Original source

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

T/C | Ambiguity code: Y | MAF: 0.38 (C)

Chromosome 12:52316099 (forward strand) | View in location tab


with COSMIC COSM147521 (T/C)

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

Variant displays