Original source

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

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

Chromosome 5:35871088 (forward strand) | View in location tab


with COSMIC COSM149814 (G/A)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 10 synonyms - Show

HGVS names

This variant has 10 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 9 transcripts, has 4492 sample genotypes, is associated with 3 phenotypes and is mentioned in 22 citations.

Variant displays