Original source

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

Alleles
A/G/T|Ancestral: A|Ambiguity code: D|MAF: 0.02 (G)
Location

Chromosome 22:23290360 (forward strand)|View in location tab

Co-located variant

COSMIC COSM5020861

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_041886

HGVS names

This variant has 16 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

Variant displays