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_38900 | A mutation on Chromosome 7 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | AATACTGACTGCCTAAAACAATACGAATTTCTAACCTCTAGGATTAAAAATATTATATCAGCAATACATACAGTGCATCTTTTTCTTTTTTTTTTTTTTAATAGAGACAAGATCTAGCTCTGTCACCCAGACTGGAGTGTAGTGACACAATCATAGCTCACTGCAGCATCAAACTCCTGGGCTCAAATGGTGCTCCCTCTGCAGCTTCCTGAGTAGCTGGGACTACAGGCACGCGCCACCATGCTCAGCTAATTTTTTTAAAAATTTTTGTAGAGACAAGGTCTCTTTATGTTGCCCAGGCTAGTTGTGTATTCCCAGCC... | AATACTGACTGCCTAAAACAATACGAATTTCTAACCTCTAGGATTAAAAATATTATATCAGCAATACATACAGTGCATCTTTTTCTTTTTTTTTTTTTTAATAGAGACAAGATCTAGCTCTGTCACCCAGACTGGAGTGTAGTGACACAATCATAGCTCACTGCAGCATCAAACTCCTGGGCTCAAATGGTGCTCCCTCTGCAGCTTCCTGAGTAGCTGGGACTACAGGCACGCGCCACCATGCTCAGCTAATTTTTTTAAAAATTTTTGTAGAGACAAGGTCTCTTTATGTTGCCCAGGCTAGTTGTGTATTCCCAGCC... |
Task1_train_38901 | A genomic change on Chromosome 7 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | AAACAGAAACTTAGGGAGACAGGGAGGAATTTTCTTCAAAAGTTGAATAAAAATGTAAGCATCCACCTCACACAACAGTGAGTTTCTTCTGCCTGGAACTACTGAAGCAGAAGCTGGATGATTATCTTCCAAGAATGACAAAGAAAGATTCCAATCTGGGAGGTTAGGGTACGTGATCTCTCTAAGACCACTTCCATCTTTAAGATTTATGATTCTGGGCCGGGAGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAAGCCGAGGCAGGAGGATCACGAGGTCAAGAGATCAAGACCATCCTGGCCAACATGGTGA... | AAACAGAAACTTAGGGAGACAGGGAGGAATTTTCTTCAAAAGTTGAATAAAAATGTAAGCATCCACCTCACACAACAGTGAGTTTCTTCTGCCTGGAACTACTGAAGCAGAAGCTGGATGATTATCTTCCAAGAATGACAAAGAAAGATTCCAATCTGGGAGGTTAGGGTACGTGATCTCTCTAAGACCACTTCCATCTTTAAGATTTATGATTCTGGGCCGGGAGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAAGCCGAGGCAGGAGGATCACGAGGTCAAGAGATCAAGACCATCCTGGCCAACATGGTGA... |
Task1_train_38902 | Assess the clinical impact of this variant found on Chromosome 7. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GGAGTGCAGTGGCACAATCTTAGTTCACTGCAACCTCCGCCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGCGTGCCACCATACCCAGCTAATTTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATGTTGGCTGGGATGGTCTCAAATTCCTGACCTCAGGTGATCCACCCGCCTCGGCTTCCCACAGTGCAGGGATTGCAGGCGTGAGCCACTGTGCCTGGCTGATAATTTTTTTTTTTTTTTGACATGCCGTTTCGCTGTTGTCACCCAGGCTGGAGTGCAATAGTGCG... | GGAGTGCAGTGGCACAATCTTAGTTCACTGCAACCTCCGCCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGCGTGCCACCATACCCAGCTAATTTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATGTTGGCTGGGATGGTCTCAAATTCCTGACCTCAGGTGATCCACCCGCCTCGGCTTCCCACAGTGCAGGGATTGCAGGCGTGAGCCACTGTGCCTGGCTGATAATTTTTTTTTTTTTTTGACATGCCGTTTCGCTGTTGTCACCCAGGCTGGAGTGCAATAGTGCG... |
Task1_train_38903 | This variant is found on Chromosome 7. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GCTTTGCTGACAAGTAAACACAGGTGTGGTGTTTTTTTTTTGTTTGTTTGTTTTTGCGGTGGTACTTAACAATACTAGAAAATCAAACTATGAGGACTCAACTTCGGGAACTGAAAAATTACCCAATTTTCTCTACCCCAAACCTGGAGCTCAACTACATTAAAGACGGTTTTCCATACTGTTTGTTATTTCTGGTTTCTACATGAGGTTAAGACCCTAGTTAAAACCTGTCGGAAAATAAGGGTGACAGGCACGTAAACTCTCTTATGCCTTTAAAGAAAAACAACTTCATCGAGATTTTTCAACTACTCAGCTTGATA... | GCTTTGCTGACAAGTAAACACAGGTGTGGTGTTTTTTTTTTGTTTGTTTGTTTTTGCGGTGGTACTTAACAATACTAGAAAATCAAACTATGAGGACTCAACTTCGGGAACTGAAAAATTACCCAATTTTCTCTACCCCAAACCTGGAGCTCAACTACATTAAAGACGGTTTTCCATACTGTTTGTTATTTCTGGTTTCTACATGAGGTTAAGACCCTAGTTAAAACCTGTCGGAAAATAAGGGTGACAGGCACGTAAACTCTCTTATGCCTTTAAAGAAAAACAACTTCATCGAGATTTTTCAACTACTCAGCTTGATA... |
Task1_train_38904 | This alteration occurs on Chromosome 7. Is it associated with a disease or is it a benign variant? | Benign | GCACCCAGCTATTTTTAAAAATGAAAAATCTAGGTGCCTATAGTTATAAGATTACAAAGAATCTTTTTCTAATTGTTAGAAAACCATTTTGTGTCAGAACACGTAGAAAGCAATCCTTTGCCCAAACCCTTCCTTTTTGCCCCTTGCCTTCTGGCTTGTCCTCAGCCCAGCCCCGTCCTGGGGTCACACAGCTCTGCCACCCTGCTCTGCAATCCCAAAGAGCCTTTCCAAGGCTGGAGAGCTGAGCCCCAAACAACAAATAGGTAAAGACAAAGGGAGCAGGAGGCCGTCGCTGGCCTCACTCACCTGTCTGAGGAACC... | GCACCCAGCTATTTTTAAAAATGAAAAATCTAGGTGCCTATAGTTATAAGATTACAAAGAATCTTTTTCTAATTGTTAGAAAACCATTTTGTGTCAGAACACGTAGAAAGCAATCCTTTGCCCAAACCCTTCCTTTTTGCCCCTTGCCTTCTGGCTTGTCCTCAGCCCAGCCCCGTCCTGGGGTCACACAGCTCTGCCACCCTGCTCTGCAATCCCAAAGAGCCTTTCCAAGGCTGGAGAGCTGAGCCCCAAACAACAAATAGGTAAAGACAAAGGGAGCAGGAGGCCGTCGCTGGCCTCACTCACCTGTCTGAGGAACC... |
Task1_train_38905 | A genetic alteration is present on Chromosome 7. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TGGTCTTGACCTTCTGACCTCAAGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGTCATGAGCCACCGCGCCTGGCCTACTTTACAGTCCTGAAGGTGACAGCTAGGCCTCACCTGTCCCCATATCTATGTAGGATGGCTCCTTTTGCCTGCAATGTGCTGACTACTTGTTCTGAGTGTTGGCCCTCAGAACTCGCCTCCCTGGGAGTGAGTGCCCTCCCTCGGTCTCCAGAACTCACTGCCTCTACCTGCCTCTAATGTGGTCCTGGAGAGTCGGCTTATGTCTCTGTTACCCCACTGCACTGAGACAA... | TGGTCTTGACCTTCTGACCTCAAGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGTCATGAGCCACCGCGCCTGGCCTACTTTACAGTCCTGAAGGTGACAGCTAGGCCTCACCTGTCCCCATATCTATGTAGGATGGCTCCTTTTGCCTGCAATGTGCTGACTACTTGTTCTGAGTGTTGGCCCTCAGAACTCGCCTCCCTGGGAGTGAGTGCCCTCCCTCGGTCTCCAGAACTCACTGCCTCTACCTGCCTCTAATGTGGTCCTGGAGAGTCGGCTTATGTCTCTGTTACCCCACTGCACTGAGACAA... |
Task1_train_38906 | A mutation is present on Chromosome 7. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CACATTTATATGTTCCCATGTTGGGTCCCCCTCATTACGTATTCAGCCAGTAAGGGCAGGATATTTGTGTCCGCTTTCCCAGGGTCCAGCACATGACCTAGCTTGATCAGTACATATTATTGAGCCTCGACAAATATGAGATTGGGCTCAAGAAATATTTATTGGGCTCAGTGAGTATTATTGAATGAATGAATATGGCCTTTCCGGAGCCTTTCCCCAAGGTCCAACACAATTGCCGAATTAATGCAGCCGAGGACACAGCATCCAGTTCCTACTCCTGCAGCCCAGTTACCCCCATCCAACACCACCCCCCTACCCAA... | CACATTTATATGTTCCCATGTTGGGTCCCCCTCATTACGTATTCAGCCAGTAAGGGCAGGATATTTGTGTCCGCTTTCCCAGGGTCCAGCACATGACCTAGCTTGATCAGTACATATTATTGAGCCTCGACAAATATGAGATTGGGCTCAAGAAATATTTATTGGGCTCAGTGAGTATTATTGAATGAATGAATATGGCCTTTCCGGAGCCTTTCCCCAAGGTCCAACACAATTGCCGAATTAATGCAGCCGAGGACACAGCATCCAGTTCCTACTCCTGCAGCCCAGTTACCCCCATCCAACACCACCCCCCTACCCAA... |
Task1_train_38907 | An alteration has been detected on Chromosome 7. Is it pathogenic, and if so, what disease is involved? | Benign | TCAGGCTGCGCGGGACACTGGGCAGAGTTTTTAAGGACAACTTGGTGGGTGGGGGAAGGCCAGTGAGTCGAGAGTGCTGATTGGTTGGGTCGGAGGTGAAATCTTAGGGAACTGAAGCTGTCCTCTTGTGCTGAGTTAGTTCCGGAGTGGGGGCCTAAGATCAGATGACCTGGTTTATCGATCTGGTAGGTGTCAGTTGATCCATCAAGTGCAGGGTCTGCAAAATATCTTGAGCACTGATCTTATTAGCAGTTTAGGGAGGGTCAGAATACTGTAGCCTTGCTGCCTGACTCCTAAATCATACTTTCTAATCTTTTGGT... | TCAGGCTGCGCGGGACACTGGGCAGAGTTTTTAAGGACAACTTGGTGGGTGGGGGAAGGCCAGTGAGTCGAGAGTGCTGATTGGTTGGGTCGGAGGTGAAATCTTAGGGAACTGAAGCTGTCCTCTTGTGCTGAGTTAGTTCCGGAGTGGGGGCCTAAGATCAGATGACCTGGTTTATCGATCTGGTAGGTGTCAGTTGATCCATCAAGTGCAGGGTCTGCAAAATATCTTGAGCACTGATCTTATTAGCAGTTTAGGGAGGGTCAGAATACTGTAGCCTTGCTGCCTGACTCCTAAATCATACTTTCTAATCTTTTGGT... |
Task1_train_38908 | A variant was discovered on Chromosome 7. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GAATGTGTAAATATCTTTTCAAGATCCTACTTTCAAATTTTAGAAAAGTTTTAAAAACATTTAATGTAGCCAGTAAGGTCTATACATTGTGTTCTTGCTTTCCAGTTTTTAAACATATGCCCCAAAGTAGGTTTTCTGGATCATATGGTATGTTTTTAGTTTTTGAGGAACTTCCATAGGAGCTGTACCATTTTATATGCCCACCAACAGTACACAAGGGGTCGTTTCTCTCATCCTCACCAACACTTGTCATTTTCTGTTTTGTTTTTAGTGGCCATCCTAATGGGTGTGAGGTGATGTCTCATTGTGGTTTTGATTGC... | GAATGTGTAAATATCTTTTCAAGATCCTACTTTCAAATTTTAGAAAAGTTTTAAAAACATTTAATGTAGCCAGTAAGGTCTATACATTGTGTTCTTGCTTTCCAGTTTTTAAACATATGCCCCAAAGTAGGTTTTCTGGATCATATGGTATGTTTTTAGTTTTTGAGGAACTTCCATAGGAGCTGTACCATTTTATATGCCCACCAACAGTACACAAGGGGTCGTTTCTCTCATCCTCACCAACACTTGTCATTTTCTGTTTTGTTTTTAGTGGCCATCCTAATGGGTGTGAGGTGATGTCTCATTGTGGTTTTGATTGC... |
Task1_train_38909 | Chromosome 7 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GACTAGCAAATTCCAGAAGGTTCTAACTATACTATTAGAAAGAATTAACTAGTAAAGGCCTTACCCTTCTGTTGGTCACACATTCCTCTCATGGAGAGTAAGCCCTTGCCACATCATTTATTATACTCCCATGGAGGACAAAGCACCTAAAATGCCAAGAAGTGGATGAGAGAAGAACTCTGGGATGCTTTTATCTGTATTTTGGAGATAATACTTGTTTCTATATTATAATTTTATTATTGTACTAAGATAAACGTATTCACTGACAAATGAATTTCATCCAGATCTTAGGTTCATAAATTTTTATTAATTTGTAGTCT... | GACTAGCAAATTCCAGAAGGTTCTAACTATACTATTAGAAAGAATTAACTAGTAAAGGCCTTACCCTTCTGTTGGTCACACATTCCTCTCATGGAGAGTAAGCCCTTGCCACATCATTTATTATACTCCCATGGAGGACAAAGCACCTAAAATGCCAAGAAGTGGATGAGAGAAGAACTCTGGGATGCTTTTATCTGTATTTTGGAGATAATACTTGTTTCTATATTATAATTTTATTATTGTACTAAGATAAACGTATTCACTGACAAATGAATTTCATCCAGATCTTAGGTTCATAAATTTTTATTAATTTGTAGTCT... |
Task1_train_38910 | A genomic change on Chromosome 7 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GGAGCTGCTGCAAATTAAAAGCTTCGTGTCCCAAAAGATCCAATTTATTTTGTGGTAATTTTGTAGACAAAGCTTCTAGGGTTGAGTCAAGGTACAGGTACATGGGAAGGAAGCCCAATGCATGTAGACTCCATAAGATACTTATTACAGTTCACTTATAGTTCCTTCCAGTCAAGATGCAATTTTCCAATCAAGAGTCTTTTTTTTTTTTGTTCTAGAAACATAGTTGATGTTCTTACCCTTATCATATAAGGATAAGATTATCCTTATCATCCTTATCATCATGATAAGGAAAACAGCTAGGAAGTTTAACCATAGGT... | GGAGCTGCTGCAAATTAAAAGCTTCGTGTCCCAAAAGATCCAATTTATTTTGTGGTAATTTTGTAGACAAAGCTTCTAGGGTTGAGTCAAGGTACAGGTACATGGGAAGGAAGCCCAATGCATGTAGACTCCATAAGATACTTATTACAGTTCACTTATAGTTCCTTCCAGTCAAGATGCAATTTTCCAATCAAGAGTCTTTTTTTTTTTTGTTCTAGAAACATAGTTGATGTTCTTACCCTTATCATATAAGGATAAGATTATCCTTATCATCCTTATCATCATGATAAGGAAAACAGCTAGGAAGTTTAACCATAGGT... |
Task1_train_38911 | A mutation on Chromosome 7 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TTATCATCCTTATCATCATGATAAGGAAAACAGCTAGGAAGTTTAACCATAGGTCAAATTCTCATGCATAGGGAGAAAGGGTTCTGCTAACACTTTTCCTATACTGACCCTTGTGGAAATAACTTCTAACTGAATGAGCTCATTCATTGATTGTGCTAGCCAACCTTATCACATCTTAATTATAGCACTTCCTCCTACAGAGAACCCAACAATTTGGTATAGTACATTCTAGATAGAGTTTGTTACTATCTAATTCTGGGATTCCTGCTCTTTTGGCCACATTTATCTGTTATGGCTTACTCTATATCATTTATTCTATT... | TTATCATCCTTATCATCATGATAAGGAAAACAGCTAGGAAGTTTAACCATAGGTCAAATTCTCATGCATAGGGAGAAAGGGTTCTGCTAACACTTTTCCTATACTGACCCTTGTGGAAATAACTTCTAACTGAATGAGCTCATTCATTGATTGTGCTAGCCAACCTTATCACATCTTAATTATAGCACTTCCTCCTACAGAGAACCCAACAATTTGGTATAGTACATTCTAGATAGAGTTTGTTACTATCTAATTCTGGGATTCCTGCTCTTTTGGCCACATTTATCTGTTATGGCTTACTCTATATCATTTATTCTATT... |
Task1_train_38912 | This is a variant located on Chromosome 7. Is this mutation a likely cause of disease or not? | Benign | GTACCCAAGATCTTAGCCACAAGTGAGAGCTTCAAGCCCTTTGAGTGGAAAGAGAGGGAGGCAAATAAATAGGAGCCAACATCTTTTATGATGCTGTAGACTCCCATATAACACTGAGGCTAATAACAAGGAATTTAGAATCTGACAATTTTGGGTTCCATTTCAGGCTCTGATATCCACCAGCTATGGGCAATGTTAAATAACCTCTTTTAGCCTGCATTTTCTCATGTGTAAAGTTGGAACAAAAGATAACCTCAAAGGTTTGTTATGAGCATTAAATGAGATAACGAATGTAATCCCGGACAGTGTAGTAAATGTTC... | GTACCCAAGATCTTAGCCACAAGTGAGAGCTTCAAGCCCTTTGAGTGGAAAGAGAGGGAGGCAAATAAATAGGAGCCAACATCTTTTATGATGCTGTAGACTCCCATATAACACTGAGGCTAATAACAAGGAATTTAGAATCTGACAATTTTGGGTTCCATTTCAGGCTCTGATATCCACCAGCTATGGGCAATGTTAAATAACCTCTTTTAGCCTGCATTTTCTCATGTGTAAAGTTGGAACAAAAGATAACCTCAAAGGTTTGTTATGAGCATTAAATGAGATAACGAATGTAATCCCGGACAGTGTAGTAAATGTTC... |
Task1_train_38913 | The following genetic variant occurs on Chromosome 7. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | ACTCTTATAAATCAATAATAAAAAGATAACTCAATATTAAAATGGGCAAACAAATAGTTACTTTATAATAGAAAAAATACAAATAGCCAAGAAGCACACAAAATTGTTCTCCATATCATCAGTTAGAAGACAAATGCAAATGGAAACCACAATGAGATACCATTTCATCCCCACTAGAATGGCCAAAATCAAAAAGACTGACAACACCAAATGTTGGTGGGAATGTGGAACAGCTCTCCTACATTATTGAGGGGAGCATAAAATGTCAGAATCACTCTGGAAAACTCTTTAACAGTTTTTATAAAGTTAAATGAATATAA... | ACTCTTATAAATCAATAATAAAAAGATAACTCAATATTAAAATGGGCAAACAAATAGTTACTTTATAATAGAAAAAATACAAATAGCCAAGAAGCACACAAAATTGTTCTCCATATCATCAGTTAGAAGACAAATGCAAATGGAAACCACAATGAGATACCATTTCATCCCCACTAGAATGGCCAAAATCAAAAAGACTGACAACACCAAATGTTGGTGGGAATGTGGAACAGCTCTCCTACATTATTGAGGGGAGCATAAAATGTCAGAATCACTCTGGAAAACTCTTTAACAGTTTTTATAAAGTTAAATGAATATAA... |
Task1_train_38914 | Given a variant located on Chromosome 7, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AATTGTTCTCCATATCATCAGTTAGAAGACAAATGCAAATGGAAACCACAATGAGATACCATTTCATCCCCACTAGAATGGCCAAAATCAAAAAGACTGACAACACCAAATGTTGGTGGGAATGTGGAACAGCTCTCCTACATTATTGAGGGGAGCATAAAATGTCAGAATCACTCTGGAAAACTCTTTAACAGTTTTTATAAAGTTAAATGAATATAAATTTTTTAACACAGTAATTTCACTCCTAGGTATTTACCTGAGAAATGAACCTATGCCTACAAAGAAATGGATTCAAGAATGTGTATAGAAACTTTATTCAT... | AATTGTTCTCCATATCATCAGTTAGAAGACAAATGCAAATGGAAACCACAATGAGATACCATTTCATCCCCACTAGAATGGCCAAAATCAAAAAGACTGACAACACCAAATGTTGGTGGGAATGTGGAACAGCTCTCCTACATTATTGAGGGGAGCATAAAATGTCAGAATCACTCTGGAAAACTCTTTAACAGTTTTTATAAAGTTAAATGAATATAAATTTTTTAACACAGTAATTTCACTCCTAGGTATTTACCTGAGAAATGAACCTATGCCTACAAAGAAATGGATTCAAGAATGTGTATAGAAACTTTATTCAT... |
Task1_train_38915 | A mutation on Chromosome 7 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GTGCAGCCAAGAGCGAGGACCTAGGTCTTTAAGGGAATCCTGGGACAACTTCAGTGTCCACCAAGGAAAGGAAGCCAGATGAAGTTGCAAATTTTGTAGCCACTGCAGGTGAAGAAATGGCTAATTTTTGGAGGAAAACTGAGGTGAAGATCTGGATCTATTAAGACCAAGTGCCTGAGAGGAGGAAACAGTTCTCTGGCCCCACAGCTGGCAGAACTAAGAGCCTTGGTGGTGAGCTGCTACAACTGTGAAGCCTGTGAACCACGAAGCCTATCAAGATTTAAATGTCTGGTATACCTTGTTTTCTCCTGAGTCTTTCA... | GTGCAGCCAAGAGCGAGGACCTAGGTCTTTAAGGGAATCCTGGGACAACTTCAGTGTCCACCAAGGAAAGGAAGCCAGATGAAGTTGCAAATTTTGTAGCCACTGCAGGTGAAGAAATGGCTAATTTTTGGAGGAAAACTGAGGTGAAGATCTGGATCTATTAAGACCAAGTGCCTGAGAGGAGGAAACAGTTCTCTGGCCCCACAGCTGGCAGAACTAAGAGCCTTGGTGGTGAGCTGCTACAACTGTGAAGCCTGTGAACCACGAAGCCTATCAAGATTTAAATGTCTGGTATACCTTGTTTTCTCCTGAGTCTTTCA... |
Task1_train_38916 | A genomic change on Chromosome 7 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TCTGTGTGTGTGTGTGTGTGTGTGCATGTAATTGTTTTATTGTACATTTTCAGTATATTTATATATGCTGGGGATAAATTCTCCTCTGCCCTTTCATGCCCAAGTGCAAGCCGGCCATCGTAGCTTTTTGATTCCCTTCACAGCCAAGTAAGTCCCTTTAAACAACAGCTCACACACTGAGTGTCCACTTTCTCACCTCCCACACACTCTGCAGCTGACTGTGGTCTCCTTCCTTCCCCCCTCACTTCCCTGATACCGCTCTGGCAAAAAGCACCCGTTACTTTCTCACTGGTAAGTCCAGCGGAACTGTTTCATACCTC... | TCTGTGTGTGTGTGTGTGTGTGTGCATGTAATTGTTTTATTGTACATTTTCAGTATATTTATATATGCTGGGGATAAATTCTCCTCTGCCCTTTCATGCCCAAGTGCAAGCCGGCCATCGTAGCTTTTTGATTCCCTTCACAGCCAAGTAAGTCCCTTTAAACAACAGCTCACACACTGAGTGTCCACTTTCTCACCTCCCACACACTCTGCAGCTGACTGTGGTCTCCTTCCTTCCCCCCTCACTTCCCTGATACCGCTCTGGCAAAAAGCACCCGTTACTTTCTCACTGGTAAGTCCAGCGGAACTGTTTCATACCTC... |
Task1_train_38917 | A mutation located on Chromosome 7 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TGTGATTATATTTGTAACTTTATATGCATTATTGGCTATAGGTGAGTACATTTCTATTTATGATTTCATCGATGTTTTCAAAAGGAGGCATTAATATAGCAGCTAGTGTTTCTGAACACAGTTTTTAAATGCCTGTGTGTTTTTATGATCGTTTTAAATTAGAGGATTATCCAAATAATGTTGTACTTCTTCAGCACACACTAGTAGAGAAAGCAGAGAGGCATTTATGGCAGTGGGGGGTATCCGGTCTGGAATGGAATATTTGAGTGACTTGAGAATCTGTGTATACTCATATACCTTTATGCATACTTGGACTTAAT... | TGTGATTATATTTGTAACTTTATATGCATTATTGGCTATAGGTGAGTACATTTCTATTTATGATTTCATCGATGTTTTCAAAAGGAGGCATTAATATAGCAGCTAGTGTTTCTGAACACAGTTTTTAAATGCCTGTGTGTTTTTATGATCGTTTTAAATTAGAGGATTATCCAAATAATGTTGTACTTCTTCAGCACACACTAGTAGAGAAAGCAGAGAGGCATTTATGGCAGTGGGGGGTATCCGGTCTGGAATGGAATATTTGAGTGACTTGAGAATCTGTGTATACTCATATACCTTTATGCATACTTGGACTTAAT... |
Task1_train_38918 | A mutation has occurred on Chromosome 7. What is the medical relevance of this mutation? | Benign | TCTGCACGTGCTTTACCCAGCCGGGCATGGGCAAGTGACTAGACTCATTGAGCAAATTTCTTGAAATTTGTCCAGAAAGCACTTAGCAGAGCTCATGGCACAAAGGGTTCTCACAGCTGAGTTTCTTAGTTTTTAGGCTTGTGTGAATTCCATCACAGGAATTTCTTGTGTCATCAGTGAGTGGAAATTACTGGCTTCCCCTTATCATGGAGCTGATGGACTTTGGAGTTACACTTGGGTTCATATCTTGGCTCCAGAAATTGTTCTCTCTAGGAGTTTTGTGACTTTTCACAGATTATGTGATATTTCCAAATCTCAGT... | TCTGCACGTGCTTTACCCAGCCGGGCATGGGCAAGTGACTAGACTCATTGAGCAAATTTCTTGAAATTTGTCCAGAAAGCACTTAGCAGAGCTCATGGCACAAAGGGTTCTCACAGCTGAGTTTCTTAGTTTTTAGGCTTGTGTGAATTCCATCACAGGAATTTCTTGTGTCATCAGTGAGTGGAAATTACTGGCTTCCCCTTATCATGGAGCTGATGGACTTTGGAGTTACACTTGGGTTCATATCTTGGCTCCAGAAATTGTTCTCTCTAGGAGTTTTGTGACTTTTCACAGATTATGTGATATTTCCAAATCTCAGT... |
Task1_train_38919 | The following genetic variant occurs on Chromosome 7. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TCTTTGCAATGTTCTGGTAGAAAAGAGAAGGAAAAACAATGGCTTGGCCTTGGAGACTCTTGTCCCTCTAATCCAATATGTAGATTAAAAATTAATTATTTATTTGGTAGTCAAATATTTTGTTGGCAAATAAAGATTGAATATATTTAAGGTGGACGATGTGAGGATTTAATATATGTAGGCATAGTATAATGATTACCACAGCTATTTTAATGAACACATCCATCACTACCAATGCTGCAGACTGGATCCCCAGAACTTATTCATCTAAGAACTGAAAGTTTGTACCCTTGACCATCATCTCCCCATTTTCCACTTCT... | TCTTTGCAATGTTCTGGTAGAAAAGAGAAGGAAAAACAATGGCTTGGCCTTGGAGACTCTTGTCCCTCTAATCCAATATGTAGATTAAAAATTAATTATTTATTTGGTAGTCAAATATTTTGTTGGCAAATAAAGATTGAATATATTTAAGGTGGACGATGTGAGGATTTAATATATGTAGGCATAGTATAATGATTACCACAGCTATTTTAATGAACACATCCATCACTACCAATGCTGCAGACTGGATCCCCAGAACTTATTCATCTAAGAACTGAAAGTTTGTACCCTTGACCATCATCTCCCCATTTTCCACTTCT... |
Task1_train_38920 | A variant was discovered on Chromosome 7. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | AAGAAGAATTCCTATGGTGTCCACCCCTACTACATGGGGCTAGAGGAGGATGGCAGTGCCCATGGAGTGCTCCTGCTGAACAGCAATGCCATGGGTAAGGCCATCCAGCGCCTCCCTTATTTTGGGGGGATACCAGTCATGCCTGAGTCAGTTTAGAATGTGTTTAGCCTAACTGTTCCTTGAAGTCAAAATCTTCATTTTACGGGCACTGCTGTTTATTTTTTCTTTGTGTTTAGCCTTTCTGTTCATTTCAGTCTAATATCATGTGATAAGAAGATTTAACCCAACTCTTATTTTGGTAAAAATCACATAAGAAGGGA... | AAGAAGAATTCCTATGGTGTCCACCCCTACTACATGGGGCTAGAGGAGGATGGCAGTGCCCATGGAGTGCTCCTGCTGAACAGCAATGCCATGGGTAAGGCCATCCAGCGCCTCCCTTATTTTGGGGGGATACCAGTCATGCCTGAGTCAGTTTAGAATGTGTTTAGCCTAACTGTTCCTTGAAGTCAAAATCTTCATTTTACGGGCACTGCTGTTTATTTTTTCTTTGTGTTTAGCCTTTCTGTTCATTTCAGTCTAATATCATGTGATAAGAAGATTTAACCCAACTCTTATTTTGGTAAAAATCACATAAGAAGGGA... |
Task1_train_38921 | Chromosome 7 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | ATGACTTTTCTTCTGTTTTGCTGATAGGGCATGATTAATCTGTATGGAGCTCATACATTCTTCTTGTGCCTTGAAGATGCCAGGGGCTCCTCTTTTGGAGTATTTCTGATGAACAGTAATGCCATGGGTAGGAAGCATCTTTTTATCTTCTGTAGGTAGGAATACGTTTTAGGATTCTGCTTTTATAAAAAATTACTTTTATGGTGAGATCAACTGTTGAACAGAAGGCATTTTGAACCTACAATACTTTTATTGAAACTGGAACCTGAAAGTAGGTTAATCTGTCTACAAATCCAGGTGATACTTGACATTGTTTTCAT... | ATGACTTTTCTTCTGTTTTGCTGATAGGGCATGATTAATCTGTATGGAGCTCATACATTCTTCTTGTGCCTTGAAGATGCCAGGGGCTCCTCTTTTGGAGTATTTCTGATGAACAGTAATGCCATGGGTAGGAAGCATCTTTTTATCTTCTGTAGGTAGGAATACGTTTTAGGATTCTGCTTTTATAAAAAATTACTTTTATGGTGAGATCAACTGTTGAACAGAAGGCATTTTGAACCTACAATACTTTTATTGAAACTGGAACCTGAAAGTAGGTTAATCTGTCTACAAATCCAGGTGATACTTGACATTGTTTTCAT... |
Task1_train_38922 | This variant is present on Chromosome 7. Is the change likely to result in a pathogenic outcome? | Benign | ATAGAAAAGAGAAAACTAAAAGACAGAAAATACAAAGCCTCTGAGTAAGACTGTTCCTTTAAGATGTTTAAAAAAAAAAAAAAACCCAGCAGTTATCTAATCTGTTTTACCACAGTACCAGCCTGCCTCTAAATAAACTGGAACCACAGATATCTTCAACCCTGTTTTGGTTTCACTCTGTGTAAGCTGAATGTGTTTCTTTCATGATTGATTACTGCAGAGTATAATAAACCTGCAGCCAGTGGTAATAAAAGCAAAGTGTCGGCCAGTCTACATTAAAGTAGAAGTGGGGATAGGAGTTGAGTGAGTCCTCTCCTCCA... | ATAGAAAAGAGAAAACTAAAAGACAGAAAATACAAAGCCTCTGAGTAAGACTGTTCCTTTAAGATGTTTAAAAAAAAAAAAAAACCCAGCAGTTATCTAATCTGTTTTACCACAGTACCAGCCTGCCTCTAAATAAACTGGAACCACAGATATCTTCAACCCTGTTTTGGTTTCACTCTGTGTAAGCTGAATGTGTTTCTTTCATGATTGATTACTGCAGAGTATAATAAACCTGCAGCCAGTGGTAATAAAAGCAAAGTGTCGGCCAGTCTACATTAAAGTAGAAGTGGGGATAGGAGTTGAGTGAGTCCTCTCCTCCA... |
Task1_train_38923 | This alteration on Chromosome 7 may affect genome function. Does it lead to a disease or is it benign? | Benign | TAAGCATAAAAGGAATTGTCATCTCCCATCTCTTGTCCTGCTGCTGAATAGAATGAAGTGAAAGTCTGGATTTTGCCTGGGGTGAGGTTCCCTATCCCAGTAGAAGCTGTCACCTGTGTGTGCACCTTTGCCTTCCTGTGTATGTCTTCTCTCTTGGGCTGTGTGAGTGATTTCCTCTCTGTTGCCCTCTTTGGTAAGAAGTCCTTTGGCCAACTCAAGAGAAGTTGTTCTAAGAGTTTCATGCTTTTCTATTGGAAAGTTTGCTTAAACTCTATTTGTTTATTTATATATTTACTCAAGCTGATATTCCAGGCACTGAG... | TAAGCATAAAAGGAATTGTCATCTCCCATCTCTTGTCCTGCTGCTGAATAGAATGAAGTGAAAGTCTGGATTTTGCCTGGGGTGAGGTTCCCTATCCCAGTAGAAGCTGTCACCTGTGTGTGCACCTTTGCCTTCCTGTGTATGTCTTCTCTCTTGGGCTGTGTGAGTGATTTCCTCTCTGTTGCCCTCTTTGGTAAGAAGTCCTTTGGCCAACTCAAGAGAAGTTGTTCTAAGAGTTTCATGCTTTTCTATTGGAAAGTTTGCTTAAACTCTATTTGTTTATTTATATATTTACTCAAGCTGATATTCCAGGCACTGAG... |
Task1_train_38924 | A mutation found on Chromosome 7 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TCTGACTAAATGAAGTGAAAAGAAAAGATTTCCAGCATAGGGATTATGCACACAGAGCATCTCTCTGTATTTATCTGACCAAAATCAACATGACCTAACCCAAAAAGGAATGTTTATATCCTATTACTGGAAAGGAATGAATCCATCATTTTTTGTTAAATTGTAATTTAAGAGGTGAGCTACATGTGAGGTTTAAGAAGTTCTAAAATACCCATTTATATCTCTTCTTTTCTGGCAGATACTAACTATTCAATTGACTGACAAGACTATCAACCTGGAAAAGTTAACTGAGGTTACTTGGATTGATGGTGGTCCTGTAC... | TCTGACTAAATGAAGTGAAAAGAAAAGATTTCCAGCATAGGGATTATGCACACAGAGCATCTCTCTGTATTTATCTGACCAAAATCAACATGACCTAACCCAAAAAGGAATGTTTATATCCTATTACTGGAAAGGAATGAATCCATCATTTTTTGTTAAATTGTAATTTAAGAGGTGAGCTACATGTGAGGTTTAAGAAGTTCTAAAATACCCATTTATATCTCTTCTTTTCTGGCAGATACTAACTATTCAATTGACTGACAAGACTATCAACCTGGAAAAGTTAACTGAGGTTACTTGGATTGATGGTGGTCCTGTAC... |
Task1_train_38925 | Here is a genetic alteration on Chromosome 7. Based on the data, is it a benign variant or a cause of disease? | Benign | AAACAGAATCACTAAAAGTACTATGGAGAGGAGGATTTATGACAGGAGTTAGACCTTATATAAATGTAGGGGGAGCTGAGGAAGAGAAGGTCTGGAGGGGAGATATAGCTAGGCAGATTTAATTCATGATTAATGTGACCGTGACCTCTTATTCTACTCAAAGGAGAGCATATGATTTCAACAAAAAAAATATTGATTTTCCTTTGTAAAAGTTTGATCCAAATAGTGAGCTATTTTTGTCCCATAATTGTCTTAAGTTGGCTAATGGTGGAACAAATCCGACTTTGATTTCCTTGAAAGAACAGGAAAAAAACCATCAT... | AAACAGAATCACTAAAAGTACTATGGAGAGGAGGATTTATGACAGGAGTTAGACCTTATATAAATGTAGGGGGAGCTGAGGAAGAGAAGGTCTGGAGGGGAGATATAGCTAGGCAGATTTAATTCATGATTAATGTGACCGTGACCTCTTATTCTACTCAAAGGAGAGCATATGATTTCAACAAAAAAAATATTGATTTTCCTTTGTAAAAGTTTGATCCAAATAGTGAGCTATTTTTGTCCCATAATTGTCTTAAGTTGGCTAATGGTGGAACAAATCCGACTTTGATTTCCTTGAAAGAACAGGAAAAAAACCATCAT... |
Task1_train_38926 | This mutation is located on Chromosome 7. Is it associated with a disease or is it a benign polymorphism? | Benign | AATTATACAATGTAAACATTATACATTTTAAATGAACAGATCAGTGATTTTTGAGCAATATATATGTATATGCCCTTATAATCCCCACCCCTCTTAAAATGTAAAATATCCCCACCCCTATTAAAATGTAGAATATCTCCAGAAAGTTCCCTCGAACACCTCTGCAATGCCTATCTTGGTCCCAGAAAACCAATGATGTAACTTCTATCACTGGAGAGTAGTTTTGTTCACAAATATTTTTAATGTCAATTTAAAACCCATACTGATTAATCCTCTTGAATACATAGCTAAATAATCAAGGCAAGGAAGAGTTTCTGGGA... | AATTATACAATGTAAACATTATACATTTTAAATGAACAGATCAGTGATTTTTGAGCAATATATATGTATATGCCCTTATAATCCCCACCCCTCTTAAAATGTAAAATATCCCCACCCCTATTAAAATGTAGAATATCTCCAGAAAGTTCCCTCGAACACCTCTGCAATGCCTATCTTGGTCCCAGAAAACCAATGATGTAACTTCTATCACTGGAGAGTAGTTTTGTTCACAAATATTTTTAATGTCAATTTAAAACCCATACTGATTAATCCTCTTGAATACATAGCTAAATAATCAAGGCAAGGAAGAGTTTCTGGGA... |
Task1_train_38927 | A variant was discovered on Chromosome 7. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | AGTTCCCTCGAACACCTCTGCAATGCCTATCTTGGTCCCAGAAAACCAATGATGTAACTTCTATCACTGGAGAGTAGTTTTGTTCACAAATATTTTTAATGTCAATTTAAAACCCATACTGATTAATCCTCTTGAATACATAGCTAAATAATCAAGGCAAGGAAGAGTTTCTGGGAGGTTTTATGGTTTTAGAAGGGATTGAAACCATGAGAGCTACCTTGATCCATGGTAGGAACGATTCTATCTGGAGATGGATGTTGTGCCGAAATAACCTCAAAAGGTCTTTTCAGCTGGTAGAAGCTGATTCGACAACATTTATT... | AGTTCCCTCGAACACCTCTGCAATGCCTATCTTGGTCCCAGAAAACCAATGATGTAACTTCTATCACTGGAGAGTAGTTTTGTTCACAAATATTTTTAATGTCAATTTAAAACCCATACTGATTAATCCTCTTGAATACATAGCTAAATAATCAAGGCAAGGAAGAGTTTCTGGGAGGTTTTATGGTTTTAGAAGGGATTGAAACCATGAGAGCTACCTTGATCCATGGTAGGAACGATTCTATCTGGAGATGGATGTTGTGCCGAAATAACCTCAAAAGGTCTTTTCAGCTGGTAGAAGCTGATTCGACAACATTTATT... |
Task1_train_38928 | This variant is located on Chromosome 7. Evaluate its biological effect and specify any disease association. | Benign | ATGGCCTTATAGTTGCTAATTTGTGGAGAAGGCATCATATAAAAGTAAGAGAAAATCAGAATTGTGTTCTAGAGGGTAAATTGTGGCTGTCCTGAGAGCATGTTCCCCAGGAACCTAAACCATGAGCATGTTCAGGAACCCAGAGTGCAACAGACAATTCTTGGCCCCATGAATTTGGTGGTAAGACTGGAGACAGTTGGAAAAACCATGGAGTCTTGAAGTTCTTCACTCTCAATGCAGGCCTCTCTTGAACACCACAGACTAATGTCAGATAAATATGCTTCCACTATTAAGACTATTAAAACAAGAACCAATGAAGA... | ATGGCCTTATAGTTGCTAATTTGTGGAGAAGGCATCATATAAAAGTAAGAGAAAATCAGAATTGTGTTCTAGAGGGTAAATTGTGGCTGTCCTGAGAGCATGTTCCCCAGGAACCTAAACCATGAGCATGTTCAGGAACCCAGAGTGCAACAGACAATTCTTGGCCCCATGAATTTGGTGGTAAGACTGGAGACAGTTGGAAAAACCATGGAGTCTTGAAGTTCTTCACTCTCAATGCAGGCCTCTCTTGAACACCACAGACTAATGTCAGATAAATATGCTTCCACTATTAAGACTATTAAAACAAGAACCAATGAAGA... |
Task1_train_38929 | This is a variant located on Chromosome 7. Is this mutation a likely cause of disease or not? | Benign | CTTGAAGTTCTTCACTCTCAATGCAGGCCTCTCTTGAACACCACAGACTAATGTCAGATAAATATGCTTCCACTATTAAGACTATTAAAACAAGAACCAATGAAGAGAAGTGAGCAGAAACAATAAGCAATTGAAGTGTTTGAAGACAAGAAATTTTTACCATTAAAAGGTATGAAAGTTTGTAGAACTATATTTAAAGGAAATTGAAATGTGAACAAGAAAAAAAGACTGACAGAAACCATCAAGATAACATTAAAAAAAAATCAAATTCAATACAGAAATGATTAAGATTATCACTGAAAACAAAATGGAAATGAAGA... | CTTGAAGTTCTTCACTCTCAATGCAGGCCTCTCTTGAACACCACAGACTAATGTCAGATAAATATGCTTCCACTATTAAGACTATTAAAACAAGAACCAATGAAGAGAAGTGAGCAGAAACAATAAGCAATTGAAGTGTTTGAAGACAAGAAATTTTTACCATTAAAAGGTATGAAAGTTTGTAGAACTATATTTAAAGGAAATTGAAATGTGAACAAGAAAAAAAGACTGACAGAAACCATCAAGATAACATTAAAAAAAAATCAAATTCAATACAGAAATGATTAAGATTATCACTGAAAACAAAATGGAAATGAAGA... |
Task1_train_38930 | A variant on Chromosome 7 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TCTTCACTCTCAATGCAGGCCTCTCTTGAACACCACAGACTAATGTCAGATAAATATGCTTCCACTATTAAGACTATTAAAACAAGAACCAATGAAGAGAAGTGAGCAGAAACAATAAGCAATTGAAGTGTTTGAAGACAAGAAATTTTTACCATTAAAAGGTATGAAAGTTTGTAGAACTATATTTAAAGGAAATTGAAATGTGAACAAGAAAAAAAGACTGACAGAAACCATCAAGATAACATTAAAAAAAAATCAAATTCAATACAGAAATGATTAAGATTATCACTGAAAACAAAATGGAAATGAAGAAAGATGAA... | TCTTCACTCTCAATGCAGGCCTCTCTTGAACACCACAGACTAATGTCAGATAAATATGCTTCCACTATTAAGACTATTAAAACAAGAACCAATGAAGAGAAGTGAGCAGAAACAATAAGCAATTGAAGTGTTTGAAGACAAGAAATTTTTACCATTAAAAGGTATGAAAGTTTGTAGAACTATATTTAAAGGAAATTGAAATGTGAACAAGAAAAAAAGACTGACAGAAACCATCAAGATAACATTAAAAAAAAATCAAATTCAATACAGAAATGATTAAGATTATCACTGAAAACAAAATGGAAATGAAGAAAGATGAA... |
Task1_train_38931 | This mutation occurs on Chromosome 7. Does this change lead to a known medical condition, or is it benign? | Benign | AGCTGGTTGCTTGCTTGGCAAAAAAATGAATTCACCAATTGGCCAATCTGCTGAAAGTCAAAATGAAAGGCTAATATATGAGACTGATGACAGTTCATGGTTCTTGGTATAACTTCAACAGCGAGTGAGCATTTTTTTCTTTGTCTATAGCTTTCTTTCAGCCATCGATCCTCAGTTGTGTCTTAGCCTCTTATCAGTCCAGCTCACTTTGATACTAAATTTGATTGTTGTGTATCTCAGCAAGAAGCACGTCTCACATTCTCTGTATTTTTTGTGGTCATGAGTGTGTTCCTGTCTTATTCTTATTTTATGTGGTGCAT... | AGCTGGTTGCTTGCTTGGCAAAAAAATGAATTCACCAATTGGCCAATCTGCTGAAAGTCAAAATGAAAGGCTAATATATGAGACTGATGACAGTTCATGGTTCTTGGTATAACTTCAACAGCGAGTGAGCATTTTTTTCTTTGTCTATAGCTTTCTTTCAGCCATCGATCCTCAGTTGTGTCTTAGCCTCTTATCAGTCCAGCTCACTTTGATACTAAATTTGATTGTTGTGTATCTCAGCAAGAAGCACGTCTCACATTCTCTGTATTTTTTGTGGTCATGAGTGTGTTCCTGTCTTATTCTTATTTTATGTGGTGCAT... |
Task1_train_38932 | Chromosome 7 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CAGTTCATGGTTCTTGGTATAACTTCAACAGCGAGTGAGCATTTTTTTCTTTGTCTATAGCTTTCTTTCAGCCATCGATCCTCAGTTGTGTCTTAGCCTCTTATCAGTCCAGCTCACTTTGATACTAAATTTGATTGTTGTGTATCTCAGCAAGAAGCACGTCTCACATTCTCTGTATTTTTTGTGGTCATGAGTGTGTTCCTGTCTTATTCTTATTTTATGTGGTGCATTTCTAAATAGGACTGTACAGAATACAAGCATCTATTTGTATATGACTCTCATCTTTTATGGGGAGAGGTCAGAGTAGGTGAGCGTGCACT... | CAGTTCATGGTTCTTGGTATAACTTCAACAGCGAGTGAGCATTTTTTTCTTTGTCTATAGCTTTCTTTCAGCCATCGATCCTCAGTTGTGTCTTAGCCTCTTATCAGTCCAGCTCACTTTGATACTAAATTTGATTGTTGTGTATCTCAGCAAGAAGCACGTCTCACATTCTCTGTATTTTTTGTGGTCATGAGTGTGTTCCTGTCTTATTCTTATTTTATGTGGTGCATTTCTAAATAGGACTGTACAGAATACAAGCATCTATTTGTATATGACTCTCATCTTTTATGGGGAGAGGTCAGAGTAGGTGAGCGTGCACT... |
Task1_train_38933 | This genomic variant is located on Chromosome 7. Can you determine its pathogenicity and name any linked disease? | Benign | TCATCACCACGTAGCCAGTTGCCCTGTGGGAGGGCCCTGGAGCTGGTTCCAATGTCTTCCTTCTGGACTTATATCTCAATTCTCAAAACAGAGGAATTCATTTCACTGCTGATGGTAAACAGATAAAGGCTCTCCCATTTCCCCAAAGATACATTCTGCTTCCCTTGTATCTCTTTCTGACACTTACCGCCCAGATCCATTACCTTCTGTGATCAAACACCTCTTTGAATATTTCCTAAAACTCTGCAGCCTTTACATTCTCTGCATTTGTGCTCAGTATTTCCATGGCCTGGAAGGACCTTCTGTCTCCCAAGAAACAG... | TCATCACCACGTAGCCAGTTGCCCTGTGGGAGGGCCCTGGAGCTGGTTCCAATGTCTTCCTTCTGGACTTATATCTCAATTCTCAAAACAGAGGAATTCATTTCACTGCTGATGGTAAACAGATAAAGGCTCTCCCATTTCCCCAAAGATACATTCTGCTTCCCTTGTATCTCTTTCTGACACTTACCGCCCAGATCCATTACCTTCTGTGATCAAACACCTCTTTGAATATTTCCTAAAACTCTGCAGCCTTTACATTCTCTGCATTTGTGCTCAGTATTTCCATGGCCTGGAAGGACCTTCTGTCTCCCAAGAAACAG... |
Task1_train_38934 | A genetic alteration is present on Chromosome 7. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GGGCTCTGGCCTTTTCTTCCCTGAGCAGCATGATGATGCTCCATTCCTGTCTTGACAAGGATTCTGTCATGGATTTCTTGGTTGTGCTGCCCAGGAAGCAGGTGAGGCCCAGGAACAATGAGGAATGTCGTCCCTGGACTTGGCATGCCTCACTCGCAAGCACACCATATGTGGGTCCTGTGATTGATAGGTTTGATAGATGGATACGTCCTGTTTCCAGCCACCAGCCTCTATCCCCTGAATGCTGTTGTCAACTCAGAGCCACAACTCTGGTCACAAAGATGGAGCAAGTAGTGGCACCTTAATGTGAAGAAATTTTC... | GGGCTCTGGCCTTTTCTTCCCTGAGCAGCATGATGATGCTCCATTCCTGTCTTGACAAGGATTCTGTCATGGATTTCTTGGTTGTGCTGCCCAGGAAGCAGGTGAGGCCCAGGAACAATGAGGAATGTCGTCCCTGGACTTGGCATGCCTCACTCGCAAGCACACCATATGTGGGTCCTGTGATTGATAGGTTTGATAGATGGATACGTCCTGTTTCCAGCCACCAGCCTCTATCCCCTGAATGCTGTTGTCAACTCAGAGCCACAACTCTGGTCACAAAGATGGAGCAAGTAGTGGCACCTTAATGTGAAGAAATTTTC... |
Task1_train_38935 | A genomic change on Chromosome 7 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | AGGATTCTGTCATGGATTTCTTGGTTGTGCTGCCCAGGAAGCAGGTGAGGCCCAGGAACAATGAGGAATGTCGTCCCTGGACTTGGCATGCCTCACTCGCAAGCACACCATATGTGGGTCCTGTGATTGATAGGTTTGATAGATGGATACGTCCTGTTTCCAGCCACCAGCCTCTATCCCCTGAATGCTGTTGTCAACTCAGAGCCACAACTCTGGTCACAAAGATGGAGCAAGTAGTGGCACCTTAATGTGAAGAAATTTTCCATCATGCAATTGTTACCTGGTGCCTACATGAGTTAGACTCAAACCAGCAGCTGTTT... | AGGATTCTGTCATGGATTTCTTGGTTGTGCTGCCCAGGAAGCAGGTGAGGCCCAGGAACAATGAGGAATGTCGTCCCTGGACTTGGCATGCCTCACTCGCAAGCACACCATATGTGGGTCCTGTGATTGATAGGTTTGATAGATGGATACGTCCTGTTTCCAGCCACCAGCCTCTATCCCCTGAATGCTGTTGTCAACTCAGAGCCACAACTCTGGTCACAAAGATGGAGCAAGTAGTGGCACCTTAATGTGAAGAAATTTTCCATCATGCAATTGTTACCTGGTGCCTACATGAGTTAGACTCAAACCAGCAGCTGTTT... |
Task1_train_38936 | A variant on Chromosome 7 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GAAGCTTTCTGTACTTTGCCCATTTAGACACTACAAATTCTGATGTCTGACAAAAAGTGTAAACTTAAAGCTTGCATGTGGTTAAGAACTTTTAATAAACAAATTAAATAATATATATAATGAAAATGTCAATAATGCTCTCCAATCCAATCCCACCTTCCACTCATAACCAATATTAACGCTCTGGTGTGCTTCTTTTCACCCCTCTTTTCTGTGTTCATGCACACCTTTCTACCCAAGTACACCTACAGAAAATGGGTTCACCTGTACACTTTACCTGCCACATGCATACTCTTTTCTGTTAATATATCCTGGTCTTT... | GAAGCTTTCTGTACTTTGCCCATTTAGACACTACAAATTCTGATGTCTGACAAAAAGTGTAAACTTAAAGCTTGCATGTGGTTAAGAACTTTTAATAAACAAATTAAATAATATATATAATGAAAATGTCAATAATGCTCTCCAATCCAATCCCACCTTCCACTCATAACCAATATTAACGCTCTGGTGTGCTTCTTTTCACCCCTCTTTTCTGTGTTCATGCACACCTTTCTACCCAAGTACACCTACAGAAAATGGGTTCACCTGTACACTTTACCTGCCACATGCATACTCTTTTCTGTTAATATATCCTGGTCTTT... |
Task1_train_38937 | A mutation located on Chromosome 7 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CCATTGCATAAATATACTACAACTTGTTTATCCATGCTCCTGTTGATGGATATCCATGTTACTCCTGTCTTCAACTATTATGAATAAACTTGTTGTGAACATTTTTGTGGAATTCTTCCTGTGGACATATGCATTTTTTTTAAAGAAATAGACTTAAGAGTGGAAATACTGACTCATAGTGTAGATGTGTGTGCTATGCTTGCATGTCCTCACAAAATCTCATGTTGAAACTTGTCAAGGTAATGGTATTGGGAGGTGGGACAGCTATGACTAGGGTCATGAGGGATCTGCCCTCAGAAACAGATCAATGCCCTTTATTG... | CCATTGCATAAATATACTACAACTTGTTTATCCATGCTCCTGTTGATGGATATCCATGTTACTCCTGTCTTCAACTATTATGAATAAACTTGTTGTGAACATTTTTGTGGAATTCTTCCTGTGGACATATGCATTTTTTTTAAAGAAATAGACTTAAGAGTGGAAATACTGACTCATAGTGTAGATGTGTGTGCTATGCTTGCATGTCCTCACAAAATCTCATGTTGAAACTTGTCAAGGTAATGGTATTGGGAGGTGGGACAGCTATGACTAGGGTCATGAGGGATCTGCCCTCAGAAACAGATCAATGCCCTTTATTG... |
Task1_train_38938 | A genomic change on Chromosome 7 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TAAGTGGTCACTTCCTAACATGAAATGTAGAGGAAACCAATATTAACTAGAATCCATCTGATTTTAGTCAGTTTTCCTTTGTAAGTATTTGGAAGGTGGGATAATTTATTTTCAAGGTTAAGTAAACATCTATACATCTCCTTTATCTTTTGAAGACTGGTGGCGAAGCGAAAAATGGCACGGCCAATGGAGTCAGAGTTTGTTTAATAAATATCTCAGAGTTCAAAGAGAGACTCTCATGGGCCAGAAATTGGTAAATGTTCCTGCATTCTAAAATTAGGAGGATCTTATTTTCTTTGAATCAACAGAGAAGGAAGCAC... | TAAGTGGTCACTTCCTAACATGAAATGTAGAGGAAACCAATATTAACTAGAATCCATCTGATTTTAGTCAGTTTTCCTTTGTAAGTATTTGGAAGGTGGGATAATTTATTTTCAAGGTTAAGTAAACATCTATACATCTCCTTTATCTTTTGAAGACTGGTGGCGAAGCGAAAAATGGCACGGCCAATGGAGTCAGAGTTTGTTTAATAAATATCTCAGAGTTCAAAGAGAGACTCTCATGGGCCAGAAATTGGTAAATGTTCCTGCATTCTAAAATTAGGAGGATCTTATTTTCTTTGAATCAACAGAGAAGGAAGCAC... |
Task1_train_38939 | This variant lies on Chromosome 7. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AATAAATATCTCAGAGTTCAAAGAGAGACTCTCATGGGCCAGAAATTGGTAAATGTTCCTGCATTCTAAAATTAGGAGGATCTTATTTTCTTTGAATCAACAGAGAAGGAAGCACAGGCAGTGGGGAGGAACAGTTGGGAACACGGCAGAGTGGCCGCAGGATGTCAAAGACAAAGGACATGTAATATCAAATTCTAAGCTGTGAAGCTGTGATGCAACCCTCCACCTTCTCCTAATGGATTTTTTAGGTCTCAGCGCAGATGCACAGCTGAGGGAGTAATTTCTTTGGAAATGAAGGACAAATAGCTGTGTTAAATATT... | AATAAATATCTCAGAGTTCAAAGAGAGACTCTCATGGGCCAGAAATTGGTAAATGTTCCTGCATTCTAAAATTAGGAGGATCTTATTTTCTTTGAATCAACAGAGAAGGAAGCACAGGCAGTGGGGAGGAACAGTTGGGAACACGGCAGAGTGGCCGCAGGATGTCAAAGACAAAGGACATGTAATATCAAATTCTAAGCTGTGAAGCTGTGATGCAACCCTCCACCTTCTCCTAATGGATTTTTTAGGTCTCAGCGCAGATGCACAGCTGAGGGAGTAATTTCTTTGGAAATGAAGGACAAATAGCTGTGTTAAATATT... |
Task1_train_38940 | Mutation context: Chromosome 7. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TACCACAACTTGTTTATCCATGCTCCCGTTGATGGATATCCACATTACTCCTGTCTTCAACTATTATGAATACAGTTGTTGTGAACATTCTTGTGGAACTCTTTCTTGTGGACATATACATTCTTTTTTTTTATTTTATTTTAGGTATAAACTTAAGAGTGGAAATACTGACTTACAGTGTAGATGTGTGTGCTATGCTTGCGTGTCCTCACAAAAGCTCATGTTGAAATTTGTCATTGTAATGGTATTGGGAGGTGGGACAGCTATGACTAGGTCATGAGGGATCTGCCCTCAGAAAGAGATCAATGCCGTTATTGTGG... | TACCACAACTTGTTTATCCATGCTCCCGTTGATGGATATCCACATTACTCCTGTCTTCAACTATTATGAATACAGTTGTTGTGAACATTCTTGTGGAACTCTTTCTTGTGGACATATACATTCTTTTTTTTTATTTTATTTTAGGTATAAACTTAAGAGTGGAAATACTGACTTACAGTGTAGATGTGTGTGCTATGCTTGCGTGTCCTCACAAAAGCTCATGTTGAAATTTGTCATTGTAATGGTATTGGGAGGTGGGACAGCTATGACTAGGTCATGAGGGATCTGCCCTCAGAAAGAGATCAATGCCGTTATTGTGG... |
Task1_train_38941 | Given this variant on Chromosome 7, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GCGTGTCCTCACAAAAGCTCATGTTGAAATTTGTCATTGTAATGGTATTGGGAGGTGGGACAGCTATGACTAGGTCATGAGGGATCTGCCCTCAGAAAGAGATCAATGCCGTTATTGTGGGAGTGAATTAGTTGTCTTGGGAATGGTCTTCTGATAAAAAGTATAAATTCAGCCACTTTCTCTGTCTTGGGTGCTTGCTTCCCCTTCCTTCTGCCTTGGATAACAGCAGGAGGCCCTCAGCCGCTATGGCCCATTGATCTTGGACTTCCCAGTCTCCAGATCTATAAGCCAAATAAATGCCTTGTCTTTATAAATTACCC... | GCGTGTCCTCACAAAAGCTCATGTTGAAATTTGTCATTGTAATGGTATTGGGAGGTGGGACAGCTATGACTAGGTCATGAGGGATCTGCCCTCAGAAAGAGATCAATGCCGTTATTGTGGGAGTGAATTAGTTGTCTTGGGAATGGTCTTCTGATAAAAAGTATAAATTCAGCCACTTTCTCTGTCTTGGGTGCTTGCTTCCCCTTCCTTCTGCCTTGGATAACAGCAGGAGGCCCTCAGCCGCTATGGCCCATTGATCTTGGACTTCCCAGTCTCCAGATCTATAAGCCAAATAAATGCCTTGTCTTTATAAATTACCC... |
Task1_train_38942 | This variant lies on Chromosome 7. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GAAATGAGCAGCAACAGCACCACCACAGACACACACTCGCCAGGCACAGGGAGAGGACAGATCCTGGCCTCTTGTAGCACCAGAGCTCTGAACGCCCTCTACCTGCTCAGTCTCCCATGGGATCTAGGCTCTTCTCCTGGGCGCTGGACATGCCTTGGTTTCTCAAAACCAGGTGTGTCCTGGATGCACCTGGGGGAATCTCAGCTCTGAATATGCCAAGCCTTGCCAGAGGAACCATGTATTTTGAAAACCCACGGGGTCTGTGTTAAAAACAACAATTTCCCTCTCAGAGCATGATGGGATTCCATGTTCCTGCTTAG... | GAAATGAGCAGCAACAGCACCACCACAGACACACACTCGCCAGGCACAGGGAGAGGACAGATCCTGGCCTCTTGTAGCACCAGAGCTCTGAACGCCCTCTACCTGCTCAGTCTCCCATGGGATCTAGGCTCTTCTCCTGGGCGCTGGACATGCCTTGGTTTCTCAAAACCAGGTGTGTCCTGGATGCACCTGGGGGAATCTCAGCTCTGAATATGCCAAGCCTTGCCAGAGGAACCATGTATTTTGAAAACCCACGGGGTCTGTGTTAAAAACAACAATTTCCCTCTCAGAGCATGATGGGATTCCATGTTCCTGCTTAG... |
Task1_train_38943 | A mutation on Chromosome 7 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | TATATGATCATATCTATAGATAACTTAAGCATTTGATAAAATTCCATATCCTTTCTTGAAGAAAACTGTTATCAAACTCAAGAGTAACAAGAAATTTTCTTCACCTAAAAAAGGACATTTATGACATCCTATGGTTAAATAGAATATTTTTGCAAGCAAACTGATAAGTCAAAGATGCATATGTAATTCCCAGATCAAATACTAAAAACAGCAAAAAGAGGATAAAATAGCCTTTTCAGCAAATGGTTCTAGAAAAATGGGATAATATGGAAAAATAATGAATCTCTAGCCTTATCTCACTCCATAACCAGATGTGGGCA... | TATATGATCATATCTATAGATAACTTAAGCATTTGATAAAATTCCATATCCTTTCTTGAAGAAAACTGTTATCAAACTCAAGAGTAACAAGAAATTTTCTTCACCTAAAAAAGGACATTTATGACATCCTATGGTTAAATAGAATATTTTTGCAAGCAAACTGATAAGTCAAAGATGCATATGTAATTCCCAGATCAAATACTAAAAACAGCAAAAAGAGGATAAAATAGCCTTTTCAGCAAATGGTTCTAGAAAAATGGGATAATATGGAAAAATAATGAATCTCTAGCCTTATCTCACTCCATAACCAGATGTGGGCA... |
Task1_train_38944 | An alteration has been detected on Chromosome 7. Is it pathogenic, and if so, what disease is involved? | Benign | AATAGAATATTTTTGCAAGCAAACTGATAAGTCAAAGATGCATATGTAATTCCCAGATCAAATACTAAAAACAGCAAAAAGAGGATAAAATAGCCTTTTCAGCAAATGGTTCTAGAAAAATGGGATAATATGGAAAAATAATGAATCTCTAGCCTTATCTCACTCCATAACCAGATGTGGGCAAACTATGGCCTCCGGGCCAAATTTGGCCTTTGTCTGTTTTCATACAGCCCAGAAACTAACAAAAATTTTACACTTTTAAATGATTGAAAAAAAGTAAAAAGTATTTTGTTACATATAAAAATCTAAGATATTCAAAT... | AATAGAATATTTTTGCAAGCAAACTGATAAGTCAAAGATGCATATGTAATTCCCAGATCAAATACTAAAAACAGCAAAAAGAGGATAAAATAGCCTTTTCAGCAAATGGTTCTAGAAAAATGGGATAATATGGAAAAATAATGAATCTCTAGCCTTATCTCACTCCATAACCAGATGTGGGCAAACTATGGCCTCCGGGCCAAATTTGGCCTTTGTCTGTTTTCATACAGCCCAGAAACTAACAAAAATTTTACACTTTTAAATGATTGAAAAAAAGTAAAAAGTATTTTGTTACATATAAAAATCTAAGATATTCAAAT... |
Task1_train_38945 | A variant on Chromosome 7 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TGTTGGTTCTGTTTCTCTCTGAGGACGAGGTGGCCTAGATCCTTCCCTTTCTGGGTAAAGGGTGGAAGCAGTGTGGATCATTACTTAGTGTGTTCTGATAGCCATGTGTCACTATGTACTTGTTCTTTGTGTCTTCACATCTCTTCCTGTTGCATTTTAAAGCATTTTCATAGTATGTGGTGTTGCCTAGCAGAGCATTCTCATAGCAAAAAAATGTATATATATATACATATGCATATATATATTCTATTGGTTCTGTTTCTCTGGAGAAACGGTATATATATATATATATATATATATATATATATATATACTCTCCC... | TGTTGGTTCTGTTTCTCTCTGAGGACGAGGTGGCCTAGATCCTTCCCTTTCTGGGTAAAGGGTGGAAGCAGTGTGGATCATTACTTAGTGTGTTCTGATAGCCATGTGTCACTATGTACTTGTTCTTTGTGTCTTCACATCTCTTCCTGTTGCATTTTAAAGCATTTTCATAGTATGTGGTGTTGCCTAGCAGAGCATTCTCATAGCAAAAAAATGTATATATATATACATATGCATATATATATTCTATTGGTTCTGTTTCTCTGGAGAAACGGTATATATATATATATATATATATATATATATATATATACTCTCCC... |
Task1_train_38946 | A genetic alteration is present on Chromosome 7. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | CATATCCACGTATGAGGCATAGTCCAGTGTGTCTCCTGGAAGAAGATGAAGCCTGGGCAGACATAAGAATATGTTTTTGAATAGGCTTCCCTTGGCCTGATTTTAAATTCCTTCCATGTGATCATGCATCTGTCTGTACCTGTATTTTGTACCCGGCTTCTGCCTCTCACCCATCAGTCCCATGGCTACTAGAAGGTATTAAATTTCTATTGACAAAAATTACCACTAATTTGGTGGCTTACAACAATAAAAATTTATTATCTTACAGTTCTGGAGGTTAGAAGTCCAAAACCAGGCTAAAATCCAGGTATTGGCAGGGC... | CATATCCACGTATGAGGCATAGTCCAGTGTGTCTCCTGGAAGAAGATGAAGCCTGGGCAGACATAAGAATATGTTTTTGAATAGGCTTCCCTTGGCCTGATTTTAAATTCCTTCCATGTGATCATGCATCTGTCTGTACCTGTATTTTGTACCCGGCTTCTGCCTCTCACCCATCAGTCCCATGGCTACTAGAAGGTATTAAATTTCTATTGACAAAAATTACCACTAATTTGGTGGCTTACAACAATAAAAATTTATTATCTTACAGTTCTGGAGGTTAGAAGTCCAAAACCAGGCTAAAATCCAGGTATTGGCAGGGC... |
Task1_train_38947 | Chromosome 7 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | ACGTGAGAGTGGGACAGGGTCATCTCTGTGACAGTATAGTCACAGAAGCCTCTTCCTGCTCAAATAAGTGGCCTTCATTAAAAGAAACACAGAAGAATCTTGTTTCATAAGCTAATGCCAATCACTGAGACAGCAACGGTTTCAGGAACATGAGGGAAGCTGTTGGAATGGGCTTTCCTTTAAACCTAGCCTGGTTCCATCATGCTGATGTGGTGGGGGCTTTAAGTCAGGGCCTGAGAAGGACAGCCTAACTGTGGTATAAGTCAGAGGGCTCCTCATTCCTCATAAGCCGACAAATACATTAATATCATCAGAAAAAT... | ACGTGAGAGTGGGACAGGGTCATCTCTGTGACAGTATAGTCACAGAAGCCTCTTCCTGCTCAAATAAGTGGCCTTCATTAAAAGAAACACAGAAGAATCTTGTTTCATAAGCTAATGCCAATCACTGAGACAGCAACGGTTTCAGGAACATGAGGGAAGCTGTTGGAATGGGCTTTCCTTTAAACCTAGCCTGGTTCCATCATGCTGATGTGGTGGGGGCTTTAAGTCAGGGCCTGAGAAGGACAGCCTAACTGTGGTATAAGTCAGAGGGCTCCTCATTCCTCATAAGCCGACAAATACATTAATATCATCAGAAAAAT... |
Task1_train_38948 | A mutation on Chromosome 7 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | ACCCCGTCTATACTAAAAATACAAAAATTAGCTTGTAGTGGTGCGCGCTCGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGAAGAATCACTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCACCACTGCACTCCAGCCTGGCAATAGAGCAAGACTCAGTCTCCAACAACAAAAACAGAGTCTAAAATAGGCAAATTCTTAAAGACGGAAAATAGATTAATGATTGCCATGGGCTGTGGGAAGGAATAAAAGTGAAATGACATCTAATGATAAAGAATTTCTTTCTGGGGTGATAGAAATATTCTGGAATT... | ACCCCGTCTATACTAAAAATACAAAAATTAGCTTGTAGTGGTGCGCGCTCGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGAAGAATCACTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCACCACTGCACTCCAGCCTGGCAATAGAGCAAGACTCAGTCTCCAACAACAAAAACAGAGTCTAAAATAGGCAAATTCTTAAAGACGGAAAATAGATTAATGATTGCCATGGGCTGTGGGAAGGAATAAAAGTGAAATGACATCTAATGATAAAGAATTTCTTTCTGGGGTGATAGAAATATTCTGGAATT... |
Task1_train_38949 | Chromosome 7 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GGTATGCAAATTATATTTCAATTTTAAAGAAAATGTCAACACTCAACATGAAAATATTCAAAATTACAGCTCCAACATCAGAATAAAGACTATATTTTTGGATCTCTAGGATTCTGATATGAGTAAGACCATGAGTCATTATTATTTGGACACTAAATGTTAACATGATCTTATTTATTATTCAAGTCATACACCTAACTCCTCTGGGGTGCCTATCCAATGGAGTGAGATTGTGCCTTGTTTCCTGTATCTTTCTTTCACTACTCCTGGGACAAAGTAGACTTTCACATAATTTTTATTCAATGCTGCAGGATGAGAAA... | GGTATGCAAATTATATTTCAATTTTAAAGAAAATGTCAACACTCAACATGAAAATATTCAAAATTACAGCTCCAACATCAGAATAAAGACTATATTTTTGGATCTCTAGGATTCTGATATGAGTAAGACCATGAGTCATTATTATTTGGACACTAAATGTTAACATGATCTTATTTATTATTCAAGTCATACACCTAACTCCTCTGGGGTGCCTATCCAATGGAGTGAGATTGTGCCTTGTTTCCTGTATCTTTCTTTCACTACTCCTGGGACAAAGTAGACTTTCACATAATTTTTATTCAATGCTGCAGGATGAGAAA... |
Task1_train_38950 | A variant was discovered on Chromosome 7. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GCATTCTTTTAGGCATAATCCTTGTTCTGTTCCTTGCTGAGTACCCGTGCAGGTTTTTACGGATGCTAGGTTCAAGAATTCCTGCTATAAAATTATAGAACATCTGAGAGATGATGGAAATAGAGTTGGATAAATTTGTCTAGAATTTAGGGAAAAGGTCTGGCCCACAGATATTGTTCATTAGAAATGTGTCACCTCAACTTTTTGTCTTAATGTTTGTTTTTATTCTCATCACTCAACAGATATAGGCCACCTACAGAAAAAGATTTGTTATAATTTGCTTTGATGAAACAATTTCATAAAATCAAAAGGCAGACAAA... | GCATTCTTTTAGGCATAATCCTTGTTCTGTTCCTTGCTGAGTACCCGTGCAGGTTTTTACGGATGCTAGGTTCAAGAATTCCTGCTATAAAATTATAGAACATCTGAGAGATGATGGAAATAGAGTTGGATAAATTTGTCTAGAATTTAGGGAAAAGGTCTGGCCCACAGATATTGTTCATTAGAAATGTGTCACCTCAACTTTTTGTCTTAATGTTTGTTTTTATTCTCATCACTCAACAGATATAGGCCACCTACAGAAAAAGATTTGTTATAATTTGCTTTGATGAAACAATTTCATAAAATCAAAAGGCAGACAAA... |
Task1_train_38951 | Mutation context: Chromosome 7. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | GCTTATCTGTACATAACCCCATCATAAGTCAAGGAGCACACTGAAATGCATATTGCTTTTGCACCATTGTAAAGTTGAAAAGTCATTGAACCATCATGAGACCATCTGTACCTGACAATTAGTGTTTCTCAAAATAAATAGGAAGATTTTCTTCTGATCTGAAGGTCTTCCAGCCACTCCCTCCCAGACATATCATAATATTGGACCAGAGGTCACCCATAGCAAGCTGTCCCTACTTATTCTTTGCAGAAAAAGTACAGTTACAGTATGAAGTGGCCTCATTTTAATGAGGCCCAACATACCCAGGAAATAAAAAATGC... | GCTTATCTGTACATAACCCCATCATAAGTCAAGGAGCACACTGAAATGCATATTGCTTTTGCACCATTGTAAAGTTGAAAAGTCATTGAACCATCATGAGACCATCTGTACCTGACAATTAGTGTTTCTCAAAATAAATAGGAAGATTTTCTTCTGATCTGAAGGTCTTCCAGCCACTCCCTCCCAGACATATCATAATATTGGACCAGAGGTCACCCATAGCAAGCTGTCCCTACTTATTCTTTGCAGAAAAAGTACAGTTACAGTATGAAGTGGCCTCATTTTAATGAGGCCCAACATACCCAGGAAATAAAAAATGC... |
Task1_train_38952 | This sequence change occurs on Chromosome 7. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TATTTATATATTCAAGAAAAGCTAGTATATAAATTTTTTAAAAACCTACAAACTAATTTTTCTACAGATCAATGAGAAAAAGGTAACTGTCAATGGAAAAAGTGAGTGAAAACCATAAGCACCTAGCAAAATCTCACTGGTCATTAAACATGTAAATGTGGCTATATTTAATAATCAGGGAAATAGAAATTGAGTCCAACGAAATATATACCCACAAGAATGGCTACGATGATAAAAATAGTAACTATCAAGTGTTGGCAAGGCAAAGTGTCAACAAGAACTCTCTGAATCACTGGCTAGAGTGTATATCGGTAGATCCA... | TATTTATATATTCAAGAAAAGCTAGTATATAAATTTTTTAAAAACCTACAAACTAATTTTTCTACAGATCAATGAGAAAAAGGTAACTGTCAATGGAAAAAGTGAGTGAAAACCATAAGCACCTAGCAAAATCTCACTGGTCATTAAACATGTAAATGTGGCTATATTTAATAATCAGGGAAATAGAAATTGAGTCCAACGAAATATATACCCACAAGAATGGCTACGATGATAAAAATAGTAACTATCAAGTGTTGGCAAGGCAAAGTGTCAACAAGAACTCTCTGAATCACTGGCTAGAGTGTATATCGGTAGATCCA... |
Task1_train_38953 | This mutation occurs on Chromosome 7. Does this change lead to a known medical condition, or is it benign? | Benign | TGTTTATTAAGCCTACTTTGTATATGTTTGAAATTTTTAGAATTAAAAGTAAAAATATCTAAAAATAAGACTTTACCAATTTGACATGCAGCAGGAATGATTAGGGTAGGATGCCATGGTGTATCCATGCATGAGGGAGGGTCAGTGATATGGACAGGAGACGGAAATACTGGGTAGAAGAGGGTGGTTTCCCAGCAAAGGCCCCACCCTCAAGCCTGGAGACCTGCAGCTGTAAATGGGGACAAGCATTCCTGTTTTCATTCCCAAAAAGTTGTCTTTTGACCCACCATGCCCCCTTTCTTTTACCCATATAAACCCCA... | TGTTTATTAAGCCTACTTTGTATATGTTTGAAATTTTTAGAATTAAAAGTAAAAATATCTAAAAATAAGACTTTACCAATTTGACATGCAGCAGGAATGATTAGGGTAGGATGCCATGGTGTATCCATGCATGAGGGAGGGTCAGTGATATGGACAGGAGACGGAAATACTGGGTAGAAGAGGGTGGTTTCCCAGCAAAGGCCCCACCCTCAAGCCTGGAGACCTGCAGCTGTAAATGGGGACAAGCATTCCTGTTTTCATTCCCAAAAAGTTGTCTTTTGACCCACCATGCCCCCTTTCTTTTACCCATATAAACCCCA... |
Task1_train_38954 | The following genetic variant occurs on Chromosome 7. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GAGAAAAGGTGCCAGGAGAAAGATGAATTCAATCATCTATTTCTGCCAGGAAGAAAAGCACCAGGAAGGAATCAGATGTACAGTTTGTCCTCTGGGGACCTCTGCCTTGATCCTCAATAAATCTCCTTTTAGATGCCACGTGCAGCAATTCCCACACTTCACAATGCTCTCCATGGCTTCTGTTGGCCTTATGGTCAGCTCTGCCAAGATCTGTATTCTTGGGCAAGACAGAATCCTTCTGAATCTCAGTCTCTTCCTCTATAAATGGAAATAATTTTGCTCCACACAAGTCACCATTAGCACGTTGGTGGGAAGTTAAA... | GAGAAAAGGTGCCAGGAGAAAGATGAATTCAATCATCTATTTCTGCCAGGAAGAAAAGCACCAGGAAGGAATCAGATGTACAGTTTGTCCTCTGGGGACCTCTGCCTTGATCCTCAATAAATCTCCTTTTAGATGCCACGTGCAGCAATTCCCACACTTCACAATGCTCTCCATGGCTTCTGTTGGCCTTATGGTCAGCTCTGCCAAGATCTGTATTCTTGGGCAAGACAGAATCCTTCTGAATCTCAGTCTCTTCCTCTATAAATGGAAATAATTTTGCTCCACACAAGTCACCATTAGCACGTTGGTGGGAAGTTAAA... |
Task1_train_38955 | A mutation located on Chromosome 7 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CTGAGCAGGTGGGCACAGTGAGCCCCACCAGGGAGACCCAGTGACATAGATGGTCTGCTCAGGGTGATGCATGTTCCAAGGAGGGACCTCTCTGCCCCCCACCATTACCATCACTGTGACTTTCCCCAAGCCCTTCCCATTTTAATTCACTGCCTTTGTCTTTTCCAAGCCCCACACAGTCAGACTAACCTCTGCCACCTGCGCTTCCTGCCGCTGCCCAGTGGTTGGGGGAGGGGGACTAGCAGGGAGGAAACATTTTTGTATCATGGTGTAACATTGTGGGGACTAGCGGGAGGGCACGATGATTCAGGTAGAGGAGG... | CTGAGCAGGTGGGCACAGTGAGCCCCACCAGGGAGACCCAGTGACATAGATGGTCTGCTCAGGGTGATGCATGTTCCAAGGAGGGACCTCTCTGCCCCCCACCATTACCATCACTGTGACTTTCCCCAAGCCCTTCCCATTTTAATTCACTGCCTTTGTCTTTTCCAAGCCCCACACAGTCAGACTAACCTCTGCCACCTGCGCTTCCTGCCGCTGCCCAGTGGTTGGGGGAGGGGGACTAGCAGGGAGGAAACATTTTTGTATCATGGTGTAACATTGTGGGGACTAGCGGGAGGGCACGATGATTCAGGTAGAGGAGG... |
Task1_train_38956 | Here is a variant on Chromosome 7. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CAGAATCAGCATCTGAATAGGCACAGCATAGGGTTCAAGTTTCATGGTTTTGCCATCCAAGCATGTTTAGCATTTTAAATATTAATATTTATTACATACTTGTAGTTTATGATTTGAAATTTTTTAACTAAGTCTTCCTCTTGGGTAAGTTGTAATGAAAATAATCTTGTAAGCTTAAGGAGCGGAAAATAATACCTGTTGAAAATTAGAGCTTGTAATAGGGCTTTATAAACACCATCTCATTTAATACACATAACAATTCAATGAGGCAAGTTTTATAGGTGGGGAAAAACTTGAAACTTAGTAAAATTAAATAACTA... | CAGAATCAGCATCTGAATAGGCACAGCATAGGGTTCAAGTTTCATGGTTTTGCCATCCAAGCATGTTTAGCATTTTAAATATTAATATTTATTACATACTTGTAGTTTATGATTTGAAATTTTTTAACTAAGTCTTCCTCTTGGGTAAGTTGTAATGAAAATAATCTTGTAAGCTTAAGGAGCGGAAAATAATACCTGTTGAAAATTAGAGCTTGTAATAGGGCTTTATAAACACCATCTCATTTAATACACATAACAATTCAATGAGGCAAGTTTTATAGGTGGGGAAAAACTTGAAACTTAGTAAAATTAAATAACTA... |
Task1_train_38957 | Chromosome 7 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TGCTTTTGACTTTACCCCTCAGGGCCCAAGTTGTTTGCTTCGCTGGGCAGCCCCAGAGGTCATTGCACATGGAAAGCATACAACATCCAGTGATGTCTGGAGCTTTGGGATACTCATGTGGGAAGTGATGAGTTATGGAGAACGGCCTTACTGGGACATGAGTGAGCAGGAGGTGAGCACTGACCTAGACACTGCTGATTTCCCACCCCGATCCCTCCCAGGTTGGAACATTCTAGGACCTCCATTCTCTACTCCGTTTGTATTCTAAGATCTCATGGCTGTTGGATTGCCATATCTTTGAGTTCCTTCTCCACTCCAAC... | TGCTTTTGACTTTACCCCTCAGGGCCCAAGTTGTTTGCTTCGCTGGGCAGCCCCAGAGGTCATTGCACATGGAAAGCATACAACATCCAGTGATGTCTGGAGCTTTGGGATACTCATGTGGGAAGTGATGAGTTATGGAGAACGGCCTTACTGGGACATGAGTGAGCAGGAGGTGAGCACTGACCTAGACACTGCTGATTTCCCACCCCGATCCCTCCCAGGTTGGAACATTCTAGGACCTCCATTCTCTACTCCGTTTGTATTCTAAGATCTCATGGCTGTTGGATTGCCATATCTTTGAGTTCCTTCTCCACTCCAAC... |
Task1_train_38958 | Here is a variant on Chromosome 7. Please identify whether it is a benign mutation or associated with a disorder. | Benign | ATCAAGAAGACTTGATACTCCAGTTTTTATTTGGGAACAAAATGTACTGAGTGCAATTTTAGCCAACGTTAATTTTCTTTTGATTTATTTCTTGTTGATTCCTCTAGAAAACACTGAGCTTTTAACTGTTGAGAAAACTGTGAGGCATTCTTCTCAGCGATTCCAGTATTGCCTGGTTGAATTGCTAATCAGTGCTTCTGTACATTTTGCATGATTTTGCTAGCTTTGCCACAACTGTCCAAACATAAGTGGGGTGGAGATATCCTGTCTCTCAGCTTGGCAGGTTCCTTGGTAGGAAGGGGATGACTTGCCCTAACCCT... | ATCAAGAAGACTTGATACTCCAGTTTTTATTTGGGAACAAAATGTACTGAGTGCAATTTTAGCCAACGTTAATTTTCTTTTGATTTATTTCTTGTTGATTCCTCTAGAAAACACTGAGCTTTTAACTGTTGAGAAAACTGTGAGGCATTCTTCTCAGCGATTCCAGTATTGCCTGGTTGAATTGCTAATCAGTGCTTCTGTACATTTTGCATGATTTTGCTAGCTTTGCCACAACTGTCCAAACATAAGTGGGGTGGAGATATCCTGTCTCTCAGCTTGGCAGGTTCCTTGGTAGGAAGGGGATGACTTGCCCTAACCCT... |
Task1_train_38959 | With a mutation on Chromosome 7, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | GTCACCAGCTCCCCGACCAGCCGGATATCGTCCTTAGGGGTCATGTAGGCTTCCTAATGGGGGAGAAGAACAGTCAAAATGCTCAGGGCTTTCAGGCCTCTGCCCTGCATTTCCATGGTGCCCAGGGTCACCAGTCTTAGCAGATTCTTTTTAATCTGTTAGGTTTGGGTCTTCTCAAACTCTGCTCTCAGAGTAAGAGCGTATGTGTGTTTTTGTGGGCGTGCATTTGGAGTTTGTACCCATATATTTGAGATTAGAGCAAGGGGAGAAATGGTGTGAGGGAGGAAAGGGACACCAGTCTCTGAGGACAGAGAGCCAAG... | GTCACCAGCTCCCCGACCAGCCGGATATCGTCCTTAGGGGTCATGTAGGCTTCCTAATGGGGGAGAAGAACAGTCAAAATGCTCAGGGCTTTCAGGCCTCTGCCCTGCATTTCCATGGTGCCCAGGGTCACCAGTCTTAGCAGATTCTTTTTAATCTGTTAGGTTTGGGTCTTCTCAAACTCTGCTCTCAGAGTAAGAGCGTATGTGTGTTTTTGTGGGCGTGCATTTGGAGTTTGTACCCATATATTTGAGATTAGAGCAAGGGGAGAAATGGTGTGAGGGAGGAAAGGGACACCAGTCTCTGAGGACAGAGAGCCAAG... |
Task1_train_38960 | This alteration occurs on Chromosome 7. Is it associated with a disease or is it a benign variant? | Benign | GGGAGGCTGAGACAGGAGAATCACTTGAACCCAGGAGGTGGAGGTTGTAGGTGAGCTGAGATCGTGCCATTGCCCTCCCGTCTGGGCAACAAGAGTGAGACTCCATCTCAAAAAAAAAAAAGTGATTATCACTGGATGGTGGAATTATTAGCCTTTTTGGGGTTTTGTATTTTTCTATATTTTCTACTTTGTAATAAGAAAAAATATTTAAGGGATTCCCTGTTTTCTGCAAGAATTTATCTCTTTTAACACTGCGGAGGTCAGGCGGGTGGTGGTGGCAAGGAAATGGAAGTAATGGAAACAACTCAGTTATTTCCACT... | GGGAGGCTGAGACAGGAGAATCACTTGAACCCAGGAGGTGGAGGTTGTAGGTGAGCTGAGATCGTGCCATTGCCCTCCCGTCTGGGCAACAAGAGTGAGACTCCATCTCAAAAAAAAAAAAGTGATTATCACTGGATGGTGGAATTATTAGCCTTTTTGGGGTTTTGTATTTTTCTATATTTTCTACTTTGTAATAAGAAAAAATATTTAAGGGATTCCCTGTTTTCTGCAAGAATTTATCTCTTTTAACACTGCGGAGGTCAGGCGGGTGGTGGTGGCAAGGAAATGGAAGTAATGGAAACAACTCAGTTATTTCCACT... |
Task1_train_38961 | Here is a variant on Chromosome 7. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TTTGTATTTTTCTATATTTTCTACTTTGTAATAAGAAAAAATATTTAAGGGATTCCCTGTTTTCTGCAAGAATTTATCTCTTTTAACACTGCGGAGGTCAGGCGGGTGGTGGTGGCAAGGAAATGGAAGTAATGGAAACAACTCAGTTATTTCCACTCAAGCCTGCCCGGGAGGCAATTCTCACCCCAGCCGCCCTCCCCATTCATTCCCACAGAGCTGGAGATGGCTTCTCTTTTTGCCAGGAAACCAAGAGGCTGCTCCCCCAAAATAGCCAGGAGGGAGGAGATTAGTGATGGTTTTTTCCATTCAAGCATCATTCT... | TTTGTATTTTTCTATATTTTCTACTTTGTAATAAGAAAAAATATTTAAGGGATTCCCTGTTTTCTGCAAGAATTTATCTCTTTTAACACTGCGGAGGTCAGGCGGGTGGTGGTGGCAAGGAAATGGAAGTAATGGAAACAACTCAGTTATTTCCACTCAAGCCTGCCCGGGAGGCAATTCTCACCCCAGCCGCCCTCCCCATTCATTCCCACAGAGCTGGAGATGGCTTCTCTTTTTGCCAGGAAACCAAGAGGCTGCTCCCCCAAAATAGCCAGGAGGGAGGAGATTAGTGATGGTTTTTTCCATTCAAGCATCATTCT... |
Task1_train_38962 | Located on Chromosome 7, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TTTGTTTGTGTTTGAAATGTTTTAAAGTACCCTTTTAGTGAACTGAAATTCCAAGAAACAGTGTAAAGCTGTAAAGATCTTCACACACACACATGCTGGCAATGAGAAGAAGTGTAGAGAGATGATGGGCAAAAAAAATTTGAGTTCTATTGACGGTCTAACAATAAGAACAGTGATAACAATAACAACAACGATTTGTTGGCTAGTATGTGCTAGTCACTGCACTAAGTAGTTTACTTATTTAATTTTATAATCACCATAGAGGCTAAGTACCAGTAATACCATTATTTTACAGCTGAATAAACGGGCTCAGAGAGAGT... | TTTGTTTGTGTTTGAAATGTTTTAAAGTACCCTTTTAGTGAACTGAAATTCCAAGAAACAGTGTAAAGCTGTAAAGATCTTCACACACACACATGCTGGCAATGAGAAGAAGTGTAGAGAGATGATGGGCAAAAAAAATTTGAGTTCTATTGACGGTCTAACAATAAGAACAGTGATAACAATAACAACAACGATTTGTTGGCTAGTATGTGCTAGTCACTGCACTAAGTAGTTTACTTATTTAATTTTATAATCACCATAGAGGCTAAGTACCAGTAATACCATTATTTTACAGCTGAATAAACGGGCTCAGAGAGAGT... |
Task1_train_38963 | A mutation is present on Chromosome 7. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | AGTGAGGTTTAGACTCATATTTATTTATTTTAGAATTAGAATAGAATATACCTACAATCGTATATTTGAATATAAAGATTGCATAATCCTTTAAAGCTGAAGGAAACTTGTGGCAAAAACAATGCTTAAACATTTTTGTGCTACAGGCCATTTCGTTGGTTTCATGAAGTTTATGAAACATTTATCAGAAAATTGCTTCTAAATGTATAAAGTGCATTGGATTACAGAGAGAAACTACCACATTGAGTAACAGTGACTAACTTGTAAAAAATAAATTTGTGATGCAGTAAGGTATGTGTTTCTTTATGCACACATTAGCT... | AGTGAGGTTTAGACTCATATTTATTTATTTTAGAATTAGAATAGAATATACCTACAATCGTATATTTGAATATAAAGATTGCATAATCCTTTAAAGCTGAAGGAAACTTGTGGCAAAAACAATGCTTAAACATTTTTGTGCTACAGGCCATTTCGTTGGTTTCATGAAGTTTATGAAACATTTATCAGAAAATTGCTTCTAAATGTATAAAGTGCATTGGATTACAGAGAGAAACTACCACATTGAGTAACAGTGACTAACTTGTAAAAAATAAATTTGTGATGCAGTAAGGTATGTGTTTCTTTATGCACACATTAGCT... |
Task1_train_38964 | A change on Chromosome 7 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TGTAGTCCCAGCTACTCAGGTGGCTGAAGTGTGGGGATCACCTGAGCTATGGAGGTCAAGGCTGCAGTGAGCCATGATTACACCACTGCACTCCAGCCTGGGTGATAGAGTGAGACCCAGTCTCAAAAAGAAAAATAATCAAATAAAAATAACAGGGTAAGCACACTGGAAAATGATAACTGGCACTCAGCTTCTGTGTCAAGAAGACACTAGGAATTAGTATTGTCAACAAACTGAAAAGTATATACCTTGTTTAAAATGGGCAGCCATTACTCAGCTTCAGCCAGTTCACTATGAAGACCCAATACTGCCAAATCTTC... | TGTAGTCCCAGCTACTCAGGTGGCTGAAGTGTGGGGATCACCTGAGCTATGGAGGTCAAGGCTGCAGTGAGCCATGATTACACCACTGCACTCCAGCCTGGGTGATAGAGTGAGACCCAGTCTCAAAAAGAAAAATAATCAAATAAAAATAACAGGGTAAGCACACTGGAAAATGATAACTGGCACTCAGCTTCTGTGTCAAGAAGACACTAGGAATTAGTATTGTCAACAAACTGAAAAGTATATACCTTGTTTAAAATGGGCAGCCATTACTCAGCTTCAGCCAGTTCACTATGAAGACCCAATACTGCCAAATCTTC... |
Task1_train_38965 | This alteration on Chromosome 7 may affect genome function. Does it lead to a disease or is it benign? | Benign | CTACTAGGAAGCTCATGTGGAGAAATAGAATTATAGCTAGAGAAGTAAATATGATTTCATGTTTTATTCTTGTGTCTTAGGCCAAAGTGGGCAGTTTCAGCCAGAATGTGGAACTCCTCAACTTGCTGCCTAAGAGGGGTCCCCAAGCTTTTGATGCCTTCTGTGAAGCACTGAGGGAGACCAAGCAAGGCCACCTGGAGGATATGTTGCTCACCACCCTTTCTGGGCTTCAGCATGTACTCCCACCGGTATGAAGCTTTAGTAATATGGGGTGTTGGGAAGGGTTAGTTTGACTGGAAAGGAATTTGTAAGTCAGAGTG... | CTACTAGGAAGCTCATGTGGAGAAATAGAATTATAGCTAGAGAAGTAAATATGATTTCATGTTTTATTCTTGTGTCTTAGGCCAAAGTGGGCAGTTTCAGCCAGAATGTGGAACTCCTCAACTTGCTGCCTAAGAGGGGTCCCCAAGCTTTTGATGCCTTCTGTGAAGCACTGAGGGAGACCAAGCAAGGCCACCTGGAGGATATGTTGCTCACCACCCTTTCTGGGCTTCAGCATGTACTCCCACCGGTATGAAGCTTTAGTAATATGGGGTGTTGGGAAGGGTTAGTTTGACTGGAAAGGAATTTGTAAGTCAGAGTG... |
Task1_train_38966 | An alteration has been detected on Chromosome 7. Is it pathogenic, and if so, what disease is involved? | Benign | CAAAGTGCTGGGATTACAGGCATGAGCCACTGTGCCCGGCTGGAACTGTTTCACATGGAGGAGTGAATGGTTGTTAGTAAACGATAATTTCACATTTCTCTGCCTTCACCATCATTTGACACTTCATCCTGCTTTGTATGATTTCTTATTGTGGTTTATATATCTATATCTTGTCTTCCTAACTAGGTGGGCATTCCTTGAGAATAGAGGCTATGAATTCTATATACCCAGAGTGCCTTGTTATAGGTATCTACTAGATATTAAATGAATAATTTCCTAGTGTTTGAATTAGTGTAATAAAGAAAAATCATGTAGGGCCA... | CAAAGTGCTGGGATTACAGGCATGAGCCACTGTGCCCGGCTGGAACTGTTTCACATGGAGGAGTGAATGGTTGTTAGTAAACGATAATTTCACATTTCTCTGCCTTCACCATCATTTGACACTTCATCCTGCTTTGTATGATTTCTTATTGTGGTTTATATATCTATATCTTGTCTTCCTAACTAGGTGGGCATTCCTTGAGAATAGAGGCTATGAATTCTATATACCCAGAGTGCCTTGTTATAGGTATCTACTAGATATTAAATGAATAATTTCCTAGTGTTTGAATTAGTGTAATAAAGAAAAATCATGTAGGGCCA... |
Task1_train_38967 | This variant is located on Chromosome 7. Evaluate its biological effect and specify any disease association. | Benign | GGGCATGCTAGACCACCTCTCAGAGCTCCTGGAAATGAGGTCCTGGGACATGGAGTCAGCACACGTTAGCAAGCACAAGAGGACTCTTCCCCTGTACAGGCAGCATTCGGTTAGGTGACTGCACCTGCCTTGGTTCACCTTGCCTACGCCCATGTTTCCTCCAAAAACCAACCTCAGGATAACCATTGTCCCCCTTCCATGGAAGACACAGAACCCCCTGCCCTGCTTGCATCCCAGAAGTGTGAGTAAGAGAGTATGAACTTGATGGCGGGACAGGACCATAGATGGACAGAAACACCCCAACTCTCAACCTTCTCACT... | GGGCATGCTAGACCACCTCTCAGAGCTCCTGGAAATGAGGTCCTGGGACATGGAGTCAGCACACGTTAGCAAGCACAAGAGGACTCTTCCCCTGTACAGGCAGCATTCGGTTAGGTGACTGCACCTGCCTTGGTTCACCTTGCCTACGCCCATGTTTCCTCCAAAAACCAACCTCAGGATAACCATTGTCCCCCTTCCATGGAAGACACAGAACCCCCTGCCCTGCTTGCATCCCAGAAGTGTGAGTAAGAGAGTATGAACTTGATGGCGGGACAGGACCATAGATGGACAGAAACACCCCAACTCTCAACCTTCTCACT... |
Task1_train_38968 | This variant is present on Chromosome 7. Is the change likely to result in a pathogenic outcome? | Benign | TGGTGAGCTTCCTTCACCTGGAGATGCAGGGCAGAGAAGTCTGCTTCCTTGCTGCCCAACCTGGCTTATGCGTGCGCACACCGGGGATGAAAGCCCTGGCTAACTCGGCTGGCCCTTTCTGCCCCTTCCAGGCAGTACGCCCCGAGGTGCTCCGTCTGCTCTGAGCCCATCATGCCTGAGCCTGGCCGAGATGAGACTGTGCGAGTGGTCGCCCTGGACAAGAACTTCCACATGAAGTGTTACAAGTGTGAGGTCAGCCATCCCTCTGGACTCCTTGGGCAGGTTCTGACCAGGAGGTGGCGGGAGATGCTGCTTACTAA... | TGGTGAGCTTCCTTCACCTGGAGATGCAGGGCAGAGAAGTCTGCTTCCTTGCTGCCCAACCTGGCTTATGCGTGCGCACACCGGGGATGAAAGCCCTGGCTAACTCGGCTGGCCCTTTCTGCCCCTTCCAGGCAGTACGCCCCGAGGTGCTCCGTCTGCTCTGAGCCCATCATGCCTGAGCCTGGCCGAGATGAGACTGTGCGAGTGGTCGCCCTGGACAAGAACTTCCACATGAAGTGTTACAAGTGTGAGGTCAGCCATCCCTCTGGACTCCTTGGGCAGGTTCTGACCAGGAGGTGGCGGGAGATGCTGCTTACTAA... |
Task1_train_38969 | This mutation occurs on Chromosome 7. Does this change lead to a known medical condition, or is it benign? | Benign | GATTTCTCAGAAAATTAAAAACAGACCTACCTTATCCAGTAATTCCACTTTTAGGTGTATATGCAAAGGAAATGAAACTAGTATTTTGAAGAGATATCTGCACTCCCATGTTCATTGAAAATTATTCACAATAGCCAAGACATGGAAACAATCTAAAAGCCCATTAACAGATGAATGAACAAAGAAAATGTGGTGTGCATACACAATGGAATATGATTCAGTCTTAGAAAAGGCGATTCTGCCATTTGCAACAACGTAGATGGAACTGGAGGACATTATGCTATGTGAAATGCTCCAGAGACAGAAATACATATATTGTA... | GATTTCTCAGAAAATTAAAAACAGACCTACCTTATCCAGTAATTCCACTTTTAGGTGTATATGCAAAGGAAATGAAACTAGTATTTTGAAGAGATATCTGCACTCCCATGTTCATTGAAAATTATTCACAATAGCCAAGACATGGAAACAATCTAAAAGCCCATTAACAGATGAATGAACAAAGAAAATGTGGTGTGCATACACAATGGAATATGATTCAGTCTTAGAAAAGGCGATTCTGCCATTTGCAACAACGTAGATGGAACTGGAGGACATTATGCTATGTGAAATGCTCCAGAGACAGAAATACATATATTGTA... |
Task1_train_38970 | A mutation is present on Chromosome 7. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CTCCTTAATACACATAATCACATGCTTTGCTTTTTTCATTTAACAACTTTTATGAGACCTGGTTCCACACCTGCCATAGATAAAACTGTTTCATTCTTCTCAGCAGCTGCATAGAATTCCATCACAGGGATAAACCAAAATGCATTTAATTGGTCACATATTGATTGATATTTAAGAAATTACTAGATTTTTGATAATCCAAGTAACGCTGACATGAATATTTTTGAACATTCATATTTTCCCACAAAGCAAATAAATTTGTAGGGTCAAACCCTGGAAGTACATTGAAACAAATAATACATGCCATTTATTTTAATTAA... | CTCCTTAATACACATAATCACATGCTTTGCTTTTTTCATTTAACAACTTTTATGAGACCTGGTTCCACACCTGCCATAGATAAAACTGTTTCATTCTTCTCAGCAGCTGCATAGAATTCCATCACAGGGATAAACCAAAATGCATTTAATTGGTCACATATTGATTGATATTTAAGAAATTACTAGATTTTTGATAATCCAAGTAACGCTGACATGAATATTTTTGAACATTCATATTTTCCCACAAAGCAAATAAATTTGTAGGGTCAAACCCTGGAAGTACATTGAAACAAATAATACATGCCATTTATTTTAATTAA... |
Task1_train_38971 | A mutation found on Chromosome 7 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TAAAACTGTTTCATTCTTCTCAGCAGCTGCATAGAATTCCATCACAGGGATAAACCAAAATGCATTTAATTGGTCACATATTGATTGATATTTAAGAAATTACTAGATTTTTGATAATCCAAGTAACGCTGACATGAATATTTTTGAACATTCATATTTTCCCACAAAGCAAATAAATTTGTAGGGTCAAACCCTGGAAGTACATTGAAACAAATAATACATGCCATTTATTTTAATTAATATCATCCACTTTCCCTGTATAGAAATTGTATACATTTATACTCTCATTAATAACATACAAGAGAGCCTGTTTCACCTTC... | TAAAACTGTTTCATTCTTCTCAGCAGCTGCATAGAATTCCATCACAGGGATAAACCAAAATGCATTTAATTGGTCACATATTGATTGATATTTAAGAAATTACTAGATTTTTGATAATCCAAGTAACGCTGACATGAATATTTTTGAACATTCATATTTTCCCACAAAGCAAATAAATTTGTAGGGTCAAACCCTGGAAGTACATTGAAACAAATAATACATGCCATTTATTTTAATTAATATCATCCACTTTCCCTGTATAGAAATTGTATACATTTATACTCTCATTAATAACATACAAGAGAGCCTGTTTCACCTTC... |
Task1_train_38972 | A variant has been detected on Chromosome 7. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TCTCTTTTCTCTTTTTGGTTTGCTTAAAGCGGCATCCCATGGAGAAAGCTTTGGGTTATTTTTTACATAATAAATTTCATGTTTTGTGTTATGCTTAGAAAGTCAGTTCATTTTTTTAATGTTAATGCTCCTTGTCTTATCTTGAAGCTGCTCTTCTAACTGCACTTGCTCATTCTGGGAGATCTCGGCCATGCAAATCTCAGATATGCTGGTGACTTCTACCAGCTATGCCAGTTTTTAACATGCTGGTGACTTCTACCAGCCATGCCAATCTCTAACATGCTGGTGAATTCTATCAGCCATGCCAGTCTCTAACATCG... | TCTCTTTTCTCTTTTTGGTTTGCTTAAAGCGGCATCCCATGGAGAAAGCTTTGGGTTATTTTTTACATAATAAATTTCATGTTTTGTGTTATGCTTAGAAAGTCAGTTCATTTTTTTAATGTTAATGCTCCTTGTCTTATCTTGAAGCTGCTCTTCTAACTGCACTTGCTCATTCTGGGAGATCTCGGCCATGCAAATCTCAGATATGCTGGTGACTTCTACCAGCTATGCCAGTTTTTAACATGCTGGTGACTTCTACCAGCCATGCCAATCTCTAACATGCTGGTGAATTCTATCAGCCATGCCAGTCTCTAACATCG... |
Task1_train_38973 | This variant is located on Chromosome 7. Evaluate its biological effect and specify any disease association. | Benign | AAACGCTTCACAAAATTTTGTGTAATCTATATGCAGGAGACGTGTTAATCTTGTCTGTGTCATTCTAATTTTAGAAAGTGCTGCCAAAGCCAACACTCCTTGCTGATTTTCTGTCTAGTTCTATCCATTATTGAAAAACGCAAGAGAAAATTTCCAACTATAATTGTGGATTCATCTATACCTACTTTCAGTTCTGGCAGTTTTCTTTTTAAAAAAAAAATCAACTAAAGTTTATTAAATTAAGCATAAAGTTACTTTCACATTTATCTACAACCACAGTGAATACAGTTCTTGGCATGAAGACACCACAACCTTTAGAA... | AAACGCTTCACAAAATTTTGTGTAATCTATATGCAGGAGACGTGTTAATCTTGTCTGTGTCATTCTAATTTTAGAAAGTGCTGCCAAAGCCAACACTCCTTGCTGATTTTCTGTCTAGTTCTATCCATTATTGAAAAACGCAAGAGAAAATTTCCAACTATAATTGTGGATTCATCTATACCTACTTTCAGTTCTGGCAGTTTTCTTTTTAAAAAAAAAATCAACTAAAGTTTATTAAATTAAGCATAAAGTTACTTTCACATTTATCTACAACCACAGTGAATACAGTTCTTGGCATGAAGACACCACAACCTTTAGAA... |
Task1_train_38974 | A mutation on Chromosome 7 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CCCCATAAATCTCCATTTCTTTAGGGTCCATTATTAGCCCTTTATTAGTTTCTTTTGGAGGTGTCATAACTCCCCAGTGCTTTGTAATCCTTGTGTCTTTGCATTGTTATCTTTTCATTTGAAGAGATACCCCCTCCTTCTGGCCTTTACAGGTGTTCTTTGGCAGGGCTAGACCTATACTATTTAGTGTAGCCTGTAATTCTTCAAGGGCCAGCTGGTAATGGCCCTGGGCAAGCAAAGCTAACTGTGGATTTTCTACCTGCCTGGGATGCTGTCTTTGCTCTGATATTGGCTGGGGCTATTGACTGGGCCCTGCTGTC... | CCCCATAAATCTCCATTTCTTTAGGGTCCATTATTAGCCCTTTATTAGTTTCTTTTGGAGGTGTCATAACTCCCCAGTGCTTTGTAATCCTTGTGTCTTTGCATTGTTATCTTTTCATTTGAAGAGATACCCCCTCCTTCTGGCCTTTACAGGTGTTCTTTGGCAGGGCTAGACCTATACTATTTAGTGTAGCCTGTAATTCTTCAAGGGCCAGCTGGTAATGGCCCTGGGCAAGCAAAGCTAACTGTGGATTTTCTACCTGCCTGGGATGCTGTCTTTGCTCTGATATTGGCTGGGGCTATTGACTGGGCCCTGCTGTC... |
Task1_train_38975 | A variant on Chromosome 7 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TGGTAATGGCCCTGGGCAAGCAAAGCTAACTGTGGATTTTCTACCTGCCTGGGATGCTGTCTTTGCTCTGATATTGGCTGGGGCTATTGACTGGGCCCTGCTGTCTGGCAAGACCACTGGCTGAGCTCTGTTATCACACAGAGCTACTGACTGCGTACTGCAATGGCTTCTGGTCAGACTAGTCACAGAATTTATTCCCTGGCTGGAAAATTATGCTTTCTGGGATTTGCAGTTGGGCAGGGCTGTAGGCTGAACTCCAAAGTTAGGAGAAGTTGCTGCTTAGAATGATTGAGGCCAGAGGCTACACTCAGAAAAACACA... | TGGTAATGGCCCTGGGCAAGCAAAGCTAACTGTGGATTTTCTACCTGCCTGGGATGCTGTCTTTGCTCTGATATTGGCTGGGGCTATTGACTGGGCCCTGCTGTCTGGCAAGACCACTGGCTGAGCTCTGTTATCACACAGAGCTACTGACTGCGTACTGCAATGGCTTCTGGTCAGACTAGTCACAGAATTTATTCCCTGGCTGGAAAATTATGCTTTCTGGGATTTGCAGTTGGGCAGGGCTGTAGGCTGAACTCCAAAGTTAGGAGAAGTTGCTGCTTAGAATGATTGAGGCCAGAGGCTACACTCAGAAAAACACA... |
Task1_train_38976 | This mutation is located on Chromosome 7. Is it associated with a disease or is it a benign polymorphism? | Benign | ATGGTTGCTTCCCTGTTAAGGTGGAGCTTCCTTGTAGGGTTTCTTCCCTTTAAGATGGGCTTTTGGCTGAATTGAGTTTGACTTCCCAGGTCAAACAGTTCTAGCCCTCATGCTTCTCTGAAAGGCATGTAGATGTCCTTGATGGGGCCTTTTAGCTGAGTAGAGCCATGGATTGACTTCCTGGGTTAAGCAGGTCTACCTCATGTGTGTTTCTGAAATGGGTGGAGGTGTGTATCTCCTTGTCTTGGCAGAGGTCACTGGTGTGGGCTCTGAGACTGGACATGGGGACTAGCTATCTAAGGCCTCAAGCTAGGTTGTAC... | ATGGTTGCTTCCCTGTTAAGGTGGAGCTTCCTTGTAGGGTTTCTTCCCTTTAAGATGGGCTTTTGGCTGAATTGAGTTTGACTTCCCAGGTCAAACAGTTCTAGCCCTCATGCTTCTCTGAAAGGCATGTAGATGTCCTTGATGGGGCCTTTTAGCTGAGTAGAGCCATGGATTGACTTCCTGGGTTAAGCAGGTCTACCTCATGTGTGTTTCTGAAATGGGTGGAGGTGTGTATCTCCTTGTCTTGGCAGAGGTCACTGGTGTGGGCTCTGAGACTGGACATGGGGACTAGCTATCTAAGGCCTCAAGCTAGGTTGTAC... |
Task1_train_38977 | This genomic variant is located on Chromosome 7. Can you determine its pathogenicity and name any linked disease? | Benign | GAATTTGAATTTGAATGTCTCTTTGAGGAAATCAAACGTATTCTCAGCCTCATTATGATTTTAGAAAAGCACCCTGAGGGGTGCTGGTGGGAGCATCAGGACAGAGCAGTAAAGGAGGAAATGTTGGAGAAGGAAGGTCTTGAGGAGGACATTAGGGAGAGTTTAGAAAAAATGGTTGTGAACTATGAAAGGGATGAGTATTTCTGGAACTACATGTTTTGCTTAATCCTTTATCACATAAGAGAGTTGAAGTATTGACAGTCTTTCCCTTGCGAGTAAGAGACCCTAGTCTGTCTGGACCTGTTTCTGTCCTTAATGCC... | GAATTTGAATTTGAATGTCTCTTTGAGGAAATCAAACGTATTCTCAGCCTCATTATGATTTTAGAAAAGCACCCTGAGGGGTGCTGGTGGGAGCATCAGGACAGAGCAGTAAAGGAGGAAATGTTGGAGAAGGAAGGTCTTGAGGAGGACATTAGGGAGAGTTTAGAAAAAATGGTTGTGAACTATGAAAGGGATGAGTATTTCTGGAACTACATGTTTTGCTTAATCCTTTATCACATAAGAGAGTTGAAGTATTGACAGTCTTTCCCTTGCGAGTAAGAGACCCTAGTCTGTCTGGACCTGTTTCTGTCCTTAATGCC... |
Task1_train_38978 | Here is a variant on Chromosome 7. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GCCTCATTATGATTTTAGAAAAGCACCCTGAGGGGTGCTGGTGGGAGCATCAGGACAGAGCAGTAAAGGAGGAAATGTTGGAGAAGGAAGGTCTTGAGGAGGACATTAGGGAGAGTTTAGAAAAAATGGTTGTGAACTATGAAAGGGATGAGTATTTCTGGAACTACATGTTTTGCTTAATCCTTTATCACATAAGAGAGTTGAAGTATTGACAGTCTTTCCCTTGCGAGTAAGAGACCCTAGTCTGTCTGGACCTGTTTCTGTCCTTAATGCCTCCTGCCTCATTTGTTTCCTACTTTCCCTTATTGTGAACACTGCAA... | GCCTCATTATGATTTTAGAAAAGCACCCTGAGGGGTGCTGGTGGGAGCATCAGGACAGAGCAGTAAAGGAGGAAATGTTGGAGAAGGAAGGTCTTGAGGAGGACATTAGGGAGAGTTTAGAAAAAATGGTTGTGAACTATGAAAGGGATGAGTATTTCTGGAACTACATGTTTTGCTTAATCCTTTATCACATAAGAGAGTTGAAGTATTGACAGTCTTTCCCTTGCGAGTAAGAGACCCTAGTCTGTCTGGACCTGTTTCTGTCCTTAATGCCTCCTGCCTCATTTGTTTCCTACTTTCCCTTATTGTGAACACTGCAA... |
Task1_train_38979 | A mutation found on Chromosome 7 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AAGATAGTAAGATAGTTAGTAAATGATGCCATCTAACTACCTTAGTAAATGGCATCACCTCTAGGTAATAAGCTCTATATTTGGGGTTCCTCCGTGATTTCTTTCTTTCTCTCACCTTCCATATCCAAGTCACCAATTACTGTTAAAGATTCTGCTTCTAACGTGTATCTTAAATCTGCTTCTCTGGAACCACAGTATTTAAGTTCACTGTCACCTATTCTGAGTAGCCTCCAACTAGTTTCATAGCTCACAGCTCATGCTCTTGCCTCCAAGGAGTCCGTTTTGCAACGACAGAGTTATCTTTCCATTGCGTAAATCAT... | AAGATAGTAAGATAGTTAGTAAATGATGCCATCTAACTACCTTAGTAAATGGCATCACCTCTAGGTAATAAGCTCTATATTTGGGGTTCCTCCGTGATTTCTTTCTTTCTCTCACCTTCCATATCCAAGTCACCAATTACTGTTAAAGATTCTGCTTCTAACGTGTATCTTAAATCTGCTTCTCTGGAACCACAGTATTTAAGTTCACTGTCACCTATTCTGAGTAGCCTCCAACTAGTTTCATAGCTCACAGCTCATGCTCTTGCCTCCAAGGAGTCCGTTTTGCAACGACAGAGTTATCTTTCCATTGCGTAAATCAT... |
Task1_train_38980 | Here is a variant on Chromosome 7. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CCTGCCAGCTTTTTTTTTTCTGAATGCCCATCCCCAGGGCCCAGAGAAATGGAGACAGGAGGATAAACTACTTTTGTTTGTTCTGGTAGACACAGAGTCTGACTGCTGTGTATCCTGTTTCCCTTAGGGACTCTACCTTGTCCTCAGGGACAATCCGTGAAGGCTTGAGTGGAGATAACCCCACCATAAAACCTATACTGCTGGTGTTCCCAGAGAGCAGGCTGCAGTCTGCATCAGCCTATGCTAAGAAAAGAGAGACAACTCCTGCATCTGGAAATTCCTTCTCTCAGGGGCTGCTGGTGGGAGCAAGATCCTCAGCT... | CCTGCCAGCTTTTTTTTTTCTGAATGCCCATCCCCAGGGCCCAGAGAAATGGAGACAGGAGGATAAACTACTTTTGTTTGTTCTGGTAGACACAGAGTCTGACTGCTGTGTATCCTGTTTCCCTTAGGGACTCTACCTTGTCCTCAGGGACAATCCGTGAAGGCTTGAGTGGAGATAACCCCACCATAAAACCTATACTGCTGGTGTTCCCAGAGAGCAGGCTGCAGTCTGCATCAGCCTATGCTAAGAAAAGAGAGACAACTCCTGCATCTGGAAATTCCTTCTCTCAGGGGCTGCTGGTGGGAGCAAGATCCTCAGCT... |
Task1_train_38981 | A variant was discovered on Chromosome 7. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CTGCATCAGCCTATGCTAAGAAAAGAGAGACAACTCCTGCATCTGGAAATTCCTTCTCTCAGGGGCTGCTGGTGGGAGCAAGATCCTCAGCTCTGGCCTTCAAAAGCTCCTGTGATCTCTGCACAATTTCTCTAAATAGAATTATATTTCTGAGACAAGACCAGGCCTGATACCACAGTGAGTAAAGGGTCTTTTGCAAAGTCTGGTAGTTTAGAGAAGCTAGGGTCTGGATGAAGGCAGGGCTCCAGAAATCAGTACATTGAATGGGAGATACAGAGGTAATTTATTGGCAGACAGTTTCCTGGGCTAAAGGTGGAGTT... | CTGCATCAGCCTATGCTAAGAAAAGAGAGACAACTCCTGCATCTGGAAATTCCTTCTCTCAGGGGCTGCTGGTGGGAGCAAGATCCTCAGCTCTGGCCTTCAAAAGCTCCTGTGATCTCTGCACAATTTCTCTAAATAGAATTATATTTCTGAGACAAGACCAGGCCTGATACCACAGTGAGTAAAGGGTCTTTTGCAAAGTCTGGTAGTTTAGAGAAGCTAGGGTCTGGATGAAGGCAGGGCTCCAGAAATCAGTACATTGAATGGGAGATACAGAGGTAATTTATTGGCAGACAGTTTCCTGGGCTAAAGGTGGAGTT... |
Task1_train_38982 | The following genetic variant occurs on Chromosome 7. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | ACCAGGCCTGATACCACAGTGAGTAAAGGGTCTTTTGCAAAGTCTGGTAGTTTAGAGAAGCTAGGGTCTGGATGAAGGCAGGGCTCCAGAAATCAGTACATTGAATGGGAGATACAGAGGTAATTTATTGGCAGACAGTTTCCTGGGCTAAAGGTGGAGTTAGCATTTGCAGAGGTGGAGTCATAAGCTGCACATTGAGAATGACGCATTGATCATTTAACATTTGTGTACTTCTATGAAACATCCTGGTTTCCCCTTTCTATAGCCCCTGTGGCTATGTGGTTGGGGGAATGACAAGCAGAGAAAATTTAAGAAGAGTC... | ACCAGGCCTGATACCACAGTGAGTAAAGGGTCTTTTGCAAAGTCTGGTAGTTTAGAGAAGCTAGGGTCTGGATGAAGGCAGGGCTCCAGAAATCAGTACATTGAATGGGAGATACAGAGGTAATTTATTGGCAGACAGTTTCCTGGGCTAAAGGTGGAGTTAGCATTTGCAGAGGTGGAGTCATAAGCTGCACATTGAGAATGACGCATTGATCATTTAACATTTGTGTACTTCTATGAAACATCCTGGTTTCCCCTTTCTATAGCCCCTGTGGCTATGTGGTTGGGGGAATGACAAGCAGAGAAAATTTAAGAAGAGTC... |
Task1_train_38983 | A variant on Chromosome 7 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TATTTGTACATGATAGTTAAGAAGCTATAAAATATGTTAAACATTCTATGAATATAAGTATATGGTTAGAGTTTTAGCTCTAGTTTTGGATAGAGATCAGTATTTTTTAAATCCCAGGCTATGACCCATCATGAAATAATTCAGCCAGCACTTTTACTAATGAAATAGAATACATTAGACTAGAATAAAACAGAAAACAAGCACATTACACAGAGTAAGGATTCAATTGTATATGTACTCATGTGTGTATGTACTGGGTAGACATTTATTACTGTAGGAATATAGCAGAATTTTAGAAATTTCCAAATGCAACTAAATAA... | TATTTGTACATGATAGTTAAGAAGCTATAAAATATGTTAAACATTCTATGAATATAAGTATATGGTTAGAGTTTTAGCTCTAGTTTTGGATAGAGATCAGTATTTTTTAAATCCCAGGCTATGACCCATCATGAAATAATTCAGCCAGCACTTTTACTAATGAAATAGAATACATTAGACTAGAATAAAACAGAAAACAAGCACATTACACAGAGTAAGGATTCAATTGTATATGTACTCATGTGTGTATGTACTGGGTAGACATTTATTACTGTAGGAATATAGCAGAATTTTAGAAATTTCCAAATGCAACTAAATAA... |
Task1_train_38984 | Chromosome 7 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | AAGCTATAAAATATGTTAAACATTCTATGAATATAAGTATATGGTTAGAGTTTTAGCTCTAGTTTTGGATAGAGATCAGTATTTTTTAAATCCCAGGCTATGACCCATCATGAAATAATTCAGCCAGCACTTTTACTAATGAAATAGAATACATTAGACTAGAATAAAACAGAAAACAAGCACATTACACAGAGTAAGGATTCAATTGTATATGTACTCATGTGTGTATGTACTGGGTAGACATTTATTACTGTAGGAATATAGCAGAATTTTAGAAATTTCCAAATGCAACTAAATAAATCATATGTAACAATTTCACT... | AAGCTATAAAATATGTTAAACATTCTATGAATATAAGTATATGGTTAGAGTTTTAGCTCTAGTTTTGGATAGAGATCAGTATTTTTTAAATCCCAGGCTATGACCCATCATGAAATAATTCAGCCAGCACTTTTACTAATGAAATAGAATACATTAGACTAGAATAAAACAGAAAACAAGCACATTACACAGAGTAAGGATTCAATTGTATATGTACTCATGTGTGTATGTACTGGGTAGACATTTATTACTGTAGGAATATAGCAGAATTTTAGAAATTTCCAAATGCAACTAAATAAATCATATGTAACAATTTCACT... |
Task1_train_38985 | Here’s a variant located on Chromosome 7. What is the predicted biological effect — harmless or disease-causing? | Benign | GTTTATTGCAGCACTATTCACAGTAACCAAAATATGGAATAAGCCTAAGTGCTCATCAATGAATGAATAAAGAAAATGTGATATATATACACAATGGTATATTATTCAGCCATGTAAAAGAATAAAATCCTGCCATTTTCAGCAACATGGATGGAACTGGAGGTCATTACATTAAATGAAACAAGCTAAGCACAGAATGACAAATATTGTATGTTTTCACTTATATGTGGGAGCTAAAAATGTGCATCTCATGAAGACAGAGAGTAGCTTGGTGGTTACCAGATGCCAGGAGGGGTAGCAAAAGGGAAACAAAAGAGAAG... | GTTTATTGCAGCACTATTCACAGTAACCAAAATATGGAATAAGCCTAAGTGCTCATCAATGAATGAATAAAGAAAATGTGATATATATACACAATGGTATATTATTCAGCCATGTAAAAGAATAAAATCCTGCCATTTTCAGCAACATGGATGGAACTGGAGGTCATTACATTAAATGAAACAAGCTAAGCACAGAATGACAAATATTGTATGTTTTCACTTATATGTGGGAGCTAAAAATGTGCATCTCATGAAGACAGAGAGTAGCTTGGTGGTTACCAGATGCCAGGAGGGGTAGCAAAAGGGAAACAAAAGAGAAG... |
Task1_train_38986 | Given this context: Chromosome 7 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | GCCACATTTTCTTAATCCAGTCTATCATTGTTGGACATTTGGGTTGGTTCCAAGTCTTTGCTATTGTGAATAGTGCCGCAATAAACATACGTGTGCATGTATCATCACTGGCCATCAGAGAAATGCAAATCAAAACCACAATGAGATACTGTTGTTCTATACATTTAATTGCATCTTCAATGAATTTAAGGTTCTAATTATTTACTTTGTTTTCCCTTTTTAGTGTTAAATTTGTGTTTTAAAACAAACATGTTTATTAGGCAAATTTTGAGTGGAGAAGTTTTTGTTTTTATTGTTGTTATTATTATCATCATTATTAT... | GCCACATTTTCTTAATCCAGTCTATCATTGTTGGACATTTGGGTTGGTTCCAAGTCTTTGCTATTGTGAATAGTGCCGCAATAAACATACGTGTGCATGTATCATCACTGGCCATCAGAGAAATGCAAATCAAAACCACAATGAGATACTGTTGTTCTATACATTTAATTGCATCTTCAATGAATTTAAGGTTCTAATTATTTACTTTGTTTTCCCTTTTTAGTGTTAAATTTGTGTTTTAAAACAAACATGTTTATTAGGCAAATTTTGAGTGGAGAAGTTTTTGTTTTTATTGTTGTTATTATTATCATCATTATTAT... |
Task1_train_38987 | A variant affecting Chromosome 7 has been observed. Determine if it's benign or associated with disease. | Benign | GGGCAGGGTTGCGGCCTTCATTGTTTAGGTTCCTTTCACCTGACTCTGCTTGAGAGAGACCTTTCCTGACCATCTCATCTAAAGGAGTCTTCCTCAAACCAAGCAACTTTCTATTATTTTACCCAGATTATTTTTTTACTGTTCTTTTCACAGTCAGCAATTATTTACTCATTTACTCCTGGTGTTTTAGTGGTAGTAACTAACCATTCCCTCTCTCTGCTCCAGAAAAAAATCAGTTAAGAAATGCACACAAGAATCAGATATAATTTTAAAATATATATATTTTATATATTTTGCTAGTAAGGCTTATTGAAAAGCAT... | GGGCAGGGTTGCGGCCTTCATTGTTTAGGTTCCTTTCACCTGACTCTGCTTGAGAGAGACCTTTCCTGACCATCTCATCTAAAGGAGTCTTCCTCAAACCAAGCAACTTTCTATTATTTTACCCAGATTATTTTTTTACTGTTCTTTTCACAGTCAGCAATTATTTACTCATTTACTCCTGGTGTTTTAGTGGTAGTAACTAACCATTCCCTCTCTCTGCTCCAGAAAAAAATCAGTTAAGAAATGCACACAAGAATCAGATATAATTTTAAAATATATATATTTTATATATTTTGCTAGTAAGGCTTATTGAAAAGCAT... |
Task1_train_38988 | Given this context: Chromosome 7 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CACTTCTTCATGACCTGGTCCCCTTCTGAATGCATCTACCTCCACCACTGTGCCTCCTGCGCTTAGAACAGTGGCTAAAACAGATCATGCACTCCAGGATCGTTTGTTAAAGGATGGATGAAGTACAAATTGACACTGGATAATATTGTTCTCTTATCGAATTAGCAAAGGTTGAAAATAAAAATACATGGTTGTGATGACCATGTGGGAAAGAGGCATGATTCTGAGGTACACATCAGTGATATATTATATTGGTATAAAATAATAGAATTTATATAGATAAAAATTAGTAGAATTTGTATTGGTAAATTTTCTGAAGC... | CACTTCTTCATGACCTGGTCCCCTTCTGAATGCATCTACCTCCACCACTGTGCCTCCTGCGCTTAGAACAGTGGCTAAAACAGATCATGCACTCCAGGATCGTTTGTTAAAGGATGGATGAAGTACAAATTGACACTGGATAATATTGTTCTCTTATCGAATTAGCAAAGGTTGAAAATAAAAATACATGGTTGTGATGACCATGTGGGAAAGAGGCATGATTCTGAGGTACACATCAGTGATATATTATATTGGTATAAAATAATAGAATTTATATAGATAAAAATTAGTAGAATTTGTATTGGTAAATTTTCTGAAGC... |
Task1_train_38989 | This genomic variant is located on Chromosome 7. Can you determine its pathogenicity and name any linked disease? | Benign | AGAGGCATGATTCTGAGGTACACATCAGTGATATATTATATTGGTATAAAATAATAGAATTTATATAGATAAAAATTAGTAGAATTTGTATTGGTAAATTTTCTGAAGCAAAGCTGGAAATAGATATCAAAAGCTTTGAAATTTCAATATATTTAGCACCTGCAAATTCACTTTTAGAATACATTCTCAATTAAAAATCATCAATATAAGCCAAACATAAGCTTGTAAGAATATTTATCTCAATGCTACCAAACATAAGAGAAATAGAAACCAAAAATTTCTGACAAGAAAAATGATTCAATAAATTATAATAAAAAGGA... | AGAGGCATGATTCTGAGGTACACATCAGTGATATATTATATTGGTATAAAATAATAGAATTTATATAGATAAAAATTAGTAGAATTTGTATTGGTAAATTTTCTGAAGCAAAGCTGGAAATAGATATCAAAAGCTTTGAAATTTCAATATATTTAGCACCTGCAAATTCACTTTTAGAATACATTCTCAATTAAAAATCATCAATATAAGCCAAACATAAGCTTGTAAGAATATTTATCTCAATGCTACCAAACATAAGAGAAATAGAAACCAAAAATTTCTGACAAGAAAAATGATTCAATAAATTATAATAAAAAGGA... |
Task1_train_38990 | Here is a genetic alteration on Chromosome 7. Based on the data, is it a benign variant or a cause of disease? | Benign | AAATTCAGTAAATTGTGACAGAATATTGTGCCCCTTTAAAATAATGTCCATAAAATATAATTTCGATACAGGAAAAGTATTATATTAAGTGAAAAATTGTAATGTTTAAATACTCTGTACAATACCCTATTTTAATATATAAATTTGAGGATCTACGTATTTACTAAAATAAAAGACATCAAAATTGTTTTTTTAAAAGTATCCTGTTGGATTTGAACCTTTAGCCTGATTTGAAAATAAAGATAGTCCTCAGGCTGTTTCTGGAATAAATGTGAAGTGTTAACAGAACAGCACCAGGTCACATGGTTTCTCCACCTGAT... | AAATTCAGTAAATTGTGACAGAATATTGTGCCCCTTTAAAATAATGTCCATAAAATATAATTTCGATACAGGAAAAGTATTATATTAAGTGAAAAATTGTAATGTTTAAATACTCTGTACAATACCCTATTTTAATATATAAATTTGAGGATCTACGTATTTACTAAAATAAAAGACATCAAAATTGTTTTTTTAAAAGTATCCTGTTGGATTTGAACCTTTAGCCTGATTTGAAAATAAAGATAGTCCTCAGGCTGTTTCTGGAATAAATGTGAAGTGTTAACAGAACAGCACCAGGTCACATGGTTTCTCCACCTGAT... |
Task1_train_38991 | A mutation on Chromosome 7 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCTTTCTCTGCTCGTTTTCCATTCCACTTTCTGACTCCTGTGCCATCTCCTGTCTCTCCCGCCCCCTAGCCTCTTTCCTTTGTTCCCTTCCTGACCTGTTCTTTCCTACTTTAGTACCTCTCAGGTCCCTTTCCTCCAATCTCCAGATCTGTGCCTTACCTTTTCTTTTCTGTTTAGATGTATTTTAGGATAGATTTTTCTTCTGTGGTTATCTTTCTCTTTCATCACCCAGTCAATGTTTTGCTGCTTCTTATACTACTGTCTTCACCCTTCATTCATCTTTCTGGT... | CTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCTTTCTCTGCTCGTTTTCCATTCCACTTTCTGACTCCTGTGCCATCTCCTGTCTCTCCCGCCCCCTAGCCTCTTTCCTTTGTTCCCTTCCTGACCTGTTCTTTCCTACTTTAGTACCTCTCAGGTCCCTTTCCTCCAATCTCCAGATCTGTGCCTTACCTTTTCTTTTCTGTTTAGATGTATTTTAGGATAGATTTTTCTTCTGTGGTTATCTTTCTCTTTCATCACCCAGTCAATGTTTTGCTGCTTCTTATACTACTGTCTTCACCCTTCATTCATCTTTCTGGT... |
Task1_train_38992 | With a mutation on Chromosome 7, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | AGAACTGTCTACTTGCTATCCTCGGAGTGCTCCCCAGCCCCGCCCCCCATACACAAAAACAAGAGCTGTGGGAAAATAAGTCCTAGTTCACAATACTAGAGAAGTGACTTCAGATATTCTCAGGCTTCTCTTGTGATCCTGTCCCTATGGGGCCCAACTTCCAGAGAAAGGCCCAGACTCAGATTTGCTCAGAGTCAGTCATGGGTTTGGGAATAGAATATGGTTAAATGTCAGGACCGAAGGAAAAGCCCAAGATGCCCAGTTCCTTCTTTAGTGGGAGAGATGAGCCCAGGGAAGAGGCCCTCCATGTGGTCATGCCT... | AGAACTGTCTACTTGCTATCCTCGGAGTGCTCCCCAGCCCCGCCCCCCATACACAAAAACAAGAGCTGTGGGAAAATAAGTCCTAGTTCACAATACTAGAGAAGTGACTTCAGATATTCTCAGGCTTCTCTTGTGATCCTGTCCCTATGGGGCCCAACTTCCAGAGAAAGGCCCAGACTCAGATTTGCTCAGAGTCAGTCATGGGTTTGGGAATAGAATATGGTTAAATGTCAGGACCGAAGGAAAAGCCCAAGATGCCCAGTTCCTTCTTTAGTGGGAGAGATGAGCCCAGGGAAGAGGCCCTCCATGTGGTCATGCCT... |
Task1_train_38993 | A mutation located on Chromosome 7 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GCTTACGGTGGACACTCCAGCTCATTTGTCAAGCAAGGATAGGAAACAAACAAAAACACCTGATACAACATTCAGAAGTAACACAGGCCACCTGCTTCCTTCAGGACCCCCACACAGAGTGTGAAGAAAAGGGAAGCGCCAGCCCTCTTTCTTCCTTCTCATATCAACAAGACGAGCCTACACAGGGGAAACGTCTAACTCTCCCCTCAGTCTACAGAGTCCACACTCTTTCCCAAACCCCCAACCCCTGTCCTCTCAGCGAGCCCAATCCTATCCCACCCAAGCAGCCTCTTTTCACTCTTTGACCCCCCAACTAGGGG... | GCTTACGGTGGACACTCCAGCTCATTTGTCAAGCAAGGATAGGAAACAAACAAAAACACCTGATACAACATTCAGAAGTAACACAGGCCACCTGCTTCCTTCAGGACCCCCACACAGAGTGTGAAGAAAAGGGAAGCGCCAGCCCTCTTTCTTCCTTCTCATATCAACAAGACGAGCCTACACAGGGGAAACGTCTAACTCTCCCCTCAGTCTACAGAGTCCACACTCTTTCCCAAACCCCCAACCCCTGTCCTCTCAGCGAGCCCAATCCTATCCCACCCAAGCAGCCTCTTTTCACTCTTTGACCCCCCAACTAGGGG... |
Task1_train_38994 | A mutation on Chromosome 7 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TTACAAACATGAAAGAGTCCCAAAGTATATTTATAGGTTAATGCCAATTCTTCACCTTAACAAATATAAAAAGCTAGCTCAATGATAGTGAATTACTTTGTGTAATTTGTTTGCTTTATGCTTCTCTCTGTGATTCAGCTGAGACATAATCCACAGAATTCAATAAATACAGCTAGTGATTAATGCCATTAGGGTCACTAATAGGTTGTCTGATCCTCCCAAGTTTTCCAAAGCAAAGAGTAATAAGCTGCCTAGCTACAGTTTCTGCTAGTAGAGTGTTTTTCATCTTGATTCTGCCTTTCCAATACAGCTTCCCTCAC... | TTACAAACATGAAAGAGTCCCAAAGTATATTTATAGGTTAATGCCAATTCTTCACCTTAACAAATATAAAAAGCTAGCTCAATGATAGTGAATTACTTTGTGTAATTTGTTTGCTTTATGCTTCTCTCTGTGATTCAGCTGAGACATAATCCACAGAATTCAATAAATACAGCTAGTGATTAATGCCATTAGGGTCACTAATAGGTTGTCTGATCCTCCCAAGTTTTCCAAAGCAAAGAGTAATAAGCTGCCTAGCTACAGTTTCTGCTAGTAGAGTGTTTTTCATCTTGATTCTGCCTTTCCAATACAGCTTCCCTCAC... |
Task1_train_38995 | A variant was discovered on Chromosome 7. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | AGATAAAGAGCCAACTAAATATTGTGCATGGTGTTATCAAGAATCAAATTCATCGATATGATTCAAATATATCATGGAAAAGGATATTATATTAGTTTTAACTAAACATCAAATTTCTACCAGTATCCAGATAATTTTCCTGTAAATGTACTACTGTAAATTTTATGTATATGTGTGTGTTTATGTGTATATATAAATTATACATATGTATTTATTCTATCTACAGGAAATATTTTGTAATGCAGAGTACCACAAGTACACATGTTGCTTCAAGTATCTTGCAAACACTGTAAACAAAGTGTAGTGGCTCATCCGCTACA... | AGATAAAGAGCCAACTAAATATTGTGCATGGTGTTATCAAGAATCAAATTCATCGATATGATTCAAATATATCATGGAAAAGGATATTATATTAGTTTTAACTAAACATCAAATTTCTACCAGTATCCAGATAATTTTCCTGTAAATGTACTACTGTAAATTTTATGTATATGTGTGTGTTTATGTGTATATATAAATTATACATATGTATTTATTCTATCTACAGGAAATATTTTGTAATGCAGAGTACCACAAGTACACATGTTGCTTCAAGTATCTTGCAAACACTGTAAACAAAGTGTAGTGGCTCATCCGCTACA... |
Task1_train_38996 | A genomic change on Chromosome 7 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GCGGATCACGGATGTCAGGGGATGGAGACCATCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAGAATACAAAAAATTAGCCAGAAGTGGTGGCAGACGCCTGTAGTCCCTGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACACAGGAGGTGGAGTTTGCAGTGATCTGAGATGGCGCCCCTGCACTCCAGCCTTGGTGACAGAGCGAGATTCCATCTCAAGAAAAAAAAAAAACGAGTAATGTCAAAGATTGACAGTCTGAGAGACAGATGAGGGTTTGCCAGAATAGCCTGGAAAATCTTATAATGTTAG... | GCGGATCACGGATGTCAGGGGATGGAGACCATCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAGAATACAAAAAATTAGCCAGAAGTGGTGGCAGACGCCTGTAGTCCCTGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACACAGGAGGTGGAGTTTGCAGTGATCTGAGATGGCGCCCCTGCACTCCAGCCTTGGTGACAGAGCGAGATTCCATCTCAAGAAAAAAAAAAAACGAGTAATGTCAAAGATTGACAGTCTGAGAGACAGATGAGGGTTTGCCAGAATAGCCTGGAAAATCTTATAATGTTAG... |
Task1_train_38997 | Located on Chromosome 7, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | ACATGTCATCAATTTATTTATTTATTTATTTTTTGAGGTGGAGTCTCACTCTGTCCCTCAGGCTGGAGTGCAGTGGCGCCATCTGGGCTCACTGCAACTTCTGCCTTGCCGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCGTGCCACTACGCCCGGGTCCTTTTGTATTTTTAGTAGAGAGGGGGGTTTCACCGTGTTTGCCGGGATGGTCTCAATCTCCTGACCTCGTGATCCGCCCGCTGGGATCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCTCATGTAAT... | ACATGTCATCAATTTATTTATTTATTTATTTTTTGAGGTGGAGTCTCACTCTGTCCCTCAGGCTGGAGTGCAGTGGCGCCATCTGGGCTCACTGCAACTTCTGCCTTGCCGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCGTGCCACTACGCCCGGGTCCTTTTGTATTTTTAGTAGAGAGGGGGGTTTCACCGTGTTTGCCGGGATGGTCTCAATCTCCTGACCTCGTGATCCGCCCGCTGGGATCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCTCATGTAAT... |
Task1_train_38998 | This mutation is located on Chromosome 7. Is it associated with a disease or is it a benign polymorphism? | Benign | GAACCCAGGCAGCGGAGGTTGCAGTAAGCTGAGATGGCACCACTGTACTCCAGCCTGGGCGACAGAGCGAGACTCTGTCTCAAGAAATAAATAATTAATTAATTAATAATGTGATTTCCCTTAAAGATTTCTTTTTTTTTTTTTTTGAGACGGAGTTTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCGCGAAGTTGGGTTGCTGTAAGCTCCGCCTCCTGGGTTCACGCCATTCTGCTGCCTCAGCCTCCGAAGTAGCTGAGACTACAGGCGCCCGCCACCACGCCTGGCTAATTTTTTCTATTTTTAGTAGAGACAG... | GAACCCAGGCAGCGGAGGTTGCAGTAAGCTGAGATGGCACCACTGTACTCCAGCCTGGGCGACAGAGCGAGACTCTGTCTCAAGAAATAAATAATTAATTAATTAATAATGTGATTTCCCTTAAAGATTTCTTTTTTTTTTTTTTTGAGACGGAGTTTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCGCGAAGTTGGGTTGCTGTAAGCTCCGCCTCCTGGGTTCACGCCATTCTGCTGCCTCAGCCTCCGAAGTAGCTGAGACTACAGGCGCCCGCCACCACGCCTGGCTAATTTTTTCTATTTTTAGTAGAGACAG... |
Task1_train_38999 | Here is a genetic alteration on Chromosome 7. Based on the data, is it a benign variant or a cause of disease? | Benign | GCCTGGGCAACATAGTGAGACCCTGTCTCAACAAAAATTTATTTTTTATTTTTTATTTTTATTTATTTATTTTTTGAGTCAGAGTCTCGCTCTGTCGCCAGGCTGGAGTGCAGTGGCAGGATCTCAGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGCGTGCCACCATGCCCAGCTAATTTTCGTATTTTTAGTAGAGATGGGGTTTCACTATGTTGGGCAGGATGGTCTCGATCTCTTGACCTCGTGATCCACCCACCTCGGCCTCCCATAGTG... | GCCTGGGCAACATAGTGAGACCCTGTCTCAACAAAAATTTATTTTTTATTTTTTATTTTTATTTATTTATTTTTTGAGTCAGAGTCTCGCTCTGTCGCCAGGCTGGAGTGCAGTGGCAGGATCTCAGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGCGTGCCACCATGCCCAGCTAATTTTCGTATTTTTAGTAGAGATGGGGTTTCACTATGTTGGGCAGGATGGTCTCGATCTCTTGACCTCGTGATCCACCCACCTCGGCCTCCCATAGTG... |
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