Annotation Detail
Information
- Associated Genes
- MRE11
- Associated Variants
-
MRE11 c.2070+2T>A
(
ENST00000393241.8,
ENST00000407439.7,
ENST00000323929.8,
ENST00000323977.7 )
MRE11 c.2070+2T>A ( ENST00000323929.8, ENST00000323977.7, ENST00000393241.8, ENST00000407439.7 ) - Associated Disease
- hereditary breast ovarian cancer syndrome
- Source Database
- ClinVar
- Description
- NM_005591.4(MRE11):c.2070+2T>A AND Hereditary breast ovarian cancer syndrome
- ClinVar Allele ID
- 183487
- ClinVar RefSeq Alternation Syntax
- NM_005591.4:c.2070+2T>A
- ClinVar RefSeq Alternation Syntax
- NM_001330347.2:c.2067+2T>A
- ClinVar RefSeq Alternation Syntax
- NM_005590.4:c.1986+2T>A
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2015-12-22
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000416696
- ClinVar Disease
- Hereditary breast ovarian cancer syndrome
- Observed Origin Sample
- unknown
Drugs