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_32900 | A variant found on Chromosome 1 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | TGTATGCCCTTGACCAAAGAGTAATCTTCCAGGCTTTGGGGCAGAAGGCTGTCATGGCATAGAGACGGAGTAGGGGGACACCACCAAAACAAGATCACATTATCATGATCACAAAACATGTACCAGTAAATCCAATGAAAGTATGCTAACAAAAAGTGGACAGGATGAAAGGAGGTTTCTAATCTCTAGGGGAAATATCTAAATAATGTGTAGCTCAGAGAAAAATGAAAAAGGTCATAATAGGCCAGGTGTGGTGGCTCATGCTTGTAACCCCAGCACTTTGGGAGGCCGAGGCAGGTGGATCACGAGGTCAGGAGTTT... | TGTATGCCCTTGACCAAAGAGTAATCTTCCAGGCTTTGGGGCAGAAGGCTGTCATGGCATAGAGACGGAGTAGGGGGACACCACCAAAACAAGATCACATTATCATGATCACAAAACATGTACCAGTAAATCCAATGAAAGTATGCTAACAAAAAGTGGACAGGATGAAAGGAGGTTTCTAATCTCTAGGGGAAATATCTAAATAATGTGTAGCTCAGAGAAAAATGAAAAAGGTCATAATAGGCCAGGTGTGGTGGCTCATGCTTGTAACCCCAGCACTTTGGGAGGCCGAGGCAGGTGGATCACGAGGTCAGGAGTTT... |
Task1_train_32901 | A variant affecting Chromosome 1 has been observed. Determine if it's benign or associated with disease. | Benign | GTGTCTCAGTCTAATTGGACACTGATCCCTGTGCCTGAAGGGTTTTGAGGCAAATTGAAATAATGTATGTAAAAACACCTAACCTGTTCCTGACATACCATAATTAGGTAAACAATAAATGGCTATTAAATATGAATGTTCCTTAGTGCACAAATCATAAGCCTAATATATCATGATGCTATATGGTATTTTACTGTCCCTGTCAGTGTTGATTTCTGTGGAGGGAAACCTCTGACTACTCCAATGTCAGCAGAGAGATTCTGCTCGACCTGTTAGTATCACCCAATTTTTAAAAACTCATACTCTCTAAAGCAGAAAGT... | GTGTCTCAGTCTAATTGGACACTGATCCCTGTGCCTGAAGGGTTTTGAGGCAAATTGAAATAATGTATGTAAAAACACCTAACCTGTTCCTGACATACCATAATTAGGTAAACAATAAATGGCTATTAAATATGAATGTTCCTTAGTGCACAAATCATAAGCCTAATATATCATGATGCTATATGGTATTTTACTGTCCCTGTCAGTGTTGATTTCTGTGGAGGGAAACCTCTGACTACTCCAATGTCAGCAGAGAGATTCTGCTCGACCTGTTAGTATCACCCAATTTTTAAAAACTCATACTCTCTAAAGCAGAAAGT... |
Task1_train_32902 | A sequence alteration has been identified on Chromosome 1. Is it disease-inducing or harmless? | Benign | CTAAAGCTTGAGATGAAAACAATCTGAGGGGCAGACCATAGCTTTGAGAGAGAATTGAATACAAAACCCACACAAGAAAACACATTTGGTCACGTAACGTTTCATAGTATTATGGGGAGGTAAGACGTAACTAGTGAGTTACACTCCAATATCTTTTTTTTTTTTTTGGACCTGGGGTCTTGCTCTGTTGCCCAGGCTGGAGTGCACTGGCACAATCACAGCTCACTGCAACCTCGACCTCCTGGGCTCAAGGGATCCTCCCATCTCAGCCTCCTGAATAGCTGGGATTATAGGCATATGCCTCCACTCCCGGCTAATTT... | CTAAAGCTTGAGATGAAAACAATCTGAGGGGCAGACCATAGCTTTGAGAGAGAATTGAATACAAAACCCACACAAGAAAACACATTTGGTCACGTAACGTTTCATAGTATTATGGGGAGGTAAGACGTAACTAGTGAGTTACACTCCAATATCTTTTTTTTTTTTTTGGACCTGGGGTCTTGCTCTGTTGCCCAGGCTGGAGTGCACTGGCACAATCACAGCTCACTGCAACCTCGACCTCCTGGGCTCAAGGGATCCTCCCATCTCAGCCTCCTGAATAGCTGGGATTATAGGCATATGCCTCCACTCCCGGCTAATTT... |
Task1_train_32903 | This mutation on Chromosome 1 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | AAAAGCTGTGAGCACTAAATGCTTTACCAATGGTGGATTTGTTTCTGTGGGATAGGATACAGGTAAATTAGTGTCTTGTTCAGATAACACAGGTTCTGTAAGAGAATGATTCTATAGTTCTAATAGAAAAAATATATATTACAGCTTAGGGAATATAAAGGCAAAGAAATAACACTGTAAGGTGGGGTTATATGGGACGGACTTTGTAAATCAGGTTTTTGAGCGGTGTTTTTTTCCAGTTTGCTCATGAAGGAGGATTATATTAGATTTATGTAGTGAGGAGGTAGGGAAGAGGTGTTTGAGCAGGAGTAGTAGAGGCC... | AAAAGCTGTGAGCACTAAATGCTTTACCAATGGTGGATTTGTTTCTGTGGGATAGGATACAGGTAAATTAGTGTCTTGTTCAGATAACACAGGTTCTGTAAGAGAATGATTCTATAGTTCTAATAGAAAAAATATATATTACAGCTTAGGGAATATAAAGGCAAAGAAATAACACTGTAAGGTGGGGTTATATGGGACGGACTTTGTAAATCAGGTTTTTGAGCGGTGTTTTTTTCCAGTTTGCTCATGAAGGAGGATTATATTAGATTTATGTAGTGAGGAGGTAGGGAAGAGGTGTTTGAGCAGGAGTAGTAGAGGCC... |
Task1_train_32904 | A genomic change on Chromosome 1 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GTCTTTCCCTCCATTATGCAGAAACAATGTAATTAAAAGCACCTTTCAGATCATAATGTGCAAACAAACATCAGCTAGTATTATTATAGTTAGTGGATTTGAGAAAAAGACTTTCAATTATTGTGCATTAGTTGCTGTAACACTTTTGTACAACCTCCCCCTTTTTTTCCACTAGTAGAAATCAGGATGTGAGTTGCTTTTACCAAAGTATGAATAATGATGACTAGGAGGGCAAGGAAGTATCTACCATATAATTGGAACCCGATAAACACTCACTGATTTGTTGATGAATGAATGAATGAGTTAGTGTGTAAATGACT... | GTCTTTCCCTCCATTATGCAGAAACAATGTAATTAAAAGCACCTTTCAGATCATAATGTGCAAACAAACATCAGCTAGTATTATTATAGTTAGTGGATTTGAGAAAAAGACTTTCAATTATTGTGCATTAGTTGCTGTAACACTTTTGTACAACCTCCCCCTTTTTTTCCACTAGTAGAAATCAGGATGTGAGTTGCTTTTACCAAAGTATGAATAATGATGACTAGGAGGGCAAGGAAGTATCTACCATATAATTGGAACCCGATAAACACTCACTGATTTGTTGATGAATGAATGAATGAGTTAGTGTGTAAATGACT... |
Task1_train_32905 | A mutation on Chromosome 1 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | AGTGAAAGAACCTGGTCTAGAAAGGCTACATAAGGTATGATTCTAATCATATGACATTCTGGAAAAGGTAAAACTATACAGACAATAAAAAGGTCAGTGGTTCCCAGGTGTTTGGTGGGGTAGTGTGTGTGTGGTTCAGGATGGGTGGAATAAGAAGGGTGAATAGGTGAAGAGGGATTTTTAGGTTGGCAAAATTATTCTGTATGATACATGAGACATAGAATGTACAACACCAAGAGTGAACCCTAATGTAAACTATGGGCTTTAGTTAATAATAATGTAAGATTGGTTCATCAGTTGTTACAAATATACAACACTAA... | AGTGAAAGAACCTGGTCTAGAAAGGCTACATAAGGTATGATTCTAATCATATGACATTCTGGAAAAGGTAAAACTATACAGACAATAAAAAGGTCAGTGGTTCCCAGGTGTTTGGTGGGGTAGTGTGTGTGTGGTTCAGGATGGGTGGAATAAGAAGGGTGAATAGGTGAAGAGGGATTTTTAGGTTGGCAAAATTATTCTGTATGATACATGAGACATAGAATGTACAACACCAAGAGTGAACCCTAATGTAAACTATGGGCTTTAGTTAATAATAATGTAAGATTGGTTCATCAGTTGTTACAAATATACAACACTAA... |
Task1_train_32906 | Given a variant located on Chromosome 1, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TGCACTCAGCCAGTTCAATGGCTATATACATTATGCATGCATTTATAATCCCTCTGGCTTGCCAAAAATGATCCAGTTGGCTGGAATGCAGTCATGTTGACTGTTTTTCATTATTGCCCTTCCAGTAAGACGGCTGTGACTATTTTACAAAATATTAAATCACTTTTGCAAATGCGACATAGGCGTAATAGAAGGACAAACCTATATGGGGCTTGTGGTCATATAAAATGTGTGCTTGGGTTTTTGTTAAGAGTTTAGCCTGTAACTTTTTTGGGTTCTAATCTCTTTTGAGCAACATCTGGCTTTACTCCTGAATTAGA... | TGCACTCAGCCAGTTCAATGGCTATATACATTATGCATGCATTTATAATCCCTCTGGCTTGCCAAAAATGATCCAGTTGGCTGGAATGCAGTCATGTTGACTGTTTTTCATTATTGCCCTTCCAGTAAGACGGCTGTGACTATTTTACAAAATATTAAATCACTTTTGCAAATGCGACATAGGCGTAATAGAAGGACAAACCTATATGGGGCTTGTGGTCATATAAAATGTGTGCTTGGGTTTTTGTTAAGAGTTTAGCCTGTAACTTTTTTGGGTTCTAATCTCTTTTGAGCAACATCTGGCTTTACTCCTGAATTAGA... |
Task1_train_32907 | A genomic variant on Chromosome 1 is under review. What is the biological outcome — benign or pathogenic? | Benign | TAGCTAAAGTCCTCTTTTCTTTTTTTCATATTCTAATCCACAGCATGGTGTCAGTTTTACATACTTTCTGCTTGTTTTCTTTATTGCCAAACTCCTTGGCTGACAAGCATTAACCTTGATTGTTTCAACTGACCTCTTAGGCAGTGTGGTTGAAATGAACATCAATGATATCATCCCACAAACAACTGCCTTCATCTCCCCTTTACCAAGAGTATTTTCCCGATTGTATTCCATTCCAATGAGTTTTCATCAATTTATTTAGCACTTACTCATATGGTTGTGACTCAGAGATTTGGGGTTGGTGCTTTGGGAACCCAAAA... | TAGCTAAAGTCCTCTTTTCTTTTTTTCATATTCTAATCCACAGCATGGTGTCAGTTTTACATACTTTCTGCTTGTTTTCTTTATTGCCAAACTCCTTGGCTGACAAGCATTAACCTTGATTGTTTCAACTGACCTCTTAGGCAGTGTGGTTGAAATGAACATCAATGATATCATCCCACAAACAACTGCCTTCATCTCCCCTTTACCAAGAGTATTTTCCCGATTGTATTCCATTCCAATGAGTTTTCATCAATTTATTTAGCACTTACTCATATGGTTGTGACTCAGAGATTTGGGGTTGGTGCTTTGGGAACCCAAAA... |
Task1_train_32908 | This mutation occurs on Chromosome 1. Does this change lead to a known medical condition, or is it benign? | Benign | TTACTTAAAATTACTTAAAGTGGCATAGAGATTCCTTATTTTACCTATTTGAAAAAGACTGGGGCTAGCCAGCTCTAAAGCAAACAGAGGAAGAGAGAAAGAAAGGGGAGATAGGATTCTTTGACTCACATGTCCTTGATCATCCAACTCATTGTTGGTAAGCTTGAGTTTGTCAAAACTGACCACCTGTCTCATCCAGGTGTCTCCAGAAGCTAGAGAATCAGGGTGTATATAAACTCTTGGGGGCACAGGGGAATCAGCATTGCCAGCCACCATCCACTTGGAGCTATGATACACATATCTGAGATAAAGAGGAAGAG... | TTACTTAAAATTACTTAAAGTGGCATAGAGATTCCTTATTTTACCTATTTGAAAAAGACTGGGGCTAGCCAGCTCTAAAGCAAACAGAGGAAGAGAGAAAGAAAGGGGAGATAGGATTCTTTGACTCACATGTCCTTGATCATCCAACTCATTGTTGGTAAGCTTGAGTTTGTCAAAACTGACCACCTGTCTCATCCAGGTGTCTCCAGAAGCTAGAGAATCAGGGTGTATATAAACTCTTGGGGGCACAGGGGAATCAGCATTGCCAGCCACCATCCACTTGGAGCTATGATACACATATCTGAGATAAAGAGGAAGAG... |
Task1_train_32909 | This variant is found on Chromosome 1. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | AGTGCCTTAATTTTTTGGAGGAAAGGTATTGCAAGGGGGTAAAAACCACACAAACAGATAAACAGACAATTGGCTTGATAGATCTACCTTTAGTTTTGTCATTTTCCAGTATTCACAATCCTTTCAAAGTTTCCTTTAAAGGGGAAAAAACAGAGGCTTGTAAGAAATATGCTCAAAGAGGTTCTAGGACTTACAGACATCCCATTCCAGTATAAGATACAAAAGGCAAAATGTTTCCTTTACCCATGATCCAGGCTAGCTCCAAGAATCCTAAAAACGATGTTTTAATTTGGAATCTGGGATGGGGCGTTTTGTGGATT... | AGTGCCTTAATTTTTTGGAGGAAAGGTATTGCAAGGGGGTAAAAACCACACAAACAGATAAACAGACAATTGGCTTGATAGATCTACCTTTAGTTTTGTCATTTTCCAGTATTCACAATCCTTTCAAAGTTTCCTTTAAAGGGGAAAAAACAGAGGCTTGTAAGAAATATGCTCAAAGAGGTTCTAGGACTTACAGACATCCCATTCCAGTATAAGATACAAAAGGCAAAATGTTTCCTTTACCCATGATCCAGGCTAGCTCCAAGAATCCTAAAAACGATGTTTTAATTTGGAATCTGGGATGGGGCGTTTTGTGGATT... |
Task1_train_32910 | This variant is found on Chromosome 1. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | AAGCAGAGGAAGGCAGCAGGAAGGGCAGAGGTGGAACTAGAACCAGAGAACATCCCACTCTCAGGCTGTTACCCACATCACCACCAGCAGCCTCTTCCCTGACTCCCCCACTCCAGGACCTTCTTGGAGTTGCCTGACAACGGGAAGAGGTTGGGAGTAGACAAAACATGGCAGAGGCATCAGGAGAGCAAGTGGTCCTGCTTGTACCCCAGGAAGGAATTTCTCCAGCTTCGAATTTTTCACTCTGAATTTTGCTCTCACTGGTCTTTGGTCTTTGTTGCCAATTTCAGTTAAACTGGCTTATTCTTTGGAAAAGAATG... | AAGCAGAGGAAGGCAGCAGGAAGGGCAGAGGTGGAACTAGAACCAGAGAACATCCCACTCTCAGGCTGTTACCCACATCACCACCAGCAGCCTCTTCCCTGACTCCCCCACTCCAGGACCTTCTTGGAGTTGCCTGACAACGGGAAGAGGTTGGGAGTAGACAAAACATGGCAGAGGCATCAGGAGAGCAAGTGGTCCTGCTTGTACCCCAGGAAGGAATTTCTCCAGCTTCGAATTTTTCACTCTGAATTTTGCTCTCACTGGTCTTTGGTCTTTGTTGCCAATTTCAGTTAAACTGGCTTATTCTTTGGAAAAGAATG... |
Task1_train_32911 | Given this variant on Chromosome 1, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | AAGTGCACCCTCATTTAATCTTCATCCCTTAAATGCTTGGCGTTTCCTTTCAAAGTATGGCTTTCCAACTACCTTAAATTCAGACACATTTCCTTAAGGAATCTTCTCAGAAATCTCACCCTCTGATCTCCAGAGTCCAGTCTCTTCAGCACCATAGCACCCCAAACCCCGGCCTGGCCCTCCGCATTTAGTCTACTCTGACTCTTTTTCCAAAGCAACCAATTGCTTTTGAGTCTCCAGCACCATAAAAGAAAAAAAAAAACAACTTCCAGTTTCTACTTACCCATACTTCTAAGTACCCCTGCTGTGCAAGGAGGGTG... | AAGTGCACCCTCATTTAATCTTCATCCCTTAAATGCTTGGCGTTTCCTTTCAAAGTATGGCTTTCCAACTACCTTAAATTCAGACACATTTCCTTAAGGAATCTTCTCAGAAATCTCACCCTCTGATCTCCAGAGTCCAGTCTCTTCAGCACCATAGCACCCCAAACCCCGGCCTGGCCCTCCGCATTTAGTCTACTCTGACTCTTTTTCCAAAGCAACCAATTGCTTTTGAGTCTCCAGCACCATAAAAGAAAAAAAAAAACAACTTCCAGTTTCTACTTACCCATACTTCTAAGTACCCCTGCTGTGCAAGGAGGGTG... |
Task1_train_32912 | This mutation is located on Chromosome 1. Is it associated with a disease or is it a benign polymorphism? | Benign | ATAAAAGAAAAAAAAAAACAACTTCCAGTTTCTACTTACCCATACTTCTAAGTACCCCTGCTGTGCAAGGAGGGTGCTAAGAGTAACCAGTTTTAATTACTACTTCAACAGCTCCCAAAAGGAGGGGATATGAAATGACAGGGGAAGTGTTAGAGGCATCTGTTTGCTAAAACCATTATAACTCCCAAGCTTAGAAAATACTTCACAATGTTGGTCATTTCCCCCTTGAAGGTAAACTAACTCCAAATTTTCTCTGCCACAAGATTAATTTTTGAACACATGAGGCTGTCTTTCCAGAAACTCAAATTGCACAGAGACAT... | ATAAAAGAAAAAAAAAAACAACTTCCAGTTTCTACTTACCCATACTTCTAAGTACCCCTGCTGTGCAAGGAGGGTGCTAAGAGTAACCAGTTTTAATTACTACTTCAACAGCTCCCAAAAGGAGGGGATATGAAATGACAGGGGAAGTGTTAGAGGCATCTGTTTGCTAAAACCATTATAACTCCCAAGCTTAGAAAATACTTCACAATGTTGGTCATTTCCCCCTTGAAGGTAAACTAACTCCAAATTTTCTCTGCCACAAGATTAATTTTTGAACACATGAGGCTGTCTTTCCAGAAACTCAAATTGCACAGAGACAT... |
Task1_train_32913 | Located on Chromosome 1, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TATGTTGGCACCAGCCTGTAGTCTCAGCTACTGAGAAGGTTGAGCTGGAAGGATTGCTTGAACCCTGGGAAGTCAAGGCTGCAGTGAGCTGTGATCATGCCAGTACACTCCAGCCTGGGTGACAGAGCGAGGCCTTGTCAAAAAAAAAAAAAAAAAGCCAGGTTGGGTAACTTGATGAAGATATGTAGGCATTGGACTGAGCCCTGAATTCGAGAGACTCTGACCTTGGTAAGATCAATGGTAGGAGCAGCAGGGAATTTGTGCTTTCTGGAGGCAGGTAGATCCTGAAATAGGAGAAAGAAAAGGGCTGAACCACACAC... | TATGTTGGCACCAGCCTGTAGTCTCAGCTACTGAGAAGGTTGAGCTGGAAGGATTGCTTGAACCCTGGGAAGTCAAGGCTGCAGTGAGCTGTGATCATGCCAGTACACTCCAGCCTGGGTGACAGAGCGAGGCCTTGTCAAAAAAAAAAAAAAAAAGCCAGGTTGGGTAACTTGATGAAGATATGTAGGCATTGGACTGAGCCCTGAATTCGAGAGACTCTGACCTTGGTAAGATCAATGGTAGGAGCAGCAGGGAATTTGTGCTTTCTGGAGGCAGGTAGATCCTGAAATAGGAGAAAGAAAAGGGCTGAACCACACAC... |
Task1_train_32914 | A sequence alteration has been identified on Chromosome 1. Is it disease-inducing or harmless? | Benign | TTGGCCCTGTCTCTTCCCTGCTGTGTGACTCTCCCTTCTGAGGCTTGGATTCTTCACTTGTAAAGTGAGAGTTAGGGGCAGATGAGCCAGGAGCGGTGAGGACACTTTGTGCTCTGTAACTTACTAAGGTGGTACCTTGGGCCGTCTGACAGCCCTCGAGAGAGAGTTTGCTCAGCCGTGGAGTGGGAATGAGAACAGTGCCCTCTGACCACCCCTCGGGCTGCTGAGTGGGCTGTGGCCACCTTTGCAGTGGATCCAGTACTGTGCGGATGTGGTTGAGTGACCAAGGAGGGCTCCAGTTTCCTTAACCCTGTAGACGT... | TTGGCCCTGTCTCTTCCCTGCTGTGTGACTCTCCCTTCTGAGGCTTGGATTCTTCACTTGTAAAGTGAGAGTTAGGGGCAGATGAGCCAGGAGCGGTGAGGACACTTTGTGCTCTGTAACTTACTAAGGTGGTACCTTGGGCCGTCTGACAGCCCTCGAGAGAGAGTTTGCTCAGCCGTGGAGTGGGAATGAGAACAGTGCCCTCTGACCACCCCTCGGGCTGCTGAGTGGGCTGTGGCCACCTTTGCAGTGGATCCAGTACTGTGCGGATGTGGTTGAGTGACCAAGGAGGGCTCCAGTTTCCTTAACCCTGTAGACGT... |
Task1_train_32915 | The following genetic variant occurs on Chromosome 1. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CCTAGATTAGCCAAATTCACACAGATAGAAAGCAGGATATTGGTTGGGAGGGGTAAAGGGATGGAAGAATGGAGAATTGTTGTTTAATGGGTATGGGGTTTCAGTTTTGCAAGACGAAAAGAGTTCTGGAGATTATTTGCACAACAATGTAAAATACTTAACACTGCTGAACCACACACATAAAAATGGTTAAGACGGTCAATATTATAGTATGTGTATTTTACCACAATCGAAATTTTTAAAAAATCCTAATGTGTAAATATCCTTATGATTTTTAAATAAATGCTCTCAATTCAGTTTTTTAATTTTCATATAAAGTT... | CCTAGATTAGCCAAATTCACACAGATAGAAAGCAGGATATTGGTTGGGAGGGGTAAAGGGATGGAAGAATGGAGAATTGTTGTTTAATGGGTATGGGGTTTCAGTTTTGCAAGACGAAAAGAGTTCTGGAGATTATTTGCACAACAATGTAAAATACTTAACACTGCTGAACCACACACATAAAAATGGTTAAGACGGTCAATATTATAGTATGTGTATTTTACCACAATCGAAATTTTTAAAAAATCCTAATGTGTAAATATCCTTATGATTTTTAAATAAATGCTCTCAATTCAGTTTTTTAATTTTCATATAAAGTT... |
Task1_train_32916 | This variant lies on Chromosome 1. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AAGATGTGGAGGCAGAGACACGGGGGTCCTTGAAAGGCGTTCCTCACTCCTCCTCTGTGCTACTTAGGAGAGTGGCAAACATAGGGCCAGGTGTCATTCAGCACACACGCACTCACAAAAGCTCTGCCTCTGCAAGCAGACACTGCAAACACAAAATTTTCTTAACAGCCTTGCCCCAGGACACTGCCAGGGCCTGGCATCATCTTGTCATCATTGCACTGTGGTGCAATGCAAGAGTTAGGACAGCTCAGCGTCATTAACCCACCTGAGATCACCCCAAATACTGAAAATGCTTATAGAATCATTTTCTATTCATAAAA... | AAGATGTGGAGGCAGAGACACGGGGGTCCTTGAAAGGCGTTCCTCACTCCTCCTCTGTGCTACTTAGGAGAGTGGCAAACATAGGGCCAGGTGTCATTCAGCACACACGCACTCACAAAAGCTCTGCCTCTGCAAGCAGACACTGCAAACACAAAATTTTCTTAACAGCCTTGCCCCAGGACACTGCCAGGGCCTGGCATCATCTTGTCATCATTGCACTGTGGTGCAATGCAAGAGTTAGGACAGCTCAGCGTCATTAACCCACCTGAGATCACCCCAAATACTGAAAATGCTTATAGAATCATTTTCTATTCATAAAA... |
Task1_train_32917 | Given this context: Chromosome 1 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AACATGCTTGCACCGCCGCTTCTAAATGTTTTAAAAACAGACACCAATGCCCTTCATTGGGGAAATGAAAGACTTTTAAGTAAAACGATTTTGAGTGAAATAATATTTGTTGTTTTAAAAAGTTAATATTAACCACTCTCCATCATATGTTGAAATTATCTTAAGATGTGAAAGTTAAAATTAGAAACCTTGTAAAGGAAAAATAGGAAATAGTTTCATGAACTTGACACAGGAAAATATTTCTTAGACTAGATACTGTAGCACTCACCACAATAAGAAATCAAGCGAATTGCACTTCATTTTTAAAAAGCTTCTCCTTA... | AACATGCTTGCACCGCCGCTTCTAAATGTTTTAAAAACAGACACCAATGCCCTTCATTGGGGAAATGAAAGACTTTTAAGTAAAACGATTTTGAGTGAAATAATATTTGTTGTTTTAAAAAGTTAATATTAACCACTCTCCATCATATGTTGAAATTATCTTAAGATGTGAAAGTTAAAATTAGAAACCTTGTAAAGGAAAAATAGGAAATAGTTTCATGAACTTGACACAGGAAAATATTTCTTAGACTAGATACTGTAGCACTCACCACAATAAGAAATCAAGCGAATTGCACTTCATTTTTAAAAAGCTTCTCCTTA... |
Task1_train_32918 | A variant has been detected on Chromosome 1. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CTGGCGAGGAGCTGCGATCCTTTGGAGGAGAAGGGATGTCAGGTTTTTGGAATTTTCAGCTTTTGTGCTCTGGTTTCTCCCCACCTTTGTGGTTTTATCTACCCTTGGTCTTTGATGATGGCGACCTACAGATGGGGTTTTGGGGTGGATGTCTTTTTTGTTGATGTTGATGCTATTCCTTTCTGTGTGTTAGTTTTCCTTCTAACAGTCAGGTCCCTCAGCTTCAGGTCTGTTGGAGTTTGCTGGAAGTCCACTCCAGACCCTCAAACAGGGATTTCTTGGTGTTGCCTATTCTCTCCCATGTGTTTAAATCCAGGGAG... | CTGGCGAGGAGCTGCGATCCTTTGGAGGAGAAGGGATGTCAGGTTTTTGGAATTTTCAGCTTTTGTGCTCTGGTTTCTCCCCACCTTTGTGGTTTTATCTACCCTTGGTCTTTGATGATGGCGACCTACAGATGGGGTTTTGGGGTGGATGTCTTTTTTGTTGATGTTGATGCTATTCCTTTCTGTGTGTTAGTTTTCCTTCTAACAGTCAGGTCCCTCAGCTTCAGGTCTGTTGGAGTTTGCTGGAAGTCCACTCCAGACCCTCAAACAGGGATTTCTTGGTGTTGCCTATTCTCTCCCATGTGTTTAAATCCAGGGAG... |
Task1_train_32919 | Given a variant located on Chromosome 1, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GTCAGGTTTTTGGAATTTTCAGCTTTTGTGCTCTGGTTTCTCCCCACCTTTGTGGTTTTATCTACCCTTGGTCTTTGATGATGGCGACCTACAGATGGGGTTTTGGGGTGGATGTCTTTTTTGTTGATGTTGATGCTATTCCTTTCTGTGTGTTAGTTTTCCTTCTAACAGTCAGGTCCCTCAGCTTCAGGTCTGTTGGAGTTTGCTGGAAGTCCACTCCAGACCCTCAAACAGGGATTTCTTGGTGTTGCCTATTCTCTCCCATGTGTTTAAATCCAGGGAGAGGTGTATATATGCTTTCTTCCTATTTGTTGGTAGTA... | GTCAGGTTTTTGGAATTTTCAGCTTTTGTGCTCTGGTTTCTCCCCACCTTTGTGGTTTTATCTACCCTTGGTCTTTGATGATGGCGACCTACAGATGGGGTTTTGGGGTGGATGTCTTTTTTGTTGATGTTGATGCTATTCCTTTCTGTGTGTTAGTTTTCCTTCTAACAGTCAGGTCCCTCAGCTTCAGGTCTGTTGGAGTTTGCTGGAAGTCCACTCCAGACCCTCAAACAGGGATTTCTTGGTGTTGCCTATTCTCTCCCATGTGTTTAAATCCAGGGAGAGGTGTATATATGCTTTCTTCCTATTTGTTGGTAGTA... |
Task1_train_32920 | A genetic alteration is present on Chromosome 1. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | AAATGAGGTAATGTACGTAAAGCCCATGGTACACAATGTTTATTAAGTGGTAGATATTAATAATATTGTACCTTTGCACTCCTGTGTTACACACACACATGCACACACACACACACACACACACACATGCACACACACACCCAACTTCTACTCTCTAATTATCCCTCTCAAAGAAATCTTATGGCATCACACTTTCAGCACTCGTGAACTCCCTGTGTGGAAACAGAAAGTTCCCACAGAGTAGAGCAGGCACTAGGTGGCTGGAAGTAGTATGTTTAGTAGGATTGGAAACAAGCTTGAGTTCTAGGCTTCCTGGCTTC... | AAATGAGGTAATGTACGTAAAGCCCATGGTACACAATGTTTATTAAGTGGTAGATATTAATAATATTGTACCTTTGCACTCCTGTGTTACACACACACATGCACACACACACACACACACACACACATGCACACACACACCCAACTTCTACTCTCTAATTATCCCTCTCAAAGAAATCTTATGGCATCACACTTTCAGCACTCGTGAACTCCCTGTGTGGAAACAGAAAGTTCCCACAGAGTAGAGCAGGCACTAGGTGGCTGGAAGTAGTATGTTTAGTAGGATTGGAAACAAGCTTGAGTTCTAGGCTTCCTGGCTTC... |
Task1_train_32921 | Chromosome 1 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AAAGTTATAATTTAAAACTATAAACCAAATATTAGAAGTGTGTCTAGTTCAAAGGGAGGAAAACCATCAAAAACATTTTTAGTGCAATATTTAACATGAGCTATACAACCCTTCCTAAATGCCAAAGGCACACACAGACACACACGCAGACACACAGACACACACACACTCACACTCACGAAGAATACAAATGACTAGAACCAAGAAATGTAAATACATTCTGCTACGTATGGTAAACATAGCCTACAATGTGGAAGAGATTAGAAAATAAACATGGAAATGAAATGTTTTTATTAATTCGCATCAGTACCCACCAAAAC... | AAAGTTATAATTTAAAACTATAAACCAAATATTAGAAGTGTGTCTAGTTCAAAGGGAGGAAAACCATCAAAAACATTTTTAGTGCAATATTTAACATGAGCTATACAACCCTTCCTAAATGCCAAAGGCACACACAGACACACACGCAGACACACAGACACACACACACTCACACTCACGAAGAATACAAATGACTAGAACCAAGAAATGTAAATACATTCTGCTACGTATGGTAAACATAGCCTACAATGTGGAAGAGATTAGAAAATAAACATGGAAATGAAATGTTTTTATTAATTCGCATCAGTACCCACCAAAAC... |
Task1_train_32922 | This alteration occurs on Chromosome 1. Is it associated with a disease or is it a benign variant? | Benign | ATTTAACATGAGCTATACAACCCTTCCTAAATGCCAAAGGCACACACAGACACACACGCAGACACACAGACACACACACACTCACACTCACGAAGAATACAAATGACTAGAACCAAGAAATGTAAATACATTCTGCTACGTATGGTAAACATAGCCTACAATGTGGAAGAGATTAGAAAATAAACATGGAAATGAAATGTTTTTATTAATTCGCATCAGTACCCACCAAAACCAATCAGCATAATCAAATATTATAACACTGAATGTAAAAAACAATCCAGAAGTCCAGAGTGATAGGCAAAAGGTTTTAATTGTATAGA... | ATTTAACATGAGCTATACAACCCTTCCTAAATGCCAAAGGCACACACAGACACACACGCAGACACACAGACACACACACACTCACACTCACGAAGAATACAAATGACTAGAACCAAGAAATGTAAATACATTCTGCTACGTATGGTAAACATAGCCTACAATGTGGAAGAGATTAGAAAATAAACATGGAAATGAAATGTTTTTATTAATTCGCATCAGTACCCACCAAAACCAATCAGCATAATCAAATATTATAACACTGAATGTAAAAAACAATCCAGAAGTCCAGAGTGATAGGCAAAAGGTTTTAATTGTATAGA... |
Task1_train_32923 | Here is a genetic alteration on Chromosome 1. Based on the data, is it a benign variant or a cause of disease? | Benign | GGAGGAGTCTCGCTCTGTTGCCCAGACTGGAGTGCAGTGGTGCGATCTTGGCTCACTGCAACCTCCACCTCCCAGGTTCCAGTGATTCTCCTGCCTCAGCCTCTTGGGAGCTGGGATTACAGGCACATGCCACCACACCCATCTAATTTTTGCCACCATGCCCGGCCTTTTTATATTTTTTAATCATTCTAAATTTGACCATGTATCCAAGTTTTAATAAGAAGTCTGAAATCATTCATTTCACGGTTAAGTCTGGAAGTACTAAATCCATGTGTAAATTGATATTTAGAGTTCATAAAACATGTCTCATAGAAACATGT... | GGAGGAGTCTCGCTCTGTTGCCCAGACTGGAGTGCAGTGGTGCGATCTTGGCTCACTGCAACCTCCACCTCCCAGGTTCCAGTGATTCTCCTGCCTCAGCCTCTTGGGAGCTGGGATTACAGGCACATGCCACCACACCCATCTAATTTTTGCCACCATGCCCGGCCTTTTTATATTTTTTAATCATTCTAAATTTGACCATGTATCCAAGTTTTAATAAGAAGTCTGAAATCATTCATTTCACGGTTAAGTCTGGAAGTACTAAATCCATGTGTAAATTGATATTTAGAGTTCATAAAACATGTCTCATAGAAACATGT... |
Task1_train_32924 | A variant was discovered on Chromosome 1. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | AGGCGTGAGCCACCGCGCCCGGCCTCAAGATTTTTTTCTTTGCATTGGTGCCCTCTTTGCCAATGGACATCGTTTTGTAGAACCCACCCTGAAGTGGAGGCGAGAAGAGCAGCTCTCGCTGGGTCTACTTTTCTTAACTCATTAGTTCTTGAGTGACCTCCTCAGAACTTCAGTAAAACCACAGCAACCCATCATGCTATTAGGCCTCTTCCCAGGCTAATATGCAATTCAAGTCCAAATGCTAATAAACGATGGTGCTGCACTGGTGGCAGCCCTGAGCACACTGCTTCTGAATCTGGGTGCCAAATTTTAGTACCTAA... | AGGCGTGAGCCACCGCGCCCGGCCTCAAGATTTTTTTCTTTGCATTGGTGCCCTCTTTGCCAATGGACATCGTTTTGTAGAACCCACCCTGAAGTGGAGGCGAGAAGAGCAGCTCTCGCTGGGTCTACTTTTCTTAACTCATTAGTTCTTGAGTGACCTCCTCAGAACTTCAGTAAAACCACAGCAACCCATCATGCTATTAGGCCTCTTCCCAGGCTAATATGCAATTCAAGTCCAAATGCTAATAAACGATGGTGCTGCACTGGTGGCAGCCCTGAGCACACTGCTTCTGAATCTGGGTGCCAAATTTTAGTACCTAA... |
Task1_train_32925 | A mutation on Chromosome 1 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CCCCACCCCTCCAGTCAAGACTCAGTAGGAGGAGAGGTCTGGAAGAAAGTTCCCTTCATTCTCACCTGCTGGCAGTCAGCTTCACGAAGACCTGGCTCAGGAGAGAGGAGCAGCTAAACTCAAACTCTAGCAGAAAGGTCACCTAGGGGCAGGGGACACAGGGTAATGGTAGAGTCTTCCTCATGGAACAACTACAGAGGAACAGGAGCCCTTGTGCGCCCCCTTCCCTGAAGTCCCAGGACCCTCAGATCCCAGCCTCTGCCCTCCTAGAGCCCTCTTTTCATCCTAGACCCCAACCCACCTTGGCTCCAGTCTGGAAG... | CCCCACCCCTCCAGTCAAGACTCAGTAGGAGGAGAGGTCTGGAAGAAAGTTCCCTTCATTCTCACCTGCTGGCAGTCAGCTTCACGAAGACCTGGCTCAGGAGAGAGGAGCAGCTAAACTCAAACTCTAGCAGAAAGGTCACCTAGGGGCAGGGGACACAGGGTAATGGTAGAGTCTTCCTCATGGAACAACTACAGAGGAACAGGAGCCCTTGTGCGCCCCCTTCCCTGAAGTCCCAGGACCCTCAGATCCCAGCCTCTGCCCTCCTAGAGCCCTCTTTTCATCCTAGACCCCAACCCACCTTGGCTCCAGTCTGGAAG... |
Task1_train_32926 | Given a variant located on Chromosome 1, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CTTCAGGTGATCTGCCCACCTCAGGATCCCAAAGTGCTGGGATTATAGGCGTGAGCCACCATGCCTGGCTGTATCCAGTTACATTTTTAAGACCAGCCAGGCTTAATATATATTTGGTCTTTAGCTCAATTCAATTTGTTGCATTTTGTCCATTGTACTTCATGTGACACAGAATATATCTTAATTTAAAAAGACATATGTTTGTTGAGCTATCTGTTACGTTGGTATATCTTGGAATTTTAAAAAATATAAACCACAGAAGCCAATTATGGCTGACATTAACAATAAATAGGTTTATCACAGAAATAGTGGGGAACTTG... | CTTCAGGTGATCTGCCCACCTCAGGATCCCAAAGTGCTGGGATTATAGGCGTGAGCCACCATGCCTGGCTGTATCCAGTTACATTTTTAAGACCAGCCAGGCTTAATATATATTTGGTCTTTAGCTCAATTCAATTTGTTGCATTTTGTCCATTGTACTTCATGTGACACAGAATATATCTTAATTTAAAAAGACATATGTTTGTTGAGCTATCTGTTACGTTGGTATATCTTGGAATTTTAAAAAATATAAACCACAGAAGCCAATTATGGCTGACATTAACAATAAATAGGTTTATCACAGAAATAGTGGGGAACTTG... |
Task1_train_32927 | Chromosome 1 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CAAACAAAAGGATAAATAAATCAAAAATAAAAATAAAAAGCAGAGAGTACCTTGGTGAGAGTGAAGTCCTGCTTCCTGGTGCACAGGCTCTTGTTCCTAAAGAGGAAGAAAGATCACACCCGAGAATGTGTGGAAGCAGCAGTGCAGTGTGCAAAGCAGGGACCCTCAGCCTGTCTCCTGGGCTCCATCCAAGTTGCTTGTCTTGTCTGTCCCTCAGTTTCCTCATCTGTTCAGAGGGTACTACAATAATACCTACCTCTGTAAATTGCTGCAATGAATTACATGAGGTATTTCCTGTCAATCTCCTTGAACATTAATTG... | CAAACAAAAGGATAAATAAATCAAAAATAAAAATAAAAAGCAGAGAGTACCTTGGTGAGAGTGAAGTCCTGCTTCCTGGTGCACAGGCTCTTGTTCCTAAAGAGGAAGAAAGATCACACCCGAGAATGTGTGGAAGCAGCAGTGCAGTGTGCAAAGCAGGGACCCTCAGCCTGTCTCCTGGGCTCCATCCAAGTTGCTTGTCTTGTCTGTCCCTCAGTTTCCTCATCTGTTCAGAGGGTACTACAATAATACCTACCTCTGTAAATTGCTGCAATGAATTACATGAGGTATTTCCTGTCAATCTCCTTGAACATTAATTG... |
Task1_train_32928 | A variant has been detected on Chromosome 1. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TACCATACAGGGATAGCTGAGTCTTCATCCTCCTCAGCTCCTATTTGTCCAGTGCACTGAACACCAGCTGCTCTCTTCCTCTCTGGCTCCCATGGCAGCCATGCTCTGTTGCAGAGAGAAGAGGATTGCCTGTTCCCTCTTAAAGGGAACCTCCATTTTGCTTTCTGGGACCACTCTCTTAATGCCGCTTGTCAAAACCAGCTAGGACTCCTTGGGGTCCAATCCCTCTGTGTTTAATCTTCTGTCATCTCTGTCCCACCTGGCTCATCAGGGAGATGCAGAAGGCTGAAGAAAGCAAAGTCCCTGAGGACTCACTGGAG... | TACCATACAGGGATAGCTGAGTCTTCATCCTCCTCAGCTCCTATTTGTCCAGTGCACTGAACACCAGCTGCTCTCTTCCTCTCTGGCTCCCATGGCAGCCATGCTCTGTTGCAGAGAGAAGAGGATTGCCTGTTCCCTCTTAAAGGGAACCTCCATTTTGCTTTCTGGGACCACTCTCTTAATGCCGCTTGTCAAAACCAGCTAGGACTCCTTGGGGTCCAATCCCTCTGTGTTTAATCTTCTGTCATCTCTGTCCCACCTGGCTCATCAGGGAGATGCAGAAGGCTGAAGAAAGCAAAGTCCCTGAGGACTCACTGGAG... |
Task1_train_32929 | A change on Chromosome 1 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CTCTCTCTCTCTTTCTCTCTCAGTGTGTGCGTGTGTCTTTGTGTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTCTGTCTTTCTCTTTCATTCTTTTCCATTTGGCCCTGTTCTGTCCCAACATGAAGGCAATAATTTGTTACCTCATTAATGGATCTATCCTTTTACTTTTTTAACCACTTCCTTATGCTACCCATGAAACCTAGTTGGGGCTCTGTTGTGTGTGATTTCCCCTGGCTTATTCTTTACTTTTTCCTCCTTTTCCAGGCTCAGCAGGGAGCTGCTGGAGGTAGTAGAGCCTGAAGTCTTGCAGGAC... | CTCTCTCTCTCTTTCTCTCTCAGTGTGTGCGTGTGTCTTTGTGTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTCTGTCTTTCTCTTTCATTCTTTTCCATTTGGCCCTGTTCTGTCCCAACATGAAGGCAATAATTTGTTACCTCATTAATGGATCTATCCTTTTACTTTTTTAACCACTTCCTTATGCTACCCATGAAACCTAGTTGGGGCTCTGTTGTGTGTGATTTCCCCTGGCTTATTCTTTACTTTTTCCTCCTTTTCCAGGCTCAGCAGGGAGCTGCTGGAGGTAGTAGAGCCTGAAGTCTTGCAGGAC... |
Task1_train_32930 | This mutation is located on Chromosome 1. Is it associated with a disease or is it a benign polymorphism? | Benign | CTCTCTCTCTCTCTCTCTCTCTCTCTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCTATCTGTCTTTCTCTTTCATTCTTTTCCATTTGGCCCTGTTCTGTCCCAACATGAAGGCAATAATTTGTTACCTCATTAATGGATCTATCCTTTTACTTTTTTTAACCACTTCCTTATGCTACCCATGAAACCTAGTTGGGGCTCTGTTGTGTCTGATTTCCCCTGGCTTATTCTTTACTTTTTCCTCCTTTTCCAGGCTCAGCAGGGAGCTGCTGGAGGTAGTAGAGCCTGAAGTCTTGC... | CTCTCTCTCTCTCTCTCTCTCTCTCTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCTATCTGTCTTTCTCTTTCATTCTTTTCCATTTGGCCCTGTTCTGTCCCAACATGAAGGCAATAATTTGTTACCTCATTAATGGATCTATCCTTTTACTTTTTTTAACCACTTCCTTATGCTACCCATGAAACCTAGTTGGGGCTCTGTTGTGTCTGATTTCCCCTGGCTTATTCTTTACTTTTTCCTCCTTTTCCAGGCTCAGCAGGGAGCTGCTGGAGGTAGTAGAGCCTGAAGTCTTGC... |
Task1_train_32931 | Here is a genetic alteration on Chromosome 1. Based on the data, is it a benign variant or a cause of disease? | Benign | GAGATTGGTAAGAACAAATCTTCTGTCTGTGACATTGTGAATAGAATATTGTTATAATTGTTGTATTTTATTATGAGACGTTAATATTTTACTGTGCCAAATTAAACTTTATCATAGGTATGTATGTATGGGAAAAAACACAGAATACATATAGGGTTTGGTACTATCCATGGTTTCCAATATCCACTGGGGGTTTTGGAACATATTCCCCATGGGTAAGGGGGAACTGCTGTATTTAAGAGAGTGCAAAACTTTTTTGTTGAATCAAATTCACTGGGAGGAATTGGAAGTGACAAGGGAAAGATAGTGAAATAATTTCT... | GAGATTGGTAAGAACAAATCTTCTGTCTGTGACATTGTGAATAGAATATTGTTATAATTGTTGTATTTTATTATGAGACGTTAATATTTTACTGTGCCAAATTAAACTTTATCATAGGTATGTATGTATGGGAAAAAACACAGAATACATATAGGGTTTGGTACTATCCATGGTTTCCAATATCCACTGGGGGTTTTGGAACATATTCCCCATGGGTAAGGGGGAACTGCTGTATTTAAGAGAGTGCAAAACTTTTTTGTTGAATCAAATTCACTGGGAGGAATTGGAAGTGACAAGGGAAAGATAGTGAAATAATTTCT... |
Task1_train_32932 | A variant was discovered on Chromosome 1. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GTTGGTTCCTATTGGTAACAGAATACTTTCTGAAAACATTTCCTCTAGGTAAGTGAAAAGTCTCAGTGTATAAGGCAGGGAAGATGCATTCCATTAAAACCAGAATTGTTTTCTTTTTTCTTTTGAGATGGGTTCTTGCTCTGTTACCCAGGCTGGAGTACAGTGGTATGGGCACAGCTCATTCAGCCTCAACTTCCCATGCTCAGTGATCTACCCACTATAACCTCCCTAGTAGCTGGGAACACAGGTGTGTGCCACCATGCCTGGCTAATTTTTTTTATTATTTGTAGAGACAGAGTTTCACGGTGTTGCCTAGGCTG... | GTTGGTTCCTATTGGTAACAGAATACTTTCTGAAAACATTTCCTCTAGGTAAGTGAAAAGTCTCAGTGTATAAGGCAGGGAAGATGCATTCCATTAAAACCAGAATTGTTTTCTTTTTTCTTTTGAGATGGGTTCTTGCTCTGTTACCCAGGCTGGAGTACAGTGGTATGGGCACAGCTCATTCAGCCTCAACTTCCCATGCTCAGTGATCTACCCACTATAACCTCCCTAGTAGCTGGGAACACAGGTGTGTGCCACCATGCCTGGCTAATTTTTTTTATTATTTGTAGAGACAGAGTTTCACGGTGTTGCCTAGGCTG... |
Task1_train_32933 | This variant lies on Chromosome 1. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AAGTAAGAAATAAGCCTAGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGCGGATCATGAGGTCAGGAGATCGAGACCATCCTGGCTAACATAGTGAAACCCCATCTCTACTAAAAATACAAAAAATTAGCCAGGCGTAGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCTGGGAGGCGGAGCTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAAAAAGAAAAGAAATAA... | AAGTAAGAAATAAGCCTAGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGCGGATCATGAGGTCAGGAGATCGAGACCATCCTGGCTAACATAGTGAAACCCCATCTCTACTAAAAATACAAAAAATTAGCCAGGCGTAGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCTGGGAGGCGGAGCTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAAAAAGAAAAGAAATAA... |
Task1_train_32934 | The following genetic variant occurs on Chromosome 1. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CTGAGCTACTGTACTTCAGAGATTTACACACCTGCCCCCCTGCCTGCCCCCATGGGGTCCCCTCACCTGAGCTCCTCAGCTTGCTTCAGCTGCTCTGCAAGCTTCTCCTCCTTGAACTGTCGCTCATTCCTCAGCATAGATTTTATGAGGTCTTTGCACTCTTCATATTCTGAGAAAAGACAGACACGCCTGCATCAGTGGAAGGCTGGACATGCTGCTGTGGTCATTGCCTACAGGGCAGGAGCCAGGTCCATCCCAAGGACAAAACTCTCCACAGTACCAGGGTCTAGACAGGGATTTCCACGTCTTTACTCTTCAGT... | CTGAGCTACTGTACTTCAGAGATTTACACACCTGCCCCCCTGCCTGCCCCCATGGGGTCCCCTCACCTGAGCTCCTCAGCTTGCTTCAGCTGCTCTGCAAGCTTCTCCTCCTTGAACTGTCGCTCATTCCTCAGCATAGATTTTATGAGGTCTTTGCACTCTTCATATTCTGAGAAAAGACAGACACGCCTGCATCAGTGGAAGGCTGGACATGCTGCTGTGGTCATTGCCTACAGGGCAGGAGCCAGGTCCATCCCAAGGACAAAACTCTCCACAGTACCAGGGTCTAGACAGGGATTTCCACGTCTTTACTCTTCAGT... |
Task1_train_32935 | A mutation found on Chromosome 1 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CTGGGGAGAAGAAAGGCAAACATATGATGGGTTAAAAACTGGTGAAATCAAATAGGCTTAATCAGGACTGAGGGATGTCACTGGTAGCCTTGTTTACTTATTTGAAGATGTTGTTTCCCTGGTTTCACTCTTGTCATCTCCAGTCTTGATCTCCTTTAAGTCAACTTGTCTTAGCTATGCAGTCACCTTGAAACCAAGACATAAACACTTCTACACTTGCTTATACGTTTCTATAAAGCAAGGCTTGGCCCTGAGATTTTTATCCCATGAGTGGCCAATGTTTCTGTGTAGCACAAAAGATTTCATTTTGCTTTTTAAAT... | CTGGGGAGAAGAAAGGCAAACATATGATGGGTTAAAAACTGGTGAAATCAAATAGGCTTAATCAGGACTGAGGGATGTCACTGGTAGCCTTGTTTACTTATTTGAAGATGTTGTTTCCCTGGTTTCACTCTTGTCATCTCCAGTCTTGATCTCCTTTAAGTCAACTTGTCTTAGCTATGCAGTCACCTTGAAACCAAGACATAAACACTTCTACACTTGCTTATACGTTTCTATAAAGCAAGGCTTGGCCCTGAGATTTTTATCCCATGAGTGGCCAATGTTTCTGTGTAGCACAAAAGATTTCATTTTGCTTTTTAAAT... |
Task1_train_32936 | Consider this mutation on Chromosome 1. Is this a benign change or a disease-causing variant? | Benign | AAAACTGGTGAAATCAAATAGGCTTAATCAGGACTGAGGGATGTCACTGGTAGCCTTGTTTACTTATTTGAAGATGTTGTTTCCCTGGTTTCACTCTTGTCATCTCCAGTCTTGATCTCCTTTAAGTCAACTTGTCTTAGCTATGCAGTCACCTTGAAACCAAGACATAAACACTTCTACACTTGCTTATACGTTTCTATAAAGCAAGGCTTGGCCCTGAGATTTTTATCCCATGAGTGGCCAATGTTTCTGTGTAGCACAAAAGATTTCATTTTGCTTTTTAAATTTTTTCCTTTTTTGGTTTTTTGTTTTCTGTTTGA... | AAAACTGGTGAAATCAAATAGGCTTAATCAGGACTGAGGGATGTCACTGGTAGCCTTGTTTACTTATTTGAAGATGTTGTTTCCCTGGTTTCACTCTTGTCATCTCCAGTCTTGATCTCCTTTAAGTCAACTTGTCTTAGCTATGCAGTCACCTTGAAACCAAGACATAAACACTTCTACACTTGCTTATACGTTTCTATAAAGCAAGGCTTGGCCCTGAGATTTTTATCCCATGAGTGGCCAATGTTTCTGTGTAGCACAAAAGATTTCATTTTGCTTTTTAAATTTTTTCCTTTTTTGGTTTTTTGTTTTCTGTTTGA... |
Task1_train_32937 | This is a variant located on Chromosome 1. Is this mutation a likely cause of disease or not? | Benign | TTCCCCTGGCCCAGCTTCGTTCTTACTTCTCCCCGCCGAGCTGCTGTACTTCAGAGATCTACACACCTACCTGCCTGTCTCCCCCTACGGGGTCCCCTCACCTGAGCTCCTCAGCTTGCTTGAGCTGCTCTGCAAGCTTCTCCTCCTTGAACTGTCGCTCATTCCTCAGCATAAATTTTATGAGGTCTTTACACTCTTCATACTCTGAGAAAAGACAGACACGCCTGCCTCAGTGGAAGGCTGGACATGCTGCTGTGGTCACTGCCTACAGGGCAGGAGCCAGGTCCATCCCAAGGACAAAACTCTCCCCAGTACCAGGG... | TTCCCCTGGCCCAGCTTCGTTCTTACTTCTCCCCGCCGAGCTGCTGTACTTCAGAGATCTACACACCTACCTGCCTGTCTCCCCCTACGGGGTCCCCTCACCTGAGCTCCTCAGCTTGCTTGAGCTGCTCTGCAAGCTTCTCCTCCTTGAACTGTCGCTCATTCCTCAGCATAAATTTTATGAGGTCTTTACACTCTTCATACTCTGAGAAAAGACAGACACGCCTGCCTCAGTGGAAGGCTGGACATGCTGCTGTGGTCACTGCCTACAGGGCAGGAGCCAGGTCCATCCCAAGGACAAAACTCTCCCCAGTACCAGGG... |
Task1_train_32938 | This alteration on Chromosome 1 may affect genome function. Does it lead to a disease or is it benign? | Benign | TTAGTAGAGATGGGGTTTCACCATGCTGGCCAGCCTGGTCTCAAACTCCTGACTTCAGGTGATCTGCCCACCTCAGGATCCCAAAGTGCTGGGATTATAGGCGTGAGCCACCATGCCTGGCTGTATCCAGTTACATTTTTAAGACCAGCCAGGCTTAATATATATTTGGTCTTTAGCTCAATTCAATTTGTTGCATTTTGTCCATTGTACTTCATGTGACACAGAATATATCTTAATTTAAAAAGACATATGTTTGTTGAGCTATCTGTTACGTTGGTATATCTTGGAATTTTAAAAAATATAAACCACAGAAGCCAATT... | TTAGTAGAGATGGGGTTTCACCATGCTGGCCAGCCTGGTCTCAAACTCCTGACTTCAGGTGATCTGCCCACCTCAGGATCCCAAAGTGCTGGGATTATAGGCGTGAGCCACCATGCCTGGCTGTATCCAGTTACATTTTTAAGACCAGCCAGGCTTAATATATATTTGGTCTTTAGCTCAATTCAATTTGTTGCATTTTGTCCATTGTACTTCATGTGACACAGAATATATCTTAATTTAAAAAGACATATGTTTGTTGAGCTATCTGTTACGTTGGTATATCTTGGAATTTTAAAAAATATAAACCACAGAAGCCAATT... |
Task1_train_32939 | With a mutation on Chromosome 1, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TCACAACTGACTTGGAACCAATAAAGGAGGGAGTGCGAATGCCTATCTTCCCTCTCAAGTTTCTCCAGACTTTACTGCAGCAGCATGTGTCGCTCCTGGCCCTGCTGTGCCATCCCTCTGCCTCCTCACCACATCTCTCACTCATAGACTCAGGGCTTCCCTCTGGTCAGTACTCCCATGACTCCATGCCGAGTGGCACTAGCAAATGCCCCCCAGCACTTTCCCAGCCCTAGCCAGGGGGCGCTCACAGGTGGGCATCATTTCTCGTGTGGCTGGGAGGCAGCTGACCTTGGTGTTAGTCTACTTGATCAGATCAATGT... | TCACAACTGACTTGGAACCAATAAAGGAGGGAGTGCGAATGCCTATCTTCCCTCTCAAGTTTCTCCAGACTTTACTGCAGCAGCATGTGTCGCTCCTGGCCCTGCTGTGCCATCCCTCTGCCTCCTCACCACATCTCTCACTCATAGACTCAGGGCTTCCCTCTGGTCAGTACTCCCATGACTCCATGCCGAGTGGCACTAGCAAATGCCCCCCAGCACTTTCCCAGCCCTAGCCAGGGGGCGCTCACAGGTGGGCATCATTTCTCGTGTGGCTGGGAGGCAGCTGACCTTGGTGTTAGTCTACTTGATCAGATCAATGT... |
Task1_train_32940 | A variant has been detected on Chromosome 1. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TAAATGCTTTAGAATTCTCATGCTAAGCAAGTAGGGTTAATTTCTGCTGGTGGTTTCTACTCTGTGGTGCTCTTTTGTTGTTTCAGTAACCAGAACACATGATGTTTTAAAGAAGGCAAGGACTAACTTAGAGGTAAGGAAACTACTGCACCAGTCAGAGGCACCAAGCCTGTCCCCCACCCATCACCATCCGTTAGCAGATCTTGTAGGTGACCCTTGGCCTGCTTTGGCCTTCCAGGAGAAGACTTGGGGTCCACTTGCAAGATCACAGGTCCTCAGTGAGCATCCTGCTAGTTTCTGTCCCCATCACCCTCCCACCC... | TAAATGCTTTAGAATTCTCATGCTAAGCAAGTAGGGTTAATTTCTGCTGGTGGTTTCTACTCTGTGGTGCTCTTTTGTTGTTTCAGTAACCAGAACACATGATGTTTTAAAGAAGGCAAGGACTAACTTAGAGGTAAGGAAACTACTGCACCAGTCAGAGGCACCAAGCCTGTCCCCCACCCATCACCATCCGTTAGCAGATCTTGTAGGTGACCCTTGGCCTGCTTTGGCCTTCCAGGAGAAGACTTGGGGTCCACTTGCAAGATCACAGGTCCTCAGTGAGCATCCTGCTAGTTTCTGTCCCCATCACCCTCCCACCC... |
Task1_train_32941 | Located on Chromosome 1, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TCCCCTCACCTGAGCTCCTCAGCTTGCTTCAGCTGCTCTGCAAGCTTCTCCTCCTTGAACTGTCGCTCATTCCTCAGCATAAATTTTATGAGGTCTTTACACTCTTCATACTCTGAGAAAAGACAGACACGCCTGCCTCAGTGGAAGGCTGGACATGCTGCTGTGGTCACTGCCTACAGGGCAGGAGCCAGGTCCATCCCAAGGACAAAACTCTCCCCAGTACCAGGGTCTAGACAGGGATTTCCACATCTTTACTCTTCAGTCTCCTGACTTTCTGGCATCTGATCCTCCAAAATTTAAAGACGAAGAAAGAGAACCTC... | TCCCCTCACCTGAGCTCCTCAGCTTGCTTCAGCTGCTCTGCAAGCTTCTCCTCCTTGAACTGTCGCTCATTCCTCAGCATAAATTTTATGAGGTCTTTACACTCTTCATACTCTGAGAAAAGACAGACACGCCTGCCTCAGTGGAAGGCTGGACATGCTGCTGTGGTCACTGCCTACAGGGCAGGAGCCAGGTCCATCCCAAGGACAAAACTCTCCCCAGTACCAGGGTCTAGACAGGGATTTCCACATCTTTACTCTTCAGTCTCCTGACTTTCTGGCATCTGATCCTCCAAAATTTAAAGACGAAGAAAGAGAACCTC... |
Task1_train_32942 | Mutation context: Chromosome 1. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | ATACAGGGACAGAAACAGCAAGATATGTTTGGGGGAATCTCAAGTTAGCCAATACTGTTATTGTGTGAAGTTCACAACAGGGGCAGGGAGGACAGGAGATGGGGCCCAATGACGAAAAGGCCTTGTATGTACCATGTTTAGAAGTTTGAATTTTATCCTATAGGAGTCAGGGAGAGGTTCTATGGGTAGGATTTCCCATCCCAACAGGATTGTAAACTCCCACATCCAATTAGTCACACCTCCATTTTTTTTTCTGTTTCTTTAACATTGTCTCAGATTCATTCCTTCTGAAATCTACCTTATTAGTTCAGGTCTTCTTA... | ATACAGGGACAGAAACAGCAAGATATGTTTGGGGGAATCTCAAGTTAGCCAATACTGTTATTGTGTGAAGTTCACAACAGGGGCAGGGAGGACAGGAGATGGGGCCCAATGACGAAAAGGCCTTGTATGTACCATGTTTAGAAGTTTGAATTTTATCCTATAGGAGTCAGGGAGAGGTTCTATGGGTAGGATTTCCCATCCCAACAGGATTGTAAACTCCCACATCCAATTAGTCACACCTCCATTTTTTTTTCTGTTTCTTTAACATTGTCTCAGATTCATTCCTTCTGAAATCTACCTTATTAGTTCAGGTCTTCTTA... |
Task1_train_32943 | Here’s a variant located on Chromosome 1. What is the predicted biological effect — harmless or disease-causing? | Benign | TTCCATTGCTGGCGAGGAGCTGCGATCCTTTGGAGGAGAAGGGATGTCAGGTTTTTGGAATTTTCAGCTTTTGTGCTCTGGTTTCTCCCCACCTTTGTGGTTTTATCTACCCTTGGTCTTTGATGATGGCGACCTACAGATGGGGTTTTGGGGTGGATGTCTTTTTTGTTGATGTTGATGCTATTCCTTTCTGTGTGTTAGTTTTCCTTCTAACAGTCAGGTCCCTCAGCTTCAGGTCTGTTGGAGTTTGCTGGAAGTCCACTCCAGACCCTCAAACAGGGATTTCTTGGTGTTGCCTATTCTCTCCCATGTGTTTAAAT... | TTCCATTGCTGGCGAGGAGCTGCGATCCTTTGGAGGAGAAGGGATGTCAGGTTTTTGGAATTTTCAGCTTTTGTGCTCTGGTTTCTCCCCACCTTTGTGGTTTTATCTACCCTTGGTCTTTGATGATGGCGACCTACAGATGGGGTTTTGGGGTGGATGTCTTTTTTGTTGATGTTGATGCTATTCCTTTCTGTGTGTTAGTTTTCCTTCTAACAGTCAGGTCCCTCAGCTTCAGGTCTGTTGGAGTTTGCTGGAAGTCCACTCCAGACCCTCAAACAGGGATTTCTTGGTGTTGCCTATTCTCTCCCATGTGTTTAAAT... |
Task1_train_32944 | A change on Chromosome 1 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TTATCAAGTTCTTCCTATCTGTTGTCATACGTCTGGGGATATAAAGACATTTGAGTATAGTTCTTGCTTCAAGGAGCTCACAAGGTGGATTTATCAGACAGTGATTTTGTAAACTGCAAATCACCACCTCCCCAAGTATCTCTATTTAACTGAGGCAGAGGGATTGTGAGCTCTAGAACAAAGTCTCCTTGGGGGGGAAAAAAGTTCATCTTCAACCCAAATTCATTTCAAGTATTAAATGGCACAGAGATATCAGTTGTCTCTGGAACTAGGGAGTAAGTCCACTGACAGGGCCCAGCAATTAAGCTCTTCCAAGGAGC... | TTATCAAGTTCTTCCTATCTGTTGTCATACGTCTGGGGATATAAAGACATTTGAGTATAGTTCTTGCTTCAAGGAGCTCACAAGGTGGATTTATCAGACAGTGATTTTGTAAACTGCAAATCACCACCTCCCCAAGTATCTCTATTTAACTGAGGCAGAGGGATTGTGAGCTCTAGAACAAAGTCTCCTTGGGGGGGAAAAAAGTTCATCTTCAACCCAAATTCATTTCAAGTATTAAATGGCACAGAGATATCAGTTGTCTCTGGAACTAGGGAGTAAGTCCACTGACAGGGCCCAGCAATTAAGCTCTTCCAAGGAGC... |
Task1_train_32945 | A change on Chromosome 1 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TGTCTCTGGAACTAGGGAGTAAGTCCACTGACAGGGCCCAGCAATTAAGCTCTTCCAAGGAGCCTGTCCCTGTCTATACACCATATAGCCAGTTAGAGCTACCGCCAGTTCCTTCCTGCTCCCTGAAATGACCAGTGCCTCCCTGAGGACAGGCACATCAGGTCTCAGCCAACCTTCCCTTCCAAACATAACTCAGCTAGACCCCTCTGGTCTCTAAATAGTATCTCTTCTCTTTGTCTTTTTCTGTTTCAGGCCTCCAGTTACCAACTCCTGTCTGGTTTCATGTCCTTTTCTATCTGGCAGTGGGAATAATGTTTTTA... | TGTCTCTGGAACTAGGGAGTAAGTCCACTGACAGGGCCCAGCAATTAAGCTCTTCCAAGGAGCCTGTCCCTGTCTATACACCATATAGCCAGTTAGAGCTACCGCCAGTTCCTTCCTGCTCCCTGAAATGACCAGTGCCTCCCTGAGGACAGGCACATCAGGTCTCAGCCAACCTTCCCTTCCAAACATAACTCAGCTAGACCCCTCTGGTCTCTAAATAGTATCTCTTCTCTTTGTCTTTTTCTGTTTCAGGCCTCCAGTTACCAACTCCTGTCTGGTTTCATGTCCTTTTCTATCTGGCAGTGGGAATAATGTTTTTA... |
Task1_train_32946 | This variant is present on Chromosome 1. Is the change likely to result in a pathogenic outcome? | Benign | ATGGTTGTACAACATTGTAAATATAATAAAACTCACTGAATTGTATACTTCAGTGAAGGGTAAATTTTATGGTATGTACATTATGTCTCAATAAAGCTGTTTAAAGAATAAATTGGGGTCAAGAAGACAGGAAACCAGTGAGTCTGTGGGAGAGGTGGGAGAGGTGGGAGGTGAGTAGAAAACAGTCTCACTGGCCGGGCACGACGGCTTGTGCCTGTAATCCCAGCGCTTTAGGAGGCCTTGGTGGGTGGATCATCTGAGGAGTTTGAGACCAGCCTAGTCTAACACGGGGAACATGGTGAAACCTCGTCTCTACTAAA... | ATGGTTGTACAACATTGTAAATATAATAAAACTCACTGAATTGTATACTTCAGTGAAGGGTAAATTTTATGGTATGTACATTATGTCTCAATAAAGCTGTTTAAAGAATAAATTGGGGTCAAGAAGACAGGAAACCAGTGAGTCTGTGGGAGAGGTGGGAGAGGTGGGAGGTGAGTAGAAAACAGTCTCACTGGCCGGGCACGACGGCTTGTGCCTGTAATCCCAGCGCTTTAGGAGGCCTTGGTGGGTGGATCATCTGAGGAGTTTGAGACCAGCCTAGTCTAACACGGGGAACATGGTGAAACCTCGTCTCTACTAAA... |
Task1_train_32947 | Located on Chromosome 1, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | GGTTGGGGTGCACTGGGGGATCACCTGGTGGCTACGTCGAACCTCTCGTTGACCGTGCTGACCCTCCAGCCTCTGGCTGCCTGCTTCTTCCGCTCAGTCTCCCAGTCTTCCGCTGTCTCCATGAGAGGAATTGGTGGTTTTCTGGAGCCAGAACCCTGGCCTAGAACAGGAGTGAGACATAGAGGAGGAAGGAGAAAATCAGAGACAGCTTCTCAGCTCTTTGTCATCAGCCATCCTCTGCTTTTTCAGACTCTTCCTTACCCTAAAGCACTCTCACTCACCAGCCTTGCTCAGGGTTATCCCCGAATACTGTTGGGCTT... | GGTTGGGGTGCACTGGGGGATCACCTGGTGGCTACGTCGAACCTCTCGTTGACCGTGCTGACCCTCCAGCCTCTGGCTGCCTGCTTCTTCCGCTCAGTCTCCCAGTCTTCCGCTGTCTCCATGAGAGGAATTGGTGGTTTTCTGGAGCCAGAACCCTGGCCTAGAACAGGAGTGAGACATAGAGGAGGAAGGAGAAAATCAGAGACAGCTTCTCAGCTCTTTGTCATCAGCCATCCTCTGCTTTTTCAGACTCTTCCTTACCCTAAAGCACTCTCACTCACCAGCCTTGCTCAGGGTTATCCCCGAATACTGTTGGGCTT... |
Task1_train_32948 | A mutation on Chromosome 1 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | AAACAAATATTAGCAACTTCCAGTCTAAATAAGAGATGTTATTTTTAATAATAAAAAATACTTTAAATTATGAGTTTTTAAAATAAACTTCAATTTAACATTAGGAGAAAATAACTAACCTAAACTCCCAGGGGCTGTAGATAACTTGTTCTAGTCAACTGACATTTCCCATGAGCCTACCATGTACCAGTCAGTGTACTAGATGCTGAGATACAAAGGTGAGTGGCACTCCCCTTAAGGAGCTCACCACTTAGCAGGAAGTGGCCAAATTATTTTACAAGTGTCTGTAGGCAATAGAATTCTGATCACGATTCAGAGGT... | AAACAAATATTAGCAACTTCCAGTCTAAATAAGAGATGTTATTTTTAATAATAAAAAATACTTTAAATTATGAGTTTTTAAAATAAACTTCAATTTAACATTAGGAGAAAATAACTAACCTAAACTCCCAGGGGCTGTAGATAACTTGTTCTAGTCAACTGACATTTCCCATGAGCCTACCATGTACCAGTCAGTGTACTAGATGCTGAGATACAAAGGTGAGTGGCACTCCCCTTAAGGAGCTCACCACTTAGCAGGAAGTGGCCAAATTATTTTACAAGTGTCTGTAGGCAATAGAATTCTGATCACGATTCAGAGGT... |
Task1_train_32949 | Here is a genetic alteration on Chromosome 1. Based on the data, is it a benign variant or a cause of disease? | Benign | TTAGTGGCTTAGGCCACTCTGTATATTAGGAAAGATTTTTTAGCACCAGAGTGACATGATCTGATTTATGTTTTAGGGCAATAATTGGTGTAGGAAAAGAGAGTGGAAATAGGGCAACCTACTTATTCACATTTCAGATGAGTTGTTCTTTAGGATCCCTTCACAACCACTTTCTTGTTCTCAAGTTCAGGTTTAATGCCTCCTGTGAGTTTGTTTTTGTTTTGTTTTTCCTTGAGACAAGAGTCTGTTGCCCAGGCTGGAGTGCAGTGGCACCATCTCGGCTCACTACAGCCTCCACCCCGAGTTCAAGGGATTCTCCT... | TTAGTGGCTTAGGCCACTCTGTATATTAGGAAAGATTTTTTAGCACCAGAGTGACATGATCTGATTTATGTTTTAGGGCAATAATTGGTGTAGGAAAAGAGAGTGGAAATAGGGCAACCTACTTATTCACATTTCAGATGAGTTGTTCTTTAGGATCCCTTCACAACCACTTTCTTGTTCTCAAGTTCAGGTTTAATGCCTCCTGTGAGTTTGTTTTTGTTTTGTTTTTCCTTGAGACAAGAGTCTGTTGCCCAGGCTGGAGTGCAGTGGCACCATCTCGGCTCACTACAGCCTCCACCCCGAGTTCAAGGGATTCTCCT... |
Task1_train_32950 | A mutation on Chromosome 1 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TGAACCCAGGAGGCAGAGGTTGCAGTGAGCCAAGACCATACCACTGCACTCCAGCCTGGGCGACACAGCGAGACTCCATCTCAAAAAAAAAAAGAAAGAAAGTCCAGCAAAGTGTCACAAACAAGAGGAGTCTAAGGAGAAAGAAGACATGACTACTAAATGTTCTGTGGTATCTTGGATGGGATCCTAGGTTAGAAAAGGACATTAGGTAAAAAAAAAAAAAAACCTGAGGAAATCTAAAGTATGGACTTTTGTTAATAATTATGAATATTGATTCATTAATGTGACAAATGTATCATACTGATATAAGATGTTAGTAA... | TGAACCCAGGAGGCAGAGGTTGCAGTGAGCCAAGACCATACCACTGCACTCCAGCCTGGGCGACACAGCGAGACTCCATCTCAAAAAAAAAAAGAAAGAAAGTCCAGCAAAGTGTCACAAACAAGAGGAGTCTAAGGAGAAAGAAGACATGACTACTAAATGTTCTGTGGTATCTTGGATGGGATCCTAGGTTAGAAAAGGACATTAGGTAAAAAAAAAAAAAAACCTGAGGAAATCTAAAGTATGGACTTTTGTTAATAATTATGAATATTGATTCATTAATGTGACAAATGTATCATACTGATATAAGATGTTAGTAA... |
Task1_train_32951 | A variant found on Chromosome 1 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CCAGGGCACTCCTGCAGGAAGCTGCTGAGGATGTCAGCAAATCTGTCCACTTCTCTGTGAAGCCCCATGCCATCATTCTTCCCAGCTCCTGGTCTTTTGTGTCTGCAGATCACCTACAAGTGACCCTTCCCTGTGCCTGTCCCAGTCCCCCAGGCCCTAAATTGAGACCTAAACTAAGGCGGAGCTGAGACTGGCTGAAGGGGAAGCACTCAACCTTCAGGAAGCCTCCTTAACCAAAGGCCTAAAGATGTTTCAAGGGCCTGGAGTAGGAGGGTGGGTGGAGGAGGTGGATTGGGTAGGCTCCAACCAGCTCAAGGTCC... | CCAGGGCACTCCTGCAGGAAGCTGCTGAGGATGTCAGCAAATCTGTCCACTTCTCTGTGAAGCCCCATGCCATCATTCTTCCCAGCTCCTGGTCTTTTGTGTCTGCAGATCACCTACAAGTGACCCTTCCCTGTGCCTGTCCCAGTCCCCCAGGCCCTAAATTGAGACCTAAACTAAGGCGGAGCTGAGACTGGCTGAAGGGGAAGCACTCAACCTTCAGGAAGCCTCCTTAACCAAAGGCCTAAAGATGTTTCAAGGGCCTGGAGTAGGAGGGTGGGTGGAGGAGGTGGATTGGGTAGGCTCCAACCAGCTCAAGGTCC... |
Task1_train_32952 | A change on Chromosome 1 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | AGAGATGGCCATCCCAACATGGCTTTTGCTTACTCCTTCTACCCAGTAGACCCACCTCTTCCATATCAGGAGGAGATAATCATCCATTCCATGCCGAGAGAGGGTGAGTGACAGCTTTGGTCTGTCCATCCTCCTGCCTTAGTGCTCAGGACCCTGGGGAGAGGAGCAGGAAGCCCGAGCCTTGAGAAGCAGGAGGAGGTGGGGGCAGGCTGTGAGCTGACACCTTTCACACCTCGCTTCTCTTTTCCTTTCAGTTATTTTAAAAGGAAGAGCCACAAATTGTTCTTTCTCATTTCCACTATATCCTCCCAACCCTTTCT... | AGAGATGGCCATCCCAACATGGCTTTTGCTTACTCCTTCTACCCAGTAGACCCACCTCTTCCATATCAGGAGGAGATAATCATCCATTCCATGCCGAGAGAGGGTGAGTGACAGCTTTGGTCTGTCCATCCTCCTGCCTTAGTGCTCAGGACCCTGGGGAGAGGAGCAGGAAGCCCGAGCCTTGAGAAGCAGGAGGAGGTGGGGGCAGGCTGTGAGCTGACACCTTTCACACCTCGCTTCTCTTTTCCTTTCAGTTATTTTAAAAGGAAGAGCCACAAATTGTTCTTTCTCATTTCCACTATATCCTCCCAACCCTTTCT... |
Task1_train_32953 | This alteration occurs on Chromosome 1. Is it associated with a disease or is it a benign variant? | Benign | GGCGCATCCTCAGTGGAGCCTTCCTCCTCTACTTTCTAGGCACCTCTGGGAGGGCAGGAGTGGGAGCAGATGACAACCATTTTAGAAGGAGCCCTCTGGCTGGGTGCGGTGGCTCACACCTGTCATCCCAGCACTTTGGGAGGCCAAGGCAGGAGAAGCGCTTGAGGCCTGGAGTTCAAGACCAGCCTGTGCAATTTAGCTGGATCCCATCTCCACCAAAAAATACCAAAATTAGCTGGGTGTGGTGGTGCACGCATGTAGTCCCACCTACTCAGGAGGCTGAGGAAGGAGAGCCTGTGAGTTTGAGGCTGCAATGAGCT... | GGCGCATCCTCAGTGGAGCCTTCCTCCTCTACTTTCTAGGCACCTCTGGGAGGGCAGGAGTGGGAGCAGATGACAACCATTTTAGAAGGAGCCCTCTGGCTGGGTGCGGTGGCTCACACCTGTCATCCCAGCACTTTGGGAGGCCAAGGCAGGAGAAGCGCTTGAGGCCTGGAGTTCAAGACCAGCCTGTGCAATTTAGCTGGATCCCATCTCCACCAAAAAATACCAAAATTAGCTGGGTGTGGTGGTGCACGCATGTAGTCCCACCTACTCAGGAGGCTGAGGAAGGAGAGCCTGTGAGTTTGAGGCTGCAATGAGCT... |
Task1_train_32954 | Here is a variant on Chromosome 1. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GCCATGGAGGGAGGATTGCTTGAGACTAGTAGTTCCAGATTAGCCTGGGCAATATGATGAGACCTCGTCTCTATGAAAAAATTTTAAAAATTAGCCAGGTGTGGTGGCATGTTTCTGTCACCTGAGGCTGAGGTGAGAGGATCGCTTGAGCCCAGAAGTTTGAGGCTGCAGTAGCCGTGATCATCCCACTGCGCTCCAGCCTGGGAGACAGGACGAGACCCTGACTCAAACACAAACAAACAAAAAAACCCAAGCCAGGCGCAATGGCTTACGCCTGTGTTCCCAGCACTTTGGGAGGCTGAGGTGGGCAGATCACTTGG... | GCCATGGAGGGAGGATTGCTTGAGACTAGTAGTTCCAGATTAGCCTGGGCAATATGATGAGACCTCGTCTCTATGAAAAAATTTTAAAAATTAGCCAGGTGTGGTGGCATGTTTCTGTCACCTGAGGCTGAGGTGAGAGGATCGCTTGAGCCCAGAAGTTTGAGGCTGCAGTAGCCGTGATCATCCCACTGCGCTCCAGCCTGGGAGACAGGACGAGACCCTGACTCAAACACAAACAAACAAAAAAACCCAAGCCAGGCGCAATGGCTTACGCCTGTGTTCCCAGCACTTTGGGAGGCTGAGGTGGGCAGATCACTTGG... |
Task1_train_32955 | A sequence alteration has been identified on Chromosome 1. Is it disease-inducing or harmless? | Benign | TAATTTTTATTTTTATTTTTTGTAGAGTCAGGGCCTCACTATATTGCCTAGGTTGGTTTCTAACTCCTGGGCTCAAGCGATCCTTCTGCCTCTGCCTCCCAAAGTGCTGGAATCACAGATGTGAGCCACTGTGCCTGGCCACCATTTACTTCCTAATAAATTTTTACTTTCTTCATTGATCACAACCTGGGGTAGCTGCTCAGAATGCTTTGATTCCTCTCACTTACCCTGACCTCTATGGTGATACATGTGTTTTACCTCTAACTAATTTAGGATTTTTGCAATTTTTTTAAAACAAGCAAACTAAAGGAAAATACAAC... | TAATTTTTATTTTTATTTTTTGTAGAGTCAGGGCCTCACTATATTGCCTAGGTTGGTTTCTAACTCCTGGGCTCAAGCGATCCTTCTGCCTCTGCCTCCCAAAGTGCTGGAATCACAGATGTGAGCCACTGTGCCTGGCCACCATTTACTTCCTAATAAATTTTTACTTTCTTCATTGATCACAACCTGGGGTAGCTGCTCAGAATGCTTTGATTCCTCTCACTTACCCTGACCTCTATGGTGATACATGTGTTTTACCTCTAACTAATTTAGGATTTTTGCAATTTTTTTAAAACAAGCAAACTAAAGGAAAATACAAC... |
Task1_train_32956 | Chromosome 1 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GGAAATGTAAAGTAAAACCACAATGAGATATCACCTCACATCTGTTAGAATGGCTATTATCAAAACGATGAAAGATAAGTGTTGGTGAGGATGTGGAGAAAAGGGAACCCTCATACACTTTTAGTAGGAATGTAAATTAGTACAGCCATTTGGGAAAACAGTATGGAGGTTCCTCAAAAAACTAAAAATATAATTACCATATCATCCAGCAATCTCACTTCTGGGTATATGTCCCAAGGAAGCGCAATCAGTATGTCAATGAGATAGCTGCACTTCCATGTTCATTGTAGCATTATTCACAATAGCCAAGATACGGAATC... | GGAAATGTAAAGTAAAACCACAATGAGATATCACCTCACATCTGTTAGAATGGCTATTATCAAAACGATGAAAGATAAGTGTTGGTGAGGATGTGGAGAAAAGGGAACCCTCATACACTTTTAGTAGGAATGTAAATTAGTACAGCCATTTGGGAAAACAGTATGGAGGTTCCTCAAAAAACTAAAAATATAATTACCATATCATCCAGCAATCTCACTTCTGGGTATATGTCCCAAGGAAGCGCAATCAGTATGTCAATGAGATAGCTGCACTTCCATGTTCATTGTAGCATTATTCACAATAGCCAAGATACGGAATC... |
Task1_train_32957 | This sequence change occurs on Chromosome 1. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CCGGCAACCTGGAGAGGATTGTGATGGCTCTGCTGCAGCCCACAGCCCAGTTTGACGCCCAGGAATTGAGGACAGCTCTGAAGGTAGCAGGAGGGGAGACTTGCTGGGGTGTCTGGGGAAGGGAGAAGGCTGTCAGCCTTGCTTTTGCAAGACGAGAGTCCCCCTCTCGTCGTCCCATATTGTTTCTTAGAAGGAGAAGCAGCCAGCGTCTGCCCCTCTGTCTGCCATCCTAATGACACGGCCAGTCTGAGAGTAGACTCCCAATTTCTTGTAGGCCTCAGATTCTGCTGTGGACGTGGCCATTGAAATTCTTGCCACTC... | CCGGCAACCTGGAGAGGATTGTGATGGCTCTGCTGCAGCCCACAGCCCAGTTTGACGCCCAGGAATTGAGGACAGCTCTGAAGGTAGCAGGAGGGGAGACTTGCTGGGGTGTCTGGGGAAGGGAGAAGGCTGTCAGCCTTGCTTTTGCAAGACGAGAGTCCCCCTCTCGTCGTCCCATATTGTTTCTTAGAAGGAGAAGCAGCCAGCGTCTGCCCCTCTGTCTGCCATCCTAATGACACGGCCAGTCTGAGAGTAGACTCCCAATTTCTTGTAGGCCTCAGATTCTGCTGTGGACGTGGCCATTGAAATTCTTGCCACTC... |
Task1_train_32958 | Here is a variant on Chromosome 1. Please identify whether it is a benign mutation or associated with a disorder. | Benign | AAAAACAGAAACAAAAACAAAAAGTCAGGCTTTGGTTCCCCCTGCAGGCTATATTAGAAATGACAGGTAGCTGGGCGCAGTGGCTCACGCCTGTAATTCCAGCACTTCGGGAGGCCAAGGCAGGCGGATTACTTGAGGTCAGGAATTCAAGACTAGCCTGACCAAAGTGGCGAAACCGTCTCTACTAAAAATACAAAAATTAGCTGGGCGCAGTGGCGCATGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTAGGAGAATCGCTTGAATCCGGGAGGCGGAGGTTGCAGTGAGCTCAGATTGCACCACTGCACTCCAG... | AAAAACAGAAACAAAAACAAAAAGTCAGGCTTTGGTTCCCCCTGCAGGCTATATTAGAAATGACAGGTAGCTGGGCGCAGTGGCTCACGCCTGTAATTCCAGCACTTCGGGAGGCCAAGGCAGGCGGATTACTTGAGGTCAGGAATTCAAGACTAGCCTGACCAAAGTGGCGAAACCGTCTCTACTAAAAATACAAAAATTAGCTGGGCGCAGTGGCGCATGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTAGGAGAATCGCTTGAATCCGGGAGGCGGAGGTTGCAGTGAGCTCAGATTGCACCACTGCACTCCAG... |
Task1_train_32959 | This mutation is located on Chromosome 1. Is it associated with a disease or is it a benign polymorphism? | Benign | CCACCCTCACCTGTGGATCAACAAGCCAGCCATGGTACAGAGGTATGCCTAGCAGGTCAAAGACACTGCACTCGGGTGTATACTCAAAATCAGAGACGCCTGTGAATCGCACATTGACATCCAGACCTGTGGCCAGTTTAGGCAGCACTGTCATTGCATCATCCACATTCTGGGGGTAGAAAAAAAAATGATGGAGATTCTAGCCTTCTCTCCCACCACTCCACTCCCACCTGCAGAAATTAAAAATTAACCTTGCTGCTCTTCTTCCCTGATTCTCTTACAAGCCACTCCATTTCTCCCTTGCCTCAACCCTTCTCTAT... | CCACCCTCACCTGTGGATCAACAAGCCAGCCATGGTACAGAGGTATGCCTAGCAGGTCAAAGACACTGCACTCGGGTGTATACTCAAAATCAGAGACGCCTGTGAATCGCACATTGACATCCAGACCTGTGGCCAGTTTAGGCAGCACTGTCATTGCATCATCCACATTCTGGGGGTAGAAAAAAAAATGATGGAGATTCTAGCCTTCTCTCCCACCACTCCACTCCCACCTGCAGAAATTAAAAATTAACCTTGCTGCTCTTCTTCCCTGATTCTCTTACAAGCCACTCCATTTCTCCCTTGCCTCAACCCTTCTCTAT... |
Task1_train_32960 | The following genetic variant occurs on Chromosome 1. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TTAGGCAGCACTGTCATTGCATCATCCACATTCTGGGGGTAGAAAAAAAAATGATGGAGATTCTAGCCTTCTCTCCCACCACTCCACTCCCACCTGCAGAAATTAAAAATTAACCTTGCTGCTCTTCTTCCCTGATTCTCTTACAAGCCACTCCATTTCTCCCTTGCCTCAACCCTTCTCTATCTTATATAAATGAACATTGTTTTTCTTTGAGAGTCTAAGTCTAATTCTTTCATCCAGGCTGGAGTGCAGTGGTGTGATCCTAGCTCACTGCAGCCTCAAACTCTTGGTTTCAAGTGACCCTCCCACCTCAGCCTCCT... | TTAGGCAGCACTGTCATTGCATCATCCACATTCTGGGGGTAGAAAAAAAAATGATGGAGATTCTAGCCTTCTCTCCCACCACTCCACTCCCACCTGCAGAAATTAAAAATTAACCTTGCTGCTCTTCTTCCCTGATTCTCTTACAAGCCACTCCATTTCTCCCTTGCCTCAACCCTTCTCTATCTTATATAAATGAACATTGTTTTTCTTTGAGAGTCTAAGTCTAATTCTTTCATCCAGGCTGGAGTGCAGTGGTGTGATCCTAGCTCACTGCAGCCTCAAACTCTTGGTTTCAAGTGACCCTCCCACCTCAGCCTCCT... |
Task1_train_32961 | A variant on Chromosome 1 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GTGAATAAACAGTCCGGAGAGACTTCCCCACCACCCAGCTCTTACTGGGTCAAATCTCGGGTTCCTCAAGGAGACAAGACTGTAAGAGAGTTTGCAGAGAAGAGATGAGGGTGGTTTTAGGTAGGAAATGTCAGTATGGTATGGAACTGGGGAACAGGATTCCAGGATAATTCCCTGGTTTAAAAATAAAGGAAGTTTCTGTAATATGTTGTACCTGATAAATCTGCCTGTGTTCTTTTATTTTCTAACCCTCACCCTCCAGAATGGCCATCAGGAAAGCTGAACCAGAACCGAGTTTAGGTCCAGGTTCTCGTTCTGGC... | GTGAATAAACAGTCCGGAGAGACTTCCCCACCACCCAGCTCTTACTGGGTCAAATCTCGGGTTCCTCAAGGAGACAAGACTGTAAGAGAGTTTGCAGAGAAGAGATGAGGGTGGTTTTAGGTAGGAAATGTCAGTATGGTATGGAACTGGGGAACAGGATTCCAGGATAATTCCCTGGTTTAAAAATAAAGGAAGTTTCTGTAATATGTTGTACCTGATAAATCTGCCTGTGTTCTTTTATTTTCTAACCCTCACCCTCCAGAATGGCCATCAGGAAAGCTGAACCAGAACCGAGTTTAGGTCCAGGTTCTCGTTCTGGC... |
Task1_train_32962 | A mutation on Chromosome 1 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GGATGATGAAAGAATATCATAGAGATAGATGGATCACAATCTGGAGTCCAGTTCATTTCAGGGCTGATAGAGAAGAAAGAGTTTCACATGACATGCAGTTTTCTCACTAGCCAGGCATGCTGATGTGTACCCATAGCCCTAGCTACTTGGGAAGCTGGGGTGGGAGTATCACTTGAGCCCAGGAGGTCAAAGCTGCAGTGAGCAAAGGTCGAGCCACTGTACTCCAGCTTGGATAGCAGAGTGAGTCCCTGTCTCTAAAAGAAAACAACAACAACAACAATAATAATAATATAATTTTCTCATTCAGGCAGCTACATGGA... | GGATGATGAAAGAATATCATAGAGATAGATGGATCACAATCTGGAGTCCAGTTCATTTCAGGGCTGATAGAGAAGAAAGAGTTTCACATGACATGCAGTTTTCTCACTAGCCAGGCATGCTGATGTGTACCCATAGCCCTAGCTACTTGGGAAGCTGGGGTGGGAGTATCACTTGAGCCCAGGAGGTCAAAGCTGCAGTGAGCAAAGGTCGAGCCACTGTACTCCAGCTTGGATAGCAGAGTGAGTCCCTGTCTCTAAAAGAAAACAACAACAACAACAATAATAATAATATAATTTTCTCATTCAGGCAGCTACATGGA... |
Task1_train_32963 | With a mutation on Chromosome 1, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TGTCTCATCTGAATATGTGGTTTTCTTTTTCTTTTAGTTTTCCAAATTGAGAGTCTCCTGTGGATATATAGGTGATAATTGTAAGGTATTATATACTTGTGATTTTCTATAATGTTTTTTAGAGTATTTTCTAAAGGTTTAACTGTCTCTGGAGTGTACTTGGGTTATAGGCTTCTGTAATTAGCTAGAAATTAAACAAAATCAATATAATAAGAATGCATTCCTAGACTAATAAATTCCTTGTTTCCTTTTCTCTAATATGCCCTGGTTAATAAGAAATTGTCTAGGCTGAGCGTGGTGGCTCACGCCTGTAATCCCAG... | TGTCTCATCTGAATATGTGGTTTTCTTTTTCTTTTAGTTTTCCAAATTGAGAGTCTCCTGTGGATATATAGGTGATAATTGTAAGGTATTATATACTTGTGATTTTCTATAATGTTTTTTAGAGTATTTTCTAAAGGTTTAACTGTCTCTGGAGTGTACTTGGGTTATAGGCTTCTGTAATTAGCTAGAAATTAAACAAAATCAATATAATAAGAATGCATTCCTAGACTAATAAATTCCTTGTTTCCTTTTCTCTAATATGCCCTGGTTAATAAGAAATTGTCTAGGCTGAGCGTGGTGGCTCACGCCTGTAATCCCAG... |
Task1_train_32964 | This alteration on Chromosome 1 may affect genome function. Does it lead to a disease or is it benign? | Benign | AAGAAGGAAGGAAAGAAAGAAAGAAACTGGCAAACTATTTTCTTTTTTTTTTTTTTTTCAAATGGAGTCTCACTCTGTCACCCAAGCTGGAGTGCAGTGGCACTATCTCAGCTAACAGCAACCTCCGCATACCAGGTTCAAGTGATTGTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCAGGTGCCACCACACCCGGCTGATTTTTGTATTTTTTGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGAGCTCAGGCAGTCTGCCTGCCTCGACCCCCCAAAGTGCTGGGATTACAGGG... | AAGAAGGAAGGAAAGAAAGAAAGAAACTGGCAAACTATTTTCTTTTTTTTTTTTTTTTCAAATGGAGTCTCACTCTGTCACCCAAGCTGGAGTGCAGTGGCACTATCTCAGCTAACAGCAACCTCCGCATACCAGGTTCAAGTGATTGTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCAGGTGCCACCACACCCGGCTGATTTTTGTATTTTTTGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGAGCTCAGGCAGTCTGCCTGCCTCGACCCCCCAAAGTGCTGGGATTACAGGG... |
Task1_train_32965 | A genetic alteration is present on Chromosome 1. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | AAGGAAGGAAAGAAAGAAAGAAACTGGCAAACTATTTTCTTTTTTTTTTTTTTTTCAAATGGAGTCTCACTCTGTCACCCAAGCTGGAGTGCAGTGGCACTATCTCAGCTAACAGCAACCTCCGCATACCAGGTTCAAGTGATTGTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCAGGTGCCACCACACCCGGCTGATTTTTGTATTTTTTGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGAGCTCAGGCAGTCTGCCTGCCTCGACCCCCCAAAGTGCTGGGATTACAGGGCAT... | AAGGAAGGAAAGAAAGAAAGAAACTGGCAAACTATTTTCTTTTTTTTTTTTTTTTCAAATGGAGTCTCACTCTGTCACCCAAGCTGGAGTGCAGTGGCACTATCTCAGCTAACAGCAACCTCCGCATACCAGGTTCAAGTGATTGTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCAGGTGCCACCACACCCGGCTGATTTTTGTATTTTTTGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGAGCTCAGGCAGTCTGCCTGCCTCGACCCCCCAAAGTGCTGGGATTACAGGGCAT... |
Task1_train_32966 | This sequence variant lies on Chromosome 1. Is it clinically significant, and what condition might it cause if any? | Benign | GTCTATATTTAAACCTTAGGATCATTTACCCTTTTTGTTTGTGACCACCTTCAAGGCAAGAACTATATTTGAGTTTTGTCCCTCAGAGGACTGTGAAAGGCTGCAGCCTTGAAACTTTTCCTTGTCCTTCAAAATTTCGGTTTGAAGAGGATAATGAAGTCAAGTGACTGGATTCTCTACTCCTTCCTTGCTTGCTTTCCTCCAGTATCTAGGAAACTAGCACTGGCCCCGAGGCACCTTGGTTTAAGTAAGGCACCCCATACGGGAAAAACTGAGACCTAAAGGACCACTTCAACCTGGTGAAACAAGCGCCAAGCAAA... | GTCTATATTTAAACCTTAGGATCATTTACCCTTTTTGTTTGTGACCACCTTCAAGGCAAGAACTATATTTGAGTTTTGTCCCTCAGAGGACTGTGAAAGGCTGCAGCCTTGAAACTTTTCCTTGTCCTTCAAAATTTCGGTTTGAAGAGGATAATGAAGTCAAGTGACTGGATTCTCTACTCCTTCCTTGCTTGCTTTCCTCCAGTATCTAGGAAACTAGCACTGGCCCCGAGGCACCTTGGTTTAAGTAAGGCACCCCATACGGGAAAAACTGAGACCTAAAGGACCACTTCAACCTGGTGAAACAAGCGCCAAGCAAA... |
Task1_train_32967 | Chromosome 1 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AAGTGATTGGCCTCCCAAAGTGCTGGGATTACAGATGTGAGCCACCACACCCGGCCATTTGTGTCCTCTTTCAAACAGCAAAAGTAAGGCACTGAAGAAACTTGCTTGTACTGCACGCCCCTGATAAAGCTGAACGAGGATCATTTCTTAAGTCTTGGCTTATGGCATTGTCCCTTTGTACATGCAGCCTTTCAGATCTGTGTGGACCCCAGAAGATCCGTGAAGAATATGAATTGATTCCATGCGGACATGAATGAGTCCTTAAACCTAGAACATCATGTACATCATCCTCCTTAATAATAGTATTGATTATTTGGTTC... | AAGTGATTGGCCTCCCAAAGTGCTGGGATTACAGATGTGAGCCACCACACCCGGCCATTTGTGTCCTCTTTCAAACAGCAAAAGTAAGGCACTGAAGAAACTTGCTTGTACTGCACGCCCCTGATAAAGCTGAACGAGGATCATTTCTTAAGTCTTGGCTTATGGCATTGTCCCTTTGTACATGCAGCCTTTCAGATCTGTGTGGACCCCAGAAGATCCGTGAAGAATATGAATTGATTCCATGCGGACATGAATGAGTCCTTAAACCTAGAACATCATGTACATCATCCTCCTTAATAATAGTATTGATTATTTGGTTC... |
Task1_train_32968 | Here is a genetic alteration on Chromosome 1. Based on the data, is it a benign variant or a cause of disease? | Benign | TAAAATCTGCTGTGGTGGAAATAAATGAACACATGAAGTCTCCCTGAAAGAAAATCAGTGTTTCTTGGGAAGAACCAAGATTCCCTGACAGAAGCTACCCTATGTAGAGGACAAAGTAGGTCTTCAATAAATATTAGTTGGTTTACTGCTTTTCCCAAGGATACATCTGGAGGGTCTGCATTCCTTTCTCATTGGTGCCGCCTGACCACAGAACTAGCTTTTTCCGTGACATCTAACCTAAACCCCGCAGTCCTAAGTCCTGACACGTATGACAAGATGCTGCCACCTGGTGGATACAGAATAGATTTAATGAAATGGCT... | TAAAATCTGCTGTGGTGGAAATAAATGAACACATGAAGTCTCCCTGAAAGAAAATCAGTGTTTCTTGGGAAGAACCAAGATTCCCTGACAGAAGCTACCCTATGTAGAGGACAAAGTAGGTCTTCAATAAATATTAGTTGGTTTACTGCTTTTCCCAAGGATACATCTGGAGGGTCTGCATTCCTTTCTCATTGGTGCCGCCTGACCACAGAACTAGCTTTTTCCGTGACATCTAACCTAAACCCCGCAGTCCTAAGTCCTGACACGTATGACAAGATGCTGCCACCTGGTGGATACAGAATAGATTTAATGAAATGGCT... |
Task1_train_32969 | A genomic change on Chromosome 1 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | ACAGGAAAAAGAAAGAAATGACACTGAAGGATCACTTCCGCTTCCGTTGGCGCAAGCGCTTTCATTTTTTCTGCTACCGTGACTAAGATGGAAGCGTTTTTGGGGTCGCGGTCCGGACTTTGGGCGGGGGGTCCGGCCCCAGGACAGTTTTACCGCATTCCGTCCACTCCCGATTCCTTCATGGATCCGGCGTCTGCACTTTACAGAGGTCCAATCACGCGGACCCAGTAAGTTCTCGGCGCTTTCGTTTGCGTAGCGGGAGGGACCGTGGGGCCTGGTGCTGCCGGCTGGTTTTGAGAGCCCGGGAAGGTGAGGCGGGG... | ACAGGAAAAAGAAAGAAATGACACTGAAGGATCACTTCCGCTTCCGTTGGCGCAAGCGCTTTCATTTTTTCTGCTACCGTGACTAAGATGGAAGCGTTTTTGGGGTCGCGGTCCGGACTTTGGGCGGGGGGTCCGGCCCCAGGACAGTTTTACCGCATTCCGTCCACTCCCGATTCCTTCATGGATCCGGCGTCTGCACTTTACAGAGGTCCAATCACGCGGACCCAGTAAGTTCTCGGCGCTTTCGTTTGCGTAGCGGGAGGGACCGTGGGGCCTGGTGCTGCCGGCTGGTTTTGAGAGCCCGGGAAGGTGAGGCGGGG... |
Task1_train_32970 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TCTGATTCAGGGCTTTGCAAGGGGTTAGAAGCTGACTGTAAAAATGGGAAGAGGCAACGGAAGACATTTATTTCTCCTTTGGATTTTGGGGAGAACCAAGCCCTGGTAGGGAAGAGGTAAGGGGGATGATTCACCTCCATATTTCCTAAGCAGGTTGTATAGGGAGCCGGTGGCAGGAGGAAGGCTGTTTTCACAAATGACTTGTAATGTCGTGATTAAAAAAATTCCTATATTCTTCTGCAAATCAAACGTTCTTTCCCAATCCAATCCAGCCTTGGTTTTATTTTAAATTAAATATTAAAATTACACATTTATATTGA... | TCTGATTCAGGGCTTTGCAAGGGGTTAGAAGCTGACTGTAAAAATGGGAAGAGGCAACGGAAGACATTTATTTCTCCTTTGGATTTTGGGGAGAACCAAGCCCTGGTAGGGAAGAGGTAAGGGGGATGATTCACCTCCATATTTCCTAAGCAGGTTGTATAGGGAGCCGGTGGCAGGAGGAAGGCTGTTTTCACAAATGACTTGTAATGTCGTGATTAAAAAAATTCCTATATTCTTCTGCAAATCAAACGTTCTTTCCCAATCCAATCCAGCCTTGGTTTTATTTTAAATTAAATATTAAAATTACACATTTATATTGA... |
Task1_train_32971 | Assess the clinical impact of this variant found on Chromosome 1. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | ATCCACCTGAAAATGAATGTTTTTTTCTACTAATGAAACTCTGAACTTACAGAAAACTATCTACTTTCAGGCCAGGCATGGTGGCTCATGCCTGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGAGGGTGGATCATGAGGTCAGGAGTTTGAGACCATCCTGGTCAATATGGTGAAACCCCATCTCTACTAAAAATATAAAAAATTAGCCGGGTGCTGTGGCACATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCAGGGAGGCGGAGGTGCAGTGAGCTGAGATTATGCCACTGCAC... | ATCCACCTGAAAATGAATGTTTTTTTCTACTAATGAAACTCTGAACTTACAGAAAACTATCTACTTTCAGGCCAGGCATGGTGGCTCATGCCTGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGAGGGTGGATCATGAGGTCAGGAGTTTGAGACCATCCTGGTCAATATGGTGAAACCCCATCTCTACTAAAAATATAAAAAATTAGCCGGGTGCTGTGGCACATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCAGGGAGGCGGAGGTGCAGTGAGCTGAGATTATGCCACTGCAC... |
Task1_train_32972 | Here is a variant on Chromosome 1. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GAAAATGAATGTTTTTTTCTACTAATGAAACTCTGAACTTACAGAAAACTATCTACTTTCAGGCCAGGCATGGTGGCTCATGCCTGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGAGGGTGGATCATGAGGTCAGGAGTTTGAGACCATCCTGGTCAATATGGTGAAACCCCATCTCTACTAAAAATATAAAAAATTAGCCGGGTGCTGTGGCACATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCAGGGAGGCGGAGGTGCAGTGAGCTGAGATTATGCCACTGCACTCCAGCCT... | GAAAATGAATGTTTTTTTCTACTAATGAAACTCTGAACTTACAGAAAACTATCTACTTTCAGGCCAGGCATGGTGGCTCATGCCTGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGAGGGTGGATCATGAGGTCAGGAGTTTGAGACCATCCTGGTCAATATGGTGAAACCCCATCTCTACTAAAAATATAAAAAATTAGCCGGGTGCTGTGGCACATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCAGGGAGGCGGAGGTGCAGTGAGCTGAGATTATGCCACTGCACTCCAGCCT... |
Task1_train_32973 | A mutation on Chromosome 1 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | AAAAAAAAAATCTCAGCTCAAATGAACTCTGTTTTCATGACTGCCACTCTAGGGAACCTCATAAAGAGGGTTACAGGATTCCCTGCACAGGGATGAATAAAACTGGGGTGTCTACTCTGGCTGATTCCATGGGAGAGAAGGGCATACACCTTCATAGACGGTAGTAGAGAAATTCAATTCTGATTTCTCAGAAAGGGAGGTAGATTCACAAAGAGAAACAGGGCTTGAGGCCAAAACCACTTCATCCACAAAAGTAACAATTCTCCAGTGAGTCACAAATCCCCAGCATTTCCCTAGGTAGACAGGAAATAAATGGAAAC... | AAAAAAAAAATCTCAGCTCAAATGAACTCTGTTTTCATGACTGCCACTCTAGGGAACCTCATAAAGAGGGTTACAGGATTCCCTGCACAGGGATGAATAAAACTGGGGTGTCTACTCTGGCTGATTCCATGGGAGAGAAGGGCATACACCTTCATAGACGGTAGTAGAGAAATTCAATTCTGATTTCTCAGAAAGGGAGGTAGATTCACAAAGAGAAACAGGGCTTGAGGCCAAAACCACTTCATCCACAAAAGTAACAATTCTCCAGTGAGTCACAAATCCCCAGCATTTCCCTAGGTAGACAGGAAATAAATGGAAAC... |
Task1_train_32974 | A sequence alteration has been identified on Chromosome 1. Is it disease-inducing or harmless? | Benign | AGAAGGGCATACACCTTCATAGACGGTAGTAGAGAAATTCAATTCTGATTTCTCAGAAAGGGAGGTAGATTCACAAAGAGAAACAGGGCTTGAGGCCAAAACCACTTCATCCACAAAAGTAACAATTCTCCAGTGAGTCACAAATCCCCAGCATTTCCCTAGGTAGACAGGAAATAAATGGAAACCACCACCTTTTCCTATCAGTCTTCAAATTCTATGTGACCATCCTTAGTCCTTAGCCATTTCCTTCCCATATTCCTGCAAACTAACCAAGAATACTTTCCTTAACTACAACTGGATGATCACACCCCTTCCTAACA... | AGAAGGGCATACACCTTCATAGACGGTAGTAGAGAAATTCAATTCTGATTTCTCAGAAAGGGAGGTAGATTCACAAAGAGAAACAGGGCTTGAGGCCAAAACCACTTCATCCACAAAAGTAACAATTCTCCAGTGAGTCACAAATCCCCAGCATTTCCCTAGGTAGACAGGAAATAAATGGAAACCACCACCTTTTCCTATCAGTCTTCAAATTCTATGTGACCATCCTTAGTCCTTAGCCATTTCCTTCCCATATTCCTGCAAACTAACCAAGAATACTTTCCTTAACTACAACTGGATGATCACACCCCTTCCTAACA... |
Task1_train_32975 | This alteration on Chromosome 1 may affect genome function. Does it lead to a disease or is it benign? | Benign | GAAACTAAGGACGCTGGGTAGATGCTACTGCGCAGAAAGGCTCCCTAGGGCCACGTGATTCTTCCCTTCTCAGTCCCTCCTCCGACTCCTCTCCTCTCCCTGTCACTCCTCCCTTCCAGTGATGCTGAGGCTGTTGCTCTGTTCCTTGAGCTTCCAGCATCTCTACTTCTTTTTGGGCTCTGCTTTGCCCTCTATTTGAAGCACAGTCAGTGGTACTCAGCAGTTTCACCTCCTACTCCACCTCCCCATCTGGGGGTCTCTGTAAATCAGTGACCTCTACCCGGAGACAGCTTCCCACTGGGGCTGCACTAAGCACAGAA... | GAAACTAAGGACGCTGGGTAGATGCTACTGCGCAGAAAGGCTCCCTAGGGCCACGTGATTCTTCCCTTCTCAGTCCCTCCTCCGACTCCTCTCCTCTCCCTGTCACTCCTCCCTTCCAGTGATGCTGAGGCTGTTGCTCTGTTCCTTGAGCTTCCAGCATCTCTACTTCTTTTTGGGCTCTGCTTTGCCCTCTATTTGAAGCACAGTCAGTGGTACTCAGCAGTTTCACCTCCTACTCCACCTCCCCATCTGGGGGTCTCTGTAAATCAGTGACCTCTACCCGGAGACAGCTTCCCACTGGGGCTGCACTAAGCACAGAA... |
Task1_train_32976 | A variant affecting Chromosome 1 has been observed. Determine if it's benign or associated with disease. | Benign | GCCGAGATTGTGCCATCGTACTCCCGCCCAGGCGACAGTGTGAGACTCTGTCTCAAAAAAAAAAAAAAAAAGCCTGGTGCAGGCTCCCTGTCTCCCTTGGCAGCAGCGCTGAGTTCCTGAGTTCCTGAGGCCACCCCGCCTCCGCACACCCCCCTACCTCTATCTCCTTCCTTCCCCGGCCTGGCAGTCGGCCCCACCCCCTCCCATCTCCCTGCCTCTGTCCAGCATTTCTCCTCGCCTTTTTTCACAAGGCGGTTCCCTTTTCCTTTGTTCTCTCCTGGTTTCTTTACAGTGTTTCCTTTCATGCTTCAGGCTTCTTC... | GCCGAGATTGTGCCATCGTACTCCCGCCCAGGCGACAGTGTGAGACTCTGTCTCAAAAAAAAAAAAAAAAAGCCTGGTGCAGGCTCCCTGTCTCCCTTGGCAGCAGCGCTGAGTTCCTGAGTTCCTGAGGCCACCCCGCCTCCGCACACCCCCCTACCTCTATCTCCTTCCTTCCCCGGCCTGGCAGTCGGCCCCACCCCCTCCCATCTCCCTGCCTCTGTCCAGCATTTCTCCTCGCCTTTTTTCACAAGGCGGTTCCCTTTTCCTTTGTTCTCTCCTGGTTTCTTTACAGTGTTTCCTTTCATGCTTCAGGCTTCTTC... |
Task1_train_32977 | Given this variant on Chromosome 1, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CAATGTCAGGGGATTCCCAGGTTATGTCTTTGGTGGGCATCTGCCATTTGTTAAAGTGAGAGAGAGAGAAGCTGTGCTTCTTGAAGAAAATGCCATCTTACTCTATCAGAATGATACTCAGGAGCCATAAGCCTAGCTTGTCTCCACCACTGATCAAAATGTTGAGTGACTATAACTTTAGGGCATCTTCTCATCATGATCTTAGAAATGACATTGTTTTGATCAGGGCCTTCTTGGGCTTATTTCTAGTTAGTAAACTATGAATACTAAAAATAAGAATCCAGCAGGCAGCACAGGCGTGTTTGTTATTATCTAATAAA... | CAATGTCAGGGGATTCCCAGGTTATGTCTTTGGTGGGCATCTGCCATTTGTTAAAGTGAGAGAGAGAGAAGCTGTGCTTCTTGAAGAAAATGCCATCTTACTCTATCAGAATGATACTCAGGAGCCATAAGCCTAGCTTGTCTCCACCACTGATCAAAATGTTGAGTGACTATAACTTTAGGGCATCTTCTCATCATGATCTTAGAAATGACATTGTTTTGATCAGGGCCTTCTTGGGCTTATTTCTAGTTAGTAAACTATGAATACTAAAAATAAGAATCCAGCAGGCAGCACAGGCGTGTTTGTTATTATCTAATAAA... |
Task1_train_32978 | This mutation is located on Chromosome 1. Is it associated with a disease or is it a benign polymorphism? | Benign | GAGTTTGGAGTGTCCAGAAAGGCTGCTTAGAAGAGGTGATGTTTTAGTTGGGATCCAGAGGATGCCTAGGTTTTTGTCAGGCAGAAAACAGCGGGGAGGTATTCCATGCTGATGGGATGGCATATTCAAAGATATGAATTCATGAAAGATCAAGTGTACCAAGAAAAGGCCAAGTCCTTGGTGTGGCTGGAGCATTGGATGCTCCTGGGAGGGGCCTGTCATGTGAGTAGGCTGGGTAGGTCATCTGATCAGATAGTGAGGCCTATGTGCCACACTGAGGGATGTAAATTTTTTTCTCAAGTCACTGGGGAGCCACTGAG... | GAGTTTGGAGTGTCCAGAAAGGCTGCTTAGAAGAGGTGATGTTTTAGTTGGGATCCAGAGGATGCCTAGGTTTTTGTCAGGCAGAAAACAGCGGGGAGGTATTCCATGCTGATGGGATGGCATATTCAAAGATATGAATTCATGAAAGATCAAGTGTACCAAGAAAAGGCCAAGTCCTTGGTGTGGCTGGAGCATTGGATGCTCCTGGGAGGGGCCTGTCATGTGAGTAGGCTGGGTAGGTCATCTGATCAGATAGTGAGGCCTATGTGCCACACTGAGGGATGTAAATTTTTTTCTCAAGTCACTGGGGAGCCACTGAG... |
Task1_train_32979 | This variant lies on Chromosome 1. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TTGCTCATCAATTATTTATTAGATATTTTAATACAATTCATAATCTGCACATAGATTTTCTTGAGAAGAGTTTTCAGGTCTTAGGAGCTATGAATCAATAGTCTTGATCCCCTGGAATTTGCAAACATATGACATATACTTTCTCTTTATTTTATATAATCAGAAACTAGAAAGGTATTGAATTGGAATGGGTCCATTCAGCTCTAGTGATAGGCACTAATGGACAGTCCCTCTGGTGTGGAATAAGAGCCTGGCATGGGAGATGTAGTAAACATCAGAGATGCACTCTATGTTCTCGGCTCTTGTAGCAGCCTTGAACT... | TTGCTCATCAATTATTTATTAGATATTTTAATACAATTCATAATCTGCACATAGATTTTCTTGAGAAGAGTTTTCAGGTCTTAGGAGCTATGAATCAATAGTCTTGATCCCCTGGAATTTGCAAACATATGACATATACTTTCTCTTTATTTTATATAATCAGAAACTAGAAAGGTATTGAATTGGAATGGGTCCATTCAGCTCTAGTGATAGGCACTAATGGACAGTCCCTCTGGTGTGGAATAAGAGCCTGGCATGGGAGATGTAGTAAACATCAGAGATGCACTCTATGTTCTCGGCTCTTGTAGCAGCCTTGAACT... |
Task1_train_32980 | A genetic alteration is present on Chromosome 1. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GTCCTGATCTAGAGCCGTGTTGTCCGTAGCCAGAGGAGTGACCTGAGCCAGACCCATGCTGACTGTAACTAGAGGACTGCCCTGAGCTAGACTCGTGGTGACCAAAGCCAGAAGACTCGCCTAAGCCAGACCCATGTTGGCCACTGCTGGAAGACCGACCGGAGCCAGACCCATGTCGGCCGTAGCTGGGAGACTGCCTTGACCCAGACCCACGCTGGCCGTGGCCTGGAGACTGGCCAGATCCAGAGCCCTGTCGGCCATAGCCAGAAGACTGACTTGAGCCAGAGCCATGCTGACCGTGGCTGGAAGACTGACCTGAG... | GTCCTGATCTAGAGCCGTGTTGTCCGTAGCCAGAGGAGTGACCTGAGCCAGACCCATGCTGACTGTAACTAGAGGACTGCCCTGAGCTAGACTCGTGGTGACCAAAGCCAGAAGACTCGCCTAAGCCAGACCCATGTTGGCCACTGCTGGAAGACCGACCGGAGCCAGACCCATGTCGGCCGTAGCTGGGAGACTGCCTTGACCCAGACCCACGCTGGCCGTGGCCTGGAGACTGGCCAGATCCAGAGCCCTGTCGGCCATAGCCAGAAGACTGACTTGAGCCAGAGCCATGCTGACCGTGGCTGGAAGACTGACCTGAG... |
Task1_train_32981 | A variant has been detected on Chromosome 1. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | ATCTAGAGCCGTGTTGTCCGTAGCCAGAGGAGTGACCTGAGCCAGACCCATGCTGACTGTAACTAGAGGACTGCCCTGAGCTAGACTCGTGGTGACCAAAGCCAGAAGACTCGCCTAAGCCAGACCCATGTTGGCCACTGCTGGAAGACCGACCGGAGCCAGACCCATGTCGGCCGTAGCTGGGAGACTGCCTTGACCCAGACCCACGCTGGCCGTGGCCTGGAGACTGGCCAGATCCAGAGCCCTGTCGGCCATAGCCAGAAGACTGACTTGAGCCAGAGCCATGCTGACCGTGGCTGGAAGACTGACCTGAGCTAGCT... | ATCTAGAGCCGTGTTGTCCGTAGCCAGAGGAGTGACCTGAGCCAGACCCATGCTGACTGTAACTAGAGGACTGCCCTGAGCTAGACTCGTGGTGACCAAAGCCAGAAGACTCGCCTAAGCCAGACCCATGTTGGCCACTGCTGGAAGACCGACCGGAGCCAGACCCATGTCGGCCGTAGCTGGGAGACTGCCTTGACCCAGACCCACGCTGGCCGTGGCCTGGAGACTGGCCAGATCCAGAGCCCTGTCGGCCATAGCCAGAAGACTGACTTGAGCCAGAGCCATGCTGACCGTGGCTGGAAGACTGACCTGAGCTAGCT... |
Task1_train_32982 | This variant is found on Chromosome 1. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TGAGCTAGACTCGTGGTGACCAAAGCCAGAAGACTCGCCTAAGCCAGACCCATGTTGGCCACTGCTGGAAGACCGACCGGAGCCAGACCCATGTCGGCCGTAGCTGGGAGACTGCCTTGACCCAGACCCACGCTGGCCGTGGCCTGGAGACTGGCCAGATCCAGAGCCCTGTCGGCCATAGCCAGAAGACTGACTTGAGCCAGAGCCATGCTGACCGTGGCTGGAAGACTGACCTGAGCTAGCTCCATGTTGGCCACAGCTCGATGACTGTCCTGATGTAGAACCGTGTTGCCCATGGGTAGAGGAATGACCTGAGCTAG... | TGAGCTAGACTCGTGGTGACCAAAGCCAGAAGACTCGCCTAAGCCAGACCCATGTTGGCCACTGCTGGAAGACCGACCGGAGCCAGACCCATGTCGGCCGTAGCTGGGAGACTGCCTTGACCCAGACCCACGCTGGCCGTGGCCTGGAGACTGGCCAGATCCAGAGCCCTGTCGGCCATAGCCAGAAGACTGACTTGAGCCAGAGCCATGCTGACCGTGGCTGGAAGACTGACCTGAGCTAGCTCCATGTTGGCCACAGCTCGATGACTGTCCTGATGTAGAACCGTGTTGCCCATGGGTAGAGGAATGACCTGAGCTAG... |
Task1_train_32983 | A variant affecting Chromosome 1 has been observed. Determine if it's benign or associated with disease. | Benign | TTGAGCCAGAGCCATGCTGACCGTGGCTGGAAGACTGACCTGAGCTAGCTCCATGTTGGCCACAGCTCGATGACTGTCCTGATGTAGAACCGTGTTGCCCATGGGTAGAGGAATGACCTGAGCTAGATCCATGTTGACCGTAGCCAGAGGACTGTCCTGAGCGAGACTCTCGGTGACCTAAGCCAGAAGAGTGACCGGAGCCAGACTCATATGGGCCACGGCTTGAAGACCACCCTGAGCCAGACCTATATGGGCCATAGCTGGAAGACTGCCCGGAACCAGACCCATGTCGGCCACGGCTAGGGCTAGGAGACTGGCCA... | TTGAGCCAGAGCCATGCTGACCGTGGCTGGAAGACTGACCTGAGCTAGCTCCATGTTGGCCACAGCTCGATGACTGTCCTGATGTAGAACCGTGTTGCCCATGGGTAGAGGAATGACCTGAGCTAGATCCATGTTGACCGTAGCCAGAGGACTGTCCTGAGCGAGACTCTCGGTGACCTAAGCCAGAAGAGTGACCGGAGCCAGACTCATATGGGCCACGGCTTGAAGACCACCCTGAGCCAGACCTATATGGGCCATAGCTGGAAGACTGCCCGGAACCAGACCCATGTCGGCCACGGCTAGGGCTAGGAGACTGGCCA... |
Task1_train_32984 | A variant found on Chromosome 1 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GTCGGCCGTGGCCCGAAGATTGATGGGAGCCCGACCCATGCTGACCATAGCTGGAAGACAAACCTGAGCTAGATCCGTGTTGTTCACTCCTAGATGACTGTCCTGACCTAGAGCCGTGTTTTCTGTAGCCGGAGGAGTGACTTGAGCCAGATCCATGCTGACTGTAACCAGAGGACTGCCCTGAGCCAGACTTGTGACCAAAGCCGGAAGACTGGCCTGAGACAGACCCATGTGGGCCATTGCTTGAAGACCAACCGGAGCCAGACCCATGTTGGCCGTAGCTGGAAGAGTGCCCAAAATCGGACCCATGTCGGCCGCGA... | GTCGGCCGTGGCCCGAAGATTGATGGGAGCCCGACCCATGCTGACCATAGCTGGAAGACAAACCTGAGCTAGATCCGTGTTGTTCACTCCTAGATGACTGTCCTGACCTAGAGCCGTGTTTTCTGTAGCCGGAGGAGTGACTTGAGCCAGATCCATGCTGACTGTAACCAGAGGACTGCCCTGAGCCAGACTTGTGACCAAAGCCGGAAGACTGGCCTGAGACAGACCCATGTGGGCCATTGCTTGAAGACCAACCGGAGCCAGACCCATGTTGGCCGTAGCTGGAAGAGTGCCCAAAATCGGACCCATGTCGGCCGCGA... |
Task1_train_32985 | This variant is present on Chromosome 1. Is the change likely to result in a pathogenic outcome? | Benign | ACAGGAGCTACAGGAGGTAGCCACATAAGCTGGTTGTGAGACTGGGGGCAAGGTAGCAAAGTGTATCAGAGAAATGGACAAAGGCATCCTCTCTAGGTATGTCTGTGGAAGTTCAATGAGGTCTGAAGGTATGATATCTTATGGAGTTTGCAGCTTTGTAGGGGCATTTGGGGACAACACTTCAAGCAGGGAGGGATGACACTGGTGGGAAGGAAATGCCATCTTCAAGTGGCTTGTGGAGAACACATATAGACTATTGTTTGAGGCTAATTAGAAAAACGAGCTTGTTTGTTGCTTTTCATTCAGTCCCTGCACCTATT... | ACAGGAGCTACAGGAGGTAGCCACATAAGCTGGTTGTGAGACTGGGGGCAAGGTAGCAAAGTGTATCAGAGAAATGGACAAAGGCATCCTCTCTAGGTATGTCTGTGGAAGTTCAATGAGGTCTGAAGGTATGATATCTTATGGAGTTTGCAGCTTTGTAGGGGCATTTGGGGACAACACTTCAAGCAGGGAGGGATGACACTGGTGGGAAGGAAATGCCATCTTCAAGTGGCTTGTGGAGAACACATATAGACTATTGTTTGAGGCTAATTAGAAAAACGAGCTTGTTTGTTGCTTTTCATTCAGTCCCTGCACCTATT... |
Task1_train_32986 | This sequence change occurs on Chromosome 1. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TAGAACTTCATTCATATTTTTACTATTCTTTTTTCAGCATTTTCATCTACTTGCTTAAATTACAAAGATACAAATATTTTCCTTCCAGGTCAGGAGGACACTTCTTTTTAATTCTTTTCCCTTTTTCAGGATATATCAGCACAACTTCTCTGCTCCAACTAGTCTACATTGCAAAGCATCTCCTAGTGTCTTTGGAAGAAGGATCTATGGTCAGTAATTCCTGTTTCGTGATCTGCCTTTGACATGGCTTAATCACCACCTAAGTTGATAATTCCATATTAATAATAGTGATATTCATGATTGAGCAGAGCATGTTTTTT... | TAGAACTTCATTCATATTTTTACTATTCTTTTTTCAGCATTTTCATCTACTTGCTTAAATTACAAAGATACAAATATTTTCCTTCCAGGTCAGGAGGACACTTCTTTTTAATTCTTTTCCCTTTTTCAGGATATATCAGCACAACTTCTCTGCTCCAACTAGTCTACATTGCAAAGCATCTCCTAGTGTCTTTGGAAGAAGGATCTATGGTCAGTAATTCCTGTTTCGTGATCTGCCTTTGACATGGCTTAATCACCACCTAAGTTGATAATTCCATATTAATAATAGTGATATTCATGATTGAGCAGAGCATGTTTTTT... |
Task1_train_32987 | A sequence alteration has been identified on Chromosome 1. Is it disease-inducing or harmless? | Benign | CCTGCATGTGATTGTGGGACAGTGATTATGTTGGAGAAAAATATAGGCCTTGATTAAATTTTGTCTTTCATTATTAATTACTTGTTATTTTGAATGTAATGTATCTGCTTTATGGTCATATAGCTTTCCAATGATATAGAAGACATCTAATTCTGGCCATGGGGAAGTATGTAATTTGTGTTTATGACAAATAAGAATACAAGAGACAAACAGTATTATATGATGAATAGTTTATTTTTAATTTAGATGCAGCTTACTATAATATTAATTATGTCCAAGATGATTTTTTGAATACAGAATACTAGAATTCCAATAGAAGG... | CCTGCATGTGATTGTGGGACAGTGATTATGTTGGAGAAAAATATAGGCCTTGATTAAATTTTGTCTTTCATTATTAATTACTTGTTATTTTGAATGTAATGTATCTGCTTTATGGTCATATAGCTTTCCAATGATATAGAAGACATCTAATTCTGGCCATGGGGAAGTATGTAATTTGTGTTTATGACAAATAAGAATACAAGAGACAAACAGTATTATATGATGAATAGTTTATTTTTAATTTAGATGCAGCTTACTATAATATTAATTATGTCCAAGATGATTTTTTGAATACAGAATACTAGAATTCCAATAGAAGG... |
Task1_train_32988 | Given a variant located on Chromosome 1, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CATTACACAATAAAAATAAGCTACCACCAAACTAATGAAATACTATAGCATATTTTAAACAGATTGACAGGAAAAGATAACTTCCCTGAAAGTATTATGAAGTTTCTTGATTGAAAGTGAACTTGCTTCATTCTTCTATTCTTGGATTAATTCCTTTGCCATTAATTTCTTACTCATAGTAATAGTATCTCTGTGACTGACTAAATCCCAGTTGTTTCGATATATCACTAGAATGGCCACATAAACCTGGGTCCTTATTAATATACGTTGCATAATACCTTGGATGATCTTTACCAAACGCACTTGCTTTACAGATATCA... | CATTACACAATAAAAATAAGCTACCACCAAACTAATGAAATACTATAGCATATTTTAAACAGATTGACAGGAAAAGATAACTTCCCTGAAAGTATTATGAAGTTTCTTGATTGAAAGTGAACTTGCTTCATTCTTCTATTCTTGGATTAATTCCTTTGCCATTAATTTCTTACTCATAGTAATAGTATCTCTGTGACTGACTAAATCCCAGTTGTTTCGATATATCACTAGAATGGCCACATAAACCTGGGTCCTTATTAATATACGTTGCATAATACCTTGGATGATCTTTACCAAACGCACTTGCTTTACAGATATCA... |
Task1_train_32989 | The following genetic variant occurs on Chromosome 1. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GTCTTCTGAATGTCCCTCACTGTCACTGTCCTGGCTCACACTGGATCCCTGGCGCCTGCTTCTCCTGGACCCCTCTGATTGTCCCTGGACTGCCTGTGAGTGTCTAGAGATGTCGGCATGAGTGGAAGCTTCATGGTGACGTGACACTGAGTGCCTGGAGCTGTCTCCTGATTGTTCCTCATTACGTGTTGTTCTGCTTGCACTTCTGGATCCTGACTGCCCACGGGAGGCATCAGACCTTCCCTGGGATGTGGTGTGGCTGTGATGGGACCCTGAGTGTCCAGAGCTATCTACCGAATGCTCGTGGTGGTACCCCTGCC... | GTCTTCTGAATGTCCCTCACTGTCACTGTCCTGGCTCACACTGGATCCCTGGCGCCTGCTTCTCCTGGACCCCTCTGATTGTCCCTGGACTGCCTGTGAGTGTCTAGAGATGTCGGCATGAGTGGAAGCTTCATGGTGACGTGACACTGAGTGCCTGGAGCTGTCTCCTGATTGTTCCTCATTACGTGTTGTTCTGCTTGCACTTCTGGATCCTGACTGCCCACGGGAGGCATCAGACCTTCCCTGGGATGTGGTGTGGCTGTGATGGGACCCTGAGTGTCCAGAGCTATCTACCGAATGCTCGTGGTGGTACCCCTGCC... |
Task1_train_32990 | A change on Chromosome 1 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TCGGCATGAGTGGAAGCTTCATGGTGACGTGACACTGAGTGCCTGGAGCTGTCTCCTGATTGTTCCTCATTACGTGTTGTTCTGCTTGCACTTCTGGATCCTGACTGCCCACGGGAGGCATCAGACCTTCCCTGGGATGTGGTGTGGCTGTGATGGGACCCTGAGTGTCCAGAGCTATCTACCGAATGCTCGTGGTGGTACCCCTGCCTTCCTCCTCTGCTTGACCCCGGGTGTCCACGAATGGTGTCCTGACCGTATTGGGATGCTGAGTGCCTGGAGCTGTCTTGTGCCTGCTCATGGCGGGATCCTTGTCTTCCTCT... | TCGGCATGAGTGGAAGCTTCATGGTGACGTGACACTGAGTGCCTGGAGCTGTCTCCTGATTGTTCCTCATTACGTGTTGTTCTGCTTGCACTTCTGGATCCTGACTGCCCACGGGAGGCATCAGACCTTCCCTGGGATGTGGTGTGGCTGTGATGGGACCCTGAGTGTCCAGAGCTATCTACCGAATGCTCGTGGTGGTACCCCTGCCTTCCTCCTCTGCTTGACCCCGGGTGTCCACGAATGGTGTCCTGACCGTATTGGGATGCTGAGTGCCTGGAGCTGTCTTGTGCCTGCTCATGGCGGGATCCTTGTCTTCCTCT... |
Task1_train_32991 | A genetic alteration is present on Chromosome 1. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GTGGTGGTACCCCTGCCTTCCTCCTCTGCTTGACCCCGGGTGTCCACGAATGGTGTCCTGACCGTATTGGGATGCTGAGTGCCTGGAGCTGTCTTGTGCCTGCTCATGGCGGGATCCTTGTCTTCCTCTAGTGCTGGGCCCCGTCCATCCATGGGAGGACTCAGACTGTTCATGAGTGCTCACCTGGTAGAGGAAAGATCCTGAATGTCCAGACGTTTCCCCTGACCGGCCACGTGCGGACTCTTGGTGGCTCTGCTGATGGGACCCAGCCTGTCCGTGGGCTGACACTGACTGTGTGTCTGAGTCTTCTGAATGTCCCT... | GTGGTGGTACCCCTGCCTTCCTCCTCTGCTTGACCCCGGGTGTCCACGAATGGTGTCCTGACCGTATTGGGATGCTGAGTGCCTGGAGCTGTCTTGTGCCTGCTCATGGCGGGATCCTTGTCTTCCTCTAGTGCTGGGCCCCGTCCATCCATGGGAGGACTCAGACTGTTCATGAGTGCTCACCTGGTAGAGGAAAGATCCTGAATGTCCAGACGTTTCCCCTGACCGGCCACGTGCGGACTCTTGGTGGCTCTGCTGATGGGACCCAGCCTGTCCGTGGGCTGACACTGACTGTGTGTCTGAGTCTTCTGAATGTCCCT... |
Task1_train_32992 | A mutation found on Chromosome 1 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CCCCGTCCATCCATGGGAGGACTCAGACTGTTCATGAGTGCTCACCTGGTAGAGGAAAGATCCTGAATGTCCAGACGTTTCCCCTGACCGGCCACGTGCGGACTCTTGGTGGCTCTGCTGATGGGACCCAGCCTGTCCGTGGGCTGACACTGACTGTGTGTCTGAGTCTTCTGAATGTCCCTCATTGTCACTGGCCTGACTACCACTGTACCCTCGGTGTCCACTGTCTCTGACTGCAGATGAAGCTTGTCCGTGCCCAATGCCTGAGTGTCTGGAGCTGTCTGCTGACTGCTGGTGGTGGGATCCATGTCTTTCTCCTG... | CCCCGTCCATCCATGGGAGGACTCAGACTGTTCATGAGTGCTCACCTGGTAGAGGAAAGATCCTGAATGTCCAGACGTTTCCCCTGACCGGCCACGTGCGGACTCTTGGTGGCTCTGCTGATGGGACCCAGCCTGTCCGTGGGCTGACACTGACTGTGTGTCTGAGTCTTCTGAATGTCCCTCATTGTCACTGGCCTGACTACCACTGTACCCTCGGTGTCCACTGTCTCTGACTGCAGATGAAGCTTGTCCGTGCCCAATGCCTGAGTGTCTGGAGCTGTCTGCTGACTGCTGGTGGTGGGATCCATGTCTTTCTCCTG... |
Task1_train_32993 | A mutation on Chromosome 1 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GTGCGGACTCTTGGTGGCTCTGCTGATGGGACCCAGCCTGTCCGTGGGCTGACACTGACTGTGTGTCTGAGTCTTCTGAATGTCCCTCATTGTCACTGGCCTGACTACCACTGTACCCTCGGTGTCCACTGTCTCTGACTGCAGATGAAGCTTGTCCGTGCCCAATGCCTGAGTGTCTGGAGCTGTCTGCTGACTGCTGGTGGTGGGATCCATGTCTTTCTCCTGCACTTGATCTTGCCTGTTCATGGGATGATGCAGCCTGTCCACCAGAGGAAGTCTGTGTGTGACGAGTGCCTGATTGTCTGGAGCTGTCTGCAGAG... | GTGCGGACTCTTGGTGGCTCTGCTGATGGGACCCAGCCTGTCCGTGGGCTGACACTGACTGTGTGTCTGAGTCTTCTGAATGTCCCTCATTGTCACTGGCCTGACTACCACTGTACCCTCGGTGTCCACTGTCTCTGACTGCAGATGAAGCTTGTCCGTGCCCAATGCCTGAGTGTCTGGAGCTGTCTGCTGACTGCTGGTGGTGGGATCCATGTCTTTCTCCTGCACTTGATCTTGCCTGTTCATGGGATGATGCAGCCTGTCCACCAGAGGAAGTCTGTGTGTGACGAGTGCCTGATTGTCTGGAGCTGTCTGCAGAG... |
Task1_train_32994 | This mutation is located on Chromosome 1. Is it associated with a disease or is it a benign polymorphism? | Benign | TGGATCCTGACTGCCCACGGGAGGCATCAGACCTTCCCTGGGATGTGGTGTGGCTGTGATGGGACCCTGAGTGTCCAGAGCTATCTACCGAATGCTCGTGGTGGTACCCCTGCCTTCCTCCTCTGCTTGACCCCGGGTGTCCACGAATGGTGTCCTGACCGTCTTGGGATGCTGAGTGCCTGGAGCTGTCTTGTGCCTGCTCATGGCGGGATCCTTGTCTTCCTCTAGTGCTGGGCCCCGTCCATCCATGGGAGGACTCAGACTGTTCATGAGTGCTCACCTGGTAGAGGAAAGATCCTGAATGTCCAGACGTTTCCCCT... | TGGATCCTGACTGCCCACGGGAGGCATCAGACCTTCCCTGGGATGTGGTGTGGCTGTGATGGGACCCTGAGTGTCCAGAGCTATCTACCGAATGCTCGTGGTGGTACCCCTGCCTTCCTCCTCTGCTTGACCCCGGGTGTCCACGAATGGTGTCCTGACCGTCTTGGGATGCTGAGTGCCTGGAGCTGTCTTGTGCCTGCTCATGGCGGGATCCTTGTCTTCCTCTAGTGCTGGGCCCCGTCCATCCATGGGAGGACTCAGACTGTTCATGAGTGCTCACCTGGTAGAGGAAAGATCCTGAATGTCCAGACGTTTCCCCT... |
Task1_train_32995 | A sequence alteration has been identified on Chromosome 1. Is it disease-inducing or harmless? | Benign | TTCATGAGTGCTCACCTGGTAGAGGAAAGATCCTGAATGTCCAGACGTTTCCCCTGACCGGCCACGTGCGGACTCTTGGTGGCTCTGCTGATGGGACCCAGCCTGTCCGTGGGCTGACACTGACTGTGTGTCTGAGTCTTCTGAATGTCCCTCATTGTCACTGGCCTGACTACCACTGTACCCTCGGTGTCCACTGTCTCTGACTGCAGATGAAGCTTGTCCGTGCCCAATGCCTGAGTGTCTGGAGCTGTCTGCTGACTGCTGGTGGTGGGATCCATGTCTTTCTCCTGCACTTGATCTTGCCTGTTCATGGGATGATG... | TTCATGAGTGCTCACCTGGTAGAGGAAAGATCCTGAATGTCCAGACGTTTCCCCTGACCGGCCACGTGCGGACTCTTGGTGGCTCTGCTGATGGGACCCAGCCTGTCCGTGGGCTGACACTGACTGTGTGTCTGAGTCTTCTGAATGTCCCTCATTGTCACTGGCCTGACTACCACTGTACCCTCGGTGTCCACTGTCTCTGACTGCAGATGAAGCTTGTCCGTGCCCAATGCCTGAGTGTCTGGAGCTGTCTGCTGACTGCTGGTGGTGGGATCCATGTCTTTCTCCTGCACTTGATCTTGCCTGTTCATGGGATGATG... |
Task1_train_32996 | This mutation occurs on Chromosome 1. Does this change lead to a known medical condition, or is it benign? | Benign | ACCGGCCACGTGCGGACTCTTGGTGGCTCTGCTGATGGGACCCAGCCTGTCCGTGGGCTGACACTGACTGTGTGTCTGAGTCTTCTGAATGTCCCTCATTGTCACTGGCCTGACTACCACTGTACCCTCGGTGTCCACTGTCTCTGACTGCAGATGAAGCTTGTCCGTGCCCAATGCCTGAGTGTCTGGAGCTGTCTGCTGACTGCTGGTGGTGGGATCCATGTCTTTCTCCTGCACTTGATCTTGCCTGTTCATGGGATGATGCAGCCTGTCCACCAGAGGAAGTCTGTGTGTGACGAGTGCCTGATTGTCTGGAGCTG... | ACCGGCCACGTGCGGACTCTTGGTGGCTCTGCTGATGGGACCCAGCCTGTCCGTGGGCTGACACTGACTGTGTGTCTGAGTCTTCTGAATGTCCCTCATTGTCACTGGCCTGACTACCACTGTACCCTCGGTGTCCACTGTCTCTGACTGCAGATGAAGCTTGTCCGTGCCCAATGCCTGAGTGTCTGGAGCTGTCTGCTGACTGCTGGTGGTGGGATCCATGTCTTTCTCCTGCACTTGATCTTGCCTGTTCATGGGATGATGCAGCCTGTCCACCAGAGGAAGTCTGTGTGTGACGAGTGCCTGATTGTCTGGAGCTG... |
Task1_train_32997 | This mutation occurs on Chromosome 1. Does this change lead to a known medical condition, or is it benign? | Benign | CCTGAGCAGATCCATGATGGTTTCTGGAAGCAGACCCAGACCACCTCTCAGAGTCTTCTGAGTGTCCCTGACTGTCACTGTCCTGGCTAAAACTGGATCCCCAGTTCCTGCTTGTCCTGGGCCCCTCTGATTGTCCCTGGCCCACCTGCGAGTGTCCAGAGCTGTCGGCCCGAGAGGAAGCTTCATGGTGACGCGACCCTGAGTGCCTGGAGCCGTCTCCTGATTGTTCATCGTTACGAGTTTGTCTGCTTGCACTTCTGGATCCTGAGTGCCCATGGGAGGCATCAGACCTTCCCTGGGATGTGGTGTGGCTGTGATGA... | CCTGAGCAGATCCATGATGGTTTCTGGAAGCAGACCCAGACCACCTCTCAGAGTCTTCTGAGTGTCCCTGACTGTCACTGTCCTGGCTAAAACTGGATCCCCAGTTCCTGCTTGTCCTGGGCCCCTCTGATTGTCCCTGGCCCACCTGCGAGTGTCCAGAGCTGTCGGCCCGAGAGGAAGCTTCATGGTGACGCGACCCTGAGTGCCTGGAGCCGTCTCCTGATTGTTCATCGTTACGAGTTTGTCTGCTTGCACTTCTGGATCCTGAGTGCCCATGGGAGGCATCAGACCTTCCCTGGGATGTGGTGTGGCTGTGATGA... |
Task1_train_32998 | A variant on Chromosome 1 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GACTGTCACTGTCCTGGCTAAAACTGGATCCCCAGTTCCTGCTTGTCCTGGGCCCCTCTGATTGTCCCTGGCCCACCTGCGAGTGTCCAGAGCTGTCGGCCCGAGAGGAAGCTTCATGGTGACGCGACCCTGAGTGCCTGGAGCCGTCTCCTGATTGTTCATCGTTACGAGTTTGTCTGCTTGCACTTCTGGATCCTGAGTGCCCATGGGAGGCATCAGACCTTCCCTGGGATGTGGTGTGGCTGTGATGAGACCCTGAGTGTCCAGATCTATCTACCAATTGCTCGTAGTGGGATCCCTGCCTTCCTCCACTGCTTGAC... | GACTGTCACTGTCCTGGCTAAAACTGGATCCCCAGTTCCTGCTTGTCCTGGGCCCCTCTGATTGTCCCTGGCCCACCTGCGAGTGTCCAGAGCTGTCGGCCCGAGAGGAAGCTTCATGGTGACGCGACCCTGAGTGCCTGGAGCCGTCTCCTGATTGTTCATCGTTACGAGTTTGTCTGCTTGCACTTCTGGATCCTGAGTGCCCATGGGAGGCATCAGACCTTCCCTGGGATGTGGTGTGGCTGTGATGAGACCCTGAGTGTCCAGATCTATCTACCAATTGCTCGTAGTGGGATCCCTGCCTTCCTCCACTGCTTGAC... |
Task1_train_32999 | Consider this mutation on Chromosome 1. Is this a benign change or a disease-causing variant? | Benign | AGTGTCCAGATCTATCTACCAATTGCTCGTAGTGGGATCCCTGCCTTCCTCCACTGCTTGACCCCGGGTGTCCATGAATGGTGTCCTGACCCTCTTGGGACGTTGAGTGCCTGGAGCTGTCTCGTGCCTGCTTGTGGTGGGATCCTTGTCTTCCTCCAGTGCTGGTCCCGGTCCGTCCATGGGCGGACTCAGACTGTTCATGAGTGCTCACCTGGTAGAGGAAAGACCCTGAACGTCCAGACCTTCCTGCTGACCGGCCACGTGTGGACTCTTGGTGGCTCTGCTGATGGGGCCCAGCCTGTCCGTGGGCTGACACTGAC... | AGTGTCCAGATCTATCTACCAATTGCTCGTAGTGGGATCCCTGCCTTCCTCCACTGCTTGACCCCGGGTGTCCATGAATGGTGTCCTGACCCTCTTGGGACGTTGAGTGCCTGGAGCTGTCTCGTGCCTGCTTGTGGTGGGATCCTTGTCTTCCTCCAGTGCTGGTCCCGGTCCGTCCATGGGCGGACTCAGACTGTTCATGAGTGCTCACCTGGTAGAGGAAAGACCCTGAACGTCCAGACCTTCCTGCTGACCGGCCACGTGTGGACTCTTGGTGGCTCTGCTGATGGGGCCCAGCCTGTCCGTGGGCTGACACTGAC... |
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