Annotation Detail
Information
- Associated Genes
- RAD51B
- Associated Variants
-
RAD51B c.757-98173T>C
(
ENST00000471583.6,
ENST00000487861.5,
ENST00000488612.5,
ENST00000460526.6,
ENST00000487270.5 )
RAD51B c.757-98173T>C ( ENST00000460526.6, ENST00000471583.6, ENST00000487270.5, ENST00000487861.5, ENST00000488612.5 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_133510.4(RAD51B):c.757-98173T>C AND not provided
- ClinVar Allele ID
- 227636
- ClinVar RefSeq Alternation Syntax
- NM_001321818.2:c.757-98173T>C
- ClinVar RefSeq Alternation Syntax
- NM_001321819.1:c.757-98173T>C
- ClinVar RefSeq Alternation Syntax
- NM_001321815.1:c.643-98173T>C
- ClinVar RefSeq Alternation Syntax
- NM_133510.4:c.757-98173T>C
- ClinVar RefSeq Alternation Syntax
- NM_001321809.2:c.757-98173T>C
- ClinVar RefSeq Alternation Syntax
- NM_001321817.2:c.400-98173T>C
- ClinVar RefSeq Alternation Syntax
- NM_001321821.2:c.757-98173T>C
- ClinVar RefSeq Alternation Syntax
- NM_133509.5:c.757-98173T>C
- ClinVar RefSeq Alternation Syntax
- NM_001321814.2:c.757-98173T>C
- ClinVar RefSeq Alternation Syntax
- NM_002877.6:c.757-98173T>C
- ClinVar RefSeq Alternation Syntax
- NM_001321810.2:c.757-98173T>C
- ClinVar RefSeq Alternation Syntax
- NM_001321812.1:c.757-98173T>C
- 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/RCV001594875
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs