Original source

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

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

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

Co-located variant

COSMIC COSM3931606

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