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_34700 | With a mutation on Chromosome 2, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GGTGACAGCAGATTTAGAGGAGCACAGGCCATCCCCGCTTAGGGGGTGGAAAATCAAGGTGGTGTGGTCAAAGGAAAATGGGAAATAGGCCTGAGAAAACCAGCCAATCGGCCCAGGGCCCAGGTGGGAAGTCAGAACACCTAACCCATCAGAACTGGAAGTGATCACAGCACCCATCTTGCCCCATCTTCCTGAGGGGGGGATGCCAGTGCCCAGAACCACACCCTGGCCTCCCGCCCAGGCTGGCACCCACTTTGTTTCACCTGCTGGTTTGAGTCCTCACTCGAGTTCTGCTCCTGGTGTGTCCAAGGCCTCCCACC... | GGTGACAGCAGATTTAGAGGAGCACAGGCCATCCCCGCTTAGGGGGTGGAAAATCAAGGTGGTGTGGTCAAAGGAAAATGGGAAATAGGCCTGAGAAAACCAGCCAATCGGCCCAGGGCCCAGGTGGGAAGTCAGAACACCTAACCCATCAGAACTGGAAGTGATCACAGCACCCATCTTGCCCCATCTTCCTGAGGGGGGGATGCCAGTGCCCAGAACCACACCCTGGCCTCCCGCCCAGGCTGGCACCCACTTTGTTTCACCTGCTGGTTTGAGTCCTCACTCGAGTTCTGCTCCTGGTGTGTCCAAGGCCTCCCACC... |
Task1_train_34701 | With a mutation on Chromosome 2, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GAGAAGCTCCCAGGAGGCTGAGAAGGCTGGGGTACCCTTATGACAACAAAGTATCTTTAGGACCCTAACACCCTATGTTCAAGGAGCCCTGGGCGTTCTCTAAGGGCTGCTTCATACACGGGCATCAGGCCTTCCCCACAGCCCTGCCAGGATGAGCAGTTATCCCAGCCCCAGGGTTCCACACAGGCCCCCAGACCTGAGGAGCAGGGCACCAGAGCAGCCCCCTTCCCAGGGAGGCGTCACTCTTCTGCCAGGACAGTGCTGTGCTGGACAACAGCTCACTCCAAGGCTCCCCTAGCATGAGCCAGACTGGAGGCAAT... | GAGAAGCTCCCAGGAGGCTGAGAAGGCTGGGGTACCCTTATGACAACAAAGTATCTTTAGGACCCTAACACCCTATGTTCAAGGAGCCCTGGGCGTTCTCTAAGGGCTGCTTCATACACGGGCATCAGGCCTTCCCCACAGCCCTGCCAGGATGAGCAGTTATCCCAGCCCCAGGGTTCCACACAGGCCCCCAGACCTGAGGAGCAGGGCACCAGAGCAGCCCCCTTCCCAGGGAGGCGTCACTCTTCTGCCAGGACAGTGCTGTGCTGGACAACAGCTCACTCCAAGGCTCCCCTAGCATGAGCCAGACTGGAGGCAAT... |
Task1_train_34702 | A mutation on Chromosome 2 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CTGAGCTCCCACCACCCTGTCAGCTGAGGGGCTGGCACAAGGTCCACCCAAATCCACAGTCTCTGGTCCACCCCTGTCTGGGCTCCACCTCCAGAATAAAGTCACCCAACAGGTTTTCCTGCCAAGTTCAGCCACCCTTGTGGAATGGGCATAGGCTTAGACCAGTGGGAAGGGAACCTCGCAGCTGTCTCTCCCAACATGGCCCCAGACATGCTGTCATTTCTTGCCTTTGTCTCCCCAAAAGCTCTTCTGAGTGTCCCACTTTCCTCTCTCCCAAAAGAGAAGCCCACTCTCTGATAGGAAAAGGAGCTTTGTCTCTC... | CTGAGCTCCCACCACCCTGTCAGCTGAGGGGCTGGCACAAGGTCCACCCAAATCCACAGTCTCTGGTCCACCCCTGTCTGGGCTCCACCTCCAGAATAAAGTCACCCAACAGGTTTTCCTGCCAAGTTCAGCCACCCTTGTGGAATGGGCATAGGCTTAGACCAGTGGGAAGGGAACCTCGCAGCTGTCTCTCCCAACATGGCCCCAGACATGCTGTCATTTCTTGCCTTTGTCTCCCCAAAAGCTCTTCTGAGTGTCCCACTTTCCTCTCTCCCAAAAGAGAAGCCCACTCTCTGATAGGAAAAGGAGCTTTGTCTCTC... |
Task1_train_34703 | A mutation located on Chromosome 2 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GTCCCAGCTCCATGTTGAATCTCCCTGTTCCCAACACCTCACTGTGACCCTGACTCTCACTCTCCCTCCTTGTAGATCTCTACCGATTCCTGGCATTCATCCTTCTCTGACCTCATCCCAAGCTGCCACCCCATCCCTGCCCCCATCCCAGCTTTGATTTCAACATCAATCACTGATCCCCATCTGAAGCTTGATCTAGGTCCTGTCTCTGAGCCTCACCCTATTCCCAACCTCAAGCCTTCCCTGATCCTTCCCCACACAGGCTAAACCCACACTCTCAGTTTTGCTTAAGCTAGTTTGACTTCTCTTTCTATCATTTG... | GTCCCAGCTCCATGTTGAATCTCCCTGTTCCCAACACCTCACTGTGACCCTGACTCTCACTCTCCCTCCTTGTAGATCTCTACCGATTCCTGGCATTCATCCTTCTCTGACCTCATCCCAAGCTGCCACCCCATCCCTGCCCCCATCCCAGCTTTGATTTCAACATCAATCACTGATCCCCATCTGAAGCTTGATCTAGGTCCTGTCTCTGAGCCTCACCCTATTCCCAACCTCAAGCCTTCCCTGATCCTTCCCCACACAGGCTAAACCCACACTCTCAGTTTTGCTTAAGCTAGTTTGACTTCTCTTTCTATCATTTG... |
Task1_train_34704 | A variant on Chromosome 2 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GATAAAAGTGTGTCGCACTTTCCGGTCATCCCACTCTCCAGGCCCGAAGCTATCACTCACTGCTCTCTCCTCCCCATCATAGCCATGGCCTGGGCCTAGGGACAGATGACACTTGACTCAGCTGGGGACCTGAGACATGTGGCGTCAATCCCAAAGCCTCCCTGACAATCTCAAAGTCTCAGGGATCTCCAGCCAAAAGACAAGTGTTATAACAGGAACTCTTCTCCCAAGCTGGGGTCTTCTAGACACCCTCAGAGTGACCCAGAGCCGGCCTGTCACGAGGGGGCTTAGGTGGGAAACGTTCCTCACGTGCATCTGTG... | GATAAAAGTGTGTCGCACTTTCCGGTCATCCCACTCTCCAGGCCCGAAGCTATCACTCACTGCTCTCTCCTCCCCATCATAGCCATGGCCTGGGCCTAGGGACAGATGACACTTGACTCAGCTGGGGACCTGAGACATGTGGCGTCAATCCCAAAGCCTCCCTGACAATCTCAAAGTCTCAGGGATCTCCAGCCAAAAGACAAGTGTTATAACAGGAACTCTTCTCCCAAGCTGGGGTCTTCTAGACACCCTCAGAGTGACCCAGAGCCGGCCTGTCACGAGGGGGCTTAGGTGGGAAACGTTCCTCACGTGCATCTGTG... |
Task1_train_34705 | A variant was discovered on Chromosome 2. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GCTGCGGATGGGTAACAGGGCGTGGGCTGGCACACTTACTTGCACCAGTGCCCAGAGAGGGGGTGCAGGCTGAGGAGCTGCCCAGAGCACCGCTCACACTCCCAGAGTACCTGAAGTCGGCATTTCAATGACAGGTGAGTAGTGGCCCCTAGGGACAGAGCCTGATTGGGGGGTGGAGTGGAGGAGATCACTAGGCTGGTGGAGACTTGAGGAAGCAAGAAAGCCCTTGGTCCCCTGTGGAAGCCTCTGGTCCCCCGTGGGAGTCCTAGTCTAGAACACAGTTCTGGACACCAGACTCAATCTCACTGGGTGGAGTCCTT... | GCTGCGGATGGGTAACAGGGCGTGGGCTGGCACACTTACTTGCACCAGTGCCCAGAGAGGGGGTGCAGGCTGAGGAGCTGCCCAGAGCACCGCTCACACTCCCAGAGTACCTGAAGTCGGCATTTCAATGACAGGTGAGTAGTGGCCCCTAGGGACAGAGCCTGATTGGGGGGTGGAGTGGAGGAGATCACTAGGCTGGTGGAGACTTGAGGAAGCAAGAAAGCCCTTGGTCCCCTGTGGAAGCCTCTGGTCCCCCGTGGGAGTCCTAGTCTAGAACACAGTTCTGGACACCAGACTCAATCTCACTGGGTGGAGTCCTT... |
Task1_train_34706 | A genomic change on Chromosome 2 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | ACCGTGCACCCAGTACCTATCTTCTTAACTCCCTGAAAGAGGGGCTGGAAGGCCTCCATGGTGAATCTTGCTCTTCTTTTCTCCTGGGGCCCTCAGTGGCCATGAATATGCAGACTGCAGGGCTTGAAATGGACATCTGTGATGGGCATTTCCGCCAGAATGGCGGCTGTGGCTATGTGCTGAAGCCAGACTTCCTGCGTGATATCCAGAGTTCTTTCCACCCTGAGAAGCCCATCAGCCCTTTCAAAGCCCAGACTCTCTTAATCCAGGTACAGTGGAAATAAACTGTTGGGAAGAAACTGAGATAACTGGGATAGAAG... | ACCGTGCACCCAGTACCTATCTTCTTAACTCCCTGAAAGAGGGGCTGGAAGGCCTCCATGGTGAATCTTGCTCTTCTTTTCTCCTGGGGCCCTCAGTGGCCATGAATATGCAGACTGCAGGGCTTGAAATGGACATCTGTGATGGGCATTTCCGCCAGAATGGCGGCTGTGGCTATGTGCTGAAGCCAGACTTCCTGCGTGATATCCAGAGTTCTTTCCACCCTGAGAAGCCCATCAGCCCTTTCAAAGCCCAGACTCTCTTAATCCAGGTACAGTGGAAATAAACTGTTGGGAAGAAACTGAGATAACTGGGATAGAAG... |
Task1_train_34707 | This mutation occurs on Chromosome 2. Does this change lead to a known medical condition, or is it benign? | Benign | CCCCACCCTGCTGTCTACTCCCAATGTGAAATTGATGTTGGCCCTGAATTGGAACAAGGACCAACCTTGGTAAGGTTAGGTTTGCCAGGGAACAAAGGAACCCTTCAGGCCTGTCGAAACCACACAGACTCACCTGTATGCTTGGTCATGTGGTATTTCAGCTGGTTGACCCACTTGCACTTGTAGCCACACTCAGGGCACAGGTACTTCCGTTCCTCCTTGTGGATCCGCATGTGGTACTGGAAGAGGCAAGAGCAAAAAGCAGAAAATATAGTAAGTGCTCAATAAATGTTAGCTGTTATTATCCAGGTTATTCTTGC... | CCCCACCCTGCTGTCTACTCCCAATGTGAAATTGATGTTGGCCCTGAATTGGAACAAGGACCAACCTTGGTAAGGTTAGGTTTGCCAGGGAACAAAGGAACCCTTCAGGCCTGTCGAAACCACACAGACTCACCTGTATGCTTGGTCATGTGGTATTTCAGCTGGTTGACCCACTTGCACTTGTAGCCACACTCAGGGCACAGGTACTTCCGTTCCTCCTTGTGGATCCGCATGTGGTACTGGAAGAGGCAAGAGCAAAAAGCAGAAAATATAGTAAGTGCTCAATAAATGTTAGCTGTTATTATCCAGGTTATTCTTGC... |
Task1_train_34708 | This variant is present on Chromosome 2. Is the change likely to result in a pathogenic outcome? | Benign | ATGATCATAGCTCACTGCAGCCTCAAATTCCTAGGCTCAAGCAATCCTCCCACCTCAGCCTCCTGAGTAGCTGGGACTACAGGTACTTGCCACCATGCCCAGCTGATTAAGAAAAAGTTTTTGTAATGGGATCTCGCTCTGCTGCCGAGTGGTCTTCAACTCTTGGCTTCAAGCAATCCTCCTAACTTGGTATCTCAAAGTGTTAAGATTACAGGCGTGAGCCACATTATGGAACTTTATCTTTACAACAACCCTATGAAGTTGGTATTATCTCATTTTTAACAGATGAAGAATCTGAGGCTTGGTAAAGGAACTTTCCC... | ATGATCATAGCTCACTGCAGCCTCAAATTCCTAGGCTCAAGCAATCCTCCCACCTCAGCCTCCTGAGTAGCTGGGACTACAGGTACTTGCCACCATGCCCAGCTGATTAAGAAAAAGTTTTTGTAATGGGATCTCGCTCTGCTGCCGAGTGGTCTTCAACTCTTGGCTTCAAGCAATCCTCCTAACTTGGTATCTCAAAGTGTTAAGATTACAGGCGTGAGCCACATTATGGAACTTTATCTTTACAACAACCCTATGAAGTTGGTATTATCTCATTTTTAACAGATGAAGAATCTGAGGCTTGGTAAAGGAACTTTCCC... |
Task1_train_34709 | Chromosome 2 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GCATGTGAAGTCACAAAAGGGGCAGTGTAGCGGGGGCTGGCCAGCATCCCCATCCCCATCTGAGGCTGCCACGGCTGCTGAAGTCTCCTCATGCTGTTCCAGGTAGTGCTTTACCAGGCCCACCCGCTCCCGGGCAGCAAAGTCACAGAGCTGACAGCGGTGGCTGAAATGCTGCTGCCTCCGGTGCTCATCCAGAGCCAGTCGGCTAGGGAAGGCCTCCTGGCAGGCCCCACACTCAAGCCGTGGGTGCTGTTTACGGGTGTGTCCTCGTAAGCTGGCAGGGCTGGGGCACAGCAACCCACAGCGGGAACAGTGCAGGG... | GCATGTGAAGTCACAAAAGGGGCAGTGTAGCGGGGGCTGGCCAGCATCCCCATCCCCATCTGAGGCTGCCACGGCTGCTGAAGTCTCCTCATGCTGTTCCAGGTAGTGCTTTACCAGGCCCACCCGCTCCCGGGCAGCAAAGTCACAGAGCTGACAGCGGTGGCTGAAATGCTGCTGCCTCCGGTGCTCATCCAGAGCCAGTCGGCTAGGGAAGGCCTCCTGGCAGGCCCCACACTCAAGCCGTGGGTGCTGTTTACGGGTGTGTCCTCGTAAGCTGGCAGGGCTGGGGCACAGCAACCCACAGCGGGAACAGTGCAGGG... |
Task1_train_34710 | An alteration has been detected on Chromosome 2. Is it pathogenic, and if so, what disease is involved? | Benign | ATGTCCACATTCTAGATGTTATCTACATAGCTTTCAGTCCAAAGCTATCAGAATGGTGAGAGCTGGTGGAGCTGGTTCAGTGATTAGGGGCAGATGATAGAGGTGGTGCCTACTCATTGTGACTAAGTCAGTAGTCTGGAGGAGGGAAGAGTAGAAGAGGAGTTGGACTTCTTTTCTATTTCTTTTTTCTTTGAGATGGAGTCTTACTCTGTCACCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAAGCTCCGCCCTCCAGATTCACACCATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGTG... | ATGTCCACATTCTAGATGTTATCTACATAGCTTTCAGTCCAAAGCTATCAGAATGGTGAGAGCTGGTGGAGCTGGTTCAGTGATTAGGGGCAGATGATAGAGGTGGTGCCTACTCATTGTGACTAAGTCAGTAGTCTGGAGGAGGGAAGAGTAGAAGAGGAGTTGGACTTCTTTTCTATTTCTTTTTTCTTTGAGATGGAGTCTTACTCTGTCACCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAAGCTCCGCCCTCCAGATTCACACCATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGTG... |
Task1_train_34711 | Chromosome 2 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | AAAGAAAAAAAATATGCGAATAACCTAGAGAAAATGGCAAAGAAGGGGCTTGGAGGGTGTATGTGTGTGTGTGGCAAGGGAGAAGGGAGGAACATTCTGATGTGTCCCTTTGCAGAGATTCTCCTACCTGCCCAGGACTGACCCATTCACCACATCCAGGCTTTTAGTAGAGAGATAAGAAATCATGGGCTCATTTTCCACCCCCAGCCTGCAGGTGTTTCAGGAGGCTGCCAACCTTTTTCTGGACCTGTTGGGGAAACTGCTGGCCCAACCAGATGACTCTGAGCAGACTTTGCGGAGGGACAGCCTTATGGTAATCT... | AAAGAAAAAAAATATGCGAATAACCTAGAGAAAATGGCAAAGAAGGGGCTTGGAGGGTGTATGTGTGTGTGTGGCAAGGGAGAAGGGAGGAACATTCTGATGTGTCCCTTTGCAGAGATTCTCCTACCTGCCCAGGACTGACCCATTCACCACATCCAGGCTTTTAGTAGAGAGATAAGAAATCATGGGCTCATTTTCCACCCCCAGCCTGCAGGTGTTTCAGGAGGCTGCCAACCTTTTTCTGGACCTGTTGGGGAAACTGCTGGCCCAACCAGATGACTCTGAGCAGACTTTGCGGAGGGACAGCCTTATGGTAATCT... |
Task1_train_34712 | This sequence variant lies on Chromosome 2. Is it clinically significant, and what condition might it cause if any? | Benign | ACCAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAACCTCCACCTCCTGGGTTCAAGCGATTCTCCTGCCTTATCCTCCTGAGTAGCTGGGACAACAGGTGCACACCTCCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACAATGTTGGCCAGGCTGGTCTGGAACTCCTGACTTCCTGATCCCCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCTACCTCAGTGGCTGAATTCTTTATAATTTATAAAACATTTTCACATGTTATCCCACAACACACTTGAAATATAGAC... | ACCAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAACCTCCACCTCCTGGGTTCAAGCGATTCTCCTGCCTTATCCTCCTGAGTAGCTGGGACAACAGGTGCACACCTCCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACAATGTTGGCCAGGCTGGTCTGGAACTCCTGACTTCCTGATCCCCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCTACCTCAGTGGCTGAATTCTTTATAATTTATAAAACATTTTCACATGTTATCCCACAACACACTTGAAATATAGAC... |
Task1_train_34713 | This alteration occurs on Chromosome 2. Is it associated with a disease or is it a benign variant? | Benign | CAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAACCTCCACCTCCTGGGTTCAAGCGATTCTCCTGCCTTATCCTCCTGAGTAGCTGGGACAACAGGTGCACACCTCCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACAATGTTGGCCAGGCTGGTCTGGAACTCCTGACTTCCTGATCCCCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCTACCTCAGTGGCTGAATTCTTTATAATTTATAAAACATTTTCACATGTTATCCCACAACACACTTGAAATATAGACAC... | CAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAACCTCCACCTCCTGGGTTCAAGCGATTCTCCTGCCTTATCCTCCTGAGTAGCTGGGACAACAGGTGCACACCTCCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACAATGTTGGCCAGGCTGGTCTGGAACTCCTGACTTCCTGATCCCCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCTACCTCAGTGGCTGAATTCTTTATAATTTATAAAACATTTTCACATGTTATCCCACAACACACTTGAAATATAGACAC... |
Task1_train_34714 | This alteration on Chromosome 2 may affect genome function. Does it lead to a disease or is it benign? | Benign | TCAGCAGACATACACATGAGTTGTGAGGTCAGAGGGTTAAGGTTTGATAAGAAAATGAAATAAGACGACAGGGAAATACTAGGTGGGAAAGCGGAAGGAATTATTTCTGGGACTTCCTTTACTTGTAAGTCAGGGACAGGAATGAATAAAAGCATTTGGATTCCTGACTTCTGTCTTTCCCCCCGCCCTCTTTCACTTTTATCTCTAGCAGGGGAAGGCTAGCCTAATCAGGGATATGTCCAGTTCAGAAATGTGGACCGTTTTGTGGCACCGCTTCTCCATGGTCCTGAGGCTCCCCGAGGAGGCATCTGCACAGGAAG... | TCAGCAGACATACACATGAGTTGTGAGGTCAGAGGGTTAAGGTTTGATAAGAAAATGAAATAAGACGACAGGGAAATACTAGGTGGGAAAGCGGAAGGAATTATTTCTGGGACTTCCTTTACTTGTAAGTCAGGGACAGGAATGAATAAAAGCATTTGGATTCCTGACTTCTGTCTTTCCCCCCGCCCTCTTTCACTTTTATCTCTAGCAGGGGAAGGCTAGCCTAATCAGGGATATGTCCAGTTCAGAAATGTGGACCGTTTTGTGGCACCGCTTCTCCATGGTCCTGAGGCTCCCCGAGGAGGCATCTGCACAGGAAG... |
Task1_train_34715 | Chromosome 2 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CAGACTGGACACTGATTTCTCCCCAGGGTATCTTTCTATCAGTATCCTTTTTGGGAGTGCATTGATCTCTCTTCAAGAGGAGGCAGCCCAGAACTGGGTTAACCCACAGAGGTTTATTTTTTTTGCTTTTGCCTGGGGACAGGAAGCAGTGTCTGCACTAGAGCTGCTCTAAGATGGGGAAGGGACTGAATAGGTGTAGCCCTGGGAGCTGTGGGGAAGCAGGGGTATCTGGGCGTCTTGCCTGTTCCATTGGGTCTCCATTTTTGGTGTTACCAGGCATGGCAGCCCTGCTGAGCCTGGCCATGGCCACCTTTACCCAG... | CAGACTGGACACTGATTTCTCCCCAGGGTATCTTTCTATCAGTATCCTTTTTGGGAGTGCATTGATCTCTCTTCAAGAGGAGGCAGCCCAGAACTGGGTTAACCCACAGAGGTTTATTTTTTTTGCTTTTGCCTGGGGACAGGAAGCAGTGTCTGCACTAGAGCTGCTCTAAGATGGGGAAGGGACTGAATAGGTGTAGCCCTGGGAGCTGTGGGGAAGCAGGGGTATCTGGGCGTCTTGCCTGTTCCATTGGGTCTCCATTTTTGGTGTTACCAGGCATGGCAGCCCTGCTGAGCCTGGCCATGGCCACCTTTACCCAG... |
Task1_train_34716 | A genomic change on Chromosome 2 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GATGGCGCGATCTCGGCTCACTGCAACCTCCGCCTCCCGAGGTCAAGCGATTCTCCTGCCTCAGGCTCCCAAGTAGCTGGGATTACAGGCACCCTCCTCCGTGCATGGCTAATTTTTGTATTTTTAGTAGAGAGCGTTTCACCATGCTGGCCAGGCTGGTCTTGAACTCCTGACCTCGTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGATGTAGCCACCGTGCCCAGCCTTTTTTTTTTTTTTTTTTTTTTTGTGAGACAGGGTCTCACTCTGTCACCCAGGCTGGAGAGCAGTGGTGCTATCTTGGTT... | GATGGCGCGATCTCGGCTCACTGCAACCTCCGCCTCCCGAGGTCAAGCGATTCTCCTGCCTCAGGCTCCCAAGTAGCTGGGATTACAGGCACCCTCCTCCGTGCATGGCTAATTTTTGTATTTTTAGTAGAGAGCGTTTCACCATGCTGGCCAGGCTGGTCTTGAACTCCTGACCTCGTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGATGTAGCCACCGTGCCCAGCCTTTTTTTTTTTTTTTTTTTTTTTGTGAGACAGGGTCTCACTCTGTCACCCAGGCTGGAGAGCAGTGGTGCTATCTTGGTT... |
Task1_train_34717 | A variant on Chromosome 2 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TTCTTCCATGGGGCCTTCTCCTGGACCCTCCTCTACACCAGCTGGCCTGTCTTCCTCATGTCACAGTACACGCTAGACATGATCGTTGCTGGGGACATGTACATAGATAAGGCTGTGGCCTGAGACCATGAGCCCCTCACCTGGCACACCAGGGAGTGAGAAATTCTAAGTTCATGTTTCCATTTGGAGGGTATGTGTGTACAGACACAGTCTAGTTTTTGATAGACTAAGTACCGGAGGCATAGTTATTTACATAACACTTGCATATTTACATACTTTTTTTGTAGATAAATTTTATATTGACTCATTTTGTGCCCCGT... | TTCTTCCATGGGGCCTTCTCCTGGACCCTCCTCTACACCAGCTGGCCTGTCTTCCTCATGTCACAGTACACGCTAGACATGATCGTTGCTGGGGACATGTACATAGATAAGGCTGTGGCCTGAGACCATGAGCCCCTCACCTGGCACACCAGGGAGTGAGAAATTCTAAGTTCATGTTTCCATTTGGAGGGTATGTGTGTACAGACACAGTCTAGTTTTTGATAGACTAAGTACCGGAGGCATAGTTATTTACATAACACTTGCATATTTACATACTTTTTTTGTAGATAAATTTTATATTGACTCATTTTGTGCCCCGT... |
Task1_train_34718 | Chromosome 2 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GGTCTCTAATTACCCTCTGCTCCCAGATGCTCTACTCATTCATTTGAGATGGGAATCCCAGCTAAGTGTTCAAATAGGAGCATTCTGATGAGAGCAGTTCCCCCAGGTATGAATCCCTAAGGAATTAACCTTCAGGGGTCTGGTATACCAAAACCAAATGTCAGCTCTCTCCTTGGGCAGAACGAAGGCCAGGAGTTGAGGGATTTCTGGAAGTGCGTGAGACTTCCCGTGAAGTCTTCCCCTACCAAGCCAAATATTGCCTGCACCCAGCAGTGATGTCACCCTAATGCGCAGGGCTTGGTTCACTGCCATTCTGCTCA... | GGTCTCTAATTACCCTCTGCTCCCAGATGCTCTACTCATTCATTTGAGATGGGAATCCCAGCTAAGTGTTCAAATAGGAGCATTCTGATGAGAGCAGTTCCCCCAGGTATGAATCCCTAAGGAATTAACCTTCAGGGGTCTGGTATACCAAAACCAAATGTCAGCTCTCTCCTTGGGCAGAACGAAGGCCAGGAGTTGAGGGATTTCTGGAAGTGCGTGAGACTTCCCGTGAAGTCTTCCCCTACCAAGCCAAATATTGCCTGCACCCAGCAGTGATGTCACCCTAATGCGCAGGGCTTGGTTCACTGCCATTCTGCTCA... |
Task1_train_34719 | Chromosome 2 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CCAGGAGCCCAGGAACCGGGACAGGAGGCTGGGGAGGGCCTAGCCCCTGCGGGAGGCCAGACCAACCGTTCACTGAGCAAATGGGAAAACCAAGAGGCCGGGAAATGACTTGCCCAAGGCCATAGAAGTCGCGGGGACAGAGGCGGACTAGAATCCGGGTTTCCACCTCCAGAAGGGTTTCTGTTCTGGGCCACGGCCCCCTTCGCCACCCGCTGGAGCCGGCTCAGCCCGTATTACGACGCAGAATGGAGCCTGGCAGCCCAGAAGCTGCGGGCAGGGCAAGGCAGGGCGGGTGGGGCCGGATGGGAGCCGGATCTCCC... | CCAGGAGCCCAGGAACCGGGACAGGAGGCTGGGGAGGGCCTAGCCCCTGCGGGAGGCCAGACCAACCGTTCACTGAGCAAATGGGAAAACCAAGAGGCCGGGAAATGACTTGCCCAAGGCCATAGAAGTCGCGGGGACAGAGGCGGACTAGAATCCGGGTTTCCACCTCCAGAAGGGTTTCTGTTCTGGGCCACGGCCCCCTTCGCCACCCGCTGGAGCCGGCTCAGCCCGTATTACGACGCAGAATGGAGCCTGGCAGCCCAGAAGCTGCGGGCAGGGCAAGGCAGGGCGGGTGGGGCCGGATGGGAGCCGGATCTCCC... |
Task1_train_34720 | Here’s a variant located on Chromosome 2. What is the predicted biological effect — harmless or disease-causing? | Benign | TTATAAAAGAGGCCTGTGGAAGCTTGTTTGCTCCCTCCACCATGTGAGGACACAGCAAGAAGCCACTGAACCAGGAAGTGGGCCCCCACCAAACCTGCCCATGTCTTGATCTTGGGCTCCCCAGCCTTTTTAATTAAGATAAATTATAATAAATTAAATTACAATAAATTATAATAAATTTGTGGTCTTTATAAGCCACCCAATCTATGGTAACTTGTTTTAGCAGCCAGAATGGACTAAGACACTTGGTGTCCACCTTCTACCTGACAAGCCCTCTTGGTTGTCTCATTAGCATCTCAAACTTGGCCAGAACCAAACTC... | TTATAAAAGAGGCCTGTGGAAGCTTGTTTGCTCCCTCCACCATGTGAGGACACAGCAAGAAGCCACTGAACCAGGAAGTGGGCCCCCACCAAACCTGCCCATGTCTTGATCTTGGGCTCCCCAGCCTTTTTAATTAAGATAAATTATAATAAATTAAATTACAATAAATTATAATAAATTTGTGGTCTTTATAAGCCACCCAATCTATGGTAACTTGTTTTAGCAGCCAGAATGGACTAAGACACTTGGTGTCCACCTTCTACCTGACAAGCCCTCTTGGTTGTCTCATTAGCATCTCAAACTTGGCCAGAACCAAACTC... |
Task1_train_34721 | This variant lies on Chromosome 2. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CCTCCTGCCAGAGCCCTCCCACTCACAGAGAGGCTGCTGGTGAGCCCAACGCCCACCAGCCGGAGCATGTAGTGGGTGGTGGCAGCGGGGTTGGCATTTGGGGACAGGCCGGCTTCCCAGACCCACATCCCCACTTGGAACAGGTACTTGGTCTCCTCCAAAGGGCTGAAGGTCCACGTCAGCGTCTGGGGTCACAGAAATGATCCCTGCAGTGGCCTTCGGAAGCCCCTCCACAGGTACCTGGCCATCCGAGGCCCCATGGCAGGGCGTCATGCTACGTTAGCCCTTTCTCAGAATCTACCCTATGCCAGGCATTGTAC... | CCTCCTGCCAGAGCCCTCCCACTCACAGAGAGGCTGCTGGTGAGCCCAACGCCCACCAGCCGGAGCATGTAGTGGGTGGTGGCAGCGGGGTTGGCATTTGGGGACAGGCCGGCTTCCCAGACCCACATCCCCACTTGGAACAGGTACTTGGTCTCCTCCAAAGGGCTGAAGGTCCACGTCAGCGTCTGGGGTCACAGAAATGATCCCTGCAGTGGCCTTCGGAAGCCCCTCCACAGGTACCTGGCCATCCGAGGCCCCATGGCAGGGCGTCATGCTACGTTAGCCCTTTCTCAGAATCTACCCTATGCCAGGCATTGTAC... |
Task1_train_34722 | This is a variant located on Chromosome 2. Is this mutation a likely cause of disease or not? | Benign | AAACTGGATTGGAAGCCGGCGGTCTGGCCCCAGGCTCTGTGCTTTTCAGCCCTATGTCCTCTTGCTTGTCAGGTCAGGCAGGGCTTCTAAGGGCCTTGGGGTGGCCTGGGAATTATGATCTCCTGAGGATGGGGCTGGCTCTGCCTCTCATAGGGCAGGGTGCTTCCCAAAGGCAGGGGCTGCTGGTGCGGCTGTCATATCCCTGGGCCCGAGCCCAGGACTTGGGGCACCCAGGCATTCAGTAAACAGGACACAAACAAATGCAGGAGCTGGAGGGTTTTGAACCTGAGAGTCATAGGAGCCAGTGAGTATTTCCAATG... | AAACTGGATTGGAAGCCGGCGGTCTGGCCCCAGGCTCTGTGCTTTTCAGCCCTATGTCCTCTTGCTTGTCAGGTCAGGCAGGGCTTCTAAGGGCCTTGGGGTGGCCTGGGAATTATGATCTCCTGAGGATGGGGCTGGCTCTGCCTCTCATAGGGCAGGGTGCTTCCCAAAGGCAGGGGCTGCTGGTGCGGCTGTCATATCCCTGGGCCCGAGCCCAGGACTTGGGGCACCCAGGCATTCAGTAAACAGGACACAAACAAATGCAGGAGCTGGAGGGTTTTGAACCTGAGAGTCATAGGAGCCAGTGAGTATTTCCAATG... |
Task1_train_34723 | This alteration occurs on Chromosome 2. Is it associated with a disease or is it a benign variant? | Benign | CTGTCTATACCAAAATTTTTTTTAAAAAATTAGCCAGGCATGGTGGTGCATGCCTACAGTCCCAGCTACCTGAGAGGCTGAGGAAGGAGGATTGCTTGAGCCTAGGAGGTCATGGCTACAGTTAGCCATGTTAATGCCACTATACTCCAGCCTGGGCAAGGGAGTGAGACCCTGTCTCAAAAAAACAAGAAAGAAAGAAAAGAAAGAAAAGAAAGAGAAAGAAAGAGAGAGAGGAAGAAAAGAAAGAAAAAAAAGAAAGAAGAAATTAGATAAACTTTAATGTGTGTTTATGAGAAAGACTCTCAGCAAAGCAGGAATAG... | CTGTCTATACCAAAATTTTTTTTAAAAAATTAGCCAGGCATGGTGGTGCATGCCTACAGTCCCAGCTACCTGAGAGGCTGAGGAAGGAGGATTGCTTGAGCCTAGGAGGTCATGGCTACAGTTAGCCATGTTAATGCCACTATACTCCAGCCTGGGCAAGGGAGTGAGACCCTGTCTCAAAAAAACAAGAAAGAAAGAAAAGAAAGAAAAGAAAGAGAAAGAAAGAGAGAGAGGAAGAAAAGAAAGAAAAAAAAGAAAGAAGAAATTAGATAAACTTTAATGTGTGTTTATGAGAAAGACTCTCAGCAAAGCAGGAATAG... |
Task1_train_34724 | A change on Chromosome 2 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | AGGCTGCAGTATAATGGCACAATCTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGTGATTTTCTCGCCTTAGCTTCCCGAGTAGCTGGGATTACAGGCACCCGCCATCATGCCTGGCTGATTTTTGTATTTCTGTAGAGATGGGGTTTCACCATGTTGGTCAGGCAGGTCTTGAACTCCTGACCTCAGGTGATCCACCCACCTTGGCCTCCCAAAGAGCTGGGATTACAGGTGTGAGCCATCATGCCCGGCCAGCATTTTATTTTATCTTTGACCAAGTATTGCTTTTATATTGTTGCATAATATAAGGATATAGT... | AGGCTGCAGTATAATGGCACAATCTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGTGATTTTCTCGCCTTAGCTTCCCGAGTAGCTGGGATTACAGGCACCCGCCATCATGCCTGGCTGATTTTTGTATTTCTGTAGAGATGGGGTTTCACCATGTTGGTCAGGCAGGTCTTGAACTCCTGACCTCAGGTGATCCACCCACCTTGGCCTCCCAAAGAGCTGGGATTACAGGTGTGAGCCATCATGCCCGGCCAGCATTTTATTTTATCTTTGACCAAGTATTGCTTTTATATTGTTGCATAATATAAGGATATAGT... |
Task1_train_34725 | A mutation on Chromosome 2 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GGTGTGGTTCCTGCTGTTCCTGGACCTCACGACGGAGCTTGGAGCCTGGGTGAGCATCATGTCCTTGGGACACAGTCCAAAGGGAGCACTCTGAGTATGGAGCTGGGAAGAGAGCAGAGGGGAGAGGAGACAGGAGTGACATGAGAAAGAGAGGCTGAGGGAGGAGACTCTCATGGCCATCCTTGTCATGGAGGAGAGGGTCTGCTTCCCAGCTCTGGCAACAGGTGCTACCTGGCACCATGAGGAATGAGGCTGTACACGAGATCCAGGGCTTTGCCTGGGAGCCCAGGGACTCACCCTCAGGGAAGGCACTCCAAAGA... | GGTGTGGTTCCTGCTGTTCCTGGACCTCACGACGGAGCTTGGAGCCTGGGTGAGCATCATGTCCTTGGGACACAGTCCAAAGGGAGCACTCTGAGTATGGAGCTGGGAAGAGAGCAGAGGGGAGAGGAGACAGGAGTGACATGAGAAAGAGAGGCTGAGGGAGGAGACTCTCATGGCCATCCTTGTCATGGAGGAGAGGGTCTGCTTCCCAGCTCTGGCAACAGGTGCTACCTGGCACCATGAGGAATGAGGCTGTACACGAGATCCAGGGCTTTGCCTGGGAGCCCAGGGACTCACCCTCAGGGAAGGCACTCCAAAGA... |
Task1_train_34726 | This mutation occurs on Chromosome 2. Does this change lead to a known medical condition, or is it benign? | Benign | CACTCCAGCCTGGGTGACAGAGTGAGACTGTGTCAAAAAAAAAAAGAAAAAAGAAAAAAAGAAACTTGTGGACAATATATCCTACATCACATGTGACAACCACAACTACCTGAAACATGCTCACTGTAAAGAATAAAATTTATAATAACATGTATTTCATTACGTGAAGGCTTAAGCACAACTAAACCAGAAGACAATAAAGTACAATGAAGTAGTCCAATCCCACACCCTATGAGAATTGCTGTGGTTGCAATAGCTGCAATGCCAGCTGATATTGGTGCTTTATCGGTGACTCTGATGTTGGTAACCCGATTTTCAAA... | CACTCCAGCCTGGGTGACAGAGTGAGACTGTGTCAAAAAAAAAAAGAAAAAAGAAAAAAAGAAACTTGTGGACAATATATCCTACATCACATGTGACAACCACAACTACCTGAAACATGCTCACTGTAAAGAATAAAATTTATAATAACATGTATTTCATTACGTGAAGGCTTAAGCACAACTAAACCAGAAGACAATAAAGTACAATGAAGTAGTCCAATCCCACACCCTATGAGAATTGCTGTGGTTGCAATAGCTGCAATGCCAGCTGATATTGGTGCTTTATCGGTGACTCTGATGTTGGTAACCCGATTTTCAAA... |
Task1_train_34727 | A variant affecting Chromosome 2 has been observed. Determine if it's benign or associated with disease. | Benign | CCACACCCTATGAGAATTGCTGTGGTTGCAATAGCTGCAATGCCAGCTGATATTGGTGCTTTATCGGTGACTCTGATGTTGGTAACCCGATTTTCAAAATGGCAAACAAACTCTTGGTTAAGGTGCCAAGCAAAATAAAGTCGTCTTAATTTACATGGGAATGAATTCCTAGCAAACTGAGTCTTTTCAAAACGCACAAACGCTATTTCACGTTTACATGTGCAAAGACAGTTCTAGGCTCAGATAAACAGGGTTTTCATATACATAAAGCTGGTCATTCAAAAGTTGTCTTGGGAATTCTTCACAGTACGGGAGGTCTG... | CCACACCCTATGAGAATTGCTGTGGTTGCAATAGCTGCAATGCCAGCTGATATTGGTGCTTTATCGGTGACTCTGATGTTGGTAACCCGATTTTCAAAATGGCAAACAAACTCTTGGTTAAGGTGCCAAGCAAAATAAAGTCGTCTTAATTTACATGGGAATGAATTCCTAGCAAACTGAGTCTTTTCAAAACGCACAAACGCTATTTCACGTTTACATGTGCAAAGACAGTTCTAGGCTCAGATAAACAGGGTTTTCATATACATAAAGCTGGTCATTCAAAAGTTGTCTTGGGAATTCTTCACAGTACGGGAGGTCTG... |
Task1_train_34728 | Assess the clinical impact of this variant found on Chromosome 2. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TTTTCAAAATGGCAAACAAACTCTTGGTTAAGGTGCCAAGCAAAATAAAGTCGTCTTAATTTACATGGGAATGAATTCCTAGCAAACTGAGTCTTTTCAAAACGCACAAACGCTATTTCACGTTTACATGTGCAAAGACAGTTCTAGGCTCAGATAAACAGGGTTTTCATATACATAAAGCTGGTCATTCAAAAGTTGTCTTGGGAATTCTTCACAGTACGGGAGGTCTGAGCATTTCATGATGTCTAGCATCCCGCCCAGGTTGACGAAATGCCAGTAGCACCCCATCCCCTTGAATCCTTTTGACAATGAAAAAATAG... | TTTTCAAAATGGCAAACAAACTCTTGGTTAAGGTGCCAAGCAAAATAAAGTCGTCTTAATTTACATGGGAATGAATTCCTAGCAAACTGAGTCTTTTCAAAACGCACAAACGCTATTTCACGTTTACATGTGCAAAGACAGTTCTAGGCTCAGATAAACAGGGTTTTCATATACATAAAGCTGGTCATTCAAAAGTTGTCTTGGGAATTCTTCACAGTACGGGAGGTCTGAGCATTTCATGATGTCTAGCATCCCGCCCAGGTTGACGAAATGCCAGTAGCACCCCATCCCCTTGAATCCTTTTGACAATGAAAAAATAG... |
Task1_train_34729 | Here is a genetic alteration on Chromosome 2. Based on the data, is it a benign variant or a cause of disease? | Benign | GGTCGAGAGCACCATTCCCCTTTCTGGGTTATCACTTGGCCTGGGGGCATGACCCATCCCCAGTTTTTGCAGGCTGACATCCGCTTGAATTGCCCATTTTTTTCTATCTCTGAGTCGTGAGTCGCGAGTTAGGCCTGGAGGTGCCATTACCCCATCAGTAGGCGCCTTTCCACCTTCTGAGATGGATGCATGAGCCTGTCTCACCCACTCACTGCTGAGGTGCCTGTCTCTCCCTAAGGTTGCTGTCTTCCTCGTCCCTCCGGCCCTTCTTCCTACTCAGCGTCTCACTTTTGGCCTATTTTCTGCTGGATCTCTGGCAG... | GGTCGAGAGCACCATTCCCCTTTCTGGGTTATCACTTGGCCTGGGGGCATGACCCATCCCCAGTTTTTGCAGGCTGACATCCGCTTGAATTGCCCATTTTTTTCTATCTCTGAGTCGTGAGTCGCGAGTTAGGCCTGGAGGTGCCATTACCCCATCAGTAGGCGCCTTTCCACCTTCTGAGATGGATGCATGAGCCTGTCTCACCCACTCACTGCTGAGGTGCCTGTCTCTCCCTAAGGTTGCTGTCTTCCTCGTCCCTCCGGCCCTTCTTCCTACTCAGCGTCTCACTTTTGGCCTATTTTCTGCTGGATCTCTGGCAG... |
Task1_train_34730 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GGTATCTGAGGCCTCCAGGGGTCATGTCATGTCTCCCCAGTGAGGGTGCGGGGTCAGGCGCCCGGCCGCACCTGCTGAGTGTGCCCGAGTTGTGCAGATACCTGGCTGAGAGCTGGCTCACCTTCCAGATTCACCTGCAGGAGCTGCTGCAGTACAAGAGGCAGAATCCAGCTCAGGTAACCTCCCCTACATCATACAACAGTTCACTACACTGAAGGGGAATAGAGGTGGCGGGGGATGGGAGTGGAGTGATATAAACTCCCCGCTTGGAGACCCTGAAAGAAGAGGCCTGGGCGCCTTCTTGAGGCAACATTCACAGC... | GGTATCTGAGGCCTCCAGGGGTCATGTCATGTCTCCCCAGTGAGGGTGCGGGGTCAGGCGCCCGGCCGCACCTGCTGAGTGTGCCCGAGTTGTGCAGATACCTGGCTGAGAGCTGGCTCACCTTCCAGATTCACCTGCAGGAGCTGCTGCAGTACAAGAGGCAGAATCCAGCTCAGGTAACCTCCCCTACATCATACAACAGTTCACTACACTGAAGGGGAATAGAGGTGGCGGGGGATGGGAGTGGAGTGATATAAACTCCCCGCTTGGAGACCCTGAAAGAAGAGGCCTGGGCGCCTTCTTGAGGCAACATTCACAGC... |
Task1_train_34731 | Consider a variant on Chromosome 2. Determine its clinical classification and disease relevance. | Benign | CTTCCCCTGAAAAGCTGTTACCTCACCCTGGAAGTTACTATTTCTGGCAGTTTTTCCTAGGCCCCGGGGCCCTTACCTTGTGCACCTGAGGGGGTAGCTCATCCTCCGAGCCCTCTTCGGGCACGGGCTCAGGGTGCCTTGATGCCGACTGCCCATCTTCTGCCCACCCTCCAAGAGGCAGCCGAGAGAAATGAGAGGGAACCCTGGGCACTGTGCCAGGATCTGGAGAGACAAGTAAGAGTAAGCATACTCATAGAAGGAACACAAGAATGAGGAACAGGGCTGGGGGGCTGCTTGGGGGGTGAGTCTTTGGGCCTGTT... | CTTCCCCTGAAAAGCTGTTACCTCACCCTGGAAGTTACTATTTCTGGCAGTTTTTCCTAGGCCCCGGGGCCCTTACCTTGTGCACCTGAGGGGGTAGCTCATCCTCCGAGCCCTCTTCGGGCACGGGCTCAGGGTGCCTTGATGCCGACTGCCCATCTTCTGCCCACCCTCCAAGAGGCAGCCGAGAGAAATGAGAGGGAACCCTGGGCACTGTGCCAGGATCTGGAGAGACAAGTAAGAGTAAGCATACTCATAGAAGGAACACAAGAATGAGGAACAGGGCTGGGGGGCTGCTTGGGGGGTGAGTCTTTGGGCCTGTT... |
Task1_train_34732 | An alteration has been detected on Chromosome 2. Is it pathogenic, and if so, what disease is involved? | Benign | TATATCCAGAGGATTTTCTAAGCCTTGGACTGCAGCCCAGCTACATCTGCATTGAGAGAAACCTGCGCTAGCTTCTCCTCAGCTAAGGTTGAGAAAGATCTTTTCTTTTATGGCAGAAGAAGACCCTCGGGAAGCAGTCAGACTGCACTCACCTCAGACACACTGGAAAACAGTAAGAGAGGAGAGAAAGAAGCCTACTGAGGAAGAAATAAGAAAGATCTGCAGGGATGAAAAGGAAGCGCTGGGGCAGAATGAGGAATCTCCCAAACAGGGTTTGATTACTATCTGGCAACTGTCAGATCTGAGTTTCTGTCCTAAAA... | TATATCCAGAGGATTTTCTAAGCCTTGGACTGCAGCCCAGCTACATCTGCATTGAGAGAAACCTGCGCTAGCTTCTCCTCAGCTAAGGTTGAGAAAGATCTTTTCTTTTATGGCAGAAGAAGACCCTCGGGAAGCAGTCAGACTGCACTCACCTCAGACACACTGGAAAACAGTAAGAGAGGAGAGAAAGAAGCCTACTGAGGAAGAAATAAGAAAGATCTGCAGGGATGAAAAGGAAGCGCTGGGGCAGAATGAGGAATCTCCCAAACAGGGTTTGATTACTATCTGGCAACTGTCAGATCTGAGTTTCTGTCCTAAAA... |
Task1_train_34733 | A variant was discovered on Chromosome 2. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CCGTTCTCTGCCCTTTGCCCACTCAGTGTGAGTGCATCTCAGTCCACGTGGGGCAGGCCGGTGTGCAGTTGGCAATGCCTGCTGGGAGCTCTACTGCCTGGAACATAGGATTCAGTCTGATGGGCAGATGCCCAGTGACAAGACCATCAGGGGAGGGGGATGACTCCTTCAACACCTTTTTTAGTGAAACTGGGGCTGGGAAACATGTGCCCCAGGCGGTGTTTGTGGATCTGGAGCCCGCTGTGATGATCAGTCCCAGCCACAACCTTGTCCCTGGGTACCACAGCAAGTCCTACTCCATAACTGCAGAGCATGGTGTC... | CCGTTCTCTGCCCTTTGCCCACTCAGTGTGAGTGCATCTCAGTCCACGTGGGGCAGGCCGGTGTGCAGTTGGCAATGCCTGCTGGGAGCTCTACTGCCTGGAACATAGGATTCAGTCTGATGGGCAGATGCCCAGTGACAAGACCATCAGGGGAGGGGGATGACTCCTTCAACACCTTTTTTAGTGAAACTGGGGCTGGGAAACATGTGCCCCAGGCGGTGTTTGTGGATCTGGAGCCCGCTGTGATGATCAGTCCCAGCCACAACCTTGTCCCTGGGTACCACAGCAAGTCCTACTCCATAACTGCAGAGCATGGTGTC... |
Task1_train_34734 | Here is a genetic alteration on Chromosome 2. Based on the data, is it a benign variant or a cause of disease? | Benign | GACCCTGGTCTTCCTGACTTCTGTCTGTCCATCTCTGTCCTGCACTGGTCCCACACAATAGCGTTGGGGGTGACCAGGCAGTCTCAGCCCCTTGGTTATGAGCTTCATGTGAGCAGGTTCTCGGTTCTCACTCATTCATCTTCAAACCCCAGTGCCTCAGGGCACAGTGCCAGGCATTGATGGGGTCTTGGGGATTTGGGAGGGGGGGTTCAGCAAATGAGTCTGGAAAGAGCGCCTGAATAAACTGTTCATGGAGGGTTGTGCCAGGTCACTTGAAGGCTGAGGTCATTCGGGTATCAGGAGTTGAATTAAGAGCCTTC... | GACCCTGGTCTTCCTGACTTCTGTCTGTCCATCTCTGTCCTGCACTGGTCCCACACAATAGCGTTGGGGGTGACCAGGCAGTCTCAGCCCCTTGGTTATGAGCTTCATGTGAGCAGGTTCTCGGTTCTCACTCATTCATCTTCAAACCCCAGTGCCTCAGGGCACAGTGCCAGGCATTGATGGGGTCTTGGGGATTTGGGAGGGGGGGTTCAGCAAATGAGTCTGGAAAGAGCGCCTGAATAAACTGTTCATGGAGGGTTGTGCCAGGTCACTTGAAGGCTGAGGTCATTCGGGTATCAGGAGTTGAATTAAGAGCCTTC... |
Task1_train_34735 | Located on Chromosome 2, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | AGGGCTGGGCCCGGGTCACTTTCACCTCTGAGAGAGGTGGCCTCTCTCTCTCTCTCCCTGCTACCCAGTACCCTCACTTGGCCTGGAGGCAGCCATTGAGAAACTGTGTTCACATTGCCTTGTTGGAACCTCAGTGTGGGACCCCTCCTTGGGGAGCAGTGGGGTACAGCGGGAAGGGGGCACACTGCCATCCTGATCACCACACCTGCTGAGTACTCCTCTTCTGCCTGGCTCATCCCCACTCCCAGTCCCCCACAATTCTTCAGACAGGCAGCAGCTGGGGCTCACAAGGCTCCTCAGCTTTCTCTTCCCAGGTGAAT... | AGGGCTGGGCCCGGGTCACTTTCACCTCTGAGAGAGGTGGCCTCTCTCTCTCTCTCCCTGCTACCCAGTACCCTCACTTGGCCTGGAGGCAGCCATTGAGAAACTGTGTTCACATTGCCTTGTTGGAACCTCAGTGTGGGACCCCTCCTTGGGGAGCAGTGGGGTACAGCGGGAAGGGGGCACACTGCCATCCTGATCACCACACCTGCTGAGTACTCCTCTTCTGCCTGGCTCATCCCCACTCCCAGTCCCCCACAATTCTTCAGACAGGCAGCAGCTGGGGCTCACAAGGCTCCTCAGCTTTCTCTTCCCAGGTGAAT... |
Task1_train_34736 | A variant has been detected on Chromosome 2. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CCAGGCTTCTCTGCTGGCCATATTATTGAGAAAATGATAACAACAAGAGAAGTTAGTATTTATGATCAGTTACTCTATGGCAGACACTTTACATGCCTCGTAATTGTCACAGCAAGCATCCTGTGGGCGTGGGATTATTTTCCTTGATTTACAGATTAGAAATGGAGCTTCTGAGAGAGTAAATGACTTGCCCAAGGTCAGGCAGATACTGTCTCTTGCCCCTTCAAAAGCTCTCACCACTTAATTGACCTGAAGGAGTATACAGAAGACCTACGACCCTGTCCCCCGATGGCAGGTGGGAAGAGGGGCCAGGAAGCCGA... | CCAGGCTTCTCTGCTGGCCATATTATTGAGAAAATGATAACAACAAGAGAAGTTAGTATTTATGATCAGTTACTCTATGGCAGACACTTTACATGCCTCGTAATTGTCACAGCAAGCATCCTGTGGGCGTGGGATTATTTTCCTTGATTTACAGATTAGAAATGGAGCTTCTGAGAGAGTAAATGACTTGCCCAAGGTCAGGCAGATACTGTCTCTTGCCCCTTCAAAAGCTCTCACCACTTAATTGACCTGAAGGAGTATACAGAAGACCTACGACCCTGTCCCCCGATGGCAGGTGGGAAGAGGGGCCAGGAAGCCGA... |
Task1_train_34737 | A variant was discovered on Chromosome 2. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CTCTTCTTTCTCTTGCCAGGAGTCCCAGGAAAGCTAGCTCCTCCAGAGGTACCCCAGACCTACCAGGACACGGCGCTGGTGCTGTGGAAGCCGGGAGACAGCCGGGCACCTTGCACGTATACGCTGGAGCGGCGAGTGGATGGTGAGGATGGGGCAGCTGGAGGGTTGGGGGAGCGGCAGGGGGAGGGTAGAGGAGTCTGGTAAGGCCAGTGCCCTCCCAGGCTCCACAGATAGCACCGTGGGAGCTGGGGCCACCGCTTCTGTGACCTCAGCCCCTCCCCCATACTGCCTATAGGGGAGTCTGTGTGGCACCCTGTGAG... | CTCTTCTTTCTCTTGCCAGGAGTCCCAGGAAAGCTAGCTCCTCCAGAGGTACCCCAGACCTACCAGGACACGGCGCTGGTGCTGTGGAAGCCGGGAGACAGCCGGGCACCTTGCACGTATACGCTGGAGCGGCGAGTGGATGGTGAGGATGGGGCAGCTGGAGGGTTGGGGGAGCGGCAGGGGGAGGGTAGAGGAGTCTGGTAAGGCCAGTGCCCTCCCAGGCTCCACAGATAGCACCGTGGGAGCTGGGGCCACCGCTTCTGTGACCTCAGCCCCTCCCCCATACTGCCTATAGGGGAGTCTGTGTGGCACCCTGTGAG... |
Task1_train_34738 | A genomic variant on Chromosome 2 is under review. What is the biological outcome — benign or pathogenic? | Benign | TAGCTGGGATTATAGGCACCCACAGCCATACCCAGCTAATTTTTGTCTTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTTAAACTCCTGACCTCAAGTGATCTGCCGTCCTTGGTCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCTTGCCTGGCCACAGCCCTTCTCTTCTAAGTAGCCCCACTCATTGCTCAAGTCACGTTCAGTGTCTCCACCTCCAGGGAAGTGCTTCCAGGTCCAAACACCTTTCATCTGAGTTCCCAGCACCCGTACAGATCTCTGTCATTACACATATGCCACATTT... | TAGCTGGGATTATAGGCACCCACAGCCATACCCAGCTAATTTTTGTCTTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTTAAACTCCTGACCTCAAGTGATCTGCCGTCCTTGGTCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCTTGCCTGGCCACAGCCCTTCTCTTCTAAGTAGCCCCACTCATTGCTCAAGTCACGTTCAGTGTCTCCACCTCCAGGGAAGTGCTTCCAGGTCCAAACACCTTTCATCTGAGTTCCCAGCACCCGTACAGATCTCTGTCATTACACATATGCCACATTT... |
Task1_train_34739 | This variant is located on Chromosome 2. Evaluate its biological effect and specify any disease association. | Benign | TTATAGGCACCCACAGCCATACCCAGCTAATTTTTGTCTTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTTAAACTCCTGACCTCAAGTGATCTGCCGTCCTTGGTCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCTTGCCTGGCCACAGCCCTTCTCTTCTAAGTAGCCCCACTCATTGCTCAAGTCACGTTCAGTGTCTCCACCTCCAGGGAAGTGCTTCCAGGTCCAAACACCTTTCATCTGAGTTCCCAGCACCCGTACAGATCTCTGTCATTACACATATGCCACATTTCAGAGTGCT... | TTATAGGCACCCACAGCCATACCCAGCTAATTTTTGTCTTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTTAAACTCCTGACCTCAAGTGATCTGCCGTCCTTGGTCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCTTGCCTGGCCACAGCCCTTCTCTTCTAAGTAGCCCCACTCATTGCTCAAGTCACGTTCAGTGTCTCCACCTCCAGGGAAGTGCTTCCAGGTCCAAACACCTTTCATCTGAGTTCCCAGCACCCGTACAGATCTCTGTCATTACACATATGCCACATTTCAGAGTGCT... |
Task1_train_34740 | A variant affecting Chromosome 2 has been observed. Determine if it's benign or associated with disease. | Benign | CTGTCATGCCAACCTAGACACCTCATGCTTCTGTCTCCCCCACCCCACTCTGTTTTACATCTTTTATAAATGTGCCAAACTGTGTGGCCTCTGCCAGGAATGGTGGTCTTTGGTGGCTGGCACTTTCATGGGCCAGGTACAAGCACTACAGCCCTCGGTCCCCAGTGTCGCTCACTGCACAGGGGCTCCAGGCAAGGTCTGCCCCCCCACATCACTCAGAGAGGCAAGGAAATGAGCTGTAGCACTTTTATTGTTCCTTGTCTCTCTACCCCTGCCCAGGGTAAGGGCAAACGCCTTCCAAGCTGTCCAAGGGCACCCGC... | CTGTCATGCCAACCTAGACACCTCATGCTTCTGTCTCCCCCACCCCACTCTGTTTTACATCTTTTATAAATGTGCCAAACTGTGTGGCCTCTGCCAGGAATGGTGGTCTTTGGTGGCTGGCACTTTCATGGGCCAGGTACAAGCACTACAGCCCTCGGTCCCCAGTGTCGCTCACTGCACAGGGGCTCCAGGCAAGGTCTGCCCCCCCACATCACTCAGAGAGGCAAGGAAATGAGCTGTAGCACTTTTATTGTTCCTTGTCTCTCTACCCCTGCCCAGGGTAAGGGCAAACGCCTTCCAAGCTGTCCAAGGGCACCCGC... |
Task1_train_34741 | A change on Chromosome 2 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GAAGTAAAAATGGGGGACACTCAAGCAGACTTGCTAGTGATGTCGCCCGTAGGCAGTCAGTGGATTCAAGGGACTGGAGTGGTCACGGGGCCCACACTTAGGCGGGCAGAGGGAGCCACGGCAGACAGTGTAGCCAGTAGGGTCACAGTTAGAGTGGTCAGTGGGGTGGTGTGCAGGCGGGCAGACAGCAGTGACCACAATGGCAAAGGCATGCTCTTGGTAGCAGAGTCAGTGGTTGGCTGAGCCTTGGGCAGTCAGGGGCCACACCCAGGCAGAGGACTCTGGGGCCACACAGGGCCTATGAGTCAGGGGGATCACAC... | GAAGTAAAAATGGGGGACACTCAAGCAGACTTGCTAGTGATGTCGCCCGTAGGCAGTCAGTGGATTCAAGGGACTGGAGTGGTCACGGGGCCCACACTTAGGCGGGCAGAGGGAGCCACGGCAGACAGTGTAGCCAGTAGGGTCACAGTTAGAGTGGTCAGTGGGGTGGTGTGCAGGCGGGCAGACAGCAGTGACCACAATGGCAAAGGCATGCTCTTGGTAGCAGAGTCAGTGGTTGGCTGAGCCTTGGGCAGTCAGGGGCCACACCCAGGCAGAGGACTCTGGGGCCACACAGGGCCTATGAGTCAGGGGGATCACAC... |
Task1_train_34742 | A mutation on Chromosome 2 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GAGGGCTGGCTGGTGACAGGGTCTTCCTGGTCAGTGGAAAGTAGGGTCCCGCCTTTTGGCTGGCTTGGGCAAGGCAGAGGTGCTCCCAGGCTCCAACCTCTCTCTCCTTCCTGTCGTCACGTGCCAGACTCACACATCCTTGGGGCTCAGCCCCATGGGCCCACCTTTGCCCTGGCCAGTGGGGAGTACTCCTGAAACCTCAGGTGGCCCTGACCTGAGTGACAGCCTCTCCTCAGGGGGTGTTGTGACCCAGCCCCTGCTTCATAAGGTTAAGGTAAGCAGCGTCCTCCGCTGCCTTGTGCCTGCGGTTGGGTGTCTCT... | GAGGGCTGGCTGGTGACAGGGTCTTCCTGGTCAGTGGAAAGTAGGGTCCCGCCTTTTGGCTGGCTTGGGCAAGGCAGAGGTGCTCCCAGGCTCCAACCTCTCTCTCCTTCCTGTCGTCACGTGCCAGACTCACACATCCTTGGGGCTCAGCCCCATGGGCCCACCTTTGCCCTGGCCAGTGGGGAGTACTCCTGAAACCTCAGGTGGCCCTGACCTGAGTGACAGCCTCTCCTCAGGGGGTGTTGTGACCCAGCCCCTGCTTCATAAGGTTAAGGTAAGCAGCGTCCTCCGCTGCCTTGTGCCTGCGGTTGGGTGTCTCT... |
Task1_train_34743 | Chromosome 2 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AGGAAAAAGAAAACCGTCTGCCTGCTGCATTTACAAAAAGGAAAACAGAAAAAAAGAAGAAACTATATCCTGTTTTTTTTTTTTTTTTAACTCTAAAAGTCAGGAAATGCAATCTCTGTAACTGTGCTTAAACATACTCATTATTTTTTCATAACTTGAAGGCTTGTTGTGTTGGGGATTTTTTGGCTGATATTTCAGACACTACATAAAACCTAATGAGCCCTCACTGCAGTATTGGATTGTGGTGCTGCCTCTGCCAGCAAGTGTAGCTGTTGAGTGAGATGCTTGGGGAGTTGGCTTGGTTTATCCTTCCCGGCTGA... | AGGAAAAAGAAAACCGTCTGCCTGCTGCATTTACAAAAAGGAAAACAGAAAAAAAGAAGAAACTATATCCTGTTTTTTTTTTTTTTTTAACTCTAAAAGTCAGGAAATGCAATCTCTGTAACTGTGCTTAAACATACTCATTATTTTTTCATAACTTGAAGGCTTGTTGTGTTGGGGATTTTTTGGCTGATATTTCAGACACTACATAAAACCTAATGAGCCCTCACTGCAGTATTGGATTGTGGTGCTGCCTCTGCCAGCAAGTGTAGCTGTTGAGTGAGATGCTTGGGGAGTTGGCTTGGTTTATCCTTCCCGGCTGA... |
Task1_train_34744 | Chromosome 2 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | ACTGCAATTTGTAACTACTATAAGTAACACTGTGAACACTTGCATAAAAATCTTTGGCCATATGGGTAAACCTAGGAATAGAATGGCTAGATGGTAGGTGTATGTTTCAAGAGACTGCCAAGCTGTTTTCTAAAGTCACAATGTAACATTTTACATTGTGACTCACCAGCAGTGCATGAAAGTTCCACTTGCTCCAGTCTCAGCAGTATTTGATTTATGAATCTTAAATTTTAGCCATTTTAATGGGTATGCAGTTTGTCATTGTGAATTTTAGTTGCATTTCCCTGATGACTAACGATGTTGAGGATCTTTTCAAGTGC... | ACTGCAATTTGTAACTACTATAAGTAACACTGTGAACACTTGCATAAAAATCTTTGGCCATATGGGTAAACCTAGGAATAGAATGGCTAGATGGTAGGTGTATGTTTCAAGAGACTGCCAAGCTGTTTTCTAAAGTCACAATGTAACATTTTACATTGTGACTCACCAGCAGTGCATGAAAGTTCCACTTGCTCCAGTCTCAGCAGTATTTGATTTATGAATCTTAAATTTTAGCCATTTTAATGGGTATGCAGTTTGTCATTGTGAATTTTAGTTGCATTTCCCTGATGACTAACGATGTTGAGGATCTTTTCAAGTGC... |
Task1_train_34745 | This is a variant located on Chromosome 2. Is this mutation a likely cause of disease or not? | Benign | TCGTAGTGTCCCCACCTAGCACTGGGGGAAGATTCAAGGAAGAAATCTAAAAGGAAAGAAGAAAGTGACTCCTTAAGTAGGAGGAAAAAGAAACCCAAACAAGTTTTGCATACAAAAAATCACAAACAACTCCTCCAAGTGGCCCTGGTATTTGTTTTAATCCAACTCCCTTTGTATTAAAATGTTGAAGGAGAAAAGGGCATAGGATGGGGGAGAAAGGAGGGCCAACTATATTGTTTTGCCCTGTTCCAAGTCCTCTTCAGCAATGACTTGACAGCTGCTCATCATTTTGAGTTTTTCAACTATGTGGTAATTAATAT... | TCGTAGTGTCCCCACCTAGCACTGGGGGAAGATTCAAGGAAGAAATCTAAAAGGAAAGAAGAAAGTGACTCCTTAAGTAGGAGGAAAAAGAAACCCAAACAAGTTTTGCATACAAAAAATCACAAACAACTCCTCCAAGTGGCCCTGGTATTTGTTTTAATCCAACTCCCTTTGTATTAAAATGTTGAAGGAGAAAAGGGCATAGGATGGGGGAGAAAGGAGGGCCAACTATATTGTTTTGCCCTGTTCCAAGTCCTCTTCAGCAATGACTTGACAGCTGCTCATCATTTTGAGTTTTTCAACTATGTGGTAATTAATAT... |
Task1_train_34746 | A variant affecting Chromosome 2 has been observed. Determine if it's benign or associated with disease. | Benign | TCAGTAACTATTTTGTCATTATTATCAATACTTAGCCCAGTACCTGGCCAGTAGCAGGTGCTCAATAAATGCTTTTAAATGAATGAATGATCAGTCAATGTGGTGGCTAAGAAAGGAGAATGTGGCTACATATGGAAGAAGCTGTGTTTTGACCAGATAGATGATGGTCCCATTCACCTTGATAAATAATGTTGGAAGAGGGACAACTTTAAGGGAGAATTTAATGCATTCGGTTTGGAGACGTGTAGTTTGAGGTGTCTTAGAGCTGTCACTGTAGAGCTGTCAATTGGGCATTTGGAGATATGGGCCTGGAACCTCAG... | TCAGTAACTATTTTGTCATTATTATCAATACTTAGCCCAGTACCTGGCCAGTAGCAGGTGCTCAATAAATGCTTTTAAATGAATGAATGATCAGTCAATGTGGTGGCTAAGAAAGGAGAATGTGGCTACATATGGAAGAAGCTGTGTTTTGACCAGATAGATGATGGTCCCATTCACCTTGATAAATAATGTTGGAAGAGGGACAACTTTAAGGGAGAATTTAATGCATTCGGTTTGGAGACGTGTAGTTTGAGGTGTCTTAGAGCTGTCACTGTAGAGCTGTCAATTGGGCATTTGGAGATATGGGCCTGGAACCTCAG... |
Task1_train_34747 | The following genetic variant occurs on Chromosome 2. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CTTGTCTTTGTCCATTTACAACTCTCCTCCGTTTCTATCCCTTTTGCGGAGAAGAGCACCCAAAATCAGCCTAGACTCACTTTTGCAAGATTTGACTTTAGGACTGAACTCATCTCTGTCTCCAGTTAGGTGTAGTAAGTCTCCAAGTCTCCAAAAGATCCAGCTAAATCAACATTTACACTCTTATGTAACATCTGTTCTGAGAGTGAAGTTCGTGGAATTGAATAACCTTATAAATGAACTGAAACACAGGCCTCGGGATTTTTAAACATGTGTGTACAGACATATCCAAAAAATTCAGCATATGGGCAACGAGAATT... | CTTGTCTTTGTCCATTTACAACTCTCCTCCGTTTCTATCCCTTTTGCGGAGAAGAGCACCCAAAATCAGCCTAGACTCACTTTTGCAAGATTTGACTTTAGGACTGAACTCATCTCTGTCTCCAGTTAGGTGTAGTAAGTCTCCAAGTCTCCAAAAGATCCAGCTAAATCAACATTTACACTCTTATGTAACATCTGTTCTGAGAGTGAAGTTCGTGGAATTGAATAACCTTATAAATGAACTGAAACACAGGCCTCGGGATTTTTAAACATGTGTGTACAGACATATCCAAAAAATTCAGCATATGGGCAACGAGAATT... |
Task1_train_34748 | This mutation on Chromosome 2 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | CAGTTTTCTCTAAAAGTACCCAAAGAGACTCTCTAAAGGTTATTCAAATAAGAAAGACTCAAGTAACAAGTGAGAGTTAGAAACAACACAGTTAAAATGTATATAACCACAATCCATACCTCAAATGTGTATTTTTCTCTATTATTAAAGAGCATTAATATGGTCATCTGGAAAGTGGAAACTTGCAATATGTGCTTCCGTGTATTAGAGCCAGTTACTTGTGCACCTCCAACACCAACTTCAGATCCATCTTCCTGTTTCATTTTTAAAAAAATATAAACAAAGACACAATCATTTCCTGGTAACATTAATGTATGTAT... | CAGTTTTCTCTAAAAGTACCCAAAGAGACTCTCTAAAGGTTATTCAAATAAGAAAGACTCAAGTAACAAGTGAGAGTTAGAAACAACACAGTTAAAATGTATATAACCACAATCCATACCTCAAATGTGTATTTTTCTCTATTATTAAAGAGCATTAATATGGTCATCTGGAAAGTGGAAACTTGCAATATGTGCTTCCGTGTATTAGAGCCAGTTACTTGTGCACCTCCAACACCAACTTCAGATCCATCTTCCTGTTTCATTTTTAAAAAAATATAAACAAAGACACAATCATTTCCTGGTAACATTAATGTATGTAT... |
Task1_train_34749 | Assess the clinical impact of this variant found on Chromosome 2. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TTTAAGACACAGTTTTGCTCTTGTCTCCCAGGCTGGAGTGCAGTGGTGTGATCTTGGTTTACTGCAACCTCTGCCTCCTGAGTTCAAGCGATTCTCCTGCTTCAGCCTCCCGAGTAGCTGGGATTGTAGGAGTGTGCCACCACACAGGCTAATTTTTTTTTGTATTTTTAGTAGTGACGGGGTTTCACCATGTTGGCCAAGCTGGTCTCACACTCCTGACCTCAGGTGATCCACCAGCCTCAGCCTCCCAAATTGTTGGGATTACAGCATGAGCCACCGTGCCTGGCCTGTTTCTATTTTTAAGTGTTCAATAGAATTTT... | TTTAAGACACAGTTTTGCTCTTGTCTCCCAGGCTGGAGTGCAGTGGTGTGATCTTGGTTTACTGCAACCTCTGCCTCCTGAGTTCAAGCGATTCTCCTGCTTCAGCCTCCCGAGTAGCTGGGATTGTAGGAGTGTGCCACCACACAGGCTAATTTTTTTTTGTATTTTTAGTAGTGACGGGGTTTCACCATGTTGGCCAAGCTGGTCTCACACTCCTGACCTCAGGTGATCCACCAGCCTCAGCCTCCCAAATTGTTGGGATTACAGCATGAGCCACCGTGCCTGGCCTGTTTCTATTTTTAAGTGTTCAATAGAATTTT... |
Task1_train_34750 | Given this variant on Chromosome 2, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TGGCAGGAAGGATTGGATCCTTTGAGAGTTCCATTGTTCTGGGTGGACTGCACAAATTTAAATGCAGCAGCAATTTTTCTGCAATGAAAATGGAAGTTTTAATCATAGCTCAGTGTTTGTAATTTACATATAAAAATGAATGGCAACTGACAAAACGATTACTGCACAATGAAATATTTCACATGCTGTGAATTAATCAAAAATAAAACCCTGTTTTCTTTCGGAAATCAGAAATTGGGATTTAGTGAAGGTGCTTCAAACGTTGTTGTCTCATGAGAAAATGATGACAGTACGAAGTTATTCCAGATTACTTGTTTTTT... | TGGCAGGAAGGATTGGATCCTTTGAGAGTTCCATTGTTCTGGGTGGACTGCACAAATTTAAATGCAGCAGCAATTTTTCTGCAATGAAAATGGAAGTTTTAATCATAGCTCAGTGTTTGTAATTTACATATAAAAATGAATGGCAACTGACAAAACGATTACTGCACAATGAAATATTTCACATGCTGTGAATTAATCAAAAATAAAACCCTGTTTTCTTTCGGAAATCAGAAATTGGGATTTAGTGAAGGTGCTTCAAACGTTGTTGTCTCATGAGAAAATGATGACAGTACGAAGTTATTCCAGATTACTTGTTTTTT... |
Task1_train_34751 | Chromosome 2 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AGCAGGCAACTGTAGCACGGACATCCCCAGTGCCTTCTGTCGTCGAAGAAAGCTAATCACTGTATGAATGATCTTAATTAAATTTGAATGCATTGCTAACTGAATGCTGTGGGAAAATACCGCGTCCTTACTGGCCGCTCTTCCCATAGTACTCAGTAGCAATACATTCAAATTCAATTAAGATAATTCATAGAGTGATTAGCTTCATTATATGGTGAGACTCTGGGGACTGTCCTCTTGCCAACACTGTATGAGTGGTCTCGGTAAGATAGACACGTTCTTCTGTGCATTTTCTCTTTTAGTGGACACAAGAAATAACT... | AGCAGGCAACTGTAGCACGGACATCCCCAGTGCCTTCTGTCGTCGAAGAAAGCTAATCACTGTATGAATGATCTTAATTAAATTTGAATGCATTGCTAACTGAATGCTGTGGGAAAATACCGCGTCCTTACTGGCCGCTCTTCCCATAGTACTCAGTAGCAATACATTCAAATTCAATTAAGATAATTCATAGAGTGATTAGCTTCATTATATGGTGAGACTCTGGGGACTGTCCTCTTGCCAACACTGTATGAGTGGTCTCGGTAAGATAGACACGTTCTTCTGTGCATTTTCTCTTTTAGTGGACACAAGAAATAACT... |
Task1_train_34752 | This sequence change occurs on Chromosome 2. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GTAGCACGGACATCCCCAGTGCCTTCTGTCGTCGAAGAAAGCTAATCACTGTATGAATGATCTTAATTAAATTTGAATGCATTGCTAACTGAATGCTGTGGGAAAATACCGCGTCCTTACTGGCCGCTCTTCCCATAGTACTCAGTAGCAATACATTCAAATTCAATTAAGATAATTCATAGAGTGATTAGCTTCATTATATGGTGAGACTCTGGGGACTGTCCTCTTGCCAACACTGTATGAGTGGTCTCGGTAAGATAGACACGTTCTTCTGTGCATTTTCTCTTTTAGTGGACACAAGAAATAACTCTCAGGGTGAC... | GTAGCACGGACATCCCCAGTGCCTTCTGTCGTCGAAGAAAGCTAATCACTGTATGAATGATCTTAATTAAATTTGAATGCATTGCTAACTGAATGCTGTGGGAAAATACCGCGTCCTTACTGGCCGCTCTTCCCATAGTACTCAGTAGCAATACATTCAAATTCAATTAAGATAATTCATAGAGTGATTAGCTTCATTATATGGTGAGACTCTGGGGACTGTCCTCTTGCCAACACTGTATGAGTGGTCTCGGTAAGATAGACACGTTCTTCTGTGCATTTTCTCTTTTAGTGGACACAAGAAATAACTCTCAGGGTGAC... |
Task1_train_34753 | A mutation found on Chromosome 2 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | ACTTTAAGTTATTTATATTCTGCTGGCTATTTCTTTCATGGGATTATGAGACCCTGGAGGGGGAAAACACATCTTACTCATCTTACTCACCCATACCACCTAGTAGCATACTTTACAAAGAGTAGAGGGAGTCTGGAAGTACTTACTGAATTGAATTTGCAGAACCCAGTTATAGGTCACGTCTTCAAGTTGGAAGTTATTTTTTTAAGTTGGAGGGACCCAGCTCTGGATATTGCAAATATATACACAAGGCAGCTTGGTTTTAAAATGAGGTTGATGACTAGTAATACCGACTGACAGAACTTTATGCATGCAAGGAG... | ACTTTAAGTTATTTATATTCTGCTGGCTATTTCTTTCATGGGATTATGAGACCCTGGAGGGGGAAAACACATCTTACTCATCTTACTCACCCATACCACCTAGTAGCATACTTTACAAAGAGTAGAGGGAGTCTGGAAGTACTTACTGAATTGAATTTGCAGAACCCAGTTATAGGTCACGTCTTCAAGTTGGAAGTTATTTTTTTAAGTTGGAGGGACCCAGCTCTGGATATTGCAAATATATACACAAGGCAGCTTGGTTTTAAAATGAGGTTGATGACTAGTAATACCGACTGACAGAACTTTATGCATGCAAGGAG... |
Task1_train_34754 | This alteration on Chromosome 2 may affect genome function. Does it lead to a disease or is it benign? | Benign | GGCAGCACCTTATTTACATAAAATGTCCACATCAATGTGACTGACAGGAGCAGCTATGATTTAGTAACGGAGTTTTCATCTCTAGAATGACTTGAAACTCTCTTGAGCAATATAAAATTCTAGTTGATTTCTTCTGGCAAATATCCTCTAATTTAATGCATGTAGGAATTCTATCCATTTAAAAGCTTCTGAAAATTTCATATTAATTTGCCAAGTATAGGGTATGCATAGAAAGGAAATATGAAAAGAAACAACATATAGGCCAGGCTCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGGA... | GGCAGCACCTTATTTACATAAAATGTCCACATCAATGTGACTGACAGGAGCAGCTATGATTTAGTAACGGAGTTTTCATCTCTAGAATGACTTGAAACTCTCTTGAGCAATATAAAATTCTAGTTGATTTCTTCTGGCAAATATCCTCTAATTTAATGCATGTAGGAATTCTATCCATTTAAAAGCTTCTGAAAATTTCATATTAATTTGCCAAGTATAGGGTATGCATAGAAAGGAAATATGAAAAGAAACAACATATAGGCCAGGCTCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGGA... |
Task1_train_34755 | An alteration has been detected on Chromosome 2. Is it pathogenic, and if so, what disease is involved? | Benign | GTTAACCTGTGAATTTACAGCTAGTTACGCTAAGGCTAAGGTTAAAAAGGTAAATCATTTTAAAGTAGATTTAAAGAAAAATATTAACCCAATGGTATACCAAGATAGTAAAACTATTAAAGGTTTTATGCAAACATTGCAACTAAGATATCCTGCTCTTTGTTTGTTTACTTGTTTGTCTGAATAAAGGGTTAATGAAGCCTCTCTTTCACTAGAATGTTAGGTGTGTTACAATGCAGCACTGTTTTTGACACAAGGTAAACTAAGGCCCGTGGGGCCAAATCTAGCCTGCAGCCAATTTTGCAAATAAAGTTCTATTG... | GTTAACCTGTGAATTTACAGCTAGTTACGCTAAGGCTAAGGTTAAAAAGGTAAATCATTTTAAAGTAGATTTAAAGAAAAATATTAACCCAATGGTATACCAAGATAGTAAAACTATTAAAGGTTTTATGCAAACATTGCAACTAAGATATCCTGCTCTTTGTTTGTTTACTTGTTTGTCTGAATAAAGGGTTAATGAAGCCTCTCTTTCACTAGAATGTTAGGTGTGTTACAATGCAGCACTGTTTTTGACACAAGGTAAACTAAGGCCCGTGGGGCCAAATCTAGCCTGCAGCCAATTTTGCAAATAAAGTTCTATTG... |
Task1_train_34756 | This mutation occurs on Chromosome 2. Does this change lead to a known medical condition, or is it benign? | Benign | ATGCTCTGCAGCCCTTCCTAACCTCCTGCCAGTTCCTTGACTTCATTTCCTGCTCTGCCCCTCTCTCTCTTCTCTCCAGCTACAATCGATGGTGATGGCGTTTATCACCACATGACATACTGGATATTTACTTGCTGATCTGTTAGATGGTCTGTGTCCTCTCTGAAGCTCTAGGAGGGCAGAGACTGGGCTCTGGTCCCTGCTGTATCCCCAGCACCTGAAACAAGGCCTAGAACATAGCAGGCACTTAACAATACCAATTAGTTGAATAAGTAAACGATGGATGAATGGATGAGTAAATAAACTGTTTTTGCAGGCAT... | ATGCTCTGCAGCCCTTCCTAACCTCCTGCCAGTTCCTTGACTTCATTTCCTGCTCTGCCCCTCTCTCTCTTCTCTCCAGCTACAATCGATGGTGATGGCGTTTATCACCACATGACATACTGGATATTTACTTGCTGATCTGTTAGATGGTCTGTGTCCTCTCTGAAGCTCTAGGAGGGCAGAGACTGGGCTCTGGTCCCTGCTGTATCCCCAGCACCTGAAACAAGGCCTAGAACATAGCAGGCACTTAACAATACCAATTAGTTGAATAAGTAAACGATGGATGAATGGATGAGTAAATAAACTGTTTTTGCAGGCAT... |
Task1_train_34757 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CCTGGGTAACAGAGTGAGGTTCTGTCTCAAAACAACAAAACAAAACACCCATTAAACATCTGCATATATTTTCTAGACCTTATATTTGTCAAACAGCTTCTGGATCCATCATCTTATTTAACGCTTAAAACAGCTGTGGTTAGAACTTCGGGTCACACCATTCCAAAGGATGGTAGGAGAACTGGGGCTCAGTTCTGGGCTGTGATTTATCTGCCATCCTTGTTCTTTTGTTCTCTGTAGAGCCTTCTCCTCTCTAAAACCTCATGTCCTAAGTGAGCCTTTGTTCTCCACCCTCTACTTCTTCCTCTTTTGCTGAGATG... | CCTGGGTAACAGAGTGAGGTTCTGTCTCAAAACAACAAAACAAAACACCCATTAAACATCTGCATATATTTTCTAGACCTTATATTTGTCAAACAGCTTCTGGATCCATCATCTTATTTAACGCTTAAAACAGCTGTGGTTAGAACTTCGGGTCACACCATTCCAAAGGATGGTAGGAGAACTGGGGCTCAGTTCTGGGCTGTGATTTATCTGCCATCCTTGTTCTTTTGTTCTCTGTAGAGCCTTCTCCTCTCTAAAACCTCATGTCCTAAGTGAGCCTTTGTTCTCCACCCTCTACTTCTTCCTCTTTTGCTGAGATG... |
Task1_train_34758 | This alteration on Chromosome 2 may affect genome function. Does it lead to a disease or is it benign? | Benign | CAAAAGATTGGAGCACTTCATTGCATGCAAATTGTACCTTAGGAATCGATCCAAAAAAGCCAAAAATAATCTTAATGATATCTTTTTAAGAGTTACATAAATGTGAGATTTACAAAAGTTTGTTAAACCTTTAGTATTTGTTTTCCCAATCGTTTCGAGCTATTCCCAGTTATAGTGGAGGAAAAAGATTATCGCAATGGTAAATAAATTTATGTTTATAGATTGAACATTTTTAAAGTTTTTTTTTTTTGCCACCCCCTCCTTTTTCCTATGTCTTCAGGGAATAAGTGGATTGCCAGGATTTTCTGGTTCTCCTGGAC... | CAAAAGATTGGAGCACTTCATTGCATGCAAATTGTACCTTAGGAATCGATCCAAAAAAGCCAAAAATAATCTTAATGATATCTTTTTAAGAGTTACATAAATGTGAGATTTACAAAAGTTTGTTAAACCTTTAGTATTTGTTTTCCCAATCGTTTCGAGCTATTCCCAGTTATAGTGGAGGAAAAAGATTATCGCAATGGTAAATAAATTTATGTTTATAGATTGAACATTTTTAAAGTTTTTTTTTTTTGCCACCCCCTCCTTTTTCCTATGTCTTCAGGGAATAAGTGGATTGCCAGGATTTTCTGGTTCTCCTGGAC... |
Task1_train_34759 | A mutation on Chromosome 2 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | ATTACTCAAGTTTGAAGGAAACAGCAATTAAAAAGTTCTTGGCGCAATTAGACTTTGCCATTTATGCACAATTTGAGAAACAGTATTCTAATCCTGTTTTTAATTAAGATAATGGTTTTTTGGTCTTCAGCCTCATGACCCAGTAGCCATAAGGAATTCGGGTTACTTTGTCTAGATTTACCATTGCAAGGTTGGAAGCGAGAAACAGGAAAAATATCTGAATAGGCTCTTCTAGAACAACTAAGAATAATAAGAAACTTTGTATGTCTTTTAGGGTGAGCAGGGGTTTCCAGGACTCCCAGGGACACTGGGCTACCCAG... | ATTACTCAAGTTTGAAGGAAACAGCAATTAAAAAGTTCTTGGCGCAATTAGACTTTGCCATTTATGCACAATTTGAGAAACAGTATTCTAATCCTGTTTTTAATTAAGATAATGGTTTTTTGGTCTTCAGCCTCATGACCCAGTAGCCATAAGGAATTCGGGTTACTTTGTCTAGATTTACCATTGCAAGGTTGGAAGCGAGAAACAGGAAAAATATCTGAATAGGCTCTTCTAGAACAACTAAGAATAATAAGAAACTTTGTATGTCTTTTAGGGTGAGCAGGGGTTTCCAGGACTCCCAGGGACACTGGGCTACCCAG... |
Task1_train_34760 | This mutation is located on Chromosome 2. Is it associated with a disease or is it a benign polymorphism? | Benign | ATATTGGCTAAAATACAATAACATTTGACCGCAGAGATCATGAATACACTAGAGTTATTTTACGGCCACTCCTAGCTGAAATCCTTGCACTGCTGTACATGCACCCAATGCCACCCATCCTATGACTTATCTTCAGCATCAGCTTTTTTAGCATCTGTTTTTTAATTACTATTCATCAATAAGATTTCTCTCTTAGATGGCTCAGCACTGAAACATGTTTTTAAATGGCAGAATAACCAAAAGGGACAAATTAATAAAAATCAATGTAAGTAAAAAAATCAGTAATTCATAAAATTTGACATGGCTCTAATTAATACAGG... | ATATTGGCTAAAATACAATAACATTTGACCGCAGAGATCATGAATACACTAGAGTTATTTTACGGCCACTCCTAGCTGAAATCCTTGCACTGCTGTACATGCACCCAATGCCACCCATCCTATGACTTATCTTCAGCATCAGCTTTTTTAGCATCTGTTTTTTAATTACTATTCATCAATAAGATTTCTCTCTTAGATGGCTCAGCACTGAAACATGTTTTTAAATGGCAGAATAACCAAAAGGGACAAATTAATAAAAATCAATGTAAGTAAAAAAATCAGTAATTCATAAAATTTGACATGGCTCTAATTAATACAGG... |
Task1_train_34761 | Given this context: Chromosome 2 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CATAAGGATACCTACATTACACTTTTTCTGTAAAGTTCTAAACTTTCGTCTCTGACTCATTAGAGTGTTTACCTTTTGAGAGAGGAAAAAGAGTTGGATCAGGGATGGTCCACAGGGACTCATCAAGTATAACTGTAGTGTGTTCTTTTTAACGAAAACAAAACTAAGAAAAAAGAGCAAAATTTGATAAACTACTGGGCATGTGCCCTGCCACTGATCATATTTTTCTCTATATGATGTTGTATATTATACTACTTCATAATTTTGAAAATTAATCAAAATAAAGCAGACTGCAGAACTATAAGTATACTATAATTTCA... | CATAAGGATACCTACATTACACTTTTTCTGTAAAGTTCTAAACTTTCGTCTCTGACTCATTAGAGTGTTTACCTTTTGAGAGAGGAAAAAGAGTTGGATCAGGGATGGTCCACAGGGACTCATCAAGTATAACTGTAGTGTGTTCTTTTTAACGAAAACAAAACTAAGAAAAAAGAGCAAAATTTGATAAACTACTGGGCATGTGCCCTGCCACTGATCATATTTTTCTCTATATGATGTTGTATATTATACTACTTCATAATTTTGAAAATTAATCAAAATAAAGCAGACTGCAGAACTATAAGTATACTATAATTTCA... |
Task1_train_34762 | A mutation on Chromosome 2 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | AGTCCCATGCCTTGGCATCAGCAGGGAAGCCCCAGGACAGTAGGCCAGAGGTGTGCCGCATGGGTGTAAGGCAACATGCTATGAGGTAAAGGGGTCAGAGATGACAGAGATGTGGCCCAATGGACTTGAAGTGGTGCTCAGAGGTCCTGACACAGGGAGCCTTTCCTTCGCATCCCTCTAGAGAGCCACTTAGCATTCTGTGTTGGCTCATAGGTACAATAGGTCCTCACAAACATATAGATCACACTTTATATTTTAACATACCTTTTCTGGGGCCAGGTGTGGTGGTGTGCCTATAATCCCAGCTTCTTCCAAGTCTC... | AGTCCCATGCCTTGGCATCAGCAGGGAAGCCCCAGGACAGTAGGCCAGAGGTGTGCCGCATGGGTGTAAGGCAACATGCTATGAGGTAAAGGGGTCAGAGATGACAGAGATGTGGCCCAATGGACTTGAAGTGGTGCTCAGAGGTCCTGACACAGGGAGCCTTTCCTTCGCATCCCTCTAGAGAGCCACTTAGCATTCTGTGTTGGCTCATAGGTACAATAGGTCCTCACAAACATATAGATCACACTTTATATTTTAACATACCTTTTCTGGGGCCAGGTGTGGTGGTGTGCCTATAATCCCAGCTTCTTCCAAGTCTC... |
Task1_train_34763 | A mutation on Chromosome 2 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GAGTCTCCTCTTTGGCTCAAGGGGAGCAGGTGAGCAGCTCACTGATGCTGACCACTTATTGCATTGTTGCATTTTCCATAGTTTCTCTACATTTGGCCTATCCAGGTGCAGCTCAAAGAAGATATGTAAGCAGTAAAATGGTTTGGATCACTATAAAAAGATACACCCCAGCTCAAGATCTTGCAAAAAATAGAATCTGAATAAATATGTGTTGATTAACTGACCAGAGACCCACCCAGAAGGTCATTTAAAGGGATCATCTTGATAGAGATATTTAAATACCTATGGGAAGTATAAAATTGTACAATAAAATGCAATTT... | GAGTCTCCTCTTTGGCTCAAGGGGAGCAGGTGAGCAGCTCACTGATGCTGACCACTTATTGCATTGTTGCATTTTCCATAGTTTCTCTACATTTGGCCTATCCAGGTGCAGCTCAAAGAAGATATGTAAGCAGTAAAATGGTTTGGATCACTATAAAAAGATACACCCCAGCTCAAGATCTTGCAAAAAATAGAATCTGAATAAATATGTGTTGATTAACTGACCAGAGACCCACCCAGAAGGTCATTTAAAGGGATCATCTTGATAGAGATATTTAAATACCTATGGGAAGTATAAAATTGTACAATAAAATGCAATTT... |
Task1_train_34764 | A genomic variant on Chromosome 2 is under review. What is the biological outcome — benign or pathogenic? | Benign | AAGTCATCTAAGCACTTTCTTTTAAAAGCATAAATTACAGGCATTAAAAAGCTAAAGGATGTGAATAGACATAGGGCTAGATCGTCAATATTCATCAATTTTATTTTCATTGTAAGTCTTTACTATATAATAACTCCCCAAGCCCTCCCCTGAGCTATTAGCCTCCCTCTCCTTCTCCCTCTCCTTCTGCACATCTATCTTCCGTTTTCATGCCATTTACTGCTGCTAGAATAACACAGAGATGGGAGAGCAGAGGGAGACATTATTTGCAATTCATACAATATTTTTCATTCATGAATGTCAAAGCACAATTTCTTGAA... | AAGTCATCTAAGCACTTTCTTTTAAAAGCATAAATTACAGGCATTAAAAAGCTAAAGGATGTGAATAGACATAGGGCTAGATCGTCAATATTCATCAATTTTATTTTCATTGTAAGTCTTTACTATATAATAACTCCCCAAGCCCTCCCCTGAGCTATTAGCCTCCCTCTCCTTCTCCCTCTCCTTCTGCACATCTATCTTCCGTTTTCATGCCATTTACTGCTGCTAGAATAACACAGAGATGGGAGAGCAGAGGGAGACATTATTTGCAATTCATACAATATTTTTCATTCATGAATGTCAAAGCACAATTTCTTGAA... |
Task1_train_34765 | Assess the clinical impact of this variant found on Chromosome 2. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | AATGAATGGAATGCAGAGAAAGCACATTTCAAGGAGATACTGAGGTTCTAGCCACTTGGTTCTCGTTTATTATTATAAAACTTCAATTTATAATGGCCAAAGGCTATAATCTTTTTGAGGTAGCTTTTTTCAGTGTTAGTTCTGAATATGAGCTTTTGCTATGCTTGAGATACACGCAAGTATTAGAAGAGCATCTCATCTGGAATGATGCACAAAAATTGATTATAAAGGTTGCCTGTGGGAACCTGGGTGGTTAAGGATAGGATTGAAAGTGGGACACTTCCTTTTCTCTGTATAGCTTGCGTACTTTGTACCGAGTA... | AATGAATGGAATGCAGAGAAAGCACATTTCAAGGAGATACTGAGGTTCTAGCCACTTGGTTCTCGTTTATTATTATAAAACTTCAATTTATAATGGCCAAAGGCTATAATCTTTTTGAGGTAGCTTTTTTCAGTGTTAGTTCTGAATATGAGCTTTTGCTATGCTTGAGATACACGCAAGTATTAGAAGAGCATCTCATCTGGAATGATGCACAAAAATTGATTATAAAGGTTGCCTGTGGGAACCTGGGTGGTTAAGGATAGGATTGAAAGTGGGACACTTCCTTTTCTCTGTATAGCTTGCGTACTTTGTACCGAGTA... |
Task1_train_34766 | Consider this mutation on Chromosome 2. Is this a benign change or a disease-causing variant? | Benign | ATGAATGGAATGCAGAGAAAGCACATTTCAAGGAGATACTGAGGTTCTAGCCACTTGGTTCTCGTTTATTATTATAAAACTTCAATTTATAATGGCCAAAGGCTATAATCTTTTTGAGGTAGCTTTTTTCAGTGTTAGTTCTGAATATGAGCTTTTGCTATGCTTGAGATACACGCAAGTATTAGAAGAGCATCTCATCTGGAATGATGCACAAAAATTGATTATAAAGGTTGCCTGTGGGAACCTGGGTGGTTAAGGATAGGATTGAAAGTGGGACACTTCCTTTTCTCTGTATAGCTTGCGTACTTTGTACCGAGTAC... | ATGAATGGAATGCAGAGAAAGCACATTTCAAGGAGATACTGAGGTTCTAGCCACTTGGTTCTCGTTTATTATTATAAAACTTCAATTTATAATGGCCAAAGGCTATAATCTTTTTGAGGTAGCTTTTTTCAGTGTTAGTTCTGAATATGAGCTTTTGCTATGCTTGAGATACACGCAAGTATTAGAAGAGCATCTCATCTGGAATGATGCACAAAAATTGATTATAAAGGTTGCCTGTGGGAACCTGGGTGGTTAAGGATAGGATTGAAAGTGGGACACTTCCTTTTCTCTGTATAGCTTGCGTACTTTGTACCGAGTAC... |
Task1_train_34767 | Assess the clinical impact of this variant found on Chromosome 2. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CAAAACTTTTATTACTTATATAGCCCATCATTTAACAAGCATCTCTATGGTACATCTTCTCTTAGGTTGAACGGTATGAAACTGCTGTTTTGGGATGTCAGAAATAGTTGAATGTCAACAGTTTTTCGTGGTTCAACCTATTTATTTTATTTATTCAGATACTCTTCTACTTGCTAGATATAAAAACTAAGGAGCCTCCCCTACCCCCCGCCACCCCCATTAAATGAGCTCAGTTCTTAGTGCAGAACTACAGCGTGGCGTCCGTTCTTCAACCAGATGTACAGTTTTTACTGATTAAATATGTCTGATTAAAGTGATGT... | CAAAACTTTTATTACTTATATAGCCCATCATTTAACAAGCATCTCTATGGTACATCTTCTCTTAGGTTGAACGGTATGAAACTGCTGTTTTGGGATGTCAGAAATAGTTGAATGTCAACAGTTTTTCGTGGTTCAACCTATTTATTTTATTTATTCAGATACTCTTCTACTTGCTAGATATAAAAACTAAGGAGCCTCCCCTACCCCCCGCCACCCCCATTAAATGAGCTCAGTTCTTAGTGCAGAACTACAGCGTGGCGTCCGTTCTTCAACCAGATGTACAGTTTTTACTGATTAAATATGTCTGATTAAAGTGATGT... |
Task1_train_34768 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GGATTTGTGGCAGAGCCAATTTATATCTAAAGCTGCATGTGTTATTCTAAGTGGATTGTCTTAACTCAGGAACTTCTAGGAGCTTCATGGAAATTGCTATCGTTAAGTCATGCTCAGCCAGCTGCTCCTGGCTTCTGGTGTAAGCAAATGCAAAAGAGGCTTCTACTACTCAAGCAGAGAGAAGCCTTCTACAGGGAAGAAAACAGACACACGGATGTACAGTTGCTTCATGCTGTTGAGTTGCAATGTGTTTTCTGTCTCTCAGCCTGGAAGAGAGCATTCATGGCAGTGTGAAGAAATAGCCCAAAACTTTCCAAAAG... | GGATTTGTGGCAGAGCCAATTTATATCTAAAGCTGCATGTGTTATTCTAAGTGGATTGTCTTAACTCAGGAACTTCTAGGAGCTTCATGGAAATTGCTATCGTTAAGTCATGCTCAGCCAGCTGCTCCTGGCTTCTGGTGTAAGCAAATGCAAAAGAGGCTTCTACTACTCAAGCAGAGAGAAGCCTTCTACAGGGAAGAAAACAGACACACGGATGTACAGTTGCTTCATGCTGTTGAGTTGCAATGTGTTTTCTGTCTCTCAGCCTGGAAGAGAGCATTCATGGCAGTGTGAAGAAATAGCCCAAAACTTTCCAAAAG... |
Task1_train_34769 | A genomic variant on Chromosome 2 is under review. What is the biological outcome — benign or pathogenic? | Benign | TGAGGTCATAGTTAATAATAGGGACTATTTTAAAGTAGTTTGTTTCCTCAAGGACCAAAATCTTTCCAAGTCTCTGCTCTGGCAGTCTTCAAAGTGTGATCTAAGGACCTCTGGAGGCCCTGAGCTTATTAAGATACTCCTCCTTTTTCCAACTGCATATCTGTGTCAGGCTGGATTTTTACTCCAGCCAAAACACTGTAGGATAATAGATTCATCAAAGAAGGAGAATGAGAATCCAGCTGTCTTTGATCAAGACAGACATTAAAGAGATTGGCAAAAATATAAAATAATGGCCACTGTACTCATTAATTCTTTTTTAT... | TGAGGTCATAGTTAATAATAGGGACTATTTTAAAGTAGTTTGTTTCCTCAAGGACCAAAATCTTTCCAAGTCTCTGCTCTGGCAGTCTTCAAAGTGTGATCTAAGGACCTCTGGAGGCCCTGAGCTTATTAAGATACTCCTCCTTTTTCCAACTGCATATCTGTGTCAGGCTGGATTTTTACTCCAGCCAAAACACTGTAGGATAATAGATTCATCAAAGAAGGAGAATGAGAATCCAGCTGTCTTTGATCAAGACAGACATTAAAGAGATTGGCAAAAATATAAAATAATGGCCACTGTACTCATTAATTCTTTTTTAT... |
Task1_train_34770 | This sequence variant lies on Chromosome 2. Is it clinically significant, and what condition might it cause if any? | Benign | TCCTCAAGGACCAAAATCTTTCCAAGTCTCTGCTCTGGCAGTCTTCAAAGTGTGATCTAAGGACCTCTGGAGGCCCTGAGCTTATTAAGATACTCCTCCTTTTTCCAACTGCATATCTGTGTCAGGCTGGATTTTTACTCCAGCCAAAACACTGTAGGATAATAGATTCATCAAAGAAGGAGAATGAGAATCCAGCTGTCTTTGATCAAGACAGACATTAAAGAGATTGGCAAAAATATAAAATAATGGCCACTGTACTCATTAATTCTTTTTTATTTTGGAAAATGGAGTTTTTTTTCCAAAATGTATTATGTATGTGA... | TCCTCAAGGACCAAAATCTTTCCAAGTCTCTGCTCTGGCAGTCTTCAAAGTGTGATCTAAGGACCTCTGGAGGCCCTGAGCTTATTAAGATACTCCTCCTTTTTCCAACTGCATATCTGTGTCAGGCTGGATTTTTACTCCAGCCAAAACACTGTAGGATAATAGATTCATCAAAGAAGGAGAATGAGAATCCAGCTGTCTTTGATCAAGACAGACATTAAAGAGATTGGCAAAAATATAAAATAATGGCCACTGTACTCATTAATTCTTTTTTATTTTGGAAAATGGAGTTTTTTTTCCAAAATGTATTATGTATGTGA... |
Task1_train_34771 | A variant was discovered on Chromosome 2. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | AATTTCCTAATAAAATAAAAATATATTATTAAAAGTTTATCTTTGCATTTTTTTTTTGGTTTGAACATATCTCACATTCTAGAAAATCTTAATCTCTCTTAGAAAGCCTTTGGTGGATGCGCAGTGATCGTGGAGCAAGTTAAAGACCCTGAGAGTAGCTTCCTGCCTCTGTTGTTTGTGCCCTCTAGTTACCAAACAGAATACTTGAATGTCCAGCTTCTCTCTACAGTTCGTATTCAATTTTGAGATGTGAGGTTCCTTTAAAAATAGACAAGCTGGGCCAGGCGCAGTGGCTCACATCTGTAATCCTAGCACTTTGG... | AATTTCCTAATAAAATAAAAATATATTATTAAAAGTTTATCTTTGCATTTTTTTTTTGGTTTGAACATATCTCACATTCTAGAAAATCTTAATCTCTCTTAGAAAGCCTTTGGTGGATGCGCAGTGATCGTGGAGCAAGTTAAAGACCCTGAGAGTAGCTTCCTGCCTCTGTTGTTTGTGCCCTCTAGTTACCAAACAGAATACTTGAATGTCCAGCTTCTCTCTACAGTTCGTATTCAATTTTGAGATGTGAGGTTCCTTTAAAAATAGACAAGCTGGGCCAGGCGCAGTGGCTCACATCTGTAATCCTAGCACTTTGG... |
Task1_train_34772 | This is a variant located on Chromosome 2. Is this mutation a likely cause of disease or not? | Benign | CCTTGAGGGTACAGACAAAGTCTTGTCCATCTTCAGAAACTGATTAAAGATCTAGCACTTTTTCTTGAAATTTCCCTGTAATCTGAATCAAGGCTTATGCTTTAGGACCATAGTGGGAGAAACCAGGGAGACAGTATATTAGCTTGCACTGCTGTAACAAAATACAACAGATTGGGTGGCTTAAACACCAAAAGAAATAGATTTTCTTAAAGTTCTGGAAACTGGAAGTCTAAGATCAAGATACCATCAGGATTCGGTTCTGGTGAGACTTCTCTTCCAGTCTTGTAGACAGCTGCCTTCTTACTGTGTCTTCACCTGAT... | CCTTGAGGGTACAGACAAAGTCTTGTCCATCTTCAGAAACTGATTAAAGATCTAGCACTTTTTCTTGAAATTTCCCTGTAATCTGAATCAAGGCTTATGCTTTAGGACCATAGTGGGAGAAACCAGGGAGACAGTATATTAGCTTGCACTGCTGTAACAAAATACAACAGATTGGGTGGCTTAAACACCAAAAGAAATAGATTTTCTTAAAGTTCTGGAAACTGGAAGTCTAAGATCAAGATACCATCAGGATTCGGTTCTGGTGAGACTTCTCTTCCAGTCTTGTAGACAGCTGCCTTCTTACTGTGTCTTCACCTGAT... |
Task1_train_34773 | Consider this mutation on Chromosome 2. Is this a benign change or a disease-causing variant? | Benign | GAGGGTACAGACAAAGTCTTGTCCATCTTCAGAAACTGATTAAAGATCTAGCACTTTTTCTTGAAATTTCCCTGTAATCTGAATCAAGGCTTATGCTTTAGGACCATAGTGGGAGAAACCAGGGAGACAGTATATTAGCTTGCACTGCTGTAACAAAATACAACAGATTGGGTGGCTTAAACACCAAAAGAAATAGATTTTCTTAAAGTTCTGGAAACTGGAAGTCTAAGATCAAGATACCATCAGGATTCGGTTCTGGTGAGACTTCTCTTCCAGTCTTGTAGACAGCTGCCTTCTTACTGTGTCTTCACCTGATCTTT... | GAGGGTACAGACAAAGTCTTGTCCATCTTCAGAAACTGATTAAAGATCTAGCACTTTTTCTTGAAATTTCCCTGTAATCTGAATCAAGGCTTATGCTTTAGGACCATAGTGGGAGAAACCAGGGAGACAGTATATTAGCTTGCACTGCTGTAACAAAATACAACAGATTGGGTGGCTTAAACACCAAAAGAAATAGATTTTCTTAAAGTTCTGGAAACTGGAAGTCTAAGATCAAGATACCATCAGGATTCGGTTCTGGTGAGACTTCTCTTCCAGTCTTGTAGACAGCTGCCTTCTTACTGTGTCTTCACCTGATCTTT... |
Task1_train_34774 | A mutation is present on Chromosome 2. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | AAAAGGTGCTCAACATCATTGATAAGAGAATTATAAATCAAAACTACAATGAGATATTATCTCACTTCAATTTGAATGGCTTTTATCCAAAAAACAAGCAATAAATGCTGATGAGAATGTGCAACCTCTGCCTCCCAGGTTCAAGGGATTCTCCTGCCTCAGCCTCCCCAGTAGCAGGGATTACAGGTTCTCACCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGATACGGGGTTTAATCATATTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCACCTGCTTTGGCCTCCCAAAGTGCTGGGATTACA... | AAAAGGTGCTCAACATCATTGATAAGAGAATTATAAATCAAAACTACAATGAGATATTATCTCACTTCAATTTGAATGGCTTTTATCCAAAAAACAAGCAATAAATGCTGATGAGAATGTGCAACCTCTGCCTCCCAGGTTCAAGGGATTCTCCTGCCTCAGCCTCCCCAGTAGCAGGGATTACAGGTTCTCACCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGATACGGGGTTTAATCATATTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCACCTGCTTTGGCCTCCCAAAGTGCTGGGATTACA... |
Task1_train_34775 | A variant found on Chromosome 2 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | TCTTTCCTCTTACCCTCTGTTTGAGACAGCCTGGCTATATCCTCAAAATTCCCATTCTAAACTGAGCATGGTGCCCAGCACTTTGGGAGGCTGAGGCAGGAGGGTCACTTGAGGCCAGGAGATCAAGGTGTCGGTGAGCTGTGATCACACCACTGCACTCCAGTCTGGGTGAGAGTGAGATCTTGTCTCAAAAATAAAAATAAAAATCCAATTTCAGTTTATTTTAAAACAGTGCTTTTCATATTGTGGTGTCAAGGAAATTTAGTATGGGGTTGCAAACAGCATTATTATTATTATTATTTGAGATGGAGTCTCACTGT... | TCTTTCCTCTTACCCTCTGTTTGAGACAGCCTGGCTATATCCTCAAAATTCCCATTCTAAACTGAGCATGGTGCCCAGCACTTTGGGAGGCTGAGGCAGGAGGGTCACTTGAGGCCAGGAGATCAAGGTGTCGGTGAGCTGTGATCACACCACTGCACTCCAGTCTGGGTGAGAGTGAGATCTTGTCTCAAAAATAAAAATAAAAATCCAATTTCAGTTTATTTTAAAACAGTGCTTTTCATATTGTGGTGTCAAGGAAATTTAGTATGGGGTTGCAAACAGCATTATTATTATTATTATTTGAGATGGAGTCTCACTGT... |
Task1_train_34776 | Here is a mutation located on Chromosome 2. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AGCCAAGGACTCTGTGTCATAAATAAGTTTAAGGAAAAGTGCTGTGCCTCGATGTGCACGTAGGCCAGAATTATGTTTGACTTTACACAAACATCTCAGTGCAGTAAAGAGCAGTATTGCCAACAGCATGTCTCATCTCCAGCCATAAGGTGTTTTCTCTTATGTCAGTAAATAGAATGTACAATCGGGTTTTACACCGAGACATTCCATTCCCAGGGATGAGCAGGAGACAGATGCCTTCCTCATATCTCAACTGCACAGAGGCCTTCCTCTTTCACTAATTCTCCTTAGCACAGACCCTTTATGGATGTCGGGCTGGG... | AGCCAAGGACTCTGTGTCATAAATAAGTTTAAGGAAAAGTGCTGTGCCTCGATGTGCACGTAGGCCAGAATTATGTTTGACTTTACACAAACATCTCAGTGCAGTAAAGAGCAGTATTGCCAACAGCATGTCTCATCTCCAGCCATAAGGTGTTTTCTCTTATGTCAGTAAATAGAATGTACAATCGGGTTTTACACCGAGACATTCCATTCCCAGGGATGAGCAGGAGACAGATGCCTTCCTCATATCTCAACTGCACAGAGGCCTTCCTCTTTCACTAATTCTCCTTAGCACAGACCCTTTATGGATGTCGGGCTGGG... |
Task1_train_34777 | This variant is found on Chromosome 2. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CATATGTCCTAGGAATTGTCTCCAAAAAATTAAAAGAAAAGAAGAACTTCATGTAAAGTCCTTTTGCAGCCTTCAAAGGCTATTCCTAAACTGGCATCCTTTTCCACAGTGCTATGATGTGGGGATTTCTACAGAAATCCCTTAGATTTCTGTAGAGCAGTGGATCTCAATGAGGGGCAATTTTGCCCCCAGGAGACACTTAGCAACATCCGAAGACATTTTTGCTTGTTTTTTTGTTTTGTTTTGTTTTGTTTTTGAGACAGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCACTATCTTGGCTCACTGCAAG... | CATATGTCCTAGGAATTGTCTCCAAAAAATTAAAAGAAAAGAAGAACTTCATGTAAAGTCCTTTTGCAGCCTTCAAAGGCTATTCCTAAACTGGCATCCTTTTCCACAGTGCTATGATGTGGGGATTTCTACAGAAATCCCTTAGATTTCTGTAGAGCAGTGGATCTCAATGAGGGGCAATTTTGCCCCCAGGAGACACTTAGCAACATCCGAAGACATTTTTGCTTGTTTTTTTGTTTTGTTTTGTTTTGTTTTTGAGACAGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCACTATCTTGGCTCACTGCAAG... |
Task1_train_34778 | This variant lies on Chromosome 2. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TGTAGAGCAGTGGATCTCAATGAGGGGCAATTTTGCCCCCAGGAGACACTTAGCAACATCCGAAGACATTTTTGCTTGTTTTTTTGTTTTGTTTTGTTTTGTTTTTGAGACAGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCACTATCTTGGCTCACTGCAAGCTCTGTCTCCCGGGGTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCGCCACCATGCCTGGCTAATTTTTTGTATTTTCAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATAGTCTCGATCCCCTGAC... | TGTAGAGCAGTGGATCTCAATGAGGGGCAATTTTGCCCCCAGGAGACACTTAGCAACATCCGAAGACATTTTTGCTTGTTTTTTTGTTTTGTTTTGTTTTGTTTTTGAGACAGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCACTATCTTGGCTCACTGCAAGCTCTGTCTCCCGGGGTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCGCCACCATGCCTGGCTAATTTTTTGTATTTTCAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATAGTCTCGATCCCCTGAC... |
Task1_train_34779 | A variant found on Chromosome 2 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | TGTGGGCATCATAGACATTATACGAGTGTCTCATGTAGGGCACTGGGCAGACAAAACAGAGAGCAGGAGGACTCCTCATAGCCCCACACCTGTGAGAGGTAGATCAAGGGAGGGTGTCTTAAGCCTTTCTTCTGCTTTCAAAAAGTCAGCTTATGAAAGAGGTGCCAGTTGTAAAACCACGGACACCGACATCCTGGGGGACATGCAGCCCCCTGCAGAGCCTGGTGGTTGTTGATCAGAACCTGCAGCGTAAGTTCCAAGAGGGACTGCGGGGTCTCCACCGCATGGGCCTCTTCTGTGCGTTGTCTGGAGAATAGAGA... | TGTGGGCATCATAGACATTATACGAGTGTCTCATGTAGGGCACTGGGCAGACAAAACAGAGAGCAGGAGGACTCCTCATAGCCCCACACCTGTGAGAGGTAGATCAAGGGAGGGTGTCTTAAGCCTTTCTTCTGCTTTCAAAAAGTCAGCTTATGAAAGAGGTGCCAGTTGTAAAACCACGGACACCGACATCCTGGGGGACATGCAGCCCCCTGCAGAGCCTGGTGGTTGTTGATCAGAACCTGCAGCGTAAGTTCCAAGAGGGACTGCGGGGTCTCCACCGCATGGGCCTCTTCTGTGCGTTGTCTGGAGAATAGAGA... |
Task1_train_34780 | This alteration on Chromosome 2 may affect genome function. Does it lead to a disease or is it benign? | Benign | TTGTGTGATGAAATATGTCAACAGTTACAATATATGCATAACTTAGTAGATCAGTATTTTTCAAATGTCCAGTGCATGATTATGCATGGACCATGCATGAATAAAAGATCCATCAAAAGTGTGAAATAGACCAATGAGGTTTAATGCAAGTATATGGAAAATTCACTAATATGGTTTCAGATTCTATATTGCAACTAATTTTAAGAAGTTACCATTTGTTGAGTTTTAATATCAAAAAATGTTCACAATGATATAAAAAGGCAATTATAATACTCCTTCATTTTTCAACTATGTATCAGTGTCTGACTACATTCTTTTCT... | TTGTGTGATGAAATATGTCAACAGTTACAATATATGCATAACTTAGTAGATCAGTATTTTTCAAATGTCCAGTGCATGATTATGCATGGACCATGCATGAATAAAAGATCCATCAAAAGTGTGAAATAGACCAATGAGGTTTAATGCAAGTATATGGAAAATTCACTAATATGGTTTCAGATTCTATATTGCAACTAATTTTAAGAAGTTACCATTTGTTGAGTTTTAATATCAAAAAATGTTCACAATGATATAAAAAGGCAATTATAATACTCCTTCATTTTTCAACTATGTATCAGTGTCTGACTACATTCTTTTCT... |
Task1_train_34781 | Consider this mutation on Chromosome 2. Is this a benign change or a disease-causing variant? | Benign | ACATAAAATAAGCAGTTTGCTAAGGCTTCCATAATAAGGTAGCACAAACTGAGTGGCTTACACAACCAAAATGTATTGTGTCACAGTTGGGGAGGTTAGAGGTCAGAGGTCAAGGTGTCATCAGGGTCAGTTCCTTCTGAGGCCTTGGGAAAGAAGCTGTTCCACAGCTCCTGTAGCTTCTGGTGGTTTGCTGGCAATCTTTGGTGTGGAGAAGCATCACCCTGAGCTCTGCCCTCATCTTCACATGGTTTTCCCTGTGCATGTCTGTGCCTATATGGCCTGTTCTTATAAGGATGTATTGAACTAGGGCCCACCCTACT... | ACATAAAATAAGCAGTTTGCTAAGGCTTCCATAATAAGGTAGCACAAACTGAGTGGCTTACACAACCAAAATGTATTGTGTCACAGTTGGGGAGGTTAGAGGTCAGAGGTCAAGGTGTCATCAGGGTCAGTTCCTTCTGAGGCCTTGGGAAAGAAGCTGTTCCACAGCTCCTGTAGCTTCTGGTGGTTTGCTGGCAATCTTTGGTGTGGAGAAGCATCACCCTGAGCTCTGCCCTCATCTTCACATGGTTTTCCCTGTGCATGTCTGTGCCTATATGGCCTGTTCTTATAAGGATGTATTGAACTAGGGCCCACCCTACT... |
Task1_train_34782 | Mutation context: Chromosome 2. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GCTTGAGGCCAGGAGTTTGAGATGAGCCTGGGCAACATAGTGAGACCCCATCTCTACAAAATTAAACAAAAATTAGCTAATTAAAACAAAAATTAGTCAGGTGTGGTGGCATGCACCTGTAGACCTAACTACTCAGTAAGCTGAGGAAAATAACCTGAGCCCAGGAGGAGTTCAAGGTTACAGCGAACTATGATTATGCCACTATAATCCAGTCTGAGTGACAGAGTGAGACCCCATCTTCTTGATGAATATATTTGTGGATGAACACACACACACACACACACACACACACACCCCTCATATTCTAGACAGCCATATGT... | GCTTGAGGCCAGGAGTTTGAGATGAGCCTGGGCAACATAGTGAGACCCCATCTCTACAAAATTAAACAAAAATTAGCTAATTAAAACAAAAATTAGTCAGGTGTGGTGGCATGCACCTGTAGACCTAACTACTCAGTAAGCTGAGGAAAATAACCTGAGCCCAGGAGGAGTTCAAGGTTACAGCGAACTATGATTATGCCACTATAATCCAGTCTGAGTGACAGAGTGAGACCCCATCTTCTTGATGAATATATTTGTGGATGAACACACACACACACACACACACACACACACCCCTCATATTCTAGACAGCCATATGT... |
Task1_train_34783 | Mutation context: Chromosome 2. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | AGGGACAAGAAGGTAAAGAACATTTCATTTCAGGCTGCTAGATTTTGGCACTGAGAATTAAAATGCAATTACACAGTTAAAAAAATCCAGATTGTAAGCCCAAGGTCATTTAACTTGAGAAAGATCCTTTTAAAATAAAGAACTACTGGGAAGTATTTTATGGAGAAAACAGGGCACAGGGGCTTGGCCTGGGAAATCGCTCATGTACCCGATTTGCTCCTAGTCAAAAAGGGACAATAATATCTGTTCTGTTTTTTCACAGGCTTGTTGAGAAGCAAGTAGGATGAGGCACATGGAGGCACTTTGTGACAATAAGACAT... | AGGGACAAGAAGGTAAAGAACATTTCATTTCAGGCTGCTAGATTTTGGCACTGAGAATTAAAATGCAATTACACAGTTAAAAAAATCCAGATTGTAAGCCCAAGGTCATTTAACTTGAGAAAGATCCTTTTAAAATAAAGAACTACTGGGAAGTATTTTATGGAGAAAACAGGGCACAGGGGCTTGGCCTGGGAAATCGCTCATGTACCCGATTTGCTCCTAGTCAAAAAGGGACAATAATATCTGTTCTGTTTTTTCACAGGCTTGTTGAGAAGCAAGTAGGATGAGGCACATGGAGGCACTTTGTGACAATAAGACAT... |
Task1_train_34784 | This variant is present on Chromosome 2. Is the change likely to result in a pathogenic outcome? | Benign | ACTCATTTTTTTTTTTTTTGGTCTTGAAAATTTAGTTCTTGCACCAATCAAATCCTTTATGTCTAAAATTTAGACTAAACACTGATTAAGACGCAAACTCCAGTCACATGCACCCTATGTAGTCTGAGACGATTCACTCACCTATGGATTTGACAAGCGCTCACGGCTGTGTCTCCACCTCTCACCACATCTGGGATGTTTTTGTCATTCGAATGCCCTTCTGCTTCCTCTAGGAGGCTGCTTTTGGAAAGGAAGGGTTCAGGTTCCCCAGCACAGGCTTCTCTCTGATCTGTTTCAATCTGAATCAAAGGCACTTCCCT... | ACTCATTTTTTTTTTTTTTGGTCTTGAAAATTTAGTTCTTGCACCAATCAAATCCTTTATGTCTAAAATTTAGACTAAACACTGATTAAGACGCAAACTCCAGTCACATGCACCCTATGTAGTCTGAGACGATTCACTCACCTATGGATTTGACAAGCGCTCACGGCTGTGTCTCCACCTCTCACCACATCTGGGATGTTTTTGTCATTCGAATGCCCTTCTGCTTCCTCTAGGAGGCTGCTTTTGGAAAGGAAGGGTTCAGGTTCCCCAGCACAGGCTTCTCTCTGATCTGTTTCAATCTGAATCAAAGGCACTTCCCT... |
Task1_train_34785 | An alteration has been detected on Chromosome 2. Is it pathogenic, and if so, what disease is involved? | Benign | GTCAGTCCCACCTCTCCGATACAAGCAAGAGTCAGATTTGCAGAGACCGGATGAGGACGCGCTACTGACCGGCTGCACGCTTAGGAAATCTTGTGGGCAGTTCTGAGCAAAGCCATCTAAAGAGTTGGCTTTGATGGGCACATTCACTGTCAGCCTGGAGCATGGGGATCTGCTGTCTGGCATGGACGACTGTCTGTGGCACACTGGGGATCGCAGAGAAGGAGACAGCAGGCCGGCTGTCCAATCCTGGCTGCTCCGTCTGGAGGAGGCACTTTCTCTGCTGTCTCTTTCGATGTCCCTCAGCATGTACCTGTAGAACT... | GTCAGTCCCACCTCTCCGATACAAGCAAGAGTCAGATTTGCAGAGACCGGATGAGGACGCGCTACTGACCGGCTGCACGCTTAGGAAATCTTGTGGGCAGTTCTGAGCAAAGCCATCTAAAGAGTTGGCTTTGATGGGCACATTCACTGTCAGCCTGGAGCATGGGGATCTGCTGTCTGGCATGGACGACTGTCTGTGGCACACTGGGGATCGCAGAGAAGGAGACAGCAGGCCGGCTGTCCAATCCTGGCTGCTCCGTCTGGAGGAGGCACTTTCTCTGCTGTCTCTTTCGATGTCCCTCAGCATGTACCTGTAGAACT... |
Task1_train_34786 | A variant was discovered on Chromosome 2. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CCAGTTTTGGGGCCCCTGTGATCTATATGCATACCCCACCATCACCCTGTTTTCCTCTCTCTTAAAAGGAGGTAGTCTTGGCCGGGCATGGTGGCTAATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGTGGATCACCAGGTCAGGAGTTCGAGACCAGCCTGACCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGGGCATGGTGGTGGGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGGGGCGGAGGTTGCAGTGAGCTGAGATCGTGCCA... | CCAGTTTTGGGGCCCCTGTGATCTATATGCATACCCCACCATCACCCTGTTTTCCTCTCTCTTAAAAGGAGGTAGTCTTGGCCGGGCATGGTGGCTAATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGTGGATCACCAGGTCAGGAGTTCGAGACCAGCCTGACCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGGGCATGGTGGTGGGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGGGGCGGAGGTTGCAGTGAGCTGAGATCGTGCCA... |
Task1_train_34787 | A mutation is present on Chromosome 2. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TCCTGGCCTCAGATGATTCCCTCACCTCGGACTCCCAAAAAGCTGGGATTACAGATGTGAGTCACCATGCCCAGCCTCACTCTTATTTTTTTAGGAGCCCAGCAGTAAGGCAGAATGGATGGGGAGATGCTGCTACTAAAATGTTGAAAAGCATGAGACTCCAGCTGGTTGTTAATTTCCACCTGACAGGCGATTTAGACTGAAGGGTTAGTTTTGATCATGGCAAATCTGAGCATGATGCAAAATAGCTTAACAATTTTTGTAAATGCATTTCTTGGAAGCCCACTCGCTGAGGAAGGATGACCCTCTGTTCTCCAGGA... | TCCTGGCCTCAGATGATTCCCTCACCTCGGACTCCCAAAAAGCTGGGATTACAGATGTGAGTCACCATGCCCAGCCTCACTCTTATTTTTTTAGGAGCCCAGCAGTAAGGCAGAATGGATGGGGAGATGCTGCTACTAAAATGTTGAAAAGCATGAGACTCCAGCTGGTTGTTAATTTCCACCTGACAGGCGATTTAGACTGAAGGGTTAGTTTTGATCATGGCAAATCTGAGCATGATGCAAAATAGCTTAACAATTTTTGTAAATGCATTTCTTGGAAGCCCACTCGCTGAGGAAGGATGACCCTCTGTTCTCCAGGA... |
Task1_train_34788 | Here’s a variant located on Chromosome 2. What is the predicted biological effect — harmless or disease-causing? | Benign | TGCAGGATAGCTCAACCAGCTGTCCCTCCCTAGTAAAGGAGGATGAAACCAACATTGGATCTGAAGGCAATTCCAGATGTTTGAGTCCAATGAGAAATTTATGTGTAAAAATATGCAAGCCTGATTATCCAGGAAGTTTAATTGATTTTATGTTGTTTACTTATTTATTTTCATATTTCTGAGGCAGGAAGAACAATGTAGGCATAAACTGCCTTTCCTTCCAGTTTGAACAAAGAGGCTGGATGCCATTTACTGCTCTCGTTGGGAGCGAGCTGCCGATCTGGGAACAGAGCATGGTTTTTTTCAGCTTCTGTTCCAGA... | TGCAGGATAGCTCAACCAGCTGTCCCTCCCTAGTAAAGGAGGATGAAACCAACATTGGATCTGAAGGCAATTCCAGATGTTTGAGTCCAATGAGAAATTTATGTGTAAAAATATGCAAGCCTGATTATCCAGGAAGTTTAATTGATTTTATGTTGTTTACTTATTTATTTTCATATTTCTGAGGCAGGAAGAACAATGTAGGCATAAACTGCCTTTCCTTCCAGTTTGAACAAAGAGGCTGGATGCCATTTACTGCTCTCGTTGGGAGCGAGCTGCCGATCTGGGAACAGAGCATGGTTTTTTTCAGCTTCTGTTCCAGA... |
Task1_train_34789 | This variant is present on Chromosome 2. Is the change likely to result in a pathogenic outcome? | Benign | CAGCATGGGAAAGATGATTTATATAATAGATGGCATTGGGAGACCAGTGCCTTAAACTTTGAATGAATCCAGCCTGGTCAGGCCAGCCTCCAGGGCAAGATGGGGGAGGCACCATTGTCTCTGCTGGAAGTTCACAACTAACGGGAAGCTCATGAGTGGAGCTGATGTGTCTGGAGAACACATCTAAGCAAGTAGAGGAGGTTGAGGAGGGGGAGTTAGTGCAGCCAATAGATGACTGCCATTTCCAGCTGTAGGGATGCCCTGTAGAGACAAAGCTCAGTTCAAAGGCGTCATTCCATCCTGGTGCTACCAATAAGAAG... | CAGCATGGGAAAGATGATTTATATAATAGATGGCATTGGGAGACCAGTGCCTTAAACTTTGAATGAATCCAGCCTGGTCAGGCCAGCCTCCAGGGCAAGATGGGGGAGGCACCATTGTCTCTGCTGGAAGTTCACAACTAACGGGAAGCTCATGAGTGGAGCTGATGTGTCTGGAGAACACATCTAAGCAAGTAGAGGAGGTTGAGGAGGGGGAGTTAGTGCAGCCAATAGATGACTGCCATTTCCAGCTGTAGGGATGCCCTGTAGAGACAAAGCTCAGTTCAAAGGCGTCATTCCATCCTGGTGCTACCAATAAGAAG... |
Task1_train_34790 | Consider this mutation on Chromosome 2. Is this a benign change or a disease-causing variant? | Benign | CAAGCCCTCCAGTGGATGCCTGAAACCATGGGTAGTGCCCACCCCTGCAGATACTATGTTTCTTCAATCTGATAACCAAGACAGCTACTAAGTGACTGATGGGTGGGCTGCGTATACAGCAGGACACACTGGACCAAGGGATGATTCGCATCCCCGAGTGGGATACAGCAGGATGGTGCAAGACTTTGTCACGCTACTCAGAACAGCGCATCATTTTTAACTTATAAATTGTTTATTTCTGGAACTTTCCATTTAATATTTTCAAACTGCAGTTGACTTCAGGTAACTGAAATCATGGATCAAAAAACTGCTTATAAAGG... | CAAGCCCTCCAGTGGATGCCTGAAACCATGGGTAGTGCCCACCCCTGCAGATACTATGTTTCTTCAATCTGATAACCAAGACAGCTACTAAGTGACTGATGGGTGGGCTGCGTATACAGCAGGACACACTGGACCAAGGGATGATTCGCATCCCCGAGTGGGATACAGCAGGATGGTGCAAGACTTTGTCACGCTACTCAGAACAGCGCATCATTTTTAACTTATAAATTGTTTATTTCTGGAACTTTCCATTTAATATTTTCAAACTGCAGTTGACTTCAGGTAACTGAAATCATGGATCAAAAAACTGCTTATAAAGG... |
Task1_train_34791 | A genetic alteration is present on Chromosome 2. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | AGAGAATACACATAACATGGTGAGAGGGCATTGACTAATAAGTAGAATGGGGGAGAAAGCAGCTTGTCTCTCCTTCCTGCCCAGGAAGGTCACTTACTTTTCTTAGAATGGAATCATTTCTGTTAAGTGTCTTAAAAGGACACCAGCCCTGTGATTTTGGACACTGGGATCATACTAATGATAAACTAAGTCAGGGAAGAGGAGCTTTAAGCCACTGGCTTAGGCTGCCATCTATTGCTCTGTTTCCTTTTACAGCTAGAGTTGTCTACATATGTTATCACCTCCCATTCATTATCCTTCCCACACAACTGGCTCCTGCC... | AGAGAATACACATAACATGGTGAGAGGGCATTGACTAATAAGTAGAATGGGGGAGAAAGCAGCTTGTCTCTCCTTCCTGCCCAGGAAGGTCACTTACTTTTCTTAGAATGGAATCATTTCTGTTAAGTGTCTTAAAAGGACACCAGCCCTGTGATTTTGGACACTGGGATCATACTAATGATAAACTAAGTCAGGGAAGAGGAGCTTTAAGCCACTGGCTTAGGCTGCCATCTATTGCTCTGTTTCCTTTTACAGCTAGAGTTGTCTACATATGTTATCACCTCCCATTCATTATCCTTCCCACACAACTGGCTCCTGCC... |
Task1_train_34792 | Assess the clinical impact of this variant found on Chromosome 2. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GTCACATGGTTTCTGCTCCCAGCAGCCCCTGCTCAAGGAATGAAGCTGAGAGCGGAAAGTGGTGATATTGAAATCTGATGTCCATGATGAAGGGGAATGTCTTTGCTGTATGAAAAATACATCTTATTGCTTTGACGTCTATGTGTGGATATTCTTTAACTGCTCTATCTGTGGTTATTTTACTTGGAGAAATAGTGGAGAAGGCTAAATGCCTTATATATTTCTGTATATAAGGATTGTTTGAAGAAAGCAGGAGCTAGCCTGTGCTTGCTAGCACCTGTTAACAGCAAAGACATATAAAGCTCTGCTAGTTTTTGCTG... | GTCACATGGTTTCTGCTCCCAGCAGCCCCTGCTCAAGGAATGAAGCTGAGAGCGGAAAGTGGTGATATTGAAATCTGATGTCCATGATGAAGGGGAATGTCTTTGCTGTATGAAAAATACATCTTATTGCTTTGACGTCTATGTGTGGATATTCTTTAACTGCTCTATCTGTGGTTATTTTACTTGGAGAAATAGTGGAGAAGGCTAAATGCCTTATATATTTCTGTATATAAGGATTGTTTGAAGAAAGCAGGAGCTAGCCTGTGCTTGCTAGCACCTGTTAACAGCAAAGACATATAAAGCTCTGCTAGTTTTTGCTG... |
Task1_train_34793 | A mutation on Chromosome 2 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CACATGGTTTCTGCTCCCAGCAGCCCCTGCTCAAGGAATGAAGCTGAGAGCGGAAAGTGGTGATATTGAAATCTGATGTCCATGATGAAGGGGAATGTCTTTGCTGTATGAAAAATACATCTTATTGCTTTGACGTCTATGTGTGGATATTCTTTAACTGCTCTATCTGTGGTTATTTTACTTGGAGAAATAGTGGAGAAGGCTAAATGCCTTATATATTTCTGTATATAAGGATTGTTTGAAGAAAGCAGGAGCTAGCCTGTGCTTGCTAGCACCTGTTAACAGCAAAGACATATAAAGCTCTGCTAGTTTTTGCTGCA... | CACATGGTTTCTGCTCCCAGCAGCCCCTGCTCAAGGAATGAAGCTGAGAGCGGAAAGTGGTGATATTGAAATCTGATGTCCATGATGAAGGGGAATGTCTTTGCTGTATGAAAAATACATCTTATTGCTTTGACGTCTATGTGTGGATATTCTTTAACTGCTCTATCTGTGGTTATTTTACTTGGAGAAATAGTGGAGAAGGCTAAATGCCTTATATATTTCTGTATATAAGGATTGTTTGAAGAAAGCAGGAGCTAGCCTGTGCTTGCTAGCACCTGTTAACAGCAAAGACATATAAAGCTCTGCTAGTTTTTGCTGCA... |
Task1_train_34794 | This variant is located on Chromosome 2. Evaluate its biological effect and specify any disease association. | Benign | AAATTCCCCACAGTCAGGTGGGGGCTTGGAAGGAGGACCATCCATGTCTGCTGCAGCAATTCACTATTAGGGCCACACAGTGTTTTTGTTCATTTGCTTTGCATTTTGACAGAGCCGTTTTGAGCACTACTTTATTGAAGTGGCCTCAGAAGAGTGGCTCTGTCAAACAGTCCAGCCTGACTCAGTTCCCTTGCTTTCCCCTGGGGTTCCTGCCACAACCCTTTGTGGCAGGTGAATGTTTCCCTTTCAGGCGCTTTGTGGCATTTGGAGTCCAAACCTACAGGCACTGGTGGGGCTCTGTCCATCATCATCCGTGGCCC... | AAATTCCCCACAGTCAGGTGGGGGCTTGGAAGGAGGACCATCCATGTCTGCTGCAGCAATTCACTATTAGGGCCACACAGTGTTTTTGTTCATTTGCTTTGCATTTTGACAGAGCCGTTTTGAGCACTACTTTATTGAAGTGGCCTCAGAAGAGTGGCTCTGTCAAACAGTCCAGCCTGACTCAGTTCCCTTGCTTTCCCCTGGGGTTCCTGCCACAACCCTTTGTGGCAGGTGAATGTTTCCCTTTCAGGCGCTTTGTGGCATTTGGAGTCCAAACCTACAGGCACTGGTGGGGCTCTGTCCATCATCATCCGTGGCCC... |
Task1_train_34795 | This mutation on Chromosome 2 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TGAAGTGATACTCTGAGGCACGTAGAAATGCCATGGAGAATGGCCTCCCAGCAAATTCACCCCACATTTTTGCTTCTGGCAAATTTCCCCATGAAGACACCACCCCATCAGCCACTCTGATTATTCGGACCCATGGGTCCACATCCATTCAATTTTTTTCCTGCAACATTTAACAAATCTTGACCCAGTGCAGCGGCTCACTCATGTTATCCCAGTACTTTGGGAGGCCAATACAGGAGGATCACTTGAGGTCAGGAGTTCAAAAACCAGCCTGGACAACATAGTGAGACCCCGTATCTACACACACACACGTACCCACA... | TGAAGTGATACTCTGAGGCACGTAGAAATGCCATGGAGAATGGCCTCCCAGCAAATTCACCCCACATTTTTGCTTCTGGCAAATTTCCCCATGAAGACACCACCCCATCAGCCACTCTGATTATTCGGACCCATGGGTCCACATCCATTCAATTTTTTTCCTGCAACATTTAACAAATCTTGACCCAGTGCAGCGGCTCACTCATGTTATCCCAGTACTTTGGGAGGCCAATACAGGAGGATCACTTGAGGTCAGGAGTTCAAAAACCAGCCTGGACAACATAGTGAGACCCCGTATCTACACACACACACGTACCCACA... |
Task1_train_34796 | Here is a genetic alteration on Chromosome 2. Based on the data, is it a benign variant or a cause of disease? | Benign | TCTGAGGCACGTAGAAATGCCATGGAGAATGGCCTCCCAGCAAATTCACCCCACATTTTTGCTTCTGGCAAATTTCCCCATGAAGACACCACCCCATCAGCCACTCTGATTATTCGGACCCATGGGTCCACATCCATTCAATTTTTTTCCTGCAACATTTAACAAATCTTGACCCAGTGCAGCGGCTCACTCATGTTATCCCAGTACTTTGGGAGGCCAATACAGGAGGATCACTTGAGGTCAGGAGTTCAAAAACCAGCCTGGACAACATAGTGAGACCCCGTATCTACACACACACACGTACCCACACACATTTCATA... | TCTGAGGCACGTAGAAATGCCATGGAGAATGGCCTCCCAGCAAATTCACCCCACATTTTTGCTTCTGGCAAATTTCCCCATGAAGACACCACCCCATCAGCCACTCTGATTATTCGGACCCATGGGTCCACATCCATTCAATTTTTTTCCTGCAACATTTAACAAATCTTGACCCAGTGCAGCGGCTCACTCATGTTATCCCAGTACTTTGGGAGGCCAATACAGGAGGATCACTTGAGGTCAGGAGTTCAAAAACCAGCCTGGACAACATAGTGAGACCCCGTATCTACACACACACACGTACCCACACACATTTCATA... |
Task1_train_34797 | A mutation located on Chromosome 2 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | AGAGCCGGCGGAGGACTTGTAGATAGACCATTCTAGGCCCTCCCAGTGTTACCAGATGTCCAGGCTGCACATAATATTGAACTCTAATTTTAGTCCTTACAGCACTTTTCACTTGAACGGCAAAGGGCTCAGTCACAGACTGGTTCTTTGTTGTAAATACACATGTATTTGTCTACAATACAGCATGTATGTATTGGTCTCTATATTTGCTCTATAAATTCTGTTGGTTTTTAATGACCGGGATTTGCTCCACAACACGTGGATGCAAATACCATCATATTTTAATTTCCCCAAATGAAATTAAATCTGGCTAAAGGTGT... | AGAGCCGGCGGAGGACTTGTAGATAGACCATTCTAGGCCCTCCCAGTGTTACCAGATGTCCAGGCTGCACATAATATTGAACTCTAATTTTAGTCCTTACAGCACTTTTCACTTGAACGGCAAAGGGCTCAGTCACAGACTGGTTCTTTGTTGTAAATACACATGTATTTGTCTACAATACAGCATGTATGTATTGGTCTCTATATTTGCTCTATAAATTCTGTTGGTTTTTAATGACCGGGATTTGCTCCACAACACGTGGATGCAAATACCATCATATTTTAATTTCCCCAAATGAAATTAAATCTGGCTAAAGGTGT... |
Task1_train_34798 | A mutation located on Chromosome 2 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | ATACATAAATCAGACAAAACACTTCTATCCATAATCTGTAAAAGGACTCCTACCTGTCAATAAATAAAATAAAATTCTATAATATAAATGGGTCAAACATTTGAACAGACACTTCACCAAAAAATAAATAAATTGCCAGTAAACACATGAAAACATGCTTGACATAATTTCCTGATTAAAGAAATACAAATTAAAACTAAAATTAGCTATCACATCGTACACACTGGAATGGCTAAAACTAGAAAGGCCATCACTGGTAGTCTTTGCAAAAACAGTTTGGCAGGTTTTAAAATGGTTAAATGTACTCTTACACAATGACC... | ATACATAAATCAGACAAAACACTTCTATCCATAATCTGTAAAAGGACTCCTACCTGTCAATAAATAAAATAAAATTCTATAATATAAATGGGTCAAACATTTGAACAGACACTTCACCAAAAAATAAATAAATTGCCAGTAAACACATGAAAACATGCTTGACATAATTTCCTGATTAAAGAAATACAAATTAAAACTAAAATTAGCTATCACATCGTACACACTGGAATGGCTAAAACTAGAAAGGCCATCACTGGTAGTCTTTGCAAAAACAGTTTGGCAGGTTTTAAAATGGTTAAATGTACTCTTACACAATGACC... |
Task1_train_34799 | Mutation context: Chromosome 2. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | ATCAGCCACTCTGATTAATTTGACCCATGGGTCCAGATATATTTGATTTGTTAAATGTTGTAGGAACAAATTGCAAATGTAGGTGCAGTGGCTCACTCATGTTATCTCAGCACTTTGGGAGACCAAGGCAGAAGGATCACTTGAGGCCAGGAGTCCAAAAACAAGCAAAACAACCAAAACAAGCCTGGGCAAGATAGTGGGACCCTGTCTCTCTACACACACACACACACACACACACACACACACACACACACACACACACATTTCATAAACCGTGAATGCTTTAGGTCTTTAGGTCCCTTATGACCAGCTGACCACCT... | ATCAGCCACTCTGATTAATTTGACCCATGGGTCCAGATATATTTGATTTGTTAAATGTTGTAGGAACAAATTGCAAATGTAGGTGCAGTGGCTCACTCATGTTATCTCAGCACTTTGGGAGACCAAGGCAGAAGGATCACTTGAGGCCAGGAGTCCAAAAACAAGCAAAACAACCAAAACAAGCCTGGGCAAGATAGTGGGACCCTGTCTCTCTACACACACACACACACACACACACACACACACACACACACACACACACATTTCATAAACCGTGAATGCTTTAGGTCTTTAGGTCCCTTATGACCAGCTGACCACCT... |
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