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_46400 | This sequence variant lies on Chromosome 19. Is it clinically significant, and what condition might it cause if any? | Benign | CAGAAGACCCGTGCGCCAAGGATGGAGGACGCCGGCGAGGGTGGGTGGGACTTTTTCCCGCCCCCCATCAGCTTCCGGGCGCCTAGTTCAGTTTCTCCCGGGTCTGTCTGCCCCTAGAGTTGGGGGCACCCAACTTGGCTTCTCCGCGTCCCCTACTATCATCCCCAGATTCACTGTTGGGGAGAAGCCCGCTCCGAGGTGAACGGTGAAAGGGGCGCAAGGTTTATACGGGAACGCCGGCGCAGATGAAGGCGCAGGTGCCAGTCATTTTTAAGGCAAAAATCCTGTATTTCGGGACGGTGGCATTTGTGCCCCCTGGG... | CAGAAGACCCGTGCGCCAAGGATGGAGGACGCCGGCGAGGGTGGGTGGGACTTTTTCCCGCCCCCCATCAGCTTCCGGGCGCCTAGTTCAGTTTCTCCCGGGTCTGTCTGCCCCTAGAGTTGGGGGCACCCAACTTGGCTTCTCCGCGTCCCCTACTATCATCCCCAGATTCACTGTTGGGGAGAAGCCCGCTCCGAGGTGAACGGTGAAAGGGGCGCAAGGTTTATACGGGAACGCCGGCGCAGATGAAGGCGCAGGTGCCAGTCATTTTTAAGGCAAAAATCCTGTATTTCGGGACGGTGGCATTTGTGCCCCCTGGG... |
Task1_train_46401 | A variant on Chromosome 19 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | CGAGGGTGGGTGGGACTTTTTCCCGCCCCCCATCAGCTTCCGGGCGCCTAGTTCAGTTTCTCCCGGGTCTGTCTGCCCCTAGAGTTGGGGGCACCCAACTTGGCTTCTCCGCGTCCCCTACTATCATCCCCAGATTCACTGTTGGGGAGAAGCCCGCTCCGAGGTGAACGGTGAAAGGGGCGCAAGGTTTATACGGGAACGCCGGCGCAGATGAAGGCGCAGGTGCCAGTCATTTTTAAGGCAAAAATCCTGTATTTCGGGACGGTGGCATTTGTGCCCCCTGGGAAGGGGATGAGCACTGCTGCCTCCTGGTATCCACC... | CGAGGGTGGGTGGGACTTTTTCCCGCCCCCCATCAGCTTCCGGGCGCCTAGTTCAGTTTCTCCCGGGTCTGTCTGCCCCTAGAGTTGGGGGCACCCAACTTGGCTTCTCCGCGTCCCCTACTATCATCCCCAGATTCACTGTTGGGGAGAAGCCCGCTCCGAGGTGAACGGTGAAAGGGGCGCAAGGTTTATACGGGAACGCCGGCGCAGATGAAGGCGCAGGTGCCAGTCATTTTTAAGGCAAAAATCCTGTATTTCGGGACGGTGGCATTTGTGCCCCCTGGGAAGGGGATGAGCACTGCTGCCTCCTGGTATCCACC... |
Task1_train_46402 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TTTCTTAAATGCCTGATTGTACAACCATCCTCCTACCAGTCTGATCGTAAATCTGGCCTTTTGGCTGTATAACTGCTGGAGTATCTGATACAACCACCACACCGTCTAACTGTCTGATCAGATGATAATCCTAGAGAAGGAATGGTTTTATACCTGAACACCTTTCTGGCTGTCTTACTCAGTGCTGGGCTAGGTGACTATAGCAGGGATAAGATTATTCCATAGCTCCACTGGTTCGCCGTCTGAGGATATGTCTCTGCTGTCCCCTGGATAGAACTCCCTATTTTTTCTTTTTGAGACGGAGTCTTGCTGTGTCGCCC... | TTTCTTAAATGCCTGATTGTACAACCATCCTCCTACCAGTCTGATCGTAAATCTGGCCTTTTGGCTGTATAACTGCTGGAGTATCTGATACAACCACCACACCGTCTAACTGTCTGATCAGATGATAATCCTAGAGAAGGAATGGTTTTATACCTGAACACCTTTCTGGCTGTCTTACTCAGTGCTGGGCTAGGTGACTATAGCAGGGATAAGATTATTCCATAGCTCCACTGGTTCGCCGTCTGAGGATATGTCTCTGCTGTCCCCTGGATAGAACTCCCTATTTTTTCTTTTTGAGACGGAGTCTTGCTGTGTCGCCC... |
Task1_train_46403 | An alteration has been detected on Chromosome 19. Is it pathogenic, and if so, what disease is involved? | Benign | TCATTCATGTGTTCATTCATTAAGTCATTAATTCATTCAACAAGTGTTTATTTACCACCTGCTATTTACAAGCACAATGTTAGGTACCAGGGATACAAGAGTAGACCAAAAAAGACATACATATGCCCTTATGGAGATGACAGTCATCGGTTTTCAGAACAAAGATGATCGGTTTTCAGCCCTCAGTGCCCCTTCTTTCCTGAAGTTTGTTCTGAATTTTTAGACAGGCTCCTTCCGCCTTGCTGTGGTTTTTCTCTCCACCTGTTTTGTATCTGAATCACAGAAGGTGAAGACATCCCCCAGGTGGTTAGTAGAACCCA... | TCATTCATGTGTTCATTCATTAAGTCATTAATTCATTCAACAAGTGTTTATTTACCACCTGCTATTTACAAGCACAATGTTAGGTACCAGGGATACAAGAGTAGACCAAAAAAGACATACATATGCCCTTATGGAGATGACAGTCATCGGTTTTCAGAACAAAGATGATCGGTTTTCAGCCCTCAGTGCCCCTTCTTTCCTGAAGTTTGTTCTGAATTTTTAGACAGGCTCCTTCCGCCTTGCTGTGGTTTTTCTCTCCACCTGTTTTGTATCTGAATCACAGAAGGTGAAGACATCCCCCAGGTGGTTAGTAGAACCCA... |
Task1_train_46404 | A variant found on Chromosome 19 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | ACATACATATGCCCTTATGGAGATGACAGTCATCGGTTTTCAGAACAAAGATGATCGGTTTTCAGCCCTCAGTGCCCCTTCTTTCCTGAAGTTTGTTCTGAATTTTTAGACAGGCTCCTTCCGCCTTGCTGTGGTTTTTCTCTCCACCTGTTTTGTATCTGAATCACAGAAGGTGAAGACATCCCCCAGGTGGTTAGTAGAACCCAGATCTTTGTGTTAGAGTCTTCATGAAAACCAGTGTGAGAAACTGGGCTGAGGCAAGGGAGGTAGTCTTCCATCCTTGCTATATCTCTGGGACACTGGGCATCTTTTCTGGGCTC... | ACATACATATGCCCTTATGGAGATGACAGTCATCGGTTTTCAGAACAAAGATGATCGGTTTTCAGCCCTCAGTGCCCCTTCTTTCCTGAAGTTTGTTCTGAATTTTTAGACAGGCTCCTTCCGCCTTGCTGTGGTTTTTCTCTCCACCTGTTTTGTATCTGAATCACAGAAGGTGAAGACATCCCCCAGGTGGTTAGTAGAACCCAGATCTTTGTGTTAGAGTCTTCATGAAAACCAGTGTGAGAAACTGGGCTGAGGCAAGGGAGGTAGTCTTCCATCCTTGCTATATCTCTGGGACACTGGGCATCTTTTCTGGGCTC... |
Task1_train_46405 | The following genetic variant occurs on Chromosome 19. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GCTCCTTCCGCCTTGCTGTGGTTTTTCTCTCCACCTGTTTTGTATCTGAATCACAGAAGGTGAAGACATCCCCCAGGTGGTTAGTAGAACCCAGATCTTTGTGTTAGAGTCTTCATGAAAACCAGTGTGAGAAACTGGGCTGAGGCAAGGGAGGTAGTCTTCCATCCTTGCTATATCTCTGGGACACTGGGCATCTTTTCTGGGCTCCACCCTAGGGGTTGGGAATCTAATAACTTTGATTTTTTTTCTCTACCCCCAATTACCAACCCTCTAATTCTTCAACACTAGGCACATGGGAATTGTGTTTTGTTTTCAAACCT... | GCTCCTTCCGCCTTGCTGTGGTTTTTCTCTCCACCTGTTTTGTATCTGAATCACAGAAGGTGAAGACATCCCCCAGGTGGTTAGTAGAACCCAGATCTTTGTGTTAGAGTCTTCATGAAAACCAGTGTGAGAAACTGGGCTGAGGCAAGGGAGGTAGTCTTCCATCCTTGCTATATCTCTGGGACACTGGGCATCTTTTCTGGGCTCCACCCTAGGGGTTGGGAATCTAATAACTTTGATTTTTTTTCTCTACCCCCAATTACCAACCCTCTAATTCTTCAACACTAGGCACATGGGAATTGTGTTTTGTTTTCAAACCT... |
Task1_train_46406 | This alteration on Chromosome 19 may affect genome function. Does it lead to a disease or is it benign? | Benign | ACTGGGCTGAGGCAAGGGAGGTAGTCTTCCATCCTTGCTATATCTCTGGGACACTGGGCATCTTTTCTGGGCTCCACCCTAGGGGTTGGGAATCTAATAACTTTGATTTTTTTTCTCTACCCCCAATTACCAACCCTCTAATTCTTCAACACTAGGCACATGGGAATTGTGTTTTGTTTTCAAACCTGGGCAACAAAGTGAGACCATGTTCCTACAGAAAATTTAAAAATAGCTGAGCATAATGGCATACAAGTGTAGTCCCAGCTACTTGGGAAGCTGAGGCATGATGATTGCCTGAGCCCAACAGTTCAAGGCTGCAG... | ACTGGGCTGAGGCAAGGGAGGTAGTCTTCCATCCTTGCTATATCTCTGGGACACTGGGCATCTTTTCTGGGCTCCACCCTAGGGGTTGGGAATCTAATAACTTTGATTTTTTTTCTCTACCCCCAATTACCAACCCTCTAATTCTTCAACACTAGGCACATGGGAATTGTGTTTTGTTTTCAAACCTGGGCAACAAAGTGAGACCATGTTCCTACAGAAAATTTAAAAATAGCTGAGCATAATGGCATACAAGTGTAGTCCCAGCTACTTGGGAAGCTGAGGCATGATGATTGCCTGAGCCCAACAGTTCAAGGCTGCAG... |
Task1_train_46407 | This mutation occurs on Chromosome 19. Does this change lead to a known medical condition, or is it benign? | Benign | GGTGGATTTGGGGTGCTGAGAACCAGGGGTATCTTGACAAGTGGAATCTTGACAAGTGGAATTTAAGAGTGTGTTTGGGGGGATTAGAAATAAGGGGAAGATTATGGGGGTGCACCCAGGGGTTGGAGCACTCACGGGAAGATTCTGGGAGGAGGTTGGAGCATTCCGGGGTAGAGACTGGGTTGGGGGGTCCCTGAGGAGCATACTAAGGGGGGTGGCAGTTTGGAGGGTTTGGAGCCCAGGGGTATTTTGGGATGCTATATCAAAAGCAATAGATAATGGGGTGAGATTAGGGAGTCAGTATTTGAGGATGTCTTGGG... | GGTGGATTTGGGGTGCTGAGAACCAGGGGTATCTTGACAAGTGGAATCTTGACAAGTGGAATTTAAGAGTGTGTTTGGGGGGATTAGAAATAAGGGGAAGATTATGGGGGTGCACCCAGGGGTTGGAGCACTCACGGGAAGATTCTGGGAGGAGGTTGGAGCATTCCGGGGTAGAGACTGGGTTGGGGGGTCCCTGAGGAGCATACTAAGGGGGGTGGCAGTTTGGAGGGTTTGGAGCCCAGGGGTATTTTGGGATGCTATATCAAAAGCAATAGATAATGGGGTGAGATTAGGGAGTCAGTATTTGAGGATGTCTTGGG... |
Task1_train_46408 | Given this variant on Chromosome 19, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TTTTTTTTTTTTTTGGTAGAGATGGGGTTTCACCATGTTGGCCAGCCTGGTCTTGAACTCCTGGCCTCAAGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGAGATTACAGGCGTGGAGCCACCGTGCCCGGCCTCTAAGGGAAATATTGAGGTCGCAGACCACAGAATCCAAGAGTGCTAGGAATCAGAGGAGAGAGAGGAAGGTGAAGATACGGAGGTCCGGAGTAATTCAAATACCCAAATCACAGATACTTGCTCCTCAAGGTATGTTCATCAAGAACAGGTATCTATGGTATGGGCATTTGAATTAAAAAACCT... | TTTTTTTTTTTTTTGGTAGAGATGGGGTTTCACCATGTTGGCCAGCCTGGTCTTGAACTCCTGGCCTCAAGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGAGATTACAGGCGTGGAGCCACCGTGCCCGGCCTCTAAGGGAAATATTGAGGTCGCAGACCACAGAATCCAAGAGTGCTAGGAATCAGAGGAGAGAGAGGAAGGTGAAGATACGGAGGTCCGGAGTAATTCAAATACCCAAATCACAGATACTTGCTCCTCAAGGTATGTTCATCAAGAACAGGTATCTATGGTATGGGCATTTGAATTAAAAAACCT... |
Task1_train_46409 | This variant is present on Chromosome 19. Is the change likely to result in a pathogenic outcome? | Benign | CCCTTCATTTCTCTCTCCTTTTGCCTCTGAATTTCTTTATCAATATATCACATATCTACCAATGATCTATTTATCTATCATCTAGCTATCAATATTTATCAACCTGTCAATCAATTATCTACCAATCAATAACCATCAATTATCTCTCACCTCTCAATCATCTCCTATTTATAATCCATCAATCATCTATCAATCACCTGTCATCCATCAATCATGTATTTATCATCTACTTATCAATATCTATCAACTATCTGTTACCTATCAATTTATTATCTACCAATTATCTATCAAAATAATCTATTTATCATCTACCTATCAGC... | CCCTTCATTTCTCTCTCCTTTTGCCTCTGAATTTCTTTATCAATATATCACATATCTACCAATGATCTATTTATCTATCATCTAGCTATCAATATTTATCAACCTGTCAATCAATTATCTACCAATCAATAACCATCAATTATCTCTCACCTCTCAATCATCTCCTATTTATAATCCATCAATCATCTATCAATCACCTGTCATCCATCAATCATGTATTTATCATCTACTTATCAATATCTATCAACTATCTGTTACCTATCAATTTATTATCTACCAATTATCTATCAAAATAATCTATTTATCATCTACCTATCAGC... |
Task1_train_46410 | A genomic change on Chromosome 19 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GGCACGAGAATCGCTTGAACTCAGGAGGCAGAGTTTGCAGTGAGCCAAGATTGCACCACTGTACTCCAGCTTGAGCGACAGAGTCAGACTCTGTCTCAGAAAAAAAAAAAAGAGAAGAAAGAAAGAAATGAAACCAGTATCTTAAAGAGATATCTGCACTCCTATGTTCATTGCAGCACTATTCAAAATAGCCAAGATATGGAAACAAGCTAAATGACCTTCAATGGATGAATGGGTAAAGAAAATGTGGCATACACATATACAATGAAATATATAAGAAAGATGAAAATCCTGCCACTTGGGATAACATAGATGGAGCT... | GGCACGAGAATCGCTTGAACTCAGGAGGCAGAGTTTGCAGTGAGCCAAGATTGCACCACTGTACTCCAGCTTGAGCGACAGAGTCAGACTCTGTCTCAGAAAAAAAAAAAAGAGAAGAAAGAAAGAAATGAAACCAGTATCTTAAAGAGATATCTGCACTCCTATGTTCATTGCAGCACTATTCAAAATAGCCAAGATATGGAAACAAGCTAAATGACCTTCAATGGATGAATGGGTAAAGAAAATGTGGCATACACATATACAATGAAATATATAAGAAAGATGAAAATCCTGCCACTTGGGATAACATAGATGGAGCT... |
Task1_train_46411 | This is a variant located on Chromosome 19. Is this mutation a likely cause of disease or not? | Benign | TAGGGCCTGAAGTGAACCCCTAGCAAACTGCAGCAGCCCTACAGAAGAGGGACCTGACTATTGAAAGAAAAACAAGCAGAAAGTGACAATAACATCATCATCATCAACAACAACAACCAAAAGACCCCCATAAAAACCCCATCCAAGGATCAGCAGCCTCAAAGCCTGAAACTAAAACTCCTGAAGATGGGAAATAATCAACAAAAAAATGCTGAAAACCCAAAAGGCCAGAGTGCCTCTTTTCCTCCAAATGACCGCAACATCTCTCCATTAAGGGTGCAGAACTGGATGGAGGATCAGATGGATGAATTGACAGAAGT... | TAGGGCCTGAAGTGAACCCCTAGCAAACTGCAGCAGCCCTACAGAAGAGGGACCTGACTATTGAAAGAAAAACAAGCAGAAAGTGACAATAACATCATCATCATCAACAACAACAACCAAAAGACCCCCATAAAAACCCCATCCAAGGATCAGCAGCCTCAAAGCCTGAAACTAAAACTCCTGAAGATGGGAAATAATCAACAAAAAAATGCTGAAAACCCAAAAGGCCAGAGTGCCTCTTTTCCTCCAAATGACCGCAACATCTCTCCATTAAGGGTGCAGAACTGGATGGAGGATCAGATGGATGAATTGACAGAAGT... |
Task1_train_46412 | This mutation on Chromosome 19 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TTGTAGCATGGGGTAAGGAGAACTCATACTTGAGACAGGTGAAGAGCTAGGTTTGGGGATGAAAGCAAGTGGACGAGGCATGTTTTTCTTGGGAGAAATCCTGGGAACAGAATTGAACCACTTGTGGAAAGGCAGGTAGGGGAAAGGAGGGAATTCAGAGGGATGACCAAGGTAGAAGCTCAGTCCTGCTGATGGGCTCTGCATCTCTCAGTTGAGGTGGGAGGTGGTGGGAACAGGAAGCACATTGGTCTTAGAGCCACTGCCTCCTGGATTCCACCTGGCTGCGGACATCTCCAGGGAGTGCAGAAGGGAAGCAGGTC... | TTGTAGCATGGGGTAAGGAGAACTCATACTTGAGACAGGTGAAGAGCTAGGTTTGGGGATGAAAGCAAGTGGACGAGGCATGTTTTTCTTGGGAGAAATCCTGGGAACAGAATTGAACCACTTGTGGAAAGGCAGGTAGGGGAAAGGAGGGAATTCAGAGGGATGACCAAGGTAGAAGCTCAGTCCTGCTGATGGGCTCTGCATCTCTCAGTTGAGGTGGGAGGTGGTGGGAACAGGAAGCACATTGGTCTTAGAGCCACTGCCTCCTGGATTCCACCTGGCTGCGGACATCTCCAGGGAGTGCAGAAGGGAAGCAGGTC... |
Task1_train_46413 | Given a variant located on Chromosome 19, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | CCTCTACTAAAAATATAAAAATTAGCTGGGCATGGTGGCATGCACCTGTAATCCCAGCTACTCAGGAGGTGGAGGCAGGAGAATCGCTTGAACCTAGGAGGCAGAGGTTGCAGTGGGCTGAGATCACGCCATTGCATTCTAGCCTGGGTGACAGAGCAAGACTATGTCTCAAAAAAGAAAAAAAAGAAAGAAAAGAAAATGGCAGAGATGTTGACACTCCTCAGGCATGCTGTAATAGAGATGACACTGAATAGTACTCACTCATGGGTCCAGACAGGGAGGCTGGAGTTCTCGAGGTTGCCAGGTGCATTGTGGAGGTA... | CCTCTACTAAAAATATAAAAATTAGCTGGGCATGGTGGCATGCACCTGTAATCCCAGCTACTCAGGAGGTGGAGGCAGGAGAATCGCTTGAACCTAGGAGGCAGAGGTTGCAGTGGGCTGAGATCACGCCATTGCATTCTAGCCTGGGTGACAGAGCAAGACTATGTCTCAAAAAAGAAAAAAAAGAAAGAAAAGAAAATGGCAGAGATGTTGACACTCCTCAGGCATGCTGTAATAGAGATGACACTGAATAGTACTCACTCATGGGTCCAGACAGGGAGGCTGGAGTTCTCGAGGTTGCCAGGTGCATTGTGGAGGTA... |
Task1_train_46414 | This mutation occurs on Chromosome 19. Does this change lead to a known medical condition, or is it benign? | Benign | GGGCATGGTGGCATGCACCTGTAATCCCAGCTACTCAGGAGGTGGAGGCAGGAGAATCGCTTGAACCTAGGAGGCAGAGGTTGCAGTGGGCTGAGATCACGCCATTGCATTCTAGCCTGGGTGACAGAGCAAGACTATGTCTCAAAAAAGAAAAAAAAGAAAGAAAAGAAAATGGCAGAGATGTTGACACTCCTCAGGCATGCTGTAATAGAGATGACACTGAATAGTACTCACTCATGGGTCCAGACAGGGAGGCTGGAGTTCTCGAGGTTGCCAGGTGCATTGTGGAGGTATCAGGAGCTGAGGAGAAGGTTTGCTGT... | GGGCATGGTGGCATGCACCTGTAATCCCAGCTACTCAGGAGGTGGAGGCAGGAGAATCGCTTGAACCTAGGAGGCAGAGGTTGCAGTGGGCTGAGATCACGCCATTGCATTCTAGCCTGGGTGACAGAGCAAGACTATGTCTCAAAAAAGAAAAAAAAGAAAGAAAAGAAAATGGCAGAGATGTTGACACTCCTCAGGCATGCTGTAATAGAGATGACACTGAATAGTACTCACTCATGGGTCCAGACAGGGAGGCTGGAGTTCTCGAGGTTGCCAGGTGCATTGTGGAGGTATCAGGAGCTGAGGAGAAGGTTTGCTGT... |
Task1_train_46415 | The following genetic variant occurs on Chromosome 19. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | ACCCAGGCTGGCTCTTCTAAAGTCTCACCTGAGCAAGGTCAGTCTGCAGCCAGAGTACAGAAGGCCAACACTGGTGTTCTTGAACATAGGACCAAGCTGTAGAGGAGGGAGAGGGAGGTGAGTAGTGGGGCTAAGGTGTGTGTGTGTCGGGGCAGATGTGAGGTGGGTGGAGCAGGCACCAATAAGCAGGACTGGTCTCTGTGGGTGGGGCTTGCATCTCTTGGGGGGAAGGGGGGAAGTTGTTGCTATCTTCTTTCATCACCCTGGCATGGATGATGTAGAAGGGACTGGATATCTGGGGCTGGGCAGAGTGAGGAGGG... | ACCCAGGCTGGCTCTTCTAAAGTCTCACCTGAGCAAGGTCAGTCTGCAGCCAGAGTACAGAAGGCCAACACTGGTGTTCTTGAACATAGGACCAAGCTGTAGAGGAGGGAGAGGGAGGTGAGTAGTGGGGCTAAGGTGTGTGTGTGTCGGGGCAGATGTGAGGTGGGTGGAGCAGGCACCAATAAGCAGGACTGGTCTCTGTGGGTGGGGCTTGCATCTCTTGGGGGGAAGGGGGGAAGTTGTTGCTATCTTCTTTCATCACCCTGGCATGGATGATGTAGAAGGGACTGGATATCTGGGGCTGGGCAGAGTGAGGAGGG... |
Task1_train_46416 | This mutation occurs on Chromosome 19. Does this change lead to a known medical condition, or is it benign? | Benign | ATGGCAACAAAAGCCAAAATTGACAAATGGGATCTAATTAAACTAAAGAGCTTCTGCACAGCAAAAGAAACTACCATTGGAGTGAACAGGCAACCTATAAAATGGGAGAAAATTTTCACAACCTACTCATCTGACAAAGGGCTAATATCCAGAATCTACAATGAACTCAAACACATTTACAAGGAAAAAGCAAACAACCCCAACAAAAAGTGGGAGAAGGACATGAACAGACACTTCTCAAAAGAAGACATTTATGCAGCCAAAAAACACATGAAAAAATGCTCACCATCACTGGCTATCAGAGAAATGCAAATCAAAAC... | ATGGCAACAAAAGCCAAAATTGACAAATGGGATCTAATTAAACTAAAGAGCTTCTGCACAGCAAAAGAAACTACCATTGGAGTGAACAGGCAACCTATAAAATGGGAGAAAATTTTCACAACCTACTCATCTGACAAAGGGCTAATATCCAGAATCTACAATGAACTCAAACACATTTACAAGGAAAAAGCAAACAACCCCAACAAAAAGTGGGAGAAGGACATGAACAGACACTTCTCAAAAGAAGACATTTATGCAGCCAAAAAACACATGAAAAAATGCTCACCATCACTGGCTATCAGAGAAATGCAAATCAAAAC... |
Task1_train_46417 | Here is a genetic alteration on Chromosome 19. Based on the data, is it a benign variant or a cause of disease? | Benign | GAGTGTGAAATAAACATTATGTTCAAAGTAGAGAGAATAGCACTTTGTAATAACCATATGCAGCAATTAAATTGAGTGACATAATAAATATTTTCCACGCCTTTCTTATCTATGATACAATTCATTTTCTAAAGTAGATTATATAATAGTAGTTAGATACTGAGCATAGCTCTTGGTACATATTTAGTGCTCAATATTGTAAGGTGATATCTGTTATCTTTATTATCACCATCACCATCATCACTATCATTGTCATCATTATTATCATTATTGTCATCACAAGTACCACCAGCACCACCATGACAATCCCCATCATGAAC... | GAGTGTGAAATAAACATTATGTTCAAAGTAGAGAGAATAGCACTTTGTAATAACCATATGCAGCAATTAAATTGAGTGACATAATAAATATTTTCCACGCCTTTCTTATCTATGATACAATTCATTTTCTAAAGTAGATTATATAATAGTAGTTAGATACTGAGCATAGCTCTTGGTACATATTTAGTGCTCAATATTGTAAGGTGATATCTGTTATCTTTATTATCACCATCACCATCATCACTATCATTGTCATCATTATTATCATTATTGTCATCACAAGTACCACCAGCACCACCATGACAATCCCCATCATGAAC... |
Task1_train_46418 | This genomic variant is located on Chromosome 19. Can you determine its pathogenicity and name any linked disease? | Benign | TTGACATTTTGGTCTGGATAATGTGTTTTGATAGGAGGCTGCTTTGTGCATTGTTGGATGTTTTGCAACATCTCTGGCCTCTACTTACTAGATGCCATTAGCAAATGGCCGGGCATCATGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCGGATCACCTGAAGTCAGGAGTTCAAGAGCAGCCTGGCGAACATGGAGAAACCTCATCTCTACTAAAAATACAAAATTAGCTGGGCATGGTGGCACATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCA... | TTGACATTTTGGTCTGGATAATGTGTTTTGATAGGAGGCTGCTTTGTGCATTGTTGGATGTTTTGCAACATCTCTGGCCTCTACTTACTAGATGCCATTAGCAAATGGCCGGGCATCATGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCGGATCACCTGAAGTCAGGAGTTCAAGAGCAGCCTGGCGAACATGGAGAAACCTCATCTCTACTAAAAATACAAAATTAGCTGGGCATGGTGGCACATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCA... |
Task1_train_46419 | This mutation occurs on Chromosome 19. Does this change lead to a known medical condition, or is it benign? | Benign | ACCCTGTCTGTACTAAAAATACAAAAATTAGCCAGGCACGGTGGCGTGCACCTGTAGTCCCAACTACTCAGGAGGCTGATGCAGGAGAATTGCTTGAACCCAGGAGACAGAGGTTCAGAGGTTGTGGTGAGCCGAGATTGCACCACTGCACTAGGGAGAATGGGGAATGGGAAATTATTCCTTCAGTCCTGTTTGGGGTGATAAAAAAAGTTTTGAAAACAGATAGTGGTGAGGGTTGCACAACAATGTGAATGTATTAGTACTGCTGAGTTGTACAATTAAAATGTTTAGAATGGCAATTTTTATAGTATTTATATTTT... | ACCCTGTCTGTACTAAAAATACAAAAATTAGCCAGGCACGGTGGCGTGCACCTGTAGTCCCAACTACTCAGGAGGCTGATGCAGGAGAATTGCTTGAACCCAGGAGACAGAGGTTCAGAGGTTGTGGTGAGCCGAGATTGCACCACTGCACTAGGGAGAATGGGGAATGGGAAATTATTCCTTCAGTCCTGTTTGGGGTGATAAAAAAAGTTTTGAAAACAGATAGTGGTGAGGGTTGCACAACAATGTGAATGTATTAGTACTGCTGAGTTGTACAATTAAAATGTTTAGAATGGCAATTTTTATAGTATTTATATTTT... |
Task1_train_46420 | Located on Chromosome 19, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | AGCTGGTGGCCAGTAAGCCTGTAGTCTCTAGTAAACCAAGGGAAAGAGTTGAAGTTGGAATCATTGTGCTGGTTTCTGTCCCTGGATGGGTGGAAAGTGGGGCTGTTTTTGCAGAAACACCAGGTGAAGCAGTTGGACTTAGATCAACTCTGCTGGTTCCAGTTACAAGTAGGGTGAAGAGAGAGGATGTTGTCTGAGTTGGGAGAGCTGTGCTAGTCTCTGCACCAGGTCTAATGGTGAGTGAGGCTGTGGTCTCTGATACTTGAGGAAACACAGTTGAAGCAGGAAATGTTTTACTTGTCTCTGTTCTGGGATGGGTG... | AGCTGGTGGCCAGTAAGCCTGTAGTCTCTAGTAAACCAAGGGAAAGAGTTGAAGTTGGAATCATTGTGCTGGTTTCTGTCCCTGGATGGGTGGAAAGTGGGGCTGTTTTTGCAGAAACACCAGGTGAAGCAGTTGGACTTAGATCAACTCTGCTGGTTCCAGTTACAAGTAGGGTGAAGAGAGAGGATGTTGTCTGAGTTGGGAGAGCTGTGCTAGTCTCTGCACCAGGTCTAATGGTGAGTGAGGCTGTGGTCTCTGATACTTGAGGAAACACAGTTGAAGCAGGAAATGTTTTACTTGTCTCTGTTCTGGGATGGGTG... |
Task1_train_46421 | The following genetic variant occurs on Chromosome 19. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GACTTAGATCAACTCTGCTGGTTCCAGTTACAAGTAGGGTGAAGAGAGAGGATGTTGTCTGAGTTGGGAGAGCTGTGCTAGTCTCTGCACCAGGTCTAATGGTGAGTGAGGCTGTGGTCTCTGATACTTGAGGAAACACAGTTGAAGCAGGAAATGTTTTACTTGTCTCTGTTCTGGGATGGGTGCTCAATAAGGCTGTGGTCTCTGGCATACCAGGAGAATGAGTCAAAGTTGGAACAGTTGTACTGGTTGCTGCCCCAGAACTAGTGATCTGTGAAGTCACCATCTCTGGTGCACCAGGTGAGATTGTTGTCAGTACA... | GACTTAGATCAACTCTGCTGGTTCCAGTTACAAGTAGGGTGAAGAGAGAGGATGTTGTCTGAGTTGGGAGAGCTGTGCTAGTCTCTGCACCAGGTCTAATGGTGAGTGAGGCTGTGGTCTCTGATACTTGAGGAAACACAGTTGAAGCAGGAAATGTTTTACTTGTCTCTGTTCTGGGATGGGTGCTCAATAAGGCTGTGGTCTCTGGCATACCAGGAGAATGAGTCAAAGTTGGAACAGTTGTACTGGTTGCTGCCCCAGAACTAGTGATCTGTGAAGTCACCATCTCTGGTGCACCAGGTGAGATTGTTGTCAGTACA... |
Task1_train_46422 | This sequence change occurs on Chromosome 19. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GAAATGTTTTACTTGTCTCTGTTCTGGGATGGGTGCTCAATAAGGCTGTGGTCTCTGGCATACCAGGAGAATGAGTCAAAGTTGGAACAGTTGTACTGGTTGCTGCCCCAGAACTAGTGATCTGTGAAGTCACCATCTCTGGTGCACCAGGTGAGATTGTTGTCAGTACAGCTGAACTGGCTTCTGTCCTAGGACTGGTGGCCATTACAGGTGTGGCATCTGGACTACTATGGGAAAAACTGGAGGTTGTTCTGGAAACAGGTGTGCTGGTCTGTGGAGGATGAGTGACCCAGGAAGCCATTGTATCTGGCTCACTAGAG... | GAAATGTTTTACTTGTCTCTGTTCTGGGATGGGTGCTCAATAAGGCTGTGGTCTCTGGCATACCAGGAGAATGAGTCAAAGTTGGAACAGTTGTACTGGTTGCTGCCCCAGAACTAGTGATCTGTGAAGTCACCATCTCTGGTGCACCAGGTGAGATTGTTGTCAGTACAGCTGAACTGGCTTCTGTCCTAGGACTGGTGGCCATTACAGGTGTGGCATCTGGACTACTATGGGAAAAACTGGAGGTTGTTCTGGAAACAGGTGTGCTGGTCTGTGGAGGATGAGTGACCCAGGAAGCCATTGTATCTGGCTCACTAGAG... |
Task1_train_46423 | This variant is found on Chromosome 19. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TCTGGGATGGGTGCTCAATAAGGCTGTGGTCTCTGGCATACCAGGAGAATGAGTCAAAGTTGGAACAGTTGTACTGGTTGCTGCCCCAGAACTAGTGATCTGTGAAGTCACCATCTCTGGTGCACCAGGTGAGATTGTTGTCAGTACAGCTGAACTGGCTTCTGTCCTAGGACTGGTGGCCATTACAGGTGTGGCATCTGGACTACTATGGGAAAAACTGGAGGTTGTTCTGGAAACAGGTGTGCTGGTCTGTGGAGGATGAGTGACCCAGGAAGCCATTGTATCTGGCTCACTAGAGGGAACAGTCCGAATTGGAACAG... | TCTGGGATGGGTGCTCAATAAGGCTGTGGTCTCTGGCATACCAGGAGAATGAGTCAAAGTTGGAACAGTTGTACTGGTTGCTGCCCCAGAACTAGTGATCTGTGAAGTCACCATCTCTGGTGCACCAGGTGAGATTGTTGTCAGTACAGCTGAACTGGCTTCTGTCCTAGGACTGGTGGCCATTACAGGTGTGGCATCTGGACTACTATGGGAAAAACTGGAGGTTGTTCTGGAAACAGGTGTGCTGGTCTGTGGAGGATGAGTGACCCAGGAAGCCATTGTATCTGGCTCACTAGAGGGAACAGTCCGAATTGGAACAG... |
Task1_train_46424 | This variant is located on Chromosome 19. Evaluate its biological effect and specify any disease association. | Benign | AAGTTGGGAATTGTCCCAGAAACCGTTGTGCTGGTTTCTGCAGGATGAGTGAGCCACGTGGCTGTAGTCTCTGGTTCATATGGGGTCTCACTCAATGTTGGGAAGGTTGTACTGGTGTCTGTCCCAGAACTAGGGACCAGTGAGGTCACCAGATCTGACATATCAGGTGAGATAGTTGTCGTTGAAACAGCTGAACTGGCTTCTGGCCCAGGACTGGTGATGGCTACTGGGAGTGTGGTGTCTGACTTACTATGGGAAAACTTGGGAGTTGTCCTGGGAACCATTGTGTTGGTCTCTGCAGGATGAATGAGCTGTATGGC... | AAGTTGGGAATTGTCCCAGAAACCGTTGTGCTGGTTTCTGCAGGATGAGTGAGCCACGTGGCTGTAGTCTCTGGTTCATATGGGGTCTCACTCAATGTTGGGAAGGTTGTACTGGTGTCTGTCCCAGAACTAGGGACCAGTGAGGTCACCAGATCTGACATATCAGGTGAGATAGTTGTCGTTGAAACAGCTGAACTGGCTTCTGGCCCAGGACTGGTGATGGCTACTGGGAGTGTGGTGTCTGACTTACTATGGGAAAACTTGGGAGTTGTCCTGGGAACCATTGTGTTGGTCTCTGCAGGATGAATGAGCTGTATGGC... |
Task1_train_46425 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GGAAAACTTGGGAGTTGTCCTGGGAACCATTGTGTTGGTCTCTGCAGGATGAATGAGCTGTATGGCTGTTGTCTCTGGTTCATATGGGGTCTCCGTCAGTGTTGGGAAAGTTGTAGTGCTGTCTGTCCCAGAACTGATGACCAGTGAGGTCAGCATCTTTGATGCACCAGGGGAGACAGGGAGAGTTGGAATGGCTGAACTTGTGTGTGTCTCAGAATAGGTGATAAATGAGGTTGTGGTCTCTGGCTCACCAGAAGAAAGAGTCAGAGTTGGAATAGTTATACTGGTGTCTGTCCCAGAACTAGTGACCTGTGAGGTTA... | GGAAAACTTGGGAGTTGTCCTGGGAACCATTGTGTTGGTCTCTGCAGGATGAATGAGCTGTATGGCTGTTGTCTCTGGTTCATATGGGGTCTCCGTCAGTGTTGGGAAAGTTGTAGTGCTGTCTGTCCCAGAACTGATGACCAGTGAGGTCAGCATCTTTGATGCACCAGGGGAGACAGGGAGAGTTGGAATGGCTGAACTTGTGTGTGTCTCAGAATAGGTGATAAATGAGGTTGTGGTCTCTGGCTCACCAGAAGAAAGAGTCAGAGTTGGAATAGTTATACTGGTGTCTGTCCCAGAACTAGTGACCTGTGAGGTTA... |
Task1_train_46426 | Mutation context: Chromosome 19. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | TGGAGACAGTCAAAGTTGGAACAACAGAACTTGCTTCTGTCCCAGGATGAGCGACCCATGAGTCTATGGTCTCTGGTTGACTTGAGGCAACAGTTAGATTTGAAAACGCACTGGTCTCTGACCCAGAACTAGTGACCAGTGAAGTCACCAGCCCTTGTACAGTAGGGGAGACAGCTAAAGTTGGAATGGCTGAAATCATCTTTGCCTCAGAATGGGTGACCAATGAAGTTGTGGTCTCTGGTTCATCAGAAGAAATAGTCAGAGTTGGAATAGTTGTACTGGTTACTGCTCTAGAACTAGTGACCAGAGAGGTCACCATT... | TGGAGACAGTCAAAGTTGGAACAACAGAACTTGCTTCTGTCCCAGGATGAGCGACCCATGAGTCTATGGTCTCTGGTTGACTTGAGGCAACAGTTAGATTTGAAAACGCACTGGTCTCTGACCCAGAACTAGTGACCAGTGAAGTCACCAGCCCTTGTACAGTAGGGGAGACAGCTAAAGTTGGAATGGCTGAAATCATCTTTGCCTCAGAATGGGTGACCAATGAAGTTGTGGTCTCTGGTTCATCAGAAGAAATAGTCAGAGTTGGAATAGTTGTACTGGTTACTGCTCTAGAACTAGTGACCAGAGAGGTCACCATT... |
Task1_train_46427 | Chromosome 19 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TTCCTTCCATTCACTCTTCTCTCCATTCTTCCTTTTATCCATCCAACTACACTTCTCCCTTCTCGCCATGCCATTCATCACTTGCTTACTGAACACCCGTGACTCAACTACTGAGTCACATAGTAACATATGGGTCAATAGCCACCAATGTGTCTAAATTTAGTGTGAATTACAAAATAATGTGAAGAAGGAGAGGGAGCAAATCATTCTCCTGGAGATATTGTCCAGTGAGGCAGAAACTCGAGTCGTTGGAGGGCCTCTTTGGATTTGTGTCCAGAACAAAAGTTGGTGCCAAGCTCAACCCTTTCAGAGGAATGGAA... | TTCCTTCCATTCACTCTTCTCTCCATTCTTCCTTTTATCCATCCAACTACACTTCTCCCTTCTCGCCATGCCATTCATCACTTGCTTACTGAACACCCGTGACTCAACTACTGAGTCACATAGTAACATATGGGTCAATAGCCACCAATGTGTCTAAATTTAGTGTGAATTACAAAATAATGTGAAGAAGGAGAGGGAGCAAATCATTCTCCTGGAGATATTGTCCAGTGAGGCAGAAACTCGAGTCGTTGGAGGGCCTCTTTGGATTTGTGTCCAGAACAAAAGTTGGTGCCAAGCTCAACCCTTTCAGAGGAATGGAA... |
Task1_train_46428 | This mutation is located on Chromosome 19. Is it associated with a disease or is it a benign polymorphism? | Benign | CATTCACTCTTCTCTCCATTCTTCCTTTTATCCATCCAACTACACTTCTCCCTTCTCGCCATGCCATTCATCACTTGCTTACTGAACACCCGTGACTCAACTACTGAGTCACATAGTAACATATGGGTCAATAGCCACCAATGTGTCTAAATTTAGTGTGAATTACAAAATAATGTGAAGAAGGAGAGGGAGCAAATCATTCTCCTGGAGATATTGTCCAGTGAGGCAGAAACTCGAGTCGTTGGAGGGCCTCTTTGGATTTGTGTCCAGAACAAAAGTTGGTGCCAAGCTCAACCCTTTCAGAGGAATGGAATCCCCAA... | CATTCACTCTTCTCTCCATTCTTCCTTTTATCCATCCAACTACACTTCTCCCTTCTCGCCATGCCATTCATCACTTGCTTACTGAACACCCGTGACTCAACTACTGAGTCACATAGTAACATATGGGTCAATAGCCACCAATGTGTCTAAATTTAGTGTGAATTACAAAATAATGTGAAGAAGGAGAGGGAGCAAATCATTCTCCTGGAGATATTGTCCAGTGAGGCAGAAACTCGAGTCGTTGGAGGGCCTCTTTGGATTTGTGTCCAGAACAAAAGTTGGTGCCAAGCTCAACCCTTTCAGAGGAATGGAATCCCCAA... |
Task1_train_46429 | An alteration has been detected on Chromosome 19. Is it pathogenic, and if so, what disease is involved? | Benign | CTTTTCTGTTACCTCTCTGACCACTCCTGTTTAGCCCAGCAGTTAGGAGCATGAGTTCCTAGTGACACACAATTTGAGTTCTTATCCTAGTTCTATTGCTTTCTAGCTATATGGACTTAAGAAAGTTACTTAATCTCCCTGTGCCTAAATGTCTTCATCTCCAAAATAGGCTTCTAATAATCTCTACTTCAATTAGTGTTACAATTGAGGATCAAATAGCTTAATAAAACTGCACTTGAAACAGAGTAAGTACTGTTATAAATATTTTCTGTTGTCATTCTTATTGTCATCATCATCATTACTAGTAGTAATATTAGAGC... | CTTTTCTGTTACCTCTCTGACCACTCCTGTTTAGCCCAGCAGTTAGGAGCATGAGTTCCTAGTGACACACAATTTGAGTTCTTATCCTAGTTCTATTGCTTTCTAGCTATATGGACTTAAGAAAGTTACTTAATCTCCCTGTGCCTAAATGTCTTCATCTCCAAAATAGGCTTCTAATAATCTCTACTTCAATTAGTGTTACAATTGAGGATCAAATAGCTTAATAAAACTGCACTTGAAACAGAGTAAGTACTGTTATAAATATTTTCTGTTGTCATTCTTATTGTCATCATCATCATTACTAGTAGTAATATTAGAGC... |
Task1_train_46430 | This variant is found on Chromosome 19. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GACACACAATTTGAGTTCTTATCCTAGTTCTATTGCTTTCTAGCTATATGGACTTAAGAAAGTTACTTAATCTCCCTGTGCCTAAATGTCTTCATCTCCAAAATAGGCTTCTAATAATCTCTACTTCAATTAGTGTTACAATTGAGGATCAAATAGCTTAATAAAACTGCACTTGAAACAGAGTAAGTACTGTTATAAATATTTTCTGTTGTCATTCTTATTGTCATCATCATCATTACTAGTAGTAATATTAGAGCACCTATCACGATACTGTAATGATTCAATTATTTGCTTATTTTTGTTTCTCCAATTCCTTAACC... | GACACACAATTTGAGTTCTTATCCTAGTTCTATTGCTTTCTAGCTATATGGACTTAAGAAAGTTACTTAATCTCCCTGTGCCTAAATGTCTTCATCTCCAAAATAGGCTTCTAATAATCTCTACTTCAATTAGTGTTACAATTGAGGATCAAATAGCTTAATAAAACTGCACTTGAAACAGAGTAAGTACTGTTATAAATATTTTCTGTTGTCATTCTTATTGTCATCATCATCATTACTAGTAGTAATATTAGAGCACCTATCACGATACTGTAATGATTCAATTATTTGCTTATTTTTGTTTCTCCAATTCCTTAACC... |
Task1_train_46431 | A change on Chromosome 19 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GGCAAATGAAGTCATGGCCTCTGATAGAGAAGGCATCACTGTGCCAGTGGAAATAGTCTCAGCTGAAGGCAGCAAATCTGTACTCAGATGATGAGTACTTTCTGTTACAGACATAGTAAACCTGGATTCTGGGAAGGAGGTTATCCCAGTGGACTCCGTAATAGATGGAGAAGCATTAAAGGGGGTGATTATGTCCACTGGAATTTCAGTATACTGTGAGGCTGGAGGCCAGTCTGGGGATGATGTTTTTGCAGAAGAGGTGAAATCAGTCTTGGAACTCTGTAAAAGGTGAGTGGACCCAGGAGAAGAAGGTGTATTTG... | GGCAAATGAAGTCATGGCCTCTGATAGAGAAGGCATCACTGTGCCAGTGGAAATAGTCTCAGCTGAAGGCAGCAAATCTGTACTCAGATGATGAGTACTTTCTGTTACAGACATAGTAAACCTGGATTCTGGGAAGGAGGTTATCCCAGTGGACTCCGTAATAGATGGAGAAGCATTAAAGGGGGTGATTATGTCCACTGGAATTTCAGTATACTGTGAGGCTGGAGGCCAGTCTGGGGATGATGTTTTTGCAGAAGAGGTGAAATCAGTCTTGGAACTCTGTAAAAGGTGAGTGGACCCAGGAGAAGAAGGTGTATTTG... |
Task1_train_46432 | This mutation occurs on Chromosome 19. Does this change lead to a known medical condition, or is it benign? | Benign | AAAAGGTGAGTGGACCCAGGAGAAGAAGGTGTATTTGTTGGTGTGACTGAGCTGGTGTCCAGGGACATGTTTGTCTTCCTAAATCCAGAAGTCAAATGAGAAAATGGCTCAGCCTCAAATCCTGTGGTCTCAAAATTAGCAGGCATTGATGTGGAAATAGAGGTTTCAGCCATGGAAGAGGGAGTACCCACTGGGTATGTAGCCTTGGATGGCTCCGAGTGGATTGAAACAGAGGAATATAGTTCATGTCCAGAACTGGTGGTTCCCACATTGGTCACTGCCATGCTTGAAGAAGGATGAATTTTCTCTGTATCTGTGGT... | AAAAGGTGAGTGGACCCAGGAGAAGAAGGTGTATTTGTTGGTGTGACTGAGCTGGTGTCCAGGGACATGTTTGTCTTCCTAAATCCAGAAGTCAAATGAGAAAATGGCTCAGCCTCAAATCCTGTGGTCTCAAAATTAGCAGGCATTGATGTGGAAATAGAGGTTTCAGCCATGGAAGAGGGAGTACCCACTGGGTATGTAGCCTTGGATGGCTCCGAGTGGATTGAAACAGAGGAATATAGTTCATGTCCAGAACTGGTGGTTCCCACATTGGTCACTGCCATGCTTGAAGAAGGATGAATTTTCTCTGTATCTGTGGT... |
Task1_train_46433 | A mutation found on Chromosome 19 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | TGTTGGTGTGACTGAGCTGGTGTCCAGGGACATGTTTGTCTTCCTAAATCCAGAAGTCAAATGAGAAAATGGCTCAGCCTCAAATCCTGTGGTCTCAAAATTAGCAGGCATTGATGTGGAAATAGAGGTTTCAGCCATGGAAGAGGGAGTACCCACTGGGTATGTAGCCTTGGATGGCTCCGAGTGGATTGAAACAGAGGAATATAGTTCATGTCCAGAACTGGTGGTTCCCACATTGGTCACTGCCATGCTTGAAGAAGGATGAATTTTCTCTGTATCTGTGGTGACTTCAGAGGCAGCCAGTATTTCAACTGAGGTGC... | TGTTGGTGTGACTGAGCTGGTGTCCAGGGACATGTTTGTCTTCCTAAATCCAGAAGTCAAATGAGAAAATGGCTCAGCCTCAAATCCTGTGGTCTCAAAATTAGCAGGCATTGATGTGGAAATAGAGGTTTCAGCCATGGAAGAGGGAGTACCCACTGGGTATGTAGCCTTGGATGGCTCCGAGTGGATTGAAACAGAGGAATATAGTTCATGTCCAGAACTGGTGGTTCCCACATTGGTCACTGCCATGCTTGAAGAAGGATGAATTTTCTCTGTATCTGTGGTGACTTCAGAGGCAGCCAGTATTTCAACTGAGGTGC... |
Task1_train_46434 | Assess the clinical impact of this variant found on Chromosome 19. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GAACTGGTGGTTCCCACATTGGTCACTGCCATGCTTGAAGAAGGATGAATTTTCTCTGTATCTGTGGTGACTTCAGAGGCAGCCAGTATTTCAACTGAGGTGCCACTCAGATTTGGAGATAAACTGGTTCCAGGTTCTGTGCTTGTGTCTGTAGTCTTCACCATGCCTGGGGTGAGGAGTGAAGTCACAGAAAAAGAGGAGGAAGGGATACTCTGCGGTAATGTGGAAGAAACAGAAGGTGAGGTCGTGACAGGTAAGGACAACAGAGAAGATGAAGAGCTAGTTTTTTCCACAAAGAGAGAGCTCTTCCATGATGGATT... | GAACTGGTGGTTCCCACATTGGTCACTGCCATGCTTGAAGAAGGATGAATTTTCTCTGTATCTGTGGTGACTTCAGAGGCAGCCAGTATTTCAACTGAGGTGCCACTCAGATTTGGAGATAAACTGGTTCCAGGTTCTGTGCTTGTGTCTGTAGTCTTCACCATGCCTGGGGTGAGGAGTGAAGTCACAGAAAAAGAGGAGGAAGGGATACTCTGCGGTAATGTGGAAGAAACAGAAGGTGAGGTCGTGACAGGTAAGGACAACAGAGAAGATGAAGAGCTAGTTTTTTCCACAAAGAGAGAGCTCTTCCATGATGGATT... |
Task1_train_46435 | Here is a genetic alteration on Chromosome 19. Based on the data, is it a benign variant or a cause of disease? | Benign | CAGAGGCAGCCAGTATTTCAACTGAGGTGCCACTCAGATTTGGAGATAAACTGGTTCCAGGTTCTGTGCTTGTGTCTGTAGTCTTCACCATGCCTGGGGTGAGGAGTGAAGTCACAGAAAAAGAGGAGGAAGGGATACTCTGCGGTAATGTGGAAGAAACAGAAGGTGAGGTCGTGACAGGTAAGGACAACAGAGAAGATGAAGAGCTAGTTTTTTCCACAAAGAGAGAGCTCTTCCATGATGGATTTTCAGGACTCCTACTCATAAGAGTTGTCATCTCTGAGTGTAAAAATCTAGGAGGAACAGTTGAGTGGGTCCTT... | CAGAGGCAGCCAGTATTTCAACTGAGGTGCCACTCAGATTTGGAGATAAACTGGTTCCAGGTTCTGTGCTTGTGTCTGTAGTCTTCACCATGCCTGGGGTGAGGAGTGAAGTCACAGAAAAAGAGGAGGAAGGGATACTCTGCGGTAATGTGGAAGAAACAGAAGGTGAGGTCGTGACAGGTAAGGACAACAGAGAAGATGAAGAGCTAGTTTTTTCCACAAAGAGAGAGCTCTTCCATGATGGATTTTCAGGACTCCTACTCATAAGAGTTGTCATCTCTGAGTGTAAAAATCTAGGAGGAACAGTTGAGTGGGTCCTT... |
Task1_train_46436 | A genomic change on Chromosome 19 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CACTTGTTTCTGTGATTGAGGTGGTCTCTTCAGAGGTGCTAGTCTCCCTGAATCCAGGAGTCAATGAGAATGTTGGCTCTGTCGGAATCCTCCTAGTCTCAGAGAAGGCAGGATTTGATGTGAAAACAGTGGTATCGTCCACAGCGGAGGTGATACCCATTGAAGGTATGGTTATGGTTGTTTCTGAGTCAGCTAGGACAGAGGAATGAGATTCATGAACAGAACTGGAGGTCCTCACTTTGGCCACCGCTGTGTTTGAGGAAGGATGAATTTTCTCTGTATCTGTCATGATTTCAGAGGTGGCCGGTATTTCAACTGAG... | CACTTGTTTCTGTGATTGAGGTGGTCTCTTCAGAGGTGCTAGTCTCCCTGAATCCAGGAGTCAATGAGAATGTTGGCTCTGTCGGAATCCTCCTAGTCTCAGAGAAGGCAGGATTTGATGTGAAAACAGTGGTATCGTCCACAGCGGAGGTGATACCCATTGAAGGTATGGTTATGGTTGTTTCTGAGTCAGCTAGGACAGAGGAATGAGATTCATGAACAGAACTGGAGGTCCTCACTTTGGCCACCGCTGTGTTTGAGGAAGGATGAATTTTCTCTGTATCTGTCATGATTTCAGAGGTGGCCGGTATTTCAACTGAG... |
Task1_train_46437 | A mutation on Chromosome 19 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GTGTTTGAGGAAGGATGAATTTTCTCTGTATCTGTCATGATTTCAGAGGTGGCCGGTATTTCAACTGAGGTGCTGCTCAAATTTGGAGATGAACTGGTTTTAGGCTCTGAGCTTGTATCCAACACTTCTGTAGTCTTCACCAGGCCTGGGAGGATAAGTGAAGTCACAGGAAGAGGAGAGGAGGGGCTACTGTCTAGTAATGTGGAGGACACAGGAGAAAGTGAGGTCGTGAGAGGTAATGATGTCAGAGAAGAGGAAGATCTAGTTGTTTCCACAAAGCGAGGGCTCGTCCATGACAGACTTTCAGGACCCCTGCTCAT... | GTGTTTGAGGAAGGATGAATTTTCTCTGTATCTGTCATGATTTCAGAGGTGGCCGGTATTTCAACTGAGGTGCTGCTCAAATTTGGAGATGAACTGGTTTTAGGCTCTGAGCTTGTATCCAACACTTCTGTAGTCTTCACCAGGCCTGGGAGGATAAGTGAAGTCACAGGAAGAGGAGAGGAGGGGCTACTGTCTAGTAATGTGGAGGACACAGGAGAAAGTGAGGTCGTGAGAGGTAATGATGTCAGAGAAGAGGAAGATCTAGTTGTTTCCACAAAGCGAGGGCTCGTCCATGACAGACTTTCAGGACCCCTGCTCAT... |
Task1_train_46438 | This variant is present on Chromosome 19. Is the change likely to result in a pathogenic outcome? | Benign | TGTATCTGTCATGATTTCAGAGGTGGCCGGTATTTCAACTGAGGTGCTGCTCAAATTTGGAGATGAACTGGTTTTAGGCTCTGAGCTTGTATCCAACACTTCTGTAGTCTTCACCAGGCCTGGGAGGATAAGTGAAGTCACAGGAAGAGGAGAGGAGGGGCTACTGTCTAGTAATGTGGAGGACACAGGAGAAAGTGAGGTCGTGAGAGGTAATGATGTCAGAGAAGAGGAAGATCTAGTTGTTTCCACAAAGCGAGGGCTCGTCCATGACAGACTTTCAGGACCCCTGCTCATAAGATTGGTCATCTCTGAGTGTGAAA... | TGTATCTGTCATGATTTCAGAGGTGGCCGGTATTTCAACTGAGGTGCTGCTCAAATTTGGAGATGAACTGGTTTTAGGCTCTGAGCTTGTATCCAACACTTCTGTAGTCTTCACCAGGCCTGGGAGGATAAGTGAAGTCACAGGAAGAGGAGAGGAGGGGCTACTGTCTAGTAATGTGGAGGACACAGGAGAAAGTGAGGTCGTGAGAGGTAATGATGTCAGAGAAGAGGAAGATCTAGTTGTTTCCACAAAGCGAGGGCTCGTCCATGACAGACTTTCAGGACCCCTGCTCATAAGATTGGTCATCTCTGAGTGTGAAA... |
Task1_train_46439 | This alteration occurs on Chromosome 19. Is it associated with a disease or is it a benign variant? | Benign | AGAGGTAGACAGCCTGGTGACAACTTCATCGGAGATGTCTAGTGACATTGTGGACTGAGCAGGGCCAGGAATGGATGTTCTGCTAGAGGGCATAACTTCTGTCCTGGAGACCTCAGGAGTGGCACCAGAGGGCATCTTGTAAAGGACAGTGCTTGTCTCTGTGGATGAGGTGATGTCCTGGGAGGTTCTGGTCTCCCTCAGTCCAGGGGTCAGAGATGACATTGACTCTATCTCAATCCTTGTAATGCCAGAGGAGCCAGGCATTGTTGTGGAAACCATGTTGTCTCTTATAGAGGAAGAGGTGACCACTGGAGATATCA... | AGAGGTAGACAGCCTGGTGACAACTTCATCGGAGATGTCTAGTGACATTGTGGACTGAGCAGGGCCAGGAATGGATGTTCTGCTAGAGGGCATAACTTCTGTCCTGGAGACCTCAGGAGTGGCACCAGAGGGCATCTTGTAAAGGACAGTGCTTGTCTCTGTGGATGAGGTGATGTCCTGGGAGGTTCTGGTCTCCCTCAGTCCAGGGGTCAGAGATGACATTGACTCTATCTCAATCCTTGTAATGCCAGAGGAGCCAGGCATTGTTGTGGAAACCATGTTGTCTCTTATAGAGGAAGAGGTGACCACTGGAGATATCA... |
Task1_train_46440 | Consider a variant on Chromosome 19. Determine its clinical classification and disease relevance. | Benign | GTGCCTTGTAAGGAACAGTGCTTGGCTTTGTGGCTGAGTGGATCTCCTGGGAGGTGCTGGTCTCCCTTGGTGTGGGGGTCAGGGTGGATGTTGACTCCATCTCAATTCTTGTTATCTCAGAGGAAGCAGGTATGGTTGTAGAAACAATGTCTTTTATGGTGGAAGAGGTGACCACTGGAGATGTCACTTTGGATGGCTCTGGGAGGCCTGGATAAGAGGAATAGAATTCTTGTCTAGCGCTGATGGTGCCCATCTGAGTCACAGCTGTGTTTTCTGAAAGCTGAATTGCCTCTGTCTCCATGGTGGCTTTAGAAGTGGCC... | GTGCCTTGTAAGGAACAGTGCTTGGCTTTGTGGCTGAGTGGATCTCCTGGGAGGTGCTGGTCTCCCTTGGTGTGGGGGTCAGGGTGGATGTTGACTCCATCTCAATTCTTGTTATCTCAGAGGAAGCAGGTATGGTTGTAGAAACAATGTCTTTTATGGTGGAAGAGGTGACCACTGGAGATGTCACTTTGGATGGCTCTGGGAGGCCTGGATAAGAGGAATAGAATTCTTGTCTAGCGCTGATGGTGCCCATCTGAGTCACAGCTGTGTTTTCTGAAAGCTGAATTGCCTCTGTCTCCATGGTGGCTTTAGAAGTGGCC... |
Task1_train_46441 | This mutation occurs on Chromosome 19. Does this change lead to a known medical condition, or is it benign? | Benign | ACTCGTATCCTCCATGGTGGAGGTAATAACCATTGGAGATGTGACTTTGGATGTCTGTGAGTCAGCTAGGACAAAGGAAGTGGATTCATGTCCAGAACTGGAGGTCCCCACATCGGTCACTGTTCTGTTTGAAGAAGGATGAGTTTTCTCTGTATCTGTGGTGACTTCAGAGGTGGCCAGTATTTCAACTGAGGTGCTGCTCAAATTTGCAGGTGAGTTGGTTACAGGTTCTGAGCTTTTGTGCAACATATCTGTAGTTTTTGCCAAGCCAGACGTGAGGAGTGAAGTCACAGGAAGAGGAGAGGAAGAGATGCTCTCTG... | ACTCGTATCCTCCATGGTGGAGGTAATAACCATTGGAGATGTGACTTTGGATGTCTGTGAGTCAGCTAGGACAAAGGAAGTGGATTCATGTCCAGAACTGGAGGTCCCCACATCGGTCACTGTTCTGTTTGAAGAAGGATGAGTTTTCTCTGTATCTGTGGTGACTTCAGAGGTGGCCAGTATTTCAACTGAGGTGCTGCTCAAATTTGCAGGTGAGTTGGTTACAGGTTCTGAGCTTTTGTGCAACATATCTGTAGTTTTTGCCAAGCCAGACGTGAGGAGTGAAGTCACAGGAAGAGGAGAGGAAGAGATGCTCTCTG... |
Task1_train_46442 | Consider a variant on Chromosome 19. Determine its clinical classification and disease relevance. | Benign | AGGACCCCTCCTCATAAGAGTGCTCATCTGTGAGTGTGAAAATCCTTGAGATATAGTTGAGTGTGTCATTGTCAAAGAGGTTGTGCTTGACGTGTCCAAAGTACTGGTGCCTTGTGTTGTGGCCCCTAAAGGACTTGTATGGGTGTTCATGGTTATTTCTGCTGATTCTGTCATGACAGGGGATGTAGAGAACCAGCTGACGGTTCTTGTGGAGATGTCTGGTGATATTGTGGATTGAGCGGGACCTGGGATGGAGGTGACGTCTTCCTTGGAGATCTCAGTAGTAGCACCAGTGGGCACTTTAGAGAGGACAGTGCTCA... | AGGACCCCTCCTCATAAGAGTGCTCATCTGTGAGTGTGAAAATCCTTGAGATATAGTTGAGTGTGTCATTGTCAAAGAGGTTGTGCTTGACGTGTCCAAAGTACTGGTGCCTTGTGTTGTGGCCCCTAAAGGACTTGTATGGGTGTTCATGGTTATTTCTGCTGATTCTGTCATGACAGGGGATGTAGAGAACCAGCTGACGGTTCTTGTGGAGATGTCTGGTGATATTGTGGATTGAGCGGGACCTGGGATGGAGGTGACGTCTTCCTTGGAGATCTCAGTAGTAGCACCAGTGGGCACTTTAGAGAGGACAGTGCTCA... |
Task1_train_46443 | A mutation on Chromosome 19 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | CAGTGAGGAAGCTGGCTCTGACTGAATTTTCCTAGTGTTAGATAAGGCAGGAGTTAATGTAGAAACACTTGTATCCCCCATAATGGAGATGGTACCCATTGCCGATGTGGCTTTGGTTGTCTCTGAGTCAGGTAGGACAGAGGAAGGGGATTCATGTCCAGAACTGGAAGTTCCAACTTTGGTTACTGCCGTGTTTGAGAAAGGATGAATTTTCTCCGTATCTGTGGTGACTTCAGAGGTGGCCAGTATTTCAACTGAGGTGCTGCTCAAACTTGGAGGTGAACTGGTTTCAGGTTCTGCACTTGCGTCCAACACCTCAG... | CAGTGAGGAAGCTGGCTCTGACTGAATTTTCCTAGTGTTAGATAAGGCAGGAGTTAATGTAGAAACACTTGTATCCCCCATAATGGAGATGGTACCCATTGCCGATGTGGCTTTGGTTGTCTCTGAGTCAGGTAGGACAGAGGAAGGGGATTCATGTCCAGAACTGGAAGTTCCAACTTTGGTTACTGCCGTGTTTGAGAAAGGATGAATTTTCTCCGTATCTGTGGTGACTTCAGAGGTGGCCAGTATTTCAACTGAGGTGCTGCTCAAACTTGGAGGTGAACTGGTTTCAGGTTCTGCACTTGCGTCCAACACCTCAG... |
Task1_train_46444 | A mutation on Chromosome 19 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | TGCCCAAGTTTGGAGGTAAACTGGCCACAGATGCCAGCATATCTGTGGTCTTCACTAGGCCAGAGGTGGGGAGTGAAGTCAGATGAACAGGAGAAGACGGCCTACTTTCTGGTAATGTAGTAGGTACAGGGGACGGTGAGGTTATTGCTGGTAAAGACAGAAGGGAAGAGGAAGAGCTGGTTTTTTCCACAGAGGGTGGGCTTGTCCCTGATATGTACTCAGGAACTCTACTCGTAAGAGTGGACAAATCTAATTGTGAAAATCCATGAGTCATAGCTGAGTGGGTCCCTGCCTGTGAGGTTGTGATTGATGTGTCCCAG... | TGCCCAAGTTTGGAGGTAAACTGGCCACAGATGCCAGCATATCTGTGGTCTTCACTAGGCCAGAGGTGGGGAGTGAAGTCAGATGAACAGGAGAAGACGGCCTACTTTCTGGTAATGTAGTAGGTACAGGGGACGGTGAGGTTATTGCTGGTAAAGACAGAAGGGAAGAGGAAGAGCTGGTTTTTTCCACAGAGGGTGGGCTTGTCCCTGATATGTACTCAGGAACTCTACTCGTAAGAGTGGACAAATCTAATTGTGAAAATCCATGAGTCATAGCTGAGTGGGTCCCTGCCTGTGAGGTTGTGATTGATGTGTCCCAG... |
Task1_train_46445 | A variant was discovered on Chromosome 19. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CCTACTTTCTGGTAATGTAGTAGGTACAGGGGACGGTGAGGTTATTGCTGGTAAAGACAGAAGGGAAGAGGAAGAGCTGGTTTTTTCCACAGAGGGTGGGCTTGTCCCTGATATGTACTCAGGAACTCTACTCGTAAGAGTGGACAAATCTAATTGTGAAAATCCATGAGTCATAGCTGAGTGGGTCCCTGCCTGTGAGGTTGTGATTGATGTGTCCCAGGTAAGGGTACCCTGTGATGTCGCCCTATGAGGACCTGTTTGGGTGGCAATGGTCCTTTCTTCGGATTTTGTCAGGCCAGCAAAAGTAGAAAGCATGGTGA... | CCTACTTTCTGGTAATGTAGTAGGTACAGGGGACGGTGAGGTTATTGCTGGTAAAGACAGAAGGGAAGAGGAAGAGCTGGTTTTTTCCACAGAGGGTGGGCTTGTCCCTGATATGTACTCAGGAACTCTACTCGTAAGAGTGGACAAATCTAATTGTGAAAATCCATGAGTCATAGCTGAGTGGGTCCCTGCCTGTGAGGTTGTGATTGATGTGTCCCAGGTAAGGGTACCCTGTGATGTCGCCCTATGAGGACCTGTTTGGGTGGCAATGGTCCTTTCTTCGGATTTTGTCAGGCCAGCAAAAGTAGAAAGCATGGTGA... |
Task1_train_46446 | Given this context: Chromosome 19 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AAGTAGAAAGCATGGTGACAGATCTTGTGGAGGTGTCCGGTGACATTGTGGGCTTTTCAGTGCCTTGGATGGATGTTCTGCTAGAGGAGGTGAGTTCTGTTCTGGAGACCTCAGTAGTAGCAGCAGTGAATGCTTTGTCAAAGACCGTGCTTGTGTCTGAGGATGAGCCAATTTTCTGGGAGGTGCTAGTCTCCCTCAGTCTAAATATCAGGGAGAAAGTTGTCTCAGACTCAATCTTTTTCATCGCAGAGGATCTAGGCATTGATGTGGAAACTATTGAGTCCCCCGAGGTGGAAGTGATAACTACTGCGGATGTGGCT... | AAGTAGAAAGCATGGTGACAGATCTTGTGGAGGTGTCCGGTGACATTGTGGGCTTTTCAGTGCCTTGGATGGATGTTCTGCTAGAGGAGGTGAGTTCTGTTCTGGAGACCTCAGTAGTAGCAGCAGTGAATGCTTTGTCAAAGACCGTGCTTGTGTCTGAGGATGAGCCAATTTTCTGGGAGGTGCTAGTCTCCCTCAGTCTAAATATCAGGGAGAAAGTTGTCTCAGACTCAATCTTTTTCATCGCAGAGGATCTAGGCATTGATGTGGAAACTATTGAGTCCCCCGAGGTGGAAGTGATAACTACTGCGGATGTGGCT... |
Task1_train_46447 | This variant is present on Chromosome 19. Is the change likely to result in a pathogenic outcome? | Benign | GGTGTCCGGTGACATTGTGGGCTTTTCAGTGCCTTGGATGGATGTTCTGCTAGAGGAGGTGAGTTCTGTTCTGGAGACCTCAGTAGTAGCAGCAGTGAATGCTTTGTCAAAGACCGTGCTTGTGTCTGAGGATGAGCCAATTTTCTGGGAGGTGCTAGTCTCCCTCAGTCTAAATATCAGGGAGAAAGTTGTCTCAGACTCAATCTTTTTCATCGCAGAGGATCTAGGCATTGATGTGGAAACTATTGAGTCCCCCGAGGTGGAAGTGATAACTACTGCGGATGTGGCTTTATATGGGTCTGAGTCAGGTGAGACAGTAA... | GGTGTCCGGTGACATTGTGGGCTTTTCAGTGCCTTGGATGGATGTTCTGCTAGAGGAGGTGAGTTCTGTTCTGGAGACCTCAGTAGTAGCAGCAGTGAATGCTTTGTCAAAGACCGTGCTTGTGTCTGAGGATGAGCCAATTTTCTGGGAGGTGCTAGTCTCCCTCAGTCTAAATATCAGGGAGAAAGTTGTCTCAGACTCAATCTTTTTCATCGCAGAGGATCTAGGCATTGATGTGGAAACTATTGAGTCCCCCGAGGTGGAAGTGATAACTACTGCGGATGTGGCTTTATATGGGTCTGAGTCAGGTGAGACAGTAA... |
Task1_train_46448 | A variant on Chromosome 19 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GTTGGCTTCTTCTGCAGAGAAAGGGCTTGTCTTCAACACATCATTGAGATCATTGTTCATGACACTGGTTGTTTCTGAATCTACAAAATCCTGAGTTCTGGCTGATGGAGTTCCTGCTGAGGTGGCTATGGTTGATGTGTCCAGGGTCAGTTGGCCAAGAGATGTCACCCCAGAAGGACCTGTTTGTGTGGCGATGGTCTTGTGTGTAGATATTGTCAAGGGAGGAGAGTTAGAATGACTGCTGCTGGCTTCAGGTGAAATGTCTGGGGACTTTGTTGACTGAGCAGAAGCTGGCATGAATGTAGGATCATAGTAGGTGA... | GTTGGCTTCTTCTGCAGAGAAAGGGCTTGTCTTCAACACATCATTGAGATCATTGTTCATGACACTGGTTGTTTCTGAATCTACAAAATCCTGAGTTCTGGCTGATGGAGTTCCTGCTGAGGTGGCTATGGTTGATGTGTCCAGGGTCAGTTGGCCAAGAGATGTCACCCCAGAAGGACCTGTTTGTGTGGCGATGGTCTTGTGTGTAGATATTGTCAAGGGAGGAGAGTTAGAATGACTGCTGCTGGCTTCAGGTGAAATGTCTGGGGACTTTGTTGACTGAGCAGAAGCTGGCATGAATGTAGGATCATAGTAGGTGA... |
Task1_train_46449 | This genomic variant is located on Chromosome 19. Can you determine its pathogenicity and name any linked disease? | Benign | AATGGAGGTCCCCACGTTGGCCACTGCAGTGTTTGTATGCATGGAAGCATGCATGGCTTCTGTGTGCGCAGTGTCTTTGTAAGTGGTCAGTCTCTCCTGTGTGGGGCTGCTTAAATTTGGAGGTGAACTCGTTACGGGCTCTGGGCTTGTTGTGCCCAATACATTTGTGGTTGTCACCAGAACAGAAGTAAGAAGTGCAGTCACAGGGAGAGGAGAGGAGGGGATGCTCTCTGGTGATGTGGAGGAAACAGGAGAAGGGGATGTCATGGAAGGTGACATCAGGGAAAACCCAGAGCTGGTTTCTTCCACAGGGGGAGTTG... | AATGGAGGTCCCCACGTTGGCCACTGCAGTGTTTGTATGCATGGAAGCATGCATGGCTTCTGTGTGCGCAGTGTCTTTGTAAGTGGTCAGTCTCTCCTGTGTGGGGCTGCTTAAATTTGGAGGTGAACTCGTTACGGGCTCTGGGCTTGTTGTGCCCAATACATTTGTGGTTGTCACCAGAACAGAAGTAAGAAGTGCAGTCACAGGGAGAGGAGAGGAGGGGATGCTCTCTGGTGATGTGGAGGAAACAGGAGAAGGGGATGTCATGGAAGGTGACATCAGGGAAAACCCAGAGCTGGTTTCTTCCACAGGGGGAGTTG... |
Task1_train_46450 | A change on Chromosome 19 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TGTGTCCCAGGGAAGGATACCCTGTGATGTAGCCCCAGGAGTAGTTGTTTGAGTGGTGACGGTCATTTCTGCAGATTTTGTCATGATGGGGGAGGTGAAGAGCCTGGTGATCATTCCTGTGGAGATGTCGGGTGCTATTGTGGGCCGATCAAGGTCTGAGATGGATGTTCTGCTAGAGGAGATTTCTGTTCTGGAGGCCTGAGTAATAGCACCTGTGGGCACATAAGAAAAGGCAGTATTTGTCTCTGTTGTTGAGCTGGTCTTCTCAGACGTGCTGCTCTCCCTCAGTCTAGGGCTCAGGGATGCTGTTGGCTCTGTTT... | TGTGTCCCAGGGAAGGATACCCTGTGATGTAGCCCCAGGAGTAGTTGTTTGAGTGGTGACGGTCATTTCTGCAGATTTTGTCATGATGGGGGAGGTGAAGAGCCTGGTGATCATTCCTGTGGAGATGTCGGGTGCTATTGTGGGCCGATCAAGGTCTGAGATGGATGTTCTGCTAGAGGAGATTTCTGTTCTGGAGGCCTGAGTAATAGCACCTGTGGGCACATAAGAAAAGGCAGTATTTGTCTCTGTTGTTGAGCTGGTCTTCTCAGACGTGCTGCTCTCCCTCAGTCTAGGGCTCAGGGATGCTGTTGGCTCTGTTT... |
Task1_train_46451 | This sequence variant lies on Chromosome 19. Is it clinically significant, and what condition might it cause if any? | Benign | CAGTATTTGTCTCTGTTGTTGAGCTGGTCTTCTCAGACGTGCTGCTCTCCCTCAGTCTAGGGCTCAGGGATGCTGTTGGCTCTGTTTGAATTTGGTTAGTCTGAGAGATATTAGGAGTTGATGTGGAAACACTTGTGTCCCCCAGGGTGGAGGTGGTACTCATCAGAGGTGTGGCTTTCGATGTCTCTGAGTCAGCTAGGACAGAGGATTGTGATTTATGTCCAGACCCGGAAGTCCCTACATTGGTCACTGCGGTGTTTGTGGAATGATGCATGGCGGCTTCTGTGTGTGCAGTGTCTTTGTAAGTGGCCGGTCTCTCA... | CAGTATTTGTCTCTGTTGTTGAGCTGGTCTTCTCAGACGTGCTGCTCTCCCTCAGTCTAGGGCTCAGGGATGCTGTTGGCTCTGTTTGAATTTGGTTAGTCTGAGAGATATTAGGAGTTGATGTGGAAACACTTGTGTCCCCCAGGGTGGAGGTGGTACTCATCAGAGGTGTGGCTTTCGATGTCTCTGAGTCAGCTAGGACAGAGGATTGTGATTTATGTCCAGACCCGGAAGTCCCTACATTGGTCACTGCGGTGTTTGTGGAATGATGCATGGCGGCTTCTGTGTGTGCAGTGTCTTTGTAAGTGGCCGGTCTCTCA... |
Task1_train_46452 | A change on Chromosome 19 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CAGGGGAATGGGATTCATGTCCAGAGTTGTTGGCTTTCACATTGGTCTCTTCTGTGTTTATAGAAGGAAAAATTTCCTTTGTGTCTTTACTGTCTTTAGAAGTGGCCAGTATCTTATCTGAGGTGCTGCTGAAATTTGGAAGTGAGCTGGTCACAGGTTCCAAGCGTGTACGTAATATGTCTGTAATCTTCACTAGGCCAGAGGTGAGAAGTGAAGTCATAGGAGAGGAGAGCTTATCCTCTGGTAAGGTAGAAGAAATCAGGGAAGGTGTGGTCATTGCAGGTGAGGACAGAAAGGAAGAGGGGGAGCTGGTTTTATCC... | CAGGGGAATGGGATTCATGTCCAGAGTTGTTGGCTTTCACATTGGTCTCTTCTGTGTTTATAGAAGGAAAAATTTCCTTTGTGTCTTTACTGTCTTTAGAAGTGGCCAGTATCTTATCTGAGGTGCTGCTGAAATTTGGAAGTGAGCTGGTCACAGGTTCCAAGCGTGTACGTAATATGTCTGTAATCTTCACTAGGCCAGAGGTGAGAAGTGAAGTCATAGGAGAGGAGAGCTTATCCTCTGGTAAGGTAGAAGAAATCAGGGAAGGTGTGGTCATTGCAGGTGAGGACAGAAAGGAAGAGGGGGAGCTGGTTTTATCC... |
Task1_train_46453 | A mutation is present on Chromosome 19. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CTAGGCCAGAGGTGAGAAGTGAAGTCATAGGAGAGGAGAGCTTATCCTCTGGTAAGGTAGAAGAAATCAGGGAAGGTGTGGTCATTGCAGGTGAGGACAGAAAGGAAGAGGGGGAGCTGGTTTTATCCACAGAGGGAGGACTTGTCCATGATACATCCTGTGGAATTCTGCTCATAAGAGTGGTCACATCCAATTGTGAAAATCCATGAGTCATAGCTGAGTGGATCCCTGCCTGGGGGGTTGTATTTGATGGGTCCATGGTAAAAGTATCCTGTGATGTAGCCCCATGAGGACCTGTTTGGGTGGTGATGGTTATTTCT... | CTAGGCCAGAGGTGAGAAGTGAAGTCATAGGAGAGGAGAGCTTATCCTCTGGTAAGGTAGAAGAAATCAGGGAAGGTGTGGTCATTGCAGGTGAGGACAGAAAGGAAGAGGGGGAGCTGGTTTTATCCACAGAGGGAGGACTTGTCCATGATACATCCTGTGGAATTCTGCTCATAAGAGTGGTCACATCCAATTGTGAAAATCCATGAGTCATAGCTGAGTGGATCCCTGCCTGGGGGGTTGTATTTGATGGGTCCATGGTAAAAGTATCCTGTGATGTAGCCCCATGAGGACCTGTTTGGGTGGTGATGGTTATTTCT... |
Task1_train_46454 | A genomic change on Chromosome 19 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GACAGTAGAATGTGATTCAAATGCTGAACCGGTGGTCCCCACATTGGTAACTACTGTGTTTATGGAAGGATGCGTTGTCTCTATATCTGTGGTGGCTGCTGAAGTGACCGATATGTCATCCAAAGTGTTGCTCATACTTTGAGGTGAACTGGTCACTGTTTCTAAGCTTGTATCCACCTTGCCTGCGGTCTTTACCAGTGAAGAAGTAAGAACTGAGGACATAGAAACAGGAGAGGAGGTACTGTGCCATTGCGGTGTGAAAGCAACAGAAGAAGGTAAGGTTGTGACAAGGACAGGTGCTTGAGAAGAGGGAGAGCTGG... | GACAGTAGAATGTGATTCAAATGCTGAACCGGTGGTCCCCACATTGGTAACTACTGTGTTTATGGAAGGATGCGTTGTCTCTATATCTGTGGTGGCTGCTGAAGTGACCGATATGTCATCCAAAGTGTTGCTCATACTTTGAGGTGAACTGGTCACTGTTTCTAAGCTTGTATCCACCTTGCCTGCGGTCTTTACCAGTGAAGAAGTAAGAACTGAGGACATAGAAACAGGAGAGGAGGTACTGTGCCATTGCGGTGTGAAAGCAACAGAAGAAGGTAAGGTTGTGACAAGGACAGGTGCTTGAGAAGAGGGAGAGCTGG... |
Task1_train_46455 | This mutation occurs on Chromosome 19. Does this change lead to a known medical condition, or is it benign? | Benign | GGCAAACCCCTCAGTCACCACTGATGGAGTCCCTGCTGAGGTTTCCAAGGTTGATGTGTCTAAGGCAAGTGGAATCTTTGATGTAGCTCCAGAAGACCCTGTCTGGGTGGTGGTCATGTGGGTAGATATTGTCATGGGAGGAGAGTTTGAAAGTCTACTGCTGGCTACTGAGAAAATATCTGGGAACTTTGTTGACTGAGCAGGAGTTGGTATGAATGTTGCATCAAAAGAGGGGACTTCCATTTTTGTGGCTTCAGTAATAGCCCCCACAGACACATTGGAGAGGATGATGTTTGACTCTGTAGTTGAGTTCATCTCCT... | GGCAAACCCCTCAGTCACCACTGATGGAGTCCCTGCTGAGGTTTCCAAGGTTGATGTGTCTAAGGCAAGTGGAATCTTTGATGTAGCTCCAGAAGACCCTGTCTGGGTGGTGGTCATGTGGGTAGATATTGTCATGGGAGGAGAGTTTGAAAGTCTACTGCTGGCTACTGAGAAAATATCTGGGAACTTTGTTGACTGAGCAGGAGTTGGTATGAATGTTGCATCAAAAGAGGGGACTTCCATTTTTGTGGCTTCAGTAATAGCCCCCACAGACACATTGGAGAGGATGATGTTTGACTCTGTAGTTGAGTTCATCTCCT... |
Task1_train_46456 | Given a variant located on Chromosome 19, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TGCATCAAAAGAGGGGACTTCCATTTTTGTGGCTTCAGTAATAGCCCCCACAGACACATTGGAGAGGATGATGTTTGACTCTGTAGTTGAGTTCATCTCCTGGAGGGTGCTGTTCTCTTTTCGTCCAGCAGTCAGGGAGGATGTTGGCTCTCCCTCAATGTCTGTGGTCTCAGAACCAGGTATTGATATAGAAGCAAGAGCGTCCCCCATGCTGGAGGCAGGAACCATTGGAGATGTGGCTGTAGATGGTTCTGAGCTGACTGGGAGAGTGGAATGCAGTACATGTGCTGAACTGGCAGTCCCCATATTGGTCACTGCTT... | TGCATCAAAAGAGGGGACTTCCATTTTTGTGGCTTCAGTAATAGCCCCCACAGACACATTGGAGAGGATGATGTTTGACTCTGTAGTTGAGTTCATCTCCTGGAGGGTGCTGTTCTCTTTTCGTCCAGCAGTCAGGGAGGATGTTGGCTCTCCCTCAATGTCTGTGGTCTCAGAACCAGGTATTGATATAGAAGCAAGAGCGTCCCCCATGCTGGAGGCAGGAACCATTGGAGATGTGGCTGTAGATGGTTCTGAGCTGACTGGGAGAGTGGAATGCAGTACATGTGCTGAACTGGCAGTCCCCATATTGGTCACTGCTT... |
Task1_train_46457 | This alteration on Chromosome 19 may affect genome function. Does it lead to a disease or is it benign? | Benign | GAGGTGAATTGGTCACAGGTTCCATGCTTGTGTTCAACATATCTGTGGTCTTCACCAGTCCAGAGGTAAGAACTGAAGTCGCAGAAACAGGAGAGGATGTATGTTGCCCTTGTAACGTGGAAGTGGCAGGAGGTATGGTTGTGACCAAGAAAGGTGTCAGGGAAGAGGGATAGCTGGTTTCTGCCACAGAGGGAGGGCTTGTCCAGGACACATCCTTGGGACCTTTGCTTATGAGAGTGGTCTTCTCTGATTGCATAAAATCTGGAGTCACAGCTAATGGAGTCTCTGTCAAGTAAGGCATGGTTGATGTGTCCAAGAGA... | GAGGTGAATTGGTCACAGGTTCCATGCTTGTGTTCAACATATCTGTGGTCTTCACCAGTCCAGAGGTAAGAACTGAAGTCGCAGAAACAGGAGAGGATGTATGTTGCCCTTGTAACGTGGAAGTGGCAGGAGGTATGGTTGTGACCAAGAAAGGTGTCAGGGAAGAGGGATAGCTGGTTTCTGCCACAGAGGGAGGGCTTGTCCAGGACACATCCTTGGGACCTTTGCTTATGAGAGTGGTCTTCTCTGATTGCATAAAATCTGGAGTCACAGCTAATGGAGTCTCTGTCAAGTAAGGCATGGTTGATGTGTCCAAGAGA... |
Task1_train_46458 | A variant has been detected on Chromosome 19. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | ACGTGGAAGTGGCAGGAGGTATGGTTGTGACCAAGAAAGGTGTCAGGGAAGAGGGATAGCTGGTTTCTGCCACAGAGGGAGGGCTTGTCCAGGACACATCCTTGGGACCTTTGCTTATGAGAGTGGTCTTCTCTGATTGCATAAAATCTGGAGTCACAGCTAATGGAGTCTCTGTCAAGTAAGGCATGGTTGATGTGTCCAAGAGATATGGACCCTGTGTTGCAGCTCCAGTAGGACCTGTTTGGGTGGTGATGGTCACTCCTGAAGATTCTGTCATTATCAGAGAGGTGGAGGGGTTGGTGCTCACATCTGTAAATGTG... | ACGTGGAAGTGGCAGGAGGTATGGTTGTGACCAAGAAAGGTGTCAGGGAAGAGGGATAGCTGGTTTCTGCCACAGAGGGAGGGCTTGTCCAGGACACATCCTTGGGACCTTTGCTTATGAGAGTGGTCTTCTCTGATTGCATAAAATCTGGAGTCACAGCTAATGGAGTCTCTGTCAAGTAAGGCATGGTTGATGTGTCCAAGAGATATGGACCCTGTGTTGCAGCTCCAGTAGGACCTGTTTGGGTGGTGATGGTCACTCCTGAAGATTCTGTCATTATCAGAGAGGTGGAGGGGTTGGTGCTCACATCTGTAAATGTG... |
Task1_train_46459 | This mutation is located on Chromosome 19. Is it associated with a disease or is it a benign polymorphism? | Benign | TGTCCAAGAGATATGGACCCTGTGTTGCAGCTCCAGTAGGACCTGTTTGGGTGGTGATGGTCACTCCTGAAGATTCTGTCATTATCAGAGAGGTGGAGGGGTTGGTGCTCACATCTGTAAATGTGTTGGTAGAAGTTATAAACTGATGAGGGCTTGAGATGGATGTTCCGCTAGAGAAAGTGGCTTGTGTCTTGGTGACATGAGTAGTAGCATCACCACTAGACACATGGGTAATGACAGTGCTTGTCTCTGTAGCAGAGCTGGCCACCTGGGATGTGCTTCTCTCCTGAAGTCCCTGGTTCACAGAGGACACTGTCTCA... | TGTCCAAGAGATATGGACCCTGTGTTGCAGCTCCAGTAGGACCTGTTTGGGTGGTGATGGTCACTCCTGAAGATTCTGTCATTATCAGAGAGGTGGAGGGGTTGGTGCTCACATCTGTAAATGTGTTGGTAGAAGTTATAAACTGATGAGGGCTTGAGATGGATGTTCCGCTAGAGAAAGTGGCTTGTGTCTTGGTGACATGAGTAGTAGCATCACCACTAGACACATGGGTAATGACAGTGCTTGTCTCTGTAGCAGAGCTGGCCACCTGGGATGTGCTTCTCTCCTGAAGTCCCTGGTTCACAGAGGACACTGTCTCA... |
Task1_train_46460 | This sequence variant lies on Chromosome 19. Is it clinically significant, and what condition might it cause if any? | Benign | TGGTTGCCTCCATATTCGTCACTGCTGTGTCTGCAGAATGATGAATTGCCTTTGTATCTCTGGAGGCTTCATAAGTGGATAACGCCTCACCTGCTGTACTGCTCAAATTGGGAGGTAAACTTGTGCCAGGTTCCAAGCTTATCCTCGACATGTCTGTGGTCTTCCCCAGGCCAGAGGTCTCAGACAAGAAAACTGAGGTCACAGGTGGAGTAGAGGAGGGACTGTGCCCTTGTGATGTCAACAAAATATTGGAAGGCGAGGTTGTAGCATGGATAGGTACCAGGGAAGAGGAAGAGCTGGTTTCTTCCACAGAGGGAGGG... | TGGTTGCCTCCATATTCGTCACTGCTGTGTCTGCAGAATGATGAATTGCCTTTGTATCTCTGGAGGCTTCATAAGTGGATAACGCCTCACCTGCTGTACTGCTCAAATTGGGAGGTAAACTTGTGCCAGGTTCCAAGCTTATCCTCGACATGTCTGTGGTCTTCCCCAGGCCAGAGGTCTCAGACAAGAAAACTGAGGTCACAGGTGGAGTAGAGGAGGGACTGTGCCCTTGTGATGTCAACAAAATATTGGAAGGCGAGGTTGTAGCATGGATAGGTACCAGGGAAGAGGAAGAGCTGGTTTCTTCCACAGAGGGAGGG... |
Task1_train_46461 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TTCCAAGCTTATCCTCGACATGTCTGTGGTCTTCCCCAGGCCAGAGGTCTCAGACAAGAAAACTGAGGTCACAGGTGGAGTAGAGGAGGGACTGTGCCCTTGTGATGTCAACAAAATATTGGAAGGCGAGGTTGTAGCATGGATAGGTACCAGGGAAGAGGAAGAGCTGGTTTCTTCCACAGAGGGAGGGCTTGGCTGTGATGTATCCTCAGGACCTTTGCTAAAGAGAGTGGTCTTCTCTGAGTATGTAAATCTCTGAGTCGTAGCCAGTGGAGTCCCTGTCCAGGAGGCTGTGGCTGATGTATCCAAAGTAGGTGCAC... | TTCCAAGCTTATCCTCGACATGTCTGTGGTCTTCCCCAGGCCAGAGGTCTCAGACAAGAAAACTGAGGTCACAGGTGGAGTAGAGGAGGGACTGTGCCCTTGTGATGTCAACAAAATATTGGAAGGCGAGGTTGTAGCATGGATAGGTACCAGGGAAGAGGAAGAGCTGGTTTCTTCCACAGAGGGAGGGCTTGGCTGTGATGTATCCTCAGGACCTTTGCTAAAGAGAGTGGTCTTCTCTGAGTATGTAAATCTCTGAGTCGTAGCCAGTGGAGTCCCTGTCCAGGAGGCTGTGGCTGATGTATCCAAAGTAGGTGCAC... |
Task1_train_46462 | This is a variant located on Chromosome 19. Is this mutation a likely cause of disease or not? | Benign | TGTGCCCTTGTGATGTCAACAAAATATTGGAAGGCGAGGTTGTAGCATGGATAGGTACCAGGGAAGAGGAAGAGCTGGTTTCTTCCACAGAGGGAGGGCTTGGCTGTGATGTATCCTCAGGACCTTTGCTAAAGAGAGTGGTCTTCTCTGAGTATGTAAATCTCTGAGTCGTAGCCAGTGGAGTCCCTGTCCAGGAGGCTGTGGCTGATGTATCCAAAGTAGGTGCACTTAGTGATGTAGCGCCAGGTGGACTTGTTTGCATAGCAAGGATCATTCCTCCAGATTCTGTCATGGCAGGAAAGTTAGACAGCCTGGTGATG... | TGTGCCCTTGTGATGTCAACAAAATATTGGAAGGCGAGGTTGTAGCATGGATAGGTACCAGGGAAGAGGAAGAGCTGGTTTCTTCCACAGAGGGAGGGCTTGGCTGTGATGTATCCTCAGGACCTTTGCTAAAGAGAGTGGTCTTCTCTGAGTATGTAAATCTCTGAGTCGTAGCCAGTGGAGTCCCTGTCCAGGAGGCTGTGGCTGATGTATCCAAAGTAGGTGCACTTAGTGATGTAGCGCCAGGTGGACTTGTTTGCATAGCAAGGATCATTCCTCCAGATTCTGTCATGGCAGGAAAGTTAGACAGCCTGGTGATG... |
Task1_train_46463 | A variant was discovered on Chromosome 19. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GTGGACTTGTTTGCATAGCAAGGATCATTCCTCCAGATTCTGTCATGGCAGGAAAGTTAGACAGCCTGGTGATGGCTTCTGAGGGGCTGTCTGACGACCTCATAGACTGGGCAAGGAATGAGCTGGATATTCTCTTAGAGGAGGTAATTTCTGTTCTAGGCCCCTTGGTGATCGCAGTGGAACCTGGGGAAGAGATAATACTTGTTTGTGTGGTTGAGCTGGTGTCCATGTAAGGGCTGACGTCCCTCAGTTCAATAGTCAAGAAGGAATTAGGCTCTGTTCTAGCCCTTGTAGACTCTGGCCATGTGGTTGTTGACATA... | GTGGACTTGTTTGCATAGCAAGGATCATTCCTCCAGATTCTGTCATGGCAGGAAAGTTAGACAGCCTGGTGATGGCTTCTGAGGGGCTGTCTGACGACCTCATAGACTGGGCAAGGAATGAGCTGGATATTCTCTTAGAGGAGGTAATTTCTGTTCTAGGCCCCTTGGTGATCGCAGTGGAACCTGGGGAAGAGATAATACTTGTTTGTGTGGTTGAGCTGGTGTCCATGTAAGGGCTGACGTCCCTCAGTTCAATAGTCAAGAAGGAATTAGGCTCTGTTCTAGCCCTTGTAGACTCTGGCCATGTGGTTGTTGACATA... |
Task1_train_46464 | This alteration on Chromosome 19 may affect genome function. Does it lead to a disease or is it benign? | Benign | CGTCCCTCAGTTCAATAGTCAAGAAGGAATTAGGCTCTGTTCTAGCCCTTGTAGACTCTGGCCATGTGGTTGTTGACATAGAAACTATTGCTTGTTCCCTGGTGGAGGTTGTAACCACTGGAGATGTGAGTTTGGATGACGCTGAGTGGGCTGGGATAGTGGAATGAGAAGCATGTTCGGAACTTGTGACCCAGCCTGTGGTCTCTACTGTGTTTGTAGAAGGGTGAATTGCCTCTTTGTCTGTGGTGGACTCAGAAGGGGCAATTCTCTCATATGGGCTGCTTTTCCAACTTGGGGATGAAGTCGTCCCAGATTCCAAG... | CGTCCCTCAGTTCAATAGTCAAGAAGGAATTAGGCTCTGTTCTAGCCCTTGTAGACTCTGGCCATGTGGTTGTTGACATAGAAACTATTGCTTGTTCCCTGGTGGAGGTTGTAACCACTGGAGATGTGAGTTTGGATGACGCTGAGTGGGCTGGGATAGTGGAATGAGAAGCATGTTCGGAACTTGTGACCCAGCCTGTGGTCTCTACTGTGTTTGTAGAAGGGTGAATTGCCTCTTTGTCTGTGGTGGACTCAGAAGGGGCAATTCTCTCATATGGGCTGCTTTTCCAACTTGGGGATGAAGTCGTCCCAGATTCCAAG... |
Task1_train_46465 | This mutation is located on Chromosome 19. Is it associated with a disease or is it a benign polymorphism? | Benign | GTGGGCTGGGATAGTGGAATGAGAAGCATGTTCGGAACTTGTGACCCAGCCTGTGGTCTCTACTGTGTTTGTAGAAGGGTGAATTGCCTCTTTGTCTGTGGTGGACTCAGAAGGGGCAATTCTCTCATATGGGCTGCTTTTCCAACTTGGGGATGAAGTCGTCCCAGATTCCAAGTTTATGTCCAGCGTATTCAGGGTCCTTAATACACTGGAGGAGCTGGTAACCTCCTTGATGGTATCTTCTGAGACAGAATTCATCATCTCAGTGATCCAAGGTGCACTTGGGGTTGATTTTTCTTTCTCATTCCAGGAGTCAGATG... | GTGGGCTGGGATAGTGGAATGAGAAGCATGTTCGGAACTTGTGACCCAGCCTGTGGTCTCTACTGTGTTTGTAGAAGGGTGAATTGCCTCTTTGTCTGTGGTGGACTCAGAAGGGGCAATTCTCTCATATGGGCTGCTTTTCCAACTTGGGGATGAAGTCGTCCCAGATTCCAAGTTTATGTCCAGCGTATTCAGGGTCCTTAATACACTGGAGGAGCTGGTAACCTCCTTGATGGTATCTTCTGAGACAGAATTCATCATCTCAGTGATCCAAGGTGCACTTGGGGTTGATTTTTCTTTCTCATTCCAGGAGTCAGATG... |
Task1_train_46466 | A genetic alteration is present on Chromosome 19. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | AACCTCCTTGATGGTATCTTCTGAGACAGAATTCATCATCTCAGTGATCCAAGGTGCACTTGGGGTTGATTTTTCTTTCTCATTCCAGGAGTCAGATGTAGCTCTTGCCTCTGTTGTAAGAGCTGTCTGCCCTTGTCTCTGAAAAGTTGCATCTGGAGTTTTTGCTGTGTGTGGGATCACATCCAGAGTTGTTGCTGCTGATCTGGGCACCTGCCCTGGATGTGCAGAAGTGGTGGTGGGAAGCTGAGTGGAAGTCTGCTCTGCCTTTTTGCTTGTGGGATCTGGTCTTGAAAAAGTAACTCCAGAGCTCCTTGCCATTG... | AACCTCCTTGATGGTATCTTCTGAGACAGAATTCATCATCTCAGTGATCCAAGGTGCACTTGGGGTTGATTTTTCTTTCTCATTCCAGGAGTCAGATGTAGCTCTTGCCTCTGTTGTAAGAGCTGTCTGCCCTTGTCTCTGAAAAGTTGCATCTGGAGTTTTTGCTGTGTGTGGGATCACATCCAGAGTTGTTGCTGCTGATCTGGGCACCTGCCCTGGATGTGCAGAAGTGGTGGTGGGAAGCTGAGTGGAAGTCTGCTCTGCCTTTTTGCTTGTGGGATCTGGTCTTGAAAAAGTAACTCCAGAGCTCCTTGCCATTG... |
Task1_train_46467 | Assess the clinical impact of this variant found on Chromosome 19. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | ATCCTTTCCCTGTCCTTCAGGAAAATAACATCTACCTGTCAAAGGAGTGAGAAAAATGTGACATCCCAAGAGCACTCCTAGGGACCATATTTCACATTTTTCTAAGCAATTTGGCACTGCCAAGGACTTCAGCCCATAATCCCTTCTTCCGTAGTAACAAACGCAACATTTGCCATCTCAGGTTCACCTAGGCCCTCCCTGTGAACACAGTGATGGTCTCTGATTTAGAAAGATCCTTCACTCTGGAGCAGAAGAAAGTACAGAAAGAATCGACTCTGTAGCATTCTCTCCTGCTGAATTAATTGGCTATTGATCATGTA... | ATCCTTTCCCTGTCCTTCAGGAAAATAACATCTACCTGTCAAAGGAGTGAGAAAAATGTGACATCCCAAGAGCACTCCTAGGGACCATATTTCACATTTTTCTAAGCAATTTGGCACTGCCAAGGACTTCAGCCCATAATCCCTTCTTCCGTAGTAACAAACGCAACATTTGCCATCTCAGGTTCACCTAGGCCCTCCCTGTGAACACAGTGATGGTCTCTGATTTAGAAAGATCCTTCACTCTGGAGCAGAAGAAAGTACAGAAAGAATCGACTCTGTAGCATTCTCTCCTGCTGAATTAATTGGCTATTGATCATGTA... |
Task1_train_46468 | This mutation occurs on Chromosome 19. Does this change lead to a known medical condition, or is it benign? | Benign | TGGATGACAGAGTGAGACTGTCTCTTTAAAAATAAATGAAATAAAATGGAGTAATATTCTGTTTAGAGCATGGATTCTTAACCTCTTTTTATTATAGGTCCCTTTGACAGGCTTGTGAACCATATGAATTCCTTTATAAATTAAAATAAAAATATAGAATAAAACATAAAATAACAATATAAAATATTAGATTACAAAGGAAATCATTGTGGATAAAGAAAATCTGGTACACATACACCTCGGAGTACTATGCAGCCATAAAAAAGAATGAAATCATGTTCTTTAAAGCAACGTGGCTGGAGCTGAAGGCCATCAACCTA... | TGGATGACAGAGTGAGACTGTCTCTTTAAAAATAAATGAAATAAAATGGAGTAATATTCTGTTTAGAGCATGGATTCTTAACCTCTTTTTATTATAGGTCCCTTTGACAGGCTTGTGAACCATATGAATTCCTTTATAAATTAAAATAAAAATATAGAATAAAACATAAAATAACAATATAAAATATTAGATTACAAAGGAAATCATTGTGGATAAAGAAAATCTGGTACACATACACCTCGGAGTACTATGCAGCCATAAAAAAGAATGAAATCATGTTCTTTAAAGCAACGTGGCTGGAGCTGAAGGCCATCAACCTA... |
Task1_train_46469 | A variant found on Chromosome 19 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | ATAAATGAAATAAAATGGAGTAATATTCTGTTTAGAGCATGGATTCTTAACCTCTTTTTATTATAGGTCCCTTTGACAGGCTTGTGAACCATATGAATTCCTTTATAAATTAAAATAAAAATATAGAATAAAACATAAAATAACAATATAAAATATTAGATTACAAAGGAAATCATTGTGGATAAAGAAAATCTGGTACACATACACCTCGGAGTACTATGCAGCCATAAAAAAGAATGAAATCATGTTCTTTAAAGCAACGTGGCTGGAGCTGAAGGCCATCAACCTAAGCAAAATAACTCAAAAACAGAAAATTAAAT... | ATAAATGAAATAAAATGGAGTAATATTCTGTTTAGAGCATGGATTCTTAACCTCTTTTTATTATAGGTCCCTTTGACAGGCTTGTGAACCATATGAATTCCTTTATAAATTAAAATAAAAATATAGAATAAAACATAAAATAACAATATAAAATATTAGATTACAAAGGAAATCATTGTGGATAAAGAAAATCTGGTACACATACACCTCGGAGTACTATGCAGCCATAAAAAAGAATGAAATCATGTTCTTTAAAGCAACGTGGCTGGAGCTGAAGGCCATCAACCTAAGCAAAATAACTCAAAAACAGAAAATTAAAT... |
Task1_train_46470 | This variant is present on Chromosome 19. Is the change likely to result in a pathogenic outcome? | Benign | AACCTAAGCAAAATAACTCAAAAACAGAAAATTAAATACTGCACATTCTCACTTATAAGTGGGAGCTAACCAATGGGTACATGTGGACATAAAGATAGAAATAATAGACACTGGGACTCCAAAATAGAGGAGGCTGGGAGTGAAGTGAGGATTGAAAAACTACTTATTGGGCACAACATTCACTATTTGGCTGATGGGTTCACTAGAAGCCAAACCTCATCATTATGCAGTATATCCACGTAACAAACCTGCACATATACCCCTGAATCTAAAATTTAAAAAACAAAGGAAATGATTATATTGAAATGTTGTTATCAAGA... | AACCTAAGCAAAATAACTCAAAAACAGAAAATTAAATACTGCACATTCTCACTTATAAGTGGGAGCTAACCAATGGGTACATGTGGACATAAAGATAGAAATAATAGACACTGGGACTCCAAAATAGAGGAGGCTGGGAGTGAAGTGAGGATTGAAAAACTACTTATTGGGCACAACATTCACTATTTGGCTGATGGGTTCACTAGAAGCCAAACCTCATCATTATGCAGTATATCCACGTAACAAACCTGCACATATACCCCTGAATCTAAAATTTAAAAAACAAAGGAAATGATTATATTGAAATGTTGTTATCAAGA... |
Task1_train_46471 | A change on Chromosome 19 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TGTAATACAATAATACAGGCACTTATTTTACTAACTCATTAAATAAGATCTATTGAAAAGCCTAATAACCACTATAATTATGAATAAAGTCGTACATGATTTTTAAAAGTGCTTGCAACAATTGTCATAGGATATGAAAGTGTCCGGAATTTCTGTTGTTGGCAAAGGCACAGGCACTGCTAGGATTAATGTGGTTTGTTTTGTTACCTCTATTCATCAATAAAACAAATGCTAAATTTCAGTTCGAGGTTAGCAAAAATAAAGATGTAGTTTACAAATACCGCATGTTCTCACTCATAAGTGGGAATTAAACCTTGAGT... | TGTAATACAATAATACAGGCACTTATTTTACTAACTCATTAAATAAGATCTATTGAAAAGCCTAATAACCACTATAATTATGAATAAAGTCGTACATGATTTTTAAAAGTGCTTGCAACAATTGTCATAGGATATGAAAGTGTCCGGAATTTCTGTTGTTGGCAAAGGCACAGGCACTGCTAGGATTAATGTGGTTTGTTTTGTTACCTCTATTCATCAATAAAACAAATGCTAAATTTCAGTTCGAGGTTAGCAAAAATAAAGATGTAGTTTACAAATACCGCATGTTCTCACTCATAAGTGGGAATTAAACCTTGAGT... |
Task1_train_46472 | Here is a genetic alteration on Chromosome 19. Based on the data, is it a benign variant or a cause of disease? | Benign | AAATGAGCTTGCACTTATGGCCTTTGTGGAAGTCATCATCCTTGCCCTTGGGTTTTTTTCTGGAGACTTGGACAGTGAGGAAGATGCTGTGCTTGCATCTGAGTCTGGAATGGTGTTCAGGGACTGTCCAGGAGTTGGTAAAGAAGCGGACTTAGTATCCAAACTTGGGACCTCAGAAAACTCAAATGTCAAGGTAGACTGTGGGATCCCCCAAGTTGGGGGAGCTGTAGTCAGTGAGGCAAAGGCCTTTGATGGGCTTGAGGAGGCAGAGACAGGTGTTAGGAGGCCTGACTCAGCACTGGTGGGCTTCACAGGTATCC... | AAATGAGCTTGCACTTATGGCCTTTGTGGAAGTCATCATCCTTGCCCTTGGGTTTTTTTCTGGAGACTTGGACAGTGAGGAAGATGCTGTGCTTGCATCTGAGTCTGGAATGGTGTTCAGGGACTGTCCAGGAGTTGGTAAAGAAGCGGACTTAGTATCCAAACTTGGGACCTCAGAAAACTCAAATGTCAAGGTAGACTGTGGGATCCCCCAAGTTGGGGGAGCTGTAGTCAGTGAGGCAAAGGCCTTTGATGGGCTTGAGGAGGCAGAGACAGGTGTTAGGAGGCCTGACTCAGCACTGGTGGGCTTCACAGGTATCC... |
Task1_train_46473 | Consider a variant on Chromosome 19. Determine its clinical classification and disease relevance. | Benign | ATAGGTTGTATTCCGTGGAGCAACAATCTTAGAGGGGGAAGTGGAAGAAGGATGGAGTGGACTTTCTGTTACTCCTTGGATAGTGATTCCAGGGATGCTCCTATCTGGGTTACTTACTGTCTTAAGAACCAGTGCATCACCATTTGAGGTCTCTGACATGGTCAGGGTAGTCTCTGGGACTGTGCCAAGACTATCCGAAGCTATAGTCACCAGTGGGGTGGAATCAAAGGATGTAGCTAATGAACTTGTTGGCTCAGTGGCAGTGAGAGGGATGGCTGGAGTGTCCGGGAGTAAAGTAGGGAAGGAAGCTCCAGACAGAG... | ATAGGTTGTATTCCGTGGAGCAACAATCTTAGAGGGGGAAGTGGAAGAAGGATGGAGTGGACTTTCTGTTACTCCTTGGATAGTGATTCCAGGGATGCTCCTATCTGGGTTACTTACTGTCTTAAGAACCAGTGCATCACCATTTGAGGTCTCTGACATGGTCAGGGTAGTCTCTGGGACTGTGCCAAGACTATCCGAAGCTATAGTCACCAGTGGGGTGGAATCAAAGGATGTAGCTAATGAACTTGTTGGCTCAGTGGCAGTGAGAGGGATGGCTGGAGTGTCCGGGAGTAAAGTAGGGAAGGAAGCTCCAGACAGAG... |
Task1_train_46474 | Chromosome 19 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | TGTAGTTGGGGTCTGTGGTGAAGAATGAATGGCTTTGCTTTCACTCGTAGTGAGAAGACTGGCTTCTGATGTAGCACTGGATCCAGTGACCACTGCTGCTGAGAGATGGGGAGTGAAGGCAGTGGCTGGTTCAATAGTTGATGCTAGAAGTGAGTGTGCCTCTCCTGCAGGACTTGTCTTGAGAAAGCCCATGGCAGGTAAGTCAGTAGTACTGCCTACACTGGTCCATGTACCTGGTGCTGGAACAGAAGTCACCACAGAATTGCTAGAGGTAGGATTTTCTCCGGAGGCAGTGTCAGTGCTGACCATGGTGCTGAAAG... | TGTAGTTGGGGTCTGTGGTGAAGAATGAATGGCTTTGCTTTCACTCGTAGTGAGAAGACTGGCTTCTGATGTAGCACTGGATCCAGTGACCACTGCTGCTGAGAGATGGGGAGTGAAGGCAGTGGCTGGTTCAATAGTTGATGCTAGAAGTGAGTGTGCCTCTCCTGCAGGACTTGTCTTGAGAAAGCCCATGGCAGGTAAGTCAGTAGTACTGCCTACACTGGTCCATGTACCTGGTGCTGGAACAGAAGTCACCACAGAATTGCTAGAGGTAGGATTTTCTCCGGAGGCAGTGTCAGTGCTGACCATGGTGCTGAAAG... |
Task1_train_46475 | A genomic change on Chromosome 19 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | AAGTGAGGCTGAGGAATATGGAGAGGATGTGCTGCTTCCAGAAGAGACTGAATTCTCATGGGTAGGGGAAGCAGACACTGCCACAGAGTTGACATATGGAGTTGACTGTGTCTGCACAGAAACTTTTTCTGAAGAAACTGCATGTAGTGGTTGAGTGGACTGTTCAATTGTGCCTGTACTGGTCCATACAATTGTTGGTGGGGTGATGGGAGAATGTGTCATGGGTGCTGAGTTGATGTCTGGTCCTGAGGTTATGCCTGTAGAAATGACTTCTTCCACTGGAATGGATGAAAAAGGCAATGTTAAGCTTATGGCCCTGT... | AAGTGAGGCTGAGGAATATGGAGAGGATGTGCTGCTTCCAGAAGAGACTGAATTCTCATGGGTAGGGGAAGCAGACACTGCCACAGAGTTGACATATGGAGTTGACTGTGTCTGCACAGAAACTTTTTCTGAAGAAACTGCATGTAGTGGTTGAGTGGACTGTTCAATTGTGCCTGTACTGGTCCATACAATTGTTGGTGGGGTGATGGGAGAATGTGTCATGGGTGCTGAGTTGATGTCTGGTCCTGAGGTTATGCCTGTAGAAATGACTTCTTCCACTGGAATGGATGAAAAAGGCAATGTTAAGCTTATGGCCCTGT... |
Task1_train_46476 | A variant found on Chromosome 19 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GTGAATCTGTGGTATTGGGGGCATTACTGAGAGTGAGAGAAATCCATGGTGTCACCTCCATTGATGGAGTTGGAGATGGAAGATCCATAGAGGCAGTTCTGAGTTTTTCTTTTCCTGTATTTTCAGTGCTTCCCAAAGCTGTGGACATAAGGGTAGCTGAGCTGGACTCTGTCCTTGCTGAAGACTTGGAGATGTCTGAGGTCATAACTGTGGTGACCTCCTTGGTCCAAAATGTGCTGCCCCCTATGAATTCCACATCAGGAGTTGTAGGAGATGAGGTTAGAGGGATGCTTGTGCTCATCTGGCTTCCTTCAGCATAG... | GTGAATCTGTGGTATTGGGGGCATTACTGAGAGTGAGAGAAATCCATGGTGTCACCTCCATTGATGGAGTTGGAGATGGAAGATCCATAGAGGCAGTTCTGAGTTTTTCTTTTCCTGTATTTTCAGTGCTTCCCAAAGCTGTGGACATAAGGGTAGCTGAGCTGGACTCTGTCCTTGCTGAAGACTTGGAGATGTCTGAGGTCATAACTGTGGTGACCTCCTTGGTCCAAAATGTGCTGCCCCCTATGAATTCCACATCAGGAGTTGTAGGAGATGAGGTTAGAGGGATGCTTGTGCTCATCTGGCTTCCTTCAGCATAG... |
Task1_train_46477 | With a mutation on Chromosome 19, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TAATGACTGGCTGATGCTTCTTCCTGGAGCACTAGTAACAAGGAGTCCCATTGTCCCAGCCATAGAGACAGTGGCTGTAGAACTTCTTCTTTCCAGTGCCATGTTTGTGGATGTCTCAGCTGGGGAGGATGTTCCTATGGGAAGGTGGGCTATGCCCAGGGTGACTCCACTACTACTGCTCCCTGTTGTTGTGTTGTCCATGGGTGGAGTGGATTGAATGTTTGTTGGGCCAGTCTCAATCTCTCTGGACAGTGTGTCTGTAGATGGTTTCCAAAAAGTGGTTGCCTCAGAGGAGCTTCTCCCTTGTGTCCCGAGCTCAG... | TAATGACTGGCTGATGCTTCTTCCTGGAGCACTAGTAACAAGGAGTCCCATTGTCCCAGCCATAGAGACAGTGGCTGTAGAACTTCTTCTTTCCAGTGCCATGTTTGTGGATGTCTCAGCTGGGGAGGATGTTCCTATGGGAAGGTGGGCTATGCCCAGGGTGACTCCACTACTACTGCTCCCTGTTGTTGTGTTGTCCATGGGTGGAGTGGATTGAATGTTTGTTGGGCCAGTCTCAATCTCTCTGGACAGTGTGTCTGTAGATGGTTTCCAAAAAGTGGTTGCCTCAGAGGAGCTTCTCCCTTGTGTCCCGAGCTCAG... |
Task1_train_46478 | Here is a genetic alteration on Chromosome 19. Based on the data, is it a benign variant or a cause of disease? | Benign | TGTGGCTGGAGATGGAGTGTCCAAGGGAACCAGGGTGCTTTTTCCTATGGCACCACTTGTTGGAATATTACTTGGTGTCAAGGAAGTCGTGGAAGGTAAGTTGGGCATGTTCCACCGACTAGTTTCAACTGTGTCCATTATCATGCTTGTGGTGACTCTCTGAGTTGAAAATGTGGAGCTCATTGTGACTTTGGGAGTAGGAGAAGAAGGAGATGAGGACAAGATGCCAAGCCAGGTGCTTCTAGCAGAGCCAGGATCAGGAGATGGAGGGTGAGTTGCAGTCATTTGTGGAGTCAGAGCTGAGCTTGTTCCATCTCTAG... | TGTGGCTGGAGATGGAGTGTCCAAGGGAACCAGGGTGCTTTTTCCTATGGCACCACTTGTTGGAATATTACTTGGTGTCAAGGAAGTCGTGGAAGGTAAGTTGGGCATGTTCCACCGACTAGTTTCAACTGTGTCCATTATCATGCTTGTGGTGACTCTCTGAGTTGAAAATGTGGAGCTCATTGTGACTTTGGGAGTAGGAGAAGAAGGAGATGAGGACAAGATGCCAAGCCAGGTGCTTCTAGCAGAGCCAGGATCAGGAGATGGAGGGTGAGTTGCAGTCATTTGTGGAGTCAGAGCTGAGCTTGTTCCATCTCTAG... |
Task1_train_46479 | A mutation is present on Chromosome 19. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TGGTCTCTGTTGTGAGGATGGTTGTTGATGGTTCCCTGATAGAAGTTGCTTCCATGGAACTAGTTGCTGGAGAAGTGAATTTAGAGACCATTACAGTAGCAGAGAGAGAAGTGGCAGAGGTTGAAACAGTGGTTGTTGCTGAAGGTAACCCTGTCTTGAATCTGGGACTAGTCTCTGGCCAAGTTGTGCTTTGGGGTGCAGCAGAGTCATTAAACGTGTCTCTATTGGTCTGTGACATTGTTGCCGTCCCAGTGAGGTGAGATATTTTAGGAAGAGCTGAACCAGTTGAGTTTGTAACTGAGGTACTGCTCGTAGCTCTG... | TGGTCTCTGTTGTGAGGATGGTTGTTGATGGTTCCCTGATAGAAGTTGCTTCCATGGAACTAGTTGCTGGAGAAGTGAATTTAGAGACCATTACAGTAGCAGAGAGAGAAGTGGCAGAGGTTGAAACAGTGGTTGTTGCTGAAGGTAACCCTGTCTTGAATCTGGGACTAGTCTCTGGCCAAGTTGTGCTTTGGGGTGCAGCAGAGTCATTAAACGTGTCTCTATTGGTCTGTGACATTGTTGCCGTCCCAGTGAGGTGAGATATTTTAGGAAGAGCTGAACCAGTTGAGTTTGTAACTGAGGTACTGCTCGTAGCTCTG... |
Task1_train_46480 | A genetic alteration is present on Chromosome 19. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GTCCCCACCAGCAACAGGGCTCTCACCAGGTGTGCCCCTCTGGATTTCAACTTTCCAGCCTCCATATCTGTAATAGATACATTATTTTTCTTTGTAAATTACCCAGTTTCAGCTGTTCTGCTATAAGCAATGCAATACAGACTAAGATAGGCATGGCTCATGGATTTCTCTCAAGATGAGGCCCACCTTGGTTCTAAGCTGCGTCTCCTAGGAATTGAGTTTTTCCCTAGGCCGGTGGGGTAAGTGAAACTATAATTCATTCCTCATGCTTTCCCAATCTTCTTTTCTACTCAGGAGCTACCAATTTTATCCAGGTCAAA... | GTCCCCACCAGCAACAGGGCTCTCACCAGGTGTGCCCCTCTGGATTTCAACTTTCCAGCCTCCATATCTGTAATAGATACATTATTTTTCTTTGTAAATTACCCAGTTTCAGCTGTTCTGCTATAAGCAATGCAATACAGACTAAGATAGGCATGGCTCATGGATTTCTCTCAAGATGAGGCCCACCTTGGTTCTAAGCTGCGTCTCCTAGGAATTGAGTTTTTCCCTAGGCCGGTGGGGTAAGTGAAACTATAATTCATTCCTCATGCTTTCCCAATCTTCTTTTCTACTCAGGAGCTACCAATTTTATCCAGGTCAAA... |
Task1_train_46481 | A variant was discovered on Chromosome 19. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TCCCGAGTAGCTGGGATTACAGGCTCCAGCTACCACACATGGCTAACTTTTGTATTTTTAGTAGAGATGGGGTTTCACCACGTGGGCCAGGCCAGTTTTGAACTCCTGACCTCAAGTGATCCACCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGTGCCCAGCCCAGGGCTCCTATTCTTTAAACTGGAACCTAAGGTATCCTCACTTATGAAGTTCAAATATCTCACAATAATCTCAAATCACTAAGATAATCTAATCATGCTAATTTTTTGATGATAAAACTGAGTATAATAGATGCTAATGT... | TCCCGAGTAGCTGGGATTACAGGCTCCAGCTACCACACATGGCTAACTTTTGTATTTTTAGTAGAGATGGGGTTTCACCACGTGGGCCAGGCCAGTTTTGAACTCCTGACCTCAAGTGATCCACCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGTGCCCAGCCCAGGGCTCCTATTCTTTAAACTGGAACCTAAGGTATCCTCACTTATGAAGTTCAAATATCTCACAATAATCTCAAATCACTAAGATAATCTAATCATGCTAATTTTTTGATGATAAAACTGAGTATAATAGATGCTAATGT... |
Task1_train_46482 | A mutation is present on Chromosome 19. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | ATTTTTAGTAGAGATGGGGTTTCACCACGTGGGCCAGGCCAGTTTTGAACTCCTGACCTCAAGTGATCCACCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGTGCCCAGCCCAGGGCTCCTATTCTTTAAACTGGAACCTAAGGTATCCTCACTTATGAAGTTCAAATATCTCACAATAATCTCAAATCACTAAGATAATCTAATCATGCTAATTTTTTGATGATAAAACTGAGTATAATAGATGCTAATGTTGTCTAGGGAGAATATAGTTTACCAGTGACTGGTCCCAGTAGTTACTAAATTG... | ATTTTTAGTAGAGATGGGGTTTCACCACGTGGGCCAGGCCAGTTTTGAACTCCTGACCTCAAGTGATCCACCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGTGCCCAGCCCAGGGCTCCTATTCTTTAAACTGGAACCTAAGGTATCCTCACTTATGAAGTTCAAATATCTCACAATAATCTCAAATCACTAAGATAATCTAATCATGCTAATTTTTTGATGATAAAACTGAGTATAATAGATGCTAATGTTGTCTAGGGAGAATATAGTTTACCAGTGACTGGTCCCAGTAGTTACTAAATTG... |
Task1_train_46483 | The following genetic variant occurs on Chromosome 19. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GATTGTGCCACTGCACTTCAGCCTGGGTGACAGAGCCAGGCTGTCTAAAAAAAAAAGAAAGCCAAAAGAAGAAGGAGTAAGTGAATTATTCTCTACATTCCCTACCTCTGATATATTTGCAAAGAAATGTAGCTCTCTTTATTATTTGAGTATATTATAATCAACATTTCTTTCACTAAAGCCGACTTCTTCACTGATCAAGATAGAATATCTCACCACTAGGCCGGGCACAGTGGCTCACACCTGTAATCCTAGCACTTTTGGGAGGCTGAGGTGGGCGGATCCAAAGGTCAGGAGTTTGAGACTAGCCTCGCTAATAC... | GATTGTGCCACTGCACTTCAGCCTGGGTGACAGAGCCAGGCTGTCTAAAAAAAAAAGAAAGCCAAAAGAAGAAGGAGTAAGTGAATTATTCTCTACATTCCCTACCTCTGATATATTTGCAAAGAAATGTAGCTCTCTTTATTATTTGAGTATATTATAATCAACATTTCTTTCACTAAAGCCGACTTCTTCACTGATCAAGATAGAATATCTCACCACTAGGCCGGGCACAGTGGCTCACACCTGTAATCCTAGCACTTTTGGGAGGCTGAGGTGGGCGGATCCAAAGGTCAGGAGTTTGAGACTAGCCTCGCTAATAC... |
Task1_train_46484 | This genomic variant is located on Chromosome 19. Can you determine its pathogenicity and name any linked disease? | Benign | CACTTTTGGGAGGCTGAGGTGGGCGGATCCAAAGGTCAGGAGTTTGAGACTAGCCTCGCTAATACGGCAAAACCCCATCTCTACTAAAAATACAAAGATTAGCCAGGTGTGGTGGCAGCTGTCTGTAGTCCCAGCTACTGAGGAGGCTGAGGCAGGAGAATAGCTTGAATCTGGGAGGTGGAGTTTGCAGTGAGCTAAGATTGCACCGCTGCACTCCAGCCTGGGTGACAAGAGCGAGACTCTGTCTCTCAAAAAAAAAAAAAAAAAAAGAAAGAAAGAAAGAAAGAAAATCTCACCACTGAAATAATCTAATGATAGCA... | CACTTTTGGGAGGCTGAGGTGGGCGGATCCAAAGGTCAGGAGTTTGAGACTAGCCTCGCTAATACGGCAAAACCCCATCTCTACTAAAAATACAAAGATTAGCCAGGTGTGGTGGCAGCTGTCTGTAGTCCCAGCTACTGAGGAGGCTGAGGCAGGAGAATAGCTTGAATCTGGGAGGTGGAGTTTGCAGTGAGCTAAGATTGCACCGCTGCACTCCAGCCTGGGTGACAAGAGCGAGACTCTGTCTCTCAAAAAAAAAAAAAAAAAAAGAAAGAAAGAAAGAAAGAAAATCTCACCACTGAAATAATCTAATGATAGCA... |
Task1_train_46485 | A mutation on Chromosome 19 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GGTCAGGAGTTTGAGACTAGCCTCGCTAATACGGCAAAACCCCATCTCTACTAAAAATACAAAGATTAGCCAGGTGTGGTGGCAGCTGTCTGTAGTCCCAGCTACTGAGGAGGCTGAGGCAGGAGAATAGCTTGAATCTGGGAGGTGGAGTTTGCAGTGAGCTAAGATTGCACCGCTGCACTCCAGCCTGGGTGACAAGAGCGAGACTCTGTCTCTCAAAAAAAAAAAAAAAAAAAGAAAGAAAGAAAGAAAGAAAATCTCACCACTGAAATAATCTAATGATAGCAATTTTATTGATGATAAAACTGAGGGTAGTAAGT... | GGTCAGGAGTTTGAGACTAGCCTCGCTAATACGGCAAAACCCCATCTCTACTAAAAATACAAAGATTAGCCAGGTGTGGTGGCAGCTGTCTGTAGTCCCAGCTACTGAGGAGGCTGAGGCAGGAGAATAGCTTGAATCTGGGAGGTGGAGTTTGCAGTGAGCTAAGATTGCACCGCTGCACTCCAGCCTGGGTGACAAGAGCGAGACTCTGTCTCTCAAAAAAAAAAAAAAAAAAAGAAAGAAAGAAAGAAAGAAAATCTCACCACTGAAATAATCTAATGATAGCAATTTTATTGATGATAAAACTGAGGGTAGTAAGT... |
Task1_train_46486 | Chromosome 19 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AAAAAAAAAAAAAAAAAGAAAGAAAGAAAGAAAGAAAATCTCACCACTGAAATAATCTAATGATAGCAATTTTATTGATGATAAAACTGAGGGTAGTAAGTAGACGTTGATGTTGACCTGCACAGACAGTTTAGCAGTGACCGGGCTCTAAAATTACAGAATTCTGGTATCAACAATCAGCTCCCATTTTGCACAATAGGTTTCACTCTGGCATGCATTTCATATGGCCCTAAATATTCAATCAGGCAGTATCAATTCTGTGTTGCGAACACAGCCTTCTTTGGATTCTTGCCCTGACCTGTGAGACGCCTCCTGCTTTT... | AAAAAAAAAAAAAAAAAGAAAGAAAGAAAGAAAGAAAATCTCACCACTGAAATAATCTAATGATAGCAATTTTATTGATGATAAAACTGAGGGTAGTAAGTAGACGTTGATGTTGACCTGCACAGACAGTTTAGCAGTGACCGGGCTCTAAAATTACAGAATTCTGGTATCAACAATCAGCTCCCATTTTGCACAATAGGTTTCACTCTGGCATGCATTTCATATGGCCCTAAATATTCAATCAGGCAGTATCAATTCTGTGTTGCGAACACAGCCTTCTTTGGATTCTTGCCCTGACCTGTGAGACGCCTCCTGCTTTT... |
Task1_train_46487 | A variant affecting Chromosome 19 has been observed. Determine if it's benign or associated with disease. | Benign | TTCAAGGCCCGCCTGGCCAACATGGTGAAACTCTGTCTCTACTAAAAATACAAAAATGAGCCAGGCACAGTAGCAGGCGCCTGTAATCCCAGCTATTCAGGAGGCTGAGGCAGGAGAATCGCTTGAGCCCCAGAGGTGGAGGTTGCAGTAAGCCGAAATTGAGCCACTGCACTCTAGACTGGGCGACAGAGCAAGACTCTGTCTCAATAAATAAATAAATAAATAAATAAATAAATAAGTTTTTAAATTTTTAATTAAATTTAATTTTTTTTAAAAAAAGACTTAGTATTGGATAGACCAGTAGGGTGACTATAGTTCAA... | TTCAAGGCCCGCCTGGCCAACATGGTGAAACTCTGTCTCTACTAAAAATACAAAAATGAGCCAGGCACAGTAGCAGGCGCCTGTAATCCCAGCTATTCAGGAGGCTGAGGCAGGAGAATCGCTTGAGCCCCAGAGGTGGAGGTTGCAGTAAGCCGAAATTGAGCCACTGCACTCTAGACTGGGCGACAGAGCAAGACTCTGTCTCAATAAATAAATAAATAAATAAATAAATAAATAAGTTTTTAAATTTTTAATTAAATTTAATTTTTTTTAAAAAAAGACTTAGTATTGGATAGACCAGTAGGGTGACTATAGTTCAA... |
Task1_train_46488 | Consider a variant on Chromosome 19. Determine its clinical classification and disease relevance. | Benign | CAAGATTGGCCCTGCCTAACATCACCTGTAGTGAGACACCTAAGGGGTTTGTGCTCCCAGATTCCACGGCTCTGATTTCTGTGGGCTTATAGGGCTTGTATTTCAAAGGGATAGCATGTCAGACTCATTCTGGCCAGTATATTACTAGGAACCATTTGACCCAACCAGCTTTCAAATATAGAGTCATAATTTGAAGTTGAAAATCACATTATCATTCTTTGCTTTTGTGTTTGTTTTTGGTTTGAGACAGGGTCTTGCTCTGTCACCCAGGCTGGATTGCAGTGCCACGATCACAGCTCACTACAGCCTCAAACTCCTAG... | CAAGATTGGCCCTGCCTAACATCACCTGTAGTGAGACACCTAAGGGGTTTGTGCTCCCAGATTCCACGGCTCTGATTTCTGTGGGCTTATAGGGCTTGTATTTCAAAGGGATAGCATGTCAGACTCATTCTGGCCAGTATATTACTAGGAACCATTTGACCCAACCAGCTTTCAAATATAGAGTCATAATTTGAAGTTGAAAATCACATTATCATTCTTTGCTTTTGTGTTTGTTTTTGGTTTGAGACAGGGTCTTGCTCTGTCACCCAGGCTGGATTGCAGTGCCACGATCACAGCTCACTACAGCCTCAAACTCCTAG... |
Task1_train_46489 | A genomic change on Chromosome 19 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GGCAGGTAAACCTTATTGTTTAGATCAAGATACATTTTAGAGTTTCACATGATTCCAGCCACAACGAAAGTAATGCCAAAGTATTTTAACATTACCTTGGCCAGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGAAAGGCAGAGGTGGGCAGATTACTTGAGGTCAGAAGTTTGAGACCAGCCTGGCCAACATGGTGAAACTCCATCTCTACTAAAAATACAAAAATCAGCTGTGCATGGTGGGGCGTGCGCCTGTAGTCCCAGCTACTCGGGAAGCTGAGGCATAAGAATCGCTTGAACCCAGGAGGCGGAGGC... | GGCAGGTAAACCTTATTGTTTAGATCAAGATACATTTTAGAGTTTCACATGATTCCAGCCACAACGAAAGTAATGCCAAAGTATTTTAACATTACCTTGGCCAGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGAAAGGCAGAGGTGGGCAGATTACTTGAGGTCAGAAGTTTGAGACCAGCCTGGCCAACATGGTGAAACTCCATCTCTACTAAAAATACAAAAATCAGCTGTGCATGGTGGGGCGTGCGCCTGTAGTCCCAGCTACTCGGGAAGCTGAGGCATAAGAATCGCTTGAACCCAGGAGGCGGAGGC... |
Task1_train_46490 | A mutation has occurred on Chromosome 19. What is the medical relevance of this mutation? | Benign | GAGGTGGGCAGATTACTTGAGGTCAGAAGTTTGAGACCAGCCTGGCCAACATGGTGAAACTCCATCTCTACTAAAAATACAAAAATCAGCTGTGCATGGTGGGGCGTGCGCCTGTAGTCCCAGCTACTCGGGAAGCTGAGGCATAAGAATCGCTTGAACCCAGGAGGCGGAGGCTGCAGTGAGCTGAGATCATGCCACTGCATTCCAGCCTGGTGACAGGCTCAAAACTTCGAGACTCAGGTCTTAAAAAAAAAAATTAAAAGCATTTTAACATTATATTAATGTTCTGTCATCCACAGGTACGTTGCACACTATCAACA... | GAGGTGGGCAGATTACTTGAGGTCAGAAGTTTGAGACCAGCCTGGCCAACATGGTGAAACTCCATCTCTACTAAAAATACAAAAATCAGCTGTGCATGGTGGGGCGTGCGCCTGTAGTCCCAGCTACTCGGGAAGCTGAGGCATAAGAATCGCTTGAACCCAGGAGGCGGAGGCTGCAGTGAGCTGAGATCATGCCACTGCATTCCAGCCTGGTGACAGGCTCAAAACTTCGAGACTCAGGTCTTAAAAAAAAAAATTAAAAGCATTTTAACATTATATTAATGTTCTGTCATCCACAGGTACGTTGCACACTATCAACA... |
Task1_train_46491 | A variant on Chromosome 19 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | CATACTATATTTCTAATTTGAGGATATACTGTGTTCTTGGATAAGGAGGCAAATTGTAACTACACTCTATGTGTATGTTGTTACCCTTTAGTAAGAAGAAGCTTCCCAGCCTGCTAGTGTTGAACATCTAGCAGGCCTAGACTCTAATGGCTTCTGTGTTCTCCTCTAGCTCTGCCTGCTTAGGACTCTGCCCAGCCAGGAAGGAAACCTACAGGAGGAAGAATGGCTGCAGGGTGGCTGACAACCTGGTCACAGGTACACAAGAAATTTCTCTATTTCCAAAAGCACACTGCCATTCCTGAAAAGAACACATCTCTTGC... | CATACTATATTTCTAATTTGAGGATATACTGTGTTCTTGGATAAGGAGGCAAATTGTAACTACACTCTATGTGTATGTTGTTACCCTTTAGTAAGAAGAAGCTTCCCAGCCTGCTAGTGTTGAACATCTAGCAGGCCTAGACTCTAATGGCTTCTGTGTTCTCCTCTAGCTCTGCCTGCTTAGGACTCTGCCCAGCCAGGAAGGAAACCTACAGGAGGAAGAATGGCTGCAGGGTGGCTGACAACCTGGTCACAGGTACACAAGAAATTTCTCTATTTCCAAAAGCACACTGCCATTCCTGAAAAGAACACATCTCTTGC... |
Task1_train_46492 | A variant found on Chromosome 19 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GCCTTGGCCAGTGAGGGTTAGTACATTTGGGAATGTCACTCAGTGAAGGAAAAGAAATCTGAGGCCATGACATGAGCTTCCTTCCTGTTTCACCATCTATTCAATCGTTCATACGTTCATTTGGTCTCCGAGAAAGAAGTTTTAATTCCTCTTTAAATGTAATGTCTCCATGAATGCTTTTTGCCAGATAATACTGTCTTATTTCCCAACCTCCACAATCCTTTCTAACTAAAATACCTCCCATTTCTACTGCTTGTTCCTATCACTGGTGAATCACTGGTTGTGTCTTCTTTCTTACATTTCTCTACTTAGAAGATATT... | GCCTTGGCCAGTGAGGGTTAGTACATTTGGGAATGTCACTCAGTGAAGGAAAAGAAATCTGAGGCCATGACATGAGCTTCCTTCCTGTTTCACCATCTATTCAATCGTTCATACGTTCATTTGGTCTCCGAGAAAGAAGTTTTAATTCCTCTTTAAATGTAATGTCTCCATGAATGCTTTTTGCCAGATAATACTGTCTTATTTCCCAACCTCCACAATCCTTTCTAACTAAAATACCTCCCATTTCTACTGCTTGTTCCTATCACTGGTGAATCACTGGTTGTGTCTTCTTTCTTACATTTCTCTACTTAGAAGATATT... |
Task1_train_46493 | This alteration occurs on Chromosome 19. Is it associated with a disease or is it a benign variant? | Benign | AGACTGAACTGTGTATACACTCTTCCCCGCACAATGTTCATATCTTCGAATCCCAACTCCTAAGGTGTTTATATTTGAATATGGGGGCTTCTAGAGGTAATTAGGGTTGGATGAGATCATGATGATGGGGCTCTCATGATAGTATTAGTACCTTATAAAGAAGAGACACAAGAGTGTTTGCTGTATCTGTCAGCCAAAGGTGAGCCAGCAGAATGAGAGATAATGAGAAAGCAGCACTCTACAAGCCAAGAAGATGCCCTCACCAAAAACCAACCATGTTGGCACCCTGAAGACATTTACAGCCTCCATAGCACTGAGAA... | AGACTGAACTGTGTATACACTCTTCCCCGCACAATGTTCATATCTTCGAATCCCAACTCCTAAGGTGTTTATATTTGAATATGGGGGCTTCTAGAGGTAATTAGGGTTGGATGAGATCATGATGATGGGGCTCTCATGATAGTATTAGTACCTTATAAAGAAGAGACACAAGAGTGTTTGCTGTATCTGTCAGCCAAAGGTGAGCCAGCAGAATGAGAGATAATGAGAAAGCAGCACTCTACAAGCCAAGAAGATGCCCTCACCAAAAACCAACCATGTTGGCACCCTGAAGACATTTACAGCCTCCATAGCACTGAGAA... |
Task1_train_46494 | Here is a mutation located on Chromosome 19. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | AATATGAATTTATCTCAGCACAACCAGACTAGGAGATCTCTTTTTTTTTTGAAATGGACTCTTACTCTGTTGCCCAGGCTGGAGTGCACTGGTGCAATCTTGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCAACTCTCCTGCTTCAGCCTCCTGAGTAGCTGAAATTACAGGCACACGCCACCATGCCCGGCTAATTTTTTGTATTTTTAGTAGAGATAGGGTTTCAGCATACTGGCTAGGTTGGTCTCGAACTCCTGACCTCATGATCCGCCCCCTTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCAC... | AATATGAATTTATCTCAGCACAACCAGACTAGGAGATCTCTTTTTTTTTTGAAATGGACTCTTACTCTGTTGCCCAGGCTGGAGTGCACTGGTGCAATCTTGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCAACTCTCCTGCTTCAGCCTCCTGAGTAGCTGAAATTACAGGCACACGCCACCATGCCCGGCTAATTTTTTGTATTTTTAGTAGAGATAGGGTTTCAGCATACTGGCTAGGTTGGTCTCGAACTCCTGACCTCATGATCCGCCCCCTTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCAC... |
Task1_train_46495 | Consider this mutation on Chromosome 19. Is this a benign change or a disease-causing variant? | Benign | ACTTTGGGAGGCCGAAGCGGGCGGATCACAAGGTCAGGAGATCGAGACCATCCCGGCTAAAACGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCGGGCGTAGTGGCGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCGAGATCCCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGTATTACCAGATTTTTTTTTTTTTTGAGATGGAGTTTTGC... | ACTTTGGGAGGCCGAAGCGGGCGGATCACAAGGTCAGGAGATCGAGACCATCCCGGCTAAAACGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCGGGCGTAGTGGCGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCGAGATCCCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGTATTACCAGATTTTTTTTTTTTTTGAGATGGAGTTTTGC... |
Task1_train_46496 | A genomic change on Chromosome 19 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | GTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCGAGATCCCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGTATTACCAGATTTTTTTTTTTTTTGAGATGGAGTTTTGCTCTGTCACCCAGGCTGGAGTGTAGTGGCAAAATCTTGGCTCACTGCAACCTCTGTCTCCTGGGTTCACACAATTCTCCTGCCTCAGCCTCCCAAGCAATTGGGATTAAAGGCACCCGCCACCATAC... | GTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCGAGATCCCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGTATTACCAGATTTTTTTTTTTTTTGAGATGGAGTTTTGCTCTGTCACCCAGGCTGGAGTGTAGTGGCAAAATCTTGGCTCACTGCAACCTCTGTCTCCTGGGTTCACACAATTCTCCTGCCTCAGCCTCCCAAGCAATTGGGATTAAAGGCACCCGCCACCATAC... |
Task1_train_46497 | The following genetic variant occurs on Chromosome 19. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | ATTTTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGCTGGTCTCAAACTCCCGACCTTGTGATCCACTGTCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACGCCTGGCCTTTTTTTTTCTTTTGAAACAAAGTCTCACTGTTTTTCCCAGGCTGGCGGGCAGTGGCACAATCACGGCTCACTGCAGCCTCGACCTCCCAGGCTCAAGCAATCCTCTCACCTCAGCCCCCCGGAATAGCAGGGACTACAGGCACAAGTCACCACGCCCAGCTTATTTATTGTATCTTTAGTAGAGACAAGGTCTCGC... | ATTTTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGCTGGTCTCAAACTCCCGACCTTGTGATCCACTGTCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACGCCTGGCCTTTTTTTTTCTTTTGAAACAAAGTCTCACTGTTTTTCCCAGGCTGGCGGGCAGTGGCACAATCACGGCTCACTGCAGCCTCGACCTCCCAGGCTCAAGCAATCCTCTCACCTCAGCCCCCCGGAATAGCAGGGACTACAGGCACAAGTCACCACGCCCAGCTTATTTATTGTATCTTTAGTAGAGACAAGGTCTCGC... |
Task1_train_46498 | The following genetic variant occurs on Chromosome 19. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | ATCTTTAGTAGAGACAAGGTCTCGCAATGTTGCCCAGGCTAGTCTCAAACTCCTGAGCTCAAGTGATCTGCCTGCCTCGGCCTCCTAAAGTGCTGGGATTACAGGCGTGAGCCACTGCACCTGGCCACTATTGATCTTAAAACAGACCCTAAGTGGACAATGCTCCATCCCAAAGGACCCAGGGAACTGCAGCCCCTGGGGAGTCACTGGGCCCAGGAATTCCCTGGTCATTGAATATTGGGTGGTTAGTGGTCACTGGACAGCCATTGAATGATAAGACATCACTTGAATTCACTGCCATGGTTAACTAACCCCTGTCA... | ATCTTTAGTAGAGACAAGGTCTCGCAATGTTGCCCAGGCTAGTCTCAAACTCCTGAGCTCAAGTGATCTGCCTGCCTCGGCCTCCTAAAGTGCTGGGATTACAGGCGTGAGCCACTGCACCTGGCCACTATTGATCTTAAAACAGACCCTAAGTGGACAATGCTCCATCCCAAAGGACCCAGGGAACTGCAGCCCCTGGGGAGTCACTGGGCCCAGGAATTCCCTGGTCATTGAATATTGGGTGGTTAGTGGTCACTGGACAGCCATTGAATGATAAGACATCACTTGAATTCACTGCCATGGTTAACTAACCCCTGTCA... |
Task1_train_46499 | A variant has been detected on Chromosome 19. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TGCCTAGCTAATTAAAAAAAATTTTTTTGTAAAGAGGCCAAACTTCTGGTTTAAGCTGACTTGGGCCTCCCAGCCCAAGCTGACAATTTTCAACTTTTCCTCTAGGAGCCTGGGTGAATAAATAGGCCTATAATCTCCAGTGAGTCTCATTATAATTGCATTCCCAAAAGACATACCTAATTAATACAGGTGGTGACAGGTACCTCAGATGAGACAAGAGCCAGATCCCAAGACAGATATGGGCCACATCAGATGAAAGAGATCAAGAGCTGGGTGAGGTGGCTCGTACCTGTAATCTCAGCAGCTCAGGAGGCTGAGGT... | TGCCTAGCTAATTAAAAAAAATTTTTTTGTAAAGAGGCCAAACTTCTGGTTTAAGCTGACTTGGGCCTCCCAGCCCAAGCTGACAATTTTCAACTTTTCCTCTAGGAGCCTGGGTGAATAAATAGGCCTATAATCTCCAGTGAGTCTCATTATAATTGCATTCCCAAAAGACATACCTAATTAATACAGGTGGTGACAGGTACCTCAGATGAGACAAGAGCCAGATCCCAAGACAGATATGGGCCACATCAGATGAAAGAGATCAAGAGCTGGGTGAGGTGGCTCGTACCTGTAATCTCAGCAGCTCAGGAGGCTGAGGT... |
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