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 16:3254762 (forward strand) | View in location tab


with COSMIC COSM435205 (A/G)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 23 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 15 transcripts, has 3771 sample genotypes, is associated with 1 phenotype and is mentioned in 4 citations.

Variant displays