Annotation Detail
Information
- Associated Genes
- RB1
- Associated Variants
-
RB1 p.Arg556Ter (p.R556*)
(
ENST00000713856.1,
ENST00000267163.6,
ENST00000650461.1,
ENST00000713857.1,
ENST00000713858.1 )
RB1 p.Arg556Ter (p.R556*) ( ENST00000267163.6, ENST00000650461.1, ENST00000713856.1, ENST00000713857.1, ENST00000713858.1 ) - Associated Disease
- Hereditary cancer-predisposing syndrome
- Source Database
- ClinVar
- Description
- NM_000321.3(RB1):c.1666C>T (p.Arg556Ter) AND Hereditary cancer-predisposing syndrome
- ClinVar Allele ID
- 28129
- ClinVar RefSeq Alternation Syntax
- NM_000321.3:c.1666C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2021-11-24
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000492084
- ClinVar Disease
- Hereditary cancer-predisposing syndrome
- Observed Origin Sample
- germline
Drugs