Original source

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

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

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

Most severe consequence
Missense variant
Evidence status


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