Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.22 (G)

Chromosome 5:74689390 (forward strand) | View in location tab


with COSMIC COSM149850 (A/G), COSM3683901 (A/C)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 4 synonyms - Show

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 5 transcripts, has 3985 sample genotypes, is associated with 3 phenotypes and is mentioned in 1 citation.

Variant displays