Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.30 (A)

Chromosome 12:13564574 (forward strand) | View in location tab


with COSMIC COSM430806 (G/A) ; HGMD-PUBLIC CM074898

Most severe consequence
Synonymous variant
Evidence status

Clinical significance

This variant has 4 synonyms - click the plus to show

This variant has 3 HGVS names - click the plus to show

This variant has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 4068 sample genotypes, is associated with 2 phenotypes and is mentioned in 17 citations.

Variant displays