WormBase Tree Display for Variation: WBVar01618092
expand all nodes | collapse all nodes | view schema
WBVar01618092 | Name | Public_name | WBVar01618092 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00297669 | |||||||
F38G1.1.1:c.771+47T>C | ||||||||
HGVSg | CHROMOSOME_X:g.483412T>C | |||||||
Sequence_details | SMap | S_parent | Sequence | F38G1 | ||||
Flanking_sequences | AAAGAACTGAAACAATAATTTTTATTTCAA | TCATTTCAAATTTTTTCAAGGCCAACATCG | ||||||
Mapping_target | F38G1 | |||||||
Source_location | 225 | CHROMOSOME_X | 483413 | 483413 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | T | C | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain | WBStrain00006622 | From_analysis | Million_mutation_project_reanalysis | |||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00000484 | ||||||
Transcript | F38G1.1.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | F38G1.1.1:c.771+47T>C | |||||||
Intron_number | 6/15 | |||||||
Method | WGS_Flibotte |