Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | 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
Evidence status

Synonyms

Uniprot VAR_064573

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

Variation displays