WormBase Tree Display for Variation: WBVar00038281
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WBVar00038281 | Name | Public_name | WBVar00038281 | ||
---|---|---|---|---|---|
Other_name | pas19253 | ||||
cewivar00606586 | |||||
F56D12.1b.1:c.*329G>T | |||||
F56D12.1a.1:c.1476-176G>T | |||||
F56D12.1d.1:c.1056-176G>T | |||||
F56D12.1a.2:c.1476-176G>T | |||||
HGVSg | CHROMOSOME_II:g.1306777C>A | ||||
Sequence_details | SMap | S_parent | Sequence | F56D12 | |
Flanking_sequences | caccggccttatcattggttccggacaatctggagcctccgaatggctgctggccgacgattgatccagttgatttgtcgttgaggtacatgttgccgacggcgtcgcggagaacatcgcgagctctgagaaaaaaaaacactttgttgaaaaacgtttttaacacaaaaattcgcctcaaaaatctcgaaaaatcgatcgaaatccaacaaaaattccaataaaaaataccgtagccctttaaagggacacacactttcactgttgggtctcgccacgctcaggaacatcttactgtcg | tttcaaattttttgtttgttgttatcgcttttttttttcgatttttgccagtttttctagcttttcatttgatttgtgacgaaattcgagggtttttattggagaaattgtgtaattatcgtttttcgacattttttaacctattttgttcggttatagagaaatttcttgaaaattgccgaaaaaacagaatttcaagatttcgaattttccgggaataattttaaatcgacttttggcagttttcttgtgcctaaaatgttgaatttcagcatttttgaacataacaaacccgaaaat | |||
Mapping_target | F56D12 | ||||
Type_of_mutation | Substitution | C | A | ||
SeqStatus | Sequenced | ||||
Variation_type | SNP | ||||
Predicted_SNP | |||||
Natural_variant | |||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00004604 | From_analysis | WGS_Pasadena_Quinlan | ||
WBStrain00023665 | From_analysis | Million_mutation_project_reanalysis | |||
Person | WBPerson6900 | ||||
Analysis | WGS_Pasadena_Quinlan | ||||
Million_mutation_project_reanalysis | |||||
Status | Live | ||||
Affects | Gene | WBGene00000112 | |||
Transcript | F56D12.1b.1 | VEP_consequence | 3_prime_UTR_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | F56D12.1b.1:c.*329G>T | ||||
cDNA_position | 1870 | ||||
Exon_number | 8/8 | ||||
F56D12.1a.2 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | F56D12.1a.2:c.1476-176G>T | ||||
Intron_number | 8/9 | ||||
F56D12.1a.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | F56D12.1a.1:c.1476-176G>T | ||||
Intron_number | 7/8 | ||||
F56D12.1d.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | F56D12.1d.1:c.1056-176G>T | ||||
Intron_number | 3/3 | ||||
Method | WGS_Pasadena_Quinlan |