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_32600 | A mutation on Chromosome 1 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TGGGCAGTCTGTCACAGAGTAGGGGGGCTGAGCTGAGTCTTGAAGGATGAGCAGGTGTTCAGTGGTGGAAAAGTGGGCAGGGGCACTCCTGGGTGAAGGAGCAGCATGGGCACACCTCCAGAGATGTGAATGAGCAGGGTCTGTTCAGGAGTACGGACTAGGCAAAAGGGAAAAGTGTGTGGAGGACGAGGAGGGAAGTAAGGCTGGAAGTAGATGCAGGCCAGATGGTGGGAAGCCCCACAGGGCCTGGGGCCTGGGAAACACTTGTCAGCACTTGAAGGAAGGTAATTAAATAAAAGACAGATTGTTGGAGCCAAAGA... | TGGGCAGTCTGTCACAGAGTAGGGGGGCTGAGCTGAGTCTTGAAGGATGAGCAGGTGTTCAGTGGTGGAAAAGTGGGCAGGGGCACTCCTGGGTGAAGGAGCAGCATGGGCACACCTCCAGAGATGTGAATGAGCAGGGTCTGTTCAGGAGTACGGACTAGGCAAAAGGGAAAAGTGTGTGGAGGACGAGGAGGGAAGTAAGGCTGGAAGTAGATGCAGGCCAGATGGTGGGAAGCCCCACAGGGCCTGGGGCCTGGGAAACACTTGTCAGCACTTGAAGGAAGGTAATTAAATAAAAGACAGATTGTTGGAGCCAAAGA... |
Task1_train_32601 | Chromosome 1 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AGGTGGCACTAGAGTTGATCCAAAAGGAGATTTAAATAGGTAGTGCTGGCCAGGGCAAGGGCCTAAGGAAATGGTGTGGTGGTAGGACCACGGCTGGTCACCAGAGGCTGTGAGGCTGTCGGGGTGGCTACAAGGCAGAGCCCAGCTTGGAGATGATGCTGGGCAGGGAGGACAGGCCAGCCTTGACTGCCAGGATAAGGAGGTGATTTGATGTTGAGAGTAGGTGGGAGTCATTGAGTATTTTATTTTATTTTATTTTACTTTTTCCTTTACAGAGGTACTCAAGTTAAAGCCATTGAGTATTCTTTAGCCAAGGCCAT... | AGGTGGCACTAGAGTTGATCCAAAAGGAGATTTAAATAGGTAGTGCTGGCCAGGGCAAGGGCCTAAGGAAATGGTGTGGTGGTAGGACCACGGCTGGTCACCAGAGGCTGTGAGGCTGTCGGGGTGGCTACAAGGCAGAGCCCAGCTTGGAGATGATGCTGGGCAGGGAGGACAGGCCAGCCTTGACTGCCAGGATAAGGAGGTGATTTGATGTTGAGAGTAGGTGGGAGTCATTGAGTATTTTATTTTATTTTATTTTACTTTTTCCTTTACAGAGGTACTCAAGTTAAAGCCATTGAGTATTCTTTAGCCAAGGCCAT... |
Task1_train_32602 | Here’s a variant located on Chromosome 1. What is the predicted biological effect — harmless or disease-causing? | Benign | CCCCTCCAGGATTACTTACATATACACCATGCGGGGGAGCTCACCACCTCTCAGCCATCCTACTCCCTTATAGGCTGCCCTGACTGGGAGAAAACGTCTGTGTGCTGTGCAAGATCTGCCTCCTGGTCCTGCCCTCTGAGCCTGAAGCCCAGAGGCTTCCAAACTTCTACCCACCCTATCCTGATATTCCAGCAGGATGGAGGGCAGGACAGGGACTGGGAGTGTGTGAAGGGGGCTTGGTGGTGGAGGATAGGCTACGGGTCCTGGAGGGCAGCTTGGGGCATCCAGCCCAACTAACCCCTGCATCGCCTCCTACACAT... | CCCCTCCAGGATTACTTACATATACACCATGCGGGGGAGCTCACCACCTCTCAGCCATCCTACTCCCTTATAGGCTGCCCTGACTGGGAGAAAACGTCTGTGTGCTGTGCAAGATCTGCCTCCTGGTCCTGCCCTCTGAGCCTGAAGCCCAGAGGCTTCCAAACTTCTACCCACCCTATCCTGATATTCCAGCAGGATGGAGGGCAGGACAGGGACTGGGAGTGTGTGAAGGGGGCTTGGTGGTGGAGGATAGGCTACGGGTCCTGGAGGGCAGCTTGGGGCATCCAGCCCAACTAACCCCTGCATCGCCTCCTACACAT... |
Task1_train_32603 | Chromosome 1 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | ACCATGCGGGGGAGCTCACCACCTCTCAGCCATCCTACTCCCTTATAGGCTGCCCTGACTGGGAGAAAACGTCTGTGTGCTGTGCAAGATCTGCCTCCTGGTCCTGCCCTCTGAGCCTGAAGCCCAGAGGCTTCCAAACTTCTACCCACCCTATCCTGATATTCCAGCAGGATGGAGGGCAGGACAGGGACTGGGAGTGTGTGAAGGGGGCTTGGTGGTGGAGGATAGGCTACGGGTCCTGGAGGGCAGCTTGGGGCATCCAGCCCAACTAACCCCTGCATCGCCTCCTACACATTGCCTCCTATCCCTGGACTCCAGGA... | ACCATGCGGGGGAGCTCACCACCTCTCAGCCATCCTACTCCCTTATAGGCTGCCCTGACTGGGAGAAAACGTCTGTGTGCTGTGCAAGATCTGCCTCCTGGTCCTGCCCTCTGAGCCTGAAGCCCAGAGGCTTCCAAACTTCTACCCACCCTATCCTGATATTCCAGCAGGATGGAGGGCAGGACAGGGACTGGGAGTGTGTGAAGGGGGCTTGGTGGTGGAGGATAGGCTACGGGTCCTGGAGGGCAGCTTGGGGCATCCAGCCCAACTAACCCCTGCATCGCCTCCTACACATTGCCTCCTATCCCTGGACTCCAGGA... |
Task1_train_32604 | Given this context: Chromosome 1 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TATTATGCCTTCCCTAACCCAGGATGAAGATGACATCAAACTGTCAGATGCAGACCTCCGGGCTGAAGTGGACACATTCATGTTTGAAGGCCATGACACCACCACCAGTGGTATCTCCTGGTTTCTCTACTGCATGGCCCTGTACCCTGAGCACCAGCATCGTTGTAGAGAGGAGGTCCGCGAGATCCTAGGGGACCAGGACTTCTTCCAGTGGTGAGTCTGAGGGTGGGCCCGGTTTATCCTGCTCAGCCCTTGGGAAGGGCGATGCCCATCCTGTCCTGAACCATCCTGGAAATCAGGTGAGGTGGCGGCTGCTATCC... | TATTATGCCTTCCCTAACCCAGGATGAAGATGACATCAAACTGTCAGATGCAGACCTCCGGGCTGAAGTGGACACATTCATGTTTGAAGGCCATGACACCACCACCAGTGGTATCTCCTGGTTTCTCTACTGCATGGCCCTGTACCCTGAGCACCAGCATCGTTGTAGAGAGGAGGTCCGCGAGATCCTAGGGGACCAGGACTTCTTCCAGTGGTGAGTCTGAGGGTGGGCCCGGTTTATCCTGCTCAGCCCTTGGGAAGGGCGATGCCCATCCTGTCCTGAACCATCCTGGAAATCAGGTGAGGTGGCGGCTGCTATCC... |
Task1_train_32605 | This mutation occurs on Chromosome 1. Does this change lead to a known medical condition, or is it benign? | Benign | CCCGATGGGTGTATTAAGGGAGTCAGAAGGGCAGTGGGAGGCTTCCTGGAGGAGAACTGGGTGGGTGATCCTCAGTGTTGCCCCACCTGCCTCCCACCCCAGGGTCCGGGCTCCTGTCTAACCTCACTCCTCCATCCACCAGCCCCTGTAGCCTTCTAATTCTACTCCAGAAACATCCTTCCTTGCCCTTCCTCAGTATTCTTGCCTGGACTTTATGGTTTTCTGCTTCCCCTCCCAGCACACTGAAGCCACAGCCCAGCTCAGACCCTCCCACGCTCTTCATCACAGGTGGGACAGCATCCCAATGCCTCAGCTGGCAG... | CCCGATGGGTGTATTAAGGGAGTCAGAAGGGCAGTGGGAGGCTTCCTGGAGGAGAACTGGGTGGGTGATCCTCAGTGTTGCCCCACCTGCCTCCCACCCCAGGGTCCGGGCTCCTGTCTAACCTCACTCCTCCATCCACCAGCCCCTGTAGCCTTCTAATTCTACTCCAGAAACATCCTTCCTTGCCCTTCCTCAGTATTCTTGCCTGGACTTTATGGTTTTCTGCTTCCCCTCCCAGCACACTGAAGCCACAGCCCAGCTCAGACCCTCCCACGCTCTTCATCACAGGTGGGACAGCATCCCAATGCCTCAGCTGGCAG... |
Task1_train_32606 | This mutation occurs on Chromosome 1. Does this change lead to a known medical condition, or is it benign? | Benign | ACAGATAAGGACCACAGCTGTGTCCTAACGCAGTGCCTGAGCCACACTGGGCACATAGTATGTGTGCAGTAAGCATGGGCTGAATGAAGGAGCCTACCCCACAGTAGGGCAAGCTGCCTCAGAGCTGGACAATATGATTATCAGAAGGAGGTGGGCAGACATTAGATACTTATGTGGTAGACAGTTGCTTTGAGTTACTAGAAGCAGTTGAAATAAAGAAGAGTTGGCTACATGGAACATCACTAGGACCCAATGTCTTTGAGGGTTCCAGATGAGATTAAAGCAAAGCTGAGTCTTGAAAGCTGAGGAGAGGTGGCTGC... | ACAGATAAGGACCACAGCTGTGTCCTAACGCAGTGCCTGAGCCACACTGGGCACATAGTATGTGTGCAGTAAGCATGGGCTGAATGAAGGAGCCTACCCCACAGTAGGGCAAGCTGCCTCAGAGCTGGACAATATGATTATCAGAAGGAGGTGGGCAGACATTAGATACTTATGTGGTAGACAGTTGCTTTGAGTTACTAGAAGCAGTTGAAATAAAGAAGAGTTGGCTACATGGAACATCACTAGGACCCAATGTCTTTGAGGGTTCCAGATGAGATTAAAGCAAAGCTGAGTCTTGAAAGCTGAGGAGAGGTGGCTGC... |
Task1_train_32607 | This variant is located on Chromosome 1. Evaluate its biological effect and specify any disease association. | Benign | CATAATTCATTGATAAGTGAAAATGAGAATAAGAAACCCAAATCTCAAAATTATAGTCCAACACCAGCACCATATGCATATACTCAGACTCCATCCCATAAATCTGTACATATTCAACATGTAGAATACTATTATGCACACAATTTTATAGTTAATCTTTTTTTGCTTAGCCATACACATCCCAAATGCTATTTTATCTCAACAAATATTTACCATATATTCTGGGACAATATTGAAAATATAACAAGTATGATTATATAAAATTATTGTGTAATTTAAAATGTTCACATTAATTCATTTTATTCTCTAGATATACCAAA... | CATAATTCATTGATAAGTGAAAATGAGAATAAGAAACCCAAATCTCAAAATTATAGTCCAACACCAGCACCATATGCATATACTCAGACTCCATCCCATAAATCTGTACATATTCAACATGTAGAATACTATTATGCACACAATTTTATAGTTAATCTTTTTTTGCTTAGCCATACACATCCCAAATGCTATTTTATCTCAACAAATATTTACCATATATTCTGGGACAATATTGAAAATATAACAAGTATGATTATATAAAATTATTGTGTAATTTAAAATGTTCACATTAATTCATTTTATTCTCTAGATATACCAAA... |
Task1_train_32608 | A mutation is present on Chromosome 1. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TCCTAATGCTGGTGCAAACCTTCCTGAGGCTCAGCTTCTTCCATTTCATGTCTCAGTTCTCTCCAGACATCCTTGGCTTCACATTTATTTTACATCTGCCCACAACCCTTTTCAACCTTTATCTCACAGCTGTCATAATCACATGGATGTAGCAGCTCAATTAGAAAATTCACATGCCTGAAATATACCTCCTTTTCCTGCATTTGCCCATGATGTGGCTTCTTCTGGATAGTTCTTCCCCCAGGAAGCCACCTTTCTCCCTCCCAAATTGTCACCAGTCATCCCTAGGTCCGTGCAGCCTCTGATACACACACATACAC... | TCCTAATGCTGGTGCAAACCTTCCTGAGGCTCAGCTTCTTCCATTTCATGTCTCAGTTCTCTCCAGACATCCTTGGCTTCACATTTATTTTACATCTGCCCACAACCCTTTTCAACCTTTATCTCACAGCTGTCATAATCACATGGATGTAGCAGCTCAATTAGAAAATTCACATGCCTGAAATATACCTCCTTTTCCTGCATTTGCCCATGATGTGGCTTCTTCTGGATAGTTCTTCCCCCAGGAAGCCACCTTTCTCCCTCCCAAATTGTCACCAGTCATCCCTAGGTCCGTGCAGCCTCTGATACACACACATACAC... |
Task1_train_32609 | This variant lies on Chromosome 1. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GGACACACCGCGCCTGCCAGCTGGCCCATCAGCACACAGGTTCTGTCTCTTCCTCTTGTCTCCCAGCCTTTCCCAGGCACAGTGAAAGTACCTGCCCTGACTCCTCAGGCAGAGAAGGTCCCTAGTAATCCTGCAGAAGCCAGAACACACTCAGCCTGGGGAATTCCCTTGCTCAGGGGCTGGGAGCCAAGATGTGAGGGGCCGGATTCTGTGCCTTGGTTTATCAATGTCCCCACATGGAGATAACTGAATGAGACCCTGTCCAAACAGCATTCAAGAGGAGCCTCCATGAACTGTGCCACTGGTGGGAGGGGTGCCCT... | GGACACACCGCGCCTGCCAGCTGGCCCATCAGCACACAGGTTCTGTCTCTTCCTCTTGTCTCCCAGCCTTTCCCAGGCACAGTGAAAGTACCTGCCCTGACTCCTCAGGCAGAGAAGGTCCCTAGTAATCCTGCAGAAGCCAGAACACACTCAGCCTGGGGAATTCCCTTGCTCAGGGGCTGGGAGCCAAGATGTGAGGGGCCGGATTCTGTGCCTTGGTTTATCAATGTCCCCACATGGAGATAACTGAATGAGACCCTGTCCAAACAGCATTCAAGAGGAGCCTCCATGAACTGTGCCACTGGTGGGAGGGGTGCCCT... |
Task1_train_32610 | This variant lies on Chromosome 1. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ACAACAGTGTGTGTCATATCATACATTTTTCTGTCTTGCCCAATGACATTTTTACTTCATTATATAGTGTTCACATATTTACATCTATTTCCCCATTTGGCAAATTCTGTACATGCCTTGAGATCTTTATACCATAGTCCTGTAATCCACTTAGCACAATATTGGCCAAAAACATAAAAATGTGAACAGTACACTGTCTTGGAGAGAAAAGCCCAATAATTATCATATAACGCACAACATTTGAAGCCTCCTGGTATGTGAAATATAAAACACACTTGAAATAGCTATTGAGCTGGAGAGGAAAACTCCAGAATGGCTGC... | ACAACAGTGTGTGTCATATCATACATTTTTCTGTCTTGCCCAATGACATTTTTACTTCATTATATAGTGTTCACATATTTACATCTATTTCCCCATTTGGCAAATTCTGTACATGCCTTGAGATCTTTATACCATAGTCCTGTAATCCACTTAGCACAATATTGGCCAAAAACATAAAAATGTGAACAGTACACTGTCTTGGAGAGAAAAGCCCAATAATTATCATATAACGCACAACATTTGAAGCCTCCTGGTATGTGAAATATAAAACACACTTGAAATAGCTATTGAGCTGGAGAGGAAAACTCCAGAATGGCTGC... |
Task1_train_32611 | This variant lies on Chromosome 1. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ATTAGAAAGTGGAGGCTACGGGGACTGGGATCCACTCCGCCAGAGCTGGCAGAGAATAATCCCGAGGAACCAGCTCCCTCCACACACACACACACACACATTCGCCCCCGCTGGGGAGTGAGGGAGTGTCTGTCTACACTGAGCAAATCCACTGTGAGTCCTCTGCCCGCCCAGCGGATCTTTACTCCCACTCAGACAGAGATGAGAGGTCGCCAAGGGAAGAAGATGGTGCTGGCCCAACCTCCCTGCACAGTCCACCTCGTTCTGCTCAGCTGGACTCTGAAGTGAGGTCGAGTCTCAAAGAGAGGCCTGGCTGAGGT... | ATTAGAAAGTGGAGGCTACGGGGACTGGGATCCACTCCGCCAGAGCTGGCAGAGAATAATCCCGAGGAACCAGCTCCCTCCACACACACACACACACACATTCGCCCCCGCTGGGGAGTGAGGGAGTGTCTGTCTACACTGAGCAAATCCACTGTGAGTCCTCTGCCCGCCCAGCGGATCTTTACTCCCACTCAGACAGAGATGAGAGGTCGCCAAGGGAAGAAGATGGTGCTGGCCCAACCTCCCTGCACAGTCCACCTCGTTCTGCTCAGCTGGACTCTGAAGTGAGGTCGAGTCTCAAAGAGAGGCCTGGCTGAGGT... |
Task1_train_32612 | A mutation is present on Chromosome 1. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | AATGGGGGTCAATGGCTGGGAATTACCTCCTGTCCCCGACCAACCAGTCCAGGGAATCGCAAACAGCTTTCCGCCCCCAACCTGCAGGTGTTTGGAGCCTTTCCTCTACCCCCTCCTCCCCCCACCCGCCTTAAAAAACCCTATACATGACCAATCAGGAATAGCTATTTAGTCCAACAGCAACAACAACCCCTCCCGACAGGCTGTCTGGAACATTTTCGAACCCTCCAACTGGGATCGGTCTGGTTCAGTGTTTGTTTTCTAAGCAGGGAGGTGTCTACGCGGTTGCCTCCTCAGCCAGGTCTCCGGCTGCCGCTACA... | AATGGGGGTCAATGGCTGGGAATTACCTCCTGTCCCCGACCAACCAGTCCAGGGAATCGCAAACAGCTTTCCGCCCCCAACCTGCAGGTGTTTGGAGCCTTTCCTCTACCCCCTCCTCCCCCCACCCGCCTTAAAAAACCCTATACATGACCAATCAGGAATAGCTATTTAGTCCAACAGCAACAACAACCCCTCCCGACAGGCTGTCTGGAACATTTTCGAACCCTCCAACTGGGATCGGTCTGGTTCAGTGTTTGTTTTCTAAGCAGGGAGGTGTCTACGCGGTTGCCTCCTCAGCCAGGTCTCCGGCTGCCGCTACA... |
Task1_train_32613 | This genomic variant is located on Chromosome 1. Can you determine its pathogenicity and name any linked disease? | Benign | ACCTGTAGAATGATGTTCACTTAGGATTGCTTGAAATAACAAATAAGAGATTTGGCCTAAAGGTCCATTAATAGAGCACTGGGGTTCAATATATTCTAGTACAAGGGTACAAAAGAATATTATGCAGCTGTTTAAATACAAGAGAAAGAACTGTATATCCCTATAAGGAAAAGTATCCAAGATATTATAATATCATGTTTAAAACAAAAACAAAAAAACAGGCCAGGTGCAGTGGCTCACGGCTGTAATCCTAGCACTTTGGGAGGCCAAGGTGGGAAGATTGCTTGAGTCTAAGAGTTTGTCTGAGACCAGACTGGGCA... | ACCTGTAGAATGATGTTCACTTAGGATTGCTTGAAATAACAAATAAGAGATTTGGCCTAAAGGTCCATTAATAGAGCACTGGGGTTCAATATATTCTAGTACAAGGGTACAAAAGAATATTATGCAGCTGTTTAAATACAAGAGAAAGAACTGTATATCCCTATAAGGAAAAGTATCCAAGATATTATAATATCATGTTTAAAACAAAAACAAAAAAACAGGCCAGGTGCAGTGGCTCACGGCTGTAATCCTAGCACTTTGGGAGGCCAAGGTGGGAAGATTGCTTGAGTCTAAGAGTTTGTCTGAGACCAGACTGGGCA... |
Task1_train_32614 | This variant is present on Chromosome 1. Is the change likely to result in a pathogenic outcome? | Benign | GGAGGCTGCTGTTAGATGAAACTGCAAAGTGTTCTCAGTACCCTTTCCTAAATGGCCTAGAATATGGCTACACTTATACATCAGTTCTGAGGTAGGTGTTACTAGCCTCATTTTTACAAAGGCAGAAACAAAGCGCAAAGAACCTTGCCCAAGGTGACAGATAGGGTAAGTAGTGAAGGCAGGATTGGAACCCCAGGAGCCTGACTTAAGGTCGCTGCTCTTAACTACTATGCAGACCAGGAAACTGAGGCTCCGAAGCGGGGAAGTCACCTAATGAGGGTCACACAGCCTTGCTACAGCGGAGGCAGCTGGGATTCCGG... | GGAGGCTGCTGTTAGATGAAACTGCAAAGTGTTCTCAGTACCCTTTCCTAAATGGCCTAGAATATGGCTACACTTATACATCAGTTCTGAGGTAGGTGTTACTAGCCTCATTTTTACAAAGGCAGAAACAAAGCGCAAAGAACCTTGCCCAAGGTGACAGATAGGGTAAGTAGTGAAGGCAGGATTGGAACCCCAGGAGCCTGACTTAAGGTCGCTGCTCTTAACTACTATGCAGACCAGGAAACTGAGGCTCCGAAGCGGGGAAGTCACCTAATGAGGGTCACACAGCCTTGCTACAGCGGAGGCAGCTGGGATTCCGG... |
Task1_train_32615 | Chromosome 1 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CTGTGTGTGATTGCATGTGTGAGAGTGTGTGTGTACTGTGCCTGTGTGGGCGTGAGTGCATGTGTGTCAGAGTGTGTGTGTGTGTATGTGTGAGAGAGTGTGTGTACTGTGCCTGTGTGGGCGTGAGTGCATGTGTGTGTCAGAGTGTGTGTAATTGCATGAGTGTGTGTGTACTGTGCCTGTGTGGGTGTGAGTGCATGTGTGTCAGAGTGTGTGTGTGTGTACTGTGCCTGTGTGTGTGATTGCATCTGTGTGTGCATGTGTGAGAGTGTGTGTGTACTGTGCCTGTGTGTGTGTGAGTGTACATGTGAGTGTGCATG... | CTGTGTGTGATTGCATGTGTGAGAGTGTGTGTGTACTGTGCCTGTGTGGGCGTGAGTGCATGTGTGTCAGAGTGTGTGTGTGTGTATGTGTGAGAGAGTGTGTGTACTGTGCCTGTGTGGGCGTGAGTGCATGTGTGTGTCAGAGTGTGTGTAATTGCATGAGTGTGTGTGTACTGTGCCTGTGTGGGTGTGAGTGCATGTGTGTCAGAGTGTGTGTGTGTGTACTGTGCCTGTGTGTGTGATTGCATCTGTGTGTGCATGTGTGAGAGTGTGTGTGTACTGTGCCTGTGTGTGTGTGAGTGTACATGTGAGTGTGCATG... |
Task1_train_32616 | A genomic change on Chromosome 1 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | AAAATACCTCATCATATAATCTACAGCCAGAGAGTAACTCAGCAATTGTGTAGTCCAGCATTTCTACAACCTAGGTATCCACATGTACCTTAGGATGACATTGGCAGGTAGTGTGAGGAGCTAGGGGAATGGGGGGTGGTGGCAAGAATAACAAATAGTGGTACATGCTAAATTTAGTTTAGAAAATTCTGGGTTAATTCGATAAATATTTAAGGAACATCAATTACATGCCAGGCTGTCTACTAGATGCAGAGTAAGACAGATTTATACCAGAATTTTCTTAAAGCCTCGAACAAGCTACTGTTCACAATGAGCACAGT... | AAAATACCTCATCATATAATCTACAGCCAGAGAGTAACTCAGCAATTGTGTAGTCCAGCATTTCTACAACCTAGGTATCCACATGTACCTTAGGATGACATTGGCAGGTAGTGTGAGGAGCTAGGGGAATGGGGGGTGGTGGCAAGAATAACAAATAGTGGTACATGCTAAATTTAGTTTAGAAAATTCTGGGTTAATTCGATAAATATTTAAGGAACATCAATTACATGCCAGGCTGTCTACTAGATGCAGAGTAAGACAGATTTATACCAGAATTTTCTTAAAGCCTCGAACAAGCTACTGTTCACAATGAGCACAGT... |
Task1_train_32617 | Given this context: Chromosome 1 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GGATCACTAAGGTCTCCCTGAGTGTCAGCACCATTTCATTGGTATATGACAATGCAACATGCAAGAAAAAAATGATTAAGGATCAAGATAATTTTATTTAGGCAGAGGACCTGAAAGAGACAATCCCCAAATTAACTTGTAAATGAGATTCTAAGAATTCTTTTGAGTTTTATAAAGCTTTAAACGTTTAAGAACTTTAACCAATCACGAATGACTTCTAAGAATGAACTGAGCATTTTCCTCTAGATGTGAGCTCCTCAGAGGCAGGGGTCATGCTTTAATCAGCCACTCATCCCAGCACTTCCCTCCTGTCAGGGGCC... | GGATCACTAAGGTCTCCCTGAGTGTCAGCACCATTTCATTGGTATATGACAATGCAACATGCAAGAAAAAAATGATTAAGGATCAAGATAATTTTATTTAGGCAGAGGACCTGAAAGAGACAATCCCCAAATTAACTTGTAAATGAGATTCTAAGAATTCTTTTGAGTTTTATAAAGCTTTAAACGTTTAAGAACTTTAACCAATCACGAATGACTTCTAAGAATGAACTGAGCATTTTCCTCTAGATGTGAGCTCCTCAGAGGCAGGGGTCATGCTTTAATCAGCCACTCATCCCAGCACTTCCCTCCTGTCAGGGGCC... |
Task1_train_32618 | Assess the clinical impact of this variant found on Chromosome 1. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | ACTAGCTGATAATAGCATTCTCTTTTCCTATTGAACCCAGATTTGGATTTAGAACGCTTCCTACCAAAATGCTGCAATTAACTGTCACCAACTAGGATAGAGGCTGTACTTGCAATCTCTTTGCTGGCCCTGACCTTTGACTTATAATAAATACTTAGCTGTTTTCTACCTATAAACAGAAAGAGGTCAGTTCACCAGGGTCAACTCACTTGGTTGGAGGATAGAATATTAAAAAGACAATCTTCAGAAATGATACAAGTTACAAATAGACATGGATTTGCACGTCTAAGGATCTACACCATGATATTTTTTGGCTTTTT... | ACTAGCTGATAATAGCATTCTCTTTTCCTATTGAACCCAGATTTGGATTTAGAACGCTTCCTACCAAAATGCTGCAATTAACTGTCACCAACTAGGATAGAGGCTGTACTTGCAATCTCTTTGCTGGCCCTGACCTTTGACTTATAATAAATACTTAGCTGTTTTCTACCTATAAACAGAAAGAGGTCAGTTCACCAGGGTCAACTCACTTGGTTGGAGGATAGAATATTAAAAAGACAATCTTCAGAAATGATACAAGTTACAAATAGACATGGATTTGCACGTCTAAGGATCTACACCATGATATTTTTTGGCTTTTT... |
Task1_train_32619 | This alteration occurs on Chromosome 1. Is it associated with a disease or is it a benign variant? | Benign | TTTGGGAGGCCAAGGCATGCACATTGCAAGATCAAGGGATCGAGACCATCCCGGCCAACATGGTGAAACCCCGTCTCTACTAAAAACACAAAAATTGGCTAGGTGTGGTGGTGCGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCTGAGATTACGCCACTGCACTCCAGCCTGGCGACAGAGCAAGACTCTGTCTTTAAAAAAAAAAAAAAAAAAAAGGAAAGTTAAGTAAGGCTGGGCGCGATGGCTCACACCTGTAATCCCAACACTTTGAG... | TTTGGGAGGCCAAGGCATGCACATTGCAAGATCAAGGGATCGAGACCATCCCGGCCAACATGGTGAAACCCCGTCTCTACTAAAAACACAAAAATTGGCTAGGTGTGGTGGTGCGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCTGAGATTACGCCACTGCACTCCAGCCTGGCGACAGAGCAAGACTCTGTCTTTAAAAAAAAAAAAAAAAAAAAGGAAAGTTAAGTAAGGCTGGGCGCGATGGCTCACACCTGTAATCCCAACACTTTGAG... |
Task1_train_32620 | Chromosome 1 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CCAGCCCATTTCATCCTATCTTTTTTTTTTTTTTTTTGAGATGGAGTCTCCTTCTGTCACCTAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCACGTGCCACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGCTGGTCTTGAACACCTGACCTTGTGATCCACCCGCCTTGGGCTCCTGAAGTGCTGGGGTTACAGGCATGAGCCACCGCACCCAGCCTAA... | CCAGCCCATTTCATCCTATCTTTTTTTTTTTTTTTTTGAGATGGAGTCTCCTTCTGTCACCTAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCACGTGCCACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGCTGGTCTTGAACACCTGACCTTGTGATCCACCCGCCTTGGGCTCCTGAAGTGCTGGGGTTACAGGCATGAGCCACCGCACCCAGCCTAA... |
Task1_train_32621 | Consider a variant on Chromosome 1. Determine its clinical classification and disease relevance. | Benign | GAAGCATAGCCCAGTTCTTCTTGCCTTCATGAATTCAAGCTCGCTTACCTCATCCTGGAAAATATCTGTCTCCTCTGAATTTATTTTTCTACTCCTACATAATAGTTTTCAGACACTGAGTCCTCACTTGATGTCTTTGATAAGTTCTTGGAAACTGTGACTTTAAGCAAATTGATACACTGTATGCCGGAGAACCTTAACTGTTGTTTATATCAATTAGCTTATAGTAAAATTGGCTTCTTTATACAGTGAGTTGTTTTGCTTATAATTGCAGTTTCCAAGAACCTATCAACAATGTTAAGTGAGGACTTACTGTACCT... | GAAGCATAGCCCAGTTCTTCTTGCCTTCATGAATTCAAGCTCGCTTACCTCATCCTGGAAAATATCTGTCTCCTCTGAATTTATTTTTCTACTCCTACATAATAGTTTTCAGACACTGAGTCCTCACTTGATGTCTTTGATAAGTTCTTGGAAACTGTGACTTTAAGCAAATTGATACACTGTATGCCGGAGAACCTTAACTGTTGTTTATATCAATTAGCTTATAGTAAAATTGGCTTCTTTATACAGTGAGTTGTTTTGCTTATAATTGCAGTTTCCAAGAACCTATCAACAATGTTAAGTGAGGACTTACTGTACCT... |
Task1_train_32622 | A mutation has occurred on Chromosome 1. What is the medical relevance of this mutation? | Benign | GCCTAAAAGCCTTAAGGCAGGAAGCAAAGGCTCACTGGAGAGGCCAGAGGCCATGGCAGAGGCAAATACAGAGCCCCACTTGGTGGAAGCCAGGATATGGCTCCCGGGGGGTAGTCTAGGAGAACAGAGAGGCCTTTGAGGCTGGCTGCCACGGAGGAGTTTCTTGTGCTCAGTTTCTGCTTGGGGCGGCTGCTGGGGGAGGGTCCTGGAAAGGGTGACTGCAGCCTTGCTGTGCAGGCCAGGCCACACACGTGTTACGTCTGGGCGCACAGGAGCATCAGAGGCACAGGGGCCCTCCTCCAGAACCCACCTGAGCTGCT... | GCCTAAAAGCCTTAAGGCAGGAAGCAAAGGCTCACTGGAGAGGCCAGAGGCCATGGCAGAGGCAAATACAGAGCCCCACTTGGTGGAAGCCAGGATATGGCTCCCGGGGGGTAGTCTAGGAGAACAGAGAGGCCTTTGAGGCTGGCTGCCACGGAGGAGTTTCTTGTGCTCAGTTTCTGCTTGGGGCGGCTGCTGGGGGAGGGTCCTGGAAAGGGTGACTGCAGCCTTGCTGTGCAGGCCAGGCCACACACGTGTTACGTCTGGGCGCACAGGAGCATCAGAGGCACAGGGGCCCTCCTCCAGAACCCACCTGAGCTGCT... |
Task1_train_32623 | Chromosome 1 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AATTTAAAAAAAAAAGACTTCAGTAGGTTAAATAATTTTCATATATGCTAAAAAAATTTATTTTGTTTTACAGATAAGATTCAAAATTCATACCTGGATGTCTCTTAAGAATTTTTGCCAAATTTTCAATTATTTCCTTACAATTTAATTTCTAAAAAACAAATCAAATAAATAAGTTTGACTCAATTTCACCTTGTGCAAATTCTACTTTAATCTAAGCATTTAATAGTAGCATTTACAATTTCCAGCCATAAAGCTCTATAATAACCTTGCTACTCCAAGTAAGTGATTCATAGACCTACAGTATCAGCATAATCTGG... | AATTTAAAAAAAAAAGACTTCAGTAGGTTAAATAATTTTCATATATGCTAAAAAAATTTATTTTGTTTTACAGATAAGATTCAAAATTCATACCTGGATGTCTCTTAAGAATTTTTGCCAAATTTTCAATTATTTCCTTACAATTTAATTTCTAAAAAACAAATCAAATAAATAAGTTTGACTCAATTTCACCTTGTGCAAATTCTACTTTAATCTAAGCATTTAATAGTAGCATTTACAATTTCCAGCCATAAAGCTCTATAATAACCTTGCTACTCCAAGTAAGTGATTCATAGACCTACAGTATCAGCATAATCTGG... |
Task1_train_32624 | Chromosome 1 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GGATAGAGTGTAGAAGGTTCATGAATTTACGTGGGAAAAATCACATCCTTGGTATGCATTACCTCTAACTGAAATTCAGTATTTTCTTTCATCATGCATATTGGTAAGAAAACCCACGATAGTATTAGTAGTGCTTGTGACTTTGTCACCAATAGAAATCACAGATATTTTCATATTGTATTACAGTAGAGACATATTGAAATACTAGTTATTTTCATTCACCACTTCAAAATTATAGTAATTAATAGACTCATCTCTAGATCTTATTGACACTTTTTAAAAAGTAGGACAAATCATGATTCAATATAATTGGTATCCTC... | GGATAGAGTGTAGAAGGTTCATGAATTTACGTGGGAAAAATCACATCCTTGGTATGCATTACCTCTAACTGAAATTCAGTATTTTCTTTCATCATGCATATTGGTAAGAAAACCCACGATAGTATTAGTAGTGCTTGTGACTTTGTCACCAATAGAAATCACAGATATTTTCATATTGTATTACAGTAGAGACATATTGAAATACTAGTTATTTTCATTCACCACTTCAAAATTATAGTAATTAATAGACTCATCTCTAGATCTTATTGACACTTTTTAAAAAGTAGGACAAATCATGATTCAATATAATTGGTATCCTC... |
Task1_train_32625 | A genomic variant on Chromosome 1 is under review. What is the biological outcome — benign or pathogenic? | Benign | TGCATTACCTCTAACTGAAATTCAGTATTTTCTTTCATCATGCATATTGGTAAGAAAACCCACGATAGTATTAGTAGTGCTTGTGACTTTGTCACCAATAGAAATCACAGATATTTTCATATTGTATTACAGTAGAGACATATTGAAATACTAGTTATTTTCATTCACCACTTCAAAATTATAGTAATTAATAGACTCATCTCTAGATCTTATTGACACTTTTTAAAAAGTAGGACAAATCATGATTCAATATAATTGGTATCCTCTGTAACCCTAAATAATTTTTTTTTTTAGTTAAAAACATTATTTGTGGCCTGGTG... | TGCATTACCTCTAACTGAAATTCAGTATTTTCTTTCATCATGCATATTGGTAAGAAAACCCACGATAGTATTAGTAGTGCTTGTGACTTTGTCACCAATAGAAATCACAGATATTTTCATATTGTATTACAGTAGAGACATATTGAAATACTAGTTATTTTCATTCACCACTTCAAAATTATAGTAATTAATAGACTCATCTCTAGATCTTATTGACACTTTTTAAAAAGTAGGACAAATCATGATTCAATATAATTGGTATCCTCTGTAACCCTAAATAATTTTTTTTTTTAGTTAAAAACATTATTTGTGGCCTGGTG... |
Task1_train_32626 | Here’s a variant located on Chromosome 1. What is the predicted biological effect — harmless or disease-causing? | Benign | TAGAAATCACAGATATTTTCATATTGTATTACAGTAGAGACATATTGAAATACTAGTTATTTTCATTCACCACTTCAAAATTATAGTAATTAATAGACTCATCTCTAGATCTTATTGACACTTTTTAAAAAGTAGGACAAATCATGATTCAATATAATTGGTATCCTCTGTAACCCTAAATAATTTTTTTTTTTAGTTAAAAACATTATTTGTGGCCTGGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGTGGATCACTTGAGGTCAGGAGTTCAAGACCAGCCTGGGCAACATGGTGAAA... | TAGAAATCACAGATATTTTCATATTGTATTACAGTAGAGACATATTGAAATACTAGTTATTTTCATTCACCACTTCAAAATTATAGTAATTAATAGACTCATCTCTAGATCTTATTGACACTTTTTAAAAAGTAGGACAAATCATGATTCAATATAATTGGTATCCTCTGTAACCCTAAATAATTTTTTTTTTTAGTTAAAAACATTATTTGTGGCCTGGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGTGGATCACTTGAGGTCAGGAGTTCAAGACCAGCCTGGGCAACATGGTGAAA... |
Task1_train_32627 | 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 | CACACACACACACACACACACACACAATTAGTCCTCATATTCTCCAATTCTGTATTTGCAAATTTCCCTACTTGCTAAAATTTACTTGTAACGTCAGCATCAATACTCAAGGCAATTCTGAGGTCATTTGTAAATGTGGGCACACACAGAGTAGCAAAAAATTTGATTTACACATGTATCCTAGGTGATATTGAATAAGGTATGCTCTGCCTTCTCTTTGCAGCTCTCATGGTACAAGCAAGTGTCTTTTTCTCAGTCTATTTAGTGCCATGGTTTTTGTATTTTTTTATTTTTAATGGGTGATTTCACTGTTTTGTTTT... | CACACACACACACACACACACACACAATTAGTCCTCATATTCTCCAATTCTGTATTTGCAAATTTCCCTACTTGCTAAAATTTACTTGTAACGTCAGCATCAATACTCAAGGCAATTCTGAGGTCATTTGTAAATGTGGGCACACACAGAGTAGCAAAAAATTTGATTTACACATGTATCCTAGGTGATATTGAATAAGGTATGCTCTGCCTTCTCTTTGCAGCTCTCATGGTACAAGCAAGTGTCTTTTTCTCAGTCTATTTAGTGCCATGGTTTTTGTATTTTTTTATTTTTAATGGGTGATTTCACTGTTTTGTTTT... |
Task1_train_32628 | Given this variant on Chromosome 1, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | ACACACACACAATTAGTCCTCATATTCTCCAATTCTGTATTTGCAAATTTCCCTACTTGCTAAAATTTACTTGTAACGTCAGCATCAATACTCAAGGCAATTCTGAGGTCATTTGTAAATGTGGGCACACACAGAGTAGCAAAAAATTTGATTTACACATGTATCCTAGGTGATATTGAATAAGGTATGCTCTGCCTTCTCTTTGCAGCTCTCATGGTACAAGCAAGTGTCTTTTTCTCAGTCTATTTAGTGCCATGGTTTTTGTATTTTTTTATTTTTAATGGGTGATTTCACTGTTTTGTTTTGGTTTATTTTTATTT... | ACACACACACAATTAGTCCTCATATTCTCCAATTCTGTATTTGCAAATTTCCCTACTTGCTAAAATTTACTTGTAACGTCAGCATCAATACTCAAGGCAATTCTGAGGTCATTTGTAAATGTGGGCACACACAGAGTAGCAAAAAATTTGATTTACACATGTATCCTAGGTGATATTGAATAAGGTATGCTCTGCCTTCTCTTTGCAGCTCTCATGGTACAAGCAAGTGTCTTTTTCTCAGTCTATTTAGTGCCATGGTTTTTGTATTTTTTTATTTTTAATGGGTGATTTCACTGTTTTGTTTTGGTTTATTTTTATTT... |
Task1_train_32629 | Consider this mutation on Chromosome 1. Is this a benign change or a disease-causing variant? | Benign | ATATTCTCCAATTCTGTATTTGCAAATTTCCCTACTTGCTAAAATTTACTTGTAACGTCAGCATCAATACTCAAGGCAATTCTGAGGTCATTTGTAAATGTGGGCACACACAGAGTAGCAAAAAATTTGATTTACACATGTATCCTAGGTGATATTGAATAAGGTATGCTCTGCCTTCTCTTTGCAGCTCTCATGGTACAAGCAAGTGTCTTTTTCTCAGTCTATTTAGTGCCATGGTTTTTGTATTTTTTTATTTTTAATGGGTGATTTCACTGTTTTGTTTTGGTTTATTTTTATTTTCATTTTTTGAGATGGAGTCT... | ATATTCTCCAATTCTGTATTTGCAAATTTCCCTACTTGCTAAAATTTACTTGTAACGTCAGCATCAATACTCAAGGCAATTCTGAGGTCATTTGTAAATGTGGGCACACACAGAGTAGCAAAAAATTTGATTTACACATGTATCCTAGGTGATATTGAATAAGGTATGCTCTGCCTTCTCTTTGCAGCTCTCATGGTACAAGCAAGTGTCTTTTTCTCAGTCTATTTAGTGCCATGGTTTTTGTATTTTTTTATTTTTAATGGGTGATTTCACTGTTTTGTTTTGGTTTATTTTTATTTTCATTTTTTGAGATGGAGTCT... |
Task1_train_32630 | A variant was discovered on Chromosome 1. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CCCACCACCACACCCAGATAATTTTTGTATTTTTAGTAGATACGAGGTTTCACTATGTTGGCCAGGCTGTTCTCGAAATCCTGACCTCGTGATCCGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTGCAAGCGTGAGCCACTGCACCTGGCCTAGTTTTGTTTTTGTTTTTGAGACAGAGTCTTGCTGTGTTGCCCAGGCTGGAGTGCAGTGGCACAGTCTCAGTTTACTGCAACCTCTGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCGAAGTAGCTGGGATTACAGGTATGCATCACCACGCCCAGCTAA... | CCCACCACCACACCCAGATAATTTTTGTATTTTTAGTAGATACGAGGTTTCACTATGTTGGCCAGGCTGTTCTCGAAATCCTGACCTCGTGATCCGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTGCAAGCGTGAGCCACTGCACCTGGCCTAGTTTTGTTTTTGTTTTTGAGACAGAGTCTTGCTGTGTTGCCCAGGCTGGAGTGCAGTGGCACAGTCTCAGTTTACTGCAACCTCTGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCGAAGTAGCTGGGATTACAGGTATGCATCACCACGCCCAGCTAA... |
Task1_train_32631 | A sequence alteration has been identified on Chromosome 1. Is it disease-inducing or harmless? | Benign | TAGGTGCACTCTGTGATGCTCCCACAATGACCACAATCACCTAATGATGCATTTCTCAGAATGTAGCCCCGTTGTTAAGCAACACATGACTCTATGAGAAATAAAGCCGCTAAGAACAGTGAAGAATGGTTTACCACCCAACCTCAAGCTCAAAGGCAGCAGGTAAAATGTAACAGTGCTCTTGTGCCATCAGCCCCAGTGGAAGGCAGAACCTGCAGCTTCTAATATGAACATCAAATGACCCCAACTCATTCCCTGTGAGGGCTCCGTGTGTGATCTCATCCCCATGCCTCCTCTGCACTGTCATCTTGGTTTCTGTC... | TAGGTGCACTCTGTGATGCTCCCACAATGACCACAATCACCTAATGATGCATTTCTCAGAATGTAGCCCCGTTGTTAAGCAACACATGACTCTATGAGAAATAAAGCCGCTAAGAACAGTGAAGAATGGTTTACCACCCAACCTCAAGCTCAAAGGCAGCAGGTAAAATGTAACAGTGCTCTTGTGCCATCAGCCCCAGTGGAAGGCAGAACCTGCAGCTTCTAATATGAACATCAAATGACCCCAACTCATTCCCTGTGAGGGCTCCGTGTGTGATCTCATCCCCATGCCTCCTCTGCACTGTCATCTTGGTTTCTGTC... |
Task1_train_32632 | Given a variant located on Chromosome 1, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CGGAGCAGTAAAGTGGCTCATCCAGGCTTACACAGCAGTCAGAATTGGAACCCATGCCCTTCTGTCTCTAAAGCTCTCCATATGAGAAACACTCACTGCTGGCTGAGCTTCCCCGCTGTCCAGGGGTTTGAGATGTTCCTCACCAGGTGGACTTGAAACTCCTGGAGACCAGGGAGCTCCCCTGTTCTTCCCCACACACCTCCCACATGGCTGGGTACACAGAAGGGGCCTTGGGGGGCTTATCTTGCTCCATTCTTAGAAGAGCAAGGCTGGGTACAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC... | CGGAGCAGTAAAGTGGCTCATCCAGGCTTACACAGCAGTCAGAATTGGAACCCATGCCCTTCTGTCTCTAAAGCTCTCCATATGAGAAACACTCACTGCTGGCTGAGCTTCCCCGCTGTCCAGGGGTTTGAGATGTTCCTCACCAGGTGGACTTGAAACTCCTGGAGACCAGGGAGCTCCCCTGTTCTTCCCCACACACCTCCCACATGGCTGGGTACACAGAAGGGGCCTTGGGGGGCTTATCTTGCTCCATTCTTAGAAGAGCAAGGCTGGGTACAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC... |
Task1_train_32633 | A variant on Chromosome 1 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | ATTTAAAAATTTGGCTGGCACGGTTGTGACCCCCTATAGTCCCAGTTGCTTGAGAGGCTGAGGCTGGAGGATCACTTCAGCCCCGGAGCTCAAGGTTACAGTGAGCTATGATTGCACCACTGCACTCCAGCCTGGGTGACAGAGTGAGGCCTTGTCTTAAAAAAAAAAAAAAAAAAAAGCCCAGCAAGATCTACAAGATCTAGACAAGGGAAGGAAAAGGAGCAGCAGCAGAGGATTCTGGAGTGAGCAGTGGTGTGGCAGGGGTGCAGACCATGCCCATGGAACAGACAATTAGTGGCAGGAAAAGCTAACGTTTACTG... | ATTTAAAAATTTGGCTGGCACGGTTGTGACCCCCTATAGTCCCAGTTGCTTGAGAGGCTGAGGCTGGAGGATCACTTCAGCCCCGGAGCTCAAGGTTACAGTGAGCTATGATTGCACCACTGCACTCCAGCCTGGGTGACAGAGTGAGGCCTTGTCTTAAAAAAAAAAAAAAAAAAAAGCCCAGCAAGATCTACAAGATCTAGACAAGGGAAGGAAAAGGAGCAGCAGCAGAGGATTCTGGAGTGAGCAGTGGTGTGGCAGGGGTGCAGACCATGCCCATGGAACAGACAATTAGTGGCAGGAAAAGCTAACGTTTACTG... |
Task1_train_32634 | Mutation context: Chromosome 1. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GGTTGTGACCCCCTATAGTCCCAGTTGCTTGAGAGGCTGAGGCTGGAGGATCACTTCAGCCCCGGAGCTCAAGGTTACAGTGAGCTATGATTGCACCACTGCACTCCAGCCTGGGTGACAGAGTGAGGCCTTGTCTTAAAAAAAAAAAAAAAAAAAAGCCCAGCAAGATCTACAAGATCTAGACAAGGGAAGGAAAAGGAGCAGCAGCAGAGGATTCTGGAGTGAGCAGTGGTGTGGCAGGGGTGCAGACCATGCCCATGGAACAGACAATTAGTGGCAGGAAAAGCTAACGTTTACTGAGCACTTACTATGTGCAGTAC... | GGTTGTGACCCCCTATAGTCCCAGTTGCTTGAGAGGCTGAGGCTGGAGGATCACTTCAGCCCCGGAGCTCAAGGTTACAGTGAGCTATGATTGCACCACTGCACTCCAGCCTGGGTGACAGAGTGAGGCCTTGTCTTAAAAAAAAAAAAAAAAAAAAGCCCAGCAAGATCTACAAGATCTAGACAAGGGAAGGAAAAGGAGCAGCAGCAGAGGATTCTGGAGTGAGCAGTGGTGTGGCAGGGGTGCAGACCATGCCCATGGAACAGACAATTAGTGGCAGGAAAAGCTAACGTTTACTGAGCACTTACTATGTGCAGTAC... |
Task1_train_32635 | This sequence change occurs on Chromosome 1. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GTCAGGCAAGGACTCCAGGGCTGAAAGGGTCAGGGGTCAACTGAGACCTTGAAAGGCGTGGAGGGGCCTCTGCCAGGGGTCAGGAAATCCTATTTCTCCCGCTAGCTTATGGGACCACCTGTGGTGGGGCACGGCCCCTTCTGGTCCTTGGTTCTGTCAGCTGTGTAGGCAACATCTGAGGTGCTTCTAACTCTGTACCCTTGAGTTTGGATGGAAGGAGAGCAGCCTGGGCAAGGGTTTAGAGGCTCACCAGTTGAGCTGGCGCAGGGCCTGGGGAGCCCAGGTGGGTGAGGACCTGTGCCTTGACCCCCAGGTCTGTG... | GTCAGGCAAGGACTCCAGGGCTGAAAGGGTCAGGGGTCAACTGAGACCTTGAAAGGCGTGGAGGGGCCTCTGCCAGGGGTCAGGAAATCCTATTTCTCCCGCTAGCTTATGGGACCACCTGTGGTGGGGCACGGCCCCTTCTGGTCCTTGGTTCTGTCAGCTGTGTAGGCAACATCTGAGGTGCTTCTAACTCTGTACCCTTGAGTTTGGATGGAAGGAGAGCAGCCTGGGCAAGGGTTTAGAGGCTCACCAGTTGAGCTGGCGCAGGGCCTGGGGAGCCCAGGTGGGTGAGGACCTGTGCCTTGACCCCCAGGTCTGTG... |
Task1_train_32636 | Consider this mutation on Chromosome 1. Is this a benign change or a disease-causing variant? | Benign | AGGTGGTACCCAGCTCTGAGCTAAGAAGAGCCTCTGATGGGCAGAGCTGCCCCACTGTGGGTTGAGATGCTCGGGAAGTGGTGACCTCCCTGCTGCTGGAGGTGTGTAAGGATGCTCCTGCCAAGTCCACTAAAGAGCAGACTCCTGCCTTGTGCTGGGACAGACTCGATTGCTCAAGGGGTCTTAGAGATGTGACACCTAGAAGGGGCTGCTAAGCTTGTCTGCATGAAGGTGGGATGACCGATTGCATGACATCTGACCTCTCCCAGGTGAGGAGGCCTCAGGGAAGGAAGGATGCTCTCGTGGAGGCCTGCAGCCCC... | AGGTGGTACCCAGCTCTGAGCTAAGAAGAGCCTCTGATGGGCAGAGCTGCCCCACTGTGGGTTGAGATGCTCGGGAAGTGGTGACCTCCCTGCTGCTGGAGGTGTGTAAGGATGCTCCTGCCAAGTCCACTAAAGAGCAGACTCCTGCCTTGTGCTGGGACAGACTCGATTGCTCAAGGGGTCTTAGAGATGTGACACCTAGAAGGGGCTGCTAAGCTTGTCTGCATGAAGGTGGGATGACCGATTGCATGACATCTGACCTCTCCCAGGTGAGGAGGCCTCAGGGAAGGAAGGATGCTCTCGTGGAGGCCTGCAGCCCC... |
Task1_train_32637 | This alteration on Chromosome 1 may affect genome function. Does it lead to a disease or is it benign? | Benign | GCAAGTGGAGTGTTACCATATTTTATTCCTTTAAACCAAGAAAGGAAACAGAAGAGGAAGAAAAAGCAATTAATAAACATTAGGAAAATGCAAACCAAATCTGCAATGCTATACTACTTTACACCTACCAGAATATCTCCACGCCACAAGACATGTAACAAGTGCTGCTGAGGATGTGGAAAAATTGGAACCCTCACAGACAGCTCGTGGGAATGGTGCAGCCACTTTGGAAAACATCCTGGCAGTTCCTCAAAGGTTAAACAGAGACTTACCATGTGATAGTAGTTCCACTCCTAGCTATGTCCATACAAAAACATGTA... | GCAAGTGGAGTGTTACCATATTTTATTCCTTTAAACCAAGAAAGGAAACAGAAGAGGAAGAAAAAGCAATTAATAAACATTAGGAAAATGCAAACCAAATCTGCAATGCTATACTACTTTACACCTACCAGAATATCTCCACGCCACAAGACATGTAACAAGTGCTGCTGAGGATGTGGAAAAATTGGAACCCTCACAGACAGCTCGTGGGAATGGTGCAGCCACTTTGGAAAACATCCTGGCAGTTCCTCAAAGGTTAAACAGAGACTTACCATGTGATAGTAGTTCCACTCCTAGCTATGTCCATACAAAAACATGTA... |
Task1_train_32638 | A mutation found on Chromosome 1 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CTTGCCTCCTAAGCAGGGGTGGGGAAATGCATGTGTCTTTGTCCTCATTTAAGGTCACTTTCAGCTGTGACGCATTAATTCTTTTTTCTTTCTTTTTTTTTTTTTTTTTTGGAGACAAGAGTTTCCCTCCGTCCAGGCTGGAGTGCAATGGCGTGATCTCGGCTCACTGCAACCTCCACCCCCAGGTTCAAGTGATTCTCCTGCCTCTGCCTCCCAAGTAGCTGGGATAATAGGCACCCGCCACTACACCTGGCTAGTTTTTGCATTTTTAGTAAAGAAGGGGTTTTGCCATTTTGGCCAGGCTGGTCTTGAACTCCTGA... | CTTGCCTCCTAAGCAGGGGTGGGGAAATGCATGTGTCTTTGTCCTCATTTAAGGTCACTTTCAGCTGTGACGCATTAATTCTTTTTTCTTTCTTTTTTTTTTTTTTTTTTGGAGACAAGAGTTTCCCTCCGTCCAGGCTGGAGTGCAATGGCGTGATCTCGGCTCACTGCAACCTCCACCCCCAGGTTCAAGTGATTCTCCTGCCTCTGCCTCCCAAGTAGCTGGGATAATAGGCACCCGCCACTACACCTGGCTAGTTTTTGCATTTTTAGTAAAGAAGGGGTTTTGCCATTTTGGCCAGGCTGGTCTTGAACTCCTGA... |
Task1_train_32639 | This sequence variant lies on Chromosome 1. Is it clinically significant, and what condition might it cause if any? | Benign | TGCATGTCATGAGGAGATTGCTGGATTATGCAAAACACACTGCCCAAGCTCCAGAATATAGTTATTTTCTTAGAGTTTAGGAGGCCAAGAGTGACACAGAGGAAGGTCCTAGGTACAGGATGCTAGAACTCCAGAATGTCTGACTGAAAATTCAAAGGGTATCAAGCTGGTGAGACATCCAACTTCATTGAGTTGGGGGCATCTGGCAGGTAGGGATGGGAAGGCATTTGCTTAAGTGTGTCAAGTTCCAGGTATGATGAGATTAGATGCAGCTCCTCTGCTCCTACTTAAGTCAAACACTTCCATGTTGCACCTTGTCC... | TGCATGTCATGAGGAGATTGCTGGATTATGCAAAACACACTGCCCAAGCTCCAGAATATAGTTATTTTCTTAGAGTTTAGGAGGCCAAGAGTGACACAGAGGAAGGTCCTAGGTACAGGATGCTAGAACTCCAGAATGTCTGACTGAAAATTCAAAGGGTATCAAGCTGGTGAGACATCCAACTTCATTGAGTTGGGGGCATCTGGCAGGTAGGGATGGGAAGGCATTTGCTTAAGTGTGTCAAGTTCCAGGTATGATGAGATTAGATGCAGCTCCTCTGCTCCTACTTAAGTCAAACACTTCCATGTTGCACCTTGTCC... |
Task1_train_32640 | A mutation has occurred on Chromosome 1. What is the medical relevance of this mutation? | Benign | TCACTCAACTTCTCTGAGGAGGCATCCTTATCTAGAAAGTAGAATGACAAGAAAATTTCTGCTTTTCACAGCCATCCTCACAAGGACAGTTGTTATAAAGAGCCAGGGAGATAAGGCATAACCAGCCCAGACACGCAGTTTCTATTCCTTGCCTCGTCCTCAGTACTCCCACTCTAAGGAGACCACAGAACAACTCCCAGTGAGGAAACTCACTGCAATATTTTACCAAGGCACAGCCATTTTCATAACCTCAACAGCACTGGGAAATGGTCCAGGGTCATGATTAGACTAAGAACTCTAGAGTTAGATGCTTAAGTTCA... | TCACTCAACTTCTCTGAGGAGGCATCCTTATCTAGAAAGTAGAATGACAAGAAAATTTCTGCTTTTCACAGCCATCCTCACAAGGACAGTTGTTATAAAGAGCCAGGGAGATAAGGCATAACCAGCCCAGACACGCAGTTTCTATTCCTTGCCTCGTCCTCAGTACTCCCACTCTAAGGAGACCACAGAACAACTCCCAGTGAGGAAACTCACTGCAATATTTTACCAAGGCACAGCCATTTTCATAACCTCAACAGCACTGGGAAATGGTCCAGGGTCATGATTAGACTAAGAACTCTAGAGTTAGATGCTTAAGTTCA... |
Task1_train_32641 | Assess the clinical impact of this variant found on Chromosome 1. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GATGCCGTGATTCCACACAGAGGCCCCACTGTGAGAAGACCACTAACCACAGGCAGAAGCCAGGTGTAAGCCAGTGTCCTGTGGAGTCTTGTCAAGGTTCCTTCGGGTCACAGAGCCTCCACCTCGGCCCCCACAGGCACCCACAGACTCACCCATAAAAGAGAATATGTGAAGGAGAACTGTGGCTCAGCAGCTGTCAGCTCCAGGGTCTCGGGGAGATATGGGGGCCCAGCTGTCTCCCAGCAGCCCTGGCCTGGCCTGCGCGCTGTCTATTGGTCAACTCCTAGGCAGGGGCATGTGTCACAGGACCCCAAACAAGC... | GATGCCGTGATTCCACACAGAGGCCCCACTGTGAGAAGACCACTAACCACAGGCAGAAGCCAGGTGTAAGCCAGTGTCCTGTGGAGTCTTGTCAAGGTTCCTTCGGGTCACAGAGCCTCCACCTCGGCCCCCACAGGCACCCACAGACTCACCCATAAAAGAGAATATGTGAAGGAGAACTGTGGCTCAGCAGCTGTCAGCTCCAGGGTCTCGGGGAGATATGGGGGCCCAGCTGTCTCCCAGCAGCCCTGGCCTGGCCTGCGCGCTGTCTATTGGTCAACTCCTAGGCAGGGGCATGTGTCACAGGACCCCAAACAAGC... |
Task1_train_32642 | Here is a mutation located on Chromosome 1. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CTGTCTCCCAGCAGCCCTGGCCTGGCCTGCGCGCTGTCTATTGGTCAACTCCTAGGCAGGGGCATGTGTCACAGGACCCCAAACAAGCCAGAGCATCGCCAGGGGCTGGCCCAGCCACCAGGCCTCCTTCCAGCATCCTCTCAGCCCAAAGGCACAAGATAAAGTCAAAGTCTCAGCCTGTCCAATGCACTCTCCCCACCACTGCTCCACACACCAGAATGCTAACCACAAGCTCCCTCCTCCTGCCTCCCCTTGGCACAGGCCATTCACTGCTGCTCACTTGTTTACAAAGCAAACTCTTTCTCCTCCTTCAAGACCCA... | CTGTCTCCCAGCAGCCCTGGCCTGGCCTGCGCGCTGTCTATTGGTCAACTCCTAGGCAGGGGCATGTGTCACAGGACCCCAAACAAGCCAGAGCATCGCCAGGGGCTGGCCCAGCCACCAGGCCTCCTTCCAGCATCCTCTCAGCCCAAAGGCACAAGATAAAGTCAAAGTCTCAGCCTGTCCAATGCACTCTCCCCACCACTGCTCCACACACCAGAATGCTAACCACAAGCTCCCTCCTCCTGCCTCCCCTTGGCACAGGCCATTCACTGCTGCTCACTTGTTTACAAAGCAAACTCTTTCTCCTCCTTCAAGACCCA... |
Task1_train_32643 | A variant affecting Chromosome 1 has been observed. Determine if it's benign or associated with disease. | Benign | AAACAATGCACGGCTCAAAAACTATAAGACGCTTGCTCCTTGCTATGGACTGATTTGTGTCCCCCCAAAATTTATACATTGAAGCCCTAACATCCAGTTTGACTGTGTTTGGAGACAGAGCCTTTAAATAAATAATTAAGGCTAAACAAGGTTATAAGGTTGAGGGCCTACTCTGATAGGACAGGTGTTCTTATAAGAAATGAGGGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGTGAATTGCTTGAGCCCAGGAGTTCAAGACCAGCCCGGCCAACATGGTGAAACCCCGTCTC... | AAACAATGCACGGCTCAAAAACTATAAGACGCTTGCTCCTTGCTATGGACTGATTTGTGTCCCCCCAAAATTTATACATTGAAGCCCTAACATCCAGTTTGACTGTGTTTGGAGACAGAGCCTTTAAATAAATAATTAAGGCTAAACAAGGTTATAAGGTTGAGGGCCTACTCTGATAGGACAGGTGTTCTTATAAGAAATGAGGGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGTGAATTGCTTGAGCCCAGGAGTTCAAGACCAGCCCGGCCAACATGGTGAAACCCCGTCTC... |
Task1_train_32644 | Given this variant on Chromosome 1, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TTTGTGTCCCCCCAAAATTTATACATTGAAGCCCTAACATCCAGTTTGACTGTGTTTGGAGACAGAGCCTTTAAATAAATAATTAAGGCTAAACAAGGTTATAAGGTTGAGGGCCTACTCTGATAGGACAGGTGTTCTTATAAGAAATGAGGGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGTGAATTGCTTGAGCCCAGGAGTTCAAGACCAGCCCGGCCAACATGGTGAAACCCCGTCTCTATAAAAAATTAGCCAGGCGTGGTGGCACACGCCTGTAGTCTCAGCTGCTGGA... | TTTGTGTCCCCCCAAAATTTATACATTGAAGCCCTAACATCCAGTTTGACTGTGTTTGGAGACAGAGCCTTTAAATAAATAATTAAGGCTAAACAAGGTTATAAGGTTGAGGGCCTACTCTGATAGGACAGGTGTTCTTATAAGAAATGAGGGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGTGAATTGCTTGAGCCCAGGAGTTCAAGACCAGCCCGGCCAACATGGTGAAACCCCGTCTCTATAAAAAATTAGCCAGGCGTGGTGGCACACGCCTGTAGTCTCAGCTGCTGGA... |
Task1_train_32645 | Chromosome 1 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CAAGGTTATAAGGTTGAGGGCCTACTCTGATAGGACAGGTGTTCTTATAAGAAATGAGGGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGTGAATTGCTTGAGCCCAGGAGTTCAAGACCAGCCCGGCCAACATGGTGAAACCCCGTCTCTATAAAAAATTAGCCAGGCGTGGTGGCACACGCCTGTAGTCTCAGCTGCTGGAGTGGCTGAGGTGGCAGGATCACTTGAGCCTGGGAGGTGGAGGCTGCAGCGAGCCAACATTGTGCCACTGCACTCCAGCCTGGGTGACAGAGTC... | CAAGGTTATAAGGTTGAGGGCCTACTCTGATAGGACAGGTGTTCTTATAAGAAATGAGGGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGTGAATTGCTTGAGCCCAGGAGTTCAAGACCAGCCCGGCCAACATGGTGAAACCCCGTCTCTATAAAAAATTAGCCAGGCGTGGTGGCACACGCCTGTAGTCTCAGCTGCTGGAGTGGCTGAGGTGGCAGGATCACTTGAGCCTGGGAGGTGGAGGCTGCAGCGAGCCAACATTGTGCCACTGCACTCCAGCCTGGGTGACAGAGTC... |
Task1_train_32646 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GCCTGACCCCTGCAGAGAGGCATTCCTGAGAGAGGGCTCAACAAATGCAATATGCTATAAAAAAAAATCTGTATAAATGAGTGATAAACACAATTTTCATTTCTGTAATATTTCTTTGCCTAGACTTGGTACATGGTAAAAAGGTCATTAAATTTTTACTTTTTTATCCATCGCTTTAAATAAGTATTTACTGGTTTAAACTTTATGCAAGGCGCTGTGATAGGCATTGGTCCACAGTAAGTGATCCAAAAATTCATATATTGTTGACTAGCTTTATTCAAAGCTCCTCAAAGATTCTACAGTATAAAGAGATATAGGCG... | GCCTGACCCCTGCAGAGAGGCATTCCTGAGAGAGGGCTCAACAAATGCAATATGCTATAAAAAAAAATCTGTATAAATGAGTGATAAACACAATTTTCATTTCTGTAATATTTCTTTGCCTAGACTTGGTACATGGTAAAAAGGTCATTAAATTTTTACTTTTTTATCCATCGCTTTAAATAAGTATTTACTGGTTTAAACTTTATGCAAGGCGCTGTGATAGGCATTGGTCCACAGTAAGTGATCCAAAAATTCATATATTGTTGACTAGCTTTATTCAAAGCTCCTCAAAGATTCTACAGTATAAAGAGATATAGGCG... |
Task1_train_32647 | A variant affecting Chromosome 1 has been observed. Determine if it's benign or associated with disease. | Benign | CTTGGTACATGGTAAAAAGGTCATTAAATTTTTACTTTTTTATCCATCGCTTTAAATAAGTATTTACTGGTTTAAACTTTATGCAAGGCGCTGTGATAGGCATTGGTCCACAGTAAGTGATCCAAAAATTCATATATTGTTGACTAGCTTTATTCAAAGCTCCTCAAAGATTCTACAGTATAAAGAGATATAGGCGTGCAAATAAATGAACGATGTTCACTTATTCAGTCAACAGATATTTCTTGAGAATATATGTGCCAGGCACTATTCTAAGCCCTGAGGATACAGTCATGAGCAGAAGCAAAAAAACCCCCTGCCTT... | CTTGGTACATGGTAAAAAGGTCATTAAATTTTTACTTTTTTATCCATCGCTTTAAATAAGTATTTACTGGTTTAAACTTTATGCAAGGCGCTGTGATAGGCATTGGTCCACAGTAAGTGATCCAAAAATTCATATATTGTTGACTAGCTTTATTCAAAGCTCCTCAAAGATTCTACAGTATAAAGAGATATAGGCGTGCAAATAAATGAACGATGTTCACTTATTCAGTCAACAGATATTTCTTGAGAATATATGTGCCAGGCACTATTCTAAGCCCTGAGGATACAGTCATGAGCAGAAGCAAAAAAACCCCCTGCCTT... |
Task1_train_32648 | A genomic change on Chromosome 1 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TTTATCCATCGCTTTAAATAAGTATTTACTGGTTTAAACTTTATGCAAGGCGCTGTGATAGGCATTGGTCCACAGTAAGTGATCCAAAAATTCATATATTGTTGACTAGCTTTATTCAAAGCTCCTCAAAGATTCTACAGTATAAAGAGATATAGGCGTGCAAATAAATGAACGATGTTCACTTATTCAGTCAACAGATATTTCTTGAGAATATATGTGCCAGGCACTATTCTAAGCCCTGAGGATACAGTCATGAGCAGAAGCAAAAAAACCCCCTGCCTTGGGGAGCTTACATTCTAGTGAGAGAGATGATAAACATG... | TTTATCCATCGCTTTAAATAAGTATTTACTGGTTTAAACTTTATGCAAGGCGCTGTGATAGGCATTGGTCCACAGTAAGTGATCCAAAAATTCATATATTGTTGACTAGCTTTATTCAAAGCTCCTCAAAGATTCTACAGTATAAAGAGATATAGGCGTGCAAATAAATGAACGATGTTCACTTATTCAGTCAACAGATATTTCTTGAGAATATATGTGCCAGGCACTATTCTAAGCCCTGAGGATACAGTCATGAGCAGAAGCAAAAAAACCCCCTGCCTTGGGGAGCTTACATTCTAGTGAGAGAGATGATAAACATG... |
Task1_train_32649 | A genomic variant on Chromosome 1 is under review. What is the biological outcome — benign or pathogenic? | Benign | TGAATAGTAGGAAGTCCCCAGCACCAGAGACTGGGTGACCCTTTTGGGGAAGGGTTGAACAGGTGTCACAAATCAGGAGGGTTCTCATGTGGTTTTTTTTGTTTGTTTTTTGTTTTGTTTTGTTTTTTGAGACAGAGTCTTGCTCTGTTGCCCAGGCTGGAGTGTAGTGGCATGATCTTGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGCGATTCTCATGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGAGTTCACCGCCATGCCCAGCTAATTGTTGTATTTTTAGTAGAGACGAGGTTTCATCATGTTGACCA... | TGAATAGTAGGAAGTCCCCAGCACCAGAGACTGGGTGACCCTTTTGGGGAAGGGTTGAACAGGTGTCACAAATCAGGAGGGTTCTCATGTGGTTTTTTTTGTTTGTTTTTTGTTTTGTTTTGTTTTTTGAGACAGAGTCTTGCTCTGTTGCCCAGGCTGGAGTGTAGTGGCATGATCTTGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGCGATTCTCATGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGAGTTCACCGCCATGCCCAGCTAATTGTTGTATTTTTAGTAGAGACGAGGTTTCATCATGTTGACCA... |
Task1_train_32650 | The following genetic variant occurs on Chromosome 1. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GTCTTATGAGAGGTTCTAGAGATGCTTTTGCTTTCTTGATAAAGAGCCATTTGCAGCTGGCACTTCCCCTGTCCCCTCCAGTCTTGAACATGGATGCGATGCCTGGAGCTATGGCAGCCATCTTGCAGCTGTGAGGCTCAGAGAGTCCCAGAGATAACATTTGGAACAGTGTTGAGCCCCTGGACCAATACAGCAGCTGCCTAGCTCCAGGCTTCCTGTTGAGTGAGGAAAAACAAGCACCATGTTTTCAATGAGTAGTTCTGAATGATACAAGCAGGGCTGGTAGACATCCCCACAGTTATACCAATTTTTTTGCCATA... | GTCTTATGAGAGGTTCTAGAGATGCTTTTGCTTTCTTGATAAAGAGCCATTTGCAGCTGGCACTTCCCCTGTCCCCTCCAGTCTTGAACATGGATGCGATGCCTGGAGCTATGGCAGCCATCTTGCAGCTGTGAGGCTCAGAGAGTCCCAGAGATAACATTTGGAACAGTGTTGAGCCCCTGGACCAATACAGCAGCTGCCTAGCTCCAGGCTTCCTGTTGAGTGAGGAAAAACAAGCACCATGTTTTCAATGAGTAGTTCTGAATGATACAAGCAGGGCTGGTAGACATCCCCACAGTTATACCAATTTTTTTGCCATA... |
Task1_train_32651 | This mutation on Chromosome 1 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GATGGAGGGCAGTGAGAAGAAAGAAACAGAGGTTGTCACGAACATTCCCCAGTCACTGGCAGAAGCCAGAGCACTCTAGTCCCCATCACCAACTTCCAGTGGCAGAAATACAAGGAGACACTAAATATAAAGTCATGCATGCCTGTAATCCCAGCAAGCACTTTGGGAGGCCAAGAGGGGAGGTTTGCTTAAGCCCAGGAGTTTGAGCCCAGCCTGGGCAATATTGCAAGACCCCATCTCTATCTTTATAAAAAGCAAAAATATGGCCAGGTACAGTGGCTCACACCTATAATCCCACTACTTTGAGAGGCTGAGGCAGG... | GATGGAGGGCAGTGAGAAGAAAGAAACAGAGGTTGTCACGAACATTCCCCAGTCACTGGCAGAAGCCAGAGCACTCTAGTCCCCATCACCAACTTCCAGTGGCAGAAATACAAGGAGACACTAAATATAAAGTCATGCATGCCTGTAATCCCAGCAAGCACTTTGGGAGGCCAAGAGGGGAGGTTTGCTTAAGCCCAGGAGTTTGAGCCCAGCCTGGGCAATATTGCAAGACCCCATCTCTATCTTTATAAAAAGCAAAAATATGGCCAGGTACAGTGGCTCACACCTATAATCCCACTACTTTGAGAGGCTGAGGCAGG... |
Task1_train_32652 | This mutation on Chromosome 1 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TACACCCCTGGTTCAGCTGGTCTCTGTCCAAATAATGTCAAGTCCTGATCTGTGCCAGACACTGCTGCCATGCCAAGCACCTGATACATAGCATATTTAATCTGCACACACCCCTTACAAGGTAAATGTCATTTCCATATTCAAGAAAAATATTGCATGCCTAGCATGTGCCATGCACTGTTCTGGGCCCTAAGAAGAAAACACGGATAATTTAAGGAATTTGCCCACGGTCACCCACCTGGTGCTATAGGTCAGCTTCCCGAGGAAACACTTAGAGACTTTTATTTGGGGAGAACCTTTAGGACAGGAACCTGTGGAGA... | TACACCCCTGGTTCAGCTGGTCTCTGTCCAAATAATGTCAAGTCCTGATCTGTGCCAGACACTGCTGCCATGCCAAGCACCTGATACATAGCATATTTAATCTGCACACACCCCTTACAAGGTAAATGTCATTTCCATATTCAAGAAAAATATTGCATGCCTAGCATGTGCCATGCACTGTTCTGGGCCCTAAGAAGAAAACACGGATAATTTAAGGAATTTGCCCACGGTCACCCACCTGGTGCTATAGGTCAGCTTCCCGAGGAAACACTTAGAGACTTTTATTTGGGGAGAACCTTTAGGACAGGAACCTGTGGAGA... |
Task1_train_32653 | Consider a variant on Chromosome 1. Determine its clinical classification and disease relevance. | Benign | GTCTGATCTTTTACATCCAACCCCCAGCCCCAACTCCAAGCCCCCAGTGCTTGTACCCAGTGAGCCCAGGGCTGGGCAGAGCAACGCTCATCCGCCTGTAACCCCACCCTGCCCAGCCACTCTGCTCAAGTCCAGGGGAGCCCCATGGCCTGAACCCCAAGAGGCCCAGCTCCCCTCAGTTCAGGGTCAGAGCCCTCTGAGGGACCCCAGGTATGTTCTGGGCTCAATCTCCTGGAGTCTGTGGAATCTGGGAACACAGCCCACCACTTCATGGGACAGCCGAGACTGGGGCGGGGGATTCCTCAGGTCACCAGGGAGCC... | GTCTGATCTTTTACATCCAACCCCCAGCCCCAACTCCAAGCCCCCAGTGCTTGTACCCAGTGAGCCCAGGGCTGGGCAGAGCAACGCTCATCCGCCTGTAACCCCACCCTGCCCAGCCACTCTGCTCAAGTCCAGGGGAGCCCCATGGCCTGAACCCCAAGAGGCCCAGCTCCCCTCAGTTCAGGGTCAGAGCCCTCTGAGGGACCCCAGGTATGTTCTGGGCTCAATCTCCTGGAGTCTGTGGAATCTGGGAACACAGCCCACCACTTCATGGGACAGCCGAGACTGGGGCGGGGGATTCCTCAGGTCACCAGGGAGCC... |
Task1_train_32654 | A variant on Chromosome 1 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TCATCCGCCTGTAACCCCACCCTGCCCAGCCACTCTGCTCAAGTCCAGGGGAGCCCCATGGCCTGAACCCCAAGAGGCCCAGCTCCCCTCAGTTCAGGGTCAGAGCCCTCTGAGGGACCCCAGGTATGTTCTGGGCTCAATCTCCTGGAGTCTGTGGAATCTGGGAACACAGCCCACCACTTCATGGGACAGCCGAGACTGGGGCGGGGGATTCCTCAGGTCACCAGGGAGCCAGACTGAGCAGCCTTCTTACCCCCGCTAGAGCCCTGCTCTGGCCTAGCGCGTTAGTGGCTATGCTGCTGCTGGTGTCAGCGACTTGC... | TCATCCGCCTGTAACCCCACCCTGCCCAGCCACTCTGCTCAAGTCCAGGGGAGCCCCATGGCCTGAACCCCAAGAGGCCCAGCTCCCCTCAGTTCAGGGTCAGAGCCCTCTGAGGGACCCCAGGTATGTTCTGGGCTCAATCTCCTGGAGTCTGTGGAATCTGGGAACACAGCCCACCACTTCATGGGACAGCCGAGACTGGGGCGGGGGATTCCTCAGGTCACCAGGGAGCCAGACTGAGCAGCCTTCTTACCCCCGCTAGAGCCCTGCTCTGGCCTAGCGCGTTAGTGGCTATGCTGCTGCTGGTGTCAGCGACTTGC... |
Task1_train_32655 | This mutation occurs on Chromosome 1. Does this change lead to a known medical condition, or is it benign? | Benign | GTGGGTGGGTCCTCTACCTCCTCTCTCCATTCTTCTCCCTGCAGCCCAGGGCCACTCACACTTGCAGGGCCCTGATTAGAGCAGCAGAGTTCTGTAATGGTTGGCAGAGCAAGGGGAATCCCAAGGATCTTCCTGTCCCAAATCCCAGAACACAGACAGGAAAATCGAGGCCCAGGAGGGGAAGGGACTTGCCCCAGGTCACTGAGCTACATAGATTCCAGTGTGGGACTTGACTTCCAGGCCCCTGAGTCTCACATCCAGCCTCAGCAGCCAGGTTTTTGTGGGAATGGAGGGAAGGCAGCATGAGCGCCTGATCTTGG... | GTGGGTGGGTCCTCTACCTCCTCTCTCCATTCTTCTCCCTGCAGCCCAGGGCCACTCACACTTGCAGGGCCCTGATTAGAGCAGCAGAGTTCTGTAATGGTTGGCAGAGCAAGGGGAATCCCAAGGATCTTCCTGTCCCAAATCCCAGAACACAGACAGGAAAATCGAGGCCCAGGAGGGGAAGGGACTTGCCCCAGGTCACTGAGCTACATAGATTCCAGTGTGGGACTTGACTTCCAGGCCCCTGAGTCTCACATCCAGCCTCAGCAGCCAGGTTTTTGTGGGAATGGAGGGAAGGCAGCATGAGCGCCTGATCTTGG... |
Task1_train_32656 | A variant was discovered on Chromosome 1. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CCGCTGGTCACTTGGTGAATTGTATTTTGACAAACTGGCTTTCCCCTTCCCACCCCATCTATTTTCTCCAGAGCAGGCTTGTAGCTCTTTATACATGGGCTTCCTGCTGAAGGTGTCTTTGCAAAAAGGGCCATGTTGCCTTAAAAAGCCCTGGCCCAGCTGACTCAGGCCTGCTGGTTGTCCCCTTCCAGAAGGCAGAGAGGTGATTTGGTGGTGGATGTCGTGTAGGGGGAGGGCGGTTGTGCATGTGGTAGGTGGGCTTCTTGGAGGGAGGCTGGGGTGGGCCTTGAAGGCCAGACCAAATCTTGATACTTGATGGG... | CCGCTGGTCACTTGGTGAATTGTATTTTGACAAACTGGCTTTCCCCTTCCCACCCCATCTATTTTCTCCAGAGCAGGCTTGTAGCTCTTTATACATGGGCTTCCTGCTGAAGGTGTCTTTGCAAAAAGGGCCATGTTGCCTTAAAAAGCCCTGGCCCAGCTGACTCAGGCCTGCTGGTTGTCCCCTTCCAGAAGGCAGAGAGGTGATTTGGTGGTGGATGTCGTGTAGGGGGAGGGCGGTTGTGCATGTGGTAGGTGGGCTTCTTGGAGGGAGGCTGGGGTGGGCCTTGAAGGCCAGACCAAATCTTGATACTTGATGGG... |
Task1_train_32657 | Given this context: Chromosome 1 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CTGGTGAATTCAGTGCTAACCCACAGGTACCTCCTCCCTCCAGCCTGGCCCTGAGCCCCGCATTGGGGCTTTAAGAGTCGATGTGCCTTGCATCCCCCTGGTGAGGAATCTGTGCTAGAGGGGGCAGGGTCTCGGCCTTGGTTGGGCAGAACAGGCCCCCACTTTCTTCTGTGGCTGACCCCTGTCCCCTTGCTACCCTTCCTTCACTCAGGGACCCCTATGTCATCGCGCTGAGGTCGGTCACGCTGCCCACACACCGAGAGACGCCAGAGTACAGACGCGGAGAGACCCTCTGCTCAGGCTTCTGCCTCTGGCGCGAG... | CTGGTGAATTCAGTGCTAACCCACAGGTACCTCCTCCCTCCAGCCTGGCCCTGAGCCCCGCATTGGGGCTTTAAGAGTCGATGTGCCTTGCATCCCCCTGGTGAGGAATCTGTGCTAGAGGGGGCAGGGTCTCGGCCTTGGTTGGGCAGAACAGGCCCCCACTTTCTTCTGTGGCTGACCCCTGTCCCCTTGCTACCCTTCCTTCACTCAGGGACCCCTATGTCATCGCGCTGAGGTCGGTCACGCTGCCCACACACCGAGAGACGCCAGAGTACAGACGCGGAGAGACCCTCTGCTCAGGCTTCTGCCTCTGGCGCGAG... |
Task1_train_32658 | This sequence change occurs on Chromosome 1. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TGAAGCAGCAGTCATTAGCTGGGGAAGGGGAGTGGAGATGGATGCCCAGCCTGTGGAAGACCCAGACCTAACTGGGAGAGCCTGCCTCTTTGGAGGAAGTCAAAAGAACTCTGCAAGGGTGGAACGGAAAAGGAAAGGGACATATGGAGGGGCAAAAAGGGTGAAAAGGGGACTGGGGCCAGATACAGAGGGCCTTTTGGGTCTGCTAACAACTGGAGGACTCTATCCTAAAGATAACAGGAAGCCATGGAGGGGTTTAGGCAAGGGGATGGCTTAGAGATGGTGTTGGCTGCCCAGAAGGCCAGTGGGGTGAGTGACCT... | TGAAGCAGCAGTCATTAGCTGGGGAAGGGGAGTGGAGATGGATGCCCAGCCTGTGGAAGACCCAGACCTAACTGGGAGAGCCTGCCTCTTTGGAGGAAGTCAAAAGAACTCTGCAAGGGTGGAACGGAAAAGGAAAGGGACATATGGAGGGGCAAAAAGGGTGAAAAGGGGACTGGGGCCAGATACAGAGGGCCTTTTGGGTCTGCTAACAACTGGAGGACTCTATCCTAAAGATAACAGGAAGCCATGGAGGGGTTTAGGCAAGGGGATGGCTTAGAGATGGTGTTGGCTGCCCAGAAGGCCAGTGGGGTGAGTGACCT... |
Task1_train_32659 | The following genetic variant occurs on Chromosome 1. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | AGGAATAGCATTCCAGGCAGAGGATGACAAAGTGGCAGTGTGACTGGAGCCCAGAGGGTGAGGTGAGAGTTCTGGGAAGTGAGGCTGGAATGCCAGCATCCCGGAGGTGGTGCCCTTGGAGAAGACTGGGGTTGTGGGGGTGACTGAAAAAAGGAGGCCGCCCTCTTGTAGTATCAGATTTAGCCAGCAGAGGACAGTGCTGCATAGTAATCTGCAGAGATGGGCAGGAAGGAGGAGGCAGGTGGTGAGCCAGGCTTTCTTGGTGGTTGTGGTATAACCCCAAGGACCACTGGCTTCAGGGTGTGTGCAGACTCAGGGAG... | AGGAATAGCATTCCAGGCAGAGGATGACAAAGTGGCAGTGTGACTGGAGCCCAGAGGGTGAGGTGAGAGTTCTGGGAAGTGAGGCTGGAATGCCAGCATCCCGGAGGTGGTGCCCTTGGAGAAGACTGGGGTTGTGGGGGTGACTGAAAAAAGGAGGCCGCCCTCTTGTAGTATCAGATTTAGCCAGCAGAGGACAGTGCTGCATAGTAATCTGCAGAGATGGGCAGGAAGGAGGAGGCAGGTGGTGAGCCAGGCTTTCTTGGTGGTTGTGGTATAACCCCAAGGACCACTGGCTTCAGGGTGTGTGCAGACTCAGGGAG... |
Task1_train_32660 | A variant was discovered on Chromosome 1. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | ACGCTGCTGTTAATGAGGCCACAGGATCTCATGGGAAAGGCAACAACAAGCAGTCACAGGGGCTCGGAGCTGGAGAGTGACACACTCAGCTTTGCCACATGGTGCTGATGGACATCAGACGGAGACTTCCAGCAATCTGTTGGTTTTGCAAGTCTGAAGCTCCGGGCAGAGCTGAGCCTGGTATCCAATGTGCAATCCCAGTGCATGGGAGGCCAGGGGGCTGCCCTGCCCCCCTCAGCCTGGGAAGTAATGACCCTTTGCTCCCTCAGCTCCTCCAGATGGAGCAGGTGCGCCGGATCCCCGAGGAATACTCTCTGGGG... | ACGCTGCTGTTAATGAGGCCACAGGATCTCATGGGAAAGGCAACAACAAGCAGTCACAGGGGCTCGGAGCTGGAGAGTGACACACTCAGCTTTGCCACATGGTGCTGATGGACATCAGACGGAGACTTCCAGCAATCTGTTGGTTTTGCAAGTCTGAAGCTCCGGGCAGAGCTGAGCCTGGTATCCAATGTGCAATCCCAGTGCATGGGAGGCCAGGGGGCTGCCCTGCCCCCCTCAGCCTGGGAAGTAATGACCCTTTGCTCCCTCAGCTCCTCCAGATGGAGCAGGTGCGCCGGATCCCCGAGGAATACTCTCTGGGG... |
Task1_train_32661 | This sequence change occurs on Chromosome 1. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CCACCACGCCTGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACTGTGTTAGCCAGGATGGTCTCGAACTCCTGACCTCATGAACTGCCCGCCTCAGCCCCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTGCCCGGCCCTGGACACACCTCTTAACACTTGCAGTACCCAGCATGGCGGGCCTGTGCACACCTCCATGCCTCTCTCCACATATGAGCTCCCACTGCCTAAAACGCTGAGTCCTCTATCCATCTGCAGAGACCTTCCTCAGCTCTGATCTCAGCTCTGCATCACCTTGAATCCCACCCCT... | CCACCACGCCTGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACTGTGTTAGCCAGGATGGTCTCGAACTCCTGACCTCATGAACTGCCCGCCTCAGCCCCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTGCCCGGCCCTGGACACACCTCTTAACACTTGCAGTACCCAGCATGGCGGGCCTGTGCACACCTCCATGCCTCTCTCCACATATGAGCTCCCACTGCCTAAAACGCTGAGTCCTCTATCCATCTGCAGAGACCTTCCTCAGCTCTGATCTCAGCTCTGCATCACCTTGAATCCCACCCCT... |
Task1_train_32662 | A genetic alteration is present on Chromosome 1. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | CTGGCTTTGAGCTTGGTCTTCACAGATTCTTGTCAGATATGGACATGCAGAGACCCTAGGGGGCCAAGGATGGAAAACTTGGTTATGTTCCTTATCTAAGATGCAGGAGCAATGAAAGTAGTTGGCATTGCTAGGGTAGTTCAAGCTTGCTCCATCTTTCCATACAATTCAGGCAGAGAGTAGCTTTTTTTTTTCTTTAAAACCAGCTTCTACATTAAGGACACAAGAGACCAGCTCTTAATATTCACCCCATCTTGGCTCTAGGATCCAACTCTGTACCTACGATAAGGTCACCGTGGCAGTTGAAGCCTGCTGCCCCG... | CTGGCTTTGAGCTTGGTCTTCACAGATTCTTGTCAGATATGGACATGCAGAGACCCTAGGGGGCCAAGGATGGAAAACTTGGTTATGTTCCTTATCTAAGATGCAGGAGCAATGAAAGTAGTTGGCATTGCTAGGGTAGTTCAAGCTTGCTCCATCTTTCCATACAATTCAGGCAGAGAGTAGCTTTTTTTTTTCTTTAAAACCAGCTTCTACATTAAGGACACAAGAGACCAGCTCTTAATATTCACCCCATCTTGGCTCTAGGATCCAACTCTGTACCTACGATAAGGTCACCGTGGCAGTTGAAGCCTGCTGCCCCG... |
Task1_train_32663 | 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 | GATGGTCATGGGTCACAGTCTTGGGCATAAGAGGGATAGGGGTGGGTGGGGGATAGAAGTGGACAGGGGTGCGTGTGGCCTGCTGTGGAGTCACCTCCTGGCCTCTGCTGCAATGGTGGTGAGAGGAGAAGGAGGGTGAGAGAGAATGTCACCATTCAAAGTGGTGAACCATGGTGACCCATGAGGTAGAATTCAGGAGACTTAGGGTGGCCTCCCTGCCATATTTCACAGGTACCCGGAATGCCACCGTTAGTGTTGAAGCATTGTCCAAGTGGATATCAGAGTGACTCGTGTAACAAGTGACACACAAACCTTTAACA... | GATGGTCATGGGTCACAGTCTTGGGCATAAGAGGGATAGGGGTGGGTGGGGGATAGAAGTGGACAGGGGTGCGTGTGGCCTGCTGTGGAGTCACCTCCTGGCCTCTGCTGCAATGGTGGTGAGAGGAGAAGGAGGGTGAGAGAGAATGTCACCATTCAAAGTGGTGAACCATGGTGACCCATGAGGTAGAATTCAGGAGACTTAGGGTGGCCTCCCTGCCATATTTCACAGGTACCCGGAATGCCACCGTTAGTGTTGAAGCATTGTCCAAGTGGATATCAGAGTGACTCGTGTAACAAGTGACACACAAACCTTTAACA... |
Task1_train_32664 | This alteration on Chromosome 1 may affect genome function. Does it lead to a disease or is it benign? | Benign | TGGCACACGTCTGTAATCCCAGCTACTTGGAAGGCTGAGGCGGGAAGATCGCTTGAACCCAGGAGATGGAGGTTGCAGTGGGCCAAGATCGTGCCATTGCACTCCAGCATGGGCAACAAGAGCGAAACTCCCTCTCAAAAAAAAAAAAAAAAAAGGGGGGGGGCAGGTGGCACCTCCTAATGGGTGGCGCCCTTAGTTTCCCCCAAGAAGAGGGAAATCAAGTGAAGGTTCTATTGATGAGCTCTATTTCAGAGCATTTGGGAGGCCTTTTGGGCCAAGCGGACCAAGAAGGAGGCCTACTAGAAAAGTAGCAGAGAGGC... | TGGCACACGTCTGTAATCCCAGCTACTTGGAAGGCTGAGGCGGGAAGATCGCTTGAACCCAGGAGATGGAGGTTGCAGTGGGCCAAGATCGTGCCATTGCACTCCAGCATGGGCAACAAGAGCGAAACTCCCTCTCAAAAAAAAAAAAAAAAAAGGGGGGGGGCAGGTGGCACCTCCTAATGGGTGGCGCCCTTAGTTTCCCCCAAGAAGAGGGAAATCAAGTGAAGGTTCTATTGATGAGCTCTATTTCAGAGCATTTGGGAGGCCTTTTGGGCCAAGCGGACCAAGAAGGAGGCCTACTAGAAAAGTAGCAGAGAGGC... |
Task1_train_32665 | A genetic alteration is present on Chromosome 1. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | CCCACCATGTGCCAGTTCCTATGCTGGGTACAGGAGGTACCGTGGTAACAAGATAGATGAGGTCCCTGCTCTGGCAGAACTTAACATTCCAGTAGGGGAGGCAGTCAATAGTAAACAGTTCTATTTCAAGTGGTAAGTGCTATGACAAAATAAATATGGCAATGGGATAGAGGTGATTGGGGAGGATTATTTTAGGTAGGATGGCAGCACCGATTTTGTGAGAGTCTATGTCAACAAGCAGTTTGGGAAGAATGGCAGGTGGCCCCAACTGCCAAGCATCACATTACAAATGATCTCAAACCCTTGCTTTCCTGAATTCC... | CCCACCATGTGCCAGTTCCTATGCTGGGTACAGGAGGTACCGTGGTAACAAGATAGATGAGGTCCCTGCTCTGGCAGAACTTAACATTCCAGTAGGGGAGGCAGTCAATAGTAAACAGTTCTATTTCAAGTGGTAAGTGCTATGACAAAATAAATATGGCAATGGGATAGAGGTGATTGGGGAGGATTATTTTAGGTAGGATGGCAGCACCGATTTTGTGAGAGTCTATGTCAACAAGCAGTTTGGGAAGAATGGCAGGTGGCCCCAACTGCCAAGCATCACATTACAAATGATCTCAAACCCTTGCTTTCCTGAATTCC... |
Task1_train_32666 | This alteration on Chromosome 1 may affect genome function. Does it lead to a disease or is it benign? | Benign | CCAAATCCCAAACTCTCTCTGGAGGTTTGTGTAGGGGGCTGACCACAGCTGCTCTGTGCAGAACTGTGGAGCAGCTGCTGGGCCATGCCCCAGGACACAGCACAGGGTTGGCAGCCACACCCCCATGAAGCAATCGGCTCCCTCCCTGGAGTGCTGGGCACCCTGCTTAGCACTCTCTCATCTGGATGTTCACTCACTGGGGAATCCCCACTGTGGCCGTGTTCCCAGAGAGGGAAGAGCCAGCCTCTGATAGCTACCCCTGAATCACTGCTTTCCTGCTCACCTCCTCCAGGAAGGCTTCCCCCAGTGAACGGCCTCCT... | CCAAATCCCAAACTCTCTCTGGAGGTTTGTGTAGGGGGCTGACCACAGCTGCTCTGTGCAGAACTGTGGAGCAGCTGCTGGGCCATGCCCCAGGACACAGCACAGGGTTGGCAGCCACACCCCCATGAAGCAATCGGCTCCCTCCCTGGAGTGCTGGGCACCCTGCTTAGCACTCTCTCATCTGGATGTTCACTCACTGGGGAATCCCCACTGTGGCCGTGTTCCCAGAGAGGGAAGAGCCAGCCTCTGATAGCTACCCCTGAATCACTGCTTTCCTGCTCACCTCCTCCAGGAAGGCTTCCCCCAGTGAACGGCCTCCT... |
Task1_train_32667 | Consider this mutation on Chromosome 1. Is this a benign change or a disease-causing variant? | Benign | CCTCCCCATCTCCATCCCCAGGCCCTGCGTCCTCTGCCCAATACTCTTTGGGCCTCCCTGTTGTCCAGCTCTCTCCGCGGCTCCATGACTGACAACTTGAGCAAGGCTAATGTGAATGGGAGCGGTTGAGGGCTCAGACCTCTCACCCGAGGAACATCCACAGAGTGTGCCGCATGCCCGGTGCAGTGTGGCTGCGGGGACACAGACACGGAGCCTCGGCCCTGAGGAGCTGGGGGGCAGTGACCGTCCCTCCTCTGACCCACCACTCCTCCAGTGTCAGGACACTGCGGGTATCTAGGGGAAGGAATCTTGTTCCACTT... | CCTCCCCATCTCCATCCCCAGGCCCTGCGTCCTCTGCCCAATACTCTTTGGGCCTCCCTGTTGTCCAGCTCTCTCCGCGGCTCCATGACTGACAACTTGAGCAAGGCTAATGTGAATGGGAGCGGTTGAGGGCTCAGACCTCTCACCCGAGGAACATCCACAGAGTGTGCCGCATGCCCGGTGCAGTGTGGCTGCGGGGACACAGACACGGAGCCTCGGCCCTGAGGAGCTGGGGGGCAGTGACCGTCCCTCCTCTGACCCACCACTCCTCCAGTGTCAGGACACTGCGGGTATCTAGGGGAAGGAATCTTGTTCCACTT... |
Task1_train_32668 | A variant on Chromosome 1 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | CAGAGCAACCGGAAGAATAGAACTGCTTTTAAGTTGAGAAAACTCTAGGATGATATGGGCAGGATTAGAGGAGCTCAGTTCTGGAAATGAGAAGTTTGGGATGTCTATTTGATATCCAACTGGAGACATCAGGACAGTGGTACAGGCCATAGACCCAAATTTAGGTGTTGTCAACATATAGATGGAATTTAAAACTGTGAAACTGCACGAGATCACCAAGGGAATGAATGGAGATAGAGAAGAGATGATAGGACCTGAGCCCTGGGGTGCTCTCATGTTAGAGAATGATTAGTAATGGTCCCCGTTCACCAAAGCCAACA... | CAGAGCAACCGGAAGAATAGAACTGCTTTTAAGTTGAGAAAACTCTAGGATGATATGGGCAGGATTAGAGGAGCTCAGTTCTGGAAATGAGAAGTTTGGGATGTCTATTTGATATCCAACTGGAGACATCAGGACAGTGGTACAGGCCATAGACCCAAATTTAGGTGTTGTCAACATATAGATGGAATTTAAAACTGTGAAACTGCACGAGATCACCAAGGGAATGAATGGAGATAGAGAAGAGATGATAGGACCTGAGCCCTGGGGTGCTCTCATGTTAGAGAATGATTAGTAATGGTCCCCGTTCACCAAAGCCAACA... |
Task1_train_32669 | A variant on Chromosome 1 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GAGAATGAACATCTGCTGAGCGCTCACTAGAGTGAACCACCACGTTCAGTATTTCTATGTGTATTTGTCACTTGATCTTCACAACACATCTGAAGAGAAGAGTTTAGCATTTGGGGAGGCAATACTGCATATGGTTAAAGAACATAGACTAGCTGCCTGCATGGGTTCTCCCTGTAACTAGGTATGTGGACTTGGGCAAGTACTTCACTTCTGTCTGTTTCAGTTCTCACCTATGAAATGGGGGTAAAAATAGTACCCAACTCAAAGAGCCATTGTGGGGATTAAATTCCAAAGTACATATTCACTGTCCTTTCCACTCA... | GAGAATGAACATCTGCTGAGCGCTCACTAGAGTGAACCACCACGTTCAGTATTTCTATGTGTATTTGTCACTTGATCTTCACAACACATCTGAAGAGAAGAGTTTAGCATTTGGGGAGGCAATACTGCATATGGTTAAAGAACATAGACTAGCTGCCTGCATGGGTTCTCCCTGTAACTAGGTATGTGGACTTGGGCAAGTACTTCACTTCTGTCTGTTTCAGTTCTCACCTATGAAATGGGGGTAAAAATAGTACCCAACTCAAAGAGCCATTGTGGGGATTAAATTCCAAAGTACATATTCACTGTCCTTTCCACTCA... |
Task1_train_32670 | A mutation found on Chromosome 1 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AACATTTGAAACTAAACAAATATATGGAAATTAAACAACATGCTCCTGAACAACCAATGGGTGAAGGAAGAAATTAAGGATAATACTTAAAAATTCTTTGAAACAAATGAAAATAGAAACACAACATATCAAACTTATAGGACACAGCAAAAACAATATTAAGAGGCAAGTTTATAGCAATAAATGCCTACATCAAAAACTAGAAAGATTTCAAAAAACAATCTAATGATTTGTCTCAAAGAATTAGAAAAGGAAGAACAAACCAAATCCAAAGTTAGTAGAAGAAAAGAAATAATAAAGATCAAAGCTGACATAAACAA... | AACATTTGAAACTAAACAAATATATGGAAATTAAACAACATGCTCCTGAACAACCAATGGGTGAAGGAAGAAATTAAGGATAATACTTAAAAATTCTTTGAAACAAATGAAAATAGAAACACAACATATCAAACTTATAGGACACAGCAAAAACAATATTAAGAGGCAAGTTTATAGCAATAAATGCCTACATCAAAAACTAGAAAGATTTCAAAAAACAATCTAATGATTTGTCTCAAAGAATTAGAAAAGGAAGAACAAACCAAATCCAAAGTTAGTAGAAGAAAAGAAATAATAAAGATCAAAGCTGACATAAACAA... |
Task1_train_32671 | A variant has been detected on Chromosome 1. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TGTTCTCCAACTGGTCATTAATTACAATCTCTTCCTACAGAGTTTACAAATCTCTTACTGCTGTTATTAACTGAAAGGCAGGACAGACCTATGGACAGGTTTGATCTTCACCTCTCCTTGCTACCTTTGCCACTTTGTTAATGAGCAGCTAAGGAGACAGAGGTGGGTAAGAAGAGAAGTGAGCTGCACTGCTCCACAACTCACCCATGGAATCACCTGGAAATACTGCACGGATAACAGTAACAATGTGAAAACCACCTCTGCTTATTGAACACCAATAATATACCAGAAACAGGGCTGGGGGCTTCTTTACACATTCT... | TGTTCTCCAACTGGTCATTAATTACAATCTCTTCCTACAGAGTTTACAAATCTCTTACTGCTGTTATTAACTGAAAGGCAGGACAGACCTATGGACAGGTTTGATCTTCACCTCTCCTTGCTACCTTTGCCACTTTGTTAATGAGCAGCTAAGGAGACAGAGGTGGGTAAGAAGAGAAGTGAGCTGCACTGCTCCACAACTCACCCATGGAATCACCTGGAAATACTGCACGGATAACAGTAACAATGTGAAAACCACCTCTGCTTATTGAACACCAATAATATACCAGAAACAGGGCTGGGGGCTTCTTTACACATTCT... |
Task1_train_32672 | This sequence change occurs on Chromosome 1. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TAAGCCTTATTAGTAACAGCCGTTAGAGCTGCATGTGTATGAACTCATTTATTTTCCCAAGAACCTTATGACATAAATGCTATTATGAGTCCCAATTTACAGATGAGGAAAACAGGGCAGAAGGAAGGTTGGATAATTTGCTCAAGGTCACCTAGCTGGGGAATGAAAGAGACAGGATTTGGACCCGGGACCCAATCTCTTAAACATTACACCCTACTGAGTCACATCCTAAGAGTGAGGAAATTTGGGGAATGAGAGCAGAGGGTCTGAGACAACTTCAGTAAGTATCATTTTGGGGAGTGGAAAGTGGGGTATGTACC... | TAAGCCTTATTAGTAACAGCCGTTAGAGCTGCATGTGTATGAACTCATTTATTTTCCCAAGAACCTTATGACATAAATGCTATTATGAGTCCCAATTTACAGATGAGGAAAACAGGGCAGAAGGAAGGTTGGATAATTTGCTCAAGGTCACCTAGCTGGGGAATGAAAGAGACAGGATTTGGACCCGGGACCCAATCTCTTAAACATTACACCCTACTGAGTCACATCCTAAGAGTGAGGAAATTTGGGGAATGAGAGCAGAGGGTCTGAGACAACTTCAGTAAGTATCATTTTGGGGAGTGGAAAGTGGGGTATGTACC... |
Task1_train_32673 | 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 | CTCATTTATTTTCCCAAGAACCTTATGACATAAATGCTATTATGAGTCCCAATTTACAGATGAGGAAAACAGGGCAGAAGGAAGGTTGGATAATTTGCTCAAGGTCACCTAGCTGGGGAATGAAAGAGACAGGATTTGGACCCGGGACCCAATCTCTTAAACATTACACCCTACTGAGTCACATCCTAAGAGTGAGGAAATTTGGGGAATGAGAGCAGAGGGTCTGAGACAACTTCAGTAAGTATCATTTTGGGGAGTGGAAAGTGGGGTATGTACCAGTTCATGGTTATCAATCTGGCCTGGCTTAAAGGAACAGATGT... | CTCATTTATTTTCCCAAGAACCTTATGACATAAATGCTATTATGAGTCCCAATTTACAGATGAGGAAAACAGGGCAGAAGGAAGGTTGGATAATTTGCTCAAGGTCACCTAGCTGGGGAATGAAAGAGACAGGATTTGGACCCGGGACCCAATCTCTTAAACATTACACCCTACTGAGTCACATCCTAAGAGTGAGGAAATTTGGGGAATGAGAGCAGAGGGTCTGAGACAACTTCAGTAAGTATCATTTTGGGGAGTGGAAAGTGGGGTATGTACCAGTTCATGGTTATCAATCTGGCCTGGCTTAAAGGAACAGATGT... |
Task1_train_32674 | A mutation has occurred on Chromosome 1. What is the medical relevance of this mutation? | Benign | TTGCATTTCCTTTATAGCATATGCCATGTTGTATTACAACTGATATAATTAAGAAAAATATGGCCGGGAGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATCATGAGGTCAGTAGATCAAGATCATCCTGGTTAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCTGAGCATGGTAGCATGTGCCTGTAGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGTGGAGGTTGAAGTGAGCCGAGATCATGCCACTGCACTCCAGCCTGGG... | TTGCATTTCCTTTATAGCATATGCCATGTTGTATTACAACTGATATAATTAAGAAAAATATGGCCGGGAGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATCATGAGGTCAGTAGATCAAGATCATCCTGGTTAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCTGAGCATGGTAGCATGTGCCTGTAGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGTGGAGGTTGAAGTGAGCCGAGATCATGCCACTGCACTCCAGCCTGGG... |
Task1_train_32675 | Given this context: Chromosome 1 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GTCCCCATTGCAAAGAAGTCTGCGGTTTACACACCTTCCTAGAATGGAGAAAGAGTATTACCCACAGCCACATGGTTGGCAAGAAAGGAACTAACATAGTATAAGCACCTACCAAGTGCCAGACCTTTTGTCAGGCCTTGCATGCTGCCCTGTTTTAATTAGTCATCCTGTATCCAGATAGATTGGTTATGGCACTAACAGTTTATTCCTCTATTGCCACCTCCCTCAGCAGAAGAGGCCAGTGTTGTATTCCAGAAAGCAGCAGGACAGTTTGGACTCTCTCTCCCTGGGGCTGGAAAGAGGGGGTGGGATGGGTGTGT... | GTCCCCATTGCAAAGAAGTCTGCGGTTTACACACCTTCCTAGAATGGAGAAAGAGTATTACCCACAGCCACATGGTTGGCAAGAAAGGAACTAACATAGTATAAGCACCTACCAAGTGCCAGACCTTTTGTCAGGCCTTGCATGCTGCCCTGTTTTAATTAGTCATCCTGTATCCAGATAGATTGGTTATGGCACTAACAGTTTATTCCTCTATTGCCACCTCCCTCAGCAGAAGAGGCCAGTGTTGTATTCCAGAAAGCAGCAGGACAGTTTGGACTCTCTCTCCCTGGGGCTGGAAAGAGGGGGTGGGATGGGTGTGT... |
Task1_train_32676 | This alteration on Chromosome 1 may affect genome function. Does it lead to a disease or is it benign? | Benign | TCTCAGGTATTTATTTTAGCAATTCAAGAACAGACTAATACAGCTGGGCAACAACAGCATTATAGTGAGTGCAAAATTGGATAATATATGCAAAGTGTTTAGTAGAGTTCCCAACACCTTCTGCTTCATAAATGTTAACTATTACTATTGCCTACTATAATGATAAACTTTCATAAAAAGTAACCAGGGTCCCTCTGATCATCTCTTTTCCCACTTAGGACTTCTGTTCACCTTCAATTATGCCCTACCTTGATAGTCATGCTCCTTGGAAGAAAAAGACACCCTAGGTAGGGCTATCTTATTGTCTAATCCCATGGAGT... | TCTCAGGTATTTATTTTAGCAATTCAAGAACAGACTAATACAGCTGGGCAACAACAGCATTATAGTGAGTGCAAAATTGGATAATATATGCAAAGTGTTTAGTAGAGTTCCCAACACCTTCTGCTTCATAAATGTTAACTATTACTATTGCCTACTATAATGATAAACTTTCATAAAAAGTAACCAGGGTCCCTCTGATCATCTCTTTTCCCACTTAGGACTTCTGTTCACCTTCAATTATGCCCTACCTTGATAGTCATGCTCCTTGGAAGAAAAAGACACCCTAGGTAGGGCTATCTTATTGTCTAATCCCATGGAGT... |
Task1_train_32677 | A mutation found on Chromosome 1 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GTACCCCACAGTCACACACATAAATGAACGTGAATGACTGAAAAGTAAGAGATAAGTGTAAGAGGGACAAGTGGCTAGTTTTTACAGCTAATAGGTAAAACATATCTTTAAAGCACATTAATAGTAAAAATCCCTGGGTGCAGTGGCTCACACCTATGATACCAGCACTTTGGGAGGCCGACGCAGGTGGATCACCTGAGGGCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACTCCATCTCTACTAAAAATGCAAAAATTAGTTGGGCATAGTGGTGGGCACCTGTAATCCCAGTTACTCAGGAGGCTGAGGTA... | GTACCCCACAGTCACACACATAAATGAACGTGAATGACTGAAAAGTAAGAGATAAGTGTAAGAGGGACAAGTGGCTAGTTTTTACAGCTAATAGGTAAAACATATCTTTAAAGCACATTAATAGTAAAAATCCCTGGGTGCAGTGGCTCACACCTATGATACCAGCACTTTGGGAGGCCGACGCAGGTGGATCACCTGAGGGCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACTCCATCTCTACTAAAAATGCAAAAATTAGTTGGGCATAGTGGTGGGCACCTGTAATCCCAGTTACTCAGGAGGCTGAGGTA... |
Task1_train_32678 | Consider a variant on Chromosome 1. Determine its clinical classification and disease relevance. | Benign | TCCCTGGGTGCAGTGGCTCACACCTATGATACCAGCACTTTGGGAGGCCGACGCAGGTGGATCACCTGAGGGCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACTCCATCTCTACTAAAAATGCAAAAATTAGTTGGGCATAGTGGTGGGCACCTGTAATCCCAGTTACTCAGGAGGCTGAGGTAGGAGAATCGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCTGAGCTCACTCCACTGCCCTGCAGCCTGGACAACAGAGCAAGACTCCATCTCAAAAAATATATGTAATAAGTAAAAGTCTTAGGAAAAC... | TCCCTGGGTGCAGTGGCTCACACCTATGATACCAGCACTTTGGGAGGCCGACGCAGGTGGATCACCTGAGGGCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACTCCATCTCTACTAAAAATGCAAAAATTAGTTGGGCATAGTGGTGGGCACCTGTAATCCCAGTTACTCAGGAGGCTGAGGTAGGAGAATCGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCTGAGCTCACTCCACTGCCCTGCAGCCTGGACAACAGAGCAAGACTCCATCTCAAAAAATATATGTAATAAGTAAAAGTCTTAGGAAAAC... |
Task1_train_32679 | This variant is present on Chromosome 1. Is the change likely to result in a pathogenic outcome? | Benign | AAGAAAGCTAGTATAAAACACTTTTTAGTATTTGTTCCCCAATATATCATGAGGAAACAGGTCAAAAGGAAGATGAGTACAAAGGAATCAATCACTGCCTTTCACAGAATCACGCAACTTCGGAGCTTGGAAGGGAATACTAAGCCATAAAATTCAGGCCCTTGATTTACTGGTGAGGAGCATGGGGTCCAGGTTATGTGTTTTGATTAAGGTCACACAGCAAAGTTGGTAACAGAGTTAGGGTAAGAGCTCAGGTTTCCTGACTTTTGGTATAGTTCCTCTTACACTCTCAGCCCTCAAACTAATTGTTTTATAAGCTA... | AAGAAAGCTAGTATAAAACACTTTTTAGTATTTGTTCCCCAATATATCATGAGGAAACAGGTCAAAAGGAAGATGAGTACAAAGGAATCAATCACTGCCTTTCACAGAATCACGCAACTTCGGAGCTTGGAAGGGAATACTAAGCCATAAAATTCAGGCCCTTGATTTACTGGTGAGGAGCATGGGGTCCAGGTTATGTGTTTTGATTAAGGTCACACAGCAAAGTTGGTAACAGAGTTAGGGTAAGAGCTCAGGTTTCCTGACTTTTGGTATAGTTCCTCTTACACTCTCAGCCCTCAAACTAATTGTTTTATAAGCTA... |
Task1_train_32680 | This mutation on Chromosome 1 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | AGCAAAGCTCTTTAACAACTATAAAGCACTATGTAAAGTCAGGAGTTGTTCCTTGCAAGTATTCTTTACTATGATGCCAACCTAACCCACATGTTGTACTTTCAGCACCTCCACCATCTGTAAGATAACTCAAGAACAAACCTCCTCCTTTAAGAATACAGCCATCTTTAAAAACCAAAGACTTATATTGTGTGGGTAAAATGAAGGTTACCGATTTATTATAGCAAGTTGTTTTCCTTTGGTAACCCTTCTAGGTTACAGCAGGAAGTTAACAATAGCAATAGGACAGGAAGGCTTTCCATACAAAAGAGAACAAAGGA... | AGCAAAGCTCTTTAACAACTATAAAGCACTATGTAAAGTCAGGAGTTGTTCCTTGCAAGTATTCTTTACTATGATGCCAACCTAACCCACATGTTGTACTTTCAGCACCTCCACCATCTGTAAGATAACTCAAGAACAAACCTCCTCCTTTAAGAATACAGCCATCTTTAAAAACCAAAGACTTATATTGTGTGGGTAAAATGAAGGTTACCGATTTATTATAGCAAGTTGTTTTCCTTTGGTAACCCTTCTAGGTTACAGCAGGAAGTTAACAATAGCAATAGGACAGGAAGGCTTTCCATACAAAAGAGAACAAAGGA... |
Task1_train_32681 | This variant lies on Chromosome 1. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AAGGGATGAGCAAAGGATTGGGGCAGCCTTTAGCAGCTGGGGGCAATTGAGAGCTTATGAGGAGTTTGAGGATGTCTGTAGCCTGGAGTGAGAATGAGCAGGACTGTATTAGGCGGGGCTGGATGGCAGGCAGAGGGAGCCTGTGGAGGGTGTGAGATCCCGTGCTGAGGCCCTGGGGTATATCACAGCTCAAAGCTGGTGGTTTTCAGTTGTCCTGAGAGAGGGCCTAGCAGAGGGACTGCTGGGGGGAAGGGCTGGAGGGTGGGGCAAGGGCGATCTTTGCTTCAGAGCAGCTCTGTTTTTATCTGTTTTGTTTTCTT... | AAGGGATGAGCAAAGGATTGGGGCAGCCTTTAGCAGCTGGGGGCAATTGAGAGCTTATGAGGAGTTTGAGGATGTCTGTAGCCTGGAGTGAGAATGAGCAGGACTGTATTAGGCGGGGCTGGATGGCAGGCAGAGGGAGCCTGTGGAGGGTGTGAGATCCCGTGCTGAGGCCCTGGGGTATATCACAGCTCAAAGCTGGTGGTTTTCAGTTGTCCTGAGAGAGGGCCTAGCAGAGGGACTGCTGGGGGGAAGGGCTGGAGGGTGGGGCAAGGGCGATCTTTGCTTCAGAGCAGCTCTGTTTTTATCTGTTTTGTTTTCTT... |
Task1_train_32682 | A mutation found on Chromosome 1 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | ACTGATAAGAAGTAGCCTGAAATTTTTAGATTTTCTACACATGGGGCATCATGAGGTTACCCAGGATTACGAGTGCCTTTACCTGGTTGCCTGCTCATCTGGGAAGTGTGTGCCCCCTCAGCAGGGGTTATATCTAGTTTATCTGTATTTCTCTAGAATTCTTTGCTTGTAGTGTGTTCAATTAATGTTTGTTGAGTACATAAATGAATGATATATCTCTGTTGTTTACATTGTCTGGAATACTCTTCTCTTAACTTCCTCACCTGCCCAACTCCCACCTTATAAAGTAAGCTTAGGCGGGGCGTGTTGGCTCACGCCTG... | ACTGATAAGAAGTAGCCTGAAATTTTTAGATTTTCTACACATGGGGCATCATGAGGTTACCCAGGATTACGAGTGCCTTTACCTGGTTGCCTGCTCATCTGGGAAGTGTGTGCCCCCTCAGCAGGGGTTATATCTAGTTTATCTGTATTTCTCTAGAATTCTTTGCTTGTAGTGTGTTCAATTAATGTTTGTTGAGTACATAAATGAATGATATATCTCTGTTGTTTACATTGTCTGGAATACTCTTCTCTTAACTTCCTCACCTGCCCAACTCCCACCTTATAAAGTAAGCTTAGGCGGGGCGTGTTGGCTCACGCCTG... |
Task1_train_32683 | Given a variant located on Chromosome 1, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GTATATAAGCTGTGAGAATCCCAGAGCCCTAAAGAATTGTAAGTGCAATAAGAAGCCAAATTCTGAGTTGGTTAACAAACATGGATTAAGTTGCTGCTGGGGAATGTAAAGAATTCTTTTGTTTGAGATCATGGAATGCTATATGAAATTGTACCCACATGGATGACAAACAACCAGTACGTCTTAACGGATTCCTATAAAAAGAATTCTACTTTGATAAAATCAATTTTGTGAAAAGCAGAAAGTTTTCATATAGTAAATTAGAATAGTGATTCTTATACTTTTTTTAGAGCATTGGACTACTTTAGAAATCAGATGAA... | GTATATAAGCTGTGAGAATCCCAGAGCCCTAAAGAATTGTAAGTGCAATAAGAAGCCAAATTCTGAGTTGGTTAACAAACATGGATTAAGTTGCTGCTGGGGAATGTAAAGAATTCTTTTGTTTGAGATCATGGAATGCTATATGAAATTGTACCCACATGGATGACAAACAACCAGTACGTCTTAACGGATTCCTATAAAAAGAATTCTACTTTGATAAAATCAATTTTGTGAAAAGCAGAAAGTTTTCATATAGTAAATTAGAATAGTGATTCTTATACTTTTTTTAGAGCATTGGACTACTTTAGAAATCAGATGAA... |
Task1_train_32684 | This variant is present on Chromosome 1. Is the change likely to result in a pathogenic outcome? | Benign | TGATGCTGCACTGTTTAAAAACCAGAGTAGCTTTTCATAATTCACCTGAAAATTAAATGTAAAATAGAACATCCTCATTTAATTTATATGTAAGGAAAGAGGCCTGTTGAGATAAAATGTATTTGGCAAATTTTTACCATCAAACATTTAAAAAAACACTTAAAAATATAGTATCATAATTATTGGTGCTTTTTAGCAAGTATTCTTATTATTTTCCCTTCTGGACAAATGGTAAAATTGTACTTCCTGGTTGTCTTCTGGTTGGGTAAGGCCATGTGACTAGTTCTGGCCAATGAGTTATAACCAGAACCGAGACCCTG... | TGATGCTGCACTGTTTAAAAACCAGAGTAGCTTTTCATAATTCACCTGAAAATTAAATGTAAAATAGAACATCCTCATTTAATTTATATGTAAGGAAAGAGGCCTGTTGAGATAAAATGTATTTGGCAAATTTTTACCATCAAACATTTAAAAAAACACTTAAAAATATAGTATCATAATTATTGGTGCTTTTTAGCAAGTATTCTTATTATTTTCCCTTCTGGACAAATGGTAAAATTGTACTTCCTGGTTGTCTTCTGGTTGGGTAAGGCCATGTGACTAGTTCTGGCCAATGAGTTATAACCAGAACCGAGACCCTG... |
Task1_train_32685 | This mutation occurs on Chromosome 1. Does this change lead to a known medical condition, or is it benign? | Benign | CTCATTTTGATAAATTATTATTTACCTTCTGTGTATGAAATATACATACATATAAAAGAATGTATATAATATCTGTACACATTTTAAATGATAATTAAAACAATAATTATTTGCAAGACCAACTTGGGCAACAGAGTGGGTCTCTATCTCAACAAAACAAAACAATAATTACCAGTGTGTAATACATACCACCTAGCTTAAGAAATATAACATTATGTATCTTTTCTTTCAACTCATCTGGAATCTTGACTTATTTATTTATTTATTTTATTTTTATGAGGTAGAGGCTTGCTCTGTCGCCCAAGCTGGAGTGCAGTGGC... | CTCATTTTGATAAATTATTATTTACCTTCTGTGTATGAAATATACATACATATAAAAGAATGTATATAATATCTGTACACATTTTAAATGATAATTAAAACAATAATTATTTGCAAGACCAACTTGGGCAACAGAGTGGGTCTCTATCTCAACAAAACAAAACAATAATTACCAGTGTGTAATACATACCACCTAGCTTAAGAAATATAACATTATGTATCTTTTCTTTCAACTCATCTGGAATCTTGACTTATTTATTTATTTATTTTATTTTTATGAGGTAGAGGCTTGCTCTGTCGCCCAAGCTGGAGTGCAGTGGC... |
Task1_train_32686 | This sequence variant lies on Chromosome 1. Is it clinically significant, and what condition might it cause if any? | Benign | AAATAAATAAAATAAAACAAAACAGACAAAAAAAAACTGAAACAAAAACAAAAGGAAAGAGAAATGATTATGGTGGAAAAGGGTGGAAGGCCACTGATTATCATCACCTGAGATGTCATTCTGTGTATTCTGGGAAGTTGTTGCCTTTCTCTACTTGGAACAGTATGAGTGGAAGTTTTCTATTTGAAATATCAGAACCTTTAAAAAGTTTCTCCAGCCGGTCTTGGTGGCTCATGCCTGTAATCCGAGCACTTTGGGAGGATGAGGTGGGTGGATCACATGAGGCCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGA... | AAATAAATAAAATAAAACAAAACAGACAAAAAAAAACTGAAACAAAAACAAAAGGAAAGAGAAATGATTATGGTGGAAAAGGGTGGAAGGCCACTGATTATCATCACCTGAGATGTCATTCTGTGTATTCTGGGAAGTTGTTGCCTTTCTCTACTTGGAACAGTATGAGTGGAAGTTTTCTATTTGAAATATCAGAACCTTTAAAAAGTTTCTCCAGCCGGTCTTGGTGGCTCATGCCTGTAATCCGAGCACTTTGGGAGGATGAGGTGGGTGGATCACATGAGGCCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGA... |
Task1_train_32687 | Chromosome 1 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TGCGTGCTGCGGACTGGGCTTGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCTGATGGCTCACTTGAGCCCAGGAGTTCAAGACCAGCTTGGGCAACATGGTGAAACACTGTCTCTACAAAAAATAAAAAAAAATTGTAGCCGCAGCTACTCGGGAGGCTGAGGTGGGATCGCTTGAACTGGGGAGGCAGAGGCTGCAGTGAGCCGTGATTGTGCCACTGCACACCAACCTGCAACCTGGGCAACAGAGCCAGATCCTGTTTCAAAAAAAAAAAAAAAAAGCCTGGTGTGTCCAGACTTTTATTTTCT... | TGCGTGCTGCGGACTGGGCTTGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCTGATGGCTCACTTGAGCCCAGGAGTTCAAGACCAGCTTGGGCAACATGGTGAAACACTGTCTCTACAAAAAATAAAAAAAAATTGTAGCCGCAGCTACTCGGGAGGCTGAGGTGGGATCGCTTGAACTGGGGAGGCAGAGGCTGCAGTGAGCCGTGATTGTGCCACTGCACACCAACCTGCAACCTGGGCAACAGAGCCAGATCCTGTTTCAAAAAAAAAAAAAAAAAGCCTGGTGTGTCCAGACTTTTATTTTCT... |
Task1_train_32688 | A mutation on Chromosome 1 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GTGACAGAGTGAGACTCTGTCTCAACGAATGAACAAACCAATGAAAGAAAGAAAGATAAGAAAGAGAGAGAGAGGGAGGGAAGGAAGGGAGGGAGGGAGGGGAGGGGAGGGGAGGGAAGAGGGGAGGGGAAGGTAGAGAGGAGGGGAGGGGAGGGAAGGCAGCGTAAACATTGTGAGTGGCAGCTGACATTCTGTCTCATCCCAAAGCTTCTATTTAGCATCAGCTAGTTTTTCTATGGGAGAAAGTAGTAGTGTGGGCAGATAGTTTCTGACTTGTCAGGGAGGCAAAGTGTTTTGTTTAAGATTCTTCAGGACAAGGA... | GTGACAGAGTGAGACTCTGTCTCAACGAATGAACAAACCAATGAAAGAAAGAAAGATAAGAAAGAGAGAGAGAGGGAGGGAAGGAAGGGAGGGAGGGAGGGGAGGGGAGGGGAGGGAAGAGGGGAGGGGAAGGTAGAGAGGAGGGGAGGGGAGGGAAGGCAGCGTAAACATTGTGAGTGGCAGCTGACATTCTGTCTCATCCCAAAGCTTCTATTTAGCATCAGCTAGTTTTTCTATGGGAGAAAGTAGTAGTGTGGGCAGATAGTTTCTGACTTGTCAGGGAGGCAAAGTGTTTTGTTTAAGATTCTTCAGGACAAGGA... |
Task1_train_32689 | Chromosome 1 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TTCAGTGACCAGCAGTCGTAATGGTTGGGAATTTCAAAAATAATTGTAGTTGTTGAATATTTGTTGTGTTAACTTTATTTCTCCTGTTATGCTGTGTGAGCATCTTTACTGTAATGCATGTCTTACATGTCTCTATTCATTCAAGTACCCACACAGCATCTTGTTCTTGGTTGCCGACCAGCAAAAATGCCTTGTATTTATTCACTTCAATGTTAATATGACTTAACTCTTTTCCTATATAGTTAACAGTTTTGTGATCTTGCAAGTCCTTCATTTTACTGTATTTTGCTAAATGTGTTCATTATTATTAGTAACAAGCT... | TTCAGTGACCAGCAGTCGTAATGGTTGGGAATTTCAAAAATAATTGTAGTTGTTGAATATTTGTTGTGTTAACTTTATTTCTCCTGTTATGCTGTGTGAGCATCTTTACTGTAATGCATGTCTTACATGTCTCTATTCATTCAAGTACCCACACAGCATCTTGTTCTTGGTTGCCGACCAGCAAAAATGCCTTGTATTTATTCACTTCAATGTTAATATGACTTAACTCTTTTCCTATATAGTTAACAGTTTTGTGATCTTGCAAGTCCTTCATTTTACTGTATTTTGCTAAATGTGTTCATTATTATTAGTAACAAGCT... |
Task1_train_32690 | This genomic variant is located on Chromosome 1. Can you determine its pathogenicity and name any linked disease? | Benign | CAAAAATAATTGTAGTTGTTGAATATTTGTTGTGTTAACTTTATTTCTCCTGTTATGCTGTGTGAGCATCTTTACTGTAATGCATGTCTTACATGTCTCTATTCATTCAAGTACCCACACAGCATCTTGTTCTTGGTTGCCGACCAGCAAAAATGCCTTGTATTTATTCACTTCAATGTTAATATGACTTAACTCTTTTCCTATATAGTTAACAGTTTTGTGATCTTGCAAGTCCTTCATTTTACTGTATTTTGCTAAATGTGTTCATTATTATTAGTAACAAGCTTTGTTCAGTGAGTGTTCTTTAAGATTCTCTTCAA... | CAAAAATAATTGTAGTTGTTGAATATTTGTTGTGTTAACTTTATTTCTCCTGTTATGCTGTGTGAGCATCTTTACTGTAATGCATGTCTTACATGTCTCTATTCATTCAAGTACCCACACAGCATCTTGTTCTTGGTTGCCGACCAGCAAAAATGCCTTGTATTTATTCACTTCAATGTTAATATGACTTAACTCTTTTCCTATATAGTTAACAGTTTTGTGATCTTGCAAGTCCTTCATTTTACTGTATTTTGCTAAATGTGTTCATTATTATTAGTAACAAGCTTTGTTCAGTGAGTGTTCTTTAAGATTCTCTTCAA... |
Task1_train_32691 | A variant affecting Chromosome 1 has been observed. Determine if it's benign or associated with disease. | Benign | CTGTGGAACCATATGGTGAATGAGCGGGATAAAAAAGGTCTATTTTATTTGAGATGCGTGTAAGACATCTAGTGGAGATATAAAGTAACAGTTGGGTACACAGGTCCTAGTCCTAAGCTCAAAAGATTTAGGCTAAATATGTGAATTTGGAAGACATCCATATATACAATAGTCTTTGAATTTAAGGGAAGGGAATAATTCACCTAGTTAGAGGTCATTGAACTCACATTGGAGGGGAAGGATGGGTGGGGTATAAATTAAATAAAGAATACAAAAATTAGCCAGGTGTGGTGGCACATGCCTGTAATCCCAGCTACTCC... | CTGTGGAACCATATGGTGAATGAGCGGGATAAAAAAGGTCTATTTTATTTGAGATGCGTGTAAGACATCTAGTGGAGATATAAAGTAACAGTTGGGTACACAGGTCCTAGTCCTAAGCTCAAAAGATTTAGGCTAAATATGTGAATTTGGAAGACATCCATATATACAATAGTCTTTGAATTTAAGGGAAGGGAATAATTCACCTAGTTAGAGGTCATTGAACTCACATTGGAGGGGAAGGATGGGTGGGGTATAAATTAAATAAAGAATACAAAAATTAGCCAGGTGTGGTGGCACATGCCTGTAATCCCAGCTACTCC... |
Task1_train_32692 | This genomic variant is located on Chromosome 1. Can you determine its pathogenicity and name any linked disease? | Benign | TTTATGCCACTGGTCCTTAGTCTTTAGAATGTTAGAATTAAAAAAGCCTTGGGGGCCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCTGGTGGATCACCTAAGGTCAAGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGCTGATCCCTGTAATCCCAGCTGCTCGGGAGTCTGAGTCTGGAGAATTGCTTGAAACCGGAAAGCGGAGGCTGCAATGAGCCGGGATCGCACCACTATACTCCAGCCTGGGTGACAGA... | TTTATGCCACTGGTCCTTAGTCTTTAGAATGTTAGAATTAAAAAAGCCTTGGGGGCCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCTGGTGGATCACCTAAGGTCAAGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGCTGATCCCTGTAATCCCAGCTGCTCGGGAGTCTGAGTCTGGAGAATTGCTTGAAACCGGAAAGCGGAGGCTGCAATGAGCCGGGATCGCACCACTATACTCCAGCCTGGGTGACAGA... |
Task1_train_32693 | This sequence variant lies on Chromosome 1. Is it clinically significant, and what condition might it cause if any? | Benign | AGGGTAGGCCTTAATTTAGGAAAAACAGCAACTAGCCTCCATCCCCAGGTGCAAGTGAGAGAAGACCTCTAGTCCCAGCCGGGTACAGTGGCTTACTCTGGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGCAGATCATGAGGTCAGGAGATAGATACCATCCTGGCTAACACGGTGAAACCCCATCTCTACTAAAAATACAAAAAAATTAGCCAGGTGTGGTGGCACGCACCTGTAGTCCCAGCTACTCGGGAGGCGGAGGCAGGAGAATCAGTTGAATCCAGGAGGCAGAGGTTGTAGTGAGCCAAGATCGCGCCAC... | AGGGTAGGCCTTAATTTAGGAAAAACAGCAACTAGCCTCCATCCCCAGGTGCAAGTGAGAGAAGACCTCTAGTCCCAGCCGGGTACAGTGGCTTACTCTGGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGCAGATCATGAGGTCAGGAGATAGATACCATCCTGGCTAACACGGTGAAACCCCATCTCTACTAAAAATACAAAAAAATTAGCCAGGTGTGGTGGCACGCACCTGTAGTCCCAGCTACTCGGGAGGCGGAGGCAGGAGAATCAGTTGAATCCAGGAGGCAGAGGTTGTAGTGAGCCAAGATCGCGCCAC... |
Task1_train_32694 | This mutation is located on Chromosome 1. Is it associated with a disease or is it a benign polymorphism? | Benign | CACTGAAACCTCTGCCTCCCAGGTTCAAGCAATTCTTATGCCTCAGCCTCCTGAGTAGCTGGTATTACAGGCACGTGCCACCATACCTGGCTAATTTTTGTATTTTTGTAGAGACGGGGTTTTGCCACGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAAATGATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTGCCTGCCTAACAATATTATTCTGTTGAGACAAGGTCTCACTCTGTCACCCAAGGTGTGGAGTGCAGGGGCACAATCACAGCTCACTGCAGTCTTAACTTTCC... | CACTGAAACCTCTGCCTCCCAGGTTCAAGCAATTCTTATGCCTCAGCCTCCTGAGTAGCTGGTATTACAGGCACGTGCCACCATACCTGGCTAATTTTTGTATTTTTGTAGAGACGGGGTTTTGCCACGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAAATGATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTGCCTGCCTAACAATATTATTCTGTTGAGACAAGGTCTCACTCTGTCACCCAAGGTGTGGAGTGCAGGGGCACAATCACAGCTCACTGCAGTCTTAACTTTCC... |
Task1_train_32695 | Given a variant located on Chromosome 1, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TATTACAGGCACGTGCCACCATACCTGGCTAATTTTTGTATTTTTGTAGAGACGGGGTTTTGCCACGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAAATGATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTGCCTGCCTAACAATATTATTCTGTTGAGACAAGGTCTCACTCTGTCACCCAAGGTGTGGAGTGCAGGGGCACAATCACAGCTCACTGCAGTCTTAACTTTCCAGGCTCAAGTCATCCTTGCATCTGAACCTCCCAAGTAGCTGGGACCACAGGCGTGTGTCACT... | TATTACAGGCACGTGCCACCATACCTGGCTAATTTTTGTATTTTTGTAGAGACGGGGTTTTGCCACGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAAATGATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTGCCTGCCTAACAATATTATTCTGTTGAGACAAGGTCTCACTCTGTCACCCAAGGTGTGGAGTGCAGGGGCACAATCACAGCTCACTGCAGTCTTAACTTTCCAGGCTCAAGTCATCCTTGCATCTGAACCTCCCAAGTAGCTGGGACCACAGGCGTGTGTCACT... |
Task1_train_32696 | A change on Chromosome 1 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GGCTTTTGCTCATGTTCTTGATCACCTTGTTGCCCTTGTTGAGACCCAAAGCCTTGGGGTCACACAGAGCAGTGGCTGCTGTTCTCCAATGGCTGCTGTGCTGGAAGGGGCTTTTTTTTTTTTTTTTGAGATAAAGTCTTGCTCTATTGCCCTGGTGGGGGTGCAGTGGCTCAATCTGGGCTCACTGCACCCTCCACCTCCCAGGCTCAAGTAATCCTCCTACTCCAGCCTCCTGATAGCTGGGACCACATGCATGCACTACCACACCCAGCTAATTTTTGTACTTTTTATAGAGACGAGGTTTTGCCATGTTGCCCATG... | GGCTTTTGCTCATGTTCTTGATCACCTTGTTGCCCTTGTTGAGACCCAAAGCCTTGGGGTCACACAGAGCAGTGGCTGCTGTTCTCCAATGGCTGCTGTGCTGGAAGGGGCTTTTTTTTTTTTTTTTGAGATAAAGTCTTGCTCTATTGCCCTGGTGGGGGTGCAGTGGCTCAATCTGGGCTCACTGCACCCTCCACCTCCCAGGCTCAAGTAATCCTCCTACTCCAGCCTCCTGATAGCTGGGACCACATGCATGCACTACCACACCCAGCTAATTTTTGTACTTTTTATAGAGACGAGGTTTTGCCATGTTGCCCATG... |
Task1_train_32697 | A variant on Chromosome 1 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | CCTCTTGCAGCCCACTGCCTTCTCAACCATCCAGGCTTGACAGAGAGCTCCAACTCACCTCACCAGTCCGGCACTACCCTCCCAATGGCTTTTTTTTTTTTTTTTTTTTTTGAGACAGGGTCTCTCTCTGTTGCCCAGGCTGGAGTGCAATGGCACTATCTCAGCTCACTGAAACCCCCACCCACCCCATGCTCAAGTTATTCTCCTGCTTCAGCCTCCTGAGTAGCTAGGATTACAGGCATGCGTCACTACCACCCAGCTAATTTTTGTATTTTTAATAGAGAGAGGGTTTCCCCATGTTGGCCAGGCTGGTCTTGAAC... | CCTCTTGCAGCCCACTGCCTTCTCAACCATCCAGGCTTGACAGAGAGCTCCAACTCACCTCACCAGTCCGGCACTACCCTCCCAATGGCTTTTTTTTTTTTTTTTTTTTTTGAGACAGGGTCTCTCTCTGTTGCCCAGGCTGGAGTGCAATGGCACTATCTCAGCTCACTGAAACCCCCACCCACCCCATGCTCAAGTTATTCTCCTGCTTCAGCCTCCTGAGTAGCTAGGATTACAGGCATGCGTCACTACCACCCAGCTAATTTTTGTATTTTTAATAGAGAGAGGGTTTCCCCATGTTGGCCAGGCTGGTCTTGAAC... |
Task1_train_32698 | Here is a variant on Chromosome 1. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TTGTGGCTGAAACACTTTAATAAATCAGAGTATCTCCTTTATCCATGGGATCTTCAAGAAAATCTGGAGAAAGATCCTAATATTAAGGAACAGAGGGGTGGATTTTGTTTTTTGTTTTTGTCCGTTTGTTTGGTTGGTTGGTTTCTTTTGAGACAGAGTCTCGCTCTGTGGCCCAGGCTGGAGTGCAGTTGTATGATCTCAGCTTGCTGTAACCTCCACCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTATAGGCGCGGGCCACCACACCCAGCTAATTTTCGTACTTTAGTAGAGACA... | TTGTGGCTGAAACACTTTAATAAATCAGAGTATCTCCTTTATCCATGGGATCTTCAAGAAAATCTGGAGAAAGATCCTAATATTAAGGAACAGAGGGGTGGATTTTGTTTTTTGTTTTTGTCCGTTTGTTTGGTTGGTTGGTTTCTTTTGAGACAGAGTCTCGCTCTGTGGCCCAGGCTGGAGTGCAGTTGTATGATCTCAGCTTGCTGTAACCTCCACCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTATAGGCGCGGGCCACCACACCCAGCTAATTTTCGTACTTTAGTAGAGACA... |
Task1_train_32699 | Given this variant on Chromosome 1, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CACACTGTGCACTGTACACTCACACCACTGCCTCACACTGTGCACCGTACGCTCACACCAATGCACACCCACACCACTGCCTCACACTGCATGCTCACACCACTGAACATTCACACCACTGCCTCACACACACACCACTCACACCACTGCACACTCACACCACTGCCTCACACTGCACACTCACACCATTCACATCACTGCACACCCACACTACTGCCTCACACTGTAAACTGCACACTCACACCACTGCACACTCACACCACTGCCTGCCTCACACCACTGAATGGGACCAAAGTCACCCTGGCAGAGCTAACGTCTTA... | CACACTGTGCACTGTACACTCACACCACTGCCTCACACTGTGCACCGTACGCTCACACCAATGCACACCCACACCACTGCCTCACACTGCATGCTCACACCACTGAACATTCACACCACTGCCTCACACACACACCACTCACACCACTGCACACTCACACCACTGCCTCACACTGCACACTCACACCATTCACATCACTGCACACCCACACTACTGCCTCACACTGTAAACTGCACACTCACACCACTGCACACTCACACCACTGCCTGCCTCACACCACTGAATGGGACCAAAGTCACCCTGGCAGAGCTAACGTCTTA... |
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