Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.39 (G)

Chromosome 5:136052974 (forward strand) | View in location tab


with COSMIC COSM4159427 (A/G)

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 11 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 10 transcripts, 1 regulatory feature, has 2898 sample genotypes and is mentioned in 2 citations.

Variant displays