Annotation Detail
Information
- Associated Genes
- BRCA2
- Associated Variants
-
BRCA2 p.Arg3128Ter (p.R3128*)
(
ENST00000380152.8,
ENST00000544455.6,
ENST00000530893.7,
ENST00000700202.2,
ENST00000713678.1,
ENST00000713680.1 )
BRCA2 p.Arg3128Ter (p.R3128*) ( ENST00000380152.8, ENST00000530893.7, ENST00000544455.6, ENST00000700202.2, ENST00000713678.1, ENST00000713680.1 ) - Associated Disease
- Wilms tumor 1 Familial cancer of breast Pancreatic cancer, susceptibility to, 2 Fanconi anemia complementation group D1 Breast-ovarian cancer, familial, susceptibility to, 2 Glioma susceptibility 3 medulloblastoma Malignant tumor of prostate
- Source Database
- ClinVar
- Description
- NM_000059.4(BRCA2):c.9382C>T (p.Arg3128Ter) AND multiple conditions
- ClinVar Allele ID
- 67494
- ClinVar RefSeq Alternation Syntax
- NM_000059.4:c.9382C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2018-10-31
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000763332
- ClinVar Disease
- Fanconi anemia complementation group D1
- ClinVar Disease
- Malignant tumor of prostate
- ClinVar Disease
- Medulloblastoma
- ClinVar Disease
- Wilms tumor 1
- ClinVar Disease
- Breast-ovarian cancer, familial, susceptibility to, 2
- ClinVar Disease
- Familial cancer of breast
- ClinVar Disease
- Pancreatic cancer, susceptibility to, 2
- ClinVar Disease
- Glioma susceptibility 3
- Observed Origin Sample
- unknown
Drugs