Original source

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

Alleles
G/A | Ambiguity code: R
Location

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

Co-located

with COSMIC COSM4042813 (G/A)

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Archive dbSNP rs75304109

This variant has 7 HGVS names - click the plus to 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