Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.40 (C)

Chromosome 12:6537154 (forward strand) | View in location tab


with COSMIC COSM3998914 (T/C)

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 17 HGVS names - Show

About this variant

This variant overlaps 25 transcripts and has 2526 sample genotypes.

Variant displays