Original source

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

A/G | Ancestral: A | Ambiguity code: R | MAF: 0.15 (G)

Chromosome 19:8975282 (forward strand) | View in location tab


with COSMIC COSM4132888 (A/G), COSM4132887 (A/G)

Most severe consequence
Missense variant
Evidence status


This variant has 2 synonyms - Show

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 1 transcript and has 4038 sample genotypes.

Variant displays