Annotation Detail
Information
- Associated Genes
- PKHD1 LOC126859690
- Associated Variants
-
PKHD1 p.Arg1624Trp (p.R1624W)
(
ENST00000340994.4,
ENST00000371117.8 )
PKHD1 p.Arg1624Trp (p.R1624W) ( ENST00000340994.4, ENST00000371117.8 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_138694.4(PKHD1):c.4870C>T (p.Arg1624Trp) AND not provided
- ClinVar Allele ID
- 186055
- ClinVar RefSeq Alternation Syntax
- NM_138694.4:c.4870C>T
- ClinVar RefSeq Alternation Syntax
- NM_170724.3:c.4870C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2023-09-29
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000479548
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs