Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.46 (A)

Chromosome 6:39357302 (forward strand) | View in location tab


with COSMIC COSM150088 (A/G) ; HGMD-PUBLIC CM074911

Most severe consequence
Missense variant
Evidence status


This variant has 4 synonyms - Show

HGVS names

This variant has 11 HGVS names - Show

Genotyping chips

This variant has assays on 13 chips - Show

About this variant

This variant overlaps 6 transcripts, has 4444 sample genotypes and is mentioned in 38 citations.

Variant displays