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_45200 | This genomic variant is located on Chromosome 17. Can you determine its pathogenicity and name any linked disease? | Benign | TAGCATGATACTGACATTAAAAACAGACACATAGACCAATGGAACAGAATAGAGAACCCAGACACAAATACACACACCTAAAGTGAACTCATTTTTCACAAAGATGCCAAGAACATACACTAGGGAAAAGACATTCTCTTCAATAAATGGCACTGGGAAAACTGGATATCTATCCGCAGAACAATGAAACTAGACTCCTAACTCTTGTCACATATAAAAATCAAACGAAAATGGGTTAAAGACTCAAATCTAAGACTTCACACTGTGAAACTACTACAAGTAAACATTGGGTAAGATCTCCAGGACATTGATCTGAGCAA... | TAGCATGATACTGACATTAAAAACAGACACATAGACCAATGGAACAGAATAGAGAACCCAGACACAAATACACACACCTAAAGTGAACTCATTTTTCACAAAGATGCCAAGAACATACACTAGGGAAAAGACATTCTCTTCAATAAATGGCACTGGGAAAACTGGATATCTATCCGCAGAACAATGAAACTAGACTCCTAACTCTTGTCACATATAAAAATCAAACGAAAATGGGTTAAAGACTCAAATCTAAGACTTCACACTGTGAAACTACTACAAGTAAACATTGGGTAAGATCTCCAGGACATTGATCTGAGCAA... |
Task1_train_45201 | A variant on Chromosome 17 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | CAGCAATTCTACTCCTAAGTATTGACCCAAAAGAAAGGAAATCAGTATATCCAAGAGACATCTGCACTCCTATGTTTCCTGCAGCACTGTTTAAAATAGCTAAGATTTGGAAGCACTCTAAGCGTCCATCAGCAGATGAATGGATAAAGAAAATGATGTGCATATACACAATGGAGTACTATTCAGCCATAGAAAAGAATGAGATCCAATCACTTGCAACAACACGAATGGAACTTGAAATCATTACGTTAAATGAAATAAGCCAGGCAGAGAAAGACAAACATCACATGTTCTCACTTATTTGTGGCATCTAAAAATCA... | CAGCAATTCTACTCCTAAGTATTGACCCAAAAGAAAGGAAATCAGTATATCCAAGAGACATCTGCACTCCTATGTTTCCTGCAGCACTGTTTAAAATAGCTAAGATTTGGAAGCACTCTAAGCGTCCATCAGCAGATGAATGGATAAAGAAAATGATGTGCATATACACAATGGAGTACTATTCAGCCATAGAAAAGAATGAGATCCAATCACTTGCAACAACACGAATGGAACTTGAAATCATTACGTTAAATGAAATAAGCCAGGCAGAGAAAGACAAACATCACATGTTCTCACTTATTTGTGGCATCTAAAAATCA... |
Task1_train_45202 | A variant on Chromosome 17 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TCTGTTTTCCAAAAAAAAATTAATGTTAGATATTGTGGTTAGATTCTTAGGTCAGATACAAATTGCAAAATTAACTTTTGATGCCACTGACACACTATATTTCAAATGAAAATTAACAGTAAAAATGCATTAATAGTAATTTAATACATTACCATATAATTGGGTTTATTTTTAAAGCAGTTAAAATGAGACGTGATGGCTAGTGAAGGAAAGCTGACTTTTGTGCAGATTCTGAGGAAGAAGCTTACATTTTCAGACATTTTATAAGCTGCTAGTACTGGTCCAATTGCTAGTACTGGTCCAATTTCATTTGAGGCTTT... | TCTGTTTTCCAAAAAAAAATTAATGTTAGATATTGTGGTTAGATTCTTAGGTCAGATACAAATTGCAAAATTAACTTTTGATGCCACTGACACACTATATTTCAAATGAAAATTAACAGTAAAAATGCATTAATAGTAATTTAATACATTACCATATAATTGGGTTTATTTTTAAAGCAGTTAAAATGAGACGTGATGGCTAGTGAAGGAAAGCTGACTTTTGTGCAGATTCTGAGGAAGAAGCTTACATTTTCAGACATTTTATAAGCTGCTAGTACTGGTCCAATTGCTAGTACTGGTCCAATTTCATTTGAGGCTTT... |
Task1_train_45203 | Here is a variant on Chromosome 17. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CAGTGAAGGTTGGGGCTTCAACATGGGAATTTAGGGGTGAGGATGGGACACAAACATTCAGTCCATAACAATGGCCCACCAAACTATGAAAGCAAATAGAAAAAAAAATCACAGTTCAAGAATGACATAAAACTTAAGTAGTTATGCTATAGAGTAATGCATACAGCTACGCTGAGATGTTACAATGTAACAACATAAACTCACTGCATTTTTTTTCTTCTTCTTCTTTTTGAGACAGTCTCACTCTGTTGCCCAGGCTGGAGTACAGTGACATGATCTCAGCTCACTGCAACCTCTGCCTCCAGGATTCAAGTGATTCT... | CAGTGAAGGTTGGGGCTTCAACATGGGAATTTAGGGGTGAGGATGGGACACAAACATTCAGTCCATAACAATGGCCCACCAAACTATGAAAGCAAATAGAAAAAAAAATCACAGTTCAAGAATGACATAAAACTTAAGTAGTTATGCTATAGAGTAATGCATACAGCTACGCTGAGATGTTACAATGTAACAACATAAACTCACTGCATTTTTTTTCTTCTTCTTCTTTTTGAGACAGTCTCACTCTGTTGCCCAGGCTGGAGTACAGTGACATGATCTCAGCTCACTGCAACCTCTGCCTCCAGGATTCAAGTGATTCT... |
Task1_train_45204 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | ACATGGGAATTTAGGGGTGAGGATGGGACACAAACATTCAGTCCATAACAATGGCCCACCAAACTATGAAAGCAAATAGAAAAAAAAATCACAGTTCAAGAATGACATAAAACTTAAGTAGTTATGCTATAGAGTAATGCATACAGCTACGCTGAGATGTTACAATGTAACAACATAAACTCACTGCATTTTTTTTCTTCTTCTTCTTTTTGAGACAGTCTCACTCTGTTGCCCAGGCTGGAGTACAGTGACATGATCTCAGCTCACTGCAACCTCTGCCTCCAGGATTCAAGTGATTCTCATGCTTCAGCCTCCCAAGT... | ACATGGGAATTTAGGGGTGAGGATGGGACACAAACATTCAGTCCATAACAATGGCCCACCAAACTATGAAAGCAAATAGAAAAAAAAATCACAGTTCAAGAATGACATAAAACTTAAGTAGTTATGCTATAGAGTAATGCATACAGCTACGCTGAGATGTTACAATGTAACAACATAAACTCACTGCATTTTTTTTCTTCTTCTTCTTTTTGAGACAGTCTCACTCTGTTGCCCAGGCTGGAGTACAGTGACATGATCTCAGCTCACTGCAACCTCTGCCTCCAGGATTCAAGTGATTCTCATGCTTCAGCCTCCCAAGT... |
Task1_train_45205 | This variant is present on Chromosome 17. Is the change likely to result in a pathogenic outcome? | Benign | ACAAACATTCAGTCCATAACAATGGCCCACCAAACTATGAAAGCAAATAGAAAAAAAAATCACAGTTCAAGAATGACATAAAACTTAAGTAGTTATGCTATAGAGTAATGCATACAGCTACGCTGAGATGTTACAATGTAACAACATAAACTCACTGCATTTTTTTTCTTCTTCTTCTTTTTGAGACAGTCTCACTCTGTTGCCCAGGCTGGAGTACAGTGACATGATCTCAGCTCACTGCAACCTCTGCCTCCAGGATTCAAGTGATTCTCATGCTTCAGCCTCCCAAGTAGCTGGGATACAGGCATGCACCACCATGC... | ACAAACATTCAGTCCATAACAATGGCCCACCAAACTATGAAAGCAAATAGAAAAAAAAATCACAGTTCAAGAATGACATAAAACTTAAGTAGTTATGCTATAGAGTAATGCATACAGCTACGCTGAGATGTTACAATGTAACAACATAAACTCACTGCATTTTTTTTCTTCTTCTTCTTTTTGAGACAGTCTCACTCTGTTGCCCAGGCTGGAGTACAGTGACATGATCTCAGCTCACTGCAACCTCTGCCTCCAGGATTCAAGTGATTCTCATGCTTCAGCCTCCCAAGTAGCTGGGATACAGGCATGCACCACCATGC... |
Task1_train_45206 | A variant found on Chromosome 17 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | AACTTCTACTGAAAGCCAGCATTTTCTCTTGGCCTATAATTTCTCTGTAAAGGTACCATTAATGTTCACTATTACAATTAAGCCTTGGTCTGGGTTATTCTGATAACAAACTCTGGAGATCACAATTTTAAGGATTAAATAATCATAACAATATTGTTTGTTCTGCCGAAATGATTAATCTGACAGTGACTGAATTATCTTGGGACTCTCCCAAGCCCTAAATGAATACAGCAAAGATAAATTCAGGAAACAACTGCTTCTCCTATGGCCTGTAAGCTCCTAACAGACCATGCTTCTGCAGAAAACAATTCTGGACAAAT... | AACTTCTACTGAAAGCCAGCATTTTCTCTTGGCCTATAATTTCTCTGTAAAGGTACCATTAATGTTCACTATTACAATTAAGCCTTGGTCTGGGTTATTCTGATAACAAACTCTGGAGATCACAATTTTAAGGATTAAATAATCATAACAATATTGTTTGTTCTGCCGAAATGATTAATCTGACAGTGACTGAATTATCTTGGGACTCTCCCAAGCCCTAAATGAATACAGCAAAGATAAATTCAGGAAACAACTGCTTCTCCTATGGCCTGTAAGCTCCTAACAGACCATGCTTCTGCAGAAAACAATTCTGGACAAAT... |
Task1_train_45207 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | TGGGCCAGATGATTTCTAAAGGCACCTGAAACTCATCCCCAAGAGGCTTGTGGCATTGTCACTGTGTACACCTGGATCTGCAGGACACAATCTTTCATGGATTTGTTTTCCACGAAATGTATTAAATGACTTCCTTCTCTCCTGATGTAAAAACTGGCAGTCAGTACCTGGAAATAAATGTTGTTGTAGATCAGCTTTGTGTTCCAGACCTTTCTTAGAATACACTGGTCTGCAAAGTGAAGGACTGTCAGATAGACTCAACTGAGACTCAAAGGCCTCAGCAAAGTCTGGAGGAAACTCTGAAAGAAAGAACATTTTAA... | TGGGCCAGATGATTTCTAAAGGCACCTGAAACTCATCCCCAAGAGGCTTGTGGCATTGTCACTGTGTACACCTGGATCTGCAGGACACAATCTTTCATGGATTTGTTTTCCACGAAATGTATTAAATGACTTCCTTCTCTCCTGATGTAAAAACTGGCAGTCAGTACCTGGAAATAAATGTTGTTGTAGATCAGCTTTGTGTTCCAGACCTTTCTTAGAATACACTGGTCTGCAAAGTGAAGGACTGTCAGATAGACTCAACTGAGACTCAAAGGCCTCAGCAAAGTCTGGAGGAAACTCTGAAAGAAAGAACATTTTAA... |
Task1_train_45208 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | ATCTACAAATAAAGACAATTTGACTTCCTCTCTTCCTATTCGAATACCTTTATTTCTTTCTCTTGCCTGATTGCCCTGGCCGGAACTTCCAATACTATGTTGAATAGGAGTGGTGAGAGAGGGCATTCTTGTCTTGTGCCAATTTTCAAAGGGAATGCTTCCAGGTTTTGCCCATTCAGTATGATATTGGCTGTGGGTTTGTCATGAATAGCTCTTATTGTTTTGAGATATGTTTCATCAATACCCAGTTTATTGAGAGTTTTTAACATAAAGGGATGTTGAATTTTGTCAGAGTCTTTTTCTGCATCTATTGAGATAAT... | ATCTACAAATAAAGACAATTTGACTTCCTCTCTTCCTATTCGAATACCTTTATTTCTTTCTCTTGCCTGATTGCCCTGGCCGGAACTTCCAATACTATGTTGAATAGGAGTGGTGAGAGAGGGCATTCTTGTCTTGTGCCAATTTTCAAAGGGAATGCTTCCAGGTTTTGCCCATTCAGTATGATATTGGCTGTGGGTTTGTCATGAATAGCTCTTATTGTTTTGAGATATGTTTCATCAATACCCAGTTTATTGAGAGTTTTTAACATAAAGGGATGTTGAATTTTGTCAGAGTCTTTTTCTGCATCTATTGAGATAAT... |
Task1_train_45209 | This sequence variant lies on Chromosome 17. Is it clinically significant, and what condition might it cause if any? | Benign | AGATTTTCCATATCACAGCATGGGTAAATAGAGCCCATGCAGAAATCAGCAGTTTTACTGGGCTAAAGAAAACAGAGGTCAGACTTCAGGGCTGCCAGAGGAGCTGGGATTTCAGAAACAAAATCCCAGAGAAGATGAAACTGAAGAGAAGAAGCCAAAATCTACCCACAAATTTCCCTCAACTCACTGGCTAATACAGGTGAGATGCTAGAAACACAGAAGAAAATATCAACTAGGGCTGGGTGTGGTGGCTTATGCCTGTAATCCCAGCAGTTTAGGAGGCCGAGGCAGGTGGATTGCTTGAGCCCAGGAGTTTGAGA... | AGATTTTCCATATCACAGCATGGGTAAATAGAGCCCATGCAGAAATCAGCAGTTTTACTGGGCTAAAGAAAACAGAGGTCAGACTTCAGGGCTGCCAGAGGAGCTGGGATTTCAGAAACAAAATCCCAGAGAAGATGAAACTGAAGAGAAGAAGCCAAAATCTACCCACAAATTTCCCTCAACTCACTGGCTAATACAGGTGAGATGCTAGAAACACAGAAGAAAATATCAACTAGGGCTGGGTGTGGTGGCTTATGCCTGTAATCCCAGCAGTTTAGGAGGCCGAGGCAGGTGGATTGCTTGAGCCCAGGAGTTTGAGA... |
Task1_train_45210 | A mutation found on Chromosome 17 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GAGCCCATGCAGAAATCAGCAGTTTTACTGGGCTAAAGAAAACAGAGGTCAGACTTCAGGGCTGCCAGAGGAGCTGGGATTTCAGAAACAAAATCCCAGAGAAGATGAAACTGAAGAGAAGAAGCCAAAATCTACCCACAAATTTCCCTCAACTCACTGGCTAATACAGGTGAGATGCTAGAAACACAGAAGAAAATATCAACTAGGGCTGGGTGTGGTGGCTTATGCCTGTAATCCCAGCAGTTTAGGAGGCCGAGGCAGGTGGATTGCTTGAGCCCAGGAGTTTGAGACCAGCCTGGGCAATATGGTGAAACCCTGTC... | GAGCCCATGCAGAAATCAGCAGTTTTACTGGGCTAAAGAAAACAGAGGTCAGACTTCAGGGCTGCCAGAGGAGCTGGGATTTCAGAAACAAAATCCCAGAGAAGATGAAACTGAAGAGAAGAAGCCAAAATCTACCCACAAATTTCCCTCAACTCACTGGCTAATACAGGTGAGATGCTAGAAACACAGAAGAAAATATCAACTAGGGCTGGGTGTGGTGGCTTATGCCTGTAATCCCAGCAGTTTAGGAGGCCGAGGCAGGTGGATTGCTTGAGCCCAGGAGTTTGAGACCAGCCTGGGCAATATGGTGAAACCCTGTC... |
Task1_train_45211 | A genomic variant on Chromosome 17 is under review. What is the biological outcome — benign or pathogenic? | Benign | TCATACATCTCCCTACATCAGAATGTCAATGCACTGGCATCTTTTGCAAAACCGATTGCTGAACTTCATTTCCTCCTATCCAAAACTACCCTAAAGCCCCCAAGGAAAGGTAAAAAGGAAGAAACACCAGGTAATTAGAGCAGTAGGAAGCAAGGGAGAGGTTTTTCTTTTCAACCCGTGCCTAGGTACAGACTAGCCCTTCTAATGGGCCTAAGCAATTCAGAAAGGCAGCTAAGAGAGCTTCTCGAAACCCTGCCTGCTCTTCCACCTCTTGGAAGGCTGAGGGGCTTTATCTAAAATCATAACCAAAATTTCCACAT... | TCATACATCTCCCTACATCAGAATGTCAATGCACTGGCATCTTTTGCAAAACCGATTGCTGAACTTCATTTCCTCCTATCCAAAACTACCCTAAAGCCCCCAAGGAAAGGTAAAAAGGAAGAAACACCAGGTAATTAGAGCAGTAGGAAGCAAGGGAGAGGTTTTTCTTTTCAACCCGTGCCTAGGTACAGACTAGCCCTTCTAATGGGCCTAAGCAATTCAGAAAGGCAGCTAAGAGAGCTTCTCGAAACCCTGCCTGCTCTTCCACCTCTTGGAAGGCTGAGGGGCTTTATCTAAAATCATAACCAAAATTTCCACAT... |
Task1_train_45212 | This sequence variant lies on Chromosome 17. Is it clinically significant, and what condition might it cause if any? | Benign | ATGTCAATGCACTGGCATCTTTTGCAAAACCGATTGCTGAACTTCATTTCCTCCTATCCAAAACTACCCTAAAGCCCCCAAGGAAAGGTAAAAAGGAAGAAACACCAGGTAATTAGAGCAGTAGGAAGCAAGGGAGAGGTTTTTCTTTTCAACCCGTGCCTAGGTACAGACTAGCCCTTCTAATGGGCCTAAGCAATTCAGAAAGGCAGCTAAGAGAGCTTCTCGAAACCCTGCCTGCTCTTCCACCTCTTGGAAGGCTGAGGGGCTTTATCTAAAATCATAACCAAAATTTCCACATGTCTCCTGGATTCAAGCCTCCC... | ATGTCAATGCACTGGCATCTTTTGCAAAACCGATTGCTGAACTTCATTTCCTCCTATCCAAAACTACCCTAAAGCCCCCAAGGAAAGGTAAAAAGGAAGAAACACCAGGTAATTAGAGCAGTAGGAAGCAAGGGAGAGGTTTTTCTTTTCAACCCGTGCCTAGGTACAGACTAGCCCTTCTAATGGGCCTAAGCAATTCAGAAAGGCAGCTAAGAGAGCTTCTCGAAACCCTGCCTGCTCTTCCACCTCTTGGAAGGCTGAGGGGCTTTATCTAAAATCATAACCAAAATTTCCACATGTCTCCTGGATTCAAGCCTCCC... |
Task1_train_45213 | A mutation on Chromosome 17 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | TTTGAATGGCTCTTCAGAATCTATATGCTTCCTCTCATTCTTAGCGCCCCCTATGACCATCTACACTGAACAAGATTTATACAATCATGTCGTACCTAAGCCCCGCAACAAAAGGGTACCCATTCTTCCTTTTGTTATCGGAGCAGGAGTGCTAGGTGGAGTAGGTACTGGCACTGGCGGTATCACAACCTCTATTCAGTTCTACTACAAACTATCTCAAGAACTAAATGGTGACATGGAACGGGTCTCTGACTCCCTGGTCACCTTGCAAGATCAACTTAACTCCCTAGCAGCAGTAGTCGTTCAAAATAGAAGAGCTT... | TTTGAATGGCTCTTCAGAATCTATATGCTTCCTCTCATTCTTAGCGCCCCCTATGACCATCTACACTGAACAAGATTTATACAATCATGTCGTACCTAAGCCCCGCAACAAAAGGGTACCCATTCTTCCTTTTGTTATCGGAGCAGGAGTGCTAGGTGGAGTAGGTACTGGCACTGGCGGTATCACAACCTCTATTCAGTTCTACTACAAACTATCTCAAGAACTAAATGGTGACATGGAACGGGTCTCTGACTCCCTGGTCACCTTGCAAGATCAACTTAACTCCCTAGCAGCAGTAGTCGTTCAAAATAGAAGAGCTT... |
Task1_train_45214 | The following genetic variant occurs on Chromosome 17. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | GTTTTCACTCTATTAAATCTTGCAACTGCAAAAAGAATATATATATATGTGTATATATATACACATATATATACATATATATATACACATATATATACACATATATATACACATATATATATACACATACATATTTTTGTGTGTGTGTAGTTGGTAAAACTCTTACGTCACAAAATCCTTTAGGGAGTCGCTTTCACAAACATAGAGGATCTCTTTTGGTTTGCAGTGAAACAAGTCCTTAATTTTCTCCATGATCTTTATGGCTAGGGCTGTCTTCCTGACTCCTGGAAAGCAGTAGATGAATAATTCACGTGTCTTCT... | GTTTTCACTCTATTAAATCTTGCAACTGCAAAAAGAATATATATATATGTGTATATATATACACATATATATACATATATATATACACATATATATACACATATATATACACATATATATATACACATACATATTTTTGTGTGTGTGTAGTTGGTAAAACTCTTACGTCACAAAATCCTTTAGGGAGTCGCTTTCACAAACATAGAGGATCTCTTTTGGTTTGCAGTGAAACAAGTCCTTAATTTTCTCCATGATCTTTATGGCTAGGGCTGTCTTCCTGACTCCTGGAAAGCAGTAGATGAATAATTCACGTGTCTTCT... |
Task1_train_45215 | A mutation has occurred on Chromosome 17. What is the medical relevance of this mutation? | Benign | CATATATATACACATATATATACACATATATATATACACATACATATTTTTGTGTGTGTGTAGTTGGTAAAACTCTTACGTCACAAAATCCTTTAGGGAGTCGCTTTCACAAACATAGAGGATCTCTTTTGGTTTGCAGTGAAACAAGTCCTTAATTTTCTCCATGATCTTTATGGCTAGGGCTGTCTTCCTGACTCCTGGAAAGCAGTAGATGAATAATTCACGTGTCTTCTGAAGACTCTCAGAAAGCAACTGGCTCTGCTCCATTATGAGCAAGTTGAAAAATTCACAGCCCATCTGGTCACTCAGAAGAGATCTGG... | CATATATATACACATATATATACACATATATATATACACATACATATTTTTGTGTGTGTGTAGTTGGTAAAACTCTTACGTCACAAAATCCTTTAGGGAGTCGCTTTCACAAACATAGAGGATCTCTTTTGGTTTGCAGTGAAACAAGTCCTTAATTTTCTCCATGATCTTTATGGCTAGGGCTGTCTTCCTGACTCCTGGAAAGCAGTAGATGAATAATTCACGTGTCTTCTGAAGACTCTCAGAAAGCAACTGGCTCTGCTCCATTATGAGCAAGTTGAAAAATTCACAGCCCATCTGGTCACTCAGAAGAGATCTGG... |
Task1_train_45216 | A mutation on Chromosome 17 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | GAAGGCAAGCAGATAGGCGTAGTTCGGCCTATAGTCCTTTATGGATTGATTAGGAATCACCAAGGCTGATTCCAATCAAAACTGAAAGGTAAGTGAGAACACCAGGGGTCCTGCTCCCCCCAGCACCCCCTTGCCCTAGCATCTCCTTTTGCATCATTTTCCCCCACTTGGTGGTGCCCTAAGCCCAGTGGCTTAAGGTTATTAGCTCCTAATGTTACTGAAACAATTCAAATTTGTCAACAATGTTTTGCTTGAAAGAATTAGTGGAGTAGTGGAGTCATTTATTTTTATTTTTTTATTTTTATTTATTTATTTTTTTG... | GAAGGCAAGCAGATAGGCGTAGTTCGGCCTATAGTCCTTTATGGATTGATTAGGAATCACCAAGGCTGATTCCAATCAAAACTGAAAGGTAAGTGAGAACACCAGGGGTCCTGCTCCCCCCAGCACCCCCTTGCCCTAGCATCTCCTTTTGCATCATTTTCCCCCACTTGGTGGTGCCCTAAGCCCAGTGGCTTAAGGTTATTAGCTCCTAATGTTACTGAAACAATTCAAATTTGTCAACAATGTTTTGCTTGAAAGAATTAGTGGAGTAGTGGAGTCATTTATTTTTATTTTTTTATTTTTATTTATTTATTTTTTTG... |
Task1_train_45217 | With a mutation on Chromosome 17, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TAAAAATCAGGGAGTGTTTTCCCTCGTTTCTGTACCAAGGTGTTGGCTCCATTCCTCATGGTAGGAGGGGAGGGGTCCCCACAGGGCTTGCCTGCTGAGCTCCGTGTGGAAGGAGGGTGAAGGTGGTGAGGTGGCCCCCAGTCCCAAAGCCCAGGTCAACAGGGAGACCACCGGTGAAGAGTTTGGGATTTATCACCTTTCCACCTAACCCCAAACCCTCCAGCTAATTCCAACCATTCAGAAGGGAAGCAGAACTTCTCCCCTGCCACTGTCTGGAAAATTTCCATAATGGGACTCAATCCCAGCTTCTCCGTCTGCGT... | TAAAAATCAGGGAGTGTTTTCCCTCGTTTCTGTACCAAGGTGTTGGCTCCATTCCTCATGGTAGGAGGGGAGGGGTCCCCACAGGGCTTGCCTGCTGAGCTCCGTGTGGAAGGAGGGTGAAGGTGGTGAGGTGGCCCCCAGTCCCAAAGCCCAGGTCAACAGGGAGACCACCGGTGAAGAGTTTGGGATTTATCACCTTTCCACCTAACCCCAAACCCTCCAGCTAATTCCAACCATTCAGAAGGGAAGCAGAACTTCTCCCCTGCCACTGTCTGGAAAATTTCCATAATGGGACTCAATCCCAGCTTCTCCGTCTGCGT... |
Task1_train_45218 | A mutation located on Chromosome 17 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | AGACTTTACAGCCTCTCAGTCATAACTTCTTGGATGTAGATGTGTTAGGAACACTTTCAGCCACCCGTCTTGTCCCTGAGTGATCTCAGGTCCCAAACTCCAGAGCAAAGCTTTGAAATCTTGGGCAAGGGTGCCTTGTGGGAGCCTGTGTGTTGAGGGCAGGACTGGTCTCTGTCCGTGGTGCTGACCCACCAGCCACTTCCAGGAAAGATGGGGCTGCCTGGCAAGGTTGGCTGAGCCTCAAAAGAGGAAGCCTCTCTCACCACCAACTCCTTCCTTCTAGTCCCCATCTCCTCCAGTGGGATAACATCTGAAGCTAT... | AGACTTTACAGCCTCTCAGTCATAACTTCTTGGATGTAGATGTGTTAGGAACACTTTCAGCCACCCGTCTTGTCCCTGAGTGATCTCAGGTCCCAAACTCCAGAGCAAAGCTTTGAAATCTTGGGCAAGGGTGCCTTGTGGGAGCCTGTGTGTTGAGGGCAGGACTGGTCTCTGTCCGTGGTGCTGACCCACCAGCCACTTCCAGGAAAGATGGGGCTGCCTGGCAAGGTTGGCTGAGCCTCAAAAGAGGAAGCCTCTCTCACCACCAACTCCTTCCTTCTAGTCCCCATCTCCTCCAGTGGGATAACATCTGAAGCTAT... |
Task1_train_45219 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | CCCACAACTGGTCAAGGGATCCCAAAGCCTGCCCCCAGAGCGCTCCTTTTGCTGTAAACGGTTTTGCATCTGTACATGCCTGTACCCAAAACAGGGCCCTAATGCCACTGGCTTTGCCCCTGTGGCCTGTGTGGAGAGCCCATGGGAGTCCTGGTCCCACTCCACCCTCAGGCAAGTCACATGTCTCTTCAAGCTTCAGCTTCCTGTGTTGGGAAGTGGGGCCACAGGTTCTTGCCCCTATCTGCATCACAGGGCTACTGCCTCAGGTCTAGGGGAGGGCCCAGAGAGCTGGCTCTGCTCCCAGGTTTGGCCTGTGCCCA... | CCCACAACTGGTCAAGGGATCCCAAAGCCTGCCCCCAGAGCGCTCCTTTTGCTGTAAACGGTTTTGCATCTGTACATGCCTGTACCCAAAACAGGGCCCTAATGCCACTGGCTTTGCCCCTGTGGCCTGTGTGGAGAGCCCATGGGAGTCCTGGTCCCACTCCACCCTCAGGCAAGTCACATGTCTCTTCAAGCTTCAGCTTCCTGTGTTGGGAAGTGGGGCCACAGGTTCTTGCCCCTATCTGCATCACAGGGCTACTGCCTCAGGTCTAGGGGAGGGCCCAGAGAGCTGGCTCTGCTCCCAGGTTTGGCCTGTGCCCA... |
Task1_train_45220 | With a mutation on Chromosome 17, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | ATACACTCAAAATAGTGAAACCACCCTTGGTTTTTACTTACAGCTCGCTCACAGGCAAAACATGAATCTAGAAGTGATGGGGTAGGTTGGGAGATAATTCTGAGTGACACACTATACAGGTTTAGTATCCCTTATCCAAAATGCTTGGAACCAAAAATGTTTTGGATTTCAGATTTTTTTTTCAGAGTTTGGAGTATTTACATTATACTTACAGGTTGAATATCTCTAATCCCCAAATCCAAAATGCTGCAATGAGCATTTTCTTTGAGTGTCATGTTGGTATTGAAAAAGTTTCTAGTTGGAGCATTTTGGATTTTGGG... | ATACACTCAAAATAGTGAAACCACCCTTGGTTTTTACTTACAGCTCGCTCACAGGCAAAACATGAATCTAGAAGTGATGGGGTAGGTTGGGAGATAATTCTGAGTGACACACTATACAGGTTTAGTATCCCTTATCCAAAATGCTTGGAACCAAAAATGTTTTGGATTTCAGATTTTTTTTTCAGAGTTTGGAGTATTTACATTATACTTACAGGTTGAATATCTCTAATCCCCAAATCCAAAATGCTGCAATGAGCATTTTCTTTGAGTGTCATGTTGGTATTGAAAAAGTTTCTAGTTGGAGCATTTTGGATTTTGGG... |
Task1_train_45221 | A variant was discovered on Chromosome 17. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | GTCTCTAATAAAAATACAACCACAAGAAAATAGCCAGGTGTGGTGGTAGGCACCTGTAACCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGATGGAGGTTGCTGTGAGCCGAGATCACGCCAGTGCACTTCAGCCTGGGCGACTGAGTGAGGCTCCATCTCAAAAAAGAAAAAACTTTGGTACAGATAATCTGGCTCCTCCCTGGGCATCACCCCCGGGAGCCTACTCCACTCCATTAGCCTACAGCCCTGCCTCTGACTTCAAACCCTAAGCATGATGGCCATGAATACTAAAAAAATACTC... | GTCTCTAATAAAAATACAACCACAAGAAAATAGCCAGGTGTGGTGGTAGGCACCTGTAACCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGATGGAGGTTGCTGTGAGCCGAGATCACGCCAGTGCACTTCAGCCTGGGCGACTGAGTGAGGCTCCATCTCAAAAAAGAAAAAACTTTGGTACAGATAATCTGGCTCCTCCCTGGGCATCACCCCCGGGAGCCTACTCCACTCCATTAGCCTACAGCCCTGCCTCTGACTTCAAACCCTAAGCATGATGGCCATGAATACTAAAAAAATACTC... |
Task1_train_45222 | A mutation is present on Chromosome 17. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | ATTCCTCTCATAGTTAGCTTGGCCTGTGCCCAGGAATGAGCAAGGGCAGCTTGGAGGTTAGAAGCAAAATGGAATCAGTTAGGTCAGATTTGTCATAATTTTTATAAAGGCAGTTTCAGTAACACAAGAAGTAAAGTGAGTCCTACTACTGTTTATTTTAATCCTAGAATGTCAGAGCCAGAAGAGACCCTACAGGACAAGTCTCTTGTGATTTCTGAATAATGATCCTCAGACTCATGCTGTGATAAAGTTTTCACCCCTACTCTACAAAATGAGGACCATATGGAAAATATAATCAGGTTTTTTATAATTTCATAAAA... | ATTCCTCTCATAGTTAGCTTGGCCTGTGCCCAGGAATGAGCAAGGGCAGCTTGGAGGTTAGAAGCAAAATGGAATCAGTTAGGTCAGATTTGTCATAATTTTTATAAAGGCAGTTTCAGTAACACAAGAAGTAAAGTGAGTCCTACTACTGTTTATTTTAATCCTAGAATGTCAGAGCCAGAAGAGACCCTACAGGACAAGTCTCTTGTGATTTCTGAATAATGATCCTCAGACTCATGCTGTGATAAAGTTTTCACCCCTACTCTACAAAATGAGGACCATATGGAAAATATAATCAGGTTTTTTATAATTTCATAAAA... |
Task1_train_45223 | This is a variant located on Chromosome 17. Is this mutation a likely cause of disease or not? | Benign | GTTAGAGGAGACCAATGATAGCTTGACTGGTAATGAAGTGCATAAGATGAATCCCTTTGGGGGACATACATTTAGAACCCTCAGCCTCTGAGCTGAGTGTCAACTACAAATGACTTAGTTATTCACACTTGCCAAGGAACCGGGAGGAAGCTGGCTCATTCTTTTGTTTATTGGTGACTTGATCGGGCAAACATGTGTTGAGCTAGTATTATATGCTGGGCTCTATGGGGGTAAAAACATGAGGAAGATACAGTCACTACCCTTAAGTAACTTACAGACTAGTCAGGGTTGAAAGAGAAATTGAAAAGTTAAACAAACAC... | GTTAGAGGAGACCAATGATAGCTTGACTGGTAATGAAGTGCATAAGATGAATCCCTTTGGGGGACATACATTTAGAACCCTCAGCCTCTGAGCTGAGTGTCAACTACAAATGACTTAGTTATTCACACTTGCCAAGGAACCGGGAGGAAGCTGGCTCATTCTTTTGTTTATTGGTGACTTGATCGGGCAAACATGTGTTGAGCTAGTATTATATGCTGGGCTCTATGGGGGTAAAAACATGAGGAAGATACAGTCACTACCCTTAAGTAACTTACAGACTAGTCAGGGTTGAAAGAGAAATTGAAAAGTTAAACAAACAC... |
Task1_train_45224 | Here’s a variant located on Chromosome 17. What is the predicted biological effect — harmless or disease-causing? | Benign | TGTGTTTGCTACAGAAAAATTGCTGTGTTTGATTGAAATAGTCTTCCTTGGCCCCACCAAGGATAAGTACCATCTAGGTATGTATTACTTTTTTTTTTTTTTTTAATTGAGACAGGGTCTTTTTCTGTCACCCAGGCTGGGGCGCAGTGGTATGATCATAACTCACTGCAGCCTTGAGGTCCTGGGCTCAAGTGATCCTCCTGCCTCAGCCTCCTGAGAAGCTGGAACTACAGGTGCGAGCCACAATGCCTAGCTAATAGTTTACCTTTTTGTAGTGATGAGGTCTTGCTATGATGCCCAGGCTGGTCTTGAACTCCTGT... | TGTGTTTGCTACAGAAAAATTGCTGTGTTTGATTGAAATAGTCTTCCTTGGCCCCACCAAGGATAAGTACCATCTAGGTATGTATTACTTTTTTTTTTTTTTTTAATTGAGACAGGGTCTTTTTCTGTCACCCAGGCTGGGGCGCAGTGGTATGATCATAACTCACTGCAGCCTTGAGGTCCTGGGCTCAAGTGATCCTCCTGCCTCAGCCTCCTGAGAAGCTGGAACTACAGGTGCGAGCCACAATGCCTAGCTAATAGTTTACCTTTTTGTAGTGATGAGGTCTTGCTATGATGCCCAGGCTGGTCTTGAACTCCTGT... |
Task1_train_45225 | Here’s a variant located on Chromosome 17. What is the predicted biological effect — harmless or disease-causing? | Benign | CAGTACAGATAGGGAGACACAAGAAAGAGGCAGAAGCTTTAAGGGTCACCATGCAAACCCACAAACCCCAGAATTCCTAAGGTGCATCTGTTAACTCCTACAGATGTGGCAAGAACAGTTATCTCTCTTCTAAAATTTAACCACACCCATGCAAGTCTTAATTTCTTTCACTAAGGTGAAACAGCTCAGGGTACAATGTTGTTAGTATATTACACTTCCTATTTCGGTAATCTTTGGTGGCAAGAACAGTTATCTCTCTTCTAAAATTTAACCACACCCATACAAGTCTTAATTTCTTTCACCAGGGTGAAACAGCTCAG... | CAGTACAGATAGGGAGACACAAGAAAGAGGCAGAAGCTTTAAGGGTCACCATGCAAACCCACAAACCCCAGAATTCCTAAGGTGCATCTGTTAACTCCTACAGATGTGGCAAGAACAGTTATCTCTCTTCTAAAATTTAACCACACCCATGCAAGTCTTAATTTCTTTCACTAAGGTGAAACAGCTCAGGGTACAATGTTGTTAGTATATTACACTTCCTATTTCGGTAATCTTTGGTGGCAAGAACAGTTATCTCTCTTCTAAAATTTAACCACACCCATACAAGTCTTAATTTCTTTCACCAGGGTGAAACAGCTCAG... |
Task1_train_45226 | Chromosome 17 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | TGTAACACAGCTTTTCCAGTGCCTGGTACAAGGTAAGTGTCCAATAAGAAGTTACAAATGTTCCTGAGCCACCCTACTGGGTCCCTCCTCACATCCAATGCTGGACTCTTCATGCCCAAGGAAACATATAAGGCACAAAAGTCAGTGGCACTCAGCTCAGCAGAAGAAGGCACAGGAAGGGGATGGGGGAGTCCTGGCTCCCACTTTGTTCTTGGGGTCAGGCTTGTGGCCAGCCTGGAAAGACTGACATGAACCCTCCAGCATCTGAGGGTGCCAACCACCAAGAGCAGCACAGTTCTTGTCTACAAGCCACTTGTAGC... | TGTAACACAGCTTTTCCAGTGCCTGGTACAAGGTAAGTGTCCAATAAGAAGTTACAAATGTTCCTGAGCCACCCTACTGGGTCCCTCCTCACATCCAATGCTGGACTCTTCATGCCCAAGGAAACATATAAGGCACAAAAGTCAGTGGCACTCAGCTCAGCAGAAGAAGGCACAGGAAGGGGATGGGGGAGTCCTGGCTCCCACTTTGTTCTTGGGGTCAGGCTTGTGGCCAGCCTGGAAAGACTGACATGAACCCTCCAGCATCTGAGGGTGCCAACCACCAAGAGCAGCACAGTTCTTGTCTACAAGCCACTTGTAGC... |
Task1_train_45227 | A variant on Chromosome 17 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GTAACACAGCTTTTCCAGTGCCTGGTACAAGGTAAGTGTCCAATAAGAAGTTACAAATGTTCCTGAGCCACCCTACTGGGTCCCTCCTCACATCCAATGCTGGACTCTTCATGCCCAAGGAAACATATAAGGCACAAAAGTCAGTGGCACTCAGCTCAGCAGAAGAAGGCACAGGAAGGGGATGGGGGAGTCCTGGCTCCCACTTTGTTCTTGGGGTCAGGCTTGTGGCCAGCCTGGAAAGACTGACATGAACCCTCCAGCATCTGAGGGTGCCAACCACCAAGAGCAGCACAGTTCTTGTCTACAAGCCACTTGTAGCA... | GTAACACAGCTTTTCCAGTGCCTGGTACAAGGTAAGTGTCCAATAAGAAGTTACAAATGTTCCTGAGCCACCCTACTGGGTCCCTCCTCACATCCAATGCTGGACTCTTCATGCCCAAGGAAACATATAAGGCACAAAAGTCAGTGGCACTCAGCTCAGCAGAAGAAGGCACAGGAAGGGGATGGGGGAGTCCTGGCTCCCACTTTGTTCTTGGGGTCAGGCTTGTGGCCAGCCTGGAAAGACTGACATGAACCCTCCAGCATCTGAGGGTGCCAACCACCAAGAGCAGCACAGTTCTTGTCTACAAGCCACTTGTAGCA... |
Task1_train_45228 | Chromosome 17 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CCTCAAAGAAACGACAGTTAGCTATTTGATGTGTGTCTTTCCAAATATTTGCCTATGTAAATATATGTGTGTATATGGCTTTTAAAAATAAAAACAAAATAATATCCTTTACAGACAGTTTTGTAGCATATGTAGAGAATATATATGCATATACTGAATGTAAATAGATATGCATTTTACCTAGAATATTGAGGACACTTTCCACAGTTATAGATGTGTGCTGCTTTTGTTTACTGACTGCAGAATATTCCATTGATGGACATCTTAATCCTCTACTTATTAATCCCCTACTGATGACTGTTTGCATTTCTTTGCTCTTT... | CCTCAAAGAAACGACAGTTAGCTATTTGATGTGTGTCTTTCCAAATATTTGCCTATGTAAATATATGTGTGTATATGGCTTTTAAAAATAAAAACAAAATAATATCCTTTACAGACAGTTTTGTAGCATATGTAGAGAATATATATGCATATACTGAATGTAAATAGATATGCATTTTACCTAGAATATTGAGGACACTTTCCACAGTTATAGATGTGTGCTGCTTTTGTTTACTGACTGCAGAATATTCCATTGATGGACATCTTAATCCTCTACTTATTAATCCCCTACTGATGACTGTTTGCATTTCTTTGCTCTTT... |
Task1_train_45229 | A mutation is present on Chromosome 17. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CACCTGAGCCTACTGAGCAGCTGGGACTACAGGTGTGTATCACCACTCCCAGTCAAGTTTTTTTTTTGTATGTGTGTTTTTTATAGAGACAGTGTTTCACCATGTTCCCCAGGCTGGTCTCAAACTTCTGGGCTCAAGCAATCTGCCTGCCTTGACCTCCCAAAGTGCTGGGATTTCAGGTGTGAGGCCCTGTACCCAGCTCAATTCTGTTTTTATACTAGAAGAACATTCTCTATCTGGGTCTTCCAGACTTGATTCTTACTGGTTAATTTGTCCTGGTCTTTTGCTGGTCCAAGAAAATATCTTGAAATCTTTATTTC... | CACCTGAGCCTACTGAGCAGCTGGGACTACAGGTGTGTATCACCACTCCCAGTCAAGTTTTTTTTTTGTATGTGTGTTTTTTATAGAGACAGTGTTTCACCATGTTCCCCAGGCTGGTCTCAAACTTCTGGGCTCAAGCAATCTGCCTGCCTTGACCTCCCAAAGTGCTGGGATTTCAGGTGTGAGGCCCTGTACCCAGCTCAATTCTGTTTTTATACTAGAAGAACATTCTCTATCTGGGTCTTCCAGACTTGATTCTTACTGGTTAATTTGTCCTGGTCTTTTGCTGGTCCAAGAAAATATCTTGAAATCTTTATTTC... |
Task1_train_45230 | Chromosome 17 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | GAATCTTGATTCGAATCTTGATTCAAATCTTGGCAGTGCCATTCATCAGCTCTGTGGCATTGAGCGCCATCAGTGGACCACTCTCTGATCCCCAATTGCCTTATCTGTAAAATGAGATTAGACACCCCTGCTCAAGATTATGGTAGGATTATATATAATATGTGTAACACAGCTTTCCCAGTGCCTGGTACAAGGTAAGTGTCCAATAAGAACTTACAAATGTTCCTGAGCCACCCTACTGGGTCCCTCCGCACATCCAATGCTGGACTCTTCATGCCCAAGGAAACATATAGGGCACAAAAGTCAGTGGCACTGAGCTC... | GAATCTTGATTCGAATCTTGATTCAAATCTTGGCAGTGCCATTCATCAGCTCTGTGGCATTGAGCGCCATCAGTGGACCACTCTCTGATCCCCAATTGCCTTATCTGTAAAATGAGATTAGACACCCCTGCTCAAGATTATGGTAGGATTATATATAATATGTGTAACACAGCTTTCCCAGTGCCTGGTACAAGGTAAGTGTCCAATAAGAACTTACAAATGTTCCTGAGCCACCCTACTGGGTCCCTCCGCACATCCAATGCTGGACTCTTCATGCCCAAGGAAACATATAGGGCACAAAAGTCAGTGGCACTGAGCTC... |
Task1_train_45231 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | AGTGAAACTTTATCGATCCCTAGAGGGGAGAGAGAGATGCAGCTTTAGCACTAGTTCCTGGGAGTGCCAGGGCCTAACAACCCCACAGAGCAGACGCTAAAAATGCAAGAAGGTATGGACAAGTACTAGTATTGGGGGCCACAGCAGGATTAAAATAGCATTACATCCACTCAGTGTGAGACAGATGAGGAAACCCTAGGAGGAGGCGCTCCCTAAGAGGAATGTCTGTCACATTCCTATGACTGCTTAAAGCCAGAAGGGCAAAACATTTACCCTTCTGTTTAGCAGGCCTGTGTGTTTTCATGGGAGACTTCATCCAG... | AGTGAAACTTTATCGATCCCTAGAGGGGAGAGAGAGATGCAGCTTTAGCACTAGTTCCTGGGAGTGCCAGGGCCTAACAACCCCACAGAGCAGACGCTAAAAATGCAAGAAGGTATGGACAAGTACTAGTATTGGGGGCCACAGCAGGATTAAAATAGCATTACATCCACTCAGTGTGAGACAGATGAGGAAACCCTAGGAGGAGGCGCTCCCTAAGAGGAATGTCTGTCACATTCCTATGACTGCTTAAAGCCAGAAGGGCAAAACATTTACCCTTCTGTTTAGCAGGCCTGTGTGTTTTCATGGGAGACTTCATCCAG... |
Task1_train_45232 | This variant lies on Chromosome 17. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | CACAAGGCTCAGAGGTCCCTTCCGAGAGCCCACGGCAGGTATGGGGGCAAAAGATGCCGTAAACATAGCCCTGGATGTCTCCAACCTGATGCAAAAGAACCTTGCTCTAGGGAAACCTGCAGTCTGGTGAAAAAAGGACAACTCCTGCCCAGGGAGTCCGTCGTCTTGACGTGGGAGGCATACCCATCACCTAAGGATGCTCCGATTTTGAGAGAAAGGGAGATATCCTATCCATGCCTTGGGGGACTCCCAGTCCGATGGAAAAGGCACAACTCTAGGGAAGCCCTTGTTCTGTTAGCGACAGATGCCATTCTAGGAGA... | CACAAGGCTCAGAGGTCCCTTCCGAGAGCCCACGGCAGGTATGGGGGCAAAAGATGCCGTAAACATAGCCCTGGATGTCTCCAACCTGATGCAAAAGAACCTTGCTCTAGGGAAACCTGCAGTCTGGTGAAAAAAGGACAACTCCTGCCCAGGGAGTCCGTCGTCTTGACGTGGGAGGCATACCCATCACCTAAGGATGCTCCGATTTTGAGAGAAAGGGAGATATCCTATCCATGCCTTGGGGGACTCCCAGTCCGATGGAAAAGGCACAACTCTAGGGAAGCCCTTGTTCTGTTAGCGACAGATGCCATTCTAGGAGA... |
Task1_train_45233 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | AAAAGAACCTTGCTCTAGGGAAACCTGCAGTCTGGTGAAAAAAGGACAACTCCTGCCCAGGGAGTCCGTCGTCTTGACGTGGGAGGCATACCCATCACCTAAGGATGCTCCGATTTTGAGAGAAAGGGAGATATCCTATCCATGCCTTGGGGGACTCCCAGTCCGATGGAAAAGGCACAACTCTAGGGAAGCCCTTGTTCTGTTAGCGACAGATGCCATTCTAGGAGAGCCCTTAAAATGATAAGAGTGACACGGCTTCCACCCTAGAGATACAGTCCCAGCCTCAAGGACCTTCTGGTCTGATGGAGGAGGTAAAACAT... | AAAAGAACCTTGCTCTAGGGAAACCTGCAGTCTGGTGAAAAAAGGACAACTCCTGCCCAGGGAGTCCGTCGTCTTGACGTGGGAGGCATACCCATCACCTAAGGATGCTCCGATTTTGAGAGAAAGGGAGATATCCTATCCATGCCTTGGGGGACTCCCAGTCCGATGGAAAAGGCACAACTCTAGGGAAGCCCTTGTTCTGTTAGCGACAGATGCCATTCTAGGAGAGCCCTTAAAATGATAAGAGTGACACGGCTTCCACCCTAGAGATACAGTCCCAGCCTCAAGGACCTTCTGGTCTGATGGAGGAGGTAAAACAT... |
Task1_train_45234 | A change on Chromosome 17 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TGGAGGGATACAAAGCCTCCAACTGTTGTCTCTGCCTCCTGCCTCACCTTCTTGAACCCAACTCCCACAGTAATTATTCGTCTAGTGGGTTCTGTTCCCAGTCCCACCTCTACCTGGATGAAGATGCTCTGCAGATTCTCTCTGCCTGCTATGGTGCTTCAGACTCTTCACAAACAACCCTGGCTTTCTCGTCTTCCTGCTCTCATCTACTCCCTCTTGCCCCCAAGACCTCCCTCCTGCCAGCAAGTTTTCTCTCACCTCTCCCTGAATGCATCATGCACTTTTACACCAACAAGCTCATTATCTGTCTGTACCTCCAC... | TGGAGGGATACAAAGCCTCCAACTGTTGTCTCTGCCTCCTGCCTCACCTTCTTGAACCCAACTCCCACAGTAATTATTCGTCTAGTGGGTTCTGTTCCCAGTCCCACCTCTACCTGGATGAAGATGCTCTGCAGATTCTCTCTGCCTGCTATGGTGCTTCAGACTCTTCACAAACAACCCTGGCTTTCTCGTCTTCCTGCTCTCATCTACTCCCTCTTGCCCCCAAGACCTCCCTCCTGCCAGCAAGTTTTCTCTCACCTCTCCCTGAATGCATCATGCACTTTTACACCAACAAGCTCATTATCTGTCTGTACCTCCAC... |
Task1_train_45235 | This mutation on Chromosome 17 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | ACGCGCGGAATCGGCCGGCCCGGAAGTGCCAGCTGCCTGCGTCGGCCGGAAGTGCCGCGCGGGAGGCGGAAGCGGCTGGTTCCCGCGTGGTTTGGCGGGTGCAGCGGCAGTCCGGCTGCCCTTCCCACGTAGACCGTCTGCTGGGGGCGCCGGCACCATTTGGAGTACGTGAGGTATACGGGTAGGGCGCGGCCAGGTCGGGCGTCTGTTAGGAAAAAGACTTTTTATTTTTATGTTTATTTTTTAAGAGACGGAGTCTCGCTCTGTCGCCCAGGTAGGAGTGCAGTGGCGCGATCTCGGCTCACTGCTGCCTTCCACCT... | ACGCGCGGAATCGGCCGGCCCGGAAGTGCCAGCTGCCTGCGTCGGCCGGAAGTGCCGCGCGGGAGGCGGAAGCGGCTGGTTCCCGCGTGGTTTGGCGGGTGCAGCGGCAGTCCGGCTGCCCTTCCCACGTAGACCGTCTGCTGGGGGCGCCGGCACCATTTGGAGTACGTGAGGTATACGGGTAGGGCGCGGCCAGGTCGGGCGTCTGTTAGGAAAAAGACTTTTTATTTTTATGTTTATTTTTTAAGAGACGGAGTCTCGCTCTGTCGCCCAGGTAGGAGTGCAGTGGCGCGATCTCGGCTCACTGCTGCCTTCCACCT... |
Task1_train_45236 | A change on Chromosome 17 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TAAAATGTAGCTGTTATGGAGTAAAGCTCTTGACTCTCTCTTAATGTTGATCCTTAAAGGAAACAGACTTCATAGAAAATAGCAGCTGCAAAGCCTGTGGCAGCACTGAAGATGGTAATACTTGTGTAGAAGTAATTGTTACCAATGAAAATACATCATGTACCTGTCCTAGCAGTGGCAATCTTTTGGGGTCCCCTAAAATAAAGAAAGGTAAGTAAATAATTTCTTTTTAAAATGAACTCTTAACTCTATTCTTTCTTACTGTTAAATGTAAGAGCTTTTAGAGATTCTGTGAGCTAGAATTTTAAAACTGCTTTATA... | TAAAATGTAGCTGTTATGGAGTAAAGCTCTTGACTCTCTCTTAATGTTGATCCTTAAAGGAAACAGACTTCATAGAAAATAGCAGCTGCAAAGCCTGTGGCAGCACTGAAGATGGTAATACTTGTGTAGAAGTAATTGTTACCAATGAAAATACATCATGTACCTGTCCTAGCAGTGGCAATCTTTTGGGGTCCCCTAAAATAAAGAAAGGTAAGTAAATAATTTCTTTTTAAAATGAACTCTTAACTCTATTCTTTCTTACTGTTAAATGTAAGAGCTTTTAGAGATTCTGTGAGCTAGAATTTTAAAACTGCTTTATA... |
Task1_train_45237 | Here is a genetic alteration on Chromosome 17. Based on the data, is it a benign variant or a cause of disease? | Benign | AATAAATACAACAGATTTTACCAAATTTAGTTAGCATATTCTCCTTGAACTCAAATTACACTGTATTTTCCATGCAATTCTAATAAAGAGGCAGCAATTAGTTTTCATAGCCACTGATAAAAGTATCCAAGCTTTTACAACATGTCCTTGCCTCTCAAGTCATAGTAAGTTCACTTAAATGTTTTCAAAGAGGCCGGGTGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGTGGATCACGAGGTCAGGAGTTCAAGACCAGCCTGGTCAAGATGGTGAAACCCCATCTCTACTAAAAATGTAAA... | AATAAATACAACAGATTTTACCAAATTTAGTTAGCATATTCTCCTTGAACTCAAATTACACTGTATTTTCCATGCAATTCTAATAAAGAGGCAGCAATTAGTTTTCATAGCCACTGATAAAAGTATCCAAGCTTTTACAACATGTCCTTGCCTCTCAAGTCATAGTAAGTTCACTTAAATGTTTTCAAAGAGGCCGGGTGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGTGGATCACGAGGTCAGGAGTTCAAGACCAGCCTGGTCAAGATGGTGAAACCCCATCTCTACTAAAAATGTAAA... |
Task1_train_45238 | A change on Chromosome 17 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | GGGAGCCCGAGGCGGGCAGAACATGAGGTCAGGAATTCGAGACCAGCCTGGCCAACATAGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCGGGTGTAGTGGTGTGCGCCTGTTGTCCCAGACAGTCTGCATAGGAGGATGTCCTGGAAATGGTCAGAAGACAGTTCATGAAAATGTCCTCAAGTAAAATAGAAATTTGGAACTGTAAGGGTGAGAATGTTCTGCAATACAAATGCTCATCAGAAGATGTGGGTCAACATGGAATGTAGAAAAAGGTAAATGGAGACTATTTGTTATTATTTAAGAAATTTGGA... | GGGAGCCCGAGGCGGGCAGAACATGAGGTCAGGAATTCGAGACCAGCCTGGCCAACATAGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCGGGTGTAGTGGTGTGCGCCTGTTGTCCCAGACAGTCTGCATAGGAGGATGTCCTGGAAATGGTCAGAAGACAGTTCATGAAAATGTCCTCAAGTAAAATAGAAATTTGGAACTGTAAGGGTGAGAATGTTCTGCAATACAAATGCTCATCAGAAGATGTGGGTCAACATGGAATGTAGAAAAAGGTAAATGGAGACTATTTGTTATTATTTAAGAAATTTGGA... |
Task1_train_45239 | A change on Chromosome 17 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | ACAATATTAATTATTTTAATTAATATTTAATATTAAAATAAAAATTAATGATTTAAAATTTGTATCAATTGTTATTAAGATTCAGTATTAAGCTTAGGAAGTCTTAATTTAAAATACATTGTATTCTATGGTAGATTGTTTTTAGTTATTTGCTGCCTTTCTTCTTCTTTTTTTTTTTTTTTTTTGAGATGGAATCTCACTCTGTCGCCCAGGCGGGAGTGCAGTGGCGCAATCTCAGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGCGATTCTCCTGCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGCACCAC... | ACAATATTAATTATTTTAATTAATATTTAATATTAAAATAAAAATTAATGATTTAAAATTTGTATCAATTGTTATTAAGATTCAGTATTAAGCTTAGGAAGTCTTAATTTAAAATACATTGTATTCTATGGTAGATTGTTTTTAGTTATTTGCTGCCTTTCTTCTTCTTTTTTTTTTTTTTTTTTGAGATGGAATCTCACTCTGTCGCCCAGGCGGGAGTGCAGTGGCGCAATCTCAGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGCGATTCTCCTGCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGCACCAC... |
Task1_train_45240 | A mutation has occurred on Chromosome 17. What is the medical relevance of this mutation? | Benign | GCCTGCCTCGGCCTCCCAAAGTGCAGGGATTACAGGTGTGAGCCACCGCACCCGGCCTAATTTTTTAATTTTTTTGTAGAGATAGGGTTTTGCCATATTGGGCAGGCTGGTCTTGAACTCCTGGACTCAAGGGATCTAACCCACTTCCGCCTCTCAAAGTGCTGGGATTACAAGTGTGAGCCACCCCACACGACCCCACATACTCTTCAACACATACATACAGCACTAATTTCATGTCACTATTAATGTGTCGTGCTATAGGTTCAATACTGTGGCTGGAACTTGTAGGGAAATACTTACCACATAAGAATGTACGATAT... | GCCTGCCTCGGCCTCCCAAAGTGCAGGGATTACAGGTGTGAGCCACCGCACCCGGCCTAATTTTTTAATTTTTTTGTAGAGATAGGGTTTTGCCATATTGGGCAGGCTGGTCTTGAACTCCTGGACTCAAGGGATCTAACCCACTTCCGCCTCTCAAAGTGCTGGGATTACAAGTGTGAGCCACCCCACACGACCCCACATACTCTTCAACACATACATACAGCACTAATTTCATGTCACTATTAATGTGTCGTGCTATAGGTTCAATACTGTGGCTGGAACTTGTAGGGAAATACTTACCACATAAGAATGTACGATAT... |
Task1_train_45241 | With a mutation on Chromosome 17, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TTTAGCTTTTCCCCCAATTTATCTTCCGCTTCAATTAAATGGCTCTTCAGCTTTCTATGGTGGCCTTTATAGCCTTCTGTGGTCCACCATCCCTACGTTGCCAACACTTTGTATGGTTTAGTTTCTTCTCAAAAAATGCTCCATCGTAGACTTCAGAGAATTGGGTCCCCCTGTGAGAGAAGGTAGGCTGGGCACAACTGACTTTTTTCATCCCTAACAGTGGCTTTGTGGGTGAGTGTCCAGACTCGGGTGGTTTGTGTTGTGAGTACTGTAGGTGGATGGGAGGCGTCCTTAGAAGTAGAGTGTCCAGTCTTTGTTTC... | TTTAGCTTTTCCCCCAATTTATCTTCCGCTTCAATTAAATGGCTCTTCAGCTTTCTATGGTGGCCTTTATAGCCTTCTGTGGTCCACCATCCCTACGTTGCCAACACTTTGTATGGTTTAGTTTCTTCTCAAAAAATGCTCCATCGTAGACTTCAGAGAATTGGGTCCCCCTGTGAGAGAAGGTAGGCTGGGCACAACTGACTTTTTTCATCCCTAACAGTGGCTTTGTGGGTGAGTGTCCAGACTCGGGTGGTTTGTGTTGTGAGTACTGTAGGTGGATGGGAGGCGTCCTTAGAAGTAGAGTGTCCAGTCTTTGTTTC... |
Task1_train_45242 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | GTCCAATCCCTTCCCAGTAGTTCCTTCACTTACCTCCCAGGGACAGATCTTGGCTTTTTCACTGGTAGCAGCTTCCTGTGCTTCCCAGGGACACACTTCACCTGGCCTGCAGCCCATATGATCCAGTTCCTGGAACCCAGCTTTTGGTCCATCAGCATCTAGAGTACCTGGATGCTGAGAACAGGCCCCTGGACCCACACTCCCCCAGGGACAAGCCACCTCCCACTCTGGGGTTGGCTTCTGTGGCTTCTCTGGAGCAGTAACAGCTCTCTCCCTGGGTCCAAGATCTGCAGAAACCTTGCCTGTATCATTTGGAGATT... | GTCCAATCCCTTCCCAGTAGTTCCTTCACTTACCTCCCAGGGACAGATCTTGGCTTTTTCACTGGTAGCAGCTTCCTGTGCTTCCCAGGGACACACTTCACCTGGCCTGCAGCCCATATGATCCAGTTCCTGGAACCCAGCTTTTGGTCCATCAGCATCTAGAGTACCTGGATGCTGAGAACAGGCCCCTGGACCCACACTCCCCCAGGGACAAGCCACCTCCCACTCTGGGGTTGGCTTCTGTGGCTTCTCTGGAGCAGTAACAGCTCTCTCCCTGGGTCCAAGATCTGCAGAAACCTTGCCTGTATCATTTGGAGATT... |
Task1_train_45243 | A variant on Chromosome 17 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | CTTGTAGGGTGAGTAGGAGCTCATCCAGCAAATAGGGCAGGGGGACATTAAGGGCTGGCAGCAATGTAACAGTGTAGGTCACATCAAAGGAAGGGTTGGTAGGGCTGTATTTCCACAGTGAGGGCTGTGTTGGGGTTGGGGTCAGGGCAGAGCAGGGCAGTAGGCTGGGAAAGTTGGGGCTGGGTTATGAAGAGCCCCATGTGCTGAACTGGGGAACTTGTGCTTTATCCTGGTGGGTGCTGGGGCATGCAAGCTTCTGAGCAAAGCTGGGTGAGGATCAGATTCCTGCTTCAGAATGGTGGCTCTGGAGGAGAGACCCG... | CTTGTAGGGTGAGTAGGAGCTCATCCAGCAAATAGGGCAGGGGGACATTAAGGGCTGGCAGCAATGTAACAGTGTAGGTCACATCAAAGGAAGGGTTGGTAGGGCTGTATTTCCACAGTGAGGGCTGTGTTGGGGTTGGGGTCAGGGCAGAGCAGGGCAGTAGGCTGGGAAAGTTGGGGCTGGGTTATGAAGAGCCCCATGTGCTGAACTGGGGAACTTGTGCTTTATCCTGGTGGGTGCTGGGGCATGCAAGCTTCTGAGCAAAGCTGGGTGAGGATCAGATTCCTGCTTCAGAATGGTGGCTCTGGAGGAGAGACCCG... |
Task1_train_45244 | This genomic variant is located on Chromosome 17. Can you determine its pathogenicity and name any linked disease? | Benign | CCCTAGGGATGGGCAAGCTTGGCTCCCATGAACCTCCCCAAGTACCAGGCCTGCCCGCGGGGCACTGGGGATCCAGAGGCGCAAGCAGAGAGATGACAGAGACAGAGAATCAGAGACAGGAAGGGGAGGGGAGCATGGGGATGGAAGGTGGGGAGAGAACTTTATTTGTTGGTTTACAGATACAGAGCAGAAGGGGGAGGCCCTGGTTCTTGCCAAGGCTGGGGATTGGCCGGCCCCTGGGTAGGCCGGCTTCCCAGCCTCCCCCGGACTCTGCCTGCAAACCCTGCTCTGGCACCAGGCTCCCAGGAGAGTGGTAAGAG... | CCCTAGGGATGGGCAAGCTTGGCTCCCATGAACCTCCCCAAGTACCAGGCCTGCCCGCGGGGCACTGGGGATCCAGAGGCGCAAGCAGAGAGATGACAGAGACAGAGAATCAGAGACAGGAAGGGGAGGGGAGCATGGGGATGGAAGGTGGGGAGAGAACTTTATTTGTTGGTTTACAGATACAGAGCAGAAGGGGGAGGCCCTGGTTCTTGCCAAGGCTGGGGATTGGCCGGCCCCTGGGTAGGCCGGCTTCCCAGCCTCCCCCGGACTCTGCCTGCAAACCCTGCTCTGGCACCAGGCTCCCAGGAGAGTGGTAAGAG... |
Task1_train_45245 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | GTACCAGGCCTGCCCGCGGGGCACTGGGGATCCAGAGGCGCAAGCAGAGAGATGACAGAGACAGAGAATCAGAGACAGGAAGGGGAGGGGAGCATGGGGATGGAAGGTGGGGAGAGAACTTTATTTGTTGGTTTACAGATACAGAGCAGAAGGGGGAGGCCCTGGTTCTTGCCAAGGCTGGGGATTGGCCGGCCCCTGGGTAGGCCGGCTTCCCAGCCTCCCCCGGACTCTGCCTGCAAACCCTGCTCTGGCACCAGGCTCCCAGGAGAGTGGTAAGAGCTGAGAGAAGGCCGGTGGGAGGAGGGGGCTGGCCTGGCATT... | GTACCAGGCCTGCCCGCGGGGCACTGGGGATCCAGAGGCGCAAGCAGAGAGATGACAGAGACAGAGAATCAGAGACAGGAAGGGGAGGGGAGCATGGGGATGGAAGGTGGGGAGAGAACTTTATTTGTTGGTTTACAGATACAGAGCAGAAGGGGGAGGCCCTGGTTCTTGCCAAGGCTGGGGATTGGCCGGCCCCTGGGTAGGCCGGCTTCCCAGCCTCCCCCGGACTCTGCCTGCAAACCCTGCTCTGGCACCAGGCTCCCAGGAGAGTGGTAAGAGCTGAGAGAAGGCCGGTGGGAGGAGGGGGCTGGCCTGGCATT... |
Task1_train_45246 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | CTTGGGGGGCACAACCTGTCCCCCACCCCCCACAAATCCTAGAGTCCAGAGCCTCAGCTACCAGGAGACTCACCCTCAGCAGCTTGTGCCCAAGCAGGGGTCCCTAGGTCAGGAAACCAGGCTTAAAGCTAGACCTAAGTCTGCTGGGCCTCTGAGGCAGTCTGTGTCCCTCTCTGGGCCTCAAGGACATAAATGAAGAAAGAAAACAGATTTCCTTGCCAGGGCTTGGAGGAGATAAATGCTTGAGATTCCTCGAAAGAGCAGCTTTTATGGCAAGCCCTGGATCCTTCCCCTGAACTCCCTGCCTGCCCAGCACCCAC... | CTTGGGGGGCACAACCTGTCCCCCACCCCCCACAAATCCTAGAGTCCAGAGCCTCAGCTACCAGGAGACTCACCCTCAGCAGCTTGTGCCCAAGCAGGGGTCCCTAGGTCAGGAAACCAGGCTTAAAGCTAGACCTAAGTCTGCTGGGCCTCTGAGGCAGTCTGTGTCCCTCTCTGGGCCTCAAGGACATAAATGAAGAAAGAAAACAGATTTCCTTGCCAGGGCTTGGAGGAGATAAATGCTTGAGATTCCTCGAAAGAGCAGCTTTTATGGCAAGCCCTGGATCCTTCCCCTGAACTCCCTGCCTGCCCAGCACCCAC... |
Task1_train_45247 | A variant found on Chromosome 17 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | AAACCCCAGGGGACTCTTGAAGTTAGGCCAAGAGTCCTTTCATTTACCACCTCTGCAAAGTGCAGCTTGTTTTGTTTCCACTCTTTAAGGGGGCTGAGTTTGGGTGTCCAAAGAATGGACTTGGGCCTGCCTTCCACCTCCACCCCCTCTCATCCATAAATCGGTGGAGGCCCTCGAAAGGCGACTTGTTTGGTCTGATTTTATTGATTTCTTCCACCTTCTATTACTTTCCCTGGGACAGTGTCTAGCCCCTTCCCCAGGCAAAGTAAGCACTTTCCAGGAGAGGAGGTCCCTCAGCCCTACCCGTCCTAAGGGAAGTA... | AAACCCCAGGGGACTCTTGAAGTTAGGCCAAGAGTCCTTTCATTTACCACCTCTGCAAAGTGCAGCTTGTTTTGTTTCCACTCTTTAAGGGGGCTGAGTTTGGGTGTCCAAAGAATGGACTTGGGCCTGCCTTCCACCTCCACCCCCTCTCATCCATAAATCGGTGGAGGCCCTCGAAAGGCGACTTGTTTGGTCTGATTTTATTGATTTCTTCCACCTTCTATTACTTTCCCTGGGACAGTGTCTAGCCCCTTCCCCAGGCAAAGTAAGCACTTTCCAGGAGAGGAGGTCCCTCAGCCCTACCCGTCCTAAGGGAAGTA... |
Task1_train_45248 | A mutation on Chromosome 17 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | AGGCCGGACGGTGCTTCCAGGGCTTGAGCTAACCCTGAGCCCCTCATCTTCCCTGGCCACAGGCCCAGTGGTTCCCTAGAACCCCAGCCAGGTCCGTGGTGGCCCTGAAGACCCCCATCAAGGTGGAGCTGGTGGCAGGGAAAACCTACAGGTGGTGTGTGTGTGGCCGCAGCAAGAAGCAGGTGAGACCCCTGTCTGCCTTCCTACTGATACCTCTGGCTAGGAACAGCCTGGTGTCTCCAGTGAGTTCCCACCCAGGATGATCTTATTCTTCCCACACATACCTGAGGGACACCAAGGGGGCTTGGGAACAAAAGGCC... | AGGCCGGACGGTGCTTCCAGGGCTTGAGCTAACCCTGAGCCCCTCATCTTCCCTGGCCACAGGCCCAGTGGTTCCCTAGAACCCCAGCCAGGTCCGTGGTGGCCCTGAAGACCCCCATCAAGGTGGAGCTGGTGGCAGGGAAAACCTACAGGTGGTGTGTGTGTGGCCGCAGCAAGAAGCAGGTGAGACCCCTGTCTGCCTTCCTACTGATACCTCTGGCTAGGAACAGCCTGGTGTCTCCAGTGAGTTCCCACCCAGGATGATCTTATTCTTCCCACACATACCTGAGGGACACCAAGGGGGCTTGGGAACAAAAGGCC... |
Task1_train_45249 | Chromosome 17 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | CCTTTTTTTCTGATGCTTCTAATATTAAATGCGTCTATTTTCCCACTCTCCATTGTCTTGAGGTCTTCCCCTACCCACCCTGCCTAGTTCTGTCACGTCCCTTCTTTCCCTGTATCACAACAATGTTCTCCCTTTCTCACCTTTGTTTCTCTTCATACTTGTTTCTCTCTCTGTGTCTCTCTCATTCTCTTCCCTTCCAAATGTAGTATTTGGAGACTGTAATATCGATTGAGGCAGACAATAGAAAACTGTCGAACCTCCACTGTAAATTCATTCTTAATCCTATGAAAAAATGCATCCTGAAACGTGTTGCATGCACA... | CCTTTTTTTCTGATGCTTCTAATATTAAATGCGTCTATTTTCCCACTCTCCATTGTCTTGAGGTCTTCCCCTACCCACCCTGCCTAGTTCTGTCACGTCCCTTCTTTCCCTGTATCACAACAATGTTCTCCCTTTCTCACCTTTGTTTCTCTTCATACTTGTTTCTCTCTCTGTGTCTCTCTCATTCTCTTCCCTTCCAAATGTAGTATTTGGAGACTGTAATATCGATTGAGGCAGACAATAGAAAACTGTCGAACCTCCACTGTAAATTCATTCTTAATCCTATGAAAAAATGCATCCTGAAACGTGTTGCATGCACA... |
Task1_train_45250 | Consider a variant on Chromosome 17. Determine its clinical classification and disease relevance. | Benign | TAAATACTCAAGTTCTTCCTTTTCCCCTCCCCAGACTCTGGTTCCTTCTGTCGTAAAATTACGAGTCGATGCCAGCATGGTGGCTCATGCCTATAGTCCCAGCACTTTGGGAGGCCGAGATGGGCAGAACACTTGAGCTCAGGAGTTTAAGACCAGCCTGGGCAACATGGTGAAACCCTGTCTCTGTAGTCTCAGCTACTAGAGTGGCTGAAGTGGGAGGATCGCTTGAACACGGAAAGCAGAGGTTGCAGTAAGCCAAAATTATGCCACTGCACTCCAGCCAGGGTGACAGAACAAGACCCTGTCTCAAAAAAAAAAAA... | TAAATACTCAAGTTCTTCCTTTTCCCCTCCCCAGACTCTGGTTCCTTCTGTCGTAAAATTACGAGTCGATGCCAGCATGGTGGCTCATGCCTATAGTCCCAGCACTTTGGGAGGCCGAGATGGGCAGAACACTTGAGCTCAGGAGTTTAAGACCAGCCTGGGCAACATGGTGAAACCCTGTCTCTGTAGTCTCAGCTACTAGAGTGGCTGAAGTGGGAGGATCGCTTGAACACGGAAAGCAGAGGTTGCAGTAAGCCAAAATTATGCCACTGCACTCCAGCCAGGGTGACAGAACAAGACCCTGTCTCAAAAAAAAAAAA... |
Task1_train_45251 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | AGTCAGAGACAGGTTATTGCCATGTCATGGAGGCTCTTACAAATGTACTAATAATATAAACAAAGCAATTCTCCTACACATAGGTCAGCAGGCAAAGTGTTCTAATCCTGTGCAAGGAAAGCATCCTTGTAAACTTTAGAATCTAAAGGATTATGCAGGAATAGGAATAATTGTTTCACCTTTCCTTTACTCACAGAAGAGGGCTTTTTACAGAACCTAGGAGGGTGTTTCTGAGAATTTACAACATGGGAGTAATTGAGCTAATTAAATGAAGAAGCTTTCAAATAATAATAATAATAAATGTTTATTTATAAAATTGG... | AGTCAGAGACAGGTTATTGCCATGTCATGGAGGCTCTTACAAATGTACTAATAATATAAACAAAGCAATTCTCCTACACATAGGTCAGCAGGCAAAGTGTTCTAATCCTGTGCAAGGAAAGCATCCTTGTAAACTTTAGAATCTAAAGGATTATGCAGGAATAGGAATAATTGTTTCACCTTTCCTTTACTCACAGAAGAGGGCTTTTTACAGAACCTAGGAGGGTGTTTCTGAGAATTTACAACATGGGAGTAATTGAGCTAATTAAATGAAGAAGCTTTCAAATAATAATAATAATAAATGTTTATTTATAAAATTGG... |
Task1_train_45252 | A mutation is present on Chromosome 17. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GTAGTTGGCAGGTGCCTCTCCAACCTGGTGTCTTTGGGCATCCTTGCCCTGGGCGACACAGTGAGACCCTGTCTCAAAAAAAGTCCCTCCCATGCCAGCTGCCTGTGTCCCAACCACTCAGGTGCTTTGCCTCTCAACAGAATCCACCTGCAGTTCCCTGCTAGGTATGTCTCAAGGAGCCCTCTAGCCACCCGACTTGTCTTTAATGCCTATAAAATCCAGTTCAGAGGAGGAAAAATATTTATCAGGCAAGTCCTGCCTTTGGAGGTATGTACAGGCACTGACATCAGAACAGGGCAGTGAGTAAACCCGGCACCGAA... | GTAGTTGGCAGGTGCCTCTCCAACCTGGTGTCTTTGGGCATCCTTGCCCTGGGCGACACAGTGAGACCCTGTCTCAAAAAAAGTCCCTCCCATGCCAGCTGCCTGTGTCCCAACCACTCAGGTGCTTTGCCTCTCAACAGAATCCACCTGCAGTTCCCTGCTAGGTATGTCTCAAGGAGCCCTCTAGCCACCCGACTTGTCTTTAATGCCTATAAAATCCAGTTCAGAGGAGGAAAAATATTTATCAGGCAAGTCCTGCCTTTGGAGGTATGTACAGGCACTGACATCAGAACAGGGCAGTGAGTAAACCCGGCACCGAA... |
Task1_train_45253 | Here is a variant on Chromosome 17. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GTTTTCCAGGCCTGATGTAAGGCCCTTTCTACGTGGCCCAGCTCCTTAAAATCCTCCAGGTGATTACTCAATATCTACCTGCTTAGTGTCCCTTGTCAGATAACTTACCTAAAATTGCAACATTCCCTCCACACACTTCCACTCTCCCTTTTCTTTTCTTTGTTTTTGCTTTTGGAAATGGGGGTCTGGATATGTTGCCCAGGCTGGACTCCAACTCCTGGCCCCAAGCCATCCTCCTGCCTCAGACTCTCCAGTAGCTAGAACTACAGGCATGAACCACCATGCTGGCCCAATCTCTGTTTCTTACTCTTTATTCACCT... | GTTTTCCAGGCCTGATGTAAGGCCCTTTCTACGTGGCCCAGCTCCTTAAAATCCTCCAGGTGATTACTCAATATCTACCTGCTTAGTGTCCCTTGTCAGATAACTTACCTAAAATTGCAACATTCCCTCCACACACTTCCACTCTCCCTTTTCTTTTCTTTGTTTTTGCTTTTGGAAATGGGGGTCTGGATATGTTGCCCAGGCTGGACTCCAACTCCTGGCCCCAAGCCATCCTCCTGCCTCAGACTCTCCAGTAGCTAGAACTACAGGCATGAACCACCATGCTGGCCCAATCTCTGTTTCTTACTCTTTATTCACCT... |
Task1_train_45254 | Given a variant located on Chromosome 17, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AGCATCCTGTAGAGCCTGTGGACAGAGGAGCCCAGCCCCAGTCAGCCTGCTAGTGCCCAGCCTTCCTTCCTACTGCCTCACAGGCGCTCTCTGGCTCCCTCTCCAGCTGTCCCAGGAAGAGAGGCCCATGCCTGGATGGGGCAGAGATGGGGGCCCTGCCACAATGGTAGCAACCGTATCAAATAACATCAGCAGCTCAAGGAAAGCCTCTTTATGACAATCCCATAGGTGGGAATTGATGATCCTCCTCATTTTATACTTGGGGAAACTGAGGATTAGAGAGGTGAAGTCACTTGTCCAAAGTCCTACAGTGAATGAAA... | AGCATCCTGTAGAGCCTGTGGACAGAGGAGCCCAGCCCCAGTCAGCCTGCTAGTGCCCAGCCTTCCTTCCTACTGCCTCACAGGCGCTCTCTGGCTCCCTCTCCAGCTGTCCCAGGAAGAGAGGCCCATGCCTGGATGGGGCAGAGATGGGGGCCCTGCCACAATGGTAGCAACCGTATCAAATAACATCAGCAGCTCAAGGAAAGCCTCTTTATGACAATCCCATAGGTGGGAATTGATGATCCTCCTCATTTTATACTTGGGGAAACTGAGGATTAGAGAGGTGAAGTCACTTGTCCAAAGTCCTACAGTGAATGAAA... |
Task1_train_45255 | This alteration on Chromosome 17 may affect genome function. Does it lead to a disease or is it benign? | Benign | CCCAGTCAGCCTGCTAGTGCCCAGCCTTCCTTCCTACTGCCTCACAGGCGCTCTCTGGCTCCCTCTCCAGCTGTCCCAGGAAGAGAGGCCCATGCCTGGATGGGGCAGAGATGGGGGCCCTGCCACAATGGTAGCAACCGTATCAAATAACATCAGCAGCTCAAGGAAAGCCTCTTTATGACAATCCCATAGGTGGGAATTGATGATCCTCCTCATTTTATACTTGGGGAAACTGAGGATTAGAGAGGTGAAGTCACTTGTCCAAAGTCCTACAGTGAATGAAAGATGGAGTTAGAACTTGAACCAGCAACTCTGGCTTC... | CCCAGTCAGCCTGCTAGTGCCCAGCCTTCCTTCCTACTGCCTCACAGGCGCTCTCTGGCTCCCTCTCCAGCTGTCCCAGGAAGAGAGGCCCATGCCTGGATGGGGCAGAGATGGGGGCCCTGCCACAATGGTAGCAACCGTATCAAATAACATCAGCAGCTCAAGGAAAGCCTCTTTATGACAATCCCATAGGTGGGAATTGATGATCCTCCTCATTTTATACTTGGGGAAACTGAGGATTAGAGAGGTGAAGTCACTTGTCCAAAGTCCTACAGTGAATGAAAGATGGAGTTAGAACTTGAACCAGCAACTCTGGCTTC... |
Task1_train_45256 | Here is a variant on Chromosome 17. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GCCTCACAGGCGCTCTCTGGCTCCCTCTCCAGCTGTCCCAGGAAGAGAGGCCCATGCCTGGATGGGGCAGAGATGGGGGCCCTGCCACAATGGTAGCAACCGTATCAAATAACATCAGCAGCTCAAGGAAAGCCTCTTTATGACAATCCCATAGGTGGGAATTGATGATCCTCCTCATTTTATACTTGGGGAAACTGAGGATTAGAGAGGTGAAGTCACTTGTCCAAAGTCCTACAGTGAATGAAAGATGGAGTTAGAACTTGAACCAGCAACTCTGGCTTCTATAGTCAATTGCACTGAGGGTACTGATGCCCTTCATC... | GCCTCACAGGCGCTCTCTGGCTCCCTCTCCAGCTGTCCCAGGAAGAGAGGCCCATGCCTGGATGGGGCAGAGATGGGGGCCCTGCCACAATGGTAGCAACCGTATCAAATAACATCAGCAGCTCAAGGAAAGCCTCTTTATGACAATCCCATAGGTGGGAATTGATGATCCTCCTCATTTTATACTTGGGGAAACTGAGGATTAGAGAGGTGAAGTCACTTGTCCAAAGTCCTACAGTGAATGAAAGATGGAGTTAGAACTTGAACCAGCAACTCTGGCTTCTATAGTCAATTGCACTGAGGGTACTGATGCCCTTCATC... |
Task1_train_45257 | Given this variant on Chromosome 17, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CTCTCTCTACAGCCCAGGACTGGGGGAAATCATGCCAGCACAGCCCCTCCCCACATCTTTCTCACCTTGGCCTTCTCGAGCTGCGCTAATGCCTGGCGCTCTGCTTCCTTCCTTAAGGCTTCCCGGTCCTCCTCCAGAGATACATCAGAGTCTGATGGACGGCTGGTGTAGGACTCCGCTGAGCCCTGAAAATAGAGAGAGCCAGATCAGGGCCATTGCTGCCCCTCCCAGCTCCTGGGCCTGGGAAGGCATGGAGGTGCCACCCATCATGGATGCCTCGAGCCCCAGCCAGCCCAGCATGACACCACAAGGGCTAAGAC... | CTCTCTCTACAGCCCAGGACTGGGGGAAATCATGCCAGCACAGCCCCTCCCCACATCTTTCTCACCTTGGCCTTCTCGAGCTGCGCTAATGCCTGGCGCTCTGCTTCCTTCCTTAAGGCTTCCCGGTCCTCCTCCAGAGATACATCAGAGTCTGATGGACGGCTGGTGTAGGACTCCGCTGAGCCCTGAAAATAGAGAGAGCCAGATCAGGGCCATTGCTGCCCCTCCCAGCTCCTGGGCCTGGGAAGGCATGGAGGTGCCACCCATCATGGATGCCTCGAGCCCCAGCCAGCCCAGCATGACACCACAAGGGCTAAGAC... |
Task1_train_45258 | Chromosome 17 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CAAGGACTCAGTAGGGTCGTGCTGAGCAGGGGGTTTGGAGCCAGAGAGTGGCAAAGCAGGGGCTGAGACTTGGCTCTCCCGAGTCCTGATCGGTCAGCACCGGTGGGTGCCCAGGCTGGAAAGAGGAAGGAGGACAGAGCTCTGAGGCCTAGTGACTGAGGGTGGAAGGGGCTGCAGAGCCCAGGGCAGAGTCTGAGGAGCAAGAGGAGTGCTGGGTGGTGTGGGTTGGGTGGGATGGGGTGGGTGGGTGGCAGGCCTGGGGGCCTCACCGGCAGCCAGAGGAGAGGTGGCATCAGATTTCATGGAGCTGGGGTGGGCTT... | CAAGGACTCAGTAGGGTCGTGCTGAGCAGGGGGTTTGGAGCCAGAGAGTGGCAAAGCAGGGGCTGAGACTTGGCTCTCCCGAGTCCTGATCGGTCAGCACCGGTGGGTGCCCAGGCTGGAAAGAGGAAGGAGGACAGAGCTCTGAGGCCTAGTGACTGAGGGTGGAAGGGGCTGCAGAGCCCAGGGCAGAGTCTGAGGAGCAAGAGGAGTGCTGGGTGGTGTGGGTTGGGTGGGATGGGGTGGGTGGGTGGCAGGCCTGGGGGCCTCACCGGCAGCCAGAGGAGAGGTGGCATCAGATTTCATGGAGCTGGGGTGGGCTT... |
Task1_train_45259 | A variant found on Chromosome 17 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | CCTTGGGTCATTGTCCCCTGAACTAACCCTCCCTCCCGCAGGGACTTCGTGAATGTCCGGCGCATTGAGCGGCGCAGGGACCGATACTTGTCATCAGGGATCGCCACCTCACACAGTGCCAAGCCCCCGACGCACAAATATGTCCGGTGAGCCTCACTTTGCCTGGGGTCACCCCTGCCAGCCCCTCCCCTGGGAGCATTGAGCAGTGCAGGGTACAGCATGTACAGCTGGGCACTTCCCCTGCTGAGGCTGCGTTCCTGTTCCCTGTCCCGCTGGGCTCTGCTCCTCCTGGCTACTAATCCTGCTAATCTTGCTGCTCT... | CCTTGGGTCATTGTCCCCTGAACTAACCCTCCCTCCCGCAGGGACTTCGTGAATGTCCGGCGCATTGAGCGGCGCAGGGACCGATACTTGTCATCAGGGATCGCCACCTCACACAGTGCCAAGCCCCCGACGCACAAATATGTCCGGTGAGCCTCACTTTGCCTGGGGTCACCCCTGCCAGCCCCTCCCCTGGGAGCATTGAGCAGTGCAGGGTACAGCATGTACAGCTGGGCACTTCCCCTGCTGAGGCTGCGTTCCTGTTCCCTGTCCCGCTGGGCTCTGCTCCTCCTGGCTACTAATCCTGCTAATCTTGCTGCTCT... |
Task1_train_45260 | A variant on Chromosome 17 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | AGTGGCACCTAATAAAGAAATAATACCCTGCCGCTGCGGTCAGTGCTGTGTGTGGCTCTCCTGGGAAGCAGCAAGGGCCCAGAGATCTGAGTGTCCGGGTAGGGGAGACATTCACCCTAGGCTTTTTTTCCAGAAGCTTCCTTGAGGCTAGCATTCTGTACCACTCATTCTTCCCAAACTAAGGAAGGCCAAGGTCAGGGGAGCTCACCGGGCACCTGCAGTGCACCAGGCACTTGTGATATGCCATTGTGTCCATCGCATCATTCATTCCTGCATTCAGCAGCAGGTCCTGCTAGTCTGTTTCCAGGTGAAGCTCAGAG... | AGTGGCACCTAATAAAGAAATAATACCCTGCCGCTGCGGTCAGTGCTGTGTGTGGCTCTCCTGGGAAGCAGCAAGGGCCCAGAGATCTGAGTGTCCGGGTAGGGGAGACATTCACCCTAGGCTTTTTTTCCAGAAGCTTCCTTGAGGCTAGCATTCTGTACCACTCATTCTTCCCAAACTAAGGAAGGCCAAGGTCAGGGGAGCTCACCGGGCACCTGCAGTGCACCAGGCACTTGTGATATGCCATTGTGTCCATCGCATCATTCATTCCTGCATTCAGCAGCAGGTCCTGCTAGTCTGTTTCCAGGTGAAGCTCAGAG... |
Task1_train_45261 | A variant on Chromosome 17 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TTTAGTAGAGACAGGGTTTCTCCATGTTGGTCAGGCTGGTACCAAACTCCCGACCTCAGGTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGCAATTACAGGCATGAGCCACCGCACCCAGCCGTGCTAGGGTCTTTTTCTGTTCAATTCCTTTCTCTCTCTTGCTCTCTTTCTTTCTTTCAATGGAGTCTTACTCTGTCACCCAGGCTGGAGTGCAGTGGCAAGATCTCAGCTCACTGCAACCTCTGCCCTCTGAGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGTGCCTGCCACCACAC... | TTTAGTAGAGACAGGGTTTCTCCATGTTGGTCAGGCTGGTACCAAACTCCCGACCTCAGGTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGCAATTACAGGCATGAGCCACCGCACCCAGCCGTGCTAGGGTCTTTTTCTGTTCAATTCCTTTCTCTCTCTTGCTCTCTTTCTTTCTTTCAATGGAGTCTTACTCTGTCACCCAGGCTGGAGTGCAGTGGCAAGATCTCAGCTCACTGCAACCTCTGCCCTCTGAGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGTGCCTGCCACCACAC... |
Task1_train_45262 | With a mutation on Chromosome 17, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | ATGGAGTCTTGCTCTGTTGCCCAGGCTGGAGTGCAATGACACGATCTTGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCAGTTCAAGCAATCCTCCTGTCTCAGCCCCCCAGTAGCTGGGATTACAGGCATGCGCTACCACGTCCGGCTAATTTTTGTATTTTTAGTAGAGATGAGGTTTTGCCATGTTGGCCAGGCTGGTCTTGAACTGCTGACCTCAGGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCATCGTGCCTGGCGGAGCCGAGTCTTAAAAGATGACCCTGTGGAGAA... | ATGGAGTCTTGCTCTGTTGCCCAGGCTGGAGTGCAATGACACGATCTTGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCAGTTCAAGCAATCCTCCTGTCTCAGCCCCCCAGTAGCTGGGATTACAGGCATGCGCTACCACGTCCGGCTAATTTTTGTATTTTTAGTAGAGATGAGGTTTTGCCATGTTGGCCAGGCTGGTCTTGAACTGCTGACCTCAGGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCATCGTGCCTGGCGGAGCCGAGTCTTAAAAGATGACCCTGTGGAGAA... |
Task1_train_45263 | A variant on Chromosome 17 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GGGGCCAAACCTTACGATGGGATCCCAGCCCGGGAGATCCCTGACCTGCTGGAAAAGGGGGAGCGGCTGCCCCAGCCCCCCATCTGCACCATTGATGTCTACATGATCATGGTCAAATGTGCGTGGCTGAGCTGTGCTGGCTGCCTGGAGGAGGGTGGGAGGTCCTGGGTGGAGGAGCCCACAAGGGGCATGAAAGGGGACCAGGATGTATGTAGACCCAGGAGCCCTAGTATGTTAGGAGCCTCAAAACCTTCTTGTATCCCTTTTACAGTCAAAGTCCAAAGCCACTCTTGAGGAACACTCTTGTACAAAATTAAGCT... | GGGGCCAAACCTTACGATGGGATCCCAGCCCGGGAGATCCCTGACCTGCTGGAAAAGGGGGAGCGGCTGCCCCAGCCCCCCATCTGCACCATTGATGTCTACATGATCATGGTCAAATGTGCGTGGCTGAGCTGTGCTGGCTGCCTGGAGGAGGGTGGGAGGTCCTGGGTGGAGGAGCCCACAAGGGGCATGAAAGGGGACCAGGATGTATGTAGACCCAGGAGCCCTAGTATGTTAGGAGCCTCAAAACCTTCTTGTATCCCTTTTACAGTCAAAGTCCAAAGCCACTCTTGAGGAACACTCTTGTACAAAATTAAGCT... |
Task1_train_45264 | This alteration occurs on Chromosome 17. Is it associated with a disease or is it a benign variant? | Benign | GTGCCCAGGCCTTTTCTGAACTTTTAATTGCTTCCACCAACCCTCCAAAAAATTATGATTTGAGTGAGTTCTGAATCTGTACATTAAAATGAACTTTAAATATATCATGTGTATTTTTATAAACAAAAGTGTAATATGGAAAAATATCATGACTCGTGACTAACAGTGTAGAGTTTTAAAAAACTTACTATGAGAAGCAAAAAGGACTTCAGACGAGCGTTCTAAATGTTATATATTGATTTTTAAAATAGTGAAATCCAACAAGAACTAATTCGTGTCTTCAGCACAAAATGGTAGGAGTATATTTCTTAATTTAATTT... | GTGCCCAGGCCTTTTCTGAACTTTTAATTGCTTCCACCAACCCTCCAAAAAATTATGATTTGAGTGAGTTCTGAATCTGTACATTAAAATGAACTTTAAATATATCATGTGTATTTTTATAAACAAAAGTGTAATATGGAAAAATATCATGACTCGTGACTAACAGTGTAGAGTTTTAAAAAACTTACTATGAGAAGCAAAAAGGACTTCAGACGAGCGTTCTAAATGTTATATATTGATTTTTAAAATAGTGAAATCCAACAAGAACTAATTCGTGTCTTCAGCACAAAATGGTAGGAGTATATTTCTTAATTTAATTT... |
Task1_train_45265 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | ATGTTCTGATATTTCACTTACCTCTCTGGGTCTCTAGAAAGAAAGGGTAGGTCACAGAGTAACTTCACCTGCTAATTTATATTTGGGAAATGTTTGAATGTTTTATAACAAGCATACATTTCTTTAACTTTTAATTACAGTTTCTTTAAAAATATCAAATAGAACTAAAAAGCTGGCCAGGCGCGGTGGCTCACCGCTGTAATCCCAGTACTTTGGGAGGCCGAGGGGGGTGGATCACTGGAGCTCAGGAGTTCGAGACCAGCCTGGCCAACAAGGGTTAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGCAT... | ATGTTCTGATATTTCACTTACCTCTCTGGGTCTCTAGAAAGAAAGGGTAGGTCACAGAGTAACTTCACCTGCTAATTTATATTTGGGAAATGTTTGAATGTTTTATAACAAGCATACATTTCTTTAACTTTTAATTACAGTTTCTTTAAAAATATCAAATAGAACTAAAAAGCTGGCCAGGCGCGGTGGCTCACCGCTGTAATCCCAGTACTTTGGGAGGCCGAGGGGGGTGGATCACTGGAGCTCAGGAGTTCGAGACCAGCCTGGCCAACAAGGGTTAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGCAT... |
Task1_train_45266 | A mutation has occurred on Chromosome 17. What is the medical relevance of this mutation? | Benign | CTCTCTGGGTCTCTAGAAAGAAAGGGTAGGTCACAGAGTAACTTCACCTGCTAATTTATATTTGGGAAATGTTTGAATGTTTTATAACAAGCATACATTTCTTTAACTTTTAATTACAGTTTCTTTAAAAATATCAAATAGAACTAAAAAGCTGGCCAGGCGCGGTGGCTCACCGCTGTAATCCCAGTACTTTGGGAGGCCGAGGGGGGTGGATCACTGGAGCTCAGGAGTTCGAGACCAGCCTGGCCAACAAGGGTTAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGCATCATTGTGGGCACCTGTAATCC... | CTCTCTGGGTCTCTAGAAAGAAAGGGTAGGTCACAGAGTAACTTCACCTGCTAATTTATATTTGGGAAATGTTTGAATGTTTTATAACAAGCATACATTTCTTTAACTTTTAATTACAGTTTCTTTAAAAATATCAAATAGAACTAAAAAGCTGGCCAGGCGCGGTGGCTCACCGCTGTAATCCCAGTACTTTGGGAGGCCGAGGGGGGTGGATCACTGGAGCTCAGGAGTTCGAGACCAGCCTGGCCAACAAGGGTTAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGCATCATTGTGGGCACCTGTAATCC... |
Task1_train_45267 | This mutation on Chromosome 17 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | TTTGGGAGGCTGAGGCAGGAGGATCCCTTGAGCTCAGGAGTTCAAGACCAGCCTGGGCAACATAGTGAGACAATGTCTCTATTTAAAAAAAAAAATTTTTTTTTGGATGGAGTTTCACTCTTGTTGCCCAGGCTGGAGTGTAGTGGCGCAATCTCAGTCCACTGCAACCTCCACCTCCCCGGTTCAAGTGATTCTCCTGCCTCAGCCTCCGGAGTAGCTGGGATTACAGGCACCCGCCACCATGCCCTGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGCAGGTCTTGAACTCCTGACCT... | TTTGGGAGGCTGAGGCAGGAGGATCCCTTGAGCTCAGGAGTTCAAGACCAGCCTGGGCAACATAGTGAGACAATGTCTCTATTTAAAAAAAAAAATTTTTTTTTGGATGGAGTTTCACTCTTGTTGCCCAGGCTGGAGTGTAGTGGCGCAATCTCAGTCCACTGCAACCTCCACCTCCCCGGTTCAAGTGATTCTCCTGCCTCAGCCTCCGGAGTAGCTGGGATTACAGGCACCCGCCACCATGCCCTGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGCAGGTCTTGAACTCCTGACCT... |
Task1_train_45268 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | GCAGAGGAATGGGATGGAACAAGATGTTCTCTGACTTAGAAGATGGGCGTGCTGGGCCAGGCGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGACATGGGCAGATCACCTGAGGTCAGGAGTTTGAGACAAGCCTGGCCAACTTGGCGAAACCCCATCTCTACTGAAAATACAAAAATTAGCCAGGCCTGGTGGCAGGTTCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGTAAAGGTTGCAGTGAGCTGAGATCGCACCACCGCACTCTCCTGCCTGGGTGAC... | GCAGAGGAATGGGATGGAACAAGATGTTCTCTGACTTAGAAGATGGGCGTGCTGGGCCAGGCGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGACATGGGCAGATCACCTGAGGTCAGGAGTTTGAGACAAGCCTGGCCAACTTGGCGAAACCCCATCTCTACTGAAAATACAAAAATTAGCCAGGCCTGGTGGCAGGTTCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGTAAAGGTTGCAGTGAGCTGAGATCGCACCACCGCACTCTCCTGCCTGGGTGAC... |
Task1_train_45269 | This genomic variant is located on Chromosome 17. Can you determine its pathogenicity and name any linked disease? | Benign | TAGATGCCACTTGTTGAGATTGTTCTAGAGAGGACTCGGCCAGTGGATAGGGAGTAAAAATAGACTTCTAAATTCCTTTCAATTTTAAGATTCTTTTACTTGATCTGTGATCTCCGGTTTCTCCATTAGTCCTCTGCAGCATCCCTTTGTGGTAATGTAATATTATAGAAGTAAATTGTTGTGGGGCAACTGCAAGTGATTTCAGGAAGTAACTTCAGGTAAAGGTTGTTACAGAACACATTTCTTTGTCTTGGAATTCATGCATCTCCAAACGATAAGGCCATAGTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGA... | TAGATGCCACTTGTTGAGATTGTTCTAGAGAGGACTCGGCCAGTGGATAGGGAGTAAAAATAGACTTCTAAATTCCTTTCAATTTTAAGATTCTTTTACTTGATCTGTGATCTCCGGTTTCTCCATTAGTCCTCTGCAGCATCCCTTTGTGGTAATGTAATATTATAGAAGTAAATTGTTGTGGGGCAACTGCAAGTGATTTCAGGAAGTAACTTCAGGTAAAGGTTGTTACAGAACACATTTCTTTGTCTTGGAATTCATGCATCTCCAAACGATAAGGCCATAGTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGA... |
Task1_train_45270 | This alteration occurs on Chromosome 17. Is it associated with a disease or is it a benign variant? | Benign | GATAGAATTCCACCTTGTGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGCAGATCACTTGAGGTCAGGAGTTCGAGATCAGCCTGACCCACATGGTAAAACCCTATCTCTACTAAAGACACACACACACACACACACACACACACACACAGTCACACACACAAAGCCGGGCGTGGTTCACATGCCTGTAGTCCCAGCTACCCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATTGTGCTACTGCACTCCAGCCTGGGTGACACAG... | GATAGAATTCCACCTTGTGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGCAGATCACTTGAGGTCAGGAGTTCGAGATCAGCCTGACCCACATGGTAAAACCCTATCTCTACTAAAGACACACACACACACACACACACACACACACACAGTCACACACACAAAGCCGGGCGTGGTTCACATGCCTGTAGTCCCAGCTACCCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATTGTGCTACTGCACTCCAGCCTGGGTGACACAG... |
Task1_train_45271 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | TCTTTACCTCCGCGTTTATCCTACCCTACCGTGATGATTTGTTTTTGTCTCTTTCTAAACTGTTTCCCTCTGTGTGTCCTCACTACCTGGCATAGTGCCAGACACACAATAGTTGCTCAATAAATGTGTTGACTGGCTGTTGCAGAAACCCACTGGCACTTTGTCTATTCCCCAAATCTTACATTGCTTCAAATATTGGTTTACGACGTACCCTCTGGGCATGTGGTAAAGGGGGCATCTGACAGGGTCTGGCTGTTGCTCCTGGTGGCTGGACAGGGGTTGCTGGGAGAAGCAGCTCCAGGTTGAACGGAGTTCTGGTG... | TCTTTACCTCCGCGTTTATCCTACCCTACCGTGATGATTTGTTTTTGTCTCTTTCTAAACTGTTTCCCTCTGTGTGTCCTCACTACCTGGCATAGTGCCAGACACACAATAGTTGCTCAATAAATGTGTTGACTGGCTGTTGCAGAAACCCACTGGCACTTTGTCTATTCCCCAAATCTTACATTGCTTCAAATATTGGTTTACGACGTACCCTCTGGGCATGTGGTAAAGGGGGCATCTGACAGGGTCTGGCTGTTGCTCCTGGTGGCTGGACAGGGGTTGCTGGGAGAAGCAGCTCCAGGTTGAACGGAGTTCTGGTG... |
Task1_train_45272 | A variant was discovered on Chromosome 17. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | ATTCTTTGCAGAGGATCACCTCACCACCTTATTGTTATAAAAATTTTAGAATGGCTCTTGCTTAGAATTACATATCATATGTACTTTCTGCACATATAAAGTTGGTTTTTGGCCAGGCGTGGTGGCTCATGCCTGTAATGTCGGCACTTTGGGAGGCTGAGGCAGGAGGATCACTTCAGGCCAGGAGTTGGAGACCAGCCTGGGCAACATATTGAGACCCTGTCTCTATTTTTATTTTTAAAAAATTGGTTTTCAATGAAATAGTTTCCTCCAGTTGCTACTACTGTGAGATTATGAAGCTCATTTCAAGATGCTCCTGT... | ATTCTTTGCAGAGGATCACCTCACCACCTTATTGTTATAAAAATTTTAGAATGGCTCTTGCTTAGAATTACATATCATATGTACTTTCTGCACATATAAAGTTGGTTTTTGGCCAGGCGTGGTGGCTCATGCCTGTAATGTCGGCACTTTGGGAGGCTGAGGCAGGAGGATCACTTCAGGCCAGGAGTTGGAGACCAGCCTGGGCAACATATTGAGACCCTGTCTCTATTTTTATTTTTAAAAAATTGGTTTTCAATGAAATAGTTTCCTCCAGTTGCTACTACTGTGAGATTATGAAGCTCATTTCAAGATGCTCCTGT... |
Task1_train_45273 | Assess the clinical impact of this variant found on Chromosome 17. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | GCATAAGTAGTGCAAGCTGACTCCGAGCACATCCAGGAATGCGCTTACTGATGAGATATCGAGGCAAGCTAAATCAGCAGTTCCTGAGGACGCGCTTGGGGGATGGCACCCAAAGCCCCTGCATTATCTCTTTGTGATAGTTTGAGCCCCTGCACCTGGAACTGTTTACTTTTCTGTAACTGTTTCTGTAACCAATTAATCTTTCTTAATTGGTTTGCCTGTTCTGCTTCTGTAAAAATTGCTTCAGCTAAACTCCCTCTCCCCTATTTAGACCACGATATAAAAAGAAATCTAGCCCCTTCTTCGGGGCCGAGAGAATT... | GCATAAGTAGTGCAAGCTGACTCCGAGCACATCCAGGAATGCGCTTACTGATGAGATATCGAGGCAAGCTAAATCAGCAGTTCCTGAGGACGCGCTTGGGGGATGGCACCCAAAGCCCCTGCATTATCTCTTTGTGATAGTTTGAGCCCCTGCACCTGGAACTGTTTACTTTTCTGTAACTGTTTCTGTAACCAATTAATCTTTCTTAATTGGTTTGCCTGTTCTGCTTCTGTAAAAATTGCTTCAGCTAAACTCCCTCTCCCCTATTTAGACCACGATATAAAAAGAAATCTAGCCCCTTCTTCGGGGCCGAGAGAATT... |
Task1_train_45274 | This variant is found on Chromosome 17. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GGATTACAGGCATGAGCCACTGTGCCCAGCCTCCAGCTAATTTTTTAAAAATTATTTTTTGAAGAGGAAGGGGTTTTGCTATGTTGCTCAAGCTGGTCTTGAACTCCTGGGCTCACGTGATTCTCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCCTGAGCCACTGCACGCAGCCTGTGTCTGTTACTTTATTACTCTCTATATATACAAGTCTAAGCCCTGAGTCCCATTTTGGTTTTATAAAATAAATTCACTAAGGTATGCATTTTAGTTTGTTCATGACTTTGGTTTACCCTCCCTCTCCATCGAGCAGGC... | GGATTACAGGCATGAGCCACTGTGCCCAGCCTCCAGCTAATTTTTTAAAAATTATTTTTTGAAGAGGAAGGGGTTTTGCTATGTTGCTCAAGCTGGTCTTGAACTCCTGGGCTCACGTGATTCTCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCCTGAGCCACTGCACGCAGCCTGTGTCTGTTACTTTATTACTCTCTATATATACAAGTCTAAGCCCTGAGTCCCATTTTGGTTTTATAAAATAAATTCACTAAGGTATGCATTTTAGTTTGTTCATGACTTTGGTTTACCCTCCCTCTCCATCGAGCAGGC... |
Task1_train_45275 | This mutation occurs on Chromosome 17. Does this change lead to a known medical condition, or is it benign? | Benign | TGGTATAATAGTTTAACTTCATGCTCATTATTTTTACAGCCAGACCTATTAAGAATATGTACTAGCGTTAAGTATGTATACTTAATGTGTGTATGAAGTAAATGTTTTAGTGTTTTAAATCTGCCACTGTCATTTAGAAATTGAGATCTAGTTTTCTAGTTTAAGGATGGCCTTAAAGTATATTTATTTTATATTTATTTTATCTAATTAGACTTAATGTCCAAAGCGGATCATTTTAACTTAGTTATAATTACACAGCCAAACACTGCTCTTATAACCCTGATTGGTCTGGAAAACATGATTCGTTTTTTTTTTTCCCC... | TGGTATAATAGTTTAACTTCATGCTCATTATTTTTACAGCCAGACCTATTAAGAATATGTACTAGCGTTAAGTATGTATACTTAATGTGTGTATGAAGTAAATGTTTTAGTGTTTTAAATCTGCCACTGTCATTTAGAAATTGAGATCTAGTTTTCTAGTTTAAGGATGGCCTTAAAGTATATTTATTTTATATTTATTTTATCTAATTAGACTTAATGTCCAAAGCGGATCATTTTAACTTAGTTATAATTACACAGCCAAACACTGCTCTTATAACCCTGATTGGTCTGGAAAACATGATTCGTTTTTTTTTTTCCCC... |
Task1_train_45276 | A variant affecting Chromosome 17 has been observed. Determine if it's benign or associated with disease. | Benign | CAGCCAGACCTATTAAGAATATGTACTAGCGTTAAGTATGTATACTTAATGTGTGTATGAAGTAAATGTTTTAGTGTTTTAAATCTGCCACTGTCATTTAGAAATTGAGATCTAGTTTTCTAGTTTAAGGATGGCCTTAAAGTATATTTATTTTATATTTATTTTATCTAATTAGACTTAATGTCCAAAGCGGATCATTTTAACTTAGTTATAATTACACAGCCAAACACTGCTCTTATAACCCTGATTGGTCTGGAAAACATGATTCGTTTTTTTTTTTCCCCATAGGAAACTTGATGAGAGAGCAAGGGTGAATCTGT... | CAGCCAGACCTATTAAGAATATGTACTAGCGTTAAGTATGTATACTTAATGTGTGTATGAAGTAAATGTTTTAGTGTTTTAAATCTGCCACTGTCATTTAGAAATTGAGATCTAGTTTTCTAGTTTAAGGATGGCCTTAAAGTATATTTATTTTATATTTATTTTATCTAATTAGACTTAATGTCCAAAGCGGATCATTTTAACTTAGTTATAATTACACAGCCAAACACTGCTCTTATAACCCTGATTGGTCTGGAAAACATGATTCGTTTTTTTTTTTCCCCATAGGAAACTTGATGAGAGAGCAAGGGTGAATCTGT... |
Task1_train_45277 | Mutation context: Chromosome 17. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | ATTCACACATATATTCAATTCAATGGCGATTCCTACGTACCACAGCCATGAGGGACTGAAGTTCTATTTCCAGGGTTTGCAGATTGCGTTTTAATTCGGTCAGCTCATTTCTGGCTGCTGTGGCTGCTCCCTCATGATCGGAAATCTGTTGTTGCAGCGTTGCACTCTGAAGTGTAATTGTCGAAAGGGTTAGTGACTGGCCTGATTGTCTCCTGAGCAAGCCCTTTGTAATTTGCCATAGACCTACCCTCTCGTTGAACCAGGCTTCAGCATCTTTGCGGTTCTGCTCAGCCAAGTCCTCATACTCAGCCCTCATGTTG... | ATTCACACATATATTCAATTCAATGGCGATTCCTACGTACCACAGCCATGAGGGACTGAAGTTCTATTTCCAGGGTTTGCAGATTGCGTTTTAATTCGGTCAGCTCATTTCTGGCTGCTGTGGCTGCTCCCTCATGATCGGAAATCTGTTGTTGCAGCGTTGCACTCTGAAGTGTAATTGTCGAAAGGGTTAGTGACTGGCCTGATTGTCTCCTGAGCAAGCCCTTTGTAATTTGCCATAGACCTACCCTCTCGTTGAACCAGGCTTCAGCATCTTTGCGGTTCTGCTCAGCCAAGTCCTCATACTCAGCCCTCATGTTG... |
Task1_train_45278 | A variant found on Chromosome 17 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GACCCATCTTCTCCATCTATCAGGAGGCAGTAGGTCTCAATTTCTTTTTCCAGGTGGACCTTGATGTCAAGGAGCTGCTCATACTCGAGCTTCTGGCCCTCGGTCTCGGTTCTGACCTGGTGCAGCTGCTCCTCCAGGGCCCCGATCTGAGCCTGGATCTGTGCCAGCTGTGCACAGTAGTTACTCTCGGTCTCTGTCAAGGAGCACTCCAGGGAGTGTTTCTGTAGTTTGGTAAGACATGGTTTAATAGAAAAGGTCACGGTGTTTTAGAATAAGCCAAAGCATTTAAGAGATAATTAAGAGAATTATCCTTACATCAT... | GACCCATCTTCTCCATCTATCAGGAGGCAGTAGGTCTCAATTTCTTTTTCCAGGTGGACCTTGATGTCAAGGAGCTGCTCATACTCGAGCTTCTGGCCCTCGGTCTCGGTTCTGACCTGGTGCAGCTGCTCCTCCAGGGCCCCGATCTGAGCCTGGATCTGTGCCAGCTGTGCACAGTAGTTACTCTCGGTCTCTGTCAAGGAGCACTCCAGGGAGTGTTTCTGTAGTTTGGTAAGACATGGTTTAATAGAAAAGGTCACGGTGTTTTAGAATAAGCCAAAGCATTTAAGAGATAATTAAGAGAATTATCCTTACATCAT... |
Task1_train_45279 | This alteration occurs on Chromosome 17. Is it associated with a disease or is it a benign variant? | Benign | TTTTTTATATAAAGTCTTGATTTTATATACATTCATAGCCTCATCTGTGGATAAACTCTGGTGGTTTACTAGCCATAGTGGGAAAAGTATAGACTTGGGAGTTAGAAAATTTGGAGAGAACTTCTGGATTCCTTCATACCCAACTGTGGGACTGTGGGAATTGCTTAACTTCTTCGAATCTCAGAGTCCTCTTTTGGAAATAATGACATGAGTTATAACGTCTGCCCTGCCCATGCCCCGGGGTTGTTGTGGACTCACATGTGGGCGGAAGTGCTGGGCAAACCCTTAATGAAAGCAGTTATGATTATCATTACACATGT... | TTTTTTATATAAAGTCTTGATTTTATATACATTCATAGCCTCATCTGTGGATAAACTCTGGTGGTTTACTAGCCATAGTGGGAAAAGTATAGACTTGGGAGTTAGAAAATTTGGAGAGAACTTCTGGATTCCTTCATACCCAACTGTGGGACTGTGGGAATTGCTTAACTTCTTCGAATCTCAGAGTCCTCTTTTGGAAATAATGACATGAGTTATAACGTCTGCCCTGCCCATGCCCCGGGGTTGTTGTGGACTCACATGTGGGCGGAAGTGCTGGGCAAACCCTTAATGAAAGCAGTTATGATTATCATTACACATGT... |
Task1_train_45280 | This variant is present on Chromosome 17. Is the change likely to result in a pathogenic outcome? | Benign | AGCTTCTACCTCCTCATGATTCTTCTTGAGGTAAGCGAGCTCCTCACTGAGAGTTTCCAGCTGGATCTCCAGGTCCGTTCTGCACAAGGTCAGCTCATCCAGGACTCTTCGCAAACCATTGATGTCCGCCTCCACGCTCTGGTGAAGCGCTAGCTCGTTTTCAAACCTTAGAAAAGTATTTGGAAGTTTCATCATTAGTCATTAGACATGGCACATCACTTTTTAGATCATCATACAACTCAGACTAAGCTTTGAGGTAAAACTACTAAGATAATACTTAAAACTTCAGGCCGGGCGCGGTGGCTCACGCCTGTAATCCC... | AGCTTCTACCTCCTCATGATTCTTCTTGAGGTAAGCGAGCTCCTCACTGAGAGTTTCCAGCTGGATCTCCAGGTCCGTTCTGCACAAGGTCAGCTCATCCAGGACTCTTCGCAAACCATTGATGTCCGCCTCCACGCTCTGGTGAAGCGCTAGCTCGTTTTCAAACCTTAGAAAAGTATTTGGAAGTTTCATCATTAGTCATTAGACATGGCACATCACTTTTTAGATCATCATACAACTCAGACTAAGCTTTGAGGTAAAACTACTAAGATAATACTTAAAACTTCAGGCCGGGCGCGGTGGCTCACGCCTGTAATCCC... |
Task1_train_45281 | Here is a genetic alteration on Chromosome 17. Based on the data, is it a benign variant or a cause of disease? | Benign | ATTGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCTGAGATTGCGCCACTGCACTCCAGCCTGGCCACAGAGCGAGACTCTGTCTCAAAACAAAGCAATAGAAAACAAACAAAAAAAATTAGGGACCTGTTAATTAAAATTACCACCACCACCAAAAACAGTCATAGCACCCCAAGAGAAGTAATTTATTCTTTTAAATGAGAAAGGGATTTAAAGACCGGAGAGTTACTCAACATATAGTTACTGACTAAATGTCAGGTTGATGGGAATAGAACAGTAGAAAAAATCCTGAAATCCTGGCCCTCATAGGCATTCATCC... | ATTGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCTGAGATTGCGCCACTGCACTCCAGCCTGGCCACAGAGCGAGACTCTGTCTCAAAACAAAGCAATAGAAAACAAACAAAAAAAATTAGGGACCTGTTAATTAAAATTACCACCACCACCAAAAACAGTCATAGCACCCCAAGAGAAGTAATTTATTCTTTTAAATGAGAAAGGGATTTAAAGACCGGAGAGTTACTCAACATATAGTTACTGACTAAATGTCAGGTTGATGGGAATAGAACAGTAGAAAAAATCCTGAAATCCTGGCCCTCATAGGCATTCATCC... |
Task1_train_45282 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | GTGAGCTGAGATTGCGCCACTGCACTCCAGCCTGGCCACAGAGCGAGACTCTGTCTCAAAACAAAGCAATAGAAAACAAACAAAAAAAATTAGGGACCTGTTAATTAAAATTACCACCACCACCAAAAACAGTCATAGCACCCCAAGAGAAGTAATTTATTCTTTTAAATGAGAAAGGGATTTAAAGACCGGAGAGTTACTCAACATATAGTTACTGACTAAATGTCAGGTTGATGGGAATAGAACAGTAGAAAAAATCCTGAAATCCTGGCCCTCATAGGCATTCATCCTAGGGATGACCGCTGTCATTTATTGAGTGA... | GTGAGCTGAGATTGCGCCACTGCACTCCAGCCTGGCCACAGAGCGAGACTCTGTCTCAAAACAAAGCAATAGAAAACAAACAAAAAAAATTAGGGACCTGTTAATTAAAATTACCACCACCACCAAAAACAGTCATAGCACCCCAAGAGAAGTAATTTATTCTTTTAAATGAGAAAGGGATTTAAAGACCGGAGAGTTACTCAACATATAGTTACTGACTAAATGTCAGGTTGATGGGAATAGAACAGTAGAAAAAATCCTGAAATCCTGGCCCTCATAGGCATTCATCCTAGGGATGACCGCTGTCATTTATTGAGTGA... |
Task1_train_45283 | This variant is located on Chromosome 17. Evaluate its biological effect and specify any disease association. | Benign | TTTTGCTGTTGTGTTTTTCCTTTCCTTTTTTCCCACCATTGTTTACTGTTCAGTTGGGGAGGAGAAGAAAAGTGAATAAATTATAAGGCAATACTTTCCTACCAGCGATGAATCCCAATACCACAGCATCCCAGGGAATAATTTTCCCTTTGGCTGGCTGCCGTGGCTGTAAATAGCAGCAGCCCCTCTCTAAGTGGAATTTCTAAAAGCCGTTGAAAATAAGTTACTCTTTTTGCTTAACGTTCTTCATGATTTAACTTAAAACACTGATACTTCTTTAGTGGCTTTGACTAAGATTTTACAGGTTCAGAACCATGGCC... | TTTTGCTGTTGTGTTTTTCCTTTCCTTTTTTCCCACCATTGTTTACTGTTCAGTTGGGGAGGAGAAGAAAAGTGAATAAATTATAAGGCAATACTTTCCTACCAGCGATGAATCCCAATACCACAGCATCCCAGGGAATAATTTTCCCTTTGGCTGGCTGCCGTGGCTGTAAATAGCAGCAGCCCCTCTCTAAGTGGAATTTCTAAAAGCCGTTGAAAATAAGTTACTCTTTTTGCTTAACGTTCTTCATGATTTAACTTAAAACACTGATACTTCTTTAGTGGCTTTGACTAAGATTTTACAGGTTCAGAACCATGGCC... |
Task1_train_45284 | A genomic change on Chromosome 17 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CAGACTGGAGTGCAATGGTACGATCTCGGCTCACTGTAACCTCTGCCTCCCAGGTTCAAGCAATTATCCTGCCTCAGCCTCCCGAGTAGCTGGGGTTACAGGCATCCGCCACCATGCCCGGCTAATTTTTGCATTTTTAGTAGAGACAGCATTTTGCCATGTTGGCCAGGCTGGTCTTGAAGTTCTGACCTCAGGTGATCTGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTGCCCGGCCAAGAATGACATTTTCAACTGGATAGGAGTTTACAAGGATTTAGTTTATCCCCAGCTACAGTG... | CAGACTGGAGTGCAATGGTACGATCTCGGCTCACTGTAACCTCTGCCTCCCAGGTTCAAGCAATTATCCTGCCTCAGCCTCCCGAGTAGCTGGGGTTACAGGCATCCGCCACCATGCCCGGCTAATTTTTGCATTTTTAGTAGAGACAGCATTTTGCCATGTTGGCCAGGCTGGTCTTGAAGTTCTGACCTCAGGTGATCTGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTGCCCGGCCAAGAATGACATTTTCAACTGGATAGGAGTTTACAAGGATTTAGTTTATCCCCAGCTACAGTG... |
Task1_train_45285 | This alteration on Chromosome 17 may affect genome function. Does it lead to a disease or is it benign? | Benign | ATTGAGTTCAAGTCCCAGTTCTGTTTGCATGTAACACCTGCTTTTCTGAAGCGCATAATTTTAACCTTAAAGAGAATCTCCTAACTGTGCTGGATACTCTCCCTTTATCGTGGCTGCTAATTTTCAGGGGGCCGTTCATGCTGCCTGGCGGTTAAAGCACATTTCCCTGGTCAGCCAGTCTCCTACTCTCCCAGGAGGTTATTTTGTTCCCTCTCCTCTGTCCTTGCCATCCTTCCTCGGAGTCCATGGCCTCGCTTCCTAATTTTGTTGATGAAATGAAAGCAATCGGGAGAGACCGCCCACTGCTCCCTACATTGCTC... | ATTGAGTTCAAGTCCCAGTTCTGTTTGCATGTAACACCTGCTTTTCTGAAGCGCATAATTTTAACCTTAAAGAGAATCTCCTAACTGTGCTGGATACTCTCCCTTTATCGTGGCTGCTAATTTTCAGGGGGCCGTTCATGCTGCCTGGCGGTTAAAGCACATTTCCCTGGTCAGCCAGTCTCCTACTCTCCCAGGAGGTTATTTTGTTCCCTCTCCTCTGTCCTTGCCATCCTTCCTCGGAGTCCATGGCCTCGCTTCCTAATTTTGTTGATGAAATGAAAGCAATCGGGAGAGACCGCCCACTGCTCCCTACATTGCTC... |
Task1_train_45286 | A mutation has occurred on Chromosome 17. What is the medical relevance of this mutation? | Benign | GCCCTTCTGCAAAGCACCTTACAGTTTATGAGACCCTTTCACCATTATTATTCCATTTTATCCTTGCAGCCGTGTGGTAGGCAGGGCTTATATTGTTATATCCTATTTACTCGAGGTCATACATGCCCAGGCTGGATTGAGACTCCGTCCCAAGGTTTCTGAATCCCAGTTCCATGCTCTTTCCACATTTTCATCCTGCAGCCTGAGATAGTACGCAGTTAACTACTGACCGGAGGTACTCTGCCCACTCAGATGAGAGAGAAATTATTGATTTAAAAGAGGTCATTCTGGGAGTTCTGCATTCCACTTGCCTAGTGTAA... | GCCCTTCTGCAAAGCACCTTACAGTTTATGAGACCCTTTCACCATTATTATTCCATTTTATCCTTGCAGCCGTGTGGTAGGCAGGGCTTATATTGTTATATCCTATTTACTCGAGGTCATACATGCCCAGGCTGGATTGAGACTCCGTCCCAAGGTTTCTGAATCCCAGTTCCATGCTCTTTCCACATTTTCATCCTGCAGCCTGAGATAGTACGCAGTTAACTACTGACCGGAGGTACTCTGCCCACTCAGATGAGAGAGAAATTATTGATTTAAAAGAGGTCATTCTGGGAGTTCTGCATTCCACTTGCCTAGTGTAA... |
Task1_train_45287 | A genomic variant on Chromosome 17 is under review. What is the biological outcome — benign or pathogenic? | Benign | GTGAGTTAGGGAAGGAGCAGAATAAAAGATATTCTACCTAGCAATGGGGACCCGCTGTAGTAGTAAGAAACTAAGTACCTTAAGGGACTGGGGAGTTTTCTTAAACCTCTCTGGCAGGAGCATGTATTGGCCTCTGTTTCATAAATGTGGGTCATTTTCATCACCTTGGGATGTTAGACTTTGGCAGGTCTGATGATGAAACAAGGCTGCACATGCTCGTAAGAAGAAATGACCTTCCCATCCTTAATCTCCTTGGTGATGGTGCAAATTTTAACCAGTATCCGGGACAGGGGTCCGCAGGCACTGCAGTGCTCCTTTAA... | GTGAGTTAGGGAAGGAGCAGAATAAAAGATATTCTACCTAGCAATGGGGACCCGCTGTAGTAGTAAGAAACTAAGTACCTTAAGGGACTGGGGAGTTTTCTTAAACCTCTCTGGCAGGAGCATGTATTGGCCTCTGTTTCATAAATGTGGGTCATTTTCATCACCTTGGGATGTTAGACTTTGGCAGGTCTGATGATGAAACAAGGCTGCACATGCTCGTAAGAAGAAATGACCTTCCCATCCTTAATCTCCTTGGTGATGGTGCAAATTTTAACCAGTATCCGGGACAGGGGTCCGCAGGCACTGCAGTGCTCCTTTAA... |
Task1_train_45288 | A genetic alteration is present on Chromosome 17. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GTTTGTTTGTTTGTTTTGTCTGCACCTGTTGGTGTTTCTGGTTGTTGGTTTCTCCAGCTCCCCCTCTGGGATATATGAGATAAAAAGCTAATCCAGGGAGCTCACCACAGTGTCACTCCTGGAGTCTCAACATCTTTAGGTGGTTTGGCTTCTTCTTCTACCTTTCAGAGTCCTCTTATGTTTATTTGATATGTAATTTCCAGGGTTTTTAGGAGGAGGAATATGGAAATATACATCATTCTGGAAGTTCTCTACCTTGTTTTTTAAATATATGAGAATAATTATTCTTATAACCTAAATGTCCAATAACAGATCAATGT... | GTTTGTTTGTTTGTTTTGTCTGCACCTGTTGGTGTTTCTGGTTGTTGGTTTCTCCAGCTCCCCCTCTGGGATATATGAGATAAAAAGCTAATCCAGGGAGCTCACCACAGTGTCACTCCTGGAGTCTCAACATCTTTAGGTGGTTTGGCTTCTTCTTCTACCTTTCAGAGTCCTCTTATGTTTATTTGATATGTAATTTCCAGGGTTTTTAGGAGGAGGAATATGGAAATATACATCATTCTGGAAGTTCTCTACCTTGTTTTTTAAATATATGAGAATAATTATTCTTATAACCTAAATGTCCAATAACAGATCAATGT... |
Task1_train_45289 | A variant has been detected on Chromosome 17. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TTTGTTTGTTTTGTCTGCACCTGTTGGTGTTTCTGGTTGTTGGTTTCTCCAGCTCCCCCTCTGGGATATATGAGATAAAAAGCTAATCCAGGGAGCTCACCACAGTGTCACTCCTGGAGTCTCAACATCTTTAGGTGGTTTGGCTTCTTCTTCTACCTTTCAGAGTCCTCTTATGTTTATTTGATATGTAATTTCCAGGGTTTTTAGGAGGAGGAATATGGAAATATACATCATTCTGGAAGTTCTCTACCTTGTTTTTTAAATATATGAGAATAATTATTCTTATAACCTAAATGTCCAATAACAGATCAATGTACCTT... | TTTGTTTGTTTTGTCTGCACCTGTTGGTGTTTCTGGTTGTTGGTTTCTCCAGCTCCCCCTCTGGGATATATGAGATAAAAAGCTAATCCAGGGAGCTCACCACAGTGTCACTCCTGGAGTCTCAACATCTTTAGGTGGTTTGGCTTCTTCTTCTACCTTTCAGAGTCCTCTTATGTTTATTTGATATGTAATTTCCAGGGTTTTTAGGAGGAGGAATATGGAAATATACATCATTCTGGAAGTTCTCTACCTTGTTTTTTAAATATATGAGAATAATTATTCTTATAACCTAAATGTCCAATAACAGATCAATGTACCTT... |
Task1_train_45290 | Chromosome 17 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GTCTCAACATCTTTAGGTGGTTTGGCTTCTTCTTCTACCTTTCAGAGTCCTCTTATGTTTATTTGATATGTAATTTCCAGGGTTTTTAGGAGGAGGAATATGGAAATATACATCATTCTGGAAGTTCTCTACCTTGTTTTTTAAATATATGAGAATAATTATTCTTATAACCTAAATGTCCAATAACAGATCAATGTACCTTATGGTACATTATGCAACCAGTAAAATGATGGCTACAGGCTGGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAAGCTGGTGGATCACAAGGTCAAGAGATTGAGA... | GTCTCAACATCTTTAGGTGGTTTGGCTTCTTCTTCTACCTTTCAGAGTCCTCTTATGTTTATTTGATATGTAATTTCCAGGGTTTTTAGGAGGAGGAATATGGAAATATACATCATTCTGGAAGTTCTCTACCTTGTTTTTTAAATATATGAGAATAATTATTCTTATAACCTAAATGTCCAATAACAGATCAATGTACCTTATGGTACATTATGCAACCAGTAAAATGATGGCTACAGGCTGGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAAGCTGGTGGATCACAAGGTCAAGAGATTGAGA... |
Task1_train_45291 | A mutation found on Chromosome 17 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CTGCTGTCCTCGCTGTCCAGCAGGCCCCAGTACGTGTTGATCTCACCCTCCAGCCGGGCCTTCACGTCCAGGAGCACCTGGTACTCCTGGTTCTGTCGCTCCAGGTCGCAGCGGATCTCGGCCAGCTGGTTCTCCAGGTTATCGATCAGACACTGAATTTGGGCCAGCTGGGAGCTGTACTGGGCCTCGGTTTCTGCCACGGTGCATTCCAGAGATTCTGTCTGCGGGAGGAAACATTGTCCAAAGGACCATGAAGTGCAGTCTCTCGGGCCAGAGTGCCTACTTTCAAATTCCTGCTTACCCTTTTCTAGCTATGTGAC... | CTGCTGTCCTCGCTGTCCAGCAGGCCCCAGTACGTGTTGATCTCACCCTCCAGCCGGGCCTTCACGTCCAGGAGCACCTGGTACTCCTGGTTCTGTCGCTCCAGGTCGCAGCGGATCTCGGCCAGCTGGTTCTCCAGGTTATCGATCAGACACTGAATTTGGGCCAGCTGGGAGCTGTACTGGGCCTCGGTTTCTGCCACGGTGCATTCCAGAGATTCTGTCTGCGGGAGGAAACATTGTCCAAAGGACCATGAAGTGCAGTCTCTCGGGCCAGAGTGCCTACTTTCAAATTCCTGCTTACCCTTTTCTAGCTATGTGAC... |
Task1_train_45292 | A genetic alteration is present on Chromosome 17. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | CAGCCGGGCCTTCACGTCCAGGAGCACCTGGTACTCCTGGTTCTGTCGCTCCAGGTCGCAGCGGATCTCGGCCAGCTGGTTCTCCAGGTTATCGATCAGACACTGAATTTGGGCCAGCTGGGAGCTGTACTGGGCCTCGGTTTCTGCCACGGTGCATTCCAGAGATTCTGTCTGCGGGAGGAAACATTGTCCAAAGGACCATGAAGTGCAGTCTCTCGGGCCAGAGTGCCTACTTTCAAATTCCTGCTTACCCTTTTCTAGCTATGTGACCACTGGCAAATTATTTAGCTTCTGTGAGTCTCAGTTTTATTCTCTGTATA... | CAGCCGGGCCTTCACGTCCAGGAGCACCTGGTACTCCTGGTTCTGTCGCTCCAGGTCGCAGCGGATCTCGGCCAGCTGGTTCTCCAGGTTATCGATCAGACACTGAATTTGGGCCAGCTGGGAGCTGTACTGGGCCTCGGTTTCTGCCACGGTGCATTCCAGAGATTCTGTCTGCGGGAGGAAACATTGTCCAAAGGACCATGAAGTGCAGTCTCTCGGGCCAGAGTGCCTACTTTCAAATTCCTGCTTACCCTTTTCTAGCTATGTGACCACTGGCAAATTATTTAGCTTCTGTGAGTCTCAGTTTTATTCTCTGTATA... |
Task1_train_45293 | This variant is found on Chromosome 17. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | CTGCCACGGTGCATTCCAGAGATTCTGTCTGCGGGAGGAAACATTGTCCAAAGGACCATGAAGTGCAGTCTCTCGGGCCAGAGTGCCTACTTTCAAATTCCTGCTTACCCTTTTCTAGCTATGTGACCACTGGCAAATTATTTAGCTTCTGTGAGTCTCAGTTTTATTCTCTGTATAGTGGAGAATACAAAGTATCTGTTTCATTAGACGGTTGTGAAGATTAAGAGTTAATATGCGGGCTGGGCGCGGTGGCTCAGGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACAAGGTCAGAAGATCGAGAC... | CTGCCACGGTGCATTCCAGAGATTCTGTCTGCGGGAGGAAACATTGTCCAAAGGACCATGAAGTGCAGTCTCTCGGGCCAGAGTGCCTACTTTCAAATTCCTGCTTACCCTTTTCTAGCTATGTGACCACTGGCAAATTATTTAGCTTCTGTGAGTCTCAGTTTTATTCTCTGTATAGTGGAGAATACAAAGTATCTGTTTCATTAGACGGTTGTGAAGATTAAGAGTTAATATGCGGGCTGGGCGCGGTGGCTCAGGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACAAGGTCAGAAGATCGAGAC... |
Task1_train_45294 | An alteration has been detected on Chromosome 17. Is it pathogenic, and if so, what disease is involved? | Benign | TTTCAAATTCCTGCTTACCCTTTTCTAGCTATGTGACCACTGGCAAATTATTTAGCTTCTGTGAGTCTCAGTTTTATTCTCTGTATAGTGGAGAATACAAAGTATCTGTTTCATTAGACGGTTGTGAAGATTAAGAGTTAATATGCGGGCTGGGCGCGGTGGCTCAGGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACAAGGTCAGAAGATCGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATATAAAAAATTAGCTGGGTACGGTGGTGGACGCCTGTAGTCCCAGCTACT... | TTTCAAATTCCTGCTTACCCTTTTCTAGCTATGTGACCACTGGCAAATTATTTAGCTTCTGTGAGTCTCAGTTTTATTCTCTGTATAGTGGAGAATACAAAGTATCTGTTTCATTAGACGGTTGTGAAGATTAAGAGTTAATATGCGGGCTGGGCGCGGTGGCTCAGGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACAAGGTCAGAAGATCGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATATAAAAAATTAGCTGGGTACGGTGGTGGACGCCTGTAGTCCCAGCTACT... |
Task1_train_45295 | Here is a variant on Chromosome 17. Please identify whether it is a benign mutation or associated with a disorder. | Benign | CCCTGTTGAGGTCAAGGGTGGGGGCAGTGTCCAGCTCCACACTGAGGCGGTCGCCAAGCTGTTCACGAAGCAAGTTGACTTCCTGAAAGTGGGATGGTGTAAAGAATGTCACAGAATGGTGGGGAAAAATCCATTTGACATCCAATGGCATTCTACTTCTGTTTTTTGGAGCAGTGGGTAAAAGTGTGAGATTTTGATTCAGATTGCCTGGGCTGAATCTCTTTTCACCACTTAGAAGGGCCTCAGTTTCTTCGTCTGTAAAATGGACATAATAATTGGACATTTTTCCAGAAAGTTATTGTGAGATCTAGAAGAGTCAA... | CCCTGTTGAGGTCAAGGGTGGGGGCAGTGTCCAGCTCCACACTGAGGCGGTCGCCAAGCTGTTCACGAAGCAAGTTGACTTCCTGAAAGTGGGATGGTGTAAAGAATGTCACAGAATGGTGGGGAAAAATCCATTTGACATCCAATGGCATTCTACTTCTGTTTTTTGGAGCAGTGGGTAAAAGTGTGAGATTTTGATTCAGATTGCCTGGGCTGAATCTCTTTTCACCACTTAGAAGGGCCTCAGTTTCTTCGTCTGTAAAATGGACATAATAATTGGACATTTTTCCAGAAAGTTATTGTGAGATCTAGAAGAGTCAA... |
Task1_train_45296 | A variant affecting Chromosome 17 has been observed. Determine if it's benign or associated with disease. | Benign | CAGGCTGGAGTGCAGTGGTAAGATCTCGGCTCACTGCAACCTCCGCCTCCTGAGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTAGGACTACAGGCGCCTGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGAGGTTTCATCATATTGGTCAGGCTGGTCTCGAACTCCTGACCTTGTGATCCTCCTGCCTCAGCCTCCCAAAGTGCTTGGATTACAGGTGTGAGCCACCATGCCTGGCCCTGCCTCAAGTAGTTTTATTCCAGCTTAAACAACATCTGCCCAAATTCGATTTACAAACATCAA... | CAGGCTGGAGTGCAGTGGTAAGATCTCGGCTCACTGCAACCTCCGCCTCCTGAGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTAGGACTACAGGCGCCTGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGAGGTTTCATCATATTGGTCAGGCTGGTCTCGAACTCCTGACCTTGTGATCCTCCTGCCTCAGCCTCCCAAAGTGCTTGGATTACAGGTGTGAGCCACCATGCCTGGCCCTGCCTCAAGTAGTTTTATTCCAGCTTAAACAACATCTGCCCAAATTCGATTTACAAACATCAA... |
Task1_train_45297 | Located on Chromosome 17, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | GAGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTAGGACTACAGGCGCCTGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGAGGTTTCATCATATTGGTCAGGCTGGTCTCGAACTCCTGACCTTGTGATCCTCCTGCCTCAGCCTCCCAAAGTGCTTGGATTACAGGTGTGAGCCACCATGCCTGGCCCTGCCTCAAGTAGTTTTATTCCAGCTTAAACAACATCTGCCCAAATTCGATTTACAAACATCAACAGATCATCTGTCAATGTAAGTACGTTACTCTCGGAGTCCTTCAGCGGAGT... | GAGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTAGGACTACAGGCGCCTGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGAGGTTTCATCATATTGGTCAGGCTGGTCTCGAACTCCTGACCTTGTGATCCTCCTGCCTCAGCCTCCCAAAGTGCTTGGATTACAGGTGTGAGCCACCATGCCTGGCCCTGCCTCAAGTAGTTTTATTCCAGCTTAAACAACATCTGCCCAAATTCGATTTACAAACATCAACAGATCATCTGTCAATGTAAGTACGTTACTCTCGGAGTCCTTCAGCGGAGT... |
Task1_train_45298 | A mutation has occurred on Chromosome 17. What is the medical relevance of this mutation? | Benign | TCCTCCTGCCTCAGCCTCCCAAAGTGCTTGGATTACAGGTGTGAGCCACCATGCCTGGCCCTGCCTCAAGTAGTTTTATTCCAGCTTAAACAACATCTGCCCAAATTCGATTTACAAACATCAACAGATCATCTGTCAATGTAAGTACGTTACTCTCGGAGTCCTTCAGCGGAGTTGCCACTTTCCTTACCTCTTCATGGTTTTTCTTAAGGCAAAGGAGATCTTCCTTCAGAGACTCCACATGGGCCTCCAGATCAGATTTGCACAGGGTCAGTTCCTCCAGGATCCCATGCAGGCTGCTGATGTCAGCCTCTAACAGC... | TCCTCCTGCCTCAGCCTCCCAAAGTGCTTGGATTACAGGTGTGAGCCACCATGCCTGGCCCTGCCTCAAGTAGTTTTATTCCAGCTTAAACAACATCTGCCCAAATTCGATTTACAAACATCAACAGATCATCTGTCAATGTAAGTACGTTACTCTCGGAGTCCTTCAGCGGAGTTGCCACTTTCCTTACCTCTTCATGGTTTTTCTTAAGGCAAAGGAGATCTTCCTTCAGAGACTCCACATGGGCCTCCAGATCAGATTTGCACAGGGTCAGTTCCTCCAGGATCCCATGCAGGCTGCTGATGTCAGCCTCTAACAGC... |
Task1_train_45299 | A variant on Chromosome 17 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | CTCAGAGGCTTTCCGTAGCTATTTCTCACCTTTGACACTGAATCACCAAATCAGGGTTTTAGTTATTCTTTCTGTATGCTTGCATGCCATGCTGCTCACCTCCCAGTCACAGCAGAATCCCTCAGCATTGCAATTATTATTATGATAACTTGTCTTTCTTCTTCACTAGATTTGGGAGAGACTTGAGGGCACTTGAGACTTGAGGTAATAGCATTTCTTTTATCTTTTTACTCCTGGCATCAATATGATGCCTGACATAGGGCAAACACTCAGGAAATATGGACAAATGAATGAGTGAATGGACTAGATCTCTTGTTGAC... | CTCAGAGGCTTTCCGTAGCTATTTCTCACCTTTGACACTGAATCACCAAATCAGGGTTTTAGTTATTCTTTCTGTATGCTTGCATGCCATGCTGCTCACCTCCCAGTCACAGCAGAATCCCTCAGCATTGCAATTATTATTATGATAACTTGTCTTTCTTCTTCACTAGATTTGGGAGAGACTTGAGGGCACTTGAGACTTGAGGTAATAGCATTTCTTTTATCTTTTTACTCCTGGCATCAATATGATGCCTGACATAGGGCAAACACTCAGGAAATATGGACAAATGAATGAGTGAATGGACTAGATCTCTTGTTGAC... |
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