Original source

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

C/T | Ancestral: C | Ambiguity code: Y

Chromosome 12:6845711 (forward strand) | View in location tab


with COSMIC COSM147403 (C/T) ; HGMD-PUBLIC CS983412

Most severe consequence
Synonymous variant
Evidence status


This variant has 9 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 21 transcripts, has 376 sample genotypes and is mentioned in 51 citations.

Variant displays