Annotation Detail
Information
- Associated Genes
- BRCA2
- Associated Variants
-
BRCA2 c.7977-1G>C
(
ENST00000713680.1,
ENST00000713678.1,
ENST00000700202.2,
ENST00000530893.7,
ENST00000380152.8,
ENST00000544455.6 )
BRCA2 c.7977-1G>C ( ENST00000380152.8, ENST00000530893.7, ENST00000544455.6, ENST00000700202.2, ENST00000713678.1, ENST00000713680.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000059.4(BRCA2):c.7977-1G>C AND not provided
- ClinVar Allele ID
- 46688
- ClinVar RefSeq Alternation Syntax
- NM_000059.4:c.7977-1G>C
- ClinVar RefSeq Alternation Syntax
- NM_001406719.1:c.7881-1G>C
- ClinVar RefSeq Alternation Syntax
- NM_001406720.1:c.7977-1G>C
- ClinVar RefSeq Alternation Syntax
- NM_001406721.1:c.3045-1G>C
- ClinVar RefSeq Alternation Syntax
- NM_001406722.1:c.1560-1G>C
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2023-08-15
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000486971
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs