Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ambiguity code: Y
Location

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

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_031554

This variant has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 35 sample genotypes.

Variant displays