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_41400 | A mutation has occurred on Chromosome 11. What is the medical relevance of this mutation? | Benign | CCGTTCTTTCTTTCCCTCCAGGCGAAGTCCGCCTCGTCAGTTTGCACATCCAGGCTCTGGTGGACGCTGGTGTTCCAGCCCGTGACATTGCTGTGGTCTCGCCATACAACCTCCAGGTACGAGGGTTTCCTTTTGTCCCTCTACAGAGCAGCTGGGGCTCACACAACCTAGAGGGTGAAAGAAAAAGGGTGATTTGTTGGCTGTGGTGACCGAAAAGTTCAGGGGTAGGGCTGACCTTATTGTGACTGGATCCAGGGCCCAAATGATGTCGTCAGGGGCCCCTCTGCGTGTTCGTCTGCCCGCCCCACCTTGCCCCGCCC... | CCGTTCTTTCTTTCCCTCCAGGCGAAGTCCGCCTCGTCAGTTTGCACATCCAGGCTCTGGTGGACGCTGGTGTTCCAGCCCGTGACATTGCTGTGGTCTCGCCATACAACCTCCAGGTACGAGGGTTTCCTTTTGTCCCTCTACAGAGCAGCTGGGGCTCACACAACCTAGAGGGTGAAAGAAAAAGGGTGATTTGTTGGCTGTGGTGACCGAAAAGTTCAGGGGTAGGGCTGACCTTATTGTGACTGGATCCAGGGCCCAAATGATGTCGTCAGGGGCCCCTCTGCGTGTTCGTCTGCCCGCCCCACCTTGCCCCGCCC... |
Task1_train_41401 | A mutation found on Chromosome 11 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GTGTTCCAGCCCGTGACATTGCTGTGGTCTCGCCATACAACCTCCAGGTACGAGGGTTTCCTTTTGTCCCTCTACAGAGCAGCTGGGGCTCACACAACCTAGAGGGTGAAAGAAAAAGGGTGATTTGTTGGCTGTGGTGACCGAAAAGTTCAGGGGTAGGGCTGACCTTATTGTGACTGGATCCAGGGCCCAAATGATGTCGTCAGGGGCCCCTCTGCGTGTTCGTCTGCCCGCCCCACCTTGCCCCGCCCTGCCCGGTGCCCCAGCCTTCTGCACTGGCTTGTGTTCTGGCCAGATTTGCTGGGTGACCCCGGCAGCCT... | GTGTTCCAGCCCGTGACATTGCTGTGGTCTCGCCATACAACCTCCAGGTACGAGGGTTTCCTTTTGTCCCTCTACAGAGCAGCTGGGGCTCACACAACCTAGAGGGTGAAAGAAAAAGGGTGATTTGTTGGCTGTGGTGACCGAAAAGTTCAGGGGTAGGGCTGACCTTATTGTGACTGGATCCAGGGCCCAAATGATGTCGTCAGGGGCCCCTCTGCGTGTTCGTCTGCCCGCCCCACCTTGCCCCGCCCTGCCCGGTGCCCCAGCCTTCTGCACTGGCTTGTGTTCTGGCCAGATTTGCTGGGTGACCCCGGCAGCCT... |
Task1_train_41402 | A variant on Chromosome 11 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GTTACTGATAAGGGCGTAGGAGCCTGACTGTGTTTCTTAGTCTGAAACCTGCTTCTCACTCCCCTCTGGCCTTTTGTAGGTGAAGTTGGTTTTCTTGCTGAGGACCGGAGGATCAACGTGGCTGTCACCCGTGCCCGACGCCACGTGGCGGTCATCTGTGACTCCCGTACTGTCAACAACCATGCATTTTTGAAGACCCTGGTGGAGTATTTCACACAGCATGGGGAAGTACGCACGGCCTTTGAGTATCTTGACGATATTGTCCCAGAAAACTATTCCCATGAGAACTCCCAGGGTTCCAGCCACGCTGCCACCAAGCC... | GTTACTGATAAGGGCGTAGGAGCCTGACTGTGTTTCTTAGTCTGAAACCTGCTTCTCACTCCCCTCTGGCCTTTTGTAGGTGAAGTTGGTTTTCTTGCTGAGGACCGGAGGATCAACGTGGCTGTCACCCGTGCCCGACGCCACGTGGCGGTCATCTGTGACTCCCGTACTGTCAACAACCATGCATTTTTGAAGACCCTGGTGGAGTATTTCACACAGCATGGGGAAGTACGCACGGCCTTTGAGTATCTTGACGATATTGTCCCAGAAAACTATTCCCATGAGAACTCCCAGGGTTCCAGCCACGCTGCCACCAAGCC... |
Task1_train_41403 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | GAAACTATTTGAAGAAATAAAATCACTTGTAAGTTACATTTAAAAAAAAACAACGAGTGGATCTCGGCCTTCCCCGGAGCTGGACCCTGTCCTCTAGTGGGATGGGAGGTGGCTTCCTGATGAGCCAGGGTTGCCCCTGGGGTTTCCAGATTGTGGGAAAGTCCAGGGGGTCCCTGGGGTGGAGGAGAGGCAGCAGCTATTTATCAAGCTGCAGGGAAGCATTTCAATACTTTAACTGTTGGTGTGGCTGTAAGAGTGCATCCCAGCTGAGTATCGGTCCTGCCCTCAGGGTCTAGGCTTGTGTATAAATGCATGCAGGT... | GAAACTATTTGAAGAAATAAAATCACTTGTAAGTTACATTTAAAAAAAAACAACGAGTGGATCTCGGCCTTCCCCGGAGCTGGACCCTGTCCTCTAGTGGGATGGGAGGTGGCTTCCTGATGAGCCAGGGTTGCCCCTGGGGTTTCCAGATTGTGGGAAAGTCCAGGGGGTCCCTGGGGTGGAGGAGAGGCAGCAGCTATTTATCAAGCTGCAGGGAAGCATTTCAATACTTTAACTGTTGGTGTGGCTGTAAGAGTGCATCCCAGCTGAGTATCGGTCCTGCCCTCAGGGTCTAGGCTTGTGTATAAATGCATGCAGGT... |
Task1_train_41404 | A genomic change on Chromosome 11 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GGTTTCCAGATTGTGGGAAAGTCCAGGGGGTCCCTGGGGTGGAGGAGAGGCAGCAGCTATTTATCAAGCTGCAGGGAAGCATTTCAATACTTTAACTGTTGGTGTGGCTGTAAGAGTGCATCCCAGCTGAGTATCGGTCCTGCCCTCAGGGTCTAGGCTTGTGTATAAATGCATGCAGGTGGGCCAGGTGCAAGGAACAGGTGAGAGGGAGCACAGTGGCAAATCTGAGAGCCCCTCTCTTGAGCGAAGCGGGCAGCCTGCTGTGCTCCAGCTGGTGGGGGCCAGGGATTGGGTGCACTGGAGTGGCTGATCGTCCTCCC... | GGTTTCCAGATTGTGGGAAAGTCCAGGGGGTCCCTGGGGTGGAGGAGAGGCAGCAGCTATTTATCAAGCTGCAGGGAAGCATTTCAATACTTTAACTGTTGGTGTGGCTGTAAGAGTGCATCCCAGCTGAGTATCGGTCCTGCCCTCAGGGTCTAGGCTTGTGTATAAATGCATGCAGGTGGGCCAGGTGCAAGGAACAGGTGAGAGGGAGCACAGTGGCAAATCTGAGAGCCCCTCTCTTGAGCGAAGCGGGCAGCCTGCTGTGCTCCAGCTGGTGGGGGCCAGGGATTGGGTGCACTGGAGTGGCTGATCGTCCTCCC... |
Task1_train_41405 | A mutation on Chromosome 11 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | ACTGTGGGTGGTGTGGTGGCCGTGGGTGGGCCCTTCTGTCCTCACAGAAGGAAGGCAGGGAAGATGGGGATATCTGTGAGAGTGTGTGTGTGTGAGTGTGAGTGTGTGTGTGAGTCTGTTTTGCGTGTCCATAAAGCAAGACCTGAGGCTGGGTATTAATAGAGAAGGGGTTTATTTGGCTCACGGCTCTGTAGGCTGCATGGGAAGCATGGTGCTGGCGTCTGCTTCTGATGAGGCCTCAGGAAGCATCCACTCATGGCAGAAGGAGACGGGGAGCAGGTGTGTCACATGGCGAGAGAGGCCCCCAGACTCCTTTTAAA... | ACTGTGGGTGGTGTGGTGGCCGTGGGTGGGCCCTTCTGTCCTCACAGAAGGAAGGCAGGGAAGATGGGGATATCTGTGAGAGTGTGTGTGTGTGAGTGTGAGTGTGTGTGTGAGTCTGTTTTGCGTGTCCATAAAGCAAGACCTGAGGCTGGGTATTAATAGAGAAGGGGTTTATTTGGCTCACGGCTCTGTAGGCTGCATGGGAAGCATGGTGCTGGCGTCTGCTTCTGATGAGGCCTCAGGAAGCATCCACTCATGGCAGAAGGAGACGGGGAGCAGGTGTGTCACATGGCGAGAGAGGCCCCCAGACTCCTTTTAAA... |
Task1_train_41406 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | ACCCCAGAGATCCCCCACCAACAGCTTCACCCGAGGGATCCCCCACCCCACGGCTTCACCCCAGGGATCTCCCGCCAACAGGTTCACCCCAGGGATCCCCCACCAACAGCTTCACCCCAGAGATCCCCCACCAACAGCTTCACCCGAGGGATCCCCCACCAACAGCTTCACCCCAGGGATCTCCCACCAGCAGCTTCACCCCAGGGATCCCTCACCAACAGCTTCACCCCAGGGATCCCCCACCAACAGCTTCACCCCAGGGATCCCTCACCAACAGCTTCACCCCAGGGATCCCCCACCCCACGGCTTCACCCCAGGGA... | ACCCCAGAGATCCCCCACCAACAGCTTCACCCGAGGGATCCCCCACCCCACGGCTTCACCCCAGGGATCTCCCGCCAACAGGTTCACCCCAGGGATCCCCCACCAACAGCTTCACCCCAGAGATCCCCCACCAACAGCTTCACCCGAGGGATCCCCCACCAACAGCTTCACCCCAGGGATCTCCCACCAGCAGCTTCACCCCAGGGATCCCTCACCAACAGCTTCACCCCAGGGATCCCCCACCAACAGCTTCACCCCAGGGATCCCTCACCAACAGCTTCACCCCAGGGATCCCCCACCCCACGGCTTCACCCCAGGGA... |
Task1_train_41407 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | CCACCAACAGCTTCACCCCAGGGATCCCTCACCAACAGCTTCACCCCAGGGATCCCCCACCCCACGGCTTCACCCCAGGGATCCCCCGCCAACAGGTTCACCCCAGGGATCCCCCACCAACAGCTTCACCCCGGGGATCCCCCACCAACAGCTTCACCCCAGGGATCCCCCACCAACAGCTTCACCCCAGGGATCCCCCATGCCACGGCTTCACCCCAGGGATCCCCCACCAACAGCTTCACCCCAGGGATCCCCCACCAACAGCTTCACCCCAGGGATCCCCCACCCCACACTTTCTGTTCTGTCCCCACCATTGACCT... | CCACCAACAGCTTCACCCCAGGGATCCCTCACCAACAGCTTCACCCCAGGGATCCCCCACCCCACGGCTTCACCCCAGGGATCCCCCGCCAACAGGTTCACCCCAGGGATCCCCCACCAACAGCTTCACCCCGGGGATCCCCCACCAACAGCTTCACCCCAGGGATCCCCCACCAACAGCTTCACCCCAGGGATCCCCCATGCCACGGCTTCACCCCAGGGATCCCCCACCAACAGCTTCACCCCAGGGATCCCCCACCAACAGCTTCACCCCAGGGATCCCCCACCCCACACTTTCTGTTCTGTCCCCACCATTGACCT... |
Task1_train_41408 | A variant on Chromosome 11 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | AGGATCCTCTAATGCGGGCGCAGGTGGCTCATGACCATCTCTGAGGGCTGGTTTCTCTTAATGCACCGGTTAGGAGCAATGGGCACCTTAAAGGGGCAGGCAGGCAGAGGTCGGGGGTCTGGGCCTTGCTGCTCCTGGCATCATGTCCTAAGACCCATGTTCTGAGTGTCCAGGTCCCTCCTCTGTCCCCGTTCATCCTTCCTCTGAGCTGTGCACCTGTCCCACCTGACAGTATGTCCCACTTGAAGGCAGCTCAGGGGTCCTGAGCCTTCCTACGGGGCTGCTGTGCTGGGACCTTCATACGCACACACACGCGCACA... | AGGATCCTCTAATGCGGGCGCAGGTGGCTCATGACCATCTCTGAGGGCTGGTTTCTCTTAATGCACCGGTTAGGAGCAATGGGCACCTTAAAGGGGCAGGCAGGCAGAGGTCGGGGGTCTGGGCCTTGCTGCTCCTGGCATCATGTCCTAAGACCCATGTTCTGAGTGTCCAGGTCCCTCCTCTGTCCCCGTTCATCCTTCCTCTGAGCTGTGCACCTGTCCCACCTGACAGTATGTCCCACTTGAAGGCAGCTCAGGGGTCCTGAGCCTTCCTACGGGGCTGCTGTGCTGGGACCTTCATACGCACACACACGCGCACA... |
Task1_train_41409 | A variant on Chromosome 11 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TTCTCTTAATGCACCGGTTAGGAGCAATGGGCACCTTAAAGGGGCAGGCAGGCAGAGGTCGGGGGTCTGGGCCTTGCTGCTCCTGGCATCATGTCCTAAGACCCATGTTCTGAGTGTCCAGGTCCCTCCTCTGTCCCCGTTCATCCTTCCTCTGAGCTGTGCACCTGTCCCACCTGACAGTATGTCCCACTTGAAGGCAGCTCAGGGGTCCTGAGCCTTCCTACGGGGCTGCTGTGCTGGGACCTTCATACGCACACACACGCGCACACGTGTTCACACATAATTACAGCCATACAAGCACAATCATACATATATACAAT... | TTCTCTTAATGCACCGGTTAGGAGCAATGGGCACCTTAAAGGGGCAGGCAGGCAGAGGTCGGGGGTCTGGGCCTTGCTGCTCCTGGCATCATGTCCTAAGACCCATGTTCTGAGTGTCCAGGTCCCTCCTCTGTCCCCGTTCATCCTTCCTCTGAGCTGTGCACCTGTCCCACCTGACAGTATGTCCCACTTGAAGGCAGCTCAGGGGTCCTGAGCCTTCCTACGGGGCTGCTGTGCTGGGACCTTCATACGCACACACACGCGCACACGTGTTCACACATAATTACAGCCATACAAGCACAATCATACATATATACAAT... |
Task1_train_41410 | This sequence change occurs on Chromosome 11. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GGCTGCCCTGGTCACTCTGTGGAACTTGATGGTGGTGAACAACTGGCAGGTGTTTCTGGATGCATATCGGCGCTACTCAGGCCCGTGAGTCCTCGTCTCCCTGACGGCAGTGATTCTCCGTGCAGCCTGGGGGTTCCCTCACCTCCGGGCACGCTGCATCTGCACTGGACGCCCGGAGCGTGGCTGGGACGGGGACTCGGGCCTTGACAGGGAAGTCGGCCAGCGTGGCATCCTGGCTTGCCTTGTCCCTGCCCCCTGCATAGCCACATCGTGACTCTCAGGATGGTGGCCAGTGACTCTGGGTTTACACCTCCTGGAGG... | GGCTGCCCTGGTCACTCTGTGGAACTTGATGGTGGTGAACAACTGGCAGGTGTTTCTGGATGCATATCGGCGCTACTCAGGCCCGTGAGTCCTCGTCTCCCTGACGGCAGTGATTCTCCGTGCAGCCTGGGGGTTCCCTCACCTCCGGGCACGCTGCATCTGCACTGGACGCCCGGAGCGTGGCTGGGACGGGGACTCGGGCCTTGACAGGGAAGTCGGCCAGCGTGGCATCCTGGCTTGCCTTGTCCCTGCCCCCTGCATAGCCACATCGTGACTCTCAGGATGGTGGCCAGTGACTCTGGGTTTACACCTCCTGGAGG... |
Task1_train_41411 | A mutation found on Chromosome 11 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GGAAATGTTGACGGGGAAGAAAGCCCTGCCCACCAGGCAGCCCCACCCACCTGGGCTAGCCCCACTCACAAGCAGCCCCACCCACCTGGGTTAGTCCCACCCACCAGGCAGCTCCGCCTACCTTGGCTATCCCCCTCTGAGTTCTTGCCTTGATTCTCCTGTTACTGTCCCGCGAACCCACATCCCTACAAAGCAGGAAAGTATGCTTGGGAGAGGCCAAGTGAGTGGGGAATCAGCCCAAAGCCAGGCGTCCAGGGTCTCCCTCACCTGAAGCTGACTTTTTCCCCACCTTGGACAGAGGGCGGGAGATGCCATCCCCA... | GGAAATGTTGACGGGGAAGAAAGCCCTGCCCACCAGGCAGCCCCACCCACCTGGGCTAGCCCCACTCACAAGCAGCCCCACCCACCTGGGTTAGTCCCACCCACCAGGCAGCTCCGCCTACCTTGGCTATCCCCCTCTGAGTTCTTGCCTTGATTCTCCTGTTACTGTCCCGCGAACCCACATCCCTACAAAGCAGGAAAGTATGCTTGGGAGAGGCCAAGTGAGTGGGGAATCAGCCCAAAGCCAGGCGTCCAGGGTCTCCCTCACCTGAAGCTGACTTTTTCCCCACCTTGGACAGAGGGCGGGAGATGCCATCCCCA... |
Task1_train_41412 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | TGCAGCCAGCTCACGTCCAGGTTCAACCCACAGCTACTTGGTTTGTGTTCTTCTTCATATTCTAAAACCATTCCATTTCCAAGCACTTTCAGTCCAATAGGTGTAGGAAATAGCGCTGTTTTTGTTGTGTGTGCAGGGAGGGCAGTTTTCTAATGGAATGGTTTGGGAATATCCATGTACTTGTTTGCAAGCAGGACTTTGAGGCAAGTGTGGGCCACTGTGGTGGCAGTGGAGGTGGGGTGTTTGGGAGGCTGCGTGCCAGTCAAGAAGAAAAAGGTTTGCATTCTCACATTGCCAGGATGATAAGTTCCTTTCCTTTT... | TGCAGCCAGCTCACGTCCAGGTTCAACCCACAGCTACTTGGTTTGTGTTCTTCTTCATATTCTAAAACCATTCCATTTCCAAGCACTTTCAGTCCAATAGGTGTAGGAAATAGCGCTGTTTTTGTTGTGTGTGCAGGGAGGGCAGTTTTCTAATGGAATGGTTTGGGAATATCCATGTACTTGTTTGCAAGCAGGACTTTGAGGCAAGTGTGGGCCACTGTGGTGGCAGTGGAGGTGGGGTGTTTGGGAGGCTGCGTGCCAGTCAAGAAGAAAAAGGTTTGCATTCTCACATTGCCAGGATGATAAGTTCCTTTCCTTTT... |
Task1_train_41413 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | GCCATGTATCACATTGGCTATCAGACCCTTCCAAGAAAAATGAGTTTTTATCTCGACTTCTGCACAATGGTCAGATGGAAAAGTTCTGTGAAATGAATGTAGCCCCTGCAAGGGTCCAGGAAGGCTCTGATTTCCATCCATCCTCTTTTGCCCTCCTGGGGCACACGTCCCGGGGCTTCTTGGCATGCTCTCCTGAGGGTGAGCCTGCCGCCCACGGAGAATAAAATCCCACTTGAGTGCCTGTGTGGGATTTTGAGTCCGGACTGAAACGAGATCATTTCTGAGTCCGGACTGAAACGAGATCATTGCTAAGGAAAATG... | GCCATGTATCACATTGGCTATCAGACCCTTCCAAGAAAAATGAGTTTTTATCTCGACTTCTGCACAATGGTCAGATGGAAAAGTTCTGTGAAATGAATGTAGCCCCTGCAAGGGTCCAGGAAGGCTCTGATTTCCATCCATCCTCTTTTGCCCTCCTGGGGCACACGTCCCGGGGCTTCTTGGCATGCTCTCCTGAGGGTGAGCCTGCCGCCCACGGAGAATAAAATCCCACTTGAGTGCCTGTGTGGGATTTTGAGTCCGGACTGAAACGAGATCATTTCTGAGTCCGGACTGAAACGAGATCATTGCTAAGGAAAATG... |
Task1_train_41414 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GGACAGCCTCCACTCGAGGCCTTCCCTCCCCCTCTCCCCCACTGCAGTGCTGACTGTTTGGGGAGGGGCTCCACCCTCCGGCTTCCCTGATACACTTTGGGTTGTATACAGCCCACCTGCCTCGAATGAGGGATTCTGCCTGCCCCTTTTCCCGACCAGTGCACAGCCATTTAGAGCCATGGTGCAGCCGGAAGCTGCCCAGGGGCTCCAGGCGACCACGTGGGGGGACCCTCCAGGCCAGCGAGGCCCAAGCACAGCTCTGTCCAAAGGCCACAGGTGCTCGGGCCCTGCCTGGCGCAGCATGCCGTCCCTGCACTCCA... | GGACAGCCTCCACTCGAGGCCTTCCCTCCCCCTCTCCCCCACTGCAGTGCTGACTGTTTGGGGAGGGGCTCCACCCTCCGGCTTCCCTGATACACTTTGGGTTGTATACAGCCCACCTGCCTCGAATGAGGGATTCTGCCTGCCCCTTTTCCCGACCAGTGCACAGCCATTTAGAGCCATGGTGCAGCCGGAAGCTGCCCAGGGGCTCCAGGCGACCACGTGGGGGGACCCTCCAGGCCAGCGAGGCCCAAGCACAGCTCTGTCCAAAGGCCACAGGTGCTCGGGCCCTGCCTGGCGCAGCATGCCGTCCCTGCACTCCA... |
Task1_train_41415 | A genomic variant on Chromosome 11 is under review. What is the biological outcome — benign or pathogenic? | Benign | GAAGGGTTCTGACTCGCTGGTGGGTTTAATCCAGTAGAAGTGTCTTTATTGAAAGAGACAGGGGCCAGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGACCGAGGCAGGTGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATATCAAAAATTAGCCGGGTGTGGTGGTGCACACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAAGAGAATCACTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATCGTGCCACTACACTCCAGCTT... | GAAGGGTTCTGACTCGCTGGTGGGTTTAATCCAGTAGAAGTGTCTTTATTGAAAGAGACAGGGGCCAGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGACCGAGGCAGGTGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATATCAAAAATTAGCCGGGTGTGGTGGTGCACACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAAGAGAATCACTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATCGTGCCACTACACTCCAGCTT... |
Task1_train_41416 | A variant on Chromosome 11 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | CCTGACGTGCCGGACGCGTCCAGCTCAGAACTCGAGGCGCGGTAGACACTCAGCAAAGGCCTCCGGCGTCCCTGCAGCCGTGGGGGGAAACTGGGGACGCCCGGAGGAAGACGCTGACCCGGCGAGCACCTGAGCGCCCACCTGTGGCTCATCCCGGAGACCGCCCCCTCCCCCGCGACCCGGGCGGGGCCTGGGGGGCGTGGCTCCCGTCTCGCTCAGCCAATCAGTGCCCCGGGGCCGCCTCCCGCCCCCTCCTGAGGAGACAGCGCTTGCGTACTCGGGCCAAGGTGCTCCTCGGGCCCCGCCCCCGGGGCGGTGCT... | CCTGACGTGCCGGACGCGTCCAGCTCAGAACTCGAGGCGCGGTAGACACTCAGCAAAGGCCTCCGGCGTCCCTGCAGCCGTGGGGGGAAACTGGGGACGCCCGGAGGAAGACGCTGACCCGGCGAGCACCTGAGCGCCCACCTGTGGCTCATCCCGGAGACCGCCCCCTCCCCCGCGACCCGGGCGGGGCCTGGGGGGCGTGGCTCCCGTCTCGCTCAGCCAATCAGTGCCCCGGGGCCGCCTCCCGCCCCCTCCTGAGGAGACAGCGCTTGCGTACTCGGGCCAAGGTGCTCCTCGGGCCCCGCCCCCGGGGCGGTGCT... |
Task1_train_41417 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GCGTGTGCCCCTCTCCTCTTTGTCACTGCTTCCCTTGCCCTGGATGTGGTTGGTGCACTGGGGTCACCTTAGACCACAGGAAATGTCTGGTTAACACACGAAGAGATGGAAACGCTCGCAGCCACGCCGCAAACGGTTAGTCACGCCCCACAGCCTGCACTCCTCCCAGCGCGTTTTCCACTTAAGACCGTCTGGGTTCTTTGCCTTTTTGTTGAAAACAAAATGTTGTTTTCCATTCAGTCGTTCCAGATAAGTATTTCCTTTAGTTATTAGTTGAAATGTGTAAGTAGAATTTGTATTTTATTTTAGATTTTTTCCAG... | GCGTGTGCCCCTCTCCTCTTTGTCACTGCTTCCCTTGCCCTGGATGTGGTTGGTGCACTGGGGTCACCTTAGACCACAGGAAATGTCTGGTTAACACACGAAGAGATGGAAACGCTCGCAGCCACGCCGCAAACGGTTAGTCACGCCCCACAGCCTGCACTCCTCCCAGCGCGTTTTCCACTTAAGACCGTCTGGGTTCTTTGCCTTTTTGTTGAAAACAAAATGTTGTTTTCCATTCAGTCGTTCCAGATAAGTATTTCCTTTAGTTATTAGTTGAAATGTGTAAGTAGAATTTGTATTTTATTTTAGATTTTTTCCAG... |
Task1_train_41418 | A variant on Chromosome 11 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GCTCTCTGCTGTGCAGGACGCCGCCTCACTCCCTAATGGCAGTGCTGCCCTCCTTCATCACTGAGCCCCTGCCTCCCGCACAATCTGCCTTCTATGCCTGCCCCATTCAGCTCTCCAGCCTTGCAGCCCCTCATGAGTGTGGCTGCAGACATGCTGTCCGGCCCCTCCCTGTGCTGCTGACCCCCTCTCATGGGTCCCCCAGTGTTCCGTCCCCATCCCTGAGTTACGGAGCCGCCTGCCGATGCCCCGCCCATCCCTGACTTTGGGTCTCCTGCTCCCCGCCAGCACCTCTGCGCTAACCACACCCTCTACCTGTAACC... | GCTCTCTGCTGTGCAGGACGCCGCCTCACTCCCTAATGGCAGTGCTGCCCTCCTTCATCACTGAGCCCCTGCCTCCCGCACAATCTGCCTTCTATGCCTGCCCCATTCAGCTCTCCAGCCTTGCAGCCCCTCATGAGTGTGGCTGCAGACATGCTGTCCGGCCCCTCCCTGTGCTGCTGACCCCCTCTCATGGGTCCCCCAGTGTTCCGTCCCCATCCCTGAGTTACGGAGCCGCCTGCCGATGCCCCGCCCATCCCTGACTTTGGGTCTCCTGCTCCCCGCCAGCACCTCTGCGCTAACCACACCCTCTACCTGTAACC... |
Task1_train_41419 | A genomic variant on Chromosome 11 is under review. What is the biological outcome — benign or pathogenic? | Benign | AAGCTGAGACACTGAGAGGGTAGGTCCCCTGAAGGTCATACAGCTCTTAAATGCTGGGGCCAGGATTCCAACGCAGGCAGGGAGGCCCGGATCTGAGCTCACAGTGACCACACCCCAGCCTCTGTGAACTGAATTTACGCAATGTCTGGGAAGAAAAGGCAGGGTCCACTCCGCTCAGAGCCATGCAGGGCAGTGTGCTCCCGTCTCCCCGGCATTTGAATCACTCTTGTGGTGTGTGTCCAGCACAGATGCACGGGACCCCTCAGGCCCATATCCTCAAACAGGTAGTGGTGGGGCACCAGTGCACGAACACTAGGGCT... | AAGCTGAGACACTGAGAGGGTAGGTCCCCTGAAGGTCATACAGCTCTTAAATGCTGGGGCCAGGATTCCAACGCAGGCAGGGAGGCCCGGATCTGAGCTCACAGTGACCACACCCCAGCCTCTGTGAACTGAATTTACGCAATGTCTGGGAAGAAAAGGCAGGGTCCACTCCGCTCAGAGCCATGCAGGGCAGTGTGCTCCCGTCTCCCCGGCATTTGAATCACTCTTGTGGTGTGTGTCCAGCACAGATGCACGGGACCCCTCAGGCCCATATCCTCAAACAGGTAGTGGTGGGGCACCAGTGCACGAACACTAGGGCT... |
Task1_train_41420 | This genomic variant is located on Chromosome 11. Can you determine its pathogenicity and name any linked disease? | Benign | CCTGATCGTCTCGTGAGCCTGACCTCTCCTGGGCTGGTCCGGGGGCCTGATCCTCATGTCCTGTCTGCTGCTTGCCCTGGAGGAGCTGCAGTGGTGACAGCCCAGTCCCCCTGGCCTGATGTTGCCCAGATGCTTAGAGTTTACGTCTTCTTTTCTTTCTTCGTCCTAGTCTCTCTCTCCTATAAATGTTACATCCACCTCTCTCTTTCCTCCAAATATGGACCTGTTTCATTTTAAAAGTGGGAGGATGTCTAACTAAAGGCCCCCGGGATGGAATATTTGCATCCAGCAGGGACAGGGGCCCAGCTGAGCAGGTCTCC... | CCTGATCGTCTCGTGAGCCTGACCTCTCCTGGGCTGGTCCGGGGGCCTGATCCTCATGTCCTGTCTGCTGCTTGCCCTGGAGGAGCTGCAGTGGTGACAGCCCAGTCCCCCTGGCCTGATGTTGCCCAGATGCTTAGAGTTTACGTCTTCTTTTCTTTCTTCGTCCTAGTCTCTCTCTCCTATAAATGTTACATCCACCTCTCTCTTTCCTCCAAATATGGACCTGTTTCATTTTAAAAGTGGGAGGATGTCTAACTAAAGGCCCCCGGGATGGAATATTTGCATCCAGCAGGGACAGGGGCCCAGCTGAGCAGGTCTCC... |
Task1_train_41421 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AGACAGTCAGCGTGCTAGGGGCTGCCACACAAGGAAGACCCAAGCAGCCTTGGAGCCCAGGAAGGCCTCAAGGTGAGGGGTGGCAAGCGTGGTAGGAACAGGCACACAGTGTGCAGCCGAGGCTGGTCCCCACTTCGGCAGTTGGAGGCAAGGTCCAAGGCACAAGTGAGCCTGTGTCTGAGACCCTGGGATGCAAGTAACGCCCCTCCTGCAGCCCGAGGTCCTGCTGCTGGTAACCTGGAGCTCTGCGTTTCTGCAGGACATCGTCACAAATAGGATGTCCAACTGAGCAGCTGTCATGAGACAGTGATTTTTGCAAA... | AGACAGTCAGCGTGCTAGGGGCTGCCACACAAGGAAGACCCAAGCAGCCTTGGAGCCCAGGAAGGCCTCAAGGTGAGGGGTGGCAAGCGTGGTAGGAACAGGCACACAGTGTGCAGCCGAGGCTGGTCCCCACTTCGGCAGTTGGAGGCAAGGTCCAAGGCACAAGTGAGCCTGTGTCTGAGACCCTGGGATGCAAGTAACGCCCCTCCTGCAGCCCGAGGTCCTGCTGCTGGTAACCTGGAGCTCTGCGTTTCTGCAGGACATCGTCACAAATAGGATGTCCAACTGAGCAGCTGTCATGAGACAGTGATTTTTGCAAA... |
Task1_train_41422 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | GAGAGGAATCCAAGCAGGCTATAGAGCAACCACCTGCTAGAGATATTAGCATGACTCAAAAAACAAACAAAAAAACCCAAGTGCTAATAGCCAACACAATTGGAAAAGACTTCAAATGCATTTCAAAAGTGTTTGAGACAGCCCCTCTCATCACTGACCTAGAGGTCTAGGAGGACACCATGGTTTCAGGGGCTCACCCCAGGCCCTCACTGCCCTGCATAGCCTTGGAGCACTGCTCCCCACACATAGGCTACTCCAGCTCCAGCCTCAGCTCAAAAGACCCCAAATGTAACTCTGGCTTCAGAGGGTGCAAGCCATAA... | GAGAGGAATCCAAGCAGGCTATAGAGCAACCACCTGCTAGAGATATTAGCATGACTCAAAAAACAAACAAAAAAACCCAAGTGCTAATAGCCAACACAATTGGAAAAGACTTCAAATGCATTTCAAAAGTGTTTGAGACAGCCCCTCTCATCACTGACCTAGAGGTCTAGGAGGACACCATGGTTTCAGGGGCTCACCCCAGGCCCTCACTGCCCTGCATAGCCTTGGAGCACTGCTCCCCACACATAGGCTACTCCAGCTCCAGCCTCAGCTCAAAAGACCCCAAATGTAACTCTGGCTTCAGAGGGTGCAAGCCATAA... |
Task1_train_41423 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CAAGGATGAGAGCAGAGCCAGCTTGGCATCGTGGGAATCAATAAATGAAACAGAAAGTGCAAGGTGGTGGGGGTAGCTATCTCGGGACGGGGTGTCAGAGGTGGATCTGAGTTGGGCAGACAGGAGGGACGCAGTCCAGGGCGGTCCTGGGTGAGTCTGTTCCATGTAAGGAACTGCCAGCACACAGGTCGTAAGGAGGAGTGCGGTGTGGCCCCGGCACCAATCCAGGGCTGGATGAAGAATGATTGAGGCAGTCTGAAGATGACACCAAGTCATTCTCCTCCCACGGAGAGGTGGACTTTCTCTTCTCTCTGCAATCT... | CAAGGATGAGAGCAGAGCCAGCTTGGCATCGTGGGAATCAATAAATGAAACAGAAAGTGCAAGGTGGTGGGGGTAGCTATCTCGGGACGGGGTGTCAGAGGTGGATCTGAGTTGGGCAGACAGGAGGGACGCAGTCCAGGGCGGTCCTGGGTGAGTCTGTTCCATGTAAGGAACTGCCAGCACACAGGTCGTAAGGAGGAGTGCGGTGTGGCCCCGGCACCAATCCAGGGCTGGATGAAGAATGATTGAGGCAGTCTGAAGATGACACCAAGTCATTCTCCTCCCACGGAGAGGTGGACTTTCTCTTCTCTCTGCAATCT... |
Task1_train_41424 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | GCAGTCACGCCTGAGAACCACAAGTGAGACACGGGGAGAATTGCATTGGTCTGAAGCCGCCTGGAGAACCGTCCTGTGGGGTAGTGAGTGGGGGGTACTAAAGGGCATGAGGTTATGAAATTTTCTACAACTGATTATGGTGATAGGTACACGGCTCTGTGAATATACTAAAAGCATTGAATTGTATACCTTAAATGGGAGAATTGTGTGGTATATGAACGATATGTCAATAAAGCTGTTAACAAAACAAGAAGAGGTATCAGAGAGGTTGGGGATCAGTGAAGCCGTGGTTGTATCAATGCACCAAGAGTTCTGGTGGA... | GCAGTCACGCCTGAGAACCACAAGTGAGACACGGGGAGAATTGCATTGGTCTGAAGCCGCCTGGAGAACCGTCCTGTGGGGTAGTGAGTGGGGGGTACTAAAGGGCATGAGGTTATGAAATTTTCTACAACTGATTATGGTGATAGGTACACGGCTCTGTGAATATACTAAAAGCATTGAATTGTATACCTTAAATGGGAGAATTGTGTGGTATATGAACGATATGTCAATAAAGCTGTTAACAAAACAAGAAGAGGTATCAGAGAGGTTGGGGATCAGTGAAGCCGTGGTTGTATCAATGCACCAAGAGTTCTGGTGGA... |
Task1_train_41425 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TGGGCCTTCCCTCCTCTTCCATAGAGCCAGACAGTTGGCGACTGTCTTTACTGCAAACGCTGGTTCACACTGGCTCCCCTGGGAGGGAGGTGGTTTGGGCCCACGTGCCCTGTGTTCCTGCTCAGAATGGGCATTAGAAATGCTGCCATAGCCTGTGCCACTGCAGTGGAAGCATTTTTAGGAAACGGCTTATAGCTTAAGACAAACTTCAGATGCATGGGGCCAGAACGCTGTGTCCATCTGCATCTTTGCTGAGGGATCCGGTAGCCTGGAGTTTGCCCTCTGCCATGTTGGCTTGAGGCTCATAGGCGACTTAAGAC... | TGGGCCTTCCCTCCTCTTCCATAGAGCCAGACAGTTGGCGACTGTCTTTACTGCAAACGCTGGTTCACACTGGCTCCCCTGGGAGGGAGGTGGTTTGGGCCCACGTGCCCTGTGTTCCTGCTCAGAATGGGCATTAGAAATGCTGCCATAGCCTGTGCCACTGCAGTGGAAGCATTTTTAGGAAACGGCTTATAGCTTAAGACAAACTTCAGATGCATGGGGCCAGAACGCTGTGTCCATCTGCATCTTTGCTGAGGGATCCGGTAGCCTGGAGTTTGCCCTCTGCCATGTTGGCTTGAGGCTCATAGGCGACTTAAGAC... |
Task1_train_41426 | A mutation is present on Chromosome 11. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GGTTGTAGTGAGCCAAGATCGCGCTATTGCACTCCCACCTGGGCAACGAGAGTGAAACTGTCAAAAAGAAGTAGAAAAATTAGCCAGACATGGTGACACATGCCTGTAGTCGCACCTACTTGGGCAGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCAAGATTGTGCCACTGACTCCAGCCTGGGGAACAGAGCTCAAAAAAAATAAGATAAAACATAGATACAGAAAACCACAAAGGAAAAACATAGCATATTGAATCATCACAAGGCAGCCACCCCTTCATAGCCACACCCGGCCCCT... | GGTTGTAGTGAGCCAAGATCGCGCTATTGCACTCCCACCTGGGCAACGAGAGTGAAACTGTCAAAAAGAAGTAGAAAAATTAGCCAGACATGGTGACACATGCCTGTAGTCGCACCTACTTGGGCAGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCAAGATTGTGCCACTGACTCCAGCCTGGGGAACAGAGCTCAAAAAAAATAAGATAAAACATAGATACAGAAAACCACAAAGGAAAAACATAGCATATTGAATCATCACAAGGCAGCCACCCCTTCATAGCCACACCCGGCCCCT... |
Task1_train_41427 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TTCTCTTGAGTTTTAGGTTCAGTGGTGAGGCTCCTTCACGGACAATACATTTTCCAATTCTGAGGACAAGGCAGAGGAGGGCCCCTCTGTGAGAACTTTCATTTTGCTTCGGGAAAAGTACATTGAATCAAATATAGGAAAGACTTGCAAGGTAGCTGACAGGTTCGGCTGTTTTATCATGCTGGTGTTTTATCTTCTGGACTGCAGTAAAAGGAGCACAGCTGTGTCTATCTCTGTGTAATAACTCAGGACTTACCTGAATAAAATGTGGGGTGTTATGAGATGAACTTCTACTTCCAGTTAGAGAGGCTCCAGGGACA... | TTCTCTTGAGTTTTAGGTTCAGTGGTGAGGCTCCTTCACGGACAATACATTTTCCAATTCTGAGGACAAGGCAGAGGAGGGCCCCTCTGTGAGAACTTTCATTTTGCTTCGGGAAAAGTACATTGAATCAAATATAGGAAAGACTTGCAAGGTAGCTGACAGGTTCGGCTGTTTTATCATGCTGGTGTTTTATCTTCTGGACTGCAGTAAAAGGAGCACAGCTGTGTCTATCTCTGTGTAATAACTCAGGACTTACCTGAATAAAATGTGGGGTGTTATGAGATGAACTTCTACTTCCAGTTAGAGAGGCTCCAGGGACA... |
Task1_train_41428 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | GACTGCAGTAAAAGGAGCACAGCTGTGTCTATCTCTGTGTAATAACTCAGGACTTACCTGAATAAAATGTGGGGTGTTATGAGATGAACTTCTACTTCCAGTTAGAGAGGCTCCAGGGACAAAATTTCAAGAGCCTTCTGAGGGATAGAAGAGAAGAGCTCCCTTATTCTCTGATCCCAGGTAACTGCTCAGAGACAGAGGAAAGGGCTGGGGACACCCAAATGCATATACTAAGTGTCTTTGATACAGCCTCCATTTCCCTGCTAAATCTATGCAATGACACACTGAGAAATCTAGCAAGTGGGGCTGAAGATCCCTGG... | GACTGCAGTAAAAGGAGCACAGCTGTGTCTATCTCTGTGTAATAACTCAGGACTTACCTGAATAAAATGTGGGGTGTTATGAGATGAACTTCTACTTCCAGTTAGAGAGGCTCCAGGGACAAAATTTCAAGAGCCTTCTGAGGGATAGAAGAGAAGAGCTCCCTTATTCTCTGATCCCAGGTAACTGCTCAGAGACAGAGGAAAGGGCTGGGGACACCCAAATGCATATACTAAGTGTCTTTGATACAGCCTCCATTTCCCTGCTAAATCTATGCAATGACACACTGAGAAATCTAGCAAGTGGGGCTGAAGATCCCTGG... |
Task1_train_41429 | A mutation is present on Chromosome 11. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | AACAAGTCTTTGGTACATACATGTCATACAATTTCTCTTCCATATGAATTTATTGATGTGGACTGAAGAATAAAGGTAACTGAAGTATCTTCCATGTTGATTACAGTATTTCTTCAAAATGTTAGTCCTTTGGCATGTTCAGATGCTACAACTACAGCTGAAGTCTCTTCCACATTCCTTACCTTCGTCATTCCTAACACCGTGTCATCTAAAGTCAGAATATGTTCTGAAGATGTTTATAATTTTCTCTCCAGCGTGAATTTTCTGATGTTATTTAAGATTAGTACATTGACTGAAGGCTTTCCCACATAAATGGCATT... | AACAAGTCTTTGGTACATACATGTCATACAATTTCTCTTCCATATGAATTTATTGATGTGGACTGAAGAATAAAGGTAACTGAAGTATCTTCCATGTTGATTACAGTATTTCTTCAAAATGTTAGTCCTTTGGCATGTTCAGATGCTACAACTACAGCTGAAGTCTCTTCCACATTCCTTACCTTCGTCATTCCTAACACCGTGTCATCTAAAGTCAGAATATGTTCTGAAGATGTTTATAATTTTCTCTCCAGCGTGAATTTTCTGATGTTATTTAAGATTAGTACATTGACTGAAGGCTTTCCCACATAAATGGCATT... |
Task1_train_41430 | This is a variant located on Chromosome 11. Is this mutation a likely cause of disease or not? | Benign | GAATAAAGTCCTCCAGCTGCATCCATGTTACTGAAAAAGACACAGTTTTGTTCTTTTTATGGCTGCATAGTATTCCATGACATATATGTACTACATTTGCTTTATTCAATCCACTGTTGATGAACACCTAGTTTGATTCCATACCTTTGCTACTGTGAATACCACTGTGATGAACATACAAATTTAGGTCTTTTTACAAGACTGATTTATTTTCCTTTGGATATACACCCAGTAGTGAGATTACTGGGTCAAATGGTAGTTCTGTATTAAGTTTCTTGAAAAGTGGTTTGAAAATATAATGCTCAATAGAATCAGGTATA... | GAATAAAGTCCTCCAGCTGCATCCATGTTACTGAAAAAGACACAGTTTTGTTCTTTTTATGGCTGCATAGTATTCCATGACATATATGTACTACATTTGCTTTATTCAATCCACTGTTGATGAACACCTAGTTTGATTCCATACCTTTGCTACTGTGAATACCACTGTGATGAACATACAAATTTAGGTCTTTTTACAAGACTGATTTATTTTCCTTTGGATATACACCCAGTAGTGAGATTACTGGGTCAAATGGTAGTTCTGTATTAAGTTTCTTGAAAAGTGGTTTGAAAATATAATGCTCAATAGAATCAGGTATA... |
Task1_train_41431 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TTTATGGCTGCATAGTATTCCATGACATATATGTACTACATTTGCTTTATTCAATCCACTGTTGATGAACACCTAGTTTGATTCCATACCTTTGCTACTGTGAATACCACTGTGATGAACATACAAATTTAGGTCTTTTTACAAGACTGATTTATTTTCCTTTGGATATACACCCAGTAGTGAGATTACTGGGTCAAATGGTAGTTCTGTATTAAGTTTCTTGAAAAGTGGTTTGAAAATATAATGCTCAATAGAATCAGGTATAGTAACATAGTACACATGATTCAAAGACCTGTGAACCGAGAGTAACAACAAATTTC... | TTTATGGCTGCATAGTATTCCATGACATATATGTACTACATTTGCTTTATTCAATCCACTGTTGATGAACACCTAGTTTGATTCCATACCTTTGCTACTGTGAATACCACTGTGATGAACATACAAATTTAGGTCTTTTTACAAGACTGATTTATTTTCCTTTGGATATACACCCAGTAGTGAGATTACTGGGTCAAATGGTAGTTCTGTATTAAGTTTCTTGAAAAGTGGTTTGAAAATATAATGCTCAATAGAATCAGGTATAGTAACATAGTACACATGATTCAAAGACCTGTGAACCGAGAGTAACAACAAATTTC... |
Task1_train_41432 | This sequence change occurs on Chromosome 11. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | ACATATATGTACTACATTTGCTTTATTCAATCCACTGTTGATGAACACCTAGTTTGATTCCATACCTTTGCTACTGTGAATACCACTGTGATGAACATACAAATTTAGGTCTTTTTACAAGACTGATTTATTTTCCTTTGGATATACACCCAGTAGTGAGATTACTGGGTCAAATGGTAGTTCTGTATTAAGTTTCTTGAAAAGTGGTTTGAAAATATAATGCTCAATAGAATCAGGTATAGTAACATAGTACACATGATTCAAAGACCTGTGAACCGAGAGTAACAACAAATTTCTGCACAAACATATTGCAAGTTAGA... | ACATATATGTACTACATTTGCTTTATTCAATCCACTGTTGATGAACACCTAGTTTGATTCCATACCTTTGCTACTGTGAATACCACTGTGATGAACATACAAATTTAGGTCTTTTTACAAGACTGATTTATTTTCCTTTGGATATACACCCAGTAGTGAGATTACTGGGTCAAATGGTAGTTCTGTATTAAGTTTCTTGAAAAGTGGTTTGAAAATATAATGCTCAATAGAATCAGGTATAGTAACATAGTACACATGATTCAAAGACCTGTGAACCGAGAGTAACAACAAATTTCTGCACAAACATATTGCAAGTTAGA... |
Task1_train_41433 | A genomic variant on Chromosome 11 is under review. What is the biological outcome — benign or pathogenic? | Benign | GCGAGCCGGACAGGCGGCTGCCTGCACACCCCGAGGCGGGGACTGTGTAGAAATCTGGGGCTTTAACAGGGGTAGGAGCCCGGCTTGGCGTCTCCTCTGTAATCTGTCCCCTCCAGGCCTCCGTATTCAGTGAGCCCTGCAGTCCGGCTGCCCGTCCTCCGCAGGTTTCTTTCTGGGCCCCATGCCCCAGTGTCTTAGCCCTCATTCCCGAGCCCCGCCTGCCGCGGCCGCACCTGGTCCGAGTCCTCGTTCTCGCTGCTGTAGCAGCACCCCATGGCCGGGGTCGGGCCGGGCGCTCAGGCCGCGCCGAGGAGGGACGG... | GCGAGCCGGACAGGCGGCTGCCTGCACACCCCGAGGCGGGGACTGTGTAGAAATCTGGGGCTTTAACAGGGGTAGGAGCCCGGCTTGGCGTCTCCTCTGTAATCTGTCCCCTCCAGGCCTCCGTATTCAGTGAGCCCTGCAGTCCGGCTGCCCGTCCTCCGCAGGTTTCTTTCTGGGCCCCATGCCCCAGTGTCTTAGCCCTCATTCCCGAGCCCCGCCTGCCGCGGCCGCACCTGGTCCGAGTCCTCGTTCTCGCTGCTGTAGCAGCACCCCATGGCCGGGGTCGGGCCGGGCGCTCAGGCCGCGCCGAGGAGGGACGG... |
Task1_train_41434 | Here is a genetic alteration on Chromosome 11. Based on the data, is it a benign variant or a cause of disease? | Benign | GGAACAAGGGGGCTGTGGGCGTCTCCTTCATGTTTAATGGCACCTCATTTGGCTTTGTGAATTGTCACCTCACCTCGGGAAATGAGAAGACGGCTCGGTGAGGGGGCGCCTTTCCCATGGTCTCTTTACACCCATCCCATTCACCTGAGGCCTGTTCCCGCTCCCATACCCTAGCCCATGACCCTCCCGCAGGCCTGTCTCCAGAGACCCCCTGCTCTCTTATCCCAATTCAAGACCCTTCTGTTCCTGACCCTAACCTTGTCCCCAGGGGCCCGGATCTTTACCCCATCCCTGACTCCTGAGACTTCTTCCCTTTATGC... | GGAACAAGGGGGCTGTGGGCGTCTCCTTCATGTTTAATGGCACCTCATTTGGCTTTGTGAATTGTCACCTCACCTCGGGAAATGAGAAGACGGCTCGGTGAGGGGGCGCCTTTCCCATGGTCTCTTTACACCCATCCCATTCACCTGAGGCCTGTTCCCGCTCCCATACCCTAGCCCATGACCCTCCCGCAGGCCTGTCTCCAGAGACCCCCTGCTCTCTTATCCCAATTCAAGACCCTTCTGTTCCTGACCCTAACCTTGTCCCCAGGGGCCCGGATCTTTACCCCATCCCTGACTCCTGAGACTTCTTCCCTTTATGC... |
Task1_train_41435 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | AAGCCCAGCGTCACCCACCTGCCTCCTCCCTCTCGTTGACCTCAAAGCAGGTCCAATAGTCCTTCTCCCTGATGCCCACGTTCCGGCGATCCAGGATCTCCAGGGTGAGCTCCTCAGCAGTCATGGATGCTGGGACCTGCAAGGACCAAGGAGGAGATTAGCCTGCCTGTGCCTAGCCCCTGCTCTGCCACAACCTTGCTATGTGACTCAGAGCCTGAGCCCATCCTTCTCAGGCCCTTCTGGAGTCCTGGGATAGAGAGGGGTATTTCTGAGTGGTCCTTAGGAGCAGACCCCAGCACCAGCCAGATACAGGTCCCAAA... | AAGCCCAGCGTCACCCACCTGCCTCCTCCCTCTCGTTGACCTCAAAGCAGGTCCAATAGTCCTTCTCCCTGATGCCCACGTTCCGGCGATCCAGGATCTCCAGGGTGAGCTCCTCAGCAGTCATGGATGCTGGGACCTGCAAGGACCAAGGAGGAGATTAGCCTGCCTGTGCCTAGCCCCTGCTCTGCCACAACCTTGCTATGTGACTCAGAGCCTGAGCCCATCCTTCTCAGGCCCTTCTGGAGTCCTGGGATAGAGAGGGGTATTTCTGAGTGGTCCTTAGGAGCAGACCCCAGCACCAGCCAGATACAGGTCCCAAA... |
Task1_train_41436 | A mutation has occurred on Chromosome 11. What is the medical relevance of this mutation? | Benign | AACTTCCGGGCCCCAAGTTCATATGGGGTCAAAAACACTGCAGAGGAGCAGAGCATAGGCCCCTCCTCTGGTCCTGGCAGCAGGGGTGTCCCTTGGGCAGCAGAGGGCACCTGGGGGCCACAGATCACAGGGGAGGCCCAGGCGTCCCTCTAGACTTCAGACCAGCGAGGTGCAGCACAGGGTGAGAAGGCTGGCATCTGACCACTGGCAAGGGGATAGGGGGTCTGGGGACCCTACCATTTCTGTTAACACAGTCCTGAGGTCTTCAAAATGACCTAGGGAGGGCGTGAATCACCAAGCCTGGTCCCCACCAACTGCAC... | AACTTCCGGGCCCCAAGTTCATATGGGGTCAAAAACACTGCAGAGGAGCAGAGCATAGGCCCCTCCTCTGGTCCTGGCAGCAGGGGTGTCCCTTGGGCAGCAGAGGGCACCTGGGGGCCACAGATCACAGGGGAGGCCCAGGCGTCCCTCTAGACTTCAGACCAGCGAGGTGCAGCACAGGGTGAGAAGGCTGGCATCTGACCACTGGCAAGGGGATAGGGGGTCTGGGGACCCTACCATTTCTGTTAACACAGTCCTGAGGTCTTCAAAATGACCTAGGGAGGGCGTGAATCACCAAGCCTGGTCCCCACCAACTGCAC... |
Task1_train_41437 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | CAAGGTTGGGGGGGACACCATGATACTGACGATATGCAGAGAGAAACTGGATAGGCATGGAAGAAGCTGCATTTACCACACAAAAGAAGATCCCTTGGCCCCCTATCCCTATCTCCAACCCAGATTTCCCTGGACTCTTCACGGGGGTTACTTCAGGGGGATTCCCTGGTAGCCTCACAGGCTCAGGGGCAGGACTGCTGTTGATAGATATAGAAAGTGCCAGAATAGAGGAAGATGTAAAAAGTGAAGGAATAACTGAAGAAGGAGACCCTTGGAAATACTTCCTCAAATACCAGAACACTAGGCATGGGCCCAGAGCC... | CAAGGTTGGGGGGGACACCATGATACTGACGATATGCAGAGAGAAACTGGATAGGCATGGAAGAAGCTGCATTTACCACACAAAAGAAGATCCCTTGGCCCCCTATCCCTATCTCCAACCCAGATTTCCCTGGACTCTTCACGGGGGTTACTTCAGGGGGATTCCCTGGTAGCCTCACAGGCTCAGGGGCAGGACTGCTGTTGATAGATATAGAAAGTGCCAGAATAGAGGAAGATGTAAAAAGTGAAGGAATAACTGAAGAAGGAGACCCTTGGAAATACTTCCTCAAATACCAGAACACTAGGCATGGGCCCAGAGCC... |
Task1_train_41438 | Assess the clinical impact of this variant found on Chromosome 11. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GGTGGAAGGCGTGGCAGCTGGAAAAGTAGGGGTGGGGGCGCGGTCGTGAAGGGTGGGACTTCTGGAGCAACGCTGGGCGGGTTGGGGGCCGGTCGGAGCCGGACAGGCGGCTGGGAGGTGGGATGGGCGGGGCGCTTGGGAGCGAGATGGGGGGACAAGGGCGTGGCTACAGCTAAATTCGCCGCAGAGGGCGGGCGGGGAGGGGGAGGGAAGGGGAGGAGGCGTGGCCTGGGCGGGGAGTAGGGCGCGACGGACCCTTCAGTTAGCCCGCGGCTCCCCGGGCTCTCCCTGGCGCCGAGTCCCACCCCTTTCCCGGCCCA... | GGTGGAAGGCGTGGCAGCTGGAAAAGTAGGGGTGGGGGCGCGGTCGTGAAGGGTGGGACTTCTGGAGCAACGCTGGGCGGGTTGGGGGCCGGTCGGAGCCGGACAGGCGGCTGGGAGGTGGGATGGGCGGGGCGCTTGGGAGCGAGATGGGGGGACAAGGGCGTGGCTACAGCTAAATTCGCCGCAGAGGGCGGGCGGGGAGGGGGAGGGAAGGGGAGGAGGCGTGGCCTGGGCGGGGAGTAGGGCGCGACGGACCCTTCAGTTAGCCCGCGGCTCCCCGGGCTCTCCCTGGCGCCGAGTCCCACCCCTTTCCCGGCCCA... |
Task1_train_41439 | A variant found on Chromosome 11 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GGGAGAGGGAGAGGAATAGCTGAACTCTTGAATCCTCCTGGTGCATCTTAGAACATTATCTTTTGTGTAAGTGGGTTCCTAAGAATTAGGAGAGGTATCTTAATTTTCTTTTTATTTTTTATATTTACTTTAAAATTTTTTGTAGAGATGGAGTCTCATTATATTGCCCAGGCTGGTCTCGAACTCCTGGGCTCAAGTAATCTTCCTGCCTTGGCCTCCCAGAGTGTTGGGATTACACAGGTGTGAGCCACTGCACCTGGTCTTAATTTTAAAATAAAATAGCAGGGCTGGGCACGGTGGCCTATAATCCCAGCACTCTG... | GGGAGAGGGAGAGGAATAGCTGAACTCTTGAATCCTCCTGGTGCATCTTAGAACATTATCTTTTGTGTAAGTGGGTTCCTAAGAATTAGGAGAGGTATCTTAATTTTCTTTTTATTTTTTATATTTACTTTAAAATTTTTTGTAGAGATGGAGTCTCATTATATTGCCCAGGCTGGTCTCGAACTCCTGGGCTCAAGTAATCTTCCTGCCTTGGCCTCCCAGAGTGTTGGGATTACACAGGTGTGAGCCACTGCACCTGGTCTTAATTTTAAAATAAAATAGCAGGGCTGGGCACGGTGGCCTATAATCCCAGCACTCTG... |
Task1_train_41440 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GGTGAAAGTAGGACACAGTTGCACCACCTGACTTGCATCACCTCATTGCCTTCTAGTGGCGTTATAAGCTTGGTTCCCTGCTGACTGACACCTGGGAAGGGGTGGTGGGCACCTCAGGGCACCTCTTTGTGCCTGTCACTGCCAGGTGGGGATGGAAACTGAGCTCACTGCTAGATCCTGTGACAGTACCCTACTTAACCTGGTCAACCCCACTGGGTAGGGGAATGGGAGTGCTGCTGCCGGCTTCCATGGGAGCGGGGTAGATGATCACCTCCTGTTCAGCCCCACTGAAACCATGGGGGAGGGGAAGTAACAGTTTT... | GGTGAAAGTAGGACACAGTTGCACCACCTGACTTGCATCACCTCATTGCCTTCTAGTGGCGTTATAAGCTTGGTTCCCTGCTGACTGACACCTGGGAAGGGGTGGTGGGCACCTCAGGGCACCTCTTTGTGCCTGTCACTGCCAGGTGGGGATGGAAACTGAGCTCACTGCTAGATCCTGTGACAGTACCCTACTTAACCTGGTCAACCCCACTGGGTAGGGGAATGGGAGTGCTGCTGCCGGCTTCCATGGGAGCGGGGTAGATGATCACCTCCTGTTCAGCCCCACTGAAACCATGGGGGAGGGGAAGTAACAGTTTT... |
Task1_train_41441 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | TGCCCATCCACAGCCATGAAGAGAGGCATCTACGACAAGTTTGGAGAAGAGGGCCTGAAGGGTGGGATTCCTTTGGAGTTTGGATCCCAGACCCCATGGACAACTGGTTACGTCTTCCATGGCAAACCTGAAAAGGTGTTCCACGAGTTCTTTGGTGGAAACAACCCCTTCAGTGGTAAGAGGTCTTCCTCCCCCACCTTGCCTTATAGAGAAAGGACACTGCTATAAGTGATGTTTTCGTTGAGTAGTTTTGTTTTTATTTTTACTTTATTATTTTATTTTATTTACTTATTTTTTTTGGAGATGGAGACTCACTCTGT... | TGCCCATCCACAGCCATGAAGAGAGGCATCTACGACAAGTTTGGAGAAGAGGGCCTGAAGGGTGGGATTCCTTTGGAGTTTGGATCCCAGACCCCATGGACAACTGGTTACGTCTTCCATGGCAAACCTGAAAAGGTGTTCCACGAGTTCTTTGGTGGAAACAACCCCTTCAGTGGTAAGAGGTCTTCCTCCCCCACCTTGCCTTATAGAGAAAGGACACTGCTATAAGTGATGTTTTCGTTGAGTAGTTTTGTTTTTATTTTTACTTTATTATTTTATTTTATTTACTTATTTTTTTTGGAGATGGAGACTCACTCTGT... |
Task1_train_41442 | A mutation on Chromosome 11 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | AGCCATTAATCACCCCACTGCACTCCAGCCTGGGCAACCGAGCAAGACCCTGTCTCAAAAAACAAACAAGAGGATGGGGCGCAGAGGCTCACACCTGTAATCCCAGCACATTGGGAGGCCAAGGTGGGCAGATCACTTGAGGCCAGGAGTTCGAGACCAGCCTGGCTAACATGGTGAAACTCCATCTCTACTAAAAATACAAAAATTAGCCAGTGTGCTGGTGCACACCTGTCATCCCAGCTACTCGGGAGGCTGAGGCACAAGAATCGCTTGAACCCAGGAGGAGAAGGTTGCAGTGAGCTGAGATTACACGGGTAACA... | AGCCATTAATCACCCCACTGCACTCCAGCCTGGGCAACCGAGCAAGACCCTGTCTCAAAAAACAAACAAGAGGATGGGGCGCAGAGGCTCACACCTGTAATCCCAGCACATTGGGAGGCCAAGGTGGGCAGATCACTTGAGGCCAGGAGTTCGAGACCAGCCTGGCTAACATGGTGAAACTCCATCTCTACTAAAAATACAAAAATTAGCCAGTGTGCTGGTGCACACCTGTCATCCCAGCTACTCGGGAGGCTGAGGCACAAGAATCGCTTGAACCCAGGAGGAGAAGGTTGCAGTGAGCTGAGATTACACGGGTAACA... |
Task1_train_41443 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | TCAATCCAATCTACATTTACCAATCCCTTCTCTGTGTAGTGCTAGGTCCTGAGGATGCAGAAAAAGACAAGGTCCCTGACCTGGGGAGCTTATAATTTGGTGGGTAAGGGATTTCCGCCTCCATTTTACAGGTGAAGAAACGTGCACATAAAGATTAAACTATATGTCTATAATCACAAAAATAATTTTGTGGGTCTAGAAGGGTCAAAGTCAGGCTCCCTGACTTCTAGTAGAGGAAGATCTCTAGTCTAGTAAAGCAGCCTGCTTCACCTGCCAGCCGTACAATATTCCCTGCTTGTTGGGATAGCAGGTGAGCTGAT... | TCAATCCAATCTACATTTACCAATCCCTTCTCTGTGTAGTGCTAGGTCCTGAGGATGCAGAAAAAGACAAGGTCCCTGACCTGGGGAGCTTATAATTTGGTGGGTAAGGGATTTCCGCCTCCATTTTACAGGTGAAGAAACGTGCACATAAAGATTAAACTATATGTCTATAATCACAAAAATAATTTTGTGGGTCTAGAAGGGTCAAAGTCAGGCTCCCTGACTTCTAGTAGAGGAAGATCTCTAGTCTAGTAAAGCAGCCTGCTTCACCTGCCAGCCGTACAATATTCCCTGCTTGTTGGGATAGCAGGTGAGCTGAT... |
Task1_train_41444 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | AACGCTTTTACACTGTTGGTGGGAGTGTAAACTAGTTCAGCCACTGTGGAAGACAGTGTGGCGATTCCTCAAGGATCTAGAAATAGAATTACCATTTGACCCAGCCATCCCATGACTGGGTATATACCCAAAGGATTATAAATCATGCTACTATAAAGACACATGCATATGTATGTTTATTGCGGCACTATTCACAATAGCAAAGACTTGGAACCAACCCAAATATCCATCAATGACAGACTGGATTAAGAAAATGTGGCACATATACACCATGGAATACTATGCAGCCATAGAAAGGGATGAGTTCATGTCCTTTGTAG... | AACGCTTTTACACTGTTGGTGGGAGTGTAAACTAGTTCAGCCACTGTGGAAGACAGTGTGGCGATTCCTCAAGGATCTAGAAATAGAATTACCATTTGACCCAGCCATCCCATGACTGGGTATATACCCAAAGGATTATAAATCATGCTACTATAAAGACACATGCATATGTATGTTTATTGCGGCACTATTCACAATAGCAAAGACTTGGAACCAACCCAAATATCCATCAATGACAGACTGGATTAAGAAAATGTGGCACATATACACCATGGAATACTATGCAGCCATAGAAAGGGATGAGTTCATGTCCTTTGTAG... |
Task1_train_41445 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | ATAAATTATATTATTAAATTATATTTATAAAATAAATATAAATGTTCCTCTGGTGGTGGGAAGAACAGGTTACAAGAAATGAGTTTATAAGTAGGAGGCCAGTTAGGAGGCTACCACAGTCATTTAGGCAAGATATGAAAAGGGCCTGAACTAAATAAGGCAGTAAGGGACGCACAAAAAAGGTGATTGATATGTTTAATACATAATAGGAGGTAAAATAAATAAAACTTTCACTTTCAATGTAAGTAGTGATTAGAAATATGAGATACAATGGGTCATAAGATCCTAATAACAGACTTCAGTAAAAACTGGACAAGAGT... | ATAAATTATATTATTAAATTATATTTATAAAATAAATATAAATGTTCCTCTGGTGGTGGGAAGAACAGGTTACAAGAAATGAGTTTATAAGTAGGAGGCCAGTTAGGAGGCTACCACAGTCATTTAGGCAAGATATGAAAAGGGCCTGAACTAAATAAGGCAGTAAGGGACGCACAAAAAAGGTGATTGATATGTTTAATACATAATAGGAGGTAAAATAAATAAAACTTTCACTTTCAATGTAAGTAGTGATTAGAAATATGAGATACAATGGGTCATAAGATCCTAATAACAGACTTCAGTAAAAACTGGACAAGAGT... |
Task1_train_41446 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | ACAAGTTCTTTACCAAATATATGATTTGCAAATATTTTCTCCTAGTTGGTGGCTTGTCTTTTCCTTTTCTAATGATGTTTTTTGAAAAGCAAAGAATTTTAATTTGATAAGGTCCAATTTATCAGTTGTTTTCTTCTTTTATGGATCATACTTTGGTGTCATATCTAAGAAATCTTTGCCTAACCTGTGGTCACAAAAATTTTCTCTTATGTTTTCTTCTAGAAGTTTTATAGTTTTACATTTACATCTATGACCCATTTTGTGTTAATTTTCATATATGGTGTAAGGTAAGGGTGTAAAGTCATTATTATTTTGCAGAT... | ACAAGTTCTTTACCAAATATATGATTTGCAAATATTTTCTCCTAGTTGGTGGCTTGTCTTTTCCTTTTCTAATGATGTTTTTTGAAAAGCAAAGAATTTTAATTTGATAAGGTCCAATTTATCAGTTGTTTTCTTCTTTTATGGATCATACTTTGGTGTCATATCTAAGAAATCTTTGCCTAACCTGTGGTCACAAAAATTTTCTCTTATGTTTTCTTCTAGAAGTTTTATAGTTTTACATTTACATCTATGACCCATTTTGTGTTAATTTTCATATATGGTGTAAGGTAAGGGTGTAAAGTCATTATTATTTTGCAGAT... |
Task1_train_41447 | An alteration has been detected on Chromosome 11. Is it pathogenic, and if so, what disease is involved? | Benign | AATATTTGTTGATTGGATAAATATGCAAAAATGGAATATGGGTACTATTCTACACAATAAACTACAGATTTTCCAAAATACATTATGTCCCCAGAATCTTGAGACCACATCAGAACATTACAAATGGAAATTTGGGCTAATAATCATCACAACAACAATAACAAAATGAATATAATCAGCATCTATGGCATTTAAGTATTTGTTGAGCAGCCACAACATAGGCAGCAACTTGGTGAGGCAAAAAAGTACATCAGAAAGGAACATGCCATGTACAACACAATGATGACATAAAACAGTAATAGGAGGAAGGCACACTATGT... | AATATTTGTTGATTGGATAAATATGCAAAAATGGAATATGGGTACTATTCTACACAATAAACTACAGATTTTCCAAAATACATTATGTCCCCAGAATCTTGAGACCACATCAGAACATTACAAATGGAAATTTGGGCTAATAATCATCACAACAACAATAACAAAATGAATATAATCAGCATCTATGGCATTTAAGTATTTGTTGAGCAGCCACAACATAGGCAGCAACTTGGTGAGGCAAAAAAGTACATCAGAAAGGAACATGCCATGTACAACACAATGATGACATAAAACAGTAATAGGAGGAAGGCACACTATGT... |
Task1_train_41448 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | GAGACCCCATTTCTAAAAAAAAAAAAATTTTTTTTAATTAGCCGGGCGTGGTGGCATGTGCCTGTAGTCCCAGCTACTCGGCAGGCTAAGGCAGAAAGATCACTTGAGCCCAGGAGTTCAAGGCTGCAGTGAGTGCAGTGAGCGGAGATCGCGCCACTGCACTCCAGCCTGGACAACACGGTGAGACCCTGTTTAAAAAAAAAAAAAAAAATCAATCAGGAGACTCATTAGGAAAAGTACAGTTAAAACTGGCACCTAAAGAGAACAAAAAGTCTTGCTACTCCAAGTGTGGTCCACAGACCAGCAGCATTAGTATCACC... | GAGACCCCATTTCTAAAAAAAAAAAAATTTTTTTTAATTAGCCGGGCGTGGTGGCATGTGCCTGTAGTCCCAGCTACTCGGCAGGCTAAGGCAGAAAGATCACTTGAGCCCAGGAGTTCAAGGCTGCAGTGAGTGCAGTGAGCGGAGATCGCGCCACTGCACTCCAGCCTGGACAACACGGTGAGACCCTGTTTAAAAAAAAAAAAAAAAATCAATCAGGAGACTCATTAGGAAAAGTACAGTTAAAACTGGCACCTAAAGAGAACAAAAAGTCTTGCTACTCCAAGTGTGGTCCACAGACCAGCAGCATTAGTATCACC... |
Task1_train_41449 | A genomic change on Chromosome 11 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TACAGTGTGAGAAATTATTCTTATCCTTCCTCCAGTCTTTGGCCTAGCTCAGGGTAACCCAACTAAAAACTGCTAAATTATCAAACTTGGGGAATCAAACCCAGGAAGGTAAGATCCCATTTTATTCTTAGAAGGTTCTTCCCTTTTCCCTTTATTGCAGAAAGAACCCAGGTCTCTTGAGAATGAAAAAGCACTACATCACATCACCTTCACCTGGGCCATTCAGAGATTTGATTCCCACAAAATCAAAGGAACTAGAGCCCAGAATTGCTCAGTTAGACACAGTATTGAGGAAGCAACAATTGAGAAATGACAATCTA... | TACAGTGTGAGAAATTATTCTTATCCTTCCTCCAGTCTTTGGCCTAGCTCAGGGTAACCCAACTAAAAACTGCTAAATTATCAAACTTGGGGAATCAAACCCAGGAAGGTAAGATCCCATTTTATTCTTAGAAGGTTCTTCCCTTTTCCCTTTATTGCAGAAAGAACCCAGGTCTCTTGAGAATGAAAAAGCACTACATCACATCACCTTCACCTGGGCCATTCAGAGATTTGATTCCCACAAAATCAAAGGAACTAGAGCCCAGAATTGCTCAGTTAGACACAGTATTGAGGAAGCAACAATTGAGAAATGACAATCTA... |
Task1_train_41450 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | GGTTTTTGTGTGAACTAAGTTTTCATCTCTCCGGAATAAATGCCCAGGAGTGCAGTTGCTGGGTTGCATGGTAGTTACATGTTTCGTTTTTTAAGAAACTGCCAAAATGCTTTCCAGAGCGGCTGTACCATTTTACATACCCACCACCAGTGTATGAATGATCAAGTTTGTCTGCATCCTCATGAGCATTAGCTTTTATTTTAGCCATTCTAATAGGTGTGTGGTGGTGTCTTATTGTGATTTTAATTTGTATTTCCCTATTGACTAATGATGTAAGACATCTTTTCATGTGCTTATCTTCCATGTGTATATTCCCTTCA... | GGTTTTTGTGTGAACTAAGTTTTCATCTCTCCGGAATAAATGCCCAGGAGTGCAGTTGCTGGGTTGCATGGTAGTTACATGTTTCGTTTTTTAAGAAACTGCCAAAATGCTTTCCAGAGCGGCTGTACCATTTTACATACCCACCACCAGTGTATGAATGATCAAGTTTGTCTGCATCCTCATGAGCATTAGCTTTTATTTTAGCCATTCTAATAGGTGTGTGGTGGTGTCTTATTGTGATTTTAATTTGTATTTCCCTATTGACTAATGATGTAAGACATCTTTTCATGTGCTTATCTTCCATGTGTATATTCCCTTCA... |
Task1_train_41451 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | CATGTGCTTATCTTCCATGTGTATATTCCCTTCAGTGAAATGTCTGTTCATGTCTTTTGCCCATTTTCTAATTAATTGTTTTTCGTACTGTTGAGTTTTGAGATATCTTTATATATTCTAGATATTAGCCCTTTGTCAAATATGTGCTTTGTAAACAGTTTCTCACAGTGTATGGCTTGTATTTTCATCCTCTTAACCGTATCTTTTGCAGAGCAAAAGTTTGTCATTGTGATAAGGTCCAATTTATCCACTTTTCCTTTTATTGATGCTTTTGGTTTAATAACTCTTTGCCCAGCCCTAGATCCTGAAGACATTCTACT... | CATGTGCTTATCTTCCATGTGTATATTCCCTTCAGTGAAATGTCTGTTCATGTCTTTTGCCCATTTTCTAATTAATTGTTTTTCGTACTGTTGAGTTTTGAGATATCTTTATATATTCTAGATATTAGCCCTTTGTCAAATATGTGCTTTGTAAACAGTTTCTCACAGTGTATGGCTTGTATTTTCATCCTCTTAACCGTATCTTTTGCAGAGCAAAAGTTTGTCATTGTGATAAGGTCCAATTTATCCACTTTTCCTTTTATTGATGCTTTTGGTTTAATAACTCTTTGCCCAGCCCTAGATCCTGAAGACATTCTACT... |
Task1_train_41452 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GAAAAAGTAATTCTAAGGCTGCTTTTTGTCTGTCTGGCTTGATTCCCCTTTTGGACCTCTGAGAAGTGGAACACCTGGTTTTCTTTAAGAAGAATACTTGGAGACTCCATTGTGAGCATTATGGCAGGGTAGCCAACCTGTAAAATGGTGGGTAAAATATAACAAAGCCGGCCGGGCACGGTGGCTCATGCCTGTAATACCAGCACTTTGGGAGGCCAAGGTGGGTGGATCACCTGAGGTCAGGAGTTGGAGACCAGCCTGGCCAACATGGTGAAACCCGTCTCTGCTAAAAATACAAAAAATTAGCTGGGCGTGCTGGC... | GAAAAAGTAATTCTAAGGCTGCTTTTTGTCTGTCTGGCTTGATTCCCCTTTTGGACCTCTGAGAAGTGGAACACCTGGTTTTCTTTAAGAAGAATACTTGGAGACTCCATTGTGAGCATTATGGCAGGGTAGCCAACCTGTAAAATGGTGGGTAAAATATAACAAAGCCGGCCGGGCACGGTGGCTCATGCCTGTAATACCAGCACTTTGGGAGGCCAAGGTGGGTGGATCACCTGAGGTCAGGAGTTGGAGACCAGCCTGGCCAACATGGTGAAACCCGTCTCTGCTAAAAATACAAAAAATTAGCTGGGCGTGCTGGC... |
Task1_train_41453 | A variant found on Chromosome 11 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GAGCACCCAGCCCCTCCCCGTCTGTCCCAGGTCCCACCCTCGCTGATCTCTCCCCCATCTCCCCTCCCTCCTCCCCCTTTCATTCTCTGCCCCTCTTTTCCCACATAGGGAGGCAACTCTGCTCTCTAGCCTGGGGCCTCCTGTGTGCGGAGCCTTGTTCTAGGCACTGCAGCGGGGGTTTAGCCACCTCCTCAGGAAGTCCCTGGTCTGAGGAGGGAGCCAGGTCCTCAATCAAATGATTTTTAGAGTAAAAAGTAAATGGATATTTTATCACAATTTTTTAAATAGTGCAGAAAAAGTCAGCTCATCTCACACACCCC... | GAGCACCCAGCCCCTCCCCGTCTGTCCCAGGTCCCACCCTCGCTGATCTCTCCCCCATCTCCCCTCCCTCCTCCCCCTTTCATTCTCTGCCCCTCTTTTCCCACATAGGGAGGCAACTCTGCTCTCTAGCCTGGGGCCTCCTGTGTGCGGAGCCTTGTTCTAGGCACTGCAGCGGGGGTTTAGCCACCTCCTCAGGAAGTCCCTGGTCTGAGGAGGGAGCCAGGTCCTCAATCAAATGATTTTTAGAGTAAAAAGTAAATGGATATTTTATCACAATTTTTTAAATAGTGCAGAAAAAGTCAGCTCATCTCACACACCCC... |
Task1_train_41454 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | CACGGCAGTGGGACGGGAGGAGCAGAAAAGAGGATTGCGGGGGTAAGGGAGGCTTCAGGCGAGCGCGCTGTCTGCGAGGTGGCCCGGGCACAGGGCTTGGTGCACGGTGGGTTTTTAGACAGAACTGGAGAAGGGATGGCAAGAGGGAGAAAGAGGAACAGAAGGAGGAGGAAGACCACACCAGAATTACCTGATCAAGTGATAGCTGTGAGATGCCAGAGTGCAGCAGAGAGAGGGGGAGGGGGAGAGAGGAGGGACATGCGCCGATCAGAGCAGGATGGGACAGAGAGAGAACATCAGTCAAGAATAAAATCCCAGCC... | CACGGCAGTGGGACGGGAGGAGCAGAAAAGAGGATTGCGGGGGTAAGGGAGGCTTCAGGCGAGCGCGCTGTCTGCGAGGTGGCCCGGGCACAGGGCTTGGTGCACGGTGGGTTTTTAGACAGAACTGGAGAAGGGATGGCAAGAGGGAGAAAGAGGAACAGAAGGAGGAGGAAGACCACACCAGAATTACCTGATCAAGTGATAGCTGTGAGATGCCAGAGTGCAGCAGAGAGAGGGGGAGGGGGAGAGAGGAGGGACATGCGCCGATCAGAGCAGGATGGGACAGAGAGAGAACATCAGTCAAGAATAAAATCCCAGCC... |
Task1_train_41455 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | CAGACGTGGGCTTCTCAGGGTAGGAAGATCAAGAAATGAAGTAGGGTCTTGAAGCAAGCAAGCCATAGCAGAACTAGAAAACTACATCCTGCCTTTGTTTTTTATGTCTCCTGCTTATTTGTTTCCCCTCTTTTCTTTTGCTCCCCGCTTGGTAGCAGCATAAAAACATAGTGAACATTCTACCATCTCATGGCTATTCAAGGAAAAGGATTTATGTCCTTGTTTGACCAAGAGCTCAAAGGAAGTGCTGTACTCCTGGGTTCCCAGTGTGGTTGTTGTGATAGCAATAAACCAAGAGAGAGATGCCAAGTGGGAGGTGG... | CAGACGTGGGCTTCTCAGGGTAGGAAGATCAAGAAATGAAGTAGGGTCTTGAAGCAAGCAAGCCATAGCAGAACTAGAAAACTACATCCTGCCTTTGTTTTTTATGTCTCCTGCTTATTTGTTTCCCCTCTTTTCTTTTGCTCCCCGCTTGGTAGCAGCATAAAAACATAGTGAACATTCTACCATCTCATGGCTATTCAAGGAAAAGGATTTATGTCCTTGTTTGACCAAGAGCTCAAAGGAAGTGCTGTACTCCTGGGTTCCCAGTGTGGTTGTTGTGATAGCAATAAACCAAGAGAGAGATGCCAAGTGGGAGGTGG... |
Task1_train_41456 | Chromosome 11 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AAGGAAGACAGAGCCAGTCTATAAAAGAGGCTGGCTGTGGAGGTAGACAGCAGCTGTTCAGTTCAAGAGACTGAAATCAACAAAACACTAGAACAAGAAGGTCATAGAAAATGATATCCAAATGGTCAGTAAGCATATTAAAATGTGCTTATATTTATTAGTTGTTAGGAAAATGCTATAACCACAATGAAGGACCACTACACACCCACCAAAATTCAGAACTCGGAATTCTTATATAAGGCTATGGGAGTGTAGATTTGTACAACCACTTTGGAAAACTCTATGGCTATCTACCATGAGACCCATCAATTCTATTTCCA... | AAGGAAGACAGAGCCAGTCTATAAAAGAGGCTGGCTGTGGAGGTAGACAGCAGCTGTTCAGTTCAAGAGACTGAAATCAACAAAACACTAGAACAAGAAGGTCATAGAAAATGATATCCAAATGGTCAGTAAGCATATTAAAATGTGCTTATATTTATTAGTTGTTAGGAAAATGCTATAACCACAATGAAGGACCACTACACACCCACCAAAATTCAGAACTCGGAATTCTTATATAAGGCTATGGGAGTGTAGATTTGTACAACCACTTTGGAAAACTCTATGGCTATCTACCATGAGACCCATCAATTCTATTTCCA... |
Task1_train_41457 | A variant was discovered on Chromosome 11. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | ACATCTTTGTGATCCAGCTCTGAGAAAAGATCCAAGGTGTTTTTCAGGCTTCTGAACACCCTGGAAAGATAGTATGCTTACATTTTGTTTAAAAAATTTAAAATGCAACTACTATATGCCAGGTCCTGTGTGGGCACTTTACATATGTTGATTTACTTTAATCCCTACAGCAATCCTATTACTATTTTAAAGCTGAGAGAGGGGAAGTGACTTGCCTTGGGATACATAGCTCAAAGGTGGTAGAGCCAAGATTCCAAAGTGCCTGATTCCTATTGTGTCTGACTCTAAAACACTATGTTCTTTCTGCTATGTTCATCCAG... | ACATCTTTGTGATCCAGCTCTGAGAAAAGATCCAAGGTGTTTTTCAGGCTTCTGAACACCCTGGAAAGATAGTATGCTTACATTTTGTTTAAAAAATTTAAAATGCAACTACTATATGCCAGGTCCTGTGTGGGCACTTTACATATGTTGATTTACTTTAATCCCTACAGCAATCCTATTACTATTTTAAAGCTGAGAGAGGGGAAGTGACTTGCCTTGGGATACATAGCTCAAAGGTGGTAGAGCCAAGATTCCAAAGTGCCTGATTCCTATTGTGTCTGACTCTAAAACACTATGTTCTTTCTGCTATGTTCATCCAG... |
Task1_train_41458 | Assess the clinical impact of this variant found on Chromosome 11. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GTGTGAGTGAGGGGATCAGGAAGGGTGACAAGAGATGATTTGTACGGGAGAAATTCTTAGAGAAGCTCAAGATTGGAAGGGACTTAAAAGTTCTGTGATTTAATCCTCCCAATCCCCTTCCTAGCATCTCTATCACATTGTCATTCTTCCCGGGTGCAGCTCAGAGGCCATCTCTTCTATTACCTTCCACTTCAGTTCCTCTGGCCTATGCTTCAGGCATTTCCCATTATTTAATTTTACGAAAGAAAATTCAGTGTCCGCTGCATGCCAGGCACTGTGCTTAGAATAGGTCCTCAATTGCAGTATGCCCTCCTGTGCCT... | GTGTGAGTGAGGGGATCAGGAAGGGTGACAAGAGATGATTTGTACGGGAGAAATTCTTAGAGAAGCTCAAGATTGGAAGGGACTTAAAAGTTCTGTGATTTAATCCTCCCAATCCCCTTCCTAGCATCTCTATCACATTGTCATTCTTCCCGGGTGCAGCTCAGAGGCCATCTCTTCTATTACCTTCCACTTCAGTTCCTCTGGCCTATGCTTCAGGCATTTCCCATTATTTAATTTTACGAAAGAAAATTCAGTGTCCGCTGCATGCCAGGCACTGTGCTTAGAATAGGTCCTCAATTGCAGTATGCCCTCCTGTGCCT... |
Task1_train_41459 | A variant has been detected on Chromosome 11. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CCATCTCTTCTATTACCTTCCACTTCAGTTCCTCTGGCCTATGCTTCAGGCATTTCCCATTATTTAATTTTACGAAAGAAAATTCAGTGTCCGCTGCATGCCAGGCACTGTGCTTAGAATAGGTCCTCAATTGCAGTATGCCCTCCTGTGCCTCCTGTTGTTTATTTATTTATTTATGCAACGAATGTACACCGAATGCCTATTATATGCCAGGTAATGTTCTAGATGTTGTAACAGAGTGGAGGAAAATACAGCCAGGATCTCAGGCTCTCACGGACCTGTCATTCTAGTAGGAGAGATATAAAATAAACAAATGAAAA... | CCATCTCTTCTATTACCTTCCACTTCAGTTCCTCTGGCCTATGCTTCAGGCATTTCCCATTATTTAATTTTACGAAAGAAAATTCAGTGTCCGCTGCATGCCAGGCACTGTGCTTAGAATAGGTCCTCAATTGCAGTATGCCCTCCTGTGCCTCCTGTTGTTTATTTATTTATTTATGCAACGAATGTACACCGAATGCCTATTATATGCCAGGTAATGTTCTAGATGTTGTAACAGAGTGGAGGAAAATACAGCCAGGATCTCAGGCTCTCACGGACCTGTCATTCTAGTAGGAGAGATATAAAATAAACAAATGAAAA... |
Task1_train_41460 | Given this context: Chromosome 11 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CTGCTTTCCCCTTAGGCCTTCACGGAGCACCTATCGTGTGCCAGGGGGTGGGGCTCTCTCCTTTCTCCCCCAGCCCTACCCCATGAAATAGGTGTTTAGAATTTCCCTTTGCAGACTGGGAGCCAGGAGCAGGAATGGGGAGGTGAGAGGGCACGGACCAGAGAAACGGAAGAATCTCCAGGAGGCAGAGCTGCCAACGCTGGGCCCAGGGGCTGCAGGGCCAAGGGGAGGGGTCCAGGCTGACTCGGGGTGGGCAGGAGAAGCATCACTGAGCAGGAGCTTGGGGGAGAGGCAGTCAGGGAAGGGAAGGGCAAAGGCGC... | CTGCTTTCCCCTTAGGCCTTCACGGAGCACCTATCGTGTGCCAGGGGGTGGGGCTCTCTCCTTTCTCCCCCAGCCCTACCCCATGAAATAGGTGTTTAGAATTTCCCTTTGCAGACTGGGAGCCAGGAGCAGGAATGGGGAGGTGAGAGGGCACGGACCAGAGAAACGGAAGAATCTCCAGGAGGCAGAGCTGCCAACGCTGGGCCCAGGGGCTGCAGGGCCAAGGGGAGGGGTCCAGGCTGACTCGGGGTGGGCAGGAGAAGCATCACTGAGCAGGAGCTTGGGGGAGAGGCAGTCAGGGAAGGGAAGGGCAAAGGCGC... |
Task1_train_41461 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | GTGACAACACGTATGTAGCACCTGGCATCTGTAGCAGCCACCACTGTAATTGTACAGAGGGAACTGAGATCTGAGGAGGGACACTGGCTCATGCCACAGCATGTGTCAGTGGGAAAAGCCCCTCCTGCACCCTGCCTCTCCACCAGCTACTCTGCCAGTCCTGCTGGAGGCAACGCATATGAATATAGTAATTGGAGTACACCAGGCCTGGGTCCCATTCCTGCCCTGCATTTTACTAGTTTGGGGTAAGGCCCTATTCCTCTCTGAGCCTCTGTTTCTTCATCTGTATAATGGGGGAAGCAGCCTAACTGCCTGCCCGA... | GTGACAACACGTATGTAGCACCTGGCATCTGTAGCAGCCACCACTGTAATTGTACAGAGGGAACTGAGATCTGAGGAGGGACACTGGCTCATGCCACAGCATGTGTCAGTGGGAAAAGCCCCTCCTGCACCCTGCCTCTCCACCAGCTACTCTGCCAGTCCTGCTGGAGGCAACGCATATGAATATAGTAATTGGAGTACACCAGGCCTGGGTCCCATTCCTGCCCTGCATTTTACTAGTTTGGGGTAAGGCCCTATTCCTCTCTGAGCCTCTGTTTCTTCATCTGTATAATGGGGGAAGCAGCCTAACTGCCTGCCCGA... |
Task1_train_41462 | A genomic variant on Chromosome 11 is under review. What is the biological outcome — benign or pathogenic? | Benign | AATGGGGGAAGCAGCCTAACTGCCTGCCCGAGGTTAAAGGAAGAACCAAAGAGGTGTAGTAGCTTAATCTGCTGGTGGCAAGGGACAGAGTAAGGGGGAAAGAGGCTTGGGACAGGTGTCCCCAAAACCCATCTGGGAATCTGGACACCCACGTTGGACACCAGGATGCCCAATGAGAAGGGAAGTTCCTGCCCCTGGATGACAGGCTAGGGGGACAGGGCAGGTGGAGTATGGGTGCGGTGGGGCAGTCACTGCAGGCCCCATTGCAGGGAGGGAGTCCTGGTCTTGAAGGCCAGCCCCGGCCAGACCACAGGTGCTTT... | AATGGGGGAAGCAGCCTAACTGCCTGCCCGAGGTTAAAGGAAGAACCAAAGAGGTGTAGTAGCTTAATCTGCTGGTGGCAAGGGACAGAGTAAGGGGGAAAGAGGCTTGGGACAGGTGTCCCCAAAACCCATCTGGGAATCTGGACACCCACGTTGGACACCAGGATGCCCAATGAGAAGGGAAGTTCCTGCCCCTGGATGACAGGCTAGGGGGACAGGGCAGGTGGAGTATGGGTGCGGTGGGGCAGTCACTGCAGGCCCCATTGCAGGGAGGGAGTCCTGGTCTTGAAGGCCAGCCCCGGCCAGACCACAGGTGCTTT... |
Task1_train_41463 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TTACAGTCCTATTTCTGGATCTGTAAATTTAAGATATTGTCTGTTGTCTTCTAGTTTTGGTGGTTGGGGATTTCACTTTTTTATACCATCCCTGCTTTCCCCACTATATTTTCTCAATAAAGTCAGAGCATAATTTTTTACTAAATAAGTAGTTAGGATGTAACATCCATAATATCAATATGGCTATGTAAATAATGTGCACTGCTAAGCCAGATAGTGTACTCTATGGTAACATTTCTTTCTGTGTAGACTACTAAAAATACAAAAATTAGCTGGGCATGATGGCATGCACCTGTGTTCCCAGCTACTCAGGAGGCTGA... | TTACAGTCCTATTTCTGGATCTGTAAATTTAAGATATTGTCTGTTGTCTTCTAGTTTTGGTGGTTGGGGATTTCACTTTTTTATACCATCCCTGCTTTCCCCACTATATTTTCTCAATAAAGTCAGAGCATAATTTTTTACTAAATAAGTAGTTAGGATGTAACATCCATAATATCAATATGGCTATGTAAATAATGTGCACTGCTAAGCCAGATAGTGTACTCTATGGTAACATTTCTTTCTGTGTAGACTACTAAAAATACAAAAATTAGCTGGGCATGATGGCATGCACCTGTGTTCCCAGCTACTCAGGAGGCTGA... |
Task1_train_41464 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GGAGGGGATGAGGGGGAGGAGGAGGGGGAGGGAGAGAAGGGAGGATAGAGGAGGGAGGAGGGGGAGGAGGAGGGGAGGGGGAGGGGGAAGAGGAGGAGGAGGTTATTAGAGAGGGGGAACTGAGCAAAGGGAACTGAGAAACATGGTCAAAAAGAAAGGAGGAAAGGCAGGAGAGCGTAGAGTCTGTTTTAAGGAGGGAGAAGGAACGGGGCACAGTGGCTCATGCCTGTAATCCCAGCACTTTTCGGGGCTGAGGTGGGAGGATCACTTGAACCCAGGAGTTCAAGACCAGACTGGGCAATATAGTGGGAACCCGTCTC... | GGAGGGGATGAGGGGGAGGAGGAGGGGGAGGGAGAGAAGGGAGGATAGAGGAGGGAGGAGGGGGAGGAGGAGGGGAGGGGGAGGGGGAAGAGGAGGAGGAGGTTATTAGAGAGGGGGAACTGAGCAAAGGGAACTGAGAAACATGGTCAAAAAGAAAGGAGGAAAGGCAGGAGAGCGTAGAGTCTGTTTTAAGGAGGGAGAAGGAACGGGGCACAGTGGCTCATGCCTGTAATCCCAGCACTTTTCGGGGCTGAGGTGGGAGGATCACTTGAACCCAGGAGTTCAAGACCAGACTGGGCAATATAGTGGGAACCCGTCTC... |
Task1_train_41465 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | ATGCTGCTGTCTCAAGGATGCTCCAGGCTGGGAGGAGGCTGTGACTCCCGCAGCCCAGTAATCAGAGGAGGTGTCTTGGAGGTGAAGGGTGATGAGGTTTTTGCCCAAAGGGCCAGGTGGGAAAAGGCAGAGGGAATAGAAACTCACAGGTGGGAGCCCCTCAGGCTCATGTGGGCCTGTGGAGAGCCATGCCTGGGGTGGCAGATCTGGGGCCAAGATGCTCGACCTTGCTCTGTGAGTAGTGAGGTCCCGCGAAGGCAAAGGCTTTCAGCAGCCTGTAACAGGGTCAGATTTGCATTTTCCAAAGTTCCTCCTGATCC... | ATGCTGCTGTCTCAAGGATGCTCCAGGCTGGGAGGAGGCTGTGACTCCCGCAGCCCAGTAATCAGAGGAGGTGTCTTGGAGGTGAAGGGTGATGAGGTTTTTGCCCAAAGGGCCAGGTGGGAAAAGGCAGAGGGAATAGAAACTCACAGGTGGGAGCCCCTCAGGCTCATGTGGGCCTGTGGAGAGCCATGCCTGGGGTGGCAGATCTGGGGCCAAGATGCTCGACCTTGCTCTGTGAGTAGTGAGGTCCCGCGAAGGCAAAGGCTTTCAGCAGCCTGTAACAGGGTCAGATTTGCATTTTCCAAAGTTCCTCCTGATCC... |
Task1_train_41466 | This sequence change occurs on Chromosome 11. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CAGCTCAAGGGTGGTCTCAGTAGTCGTTCTGGAACCAGGCAAGGTCAGGTTCTTAGCACCTTGCAGGGTCTCCCCCAGGGGACCTCTCTTTAGCCACCAGCCGCCAGACTTACTTTACAATCTCTTCCCTCTCTCCTCTGATTCTCTGAGTTTGCTGTTCCCTCTTCCTGGGATGCCCTTTCCCCTAATGTCTGCCTAAAAAAAAAATCTTAAAACCCAGCTGTCACCCCTAACACGACTCCCTTAGTTAACCATGGCTGGCACTCATATACATTTGGTCTAACAGGCACCAATCTAGGTGCATTACGCATCTTAACCTG... | CAGCTCAAGGGTGGTCTCAGTAGTCGTTCTGGAACCAGGCAAGGTCAGGTTCTTAGCACCTTGCAGGGTCTCCCCCAGGGGACCTCTCTTTAGCCACCAGCCGCCAGACTTACTTTACAATCTCTTCCCTCTCTCCTCTGATTCTCTGAGTTTGCTGTTCCCTCTTCCTGGGATGCCCTTTCCCCTAATGTCTGCCTAAAAAAAAAATCTTAAAACCCAGCTGTCACCCCTAACACGACTCCCTTAGTTAACCATGGCTGGCACTCATATACATTTGGTCTAACAGGCACCAATCTAGGTGCATTACGCATCTTAACCTG... |
Task1_train_41467 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | GTGTCTGGCTCTCACTGGGCTGCTCTGATCTTGGCTGTGCTGCGCCTCACTCAGGCTGGGCAGGACTGACCCCGGCGGGGCCCTGTTCTCCGTGTTGGTCCTGCAGGGGAGCGAAAACGACGGCCCCCAGCTTCACGCTGGCCACCATCAAGGGGGACGAATACACCTTCACCTCCAGCAATGCTGAGGACATTCGTGACCTGGTGGTCACCTTCCTAGAGGGGCTCCGGAAGAGATCTAAGTATGTTGTGGCCCTGCAGGATAACCCCAACCCCGGTGAGTGGCTGCTGGTATGGACTGCCTGGCACTGGGGGTCAGGG... | GTGTCTGGCTCTCACTGGGCTGCTCTGATCTTGGCTGTGCTGCGCCTCACTCAGGCTGGGCAGGACTGACCCCGGCGGGGCCCTGTTCTCCGTGTTGGTCCTGCAGGGGAGCGAAAACGACGGCCCCCAGCTTCACGCTGGCCACCATCAAGGGGGACGAATACACCTTCACCTCCAGCAATGCTGAGGACATTCGTGACCTGGTGGTCACCTTCCTAGAGGGGCTCCGGAAGAGATCTAAGTATGTTGTGGCCCTGCAGGATAACCCCAACCCCGGTGAGTGGCTGCTGGTATGGACTGCCTGGCACTGGGGGTCAGGG... |
Task1_train_41468 | Consider this mutation on Chromosome 11. Is this a benign change or a disease-causing variant? | Benign | CCTGGCTCTCCTTCAGCTCAGCTGGATTGTTTCCGCTTCTCAAGTGTGCCACAGGGCCTTTGTAATGTTGGGATGCTCTTCCCTCAGTTCCTTCCCTCACCTACTGAGCTTTTAGATGTCAGTCAGCCATTTTATCTTAAAGGAAGTCTGCCCTGTCCTCAAGCCTAGATTAGGTCACCTTGTTATATTCTCTTACAGCACTGTGGACAATTCCTTCAAAGGTTGTCATTATATATCTGTTTGGTATGATTTTTAATGTCTGTCCTTGCCCTGAGACTACAAGTTCCATGGAAGTAGGGAGGGTAGGCATTGTTGCTTAA... | CCTGGCTCTCCTTCAGCTCAGCTGGATTGTTTCCGCTTCTCAAGTGTGCCACAGGGCCTTTGTAATGTTGGGATGCTCTTCCCTCAGTTCCTTCCCTCACCTACTGAGCTTTTAGATGTCAGTCAGCCATTTTATCTTAAAGGAAGTCTGCCCTGTCCTCAAGCCTAGATTAGGTCACCTTGTTATATTCTCTTACAGCACTGTGGACAATTCCTTCAAAGGTTGTCATTATATATCTGTTTGGTATGATTTTTAATGTCTGTCCTTGCCCTGAGACTACAAGTTCCATGGAAGTAGGGAGGGTAGGCATTGTTGCTTAA... |
Task1_train_41469 | A mutation has occurred on Chromosome 11. What is the medical relevance of this mutation? | Benign | GTTTGCTGTGGCCTTCCCGGTTGTGAGAGCCTGTGATCCTTAGATGTGTCTCCTGTTTCAGACCAGCCCCACCATGCAACTTCCTTTGACTTTCTGTGTACCACTGGGATAGAGGAATCAAGAGGACAATCTAGCTCTCCATACTTTGAACAACCAAATGTGCATTGAATACTCTGAAACCGAAGGGACTGGATCTGCAGGTGGGATGAGGGAGACAGACCACTTTTCTATATTGCAGTGTGAATGCTGGGCCCCTGCTCAAGTCTACCCTGATCACCTCAGGGCATAAAGCATGTTTCATTCTCTGGCCCGACAGTGTC... | GTTTGCTGTGGCCTTCCCGGTTGTGAGAGCCTGTGATCCTTAGATGTGTCTCCTGTTTCAGACCAGCCCCACCATGCAACTTCCTTTGACTTTCTGTGTACCACTGGGATAGAGGAATCAAGAGGACAATCTAGCTCTCCATACTTTGAACAACCAAATGTGCATTGAATACTCTGAAACCGAAGGGACTGGATCTGCAGGTGGGATGAGGGAGACAGACCACTTTTCTATATTGCAGTGTGAATGCTGGGCCCCTGCTCAAGTCTACCCTGATCACCTCAGGGCATAAAGCATGTTTCATTCTCTGGCCCGACAGTGTC... |
Task1_train_41470 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | TGGATCACGAGGTCAAGAGATCGAGACCATCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAGAAAATTAGCTGGGCATGGTGGCGTGCACCTGTAGTCTCAGCCTGAGGCAGGAGAACTGCTTGAATCCAAGAGGCGGAGGTTGCAGCGAGCCAAGATTGGGCCTTTGCACTCCAGCCTGGTGACAGAGCGAGACTCTGTCTCAAAAAAAAAATAAATAAATAAGTCTAACTTATAGAAAAAGAGAGTAGAATGTTGGTTACCAAAGGCTAATGTTGGTTACTGAAAAGTAGAATGTTGGTTACCAAAGG... | TGGATCACGAGGTCAAGAGATCGAGACCATCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAGAAAATTAGCTGGGCATGGTGGCGTGCACCTGTAGTCTCAGCCTGAGGCAGGAGAACTGCTTGAATCCAAGAGGCGGAGGTTGCAGCGAGCCAAGATTGGGCCTTTGCACTCCAGCCTGGTGACAGAGCGAGACTCTGTCTCAAAAAAAAAATAAATAAATAAGTCTAACTTATAGAAAAAGAGAGTAGAATGTTGGTTACCAAAGGCTAATGTTGGTTACTGAAAAGTAGAATGTTGGTTACCAAAGG... |
Task1_train_41471 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | AACTGTTACTGGTTTATATATTTACTACACTACACTTTTTATTGTTATTTTAGAGTATATACATTCTATTATATATTTAAAAAATTAAATGTAAAACAGCCTCAGGTAGTCCTTCAGGAGGTATTCTAGAAGGCATTGTTTTCATAGGAGATGACCGCTCCATGCATGTTATCCCTGCAGACACTGCAGTGGGACAAGATGTGAAGGTAGAAGACAGTGATATGAACGATCCTGACCCTGTGTAAGCCTAGGCTAATGTGTGTGCTTGTTTCTTAGTTTCTAACAAAAAAGTTAAAAAAAAATTAAAATAGAAAACAGCT... | AACTGTTACTGGTTTATATATTTACTACACTACACTTTTTATTGTTATTTTAGAGTATATACATTCTATTATATATTTAAAAAATTAAATGTAAAACAGCCTCAGGTAGTCCTTCAGGAGGTATTCTAGAAGGCATTGTTTTCATAGGAGATGACCGCTCCATGCATGTTATCCCTGCAGACACTGCAGTGGGACAAGATGTGAAGGTAGAAGACAGTGATATGAACGATCCTGACCCTGTGTAAGCCTAGGCTAATGTGTGTGCTTGTTTCTTAGTTTCTAACAAAAAAGTTAAAAAAAAATTAAAATAGAAAACAGCT... |
Task1_train_41472 | A variant found on Chromosome 11 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CCAAAGTGCTGCACCTACAATGGGCCACCCCAGGGGACAAGCTGTTGGGACTGGAATGCGGTGGCAAGAGCCGTGCACTCTGGCTGCTGAAACCTGCTGTTTCCACTGTAAGCTACCACTTAGTGAATATTTTCTACGTATTGGGAACTGTACTAAGTGGCTTTCATGTTTTGTTTTTTGTTTGTTTGACTGGTTTGTTGTTGTTGTTGTTGTTGTTGTTGTTGTTTTTGAGACGGAGTTTCGCTCTTGTTGCCCAGGCTGGAGTACAATGGCGCGATCTAGGCTCACCACAACCTCTGCCTCCCGGGTTCAAGCGATTC... | CCAAAGTGCTGCACCTACAATGGGCCACCCCAGGGGACAAGCTGTTGGGACTGGAATGCGGTGGCAAGAGCCGTGCACTCTGGCTGCTGAAACCTGCTGTTTCCACTGTAAGCTACCACTTAGTGAATATTTTCTACGTATTGGGAACTGTACTAAGTGGCTTTCATGTTTTGTTTTTTGTTTGTTTGACTGGTTTGTTGTTGTTGTTGTTGTTGTTGTTGTTGTTTTTGAGACGGAGTTTCGCTCTTGTTGCCCAGGCTGGAGTACAATGGCGCGATCTAGGCTCACCACAACCTCTGCCTCCCGGGTTCAAGCGATTC... |
Task1_train_41473 | A variant has been detected on Chromosome 11. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | AAATTTAATTTAATTTTTTTTTTTTTTAAATATAGATGGGGTCTCACTATTGTTGCCCAGGCTGGTCTTGAGCTCCTGAGCTCAAATGATCTCCCGCCTCGGCCTCCCAAAATGCTAGGATTACAAATGTGAGCTACCACGTCTGGCCTATTTTTTAATTTTTTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTTGTTCTGTCGCCCAGGCTGAGTGCAGTGGCGCCATCTTGGCTCACTGTAACCTCTGCCTCCCGGGTTCATGCCATTCTCCTGTCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCACCACC... | AAATTTAATTTAATTTTTTTTTTTTTTAAATATAGATGGGGTCTCACTATTGTTGCCCAGGCTGGTCTTGAGCTCCTGAGCTCAAATGATCTCCCGCCTCGGCCTCCCAAAATGCTAGGATTACAAATGTGAGCTACCACGTCTGGCCTATTTTTTAATTTTTTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTTGTTCTGTCGCCCAGGCTGAGTGCAGTGGCGCCATCTTGGCTCACTGTAACCTCTGCCTCCCGGGTTCATGCCATTCTCCTGTCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCACCACC... |
Task1_train_41474 | Chromosome 11 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AGTCACCCAGTTATTCTGGAACTCGGTTAATTCATCTAAAAAAACTGGTTATTATAAAGATAAAAGAACTGGTTATTTAACCAAGAGCCATTTCCCCCATCTTTCTTCCTGAGAGAGCCCTGATTTTACTCAGGTATCAGGCAGGCAGCAAAGTGCTCGGAAAAGGCAGGTCCAGCCCAAGAGCTGAACCACTATTGGTCTAAACCCATCATGGCAATCCCATTCCCATTTTCCAGTGACTGGTTTGCTGGTGGGCAAGTAAGCCAGTTCTAGACAATGGAGCACGAGAGTATGCTGGCTGGGGAGCTTCTCAGGGATGT... | AGTCACCCAGTTATTCTGGAACTCGGTTAATTCATCTAAAAAAACTGGTTATTATAAAGATAAAAGAACTGGTTATTTAACCAAGAGCCATTTCCCCCATCTTTCTTCCTGAGAGAGCCCTGATTTTACTCAGGTATCAGGCAGGCAGCAAAGTGCTCGGAAAAGGCAGGTCCAGCCCAAGAGCTGAACCACTATTGGTCTAAACCCATCATGGCAATCCCATTCCCATTTTCCAGTGACTGGTTTGCTGGTGGGCAAGTAAGCCAGTTCTAGACAATGGAGCACGAGAGTATGCTGGCTGGGGAGCTTCTCAGGGATGT... |
Task1_train_41475 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | ATTTATTTATTGGAGACAAGGTCTCAACTTTGTTGCCCAGGCTGGAGTGCAGTGGTGCAATCGTGGCTCGCTGCAGCCTCAACCTCCTGGGCTCAAGTGATTCTCCTCCCTTAGCTTCCTGAGTACCTGGGACTACAAGTGCACATCACCATGCCTGGCTAATTTTTTAAATTTTTTTGTAGAGACAGGGTCTCACTATGTTGCCCAGGCTGGTCTTGAACTCCTGGCCTCAAGAGATGTTCCTGCCTTGGTCTCCCAAAGTGCTGGGATTACAGGTGTGAACCACAGTGCCTGTGCCTAGTGAGCAAGTTTGTTTAGTT... | ATTTATTTATTGGAGACAAGGTCTCAACTTTGTTGCCCAGGCTGGAGTGCAGTGGTGCAATCGTGGCTCGCTGCAGCCTCAACCTCCTGGGCTCAAGTGATTCTCCTCCCTTAGCTTCCTGAGTACCTGGGACTACAAGTGCACATCACCATGCCTGGCTAATTTTTTAAATTTTTTTGTAGAGACAGGGTCTCACTATGTTGCCCAGGCTGGTCTTGAACTCCTGGCCTCAAGAGATGTTCCTGCCTTGGTCTCCCAAAGTGCTGGGATTACAGGTGTGAACCACAGTGCCTGTGCCTAGTGAGCAAGTTTGTTTAGTT... |
Task1_train_41476 | A mutation is present on Chromosome 11. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | AAAAAAGGGAATAATACCCATTTATTTTAACTATCTTTTTTTTTTTTCTTTTTTTGAGACAGGGTCTCACTCTATTGCCCCAGGCTGGAGTGCAGTGGCGCCATCTTGGCTCACTGCAACCTTCACCTCCCAGGTTCAAAGGATCTTCATGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCACCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGATTTTGCCATGTTGGCCAGGCTGATCTCAAACTCCTGGCATCAAGTGAACCACCGCTTCAGCCTCCGAAAGTACTGGGATTGCAGATGTG... | AAAAAAGGGAATAATACCCATTTATTTTAACTATCTTTTTTTTTTTTCTTTTTTTGAGACAGGGTCTCACTCTATTGCCCCAGGCTGGAGTGCAGTGGCGCCATCTTGGCTCACTGCAACCTTCACCTCCCAGGTTCAAAGGATCTTCATGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCACCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGATTTTGCCATGTTGGCCAGGCTGATCTCAAACTCCTGGCATCAAGTGAACCACCGCTTCAGCCTCCGAAAGTACTGGGATTGCAGATGTG... |
Task1_train_41477 | An alteration has been detected on Chromosome 11. Is it pathogenic, and if so, what disease is involved? | Benign | AATACCCATTTATTTTAACTATCTTTTTTTTTTTTCTTTTTTTGAGACAGGGTCTCACTCTATTGCCCCAGGCTGGAGTGCAGTGGCGCCATCTTGGCTCACTGCAACCTTCACCTCCCAGGTTCAAAGGATCTTCATGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCACCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGATTTTGCCATGTTGGCCAGGCTGATCTCAAACTCCTGGCATCAAGTGAACCACCGCTTCAGCCTCCGAAAGTACTGGGATTGCAGATGTGAGCCACCATGCC... | AATACCCATTTATTTTAACTATCTTTTTTTTTTTTCTTTTTTTGAGACAGGGTCTCACTCTATTGCCCCAGGCTGGAGTGCAGTGGCGCCATCTTGGCTCACTGCAACCTTCACCTCCCAGGTTCAAAGGATCTTCATGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCACCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGATTTTGCCATGTTGGCCAGGCTGATCTCAAACTCCTGGCATCAAGTGAACCACCGCTTCAGCCTCCGAAAGTACTGGGATTGCAGATGTGAGCCACCATGCC... |
Task1_train_41478 | A mutation on Chromosome 11 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TTTTTTTTTCTTTTTTTGAGACAGGGTCTCACTCTATTGCCCCAGGCTGGAGTGCAGTGGCGCCATCTTGGCTCACTGCAACCTTCACCTCCCAGGTTCAAAGGATCTTCATGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCACCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGATTTTGCCATGTTGGCCAGGCTGATCTCAAACTCCTGGCATCAAGTGAACCACCGCTTCAGCCTCCGAAAGTACTGGGATTGCAGATGTGAGCCACCATGCCTGGCCAATTATCTTAAAGATTATTGT... | TTTTTTTTTCTTTTTTTGAGACAGGGTCTCACTCTATTGCCCCAGGCTGGAGTGCAGTGGCGCCATCTTGGCTCACTGCAACCTTCACCTCCCAGGTTCAAAGGATCTTCATGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCACCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGATTTTGCCATGTTGGCCAGGCTGATCTCAAACTCCTGGCATCAAGTGAACCACCGCTTCAGCCTCCGAAAGTACTGGGATTGCAGATGTGAGCCACCATGCCTGGCCAATTATCTTAAAGATTATTGT... |
Task1_train_41479 | A mutation is present on Chromosome 11. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | ATGATCTCAACACCATTGCACTCCATCCTGGGTGACAGTGAGACCCTGTCTCTAAAAATAAGTAGGGGTTTGAATAGGAATGGTGAGAAGGGGGGAAAAAAAGCAGGGTTAACTGCTGCTGCTGAATAGTTTTTTAATTAAGGCAAAAATTACCTTTATAGAGTGTCTACATATTTTATTTTTTCCCCAGGAAAGGATCAATAACCTCATTACCACAAGGAGCTTTTATAAGGAAAACAGTCTGTTTACTGCACTAAAGCCTCAGTCCCAAGAACTGCTCCCCCTGTTCATCCTGAAAGCTGAAATGCAGGACTGGAGAA... | ATGATCTCAACACCATTGCACTCCATCCTGGGTGACAGTGAGACCCTGTCTCTAAAAATAAGTAGGGGTTTGAATAGGAATGGTGAGAAGGGGGGAAAAAAAGCAGGGTTAACTGCTGCTGCTGAATAGTTTTTTAATTAAGGCAAAAATTACCTTTATAGAGTGTCTACATATTTTATTTTTTCCCCAGGAAAGGATCAATAACCTCATTACCACAAGGAGCTTTTATAAGGAAAACAGTCTGTTTACTGCACTAAAGCCTCAGTCCCAAGAACTGCTCCCCCTGTTCATCCTGAAAGCTGAAATGCAGGACTGGAGAA... |
Task1_train_41480 | A variant on Chromosome 11 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GGGCCTCGCTGTTGCTCAGGCTGGTCTTGAACTCCTGGGCTCAAGGGATCCTGCTGCCTGGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGTCACCACGCAGGCCCCTGGCATTTATTATGTGCCAAGTGTTGTGCTTTATTTCATCAGGATAGCTCTCAGTGAAATGACGCCCTTGCCCCATTTCACAGATGAGAAAACTGAGGCCCAGAAAGTTTGAGTTGCTTGCCCTAAGTCTCAGCACTCGGGGACTGCACCGGGAACTCTTGAGCCCCGCGGTTGTCGGGCTGTGACCTCATTCCCTGTCCTCCGCAGCGCG... | GGGCCTCGCTGTTGCTCAGGCTGGTCTTGAACTCCTGGGCTCAAGGGATCCTGCTGCCTGGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGTCACCACGCAGGCCCCTGGCATTTATTATGTGCCAAGTGTTGTGCTTTATTTCATCAGGATAGCTCTCAGTGAAATGACGCCCTTGCCCCATTTCACAGATGAGAAAACTGAGGCCCAGAAAGTTTGAGTTGCTTGCCCTAAGTCTCAGCACTCGGGGACTGCACCGGGAACTCTTGAGCCCCGCGGTTGTCGGGCTGTGACCTCATTCCCTGTCCTCCGCAGCGCG... |
Task1_train_41481 | A mutation on Chromosome 11 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CCCTCTGCCATTCTTTCCATCCCGTGTGCAGATCCACCGTCTTCGTAGGGCCTTCCTGGATTCCTTGCCTTTAGTGGGTAAGAGTGTGGGCTCTCGAGGTAAGTTGCTAGAGGTCAAATCCCGCCTCTACCACTTCTTGCCTGTGCGACCTTGGACAAGTTACTCAACCTCTCTGTTTGAGTTTCCTCAACTGTAAAATGGAGTATAACCAAACCCATCATCTAGGGTTGTTGTGAGGATTAAATTGGGTAAAACAAGATAATACACGAAACATGTCTAGAACTGTGCTGTGGGAGACGCCGTTATCATTGTTATGACTT... | CCCTCTGCCATTCTTTCCATCCCGTGTGCAGATCCACCGTCTTCGTAGGGCCTTCCTGGATTCCTTGCCTTTAGTGGGTAAGAGTGTGGGCTCTCGAGGTAAGTTGCTAGAGGTCAAATCCCGCCTCTACCACTTCTTGCCTGTGCGACCTTGGACAAGTTACTCAACCTCTCTGTTTGAGTTTCCTCAACTGTAAAATGGAGTATAACCAAACCCATCATCTAGGGTTGTTGTGAGGATTAAATTGGGTAAAACAAGATAATACACGAAACATGTCTAGAACTGTGCTGTGGGAGACGCCGTTATCATTGTTATGACTT... |
Task1_train_41482 | A variant on Chromosome 11 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TGCCCAATCTTTCCCTTTGGCAATTCAGTCCATCCATCGCATTATGGTGTTGCCATAGTCCATTTTATGCTGCTAAAACCAAATACTCGAGGCTTGGTGATTTATGAAGAAATTTATTTCTCAGTTTTGGAAGCTGGGAGGCCCAAGATCGAGGGGCTGTGTCTGGTGACGGCCTTCTTGCTGCATTATAATGTGGGTAGAAGGCATCACAGGGTGTGAGAGCATGCATGAGAGAAGGGAAAGCGGGATGAACTCACCCTTTTATCAGGAACCTGCTCCTGTCTCCATTTGTGGCTGCTGGGGAAAGCAAACGGCCTGTG... | TGCCCAATCTTTCCCTTTGGCAATTCAGTCCATCCATCGCATTATGGTGTTGCCATAGTCCATTTTATGCTGCTAAAACCAAATACTCGAGGCTTGGTGATTTATGAAGAAATTTATTTCTCAGTTTTGGAAGCTGGGAGGCCCAAGATCGAGGGGCTGTGTCTGGTGACGGCCTTCTTGCTGCATTATAATGTGGGTAGAAGGCATCACAGGGTGTGAGAGCATGCATGAGAGAAGGGAAAGCGGGATGAACTCACCCTTTTATCAGGAACCTGCTCCTGTCTCCATTTGTGGCTGCTGGGGAAAGCAAACGGCCTGTG... |
Task1_train_41483 | A variant on Chromosome 11 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | CTCTGTGTGGGGGCACAGAAATGAGTAATCCCTCCCTGGCTCATGGAGGGAAGGGAAAGGTCAGTGAGGGAGGGTTGGGAAGATGACATGGAAGAGGCAGCGCTGTATCTGGGACTCATCTTGACGGGAGAGAATGGCAGTGAGTGGAGGCAGGGAGAGAATGTTTGAGGTGTGCCAGGAAGAGAAGATTCCTAGAGCCTCGTTCATTTCTCTGAGCCCAATGCCCTGCTCAGCCCTGCTCAGAGGCGTGGACATGTGGGCTGGGTTGGGTCAGGGACAATAGAAAAGCGGGGAGGACCTCATGGAGGAGGCCAGGAAGT... | CTCTGTGTGGGGGCACAGAAATGAGTAATCCCTCCCTGGCTCATGGAGGGAAGGGAAAGGTCAGTGAGGGAGGGTTGGGAAGATGACATGGAAGAGGCAGCGCTGTATCTGGGACTCATCTTGACGGGAGAGAATGGCAGTGAGTGGAGGCAGGGAGAGAATGTTTGAGGTGTGCCAGGAAGAGAAGATTCCTAGAGCCTCGTTCATTTCTCTGAGCCCAATGCCCTGCTCAGCCCTGCTCAGAGGCGTGGACATGTGGGCTGGGTTGGGTCAGGGACAATAGAAAAGCGGGGAGGACCTCATGGAGGAGGCCAGGAAGT... |
Task1_train_41484 | Located on Chromosome 11, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TGTCTTGAAAGCCCATATCATTCATAATCAATTGGTGCAATTCATTACTATTATCAACGTGCTACTTCCATCTAGCAGAGTAGTAAAGATTTACAAAAAATTTGAAAGAAAATTATGGCTCCACATTGAAATATGTCTACACTGCTCACATTCATGTTACAAGATTAAGACAGACACATCCTTTCAGACAAAAATCAAAGTTTTAATTAAAAAGATAACAGAGAAGCTAAAAAAGAGCTACACTGGCAGCCTGTTTCTTTCAGTCTCATCCATTCTAAGTCTTGTACAAATACAAACTTTTATGTCGTATAGAAACAAGC... | TGTCTTGAAAGCCCATATCATTCATAATCAATTGGTGCAATTCATTACTATTATCAACGTGCTACTTCCATCTAGCAGAGTAGTAAAGATTTACAAAAAATTTGAAAGAAAATTATGGCTCCACATTGAAATATGTCTACACTGCTCACATTCATGTTACAAGATTAAGACAGACACATCCTTTCAGACAAAAATCAAAGTTTTAATTAAAAAGATAACAGAGAAGCTAAAAAAGAGCTACACTGGCAGCCTGTTTCTTTCAGTCTCATCCATTCTAAGTCTTGTACAAATACAAACTTTTATGTCGTATAGAAACAAGC... |
Task1_train_41485 | Consider this mutation on Chromosome 11. Is this a benign change or a disease-causing variant? | Benign | TGGAAGAAATCCAATAGACATTAGCTTTCTGGAGTTGCAAAAGTTCTTTTCATCATTAACAGTACTCGTTCTATTTCCTGTGGTGCTTTCTTAAGAAAGGCTTTATTCAGAAGAAAATGACTTACTGATAGCATTTAAAGTTGCATCTACCATTGGTTAATACTCATTTTTTCCAGAAATTCTTTTATGAAAATATCACAATACTTTTGATGTGTGCAAACATGAACCTGGATTTTTACACCTCTTGCGGTAACACTCGGTTTTCAACTAACTCACATCCAGATATTCCTGCAATCAATCCTGGGTGCCTTGAAGCCAAG... | TGGAAGAAATCCAATAGACATTAGCTTTCTGGAGTTGCAAAAGTTCTTTTCATCATTAACAGTACTCGTTCTATTTCCTGTGGTGCTTTCTTAAGAAAGGCTTTATTCAGAAGAAAATGACTTACTGATAGCATTTAAAGTTGCATCTACCATTGGTTAATACTCATTTTTTCCAGAAATTCTTTTATGAAAATATCACAATACTTTTGATGTGTGCAAACATGAACCTGGATTTTTACACCTCTTGCGGTAACACTCGGTTTTCAACTAACTCACATCCAGATATTCCTGCAATCAATCCTGGGTGCCTTGAAGCCAAG... |
Task1_train_41486 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CAGCCTCTCACTCAGATGTTCTGGGCGTTGCTCTCTTCATGCCTTTCTCCCCGCAGTTCTACAGCACCAAGGGCTCCTCTTTTCCCTCCAGCTGCTCACTTCCCACCAGTCTTTCCTCCCCTGCCCCTTAACCAACCTATTGGTGCCATGTGTCCTCTCTGCCACATTCATGGCTGGTAAAAATATTTCTTTTTCCCCAAATCTCCCTCGGACAACAGATCATACTCCTCCCTGCAGAGCCCCTTCAGATTCCATTCATCAGACCTGCTATTCAGGGAACAGAAATTCCTTTGGAAACTTCACACCTTTCTTTATGCCCT... | CAGCCTCTCACTCAGATGTTCTGGGCGTTGCTCTCTTCATGCCTTTCTCCCCGCAGTTCTACAGCACCAAGGGCTCCTCTTTTCCCTCCAGCTGCTCACTTCCCACCAGTCTTTCCTCCCCTGCCCCTTAACCAACCTATTGGTGCCATGTGTCCTCTCTGCCACATTCATGGCTGGTAAAAATATTTCTTTTTCCCCAAATCTCCCTCGGACAACAGATCATACTCCTCCCTGCAGAGCCCCTTCAGATTCCATTCATCAGACCTGCTATTCAGGGAACAGAAATTCCTTTGGAAACTTCACACCTTTCTTTATGCCCT... |
Task1_train_41487 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GTTTAAGTAAATGGAAGACAATTTTATTCTTACTTAAATTTCTTTGCTTCTTTCACAGAATTTTGAAAACCAACCTGGACAAGGTTCAGATGCCAGTAACTTCTTACAGCAATGCTCTGACCACAAAAGAAAAGCCAAAGCACTAGTGGCTTGCCAGATTGTTCTACCAGACCCAGGTATTGCAGGCTTTACTGTCATTGACTACTTCCATCAACTTTTGCAGACTTTTAATTTCAGGAAACTTCAGTGTGACTCTCAGGCACCTAACAATCACTTACTTGCTTTAGATCACTCAAATAGTGATCTCAGCAGCATATATA... | GTTTAAGTAAATGGAAGACAATTTTATTCTTACTTAAATTTCTTTGCTTCTTTCACAGAATTTTGAAAACCAACCTGGACAAGGTTCAGATGCCAGTAACTTCTTACAGCAATGCTCTGACCACAAAAGAAAAGCCAAAGCACTAGTGGCTTGCCAGATTGTTCTACCAGACCCAGGTATTGCAGGCTTTACTGTCATTGACTACTTCCATCAACTTTTGCAGACTTTTAATTTCAGGAAACTTCAGTGTGACTCTCAGGCACCTAACAATCACTTACTTGCTTTAGATCACTCAAATAGTGATCTCAGCAGCATATATA... |
Task1_train_41488 | Chromosome 11 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CACTAGTGGCTTGCCAGATTGTTCTACCAGACCCAGGTATTGCAGGCTTTACTGTCATTGACTACTTCCATCAACTTTTGCAGACTTTTAATTTCAGGAAACTTCAGTGTGACTCTCAGGCACCTAACAATCACTTACTTGCTTTAGATCACTCAAATAGTGATCTCAGCAGCATATATACTTCTGACAGCACTTCTGATTTTTTCAAGTCCTGCAGCAAGGATACTTTTTCAAAATTCTGGCAGCCATCACTTGAATTCACTTGCATTGTTTCACAACTAACAGATAATGATGATTTTTCAGCTTCAGAACAAAGTAAG... | CACTAGTGGCTTGCCAGATTGTTCTACCAGACCCAGGTATTGCAGGCTTTACTGTCATTGACTACTTCCATCAACTTTTGCAGACTTTTAATTTCAGGAAACTTCAGTGTGACTCTCAGGCACCTAACAATCACTTACTTGCTTTAGATCACTCAAATAGTGATCTCAGCAGCATATATACTTCTGACAGCACTTCTGATTTTTTCAAGTCCTGCAGCAAGGATACTTTTTCAAAATTCTGGCAGCCATCACTTGAATTCACTTGCATTGTTTCACAACTAACAGATAATGATGATTTTTCAGCTTCAGAACAAAGTAAG... |
Task1_train_41489 | Located on Chromosome 11, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | AGAAAACATGGCACATATACACCACGGAATACTATGCAGCCATAAAAAAGGATGAGTTCATGTCCTTTGCAGGGACATGGATGAAGCCAGAAACCATCATTTTCAGCAAACTATCACAAGGACAGAAAACCAAACACCGCATGTTCTCACTCATAGGTAGGAATTGAACAATGAGATCACTTGGATACAGAAACATCACACACTGGGGCCTGTCGGGTGGTGGTTGGGTGAGGGAGAGCATTAGGACCTAAGGTAAAATGATGAGTTGATGGGTGCAGCAAACCAACATGGTACATGTATACCTATGTATCAAACTTGCA... | AGAAAACATGGCACATATACACCACGGAATACTATGCAGCCATAAAAAAGGATGAGTTCATGTCCTTTGCAGGGACATGGATGAAGCCAGAAACCATCATTTTCAGCAAACTATCACAAGGACAGAAAACCAAACACCGCATGTTCTCACTCATAGGTAGGAATTGAACAATGAGATCACTTGGATACAGAAACATCACACACTGGGGCCTGTCGGGTGGTGGTTGGGTGAGGGAGAGCATTAGGACCTAAGGTAAAATGATGAGTTGATGGGTGCAGCAAACCAACATGGTACATGTATACCTATGTATCAAACTTGCA... |
Task1_train_41490 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TAGCCAAGGCTGGAGCCAGAGAAATGTACCTGGCCAGGCAATGCCCTTAGGTGGCATCAGGTGAGTCATCTGGCCAAAGTCATACTCTAGAAAGGGAAGATTGTGCATATAATTGAAAATGAGAGGGAGAAAGTGGCAACAAAACACCACAGCACAAGGTATCTGAGGGAAGGAAAGTTCCGGCCTTGTATTTTGTCCCTAGCATTTAGCCACCACTGTGGTAAGATATTGCTCCCGAATGGGAAATTTGTGTCCATCTGTGGCACATCTTTGCGACAAATCTTACCAGACTTCTATAAAGGTTGCCAATTAAGGAAGAA... | TAGCCAAGGCTGGAGCCAGAGAAATGTACCTGGCCAGGCAATGCCCTTAGGTGGCATCAGGTGAGTCATCTGGCCAAAGTCATACTCTAGAAAGGGAAGATTGTGCATATAATTGAAAATGAGAGGGAGAAAGTGGCAACAAAACACCACAGCACAAGGTATCTGAGGGAAGGAAAGTTCCGGCCTTGTATTTTGTCCCTAGCATTTAGCCACCACTGTGGTAAGATATTGCTCCCGAATGGGAAATTTGTGTCCATCTGTGGCACATCTTTGCGACAAATCTTACCAGACTTCTATAAAGGTTGCCAATTAAGGAAGAA... |
Task1_train_41491 | Here is a genetic alteration on Chromosome 11. Based on the data, is it a benign variant or a cause of disease? | Benign | GCCCTTAGGTGGCATCAGGTGAGTCATCTGGCCAAAGTCATACTCTAGAAAGGGAAGATTGTGCATATAATTGAAAATGAGAGGGAGAAAGTGGCAACAAAACACCACAGCACAAGGTATCTGAGGGAAGGAAAGTTCCGGCCTTGTATTTTGTCCCTAGCATTTAGCCACCACTGTGGTAAGATATTGCTCCCGAATGGGAAATTTGTGTCCATCTGTGGCACATCTTTGCGACAAATCTTACCAGACTTCTATAAAGGTTGCCAATTAAGGAAGAAATTCTAAATATTTCCAGGAGGAAAACTAGCTTAAATGTATTA... | GCCCTTAGGTGGCATCAGGTGAGTCATCTGGCCAAAGTCATACTCTAGAAAGGGAAGATTGTGCATATAATTGAAAATGAGAGGGAGAAAGTGGCAACAAAACACCACAGCACAAGGTATCTGAGGGAAGGAAAGTTCCGGCCTTGTATTTTGTCCCTAGCATTTAGCCACCACTGTGGTAAGATATTGCTCCCGAATGGGAAATTTGTGTCCATCTGTGGCACATCTTTGCGACAAATCTTACCAGACTTCTATAAAGGTTGCCAATTAAGGAAGAAATTCTAAATATTTCCAGGAGGAAAACTAGCTTAAATGTATTA... |
Task1_train_41492 | This sequence change occurs on Chromosome 11. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | ACAGCACAAGGTATCTGAGGGAAGGAAAGTTCCGGCCTTGTATTTTGTCCCTAGCATTTAGCCACCACTGTGGTAAGATATTGCTCCCGAATGGGAAATTTGTGTCCATCTGTGGCACATCTTTGCGACAAATCTTACCAGACTTCTATAAAGGTTGCCAATTAAGGAAGAAATTCTAAATATTTCCAGGAGGAAAACTAGCTTAAATGTATTAAAGGTACTTTCCAAACCCAAAAAGTCATTTAAAAAGTATTTTTTGAAACCTAAAAGTTCTATAGGTAGATTAAAGAGAAGTCAACTCAGACTCTGAAACAGCCTTA... | ACAGCACAAGGTATCTGAGGGAAGGAAAGTTCCGGCCTTGTATTTTGTCCCTAGCATTTAGCCACCACTGTGGTAAGATATTGCTCCCGAATGGGAAATTTGTGTCCATCTGTGGCACATCTTTGCGACAAATCTTACCAGACTTCTATAAAGGTTGCCAATTAAGGAAGAAATTCTAAATATTTCCAGGAGGAAAACTAGCTTAAATGTATTAAAGGTACTTTCCAAACCCAAAAAGTCATTTAAAAAGTATTTTTTGAAACCTAAAAGTTCTATAGGTAGATTAAAGAGAAGTCAACTCAGACTCTGAAACAGCCTTA... |
Task1_train_41493 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | ATATGGCTTAGCCTTGGAAATCATACATTGTCACTTCCATCATATTCTACTGGTTGATGTAGTTACAAAGTTCCATCCAAGGGGAAGGAACATAGCTCCTACATCTTGATGGAGGAAGGTCAGTATCACATTGTAAGAGAAGCACTTGGGATAGGATATGAATTAGGCTATCTTTGGAAAGTACAGATTGCACATATACCATTCATTAAAACCTGGAGTATTAAGCCTTTTAATTTTGAAACTTCTTTCTAGTACATTCCAGTTACTCCCACAGCCATCCCTTGTTATTTTCCCTCTTGATACTTTAAAAGTTCTCCTAG... | ATATGGCTTAGCCTTGGAAATCATACATTGTCACTTCCATCATATTCTACTGGTTGATGTAGTTACAAAGTTCCATCCAAGGGGAAGGAACATAGCTCCTACATCTTGATGGAGGAAGGTCAGTATCACATTGTAAGAGAAGCACTTGGGATAGGATATGAATTAGGCTATCTTTGGAAAGTACAGATTGCACATATACCATTCATTAAAACCTGGAGTATTAAGCCTTTTAATTTTGAAACTTCTTTCTAGTACATTCCAGTTACTCCCACAGCCATCCCTTGTTATTTTCCCTCTTGATACTTTAAAAGTTCTCCTAG... |
Task1_train_41494 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TTAACCTAGACCAGAGATCTGGAAAGACTTTCTGACATACAAGAGTTAGGTAAAGAAATCAAGGGAGGAAGAGCATTCCAGGCAGGGAAACAGGGAAGGAAGGAGAGAGCGAGCGAGCATGGGGCTTCTGAAATTTAGGCATGATCTTTCTCTCTCTTTATATATAAGCTCCAGATTATATTTATTACTGCTGTGTATCTCTTCTTTGATATATCTATACACATCTTAAATTTAAAAAGACCTAAACAGAACTTTTGATTCCCTCCTTAACCTGTTCCTTTCTGTCTTCTCATGTTAGTAAGTGGCATCACCAACCAGCC... | TTAACCTAGACCAGAGATCTGGAAAGACTTTCTGACATACAAGAGTTAGGTAAAGAAATCAAGGGAGGAAGAGCATTCCAGGCAGGGAAACAGGGAAGGAAGGAGAGAGCGAGCGAGCATGGGGCTTCTGAAATTTAGGCATGATCTTTCTCTCTCTTTATATATAAGCTCCAGATTATATTTATTACTGCTGTGTATCTCTTCTTTGATATATCTATACACATCTTAAATTTAAAAAGACCTAAACAGAACTTTTGATTCCCTCCTTAACCTGTTCCTTTCTGTCTTCTCATGTTAGTAAGTGGCATCACCAACCAGCC... |
Task1_train_41495 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | TGTTGGGTAGGAGTACAGATGCATTTGGAAACTCTGAGAGCGTTTCCTGCTGAGCCCCATGCTTTGGTTTGAGCTGTCAGATGTTTTGGGGCCCATCTTCTTGACTACATTTCCTGGCAGAACCTATGGTGGGACATAAGTGTGAGAGTGGGGTGTGTGTGTGTGTGCATGTTTCTTTAACCCAAACCACATATGGAGAATCCATAAAGAATTTATTTGAGCTGTTAGGATTATGGCTTCCTGGGCCAGGACAGAAAGGCTTTTGGGCAATGCCTGAGTCTCACCAAGACCCTTTGGCCCAAGGCATCCAGCACCAAGCT... | TGTTGGGTAGGAGTACAGATGCATTTGGAAACTCTGAGAGCGTTTCCTGCTGAGCCCCATGCTTTGGTTTGAGCTGTCAGATGTTTTGGGGCCCATCTTCTTGACTACATTTCCTGGCAGAACCTATGGTGGGACATAAGTGTGAGAGTGGGGTGTGTGTGTGTGTGCATGTTTCTTTAACCCAAACCACATATGGAGAATCCATAAAGAATTTATTTGAGCTGTTAGGATTATGGCTTCCTGGGCCAGGACAGAAAGGCTTTTGGGCAATGCCTGAGTCTCACCAAGACCCTTTGGCCCAAGGCATCCAGCACCAAGCT... |
Task1_train_41496 | A mutation has occurred on Chromosome 11. What is the medical relevance of this mutation? | Benign | AGCCAGTGTGAGACTCTGAAGGTGCGCTAGCCTTATTCATCATAGTTTAAAACATAGTTAGAAATATATGTAGCTTAGTGTTTAAGAAGCCAAACTTTAGGCCAGACAATTCTGGGTTCAAATAATTACTGATAATTTATTGGTTGTGGACAAGATACTTAACCATGCCAACTCTCGTGGGAATTGTGACACCTATAGTATTGTTGTGAGGATTACATGAATTAATTATATTTGTAAAAGGCTCAGTTGGCACTGTGCCTGTCGTATAAGATATGCTCAGAAAATTCTAGCTATTACTATGTTCATTCATTCATTCATTC... | AGCCAGTGTGAGACTCTGAAGGTGCGCTAGCCTTATTCATCATAGTTTAAAACATAGTTAGAAATATATGTAGCTTAGTGTTTAAGAAGCCAAACTTTAGGCCAGACAATTCTGGGTTCAAATAATTACTGATAATTTATTGGTTGTGGACAAGATACTTAACCATGCCAACTCTCGTGGGAATTGTGACACCTATAGTATTGTTGTGAGGATTACATGAATTAATTATATTTGTAAAAGGCTCAGTTGGCACTGTGCCTGTCGTATAAGATATGCTCAGAAAATTCTAGCTATTACTATGTTCATTCATTCATTCATTC... |
Task1_train_41497 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CATTTATATAGGCTTAAAAAAATGGTAGCTAGTGTGATAATAATCCTTGCAGATCTCCTAGAGAACAGGCATGATCACCTTCAGCTAGCACTGTTGGTTGCTCACCTGTCATCTATTGGGAGAAAGCATTCTCCCTGTTTACAAGTAAGGAAACCAAAACAAGGAGGTTAGAGAACTTACCTAAGATTGCCTACTACATGCAGAGTAAAGTAAGGATCCAGATGGAGGCAGTTCAACTCTGGAATTTGGGCTATTAATCACTGTACCCTTCCATCTCTTCTGTTTATGTGAGGAGACTGAAATCTACAGACATAGAACTT... | CATTTATATAGGCTTAAAAAAATGGTAGCTAGTGTGATAATAATCCTTGCAGATCTCCTAGAGAACAGGCATGATCACCTTCAGCTAGCACTGTTGGTTGCTCACCTGTCATCTATTGGGAGAAAGCATTCTCCCTGTTTACAAGTAAGGAAACCAAAACAAGGAGGTTAGAGAACTTACCTAAGATTGCCTACTACATGCAGAGTAAAGTAAGGATCCAGATGGAGGCAGTTCAACTCTGGAATTTGGGCTATTAATCACTGTACCCTTCCATCTCTTCTGTTTATGTGAGGAGACTGAAATCTACAGACATAGAACTT... |
Task1_train_41498 | Here is a genetic alteration on Chromosome 11. Based on the data, is it a benign variant or a cause of disease? | Benign | TTGGGAGAAAGCATTCTCCCTGTTTACAAGTAAGGAAACCAAAACAAGGAGGTTAGAGAACTTACCTAAGATTGCCTACTACATGCAGAGTAAAGTAAGGATCCAGATGGAGGCAGTTCAACTCTGGAATTTGGGCTATTAATCACTGTACCCTTCCATCTCTTCTGTTTATGTGAGGAGACTGAAATCTACAGACATAGAACTTCTCTGCTGTCATGCTGTTACCTGGATTGTACACAGAAGTCCAAATTACAGCTACATCCCCGTTTAAACAGTAAGCCGTTTCTAAATCTGAATCCTGAGGACTTTCGAGCAGCCAG... | TTGGGAGAAAGCATTCTCCCTGTTTACAAGTAAGGAAACCAAAACAAGGAGGTTAGAGAACTTACCTAAGATTGCCTACTACATGCAGAGTAAAGTAAGGATCCAGATGGAGGCAGTTCAACTCTGGAATTTGGGCTATTAATCACTGTACCCTTCCATCTCTTCTGTTTATGTGAGGAGACTGAAATCTACAGACATAGAACTTCTCTGCTGTCATGCTGTTACCTGGATTGTACACAGAAGTCCAAATTACAGCTACATCCCCGTTTAAACAGTAAGCCGTTTCTAAATCTGAATCCTGAGGACTTTCGAGCAGCCAG... |
Task1_train_41499 | This sequence change occurs on Chromosome 11. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TAGTCACTGTATTTGATGAAATCTGCAACATGGATGATATAAATGATCTTTCTGTCATACAGAAACAGGAAAAGCAGACTTCGACAGTAGATAAATCCAAGTTGAAATGTAGTCTATCTTAAGTTCTTATTCTGGGCAATCCCTCATAATCTCTGAAAACTTAGGGCCTCTTCAAATCATTGCTTGTCCTCAAGCAAACATGTTGTATAATCTGACTTCCATGCCAGTTAGGTTCACACCAGTATTTAGCCATTTAATATTTCCTAAAGTATTTAATGAATGACACCAGCAATGAATTTACTTAAGAGCCAGTCAGGGCC... | TAGTCACTGTATTTGATGAAATCTGCAACATGGATGATATAAATGATCTTTCTGTCATACAGAAACAGGAAAAGCAGACTTCGACAGTAGATAAATCCAAGTTGAAATGTAGTCTATCTTAAGTTCTTATTCTGGGCAATCCCTCATAATCTCTGAAAACTTAGGGCCTCTTCAAATCATTGCTTGTCCTCAAGCAAACATGTTGTATAATCTGACTTCCATGCCAGTTAGGTTCACACCAGTATTTAGCCATTTAATATTTCCTAAAGTATTTAATGAATGACACCAGCAATGAATTTACTTAAGAGCCAGTCAGGGCC... |
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