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_33200 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CACTGCAACCTCTGCCTCCCGGGTTCAAGGGATTCTCTTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATCCACCACCACTCCCGGCTAATTTTTTTGTATTTTTAGTAGAGATGGGGTTTTACCATGTTGGCCAGGCTGGTTTTGAACTCCTGACCTCAGGGGACCTGCCCACCTCGGCCTCTGAAAGTGCCAGGATTACAGGTGTGAGCCACCGCACCCGGCCACTTATTTATTTTTCAAGAAACTCCATGAATTAGGGATTTTAGCTCTCCATTTATTTGTCTGTCAAATTTATATATTTTTTGCCCATTAAA... | CACTGCAACCTCTGCCTCCCGGGTTCAAGGGATTCTCTTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATCCACCACCACTCCCGGCTAATTTTTTTGTATTTTTAGTAGAGATGGGGTTTTACCATGTTGGCCAGGCTGGTTTTGAACTCCTGACCTCAGGGGACCTGCCCACCTCGGCCTCTGAAAGTGCCAGGATTACAGGTGTGAGCCACCGCACCCGGCCACTTATTTATTTTTCAAGAAACTCCATGAATTAGGGATTTTAGCTCTCCATTTATTTGTCTGTCAAATTTATATATTTTTTGCCCATTAAA... |
Task1_train_33201 | A variant found on Chromosome 1 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | TATTTTTTCCTACCCATTTTCAATTGGAGTTGTCTTGTTGGAATATGTACCCTTTTAAGCACCTCAAGTTTCCTTTCAAACTGGACAGGCAATAGACACATAACTAATTTTTAACACTATTCACACATTTCTGTTAGACTGAAGCAGATTGTGCAGTGGAAATACTAGGCCTTTGGAGGGAGTCACACTTGGGTTTAAATTCCAGCTTTGACACTTAATAACTGTGGACCTTGGACAAATTATTTAACCTTTCTGAGTTCCCTCTCTGTAAAATGGAAATAATAATCCATAACTCACAAAGATGTCTTGGGGATTAAATA... | TATTTTTTCCTACCCATTTTCAATTGGAGTTGTCTTGTTGGAATATGTACCCTTTTAAGCACCTCAAGTTTCCTTTCAAACTGGACAGGCAATAGACACATAACTAATTTTTAACACTATTCACACATTTCTGTTAGACTGAAGCAGATTGTGCAGTGGAAATACTAGGCCTTTGGAGGGAGTCACACTTGGGTTTAAATTCCAGCTTTGACACTTAATAACTGTGGACCTTGGACAAATTATTTAACCTTTCTGAGTTCCCTCTCTGTAAAATGGAAATAATAATCCATAACTCACAAAGATGTCTTGGGGATTAAATA... |
Task1_train_33202 | Here is a genetic alteration on Chromosome 1. Based on the data, is it a benign variant or a cause of disease? | Benign | GCTCATGGGAGCCCCATGCCCAGGCCTCCTGGGCAAAGCCACAGAGGTCCTCAAGCCAGGCTGACTAGAAAGAGGTACAGAGGCATAATTGTGTTCCTGCAACTTCAGCCCTCAACTCCTTTCCCTCTACTTGAGAGCTCTCTGGTGGGGCAGGTTTGCCCTGAGGGCCACCATCCCACACTGTCTAGAGAGAGGCTTCTTCCTCTCCCTTCCTCTGTAATCATTACAAACAGTGGATATGACACAGTTCGTGCACTGGCTTCCCCTCTTGTGTCTAAAAGCTTGAGTCCTAAACAGCATTACACACTGCACACCATCTT... | GCTCATGGGAGCCCCATGCCCAGGCCTCCTGGGCAAAGCCACAGAGGTCCTCAAGCCAGGCTGACTAGAAAGAGGTACAGAGGCATAATTGTGTTCCTGCAACTTCAGCCCTCAACTCCTTTCCCTCTACTTGAGAGCTCTCTGGTGGGGCAGGTTTGCCCTGAGGGCCACCATCCCACACTGTCTAGAGAGAGGCTTCTTCCTCTCCCTTCCTCTGTAATCATTACAAACAGTGGATATGACACAGTTCGTGCACTGGCTTCCCCTCTTGTGTCTAAAAGCTTGAGTCCTAAACAGCATTACACACTGCACACCATCTT... |
Task1_train_33203 | Here is a genetic alteration on Chromosome 1. Based on the data, is it a benign variant or a cause of disease? | Benign | ACATGGGCCGCCACACTCCTTTTTTTTTATTTGTAGAGATGGGGTCTTACTATGTTGCCCAGGCTGGTCTCAAACTCCTAGCCTCAAGCAATTCTCCCACCTTGGCCTCCCAAACTGCTGAGATTATAGGTGTGGGCCCTAAATGTCCTTTAAGTGTTCTTCTAAGAGGGAGGCAAAGGGAAGTTTGACTACACAGAGAAGAAGGCAGCAGGGCAGGGAGAGATTCTGAAGATGCTAAGCTGCTGGCATCTAAGAGGAAGGGGACACGAGCGAAAGAATGCAAGGAATGCCGCTCTAGAAGCTGGAAAAGGATTCTCTCC... | ACATGGGCCGCCACACTCCTTTTTTTTTATTTGTAGAGATGGGGTCTTACTATGTTGCCCAGGCTGGTCTCAAACTCCTAGCCTCAAGCAATTCTCCCACCTTGGCCTCCCAAACTGCTGAGATTATAGGTGTGGGCCCTAAATGTCCTTTAAGTGTTCTTCTAAGAGGGAGGCAAAGGGAAGTTTGACTACACAGAGAAGAAGGCAGCAGGGCAGGGAGAGATTCTGAAGATGCTAAGCTGCTGGCATCTAAGAGGAAGGGGACACGAGCGAAAGAATGCAAGGAATGCCGCTCTAGAAGCTGGAAAAGGATTCTCTCC... |
Task1_train_33204 | This alteration on Chromosome 1 may affect genome function. Does it lead to a disease or is it benign? | Benign | TACCTTCTTCCAGTCAATCTGACAAATTGGACACTGTCACATACTCACACTGTGTTCTCCCAGCTCTGGGATTTCATCACGCTGACCTTCCCACTTGGGGTGCTCAGCATCCCCTGAATGTGCTTTCCTAAATCCTATTCATTCCTCTAGGCTCAGCTCAAATTTCACCTCCTCCCTGAAGATTTTGTGACCAGTCCAGTTCTTTCTTCTTTGAACTGATTGTCTTTAGCATACTCTTTAGCATCTGATTATCCTAATAAAGGTCCGTTCTCTCCCTGACCAGGCCATGCTGCTTGTCAGAGAAACCATGTCCTACACTT... | TACCTTCTTCCAGTCAATCTGACAAATTGGACACTGTCACATACTCACACTGTGTTCTCCCAGCTCTGGGATTTCATCACGCTGACCTTCCCACTTGGGGTGCTCAGCATCCCCTGAATGTGCTTTCCTAAATCCTATTCATTCCTCTAGGCTCAGCTCAAATTTCACCTCCTCCCTGAAGATTTTGTGACCAGTCCAGTTCTTTCTTCTTTGAACTGATTGTCTTTAGCATACTCTTTAGCATCTGATTATCCTAATAAAGGTCCGTTCTCTCCCTGACCAGGCCATGCTGCTTGTCAGAGAAACCATGTCCTACACTT... |
Task1_train_33205 | The following genetic variant occurs on Chromosome 1. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GATGAACATTTGGGTTGTCCAGCTTGGAGCTCTTATGAATAGTGCTACTCTCAAAATTCATCTACAAGGCTTTGTGGATATATATTTTCATTTTCCTAGAAGAATGGAATTGCTGGGTCCTATGATAAGTATAAGAAACTGTCAACCAGTTGTCCCACCAATAATGTATGAAAGTTCCAGCTGCTTCAGATCCTTGCCATATTTTATACCAATACACTAGAAAAATCTAAATGAGATAGACACTTTTTCTAGGAAAATATAATTACAAAAATTAGGTGAATAAAACTAAGAAAACTGAGAAGACTAATAACCATACAAAA... | GATGAACATTTGGGTTGTCCAGCTTGGAGCTCTTATGAATAGTGCTACTCTCAAAATTCATCTACAAGGCTTTGTGGATATATATTTTCATTTTCCTAGAAGAATGGAATTGCTGGGTCCTATGATAAGTATAAGAAACTGTCAACCAGTTGTCCCACCAATAATGTATGAAAGTTCCAGCTGCTTCAGATCCTTGCCATATTTTATACCAATACACTAGAAAAATCTAAATGAGATAGACACTTTTTCTAGGAAAATATAATTACAAAAATTAGGTGAATAAAACTAAGAAAACTGAGAAGACTAATAACCATACAAAA... |
Task1_train_33206 | This mutation is located on Chromosome 1. Is it associated with a disease or is it a benign polymorphism? | Benign | TGGGATACATGGCTTGGCTAATGAAGCACATATCCTTGTGCAGGGTGCAATCTACCCAACCACAGGCAACAGACCAGGTTGAGGCAGACAGCTCTTTCAGGAAGCTTAGCTGACAAGCGAGGGAGAAACAAGATGGGAGATGCAAAGGTGTCTCGGGCTGTGGATCAGTCCATGGATACCGGTCCTTCCCAATTCTGCTCTTTTCTGATGCTGACTGGCTCTGCCCAGGACCCTCTGCCCACTAACCCTCCTCCCATCAAAGATATCCTAAGCCTCCCTCCCTGGACCTCCGCCAGGCTAGAAGACCTGCTAGGACCTGT... | TGGGATACATGGCTTGGCTAATGAAGCACATATCCTTGTGCAGGGTGCAATCTACCCAACCACAGGCAACAGACCAGGTTGAGGCAGACAGCTCTTTCAGGAAGCTTAGCTGACAAGCGAGGGAGAAACAAGATGGGAGATGCAAAGGTGTCTCGGGCTGTGGATCAGTCCATGGATACCGGTCCTTCCCAATTCTGCTCTTTTCTGATGCTGACTGGCTCTGCCCAGGACCCTCTGCCCACTAACCCTCCTCCCATCAAAGATATCCTAAGCCTCCCTCCCTGGACCTCCGCCAGGCTAGAAGACCTGCTAGGACCTGT... |
Task1_train_33207 | Here’s a variant located on Chromosome 1. What is the predicted biological effect — harmless or disease-causing? | Benign | TGACACCACCCCGGCTCTGGCCCAAATACTACCCTCTTGAGGTCCAGGGTCTCATCAGAAGTGCACATCTGAGGCTAAGCCCCTAAACCACATATCTTAGGCTAGGCCACTGCACAGAGCTTAGACATGTGACACTGGGCTCAGATAGGCCATCGTGATAGGGCAGACCCCAGGGACCAACCCACACCTGTGTGATCCACACGAACATGGCACTTCAGAGCAGACAAGTGTAGGGCACCACATTTAGGAAAAATCTTCCTGCTGGGATTGTGCCTCTAACAAAGATGCCAGGGAAGGGTTCTAAAATGGCACAATCAGCC... | TGACACCACCCCGGCTCTGGCCCAAATACTACCCTCTTGAGGTCCAGGGTCTCATCAGAAGTGCACATCTGAGGCTAAGCCCCTAAACCACATATCTTAGGCTAGGCCACTGCACAGAGCTTAGACATGTGACACTGGGCTCAGATAGGCCATCGTGATAGGGCAGACCCCAGGGACCAACCCACACCTGTGTGATCCACACGAACATGGCACTTCAGAGCAGACAAGTGTAGGGCACCACATTTAGGAAAAATCTTCCTGCTGGGATTGTGCCTCTAACAAAGATGCCAGGGAAGGGTTCTAAAATGGCACAATCAGCC... |
Task1_train_33208 | A genetic alteration is present on Chromosome 1. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | CCGGCTCTGGCCCAAATACTACCCTCTTGAGGTCCAGGGTCTCATCAGAAGTGCACATCTGAGGCTAAGCCCCTAAACCACATATCTTAGGCTAGGCCACTGCACAGAGCTTAGACATGTGACACTGGGCTCAGATAGGCCATCGTGATAGGGCAGACCCCAGGGACCAACCCACACCTGTGTGATCCACACGAACATGGCACTTCAGAGCAGACAAGTGTAGGGCACCACATTTAGGAAAAATCTTCCTGCTGGGATTGTGCCTCTAACAAAGATGCCAGGGAAGGGTTCTAAAATGGCACAATCAGCCTCAAAATGTC... | CCGGCTCTGGCCCAAATACTACCCTCTTGAGGTCCAGGGTCTCATCAGAAGTGCACATCTGAGGCTAAGCCCCTAAACCACATATCTTAGGCTAGGCCACTGCACAGAGCTTAGACATGTGACACTGGGCTCAGATAGGCCATCGTGATAGGGCAGACCCCAGGGACCAACCCACACCTGTGTGATCCACACGAACATGGCACTTCAGAGCAGACAAGTGTAGGGCACCACATTTAGGAAAAATCTTCCTGCTGGGATTGTGCCTCTAACAAAGATGCCAGGGAAGGGTTCTAAAATGGCACAATCAGCCTCAAAATGTC... |
Task1_train_33209 | Chromosome 1 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GGTGCAGGCATGGAGGAGCTTCTGGCTTACCAGGAGAAGATGGGAGAATCACTGGCCCAGCCAGGGAAGGATGGGTATTTCCTTCAGCCTCCCTCTCTCAGGCCCTGGAGCATCCTCCCTGCCTGAATCTGATGGCTGAGATAGGCCCACTTATGACTAATCATTCCAGACTCCTCACTTCTATGGCACCTGCACAAACTATGTGCTCAGTAAAGAGTTGTTTGGATAAAGGAATGAGCCAACCAGTCCATCTTGGTGGATGATGAGGGGCTTTCTGCCTTCAGTCAGATGAACTTGAGCCAGCCTGAGAGAATGATCTT... | GGTGCAGGCATGGAGGAGCTTCTGGCTTACCAGGAGAAGATGGGAGAATCACTGGCCCAGCCAGGGAAGGATGGGTATTTCCTTCAGCCTCCCTCTCTCAGGCCCTGGAGCATCCTCCCTGCCTGAATCTGATGGCTGAGATAGGCCCACTTATGACTAATCATTCCAGACTCCTCACTTCTATGGCACCTGCACAAACTATGTGCTCAGTAAAGAGTTGTTTGGATAAAGGAATGAGCCAACCAGTCCATCTTGGTGGATGATGAGGGGCTTTCTGCCTTCAGTCAGATGAACTTGAGCCAGCCTGAGAGAATGATCTT... |
Task1_train_33210 | This variant is present on Chromosome 1. Is the change likely to result in a pathogenic outcome? | Benign | AGCCCGGATGAACTTCAGAGGCAAAGTAAACACCTTAAGTGCAGCATATTAAAACAGCACTTACCAAAGAAAACAAACAAACAAGAACACTACAAGGAAGCCACTGTCATTACATCATTTTCTCTTGTGTTTTCATTTCAGGGAAAGTCCTGGTCAGCAGCGAAATGGGCATCAGCCGGTCAGCAGTGCTGGTGGTCGCCTACCTGATGATCTTCCACAACATGGCCATCCTGGAGGCTTTGATGACCGTGCGTAAGAAGCGGGCCATCTACCCCAATGAGGGCTTCCTGAAGCAGCTGCGGGAGCTCAATGAGAAGTTG... | AGCCCGGATGAACTTCAGAGGCAAAGTAAACACCTTAAGTGCAGCATATTAAAACAGCACTTACCAAAGAAAACAAACAAACAAGAACACTACAAGGAAGCCACTGTCATTACATCATTTTCTCTTGTGTTTTCATTTCAGGGAAAGTCCTGGTCAGCAGCGAAATGGGCATCAGCCGGTCAGCAGTGCTGGTGGTCGCCTACCTGATGATCTTCCACAACATGGCCATCCTGGAGGCTTTGATGACCGTGCGTAAGAAGCGGGCCATCTACCCCAATGAGGGCTTCCTGAAGCAGCTGCGGGAGCTCAATGAGAAGTTG... |
Task1_train_33211 | Given this variant on Chromosome 1, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TCGAGGACGAGGACGTGGAGAGGATCATCCAGGAGTGGCAGAGCCGAAACGAGAGGTACCAAGCAGAAGGGTACCGGAGGTGGGGAAGGGAGGAGGAGAAGGAGGAGGAGAGCGACGCTGGCTCCTCGGTGGGGAGGCGGCGGCGCACCCTGAGCGAGAGCAGCGCCTGGGAGAGCGTGAGCAGCCACGACATCTGGGTCCTGAAGCAGCAGCTGGAGCTGAACCGCCCGGACCACGGCAGGAGGCGCCGCGCAGACTCGATGTCCTCGGAGAGCACCTGGGACGCATGGAACGAGAGGCTGCTGGAGATTGAGAAGGAG... | TCGAGGACGAGGACGTGGAGAGGATCATCCAGGAGTGGCAGAGCCGAAACGAGAGGTACCAAGCAGAAGGGTACCGGAGGTGGGGAAGGGAGGAGGAGAAGGAGGAGGAGAGCGACGCTGGCTCCTCGGTGGGGAGGCGGCGGCGCACCCTGAGCGAGAGCAGCGCCTGGGAGAGCGTGAGCAGCCACGACATCTGGGTCCTGAAGCAGCAGCTGGAGCTGAACCGCCCGGACCACGGCAGGAGGCGCCGCGCAGACTCGATGTCCTCGGAGAGCACCTGGGACGCATGGAACGAGAGGCTGCTGGAGATTGAGAAGGAG... |
Task1_train_33212 | This sequence change occurs on Chromosome 1. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GAGCGTGAGCAGCCACGACATCTGGGTCCTGAAGCAGCAGCTGGAGCTGAACCGCCCGGACCACGGCAGGAGGCGCCGCGCAGACTCGATGTCCTCGGAGAGCACCTGGGACGCATGGAACGAGAGGCTGCTGGAGATTGAGAAGGAGGCTTCCCGGAGGTACCACGCCAAGAGCAAGAGAGAGGAGGCGGCAGACAGGAGCTCAGAAGCAGGGAGCAGGGTGCGGGAGGATGATGAGGACAGCGTGGGCTCTGAGGCCAGTTCCTTCTACAACTTCTGCAGCAGGAACAAGGACAAGCTCACTGCCCTGGAAAGATGGA... | GAGCGTGAGCAGCCACGACATCTGGGTCCTGAAGCAGCAGCTGGAGCTGAACCGCCCGGACCACGGCAGGAGGCGCCGCGCAGACTCGATGTCCTCGGAGAGCACCTGGGACGCATGGAACGAGAGGCTGCTGGAGATTGAGAAGGAGGCTTCCCGGAGGTACCACGCCAAGAGCAAGAGAGAGGAGGCGGCAGACAGGAGCTCAGAAGCAGGGAGCAGGGTGCGGGAGGATGATGAGGACAGCGTGGGCTCTGAGGCCAGTTCCTTCTACAACTTCTGCAGCAGGAACAAGGACAAGCTCACTGCCCTGGAAAGATGGA... |
Task1_train_33213 | A genomic change on Chromosome 1 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TTCACCATGTTGGCCAGGTTGGTCTCAAACTCCTGAATTCAGGTCATCCTCCTGCCTCAGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACTGTGCCTGGCCATCACAAAGGTCTTCATCCTCATTGTCTTCACATTGAGTAGGCTGAGGAGAAGGAAGAGGAGGGTTGCTCTTGCCATCTCAGGGGTGGCACAGGTAGAAGAAAATCCATGCATAAGTGGACCCATGCAGTTCAAACTCATGTTGCTCAAGGGTCAACTATAGTTATATATAACCTACTAAATATTGCTATTGATAGCCAAGCCCCTTTAATTGG... | TTCACCATGTTGGCCAGGTTGGTCTCAAACTCCTGAATTCAGGTCATCCTCCTGCCTCAGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACTGTGCCTGGCCATCACAAAGGTCTTCATCCTCATTGTCTTCACATTGAGTAGGCTGAGGAGAAGGAAGAGGAGGGTTGCTCTTGCCATCTCAGGGGTGGCACAGGTAGAAGAAAATCCATGCATAAGTGGACCCATGCAGTTCAAACTCATGTTGCTCAAGGGTCAACTATAGTTATATATAACCTACTAAATATTGCTATTGATAGCCAAGCCCCTTTAATTGG... |
Task1_train_33214 | Here is a variant on Chromosome 1. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TAGCACCTAATGGAAGAGGGCTTGTGACTGAGGTCCCAGGAGCAGTGGTGCAGGTTCCATCCAATGAGAACACGGATGGCCATGGGGGTTAAAGGGCTAGATGAGTTAGGACGGACCCTAGAACTTACCTTACAACGAGGTCCCTTATGTTTGAGTCATCAAAATTCCCTTTGGCAAAAACTGCCTGTAAAGTACTTTGTGGCAACCCTGGTATGGGAGCACCTCCCACACTCGCCCCCTCCCCAGTGAATGGTCAGAGCCAAACAGGAGTCCTTGTGCCCCCTGGAGGCCAGGCTTTGGGGGCTGACTTGGATTATGTG... | TAGCACCTAATGGAAGAGGGCTTGTGACTGAGGTCCCAGGAGCAGTGGTGCAGGTTCCATCCAATGAGAACACGGATGGCCATGGGGGTTAAAGGGCTAGATGAGTTAGGACGGACCCTAGAACTTACCTTACAACGAGGTCCCTTATGTTTGAGTCATCAAAATTCCCTTTGGCAAAAACTGCCTGTAAAGTACTTTGTGGCAACCCTGGTATGGGAGCACCTCCCACACTCGCCCCCTCCCCAGTGAATGGTCAGAGCCAAACAGGAGTCCTTGTGCCCCCTGGAGGCCAGGCTTTGGGGGCTGACTTGGATTATGTG... |
Task1_train_33215 | Chromosome 1 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TCTGGAATATCGGATCCAATAATTCCTGGCTCCCCAGAACCTTCTGACTCTACAGGAAGCAGCCTGTGGAATAGCTCATTTTTGCTACCTTCTCTGAATGAAGACTTAAGTTAGGCAGAACAGAGTAAGAAAGAACCATCACCGCAGGACTTACTGAACAGGTTATTCCAGGTCCTATTTGTCTTTTCCTCAGACTCCGTTTGTTGGAAAACGAGTACCTCATGATGTTCCAGGTTTTTAAGCAATTCTTCACAGTAAAATGGAATCCCACAGCTTCCCTCCCCCAGGTACCTGTAGTGAAAACAAGGCAATCTGTTTAC... | TCTGGAATATCGGATCCAATAATTCCTGGCTCCCCAGAACCTTCTGACTCTACAGGAAGCAGCCTGTGGAATAGCTCATTTTTGCTACCTTCTCTGAATGAAGACTTAAGTTAGGCAGAACAGAGTAAGAAAGAACCATCACCGCAGGACTTACTGAACAGGTTATTCCAGGTCCTATTTGTCTTTTCCTCAGACTCCGTTTGTTGGAAAACGAGTACCTCATGATGTTCCAGGTTTTTAAGCAATTCTTCACAGTAAAATGGAATCCCACAGCTTCCCTCCCCCAGGTACCTGTAGTGAAAACAAGGCAATCTGTTTAC... |
Task1_train_33216 | This mutation on Chromosome 1 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TTCAGCAGGGAAGAAAATGATAATGTGAAAAAAAATGTGTGTGTGTGTGTGTGTTTAATTTGGCTGGTCCTGATTTGTAGCCTTTATAATAAAACCATAACTGTAAGTGTAGCACTTTGCTGAGTTCTGTGAGTCATTTCAGTGAATTACTGAACCTGAGGGCATTAAGGAGATCCCCAGATTTGTAGGTAGTTGGTCAGAAGTGCCGGTGGTCTGGGGATCCCAGAGCTTGCAGCTAGTGTCTGAAGTTTGTAGAGGATTCAACCAATGAAATCCTGCACTAACTCCAGGTGGTTATAACATCAGAATTGCACTGCAGG... | TTCAGCAGGGAAGAAAATGATAATGTGAAAAAAAATGTGTGTGTGTGTGTGTGTTTAATTTGGCTGGTCCTGATTTGTAGCCTTTATAATAAAACCATAACTGTAAGTGTAGCACTTTGCTGAGTTCTGTGAGTCATTTCAGTGAATTACTGAACCTGAGGGCATTAAGGAGATCCCCAGATTTGTAGGTAGTTGGTCAGAAGTGCCGGTGGTCTGGGGATCCCAGAGCTTGCAGCTAGTGTCTGAAGTTTGTAGAGGATTCAACCAATGAAATCCTGCACTAACTCCAGGTGGTTATAACATCAGAATTGCACTGCAGG... |
Task1_train_33217 | A genomic change on Chromosome 1 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GCAGTTCAAAAGACCAAAGAACTGGCCAGGCTTTTGTTCAAATACTAATTTTAAAGTAGCCTGGAATAACAGAGTCTAGAAGGGCATATGATAAAAATCTGTATAACCATTAAGGTTTTGGATATGGTGAACCATCTGTAGTGAAGACAAGAAAGGAGACAATGTAGTTCACTTAAAATTCAATAGAGAGACATGTAGAAATACATACTAGATAATGAAAGGATCCAAACAGTGAAGAAGCAGTCCCTTTATATTTTTGAATTTTTTTTCAAGAGTAAAGTGTGTTATGATAGTCATCTTGATTTGTTTGAAATGATGTT... | GCAGTTCAAAAGACCAAAGAACTGGCCAGGCTTTTGTTCAAATACTAATTTTAAAGTAGCCTGGAATAACAGAGTCTAGAAGGGCATATGATAAAAATCTGTATAACCATTAAGGTTTTGGATATGGTGAACCATCTGTAGTGAAGACAAGAAAGGAGACAATGTAGTTCACTTAAAATTCAATAGAGAGACATGTAGAAATACATACTAGATAATGAAAGGATCCAAACAGTGAAGAAGCAGTCCCTTTATATTTTTGAATTTTTTTTCAAGAGTAAAGTGTGTTATGATAGTCATCTTGATTTGTTTGAAATGATGTT... |
Task1_train_33218 | This sequence change occurs on Chromosome 1. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TACTTGTGAATTTTTTGGTCTACCTTTCTAGTTGTAAAATATAAAAATCCTAAAAGATCATATTGATTAACTTCTTGGTGGAATCACTTATCTTGTTTTGATGATAGGAGCAGTATAGCATCAAGTTCTAGAGGAATTGGGAGCCATTGCAAATCTGAGGGTCAGGAGGAATCTTTCGTCCCACAGAGCTCAGTGCAACCACCAGAAGGAGACAGTGAAACAAGTAAGGTGTTATTTTGCTTTTGTTGTTATAAAATTGCAGCATTGGATGTTTATCTACTTTCCTGTTCCCTTCGATGCTGTATTTTGTTTCTTGTTTT... | TACTTGTGAATTTTTTGGTCTACCTTTCTAGTTGTAAAATATAAAAATCCTAAAAGATCATATTGATTAACTTCTTGGTGGAATCACTTATCTTGTTTTGATGATAGGAGCAGTATAGCATCAAGTTCTAGAGGAATTGGGAGCCATTGCAAATCTGAGGGTCAGGAGGAATCTTTCGTCCCACAGAGCTCAGTGCAACCACCAGAAGGAGACAGTGAAACAAGTAAGGTGTTATTTTGCTTTTGTTGTTATAAAATTGCAGCATTGGATGTTTATCTACTTTCCTGTTCCCTTCGATGCTGTATTTTGTTTCTTGTTTT... |
Task1_train_33219 | A mutation on Chromosome 1 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | AAAATTGAAATATACCTCCTCATGCTTTACCCCTGGCCAACTGCAAATTCCTTCCTTTATGCTCCAGCACTCCCTGAACATATTTGCCATGAATGCTATCCTCTCCCCTGCTGAGCACATAAAATGTGCAAGGAAATAGATTAAAACTAGTTGTAAGCCTTTTCTCTTGGTGTAGAAACAGAGTCATAGACGAGTACTGGGTGAATGAATGAAGTATGGAGTCATAAAGTCAATCCCTCCTCCAAACTCCAGGTAGCACTGATAGCTATCTCTAGTTCTGTTGATGTTTTTTGTTCTTATAGAAAAACAGCAAGAAGACA... | AAAATTGAAATATACCTCCTCATGCTTTACCCCTGGCCAACTGCAAATTCCTTCCTTTATGCTCCAGCACTCCCTGAACATATTTGCCATGAATGCTATCCTCTCCCCTGCTGAGCACATAAAATGTGCAAGGAAATAGATTAAAACTAGTTGTAAGCCTTTTCTCTTGGTGTAGAAACAGAGTCATAGACGAGTACTGGGTGAATGAATGAAGTATGGAGTCATAAAGTCAATCCCTCCTCCAAACTCCAGGTAGCACTGATAGCTATCTCTAGTTCTGTTGATGTTTTTTGTTCTTATAGAAAAACAGCAAGAAGACA... |
Task1_train_33220 | A mutation on Chromosome 1 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CTCAGCTATGTTTCCACCTCCTGTCTAATTAACATAACTCGAGGTTCCCAGAACATTTCTACATGGGAAAAATTTGAAAAAAGTAAATCTGTTACTTGAATAAATAGTCCTATAGTCTAGCAATATAACTTTAAGATTTACATAACAGAATGAAAGTCAGAATTGTATTTTATGGCATTAAATAAATTAACTTTATTTCTGTCTATATCAACATCCAAAGTTTATTAGGAATTTATTTAAAGAATAATAAAAGCAATAGGACCTAACATTTAATGAGTGCTTACTGTGTCAAATACCATTCTAAACAGTTTACATGTATT... | CTCAGCTATGTTTCCACCTCCTGTCTAATTAACATAACTCGAGGTTCCCAGAACATTTCTACATGGGAAAAATTTGAAAAAAGTAAATCTGTTACTTGAATAAATAGTCCTATAGTCTAGCAATATAACTTTAAGATTTACATAACAGAATGAAAGTCAGAATTGTATTTTATGGCATTAAATAAATTAACTTTATTTCTGTCTATATCAACATCCAAAGTTTATTAGGAATTTATTTAAAGAATAATAAAAGCAATAGGACCTAACATTTAATGAGTGCTTACTGTGTCAAATACCATTCTAAACAGTTTACATGTATT... |
Task1_train_33221 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GAGTATAGCAGCCCAACCCAGAAAATATGGGCATAAAAAAGCAAAGCCTTCCCCTGAAACCAACTAAAACATGTTAAAAGCCTTAGTACTTGAAGACCATGCCTTGAGCCAAGTTAGTTATAGGATACAATAAAAGTGTATTTCAGAACAAAGAGTGTGTGACATTCAGAAAAGAGAATCCAAATGAAAACAGAATTATCCATCCTTCACACCAGTTAAAGACTAACATCAGTTCATTAATAAAAAGGCAGTGACAACTATATAAAATCACCTGTATAACTTTTGTAAAAATATACACATACCTACACATTTGTGTATAG... | GAGTATAGCAGCCCAACCCAGAAAATATGGGCATAAAAAAGCAAAGCCTTCCCCTGAAACCAACTAAAACATGTTAAAAGCCTTAGTACTTGAAGACCATGCCTTGAGCCAAGTTAGTTATAGGATACAATAAAAGTGTATTTCAGAACAAAGAGTGTGTGACATTCAGAAAAGAGAATCCAAATGAAAACAGAATTATCCATCCTTCACACCAGTTAAAGACTAACATCAGTTCATTAATAAAAAGGCAGTGACAACTATATAAAATCACCTGTATAACTTTTGTAAAAATATACACATACCTACACATTTGTGTATAG... |
Task1_train_33222 | Consider this mutation on Chromosome 1. Is this a benign change or a disease-causing variant? | Benign | ACGAAGCTGGATCTCATGCTCCATTCCCATCTCTTCCCTACCCCCCATTATTTCATAAGATTTTCTTGCCCCTATTATGCCTTAGTAAATTCTAGATCAAGAGAGATCCTGCCCAATTTCAGAGTAGAGAAGCCCAGGACTAGCTGCGTAATTTGTGGGGCTCATTGAAAAATGGAAATGTCGAATTCCTTCTTAAAAAATAAAGGATTTCAAGAGGGTAACTGCAAAGCATTAAATTTAGCATGCGGTCCTTCTGAGCATGTGACCCTTTGCAACTGAACAGATCACACACATCCAAGAAGCTGGCCCTGTAGAAAACA... | ACGAAGCTGGATCTCATGCTCCATTCCCATCTCTTCCCTACCCCCCATTATTTCATAAGATTTTCTTGCCCCTATTATGCCTTAGTAAATTCTAGATCAAGAGAGATCCTGCCCAATTTCAGAGTAGAGAAGCCCAGGACTAGCTGCGTAATTTGTGGGGCTCATTGAAAAATGGAAATGTCGAATTCCTTCTTAAAAAATAAAGGATTTCAAGAGGGTAACTGCAAAGCATTAAATTTAGCATGCGGTCCTTCTGAGCATGTGACCCTTTGCAACTGAACAGATCACACACATCCAAGAAGCTGGCCCTGTAGAAAACA... |
Task1_train_33223 | A mutation found on Chromosome 1 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GGTCACACATTTAGCCTGTGTGGTGCTGCAAATAGTTCATAAATTAGGTGACATTTTTGTACTCCGTATATACTTTGGGTCTATGGGTTTGCCTAGGCTCTATGCCAGAACCCTGTGTTCTGACCCCTTAGGAAGTATATGCACAAGGAAGAAATGAGAAGGAGTTACAGATTGCCTTTTCCCTGTATTTCTTAGCAGGGACCTCTTCCCATTACCCAATCTTTACCAGGCAGAAGGGGCCAGACCCCTAACTGGTGCTGTTTATTGCCATTTTCCAGCAAGGTCTGGCCGTGAAAGTGAACCACGTGAATGTCTTGGGA... | GGTCACACATTTAGCCTGTGTGGTGCTGCAAATAGTTCATAAATTAGGTGACATTTTTGTACTCCGTATATACTTTGGGTCTATGGGTTTGCCTAGGCTCTATGCCAGAACCCTGTGTTCTGACCCCTTAGGAAGTATATGCACAAGGAAGAAATGAGAAGGAGTTACAGATTGCCTTTTCCCTGTATTTCTTAGCAGGGACCTCTTCCCATTACCCAATCTTTACCAGGCAGAAGGGGCCAGACCCCTAACTGGTGCTGTTTATTGCCATTTTCCAGCAAGGTCTGGCCGTGAAAGTGAACCACGTGAATGTCTTGGGA... |
Task1_train_33224 | A genomic variant on Chromosome 1 is under review. What is the biological outcome — benign or pathogenic? | Benign | GAGGGATTTTTATGGTGATGGTGAACATTCTGTGTCTTGACAGTATCAACATCAGTGTGCTGGTTGTGATATAGTATTATAGATTTGCAAAATGTTACCCCTGGGAGAAACTGGGTAAAGAATACTCAGGATACCCAAAGGATCTCTCCGTATTATTTCTCTTGACTGTATGTGAATCTATTTTATTTTTGTTCCAAAATAAAAAGTTTAATTACAAATTATAAATAAATAAATAAAGCACATTATTTCCATCTAGTTCATTGGCTCAGTCTAGGACTGAAGCATGTCGAATTCTCCCACTGACTCTCACATTTCCCAAG... | GAGGGATTTTTATGGTGATGGTGAACATTCTGTGTCTTGACAGTATCAACATCAGTGTGCTGGTTGTGATATAGTATTATAGATTTGCAAAATGTTACCCCTGGGAGAAACTGGGTAAAGAATACTCAGGATACCCAAAGGATCTCTCCGTATTATTTCTCTTGACTGTATGTGAATCTATTTTATTTTTGTTCCAAAATAAAAAGTTTAATTACAAATTATAAATAAATAAATAAAGCACATTATTTCCATCTAGTTCATTGGCTCAGTCTAGGACTGAAGCATGTCGAATTCTCCCACTGACTCTCACATTTCCCAAG... |
Task1_train_33225 | A sequence alteration has been identified on Chromosome 1. Is it disease-inducing or harmless? | Benign | AAATAAAGCACATTATTTCCATCTAGTTCATTGGCTCAGTCTAGGACTGAAGCATGTCGAATTCTCCCACTGACTCTCACATTTCCCAAGCCTGTGGAAACAAGCCAAACACTCACCCATCAAACCCATAATATTTGCTATATACTGTGAGTCATCAACAGAGAATCTCCTTCTGCCTTTCTTCTGGTCTACCTCCCCTACTAATCCCATCTTTCCAGACTCTGAGCATAACATGCAAACTCACAGAACACAAGGGAGTGGGTAAAGCAACTCCGAATGCCATAAAAGTGGGTTGTGAGCCTTGAATGGAATACAAGATT... | AAATAAAGCACATTATTTCCATCTAGTTCATTGGCTCAGTCTAGGACTGAAGCATGTCGAATTCTCCCACTGACTCTCACATTTCCCAAGCCTGTGGAAACAAGCCAAACACTCACCCATCAAACCCATAATATTTGCTATATACTGTGAGTCATCAACAGAGAATCTCCTTCTGCCTTTCTTCTGGTCTACCTCCCCTACTAATCCCATCTTTCCAGACTCTGAGCATAACATGCAAACTCACAGAACACAAGGGAGTGGGTAAAGCAACTCCGAATGCCATAAAAGTGGGTTGTGAGCCTTGAATGGAATACAAGATT... |
Task1_train_33226 | This variant is present on Chromosome 1. Is the change likely to result in a pathogenic outcome? | Benign | ATAATATTTGCTATATACTGTGAGTCATCAACAGAGAATCTCCTTCTGCCTTTCTTCTGGTCTACCTCCCCTACTAATCCCATCTTTCCAGACTCTGAGCATAACATGCAAACTCACAGAACACAAGGGAGTGGGTAAAGCAACTCCGAATGCCATAAAAGTGGGTTGTGAGCCTTGAATGGAATACAAGATTTTGAAGGTGGTTCCATCCCTATTCACTCTGGACAGGCCCTGCATCTCACTCCCTCGGGGCCTTGCTTAGAAATACTCAGGTAGCTAGTTGTTCTCATGTGGTATTGAGTGCAACATTTAAATAGGAA... | ATAATATTTGCTATATACTGTGAGTCATCAACAGAGAATCTCCTTCTGCCTTTCTTCTGGTCTACCTCCCCTACTAATCCCATCTTTCCAGACTCTGAGCATAACATGCAAACTCACAGAACACAAGGGAGTGGGTAAAGCAACTCCGAATGCCATAAAAGTGGGTTGTGAGCCTTGAATGGAATACAAGATTTTGAAGGTGGTTCCATCCCTATTCACTCTGGACAGGCCCTGCATCTCACTCCCTCGGGGCCTTGCTTAGAAATACTCAGGTAGCTAGTTGTTCTCATGTGGTATTGAGTGCAACATTTAAATAGGAA... |
Task1_train_33227 | A variant found on Chromosome 1 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CATCATAGGGCACATAATCAATTTCAGCATAGTCATCTTCACTGCTCTGGACCTCTTCCTTTGGAATGATCTCAATGTAATCTGTACCATCTTTACTGAGGCCCACTATAACCAGTGGATTAAATTCCTTTGATAGAAAAGTATCATTGAGAGTAGGAGATGAAGGAGATGGCATCTGACCAAGGTCTGGATAAGGAAAAGACTCATTAAATTCTTGAAGAAGCAATGACTGACTAGATTCAGAAGGGTAGAATATCTGATCAAGGTCTGGAGGAGGTGATATCTGGCTGAGATCCGGGAGAAGGGTGGTGTCACTGATG... | CATCATAGGGCACATAATCAATTTCAGCATAGTCATCTTCACTGCTCTGGACCTCTTCCTTTGGAATGATCTCAATGTAATCTGTACCATCTTTACTGAGGCCCACTATAACCAGTGGATTAAATTCCTTTGATAGAAAAGTATCATTGAGAGTAGGAGATGAAGGAGATGGCATCTGACCAAGGTCTGGATAAGGAAAAGACTCATTAAATTCTTGAAGAAGCAATGACTGACTAGATTCAGAAGGGTAGAATATCTGATCAAGGTCTGGAGGAGGTGATATCTGGCTGAGATCCGGGAGAAGGGTGGTGTCACTGATG... |
Task1_train_33228 | This is a variant located on Chromosome 1. Is this mutation a likely cause of disease or not? | Benign | TTTCAGCATAGTCATCTTCACTGCTCTGGACCTCTTCCTTTGGAATGATCTCAATGTAATCTGTACCATCTTTACTGAGGCCCACTATAACCAGTGGATTAAATTCCTTTGATAGAAAAGTATCATTGAGAGTAGGAGATGAAGGAGATGGCATCTGACCAAGGTCTGGATAAGGAAAAGACTCATTAAATTCTTGAAGAAGCAATGACTGACTAGATTCAGAAGGGTAGAATATCTGATCAAGGTCTGGAGGAGGTGATATCTGGCTGAGATCCGGGAGAAGGGTGGTGTCACTGATGTCTGGAGAGAGAGTCACCTGG... | TTTCAGCATAGTCATCTTCACTGCTCTGGACCTCTTCCTTTGGAATGATCTCAATGTAATCTGTACCATCTTTACTGAGGCCCACTATAACCAGTGGATTAAATTCCTTTGATAGAAAAGTATCATTGAGAGTAGGAGATGAAGGAGATGGCATCTGACCAAGGTCTGGATAAGGAAAAGACTCATTAAATTCTTGAAGAAGCAATGACTGACTAGATTCAGAAGGGTAGAATATCTGATCAAGGTCTGGAGGAGGTGATATCTGGCTGAGATCCGGGAGAAGGGTGGTGTCACTGATGTCTGGAGAGAGAGTCACCTGG... |
Task1_train_33229 | This alteration on Chromosome 1 may affect genome function. Does it lead to a disease or is it benign? | Benign | CATTGAGAGTAGGAGATGAAGGAGATGGCATCTGACCAAGGTCTGGATAAGGAAAAGACTCATTAAATTCTTGAAGAAGCAATGACTGACTAGATTCAGAAGGGTAGAATATCTGATCAAGGTCTGGAGGAGGTGATATCTGGCTGAGATCCGGGAGAAGGGTGGTGTCACTGATGTCTGGAGAGAGAGTCACCTGGCTGAGGTCTGGGGAAAGGGACATCTGACCAAAGTTTGGGGAAAGATCTGTCTCACCAAGGTCTGGAGAAAGTGTCATCTGGTCGAGGTCTGGGGTAAGGGGAATTTGACTGAGATCTGCAAAG... | CATTGAGAGTAGGAGATGAAGGAGATGGCATCTGACCAAGGTCTGGATAAGGAAAAGACTCATTAAATTCTTGAAGAAGCAATGACTGACTAGATTCAGAAGGGTAGAATATCTGATCAAGGTCTGGAGGAGGTGATATCTGGCTGAGATCCGGGAGAAGGGTGGTGTCACTGATGTCTGGAGAGAGAGTCACCTGGCTGAGGTCTGGGGAAAGGGACATCTGACCAAAGTTTGGGGAAAGATCTGTCTCACCAAGGTCTGGAGAAAGTGTCATCTGGTCGAGGTCTGGGGTAAGGGGAATTTGACTGAGATCTGCAAAG... |
Task1_train_33230 | This variant is located on Chromosome 1. Evaluate its biological effect and specify any disease association. | Benign | GGAGAATAGCAGAAAAATGTGGCAGCCTCTCAGAAGTTACTAGTTGGATTCAGTAGAAGTGAAAGATTCAAACCTGAGGTGAAAGAAGAGTTGACTTCATCTTCATAAGGCGAGAAGGTCACTCCATGAGGGTAAATGCTATAGGGGCGGCTGGCCATATTTTTGAACACGATCTACAAAGTTAAATCAAATTTATTCTAGGATTTAAGGTTGATCATGACAAATAATATAAGATACTAGCTTTGCATATTCACCTTTTGGATGGTGTGTGTGTATACATGTGTACACACAGTAGGAAAATTAGATCTGTTTATCTGAGC... | GGAGAATAGCAGAAAAATGTGGCAGCCTCTCAGAAGTTACTAGTTGGATTCAGTAGAAGTGAAAGATTCAAACCTGAGGTGAAAGAAGAGTTGACTTCATCTTCATAAGGCGAGAAGGTCACTCCATGAGGGTAAATGCTATAGGGGCGGCTGGCCATATTTTTGAACACGATCTACAAAGTTAAATCAAATTTATTCTAGGATTTAAGGTTGATCATGACAAATAATATAAGATACTAGCTTTGCATATTCACCTTTTGGATGGTGTGTGTGTATACATGTGTACACACAGTAGGAAAATTAGATCTGTTTATCTGAGC... |
Task1_train_33231 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TAAACAGTAAAGGAAGAGGGATAGTGTTGCAAGGTTCATTCACTGTGCAAACAGCCCAGGTAGGGTCCAAAGTCTACAATTCTTACCTCCTCCCTTATTTGAAATGAAACCTGCATGTGACATTTTGATATTTTGAGGTTTCTCCCCCTTCTTCTTTACATTGCTGAACTTCTGATGCAGTCGTCTAGAAGCCTCATAAGTAGGTGAAGTGGTTGTTCACTATGTCACTGTATGATTTTAAGAACATAGGAGAAACTCCTGTTCCCACTACCTCACCCAGAGTCTTGCCAAATTCACTTTGGAAGAAATCTCAGTGCCAC... | TAAACAGTAAAGGAAGAGGGATAGTGTTGCAAGGTTCATTCACTGTGCAAACAGCCCAGGTAGGGTCCAAAGTCTACAATTCTTACCTCCTCCCTTATTTGAAATGAAACCTGCATGTGACATTTTGATATTTTGAGGTTTCTCCCCCTTCTTCTTTACATTGCTGAACTTCTGATGCAGTCGTCTAGAAGCCTCATAAGTAGGTGAAGTGGTTGTTCACTATGTCACTGTATGATTTTAAGAACATAGGAGAAACTCCTGTTCCCACTACCTCACCCAGAGTCTTGCCAAATTCACTTTGGAAGAAATCTCAGTGCCAC... |
Task1_train_33232 | This sequence change occurs on Chromosome 1. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | AGTCTGATGAACACAGTTTCCCTTACAGAGAGTTTTCATCTATTTGGTCTTCTCTGTTTAAATCCTGCATCAACTTTACAAATTTTCAGGAGAAAAAGCAAATCTCTTAGCTTATCACACCAGGTCACCAATACAGGGGCAGCTTCTTCTGCCCCTAACTTCATCTCCTGCCTCCTCCATAATCCCCTTTTGATTCAGATGCACTGAACTGCGAAACATACCATCTTCTCATTGATTTTACACTTTCATGTCTTTCTACATGCCATTTTCTCTGATGGAACTCTATTTCCATTTTCCCCTTGGCTAAATGCCTCTCATTC... | AGTCTGATGAACACAGTTTCCCTTACAGAGAGTTTTCATCTATTTGGTCTTCTCTGTTTAAATCCTGCATCAACTTTACAAATTTTCAGGAGAAAAAGCAAATCTCTTAGCTTATCACACCAGGTCACCAATACAGGGGCAGCTTCTTCTGCCCCTAACTTCATCTCCTGCCTCCTCCATAATCCCCTTTTGATTCAGATGCACTGAACTGCGAAACATACCATCTTCTCATTGATTTTACACTTTCATGTCTTTCTACATGCCATTTTCTCTGATGGAACTCTATTTCCATTTTCCCCTTGGCTAAATGCCTCTCATTC... |
Task1_train_33233 | With a mutation on Chromosome 1, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CTTAATTTATTCCTAAGACTTAAATATAAACTGTAATTTCCAAAAGAATTAGGGTAAGGTCCCAATAAAAGAAATTAAATTGTAGACATAAGAAGCCTATACATGTAAGTTTAGGCAAATAAAATAAACTGTGCATAATTTTTTGGCAAAGATTCAGTTATGTAACAAAAGGCAGTCAGGACAAGCTATGAGGGGAAAAAATAGGGGGCTGAAATATACCTTGCAAACAGATGGAATTTAATTAAGGAAGATCTGCTAGGAGGTTTTTAGAGTTAGGTGGTAAGCAAAGGTCTTCTGAGATAATAAATTAGAAATCTGCA... | CTTAATTTATTCCTAAGACTTAAATATAAACTGTAATTTCCAAAAGAATTAGGGTAAGGTCCCAATAAAAGAAATTAAATTGTAGACATAAGAAGCCTATACATGTAAGTTTAGGCAAATAAAATAAACTGTGCATAATTTTTTGGCAAAGATTCAGTTATGTAACAAAAGGCAGTCAGGACAAGCTATGAGGGGAAAAAATAGGGGGCTGAAATATACCTTGCAAACAGATGGAATTTAATTAAGGAAGATCTGCTAGGAGGTTTTTAGAGTTAGGTGGTAAGCAAAGGTCTTCTGAGATAATAAATTAGAAATCTGCA... |
Task1_train_33234 | Chromosome 1 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TCTTCTAACAGCACATATATGAAAATATTCTCTCGAAGGGTGATATCCAAAGAACCAAGATGCAAAGATGGACACATAGTAGCATCCGACAAATACCTGCTAATGCATTGATAAATCTTGCCTCCAAATATACTATTTACAAAATTTTGGTTCTTAAAATACTGTTAGTCTAAATGTTATTACTACATTTGTGATCAACTGGCATGTCAGTATGTGTTTATTGAAATACTTAATAAGTGTTCAGCATATCTGGACACTGGAAGTTTGAAAGAAGTAGACTGTCATCCTCCTTAAACTACATTTTCAGGGAACTTCAGGGT... | TCTTCTAACAGCACATATATGAAAATATTCTCTCGAAGGGTGATATCCAAAGAACCAAGATGCAAAGATGGACACATAGTAGCATCCGACAAATACCTGCTAATGCATTGATAAATCTTGCCTCCAAATATACTATTTACAAAATTTTGGTTCTTAAAATACTGTTAGTCTAAATGTTATTACTACATTTGTGATCAACTGGCATGTCAGTATGTGTTTATTGAAATACTTAATAAGTGTTCAGCATATCTGGACACTGGAAGTTTGAAAGAAGTAGACTGTCATCCTCCTTAAACTACATTTTCAGGGAACTTCAGGGT... |
Task1_train_33235 | This alteration on Chromosome 1 may affect genome function. Does it lead to a disease or is it benign? | Benign | CTACAGTTGGTGTCATACTGAAACGCTCTCAAGGATGGAGAGCAATCCATGCTTCCGTGGACAGGACTCTCCAGCGGCTCACACGAAATAGCTAAGTGGAAAAGGTATCTTCTAAAGCCAGGTAATGGAAGGGCCGGGTTCTTCCTCAGAAAAAATTCCTAGATGCTATATCTTTCCTGTCCACATTTTCAGTGTGTTCAGAACCCTAAAACCTCCATTTTCCAAAAGAGAGACTGCCTGGAACACCTTCCCATGCCCCTCTTGGCCTGACTCACTCTCACCTGCCCTTCAGGTCTCAGCTTAGACTTCCCTTTCCTTAG... | CTACAGTTGGTGTCATACTGAAACGCTCTCAAGGATGGAGAGCAATCCATGCTTCCGTGGACAGGACTCTCCAGCGGCTCACACGAAATAGCTAAGTGGAAAAGGTATCTTCTAAAGCCAGGTAATGGAAGGGCCGGGTTCTTCCTCAGAAAAAATTCCTAGATGCTATATCTTTCCTGTCCACATTTTCAGTGTGTTCAGAACCCTAAAACCTCCATTTTCCAAAAGAGAGACTGCCTGGAACACCTTCCCATGCCCCTCTTGGCCTGACTCACTCTCACCTGCCCTTCAGGTCTCAGCTTAGACTTCCCTTTCCTTAG... |
Task1_train_33236 | This variant is found on Chromosome 1. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | ATTGCAGAGAATTCATTTTGGCGGAATTATGTAATTGCCTGGGATTGCATCACACACTTTTTCGATGCAGTGTTCCTTCCTTTGCTTCTTTGTCAAAGGCTACCCTCAAAGACTACATGGTGAACCACTCTCTTTAGCCACCTTAGCCGCTGCTCCCAACTCCCTCTCAAGTATAGGACATGGTCCTATACCTCGGATATGTCAGTAGAGCAGAAGCTCTATGCTAGGTACTTTATACATGCTATTTAATTGTATACTTTTTATGTACTTAATCCTCACAAGCACCTTGCAATTCTTAGCTCCATTTCACAGATGAGAAA... | ATTGCAGAGAATTCATTTTGGCGGAATTATGTAATTGCCTGGGATTGCATCACACACTTTTTCGATGCAGTGTTCCTTCCTTTGCTTCTTTGTCAAAGGCTACCCTCAAAGACTACATGGTGAACCACTCTCTTTAGCCACCTTAGCCGCTGCTCCCAACTCCCTCTCAAGTATAGGACATGGTCCTATACCTCGGATATGTCAGTAGAGCAGAAGCTCTATGCTAGGTACTTTATACATGCTATTTAATTGTATACTTTTTATGTACTTAATCCTCACAAGCACCTTGCAATTCTTAGCTCCATTTCACAGATGAGAAA... |
Task1_train_33237 | The following genetic variant occurs on Chromosome 1. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CAACCCTCTCCAGAAACTGTATCTATTTCCCTGTTCTGATTGGTGGTACAATAGGTAAATTTAAGACTTGGAAATCAAAGTTTTCACATTTTAGACCCTGCCATGCCATTTAGTAAACAGTACAACTTTCATGTCTTATTCCTCATCTGTCAAATTTAAGCCATTATTGCTACCTTGCTCTAGAGACTTCAAGGAAGAATGGACTCAAGGAATCAGAAGAATTTTTGTATTTGGAAACTATATGAGATGAGATTAGGGAGAAACATGGGAACTAAGAGAAAATGTTATCTTTTTTCATTGATTTAAAGAGTATCTATTAT... | CAACCCTCTCCAGAAACTGTATCTATTTCCCTGTTCTGATTGGTGGTACAATAGGTAAATTTAAGACTTGGAAATCAAAGTTTTCACATTTTAGACCCTGCCATGCCATTTAGTAAACAGTACAACTTTCATGTCTTATTCCTCATCTGTCAAATTTAAGCCATTATTGCTACCTTGCTCTAGAGACTTCAAGGAAGAATGGACTCAAGGAATCAGAAGAATTTTTGTATTTGGAAACTATATGAGATGAGATTAGGGAGAAACATGGGAACTAAGAGAAAATGTTATCTTTTTTCATTGATTTAAAGAGTATCTATTAT... |
Task1_train_33238 | This is a variant located on Chromosome 1. Is this mutation a likely cause of disease or not? | Benign | GAAGGCTTTTGGTAGCTTCCATCTGATTCAAGGCTTTGGCAGCTGCTGTGGAATACATGAGAACACTAGGTAAAGCACTGTCTTCCAACATGAAGAGAGAAAAATATGTGGAATGTTCAATGGCATGCTTTGTATAAGAATGCAACTTACCTGGCAGGAACAAATTTCTTTGCTGCAAAAGAAAAGACAAACAACCATTAATTCAGACTAAATGACTTTTAAGGATATATTAAATCCAGATACAATATGACTTAATTCATCAAGTGTTGCAAACTCGATGCTTCAGGGCCTCTGTAATAATCAGAGCACAAGCATGGCTC... | GAAGGCTTTTGGTAGCTTCCATCTGATTCAAGGCTTTGGCAGCTGCTGTGGAATACATGAGAACACTAGGTAAAGCACTGTCTTCCAACATGAAGAGAGAAAAATATGTGGAATGTTCAATGGCATGCTTTGTATAAGAATGCAACTTACCTGGCAGGAACAAATTTCTTTGCTGCAAAAGAAAAGACAAACAACCATTAATTCAGACTAAATGACTTTTAAGGATATATTAAATCCAGATACAATATGACTTAATTCATCAAGTGTTGCAAACTCGATGCTTCAGGGCCTCTGTAATAATCAGAGCACAAGCATGGCTC... |
Task1_train_33239 | This variant is found on Chromosome 1. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CAAATGTCACTTCCTTAGAGGGGCTTTTTCAGAGCCTTCAATCTTAGGCAGTTCCCCCAAACGCAGTCTTACACTTGTATCACATTGGCCTGTTCAGTTTTCTAAAAAGCACATTACCATTAAAAGAAATGCTCTTGTTTGCTTTGTATATTTTCCACTTCTACACATTATGTTGCAAAGTTCATAAAGGCAGGATGTTGATTTTCTTCACAGCGTTACCCTCAGCACCTAGAACAGTGCCTGACACATAGTAAGCATTCATTAAAGGGCTAAAAATATTTCATGTTTTAAAAATACTTGGGAGTCTAATTAGACAATAC... | CAAATGTCACTTCCTTAGAGGGGCTTTTTCAGAGCCTTCAATCTTAGGCAGTTCCCCCAAACGCAGTCTTACACTTGTATCACATTGGCCTGTTCAGTTTTCTAAAAAGCACATTACCATTAAAAGAAATGCTCTTGTTTGCTTTGTATATTTTCCACTTCTACACATTATGTTGCAAAGTTCATAAAGGCAGGATGTTGATTTTCTTCACAGCGTTACCCTCAGCACCTAGAACAGTGCCTGACACATAGTAAGCATTCATTAAAGGGCTAAAAATATTTCATGTTTTAAAAATACTTGGGAGTCTAATTAGACAATAC... |
Task1_train_33240 | A sequence alteration has been identified on Chromosome 1. Is it disease-inducing or harmless? | Benign | GGTGTGTGCCAGCTGTCCTGGCTAATTTTTAAATTTTTTCTAGGGATAAGGTCTCACTATGTTGCCCAGGTCTTCCAACTCCTGGGCTCAAGTGATCTTCCCGCCTCGGCCTCCCAAAATGCTGGGATTACAGGCGTGAGCCACTACACCCTGCCCATAACTTGACTATTTTTAATTTGTTGTTTAAATCCTCTAAGTTTCTTCAACCATTTTAATCTTAAAATGACTCCTCGTCTGCTACTTATTTTCTGTTTTTCCATATAATATCTAATTTAGCTATTTAAGTTTCAAGTTCCTTGAGGAACTTTGACTTTGTGTAA... | GGTGTGTGCCAGCTGTCCTGGCTAATTTTTAAATTTTTTCTAGGGATAAGGTCTCACTATGTTGCCCAGGTCTTCCAACTCCTGGGCTCAAGTGATCTTCCCGCCTCGGCCTCCCAAAATGCTGGGATTACAGGCGTGAGCCACTACACCCTGCCCATAACTTGACTATTTTTAATTTGTTGTTTAAATCCTCTAAGTTTCTTCAACCATTTTAATCTTAAAATGACTCCTCGTCTGCTACTTATTTTCTGTTTTTCCATATAATATCTAATTTAGCTATTTAAGTTTCAAGTTCCTTGAGGAACTTTGACTTTGTGTAA... |
Task1_train_33241 | This variant lies on Chromosome 1. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GGGAGCCCTTTGGGACAGGATACTTGTTGTATACCACATACAAACTAAGACACTGGTAGTAGCACTCTGAATTGCTATGATAAACCAAAATGCCTTTACATATTTTTCTAGATGACTGTGTAGGGGTTTTGGGGTGCATCCTCCTACCCTTGTGATCCAATGACTAGAATAAAATTTGCATGTAAGCTTTACTCCAGTCCAAAAGGAAGGTTCTTTATATTTAGAATGGATATTGTGATATTACTTATGTTTTTTTTCCAGCCTTATGCAAAAAGAGCTCGTCAGGAGTTCCCCTGGGAAGAAGAGTACAGGTCAGCGCT... | GGGAGCCCTTTGGGACAGGATACTTGTTGTATACCACATACAAACTAAGACACTGGTAGTAGCACTCTGAATTGCTATGATAAACCAAAATGCCTTTACATATTTTTCTAGATGACTGTGTAGGGGTTTTGGGGTGCATCCTCCTACCCTTGTGATCCAATGACTAGAATAAAATTTGCATGTAAGCTTTACTCCAGTCCAAAAGGAAGGTTCTTTATATTTAGAATGGATATTGTGATATTACTTATGTTTTTTTTCCAGCCTTATGCAAAAAGAGCTCGTCAGGAGTTCCCCTGGGAAGAAGAGTACAGGTCAGCGCT... |
Task1_train_33242 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | AAACACATGGCAGTATATTACCACTTCCCCTTCTCATGCTTGAGGCAGACATCACTAATCAATCATAGATCTCTTTTCTGCTGAGTCTAAATGAAGCCTTATAATTCTTTTTAACATAGCATTAGACAGATATTACCAAGGGAATCAGAGGTGACATCCCTAATGGAGAACTGGCTTTGGATTCAGACCGTTCCTGTTCAAATTCTAATTCTGCCATTAGCTATGAAATATTAGAAATCTGAGTTTTCTCATCTCCAAAATGAGGATAATAATCTATATTGTGGAGTTTTCTTATTATAATTACTATAGCTAAGAGCTTG... | AAACACATGGCAGTATATTACCACTTCCCCTTCTCATGCTTGAGGCAGACATCACTAATCAATCATAGATCTCTTTTCTGCTGAGTCTAAATGAAGCCTTATAATTCTTTTTAACATAGCATTAGACAGATATTACCAAGGGAATCAGAGGTGACATCCCTAATGGAGAACTGGCTTTGGATTCAGACCGTTCCTGTTCAAATTCTAATTCTGCCATTAGCTATGAAATATTAGAAATCTGAGTTTTCTCATCTCCAAAATGAGGATAATAATCTATATTGTGGAGTTTTCTTATTATAATTACTATAGCTAAGAGCTTG... |
Task1_train_33243 | This mutation on Chromosome 1 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GTTGATTCTACCCATCCATGAGCATGGGATATGTTTCCTTTTGTTTGTGTCATCTATGATTTATTTCAGCAGTGTTTTGCAGTTTTTCTTGCAGAGGTCTTTTGACTACTTGGTTAGGTATATTCCTAAGTTGTTGTTGGTTTGTTTTTCTCTTTCCTTTTTTTTTTTTGTTTTTTTTTTTTTTTGCAGCCATTGTAAAAGGGGTTGAGTTCTCGATTTGATTCTCCCCTTGGTCGCTGTTGGTATATAGAAGAGCTACTGATTTGTGTACATTAATCTTGTATCTGGAAACTTTGCTGAATTCTTTTATCAGCTCTAGG... | GTTGATTCTACCCATCCATGAGCATGGGATATGTTTCCTTTTGTTTGTGTCATCTATGATTTATTTCAGCAGTGTTTTGCAGTTTTTCTTGCAGAGGTCTTTTGACTACTTGGTTAGGTATATTCCTAAGTTGTTGTTGGTTTGTTTTTCTCTTTCCTTTTTTTTTTTTGTTTTTTTTTTTTTTTGCAGCCATTGTAAAAGGGGTTGAGTTCTCGATTTGATTCTCCCCTTGGTCGCTGTTGGTATATAGAAGAGCTACTGATTTGTGTACATTAATCTTGTATCTGGAAACTTTGCTGAATTCTTTTATCAGCTCTAGG... |
Task1_train_33244 | Here is a mutation located on Chromosome 1. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TATTAATAGATTTATTTCTGGGCTTTTTATTTCATTCAATTTGTCTATGAGTCTGTTTTTATAGCAGTCCCTACAATTTTAATTACTTTTGTATTATAGCTTGAAATCATAACTGTAAGACCTCCATGTTCTTTCTTAAGATTGTTTTGGCTATTGGAGGTCTAGTTCTCCAGTTTCTTGGAAAAAAAGAATGATACATTCTTAGTGGAATCCCTTTAATTACCACTTTTAAAGGCTAAATTCTCATTCCATAGTGTAAGTTTAGTCATTCTTTAATAAGGCCTGACTTAAGTTGCCCTGCTGGCATTTTTTTGTTTTTT... | TATTAATAGATTTATTTCTGGGCTTTTTATTTCATTCAATTTGTCTATGAGTCTGTTTTTATAGCAGTCCCTACAATTTTAATTACTTTTGTATTATAGCTTGAAATCATAACTGTAAGACCTCCATGTTCTTTCTTAAGATTGTTTTGGCTATTGGAGGTCTAGTTCTCCAGTTTCTTGGAAAAAAAGAATGATACATTCTTAGTGGAATCCCTTTAATTACCACTTTTAAAGGCTAAATTCTCATTCCATAGTGTAAGTTTAGTCATTCTTTAATAAGGCCTGACTTAAGTTGCCCTGCTGGCATTTTTTTGTTTTTT... |
Task1_train_33245 | Consider a variant on Chromosome 1. Determine its clinical classification and disease relevance. | Benign | GTGGCCAACAAGAATATGAAAAAAAGCTCAACCTCATTGATGATTAAAGAAATGCAAATCAAAACCACAATGAGATACCAACTACCACCAGTCAGAATGACTATTCTTAAAAAGTCAAAAAACAACAGATGCTGGCAGGGTTGTGGAGAAAAATAAATGTTTATACACTGTTGGTGGGAGTGTAAATTAGTACAACCATTGTACAAAACAGCATGGTGATTCCTCGAAGACCTAAAAACAGAAATACCATTTGACCCAGCAATTCGATTACTGGATATAATATATCCAGAGGAATATAAATTGTTCTGTCATAAAGACAA... | GTGGCCAACAAGAATATGAAAAAAAGCTCAACCTCATTGATGATTAAAGAAATGCAAATCAAAACCACAATGAGATACCAACTACCACCAGTCAGAATGACTATTCTTAAAAAGTCAAAAAACAACAGATGCTGGCAGGGTTGTGGAGAAAAATAAATGTTTATACACTGTTGGTGGGAGTGTAAATTAGTACAACCATTGTACAAAACAGCATGGTGATTCCTCGAAGACCTAAAAACAGAAATACCATTTGACCCAGCAATTCGATTACTGGATATAATATATCCAGAGGAATATAAATTGTTCTGTCATAAAGACAA... |
Task1_train_33246 | A variant was discovered on Chromosome 1. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | ATTCAGTTACATTAACTGAAGTTTAACACCTATTTATGCATGAAAGATAAAAAAAGAAAATCAAAAGAAAACTCTCGCCAAACTTAGAGCAGAATTGTCTTGAACCAGCAAAACATACGCAAACATTATCTTAATCTTTATCTTAATTTATCTTAAATCTGCACTGTTCAATATAGTAGCCACTAGTCACAAAACTGAGATGTGCTATAAGTATAAAATATACAAAAACTTTCCAACTCTTATTATAAAAAAGGAAAGTAAAATACCTTATTAATAAATTTTAATTACATTTTGAAATGTTAACATATCAGACAGATTGA... | ATTCAGTTACATTAACTGAAGTTTAACACCTATTTATGCATGAAAGATAAAAAAAGAAAATCAAAAGAAAACTCTCGCCAAACTTAGAGCAGAATTGTCTTGAACCAGCAAAACATACGCAAACATTATCTTAATCTTTATCTTAATTTATCTTAAATCTGCACTGTTCAATATAGTAGCCACTAGTCACAAAACTGAGATGTGCTATAAGTATAAAATATACAAAAACTTTCCAACTCTTATTATAAAAAAGGAAAGTAAAATACCTTATTAATAAATTTTAATTACATTTTGAAATGTTAACATATCAGACAGATTGA... |
Task1_train_33247 | An alteration has been detected on Chromosome 1. Is it pathogenic, and if so, what disease is involved? | Benign | CAGTCCTTGAACAATAAATATAAATCATGAGACTGAAGAGGCGACAGAAGCTGTTCTTAGAATTGGAAATGCCACAAGCAGAGGCAAGAAGACAAGAAAATGAGCATTGTATATTTTACTATTGTAGGTTATAGTTTCATCTTGCTGGAATGGAGGTTCTTAATGCTAACAATTTGTATGATGCATTATGGTACTCAAATACCTTCCTGTAAATGGGCTCCTTTGCTTGTGGGAAGAAAGTAGTTTTATAACAGAAAGGATAAATGAGGACCAGAAATGTCAATTGTCTTCTTGAAAGTCATTGAGAAAATTAATGTTTG... | CAGTCCTTGAACAATAAATATAAATCATGAGACTGAAGAGGCGACAGAAGCTGTTCTTAGAATTGGAAATGCCACAAGCAGAGGCAAGAAGACAAGAAAATGAGCATTGTATATTTTACTATTGTAGGTTATAGTTTCATCTTGCTGGAATGGAGGTTCTTAATGCTAACAATTTGTATGATGCATTATGGTACTCAAATACCTTCCTGTAAATGGGCTCCTTTGCTTGTGGGAAGAAAGTAGTTTTATAACAGAAAGGATAAATGAGGACCAGAAATGTCAATTGTCTTCTTGAAAGTCATTGAGAAAATTAATGTTTG... |
Task1_train_33248 | Chromosome 1 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | AGGGGAAGGGTATTCCAGACTGAGGACACAGCCAGGGCATTTACGGGCAGGGCTGGCATGATCAACAAACAACAATGGGGCTTCTCTTCCTTGAGAAAAGAGAATGAGGGGAGAATGCCAGGAGATAAAACCAGAGACATAAAAATTGTTGGATGGCGTGGGCCTTGTAGATCATTGTAAGGACTCTGGCTTTTACTCTGAAAGCAATGGGAAACTACAGCAGGCATCTGAGCAAATGAATTACAAGACCTAAATTAGCATTGCAGAGATTGATCGGCTGCTGTGGTCATCATTCAATGTAAGGGTAGGGCAAGGAAGGA... | AGGGGAAGGGTATTCCAGACTGAGGACACAGCCAGGGCATTTACGGGCAGGGCTGGCATGATCAACAAACAACAATGGGGCTTCTCTTCCTTGAGAAAAGAGAATGAGGGGAGAATGCCAGGAGATAAAACCAGAGACATAAAAATTGTTGGATGGCGTGGGCCTTGTAGATCATTGTAAGGACTCTGGCTTTTACTCTGAAAGCAATGGGAAACTACAGCAGGCATCTGAGCAAATGAATTACAAGACCTAAATTAGCATTGCAGAGATTGATCGGCTGCTGTGGTCATCATTCAATGTAAGGGTAGGGCAAGGAAGGA... |
Task1_train_33249 | This mutation is located on Chromosome 1. Is it associated with a disease or is it a benign polymorphism? | Benign | TTTTGCAGAGATGAAGTCTCACTATGTTGCCCAGTCTGACCTTGAACTCCTAGCAATACCCTACCCTGGCCTCCCAAACTGCTGGGATTACAGGCATGAGCCACTGTGCCTGGCCTTTTTTCATTTTAACTGAGAAATGTGTTCAGCTCTTTTGTTCCTTAGTCATTGATCATCACTTTTGTTATATCTGTTAGTCTTGTCATAGAGTTGCTGCACTTATTACACAGAGAAGGCCTTTTATCACGACCAATTTATTTTAGGAAATTTCAGGGAAAACGTTTTTCTAGAACACCTTATTTGACATTATAAAACAACTCTTC... | TTTTGCAGAGATGAAGTCTCACTATGTTGCCCAGTCTGACCTTGAACTCCTAGCAATACCCTACCCTGGCCTCCCAAACTGCTGGGATTACAGGCATGAGCCACTGTGCCTGGCCTTTTTTCATTTTAACTGAGAAATGTGTTCAGCTCTTTTGTTCCTTAGTCATTGATCATCACTTTTGTTATATCTGTTAGTCTTGTCATAGAGTTGCTGCACTTATTACACAGAGAAGGCCTTTTATCACGACCAATTTATTTTAGGAAATTTCAGGGAAAACGTTTTTCTAGAACACCTTATTTGACATTATAAAACAACTCTTC... |
Task1_train_33250 | This alteration occurs on Chromosome 1. Is it associated with a disease or is it a benign variant? | Benign | GTATAACAGTCTTAGTTTAACTGATTCAAAACTATGGCTGGCTTAGTAAATTTAACGCTAGTGGCCAATAATAACAGAAAAGAGATAAATATTCTTAAGTATGTATTTTGAGCCAGGGATTCTGCTAAGTACTTTATTCACTCTCATTAAAGCCTTGAAACAATTGTTGCATGTTTAAGTTATTAATGAGCCCCATTTTACAGAGGAAAATGAGGAAACTGACCTATGTAACTTGCTCATGGTCACAAGCCATTAAAGGTGGCAGAATTAGGATATCAATCCAGTCGGTGTGACTCCAGAACCCTCCTATTTACTCTATA... | GTATAACAGTCTTAGTTTAACTGATTCAAAACTATGGCTGGCTTAGTAAATTTAACGCTAGTGGCCAATAATAACAGAAAAGAGATAAATATTCTTAAGTATGTATTTTGAGCCAGGGATTCTGCTAAGTACTTTATTCACTCTCATTAAAGCCTTGAAACAATTGTTGCATGTTTAAGTTATTAATGAGCCCCATTTTACAGAGGAAAATGAGGAAACTGACCTATGTAACTTGCTCATGGTCACAAGCCATTAAAGGTGGCAGAATTAGGATATCAATCCAGTCGGTGTGACTCCAGAACCCTCCTATTTACTCTATA... |
Task1_train_33251 | This sequence change occurs on Chromosome 1. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TCACCTGGGGAGCTTCTAAAGCCCTGATGGCCTGGAGACCTACCCCCAAAGATTCAAACACTATGGAGTAGGGTTAGAGCAATGAAAGTTTGCTCAGGTGATTTTAATATACAGTCAGGATTAAGGCCTGCTCATCTAAAGCAATTGTTCTCAAATAGAGTCACCTGGAGGGCTTTTGAAAGCACAAATTGCTAGGCCCCACCCTCCATATTTCTGATTCAATAGGTGCTATGGCTTGAATGTCCTGTCCAAAACTCATATTGAGATTAATCCCCAATGGGGCAGTATGAAGAGGTGGGGCCTTTAAGAGGTGATTGAGT... | TCACCTGGGGAGCTTCTAAAGCCCTGATGGCCTGGAGACCTACCCCCAAAGATTCAAACACTATGGAGTAGGGTTAGAGCAATGAAAGTTTGCTCAGGTGATTTTAATATACAGTCAGGATTAAGGCCTGCTCATCTAAAGCAATTGTTCTCAAATAGAGTCACCTGGAGGGCTTTTGAAAGCACAAATTGCTAGGCCCCACCCTCCATATTTCTGATTCAATAGGTGCTATGGCTTGAATGTCCTGTCCAAAACTCATATTGAGATTAATCCCCAATGGGGCAGTATGAAGAGGTGGGGCCTTTAAGAGGTGATTGAGT... |
Task1_train_33252 | This mutation occurs on Chromosome 1. Does this change lead to a known medical condition, or is it benign? | Benign | CACACACACACACACAAAATAAAGTCTTTTAAGTATGGAAGGAAGATTATTTCCCCTGTTATTCTCCATCCAGGGATATTCAGATGCATATACACTTATACTTGTGTAGTCACTAGGCTATAATCGCACATTTCCAAGGATTATAATCATTCTACCTGCACTATAGAAGAAACTTAGGTGAGTGGAAAACATGAGAGGAGGGAGGGAGGAACTTTCTCTTAAGGAGCAGCAAACCACAACTGTAAACATGGGAAAGACTTGTGGATTTTATCATCAGAGTTAGCCCAAAGACTTTCTCGTGTCTCCATGAAGTTCTCAAG... | CACACACACACACACAAAATAAAGTCTTTTAAGTATGGAAGGAAGATTATTTCCCCTGTTATTCTCCATCCAGGGATATTCAGATGCATATACACTTATACTTGTGTAGTCACTAGGCTATAATCGCACATTTCCAAGGATTATAATCATTCTACCTGCACTATAGAAGAAACTTAGGTGAGTGGAAAACATGAGAGGAGGGAGGGAGGAACTTTCTCTTAAGGAGCAGCAAACCACAACTGTAAACATGGGAAAGACTTGTGGATTTTATCATCAGAGTTAGCCCAAAGACTTTCTCGTGTCTCCATGAAGTTCTCAAG... |
Task1_train_33253 | This is a variant located on Chromosome 1. Is this mutation a likely cause of disease or not? | Benign | TAAGAGACATACAGATCTAGTAAAGTGATTTTGAGAACAATGACAGCAATAGGAACAGATAATCGTATGTAGACCTATGTACAAATTCACCAATCCTCTGTTGTTAAAAGACCAGACTGGAATAAGATCATTTGAAACACACTGATGAAAAATACTACAAAATGATGAACATTTATTTATCCTTCTTGCCTTACTTTACTTTTTAGGTACTTCTCAGTACTAGAACTGGTACCTGGGTTCTTGGGCGCTCTTCAGATTGGGGCTATCCTTATAATATGATGGTTACAAGAAGATGCTGTAGTTTTATTGCACAAGTTCTG... | TAAGAGACATACAGATCTAGTAAAGTGATTTTGAGAACAATGACAGCAATAGGAACAGATAATCGTATGTAGACCTATGTACAAATTCACCAATCCTCTGTTGTTAAAAGACCAGACTGGAATAAGATCATTTGAAACACACTGATGAAAAATACTACAAAATGATGAACATTTATTTATCCTTCTTGCCTTACTTTACTTTTTAGGTACTTCTCAGTACTAGAACTGGTACCTGGGTTCTTGGGCGCTCTTCAGATTGGGGCTATCCTTATAATATGATGGTTACAAGAAGATGCTGTAGTTTTATTGCACAAGTTCTG... |
Task1_train_33254 | A variant on Chromosome 1 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | AATCTATAGGAATCCAAGTGAATAGTCAGTTTCAGCAAGAATTTCCCAGCCTGCAGGCAGCTGGGGATCAGGAAAAAAAAGAAAAGGAAACAAATGATGACAACTATGGACCTGGACCCAGTTTACGTCCACCAAGTAAGAGTACTTTCTCTTTAATACAAAATGAGATCATATTTGTGTATTATCTTGCAATACAACCTCCTGCTTGCTGTTGCATATATTATTTGCCTACTTCGAAAAGGCAGACTTTGTACTATAGTCACTTGCTACTCAGGTATGATTTTTGCACCGACAGTATCACTGTAACTTGAGAACATGTT... | AATCTATAGGAATCCAAGTGAATAGTCAGTTTCAGCAAGAATTTCCCAGCCTGCAGGCAGCTGGGGATCAGGAAAAAAAAGAAAAGGAAACAAATGATGACAACTATGGACCTGGACCCAGTTTACGTCCACCAAGTAAGAGTACTTTCTCTTTAATACAAAATGAGATCATATTTGTGTATTATCTTGCAATACAACCTCCTGCTTGCTGTTGCATATATTATTTGCCTACTTCGAAAAGGCAGACTTTGTACTATAGTCACTTGCTACTCAGGTATGATTTTTGCACCGACAGTATCACTGTAACTTGAGAACATGTT... |
Task1_train_33255 | This variant is present on Chromosome 1. Is the change likely to result in a pathogenic outcome? | Benign | TAATCTTTGTATTTTTTATAGAGATGGGGTTTTGCCGTGTTGCCCAGGCTGGTCTTGAACTCTTGGGCTCAAGCAGTCTGACTGCCTTACCTCCCAAAGTGCTGGGATTATAGACGTGAGCCATCGTGTGCAGCCACTTGGGATGTCTTTATTGTAGAGTAGGTGTGAAGAAATTTAGGTGTATCTACAATGCTTATATAATATAGCTAGATGTAATTTTTCCATTAGTGAGATGTTTCTTTTTAACAGTATTTTAGGGAACATTTTTAAGGCCAAGATAAGGAGAAATACAATAATACAAAGTTAACTTTGAAATGGCG... | TAATCTTTGTATTTTTTATAGAGATGGGGTTTTGCCGTGTTGCCCAGGCTGGTCTTGAACTCTTGGGCTCAAGCAGTCTGACTGCCTTACCTCCCAAAGTGCTGGGATTATAGACGTGAGCCATCGTGTGCAGCCACTTGGGATGTCTTTATTGTAGAGTAGGTGTGAAGAAATTTAGGTGTATCTACAATGCTTATATAATATAGCTAGATGTAATTTTTCCATTAGTGAGATGTTTCTTTTTAACAGTATTTTAGGGAACATTTTTAAGGCCAAGATAAGGAGAAATACAATAATACAAAGTTAACTTTGAAATGGCG... |
Task1_train_33256 | This genomic variant is located on Chromosome 1. Can you determine its pathogenicity and name any linked disease? | Benign | TACCTGGTATATAGTAAGTAATCATTATTATGTGTGCCCTGCTTTTAGAGCAATTGCCAGGTTTGCAGCCTGAGCTGATAAGAATTTAAGAATTTATTTGGACTGTATGGTATTAATCTGAGTTCCTTAGTTTTACATACTTAGCACTTCAGATTACTATACCCATAAGGTATATTTGTCTATTTTCTGTTGATATAACTAAATACCTGAGATCTGGTAATTTATAAAGAAAAGAAATGTATTTCTTGCAAATCTGTTGGCTGCAAAGTCGAAGGTTGAGGGGGCGACATCTCATGAGGGCCTTCTTGTTGGTAGAGACT... | TACCTGGTATATAGTAAGTAATCATTATTATGTGTGCCCTGCTTTTAGAGCAATTGCCAGGTTTGCAGCCTGAGCTGATAAGAATTTAAGAATTTATTTGGACTGTATGGTATTAATCTGAGTTCCTTAGTTTTACATACTTAGCACTTCAGATTACTATACCCATAAGGTATATTTGTCTATTTTCTGTTGATATAACTAAATACCTGAGATCTGGTAATTTATAAAGAAAAGAAATGTATTTCTTGCAAATCTGTTGGCTGCAAAGTCGAAGGTTGAGGGGGCGACATCTCATGAGGGCCTTCTTGTTGGTAGAGACT... |
Task1_train_33257 | Assess the clinical impact of this variant found on Chromosome 1. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GATTCAAGTCTCAAGCTCTACCACTGACCAGCTGGGCAACCTTGGCCCCTTAGCATCTTAGGACTTCACTTTCCTTGGTTGTAAAATTCAGAATTGGATCTCTTCTAATTCTAACAATCTAAACATTTTTTAAAAATCCTTTACATCTTATAGGTATTTCATGTGAACCCCACAAAAATTATTCACAGCAGGAATTTTCTTTGTTATGTTATGGACAAGAAATGAAGATGCAGAGGGTTCAATAACTTGCCCAAGGTCATCCCCAGGCTCTGGCTCTTAGGTTTTCTAACCCCATAGCTATGAAGAGCTTGCCTTTCACG... | GATTCAAGTCTCAAGCTCTACCACTGACCAGCTGGGCAACCTTGGCCCCTTAGCATCTTAGGACTTCACTTTCCTTGGTTGTAAAATTCAGAATTGGATCTCTTCTAATTCTAACAATCTAAACATTTTTTAAAAATCCTTTACATCTTATAGGTATTTCATGTGAACCCCACAAAAATTATTCACAGCAGGAATTTTCTTTGTTATGTTATGGACAAGAAATGAAGATGCAGAGGGTTCAATAACTTGCCCAAGGTCATCCCCAGGCTCTGGCTCTTAGGTTTTCTAACCCCATAGCTATGAAGAGCTTGCCTTTCACG... |
Task1_train_33258 | Chromosome 1 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CCGTGGAAAGAATTCCCACTGCAGTGTCCCGGAGCCTGCGTGTGGTGGGCAAGCTCCTCAAATGGTATCTCACAGGGAATAGGGGAGTCTTGAAAACGCAGCTTCGGCAGTAGGAACATGAACCTCTTACCTAAAAGTTCCAGGGAGTTTGGCTCCGTTGACTATTGGGAGAAGTTCTTCCAGCAGCGAGGAAAGAAAGCTTTCGAGTGGTATGGAACCTACCTGGAACTGTGCGGGGTGCTACATAAATATATCAAGCCCAGGGAAAAGGTGAGGAGCGCGGGTTGGTAGCCCTTCGTACGTGCTCCGGAAGGTGGGAA... | CCGTGGAAAGAATTCCCACTGCAGTGTCCCGGAGCCTGCGTGTGGTGGGCAAGCTCCTCAAATGGTATCTCACAGGGAATAGGGGAGTCTTGAAAACGCAGCTTCGGCAGTAGGAACATGAACCTCTTACCTAAAAGTTCCAGGGAGTTTGGCTCCGTTGACTATTGGGAGAAGTTCTTCCAGCAGCGAGGAAAGAAAGCTTTCGAGTGGTATGGAACCTACCTGGAACTGTGCGGGGTGCTACATAAATATATCAAGCCCAGGGAAAAGGTGAGGAGCGCGGGTTGGTAGCCCTTCGTACGTGCTCCGGAAGGTGGGAA... |
Task1_train_33259 | Chromosome 1 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TGCTTTCAAGCTTACTATGACAGATACAAGTTTTGCAAAATTCGAATTTTTACTTACAGGCTGTAATTTTAGGATTGGAATCCAATACTATCAGCTGTTTTCCTTGACATGTTATACAACTGAATTAAGGTTTCATGGGACAGTAACCACAGCTTGTGATACATTTGAATTACTGTAGTTTGTCAGTGATTCTTTCAAGTAAATATAGTGTTTTTTGAAAAAAGCACAACTCAAACAATCACACAAGTGTTTTTCCTTGAAACAAGCATTGAACTGCAGGAAGCAGAAGAAATGTTTTATGTCTACTTCCTCTTTTCTTT... | TGCTTTCAAGCTTACTATGACAGATACAAGTTTTGCAAAATTCGAATTTTTACTTACAGGCTGTAATTTTAGGATTGGAATCCAATACTATCAGCTGTTTTCCTTGACATGTTATACAACTGAATTAAGGTTTCATGGGACAGTAACCACAGCTTGTGATACATTTGAATTACTGTAGTTTGTCAGTGATTCTTTCAAGTAAATATAGTGTTTTTTGAAAAAAGCACAACTCAAACAATCACACAAGTGTTTTTCCTTGAAACAAGCATTGAACTGCAGGAAGCAGAAGAAATGTTTTATGTCTACTTCCTCTTTTCTTT... |
Task1_train_33260 | A change on Chromosome 1 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | ACTACAATTTCATAGAACTCTTTACTATCTTCAACCACCAACACCTAGCCCTGTTCCTGATGTGGACTATAGAATAATTATGAGGCATGCCTCTATTGAGGCACAAGCCCAAACCAGGAGCAGGCAGTGGACAGATGCTTTGGGCTTCAGAGGTTAGTCCCTGAAACCCTTTTCTCCTCATTGGCCAGTGTCCTTGGATATAGAAAGCAGTCCAATTGACCTTACAGAAAACCACCAATTTTTTTTATCACAAAACACAATATTCATCTGTCCAAATAAAACTCTGATAAAGAATGTGACATGACAAGAGCTGAAGACAC... | ACTACAATTTCATAGAACTCTTTACTATCTTCAACCACCAACACCTAGCCCTGTTCCTGATGTGGACTATAGAATAATTATGAGGCATGCCTCTATTGAGGCACAAGCCCAAACCAGGAGCAGGCAGTGGACAGATGCTTTGGGCTTCAGAGGTTAGTCCCTGAAACCCTTTTCTCCTCATTGGCCAGTGTCCTTGGATATAGAAAGCAGTCCAATTGACCTTACAGAAAACCACCAATTTTTTTTATCACAAAACACAATATTCATCTGTCCAAATAAAACTCTGATAAAGAATGTGACATGACAAGAGCTGAAGACAC... |
Task1_train_33261 | Mutation context: Chromosome 1. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | ATATACTAAAAACTACTAAATTGCACATTAAGATGGTGACTTATGATACATGATATCATAAACACCGATAAAAAGAAATTAGCACTAAATAAAAGCACAAAATAGATGAATCTCAAAAAAATGTAAATAGGACCTGGTTATGTAACTACTCATATTCCTATGTAACCTTGGGCTAGAAGCTCAATCATTCAGTGCAGAAGAAATACCTGCTGACAGTTATGGTTGTGAATCACCAGTGATATTTGCCTTGGTTTTATCTAGGCTGTGTTTCATCATGTCTCTGCTCCAAACAGCTCATCTTCCCCTTAATGCACCTATTC... | ATATACTAAAAACTACTAAATTGCACATTAAGATGGTGACTTATGATACATGATATCATAAACACCGATAAAAAGAAATTAGCACTAAATAAAAGCACAAAATAGATGAATCTCAAAAAAATGTAAATAGGACCTGGTTATGTAACTACTCATATTCCTATGTAACCTTGGGCTAGAAGCTCAATCATTCAGTGCAGAAGAAATACCTGCTGACAGTTATGGTTGTGAATCACCAGTGATATTTGCCTTGGTTTTATCTAGGCTGTGTTTCATCATGTCTCTGCTCCAAACAGCTCATCTTCCCCTTAATGCACCTATTC... |
Task1_train_33262 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TGGAGGGCTTTCTTGTGCACCGTAGGATGTGAAACAGCATCCCTGGCCTCTACTCACTAGATGCCAGTAGTACTTCTCCAATGTGACAAGCAAAAAATGTGTTCACACAATGCCAATCTCACCCTGGGGGGAAGTCTGCCCCAGGTTGAGAATTACTGTATTATAGTTAAGGGGTGGTTGATAGTGGTTACTTAGCCTAAGCCTTAAAAGATTATATATATAATTAAATATTATATATGAAAGATTATACATTATACATGCTCTTTTTCTATATTCTTTCTTGCCATTTTTGGCATATGTTATACTTTTAAGTATGGTGA... | TGGAGGGCTTTCTTGTGCACCGTAGGATGTGAAACAGCATCCCTGGCCTCTACTCACTAGATGCCAGTAGTACTTCTCCAATGTGACAAGCAAAAAATGTGTTCACACAATGCCAATCTCACCCTGGGGGGAAGTCTGCCCCAGGTTGAGAATTACTGTATTATAGTTAAGGGGTGGTTGATAGTGGTTACTTAGCCTAAGCCTTAAAAGATTATATATATAATTAAATATTATATATGAAAGATTATACATTATACATGCTCTTTTTCTATATTCTTTCTTGCCATTTTTGGCATATGTTATACTTTTAAGTATGGTGA... |
Task1_train_33263 | Located on Chromosome 1, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TGGAAAAAGCTCGGAGTAGTGAAGGATTAAACCTTAACATGAAACCATGGAAATGAAGCTGCAAAAAGAGAAAAGAACATTTATAGATTGAAATAGTAAAAGCTAATAATTGGATGATAATTAGGTGAATGGAAAGCCTACCACGGGGGTATTAATAAAGCTCCAACTGCAGGAGAAGGAAGGAAGGAAGGGAGGAAGGCAGGCAGGCAGTCAAGGAAGGAATGAAAGAGAAAGAAAAAAGTAAAATTATTTGTACTTGCATGTTTCAAAAAATCATTGCAGGGACTTGGTGGAAAATAAGTGGATGGGTTTGTGAGTTT... | TGGAAAAAGCTCGGAGTAGTGAAGGATTAAACCTTAACATGAAACCATGGAAATGAAGCTGCAAAAAGAGAAAAGAACATTTATAGATTGAAATAGTAAAAGCTAATAATTGGATGATAATTAGGTGAATGGAAAGCCTACCACGGGGGTATTAATAAAGCTCCAACTGCAGGAGAAGGAAGGAAGGAAGGGAGGAAGGCAGGCAGGCAGTCAAGGAAGGAATGAAAGAGAAAGAAAAAAGTAAAATTATTTGTACTTGCATGTTTCAAAAAATCATTGCAGGGACTTGGTGGAAAATAAGTGGATGGGTTTGTGAGTTT... |
Task1_train_33264 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GTTTCATTGGAGGTGCTTAATCTCAGACAAGACCATCAGAAATCAGTTTGTATTACCTGAACTTTATCAGGGAGAAACATTTCTAACCCAAAGCAACCACCTAGAAAACAAGATTATCAGACTAGCTCAACAAAGGAACACGAAGAGAGTATAGATTTATTTTTCTCCAGTGGCATCTTCTGCAGTGAAGAACATCCTTAAATACCTAATAATGTTTGTATATCTGAACTACTGAATAAGAAAAAATAATGCAAAAGAGAGAAGTGTGGAACAAGAATAAAGTGAAAGAAAAATGGAAATATTTTAACTATATGGGGAAA... | GTTTCATTGGAGGTGCTTAATCTCAGACAAGACCATCAGAAATCAGTTTGTATTACCTGAACTTTATCAGGGAGAAACATTTCTAACCCAAAGCAACCACCTAGAAAACAAGATTATCAGACTAGCTCAACAAAGGAACACGAAGAGAGTATAGATTTATTTTTCTCCAGTGGCATCTTCTGCAGTGAAGAACATCCTTAAATACCTAATAATGTTTGTATATCTGAACTACTGAATAAGAAAAAATAATGCAAAAGAGAGAAGTGTGGAACAAGAATAAAGTGAAAGAAAAATGGAAATATTTTAACTATATGGGGAAA... |
Task1_train_33265 | Here is a variant on Chromosome 1. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TTTTTGGGTTCTTGGAAAAGGGTGAGTCTGTTTTACATGTCGGAGGGGTAGAAATATTGTGGCCAGTGGGCAAACTGTGGAACAGTAAATATGGCCACAAATTCTGTGCATGTCTTACTATTAAGAGGTTGAATCTATTGCCCCACCCCTTGAATTGAGGCAGCCTCATTCACAAGTCTGGAAGTTAGGTACTGGCCCTTTTGCCTCAGTTTTCCTCTAGGTGGCTTCTCATTCTTCAGAGACTGCTTCTTTGCATGGCAGTCTCAGGGTGGCATTCGGAGTGGGAAAAAGGTAGAAGCTACAAATCTTCTCAATGCCTA... | TTTTTGGGTTCTTGGAAAAGGGTGAGTCTGTTTTACATGTCGGAGGGGTAGAAATATTGTGGCCAGTGGGCAAACTGTGGAACAGTAAATATGGCCACAAATTCTGTGCATGTCTTACTATTAAGAGGTTGAATCTATTGCCCCACCCCTTGAATTGAGGCAGCCTCATTCACAAGTCTGGAAGTTAGGTACTGGCCCTTTTGCCTCAGTTTTCCTCTAGGTGGCTTCTCATTCTTCAGAGACTGCTTCTTTGCATGGCAGTCTCAGGGTGGCATTCGGAGTGGGAAAAAGGTAGAAGCTACAAATCTTCTCAATGCCTA... |
Task1_train_33266 | This alteration on Chromosome 1 may affect genome function. Does it lead to a disease or is it benign? | Benign | GATATAAATAGCTATTGAGCACTAGAAATGTGGCTAGGGTGACTAAGGAACTACATTTTAAATTTTATTTAATTTTAAATAATTCAAATTTGAATAGTCACATGTGGCTAGTATCTATTATATTGGACAGTGCAGCTCTAACATTAGTGGAATATGAGCACAATAAAACTCACCATCGAGAGTCATGAAGCCTGGTACCATTCTACACTTTCTCCCTAATTCTTTATTTTTGTTAAGCCCTGTGACTAAAAGAAGTACTTGCAAAGACCAGAAAAGAATGGGTGGATGGTATGAGTTGCATGCAACTCAAAAGACAATGC... | GATATAAATAGCTATTGAGCACTAGAAATGTGGCTAGGGTGACTAAGGAACTACATTTTAAATTTTATTTAATTTTAAATAATTCAAATTTGAATAGTCACATGTGGCTAGTATCTATTATATTGGACAGTGCAGCTCTAACATTAGTGGAATATGAGCACAATAAAACTCACCATCGAGAGTCATGAAGCCTGGTACCATTCTACACTTTCTCCCTAATTCTTTATTTTTGTTAAGCCCTGTGACTAAAAGAAGTACTTGCAAAGACCAGAAAAGAATGGGTGGATGGTATGAGTTGCATGCAACTCAAAAGACAATGC... |
Task1_train_33267 | A mutation located on Chromosome 1 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CCTTTTTTTCATTATGTTGAAATGACTTTTTTTTTTTTTTTTTTTTGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAATGGCCCAGTCTCAGCTCACTGCATCCTCTACCTTCCAGGCTCAAATGATTCTCATGCCTCAGCCTCCTGAGTAGCTAGGATTACAGGTGCACAGAACTGGCACAGCTACTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAAGCTGGTGTTGAACTCCTGAGGTGATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGTATAAGCCACCGTGCCAAGCCTACT... | CCTTTTTTTCATTATGTTGAAATGACTTTTTTTTTTTTTTTTTTTTGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAATGGCCCAGTCTCAGCTCACTGCATCCTCTACCTTCCAGGCTCAAATGATTCTCATGCCTCAGCCTCCTGAGTAGCTAGGATTACAGGTGCACAGAACTGGCACAGCTACTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAAGCTGGTGTTGAACTCCTGAGGTGATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGTATAAGCCACCGTGCCAAGCCTACT... |
Task1_train_33268 | A mutation has occurred on Chromosome 1. What is the medical relevance of this mutation? | Benign | TAGGATTTCTGTATAGTTGTTAAAAGTTAAAACTGTTAATTTGGCATTGAGAAGGCACTTTAGGGTAATCATTGGTTAATGGGTATAAATGTGGCATTCGGAAGTTTTTGAATGTGTTAGACTGTGTGTGCTTGTACAAGAAAAAGTGGCAGAATATGTGAATAAAACAAAGGAAAACAGAAGACCTCATACTTTAACAGACTCTTCTGTTATAGGGAGTATTCCTGTTTCAAGCAAGTTACAAATATTGTATTCCTAGACTAATACAGTTCAAGAAGTACTTTGAATTCACTTTATCTAAAGTGAGGGATTTATTAATG... | TAGGATTTCTGTATAGTTGTTAAAAGTTAAAACTGTTAATTTGGCATTGAGAAGGCACTTTAGGGTAATCATTGGTTAATGGGTATAAATGTGGCATTCGGAAGTTTTTGAATGTGTTAGACTGTGTGTGCTTGTACAAGAAAAAGTGGCAGAATATGTGAATAAAACAAAGGAAAACAGAAGACCTCATACTTTAACAGACTCTTCTGTTATAGGGAGTATTCCTGTTTCAAGCAAGTTACAAATATTGTATTCCTAGACTAATACAGTTCAAGAAGTACTTTGAATTCACTTTATCTAAAGTGAGGGATTTATTAATG... |
Task1_train_33269 | A genomic change on Chromosome 1 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TTTTTTGAGAACTGAATGACATAGTACATTTTGAATGCTTAATGTATTGCTTTGTGCATGGTATTATTTAATAAATATTAGCTTTGGTTATACTTGCAATGTTCTGTTATTTCTCTTTTTCACACATGTTGCTTGCAATCTATATGGCATCTATTTTAGCATTAAAGTAGAAAGTTTTAAGTAGAAAGGTTCTGTCATAAAGAAAAAAAGAATCTTAAGAAGATAAATCTAAGTGGAAATTTAAAGAAAATAAGGCTTTTTTAGATCTAGCCTGTAAACTCCTTTAGACTCTTGAATTTGATATTCTGGTAGCTCTTCCG... | TTTTTTGAGAACTGAATGACATAGTACATTTTGAATGCTTAATGTATTGCTTTGTGCATGGTATTATTTAATAAATATTAGCTTTGGTTATACTTGCAATGTTCTGTTATTTCTCTTTTTCACACATGTTGCTTGCAATCTATATGGCATCTATTTTAGCATTAAAGTAGAAAGTTTTAAGTAGAAAGGTTCTGTCATAAAGAAAAAAAGAATCTTAAGAAGATAAATCTAAGTGGAAATTTAAAGAAAATAAGGCTTTTTTAGATCTAGCCTGTAAACTCCTTTAGACTCTTGAATTTGATATTCTGGTAGCTCTTCCG... |
Task1_train_33270 | A mutation on Chromosome 1 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | AAATCCCAGTTCTACCACTTTTTAGCTGTGTGACTTTGGGTAAATCCCTTATGTTTCCTCAACTGTCCAACAGGGATGATTCTATCAGCTAGTATAGTTCTGAGAACTAGAGATGATGTGTAGAAGATTCCTGGCCCTTAGAGGAATTTACAAATCAGTAAATTATAATTATTTTATTAGTAAAAATTACAATTATAATTGTAAAATAATTACAATTTAATTTTACAAATAATGAAGGTTCTCCCCCAACGCAACCCCGTCACTTTTAAACATAAACTGCCCAGGCTGATCCAATGATAATGAACAGTACTTTGGCATAG... | AAATCCCAGTTCTACCACTTTTTAGCTGTGTGACTTTGGGTAAATCCCTTATGTTTCCTCAACTGTCCAACAGGGATGATTCTATCAGCTAGTATAGTTCTGAGAACTAGAGATGATGTGTAGAAGATTCCTGGCCCTTAGAGGAATTTACAAATCAGTAAATTATAATTATTTTATTAGTAAAAATTACAATTATAATTGTAAAATAATTACAATTTAATTTTACAAATAATGAAGGTTCTCCCCCAACGCAACCCCGTCACTTTTAAACATAAACTGCCCAGGCTGATCCAATGATAATGAACAGTACTTTGGCATAG... |
Task1_train_33271 | This mutation on Chromosome 1 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GAACCCAGTGCTTCTGACTTTGGATTTAGTTCTCATACCACTCTCCTGTGCTGCCTTGTTGAAAATCCAAGAATCCAGCTGTGGGGATAAGGTCTATATCCATGAAACAACTGAAAACCAGCATATGATATGGAGAAACCATAAGAACAGGAAACTGCCTTACCACAAGTAAAATGCCCAGATCTCACTCTTTGGTACCAGTTCATAGTGTTCATTGATCAGCAATTTTTTTTTTCAGACATTGACAGCCCCCAAAACCTGGTGACCGACCGGGTGACAGAGAATATGGCCACTGTCTCCTGGGACCCGGTGCGGGCCAC... | GAACCCAGTGCTTCTGACTTTGGATTTAGTTCTCATACCACTCTCCTGTGCTGCCTTGTTGAAAATCCAAGAATCCAGCTGTGGGGATAAGGTCTATATCCATGAAACAACTGAAAACCAGCATATGATATGGAGAAACCATAAGAACAGGAAACTGCCTTACCACAAGTAAAATGCCCAGATCTCACTCTTTGGTACCAGTTCATAGTGTTCATTGATCAGCAATTTTTTTTTTCAGACATTGACAGCCCCCAAAACCTGGTGACCGACCGGGTGACAGAGAATATGGCCACTGTCTCCTGGGACCCGGTGCGGGCCAC... |
Task1_train_33272 | Here is a mutation located on Chromosome 1. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CTAGAAGAGTGATATGATGCAGTGTTCATTTAAAAAACATTTTCCAGGCCACAGTGAGGAGAATAAATGGAGAAAATGACAAGGATAGAAGTTGGGAGGTTCGTAGGGAAGCTGCTAGAAAAGTCTGGGTGCAAAATGCTGCTTGTCTAGGTAAGCATGATGGCAAAAGGGACAGAGAAGAGGGGATGTCTGGAATATATTTTTGAGGTATGGATGATAATACCTGTTGATAGATGTGGGGTAGGAAGAAAATGAGGACTCAAGTATGACCTGTGTTTTTTATTTGAGCAACATGGGAGATTGGACTACCATTTCTTGAG... | CTAGAAGAGTGATATGATGCAGTGTTCATTTAAAAAACATTTTCCAGGCCACAGTGAGGAGAATAAATGGAGAAAATGACAAGGATAGAAGTTGGGAGGTTCGTAGGGAAGCTGCTAGAAAAGTCTGGGTGCAAAATGCTGCTTGTCTAGGTAAGCATGATGGCAAAAGGGACAGAGAAGAGGGGATGTCTGGAATATATTTTTGAGGTATGGATGATAATACCTGTTGATAGATGTGGGGTAGGAAGAAAATGAGGACTCAAGTATGACCTGTGTTTTTTATTTGAGCAACATGGGAGATTGGACTACCATTTCTTGAG... |
Task1_train_33273 | A mutation on Chromosome 1 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | AAAACATTTTCCAGGCCACAGTGAGGAGAATAAATGGAGAAAATGACAAGGATAGAAGTTGGGAGGTTCGTAGGGAAGCTGCTAGAAAAGTCTGGGTGCAAAATGCTGCTTGTCTAGGTAAGCATGATGGCAAAAGGGACAGAGAAGAGGGGATGTCTGGAATATATTTTTGAGGTATGGATGATAATACCTGTTGATAGATGTGGGGTAGGAAGAAAATGAGGACTCAAGTATGACCTGTGTTTTTTATTTGAGCAACATGGGAGATTGGACTACCATTTCTTGAGAGGGGAGACTGAGAAATAAAAAGTTTGGGGAGA... | AAAACATTTTCCAGGCCACAGTGAGGAGAATAAATGGAGAAAATGACAAGGATAGAAGTTGGGAGGTTCGTAGGGAAGCTGCTAGAAAAGTCTGGGTGCAAAATGCTGCTTGTCTAGGTAAGCATGATGGCAAAAGGGACAGAGAAGAGGGGATGTCTGGAATATATTTTTGAGGTATGGATGATAATACCTGTTGATAGATGTGGGGTAGGAAGAAAATGAGGACTCAAGTATGACCTGTGTTTTTTATTTGAGCAACATGGGAGATTGGACTACCATTTCTTGAGAGGGGAGACTGAGAAATAAAAAGTTTGGGGAGA... |
Task1_train_33274 | This variant lies on Chromosome 1. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CTCCCCAGCCATCCATTCTAGGGGGACTGAGAGGTGGAGACAGGAAGGGCAGCTTGTCCTGGTGAGCAGTGGCAGTTGTGGGGAGATGTCTTCCACATCCCTGGGTTTGGTGCAGGCAGATGGCAAGTCATTCTGTTATGTGAAGGGCACAGCCAGAGGCCCCATGACAAACTCTCTATGTGACAAGGGGATAGAGAACCAGAGTGCTTCTTTCTCTGGTCAAAGGGGTTGATGAGTGGGAGGCCTGAGTGCTTAGGCAGTTTATGGCCATATAGGGTGAGAGGGCAAATGTGACTGGCTATAAAATATATGCAGGTTTA... | CTCCCCAGCCATCCATTCTAGGGGGACTGAGAGGTGGAGACAGGAAGGGCAGCTTGTCCTGGTGAGCAGTGGCAGTTGTGGGGAGATGTCTTCCACATCCCTGGGTTTGGTGCAGGCAGATGGCAAGTCATTCTGTTATGTGAAGGGCACAGCCAGAGGCCCCATGACAAACTCTCTATGTGACAAGGGGATAGAGAACCAGAGTGCTTCTTTCTCTGGTCAAAGGGGTTGATGAGTGGGAGGCCTGAGTGCTTAGGCAGTTTATGGCCATATAGGGTGAGAGGGCAAATGTGACTGGCTATAAAATATATGCAGGTTTA... |
Task1_train_33275 | This variant is found on Chromosome 1. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CTATCCTTTCTCTGCTTAATTCACCCCCGTTAATCTGCTTGGTCAGCATATCTTCTCATCTCCTTGCTGTGCCTTTAGGAGTGCGTCTGTCTGGAAAAGGCATTTATTATATTTACTTTAACTGGCTGTGTTTGGCAAGGTGGTCTGGGATTTCAACTTGGGAGGAAAACTGCTTTGATTATACTGCCCTTGTTTACCGTATGCACTCTTTGCTGTGTATCCCTTGTCTATCAAGACAGCAAATACTTTTGCAGGAATCCAAGACACAAATTAAACAAAATCTCTGTCTGTGAGCACATTGGCAGCTCCTGGTCCATGAC... | CTATCCTTTCTCTGCTTAATTCACCCCCGTTAATCTGCTTGGTCAGCATATCTTCTCATCTCCTTGCTGTGCCTTTAGGAGTGCGTCTGTCTGGAAAAGGCATTTATTATATTTACTTTAACTGGCTGTGTTTGGCAAGGTGGTCTGGGATTTCAACTTGGGAGGAAAACTGCTTTGATTATACTGCCCTTGTTTACCGTATGCACTCTTTGCTGTGTATCCCTTGTCTATCAAGACAGCAAATACTTTTGCAGGAATCCAAGACACAAATTAAACAAAATCTCTGTCTGTGAGCACATTGGCAGCTCCTGGTCCATGAC... |
Task1_train_33276 | A mutation on Chromosome 1 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GTGTTACAAACCTGTCTCGCTCCCTCCCTGCCTGCCATCTGACTCACTCTGCTCATTCATCAAAACCCAGCTCCATGGTTACTTCAAAGGCTCCCCAGGACCTCACTCTCATTTAGTTACTGTTTGCTATGACCCCTCTGGGATTCTACGCATGTCTCTGTCCTAGACCTTACTGTGGGATAACTACAGTGGTTAATTTATCTGCCTAGCATGATTCAAGTAAACGTATTAAACAAATACAAATGGAGTACCTGCTGGCATCCTTCTTTGCACTTGGCCTTGAGGATATGAAGTCTAGTAAGTTACATCCTTGTTTAATT... | GTGTTACAAACCTGTCTCGCTCCCTCCCTGCCTGCCATCTGACTCACTCTGCTCATTCATCAAAACCCAGCTCCATGGTTACTTCAAAGGCTCCCCAGGACCTCACTCTCATTTAGTTACTGTTTGCTATGACCCCTCTGGGATTCTACGCATGTCTCTGTCCTAGACCTTACTGTGGGATAACTACAGTGGTTAATTTATCTGCCTAGCATGATTCAAGTAAACGTATTAAACAAATACAAATGGAGTACCTGCTGGCATCCTTCTTTGCACTTGGCCTTGAGGATATGAAGTCTAGTAAGTTACATCCTTGTTTAATT... |
Task1_train_33277 | This variant is present on Chromosome 1. Is the change likely to result in a pathogenic outcome? | Benign | AGAGATTATTTAGTCCGACAGGAGGACAATGAGACCAACAAAGGTCAGAAAATGGACCCAATGATATGCCAGAGGTAGAAATAAAAACACACATTGAATTATATTCTAATGTTATGATTTGGCACTCCTCTACTCTTAGCTTCTTCACTCGTCATCTCCATTCTTTAGGAAAGGGCAAAATTAGAAAGAAAAACAGAACAGCGGATGGCAAAGACAAAATATGTCTAAGGAAGAAACATGTGACAGTGACTGAACTCCAGCTAGGGCCACTTGTCTTTGTGTTTAGAAATTAAAGAGTTCAAAAGATGGCCAGATGGAAA... | AGAGATTATTTAGTCCGACAGGAGGACAATGAGACCAACAAAGGTCAGAAAATGGACCCAATGATATGCCAGAGGTAGAAATAAAAACACACATTGAATTATATTCTAATGTTATGATTTGGCACTCCTCTACTCTTAGCTTCTTCACTCGTCATCTCCATTCTTTAGGAAAGGGCAAAATTAGAAAGAAAAACAGAACAGCGGATGGCAAAGACAAAATATGTCTAAGGAAGAAACATGTGACAGTGACTGAACTCCAGCTAGGGCCACTTGTCTTTGTGTTTAGAAATTAAAGAGTTCAAAAGATGGCCAGATGGAAA... |
Task1_train_33278 | This mutation on Chromosome 1 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | AGACCAACAAAGGTCAGAAAATGGACCCAATGATATGCCAGAGGTAGAAATAAAAACACACATTGAATTATATTCTAATGTTATGATTTGGCACTCCTCTACTCTTAGCTTCTTCACTCGTCATCTCCATTCTTTAGGAAAGGGCAAAATTAGAAAGAAAAACAGAACAGCGGATGGCAAAGACAAAATATGTCTAAGGAAGAAACATGTGACAGTGACTGAACTCCAGCTAGGGCCACTTGTCTTTGTGTTTAGAAATTAAAGAGTTCAAAAGATGGCCAGATGGAAAGCATTTCTCAACCCATCTCTTAAAACTGGTG... | AGACCAACAAAGGTCAGAAAATGGACCCAATGATATGCCAGAGGTAGAAATAAAAACACACATTGAATTATATTCTAATGTTATGATTTGGCACTCCTCTACTCTTAGCTTCTTCACTCGTCATCTCCATTCTTTAGGAAAGGGCAAAATTAGAAAGAAAAACAGAACAGCGGATGGCAAAGACAAAATATGTCTAAGGAAGAAACATGTGACAGTGACTGAACTCCAGCTAGGGCCACTTGTCTTTGTGTTTAGAAATTAAAGAGTTCAAAAGATGGCCAGATGGAAAGCATTTCTCAACCCATCTCTTAAAACTGGTG... |
Task1_train_33279 | This mutation is located on Chromosome 1. Is it associated with a disease or is it a benign polymorphism? | Benign | TAAACAAAGATAAACATAATTAAGGGCACAGACCTTGTTTGTCTTTTTTGCTACTGCTTCCACAGTGCCTAGAGCAATGCTTGCACATAAGGTTCGCTATAAATATCTGTTGAATCAATGAAGTGCATAGAATGGTTCTAGATGACATCCAATACAATTCAGTTGTTGTTTGTTGCTGTTAAAGCTAATATCAGTTACCTTGAGACCTAGATTCAAGAGAACTGGTTTTGCATCCTTGCCTGGTTTGACAAGCTTTATGACCTTGGATTAGCCGTGCAGCTTCTCAAGGTCTCGAGTTTCCTCATCTGAAAAAGAGGGAG... | TAAACAAAGATAAACATAATTAAGGGCACAGACCTTGTTTGTCTTTTTTGCTACTGCTTCCACAGTGCCTAGAGCAATGCTTGCACATAAGGTTCGCTATAAATATCTGTTGAATCAATGAAGTGCATAGAATGGTTCTAGATGACATCCAATACAATTCAGTTGTTGTTTGTTGCTGTTAAAGCTAATATCAGTTACCTTGAGACCTAGATTCAAGAGAACTGGTTTTGCATCCTTGCCTGGTTTGACAAGCTTTATGACCTTGGATTAGCCGTGCAGCTTCTCAAGGTCTCGAGTTTCCTCATCTGAAAAAGAGGGAG... |
Task1_train_33280 | A genomic change on Chromosome 1 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | AAAATGCGGTATACGTATACGATGGAATACACTCAGCCATTAAAATGAACAAAATAATGTCTTTTGCAGCAACTTGGATGAAGCCGGAGTCCATTATTCTAAGTGAAGTACACAGGAGTGGAAAACCGAAAACCATATGTTCTCACTTATAAGTGGGGAGCTATGAGTATGTGAAGACACACAGAGTGACATAATGGACTTTAGAGATTCAGAAGAGGAAGGGTGGGAGGAGGGTCAGGGATAAAAAAAACTACATATTAGGTACAACCCACATCCACGCCAACACTACTTGGCTGGTGGGTGCACTAAAATGTCAGAAT... | AAAATGCGGTATACGTATACGATGGAATACACTCAGCCATTAAAATGAACAAAATAATGTCTTTTGCAGCAACTTGGATGAAGCCGGAGTCCATTATTCTAAGTGAAGTACACAGGAGTGGAAAACCGAAAACCATATGTTCTCACTTATAAGTGGGGAGCTATGAGTATGTGAAGACACACAGAGTGACATAATGGACTTTAGAGATTCAGAAGAGGAAGGGTGGGAGGAGGGTCAGGGATAAAAAAAACTACATATTAGGTACAACCCACATCCACGCCAACACTACTTGGCTGGTGGGTGCACTAAAATGTCAGAAT... |
Task1_train_33281 | Consider this mutation on Chromosome 1. Is this a benign change or a disease-causing variant? | Benign | TCTATTAACCAAAAACCACTTGTGCCCCAAAAGCTACTGAAATGTTTTCAAAGAGAACCATATCAGAAGGGTTTCTTAATAGAACTCAGGGAATCTCAAGCAAGCAAACATGGTTCAAGTGGAAACAACCAACCCCTGGGTCTGGAGTGGCAATACTGACAAGAAGAAAAAGCCTCAATAAATTATATTGATACCATCATAAAAAGTAATATAGCCTTCAAAAGGCCTAAAACTCTACAAGAGTTATCTAACCAGACTTAAAGAAATAAAAATGTTTTCCTAGCAATAGATATGAAATCCATACTGATGTGGACAACTCA... | TCTATTAACCAAAAACCACTTGTGCCCCAAAAGCTACTGAAATGTTTTCAAAGAGAACCATATCAGAAGGGTTTCTTAATAGAACTCAGGGAATCTCAAGCAAGCAAACATGGTTCAAGTGGAAACAACCAACCCCTGGGTCTGGAGTGGCAATACTGACAAGAAGAAAAAGCCTCAATAAATTATATTGATACCATCATAAAAAGTAATATAGCCTTCAAAAGGCCTAAAACTCTACAAGAGTTATCTAACCAGACTTAAAGAAATAAAAATGTTTTCCTAGCAATAGATATGAAATCCATACTGATGTGGACAACTCA... |
Task1_train_33282 | Chromosome 1 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | AAAAGCTACTGAAATGTTTTCAAAGAGAACCATATCAGAAGGGTTTCTTAATAGAACTCAGGGAATCTCAAGCAAGCAAACATGGTTCAAGTGGAAACAACCAACCCCTGGGTCTGGAGTGGCAATACTGACAAGAAGAAAAAGCCTCAATAAATTATATTGATACCATCATAAAAAGTAATATAGCCTTCAAAAGGCCTAAAACTCTACAAGAGTTATCTAACCAGACTTAAAGAAATAAAAATGTTTTCCTAGCAATAGATATGAAATCCATACTGATGTGGACAACTCATCAAGAATTTGTCACAGCCCTGGCCAAG... | AAAAGCTACTGAAATGTTTTCAAAGAGAACCATATCAGAAGGGTTTCTTAATAGAACTCAGGGAATCTCAAGCAAGCAAACATGGTTCAAGTGGAAACAACCAACCCCTGGGTCTGGAGTGGCAATACTGACAAGAAGAAAAAGCCTCAATAAATTATATTGATACCATCATAAAAAGTAATATAGCCTTCAAAAGGCCTAAAACTCTACAAGAGTTATCTAACCAGACTTAAAGAAATAAAAATGTTTTCCTAGCAATAGATATGAAATCCATACTGATGTGGACAACTCATCAAGAATTTGTCACAGCCCTGGCCAAG... |
Task1_train_33283 | A change on Chromosome 1 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CCTAACTCCCCATCTCCCCTTCCCCCAGGCCCTGGTCACTGCCATTCCACTTTATGTCTCTGAATTTGCCTATTCTATGTATCTCACGTAGGTGGAGTCATATGACATATTGCCCTCTTCTGTTATATTTACATTTTTTACTCTCAATAGAGCACAATTGATACAAACCTTTGGAAATACTTTAGGAAAATAAAGAAAAAAACTTTATTTTTTATTCAAATGAATATAGTGTTGACTTTGTGCCGGGCACTGTTTTAAGGGCTTTATATGTAGTGATTCATTTAATCCTTACAATAGTCCTGTGAGCTAGGTGCTATTAT... | CCTAACTCCCCATCTCCCCTTCCCCCAGGCCCTGGTCACTGCCATTCCACTTTATGTCTCTGAATTTGCCTATTCTATGTATCTCACGTAGGTGGAGTCATATGACATATTGCCCTCTTCTGTTATATTTACATTTTTTACTCTCAATAGAGCACAATTGATACAAACCTTTGGAAATACTTTAGGAAAATAAAGAAAAAAACTTTATTTTTTATTCAAATGAATATAGTGTTGACTTTGTGCCGGGCACTGTTTTAAGGGCTTTATATGTAGTGATTCATTTAATCCTTACAATAGTCCTGTGAGCTAGGTGCTATTAT... |
Task1_train_33284 | A variant found on Chromosome 1 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CACAGTGATTGTAACATCCTCATTGCTGTTTACAGAATTTTGTTTGTTTGTTTTTTTCTTCACTAGTGTACCCTAAAAATAAAATCCTAAGCTCCTCCATTGACTTAACAGACTCCCTTTTGGCCAAGGGGACCCCAGAAAAACCTTAAAAACTGAGTTCCCAGCCATGACAGGATGGGAGGTGAGACACCCCTCATTATACCCCCTCTCTTTTGCAGTTTAGACACAACTGACCAGCATTAATGTTAAAACAGAGATCTTAAGACTAACAGAAAAGACTCTTGGTGGCCATAAGATACCAAACTATACACAGAACCTAA... | CACAGTGATTGTAACATCCTCATTGCTGTTTACAGAATTTTGTTTGTTTGTTTTTTTCTTCACTAGTGTACCCTAAAAATAAAATCCTAAGCTCCTCCATTGACTTAACAGACTCCCTTTTGGCCAAGGGGACCCCAGAAAAACCTTAAAAACTGAGTTCCCAGCCATGACAGGATGGGAGGTGAGACACCCCTCATTATACCCCCTCTCTTTTGCAGTTTAGACACAACTGACCAGCATTAATGTTAAAACAGAGATCTTAAGACTAACAGAAAAGACTCTTGGTGGCCATAAGATACCAAACTATACACAGAACCTAA... |
Task1_train_33285 | With a mutation on Chromosome 1, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CCGGGGCGGCAGGCAGGACGTTCAAACATCAGCAGTGAGGCAGGAGCCTCCAGCAGAGAGGCCTCTGCAAGGTTTTGCCTTCATATTATAAAATACAGACCTTTAGGGGACATAAAAAGAAATCCTACACCCTCCCACGCTTAAGCTAATGAGGAAAAGTTCAGTAGATAACTTAGCCCCAGGTACTAAGTGCCAAAAAGCAAAGCTGCAAATACAGCTGCCTGCAGCTGCCTGACAGTGACGGTGGTGGCCTCATCTGGGCTCAGTTACCTGGAAAGAAGGGATGAAGGATTTGGGGCGGCCCAGCATCTGACAGTACT... | CCGGGGCGGCAGGCAGGACGTTCAAACATCAGCAGTGAGGCAGGAGCCTCCAGCAGAGAGGCCTCTGCAAGGTTTTGCCTTCATATTATAAAATACAGACCTTTAGGGGACATAAAAAGAAATCCTACACCCTCCCACGCTTAAGCTAATGAGGAAAAGTTCAGTAGATAACTTAGCCCCAGGTACTAAGTGCCAAAAAGCAAAGCTGCAAATACAGCTGCCTGCAGCTGCCTGACAGTGACGGTGGTGGCCTCATCTGGGCTCAGTTACCTGGAAAGAAGGGATGAAGGATTTGGGGCGGCCCAGCATCTGACAGTACT... |
Task1_train_33286 | This mutation on Chromosome 1 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | AGCCTGCACCTGCTCTCCCACCAGAACAGAACTTACCCCATTCTGGCGACAAAGGAGAACCAAGAGCTGCCACAGTAGAGCTGAGTCTCTGCTCCCCAGTGTCTCAGATTTGCAGCTCTGAGCTGCTTTCTGCTGGCAAAACGTCATAATATCCACCTTATGTACATCTTCCCTACATGGAAAAAATTTAGGGAGCAAAGAGTGAGCAGGCAGACACTTCCCTGTTTCGGACCCCAGGCTCCTCCTAAGTGTGCAAGTGCTGGCTGGGCTGTGATTGAGATAGAAATCTGACAAGCCAGGGCTAAGGTAATGAGTCTATA... | AGCCTGCACCTGCTCTCCCACCAGAACAGAACTTACCCCATTCTGGCGACAAAGGAGAACCAAGAGCTGCCACAGTAGAGCTGAGTCTCTGCTCCCCAGTGTCTCAGATTTGCAGCTCTGAGCTGCTTTCTGCTGGCAAAACGTCATAATATCCACCTTATGTACATCTTCCCTACATGGAAAAAATTTAGGGAGCAAAGAGTGAGCAGGCAGACACTTCCCTGTTTCGGACCCCAGGCTCCTCCTAAGTGTGCAAGTGCTGGCTGGGCTGTGATTGAGATAGAAATCTGACAAGCCAGGGCTAAGGTAATGAGTCTATA... |
Task1_train_33287 | A variant on Chromosome 1 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GGCCTGGGTCTCTGACAGCCCAGCCTTCATCACCCTTGGGGATAGAATTTTGGTCTGACATGGGCCCTTGTCCCTGGTCCTTGAGTATTAGATTTGATCAAAACAACAGTTTTATAGGTAGACTAAATACCAGGATGGAAGAATGGATGAGATAGTATAGCAGCAGGTGGGGGAAACATTAGGGAAAGCAGAGCTTAAGAGTTCTTGTAGCTATATGGCCTCACAAGTTCAGTTTAAGTCCTAATTTCTTCATCTATACAATGGGAAAATAATAGTACCTAAGGTCAGGATTACATGAAATCACATATGCAAATGGTTTA... | GGCCTGGGTCTCTGACAGCCCAGCCTTCATCACCCTTGGGGATAGAATTTTGGTCTGACATGGGCCCTTGTCCCTGGTCCTTGAGTATTAGATTTGATCAAAACAACAGTTTTATAGGTAGACTAAATACCAGGATGGAAGAATGGATGAGATAGTATAGCAGCAGGTGGGGGAAACATTAGGGAAAGCAGAGCTTAAGAGTTCTTGTAGCTATATGGCCTCACAAGTTCAGTTTAAGTCCTAATTTCTTCATCTATACAATGGGAAAATAATAGTACCTAAGGTCAGGATTACATGAAATCACATATGCAAATGGTTTA... |
Task1_train_33288 | A mutation on Chromosome 1 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GGGGGTGGAGATCCTGCTGGCTGGTCTTGGTGGAGAGATCCAAGGCAAAACAAGCCAAATTCCCAGAAAAGGGAATGGGGAGCAGGTATGTACCTGGCTTTGGAGAGGTGGTCAGGCTGAGAGAGGGCTTCGTGGAGATGAGGTGCCCGACGTCAGGGTCTGTAAAACAGAAACAGACCACGAGTTATGGGGAGGCCCAGGATCCTCTGCAGGCAGGAGCTGTCCGGTTATAGCCGGGAAAACCTAGCTCAGGGGCAGACAGGCTGGTCCATCCCTTTCCACATCGATTCAATCCATTCAATAAATACTGGGCACCTATT... | GGGGGTGGAGATCCTGCTGGCTGGTCTTGGTGGAGAGATCCAAGGCAAAACAAGCCAAATTCCCAGAAAAGGGAATGGGGAGCAGGTATGTACCTGGCTTTGGAGAGGTGGTCAGGCTGAGAGAGGGCTTCGTGGAGATGAGGTGCCCGACGTCAGGGTCTGTAAAACAGAAACAGACCACGAGTTATGGGGAGGCCCAGGATCCTCTGCAGGCAGGAGCTGTCCGGTTATAGCCGGGAAAACCTAGCTCAGGGGCAGACAGGCTGGTCCATCCCTTTCCACATCGATTCAATCCATTCAATAAATACTGGGCACCTATT... |
Task1_train_33289 | A variant was discovered on Chromosome 1. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | ACCAGTGTCAGGGCTGGGAAATCACCACCTAGGAAATGCATCAGAAGTGCTGCAGGTGGCTCCAGAAGTTCCAGTGGCCTCCAGGAAGGATAGTCCCAAGCAGGTGTGTGAAATGGGAGGGTAAGTGTGGTCAGTAGTGGCCTGCATGGGGATGTCATTCACATGCAATTTGCATTAGTTCCTGTACTCCTGTGCTGTCTGTCCTCAGATGTCCATGTTGGCCTTTTCTGTGCAACTAGCAGTTGAAATGAGAGGGAAGAAGGAAGTGAATGACCAGTGATAAGAGGAAAAGAGAAATCAATTTCACCAACCCAGATCCC... | ACCAGTGTCAGGGCTGGGAAATCACCACCTAGGAAATGCATCAGAAGTGCTGCAGGTGGCTCCAGAAGTTCCAGTGGCCTCCAGGAAGGATAGTCCCAAGCAGGTGTGTGAAATGGGAGGGTAAGTGTGGTCAGTAGTGGCCTGCATGGGGATGTCATTCACATGCAATTTGCATTAGTTCCTGTACTCCTGTGCTGTCTGTCCTCAGATGTCCATGTTGGCCTTTTCTGTGCAACTAGCAGTTGAAATGAGAGGGAAGAAGGAAGTGAATGACCAGTGATAAGAGGAAAAGAGAAATCAATTTCACCAACCCAGATCCC... |
Task1_train_33290 | A mutation on Chromosome 1 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TTGTACTAACATTTAAAAATGCTTTTCAAGAAGGTATTTTATGAAATCATCTCTATGCAGATGGTGTAATTTCTTGATCAATTTTCTATAGTACATCAATTAAACTGTTACCAAATCTTTCATTTTTAATGAAAATTATTTTATTGGAATAAATTGTTTTTATTTCTGTTTTATGACAACCCAAACCTGTTTTTCTCTGTGACAAATATTGTCAGTTATAGCTTCTACCATCTTAGAATTTTTCTCATGTCCACTATTTCCATTCAATTTACCCAGGTCACATTTTATAGATCAAAACTTTGTCAAGATTTTATTATTCC... | TTGTACTAACATTTAAAAATGCTTTTCAAGAAGGTATTTTATGAAATCATCTCTATGCAGATGGTGTAATTTCTTGATCAATTTTCTATAGTACATCAATTAAACTGTTACCAAATCTTTCATTTTTAATGAAAATTATTTTATTGGAATAAATTGTTTTTATTTCTGTTTTATGACAACCCAAACCTGTTTTTCTCTGTGACAAATATTGTCAGTTATAGCTTCTACCATCTTAGAATTTTTCTCATGTCCACTATTTCCATTCAATTTACCCAGGTCACATTTTATAGATCAAAACTTTGTCAAGATTTTATTATTCC... |
Task1_train_33291 | This alteration occurs on Chromosome 1. Is it associated with a disease or is it a benign variant? | Benign | GCCTCCTGTGTAGACCACCCAGAGCCTCCTCCATGGCTGGGTAGATACAAAAATAAAACTGGCCACGTATTGAGTGTTGATGATGTGCTCATTGAATGAGCTCATTTAATCTTCACAGCAGCCCTATGAGGGGACTATTTTATTATCCCTTTTTATAGGTGAGGAAACAGGCATGGGACGGTTCAGTAACATCCATGGTTGCACAAATAGAAAATGGTAATCACTATATTAGACTGCCATTCAGACTCAAACGACATTTGTTGAGTGAGTTAATTTTTTTTCTTTTCTCTTTTTTCTTTTTTTTTTTTTTTTGAGATGGA... | GCCTCCTGTGTAGACCACCCAGAGCCTCCTCCATGGCTGGGTAGATACAAAAATAAAACTGGCCACGTATTGAGTGTTGATGATGTGCTCATTGAATGAGCTCATTTAATCTTCACAGCAGCCCTATGAGGGGACTATTTTATTATCCCTTTTTATAGGTGAGGAAACAGGCATGGGACGGTTCAGTAACATCCATGGTTGCACAAATAGAAAATGGTAATCACTATATTAGACTGCCATTCAGACTCAAACGACATTTGTTGAGTGAGTTAATTTTTTTTCTTTTCTCTTTTTTCTTTTTTTTTTTTTTTTGAGATGGA... |
Task1_train_33292 | Mutation context: Chromosome 1. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | AAACCCTGACTGGGTGTGGTGGCGGGTGCCTGTAATCCCAACTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAACTGAGATCAGACTGCTGCACTCCAACTTGGGTGACAAAGCAAGACTCTGTCTCAAAAAAAAAAAAAAAAAAAAAATTAAGTATTGGCTGGGCATAGTGGCACACAACTGTAGTCCCAGCTACCCAGGAAGCTGAGGTAGGATTGTCTGAGCCTGGGAGGTTGAGCCTGCAGTGAGCCAAGATCACACCATTGTACTCCAATCTAGACAATAGAACAAAA... | AAACCCTGACTGGGTGTGGTGGCGGGTGCCTGTAATCCCAACTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAACTGAGATCAGACTGCTGCACTCCAACTTGGGTGACAAAGCAAGACTCTGTCTCAAAAAAAAAAAAAAAAAAAAAATTAAGTATTGGCTGGGCATAGTGGCACACAACTGTAGTCCCAGCTACCCAGGAAGCTGAGGTAGGATTGTCTGAGCCTGGGAGGTTGAGCCTGCAGTGAGCCAAGATCACACCATTGTACTCCAATCTAGACAATAGAACAAAA... |
Task1_train_33293 | Given a variant located on Chromosome 1, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CGGGGTTTCACCATGTTGGTCAGGCTGGTCTCAAACTTTTGACCTCGTGATCTGCCCACCTCAACCTCCCAAAGTGCTGGGATTACAGGCATAAGCCACTGCGCCCGGCCCATTACAACTCTTCATCAAATATTTCCAGCTGCCCTCCCAGGCACATAACAAAACTACACTTTCTCCATGCCCCCCGGCATTACATGAGACCACATGACTTGCTTTGGCCAGTGAGATATAAAAGGAAGTGACATATATCCCTTCTGGCTTTTAGTTTCCACTAGTACTTGACTCATTACTCTGTTTCTCTCTGCAATGCTAACTGCCAG... | CGGGGTTTCACCATGTTGGTCAGGCTGGTCTCAAACTTTTGACCTCGTGATCTGCCCACCTCAACCTCCCAAAGTGCTGGGATTACAGGCATAAGCCACTGCGCCCGGCCCATTACAACTCTTCATCAAATATTTCCAGCTGCCCTCCCAGGCACATAACAAAACTACACTTTCTCCATGCCCCCCGGCATTACATGAGACCACATGACTTGCTTTGGCCAGTGAGATATAAAAGGAAGTGACATATATCCCTTCTGGCTTTTAGTTTCCACTAGTACTTGACTCATTACTCTGTTTCTCTCTGCAATGCTAACTGCCAG... |
Task1_train_33294 | This sequence change occurs on Chromosome 1. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | TCGGCTCACTGCAACCTCCTCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCACCACCACGCCCAGCTAATTTTCTATTTTTAGTAGAGATGGTGTTTCTCCATGTTGGTCAGGCTCATCTTGAACTCCCGACCTTAGGTGATCCGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAAGCATGAGCCACCGTGCCCGGGTGAGAAACACTTTTCTGTGAGAAACACTTTTGTGTGGATTTTGTATCTCTCCAATCAGTGACACCTGGCTTTGAGACATTCTTTAGAGC... | TCGGCTCACTGCAACCTCCTCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCACCACCACGCCCAGCTAATTTTCTATTTTTAGTAGAGATGGTGTTTCTCCATGTTGGTCAGGCTCATCTTGAACTCCCGACCTTAGGTGATCCGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAAGCATGAGCCACCGTGCCCGGGTGAGAAACACTTTTCTGTGAGAAACACTTTTGTGTGGATTTTGTATCTCTCCAATCAGTGACACCTGGCTTTGAGACATTCTTTAGAGC... |
Task1_train_33295 | Here is a genetic alteration on Chromosome 1. Based on the data, is it a benign variant or a cause of disease? | Benign | CCTCTGGTGCACAAGGGCCCTGAGCTTTACACAGCGCTCCATATGTATTAGGTAAAAGAGATAGCGAGAAAGGGGGGCGGTGATTGTCGAGTAATTGTCAATGGGCCATTTGGTTCACAGCAGGCTTGTGAGACTGCATCCTTTGAACAATAGGTGCTAGATTTCTCAATAGATAACTTCAAGGAGCCCAGCGCCAAGGAGTGATGTCCCTCAGCAAACCTTTTGGTGGCAGGCGCAGTGTGAGTTTGTTCACATCTTGCATTCATGATAAACAGTTTGCTGTTTGATCATATAGCCTCAAGTGGAGCGCTGAGTTGGTC... | CCTCTGGTGCACAAGGGCCCTGAGCTTTACACAGCGCTCCATATGTATTAGGTAAAAGAGATAGCGAGAAAGGGGGGCGGTGATTGTCGAGTAATTGTCAATGGGCCATTTGGTTCACAGCAGGCTTGTGAGACTGCATCCTTTGAACAATAGGTGCTAGATTTCTCAATAGATAACTTCAAGGAGCCCAGCGCCAAGGAGTGATGTCCCTCAGCAAACCTTTTGGTGGCAGGCGCAGTGTGAGTTTGTTCACATCTTGCATTCATGATAAACAGTTTGCTGTTTGATCATATAGCCTCAAGTGGAGCGCTGAGTTGGTC... |
Task1_train_33296 | Consider this mutation on Chromosome 1. Is this a benign change or a disease-causing variant? | Benign | GTCAGGCCCGGCCCTAGCTCTGGAGGTGGTTGGATTGGTTCAAGGGCTGCAGCCCCACCTCGCGTCTTCCCACCGCGTCGGAGGACGTAGGCGCCTGGGATCCTGGAAGGCGGCCAGCCTCTGCAGCCGGGCCCAGCGGCTCCTGAGACTGGGGCGGACCTCACACCTGACCCCGGAGCGGCTAATCCTGCCCAACCGTCCCACCTGCCACGTGCCCTCGGGGCTGGAACGCGGCGCCCCGGGAGAGGCCTGCTGGTCAGGGGGCGCTGGTGCGCAGGCGCGCGGGGCCGCCGTCGCAGCTACCTTCCTGCGCCGATTCG... | GTCAGGCCCGGCCCTAGCTCTGGAGGTGGTTGGATTGGTTCAAGGGCTGCAGCCCCACCTCGCGTCTTCCCACCGCGTCGGAGGACGTAGGCGCCTGGGATCCTGGAAGGCGGCCAGCCTCTGCAGCCGGGCCCAGCGGCTCCTGAGACTGGGGCGGACCTCACACCTGACCCCGGAGCGGCTAATCCTGCCCAACCGTCCCACCTGCCACGTGCCCTCGGGGCTGGAACGCGGCGCCCCGGGAGAGGCCTGCTGGTCAGGGGGCGCTGGTGCGCAGGCGCGCGGGGCCGCCGTCGCAGCTACCTTCCTGCGCCGATTCG... |
Task1_train_33297 | This genomic variant is located on Chromosome 1. Can you determine its pathogenicity and name any linked disease? | Benign | CCCCACCTCGCGTCTTCCCACCGCGTCGGAGGACGTAGGCGCCTGGGATCCTGGAAGGCGGCCAGCCTCTGCAGCCGGGCCCAGCGGCTCCTGAGACTGGGGCGGACCTCACACCTGACCCCGGAGCGGCTAATCCTGCCCAACCGTCCCACCTGCCACGTGCCCTCGGGGCTGGAACGCGGCGCCCCGGGAGAGGCCTGCTGGTCAGGGGGCGCTGGTGCGCAGGCGCGCGGGGCCGCCGTCGCAGCTACCTTCCTGCGCCGATTCGGAGAGGGCCCCCTAATCTCTACTCGGCCCGCACCAGCAGCGCTGGCGTCAGG... | CCCCACCTCGCGTCTTCCCACCGCGTCGGAGGACGTAGGCGCCTGGGATCCTGGAAGGCGGCCAGCCTCTGCAGCCGGGCCCAGCGGCTCCTGAGACTGGGGCGGACCTCACACCTGACCCCGGAGCGGCTAATCCTGCCCAACCGTCCCACCTGCCACGTGCCCTCGGGGCTGGAACGCGGCGCCCCGGGAGAGGCCTGCTGGTCAGGGGGCGCTGGTGCGCAGGCGCGCGGGGCCGCCGTCGCAGCTACCTTCCTGCGCCGATTCGGAGAGGGCCCCCTAATCTCTACTCGGCCCGCACCAGCAGCGCTGGCGTCAGG... |
Task1_train_33298 | A variant was discovered on Chromosome 1. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TGTTGAATCATATTTGAGTTTTGATAATTTCTGGAACATTTTAACAAGGAACTGGCAATAATGGTTACTTCCAGGGAAGTGATTGCTAGGTGACTGAGGAATTTGTTGTTGTTGTTGTTGTTGTTGTTTTTGCCAATTTAACTGAAGTGTTTATTTTTAAAATAGTTCCTGATTAAACTCACATCCTGCCTTTTAATAATCAGATCACTCAGCATCATCACAGTTTACCAAAATACAGATAAATTCTAAAGGAAAATGTCATTTCTGAATAAGAGCTGTCAAGTCAAAGTGATTGAGAAATCCAGATGAGCACTATTTCT... | TGTTGAATCATATTTGAGTTTTGATAATTTCTGGAACATTTTAACAAGGAACTGGCAATAATGGTTACTTCCAGGGAAGTGATTGCTAGGTGACTGAGGAATTTGTTGTTGTTGTTGTTGTTGTTGTTTTTGCCAATTTAACTGAAGTGTTTATTTTTAAAATAGTTCCTGATTAAACTCACATCCTGCCTTTTAATAATCAGATCACTCAGCATCATCACAGTTTACCAAAATACAGATAAATTCTAAAGGAAAATGTCATTTCTGAATAAGAGCTGTCAAGTCAAAGTGATTGAGAAATCCAGATGAGCACTATTTCT... |
Task1_train_33299 | This variant is present on Chromosome 1. Is the change likely to result in a pathogenic outcome? | Benign | TTATGTTTAATGTGATTATATATATGTTTTTATTTTAGATCTGCCATTTTATTTTTCTGTTTGTTCCCCTGATTTTCATTCATCTGCCTCCTCTTTCTTGCCTTCTCTTAGGTTATTTGAACATTTTTTAGTATTCCATTTTATCTACTATGGTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTTGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCACAATCTCGGCTCACTGCAAGCTCTGCCTCTCAGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTCCAGGCACCCACCAGCACAC... | TTATGTTTAATGTGATTATATATATGTTTTTATTTTAGATCTGCCATTTTATTTTTCTGTTTGTTCCCCTGATTTTCATTCATCTGCCTCCTCTTTCTTGCCTTCTCTTAGGTTATTTGAACATTTTTTAGTATTCCATTTTATCTACTATGGTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTTGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCACAATCTCGGCTCACTGCAAGCTCTGCCTCTCAGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTCCAGGCACCCACCAGCACAC... |
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