WormBase Tree Display for Variation: WBVar00056655
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WBVar00056655 | Name | Public_name | WBVar00056655 | ||
---|---|---|---|---|---|
Other_name | pas22928 | ||||
cewivar00106706 | |||||
B0336.7b.1:c.765-206G>A | |||||
B0336.7a.1:c.1035-206G>A | |||||
HGVSg | CHROMOSOME_III:g.5695460C>T | ||||
Sequence_details | SMap | S_parent | Sequence | B0336 | |
Flanking_sequences | CCCCGACTGAAACTTTATGGCAACCGTACCCTCCGGTTACGGTAGATTTT | TTTTCTCTTGACAATCGGAGGTTTAAAAAATAAAAATTAAAATTGTGGAA | |||
Mapping_target | B0336 | ||||
Type_of_mutation | Substitution | C | T | ||
SeqStatus | Sequenced | ||||
Variation_type | SNP | ||||
Predicted_SNP | |||||
Natural_variant | |||||
Origin | Species | Caenorhabditis elegans | |||
Strain (26) | |||||
Person | WBPerson6900 | ||||
Analysis | WGS_Pasadena_Quinlan | ||||
Million_mutation_project_reanalysis | |||||
WGS_Andersen | |||||
History | Acquires_merge | WBVar01445866 | |||
Status | Live | ||||
Affects | Gene | WBGene00015147 | |||
Transcript | B0336.7b.1 | VEP_consequence | intron_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | B0336.7b.1:c.765-206G>A | ||||
Intron_number | 5/6 | ||||
B0336.7a.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | B0336.7a.1:c.1035-206G>A | ||||
Intron_number | 6/7 | ||||
Method | WGS_Pasadena_Quinlan |