Annotation Detail
Information
- Associated Genes
- RAD51 LOC130056864
- Associated Variants
-
RAD51 c.-98G>C
(
ENST00000382643.7,
ENST00000423169.6,
ENST00000557850.5,
ENST00000645673.2,
ENST00000267868.8 )
RAD51 c.-98G>C ( ENST00000267868.8, ENST00000382643.7, ENST00000423169.6, ENST00000557850.5, ENST00000645673.2 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_002875.5(RAD51):c.-98G>C AND not provided
- ClinVar Allele ID
- 28167
- ClinVar RefSeq Alternation Syntax
- NM_002875.5:c.-98G>C
- ClinVar RefSeq Alternation Syntax
- NM_133487.4:c.-98G>C
- ClinVar RefSeq Alternation Syntax
- NM_001164269.2:c.-3+9G>C
- ClinVar RefSeq Alternation Syntax
- NM_001164270.2:c.-98G>C
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-06-22
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001642223
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs