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_45700 | This mutation is located on Chromosome 17. Is it associated with a disease or is it a benign polymorphism? | Benign | AGATTCCAGTATCCCCCTACCCCCCAAAAAAAGAAAACATACAAAATCCTGCCTTGGTCCCAGTCTTAGGTTTCAATTTATGGGGCAAGTCTGATTAGTTTTGTTTTCTGAGCCAGACAGAACAAACGACTTGAAAAGGATTTCGCTCAGTCACATGCAGTGCACCAGGCAGCGCATCCAGTTTTGCTAGACCAGAATTCAACGTGACAGCCTCCGAGGGACGGGGGAGGTTTCTTCCTCCAGTCTCCTGTGAATTCACCTAGTCGCTCAGGGAAGTCATTTTAGCGACACTAATAATTAACCTCTGAGGCTGCCTCGTA... | AGATTCCAGTATCCCCCTACCCCCCAAAAAAAGAAAACATACAAAATCCTGCCTTGGTCCCAGTCTTAGGTTTCAATTTATGGGGCAAGTCTGATTAGTTTTGTTTTCTGAGCCAGACAGAACAAACGACTTGAAAAGGATTTCGCTCAGTCACATGCAGTGCACCAGGCAGCGCATCCAGTTTTGCTAGACCAGAATTCAACGTGACAGCCTCCGAGGGACGGGGGAGGTTTCTTCCTCCAGTCTCCTGTGAATTCACCTAGTCGCTCAGGGAAGTCATTTTAGCGACACTAATAATTAACCTCTGAGGCTGCCTCGTA... |
Task1_train_45701 | This sequence change occurs on Chromosome 17. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GGAAGGGCACTGACTTCAATTGAATTCTCCTGTGGGGTGGGTTCTCTCTGGAGGGTGCCTTAGCGGGAGGACAGACACAAGCCTCAAGTCATCCTCACTGGCACCTATGTCATGGGGGCTGCCTGGCACGCGAACCCCCATACTGCCTTGTCCTTCAGAGCACCCATTCAGCTTCAGAGGACGTGCATTCACCCAGACAGTGGCAAATTATGCGAGTGGCCCTATTTAAACACCACTGAACCTATTCCTGTAGGTACCATGTGCTGAGAGCCGAAAGCCTTGTAGAAAGTTCTTTAAGCGCTGTGCCCCACAGGATTGAG... | GGAAGGGCACTGACTTCAATTGAATTCTCCTGTGGGGTGGGTTCTCTCTGGAGGGTGCCTTAGCGGGAGGACAGACACAAGCCTCAAGTCATCCTCACTGGCACCTATGTCATGGGGGCTGCCTGGCACGCGAACCCCCATACTGCCTTGTCCTTCAGAGCACCCATTCAGCTTCAGAGGACGTGCATTCACCCAGACAGTGGCAAATTATGCGAGTGGCCCTATTTAAACACCACTGAACCTATTCCTGTAGGTACCATGTGCTGAGAGCCGAAAGCCTTGTAGAAAGTTCTTTAAGCGCTGTGCCCCACAGGATTGAG... |
Task1_train_45702 | Given this context: Chromosome 17 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TTCCCCCAGCTTGTTCTTTGGAAATCTCTACATATATTTTGCCTGGCAAGGGAAAACTCAGATATCAGGTTTGTTTTATTCGCGTTGCTTTATTCAGATATGTTCAAAGCATAATAGGAGTTATATAGAAATACCCATTATTGCTTTATTCAAGCATCGTTCTCATGAACCCCGACACCTCAAGTTCTCGCAGATTTTAGCTTTTAGTAAGACTTTTCCTTGGTTTATATTATTATTATTATTTTGAGATGGAGTTTCACTCTTGTTACCCAGGCTGGAATGCAATGGTGCCATCTTGGCTCACCGCAACCTCCGCCTCC... | TTCCCCCAGCTTGTTCTTTGGAAATCTCTACATATATTTTGCCTGGCAAGGGAAAACTCAGATATCAGGTTTGTTTTATTCGCGTTGCTTTATTCAGATATGTTCAAAGCATAATAGGAGTTATATAGAAATACCCATTATTGCTTTATTCAAGCATCGTTCTCATGAACCCCGACACCTCAAGTTCTCGCAGATTTTAGCTTTTAGTAAGACTTTTCCTTGGTTTATATTATTATTATTATTTTGAGATGGAGTTTCACTCTTGTTACCCAGGCTGGAATGCAATGGTGCCATCTTGGCTCACCGCAACCTCCGCCTCC... |
Task1_train_45703 | Here is a variant on Chromosome 17. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GACCCCCTCCGTGAGCCTTCCTGGGCATCTCTGCCTCTCTCTCCTCCTTTTCTTCTGCCCGCCACATCCCCCCTGCTCCCATTCATGCCTGTTCTTCAGAGCCAGGAGCCCTGTGTCTTTAAGGAAATCGCAGCTTCTCCTGTTTTGCAGCCCTAGCCTGGCCGGCATTTCCAAGGTGTGTGAGTGGTCCCGCCCCAGCTCCTGTGGCCTCCCTTCTGACCTCAGGCGGGTTCACCTGGCAGGGGAGCCCAGCCAGGGGGTGACTTATATCAGGGTGGGAACGTGGCAGCAGTGGCTGGGCCAGCCAGAGCCAGGGAAGA... | GACCCCCTCCGTGAGCCTTCCTGGGCATCTCTGCCTCTCTCTCCTCCTTTTCTTCTGCCCGCCACATCCCCCCTGCTCCCATTCATGCCTGTTCTTCAGAGCCAGGAGCCCTGTGTCTTTAAGGAAATCGCAGCTTCTCCTGTTTTGCAGCCCTAGCCTGGCCGGCATTTCCAAGGTGTGTGAGTGGTCCCGCCCCAGCTCCTGTGGCCTCCCTTCTGACCTCAGGCGGGTTCACCTGGCAGGGGAGCCCAGCCAGGGGGTGACTTATATCAGGGTGGGAACGTGGCAGCAGTGGCTGGGCCAGCCAGAGCCAGGGAAGA... |
Task1_train_45704 | This mutation on Chromosome 17 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TGTGACTATTAGATATTTATTTATTTATTTATTTTTGAGACAAAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAATGGTGCAGTCTCAGCTCACTGCAACCTCCACCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACCTGCCACCACGCCTAGCTAATTTTTTTTGTATTAGTAGAGCCGGGTTTCACCACGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAGGCGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGTGCCGGGCTAAC... | TGTGACTATTAGATATTTATTTATTTATTTATTTTTGAGACAAAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAATGGTGCAGTCTCAGCTCACTGCAACCTCCACCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACCTGCCACCACGCCTAGCTAATTTTTTTTGTATTAGTAGAGCCGGGTTTCACCACGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAGGCGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGTGCCGGGCTAAC... |
Task1_train_45705 | Chromosome 17 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TACAGGCACCTGCCACCACGCCTAGCTAATTTTTTTTGTATTAGTAGAGCCGGGTTTCACCACGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAGGCGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGTGCCGGGCTAACTATTAGATATTTAGACAGACAACCTGTGGCCTCTGTTTGGGGGTTTGTGCCTGTGGGGGCAGGGTACTTTACAAATGTCATCTCATTCCCGCTGACTGGGAGATGCCCCTGTGTTCCTCTGCATGAATGTCCCATGTCTTGGGCAGGATACAGGCA... | TACAGGCACCTGCCACCACGCCTAGCTAATTTTTTTTGTATTAGTAGAGCCGGGTTTCACCACGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAGGCGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGTGCCGGGCTAACTATTAGATATTTAGACAGACAACCTGTGGCCTCTGTTTGGGGGTTTGTGCCTGTGGGGGCAGGGTACTTTACAAATGTCATCTCATTCCCGCTGACTGGGAGATGCCCCTGTGTTCCTCTGCATGAATGTCCCATGTCTTGGGCAGGATACAGGCA... |
Task1_train_45706 | A variant affecting Chromosome 17 has been observed. Determine if it's benign or associated with disease. | Benign | CTGGAGTCCACACGGCTCCTTGCCCAGCTTCTGGTGGAGGTTGAGCTTAGTGACCCAGGATTTCGTCTGTGTCCACCAAGAAGGAGAGGTGCCTGTGGCTTAGAGAGGGCGCCCACAGGAGTGCCTTGCCCAGGAAGCTGGCAGCTGAGGCGGCCAGGGTTAGGGGGTTGGGCTTCCTCTTCCCCTCCCCAGTGCCTGAGTGCATTTGGAGGAAGAGAGACGGGTGAGGGGAAGGCACTGAAATTGGTCCTGGAGCGCTATTATTGGGGGCTGGGGACCAGCTGTCATCCCTTTTCCTGTGGGCAGGGGAGGCAGTGGTG... | CTGGAGTCCACACGGCTCCTTGCCCAGCTTCTGGTGGAGGTTGAGCTTAGTGACCCAGGATTTCGTCTGTGTCCACCAAGAAGGAGAGGTGCCTGTGGCTTAGAGAGGGCGCCCACAGGAGTGCCTTGCCCAGGAAGCTGGCAGCTGAGGCGGCCAGGGTTAGGGGGTTGGGCTTCCTCTTCCCCTCCCCAGTGCCTGAGTGCATTTGGAGGAAGAGAGACGGGTGAGGGGAAGGCACTGAAATTGGTCCTGGAGCGCTATTATTGGGGGCTGGGGACCAGCTGTCATCCCTTTTCCTGTGGGCAGGGGAGGCAGTGGTG... |
Task1_train_45707 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | CAGGGCAGGCTCATGCAGGGGTGTAGGACAGGGTGGAGTTGAGACCCCTAGAAGGGCTGTCACATTCTGGTGGCTCCTGCTTGAGGAATTGCAGGCTGCCTGGATATGCCCAGCAGAGGCCGAGGGCTTGGGGAAGGGAGGAGGGACGTATGCCTCCTGAGGCTTGCATTGGAGCCCATGGTCTGGTCCTCCTCCCCCAGGAGGGATGGTTGTGGCAGAGGGAGGGGAACATGAGGAGCACCTTAGCCTGCAGGACAAAATTCTCAGGGCACTGGGAAGGGGTGCCTGGACCAGGGGGCTGTGTGATAGCTGCACACGGT... | CAGGGCAGGCTCATGCAGGGGTGTAGGACAGGGTGGAGTTGAGACCCCTAGAAGGGCTGTCACATTCTGGTGGCTCCTGCTTGAGGAATTGCAGGCTGCCTGGATATGCCCAGCAGAGGCCGAGGGCTTGGGGAAGGGAGGAGGGACGTATGCCTCCTGAGGCTTGCATTGGAGCCCATGGTCTGGTCCTCCTCCCCCAGGAGGGATGGTTGTGGCAGAGGGAGGGGAACATGAGGAGCACCTTAGCCTGCAGGACAAAATTCTCAGGGCACTGGGAAGGGGTGCCTGGACCAGGGGGCTGTGTGATAGCTGCACACGGT... |
Task1_train_45708 | Chromosome 17 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GACCACTCTGAGATGGCCACCAGCTCGAGCCCGAGGGCACTTGTGGGTGCCCGTGGTCTCCTGCCCAGTCTCCCTGAGAAGTGGCCACTGTCCCGAGCTTGGGCTTGTATGTATTGTGTGAAGTGCACATGTCCCTGAGCAATGTTTAGCATTGCTGATTCTTGAGCTTGTGAATGGTCGTCCACAGTACGTAGCCCCTGTGTGTGTCCCTGTGTGTGTGTGCTCTGAGCGCACACAAGGTGGATGGGGCCGTGGGGGTAACACCCTGTGGGCCACAGGTTTTCTTTAAAATCCCAGCTCCGATTCCTGCTTCATCCCAT... | GACCACTCTGAGATGGCCACCAGCTCGAGCCCGAGGGCACTTGTGGGTGCCCGTGGTCTCCTGCCCAGTCTCCCTGAGAAGTGGCCACTGTCCCGAGCTTGGGCTTGTATGTATTGTGTGAAGTGCACATGTCCCTGAGCAATGTTTAGCATTGCTGATTCTTGAGCTTGTGAATGGTCGTCCACAGTACGTAGCCCCTGTGTGTGTCCCTGTGTGTGTGTGCTCTGAGCGCACACAAGGTGGATGGGGCCGTGGGGGTAACACCCTGTGGGCCACAGGTTTTCTTTAAAATCCCAGCTCCGATTCCTGCTTCATCCCAT... |
Task1_train_45709 | A change on Chromosome 17 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | ATTGCCTGGTTTCATAACCTCTTCTGTGCCTGTAGATAATGCAGTTGGCCCTTGAACAGTTTGGGATTAGGGTTACCAAAAGTATAACTTAGGACTTCCCAAAAACTTAACTACTTGACCAGAAGCCTTATTGATAGCAGTCAGTTAACACATACTTTTTATGCCTTCAGAGTTTTATACAATAAGATAAGCTAGAGAACAGAAGACATTATTAAGAAAATTGTAAAGACTGGGTACGGTAACTCACATCTGTAATCCCAGCACTTTGGGAGGCTGAAGCGGGGGGATCACTTGAGGTCAGGAGTTCGAGACCAGCCTGG... | ATTGCCTGGTTTCATAACCTCTTCTGTGCCTGTAGATAATGCAGTTGGCCCTTGAACAGTTTGGGATTAGGGTTACCAAAAGTATAACTTAGGACTTCCCAAAAACTTAACTACTTGACCAGAAGCCTTATTGATAGCAGTCAGTTAACACATACTTTTTATGCCTTCAGAGTTTTATACAATAAGATAAGCTAGAGAACAGAAGACATTATTAAGAAAATTGTAAAGACTGGGTACGGTAACTCACATCTGTAATCCCAGCACTTTGGGAGGCTGAAGCGGGGGGATCACTTGAGGTCAGGAGTTCGAGACCAGCCTGG... |
Task1_train_45710 | This mutation on Chromosome 17 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | CACCACCAGCCCTCTACACCAGTCTCATCCAACATAGCACCCACCAGCCACATCTGCCTAGAAGAGGGGGCAGGGCTGCATTCACCGCGGACTTGGCTGGCTGCCTCCCAGCGAGACATGGACCAGAAGATGCTGGGCTCACCTCAGGGCCTTTGCACTGCTGGTCCCAATGACCAAAACATCTTCCCTGCTTCCTTATCCATCCCCACTCTTATCTAACCTTCCCCTCTCAGGGCAAGTGCCGCCTCCCCTGGGAAGCAGCCTGACTCCTTCCCCAGTGCTCCCATAACACTGGGGAAACACCACTAAGCCTCATGGAT... | CACCACCAGCCCTCTACACCAGTCTCATCCAACATAGCACCCACCAGCCACATCTGCCTAGAAGAGGGGGCAGGGCTGCATTCACCGCGGACTTGGCTGGCTGCCTCCCAGCGAGACATGGACCAGAAGATGCTGGGCTCACCTCAGGGCCTTTGCACTGCTGGTCCCAATGACCAAAACATCTTCCCTGCTTCCTTATCCATCCCCACTCTTATCTAACCTTCCCCTCTCAGGGCAAGTGCCGCCTCCCCTGGGAAGCAGCCTGACTCCTTCCCCAGTGCTCCCATAACACTGGGGAAACACCACTAAGCCTCATGGAT... |
Task1_train_45711 | A mutation is present on Chromosome 17. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | AACACTGGGGAAACACCACTAAGCCTCATGGATTGTCCCAGCCCATTCAGTGGTCCATCTTCTCCCAGAGACAGCAAGCCCCCCTAGGACATTTACCATCCTGCCCTGAGCTGAGCACAGAGAATGTTTGTGGAATACGTAGATGCATGGGTGGATGGGTGGATGGATGGATGAATAAATGTGTGGGTGGATGGGTGGATGGATGAACGGATGGGTGGATGAATGGGTGGATAGATAAGGAGGTGGATGGATGTGCGAATGGATGGATGCGTGGATGAATGAGTGGGTGGATGGATGAATGGGTGGATGGGTGGGTTAAA... | AACACTGGGGAAACACCACTAAGCCTCATGGATTGTCCCAGCCCATTCAGTGGTCCATCTTCTCCCAGAGACAGCAAGCCCCCCTAGGACATTTACCATCCTGCCCTGAGCTGAGCACAGAGAATGTTTGTGGAATACGTAGATGCATGGGTGGATGGGTGGATGGATGGATGAATAAATGTGTGGGTGGATGGGTGGATGGATGAACGGATGGGTGGATGAATGGGTGGATAGATAAGGAGGTGGATGGATGTGCGAATGGATGGATGCGTGGATGAATGAGTGGGTGGATGGATGAATGGGTGGATGGGTGGGTTAAA... |
Task1_train_45712 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | GCTGAATGGGTAAATGGGTGGGTGAATTGAGTGGGTGGATGGGTGGGTGGATGGATGAATGGGTGGATGGGTGGGTAGGTAGATGGATGGGTAGATGGGTGGGTAAGTGGATAGTTGGATAGGTGAGTGGATGAGAGCAGACAGGTAGATGGACAGAAGGAAGAAAGGAAGAGGGAAGAATCAATGAATGGGTCGAAAGATGAATGGATGGATGAGTGGAGCTCGGAGCCTGGGTCATGAGGTGGAGGCATTACCTGTACACCAGGGTGATGCAGGTGATAAAGAAGCTCACGCCCACAGTGGAGAGGTAGGCCAGGGGC... | GCTGAATGGGTAAATGGGTGGGTGAATTGAGTGGGTGGATGGGTGGGTGGATGGATGAATGGGTGGATGGGTGGGTAGGTAGATGGATGGGTAGATGGGTGGGTAAGTGGATAGTTGGATAGGTGAGTGGATGAGAGCAGACAGGTAGATGGACAGAAGGAAGAAAGGAAGAGGGAAGAATCAATGAATGGGTCGAAAGATGAATGGATGGATGAGTGGAGCTCGGAGCCTGGGTCATGAGGTGGAGGCATTACCTGTACACCAGGGTGATGCAGGTGATAAAGAAGCTCACGCCCACAGTGGAGAGGTAGGCCAGGGGC... |
Task1_train_45713 | A mutation on Chromosome 17 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CCAAGGACAGAGAATTGGCAAAGATATGTCTTAAACATCTAGCCTGGGAGAGCATGAATGGAGCCAATTCCTGAGCACTTACTACCGGCCAGGTGCTAGGCCTGGGTCTTGGCACAACCATAACGCCAATGACAGGGGCTGGAAGTACAGCAGTAACACCAAGAGTATCTGGAAACCCAGCAGCCAGGTTCTGGGGAGCCCACCATCCTGTCATTATCACACCCTCCAGGGTGAGGCCGGCAGATAAAGAGTTTGGCCCCTGTGCCCCCACCGTTCCCATCCCCACCCATGTCAGGCTCCCAGCTCAGGCCTCGAGGTCA... | CCAAGGACAGAGAATTGGCAAAGATATGTCTTAAACATCTAGCCTGGGAGAGCATGAATGGAGCCAATTCCTGAGCACTTACTACCGGCCAGGTGCTAGGCCTGGGTCTTGGCACAACCATAACGCCAATGACAGGGGCTGGAAGTACAGCAGTAACACCAAGAGTATCTGGAAACCCAGCAGCCAGGTTCTGGGGAGCCCACCATCCTGTCATTATCACACCCTCCAGGGTGAGGCCGGCAGATAAAGAGTTTGGCCCCTGTGCCCCCACCGTTCCCATCCCCACCCATGTCAGGCTCCCAGCTCAGGCCTCGAGGTCA... |
Task1_train_45714 | This alteration occurs on Chromosome 17. Is it associated with a disease or is it a benign variant? | Benign | GTCTAAGAGGACCTCTGCTCCTCCAGGGACATTTCGGCTCCTCAGGGGATGGTCTTACCTAGACAGACTGGCCTGGCCGGTGGTGGGGTTAGAGAGAGGCTGAGGCCACTGTGCCCAACATAGACTCATGGACACATGCCCGTGGTCCTCAGAGCCCAGCTGGTGTAGGCGGTGCCAGGGACAAAGGGGGAAAAGTGCCCCGGCCTCTGGGAGAAGCACTTCCCCACCCTCATCCTGGGAAGCCATCGAGTGGTCACCAATGGGGTTCCTGGGTTCCAGTCGTGGCTCTATTTCTCAAAGCCCTGTGACCGTGGGCACGT... | GTCTAAGAGGACCTCTGCTCCTCCAGGGACATTTCGGCTCCTCAGGGGATGGTCTTACCTAGACAGACTGGCCTGGCCGGTGGTGGGGTTAGAGAGAGGCTGAGGCCACTGTGCCCAACATAGACTCATGGACACATGCCCGTGGTCCTCAGAGCCCAGCTGGTGTAGGCGGTGCCAGGGACAAAGGGGGAAAAGTGCCCCGGCCTCTGGGAGAAGCACTTCCCCACCCTCATCCTGGGAAGCCATCGAGTGGTCACCAATGGGGTTCCTGGGTTCCAGTCGTGGCTCTATTTCTCAAAGCCCTGTGACCGTGGGCACGT... |
Task1_train_45715 | A variant affecting Chromosome 17 has been observed. Determine if it's benign or associated with disease. | Benign | TTAAAAAAAAAAGGAAAAGAAAAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGTGCATGCCTGGAGTCCCCACTACATGGTAGGCTGAGACAGGAGAATCGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCTGAGATCGTGCTACTGCACTCCATTCTGGACGACAGAGCAAGACTCTGTCTTTAAATAAATAAATAAAAGTGGGCCGGGCGCAGTGGCTCACATCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGCCAGACCACCTGAGGTCTCGAGTTCAAGACCAGTCTGGCCAACAT... | TTAAAAAAAAAAGGAAAAGAAAAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGTGCATGCCTGGAGTCCCCACTACATGGTAGGCTGAGACAGGAGAATCGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCTGAGATCGTGCTACTGCACTCCATTCTGGACGACAGAGCAAGACTCTGTCTTTAAATAAATAAATAAAAGTGGGCCGGGCGCAGTGGCTCACATCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGCCAGACCACCTGAGGTCTCGAGTTCAAGACCAGTCTGGCCAACAT... |
Task1_train_45716 | A variant was discovered on Chromosome 17. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TTGGAAAGACCATCTTTGTAGGTGTTATTAGCTAAAGTCAAGTCATTCTGGGTTAGGGTGGGCCCTAAATGCCATTGACTGCTATCCTGCTAAGAGACAGAAGAGGGAGGGACACACAGGGAGGGGACCACGTGAAGACGGAGGCAGAGACGGGAAGAGGCAGAGGTGACTGGAGTGACGTAGCCCCAGGCCTTGGAACGCCTGGAGCCACCAGGAGCTGCAGGAGGCAAAAGAGGCATTGGCAGAGTGTGGCAGTGTCCACACCTTAATTTCAGACTTCTGGCCTTTAGAACTGTGAGAGAATCACGTTCTACTGCTGT... | TTGGAAAGACCATCTTTGTAGGTGTTATTAGCTAAAGTCAAGTCATTCTGGGTTAGGGTGGGCCCTAAATGCCATTGACTGCTATCCTGCTAAGAGACAGAAGAGGGAGGGACACACAGGGAGGGGACCACGTGAAGACGGAGGCAGAGACGGGAAGAGGCAGAGGTGACTGGAGTGACGTAGCCCCAGGCCTTGGAACGCCTGGAGCCACCAGGAGCTGCAGGAGGCAAAAGAGGCATTGGCAGAGTGTGGCAGTGTCCACACCTTAATTTCAGACTTCTGGCCTTTAGAACTGTGAGAGAATCACGTTCTACTGCTGT... |
Task1_train_45717 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | ACTGCCACAAGCTGGGCACTCCTTGCAGGGCTGTGTCTCACAGCGCTGGAGAACGGAAGTCTCAAGTCAAATGTGGGCAGGGTTCCTAGGGAGGGTCCTTCCTGCCTTCTCCAGCTTCTGGTGGCCTTAGACAGCCCTTAGCTTGTGTCTGCATAGCTCCAGCCTCTGCCTCCATTCACATGTGATCCTGGTGTTCCTGGGTCTCAAATCTTCCTCTCTCTTTTTTTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTCACTCTAACCCAGACTGGAACGCAGTGGTGCGACCTCAGCTCACTGCAACTTCTGCCTCCCGG... | ACTGCCACAAGCTGGGCACTCCTTGCAGGGCTGTGTCTCACAGCGCTGGAGAACGGAAGTCTCAAGTCAAATGTGGGCAGGGTTCCTAGGGAGGGTCCTTCCTGCCTTCTCCAGCTTCTGGTGGCCTTAGACAGCCCTTAGCTTGTGTCTGCATAGCTCCAGCCTCTGCCTCCATTCACATGTGATCCTGGTGTTCCTGGGTCTCAAATCTTCCTCTCTCTTTTTTTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTCACTCTAACCCAGACTGGAACGCAGTGGTGCGACCTCAGCTCACTGCAACTTCTGCCTCCCGG... |
Task1_train_45718 | A mutation located on Chromosome 17 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CTGGCAGCCCCTTGTCCCCGTCCCTGTCAGGCACTGTCAGAGCTGTTCACCCCACACCTCCTGATGCCGCGGGGGCAGGGGTTCCAAATGTGTACAGAGGCTTCAGAGTCCGGGGAGAGAGAAGGGGATCCCAGCAGGCTGGAGGGTCCACAGGGCCCCCTCCGTTCCCCCCAGCTCCCTCCTCCGGAGCTGGGGCCAGCCTGGGGAGCTTCCCCTTCACAGCGCGAGGGCTGGCAGGGCAGGGGTGTGTGTGTGAGTGAGCATGTGTGTGCATCTGAATATGTGTGCATGTGCTGAACATGAACATGTGTGAGCACCTG... | CTGGCAGCCCCTTGTCCCCGTCCCTGTCAGGCACTGTCAGAGCTGTTCACCCCACACCTCCTGATGCCGCGGGGGCAGGGGTTCCAAATGTGTACAGAGGCTTCAGAGTCCGGGGAGAGAGAAGGGGATCCCAGCAGGCTGGAGGGTCCACAGGGCCCCCTCCGTTCCCCCCAGCTCCCTCCTCCGGAGCTGGGGCCAGCCTGGGGAGCTTCCCCTTCACAGCGCGAGGGCTGGCAGGGCAGGGGTGTGTGTGTGAGTGAGCATGTGTGTGCATCTGAATATGTGTGCATGTGCTGAACATGAACATGTGTGAGCACCTG... |
Task1_train_45719 | A mutation is present on Chromosome 17. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GGGGACGCCTCCCCTCCTGGCCTTAGGAAGCCCCTGCCAGAGTCAGAGGGGGCCACTGGGAGGGTCCAGTGGTGTCCACAGAGATGGGCGTCAGCCGCTTTTCCTGAGAAGACGAAGCACCACGTCACTGTCCTCCGGCAGACAAGTGCTGAAGGGCCCACCTGGACCAGAATTCTCACCTGAGCCCCCTTTCCTGCAGTGCTGCACCGTGCAGTCATTGTGGTCCTGCCCCTGAGCCTGGTCCTTCTCGTGTGTGGCTGGATCTGCGGCCTGCTCAGCTCCCTGGCCCAGAGCGTGTCTCTGCTGCTTTTCACCGGCTG... | GGGGACGCCTCCCCTCCTGGCCTTAGGAAGCCCCTGCCAGAGTCAGAGGGGGCCACTGGGAGGGTCCAGTGGTGTCCACAGAGATGGGCGTCAGCCGCTTTTCCTGAGAAGACGAAGCACCACGTCACTGTCCTCCGGCAGACAAGTGCTGAAGGGCCCACCTGGACCAGAATTCTCACCTGAGCCCCCTTTCCTGCAGTGCTGCACCGTGCAGTCATTGTGGTCCTGCCCCTGAGCCTGGTCCTTCTCGTGTGTGGCTGGATCTGCGGCCTGCTCAGCTCCCTGGCCCAGAGCGTGTCTCTGCTGCTTTTCACCGGCTG... |
Task1_train_45720 | This mutation on Chromosome 17 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GATTATGTCCTACAGCTTTTCCAGTTTCCAGGTCCCAGCCTATGTGGGTCAGCCAGGGAGCTGCATATTACAGATCAGAGATCACCTCTCCTGCCTTTCAGAATGCCACAAAGTTTTCCATTTTAAAATTAGCTGCAAAAAGTGTTCTTGGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGAAGGCCGAGTTGGGTGGATCACTTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACACGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGCGCACGCCTGTAATCCCAGC... | GATTATGTCCTACAGCTTTTCCAGTTTCCAGGTCCCAGCCTATGTGGGTCAGCCAGGGAGCTGCATATTACAGATCAGAGATCACCTCTCCTGCCTTTCAGAATGCCACAAAGTTTTCCATTTTAAAATTAGCTGCAAAAAGTGTTCTTGGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGAAGGCCGAGTTGGGTGGATCACTTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACACGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGCGCACGCCTGTAATCCCAGC... |
Task1_train_45721 | A variant was discovered on Chromosome 17. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CCATTTTAAAATTAGCTGCAAAAAGTGTTCTTGGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGAAGGCCGAGTTGGGTGGATCACTTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACACGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGCGCACGCCTGTAATCCCAGCTATTCCGGAGGCTGAGACAGGAAAATCTCTTGATCCCAGGAGGCAGAGGTTGCAGTGAGCCAAGATTGCGCCATTGCACTCCAGCCTGGGTGACAAGAGTGAAACCCTGCCTCAAAA... | CCATTTTAAAATTAGCTGCAAAAAGTGTTCTTGGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGAAGGCCGAGTTGGGTGGATCACTTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACACGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGCGCACGCCTGTAATCCCAGCTATTCCGGAGGCTGAGACAGGAAAATCTCTTGATCCCAGGAGGCAGAGGTTGCAGTGAGCCAAGATTGCGCCATTGCACTCCAGCCTGGGTGACAAGAGTGAAACCCTGCCTCAAAA... |
Task1_train_45722 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GGCTGCTGTGAGCTGCATGGCCCCATAGCACCGTGTGTACCCCACGCACTCATCACACTAGGGTGCTGCTTCCAGAACGTATCCTCGCGCCCCTCAGCAGGGTGCAGGCCAAGGCAGGAGGCGTGTGGTATTGATTGATTGGTTAATAGAACGGGGGACCTATTTTAAACATTTGTTTTTCTGCTTTTTCTTTTACTTTCACACTTTGACAAGGGTGTGTCCTTTAAAAGCTGGTTGGGAATTGTTAATGGGTGACTCTGATATTTCCATATAAGTAGTTTTTAAAAATGTATCAGGCATGGAAGCCACACATTCATGGA... | GGCTGCTGTGAGCTGCATGGCCCCATAGCACCGTGTGTACCCCACGCACTCATCACACTAGGGTGCTGCTTCCAGAACGTATCCTCGCGCCCCTCAGCAGGGTGCAGGCCAAGGCAGGAGGCGTGTGGTATTGATTGATTGGTTAATAGAACGGGGGACCTATTTTAAACATTTGTTTTTCTGCTTTTTCTTTTACTTTCACACTTTGACAAGGGTGTGTCCTTTAAAAGCTGGTTGGGAATTGTTAATGGGTGACTCTGATATTTCCATATAAGTAGTTTTTAAAAATGTATCAGGCATGGAAGCCACACATTCATGGA... |
Task1_train_45723 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CGGAGCCCACAGGGGAGAAACACAGGATCACCTGGGTGTGGGAGACACAGATGCGCTGCCTACTGGGACTGCAGTGCTGGGGCCTAATCCATCACTCTGCAGAAAGCTCTGCCAGAAAGCAACGCGCCCTGCCGGGCTCAGCCGCCCAGGGCCTGGGCAGCACAGTCCTGGTTCTGGGTTTGAAGGGCGGCCGCTGCATTGCCGTGGATAAATGCTCATCTGGCTTCATGCCTCTCGCTAGCAGTCCCAATCCCTCTGGAAGGGGCCCTTGCCTCTCTAAAAAAGGCCGGGCAAAGGAAGGAATGGGGAGTGGGCATCCA... | CGGAGCCCACAGGGGAGAAACACAGGATCACCTGGGTGTGGGAGACACAGATGCGCTGCCTACTGGGACTGCAGTGCTGGGGCCTAATCCATCACTCTGCAGAAAGCTCTGCCAGAAAGCAACGCGCCCTGCCGGGCTCAGCCGCCCAGGGCCTGGGCAGCACAGTCCTGGTTCTGGGTTTGAAGGGCGGCCGCTGCATTGCCGTGGATAAATGCTCATCTGGCTTCATGCCTCTCGCTAGCAGTCCCAATCCCTCTGGAAGGGGCCCTTGCCTCTCTAAAAAAGGCCGGGCAAAGGAAGGAATGGGGAGTGGGCATCCA... |
Task1_train_45724 | A variant found on Chromosome 17 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | TCAAAGAAAAGAAATAAGTAACAGTGAAAATGGTCAATTTTATACTATGTATATTTTACCACATATGCAAAAGGAAAGAAAAAAATCTTAAATGGAGACCCTAAAAGAGGCCCTGAATAAATATACTGCAGGCTTGGACTGGGAGCCTTAACAGGCAACCCCCTTTCAGAGTCATCCACAGCAGGATTTAAGGACAGGGCGAGAAGATGGTTTCATAGGAATTTTGCAAGAATAAATGAAAAGTTTTTTTTAAAGCATTTTACAGAGCAGTAGGAATAGCTCGTTATTTTTGAATATGCCATTTCCATGTATATATATGT... | TCAAAGAAAAGAAATAAGTAACAGTGAAAATGGTCAATTTTATACTATGTATATTTTACCACATATGCAAAAGGAAAGAAAAAAATCTTAAATGGAGACCCTAAAAGAGGCCCTGAATAAATATACTGCAGGCTTGGACTGGGAGCCTTAACAGGCAACCCCCTTTCAGAGTCATCCACAGCAGGATTTAAGGACAGGGCGAGAAGATGGTTTCATAGGAATTTTGCAAGAATAAATGAAAAGTTTTTTTTAAAGCATTTTACAGAGCAGTAGGAATAGCTCGTTATTTTTGAATATGCCATTTCCATGTATATATATGT... |
Task1_train_45725 | A mutation located on Chromosome 17 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CCCATGACCACACCCGGCTAATTTTTGTACTTTTAGTAGAGACAGGGTTTCACCATGTTGGTCAGGCTGGTCTCAAACTCCTGATCTCAGGTGATCAGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGAGTGAGCCGCTGCGCCCGGCCCTGGATGCCTTTTATGAACCACCAGGCTGAACCCTTCTCTGGATCACGTTTGCTCTGGAGACACACAGGTGAGTTTACACCCCCCAACCATGGCTGAGGCGAAGGAGGCCTGGGTGATGGGAAGCTAACTGTTCACTGTGCGTGTCTGCAGCCCGCAGAGAGCTGC... | CCCATGACCACACCCGGCTAATTTTTGTACTTTTAGTAGAGACAGGGTTTCACCATGTTGGTCAGGCTGGTCTCAAACTCCTGATCTCAGGTGATCAGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGAGTGAGCCGCTGCGCCCGGCCCTGGATGCCTTTTATGAACCACCAGGCTGAACCCTTCTCTGGATCACGTTTGCTCTGGAGACACACAGGTGAGTTTACACCCCCCAACCATGGCTGAGGCGAAGGAGGCCTGGGTGATGGGAAGCTAACTGTTCACTGTGCGTGTCTGCAGCCCGCAGAGAGCTGC... |
Task1_train_45726 | With a mutation on Chromosome 17, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GTTCCATCCCCCTTGCCTTCCCGTCTTGCAAGAGGCTGCTGCAGCCTGGAGCTCCGAGGTATCCCCTTCCCCTCCCTGGCCTCCTGTGAGCCGACGATGTCCTGTGCAGGCTCTAATGACTGATGGGACCGGGCCAATCCCCTGCTCCCCTCCCAAACCCACCTGGACACTGCTTGTACCCCACCCCATGCTGAACCATGAGGGAGGTGCTCACCCCTGTGCGGAGTCCCCAGTTCGGGGCAATCTTAACAACTGAAATTGAGAGAGGGTCACCTCCAGGGCAGGGGCTGGGGCAGGACATTTGGGGCTGCGTCTGTCCA... | GTTCCATCCCCCTTGCCTTCCCGTCTTGCAAGAGGCTGCTGCAGCCTGGAGCTCCGAGGTATCCCCTTCCCCTCCCTGGCCTCCTGTGAGCCGACGATGTCCTGTGCAGGCTCTAATGACTGATGGGACCGGGCCAATCCCCTGCTCCCCTCCCAAACCCACCTGGACACTGCTTGTACCCCACCCCATGCTGAACCATGAGGGAGGTGCTCACCCCTGTGCGGAGTCCCCAGTTCGGGGCAATCTTAACAACTGAAATTGAGAGAGGGTCACCTCCAGGGCAGGGGCTGGGGCAGGACATTTGGGGCTGCGTCTGTCCA... |
Task1_train_45727 | This variant is found on Chromosome 17. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GCGGGAATTATGCAACGGGGGATTTGAAAGGCATGTGCGTGGCTTGGGCTTTCCGTGGGTGGTTTTAGGCATCGTTCTTTTTGGAATATACTCCCCATCTTTGATCAACGTTGACTAAACATGACTAAGTCAACAAAAGGAACCAGCGAAGACTGCTCTGAGTCAGGACACAGAAACCAGGCCAGGAACCGCAGCCCTTCTAAGCCAAACATCCATTCTGGAAGATTTCTTTTTGGTGGGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGGATCACCCGAGGTCAGGAGTTCGAGACC... | GCGGGAATTATGCAACGGGGGATTTGAAAGGCATGTGCGTGGCTTGGGCTTTCCGTGGGTGGTTTTAGGCATCGTTCTTTTTGGAATATACTCCCCATCTTTGATCAACGTTGACTAAACATGACTAAGTCAACAAAAGGAACCAGCGAAGACTGCTCTGAGTCAGGACACAGAAACCAGGCCAGGAACCGCAGCCCTTCTAAGCCAAACATCCATTCTGGAAGATTTCTTTTTGGTGGGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGGATCACCCGAGGTCAGGAGTTCGAGACC... |
Task1_train_45728 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | AGAGCACCTTGAACAGACTAAGTGGTATTCCTTACTTAAAAAAATTTCTTTAAAAAAGGTGAGATGTGAGAGAGAATGAGAGGAGGAGGAAAAAGACGAAGGGAGGGGAAAAAAGAAAGGGGGGCAGTCAAAGGCGAGCCCCCACCCACATACAGAGAGAGGTGAACATATCCTGCTTTAGCGGAGGGACCCCACCTCGCGATCTCAGGGCCCTTCGGATGCCTCCACCCAACACCAGAAACCTTCTTGTCACATTCTTACAACCAAAGGGTGCCCAGAGCCTGCCCTCTTGTTGCCGGGGGCAGCTCCCTGCAGAATCC... | AGAGCACCTTGAACAGACTAAGTGGTATTCCTTACTTAAAAAAATTTCTTTAAAAAAGGTGAGATGTGAGAGAGAATGAGAGGAGGAGGAAAAAGACGAAGGGAGGGGAAAAAAGAAAGGGGGGCAGTCAAAGGCGAGCCCCCACCCACATACAGAGAGAGGTGAACATATCCTGCTTTAGCGGAGGGACCCCACCTCGCGATCTCAGGGCCCTTCGGATGCCTCCACCCAACACCAGAAACCTTCTTGTCACATTCTTACAACCAAAGGGTGCCCAGAGCCTGCCCTCTTGTTGCCGGGGGCAGCTCCCTGCAGAATCC... |
Task1_train_45729 | A mutation located on Chromosome 17 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | AACCGTGCTATGTTCTGAATGGCCCAGCTACATAGAGGGAGAGGAGGATTCACTTTTGAACCCAACTCTTCTAAATTCAACCATCACAGAAAAAAACTCAGGCTGGGAGTTCAGGGAGTCATTCCGTGAGAAGCTGTAGACAGAACAGCTTTGAATCGGAAGACCCACTGGCATTCACAGAATGTTTTAAAGTTCATGTGCACTGTAACCTCTCTCATGGGGCTGTTTCAGTCAAATGCTGTGACACATGAGGAAGCTTCAACCCCATCACCCAAGGGAGCAGACTCGGGGGTGGGGGGTGAAGGTTGGTAGGGTCCCAG... | AACCGTGCTATGTTCTGAATGGCCCAGCTACATAGAGGGAGAGGAGGATTCACTTTTGAACCCAACTCTTCTAAATTCAACCATCACAGAAAAAAACTCAGGCTGGGAGTTCAGGGAGTCATTCCGTGAGAAGCTGTAGACAGAACAGCTTTGAATCGGAAGACCCACTGGCATTCACAGAATGTTTTAAAGTTCATGTGCACTGTAACCTCTCTCATGGGGCTGTTTCAGTCAAATGCTGTGACACATGAGGAAGCTTCAACCCCATCACCCAAGGGAGCAGACTCGGGGGTGGGGGGTGAAGGTTGGTAGGGTCCCAG... |
Task1_train_45730 | This sequence variant lies on Chromosome 17. Is it clinically significant, and what condition might it cause if any? | Benign | AATTCCAGTAATCATGGACTTAACACACTATTCCAAACAGATGAAGGGGACAAGAGCACATGGATATAGAAAATGAAAACTGCATCATCAGTAGACCCATCCATGGACAGAGGAGCAAACCAACACCCTGGCAGTCTCAGCAGCCACCGCCAAGCATGCAGGAAACATTCACAAACGCTGGTCACCTATAATCACGGAGAAAACATCAGGAAGTTCCATGAAGTAGAAATATTATCAACACGCTCTGATCATAATGCAAGTAACATCAAAAGTCATCTACAGAAGCAAAAGACAAAAAGGCCCCTCCACCTGCAAATTAA... | AATTCCAGTAATCATGGACTTAACACACTATTCCAAACAGATGAAGGGGACAAGAGCACATGGATATAGAAAATGAAAACTGCATCATCAGTAGACCCATCCATGGACAGAGGAGCAAACCAACACCCTGGCAGTCTCAGCAGCCACCGCCAAGCATGCAGGAAACATTCACAAACGCTGGTCACCTATAATCACGGAGAAAACATCAGGAAGTTCCATGAAGTAGAAATATTATCAACACGCTCTGATCATAATGCAAGTAACATCAAAAGTCATCTACAGAAGCAAAAGACAAAAAGGCCCCTCCACCTGCAAATTAA... |
Task1_train_45731 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | ATTCCAGTAATCATGGACTTAACACACTATTCCAAACAGATGAAGGGGACAAGAGCACATGGATATAGAAAATGAAAACTGCATCATCAGTAGACCCATCCATGGACAGAGGAGCAAACCAACACCCTGGCAGTCTCAGCAGCCACCGCCAAGCATGCAGGAAACATTCACAAACGCTGGTCACCTATAATCACGGAGAAAACATCAGGAAGTTCCATGAAGTAGAAATATTATCAACACGCTCTGATCATAATGCAAGTAACATCAAAAGTCATCTACAGAAGCAAAAGACAAAAAGGCCCCTCCACCTGCAAATTAAA... | ATTCCAGTAATCATGGACTTAACACACTATTCCAAACAGATGAAGGGGACAAGAGCACATGGATATAGAAAATGAAAACTGCATCATCAGTAGACCCATCCATGGACAGAGGAGCAAACCAACACCCTGGCAGTCTCAGCAGCCACCGCCAAGCATGCAGGAAACATTCACAAACGCTGGTCACCTATAATCACGGAGAAAACATCAGGAAGTTCCATGAAGTAGAAATATTATCAACACGCTCTGATCATAATGCAAGTAACATCAAAAGTCATCTACAGAAGCAAAAGACAAAAAGGCCCCTCCACCTGCAAATTAAA... |
Task1_train_45732 | This mutation is located on Chromosome 17. Is it associated with a disease or is it a benign polymorphism? | Benign | CAGGTGTGAGCCACCGTGCCCAGCCAGTAGCAGTCACTTCTATAGCACTCCCTCTTTGCGGGCTGCTACTCCAGGCACTTGACTCACTCAGAATTTATCGGAGCCTCACGCAACTCTGTAAGGAAGACAGTCTCATTCTTCCATAGACCAGGGACATTCTCAAAAACTCACAGTTACTAAGGGGCAAACTGGGAAGCAAACCCTACAGGCCAGGCTCCTGAGCTGTGTTTTCAACTGCTCTGCTCCCTCCAGAATTCTACTTAGAGATTTTCTGCGATGAAAACATCCTGCATTCCTAGGATAAACATAAGTTGCTTACA... | CAGGTGTGAGCCACCGTGCCCAGCCAGTAGCAGTCACTTCTATAGCACTCCCTCTTTGCGGGCTGCTACTCCAGGCACTTGACTCACTCAGAATTTATCGGAGCCTCACGCAACTCTGTAAGGAAGACAGTCTCATTCTTCCATAGACCAGGGACATTCTCAAAAACTCACAGTTACTAAGGGGCAAACTGGGAAGCAAACCCTACAGGCCAGGCTCCTGAGCTGTGTTTTCAACTGCTCTGCTCCCTCCAGAATTCTACTTAGAGATTTTCTGCGATGAAAACATCCTGCATTCCTAGGATAAACATAAGTTGCTTACA... |
Task1_train_45733 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | AAGCTAGCGGGGAGGAAACTGATCAAACACCCAGGTGCCGACACCCTTGCCAGCCCCAGAGGGAATCACCCAGCGGGGCGAGGGTGGCTTGTCTTCTCTTTTCCGTCTACTCTCTTTTCTCTTAAAGTTATAAGAATGTATTAAGCGACGTGCTATTTAAACAATGTTGGTTTTGTTGTGACTTTGAAAGACTAAGAGGTTTTAGCTTTGGTTCAATCTCCGTTAATGTCTCAGCCTTGGCTAAGCACTAAGTGATCTATCTCCTGAAATTGTGCCCGTCTGACCTTGGGTGCCCCTGAAAGGCCAGTGTTTATTTGGCT... | AAGCTAGCGGGGAGGAAACTGATCAAACACCCAGGTGCCGACACCCTTGCCAGCCCCAGAGGGAATCACCCAGCGGGGCGAGGGTGGCTTGTCTTCTCTTTTCCGTCTACTCTCTTTTCTCTTAAAGTTATAAGAATGTATTAAGCGACGTGCTATTTAAACAATGTTGGTTTTGTTGTGACTTTGAAAGACTAAGAGGTTTTAGCTTTGGTTCAATCTCCGTTAATGTCTCAGCCTTGGCTAAGCACTAAGTGATCTATCTCCTGAAATTGTGCCCGTCTGACCTTGGGTGCCCCTGAAAGGCCAGTGTTTATTTGGCT... |
Task1_train_45734 | With a mutation on Chromosome 17, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | AGTTCAAGACCAGCCTAGCCAACATGGTGAAACCCTGTGTCTATTAAAAATACAAAAAATTAGCCAGGCATGGTGGCAGGCGCCTATAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTAAGCCCAGGAGACAGAGGTACTGAGTCGAGACTGCACCACTGCACTCTAGCCTGGGCAACAGAGCAAGACTCCGTCTCAATCAATCAATCAATCAATAAAGGCAAGATTAGGGAAAGAGTCCCTGTGAGGGAATGTGCCCTGGAGGACGGTATAATGACAGATTGCTTTTTTTTTTTTTTTTTGAGACGAGTC... | AGTTCAAGACCAGCCTAGCCAACATGGTGAAACCCTGTGTCTATTAAAAATACAAAAAATTAGCCAGGCATGGTGGCAGGCGCCTATAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTAAGCCCAGGAGACAGAGGTACTGAGTCGAGACTGCACCACTGCACTCTAGCCTGGGCAACAGAGCAAGACTCCGTCTCAATCAATCAATCAATCAATAAAGGCAAGATTAGGGAAAGAGTCCCTGTGAGGGAATGTGCCCTGGAGGACGGTATAATGACAGATTGCTTTTTTTTTTTTTTTTTGAGACGAGTC... |
Task1_train_45735 | This sequence change occurs on Chromosome 17. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GATCACACTGCTGCACTCCAGCCTGGGTGACAGAGCAAGACTCCATCTCAAAAAAAAAAAAAAAAAGCCCGCTACAGACATCCCCCGCAGAGGCTCCAAAGCCCCCGAGCGACGGTGTGTGTGGAAGAAATTCCCGGCTTCCCAAGATGAGTAAGACGTCGCGGTCATCTTGGTGTGTAATATGGGCAGAGAAAGAAATCTGTCAGGATTTTAACTTTCCTTAGACATAAGAGGAGTTAGAGGAGAAAGAGTCTGGCCCAGGGCCTTTGGAGATGAGCCCTTGCTTTCACTGTTTGCCTCTCAAGAAAGAGCTGGAGTCC... | GATCACACTGCTGCACTCCAGCCTGGGTGACAGAGCAAGACTCCATCTCAAAAAAAAAAAAAAAAAGCCCGCTACAGACATCCCCCGCAGAGGCTCCAAAGCCCCCGAGCGACGGTGTGTGTGGAAGAAATTCCCGGCTTCCCAAGATGAGTAAGACGTCGCGGTCATCTTGGTGTGTAATATGGGCAGAGAAAGAAATCTGTCAGGATTTTAACTTTCCTTAGACATAAGAGGAGTTAGAGGAGAAAGAGTCTGGCCCAGGGCCTTTGGAGATGAGCCCTTGCTTTCACTGTTTGCCTCTCAAGAAAGAGCTGGAGTCC... |
Task1_train_45736 | This sequence variant lies on Chromosome 17. Is it clinically significant, and what condition might it cause if any? | Benign | CCGAGGCTGTAGTTCAGATTCACAGGTAGGGATGCCAGATTTAGCAAATGCATAGACAGCATCCTAGTTCAGTTTGAATTTTAGATAAATATGCAATAACTTTTTAATATAAGCTTGTCCTATGTCCCAGGCATCATTTATTTGGAATTCAAATTTAACTGATTGCTCTGTATGTTATCTGAAAACACCAGAAGGTTAGGGTTTTAGAGGGCCCACTCAGGCCTCAAACGGATCCAGAGCCCCAGTATGAGCCAATGTGAGCTCAAGGCAGACAGGGCCCCTCCAGGCTTGGCCTGACATCCAGAGAGACCACGAGCCAC... | CCGAGGCTGTAGTTCAGATTCACAGGTAGGGATGCCAGATTTAGCAAATGCATAGACAGCATCCTAGTTCAGTTTGAATTTTAGATAAATATGCAATAACTTTTTAATATAAGCTTGTCCTATGTCCCAGGCATCATTTATTTGGAATTCAAATTTAACTGATTGCTCTGTATGTTATCTGAAAACACCAGAAGGTTAGGGTTTTAGAGGGCCCACTCAGGCCTCAAACGGATCCAGAGCCCCAGTATGAGCCAATGTGAGCTCAAGGCAGACAGGGCCCCTCCAGGCTTGGCCTGACATCCAGAGAGACCACGAGCCAC... |
Task1_train_45737 | Here is a mutation located on Chromosome 17. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CGGCCCAAGGGCCACGGTTTGCCGATTCCTGGGTCAGAACAATGCTTCTCAGCTTTAGCCTCAATCCCGATCGTTGATGGGCTTCCGTCACCAGGACTGCTGGTCTGCACTGGCAGAGTGTCTGATTCACGGGATATATGGGGATTTGAATGTCTACCAAGTGGTCAGGTGATACTGAAGCTGCTGGTTCGAGAACCTCGCTTTGAAAACTGTGGGTGGAGGGAAAGTGATTCCCGTGGCTGACCTTGTTTCTCTCCTATCCTCACAGGGACTTTCATCACGGAGTGGAATGAAGGGGGAAGGCTCTGTGAAGCCTTCCT... | CGGCCCAAGGGCCACGGTTTGCCGATTCCTGGGTCAGAACAATGCTTCTCAGCTTTAGCCTCAATCCCGATCGTTGATGGGCTTCCGTCACCAGGACTGCTGGTCTGCACTGGCAGAGTGTCTGATTCACGGGATATATGGGGATTTGAATGTCTACCAAGTGGTCAGGTGATACTGAAGCTGCTGGTTCGAGAACCTCGCTTTGAAAACTGTGGGTGGAGGGAAAGTGATTCCCGTGGCTGACCTTGTTTCTCTCCTATCCTCACAGGGACTTTCATCACGGAGTGGAATGAAGGGGGAAGGCTCTGTGAAGCCTTCCT... |
Task1_train_45738 | This mutation on Chromosome 17 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TTCTGTGTTCATGTCCTTCTTGCCGCAATAAGAAAGGACGGTCGTCTGTTTGGCTGGACTCCACTTGCGGGGCTGTGGCGGGGAGGGCCTTTCAGAACTGCAGCTTCGCCTGTGGGTCTGTTTGCTCTGCATCCCCCTGTCTGTCCAGCGCTGGATACTTCTCATGATAGATAGATCTGGGGCTCACTGAGGCTCTCACCTTGTTCTTCTCTTTCAGCTGGCCGCTGTGGGGAACATGCCTCCTTTCCTGCGGTACCTCACCACACAGCTGCACCGGCAGGTCCCAGGGGGCCTGGTGCTCTGGTATGACAGCGTGGTGC... | TTCTGTGTTCATGTCCTTCTTGCCGCAATAAGAAAGGACGGTCGTCTGTTTGGCTGGACTCCACTTGCGGGGCTGTGGCGGGGAGGGCCTTTCAGAACTGCAGCTTCGCCTGTGGGTCTGTTTGCTCTGCATCCCCCTGTCTGTCCAGCGCTGGATACTTCTCATGATAGATAGATCTGGGGCTCACTGAGGCTCTCACCTTGTTCTTCTCTTTCAGCTGGCCGCTGTGGGGAACATGCCTCCTTTCCTGCGGTACCTCACCACACAGCTGCACCGGCAGGTCCCAGGGGGCCTGGTGCTCTGGTATGACAGCGTGGTGC... |
Task1_train_45739 | A variant was discovered on Chromosome 17. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | AAGGACGGTCGTCTGTTTGGCTGGACTCCACTTGCGGGGCTGTGGCGGGGAGGGCCTTTCAGAACTGCAGCTTCGCCTGTGGGTCTGTTTGCTCTGCATCCCCCTGTCTGTCCAGCGCTGGATACTTCTCATGATAGATAGATCTGGGGCTCACTGAGGCTCTCACCTTGTTCTTCTCTTTCAGCTGGCCGCTGTGGGGAACATGCCTCCTTTCCTGCGGTACCTCACCACACAGCTGCACCGGCAGGTCCCAGGGGGCCTGGTGCTCTGGTATGACAGCGTGGTGCAAAGTGGGCAGCTCAAATGGCAAGACGAACTCA... | AAGGACGGTCGTCTGTTTGGCTGGACTCCACTTGCGGGGCTGTGGCGGGGAGGGCCTTTCAGAACTGCAGCTTCGCCTGTGGGTCTGTTTGCTCTGCATCCCCCTGTCTGTCCAGCGCTGGATACTTCTCATGATAGATAGATCTGGGGCTCACTGAGGCTCTCACCTTGTTCTTCTCTTTCAGCTGGCCGCTGTGGGGAACATGCCTCCTTTCCTGCGGTACCTCACCACACAGCTGCACCGGCAGGTCCCAGGGGGCCTGGTGCTCTGGTATGACAGCGTGGTGCAAAGTGGGCAGCTCAAATGGCAAGACGAACTCA... |
Task1_train_45740 | Located on Chromosome 17, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | CTGTTTGCTCTGCATCCCCCTGTCTGTCCAGCGCTGGATACTTCTCATGATAGATAGATCTGGGGCTCACTGAGGCTCTCACCTTGTTCTTCTCTTTCAGCTGGCCGCTGTGGGGAACATGCCTCCTTTCCTGCGGTACCTCACCACACAGCTGCACCGGCAGGTCCCAGGGGGCCTGGTGCTCTGGTATGACAGCGTGGTGCAAAGTGGGCAGCTCAAATGGCAAGACGAACTCAACCAGCACAACAGGTGAGCCTGCAGACAGGTGCTGTGAGGGGGCAGGTGCCGTGGTGGGGGCGGGTACTGTGAGGGGTGGGTGC... | CTGTTTGCTCTGCATCCCCCTGTCTGTCCAGCGCTGGATACTTCTCATGATAGATAGATCTGGGGCTCACTGAGGCTCTCACCTTGTTCTTCTCTTTCAGCTGGCCGCTGTGGGGAACATGCCTCCTTTCCTGCGGTACCTCACCACACAGCTGCACCGGCAGGTCCCAGGGGGCCTGGTGCTCTGGTATGACAGCGTGGTGCAAAGTGGGCAGCTCAAATGGCAAGACGAACTCAACCAGCACAACAGGTGAGCCTGCAGACAGGTGCTGTGAGGGGGCAGGTGCCGTGGTGGGGGCGGGTACTGTGAGGGGTGGGTGC... |
Task1_train_45741 | A variant affecting Chromosome 17 has been observed. Determine if it's benign or associated with disease. | Benign | ACTTGCCAGCAGGCACGGTGGTGGTCTTACCCTTCCCTGCCGCTCCGGGCACCCCTGCTCTGTTGGCCTCTGCTGAGTGCCCCTGTTCTGCCCTTTTCTTCAGGAAGAGGCGGTAGGGCCCTGGTACCACCTGAGCGCCCAGGAGATCCAGCCCTTGTTTGGAGAACACAGGCTGGGAGGGGATGGCCGGGGCTGGGTGAGGACGCACTGCTGCCTGGAGGATGCCTGGCACGGAGGCAGCTCCCTGCTCGTCCGGGGTGTGATCCCACCGGAGGTTGGAAATGTGGCTGTGAGGTGGGTGAGTGACGGAGGACGGTGGG... | ACTTGCCAGCAGGCACGGTGGTGGTCTTACCCTTCCCTGCCGCTCCGGGCACCCCTGCTCTGTTGGCCTCTGCTGAGTGCCCCTGTTCTGCCCTTTTCTTCAGGAAGAGGCGGTAGGGCCCTGGTACCACCTGAGCGCCCAGGAGATCCAGCCCTTGTTTGGAGAACACAGGCTGGGAGGGGATGGCCGGGGCTGGGTGAGGACGCACTGCTGCCTGGAGGATGCCTGGCACGGAGGCAGCTCCCTGCTCGTCCGGGGTGTGATCCCACCGGAGGTTGGAAATGTGGCTGTGAGGTGGGTGAGTGACGGAGGACGGTGGG... |
Task1_train_45742 | Chromosome 17 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CTGCAGAAACCCAGAGCTACGCTTCCTGCTGCCTGGGACATTCCTGCCATGCCTGGGTGGCTGTACAGCAGATCTGTCCCCAATAACCTGACCTGGCCACCCCAGAGATTCCCAAGTCAGTCCTATGCTCATGGAAAACCGGGAGGGGCTGGGAACCTGACCTCGGAGGCCTATCCTGACTCCCTGTGATTCAGTGTCAACTGGGAATTTAGGGCAATGGCCATGGCCTGGGATTGGATGACTTCCTGCCTGTCAGTTTGGGGGCTCCCCAGTGGCTCCTGGGCTGTGTCCAGGAGTCCCCAGATGTCACAGGTGGTCCT... | CTGCAGAAACCCAGAGCTACGCTTCCTGCTGCCTGGGACATTCCTGCCATGCCTGGGTGGCTGTACAGCAGATCTGTCCCCAATAACCTGACCTGGCCACCCCAGAGATTCCCAAGTCAGTCCTATGCTCATGGAAAACCGGGAGGGGCTGGGAACCTGACCTCGGAGGCCTATCCTGACTCCCTGTGATTCAGTGTCAACTGGGAATTTAGGGCAATGGCCATGGCCTGGGATTGGATGACTTCCTGCCTGTCAGTTTGGGGGCTCCCCAGTGGCTCCTGGGCTGTGTCCAGGAGTCCCCAGATGTCACAGGTGGTCCT... |
Task1_train_45743 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | CAGATTCCGCCACGGCCTACAGGCTCCTCCTGGTCGACCCTCTCGGGAGCCCCGGTGCCTCCCTTCCTCCATGCCTGGTCCCTCTGCCTGAAGCCTTCCCGCCCTCTCTCCTGGCTCCATGCATCCTGTGGGCCTCCCACAACGCTGGTGCCAGCAAAGCCCGATCTCCTCTCCCGAGGCCGCCTGCATTCCCCCTGTGCGTGCATCGTAACCTGTGTCCCTGACTCACAGGGATCCTTACCCTCCCCAAGGTCTGTGCTCCCCAGGGAGGAGCCAAACCTCTGGGTGCCCTGAGCCCCAGCCCTGCAGAGCAGGCACCC... | CAGATTCCGCCACGGCCTACAGGCTCCTCCTGGTCGACCCTCTCGGGAGCCCCGGTGCCTCCCTTCCTCCATGCCTGGTCCCTCTGCCTGAAGCCTTCCCGCCCTCTCTCCTGGCTCCATGCATCCTGTGGGCCTCCCACAACGCTGGTGCCAGCAAAGCCCGATCTCCTCTCCCGAGGCCGCCTGCATTCCCCCTGTGCGTGCATCGTAACCTGTGTCCCTGACTCACAGGGATCCTTACCCTCCCCAAGGTCTGTGCTCCCCAGGGAGGAGCCAAACCTCTGGGTGCCCTGAGCCCCAGCCCTGCAGAGCAGGCACCC... |
Task1_train_45744 | A genomic change on Chromosome 17 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TGTCCCTGACTCACAGGGATCCTTACCCTCCCCAAGGTCTGTGCTCCCCAGGGAGGAGCCAAACCTCTGGGTGCCCTGAGCCCCAGCCCTGCAGAGCAGGCACCCCACGCGGTGGTTGCAGGCACCGGGCAGTCGCTCCATCCTGGTTTTCAGCTTTTGGTGCACAGAAGCATGAAGAAGAGGGGTCACTGGCACGGAGTCCTCCTTGAGAGTGTGTTCCAGTCGGCCAGGCAGGGGCAGCCGGGGATCCGTACCAGTGGTCCCTGCCCACCTGGGTTAGGAAAGGCTGGCTGGCCTGGGGAGGCTGTGGACGGCGTCTG... | TGTCCCTGACTCACAGGGATCCTTACCCTCCCCAAGGTCTGTGCTCCCCAGGGAGGAGCCAAACCTCTGGGTGCCCTGAGCCCCAGCCCTGCAGAGCAGGCACCCCACGCGGTGGTTGCAGGCACCGGGCAGTCGCTCCATCCTGGTTTTCAGCTTTTGGTGCACAGAAGCATGAAGAAGAGGGGTCACTGGCACGGAGTCCTCCTTGAGAGTGTGTTCCAGTCGGCCAGGCAGGGGCAGCCGGGGATCCGTACCAGTGGTCCCTGCCCACCTGGGTTAGGAAAGGCTGGCTGGCCTGGGGAGGCTGTGGACGGCGTCTG... |
Task1_train_45745 | This sequence change occurs on Chromosome 17. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TCTGACGGATCCTTTTGCAGTGATTTGAACTGTGGCTGGTGCGAGACACAGCGGAGGGGTTGCAGGAAGGTGGACGCCCAGCTTCTCTGGGAGAGGAATGTGGGGAGGGAGAGGGAGGGCACGATCTCCACAGCCTGCACAGCATAGGCAGATTTCAGTTCCCAGGACAGGCAGGGCGTAGGGCCGTCCAGCCCCACCACATGCTGACAGCGGACGGATAGCATCAAAAGCCTTTCTCGCTCAGGGGTCACTGAACAGTTAAAGGCCTCACCTGGCAGCAACCTTCCCATTCCACAGAGCTCACTCTCAGCTCATCAGCA... | TCTGACGGATCCTTTTGCAGTGATTTGAACTGTGGCTGGTGCGAGACACAGCGGAGGGGTTGCAGGAAGGTGGACGCCCAGCTTCTCTGGGAGAGGAATGTGGGGAGGGAGAGGGAGGGCACGATCTCCACAGCCTGCACAGCATAGGCAGATTTCAGTTCCCAGGACAGGCAGGGCGTAGGGCCGTCCAGCCCCACCACATGCTGACAGCGGACGGATAGCATCAAAAGCCTTTCTCGCTCAGGGGTCACTGAACAGTTAAAGGCCTCACCTGGCAGCAACCTTCCCATTCCACAGAGCTCACTCTCAGCTCATCAGCA... |
Task1_train_45746 | This alteration occurs on Chromosome 17. Is it associated with a disease or is it a benign variant? | Benign | TGACTGCACTTATCCCACCCTATCACTCACGTTCCTGGGAGACCCATTTTTGAAAGAAACTATGGGTCACGAAACATATTATCAATGCTGAATTGCACCTCAAATTGCCTTTTCAAATGACATTTTCCTCCGCGGCTCGGCGGGGTGGGCCGGGCTGGCCCCGGCGGTTACCTTTTCTGCTGGATCTCAGAGTACTCCTTTCGCTTCTGCAGCCGCAGCGCCTCCCGCTCCTCCGACGTGGACTCGTGGCTGTAATAGCGCAGCAGGAAGGGCCAGACCTCCCCGCGGATTGACACATCAATACCGCCAAAGAAAATGGC... | TGACTGCACTTATCCCACCCTATCACTCACGTTCCTGGGAGACCCATTTTTGAAAGAAACTATGGGTCACGAAACATATTATCAATGCTGAATTGCACCTCAAATTGCCTTTTCAAATGACATTTTCCTCCGCGGCTCGGCGGGGTGGGCCGGGCTGGCCCCGGCGGTTACCTTTTCTGCTGGATCTCAGAGTACTCCTTTCGCTTCTGCAGCCGCAGCGCCTCCCGCTCCTCCGACGTGGACTCGTGGCTGTAATAGCGCAGCAGGAAGGGCCAGACCTCCCCGCGGATTGACACATCAATACCGCCAAAGAAAATGGC... |
Task1_train_45747 | A change on Chromosome 17 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CTTTTCCCAGGAATAAAAGCCTCTCTCTCTTCTGAAAGGAGGGCAAGGGCCGTCCCCTGCATACAAACCCCTAAATGGCGAGTGTAATTAGGCGCAATTAAAATGAAAATACCTTCATCTTAAAATCGGTTTCCCTCTGCGGCTCTCTCCTCCCCGGCCCACTGTGCCGCCGCCCCCCACTCTCTCCAACCCCAGCCGCAAAAACGGAATGAATGCCTCGTTCGGCCTAACTTCCCTCTGCCGGGAGGGCCTGCAATGAATTACATGTGATTGGCCACATACAAAGGGATCGCTGTTCTGCGAGCAGGGAGCCAGCCTGT... | CTTTTCCCAGGAATAAAAGCCTCTCTCTCTTCTGAAAGGAGGGCAAGGGCCGTCCCCTGCATACAAACCCCTAAATGGCGAGTGTAATTAGGCGCAATTAAAATGAAAATACCTTCATCTTAAAATCGGTTTCCCTCTGCGGCTCTCTCCTCCCCGGCCCACTGTGCCGCCGCCCCCCACTCTCTCCAACCCCAGCCGCAAAAACGGAATGAATGCCTCGTTCGGCCTAACTTCCCTCTGCCGGGAGGGCCTGCAATGAATTACATGTGATTGGCCACATACAAAGGGATCGCTGTTCTGCGAGCAGGGAGCCAGCCTGT... |
Task1_train_45748 | Here is a genetic alteration on Chromosome 17. Based on the data, is it a benign variant or a cause of disease? | Benign | AAGAGGCGCATCATGCAGCAATGGGCCAGCAGCCTGGTGGGCATGAAGCACCGCGACGAGGCGCACAGGGCGGTGCTGGAGGCGCTCAGGTACTGCAGGGCCACAGGCAGCGAGGATGTGCGGGAACCCCAGGGGTCCGTGGCAGGCCCGCCCCACACCCCCTCTCTCTGGGTCCACCGGATCTCTGGGACAGAGGGTGCACCTTGATCCCCGGGTCCGGGCTTCCGTCCGGAAAGCTCCCTCATTGTTTGGTAAGATTTCAGCGATTCTTAAATCCTTTCCAACACTGCGGCGCTGGGAGGGGAGAGGCTTTTCTGCTC... | AAGAGGCGCATCATGCAGCAATGGGCCAGCAGCCTGGTGGGCATGAAGCACCGCGACGAGGCGCACAGGGCGGTGCTGGAGGCGCTCAGGTACTGCAGGGCCACAGGCAGCGAGGATGTGCGGGAACCCCAGGGGTCCGTGGCAGGCCCGCCCCACACCCCCTCTCTCTGGGTCCACCGGATCTCTGGGACAGAGGGTGCACCTTGATCCCCGGGTCCGGGCTTCCGTCCGGAAAGCTCCCTCATTGTTTGGTAAGATTTCAGCGATTCTTAAATCCTTTCCAACACTGCGGCGCTGGGAGGGGAGAGGCTTTTCTGCTC... |
Task1_train_45749 | A mutation found on Chromosome 17 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | ACAGGCAGCGAGGATGTGCGGGAACCCCAGGGGTCCGTGGCAGGCCCGCCCCACACCCCCTCTCTCTGGGTCCACCGGATCTCTGGGACAGAGGGTGCACCTTGATCCCCGGGTCCGGGCTTCCGTCCGGAAAGCTCCCTCATTGTTTGGTAAGATTTCAGCGATTCTTAAATCCTTTCCAACACTGCGGCGCTGGGAGGGGAGAGGCTTTTCTGCTCAGATTTCCTGGCAGGATTAAGTAGAAACAGAGCAGGGTAAAGAGAAAGCTATCTTTGGGAGGTAAAGGTGTCCCTTTGATTTGCAGTATCACCACCTGAGTG... | ACAGGCAGCGAGGATGTGCGGGAACCCCAGGGGTCCGTGGCAGGCCCGCCCCACACCCCCTCTCTCTGGGTCCACCGGATCTCTGGGACAGAGGGTGCACCTTGATCCCCGGGTCCGGGCTTCCGTCCGGAAAGCTCCCTCATTGTTTGGTAAGATTTCAGCGATTCTTAAATCCTTTCCAACACTGCGGCGCTGGGAGGGGAGAGGCTTTTCTGCTCAGATTTCCTGGCAGGATTAAGTAGAAACAGAGCAGGGTAAAGAGAAAGCTATCTTTGGGAGGTAAAGGTGTCCCTTTGATTTGCAGTATCACCACCTGAGTG... |
Task1_train_45750 | Given this variant on Chromosome 17, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GCAGCGAGGATGTGCGGGAACCCCAGGGGTCCGTGGCAGGCCCGCCCCACACCCCCTCTCTCTGGGTCCACCGGATCTCTGGGACAGAGGGTGCACCTTGATCCCCGGGTCCGGGCTTCCGTCCGGAAAGCTCCCTCATTGTTTGGTAAGATTTCAGCGATTCTTAAATCCTTTCCAACACTGCGGCGCTGGGAGGGGAGAGGCTTTTCTGCTCAGATTTCCTGGCAGGATTAAGTAGAAACAGAGCAGGGTAAAGAGAAAGCTATCTTTGGGAGGTAAAGGTGTCCCTTTGATTTGCAGTATCACCACCTGAGTGCGGA... | GCAGCGAGGATGTGCGGGAACCCCAGGGGTCCGTGGCAGGCCCGCCCCACACCCCCTCTCTCTGGGTCCACCGGATCTCTGGGACAGAGGGTGCACCTTGATCCCCGGGTCCGGGCTTCCGTCCGGAAAGCTCCCTCATTGTTTGGTAAGATTTCAGCGATTCTTAAATCCTTTCCAACACTGCGGCGCTGGGAGGGGAGAGGCTTTTCTGCTCAGATTTCCTGGCAGGATTAAGTAGAAACAGAGCAGGGTAAAGAGAAAGCTATCTTTGGGAGGTAAAGGTGTCCCTTTGATTTGCAGTATCACCACCTGAGTGCGGA... |
Task1_train_45751 | This variant lies on Chromosome 17. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GCGAGACTCTGTCTCAAAAAAAAAAATACTGGATGGCCAGGCGCAGTGGCCCACACCTGTAATTCCAACACTTTGGGAGGCCGAGGCAGGTGGATCACTTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACAAAAATACAAAAATTAGCTGGGCATGGTGGCACACACCTGTAATCCCAGCTACTTGAGTGGCTTGAGGCTGCAGTGAGCTGAGATCATGCCATTGCACTCTAGCCTGGGTAACAGAGTGAGAGACTGTCTCAAAAAAAAAAAAAGAAAGAAAGGAATGAAAGGAATG... | GCGAGACTCTGTCTCAAAAAAAAAAATACTGGATGGCCAGGCGCAGTGGCCCACACCTGTAATTCCAACACTTTGGGAGGCCGAGGCAGGTGGATCACTTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACAAAAATACAAAAATTAGCTGGGCATGGTGGCACACACCTGTAATCCCAGCTACTTGAGTGGCTTGAGGCTGCAGTGAGCTGAGATCATGCCATTGCACTCTAGCCTGGGTAACAGAGTGAGAGACTGTCTCAAAAAAAAAAAAAGAAAGAAAGGAATGAAAGGAATG... |
Task1_train_45752 | Here is a variant on Chromosome 17. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GCTAACTTGTGTCAGAATTGCAGGCAATTGAATGTGTTCTCTGTCCTGGCCTGTATTTTCACATTTCCTCACAATGTGTGTGCTACGATTTAAGAAGTGTGTTAGTCTGATCTCACACTGCTGTAGGAAATACCTAAGACTGGATAACTGATAAAGGAAAGAGGTTTAATTGACTGACAGTTCTGCATGGCTGGGGAGGCCTCAGGAAACTTACAATCATGGCAAAAGGCGAAACAGGCACCTCCTTCACAAGGCAGCAGGAGAGAGAGTGTGTGTGAAGCAGGAACCGTCAAACACACAAAACCATCAGATCTCATGAG... | GCTAACTTGTGTCAGAATTGCAGGCAATTGAATGTGTTCTCTGTCCTGGCCTGTATTTTCACATTTCCTCACAATGTGTGTGCTACGATTTAAGAAGTGTGTTAGTCTGATCTCACACTGCTGTAGGAAATACCTAAGACTGGATAACTGATAAAGGAAAGAGGTTTAATTGACTGACAGTTCTGCATGGCTGGGGAGGCCTCAGGAAACTTACAATCATGGCAAAAGGCGAAACAGGCACCTCCTTCACAAGGCAGCAGGAGAGAGAGTGTGTGTGAAGCAGGAACCGTCAAACACACAAAACCATCAGATCTCATGAG... |
Task1_train_45753 | The following genetic variant occurs on Chromosome 17. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GATCTGCAAAGTCGCCAGAGGTTAAGTCCTTTCTCTCTTGTGGCTTTGCCACCCCTGGAGTGTCACCCTCAGCTGCGGTGCCCAGGATTCCCCACTGTGGTATGTCCGTGCACCAGTCAATAGGAAAGGGAGCAAGGAAAGGTACTGGGTCCCCCTAAGGACATACGAGTTGCCAGAATCACTTCCGCTGACACCCAGTGGACCAAGCCGCACCTTTATGCAGAAGTGGGGCTCCCAGCCAGGCGTGGTCACTCCTGAAATCCCAGCACTTCGGAAGGCCAAGGGGGGTGGATCACTTGAGCTCAGGAGTTCGAGACCAG... | GATCTGCAAAGTCGCCAGAGGTTAAGTCCTTTCTCTCTTGTGGCTTTGCCACCCCTGGAGTGTCACCCTCAGCTGCGGTGCCCAGGATTCCCCACTGTGGTATGTCCGTGCACCAGTCAATAGGAAAGGGAGCAAGGAAAGGTACTGGGTCCCCCTAAGGACATACGAGTTGCCAGAATCACTTCCGCTGACACCCAGTGGACCAAGCCGCACCTTTATGCAGAAGTGGGGCTCCCAGCCAGGCGTGGTCACTCCTGAAATCCCAGCACTTCGGAAGGCCAAGGGGGGTGGATCACTTGAGCTCAGGAGTTCGAGACCAG... |
Task1_train_45754 | Mutation context: Chromosome 17. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CTGCGGTGCCCAGGATTCCCCACTGTGGTATGTCCGTGCACCAGTCAATAGGAAAGGGAGCAAGGAAAGGTACTGGGTCCCCCTAAGGACATACGAGTTGCCAGAATCACTTCCGCTGACACCCAGTGGACCAAGCCGCACCTTTATGCAGAAGTGGGGCTCCCAGCCAGGCGTGGTCACTCCTGAAATCCCAGCACTTCGGAAGGCCAAGGGGGGTGGATCACTTGAGCTCAGGAGTTCGAGACCAGCCTGGGTAACATGGCAAAATCCCGTCTCTACAAAAATACAGAAAATTAGCTGGGTGCGGTGGTGTGTGCCTA... | CTGCGGTGCCCAGGATTCCCCACTGTGGTATGTCCGTGCACCAGTCAATAGGAAAGGGAGCAAGGAAAGGTACTGGGTCCCCCTAAGGACATACGAGTTGCCAGAATCACTTCCGCTGACACCCAGTGGACCAAGCCGCACCTTTATGCAGAAGTGGGGCTCCCAGCCAGGCGTGGTCACTCCTGAAATCCCAGCACTTCGGAAGGCCAAGGGGGGTGGATCACTTGAGCTCAGGAGTTCGAGACCAGCCTGGGTAACATGGCAAAATCCCGTCTCTACAAAAATACAGAAAATTAGCTGGGTGCGGTGGTGTGTGCCTA... |
Task1_train_45755 | Mutation context: Chromosome 17. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | AGTCCAATGTCTGGGCTTCTCTAGGGACAATTTTTATTAACTACTGTCCCCCCATCTGTGGGCCATACTTTCTTGTTTCTTTGCGTGTCTCATACATTTTTGTTTCAGACTGGACATTTTAAACGCAGCTGCTGTGGTCATCAGATTCCCCATCCCCCTCAGGTCTCGTTGCTATTGCTGATTGTTTTGTGACTTTCTTGAGCTAATTCCATAAGGTCTGTGTTCTTCATTGTGTGTGGCCACCAAAGTCTCTGCTTGACTAGCTTAGTGGACAGCCAATAATTGGTCAGATATCCTTCACAGATGGCATCCGTGAGTCT... | AGTCCAATGTCTGGGCTTCTCTAGGGACAATTTTTATTAACTACTGTCCCCCCATCTGTGGGCCATACTTTCTTGTTTCTTTGCGTGTCTCATACATTTTTGTTTCAGACTGGACATTTTAAACGCAGCTGCTGTGGTCATCAGATTCCCCATCCCCCTCAGGTCTCGTTGCTATTGCTGATTGTTTTGTGACTTTCTTGAGCTAATTCCATAAGGTCTGTGTTCTTCATTGTGTGTGGCCACCAAAGTCTCTGCTTGACTAGCTTAGTGGACAGCCAATAATTGGTCAGATATCCTTCACAGATGGCATCCGTGAGTCT... |
Task1_train_45756 | Given this context: Chromosome 17 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | ACTGGACATTTTAAACGCAGCTGCTGTGGTCATCAGATTCCCCATCCCCCTCAGGTCTCGTTGCTATTGCTGATTGTTTTGTGACTTTCTTGAGCTAATTCCATAAGGTCTGTGTTCTTCATTGTGTGTGGCCACCAAAGTCTCTGCTTGACTAGCTTAGTGGACAGCCAATAATTGGTCAGATATCCTTCACAGATGGCATCCGTGAGTCTCCCAGCCTTTGCTGGGGCGAGGTGGGGAGCACCGTCAACACTTAGCTAGGCCAAGGATTCTTGCTGTTCTTACAAAGATTCAGCCATTTTGTTAAATACATGCTCCCC... | ACTGGACATTTTAAACGCAGCTGCTGTGGTCATCAGATTCCCCATCCCCCTCAGGTCTCGTTGCTATTGCTGATTGTTTTGTGACTTTCTTGAGCTAATTCCATAAGGTCTGTGTTCTTCATTGTGTGTGGCCACCAAAGTCTCTGCTTGACTAGCTTAGTGGACAGCCAATAATTGGTCAGATATCCTTCACAGATGGCATCCGTGAGTCTCCCAGCCTTTGCTGGGGCGAGGTGGGGAGCACCGTCAACACTTAGCTAGGCCAAGGATTCTTGCTGTTCTTACAAAGATTCAGCCATTTTGTTAAATACATGCTCCCC... |
Task1_train_45757 | A variant on Chromosome 17 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TGTAGCTCATTTCTGTTTGTGATTGGACCGGCCCTCTCTGCTTCCCAAGTCCATGGGCCCGTCATGGGTGGGTGCCTTAATCCTTTCCACCTCGGCGCGACCGGCTCCCAGCCTTGGGCCTTGCACACAGTAGGTGCTTTGCTCCCCATTTGGAATTCACCCCATGGCCACCAGGGGGCGCAAGTGCCCTGCGCTGCCCCTGTGCCTTCTGTGGGTCGCAGAATCAGAAATCTTCATCTTTGGGGACTCATACACGTTTTTATTTATAATCGTGATAAATCGAGAGAGACCACCCAAGGCATATCTAAATTAGATGTGAG... | TGTAGCTCATTTCTGTTTGTGATTGGACCGGCCCTCTCTGCTTCCCAAGTCCATGGGCCCGTCATGGGTGGGTGCCTTAATCCTTTCCACCTCGGCGCGACCGGCTCCCAGCCTTGGGCCTTGCACACAGTAGGTGCTTTGCTCCCCATTTGGAATTCACCCCATGGCCACCAGGGGGCGCAAGTGCCCTGCGCTGCCCCTGTGCCTTCTGTGGGTCGCAGAATCAGAAATCTTCATCTTTGGGGACTCATACACGTTTTTATTTATAATCGTGATAAATCGAGAGAGACCACCCAAGGCATATCTAAATTAGATGTGAG... |
Task1_train_45758 | Given this context: Chromosome 17 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TTTTCCTCTGTGAGGATTCTGCGTAATGCCCTGGTTGCATATACTTTTAGTGGAATTGACCTCAAATACATCCAGAGTACACAGCTCATTTCATTGGCTTTGAATGTGATCCCAATGGGTTTTTGCCTGTGAGCCAGGCCTAGGGAACTCTCAGGTCTCTGCTGGCCCTGGCTCTGCTGTGTGGTTCACAGAGTGAGACTTGCAGCCGTCGACCCTGGCAGGCTGCTCCCTGGTTCGGGGGCTCACAGGCTGTACAGTAAAATGCTAGAGCTTGGGAGACCCTGGGGAGCCTCTAGTCCTAGGATTGACAACTCAGAGAC... | TTTTCCTCTGTGAGGATTCTGCGTAATGCCCTGGTTGCATATACTTTTAGTGGAATTGACCTCAAATACATCCAGAGTACACAGCTCATTTCATTGGCTTTGAATGTGATCCCAATGGGTTTTTGCCTGTGAGCCAGGCCTAGGGAACTCTCAGGTCTCTGCTGGCCCTGGCTCTGCTGTGTGGTTCACAGAGTGAGACTTGCAGCCGTCGACCCTGGCAGGCTGCTCCCTGGTTCGGGGGCTCACAGGCTGTACAGTAAAATGCTAGAGCTTGGGAGACCCTGGGGAGCCTCTAGTCCTAGGATTGACAACTCAGAGAC... |
Task1_train_45759 | A genomic change on Chromosome 17 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CTAGGCCGAGCATGGTGGCTCACACCTGTAATCCAAACACTTTGGGAGGCCGAGGCGGGTGGATCATCTGAGGTCAGGAGTTCGAGACCAGCCTGGGTAACCTGGTGAAACCCTGTCTCTATTAAAAATACAAAAAACTTAGCTGGGCGTGGTGGCAGGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCCGGAGGCAGAGGTTGCAGTGAGCCGGGATTGAGCCATTGCACTCCAGCCTGGGCGACAGAGTGAGACTCTGTCTCAAAAAAAAAAAAAAAGAAAAGGAAACCATTGTT... | CTAGGCCGAGCATGGTGGCTCACACCTGTAATCCAAACACTTTGGGAGGCCGAGGCGGGTGGATCATCTGAGGTCAGGAGTTCGAGACCAGCCTGGGTAACCTGGTGAAACCCTGTCTCTATTAAAAATACAAAAAACTTAGCTGGGCGTGGTGGCAGGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCCGGAGGCAGAGGTTGCAGTGAGCCGGGATTGAGCCATTGCACTCCAGCCTGGGCGACAGAGTGAGACTCTGTCTCAAAAAAAAAAAAAAAGAAAAGGAAACCATTGTT... |
Task1_train_45760 | Here is a mutation located on Chromosome 17. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TCATCTGAGGTCAGGAGTTCGAGACCAGCCTGGGTAACCTGGTGAAACCCTGTCTCTATTAAAAATACAAAAAACTTAGCTGGGCGTGGTGGCAGGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCCGGAGGCAGAGGTTGCAGTGAGCCGGGATTGAGCCATTGCACTCCAGCCTGGGCGACAGAGTGAGACTCTGTCTCAAAAAAAAAAAAAAAGAAAAGGAAACCATTGTTCTAGATCAGCCTATGGGAGGCTCCAAGTTTCAAGTGCACGGAACGCACAGTGCTAGAAAGCAG... | TCATCTGAGGTCAGGAGTTCGAGACCAGCCTGGGTAACCTGGTGAAACCCTGTCTCTATTAAAAATACAAAAAACTTAGCTGGGCGTGGTGGCAGGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCCGGAGGCAGAGGTTGCAGTGAGCCGGGATTGAGCCATTGCACTCCAGCCTGGGCGACAGAGTGAGACTCTGTCTCAAAAAAAAAAAAAAAGAAAAGGAAACCATTGTTCTAGATCAGCCTATGGGAGGCTCCAAGTTTCAAGTGCACGGAACGCACAGTGCTAGAAAGCAG... |
Task1_train_45761 | A mutation found on Chromosome 17 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CTGTGGAAACATCTTCACCCTTTACCAGGCTTGGCATGGTCTGAACTGGAAACCCTGAGAATGTTTCTGCAGTGGGACAGGAGGGACGTCTTCCCATGCCTTCCCTAGAACCGGAGGCCCCGGACTTCTCTGGAAAACCGCCTGTCTGCAGGCCCGATTCAAATCTATGGGGGCTGCACTTCCCTTTTACATTTTGATGTGTCAAAGGCTTTTGGAGTGACCAAAAGCACAGAGGCAGCGGGTGGGGCGCCTGGGTGGTCCCCAAGGTCGCTGCCACCCTTGCCCGGGGCAGAGGCAGAAGCCCACATATGCTGTGACGC... | CTGTGGAAACATCTTCACCCTTTACCAGGCTTGGCATGGTCTGAACTGGAAACCCTGAGAATGTTTCTGCAGTGGGACAGGAGGGACGTCTTCCCATGCCTTCCCTAGAACCGGAGGCCCCGGACTTCTCTGGAAAACCGCCTGTCTGCAGGCCCGATTCAAATCTATGGGGGCTGCACTTCCCTTTTACATTTTGATGTGTCAAAGGCTTTTGGAGTGACCAAAAGCACAGAGGCAGCGGGTGGGGCGCCTGGGTGGTCCCCAAGGTCGCTGCCACCCTTGCCCGGGGCAGAGGCAGAAGCCCACATATGCTGTGACGC... |
Task1_train_45762 | A genetic alteration is present on Chromosome 17. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | ATTTTTTGAGACAGGGTCTCACTGTGTCACCCAGGCTAGAGTACAGTGGCATGATCATGGTTCACTATAGCCTCAACCTCCCAGGCTCAAGTTATCATCTCACCTCAGCCCCCCAAGTAGCTGGGACTATAGGCATATGCCACCATGCTCAACTAATTTTTTATTTTTTGTGGAGACAGTGTCTCACTAATTTGCTCAGGCTGGCCTCAAACTTCTGGGCTCAAGCAGTCCTCCTGTCTTGGCTTCCCAAAGTGTTGGGATTACAGGCATGGGCCACTGCACCCAGCCATATTTTCCTGCTTCTTTGCATGCCTAGTAAT... | ATTTTTTGAGACAGGGTCTCACTGTGTCACCCAGGCTAGAGTACAGTGGCATGATCATGGTTCACTATAGCCTCAACCTCCCAGGCTCAAGTTATCATCTCACCTCAGCCCCCCAAGTAGCTGGGACTATAGGCATATGCCACCATGCTCAACTAATTTTTTATTTTTTGTGGAGACAGTGTCTCACTAATTTGCTCAGGCTGGCCTCAAACTTCTGGGCTCAAGCAGTCCTCCTGTCTTGGCTTCCCAAAGTGTTGGGATTACAGGCATGGGCCACTGCACCCAGCCATATTTTCCTGCTTCTTTGCATGCCTAGTAAT... |
Task1_train_45763 | This sequence variant lies on Chromosome 17. Is it clinically significant, and what condition might it cause if any? | Benign | CCACTTTTGTTTCTTAATTTCATTCTTTCCAGGAAATTGCAGATTTAACAGATGTTAGGTACTTTGGTCGAGCCAAGCTTGATGTAGTTGAGGAACGGAAGAGAAAGTTGGAGGGAAACACGGGCTAGAGTAGAGTAAATCTAAGAAATAAAGTGAGTGTCTCTCTTTCTGTTTAGAGCAAAAAGAAGAAAAGGAAGAAGAAAAAGAAGGGGAACAAGTCCGCTTCCTCAGAGCTGGCTTCCTTGCCCCTTTCTCCTGCCAGCCCCTGTCACCTGACTTTGCTTTCAAACCCGTGGCCTCAGGACACAGCCCTGCCCCAC... | CCACTTTTGTTTCTTAATTTCATTCTTTCCAGGAAATTGCAGATTTAACAGATGTTAGGTACTTTGGTCGAGCCAAGCTTGATGTAGTTGAGGAACGGAAGAGAAAGTTGGAGGGAAACACGGGCTAGAGTAGAGTAAATCTAAGAAATAAAGTGAGTGTCTCTCTTTCTGTTTAGAGCAAAAAGAAGAAAAGGAAGAAGAAAAAGAAGGGGAACAAGTCCGCTTCCTCAGAGCTGGCTTCCTTGCCCCTTTCTCCTGCCAGCCCCTGTCACCTGACTTTGCTTTCAAACCCGTGGCCTCAGGACACAGCCCTGCCCCAC... |
Task1_train_45764 | A variant on Chromosome 17 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | AATGTTCTCCCCATGCCCCTGCCTGTGCCGTGTCTAGTTCAGGAAACACAGTGTGACTGTCCTGGGCCTGAAATGTTCAGTGGTGAGAAGGCGATGGCCTTTGACTTGGTACCTGCTCAGACCCCACTGAGCTCTGCACTCTCTCTGCGTGTGTTGATTTGAACGTGAGAATGACATTAGGTAGCCTTTCCTGACCAGCATGTCTTATCACGACATCTGCCTCTCAGTTTTACACATTTATTTATTTGTTGTTTTGAGACAGTGTCTTACTCTGTTCCCCCAGTCTGGAGTGCAGTGGAGCAATCAGCTCACTGCAGCTT... | AATGTTCTCCCCATGCCCCTGCCTGTGCCGTGTCTAGTTCAGGAAACACAGTGTGACTGTCCTGGGCCTGAAATGTTCAGTGGTGAGAAGGCGATGGCCTTTGACTTGGTACCTGCTCAGACCCCACTGAGCTCTGCACTCTCTCTGCGTGTGTTGATTTGAACGTGAGAATGACATTAGGTAGCCTTTCCTGACCAGCATGTCTTATCACGACATCTGCCTCTCAGTTTTACACATTTATTTATTTGTTGTTTTGAGACAGTGTCTTACTCTGTTCCCCCAGTCTGGAGTGCAGTGGAGCAATCAGCTCACTGCAGCTT... |
Task1_train_45765 | A variant affecting Chromosome 17 has been observed. Determine if it's benign or associated with disease. | Benign | TAGCGACAGCCAAGAGATCTCAGCAGTGCCTCTCTGTGGGCAGGGATGGGGTGAATCACAGCTCCGTGTTTCTGTTTCTGATCCAGCCCTTATAGTCTGTCCCTAGAAGAGCGCTTCGGAGTCTTACTGAGAGGACAGAGAAGAACAAGGGCCCAGGATCTCACCATCATGGGGGTGCGGGATTTTTCCTGACCCCTTCGTTGGACTTGCGACAGGGATGCTGTGTTTACTTGGCCCGCCGTGCTCAACCCCTTGTGGGAGGGAGCACGTGAGTGAGTGTGGCATCTGGCCAGCTGCTTTGGGAGCTGGCAGGAGCAAGC... | TAGCGACAGCCAAGAGATCTCAGCAGTGCCTCTCTGTGGGCAGGGATGGGGTGAATCACAGCTCCGTGTTTCTGTTTCTGATCCAGCCCTTATAGTCTGTCCCTAGAAGAGCGCTTCGGAGTCTTACTGAGAGGACAGAGAAGAACAAGGGCCCAGGATCTCACCATCATGGGGGTGCGGGATTTTTCCTGACCCCTTCGTTGGACTTGCGACAGGGATGCTGTGTTTACTTGGCCCGCCGTGCTCAACCCCTTGTGGGAGGGAGCACGTGAGTGAGTGTGGCATCTGGCCAGCTGCTTTGGGAGCTGGCAGGAGCAAGC... |
Task1_train_45766 | Given this variant on Chromosome 17, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TTTTCTATCTCTGTTTTTTGCTCTGCTCTTGAGAGATTTATTCAGAACCAAACTTTCTGCTTAGGTTTTCATGTCAGCTTTCGTATATATATTTAATGTAGAGGAATTCTTTTTCTCGGAATGTTCCTTTTTAAATTCTGTCCTGTTCTTGTTCACGTTGCAGCATCTTCCCTTCTGGGTTATTCACCGTTTTGTTTTGGAGGTTTTGCTTTTCCTGGCATCATGTGCTGCTTCCTCCAGGTTCCTTTCACTTGTTGATTTGTTTTGATTTTCCTCCTATGTCTGGACATTCTTGTTTGTCTGTGTTTATTAAGAGAAAG... | TTTTCTATCTCTGTTTTTTGCTCTGCTCTTGAGAGATTTATTCAGAACCAAACTTTCTGCTTAGGTTTTCATGTCAGCTTTCGTATATATATTTAATGTAGAGGAATTCTTTTTCTCGGAATGTTCCTTTTTAAATTCTGTCCTGTTCTTGTTCACGTTGCAGCATCTTCCCTTCTGGGTTATTCACCGTTTTGTTTTGGAGGTTTTGCTTTTCCTGGCATCATGTGCTGCTTCCTCCAGGTTCCTTTCACTTGTTGATTTGTTTTGATTTTCCTCCTATGTCTGGACATTCTTGTTTGTCTGTGTTTATTAAGAGAAAG... |
Task1_train_45767 | Located on Chromosome 17, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TTCCTCCAGGTTCCTTTCACTTGTTGATTTGTTTTGATTTTCCTCCTATGTCTGGACATTCTTGTTTGTCTGTGTTTATTAAGAGAAAGCCCTCACAAGTGGGTTGGCCCTCTGCGGGGTGCTGCCGTGGGGTGCTGTGGCTCGACCTGGAAGTTGGCCTGTCTCCTGAAGTCTTCTGTCTCCTGCCTGGAGGGTGTGGGCCTGGCTGCCAGGTTTCTGGGAGCCAAGAGGGAGAAGCGGGCTGGCGGGCCTTGGCATCCCGTGCGTGGTCCTCCCATGGCCCGTGTTCTCAGTGTGGTTCTCCGCCACCTCCCTCTGTC... | TTCCTCCAGGTTCCTTTCACTTGTTGATTTGTTTTGATTTTCCTCCTATGTCTGGACATTCTTGTTTGTCTGTGTTTATTAAGAGAAAGCCCTCACAAGTGGGTTGGCCCTCTGCGGGGTGCTGCCGTGGGGTGCTGTGGCTCGACCTGGAAGTTGGCCTGTCTCCTGAAGTCTTCTGTCTCCTGCCTGGAGGGTGTGGGCCTGGCTGCCAGGTTTCTGGGAGCCAAGAGGGAGAAGCGGGCTGGCGGGCCTTGGCATCCCGTGCGTGGTCCTCCCATGGCCCGTGTTCTCAGTGTGGTTCTCCGCCACCTCCCTCTGTC... |
Task1_train_45768 | Given a variant located on Chromosome 17, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TCTCCTGCCTGGAGGGTGTGGGCCTGGCTGCCAGGTTTCTGGGAGCCAAGAGGGAGAAGCGGGCTGGCGGGCCTTGGCATCCCGTGCGTGGTCCTCCCATGGCCCGTGTTCTCAGTGTGGTTCTCCGCCACCTCCCTCTGTCTCCTGTGTTTCACACCCCATCCTCCTTCCCCCTGAGATTGGATAATTCATGTCTTCTGTTAGCTTCCTGAGAAAGGGGATGTGTCTAGAAAGGCCCTTTGTTCTGCCATGTATCTGTGGCCTCCAATCCACACGCCCCCCTGCGTTATCCTTTCTAGAAAATGAACCATCTCTTGGCT... | TCTCCTGCCTGGAGGGTGTGGGCCTGGCTGCCAGGTTTCTGGGAGCCAAGAGGGAGAAGCGGGCTGGCGGGCCTTGGCATCCCGTGCGTGGTCCTCCCATGGCCCGTGTTCTCAGTGTGGTTCTCCGCCACCTCCCTCTGTCTCCTGTGTTTCACACCCCATCCTCCTTCCCCCTGAGATTGGATAATTCATGTCTTCTGTTAGCTTCCTGAGAAAGGGGATGTGTCTAGAAAGGCCCTTTGTTCTGCCATGTATCTGTGGCCTCCAATCCACACGCCCCCCTGCGTTATCCTTTCTAGAAAATGAACCATCTCTTGGCT... |
Task1_train_45769 | This sequence change occurs on Chromosome 17. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | AGGTCCCCGTGCTCTTTCACCTGGACGTGACCTCCTCAGTAAGTGCCCTCCAGCGTCAGCCGATGGCCACATCAGTAAAGACGTGGTCCCCATGTCTCTGCGTGACTCCTCCCCGTGTATAGAATTCCTTGTTTCCACACGCACAGTCCTGTGAAGCTTAACAGTGGGAATGTGCTCTGAGAAGTGTGTTGTCAGGCAGTTTCCTCCTTGTGTGAACGTCATGGTGTGCGCTTACACTAACCTAGACGTAGAGCCCACTGCACACACAGGCTTTATGGTACACACTGTCGCTCCTAGGCCGCAAACCTGTGCTGCATATG... | AGGTCCCCGTGCTCTTTCACCTGGACGTGACCTCCTCAGTAAGTGCCCTCCAGCGTCAGCCGATGGCCACATCAGTAAAGACGTGGTCCCCATGTCTCTGCGTGACTCCTCCCCGTGTATAGAATTCCTTGTTTCCACACGCACAGTCCTGTGAAGCTTAACAGTGGGAATGTGCTCTGAGAAGTGTGTTGTCAGGCAGTTTCCTCCTTGTGTGAACGTCATGGTGTGCGCTTACACTAACCTAGACGTAGAGCCCACTGCACACACAGGCTTTATGGTACACACTGTCGCTCCTAGGCCGCAAACCTGTGCTGCATATG... |
Task1_train_45770 | A variant on Chromosome 17 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | AGAGACGGCAACCTAGAGTTACTGACCAGGCCAGATACTCCGCCCTGGGCAAGAGATCTTTGGATGTTTATTTTCAGTGACACGATGCTTCTGAACATTCCTCTTGTGATGAATAATGAAAGGTGAGTGGAAGGCTTTCTTTCCCTGGGGAGAGAAACTATCAGAACACAGCAGGACCCTAATATGCTCTCCCAAGTGCTGGGTGAAACGCAGCCCTCAACTTCAGAGCAACGTTGACATGGGTGCTTTCTGCAGTAACAATAGGAAGTTTGGCCGGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCG... | AGAGACGGCAACCTAGAGTTACTGACCAGGCCAGATACTCCGCCCTGGGCAAGAGATCTTTGGATGTTTATTTTCAGTGACACGATGCTTCTGAACATTCCTCTTGTGATGAATAATGAAAGGTGAGTGGAAGGCTTTCTTTCCCTGGGGAGAGAAACTATCAGAACACAGCAGGACCCTAATATGCTCTCCCAAGTGCTGGGTGAAACGCAGCCCTCAACTTCAGAGCAACGTTGACATGGGTGCTTTCTGCAGTAACAATAGGAAGTTTGGCCGGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCG... |
Task1_train_45771 | This sequence change occurs on Chromosome 17. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CCGCCTTCCTTTATTTTATTCCACTGGAAAAATATCCTAGGCCAGGCGCAGTGGTTCACAACACCTTGGGAGGCCAAGGCCGGCAGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGACCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCTGGGTGTGGTGGTGCATGCCTGTAGTCCCAGCTACTTGGTAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCAGAGATCACGCTACCCACCGCACTCCAGCCTGGGCAACAGAGTAAGACTCCATCTCCAAAAA... | CCGCCTTCCTTTATTTTATTCCACTGGAAAAATATCCTAGGCCAGGCGCAGTGGTTCACAACACCTTGGGAGGCCAAGGCCGGCAGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGACCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCTGGGTGTGGTGGTGCATGCCTGTAGTCCCAGCTACTTGGTAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCAGAGATCACGCTACCCACCGCACTCCAGCCTGGGCAACAGAGTAAGACTCCATCTCCAAAAA... |
Task1_train_45772 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | CTGCCCAAGAAGTTCGTGGACATCTTTCAGCAGACTCCTCTGGGCAGGTTTCTTGCCCAGCTCCATGGAGAGCCGCAGCAGGAACTTCTTCAGTGTTACTTGAAGGATTTCATTCTCTTGACCATGCGTGTGTCAACGGAGGAGGAATTAAAGGTAGATGTTTAGATACTGGCTAAGGGTCAGGTGTAGAGCTTGCATGATGGGGACTGGATGCAGACACGGAGACGTTTCCTCAGCTGCCTGGAGCTGGTGCTGTGAAGTCTGGGAACAGAACATGGTCAGCGAAGGGTGCCGGTGGGTGAAGGGGTCGCCCAGTCTCC... | CTGCCCAAGAAGTTCGTGGACATCTTTCAGCAGACTCCTCTGGGCAGGTTTCTTGCCCAGCTCCATGGAGAGCCGCAGCAGGAACTTCTTCAGTGTTACTTGAAGGATTTCATTCTCTTGACCATGCGTGTGTCAACGGAGGAGGAATTAAAGGTAGATGTTTAGATACTGGCTAAGGGTCAGGTGTAGAGCTTGCATGATGGGGACTGGATGCAGACACGGAGACGTTTCCTCAGCTGCCTGGAGCTGGTGCTGTGAAGTCTGGGAACAGAACATGGTCAGCGAAGGGTGCCGGTGGGTGAAGGGGTCGCCCAGTCTCC... |
Task1_train_45773 | This sequence variant lies on Chromosome 17. Is it clinically significant, and what condition might it cause if any? | Benign | CTGCATTGACTGCCATGCGCCGATTGGAGGCATTGACCACAAACCTCGGGACGGCTTTCATCTGGTCAAGTATGTGGGTCAGGATTCTATTTCCTAAGTACTCAAACTTTGGGGTGTTGGGCTGTTTTTATTCCAGCTGATAAAGTGATACTCAAGATAGTACTAATTACTCCAGTACATGTGGGCCTGTGTCATATTGAATAGCAATGCCAAAGTCCCAGCAGTCACACAGCAGGGAGGCATCTGATCTGTTGTTGGATCCCTGGGCCCTGAAATGCAAAGCAGGCTACCCTTTAACAGCTGTTAATATGAATACAGGT... | CTGCATTGACTGCCATGCGCCGATTGGAGGCATTGACCACAAACCTCGGGACGGCTTTCATCTGGTCAAGTATGTGGGTCAGGATTCTATTTCCTAAGTACTCAAACTTTGGGGTGTTGGGCTGTTTTTATTCCAGCTGATAAAGTGATACTCAAGATAGTACTAATTACTCCAGTACATGTGGGCCTGTGTCATATTGAATAGCAATGCCAAAGTCCCAGCAGTCACACAGCAGGGAGGCATCTGATCTGTTGTTGGATCCCTGGGCCCTGAAATGCAAAGCAGGCTACCCTTTAACAGCTGTTAATATGAATACAGGT... |
Task1_train_45774 | A variant affecting Chromosome 17 has been observed. Determine if it's benign or associated with disease. | Benign | TCTCCTGCCTTAGCCTCCCTAGTAGCTGGGATTACAGGTGCCAACCATCACGCCCAGCTAATTTTTTCTATTTTAGTACAGAGACGGGGTTTCTCCACGTGGCCAGGCTGGTCTCGAGCTCCTGACCTCAAGTGATTCACAAGCTTTGGCCACCACACCCAGCCTAAATTACCTCTTCGTATCTTTTTCTTTTGCGCTTTGTCTCTGTAATGGTTGTGAGAGCTCTTTGCATAGAACAGGGGTTCATCTTCTCTGCCGTGTGCCACAGTGCTCTATTTCAGCCTTTAATTTTATGAAGTCAAATCTGACAGAATTTTCCT... | TCTCCTGCCTTAGCCTCCCTAGTAGCTGGGATTACAGGTGCCAACCATCACGCCCAGCTAATTTTTTCTATTTTAGTACAGAGACGGGGTTTCTCCACGTGGCCAGGCTGGTCTCGAGCTCCTGACCTCAAGTGATTCACAAGCTTTGGCCACCACACCCAGCCTAAATTACCTCTTCGTATCTTTTTCTTTTGCGCTTTGTCTCTGTAATGGTTGTGAGAGCTCTTTGCATAGAACAGGGGTTCATCTTCTCTGCCGTGTGCCACAGTGCTCTATTTCAGCCTTTAATTTTATGAAGTCAAATCTGACAGAATTTTCCT... |
Task1_train_45775 | Here is a genetic alteration on Chromosome 17. Based on the data, is it a benign variant or a cause of disease? | Benign | GCACCAGGTCACTGGCTTATGTTGAGATTGCTGGTCATCCAGACCTGCCCCCTACGCTAATCATACAGTGATTTTTCTTTTCCCAGATTTTTAATTTGAAAATGTACATACATCCCCCCAAATTGGAAAAGGATACGTTGGACACCTGTATTCCTTCTACTTAGGTTCAGCTGTTGCTGCTCTGGAATATTCTCTCTCGCGCACATGCGCTCTTTGTGTGCGTGTGTACCGTACATCCCAGCGACTGTGACAGCTCAGAAGACATCAGCAGGCCTGTCCTGAGAATGACATTCTCCTCCACAGCCACAGTGTCATTATCA... | GCACCAGGTCACTGGCTTATGTTGAGATTGCTGGTCATCCAGACCTGCCCCCTACGCTAATCATACAGTGATTTTTCTTTTCCCAGATTTTTAATTTGAAAATGTACATACATCCCCCCAAATTGGAAAAGGATACGTTGGACACCTGTATTCCTTCTACTTAGGTTCAGCTGTTGCTGCTCTGGAATATTCTCTCTCGCGCACATGCGCTCTTTGTGTGCGTGTGTACCGTACATCCCAGCGACTGTGACAGCTCAGAAGACATCAGCAGGCCTGTCCTGAGAATGACATTCTCCTCCACAGCCACAGTGTCATTATCA... |
Task1_train_45776 | A variant on Chromosome 17 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TCCCTCCCTGCTAGGGTCTGCCCCCATCCCAGCCTGTGGCCCACCGCCCTCTTTTATCTTGGTGATTCTGGAGACGGGACAGGGGTTACTGCTGATCTAGTCAGGGAGAGGACAGACCAGCTGGGCTCAGAGCCCCCAGAGAAGCAAGTGTTAGCAGGGAAGCCTCGGCTTGCGCAGAGCCTACAGGGAAGCACAGACTGGAAACCAGTGAAGGCTGAGCAGCTCCAACTGCCACTGGTGGGGAGGAGACCCAGGACCCCCTCACTCAGCCTGTCCACTCACCAGCTACTCAGGCCCTTCAGGGACTGCCCAGCTCGGTT... | TCCCTCCCTGCTAGGGTCTGCCCCCATCCCAGCCTGTGGCCCACCGCCCTCTTTTATCTTGGTGATTCTGGAGACGGGACAGGGGTTACTGCTGATCTAGTCAGGGAGAGGACAGACCAGCTGGGCTCAGAGCCCCCAGAGAAGCAAGTGTTAGCAGGGAAGCCTCGGCTTGCGCAGAGCCTACAGGGAAGCACAGACTGGAAACCAGTGAAGGCTGAGCAGCTCCAACTGCCACTGGTGGGGAGGAGACCCAGGACCCCCTCACTCAGCCTGTCCACTCACCAGCTACTCAGGCCCTTCAGGGACTGCCCAGCTCGGTT... |
Task1_train_45777 | A variant affecting Chromosome 17 has been observed. Determine if it's benign or associated with disease. | Benign | TTTAAATTTGATGAAGTCCATCTATTTTGTTGCTTATGCTTTTGATGTTAGATTTAAGAAGCCATTGACTAATTCAAGGCCATGAAAATTTACACCTACATTTCCTTCTAAGAAATGTATAGTTTTAGTGCTTCTTACCTTTAAGTCTTTGATCCATTTTGACTTAAATTTGTGTATGGTGTAAGGGAGCAGGTCCCATGTCATACCTGTGAGTAGCCAGTTGTCCCAGACCATTTTGCTTTGTTGTTGAGACAGGGTCTCGCTCTGTTGCCAAGACTGGAGTGCAGGGGTGTGATCATGGCTCACTGCAGCCTCGACCT... | TTTAAATTTGATGAAGTCCATCTATTTTGTTGCTTATGCTTTTGATGTTAGATTTAAGAAGCCATTGACTAATTCAAGGCCATGAAAATTTACACCTACATTTCCTTCTAAGAAATGTATAGTTTTAGTGCTTCTTACCTTTAAGTCTTTGATCCATTTTGACTTAAATTTGTGTATGGTGTAAGGGAGCAGGTCCCATGTCATACCTGTGAGTAGCCAGTTGTCCCAGACCATTTTGCTTTGTTGTTGAGACAGGGTCTCGCTCTGTTGCCAAGACTGGAGTGCAGGGGTGTGATCATGGCTCACTGCAGCCTCGACCT... |
Task1_train_45778 | Consider a variant on Chromosome 17. Determine its clinical classification and disease relevance. | Benign | TACCTTTAAGTCTTTGATCCATTTTGACTTAAATTTGTGTATGGTGTAAGGGAGCAGGTCCCATGTCATACCTGTGAGTAGCCAGTTGTCCCAGACCATTTTGCTTTGTTGTTGAGACAGGGTCTCGCTCTGTTGCCAAGACTGGAGTGCAGGGGTGTGATCATGGCTCACTGCAGCCTCGACCTCTTGGGCTCAAGCAATCCTCCTGGCTCAGCCTCCAGAGTAGCTGGGACTACAAGCATGTGCCACCATGCCTGGCTAATTTTTTTTTTTGAGACAGAGTCTCGCTGTGTCGCCCAGGCTGGTGTGCGGTGGCGTGA... | TACCTTTAAGTCTTTGATCCATTTTGACTTAAATTTGTGTATGGTGTAAGGGAGCAGGTCCCATGTCATACCTGTGAGTAGCCAGTTGTCCCAGACCATTTTGCTTTGTTGTTGAGACAGGGTCTCGCTCTGTTGCCAAGACTGGAGTGCAGGGGTGTGATCATGGCTCACTGCAGCCTCGACCTCTTGGGCTCAAGCAATCCTCCTGGCTCAGCCTCCAGAGTAGCTGGGACTACAAGCATGTGCCACCATGCCTGGCTAATTTTTTTTTTTGAGACAGAGTCTCGCTGTGTCGCCCAGGCTGGTGTGCGGTGGCGTGA... |
Task1_train_45779 | A mutation on Chromosome 17 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GCTGGGAGTACTCTGGGCGCCAGGGCTCCCCAAGGTGACTGCTCTAGGATGCCGCCACACTCTCAGGTGAGTAAGTGTCCTCACAGCTCAGGTTCCAGGCCTGGTGGCCTCCCTTTCCACAAGGCCCACCTTCTCCCTCCCCACCGGCCACTTCTCCCGTAAGCGCCAACCCCCATAGCCCATCTATATACTGTGGCACCCTGGGTATGGTGTGACTGACTCCAGGCAAAACATTCCTGGCCAGCAATGGGCACAGTAGCAGGCCCAGAGCCCAGGAACACACACCCCTTGGTCAATCCCTGGGTGAGCAGCCGTGGTCC... | GCTGGGAGTACTCTGGGCGCCAGGGCTCCCCAAGGTGACTGCTCTAGGATGCCGCCACACTCTCAGGTGAGTAAGTGTCCTCACAGCTCAGGTTCCAGGCCTGGTGGCCTCCCTTTCCACAAGGCCCACCTTCTCCCTCCCCACCGGCCACTTCTCCCGTAAGCGCCAACCCCCATAGCCCATCTATATACTGTGGCACCCTGGGTATGGTGTGACTGACTCCAGGCAAAACATTCCTGGCCAGCAATGGGCACAGTAGCAGGCCCAGAGCCCAGGAACACACACCCCTTGGTCAATCCCTGGGTGAGCAGCCGTGGTCC... |
Task1_train_45780 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | TCTTTGTACTCATCTGTTTGGTATGTGAGGGGTTTTGCGTTTTGTCTTCTGCTCTGTAATTTAAAGGGATAAAACGCTCACATTTAACTTAAGCCAAAACCCAGTTTCAGTCTTTCCACCAGAAATCCCTGAGATGTAGAATTGTGGGAAGCTCCTTGGAGGCTGGCGGGCTGCTGGGCTGCCCCTCTGTGGGAAGACAGCCTGCAGGCTTCAGTGGGCTGGGCTCTCCCGGCCATGGCTGCCTTGGTGGCTAACTCAGGCTGCGGCGACAGACTGGTGAGGCAGGCGGACTCTTCCCCTGATGTTTAATATAACCTGAC... | TCTTTGTACTCATCTGTTTGGTATGTGAGGGGTTTTGCGTTTTGTCTTCTGCTCTGTAATTTAAAGGGATAAAACGCTCACATTTAACTTAAGCCAAAACCCAGTTTCAGTCTTTCCACCAGAAATCCCTGAGATGTAGAATTGTGGGAAGCTCCTTGGAGGCTGGCGGGCTGCTGGGCTGCCCCTCTGTGGGAAGACAGCCTGCAGGCTTCAGTGGGCTGGGCTCTCCCGGCCATGGCTGCCTTGGTGGCTAACTCAGGCTGCGGCGACAGACTGGTGAGGCAGGCGGACTCTTCCCCTGATGTTTAATATAACCTGAC... |
Task1_train_45781 | This alteration on Chromosome 17 may affect genome function. Does it lead to a disease or is it benign? | Benign | TCAGTCTTTCCACCAGAAATCCCTGAGATGTAGAATTGTGGGAAGCTCCTTGGAGGCTGGCGGGCTGCTGGGCTGCCCCTCTGTGGGAAGACAGCCTGCAGGCTTCAGTGGGCTGGGCTCTCCCGGCCATGGCTGCCTTGGTGGCTAACTCAGGCTGCGGCGACAGACTGGTGAGGCAGGCGGACTCTTCCCCTGATGTTTAATATAACCTGACAGATAAAGTGGATTGTAATGAAGAAATTATCTAAAACCCATTTCTATTTCTTTGTTTGAAAAGAAAACATGGCCTTGAATATGATTCTTGGAGAAAAAGAAGAGAC... | TCAGTCTTTCCACCAGAAATCCCTGAGATGTAGAATTGTGGGAAGCTCCTTGGAGGCTGGCGGGCTGCTGGGCTGCCCCTCTGTGGGAAGACAGCCTGCAGGCTTCAGTGGGCTGGGCTCTCCCGGCCATGGCTGCCTTGGTGGCTAACTCAGGCTGCGGCGACAGACTGGTGAGGCAGGCGGACTCTTCCCCTGATGTTTAATATAACCTGACAGATAAAGTGGATTGTAATGAAGAAATTATCTAAAACCCATTTCTATTTCTTTGTTTGAAAAGAAAACATGGCCTTGAATATGATTCTTGGAGAAAAAGAAGAGAC... |
Task1_train_45782 | Chromosome 17 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GGACAACGAGGAGTGACTCTACTGTGGGCGTTGTTTCTGCCCCTGCAGCCGGGGCTGTGAGGCTGCAGGCTGCCCTTTGCTGGTTTGCAGGGGCCATAATTCTGGCCTGGAGCTTGACAAACGACCCAGGACCTCTGAGATGGGAAATGAGGTCTGCATCCCGTGTTCTAATCAGGATTCGCTATCAAAGGTCATTTTCCACACTGTGGCTTAATAGAGTTGGTTTTATATTCCCTGAGGGATACAGACTTCCAAATTGTTGCAGTCTCACTAACTGTAATGTATACAGCTCATGTTTGAAAGGAAATCGCCTCTCCTCC... | GGACAACGAGGAGTGACTCTACTGTGGGCGTTGTTTCTGCCCCTGCAGCCGGGGCTGTGAGGCTGCAGGCTGCCCTTTGCTGGTTTGCAGGGGCCATAATTCTGGCCTGGAGCTTGACAAACGACCCAGGACCTCTGAGATGGGAAATGAGGTCTGCATCCCGTGTTCTAATCAGGATTCGCTATCAAAGGTCATTTTCCACACTGTGGCTTAATAGAGTTGGTTTTATATTCCCTGAGGGATACAGACTTCCAAATTGTTGCAGTCTCACTAACTGTAATGTATACAGCTCATGTTTGAAAGGAAATCGCCTCTCCTCC... |
Task1_train_45783 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | CCCAGGGTCTTGGCTTCATCCACAGACGGCTGGGTTGAAGGGGTGGTTTGGAGCCTCATGCTGCCCACTAGGCTGTGCCAGCTGTGCACCACCCTGCTCCCCACCCTCCGGGAGCAGCCATCCCCTTCCCCTGCCAGTGCGCCCCTCCCCAGGGCAGGTTTCAGCCATGTCTGCCCTGGAGATGAAGGTTCCCCGTCCATGCAGTGCACCCAGCACCACCTGCGTGCGCCCGTGGGAAAGGATGACCACAGCCCCTCGGCCAGGAGGATGTTAAGGGCGGTCTTGAGTTCCAGGCCCCGTCACAGTCCAGGCAGCAGAGC... | CCCAGGGTCTTGGCTTCATCCACAGACGGCTGGGTTGAAGGGGTGGTTTGGAGCCTCATGCTGCCCACTAGGCTGTGCCAGCTGTGCACCACCCTGCTCCCCACCCTCCGGGAGCAGCCATCCCCTTCCCCTGCCAGTGCGCCCCTCCCCAGGGCAGGTTTCAGCCATGTCTGCCCTGGAGATGAAGGTTCCCCGTCCATGCAGTGCACCCAGCACCACCTGCGTGCGCCCGTGGGAAAGGATGACCACAGCCCCTCGGCCAGGAGGATGTTAAGGGCGGTCTTGAGTTCCAGGCCCCGTCACAGTCCAGGCAGCAGAGC... |
Task1_train_45784 | Mutation context: Chromosome 17. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TTCATCCACAGACGGCTGGGTTGAAGGGGTGGTTTGGAGCCTCATGCTGCCCACTAGGCTGTGCCAGCTGTGCACCACCCTGCTCCCCACCCTCCGGGAGCAGCCATCCCCTTCCCCTGCCAGTGCGCCCCTCCCCAGGGCAGGTTTCAGCCATGTCTGCCCTGGAGATGAAGGTTCCCCGTCCATGCAGTGCACCCAGCACCACCTGCGTGCGCCCGTGGGAAAGGATGACCACAGCCCCTCGGCCAGGAGGATGTTAAGGGCGGTCTTGAGTTCCAGGCCCCGTCACAGTCCAGGCAGCAGAGCCCATTTTGCCACTG... | TTCATCCACAGACGGCTGGGTTGAAGGGGTGGTTTGGAGCCTCATGCTGCCCACTAGGCTGTGCCAGCTGTGCACCACCCTGCTCCCCACCCTCCGGGAGCAGCCATCCCCTTCCCCTGCCAGTGCGCCCCTCCCCAGGGCAGGTTTCAGCCATGTCTGCCCTGGAGATGAAGGTTCCCCGTCCATGCAGTGCACCCAGCACCACCTGCGTGCGCCCGTGGGAAAGGATGACCACAGCCCCTCGGCCAGGAGGATGTTAAGGGCGGTCTTGAGTTCCAGGCCCCGTCACAGTCCAGGCAGCAGAGCCCATTTTGCCACTG... |
Task1_train_45785 | Chromosome 17 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GGTTCCCCGTCCATGCAGTGCACCCAGCACCACCTGCGTGCGCCCGTGGGAAAGGATGACCACAGCCCCTCGGCCAGGAGGATGTTAAGGGCGGTCTTGAGTTCCAGGCCCCGTCACAGTCCAGGCAGCAGAGCCCATTTTGCCACTGGAGAGAGCCCAAGCCCCCTGCAGTCATTCTCTGACAGTTTCTGTGGCCTCCTGAAGCACACGGGGGTGTAAACAGTGGCCTGCGTGGAGGCCTCAGGCTGCTGGTGGCTTTCCACCCCGTGCCCACCGGCCAGGTCCCGGGTGGATGAAGCACTCCCTGACCCTCCGTGAAT... | GGTTCCCCGTCCATGCAGTGCACCCAGCACCACCTGCGTGCGCCCGTGGGAAAGGATGACCACAGCCCCTCGGCCAGGAGGATGTTAAGGGCGGTCTTGAGTTCCAGGCCCCGTCACAGTCCAGGCAGCAGAGCCCATTTTGCCACTGGAGAGAGCCCAAGCCCCCTGCAGTCATTCTCTGACAGTTTCTGTGGCCTCCTGAAGCACACGGGGGTGTAAACAGTGGCCTGCGTGGAGGCCTCAGGCTGCTGGTGGCTTTCCACCCCGTGCCCACCGGCCAGGTCCCGGGTGGATGAAGCACTCCCTGACCCTCCGTGAAT... |
Task1_train_45786 | This is a variant located on Chromosome 17. Is this mutation a likely cause of disease or not? | Benign | ACAAGAAGAGAAAAATGCAGGTTAGAGAACAGGCCTGCACCAGTGGAGGGCTTCCTACCCCTGCAGCTCCCCGTGGGGTCCAGGCAAGCGATGTGCCTTTGCCACTGACTTTCTGATGAGAATCGGCTGTGATTCGGGGCAGGAGTGAGAACCACGCGGCTGCACTGCCCTCGGCTGTGGTCTGGGCCAGATCTAGGACCCTTCTCTGGGAACCCACTTTTTTTTTTTTTTTTTTTTTTTTGAGACAGGGTCTTACTCTGTCACCCAGGCTGGAGTGCAGTGGTGGGAACACAGCTCACTACTGCCTCGCCCTCCTGGGT... | ACAAGAAGAGAAAAATGCAGGTTAGAGAACAGGCCTGCACCAGTGGAGGGCTTCCTACCCCTGCAGCTCCCCGTGGGGTCCAGGCAAGCGATGTGCCTTTGCCACTGACTTTCTGATGAGAATCGGCTGTGATTCGGGGCAGGAGTGAGAACCACGCGGCTGCACTGCCCTCGGCTGTGGTCTGGGCCAGATCTAGGACCCTTCTCTGGGAACCCACTTTTTTTTTTTTTTTTTTTTTTTTGAGACAGGGTCTTACTCTGTCACCCAGGCTGGAGTGCAGTGGTGGGAACACAGCTCACTACTGCCTCGCCCTCCTGGGT... |
Task1_train_45787 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | GGGGCCATGCCTCGTCCTGGTTTAAGTGTCCTGTGAGCACACCGGAGGAGCTGCCGGATGGGGCATGCGGGTCCTCCGAGGCCAGGCAGGCAGGGCAGAGGGTGGGGGCCGCCGTGCCCAGGGGCACTGGCCCCTTTTGAGTGTGTATGTGTGTACAGACACCCACTGTGGCTCCAGGCGCCCCCAGGGGCTAGCAGCAAGCCTAAAAGCCCAGACGAATTCTGCCTCTGGGGCGGAGCATGGCCGATCTACCATCCAGGGCCTCTCATCCCACGGGCTTCTCCAGGACACCGCGTGGGGCAGAGGCACCTGAATCTGCT... | GGGGCCATGCCTCGTCCTGGTTTAAGTGTCCTGTGAGCACACCGGAGGAGCTGCCGGATGGGGCATGCGGGTCCTCCGAGGCCAGGCAGGCAGGGCAGAGGGTGGGGGCCGCCGTGCCCAGGGGCACTGGCCCCTTTTGAGTGTGTATGTGTGTACAGACACCCACTGTGGCTCCAGGCGCCCCCAGGGGCTAGCAGCAAGCCTAAAAGCCCAGACGAATTCTGCCTCTGGGGCGGAGCATGGCCGATCTACCATCCAGGGCCTCTCATCCCACGGGCTTCTCCAGGACACCGCGTGGGGCAGAGGCACCTGAATCTGCT... |
Task1_train_45788 | A mutation is present on Chromosome 17. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CTCGCAGAAGGTCTCGGACAGCAGGCTGGGCATCTTGAGCAGGCTGCGCAGGTTGCGCGCGCTCTGGCTCTCAGCCACCACCACGGGCACCGCCGGCGCCTCCTCTTCGCTGTCCTCGCTAGGCTCCTGGACGCTGTAGCAGCGGAGCTCCTCGTCAGACTCGTCGCTGTCCTCACTGTCCTCCTCCTCCTCCTCCGGCCGGCCCTCCAAGGCCGCAGGGAGGCCGGGCAGAGCCAGGCGGAGTGGGGCTCTGGGGGTGCCTGGGCCCCCCATCCGCTTTTGTGGGGCCGGCCCTGACAACAGTCCTGGGGGCCCCTGGA... | CTCGCAGAAGGTCTCGGACAGCAGGCTGGGCATCTTGAGCAGGCTGCGCAGGTTGCGCGCGCTCTGGCTCTCAGCCACCACCACGGGCACCGCCGGCGCCTCCTCTTCGCTGTCCTCGCTAGGCTCCTGGACGCTGTAGCAGCGGAGCTCCTCGTCAGACTCGTCGCTGTCCTCACTGTCCTCCTCCTCCTCCTCCGGCCGGCCCTCCAAGGCCGCAGGGAGGCCGGGCAGAGCCAGGCGGAGTGGGGCTCTGGGGGTGCCTGGGCCCCCCATCCGCTTTTGTGGGGCCGGCCCTGACAACAGTCCTGGGGGCCCCTGGA... |
Task1_train_45789 | A variant was discovered on Chromosome 17. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GCAGGGCCCAAGGACAGCTTGTGTGGCGTCCCGCAGCCTCCCCCGGCCGGACATCCCAGCTCACTGGGATCCCATTAAACTCCAGCCCGGGCCGCGGATGCACGAGCTATAAATAAACCAGCAGCCTGGAGCTCCAGGCCTGCCTCCCACCCTGTCTCCAGCCCGGATCTCGGGCTCCCCTGCCTTCGTTGGGGGCACCCCTGAGAGCAGTGGGATTGGGGGTGGTGAACGAGCCCAGCCCAGGGGCACCCCCAGCACTGGGCAGATGGGACATTGGTTCCTGGCTTGGCCACATTTAGCCTGGAATTCGGCCCAGCCCC... | GCAGGGCCCAAGGACAGCTTGTGTGGCGTCCCGCAGCCTCCCCCGGCCGGACATCCCAGCTCACTGGGATCCCATTAAACTCCAGCCCGGGCCGCGGATGCACGAGCTATAAATAAACCAGCAGCCTGGAGCTCCAGGCCTGCCTCCCACCCTGTCTCCAGCCCGGATCTCGGGCTCCCCTGCCTTCGTTGGGGGCACCCCTGAGAGCAGTGGGATTGGGGGTGGTGAACGAGCCCAGCCCAGGGGCACCCCCAGCACTGGGCAGATGGGACATTGGTTCCTGGCTTGGCCACATTTAGCCTGGAATTCGGCCCAGCCCC... |
Task1_train_45790 | A change on Chromosome 17 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GTGGTTGGGGCATGAGTGTTCACCTCTGCCCAGGAAGGTCTCGGACTACATGAATGCCTGAAGTTATGGCTCTCTCAAAAGAAGCCCTGGCCGCAGCACCCACCCCACACCTGGCCGGCTCATGGGAGGGGAGGGCCCACCTCGGACAGTGACCTCCTTGATCTTCTTGGTTTTCTCACTGATCCACTTCTCCCGGCGGGCTTTCTCGGTGGCGCTCATTAATTCTTTGAGTTTTTTAATCTCCTACGAGCAGAACAGGGCAGGAGGAAACGACACGAAGGACACCCCCGTCCCTTTGCCACCCTGTGGGCACAGTCAGG... | GTGGTTGGGGCATGAGTGTTCACCTCTGCCCAGGAAGGTCTCGGACTACATGAATGCCTGAAGTTATGGCTCTCTCAAAAGAAGCCCTGGCCGCAGCACCCACCCCACACCTGGCCGGCTCATGGGAGGGGAGGGCCCACCTCGGACAGTGACCTCCTTGATCTTCTTGGTTTTCTCACTGATCCACTTCTCCCGGCGGGCTTTCTCGGTGGCGCTCATTAATTCTTTGAGTTTTTTAATCTCCTACGAGCAGAACAGGGCAGGAGGAAACGACACGAAGGACACCCCCGTCCCTTTGCCACCCTGTGGGCACAGTCAGG... |
Task1_train_45791 | Here’s a variant located on Chromosome 17. What is the predicted biological effect — harmless or disease-causing? | Benign | TGCTCCATTTAGCCTGGCCGCTAGTGTTCACCCAGGACAAACCAACCCAGAGGACAGCAGGGCTCCAGAGGGCTGAACTATCCACACATATGGGCTCGTGGAGGCAGCTCGGGGCAGCGGGTAGGTGGGGGCAGTATGGGGAATGCGGGCCCTGCCACCTCCACCCTGAGAGACCCGTGGGGGGTGCTGCATAACTAGGTGGGTACATGGTGAGGGACCACCTCCTGCTGGGGGCCGGGTGGGGGCTGGCGAGAGACCTCCTCCCCCTGGGGGCCAGGTGCGGGCTGGTGAGGGGCCTCCTCCCCCGAGGGCCAGGTGCA... | TGCTCCATTTAGCCTGGCCGCTAGTGTTCACCCAGGACAAACCAACCCAGAGGACAGCAGGGCTCCAGAGGGCTGAACTATCCACACATATGGGCTCGTGGAGGCAGCTCGGGGCAGCGGGTAGGTGGGGGCAGTATGGGGAATGCGGGCCCTGCCACCTCCACCCTGAGAGACCCGTGGGGGGTGCTGCATAACTAGGTGGGTACATGGTGAGGGACCACCTCCTGCTGGGGGCCGGGTGGGGGCTGGCGAGAGACCTCCTCCCCCTGGGGGCCAGGTGCGGGCTGGTGAGGGGCCTCCTCCCCCGAGGGCCAGGTGCA... |
Task1_train_45792 | Consider this mutation on Chromosome 17. Is this a benign change or a disease-causing variant? | Benign | GCCTGGGTCGGCCGCGGATAGAGCCTGGCCATGCCGCCGAAAGACCATCTACTAGAAAGCCCGGAAACTTTTACAACAGTCTCCACACAACAAGAGAGCTGCAATTTCTTTCTTTCTCCTTCTCCCTCTCCCTCTCCCTCCCCCTCCCCCTCCCTCTTTCTTTCTTTCTTTCTTTTTTTGAGACAGAGTCTTGCTCTTTCGCCCAGGCTGGAGTACAGTGGCATGATCTCGGCTCACTGCAGCCTCCTCCGCCCGGGTTCAAGCAACTCTCCTGTCTCAGCCTCCTGAGTAGCTGGGATTAAGGGTGCGCGCCACCACGC... | GCCTGGGTCGGCCGCGGATAGAGCCTGGCCATGCCGCCGAAAGACCATCTACTAGAAAGCCCGGAAACTTTTACAACAGTCTCCACACAACAAGAGAGCTGCAATTTCTTTCTTTCTCCTTCTCCCTCTCCCTCTCCCTCCCCCTCCCCCTCCCTCTTTCTTTCTTTCTTTCTTTTTTTGAGACAGAGTCTTGCTCTTTCGCCCAGGCTGGAGTACAGTGGCATGATCTCGGCTCACTGCAGCCTCCTCCGCCCGGGTTCAAGCAACTCTCCTGTCTCAGCCTCCTGAGTAGCTGGGATTAAGGGTGCGCGCCACCACGC... |
Task1_train_45793 | Given a variant located on Chromosome 17, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GGCCGAGGGAAACGGGATTTCTTTGCTTCCCGCACGGAAAAGATCCATCCAAGCGGGTAAGAGGGAAGCGAAGCTTGCATTTTTTATGTTGAAAAAAAAATTCAAAATGGAAAATCATTTTATTGGTCACCACCCATAAGTAAACTAAAAACAGGGATAATTAGAGTGTGGGGATTTGGAGGGACCATAAATCTGCGGCGCCTTTTCCACTGGAATCAGGAGCCTTTATGGCTTGTTGTTTTATTTTGAGAGAAATGAGATCCCTGGCTTTGGTGCAGGCGGGTGTGCGCTCCGAGCGTCTTTCGGCGGGGGGGAGGGGG... | GGCCGAGGGAAACGGGATTTCTTTGCTTCCCGCACGGAAAAGATCCATCCAAGCGGGTAAGAGGGAAGCGAAGCTTGCATTTTTTATGTTGAAAAAAAAATTCAAAATGGAAAATCATTTTATTGGTCACCACCCATAAGTAAACTAAAAACAGGGATAATTAGAGTGTGGGGATTTGGAGGGACCATAAATCTGCGGCGCCTTTTCCACTGGAATCAGGAGCCTTTATGGCTTGTTGTTTTATTTTGAGAGAAATGAGATCCCTGGCTTTGGTGCAGGCGGGTGTGCGCTCCGAGCGTCTTTCGGCGGGGGGGAGGGGG... |
Task1_train_45794 | This mutation is located on Chromosome 17. Is it associated with a disease or is it a benign polymorphism? | Benign | CGGACTGTGCCCGCAGCAGGGAGCACGACACCACGCACGGCGACGGGGAGGTGCGGCAGCCCCCTGTGGGCATTGCAGTGGCCTTGGCCCGGCAGAAGGACACAGTGAGCCGGTCTGAGGCAGCCTACGGCACCAACACTGCGCGGCAGGGCCGGGCCGCCCCCGCCTTCAAAGGTACAGGCCCTGCACAGAGAGGGAGGCAGGCCGGGACAGTCTAGGGGGCCCAGCTGGCCCTGCCCTGCGCCCCGGCTCCCCAGCTCCCACACCTGCCCTTGGCAGACCCTCCGAGGCCCCAGGACCAGGGGATCCTCCTCAGTGCA... | CGGACTGTGCCCGCAGCAGGGAGCACGACACCACGCACGGCGACGGGGAGGTGCGGCAGCCCCCTGTGGGCATTGCAGTGGCCTTGGCCCGGCAGAAGGACACAGTGAGCCGGTCTGAGGCAGCCTACGGCACCAACACTGCGCGGCAGGGCCGGGCCGCCCCCGCCTTCAAAGGTACAGGCCCTGCACAGAGAGGGAGGCAGGCCGGGACAGTCTAGGGGGCCCAGCTGGCCCTGCCCTGCGCCCCGGCTCCCCAGCTCCCACACCTGCCCTTGGCAGACCCTCCGAGGCCCCAGGACCAGGGGATCCTCCTCAGTGCA... |
Task1_train_45795 | This sequence variant lies on Chromosome 17. Is it clinically significant, and what condition might it cause if any? | Benign | GGCCGGACCTGGCTCCAGGAGACCCCTGCATGCCTGGCCTCTGGCAGGATGAACCCAAGCAGGGGGCCCACTGGGGTCAGGGGATCCTGAGCCTGACCGAGCTTGCCCCCATCCCTGACAGCGGAAGCCCGAAGACCAGCACCTGGATCTGGAGGAGCCCGCCCAGGAGAAGGCCCCAAAGTCCACCCACAAGCCAGTTGCCTTAACCCCCACGGCCCCGGGCGCCCCCTCACCCGCTGCAGGCCCCACCAAGCTGCCACCTTGCTGCCATCCGCCCGACCCAAAGCCCCCCGCCAGCTCCCCCACCCCACCACCTCGGC... | GGCCGGACCTGGCTCCAGGAGACCCCTGCATGCCTGGCCTCTGGCAGGATGAACCCAAGCAGGGGGCCCACTGGGGTCAGGGGATCCTGAGCCTGACCGAGCTTGCCCCCATCCCTGACAGCGGAAGCCCGAAGACCAGCACCTGGATCTGGAGGAGCCCGCCCAGGAGAAGGCCCCAAAGTCCACCCACAAGCCAGTTGCCTTAACCCCCACGGCCCCGGGCGCCCCCTCACCCGCTGCAGGCCCCACCAAGCTGCCACCTTGCTGCCATCCGCCCGACCCAAAGCCCCCCGCCAGCTCCCCCACCCCACCACCTCGGC... |
Task1_train_45796 | A genomic change on Chromosome 17 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CCCGTGCACTTTAAATGTCTGCCCTGCCAGCAGCCCCGGGCCTGGCTCCCGGGTGCGCAGCGCCGAGGAAAAGAATGGGGAGGGTCAGCAGTCCACGGCCGACATCATCACATCCGAACCAGGTGAGAGTAGCCGCCTGGCCCGGCCCACTGTGCTCCGCTCCAAGCCCTCCCACCCCTGCCCGGCAGGGCTGCGCTGAATCCGGGCTGCCTGCAGGGAGGCGCCACACCTGCCCAGACCCAGGGCAGCATGGCTGTTCCCTTCCTCTCTCTTCCCTCTTCCCAGTCCTCCCAATGACCTTGGGAGAAGCACACAGTGCC... | CCCGTGCACTTTAAATGTCTGCCCTGCCAGCAGCCCCGGGCCTGGCTCCCGGGTGCGCAGCGCCGAGGAAAAGAATGGGGAGGGTCAGCAGTCCACGGCCGACATCATCACATCCGAACCAGGTGAGAGTAGCCGCCTGGCCCGGCCCACTGTGCTCCGCTCCAAGCCCTCCCACCCCTGCCCGGCAGGGCTGCGCTGAATCCGGGCTGCCTGCAGGGAGGCGCCACACCTGCCCAGACCCAGGGCAGCATGGCTGTTCCCTTCCTCTCTCTTCCCTCTTCCCAGTCCTCCCAATGACCTTGGGAGAAGCACACAGTGCC... |
Task1_train_45797 | With a mutation on Chromosome 17, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CTTTGGTGGAATCTCAGGTGCGTGCCCCAGCTGTCAGGCGCTGATTTGTCCCATCGTGGATGGGGTTCTCCCGCACTCCTGCTTCTGGCTGAGATGAGCCATATCTCTGGGGAGCCCCGGTCCGTTAAGTGGAGCGTGGGGTTCTGAGGCAGAGACTAGGTTTGGGGTGCTCGTTGCTGTGAGGTTATCGTTGCTCCTGGGCTTTCCCAGGGGATACCAGCACCTCTACTCACCCCACAGGGGTTCCGCAGTTCTCCTGCCTTCCTGGCCATCACCACCCACCCCCACCGCAAGGTGTCTGGCTCCTGTCTCCTGCTGGA... | CTTTGGTGGAATCTCAGGTGCGTGCCCCAGCTGTCAGGCGCTGATTTGTCCCATCGTGGATGGGGTTCTCCCGCACTCCTGCTTCTGGCTGAGATGAGCCATATCTCTGGGGAGCCCCGGTCCGTTAAGTGGAGCGTGGGGTTCTGAGGCAGAGACTAGGTTTGGGGTGCTCGTTGCTGTGAGGTTATCGTTGCTCCTGGGCTTTCCCAGGGGATACCAGCACCTCTACTCACCCCACAGGGGTTCCGCAGTTCTCCTGCCTTCCTGGCCATCACCACCCACCCCCACCGCAAGGTGTCTGGCTCCTGTCTCCTGCTGGA... |
Task1_train_45798 | A variant found on Chromosome 17 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GACACGGGCACAAGCGCTGTACAAAGGTCAGAGCCAGAAGCTCCTGCCCACGGGTGGCAGAGGACAGCCCTGGAGCACAGCAGGGATGGGACCGTTAAGGGGTGCAGGCCTGCCTCGGTGGGTGGCTCGCTTGGCCCCAGCTCTCCCAGCAAGCACGGGGCCATGGCCCCATTGAAAAGGCTGGGTTTGGAGTGTCACCACCCACTGAAAATGCTGGGTTTGGACTGTCTCCACCCGCTGAAGAGGCCGGGTTTGGAGTGTCATCAGGGCGGCCGTGCTCCCTTAGATGTGGCAACCACTGAGGGAGACAAACCCTGACT... | GACACGGGCACAAGCGCTGTACAAAGGTCAGAGCCAGAAGCTCCTGCCCACGGGTGGCAGAGGACAGCCCTGGAGCACAGCAGGGATGGGACCGTTAAGGGGTGCAGGCCTGCCTCGGTGGGTGGCTCGCTTGGCCCCAGCTCTCCCAGCAAGCACGGGGCCATGGCCCCATTGAAAAGGCTGGGTTTGGAGTGTCACCACCCACTGAAAATGCTGGGTTTGGACTGTCTCCACCCGCTGAAGAGGCCGGGTTTGGAGTGTCATCAGGGCGGCCGTGCTCCCTTAGATGTGGCAACCACTGAGGGAGACAAACCCTGACT... |
Task1_train_45799 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | AGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCAGACGTTGCAGTGAGTCAAAATCGCACCACTGGACTCCAGCCTGGAGACAGAGCGAGACCTTGTCTCAAAGAAAACCAAAACCAAGTGCAGACTCTGAGCCCCAGGCAGCCTTGCCCATCCTCAGGGACACACGTGTCCTGGCAGCCTGGGCTACCCTGCAAGCGCCTTTGCTGGTGGGACTTGAGAGTGTGCTGGAGGCACCACAGTCCTGAGTCTCTGGAAAGGTGTGCACGACAGGGGCTGGAGACCAGCAGTGCCATTTGCCATTCAGC... | AGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCAGACGTTGCAGTGAGTCAAAATCGCACCACTGGACTCCAGCCTGGAGACAGAGCGAGACCTTGTCTCAAAGAAAACCAAAACCAAGTGCAGACTCTGAGCCCCAGGCAGCCTTGCCCATCCTCAGGGACACACGTGTCCTGGCAGCCTGGGCTACCCTGCAAGCGCCTTTGCTGGTGGGACTTGAGAGTGTGCTGGAGGCACCACAGTCCTGAGTCTCTGGAAAGGTGTGCACGACAGGGGCTGGAGACCAGCAGTGCCATTTGCCATTCAGC... |
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