Annotation Detail
Information
- Associated Genes
- RBM20
- Associated Variants
-
RBM20 p.Ser637Gly (p.S637G)
(
ENST00000369519.4 )
RBM20 p.Ser637Gly (p.S637G) ( ENST00000369519.4 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_001134363.3(RBM20):c.1909A>G (p.Ser637Gly) AND not provided
- ClinVar Allele ID
- 15311
- ClinVar RefSeq Alternation Syntax
- NM_001134363.3:c.1909A>G
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2019-11-20
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001753393
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs