Original source

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

T/G | Ancestral: G | Ambiguity code: K | MAF: 0.49 (G)

Chromosome 12:52469837 (forward strand) | View in location tab


with COSMIC COSM3753348 (T/G)

Most severe consequence
Synonymous variant
Evidence status


Archive dbSNP rs11540296, rs61190875

This variant has 2 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 3 transcripts and has 2513 sample genotypes.

Variant displays