Original source

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

Alleles
G/A|Ambiguity code: R
Location

Chromosome 12:52287624 (forward strand)|View in location tab

Co-located variant

COSMIC COSM4042813

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Archive dbSNP rs75304109

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays