Annotation Detail
Information
- Associated Genes
- VHL LOC107303340
- Associated Variants
-
VHL p.Asn150IlefsTer9 (p.N150Ifs*9)
(
ENST00000256474.3,
ENST00000345392.3,
ENST00000696143.2,
ENST00000696153.1,
ENST00000713811.1,
ENST00000713812.1,
ENST00000713815.1,
ENST00000713982.1 )
VHL p.Asn150IlefsTer9 (p.N150Ifs*9) ( 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.449del (p.Asn150fs) AND Von Hippel-Lindau syndrome
- ClinVar Allele ID
- 192254
- ClinVar RefSeq Alternation Syntax
- NM_198156.3:c.341-3165del
- ClinVar RefSeq Alternation Syntax
- NM_001354723.2:c.*18-3165del
- ClinVar RefSeq Alternation Syntax
- NM_000551.4:c.449del
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2018-08-01
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000767275
- ClinVar Disease
- Von Hippel-Lindau syndrome
- Observed Origin Sample
- germline
Drugs