Annotation Detail
Information
- Associated Genes
- VHL LOC107303340
- Associated Variants
-
VHL p.Arg167Gly (p.R167G)
(
ENST00000256474.3,
ENST00000345392.3,
ENST00000696143.2,
ENST00000696153.1,
ENST00000713811.1,
ENST00000713812.1,
ENST00000713815.1,
ENST00000713982.1 )
VHL p.Arg167Gly (p.R167G) ( ENST00000256474.3, ENST00000345392.3, ENST00000696143.2, ENST00000696153.1, ENST00000713811.1, ENST00000713812.1, ENST00000713815.1, ENST00000713982.1 ) - Associated Disease
- Hereditary cancer-predisposing syndrome
- Source Database
- ClinVar
- Description
- NM_000551.4(VHL):c.499C>G (p.Arg167Gly) AND Hereditary cancer-predisposing syndrome
- ClinVar Allele ID
- 17258
- ClinVar RefSeq Alternation Syntax
- NM_001354723.2:c.*53C>G
- ClinVar RefSeq Alternation Syntax
- NM_000551.4:c.499C>G
- ClinVar RefSeq Alternation Syntax
- NM_198156.3:c.376C>G
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2021-10-26
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002336073
- ClinVar Disease
- Hereditary cancer-predisposing syndrome
- Observed Origin Sample
- germline
Drugs