Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/A/T | Ancestral: C | Ambiguity code: H
Location

Chromosome 5:136046406 (forward strand) | View in location tab

Co-located

with COSMIC COSM3769970 (C/T) ; HGMD-PUBLIC CM991173, CM971473

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 22912, 10443

This variant has 16 HGVS names - click the plus to show

About this variant

This variant overlaps 18 transcripts and is associated with 4 phenotypes.

Variant displays