Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.33 (A)

Chromosome 8:132897729 (forward strand) | View in location tab


with COSMIC COSM4162676 (A/G)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 4 synonyms - Show

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 4 transcripts, has 4074 sample genotypes, is associated with 2 phenotypes and is mentioned in 3 citations.

Variant displays