Original source

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

Alleles
A/C/G|Ancestral: A|Ambiguity code: V
Location

Chromosome 22:23261461 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_051983

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 16 transcripts, has 261 sample genotypes and is mentioned in 1 citation.

Variant displays