Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R
Location

Chromosome 12:52952312 (forward strand)|View in location tab

Co-located variant

COSMIC COSM2156487

Most severe consequence
 
Missense variant
Evidence status

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 16 transcripts and 2 regulatory features.

Variant displays