Annotation Detail
Information
- Associated Genes
- POU1F1
- Associated Variants
-
POU1F1 p.Trp219Arg (p.W219R)
(
ENST00000344265.8,
ENST00000350375.7,
ENST00000560656.1 )
POU1F1 p.Trp219Arg (p.W219R) ( ENST00000344265.8, ENST00000350375.7, ENST00000560656.1 ) - Associated Disease
- Pituitary hormone deficiency, combined, 1
- Source Database
- ClinVar
- Description
- NM_000306.4(POU1F1):c.577T>C (p.Trp193Arg) AND Pituitary hormone deficiency, combined, 1
- ClinVar Allele ID
- 28650
- ClinVar RefSeq Alternation Syntax
- NM_000306.4:c.577T>C
- ClinVar RefSeq Alternation Syntax
- NM_001122757.3:c.655T>C
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2001-04-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000014581
- ClinVar Disease
- Pituitary hormone deficiency, combined, 1
- Observed Origin Sample
- germline
- Pubmed
- 11297581
Drugs