Original source

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

C/T | Ambiguity code: Y

Chromosome 22:23312944 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_031554

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 35 sample genotypes.

Variant displays