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_41100 | A mutation has occurred on Chromosome 11. What is the medical relevance of this mutation? | Benign | TATATACAGAGGAGAAGAAACAATGAGTAATCTTTACAAGAGTAGATGGTAAAATAAAGCATTATAAAAGTGAGAATAGATAGAAAGCAAACTTTATGTAAATGAGCATGTGCTTTATAATAACTTGATACATCTACCATGACTTTGAGAAAAATGTGTTAGTGGTAATGAGATTGAGTATCTAGATCTAAGCAGTTTGGGAAAATCCAGTCTGCACAATGCAGTTTTCATGCATTCATCAATAAAAAACATTTGGAATTGTTAAAGTCATTGGCTCTCAGGTTAAAGTGATTACAGAAAATTATTCTTGCGATGTTGCA... | TATATACAGAGGAGAAGAAACAATGAGTAATCTTTACAAGAGTAGATGGTAAAATAAAGCATTATAAAAGTGAGAATAGATAGAAAGCAAACTTTATGTAAATGAGCATGTGCTTTATAATAACTTGATACATCTACCATGACTTTGAGAAAAATGTGTTAGTGGTAATGAGATTGAGTATCTAGATCTAAGCAGTTTGGGAAAATCCAGTCTGCACAATGCAGTTTTCATGCATTCATCAATAAAAAACATTTGGAATTGTTAAAGTCATTGGCTCTCAGGTTAAAGTGATTACAGAAAATTATTCTTGCGATGTTGCA... |
Task1_train_41101 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | ATTCATCAATAAAAAACATTTGGAATTGTTAAAGTCATTGGCTCTCAGGTTAAAGTGATTACAGAAAATTATTCTTGCGATGTTGCAAAGGACATTTCAAATTGAGGAGAGTGACTGGGAAATACAGTCATAATCTAGTTTTATAGTGTTAAGATTTTTATAAATAATTGTTTCAGGGAAATTGCTGAGTAATTGGTCCTTTTGGAAGATATCTTTCCTACAGGCACAAGCTTGTGGGAACTAGAGAAAGCTATTGTGTAATGGAAAAACATAAAGGAGAATGGGGAAAATATAGTTATGACTTAGACTAAAGCCACAAA... | ATTCATCAATAAAAAACATTTGGAATTGTTAAAGTCATTGGCTCTCAGGTTAAAGTGATTACAGAAAATTATTCTTGCGATGTTGCAAAGGACATTTCAAATTGAGGAGAGTGACTGGGAAATACAGTCATAATCTAGTTTTATAGTGTTAAGATTTTTATAAATAATTGTTTCAGGGAAATTGCTGAGTAATTGGTCCTTTTGGAAGATATCTTTCCTACAGGCACAAGCTTGTGGGAACTAGAGAAAGCTATTGTGTAATGGAAAAACATAAAGGAGAATGGGGAAAATATAGTTATGACTTAGACTAAAGCCACAAA... |
Task1_train_41102 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | AAAGTGAAATCACCCAGGCCCACTTGGTACTGGAAAGAATATGCTCATGATGAATGCTCTGTGTTGAGGGTTGCTTGTAGTGCATGTAAGGAAATGCATAGGACTGGAGCTTGGCACTCATTTCAGGGAAAGCTGAGAAGATGAAAAAAGAAATATACATGGATTTCTGCTGCATCGTCCTATTTTTATTCATGCTTTTTCACTCATAACAAGTCCATTTACTTTAGGTTTTATTATTTTCACTCCCCTGTCTTCTTAAAGTTTGTCTTATCATGAAAGAGAGATAACCGCTTGAGCTCAGAAGTTTGAGAACACCCTGG... | AAAGTGAAATCACCCAGGCCCACTTGGTACTGGAAAGAATATGCTCATGATGAATGCTCTGTGTTGAGGGTTGCTTGTAGTGCATGTAAGGAAATGCATAGGACTGGAGCTTGGCACTCATTTCAGGGAAAGCTGAGAAGATGAAAAAAGAAATATACATGGATTTCTGCTGCATCGTCCTATTTTTATTCATGCTTTTTCACTCATAACAAGTCCATTTACTTTAGGTTTTATTATTTTCACTCCCCTGTCTTCTTAAAGTTTGTCTTATCATGAAAGAGAGATAACCGCTTGAGCTCAGAAGTTTGAGAACACCCTGG... |
Task1_train_41103 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TTCCTCATGTTCCAAGCATACTTTTTGAATTTGTAAATACTAGAATATTTGTCTTTAACTGTTGCTTTTCAGGGCCACCTTAAGGTAGGATTACAGTCCTGCAGTTATTCACTTTTGTGTGGGCCAGCATATCATGGGGAATCATCTGAAAATGAGGCTCCTATGCTTTCTTCCACATTCAGGTTGCCATAGGGAATGCCCCATGAGACACAAATTCAGGCTGAGCAAGAAGAAGCAATACAGCAAGGTATGGGCCACGGACATCTGTAGCACTTGATTATGAAATTTACTTGTGTTTTCAGGAATAGGAGTGCTATTGG... | TTCCTCATGTTCCAAGCATACTTTTTGAATTTGTAAATACTAGAATATTTGTCTTTAACTGTTGCTTTTCAGGGCCACCTTAAGGTAGGATTACAGTCCTGCAGTTATTCACTTTTGTGTGGGCCAGCATATCATGGGGAATCATCTGAAAATGAGGCTCCTATGCTTTCTTCCACATTCAGGTTGCCATAGGGAATGCCCCATGAGACACAAATTCAGGCTGAGCAAGAAGAAGCAATACAGCAAGGTATGGGCCACGGACATCTGTAGCACTTGATTATGAAATTTACTTGTGTTTTCAGGAATAGGAGTGCTATTGG... |
Task1_train_41104 | A mutation found on Chromosome 11 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GTAGCACTTGATTATGAAATTTACTTGTGTTTTCAGGAATAGGAGTGCTATTGGCTGCTGCATATTTATACCCAGGATGCATGCAGGATAGATTATATCTCACTAAGAGGTGCACTGAATTTTGGAACAGATGAGGCAAGTATTTAAAGTTTTATTGTAATTTGAATTACATGCAAGCAAAGCTTGATAGTTAACTTCATGCTGCATTTTTTTTTCTGAGTAGTTTCAAGGAAATTCCAGTCACTAAATGTGACACAAGAGACTTGGTATTTGCCTTAATTGCCTGTTTTGATGCTTGTAAAGAGTAAGTTGTTAGTGAT... | GTAGCACTTGATTATGAAATTTACTTGTGTTTTCAGGAATAGGAGTGCTATTGGCTGCTGCATATTTATACCCAGGATGCATGCAGGATAGATTATATCTCACTAAGAGGTGCACTGAATTTTGGAACAGATGAGGCAAGTATTTAAAGTTTTATTGTAATTTGAATTACATGCAAGCAAAGCTTGATAGTTAACTTCATGCTGCATTTTTTTTTCTGAGTAGTTTCAAGGAAATTCCAGTCACTAAATGTGACACAAGAGACTTGGTATTTGCCTTAATTGCCTGTTTTGATGCTTGTAAAGAGTAAGTTGTTAGTGAT... |
Task1_train_41105 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | CAAGTATTTAAAGTTTTATTGTAATTTGAATTACATGCAAGCAAAGCTTGATAGTTAACTTCATGCTGCATTTTTTTTTCTGAGTAGTTTCAAGGAAATTCCAGTCACTAAATGTGACACAAGAGACTTGGTATTTGCCTTAATTGCCTGTTTTGATGCTTGTAAAGAGTAAGTTGTTAGTGATTCTCCAGAGTTTGAGTCCCTAGGGCTATGAAGTTAAATGAAAGAGTCTTGGTGCCTCAGGTATACACTGTCTGAAGAGACAGGAGGGTGGCAGCCTGTTTCTTTGTATGTAGCAGGTAAGTGTATTCAGGCTTTCT... | CAAGTATTTAAAGTTTTATTGTAATTTGAATTACATGCAAGCAAAGCTTGATAGTTAACTTCATGCTGCATTTTTTTTTCTGAGTAGTTTCAAGGAAATTCCAGTCACTAAATGTGACACAAGAGACTTGGTATTTGCCTTAATTGCCTGTTTTGATGCTTGTAAAGAGTAAGTTGTTAGTGATTCTCCAGAGTTTGAGTCCCTAGGGCTATGAAGTTAAATGAAAGAGTCTTGGTGCCTCAGGTATACACTGTCTGAAGAGACAGGAGGGTGGCAGCCTGTTTCTTTGTATGTAGCAGGTAAGTGTATTCAGGCTTTCT... |
Task1_train_41106 | With a mutation on Chromosome 11, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TAAAGAGTAAGTTGTTAGTGATTCTCCAGAGTTTGAGTCCCTAGGGCTATGAAGTTAAATGAAAGAGTCTTGGTGCCTCAGGTATACACTGTCTGAAGAGACAGGAGGGTGGCAGCCTGTTTCTTTGTATGTAGCAGGTAAGTGTATTCAGGCTTTCTATGAAACTGAAAATAGGGTCTTCCTGATACGGCAAATGGGGCCTTTGATTTTTTAAATGTTAAATCACTGTGTTATTCAATTCTGTGCCCAATAATATTAAAAAATGAGGTCAACACTCATGAAAATATTTAGCCTTATATCCATTGAAAATTATCTCATGA... | TAAAGAGTAAGTTGTTAGTGATTCTCCAGAGTTTGAGTCCCTAGGGCTATGAAGTTAAATGAAAGAGTCTTGGTGCCTCAGGTATACACTGTCTGAAGAGACAGGAGGGTGGCAGCCTGTTTCTTTGTATGTAGCAGGTAAGTGTATTCAGGCTTTCTATGAAACTGAAAATAGGGTCTTCCTGATACGGCAAATGGGGCCTTTGATTTTTTAAATGTTAAATCACTGTGTTATTCAATTCTGTGCCCAATAATATTAAAAAATGAGGTCAACACTCATGAAAATATTTAGCCTTATATCCATTGAAAATTATCTCATGA... |
Task1_train_41107 | Assess the clinical impact of this variant found on Chromosome 11. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GAGGGTGGTAGCAAGAGGCAATAGGAACAGGACTGTTCATGGAGGGACATGAACATGAGAACCACCTCTGAAGCAGAAAGAAGAGGAATTACTTTTTCTTTTTGAAAAGCATGTTGAAATGCCTCTCTATGGCAGGTTTCTCAACTAAGGCATCATTGAATTGTTGGTCCAGATAACGTTTTGTTGTATGTGCTGCAGGCAGGGACCTTCATGTACTTTGTAGAAGGCATTGTAGATTGTTCAACAACATCCCCACTACATGTCAATAGCACCCCCTTCCTCTTGTAACAACCAAAAATGTCCCCAGACATTGACAAATA... | GAGGGTGGTAGCAAGAGGCAATAGGAACAGGACTGTTCATGGAGGGACATGAACATGAGAACCACCTCTGAAGCAGAAAGAAGAGGAATTACTTTTTCTTTTTGAAAAGCATGTTGAAATGCCTCTCTATGGCAGGTTTCTCAACTAAGGCATCATTGAATTGTTGGTCCAGATAACGTTTTGTTGTATGTGCTGCAGGCAGGGACCTTCATGTACTTTGTAGAAGGCATTGTAGATTGTTCAACAACATCCCCACTACATGTCAATAGCACCCCCTTCCTCTTGTAACAACCAAAAATGTCCCCAGACATTGACAAATA... |
Task1_train_41108 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | AGAGCAATATAATGATTCTTTCCTATTATTGTTTTCTGTTTTCTCATGAAATGTATTCATGTTGCTGTACTATCTCAAGTTTTTAGTTCTTCTCCTTCATAGGTAATAGATGGACACAATGAATATATAATGTGTCTTGAAGGGAGAGAAAAGAAATAGACATGGAGACAGGGATAGACAGAGAGGACCTAGAAGAAAAGGGAAGTTTGCAAGTCAGACTCTTACACTAGTTATTTCTGGGTAAAAAGATTTTCCTCAATCCCATTCTCATGTGTTTTATCTTGATGCTGCTTTCTAATATATCTTTGTGGCAGTAACTG... | AGAGCAATATAATGATTCTTTCCTATTATTGTTTTCTGTTTTCTCATGAAATGTATTCATGTTGCTGTACTATCTCAAGTTTTTAGTTCTTCTCCTTCATAGGTAATAGATGGACACAATGAATATATAATGTGTCTTGAAGGGAGAGAAAAGAAATAGACATGGAGACAGGGATAGACAGAGAGGACCTAGAAGAAAAGGGAAGTTTGCAAGTCAGACTCTTACACTAGTTATTTCTGGGTAAAAAGATTTTCCTCAATCCCATTCTCATGTGTTTTATCTTGATGCTGCTTTCTAATATATCTTTGTGGCAGTAACTG... |
Task1_train_41109 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CCTAGTGCTGAGGGTGGCAGTAGGAGGCCCACGGGACTGTTCATGGAGGGACATGGACATGAGAACCACCTCTGAAGCAGAAAGAAGAGGAATTATTTTGTCTTTGTGCAAATCACTTTGAAATGTCTCTCTATGGCAGGTTTCTCAAATAAGGCACCATTAAAATGTTGGTCCAGATAATGTTTTGTTGTGTGTGCTGTGGGCAGGGACCTTCATGTGCTTTGTAGAGGTCATTGGAGAGTGTTTGGCAGCGTCCCCTCTACATGTCAATAGCACCCCCTTCCTCTTGTAACAACCAAAAATGTCTCCAGACATTGACA... | CCTAGTGCTGAGGGTGGCAGTAGGAGGCCCACGGGACTGTTCATGGAGGGACATGGACATGAGAACCACCTCTGAAGCAGAAAGAAGAGGAATTATTTTGTCTTTGTGCAAATCACTTTGAAATGTCTCTCTATGGCAGGTTTCTCAAATAAGGCACCATTAAAATGTTGGTCCAGATAATGTTTTGTTGTGTGTGCTGTGGGCAGGGACCTTCATGTGCTTTGTAGAGGTCATTGGAGAGTGTTTGGCAGCGTCCCCTCTACATGTCAATAGCACCCCCTTCCTCTTGTAACAACCAAAAATGTCTCCAGACATTGACA... |
Task1_train_41110 | The following genetic variant occurs on Chromosome 11. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | ATAAGGCACCATTAAAATGTTGGTCCAGATAATGTTTTGTTGTGTGTGCTGTGGGCAGGGACCTTCATGTGCTTTGTAGAGGTCATTGGAGAGTGTTTGGCAGCGTCCCCTCTACATGTCAATAGCACCCCCTTCCTCTTGTAACAACCAAAAATGTCTCCAGACATTGACAAATATTCCACTGGGATTCAAGTCACTCCTGACAAAGAAACACTGCTCTATGGGCAATTAACAGCTTGATTTTTTTCTTTATATTTGAAAACAGGAAGGGGTTTTTGAAAGTATGTACTAGTTTGATCTTGGGGAAGGACATGTAACAT... | ATAAGGCACCATTAAAATGTTGGTCCAGATAATGTTTTGTTGTGTGTGCTGTGGGCAGGGACCTTCATGTGCTTTGTAGAGGTCATTGGAGAGTGTTTGGCAGCGTCCCCTCTACATGTCAATAGCACCCCCTTCCTCTTGTAACAACCAAAAATGTCTCCAGACATTGACAAATATTCCACTGGGATTCAAGTCACTCCTGACAAAGAAACACTGCTCTATGGGCAATTAACAGCTTGATTTTTTTCTTTATATTTGAAAACAGGAAGGGGTTTTTGAAAGTATGTACTAGTTTGATCTTGGGGAAGGACATGTAACAT... |
Task1_train_41111 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | GGCAGCGTCCCCTCTACATGTCAATAGCACCCCCTTCCTCTTGTAACAACCAAAAATGTCTCCAGACATTGACAAATATTCCACTGGGATTCAAGTCACTCCTGACAAAGAAACACTGCTCTATGGGCAATTAACAGCTTGATTTTTTTCTTTATATTTGAAAACAGGAAGGGGTTTTTGAAAGTATGTACTAGTTTGATCTTGGGGAAGGACATGTAACATACTTCTCCTGGTCATTTTAAGAGAGAAAATCTTATCTTCAGAACATTTTAGTAATTTTCAATCTAGCATTTAGTTATATGCCTCCTGTATATCTTTGA... | GGCAGCGTCCCCTCTACATGTCAATAGCACCCCCTTCCTCTTGTAACAACCAAAAATGTCTCCAGACATTGACAAATATTCCACTGGGATTCAAGTCACTCCTGACAAAGAAACACTGCTCTATGGGCAATTAACAGCTTGATTTTTTTCTTTATATTTGAAAACAGGAAGGGGTTTTTGAAAGTATGTACTAGTTTGATCTTGGGGAAGGACATGTAACATACTTCTCCTGGTCATTTTAAGAGAGAAAATCTTATCTTCAGAACATTTTAGTAATTTTCAATCTAGCATTTAGTTATATGCCTCCTGTATATCTTTGA... |
Task1_train_41112 | Given this context: Chromosome 11 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AATTTTTTATGATAACCCCGCCCCTATGCCTAAATTTGAGAAACCCCACCATTCTCTCTGTATTAAAAACTCCTTTCTCATGAATGTCTTTAGAGTGGGGTGACACCTTAAGAATCTCATCTATATTATTGACAGGTAAGAGAAGGACAGAACGAGTGTCCTAGCTGATGATGTTAAGGGAAAGGAGAGGGGACCTAGAAAAAGAAAATGTCTTCGTCAATGTTTATAGGTTTTTATGATATTTATTCCTGAATGGGGACATTTTTCTAACTTCCATTCTCTATGTCTCATTTTGATAAATATTCAGAACACCTCTGCAT... | AATTTTTTATGATAACCCCGCCCCTATGCCTAAATTTGAGAAACCCCACCATTCTCTCTGTATTAAAAACTCCTTTCTCATGAATGTCTTTAGAGTGGGGTGACACCTTAAGAATCTCATCTATATTATTGACAGGTAAGAGAAGGACAGAACGAGTGTCCTAGCTGATGATGTTAAGGGAAAGGAGAGGGGACCTAGAAAAAGAAAATGTCTTCGTCAATGTTTATAGGTTTTTATGATATTTATTCCTGAATGGGGACATTTTTCTAACTTCCATTCTCTATGTCTCATTTTGATAAATATTCAGAACACCTCTGCAT... |
Task1_train_41113 | A variant was discovered on Chromosome 11. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TTACAGTGATAAAAATATCTAACTGTCTAAACTTACCGAATGATCTTATTTGTAACTCATATTATTGCTATTCATTTTATGACATGAGGTTATGACATGAGGTTATTGTTGTCATTTTGTGTGTTCCAAAAGTGTTTGATATATTTTTGAAAAATTTTAGATATCTAGTGTTTGCTGCAATAGATTTGTATGCATCATGGGTATATGGAATTCATATTAAAACATATATATGTGTACTGCATGTACTAATATTGGTACACTTAATTAAGTAAAAAAGGATAATTATTGAATACTGTAAATGTTGTGCTTTCATAACCTTA... | TTACAGTGATAAAAATATCTAACTGTCTAAACTTACCGAATGATCTTATTTGTAACTCATATTATTGCTATTCATTTTATGACATGAGGTTATGACATGAGGTTATTGTTGTCATTTTGTGTGTTCCAAAAGTGTTTGATATATTTTTGAAAAATTTTAGATATCTAGTGTTTGCTGCAATAGATTTGTATGCATCATGGGTATATGGAATTCATATTAAAACATATATATGTGTACTGCATGTACTAATATTGGTACACTTAATTAAGTAAAAAAGGATAATTATTGAATACTGTAAATGTTGTGCTTTCATAACCTTA... |
Task1_train_41114 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TATATGGAATTCATATTAAAACATATATATGTGTACTGCATGTACTAATATTGGTACACTTAATTAAGTAAAAAAGGATAATTATTGAATACTGTAAATGTTGTGCTTTCATAACCTTAAGCTTTTAGACATGATTTTAAGTTACTGAGGCAATGATGAGTTAAAAATGGTGATACTAAAGGAAATAAGAATGCTCTCCAAAATACCCTAGCTTAGAAATCAAAACACGATTGTTTAGCAGATAACTGTATAAGGAATGATTTGATACTTGATACTAGCTGTCATTTTAATTGAGGTTTACCTCAGATGAAACTGTGAAA... | TATATGGAATTCATATTAAAACATATATATGTGTACTGCATGTACTAATATTGGTACACTTAATTAAGTAAAAAAGGATAATTATTGAATACTGTAAATGTTGTGCTTTCATAACCTTAAGCTTTTAGACATGATTTTAAGTTACTGAGGCAATGATGAGTTAAAAATGGTGATACTAAAGGAAATAAGAATGCTCTCCAAAATACCCTAGCTTAGAAATCAAAACACGATTGTTTAGCAGATAACTGTATAAGGAATGATTTGATACTTGATACTAGCTGTCATTTTAATTGAGGTTTACCTCAGATGAAACTGTGAAA... |
Task1_train_41115 | With a mutation on Chromosome 11, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | AGCCTGTCACAGTGTCCCACAAATGAAACCTTGCAAAGCAGAGGTGTGTTTTGGGCTTTACTTACATTCTGCAATGTTTTCACAGAAGGACATTTTACAAGGACAGCAAAAAAACCTAAGACTTTCAATGTCTTTTAGATTACACAATCATAAGGGCTAATGAAAAGTGTCATTGAGTTTTGTATGATTTTGCAAACATGTGGCCTCAGCCATGTTTTCTCAACAAGTTTCTCATAGGGTTTTAGCATTATACATTGGAGCAGAGCTGAATGAAAGTAGGTGAACATGAAGAAAGCACCCACATGAATGCCTGTAACTTC... | AGCCTGTCACAGTGTCCCACAAATGAAACCTTGCAAAGCAGAGGTGTGTTTTGGGCTTTACTTACATTCTGCAATGTTTTCACAGAAGGACATTTTACAAGGACAGCAAAAAAACCTAAGACTTTCAATGTCTTTTAGATTACACAATCATAAGGGCTAATGAAAAGTGTCATTGAGTTTTGTATGATTTTGCAAACATGTGGCCTCAGCCATGTTTTCTCAACAAGTTTCTCATAGGGTTTTAGCATTATACATTGGAGCAGAGCTGAATGAAAGTAGGTGAACATGAAGAAAGCACCCACATGAATGCCTGTAACTTC... |
Task1_train_41116 | With a mutation on Chromosome 11, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TGAAGAAAGCACCCACATGAATGCCTGTAACTTCCTATGTAATTACTATGCATGTCTTTGTAGACTCATCACCTTGGTATCCATAACCATTTCATTTACTTAGAGCTTAGTGATGAGAAAACATGGGCACATAGAGGAGGCCTTTTGGAGACACACACTGGGGCCTTTTGGAGCGTGGAGGGTGGGAGACAGGAGAGGATTAGGAAAAAATAACTAATGGGTACTAAGCTTTTTACCTGGGTTTTGTATGATTTTGCAAATATATGGCCACATTCCTAGGTTAGGAAATAATCTGTACAACAAACCCCCATGACACAAGT... | TGAAGAAAGCACCCACATGAATGCCTGTAACTTCCTATGTAATTACTATGCATGTCTTTGTAGACTCATCACCTTGGTATCCATAACCATTTCATTTACTTAGAGCTTAGTGATGAGAAAACATGGGCACATAGAGGAGGCCTTTTGGAGACACACACTGGGGCCTTTTGGAGCGTGGAGGGTGGGAGACAGGAGAGGATTAGGAAAAAATAACTAATGGGTACTAAGCTTTTTACCTGGGTTTTGTATGATTTTGCAAATATATGGCCACATTCCTAGGTTAGGAAATAATCTGTACAACAAACCCCCATGACACAAGT... |
Task1_train_41117 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | ACACACACTGGGGCCTTTTGGAGCGTGGAGGGTGGGAGACAGGAGAGGATTAGGAAAAAATAACTAATGGGTACTAAGCTTTTTACCTGGGTTTTGTATGATTTTGCAAATATATGGCCACATTCCTAGGTTAGGAAATAATCTGTACAACAAACCCCCATGACACAAGTTTACCAATGTAACAAACTTTCACTTGTACCCCTAAATTTAAAAGTTTTTTAAAAACCTATAAAATATATATTCAAAGCACACATTATACCCTCACTTAACTAGACTTTGATATCTCACAAACATTCAAAAATGTTATACCGTGTGTTGGT... | ACACACACTGGGGCCTTTTGGAGCGTGGAGGGTGGGAGACAGGAGAGGATTAGGAAAAAATAACTAATGGGTACTAAGCTTTTTACCTGGGTTTTGTATGATTTTGCAAATATATGGCCACATTCCTAGGTTAGGAAATAATCTGTACAACAAACCCCCATGACACAAGTTTACCAATGTAACAAACTTTCACTTGTACCCCTAAATTTAAAAGTTTTTTAAAAACCTATAAAATATATATTCAAAGCACACATTATACCCTCACTTAACTAGACTTTGATATCTCACAAACATTCAAAAATGTTATACCGTGTGTTGGT... |
Task1_train_41118 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | CTTTTGGAGCGTGGAGGGTGGGAGACAGGAGAGGATTAGGAAAAAATAACTAATGGGTACTAAGCTTTTTACCTGGGTTTTGTATGATTTTGCAAATATATGGCCACATTCCTAGGTTAGGAAATAATCTGTACAACAAACCCCCATGACACAAGTTTACCAATGTAACAAACTTTCACTTGTACCCCTAAATTTAAAAGTTTTTTAAAAACCTATAAAATATATATTCAAAGCACACATTATACCCTCACTTAACTAGACTTTGATATCTCACAAACATTCAAAAATGTTATACCGTGTGTTGGTTTTTATTATTTATC... | CTTTTGGAGCGTGGAGGGTGGGAGACAGGAGAGGATTAGGAAAAAATAACTAATGGGTACTAAGCTTTTTACCTGGGTTTTGTATGATTTTGCAAATATATGGCCACATTCCTAGGTTAGGAAATAATCTGTACAACAAACCCCCATGACACAAGTTTACCAATGTAACAAACTTTCACTTGTACCCCTAAATTTAAAAGTTTTTTAAAAACCTATAAAATATATATTCAAAGCACACATTATACCCTCACTTAACTAGACTTTGATATCTCACAAACATTCAAAAATGTTATACCGTGTGTTGGTTTTTATTATTTATC... |
Task1_train_41119 | A mutation has occurred on Chromosome 11. What is the medical relevance of this mutation? | Benign | GTTGGGATGACAGGCATAACACATGCAGTCTTTGAGCAAAGAATGCTTGCAGTCTCACACTCGTGGTGTTTGTTCAATAAACAGACTGATAGATAGAATAGTACCTTTGAAAGAGTATTATATATGAACCACAAGAGGGACATTTAAATAGGGCTAGAAATAGGAAGAAGGGAAGAGAAGCAGAGTGGAAATGAATAGAGAATATCAACTCAACTAGACTTTACTGCATGTACCACTTTATCCTTCAATTCTTACATGTTGGACTTCCTTTCCTCTAAAAAGGCATTGCCCTGTCCACCTCAGGATGTCTAATTTTCAGC... | GTTGGGATGACAGGCATAACACATGCAGTCTTTGAGCAAAGAATGCTTGCAGTCTCACACTCGTGGTGTTTGTTCAATAAACAGACTGATAGATAGAATAGTACCTTTGAAAGAGTATTATATATGAACCACAAGAGGGACATTTAAATAGGGCTAGAAATAGGAAGAAGGGAAGAGAAGCAGAGTGGAAATGAATAGAGAATATCAACTCAACTAGACTTTACTGCATGTACCACTTTATCCTTCAATTCTTACATGTTGGACTTCCTTTCCTCTAAAAAGGCATTGCCCTGTCCACCTCAGGATGTCTAATTTTCAGC... |
Task1_train_41120 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CACAATAGATAAAATAATAATGTAAAGATTGAGACATTGTAAGAATTACCAAAATGTGACACAGAGACATGATATGAGAACATAATGTTGGAAAACTGGTGCCAGTAGACTTGCTTAACACAGTGTGGTCCTGAACTTTTAATTTGTGAAGAAAAAAACAATATCTGTGAAATGAAATAAAATGATACATGCTTGCATAACTGTAAACTTTCATATTTCCATTTCATAGCTTGTAAACAGTTATCATACATAATAATGATTTGCAGCACACAATATTAGTTACAGAAATACATTTTGTAATAATACACATACTTCTACAC... | CACAATAGATAAAATAATAATGTAAAGATTGAGACATTGTAAGAATTACCAAAATGTGACACAGAGACATGATATGAGAACATAATGTTGGAAAACTGGTGCCAGTAGACTTGCTTAACACAGTGTGGTCCTGAACTTTTAATTTGTGAAGAAAAAAACAATATCTGTGAAATGAAATAAAATGATACATGCTTGCATAACTGTAAACTTTCATATTTCCATTTCATAGCTTGTAAACAGTTATCATACATAATAATGATTTGCAGCACACAATATTAGTTACAGAAATACATTTTGTAATAATACACATACTTCTACAC... |
Task1_train_41121 | Assess the clinical impact of this variant found on Chromosome 11. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | AACATAATGTTGGAAAACTGGTGCCAGTAGACTTGCTTAACACAGTGTGGTCCTGAACTTTTAATTTGTGAAGAAAAAAACAATATCTGTGAAATGAAATAAAATGATACATGCTTGCATAACTGTAAACTTTCATATTTCCATTTCATAGCTTGTAAACAGTTATCATACATAATAATGATTTGCAGCACACAATATTAGTTACAGAAATACATTTTGTAATAATACACATACTTCTACACATCCTTCAATTAGAATTTTCAAACACACATTTCATGCATGGTTTTCTACCACAGTACTGGATTGATCTCCCTATGAGG... | AACATAATGTTGGAAAACTGGTGCCAGTAGACTTGCTTAACACAGTGTGGTCCTGAACTTTTAATTTGTGAAGAAAAAAACAATATCTGTGAAATGAAATAAAATGATACATGCTTGCATAACTGTAAACTTTCATATTTCCATTTCATAGCTTGTAAACAGTTATCATACATAATAATGATTTGCAGCACACAATATTAGTTACAGAAATACATTTTGTAATAATACACATACTTCTACACATCCTTCAATTAGAATTTTCAAACACACATTTCATGCATGGTTTTCTACCACAGTACTGGATTGATCTCCCTATGAGG... |
Task1_train_41122 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CATATTTCCATTTCATAGCTTGTAAACAGTTATCATACATAATAATGATTTGCAGCACACAATATTAGTTACAGAAATACATTTTGTAATAATACACATACTTCTACACATCCTTCAATTAGAATTTTCAAACACACATTTCATGCATGGTTTTCTACCACAGTACTGGATTGATCTCCCTATGAGGATACAATTACGATAGTGTAATAAATTAGAGATAGTATTCTTTTTCTGAGATTCCAGCAAAGAACGTTCCTCACATTCAGTAACACATTGGTGTATTTAAAAACAAGAGATAGTAAAACAAATATTTTGCATTG... | CATATTTCCATTTCATAGCTTGTAAACAGTTATCATACATAATAATGATTTGCAGCACACAATATTAGTTACAGAAATACATTTTGTAATAATACACATACTTCTACACATCCTTCAATTAGAATTTTCAAACACACATTTCATGCATGGTTTTCTACCACAGTACTGGATTGATCTCCCTATGAGGATACAATTACGATAGTGTAATAAATTAGAGATAGTATTCTTTTTCTGAGATTCCAGCAAAGAACGTTCCTCACATTCAGTAACACATTGGTGTATTTAAAAACAAGAGATAGTAAAACAAATATTTTGCATTG... |
Task1_train_41123 | This mutation occurs on Chromosome 11. Does this change lead to a known medical condition, or is it benign? | Benign | ATATGCATTCTTACATATTAGGGAAGTAGGAATTTCTTCAATTGAGCAGTTCTGAGACATTATCTTGAGAGGCTGTGCATTACTGTAAGGTAAAGATGTACTCCAGTGTCTTCATATACTCTGAGAGTGACTTCCCTTTACTCCCAAATTTGTTTTGCATCAATAAAACAAATTTCGTTATAAAAGTTTTTGAAAAAACACGTTTGTAATAACTATTGAAAATATATTACCTCTACAAGATCAAATTTCATTGATTTAGCTTGTAAAGTAAGAAGAATATATATATATATATATATATTTTTTTTTTTAAACAGAAGTCA... | ATATGCATTCTTACATATTAGGGAAGTAGGAATTTCTTCAATTGAGCAGTTCTGAGACATTATCTTGAGAGGCTGTGCATTACTGTAAGGTAAAGATGTACTCCAGTGTCTTCATATACTCTGAGAGTGACTTCCCTTTACTCCCAAATTTGTTTTGCATCAATAAAACAAATTTCGTTATAAAAGTTTTTGAAAAAACACGTTTGTAATAACTATTGAAAATATATTACCTCTACAAGATCAAATTTCATTGATTTAGCTTGTAAAGTAAGAAGAATATATATATATATATATATATTTTTTTTTTTAAACAGAAGTCA... |
Task1_train_41124 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TTCCCTTTACTCCCAAATTTGTTTTGCATCAATAAAACAAATTTCGTTATAAAAGTTTTTGAAAAAACACGTTTGTAATAACTATTGAAAATATATTACCTCTACAAGATCAAATTTCATTGATTTAGCTTGTAAAGTAAGAAGAATATATATATATATATATATATTTTTTTTTTTAAACAGAAGTCAATTTACTGCCCAAAATGCATGCAACAATTGAAGGGTAGGGTGGAATGGCATATCAGCTGAATCAGCTGAGGCAAGGTGGAATACAGAATTCATTCCAGATATTCAAATAAAAAACTTAAATAAGAGGACAA... | TTCCCTTTACTCCCAAATTTGTTTTGCATCAATAAAACAAATTTCGTTATAAAAGTTTTTGAAAAAACACGTTTGTAATAACTATTGAAAATATATTACCTCTACAAGATCAAATTTCATTGATTTAGCTTGTAAAGTAAGAAGAATATATATATATATATATATATTTTTTTTTTTAAACAGAAGTCAATTTACTGCCCAAAATGCATGCAACAATTGAAGGGTAGGGTGGAATGGCATATCAGCTGAATCAGCTGAGGCAAGGTGGAATACAGAATTCATTCCAGATATTCAAATAAAAAACTTAAATAAGAGGACAA... |
Task1_train_41125 | Located on Chromosome 11, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TATTTTTTTTTTTAAACAGAAGTCAATTTACTGCCCAAAATGCATGCAACAATTGAAGGGTAGGGTGGAATGGCATATCAGCTGAATCAGCTGAGGCAAGGTGGAATACAGAATTCATTCCAGATATTCAAATAAAAAACTTAAATAAGAGGACAATTTGTGTGATATATTATTTCCCCTGGTTTATCTTAACAACTTACTGCAAATTGGGTGGCTTAAGGCAATAGCAGATTAGTCACTCATCAGTTCTCTAGGCTCCTCCAAAATCACAACGTTGGCAGGAACTCACTTCCTTCAAAGGCTTTAAGGATGACTCATTC... | TATTTTTTTTTTTAAACAGAAGTCAATTTACTGCCCAAAATGCATGCAACAATTGAAGGGTAGGGTGGAATGGCATATCAGCTGAATCAGCTGAGGCAAGGTGGAATACAGAATTCATTCCAGATATTCAAATAAAAAACTTAAATAAGAGGACAATTTGTGTGATATATTATTTCCCCTGGTTTATCTTAACAACTTACTGCAAATTGGGTGGCTTAAGGCAATAGCAGATTAGTCACTCATCAGTTCTCTAGGCTCCTCCAAAATCACAACGTTGGCAGGAACTCACTTCCTTCAAAGGCTTTAAGGATGACTCATTC... |
Task1_train_41126 | The following genetic variant occurs on Chromosome 11. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CAAAATGCATGCAACAATTGAAGGGTAGGGTGGAATGGCATATCAGCTGAATCAGCTGAGGCAAGGTGGAATACAGAATTCATTCCAGATATTCAAATAAAAAACTTAAATAAGAGGACAATTTGTGTGATATATTATTTCCCCTGGTTTATCTTAACAACTTACTGCAAATTGGGTGGCTTAAGGCAATAGCAGATTAGTCACTCATCAGTTCTCTAGGCTCCTCCAAAATCACAACGTTGGCAGGAACTCACTTCCTTCAAAGGCTTTAAGGATGACTCATTCCTTGCCCCTTTTTGTTTTGGTGAATCTTGACCATC... | CAAAATGCATGCAACAATTGAAGGGTAGGGTGGAATGGCATATCAGCTGAATCAGCTGAGGCAAGGTGGAATACAGAATTCATTCCAGATATTCAAATAAAAAACTTAAATAAGAGGACAATTTGTGTGATATATTATTTCCCCTGGTTTATCTTAACAACTTACTGCAAATTGGGTGGCTTAAGGCAATAGCAGATTAGTCACTCATCAGTTCTCTAGGCTCCTCCAAAATCACAACGTTGGCAGGAACTCACTTCCTTCAAAGGCTTTAAGGATGACTCATTCCTTGCCCCTTTTTGTTTTGGTGAATCTTGACCATC... |
Task1_train_41127 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TGCAACAATTGAAGGGTAGGGTGGAATGGCATATCAGCTGAATCAGCTGAGGCAAGGTGGAATACAGAATTCATTCCAGATATTCAAATAAAAAACTTAAATAAGAGGACAATTTGTGTGATATATTATTTCCCCTGGTTTATCTTAACAACTTACTGCAAATTGGGTGGCTTAAGGCAATAGCAGATTAGTCACTCATCAGTTCTCTAGGCTCCTCCAAAATCACAACGTTGGCAGGAACTCACTTCCTTCAAAGGCTTTAAGGATGACTCATTCCTTGCCCCTTTTTGTTTTGGTGAATCTTGACCATCTTTGGTTTG... | TGCAACAATTGAAGGGTAGGGTGGAATGGCATATCAGCTGAATCAGCTGAGGCAAGGTGGAATACAGAATTCATTCCAGATATTCAAATAAAAAACTTAAATAAGAGGACAATTTGTGTGATATATTATTTCCCCTGGTTTATCTTAACAACTTACTGCAAATTGGGTGGCTTAAGGCAATAGCAGATTAGTCACTCATCAGTTCTCTAGGCTCCTCCAAAATCACAACGTTGGCAGGAACTCACTTCCTTCAAAGGCTTTAAGGATGACTCATTCCTTGCCCCTTTTTGTTTTGGTGAATCTTGACCATCTTTGGTTTG... |
Task1_train_41128 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | AAAACTGAACACCGCATATTCTCACTCATAGGTGGGAATTGAACAATGAAATCACATGGACACAGGAAGGGGAATATCACACTCTGGGGACTGTTGTGGGCTAGGGGGAGGGGGGAGGTGGGAGGGACAGCATTGGGAGATATACCTAATGCTAGACAACGAGTTAGTGGGTGCAGCGCACCAGCATGGCACATGTATACATATGTAACTAACCTGCACAATGTGCACATGTACCCTAAAACTTTAATTAAAAAAAAAAAAGTACACATTCAATGAATTAAAAACTAAGCAAAATCACCAAGTGATAAGAGCTCTTGATT... | AAAACTGAACACCGCATATTCTCACTCATAGGTGGGAATTGAACAATGAAATCACATGGACACAGGAAGGGGAATATCACACTCTGGGGACTGTTGTGGGCTAGGGGGAGGGGGGAGGTGGGAGGGACAGCATTGGGAGATATACCTAATGCTAGACAACGAGTTAGTGGGTGCAGCGCACCAGCATGGCACATGTATACATATGTAACTAACCTGCACAATGTGCACATGTACCCTAAAACTTTAATTAAAAAAAAAAAAGTACACATTCAATGAATTAAAAACTAAGCAAAATCACCAAGTGATAAGAGCTCTTGATT... |
Task1_train_41129 | A variant on Chromosome 11 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TTAAAAAAAAAAAAGTACACATTCAATGAATTAAAAACTAAGCAAAATCACCAAGTGATAAGAGCTCTTGATTTTAAAATATTTGTAGACTTTGTGAGTTTAGACATAAGAGACTTGAATTAGAGGGTAGGGAGCATAGCTCAAAACACGTCTAAAGCTCCGAATCTCAAAATAACTGGATTTCATCTCCCAAACATTGTTTCTAAGTTCTACATCAAAAGAAATATAAGCATTTACTTGTACAATATTTTAGTCCCATATGTAATTCCATTAAATCATACCAGTACAGGGGAGGCAGAGATAATACAGCGGTCAGCTGG... | TTAAAAAAAAAAAAGTACACATTCAATGAATTAAAAACTAAGCAAAATCACCAAGTGATAAGAGCTCTTGATTTTAAAATATTTGTAGACTTTGTGAGTTTAGACATAAGAGACTTGAATTAGAGGGTAGGGAGCATAGCTCAAAACACGTCTAAAGCTCCGAATCTCAAAATAACTGGATTTCATCTCCCAAACATTGTTTCTAAGTTCTACATCAAAAGAAATATAAGCATTTACTTGTACAATATTTTAGTCCCATATGTAATTCCATTAAATCATACCAGTACAGGGGAGGCAGAGATAATACAGCGGTCAGCTGG... |
Task1_train_41130 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | TATGTAATTCCATTAAATCATACCAGTACAGGGGAGGCAGAGATAATACAGCGGTCAGCTGGTATGGAAACCATAGGTGAGCTGCTTAGTGGACAGGGCTCCAGGGCCCGGTAACCACTGTGGTCCAGTAAGGTGAGAGAATAATCTGTAGGTGCATAGACAACACCAAATTATTCATGAACATCTATCTGGCCAAATTCACCCAAATGAACCATTGAGGGAAATAAGATGGTGGAGTTGGGCAACATTTTGTGACAGGCCATAGTGTCTGCTGTGCCCACATCCCAGATGATGTGAACATCGCCACTTCTATCAGGTGC... | TATGTAATTCCATTAAATCATACCAGTACAGGGGAGGCAGAGATAATACAGCGGTCAGCTGGTATGGAAACCATAGGTGAGCTGCTTAGTGGACAGGGCTCCAGGGCCCGGTAACCACTGTGGTCCAGTAAGGTGAGAGAATAATCTGTAGGTGCATAGACAACACCAAATTATTCATGAACATCTATCTGGCCAAATTCACCCAAATGAACCATTGAGGGAAATAAGATGGTGGAGTTGGGCAACATTTTGTGACAGGCCATAGTGTCTGCTGTGCCCACATCCCAGATGATGTGAACATCGCCACTTCTATCAGGTGC... |
Task1_train_41131 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TCTTGTTCTTGATTATTTTTTCATTTTTCCATACAATGTTTGTCCTTACAGAACCAGTTTAGAAGTCCAATCGCATATGCAGCCCTTCAAAACATACTAATGTTTCTGGAACCTCACACCAAACAGTGCTTACTTCAGAGATTAGAAAGTAAACTAAATCTTGAAAAAGAAAGCAACAATGATAGGGCATGAGTAAAAGATTTAGTATGCCAAACAATACATTTGTATATAGCACACACACACACACACACACGACTTATTTTTACAACAGAAAACAAATAATGCATCTATGATGTCAAAGACAAGATGAATATTGAGAA... | TCTTGTTCTTGATTATTTTTTCATTTTTCCATACAATGTTTGTCCTTACAGAACCAGTTTAGAAGTCCAATCGCATATGCAGCCCTTCAAAACATACTAATGTTTCTGGAACCTCACACCAAACAGTGCTTACTTCAGAGATTAGAAAGTAAACTAAATCTTGAAAAAGAAAGCAACAATGATAGGGCATGAGTAAAAGATTTAGTATGCCAAACAATACATTTGTATATAGCACACACACACACACACACACGACTTATTTTTACAACAGAAAACAAATAATGCATCTATGATGTCAAAGACAAGATGAATATTGAGAA... |
Task1_train_41132 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | ATTGAACAACATTTTTATTAGGTGAGTTTGAGGAAAAGTTGCAGGTATAAGAATACTGCTTAACACATGAGCTTTCAAAAGAAAATCTTTTGTCATGGGATTGCTTTAGAAATACACTAAGACAAAAACAATTCTAAATAGGAATCCAGACTTGAGCAAAAAATATAAATTTTTAATTCTCAAGAATGTGCACAAAAAACAAGTTAACAAGAAGTTAATTTGGCTCTTATTTCTAGCCTATCAATGAAAGGTAATATATACAGTACCTAATACTATCATCAAAACCATCAACATTTTTTCATCAACATCATAACATTTAG... | ATTGAACAACATTTTTATTAGGTGAGTTTGAGGAAAAGTTGCAGGTATAAGAATACTGCTTAACACATGAGCTTTCAAAAGAAAATCTTTTGTCATGGGATTGCTTTAGAAATACACTAAGACAAAAACAATTCTAAATAGGAATCCAGACTTGAGCAAAAAATATAAATTTTTAATTCTCAAGAATGTGCACAAAAAACAAGTTAACAAGAAGTTAATTTGGCTCTTATTTCTAGCCTATCAATGAAAGGTAATATATACAGTACCTAATACTATCATCAAAACCATCAACATTTTTTCATCAACATCATAACATTTAG... |
Task1_train_41133 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | TCCAGACTTGAGCAAAAAATATAAATTTTTAATTCTCAAGAATGTGCACAAAAAACAAGTTAACAAGAAGTTAATTTGGCTCTTATTTCTAGCCTATCAATGAAAGGTAATATATACAGTACCTAATACTATCATCAAAACCATCAACATTTTTTCATCAACATCATAACATTTAGGGTCCATTATACAGGAAATAGAGCTCTATACTAAATAACAACTTTTGTTATTTGATATTTAGCATTGTAGATGAGGCAAAAATAATGAACTTGAAAATAAGTGAAAGATTGCTGAAACATAGGATGTTTCCTCTGGGTGACTGA... | TCCAGACTTGAGCAAAAAATATAAATTTTTAATTCTCAAGAATGTGCACAAAAAACAAGTTAACAAGAAGTTAATTTGGCTCTTATTTCTAGCCTATCAATGAAAGGTAATATATACAGTACCTAATACTATCATCAAAACCATCAACATTTTTTCATCAACATCATAACATTTAGGGTCCATTATACAGGAAATAGAGCTCTATACTAAATAACAACTTTTGTTATTTGATATTTAGCATTGTAGATGAGGCAAAAATAATGAACTTGAAAATAAGTGAAAGATTGCTGAAACATAGGATGTTTCCTCTGGGTGACTGA... |
Task1_train_41134 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CAGGAAATAGAGCTCTATACTAAATAACAACTTTTGTTATTTGATATTTAGCATTGTAGATGAGGCAAAAATAATGAACTTGAAAATAAGTGAAAGATTGCTGAAACATAGGATGTTTCCTCTGGGTGACTGAATCCCAGGTACATCTAATTTTCTCATCTGCTTTTTCCTAAAATTTGTGTGTCTGTCTGTCTGTGAGTATAGTTTGCATGTTTCTCACATTGGGAAACTTGTTATTTTTTTAATGTCTGCATCTTACATTAGGCTTTAAGAAAAATGCCCTTCATGACAGGCAAGACAAAATGCCTTCATTGAATAAA... | CAGGAAATAGAGCTCTATACTAAATAACAACTTTTGTTATTTGATATTTAGCATTGTAGATGAGGCAAAAATAATGAACTTGAAAATAAGTGAAAGATTGCTGAAACATAGGATGTTTCCTCTGGGTGACTGAATCCCAGGTACATCTAATTTTCTCATCTGCTTTTTCCTAAAATTTGTGTGTCTGTCTGTCTGTGAGTATAGTTTGCATGTTTCTCACATTGGGAAACTTGTTATTTTTTTAATGTCTGCATCTTACATTAGGCTTTAAGAAAAATGCCCTTCATGACAGGCAAGACAAAATGCCTTCATTGAATAAA... |
Task1_train_41135 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GCAATAAATGAACAAAGGAAAATAATTAGGAAAAATTATAATTTTAAAATAACGACAGTTTTGAATTGTGTTCATTTACTTTTATGAATCTTGTTACCTTCTGATTCTTTTCTAATTAATTGTTTTACTTCTATAATAGTATCATACTGTTAAAATTTATTTTTTAATTTATTATTTTTCAGTATTTATTAAAAATAAATCAAAATAATTTATTATTTATGATTATGATTTTTAATTATTTTTAATAATTGTGAAATTAAAATTGCACAATTAAATATTTAAAAATTTAATTGTGAAAAATGTATTATTCCATCTTTGAT... | GCAATAAATGAACAAAGGAAAATAATTAGGAAAAATTATAATTTTAAAATAACGACAGTTTTGAATTGTGTTCATTTACTTTTATGAATCTTGTTACCTTCTGATTCTTTTCTAATTAATTGTTTTACTTCTATAATAGTATCATACTGTTAAAATTTATTTTTTAATTTATTATTTTTCAGTATTTATTAAAAATAAATCAAAATAATTTATTATTTATGATTATGATTTTTAATTATTTTTAATAATTGTGAAATTAAAATTGCACAATTAAATATTTAAAAATTTAATTGTGAAAAATGTATTATTCCATCTTTGAT... |
Task1_train_41136 | This genomic variant is located on Chromosome 11. Can you determine its pathogenicity and name any linked disease? | Benign | TTTTCAGTATTTATTAAAAATAAATCAAAATAATTTATTATTTATGATTATGATTTTTAATTATTTTTAATAATTGTGAAATTAAAATTGCACAATTAAATATTTAAAAATTTAATTGTGAAAAATGTATTATTCCATCTTTGATGGTGTCAGTCATAGAGTAACTATTTTTTCTGGAAATGCCTTCTCCACCACCCCTGTAAAATATTGAGAACATCACAAGAAAACACCAAGATAGGCTACATTTAGTCCTTGAACTTTTGTGCTTGGAAACATGCCAAACAATCTGCCTTGGCAAATGGTCCCCAGGGCCTACCAAA... | TTTTCAGTATTTATTAAAAATAAATCAAAATAATTTATTATTTATGATTATGATTTTTAATTATTTTTAATAATTGTGAAATTAAAATTGCACAATTAAATATTTAAAAATTTAATTGTGAAAAATGTATTATTCCATCTTTGATGGTGTCAGTCATAGAGTAACTATTTTTTCTGGAAATGCCTTCTCCACCACCCCTGTAAAATATTGAGAACATCACAAGAAAACACCAAGATAGGCTACATTTAGTCCTTGAACTTTTGTGCTTGGAAACATGCCAAACAATCTGCCTTGGCAAATGGTCCCCAGGGCCTACCAAA... |
Task1_train_41137 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | TGATTATGATTTTTAATTATTTTTAATAATTGTGAAATTAAAATTGCACAATTAAATATTTAAAAATTTAATTGTGAAAAATGTATTATTCCATCTTTGATGGTGTCAGTCATAGAGTAACTATTTTTTCTGGAAATGCCTTCTCCACCACCCCTGTAAAATATTGAGAACATCACAAGAAAACACCAAGATAGGCTACATTTAGTCCTTGAACTTTTGTGCTTGGAAACATGCCAAACAATCTGCCTTGGCAAATGGTCCCCAGGGCCTACCAAAAGGTGCATTGTCATCAGCCTCTGGTATATGAGATCCTCTGGAAT... | TGATTATGATTTTTAATTATTTTTAATAATTGTGAAATTAAAATTGCACAATTAAATATTTAAAAATTTAATTGTGAAAAATGTATTATTCCATCTTTGATGGTGTCAGTCATAGAGTAACTATTTTTTCTGGAAATGCCTTCTCCACCACCCCTGTAAAATATTGAGAACATCACAAGAAAACACCAAGATAGGCTACATTTAGTCCTTGAACTTTTGTGCTTGGAAACATGCCAAACAATCTGCCTTGGCAAATGGTCCCCAGGGCCTACCAAAAGGTGCATTGTCATCAGCCTCTGGTATATGAGATCCTCTGGAAT... |
Task1_train_41138 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | GTCAGTCATAGAGTAACTATTTTTTCTGGAAATGCCTTCTCCACCACCCCTGTAAAATATTGAGAACATCACAAGAAAACACCAAGATAGGCTACATTTAGTCCTTGAACTTTTGTGCTTGGAAACATGCCAAACAATCTGCCTTGGCAAATGGTCCCCAGGGCCTACCAAAAGGTGCATTGTCATCAGCCTCTGGTATATGAGATCCTCTGGAATTATCCAAGTGAGAGGGAAAGAATAATCTCCTTGTGGTCACAGTAGCTGCTGGTCTTCTTTGACAAATAACTTCTTGGTAATCTTTCCATTAGACCAGAACCTAA... | GTCAGTCATAGAGTAACTATTTTTTCTGGAAATGCCTTCTCCACCACCCCTGTAAAATATTGAGAACATCACAAGAAAACACCAAGATAGGCTACATTTAGTCCTTGAACTTTTGTGCTTGGAAACATGCCAAACAATCTGCCTTGGCAAATGGTCCCCAGGGCCTACCAAAAGGTGCATTGTCATCAGCCTCTGGTATATGAGATCCTCTGGAATTATCCAAGTGAGAGGGAAAGAATAATCTCCTTGTGGTCACAGTAGCTGCTGGTCTTCTTTGACAAATAACTTCTTGGTAATCTTTCCATTAGACCAGAACCTAA... |
Task1_train_41139 | The following genetic variant occurs on Chromosome 11. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GAGTAACTATTTTTTCTGGAAATGCCTTCTCCACCACCCCTGTAAAATATTGAGAACATCACAAGAAAACACCAAGATAGGCTACATTTAGTCCTTGAACTTTTGTGCTTGGAAACATGCCAAACAATCTGCCTTGGCAAATGGTCCCCAGGGCCTACCAAAAGGTGCATTGTCATCAGCCTCTGGTATATGAGATCCTCTGGAATTATCCAAGTGAGAGGGAAAGAATAATCTCCTTGTGGTCACAGTAGCTGCTGGTCTTCTTTGACAAATAACTTCTTGGTAATCTTTCCATTAGACCAGAACCTAAACAAAATTTC... | GAGTAACTATTTTTTCTGGAAATGCCTTCTCCACCACCCCTGTAAAATATTGAGAACATCACAAGAAAACACCAAGATAGGCTACATTTAGTCCTTGAACTTTTGTGCTTGGAAACATGCCAAACAATCTGCCTTGGCAAATGGTCCCCAGGGCCTACCAAAAGGTGCATTGTCATCAGCCTCTGGTATATGAGATCCTCTGGAATTATCCAAGTGAGAGGGAAAGAATAATCTCCTTGTGGTCACAGTAGCTGCTGGTCTTCTTTGACAAATAACTTCTTGGTAATCTTTCCATTAGACCAGAACCTAAACAAAATTTC... |
Task1_train_41140 | A mutation found on Chromosome 11 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AACCTAAACAAAATTTCTAGATTGGTTTATTTTAACTCAGAATAAAACATAATGAATACACCAAAATGTAAAAACAACTTATCTCAAGTAAAATAAATATTATAAAAAATTCATTTCCTCAGTTTTCATATTTTATTTATAACAAAAATTTGAGGTTGACAAATTTCCAGACAGATAATATAAGAAGAAACCTTTTTAATGAATGTTGACTCACACACAGTAAGTATTATTCTCAAAATTGGAAGATATTGTTCCAGATTTTATTTCAGATGGAATAAAATGCAGACTTTATCAGAATAATATATTAATACATACACATA... | AACCTAAACAAAATTTCTAGATTGGTTTATTTTAACTCAGAATAAAACATAATGAATACACCAAAATGTAAAAACAACTTATCTCAAGTAAAATAAATATTATAAAAAATTCATTTCCTCAGTTTTCATATTTTATTTATAACAAAAATTTGAGGTTGACAAATTTCCAGACAGATAATATAAGAAGAAACCTTTTTAATGAATGTTGACTCACACACAGTAAGTATTATTCTCAAAATTGGAAGATATTGTTCCAGATTTTATTTCAGATGGAATAAAATGCAGACTTTATCAGAATAATATATTAATACATACACATA... |
Task1_train_41141 | A mutation is present on Chromosome 11. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | AAGTACATGTACAAATAAGGCACAAAGGAAAATAATTAGGAAAAATTATAATGTTAACAAAATGTTAACGACAGTTTTGAATTGTTTTCATTTACTTTTTTTGAATTTTGTTATCTTCTGATTCTTTTCCAATTAACATGGTTTACATATACGATAGTATCGCACTTTTAAATATTAAGAAATTTAATTGTGAAAAATGTATTATTCCATCTTTGATGATGTCAGTCACAGAGTAACTATTTTTTCTGGAAATGCCTTCTCCACCACGCCTGTAAAATATTGAGAACATCACAAGAAAAGACCAATTCATAATTTCCTTC... | AAGTACATGTACAAATAAGGCACAAAGGAAAATAATTAGGAAAAATTATAATGTTAACAAAATGTTAACGACAGTTTTGAATTGTTTTCATTTACTTTTTTTGAATTTTGTTATCTTCTGATTCTTTTCCAATTAACATGGTTTACATATACGATAGTATCGCACTTTTAAATATTAAGAAATTTAATTGTGAAAAATGTATTATTCCATCTTTGATGATGTCAGTCACAGAGTAACTATTTTTTCTGGAAATGCCTTCTCCACCACGCCTGTAAAATATTGAGAACATCACAAGAAAAGACCAATTCATAATTTCCTTC... |
Task1_train_41142 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | AAATATTAAGAAATTTAATTGTGAAAAATGTATTATTCCATCTTTGATGATGTCAGTCACAGAGTAACTATTTTTTCTGGAAATGCCTTCTCCACCACGCCTGTAAAATATTGAGAACATCACAAGAAAAGACCAATTCATAATTTCCTTCATTTGTGTGGCTTCTAAGGTAAAAAGGAAAATCTTTGCACAAAGCCTAACATGGCTACATTTAGTCCTTGAACTTTTGTGCTTGGAAACATGCCAAACAATCTGCCTTGGCAAATGGCCCCCAGGGCCTACCAAAAGGTGCATTGTCATCAGCCTCTGGTATATGAGAT... | AAATATTAAGAAATTTAATTGTGAAAAATGTATTATTCCATCTTTGATGATGTCAGTCACAGAGTAACTATTTTTTCTGGAAATGCCTTCTCCACCACGCCTGTAAAATATTGAGAACATCACAAGAAAAGACCAATTCATAATTTCCTTCATTTGTGTGGCTTCTAAGGTAAAAAGGAAAATCTTTGCACAAAGCCTAACATGGCTACATTTAGTCCTTGAACTTTTGTGCTTGGAAACATGCCAAACAATCTGCCTTGGCAAATGGCCCCCAGGGCCTACCAAAAGGTGCATTGTCATCAGCCTCTGGTATATGAGAT... |
Task1_train_41143 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CATCACAAGAAAAGACCAATTCATAATTTCCTTCATTTGTGTGGCTTCTAAGGTAAAAAGGAAAATCTTTGCACAAAGCCTAACATGGCTACATTTAGTCCTTGAACTTTTGTGCTTGGAAACATGCCAAACAATCTGCCTTGGCAAATGGCCCCCAGGGCCTACCAAAAGGTGCATTGTCATCAGCCTCTGGTATATGAGATCCTCTGGAATTATCCGAGTGAGAGGGAAAGAATAATCTCCTTATGGTCACAGTGGCTGCCGGTCTTCTTTGACACATAACTTCTTGGTAATCTTTCCATTAGACCAGAACCTAAACA... | CATCACAAGAAAAGACCAATTCATAATTTCCTTCATTTGTGTGGCTTCTAAGGTAAAAAGGAAAATCTTTGCACAAAGCCTAACATGGCTACATTTAGTCCTTGAACTTTTGTGCTTGGAAACATGCCAAACAATCTGCCTTGGCAAATGGCCCCCAGGGCCTACCAAAAGGTGCATTGTCATCAGCCTCTGGTATATGAGATCCTCTGGAATTATCCGAGTGAGAGGGAAAGAATAATCTCCTTATGGTCACAGTGGCTGCCGGTCTTCTTTGACACATAACTTCTTGGTAATCTTTCCATTAGACCAGAACCTAAACA... |
Task1_train_41144 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CTAAGGTAAAAAGGAAAATCTTTGCACAAAGCCTAACATGGCTACATTTAGTCCTTGAACTTTTGTGCTTGGAAACATGCCAAACAATCTGCCTTGGCAAATGGCCCCCAGGGCCTACCAAAAGGTGCATTGTCATCAGCCTCTGGTATATGAGATCCTCTGGAATTATCCGAGTGAGAGGGAAAGAATAATCTCCTTATGGTCACAGTGGCTGCCGGTCTTCTTTGACACATAACTTCTTGGTAATCTTTCCATTAGACCAGAACCTAAACAAAATTTCTAGATTGGTTTATCATAACTCAGAATAAAACATAATGAAT... | CTAAGGTAAAAAGGAAAATCTTTGCACAAAGCCTAACATGGCTACATTTAGTCCTTGAACTTTTGTGCTTGGAAACATGCCAAACAATCTGCCTTGGCAAATGGCCCCCAGGGCCTACCAAAAGGTGCATTGTCATCAGCCTCTGGTATATGAGATCCTCTGGAATTATCCGAGTGAGAGGGAAAGAATAATCTCCTTATGGTCACAGTGGCTGCCGGTCTTCTTTGACACATAACTTCTTGGTAATCTTTCCATTAGACCAGAACCTAAACAAAATTTCTAGATTGGTTTATCATAACTCAGAATAAAACATAATGAAT... |
Task1_train_41145 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | CATGGCTACATTTAGTCCTTGAACTTTTGTGCTTGGAAACATGCCAAACAATCTGCCTTGGCAAATGGCCCCCAGGGCCTACCAAAAGGTGCATTGTCATCAGCCTCTGGTATATGAGATCCTCTGGAATTATCCGAGTGAGAGGGAAAGAATAATCTCCTTATGGTCACAGTGGCTGCCGGTCTTCTTTGACACATAACTTCTTGGTAATCTTTCCATTAGACCAGAACCTAAACAAAATTTCTAGATTGGTTTATCATAACTCAGAATAAAACATAATGAATGCACCAAAATGTAAAAACAACTTATCTCAAGGAAAA... | CATGGCTACATTTAGTCCTTGAACTTTTGTGCTTGGAAACATGCCAAACAATCTGCCTTGGCAAATGGCCCCCAGGGCCTACCAAAAGGTGCATTGTCATCAGCCTCTGGTATATGAGATCCTCTGGAATTATCCGAGTGAGAGGGAAAGAATAATCTCCTTATGGTCACAGTGGCTGCCGGTCTTCTTTGACACATAACTTCTTGGTAATCTTTCCATTAGACCAGAACCTAAACAAAATTTCTAGATTGGTTTATCATAACTCAGAATAAAACATAATGAATGCACCAAAATGTAAAAACAACTTATCTCAAGGAAAA... |
Task1_train_41146 | A variant on Chromosome 11 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TTGTCATCAGCCTCTGGTATATGAGATCCTCTGGAATTATCCGAGTGAGAGGGAAAGAATAATCTCCTTATGGTCACAGTGGCTGCCGGTCTTCTTTGACACATAACTTCTTGGTAATCTTTCCATTAGACCAGAACCTAAACAAAATTTCTAGATTGGTTTATCATAACTCAGAATAAAACATAATGAATGCACCAAAATGTAAAAACAACTTATCTCAAGGAAAACAAATATTATAAAAATTTTCATCTCCTTAAATAGTTTTCTTATTTTATTTATAACAAAAATTTGAAGTTGACAAATTTCCATACAGATAATAT... | TTGTCATCAGCCTCTGGTATATGAGATCCTCTGGAATTATCCGAGTGAGAGGGAAAGAATAATCTCCTTATGGTCACAGTGGCTGCCGGTCTTCTTTGACACATAACTTCTTGGTAATCTTTCCATTAGACCAGAACCTAAACAAAATTTCTAGATTGGTTTATCATAACTCAGAATAAAACATAATGAATGCACCAAAATGTAAAAACAACTTATCTCAAGGAAAACAAATATTATAAAAATTTTCATCTCCTTAAATAGTTTTCTTATTTTATTTATAACAAAAATTTGAAGTTGACAAATTTCCATACAGATAATAT... |
Task1_train_41147 | A genomic variant on Chromosome 11 is under review. What is the biological outcome — benign or pathogenic? | Benign | TTATCATAACTCAGAATAAAACATAATGAATGCACCAAAATGTAAAAACAACTTATCTCAAGGAAAACAAATATTATAAAAATTTTCATCTCCTTAAATAGTTTTCTTATTTTATTTATAACAAAAATTTGAAGTTGACAAATTTCCATACAGATAATATAAGAAGAAAGTTTTTTCATGAATGTTGACTTACACACAGTAAGTATTATTCTCAAAATTGGAAGATTTTGTTTCACATTTTACTTCAGATGAAATAAAATGGGGACTTTCGCAGAATAATATATTAATATATATTAATGTATATATTAATATATACACAT... | TTATCATAACTCAGAATAAAACATAATGAATGCACCAAAATGTAAAAACAACTTATCTCAAGGAAAACAAATATTATAAAAATTTTCATCTCCTTAAATAGTTTTCTTATTTTATTTATAACAAAAATTTGAAGTTGACAAATTTCCATACAGATAATATAAGAAGAAAGTTTTTTCATGAATGTTGACTTACACACAGTAAGTATTATTCTCAAAATTGGAAGATTTTGTTTCACATTTTACTTCAGATGAAATAAAATGGGGACTTTCGCAGAATAATATATTAATATATATTAATGTATATATTAATATATACACAT... |
Task1_train_41148 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | ATAACAAAAATTTGAAGTTGACAAATTTCCATACAGATAATATAAGAAGAAAGTTTTTTCATGAATGTTGACTTACACACAGTAAGTATTATTCTCAAAATTGGAAGATTTTGTTTCACATTTTACTTCAGATGAAATAAAATGGGGACTTTCGCAGAATAATATATTAATATATATTAATGTATATATTAATATATACACATATCATTTACTCTCTACCCTAAGTAATGTCAGGGTTTGTGAGACAAATGTAGAGTTGCCAGAATCAGAGTCTACAAGCAAAGTATACATTTTGAAAATATAATTTTTTGGAAGAAATT... | ATAACAAAAATTTGAAGTTGACAAATTTCCATACAGATAATATAAGAAGAAAGTTTTTTCATGAATGTTGACTTACACACAGTAAGTATTATTCTCAAAATTGGAAGATTTTGTTTCACATTTTACTTCAGATGAAATAAAATGGGGACTTTCGCAGAATAATATATTAATATATATTAATGTATATATTAATATATACACATATCATTTACTCTCTACCCTAAGTAATGTCAGGGTTTGTGAGACAAATGTAGAGTTGCCAGAATCAGAGTCTACAAGCAAAGTATACATTTTGAAAATATAATTTTTTGGAAGAAATT... |
Task1_train_41149 | A variant has been detected on Chromosome 11. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | AAAATTTGAAGTTGACAAATTTCCATACAGATAATATAAGAAGAAAGTTTTTTCATGAATGTTGACTTACACACAGTAAGTATTATTCTCAAAATTGGAAGATTTTGTTTCACATTTTACTTCAGATGAAATAAAATGGGGACTTTCGCAGAATAATATATTAATATATATTAATGTATATATTAATATATACACATATCATTTACTCTCTACCCTAAGTAATGTCAGGGTTTGTGAGACAAATGTAGAGTTGCCAGAATCAGAGTCTACAAGCAAAGTATACATTTTGAAAATATAATTTTTTGGAAGAAATTAGATTT... | AAAATTTGAAGTTGACAAATTTCCATACAGATAATATAAGAAGAAAGTTTTTTCATGAATGTTGACTTACACACAGTAAGTATTATTCTCAAAATTGGAAGATTTTGTTTCACATTTTACTTCAGATGAAATAAAATGGGGACTTTCGCAGAATAATATATTAATATATATTAATGTATATATTAATATATACACATATCATTTACTCTCTACCCTAAGTAATGTCAGGGTTTGTGAGACAAATGTAGAGTTGCCAGAATCAGAGTCTACAAGCAAAGTATACATTTTGAAAATATAATTTTTTGGAAGAAATTAGATTT... |
Task1_train_41150 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AAGGATAATTCTTCTTCATTAGGAATTCCCAGATTATTACATGCATACACATAAATAGTACTCCATTCATTTATTATCGCACTAGGTAAACCAATGATTTTTCAACTGATAAACTTTCATTGCATTATAATATTTAGGGTTGAAAATTTAATTAAAAACCCGACATCAATATATATAGATCTGGTAAAATTCATTATATTTCATTTGTCATATTTGGCTACAAACAATTTTATGGTCTTCTAGCATTTCTTCCTAAATCTAAAAATTGTCATTTGAGGACCTTGTTAATAGTTTATAAAAACTGAGTTTGGTGGAACAAA... | AAGGATAATTCTTCTTCATTAGGAATTCCCAGATTATTACATGCATACACATAAATAGTACTCCATTCATTTATTATCGCACTAGGTAAACCAATGATTTTTCAACTGATAAACTTTCATTGCATTATAATATTTAGGGTTGAAAATTTAATTAAAAACCCGACATCAATATATATAGATCTGGTAAAATTCATTATATTTCATTTGTCATATTTGGCTACAAACAATTTTATGGTCTTCTAGCATTTCTTCCTAAATCTAAAAATTGTCATTTGAGGACCTTGTTAATAGTTTATAAAAACTGAGTTTGGTGGAACAAA... |
Task1_train_41151 | A variant has been detected on Chromosome 11. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | CAGTAAAAATGGGAATGAATTTGGGACTGTGGAAAAGTGATTATGTTACCTCAAAAATCTCATCTTATGCAAACAAGATAGCTTTTTCCTGCCTTTTCATTCTTTCACTAAGTGGAAGAAAGATTGGCGTGAAAAGTAGACTGAATATCTCAACACCAAGGCAAATTAAAAGATATCCAATCACTACTTTTCCAGTTACTTGAGTCTAATTTTGTACTGTAGAGTTGTGTTTTGTTTCCTTTTTAATATTATAATTATTCATATCATTCATAATTATTCATATCATAATTATTCATACCATATCATAATTATTCATAATT... | CAGTAAAAATGGGAATGAATTTGGGACTGTGGAAAAGTGATTATGTTACCTCAAAAATCTCATCTTATGCAAACAAGATAGCTTTTTCCTGCCTTTTCATTCTTTCACTAAGTGGAAGAAAGATTGGCGTGAAAAGTAGACTGAATATCTCAACACCAAGGCAAATTAAAAGATATCCAATCACTACTTTTCCAGTTACTTGAGTCTAATTTTGTACTGTAGAGTTGTGTTTTGTTTCCTTTTTAATATTATAATTATTCATATCATTCATAATTATTCATATCATAATTATTCATACCATATCATAATTATTCATAATT... |
Task1_train_41152 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | ACTTGAGTCTAATTTTGTACTGTAGAGTTGTGTTTTGTTTCCTTTTTAATATTATAATTATTCATATCATTCATAATTATTCATATCATAATTATTCATACCATATCATAATTATTCATAATTATTCATGACTGAAGATTTAGTTTCTTTGGTCCTTTAGTCCTGAAGGAACTCTTTAACACAAGAACCTACTTACAAGTAAACTGAACACACACACAGAATGTCAACATAATCTTCCATATGTATCTTTCAGTCTAGTTCTTTATTTGTAGGATATATTCCTAAGTTTCAATGCCAGAATCCCCATTGGCACTTTTAAT... | ACTTGAGTCTAATTTTGTACTGTAGAGTTGTGTTTTGTTTCCTTTTTAATATTATAATTATTCATATCATTCATAATTATTCATATCATAATTATTCATACCATATCATAATTATTCATAATTATTCATGACTGAAGATTTAGTTTCTTTGGTCCTTTAGTCCTGAAGGAACTCTTTAACACAAGAACCTACTTACAAGTAAACTGAACACACACACAGAATGTCAACATAATCTTCCATATGTATCTTTCAGTCTAGTTCTTTATTTGTAGGATATATTCCTAAGTTTCAATGCCAGAATCCCCATTGGCACTTTTAAT... |
Task1_train_41153 | A variant on Chromosome 11 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | ATAATTATTCATATCATTCATAATTATTCATATCATAATTATTCATACCATATCATAATTATTCATAATTATTCATGACTGAAGATTTAGTTTCTTTGGTCCTTTAGTCCTGAAGGAACTCTTTAACACAAGAACCTACTTACAAGTAAACTGAACACACACACAGAATGTCAACATAATCTTCCATATGTATCTTTCAGTCTAGTTCTTTATTTGTAGGATATATTCCTAAGTTTCAATGCCAGAATCCCCATTGGCACTTTTAATATGAGTTTTTTGACTTTTGCCTTATGATTTTTATTTGATAAGTCTGGGATATA... | ATAATTATTCATATCATTCATAATTATTCATATCATAATTATTCATACCATATCATAATTATTCATAATTATTCATGACTGAAGATTTAGTTTCTTTGGTCCTTTAGTCCTGAAGGAACTCTTTAACACAAGAACCTACTTACAAGTAAACTGAACACACACACAGAATGTCAACATAATCTTCCATATGTATCTTTCAGTCTAGTTCTTTATTTGTAGGATATATTCCTAAGTTTCAATGCCAGAATCCCCATTGGCACTTTTAATATGAGTTTTTTGACTTTTGCCTTATGATTTTTATTTGATAAGTCTGGGATATA... |
Task1_train_41154 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TCCGATGTGCCTAATCACAAGAAACACTGTGCCTAGGGCATGACTACCCTCAGCATTCCTTCTGGGCATCAGACATAGTTTGTCATTTTGCCAACATTCTGCATTTACGAGAATAGTTTGCTGTTTACTCATATAGCCTCCAGTGGTATACTGAGTTGATCACAACCCTCACTCTTTCGGACTACAACATTCAACAATGGACTAATATCCAGAATCTACAAGTAAATCAAGCAAATCAGCAAGAAGTGAACAAATAATCCCATCAAAAAGTGGACAAAGGTCATGAATAGACAACTCCAAAAGAAGATATACTTATGACC... | TCCGATGTGCCTAATCACAAGAAACACTGTGCCTAGGGCATGACTACCCTCAGCATTCCTTCTGGGCATCAGACATAGTTTGTCATTTTGCCAACATTCTGCATTTACGAGAATAGTTTGCTGTTTACTCATATAGCCTCCAGTGGTATACTGAGTTGATCACAACCCTCACTCTTTCGGACTACAACATTCAACAATGGACTAATATCCAGAATCTACAAGTAAATCAAGCAAATCAGCAAGAAGTGAACAAATAATCCCATCAAAAAGTGGACAAAGGTCATGAATAGACAACTCCAAAAGAAGATATACTTATGACC... |
Task1_train_41155 | A mutation located on Chromosome 11 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | GTTCCAAGCTACTATGTTTGTAGTGATTTCTTACAGTAGCAATAGAAAACGAATACAAGAGACAACATCATTATTTTTACAAAATACACATGTGTAAGCCAAATTAAAAGGTAGAAAACACTGGAGTACTTCTTACTGACCTTAACTAATTTAGTAATATGCATAACATTGGTATAAATGCAAGTGTGAGTTTAGCCCTGTTACTCCAATGCTATTCATCTAGCCAGACCCAAAAGAATTGTTTCTAATGGGAAGTATAGTTCTCCAGTTACAATTATATCAGTTGATGAAGCCAAATACACATATCATAAAGTAGAAAA... | GTTCCAAGCTACTATGTTTGTAGTGATTTCTTACAGTAGCAATAGAAAACGAATACAAGAGACAACATCATTATTTTTACAAAATACACATGTGTAAGCCAAATTAAAAGGTAGAAAACACTGGAGTACTTCTTACTGACCTTAACTAATTTAGTAATATGCATAACATTGGTATAAATGCAAGTGTGAGTTTAGCCCTGTTACTCCAATGCTATTCATCTAGCCAGACCCAAAAGAATTGTTTCTAATGGGAAGTATAGTTCTCCAGTTACAATTATATCAGTTGATGAAGCCAAATACACATATCATAAAGTAGAAAA... |
Task1_train_41156 | With a mutation on Chromosome 11, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | AAGTAGAAAAAGATACACAAATAAACAGATAAGTAACATAAAGGCAAATGCCATAGAACTATTATTAATGTTGCCCTTGAGACCAGAAATGTCCCTCATATAGTGTGATTTTTCCTGCCTTCAGTGATTCTGCTCCTTTAAGGCTAAAGTTAGAAGTTGAAATATTGATTTGAGTCACACAGTCCCCGGATTGAGTATGCTTCTAACCTTCCTGAAAATATTATAACTGTACTTTATTTCCAGACACTACCTTTATTTCACATATAAGTGCCACTCTCCCTCACTCCATCATGCATTAGTAGCCTTTTACATGCAAAGAG... | AAGTAGAAAAAGATACACAAATAAACAGATAAGTAACATAAAGGCAAATGCCATAGAACTATTATTAATGTTGCCCTTGAGACCAGAAATGTCCCTCATATAGTGTGATTTTTCCTGCCTTCAGTGATTCTGCTCCTTTAAGGCTAAAGTTAGAAGTTGAAATATTGATTTGAGTCACACAGTCCCCGGATTGAGTATGCTTCTAACCTTCCTGAAAATATTATAACTGTACTTTATTTCCAGACACTACCTTTATTTCACATATAAGTGCCACTCTCCCTCACTCCATCATGCATTAGTAGCCTTTTACATGCAAAGAG... |
Task1_train_41157 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AGATATAATTTTACATGTTGTGTGCCTTTTTAAATTAAGTCCCAACTTTTATTTTGCCCATGTAACTGATGTGTATTCTTGATAACAAATTGTGTCTGATACATGAAAAGAAATTGTTTATTTTATGAAAGCTTTTAGTTTATAAAGTTTCAAATTTAGTGTACTCACCTTAGTTTGTATTTGCTAGCAAATTACCCAAAAGTGTTTGAGTGTTTTCTATCATTTCACATTTACATTTTCTAGATTATTATTAAAGTATATCCATTGTCCATAAGAGGTTTCACCTTTTATGAATTTTATCCATGTATATTTTATGCATT... | AGATATAATTTTACATGTTGTGTGCCTTTTTAAATTAAGTCCCAACTTTTATTTTGCCCATGTAACTGATGTGTATTCTTGATAACAAATTGTGTCTGATACATGAAAAGAAATTGTTTATTTTATGAAAGCTTTTAGTTTATAAAGTTTCAAATTTAGTGTACTCACCTTAGTTTGTATTTGCTAGCAAATTACCCAAAAGTGTTTGAGTGTTTTCTATCATTTCACATTTACATTTTCTAGATTATTATTAAAGTATATCCATTGTCCATAAGAGGTTTCACCTTTTATGAATTTTATCCATGTATATTTTATGCATT... |
Task1_train_41158 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | TTTCTATCATTTCACATTTACATTTTCTAGATTATTATTAAAGTATATCCATTGTCCATAAGAGGTTTCACCTTTTATGAATTTTATCCATGTATATTTTATGCATTGTGCTATAAATTTTATTATGAATTAACTCAACAAATGAATGATTGTATCTATTTTCCCAAGTCTGTAGTTTGGTTTTTTATTATATTTTTGGTACTTTTTGTCATGCAGACTTTACAATTTTTAAAGAATGAAAACAATCTTTCTGATTTTAAGTGGTGTTTAAAGATCTCTTCTATTCTAAAACATACACACAAGCACACACACGCCACACA... | TTTCTATCATTTCACATTTACATTTTCTAGATTATTATTAAAGTATATCCATTGTCCATAAGAGGTTTCACCTTTTATGAATTTTATCCATGTATATTTTATGCATTGTGCTATAAATTTTATTATGAATTAACTCAACAAATGAATGATTGTATCTATTTTCCCAAGTCTGTAGTTTGGTTTTTTATTATATTTTTGGTACTTTTTGTCATGCAGACTTTACAATTTTTAAAGAATGAAAACAATCTTTCTGATTTTAAGTGGTGTTTAAAGATCTCTTCTATTCTAAAACATACACACAAGCACACACACGCCACACA... |
Task1_train_41159 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AAAATAAATGCAGATGTATTATGTAGAAATATTCTGTGGGAGGATATGCTCTATATTTATACTTTTGAAGTGTGATTTAGATGTATTAATCATATTTTAGCAAAATATTCAAAATATTCATTATATGGAGATGAAAGAAAACAATACACATTTTTAAGTAAAGGTTACAAACATAAATGCCTGTGAATGTGCATTTTTGTGTATATCAATGACTATCAGCATGTATGTACATGTATACGTGAACATATGTATATGTATACATACATAAAGAAAATAGATGACACAGATTTTTCTACATGTAAGAACAGCATAGGTACAGG... | AAAATAAATGCAGATGTATTATGTAGAAATATTCTGTGGGAGGATATGCTCTATATTTATACTTTTGAAGTGTGATTTAGATGTATTAATCATATTTTAGCAAAATATTCAAAATATTCATTATATGGAGATGAAAGAAAACAATACACATTTTTAAGTAAAGGTTACAAACATAAATGCCTGTGAATGTGCATTTTTGTGTATATCAATGACTATCAGCATGTATGTACATGTATACGTGAACATATGTATATGTATACATACATAAAGAAAATAGATGACACAGATTTTTCTACATGTAAGAACAGCATAGGTACAGG... |
Task1_train_41160 | This sequence change occurs on Chromosome 11. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | AGTGTGATTTAGATGTATTAATCATATTTTAGCAAAATATTCAAAATATTCATTATATGGAGATGAAAGAAAACAATACACATTTTTAAGTAAAGGTTACAAACATAAATGCCTGTGAATGTGCATTTTTGTGTATATCAATGACTATCAGCATGTATGTACATGTATACGTGAACATATGTATATGTATACATACATAAAGAAAATAGATGACACAGATTTTTCTACATGTAAGAACAGCATAGGTACAGGGTCACTTATGATCTTTATTTTAAAACGTCCAAGAAAAAAAACAGGATTACACTAATAAATTAAACATT... | AGTGTGATTTAGATGTATTAATCATATTTTAGCAAAATATTCAAAATATTCATTATATGGAGATGAAAGAAAACAATACACATTTTTAAGTAAAGGTTACAAACATAAATGCCTGTGAATGTGCATTTTTGTGTATATCAATGACTATCAGCATGTATGTACATGTATACGTGAACATATGTATATGTATACATACATAAAGAAAATAGATGACACAGATTTTTCTACATGTAAGAACAGCATAGGTACAGGGTCACTTATGATCTTTATTTTAAAACGTCCAAGAAAAAAAACAGGATTACACTAATAAATTAAACATT... |
Task1_train_41161 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | TGTGTATATCAATGACTATCAGCATGTATGTACATGTATACGTGAACATATGTATATGTATACATACATAAAGAAAATAGATGACACAGATTTTTCTACATGTAAGAACAGCATAGGTACAGGGTCACTTATGATCTTTATTTTAAAACGTCCAAGAAAAAAAACAGGATTACACTAATAAATTAAACATTTTTATTATCGTCTAGGGAAAACTCTTGCTAACCAGGTTTTTCCTCTACTGTCATACCACAACAATCATCAACACAGAAGACTTCTGTGATCAAATGGGTAGGGATTTCTTCCTCCCACACCACGTGGTA... | TGTGTATATCAATGACTATCAGCATGTATGTACATGTATACGTGAACATATGTATATGTATACATACATAAAGAAAATAGATGACACAGATTTTTCTACATGTAAGAACAGCATAGGTACAGGGTCACTTATGATCTTTATTTTAAAACGTCCAAGAAAAAAAACAGGATTACACTAATAAATTAAACATTTTTATTATCGTCTAGGGAAAACTCTTGCTAACCAGGTTTTTCCTCTACTGTCATACCACAACAATCATCAACACAGAAGACTTCTGTGATCAAATGGGTAGGGATTTCTTCCTCCCACACCACGTGGTA... |
Task1_train_41162 | This sequence change occurs on Chromosome 11. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TAAAAAAATCTTCCACATGGATCTGTTAGGACATTTCTATAATAATATATATAAACACTTGGCCTTTTTTTTTCTTTCTAAAAGTGGTTTTAGTCTTATTTGTTCATTCTCTTCTTAATGTGTGGTCATCTTAACATGACAAAATTTTGGTATGTCTCACATCATGAATATAAATCATTTGTAAGTCACTGAATTCAGAATGGACCTGCATATGACAGAGTTGTCACCCCTTTTAAAACTTTCATAATCTATGACATGATAAAAGAAAAACAAAGTCACCTTGCTTAAATCTCCCCTCTAATTTTACCTCTAAATTTAGT... | TAAAAAAATCTTCCACATGGATCTGTTAGGACATTTCTATAATAATATATATAAACACTTGGCCTTTTTTTTTCTTTCTAAAAGTGGTTTTAGTCTTATTTGTTCATTCTCTTCTTAATGTGTGGTCATCTTAACATGACAAAATTTTGGTATGTCTCACATCATGAATATAAATCATTTGTAAGTCACTGAATTCAGAATGGACCTGCATATGACAGAGTTGTCACCCCTTTTAAAACTTTCATAATCTATGACATGATAAAAGAAAAACAAAGTCACCTTGCTTAAATCTCCCCTCTAATTTTACCTCTAAATTTAGT... |
Task1_train_41163 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TGTGGAATTCTAGAGCTCAAGGGCCTGGTATAAGAATTCAAATGCACAATATTCATAGCATACCTGAATTGAGTGAGCAGTTCATTTCCAAAGGTAAGAGAAAAGGAATCTGATCACTTGTAAAATATTAAGAAGCTCTCACCTTGAATTTAAGACTAAAACATATTTCTTACTATTTAAATATAAGAAAGAGGGTTCTGTTTAATGTGAAGCTGTATTACAAATTGAATCACATACTTTCCAAGGATCATAGGAGAGAATACGTGTGTTGTTTTAGCAACAGTTTATAAAAATAATTGTATTACTTGTTATTGGATGGT... | TGTGGAATTCTAGAGCTCAAGGGCCTGGTATAAGAATTCAAATGCACAATATTCATAGCATACCTGAATTGAGTGAGCAGTTCATTTCCAAAGGTAAGAGAAAAGGAATCTGATCACTTGTAAAATATTAAGAAGCTCTCACCTTGAATTTAAGACTAAAACATATTTCTTACTATTTAAATATAAGAAAGAGGGTTCTGTTTAATGTGAAGCTGTATTACAAATTGAATCACATACTTTCCAAGGATCATAGGAGAGAATACGTGTGTTGTTTTAGCAACAGTTTATAAAAATAATTGTATTACTTGTTATTGGATGGT... |
Task1_train_41164 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | ACAACTTTTCTGTATTAAGAAATGTAAAAATCAATGAATAAAGCATTTAATTCAAGGATTTATTTTTAAAACTAAAACTTGTACACATCAGGAGCAAGGCAATGATTTTTAAAAACACACAGAATTTTAACAAAGAAACAGTTTGACTCTTTACAGAAGTCAAGTTTTCAAATGTTTAACACACAAAAGAGATATCACTGCATGTAGATTTTTAATGTGGTGAGTTAATATTTCAAGTCCAAAACATTGTGAAATGAGTCTTGATTTTGCCTATGTACCAAGAAAAAATTTATATTAGCGTTGTCAATGACAAAGAGATT... | ACAACTTTTCTGTATTAAGAAATGTAAAAATCAATGAATAAAGCATTTAATTCAAGGATTTATTTTTAAAACTAAAACTTGTACACATCAGGAGCAAGGCAATGATTTTTAAAAACACACAGAATTTTAACAAAGAAACAGTTTGACTCTTTACAGAAGTCAAGTTTTCAAATGTTTAACACACAAAAGAGATATCACTGCATGTAGATTTTTAATGTGGTGAGTTAATATTTCAAGTCCAAAACATTGTGAAATGAGTCTTGATTTTGCCTATGTACCAAGAAAAAATTTATATTAGCGTTGTCAATGACAAAGAGATT... |
Task1_train_41165 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | TATAATATTTTTCAAATTTTCTCTAACAATATATGCTATTTTATTATAACTTAATTTTATCAAAATATTTTATTTCCTAAAGTCCAAATTGTGAACTACTGATATTATCTTTTTTTTTCCTTTTTAGTTGCTTGTGTGCCTGTAAATTAAATTAACCAAAAGTAATTTGTAAAACACAAGTGAATATCCTTCACAAAAGGCATTGTGCTGGAATGCAAGTCTTCTAATGAGAATAGGCAGCATTGATTATTGTCACCTTAAATACTTTACAGCTACTCTCTGATCAAATTTGGAGTTATTATTTATCTTGTGCACTTAAG... | TATAATATTTTTCAAATTTTCTCTAACAATATATGCTATTTTATTATAACTTAATTTTATCAAAATATTTTATTTCCTAAAGTCCAAATTGTGAACTACTGATATTATCTTTTTTTTTCCTTTTTAGTTGCTTGTGTGCCTGTAAATTAAATTAACCAAAAGTAATTTGTAAAACACAAGTGAATATCCTTCACAAAAGGCATTGTGCTGGAATGCAAGTCTTCTAATGAGAATAGGCAGCATTGATTATTGTCACCTTAAATACTTTACAGCTACTCTCTGATCAAATTTGGAGTTATTATTTATCTTGTGCACTTAAG... |
Task1_train_41166 | This is a variant located on Chromosome 11. Is this mutation a likely cause of disease or not? | Benign | AAAATATTTTATTTCCTAAAGTCCAAATTGTGAACTACTGATATTATCTTTTTTTTTCCTTTTTAGTTGCTTGTGTGCCTGTAAATTAAATTAACCAAAAGTAATTTGTAAAACACAAGTGAATATCCTTCACAAAAGGCATTGTGCTGGAATGCAAGTCTTCTAATGAGAATAGGCAGCATTGATTATTGTCACCTTAAATACTTTACAGCTACTCTCTGATCAAATTTGGAGTTATTATTTATCTTGTGCACTTAAGGAAAGAGAGTTTTAAATTTTAGGTAACATATTCTGGGTTGTATAGCTGAAAATGTAGCATA... | AAAATATTTTATTTCCTAAAGTCCAAATTGTGAACTACTGATATTATCTTTTTTTTTCCTTTTTAGTTGCTTGTGTGCCTGTAAATTAAATTAACCAAAAGTAATTTGTAAAACACAAGTGAATATCCTTCACAAAAGGCATTGTGCTGGAATGCAAGTCTTCTAATGAGAATAGGCAGCATTGATTATTGTCACCTTAAATACTTTACAGCTACTCTCTGATCAAATTTGGAGTTATTATTTATCTTGTGCACTTAAGGAAAGAGAGTTTTAAATTTTAGGTAACATATTCTGGGTTGTATAGCTGAAAATGTAGCATA... |
Task1_train_41167 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AGCTAAAATAATTCCAAGTAGGGTAAATTGAAAGGAAATTATGCTAAAATGCATTATAGTCAAATTTCTGAAAACCAATAACAAAGAAAAATTCTTAAAAACAGCCAGAGATAAATGATACATCATAAACAAATGAAGAAATTATTTGCCACTGATTTCTTGACATAAACAATACAATTAATAAAATATTATCTTCTCTCAGCTTAATATAGTTTATAAGAAATTGTTTTATGTCAGTTTATAATCATATATTCAACAAAATATATGTGGTCAATGGATGTATTATCAAATATTATATAACTTTTTTCAAGAAAGTCATT... | AGCTAAAATAATTCCAAGTAGGGTAAATTGAAAGGAAATTATGCTAAAATGCATTATAGTCAAATTTCTGAAAACCAATAACAAAGAAAAATTCTTAAAAACAGCCAGAGATAAATGATACATCATAAACAAATGAAGAAATTATTTGCCACTGATTTCTTGACATAAACAATACAATTAATAAAATATTATCTTCTCTCAGCTTAATATAGTTTATAAGAAATTGTTTTATGTCAGTTTATAATCATATATTCAACAAAATATATGTGGTCAATGGATGTATTATCAAATATTATATAACTTTTTTCAAGAAAGTCATT... |
Task1_train_41168 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | ATACAATTAATAAAATATTATCTTCTCTCAGCTTAATATAGTTTATAAGAAATTGTTTTATGTCAGTTTATAATCATATATTCAACAAAATATATGTGGTCAATGGATGTATTATCAAATATTATATAACTTTTTTCAAGAAAGTCATTATTTCACTTACTTGTGACTTGTTGGGGATTATATATGTAATATTTGCATGCAATGCTGAAAATGGCATTTGTGATTTCCAGTCTTTAGTGATATTGCATAATTTATTTTTTCAGTTAGACAAAGGCATAAGTATTTACGACTTTTTCTTAATGGAACATTCGGAGAATAAT... | ATACAATTAATAAAATATTATCTTCTCTCAGCTTAATATAGTTTATAAGAAATTGTTTTATGTCAGTTTATAATCATATATTCAACAAAATATATGTGGTCAATGGATGTATTATCAAATATTATATAACTTTTTTCAAGAAAGTCATTATTTCACTTACTTGTGACTTGTTGGGGATTATATATGTAATATTTGCATGCAATGCTGAAAATGGCATTTGTGATTTCCAGTCTTTAGTGATATTGCATAATTTATTTTTTCAGTTAGACAAAGGCATAAGTATTTACGACTTTTTCTTAATGGAACATTCGGAGAATAAT... |
Task1_train_41169 | A mutation has occurred on Chromosome 11. What is the medical relevance of this mutation? | Benign | AATTCAAATAATCACTGTGACCTAATTCTTCCTTATTATAATCTATTCACACTGTCCTCCATTAAGACCCCCTACCCCCTCAAAAACTAAATGCTTTAACTTATTTTCTACCTCATACCAGTATTTTCAGCATATACATTCTCCACTAGAATCCTTGAATGTTCTTCCTATGATTCATTAAACATCTGGTTCTTTCAGATCCTTTAGGTCTCAATACAGATGTCACCTTCTCAAGAAGGGCTTCCCATCTTAAAATAAAAGTTGAAGAAAAAGAAATTAAAACTAAAAAGAAACTGCTAAAATTAAAAAAGACCTTCCCA... | AATTCAAATAATCACTGTGACCTAATTCTTCCTTATTATAATCTATTCACACTGTCCTCCATTAAGACCCCCTACCCCCTCAAAAACTAAATGCTTTAACTTATTTTCTACCTCATACCAGTATTTTCAGCATATACATTCTCCACTAGAATCCTTGAATGTTCTTCCTATGATTCATTAAACATCTGGTTCTTTCAGATCCTTTAGGTCTCAATACAGATGTCACCTTCTCAAGAAGGGCTTCCCATCTTAAAATAAAAGTTGAAGAAAAAGAAATTAAAACTAAAAAGAAACTGCTAAAATTAAAAAAGACCTTCCCA... |
Task1_train_41170 | Assess the clinical impact of this variant found on Chromosome 11. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | AGAAGGGCTTCCCATCTTAAAATAAAAGTTGAAGAAAAAGAAATTAAAACTAAAAAGAAACTGCTAAAATTAAAAAAGACCTTCCCATAACATACCATGTGAAAATATTCTCCCAAGTTGTCATAATGTATCTTCATATTTAATTTCCTTATTTATTATTGAAATGTGCAATAATCTTGTTTCTACATTTCTTTACCAGATTTTTGTATGTTTCCTTTCATTGGAATAGTAGGTCCATAAAACAAGGGATAACTAGTTTATGTGAAGTTTGCACGTTACCAGAGTAAGAATTCAATAAACAGGTGGTAAATAAATAAATA... | AGAAGGGCTTCCCATCTTAAAATAAAAGTTGAAGAAAAAGAAATTAAAACTAAAAAGAAACTGCTAAAATTAAAAAAGACCTTCCCATAACATACCATGTGAAAATATTCTCCCAAGTTGTCATAATGTATCTTCATATTTAATTTCCTTATTTATTATTGAAATGTGCAATAATCTTGTTTCTACATTTCTTTACCAGATTTTTGTATGTTTCCTTTCATTGGAATAGTAGGTCCATAAAACAAGGGATAACTAGTTTATGTGAAGTTTGCACGTTACCAGAGTAAGAATTCAATAAACAGGTGGTAAATAAATAAATA... |
Task1_train_41171 | Located on Chromosome 11, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | AAATAAAAGTTGAAGAAAAAGAAATTAAAACTAAAAAGAAACTGCTAAAATTAAAAAAGACCTTCCCATAACATACCATGTGAAAATATTCTCCCAAGTTGTCATAATGTATCTTCATATTTAATTTCCTTATTTATTATTGAAATGTGCAATAATCTTGTTTCTACATTTCTTTACCAGATTTTTGTATGTTTCCTTTCATTGGAATAGTAGGTCCATAAAACAAGGGATAACTAGTTTATGTGAAGTTTGCACGTTACCAGAGTAAGAATTCAATAAACAGGTGGTAAATAAATAAATAAGAAGATTATTTTGAAAAA... | AAATAAAAGTTGAAGAAAAAGAAATTAAAACTAAAAAGAAACTGCTAAAATTAAAAAAGACCTTCCCATAACATACCATGTGAAAATATTCTCCCAAGTTGTCATAATGTATCTTCATATTTAATTTCCTTATTTATTATTGAAATGTGCAATAATCTTGTTTCTACATTTCTTTACCAGATTTTTGTATGTTTCCTTTCATTGGAATAGTAGGTCCATAAAACAAGGGATAACTAGTTTATGTGAAGTTTGCACGTTACCAGAGTAAGAATTCAATAAACAGGTGGTAAATAAATAAATAAGAAGATTATTTTGAAAAA... |
Task1_train_41172 | Located on Chromosome 11, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | AAAAGTGTGATGTTTGGTTTGAGAATCAAACTGAGATCGGATATTAACAATGTTAGGAATTATTTTGGTTCATTTCATTCTTTTTTCACACTGCAGGATAGTTTTCTATTTTTCTTTTCATTGTATCTTTTTTTTTACAAGGAGACAAAATTTAAACAACGCTGGGATTTTAAAATTCAGGCATTTTAAATGATATAGTGTTAACTCTCTGTAACTTAACTCCACATTTTTAAATAAGTGACTATGACAGGATTTCTTTGGGCCAGGTGTCCACAACAGGGGAACTATAAATTGTAGCAGAGACTCCAGTTGGCTTAGTT... | AAAAGTGTGATGTTTGGTTTGAGAATCAAACTGAGATCGGATATTAACAATGTTAGGAATTATTTTGGTTCATTTCATTCTTTTTTCACACTGCAGGATAGTTTTCTATTTTTCTTTTCATTGTATCTTTTTTTTTACAAGGAGACAAAATTTAAACAACGCTGGGATTTTAAAATTCAGGCATTTTAAATGATATAGTGTTAACTCTCTGTAACTTAACTCCACATTTTTAAATAAGTGACTATGACAGGATTTCTTTGGGCCAGGTGTCCACAACAGGGGAACTATAAATTGTAGCAGAGACTCCAGTTGGCTTAGTT... |
Task1_train_41173 | Given this context: Chromosome 11 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | ACCTAGTGGGAGTTTATCGGACCATGGGTGTGGTTTCCCCCATACTGTTTTCATGATAGTGAGTTAGTTCTCGCAAGATCTTATGGTTTCATAAGTGTTTGACAGCTCCTCCTTTGCATGTACATTCTCTCCTGCTGCCTTGTAAAGAAAGTGCCTGCTTCCTCTTCCACCATCATTGTAAATTACCCAGTCTTGAGTAGTATCTTTACAGCAATGTGAGAATGGACTAATACAGTGACAAAGCATATAAGTGTGTAAGCTTCAAAGCATCAAGGGAGTTGACACAAATGCAAGATATAATTATCAATATGCAGCAATTT... | ACCTAGTGGGAGTTTATCGGACCATGGGTGTGGTTTCCCCCATACTGTTTTCATGATAGTGAGTTAGTTCTCGCAAGATCTTATGGTTTCATAAGTGTTTGACAGCTCCTCCTTTGCATGTACATTCTCTCCTGCTGCCTTGTAAAGAAAGTGCCTGCTTCCTCTTCCACCATCATTGTAAATTACCCAGTCTTGAGTAGTATCTTTACAGCAATGTGAGAATGGACTAATACAGTGACAAAGCATATAAGTGTGTAAGCTTCAAAGCATCAAGGGAGTTGACACAAATGCAAGATATAATTATCAATATGCAGCAATTT... |
Task1_train_41174 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | GGTTTCAATTCAGCACAGCAATGTAAGCACTGAAAAGAGTAAGAGCCAGGAGAGGTAAGGATTAGAGATTACAATTTAGACAGGCAATGGAAGAACACTTCAAAATATTCCAAAAAAGATTAAGCTCCTACAATCATCAATATGAAGAGATTACTCACAGGCTTCTGCAGAGTAAGCCTCAATCTAAATAATATTAACGCTATCAAGAGCTAAAATTGATTTATTTGGCAAACAGTATGAGATAGTCACTACCTGAAGCACTTGGCATGGACGAATTCATTGATTGCTTTATCAAAGTTGCCTTGATCTCTTGTTGATGC... | GGTTTCAATTCAGCACAGCAATGTAAGCACTGAAAAGAGTAAGAGCCAGGAGAGGTAAGGATTAGAGATTACAATTTAGACAGGCAATGGAAGAACACTTCAAAATATTCCAAAAAAGATTAAGCTCCTACAATCATCAATATGAAGAGATTACTCACAGGCTTCTGCAGAGTAAGCCTCAATCTAAATAATATTAACGCTATCAAGAGCTAAAATTGATTTATTTGGCAAACAGTATGAGATAGTCACTACCTGAAGCACTTGGCATGGACGAATTCATTGATTGCTTTATCAAAGTTGCCTTGATCTCTTGTTGATGC... |
Task1_train_41175 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | TGAAAAGAGTAAGAGCCAGGAGAGGTAAGGATTAGAGATTACAATTTAGACAGGCAATGGAAGAACACTTCAAAATATTCCAAAAAAGATTAAGCTCCTACAATCATCAATATGAAGAGATTACTCACAGGCTTCTGCAGAGTAAGCCTCAATCTAAATAATATTAACGCTATCAAGAGCTAAAATTGATTTATTTGGCAAACAGTATGAGATAGTCACTACCTGAAGCACTTGGCATGGACGAATTCATTGATTGCTTTATCAAAGTTGCCTTGATCTCTTGTTGATGCAGAAATTTTTGCCTTTCTGATAATTTGCAT... | TGAAAAGAGTAAGAGCCAGGAGAGGTAAGGATTAGAGATTACAATTTAGACAGGCAATGGAAGAACACTTCAAAATATTCCAAAAAAGATTAAGCTCCTACAATCATCAATATGAAGAGATTACTCACAGGCTTCTGCAGAGTAAGCCTCAATCTAAATAATATTAACGCTATCAAGAGCTAAAATTGATTTATTTGGCAAACAGTATGAGATAGTCACTACCTGAAGCACTTGGCATGGACGAATTCATTGATTGCTTTATCAAAGTTGCCTTGATCTCTTGTTGATGCAGAAATTTTTGCCTTTCTGATAATTTGCAT... |
Task1_train_41176 | A genetic alteration is present on Chromosome 11. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TAAGCCTCAATCTAAATAATATTAACGCTATCAAGAGCTAAAATTGATTTATTTGGCAAACAGTATGAGATAGTCACTACCTGAAGCACTTGGCATGGACGAATTCATTGATTGCTTTATCAAAGTTGCCTTGATCTCTTGTTGATGCAGAAATTTTTGCCTTTCTGATAATTTGCATCAACTATGGATTGAGGTTAGGGAGTCACAGACTAGGTAATGAGTTATTCTGCTTCACCTTATGCCAGTCATGAAGCATGAAGAGGGCTTAAGTTCTCAGCTTCAGTTTCTATATGTGAAAATAAAGATGATAGTCATAGGGC... | TAAGCCTCAATCTAAATAATATTAACGCTATCAAGAGCTAAAATTGATTTATTTGGCAAACAGTATGAGATAGTCACTACCTGAAGCACTTGGCATGGACGAATTCATTGATTGCTTTATCAAAGTTGCCTTGATCTCTTGTTGATGCAGAAATTTTTGCCTTTCTGATAATTTGCATCAACTATGGATTGAGGTTAGGGAGTCACAGACTAGGTAATGAGTTATTCTGCTTCACCTTATGCCAGTCATGAAGCATGAAGAGGGCTTAAGTTCTCAGCTTCAGTTTCTATATGTGAAAATAAAGATGATAGTCATAGGGC... |
Task1_train_41177 | A variant found on Chromosome 11 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GATTGCTTTATCAAAGTTGCCTTGATCTCTTGTTGATGCAGAAATTTTTGCCTTTCTGATAATTTGCATCAACTATGGATTGAGGTTAGGGAGTCACAGACTAGGTAATGAGTTATTCTGCTTCACCTTATGCCAGTCATGAAGCATGAAGAGGGCTTAAGTTCTCAGCTTCAGTTTCTATATGTGAAAATAAAGATGATAGTCATAGGGCCATTATATAGGCTAGATGTAAAGATAATCTAAGCTAGAATAATAACAAAAAATTAAATTTATATCACTTCTGTTCAAGTGAAGATCATTAAATGCTGGCTACTTTTAAT... | GATTGCTTTATCAAAGTTGCCTTGATCTCTTGTTGATGCAGAAATTTTTGCCTTTCTGATAATTTGCATCAACTATGGATTGAGGTTAGGGAGTCACAGACTAGGTAATGAGTTATTCTGCTTCACCTTATGCCAGTCATGAAGCATGAAGAGGGCTTAAGTTCTCAGCTTCAGTTTCTATATGTGAAAATAAAGATGATAGTCATAGGGCCATTATATAGGCTAGATGTAAAGATAATCTAAGCTAGAATAATAACAAAAAATTAAATTTATATCACTTCTGTTCAAGTGAAGATCATTAAATGCTGGCTACTTTTAAT... |
Task1_train_41178 | A mutation on Chromosome 11 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CAGAAGGGTGACAAATACAAGTATTTATTTAAATATGCCTGGAGACTGAATAGTGTTTATTTCAATGTTTTGTCTGAAGGACTGGTGTTTTAGGAGATGAACTCAGTGACCTGGAGCAATTTTCAGATGATAGTTTTAGAGGCTGCACAGAACTGCGTGTATCTGCGCAAGAATAAACATTTAAAAAAAAAAGTCTATTGAGTAAAGTTGAATTTCTTAGCTCATTTCCCTTAGAAAACCTAGGTTTATCTCAATATGTGATTGTTAATAGTAGGGAATTATAACTCTGTAAAGACATGAAGAATTCAATTAATGTTTAA... | CAGAAGGGTGACAAATACAAGTATTTATTTAAATATGCCTGGAGACTGAATAGTGTTTATTTCAATGTTTTGTCTGAAGGACTGGTGTTTTAGGAGATGAACTCAGTGACCTGGAGCAATTTTCAGATGATAGTTTTAGAGGCTGCACAGAACTGCGTGTATCTGCGCAAGAATAAACATTTAAAAAAAAAAGTCTATTGAGTAAAGTTGAATTTCTTAGCTCATTTCCCTTAGAAAACCTAGGTTTATCTCAATATGTGATTGTTAATAGTAGGGAATTATAACTCTGTAAAGACATGAAGAATTCAATTAATGTTTAA... |
Task1_train_41179 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | TAATTCTATCAAGTAGGCAGGTGCAGTGAAACCACAGAAGACCAATCTCCTCCAGGTGAATTTTCAGGATCCGTAGACCTGAATCTCACTACCTGTAAAAAGAGAGACTGTCTATGACTCTTGTCGTGGCTCTGATATGTGAGAATATTGTGTATATCCATCCACAGAAATATACACTCACAAGACAAAGTGTGGAGAGTAGAAAAACCAGGTTTCTCTGTTAAACCTGTTTTAAAGGCCAGGTAATTCACTCCACTCACAAGGTTCTAAAAGCACCTCAGGGTAGCATATCTGAGTCATTTACAAAGAAAGTACAGAAG... | TAATTCTATCAAGTAGGCAGGTGCAGTGAAACCACAGAAGACCAATCTCCTCCAGGTGAATTTTCAGGATCCGTAGACCTGAATCTCACTACCTGTAAAAAGAGAGACTGTCTATGACTCTTGTCGTGGCTCTGATATGTGAGAATATTGTGTATATCCATCCACAGAAATATACACTCACAAGACAAAGTGTGGAGAGTAGAAAAACCAGGTTTCTCTGTTAAACCTGTTTTAAAGGCCAGGTAATTCACTCCACTCACAAGGTTCTAAAAGCACCTCAGGGTAGCATATCTGAGTCATTTACAAAGAAAGTACAGAAG... |
Task1_train_41180 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GAGACTGTCTATGACTCTTGTCGTGGCTCTGATATGTGAGAATATTGTGTATATCCATCCACAGAAATATACACTCACAAGACAAAGTGTGGAGAGTAGAAAAACCAGGTTTCTCTGTTAAACCTGTTTTAAAGGCCAGGTAATTCACTCCACTCACAAGGTTCTAAAAGCACCTCAGGGTAGCATATCTGAGTCATTTACAAAGAAAGTACAGAAGAGGAAATAATCACAGTATATTGTAAAGCTCAAATTGTATTTTATATAATGGCTGCAAGTATCATAATCTCCTTGTAAAATTGAAAAAAAATAATAATTTTAAA... | GAGACTGTCTATGACTCTTGTCGTGGCTCTGATATGTGAGAATATTGTGTATATCCATCCACAGAAATATACACTCACAAGACAAAGTGTGGAGAGTAGAAAAACCAGGTTTCTCTGTTAAACCTGTTTTAAAGGCCAGGTAATTCACTCCACTCACAAGGTTCTAAAAGCACCTCAGGGTAGCATATCTGAGTCATTTACAAAGAAAGTACAGAAGAGGAAATAATCACAGTATATTGTAAAGCTCAAATTGTATTTTATATAATGGCTGCAAGTATCATAATCTCCTTGTAAAATTGAAAAAAAATAATAATTTTAAA... |
Task1_train_41181 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | TGTCGTGGCTCTGATATGTGAGAATATTGTGTATATCCATCCACAGAAATATACACTCACAAGACAAAGTGTGGAGAGTAGAAAAACCAGGTTTCTCTGTTAAACCTGTTTTAAAGGCCAGGTAATTCACTCCACTCACAAGGTTCTAAAAGCACCTCAGGGTAGCATATCTGAGTCATTTACAAAGAAAGTACAGAAGAGGAAATAATCACAGTATATTGTAAAGCTCAAATTGTATTTTATATAATGGCTGCAAGTATCATAATCTCCTTGTAAAATTGAAAAAAAATAATAATTTTAAACCACTACTTTTTCTGAAA... | TGTCGTGGCTCTGATATGTGAGAATATTGTGTATATCCATCCACAGAAATATACACTCACAAGACAAAGTGTGGAGAGTAGAAAAACCAGGTTTCTCTGTTAAACCTGTTTTAAAGGCCAGGTAATTCACTCCACTCACAAGGTTCTAAAAGCACCTCAGGGTAGCATATCTGAGTCATTTACAAAGAAAGTACAGAAGAGGAAATAATCACAGTATATTGTAAAGCTCAAATTGTATTTTATATAATGGCTGCAAGTATCATAATCTCCTTGTAAAATTGAAAAAAAATAATAATTTTAAACCACTACTTTTTCTGAAA... |
Task1_train_41182 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TCGTGGCTCTGATATGTGAGAATATTGTGTATATCCATCCACAGAAATATACACTCACAAGACAAAGTGTGGAGAGTAGAAAAACCAGGTTTCTCTGTTAAACCTGTTTTAAAGGCCAGGTAATTCACTCCACTCACAAGGTTCTAAAAGCACCTCAGGGTAGCATATCTGAGTCATTTACAAAGAAAGTACAGAAGAGGAAATAATCACAGTATATTGTAAAGCTCAAATTGTATTTTATATAATGGCTGCAAGTATCATAATCTCCTTGTAAAATTGAAAAAAAATAATAATTTTAAACCACTACTTTTTCTGAAATG... | TCGTGGCTCTGATATGTGAGAATATTGTGTATATCCATCCACAGAAATATACACTCACAAGACAAAGTGTGGAGAGTAGAAAAACCAGGTTTCTCTGTTAAACCTGTTTTAAAGGCCAGGTAATTCACTCCACTCACAAGGTTCTAAAAGCACCTCAGGGTAGCATATCTGAGTCATTTACAAAGAAAGTACAGAAGAGGAAATAATCACAGTATATTGTAAAGCTCAAATTGTATTTTATATAATGGCTGCAAGTATCATAATCTCCTTGTAAAATTGAAAAAAAATAATAATTTTAAACCACTACTTTTTCTGAAATG... |
Task1_train_41183 | Located on Chromosome 11, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TCACAAGACAAAGTGTGGAGAGTAGAAAAACCAGGTTTCTCTGTTAAACCTGTTTTAAAGGCCAGGTAATTCACTCCACTCACAAGGTTCTAAAAGCACCTCAGGGTAGCATATCTGAGTCATTTACAAAGAAAGTACAGAAGAGGAAATAATCACAGTATATTGTAAAGCTCAAATTGTATTTTATATAATGGCTGCAAGTATCATAATCTCCTTGTAAAATTGAAAAAAAATAATAATTTTAAACCACTACTTTTTCTGAAATGTCAAAACAATAAAAATGTATCATATCACTTTTTTTAATCATATGTCATCATCTA... | TCACAAGACAAAGTGTGGAGAGTAGAAAAACCAGGTTTCTCTGTTAAACCTGTTTTAAAGGCCAGGTAATTCACTCCACTCACAAGGTTCTAAAAGCACCTCAGGGTAGCATATCTGAGTCATTTACAAAGAAAGTACAGAAGAGGAAATAATCACAGTATATTGTAAAGCTCAAATTGTATTTTATATAATGGCTGCAAGTATCATAATCTCCTTGTAAAATTGAAAAAAAATAATAATTTTAAACCACTACTTTTTCTGAAATGTCAAAACAATAAAAATGTATCATATCACTTTTTTTAATCATATGTCATCATCTA... |
Task1_train_41184 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | TATCACTTTTTTTAATCATATGTCATCATCTACAAGGGTGACTGAATAAATAGCAGGCACAAATAAATTACATAATAACATAGGGTACTTTCTAATTGAACAAATATGCAAGTACAATGAAGGTGTTTATTTTAAAAATTATTTCTTATAAAACATGTTCTTCCAATTATATTTTTTAAAAAATCTGATAATGACACATTTAAATCCAATTAACCTCATTCTTAACACCCACAGTGTTAACAAAAAATTCAGATAAACCTAAATTTGCTTTTAGAATTTTCATATTGCTAGTTATGTGACCTTCAATTTAGAGAGAAAAC... | TATCACTTTTTTTAATCATATGTCATCATCTACAAGGGTGACTGAATAAATAGCAGGCACAAATAAATTACATAATAACATAGGGTACTTTCTAATTGAACAAATATGCAAGTACAATGAAGGTGTTTATTTTAAAAATTATTTCTTATAAAACATGTTCTTCCAATTATATTTTTTAAAAAATCTGATAATGACACATTTAAATCCAATTAACCTCATTCTTAACACCCACAGTGTTAACAAAAAATTCAGATAAACCTAAATTTGCTTTTAGAATTTTCATATTGCTAGTTATGTGACCTTCAATTTAGAGAGAAAAC... |
Task1_train_41185 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | AAACTTAGACATGAGCCCCTCAAATGTAATAAAAACTGAAAACATATTGAATGAACTGGAAAGAGGACCCAGAGTCTCAGGTGGAACCACAGACCTGACCAAGAAATTGATTTCTGCCTGAGAAGACCCTGAGCAGCAGGCCCATTTTATCTTTACCTGCACTCATAACCCATGGCAATTCTGAAATAATAAATTTATGCTGTTTAAGTTGTTAAAACAAAAAAGCCCAAACCCCCACAAATGTATATCAGGATAATAAGGAGAGATTAGAACTCTGACATACAGTTGGATAGCAAGTTTTATATTTCTAAAAGGAAAAA... | AAACTTAGACATGAGCCCCTCAAATGTAATAAAAACTGAAAACATATTGAATGAACTGGAAAGAGGACCCAGAGTCTCAGGTGGAACCACAGACCTGACCAAGAAATTGATTTCTGCCTGAGAAGACCCTGAGCAGCAGGCCCATTTTATCTTTACCTGCACTCATAACCCATGGCAATTCTGAAATAATAAATTTATGCTGTTTAAGTTGTTAAAACAAAAAAGCCCAAACCCCCACAAATGTATATCAGGATAATAAGGAGAGATTAGAACTCTGACATACAGTTGGATAGCAAGTTTTATATTTCTAAAAGGAAAAA... |
Task1_train_41186 | Mutation context: Chromosome 11. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TGAACTGGAAAGAGGACCCAGAGTCTCAGGTGGAACCACAGACCTGACCAAGAAATTGATTTCTGCCTGAGAAGACCCTGAGCAGCAGGCCCATTTTATCTTTACCTGCACTCATAACCCATGGCAATTCTGAAATAATAAATTTATGCTGTTTAAGTTGTTAAAACAAAAAAGCCCAAACCCCCACAAATGTATATCAGGATAATAAGGAGAGATTAGAACTCTGACATACAGTTGGATAGCAAGTTTTATATTTCTAAAAGGAAAAATGAACTAGTGGAGAATGAGGAATAGCTCTGCCATAATGACCCCCCAAAAAA... | TGAACTGGAAAGAGGACCCAGAGTCTCAGGTGGAACCACAGACCTGACCAAGAAATTGATTTCTGCCTGAGAAGACCCTGAGCAGCAGGCCCATTTTATCTTTACCTGCACTCATAACCCATGGCAATTCTGAAATAATAAATTTATGCTGTTTAAGTTGTTAAAACAAAAAAGCCCAAACCCCCACAAATGTATATCAGGATAATAAGGAGAGATTAGAACTCTGACATACAGTTGGATAGCAAGTTTTATATTTCTAAAAGGAAAAATGAACTAGTGGAGAATGAGGAATAGCTCTGCCATAATGACCCCCCAAAAAA... |
Task1_train_41187 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | GGAGAGATTAGAACTCTGACATACAGTTGGATAGCAAGTTTTATATTTCTAAAAGGAAAAATGAACTAGTGGAGAATGAGGAATAGCTCTGCCATAATGACCCCCCAAAAAATAAGGCCTTAGAATGTCAGGTTGTGACGCCGATCTCTGTAAAAGAAGTTGTTGCTTGAGTAGCCCTGCGTTTTGTTCTTCATCCTGACTTTTTAGAAGCAAATTTGGGTGGTTTAGAAATATAAACATAGTGTTAACACAATTTTCAATACAAGCAGATCATACTTTACTTTCAGAATGTAAATTTATGAAAGAGTACGTATCCCATC... | GGAGAGATTAGAACTCTGACATACAGTTGGATAGCAAGTTTTATATTTCTAAAAGGAAAAATGAACTAGTGGAGAATGAGGAATAGCTCTGCCATAATGACCCCCCAAAAAATAAGGCCTTAGAATGTCAGGTTGTGACGCCGATCTCTGTAAAAGAAGTTGTTGCTTGAGTAGCCCTGCGTTTTGTTCTTCATCCTGACTTTTTAGAAGCAAATTTGGGTGGTTTAGAAATATAAACATAGTGTTAACACAATTTTCAATACAAGCAGATCATACTTTACTTTCAGAATGTAAATTTATGAAAGAGTACGTATCCCATC... |
Task1_train_41188 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | AGGAAAGTGAACCATGGTAAATTTGCATGAATAACAATGCTTTCTGTGTTTGAATTAGTCCATCTTCCTACAAGCATTACCACAACTATATTTTACTTCTCAGAGTCAACTTGTACATACTAATTGAATTGTGCACCCTTGTAGTTGGATTATCACATCCCGAATAAACTCACTCATCAGCAATCACCTTTATCTCCCACTTGCCTTTATGCAGTTAACTTAGCAAGAGTCACCTGGGGCAAACAAATTTCCATTGTTGTCTTTAACAAGAATATAATGTAGAACAAGTAAGCTATGGAAGCACCAATCTAGACAAACAG... | AGGAAAGTGAACCATGGTAAATTTGCATGAATAACAATGCTTTCTGTGTTTGAATTAGTCCATCTTCCTACAAGCATTACCACAACTATATTTTACTTCTCAGAGTCAACTTGTACATACTAATTGAATTGTGCACCCTTGTAGTTGGATTATCACATCCCGAATAAACTCACTCATCAGCAATCACCTTTATCTCCCACTTGCCTTTATGCAGTTAACTTAGCAAGAGTCACCTGGGGCAAACAAATTTCCATTGTTGTCTTTAACAAGAATATAATGTAGAACAAGTAAGCTATGGAAGCACCAATCTAGACAAACAG... |
Task1_train_41189 | A genomic variant on Chromosome 11 is under review. What is the biological outcome — benign or pathogenic? | Benign | TGCTTTTCTCTCAGATGACACCAATCTTGCTTTATATTCACATCTTTGCAGATAATTTTAATTATTTAAATGTATAATATAAAATGTATAAATTACATTTCTTTAGCTATATATTGTTTGCCTCAAAACAGAAGGTGATTATTTATTTATTTGGGCTGAGGACGTAGACTTGATGAAATAAGTTAAGTTGTAGCTTCATCCTTATGCTTCACGAAATATGGTGCAAGAGAGATGTGAAATTATGTTCCCATTATTATGTCATAAAATGTTATTGATAACAACAAATAGTGCATGCTAAATACTGAATTTATTTTAAATGC... | TGCTTTTCTCTCAGATGACACCAATCTTGCTTTATATTCACATCTTTGCAGATAATTTTAATTATTTAAATGTATAATATAAAATGTATAAATTACATTTCTTTAGCTATATATTGTTTGCCTCAAAACAGAAGGTGATTATTTATTTATTTGGGCTGAGGACGTAGACTTGATGAAATAAGTTAAGTTGTAGCTTCATCCTTATGCTTCACGAAATATGGTGCAAGAGAGATGTGAAATTATGTTCCCATTATTATGTCATAAAATGTTATTGATAACAACAAATAGTGCATGCTAAATACTGAATTTATTTTAAATGC... |
Task1_train_41190 | A mutation on Chromosome 11 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | ACTTGAACATTTTATAGTAGATACAGTAGTTGATATCATATAAGCATTTTCTGTAGCATTTTCTGTATAGTGTTAGTTAAAAGCAGAGTGCAAAATATTAAAATGTCAAACATAAGAGGCAATTTAATAGGGCTAAATATGTATGTATTAATATGCAGTCATCTGGTTGACTAAATAATACATTGATTAATGTGTATCTTTATTTAGCCTCTTTGTGATTGATTTTCCCTGTAGTAGCTTTGAGAACTAGAATACCCTAATGTAAAAAAATAATGTGCCACAGACAGTTGTGTGAAGCAAAATAAACACTATTTCCTCCA... | ACTTGAACATTTTATAGTAGATACAGTAGTTGATATCATATAAGCATTTTCTGTAGCATTTTCTGTATAGTGTTAGTTAAAAGCAGAGTGCAAAATATTAAAATGTCAAACATAAGAGGCAATTTAATAGGGCTAAATATGTATGTATTAATATGCAGTCATCTGGTTGACTAAATAATACATTGATTAATGTGTATCTTTATTTAGCCTCTTTGTGATTGATTTTCCCTGTAGTAGCTTTGAGAACTAGAATACCCTAATGTAAAAAAATAATGTGCCACAGACAGTTGTGTGAAGCAAAATAAACACTATTTCCTCCA... |
Task1_train_41191 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GAGGGTGCATTCCTCCACTTGCTTTCTGGGAACACCTTACTCTGTAATGCAATAGCCTTTAATAAATGATCTCTTTGGAGTAGCATTTAATGAACTATCTCTTCTCACTGCACTTTGCAGCTTATCTTGAAATTTTTCCTCTGTAGATCCAAGAACCCCCTGCTGGGATCTGGATCAAGACCCCTTTTTCCACTAACAAAGTCATTTATGCATATGCAAATATCAATTGATAAACCCTATTGATTCCTACTAAATTATTCCTAAGTCAGAGGTACTTCACTGGAAAACATACGTGGAATGCAATTGAAGTATTTTGATGA... | GAGGGTGCATTCCTCCACTTGCTTTCTGGGAACACCTTACTCTGTAATGCAATAGCCTTTAATAAATGATCTCTTTGGAGTAGCATTTAATGAACTATCTCTTCTCACTGCACTTTGCAGCTTATCTTGAAATTTTTCCTCTGTAGATCCAAGAACCCCCTGCTGGGATCTGGATCAAGACCCCTTTTTCCACTAACAAAGTCATTTATGCATATGCAAATATCAATTGATAAACCCTATTGATTCCTACTAAATTATTCCTAAGTCAGAGGTACTTCACTGGAAAACATACGTGGAATGCAATTGAAGTATTTTGATGA... |
Task1_train_41192 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TCTCATTATTTCATTTATGAAGATTAAAATAAAGTGTTCCTAAAATCAGCACTACACTGTGACTGCAACTCTTATAATTACTTTTATTCATGTCGATTTATGTTCTATCCTATCTCCAAAGAATTTCTGAGGTGACTTTTACCCAAAGACATGCAGAAGGAAAAAATTAAATCACAAATAGAAATAAATAAAATATTTTATTAAAAATCAATTAGAAACAGGTCAGTCATTTTGACTAAAAGGATGTCAAAGTTTAAAAATGGTTGCTGCAAGCCAGAGCAATTCTCATAACTAGAAAATAAATGGAATCGTACAGTTAT... | TCTCATTATTTCATTTATGAAGATTAAAATAAAGTGTTCCTAAAATCAGCACTACACTGTGACTGCAACTCTTATAATTACTTTTATTCATGTCGATTTATGTTCTATCCTATCTCCAAAGAATTTCTGAGGTGACTTTTACCCAAAGACATGCAGAAGGAAAAAATTAAATCACAAATAGAAATAAATAAAATATTTTATTAAAAATCAATTAGAAACAGGTCAGTCATTTTGACTAAAAGGATGTCAAAGTTTAAAAATGGTTGCTGCAAGCCAGAGCAATTCTCATAACTAGAAAATAAATGGAATCGTACAGTTAT... |
Task1_train_41193 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TAGAACTAGACATTTACCTAACTCCAAATCATTACACAGACTTCCTTCAACATGTCATCTCATCACAGAAGGCTGTTGTCTCATTGCTCCAACATTGAGAGTTTCCTCCTCACTATGATAAGCAATACAGATACAATTTTCTTTGATAAGTATTTATTGAAAATTATGTGAACCTTTAGGAAGAGCAGAGATAAAACGTTGAAGTACATTGATTACTACCAACAAAATATTCAGTTTAATTCAAAAGTCAGTAAAATATTCCCCCATTATTCTTGTGGTTCCCACAATATCATAATACCTGATAAGACTTATTCATCTAT... | TAGAACTAGACATTTACCTAACTCCAAATCATTACACAGACTTCCTTCAACATGTCATCTCATCACAGAAGGCTGTTGTCTCATTGCTCCAACATTGAGAGTTTCCTCCTCACTATGATAAGCAATACAGATACAATTTTCTTTGATAAGTATTTATTGAAAATTATGTGAACCTTTAGGAAGAGCAGAGATAAAACGTTGAAGTACATTGATTACTACCAACAAAATATTCAGTTTAATTCAAAAGTCAGTAAAATATTCCCCCATTATTCTTGTGGTTCCCACAATATCATAATACCTGATAAGACTTATTCATCTAT... |
Task1_train_41194 | A mutation found on Chromosome 11 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AAAGTCTGAATTGCCATAATGTTCTCAAATCAATGCTAAGTGATGACAAACTGCTCAGAGAGGTTACAGAACTGGATTTTTATTTCTTTTTTACCATTGAACAAAATTCAACAAGAAAAATTGTGTTTCTTTGTGTTTCGTTTGTTTGTTATGATTTTGAGATCAGACTATAATATATACTACAGTATTGTAGATTCAATTGAATACTGATACAGTTTTTAAAATTCAGTATCTCCGATTAATGCAAAATGGAAAAGTAATTATTCTGATATCCTAAAGTGAAATTAAATTTTTACGATGTTCTTTCCCATAATATTGAC... | AAAGTCTGAATTGCCATAATGTTCTCAAATCAATGCTAAGTGATGACAAACTGCTCAGAGAGGTTACAGAACTGGATTTTTATTTCTTTTTTACCATTGAACAAAATTCAACAAGAAAAATTGTGTTTCTTTGTGTTTCGTTTGTTTGTTATGATTTTGAGATCAGACTATAATATATACTACAGTATTGTAGATTCAATTGAATACTGATACAGTTTTTAAAATTCAGTATCTCCGATTAATGCAAAATGGAAAAGTAATTATTCTGATATCCTAAAGTGAAATTAAATTTTTACGATGTTCTTTCCCATAATATTGAC... |
Task1_train_41195 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GTAAAGACAAATGAAATGGCTACAACTATTTGTCCTAAATTTTCAAAATTTAATTAATTTTTTAAATGTGCTAATTCCAGCAAATGTTATAACCTTTCCTCAACAAAGTTGCTAACCTCTGAGCTGCAAGCTTGTGATTTGAAAATTGTAACCATTAATCCTTAACTTGCCATCTTCTAAAGGCTACTAAATGAAATATCAACCCAACCTGCCATCACAAGGGGGTTCAGTTATGGAGTTTATATCAGGGTTTAGGGAATTGGGCTCGAGGCCAAGGCTAGTTTCCATGTGGTTAGCAACATGTTTGATTTTTCAGGGTT... | GTAAAGACAAATGAAATGGCTACAACTATTTGTCCTAAATTTTCAAAATTTAATTAATTTTTTAAATGTGCTAATTCCAGCAAATGTTATAACCTTTCCTCAACAAAGTTGCTAACCTCTGAGCTGCAAGCTTGTGATTTGAAAATTGTAACCATTAATCCTTAACTTGCCATCTTCTAAAGGCTACTAAATGAAATATCAACCCAACCTGCCATCACAAGGGGGTTCAGTTATGGAGTTTATATCAGGGTTTAGGGAATTGGGCTCGAGGCCAAGGCTAGTTTCCATGTGGTTAGCAACATGTTTGATTTTTCAGGGTT... |
Task1_train_41196 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | TTGTGAGGTGCAACAAAAAGTGGATTTTATATGTCAATCGGCAATGACCAGCTCAGTGGTTGGACTGAGAAGAAGCTCTAAAGTGCTTCCCAAAACCAAACTTGCACCAAAAAAAGGTCATGGTTGACAGAGCAGGAGCACCATTATCTCAGACAAACACTGCTACTTTAAGTTCCAGCTCCCTTTCTAGCTTCACAGATTCCAAGGAATCACTTTCTCTTCTAACTACAAGCAGCCAGAAAAGAGCAGACAGTAAAACACAGATAACACAGCTCAGGTGCAGAGGAGGGTGGGGAGGAAGTCTCTTGGGTAACTGCCAA... | TTGTGAGGTGCAACAAAAAGTGGATTTTATATGTCAATCGGCAATGACCAGCTCAGTGGTTGGACTGAGAAGAAGCTCTAAAGTGCTTCCCAAAACCAAACTTGCACCAAAAAAAGGTCATGGTTGACAGAGCAGGAGCACCATTATCTCAGACAAACACTGCTACTTTAAGTTCCAGCTCCCTTTCTAGCTTCACAGATTCCAAGGAATCACTTTCTCTTCTAACTACAAGCAGCCAGAAAAGAGCAGACAGTAAAACACAGATAACACAGCTCAGGTGCAGAGGAGGGTGGGGAGGAAGTCTCTTGGGTAACTGCCAA... |
Task1_train_41197 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | TCCTTTCAGGTCCACTAAGATAGGGAAGCTAAAGGCAGACTCGGGCGAGGTGCTTGCAGCTGCAGAAAGGTGTATGGGAACTGACACACAACTTTCCCTCCCAGATAAGCACAACAAAGAGACACAGAAGCAGTCCAAGCCTCTAATAAACTCTCCCACACTGAATCCTTAAAAACTCTTAGTCTGTAAGAGAGTGCAGCTTTTGACCTAACTCAGCCTGAAGTCCCTCCCATGTTTGTTTTCCGAAATAAACCATTAACTGTCAAGCCACCCTTTGTGTTTCTCTCCTCTTTATTTAATTCTTACAATGGTTGCTGTTA... | TCCTTTCAGGTCCACTAAGATAGGGAAGCTAAAGGCAGACTCGGGCGAGGTGCTTGCAGCTGCAGAAAGGTGTATGGGAACTGACACACAACTTTCCCTCCCAGATAAGCACAACAAAGAGACACAGAAGCAGTCCAAGCCTCTAATAAACTCTCCCACACTGAATCCTTAAAAACTCTTAGTCTGTAAGAGAGTGCAGCTTTTGACCTAACTCAGCCTGAAGTCCCTCCCATGTTTGTTTTCCGAAATAAACCATTAACTGTCAAGCCACCCTTTGTGTTTCTCTCCTCTTTATTTAATTCTTACAATGGTTGCTGTTA... |
Task1_train_41198 | This is a variant located on Chromosome 11. Is this mutation a likely cause of disease or not? | Benign | TATATTCACCTGAGCTCTCACCAATCAACTACCACTTCTTCGAACATCTTGACAACTTTTCGCAGGAAAAACACTTCCACAACAAGCAGGTTGCAGAAAATGCTTTCCAAGAGTTTATTGAATCTCAAAGCAGATTTTTTTTTTTCCGAGATGAAGTCTTGCTCTGTTGCCCAGGCTGGAATGCAGCGGTGTGATCTCAGATCACTGCAACCTCCACCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACGTCCCACCACACCTGGCTAATTTTTTGTATTTCTAATAGACACA... | TATATTCACCTGAGCTCTCACCAATCAACTACCACTTCTTCGAACATCTTGACAACTTTTCGCAGGAAAAACACTTCCACAACAAGCAGGTTGCAGAAAATGCTTTCCAAGAGTTTATTGAATCTCAAAGCAGATTTTTTTTTTTCCGAGATGAAGTCTTGCTCTGTTGCCCAGGCTGGAATGCAGCGGTGTGATCTCAGATCACTGCAACCTCCACCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACGTCCCACCACACCTGGCTAATTTTTTGTATTTCTAATAGACACA... |
Task1_train_41199 | Assess the clinical impact of this variant found on Chromosome 11. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | TGATGACTCCACACAGCTTTGTGTATTGGGCCCAAGACCATGGTGGCATGGGCTCATGAAGGGATCTCCTGATCTGTGGGATGCAGAGATCCATGAGAGAAGCGTGGTTTTCCAGGTGGGGTTGCAAAATCACTCACCACTTCCCTTAGCTGGAGATGGGGATTCTCTTGGCTCCATGCTGCTCCAGGGTGGGCCATCACCCCACCCCGCATTTTTTCACACTCCGTGGGTCAGGTTGTTTGCCTAGTCAGCCCCAGTATGAGAACCTGGATATTTCAGTTGAGGGTGCTGAATTCATTTGCCGCTTTCCTTCCGCTCTG... | TGATGACTCCACACAGCTTTGTGTATTGGGCCCAAGACCATGGTGGCATGGGCTCATGAAGGGATCTCCTGATCTGTGGGATGCAGAGATCCATGAGAGAAGCGTGGTTTTCCAGGTGGGGTTGCAAAATCACTCACCACTTCCCTTAGCTGGAGATGGGGATTCTCTTGGCTCCATGCTGCTCCAGGGTGGGCCATCACCCCACCCCGCATTTTTTCACACTCCGTGGGTCAGGTTGTTTGCCTAGTCAGCCCCAGTATGAGAACCTGGATATTTCAGTTGAGGGTGCTGAATTCATTTGCCGCTTTCCTTCCGCTCTG... |
Subsets and Splits
No community queries yet
The top public SQL queries from the community will appear here once available.