Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.44 (A)

Chromosome 13:46895805 (forward strand) | View in location tab


with COSMIC COSM3753711 (G/A) ; HGMD-PUBLIC CM960851

Most severe consequence
Synonymous variant
Evidence status


This variant has 5 HGVS names - click the plus to show

This variant has assays on 12 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts, has 4438 sample genotypes and is mentioned in 97 citations.

Variant displays