Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/G/T|Ancestral: C|Ambiguity code: B
Location

Chromosome X:153694424 (forward strand)|View in location tab

Co-located variants

COSMIC COSM3235790 ; HGMD-PUBLIC CM065469

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 6721

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 20 transcripts and is associated with 2 phenotypes.

Variant displays