Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome X:154556344 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM042369 ; PhenCode IKBKGbase_D0046:g.14079C>T (C/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

Uniprot VAR_026494

This variation has 31 HGVS names - click the plus to show

Variation displays