Original source

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

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.20 (G)

Chromosome 9:334337 (forward strand) | View in location tab


with COSMIC COSM3765452 (A/G), COSM3765451 (A/G)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 5 synonyms - Show

HGVS names

This variant has 16 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 9 transcripts, has 3995 sample genotypes and is associated with 1 phenotype.

Variant displays