Original source

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

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

Chromosome 12:13563041 (forward strand) | View in location tab


with COSMIC COSM3998717 (A/G)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


LSDB NC_000012.11:g.13715975A>G

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 2 transcripts, has 3807 sample genotypes, is associated with 1 phenotype and is mentioned in 9 citations.

Variant displays