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_44900 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | AGATGGAAGTTCCAAGCCGCAGGGTCAGGGTGTAGAGTAGGCCCTTGAGGACTGGCAGCTAGGCTTGCTCAGCAGTTCAGCAGAATGCTCAAGAAGATGCCGGGCAGGCCCCGCTGGGGCTCCAGCCCTTGTGTTTCCAACGTGGGCATGGAGAGGGACCATTCTGAAGAGGAAGGAACTCCATAGTGGAGGGTGCTGAGCTCAGCCCTGGGAGTGCAGCTTGGTGGGAATGCAGGCTGCGCGCAGACCACTGTGGAGCCAGCCCAGTGCCGGGGAGCTGGCGTGTGAAGTGCTGAAGCCAGATTTGGAATTTTGGGGGT... | AGATGGAAGTTCCAAGCCGCAGGGTCAGGGTGTAGAGTAGGCCCTTGAGGACTGGCAGCTAGGCTTGCTCAGCAGTTCAGCAGAATGCTCAAGAAGATGCCGGGCAGGCCCCGCTGGGGCTCCAGCCCTTGTGTTTCCAACGTGGGCATGGAGAGGGACCATTCTGAAGAGGAAGGAACTCCATAGTGGAGGGTGCTGAGCTCAGCCCTGGGAGTGCAGCTTGGTGGGAATGCAGGCTGCGCGCAGACCACTGTGGAGCCAGCCCAGTGCCGGGGAGCTGGCGTGTGAAGTGCTGAAGCCAGATTTGGAATTTTGGGGGT... |
Task1_train_44901 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | CTTAGGGGCTGGCGGGGGTGCATTTTCAGGCAGCCTGTCTAAATAATCAATCCTAAGTCTCATGAATATCTCGAGAACCTGCCAAGGTCAGCCCAGACCAGGACTCAGAGGCAGCTAGCATACATCCGGGATTTGGGTCATTTGACTGGGCTGAGCCAGACCTCGCACAGCTTGGAAGCCTGGGAAGGTTTAGAAAGCACTTCTTCTTCTTCTTCTTTGTTTTTTTTTTTTTTCCATTTGAGACAGAGTCTTGCTGTGTTGCTAGGCTGGAGTGCAGTAGCACGATCTCGGCTCACTGCAACCTCGGCCTCCCGGGTTCA... | CTTAGGGGCTGGCGGGGGTGCATTTTCAGGCAGCCTGTCTAAATAATCAATCCTAAGTCTCATGAATATCTCGAGAACCTGCCAAGGTCAGCCCAGACCAGGACTCAGAGGCAGCTAGCATACATCCGGGATTTGGGTCATTTGACTGGGCTGAGCCAGACCTCGCACAGCTTGGAAGCCTGGGAAGGTTTAGAAAGCACTTCTTCTTCTTCTTCTTTGTTTTTTTTTTTTTTCCATTTGAGACAGAGTCTTGCTGTGTTGCTAGGCTGGAGTGCAGTAGCACGATCTCGGCTCACTGCAACCTCGGCCTCCCGGGTTCA... |
Task1_train_44902 | Given a variant located on Chromosome 17, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CACGCTGGCAGAACTATCTGAGAAGGCGTGGCCCGGGCGGGCCTGGGTTTGTGAAGAATGCACTGCCAGTCACACTCCCCACCCCTCCTGACTATCCACGCAGCGCCCCAGCTCCCAGGCCTTCACCTCCCCAGCACCTGAGCTCTGAAGGCAGGTCTACCAGGTGCCTGCCTGTCTCTCCCACGCCTGCCACCGCCTCCCTCCTGGGCCCTCTGCCTCCAGCACAGCCCCTCCCAAACCCTTCTCCACGCTGCCAGCCGTTTCTGAAAAGGCAAACCAGACTCAGACCCTTCCCCACGCCACTGCTCTTGCTGATAATG... | CACGCTGGCAGAACTATCTGAGAAGGCGTGGCCCGGGCGGGCCTGGGTTTGTGAAGAATGCACTGCCAGTCACACTCCCCACCCCTCCTGACTATCCACGCAGCGCCCCAGCTCCCAGGCCTTCACCTCCCCAGCACCTGAGCTCTGAAGGCAGGTCTACCAGGTGCCTGCCTGTCTCTCCCACGCCTGCCACCGCCTCCCTCCTGGGCCCTCTGCCTCCAGCACAGCCCCTCCCAAACCCTTCTCCACGCTGCCAGCCGTTTCTGAAAAGGCAAACCAGACTCAGACCCTTCCCCACGCCACTGCTCTTGCTGATAATG... |
Task1_train_44903 | Given a variant located on Chromosome 17, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AGCCCTGGCCTGGAGACCTGCTACCCCTGCCTTTCTCTTCGGTGACAAAAGGGCCTAGGGTGCTACCTTCCCAAGTAGGGCAGTGGAGGCCCACAAGGGGCCAGCCTTGACCAGGATAACAATGGCAAACGTTTTATATACTTGCCACGTGCCAGGCACAGTTCCAGAGCTGCACTGCCCAATACGGTAGCCACAGCCACACAGGGCTGCTGAGCGCCTGAAAGGTGGCTAATCTGAACAGGGGTGTGCCTAAGTGTAACATACACACTGGATTTTGGAGACACCTGACAAAAAGAGTGTAAGATATCTCAACACTTTTT... | AGCCCTGGCCTGGAGACCTGCTACCCCTGCCTTTCTCTTCGGTGACAAAAGGGCCTAGGGTGCTACCTTCCCAAGTAGGGCAGTGGAGGCCCACAAGGGGCCAGCCTTGACCAGGATAACAATGGCAAACGTTTTATATACTTGCCACGTGCCAGGCACAGTTCCAGAGCTGCACTGCCCAATACGGTAGCCACAGCCACACAGGGCTGCTGAGCGCCTGAAAGGTGGCTAATCTGAACAGGGGTGTGCCTAAGTGTAACATACACACTGGATTTTGGAGACACCTGACAAAAAGAGTGTAAGATATCTCAACACTTTTT... |
Task1_train_44904 | Chromosome 17 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CAGTGGTGTGATCCTAGCTCTCTGCAGCCTTGAACTCCTGAGCTCAAGCGAGCTTCCTGCCTCAGCCTCCCAAGCAGCTGGGACAACAGGCATGTGCCACCGCCCCTGGCAAATTTTTAAATTTTTAGTACAGATGAGATCTTGCTTTGTTGTCTAGGCTAGTTTCAAACTCCTGGCCTCGAGGTATCTTCCTGCCTTGACCACCCAAAGTGCTGAGATTACAGGTGTGAGGCACCACACCCTGCGGGTGCACACTCCATTGCTGCTGTGTCTGCTCTGCTCCTGCCCCCATGCTTCAGATAACTCTGCCTTCTGCCAGA... | CAGTGGTGTGATCCTAGCTCTCTGCAGCCTTGAACTCCTGAGCTCAAGCGAGCTTCCTGCCTCAGCCTCCCAAGCAGCTGGGACAACAGGCATGTGCCACCGCCCCTGGCAAATTTTTAAATTTTTAGTACAGATGAGATCTTGCTTTGTTGTCTAGGCTAGTTTCAAACTCCTGGCCTCGAGGTATCTTCCTGCCTTGACCACCCAAAGTGCTGAGATTACAGGTGTGAGGCACCACACCCTGCGGGTGCACACTCCATTGCTGCTGTGTCTGCTCTGCTCCTGCCCCCATGCTTCAGATAACTCTGCCTTCTGCCAGA... |
Task1_train_44905 | This sequence variant lies on Chromosome 17. Is it clinically significant, and what condition might it cause if any? | Benign | TTGGGGACAGGTGTGCAGAGCCAAAGGAGCAGTTGAGCGAGGAGGTGAGAAGGAGCACAGAGCCGCTGCTGTCCACGGCGGCCAGGGCACTGCTCTCGGGGCTCACAGCAGTCTGCAGGAACGGTGGGCAGGGGTCAGGGATGGGCGCCCCGGAGCGCAGGGCTGCCTCCAACAGTGCCAGCAGTTCTGGGCCAGCTGAGGGACTGGGGGTGGTGAACAGGATGCCCTGGGGCACAGGTAGCTGCTCTGCTGGTTCCAAAGTGGGCCTGGGCACAGCCGAGGGCACCTCCACCCCCAGGTCTCCCGCCAGTAGACTCAGT... | TTGGGGACAGGTGTGCAGAGCCAAAGGAGCAGTTGAGCGAGGAGGTGAGAAGGAGCACAGAGCCGCTGCTGTCCACGGCGGCCAGGGCACTGCTCTCGGGGCTCACAGCAGTCTGCAGGAACGGTGGGCAGGGGTCAGGGATGGGCGCCCCGGAGCGCAGGGCTGCCTCCAACAGTGCCAGCAGTTCTGGGCCAGCTGAGGGACTGGGGGTGGTGAACAGGATGCCCTGGGGCACAGGTAGCTGCTCTGCTGGTTCCAAAGTGGGCCTGGGCACAGCCGAGGGCACCTCCACCCCCAGGTCTCCCGCCAGTAGACTCAGT... |
Task1_train_44906 | The following genetic variant occurs on Chromosome 17. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GGGGCTCACAGCAGTCTGCAGGAACGGTGGGCAGGGGTCAGGGATGGGCGCCCCGGAGCGCAGGGCTGCCTCCAACAGTGCCAGCAGTTCTGGGCCAGCTGAGGGACTGGGGGTGGTGAACAGGATGCCCTGGGGCACAGGTAGCTGCTCTGCTGGTTCCAAAGTGGGCCTGGGCACAGCCGAGGGCACCTCCACCCCCAGGTCTCCCGCCAGTAGACTCAGTAGAGCATCCCCAGCAAGGTCTGAGGTGGGAGCGAGGGCTGCGCTGCGAAGCACAGCTGCCAGTTGTGGGTTGGTGGCTCGGGCCCCAGCGCCCAGGG... | GGGGCTCACAGCAGTCTGCAGGAACGGTGGGCAGGGGTCAGGGATGGGCGCCCCGGAGCGCAGGGCTGCCTCCAACAGTGCCAGCAGTTCTGGGCCAGCTGAGGGACTGGGGGTGGTGAACAGGATGCCCTGGGGCACAGGTAGCTGCTCTGCTGGTTCCAAAGTGGGCCTGGGCACAGCCGAGGGCACCTCCACCCCCAGGTCTCCCGCCAGTAGACTCAGTAGAGCATCCCCAGCAAGGTCTGAGGTGGGAGCGAGGGCTGCGCTGCGAAGCACAGCTGCCAGTTGTGGGTTGGTGGCTCGGGCCCCAGCGCCCAGGG... |
Task1_train_44907 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | CCTCATCCCAGGGCCCCTAAGCTGCTCTTCCTCTGCTGGGCTTCCAGGAGCCCAGTGCATGCCCCTGACTCCTGTTTTTCCATGTTCGTCCTTCTTTTCTCTTAAACTCCAGACTCAAAAATCCAGCTACCTCCTCAGCTCCCTGATGCTCCAGGTGCCCCAGGCCCTCAACATGTCCCAACTGAAACCCTCATTTAGCCCCTAAACCTGCCCTGACCCACCAAGTCTGGGCTTGGGAGAGGCTTGGCACCCTTCCTCTTCCATGTCCACCCAGTCTCCCAGCCAGATCCCTTTTCCCCAAAGCTCCGAGTCCTTCTTGC... | CCTCATCCCAGGGCCCCTAAGCTGCTCTTCCTCTGCTGGGCTTCCAGGAGCCCAGTGCATGCCCCTGACTCCTGTTTTTCCATGTTCGTCCTTCTTTTCTCTTAAACTCCAGACTCAAAAATCCAGCTACCTCCTCAGCTCCCTGATGCTCCAGGTGCCCCAGGCCCTCAACATGTCCCAACTGAAACCCTCATTTAGCCCCTAAACCTGCCCTGACCCACCAAGTCTGGGCTTGGGAGAGGCTTGGCACCCTTCCTCTTCCATGTCCACCCAGTCTCCCAGCCAGATCCCTTTTCCCCAAAGCTCCGAGTCCTTCTTGC... |
Task1_train_44908 | 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 | CAGATGAATATGCAAAAACTGATCATACTGGCTGCTCTGGCAGAAAATCTCATGGCTAAAGAGGACTTTTCAACAAACCTTTTGTACCTCTTGAGTTTTGAACCATGTGGATGTTTTCCCGATCCAGAACACCATTCAAATGAGAAAAAATTCTGTTCTAGCCTCTTCCCCAAAATCAATGTCAACTTCACCTATCTAGTTTCCAGAAATCAGGTTCTTTCCCTTTCTGAAAAACCACTATTGCACTTTTCACACTACACCCTTGTCCTTGCAGTGATCCTTAAACCTTCCAGGGCCTTCTCCACCTAGAAGAAATTCCT... | CAGATGAATATGCAAAAACTGATCATACTGGCTGCTCTGGCAGAAAATCTCATGGCTAAAGAGGACTTTTCAACAAACCTTTTGTACCTCTTGAGTTTTGAACCATGTGGATGTTTTCCCGATCCAGAACACCATTCAAATGAGAAAAAATTCTGTTCTAGCCTCTTCCCCAAAATCAATGTCAACTTCACCTATCTAGTTTCCAGAAATCAGGTTCTTTCCCTTTCTGAAAAACCACTATTGCACTTTTCACACTACACCCTTGTCCTTGCAGTGATCCTTAAACCTTCCAGGGCCTTCTCCACCTAGAAGAAATTCCT... |
Task1_train_44909 | A genetic alteration is present on Chromosome 17. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | ACCATCACCTGTGCCATGGGACAGAACCTGGGAACATGTAGGGTGGGGAGTATGAGCACCAACATACCCTGCTGGTCAAAGTACCCTAGGACAAAGGGGCAAATGGTGGGCATGGAAAAACTGAAGCCCGAGCCTGCCCACAGCTATGCTTTGGCCTCTCCAGCAGGGTGCTCCTGCTCTGCACTCCAGAAACACCCTGACAGGCTCAGAGAGGAGATGGAAACTGACATACCCAACCCACTTCCTCAAACACTTCATGCTGCTGCCCCAGCCTTCCCGCAGACTTGGCCTAATGAAAATACATACTTCTTCATTCGGAG... | ACCATCACCTGTGCCATGGGACAGAACCTGGGAACATGTAGGGTGGGGAGTATGAGCACCAACATACCCTGCTGGTCAAAGTACCCTAGGACAAAGGGGCAAATGGTGGGCATGGAAAAACTGAAGCCCGAGCCTGCCCACAGCTATGCTTTGGCCTCTCCAGCAGGGTGCTCCTGCTCTGCACTCCAGAAACACCCTGACAGGCTCAGAGAGGAGATGGAAACTGACATACCCAACCCACTTCCTCAAACACTTCATGCTGCTGCCCCAGCCTTCCCGCAGACTTGGCCTAATGAAAATACATACTTCTTCATTCGGAG... |
Task1_train_44910 | This variant lies on Chromosome 17. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TGCTCTGCACTCCAGAAACACCCTGACAGGCTCAGAGAGGAGATGGAAACTGACATACCCAACCCACTTCCTCAAACACTTCATGCTGCTGCCCCAGCCTTCCCGCAGACTTGGCCTAATGAAAATACATACTTCTTCATTCGGAGAGACAAAACAAGAACTAGAGTTTTAATGATAATAAAAGCAATAATAATAAAAGCAATAACAATAAAAACAAGATCAGACTCTCACTGGGGTAGGCAAGGGACTGAGGAGGTGAAACCAACCCGTATGGTGTCCCAGCACGGCACCTGCTAAGGAGGGAGGGTGGGAAAGCCCAG... | TGCTCTGCACTCCAGAAACACCCTGACAGGCTCAGAGAGGAGATGGAAACTGACATACCCAACCCACTTCCTCAAACACTTCATGCTGCTGCCCCAGCCTTCCCGCAGACTTGGCCTAATGAAAATACATACTTCTTCATTCGGAGAGACAAAACAAGAACTAGAGTTTTAATGATAATAAAAGCAATAATAATAAAAGCAATAACAATAAAAACAAGATCAGACTCTCACTGGGGTAGGCAAGGGACTGAGGAGGTGAAACCAACCCGTATGGTGTCCCAGCACGGCACCTGCTAAGGAGGGAGGGTGGGAAAGCCCAG... |
Task1_train_44911 | Chromosome 17 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GGAAAAGACACTGTAACCTCTTAAGCTCTAGAAAATGGAACTGTAAAGCCATTGTGGCCTTGTCACCTCCTAATTTGATAGAATTTTTTTTTTTTGCTTTTTTTGACAGGGTCTCACTTTGTCACTCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCATTGCAGCCTCCACCTCCTGGGCTAAAGCAATCCTCCTGCCTCTGCCTCCTGAGTAGCTGGGACTACAGGCGCACACCACCATACCCCTGCTAATTTTTGTACTTTTTGTAGAGAGGGGATTTCACCATGTTGCCCAGGCTGGTCTCCAACTGCTGAGCTTA... | GGAAAAGACACTGTAACCTCTTAAGCTCTAGAAAATGGAACTGTAAAGCCATTGTGGCCTTGTCACCTCCTAATTTGATAGAATTTTTTTTTTTTGCTTTTTTTGACAGGGTCTCACTTTGTCACTCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCATTGCAGCCTCCACCTCCTGGGCTAAAGCAATCCTCCTGCCTCTGCCTCCTGAGTAGCTGGGACTACAGGCGCACACCACCATACCCCTGCTAATTTTTGTACTTTTTGTAGAGAGGGGATTTCACCATGTTGCCCAGGCTGGTCTCCAACTGCTGAGCTTA... |
Task1_train_44912 | Consider a variant on Chromosome 17. Determine its clinical classification and disease relevance. | Benign | ACTTTTTGTAGAGAGGGGATTTCACCATGTTGCCCAGGCTGGTCTCCAACTGCTGAGCTTAAACAATCCACCCACCTCAGCCTCCCAGAGTGCTGAGATTACAGCTGTGAGCCACCACATCTGGCCATAATTTGGTAGAATTTTCTTAATCTTAGGTCACTGGTTCAGAAAGGAGACAACCTAGGCACCTAATGGGGGCAGGGTGTCTGCAGACTCTCTCAGAAAGCCAGACTTCCTGGGCCCGCACGATGGTGCAAGCCGGTAATCCCAAAACTTTGGAAGGCTGAAGCCAGTGGATCACTTGAGGTCAGGAGTTTGAG... | ACTTTTTGTAGAGAGGGGATTTCACCATGTTGCCCAGGCTGGTCTCCAACTGCTGAGCTTAAACAATCCACCCACCTCAGCCTCCCAGAGTGCTGAGATTACAGCTGTGAGCCACCACATCTGGCCATAATTTGGTAGAATTTTCTTAATCTTAGGTCACTGGTTCAGAAAGGAGACAACCTAGGCACCTAATGGGGGCAGGGTGTCTGCAGACTCTCTCAGAAAGCCAGACTTCCTGGGCCCGCACGATGGTGCAAGCCGGTAATCCCAAAACTTTGGAAGGCTGAAGCCAGTGGATCACTTGAGGTCAGGAGTTTGAG... |
Task1_train_44913 | 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 | GTATTTTTAGTAGAGACCGGGTTTCACCGTGTTGGCCAGGATGGTCTCTATCTCTTGACCTTGTGATCCGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGCCCGGTCCAACAGGAATAACTCTAAGAAGTTTGGGGACAGGAGACTAAGAACCCCTAAGAAAAGATCATGCTGTTTCTTCCATTGCTTTCTGTATCCTTATATCCTTTCCTGGAATGCCTTTCCCCCTGTGACCACCAGATGGACTCCTAATTTGCAAAACAAAAAGCGAGAAAATCTGGCTAAGTATGTTTTTTGTTTGT... | GTATTTTTAGTAGAGACCGGGTTTCACCGTGTTGGCCAGGATGGTCTCTATCTCTTGACCTTGTGATCCGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGCCCGGTCCAACAGGAATAACTCTAAGAAGTTTGGGGACAGGAGACTAAGAACCCCTAAGAAAAGATCATGCTGTTTCTTCCATTGCTTTCTGTATCCTTATATCCTTTCCTGGAATGCCTTTCCCCCTGTGACCACCAGATGGACTCCTAATTTGCAAAACAAAAAGCGAGAAAATCTGGCTAAGTATGTTTTTTGTTTGT... |
Task1_train_44914 | Given this context: Chromosome 17 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TTCTCCTGCCTCAGCCTACCAGTGTGCTGGGATTACAGGCATGAGCCACTGTGCCCATCCTTTTTTTATTTTATTTAGTTATTTATTTTATTTTTTTTGAGATGGAGTCTCACTCTGTTGCCCGGGCTGGAGTGCAGTAGCCTGGTCTTGGCTCACTGCAACCTCCGCCTCCCGGGTTCTGGCGATTCTCTTGTCTCAGCCTCCCAAGTAGGTGGGATTATAGGCGGGCACCACTGTGCCTGGCTAGTTTTTGTATTTTTAGTAGAGATGGGGTTTTGCCAAGTTGACCAGGCTGGTCTTGAACTCCTGACCTCAGGTGA... | TTCTCCTGCCTCAGCCTACCAGTGTGCTGGGATTACAGGCATGAGCCACTGTGCCCATCCTTTTTTTATTTTATTTAGTTATTTATTTTATTTTTTTTGAGATGGAGTCTCACTCTGTTGCCCGGGCTGGAGTGCAGTAGCCTGGTCTTGGCTCACTGCAACCTCCGCCTCCCGGGTTCTGGCGATTCTCTTGTCTCAGCCTCCCAAGTAGGTGGGATTATAGGCGGGCACCACTGTGCCTGGCTAGTTTTTGTATTTTTAGTAGAGATGGGGTTTTGCCAAGTTGACCAGGCTGGTCTTGAACTCCTGACCTCAGGTGA... |
Task1_train_44915 | Given this variant on Chromosome 17, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GGGCGGGGACGGAACGGGCTCGGGCTGCGGGGCCTCCAGACTCAGTCGCACGCTCAGATTTCGGGATTTCTACCCCCGGCTGGGATCGCGTAACTTCCTCATTCCCGCCTGGACCCCTGCCCCCGGCCCGCCTGGCCTGGCGTGAGCCCCGTAGCCGCGCGCTCTCCGGACCACCCAGGGCCGCTTCCCCGCGCAGCTGCTGCGCCGCCCCAGGTCGGAGCCTTCCGGGCCTGGCTGGGTGTTCCCCGGGGCTCTGGTTACGGGACGGGGCGGGGGGCGGGGGGCGGGACTGGGATTGTGGATGAAGGACTAAGGTAGGG... | GGGCGGGGACGGAACGGGCTCGGGCTGCGGGGCCTCCAGACTCAGTCGCACGCTCAGATTTCGGGATTTCTACCCCCGGCTGGGATCGCGTAACTTCCTCATTCCCGCCTGGACCCCTGCCCCCGGCCCGCCTGGCCTGGCGTGAGCCCCGTAGCCGCGCGCTCTCCGGACCACCCAGGGCCGCTTCCCCGCGCAGCTGCTGCGCCGCCCCAGGTCGGAGCCTTCCGGGCCTGGCTGGGTGTTCCCCGGGGCTCTGGTTACGGGACGGGGCGGGGGGCGGGGGGCGGGACTGGGATTGTGGATGAAGGACTAAGGTAGGG... |
Task1_train_44916 | This variant lies on Chromosome 17. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ACAGAAAGGGTGATGGATGGAAGGATATGAGTTGGAAAGGTGGAGGGCTAGGAGGGTAGGCAGGTAGATGGATGAATGATAGACGGTACATAAAGGGATGAGTAAATGCTTGGGAAGATGGATGGATGGATGATGAAGGGTGGGTGGATAGATGTGTGGATGGGTGAGTGGGTGAGCACACAGATGACATTTAGTCTAAGTCTGTGGCAAGCAGCAAAGCAGGGCATATGTGGCAGAGCCTCTAGGATCTCCAGACAAGCTGGAGGGACACACGTGGAAAAGGTTTGGGAGTGTGGAAAGGGGCTACTCTGGGAGAGGCA... | ACAGAAAGGGTGATGGATGGAAGGATATGAGTTGGAAAGGTGGAGGGCTAGGAGGGTAGGCAGGTAGATGGATGAATGATAGACGGTACATAAAGGGATGAGTAAATGCTTGGGAAGATGGATGGATGGATGATGAAGGGTGGGTGGATAGATGTGTGGATGGGTGAGTGGGTGAGCACACAGATGACATTTAGTCTAAGTCTGTGGCAAGCAGCAAAGCAGGGCATATGTGGCAGAGCCTCTAGGATCTCCAGACAAGCTGGAGGGACACACGTGGAAAAGGTTTGGGAGTGTGGAAAGGGGCTACTCTGGGAGAGGCA... |
Task1_train_44917 | A mutation on Chromosome 17 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GACATCCCTTCACATCACAGGTAGAAGAGAGAACAAGGATGAACAAGCAGCAGAACTCTCCCTTGGCCAAGAGCAAGCCAGGCAGCACGGGGCCTGAGCCCCCCATCCCCCAGGCCTCCCCAGGGCCCCCAGGACCCCTTTCCCAGACTCCTCCTATGCAGAGGCCGGTGGAGCCCCAGGAGGGACCGCACAAGGTGAGTCTCTCCCCACCCCTGTCTTAATGAAGACACAGGGAGCTTTGTTCAGAGCACAGGTACACACACACGCGCGCACACACACACACACACACACACACCTGCTCAGCCGTGAGCCAGGATTAC... | GACATCCCTTCACATCACAGGTAGAAGAGAGAACAAGGATGAACAAGCAGCAGAACTCTCCCTTGGCCAAGAGCAAGCCAGGCAGCACGGGGCCTGAGCCCCCCATCCCCCAGGCCTCCCCAGGGCCCCCAGGACCCCTTTCCCAGACTCCTCCTATGCAGAGGCCGGTGGAGCCCCAGGAGGGACCGCACAAGGTGAGTCTCTCCCCACCCCTGTCTTAATGAAGACACAGGGAGCTTTGTTCAGAGCACAGGTACACACACACGCGCGCACACACACACACACACACACACACCTGCTCAGCCGTGAGCCAGGATTAC... |
Task1_train_44918 | A variant has been detected on Chromosome 17. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CATCACAGGTAGAAGAGAGAACAAGGATGAACAAGCAGCAGAACTCTCCCTTGGCCAAGAGCAAGCCAGGCAGCACGGGGCCTGAGCCCCCCATCCCCCAGGCCTCCCCAGGGCCCCCAGGACCCCTTTCCCAGACTCCTCCTATGCAGAGGCCGGTGGAGCCCCAGGAGGGACCGCACAAGGTGAGTCTCTCCCCACCCCTGTCTTAATGAAGACACAGGGAGCTTTGTTCAGAGCACAGGTACACACACACGCGCGCACACACACACACACACACACACACCTGCTCAGCCGTGAGCCAGGATTACAGAGCACAGGCT... | CATCACAGGTAGAAGAGAGAACAAGGATGAACAAGCAGCAGAACTCTCCCTTGGCCAAGAGCAAGCCAGGCAGCACGGGGCCTGAGCCCCCCATCCCCCAGGCCTCCCCAGGGCCCCCAGGACCCCTTTCCCAGACTCCTCCTATGCAGAGGCCGGTGGAGCCCCAGGAGGGACCGCACAAGGTGAGTCTCTCCCCACCCCTGTCTTAATGAAGACACAGGGAGCTTTGTTCAGAGCACAGGTACACACACACGCGCGCACACACACACACACACACACACACCTGCTCAGCCGTGAGCCAGGATTACAGAGCACAGGCT... |
Task1_train_44919 | A mutation is present on Chromosome 17. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TTGCCAGTTAGAACCGCAGCTCCACCATCATCCGGCTTCATAACCCTGGACGTATTCACTAACTCCCCTGAACCTCAGTTTTCTCATCCATCAAAGTGGGGGAGCTCACCTCTCAGAGGTGAGGCTTAAACATCTGAGAAGTGCCTGTCGCAGCGCCAGCTCGCAGCACGTGGACTTCTCTCCACAGGTGCCTCAGAGGACCTCATCTATCGCCACTGCCCTTAACACCAGTGGGGCCGGAGGGTCCCGGCCAGCCCAGGCAGTCCGTGCCAGGTAATGCCTGGGTAGGGCAACGCCTGGGTGAGGTCTGAGGGCAGCCT... | TTGCCAGTTAGAACCGCAGCTCCACCATCATCCGGCTTCATAACCCTGGACGTATTCACTAACTCCCCTGAACCTCAGTTTTCTCATCCATCAAAGTGGGGGAGCTCACCTCTCAGAGGTGAGGCTTAAACATCTGAGAAGTGCCTGTCGCAGCGCCAGCTCGCAGCACGTGGACTTCTCTCCACAGGTGCCTCAGAGGACCTCATCTATCGCCACTGCCCTTAACACCAGTGGGGCCGGAGGGTCCCGGCCAGCCCAGGCAGTCCGTGCCAGGTAATGCCTGGGTAGGGCAACGCCTGGGTGAGGTCTGAGGGCAGCCT... |
Task1_train_44920 | Chromosome 17 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AATGAACTGTGAGAAACTCTGAGGACTGTGGGACGTTAGTGCAGAAAAAGATCATGATTCTGAAACTTAGAATATGGAACCAGGGAGGAAGGGATGACATACTCCTCTAGAGATTTAGATGTCAGTGTTAATGGGGAAAGTAAACCCAGGAAATAAAGGGAGTCAGTGAGGTAAGTGAGGAGCCTTTGGATGCTCAGAACTCTCCTTCAGGAAAAGCAGAAGCGGAGAGGGGAAGGGAGGGGGGCGGGCGAGGCAAGAGAAGCAACTTTGCCCTTATTTGGTCAAAGGTTCTGCAGGAGCTGTTAGGGCCCGGACGCCTG... | AATGAACTGTGAGAAACTCTGAGGACTGTGGGACGTTAGTGCAGAAAAAGATCATGATTCTGAAACTTAGAATATGGAACCAGGGAGGAAGGGATGACATACTCCTCTAGAGATTTAGATGTCAGTGTTAATGGGGAAAGTAAACCCAGGAAATAAAGGGAGTCAGTGAGGTAAGTGAGGAGCCTTTGGATGCTCAGAACTCTCCTTCAGGAAAAGCAGAAGCGGAGAGGGGAAGGGAGGGGGGCGGGCGAGGCAAGAGAAGCAACTTTGCCCTTATTTGGTCAAAGGTTCTGCAGGAGCTGTTAGGGCCCGGACGCCTG... |
Task1_train_44921 | A mutation found on Chromosome 17 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TTGGCTTGGAGGAAGTGGGGGACATTTCTGCTTTTTTTCCTCCTGGGACTGGAGATGCTTGAAAAAGCTGGGGGAAGGGGCGGCTGGAGCAAGCAGATGGGACAAACTCTGGGAACACCGAAGGATCTAGGGAAAGGAGGCTGTGAGGAGGGCAGCAGGGATGGATAGAAAAGGGCAGCTAGAGCTGGAACCTGATAGGGAATTGGGGGCCCAAGGAGATTTCGGAGCAGGAAAATGAGAACCAGAAAGGATTTGAAGGCCACCAGCCATGGAGAACAGACTGCTTGACCAGAGGGGTGGAAGGAGAAGGCCTAAGTGGA... | TTGGCTTGGAGGAAGTGGGGGACATTTCTGCTTTTTTTCCTCCTGGGACTGGAGATGCTTGAAAAAGCTGGGGGAAGGGGCGGCTGGAGCAAGCAGATGGGACAAACTCTGGGAACACCGAAGGATCTAGGGAAAGGAGGCTGTGAGGAGGGCAGCAGGGATGGATAGAAAAGGGCAGCTAGAGCTGGAACCTGATAGGGAATTGGGGGCCCAAGGAGATTTCGGAGCAGGAAAATGAGAACCAGAAAGGATTTGAAGGCCACCAGCCATGGAGAACAGACTGCTTGACCAGAGGGGTGGAAGGAGAAGGCCTAAGTGGA... |
Task1_train_44922 | A variant was discovered on Chromosome 17. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CCCTTCCTCCCATCTTCCTTTGAAGAATCTGGAGGCTTTGTCCTGAGCTAGTCACCTGGGAGGGGTTGAGCTGGGGAAATGGTCCACATTCTCCAGGTAGCTGGCCAGCCAGGACATGGTCTCACTGAGCCCCACAGCCCCTGTCCGCTCCCGCATTGAGGCTCCAGCCTCGGGCAGCCCCACGAAGTCCTCTCGTTTAATCCGCTCCGGTGTGGCTTCGATGATCTGCTTGGCTAGTGAGATCATGTCCACCTGGAAGAAGGGAGAAGCTGAGTGAGTCCTTAGGGGCCCCAGCTGCCAGCTGTAACCTCAGTCCATTC... | CCCTTCCTCCCATCTTCCTTTGAAGAATCTGGAGGCTTTGTCCTGAGCTAGTCACCTGGGAGGGGTTGAGCTGGGGAAATGGTCCACATTCTCCAGGTAGCTGGCCAGCCAGGACATGGTCTCACTGAGCCCCACAGCCCCTGTCCGCTCCCGCATTGAGGCTCCAGCCTCGGGCAGCCCCACGAAGTCCTCTCGTTTAATCCGCTCCGGTGTGGCTTCGATGATCTGCTTGGCTAGTGAGATCATGTCCACCTGGAAGAAGGGAGAAGCTGAGTGAGTCCTTAGGGGCCCCAGCTGCCAGCTGTAACCTCAGTCCATTC... |
Task1_train_44923 | This variant lies on Chromosome 17. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TCTGGGCCAGACACCCAGATTCCCACCCTCAGGACAACCCACCCTCCGGCTGACAGCCCTCTCTACGTAGCTCCCTCTCCCCAAACGCCTCTGCCTCCCCTGGCCTCCAGGCCTAGCCTACCCCATCTACCGCTCTGGCTCCAGCCTGAGCCCCCCGCCCTCCTCGGGGAACAGATGGGAGCTGGCGGAGGCTCTCAGCACGGGCTCCGCCAGGTGTCCAGGATGGAGATGGGAGGAGGCCCGTCGGGCTCGGCTATGTGCAGTGAAGCTGGGGTTGGGGTAAGGACTCCGCCCCAGGGCGCAGGTGCGCAGTCCTGGCT... | TCTGGGCCAGACACCCAGATTCCCACCCTCAGGACAACCCACCCTCCGGCTGACAGCCCTCTCTACGTAGCTCCCTCTCCCCAAACGCCTCTGCCTCCCCTGGCCTCCAGGCCTAGCCTACCCCATCTACCGCTCTGGCTCCAGCCTGAGCCCCCCGCCCTCCTCGGGGAACAGATGGGAGCTGGCGGAGGCTCTCAGCACGGGCTCCGCCAGGTGTCCAGGATGGAGATGGGAGGAGGCCCGTCGGGCTCGGCTATGTGCAGTGAAGCTGGGGTTGGGGTAAGGACTCCGCCCCAGGGCGCAGGTGCGCAGTCCTGGCT... |
Task1_train_44924 | Given a variant located on Chromosome 17, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TTCCACTCTTGTCCGCCAGGAGGAGAAAAGGTTCCCTCGAAGGACGTCTTTGCTTGCGCGTTCACGGAGCCTTGAGAACGAGTGGCCGAGGGGACCCCTGCGGCCCTGCGCGCCTGTGAGTCTCCCGGGCGGGCGGGCGGTGGGGGTGCGAGGCCGGGGGGTGGGTGCGAGGCGTGGGGGAGGTGCGAGGCGGGCGGGGCGGGGGGCGCGAGGCGGGAGGGCGCACGCGCAGAAGGCTGGCTGGGGTGACGCGGCGCCGGGCTTGGGCTTCTGTATTCCGCGTGTCTGGAGGAAGGTCCGGAGGTGGGCGGGAGCCCTGC... | TTCCACTCTTGTCCGCCAGGAGGAGAAAAGGTTCCCTCGAAGGACGTCTTTGCTTGCGCGTTCACGGAGCCTTGAGAACGAGTGGCCGAGGGGACCCCTGCGGCCCTGCGCGCCTGTGAGTCTCCCGGGCGGGCGGGCGGTGGGGGTGCGAGGCCGGGGGGTGGGTGCGAGGCGTGGGGGAGGTGCGAGGCGGGCGGGGCGGGGGGCGCGAGGCGGGAGGGCGCACGCGCAGAAGGCTGGCTGGGGTGACGCGGCGCCGGGCTTGGGCTTCTGTATTCCGCGTGTCTGGAGGAAGGTCCGGAGGTGGGCGGGAGCCCTGC... |
Task1_train_44925 | A genomic variant on Chromosome 17 is under review. What is the biological outcome — benign or pathogenic? | Benign | AGAACGAGTGGCCGAGGGGACCCCTGCGGCCCTGCGCGCCTGTGAGTCTCCCGGGCGGGCGGGCGGTGGGGGTGCGAGGCCGGGGGGTGGGTGCGAGGCGTGGGGGAGGTGCGAGGCGGGCGGGGCGGGGGGCGCGAGGCGGGAGGGCGCACGCGCAGAAGGCTGGCTGGGGTGACGCGGCGCCGGGCTTGGGCTTCTGTATTCCGCGTGTCTGGAGGAAGGTCCGGAGGTGGGCGGGAGCCCTGCGGGGATTTCCTCTTCCCCCAGGACTAGCTGTCATCTTCGTTTTTCAGAAGGGAGGACCTGACTCCTTTCAGAAT... | AGAACGAGTGGCCGAGGGGACCCCTGCGGCCCTGCGCGCCTGTGAGTCTCCCGGGCGGGCGGGCGGTGGGGGTGCGAGGCCGGGGGGTGGGTGCGAGGCGTGGGGGAGGTGCGAGGCGGGCGGGGCGGGGGGCGCGAGGCGGGAGGGCGCACGCGCAGAAGGCTGGCTGGGGTGACGCGGCGCCGGGCTTGGGCTTCTGTATTCCGCGTGTCTGGAGGAAGGTCCGGAGGTGGGCGGGAGCCCTGCGGGGATTTCCTCTTCCCCCAGGACTAGCTGTCATCTTCGTTTTTCAGAAGGGAGGACCTGACTCCTTTCAGAAT... |
Task1_train_44926 | A mutation on Chromosome 17 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CTCAGTTTAAATTTTCTTCAAATTACTAGTGTGGTTTCTGTCCCCTGCCTGGACACTTGCAGATGTGACCCTCCTTGGACCAAAGCTTCCAAGGAGACTTTAGAGAGCCTCCTCAGAGTCAGCACAAGGGAAGAAGAGGAGCTAGAGTCTCTTTCTCATTCAGGGCTCGAGGGCAGAAAAGACAGACACAGAAACACATACTAACTGCTCTACCTGGCCCAAGAGAGGTTTGAACTTGGCACCTCCCCCTACAGCTGCCCCTCGGTCCAGCCTGAAGGTCATCAATCTGGCTCCCATAACAGACCAAATCCCCCTTCCCA... | CTCAGTTTAAATTTTCTTCAAATTACTAGTGTGGTTTCTGTCCCCTGCCTGGACACTTGCAGATGTGACCCTCCTTGGACCAAAGCTTCCAAGGAGACTTTAGAGAGCCTCCTCAGAGTCAGCACAAGGGAAGAAGAGGAGCTAGAGTCTCTTTCTCATTCAGGGCTCGAGGGCAGAAAAGACAGACACAGAAACACATACTAACTGCTCTACCTGGCCCAAGAGAGGTTTGAACTTGGCACCTCCCCCTACAGCTGCCCCTCGGTCCAGCCTGAAGGTCATCAATCTGGCTCCCATAACAGACCAAATCCCCCTTCCCA... |
Task1_train_44927 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | GCCCTTAGTGCACCCAGAGTATACCGGGAAGGTCTCAGGGCAGGCTTCCTTGACCCTGGCGGGGTGATGTGGTCACTCCCTGAGGGACTCCTGTCAGGGCCCGGTCGCCCATGCTGGGTGGCCCCCATCCCATCTCAGGGCTAACCTTTCTCAGCTCCAGCAGAAAGCACCACCTCAAGTCCAGGATGGGCAGCCCCACTGTGGCCTGACCACCCCCCATGCCAGGGGCCCCAGTAACCCCAGCCAGGCTGTCCCTGCACTCCTTCTTCTCCCAGGTCCTGCCCCTCCTGGGAGTCAGAGCCACAGGAAGGCCCTTGTCC... | GCCCTTAGTGCACCCAGAGTATACCGGGAAGGTCTCAGGGCAGGCTTCCTTGACCCTGGCGGGGTGATGTGGTCACTCCCTGAGGGACTCCTGTCAGGGCCCGGTCGCCCATGCTGGGTGGCCCCCATCCCATCTCAGGGCTAACCTTTCTCAGCTCCAGCAGAAAGCACCACCTCAAGTCCAGGATGGGCAGCCCCACTGTGGCCTGACCACCCCCCATGCCAGGGGCCCCAGTAACCCCAGCCAGGCTGTCCCTGCACTCCTTCTTCTCCCAGGTCCTGCCCCTCCTGGGAGTCAGAGCCACAGGAAGGCCCTTGTCC... |
Task1_train_44928 | Chromosome 17 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AGCCTCATGGGCAGACTGGGTCAGGACCCAACTTGAGAGGGCTCAGGGAAGCCTCAAGCCCTGGGCAAGCCCCTCTCTCCAGGAGCCACATACCCACTCAAATGAGTACCCCCCCATGAGAAGTTGCAAGACCTTTTCTGACTCAGCATTCTGGAGGGCTCAGGTGACCCTCATGGGGAAGGTCACTGACTCTGGAGACTGAAGCCCCAGTGTGCGCAGCTCGAGCCACCAGCCCCAGCCTGGAAGGGCCAGGTTCTCTCATACCTGCTGTCCCCACAGATCTCTCTCGGGCTCACCCTGCGCCTGTGGGACGTGTATTT... | AGCCTCATGGGCAGACTGGGTCAGGACCCAACTTGAGAGGGCTCAGGGAAGCCTCAAGCCCTGGGCAAGCCCCTCTCTCCAGGAGCCACATACCCACTCAAATGAGTACCCCCCCATGAGAAGTTGCAAGACCTTTTCTGACTCAGCATTCTGGAGGGCTCAGGTGACCCTCATGGGGAAGGTCACTGACTCTGGAGACTGAAGCCCCAGTGTGCGCAGCTCGAGCCACCAGCCCCAGCCTGGAAGGGCCAGGTTCTCTCATACCTGCTGTCCCCACAGATCTCTCTCGGGCTCACCCTGCGCCTGTGGGACGTGTATTT... |
Task1_train_44929 | Given this variant on Chromosome 17, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GTTGCAAGACCTTTTCTGACTCAGCATTCTGGAGGGCTCAGGTGACCCTCATGGGGAAGGTCACTGACTCTGGAGACTGAAGCCCCAGTGTGCGCAGCTCGAGCCACCAGCCCCAGCCTGGAAGGGCCAGGTTCTCTCATACCTGCTGTCCCCACAGATCTCTCTCGGGCTCACCCTGCGCCTGTGGGACGTGTATTTGGTGGAAGGAGAACAGGTGTTGATGCCAATAACCAGCATTGCTCTTAAGGTTCAGCAGAGTAAGTCTACGTGTGCCCAGTGGGGCCTGGGGAGCCCTGCAGTCAGACCCCGACTGGCCCAAG... | GTTGCAAGACCTTTTCTGACTCAGCATTCTGGAGGGCTCAGGTGACCCTCATGGGGAAGGTCACTGACTCTGGAGACTGAAGCCCCAGTGTGCGCAGCTCGAGCCACCAGCCCCAGCCTGGAAGGGCCAGGTTCTCTCATACCTGCTGTCCCCACAGATCTCTCTCGGGCTCACCCTGCGCCTGTGGGACGTGTATTTGGTGGAAGGAGAACAGGTGTTGATGCCAATAACCAGCATTGCTCTTAAGGTTCAGCAGAGTAAGTCTACGTGTGCCCAGTGGGGCCTGGGGAGCCCTGCAGTCAGACCCCGACTGGCCCAAG... |
Task1_train_44930 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | AGGTCACTGACTCTGGAGACTGAAGCCCCAGTGTGCGCAGCTCGAGCCACCAGCCCCAGCCTGGAAGGGCCAGGTTCTCTCATACCTGCTGTCCCCACAGATCTCTCTCGGGCTCACCCTGCGCCTGTGGGACGTGTATTTGGTGGAAGGAGAACAGGTGTTGATGCCAATAACCAGCATTGCTCTTAAGGTTCAGCAGAGTAAGTCTACGTGTGCCCAGTGGGGCCTGGGGAGCCCTGCAGTCAGACCCCGACTGGCCCAAGGGCAGCTTCCTCACACTGTCCTCATGATCCTCTGTTCTGGCCCAGAGGGAGGTCTGG... | AGGTCACTGACTCTGGAGACTGAAGCCCCAGTGTGCGCAGCTCGAGCCACCAGCCCCAGCCTGGAAGGGCCAGGTTCTCTCATACCTGCTGTCCCCACAGATCTCTCTCGGGCTCACCCTGCGCCTGTGGGACGTGTATTTGGTGGAAGGAGAACAGGTGTTGATGCCAATAACCAGCATTGCTCTTAAGGTTCAGCAGAGTAAGTCTACGTGTGCCCAGTGGGGCCTGGGGAGCCCTGCAGTCAGACCCCGACTGGCCCAAGGGCAGCTTCCTCACACTGTCCTCATGATCCTCTGTTCTGGCCCAGAGGGAGGTCTGG... |
Task1_train_44931 | This alteration on Chromosome 17 may affect genome function. Does it lead to a disease or is it benign? | Benign | CCCTGTGGGCACTCAGGGTGTGCCCAGCCTGGCCCTGGCTCAGGGAGGACCTCAGGGTTCCTGGAGATTCCTGGAGTGGAAGTCAATGCCCCGGCTCCCAACGGACCTGGATATAGGGGGCCCTTGGTTCCCCCATTATGATTTTGAATGGAGCTGCTGGGTCCGTGCCATATCCCAGGAGGACCAGCTGGCCACCTGCTGGCAGGCTGAACACTGCGGAGAGGGTGAGGTTGGCTTTCACTGCACTGAGCCACAATGTGGGCATGGACTTCCCGGCCCTGCAGTGCACCCAGCACTGATTCCGACCGGGATACCTCCTT... | CCCTGTGGGCACTCAGGGTGTGCCCAGCCTGGCCCTGGCTCAGGGAGGACCTCAGGGTTCCTGGAGATTCCTGGAGTGGAAGTCAATGCCCCGGCTCCCAACGGACCTGGATATAGGGGGCCCTTGGTTCCCCCATTATGATTTTGAATGGAGCTGCTGGGTCCGTGCCATATCCCAGGAGGACCAGCTGGCCACCTGCTGGCAGGCTGAACACTGCGGAGAGGGTGAGGTTGGCTTTCACTGCACTGAGCCACAATGTGGGCATGGACTTCCCGGCCCTGCAGTGCACCCAGCACTGATTCCGACCGGGATACCTCCTT... |
Task1_train_44932 | The following genetic variant occurs on Chromosome 17. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TAGTAGAGACAGGGTCTCTCTATGTTGGTTAGGTTGGTCTTGAACTCCCGACCTCAGGTGATCCACCCACCTTGGCCTCCCAAAGTGCTGGAATTACAGGCATGAGCCACCGCATCCAGCCAGAAATGTACCCTTTTACCTCTGATTTTTATTTTTCTCTGAATTAGTAGCCGTTGGCTTAAAGTTCCTTTCTTTTTCTTTTTTTTTTGAGACAGATTCTTGCTGTTGTTGCCCAGGCTGGAGTGCAATGGCACGATCTCGGCTCACTGTACTCTCTGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGT... | TAGTAGAGACAGGGTCTCTCTATGTTGGTTAGGTTGGTCTTGAACTCCCGACCTCAGGTGATCCACCCACCTTGGCCTCCCAAAGTGCTGGAATTACAGGCATGAGCCACCGCATCCAGCCAGAAATGTACCCTTTTACCTCTGATTTTTATTTTTCTCTGAATTAGTAGCCGTTGGCTTAAAGTTCCTTTCTTTTTCTTTTTTTTTTGAGACAGATTCTTGCTGTTGTTGCCCAGGCTGGAGTGCAATGGCACGATCTCGGCTCACTGTACTCTCTGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGT... |
Task1_train_44933 | Chromosome 17 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | ATGGACATTTTGAGGGAGATATTTATATGTTGTGGAGGGTTGTTTAAGCCACGTCTCGGGCCTCCACCCACTAGATGCTAATAGTCCTATAACTAGAATTGTGACAACCAGAAATGTCTCCAAGCATTGCCAAATGTTCCTTGGGGGACAAAACCTCCCTGAGTTCAGAAACGCTGCTGTGCAGGAAGGCCGTTACCCAGCCATATCTAGAGTAGCAAGAATTTGGAAGGAATATAAATGTTCTGTAATAGGACATTGGATGCTGAGATATTATGCACACAACCATTAAGGAAACTGGCAAGCTAGAATAAAAAATATGG... | ATGGACATTTTGAGGGAGATATTTATATGTTGTGGAGGGTTGTTTAAGCCACGTCTCGGGCCTCCACCCACTAGATGCTAATAGTCCTATAACTAGAATTGTGACAACCAGAAATGTCTCCAAGCATTGCCAAATGTTCCTTGGGGGACAAAACCTCCCTGAGTTCAGAAACGCTGCTGTGCAGGAAGGCCGTTACCCAGCCATATCTAGAGTAGCAAGAATTTGGAAGGAATATAAATGTTCTGTAATAGGACATTGGATGCTGAGATATTATGCACACAACCATTAAGGAAACTGGCAAGCTAGAATAAAAAATATGG... |
Task1_train_44934 | Here is a variant on Chromosome 17. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TCTGACTTCTGCTACCAGCGTCATATTCTTGCTGTTGACAAAATTCTCTTTGCACCAATCCTGAATAGGAGAAAGAGTGATATCACAATCCACTCATTCACCATTTATATGTTCACAGAGACGGGGTCTTGCTCTGTTCCCTAGGCTGGAGTGCAGTGATACAATCATAGCTCACTGCAAACCAATCCTCCCACCTCAGCCTCCCAGATAGCTTGAACTATCTGCACATGCCACCATGCCCAGCTAACAATCCTCTCATCTCTATAGAGAAAATATAACAACATTTTTAGAACACAGTTGAATTCAGAGAAAAAACTTCA... | TCTGACTTCTGCTACCAGCGTCATATTCTTGCTGTTGACAAAATTCTCTTTGCACCAATCCTGAATAGGAGAAAGAGTGATATCACAATCCACTCATTCACCATTTATATGTTCACAGAGACGGGGTCTTGCTCTGTTCCCTAGGCTGGAGTGCAGTGATACAATCATAGCTCACTGCAAACCAATCCTCCCACCTCAGCCTCCCAGATAGCTTGAACTATCTGCACATGCCACCATGCCCAGCTAACAATCCTCTCATCTCTATAGAGAAAATATAACAACATTTTTAGAACACAGTTGAATTCAGAGAAAAAACTTCA... |
Task1_train_44935 | A genomic change on Chromosome 17 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CCACGCTGCAGCCTGGGTAACAGAGTGCAAAAAAAAAAAAAAATCAAGACGGAATTTCAGTCTTGTTCAAGTGACTCTCCTGCCTCAGCCTCCCTAGTAGCTGGAACGACAGGCATGTGCCACCATGCCTGGATCATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCACGTTGGCCAGGCTGGTCTCGATCTCCTGACCTCAGGTGATCCACCGGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTGCCGGGCCAATTATCTGGATACTTTCAGATCATATTTCTGCCAACTCCCTGAAATACA... | CCACGCTGCAGCCTGGGTAACAGAGTGCAAAAAAAAAAAAAAATCAAGACGGAATTTCAGTCTTGTTCAAGTGACTCTCCTGCCTCAGCCTCCCTAGTAGCTGGAACGACAGGCATGTGCCACCATGCCTGGATCATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCACGTTGGCCAGGCTGGTCTCGATCTCCTGACCTCAGGTGATCCACCGGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTGCCGGGCCAATTATCTGGATACTTTCAGATCATATTTCTGCCAACTCCCTGAAATACA... |
Task1_train_44936 | Here’s a variant located on Chromosome 17. What is the predicted biological effect — harmless or disease-causing? | Benign | GTAAAGTGTGATTGTAAAGCACAGGCTGACATTGGGGAACCGTGGATGTCATACTTGTGGCACCGAAACAAGTGTCCGGGGGCAAGATATCAAGGCACAGAGTGATATGGGATTATGGGAAGTCAGAACTGAGAAATGGCAAGGCCCTGATATTGGAAAACAGGGCGTTTGTAAAGACCCAGGGGGAAAATTCCAGAGCTTAGCTGGGGGGCCGTACTCGGTCTTCAAAATGGAGGCAAGTGGAAACGAAATACTGAGGGGCAGTAGGTAATGCCACAATGGGATAGTGGCTGATCTGCCATAAGGGATGGTAGACTCGG... | GTAAAGTGTGATTGTAAAGCACAGGCTGACATTGGGGAACCGTGGATGTCATACTTGTGGCACCGAAACAAGTGTCCGGGGGCAAGATATCAAGGCACAGAGTGATATGGGATTATGGGAAGTCAGAACTGAGAAATGGCAAGGCCCTGATATTGGAAAACAGGGCGTTTGTAAAGACCCAGGGGGAAAATTCCAGAGCTTAGCTGGGGGGCCGTACTCGGTCTTCAAAATGGAGGCAAGTGGAAACGAAATACTGAGGGGCAGTAGGTAATGCCACAATGGGATAGTGGCTGATCTGCCATAAGGGATGGTAGACTCGG... |
Task1_train_44937 | A variant on Chromosome 17 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | ATTATCACTAGGTGCTATTTGATTTTAAAAATATTTGTTATATTCATCAGGTGTTCGGACGGTTCAAGTTTATGTCTTCCAGGCTACAACAGTTTCAGAGAAAAATAATTAGTCCAGTGTTCCAGCCTGTGCCACTGCAGAAAAGATGGAGTCCCTATAAGTCATTCGATCAGGTACGAAGACATTTCTATGCCTCCAGAGCAGGTAGGGATGATGGCCCCTGTTCAGCATGAAGCAGTGACAGAAGATAGATCTCTGTCCTTCTACAACCTCTTAAGATTAAGGACGAGTATGTAATGTCTGAGGTGGGGATAAGATAG... | ATTATCACTAGGTGCTATTTGATTTTAAAAATATTTGTTATATTCATCAGGTGTTCGGACGGTTCAAGTTTATGTCTTCCAGGCTACAACAGTTTCAGAGAAAAATAATTAGTCCAGTGTTCCAGCCTGTGCCACTGCAGAAAAGATGGAGTCCCTATAAGTCATTCGATCAGGTACGAAGACATTTCTATGCCTCCAGAGCAGGTAGGGATGATGGCCCCTGTTCAGCATGAAGCAGTGACAGAAGATAGATCTCTGTCCTTCTACAACCTCTTAAGATTAAGGACGAGTATGTAATGTCTGAGGTGGGGATAAGATAG... |
Task1_train_44938 | A variant on Chromosome 17 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | AAGTGCTGGGATTATAGGCGTGACCCACTGCGCCTGGCCCATAATGGCCTTTTGACTTGTCTCTCTGCTTTCACTCTTGCCTGCTTATCATTCGTTCTCACCCAGCAGCCAGAGGCATCTTTATGAAAGTAAATCAGGTCTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTTGCTCTATCACCTAGGCTGGAGTGCAGTGGTGCACTCTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCCCCTGAGTAGCTGGCATTACAGGCATACACCACCACACCCAGCTAATTTTT... | AAGTGCTGGGATTATAGGCGTGACCCACTGCGCCTGGCCCATAATGGCCTTTTGACTTGTCTCTCTGCTTTCACTCTTGCCTGCTTATCATTCGTTCTCACCCAGCAGCCAGAGGCATCTTTATGAAAGTAAATCAGGTCTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTTGCTCTATCACCTAGGCTGGAGTGCAGTGGTGCACTCTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCCCCTGAGTAGCTGGCATTACAGGCATACACCACCACACCCAGCTAATTTTT... |
Task1_train_44939 | This variant is found on Chromosome 17. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GAGCAGTTCCCTGCTTTTTATTTTTCTCATTTGATTTTTCTCTTTCTACTAGCTTCTAAATAATTTTTCTTATATATATGCCTTGATTACCTTAATATATGCATACTGTAAAGTTAATACCTTTATTTTGAGGTGATACTAAAAATACATTGAACTACTGGGATGATACTACAACATATCAACTAACAAATGAGAAATTAAAAATAAATTCTCATTTACCTCTATTCCTGGGAAATAAAGAAATTAAGACAAGAAAAAATATTAAAAACCCATTTAATATCTAGCTAAACTGTACAAATCATAAAAGTGCTTATAACTGA... | GAGCAGTTCCCTGCTTTTTATTTTTCTCATTTGATTTTTCTCTTTCTACTAGCTTCTAAATAATTTTTCTTATATATATGCCTTGATTACCTTAATATATGCATACTGTAAAGTTAATACCTTTATTTTGAGGTGATACTAAAAATACATTGAACTACTGGGATGATACTACAACATATCAACTAACAAATGAGAAATTAAAAATAAATTCTCATTTACCTCTATTCCTGGGAAATAAAGAAATTAAGACAAGAAAAAATATTAAAAACCCATTTAATATCTAGCTAAACTGTACAAATCATAAAAGTGCTTATAACTGA... |
Task1_train_44940 | A variant affecting Chromosome 17 has been observed. Determine if it's benign or associated with disease. | Benign | AAATGAGTGGACCTTGTTTGGATCCTGATAAGAACACACCAACTGGCCAGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGAAGGTGGATCGTCTGAGGTCAGGAGTTCGAGACCAGCCTGTCCAATATGGTGAAACCCCCATCTCTACTAAAAATACAATTTTCATTTTTCACACGTGGTGGCATGTGACTGTAGTCCCAGCTACTAGAGAGGCTGAGGCTGGAGAATCGCTTGAACCTGGGAGGTGGAGGTTGAGGTAAGCCAAGATTGTGCCATTGCACTCCAGCCTGAGTGACAGAGCAAG... | AAATGAGTGGACCTTGTTTGGATCCTGATAAGAACACACCAACTGGCCAGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGAAGGTGGATCGTCTGAGGTCAGGAGTTCGAGACCAGCCTGTCCAATATGGTGAAACCCCCATCTCTACTAAAAATACAATTTTCATTTTTCACACGTGGTGGCATGTGACTGTAGTCCCAGCTACTAGAGAGGCTGAGGCTGGAGAATCGCTTGAACCTGGGAGGTGGAGGTTGAGGTAAGCCAAGATTGTGCCATTGCACTCCAGCCTGAGTGACAGAGCAAG... |
Task1_train_44941 | A mutation found on Chromosome 17 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AATTATCGCTGCATGTTGGCATGCTCCTGTAGTCTCAGCTCCTAGCGGGGCTGAGGTAAGAGGATCCCTTAAACTCGGGTGGTCCAGGCTGCAGTGAGCTGTGATTGCACCACTGCACTCCAGCCTAGGGGACAGAGCGAGACTCCGTCTCAGACAACAACAAACCAAAAAAAAAAAAAAATACCCCACACCCACTCACAAGAAGATAGCCTTGATATATAAAGAAAATAAAACTGACTATAAAATAAAATGTACAATATGGTTCGATTTCGCCATAGACATGTGCACAGAAAAAAGACTGGGGTTCTTACAATTGACCA... | AATTATCGCTGCATGTTGGCATGCTCCTGTAGTCTCAGCTCCTAGCGGGGCTGAGGTAAGAGGATCCCTTAAACTCGGGTGGTCCAGGCTGCAGTGAGCTGTGATTGCACCACTGCACTCCAGCCTAGGGGACAGAGCGAGACTCCGTCTCAGACAACAACAAACCAAAAAAAAAAAAAAATACCCCACACCCACTCACAAGAAGATAGCCTTGATATATAAAGAAAATAAAACTGACTATAAAATAAAATGTACAATATGGTTCGATTTCGCCATAGACATGTGCACAGAAAAAAGACTGGGGTTCTTACAATTGACCA... |
Task1_train_44942 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | TGAGGTGGGTGGATCACCTCGGATCAGGAGTTCGAGACCAGCCTGACTAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAAATTAGCAGGGCTTCGTGGCGGGCACCTGTAGTCCCAGCGACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCAGAGCTTGCAGTGAGTGGAGATCACGCCACTGCACTCCAGCCTGGGTGACCGAGCAAGACTCTGTCTCAAAACAAAACACAACAAAAAACAAAAAACAACAAACAAAAAACAAAAACAAAAACAAACAAAAAACCCAACCTAACAGGTACCA... | TGAGGTGGGTGGATCACCTCGGATCAGGAGTTCGAGACCAGCCTGACTAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAAATTAGCAGGGCTTCGTGGCGGGCACCTGTAGTCCCAGCGACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCAGAGCTTGCAGTGAGTGGAGATCACGCCACTGCACTCCAGCCTGGGTGACCGAGCAAGACTCTGTCTCAAAACAAAACACAACAAAAAACAAAAAACAACAAACAAAAAACAAAAACAAAAACAAACAAAAAACCCAACCTAACAGGTACCA... |
Task1_train_44943 | Given this variant on Chromosome 17, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TTGTTGTTGTTTTTGTTTTGTTTTGTTTTTTGAGATGAAGTTTTACTCTTGTTGACCAGGCTGGAGTGCAATGACGTGATCTTGGCTCACTGCAACCTCCGCCTCCCAGGTTCAATCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTATAGGCGCCCGCCACCACGCCCAGCTAGTTTTTTTGTATTTTTAGTAGAGATGAGGTTTCACCATGTTGGCCAGGCTGGTCTGGAACTCCTGACCTCAGGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACCGTGCCCGACCACAG... | TTGTTGTTGTTTTTGTTTTGTTTTGTTTTTTGAGATGAAGTTTTACTCTTGTTGACCAGGCTGGAGTGCAATGACGTGATCTTGGCTCACTGCAACCTCCGCCTCCCAGGTTCAATCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTATAGGCGCCCGCCACCACGCCCAGCTAGTTTTTTTGTATTTTTAGTAGAGATGAGGTTTCACCATGTTGGCCAGGCTGGTCTGGAACTCCTGACCTCAGGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACCGTGCCCGACCACAG... |
Task1_train_44944 | This alteration on Chromosome 17 may affect genome function. Does it lead to a disease or is it benign? | Benign | CTGGCACATATAGGTGCTCAACAAATAGTTGAATGAGTGAATGAAAGCATGTCTTGGAGGAAACAGATGCTCACAATACCAGGTGATAAGAGCTGTACGTGATAGGAAATTGCAAAGCAAGTGACCAATAGTGAGGCTCACCAAATGCAAGCTTAGTCGGTGAAGGCTTCCCAGAGGAGGTGATTCCAGAGTTCACCCAGGGAAGCAAAGGTCAAGGGGTATTTAGGGTAGGGGAAATAGTGCAAGTCCAGGCCTAGAGCTGAGGGAAAGCAAGGTGTACTGCCCACTCAGCTGTGTATCCCTGAGGAGAGCCAGAATTG... | CTGGCACATATAGGTGCTCAACAAATAGTTGAATGAGTGAATGAAAGCATGTCTTGGAGGAAACAGATGCTCACAATACCAGGTGATAAGAGCTGTACGTGATAGGAAATTGCAAAGCAAGTGACCAATAGTGAGGCTCACCAAATGCAAGCTTAGTCGGTGAAGGCTTCCCAGAGGAGGTGATTCCAGAGTTCACCCAGGGAAGCAAAGGTCAAGGGGTATTTAGGGTAGGGGAAATAGTGCAAGTCCAGGCCTAGAGCTGAGGGAAAGCAAGGTGTACTGCCCACTCAGCTGTGTATCCCTGAGGAGAGCCAGAATTG... |
Task1_train_44945 | A change on Chromosome 17 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | ATGTAAAGGATCATGTAGCCCAAGTCCTGCCAGTGCCTGGTGAGATGGCATTAGAAGGGTCCAGCCCTGCCCAGTGCAGGCCACCTGATGCCCAGAAGCCTGCCCTGCCCGCAGCTGCCCTCCTGAGACGTCAGAGGGACGAGTCTGAGGCGTGCTAGGGAGAACAAGGGGGACCCCGAATCCCCTCTCTGGGCTGAGCCCTGGACATCTCCCCTGGATCAGGCCTGCAGATGCCACAGGCCCATATCCAAACTCATCTCCTCACCCCTGCCCCTCTGCTCACAGCCACTTCAGAGTCAGAGACAGGCGCCTTTCATTCT... | ATGTAAAGGATCATGTAGCCCAAGTCCTGCCAGTGCCTGGTGAGATGGCATTAGAAGGGTCCAGCCCTGCCCAGTGCAGGCCACCTGATGCCCAGAAGCCTGCCCTGCCCGCAGCTGCCCTCCTGAGACGTCAGAGGGACGAGTCTGAGGCGTGCTAGGGAGAACAAGGGGGACCCCGAATCCCCTCTCTGGGCTGAGCCCTGGACATCTCCCCTGGATCAGGCCTGCAGATGCCACAGGCCCATATCCAAACTCATCTCCTCACCCCTGCCCCTCTGCTCACAGCCACTTCAGAGTCAGAGACAGGCGCCTTTCATTCT... |
Task1_train_44946 | 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 | AAGGGTCCAGCCCTGCCCAGTGCAGGCCACCTGATGCCCAGAAGCCTGCCCTGCCCGCAGCTGCCCTCCTGAGACGTCAGAGGGACGAGTCTGAGGCGTGCTAGGGAGAACAAGGGGGACCCCGAATCCCCTCTCTGGGCTGAGCCCTGGACATCTCCCCTGGATCAGGCCTGCAGATGCCACAGGCCCATATCCAAACTCATCTCCTCACCCCTGCCCCTCTGCTCACAGCCACTTCAGAGTCAGAGACAGGCGCCTTTCATTCTTCCCTGTTCCCTGTGCCTCCCTCCCTCCTCCTCCTCCAGGAAGAAAGCCTTTCG... | AAGGGTCCAGCCCTGCCCAGTGCAGGCCACCTGATGCCCAGAAGCCTGCCCTGCCCGCAGCTGCCCTCCTGAGACGTCAGAGGGACGAGTCTGAGGCGTGCTAGGGAGAACAAGGGGGACCCCGAATCCCCTCTCTGGGCTGAGCCCTGGACATCTCCCCTGGATCAGGCCTGCAGATGCCACAGGCCCATATCCAAACTCATCTCCTCACCCCTGCCCCTCTGCTCACAGCCACTTCAGAGTCAGAGACAGGCGCCTTTCATTCTTCCCTGTTCCCTGTGCCTCCCTCCCTCCTCCTCCTCCAGGAAGAAAGCCTTTCG... |
Task1_train_44947 | Chromosome 17 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CACCAGCCCTAGAGCCTAGAGCCCAGAGCCCTCGACATGCAAATCAGCCAGCCCTGCATGGTTCTCCTGCTCTGCCCTGCCTTTCCAGAGAAAAAACCAACAAGGGCTCTGGGCCTTGCAGCTTTGGGGGGCTCAGTCCACTCTGCCCACCACCTCCCTGGGCTCAGGTCTGCAGCCACTCTGCAAGCTCTTCCATACCTCAGTTGCTATTTTCTGAGGTGGAGGCGCCTGTGACACCAGCCTTCCTATGGCCTGGAATCCAGCCTTGAGTTGGATTCCTGGCCCTTCTGTCTCCTGACCAAACCAAGTGCTTCCCCCGT... | CACCAGCCCTAGAGCCTAGAGCCCAGAGCCCTCGACATGCAAATCAGCCAGCCCTGCATGGTTCTCCTGCTCTGCCCTGCCTTTCCAGAGAAAAAACCAACAAGGGCTCTGGGCCTTGCAGCTTTGGGGGGCTCAGTCCACTCTGCCCACCACCTCCCTGGGCTCAGGTCTGCAGCCACTCTGCAAGCTCTTCCATACCTCAGTTGCTATTTTCTGAGGTGGAGGCGCCTGTGACACCAGCCTTCCTATGGCCTGGAATCCAGCCTTGAGTTGGATTCCTGGCCCTTCTGTCTCCTGACCAAACCAAGTGCTTCCCCCGT... |
Task1_train_44948 | A variant affecting Chromosome 17 has been observed. Determine if it's benign or associated with disease. | Benign | CATAAATCTACAAAAAGAGACACACGTGAGTGAGAAATGCCCAAGATTTTCAGAAGATAAACGCACACAGAAGAATCATAACTGATTTAGCAGCATAGAGGGAGCTGAAACCTAAGAGTCTGTAAGTGGGGGTGGGAGGGATGCCAGGCAAAAACAAGCTGATTTGTCCTATAAAACATCGTGAAGGCTCAGGAAGTTAAGAGTGCTGAGAATCATGAAGGCAGAGTGCAGTATGGGGTAGAAAATGAGGAGACTGGCTGAAAATTTGCAGAACAAGCTGTTGGACTGACACACTCCACCCCTATTCGCAGCTAAGTGAC... | CATAAATCTACAAAAAGAGACACACGTGAGTGAGAAATGCCCAAGATTTTCAGAAGATAAACGCACACAGAAGAATCATAACTGATTTAGCAGCATAGAGGGAGCTGAAACCTAAGAGTCTGTAAGTGGGGGTGGGAGGGATGCCAGGCAAAAACAAGCTGATTTGTCCTATAAAACATCGTGAAGGCTCAGGAAGTTAAGAGTGCTGAGAATCATGAAGGCAGAGTGCAGTATGGGGTAGAAAATGAGGAGACTGGCTGAAAATTTGCAGAACAAGCTGTTGGACTGACACACTCCACCCCTATTCGCAGCTAAGTGAC... |
Task1_train_44949 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | ACCGTGTTCTATCTTAAATTATAGTTAATTACATAACTTCTCTATTGACTATAAATAAGCAAGGGCTGGGATTATGGCCTATTTGCCCTTTTTAAAGTCTCCATAGAGCTCATAACACTGTCACATACAAAACTAGCAAGTGATATATAATTGACACATATATAATTTATGAATGAATAAGAAAAAATAGAAGAGCTCACTATAAGCTATATAGTTTGACTGAAACGTTTAATAAACTACATTTTATGTATTTATTCTATTTTTAAAAATAATCTACATTTTAAATAACCAACTTTAAATGTAGGAAAGAGAAGAAAGGG... | ACCGTGTTCTATCTTAAATTATAGTTAATTACATAACTTCTCTATTGACTATAAATAAGCAAGGGCTGGGATTATGGCCTATTTGCCCTTTTTAAAGTCTCCATAGAGCTCATAACACTGTCACATACAAAACTAGCAAGTGATATATAATTGACACATATATAATTTATGAATGAATAAGAAAAAATAGAAGAGCTCACTATAAGCTATATAGTTTGACTGAAACGTTTAATAAACTACATTTTATGTATTTATTCTATTTTTAAAAATAATCTACATTTTAAATAACCAACTTTAAATGTAGGAAAGAGAAGAAAGGG... |
Task1_train_44950 | This alteration occurs on Chromosome 17. Is it associated with a disease or is it a benign variant? | Benign | TGGGGTTTGGGGGTATCCATGGTGCCTTGCGGTCTTTCACAGGCTGCCGGTTCATTTTTAATCTGGATGAAACTGTTGTCTGCTGCACTCTGCTTTTACTGTGAGGTTGGCTTTGTCTACCTCTTTCAGCTTTGCGGAGTCCCTGTGAGAGATAAGTAAGAATTATAAGGCCACACAAATACCAAAGAAACTATGGTTTAACCTCTGACTCACTGAAGCTCCAAGTTCTCCATGTTATTCATGCATCCATTCGGTAAAACCTGAGTAGAAAGCACTGTGGCAGAAATTTGGGGGAGGGTGTAAATTTCATTGAAACAACC... | TGGGGTTTGGGGGTATCCATGGTGCCTTGCGGTCTTTCACAGGCTGCCGGTTCATTTTTAATCTGGATGAAACTGTTGTCTGCTGCACTCTGCTTTTACTGTGAGGTTGGCTTTGTCTACCTCTTTCAGCTTTGCGGAGTCCCTGTGAGAGATAAGTAAGAATTATAAGGCCACACAAATACCAAAGAAACTATGGTTTAACCTCTGACTCACTGAAGCTCCAAGTTCTCCATGTTATTCATGCATCCATTCGGTAAAACCTGAGTAGAAAGCACTGTGGCAGAAATTTGGGGGAGGGTGTAAATTTCATTGAAACAACC... |
Task1_train_44951 | This sequence variant lies on Chromosome 17. Is it clinically significant, and what condition might it cause if any? | Benign | TGAAACTGTTGTCTGCTGCACTCTGCTTTTACTGTGAGGTTGGCTTTGTCTACCTCTTTCAGCTTTGCGGAGTCCCTGTGAGAGATAAGTAAGAATTATAAGGCCACACAAATACCAAAGAAACTATGGTTTAACCTCTGACTCACTGAAGCTCCAAGTTCTCCATGTTATTCATGCATCCATTCGGTAAAACCTGAGTAGAAAGCACTGTGGCAGAAATTTGGGGGAGGGTGTAAATTTCATTGAAACAACCATGGTAGGGGCGGGGGGTGGAGGGTGTAGAATTTAAATCCCTGGCTCTGCCTGACACCTTTAAACAT... | TGAAACTGTTGTCTGCTGCACTCTGCTTTTACTGTGAGGTTGGCTTTGTCTACCTCTTTCAGCTTTGCGGAGTCCCTGTGAGAGATAAGTAAGAATTATAAGGCCACACAAATACCAAAGAAACTATGGTTTAACCTCTGACTCACTGAAGCTCCAAGTTCTCCATGTTATTCATGCATCCATTCGGTAAAACCTGAGTAGAAAGCACTGTGGCAGAAATTTGGGGGAGGGTGTAAATTTCATTGAAACAACCATGGTAGGGGCGGGGGGTGGAGGGTGTAGAATTTAAATCCCTGGCTCTGCCTGACACCTTTAAACAT... |
Task1_train_44952 | Given this variant on Chromosome 17, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TAAAAACTCCAATAATAGGCCAGGCGCTGTGGCTCATGCCTGTAATCCCAGCACTTCGGAAGGCTAAGACAGGTGGATCACTTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACGTGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGCACGCACCTGTAATCCCAGCTACTCAAGAGGCTGAGGCAGGAGAATTGCTTAAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATCACATCACTGCACTCCAGCCTGGACAACGGAGCGAGATTCCACTTCAAGAAAAAAAAAAAATCAGAA... | TAAAAACTCCAATAATAGGCCAGGCGCTGTGGCTCATGCCTGTAATCCCAGCACTTCGGAAGGCTAAGACAGGTGGATCACTTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACGTGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGCACGCACCTGTAATCCCAGCTACTCAAGAGGCTGAGGCAGGAGAATTGCTTAAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATCACATCACTGCACTCCAGCCTGGACAACGGAGCGAGATTCCACTTCAAGAAAAAAAAAAAATCAGAA... |
Task1_train_44953 | A variant was discovered on Chromosome 17. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | AAATCTCAGGCAAAAATAGAACTACCTGGGTCTGAAGTACTTTGGGGTCGCTCCTCCCATCAAGTTGGGTCCTAGGTGCTAGATGAACACAGGTTGAAGCTGGCTGGCCTGGTCCCATAATGTCAGGTAGTACAGAACAATAGTGACAGCCTTGTCATCCGGCAACAGTCTTCCCTAAAACCATTCCTAAAACGAAACAAAGCTACTTCAGACCAACAGCGTTGAACAAGGGAAAAGAACAGATAAAACACAGTGCCATGTGCATGTAGCAATATACTAGAAGTAGCCAATAGTAACCTCATACTGAGAGTGACTGCTTA... | AAATCTCAGGCAAAAATAGAACTACCTGGGTCTGAAGTACTTTGGGGTCGCTCCTCCCATCAAGTTGGGTCCTAGGTGCTAGATGAACACAGGTTGAAGCTGGCTGGCCTGGTCCCATAATGTCAGGTAGTACAGAACAATAGTGACAGCCTTGTCATCCGGCAACAGTCTTCCCTAAAACCATTCCTAAAACGAAACAAAGCTACTTCAGACCAACAGCGTTGAACAAGGGAAAAGAACAGATAAAACACAGTGCCATGTGCATGTAGCAATATACTAGAAGTAGCCAATAGTAACCTCATACTGAGAGTGACTGCTTA... |
Task1_train_44954 | A mutation on Chromosome 17 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | AGTTGGGTCCTAGGTGCTAGATGAACACAGGTTGAAGCTGGCTGGCCTGGTCCCATAATGTCAGGTAGTACAGAACAATAGTGACAGCCTTGTCATCCGGCAACAGTCTTCCCTAAAACCATTCCTAAAACGAAACAAAGCTACTTCAGACCAACAGCGTTGAACAAGGGAAAAGAACAGATAAAACACAGTGCCATGTGCATGTAGCAATATACTAGAAGTAGCCAATAGTAACCTCATACTGAGAGTGACTGCTTAATGACAGGTAAATGATAGTTTCTTCCATTTATAAAAGCAACCACACTTTGGAAGTTCCCAAT... | AGTTGGGTCCTAGGTGCTAGATGAACACAGGTTGAAGCTGGCTGGCCTGGTCCCATAATGTCAGGTAGTACAGAACAATAGTGACAGCCTTGTCATCCGGCAACAGTCTTCCCTAAAACCATTCCTAAAACGAAACAAAGCTACTTCAGACCAACAGCGTTGAACAAGGGAAAAGAACAGATAAAACACAGTGCCATGTGCATGTAGCAATATACTAGAAGTAGCCAATAGTAACCTCATACTGAGAGTGACTGCTTAATGACAGGTAAATGATAGTTTCTTCCATTTATAAAAGCAACCACACTTTGGAAGTTCCCAAT... |
Task1_train_44955 | A mutation located on Chromosome 17 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | AGATGAACACAGGTTGAAGCTGGCTGGCCTGGTCCCATAATGTCAGGTAGTACAGAACAATAGTGACAGCCTTGTCATCCGGCAACAGTCTTCCCTAAAACCATTCCTAAAACGAAACAAAGCTACTTCAGACCAACAGCGTTGAACAAGGGAAAAGAACAGATAAAACACAGTGCCATGTGCATGTAGCAATATACTAGAAGTAGCCAATAGTAACCTCATACTGAGAGTGACTGCTTAATGACAGGTAAATGATAGTTTCTTCCATTTATAAAAGCAACCACACTTTGGAAGTTCCCAATTTCAAAAACAAAAAAAAA... | AGATGAACACAGGTTGAAGCTGGCTGGCCTGGTCCCATAATGTCAGGTAGTACAGAACAATAGTGACAGCCTTGTCATCCGGCAACAGTCTTCCCTAAAACCATTCCTAAAACGAAACAAAGCTACTTCAGACCAACAGCGTTGAACAAGGGAAAAGAACAGATAAAACACAGTGCCATGTGCATGTAGCAATATACTAGAAGTAGCCAATAGTAACCTCATACTGAGAGTGACTGCTTAATGACAGGTAAATGATAGTTTCTTCCATTTATAAAAGCAACCACACTTTGGAAGTTCCCAATTTCAAAAACAAAAAAAAA... |
Task1_train_44956 | This variant is found on Chromosome 17. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | ACTAGAAGTAGCCAATAGTAACCTCATACTGAGAGTGACTGCTTAATGACAGGTAAATGATAGTTTCTTCCATTTATAAAAGCAACCACACTTTGGAAGTTCCCAATTTCAAAAACAAAAAAAAATAGGGGAACACTTACTATTTTAATAATAATCTCTTGAGCCCTTTCCATTCCAAATTTCAAATCTCAAAGGTCTCCAGCAAGGCGTTATTCCCAAAACAGAGCTTTGCCATGGTAAACTAGCATGTTCCAGCAGGGTGGTTTTTGGACAAGCAGTCTACATTAACAAGTCTTAATACTAGTCAGAAAGCAGTATGC... | ACTAGAAGTAGCCAATAGTAACCTCATACTGAGAGTGACTGCTTAATGACAGGTAAATGATAGTTTCTTCCATTTATAAAAGCAACCACACTTTGGAAGTTCCCAATTTCAAAAACAAAAAAAAATAGGGGAACACTTACTATTTTAATAATAATCTCTTGAGCCCTTTCCATTCCAAATTTCAAATCTCAAAGGTCTCCAGCAAGGCGTTATTCCCAAAACAGAGCTTTGCCATGGTAAACTAGCATGTTCCAGCAGGGTGGTTTTTGGACAAGCAGTCTACATTAACAAGTCTTAATACTAGTCAGAAAGCAGTATGC... |
Task1_train_44957 | This mutation is located on Chromosome 17. Is it associated with a disease or is it a benign polymorphism? | Benign | AAATGGGGCCCGGAGATCTGCCACTTTTAAATGGTCAGTACTTCCCTCCTGGCTGCTTCTAGGTGCCAAGGGCCAAATAGTCCATTCTCCACTAGAAAAAAACTAGGTGATCCCCACAGTTCCAGCATGCCTCAAGTGATGCTACACACACACATACACACACACGCACAAAGTCCAGGGACACCCACCCCTAAACTGTCCCCCTGTACAAAGTTCTGGGACTCTCCTTGCAATCTGGCCCTTTCCCACTGCTCCAGGAAACGTCCCAATTTGTCCCTCTACATACCCTGGGGCATCTCCACGAAAACCCTCTCTCCCCC... | AAATGGGGCCCGGAGATCTGCCACTTTTAAATGGTCAGTACTTCCCTCCTGGCTGCTTCTAGGTGCCAAGGGCCAAATAGTCCATTCTCCACTAGAAAAAAACTAGGTGATCCCCACAGTTCCAGCATGCCTCAAGTGATGCTACACACACACATACACACACACGCACAAAGTCCAGGGACACCCACCCCTAAACTGTCCCCCTGTACAAAGTTCTGGGACTCTCCTTGCAATCTGGCCCTTTCCCACTGCTCCAGGAAACGTCCCAATTTGTCCCTCTACATACCCTGGGGCATCTCCACGAAAACCCTCTCTCCCCC... |
Task1_train_44958 | Mutation context: Chromosome 17. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GCAGCCCCACAGCCATGGACACTCCTGTAGTCTGTCTGCCTCCCAACAAACCTGAGACACCCCCAGAGCCAGTCTTCTCCGCCATGGGCCCAGGCATCCTGGTCGAGGTGGGCACCTCCATCCTTGTGGGACCCTTGGCATCTGCAGGTCCGCCCACTGTCTCTCTTTCACCCCACAATTCTGAGCCAGTTTCCTCTTGCACAGGCCTAGGCACCCTGGGAGCCACGGGCACCCCACTAGCTGCAGACAGCCCCACAGTGCCAGGCATTCCTGCAGTTTGCTGCCTCCCTGACAAGCCTGAAAAGCCTCCATCACCAGGC... | GCAGCCCCACAGCCATGGACACTCCTGTAGTCTGTCTGCCTCCCAACAAACCTGAGACACCCCCAGAGCCAGTCTTCTCCGCCATGGGCCCAGGCATCCTGGTCGAGGTGGGCACCTCCATCCTTGTGGGACCCTTGGCATCTGCAGGTCCGCCCACTGTCTCTCTTTCACCCCACAATTCTGAGCCAGTTTCCTCTTGCACAGGCCTAGGCACCCTGGGAGCCACGGGCACCCCACTAGCTGCAGACAGCCCCACAGTGCCAGGCATTCCTGCAGTTTGCTGCCTCCCTGACAAGCCTGAAAAGCCTCCATCACCAGGC... |
Task1_train_44959 | This mutation is located on Chromosome 17. Is it associated with a disease or is it a benign polymorphism? | Benign | TGGTAGGTGGTTGTCTTAGCTCTCAACCAGGGGATCCGATTCCCATTTAAACTATCTAGGACGAAGCGAGTGAAAACCAGAGCCCTGTGTGGGGGATGCTTGAGGCAGAGCGGGTACAGCAGCCTGCATCCTGATCCCTCGGCTACCTGGCCTCCCTCACAGAGATAATGGCAAGGCTTGGGAAAGATGGGTCCAGCAGCCCACTGAGGGGTTCCCTTCATTTCTGAGCCTACCCTCCAGCTGCCCATGACCATCTCTGCATCTGGGCTTGGAGGAAGAGGTGGCCCATTGGCTGGGTTTTGGTGGTGTGTGGACATCGT... | TGGTAGGTGGTTGTCTTAGCTCTCAACCAGGGGATCCGATTCCCATTTAAACTATCTAGGACGAAGCGAGTGAAAACCAGAGCCCTGTGTGGGGGATGCTTGAGGCAGAGCGGGTACAGCAGCCTGCATCCTGATCCCTCGGCTACCTGGCCTCCCTCACAGAGATAATGGCAAGGCTTGGGAAAGATGGGTCCAGCAGCCCACTGAGGGGTTCCCTTCATTTCTGAGCCTACCCTCCAGCTGCCCATGACCATCTCTGCATCTGGGCTTGGAGGAAGAGGTGGCCCATTGGCTGGGTTTTGGTGGTGTGTGGACATCGT... |
Task1_train_44960 | 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 | ATCTGTGAAAGAAAGTGTCCCACGGAGATTCTCCAGGACTACTCTCACCCTCCTTGGAAAGGGAGCCGTGGGGCGGGGCAGGGGGGACAGAGCAGGGGGCTGGGACCACACCTCTAACGGGAGGGGGGGCGCGGAATCTGACCGATCAAAAAGCCCCATTCTCAAAGCTCCCTACCTGTGACAGGGACCTGAGTGGACCCTCCCCAGAGAGCTTTGCTCCAGCCAGACCCTTCAAGTACTCTGGTTTCTCAACCAGCCCAGGAAGAGCAGGGGGAGAAGGGGCCAGGTCAGGCAGAGGAGAGAGAGCAGAGGAAGGGAAG... | ATCTGTGAAAGAAAGTGTCCCACGGAGATTCTCCAGGACTACTCTCACCCTCCTTGGAAAGGGAGCCGTGGGGCGGGGCAGGGGGGACAGAGCAGGGGGCTGGGACCACACCTCTAACGGGAGGGGGGGCGCGGAATCTGACCGATCAAAAAGCCCCATTCTCAAAGCTCCCTACCTGTGACAGGGACCTGAGTGGACCCTCCCCAGAGAGCTTTGCTCCAGCCAGACCCTTCAAGTACTCTGGTTTCTCAACCAGCCCAGGAAGAGCAGGGGGAGAAGGGGCCAGGTCAGGCAGAGGAGAGAGAGCAGAGGAAGGGAAG... |
Task1_train_44961 | Here is a variant on Chromosome 17. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GAGAGATGGGGTCTGAGAGTCAAGGCGAGTGTTCAGTCCTCTCTGCAGGTGAGATGGGGTCTGAGAGTCAAGGCAAGTGTTCAGTCCTCTCTGCAGGTGAGATGGGGTCTGGGAGTCAAGGCGAGTGTTCAGTCCTCTCTGCAGGACAGATGGGGTCTGAGAGTCAAGGCGAGTGTTCAGTCCTCTCTGCAGGTGAGATGGGGTCTGGGAGTCAAGGCGAGTGTTCAGTCCTCCCTGCAGGTGAGATGGGGTCTGGGAGGGGCAAGTGTTCCATCTTCCCTGCAGGAGAGATGGGGTCTGGGAGTCACAGAGTGGGTCCA... | GAGAGATGGGGTCTGAGAGTCAAGGCGAGTGTTCAGTCCTCTCTGCAGGTGAGATGGGGTCTGAGAGTCAAGGCAAGTGTTCAGTCCTCTCTGCAGGTGAGATGGGGTCTGGGAGTCAAGGCGAGTGTTCAGTCCTCTCTGCAGGACAGATGGGGTCTGAGAGTCAAGGCGAGTGTTCAGTCCTCTCTGCAGGTGAGATGGGGTCTGGGAGTCAAGGCGAGTGTTCAGTCCTCCCTGCAGGTGAGATGGGGTCTGGGAGGGGCAAGTGTTCCATCTTCCCTGCAGGAGAGATGGGGTCTGGGAGTCACAGAGTGGGTCCA... |
Task1_train_44962 | A mutation found on Chromosome 17 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AGGACAGATGGGGTCTGAGAGTCAAGGCGAGTGTTCAGTCCTCTCTGCAGGTGAGATGGGGTCTGGGAGTCAAGGCGAGTGTTCAGTCCTCCCTGCAGGTGAGATGGGGTCTGGGAGGGGCAAGTGTTCCATCTTCCCTGCAGGAGAGATGGGGTCTGGGAGTCACAGAGTGGGTCCAGTCCTCCCTGCAGGAGAGATGGGGTCTGAGAGTTGGGGGACGAGGGTCTAGTCCTCCCTGCAGGTGAGATGGGGTCTGGGAGTCAAGGAGAGTGTTCAGTCCTCCCTGCAGGTGAGATGGGGTCTGGGAGGGGCAAGTGTTC... | AGGACAGATGGGGTCTGAGAGTCAAGGCGAGTGTTCAGTCCTCTCTGCAGGTGAGATGGGGTCTGGGAGTCAAGGCGAGTGTTCAGTCCTCCCTGCAGGTGAGATGGGGTCTGGGAGGGGCAAGTGTTCCATCTTCCCTGCAGGAGAGATGGGGTCTGGGAGTCACAGAGTGGGTCCAGTCCTCCCTGCAGGAGAGATGGGGTCTGAGAGTTGGGGGACGAGGGTCTAGTCCTCCCTGCAGGTGAGATGGGGTCTGGGAGTCAAGGAGAGTGTTCAGTCCTCCCTGCAGGTGAGATGGGGTCTGGGAGGGGCAAGTGTTC... |
Task1_train_44963 | A sequence alteration has been identified on Chromosome 17. Is it disease-inducing or harmless? | Benign | GTCATGGGCGGGACGGGCTGCTGTTCAGTCCTTTACGGAAGTCTGTTCGGATGTGGCGGTGGGAAGGCCAGCTGGAGACAGGGGCCAAATCAGTGAGTGGGTGGTGAGAGAAAGTGATGGCGTAGTGAGGACAAAGCCTGGAGAAGGTCCCTAGGGAGGCCCACAACTGTGCTTACTTGAGGATGCTCACTGCCACTGTGGTGTTGGTGGGAGCTGGAGGAGACTTGGGGTCCATCAAAGGAAAGAGGATGGGAGACAGGCAGGATACCTGCCATGGGTTCTATTCAGCTGCTAGACGCAATGGGTGAAATGTACACAGA... | GTCATGGGCGGGACGGGCTGCTGTTCAGTCCTTTACGGAAGTCTGTTCGGATGTGGCGGTGGGAAGGCCAGCTGGAGACAGGGGCCAAATCAGTGAGTGGGTGGTGAGAGAAAGTGATGGCGTAGTGAGGACAAAGCCTGGAGAAGGTCCCTAGGGAGGCCCACAACTGTGCTTACTTGAGGATGCTCACTGCCACTGTGGTGTTGGTGGGAGCTGGAGGAGACTTGGGGTCCATCAAAGGAAAGAGGATGGGAGACAGGCAGGATACCTGCCATGGGTTCTATTCAGCTGCTAGACGCAATGGGTGAAATGTACACAGA... |
Task1_train_44964 | This genomic variant is located on Chromosome 17. Can you determine its pathogenicity and name any linked disease? | Benign | AAAACTAGAGAGGGGTCTTGCACAGACGAATAATGTCAGTCCTGAATTGGGAAATGTGATTCACTTGCCCCTGCACCCTTGTGGTCCAAGAGGTGGGGACAGGAAAAAAAAGTACAGAAGAAAGAGTCAAAAAGCCCAAGTTCCAGTCTGGGGCCCGATACTAACTTGCTGTGAGACTATAGGTGAGTCCCTTCACCTCTCTGGCCTTCAGTGTTCATCTGAAAAGAAATCAATTCTCAGGTCTCTTTCCAGCACCACAATTTTATGAGCCATGATCAATAATCTTGGGTTTATCTGGTAAAGTAGTCAGTGAGAGCTTT... | AAAACTAGAGAGGGGTCTTGCACAGACGAATAATGTCAGTCCTGAATTGGGAAATGTGATTCACTTGCCCCTGCACCCTTGTGGTCCAAGAGGTGGGGACAGGAAAAAAAAGTACAGAAGAAAGAGTCAAAAAGCCCAAGTTCCAGTCTGGGGCCCGATACTAACTTGCTGTGAGACTATAGGTGAGTCCCTTCACCTCTCTGGCCTTCAGTGTTCATCTGAAAAGAAATCAATTCTCAGGTCTCTTTCCAGCACCACAATTTTATGAGCCATGATCAATAATCTTGGGTTTATCTGGTAAAGTAGTCAGTGAGAGCTTT... |
Task1_train_44965 | This alteration occurs on Chromosome 17. Is it associated with a disease or is it a benign variant? | Benign | ACCTCTCTGGCCTTCAGTGTTCATCTGAAAAGAAATCAATTCTCAGGTCTCTTTCCAGCACCACAATTTTATGAGCCATGATCAATAATCTTGGGTTTATCTGGTAAAGTAGTCAGTGAGAGCTTTAAGGAGTGGTAGGGCTTGAACTTTGAACAATGGGGGTTTGGGAGGGGCAAACAACATGAGGAGAGTTTTTAGGCAAATGAAACTTTGAAAGCAAAAAACTGTAAAAAGTTTAGCAGATGGCTATAAAATATCTATGGATGAAGCAGGCCTTCGCTCAGATCTCTGCCGGGACTCTCTAGTTGGGTCAGAAAATT... | ACCTCTCTGGCCTTCAGTGTTCATCTGAAAAGAAATCAATTCTCAGGTCTCTTTCCAGCACCACAATTTTATGAGCCATGATCAATAATCTTGGGTTTATCTGGTAAAGTAGTCAGTGAGAGCTTTAAGGAGTGGTAGGGCTTGAACTTTGAACAATGGGGGTTTGGGAGGGGCAAACAACATGAGGAGAGTTTTTAGGCAAATGAAACTTTGAAAGCAAAAAACTGTAAAAAGTTTAGCAGATGGCTATAAAATATCTATGGATGAAGCAGGCCTTCGCTCAGATCTCTGCCGGGACTCTCTAGTTGGGTCAGAAAATT... |
Task1_train_44966 | Here is a genetic alteration on Chromosome 17. Based on the data, is it a benign variant or a cause of disease? | Benign | AGTTGGAAGAATCAATGTTGTCAAAATGTTTATACTATCGAAAGCCATCTACAGATTCAGTGCAATCCTATCCAAATACCAATGACATTCTTCACAGAAATAGAACAAAGAATCTTAAATTTATATATATATATGTGTGTGTGTGTGTGTGTGTGTGTATATATATATATGGAACCACAAAAGATGCAGAATAGCTAAAGCTGTCCTGACCAAAAAGAACAAAACTGTAGAAACCACATTACCTGACTTCAAATTATATTACAGAGCTATAGTCACTAAAACAGCATGAGACTGACATAAAAACAGATTTTAAGCCCCTT... | AGTTGGAAGAATCAATGTTGTCAAAATGTTTATACTATCGAAAGCCATCTACAGATTCAGTGCAATCCTATCCAAATACCAATGACATTCTTCACAGAAATAGAACAAAGAATCTTAAATTTATATATATATATGTGTGTGTGTGTGTGTGTGTGTGTATATATATATATGGAACCACAAAAGATGCAGAATAGCTAAAGCTGTCCTGACCAAAAAGAACAAAACTGTAGAAACCACATTACCTGACTTCAAATTATATTACAGAGCTATAGTCACTAAAACAGCATGAGACTGACATAAAAACAGATTTTAAGCCCCTT... |
Task1_train_44967 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | CATTATCATTGTGCCCTATGACACCGTATGTGCAGCTAGACAGCCAGATTCAGGGAACAGCAAGGACAGGAAGAGTTCCAGACGATATAGTCCTTTCCTTACTTTACAGGTGGTCCTAAAGAAGGAGAGAAACTTTCCTGGCAGTGTTGCAACTAGAAGCTAGGTCTCCTGAGCCCCACACCGTCAGCTGTCCATGAGCACCGGGGAACCAAATGTTAGCAGAGTGTAGCAGCAGCTTCACACATGGGAGGGTGCTGAGATGGTAAGCCTCGTCCATGGAAAGTGTTCCTTCAATGTTAGCGGAATAAGGAACAAATGAG... | CATTATCATTGTGCCCTATGACACCGTATGTGCAGCTAGACAGCCAGATTCAGGGAACAGCAAGGACAGGAAGAGTTCCAGACGATATAGTCCTTTCCTTACTTTACAGGTGGTCCTAAAGAAGGAGAGAAACTTTCCTGGCAGTGTTGCAACTAGAAGCTAGGTCTCCTGAGCCCCACACCGTCAGCTGTCCATGAGCACCGGGGAACCAAATGTTAGCAGAGTGTAGCAGCAGCTTCACACATGGGAGGGTGCTGAGATGGTAAGCCTCGTCCATGGAAAGTGTTCCTTCAATGTTAGCGGAATAAGGAACAAATGAG... |
Task1_train_44968 | 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 | CAGGTGTCTCTAGACTGCACTATATGTGACAAATGGTGCTATCGAGTCCTCCTAAAGATTATTTATAGTTTATCTTGAGAACACATATGTAATGGGCTGTATCTGCTTGGCTAGATAAAAGTGAGACTTCCTTCTGTCTTTGCAGTCTCTTAGCAAACTGCCTGTGATGTGCTCACATTCTGGTTTAATGCTTATTCAATAATAAAACTGTTTTCTTTCTTCACTACTTTCGTGGAGAGGTTTTTTCTGGGTTGGGAGAAAATTTTGCTTCTAATTATATTCTCCCAACATAGCGCATGTGCTTAAAAGGGAAACAAAAG... | CAGGTGTCTCTAGACTGCACTATATGTGACAAATGGTGCTATCGAGTCCTCCTAAAGATTATTTATAGTTTATCTTGAGAACACATATGTAATGGGCTGTATCTGCTTGGCTAGATAAAAGTGAGACTTCCTTCTGTCTTTGCAGTCTCTTAGCAAACTGCCTGTGATGTGCTCACATTCTGGTTTAATGCTTATTCAATAATAAAACTGTTTTCTTTCTTCACTACTTTCGTGGAGAGGTTTTTTCTGGGTTGGGAGAAAATTTTGCTTCTAATTATATTCTCCCAACATAGCGCATGTGCTTAAAAGGGAAACAAAAG... |
Task1_train_44969 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | CATTGCCCCTTGGTGCAGTCCTGTGCTGGAAAAATACAGAAATAAAATATGTAGGGGAAGAAACTATGAGGAGCTCCCAGCAGGAAGGGGAAAATAGAATGGATCCCCAGCACACAGAGAGGGGCTGGAGATGTTAGCAGGAACAGTGACATTGCCTGGCCGCAGTGTTCTGGACTCCAGTGTTCATGGGCAGGGAGAAAAGTGAGGAAGTGCCATCAGGTGGGGAGAATCGGGGAGGCTTTCTAGAAAAAGAGAGCGGGGTTTGGAAGCAATGGACTGTACTGAGGACAAGCCTAGGCAAAATGTGTGCGTATGCATGT... | CATTGCCCCTTGGTGCAGTCCTGTGCTGGAAAAATACAGAAATAAAATATGTAGGGGAAGAAACTATGAGGAGCTCCCAGCAGGAAGGGGAAAATAGAATGGATCCCCAGCACACAGAGAGGGGCTGGAGATGTTAGCAGGAACAGTGACATTGCCTGGCCGCAGTGTTCTGGACTCCAGTGTTCATGGGCAGGGAGAAAAGTGAGGAAGTGCCATCAGGTGGGGAGAATCGGGGAGGCTTTCTAGAAAAAGAGAGCGGGGTTTGGAAGCAATGGACTGTACTGAGGACAAGCCTAGGCAAAATGTGTGCGTATGCATGT... |
Task1_train_44970 | This sequence variant lies on Chromosome 17. Is it clinically significant, and what condition might it cause if any? | Benign | TCCCAACACTTTGGGAGGCCGAGGCGGGTGGATCACGAGGTCGGGAGTTTGAGACCAGCCTGGCCAAGATGGTGAAACCCCGTCTCTCCTAAAAATACAAAAATTAGCCGGGTGTGTTGGCGTGTGCCTGTAGTTGCAGCTACTGGGAAGGCTGAGGCAGGAGAACTGCTTGAACCCAGGAGGCGGAGGTTGCTGTGAGCCAAGATCGCGCCACTGCACTCCAGCCTGGGCAACAGAGGGAGACTCTGTCTCAAAAAAAAAAAAAAAAAAAAAAAGAAGGAAAGAAAAGAAATTGAGAGAATGCTGAGGACACAGGGTAT... | TCCCAACACTTTGGGAGGCCGAGGCGGGTGGATCACGAGGTCGGGAGTTTGAGACCAGCCTGGCCAAGATGGTGAAACCCCGTCTCTCCTAAAAATACAAAAATTAGCCGGGTGTGTTGGCGTGTGCCTGTAGTTGCAGCTACTGGGAAGGCTGAGGCAGGAGAACTGCTTGAACCCAGGAGGCGGAGGTTGCTGTGAGCCAAGATCGCGCCACTGCACTCCAGCCTGGGCAACAGAGGGAGACTCTGTCTCAAAAAAAAAAAAAAAAAAAAAAAGAAGGAAAGAAAAGAAATTGAGAGAATGCTGAGGACACAGGGTAT... |
Task1_train_44971 | A mutation on Chromosome 17 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CTTGCACCAGCTGCTGGACTCGCAGGAGCATTTCAGAATGAACTGGGACACACACAGATGGGCAGTGGGGACAGTGGCCTAGGTGTGCCTTCTGCGTAGTGTGTTCCTGGAGCTCAGATACCCCTGCACAGGGCCAAGCCAGGGAATGTTCCTTCCCGCCCCCACCCACCCCCTACATCATGGCCAGGTACAGCCATCAAATCTGCTTTGGATTCCTCTGCCCCTGTTTCTCCAGCCTGCTCTCCAGAGAAAGCATGCTGCCTTTCTTTCTTTCTTTCTTTTTTTTTTTTTTTTTTTTGAGACGGAGTTTCACTCTTGCT... | CTTGCACCAGCTGCTGGACTCGCAGGAGCATTTCAGAATGAACTGGGACACACACAGATGGGCAGTGGGGACAGTGGCCTAGGTGTGCCTTCTGCGTAGTGTGTTCCTGGAGCTCAGATACCCCTGCACAGGGCCAAGCCAGGGAATGTTCCTTCCCGCCCCCACCCACCCCCTACATCATGGCCAGGTACAGCCATCAAATCTGCTTTGGATTCCTCTGCCCCTGTTTCTCCAGCCTGCTCTCCAGAGAAAGCATGCTGCCTTTCTTTCTTTCTTTCTTTTTTTTTTTTTTTTTTTTGAGACGGAGTTTCACTCTTGCT... |
Task1_train_44972 | A variant has been detected on Chromosome 17. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | AGCCTGGCTAAGACGGTGAAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCCGGGCATGGTGGCACGTGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGAGAATGGCGTGAACCCAGAAGGCGGAGCTTGCAGTGAGCCGAGATCGTGCCACTGCACTCCAGCTTGGGCGACAGAGCGAGACTCCATCTCAAAAAAAAAAAAAAAATGGATAAAATAAGCCTGATCCAGCCTCCCAGAGCAGGCCTTCCAAGGGCTTCCTCCTGCCTGTGGGAAGCGTGGCCTCACCTGCTCCTCCCAGGAGTTGATGACCA... | AGCCTGGCTAAGACGGTGAAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCCGGGCATGGTGGCACGTGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGAGAATGGCGTGAACCCAGAAGGCGGAGCTTGCAGTGAGCCGAGATCGTGCCACTGCACTCCAGCTTGGGCGACAGAGCGAGACTCCATCTCAAAAAAAAAAAAAAAATGGATAAAATAAGCCTGATCCAGCCTCCCAGAGCAGGCCTTCCAAGGGCTTCCTCCTGCCTGTGGGAAGCGTGGCCTCACCTGCTCCTCCCAGGAGTTGATGACCA... |
Task1_train_44973 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GCTAAGACGGTGAAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCCGGGCATGGTGGCACGTGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGAGAATGGCGTGAACCCAGAAGGCGGAGCTTGCAGTGAGCCGAGATCGTGCCACTGCACTCCAGCTTGGGCGACAGAGCGAGACTCCATCTCAAAAAAAAAAAAAAAATGGATAAAATAAGCCTGATCCAGCCTCCCAGAGCAGGCCTTCCAAGGGCTTCCTCCTGCCTGTGGGAAGCGTGGCCTCACCTGCTCCTCCCAGGAGTTGATGACCACCAGGT... | GCTAAGACGGTGAAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCCGGGCATGGTGGCACGTGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGAGAATGGCGTGAACCCAGAAGGCGGAGCTTGCAGTGAGCCGAGATCGTGCCACTGCACTCCAGCTTGGGCGACAGAGCGAGACTCCATCTCAAAAAAAAAAAAAAAATGGATAAAATAAGCCTGATCCAGCCTCCCAGAGCAGGCCTTCCAAGGGCTTCCTCCTGCCTGTGGGAAGCGTGGCCTCACCTGCTCCTCCCAGGAGTTGATGACCACCAGGT... |
Task1_train_44974 | A genomic variant on Chromosome 17 is under review. What is the biological outcome — benign or pathogenic? | Benign | GAGGCGGACAGGGCCTCTGCCTGTGGGGACACCGCCTGGTGGGAAGTCCAGCCAGCCCCCTACAGAGAGAGGAGATGCTACTGGTGTTCCTGAGTGGTCCTCGGGAGGGACCTCCTATCCCTCCTGTCCCCTGCCCTGCCCTGCCCAGCACCGGCCCTCCCTCGGTTGGCCAGCCTCAGGAATGAGGAGTCCCTCATTCCAGCCCAGCTAACCAATCCCCTTCCTAAGCTCCAAGCCCCTGCTCCTCCTGCCTCCATGGAACCCGGCTCCACCACCAGCACCCACACACCTGACACTCCTCCATTCCTGGCTCTTGCCCT... | GAGGCGGACAGGGCCTCTGCCTGTGGGGACACCGCCTGGTGGGAAGTCCAGCCAGCCCCCTACAGAGAGAGGAGATGCTACTGGTGTTCCTGAGTGGTCCTCGGGAGGGACCTCCTATCCCTCCTGTCCCCTGCCCTGCCCTGCCCAGCACCGGCCCTCCCTCGGTTGGCCAGCCTCAGGAATGAGGAGTCCCTCATTCCAGCCCAGCTAACCAATCCCCTTCCTAAGCTCCAAGCCCCTGCTCCTCCTGCCTCCATGGAACCCGGCTCCACCACCAGCACCCACACACCTGACACTCCTCCATTCCTGGCTCTTGCCCT... |
Task1_train_44975 | This is a variant located on Chromosome 17. Is this mutation a likely cause of disease or not? | Benign | GCTCCTGGGCAGATGGCTGTTGCAAGTCACCCTGGGGACGTGTGCAAAAGCCAAAGCAGGTGGACTGAATGTGGCCTTTGGGACTAATATGTATGCAACTGAGCTAAAGTTTTGGCTCCAGCAACCAAGTCCAACACAAAATAGGACATAGCCAGGCCTCCTTAGCCCTCAGGGCCTGAGGGGAAGTGGTGGCTGTAGCCTCTAATAGTCTAGTGGTCGTCATTCCTCCCTGGTGCATAAGGAGCGAAGGAGCAGTTTTTCCCCCAGTGACAACCTGTTGAACACACCTCTGCTTTCCCACACTGCCCTGACACAGTGGG... | GCTCCTGGGCAGATGGCTGTTGCAAGTCACCCTGGGGACGTGTGCAAAAGCCAAAGCAGGTGGACTGAATGTGGCCTTTGGGACTAATATGTATGCAACTGAGCTAAAGTTTTGGCTCCAGCAACCAAGTCCAACACAAAATAGGACATAGCCAGGCCTCCTTAGCCCTCAGGGCCTGAGGGGAAGTGGTGGCTGTAGCCTCTAATAGTCTAGTGGTCGTCATTCCTCCCTGGTGCATAAGGAGCGAAGGAGCAGTTTTTCCCCCAGTGACAACCTGTTGAACACACCTCTGCTTTCCCACACTGCCCTGACACAGTGGG... |
Task1_train_44976 | A genomic change on Chromosome 17 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TTTTCTTCAAAGGTACAAACCCTCTTCAGTGCATACCTAGGCCCCAAGCCACACCAGAACCAGGTTCTCCCTTCTAAACCCACAGGGCTCTCTCCCCCTAATCAAGATCTGCCCTTCTTTTCTCCCTGGGCCATGATGAGGTCCGAAAGAGCTCCAGTGTCCAGCCTTGCTATCTCGGGTTGCATATGCTGGGCATGTAGGGAATGCTCCAAGCATCTGCCAGAAGCGGGGTGGGGAAAGAAACCAGATTGGAAGGGAAGGGAGGACAAAAGGCTATGGGGTCAGTGCTGCCCAAAGGAGAGCAATTTTGGAAGTAACCT... | TTTTCTTCAAAGGTACAAACCCTCTTCAGTGCATACCTAGGCCCCAAGCCACACCAGAACCAGGTTCTCCCTTCTAAACCCACAGGGCTCTCTCCCCCTAATCAAGATCTGCCCTTCTTTTCTCCCTGGGCCATGATGAGGTCCGAAAGAGCTCCAGTGTCCAGCCTTGCTATCTCGGGTTGCATATGCTGGGCATGTAGGGAATGCTCCAAGCATCTGCCAGAAGCGGGGTGGGGAAAGAAACCAGATTGGAAGGGAAGGGAGGACAAAAGGCTATGGGGTCAGTGCTGCCCAAAGGAGAGCAATTTTGGAAGTAACCT... |
Task1_train_44977 | A genetic alteration is present on Chromosome 17. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GCGCTGTCCTCTGACAGGGACACCCAAACTTCAATGGTGGGCACAGCACCCACCTTGAACTCCCTCCCACAATTAAAGAGGCCCATCGTAAAAGCATCTGCTTTAGTCTTCAATAAATCCAGATACCTACACTCACACTATGAAATAAATTTTCACAGCCTTTTTGGAGGAATTCTCTTAATGGGAACCGCAGGCGTTTCTCCTTCACACCCAGGGCTTTCCCAAGTTCCCGTCCTTGTTTGTAACGTATGCCCTCCCACCCACCTCCACCCTTGACACACAAGTCTGTCTCTTCCTTGTTATAGGACCAAACACACACC... | GCGCTGTCCTCTGACAGGGACACCCAAACTTCAATGGTGGGCACAGCACCCACCTTGAACTCCCTCCCACAATTAAAGAGGCCCATCGTAAAAGCATCTGCTTTAGTCTTCAATAAATCCAGATACCTACACTCACACTATGAAATAAATTTTCACAGCCTTTTTGGAGGAATTCTCTTAATGGGAACCGCAGGCGTTTCTCCTTCACACCCAGGGCTTTCCCAAGTTCCCGTCCTTGTTTGTAACGTATGCCCTCCCACCCACCTCCACCCTTGACACACAAGTCTGTCTCTTCCTTGTTATAGGACCAAACACACACC... |
Task1_train_44978 | Here is a variant on Chromosome 17. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CTGGGAGGCGGAGGTTGCAGTGAGCTAAGATCACGCCACTGTACTCCAGCCTGGGCAACAAAGCCAGACCCTGTCTCAAAAAAAAAAAAAAAAGTTGAGGGCAGGAGCTGAAAGCAGTCAGTTAAATAGGTGATTGGGGGCTGAGGATGTGAGGTCCTGGAGTCTGTCTAGTTTCTTCAGTAAGATGAAAAAAACTCTTTTCTTTTTTCTCTCCAGACTCAGTGGTTCTCCATCCTTCCGGACTTCAGCCTGGATCTCCAAGAGGGGCCCTCTGTAGAGTCCCAGCCCTACTCCGATCCTCATATACCCCCGGTATCTAA... | CTGGGAGGCGGAGGTTGCAGTGAGCTAAGATCACGCCACTGTACTCCAGCCTGGGCAACAAAGCCAGACCCTGTCTCAAAAAAAAAAAAAAAAGTTGAGGGCAGGAGCTGAAAGCAGTCAGTTAAATAGGTGATTGGGGGCTGAGGATGTGAGGTCCTGGAGTCTGTCTAGTTTCTTCAGTAAGATGAAAAAAACTCTTTTCTTTTTTCTCTCCAGACTCAGTGGTTCTCCATCCTTCCGGACTTCAGCCTGGATCTCCAAGAGGGGCCCTCTGTAGAGTCCCAGCCCTACTCCGATCCTCATATACCCCCGGTATCTAA... |
Task1_train_44979 | With a mutation on Chromosome 17, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TGCCAAACCTGGACTTCACAAGGAAAGGGCAGGCTGGGGAGGCAAAGGCACCTTGAGGAACCTCAGACAGCTCTGCCCCTGCCGGGACTCCACCTTCCACCCCAGGCTAGCCTTACAACCTGCCAGCGCTGGGTGCAACTGTCCCTGGCCAACACCCCCTCCCCCAACCCCCATCAGGGTTGGAAAATTCCAGTCTTCTTCCTTCTATAGTCAAGGAGGCAGAAAGTGCAGATGGGGCCAGAGGGGCAGAACAAGTTTGAGAAGGGAACAATGTGTCAGGAACTTGCTCTAAACAGCTGCCAAACTTTATTCTCATCCTC... | TGCCAAACCTGGACTTCACAAGGAAAGGGCAGGCTGGGGAGGCAAAGGCACCTTGAGGAACCTCAGACAGCTCTGCCCCTGCCGGGACTCCACCTTCCACCCCAGGCTAGCCTTACAACCTGCCAGCGCTGGGTGCAACTGTCCCTGGCCAACACCCCCTCCCCCAACCCCCATCAGGGTTGGAAAATTCCAGTCTTCTTCCTTCTATAGTCAAGGAGGCAGAAAGTGCAGATGGGGCCAGAGGGGCAGAACAAGTTTGAGAAGGGAACAATGTGTCAGGAACTTGCTCTAAACAGCTGCCAAACTTTATTCTCATCCTC... |
Task1_train_44980 | This variant lies on Chromosome 17. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CCCCAACCCCCATCAGGGTTGGAAAATTCCAGTCTTCTTCCTTCTATAGTCAAGGAGGCAGAAAGTGCAGATGGGGCCAGAGGGGCAGAACAAGTTTGAGAAGGGAACAATGTGTCAGGAACTTGCTCTAAACAGCTGCCAAACTTTATTCTCATCCTCAGCCTGGAGGTGAATCCCAGAGTCAGGACCACTCTCAACACGCGTGGGACCAAGGGTGAGAGAGAAGAAAACATTCACCCATTCTCTATCATAAGAACCCCAGTGGGTGGGGGGAGGGGAGAAAGGAAAAGTTTTCCTGGAGGCACTCTGCCCCCGACCCA... | CCCCAACCCCCATCAGGGTTGGAAAATTCCAGTCTTCTTCCTTCTATAGTCAAGGAGGCAGAAAGTGCAGATGGGGCCAGAGGGGCAGAACAAGTTTGAGAAGGGAACAATGTGTCAGGAACTTGCTCTAAACAGCTGCCAAACTTTATTCTCATCCTCAGCCTGGAGGTGAATCCCAGAGTCAGGACCACTCTCAACACGCGTGGGACCAAGGGTGAGAGAGAAGAAAACATTCACCCATTCTCTATCATAAGAACCCCAGTGGGTGGGGGGAGGGGAGAAAGGAAAAGTTTTCCTGGAGGCACTCTGCCCCCGACCCA... |
Task1_train_44981 | 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 | TCCGGCCTGGCGCAGTCTCTGAGGAGGGGGCGGCCGCGGCACCGGAAGTGCCCCCCACGGGAGGCTGCCCTCGGGGTCGCAGGCCGCATGGCCAAGCGTGGACCGGGGCCGCATGGCAGCGCGGGGACCCCTCCCCCCAGGTCCCGGCCACCGGAAGCCCGGAACGGCCACATGGTCGGCAGGAGCCGGCAGCCCCTAGCGCGGGGAGCTAGTCCTCGCGGGGGTTCCGAGGGGGCCTGAGATTTTGAGGAGTGGAAGCCGGAGGCTCGGGTCCTAATCACCCCGGAGGGCCTGCTGCAGGCATATGTTAGCGCTTCCCA... | TCCGGCCTGGCGCAGTCTCTGAGGAGGGGGCGGCCGCGGCACCGGAAGTGCCCCCCACGGGAGGCTGCCCTCGGGGTCGCAGGCCGCATGGCCAAGCGTGGACCGGGGCCGCATGGCAGCGCGGGGACCCCTCCCCCCAGGTCCCGGCCACCGGAAGCCCGGAACGGCCACATGGTCGGCAGGAGCCGGCAGCCCCTAGCGCGGGGAGCTAGTCCTCGCGGGGGTTCCGAGGGGGCCTGAGATTTTGAGGAGTGGAAGCCGGAGGCTCGGGTCCTAATCACCCCGGAGGGCCTGCTGCAGGCATATGTTAGCGCTTCCCA... |
Task1_train_44982 | Here is a variant on Chromosome 17. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GCCGGGCGTAGTGTCATATGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGAAGAATCGCTTGAACCCGGGAGGTGGAGGTTGCGGTGAGCCGAGATCATACCATTGCACTCTAGCCTGGGCGACAAGAGCTAAACTCCGTCTCAAAAAAAACAAAAAAACAAAAAAACAAAAAAAAAACATGCTGTTTGAGCCTTGACCTTGCTGTTGCCTCTGTAAGGATCTCTAAGGATTCTTATTCCTAGGACTTCCTTCACCTAGCTAGTTTTCTTTTCCTTTCTTTTTTTTTATTGAGACGGAGTCTCGCTCTGTTGCCCA... | GCCGGGCGTAGTGTCATATGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGAAGAATCGCTTGAACCCGGGAGGTGGAGGTTGCGGTGAGCCGAGATCATACCATTGCACTCTAGCCTGGGCGACAAGAGCTAAACTCCGTCTCAAAAAAAACAAAAAAACAAAAAAACAAAAAAAAAACATGCTGTTTGAGCCTTGACCTTGCTGTTGCCTCTGTAAGGATCTCTAAGGATTCTTATTCCTAGGACTTCCTTCACCTAGCTAGTTTTCTTTTCCTTTCTTTTTTTTTATTGAGACGGAGTCTCGCTCTGTTGCCCA... |
Task1_train_44983 | Here is a genetic alteration on Chromosome 17. Based on the data, is it a benign variant or a cause of disease? | Benign | GGCAGGAAGGTACGGGGGTGTGGGAGTGGACAGGGAGAATGAGGGGAGAAAGTCAAACACAGGGAGGCCAAGCACCAAAGAGAAGCAGGAGGATGAGGTACAGCCCCCAGTCCCAGCCCCACCGAAAGCCCCGGCCCAGAGGCTCTCTCTGGGCGGCCCTTACCCTGATCGATACCATTAATGAAGAAGTGTAGGGCAGAGTTGGACTTCCTTGTGAGGCCAATGTGGTCACCCTCCTAATCAAAGAAGACAAACAGTTTAGAGGAGTCCTGAGGCCTGCTCAGCACCCCACTCCACACAGGAACAACTCCAGAAGGTAT... | GGCAGGAAGGTACGGGGGTGTGGGAGTGGACAGGGAGAATGAGGGGAGAAAGTCAAACACAGGGAGGCCAAGCACCAAAGAGAAGCAGGAGGATGAGGTACAGCCCCCAGTCCCAGCCCCACCGAAAGCCCCGGCCCAGAGGCTCTCTCTGGGCGGCCCTTACCCTGATCGATACCATTAATGAAGAAGTGTAGGGCAGAGTTGGACTTCCTTGTGAGGCCAATGTGGTCACCCTCCTAATCAAAGAAGACAAACAGTTTAGAGGAGTCCTGAGGCCTGCTCAGCACCCCACTCCACACAGGAACAACTCCAGAAGGTAT... |
Task1_train_44984 | The following genetic variant occurs on Chromosome 17. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CAGACTCGGAGCTGCTTCCCCCTAACAGAACCAAATCCCCCGAACAGAGCCCCCCTCTGAGGACCTGGGAAGCCTGCACCCTGGGGCCCTACTGTTTCGAGCGTCTGGGCATCCTCCATCTCTTCCCACCATGGCTGATGCCCTTGCCCATGGAGCTGATGTCAACTGGGTCAATGGGGGCCAAGATAATGCCACACCGCTGATCCAGGCCACAGCTGCTGTAAGAGCCCTGCTGACCTCTCCACCCCACCCTAGGGCTCTGACACCTACTCCTGACTCTGGGCCCTGCCCTTACCTCCTTTCCCCACCACCTGTTCCCT... | CAGACTCGGAGCTGCTTCCCCCTAACAGAACCAAATCCCCCGAACAGAGCCCCCCTCTGAGGACCTGGGAAGCCTGCACCCTGGGGCCCTACTGTTTCGAGCGTCTGGGCATCCTCCATCTCTTCCCACCATGGCTGATGCCCTTGCCCATGGAGCTGATGTCAACTGGGTCAATGGGGGCCAAGATAATGCCACACCGCTGATCCAGGCCACAGCTGCTGTAAGAGCCCTGCTGACCTCTCCACCCCACCCTAGGGCTCTGACACCTACTCCTGACTCTGGGCCCTGCCCTTACCTCCTTTCCCCACCACCTGTTCCCT... |
Task1_train_44985 | Chromosome 17 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GCTCCTTGAACCCTGATCTTCTGTCTCATCTCCTCTCCCCACTGGGTCCTGAAAGCTCCAGCATGGTCCTGGCCTCCCTGCTGGAGCCACTGCTGGCCCATAGAGCCTTATTGCATTAGGGAAAAGGCTTCCCTTCCTCCAGGCAGATGCGGCTCCAAGGCACATAGCCTAGTGAGCTGACTGTGGGCCAGGGCCCAGCCCTAACTCTTGCCCTTATTCCCATCCTATTTACCAGCTCCTCTTTCCACAGCCCCGACTCCACAATCTGGAAGGGCCAGAATGGTCGCACCTTCAAAGTGGGCAGCTTCCCAGCCTCGGCA... | GCTCCTTGAACCCTGATCTTCTGTCTCATCTCCTCTCCCCACTGGGTCCTGAAAGCTCCAGCATGGTCCTGGCCTCCCTGCTGGAGCCACTGCTGGCCCATAGAGCCTTATTGCATTAGGGAAAAGGCTTCCCTTCCTCCAGGCAGATGCGGCTCCAAGGCACATAGCCTAGTGAGCTGACTGTGGGCCAGGGCCCAGCCCTAACTCTTGCCCTTATTCCCATCCTATTTACCAGCTCCTCTTTCCACAGCCCCGACTCCACAATCTGGAAGGGCCAGAATGGTCGCACCTTCAAAGTGGGCAGCTTCCCAGCCTCGGCA... |
Task1_train_44986 | This variant lies on Chromosome 17. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CCGGGAGGCGGAGGCTGCAGCCAGCCGAGTTCAAGTTGTTTCCTTCTCAACTGTGCAGGCATTTCCAGGAGTCTGGAGTCAGTTCTGTCCCTCGGTCCTCGTCCCACAGGGGGTGGTTCAAGCCCCCCTGAAATTCGACAAGCCAGAGCTGTGCCCCAGGGACCTCCAGGCCTGCCTCCACGCCCACCTTTATCCTCTAGCTCTCCTCAGCCCAGCCAGCCCTCTAGGGAGAGGCTTCCCTGGCCCAAAAGAAAACCCCCACACAATCACCCCATGGGAATGCCTGGAGCCCGTAAAGCCGCTGCCCTCTCTGGAGGCCT... | CCGGGAGGCGGAGGCTGCAGCCAGCCGAGTTCAAGTTGTTTCCTTCTCAACTGTGCAGGCATTTCCAGGAGTCTGGAGTCAGTTCTGTCCCTCGGTCCTCGTCCCACAGGGGGTGGTTCAAGCCCCCCTGAAATTCGACAAGCCAGAGCTGTGCCCCAGGGACCTCCAGGCCTGCCTCCACGCCCACCTTTATCCTCTAGCTCTCCTCAGCCCAGCCAGCCCTCTAGGGAGAGGCTTCCCTGGCCCAAAAGAAAACCCCCACACAATCACCCCATGGGAATGCCTGGAGCCCGTAAAGCCGCTGCCCTCTCTGGAGGCCT... |
Task1_train_44987 | Given this variant on Chromosome 17, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CATTTTGTGGGGTGTTAGTGCCAAACTTGAATAGGGGCTGGGGTGCTGTCTTCCACTGACACCCAAATCCAGAATCCCTGGTCTTGAGTCCCCAGAACTTTGCCTCTTGACTGTCCCTTCTCTTCCTACCTCCATCCATGGAAAATTAGTTATTTTCTGATCCTTTCCCCTGCCTGGTCTAGCTCCTCTCCAAACAGCCATGCCCTCCAAATGCTAGAGACCTGGGCCCTGAACCCTGTAGACAGATGCCCTCAGAATTGGGGCATGGGAGGGGGGCTGGGGGACCCCATGATTCAGCCACGGACTCCAATGCCCAGCTC... | CATTTTGTGGGGTGTTAGTGCCAAACTTGAATAGGGGCTGGGGTGCTGTCTTCCACTGACACCCAAATCCAGAATCCCTGGTCTTGAGTCCCCAGAACTTTGCCTCTTGACTGTCCCTTCTCTTCCTACCTCCATCCATGGAAAATTAGTTATTTTCTGATCCTTTCCCCTGCCTGGTCTAGCTCCTCTCCAAACAGCCATGCCCTCCAAATGCTAGAGACCTGGGCCCTGAACCCTGTAGACAGATGCCCTCAGAATTGGGGCATGGGAGGGGGGCTGGGGGACCCCATGATTCAGCCACGGACTCCAATGCCCAGCTC... |
Task1_train_44988 | A genomic change on Chromosome 17 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TCACCATGTGAACTCAGAAACTGAGAAACAGAGAAACTCAGGCCCTGCCTTTCTGCTACACAATTGGGATCATATGCACATGCACACACATACCACTTGAGAACAAGCAGCTGTGTGCGTGAGCCCAGGCTGAGGGAGCTGGACTTCACCTTCCACTCTAGACAGATTCCTGGAATGTGAGCAGACGGACCGTTTACAAATGGCCCTACTTCTCTCATTCAACTAACGTTACTGATCATTTTCAATGGATTCCATTCAGTGGAATCTGAATCTACTCTGCATCTACTCTGTGTTTGGAGGCTGGATGGGATATGATCACT... | TCACCATGTGAACTCAGAAACTGAGAAACAGAGAAACTCAGGCCCTGCCTTTCTGCTACACAATTGGGATCATATGCACATGCACACACATACCACTTGAGAACAAGCAGCTGTGTGCGTGAGCCCAGGCTGAGGGAGCTGGACTTCACCTTCCACTCTAGACAGATTCCTGGAATGTGAGCAGACGGACCGTTTACAAATGGCCCTACTTCTCTCATTCAACTAACGTTACTGATCATTTTCAATGGATTCCATTCAGTGGAATCTGAATCTACTCTGCATCTACTCTGTGTTTGGAGGCTGGATGGGATATGATCACT... |
Task1_train_44989 | A genomic variant on Chromosome 17 is under review. What is the biological outcome — benign or pathogenic? | Benign | TGTTGGGTTGTTTGTTTGTTTTGAGACAGTCTCACTCTGTCACCCAGGCCGGACTTCTGTGGCGCGATCTTGGCTCGCTGCAACCTCCACCTCTCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCGCCCACCAACATGCCCAGCTAATTTTTGTGTTTTTAGTAGAGGTTTCGCCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGGTGGTCCACCTGCCTGGGATTATAGGCGTGAGCCACTGCGCCCAGCAAGTTTCCTTCCTTCCTTCCTTCCTTCCTTCCTTCCTTCCT... | TGTTGGGTTGTTTGTTTGTTTTGAGACAGTCTCACTCTGTCACCCAGGCCGGACTTCTGTGGCGCGATCTTGGCTCGCTGCAACCTCCACCTCTCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCGCCCACCAACATGCCCAGCTAATTTTTGTGTTTTTAGTAGAGGTTTCGCCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGGTGGTCCACCTGCCTGGGATTATAGGCGTGAGCCACTGCGCCCAGCAAGTTTCCTTCCTTCCTTCCTTCCTTCCTTCCTTCCTTCCT... |
Task1_train_44990 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | AGGAAACACTGTGGTGGTCTGTAGCGTGGGAGTGCCACTCCTTCGGCCAGCCTGGGTCCCTGCCCTTGGCTTCCTGAAATGAGAAACCAGTGTCCCCTTCTTGGTGTGAGGCACCCCTTGGCTTAGTGGCCACGCGGCTGCCAGCAGGCCCTCCTAGTCTGCACCATGCACTACGTAGCTCTTGCACTGGCTGACGACAACCACCCAGGCTCTTTATTCTCCCTGTTTCCAGCAAGGATCAGGTCTGGATTCTGAACTCAGTGTCTTGAGTGGAGCTCTTTGGGATTTACTTAGCACATGGTACAGGACCAGGCCAAGGC... | AGGAAACACTGTGGTGGTCTGTAGCGTGGGAGTGCCACTCCTTCGGCCAGCCTGGGTCCCTGCCCTTGGCTTCCTGAAATGAGAAACCAGTGTCCCCTTCTTGGTGTGAGGCACCCCTTGGCTTAGTGGCCACGCGGCTGCCAGCAGGCCCTCCTAGTCTGCACCATGCACTACGTAGCTCTTGCACTGGCTGACGACAACCACCCAGGCTCTTTATTCTCCCTGTTTCCAGCAAGGATCAGGTCTGGATTCTGAACTCAGTGTCTTGAGTGGAGCTCTTTGGGATTTACTTAGCACATGGTACAGGACCAGGCCAAGGC... |
Task1_train_44991 | A change on Chromosome 17 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GCCACGCGGCTGCCAGCAGGCCCTCCTAGTCTGCACCATGCACTACGTAGCTCTTGCACTGGCTGACGACAACCACCCAGGCTCTTTATTCTCCCTGTTTCCAGCAAGGATCAGGTCTGGATTCTGAACTCAGTGTCTTGAGTGGAGCTCTTTGGGATTTACTTAGCACATGGTACAGGACCAGGCCAAGGCTCTGGATTCCAGCCATGCCTTCCCCAAGGCTCTGAGGCGGAGGTCTCCCCAGTCTCTGGTGTGGTCAAGAGGTAAAGGATTCAGGATTCTGAAATGAAACTGCAGGAGTGGCCGAGTGCGGTGGCTCA... | GCCACGCGGCTGCCAGCAGGCCCTCCTAGTCTGCACCATGCACTACGTAGCTCTTGCACTGGCTGACGACAACCACCCAGGCTCTTTATTCTCCCTGTTTCCAGCAAGGATCAGGTCTGGATTCTGAACTCAGTGTCTTGAGTGGAGCTCTTTGGGATTTACTTAGCACATGGTACAGGACCAGGCCAAGGCTCTGGATTCCAGCCATGCCTTCCCCAAGGCTCTGAGGCGGAGGTCTCCCCAGTCTCTGGTGTGGTCAAGAGGTAAAGGATTCAGGATTCTGAAATGAAACTGCAGGAGTGGCCGAGTGCGGTGGCTCA... |
Task1_train_44992 | Chromosome 17 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AGCTTCCTGCAGGATCCATACTGGGCTACCTGGAGTTGAGGAATATGGAATGGAAGAACTCAGATGATGCCAAAGATAAGTTCCCCCAGACCAAGACTTCCCCTTACTGCAGCTTCCATCCTTGCAGTTCTGAGAAGAACACAGACTCCCAGGCTCCATTCTACCCCAAATTCCTTGCCTACTCCCGGGATACTGCATGTGCCAAGACTTGCTTTCATTCTGCAACCACTGCCCAGAGCTCAGTGTGCACCCTTCCTCCACCGTTCACTCTTTCCCTGCCTCTCGTTCCTCCCAGATCCTTTGTCCCTCCTCAACCCACC... | AGCTTCCTGCAGGATCCATACTGGGCTACCTGGAGTTGAGGAATATGGAATGGAAGAACTCAGATGATGCCAAAGATAAGTTCCCCCAGACCAAGACTTCCCCTTACTGCAGCTTCCATCCTTGCAGTTCTGAGAAGAACACAGACTCCCAGGCTCCATTCTACCCCAAATTCCTTGCCTACTCCCGGGATACTGCATGTGCCAAGACTTGCTTTCATTCTGCAACCACTGCCCAGAGCTCAGTGTGCACCCTTCCTCCACCGTTCACTCTTTCCCTGCCTCTCGTTCCTCCCAGATCCTTTGTCCCTCCTCAACCCACC... |
Task1_train_44993 | A mutation on Chromosome 17 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CCAGGTCCCACTAGGTGCTCTACCCTGAGGGAGCCTAGGGGCTGACTGTGACTTCCGAGGCTGCTGAGACCCTTAGATCTTTGGGCCTAGGAGGGAGTCAGAGAGGGGGATGTCTGAAGATGGTCCTGGCTGATCACTTCTTTCTTTCCACACTCACACAACGCCATGCCTTTTCCTGAGATGGCGCTGGGAGTTCCCACATGGACAGCCAGGGCATAAACACTTCCCACCCCGGCTCAGCCAGTTCCTGGAGTCCTGTGCCCCTTTTCATTGCCACTGAGCCATTTCTAGATTCACTGGAGCTCAGGATTCATGTGTCC... | CCAGGTCCCACTAGGTGCTCTACCCTGAGGGAGCCTAGGGGCTGACTGTGACTTCCGAGGCTGCTGAGACCCTTAGATCTTTGGGCCTAGGAGGGAGTCAGAGAGGGGGATGTCTGAAGATGGTCCTGGCTGATCACTTCTTTCTTTCCACACTCACACAACGCCATGCCTTTTCCTGAGATGGCGCTGGGAGTTCCCACATGGACAGCCAGGGCATAAACACTTCCCACCCCGGCTCAGCCAGTTCCTGGAGTCCTGTGCCCCTTTTCATTGCCACTGAGCCATTTCTAGATTCACTGGAGCTCAGGATTCATGTGTCC... |
Task1_train_44994 | This alteration occurs on Chromosome 17. Is it associated with a disease or is it a benign variant? | Benign | GGGGCAACCCTCCCCCAAACCTCCTTGACCTGGCTTGGGAGAGGCCATCTCCGAAGTCCAGGAATATGGGGAGGAACATGGAAGATCCAAAGGCATGGAAGCTGAGGAAGGTGTCTTGATACAAGGGAAACAGGGACGTAGAGACCCACGCTGGGGAAGGATGAAACCCAAAGCCACACTCCCAGGTGGGCGGGGTCAGGTATCACAATGGTCTGGTCCAGGCCCTGGGCCACAAAGAATGGAATGTGCTAGGAAGCAACTGGGAAGGGCTTAGAGAAAGCTTCAGAACAAGGCGGGTCATTAGGTGAGAGAGATGGTTT... | GGGGCAACCCTCCCCCAAACCTCCTTGACCTGGCTTGGGAGAGGCCATCTCCGAAGTCCAGGAATATGGGGAGGAACATGGAAGATCCAAAGGCATGGAAGCTGAGGAAGGTGTCTTGATACAAGGGAAACAGGGACGTAGAGACCCACGCTGGGGAAGGATGAAACCCAAAGCCACACTCCCAGGTGGGCGGGGTCAGGTATCACAATGGTCTGGTCCAGGCCCTGGGCCACAAAGAATGGAATGTGCTAGGAAGCAACTGGGAAGGGCTTAGAGAAAGCTTCAGAACAAGGCGGGTCATTAGGTGAGAGAGATGGTTT... |
Task1_train_44995 | This mutation is located on Chromosome 17. Is it associated with a disease or is it a benign polymorphism? | Benign | AGGAATGCGCAGGAAAGCTCAGCAGGCCGCGGAAAAAGAAGGCCCTGGCCCTGCATACGGGGCACACACGAACGACCACCAGCGCAAATGAACACATGAAGCTGGCTGGGTACTTTGTCCCCACCAGCAGATAGATCCACATCTGTATACTTGAACATAAATGCAGAGGCCTTGGTGTCGGCCTCTGGGGACAGCATCAACAAAACACCAGGTGGAAGCACACACAGAAAAAACACATTCCTGAAACTCCACAGGGACAATCCCAAGAACTCCTCCCTGGTGCTGGAAAATTAAAAACTAAGGAGATGGAGGAGCCAGGG... | AGGAATGCGCAGGAAAGCTCAGCAGGCCGCGGAAAAAGAAGGCCCTGGCCCTGCATACGGGGCACACACGAACGACCACCAGCGCAAATGAACACATGAAGCTGGCTGGGTACTTTGTCCCCACCAGCAGATAGATCCACATCTGTATACTTGAACATAAATGCAGAGGCCTTGGTGTCGGCCTCTGGGGACAGCATCAACAAAACACCAGGTGGAAGCACACACAGAAAAAACACATTCCTGAAACTCCACAGGGACAATCCCAAGAACTCCTCCCTGGTGCTGGAAAATTAAAAACTAAGGAGATGGAGGAGCCAGGG... |
Task1_train_44996 | Here is a variant on Chromosome 17. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TGGGAGGCGGGGGGTGGTGGGGTGGATCACTTGAGGTAAGGAGTTCAAGACCAGCATGGCCAACATGGAGAAACCCCATCTCTACGAAAAATAAAAAATTAGCGGGGTGTGGTGGCACATGCCTGTAATCCCAGGTACTTGGGAGGATGAGGTAGGAGAATTGCTTGAACCCAGGAGGTGGAGGTTGCGGTGAGCCGAGATTGCACGCACCACTGCACTCCAGCCTGGGCAAGAAGAGCAAAACTCCGTCCCAAAAAAAAAAAAAAAAATTAGCCAGGTGTAGTGGCACATTCTTGTAATCCCAGCTACTTGGGAGGCTG... | TGGGAGGCGGGGGGTGGTGGGGTGGATCACTTGAGGTAAGGAGTTCAAGACCAGCATGGCCAACATGGAGAAACCCCATCTCTACGAAAAATAAAAAATTAGCGGGGTGTGGTGGCACATGCCTGTAATCCCAGGTACTTGGGAGGATGAGGTAGGAGAATTGCTTGAACCCAGGAGGTGGAGGTTGCGGTGAGCCGAGATTGCACGCACCACTGCACTCCAGCCTGGGCAAGAAGAGCAAAACTCCGTCCCAAAAAAAAAAAAAAAAATTAGCCAGGTGTAGTGGCACATTCTTGTAATCCCAGCTACTTGGGAGGCTG... |
Task1_train_44997 | A variant was discovered on Chromosome 17. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GTGATCTCGACTCCCCCCTGGCCACAGACCCCCAGGGCATTGTGTTCACTGTACTCTGTGGGCAAGGATGGGTCCAGAAGACCCCACTTCAGGCACTAAGAGGGGCTGGACCTGGCGGCAGGAAGCCAAAGAGACTGGGCCTAGGCCAGGAGTTCCCAAATGTGAGGGGCGAGAAACAAGACAAGCTCCTCCCTTGAGAATTCCCTGTGGATTTTTAAAACAGATATTATTTTTATTATTATTGTGACAAAATGTTGATAAATGGATATTAAATAGAATAAGTCATAGTCTCTCTCTTTATTGGGGCTCAGGGGACACTC... | GTGATCTCGACTCCCCCCTGGCCACAGACCCCCAGGGCATTGTGTTCACTGTACTCTGTGGGCAAGGATGGGTCCAGAAGACCCCACTTCAGGCACTAAGAGGGGCTGGACCTGGCGGCAGGAAGCCAAAGAGACTGGGCCTAGGCCAGGAGTTCCCAAATGTGAGGGGCGAGAAACAAGACAAGCTCCTCCCTTGAGAATTCCCTGTGGATTTTTAAAACAGATATTATTTTTATTATTATTGTGACAAAATGTTGATAAATGGATATTAAATAGAATAAGTCATAGTCTCTCTCTTTATTGGGGCTCAGGGGACACTC... |
Task1_train_44998 | This mutation on Chromosome 17 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TTGACTTTGCCCTGATGAAGCAGGGCCAACAGTCCCCTAACTTAATTACAAAAACTAATGACTAAGAGAGAGGTGGCTAGAGCTGAGGCCCCTGAGTCAGGCTGTGGGTGGGATCATCTCCAGTACAGGAAGTGAGACTTTCATTTCCTCCTTTCCAAGAGAGGGCTGAGGGAGCAGGGTTGAGCAACTGGTGCAGACAGCCTAGCTGGACTTTGGGTGAGGCGGTTCAGCCATGAGGCTGGCTGTGCTTTTCTCGGGGGCCCTGCTGGGGCTACTGGCAGGTAAGGAGGAAGGAGGCTGAGGGGAGGGGGCCCCTGGGA... | TTGACTTTGCCCTGATGAAGCAGGGCCAACAGTCCCCTAACTTAATTACAAAAACTAATGACTAAGAGAGAGGTGGCTAGAGCTGAGGCCCCTGAGTCAGGCTGTGGGTGGGATCATCTCCAGTACAGGAAGTGAGACTTTCATTTCCTCCTTTCCAAGAGAGGGCTGAGGGAGCAGGGTTGAGCAACTGGTGCAGACAGCCTAGCTGGACTTTGGGTGAGGCGGTTCAGCCATGAGGCTGGCTGTGCTTTTCTCGGGGGCCCTGCTGGGGCTACTGGCAGGTAAGGAGGAAGGAGGCTGAGGGGAGGGGGCCCCTGGGA... |
Task1_train_44999 | Here’s a variant located on Chromosome 17. What is the predicted biological effect — harmless or disease-causing? | Benign | GGCCTAATTTTGTAGAGATGTGGTCTTGCCCATGTTGCCTAGGCTGGTCTTGAACTCCTGGGCTCAAGTGATCCTCCACCCTCAACCTCTCAAAGTGTTGAGATTTTTGTTGTTGCTGTTTTGTTTTTGTTTTTGAGACTGGGTATGGCTCTGTCACTCAGGCTGGAGTCCAGTGGCATGATCTCGGCTCACTGCAACCTCCACTTCCTGGGATCAAGCGATTCTCATGCCTCAGCCTCCCCAGTAGCTGGGCCTAGAGGAGCATGCCATTGCGTGCTGGCTTTTTTTGTATTGTTTGTAGAGACGAGACTTTGCTTTCC... | GGCCTAATTTTGTAGAGATGTGGTCTTGCCCATGTTGCCTAGGCTGGTCTTGAACTCCTGGGCTCAAGTGATCCTCCACCCTCAACCTCTCAAAGTGTTGAGATTTTTGTTGTTGCTGTTTTGTTTTTGTTTTTGAGACTGGGTATGGCTCTGTCACTCAGGCTGGAGTCCAGTGGCATGATCTCGGCTCACTGCAACCTCCACTTCCTGGGATCAAGCGATTCTCATGCCTCAGCCTCCCCAGTAGCTGGGCCTAGAGGAGCATGCCATTGCGTGCTGGCTTTTTTTGTATTGTTTGTAGAGACGAGACTTTGCTTTCC... |
Subsets and Splits
No community queries yet
The top public SQL queries from the community will appear here once available.