Annotation Detail
Information
- Associated Genes
- VHL LOC107303340
- Associated Variants
-
VHL p.Pro192Ser (p.P192S)
(
ENST00000256474.3,
ENST00000345392.3,
ENST00000696143.2,
ENST00000696153.1,
ENST00000713811.1,
ENST00000713812.1,
ENST00000713815.1,
ENST00000713982.1 )
VHL p.Pro192Ser (p.P192S) ( ENST00000256474.3, ENST00000345392.3, ENST00000696143.2, ENST00000696153.1, ENST00000713811.1, ENST00000713812.1, ENST00000713815.1, ENST00000713982.1 ) - Associated Disease
- Von Hippel-Lindau syndrome
- Source Database
- ClinVar
- Description
- NM_000551.4(VHL):c.574C>T (p.Pro192Ser) AND Von Hippel-Lindau syndrome
- ClinVar Allele ID
- 17273
- ClinVar RefSeq Alternation Syntax
- NM_198156.3:c.451C>T
- ClinVar RefSeq Alternation Syntax
- NM_000551.4:c.574C>T
- ClinVar RefSeq Alternation Syntax
- NM_001354723.2:c.*128C>T
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2023-12-01
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003996075
- ClinVar Disease
- Von Hippel-Lindau syndrome
- Observed Origin Sample
- germline
Drugs