Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome X:153784559 (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

Synonyms

Uniprot VAR_026494

This variation has 33 HGVS names - click the plus to show

Variation displays