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_39900 | Assess the clinical impact of this variant found on Chromosome 10. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CAGGAGATCGAGACCATCCTGCCTAACACGGTGAAACCCCATCTGTACTAAAAATACAAAAAAATCAGCCAGGTGTGGTGGTGGGCACCTGTAGTCCTAGCTACTTGGGAGGCTGAGGCAGGAGAATGGTATGAACTCGGGAGGCGGAGCTTGCAGAGAGCCGAGATTGTGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCATCTCAAAAAAAAAAAAAAAAAGAAAAAAAAAAAGAAAGAAATACTGATAGGACAATGCTCAATAAGTTGACATATTTCAAAATATTAAGGTTTTTTAAGTTTTAATGACAC... | CAGGAGATCGAGACCATCCTGCCTAACACGGTGAAACCCCATCTGTACTAAAAATACAAAAAAATCAGCCAGGTGTGGTGGTGGGCACCTGTAGTCCTAGCTACTTGGGAGGCTGAGGCAGGAGAATGGTATGAACTCGGGAGGCGGAGCTTGCAGAGAGCCGAGATTGTGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCATCTCAAAAAAAAAAAAAAAAAGAAAAAAAAAAAGAAAGAAATACTGATAGGACAATGCTCAATAAGTTGACATATTTCAAAATATTAAGGTTTTTTAAGTTTTAATGACAC... |
Task1_train_39901 | Mutation context: Chromosome 10. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | AATAAACATGCACTGTGGGAATCACTCATAAGATGATTTACAGTAAAATTTGTGGATGGAAAAATAGGAACCAGGATGGTTGCCTACCAACAGTACTTAATAAATGTGCTTTGGGGCTTCAAAGGGAGGAATTAGGAAGAAAGAAGGGAAAATAACAAGAAGAGAAAAGCTTTAATGAGAGAAAGTGGACAGGTATCCTAAAGGAGTCCATATTTCCACAGAAGGAAAGAAGAATTAATGACAACAAAATAGCCAAAACTTGTAGGGCTCACCATGTTCAAAGCACTTAGTAAATCTCCTACCTTTGGTTTTAAAATCTC... | AATAAACATGCACTGTGGGAATCACTCATAAGATGATTTACAGTAAAATTTGTGGATGGAAAAATAGGAACCAGGATGGTTGCCTACCAACAGTACTTAATAAATGTGCTTTGGGGCTTCAAAGGGAGGAATTAGGAAGAAAGAAGGGAAAATAACAAGAAGAGAAAAGCTTTAATGAGAGAAAGTGGACAGGTATCCTAAAGGAGTCCATATTTCCACAGAAGGAAAGAAGAATTAATGACAACAAAATAGCCAAAACTTGTAGGGCTCACCATGTTCAAAGCACTTAGTAAATCTCCTACCTTTGGTTTTAAAATCTC... |
Task1_train_39902 | A variant on Chromosome 10 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GATAGGCTGGATAAAGAAAATGTGGCACCTATACACCATGGAATACTTTGTAGCCATAAAAAAGGATGAGTTCATGTACTTTGAAGGGACATGGATGAAGCTGGAAACCATCATTCTCAGCAAACTAACACAGGAACAAAAAACCAAACACCGCATATTCTCACTCGTAAGTGGGAGTTGAACAATGAGAACGCATGGACACAGGGAGGGGAACATCACACACCGGTGCCTGTCGAGGGGTGGGGGGCTAAGGGAGGGATAGCATTAGGAGAAATACCTTATGTAGATGACGGGTTGATGAGTGCAGCAAACCACCATGG... | GATAGGCTGGATAAAGAAAATGTGGCACCTATACACCATGGAATACTTTGTAGCCATAAAAAAGGATGAGTTCATGTACTTTGAAGGGACATGGATGAAGCTGGAAACCATCATTCTCAGCAAACTAACACAGGAACAAAAAACCAAACACCGCATATTCTCACTCGTAAGTGGGAGTTGAACAATGAGAACGCATGGACACAGGGAGGGGAACATCACACACCGGTGCCTGTCGAGGGGTGGGGGGCTAAGGGAGGGATAGCATTAGGAGAAATACCTTATGTAGATGACGGGTTGATGAGTGCAGCAAACCACCATGG... |
Task1_train_39903 | A variant found on Chromosome 10 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CTGGCTACAAAACATTCCACCATTCTGGTTTATGAAATTAAAACTTCCAAAGCCAGTTTTATGATTTTTTGTGCAAACTTTTCAGAAGAATTCAGAGGAGTTCATGGAACCGCTCACTGAAATTCAGTTCTAGTGTTCTGCAAAGCCTGAGAGGATGAACCATTCAGAGGTACTGATAGTTCTTTAGAACCAGAGAATCACCATGAAGGCTTTAACAGAAAGGGCCCCAAATTTCCCTGAAAATTATAGTTACATTCTTGCGTATCTGAGAAAATCATGATGCTCGGCTTCATGTTTTAGTCTCGTGATCGGAGAGCCAG... | CTGGCTACAAAACATTCCACCATTCTGGTTTATGAAATTAAAACTTCCAAAGCCAGTTTTATGATTTTTTGTGCAAACTTTTCAGAAGAATTCAGAGGAGTTCATGGAACCGCTCACTGAAATTCAGTTCTAGTGTTCTGCAAAGCCTGAGAGGATGAACCATTCAGAGGTACTGATAGTTCTTTAGAACCAGAGAATCACCATGAAGGCTTTAACAGAAAGGGCCCCAAATTTCCCTGAAAATTATAGTTACATTCTTGCGTATCTGAGAAAATCATGATGCTCGGCTTCATGTTTTAGTCTCGTGATCGGAGAGCCAG... |
Task1_train_39904 | A mutation on Chromosome 10 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TGTTTTCACTGATTCCCATTCTCTGTGTCCCTGTGACACCCAATTTCACCCCACACAACATAGCTCATGTCTTTAACTCTTGTATCTGTTCTCCCATTGGGGTTGGTCTTGTCTCCTCAGCTGCAAGGTGAGCAGTTCATAAGTGGAGACAGTATTTTACACTTTCATATTTTTCCATAGGGTCTACTATTGTCCTAAACATATAACAACAACCTCTCAATAAATGTGTTGATTCCAAATCAGGAGTTTAAGTGAGGGGCAGAAGAGTCAAAAGTGACTTTATGGAAGAAGTTGAGAGGGAAGTGCTCCTGAGGGACAGA... | TGTTTTCACTGATTCCCATTCTCTGTGTCCCTGTGACACCCAATTTCACCCCACACAACATAGCTCATGTCTTTAACTCTTGTATCTGTTCTCCCATTGGGGTTGGTCTTGTCTCCTCAGCTGCAAGGTGAGCAGTTCATAAGTGGAGACAGTATTTTACACTTTCATATTTTTCCATAGGGTCTACTATTGTCCTAAACATATAACAACAACCTCTCAATAAATGTGTTGATTCCAAATCAGGAGTTTAAGTGAGGGGCAGAAGAGTCAAAAGTGACTTTATGGAAGAAGTTGAGAGGGAAGTGCTCCTGAGGGACAGA... |
Task1_train_39905 | A variant was discovered on Chromosome 10. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CATTGTATTCAATGGTTGTAGATTTATAATTCAAATTATTAAAATTATAAGAATTCTTAAAAACCTTTAAAGATTTAAAAATATTCATATTCTTTGATTTAAGTAGAATCCTCTTCTAAGACTCTGCCTAAGAAAATTATCATATTTGTGCATGGCAAAATGTGTACATGAAAAAAAGTTGGAAGAAAAAAACGCCCAAATGTTCATCATGGTCCTCTGTGTGATAAGATCAAAGGTATTTTTTTCTATTTTTTCCATATTTTTGTAGTGATATTTTATAAGCAGCATATATTGCTTTGCTGCTTATAAAATATAACTAC... | CATTGTATTCAATGGTTGTAGATTTATAATTCAAATTATTAAAATTATAAGAATTCTTAAAAACCTTTAAAGATTTAAAAATATTCATATTCTTTGATTTAAGTAGAATCCTCTTCTAAGACTCTGCCTAAGAAAATTATCATATTTGTGCATGGCAAAATGTGTACATGAAAAAAAGTTGGAAGAAAAAAACGCCCAAATGTTCATCATGGTCCTCTGTGTGATAAGATCAAAGGTATTTTTTTCTATTTTTTCCATATTTTTGTAGTGATATTTTATAAGCAGCATATATTGCTTTGCTGCTTATAAAATATAACTAC... |
Task1_train_39906 | This sequence change occurs on Chromosome 10. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | ATGCACTAAATTCTTTGGGAAGGAAGACCCATAATCTAAACTATTTTCAGTTTACCTATAATATTATCCAAAATAAAGCCATTCTGCTTATCGAATCAAATTTCCTTTGGGAAAAAAAGCCTTTAAATTATAATTTATATAAGCATTTATAACTGTGATACCTACAGAGGTTGGAGATAATAGAAACTCTTGGTACTGAAAGCCACAATTTTCTATTGTTTGTATCAAGAGGTCTCTAAAAAGAAAAAAAAAAAACTTTAATTCTTACTTGGAAAGGCAGTTCTTATTTAAATAATGTACACAAAAGCTGGGTTTCTTTT... | ATGCACTAAATTCTTTGGGAAGGAAGACCCATAATCTAAACTATTTTCAGTTTACCTATAATATTATCCAAAATAAAGCCATTCTGCTTATCGAATCAAATTTCCTTTGGGAAAAAAAGCCTTTAAATTATAATTTATATAAGCATTTATAACTGTGATACCTACAGAGGTTGGAGATAATAGAAACTCTTGGTACTGAAAGCCACAATTTTCTATTGTTTGTATCAAGAGGTCTCTAAAAAGAAAAAAAAAAAACTTTAATTCTTACTTGGAAAGGCAGTTCTTATTTAAATAATGTACACAAAAGCTGGGTTTCTTTT... |
Task1_train_39907 | An alteration has been detected on Chromosome 10. Is it pathogenic, and if so, what disease is involved? | Benign | AATGAGTAAAAATTATATTTCACAGTGAAGACAAAATAAAACACTTTTTTACTCAAAAGCACCAAGGTAATTTGTCCCTTTCCACATATAACCAACAAGAGACACTAAAGAAGGTTTTTCAGGAAGAAGAAAAATTATATCACATGCAAACTTTGATCTAAAACACAAGGATAAAAAGTGCTGAAAATTGTAGGTATATAGATAAATATAAAAGACTTTGTGCTTTTTAAAAGTTCTTTAATAGATATTTGACTATTTAATCCAAAAAACAGTAACAATGTATGTTGGTGCCTATAACATTCGTAGCAGTAAAGTGCAAG... | AATGAGTAAAAATTATATTTCACAGTGAAGACAAAATAAAACACTTTTTTACTCAAAAGCACCAAGGTAATTTGTCCCTTTCCACATATAACCAACAAGAGACACTAAAGAAGGTTTTTCAGGAAGAAGAAAAATTATATCACATGCAAACTTTGATCTAAAACACAAGGATAAAAAGTGCTGAAAATTGTAGGTATATAGATAAATATAAAAGACTTTGTGCTTTTTAAAAGTTCTTTAATAGATATTTGACTATTTAATCCAAAAAACAGTAACAATGTATGTTGGTGCCTATAACATTCGTAGCAGTAAAGTGCAAG... |
Task1_train_39908 | Given a variant located on Chromosome 10, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TGGTGGTCTCTTCACATGGACACGCCTAACAGAGATGGTATAAAAATGCTTTGAAAACCTAAGAAAAACATTCATTTAATTATTTGTTTATTCAACAAAAATTAATTGAGCAACTGCTATGTGCTGCACCCTTGTGATTGGCACCAGGGGATAGGCATGTGAACAAGACATTGTCCCATTCATTTTGGAGCTCAAAATCTGAAACACAGAATAAAGAATTATGGCACAAAAGACCCTATCCCACTTGTTCTCCTAATGGCAACTGCCTAATTTTCATTTATTCAAAAAATATAGTTAAGACTAGGGGAGAAAAAGAGCAC... | TGGTGGTCTCTTCACATGGACACGCCTAACAGAGATGGTATAAAAATGCTTTGAAAACCTAAGAAAAACATTCATTTAATTATTTGTTTATTCAACAAAAATTAATTGAGCAACTGCTATGTGCTGCACCCTTGTGATTGGCACCAGGGGATAGGCATGTGAACAAGACATTGTCCCATTCATTTTGGAGCTCAAAATCTGAAACACAGAATAAAGAATTATGGCACAAAAGACCCTATCCCACTTGTTCTCCTAATGGCAACTGCCTAATTTTCATTTATTCAAAAAATATAGTTAAGACTAGGGGAGAAAAAGAGCAC... |
Task1_train_39909 | This alteration on Chromosome 10 may affect genome function. Does it lead to a disease or is it benign? | Benign | GTGAGCCACCACACCAGGCCACAAGCTAGTGATTTTTAAGCAACTCACTTAACCTCTTTCATCTTAATGTAAATGAGAAATAATACTACTACTTTTGAATACTAAGTACTCAAAAAGTACTTTTAATTAGCAAAGGATTTAATAAGTAAAATTAATTGATTTATTACTAACATTAAGAATGCAGGGGGAGGAGGGAATTAAAAAAAAATGCAGTGGAAAACATGTTCTGGGCTGAGTGATTCTCTGGCCAGTGGGACTCAGTAGCTGGCAGCATGGTGAACTGGGAAGCTGCTACTGGTACAGGCCAGAGTCTACATCTC... | GTGAGCCACCACACCAGGCCACAAGCTAGTGATTTTTAAGCAACTCACTTAACCTCTTTCATCTTAATGTAAATGAGAAATAATACTACTACTTTTGAATACTAAGTACTCAAAAAGTACTTTTAATTAGCAAAGGATTTAATAAGTAAAATTAATTGATTTATTACTAACATTAAGAATGCAGGGGGAGGAGGGAATTAAAAAAAAATGCAGTGGAAAACATGTTCTGGGCTGAGTGATTCTCTGGCCAGTGGGACTCAGTAGCTGGCAGCATGGTGAACTGGGAAGCTGCTACTGGTACAGGCCAGAGTCTACATCTC... |
Task1_train_39910 | A genomic change on Chromosome 10 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TGTTAGTTGGGGAAGGTGTCACTGATGACGGTTTTCTAAAGCTACCTGTAGCGATGGTAGTATTATAAGGTGATAATAAGTGACAATTACTGTTAGTATTTTGAGACCACTGAAGCTTATGTATTTATTTGTCTCTGATTTTAGTTTACTACAGTCAGCATGTGCCAGGCACTGTGTTAGACACCTGAGAGTCTTCTTTAGCTTCAAGGTGCTTACTGAGTAGTAGGGGCAAACACATAAAAAAATATAATTTTATACAACATGATTTATAAATAAAGAAGATATATGCCTTGTACCTTAGGAGCCTCAGGGTTTGAGGA... | TGTTAGTTGGGGAAGGTGTCACTGATGACGGTTTTCTAAAGCTACCTGTAGCGATGGTAGTATTATAAGGTGATAATAAGTGACAATTACTGTTAGTATTTTGAGACCACTGAAGCTTATGTATTTATTTGTCTCTGATTTTAGTTTACTACAGTCAGCATGTGCCAGGCACTGTGTTAGACACCTGAGAGTCTTCTTTAGCTTCAAGGTGCTTACTGAGTAGTAGGGGCAAACACATAAAAAAATATAATTTTATACAACATGATTTATAAATAAAGAAGATATATGCCTTGTACCTTAGGAGCCTCAGGGTTTGAGGA... |
Task1_train_39911 | An alteration has been detected on Chromosome 10. Is it pathogenic, and if so, what disease is involved? | Benign | CTCAATTCACACTTAAACTTTAAAACTAATTAGTTACTTGTATAAAAGAAATTAGAAATGTATTGTGTCCTTTAAACAAACTCCTACTTACAGTAGGTAAGCATTTTATTAGTTATTCATAATAATTTATTTATTTTAAAATGTTTTCAAATTCAGTTCCACGCGCTTCAACAAATTTTTATTGACTTTGTCTCTTTGACCTTTAGAGCTATTCAGTCTAATGGCTCCTTTTAAGTTTTGTTTTATCACGTCATATGGCAGCTCAGCATGTTTGCTGAGTAAACTTTGTCAAGTCCTGATAATTTCTTAGCAACCAAAAT... | CTCAATTCACACTTAAACTTTAAAACTAATTAGTTACTTGTATAAAAGAAATTAGAAATGTATTGTGTCCTTTAAACAAACTCCTACTTACAGTAGGTAAGCATTTTATTAGTTATTCATAATAATTTATTTATTTTAAAATGTTTTCAAATTCAGTTCCACGCGCTTCAACAAATTTTTATTGACTTTGTCTCTTTGACCTTTAGAGCTATTCAGTCTAATGGCTCCTTTTAAGTTTTGTTTTATCACGTCATATGGCAGCTCAGCATGTTTGCTGAGTAAACTTTGTCAAGTCCTGATAATTTCTTAGCAACCAAAAT... |
Task1_train_39912 | This genomic variant is located on Chromosome 10. Can you determine its pathogenicity and name any linked disease? | Benign | TGGCTTAGCAGCCACTTAACCGCATGTGGCCACTGAGCACATGAGCTGTGGCTAGAGGAACAAATCATCTTCTGTGGCTGCCCCAGGGAACTCCCCTTCATTTCACTCAAGTTGGTTGTTTTCATGCTTTCAAATATGTTTAAAGTTCATCATTTCAGTTTTTGAAGGACAGCATTGGCTGATACTATTTTCAATTTCCTAGGTAGCAAAATTAAAATAACCCACCAGAGGGCTCCAAAGCTGTACTAAGCTTGCTTTCTTTTTCTTTTTCTTCTTTTTTTTTTTGTAACCACTGGAAGTGCACAGAATCTAAATTGTAT... | TGGCTTAGCAGCCACTTAACCGCATGTGGCCACTGAGCACATGAGCTGTGGCTAGAGGAACAAATCATCTTCTGTGGCTGCCCCAGGGAACTCCCCTTCATTTCACTCAAGTTGGTTGTTTTCATGCTTTCAAATATGTTTAAAGTTCATCATTTCAGTTTTTGAAGGACAGCATTGGCTGATACTATTTTCAATTTCCTAGGTAGCAAAATTAAAATAACCCACCAGAGGGCTCCAAAGCTGTACTAAGCTTGCTTTCTTTTTCTTTTTCTTCTTTTTTTTTTTGTAACCACTGGAAGTGCACAGAATCTAAATTGTAT... |
Task1_train_39913 | This sequence variant lies on Chromosome 10. Is it clinically significant, and what condition might it cause if any? | Benign | GTTGAGAGGTTTTGTTTTGAGGAGCATGAAGGATCTGATGTAAGAACTACCACCGGTGCTGGTGATCACAATATATGCAGCTGATTAAAGTTCCTCATTTATGCTACCTACATCCCTGGTAAGAATTTCATTCCTTCAACCAATACTTTTCATTTGAAAGCATCTCATTACGAAAGACTTCAATCTTTTAGGCTTCTGCATCTTGCAAAACAAATATGGTTCCAAAGAGCCTATCTTTTCAACAAATCTTTGGTTTGAGCCTGGATGAAACAGTTATTACAGAATCAACTGGAGAGGAAAAAATCTTCATCTAACACTGA... | GTTGAGAGGTTTTGTTTTGAGGAGCATGAAGGATCTGATGTAAGAACTACCACCGGTGCTGGTGATCACAATATATGCAGCTGATTAAAGTTCCTCATTTATGCTACCTACATCCCTGGTAAGAATTTCATTCCTTCAACCAATACTTTTCATTTGAAAGCATCTCATTACGAAAGACTTCAATCTTTTAGGCTTCTGCATCTTGCAAAACAAATATGGTTCCAAAGAGCCTATCTTTTCAACAAATCTTTGGTTTGAGCCTGGATGAAACAGTTATTACAGAATCAACTGGAGAGGAAAAAATCTTCATCTAACACTGA... |
Task1_train_39914 | A genomic variant on Chromosome 10 is under review. What is the biological outcome — benign or pathogenic? | Benign | CTCTCTGCACCACACTGCTGCTACTGGGGAGGTGGGAGAGGGGTGACATCAGAGATTCAAGACTGTTTTTTCTGCCTCTTCAGTGCCTATTTCAGTAATATGAAGTTAAAACCAGGTATAACGAGGGCTCACCTGAATTTTAGTTTGTATGAAGGTGCTTTTCTTGTGTAGATAGTTGTTAAATTGGTGTCCTTGTGGGGAGATGATTGGTGGAGGCTTCTATTCTGCCATCTTACTCTGCCTCCTCCAGTTTTTTTCTGTAGCTCTTTGAATATATCATTTCACTACCCTTCTGTCCCCCATTATTTAGATAAGAAATC... | CTCTCTGCACCACACTGCTGCTACTGGGGAGGTGGGAGAGGGGTGACATCAGAGATTCAAGACTGTTTTTTCTGCCTCTTCAGTGCCTATTTCAGTAATATGAAGTTAAAACCAGGTATAACGAGGGCTCACCTGAATTTTAGTTTGTATGAAGGTGCTTTTCTTGTGTAGATAGTTGTTAAATTGGTGTCCTTGTGGGGAGATGATTGGTGGAGGCTTCTATTCTGCCATCTTACTCTGCCTCCTCCAGTTTTTTTCTGTAGCTCTTTGAATATATCATTTCACTACCCTTCTGTCCCCCATTATTTAGATAAGAAATC... |
Task1_train_39915 | A variant on Chromosome 10 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TCTCTTCCCTCTGAAATCTCTTACCAGGGATAATGATGGTGGACCAATGATCCCCACTCCAGCAAAGCCTGAGCTGGTTAAAATTTTCCACAAGCCTCTGGCAGTTTCCTGCAGGGTCACTCTTGTTGCTTCGAGGCTCAATTGTTATTCAATGTTCTGAAAATCACAAAGGGAGCATTGGAAAAATAAAACCATTATGAGTTTTAATTGCCCTCATAATCTAATATCCTGGAAATATTTCAGGGCTTATGACTGAGTAGAGGCGGCGGCCCAGGCCTTTTTTCTAGGTCACAGCAGCGGTAGCAGAATTGTTTACTGCC... | TCTCTTCCCTCTGAAATCTCTTACCAGGGATAATGATGGTGGACCAATGATCCCCACTCCAGCAAAGCCTGAGCTGGTTAAAATTTTCCACAAGCCTCTGGCAGTTTCCTGCAGGGTCACTCTTGTTGCTTCGAGGCTCAATTGTTATTCAATGTTCTGAAAATCACAAAGGGAGCATTGGAAAAATAAAACCATTATGAGTTTTAATTGCCCTCATAATCTAATATCCTGGAAATATTTCAGGGCTTATGACTGAGTAGAGGCGGCGGCCCAGGCCTTTTTTCTAGGTCACAGCAGCGGTAGCAGAATTGTTTACTGCC... |
Task1_train_39916 | Given a variant located on Chromosome 10, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AAAAGCCAGGATAAAGACTAGTAATTTGGCTTCTAGAGCCAATACCTTGTCCTTGACCATAGCATATTTCTTCAATAAATCCATGAGATTCTTTCATGGCTAAAACATCTGAAAGTGATAAATGTCTAAATCAGACATTTCCAAAGGAATTTCTGTAGCCTGAATTTCATGGTGACCATAGCACCACTGATGGCTAGAATCTGTATTTTAGCGATAAAGGAGGAGAAACAAGTTGAACTACATTTTAAACTCCACAAGGATAGAGACTTTATCACACCACTATGTACCCAAGCCTAATCCATAATGGGCACTCAAATACT... | AAAAGCCAGGATAAAGACTAGTAATTTGGCTTCTAGAGCCAATACCTTGTCCTTGACCATAGCATATTTCTTCAATAAATCCATGAGATTCTTTCATGGCTAAAACATCTGAAAGTGATAAATGTCTAAATCAGACATTTCCAAAGGAATTTCTGTAGCCTGAATTTCATGGTGACCATAGCACCACTGATGGCTAGAATCTGTATTTTAGCGATAAAGGAGGAGAAACAAGTTGAACTACATTTTAAACTCCACAAGGATAGAGACTTTATCACACCACTATGTACCCAAGCCTAATCCATAATGGGCACTCAAATACT... |
Task1_train_39917 | This sequence change occurs on Chromosome 10. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GGAGTGTGAGTATAAAATGATGATACTGATTATATGTGTGGGTTATGAAGGCAACTTCATTTCTTTATAGTGATATTCCATTTATACATCCTATCACAGCCTATTGAGTTAACATTTTGACACTATTTAATTTTCATAGGCTGATATCTGTTTTTATAACTTCTCAGGTACTAAACAAGTTTCTTTTTTTATAAACTGAAGATTAAATTTTGTTTTAACTCAAAGATAAAACAAAGTAAAATGTAAAGAAAATGAATTTGAGAGTTATTCCAGGTTCTCAAGTGGATATGTAATGTAATTAGCTGTTCAATAATTATAGG... | GGAGTGTGAGTATAAAATGATGATACTGATTATATGTGTGGGTTATGAAGGCAACTTCATTTCTTTATAGTGATATTCCATTTATACATCCTATCACAGCCTATTGAGTTAACATTTTGACACTATTTAATTTTCATAGGCTGATATCTGTTTTTATAACTTCTCAGGTACTAAACAAGTTTCTTTTTTTATAAACTGAAGATTAAATTTTGTTTTAACTCAAAGATAAAACAAAGTAAAATGTAAAGAAAATGAATTTGAGAGTTATTCCAGGTTCTCAAGTGGATATGTAATGTAATTAGCTGTTCAATAATTATAGG... |
Task1_train_39918 | This variant is present on Chromosome 10. Is the change likely to result in a pathogenic outcome? | Benign | AACAAGTTTCTTTTTTTATAAACTGAAGATTAAATTTTGTTTTAACTCAAAGATAAAACAAAGTAAAATGTAAAGAAAATGAATTTGAGAGTTATTCCAGGTTCTCAAGTGGATATGTAATGTAATTAGCTGTTCAATAATTATAGGCCTTTGAGATCTAAGTTTAAAACCATCAATTTTTGAACCTCAAATTGATATCATTTCTGCATTTCTGATCTCTTGCTGCTATGAAAATATACAGCTATACATTAATAATTTTTACATGTATGATATTCATTATGGGAAAAGTATGTAGCAGCATACAAAGTTTTCTTATTGTT... | AACAAGTTTCTTTTTTTATAAACTGAAGATTAAATTTTGTTTTAACTCAAAGATAAAACAAAGTAAAATGTAAAGAAAATGAATTTGAGAGTTATTCCAGGTTCTCAAGTGGATATGTAATGTAATTAGCTGTTCAATAATTATAGGCCTTTGAGATCTAAGTTTAAAACCATCAATTTTTGAACCTCAAATTGATATCATTTCTGCATTTCTGATCTCTTGCTGCTATGAAAATATACAGCTATACATTAATAATTTTTACATGTATGATATTCATTATGGGAAAAGTATGTAGCAGCATACAAAGTTTTCTTATTGTT... |
Task1_train_39919 | A mutation located on Chromosome 10 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TGTGTGTGTGTGCATGTGTGCGCGTGTCTGCCTGTGTGTCTGTGTGTGTGTGCATGCCTGTGTGTCTGTGTGTGTGCGTGCATGTGTGCATGTGTGTGTGTGTGTGTGCATGGGTGTGTGCATGCGTGTCTGTGCACATGTGTGTATGATTCTGATAGACACCGAGGAGTGCAGAGCAGCAGATTTAAGGATTCATTTAAAGATTCATGAGTTTGGCCAGGCACGGTGGCTCACACCTGCAATCCTAGCACTTTGGGAGGCTGAGCCGGGCGGATCAGTTGAGGTCAGGAGTTCAAGACCTGCCTGGCCAACATGGTGAA... | TGTGTGTGTGTGCATGTGTGCGCGTGTCTGCCTGTGTGTCTGTGTGTGTGTGCATGCCTGTGTGTCTGTGTGTGTGCGTGCATGTGTGCATGTGTGTGTGTGTGTGTGCATGGGTGTGTGCATGCGTGTCTGTGCACATGTGTGTATGATTCTGATAGACACCGAGGAGTGCAGAGCAGCAGATTTAAGGATTCATTTAAAGATTCATGAGTTTGGCCAGGCACGGTGGCTCACACCTGCAATCCTAGCACTTTGGGAGGCTGAGCCGGGCGGATCAGTTGAGGTCAGGAGTTCAAGACCTGCCTGGCCAACATGGTGAA... |
Task1_train_39920 | A variant affecting Chromosome 10 has been observed. Determine if it's benign or associated with disease. | Benign | ATTTTATTTCTAACTTGTATTATTTACTGTTATTATCTTTAATTTTTGAGCAGTATATAATTTTGCTTTACCGAAGATTTCTAAACTTTACTTGATAAATCTTTTTTTTGAGACAGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCAGGATCTCAGCTCACTGCAACCTCAGCCTCCCAGATTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGATGCATGCCACCCTGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATATTGGCCAGGATGGTCTCGATCTCTTG... | ATTTTATTTCTAACTTGTATTATTTACTGTTATTATCTTTAATTTTTGAGCAGTATATAATTTTGCTTTACCGAAGATTTCTAAACTTTACTTGATAAATCTTTTTTTTGAGACAGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCAGGATCTCAGCTCACTGCAACCTCAGCCTCCCAGATTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGATGCATGCCACCCTGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATATTGGCCAGGATGGTCTCGATCTCTTG... |
Task1_train_39921 | This sequence change occurs on Chromosome 10. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | AGAAAGCAAATATGGTTTTGAAATTAGATATTTCATAGAAAGTATAAAAAACTTATAAGTTGTTTGTAATATTATTACCTCACATTCTTCTCCCTGTAGAAGAGGCATTTTCAGGATTCAAAATGATATTTTTATCATTGGGTTAAAATGCTCTTACAATTAGGTTAAATTCCCTATAATTTTATTATTACATTAAAATGCCCTTATAATTTTAAATTTTGTAATCTCATTTAGTGATTTAGTTTACACTTTTTTCCCTAAACTCATTGTTTACTTCCTAATTTATTTTACAAGGGTGTGTCTATGCGTTTTATTGCTAT... | AGAAAGCAAATATGGTTTTGAAATTAGATATTTCATAGAAAGTATAAAAAACTTATAAGTTGTTTGTAATATTATTACCTCACATTCTTCTCCCTGTAGAAGAGGCATTTTCAGGATTCAAAATGATATTTTTATCATTGGGTTAAAATGCTCTTACAATTAGGTTAAATTCCCTATAATTTTATTATTACATTAAAATGCCCTTATAATTTTAAATTTTGTAATCTCATTTAGTGATTTAGTTTACACTTTTTTCCCTAAACTCATTGTTTACTTCCTAATTTATTTTACAAGGGTGTGTCTATGCGTTTTATTGCTAT... |
Task1_train_39922 | With a mutation on Chromosome 10, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TGAGCAATTGCATATGTAGCAGTTACTGAGTGCTACATACTATTTATGAATTTTTAAAATATTTACTCATTTTGCTTTCACAATAACCTTATGAATTACATAGTATTATTATCTCCATATTATAAATTAGAATACAGAAATACCCAGATGTTAGGTCTTTTGTTCTAGTTATGTAACTACAAATGGCAGAGGCTGACTGTAGACAAGGTCAGGCCTTCCACCAGTCCACAGTGCAACTGCCATGCTACATTGTCTACCAAATTTTAGAAAATAATTAACCCTGACTATATTCTGTCTGAAGAAAGATACATTGTAGTTTC... | TGAGCAATTGCATATGTAGCAGTTACTGAGTGCTACATACTATTTATGAATTTTTAAAATATTTACTCATTTTGCTTTCACAATAACCTTATGAATTACATAGTATTATTATCTCCATATTATAAATTAGAATACAGAAATACCCAGATGTTAGGTCTTTTGTTCTAGTTATGTAACTACAAATGGCAGAGGCTGACTGTAGACAAGGTCAGGCCTTCCACCAGTCCACAGTGCAACTGCCATGCTACATTGTCTACCAAATTTTAGAAAATAATTAACCCTGACTATATTCTGTCTGAAGAAAGATACATTGTAGTTTC... |
Task1_train_39923 | This variant is present on Chromosome 10. Is the change likely to result in a pathogenic outcome? | Benign | CCCAAATGACATAGAAACGATGGTAAAACTCGTATGTTTTCTTTTTTAATTTTTAAAATTTAATTTAATTATTTGTAGAGACAAAGTCTCACTTTGTTGGCCAGGATGGTCTTGAACTCCTAGCATCATGTGATCCTCCCACCTTAGCCTCCTAAAATGTTGTGATTACAGGGGTGAAGCACTCCACCCAGCCTCATATGCTTTCATATTCTCCACCTTATAAACTACAAAGAGTAATTGGTTTATTTTGCACCTTGAGATAATTTTATCTGACTTGGGATAACTATAAGAATGTATCTATACAGAAACAAACAAACAAA... | CCCAAATGACATAGAAACGATGGTAAAACTCGTATGTTTTCTTTTTTAATTTTTAAAATTTAATTTAATTATTTGTAGAGACAAAGTCTCACTTTGTTGGCCAGGATGGTCTTGAACTCCTAGCATCATGTGATCCTCCCACCTTAGCCTCCTAAAATGTTGTGATTACAGGGGTGAAGCACTCCACCCAGCCTCATATGCTTTCATATTCTCCACCTTATAAACTACAAAGAGTAATTGGTTTATTTTGCACCTTGAGATAATTTTATCTGACTTGGGATAACTATAAGAATGTATCTATACAGAAACAAACAAACAAA... |
Task1_train_39924 | A genetic alteration is present on Chromosome 10. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | AGTTGTATTAACTCCTCCTTTAATTTCTAAGTTTATTTATCTGAGTCTTCTTTATTCTTTGTTCATCTAGCTAAGTGTCTGTCAGTTTTATCTTTTCAAAAAATGAACCATGTATTTTATTGACATTCTCTATGGTTTATTCTCTATATTATTTATTTATGTTCTAATCTTTATAATTATTTTTGTTCTGCTAACTTCGGCCTTAGTTCTTTTTCTTCTAGTTTTCTGTCAAATAAAGTTAGGATGTTTATTTAAGATCTTTCTTTTTTAACGTAGGTATTTATCACTATACACTTCCCTGTTAGTACTGCTTTTGCTGC... | AGTTGTATTAACTCCTCCTTTAATTTCTAAGTTTATTTATCTGAGTCTTCTTTATTCTTTGTTCATCTAGCTAAGTGTCTGTCAGTTTTATCTTTTCAAAAAATGAACCATGTATTTTATTGACATTCTCTATGGTTTATTCTCTATATTATTTATTTATGTTCTAATCTTTATAATTATTTTTGTTCTGCTAACTTCGGCCTTAGTTCTTTTTCTTCTAGTTTTCTGTCAAATAAAGTTAGGATGTTTATTTAAGATCTTTCTTTTTTAACGTAGGTATTTATCACTATACACTTCCCTGTTAGTACTGCTTTTGCTGC... |
Task1_train_39925 | This alteration on Chromosome 10 may affect genome function. Does it lead to a disease or is it benign? | Benign | TAACTCCTCCTTTAATTTCTAAGTTTATTTATCTGAGTCTTCTTTATTCTTTGTTCATCTAGCTAAGTGTCTGTCAGTTTTATCTTTTCAAAAAATGAACCATGTATTTTATTGACATTCTCTATGGTTTATTCTCTATATTATTTATTTATGTTCTAATCTTTATAATTATTTTTGTTCTGCTAACTTCGGCCTTAGTTCTTTTTCTTCTAGTTTTCTGTCAAATAAAGTTAGGATGTTTATTTAAGATCTTTCTTTTTTAACGTAGGTATTTATCACTATACACTTCCCTGTTAGTACTGCTTTTGCTGCATCTCACA... | TAACTCCTCCTTTAATTTCTAAGTTTATTTATCTGAGTCTTCTTTATTCTTTGTTCATCTAGCTAAGTGTCTGTCAGTTTTATCTTTTCAAAAAATGAACCATGTATTTTATTGACATTCTCTATGGTTTATTCTCTATATTATTTATTTATGTTCTAATCTTTATAATTATTTTTGTTCTGCTAACTTCGGCCTTAGTTCTTTTTCTTCTAGTTTTCTGTCAAATAAAGTTAGGATGTTTATTTAAGATCTTTCTTTTTTAACGTAGGTATTTATCACTATACACTTCCCTGTTAGTACTGCTTTTGCTGCATCTCACA... |
Task1_train_39926 | A mutation on Chromosome 10 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TCACTGAATGTGTTAGGAGTGTTCGCTCATTCTTGTTTTCTTTTGTTTTGTTTTAGGTTTCTGCCCACTTGGCTATAGGGAATGTCATAATGGAAAATGCTATAGGCTGGAACAAAGCTGTAACTTCGTAGATAACTGTGGAGATAATACTGATGAAAATGAGTGTGGTAGCTCCTGTACTTTTGAAAAAGGCTGGTGTGGCTGGCAAAACTCCCAGGCTGACAACTTTGATTGGGTTTTAGGGGTTGGCTCTCATCAAAGCTTAAGACCTCCCAAAGACCACACACTTGGAAATGAAAATGGTAGGTTATTAGATTGTT... | TCACTGAATGTGTTAGGAGTGTTCGCTCATTCTTGTTTTCTTTTGTTTTGTTTTAGGTTTCTGCCCACTTGGCTATAGGGAATGTCATAATGGAAAATGCTATAGGCTGGAACAAAGCTGTAACTTCGTAGATAACTGTGGAGATAATACTGATGAAAATGAGTGTGGTAGCTCCTGTACTTTTGAAAAAGGCTGGTGTGGCTGGCAAAACTCCCAGGCTGACAACTTTGATTGGGTTTTAGGGGTTGGCTCTCATCAAAGCTTAAGACCTCCCAAAGACCACACACTTGGAAATGAAAATGGTAGGTTATTAGATTGTT... |
Task1_train_39927 | A variant on Chromosome 10 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TGTTTTAGGTTTCTGCCCACTTGGCTATAGGGAATGTCATAATGGAAAATGCTATAGGCTGGAACAAAGCTGTAACTTCGTAGATAACTGTGGAGATAATACTGATGAAAATGAGTGTGGTAGCTCCTGTACTTTTGAAAAAGGCTGGTGTGGCTGGCAAAACTCCCAGGCTGACAACTTTGATTGGGTTTTAGGGGTTGGCTCTCATCAAAGCTTAAGACCTCCCAAAGACCACACACTTGGAAATGAAAATGGTAGGTTATTAGATTGTTGTAATTGCTTTCACATGATTTTCACAATGTACATCAAAATGTCTTTTC... | TGTTTTAGGTTTCTGCCCACTTGGCTATAGGGAATGTCATAATGGAAAATGCTATAGGCTGGAACAAAGCTGTAACTTCGTAGATAACTGTGGAGATAATACTGATGAAAATGAGTGTGGTAGCTCCTGTACTTTTGAAAAAGGCTGGTGTGGCTGGCAAAACTCCCAGGCTGACAACTTTGATTGGGTTTTAGGGGTTGGCTCTCATCAAAGCTTAAGACCTCCCAAAGACCACACACTTGGAAATGAAAATGGTAGGTTATTAGATTGTTGTAATTGCTTTCACATGATTTTCACAATGTACATCAAAATGTCTTTTC... |
Task1_train_39928 | Chromosome 10 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | ATAAACCTTATGTTCTTACTGGATTAAATTTTCTTTTCTTATGGCTGCATTATTTTCCACGGCCTTCATAGGATCTTTCAGTTTCTCATGCTTTAGTTAGGTCTTTACATCTCTGTTTGTCAGTCTTTTACTAGCAAAATAAATATTCTAGTTTTTTCATATGCCATAATCTGCTGGCCAGGTTATTTTCAACTTTTATTGTGAGCACCAATGTTCCATCCATTCTTTTATCATCAAATATAGAATATGTGAGATATCTTTCATTTCATGTATTTGACAACCAGGTGAATAGTTTTTGCCTTTATCATTACCATTTTGGC... | ATAAACCTTATGTTCTTACTGGATTAAATTTTCTTTTCTTATGGCTGCATTATTTTCCACGGCCTTCATAGGATCTTTCAGTTTCTCATGCTTTAGTTAGGTCTTTACATCTCTGTTTGTCAGTCTTTTACTAGCAAAATAAATATTCTAGTTTTTTCATATGCCATAATCTGCTGGCCAGGTTATTTTCAACTTTTATTGTGAGCACCAATGTTCCATCCATTCTTTTATCATCAAATATAGAATATGTGAGATATCTTTCATTTCATGTATTTGACAACCAGGTGAATAGTTTTTGCCTTTATCATTACCATTTTGGC... |
Task1_train_39929 | A variant found on Chromosome 10 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | TTTCAGTTTCTCATGCTTTAGTTAGGTCTTTACATCTCTGTTTGTCAGTCTTTTACTAGCAAAATAAATATTCTAGTTTTTTCATATGCCATAATCTGCTGGCCAGGTTATTTTCAACTTTTATTGTGAGCACCAATGTTCCATCCATTCTTTTATCATCAAATATAGAATATGTGAGATATCTTTCATTTCATGTATTTGACAACCAGGTGAATAGTTTTTGCCTTTATCATTACCATTTTGGCTGAATAAAAAATATAAAATGGCTAAACACATGCAAAACAGTCTTTCATTAAAAAAATCTATCTTTTCAATTTGCT... | TTTCAGTTTCTCATGCTTTAGTTAGGTCTTTACATCTCTGTTTGTCAGTCTTTTACTAGCAAAATAAATATTCTAGTTTTTTCATATGCCATAATCTGCTGGCCAGGTTATTTTCAACTTTTATTGTGAGCACCAATGTTCCATCCATTCTTTTATCATCAAATATAGAATATGTGAGATATCTTTCATTTCATGTATTTGACAACCAGGTGAATAGTTTTTGCCTTTATCATTACCATTTTGGCTGAATAAAAAATATAAAATGGCTAAACACATGCAAAACAGTCTTTCATTAAAAAAATCTATCTTTTCAATTTGCT... |
Task1_train_39930 | Here’s a variant located on Chromosome 10. What is the predicted biological effect — harmless or disease-causing? | Benign | ATAATCTGCTGGCCAGGTTATTTTCAACTTTTATTGTGAGCACCAATGTTCCATCCATTCTTTTATCATCAAATATAGAATATGTGAGATATCTTTCATTTCATGTATTTGACAACCAGGTGAATAGTTTTTGCCTTTATCATTACCATTTTGGCTGAATAAAAAATATAAAATGGCTAAACACATGCAAAACAGTCTTTCATTAAAAAAATCTATCTTTTCAATTTGCTGTATTCTTAAAAAATATACGTGAGGCTGTTTTTTATTTGTTTATTTTTCTTTGGACACCTAATATTTCATAGATATTCTAGTCATTGTTC... | ATAATCTGCTGGCCAGGTTATTTTCAACTTTTATTGTGAGCACCAATGTTCCATCCATTCTTTTATCATCAAATATAGAATATGTGAGATATCTTTCATTTCATGTATTTGACAACCAGGTGAATAGTTTTTGCCTTTATCATTACCATTTTGGCTGAATAAAAAATATAAAATGGCTAAACACATGCAAAACAGTCTTTCATTAAAAAAATCTATCTTTTCAATTTGCTGTATTCTTAAAAAATATACGTGAGGCTGTTTTTTATTTGTTTATTTTTCTTTGGACACCTAATATTTCATAGATATTCTAGTCATTGTTC... |
Task1_train_39931 | A change on Chromosome 10 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CTGCTTCTGAATGACTTTTGGGTAAATAATGACACTAAAGTAGAAATCAAGACATTTTTTGAAACTAATGAGAACAGGCATACAACATATCAGAATCTCTGGGACACAGCTAAGACACTGTTAAGAGGGAAATTTATAGCACCAAATGCCCACATCAAAAAGTTGGAAAGATCTCAAGTTAACAACCTCAAATAATCTCAAATTAACCATTGCAGTTATTGATTGGTGGGACATCTGCATAAAAGTGTGAAAGGCCATGGAAAGGGATGACTAAGGCCAATACAGAGTGAGAAATATAAGCAAGCAAATATATGTGAATA... | CTGCTTCTGAATGACTTTTGGGTAAATAATGACACTAAAGTAGAAATCAAGACATTTTTTGAAACTAATGAGAACAGGCATACAACATATCAGAATCTCTGGGACACAGCTAAGACACTGTTAAGAGGGAAATTTATAGCACCAAATGCCCACATCAAAAAGTTGGAAAGATCTCAAGTTAACAACCTCAAATAATCTCAAATTAACCATTGCAGTTATTGATTGGTGGGACATCTGCATAAAAGTGTGAAAGGCCATGGAAAGGGATGACTAAGGCCAATACAGAGTGAGAAATATAAGCAAGCAAATATATGTGAATA... |
Task1_train_39932 | Consider a variant on Chromosome 10. Determine its clinical classification and disease relevance. | Benign | AGAAATGCCCAATTATATTATAAGAAGTGGGAGGGAATAATTGAAAATACTCTGTTTTACAGTACTTGTACTACCCATGAAATGGGTTAGTTATGTTGTTACATAAGTTGCTTATAAAATGGTATGATGATATTTGACAGAGGATTTGGCTTGGTAGTTATAATGTATATTGCAAATTCAAAGTCAGTCCCTAGAAAAAGAATGTAAAAACAGAAGATATAAAATTGATATGTTAAGAGAGGATAAAAACAGAATCGTGAAAAGTTCAATTAAAAAACCAGAGAAGACAGAAAAAAACAGGAGGGGGGGGGAGAAAACAA... | AGAAATGCCCAATTATATTATAAGAAGTGGGAGGGAATAATTGAAAATACTCTGTTTTACAGTACTTGTACTACCCATGAAATGGGTTAGTTATGTTGTTACATAAGTTGCTTATAAAATGGTATGATGATATTTGACAGAGGATTTGGCTTGGTAGTTATAATGTATATTGCAAATTCAAAGTCAGTCCCTAGAAAAAGAATGTAAAAACAGAAGATATAAAATTGATATGTTAAGAGAGGATAAAAACAGAATCGTGAAAAGTTCAATTAAAAAACCAGAGAAGACAGAAAAAAACAGGAGGGGGGGGGAGAAAACAA... |
Task1_train_39933 | A mutation on Chromosome 10 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CTACAAACATAGGCTCCCTAAGCACAGCCACATATATCTCAGATACATGGCTTTGGTCATAGGGTCAGAGTCTAAATACCTTCTAGATACATCTTCACTATTGGTTTAGTGAGGAGGGAGAGGGACTTTCACATCTCATTTTTTAAATGAATTTGCTATATCATCTTTACATATAACACAAATTATTCTCATACAACCCATAAATAAAAGTAGTTTAAAATGTCAAGAAAACAAACCATTCCTGTACTGGCCTCCATTGCTACTTGGCTCTATATTTTCCCTTAATATATTGATGAGTCCCTCGTTAACTAGCACAGAGA... | CTACAAACATAGGCTCCCTAAGCACAGCCACATATATCTCAGATACATGGCTTTGGTCATAGGGTCAGAGTCTAAATACCTTCTAGATACATCTTCACTATTGGTTTAGTGAGGAGGGAGAGGGACTTTCACATCTCATTTTTTAAATGAATTTGCTATATCATCTTTACATATAACACAAATTATTCTCATACAACCCATAAATAAAAGTAGTTTAAAATGTCAAGAAAACAAACCATTCCTGTACTGGCCTCCATTGCTACTTGGCTCTATATTTTCCCTTAATATATTGATGAGTCCCTCGTTAACTAGCACAGAGA... |
Task1_train_39934 | A mutation on Chromosome 10 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TGTCAGGATGCATTGGGGAGAAGAGGGAGGCAGTCCCTCTTCTGGGACTGCCTCCCTTTGCAAACTGGAATTTGGGTTTGCAAAATAAGATTAGGCATGCTTGTGTACCTTTAAGTGTTGTTGATAAGAAGCCAGCAGAGAATTAGGGGTGGCAAATATTGTAGAGAAAGGACTATGATCACCTAAGCAAATTCACAATACCTGTGAAGGTGGGCTGAGTTGAGCTAGGACATAGGTAGAAATAGGTTGAAAGGATGGCTATAAGGAAAGGTCCCCATCCATTATCACAGAAGGAAAGAATAGGTCAGCCCAGAGTCAAG... | TGTCAGGATGCATTGGGGAGAAGAGGGAGGCAGTCCCTCTTCTGGGACTGCCTCCCTTTGCAAACTGGAATTTGGGTTTGCAAAATAAGATTAGGCATGCTTGTGTACCTTTAAGTGTTGTTGATAAGAAGCCAGCAGAGAATTAGGGGTGGCAAATATTGTAGAGAAAGGACTATGATCACCTAAGCAAATTCACAATACCTGTGAAGGTGGGCTGAGTTGAGCTAGGACATAGGTAGAAATAGGTTGAAAGGATGGCTATAAGGAAAGGTCCCCATCCATTATCACAGAAGGAAAGAATAGGTCAGCCCAGAGTCAAG... |
Task1_train_39935 | Located on Chromosome 10, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | CCAGGAAATCAAAGCTGCAGGGAACAGTGACTGTGCCACTGCATTCTAGCCTGGGTAATAGAGTGAGGCCTGGTCTAGGAAAAAAAAAAATTTCCTCCCTTCCCATATTAGTTCTTGAATTTAGGAGCCAAAAGGCCTTTGATACTGTGTACCCCATAAGCTTCTCTAGACCATCTTCCTGCCTCGGCAGCTGGGTATAATCTCTTTCTCTTCTGAAACTCTATCTGCAGGGATACACCCCTACCTTTCTCTGGCATTCATCTTTCTGTTTTGCATTAGAGTCCAGTATGCGCATGATTTATTCTGCCCTGCAAGACTTG... | CCAGGAAATCAAAGCTGCAGGGAACAGTGACTGTGCCACTGCATTCTAGCCTGGGTAATAGAGTGAGGCCTGGTCTAGGAAAAAAAAAAATTTCCTCCCTTCCCATATTAGTTCTTGAATTTAGGAGCCAAAAGGCCTTTGATACTGTGTACCCCATAAGCTTCTCTAGACCATCTTCCTGCCTCGGCAGCTGGGTATAATCTCTTTCTCTTCTGAAACTCTATCTGCAGGGATACACCCCTACCTTTCTCTGGCATTCATCTTTCTGTTTTGCATTAGAGTCCAGTATGCGCATGATTTATTCTGCCCTGCAAGACTTG... |
Task1_train_39936 | Assess the clinical impact of this variant found on Chromosome 10. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CTTTATCAGATTCCTCTTCATTGGCTTAAGAAGATACAAGACAGGAGTCTCCAATCCTTAGACCATGGACCAATATCAACCATGGCCAGTTAGCAACCCGGTAACAAAGCAGGAGGTGAGCAAGGGTGAGGGAGCATTCCTGCCTGAGCTCTGCCTCCTGTCAGATCAGCGGTGGCATTAGATTCTCATAGAAGCACAAACCCTATTATGAACTGTGCATGCAAGGGATCTAGGCTGTGCACTCCTTATGAGAATCTAACTAAAGCCTGATGATCTGAGATGGAAGAGTTTCATCCTAAAACCATCCCCTCCAACACCAC... | CTTTATCAGATTCCTCTTCATTGGCTTAAGAAGATACAAGACAGGAGTCTCCAATCCTTAGACCATGGACCAATATCAACCATGGCCAGTTAGCAACCCGGTAACAAAGCAGGAGGTGAGCAAGGGTGAGGGAGCATTCCTGCCTGAGCTCTGCCTCCTGTCAGATCAGCGGTGGCATTAGATTCTCATAGAAGCACAAACCCTATTATGAACTGTGCATGCAAGGGATCTAGGCTGTGCACTCCTTATGAGAATCTAACTAAAGCCTGATGATCTGAGATGGAAGAGTTTCATCCTAAAACCATCCCCTCCAACACCAC... |
Task1_train_39937 | A variant was discovered on Chromosome 10. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CTTTTTAAATCTGGGAATTGACTAGTTTTTAATCTGAGTGATCTATTGTTAGAAGAAAAAAAAAATCTTTGCAAGTTGTTGAATCTTTTAAAAGTCCTAAGGGGAACGTGTTTACTGTCTGTGACAGTGGTTCTTAACAATGTCAGATTTAACAACTTTTTTATAATGAATATGCTGTAATGACTCCCTTTGATAGCCTATTTTATCTACCGAGTGAAATAAACCATCCTAAACAGCATGTATGGCTTCTCATGATTCTGTGGGTTGACTAGGCAGTTCTGCTTGACAAAGTAGAGGCAGTTGGGGCTCTGGGGCCCCTA... | CTTTTTAAATCTGGGAATTGACTAGTTTTTAATCTGAGTGATCTATTGTTAGAAGAAAAAAAAAATCTTTGCAAGTTGTTGAATCTTTTAAAAGTCCTAAGGGGAACGTGTTTACTGTCTGTGACAGTGGTTCTTAACAATGTCAGATTTAACAACTTTTTTATAATGAATATGCTGTAATGACTCCCTTTGATAGCCTATTTTATCTACCGAGTGAAATAAACCATCCTAAACAGCATGTATGGCTTCTCATGATTCTGTGGGTTGACTAGGCAGTTCTGCTTGACAAAGTAGAGGCAGTTGGGGCTCTGGGGCCCCTA... |
Task1_train_39938 | Assess the clinical impact of this variant found on Chromosome 10. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | ATGGCTTCTCATGATTCTGTGGGTTGACTAGGCAGTTCTGCTTGACAAAGTAGAGGCAGTTGGGGCTCTGGGGCCCCTAAGAAGTCAAACTGGCCTCACTCACATAACTCAGCTGGCACTGGCTGCTGGCCTGGAGCTCAGCTGGGGATGCTGGCCTAGGACGACCCTTCTCTTACAGGTTAAACTCTCATGTGGCTTCTCGGGCTTCCTGGTAGCATGGCAGCAAGGTTCAAAGAAAGAGCATTCCTGGAAGCGAAGGTGGAAGCTGCAAGCCTCTTAAGGCCAAGCCCCAAACTTACACACCATTATTTCGCTGCATT... | ATGGCTTCTCATGATTCTGTGGGTTGACTAGGCAGTTCTGCTTGACAAAGTAGAGGCAGTTGGGGCTCTGGGGCCCCTAAGAAGTCAAACTGGCCTCACTCACATAACTCAGCTGGCACTGGCTGCTGGCCTGGAGCTCAGCTGGGGATGCTGGCCTAGGACGACCCTTCTCTTACAGGTTAAACTCTCATGTGGCTTCTCGGGCTTCCTGGTAGCATGGCAGCAAGGTTCAAAGAAAGAGCATTCCTGGAAGCGAAGGTGGAAGCTGCAAGCCTCTTAAGGCCAAGCCCCAAACTTACACACCATTATTTCGCTGCATT... |
Task1_train_39939 | A mutation on Chromosome 10 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GTGGGTTGACTAGGCAGTTCTGCTTGACAAAGTAGAGGCAGTTGGGGCTCTGGGGCCCCTAAGAAGTCAAACTGGCCTCACTCACATAACTCAGCTGGCACTGGCTGCTGGCCTGGAGCTCAGCTGGGGATGCTGGCCTAGGACGACCCTTCTCTTACAGGTTAAACTCTCATGTGGCTTCTCGGGCTTCCTGGTAGCATGGCAGCAAGGTTCAAAGAAAGAGCATTCCTGGAAGCGAAGGTGGAAGCTGCAAGCCTCTTAAGGCCAAGCCCCAAACTTACACACCATTATTTCGCTGCATTCTATTGGCCAAAACAGGT... | GTGGGTTGACTAGGCAGTTCTGCTTGACAAAGTAGAGGCAGTTGGGGCTCTGGGGCCCCTAAGAAGTCAAACTGGCCTCACTCACATAACTCAGCTGGCACTGGCTGCTGGCCTGGAGCTCAGCTGGGGATGCTGGCCTAGGACGACCCTTCTCTTACAGGTTAAACTCTCATGTGGCTTCTCGGGCTTCCTGGTAGCATGGCAGCAAGGTTCAAAGAAAGAGCATTCCTGGAAGCGAAGGTGGAAGCTGCAAGCCTCTTAAGGCCAAGCCCCAAACTTACACACCATTATTTCGCTGCATTCTATTGGCCAAAACAGGT... |
Task1_train_39940 | An alteration has been detected on Chromosome 10. Is it pathogenic, and if so, what disease is involved? | Benign | ACCACTCACAACTGAGGAAAACTAAACATTCCTTAATGAAAGACTGGAGGAAAATGTTAGAAGAGAAAAGCAAACACTTGTATCGTTTTGTTTGTTTGAAGTAGATGCTTACAGGCTAAGCACAGTGGCTCATGCCTGTAATCACAGCACTTTGGGAGGCTGAGGTGGGAGGATTGCTTGAGGCCAGGAGTTCAAGACCAGCCTGCGCAACAAAGCAAGACCCTAGTCTCTACAAAAAAAAAAAAATTCAAAAATTAGCCAGGCACCGTGGTGCATGCCTGTAGTCCCAGCTACTATGGAGGCTGAGGCGGGAGGACTGC... | ACCACTCACAACTGAGGAAAACTAAACATTCCTTAATGAAAGACTGGAGGAAAATGTTAGAAGAGAAAAGCAAACACTTGTATCGTTTTGTTTGTTTGAAGTAGATGCTTACAGGCTAAGCACAGTGGCTCATGCCTGTAATCACAGCACTTTGGGAGGCTGAGGTGGGAGGATTGCTTGAGGCCAGGAGTTCAAGACCAGCCTGCGCAACAAAGCAAGACCCTAGTCTCTACAAAAAAAAAAAAATTCAAAAATTAGCCAGGCACCGTGGTGCATGCCTGTAGTCCCAGCTACTATGGAGGCTGAGGCGGGAGGACTGC... |
Task1_train_39941 | Assess the clinical impact of this variant found on Chromosome 10. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | ACTCTGAATGGAACAGGAACCGTGGCAGTGTCCTGGGCAGAAGAATGACAGGATTGGTCTTATTTTAAAAGGCTCTCTTTTGCCTTCTTCCCAAAGGACCATGAAATGTATCTTGGATGAGAAAGGGATTCAACTATAACTTAATTGGAAAAAGATCTCAAAAGTGATCTAGTCTAGCCCTCTTCCTCCAGGCTTGTGAAACTGCCTGCACAGGGCTTTGTCTAGCCTACTTTTAGATACACTCACAACACTTTTAGTCATCTGTTCCAGTATTCAGTTACTTTTGCAGGCAGTCAGCTCTCCCTTAGGTATATAGATGG... | ACTCTGAATGGAACAGGAACCGTGGCAGTGTCCTGGGCAGAAGAATGACAGGATTGGTCTTATTTTAAAAGGCTCTCTTTTGCCTTCTTCCCAAAGGACCATGAAATGTATCTTGGATGAGAAAGGGATTCAACTATAACTTAATTGGAAAAAGATCTCAAAAGTGATCTAGTCTAGCCCTCTTCCTCCAGGCTTGTGAAACTGCCTGCACAGGGCTTTGTCTAGCCTACTTTTAGATACACTCACAACACTTTTAGTCATCTGTTCCAGTATTCAGTTACTTTTGCAGGCAGTCAGCTCTCCCTTAGGTATATAGATGG... |
Task1_train_39942 | Consider this mutation on Chromosome 10. Is this a benign change or a disease-causing variant? | Benign | TTTCTAGGGGCTTTTCCAACCACACTTGAGACCACTTGAGGCCACATCCTCTTATACTCCAATCAAAACAACATAGCAACAGACTGAATTCAGAGGCACATATGAAGATTCAGTTGTCTTTTTTTTAAGCCGGATGTTAAAGAGCCTTGCAAAATTGTAAAACAGTGCAACTCTTCTCATGAAATGTTTGTTTCATTTTGAAAAGTATAATTATTTGCCTTAAATATATGTTATGTTAACATATAATAAATTTATTTCAGGTTGAGCATCTCTACTCTGAAAATTCGAAATCTGAAATGCACCCAAATCTGAAACTTTTT... | TTTCTAGGGGCTTTTCCAACCACACTTGAGACCACTTGAGGCCACATCCTCTTATACTCCAATCAAAACAACATAGCAACAGACTGAATTCAGAGGCACATATGAAGATTCAGTTGTCTTTTTTTTAAGCCGGATGTTAAAGAGCCTTGCAAAATTGTAAAACAGTGCAACTCTTCTCATGAAATGTTTGTTTCATTTTGAAAAGTATAATTATTTGCCTTAAATATATGTTATGTTAACATATAATAAATTTATTTCAGGTTGAGCATCTCTACTCTGAAAATTCGAAATCTGAAATGCACCCAAATCTGAAACTTTTT... |
Task1_train_39943 | This sequence change occurs on Chromosome 10. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | CGCTCCTGGCCTTAAATTTTGTGATTTTTAAACAAGAGTATTGATTATGTATATCTAGTCTTTACATCTATTCTTACATATGTCTACAGCTCAAACACTCTGCTAAGGTCAACACACATTTATTCTACTAGGGCCCTTAAGTGTTACTAGGCATTACGTATCCAACAGATCCAAACAGAGTTCAACACCTTCACTGTCATCCTTTCTGCGTCCCCTTATTAACAGCAGCATAAGCCAGAAACCCATTTTAAGCCCCTTCTTCTCTTTCACGAACTAATCAAACTTGTTCGATCTACCCCTAATTCTGTACCAAACCTCGT... | CGCTCCTGGCCTTAAATTTTGTGATTTTTAAACAAGAGTATTGATTATGTATATCTAGTCTTTACATCTATTCTTACATATGTCTACAGCTCAAACACTCTGCTAAGGTCAACACACATTTATTCTACTAGGGCCCTTAAGTGTTACTAGGCATTACGTATCCAACAGATCCAAACAGAGTTCAACACCTTCACTGTCATCCTTTCTGCGTCCCCTTATTAACAGCAGCATAAGCCAGAAACCCATTTTAAGCCCCTTCTTCTCTTTCACGAACTAATCAAACTTGTTCGATCTACCCCTAATTCTGTACCAAACCTCGT... |
Task1_train_39944 | A mutation on Chromosome 10 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TTTTCTACTTACCTACCACTACGATGACCCTGAACAAGAAACAGAGATTTGATTTTGATTTTCTTCAAGGATTATTACCTTCTGCAATGGAAAATGACAACTCATCAAATGTATGGTTTCTGCCGTGAGCTATAAAGATGACCAAAAGGCAGAGGTTATAAATGTAGCCATGTTGCTTAAAGTAATATTATTTCTTGGCTATCTTGCTAAACTGAATCTACCTTCTTTAAAAAAAAATGTCAGGAATGAGGACATCATACCTTGATATTCTGCTGAGCACAGTAAGGAGGAAGCTACTTCACTGAGGACCACGTGAATTT... | TTTTCTACTTACCTACCACTACGATGACCCTGAACAAGAAACAGAGATTTGATTTTGATTTTCTTCAAGGATTATTACCTTCTGCAATGGAAAATGACAACTCATCAAATGTATGGTTTCTGCCGTGAGCTATAAAGATGACCAAAAGGCAGAGGTTATAAATGTAGCCATGTTGCTTAAAGTAATATTATTTCTTGGCTATCTTGCTAAACTGAATCTACCTTCTTTAAAAAAAAATGTCAGGAATGAGGACATCATACCTTGATATTCTGCTGAGCACAGTAAGGAGGAAGCTACTTCACTGAGGACCACGTGAATTT... |
Task1_train_39945 | This mutation on Chromosome 10 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GACCTCCTGAAGGAGTATCTGTGAGACTGTTGGTCCCACCTAGAAAAGAGGAACAAAGCATTTTGAGTGGCCTGGGCCAGGCTTCCTTACCAAAGGTAAACCTGCTCACCGAAGAGGTCACAGTGGAGTAAAGACCAAAAGACATTCAGGAATTTCACTGCAAAGAAAATTCCAGGACTCCACACTCACTGAAAACACATATGCATGCAAAATTTGTGTTGCCAGAAGTACCTTCACTGGCCAGGCACAGTGGCTCACACCTGTCATCCCCGCACTTTGGGAGCTGAGGTGGGTGGATCACTTGAGGTCAGGAGTTGGAG... | GACCTCCTGAAGGAGTATCTGTGAGACTGTTGGTCCCACCTAGAAAAGAGGAACAAAGCATTTTGAGTGGCCTGGGCCAGGCTTCCTTACCAAAGGTAAACCTGCTCACCGAAGAGGTCACAGTGGAGTAAAGACCAAAAGACATTCAGGAATTTCACTGCAAAGAAAATTCCAGGACTCCACACTCACTGAAAACACATATGCATGCAAAATTTGTGTTGCCAGAAGTACCTTCACTGGCCAGGCACAGTGGCTCACACCTGTCATCCCCGCACTTTGGGAGCTGAGGTGGGTGGATCACTTGAGGTCAGGAGTTGGAG... |
Task1_train_39946 | A variant was discovered on Chromosome 10. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CATGGCACTTGTTTGGGGGCTTCCTGGGGAGCAAGCAGAAGTAAAACAGGAGGTATTTGGTGGCTCGTGTACCTTGTACTTTGCACAGTATTTGCGTGTGATTAATTCTGACTGCGTTGTTTGTGTGTCATTCCTCAGGCGTGTATGAACAGTCTTTCCATTCTTAAGTAAGGTCATAGGGGTTGCTCTGGGTTGACTTTGGCTGGGCCCGGGTGTTTGTGCTTTGTGTTGTCATTGCTTTAACCAAGCAGCCTTCATGGGAATTGTGCTCCATCCTGCTATAATCAATCACCTCAGCATGAAGAAAGGGCAGCAGTGCC... | CATGGCACTTGTTTGGGGGCTTCCTGGGGAGCAAGCAGAAGTAAAACAGGAGGTATTTGGTGGCTCGTGTACCTTGTACTTTGCACAGTATTTGCGTGTGATTAATTCTGACTGCGTTGTTTGTGTGTCATTCCTCAGGCGTGTATGAACAGTCTTTCCATTCTTAAGTAAGGTCATAGGGGTTGCTCTGGGTTGACTTTGGCTGGGCCCGGGTGTTTGTGCTTTGTGTTGTCATTGCTTTAACCAAGCAGCCTTCATGGGAATTGTGCTCCATCCTGCTATAATCAATCACCTCAGCATGAAGAAAGGGCAGCAGTGCC... |
Task1_train_39947 | Chromosome 10 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TAGCTTTACAATTGATAGCTTTAAAAATGTTTCCGTAGAAAAGAAACAACAGTCCTCAACAGCTTTAAAAATGTTCCCGTAGAAAAGAAAAACTCAACTAGTACTCAAAGAGAAGCATATTATATTGTAAAATGATGGAGAACTCTTTTCATAAACCCATGGGACACCAGGGGGACTACAAGTATGGCCTTGGTTGGTGGCAAAAAGAGAAGGAAAAAAGCCCCTGCATCGCATGCCTCCAGGGGGCGCTCTTCACAGGCATTCCATATAAATGGCGTGCTCCCTGGAGCTGTGCTCTGGGACGAGGCTGAATGAGGCAA... | TAGCTTTACAATTGATAGCTTTAAAAATGTTTCCGTAGAAAAGAAACAACAGTCCTCAACAGCTTTAAAAATGTTCCCGTAGAAAAGAAAAACTCAACTAGTACTCAAAGAGAAGCATATTATATTGTAAAATGATGGAGAACTCTTTTCATAAACCCATGGGACACCAGGGGGACTACAAGTATGGCCTTGGTTGGTGGCAAAAAGAGAAGGAAAAAAGCCCCTGCATCGCATGCCTCCAGGGGGCGCTCTTCACAGGCATTCCATATAAATGGCGTGCTCCCTGGAGCTGTGCTCTGGGACGAGGCTGAATGAGGCAA... |
Task1_train_39948 | This mutation on Chromosome 10 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TCCCAGCACTTTGGGAGGCTGAGGCAGGTGGATAACAAGGTGATAAGTTCGAGACCAGCCTGACCAACATGGTGAAACCCTGTCTCTACTAAAAACACAAAAATTAGCCAGGCGTGGTGGCGCGTGTCTGTAGTCCCAGCTACTCAGGAAGCCGAGGCAGGAGAATCACTTGAACCTAGGAGGCAGAGATTGCAGTGAGCCGAGATGATGCCACTGCACTCCAGCTTGGGTGACACAGTGAGACTCCATCACAAAAATAAATAAATAAATAAATAACCTCATTTAGTCCCACAGCAATTCATGTTTCATAAATAAGTAAA... | TCCCAGCACTTTGGGAGGCTGAGGCAGGTGGATAACAAGGTGATAAGTTCGAGACCAGCCTGACCAACATGGTGAAACCCTGTCTCTACTAAAAACACAAAAATTAGCCAGGCGTGGTGGCGCGTGTCTGTAGTCCCAGCTACTCAGGAAGCCGAGGCAGGAGAATCACTTGAACCTAGGAGGCAGAGATTGCAGTGAGCCGAGATGATGCCACTGCACTCCAGCTTGGGTGACACAGTGAGACTCCATCACAAAAATAAATAAATAAATAAATAACCTCATTTAGTCCCACAGCAATTCATGTTTCATAAATAAGTAAA... |
Task1_train_39949 | This mutation occurs on Chromosome 10. Does this change lead to a known medical condition, or is it benign? | Benign | GCATCTGAAGGAAGCAGATGTTTTTAGTAGTCAACGGACTATTACCCTCTAAGCCTAATCTAACATCACATGTAACTTTATCAATGGCTGCATGATTCTTCCAATACTACTCAGGGATATGGTTCACCTATAAACAATATGCTGTGTTTTGTTCTGGTCCAGGCTCAGTCTGGTCCTCACAACTTGAATGTACAAAGTGCTTGCTCCTTGATGCAAGGTTAGAATACATGAGTTCGTGTCTTAAAGTCCACACTTTATGTGAAACAAAACACAAAAGAATCAGAAAATACAAATCAGAAAAGTACAAATCAGAAGGTGCT... | GCATCTGAAGGAAGCAGATGTTTTTAGTAGTCAACGGACTATTACCCTCTAAGCCTAATCTAACATCACATGTAACTTTATCAATGGCTGCATGATTCTTCCAATACTACTCAGGGATATGGTTCACCTATAAACAATATGCTGTGTTTTGTTCTGGTCCAGGCTCAGTCTGGTCCTCACAACTTGAATGTACAAAGTGCTTGCTCCTTGATGCAAGGTTAGAATACATGAGTTCGTGTCTTAAAGTCCACACTTTATGTGAAACAAAACACAAAAGAATCAGAAAATACAAATCAGAAAAGTACAAATCAGAAGGTGCT... |
Task1_train_39950 | This sequence variant lies on Chromosome 10. Is it clinically significant, and what condition might it cause if any? | Benign | AAGTCTGGAGTAGTAGTTATCAGTGAATGAGTGGTGTGTAAGGCTATGATATAAGGAAGTGAATGTAGAGAAGAAGATAACTTCAAGAACTGAAACTTGGGAGACCCCCAAAATGTAACAGAAAGATAAGGAAAAAACCGAAAAAGATACTCAGACAGAGATACCAGTGAGTTAAGGAAGAGAATCAAGAGAGACTTACAGGAAACCAAGGCAAAGGTATTCAAGAACGCCTTTGTTAAATGCGCCTGGTAGATTAGGTAAAATGAGGACTTAAAATTGACCATTGGATTTAGCAATGTAAAGGTCAATAGAGTCCTTAA... | AAGTCTGGAGTAGTAGTTATCAGTGAATGAGTGGTGTGTAAGGCTATGATATAAGGAAGTGAATGTAGAGAAGAAGATAACTTCAAGAACTGAAACTTGGGAGACCCCCAAAATGTAACAGAAAGATAAGGAAAAAACCGAAAAAGATACTCAGACAGAGATACCAGTGAGTTAAGGAAGAGAATCAAGAGAGACTTACAGGAAACCAAGGCAAAGGTATTCAAGAACGCCTTTGTTAAATGCGCCTGGTAGATTAGGTAAAATGAGGACTTAAAATTGACCATTGGATTTAGCAATGTAAAGGTCAATAGAGTCCTTAA... |
Task1_train_39951 | This alteration on Chromosome 10 may affect genome function. Does it lead to a disease or is it benign? | Benign | GAACTGAAACTTGGGAGACCCCCAAAATGTAACAGAAAGATAAGGAAAAAACCGAAAAAGATACTCAGACAGAGATACCAGTGAGTTAAGGAAGAGAATCAAGAGAGACTTACAGGAAACCAAGGCAAAGGTATTCAAGAACGCCTTTGTTAAATGCGCCTGGTAGATTAGGTAAAATGAGGACTTAAAATTGACCATTGGATTTAGCAATGTAAAGGTCAATAGAGTCCTTAACAAAAGCTGCTTCCACAGAGTGTCAAGATGAAAGCCTGAAGAAACTAAGTATATGCCGAGCATGGTGGCTCACGCCTATAATCCAA... | GAACTGAAACTTGGGAGACCCCCAAAATGTAACAGAAAGATAAGGAAAAAACCGAAAAAGATACTCAGACAGAGATACCAGTGAGTTAAGGAAGAGAATCAAGAGAGACTTACAGGAAACCAAGGCAAAGGTATTCAAGAACGCCTTTGTTAAATGCGCCTGGTAGATTAGGTAAAATGAGGACTTAAAATTGACCATTGGATTTAGCAATGTAAAGGTCAATAGAGTCCTTAACAAAAGCTGCTTCCACAGAGTGTCAAGATGAAAGCCTGAAGAAACTAAGTATATGCCGAGCATGGTGGCTCACGCCTATAATCCAA... |
Task1_train_39952 | Chromosome 10 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | AGAGTTATTGAATATGAGGATAACTGGCCCCTCTTAGATATGTTTCTGCAAAAGCCAATGGGTTTACTTTCCCTACTTGATGAAGAAAGTAGATTTCCCAAGGCCACTGACCAGACTCTTGTAGGTGAGTTTTCAGTCCAGTGTGTCTGCATGGTTTTATGAATAGAGTCTTGTCATTCTGAATGATTTTTTAAATGGCTTTAAATTATCTGGAAGAAAATAGCTGTCACAAAGCCTGCATATTTGACTTTAAAGAAGAGCCTTTGGATTTAATACCTGGACCAGTGCATGTTTATGATAGGGTAAAATATTTAGTGATA... | AGAGTTATTGAATATGAGGATAACTGGCCCCTCTTAGATATGTTTCTGCAAAAGCCAATGGGTTTACTTTCCCTACTTGATGAAGAAAGTAGATTTCCCAAGGCCACTGACCAGACTCTTGTAGGTGAGTTTTCAGTCCAGTGTGTCTGCATGGTTTTATGAATAGAGTCTTGTCATTCTGAATGATTTTTTAAATGGCTTTAAATTATCTGGAAGAAAATAGCTGTCACAAAGCCTGCATATTTGACTTTAAAGAAGAGCCTTTGGATTTAATACCTGGACCAGTGCATGTTTATGATAGGGTAAAATATTTAGTGATA... |
Task1_train_39953 | This sequence change occurs on Chromosome 10. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TAGGATCAAGGCGACCTTCCTTCCTTGGGCAATGTAGGATAAAAGAAAAAAACCAAGTACTTTTTTTTCCTCTGTGCTCTAGATAACCCTCCCATTATTGGTTCCAGTTCTTGTTTACCTATTCTGATAAAAACCTATTAACCATCCAATGAAAATGAAGAAAATACCACTAAAACTTGGAGTTATTACTTATGTAATTTAATGTGGAGGAGGTGGAGGAAATTAGATTAAATTTACTCTAAGTGTTCAGTGAATGTATCCAACTCTCTAGCAGAAACATAAAATTCTTTAAAAAATATATGAGTACCTTTACTAAATAT... | TAGGATCAAGGCGACCTTCCTTCCTTGGGCAATGTAGGATAAAAGAAAAAAACCAAGTACTTTTTTTTCCTCTGTGCTCTAGATAACCCTCCCATTATTGGTTCCAGTTCTTGTTTACCTATTCTGATAAAAACCTATTAACCATCCAATGAAAATGAAGAAAATACCACTAAAACTTGGAGTTATTACTTATGTAATTTAATGTGGAGGAGGTGGAGGAAATTAGATTAAATTTACTCTAAGTGTTCAGTGAATGTATCCAACTCTCTAGCAGAAACATAAAATTCTTTAAAAAATATATGAGTACCTTTACTAAATAT... |
Task1_train_39954 | A mutation located on Chromosome 10 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GTGGATGACAAAGTCAGACATGAAAGAAGTAGAGGCAGAAAGTCAAGGGAAGCTTGTAGAGAGGAAAGTTAGGGAAGGGAGAAGCAGGTGGGCCTGACCACTGCCAGAGATCTGCGGGCCAGCACTCCCTCCCTCCTCCACTTCTGACTTTCCTTTTCCCTCAGCTACCTGAAGCGCTTGTTTTCACTTAACCATTCCCTGTCAGAGCCCCTGAACTGTGACCTAGAATACCACAGCGGGGAGCTGGAGAAAGGCCCAGGCCGGCAGGGCTCTCCAGCAGATGTCAGAAGAGATCGCCAGTCCTCCCCACGCTGGAGCTC... | GTGGATGACAAAGTCAGACATGAAAGAAGTAGAGGCAGAAAGTCAAGGGAAGCTTGTAGAGAGGAAAGTTAGGGAAGGGAGAAGCAGGTGGGCCTGACCACTGCCAGAGATCTGCGGGCCAGCACTCCCTCCCTCCTCCACTTCTGACTTTCCTTTTCCCTCAGCTACCTGAAGCGCTTGTTTTCACTTAACCATTCCCTGTCAGAGCCCCTGAACTGTGACCTAGAATACCACAGCGGGGAGCTGGAGAAAGGCCCAGGCCGGCAGGGCTCTCCAGCAGATGTCAGAAGAGATCGCCAGTCCTCCCCACGCTGGAGCTC... |
Task1_train_39955 | A variant affecting Chromosome 10 has been observed. Determine if it's benign or associated with disease. | Benign | ATATGTGAAACCCAGTCTCTACTAGAAATATAAAAATTAGCTGGGTGTGGTGGCACACACCTGTAATCCCAGCTATCTGAGAGGCTAAGACACAAGAATTGCCTGAACCTAGACATAGAGGTTGCAGTGAGCCAAGATGGCACCACTGCACTCCAGCCTGGACAACAGAGTAAAACGCTGTCTCAAAAAAACAAACAAAAAAAGAATTACATGAGAAATTTGAAACCCAAAGGAAAAAAGACAACATAACTAACCTTGCTCAAGTAGTTCTCCATGCTATTATTTGAAGCCCGTGGATTTGAGGTAGAGATCACTAAGTT... | ATATGTGAAACCCAGTCTCTACTAGAAATATAAAAATTAGCTGGGTGTGGTGGCACACACCTGTAATCCCAGCTATCTGAGAGGCTAAGACACAAGAATTGCCTGAACCTAGACATAGAGGTTGCAGTGAGCCAAGATGGCACCACTGCACTCCAGCCTGGACAACAGAGTAAAACGCTGTCTCAAAAAAACAAACAAAAAAAGAATTACATGAGAAATTTGAAACCCAAAGGAAAAAAGACAACATAACTAACCTTGCTCAAGTAGTTCTCCATGCTATTATTTGAAGCCCGTGGATTTGAGGTAGAGATCACTAAGTT... |
Task1_train_39956 | This variant lies on Chromosome 10. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | TGTAACCTCCACCTTCTGGGTTCAAGCAATTCTCCTACTTCAGCCTCCTGAGTAGTAGGATTACAGGGGCCTGCCATCACGCCTGGCTAATTTTTGTATTTACAGTAGAGACAGGGTTTTGCCATGTTGGCCAGGCTGGTCTCAAACTCCTAACCTCAGGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGCATGAGCCACTGCGCCTGACAGGAACTGTTAAGGTTTTGAAAGACTGATGAACACAGATAAATGGGAAAAAAAGTTTCTGAATCTGCAATGCTAGGAGCACTGTGTTATTCTGTAATGTCCTGCTG... | TGTAACCTCCACCTTCTGGGTTCAAGCAATTCTCCTACTTCAGCCTCCTGAGTAGTAGGATTACAGGGGCCTGCCATCACGCCTGGCTAATTTTTGTATTTACAGTAGAGACAGGGTTTTGCCATGTTGGCCAGGCTGGTCTCAAACTCCTAACCTCAGGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGCATGAGCCACTGCGCCTGACAGGAACTGTTAAGGTTTTGAAAGACTGATGAACACAGATAAATGGGAAAAAAAGTTTCTGAATCTGCAATGCTAGGAGCACTGTGTTATTCTGTAATGTCCTGCTG... |
Task1_train_39957 | A mutation has occurred on Chromosome 10. What is the medical relevance of this mutation? | Benign | TACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCAGAGCTGAGATCGCACCACTGCACTCCAGCCTGGGCGACAGAGTGAGACTCCATCTCAAAAAAAAAAAAAAAAAAAAATTACATAAAAGTAACTTCAGGCTACATATATAAGGTATATATGAAAAATCAATGAATTTCATGTTAGGCTTGGGTCCTGTCTCCAAGATATCTCATTATGTATGTACAAATATTCCAAAATAAAAAAAAATCCAAAATCTGAAACACTTCTGGTCTCAAGCATTTTAAATAAGGGATACTCAACTTGTCCTACTAAAG... | TACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCAGAGCTGAGATCGCACCACTGCACTCCAGCCTGGGCGACAGAGTGAGACTCCATCTCAAAAAAAAAAAAAAAAAAAAATTACATAAAAGTAACTTCAGGCTACATATATAAGGTATATATGAAAAATCAATGAATTTCATGTTAGGCTTGGGTCCTGTCTCCAAGATATCTCATTATGTATGTACAAATATTCCAAAATAAAAAAAAATCCAAAATCTGAAACACTTCTGGTCTCAAGCATTTTAAATAAGGGATACTCAACTTGTCCTACTAAAG... |
Task1_train_39958 | Chromosome 10 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCAGAGCTGAGATCGCACCACTGCACTCCAGCCTGGGCGACAGAGTGAGACTCCATCTCAAAAAAAAAAAAAAAAAAAAATTACATAAAAGTAACTTCAGGCTACATATATAAGGTATATATGAAAAATCAATGAATTTCATGTTAGGCTTGGGTCCTGTCTCCAAGATATCTCATTATGTATGTACAAATATTCCAAAATAAAAAAAAATCCAAAATCTGAAACACTTCTGGTCTCAAGCATTTTAAATAAGGGATACTCAACTTGTCCTACTAAAGCAA... | TCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCAGAGCTGAGATCGCACCACTGCACTCCAGCCTGGGCGACAGAGTGAGACTCCATCTCAAAAAAAAAAAAAAAAAAAAATTACATAAAAGTAACTTCAGGCTACATATATAAGGTATATATGAAAAATCAATGAATTTCATGTTAGGCTTGGGTCCTGTCTCCAAGATATCTCATTATGTATGTACAAATATTCCAAAATAAAAAAAAATCCAAAATCTGAAACACTTCTGGTCTCAAGCATTTTAAATAAGGGATACTCAACTTGTCCTACTAAAGCAA... |
Task1_train_39959 | A sequence alteration has been identified on Chromosome 10. Is it disease-inducing or harmless? | Benign | CTTCATGACTATGAGAATTCTAAGTAAAACAAAGGAAACTTTGAGCTAGCACCCAAGAAAATGACAGATCATGATTTCCTCTGAAATTAAAGAATAAACTGTACATTTTACAATAAAGGGTTGCAATAAGTGTATATCCAATTGAAAAAAAAAAAGTTGGATCAAAACTCAAACCGTATAGAGCATAAACTCCCAAAAGTTCAAAAATTTATTTGAAGACAATTAATCCATGAAAGTAAAAAAGAAACCACTAGAAAATTTTTAAGAATCACAGAATTGGAAAGGCCTTTTACTGAAGTACAACAAATTCAAAAGCATAA... | CTTCATGACTATGAGAATTCTAAGTAAAACAAAGGAAACTTTGAGCTAGCACCCAAGAAAATGACAGATCATGATTTCCTCTGAAATTAAAGAATAAACTGTACATTTTACAATAAAGGGTTGCAATAAGTGTATATCCAATTGAAAAAAAAAAAGTTGGATCAAAACTCAAACCGTATAGAGCATAAACTCCCAAAAGTTCAAAAATTTATTTGAAGACAATTAATCCATGAAAGTAAAAAAGAAACCACTAGAAAATTTTTAAGAATCACAGAATTGGAAAGGCCTTTTACTGAAGTACAACAAATTCAAAAGCATAA... |
Task1_train_39960 | A variant found on Chromosome 10 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | AGGCTAGTTTCGAACTCCTGGGTCAAGCAATCCTCCTGCCTGGGCCTCCCAAAGTGCTGGGATTACAGTCATGAGCCACAGGTGCCCAGCCAAGATCCCCTTTACTTCTGAAAAGGATAAAAGTTGTCAGACGATAGCAATCCACCAAAAAAAGAAAAAAAAGAAAGTGGGAAATGATTTTTATCTGTGCAAGATTCATATTCCTCTCTTCCCAAGGATTACTTCATTAATAATAAATTTTCACTAGAACTTTTATACATACTCATTGCAGAAATCATAAAGAAAAAAGTTTGACTTATTATACAAATGCCCAGAAATAA... | AGGCTAGTTTCGAACTCCTGGGTCAAGCAATCCTCCTGCCTGGGCCTCCCAAAGTGCTGGGATTACAGTCATGAGCCACAGGTGCCCAGCCAAGATCCCCTTTACTTCTGAAAAGGATAAAAGTTGTCAGACGATAGCAATCCACCAAAAAAAGAAAAAAAAGAAAGTGGGAAATGATTTTTATCTGTGCAAGATTCATATTCCTCTCTTCCCAAGGATTACTTCATTAATAATAAATTTTCACTAGAACTTTTATACATACTCATTGCAGAAATCATAAAGAAAAAAGTTTGACTTATTATACAAATGCCCAGAAATAA... |
Task1_train_39961 | A sequence alteration has been identified on Chromosome 10. Is it disease-inducing or harmless? | Benign | GGCTGTAAAAGATTGGGTCAACCAGGTATGCATTAATATTATCAAGATATTTAACCTAAGGAGTACATATTATCAGTTAAAACAATCAGATTTTAAAAGTCTAACAAATATATTTCCTTTTTTTAATATTTAAAAATAAATTGATGCAAATATTTTCACAGTTCGTTTTACTGAGATCAGTCATATGAGGTTTGACATAGGTTAAAAAATTATATTCCTAATGGTATCCTTAAATAAAGAGATGACATTTCAGCATGAATGAGAAAAACTTTTTTTTTTTTTAAATCAAACCCAAACCACTACTGTCCTAAGCATTATGG... | GGCTGTAAAAGATTGGGTCAACCAGGTATGCATTAATATTATCAAGATATTTAACCTAAGGAGTACATATTATCAGTTAAAACAATCAGATTTTAAAAGTCTAACAAATATATTTCCTTTTTTTAATATTTAAAAATAAATTGATGCAAATATTTTCACAGTTCGTTTTACTGAGATCAGTCATATGAGGTTTGACATAGGTTAAAAAATTATATTCCTAATGGTATCCTTAAATAAAGAGATGACATTTCAGCATGAATGAGAAAAACTTTTTTTTTTTTTAAATCAAACCCAAACCACTACTGTCCTAAGCATTATGG... |
Task1_train_39962 | Here is a mutation located on Chromosome 10. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | ATCATGCCTCCAGACTGGGCAACGAGCAAAACTCCATCTTCAAAAAAAAATATCCTTTTTGCTTGAGACTAAATGCTCATTATTATTACTAAGTTAATGATAGTTAATAAAGTTTACTATTCATTTACACATCAAAAATAAGCACTATTAGAGTTTACTGAAGACTCACTCTACTTGACTAATCTTGTAAAAATCTTGATCACCAAGCACCAATTTGCAATATTATATACAAAGCTGAGTACCCACAAATACCCACAGATAGTTGGAATTCAGAAAAAAAAATCATTATTAATGCATTATCAGTTCATCTTGTTGACAAT... | ATCATGCCTCCAGACTGGGCAACGAGCAAAACTCCATCTTCAAAAAAAAATATCCTTTTTGCTTGAGACTAAATGCTCATTATTATTACTAAGTTAATGATAGTTAATAAAGTTTACTATTCATTTACACATCAAAAATAAGCACTATTAGAGTTTACTGAAGACTCACTCTACTTGACTAATCTTGTAAAAATCTTGATCACCAAGCACCAATTTGCAATATTATATACAAAGCTGAGTACCCACAAATACCCACAGATAGTTGGAATTCAGAAAAAAAAATCATTATTAATGCATTATCAGTTCATCTTGTTGACAAT... |
Task1_train_39963 | A mutation found on Chromosome 10 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CACAGTGAAAAAAGTAAATGTCTAAGAAAATACATCAAAAGAATTTTAGCAGAATTTCAATATCACTAAAGATATTGAATATATGTAAAATATTCTTTAAAAAAAAAAAAACATAGAGCATGCCAGGCTCAGTGGCTCACGCCTATAATCCCAAGCACTCTGGGAGGCTGAGGTGGGCTGATTACTTGAGCTCAGGAGTTTGAGACCAGCCTGGGCAACATGGCAAAACTCTGTTTCTACAAAAAGTACAAAAATTAGCCAGATGTGGTGGTGTGCACCTGTAGTTCCAGCTACTTGGGAGGCTGAGGTGGGAGGATGAC... | CACAGTGAAAAAAGTAAATGTCTAAGAAAATACATCAAAAGAATTTTAGCAGAATTTCAATATCACTAAAGATATTGAATATATGTAAAATATTCTTTAAAAAAAAAAAAACATAGAGCATGCCAGGCTCAGTGGCTCACGCCTATAATCCCAAGCACTCTGGGAGGCTGAGGTGGGCTGATTACTTGAGCTCAGGAGTTTGAGACCAGCCTGGGCAACATGGCAAAACTCTGTTTCTACAAAAAGTACAAAAATTAGCCAGATGTGGTGGTGTGCACCTGTAGTTCCAGCTACTTGGGAGGCTGAGGTGGGAGGATGAC... |
Task1_train_39964 | This mutation occurs on Chromosome 10. Does this change lead to a known medical condition, or is it benign? | Benign | GAGCTGGAGCCACTGATTGCAAAACAGCAAAAACATGGCTAAAGCCTTTAGGCAAGGTCACATTTAAATAGCCAGCGTTTCTAATCATTAATACAACTTCTACACTGTTGCTGTTTTTCACTTTTCCCAACCCATTGGTTGGTGTGATGAGTTAAATTCAAGGCCCAAAACCAACAAGTTCCAGGGTAAAAGTGAATTGCTTTGTTACAGTATAGTTTTATGATGATGAATACCTTCTTTAAAAAAAGCAATGTTGGTTTATAGAGTTTAAGATAAAAAAGTAACCAAGTGTTGGTATGGTGGCTCACACCTGTAATCCC... | GAGCTGGAGCCACTGATTGCAAAACAGCAAAAACATGGCTAAAGCCTTTAGGCAAGGTCACATTTAAATAGCCAGCGTTTCTAATCATTAATACAACTTCTACACTGTTGCTGTTTTTCACTTTTCCCAACCCATTGGTTGGTGTGATGAGTTAAATTCAAGGCCCAAAACCAACAAGTTCCAGGGTAAAAGTGAATTGCTTTGTTACAGTATAGTTTTATGATGATGAATACCTTCTTTAAAAAAAGCAATGTTGGTTTATAGAGTTTAAGATAAAAAAGTAACCAAGTGTTGGTATGGTGGCTCACACCTGTAATCCC... |
Task1_train_39965 | A mutation found on Chromosome 10 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CTACACTGTTGCTGTTTTTCACTTTTCCCAACCCATTGGTTGGTGTGATGAGTTAAATTCAAGGCCCAAAACCAACAAGTTCCAGGGTAAAAGTGAATTGCTTTGTTACAGTATAGTTTTATGATGATGAATACCTTCTTTAAAAAAAGCAATGTTGGTTTATAGAGTTTAAGATAAAAAAGTAACCAAGTGTTGGTATGGTGGCTCACACCTGTAATCCCAGCAGTTTTGGAGGCTGAGGCGGAAGAATTGCTTGAGGCCAAGAGTTCAAGACCAGCCTGGCCAATGCAGAAAGACCCTGTCTCTTAAAAAAAAATTAA... | CTACACTGTTGCTGTTTTTCACTTTTCCCAACCCATTGGTTGGTGTGATGAGTTAAATTCAAGGCCCAAAACCAACAAGTTCCAGGGTAAAAGTGAATTGCTTTGTTACAGTATAGTTTTATGATGATGAATACCTTCTTTAAAAAAAGCAATGTTGGTTTATAGAGTTTAAGATAAAAAAGTAACCAAGTGTTGGTATGGTGGCTCACACCTGTAATCCCAGCAGTTTTGGAGGCTGAGGCGGAAGAATTGCTTGAGGCCAAGAGTTCAAGACCAGCCTGGCCAATGCAGAAAGACCCTGTCTCTTAAAAAAAAATTAA... |
Task1_train_39966 | A mutation on Chromosome 10 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GATAAATTGGATTTATAAACTTTAAAAACTTCTTATCGAAATATACCATTAACAAAATGCATAGAAAAGCCCCTGAATGGGAAAATAAATGATAAGATGCATTTTCACATATGAATGCATGTAGCAAGTGCAATGAAAATAATATTCCATTTATAGTATGAACAATACATACAATAGTTGAATTTCAGGCATAAATATAAAGGGAAAAAATAACAGAAAAGTTGTACCTTGTACTTGATTGTAAAGACTGTAAGAAAGATAACACTTCCTAATTTAGTGAAGATATTTTAACATAAGACTAATTAATTTTTATCAGTATA... | GATAAATTGGATTTATAAACTTTAAAAACTTCTTATCGAAATATACCATTAACAAAATGCATAGAAAAGCCCCTGAATGGGAAAATAAATGATAAGATGCATTTTCACATATGAATGCATGTAGCAAGTGCAATGAAAATAATATTCCATTTATAGTATGAACAATACATACAATAGTTGAATTTCAGGCATAAATATAAAGGGAAAAAATAACAGAAAAGTTGTACCTTGTACTTGATTGTAAAGACTGTAAGAAAGATAACACTTCCTAATTTAGTGAAGATATTTTAACATAAGACTAATTAATTTTTATCAGTATA... |
Task1_train_39967 | This variant is found on Chromosome 10. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TACCACAATAAAGTATTTTTCATAAAGTAAGAGATTTAAAAACTAATCAAAGCTTTTTACCTAAAGCATGATGTGACTGCAAACAGAATGATGAGAATGTATGCCAGGTGAAACACAGGGATCACAGTCACAGAAGTTGCCTCAAATTCCAGTTGTCTGGAAAGCGATGTAAAGTGGACTACCTGCCACAAAAATATACTCAGATAAATAGCTTTTAATTACAATATTTGTGTGTGAGTTACAAAAACTATTGAAACACTTTATCTTAGTGATGAAACAATATGTATGTTAAAATTCAGCAAAAGATAAAAATACATGGA... | TACCACAATAAAGTATTTTTCATAAAGTAAGAGATTTAAAAACTAATCAAAGCTTTTTACCTAAAGCATGATGTGACTGCAAACAGAATGATGAGAATGTATGCCAGGTGAAACACAGGGATCACAGTCACAGAAGTTGCCTCAAATTCCAGTTGTCTGGAAAGCGATGTAAAGTGGACTACCTGCCACAAAAATATACTCAGATAAATAGCTTTTAATTACAATATTTGTGTGTGAGTTACAAAAACTATTGAAACACTTTATCTTAGTGATGAAACAATATGTATGTTAAAATTCAGCAAAAGATAAAAATACATGGA... |
Task1_train_39968 | This alteration on Chromosome 10 may affect genome function. Does it lead to a disease or is it benign? | Benign | GATCCATCTTGAATTAATTTTTGTATGAGATATAAGGTATGTATTCTTCAATATGCCTTATGCCTTGTTTTATTTTTGTTGTTTTCGTTGTTTTGCACATAGACAGTCTTATTTTAGTACCATGTGTTAAATGGAACATCATCTTTCCATTGAATTTAATTTGCATCTTTATAAAAAGCTACTTGACTACATATGTGTAACACTATTTCTAGGCTCTCTATTTTGTTACACTGTCCTATGTGTCTGTTTCCACAAATATCATCCTGTCTTGATTACTACAGCTTTATATTAAGTTCTAAAATCAAGCAATATGAGTCCTT... | GATCCATCTTGAATTAATTTTTGTATGAGATATAAGGTATGTATTCTTCAATATGCCTTATGCCTTGTTTTATTTTTGTTGTTTTCGTTGTTTTGCACATAGACAGTCTTATTTTAGTACCATGTGTTAAATGGAACATCATCTTTCCATTGAATTTAATTTGCATCTTTATAAAAAGCTACTTGACTACATATGTGTAACACTATTTCTAGGCTCTCTATTTTGTTACACTGTCCTATGTGTCTGTTTCCACAAATATCATCCTGTCTTGATTACTACAGCTTTATATTAAGTTCTAAAATCAAGCAATATGAGTCCTT... |
Task1_train_39969 | This mutation occurs on Chromosome 10. Does this change lead to a known medical condition, or is it benign? | Benign | AAAGCAATGCATTTGCAATCTAAGATAAAACACTCATGTTTTGGGCTGGGCATGGTGGCTCACACCTGTTATCCCAGCACTTTGGGAGGCCGAGGTGGGCAGATCACAAGGTCAGGAGTTTGAAATGAGCCTGACCAACAGTGTGAAACCTCATCTATACTAGAAACACAAAAATTAGCCAGGTGTGGTGGTGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCAGAGTTTGGAGTGAGCCCAGATGGCGCCACTGCACTCCAGCCTGGACAACAGAGTGAGATTCCAT... | AAAGCAATGCATTTGCAATCTAAGATAAAACACTCATGTTTTGGGCTGGGCATGGTGGCTCACACCTGTTATCCCAGCACTTTGGGAGGCCGAGGTGGGCAGATCACAAGGTCAGGAGTTTGAAATGAGCCTGACCAACAGTGTGAAACCTCATCTATACTAGAAACACAAAAATTAGCCAGGTGTGGTGGTGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCAGAGTTTGGAGTGAGCCCAGATGGCGCCACTGCACTCCAGCCTGGACAACAGAGTGAGATTCCAT... |
Task1_train_39970 | This variant is found on Chromosome 10. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | AACCAGTGATCTTGTTCTCGATGGGCCACCAGCCTTGCCAGAGGTACACCTCGTGGTGATTGTCAACAAGGAAAAGTGCTGTGAGGGCAGGGACAGGGCCAGACCATCAGGAGCTCCTTCACGGACACTTCTAGCTCACTCCTCCCCCAACCTAGTGGATGTTGTCCCTCTTGACTGCAGTGTCACAGGGGGAAACCCCCTTGGCCATCAAACCAGGGGCAAAGGGGCAAACAGAGAAACCCAGGATACCCCAGCCCTTTGACAGTTCAACGGGGAGAAGCCTGTAGGCAGAGAGAAGTGGTGTCAAGGAGTTGGTCTTT... | AACCAGTGATCTTGTTCTCGATGGGCCACCAGCCTTGCCAGAGGTACACCTCGTGGTGATTGTCAACAAGGAAAAGTGCTGTGAGGGCAGGGACAGGGCCAGACCATCAGGAGCTCCTTCACGGACACTTCTAGCTCACTCCTCCCCCAACCTAGTGGATGTTGTCCCTCTTGACTGCAGTGTCACAGGGGGAAACCCCCTTGGCCATCAAACCAGGGGCAAAGGGGCAAACAGAGAAACCCAGGATACCCCAGCCCTTTGACAGTTCAACGGGGAGAAGCCTGTAGGCAGAGAGAAGTGGTGTCAAGGAGTTGGTCTTT... |
Task1_train_39971 | This alteration occurs on Chromosome 10. Is it associated with a disease or is it a benign variant? | Benign | GGAGCTCCTTCACGGACACTTCTAGCTCACTCCTCCCCCAACCTAGTGGATGTTGTCCCTCTTGACTGCAGTGTCACAGGGGGAAACCCCCTTGGCCATCAAACCAGGGGCAAAGGGGCAAACAGAGAAACCCAGGATACCCCAGCCCTTTGACAGTTCAACGGGGAGAAGCCTGTAGGCAGAGAGAAGTGGTGTCAAGGAGTTGGTCTTTTTCATTCCTCGTCCTCCAGGTCCTCCTCCCTTTGCCCCAGCTCAAGGCCCTGGCCCTTCTGGATACTGGCAGGGCTGTGCTAAGAGTGGAAGGGATAATGCATGTGCCA... | GGAGCTCCTTCACGGACACTTCTAGCTCACTCCTCCCCCAACCTAGTGGATGTTGTCCCTCTTGACTGCAGTGTCACAGGGGGAAACCCCCTTGGCCATCAAACCAGGGGCAAAGGGGCAAACAGAGAAACCCAGGATACCCCAGCCCTTTGACAGTTCAACGGGGAGAAGCCTGTAGGCAGAGAGAAGTGGTGTCAAGGAGTTGGTCTTTTTCATTCCTCGTCCTCCAGGTCCTCCTCCCTTTGCCCCAGCTCAAGGCCCTGGCCCTTCTGGATACTGGCAGGGCTGTGCTAAGAGTGGAAGGGATAATGCATGTGCCA... |
Task1_train_39972 | Given this variant on Chromosome 10, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | AAGGAAAGGAGCAGTTCCAATTGCTTGCTCATAAGAAATTAAGTAGATGAGGAATGCTGCTCCCTTTGGGAGGCTGAAGTGGGAGGATGGTTTGAGCCCAGGAGTTTGAGACCAGCCTGGGCAACATAGTGAGACCTCATCTCTTAAAAAAAAAAAGAAAAAATTAGCTTGATAATGGTGGCATATGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCACGAGGATGGCTTGAGCCTGGGAGGTCAAGGCTGCAGTGAGCCGAGATTCTGCCATTGCACTCCAGCTTGGAAGACAGAGTGAAACCCTGTCTCAAAAAAA... | AAGGAAAGGAGCAGTTCCAATTGCTTGCTCATAAGAAATTAAGTAGATGAGGAATGCTGCTCCCTTTGGGAGGCTGAAGTGGGAGGATGGTTTGAGCCCAGGAGTTTGAGACCAGCCTGGGCAACATAGTGAGACCTCATCTCTTAAAAAAAAAAAGAAAAAATTAGCTTGATAATGGTGGCATATGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCACGAGGATGGCTTGAGCCTGGGAGGTCAAGGCTGCAGTGAGCCGAGATTCTGCCATTGCACTCCAGCTTGGAAGACAGAGTGAAACCCTGTCTCAAAAAAA... |
Task1_train_39973 | A genomic change on Chromosome 10 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GACAGGGTCTGAAATATTTACTTGGTCCCTACAAAGTGTCTTCCGTAGAGTAGGTGCTCAGGAAATGTTGTCAGCTGATGAATAGATGCATCTTGTATAAATCAGGAAAGAAATCCTGGTTCTGAGCCTGCAGTTTTCTGATCAGCAAACAGCTGCCTGTGCTTCCTGTGGCCCCGGGGGCAGGTGCACCTGCACAGCAAGGGGGCTGTAAAGAGGCAAAAATACTCTCTTCTGAGTTGAAATCACAAACCTGTGACCTGCATGCTCTCCTAAATGGGAAGGGGTGAGCAGCGCTGTGGAAAAGGCTCCTCCTTGGCAAT... | GACAGGGTCTGAAATATTTACTTGGTCCCTACAAAGTGTCTTCCGTAGAGTAGGTGCTCAGGAAATGTTGTCAGCTGATGAATAGATGCATCTTGTATAAATCAGGAAAGAAATCCTGGTTCTGAGCCTGCAGTTTTCTGATCAGCAAACAGCTGCCTGTGCTTCCTGTGGCCCCGGGGGCAGGTGCACCTGCACAGCAAGGGGGCTGTAAAGAGGCAAAAATACTCTCTTCTGAGTTGAAATCACAAACCTGTGACCTGCATGCTCTCCTAAATGGGAAGGGGTGAGCAGCGCTGTGGAAAAGGCTCCTCCTTGGCAAT... |
Task1_train_39974 | A sequence alteration has been identified on Chromosome 10. Is it disease-inducing or harmless? | Benign | AGATTTTTCTTCACCCAGTTTTCCTATCAACTATTCCATCATGTTTTTTTCCTACTGAATACTTTCTCCTTTTTTTGTACAAATTTATGTGGTGCATGAGAAATTTTGTTACACATATAAAATGCATAGTGATCAAGCCTCTATTTAGAATGTCCATCACCTCAGTACAATACGTTTTTATTTAGTCACCCTACTCTGCTATCAAACTCTGAATTTATTCCCACTATTGCATCTTTTGCTGCTTAATTCATCTGTGGTTAAGGGTTAACAAGGAAAACACATCCCCAAGGTAATTTACTTCCAGTTCTCTGTATCTGTCT... | AGATTTTTCTTCACCCAGTTTTCCTATCAACTATTCCATCATGTTTTTTTCCTACTGAATACTTTCTCCTTTTTTTGTACAAATTTATGTGGTGCATGAGAAATTTTGTTACACATATAAAATGCATAGTGATCAAGCCTCTATTTAGAATGTCCATCACCTCAGTACAATACGTTTTTATTTAGTCACCCTACTCTGCTATCAAACTCTGAATTTATTCCCACTATTGCATCTTTTGCTGCTTAATTCATCTGTGGTTAAGGGTTAACAAGGAAAACACATCCCCAAGGTAATTTACTTCCAGTTCTCTGTATCTGTCT... |
Task1_train_39975 | An alteration has been detected on Chromosome 10. Is it pathogenic, and if so, what disease is involved? | Benign | ATGATTACAGAAAAGCGGCGAAAAGATAAACTATGAAAGGGGTGTGAGAAACCCAGTAAGAGGGTCCTGAAGTGAGGAGTCCATGAAAGTGTCCCCATGACACCTGTTCAGTTTGTTTTTAAAACGAACATAAGACATAGGCATGGGCAAGGACTTCATGTCTAAAACACCAAAAGCAATGGCAACAAAAGCCAAAATTGACAAATGGGATCTAATTAAACTAAAGAGCTTCTGCACAGCAAAAGAAACTACCATCAGAGTGAACAGGCAACCCACAAAATGGGAGAAAATTTTCACAACCTACTCATCTGACAAAGGGC... | ATGATTACAGAAAAGCGGCGAAAAGATAAACTATGAAAGGGGTGTGAGAAACCCAGTAAGAGGGTCCTGAAGTGAGGAGTCCATGAAAGTGTCCCCATGACACCTGTTCAGTTTGTTTTTAAAACGAACATAAGACATAGGCATGGGCAAGGACTTCATGTCTAAAACACCAAAAGCAATGGCAACAAAAGCCAAAATTGACAAATGGGATCTAATTAAACTAAAGAGCTTCTGCACAGCAAAAGAAACTACCATCAGAGTGAACAGGCAACCCACAAAATGGGAGAAAATTTTCACAACCTACTCATCTGACAAAGGGC... |
Task1_train_39976 | This sequence change occurs on Chromosome 10. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GAAAGGGGTGGGAGGAGCAGAACCACCTGCTGGAGACTGGGTAGGAAGAGGGAAGGGCCCAGCTCAGGAGAGGGCATTCCTCTAACTCAACTCGTAAGGACCAAGTTTTTCTTTTCCCCTTACTGTAAAAGGCTTGGACTGGGCCGGGCTCAGTGGTTCACGCCTGTAATCCTGGCACTTTGGGAGGCCAAGGTGGGTGGATCACCTGAGGTCAGGAGTTCAAGACCAGCTTGGCCAATATGGCGAAACCCCATCTCTACTAAAAATACAAAAATAAACTGGGCCTGGTGACACACGCCTGTAGTCCCAGCTACTCAGGA... | GAAAGGGGTGGGAGGAGCAGAACCACCTGCTGGAGACTGGGTAGGAAGAGGGAAGGGCCCAGCTCAGGAGAGGGCATTCCTCTAACTCAACTCGTAAGGACCAAGTTTTTCTTTTCCCCTTACTGTAAAAGGCTTGGACTGGGCCGGGCTCAGTGGTTCACGCCTGTAATCCTGGCACTTTGGGAGGCCAAGGTGGGTGGATCACCTGAGGTCAGGAGTTCAAGACCAGCTTGGCCAATATGGCGAAACCCCATCTCTACTAAAAATACAAAAATAAACTGGGCCTGGTGACACACGCCTGTAGTCCCAGCTACTCAGGA... |
Task1_train_39977 | A sequence alteration has been identified on Chromosome 10. Is it disease-inducing or harmless? | Benign | GACTGGGCCGGGCTCAGTGGTTCACGCCTGTAATCCTGGCACTTTGGGAGGCCAAGGTGGGTGGATCACCTGAGGTCAGGAGTTCAAGACCAGCTTGGCCAATATGGCGAAACCCCATCTCTACTAAAAATACAAAAATAAACTGGGCCTGGTGACACACGCCTGTAGTCCCAGCTACTCAGGAGTCTGAGGTAGGAGAATCGCTTGCACCCAGGAGGCGGAGGTTGCAGTGAGCCGAGATCGTGCCACTGTACTCCAGCCTGGGGAACAGAGTGAGACTCTGTCTCAAAAAGAAAAAAATGGGAAGGGGAGGGGAGGGG... | GACTGGGCCGGGCTCAGTGGTTCACGCCTGTAATCCTGGCACTTTGGGAGGCCAAGGTGGGTGGATCACCTGAGGTCAGGAGTTCAAGACCAGCTTGGCCAATATGGCGAAACCCCATCTCTACTAAAAATACAAAAATAAACTGGGCCTGGTGACACACGCCTGTAGTCCCAGCTACTCAGGAGTCTGAGGTAGGAGAATCGCTTGCACCCAGGAGGCGGAGGTTGCAGTGAGCCGAGATCGTGCCACTGTACTCCAGCCTGGGGAACAGAGTGAGACTCTGTCTCAAAAAGAAAAAAATGGGAAGGGGAGGGGAGGGG... |
Task1_train_39978 | This is a variant located on Chromosome 10. Is this mutation a likely cause of disease or not? | Benign | GACTCCACCTCAAAAAATAACGTAACATAACATAACATAACAACATAACATTAACATAACAACATAACATTAACATAACATAACATAACGTAACATAACTGAACTGAACTGAACTAAGCATTCAACTCAAAAATAATAAAAGAGGCCGGGCTCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATCACATGAGATCAGGAGTTAGAGACCAGCCTGGCCAACGTGGTGAAACCCCAAATCTACTAAAAATACAAAAAATTAGCCAGGTGTGATGGCGCGTGCCTGTAATCCCTGCTACTTG... | GACTCCACCTCAAAAAATAACGTAACATAACATAACATAACAACATAACATTAACATAACAACATAACATTAACATAACATAACATAACGTAACATAACTGAACTGAACTGAACTAAGCATTCAACTCAAAAATAATAAAAGAGGCCGGGCTCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATCACATGAGATCAGGAGTTAGAGACCAGCCTGGCCAACGTGGTGAAACCCCAAATCTACTAAAAATACAAAAAATTAGCCAGGTGTGATGGCGCGTGCCTGTAATCCCTGCTACTTG... |
Task1_train_39979 | A mutation located on Chromosome 10 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GTCTGACTCAGTACTTTTCTCACTCATGCATACAAAGCAGCTAAAAATGACACAGCTTATTTACCATGCCCCTGACACTGCACTGAGCACTTTATGAGCTTGAACTCTGTTAATCCTCACGACCACCTCATGAGGTAGGTGCTGTTATTACTTCCATTTTACAGATGGGGAAAATTGAGGTCGAGAGAGGTTACGTTACTTGCTCAACGTCATGCAAGCAGTAAATGGGAGTGTGGGGGGAGGCAATGAGATTTGACTCCAAGCAGTCTGAGACCAGAGGAATGTTGGATTGCAGGATGCTAAACTGCTTTCCTCAGACA... | GTCTGACTCAGTACTTTTCTCACTCATGCATACAAAGCAGCTAAAAATGACACAGCTTATTTACCATGCCCCTGACACTGCACTGAGCACTTTATGAGCTTGAACTCTGTTAATCCTCACGACCACCTCATGAGGTAGGTGCTGTTATTACTTCCATTTTACAGATGGGGAAAATTGAGGTCGAGAGAGGTTACGTTACTTGCTCAACGTCATGCAAGCAGTAAATGGGAGTGTGGGGGGAGGCAATGAGATTTGACTCCAAGCAGTCTGAGACCAGAGGAATGTTGGATTGCAGGATGCTAAACTGCTTTCCTCAGACA... |
Task1_train_39980 | A change on Chromosome 10 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CCCACGCTCACTCACACATCCCTCACCACTCTGTGCCTGGCTCGCCCTTGGCAGGCATGGGATCTAGGCCGGTAGCATGAGCTGAGTGCAGCCTGCTAGGTTCCAAGTGGGTGGAACGAGCCTAATGGGCCAGAGCAAAACTCAGGCCAAGGCGCCACTGGCCACAGAGGTTTCCGGCTGGTGAAATGACACCCCAAGGATCCCATAGCAATAATACCAGGAAGCAGTGCTTGCAAAAAGGAATGACACCAGAAAGAGTGAACCCGAACTGATGGGAAAAACAGGGCAAATGAAGAGGGTGGGGTCTGGGCACCTTAAGG... | CCCACGCTCACTCACACATCCCTCACCACTCTGTGCCTGGCTCGCCCTTGGCAGGCATGGGATCTAGGCCGGTAGCATGAGCTGAGTGCAGCCTGCTAGGTTCCAAGTGGGTGGAACGAGCCTAATGGGCCAGAGCAAAACTCAGGCCAAGGCGCCACTGGCCACAGAGGTTTCCGGCTGGTGAAATGACACCCCAAGGATCCCATAGCAATAATACCAGGAAGCAGTGCTTGCAAAAAGGAATGACACCAGAAAGAGTGAACCCGAACTGATGGGAAAAACAGGGCAAATGAAGAGGGTGGGGTCTGGGCACCTTAAGG... |
Task1_train_39981 | This variant is located on Chromosome 10. Evaluate its biological effect and specify any disease association. | Benign | TGCCTAAGCCAACATCAGAAGGAAATGTGTACAACCCCTGATTAGTGCCAAAAAGACCAGATTGCACTAGGGAATGGAGAAAGAGTTAGAAAAATGAAACAGTATCTGTGAAAATCTTTACCTCTGGGAAATCTGAAGTATCCTAATAAATAACAGTGTATCATAATTTCATAAACTAGAGAAGCCATAATAAAATTTTGTCTTTTAAAAAGCTTTAAGGTTTCATTTATTTATTCAACAAATATTTACTGAGCAGCTATTATATGGCACTGTGGGAGGTAATGGGGTAACTCTGTTCCTGCTCTAATGAAGCTTTACTC... | TGCCTAAGCCAACATCAGAAGGAAATGTGTACAACCCCTGATTAGTGCCAAAAAGACCAGATTGCACTAGGGAATGGAGAAAGAGTTAGAAAAATGAAACAGTATCTGTGAAAATCTTTACCTCTGGGAAATCTGAAGTATCCTAATAAATAACAGTGTATCATAATTTCATAAACTAGAGAAGCCATAATAAAATTTTGTCTTTTAAAAAGCTTTAAGGTTTCATTTATTTATTCAACAAATATTTACTGAGCAGCTATTATATGGCACTGTGGGAGGTAATGGGGTAACTCTGTTCCTGCTCTAATGAAGCTTTACTC... |
Task1_train_39982 | An alteration has been detected on Chromosome 10. Is it pathogenic, and if so, what disease is involved? | Benign | CTAACTTTCCAGATCATTGAAGAGAATAACGAGAATAACTCTACTCTCCCTCCCACCCTCCCCTACGTTTTTTAAAAATCAAAATGTCCATGTTAACAAAGTGGGAAAAAAAAAAGTCCATGTTTTTTCACAAAATGGTCTGGTCCCTGGCACTGCTTTAAATAACTCCCCGCCTCCCCCTGCAAAAAAAGTCCAGGCTGGGGAAATCATCATTCATTCTAACTGTGTGGCAGGTTGTACATTCAGGCTTGAAGGTCTGTTTACCACAATAAAAAAAAAACCTGAGTGAGCATGATATTAAATGATGCAGGGGAGATAAA... | CTAACTTTCCAGATCATTGAAGAGAATAACGAGAATAACTCTACTCTCCCTCCCACCCTCCCCTACGTTTTTTAAAAATCAAAATGTCCATGTTAACAAAGTGGGAAAAAAAAAAGTCCATGTTTTTTCACAAAATGGTCTGGTCCCTGGCACTGCTTTAAATAACTCCCCGCCTCCCCCTGCAAAAAAAGTCCAGGCTGGGGAAATCATCATTCATTCTAACTGTGTGGCAGGTTGTACATTCAGGCTTGAAGGTCTGTTTACCACAATAAAAAAAAAACCTGAGTGAGCATGATATTAAATGATGCAGGGGAGATAAA... |
Task1_train_39983 | Assess the clinical impact of this variant found on Chromosome 10. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | ATTACCCAACTATTAAAAGGACTATGTAATCACAATCCTTATCCTGCATGACCTTGTGGTTATTATGTTTTGAAGCCCTGCCAGGAATGAATCAAAGAACCAAAACTAAAATCTGAAATTGAAGTCCAATAGAAACTGGGATGACTAGAGGTGGGAGGGAGGCGGGGTAAGGGTTGAAAAACTAGCTATCGGGTACTGTGCTCAGTACTTGGGTGACGGGATCATTGGTACCCCAAACCTCAGCATCACGCAGTATATCCAGGTAACAAACCTGCACATGTACCCACTAAATCTAAAACAAAAGTTAAAAAAAAAACCAC... | ATTACCCAACTATTAAAAGGACTATGTAATCACAATCCTTATCCTGCATGACCTTGTGGTTATTATGTTTTGAAGCCCTGCCAGGAATGAATCAAAGAACCAAAACTAAAATCTGAAATTGAAGTCCAATAGAAACTGGGATGACTAGAGGTGGGAGGGAGGCGGGGTAAGGGTTGAAAAACTAGCTATCGGGTACTGTGCTCAGTACTTGGGTGACGGGATCATTGGTACCCCAAACCTCAGCATCACGCAGTATATCCAGGTAACAAACCTGCACATGTACCCACTAAATCTAAAACAAAAGTTAAAAAAAAAACCAC... |
Task1_train_39984 | A variant has been detected on Chromosome 10. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TAGGGGTATATTAATAAAATTTAATATTCATTCTTATCAAAAATAGCGAGATATAAAGAAAAGTAAACTTTCTTAAGCTAATAAAGGCAATCTATTCATCTGTCATGGTTGCAGTGTGAACAAAAGAAAAGGAAAAGAAAAAAAGACAATGTATTTCAAGCTGATAAGCAATATACTTAAAGGTAAAATACTGCAGGCATTCCAATTAAACTCAGTTGAACCAAGATGTTGACTCTTACTACTCTTTTTAAAATTTTAGTTAAATAATACAACAAGAAATGAAAAAAAGCTATAAGCATTTCATAAATGAATAGACAAAA... | TAGGGGTATATTAATAAAATTTAATATTCATTCTTATCAAAAATAGCGAGATATAAAGAAAAGTAAACTTTCTTAAGCTAATAAAGGCAATCTATTCATCTGTCATGGTTGCAGTGTGAACAAAAGAAAAGGAAAAGAAAAAAAGACAATGTATTTCAAGCTGATAAGCAATATACTTAAAGGTAAAATACTGCAGGCATTCCAATTAAACTCAGTTGAACCAAGATGTTGACTCTTACTACTCTTTTTAAAATTTTAGTTAAATAATACAACAAGAAATGAAAAAAAGCTATAAGCATTTCATAAATGAATAGACAAAA... |
Task1_train_39985 | A mutation on Chromosome 10 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TGCTGTCAATATGCTTATATAAAAGCTGCTAAAATACATGCTCATAATTAGACTATTATACGGTAGTATTTAGACATGGAGTGATTATTAGAGAGTCTTAATCTAAAGCAGACAGTGAATGACACAAATTTAGTAAGATTTATAAACTATATTTTGGTTGTTTTTGGCAATTCACCAAATAATTGGGAGGGTGAAAACAACTTGCTTTATTATTATTTTCTTTGTGGCTATAGGCTGCCTTCTATAGTCATCATTGCTGTTCTCCTCCTCCTCCTCCTTCAACTCCTCCTCTTCCTTCTCCTCATTCTCCTCTTTCTCTT... | TGCTGTCAATATGCTTATATAAAAGCTGCTAAAATACATGCTCATAATTAGACTATTATACGGTAGTATTTAGACATGGAGTGATTATTAGAGAGTCTTAATCTAAAGCAGACAGTGAATGACACAAATTTAGTAAGATTTATAAACTATATTTTGGTTGTTTTTGGCAATTCACCAAATAATTGGGAGGGTGAAAACAACTTGCTTTATTATTATTTTCTTTGTGGCTATAGGCTGCCTTCTATAGTCATCATTGCTGTTCTCCTCCTCCTCCTCCTTCAACTCCTCCTCTTCCTTCTCCTCATTCTCCTCTTTCTCTT... |
Task1_train_39986 | A mutation has occurred on Chromosome 10. What is the medical relevance of this mutation? | Benign | GACTATGGCAGTGGCAAAAGCTGTGGGCCTATTGTGTTACCTCTGGAATCTCTGCCTCAGAGAAATGCAGAGCTGCAGCCAGCCCAAGTGATCAGGTTGGGGGGTGGGGTGAGGTGGGTTGCTGTGCTGGGGACCTAGGCCGATTGGCTTTGCTTGGCAAGGTGCCCCAGAGGTGAGGCCTCCAGTCTGTCCACATTTCAGTATCCTAGATGGGGCCCTTATCCTGGGGCGCATGGGAGATCCCTGCCTCCCTTCTTGGCAGAGCTATGGCAGCTGGTCCCAGGGTGCTCAGGAATCCAAAGCCCTTGGAGCTCCACATG... | GACTATGGCAGTGGCAAAAGCTGTGGGCCTATTGTGTTACCTCTGGAATCTCTGCCTCAGAGAAATGCAGAGCTGCAGCCAGCCCAAGTGATCAGGTTGGGGGGTGGGGTGAGGTGGGTTGCTGTGCTGGGGACCTAGGCCGATTGGCTTTGCTTGGCAAGGTGCCCCAGAGGTGAGGCCTCCAGTCTGTCCACATTTCAGTATCCTAGATGGGGCCCTTATCCTGGGGCGCATGGGAGATCCCTGCCTCCCTTCTTGGCAGAGCTATGGCAGCTGGTCCCAGGGTGCTCAGGAATCCAAAGCCCTTGGAGCTCCACATG... |
Task1_train_39987 | This is a variant located on Chromosome 10. Is this mutation a likely cause of disease or not? | Benign | GTCTGTGGTATGACTGAATGCATCACCCAGATAGCATAATACCCAAGAGGTCATTTTACCCCTTCTTCCTCCCCCTTTTAGTATTCCACAGTCTCTATGTCTGTGTTTACCCAGTGTTTATCTCCCACATATAAGGGAAGAGATGCAGTATTTGGTTTTCTGTTTCTGCATTAGCTCCCTCAGGATAATGGCCTCCAGCTGCATCCATGTTGCTGCAAAAGACATGATTTTGTTCTTTTTTATTGCTGTTTATTATTCCGTGGTATATATGTACCACATTTTCTATATCCAGTTCACCATTGATGAGCACCTACGTTGAT... | GTCTGTGGTATGACTGAATGCATCACCCAGATAGCATAATACCCAAGAGGTCATTTTACCCCTTCTTCCTCCCCCTTTTAGTATTCCACAGTCTCTATGTCTGTGTTTACCCAGTGTTTATCTCCCACATATAAGGGAAGAGATGCAGTATTTGGTTTTCTGTTTCTGCATTAGCTCCCTCAGGATAATGGCCTCCAGCTGCATCCATGTTGCTGCAAAAGACATGATTTTGTTCTTTTTTATTGCTGTTTATTATTCCGTGGTATATATGTACCACATTTTCTATATCCAGTTCACCATTGATGAGCACCTACGTTGAT... |
Task1_train_39988 | A variant on Chromosome 10 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | ATTCATCATGAATATCCTTTAATTAAGCTCTAGCATTTACTATCAGTGGAACATTAGCATATTATTGGTTTTAAAACTCATCCATTTGAAAAGTAATGCATAAAAATTCAGTGTTACAGTTACCTTAGAGTAGTCTCAATGTAGGCATTTCCAAAGCTATTCTACTTACTTTTGTTTCTGAAAAGTGATATTTAATTAGCAAAAGCAGAAAGGCAAAAGCACAAAGGCTAGCTGAAGACTGCGATGACAAGAGGAGTATAACACATAATTATTTCACTGGTTATCCATTCCTTCTATTTGATAAAAATGTCAGGCAAATT... | ATTCATCATGAATATCCTTTAATTAAGCTCTAGCATTTACTATCAGTGGAACATTAGCATATTATTGGTTTTAAAACTCATCCATTTGAAAAGTAATGCATAAAAATTCAGTGTTACAGTTACCTTAGAGTAGTCTCAATGTAGGCATTTCCAAAGCTATTCTACTTACTTTTGTTTCTGAAAAGTGATATTTAATTAGCAAAAGCAGAAAGGCAAAAGCACAAAGGCTAGCTGAAGACTGCGATGACAAGAGGAGTATAACACATAATTATTTCACTGGTTATCCATTCCTTCTATTTGATAAAAATGTCAGGCAAATT... |
Task1_train_39989 | Chromosome 10 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CAGAGCCAAGTTTCAACTTCTTCAACGGCCCAAAGATACACACCAGTAATAACTAAGAAGTCACCAAGTGCAAATAACATACATGCCACTCAGGCCTGCAATCCAGACTTTTTTACAAAACACATACACCCGAATTCTGGCCTGTATTTATTGCTCTTGCTGAAACAGTAGTATCTCCTCTGGCAAGCCAGATAGTTGTCTTTCTTCCCTAAGCTCTCCTTGCTCCAGATAATGTGCTACCTTTAAGTATTTAAAACTCTATTCATTTTGCTGATTTTTCTGCATTCATCAAGCTGTTTCTAAAGGGGAGTTCCGCATTG... | CAGAGCCAAGTTTCAACTTCTTCAACGGCCCAAAGATACACACCAGTAATAACTAAGAAGTCACCAAGTGCAAATAACATACATGCCACTCAGGCCTGCAATCCAGACTTTTTTACAAAACACATACACCCGAATTCTGGCCTGTATTTATTGCTCTTGCTGAAACAGTAGTATCTCCTCTGGCAAGCCAGATAGTTGTCTTTCTTCCCTAAGCTCTCCTTGCTCCAGATAATGTGCTACCTTTAAGTATTTAAAACTCTATTCATTTTGCTGATTTTTCTGCATTCATCAAGCTGTTTCTAAAGGGGAGTTCCGCATTG... |
Task1_train_39990 | The following genetic variant occurs on Chromosome 10. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TCAGAGCCCTAGTGTTGAAGAACATGTCACACCAGCACACGCCGCCGTCGCCAGCAGCAGGAAGTTGTTGATTTGCAGCATATTCACACTTTCTGATGCAGTCAGAGCTCACTGCTTCTCAGAACAGATCCACTCAGAAGGAACTCCAGTTTCTGATGTTTATTTTACTTTTTCTTCCCCCCAAACAAGGCACAAAAGGGGAAAATGAAAGGGACACAAGAAAAAAGGTAGCTGCACAGAGAGATAAATATAACACTGAAAATATTTTAGAAACCACAAGTTAAGGAAGGGAGAGATGGGAGAGAGATTCAGATATTTCT... | TCAGAGCCCTAGTGTTGAAGAACATGTCACACCAGCACACGCCGCCGTCGCCAGCAGCAGGAAGTTGTTGATTTGCAGCATATTCACACTTTCTGATGCAGTCAGAGCTCACTGCTTCTCAGAACAGATCCACTCAGAAGGAACTCCAGTTTCTGATGTTTATTTTACTTTTTCTTCCCCCCAAACAAGGCACAAAAGGGGAAAATGAAAGGGACACAAGAAAAAAGGTAGCTGCACAGAGAGATAAATATAACACTGAAAATATTTTAGAAACCACAAGTTAAGGAAGGGAGAGATGGGAGAGAGATTCAGATATTTCT... |
Task1_train_39991 | Here’s a variant located on Chromosome 10. What is the predicted biological effect — harmless or disease-causing? | Benign | TATCTTTGATTTATGCATTGAGCATGTACAATGCTATTAGTAAAAGTTTATTGTTAATAAAATAATTTTTGGGAAGATCAGCAATGTGAAATTTGCACAGATAAAAATAGTTTCTCACTTTCTATGTTTTAATTTTTATTTTTTGTGGATTAGTATATTCTGTGAACTTTTAGCATCTTCAGAAGAGAATCTTTTTATCTGTGCTTATTGATTTACATGTACATTTTATTAGACACATATTTTTATTATATATAGATTTATTACATATACGTCAATAACTACAGATTAATCATTTTAGTGTAGTTTTATTATTAGAAAAA... | TATCTTTGATTTATGCATTGAGCATGTACAATGCTATTAGTAAAAGTTTATTGTTAATAAAATAATTTTTGGGAAGATCAGCAATGTGAAATTTGCACAGATAAAAATAGTTTCTCACTTTCTATGTTTTAATTTTTATTTTTTGTGGATTAGTATATTCTGTGAACTTTTAGCATCTTCAGAAGAGAATCTTTTTATCTGTGCTTATTGATTTACATGTACATTTTATTAGACACATATTTTTATTATATATAGATTTATTACATATACGTCAATAACTACAGATTAATCATTTTAGTGTAGTTTTATTATTAGAAAAA... |
Task1_train_39992 | This alteration occurs on Chromosome 10. Is it associated with a disease or is it a benign variant? | Benign | TTGTGAAAATTCTCCACGGCTTCACATGCTAGTTCAGAAGATATTGATGCCTTGAGAATAAAGCATCTGGTTGTAACTCCAGCAGTTTTATATTTAAAGTATACCTAATATAATTGTCAACCACATTACTTTAGAAAACATAAACAAAAGATAGTTACACATATTTATTTTAAAAATGGTGACTGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACGTTGGGAGGCCGTGACTGGCAGATCACGAGGTTAGGAGATCGAGACCATCCTGACTAACAAGGCGAAACCCTGTCTCTACTAAAAATACAAAAAAATTAGTCG... | TTGTGAAAATTCTCCACGGCTTCACATGCTAGTTCAGAAGATATTGATGCCTTGAGAATAAAGCATCTGGTTGTAACTCCAGCAGTTTTATATTTAAAGTATACCTAATATAATTGTCAACCACATTACTTTAGAAAACATAAACAAAAGATAGTTACACATATTTATTTTAAAAATGGTGACTGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACGTTGGGAGGCCGTGACTGGCAGATCACGAGGTTAGGAGATCGAGACCATCCTGACTAACAAGGCGAAACCCTGTCTCTACTAAAAATACAAAAAAATTAGTCG... |
Task1_train_39993 | A variant found on Chromosome 10 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | AACTGTAATGTTTTCTATTTTGAACTTCTGTATTTCTTAAAGATTCAAGAAGGTGAATGTTGAAACTCCAATTTCTTTTTTTAGTTCTTCGAAGCTTGATTCAAATTCCACGGTTTATTTCGGGGATCCCATCTTTTACTGATATAACACTCGTGTTTTAACTTGAATTACCTCGTTTCCAGTGTTGTCACTTTGAGAATCCTAAGAAAATCAGTAACTCGGATTAGTGAACTCTGTGTGTTTATGTGTGTGTGTCTGCGTGTGTGCCTGTGTGTGCCTGTGTATGTGTGTGGTAACTTTACCTTGTGAAGATGAGGAAA... | AACTGTAATGTTTTCTATTTTGAACTTCTGTATTTCTTAAAGATTCAAGAAGGTGAATGTTGAAACTCCAATTTCTTTTTTTAGTTCTTCGAAGCTTGATTCAAATTCCACGGTTTATTTCGGGGATCCCATCTTTTACTGATATAACACTCGTGTTTTAACTTGAATTACCTCGTTTCCAGTGTTGTCACTTTGAGAATCCTAAGAAAATCAGTAACTCGGATTAGTGAACTCTGTGTGTTTATGTGTGTGTGTCTGCGTGTGTGCCTGTGTGTGCCTGTGTATGTGTGTGGTAACTTTACCTTGTGAAGATGAGGAAA... |
Task1_train_39994 | A mutation on Chromosome 10 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GTTTATTGCTGGTAATATTTTTGCTATGAAATGTACTTTGGTATTAATACAACCACCCTTCCTCAGCCTTCTTTTGTCAAGTGTTAGTGTGGTATATGTTGTTTCATCTTTAATCAATTTTTGTCTTTATATTTAAAGTTTATTTCTTATAGGCATTACACAGGTAGATCTTACTTTTATATCCATTCTGACAATCTGCTTTTGAGCAGAGGTTTTTAGACCACTTTAATTTATAATGTAATTATTGATATGATAAAAGTTTGCTGTCATCATGCTGTTTGATTTCTATTAGTTCCAGATCTTCTTTGCTTTGCTTTTGT... | GTTTATTGCTGGTAATATTTTTGCTATGAAATGTACTTTGGTATTAATACAACCACCCTTCCTCAGCCTTCTTTTGTCAAGTGTTAGTGTGGTATATGTTGTTTCATCTTTAATCAATTTTTGTCTTTATATTTAAAGTTTATTTCTTATAGGCATTACACAGGTAGATCTTACTTTTATATCCATTCTGACAATCTGCTTTTGAGCAGAGGTTTTTAGACCACTTTAATTTATAATGTAATTATTGATATGATAAAAGTTTGCTGTCATCATGCTGTTTGATTTCTATTAGTTCCAGATCTTCTTTGCTTTGCTTTTGT... |
Task1_train_39995 | A mutation is present on Chromosome 10. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TTTTGCTATGAAATGTACTTTGGTATTAATACAACCACCCTTCCTCAGCCTTCTTTTGTCAAGTGTTAGTGTGGTATATGTTGTTTCATCTTTAATCAATTTTTGTCTTTATATTTAAAGTTTATTTCTTATAGGCATTACACAGGTAGATCTTACTTTTATATCCATTCTGACAATCTGCTTTTGAGCAGAGGTTTTTAGACCACTTTAATTTATAATGTAATTATTGATATGATAAAAGTTTGCTGTCATCATGCTGTTTGATTTCTATTAGTTCCAGATCTTCTTTGCTTTGCTTTTGTTCTTTTTCTGCTTCCTTC... | TTTTGCTATGAAATGTACTTTGGTATTAATACAACCACCCTTCCTCAGCCTTCTTTTGTCAAGTGTTAGTGTGGTATATGTTGTTTCATCTTTAATCAATTTTTGTCTTTATATTTAAAGTTTATTTCTTATAGGCATTACACAGGTAGATCTTACTTTTATATCCATTCTGACAATCTGCTTTTGAGCAGAGGTTTTTAGACCACTTTAATTTATAATGTAATTATTGATATGATAAAAGTTTGCTGTCATCATGCTGTTTGATTTCTATTAGTTCCAGATCTTCTTTGCTTTGCTTTTGTTCTTTTTCTGCTTCCTTC... |
Task1_train_39996 | A sequence alteration has been identified on Chromosome 10. Is it disease-inducing or harmless? | Benign | ACCACCCTTCCTCAGCCTTCTTTTGTCAAGTGTTAGTGTGGTATATGTTGTTTCATCTTTAATCAATTTTTGTCTTTATATTTAAAGTTTATTTCTTATAGGCATTACACAGGTAGATCTTACTTTTATATCCATTCTGACAATCTGCTTTTGAGCAGAGGTTTTTAGACCACTTTAATTTATAATGTAATTATTGATATGATAAAAGTTTGCTGTCATCATGCTGTTTGATTTCTATTAGTTCCAGATCTTCTTTGCTTTGCTTTTGTTCTTTTTCTGCTTCCTTCAGACTAGTTTAGTAATTTTTATGATTTAGTTTT... | ACCACCCTTCCTCAGCCTTCTTTTGTCAAGTGTTAGTGTGGTATATGTTGTTTCATCTTTAATCAATTTTTGTCTTTATATTTAAAGTTTATTTCTTATAGGCATTACACAGGTAGATCTTACTTTTATATCCATTCTGACAATCTGCTTTTGAGCAGAGGTTTTTAGACCACTTTAATTTATAATGTAATTATTGATATGATAAAAGTTTGCTGTCATCATGCTGTTTGATTTCTATTAGTTCCAGATCTTCTTTGCTTTGCTTTTGTTCTTTTTCTGCTTCCTTCAGACTAGTTTAGTAATTTTTATGATTTAGTTTT... |
Task1_train_39997 | Consider a variant on Chromosome 10. Determine its clinical classification and disease relevance. | Benign | ATAAAAGCGTAACTCTACATTGCTTTTATTTTCAGCTCTAAGTAACAGAAAAACTTACTTTGTAAAGTGCTAGATCTTAGGCTCAAGGGCATGTGGTGTCTGCTACAACTACTCAACTCTGCTGGGGTAGTGCAAAGACAGCCACAGGTCAAACATAAATAGGTGTTTTTTGTTTGTATTCATGTTTTCAAAACTTTATTTATGGACACTGAAATTTGAATATCATATAATTTTCATGTGTCACAATATTCTTTGATTCTTTCAACCATTTAGAAATATAAAACCATTCTTAGCTTGCAGGATACAAAAATGGGTAGTGG... | ATAAAAGCGTAACTCTACATTGCTTTTATTTTCAGCTCTAAGTAACAGAAAAACTTACTTTGTAAAGTGCTAGATCTTAGGCTCAAGGGCATGTGGTGTCTGCTACAACTACTCAACTCTGCTGGGGTAGTGCAAAGACAGCCACAGGTCAAACATAAATAGGTGTTTTTTGTTTGTATTCATGTTTTCAAAACTTTATTTATGGACACTGAAATTTGAATATCATATAATTTTCATGTGTCACAATATTCTTTGATTCTTTCAACCATTTAGAAATATAAAACCATTCTTAGCTTGCAGGATACAAAAATGGGTAGTGG... |
Task1_train_39998 | This variant is located on Chromosome 10. Evaluate its biological effect and specify any disease association. | Benign | CCCTACTGTTACTTTGGAGTAACATAAGGCGAGTTTGTGGATAGTTATTGAACATTCAGGATGTCAACAGGCCCTTCTCCACAGTGTGAAGACTCTGAGGCATTATGGAGGCTGACTTGTGGCTGGAAATTTCTAATATCCAATTCATTCATAAGGTTTTTCTCCTATGTGTGTTCTCTGATGTACAATGAGATTTGACTTTTGAGAGAAGGTTTTCCTGCATGTGTTACATTCATAGGGCTTTTCCCCTGTATGTGATCTCTGATGTTTAGCAAGGTCTGATTTACGGTAAAAGATTTTTCCACATTCATTACACTGAC... | CCCTACTGTTACTTTGGAGTAACATAAGGCGAGTTTGTGGATAGTTATTGAACATTCAGGATGTCAACAGGCCCTTCTCCACAGTGTGAAGACTCTGAGGCATTATGGAGGCTGACTTGTGGCTGGAAATTTCTAATATCCAATTCATTCATAAGGTTTTTCTCCTATGTGTGTTCTCTGATGTACAATGAGATTTGACTTTTGAGAGAAGGTTTTCCTGCATGTGTTACATTCATAGGGCTTTTCCCCTGTATGTGATCTCTGATGTTTAGCAAGGTCTGATTTACGGTAAAAGATTTTTCCACATTCATTACACTGAC... |
Task1_train_39999 | Mutation context: Chromosome 10. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TCCAGTCTATCATTGTTGGACATTTGGGTTGGTTCCAAGTCTTTGCTATTGTGAATAGTGCGGCAATAAACATACGTTTGCATGTGTCTTTATAGCAGCATGATTTATAGTCCTTTGTCATTTCCTTCTTCTATACAGTCTTTATGTAGTCATCATTTTGTTATTATTGGTGTATTCTTTTTTTTTTGTGACAAGATCTTGCTTTGTCTCCCAGGCTGGAGTGCAGTGGTATGATCTTGGCTCACTTCAGCCTTGAACTCCCAGGCTCAAGTGGTCCTCCTGCTTCAGCCCCCCAAGTAGCTGGGACTACAGGAGTGCGC... | TCCAGTCTATCATTGTTGGACATTTGGGTTGGTTCCAAGTCTTTGCTATTGTGAATAGTGCGGCAATAAACATACGTTTGCATGTGTCTTTATAGCAGCATGATTTATAGTCCTTTGTCATTTCCTTCTTCTATACAGTCTTTATGTAGTCATCATTTTGTTATTATTGGTGTATTCTTTTTTTTTTGTGACAAGATCTTGCTTTGTCTCCCAGGCTGGAGTGCAGTGGTATGATCTTGGCTCACTTCAGCCTTGAACTCCCAGGCTCAAGTGGTCCTCCTGCTTCAGCCCCCCAAGTAGCTGGGACTACAGGAGTGCGC... |
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