Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K
Location

Chromosome 22:50570928 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Synonyms

Uniprot VAR_011740

HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 11 transcripts and has 1 sample genotype.

Variant displays