Annotation Detail
Information
- Associated Genes
- PKHD1 LOC126859690
- Associated Variants
-
PKHD1 p.Val1741Met (p.V1741M)
(
ENST00000340994.4,
ENST00000371117.8 )
PKHD1 p.Val1741Met (p.V1741M) ( ENST00000340994.4, ENST00000371117.8 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_138694.4(PKHD1):c.5221G>A (p.Val1741Met) AND not provided
- ClinVar Allele ID
- 19150
- ClinVar RefSeq Alternation Syntax
- NM_138694.4:c.5221G>A
- ClinVar RefSeq Alternation Syntax
- NM_170724.3:c.5221G>A
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2023-08-28
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000153715
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs