Original source

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

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

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

Co-located

with COSMIC COSM1682566 (G/A)

Most severe consequence
 
Missense variant
Synonyms

Uniprot VAR_064573

This variant has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts.

Variant displays