Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

G/A/C | Ancestral: G | Ambiguity code: V

Chromosome 10:87933148 (forward strand) | View in location tab


with COSMIC COSM5817 (G/-), COSM5033 (G/A), COSM5277 (G/C), COSM5216 (G/T) ; HGMD-PUBLIC CM991081, CM981670 ; dbSNP rs121913292 (G/-)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 18 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and is associated with 4 phenotypes.

Variant displays