Original source

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

G/A/C | Ancestral: G | Ambiguity code: V | MAF: 0.06 (A)

Chromosome 9:712766 (forward strand) | View in location tab


with COSMIC COSM1462722 (G/A), COSM1462721 (G/A)

Most severe consequence
Missense variant
Evidence status


This variant has 3 synonyms - Show

HGVS names

This variant has 22 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 12 transcripts and has 3434 sample genotypes.

Variant displays