCCCGCCCCCGACCTCTAGGGTCAATTATTTGTTTTTGATTAATACTATTGACTCTTAGATTTTAGTCAATGTGTTATGATCCATTACCATTAATATGTATCTTAATGTTCAATTTGTCCTAGATGTGGCCAGTGACAACCCTCCTCAAGCCAGCA... |
Task1_train_45548 | This alteration on Chromosome 17 may affect genome function. Does it lead to a disease or is it benign? | Benign | GCAGAGTAAGGGTGACTTGGTGAGTACATCCAATTGTTGACATAGTTTTGGGTGGGAGAAATTTTGCTATTATATCCACTTCTTAAAATAGTCTAGTGGGATTAACTTGGTTTCAATTCACAGAGATCTGGAAGCGAGGATCCTTTAAAAATCCTGAAATATACACTGCAGTAAAAGAACAAAGCATACACCTCAGCCTTAAATGACTGAAGTATGTCAAGTAGCAGCAGGTGGGAAAGTGGCTTTGGTTTTCAGTTTGTGAGCTCTGAATCCACACAAAGACAGGACTGCATTCTGAAAACCTGAATTAATTATTGTCC... | GCAGAGTAAGGGTGACTTGGTGAGTACATCCAATTGTTGACATAGTTTTGGGTGGGAGAAATTTTGCTATTATATCCACTTCTTAAAATAGTCTAGTGGGATTAACTTGGTTTCAATTCACAGAGATCTGGAAGCGAGGATCCTTTAAAAATCCTGAAATATACACTGCAGTAAAAGAACAAAGCATACACCTCAGCCTTAAATGACTGAAGTATGTCAAGTAGCAGCAGGTGGGAAAGTGGCTTTGGTTTTCAGTTTGTGAGCTCTGAATCCACACAAAGACAGGACTGCATTCTGAAAACCTGAATTAATTATTGTCC... |
Task1_train_45549 | The following genetic variant occurs on Chromosome 17. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GATCTTCCTCCCAGACAACTTGACTCCACAAGCATAAAGACACTGAAACACCTCCCTGGAACCTGTGTTTCCTTGCAAAAGTCAACCTGGTTCCACTTAGGTGTAGACCAGATGTCTGAGTAAAACTGGTTCCCAAGCCACAAGCGCGCCCCCTGGTGGTTGGAGAACAAGCCCTTCCTCTCCTCGCCAACAGTCAACTCTCTCTGCCGCCCCTAAAATCATGGCCCGCTAGGCTCAGACCTGGCCACCCTGAGAGGCTCAAGATCAACCATCTGGTGCCCACCTCTCTTCCTGCTGCTGGGCACTAGAGACCACATCCT... | GATCTTCCTCCCAGACAACTTGACTCCACAAGCATAAAGACACTGAAACACCTCCCTGGAACCTGTGTTTCCTTGCAAAAGTCAACCTGGTTCCACTTAGGTGTAGACCAGATGTCTGAGTAAAACTGGTTCCCAAGCCACAAGCGCGCCCCCTGGTGGTTGGAGAACAAGCCCTTCCTCTCCTCGCCAACAGTCAACTCTCTCTGCCGCCCCTAAAATCATGGCCCGCTAGGCTCAGACCTGGCCACCCTGAGAGGCTCAAGATCAACCATCTGGTGCCCACCTCTCTTCCTGCTGCTGGGCACTAGAGACCACATCCT... |
Task1_train_45550 | A change on Chromosome 17 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TTTTGTACTCCCATACAATGGAATACTACTAAGCAATAAAAAGGAACAGATTACAGTGACACACAACAACATGAGTGAATCTCTAATGCATTATGCAAAGGGAAAGAAGCCAGACTCAAAAAGCTAACTACTGAATATTTACATGACATTCCAGAAAAGGAGAACCTATGGTCACAGAAAATACATGAGTGATTACTAGGAGCTGGGACATGAGAAAAGAAGTGGAGCTGATGACAAAGGTCTGGAGAAATGTTTGAGGTGATGGAACTGTTCTTCATCTTGATGTGGTGATGGTTTGTCAAAACTTGCAGAACTGCACA... | TTTTGTACTCCCATACAATGGAATACTACTAAGCAATAAAAAGGAACAGATTACAGTGACACACAACAACATGAGTGAATCTCTAATGCATTATGCAAAGGGAAAGAAGCCAGACTCAAAAAGCTAACTACTGAATATTTACATGACATTCCAGAAAAGGAGAACCTATGGTCACAGAAAATACATGAGTGATTACTAGGAGCTGGGACATGAGAAAAGAAGTGGAGCTGATGACAAAGGTCTGGAGAAATGTTTGAGGTGATGGAACTGTTCTTCATCTTGATGTGGTGATGGTTTGTCAAAACTTGCAGAACTGCACA... |
Task1_train_45551 | The following genetic variant occurs on Chromosome 17. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GCCAGGCTGGCCTCCTGACCTCAAGTGATCCGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAAGTGTGAGCCACTGCGCCTGGCCAAGATCCTCATTTTCAAGAGATAAAATTAAAGGTTCTATATACAGTGAAGACTGTTCTATAACAGTCAAGATTAAAGGGGAAAAAACAGTATCGGCCCTTTACAGTACTGCATCTGTCCAAAGACCATAAGGGAGAAGATCCTGAAGAAATATATCAACAAAGCTAAGACTTTTTTCAATTATTCTTTTCTCACATTTTTTCTACTGATTTTTATTTAAGCTTATTGTATTT... | GCCAGGCTGGCCTCCTGACCTCAAGTGATCCGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAAGTGTGAGCCACTGCGCCTGGCCAAGATCCTCATTTTCAAGAGATAAAATTAAAGGTTCTATATACAGTGAAGACTGTTCTATAACAGTCAAGATTAAAGGGGAAAAAACAGTATCGGCCCTTTACAGTACTGCATCTGTCCAAAGACCATAAGGGAGAAGATCCTGAAGAAATATATCAACAAAGCTAAGACTTTTTTCAATTATTCTTTTCTCACATTTTTTCTACTGATTTTTATTTAAGCTTATTGTATTT... |
Task1_train_45552 | A variant was discovered on Chromosome 17. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | ACATTCTACAAGACAACTAGCCTGTACTCTTCAAAAATGTCAATGAAAGACAACAAAAGAGGCAAGGACTTATTCTTAATTATAGGAGACTAGGCTCACGCCTGTAATCCCAGCAGTTTGGGAGGCTGAGGCAGGCGGATCATTTTAGTTCGGGAGTTTGAGACCAGCCTGGCCAACACAGTGAAATCCCATCTCTACTAAAATTATAAAAATTAGCTGGGCGTGGTGGCAGGTGCCTATATTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTCAAACCTGGGAGGTAGATGTTGCAGTGAGCCAAAATTGCAC... | ACATTCTACAAGACAACTAGCCTGTACTCTTCAAAAATGTCAATGAAAGACAACAAAAGAGGCAAGGACTTATTCTTAATTATAGGAGACTAGGCTCACGCCTGTAATCCCAGCAGTTTGGGAGGCTGAGGCAGGCGGATCATTTTAGTTCGGGAGTTTGAGACCAGCCTGGCCAACACAGTGAAATCCCATCTCTACTAAAATTATAAAAATTAGCTGGGCGTGGTGGCAGGTGCCTATATTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTCAAACCTGGGAGGTAGATGTTGCAGTGAGCCAAAATTGCAC... |
Task1_train_45553 | A change on Chromosome 17 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TCAATGAAAGACAACAAAAGAGGCAAGGACTTATTCTTAATTATAGGAGACTAGGCTCACGCCTGTAATCCCAGCAGTTTGGGAGGCTGAGGCAGGCGGATCATTTTAGTTCGGGAGTTTGAGACCAGCCTGGCCAACACAGTGAAATCCCATCTCTACTAAAATTATAAAAATTAGCTGGGCGTGGTGGCAGGTGCCTATATTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTCAAACCTGGGAGGTAGATGTTGCAGTGAGCCAAAATTGCACCACTGCACTCCAGCCTGGGTGACAGAGTGAGACACCATT... | TCAATGAAAGACAACAAAAGAGGCAAGGACTTATTCTTAATTATAGGAGACTAGGCTCACGCCTGTAATCCCAGCAGTTTGGGAGGCTGAGGCAGGCGGATCATTTTAGTTCGGGAGTTTGAGACCAGCCTGGCCAACACAGTGAAATCCCATCTCTACTAAAATTATAAAAATTAGCTGGGCGTGGTGGCAGGTGCCTATATTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTCAAACCTGGGAGGTAGATGTTGCAGTGAGCCAAAATTGCACCACTGCACTCCAGCCTGGGTGACAGAGTGAGACACCATT... |
Task1_train_45554 | Consider a variant on Chromosome 17. Determine its clinical classification and disease relevance. | Benign | CAGGCAGTTGGAGTCAGACAGTGGCTGTCATTTCAAAGGCTTCCCTGCTCATTGGTGTGGCAATTGCATCCACTGAGACTTCAGCTAAGGTTGTCACTAGAACATCTTTGCACACGGTCTCTTCTTAAGGCCTGGTCTTCCTCATAGGGTGACAGCTTGGTTTTAAGAGTGAGGGTCCCAAGAGACAGGCAGAAGCTTCATTGCCTTTCTGGAAGCAGCCTTTGAAGTTACCTGATGTCATTTCCATCATAATCCCCAGACAACCTAGGTTTATAGAGAAGAGAACGTAGATCCCACCATCTCAGATGTGAGGAGTGTCA... | CAGGCAGTTGGAGTCAGACAGTGGCTGTCATTTCAAAGGCTTCCCTGCTCATTGGTGTGGCAATTGCATCCACTGAGACTTCAGCTAAGGTTGTCACTAGAACATCTTTGCACACGGTCTCTTCTTAAGGCCTGGTCTTCCTCATAGGGTGACAGCTTGGTTTTAAGAGTGAGGGTCCCAAGAGACAGGCAGAAGCTTCATTGCCTTTCTGGAAGCAGCCTTTGAAGTTACCTGATGTCATTTCCATCATAATCCCCAGACAACCTAGGTTTATAGAGAAGAGAACGTAGATCCCACCATCTCAGATGTGAGGAGTGTCA... |
Task1_train_45555 | This variant is present on Chromosome 17. Is the change likely to result in a pathogenic outcome? | Benign | AAGTCATTGGCAAAAGCACTGACTTCCTCACGCCTGATGAGAAGAAGCCTGTGGTGCATTTGAACAACAGCCTTGTCAGCTCCCCGCTCCGGAGGCCCCAGGCAGCCGCCTTCCATCTCCAGGGCCCGGAGCTTCCACACCTCGGGGCCAGGGAGCGTTTGCAGAAGCAGCACCTCCTGGTAGGCCCCTACACAAGGGCAGCTGTTGTGACGGGAGGTGTGGATGTGGAACAAATGCTCAGAAGCCCCGTGGTGGCTCTTGGTGGCATGTGATAGTTAGAGTCTGCAGGGACAGTCTGAGTCCCTCCCTGGCCTAGAAAT... | AAGTCATTGGCAAAAGCACTGACTTCCTCACGCCTGATGAGAAGAAGCCTGTGGTGCATTTGAACAACAGCCTTGTCAGCTCCCCGCTCCGGAGGCCCCAGGCAGCCGCCTTCCATCTCCAGGGCCCGGAGCTTCCACACCTCGGGGCCAGGGAGCGTTTGCAGAAGCAGCACCTCCTGGTAGGCCCCTACACAAGGGCAGCTGTTGTGACGGGAGGTGTGGATGTGGAACAAATGCTCAGAAGCCCCGTGGTGGCTCTTGGTGGCATGTGATAGTTAGAGTCTGCAGGGACAGTCTGAGTCCCTCCCTGGCCTAGAAAT... |
Task1_train_45556 | Here’s a variant located on Chromosome 17. What is the predicted biological effect — harmless or disease-causing? | Benign | ATTCATGGTATACTGATATGTAAGAAAGCAAGGTGCTAGGTGATGATCACATTATGACTTTTTAATTTTTAAAGGAAAAACTCTACGTATTATAAGCACTTATGTTTGTCACTGTAAAGGCACAGAAGACCTTTCTCATACAGCAAACTAATAACAATAACTTCTTCAGATGGGGGAAGGATAAATTTTTCCTCTATATTATTTGACTTATTACTGTTTGCTCATTGTAATTTTAAAATTCCCATAGATAGCAGGGATTTTTTTAAAAGAAAATTCTACTAGATATCTCTTAATTTCTAGTTAACTCTCAAAGCACACAA... | ATTCATGGTATACTGATATGTAAGAAAGCAAGGTGCTAGGTGATGATCACATTATGACTTTTTAATTTTTAAAGGAAAAACTCTACGTATTATAAGCACTTATGTTTGTCACTGTAAAGGCACAGAAGACCTTTCTCATACAGCAAACTAATAACAATAACTTCTTCAGATGGGGGAAGGATAAATTTTTCCTCTATATTATTTGACTTATTACTGTTTGCTCATTGTAATTTTAAAATTCCCATAGATAGCAGGGATTTTTTTAAAAGAAAATTCTACTAGATATCTCTTAATTTCTAGTTAACTCTCAAAGCACACAA... |
Task1_train_45557 | Consider this mutation on Chromosome 17. Is this a benign change or a disease-causing variant? | Benign | CCTCCCAAAGTGCTGGGATTACCAGCATGAGCCACCACACCCGGCCAATTAAACCTTTTTAAAACCAACTGAAAAATGTTTAAAATTCGCTTGCTTGTGAGCCGTCATTGGTGAATATTGGTTCCAAGGTTTGGGGAATGAATTTGAGAAAGCCTTTTTCTCAAACCTTTAGGGCTCAGTAAGGCTAAAACAAAAACAAACAGGTGCATCCAAGATCTGATTTCAAGTCAAGATTTATTGCTTTACAAACAAACATTATACTTGGTCTTAATAGAAAAATGACACCAGATACATCCAAAATACATTTCACATTGGGATAG... | CCTCCCAAAGTGCTGGGATTACCAGCATGAGCCACCACACCCGGCCAATTAAACCTTTTTAAAACCAACTGAAAAATGTTTAAAATTCGCTTGCTTGTGAGCCGTCATTGGTGAATATTGGTTCCAAGGTTTGGGGAATGAATTTGAGAAAGCCTTTTTCTCAAACCTTTAGGGCTCAGTAAGGCTAAAACAAAAACAAACAGGTGCATCCAAGATCTGATTTCAAGTCAAGATTTATTGCTTTACAAACAAACATTATACTTGGTCTTAATAGAAAAATGACACCAGATACATCCAAAATACATTTCACATTGGGATAG... |
Task1_train_45558 | This mutation on Chromosome 17 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TGAGGGCTCTCTTCTGAAGGAGGACCCATTACATGAAGGTAGACCTTTCATGTCTTGTTGCCGACGTCCAAGTCTCTTGCGGTCCAGAAATGCCAGGATGGTTGTTTCAAATGCATTGGGTATGAATTGCACCTTGAATCTGCCCTTCCCTTTTTCGATTAAACCTTTTCACATAGCTGCTGCTGCTCCTTAGCAGTCCATCCCCTGGACGGAGGCGGCCTCTCAGGACCTGGAGCAGAGCTGTAGGGAGCTGCCGTCTCTTATGGTAGATGTGGCCCATCACAATATACCTGCTGCCTGGACAAAATAACCAGAACATT... | TGAGGGCTCTCTTCTGAAGGAGGACCCATTACATGAAGGTAGACCTTTCATGTCTTGTTGCCGACGTCCAAGTCTCTTGCGGTCCAGAAATGCCAGGATGGTTGTTTCAAATGCATTGGGTATGAATTGCACCTTGAATCTGCCCTTCCCTTTTTCGATTAAACCTTTTCACATAGCTGCTGCTGCTCCTTAGCAGTCCATCCCCTGGACGGAGGCGGCCTCTCAGGACCTGGAGCAGAGCTGTAGGGAGCTGCCGTCTCTTATGGTAGATGTGGCCCATCACAATATACCTGCTGCCTGGACAAAATAACCAGAACATT... |
Task1_train_45559 | A variant on Chromosome 17 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GCGGACGTGGCGGAAGCCGCGGGGTCCGCGGGGTCGGTGCCTCTAGGGAGCCAGGGAGGCCTTTCCCGAGGCTCCTGGGGAAGAAGAGGCGAAGCGAGAGTCCCTGGGGAACCCCCACTCCACTCCCAGCTGGAGACTGGGTTGTGTCTGCATGGACCAGAGCCCACAGTGCGAGTTGCTATAGGCAACCAGCCAGGGTGGCCAGCTCCTTCCCGTTTGCCCGTGATGTTCTGGTTTTGGGACCAAAGCATCCTAGGCCTCCAGCCCACTGCAGTGACCGAATTCTGCGCCCCCTGCCCATCTTCTCCCGCAGCTTCCCT... | GCGGACGTGGCGGAAGCCGCGGGGTCCGCGGGGTCGGTGCCTCTAGGGAGCCAGGGAGGCCTTTCCCGAGGCTCCTGGGGAAGAAGAGGCGAAGCGAGAGTCCCTGGGGAACCCCCACTCCACTCCCAGCTGGAGACTGGGTTGTGTCTGCATGGACCAGAGCCCACAGTGCGAGTTGCTATAGGCAACCAGCCAGGGTGGCCAGCTCCTTCCCGTTTGCCCGTGATGTTCTGGTTTTGGGACCAAAGCATCCTAGGCCTCCAGCCCACTGCAGTGACCGAATTCTGCGCCCCCTGCCCATCTTCTCCCGCAGCTTCCCT... |
Task1_train_45560 | A mutation has occurred on Chromosome 17. What is the medical relevance of this mutation? | Benign | ACTAGACTGGAGAGGAGAAAGAGACAAACACCCAATATACTTGTTCTTCTTGGGCTAAGCCTGTCCTAGCAGAGGACCTAAAACCTGGGACATTTCGATGCATACTTCTTTGAAAAGGTAATATTCTTCGGTAGGAAGGAACTGTATTATTTTCACTTGAGTTCACTTTAGGTTTTTTTTTTTTTTTTTTAGACAGAGTTTTATTCTTGTTGCCCCAGGTGGAGTGCGATGGTGCAATCTCAGGTCACTGCAACCTCTGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAATAGCTGGGATTAGAGGTGTC... | ACTAGACTGGAGAGGAGAAAGAGACAAACACCCAATATACTTGTTCTTCTTGGGCTAAGCCTGTCCTAGCAGAGGACCTAAAACCTGGGACATTTCGATGCATACTTCTTTGAAAAGGTAATATTCTTCGGTAGGAAGGAACTGTATTATTTTCACTTGAGTTCACTTTAGGTTTTTTTTTTTTTTTTTTAGACAGAGTTTTATTCTTGTTGCCCCAGGTGGAGTGCGATGGTGCAATCTCAGGTCACTGCAACCTCTGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAATAGCTGGGATTAGAGGTGTC... |
Task1_train_45561 | Mutation context: Chromosome 17. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTATAGGCGTGCGCCACCACGACCAGCCAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACTGTGTTGGCCAGGATGGTCTCGATCTCCTGACCTCCTGATCTGCCTGCCTCGGCCTCTCAAAGTACTGGGATTACAGGCATGAGCCACTGCACCTGGCCTTTTTTTGTGTGTTTTAAGTAGAGACAGGTTTTTGCCATGTTGGCCAGGCTGGTCTCGATCACCTGACCTCAGGTGATCCGCCCACCTCAGCCTCCCAAAGTGCTGGGATTA... | CCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTATAGGCGTGCGCCACCACGACCAGCCAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACTGTGTTGGCCAGGATGGTCTCGATCTCCTGACCTCCTGATCTGCCTGCCTCGGCCTCTCAAAGTACTGGGATTACAGGCATGAGCCACTGCACCTGGCCTTTTTTTGTGTGTTTTAAGTAGAGACAGGTTTTTGCCATGTTGGCCAGGCTGGTCTCGATCACCTGACCTCAGGTGATCCGCCCACCTCAGCCTCCCAAAGTGCTGGGATTA... |
Task1_train_45562 | Consider a variant on Chromosome 17. Determine its clinical classification and disease relevance. | Benign | ACCTGCACAACTGTACATGACCATCCCTGGGAGAGTTGGCATCAGGCACTGCAAATCATTGCTGTACGAAAAAACTAGGCAAGAATGGAGATGTTTTCTATCTGCACTGTCCAAGCTGCTAGCCTCTAGCCACCTGCTGCTGCTGAGCATTTGAAATGTGGCTAGGAATTTATGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTATTTTATTGTGGGTATGTATATATACAGATATATATAATCATAAAATGTTACCATCTTAACCATTTTAAATGTAAAGTTCTGTCGCATTAAACATTCACTTTGTTTTGCAACAAT... | ACCTGCACAACTGTACATGACCATCCCTGGGAGAGTTGGCATCAGGCACTGCAAATCATTGCTGTACGAAAAAACTAGGCAAGAATGGAGATGTTTTCTATCTGCACTGTCCAAGCTGCTAGCCTCTAGCCACCTGCTGCTGCTGAGCATTTGAAATGTGGCTAGGAATTTATGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTATTTTATTGTGGGTATGTATATATACAGATATATATAATCATAAAATGTTACCATCTTAACCATTTTAAATGTAAAGTTCTGTCGCATTAAACATTCACTTTGTTTTGCAACAAT... |
Task1_train_45563 | The following genetic variant occurs on Chromosome 17. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | AGCTGCTAGCCTCTAGCCACCTGCTGCTGCTGAGCATTTGAAATGTGGCTAGGAATTTATGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTATTTTATTGTGGGTATGTATATATACAGATATATATAATCATAAAATGTTACCATCTTAACCATTTTAAATGTAAAGTTCTGTCGCATTAAACATTCACTTTGTTTTGCAACAATTACCACTATCCATCTTCAGAACTGTTTCATTTTTTCTAACTGAAACTGTACCCATGAAACATAAACTGCCCAGTTTTTCTTCCCCGCAGTGCCCCGCCACTCACCATCCTACC... | AGCTGCTAGCCTCTAGCCACCTGCTGCTGCTGAGCATTTGAAATGTGGCTAGGAATTTATGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTATTTTATTGTGGGTATGTATATATACAGATATATATAATCATAAAATGTTACCATCTTAACCATTTTAAATGTAAAGTTCTGTCGCATTAAACATTCACTTTGTTTTGCAACAATTACCACTATCCATCTTCAGAACTGTTTCATTTTTTCTAACTGAAACTGTACCCATGAAACATAAACTGCCCAGTTTTTCTTCCCCGCAGTGCCCCGCCACTCACCATCCTACC... |
Task1_train_45564 | Given a variant located on Chromosome 17, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GTGATGCATTGTAGCAATTCTGATTTCTGTTACCTGAGAGTGTTGATTTTTGTTTTCACTGGCAGCTAATCAGTAGTCAGTTCCCTTGAACTTATAAAGCCTTAGTTTTACACTTTGTTAGGACGAGTCTTTCAGATTTTTCCCTTGATCTTAGGCAGATCCCTCAGTCCTGGGACACAGTCTCTACTCCTAGCATGAACTGTTTGTCAAAGCTCATGTCACTGCCCTGTACTGGCAATGAAGAATAATCAAATTCTATTCCAAACTGTAGGCAAAGACAACAACTATTAATCTCTACTGATCAACTTGACTCTCAGCCA... | GTGATGCATTGTAGCAATTCTGATTTCTGTTACCTGAGAGTGTTGATTTTTGTTTTCACTGGCAGCTAATCAGTAGTCAGTTCCCTTGAACTTATAAAGCCTTAGTTTTACACTTTGTTAGGACGAGTCTTTCAGATTTTTCCCTTGATCTTAGGCAGATCCCTCAGTCCTGGGACACAGTCTCTACTCCTAGCATGAACTGTTTGTCAAAGCTCATGTCACTGCCCTGTACTGGCAATGAAGAATAATCAAATTCTATTCCAAACTGTAGGCAAAGACAACAACTATTAATCTCTACTGATCAACTTGACTCTCAGCCA... |
Task1_train_45565 | A variant was discovered on Chromosome 17. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GATCACTTCCAAGAAGGATTCCAGCCTCCATGACACTGGGCCCGGCGCAGGCCAGGTTCCAAAGGTTCTCCGGGTCTTGCCGGCCAGGCGCCCTCTCTGAGCTTGCATTGACAGTGATCCACCATGCCCCCCACCCTGCCAGGTGGCTTTTTACCCTCTCCCAGGGAGCACTTTCAGAGTCCTTTCCAAATATCTAAAGTAAAGAAAACACTAGTGGCCTGGCATGGCGGCTCACGCCTAGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGAGAATCACTTGAGGCCAGGAGTTCAAGACCAGCCTGGCCAACATGGCG... | GATCACTTCCAAGAAGGATTCCAGCCTCCATGACACTGGGCCCGGCGCAGGCCAGGTTCCAAAGGTTCTCCGGGTCTTGCCGGCCAGGCGCCCTCTCTGAGCTTGCATTGACAGTGATCCACCATGCCCCCCACCCTGCCAGGTGGCTTTTTACCCTCTCCCAGGGAGCACTTTCAGAGTCCTTTCCAAATATCTAAAGTAAAGAAAACACTAGTGGCCTGGCATGGCGGCTCACGCCTAGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGAGAATCACTTGAGGCCAGGAGTTCAAGACCAGCCTGGCCAACATGGCG... |
Task1_train_45566 | A mutation on Chromosome 17 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TGTGCTATTCTTTGAATGTTTTTACCCAGATATTTTCCCATTTCTGTGTGTGATCTCCTGGTTCTTCATCCACAGGGAAGAAACATCTTGAAGCAGGAGAGACAGTGAATGAAGTGGGGAGCCCTATGCTGCAGTAGGGCCACAACAGTTAAGGAAATCTTTGGGATTAAGGTTTCTCTGTTAAAGAGTTGATTTAAAAAAAAATTTTTTTTTTTTTGTATTTTTTTGTAGAGACAGGGTTTTGTCATGTTACCCAGGCTGGTCTCGAGCTCCTGAGACCAAGCGATCTGCCTGTTTAGGCCCAAAGTGCTGGGATTACA... | TGTGCTATTCTTTGAATGTTTTTACCCAGATATTTTCCCATTTCTGTGTGTGATCTCCTGGTTCTTCATCCACAGGGAAGAAACATCTTGAAGCAGGAGAGACAGTGAATGAAGTGGGGAGCCCTATGCTGCAGTAGGGCCACAACAGTTAAGGAAATCTTTGGGATTAAGGTTTCTCTGTTAAAGAGTTGATTTAAAAAAAAATTTTTTTTTTTTTGTATTTTTTTGTAGAGACAGGGTTTTGTCATGTTACCCAGGCTGGTCTCGAGCTCCTGAGACCAAGCGATCTGCCTGTTTAGGCCCAAAGTGCTGGGATTACA... |
Task1_train_45567 | Here’s a variant located on Chromosome 17. What is the predicted biological effect — harmless or disease-causing? | Benign | AGAGATGTATTAGGCTGTGAGTTATGTTAATTTATTTTCCTGCAAAGGAAATGCTACAGGTTCTAGCAGTTTTTCCTCCCTGATACAAAAGAACTGAGAGTGGAGCTCATCCATTGCATATTAGCTTCCAGTTTTAAAAAATGAAAGGCATCCGGCCAGGTGCATTGGCTCACGCCTGGAATCCCAGCACATTGGGAGGCCAAGACAGGGGAATCGCCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACGTGGTGAAACCCTGTCTCTACTAAATATACAAAGTTAGCCAGGTGTGGTGGTACACATCTATAATCCCA... | AGAGATGTATTAGGCTGTGAGTTATGTTAATTTATTTTCCTGCAAAGGAAATGCTACAGGTTCTAGCAGTTTTTCCTCCCTGATACAAAAGAACTGAGAGTGGAGCTCATCCATTGCATATTAGCTTCCAGTTTTAAAAAATGAAAGGCATCCGGCCAGGTGCATTGGCTCACGCCTGGAATCCCAGCACATTGGGAGGCCAAGACAGGGGAATCGCCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACGTGGTGAAACCCTGTCTCTACTAAATATACAAAGTTAGCCAGGTGTGGTGGTACACATCTATAATCCCA... |
Task1_train_45568 | This is a variant located on Chromosome 17. Is this mutation a likely cause of disease or not? | Benign | TTCCTTATGTGTAATTTGGTCATGTCACTCCTTCCCCAAAAGCTGTTGTCATCTTTCTCTGGATGTGTTCACTGAAAAGTCTACATACTTGCCTTTAGTTCCGTTCATTGTTTTTGTTAAGAAAGATTTTTTTTGAATCCCATTCTTTTATGTCAGAATAATTCACTTTCCTTTCCTCATCAATTTCTTTTCTTTTGTTTTACAATATTCTTTGAAAACTATAATGAAATAATAATTTTAAAAAACAAAAACAAAACAGCTGCAAAGCCAACACAATAATAACTCACACACATAGCAATTAATATGCATTGAAGAAAACT... | TTCCTTATGTGTAATTTGGTCATGTCACTCCTTCCCCAAAAGCTGTTGTCATCTTTCTCTGGATGTGTTCACTGAAAAGTCTACATACTTGCCTTTAGTTCCGTTCATTGTTTTTGTTAAGAAAGATTTTTTTTGAATCCCATTCTTTTATGTCAGAATAATTCACTTTCCTTTCCTCATCAATTTCTTTTCTTTTGTTTTACAATATTCTTTGAAAACTATAATGAAATAATAATTTTAAAAAACAAAAACAAAACAGCTGCAAAGCCAACACAATAATAACTCACACACATAGCAATTAATATGCATTGAAGAAAACT... |
Task1_train_45569 | Chromosome 17 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GTGTAATTTGGTCATGTCACTCCTTCCCCAAAAGCTGTTGTCATCTTTCTCTGGATGTGTTCACTGAAAAGTCTACATACTTGCCTTTAGTTCCGTTCATTGTTTTTGTTAAGAAAGATTTTTTTTGAATCCCATTCTTTTATGTCAGAATAATTCACTTTCCTTTCCTCATCAATTTCTTTTCTTTTGTTTTACAATATTCTTTGAAAACTATAATGAAATAATAATTTTAAAAAACAAAAACAAAACAGCTGCAAAGCCAACACAATAATAACTCACACACATAGCAATTAATATGCATTGAAGAAAACTTAGCAAAC... | GTGTAATTTGGTCATGTCACTCCTTCCCCAAAAGCTGTTGTCATCTTTCTCTGGATGTGTTCACTGAAAAGTCTACATACTTGCCTTTAGTTCCGTTCATTGTTTTTGTTAAGAAAGATTTTTTTTGAATCCCATTCTTTTATGTCAGAATAATTCACTTTCCTTTCCTCATCAATTTCTTTTCTTTTGTTTTACAATATTCTTTGAAAACTATAATGAAATAATAATTTTAAAAAACAAAAACAAAACAGCTGCAAAGCCAACACAATAATAACTCACACACATAGCAATTAATATGCATTGAAGAAAACTTAGCAAAC... |
Task1_train_45570 | Located on Chromosome 17, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | AAAGATGAAACATGCAGCGAATTCAGACTAGACAAAAAAGGGGTGTGTGTAGGGATGACAGGCACGGAAACCAAACTATTGGATAGAGTATATAATTCAGAACGTAGAAAATGATATTGGGTAAGATGCTGTTTATAAAAATACTAAGTTCAGAAATATTTATGAGAATGCAGTAGGAACAAAGAAAATTAGGAGAATTTACTAAAAAGCTTGATAATCATGACATACTCCCTATAGGTACAAGATGACAGAATTCAGAAACTTCCCAAAAATAATTTTAAAATATATTGAAGATTTGGAATGTTTCTTTTTTTCCTCCA... | AAAGATGAAACATGCAGCGAATTCAGACTAGACAAAAAAGGGGTGTGTGTAGGGATGACAGGCACGGAAACCAAACTATTGGATAGAGTATATAATTCAGAACGTAGAAAATGATATTGGGTAAGATGCTGTTTATAAAAATACTAAGTTCAGAAATATTTATGAGAATGCAGTAGGAACAAAGAAAATTAGGAGAATTTACTAAAAAGCTTGATAATCATGACATACTCCCTATAGGTACAAGATGACAGAATTCAGAAACTTCCCAAAAATAATTTTAAAATATATTGAAGATTTGGAATGTTTCTTTTTTTCCTCCA... |
Task1_train_45571 | This genomic variant is located on Chromosome 17. Can you determine its pathogenicity and name any linked disease? | Benign | CAGGCTGGAGTGCAATAGCGCTATCTCAGCTCACCGCAACCTTGGCCTCCCGGCCGGGTTCAAGCAATTCTCCTGCCTCAGTCTCCCGAGGAGCTGGAATTACAGGCATTCACCACCACGCCTGGCTAATTTTGTATTTTTGGTAGAGATGGTGCTTCTCCATGTTGGTCAGATTGGTCTCTAACTCCTGACCTCAGGTGATCTGCCTGCCTCAGCCTCCCAAAGTTCTGGGATTACAGGCAGGAGCCACCGTGCCCGGACCTCATTTGCATTTTTAAGGACTGTTCTTGCTGCAGTGTGAGGCAAGAGTGGAAATGGAA... | CAGGCTGGAGTGCAATAGCGCTATCTCAGCTCACCGCAACCTTGGCCTCCCGGCCGGGTTCAAGCAATTCTCCTGCCTCAGTCTCCCGAGGAGCTGGAATTACAGGCATTCACCACCACGCCTGGCTAATTTTGTATTTTTGGTAGAGATGGTGCTTCTCCATGTTGGTCAGATTGGTCTCTAACTCCTGACCTCAGGTGATCTGCCTGCCTCAGCCTCCCAAAGTTCTGGGATTACAGGCAGGAGCCACCGTGCCCGGACCTCATTTGCATTTTTAAGGACTGTTCTTGCTGCAGTGTGAGGCAAGAGTGGAAATGGAA... |
Task1_train_45572 | With a mutation on Chromosome 17, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CTGCACTCCAGCATGGGTGACAGAGCGAGACTTCTCAAAAAAAAAAAAAAAAAAAGGAAAGAAAGAAAGGAAAGATTGTACATCGACTATGCAATTATAATATTTTTACTAATAACCCACTATTGTATATCAAGTGAGTTAAATGGGAAAGCACTTAGAGATTTCTAAGATCAAGTATCAAGCACCAGCATTCTTCATCTAGTTCTGACATAAACACTAATAGTATCATCATCCATAATCTCTCACAAGTGTCTCTTTTTAAAAAGAAACACTCTGGAGTGTTATAGCAGAGCCAAGTCTTAGAAAGTGATTCTATAAAC... | CTGCACTCCAGCATGGGTGACAGAGCGAGACTTCTCAAAAAAAAAAAAAAAAAAAGGAAAGAAAGAAAGGAAAGATTGTACATCGACTATGCAATTATAATATTTTTACTAATAACCCACTATTGTATATCAAGTGAGTTAAATGGGAAAGCACTTAGAGATTTCTAAGATCAAGTATCAAGCACCAGCATTCTTCATCTAGTTCTGACATAAACACTAATAGTATCATCATCCATAATCTCTCACAAGTGTCTCTTTTTAAAAAGAAACACTCTGGAGTGTTATAGCAGAGCCAAGTCTTAGAAAGTGATTCTATAAAC... |
Task1_train_45573 | A mutation on Chromosome 17 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CACTTTGGGAGGCCGAGGCAGGTGGATCACTTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATAGTGAAACTCTTTCTCTACTAAAAGTACAAAGATTAGCCGGGCATGGTGGCACTCGCCTGTAGTCACAACTACTAGGGAGGTTGAGGCAGAAGAATCACTTGAACCCGGGAGGGGGAGGTTGCAGTGAGCCAAGATCACGCCACTGCACTCCAGCCTGGGTGACGGAGCAAGACTCTGTCTCAAAAAAATAAAAAAAAAGAAAGAAATTATCTATCTATCTATCTATCTATCTATCTATCTTGACCAAATTTTT... | CACTTTGGGAGGCCGAGGCAGGTGGATCACTTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATAGTGAAACTCTTTCTCTACTAAAAGTACAAAGATTAGCCGGGCATGGTGGCACTCGCCTGTAGTCACAACTACTAGGGAGGTTGAGGCAGAAGAATCACTTGAACCCGGGAGGGGGAGGTTGCAGTGAGCCAAGATCACGCCACTGCACTCCAGCCTGGGTGACGGAGCAAGACTCTGTCTCAAAAAAATAAAAAAAAAGAAAGAAATTATCTATCTATCTATCTATCTATCTATCTATCTTGACCAAATTTTT... |
Task1_train_45574 | Here’s a variant located on Chromosome 17. What is the predicted biological effect — harmless or disease-causing? | Benign | GAGATTGGTTCTATTGATACCTGCTGAAACTTGTCCATGGGAATAATGGATTCATAAGCGATTCTCTACATTTGTATAAAATTACCATAACAAAGTTTTTGTTAAAGTTGGAAAAGTATCGGACAGTGACCAATATGAAACTAGATTGAAGATTTTATTATTCCAAAGGGTAAATCCTAGATGGGAAAAGTAAGTAAAAGAATAAACCCGAGAAAAACTGGAGGAACAAATTTGACAGGTCACATTAAAAAGGAAAAAAAACAAACAGGAAAATTGTGTCAGGAAGTTAATAGTCTCCCAGGAAACAAAGTAGAAGGGAA... | GAGATTGGTTCTATTGATACCTGCTGAAACTTGTCCATGGGAATAATGGATTCATAAGCGATTCTCTACATTTGTATAAAATTACCATAACAAAGTTTTTGTTAAAGTTGGAAAAGTATCGGACAGTGACCAATATGAAACTAGATTGAAGATTTTATTATTCCAAAGGGTAAATCCTAGATGGGAAAAGTAAGTAAAAGAATAAACCCGAGAAAAACTGGAGGAACAAATTTGACAGGTCACATTAAAAAGGAAAAAAAACAAACAGGAAAATTGTGTCAGGAAGTTAATAGTCTCCCAGGAAACAAAGTAGAAGGGAA... |
Task1_train_45575 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | TGACCCTGAAGAAGAAAGCAGATGAGAACGTCTGACCGTGAAATACGAGCTGAGAAAAATTCACAGCCTAGAGCACACCAGAGCAAGCAGCTGAAGGTAAAACCAATTTCCAGGATACCTGAACTCAGAGTGGATGAATGCAAGGGGGTAAGGTATGCTCTGAAGCTATAGTCAGGGTCGTGACGTATACCTGGGAAAAGATGACCCGTCAGGCCCCTCCCCACGTTCCACACAGAACACACAGTAGCCGCAGTTGTCCCCAGGGTAACAGTCCCATATTTACTTACTGAGAGACCTTATCTGAGGAGCACAGCTGGGCA... | TGACCCTGAAGAAGAAAGCAGATGAGAACGTCTGACCGTGAAATACGAGCTGAGAAAAATTCACAGCCTAGAGCACACCAGAGCAAGCAGCTGAAGGTAAAACCAATTTCCAGGATACCTGAACTCAGAGTGGATGAATGCAAGGGGGTAAGGTATGCTCTGAAGCTATAGTCAGGGTCGTGACGTATACCTGGGAAAAGATGACCCGTCAGGCCCCTCCCCACGTTCCACACAGAACACACAGTAGCCGCAGTTGTCCCCAGGGTAACAGTCCCATATTTACTTACTGAGAGACCTTATCTGAGGAGCACAGCTGGGCA... |
Task1_train_45576 | This sequence change occurs on Chromosome 17. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | ACTCAGCCACGCCGAACTGTGAGTCAATTAGATCTCTTTCCTTTATATATTACCCAGTCTCGGGTATGTCATTAGCAGCATGAGAACAGACTAATATATACACTTTTTTGTTAGCCACAGTTATCATTACTTTCTGCCCCTAGATTCTCTCCTTGTTGATACTGGCTTCTGAAATTATTTGCCTTTTTGCCCTATGAAAGAATGAAAACATATTTCAGAATTCTATGGATCAGCTGAGGAAAATGTGGGTAGGAAGCAGGTAGAGGTTTAGGCTGCACAGAACAGCTACCTAGAAAAGTGGCACATGAAGTAGTCTTGCT... | ACTCAGCCACGCCGAACTGTGAGTCAATTAGATCTCTTTCCTTTATATATTACCCAGTCTCGGGTATGTCATTAGCAGCATGAGAACAGACTAATATATACACTTTTTTGTTAGCCACAGTTATCATTACTTTCTGCCCCTAGATTCTCTCCTTGTTGATACTGGCTTCTGAAATTATTTGCCTTTTTGCCCTATGAAAGAATGAAAACATATTTCAGAATTCTATGGATCAGCTGAGGAAAATGTGGGTAGGAAGCAGGTAGAGGTTTAGGCTGCACAGAACAGCTACCTAGAAAAGTGGCACATGAAGTAGTCTTGCT... |
Task1_train_45577 | This variant is present on Chromosome 17. Is the change likely to result in a pathogenic outcome? | Benign | AATTCTGAAACACTGTTGATGTAAAACTAAATTGATGCAACCACTTTGGGAAAATATTTGGTGGTAGCTACTAAGATTAATATTTGTATACTCTCAGCCCCACTATTCTGTTTGTTATATTAACGTAATGAACAGAATGAAATGTCCATATTCAGTAGGAAATGTGTACTAGAATGTTTGTAGCAGCTTTATTAAAAATGCTCAAAAACTAAAAATTATCATAATCTATTGATAAGAAAATTGATAGTATGTTAACACAATAGGATGCTACATAACTCTACACTATAGCTACACAGAAACTATGCTGCCACCTAAAAACG... | AATTCTGAAACACTGTTGATGTAAAACTAAATTGATGCAACCACTTTGGGAAAATATTTGGTGGTAGCTACTAAGATTAATATTTGTATACTCTCAGCCCCACTATTCTGTTTGTTATATTAACGTAATGAACAGAATGAAATGTCCATATTCAGTAGGAAATGTGTACTAGAATGTTTGTAGCAGCTTTATTAAAAATGCTCAAAAACTAAAAATTATCATAATCTATTGATAAGAAAATTGATAGTATGTTAACACAATAGGATGCTACATAACTCTACACTATAGCTACACAGAAACTATGCTGCCACCTAAAAACG... |
Task1_train_45578 | A variant on Chromosome 17 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TAATCTCCAAGCCATTCCACCATTTACACACATATATGAATGCACACACACACACCATTCACCTTTTCTGAGGTCTAAAACACTCACTGAAAATAACTGTTTAGTTTTTGTAACGCATCCTAGCAATCCTCAAACAGGTTGTTTTGTGATGAATAAGTCCACTCTGCCTTTCTCTTCCGGTTTAGACTAGCACAAAACTAATTGATGCTAATACTGGAAAACACTCATACTTGTCACTCAAACCGAAAACATCCTTTACCTTTCCTGCCAAGCAGCCTGTGGGAAAAGCTTCAAAATCTCTGTGTGGAGAGCTTCCACCT... | TAATCTCCAAGCCATTCCACCATTTACACACATATATGAATGCACACACACACACCATTCACCTTTTCTGAGGTCTAAAACACTCACTGAAAATAACTGTTTAGTTTTTGTAACGCATCCTAGCAATCCTCAAACAGGTTGTTTTGTGATGAATAAGTCCACTCTGCCTTTCTCTTCCGGTTTAGACTAGCACAAAACTAATTGATGCTAATACTGGAAAACACTCATACTTGTCACTCAAACCGAAAACATCCTTTACCTTTCCTGCCAAGCAGCCTGTGGGAAAAGCTTCAAAATCTCTGTGTGGAGAGCTTCCACCT... |
Task1_train_45579 | Given this variant on Chromosome 17, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GGTAGAAAAAGCAAGTATTAAAATAAAAAAATTTTAAAGACAGGACTATTACAGATTATCTGCTTGCAGTTCCCATCTTGCAGAAGAGAAAGCTGTGCCATAATGGTAACAAACGGTGCACAGCATAACCAGTTATCCAGTCTACCCACTCATTCATCCATTCAACAAATATTTATAGAGCTTCTGCTCCGTGCAATGCATCATCCTTTGTGCTAGAAATAAGTCAAGTATAATTATTACTTTCAAGAAGTTCATATTTGAAAAACAATGACAAACTGAGTCTGAACTCAGTTCCACTGAAAAATAAATTAGGAGGGTCT... | GGTAGAAAAAGCAAGTATTAAAATAAAAAAATTTTAAAGACAGGACTATTACAGATTATCTGCTTGCAGTTCCCATCTTGCAGAAGAGAAAGCTGTGCCATAATGGTAACAAACGGTGCACAGCATAACCAGTTATCCAGTCTACCCACTCATTCATCCATTCAACAAATATTTATAGAGCTTCTGCTCCGTGCAATGCATCATCCTTTGTGCTAGAAATAAGTCAAGTATAATTATTACTTTCAAGAAGTTCATATTTGAAAAACAATGACAAACTGAGTCTGAACTCAGTTCCACTGAAAAATAAATTAGGAGGGTCT... |
Task1_train_45580 | This mutation is located on Chromosome 17. Is it associated with a disease or is it a benign polymorphism? | Benign | TCTATTCCCACCCCTTTACCTTAAGTTTATGTGAGTCCTTATGTGTTGGGTGAGTCTCTTGAAGACAGCAGATACTTGGTTGGTGAATTTTTATTCATTCTGCTATTCTGTATCTTTTAAGTGGCACATTTAGGCCATTTACATTCAATGTGGGTATTGAGATGTGAGGTACTATGCTATTCATCATGCTGGTTTTCTAGAATGCTGGTTATGCTAGCAGTGAAGTTGCCACGTGGACAGACTCAGGACCTCTGGTTAGCCAGGGTGTTGCAAGTGGTAGAATTATCTGTTGTTTTCTCCTTCTTTGGTGCAGGATTGTT... | TCTATTCCCACCCCTTTACCTTAAGTTTATGTGAGTCCTTATGTGTTGGGTGAGTCTCTTGAAGACAGCAGATACTTGGTTGGTGAATTTTTATTCATTCTGCTATTCTGTATCTTTTAAGTGGCACATTTAGGCCATTTACATTCAATGTGGGTATTGAGATGTGAGGTACTATGCTATTCATCATGCTGGTTTTCTAGAATGCTGGTTATGCTAGCAGTGAAGTTGCCACGTGGACAGACTCAGGACCTCTGGTTAGCCAGGGTGTTGCAAGTGGTAGAATTATCTGTTGTTTTCTCCTTCTTTGGTGCAGGATTGTT... |
Task1_train_45581 | Here is a variant on Chromosome 17. Please identify whether it is a benign mutation or associated with a disorder. | Benign | ATATGTCAGTGTTGTTGAAAATTGTAAGTTGTAAAATCTTGTGTAATAGTTATGGATACAGACATATGTAGTAACATCAAAAAAACACGTATGGGAATTACAAATTGTGAAATTGTGAATTGCGGTTACTCCTACGGAGGAGAGAAGGAAACAAGATTGGAGAGGGGTAACATGAGTTTTCACCTGTGTCTTAAAAGTTTTACTAAAAACAAATATTATGCAATATTAACATTTGAAATATTTGGATAGTAGGTGGTTCGTTTTCTGTACGTTTGAAATATTTCATAATATGAGATACCTCTCCACAGACACTGCTGCTG... | ATATGTCAGTGTTGTTGAAAATTGTAAGTTGTAAAATCTTGTGTAATAGTTATGGATACAGACATATGTAGTAACATCAAAAAAACACGTATGGGAATTACAAATTGTGAAATTGTGAATTGCGGTTACTCCTACGGAGGAGAGAAGGAAACAAGATTGGAGAGGGGTAACATGAGTTTTCACCTGTGTCTTAAAAGTTTTACTAAAAACAAATATTATGCAATATTAACATTTGAAATATTTGGATAGTAGGTGGTTCGTTTTCTGTACGTTTGAAATATTTCATAATATGAGATACCTCTCCACAGACACTGCTGCTG... |
Task1_train_45582 | This is a variant located on Chromosome 17. Is this mutation a likely cause of disease or not? | Benign | ATACTTAACTAGTTGTACCAATAACTTACATTGGAGGTTATATATAATCTCCAATGTTGAATAAAAAGACGTGAAAAGCACTGTAACCATAAAAGAACAGATTCATAAATTGGACTTCATTCAAATTAAGACTTGTGTTTGTCAAAAGACACTGCTAGTAGAATTAAAAGGCAAGCCTCAGACTGAGATCAAATATTTAAATACCTGTATCTAACAAAGGTCTTGAAACAAAAATGTGAAAAGAACTTGAATAGGCATTTCATAAAGGAAAACCTCCAAATGCCAATAATCATATAAAAAGGTGATTAATAACATTAGTT... | ATACTTAACTAGTTGTACCAATAACTTACATTGGAGGTTATATATAATCTCCAATGTTGAATAAAAAGACGTGAAAAGCACTGTAACCATAAAAGAACAGATTCATAAATTGGACTTCATTCAAATTAAGACTTGTGTTTGTCAAAAGACACTGCTAGTAGAATTAAAAGGCAAGCCTCAGACTGAGATCAAATATTTAAATACCTGTATCTAACAAAGGTCTTGAAACAAAAATGTGAAAAGAACTTGAATAGGCATTTCATAAAGGAAAACCTCCAAATGCCAATAATCATATAAAAAGGTGATTAATAACATTAGTT... |
Task1_train_45583 | The following genetic variant occurs on Chromosome 17. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GGAAAAAAAGTCCATATACCACATATACAGACTTTAATCACTATAACTAAATTTTTAATATTATATATATGCTATATTATGGAAGAACTGTAACAAGCAATTAATTTCTAATGTTCCAAGATTTCACATTTCCTGAACTCTGAAATACACAGAAATATACGTGGAGTATATTGAAATACACTGAAATATACACGGAGTGTGCCCATGATTCAAATAAAATGTGAAATAAAATTTAAACACGTATTGTCAACACAAGCTTTGACATTCTTCATCCCTTATGTTAAATGAAGCCAATTAGTTGTTGAAACTTCTTGACTAAT... | GGAAAAAAAGTCCATATACCACATATACAGACTTTAATCACTATAACTAAATTTTTAATATTATATATATGCTATATTATGGAAGAACTGTAACAAGCAATTAATTTCTAATGTTCCAAGATTTCACATTTCCTGAACTCTGAAATACACAGAAATATACGTGGAGTATATTGAAATACACTGAAATATACACGGAGTGTGCCCATGATTCAAATAAAATGTGAAATAAAATTTAAACACGTATTGTCAACACAAGCTTTGACATTCTTCATCCCTTATGTTAAATGAAGCCAATTAGTTGTTGAAACTTCTTGACTAAT... |
Task1_train_45584 | Located on Chromosome 17, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | CTTGCAAGGCCGTAGAATTTGTCCACAGAAAATCATCACCAGTCATCACTGAGCATTTGTCACAGTAGGTTTTATTAAGTTCAGACAGATTCAATTATAATTAAATCAATCAACCTTTCATATATTGGCTAACAGACAGACTTCTAAGAAAACCAAGCTTCCCTAAAAAAAAGCAATTAGATATTATTTTCTTGATTCAACTTATGTGAGCATATGAATAATTTACTTTTGTTTGTTTAATTCACAAATAGCTCAATTTATAAGTATTGGTGTGGGCTATAGGCTTAAGAAACATGTTTGTGTAAAGCTGCTGTCCCACG... | CTTGCAAGGCCGTAGAATTTGTCCACAGAAAATCATCACCAGTCATCACTGAGCATTTGTCACAGTAGGTTTTATTAAGTTCAGACAGATTCAATTATAATTAAATCAATCAACCTTTCATATATTGGCTAACAGACAGACTTCTAAGAAAACCAAGCTTCCCTAAAAAAAAGCAATTAGATATTATTTTCTTGATTCAACTTATGTGAGCATATGAATAATTTACTTTTGTTTGTTTAATTCACAAATAGCTCAATTTATAAGTATTGGTGTGGGCTATAGGCTTAAGAAACATGTTTGTGTAAAGCTGCTGTCCCACG... |
Task1_train_45585 | A variant was discovered on Chromosome 17. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | ACAAGAAAATAATTGTATCTCTATATCTGCTTTTTAATTTGAAATCATATGGACCTTTGATTATACTTCATCCCATTCTCATGCCTCCTATGACCAGTTGAGAGGGTGGACACTGAGAATCCTACAGCAGCTTCTTCTGTTTGTAAAATATTGTTCAATGACAAGTCAGACAGATAGAAACCTCCAAAGCATGGTGGCTATTGTGGACAAAATTTGTGAAAATATTTTACATTGGACCTTCCAGTAAGCATTTTCGCAGCCCTAGGTCACATCTTGAAATTATACAATTGGATCCCCCCAAATTGGGTTGAAGTGCTGAC... | ACAAGAAAATAATTGTATCTCTATATCTGCTTTTTAATTTGAAATCATATGGACCTTTGATTATACTTCATCCCATTCTCATGCCTCCTATGACCAGTTGAGAGGGTGGACACTGAGAATCCTACAGCAGCTTCTTCTGTTTGTAAAATATTGTTCAATGACAAGTCAGACAGATAGAAACCTCCAAAGCATGGTGGCTATTGTGGACAAAATTTGTGAAAATATTTTACATTGGACCTTCCAGTAAGCATTTTCGCAGCCCTAGGTCACATCTTGAAATTATACAATTGGATCCCCCCAAATTGGGTTGAAGTGCTGAC... |
Task1_train_45586 | This genomic variant is located on Chromosome 17. Can you determine its pathogenicity and name any linked disease? | Benign | CCGAACAAACCCACACTCTGTCTGTCTCTTCTTTCCACAGGGCTCACTGTGAGTTCACAGTTGTCCTCATCCCCTTTCCTTCAATAATGTCAATCTTTGCCTTTAAAAAAAAAAAAAAAAAAAGCCAGACTAGCCAATTTCCTTCCCTTTTTCTGTGTCCCCCTCCCATGTAGTATCTCCTTAGGGGGAGGTAAAGGAAGACATGCTCCTCTCTGGGCTGGCTCGGCCTTGGAAGGTAGCTTGCTATCTTTATGATGCTCCAGTTCCAACATTCTAGATGGGGAGAGGCTCAGCAGTGATGGAGCAGGAGGGGCGGATGA... | CCGAACAAACCCACACTCTGTCTGTCTCTTCTTTCCACAGGGCTCACTGTGAGTTCACAGTTGTCCTCATCCCCTTTCCTTCAATAATGTCAATCTTTGCCTTTAAAAAAAAAAAAAAAAAAAGCCAGACTAGCCAATTTCCTTCCCTTTTTCTGTGTCCCCCTCCCATGTAGTATCTCCTTAGGGGGAGGTAAAGGAAGACATGCTCCTCTCTGGGCTGGCTCGGCCTTGGAAGGTAGCTTGCTATCTTTATGATGCTCCAGTTCCAACATTCTAGATGGGGAGAGGCTCAGCAGTGATGGAGCAGGAGGGGCGGATGA... |
Task1_train_45587 | This sequence variant lies on Chromosome 17. Is it clinically significant, and what condition might it cause if any? | Benign | TTCTTTTTGCCATTTTTGAGGTGATACATTTACTTTTCGAATGACTTCCGTTGAATAATGTTATTTGTTCCATCAGTCCTGGGGAGTGAAGAAAGTGGGTCGTAAAAGTCTGCCAGACACAGACGAAGCCAGACCAAGATGGAACCTTGTGGGCAATCTCAGGTTAGCAGGTAATCAGATCATTCACCCATCTGTCCATCTGTTTATCCAATTCAACCCAGAGATTCACAAGCACCAGGCTCCATGATGGCATATTTTGCAGGCAAATGGCTATTAAGTTCTTCATTCTCCTCCACGTGTTCTGGAAAATCACCAGGTTT... | TTCTTTTTGCCATTTTTGAGGTGATACATTTACTTTTCGAATGACTTCCGTTGAATAATGTTATTTGTTCCATCAGTCCTGGGGAGTGAAGAAAGTGGGTCGTAAAAGTCTGCCAGACACAGACGAAGCCAGACCAAGATGGAACCTTGTGGGCAATCTCAGGTTAGCAGGTAATCAGATCATTCACCCATCTGTCCATCTGTTTATCCAATTCAACCCAGAGATTCACAAGCACCAGGCTCCATGATGGCATATTTTGCAGGCAAATGGCTATTAAGTTCTTCATTCTCCTCCACGTGTTCTGGAAAATCACCAGGTTT... |
Task1_train_45588 | A genomic change on Chromosome 17 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GTCCTGGGGAGTGAAGAAAGTGGGTCGTAAAAGTCTGCCAGACACAGACGAAGCCAGACCAAGATGGAACCTTGTGGGCAATCTCAGGTTAGCAGGTAATCAGATCATTCACCCATCTGTCCATCTGTTTATCCAATTCAACCCAGAGATTCACAAGCACCAGGCTCCATGATGGCATATTTTGCAGGCAAATGGCTATTAAGTTCTTCATTCTCCTCCACGTGTTCTGGAAAATCACCAGGTTTCCAGGTAACGACGGGATTGTATTTGTCAGCACAGAACTGGGGATGTGGAGGACAAAGTCTCCAAGGAGTAGTTCT... | GTCCTGGGGAGTGAAGAAAGTGGGTCGTAAAAGTCTGCCAGACACAGACGAAGCCAGACCAAGATGGAACCTTGTGGGCAATCTCAGGTTAGCAGGTAATCAGATCATTCACCCATCTGTCCATCTGTTTATCCAATTCAACCCAGAGATTCACAAGCACCAGGCTCCATGATGGCATATTTTGCAGGCAAATGGCTATTAAGTTCTTCATTCTCCTCCACGTGTTCTGGAAAATCACCAGGTTTCCAGGTAACGACGGGATTGTATTTGTCAGCACAGAACTGGGGATGTGGAGGACAAAGTCTCCAAGGAGTAGTTCT... |
Task1_train_45589 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | ATACAAAGTACGGAAGAAATATTTTGGTGACTATTACATGAGACAAAGTCTGCTGATCTACTGTCAAATACAATTCGTTTTTCCTTTACTTTGAGGTCATTTAGTCAATAGTTTTTAAGACTCCTTCTTAAGGCAATCTTTCAGAAATGTAGAAGAGTACAGAGAATAACAAGATGTAAGTCCACGTACCAACGATCTAGATTTAATAAAGGTTAACCTGTTACCATATTTGATTCAGATTTTTTAAGTAAACTATTACAGAAAGAATTGCAGCTCTTCTCTCTCCGCACCAATTAGAGGTACTCAATATCTGAAAAATT... | ATACAAAGTACGGAAGAAATATTTTGGTGACTATTACATGAGACAAAGTCTGCTGATCTACTGTCAAATACAATTCGTTTTTCCTTTACTTTGAGGTCATTTAGTCAATAGTTTTTAAGACTCCTTCTTAAGGCAATCTTTCAGAAATGTAGAAGAGTACAGAGAATAACAAGATGTAAGTCCACGTACCAACGATCTAGATTTAATAAAGGTTAACCTGTTACCATATTTGATTCAGATTTTTTAAGTAAACTATTACAGAAAGAATTGCAGCTCTTCTCTCTCCGCACCAATTAGAGGTACTCAATATCTGAAAAATT... |
Task1_train_45590 | A mutation has occurred on Chromosome 17. What is the medical relevance of this mutation? | Benign | TTTTTTGAGACAGGATCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCACCCGCGTAGCTGGGATTACAGGCACCTGCCACCATGTCCGACTAATTTTTGTACTTTCAGTAGAGACGGGGTTTCACCATATTGGCCCGGCTGGTCTCCAACCCCTGACCTCATGTGATCTGCCTGCCTTGGCCTCCCAAAGTGATGGGATTACAGGCGCGAGAGCCACCGCGCACGGCCCCTTAAAGAATATAGACCTAGCAATGAACG... | TTTTTTGAGACAGGATCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCACCCGCGTAGCTGGGATTACAGGCACCTGCCACCATGTCCGACTAATTTTTGTACTTTCAGTAGAGACGGGGTTTCACCATATTGGCCCGGCTGGTCTCCAACCCCTGACCTCATGTGATCTGCCTGCCTTGGCCTCCCAAAGTGATGGGATTACAGGCGCGAGAGCCACCGCGCACGGCCCCTTAAAGAATATAGACCTAGCAATGAACG... |
Task1_train_45591 | A mutation on Chromosome 17 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GGCCTCCCAGAGTTGCGCAGTGCAGGCCTGTCCCCTTCTTGACAGGTCACCTCTGAAGAGCTATGAACGACTCAGTTAATCAGGATAAGCAGTCATCGATTCTTTCCTTCCATCTTCGGGGGAGGTAGGAGGATTGAGAGGAAAGGGAAGCCATTACCTTTTGCTTTTTTGACAACTTAAGTTCTACTTTGAAAACCCCCAGGACTGCATAGCACTCATTTCTTCTTTCTACTCTTTTGATCCCCGTTTTTGTTTCCTCCCGATCTTTGCCATTCTTCTCAACCAACAGAATGACCAGAGTTGTGGGGCGGCTGCCACAC... | GGCCTCCCAGAGTTGCGCAGTGCAGGCCTGTCCCCTTCTTGACAGGTCACCTCTGAAGAGCTATGAACGACTCAGTTAATCAGGATAAGCAGTCATCGATTCTTTCCTTCCATCTTCGGGGGAGGTAGGAGGATTGAGAGGAAAGGGAAGCCATTACCTTTTGCTTTTTTGACAACTTAAGTTCTACTTTGAAAACCCCCAGGACTGCATAGCACTCATTTCTTCTTTCTACTCTTTTGATCCCCGTTTTTGTTTCCTCCCGATCTTTGCCATTCTTCTCAACCAACAGAATGACCAGAGTTGTGGGGCGGCTGCCACAC... |
Task1_train_45592 | This alteration on Chromosome 17 may affect genome function. Does it lead to a disease or is it benign? | Benign | TTGACATTTTCTTGTTAATACACGTTTCATTTCAGTACGATGCCAACTGTTAAGCCTGCAGGAATCCTCCTGGGTATTTCTGAATTGTGCTGTGTGCATGTGTGTTTGAAAGCTCAAACAGCTTGTCTTCTTACAGCATCGAGTTGTTTGCTTTATTGTTAGACACAATATTAGCAGTGTATCCTTTCCGTATTCCCTACCATCGAACCCATTAAGATCTAAAATCCTTGTCAAGTATCTGGCTTTAAAAGTTGGGAGATGGTAGTTTAAAAAAAAAAAAAGCTCTTGCAAAAACCATCCAGTCCCTAAGCATGGGCTAT... | TTGACATTTTCTTGTTAATACACGTTTCATTTCAGTACGATGCCAACTGTTAAGCCTGCAGGAATCCTCCTGGGTATTTCTGAATTGTGCTGTGTGCATGTGTGTTTGAAAGCTCAAACAGCTTGTCTTCTTACAGCATCGAGTTGTTTGCTTTATTGTTAGACACAATATTAGCAGTGTATCCTTTCCGTATTCCCTACCATCGAACCCATTAAGATCTAAAATCCTTGTCAAGTATCTGGCTTTAAAAGTTGGGAGATGGTAGTTTAAAAAAAAAAAAAGCTCTTGCAAAAACCATCCAGTCCCTAAGCATGGGCTAT... |
Task1_train_45593 | A mutation on Chromosome 17 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCTGGCGTGGTGGCGCATGCCTGTAGTCCCAGCTCCTCGGGATGCTGAGGCAGGACAATAGCTTGAACCTGGGAAATGGAGGTTTCAGTGAGCCGACACTGCACTCCGGCCTGGTGACAGAGTGAGACTCTGTCTCAAAAAAAAAAAAAAAAAAGTATAAGTGAAAAACAGGACTGTGTCCTTGGCCATGTATATATTTGTGCATTATGCATACATTTTATGTATATCTGTGTGTGTGTGTGTGTGTATATGCATATTACTAAATGTTAGTAGA... | GGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCTGGCGTGGTGGCGCATGCCTGTAGTCCCAGCTCCTCGGGATGCTGAGGCAGGACAATAGCTTGAACCTGGGAAATGGAGGTTTCAGTGAGCCGACACTGCACTCCGGCCTGGTGACAGAGTGAGACTCTGTCTCAAAAAAAAAAAAAAAAAAGTATAAGTGAAAAACAGGACTGTGTCCTTGGCCATGTATATATTTGTGCATTATGCATACATTTTATGTATATCTGTGTGTGTGTGTGTGTGTATATGCATATTACTAAATGTTAGTAGA... |
Task1_train_45594 | A sequence alteration has been identified on Chromosome 17. Is it disease-inducing or harmless? | Benign | AATGGAGGTTTCAGTGAGCCGACACTGCACTCCGGCCTGGTGACAGAGTGAGACTCTGTCTCAAAAAAAAAAAAAAAAAAGTATAAGTGAAAAACAGGACTGTGTCCTTGGCCATGTATATATTTGTGCATTATGCATACATTTTATGTATATCTGTGTGTGTGTGTGTGTGTATATGCATATTACTAAATGTTAGTAGAGCTTCATTTCTCATTCTTTGATTGTGGTAATTCTAATATTTTCTTCTTACACCCTAGTGCATATTCTATTTATCACTTTGGAAACCTCTGCTGTAATCAGTAACCTTTGGCTGGGCGTGG... | AATGGAGGTTTCAGTGAGCCGACACTGCACTCCGGCCTGGTGACAGAGTGAGACTCTGTCTCAAAAAAAAAAAAAAAAAAGTATAAGTGAAAAACAGGACTGTGTCCTTGGCCATGTATATATTTGTGCATTATGCATACATTTTATGTATATCTGTGTGTGTGTGTGTGTGTATATGCATATTACTAAATGTTAGTAGAGCTTCATTTCTCATTCTTTGATTGTGGTAATTCTAATATTTTCTTCTTACACCCTAGTGCATATTCTATTTATCACTTTGGAAACCTCTGCTGTAATCAGTAACCTTTGGCTGGGCGTGG... |
Task1_train_45595 | A mutation located on Chromosome 17 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | AAAAAAGTATAAGTGAAAAACAGGACTGTGTCCTTGGCCATGTATATATTTGTGCATTATGCATACATTTTATGTATATCTGTGTGTGTGTGTGTGTGTATATGCATATTACTAAATGTTAGTAGAGCTTCATTTCTCATTCTTTGATTGTGGTAATTCTAATATTTTCTTCTTACACCCTAGTGCATATTCTATTTATCACTTTGGAAACCTCTGCTGTAATCAGTAACCTTTGGCTGGGCGTGGGCGTGGTAGCTCGCGCCTGTAATCTCAGCACTTTAGGGGGCTGAGGTGGGTGGATTGCCAGAGCTCAGGAGTTC... | AAAAAAGTATAAGTGAAAAACAGGACTGTGTCCTTGGCCATGTATATATTTGTGCATTATGCATACATTTTATGTATATCTGTGTGTGTGTGTGTGTGTATATGCATATTACTAAATGTTAGTAGAGCTTCATTTCTCATTCTTTGATTGTGGTAATTCTAATATTTTCTTCTTACACCCTAGTGCATATTCTATTTATCACTTTGGAAACCTCTGCTGTAATCAGTAACCTTTGGCTGGGCGTGGGCGTGGTAGCTCGCGCCTGTAATCTCAGCACTTTAGGGGGCTGAGGTGGGTGGATTGCCAGAGCTCAGGAGTTC... |
Task1_train_45596 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | AACTAATAAATGTTGTACTTAGTTTGGGACTTCTACATCAAGACAGTAAATAAGGTGTAATCATCATAGGGCCTCTACTTCTATTATAAACTGAAAAACTATTGAAGTTGGATCCAGGATCAGTGTTCAGACTTTGATGTTACCACCAAATGAACACAAGATACTAGAGGAGAGAGACCCTAGGATCAGGTCAAGCCCTGATCCCTCCATTGGCCAAGGACTTCAAGGCCATATCAATCTATAGGGATTAAAAGATGGTGCCATTGGCTCCTTAAAAAGCTTTGTAATTTCACCAGGCAATGACTGTCTCCAATGACTGC... | AACTAATAAATGTTGTACTTAGTTTGGGACTTCTACATCAAGACAGTAAATAAGGTGTAATCATCATAGGGCCTCTACTTCTATTATAAACTGAAAAACTATTGAAGTTGGATCCAGGATCAGTGTTCAGACTTTGATGTTACCACCAAATGAACACAAGATACTAGAGGAGAGAGACCCTAGGATCAGGTCAAGCCCTGATCCCTCCATTGGCCAAGGACTTCAAGGCCATATCAATCTATAGGGATTAAAAGATGGTGCCATTGGCTCCTTAAAAAGCTTTGTAATTTCACCAGGCAATGACTGTCTCCAATGACTGC... |
Task1_train_45597 | A mutation on Chromosome 17 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CAGAGCAAGACTCTGTCTCAAAAAACAAAAAACAAAAAAACAAAAAACAAAAAACAAAAGCCGGGCGCAGTGACTCATGCCTGTAATCCCAGCACTTCGGAAGGCCGAGGCAGGTGGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCTAACATGGTGAAACCCCGTTTCTACTAAAATTACAAAAAATTAGCTGGGCGTGGTAGTGTGCGCCGTTAATCCCAGCTACTCAGGAGGCCTCAGGCAGGAGAATCGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCTAAGATGGTGCCATTGCACTCCAGCTTAGG... | CAGAGCAAGACTCTGTCTCAAAAAACAAAAAACAAAAAAACAAAAAACAAAAAACAAAAGCCGGGCGCAGTGACTCATGCCTGTAATCCCAGCACTTCGGAAGGCCGAGGCAGGTGGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCTAACATGGTGAAACCCCGTTTCTACTAAAATTACAAAAAATTAGCTGGGCGTGGTAGTGTGCGCCGTTAATCCCAGCTACTCAGGAGGCCTCAGGCAGGAGAATCGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCTAAGATGGTGCCATTGCACTCCAGCTTAGG... |
Task1_train_45598 | A variant affecting Chromosome 17 has been observed. Determine if it's benign or associated with disease. | Benign | GAGGCTGCAGCGGGGCAGGGGTGGCAAAGCTGCTATGAGCCAGGCCCCCCACTGTGCAGGGAGGAACTGCCCTGCTACCCTCTCCTCCAGGGCGCCTTCAGGGCTATCCATCCCACTGTCACCCGGTCAGTGTCCACATGAGGCTCTCTCACCCGAGTGTGGCTTAGGTTGTGTGACTGTGTTTCTGATGGGCTCTTATCTTCCTGCAGGGAGGACAGAGAAGCAGCATCCTTTCTTTATTGTGTATGTGACAAATCTATTACCCTGCCAAGGGAGTCAGGAGCCACAAAGGCTGTGTGTCTGACACACCGATAGCACCG... | GAGGCTGCAGCGGGGCAGGGGTGGCAAAGCTGCTATGAGCCAGGCCCCCCACTGTGCAGGGAGGAACTGCCCTGCTACCCTCTCCTCCAGGGCGCCTTCAGGGCTATCCATCCCACTGTCACCCGGTCAGTGTCCACATGAGGCTCTCTCACCCGAGTGTGGCTTAGGTTGTGTGACTGTGTTTCTGATGGGCTCTTATCTTCCTGCAGGGAGGACAGAGAAGCAGCATCCTTTCTTTATTGTGTATGTGACAAATCTATTACCCTGCCAAGGGAGTCAGGAGCCACAAAGGCTGTGTGTCTGACACACCGATAGCACCG... |
Task1_train_45599 | A mutation on Chromosome 17 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | AGGCTGCAGCGGGGCAGGGGTGGCAAAGCTGCTATGAGCCAGGCCCCCCACTGTGCAGGGAGGAACTGCCCTGCTACCCTCTCCTCCAGGGCGCCTTCAGGGCTATCCATCCCACTGTCACCCGGTCAGTGTCCACATGAGGCTCTCTCACCCGAGTGTGGCTTAGGTTGTGTGACTGTGTTTCTGATGGGCTCTTATCTTCCTGCAGGGAGGACAGAGAAGCAGCATCCTTTCTTTATTGTGTATGTGACAAATCTATTACCCTGCCAAGGGAGTCAGGAGCCACAAAGGCTGTGTGTCTGACACACCGATAGCACCGC... | AGGCTGCAGCGGGGCAGGGGTGGCAAAGCTGCTATGAGCCAGGCCCCCCACTGTGCAGGGAGGAACTGCCCTGCTACCCTCTCCTCCAGGGCGCCTTCAGGGCTATCCATCCCACTGTCACCCGGTCAGTGTCCACATGAGGCTCTCTCACCCGAGTGTGGCTTAGGTTGTGTGACTGTGTTTCTGATGGGCTCTTATCTTCCTGCAGGGAGGACAGAGAAGCAGCATCCTTTCTTTATTGTGTATGTGACAAATCTATTACCCTGCCAAGGGAGTCAGGAGCCACAAAGGCTGTGTGTCTGACACACCGATAGCACCGC... |
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