Annotation Detail
Information
- Associated Genes
- BARD1
- Associated Variants
-
BARD1 p.Pro657HisfsTer57 (p.P657Hfs*57)
(
ENST00000260947.9,
ENST00000421162.2,
ENST00000613374.5,
ENST00000613706.5,
ENST00000617164.5,
ENST00000619009.5,
ENST00000620057.4 )
BARD1 p.Pro657HisfsTer57 (p.P657Hfs*57) ( ENST00000260947.9, ENST00000421162.2, ENST00000613374.5, ENST00000613706.5, ENST00000617164.5, ENST00000619009.5, ENST00000620057.4 ) - Associated Disease
- Familial cancer of breast
- Source Database
- ClinVar
- Description
- NM_000465.4(BARD1):c.1970del (p.Pro657fs) AND Familial cancer of breast
- ClinVar Allele ID
- 181768
- ClinVar RefSeq Alternation Syntax
- NM_000465.4:c.1970del
- ClinVar RefSeq Alternation Syntax
- NM_001282543.2:c.1913del
- ClinVar RefSeq Alternation Syntax
- NR_104216.2:n.1134del
- ClinVar RefSeq Alternation Syntax
- NM_001282545.2:c.617del
- ClinVar RefSeq Alternation Syntax
- NM_001282548.2:c.560del
- ClinVar RefSeq Alternation Syntax
- NR_104215.2:n.1878del
- ClinVar RefSeq Alternation Syntax
- NM_001282549.2:c.431del
- ClinVar RefSeq Alternation Syntax
- NR_104212.2:n.1935del
- Clinical Significance Description
- Pathogenic/Likely pathogenic
- Clinical Significance Last Update
- 2023-05-25
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001377223
- ClinVar Disease
- Familial cancer of breast
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs