Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: < 0.01 (C)

Chromosome 12:21635657 (forward strand) | View in location tab


with COSMIC COSM3931606 (T/C)

Most severe consequence
Missense variant
Evidence status

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 2504 sample genotypes.

Variant displays