Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R
Location

Chromosome 3:87259959 (forward strand)|View in location tab

Co-located variants

COSMIC COSM263051 ; HGMD-PUBLIC CM920590

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 4688, 2010_April_001_139_POU1F1_173110_0002

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 6 transcripts, 2 regulatory features and is associated with 2 phenotypes.

Variant displays