Original source

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

A/C | Ancestral: A | Ambiguity code: M

Chromosome 12:90964283 (forward strand) | View in location tab


with COSMIC COSM4045347 (A/G)

Most severe consequence
Missense variant
HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 262 sample genotypes.

Variant displays