Original source

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

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

Chromosome X:38367331 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM950870

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 7413, OTC_AAA0000023

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 3 transcripts, is associated with 3 phenotypes and is mentioned in 2 citations.

Variant displays