Annotation Detail
Information
- Associated Genes
- PKHD1
- Associated Variants
-
PKHD1 p.Thr36Met (p.T36M)
(
ENST00000340994.4,
ENST00000371117.8 )
PKHD1 p.Thr36Met (p.T36M) ( ENST00000340994.4, ENST00000371117.8 ) - Associated Disease
- Inborn genetic diseases
- Source Database
- ClinVar
- Description
- NM_138694.4(PKHD1):c.107C>T (p.Thr36Met) AND Inborn genetic diseases
- ClinVar Allele ID
- 19147
- ClinVar RefSeq Alternation Syntax
- NM_138694.4:c.107C>T
- ClinVar RefSeq Alternation Syntax
- NM_170724.3:c.107C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2022-06-02
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV004018552
- ClinVar Disease
- Inborn genetic diseases
- Observed Origin Sample
- germline
Drugs