WormBase Tree Display for Variation: WBVar00432364
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WBVar00432364 | Name | Public_name | gk209121 | ||
---|---|---|---|---|---|
Other_name (12) | |||||
HGVSg | CHROMOSOME_IV:g.9544878G>A | ||||
Sequence_details | SMap | S_parent | Sequence | T05A1 | |
Flanking_sequences | TGATTACCTTTACGCTAACCCTAGCCCACCTAATTTCAGGTGCTCCAAAC | TTCTTCCAGCTATTCGAGCTAATTTTTTACTTCAAAAAGGTGAAAAACGA | |||
Mapping_target | T05A1 | ||||
Type_of_mutation | Substitution | G | A | ||
SeqStatus | Sequenced | ||||
Variation_type | Allele | ||||
Origin | Species | Caenorhabditis elegans | |||
Strain | WBStrain00038404 | ||||
Laboratory | VC | ||||
Analysis | Million_Mutation_Project | ||||
Status | Live | ||||
Affects | Gene | WBGene00001403 | |||
Transcript | F56H11.1e.1 | VEP_consequence | intron_variant | ||
VEP_impact | MODIFIER | ||||
HGVSc | F56H11.1e.1:c.1554-456G>A | ||||
Intron_number | 10/11 | ||||
F56H11.1d.1 (12) | |||||
F56H11.1a.1 (12) | |||||
F56H11.1g.1 (12) | |||||
F56H11.1h.1 (12) | |||||
F56H11.1c.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | F56H11.1c.1:c.1806-456G>A | ||||
Intron_number | 13/15 | ||||
F56H11.1f.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | F56H11.1f.1:c.1437-456G>A | ||||
Intron_number | 10/11 | ||||
F56H11.1b.1 | VEP_consequence | intron_variant | |||
VEP_impact | MODIFIER | ||||
HGVSc | F56H11.1b.1:c.1689-456G>A | ||||
Intron_number | 13/15 | ||||
Reference | WBPaper00042537 | ||||
Method | Million_mutation |