Annotation Detail
Information
- Associated Genes
- RAD51B
- Associated Variants
-
RAD51B c.1037-43041C>T
(
ENST00000487270.5,
ENST00000488612.5,
ENST00000487861.5 )
RAD51B c.1037-43041C>T ( ENST00000487270.5, ENST00000487861.5, ENST00000488612.5 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_133509.5(RAD51B):c.1037-26520C>T AND not provided
- ClinVar Allele ID
- 227637
- ClinVar RefSeq Alternation Syntax
- NM_001321818.2:c.1036+99715C>T
- ClinVar RefSeq Alternation Syntax
- NM_001321821.2:c.1037-43041C>T
- ClinVar RefSeq Alternation Syntax
- NM_001321815.1:c.923-43193C>T
- ClinVar RefSeq Alternation Syntax
- NM_001321809.2:c.1037-34698C>T
- ClinVar RefSeq Alternation Syntax
- NM_133509.5:c.1037-26520C>T
- ClinVar RefSeq Alternation Syntax
- NM_001321810.2:c.1037-34698C>T
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2019-06-14
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001689744
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs