Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.46 (C)

Chromosome 7:2538147 (forward strand) | View in location tab


with COSMIC COSM452894 (T/C)

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

Variant displays