Original source

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

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.38 (A)

Chromosome 7:10982603 (forward strand) | View in location tab


with COSMIC COSM3723031 (A/G), COSM3723030 (A/G)

Most severe consequence
Missense variant
Evidence status


This variant has 7 synonyms - Show

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 5 transcripts and has 3693 sample genotypes.

Variant displays