Original source

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

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

Chromosome X:83509291 (forward strand) | View in location tab

Co-located

with COSMIC COSM4111298 (C/T), COSM4111297 (C/T) ; HGMD-PUBLIC CM005401

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 6741, 2010_April_001_314_POU3F4_300039_0009

This variant has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts and is associated with 3 phenotypes.

Variant displays