Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.04 (A)

Chromosome 6:111591867 (forward strand) | View in location tab


with COSMIC COSM3736397 (G/A)

Most severe consequence
Missense variant
Evidence status


This variant has 2 synonyms - Show

HGVS names

This variant has 12 HGVS names - Show

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 9 transcripts, 1 regulatory feature, has 3871 sample genotypes and is mentioned in 9 citations.

Variant displays