Original source

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

G/C | Ancestral: G | Ambiguity code: S | MAF: 0.18 (C)

Chromosome 17:61456507 (forward strand) | View in location tab


with COSMIC COSM3755734 (G/C)

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_020251

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature, has 2775 sample genotypes and is mentioned in 5 citations.

Variant displays