Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R
Location

Chromosome X:43728231 (forward strand)|View in location tab

Co-located variant

COSMIC COSM1682566

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_064573

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 3 transcripts.

Variant displays