Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

G/A | Ambiguity code: R

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


with COSMIC COSM4042813 (G/A) ; dbSNP rs75304109 (A/G)

Most severe consequence
Evidence status

This variation has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 1 individual genotype.

Variation displays