Original source

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

G/A | Ancestral: G | Ambiguity code: R

Chromosome 12:6845700 (forward strand) | View in location tab


with COSMIC COSM3736074 (G/A) ; HGMD-PUBLIC CM117875

Most severe consequence
Missense variant
Evidence status


This variant has 7 synonyms - Show

HGVS names

This variant has 12 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 21 transcripts, has 3285 sample genotypes and is mentioned in 2 citations.

Variant displays