Original source

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

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

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


with COSMIC COSM2156487 (G/A)

Most severe consequence
Missense variant
Evidence status

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

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 16 transcripts and 2 regulatory features.

Variant displays