Original source

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

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

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

Co-located

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

Most severe consequence
Evidence status

Synonyms

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

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

About this variant

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

Variation displays