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_41300 | A genetic alteration is present on Chromosome 11. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TGCAAGATGATTGAACTCAGAGGAGAGTACTGCTGCCCAGTGCACCCCACAAACTGTTCCTTTAATCTTCTTTGGAGCCTGGCCCCTTAAGCACCGACTGTGCTAAGCGATTATACGCTTTCAGGGGAGGGGAAAATGCCCAAGAGGTGAGATAGGATCTTTATTTCTACTTACTCCCTGGAGACACTGGGATGGCAACAAGGGTAGGAGACAAGGGCACCTGGATTAAAGCCCTGTGGGCCAAGAGTTGTGATAACCAACTTGGAATTTCCTGACTCCTATGCTTACTGATTTTTCCCAACCTGGTATGTTTGTATGTT... | TGCAAGATGATTGAACTCAGAGGAGAGTACTGCTGCCCAGTGCACCCCACAAACTGTTCCTTTAATCTTCTTTGGAGCCTGGCCCCTTAAGCACCGACTGTGCTAAGCGATTATACGCTTTCAGGGGAGGGGAAAATGCCCAAGAGGTGAGATAGGATCTTTATTTCTACTTACTCCCTGGAGACACTGGGATGGCAACAAGGGTAGGAGACAAGGGCACCTGGATTAAAGCCCTGTGGGCCAAGAGTTGTGATAACCAACTTGGAATTTCCTGACTCCTATGCTTACTGATTTTTCCCAACCTGGTATGTTTGTATGTT... |
Task1_train_41301 | A variant was discovered on Chromosome 11. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | AAGTATTAGAAACAGTTAATGAATAAACAAAGTGCTGAGGGAGAGAAGAGGAGGACATGATTTACTTAGCCCAGGGAAGAACGGTAGGATATTTACTAGCTGCCACCCAGAGAAAAGATCTAAGCAAAACAAGTAACAAAGCCGGGCCCCTAGGCTGATGCCTATAATCCCAACACTTTGGGGAAGTCAAGGCAAGAGGATTGCTTGAGGCCAGGATTCCAAACCAGCTGGGGCAACACAGAGAGACCCCATCTCTACAAAAATTAAAAAGTATTTAAAAATTATTAAAAAGTTAAAAAACATTAAAAATATACTGCACA... | AAGTATTAGAAACAGTTAATGAATAAACAAAGTGCTGAGGGAGAGAAGAGGAGGACATGATTTACTTAGCCCAGGGAAGAACGGTAGGATATTTACTAGCTGCCACCCAGAGAAAAGATCTAAGCAAAACAAGTAACAAAGCCGGGCCCCTAGGCTGATGCCTATAATCCCAACACTTTGGGGAAGTCAAGGCAAGAGGATTGCTTGAGGCCAGGATTCCAAACCAGCTGGGGCAACACAGAGAGACCCCATCTCTACAAAAATTAAAAAGTATTTAAAAATTATTAAAAAGTTAAAAAACATTAAAAATATACTGCACA... |
Task1_train_41302 | Here is a variant on Chromosome 11. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TCCTGTCCCTGTCTCCTACAGACCTCTTCTTGGGTGAATTTGGTATTGTGGTGTGTGGTCTTGGTGCTCCAGGTCGTGCAGTGGAAGTCTGAAGCCACCCCATACCGGCCTCTGGAGAGGGGTGACCCTGAGTGGAGCTCTGAGACAGATGCTCTCGTTGGGTCACGCCTTTCCCATTCCTGAAGAATAAGCGGAGTGCTTCCTGCAGCCGAAGACTCCATGCCCAAGTGCCTGTAATCCCCCCCCTCAAGGCCCTGTTTATGTTGGGAGTCTTAGTTTTCCTTTCGTTGGGGGGTGGGGGGGAAACATAATGACAGGCC... | TCCTGTCCCTGTCTCCTACAGACCTCTTCTTGGGTGAATTTGGTATTGTGGTGTGTGGTCTTGGTGCTCCAGGTCGTGCAGTGGAAGTCTGAAGCCACCCCATACCGGCCTCTGGAGAGGGGTGACCCTGAGTGGAGCTCTGAGACAGATGCTCTCGTTGGGTCACGCCTTTCCCATTCCTGAAGAATAAGCGGAGTGCTTCCTGCAGCCGAAGACTCCATGCCCAAGTGCCTGTAATCCCCCCCCTCAAGGCCCTGTTTATGTTGGGAGTCTTAGTTTTCCTTTCGTTGGGGGGTGGGGGGGAAACATAATGACAGGCC... |
Task1_train_41303 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | GTTATTATTATACTTTAAGTTTTAGGGTACATATGCACAATGTGCAGGTTTGTTACATATGTATACATGTGCCATGTTGGTGTGCTGCACTCATTAGCTTATCATTTAGCATTAGGTATATCTCCTAATGCTATCCCTCCCCCCTCCCCCGACCCCACAACAGTCCCCAGAGTGTGATGTTCCCCTTCCTGTGTCCATGTGTTCTCATTGTTCAATTCCCACCTATGAGTGAGAACATGCAGTGTTTGGTTTTTTGTCCTTGCGATAGTTTGCTGAGAATGATGGTTTCCAGTCCCTACAAAGGACATGGACTCATCATT... | GTTATTATTATACTTTAAGTTTTAGGGTACATATGCACAATGTGCAGGTTTGTTACATATGTATACATGTGCCATGTTGGTGTGCTGCACTCATTAGCTTATCATTTAGCATTAGGTATATCTCCTAATGCTATCCCTCCCCCCTCCCCCGACCCCACAACAGTCCCCAGAGTGTGATGTTCCCCTTCCTGTGTCCATGTGTTCTCATTGTTCAATTCCCACCTATGAGTGAGAACATGCAGTGTTTGGTTTTTTGTCCTTGCGATAGTTTGCTGAGAATGATGGTTTCCAGTCCCTACAAAGGACATGGACTCATCATT... |
Task1_train_41304 | This genomic variant is located on Chromosome 11. Can you determine its pathogenicity and name any linked disease? | Benign | GTCCCTGTACAAGGTTCCTGACCTGTGTTAAGTAAAGAATGTCACTTTCTAACAGGCCCAGGAACCCCAAGTTATCTTGAGGAGAGGACTTTGTTCAACTCATAGGTATCTGAGGGTTCAAACCCATGGCTGGGCTCGGCTTTTAAAAAGCCTTATCTGAGATTCTTCATGGAACAGAGTTTCATCAAAGCCAATTAAAAAAGCCTAAGTGAAAAATAATTATTCTTGCTGCACTTTATGCAAATAATCAGGCCAAGTACAGTGAAACTAAAGTTTGTTTTGTAAACTGTAAGTCAGTTCTATCATAATTTGTTTTTAAT... | GTCCCTGTACAAGGTTCCTGACCTGTGTTAAGTAAAGAATGTCACTTTCTAACAGGCCCAGGAACCCCAAGTTATCTTGAGGAGAGGACTTTGTTCAACTCATAGGTATCTGAGGGTTCAAACCCATGGCTGGGCTCGGCTTTTAAAAAGCCTTATCTGAGATTCTTCATGGAACAGAGTTTCATCAAAGCCAATTAAAAAAGCCTAAGTGAAAAATAATTATTCTTGCTGCACTTTATGCAAATAATCAGGCCAAGTACAGTGAAACTAAAGTTTGTTTTGTAAACTGTAAGTCAGTTCTATCATAATTTGTTTTTAAT... |
Task1_train_41305 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | TAACTGAGGTAAGATGAGATCTCATTGTAGTTTTGATTTGCATTTCTCTGAGGATCAATGATGTTCAGCACTTTTTCCTATGACTGTTTGACATCTGTATGTCTTCTTTTGAGAAATACCTATTCACGTTGCCCATTGTTTGATGAGATTATTTGATTTTTCCTATAGAGTTGTTTGAGCTCCTTATATATTCTGGTGATTAGTCCTTTGTCAGAGGGGTAGTTTGCAAGTATTTTCTCCCATTCTGTGGGTTGCCTCTTTACTTTGTTGAATGTATCCTTTGCTGTGCAGAAGTTTTTTAACTTGCTGTGATCCCATTT... | TAACTGAGGTAAGATGAGATCTCATTGTAGTTTTGATTTGCATTTCTCTGAGGATCAATGATGTTCAGCACTTTTTCCTATGACTGTTTGACATCTGTATGTCTTCTTTTGAGAAATACCTATTCACGTTGCCCATTGTTTGATGAGATTATTTGATTTTTCCTATAGAGTTGTTTGAGCTCCTTATATATTCTGGTGATTAGTCCTTTGTCAGAGGGGTAGTTTGCAAGTATTTTCTCCCATTCTGTGGGTTGCCTCTTTACTTTGTTGAATGTATCCTTTGCTGTGCAGAAGTTTTTTAACTTGCTGTGATCCCATTT... |
Task1_train_41306 | A mutation located on Chromosome 11 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | AGATTGCATTCAAGTCTGCTTTCTGGGCCACATCCTATATTTATCAGGTTAGGCTCTGCACCTCTGGGAAAACCTGTGACTGGTGAGTAAGCTTAATTCTGGGATGAAGTGTTAGAAATCCTGTTGAGGCAAGGTACGTGAAGTCATGTCTTCTATTCCAGTTTTCTCAGTAGTACAAATGCTAAAAATTTTGATCTCCATGTTTCTGAACCCTTTAACTATCTCTCAGTTATGTGTGGTTTGGGCATAGGAGATGAATGTTACGTACTGAACTCGCTGACCACTAAAATTAGACTGATCAACGGATTGCTATTGACATA... | AGATTGCATTCAAGTCTGCTTTCTGGGCCACATCCTATATTTATCAGGTTAGGCTCTGCACCTCTGGGAAAACCTGTGACTGGTGAGTAAGCTTAATTCTGGGATGAAGTGTTAGAAATCCTGTTGAGGCAAGGTACGTGAAGTCATGTCTTCTATTCCAGTTTTCTCAGTAGTACAAATGCTAAAAATTTTGATCTCCATGTTTCTGAACCCTTTAACTATCTCTCAGTTATGTGTGGTTTGGGCATAGGAGATGAATGTTACGTACTGAACTCGCTGACCACTAAAATTAGACTGATCAACGGATTGCTATTGACATA... |
Task1_train_41307 | A variant on Chromosome 11 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | CACATATTCTCACTCATAAGTGGGAGTTGAACAATGAGGACACATGGACACAGGGAGGGGAATATCACATCCTGGGGCCTGTTGTGGGATGGGAGACTAGGGGAGGGATAGCATTAGGAGAAATACCTAATGTCAATGGTGGGTTGATGGGTGTAGCAAACCACAATGGCACATGTATATCTGTGTAACAAACCTGCACGTTTTGCACATGTATTCCAGAACTTAGAGTATAATAAAATAAAAGTGGGCATAGGACATGGACAGACACTTTTCTTTTTTTAATTTATTTTAGATTTGGGGCACATGTGAACGTTTGTTAC... | CACATATTCTCACTCATAAGTGGGAGTTGAACAATGAGGACACATGGACACAGGGAGGGGAATATCACATCCTGGGGCCTGTTGTGGGATGGGAGACTAGGGGAGGGATAGCATTAGGAGAAATACCTAATGTCAATGGTGGGTTGATGGGTGTAGCAAACCACAATGGCACATGTATATCTGTGTAACAAACCTGCACGTTTTGCACATGTATTCCAGAACTTAGAGTATAATAAAATAAAAGTGGGCATAGGACATGGACAGACACTTTTCTTTTTTTAATTTATTTTAGATTTGGGGCACATGTGAACGTTTGTTAC... |
Task1_train_41308 | This sequence variant lies on Chromosome 11. Is it clinically significant, and what condition might it cause if any? | Benign | CCTGACGGTTTCTCTAGGAGATCAATTGATCACTTGCCCTTTGGTTAATCACACTTTTGATAACAAGCATGGCATGTCTAGGCCTTGCGATTATATCCCATTTGAGGACACGATATGATTGCTTCCTTTGTGTGGGCTCTGTCTAGGTTCTTCCTCATTACTATGTCTTCAGTGACCAGTCTACTCACTGCTATCCGTGTAGCCACACTTGGACGTGATGTTAAGTCACCATGAATGCAGCCCTTGATTAGGGGAAACCTTTTTGACTTTAACGAAGTAGAAATCCTTTGTTTACAAGCAGAGAAAGAATATATGATAGG... | CCTGACGGTTTCTCTAGGAGATCAATTGATCACTTGCCCTTTGGTTAATCACACTTTTGATAACAAGCATGGCATGTCTAGGCCTTGCGATTATATCCCATTTGAGGACACGATATGATTGCTTCCTTTGTGTGGGCTCTGTCTAGGTTCTTCCTCATTACTATGTCTTCAGTGACCAGTCTACTCACTGCTATCCGTGTAGCCACACTTGGACGTGATGTTAAGTCACCATGAATGCAGCCCTTGATTAGGGGAAACCTTTTTGACTTTAACGAAGTAGAAATCCTTTGTTTACAAGCAGAGAAAGAATATATGATAGG... |
Task1_train_41309 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TCTTAGATACACCACCAAAGGCACTATTCATAGAGATTTATATGAAATCATGTTGTATGTCCACTTCTTTGGCGGTCTCCTTCATATAACTATTTTGAGTGACATCCGTGTTGTTGCTTTTTATCAACAGTTCATTCCTTTTTATTACTGAGCAGTATTTCATTACATTTCCGTTTTATAAAAGGAAAAGCTGACACATTGGACTTCATCAAAATTTAAGAACCTGTTCTGAAGAGACAAGCCACAGATGGAGAGAAAATATTATAAAGTATATATCTGATGACGTACTTGTATACAGAACTTCTGAAGAACTCTCAAAA... | TCTTAGATACACCACCAAAGGCACTATTCATAGAGATTTATATGAAATCATGTTGTATGTCCACTTCTTTGGCGGTCTCCTTCATATAACTATTTTGAGTGACATCCGTGTTGTTGCTTTTTATCAACAGTTCATTCCTTTTTATTACTGAGCAGTATTTCATTACATTTCCGTTTTATAAAAGGAAAAGCTGACACATTGGACTTCATCAAAATTTAAGAACCTGTTCTGAAGAGACAAGCCACAGATGGAGAGAAAATATTATAAAGTATATATCTGATGACGTACTTGTATACAGAACTTCTGAAGAACTCTCAAAA... |
Task1_train_41310 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | TCCGATCTGCTATTATTTCCCTTTGCCATCCAAGAGACAGTTTGCTGCATTATCAGCTGATGCAGTAAGTGCCAGGGTAAGGTATTAGCCACAAAGTTATTTTGGGAAATATTTTTCTATGCCTTTTTCAGAGCATTGCAAAGGCCAGGAGTCATCCTCCCACCCCCTGGGGCTTTACCTGACCTTAAAAACTCAAGGGCAGATGTAGTACACAGCTTGTTCTAGAAGATTTCCACTGGTCAGATCGCCTTTCCCCTCAGTGGCAGCTTGGCTGACCACCTCCCGCTTCATGAGGCTGCATCTTTACAGGATCTGCTGAT... | TCCGATCTGCTATTATTTCCCTTTGCCATCCAAGAGACAGTTTGCTGCATTATCAGCTGATGCAGTAAGTGCCAGGGTAAGGTATTAGCCACAAAGTTATTTTGGGAAATATTTTTCTATGCCTTTTTCAGAGCATTGCAAAGGCCAGGAGTCATCCTCCCACCCCCTGGGGCTTTACCTGACCTTAAAAACTCAAGGGCAGATGTAGTACACAGCTTGTTCTAGAAGATTTCCACTGGTCAGATCGCCTTTCCCCTCAGTGGCAGCTTGGCTGACCACCTCCCGCTTCATGAGGCTGCATCTTTACAGGATCTGCTGAT... |
Task1_train_41311 | A genomic change on Chromosome 11 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TTAGCTGGGCTTGATGGTGCCTGCCTGTAATCCCAGCTACTTGAGAGGCTGAGGCAGGAGAATGGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCTGAGATTGCGCCATTGCACTTCAGCCTGGGCAACAAGAAAAAGACTCCGTATCAAAAAAAAAAAAAAAAGATTTTGGAGGGGGTCCACCTTTTTCAGTACCCTTTAGTTTAGAACATCACAGCTATTTATTTGTACATGGGACAGATTCTCCCTGTGGATAGAATAGAATAATTCTAGTCTCATTTTTCAGATTCAGGAAGGGCCCATTGCATCTCCTAAAAA... | TTAGCTGGGCTTGATGGTGCCTGCCTGTAATCCCAGCTACTTGAGAGGCTGAGGCAGGAGAATGGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCTGAGATTGCGCCATTGCACTTCAGCCTGGGCAACAAGAAAAAGACTCCGTATCAAAAAAAAAAAAAAAAGATTTTGGAGGGGGTCCACCTTTTTCAGTACCCTTTAGTTTAGAACATCACAGCTATTTATTTGTACATGGGACAGATTCTCCCTGTGGATAGAATAGAATAATTCTAGTCTCATTTTTCAGATTCAGGAAGGGCCCATTGCATCTCCTAAAAA... |
Task1_train_41312 | Located on Chromosome 11, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | AAAAAAATAAAGAAAAAAAAAGAAACATAATGTTTGTAAAGGTACTTTGCAAGCTTTATCTCTGTGTTGTCTTGAAATCTAAATTTCCAGAGAAAAAGATGAATGCTCTAAACCTGTCCATGGTAGAGGGAGGCTAGTTCTGTTCCAGGAGTCCAGCCTTATGAAGACAGTCTATTCTCTATTTTGTTCCTTCCTCTAGGGAGGTAAGATATGAGATCTTGCCTGTGTTCCACAGCGCTCAGCCATGAGATAATTAATAGCTGGTGTTGGTAGAGTTTGTGGCTATAAGAACAATCCCTGTGAGTTCCTGGTATCTGAAC... | AAAAAAATAAAGAAAAAAAAAGAAACATAATGTTTGTAAAGGTACTTTGCAAGCTTTATCTCTGTGTTGTCTTGAAATCTAAATTTCCAGAGAAAAAGATGAATGCTCTAAACCTGTCCATGGTAGAGGGAGGCTAGTTCTGTTCCAGGAGTCCAGCCTTATGAAGACAGTCTATTCTCTATTTTGTTCCTTCCTCTAGGGAGGTAAGATATGAGATCTTGCCTGTGTTCCACAGCGCTCAGCCATGAGATAATTAATAGCTGGTGTTGGTAGAGTTTGTGGCTATAAGAACAATCCCTGTGAGTTCCTGGTATCTGAAC... |
Task1_train_41313 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | AAACTCCTGGGCTCAAGCTATCTGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGCAAGCCACCGCCCCGGCCTGTCCTTTGTCCTTTTGGGTTTATCTTCCTAAACCTTTGCTATCAATTTTGGGTGAGTTTCAGCGGGATTGTTGGTCTTCTGTGGGTAACTGGGATCCCCTCTTGGAGTCTCTGCCTTCCCAGTTCCTTTTCTCTGGAATCCTCTTCCTTCACGCTTCCCTTGAGTGGCCCACTGTCATCCTTCCTATCTCTACTCAGCTTGTCACCTCCTCAGGGAAGCCTTCCCTGACTGCTTCCCCAT... | AAACTCCTGGGCTCAAGCTATCTGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGCAAGCCACCGCCCCGGCCTGTCCTTTGTCCTTTTGGGTTTATCTTCCTAAACCTTTGCTATCAATTTTGGGTGAGTTTCAGCGGGATTGTTGGTCTTCTGTGGGTAACTGGGATCCCCTCTTGGAGTCTCTGCCTTCCCAGTTCCTTTTCTCTGGAATCCTCTTCCTTCACGCTTCCCTTGAGTGGCCCACTGTCATCCTTCCTATCTCTACTCAGCTTGTCACCTCCTCAGGGAAGCCTTCCCTGACTGCTTCCCCAT... |
Task1_train_41314 | A variant on Chromosome 11 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | GGCGCAAGCCACCGCCCCGGCCTGTCCTTTGTCCTTTTGGGTTTATCTTCCTAAACCTTTGCTATCAATTTTGGGTGAGTTTCAGCGGGATTGTTGGTCTTCTGTGGGTAACTGGGATCCCCTCTTGGAGTCTCTGCCTTCCCAGTTCCTTTTCTCTGGAATCCTCTTCCTTCACGCTTCCCTTGAGTGGCCCACTGTCATCCTTCCTATCTCTACTCAGCTTGTCACCTCCTCAGGGAAGCCTTCCCTGACTGCTTCCCCATGTTCCATTCTGTCATCTCCATTGAACTTGGGGGGGCCTTAGACTGAGGGCTCATGTG... | GGCGCAAGCCACCGCCCCGGCCTGTCCTTTGTCCTTTTGGGTTTATCTTCCTAAACCTTTGCTATCAATTTTGGGTGAGTTTCAGCGGGATTGTTGGTCTTCTGTGGGTAACTGGGATCCCCTCTTGGAGTCTCTGCCTTCCCAGTTCCTTTTCTCTGGAATCCTCTTCCTTCACGCTTCCCTTGAGTGGCCCACTGTCATCCTTCCTATCTCTACTCAGCTTGTCACCTCCTCAGGGAAGCCTTCCCTGACTGCTTCCCCATGTTCCATTCTGTCATCTCCATTGAACTTGGGGGGGCCTTAGACTGAGGGCTCATGTG... |
Task1_train_41315 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | AAACCCTGTATCTACTAAAAATACAAAAATTAGCCGAGTGTGGTGGCAGGCGCCTATAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGTCTTGAACTCGGGAGGTGGAGGTTGCAGTGAGCCGAGATTGTGCCACTGCACTCCAGCCTGGGTGCGAACGAGTGAGACTCAGTCTCAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAAAGAGCCTGCGCGATGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATCATGAGGTCAGGAGTTCGAGACCAGCCTGACCAAC... | AAACCCTGTATCTACTAAAAATACAAAAATTAGCCGAGTGTGGTGGCAGGCGCCTATAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGTCTTGAACTCGGGAGGTGGAGGTTGCAGTGAGCCGAGATTGTGCCACTGCACTCCAGCCTGGGTGCGAACGAGTGAGACTCAGTCTCAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAAAGAGCCTGCGCGATGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATCATGAGGTCAGGAGTTCGAGACCAGCCTGACCAAC... |
Task1_train_41316 | A mutation found on Chromosome 11 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AAAAGAGCCTGCGCGATGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATCATGAGGTCAGGAGTTCGAGACCAGCCTGACCAACATGGTGAAACCCCGTCTCTACTAAAAACACAAAAATCAGCCACAAGTGGTGGCACGTACCTGTAATCCCATGTACTCGGGAGGCTGAGACAGGAGAATCACTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCGAGATCGAGCCACTGTACTCCAGCCTGGCAACAAAGCGACACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAGAGATTTCAGGTCAG... | AAAAGAGCCTGCGCGATGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATCATGAGGTCAGGAGTTCGAGACCAGCCTGACCAACATGGTGAAACCCCGTCTCTACTAAAAACACAAAAATCAGCCACAAGTGGTGGCACGTACCTGTAATCCCATGTACTCGGGAGGCTGAGACAGGAGAATCACTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCGAGATCGAGCCACTGTACTCCAGCCTGGCAACAAAGCGACACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAGAGATTTCAGGTCAG... |
Task1_train_41317 | A variant has been detected on Chromosome 11. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TCCCCCAGCACACAAGGAAGACCAGATGTAGCTACAGGATGATGAAACATGGTTTCAAACGAGTTCTTTCTTGTTACTTTTTAAAATTTCTTTTTTATAAATTAATATTTTATTGTTGGATCCTCCTCCTTTCTCTGGAGCTGTGCTTGGGGCTACTCTGACACTCTGTCTCTTCATCACCAGCCAAGGAAAGGGGCTTTCCTGATAAAGACAAGAGTTGGTTAGAGAAAGGGACACCTAAGTCAGTCTAGGGTTGGAAGCTAGGAGAGAGGTGAGGGCAGAAGGGCACAGCTTTCAGGAACAAGGAATAGGGGCTGGGG... | TCCCCCAGCACACAAGGAAGACCAGATGTAGCTACAGGATGATGAAACATGGTTTCAAACGAGTTCTTTCTTGTTACTTTTTAAAATTTCTTTTTTATAAATTAATATTTTATTGTTGGATCCTCCTCCTTTCTCTGGAGCTGTGCTTGGGGCTACTCTGACACTCTGTCTCTTCATCACCAGCCAAGGAAAGGGGCTTTCCTGATAAAGACAAGAGTTGGTTAGAGAAAGGGACACCTAAGTCAGTCTAGGGTTGGAAGCTAGGAGAGAGGTGAGGGCAGAAGGGCACAGCTTTCAGGAACAAGGAATAGGGGCTGGGG... |
Task1_train_41318 | A variant was discovered on Chromosome 11. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | TTAGGTACCTGGTTGAACGGGTAGCAGTGAGACCCCCTTCGCAGGCAGGGGTCCCTCCCATCTCGTCTCGCACTTGTCCCCTCACCCCGACCTGCAGGGAATGGCCCTGGTTGGCCCGGATGAGAAGGCCAGTGCTGGGATCCCCCAGCTGCAGGGCGAACCGCTGCTTCCTATTGGTGTCCACCACGCGCTGCACATCTTCAGCAGAGAAGCCGCGGAACTGGGGCAACTGCAGGAGGGTGCCCAGGGGCACGAAGCCATCTGTGGGCAGGCAGGGTGCTCAGGAGCTAACCTTGCTCTGGACTGGGCCAGGGTTAACA... | TTAGGTACCTGGTTGAACGGGTAGCAGTGAGACCCCCTTCGCAGGCAGGGGTCCCTCCCATCTCGTCTCGCACTTGTCCCCTCACCCCGACCTGCAGGGAATGGCCCTGGTTGGCCCGGATGAGAAGGCCAGTGCTGGGATCCCCCAGCTGCAGGGCGAACCGCTGCTTCCTATTGGTGTCCACCACGCGCTGCACATCTTCAGCAGAGAAGCCGCGGAACTGGGGCAACTGCAGGAGGGTGCCCAGGGGCACGAAGCCATCTGTGGGCAGGCAGGGTGCTCAGGAGCTAACCTTGCTCTGGACTGGGCCAGGGTTAACA... |
Task1_train_41319 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | ACTCAGCTGTCTCCCTAACCTTCAACCTAGGTTTAGCTGCCTCTCAACTGCAGGTTCATTACTTCAGTTGACAGATGTTTGGTGGCTGCTGGGGCGCCTGAAAATAAGTCTGGTGGGGGAACAGGCCCAGCCAGATCATTCCAGTCATGAGTCACAGCCCAGGTGCACAGGTAGAGGTAAGCCTGGCTCCTGGGAGAGAGATGTGGGCAGGAGCATTGGCTGGAAGCCAGGGCTTGTCATTGGACATCATCTCGGTCCTGCAGGGGCCCTGTGGGGTGGGTGTCATCAAGCCCGTGTTACACGCCTGTATTGGATGACAA... | ACTCAGCTGTCTCCCTAACCTTCAACCTAGGTTTAGCTGCCTCTCAACTGCAGGTTCATTACTTCAGTTGACAGATGTTTGGTGGCTGCTGGGGCGCCTGAAAATAAGTCTGGTGGGGGAACAGGCCCAGCCAGATCATTCCAGTCATGAGTCACAGCCCAGGTGCACAGGTAGAGGTAAGCCTGGCTCCTGGGAGAGAGATGTGGGCAGGAGCATTGGCTGGAAGCCAGGGCTTGTCATTGGACATCATCTCGGTCCTGCAGGGGCCCTGTGGGGTGGGTGTCATCAAGCCCGTGTTACACGCCTGTATTGGATGACAA... |
Task1_train_41320 | A variant on Chromosome 11 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | CTCAGCCTCCCAAGTAGCTGGGATTACAGGCATTCGCCACCACGCCCGGCTAATTTTGTATTTTTAGTAGAGATGGGGTTTCTCCATGTTGGTCAGGCTGGTCTCAAACTCTCAACCTCAGGTGATCCGCCTGCCTCGCCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCTCGCCCAGCCTGCAGGGTGCTTTTAAGAGGCTGGAAGGGGGTTGGGTGCGGTGACTCATGCCTGTAATCCCAGAACTTTGGGAGGCTGAAGCAGGCAGATTACTTGAGCCCACGTTTTGAGACCAGTCTGGGCAACATAGCATGA... | CTCAGCCTCCCAAGTAGCTGGGATTACAGGCATTCGCCACCACGCCCGGCTAATTTTGTATTTTTAGTAGAGATGGGGTTTCTCCATGTTGGTCAGGCTGGTCTCAAACTCTCAACCTCAGGTGATCCGCCTGCCTCGCCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCTCGCCCAGCCTGCAGGGTGCTTTTAAGAGGCTGGAAGGGGGTTGGGTGCGGTGACTCATGCCTGTAATCCCAGAACTTTGGGAGGCTGAAGCAGGCAGATTACTTGAGCCCACGTTTTGAGACCAGTCTGGGCAACATAGCATGA... |
Task1_train_41321 | A mutation located on Chromosome 11 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | TTGGACCTGGGCCGCGCAGCCCAGGCCCGCGAGCCGCCGCGACCCCTTCCGTCTCTGTCGCTGGATGTCAGGCAGAGCCTAAGTTTCCCTCGTAAGACAGCGGCCTCTTTTGAAAGTATCCGTGAGAGCACTACCCCGGCCTGCCGGAGCCCCAGTCGACGCACAGAAAAGCCTCGGCGGCACAGACGCGGGCTTTATTAACATTTGGTAGTGAGCACGGCCCCCAGGGCATCGCGGGGGCTCGGGTCCCGGTGACGCAACGGTTAAACCTGGCTCGCGACTTAGCGCAGGCGCCTGGGGGAAAGCCCGGAGCCTGAGGG... | TTGGACCTGGGCCGCGCAGCCCAGGCCCGCGAGCCGCCGCGACCCCTTCCGTCTCTGTCGCTGGATGTCAGGCAGAGCCTAAGTTTCCCTCGTAAGACAGCGGCCTCTTTTGAAAGTATCCGTGAGAGCACTACCCCGGCCTGCCGGAGCCCCAGTCGACGCACAGAAAAGCCTCGGCGGCACAGACGCGGGCTTTATTAACATTTGGTAGTGAGCACGGCCCCCAGGGCATCGCGGGGGCTCGGGTCCCGGTGACGCAACGGTTAAACCTGGCTCGCGACTTAGCGCAGGCGCCTGGGGGAAAGCCCGGAGCCTGAGGG... |
Task1_train_41322 | A variant on Chromosome 11 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | CCCTGGCACATGAGCGCGCCCCCAAAGACCATAAGCCTCTCCCACAGGCTCCTGGGGGCGGGAGTGGGGAGTATGGGAGTGGGGATTGTTGGTGTCTCCTGGGTCCTGCCTACTGCCCCATCCCGCAGAAGTGGCACGTGCCACCGGAGCTAGTAAGAGTGCTGTCGGCGATGCTTTTCCTGCTGATCGGCTGCCTGCTCTTTGTCCTCACGCCCACGTTCGTGTTCTGCTATATGGAGGACTGGAGCAAGCTGGAGGCCATCTACTTTGTCATAGTGACGCTTACCACCGTGGGCTTTGGCGACTATGTGGCCGGTGAG... | CCCTGGCACATGAGCGCGCCCCCAAAGACCATAAGCCTCTCCCACAGGCTCCTGGGGGCGGGAGTGGGGAGTATGGGAGTGGGGATTGTTGGTGTCTCCTGGGTCCTGCCTACTGCCCCATCCCGCAGAAGTGGCACGTGCCACCGGAGCTAGTAAGAGTGCTGTCGGCGATGCTTTTCCTGCTGATCGGCTGCCTGCTCTTTGTCCTCACGCCCACGTTCGTGTTCTGCTATATGGAGGACTGGAGCAAGCTGGAGGCCATCTACTTTGTCATAGTGACGCTTACCACCGTGGGCTTTGGCGACTATGTGGCCGGTGAG... |
Task1_train_41323 | Assess the clinical impact of this variant found on Chromosome 11. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | CCACCGGAGCTAGTAAGAGTGCTGTCGGCGATGCTTTTCCTGCTGATCGGCTGCCTGCTCTTTGTCCTCACGCCCACGTTCGTGTTCTGCTATATGGAGGACTGGAGCAAGCTGGAGGCCATCTACTTTGTCATAGTGACGCTTACCACCGTGGGCTTTGGCGACTATGTGGCCGGTGAGGCCGCCCTTCTTGTGCTGCACTTTCCCATCTACTTTATTCCTGATCAGGGGCTCTGCACTCCTGCCTTTCCCTCCAGATCCCATGTGGTTGCTCTAACCCCTGCATCCATCATGGAATGCACCATCACAGCCTTGCACAC... | CCACCGGAGCTAGTAAGAGTGCTGTCGGCGATGCTTTTCCTGCTGATCGGCTGCCTGCTCTTTGTCCTCACGCCCACGTTCGTGTTCTGCTATATGGAGGACTGGAGCAAGCTGGAGGCCATCTACTTTGTCATAGTGACGCTTACCACCGTGGGCTTTGGCGACTATGTGGCCGGTGAGGCCGCCCTTCTTGTGCTGCACTTTCCCATCTACTTTATTCCTGATCAGGGGCTCTGCACTCCTGCCTTTCCCTCCAGATCCCATGTGGTTGCTCTAACCCCTGCATCCATCATGGAATGCACCATCACAGCCTTGCACAC... |
Task1_train_41324 | A genomic change on Chromosome 11 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CCGAGCATTTTGGGAGGCTGAGGCGGGTGGATCACGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACACAGTGAAACCCCGTCTCTACTAAAAATACAAAAATTACCTGGACGTGGTGGCGGGCGCCTGTAATCCAAGCTACTTGGAGGGCTGAGGCAGGAGAATCGCTTGAACCGGGGAGGCAGAGGTTGCAGTGAGCTGAAATCACACCACTGCACCCCAGCCGGGATGACAGAGCTAGACTTGTCTCAAAAAAAGAAGAAAAAAAAAAAAAAAAAAAAAAAGCATGTCCCAAATATTGCACGAGATATATTTATACT... | CCGAGCATTTTGGGAGGCTGAGGCGGGTGGATCACGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACACAGTGAAACCCCGTCTCTACTAAAAATACAAAAATTACCTGGACGTGGTGGCGGGCGCCTGTAATCCAAGCTACTTGGAGGGCTGAGGCAGGAGAATCGCTTGAACCGGGGAGGCAGAGGTTGCAGTGAGCTGAAATCACACCACTGCACCCCAGCCGGGATGACAGAGCTAGACTTGTCTCAAAAAAAGAAGAAAAAAAAAAAAAAAAAAAAAAAGCATGTCCCAAATATTGCACGAGATATATTTATACT... |
Task1_train_41325 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | CATGCGTACTCCAGGATGCCTTCCCTGATCATCCTGCCGAGGTCAAATCCCCTCCCCTTCATAGCACCTAGTATGGCTACAACAGTCTCGAGTGTATAGAGGATGGGGTGGGGTGAGGTCACAGGAATGATGCTCCCTTCTATCTGGGGTTCAAGGGAGGCTTCTTGGAGGAGCATCTGAACCAGGCTTCCCAGGGGATGTGGTTTGGGTAACTTTGAGAAATACTGAAGGGAAAAGAAAGAACGCTGTAGTGAGTGAAGCCTGGCATTTGGGAAGATGGGTGTGTGGGTGACCAAACTCACCACGCAAGGCCCAGAGCC... | CATGCGTACTCCAGGATGCCTTCCCTGATCATCCTGCCGAGGTCAAATCCCCTCCCCTTCATAGCACCTAGTATGGCTACAACAGTCTCGAGTGTATAGAGGATGGGGTGGGGTGAGGTCACAGGAATGATGCTCCCTTCTATCTGGGGTTCAAGGGAGGCTTCTTGGAGGAGCATCTGAACCAGGCTTCCCAGGGGATGTGGTTTGGGTAACTTTGAGAAATACTGAAGGGAAAAGAAAGAACGCTGTAGTGAGTGAAGCCTGGCATTTGGGAAGATGGGTGTGTGGGTGACCAAACTCACCACGCAAGGCCCAGAGCC... |
Task1_train_41326 | The following genetic variant occurs on Chromosome 11. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | TTCACCATGTTGGCCAGGATGGTCTCAATCTCTTGACCTTGTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCACCTGGCCAACACACTTTTACTTATTCATTTAAACATGTTTACAGGCATCTTCTTGGTGCCAGGCCCTGTACCAGGCTCTGGGCACACAGCAGTGACCACGAAGCTAGCAATCCAGTGTTTGGGCGTGGCTTCAGCTTCCTTCCAAGCTAAGGAAGGGGTTAGGGCTTTTGCCATGGGGGATTGGGCAGCCACTGAAGGCTCCCCAATGGGCAAAGTGAGCAAA... | TTCACCATGTTGGCCAGGATGGTCTCAATCTCTTGACCTTGTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCACCTGGCCAACACACTTTTACTTATTCATTTAAACATGTTTACAGGCATCTTCTTGGTGCCAGGCCCTGTACCAGGCTCTGGGCACACAGCAGTGACCACGAAGCTAGCAATCCAGTGTTTGGGCGTGGCTTCAGCTTCCTTCCAAGCTAAGGAAGGGGTTAGGGCTTTTGCCATGGGGGATTGGGCAGCCACTGAAGGCTCCCCAATGGGCAAAGTGAGCAAA... |
Task1_train_41327 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | TGGCCCTCTCCGTGCATGAGCCTCAGCCCCCACTTCCCTTCTCTGACCTCCTTCCTGCAGGAGCCTCAGCACCCCCTCCCCTTGTCTGACCCCCTCCCTGCGTGAGCCTCAGCCTCCCCCCATTCTCTGACCTCCTCCCTACAGGAGCCTCAGCTCCCGTCCCCTCCTCTCACCCCCTCCCTGCATGTACCTCTTGCAGGGTCCCCTTCCCCGGCACCCATGCGCCGGGCCCAGAGCTCCCTCTGCCTGCGGGATGAGACCTTGGCAGGCGGGCAGCGGCGGAAACTCAGCTCAAGGTTCCCGGTGGGGCGAAGCTCTGA... | TGGCCCTCTCCGTGCATGAGCCTCAGCCCCCACTTCCCTTCTCTGACCTCCTTCCTGCAGGAGCCTCAGCACCCCCTCCCCTTGTCTGACCCCCTCCCTGCGTGAGCCTCAGCCTCCCCCCATTCTCTGACCTCCTCCCTACAGGAGCCTCAGCTCCCGTCCCCTCCTCTCACCCCCTCCCTGCATGTACCTCTTGCAGGGTCCCCTTCCCCGGCACCCATGCGCCGGGCCCAGAGCTCCCTCTGCCTGCGGGATGAGACCTTGGCAGGCGGGCAGCGGCGGAAACTCAGCTCAAGGTTCCCGGTGGGGCGAAGCTCTGA... |
Task1_train_41328 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | CTCAGCCTCCCCCCATTCTCTGACCTCCTCCCTACAGGAGCCTCAGCTCCCGTCCCCTCCTCTCACCCCCTCCCTGCATGTACCTCTTGCAGGGTCCCCTTCCCCGGCACCCATGCGCCGGGCCCAGAGCTCCCTCTGCCTGCGGGATGAGACCTTGGCAGGCGGGCAGCGGCGGAAACTCAGCTCAAGGTTCCCGGTGGGGCGAAGCTCTGAGTCATTCAGCCCTGGGGACACCCCTAGGCAACGATTCCGACAGCGCCATCCAGGCCCCCTGGGGGCGCCCGTCTCCCACAGCAAAGGTGAGGGACAAGGGTCACTGT... | CTCAGCCTCCCCCCATTCTCTGACCTCCTCCCTACAGGAGCCTCAGCTCCCGTCCCCTCCTCTCACCCCCTCCCTGCATGTACCTCTTGCAGGGTCCCCTTCCCCGGCACCCATGCGCCGGGCCCAGAGCTCCCTCTGCCTGCGGGATGAGACCTTGGCAGGCGGGCAGCGGCGGAAACTCAGCTCAAGGTTCCCGGTGGGGCGAAGCTCTGAGTCATTCAGCCCTGGGGACACCCCTAGGCAACGATTCCGACAGCGCCATCCAGGCCCCCTGGGGGCGCCCGTCTCCCACAGCAAAGGTGAGGGACAAGGGTCACTGT... |
Task1_train_41329 | A mutation on Chromosome 11 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GTACCAGCCAGCCCCCCAACTCTTTGTGGACCCACCAGCTCCTTGGGGGAGGAGGCTTCCTTCTTGTCCCCTGTGTCTCCTGCAAGCTCTGTCCACTTCCGCACTGGCCCTGGGCCCAGTGGTTGCCTTGTGCCTCCCAGGACCTGGTGTGGGATGGGAGAACTCCGCTGAGACCCTGCAGGAACACGAAACAGATGCCAACCGAGAGGGTGAGTGGGGGACTGTGGAAGGAGTAGTATTCTTTGTCCTGCCTGGGGCCCCTGGCAGAACCTCATTCATCCATTCTTTCATTCGACAATGATCCTTTACCAAGTGCCAGG... | GTACCAGCCAGCCCCCCAACTCTTTGTGGACCCACCAGCTCCTTGGGGGAGGAGGCTTCCTTCTTGTCCCCTGTGTCTCCTGCAAGCTCTGTCCACTTCCGCACTGGCCCTGGGCCCAGTGGTTGCCTTGTGCCTCCCAGGACCTGGTGTGGGATGGGAGAACTCCGCTGAGACCCTGCAGGAACACGAAACAGATGCCAACCGAGAGGGTGAGTGGGGGACTGTGGAAGGAGTAGTATTCTTTGTCCTGCCTGGGGCCCCTGGCAGAACCTCATTCATCCATTCTTTCATTCGACAATGATCCTTTACCAAGTGCCAGG... |
Task1_train_41330 | A mutation on Chromosome 11 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | GGTGGGAGGGGGCTTGCCGCCGTGGGTGGGTGTTGACCTTGGCCCGCCACGCCGCCCGCAGCTGCACACGTACCTGGTCCTGGAGCTGCTGCGGGGCGGGGAGCTGCTGGAGCACATCCGCAAGAAGCGGCACTTCAGCGAGTCGGAAGCAAGCCAGATCCTGCGCAGCCTCGTGTCGGCCGTGAGCTTCATGCACGAGGAGGCGGGCGTGGTGCACCGCGACCTCAAGCCGGAGGTGGGCGAGCTGCCTCGGCGGCGGGGCGGAGCGGTGGCGCCGGGGGCTGCCTCTGACCACTACCCCGCCGCCCTCGCAGAACATC... | GGTGGGAGGGGGCTTGCCGCCGTGGGTGGGTGTTGACCTTGGCCCGCCACGCCGCCCGCAGCTGCACACGTACCTGGTCCTGGAGCTGCTGCGGGGCGGGGAGCTGCTGGAGCACATCCGCAAGAAGCGGCACTTCAGCGAGTCGGAAGCAAGCCAGATCCTGCGCAGCCTCGTGTCGGCCGTGAGCTTCATGCACGAGGAGGCGGGCGTGGTGCACCGCGACCTCAAGCCGGAGGTGGGCGAGCTGCCTCGGCGGCGGGGCGGAGCGGTGGCGCCGGGGGCTGCCTCTGACCACTACCCCGCCGCCCTCGCAGAACATC... |
Task1_train_41331 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | CCGATGGGGGAGCCCCTCCCCACGCCCAGCCAGACCCTAATGGAAGAGGCTCCTCCCAGTGCTTCCTCTCCTCAGCGCCCCCTGCCCCCCGACACCACAGCCCCGCCCCGGGCCGCTCAGCCCAGGACCCGCCCGCACTTCACCACTTCACGGTCTTGGCCAGACTCTCGGCCTCCGGGCAGCGCGGGTGCTGGCCGGACCCCTCCCTCCGGTGAGCCTCTCTCCCAAGCGCCATTCCATAGTCAGCCCCACGGCCCAGGGTCCCACCTCGCCCTGTCCAGCCCAGCAATCTCCCATCAAACCCCACGCTCTCAGGGGTT... | CCGATGGGGGAGCCCCTCCCCACGCCCAGCCAGACCCTAATGGAAGAGGCTCCTCCCAGTGCTTCCTCTCCTCAGCGCCCCCTGCCCCCCGACACCACAGCCCCGCCCCGGGCCGCTCAGCCCAGGACCCGCCCGCACTTCACCACTTCACGGTCTTGGCCAGACTCTCGGCCTCCGGGCAGCGCGGGTGCTGGCCGGACCCCTCCCTCCGGTGAGCCTCTCTCCCAAGCGCCATTCCATAGTCAGCCCCACGGCCCAGGGTCCCACCTCGCCCTGTCCAGCCCAGCAATCTCCCATCAAACCCCACGCTCTCAGGGGTT... |
Task1_train_41332 | Assess the clinical impact of this variant found on Chromosome 11. State whether it’s pathogenic or benign, and the disease if applicable. | Benign | AGCCTGAAGCCAGAGAGAAGGGAGAAAGGGGAGGGGCTAGAGCCCCAGGGGAAAGACTCACCTGACCAGGTGGCACGTTTTCACCTGCAGGGAATTGGAGTTGTCCTTCCGGGATTGTTGGTAGGTGAAGGAGAGGGTTAAGGAGGCCGCTTAACTCTAGAAAGGGAGGCCTGCGTGGAGGGAGGCTGGGGGCGGGGCCTGGTTCTAGGAGACACGTTCTAGGGATGGGGCTTGCGCTCTGCGGAGATGCTGGGGGTGAGGCTTGAGCTCTGGGAGGGGTTGGAGGTGGGGGTGGAGGACTAGGTGCTGAGGGAGGCTGA... | AGCCTGAAGCCAGAGAGAAGGGAGAAAGGGGAGGGGCTAGAGCCCCAGGGGAAAGACTCACCTGACCAGGTGGCACGTTTTCACCTGCAGGGAATTGGAGTTGTCCTTCCGGGATTGTTGGTAGGTGAAGGAGAGGGTTAAGGAGGCCGCTTAACTCTAGAAAGGGAGGCCTGCGTGGAGGGAGGCTGGGGGCGGGGCCTGGTTCTAGGAGACACGTTCTAGGGATGGGGCTTGCGCTCTGCGGAGATGCTGGGGGTGAGGCTTGAGCTCTGGGAGGGGTTGGAGGTGGGGGTGGAGGACTAGGTGCTGAGGGAGGCTGA... |
Task1_train_41333 | Consider this mutation on Chromosome 11. Is this a benign change or a disease-causing variant? | Benign | CTGGGGTGGGCACAAAGCAGGTCACATGGGGGCTGCCTGGGGCCAGGAGGATAAGGCAGCCTCACCTGAGGTAGCTGCCAATGTAGGCCACCACATTGGGGTGGCGGCACTCACGCAGGATGGTGATTTCCTGCTGGAGGGAGCTGATGTCGTCCCCTGGGAAGCACAAAGCATCATGGGGAAGGCGCGCTGGGGTTGCCCTGACTCAGTGCCCCCATCTGCAAAATGGGCACAGAGTGCCTCCCTCCGGGCCAGGCAGGTGCAGGTGACAGCACCTCCCGGGGCACGCCTCTCAGGGGTCTCGGAAACGTCAACCCTCC... | CTGGGGTGGGCACAAAGCAGGTCACATGGGGGCTGCCTGGGGCCAGGAGGATAAGGCAGCCTCACCTGAGGTAGCTGCCAATGTAGGCCACCACATTGGGGTGGCGGCACTCACGCAGGATGGTGATTTCCTGCTGGAGGGAGCTGATGTCGTCCCCTGGGAAGCACAAAGCATCATGGGGAAGGCGCGCTGGGGTTGCCCTGACTCAGTGCCCCCATCTGCAAAATGGGCACAGAGTGCCTCCCTCCGGGCCAGGCAGGTGCAGGTGACAGCACCTCCCGGGGCACGCCTCTCAGGGGTCTCGGAAACGTCAACCCTCC... |
Task1_train_41334 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | ACATGCTTTTCCTGCCTTAATTTTCTAACAACTCTGAGCAAGTACTACTGTTATAATCCCTAATTTCCAGATGAGGGAATGGAACCCCTGGAGCCATGTGATGGTCAAGGTCAGGTCACTCAGCTGGTCCTGAGAGCTGCGATTTGGCCCTGGGCAGCTTGGGTGATATGCGGCACCCAACCTGCAGGCCCCACCCCAAAGAGCCATTGCTCACGAAGGACACTCTGCCCCTCTCTTCCAGCCCTTACCCATCATGCTAGTTACTTGTGCATGCACCAGACTGCCCCACTGCCTCATTCATTCATTCATTCACTCTTCCA... | ACATGCTTTTCCTGCCTTAATTTTCTAACAACTCTGAGCAAGTACTACTGTTATAATCCCTAATTTCCAGATGAGGGAATGGAACCCCTGGAGCCATGTGATGGTCAAGGTCAGGTCACTCAGCTGGTCCTGAGAGCTGCGATTTGGCCCTGGGCAGCTTGGGTGATATGCGGCACCCAACCTGCAGGCCCCACCCCAAAGAGCCATTGCTCACGAAGGACACTCTGCCCCTCTCTTCCAGCCCTTACCCATCATGCTAGTTACTTGTGCATGCACCAGACTGCCCCACTGCCTCATTCATTCATTCATTCACTCTTCCA... |
Task1_train_41335 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | CCCACCTCCCCTGGAGCCCTGCCCTCTGTCCTGTTGGGGTCTGAGCTTGCAGGTTCCAGAATGCACCATGCACCTGCACTCACCCCTTAGCCGCCTAGGACCATCGATCCCCTACAGAATTCATCTGACAACTGCCCACGAGACTGGCTCCCCAGCTTCCCTGGGGTCCTTCTGGCCTAGCGAAGCGTATGGCCTGAATGAACCAGGGCAGCCTCTGCGCCTCAGATTCTTAGTCTGCAAACACAGCCGTCCTCCACCCCCCTTTACAAGACATGCCATGAGCAGGAGACACAGTGGGCTCTGAAGGCCTGGGGGGCACT... | CCCACCTCCCCTGGAGCCCTGCCCTCTGTCCTGTTGGGGTCTGAGCTTGCAGGTTCCAGAATGCACCATGCACCTGCACTCACCCCTTAGCCGCCTAGGACCATCGATCCCCTACAGAATTCATCTGACAACTGCCCACGAGACTGGCTCCCCAGCTTCCCTGGGGTCCTTCTGGCCTAGCGAAGCGTATGGCCTGAATGAACCAGGGCAGCCTCTGCGCCTCAGATTCTTAGTCTGCAAACACAGCCGTCCTCCACCCCCCTTTACAAGACATGCCATGAGCAGGAGACACAGTGGGCTCTGAAGGCCTGGGGGGCACT... |
Task1_train_41336 | Given this variant on Chromosome 11, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CCAGGGGTCCGGCTCAGGCCGCAGGTCGGCAATGGGGAAGCGCAGCCGCAGCGTGGCCCGGGGTGCAGAGAGCCGAAATACCGTCTGCTGCTCCATCGCCGGCAGGGGCTCTGTCTGCAGGAGGATTGGGGGTCAGAGCAGCCGTCGGAGCCCCTCCCACTGTGACCAAGAGCCGAAGGACCCAGGCCCTGCACCCACCCCCGGCCTGGCCCTGGCAGGGGCCTCTCACCAGCAGGCCGGCTGGAGGCTCAGCAGGTACGGTGGCCAGGCGCAGTAGGGCGGCCAGCCGGTCCAGGGCCCCCAGCTCCACGTCCGCCTGG... | CCAGGGGTCCGGCTCAGGCCGCAGGTCGGCAATGGGGAAGCGCAGCCGCAGCGTGGCCCGGGGTGCAGAGAGCCGAAATACCGTCTGCTGCTCCATCGCCGGCAGGGGCTCTGTCTGCAGGAGGATTGGGGGTCAGAGCAGCCGTCGGAGCCCCTCCCACTGTGACCAAGAGCCGAAGGACCCAGGCCCTGCACCCACCCCCGGCCTGGCCCTGGCAGGGGCCTCTCACCAGCAGGCCGGCTGGAGGCTCAGCAGGTACGGTGGCCAGGCGCAGTAGGGCGGCCAGCCGGTCCAGGGCCCCCAGCTCCACGTCCGCCTGG... |
Task1_train_41337 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | ATGGGGAAGCGCAGCCGCAGCGTGGCCCGGGGTGCAGAGAGCCGAAATACCGTCTGCTGCTCCATCGCCGGCAGGGGCTCTGTCTGCAGGAGGATTGGGGGTCAGAGCAGCCGTCGGAGCCCCTCCCACTGTGACCAAGAGCCGAAGGACCCAGGCCCTGCACCCACCCCCGGCCTGGCCCTGGCAGGGGCCTCTCACCAGCAGGCCGGCTGGAGGCTCAGCAGGTACGGTGGCCAGGCGCAGTAGGGCGGCCAGCCGGTCCAGGGCCCCCAGCTCCACGTCCGCCTGGAAGTTGGCCAGGTCCAGGGCCAGTTCTGAGT... | ATGGGGAAGCGCAGCCGCAGCGTGGCCCGGGGTGCAGAGAGCCGAAATACCGTCTGCTGCTCCATCGCCGGCAGGGGCTCTGTCTGCAGGAGGATTGGGGGTCAGAGCAGCCGTCGGAGCCCCTCCCACTGTGACCAAGAGCCGAAGGACCCAGGCCCTGCACCCACCCCCGGCCTGGCCCTGGCAGGGGCCTCTCACCAGCAGGCCGGCTGGAGGCTCAGCAGGTACGGTGGCCAGGCGCAGTAGGGCGGCCAGCCGGTCCAGGGCCCCCAGCTCCACGTCCGCCTGGAAGTTGGCCAGGTCCAGGGCCAGTTCTGAGT... |
Task1_train_41338 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | TGACCCACCGTACCTGGCCTATAATTTTTTTTTTTTTTTTGAGATGGAGTCTCACTGTGTTGCCAGGCTGGAGTGCAGTGGCATGATCTCAGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCACTTGCCACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGATTTCACCATGTTGGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAAGTGATTCTCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGACACCACACC... | TGACCCACCGTACCTGGCCTATAATTTTTTTTTTTTTTTTGAGATGGAGTCTCACTGTGTTGCCAGGCTGGAGTGCAGTGGCATGATCTCAGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCACTTGCCACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGATTTCACCATGTTGGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAAGTGATTCTCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGACACCACACC... |
Task1_train_41339 | A mutation located on Chromosome 11 is being studied. Determine whether it’s pathogenic or benign, and specify the linked disease. | Benign | CACAGCAAACTCCTTAACTCGAGTGTGCAGGTGTCCCAGGTACTCTTCTGCTCTCTGCTCCCTGAGCAATACATGGAGGGCTGTAGGCCCAGCCAGGAGGTGCCTTCTCCCTCCTGCAGGAGGCCCGGACTTCTCAGGGCTCTCATGGAACTCACAGGGATGGGGTTAGAGAGGCACCCACTTTTTCCCTCTCCAGGATGATAGGGTATCATGATGCTTCCTGCCCCCGCACCTTCCCCTCAGAGGCCTTTTCACCAAAGGTGCACCAGATTTCCAGTCGCCTCGTGTGTAAGCTGCAGGTAGGATGTCCGACCCCCTTT... | CACAGCAAACTCCTTAACTCGAGTGTGCAGGTGTCCCAGGTACTCTTCTGCTCTCTGCTCCCTGAGCAATACATGGAGGGCTGTAGGCCCAGCCAGGAGGTGCCTTCTCCCTCCTGCAGGAGGCCCGGACTTCTCAGGGCTCTCATGGAACTCACAGGGATGGGGTTAGAGAGGCACCCACTTTTTCCCTCTCCAGGATGATAGGGTATCATGATGCTTCCTGCCCCCGCACCTTCCCCTCAGAGGCCTTTTCACCAAAGGTGCACCAGATTTCCAGTCGCCTCGTGTGTAAGCTGCAGGTAGGATGTCCGACCCCCTTT... |
Task1_train_41340 | A mutation found on Chromosome 11 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GCCTCAGTTTTCTTATTTGTAGACTGAGGAGAATGGATGCTGGGCCCCAGAGAGGAGGGAAAAGCACATGGTGATGCTCTGCGAATTGTAAAGGACCCGACCAGGGGTTCTGACCAGGCCAGTGGTGCCCAGGTGCCTCAGCTGAGCATTCTCTCTCCACAGGTGACCCGTTGCCTGCCCGCCAGGAAGGTGTGAAGAAGAAGGCAGCTGAGTACCTGAAGCGGGCAGAGGAGATCCTGCGCCTGCACCTGTCTCAACTCCCACCCTAACAGGGAGTGGGCCATTCCCTGGGACTCTCGCTCCTGCACTGCCAGCCCCTT... | GCCTCAGTTTTCTTATTTGTAGACTGAGGAGAATGGATGCTGGGCCCCAGAGAGGAGGGAAAAGCACATGGTGATGCTCTGCGAATTGTAAAGGACCCGACCAGGGGTTCTGACCAGGCCAGTGGTGCCCAGGTGCCTCAGCTGAGCATTCTCTCTCCACAGGTGACCCGTTGCCTGCCCGCCAGGAAGGTGTGAAGAAGAAGGCAGCTGAGTACCTGAAGCGGGCAGAGGAGATCCTGCGCCTGCACCTGTCTCAACTCCCACCCTAACAGGGAGTGGGCCATTCCCTGGGACTCTCGCTCCTGCACTGCCAGCCCCTT... |
Task1_train_41341 | A variant was discovered on Chromosome 11. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CGCAAAAAAAAAAAAAAAAAAAGCATAATTAGTCTCTCTCTGTGTCCTTTTAAAGGAAACATCAAATGGGACCATGCTGATGACTGCATCTTATTGACAGAAGTCCTTAAATGGGTAATTGATTTAGCTGTTGATCCAACTACCATCAACCTCAGTACCCTATGATTCCCTTTGGGAAAATTGCAAGACAGCTGTTTGTACAGCAGGGCCCCTGGTCAAGGACAGGTCAGGAAGTAGGTGGTTGGGGAGGTCTGGGATCCCTACAGCCATCGGGTGAGGAGGGTAGAGTCTCAGAAGGGGTGGGCTGCTAAGTCAGAGAT... | CGCAAAAAAAAAAAAAAAAAAAGCATAATTAGTCTCTCTCTGTGTCCTTTTAAAGGAAACATCAAATGGGACCATGCTGATGACTGCATCTTATTGACAGAAGTCCTTAAATGGGTAATTGATTTAGCTGTTGATCCAACTACCATCAACCTCAGTACCCTATGATTCCCTTTGGGAAAATTGCAAGACAGCTGTTTGTACAGCAGGGCCCCTGGTCAAGGACAGGTCAGGAAGTAGGTGGTTGGGGAGGTCTGGGATCCCTACAGCCATCGGGTGAGGAGGGTAGAGTCTCAGAAGGGGTGGGCTGCTAAGTCAGAGAT... |
Task1_train_41342 | A variant affecting Chromosome 11 has been observed. Determine if it's benign or associated with disease. | Benign | ACACGGCACCTGCCGGCTATCAGTGCCCCAGCTGCAATGGCCCCATCTTCCCCCCAACCAACCTGGCTGGCCCCGTGGCCTCCGCACTGAGAGAGAAGCTGGCCACAGTCAACTGGGCCCGGGCAGGACTGGGCCTCCCTCTGGTGAGAGTCCCTCGTCTGTCTGACCATCTATCTGCCCTGGGCCCCACCTGAGTCAGATGGGTGGGTGGGGACAATACTAGGCAGCCTGGTGACCCAGATTCCTTCCTCCAGATCGATGAGGTGGTGAGCCCAGAGCCCGAGCCCCTCAACACGTCTGACTTCTCTGACTGGTCTAGT... | ACACGGCACCTGCCGGCTATCAGTGCCCCAGCTGCAATGGCCCCATCTTCCCCCCAACCAACCTGGCTGGCCCCGTGGCCTCCGCACTGAGAGAGAAGCTGGCCACAGTCAACTGGGCCCGGGCAGGACTGGGCCTCCCTCTGGTGAGAGTCCCTCGTCTGTCTGACCATCTATCTGCCCTGGGCCCCACCTGAGTCAGATGGGTGGGTGGGGACAATACTAGGCAGCCTGGTGACCCAGATTCCTTCCTCCAGATCGATGAGGTGGTGAGCCCAGAGCCCGAGCCCCTCAACACGTCTGACTTCTCTGACTGGTCTAGT... |
Task1_train_41343 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AGCGGGGCTGCCTCTGGGGGCGCTCCCGGAAATGCTCCTGCCCTTGGCGTTTGTCGCCACCCTCACCGCTTTCATCTTCAGCCTCTTTCTCTACATGAAGGCGCAGGTAGCCCCAGTTTCGGCCCTGGCACCTGGGGGGAACTCAGGTGAGAGGGGTCCTGGGGTGGAGACGGAGGCAGATTGGGGCGTCTGCCTGTACATTCACTCTCCAATATTCTCCAGGCAATCCGATTTACGACTTTTTTCTGGGACGAGAGCTCAACCCTCGTATCTGTTTCTTCGACTTCAAATATTTCTGTGAACTGCGACCCGGCCTCATC... | AGCGGGGCTGCCTCTGGGGGCGCTCCCGGAAATGCTCCTGCCCTTGGCGTTTGTCGCCACCCTCACCGCTTTCATCTTCAGCCTCTTTCTCTACATGAAGGCGCAGGTAGCCCCAGTTTCGGCCCTGGCACCTGGGGGGAACTCAGGTGAGAGGGGTCCTGGGGTGGAGACGGAGGCAGATTGGGGCGTCTGCCTGTACATTCACTCTCCAATATTCTCCAGGCAATCCGATTTACGACTTTTTTCTGGGACGAGAGCTCAACCCTCGTATCTGTTTCTTCGACTTCAAATATTTCTGTGAACTGCGACCCGGCCTCATC... |
Task1_train_41344 | A genomic variant on Chromosome 11 is under review. What is the biological outcome — benign or pathogenic? | Benign | TTAAATATACAATTTAAATATACTATTTAAAGTATATTCACAGAGTTGTGCAACCATCACCACATCAATTTTAGAACATTTCATTATCCCAAAAACAAATGAGGTACTCCTTAGCCATGACTCCCCAGCCCTCCCAGCAGCCCTGGCAACCACAAATCTACTTCTTATCTCTATGGATTTGCCTACTGGGATATTTCATGTGAACAGGATCATATAATACATGGTCCTTTGTGGCTGGCCTTTTTCATTTAGCATAATGTTTGCAAGGTTCCTCCATGTTGTAGCATGGATCAGAATGTTGTTCCTCTTTGTTGCCAAAT... | TTAAATATACAATTTAAATATACTATTTAAAGTATATTCACAGAGTTGTGCAACCATCACCACATCAATTTTAGAACATTTCATTATCCCAAAAACAAATGAGGTACTCCTTAGCCATGACTCCCCAGCCCTCCCAGCAGCCCTGGCAACCACAAATCTACTTCTTATCTCTATGGATTTGCCTACTGGGATATTTCATGTGAACAGGATCATATAATACATGGTCCTTTGTGGCTGGCCTTTTTCATTTAGCATAATGTTTGCAAGGTTCCTCCATGTTGTAGCATGGATCAGAATGTTGTTCCTCTTTGTTGCCAAAT... |
Task1_train_41345 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | GCGAGACGGGTGCGGCTCCTTGGCTGAGGTTTGAGATTCAGGTCAGCCTGGCTACACACCCGCCTCATGATGGTGCCAACTTTGCATCCTCTTGCACAGTACGGTGCTGGCTAATGGCCTTCCTTGATCTTGATTATGAGGGATTCCTGTGCTTTCCCTTCTCAACCTGGTGTCCTGCGTCCCTCCTCATGTGGGGACAGACTGAGCTCCTTGTGGGTGGGTCTTTAAACTTCCCCAGAGGCATCCTCCTCTTGTTGCTGTGCCTTGGCCATTTACCTTCTCTCTGGTTTATTAAATTCTCCAGTCCTCCCTGAAGAGAA... | GCGAGACGGGTGCGGCTCCTTGGCTGAGGTTTGAGATTCAGGTCAGCCTGGCTACACACCCGCCTCATGATGGTGCCAACTTTGCATCCTCTTGCACAGTACGGTGCTGGCTAATGGCCTTCCTTGATCTTGATTATGAGGGATTCCTGTGCTTTCCCTTCTCAACCTGGTGTCCTGCGTCCCTCCTCATGTGGGGACAGACTGAGCTCCTTGTGGGTGGGTCTTTAAACTTCCCCAGAGGCATCCTCCTCTTGTTGCTGTGCCTTGGCCATTTACCTTCTCTCTGGTTTATTAAATTCTCCAGTCCTCCCTGAAGAGAA... |
Task1_train_41346 | A sequence alteration has been identified on Chromosome 11. Is it disease-inducing or harmless? | Benign | GAAACAAACTTTTATCCCTAAGTGCTTTACTCTTTTATCACAAAAGTTTGTGTCACAGTTTTTTGGTCCCTGAGGTTACACAGTGAAGCACACTTAGTCTCTGCCAACAGAGAAGATAAGAATACATGTAAAAATAACAGCTATAAATATGCCAGCATTGGGTTAAGTGCCTTTTCATGCCCTTTCTCCTTTAGTCTGTACAACCTTATGGGGTAGGTCCTGTGTTCCCCATTTCACACAGAGGCTGAAACAAAGCAGTTTAAAAACTTCCCATGGGTCGGGCACGGTAGCTCACGCCTGTAATCCCAGCACTTTGGGAG... | GAAACAAACTTTTATCCCTAAGTGCTTTACTCTTTTATCACAAAAGTTTGTGTCACAGTTTTTTGGTCCCTGAGGTTACACAGTGAAGCACACTTAGTCTCTGCCAACAGAGAAGATAAGAATACATGTAAAAATAACAGCTATAAATATGCCAGCATTGGGTTAAGTGCCTTTTCATGCCCTTTCTCCTTTAGTCTGTACAACCTTATGGGGTAGGTCCTGTGTTCCCCATTTCACACAGAGGCTGAAACAAAGCAGTTTAAAAACTTCCCATGGGTCGGGCACGGTAGCTCACGCCTGTAATCCCAGCACTTTGGGAG... |
Task1_train_41347 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | CGCCGCCCGGACAGGGGCTCGGGAGCCGGGCTGGGGGCAGGGGCTGGAGCCGCGGGACCAGCGCCTGAGGTGGGTGCGGAGCGGGAGGCCGGGCGGGCGGGCGCCTGGGGCCGCCCCGCCGACATACTCCGGGTCGAGGGGGAGTGACCGGCCAGGGCACGGAGTCCGGCTGCCGGCCTGCCTGGGTCCGGGCGTTCGTTCCCGCGCCCTGGGACCCTCCCAGGCCACCACCCTCCCCGCGGGGACACCCCGCCCCTCCGCTGCCCGCAGCCTCCTCAGGCCTCCCGCCCTTTGTCGCTCGTGCACCTGCGCCCTCGGCC... | CGCCGCCCGGACAGGGGCTCGGGAGCCGGGCTGGGGGCAGGGGCTGGAGCCGCGGGACCAGCGCCTGAGGTGGGTGCGGAGCGGGAGGCCGGGCGGGCGGGCGCCTGGGGCCGCCCCGCCGACATACTCCGGGTCGAGGGGGAGTGACCGGCCAGGGCACGGAGTCCGGCTGCCGGCCTGCCTGGGTCCGGGCGTTCGTTCCCGCGCCCTGGGACCCTCCCAGGCCACCACCCTCCCCGCGGGGACACCCCGCCCCTCCGCTGCCCGCAGCCTCCTCAGGCCTCCCGCCCTTTGTCGCTCGTGCACCTGCGCCCTCGGCC... |
Task1_train_41348 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | ACCCCATGTCTACTAAAAATACACAAAAAAATTAGCCGGGTGTGGTGGTGGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGTGGAGCTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAATCTCAAAAAATAAAAAATAAAAATAAAAATAAAAAAATCAGAGTAGAAGGAAGGAGTTCTGAGGGTTGTGATAATAAGTAGGGTGGCAATGATAGAAGGCTTTCTGAACAGATTTTGAAAGATGGTTATGGGCTGGGA... | ACCCCATGTCTACTAAAAATACACAAAAAAATTAGCCGGGTGTGGTGGTGGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGTGGAGCTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAATCTCAAAAAATAAAAAATAAAAATAAAAATAAAAAAATCAGAGTAGAAGGAAGGAGTTCTGAGGGTTGTGATAATAAGTAGGGTGGCAATGATAGAAGGCTTTCTGAACAGATTTTGAAAGATGGTTATGGGCTGGGA... |
Task1_train_41349 | A mutation found on Chromosome 11 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GGGGGTGAGGCCAAGAATTAGGGGGGCCTGCTCAGCATCACTGGCCCAGGAGGTCTCCTTGGAGGAGGCAGCATTTACCCAACACATGCAGCATGAGAGGCAGCTGGGACCAGAACTTGGGGTGCATCCCAGGAGGAGGTAGCAACCACCGCGTGCACCTGTAATCCCAGCTACTTGGGAGGCTGAGGCACGAGAATTGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCACCCCTGCACTCCAGCCTCGACGACAGAGGAAGACTCCGTCTCAAAAAAAAAAAAAAAGCCACCACTACCAAGCACCTCC... | GGGGGTGAGGCCAAGAATTAGGGGGGCCTGCTCAGCATCACTGGCCCAGGAGGTCTCCTTGGAGGAGGCAGCATTTACCCAACACATGCAGCATGAGAGGCAGCTGGGACCAGAACTTGGGGTGCATCCCAGGAGGAGGTAGCAACCACCGCGTGCACCTGTAATCCCAGCTACTTGGGAGGCTGAGGCACGAGAATTGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCACCCCTGCACTCCAGCCTCGACGACAGAGGAAGACTCCGTCTCAAAAAAAAAAAAAAAGCCACCACTACCAAGCACCTCC... |
Task1_train_41350 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | CTGCTGCGGGAGGGCCGTGCCACGTGAGTGCCTACCTGCCCTCCTTGATCCTGGCCTGTGACCTCTGACTCCACCCTCACCTTTAACCTCTGCCTCCCAGGGACGATGACATGCAGAGTCTCGCAAGCCTCATGAGTGTGAAGCCTAGTGATGTGGGCAACTTGGATGACTTTGCTGAGAGTGATGAAGATGAGGCTCATGGCCCAGGAGCCCCGGAGGCCCGGGCTCGAGTCCCCCAGCCAGGTGGGCTCACAGCCTGCTGTGGATCGAGACTGCCAAGACCTGGGGAGGGAGGGTTACCCGGGCCACCAGCCACTTGC... | CTGCTGCGGGAGGGCCGTGCCACGTGAGTGCCTACCTGCCCTCCTTGATCCTGGCCTGTGACCTCTGACTCCACCCTCACCTTTAACCTCTGCCTCCCAGGGACGATGACATGCAGAGTCTCGCAAGCCTCATGAGTGTGAAGCCTAGTGATGTGGGCAACTTGGATGACTTTGCTGAGAGTGATGAAGATGAGGCTCATGGCCCAGGAGCCCCGGAGGCCCGGGCTCGAGTCCCCCAGCCAGGTGGGCTCACAGCCTGCTGTGGATCGAGACTGCCAAGACCTGGGGAGGGAGGGTTACCCGGGCCACCAGCCACTTGC... |
Task1_train_41351 | A genetic alteration is present on Chromosome 11. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GGTCTGTGTACTGGTTGTGTGGAGAGGTGATGAAATTTTCTTGTGAGTCTGTGAATCCCAGCTATGATGTTGATGGCAGGTACATCCTGTGGGGGCGAGGCTTTGTGAAAAGGGACCTGGCTTACTTTCATCTTCAGGTCCTGCCTCCCAGCTTGATGGTGGCCGGCGTGTACTGCCTCGTGGTGGCTGTCATCTTTGCTACTATCAAGACTGTCAATTATCGGCTTCATGCCATGTTTGACCAGGGCGAGATCGTGGAGAAGCGCAGCTCTACCATGGGGGAGCTGGAGGAAGAGCCTGCCCAGGGGGACAGCAATCCA... | GGTCTGTGTACTGGTTGTGTGGAGAGGTGATGAAATTTTCTTGTGAGTCTGTGAATCCCAGCTATGATGTTGATGGCAGGTACATCCTGTGGGGGCGAGGCTTTGTGAAAAGGGACCTGGCTTACTTTCATCTTCAGGTCCTGCCTCCCAGCTTGATGGTGGCCGGCGTGTACTGCCTCGTGGTGGCTGTCATCTTTGCTACTATCAAGACTGTCAATTATCGGCTTCATGCCATGTTTGACCAGGGCGAGATCGTGGAGAAGCGCAGCTCTACCATGGGGGAGCTGGAGGAAGAGCCTGCCCAGGGGGACAGCAATCCA... |
Task1_train_41352 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | CCACAAGGGCCACAGTCCTGCCCCCACCTGGTCTCCCGGGGCTCAGACAGCAGCCGCCAGCCCACGGAGGTAGTCCCCCGCCAGGGGCAGCACGGCCCAGTCATCGGTCCGCAGGGCCACAGGCACTCCATCTGCCAGGGCCGCCTCCAGCCGCAGCAGCAGCTTTGAGTCCGGGGGCAGGTGGATTGCTACACAGTAGCTGGTAGGAGGCTGGGCCACCACCACAAAAGGCTCCAGGTGGCGGGACACCAAGCCCTCCAGGCCCTGTGGCCCAAGTGGACACCACACACGACTCTCAGCACCCTCTGGCAGGCAGGAAT... | CCACAAGGGCCACAGTCCTGCCCCCACCTGGTCTCCCGGGGCTCAGACAGCAGCCGCCAGCCCACGGAGGTAGTCCCCCGCCAGGGGCAGCACGGCCCAGTCATCGGTCCGCAGGGCCACAGGCACTCCATCTGCCAGGGCCGCCTCCAGCCGCAGCAGCAGCTTTGAGTCCGGGGGCAGGTGGATTGCTACACAGTAGCTGGTAGGAGGCTGGGCCACCACCACAAAAGGCTCCAGGTGGCGGGACACCAAGCCCTCCAGGCCCTGTGGCCCAAGTGGACACCACACACGACTCTCAGCACCCTCTGGCAGGCAGGAAT... |
Task1_train_41353 | A variant on Chromosome 11 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GCACTCCATCTGCCAGGGCCGCCTCCAGCCGCAGCAGCAGCTTTGAGTCCGGGGGCAGGTGGATTGCTACACAGTAGCTGGTAGGAGGCTGGGCCACCACCACAAAAGGCTCCAGGTGGCGGGACACCAAGCCCTCCAGGCCCTGTGGCCCAAGTGGACACCACACACGACTCTCAGCACCCTCTGGCAGGCAGGAATCCCAGAGCTCCTCAAAGAAGCCCAGCCCGGCCCCCTCTGGAGGCTGCGGGAAAGGCAGAAAGAGGTCGGCAAAGTTCACGAACAGGGGTGGCAAGTGGGCATGGCACGTGAGACCAGTGGAT... | GCACTCCATCTGCCAGGGCCGCCTCCAGCCGCAGCAGCAGCTTTGAGTCCGGGGGCAGGTGGATTGCTACACAGTAGCTGGTAGGAGGCTGGGCCACCACCACAAAAGGCTCCAGGTGGCGGGACACCAAGCCCTCCAGGCCCTGTGGCCCAAGTGGACACCACACACGACTCTCAGCACCCTCTGGCAGGCAGGAATCCCAGAGCTCCTCAAAGAAGCCCAGCCCGGCCCCCTCTGGAGGCTGCGGGAAAGGCAGAAAGAGGTCGGCAAAGTTCACGAACAGGGGTGGCAAGTGGGCATGGCACGTGAGACCAGTGGAT... |
Task1_train_41354 | Consider this mutation on Chromosome 11. Is this a benign change or a disease-causing variant? | Benign | AAGATGTTTGGCAAAGTCATGAGGCGTTAAAGGGTAAAGACGAGGGTTTGTGCATTCAATTCAAGGCTTCTTTACATGCCTTTACGTGCCAATGAGAAGAAATAGATATTAAACCAGACTTGAACCCAGCTCTCGAGTTGATAGCCAGGTACATGGTTATTCTAACATCCGCAAAACTGAGACAAGTTCTGTGGTAGTATATGCCTTAAAAAAAAAAAGAAACGAGCGGGGGACTCCGGGATGATTTTGTTGTTCTAGAACAGTGACCACAGCCTCACACTCTGCAGGAAAAGACTGGGTCGCAAACAAGTCAGAGGCAA... | AAGATGTTTGGCAAAGTCATGAGGCGTTAAAGGGTAAAGACGAGGGTTTGTGCATTCAATTCAAGGCTTCTTTACATGCCTTTACGTGCCAATGAGAAGAAATAGATATTAAACCAGACTTGAACCCAGCTCTCGAGTTGATAGCCAGGTACATGGTTATTCTAACATCCGCAAAACTGAGACAAGTTCTGTGGTAGTATATGCCTTAAAAAAAAAAAGAAACGAGCGGGGGACTCCGGGATGATTTTGTTGTTCTAGAACAGTGACCACAGCCTCACACTCTGCAGGAAAAGACTGGGTCGCAAACAAGTCAGAGGCAA... |
Task1_train_41355 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | CGCTCTCGAATCTGGGGTGACAGGAAGGAGCCGGTCCAGGCTCCGGGGGCTGGGAAAGGGCGCGTCTCAAAGGCTGGCTGGAGTGGAGCCAAGGGAAAAGATCGTTAGAGACAGCGCCCCTGACCAACCACTTAGAGCAGCGCAGGGGTGGGAGGGCGGCCGCAGGCTCTCCTCTCGTTAGTGCCCCCTGTGTTTGGGGCCCCGTGATCTCAACGGTCCTGCCCTCGGTCTCCCTCTTCCCCCGCCCCGCCCTGGGCCAGGTGTTCGAATCCCGACTCCAGAACTGGCGGCGTCCCAGTCCCGCGGGCGTGGAGCGCCGG... | CGCTCTCGAATCTGGGGTGACAGGAAGGAGCCGGTCCAGGCTCCGGGGGCTGGGAAAGGGCGCGTCTCAAAGGCTGGCTGGAGTGGAGCCAAGGGAAAAGATCGTTAGAGACAGCGCCCCTGACCAACCACTTAGAGCAGCGCAGGGGTGGGAGGGCGGCCGCAGGCTCTCCTCTCGTTAGTGCCCCCTGTGTTTGGGGCCCCGTGATCTCAACGGTCCTGCCCTCGGTCTCCCTCTTCCCCCGCCCCGCCCTGGGCCAGGTGTTCGAATCCCGACTCCAGAACTGGCGGCGTCCCAGTCCCGCGGGCGTGGAGCGCCGG... |
Task1_train_41356 | A mutation found on Chromosome 11 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | AACCCAGGGCCTCCTGGCGCTGTCCAGAGTGGAGTTTCTTAGGACCCCTGCAAGCCAGCCAAGTCCAAATCTCTGGGCCGGGGCCTGGAGTCCGCCCTCCTCGTTACCTCCTCTCCTCTCGGGGTGACTGAAGCTCGTGGTGCAGAGCTCCCAGCTCCTGTCAATGGGGGCCCCTGGGCCTGAACATATAGAGACCCCCATTTAGGTGAACTTGGCCTGCCCCCCCAAGTGCCACCCTGCCCCAGCCTGAGGCTTCCTGCAGTGTGACCCGCCCACCTCAGCCACCAGGACTTTCTTTCTCCCTTTATTGCCTTTCTCAT... | AACCCAGGGCCTCCTGGCGCTGTCCAGAGTGGAGTTTCTTAGGACCCCTGCAAGCCAGCCAAGTCCAAATCTCTGGGCCGGGGCCTGGAGTCCGCCCTCCTCGTTACCTCCTCTCCTCTCGGGGTGACTGAAGCTCGTGGTGCAGAGCTCCCAGCTCCTGTCAATGGGGGCCCCTGGGCCTGAACATATAGAGACCCCCATTTAGGTGAACTTGGCCTGCCCCCCCAAGTGCCACCCTGCCCCAGCCTGAGGCTTCCTGCAGTGTGACCCGCCCACCTCAGCCACCAGGACTTTCTTTCTCCCTTTATTGCCTTTCTCAT... |
Task1_train_41357 | Consider this mutation on Chromosome 11. Is this a benign change or a disease-causing variant? | Benign | CCAGTTCAACCGGAGTTACCTGAGCCCAGAAGGTATCACAGGGCACATACATCTCCAGTCCAAGCCCCCACTTTTTTTTTTTTTGAGACGGAGTTTCACTCTTGTTGACCAGGCTGGAGTGCAATGGTGTCATCTTGGCTCACTGCAACCTCCACCTCCCGGGTTCAAGCGATTCTCCTGCTTCAGCCTCTGAGTAGCTGGGATTACAGGCATGCGCCACCACACTTGGCTAACCTTTACATTTTTAGTAGAGATGGGGTTTGACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACATCAGGTGATCCGCCTGCCTCGG... | CCAGTTCAACCGGAGTTACCTGAGCCCAGAAGGTATCACAGGGCACATACATCTCCAGTCCAAGCCCCCACTTTTTTTTTTTTTGAGACGGAGTTTCACTCTTGTTGACCAGGCTGGAGTGCAATGGTGTCATCTTGGCTCACTGCAACCTCCACCTCCCGGGTTCAAGCGATTCTCCTGCTTCAGCCTCTGAGTAGCTGGGATTACAGGCATGCGCCACCACACTTGGCTAACCTTTACATTTTTAGTAGAGATGGGGTTTGACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACATCAGGTGATCCGCCTGCCTCGG... |
Task1_train_41358 | Given this context: Chromosome 11 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | CACCAGGCTCCAACTCGGAGACCACCCAGCTCTGGGGACTTCCCAAGGCTGGGCAGAGGGGGACTCAGCCCTGGGGAAGCTCAGGGTGGGGAGGAAGCTGGAGAGAGCACTGAGCCAGCATCTCATGACTCAGCCACTTCCACCCAGTCAGCCCGGTGGCATCTCCGCTCCCCTGCTCTAAATTCCGATTCGGTGAGACTGCTGGAGGCTGAGTCAGTCCCGGCACGGCACGAGAGCTGTGTCCCAAGGGGCTCCCTGCCAGACACCCTGGCCCCCAATCAAGGCCAGGGCCAGGCACGGGGCTGGAGAGGTGGCGGGGT... | CACCAGGCTCCAACTCGGAGACCACCCAGCTCTGGGGACTTCCCAAGGCTGGGCAGAGGGGGACTCAGCCCTGGGGAAGCTCAGGGTGGGGAGGAAGCTGGAGAGAGCACTGAGCCAGCATCTCATGACTCAGCCACTTCCACCCAGTCAGCCCGGTGGCATCTCCGCTCCCCTGCTCTAAATTCCGATTCGGTGAGACTGCTGGAGGCTGAGTCAGTCCCGGCACGGCACGAGAGCTGTGTCCCAAGGGGCTCCCTGCCAGACACCCTGGCCCCCAATCAAGGCCAGGGCCAGGCACGGGGCTGGAGAGGTGGCGGGGT... |
Task1_train_41359 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AACACAGGCAGAGTAGGGACAGGGGACTTACACCAGGTCACACGGGGAGCCTGTGGATGAGGCAGAGGCAGGACTTGGGCCTGGGTCTCTGCGCTAAATGACTCCTGGGCATCCTGCTGAACTCTCTCCCAGAAGGAGATTGGCCTCACATACCCCACTGACCCCTTCCTAGCATGCTTTTTGCCAGACCCATTGAGACTGGCTGAGGACTGGTTGCCATAGAGATGGCCTGTTAGGCAGTTCTACGGTGCGGATGGGGGATGGGGCAGGATGGGGCAGGACACCGATATGCTAAATACCTACCAACAGTTGGTTAGGAC... | AACACAGGCAGAGTAGGGACAGGGGACTTACACCAGGTCACACGGGGAGCCTGTGGATGAGGCAGAGGCAGGACTTGGGCCTGGGTCTCTGCGCTAAATGACTCCTGGGCATCCTGCTGAACTCTCTCCCAGAAGGAGATTGGCCTCACATACCCCACTGACCCCTTCCTAGCATGCTTTTTGCCAGACCCATTGAGACTGGCTGAGGACTGGTTGCCATAGAGATGGCCTGTTAGGCAGTTCTACGGTGCGGATGGGGGATGGGGCAGGATGGGGCAGGACACCGATATGCTAAATACCTACCAACAGTTGGTTAGGAC... |
Task1_train_41360 | Given this context: Chromosome 11 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | TCCATGGGTGCTGCCTCCACACCTCAAGGCCTCTCTTACATGCTTCACAGATGGATGCCTGGTCCCATGTGGGTGTGGCTCGAAGGTCCCTCTTGCTGCTAGAGTGCTCTCTTCATGAGTGGCAGTGATACTCAAGTTTGTCAAACAGACACATTTCTGACAAGTGCACAAACTGGGTTTTGGGTTTTTTGAGACAGGGTCTTGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTCACTGTAGCCTAGACCTCCGAGGCTCAAGCGATCCTCCCACCTTGGCCTCCCAACTACCCAGGACTACAGGTGCA... | TCCATGGGTGCTGCCTCCACACCTCAAGGCCTCTCTTACATGCTTCACAGATGGATGCCTGGTCCCATGTGGGTGTGGCTCGAAGGTCCCTCTTGCTGCTAGAGTGCTCTCTTCATGAGTGGCAGTGATACTCAAGTTTGTCAAACAGACACATTTCTGACAAGTGCACAAACTGGGTTTTGGGTTTTTTGAGACAGGGTCTTGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTCACTGTAGCCTAGACCTCCGAGGCTCAAGCGATCCTCCCACCTTGGCCTCCCAACTACCCAGGACTACAGGTGCA... |
Task1_train_41361 | A variant on Chromosome 11 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TTCCTGAGACTGTTGTCATATTTTGTTTGTTGTTGTTGTTGTTTTCTGAGATGGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTATCGTGATCTCGGCTCACTACAACCTCCGCCTCCCAGCTTCAAGAGATTCTCCTGCCTCACCCTCCTGTGTAGCCAGGATTACAGGCACGCACCACCACACCCGGCTAATTTTTGTATTTTTTTGGTAGAGACAGGGTTTTGCCATATTGGCCAGGCTGGTCTCCAACTCCTGACCTCAAGCAATCTACCTACCTTGGACTCCCAAAATGTTAGGATTACAGATGTGAGCCAT... | TTCCTGAGACTGTTGTCATATTTTGTTTGTTGTTGTTGTTGTTTTCTGAGATGGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTATCGTGATCTCGGCTCACTACAACCTCCGCCTCCCAGCTTCAAGAGATTCTCCTGCCTCACCCTCCTGTGTAGCCAGGATTACAGGCACGCACCACCACACCCGGCTAATTTTTGTATTTTTTTGGTAGAGACAGGGTTTTGCCATATTGGCCAGGCTGGTCTCCAACTCCTGACCTCAAGCAATCTACCTACCTTGGACTCCCAAAATGTTAGGATTACAGATGTGAGCCAT... |
Task1_train_41362 | An alteration has been detected on Chromosome 11. Is it pathogenic, and if so, what disease is involved? | Benign | GTGAGCCGAGATTGCACCACTGCACTCCAGACTGGGTGACAGAGTGAGACTGTCTAGAAAAAAAAAAAGTAGACTTAAAGGCACGTCTGAATTTTCCAGGCCAACTGAGGGCAAGGTGAAGGATTTTCCTGGCAGAGGTATGACCAGAGGCTAGGGCTGGGGGTGCAGATGGAGACAATGGCAAGCACCTTATTGGCTGGGGGCCAGAGGACACCTGTTTTTGGATAGATCACTTTGAGTCTGGTACAATTCTTTACTGCTGCTTAATGTCAGAAACTTAATTATGCTTTTGCATGATTCTAATTATTGCCTTTTTCAGA... | GTGAGCCGAGATTGCACCACTGCACTCCAGACTGGGTGACAGAGTGAGACTGTCTAGAAAAAAAAAAAGTAGACTTAAAGGCACGTCTGAATTTTCCAGGCCAACTGAGGGCAAGGTGAAGGATTTTCCTGGCAGAGGTATGACCAGAGGCTAGGGCTGGGGGTGCAGATGGAGACAATGGCAAGCACCTTATTGGCTGGGGGCCAGAGGACACCTGTTTTTGGATAGATCACTTTGAGTCTGGTACAATTCTTTACTGCTGCTTAATGTCAGAAACTTAATTATGCTTTTGCATGATTCTAATTATTGCCTTTTTCAGA... |
Task1_train_41363 | Here is a genetic alteration on Chromosome 11. Based on the data, is it a benign variant or a cause of disease? | Benign | CAGCAGAGGCTTGAGTACAACCCAGGGAGAGACGAAGGAAGGGGCTAGTAGCTCAGGGAAAGCACAGCACCCCAACTAGCCCTTTTGGGGTTCTCCTGATCCTAGAAGGAAGGAACTGGGGACTCCCAAGCCTCCTGGGTTTGGGCTTTGCATTATGGTGTGTCGGGGGCCTTGAGGAGATTCTCCCTTGACAAGCAGAGAAAAGACCTGCAGCTCCTCACTGTAGGGCCAGGCCTGGCCCTTCACTGGGTGCCAGAGCCCAACTAGGCCCAGGCTACAGTCATAGGCGAGGGGGTCGACAGGCCTCCGACCCTTACCTG... | CAGCAGAGGCTTGAGTACAACCCAGGGAGAGACGAAGGAAGGGGCTAGTAGCTCAGGGAAAGCACAGCACCCCAACTAGCCCTTTTGGGGTTCTCCTGATCCTAGAAGGAAGGAACTGGGGACTCCCAAGCCTCCTGGGTTTGGGCTTTGCATTATGGTGTGTCGGGGGCCTTGAGGAGATTCTCCCTTGACAAGCAGAGAAAAGACCTGCAGCTCCTCACTGTAGGGCCAGGCCTGGCCCTTCACTGGGTGCCAGAGCCCAACTAGGCCCAGGCTACAGTCATAGGCGAGGGGGTCGACAGGCCTCCGACCCTTACCTG... |
Task1_train_41364 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | CCAGGGAGAGACGAAGGAAGGGGCTAGTAGCTCAGGGAAAGCACAGCACCCCAACTAGCCCTTTTGGGGTTCTCCTGATCCTAGAAGGAAGGAACTGGGGACTCCCAAGCCTCCTGGGTTTGGGCTTTGCATTATGGTGTGTCGGGGGCCTTGAGGAGATTCTCCCTTGACAAGCAGAGAAAAGACCTGCAGCTCCTCACTGTAGGGCCAGGCCTGGCCCTTCACTGGGTGCCAGAGCCCAACTAGGCCCAGGCTACAGTCATAGGCGAGGGGGTCGACAGGCCTCCGACCCTTACCTGGGCTGGTTGCACAGGTGATCT... | CCAGGGAGAGACGAAGGAAGGGGCTAGTAGCTCAGGGAAAGCACAGCACCCCAACTAGCCCTTTTGGGGTTCTCCTGATCCTAGAAGGAAGGAACTGGGGACTCCCAAGCCTCCTGGGTTTGGGCTTTGCATTATGGTGTGTCGGGGGCCTTGAGGAGATTCTCCCTTGACAAGCAGAGAAAAGACCTGCAGCTCCTCACTGTAGGGCCAGGCCTGGCCCTTCACTGGGTGCCAGAGCCCAACTAGGCCCAGGCTACAGTCATAGGCGAGGGGGTCGACAGGCCTCCGACCCTTACCTGGGCTGGTTGCACAGGTGATCT... |
Task1_train_41365 | This is a variant located on Chromosome 11. Is this mutation a likely cause of disease or not? | Benign | GCTGAGCCATTGTGCAAGCGGGCACTGGAGATCCGGGAGAAGGTGGGAACAGGCAGGGCTGGGCAGGCTGGGGGTCTGGGAGGCAGGGGCCCGGGCAGCCCTGAGCCCAACCCCTGGCTCCCTCTCCCATCCCAGGTCCTGGGCAAGTTTCACCCAGATGTGGCCAAGCAGCTCAGCAACCTGGCCCTGCTGTGCCAGAACCAGGGCAAAGCTGAGGAGGTGGAATATTACTATCGGCGGGCACTGGAGATCTATGCTACACGCCTCGGGCCCGATGACCCCAATGTGGCCAAGACCAAGAACAACCTGGTACCTTGGGG... | GCTGAGCCATTGTGCAAGCGGGCACTGGAGATCCGGGAGAAGGTGGGAACAGGCAGGGCTGGGCAGGCTGGGGGTCTGGGAGGCAGGGGCCCGGGCAGCCCTGAGCCCAACCCCTGGCTCCCTCTCCCATCCCAGGTCCTGGGCAAGTTTCACCCAGATGTGGCCAAGCAGCTCAGCAACCTGGCCCTGCTGTGCCAGAACCAGGGCAAAGCTGAGGAGGTGGAATATTACTATCGGCGGGCACTGGAGATCTATGCTACACGCCTCGGGCCCGATGACCCCAATGTGGCCAAGACCAAGAACAACCTGGTACCTTGGGG... |
Task1_train_41366 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | CCAAGAGGCTGTAACTGAAAAATTACAGAGGCGGTGGGAACTGGCGCCTCCCCTCCCCAGGTCTCACCCCCGCCCCCCAAGGCAGTGAGCACGAAATGAGGGAGGTCACTCCCACCAGGCTGTGATCTTTGACCAGGCCCTCCAGTTCCTGGGACACTTCAGTCCTGAGCAGCCGGAGCCCTCGCTCAAGCTCAGGTCTGCTGAGCTCTGTCTGTCCCCCACCACCCCCAGCCAACATGGACAAGAGCAACGTGCGGCCCTGGCAAAAGGAGGCCTTGCTCCTGCGGCTGTCCAAGCAGTTAGCATGGGATCTCTCCCAG... | CCAAGAGGCTGTAACTGAAAAATTACAGAGGCGGTGGGAACTGGCGCCTCCCCTCCCCAGGTCTCACCCCCGCCCCCCAAGGCAGTGAGCACGAAATGAGGGAGGTCACTCCCACCAGGCTGTGATCTTTGACCAGGCCCTCCAGTTCCTGGGACACTTCAGTCCTGAGCAGCCGGAGCCCTCGCTCAAGCTCAGGTCTGCTGAGCTCTGTCTGTCCCCCACCACCCCCAGCCAACATGGACAAGAGCAACGTGCGGCCCTGGCAAAAGGAGGCCTTGCTCCTGCGGCTGTCCAAGCAGTTAGCATGGGATCTCTCCCAG... |
Task1_train_41367 | This mutation on Chromosome 11 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GGAGACGCCTGAGAGAGGAGGGAAGTGAGGTGCTTCTCTGGGGAACCTCCCTGCTTCCAGCCCCTTCCCGCCAGGCCAGCCCCTCACCGCCAGGGCTCTCCAGGATGTAGTGGCTGGAGACGAAGGAGGGGCCACTGGCTTCAGGCAACCGCATGCACAGGGCCTGGCACTGGCGGGTGTTAGATTTCCGCACGAGGAACGTCTGCAAGTGGATAGGGCTCAGGCAGCTCAGGACCTTGGCGTCCCATCCCTCTCCCTCCCACCCCTGGCTGGCCAGTCCCTGGAGTGTGGGGCAAGACTCACCCCCGGGGGCTCGGTCC... | GGAGACGCCTGAGAGAGGAGGGAAGTGAGGTGCTTCTCTGGGGAACCTCCCTGCTTCCAGCCCCTTCCCGCCAGGCCAGCCCCTCACCGCCAGGGCTCTCCAGGATGTAGTGGCTGGAGACGAAGGAGGGGCCACTGGCTTCAGGCAACCGCATGCACAGGGCCTGGCACTGGCGGGTGTTAGATTTCCGCACGAGGAACGTCTGCAAGTGGATAGGGCTCAGGCAGCTCAGGACCTTGGCGTCCCATCCCTCTCCCTCCCACCCCTGGCTGGCCAGTCCCTGGAGTGTGGGGCAAGACTCACCCCCGGGGGCTCGGTCC... |
Task1_train_41368 | Located on Chromosome 11, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TGAGCCTTGTGTCCATCCTGTAGCCAAGGATGGTGGTTTCTCAGACTGACTGAGCCAGGTTACATGCCCACCCCTGGAGCTGGGGGAAGGGAGATCCCCCACCCCACCCTCCCACCCACAAAAGGAGGATTGAGGTCTTGTTACCAGAGGAAGATCTGGGGCCAGCAGAAGCCATAGAATAGACAGATGATTAAGGCCTCTCCGGCTCTAACATGTGATGCTTCCAAGGCCAGCTGCCTGACAGGTCAGAGGCTGAGGACAGGCTCTGGAGAAAGAGGGAGGTGCTGCTGGAACTGGGCCTTAAAGGACACAGTAGCTTC... | TGAGCCTTGTGTCCATCCTGTAGCCAAGGATGGTGGTTTCTCAGACTGACTGAGCCAGGTTACATGCCCACCCCTGGAGCTGGGGGAAGGGAGATCCCCCACCCCACCCTCCCACCCACAAAAGGAGGATTGAGGTCTTGTTACCAGAGGAAGATCTGGGGCCAGCAGAAGCCATAGAATAGACAGATGATTAAGGCCTCTCCGGCTCTAACATGTGATGCTTCCAAGGCCAGCTGCCTGACAGGTCAGAGGCTGAGGACAGGCTCTGGAGAAAGAGGGAGGTGCTGCTGGAACTGGGCCTTAAAGGACACAGTAGCTTC... |
Task1_train_41369 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | CCTCCCAAAGTGCTGGGATTACAGGCGTGAGACACCACGCCCAACCAAATTTTTTGTATTTTTAGTAGAAACGGGGTTTCACAGTGCTAGCCAGGATGGTCTTGATCTACTGACCTCATGATCCGCCCACCTCGTCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCCGCCCGGCCCGAGTGTTTGTTTTAATATTCTTTACGGTATACATACTGTATCTTGTATGTGTAAGAAATGTTTTATTTTATTTATTTATTATTTTTTTGAGATGGAGTCTCACTTTGTCACCCACGCTGGAGTGCAATGGTGCAATCTT... | CCTCCCAAAGTGCTGGGATTACAGGCGTGAGACACCACGCCCAACCAAATTTTTTGTATTTTTAGTAGAAACGGGGTTTCACAGTGCTAGCCAGGATGGTCTTGATCTACTGACCTCATGATCCGCCCACCTCGTCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCCGCCCGGCCCGAGTGTTTGTTTTAATATTCTTTACGGTATACATACTGTATCTTGTATGTGTAAGAAATGTTTTATTTTATTTATTTATTATTTTTTTGAGATGGAGTCTCACTTTGTCACCCACGCTGGAGTGCAATGGTGCAATCTT... |
Task1_train_41370 | This variant lies on Chromosome 11. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AGGCCTCCCAGGCTCCCCACCTGTGAGCAACATGAGCCAGGGAAGCAGGAGGAGGGCAGCCATGTGGAGGGGCGTGTGGGCTCGCAGCAGGGCCGACAGTGCAGGGCCCAGCAGCACAGAGACGTGGAGCAGGACGCCGGCGGCATGAAGCAGCAGGCACAGGAAGGGCCGGTAGTTGCCGAAGCCCACGCAGCGGCCCAGCAGGCGGCAGTGGTGGTCCCGACGCAGGATGCAGACGCGGCAGGCAGAGCAGTGTCCGCTGCGTGGCGGCACCTGGCTTTGGCATTGGTAGCAGTAACTGCAGGAAGGAACCACAGCGT... | AGGCCTCCCAGGCTCCCCACCTGTGAGCAACATGAGCCAGGGAAGCAGGAGGAGGGCAGCCATGTGGAGGGGCGTGTGGGCTCGCAGCAGGGCCGACAGTGCAGGGCCCAGCAGCACAGAGACGTGGAGCAGGACGCCGGCGGCATGAAGCAGCAGGCACAGGAAGGGCCGGTAGTTGCCGAAGCCCACGCAGCGGCCCAGCAGGCGGCAGTGGTGGTCCCGACGCAGGATGCAGACGCGGCAGGCAGAGCAGTGTCCGCTGCGTGGCGGCACCTGGCTTTGGCATTGGTAGCAGTAACTGCAGGAAGGAACCACAGCGT... |
Task1_train_41371 | A mutation on Chromosome 11 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CCACTGGGTGACCGGAGCCGGCATCTCTTTGAGCAGGAAAGGAGGAGATGCTGAGCCAGCGCGACTACGATTCGGCTTTGCTACAGGAGGTGCGGGCGTTGCTGCGGCGCCACGAGGCCTTTGAGAGCGACCTGGCGGCGCACCAGGACCGCGTGGAGCACATTGCCGCGCTGGCCCAGGAGCTCAAGTAGGCGGGGCCTCGCGGGGCCCGCCCCCAACACCCCCGGCCCCGCCCCCGGTGGCGAGCCCCACCCTGATCCCCATTGCCCTTCTCAAGACACTAGGCTCTCCTGGGTTCTGTAACCCCGCCGTGGTACCCA... | CCACTGGGTGACCGGAGCCGGCATCTCTTTGAGCAGGAAAGGAGGAGATGCTGAGCCAGCGCGACTACGATTCGGCTTTGCTACAGGAGGTGCGGGCGTTGCTGCGGCGCCACGAGGCCTTTGAGAGCGACCTGGCGGCGCACCAGGACCGCGTGGAGCACATTGCCGCGCTGGCCCAGGAGCTCAAGTAGGCGGGGCCTCGCGGGGCCCGCCCCCAACACCCCCGGCCCCGCCCCCGGTGGCGAGCCCCACCCTGATCCCCATTGCCCTTCTCAAGACACTAGGCTCTCCTGGGTTCTGTAACCCCGCCGTGGTACCCA... |
Task1_train_41372 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | GAGTTTGCCCGGCGGGCCGCGCCCTTCAACAACTGGCTGGATGGTGCCGTGGAGGACCTGCAGGACGTGTGGCTGGTACACTCTGTGGAGGAGACCCAGGTGGGTGCCAGGGTTGCAGGGGATGGATAGGATGACAGGAAAGCTGGCCCCAAATTCTGCCACCCACAACTTTAGGCTCCTGGGGCATAGGGATGGGAGGAAAACCCCAGTTCCCGAGTGCTGGGCTGGAAGACAGGAGGCCGGGGTTCTTGTGTCAGGACTGCCCAGGACTGGTGGGTGGCCTGGGGCACACTGCTGCCCTTTCTGTTGCCTGTGGTAAG... | GAGTTTGCCCGGCGGGCCGCGCCCTTCAACAACTGGCTGGATGGTGCCGTGGAGGACCTGCAGGACGTGTGGCTGGTACACTCTGTGGAGGAGACCCAGGTGGGTGCCAGGGTTGCAGGGGATGGATAGGATGACAGGAAAGCTGGCCCCAAATTCTGCCACCCACAACTTTAGGCTCCTGGGGCATAGGGATGGGAGGAAAACCCCAGTTCCCGAGTGCTGGGCTGGAAGACAGGAGGCCGGGGTTCTTGTGTCAGGACTGCCCAGGACTGGTGGGTGGCCTGGGGCACACTGCTGCCCTTTCTGTTGCCTGTGGTAAG... |
Task1_train_41373 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AGGGATGGCTAGGGAATATCCCGGGGCCCCAGGGAGCCTCACCTCGTGACAATCTTGCAGGAAATGCTGCTGCTCCCGGTTGTCCCGAAGACGGCCCAGAAATTGCTGCGCTGCGTCTTGATTCTTCTTGTGCCTGGAACGACACCCTCTTGTGAAACTCTGGAATTTGCTGTGAAAGGATTGTGACCCTTTGGCTAACCTAGGGGCCTCCATTTCTTCTAGGGGAATAACGCCTTCCGGGAGCACAATGAGGCTACCCAGGAATCCTGACTTCCTTTTAGCCCTGGTTGGGGGTGGAATCTCCCAGCCCTCTCCAACCA... | AGGGATGGCTAGGGAATATCCCGGGGCCCCAGGGAGCCTCACCTCGTGACAATCTTGCAGGAAATGCTGCTGCTCCCGGTTGTCCCGAAGACGGCCCAGAAATTGCTGCGCTGCGTCTTGATTCTTCTTGTGCCTGGAACGACACCCTCTTGTGAAACTCTGGAATTTGCTGTGAAAGGATTGTGACCCTTTGGCTAACCTAGGGGCCTCCATTTCTTCTAGGGGAATAACGCCTTCCGGGAGCACAATGAGGCTACCCAGGAATCCTGACTTCCTTTTAGCCCTGGTTGGGGGTGGAATCTCCCAGCCCTCTCCAACCA... |
Task1_train_41374 | This variant is found on Chromosome 11. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GCCCGTCTCCGGGAGATGGTGAAGGGGCCCGCGAGCAGGCGCTTTGTCTGGCTGTCTGCAGAGTGAGGTTCGCGCCGCGGCGGCGGGCGCCCGTGCGGTGCAGGATGCCGGGGCGCCAGGATGGCCGGGGGCGCGCGCGCCTGTGCCAGGGTGAGTGCGCTGCGGCAGCGCCGGGGGACAGCGCGGAGGGCCCGCGCCGGCCCGGGCCTCGGGCGTGACTGGGCGCCACCCGTGGGCGCTGCAGCGGCCGCGTGTCCCCGTGACCTCAGGAGCCGGCCCGGGCCCGGGTGGATCCCCGCGCGCCCCTCCCCGTCCGCCCT... | GCCCGTCTCCGGGAGATGGTGAAGGGGCCCGCGAGCAGGCGCTTTGTCTGGCTGTCTGCAGAGTGAGGTTCGCGCCGCGGCGGCGGGCGCCCGTGCGGTGCAGGATGCCGGGGCGCCAGGATGGCCGGGGGCGCGCGCGCCTGTGCCAGGGTGAGTGCGCTGCGGCAGCGCCGGGGGACAGCGCGGAGGGCCCGCGCCGGCCCGGGCCTCGGGCGTGACTGGGCGCCACCCGTGGGCGCTGCAGCGGCCGCGTGTCCCCGTGACCTCAGGAGCCGGCCCGGGCCCGGGTGGATCCCCGCGCGCCCCTCCCCGTCCGCCCT... |
Task1_train_41375 | A variant was discovered on Chromosome 11. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CAAAAAAAAAAAAAAAATTATGGTAATGAAGGCATGGAAGATGCTTATGGAATAAAAGGTTCTTGTTTTCTCAAATCCCAAGGTCAATTTAGGGAAAATAAAACTATTTATTTATTTATTTATTTATTTATTTATTTATTTTTGAGACAGAGTCTCACCCTGTCGCCCAGTCTGGAGTGCAGCGGCGCAATCTCAGCTCACTGCAACCTCCGCCTCCTGGATTCAAGCAGTTCTCCTGCCTCAGCCTCCTGAGTAGCTGAGATTATAGGTGCATGCCGCCACACCCGGCTAATTTTTGTAGTTTTAGTAGAGACGGTTTC... | CAAAAAAAAAAAAAAAATTATGGTAATGAAGGCATGGAAGATGCTTATGGAATAAAAGGTTCTTGTTTTCTCAAATCCCAAGGTCAATTTAGGGAAAATAAAACTATTTATTTATTTATTTATTTATTTATTTATTTATTTTTGAGACAGAGTCTCACCCTGTCGCCCAGTCTGGAGTGCAGCGGCGCAATCTCAGCTCACTGCAACCTCCGCCTCCTGGATTCAAGCAGTTCTCCTGCCTCAGCCTCCTGAGTAGCTGAGATTATAGGTGCATGCCGCCACACCCGGCTAATTTTTGTAGTTTTAGTAGAGACGGTTTC... |
Task1_train_41376 | A mutation on Chromosome 11 is under examination. Does this mutation cause a disorder, or is it a benign change? | Benign | GATTCATGCTAATTCCTCAGTGTCTTCTAGTCCCAAGTCCATGCTCAAGTGTCCCCCCCTGTCCAGGCACCCTCTTCAGGGGTCCTCCATGTTTCATAGCGAGAAGGGGCCCTGAGAGTTGGGCACCCCGGGCAGGCTGGCTGGAGGGGGCTTTGGAAAGGAAGGCTTTGGCCAGCGTGTGAGGGTGCAGGTCTCACCAGCTCCTGTTTGGTCTGTTTCAGGAACAAATGTGGTATCTGGGGCTGGCGGTCTGAGAAGATGGAAACTGTTAGCGGCTACGAGGCCAAGGCAGGAGAGGCTAGGGGTGGGGGGCTGGGGGT... | GATTCATGCTAATTCCTCAGTGTCTTCTAGTCCCAAGTCCATGCTCAAGTGTCCCCCCCTGTCCAGGCACCCTCTTCAGGGGTCCTCCATGTTTCATAGCGAGAAGGGGCCCTGAGAGTTGGGCACCCCGGGCAGGCTGGCTGGAGGGGGCTTTGGAAAGGAAGGCTTTGGCCAGCGTGTGAGGGTGCAGGTCTCACCAGCTCCTGTTTGGTCTGTTTCAGGAACAAATGTGGTATCTGGGGCTGGCGGTCTGAGAAGATGGAAACTGTTAGCGGCTACGAGGCCAAGGCAGGAGAGGCTAGGGGTGGGGGGCTGGGGGT... |
Task1_train_41377 | A variant has been detected on Chromosome 11. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | TTCAATTCTGGCGGGGGTGGGGATGGGTGGCGACAGTAACCAAATTCACAAGATATTTATAGATTGTCAGAAGTGTCATGAAGAAAATAAAACAAGGGATGTGACAGGGAGTGTCAGGGGAGTGCAGGGGCGATGGCTGCATTTAAGCTCCTTCTGGCTGCTCTGTGCAGGAGGAGGACTCACAGGGGTGGCTGTGGAGGCCTGGGGCCAGAGAGGCCACTGTCCCCAGGGGCCAGGCTACAGTCTACGAAGCAGGGAGGGCTTGGAGCCATGAAGCCAGAGAGGTGGAGGCTGGGGGCCAGGCCAAGAACAGGAGGGGA... | TTCAATTCTGGCGGGGGTGGGGATGGGTGGCGACAGTAACCAAATTCACAAGATATTTATAGATTGTCAGAAGTGTCATGAAGAAAATAAAACAAGGGATGTGACAGGGAGTGTCAGGGGAGTGCAGGGGCGATGGCTGCATTTAAGCTCCTTCTGGCTGCTCTGTGCAGGAGGAGGACTCACAGGGGTGGCTGTGGAGGCCTGGGGCCAGAGAGGCCACTGTCCCCAGGGGCCAGGCTACAGTCTACGAAGCAGGGAGGGCTTGGAGCCATGAAGCCAGAGAGGTGGAGGCTGGGGGCCAGGCCAAGAACAGGAGGGGA... |
Task1_train_41378 | With a mutation on Chromosome 11, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CTTCCTGGAAGATACGGCCTGGTGGGTGTTAATCCTCCGCTTTCCTGAGGCTGCCAGGTCCCTGCTCTACTCCCGCCTTCACCCTGTCTTGTTTCTGCAGCTTCTACCTGGCTGAGATCACGCTGGCCCTGGGCCATCTCCACTCCCAGGGCATCATCTACCGGGACCTCAAGCCCGAGAACATCATGCTCAGCAGCCAGGGTGCGCATGTGTGTGCGGGCAGCTGCAGGCGGGGTCTGCAATCTGTGGGGAGGGCTGAGGACCTCTGTGGGTGGGGTGGGGCCCTGGTCACGCCTCTCCAACACCCTTCCTCAGGCCAC... | CTTCCTGGAAGATACGGCCTGGTGGGTGTTAATCCTCCGCTTTCCTGAGGCTGCCAGGTCCCTGCTCTACTCCCGCCTTCACCCTGTCTTGTTTCTGCAGCTTCTACCTGGCTGAGATCACGCTGGCCCTGGGCCATCTCCACTCCCAGGGCATCATCTACCGGGACCTCAAGCCCGAGAACATCATGCTCAGCAGCCAGGGTGCGCATGTGTGTGCGGGCAGCTGCAGGCGGGGTCTGCAATCTGTGGGGAGGGCTGAGGACCTCTGTGGGTGGGGTGGGGCCCTGGTCACGCCTCTCCAACACCCTTCCTCAGGCCAC... |
Task1_train_41379 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | AGCATCAGCAGCTTGAGAGGGAAGAGCTGGTTCTGCCCTAGAGAAGCTGTGTGACCTCTGGGAGCCTTTGCCCTTTCTAATTTTTTTTTTTTTTTTTGAGATGGAGTCTTGCTCTGTCGCCAGGCTGGAGTGCAGTGGTACAATCCCGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGTGTGCGCCGCTACGCCCAGCTAATTTTTGTACTTTTAATAGAGACGGGGTTTCACCATGTTGGCCAGGATGGTCTTGATCTTTTGACCTTGTGATCCG... | AGCATCAGCAGCTTGAGAGGGAAGAGCTGGTTCTGCCCTAGAGAAGCTGTGTGACCTCTGGGAGCCTTTGCCCTTTCTAATTTTTTTTTTTTTTTTTGAGATGGAGTCTTGCTCTGTCGCCAGGCTGGAGTGCAGTGGTACAATCCCGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGTGTGCGCCGCTACGCCCAGCTAATTTTTGTACTTTTAATAGAGACGGGGTTTCACCATGTTGGCCAGGATGGTCTTGATCTTTTGACCTTGTGATCCG... |
Task1_train_41380 | This variant is present on Chromosome 11. Is the change likely to result in a pathogenic outcome? | Benign | CTCAGGAAATGCCCGCTGATGGCAGCCCGGCAGTCAGCCCCTGTCCAGACAACAGGGCAGTGGGAGGAGTGGGGAGGACCCGGGTAGGAGGAATCTGGTTATCTGGTTCCCACCAGCCTAGCAGCTTTGCCAAGCAAGAGATTAGAGGCTAGGTCCCCTATGCCTGTCTCCCTGTGGGGTTTTTTTTTTTTTGACTAAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCGTGATCTTGGCTCACTGCAACCACCATCTCCTGGGTTCAGCTGATTCTCTGCCTTAGCTGCCTGAGTAGCTGGGATTACAGGCACCT... | CTCAGGAAATGCCCGCTGATGGCAGCCCGGCAGTCAGCCCCTGTCCAGACAACAGGGCAGTGGGAGGAGTGGGGAGGACCCGGGTAGGAGGAATCTGGTTATCTGGTTCCCACCAGCCTAGCAGCTTTGCCAAGCAAGAGATTAGAGGCTAGGTCCCCTATGCCTGTCTCCCTGTGGGGTTTTTTTTTTTTTGACTAAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCGTGATCTTGGCTCACTGCAACCACCATCTCCTGGGTTCAGCTGATTCTCTGCCTTAGCTGCCTGAGTAGCTGGGATTACAGGCACCT... |
Task1_train_41381 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | CATGCTGGTGGGCAGAGGCTGTGGTCCTTGAGTCCTTTATGCTGCCTCCAGCTTCTGTACAGGCTCACCGAGACATCATTCGCACAAACTCTGCCAGGACGAAGCCAAGGTTTTGGGTCTGTTCTCTGGACTGCGCTAGGAGTGAGGATCATCTGCAGGCCTTGGGGCGGGTGGGAGTGTGGTTGAGGGGAGGGTCTTCAAGGGCATCCTCTGGATCTGATAGGGAATAGGCCTCAGAGCCGGGAAGAGGAGGCTTTGTCTTATGGGGGAAAAACAAACAAACCCTTGTAATGGAACTTGTTTTCCTTTTTGCTTTGACA... | CATGCTGGTGGGCAGAGGCTGTGGTCCTTGAGTCCTTTATGCTGCCTCCAGCTTCTGTACAGGCTCACCGAGACATCATTCGCACAAACTCTGCCAGGACGAAGCCAAGGTTTTGGGTCTGTTCTCTGGACTGCGCTAGGAGTGAGGATCATCTGCAGGCCTTGGGGCGGGTGGGAGTGTGGTTGAGGGGAGGGTCTTCAAGGGCATCCTCTGGATCTGATAGGGAATAGGCCTCAGAGCCGGGAAGAGGAGGCTTTGTCTTATGGGGGAAAAACAAACAAACCCTTGTAATGGAACTTGTTTTCCTTTTTGCTTTGACA... |
Task1_train_41382 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | GGGGGGCAGACTGCGCTCACCGCGCCTTGGCATCCTCCCCCGGGCTCCAGCAAACTTTTCTTTGTTCGCTGCAGTGCCGCCCTACACCGTGGTCTATTTCCCAGTTCGAGGTAGGAGCATGTGTCTGGCAGGGAAGGGAGGCAGGGGCTGGGGCTGCAGCCCACAGCCCCTCGCCCACCCGGAGAGATCCGAACCCCCTTATCCCTCCGTCGTGTGGCTTTTACCCCGGGCCTCCTTCCTGTTCCCCGCCTCTCCCGCCATGCCTGCTCCCCGCCCCAGTGTTGTGTGAAATCTTCGGAGGAACCTGTTTCCCTGTTCCC... | GGGGGGCAGACTGCGCTCACCGCGCCTTGGCATCCTCCCCCGGGCTCCAGCAAACTTTTCTTTGTTCGCTGCAGTGCCGCCCTACACCGTGGTCTATTTCCCAGTTCGAGGTAGGAGCATGTGTCTGGCAGGGAAGGGAGGCAGGGGCTGGGGCTGCAGCCCACAGCCCCTCGCCCACCCGGAGAGATCCGAACCCCCTTATCCCTCCGTCGTGTGGCTTTTACCCCGGGCCTCCTTCCTGTTCCCCGCCTCTCCCGCCATGCCTGCTCCCCGCCCCAGTGTTGTGTGAAATCTTCGGAGGAACCTGTTTCCCTGTTCCC... |
Task1_train_41383 | Given a variant located on Chromosome 11, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TGTATCTAGCTACTCTGGTGGGGCCTTGGAGAACCTTTATGTCTAGCTCAGGGATTGTAAATACACCAATCGGCACTCTGTATCTAACTCAAGGTTTGTAAATACACCAATCAGCACCCTGTGTCTAGCTCAGGGTTTGTGAATGCACCAACGGACACTCTGTATCTAGCTACCCTGGTGGGGACTTGGAGAACCGTTGTGTCGACACTCTGTATCTAACTAATCTGGTGGGGACTTGGAGAACCTTTGTGTCTAGCTCAGGGATTGTAAACGCACCAATCAGCGCCCTGTCAAAACAAACCACTTGTCTCTACCAATCA... | TGTATCTAGCTACTCTGGTGGGGCCTTGGAGAACCTTTATGTCTAGCTCAGGGATTGTAAATACACCAATCGGCACTCTGTATCTAACTCAAGGTTTGTAAATACACCAATCAGCACCCTGTGTCTAGCTCAGGGTTTGTGAATGCACCAACGGACACTCTGTATCTAGCTACCCTGGTGGGGACTTGGAGAACCGTTGTGTCGACACTCTGTATCTAACTAATCTGGTGGGGACTTGGAGAACCTTTGTGTCTAGCTCAGGGATTGTAAACGCACCAATCAGCGCCCTGTCAAAACAAACCACTTGTCTCTACCAATCA... |
Task1_train_41384 | An alteration has been detected on Chromosome 11. Is it pathogenic, and if so, what disease is involved? | Benign | TGGGAGGGCAGTAGTCTGTGCCAGTGAGGGCTGCAAGCCTCAGGGCTCAGTCTCCACCCCTGTGAAATGGGCCTGCAGCGGGTGCTCCCGAGCTGGTTCACCCACCCTGTGGTTCTGATAGGCTGTCACTGCTGTGAACTGGGTCTCTGTGAAGATGAAGGACTTGAAGTTCTCCTGGGCATAGCGCTCACTGTCCTTGCGTGGGTCCACGAAGACCACGTGGAAACGGGGCTGGTAGCGGTGCATAGAGTTGAGAATGATCTGTGGAAGGGACAGAGCAGGGGTACAGGGGTGAGGCGGAGTACAGCGGACTCCCTGAG... | TGGGAGGGCAGTAGTCTGTGCCAGTGAGGGCTGCAAGCCTCAGGGCTCAGTCTCCACCCCTGTGAAATGGGCCTGCAGCGGGTGCTCCCGAGCTGGTTCACCCACCCTGTGGTTCTGATAGGCTGTCACTGCTGTGAACTGGGTCTCTGTGAAGATGAAGGACTTGAAGTTCTCCTGGGCATAGCGCTCACTGTCCTTGCGTGGGTCCACGAAGACCACGTGGAAACGGGGCTGGTAGCGGTGCATAGAGTTGAGAATGATCTGTGGAAGGGACAGAGCAGGGGTACAGGGGTGAGGCGGAGTACAGCGGACTCCCTGAG... |
Task1_train_41385 | A mutation is present on Chromosome 11. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GCAGCACAGGGTCTGAGCTGGAGAGGCTGCAGTTCCGTGTCAAAGGCCCCTTTGGATCATGGATCCTTGCCTCCATGTCCTCTCACACCCCACATCCCAGCTGCCACCCACTGCCTGTGTGCTGGCCCGTCACTGTCGCGTTCACCAGTTTCCTCGGTTGCCTCCTGGCCTGTCCCCTGTCCCCGCCTTACCCCTCTGTTCCTTCTCCACACAGCTGCCCGGGAAGCCACATCATATGCCCCCTGCTCCTAACCGTCCAGCGACTTCCACCCCACACGGTAAAAGCCAGAGCCCCCCGAAGTCAGCCCGACCCCTCAGGC... | GCAGCACAGGGTCTGAGCTGGAGAGGCTGCAGTTCCGTGTCAAAGGCCCCTTTGGATCATGGATCCTTGCCTCCATGTCCTCTCACACCCCACATCCCAGCTGCCACCCACTGCCTGTGTGCTGGCCCGTCACTGTCGCGTTCACCAGTTTCCTCGGTTGCCTCCTGGCCTGTCCCCTGTCCCCGCCTTACCCCTCTGTTCCTTCTCCACACAGCTGCCCGGGAAGCCACATCATATGCCCCCTGCTCCTAACCGTCCAGCGACTTCCACCCCACACGGTAAAAGCCAGAGCCCCCCGAAGTCAGCCCGACCCCTCAGGC... |
Task1_train_41386 | A change on Chromosome 11 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | CTGGCTCCCCAACCCCTGAGCCAGACCTGCTCTTCCCCGGACCTGTTTCCCGAAAGTCCCCTGGGGTCTCACCCTGGTTGAAGAGTTCGATGAAGTCCAGAACTGTGGCCACCAGGGTCCTCATCCTTGAGAAAATGTCAGCCCGCAGCACACCCTGTGGCTGGGGGCCCAGCTCCAGACCTGGGGACCAGGAAGCAAGGGGTTAGGCAGGTGCAGGACCCATATACTCCTTGAAGAGGCCCTGCCCCTTGGTGACTGGACCCGCCCCTCCAGCCCTCCTGGCCCCGCCCACTTCTCAGAAGGCTGCGGCCCACCCAGTC... | CTGGCTCCCCAACCCCTGAGCCAGACCTGCTCTTCCCCGGACCTGTTTCCCGAAAGTCCCCTGGGGTCTCACCCTGGTTGAAGAGTTCGATGAAGTCCAGAACTGTGGCCACCAGGGTCCTCATCCTTGAGAAAATGTCAGCCCGCAGCACACCCTGTGGCTGGGGGCCCAGCTCCAGACCTGGGGACCAGGAAGCAAGGGGTTAGGCAGGTGCAGGACCCATATACTCCTTGAAGAGGCCCTGCCCCTTGGTGACTGGACCCGCCCCTCCAGCCCTCCTGGCCCCGCCCACTTCTCAGAAGGCTGCGGCCCACCCAGTC... |
Task1_train_41387 | A variant on Chromosome 11 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | CCCCTGCTTTGAGTTGTCCCATCTTTCTGGACCAAACCAACATATATCTTGCACGTATTGATTGATGCGTCACGTCTCCCTAAAATGTATAAATCCAAGCTGTGACCTGACAGTCTTGGGTACATGTTCTCAGGATCTCCTAAGGGCTGTGTCACGGGCCGTGGTCATTCATCTTTGGCTCAGAATAAGTCTCTTAAATATTGTACAGAGTTTGACTCTTTTGATCGACATTTGCAATAACTCGATCAAGGGTCCTTTGTGAACAAAGGTGGAACTTATTCATTTTTTCTCCCTACTTGATTCCTACAAAATTCAGAAAC... | CCCCTGCTTTGAGTTGTCCCATCTTTCTGGACCAAACCAACATATATCTTGCACGTATTGATTGATGCGTCACGTCTCCCTAAAATGTATAAATCCAAGCTGTGACCTGACAGTCTTGGGTACATGTTCTCAGGATCTCCTAAGGGCTGTGTCACGGGCCGTGGTCATTCATCTTTGGCTCAGAATAAGTCTCTTAAATATTGTACAGAGTTTGACTCTTTTGATCGACATTTGCAATAACTCGATCAAGGGTCCTTTGTGAACAAAGGTGGAACTTATTCATTTTTTCTCCCTACTTGATTCCTACAAAATTCAGAAAC... |
Task1_train_41388 | Here’s a variant located on Chromosome 11. What is the predicted biological effect — harmless or disease-causing? | Benign | ATGCGTCACGTCTCCCTAAAATGTATAAATCCAAGCTGTGACCTGACAGTCTTGGGTACATGTTCTCAGGATCTCCTAAGGGCTGTGTCACGGGCCGTGGTCATTCATCTTTGGCTCAGAATAAGTCTCTTAAATATTGTACAGAGTTTGACTCTTTTGATCGACATTTGCAATAACTCGATCAAGGGTCCTTTGTGAACAAAGGTGGAACTTATTCATTTTTTCTCCCTACTTGATTCCTACAAAATTCAGAAACTATTCATGAACATTCTTATTTATATATAGTAAAACAAACAAACAAAAACAAACAAACAAAAACC... | ATGCGTCACGTCTCCCTAAAATGTATAAATCCAAGCTGTGACCTGACAGTCTTGGGTACATGTTCTCAGGATCTCCTAAGGGCTGTGTCACGGGCCGTGGTCATTCATCTTTGGCTCAGAATAAGTCTCTTAAATATTGTACAGAGTTTGACTCTTTTGATCGACATTTGCAATAACTCGATCAAGGGTCCTTTGTGAACAAAGGTGGAACTTATTCATTTTTTCTCCCTACTTGATTCCTACAAAATTCAGAAACTATTCATGAACATTCTTATTTATATATAGTAAAACAAACAAACAAAAACAAACAAACAAAAACC... |
Task1_train_41389 | Here is a mutation located on Chromosome 11. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GGAATACTACAGTCTTGAGGACGTGCTTTCCATACGCCCTGTGTCTGGTCTACATGCAGGCGTGTCTTGTGATAAATCCTGTTACGGGCATGTGTGTGTGAGGGCTTCTATGTGGCCCCCCGACTCCATTTTATTAGAGTTTGGCATAAGTGACTCCATTTTGGTTCCAGCAACTTTCACATAAGGAAACTGAGGCTCAGAGAAGTCAAGGGACTTGCCCCCAGGTCCCACTAACACTGTGCAGTGGAGTGATGCAAACCCCAGTTTTCCCAGTGGATGGAGCTGCTGTGGGTGAGTGCAGGGTGCGGTGTGAACCAGAG... | GGAATACTACAGTCTTGAGGACGTGCTTTCCATACGCCCTGTGTCTGGTCTACATGCAGGCGTGTCTTGTGATAAATCCTGTTACGGGCATGTGTGTGTGAGGGCTTCTATGTGGCCCCCCGACTCCATTTTATTAGAGTTTGGCATAAGTGACTCCATTTTGGTTCCAGCAACTTTCACATAAGGAAACTGAGGCTCAGAGAAGTCAAGGGACTTGCCCCCAGGTCCCACTAACACTGTGCAGTGGAGTGATGCAAACCCCAGTTTTCCCAGTGGATGGAGCTGCTGTGGGTGAGTGCAGGGTGCGGTGTGAACCAGAG... |
Task1_train_41390 | Here is a genetic alteration on Chromosome 11. Based on the data, is it a benign variant or a cause of disease? | Benign | GGTGCGGTGGTGGGAGAAGGTGTCGAAGGTGAACTTGCCGTGGTACCGGCCCATCCCACTGTGGCCTGTGTGGGCACAGAGAACAAGGGCCTGAGACCAGGCAGCCCATGGAGCCCCAGCAGCAGCCCACTGCCCCGGCCAGGGCACACAGCTGGCAGGGAGCTCAGAGAGAGCCAGGCCACTCACAGAGCCATTTTACAGATAGGGAAACTGAGGCCTTGAGAGGCCCAGGGTGTGGATCAAGGTTGAACAGTGAGTGAAGGGACTTCCTGGGTCTGGGGTACCAAAGCCAAGCTTCCCTAGGGGTGGAAATGGGCAGG... | GGTGCGGTGGTGGGAGAAGGTGTCGAAGGTGAACTTGCCGTGGTACCGGCCCATCCCACTGTGGCCTGTGTGGGCACAGAGAACAAGGGCCTGAGACCAGGCAGCCCATGGAGCCCCAGCAGCAGCCCACTGCCCCGGCCAGGGCACACAGCTGGCAGGGAGCTCAGAGAGAGCCAGGCCACTCACAGAGCCATTTTACAGATAGGGAAACTGAGGCCTTGAGAGGCCCAGGGTGTGGATCAAGGTTGAACAGTGAGTGAAGGGACTTCCTGGGTCTGGGGTACCAAAGCCAAGCTTCCCTAGGGGTGGAAATGGGCAGG... |
Task1_train_41391 | Consider a variant on Chromosome 11. Determine its clinical classification and disease relevance. | Benign | GGTATCCTGGTCTTTGGCAGAGTCCACGTAAAAGAAGGAGGTAGAGGGAGTGAGAGGGACTTCATGCAATAAAGTTTCCCGGCGTTACACTGCCATCGTAATTGTGTCCCCGACCAGGACCTCTCCCTTCTCATCCTTTCCGTGATCGGCCCTGGAAAACCTTCCAGAGAACTGTCCTCCTTCTCCCAGGATCTCAGAGAAAATTCGCCTGAGTTCAGTGTCCAGGTGACCCAAGCTCTGAATGCGGTAACGTGCACGGGGAGATAAGGATGTCACCATGAGCAAGCCTCCCAGACGGCATCCAGGAGCAACCCCAAGAC... | GGTATCCTGGTCTTTGGCAGAGTCCACGTAAAAGAAGGAGGTAGAGGGAGTGAGAGGGACTTCATGCAATAAAGTTTCCCGGCGTTACACTGCCATCGTAATTGTGTCCCCGACCAGGACCTCTCCCTTCTCATCCTTTCCGTGATCGGCCCTGGAAAACCTTCCAGAGAACTGTCCTCCTTCTCCCAGGATCTCAGAGAAAATTCGCCTGAGTTCAGTGTCCAGGTGACCCAAGCTCTGAATGCGGTAACGTGCACGGGGAGATAAGGATGTCACCATGAGCAAGCCTCCCAGACGGCATCCAGGAGCAACCCCAAGAC... |
Task1_train_41392 | Chromosome 11 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | GTGGGTCTCGTGCTTACCCGTGGGGGCCAGGCCTGCCAGCACGGGAACAATATGACTCGGTCAGAGCTCTGGTCAGACCCCTGTGTGTGCCTGGCAGGAGCCCCGGCAGCCGCCGCCGCTACTTTCTGTGTGCACAGCAACCCCTCCCAGTGTTCTGTGACTCGGGTGGCTCCTGTCCAGATCCTAGTTTGTCCTCTGGAGCACTCCCAGGTCCTCCAGGCCATGAGCTGCGGCCCTGATGTCTCTACTCCAGCCACGGACTGAGAGTGCATAGGAGTGTCCCCAAACAGCAGTCACGATGGTCACAACCTTGGCTTCCA... | GTGGGTCTCGTGCTTACCCGTGGGGGCCAGGCCTGCCAGCACGGGAACAATATGACTCGGTCAGAGCTCTGGTCAGACCCCTGTGTGTGCCTGGCAGGAGCCCCGGCAGCCGCCGCCGCTACTTTCTGTGTGCACAGCAACCCCTCCCAGTGTTCTGTGACTCGGGTGGCTCCTGTCCAGATCCTAGTTTGTCCTCTGGAGCACTCCCAGGTCCTCCAGGCCATGAGCTGCGGCCCTGATGTCTCTACTCCAGCCACGGACTGAGAGTGCATAGGAGTGTCCCCAAACAGCAGTCACGATGGTCACAACCTTGGCTTCCA... |
Task1_train_41393 | This alteration on Chromosome 11 may affect genome function. Does it lead to a disease or is it benign? | Benign | GGAGTGGCACTGCGAGGCACAGCGGCACGAGGGTGACAGCAGGCCCAGGGAGGGCTCAGCAGGAGGAAAGCTGGGCTGTGTTAAACCAGGAACAGGAGGAGGTGCGAATGCAGTCACCGGAAGCAGGTCCGATGAAGAGGCCTCGAAGTCCACCCCACAGAGTCAGGACTTAACTTTGCACACAATCTGCCAACTTGGGTGGCAGAAGTTATTCCCACGCAGCAGTGCCAGGCTTGGACGAGGACTCACCCAGGTGGTAATGAGGGCCCTCCTTCGAGCTCAGGCCAGGAAGCAGCAGCCCTGACCACCGCTGCTAACCC... | GGAGTGGCACTGCGAGGCACAGCGGCACGAGGGTGACAGCAGGCCCAGGGAGGGCTCAGCAGGAGGAAAGCTGGGCTGTGTTAAACCAGGAACAGGAGGAGGTGCGAATGCAGTCACCGGAAGCAGGTCCGATGAAGAGGCCTCGAAGTCCACCCCACAGAGTCAGGACTTAACTTTGCACACAATCTGCCAACTTGGGTGGCAGAAGTTATTCCCACGCAGCAGTGCCAGGCTTGGACGAGGACTCACCCAGGTGGTAATGAGGGCCCTCCTTCGAGCTCAGGCCAGGAAGCAGCAGCCCTGACCACCGCTGCTAACCC... |
Task1_train_41394 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | GCCCTGGCCAAGAAACGGGGCCGTCAGAACGCTGCACTAACTGCAGCCTTGGGCCTCCATGCCAGAGGCCATGCCCTTCCATCCACCACCCCCTGGCCTGGGCCCTGGCCCTCCTGGCTCGGGAACTCCAGGCCCCTTCCTCACGGCTCGAGAGACGTGTATTTACCGCACAGGTGCTTGTCATTCTCTTGTGGCCTCTTCTCCAGGGAGATCACAGAAGGACAGGGCCTCACTGAGGTCTCGGACATGGACCCTTTGATAGTGGCAGGAGCCAGGCTGGGCAAGAGGCGGCCACAGTCACCTCAGCAGTGCCATCACCA... | GCCCTGGCCAAGAAACGGGGCCGTCAGAACGCTGCACTAACTGCAGCCTTGGGCCTCCATGCCAGAGGCCATGCCCTTCCATCCACCACCCCCTGGCCTGGGCCCTGGCCCTCCTGGCTCGGGAACTCCAGGCCCCTTCCTCACGGCTCGAGAGACGTGTATTTACCGCACAGGTGCTTGTCATTCTCTTGTGGCCTCTTCTCCAGGGAGATCACAGAAGGACAGGGCCTCACTGAGGTCTCGGACATGGACCCTTTGATAGTGGCAGGAGCCAGGCTGGGCAAGAGGCGGCCACAGTCACCTCAGCAGTGCCATCACCA... |
Task1_train_41395 | Chromosome 11 is altered by this variant. Does this mutation result in a disease or is it benign? | Benign | GCCACCATGCCTGGCTAATGTTTTCATTTTTTGTAGAGACAGGATCTTGCCACATTGACCAGACTGGTCTTCAACTACTGGGCTCGAGCAATCCTCCGGCCTGGCCTCACAAAGTGCTGAGATTACAGGCGTGAGCCAGCACTCCAGGCTGGTATTTTATGATTTTAAAGAAAGCCCAGGGACATCTATTGGATACCACAGGAACTACTTTTTTTTTTTTTTTTTTTTTTGAGACAGGGTCTCACTTTGTCACCCAGGCTAGAGTGCAGTAGTGCGATGTTGGCTCACTGCAGCCTCAGCCTCAACCTTCTGGCCTCAAG... | GCCACCATGCCTGGCTAATGTTTTCATTTTTTGTAGAGACAGGATCTTGCCACATTGACCAGACTGGTCTTCAACTACTGGGCTCGAGCAATCCTCCGGCCTGGCCTCACAAAGTGCTGAGATTACAGGCGTGAGCCAGCACTCCAGGCTGGTATTTTATGATTTTAAAGAAAGCCCAGGGACATCTATTGGATACCACAGGAACTACTTTTTTTTTTTTTTTTTTTTTTGAGACAGGGTCTCACTTTGTCACCCAGGCTAGAGTGCAGTAGTGCGATGTTGGCTCACTGCAGCCTCAGCCTCAACCTTCTGGCCTCAAG... |
Task1_train_41396 | This variant is located on Chromosome 11. Evaluate its biological effect and specify any disease association. | Benign | GCCGAAGCGGGCGGATCACTTGAGTCCAGGAGTTTGAGATCAGCCTGGGCAACACGGCAAAACCTCATCTCTATAAAAAATGCAAAAATTAGCCAGGCATGATGCATGTGCCTGTGGTCTCAGCTACTGGGGAGGCTAAGATGGGAGGATTCCTTGAGCTCAGGAGGTGGAGGCTGAAGTGAGCCGTGATCATGTCACTGCACTCCAGCCTGGGTGGCAGAGAGAGACCTCATGTCAAAATAAATAAATAAATAAATAAATCAAACACTCTATGAGACAGTTGGCAGTCTTCAACCAAAGAGAAATTAAAATCTGGAAAT... | GCCGAAGCGGGCGGATCACTTGAGTCCAGGAGTTTGAGATCAGCCTGGGCAACACGGCAAAACCTCATCTCTATAAAAAATGCAAAAATTAGCCAGGCATGATGCATGTGCCTGTGGTCTCAGCTACTGGGGAGGCTAAGATGGGAGGATTCCTTGAGCTCAGGAGGTGGAGGCTGAAGTGAGCCGTGATCATGTCACTGCACTCCAGCCTGGGTGGCAGAGAGAGACCTCATGTCAAAATAAATAAATAAATAAATAAATCAAACACTCTATGAGACAGTTGGCAGTCTTCAACCAAAGAGAAATTAAAATCTGGAAAT... |
Task1_train_41397 | Consider this mutation on Chromosome 11. Is this a benign change or a disease-causing variant? | Benign | TTGGGATTACAGGCATGAGCTACCGTGCCTAGCCTCCATTGAGTTTTAAAATAATGTTCTTTTTAGTGTATATAAATCTTTTATTTTGAAATGTAATGATATTTCTTTTAGCTTAGTACTTTGTGAAAATAGAGGAAAGCTGATCATACTTTATGCTTGATAGCAATTTTAGGTTGGAAAAATCTTTTTTTTTTTTTTTTGAGACGGAGACTTGCTCTGTCACCAAGAGTGGGGTGCAGTGGTGCGACCTCGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGTGACTCTCCTGCCTCAGCCTCCCAAGTAGTTGGGAT... | TTGGGATTACAGGCATGAGCTACCGTGCCTAGCCTCCATTGAGTTTTAAAATAATGTTCTTTTTAGTGTATATAAATCTTTTATTTTGAAATGTAATGATATTTCTTTTAGCTTAGTACTTTGTGAAAATAGAGGAAAGCTGATCATACTTTATGCTTGATAGCAATTTTAGGTTGGAAAAATCTTTTTTTTTTTTTTTTGAGACGGAGACTTGCTCTGTCACCAAGAGTGGGGTGCAGTGGTGCGACCTCGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGTGACTCTCCTGCCTCAGCCTCCCAAGTAGTTGGGAT... |
Task1_train_41398 | This mutation is located on Chromosome 11. Is it associated with a disease or is it a benign polymorphism? | Benign | TTTTTGGAGACGGAGCCTCACTCTGTCACCCAGGCTAGAGTCTGGAGTGCAGGGGCGGGATCTTGGCTCCCTGCAACCTCCGCCTCCCGGGTTTAAGTGATTCTCCTACCTCAGCCTCCCGAACAGCTGGGATTATAGGCGTGCGCCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGAGTTTCACCACATTGGCCAGTCTGGTCTCACTCCTGACTTCAGTTGATCTGCCTGCCTCAGCCTCCCAAAGTGCTACGATTACAGGCATGAGCCACTGTGCCCGGCCCAGTTACATTTTTAATGGCTGAAAAAG... | TTTTTGGAGACGGAGCCTCACTCTGTCACCCAGGCTAGAGTCTGGAGTGCAGGGGCGGGATCTTGGCTCCCTGCAACCTCCGCCTCCCGGGTTTAAGTGATTCTCCTACCTCAGCCTCCCGAACAGCTGGGATTATAGGCGTGCGCCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGAGTTTCACCACATTGGCCAGTCTGGTCTCACTCCTGACTTCAGTTGATCTGCCTGCCTCAGCCTCCCAAAGTGCTACGATTACAGGCATGAGCCACTGTGCCCGGCCCAGTTACATTTTTAATGGCTGAAAAAG... |
Task1_train_41399 | This alteration occurs on Chromosome 11. Is it associated with a disease or is it a benign variant? | Benign | AAAACAATTAGCCGGGTGTGGTGGCACACACCTGCAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAACTGAGATCGCACCATTGCACTCCAGCCTGGGCAATAAGAGCAAAACTCCATCTCCAAAAAAAAAAAAAAAAAAAAAAAAACCAAAAAAACCACGAGGAAACTGAGAAACAAGGTCAAATGCCCAGCACTCAGAGTGGCAGAGCCAGCAATGGAACTCGGGCAGAGCGCAGGGAAGCCTGTCACTTGCTTAAAAGATTACGTCCAGCGGTTTTCCAAT... | AAAACAATTAGCCGGGTGTGGTGGCACACACCTGCAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAACTGAGATCGCACCATTGCACTCCAGCCTGGGCAATAAGAGCAAAACTCCATCTCCAAAAAAAAAAAAAAAAAAAAAAAAACCAAAAAAACCACGAGGAAACTGAGAAACAAGGTCAAATGCCCAGCACTCAGAGTGGCAGAGCCAGCAATGGAACTCGGGCAGAGCGCAGGGAAGCCTGTCACTTGCTTAAAAGATTACGTCCAGCGGTTTTCCAAT... |
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