Annotation Detail
Information
- Associated Genes
- POU1F1
- Associated Variants
-
POU1F1 p.Glu276AsnfsTer2 (p.E276Nfs*2)
(
ENST00000344265.8,
ENST00000350375.7,
ENST00000560656.1 )
POU1F1 p.Glu276AsnfsTer2 (p.E276Nfs*2) ( ENST00000344265.8, ENST00000350375.7, ENST00000560656.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000306.4(POU1F1):c.747del (p.Glu250fs) AND not provided
- ClinVar Allele ID
- 28649
- ClinVar RefSeq Alternation Syntax
- NM_001122757.3:c.825del
- ClinVar RefSeq Alternation Syntax
- NM_000306.4:c.747del
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2022-12-26
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003556018
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs