Original source

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

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

Chromosome 5:112840628 (forward strand) | View in location tab


with COSMIC COSM3760870 (G/A)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 14 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 11 transcripts, has 3799 sample genotypes, is associated with 3 phenotypes and is mentioned in 10 citations.

Variant displays