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_39100 | This genomic variant is located on Chromosome 9. Can you determine its pathogenicity and name any linked disease? | Benign | CTGAGCATGGTTGTGCATATCTGTAATCCCAGCAACTGGGAGGCAGAAGCAAGAGAACTGCTTGAACCTGGGAGACAGAGGTTGCAGTGAGCCGAGATGGTGCCACAGCACTCCAGCCTGGGTGACAGAGTGAGACTCTGTCTCAAAAAAAAAAAAAAAAAGAAATTGCAATATGGACTGTGGTTTAAATGATCATATCAGGCTGGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCAAGGGTGGTCAGATCACTTGAGGTCAGGCATTCGAGACCAGCCTGGCCAACATGTTGAAACCCCGTCTCTACT... | CTGAGCATGGTTGTGCATATCTGTAATCCCAGCAACTGGGAGGCAGAAGCAAGAGAACTGCTTGAACCTGGGAGACAGAGGTTGCAGTGAGCCGAGATGGTGCCACAGCACTCCAGCCTGGGTGACAGAGTGAGACTCTGTCTCAAAAAAAAAAAAAAAAAGAAATTGCAATATGGACTGTGGTTTAAATGATCATATCAGGCTGGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCAAGGGTGGTCAGATCACTTGAGGTCAGGCATTCGAGACCAGCCTGGCCAACATGTTGAAACCCCGTCTCTACT... |
Task1_train_39101 | Here is a variant on Chromosome 9. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TAACCACATCAGGGTGTGGCTTTCACAGAAGCTGAAGAAAGCCTGAAGCAGTGACTCAGTCGGGAGGAGGTGGGTTTAGAAGCCATCTGCTGTACTTCCTATACTTCTTGGTTTGGACTTTTGAACACTGAGACATTCTAGGCATAACACAGATATAAACTCATGGTGCCCAAAAGCATTTCAAAACCTTTTCTTTTCTTCATTCCTGCCTTCCTTTCCTTTCCTTCCTTTCCTTTCGTTCTTCCTTTTTTTCTGTGTCTCTGTCTCTCTTTCTCTCTTTTTCATTTTTGAGACAGGATCTTCCTCTGTTGCCCTAGAGT... | TAACCACATCAGGGTGTGGCTTTCACAGAAGCTGAAGAAAGCCTGAAGCAGTGACTCAGTCGGGAGGAGGTGGGTTTAGAAGCCATCTGCTGTACTTCCTATACTTCTTGGTTTGGACTTTTGAACACTGAGACATTCTAGGCATAACACAGATATAAACTCATGGTGCCCAAAAGCATTTCAAAACCTTTTCTTTTCTTCATTCCTGCCTTCCTTTCCTTTCCTTCCTTTCCTTTCGTTCTTCCTTTTTTTCTGTGTCTCTGTCTCTCTTTCTCTCTTTTTCATTTTTGAGACAGGATCTTCCTCTGTTGCCCTAGAGT... |
Task1_train_39102 | A mutation on Chromosome 9 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TAAGTTTGAAATGCATAGCCCAGGTCAGCGACAAGGTCTGCGCTTTGAAAGGTTCTTGTGTTTCCTCTTTTAAATGTCTGGTTTAGCCTTAAGTAGTATTTACTGAGTGCCACATGATCCAGTGGTTGGAGTATGTAGGTTTTGCCCTTATCTTCATTCTTTGCATCTGTTTGAACTCATGACAATACAAAACAAGGTGTTCCTGGGATAGGGAATGTTTTGTCCAAAAGGAGTCAACACGGAGAAAACTCTTCCTACAGTTAAGACAGGGTTTGGTTTTGTTTTTAAATGAGGAGAGAAACTGAGAAGTGGAAAACACA... | TAAGTTTGAAATGCATAGCCCAGGTCAGCGACAAGGTCTGCGCTTTGAAAGGTTCTTGTGTTTCCTCTTTTAAATGTCTGGTTTAGCCTTAAGTAGTATTTACTGAGTGCCACATGATCCAGTGGTTGGAGTATGTAGGTTTTGCCCTTATCTTCATTCTTTGCATCTGTTTGAACTCATGACAATACAAAACAAGGTGTTCCTGGGATAGGGAATGTTTTGTCCAAAAGGAGTCAACACGGAGAAAACTCTTCCTACAGTTAAGACAGGGTTTGGTTTTGTTTTTAAATGAGGAGAGAAACTGAGAAGTGGAAAACACA... |
Task1_train_39103 | Located on Chromosome 9, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TAAGCCCATGGAGGTAGTCAGGAGCTGAGTGCCCTTGACCTCCATTTAGAAAGGCAGCCCAGTCTGCAAAAGACAGCAGCAGGGACATCTCATCCCAGGCCTCCTGGTTATGCTGCTGACTTTGTCTGTCTGCTACTGACTTTTAGTTTTTTTGTGTGCCTCAGATAACACTTTGAAAAACAGGAATCTTAATGTCTGCTGTCTATATTCCAAGAGACTGTAGATGACCAATGAAATTATCTACTGGACAATGCTTTCATGTCTTTTTTTTTTTTTTTTTTAATTGAGACGGAGTTTTTGCTCTGTTGCCCAGGCTAGAA... | TAAGCCCATGGAGGTAGTCAGGAGCTGAGTGCCCTTGACCTCCATTTAGAAAGGCAGCCCAGTCTGCAAAAGACAGCAGCAGGGACATCTCATCCCAGGCCTCCTGGTTATGCTGCTGACTTTGTCTGTCTGCTACTGACTTTTAGTTTTTTTGTGTGCCTCAGATAACACTTTGAAAAACAGGAATCTTAATGTCTGCTGTCTATATTCCAAGAGACTGTAGATGACCAATGAAATTATCTACTGGACAATGCTTTCATGTCTTTTTTTTTTTTTTTTTTAATTGAGACGGAGTTTTTGCTCTGTTGCCCAGGCTAGAA... |
Task1_train_39104 | This sequence variant lies on Chromosome 9. Is it clinically significant, and what condition might it cause if any? | Benign | AAAGATGGAAAAAGATGGAAATAGTAGACATTTTAGACTACAAAAGTGGGGAAAGAGGGGAGTGAGGGTTGAAAAATTACCTATTGAGTACGGTGTGCACTATTTGGGTGATGTGTACACTAGAAGCTCAAAGCTCATCATTACACAATATATCCTTGTAACAAGCCTGCACATGTACTCCCTGAATCTAACATACAGTTTTAAAAAATAATACAATCATTATCTCATTACATTGTTTTTAAGCCTGTGAGTTAAATATTTGCATCTCCATTTTTACTCAGGGAGAAACTGAAGTTAAGAGAGGTTTATTAACTTGCTTA... | AAAGATGGAAAAAGATGGAAATAGTAGACATTTTAGACTACAAAAGTGGGGAAAGAGGGGAGTGAGGGTTGAAAAATTACCTATTGAGTACGGTGTGCACTATTTGGGTGATGTGTACACTAGAAGCTCAAAGCTCATCATTACACAATATATCCTTGTAACAAGCCTGCACATGTACTCCCTGAATCTAACATACAGTTTTAAAAAATAATACAATCATTATCTCATTACATTGTTTTTAAGCCTGTGAGTTAAATATTTGCATCTCCATTTTTACTCAGGGAGAAACTGAAGTTAAGAGAGGTTTATTAACTTGCTTA... |
Task1_train_39105 | A variant affecting Chromosome 9 has been observed. Determine if it's benign or associated with disease. | Benign | GCACTATTTGGGTGATGTGTACACTAGAAGCTCAAAGCTCATCATTACACAATATATCCTTGTAACAAGCCTGCACATGTACTCCCTGAATCTAACATACAGTTTTAAAAAATAATACAATCATTATCTCATTACATTGTTTTTAAGCCTGTGAGTTAAATATTTGCATCTCCATTTTTACTCAGGGAGAAACTGAAGTTAAGAGAGGTTTATTAACTTGCTTACCCAAGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAGGTTGGGTGGATCACCTAAGGTCAGGAGTTCGAGACCAGCCTG... | GCACTATTTGGGTGATGTGTACACTAGAAGCTCAAAGCTCATCATTACACAATATATCCTTGTAACAAGCCTGCACATGTACTCCCTGAATCTAACATACAGTTTTAAAAAATAATACAATCATTATCTCATTACATTGTTTTTAAGCCTGTGAGTTAAATATTTGCATCTCCATTTTTACTCAGGGAGAAACTGAAGTTAAGAGAGGTTTATTAACTTGCTTACCCAAGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAGGTTGGGTGGATCACCTAAGGTCAGGAGTTCGAGACCAGCCTG... |
Task1_train_39106 | Located on Chromosome 9, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | AAAAGAACATAAATATTGGATAACAGCAATTGACATGCGTGTTTTAATGGAAGATTGTTTTAATGGAAGATTTAAGTGGTTATCATTTATAAGTTTCCAGGATGGAATAGATTGTTGCATCCTAGCTCCTGTCAGGAGTAGAGCTTCACTGGTTTCACAGGTAGGGTATGAGGTGCTGTGTAAAGCTAGAAGCTTCTTTTGGAAGTAATTTTCAGACAGAGAATACTAATGGAGAAATTTCAGACTGAGGGAAAGGGCCTGTGAGAGAGGCCTCAGAATTAGAGCTCCAAAGGCAGATTCGAGGATTTCAGAACTCAGTG... | AAAAGAACATAAATATTGGATAACAGCAATTGACATGCGTGTTTTAATGGAAGATTGTTTTAATGGAAGATTTAAGTGGTTATCATTTATAAGTTTCCAGGATGGAATAGATTGTTGCATCCTAGCTCCTGTCAGGAGTAGAGCTTCACTGGTTTCACAGGTAGGGTATGAGGTGCTGTGTAAAGCTAGAAGCTTCTTTTGGAAGTAATTTTCAGACAGAGAATACTAATGGAGAAATTTCAGACTGAGGGAAAGGGCCTGTGAGAGAGGCCTCAGAATTAGAGCTCCAAAGGCAGATTCGAGGATTTCAGAACTCAGTG... |
Task1_train_39107 | A variant on Chromosome 9 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GGGCAGTACAGAGAAAAGCGGCCTCCCCGAGGGGACAAGGGCCTCTGTGCCCATGAGGGGTCGGACATTGCAGCGGACTTGCCTACGCTCTCATCTAGCATTTGATTCCCCACCAGGAGATGGGCTTGGTGCACGCTCTCAGAAGCGCATCCACCGAAGGCTCTGGAACTGCCCCGCTTCGCATAGAGCTATTGTGCTGCCCTGCAGTGTATCCACTTGTTTTGTTTGTTTGTTTGTTTTTTGGTTTTTGCTTGTTTGCTGATGGGCAGTGGGGAGGTGCGAGGGTGGAGGGCCTTCTTTGTGCATATATAGCGATAGTC... | GGGCAGTACAGAGAAAAGCGGCCTCCCCGAGGGGACAAGGGCCTCTGTGCCCATGAGGGGTCGGACATTGCAGCGGACTTGCCTACGCTCTCATCTAGCATTTGATTCCCCACCAGGAGATGGGCTTGGTGCACGCTCTCAGAAGCGCATCCACCGAAGGCTCTGGAACTGCCCCGCTTCGCATAGAGCTATTGTGCTGCCCTGCAGTGTATCCACTTGTTTTGTTTGTTTGTTTGTTTTTTGGTTTTTGCTTGTTTGCTGATGGGCAGTGGGGAGGTGCGAGGGTGGAGGGCCTTCTTTGTGCATATATAGCGATAGTC... |
Task1_train_39108 | This variant is found on Chromosome 9. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CCCTTAAGGCTTTTAAAATGACAAGTGTAGGAGAAGATTGTTTCTAGAGGGTGCTTTGATGAAATTTCACCGGCTGGCTATCTGTATATAATCAGGTGTGCCCACAGAGAAGGCAACAATGAAGCTATTCAGGCAGGGCAGCAGAAAACACAGGCAAAGCAATTGTTTACAACTCAACAACTGGGTCATTAGGAATTTTCATCTTTCGATCAGCTACCCTGGCTTTGAGTAGCCACAGCCAGCGCGTGTTTCAAAAAAGGACAAAACTCTATTTGCAAATAGCTTGCTACTAAAAAATATGTTTCTTTATTATAAAGTCC... | CCCTTAAGGCTTTTAAAATGACAAGTGTAGGAGAAGATTGTTTCTAGAGGGTGCTTTGATGAAATTTCACCGGCTGGCTATCTGTATATAATCAGGTGTGCCCACAGAGAAGGCAACAATGAAGCTATTCAGGCAGGGCAGCAGAAAACACAGGCAAAGCAATTGTTTACAACTCAACAACTGGGTCATTAGGAATTTTCATCTTTCGATCAGCTACCCTGGCTTTGAGTAGCCACAGCCAGCGCGTGTTTCAAAAAAGGACAAAACTCTATTTGCAAATAGCTTGCTACTAAAAAATATGTTTCTTTATTATAAAGTCC... |
Task1_train_39109 | This variant is found on Chromosome 9. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TAATATATTGACTATTTTTAACCGTTTCTCTTTAAATTTTTAAAAATTTAAATAAGGGACAATTAATGTTTGCTTTAATCACTGCCACTTCATGAAATTCAGGTTGAAAGTAAACAAAAATTTTTAAGTAGACATTTGGATTCTGTTTTTTTCTTGTGTAGCTTCTGAATTTTGTTGGTTCTGGACAGGTTTGTGTGTGTCCTATAAAAATTTTTAAGTAGACATTTGGATTCTGTTTTTTTCTTGTGTAGCTTCTGAATTTTGTTGGTTCTGGACAGGTTTTGAAGTTTGTGTGTGTCCTATCATGTGTTGTATACTTC... | TAATATATTGACTATTTTTAACCGTTTCTCTTTAAATTTTTAAAAATTTAAATAAGGGACAATTAATGTTTGCTTTAATCACTGCCACTTCATGAAATTCAGGTTGAAAGTAAACAAAAATTTTTAAGTAGACATTTGGATTCTGTTTTTTTCTTGTGTAGCTTCTGAATTTTGTTGGTTCTGGACAGGTTTGTGTGTGTCCTATAAAAATTTTTAAGTAGACATTTGGATTCTGTTTTTTTCTTGTGTAGCTTCTGAATTTTGTTGGTTCTGGACAGGTTTTGAAGTTTGTGTGTGTCCTATCATGTGTTGTATACTTC... |
Task1_train_39110 | A mutation on Chromosome 9 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TCTGTTTTTTTCTTGTGTAGCTTCTGAATTTTGTTGGTTCTGGACAGGTTTTGAAGTTTGTGTGTGTCCTATCATGTGTTGTATACTTCTGACCATAGAGTGGTTTCTTATGAATTAAAAATGAATTTGGTTACAAACTGGATAAACAGATTTATAATAATAGGGCCACATTGATAAACTGAGATTATGCAAAGCAACTTGTGAAGTCTGAGGACTAAATGGAATAGTAAATTCAACTAAATAACTTCCTGGCAAAAACTTATCATAGAAATGTAAACATTAATTTTCAAATTTTATTTTATTTGCAAATGAGTATAATG... | TCTGTTTTTTTCTTGTGTAGCTTCTGAATTTTGTTGGTTCTGGACAGGTTTTGAAGTTTGTGTGTGTCCTATCATGTGTTGTATACTTCTGACCATAGAGTGGTTTCTTATGAATTAAAAATGAATTTGGTTACAAACTGGATAAACAGATTTATAATAATAGGGCCACATTGATAAACTGAGATTATGCAAAGCAACTTGTGAAGTCTGAGGACTAAATGGAATAGTAAATTCAACTAAATAACTTCCTGGCAAAAACTTATCATAGAAATGTAAACATTAATTTTCAAATTTTATTTTATTTGCAAATGAGTATAATG... |
Task1_train_39111 | A mutation on Chromosome 9 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GGAAGCTGTTTATAGGGCTCACCTAATGGTCCAGTTTATTAGCCTGCTTGTCCATAGTCTGTCAGGTGGGTTTTTTGGAGAGACATATCCACTGACGCGTGCCTGACAGCATTAGAGTGCGCCACACTCCAAGGCACATTTAGATTACGCTCTCAAGGATACATTTTCTTACCCCTATTGCCTGTCTTCTGCCCATTCATTTCCTATACTCCTGTGTCAGGGAGAGCCCACACCTGTATAAATGGACATATTTCACTTTGTCTTTCCACACTGTTTAGAAATGCCCATTATGACTGGCTTCTTTCATCTATTTCTTTCGA... | GGAAGCTGTTTATAGGGCTCACCTAATGGTCCAGTTTATTAGCCTGCTTGTCCATAGTCTGTCAGGTGGGTTTTTTGGAGAGACATATCCACTGACGCGTGCCTGACAGCATTAGAGTGCGCCACACTCCAAGGCACATTTAGATTACGCTCTCAAGGATACATTTTCTTACCCCTATTGCCTGTCTTCTGCCCATTCATTTCCTATACTCCTGTGTCAGGGAGAGCCCACACCTGTATAAATGGACATATTTCACTTTGTCTTTCCACACTGTTTAGAAATGCCCATTATGACTGGCTTCTTTCATCTATTTCTTTCGA... |
Task1_train_39112 | This mutation on Chromosome 9 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | CATTGACCTTTAAGTTGCTATTCAAATCTGATTACAAGGTTTCCATTTTGATTATGTAGATATCAATGTCAATGTTGTTGTCTCATTTTGACTTAATAACCTTTGGTAACTAAAACCTTAAAAAAAAAATCAGAGGCTTTCAGTCTTTACTGTATCTTAACTCCAACCTGACTATTCTTTCCAAGTATATTTATACCTATGTTCTCAGACTACAAATCATTCTTTTCCTGATTACTCAAGGTAGAGTCTTACCACTTTCACAGTCCCCAAAGGTAGTAAGGTCATATAGAACTGCAAGACACGTACCCTCAGCATTGAGA... | CATTGACCTTTAAGTTGCTATTCAAATCTGATTACAAGGTTTCCATTTTGATTATGTAGATATCAATGTCAATGTTGTTGTCTCATTTTGACTTAATAACCTTTGGTAACTAAAACCTTAAAAAAAAAATCAGAGGCTTTCAGTCTTTACTGTATCTTAACTCCAACCTGACTATTCTTTCCAAGTATATTTATACCTATGTTCTCAGACTACAAATCATTCTTTTCCTGATTACTCAAGGTAGAGTCTTACCACTTTCACAGTCCCCAAAGGTAGTAAGGTCATATAGAACTGCAAGACACGTACCCTCAGCATTGAGA... |
Task1_train_39113 | This genomic variant is located on Chromosome 9. Can you determine its pathogenicity and name any linked disease? | Benign | CACTCAATAAATGTTGGTCTTTGCCTCTTCTCAGTGGAGGCCAGCTTCAGCATGGGGGACCCTGGGATTGCATACATGATATATATATAATAATATTATTGCTTACACACCCTGTGCCAGGCACTCCTTCAATTCCTATAACAACTCTGTGAGGTAGATACCACACATTTCAAAAGTAGAAACTGAGGCCAAGAGAATTTAGGTGATCTGCCCAACTTATTCAGCTGGGAAGTGGATTCAGACCCACAAGTCTACTGTAGTCCGTTTCCTTCAGCTTATCTACACCACATTACCTCTCTTGGATGCCTGCTTGTATTTTG... | CACTCAATAAATGTTGGTCTTTGCCTCTTCTCAGTGGAGGCCAGCTTCAGCATGGGGGACCCTGGGATTGCATACATGATATATATATAATAATATTATTGCTTACACACCCTGTGCCAGGCACTCCTTCAATTCCTATAACAACTCTGTGAGGTAGATACCACACATTTCAAAAGTAGAAACTGAGGCCAAGAGAATTTAGGTGATCTGCCCAACTTATTCAGCTGGGAAGTGGATTCAGACCCACAAGTCTACTGTAGTCCGTTTCCTTCAGCTTATCTACACCACATTACCTCTCTTGGATGCCTGCTTGTATTTTG... |
Task1_train_39114 | Here is a genetic alteration on Chromosome 9. Based on the data, is it a benign variant or a cause of disease? | Benign | TTTTTTTGTCAAATCTTCCTAACAACTGAAGAGAGAAGATAGATGAAATGCCCCCCACTTAACAAATGTGAACTAAGACTCCATGATTTGCCCAGAGTCACACAGTTCAGGGTAGACTAGTGTTTGCATTCAAATTGGTCTAATTTCAAAACACTTTTTAAAGATTTCTTTAGAGAAAAAAGAAGAAATCACCCATTATCCTACCATCCTGATATAAAACCGTCAATATTTTGGAGAACTTCCTTCCAATTTTTCTTCTACACATAGGTCAATTTTCAAATTTTTAAAAATGTGTTTCACAGTTGTAATCAAAATGTGTT... | TTTTTTTGTCAAATCTTCCTAACAACTGAAGAGAGAAGATAGATGAAATGCCCCCCACTTAACAAATGTGAACTAAGACTCCATGATTTGCCCAGAGTCACACAGTTCAGGGTAGACTAGTGTTTGCATTCAAATTGGTCTAATTTCAAAACACTTTTTAAAGATTTCTTTAGAGAAAAAAGAAGAAATCACCCATTATCCTACCATCCTGATATAAAACCGTCAATATTTTGGAGAACTTCCTTCCAATTTTTCTTCTACACATAGGTCAATTTTCAAATTTTTAAAAATGTGTTTCACAGTTGTAATCAAAATGTGTT... |
Task1_train_39115 | A change on Chromosome 9 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | ATGTCTTTGCAAAGCCTGGCAACAGTAGAAAAATGGGGAAATCCTATTGCACAAAAATTAATTTTGCAATGCAAAAAATATTTTTCTGGATAATTCGAGCCTTTATGTTTATTTCAGTAAAGCCAAATCCAGTGAACTATTTTCAGCCAGGATTAGTCAGAACTAAAAGGTTGGACTGTTTTCCTTCAGAGGCTGAATGTCTTTCCTGCCTGCAATAGGCCGGTGTGTTCCAGAGTAAATTGAATTGCCTTCAATTGCTTGTTTCTTTGTGGCATTTTTAATGCAGAACCCTAGTGACAGAGTAAGGTTTTGCTGTCTGG... | ATGTCTTTGCAAAGCCTGGCAACAGTAGAAAAATGGGGAAATCCTATTGCACAAAAATTAATTTTGCAATGCAAAAAATATTTTTCTGGATAATTCGAGCCTTTATGTTTATTTCAGTAAAGCCAAATCCAGTGAACTATTTTCAGCCAGGATTAGTCAGAACTAAAAGGTTGGACTGTTTTCCTTCAGAGGCTGAATGTCTTTCCTGCCTGCAATAGGCCGGTGTGTTCCAGAGTAAATTGAATTGCCTTCAATTGCTTGTTTCTTTGTGGCATTTTTAATGCAGAACCCTAGTGACAGAGTAAGGTTTTGCTGTCTGG... |
Task1_train_39116 | This alteration on Chromosome 9 may affect genome function. Does it lead to a disease or is it benign? | Benign | AGACCAGCAGCATTCATATCACCTGGAAGCTTGTTAGAAAAGGAGAATCCTAAGCTCCACCCCAGCCCTACTGAATCAGAATCTGCAGTTTAACAAGAGCCCCAGGTGATTCAACTGCACATTCAGGTTTGAGAAGCACTGCTGTGTTCTACCTTAGGCCTGGATGAATGAGCTGACAGGTGACCTAAGCAAAGGGCTGGCTTGAAAGCTACAGGGATTCCAAGGATCTGAGCCCAGAGGTCTGAATGTCTTCTCTAAATGTAGGTATGCCAAAAACTTGGTGTGTGACCTTTACACACATTGTAATCTCTCTGGAACCT... | AGACCAGCAGCATTCATATCACCTGGAAGCTTGTTAGAAAAGGAGAATCCTAAGCTCCACCCCAGCCCTACTGAATCAGAATCTGCAGTTTAACAAGAGCCCCAGGTGATTCAACTGCACATTCAGGTTTGAGAAGCACTGCTGTGTTCTACCTTAGGCCTGGATGAATGAGCTGACAGGTGACCTAAGCAAAGGGCTGGCTTGAAAGCTACAGGGATTCCAAGGATCTGAGCCCAGAGGTCTGAATGTCTTCTCTAAATGTAGGTATGCCAAAAACTTGGTGTGTGACCTTTACACACATTGTAATCTCTCTGGAACCT... |
Task1_train_39117 | A mutation on Chromosome 9 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GGAAAAATTGGGTAACATGATCTGCAAACAGGTCAAAATACTTGAACTAGGGACTCTTCCAAATAGCTACAATATAGAGTTGCTGATTTGTTTTTTACTTTCTGTTTTTTAACATTTTAATAAGGCAGGTTATAATGTTACTTTTCATTCTACTTTAATATATTGACTTGAATTTACAGTCTTTATAACATCAGGTTTTCTAAATTTTAATGCTTCTACTTAAGGAAACATCACATATCATCAGAAAATCTGACTAAATAAAAAAATTAAATATGTAAAATCACTGATAAAAGACTTTGGCACATAGGAAAAGCTGTATA... | GGAAAAATTGGGTAACATGATCTGCAAACAGGTCAAAATACTTGAACTAGGGACTCTTCCAAATAGCTACAATATAGAGTTGCTGATTTGTTTTTTACTTTCTGTTTTTTAACATTTTAATAAGGCAGGTTATAATGTTACTTTTCATTCTACTTTAATATATTGACTTGAATTTACAGTCTTTATAACATCAGGTTTTCTAAATTTTAATGCTTCTACTTAAGGAAACATCACATATCATCAGAAAATCTGACTAAATAAAAAAATTAAATATGTAAAATCACTGATAAAAGACTTTGGCACATAGGAAAAGCTGTATA... |
Task1_train_39118 | Consider this mutation on Chromosome 9. Is this a benign change or a disease-causing variant? | Benign | AAAACCCCATCAAAAAGTGGGTGAAGGACATGAACAGACACTTCTCAAAAGAAGACATTTACACAGCCAACAGACACATGAAAAAATACTCATCATCACTGGTCATCAGAGAAATACAAATCAAAACCACAATGAGATACCATCTCACACAGTTAGAATGGCGATCATTAAAAAGTCAGGAAACAACAGGTGCTGGAGAGAATGTGGAGAAACAGGAACACCTTTACACTGTTGGTGGGACAGTAAACTAGTTCAACCCATGTGGAAGACAGTGTGGTGATTCCTCAAGGATCTAGAACTAGAAATACCATTTGACCCAG... | AAAACCCCATCAAAAAGTGGGTGAAGGACATGAACAGACACTTCTCAAAAGAAGACATTTACACAGCCAACAGACACATGAAAAAATACTCATCATCACTGGTCATCAGAGAAATACAAATCAAAACCACAATGAGATACCATCTCACACAGTTAGAATGGCGATCATTAAAAAGTCAGGAAACAACAGGTGCTGGAGAGAATGTGGAGAAACAGGAACACCTTTACACTGTTGGTGGGACAGTAAACTAGTTCAACCCATGTGGAAGACAGTGTGGTGATTCCTCAAGGATCTAGAACTAGAAATACCATTTGACCCAG... |
Task1_train_39119 | Mutation context: Chromosome 9. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | AGTATTTCCACTTCAGCAAACTGTCTTTTACATAGTTTCCATAGTAGCAGGTTTTGTGGGTATAACAATTTTCAAATATTTTCAGATACATTTTTATTTTCTACAAGTCTTGTTTCATTGCAGCTTCCTGCTCATTATTAATGACATTTATTCTTCCAGGGGAGTGTGAATAATACTTAAAACAAAAGGATCATTAACAAGCTGAGTTTTAAGGTTGAACATTTTTATTAAGAAAACTGTCTTTAGAGCACTTTGTTGAGAAAAGGCATTCCAACCTCTCTTTAAATAACAGCCTCAAGCTTGGAGGTCTAAAAATAAAA... | AGTATTTCCACTTCAGCAAACTGTCTTTTACATAGTTTCCATAGTAGCAGGTTTTGTGGGTATAACAATTTTCAAATATTTTCAGATACATTTTTATTTTCTACAAGTCTTGTTTCATTGCAGCTTCCTGCTCATTATTAATGACATTTATTCTTCCAGGGGAGTGTGAATAATACTTAAAACAAAAGGATCATTAACAAGCTGAGTTTTAAGGTTGAACATTTTTATTAAGAAAACTGTCTTTAGAGCACTTTGTTGAGAAAAGGCATTCCAACCTCTCTTTAAATAACAGCCTCAAGCTTGGAGGTCTAAAAATAAAA... |
Task1_train_39120 | This variant is located on Chromosome 9. Evaluate its biological effect and specify any disease association. | Benign | CTCTGCCATTCTCCAGGATGTTGTCCCTATAAAATTGTCAAAGCTCAGTCAGTGCCAAACCCATGTTTCAACCTTCAGAAAGTAAACGAGTGGTGGAAAACACATTCAATGTTTTAAGGCCAAGACCTTGAAAACTCACTCTCTTAGCCTGAACTTAGATTACATGGCTGGGCCCACTTAACTATAGGGGAGGCTTGGAAACATAGTCTCTGAGAAGCCATGTGTCCAGCTAATTCCCTAATACTAAAGTTGAAAGAAAGAATGGATTAACCAGCAGTATACCACAAGGTAACAAATGACTAGGAGGATCAGGCTAGGTG... | CTCTGCCATTCTCCAGGATGTTGTCCCTATAAAATTGTCAAAGCTCAGTCAGTGCCAAACCCATGTTTCAACCTTCAGAAAGTAAACGAGTGGTGGAAAACACATTCAATGTTTTAAGGCCAAGACCTTGAAAACTCACTCTCTTAGCCTGAACTTAGATTACATGGCTGGGCCCACTTAACTATAGGGGAGGCTTGGAAACATAGTCTCTGAGAAGCCATGTGTCCAGCTAATTCCCTAATACTAAAGTTGAAAGAAAGAATGGATTAACCAGCAGTATACCACAAGGTAACAAATGACTAGGAGGATCAGGCTAGGTG... |
Task1_train_39121 | A mutation is present on Chromosome 9. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GAGCCACCGCGCCTGGCCTTTGCTCTTCCCTTTTAATCCTAACTAGAATGGGTATGTCAGACGCCTGGAAATGCAACAGCCTTCTTGAGACCATGCGGATGAAAATTTTATGCAAAGGAGGGCAGAGCGGGAAAACTGAAGGAGCACCAGTGCTTGGCTTATTACCTCTGGACTTAAATGAGAAAAGATAAATTGCTATTTGATTGACCTTCCATAGCTGGAGTACAGTTACATGCACTCTAACTCAGTTCCAACAAAAAGGGTCAAAGTGGTTTTCACTGTTGACCAAGACAACTGTTTCTTCAGCCAGTCGAAGGCAA... | GAGCCACCGCGCCTGGCCTTTGCTCTTCCCTTTTAATCCTAACTAGAATGGGTATGTCAGACGCCTGGAAATGCAACAGCCTTCTTGAGACCATGCGGATGAAAATTTTATGCAAAGGAGGGCAGAGCGGGAAAACTGAAGGAGCACCAGTGCTTGGCTTATTACCTCTGGACTTAAATGAGAAAAGATAAATTGCTATTTGATTGACCTTCCATAGCTGGAGTACAGTTACATGCACTCTAACTCAGTTCCAACAAAAAGGGTCAAAGTGGTTTTCACTGTTGACCAAGACAACTGTTTCTTCAGCCAGTCGAAGGCAA... |
Task1_train_39122 | An alteration has been detected on Chromosome 9. Is it pathogenic, and if so, what disease is involved? | Benign | GCCCAGACTTATGATGCTTATTTTCTGTCTTTTTTTTTTCCCTGATATTTATTTTCTGCTTATTTAGAGTGGTAGTGAGTGGAAGAACCTTAGGAACATGGAGTCAAACTTCGGCATCTTATAAGAGGTAGACCTGAGGTGCAGAACTAACTCAGGTGTTGATATTTCCCCCTGTAGTTTACCGCAATGATCGTCAAAGTGTTTGTTAGTAGGTCAGGACCAACATTTTAAAATGAGGTGGTAAAATAGAATAAAAAGTATTATAGTGCTTCCTCTGTGGTAAGGGCAAATATTCACTCATGACATGTGTGAGTATGTGT... | GCCCAGACTTATGATGCTTATTTTCTGTCTTTTTTTTTTCCCTGATATTTATTTTCTGCTTATTTAGAGTGGTAGTGAGTGGAAGAACCTTAGGAACATGGAGTCAAACTTCGGCATCTTATAAGAGGTAGACCTGAGGTGCAGAACTAACTCAGGTGTTGATATTTCCCCCTGTAGTTTACCGCAATGATCGTCAAAGTGTTTGTTAGTAGGTCAGGACCAACATTTTAAAATGAGGTGGTAAAATAGAATAAAAAGTATTATAGTGCTTCCTCTGTGGTAAGGGCAAATATTCACTCATGACATGTGTGAGTATGTGT... |
Task1_train_39123 | This mutation on Chromosome 9 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GTTGATTAGGTTTCACATATAAGTAGTAGGTGGTTGATGATCAGATGTCTTAAATGGATGTTCACTATGACAAGTATCTGACTAGTCCACATAGCTTAATCAGTAATCTACCAAAGTCATGGGTAACTCAACCAATAGTCCCAGGGAATATTGTAAAAGTCAGGAGCCTCACTGCTATGTGTAGCAGAATTGTGAGACAAGCAGTCAGCAGTGCCTATTTGGTTTAATAAAAAAGAAGATTCTAAAATGAGTTTTTTTTTTTTCGTGCAACTCAATTTACAATATACGTTTTTGGAAGGCTTCTTTTGAATTCACATGAG... | GTTGATTAGGTTTCACATATAAGTAGTAGGTGGTTGATGATCAGATGTCTTAAATGGATGTTCACTATGACAAGTATCTGACTAGTCCACATAGCTTAATCAGTAATCTACCAAAGTCATGGGTAACTCAACCAATAGTCCCAGGGAATATTGTAAAAGTCAGGAGCCTCACTGCTATGTGTAGCAGAATTGTGAGACAAGCAGTCAGCAGTGCCTATTTGGTTTAATAAAAAAGAAGATTCTAAAATGAGTTTTTTTTTTTTCGTGCAACTCAATTTACAATATACGTTTTTGGAAGGCTTCTTTTGAATTCACATGAG... |
Task1_train_39124 | Mutation context: Chromosome 9. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | AAAGAGAAGCCTGTTAAAGGAAACTGAGGGTCAGCTAGAGGTGCAGGAGGACAATGAGGAGTCTAAGGGTCATGGAAACCACAGGGAGAAAATCTTTCAGGAAGGATCAACAGTGTTGTATGGTGCTAAGAGGTCAGGTGAACCAAGGACTTGGAATTGTCTATTAGATACTGTGACTTGGAGGGGAGGCTAGGAAGAGTGAATATCTTCTTGTGATGGTGGAGAATCTTAAAATCCATTTAAAATCTTGAGCCTACACATTGTATTTTAGAAGACTTTTTCCTCTTGTTAGATTAGTGCTCTAGAACATGTGTACCTGT... | AAAGAGAAGCCTGTTAAAGGAAACTGAGGGTCAGCTAGAGGTGCAGGAGGACAATGAGGAGTCTAAGGGTCATGGAAACCACAGGGAGAAAATCTTTCAGGAAGGATCAACAGTGTTGTATGGTGCTAAGAGGTCAGGTGAACCAAGGACTTGGAATTGTCTATTAGATACTGTGACTTGGAGGGGAGGCTAGGAAGAGTGAATATCTTCTTGTGATGGTGGAGAATCTTAAAATCCATTTAAAATCTTGAGCCTACACATTGTATTTTAGAAGACTTTTTCCTCTTGTTAGATTAGTGCTCTAGAACATGTGTACCTGT... |
Task1_train_39125 | The following genetic variant occurs on Chromosome 9. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | AAGGAAACTGAGGGTCAGCTAGAGGTGCAGGAGGACAATGAGGAGTCTAAGGGTCATGGAAACCACAGGGAGAAAATCTTTCAGGAAGGATCAACAGTGTTGTATGGTGCTAAGAGGTCAGGTGAACCAAGGACTTGGAATTGTCTATTAGATACTGTGACTTGGAGGGGAGGCTAGGAAGAGTGAATATCTTCTTGTGATGGTGGAGAATCTTAAAATCCATTTAAAATCTTGAGCCTACACATTGTATTTTAGAAGACTTTTTCCTCTTGTTAGATTAGTGCTCTAGAACATGTGTACCTGTTAATGATCCTAATCAG... | AAGGAAACTGAGGGTCAGCTAGAGGTGCAGGAGGACAATGAGGAGTCTAAGGGTCATGGAAACCACAGGGAGAAAATCTTTCAGGAAGGATCAACAGTGTTGTATGGTGCTAAGAGGTCAGGTGAACCAAGGACTTGGAATTGTCTATTAGATACTGTGACTTGGAGGGGAGGCTAGGAAGAGTGAATATCTTCTTGTGATGGTGGAGAATCTTAAAATCCATTTAAAATCTTGAGCCTACACATTGTATTTTAGAAGACTTTTTCCTCTTGTTAGATTAGTGCTCTAGAACATGTGTACCTGTTAATGATCCTAATCAG... |
Task1_train_39126 | Chromosome 9 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CCTTGGTCTGCCAAAGTCCTGGGATTACGGGTATGAGCCACTGTGCCCAGCATTGCTGAGCAATTTTTATATAATCTATTCTTGAATCTCAATCAGAATGAAAACTTTTGTTTAGAAAGTCACGTATAAATGATGTTTGACCACGTTATTTTTCAGCTTATAAGTAAGTTTTGATCAAGTCCACGTGACTGTCTTTATATTATAAAGGAATGCATATATTTTTGCAATATTCCAGGCATCTTATTAAATTCAGATTTAGCAATTTACCTATATACTATTTGCAGTTTTCATTACTTGCTATTAACCCTAAAGGACTAGAT... | CCTTGGTCTGCCAAAGTCCTGGGATTACGGGTATGAGCCACTGTGCCCAGCATTGCTGAGCAATTTTTATATAATCTATTCTTGAATCTCAATCAGAATGAAAACTTTTGTTTAGAAAGTCACGTATAAATGATGTTTGACCACGTTATTTTTCAGCTTATAAGTAAGTTTTGATCAAGTCCACGTGACTGTCTTTATATTATAAAGGAATGCATATATTTTTGCAATATTCCAGGCATCTTATTAAATTCAGATTTAGCAATTTACCTATATACTATTTGCAGTTTTCATTACTTGCTATTAACCCTAAAGGACTAGAT... |
Task1_train_39127 | This variant is found on Chromosome 9. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GATCATCTGAGGTCAGGAGTTCGAGACCAGCCTCGCCAACGTGGTGCAACCCCGTCTCTACTAAAAAAATGTATAAAAATTAGCCAGGCATGGTTGGCGGCATGCTTATAATTACAGCTACTTGAGAGGCTGAGGCAGAAGAATCACTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCGCCGTTGCACTCCAGCCTAGGCAACAAGAGCGAAACTCCGTCTCAAGAGAAAACCAAAAACCAAAAAAAAATTAGTGTAAATTTTTTTCAAACTCTAGATTTTTTTTTTATTAACATGGCACAGCTGTGTGGT... | GATCATCTGAGGTCAGGAGTTCGAGACCAGCCTCGCCAACGTGGTGCAACCCCGTCTCTACTAAAAAAATGTATAAAAATTAGCCAGGCATGGTTGGCGGCATGCTTATAATTACAGCTACTTGAGAGGCTGAGGCAGAAGAATCACTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCGCCGTTGCACTCCAGCCTAGGCAACAAGAGCGAAACTCCGTCTCAAGAGAAAACCAAAAACCAAAAAAAAATTAGTGTAAATTTTTTTCAAACTCTAGATTTTTTTTTTATTAACATGGCACAGCTGTGTGGT... |
Task1_train_39128 | This mutation on Chromosome 9 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GGTATGTGGGGGAAGCCGTGGAGGTGGCCTGTTACCCTGAGTAACTGTCCCATGAACTGGCTGGAAACATGAACAGCTTTACGCTTCGGTACATTTTTTGTTTTCAGGCTTCCTTGTGGCTGTTTTCTTGTTTTTCTCTTCTTTACTATGGACCGTGTGTTTTCAAGTCCTAAAGTGTCTTTCACCTCTGCCTCTGCCAGCAGCCAGGGGAAGCAGTCTCAGCACAGTGAAATGTGCTGTGTGTTGATGTCATCAGAAGTCATCCACCTCAGTGAAAACAGCTGCCAGTGCATTTTAGGAGGCAAGATAGTAGGGAATTG... | GGTATGTGGGGGAAGCCGTGGAGGTGGCCTGTTACCCTGAGTAACTGTCCCATGAACTGGCTGGAAACATGAACAGCTTTACGCTTCGGTACATTTTTTGTTTTCAGGCTTCCTTGTGGCTGTTTTCTTGTTTTTCTCTTCTTTACTATGGACCGTGTGTTTTCAAGTCCTAAAGTGTCTTTCACCTCTGCCTCTGCCAGCAGCCAGGGGAAGCAGTCTCAGCACAGTGAAATGTGCTGTGTGTTGATGTCATCAGAAGTCATCCACCTCAGTGAAAACAGCTGCCAGTGCATTTTAGGAGGCAAGATAGTAGGGAATTG... |
Task1_train_39129 | Here is a mutation located on Chromosome 9. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AAACAAAAACAAAAACAAAAACAAACAAACAAACAAACAAACAAAAAGCTTTGTAGTAAGAACCATGTTCTATATGTTTTTCTGTTTCTCCTAAATAACACTGTCCCTGCAATACAGATTAAAAACTCACTGTTAAATTAATGAAAATCTGTGTTACAATGAATACTAGGACACGTTGTAAAAGAACTCGGATAGCAAAACTGGGAGTCTGAGCAGAAGAATCTTTCACTACATTAAGCAGTATCTTCTTTTACGACCTCTATAATTTTGAGATATAATGTTCCTATTTACCTATAATTCTTTCCTTCAGCCCTAAGCCT... | AAACAAAAACAAAAACAAAAACAAACAAACAAACAAACAAACAAAAAGCTTTGTAGTAAGAACCATGTTCTATATGTTTTTCTGTTTCTCCTAAATAACACTGTCCCTGCAATACAGATTAAAAACTCACTGTTAAATTAATGAAAATCTGTGTTACAATGAATACTAGGACACGTTGTAAAAGAACTCGGATAGCAAAACTGGGAGTCTGAGCAGAAGAATCTTTCACTACATTAAGCAGTATCTTCTTTTACGACCTCTATAATTTTGAGATATAATGTTCCTATTTACCTATAATTCTTTCCTTCAGCCCTAAGCCT... |
Task1_train_39130 | This mutation is located on Chromosome 9. Is it associated with a disease or is it a benign polymorphism? | Benign | CCCTTGATTCTGTAAGTGGTAGTTCTAACTTTGAAATGGGTCATCTAACTTATAACTATTTTCTTCATTTCTTTTTAAAAGGGAGAAATAGCATGCAAATTTCTGGCATGTTGATAGAAAGTTCAGCATTTTTTCCCTGACATGAAATATTTCATTTAGAATGCGTATGTTTCCTCTACGTATAAGGTTTCCTAGAGTCAGATATGATAAAAACAAACTCTGAGATGTATATACCTATGTTCCTACAAGTGTAAAACCTGAATGATGTCTCTGGAAATGGAGCCTCGGAGTGACCAGGAACACAAATACTTATATGTCAC... | CCCTTGATTCTGTAAGTGGTAGTTCTAACTTTGAAATGGGTCATCTAACTTATAACTATTTTCTTCATTTCTTTTTAAAAGGGAGAAATAGCATGCAAATTTCTGGCATGTTGATAGAAAGTTCAGCATTTTTTCCCTGACATGAAATATTTCATTTAGAATGCGTATGTTTCCTCTACGTATAAGGTTTCCTAGAGTCAGATATGATAAAAACAAACTCTGAGATGTATATACCTATGTTCCTACAAGTGTAAAACCTGAATGATGTCTCTGGAAATGGAGCCTCGGAGTGACCAGGAACACAAATACTTATATGTCAC... |
Task1_train_39131 | Chromosome 9 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | ACAACCCAGGATATCCCGAAAGCTTGGAGGCATATGGCTGGAAAATGAAACGACCCAGGACATCGTTTCTGGCTGCATCATTATTTTGTGTCGCGTAGTACCAGATGGGCAGTCAGTGAGCGGCGCAGGGATGTGAACGGACGGTTTTATAATGTGAAAATTTTCCCTTGGTAAAGCTAAAACAGATTTAATTTCCCTCTCTTTTCTTTCACTACTTCCCCCTCTTTATTCCCCCTCTGTCTGCAATATCAGTGAACTCAACTTTGCAGTGAGGTGGCCAAAAAGAGAGAGAATGAGGAGATCTTGATCATCTTAGTGTC... | ACAACCCAGGATATCCCGAAAGCTTGGAGGCATATGGCTGGAAAATGAAACGACCCAGGACATCGTTTCTGGCTGCATCATTATTTTGTGTCGCGTAGTACCAGATGGGCAGTCAGTGAGCGGCGCAGGGATGTGAACGGACGGTTTTATAATGTGAAAATTTTCCCTTGGTAAAGCTAAAACAGATTTAATTTCCCTCTCTTTTCTTTCACTACTTCCCCCTCTTTATTCCCCCTCTGTCTGCAATATCAGTGAACTCAACTTTGCAGTGAGGTGGCCAAAAAGAGAGAGAATGAGGAGATCTTGATCATCTTAGTGTC... |
Task1_train_39132 | Assess the clinical impact of this variant found on Chromosome 9. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TCTCCCAGTGCATTATCATTTCTTTGCATTTTTTGGACCTCCTGACTGCCAAGGACTCATCCAGCATCCACTCTATGATCTCAAGACTTCCCTCATAGATAAGAGTCTGTGAGGCTTCATTTCATGTGTCAACTTTGCAGGGTGTGTATTAGATGGGATTACGTTTACATCAGTACATTTTGAGTAAAGAGATCACCCTCCATAATGCAAGTGGGCTTCAACCAATCAGTTGTAGGCTTTAAGAGAAAAGACTGAAGCCCCCCAAAAAGGAAGGAATGTTGCCTCCAGACTGCCTTTGGGCTAAAGATTGCAACGTTAAC... | TCTCCCAGTGCATTATCATTTCTTTGCATTTTTTGGACCTCCTGACTGCCAAGGACTCATCCAGCATCCACTCTATGATCTCAAGACTTCCCTCATAGATAAGAGTCTGTGAGGCTTCATTTCATGTGTCAACTTTGCAGGGTGTGTATTAGATGGGATTACGTTTACATCAGTACATTTTGAGTAAAGAGATCACCCTCCATAATGCAAGTGGGCTTCAACCAATCAGTTGTAGGCTTTAAGAGAAAAGACTGAAGCCCCCCAAAAAGGAAGGAATGTTGCCTCCAGACTGCCTTTGGGCTAAAGATTGCAACGTTAAC... |
Task1_train_39133 | Here’s a variant located on Chromosome 9. What is the predicted biological effect — harmless or disease-causing? | Benign | TTTATTCTCACCATTCGATTAATATCTAACCTTCATTTCTGAACATCTTTATGCATTCAGTCCTGTGTTCTCCAGCAAGGTCACTGGTTTCTTCAAGACAGTCACTAATGTCTTCAGCAGACTGTCCTGTGGGCATTGACGGAGGGAAGCAGGAAATGAAAGAAGCTAGAAGTTCCAGAAATGCATGTAAAATTAAAAGCCCTGGATCTGATACAAATGTATTAAGCCAAGAAGCACCCAGCCTTCATAAGCAAACAGGAAAAAAAGAACAATCATTGCTCCTCTTGGTAACTCCTTTCCTCCTTCAAGATCATACTTGG... | TTTATTCTCACCATTCGATTAATATCTAACCTTCATTTCTGAACATCTTTATGCATTCAGTCCTGTGTTCTCCAGCAAGGTCACTGGTTTCTTCAAGACAGTCACTAATGTCTTCAGCAGACTGTCCTGTGGGCATTGACGGAGGGAAGCAGGAAATGAAAGAAGCTAGAAGTTCCAGAAATGCATGTAAAATTAAAAGCCCTGGATCTGATACAAATGTATTAAGCCAAGAAGCACCCAGCCTTCATAAGCAAACAGGAAAAAAAGAACAATCATTGCTCCTCTTGGTAACTCCTTTCCTCCTTCAAGATCATACTTGG... |
Task1_train_39134 | A variant was discovered on Chromosome 9. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GCAGTTTCCGGGAGAAGGAAAGAGGTGATATGCCCAAGGACACACATGGAAGAGAAAGAGAGTGTTATTACTTCCTATCCACAGGAGAGAAGGAAAGAGGAAGCACAGAAAAGGGAGGGTTTTTGAAGCAGGGTTGAAGGAGGTTTGATGATTCTGTAGATGTAGCTATTCCAGTGAGTTTAGTAACAAGAGCATGGCCTTTGGAGTCAAATGGAGTTGAGTGGGTGCCTAGTGTAAGCTCTTTTACCTCTCTGGTCTCAGTTTTCCTCAGTCAGGATAATAATATGCATTTTCCACAATTTTGGTGAGGATTTAATGAA... | GCAGTTTCCGGGAGAAGGAAAGAGGTGATATGCCCAAGGACACACATGGAAGAGAAAGAGAGTGTTATTACTTCCTATCCACAGGAGAGAAGGAAAGAGGAAGCACAGAAAAGGGAGGGTTTTTGAAGCAGGGTTGAAGGAGGTTTGATGATTCTGTAGATGTAGCTATTCCAGTGAGTTTAGTAACAAGAGCATGGCCTTTGGAGTCAAATGGAGTTGAGTGGGTGCCTAGTGTAAGCTCTTTTACCTCTCTGGTCTCAGTTTTCCTCAGTCAGGATAATAATATGCATTTTCCACAATTTTGGTGAGGATTTAATGAA... |
Task1_train_39135 | Here is a genetic alteration on Chromosome 9. Based on the data, is it a benign variant or a cause of disease? | Benign | AAAATTTTAAACAATGTATTCTATTATTTGTAGCATGTGGTTTATTGATTTGGTAATATCATCATTTATGTCCTAGAATGTATTTCTTTGCAATTGATAAAAGCTGAGAAATATATAAATGCATTTTTTTCTTTTTTTTTATTATTATTATACTTTAAGTTTTAGGGTACATGTGCACAATGTGCAGGTTAGTTACATATGTATACATGTGCCATGCTGGTGTGCTGCACCCATTAACTCATCATTTCGCACTAGATATATCTCCTAATGCTATCCCTCCCCCCTCCCCCCACCCCACAACAGTCCCCAGAGTGTGATGT... | AAAATTTTAAACAATGTATTCTATTATTTGTAGCATGTGGTTTATTGATTTGGTAATATCATCATTTATGTCCTAGAATGTATTTCTTTGCAATTGATAAAAGCTGAGAAATATATAAATGCATTTTTTTCTTTTTTTTTATTATTATTATACTTTAAGTTTTAGGGTACATGTGCACAATGTGCAGGTTAGTTACATATGTATACATGTGCCATGCTGGTGTGCTGCACCCATTAACTCATCATTTCGCACTAGATATATCTCCTAATGCTATCCCTCCCCCCTCCCCCCACCCCACAACAGTCCCCAGAGTGTGATGT... |
Task1_train_39136 | Mutation context: Chromosome 9. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TGTAGCATGTGGTTTATTGATTTGGTAATATCATCATTTATGTCCTAGAATGTATTTCTTTGCAATTGATAAAAGCTGAGAAATATATAAATGCATTTTTTTCTTTTTTTTTATTATTATTATACTTTAAGTTTTAGGGTACATGTGCACAATGTGCAGGTTAGTTACATATGTATACATGTGCCATGCTGGTGTGCTGCACCCATTAACTCATCATTTCGCACTAGATATATCTCCTAATGCTATCCCTCCCCCCTCCCCCCACCCCACAACAGTCCCCAGAGTGTGATGTTCCCCTTCCTGTGTCCATGTGTTCTCAT... | TGTAGCATGTGGTTTATTGATTTGGTAATATCATCATTTATGTCCTAGAATGTATTTCTTTGCAATTGATAAAAGCTGAGAAATATATAAATGCATTTTTTTCTTTTTTTTTATTATTATTATACTTTAAGTTTTAGGGTACATGTGCACAATGTGCAGGTTAGTTACATATGTATACATGTGCCATGCTGGTGTGCTGCACCCATTAACTCATCATTTCGCACTAGATATATCTCCTAATGCTATCCCTCCCCCCTCCCCCCACCCCACAACAGTCCCCAGAGTGTGATGTTCCCCTTCCTGTGTCCATGTGTTCTCAT... |
Task1_train_39137 | A genomic variant on Chromosome 9 is under review. What is the biological outcome — benign or pathogenic? | Benign | CTGGGTAAAAAAAAAATCACAAACACTTGTCAAAAAATTGGCTGTGCCTCTGTTTGGCTTTTAAAGACCATCCTCTTGTGTTTAAAAAGAAACAATAAACAGATTGTTTTCCCAAAATGCACTGCCTATTGTCATGGATGGAAGATAGGGTTGGGGTTTTTTCCCCACAAATTTGCTTTTCAGACAAAAAAAGTAACTCAGAAAGTTTTGTCTCTCTGTAAGTCTGCCAACAAAGAAAACTGTCCTTTTTGAAGCTGCAATAACATACTGCTCTTTATTCAGATCCCAAAGGCCATTATGAGGACTAAGTGGGAAAACGA... | CTGGGTAAAAAAAAAATCACAAACACTTGTCAAAAAATTGGCTGTGCCTCTGTTTGGCTTTTAAAGACCATCCTCTTGTGTTTAAAAAGAAACAATAAACAGATTGTTTTCCCAAAATGCACTGCCTATTGTCATGGATGGAAGATAGGGTTGGGGTTTTTTCCCCACAAATTTGCTTTTCAGACAAAAAAAGTAACTCAGAAAGTTTTGTCTCTCTGTAAGTCTGCCAACAAAGAAAACTGTCCTTTTTGAAGCTGCAATAACATACTGCTCTTTATTCAGATCCCAAAGGCCATTATGAGGACTAAGTGGGAAAACGA... |
Task1_train_39138 | A mutation located on Chromosome 9 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TACAGGGGACCACCCGTTTTTAAAACCATCAGATCCCGTGAGACTTATTCACTATCATGAGAACAGCACAGGAAAAACCCACCCCCATGATTCAATTACCTCCCACCAGGTTCCTCCCATGACACGTGGGAATTGTGGGAGTTACAATTCAAGATGAGATTTGGGTGGGGACACAGCCAAACCATATCAGTAGGTGATTACTTAATTTCAGCTGTCCTTTTTTAAAATCTCTATTATCAACCAGCCTCTCCTTTCAAGGAGTCTACTCTATTATAGTTGTCCAGACACTACCCTGACTCCACTTTCTGTAATTTCTATAT... | TACAGGGGACCACCCGTTTTTAAAACCATCAGATCCCGTGAGACTTATTCACTATCATGAGAACAGCACAGGAAAAACCCACCCCCATGATTCAATTACCTCCCACCAGGTTCCTCCCATGACACGTGGGAATTGTGGGAGTTACAATTCAAGATGAGATTTGGGTGGGGACACAGCCAAACCATATCAGTAGGTGATTACTTAATTTCAGCTGTCCTTTTTTAAAATCTCTATTATCAACCAGCCTCTCCTTTCAAGGAGTCTACTCTATTATAGTTGTCCAGACACTACCCTGACTCCACTTTCTGTAATTTCTATAT... |
Task1_train_39139 | A genomic change on Chromosome 9 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TTGGTTGCCAGTGTATCAGGCAATCTGGACTTTCCAATGACACCACTGAGATGGCACTCCTCAAAATAGCAGCCCTTCTGTTTCTAGATTGTAGATCTTTAGATAAATCCTGCCATTTTCATTTCACTTCCTAAAAGTCAGAGTCTGCTTGTGAAAAGTTGTTAAACAACATGTTAATGTGAAATGTCAACCCCCACTCTAAACTCTCTGTTGAGAACATCAAATGAGGACTTCATTGGGTTTATAGTGGCTTTCTGATTTTGGTAGTCCTTTGAAGAAGAGGGTTTGAAAGTTGTATACTGTTAATTGAAATACCTGCC... | TTGGTTGCCAGTGTATCAGGCAATCTGGACTTTCCAATGACACCACTGAGATGGCACTCCTCAAAATAGCAGCCCTTCTGTTTCTAGATTGTAGATCTTTAGATAAATCCTGCCATTTTCATTTCACTTCCTAAAAGTCAGAGTCTGCTTGTGAAAAGTTGTTAAACAACATGTTAATGTGAAATGTCAACCCCCACTCTAAACTCTCTGTTGAGAACATCAAATGAGGACTTCATTGGGTTTATAGTGGCTTTCTGATTTTGGTAGTCCTTTGAAGAAGAGGGTTTGAAAGTTGTATACTGTTAATTGAAATACCTGCC... |
Task1_train_39140 | This variant is found on Chromosome 9. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | ACTTGATGGTCAAGTGGATTGAAAAGGACAGAATGGTCTCATGGCAAGGAGTGGTAATTTAAAACAACACATTGAAGATAGAAGAGGTACAAAAATATATGTTCACAAGACCCAGCGCATAGAGGGATGTTAATAAATAGAAATATAACTGGAGTGCTGAGAGGAGACTGTTAGATTAGATGTTTTGAAAGCTGAGGGTTTGGTTGTAATAGCACAATGTGGAGAGTTCGGCAGCTGTTAAACAGCGAGTAAAAAGTTGAGTGTTCTGTATAATCCCAGCACTATGCAAGTATCAGTGACATATTAGATATACCTTTTAC... | ACTTGATGGTCAAGTGGATTGAAAAGGACAGAATGGTCTCATGGCAAGGAGTGGTAATTTAAAACAACACATTGAAGATAGAAGAGGTACAAAAATATATGTTCACAAGACCCAGCGCATAGAGGGATGTTAATAAATAGAAATATAACTGGAGTGCTGAGAGGAGACTGTTAGATTAGATGTTTTGAAAGCTGAGGGTTTGGTTGTAATAGCACAATGTGGAGAGTTCGGCAGCTGTTAAACAGCGAGTAAAAAGTTGAGTGTTCTGTATAATCCCAGCACTATGCAAGTATCAGTGACATATTAGATATACCTTTTAC... |
Task1_train_39141 | Mutation context: Chromosome 9. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | ACTTTCTTAAAATAGTCACTGTTCTCAATATAAAATGTTAGGTTTAGCTTTATTATTTTAAAGAAAGATGAAAAGTTGTTTATTTTAAAATTTTAATGGTTTTGCTTTCAAATTATGGAAATTCTCCTTTGGGGACATATTTATTTGAATTATATGTGACATTATTTTTATTTCTTAAGGCTATGATTAAAAGTTTCATGGATGTCTACCAGCTTGCAAGCACTAGAATCATGACATTAGAGAAGGAAATGACATCTCATCGAAGTCACATTGCAGCCTTGAAATCAGAACTTCACACAGCTTGTTTACGTGAAAATGCA... | ACTTTCTTAAAATAGTCACTGTTCTCAATATAAAATGTTAGGTTTAGCTTTATTATTTTAAAGAAAGATGAAAAGTTGTTTATTTTAAAATTTTAATGGTTTTGCTTTCAAATTATGGAAATTCTCCTTTGGGGACATATTTATTTGAATTATATGTGACATTATTTTTATTTCTTAAGGCTATGATTAAAAGTTTCATGGATGTCTACCAGCTTGCAAGCACTAGAATCATGACATTAGAGAAGGAAATGACATCTCATCGAAGTCACATTGCAGCCTTGAAATCAGAACTTCACACAGCTTGTTTACGTGAAAATGCA... |
Task1_train_39142 | This genomic variant is located on Chromosome 9. Can you determine its pathogenicity and name any linked disease? | Benign | GATCTTTAATTCCTGTTTTTATCTTGCAACTCCACAGACACTTATCAACAGGTCCTGTCATTTTTACCTTCAGAATATATTTTAAATTTGACTCTTCATCACCTCTGTTATTACTTATCAAGCCACCATCAGCTTTGGCTGGATTATTTTCAATAATTTTTGATTTGGTTCCTCTATGTCTACTCTTCACGTAAAATAGTAGTTTTTTCATTTTAGCTGCCTGGTTGTTCCATTTTTGCTTCATAATATTTGTCTATTTTAGTATATTCTGTATATTTATAGTCCTTTTGAATTGGTTCCCATATTTGCATTTTGCTAGG... | GATCTTTAATTCCTGTTTTTATCTTGCAACTCCACAGACACTTATCAACAGGTCCTGTCATTTTTACCTTCAGAATATATTTTAAATTTGACTCTTCATCACCTCTGTTATTACTTATCAAGCCACCATCAGCTTTGGCTGGATTATTTTCAATAATTTTTGATTTGGTTCCTCTATGTCTACTCTTCACGTAAAATAGTAGTTTTTTCATTTTAGCTGCCTGGTTGTTCCATTTTTGCTTCATAATATTTGTCTATTTTAGTATATTCTGTATATTTATAGTCCTTTTGAATTGGTTCCCATATTTGCATTTTGCTAGG... |
Task1_train_39143 | Chromosome 9 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CTGAATTTAAGTAACTAGATCAAAGTAAAATTTAGTTAACTTTGAGCAGCTAGATTTGAACTCTTATCAACACAGCATCCTACGTGTAATAGACTCTTCATGTATGGTTCTTAAATTGAAATGAACAAAATTGAACTCAGTAACCTGAGGTTTTTACTTTTACTTCATATATTAAACTATCCTACTTTAGCAAATTTGCATTATGTGTGATTTGTATATCTTCTAAAACTACTTAGGAAACATTTATTTTGAATGCCTTTGTCAACTGAATCCATTCTGCTTTTTCATCAAGCACTTTCATTTCTGTACGGCATATAGAA... | CTGAATTTAAGTAACTAGATCAAAGTAAAATTTAGTTAACTTTGAGCAGCTAGATTTGAACTCTTATCAACACAGCATCCTACGTGTAATAGACTCTTCATGTATGGTTCTTAAATTGAAATGAACAAAATTGAACTCAGTAACCTGAGGTTTTTACTTTTACTTCATATATTAAACTATCCTACTTTAGCAAATTTGCATTATGTGTGATTTGTATATCTTCTAAAACTACTTAGGAAACATTTATTTTGAATGCCTTTGTCAACTGAATCCATTCTGCTTTTTCATCAAGCACTTTCATTTCTGTACGGCATATAGAA... |
Task1_train_39144 | A sequence alteration has been identified on Chromosome 9. Is it disease-inducing or harmless? | Benign | TTGATTTAAGAAAGAAACTTTTACATGAGCATGACAAATCCATATGGATTTTCTTTCTCTTCTCTTCCACACATCTGTGCAAGTTAAAATCACTTCCTATAGGCTTTTTCAATGTTATCCTTTCAATTTTGCTATTTTTTAACTTCAATAATAATTTCATACATAGCCTTGGAATCTTTATATAAATAACATATATCTTTAGTGGCATTAAACTGAAAAACTATTTTTTCTGTTATGCTTTGAGTTACATACACATATTATAATCTTATAAATAAGCTATATATATATATAAAATATCCTATTGTTTTATTTCATCCAAA... | TTGATTTAAGAAAGAAACTTTTACATGAGCATGACAAATCCATATGGATTTTCTTTCTCTTCTCTTCCACACATCTGTGCAAGTTAAAATCACTTCCTATAGGCTTTTTCAATGTTATCCTTTCAATTTTGCTATTTTTTAACTTCAATAATAATTTCATACATAGCCTTGGAATCTTTATATAAATAACATATATCTTTAGTGGCATTAAACTGAAAAACTATTTTTTCTGTTATGCTTTGAGTTACATACACATATTATAATCTTATAAATAAGCTATATATATATATAAAATATCCTATTGTTTTATTTCATCCAAA... |
Task1_train_39145 | Chromosome 9 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CTTAAAAAGGCATGAAGTACTGAAACATGCTACAATATGGATGAACCTTCAAGACATTATGCTAAGTGAAATAAGTCAAACACAAAAGGACAAATACCCTGATTCCACTTATTTGAGATTAGTTAAGTTCATAGAGACAGAAAGTAGAATGGTGGTTGTCAAGGGCTGGTGGAACGAGGGGAATGGGGAGTTACTGTTTAATATACGTGGAATTTCAGTTTGGAAAGATGAAAAATCCTAGAGATAGAGGTGGTGATGGTTACACAACAACATGAATGTAATTAATGCCACTGAGTAAGTGACTTAAAAATGATTCAAAT... | CTTAAAAAGGCATGAAGTACTGAAACATGCTACAATATGGATGAACCTTCAAGACATTATGCTAAGTGAAATAAGTCAAACACAAAAGGACAAATACCCTGATTCCACTTATTTGAGATTAGTTAAGTTCATAGAGACAGAAAGTAGAATGGTGGTTGTCAAGGGCTGGTGGAACGAGGGGAATGGGGAGTTACTGTTTAATATACGTGGAATTTCAGTTTGGAAAGATGAAAAATCCTAGAGATAGAGGTGGTGATGGTTACACAACAACATGAATGTAATTAATGCCACTGAGTAAGTGACTTAAAAATGATTCAAAT... |
Task1_train_39146 | A sequence alteration has been identified on Chromosome 9. Is it disease-inducing or harmless? | Benign | CTGAAACTCTGTTTTTATGTTTCTACTTAGCAGCCTTAAAACGACCATGCTCTTTTAAATTTTCAGGCTTCTTACTTCCATCCCACCTGATCCTTGGATTTAGCGCTGTCATTTACAATAAAATAAGGAATGGGTGGAATCTGGAACCCATAATTTTCAGACTATAAAAGCAATGGGTTTGATTCTCACCACTATCCTTTGCATCTTAAATTTCTTTCAGGGTAGCATATATCACAGCACATCACACAGAATAGTGTCACTTCAATATGTTAGCATATAACACTTGAAAATATAAGATCATTTTTTGTTTGTTTTTTAAC... | CTGAAACTCTGTTTTTATGTTTCTACTTAGCAGCCTTAAAACGACCATGCTCTTTTAAATTTTCAGGCTTCTTACTTCCATCCCACCTGATCCTTGGATTTAGCGCTGTCATTTACAATAAAATAAGGAATGGGTGGAATCTGGAACCCATAATTTTCAGACTATAAAAGCAATGGGTTTGATTCTCACCACTATCCTTTGCATCTTAAATTTCTTTCAGGGTAGCATATATCACAGCACATCACACAGAATAGTGTCACTTCAATATGTTAGCATATAACACTTGAAAATATAAGATCATTTTTTGTTTGTTTTTTAAC... |
Task1_train_39147 | This alteration occurs on Chromosome 9. Is it associated with a disease or is it a benign variant? | Benign | AATGCATTTGGGATTTTCCCCTCATTTGAATGACAGCTCTTTGAGATTAGGAACTATTCTTGCACATCTTTTCTTCTTAACATCTAGCACCCTACCTTAGACAAAGTAGATTCATAACTACCTAATGCTTGACACTAAAATATTGTCACTTACTTGTGAAGGAAGGAAAAAGGAATTAGCAATAATTGTCATTTCTATGTATGGCATTTAAAATATATTATCTCACTTAATTCCCAGGCTTGCAAACTAAGCATAAGTGGAAACAGACGAGAGAATTTAAGTAACTTGCCAACTAGTGAAATACTGAGCTGGGATTTAAA... | AATGCATTTGGGATTTTCCCCTCATTTGAATGACAGCTCTTTGAGATTAGGAACTATTCTTGCACATCTTTTCTTCTTAACATCTAGCACCCTACCTTAGACAAAGTAGATTCATAACTACCTAATGCTTGACACTAAAATATTGTCACTTACTTGTGAAGGAAGGAAAAAGGAATTAGCAATAATTGTCATTTCTATGTATGGCATTTAAAATATATTATCTCACTTAATTCCCAGGCTTGCAAACTAAGCATAAGTGGAAACAGACGAGAGAATTTAAGTAACTTGCCAACTAGTGAAATACTGAGCTGGGATTTAAA... |
Task1_train_39148 | Assess the clinical impact of this variant found on Chromosome 9. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | AGGAAAGTTTGTTAGCTTTTAGCAGGTACTTTATGAACATCAAAGCAATGTCTCATTTAATCTGCAAAAATGTAGCTTAATTTTTAAAGGGGGCATTTTGTGGATGAAACTGAGATTTCACCCCAAGTTCCGTGACTTAACCTGTACTATGAGGACTTGAAATGCAGTAAGGCAGACTTTCATCCATGTATTCATATAGTCCATTGGACAGATATTCATTAAGTGTTGCCATTTTATGTTGCTGACATTAAGTTCCATGTCACCTGGACACTGGTAAAGTTTTAGGAGAAATATAAGTGGTGGCCTCTACCCCTGGAGAA... | AGGAAAGTTTGTTAGCTTTTAGCAGGTACTTTATGAACATCAAAGCAATGTCTCATTTAATCTGCAAAAATGTAGCTTAATTTTTAAAGGGGGCATTTTGTGGATGAAACTGAGATTTCACCCCAAGTTCCGTGACTTAACCTGTACTATGAGGACTTGAAATGCAGTAAGGCAGACTTTCATCCATGTATTCATATAGTCCATTGGACAGATATTCATTAAGTGTTGCCATTTTATGTTGCTGACATTAAGTTCCATGTCACCTGGACACTGGTAAAGTTTTAGGAGAAATATAAGTGGTGGCCTCTACCCCTGGAGAA... |
Task1_train_39149 | This genomic variant is located on Chromosome 9. Can you determine its pathogenicity and name any linked disease? | Benign | GGCAGCTAACAAAGCAACCTGCAACAACCAACCTTCAAAGCATCCCTGTCTATACTTTCAGGATAGGAAATATATCAGTGTCTGAAGCCAACTAGACATCTCACAAAGTCTTCTTCATTTCCTGCAAATTGGATATAAAGAGATAAAAAGACCCACACCTGGAGACCGAACAAGATATTTGCAAGCCACCCCTCAGTACTACTCTCACCCTTTCCTACCGATTACATGTCCCTTATACATGTGCCTAGGACTCTTACTTGGTGTTGACCAGGGTTTCCTAAAACAAAAGCAATGCTCAGAAATGGTTCACACTTCTTATT... | GGCAGCTAACAAAGCAACCTGCAACAACCAACCTTCAAAGCATCCCTGTCTATACTTTCAGGATAGGAAATATATCAGTGTCTGAAGCCAACTAGACATCTCACAAAGTCTTCTTCATTTCCTGCAAATTGGATATAAAGAGATAAAAAGACCCACACCTGGAGACCGAACAAGATATTTGCAAGCCACCCCTCAGTACTACTCTCACCCTTTCCTACCGATTACATGTCCCTTATACATGTGCCTAGGACTCTTACTTGGTGTTGACCAGGGTTTCCTAAAACAAAAGCAATGCTCAGAAATGGTTCACACTTCTTATT... |
Task1_train_39150 | Consider a variant on Chromosome 9. Determine its clinical classification and disease relevance. | Benign | TCTTCTTCATTTCCTGCAAATTGGATATAAAGAGATAAAAAGACCCACACCTGGAGACCGAACAAGATATTTGCAAGCCACCCCTCAGTACTACTCTCACCCTTTCCTACCGATTACATGTCCCTTATACATGTGCCTAGGACTCTTACTTGGTGTTGACCAGGGTTTCCTAAAACAAAAGCAATGCTCAGAAATGGTTCACACTTCTTATTATGGTCTTTAGACTCTCAGAGACAAAGAATACTGTTTTCCCAGCAAAATGAAGCCCAAACTTTAGTGTTCATATTGTTTAATAAGTCATAGGTTGAAAAAACAGCAGC... | TCTTCTTCATTTCCTGCAAATTGGATATAAAGAGATAAAAAGACCCACACCTGGAGACCGAACAAGATATTTGCAAGCCACCCCTCAGTACTACTCTCACCCTTTCCTACCGATTACATGTCCCTTATACATGTGCCTAGGACTCTTACTTGGTGTTGACCAGGGTTTCCTAAAACAAAAGCAATGCTCAGAAATGGTTCACACTTCTTATTATGGTCTTTAGACTCTCAGAGACAAAGAATACTGTTTTCCCAGCAAAATGAAGCCCAAACTTTAGTGTTCATATTGTTTAATAAGTCATAGGTTGAAAAAACAGCAGC... |
Task1_train_39151 | The following genetic variant occurs on Chromosome 9. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CATTACAAAGAAAAATAAACAATAGATTCCAAGCAATAGCAAATTTTAGTCAATACAAAAAAGGTTCATAGCTTTGCAAATACTTGATTATGATAAAATTATTATTATTCTCACCAAAGTACCCTCTTTCTCCAGAGATCAATACATTCCTCCCAGAGTACTTTTTTTTTTTTCTTTTTTCTGCGACAGGGTCTTGCTCTGTCACCCAGGCTGGAGTGCAGTGGCACGATCGCAGCTCACTTCAGCCTCAAACTCCCAGGCCCAAGCAATCCTCCCACCTCAGCCTCCTGTGTACCTGGGATCACAGGCATGCGCCAACG... | CATTACAAAGAAAAATAAACAATAGATTCCAAGCAATAGCAAATTTTAGTCAATACAAAAAAGGTTCATAGCTTTGCAAATACTTGATTATGATAAAATTATTATTATTCTCACCAAAGTACCCTCTTTCTCCAGAGATCAATACATTCCTCCCAGAGTACTTTTTTTTTTTTCTTTTTTCTGCGACAGGGTCTTGCTCTGTCACCCAGGCTGGAGTGCAGTGGCACGATCGCAGCTCACTTCAGCCTCAAACTCCCAGGCCCAAGCAATCCTCCCACCTCAGCCTCCTGTGTACCTGGGATCACAGGCATGCGCCAACG... |
Task1_train_39152 | A variant was discovered on Chromosome 9. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CCCAAGCAATCCTCCCACCTCAGCCTCCTGTGTACCTGGGATCACAGGCATGCGCCAACGTGCCCAGCTAATTGTTTAATTTTTTGTAGAGACATAGTCTCCCTGTGTTGCTGAGGCTAGTCTCGAACTCCTGGGTTCAAGTGATCCTCCCATCTCGGACTCCCAAAGTGCTGGGATTGCAGGTGTGAGCCACTGTGCCCAGCCAAATACTTTTCAATATGGCAGTGTATAACTATTATGGGCAAATCAGAGTATGTAATGAATCTGTATCACCAGATCCTTATCTCTCTTAATGAGCTACAAGAGCAATTTTTTTAACC... | CCCAAGCAATCCTCCCACCTCAGCCTCCTGTGTACCTGGGATCACAGGCATGCGCCAACGTGCCCAGCTAATTGTTTAATTTTTTGTAGAGACATAGTCTCCCTGTGTTGCTGAGGCTAGTCTCGAACTCCTGGGTTCAAGTGATCCTCCCATCTCGGACTCCCAAAGTGCTGGGATTGCAGGTGTGAGCCACTGTGCCCAGCCAAATACTTTTCAATATGGCAGTGTATAACTATTATGGGCAAATCAGAGTATGTAATGAATCTGTATCACCAGATCCTTATCTCTCTTAATGAGCTACAAGAGCAATTTTTTTAACC... |
Task1_train_39153 | A genomic change on Chromosome 9 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GCAGGTGTGAGCCACTGTGCCCAGCCAAATACTTTTCAATATGGCAGTGTATAACTATTATGGGCAAATCAGAGTATGTAATGAATCTGTATCACCAGATCCTTATCTCTCTTAATGAGCTACAAGAGCAATTTTTTTAACCTTTTATGAGGAAAACATTCAAACATACAAAAGTGAAGAGAACTGTGATTAACTCAATATATCCATCACCTAGCTTCAATAATTATTAATACTAACTGTTATGAACTGAATACCCCCAAAAACATATGTTGAAGTTCTAACCCCAGTACCTCAGAATGTGACCTTATTTGGAAATGTGG... | GCAGGTGTGAGCCACTGTGCCCAGCCAAATACTTTTCAATATGGCAGTGTATAACTATTATGGGCAAATCAGAGTATGTAATGAATCTGTATCACCAGATCCTTATCTCTCTTAATGAGCTACAAGAGCAATTTTTTTAACCTTTTATGAGGAAAACATTCAAACATACAAAAGTGAAGAGAACTGTGATTAACTCAATATATCCATCACCTAGCTTCAATAATTATTAATACTAACTGTTATGAACTGAATACCCCCAAAAACATATGTTGAAGTTCTAACCCCAGTACCTCAGAATGTGACCTTATTTGGAAATGTGG... |
Task1_train_39154 | This variant is located on Chromosome 9. Evaluate its biological effect and specify any disease association. | Benign | GCTAATTTTTGTATTTTTTTGCGGAGACAGGGTTTCTCCATGTTGCCCAGGCTGGTCTCGAGCTCCTGAGCTCAGGTGATCCGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCATGCCCGGCATAACCCTAACTTAAAAAAAAATAAAAGAAAGAAATTTATTTCTTATAGTTCTAGGGGCTGGAAAGTCCAGGGTTAGGGTGTTAGCATGGTGAGTTCTGCAGAGGGCCCTCTTCCAGGTTGCAGAGTGCTAACTTATTGTATCCTCGTACAGCAGAGAAGGAGAGAGCTCTCCTTTAAGGGC... | GCTAATTTTTGTATTTTTTTGCGGAGACAGGGTTTCTCCATGTTGCCCAGGCTGGTCTCGAGCTCCTGAGCTCAGGTGATCCGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCATGCCCGGCATAACCCTAACTTAAAAAAAAATAAAAGAAAGAAATTTATTTCTTATAGTTCTAGGGGCTGGAAAGTCCAGGGTTAGGGTGTTAGCATGGTGAGTTCTGCAGAGGGCCCTCTTCCAGGTTGCAGAGTGCTAACTTATTGTATCCTCGTACAGCAGAGAAGGAGAGAGCTCTCCTTTAAGGGC... |
Task1_train_39155 | This sequence change occurs on Chromosome 9. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GACCACGCTTGTATTATACGGATTATTTCCAGGGCTATGATTATGGGCAACTGCCACCTATTTGTCAATTGCTTTTTTTTTTTTTTTTGCAACATCAGCTTCATAAGGGTAGGAATTTGTCTATACTGTATTCTCAGCACCTTGAACAGTACCTGTGCTCAAGTAAGTGTAATTACTGACTTAACAGACGTATACTATCTATGCCATGTATGTTAAGTCACACCAGTCCTGAAAACCAAAATCCAGAGAAATTCTTTCAAATTTTGTCAGGAAAACCCAACCTTGACTGACATGCTGTTTATTTAACATAAATATCCCCA... | GACCACGCTTGTATTATACGGATTATTTCCAGGGCTATGATTATGGGCAACTGCCACCTATTTGTCAATTGCTTTTTTTTTTTTTTTTGCAACATCAGCTTCATAAGGGTAGGAATTTGTCTATACTGTATTCTCAGCACCTTGAACAGTACCTGTGCTCAAGTAAGTGTAATTACTGACTTAACAGACGTATACTATCTATGCCATGTATGTTAAGTCACACCAGTCCTGAAAACCAAAATCCAGAGAAATTCTTTCAAATTTTGTCAGGAAAACCCAACCTTGACTGACATGCTGTTTATTTAACATAAATATCCCCA... |
Task1_train_39156 | A sequence alteration has been identified on Chromosome 9. Is it disease-inducing or harmless? | Benign | TCCCACCCTCTGTTTGGAGTCCCTTGTGTCTGTTGTTCCCACCTTCATGTCTGTGTGAACCCAAGGTTTAGCTCCCACTCTTAAATGAGAACGGTCAAGCATAATTTAAATACCGTTTCTTCCGTGAAGCAATTGCACTTTATACCTTTCTTTTGGCAGTTGTCACTTTCTATCATCTAGTTCAGGATCATAACTGATTGTCTCTGTCAGACTGTATGCTTCTTGAGGATAGATAATTCTTATTTCATCTTTGTATCTTATCTAATCATTCCTTATATATAAGAATGTGAAAAACATTAGAAAATAAAGTCATGACATTT... | TCCCACCCTCTGTTTGGAGTCCCTTGTGTCTGTTGTTCCCACCTTCATGTCTGTGTGAACCCAAGGTTTAGCTCCCACTCTTAAATGAGAACGGTCAAGCATAATTTAAATACCGTTTCTTCCGTGAAGCAATTGCACTTTATACCTTTCTTTTGGCAGTTGTCACTTTCTATCATCTAGTTCAGGATCATAACTGATTGTCTCTGTCAGACTGTATGCTTCTTGAGGATAGATAATTCTTATTTCATCTTTGTATCTTATCTAATCATTCCTTATATATAAGAATGTGAAAAACATTAGAAAATAAAGTCATGACATTT... |
Task1_train_39157 | Given this context: Chromosome 9 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AGTGTCTCTGGGGTGATTGGTCTCCAGTCAAATGCAGTCTGGCTTCTTGGACATCTTCATCTATCTACTCTATCCTCAAGTCAAAGTAGAGCCTCTGGTAAGATTAAAGTCATAAAATACTGGAGCTGGAAGGGAGGGATTGCCGACCCAGCGCTCTGTAGTTTGTTAAGAGCATTAATCTTCACAACAACCCTAAGTAATGGGTATTACCATCTCTGTTTTACGTCAGAGGGAAATGGTGTATGGAAAGGCTTCCTGACTTACCCAGGGTCATGTGACAGTAAGTGATGGACATGTGGTTTGAACTCAGATCTTTTGGC... | AGTGTCTCTGGGGTGATTGGTCTCCAGTCAAATGCAGTCTGGCTTCTTGGACATCTTCATCTATCTACTCTATCCTCAAGTCAAAGTAGAGCCTCTGGTAAGATTAAAGTCATAAAATACTGGAGCTGGAAGGGAGGGATTGCCGACCCAGCGCTCTGTAGTTTGTTAAGAGCATTAATCTTCACAACAACCCTAAGTAATGGGTATTACCATCTCTGTTTTACGTCAGAGGGAAATGGTGTATGGAAAGGCTTCCTGACTTACCCAGGGTCATGTGACAGTAAGTGATGGACATGTGGTTTGAACTCAGATCTTTTGGC... |
Task1_train_39158 | The following genetic variant occurs on Chromosome 9. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CTGTGCAGCACCGTGAGAAAGAGGTGTTGGCCTGGATGATTCTGCACAGCTTATACCAGGCACGGATTGTGAGCCATGCCAATACGGGTGAGGACACCCTGGGGTGAACATCAGAAACAGGAATAGATCTGCCTGCTGTTGCTTTTAAGTTGCACTTGAGTTCTCAACTTAAAAATTAGTTTAGTGCTTATTGACACAGGTTAGGCCTTCTGGTGCCAAATGAGGAGTAACTTGGATAGAAATTAACAGTTATAGCTCACAACATCCACTTTTTGGAAATGAGGATGGATTCTTTCGAGGGGTTTTGTTTTCTATTTGGC... | CTGTGCAGCACCGTGAGAAAGAGGTGTTGGCCTGGATGATTCTGCACAGCTTATACCAGGCACGGATTGTGAGCCATGCCAATACGGGTGAGGACACCCTGGGGTGAACATCAGAAACAGGAATAGATCTGCCTGCTGTTGCTTTTAAGTTGCACTTGAGTTCTCAACTTAAAAATTAGTTTAGTGCTTATTGACACAGGTTAGGCCTTCTGGTGCCAAATGAGGAGTAACTTGGATAGAAATTAACAGTTATAGCTCACAACATCCACTTTTTGGAAATGAGGATGGATTCTTTCGAGGGGTTTTGTTTTCTATTTGGC... |
Task1_train_39159 | This sequence change occurs on Chromosome 9. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TGATCAGGACTTTTGGGGTTTGCATTGCAGAGGGTTCACATGAAATACTGTGCACTTGGAGCTGAAATGGAAGGGAAACAAATGTTCCTCTACATAGGATAAATGTGTTGCTTTAAGTTCTAAAATGAAATCCTGCCATGTTTAGAAACTCGTAGGGAAGATTTTGCTCTCTTTACTGCCCAGTGATGATTCACACAATAATAATTTACTGAGCAGTAAGGATTTCTCTTCTCGGCAGCTCCACAAGATGGACACTATTATCATCATCCCCATTTCAGAGATGGTTCCTGAAGTACACAGTCCATGCTCTTATCCACTGC... | TGATCAGGACTTTTGGGGTTTGCATTGCAGAGGGTTCACATGAAATACTGTGCACTTGGAGCTGAAATGGAAGGGAAACAAATGTTCCTCTACATAGGATAAATGTGTTGCTTTAAGTTCTAAAATGAAATCCTGCCATGTTTAGAAACTCGTAGGGAAGATTTTGCTCTCTTTACTGCCCAGTGATGATTCACACAATAATAATTTACTGAGCAGTAAGGATTTCTCTTCTCGGCAGCTCCACAAGATGGACACTATTATCATCATCCCCATTTCAGAGATGGTTCCTGAAGTACACAGTCCATGCTCTTATCCACTGC... |
Task1_train_39160 | Here is a mutation located on Chromosome 9. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AGACCTCTGTCAATTGGGTAGACGGCAAAAATTTTCTCCCATTCTGTAAGTTGCCTGTTCACCCTGATGATTGATAGTTTCTTTTGCTGTGCAGAAGCTCTTTAATTAGATGCCATTTGTCAATTTTAGCTTTGGTTGCAGTTGCTTTTGGCAATTTCATCATAAAATCTTTGCCCATGCCAATGTCCTGAATGCTATTGCCTACATTTTCCTCTAGGGTTTTTATGGTTTTGGGATTTACATTTAAGTGTTTAATCAGTCTTGAGTTAATTTTTGTATAAGGTGTAAGGAAGGGGTCCAGTGTCAGTTTCCTGCATATG... | AGACCTCTGTCAATTGGGTAGACGGCAAAAATTTTCTCCCATTCTGTAAGTTGCCTGTTCACCCTGATGATTGATAGTTTCTTTTGCTGTGCAGAAGCTCTTTAATTAGATGCCATTTGTCAATTTTAGCTTTGGTTGCAGTTGCTTTTGGCAATTTCATCATAAAATCTTTGCCCATGCCAATGTCCTGAATGCTATTGCCTACATTTTCCTCTAGGGTTTTTATGGTTTTGGGATTTACATTTAAGTGTTTAATCAGTCTTGAGTTAATTTTTGTATAAGGTGTAAGGAAGGGGTCCAGTGTCAGTTTCCTGCATATG... |
Task1_train_39161 | Chromosome 9 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AATGCTATTGCCTACATTTTCCTCTAGGGTTTTTATGGTTTTGGGATTTACATTTAAGTGTTTAATCAGTCTTGAGTTAATTTTTGTATAAGGTGTAAGGAAGGGGTCCAGTGTCAGTTTCCTGCATATGGTTTTCCAGTTTTCCCAGCACCATTTATTAAATAAGGAATCCCTTCCCCATTCCTAAAGTATTGAGAAAGAGATTCTCTTTTCCAGTTTCTGATTTTATTTTATGAAACAAATGTGTCAGTTTTTACTGACATTTAACGGAATATTAATCAAAATAATGATCAATTACTATTGTAAATTTTATATTTTAT... | AATGCTATTGCCTACATTTTCCTCTAGGGTTTTTATGGTTTTGGGATTTACATTTAAGTGTTTAATCAGTCTTGAGTTAATTTTTGTATAAGGTGTAAGGAAGGGGTCCAGTGTCAGTTTCCTGCATATGGTTTTCCAGTTTTCCCAGCACCATTTATTAAATAAGGAATCCCTTCCCCATTCCTAAAGTATTGAGAAAGAGATTCTCTTTTCCAGTTTCTGATTTTATTTTATGAAACAAATGTGTCAGTTTTTACTGACATTTAACGGAATATTAATCAAAATAATGATCAATTACTATTGTAAATTTTATATTTTAT... |
Task1_train_39162 | A variant was discovered on Chromosome 9. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TGATTGACAGTTTCTTTTGCTGTGCAGAATCTCTTTAATTAGATGCCATTTGTCAATTTTAGCTTTGGTTGCAGTTGCTTTTGGCGATTTCATCATAAAATCTTTGCCCATGCCGATGTCCTGAATGCTATTGCCTACGTTTTCTTCTAGGGTTTTTATGGTTTTGGGTTTTACATTTAAGTGTTTAATCCATCTTGCATTAATTTTTGTATAAGGTGTAAGGAAGGGGTCCAGTTTCAGTTCTCTGCATATGGCTATCCAGTTTTCCCAGCACCATTTATTAAAGAGGGAATCCTTTCCCCATTCCTAAAGTACTCAGA... | TGATTGACAGTTTCTTTTGCTGTGCAGAATCTCTTTAATTAGATGCCATTTGTCAATTTTAGCTTTGGTTGCAGTTGCTTTTGGCGATTTCATCATAAAATCTTTGCCCATGCCGATGTCCTGAATGCTATTGCCTACGTTTTCTTCTAGGGTTTTTATGGTTTTGGGTTTTACATTTAAGTGTTTAATCCATCTTGCATTAATTTTTGTATAAGGTGTAAGGAAGGGGTCCAGTTTCAGTTCTCTGCATATGGCTATCCAGTTTTCCCAGCACCATTTATTAAAGAGGGAATCCTTTCCCCATTCCTAAAGTACTCAGA... |
Task1_train_39163 | Given this variant on Chromosome 9, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TTTTATGGTTTTGGGTTTTACATTTAAGTGTTTAATCCATCTTGCATTAATTTTTGTATAAGGTGTAAGGAAGGGGTCCAGTTTCAGTTCTCTGCATATGGCTATCCAGTTTTCCCAGCACCATTTATTAAAGAGGGAATCCTTTCCCCATTCCTAAAGTACTCAGAAAGAGATTATCTTTTCCAGTTTCCAATTTTATTTTATGAAAAAATGTGTCAGTTTTTACTGACATTTAACAGAGTATTAATCAAAATAATGATCAATTACTATTGTAAATAATTTTACATTTTATGCTTTAAATATATAAATTATTAAATGTA... | TTTTATGGTTTTGGGTTTTACATTTAAGTGTTTAATCCATCTTGCATTAATTTTTGTATAAGGTGTAAGGAAGGGGTCCAGTTTCAGTTCTCTGCATATGGCTATCCAGTTTTCCCAGCACCATTTATTAAAGAGGGAATCCTTTCCCCATTCCTAAAGTACTCAGAAAGAGATTATCTTTTCCAGTTTCCAATTTTATTTTATGAAAAAATGTGTCAGTTTTTACTGACATTTAACAGAGTATTAATCAAAATAATGATCAATTACTATTGTAAATAATTTTACATTTTATGCTTTAAATATATAAATTATTAAATGTA... |
Task1_train_39164 | A variant has been detected on Chromosome 9. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TATGGTTTTGGGTTTTACATTTAAGTGTTTAATCCATCTTGCATTAATTTTTGTATAAGGTGTAAGGAAGGGGTCCAGTTTCAGTTCTCTGCATATGGCTATCCAGTTTTCCCAGCACCATTTATTAAAGAGGGAATCCTTTCCCCATTCCTAAAGTACTCAGAAAGAGATTATCTTTTCCAGTTTCCAATTTTATTTTATGAAAAAATGTGTCAGTTTTTACTGACATTTAACAGAGTATTAATCAAAATAATGATCAATTACTATTGTAAATAATTTTACATTTTATGCTTTAAATATATAAATTATTAAATGTATTA... | TATGGTTTTGGGTTTTACATTTAAGTGTTTAATCCATCTTGCATTAATTTTTGTATAAGGTGTAAGGAAGGGGTCCAGTTTCAGTTCTCTGCATATGGCTATCCAGTTTTCCCAGCACCATTTATTAAAGAGGGAATCCTTTCCCCATTCCTAAAGTACTCAGAAAGAGATTATCTTTTCCAGTTTCCAATTTTATTTTATGAAAAAATGTGTCAGTTTTTACTGACATTTAACAGAGTATTAATCAAAATAATGATCAATTACTATTGTAAATAATTTTACATTTTATGCTTTAAATATATAAATTATTAAATGTATTA... |
Task1_train_39165 | Here is a mutation located on Chromosome 9. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CTCTGCATATGGCTATCCAGTTTTCCCAGCACCATTTATTAAAGAGGGAATCCTTTCCCCATTCCTAAAGTACTCAGAAAGAGATTATCTTTTCCAGTTTCCAATTTTATTTTATGAAAAAATGTGTCAGTTTTTACTGACATTTAACAGAGTATTAATCAAAATAATGATCAATTACTATTGTAAATAATTTTACATTTTATGCTTTAAATATATAAATTATTAAATGTATTAATATGATTCACCAATGCATCACAATTATGAAATTTATTCAGTGACATATATTTTCAAAAAGGAAACACTATGCAGATAAAAGATAA... | CTCTGCATATGGCTATCCAGTTTTCCCAGCACCATTTATTAAAGAGGGAATCCTTTCCCCATTCCTAAAGTACTCAGAAAGAGATTATCTTTTCCAGTTTCCAATTTTATTTTATGAAAAAATGTGTCAGTTTTTACTGACATTTAACAGAGTATTAATCAAAATAATGATCAATTACTATTGTAAATAATTTTACATTTTATGCTTTAAATATATAAATTATTAAATGTATTAATATGATTCACCAATGCATCACAATTATGAAATTTATTCAGTGACATATATTTTCAAAAAGGAAACACTATGCAGATAAAAGATAA... |
Task1_train_39166 | A sequence alteration has been identified on Chromosome 9. Is it disease-inducing or harmless? | Benign | GATGATGACCTGATCCCTCAGGAACAGATGGTGTTTCAGCTTTGTGGGAGTGACTGTCAAGGTATGGAGCACTTAGGTGGTCTTTGAAACCTGTCAGGTTTCACATCTCTGCTTTGAGTGAAAAGCTCATCACCCACAGTAGTGAGGAATGTGCCTATACTTGCTGGGGCTGATCTGTTGAAACTTTATGTGTAGACAATGGAAACATCCAGGAGCATTTCTGCTTTCATGTAGCCTCTTAATAATTGATGTCCCTGAAGTCCTGTGTCCTCAGGGACAGTTCCTCTGATTCCTGGATTGTACCAGCTTTCATGATGTTA... | GATGATGACCTGATCCCTCAGGAACAGATGGTGTTTCAGCTTTGTGGGAGTGACTGTCAAGGTATGGAGCACTTAGGTGGTCTTTGAAACCTGTCAGGTTTCACATCTCTGCTTTGAGTGAAAAGCTCATCACCCACAGTAGTGAGGAATGTGCCTATACTTGCTGGGGCTGATCTGTTGAAACTTTATGTGTAGACAATGGAAACATCCAGGAGCATTTCTGCTTTCATGTAGCCTCTTAATAATTGATGTCCCTGAAGTCCTGTGTCCTCAGGGACAGTTCCTCTGATTCCTGGATTGTACCAGCTTTCATGATGTTA... |
Task1_train_39167 | This mutation occurs on Chromosome 9. Does this change lead to a known medical condition, or is it benign? | Benign | GGCATCCTTATCTTATAATAAATCTCAGAAAAAAGATTCCAACATTTCACCACTGACTATAGTGTTAGCTAATGGCTTATCTTATAGCTAATAAGGAATGTGTCTCTTTATTCTGAGGTATATTCTTTATATACCTAATTTGTTATAAATTGTATTAGAGATGGATTTTAAATTTTGTCAAAATAATTTTAGGCATGCATAAAAATAGTTATGATTTTTAATCTTTTATTGTGTAAATAAGGAGTATGGCATTTATTGATTCCAACATATTAAAATATTCTTGCATCCCAGGAATAAATCAAGCTTGATCATAATAAATG... | GGCATCCTTATCTTATAATAAATCTCAGAAAAAAGATTCCAACATTTCACCACTGACTATAGTGTTAGCTAATGGCTTATCTTATAGCTAATAAGGAATGTGTCTCTTTATTCTGAGGTATATTCTTTATATACCTAATTTGTTATAAATTGTATTAGAGATGGATTTTAAATTTTGTCAAAATAATTTTAGGCATGCATAAAAATAGTTATGATTTTTAATCTTTTATTGTGTAAATAAGGAGTATGGCATTTATTGATTCCAACATATTAAAATATTCTTGCATCCCAGGAATAAATCAAGCTTGATCATAATAAATG... |
Task1_train_39168 | Here is a genetic alteration on Chromosome 9. Based on the data, is it a benign variant or a cause of disease? | Benign | GAACCCTCTCCCTTGGCACGGGTGTGCTTCTCTCCAGCCCTCCTCCAAGCAGACATCCCAACCAGGGGCAGGCTAATTCAGTCTCCTGTTCCTTTTGACCTTCACCAGCCAGACTCCCTCATGCATATTTCTGATAACTGTGACTCGTTAGATACATTTTAAATTATTATCTTAATATGTAATATTCACACAATTTAATATAAAAATTTTTAGAGGAGCTATAAAATCTCTCCCACCCTAATCTCCTTCTTCAGTCTTCCTTCTTCTCCTAAATACAGGTAATCATTGTAATTTATTTCTTATTCTTTATTTATACACAG... | GAACCCTCTCCCTTGGCACGGGTGTGCTTCTCTCCAGCCCTCCTCCAAGCAGACATCCCAACCAGGGGCAGGCTAATTCAGTCTCCTGTTCCTTTTGACCTTCACCAGCCAGACTCCCTCATGCATATTTCTGATAACTGTGACTCGTTAGATACATTTTAAATTATTATCTTAATATGTAATATTCACACAATTTAATATAAAAATTTTTAGAGGAGCTATAAAATCTCTCCCACCCTAATCTCCTTCTTCAGTCTTCCTTCTTCTCCTAAATACAGGTAATCATTGTAATTTATTTCTTATTCTTTATTTATACACAG... |
Task1_train_39169 | Located on Chromosome 9, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | CTTATAACTACCTTTTGAATTATTTATATTTGCATAAATGTATTTACTGAGTAATATACATGAGTATGCTATATGTATATTTACAACATGTAAATATGAATTTGCATACATATATGAATGATTGTTTTCATAAATGTATATGCGGGTAACTTTTCATGCAATTTCAGTCTCCTCTGTCTGCATTCTCTCCTAGCTCTGTGATTCTAATGGCGTGGGAAAGATAATCTCTCATTTCTTTATCAAATAGAACAGTGAGGAGAAATCAATACCAAATGGAATACCTAATATTTTATATCCCAGCAGTCTTCTGAACATTGTTT... | CTTATAACTACCTTTTGAATTATTTATATTTGCATAAATGTATTTACTGAGTAATATACATGAGTATGCTATATGTATATTTACAACATGTAAATATGAATTTGCATACATATATGAATGATTGTTTTCATAAATGTATATGCGGGTAACTTTTCATGCAATTTCAGTCTCCTCTGTCTGCATTCTCTCCTAGCTCTGTGATTCTAATGGCGTGGGAAAGATAATCTCTCATTTCTTTATCAAATAGAACAGTGAGGAGAAATCAATACCAAATGGAATACCTAATATTTTATATCCCAGCAGTCTTCTGAACATTGTTT... |
Task1_train_39170 | This mutation occurs on Chromosome 9. Does this change lead to a known medical condition, or is it benign? | Benign | GTACCCGCCGCCACCGCTCTCCCACACCTCCCTGGTCCAGCAGCTAGTCCACTGCCCGCCTGGCTGCTCCAGGCGCGCCGACCGCTCAAGCGCTCCAGGTCCACCCGGCGGAGGGCAGAGAAAGCGCGACCGCGCGGCCCGCAGGGTTGCAAGAAGAAAACGAGTGTTATATAATGAGTCTCAGTGGTTGCTCACAATGCCAGGCGCGAAGGCGTGAAGATGTGGCCTTTCCCTTCCCGCATCCCCAGGCATCTTTTGCACCTGGTGCGGAGTGAGCCAGCCAGCTTGCGATAACCAAAGGGCGCCTCAGGCTCTGGCGC... | GTACCCGCCGCCACCGCTCTCCCACACCTCCCTGGTCCAGCAGCTAGTCCACTGCCCGCCTGGCTGCTCCAGGCGCGCCGACCGCTCAAGCGCTCCAGGTCCACCCGGCGGAGGGCAGAGAAAGCGCGACCGCGCGGCCCGCAGGGTTGCAAGAAGAAAACGAGTGTTATATAATGAGTCTCAGTGGTTGCTCACAATGCCAGGCGCGAAGGCGTGAAGATGTGGCCTTTCCCTTCCCGCATCCCCAGGCATCTTTTGCACCTGGTGCGGAGTGAGCCAGCCAGCTTGCGATAACCAAAGGGCGCCTCAGGCTCTGGCGC... |
Task1_train_39171 | This mutation is located on Chromosome 9. Is it associated with a disease or is it a benign polymorphism? | Benign | CAGAGGACAGGATAAAAGCACTCAGAAAAAATGCCAGGAGAAGGCGTTTATCACATAATATCGCTGATAAGAGTCTCTCGAAAATTTTTCTCTCTATTCATTCTTACCAAATATAGAAAGTGAACAAAACAATATTAGTATTAGAAAAAACATCCAAAAATAATGACCTTTCTGAATGAAGACTGCTTTTTTCATGGTTACTCTTTTTGGGGTACAGTTCTATGTTGATTTATCCAATTTATCAAATAGCCATTCAGCAAATATTTATTGAGTGTCTGTTATGTCACAGGCACTCTTTTCGGTCCTCAAAATACATCCGT... | CAGAGGACAGGATAAAAGCACTCAGAAAAAATGCCAGGAGAAGGCGTTTATCACATAATATCGCTGATAAGAGTCTCTCGAAAATTTTTCTCTCTATTCATTCTTACCAAATATAGAAAGTGAACAAAACAATATTAGTATTAGAAAAAACATCCAAAAATAATGACCTTTCTGAATGAAGACTGCTTTTTTCATGGTTACTCTTTTTGGGGTACAGTTCTATGTTGATTTATCCAATTTATCAAATAGCCATTCAGCAAATATTTATTGAGTGTCTGTTATGTCACAGGCACTCTTTTCGGTCCTCAAAATACATCCGT... |
Task1_train_39172 | A variant on Chromosome 9 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | AGTTTGATATCAACATTACCTTAGCTAGTGCTGCTTTATCTTTCATATTCTAGAAATTATTGTACATGCGGATTTCTATTTTTTTTGGTCCAAAAATGGCACCAACAAAAGGTGAAGCATTCCAAACCTACTACTTCAGCTCACTGTAAGGTTTGTCTGTAAGATGAGATCTTTTTCATTGCTCTTCCAAATAAGGTAGGTGGCCTGGTTGCTAGCCAAATGGTCAAAATCGAAGCAGAATCTTAGGGCATTTGTACTAACATAAGCTCTGCTACCTCAGGTCATCTGAAAGAGGTGAAGATGGAGGGAGCACGTCTAGG... | AGTTTGATATCAACATTACCTTAGCTAGTGCTGCTTTATCTTTCATATTCTAGAAATTATTGTACATGCGGATTTCTATTTTTTTTGGTCCAAAAATGGCACCAACAAAAGGTGAAGCATTCCAAACCTACTACTTCAGCTCACTGTAAGGTTTGTCTGTAAGATGAGATCTTTTTCATTGCTCTTCCAAATAAGGTAGGTGGCCTGGTTGCTAGCCAAATGGTCAAAATCGAAGCAGAATCTTAGGGCATTTGTACTAACATAAGCTCTGCTACCTCAGGTCATCTGAAAGAGGTGAAGATGGAGGGAGCACGTCTAGG... |
Task1_train_39173 | Here is a variant on Chromosome 9. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GCTTGGATTTGTTTGTCACAATGGGTGGGTCTCAGTCTCCCATCCCTGAGGCCACTGCAATGCGACAGTGGGACACGTCTCCCCCTGGGTGGGGTGACTGAAGACCTCTTCTTGAAGGAGAATGGGAATCCCCGACAAGCCCCCAGAATTGTTAGAAAGAAAGCTTGAAGTCGTAAAGAAAGACGAGTACTCAAACAAAGGATTTCTCAGCAAAGCAAATTTACTTTTGCGCAGTAGGGTGCTTCTTACAGGGCTGCTTGTCATGAGAGCACACTGAAGAAAGTAGAGTAGAAGCTTTTATTCCTAATGTGACTCCTGCC... | GCTTGGATTTGTTTGTCACAATGGGTGGGTCTCAGTCTCCCATCCCTGAGGCCACTGCAATGCGACAGTGGGACACGTCTCCCCCTGGGTGGGGTGACTGAAGACCTCTTCTTGAAGGAGAATGGGAATCCCCGACAAGCCCCCAGAATTGTTAGAAAGAAAGCTTGAAGTCGTAAAGAAAGACGAGTACTCAAACAAAGGATTTCTCAGCAAAGCAAATTTACTTTTGCGCAGTAGGGTGCTTCTTACAGGGCTGCTTGTCATGAGAGCACACTGAAGAAAGTAGAGTAGAAGCTTTTATTCCTAATGTGACTCCTGCC... |
Task1_train_39174 | A mutation on Chromosome 9 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TGGGGTGACTGAAGACCTCTTCTTGAAGGAGAATGGGAATCCCCGACAAGCCCCCAGAATTGTTAGAAAGAAAGCTTGAAGTCGTAAAGAAAGACGAGTACTCAAACAAAGGATTTCTCAGCAAAGCAAATTTACTTTTGCGCAGTAGGGTGCTTCTTACAGGGCTGCTTGTCATGAGAGCACACTGAAGAAAGTAGAGTAGAAGCTTTTATTCCTAATGTGACTCCTGCCCTCGTGCCCTTTCCCCATTGGCTGGGGTCGGACTGCACAATCTAAACTAGACCCAATTGGCTAAACATTTAAACTTTCTTAGATAAGGT... | TGGGGTGACTGAAGACCTCTTCTTGAAGGAGAATGGGAATCCCCGACAAGCCCCCAGAATTGTTAGAAAGAAAGCTTGAAGTCGTAAAGAAAGACGAGTACTCAAACAAAGGATTTCTCAGCAAAGCAAATTTACTTTTGCGCAGTAGGGTGCTTCTTACAGGGCTGCTTGTCATGAGAGCACACTGAAGAAAGTAGAGTAGAAGCTTTTATTCCTAATGTGACTCCTGCCCTCGTGCCCTTTCCCCATTGGCTGGGGTCGGACTGCACAATCTAAACTAGACCCAATTGGCTAAACATTTAAACTTTCTTAGATAAGGT... |
Task1_train_39175 | Consider this mutation on Chromosome 9. Is this a benign change or a disease-causing variant? | Benign | AGAACATCTTTATATCTACTATTTTTGGTTTTAACCTGGGCTTTTAACTAATTTGAATTTTGGTGTTTCATCCCCAATCTAGTGAAAGACACATTATTCATTAGGAAGCTATTTACATTATTTCATTAGCATTGATATTTAATAGTTATATTAGCAATCTACGTCATATATAGATTGTATGTGTGTCTTTATATATAACCTATCTAAAGACTAAATACCAACTAACGCTGGAAATAACGTAATTGTGGCAGTGGGAGTAATGCCTACAAAGATAATAATAGATGTGATGTAGTTAACTTATTTGTGTTTTGTCAGTTGTT... | AGAACATCTTTATATCTACTATTTTTGGTTTTAACCTGGGCTTTTAACTAATTTGAATTTTGGTGTTTCATCCCCAATCTAGTGAAAGACACATTATTCATTAGGAAGCTATTTACATTATTTCATTAGCATTGATATTTAATAGTTATATTAGCAATCTACGTCATATATAGATTGTATGTGTGTCTTTATATATAACCTATCTAAAGACTAAATACCAACTAACGCTGGAAATAACGTAATTGTGGCAGTGGGAGTAATGCCTACAAAGATAATAATAGATGTGATGTAGTTAACTTATTTGTGTTTTGTCAGTTGTT... |
Task1_train_39176 | This variant lies on Chromosome 9. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GTCTCGATCTCCTGACCTCGTGATCTGCCCGCCTCGGCCTCCTAAAGTGCTGGGATTACAGGCATGAGCCACCATGCCCAGCCTGTTTACTTACTTTTATGACACCATCATCAGTGGTTTTACTGCCAAGTTATAACAGGAGCAAAGTACTCAAAGCATCAAAAAGACCTTACACCTGGACATCATATGGCCTTTAGAAAGTCAGTTACTTTTCTTATGCTGTAATTTCTCCTCTGTAAAATGGAATACTTTATAACATTAGTTCTCATCTTCCTACATTGAAAGAAGAAACACTGTTGGTAGTCAGTAATCAAATTTAG... | GTCTCGATCTCCTGACCTCGTGATCTGCCCGCCTCGGCCTCCTAAAGTGCTGGGATTACAGGCATGAGCCACCATGCCCAGCCTGTTTACTTACTTTTATGACACCATCATCAGTGGTTTTACTGCCAAGTTATAACAGGAGCAAAGTACTCAAAGCATCAAAAAGACCTTACACCTGGACATCATATGGCCTTTAGAAAGTCAGTTACTTTTCTTATGCTGTAATTTCTCCTCTGTAAAATGGAATACTTTATAACATTAGTTCTCATCTTCCTACATTGAAAGAAGAAACACTGTTGGTAGTCAGTAATCAAATTTAG... |
Task1_train_39177 | This variant is located on Chromosome 9. Evaluate its biological effect and specify any disease association. | Benign | GGGGCCGGGTGCGGTGGCTCATGCCTATAGTCCCAACACTTTGGGAGGCCGAGGCAGGTGGGCCACAAGGTCAGGAGATTGAGACCACCCTGGCTAACACGGTGAAACCCCATCTCTACTAAAAAATACAAAAAAAACATAGCCGGGCGTGGTGGCGGGTGCCTGCAATCCCACCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAAACCGGGAGGTGGAGCTCTCAGTGAGCCGAGATGGCACCACTGCACTCCAGCCTGGGCGACAGAGCAAGACTCCATCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGCT... | GGGGCCGGGTGCGGTGGCTCATGCCTATAGTCCCAACACTTTGGGAGGCCGAGGCAGGTGGGCCACAAGGTCAGGAGATTGAGACCACCCTGGCTAACACGGTGAAACCCCATCTCTACTAAAAAATACAAAAAAAACATAGCCGGGCGTGGTGGCGGGTGCCTGCAATCCCACCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAAACCGGGAGGTGGAGCTCTCAGTGAGCCGAGATGGCACCACTGCACTCCAGCCTGGGCGACAGAGCAAGACTCCATCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGCT... |
Task1_train_39178 | Given this context: Chromosome 9 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CTTAATATTGGCATGATCTGCCTCCAGTTAGGGGATACTGCTTCTTACTGGCTTTATTATCCTGACCTTGGACAACTTCCTAAGTCGTCACTTAGTCAATAGAATTTACTTTAGGCCTATTATGTTTCAGCCCCTGTTCTAGGCACTGGGAATAGAGCAGTGAATAATACAGGGGGAAAAAGACTCACCATGGAGCTTACATTCCCACAGGGAGATAAACAGTGAGCAAATAAATAAGTAGAATGTACAGTTCACGAAAATGCTGAGTGTCTTGGAGAAAATTAAAGCAGAAATGGGGGTAGAGAATGCTGGGGCAGGGC... | CTTAATATTGGCATGATCTGCCTCCAGTTAGGGGATACTGCTTCTTACTGGCTTTATTATCCTGACCTTGGACAACTTCCTAAGTCGTCACTTAGTCAATAGAATTTACTTTAGGCCTATTATGTTTCAGCCCCTGTTCTAGGCACTGGGAATAGAGCAGTGAATAATACAGGGGGAAAAAGACTCACCATGGAGCTTACATTCCCACAGGGAGATAAACAGTGAGCAAATAAATAAGTAGAATGTACAGTTCACGAAAATGCTGAGTGTCTTGGAGAAAATTAAAGCAGAAATGGGGGTAGAGAATGCTGGGGCAGGGC... |
Task1_train_39179 | This variant is located on Chromosome 9. Evaluate its biological effect and specify any disease association. | Benign | TTAATGAGTAGGTGATACAGAATGCAAACACAGAATATGCAAATAATGATCAACTGAATATGGTATATATTTCACATATACAATGCATATATTTCTGTGTGATACATGCATTACCTTTATACATGTGTACATCCATATATGCACATGCATTTATACACACACGCATAGAAATACTATGTACATCATGCTATACATGCATGCTTACATATTTATGAGACACACTTTTATGCATGCATATATTTTGGTATACACTTTGCATTTATATATGCATCTGTGTGCTTTTGCATGCACTGCTCCAAATACAAAGATGAATGATATTG... | TTAATGAGTAGGTGATACAGAATGCAAACACAGAATATGCAAATAATGATCAACTGAATATGGTATATATTTCACATATACAATGCATATATTTCTGTGTGATACATGCATTACCTTTATACATGTGTACATCCATATATGCACATGCATTTATACACACACGCATAGAAATACTATGTACATCATGCTATACATGCATGCTTACATATTTATGAGACACACTTTTATGCATGCATATATTTTGGTATACACTTTGCATTTATATATGCATCTGTGTGCTTTTGCATGCACTGCTCCAAATACAAAGATGAATGATATTG... |
Task1_train_39180 | Chromosome 9 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TAAAAAATTAGGTTTGCTGAAATTGAAAGATACACATACTTATCTCTGAACTCTTTCTAACTAATGGTCAGTGAAGAAAAGTGCAAAATCCTTTAGTTTATTAGCTAATGCTTGGAAATGTAACTGTTCATTAATCCTTAATTAACTCAAGTAGCACTGAAGGAAAGGGTCAGAAACATTACTGAATAAAGTATAATAATCAATGACCACTTAATCCCAATAGCTCCCTAGAAGGGACAGATTTAGAAGGAAAGCGAAGACAATGAAATCAAGATGAATAAACAAATAACATTTCTTTGGAACTACTACCAAAAGTACAT... | TAAAAAATTAGGTTTGCTGAAATTGAAAGATACACATACTTATCTCTGAACTCTTTCTAACTAATGGTCAGTGAAGAAAAGTGCAAAATCCTTTAGTTTATTAGCTAATGCTTGGAAATGTAACTGTTCATTAATCCTTAATTAACTCAAGTAGCACTGAAGGAAAGGGTCAGAAACATTACTGAATAAAGTATAATAATCAATGACCACTTAATCCCAATAGCTCCCTAGAAGGGACAGATTTAGAAGGAAAGCGAAGACAATGAAATCAAGATGAATAAACAAATAACATTTCTTTGGAACTACTACCAAAAGTACAT... |
Task1_train_39181 | Given a variant located on Chromosome 9, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GGCTAATATTTTGTATCTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAGGTGGCCCACCCATCTCAGCCTCCCAAAGTGCTGGCACTACAGGTGTGAGCCACCATGCCTGGCCAATTGTTAAATTTTATTACTTTTTACAATTATCTACGCTTTTGAGGTTAGTTACACCTATTGTTATCTATATGGTAGAAATACTATAGAATGATGTGCTGCTGCTCATCTCTTTTTAACACTAGTTCAATGACATCATGTTGGTAGCCTGGAATTCACTACAGTGGGAGCAGTTATACCA... | GGCTAATATTTTGTATCTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAGGTGGCCCACCCATCTCAGCCTCCCAAAGTGCTGGCACTACAGGTGTGAGCCACCATGCCTGGCCAATTGTTAAATTTTATTACTTTTTACAATTATCTACGCTTTTGAGGTTAGTTACACCTATTGTTATCTATATGGTAGAAATACTATAGAATGATGTGCTGCTGCTCATCTCTTTTTAACACTAGTTCAATGACATCATGTTGGTAGCCTGGAATTCACTACAGTGGGAGCAGTTATACCA... |
Task1_train_39182 | This mutation occurs on Chromosome 9. Does this change lead to a known medical condition, or is it benign? | Benign | CATCCCAGCTTTTTTCCATCAAAGCACTGCTGCACTTTATTATTTACTATTTTGTTACCTGCATTCACATAGACACACTAATCACTATTAGGGCAGGGACAGTTTCTACTGTGCTCATCATTGCTTCCTCAACTTTCAATGACACTATTAGGTAATAGGTGCTGAGTAAATTACCTCCAATGCTAACATAATACTGACACGAGTTGCTTATTTTATTCCATCAAAGTGTATCAAATCAATATATGAGTGCATGAAAAAATGGAATTCACACCAGTTGTTAGTGTTTCTTCCAAGTACTTCTTCAGGTGCCAAGCTACACT... | CATCCCAGCTTTTTTCCATCAAAGCACTGCTGCACTTTATTATTTACTATTTTGTTACCTGCATTCACATAGACACACTAATCACTATTAGGGCAGGGACAGTTTCTACTGTGCTCATCATTGCTTCCTCAACTTTCAATGACACTATTAGGTAATAGGTGCTGAGTAAATTACCTCCAATGCTAACATAATACTGACACGAGTTGCTTATTTTATTCCATCAAAGTGTATCAAATCAATATATGAGTGCATGAAAAAATGGAATTCACACCAGTTGTTAGTGTTTCTTCCAAGTACTTCTTCAGGTGCCAAGCTACACT... |
Task1_train_39183 | Here is a mutation located on Chromosome 9. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TACAGACAGGCTCAGGGATTTAAGGGACCTAGGCAAGGTCACATATCCTGTAAGTGGTGACGCCACGATTCAGTCTCATTGCTTTTTTGCTTTTCCCTGAGACCAAGCTCTTTCCAGTACACGGCCAGGCTCGCGCCCCTCGGGAGCGCTTGTGGGAAGCGCAACCCTCGCCTGCCCGCACCAATCCACAGGTGCGCGCAGGAGCCGCTCGGGGGCCCTGGCCCTGGCCCGCCGAGGCCCGGACAGCCCCGCAGGCCATGACCGCAACCCTCGGGTCCCGAGGCGCCGCTCCAGGCGGGAGCGCCAACTCCCACGGCCCT... | TACAGACAGGCTCAGGGATTTAAGGGACCTAGGCAAGGTCACATATCCTGTAAGTGGTGACGCCACGATTCAGTCTCATTGCTTTTTTGCTTTTCCCTGAGACCAAGCTCTTTCCAGTACACGGCCAGGCTCGCGCCCCTCGGGAGCGCTTGTGGGAAGCGCAACCCTCGCCTGCCCGCACCAATCCACAGGTGCGCGCAGGAGCCGCTCGGGGGCCCTGGCCCTGGCCCGCCGAGGCCCGGACAGCCCCGCAGGCCATGACCGCAACCCTCGGGTCCCGAGGCGCCGCTCCAGGCGGGAGCGCCAACTCCCACGGCCCT... |
Task1_train_39184 | This variant is found on Chromosome 9. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TGTTGACATTGTGCGCACCACATCAATCACTTCCCAGCGGGACAACTTTTTAATCTCTTCCTCAGGCACACCAAATTTACGTAGAAGTTGCTTGGCATTTTTCAGGGAAAGGCGACGAAGGTCTGCATCTGTTCCTGTCACTGTCTTCTTCACTGCCTGTGGCTCTTTATCATCCTTCTGCTGTGTTGGTTTATTTGGAATCTTCACATAGGAGAATCCTTCACCACACCCTGTGGGATCTGCCACCCCAGTCACCTCTAGGAGACACTTGCCCTTCATGGCAGCAATGAAGGCCCTTGTGGTGTTCCAAGGAGCAGCGT... | TGTTGACATTGTGCGCACCACATCAATCACTTCCCAGCGGGACAACTTTTTAATCTCTTCCTCAGGCACACCAAATTTACGTAGAAGTTGCTTGGCATTTTTCAGGGAAAGGCGACGAAGGTCTGCATCTGTTCCTGTCACTGTCTTCTTCACTGCCTGTGGCTCTTTATCATCCTTCTGCTGTGTTGGTTTATTTGGAATCTTCACATAGGAGAATCCTTCACCACACCCTGTGGGATCTGCCACCCCAGTCACCTCTAGGAGACACTTGCCCTTCATGGCAGCAATGAAGGCCCTTGTGGTGTTCCAAGGAGCAGCGT... |
Task1_train_39185 | A genomic change on Chromosome 9 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GGTATGCGCCACCACGCCTGGCTAATTTTTTGTATTTTTGGTAGAGATGGGTGTCACCATGTTGACCAGGGCTGGTCTCGAACTCCTGACCTCAAGTGAATGCACCCGCCTCAGCCTCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCATGGTGCCTGGCCCCAAGATGACCTTTAAAGTCCAATTCCCCTTTTATAAGATGGCGTTTTTGCTTTAGGACAGGAAGTCATCATTAAATATTTTCTCTACCTGCCTAAGCAATGGAAAGATAGCTGCCACCTGCCTCAGAGGCATCCCTGGGACTGTGCAGTTTCCTAA... | GGTATGCGCCACCACGCCTGGCTAATTTTTTGTATTTTTGGTAGAGATGGGTGTCACCATGTTGACCAGGGCTGGTCTCGAACTCCTGACCTCAAGTGAATGCACCCGCCTCAGCCTCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCATGGTGCCTGGCCCCAAGATGACCTTTAAAGTCCAATTCCCCTTTTATAAGATGGCGTTTTTGCTTTAGGACAGGAAGTCATCATTAAATATTTTCTCTACCTGCCTAAGCAATGGAAAGATAGCTGCCACCTGCCTCAGAGGCATCCCTGGGACTGTGCAGTTTCCTAA... |
Task1_train_39186 | This alteration occurs on Chromosome 9. Is it associated with a disease or is it a benign variant? | Benign | CTTTTTTTGTTTTCTTCCACTGCCTTTAGGTATAGAGTGCGGATATTGATTTGAGATTTTTTCTTAAAATGTAGTTGTTTATATCCATACATTTTCCTTTGAACTCTACTTTCACTGCATTCAATAAGTTTTGGTATGTTTTGTTTTTATTTTAATTTGTCTCAAGATATTTTATAATTTTGCTTGTAATTTATTTTTTCACTCACTGGTAGTTGAAGACTGTATTGTTTAATTTCCACATTTTCATGAATTTTCCAGTTTTCACTTATTTATCTGTTGTTTCTTCCATTGTGGTTGTAAATTATATTTTGTATGATTTC... | CTTTTTTTGTTTTCTTCCACTGCCTTTAGGTATAGAGTGCGGATATTGATTTGAGATTTTTTCTTAAAATGTAGTTGTTTATATCCATACATTTTCCTTTGAACTCTACTTTCACTGCATTCAATAAGTTTTGGTATGTTTTGTTTTTATTTTAATTTGTCTCAAGATATTTTATAATTTTGCTTGTAATTTATTTTTTCACTCACTGGTAGTTGAAGACTGTATTGTTTAATTTCCACATTTTCATGAATTTTCCAGTTTTCACTTATTTATCTGTTGTTTCTTCCATTGTGGTTGTAAATTATATTTTGTATGATTTC... |
Task1_train_39187 | Given this context: Chromosome 9 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TTTTAATTTATTTGACGAATTGGATGTATTTATCTGGTAATTGATGTAATTCAGCAATATGTAATTGTATCTTCCCTTTTGGTGCCACGAAATGCTAGGCAATGCCACCTTAGGGGCTTTGGGTGAGTTACTTAATATTTCTTGGTTTTACTTCCATTATCAAGTAGATAATGGGGCTAGAGTGGACAGCTATACTGTGTATCTTCCAGCTACAAACTTCTGTGGTGATTGAATGTACATTTGAGGAACATCTCATTTTCCAGGATTCCACACTAGAAACTCAGCAGTTTCACTCGGCTCCTTGTGTTGTGGCAAACTTT... | TTTTAATTTATTTGACGAATTGGATGTATTTATCTGGTAATTGATGTAATTCAGCAATATGTAATTGTATCTTCCCTTTTGGTGCCACGAAATGCTAGGCAATGCCACCTTAGGGGCTTTGGGTGAGTTACTTAATATTTCTTGGTTTTACTTCCATTATCAAGTAGATAATGGGGCTAGAGTGGACAGCTATACTGTGTATCTTCCAGCTACAAACTTCTGTGGTGATTGAATGTACATTTGAGGAACATCTCATTTTCCAGGATTCCACACTAGAAACTCAGCAGTTTCACTCGGCTCCTTGTGTTGTGGCAAACTTT... |
Task1_train_39188 | A mutation on Chromosome 9 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GCCCTTAACATAATATCCTCCAGACTGATCCACGTGGCTACAAGTAAGAAGATTTCATTTTTTTATATGGTGAGTATTCCATTGTGTATGTGTACCACAATTTTTTTGTCCATTCATTTGTTGATGGACATGTAGGTTGATTTTATACATTAGCTGTTGTGAATAGTGCTACAGTAAACATGTGAGGAAAAGTATCCTTGTGATCTATTGTTTTCTTTTCTATTGCCTGAATACCCAGTAGTGGGGTTGCTGGATCCCTCAGCAGTTCCATTGTTCATTTTTTGAGAAAACTTCATATTGTTTTCTATAGTAGCTGCACT... | GCCCTTAACATAATATCCTCCAGACTGATCCACGTGGCTACAAGTAAGAAGATTTCATTTTTTTATATGGTGAGTATTCCATTGTGTATGTGTACCACAATTTTTTTGTCCATTCATTTGTTGATGGACATGTAGGTTGATTTTATACATTAGCTGTTGTGAATAGTGCTACAGTAAACATGTGAGGAAAAGTATCCTTGTGATCTATTGTTTTCTTTTCTATTGCCTGAATACCCAGTAGTGGGGTTGCTGGATCCCTCAGCAGTTCCATTGTTCATTTTTTGAGAAAACTTCATATTGTTTTCTATAGTAGCTGCACT... |
Task1_train_39189 | A variant found on Chromosome 9 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | TATACAGTAAAAGGGGGAATTTGATGATTAAGACCAGTTGGCATAAGAGAAAACTGTGATTTAGAAATTATATGATACTTTTGAATTGGTCTTAAGCTACGTTGTTCATTGTTCACTTTTTAAAATTATAAATGGATTCTATTACTTTTTATAGGACCAGATTACATTAATACTAACATAATTATGATTCCAAATTTTTATAAATCAGACAATTCTGAATTCAGTTATTAGTTTTGTTGATATTGCTGATAAATATTTTAAGCTTCAGCCTCTTTTTAACATATTCAAAATTGCTCTTTGAATCACTGATTCAAAATGAA... | TATACAGTAAAAGGGGGAATTTGATGATTAAGACCAGTTGGCATAAGAGAAAACTGTGATTTAGAAATTATATGATACTTTTGAATTGGTCTTAAGCTACGTTGTTCATTGTTCACTTTTTAAAATTATAAATGGATTCTATTACTTTTTATAGGACCAGATTACATTAATACTAACATAATTATGATTCCAAATTTTTATAAATCAGACAATTCTGAATTCAGTTATTAGTTTTGTTGATATTGCTGATAAATATTTTAAGCTTCAGCCTCTTTTTAACATATTCAAAATTGCTCTTTGAATCACTGATTCAAAATGAA... |
Task1_train_39190 | A change on Chromosome 9 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GAGGGACAGAGTGGGCCAGGGTTGAAAAACTGCTTCTTGGGTCCTATGCTCACTACCTGTGTGATGGGTTCAATTGTACTCCAAACCTCAGCATTCCTCAATATACTTTTGGAAGAAACTTACACAGGTACCACTTTAATTTAGAATACAAACTAGAAAAAAAAAAAGAAAACTTTACTATACATATTTTTTTCAGTAAGTAAAGAATATAAATTTCTTTTTAAGAAAAAATTTATTGAAGTAAAAAATGGATTAAACTTTTATAAAGGACAGACTTTTGCTAAGAATTTCAAAGCAATGCATTCATTGCAAAATATGAC... | GAGGGACAGAGTGGGCCAGGGTTGAAAAACTGCTTCTTGGGTCCTATGCTCACTACCTGTGTGATGGGTTCAATTGTACTCCAAACCTCAGCATTCCTCAATATACTTTTGGAAGAAACTTACACAGGTACCACTTTAATTTAGAATACAAACTAGAAAAAAAAAAAGAAAACTTTACTATACATATTTTTTTCAGTAAGTAAAGAATATAAATTTCTTTTTAAGAAAAAATTTATTGAAGTAAAAAATGGATTAAACTTTTATAAAGGACAGACTTTTGCTAAGAATTTCAAAGCAATGCATTCATTGCAAAATATGAC... |
Task1_train_39191 | Given this context: Chromosome 9 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GTAAGTAATATGTTAATCTCATGATAATGTCTCTTGTTTAACTTAAACATTATTATTATTTTTTTTTTTACTTATTTTAGATGGAGCTGGACTGTGCAGAACAAATAATTACAGAAACAAAGAAAAGTATGTTGCCAAAATGTATTAATTAAATTTAGGTTTATTTTAGTAATAAAGTGTAAATAGCAAATGGCATTCCTTTTCATTGTTGGGTTAGTAGATACTACATTCAGTATCTTTTTCTTACACACATCTAATGAAAGATGTGAAAACAAAAACTTTCACAGTGAAGAGTATACTTATGCATCATTAATTCATCA... | GTAAGTAATATGTTAATCTCATGATAATGTCTCTTGTTTAACTTAAACATTATTATTATTTTTTTTTTTACTTATTTTAGATGGAGCTGGACTGTGCAGAACAAATAATTACAGAAACAAAGAAAAGTATGTTGCCAAAATGTATTAATTAAATTTAGGTTTATTTTAGTAATAAAGTGTAAATAGCAAATGGCATTCCTTTTCATTGTTGGGTTAGTAGATACTACATTCAGTATCTTTTTCTTACACACATCTAATGAAAGATGTGAAAACAAAAACTTTCACAGTGAAGAGTATACTTATGCATCATTAATTCATCA... |
Task1_train_39192 | A mutation found on Chromosome 9 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CACAGGCGAGCTCTTCCCATCATGCGCTCACTAGTCCCCAACAGAAGAACCACTGTCGCATCCACTGAGGTACCAAGAAACTAGCAAAGGGCCTTCTAGCTGTCTGGGGACAGTCCTCATGTGGTCCCTGGCTCAGCCTCAAGGGTTCTTGATTAGTCTCTCTGCAGCCTCTGTGCTGTGTCTCTAGATCGGGGCTCTGTGGGAAGGGCCCTGGGAGACCCAGCAGCACAGGGTGTCTTGTCTGCCAAATGTCCCTCCCTTCCTCCCACTCTGACACTCAGGAATAGGGAAGATGGCATGTCCAGGCAGTGCCAGGCCAC... | CACAGGCGAGCTCTTCCCATCATGCGCTCACTAGTCCCCAACAGAAGAACCACTGTCGCATCCACTGAGGTACCAAGAAACTAGCAAAGGGCCTTCTAGCTGTCTGGGGACAGTCCTCATGTGGTCCCTGGCTCAGCCTCAAGGGTTCTTGATTAGTCTCTCTGCAGCCTCTGTGCTGTGTCTCTAGATCGGGGCTCTGTGGGAAGGGCCCTGGGAGACCCAGCAGCACAGGGTGTCTTGTCTGCCAAATGTCCCTCCCTTCCTCCCACTCTGACACTCAGGAATAGGGAAGATGGCATGTCCAGGCAGTGCCAGGCCAC... |
Task1_train_39193 | This sequence variant lies on Chromosome 9. Is it clinically significant, and what condition might it cause if any? | Benign | TACCTGACAATTAGTGTTTCTCAAAATAAATAGGAAGATTTTCTTCCGATCTGAAGGTCTTCCAGCCACTCCCTCCCAGACATATCATAATATTGGGCCAGAGGTCACCCATAGCAAGCTGTCCTTACTTACTCTTTGCAGAAAAAGTACAGTTACAGTATGAAGTGGCCTCATTTTAATGAGGCCCAACATACCCAAGAAATAAAAATGCAGCCACAGGAGCATACAGATGCCCTTCAATAGATATGTCAATATTAACATAATGCAATAGCTATATTTGTTATAAAATGATTTCACTATTGCACAAACATAATATGATG... | TACCTGACAATTAGTGTTTCTCAAAATAAATAGGAAGATTTTCTTCCGATCTGAAGGTCTTCCAGCCACTCCCTCCCAGACATATCATAATATTGGGCCAGAGGTCACCCATAGCAAGCTGTCCTTACTTACTCTTTGCAGAAAAAGTACAGTTACAGTATGAAGTGGCCTCATTTTAATGAGGCCCAACATACCCAAGAAATAAAAATGCAGCCACAGGAGCATACAGATGCCCTTCAATAGATATGTCAATATTAACATAATGCAATAGCTATATTTGTTATAAAATGATTTCACTATTGCACAAACATAATATGATG... |
Task1_train_39194 | A sequence alteration has been identified on Chromosome 9. Is it disease-inducing or harmless? | Benign | GGTCACCCATAGCAAGCTGTCCTTACTTACTCTTTGCAGAAAAAGTACAGTTACAGTATGAAGTGGCCTCATTTTAATGAGGCCCAACATACCCAAGAAATAAAAATGCAGCCACAGGAGCATACAGATGCCCTTCAATAGATATGTCAATATTAACATAATGCAATAGCTATATTTGTTATAAAATGATTTCACTATTGCACAAACATAATATGATGGGCGAAGTCTTAATCTTATCTTTTCTAGCTACCTATGCCAGAGAAGTAGAACTAAATATTAAATGAAAGCACAATTGGGAGGCTGTTATAAAAATGAAAACA... | GGTCACCCATAGCAAGCTGTCCTTACTTACTCTTTGCAGAAAAAGTACAGTTACAGTATGAAGTGGCCTCATTTTAATGAGGCCCAACATACCCAAGAAATAAAAATGCAGCCACAGGAGCATACAGATGCCCTTCAATAGATATGTCAATATTAACATAATGCAATAGCTATATTTGTTATAAAATGATTTCACTATTGCACAAACATAATATGATGGGCGAAGTCTTAATCTTATCTTTTCTAGCTACCTATGCCAGAGAAGTAGAACTAAATATTAAATGAAAGCACAATTGGGAGGCTGTTATAAAAATGAAAACA... |
Task1_train_39195 | This variant lies on Chromosome 9. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AGAAAAAGTACAGTTACAGTATGAAGTGGCCTCATTTTAATGAGGCCCAACATACCCAAGAAATAAAAATGCAGCCACAGGAGCATACAGATGCCCTTCAATAGATATGTCAATATTAACATAATGCAATAGCTATATTTGTTATAAAATGATTTCACTATTGCACAAACATAATATGATGGGCGAAGTCTTAATCTTATCTTTTCTAGCTACCTATGCCAGAGAAGTAGAACTAAATATTAAATGAAAGCACAATTGGGAGGCTGTTATAAAAATGAAAACATAGGGCTTTCAAAACAACTTTCCAGCTCCTTGTAATT... | AGAAAAAGTACAGTTACAGTATGAAGTGGCCTCATTTTAATGAGGCCCAACATACCCAAGAAATAAAAATGCAGCCACAGGAGCATACAGATGCCCTTCAATAGATATGTCAATATTAACATAATGCAATAGCTATATTTGTTATAAAATGATTTCACTATTGCACAAACATAATATGATGGGCGAAGTCTTAATCTTATCTTTTCTAGCTACCTATGCCAGAGAAGTAGAACTAAATATTAAATGAAAGCACAATTGGGAGGCTGTTATAAAAATGAAAACATAGGGCTTTCAAAACAACTTTCCAGCTCCTTGTAATT... |
Task1_train_39196 | A mutation is present on Chromosome 9. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GTTCTTTTAATAGTGTGCACAGGGTTGACGGGAAACACACACACACTGTGCAGAACCATTCCACGAGGCTGTGTGTCCGGAATTGGTTCCCTCCAATGGGTTCCTGGTGCCGCTGACTTCAAGAATGAAGCCGCGGACCCTCGCAGTGTTACACTTCTTAAAGACGGTGTGTCCAGAGTTTGTTCCTTCAGATGTTCAGATGTGTCAGGAGTTTCTTCCTTCTACTGGGTTCGTGGTCTATGCACGACTTCATGAGTGAAGCCGCAGACCTTTGCAGTGAGCGTTACAGCTCTTAAAGGTGGTGCGTCCGGAGTTGTTTG... | GTTCTTTTAATAGTGTGCACAGGGTTGACGGGAAACACACACACACTGTGCAGAACCATTCCACGAGGCTGTGTGTCCGGAATTGGTTCCCTCCAATGGGTTCCTGGTGCCGCTGACTTCAAGAATGAAGCCGCGGACCCTCGCAGTGTTACACTTCTTAAAGACGGTGTGTCCAGAGTTTGTTCCTTCAGATGTTCAGATGTGTCAGGAGTTTCTTCCTTCTACTGGGTTCGTGGTCTATGCACGACTTCATGAGTGAAGCCGCAGACCTTTGCAGTGAGCGTTACAGCTCTTAAAGGTGGTGCGTCCGGAGTTGTTTG... |
Task1_train_39197 | Here’s a variant located on Chromosome 9. What is the predicted biological effect — harmless or disease-causing? | Benign | TCCTTGAGCACCCAGAAAGAGAATTCTGAACTAAATGTATTCTTTCACATGGCTGAGTTAAGGATAGTGTTAATTACTGAAATATATGTAAGGTTTTTTTTTTTTTTTTGGTTGTTTGAAAACTAAGCCCACCTTTGAAGTCCAGAGATGTCCTTTCACTCTAATGTATGCTGAGGTGGCAACTGGTAACTGCTTCTTTGTAGGTAATAGCCATAGCCTTAGTTTCATCCTCCTTTCTCCATGACTAAAACTTGCTCCAACTTCTGCATTTCGTTTTTATGATGTATTAATGAGGAGCAAAGACATAAAGGGGTTTCAGA... | TCCTTGAGCACCCAGAAAGAGAATTCTGAACTAAATGTATTCTTTCACATGGCTGAGTTAAGGATAGTGTTAATTACTGAAATATATGTAAGGTTTTTTTTTTTTTTTTGGTTGTTTGAAAACTAAGCCCACCTTTGAAGTCCAGAGATGTCCTTTCACTCTAATGTATGCTGAGGTGGCAACTGGTAACTGCTTCTTTGTAGGTAATAGCCATAGCCTTAGTTTCATCCTCCTTTCTCCATGACTAAAACTTGCTCCAACTTCTGCATTTCGTTTTTATGATGTATTAATGAGGAGCAAAGACATAAAGGGGTTTCAGA... |
Task1_train_39198 | This is a variant located on Chromosome 9. Is this mutation a likely cause of disease or not? | Benign | TATCAAAATGAAGAAGAGAAGGAGAGGGAGGGAGAAGGGGGGGAGGGGGAGGGGGAGGAGGAAGGGGAGGAGGAAGGGGAGGAGGAAGGGGAGGAGGAAGGGGAGGAGGAAGGGGGGGAGGAGGGGGAGGGGGAGGAGGGGGAGGGGGAGGAGGAGGAGGAGGGGAGGAGGAGGAGGAGGGGAGGAGGAGGAGGATGGGGAGGAGAAGAAGAGGAGAAGGAAGAAGAAGAAAGAGGGAAGGAAGGAAGAAGAAGAAAAAATAAGGTAGGAGGGAGGAGGGTGAGGAGGAGGGGAAAGAGGAGGGGGAGGGAGAGGAGGGA... | TATCAAAATGAAGAAGAGAAGGAGAGGGAGGGAGAAGGGGGGGAGGGGGAGGGGGAGGAGGAAGGGGAGGAGGAAGGGGAGGAGGAAGGGGAGGAGGAAGGGGAGGAGGAAGGGGGGGAGGAGGGGGAGGGGGAGGAGGGGGAGGGGGAGGAGGAGGAGGAGGGGAGGAGGAGGAGGAGGGGAGGAGGAGGAGGATGGGGAGGAGAAGAAGAGGAGAAGGAAGAAGAAGAAAGAGGGAAGGAAGGAAGAAGAAGAAAAAATAAGGTAGGAGGGAGGAGGGTGAGGAGGAGGGGAAAGAGGAGGGGGAGGGAGAGGAGGGA... |
Task1_train_39199 | A genomic change on Chromosome 9 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TAAATGAGTGATTTTAAGAAGCACTTTTAATTAACTATCAAAGTATAGTCAAATCAATCTGCAAGTAAGACAAACTGGATATAGTTTACTTACTTGCATATTGCCTATGAAAAAGGGTTTGCCAATCTAGTCAATAACATGTATATAATGCTTAATTTTGCACCAGGTACTGTGCTTAGCACTTATCTCACTTCACTTAAAATAATAATATAACCAAATTGAGGAGGAGGGAGTATTTAACATTAAAAATTTTATTCAAATGGGTCTTTGTTTTATTGAGACAGAGTCTCGCTCTGTTGCCCAGGCTTGAATGCAGTGGT... | TAAATGAGTGATTTTAAGAAGCACTTTTAATTAACTATCAAAGTATAGTCAAATCAATCTGCAAGTAAGACAAACTGGATATAGTTTACTTACTTGCATATTGCCTATGAAAAAGGGTTTGCCAATCTAGTCAATAACATGTATATAATGCTTAATTTTGCACCAGGTACTGTGCTTAGCACTTATCTCACTTCACTTAAAATAATAATATAACCAAATTGAGGAGGAGGGAGTATTTAACATTAAAAATTTTATTCAAATGGGTCTTTGTTTTATTGAGACAGAGTCTCGCTCTGTTGCCCAGGCTTGAATGCAGTGGT... |
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