Original source

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

G/A | Ancestral: A | Ambiguity code: R | MAF: 0.31 (G)

Chromosome 16:3249749 (forward strand) | View in location tab


with COSMIC COSM3754868 (G/A), COSM3754869 (G/A)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


This variant has 4 synonyms - Show

HGVS names

This variant has 27 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 16 transcripts, has 2925 sample genotypes, is associated with 1 phenotype and is mentioned in 5 citations.

Variant displays