WormBase Tree Display for Variation: WBVar01804625
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WBVar01804625 | Name | Public_name | WBVar01804625 | |||||
---|---|---|---|---|---|---|---|---|
Other_name | cewivar00515497 | |||||||
F09E8.7a.1:c.1035+194A>G | ||||||||
F09E8.7b.1:c.960+194A>G | ||||||||
HGVSg | CHROMOSOME_IV:g.13175948T>C | |||||||
Sequence_details | SMap | S_parent | Sequence | F58D2 | ||||
Flanking_sequences | TTAATGAAAATTGATTTTTTCGTGTATTTT | CGAAACATTTCTTTTTATTTTTTGGAAAAA | ||||||
Mapping_target | F58D2 | |||||||
Source_location | 225 | CHROMOSOME_IV | 13175924 | 13175924 | From_analysis | Million_mutation_project_reanalysis | ||
Type_of_mutation | Substitution | T | C | |||||
SeqStatus | Sequenced | |||||||
Variation_type | Natural_variant | |||||||
Origin | Species | Caenorhabditis elegans | ||||||
Strain (2) | ||||||||
Laboratory | VC | |||||||
Analysis | Million_mutation_project_reanalysis | |||||||
Status | Live | |||||||
Affects | Gene | WBGene00002974 | ||||||
Transcript | F09E8.7a.1 | VEP_consequence | intron_variant | |||||
VEP_impact | MODIFIER | |||||||
HGVSc | F09E8.7a.1:c.1035+194A>G | |||||||
Intron_number | 5/9 | |||||||
F09E8.7b.1 | VEP_consequence | intron_variant | ||||||
VEP_impact | MODIFIER | |||||||
HGVSc | F09E8.7b.1:c.960+194A>G | |||||||
Intron_number | 6/10 | |||||||
Method | WGS_Flibotte |