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

Co-located variants

COSMIC COSM5817, COSM5277, COSM5216, COSM5033 ; 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 5 phenotypes.

Variant displays