Annotation Detail
Information
- Associated Genes
- PKHD1
- Associated Variants
-
PKHD1 p.Trp2398Ter (p.W2398*)
(
ENST00000340994.4,
ENST00000371117.8 )
PKHD1 p.Trp2398Ter (p.W2398*) ( ENST00000340994.4, ENST00000371117.8 ) - Associated Disease
- autosomal recessive polycystic kidney disease
- Source Database
- ClinVar
- Description
- NM_138694.4(PKHD1):c.7194G>A (p.Trp2398Ter) AND Autosomal recessive polycystic kidney disease
- ClinVar Allele ID
- 194695
- ClinVar RefSeq Alternation Syntax
- NM_170724.3:c.7194G>A
- ClinVar RefSeq Alternation Syntax
- NM_138694.4:c.7194G>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2023-02-24
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003611503
- ClinVar Disease
- Autosomal recessive polycystic kidney disease
- Observed Origin Sample
- germline
Drugs