Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome X:154563613 (forward strand) | View in location tab

Co-located

with PhenCode IKBKGbase_D0046:g.21349G>C (G/C)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

Uniprot VAR_042666

This variant has 19 HGVS names - click the plus to show

About this variant

This variant overlaps 14 transcripts, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays