Annotation Detail
Information
- Associated Genes
- MRE11
- Associated Variants
-
MRE11 c.1867+2T>C
(
ENST00000323977.7,
ENST00000323929.8,
ENST00000393241.8,
ENST00000407439.7 )
MRE11 c.1867+2T>C ( ENST00000323929.8, ENST00000323977.7, ENST00000393241.8, ENST00000407439.7 ) - Associated Disease
- Hereditary cancer-predisposing syndrome
- Source Database
- ClinVar
- Description
- NM_005591.4(MRE11):c.1867+2T>C AND Hereditary cancer-predisposing syndrome
- ClinVar Allele ID
- 183495
- ClinVar RefSeq Alternation Syntax
- NM_005590.4:c.1783+1411T>C
- ClinVar RefSeq Alternation Syntax
- NM_005591.4:c.1867+2T>C
- ClinVar RefSeq Alternation Syntax
- NM_001330347.2:c.1864+2T>C
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2022-11-30
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000166874
- ClinVar Disease
- Hereditary cancer-predisposing syndrome
- Observed Origin Sample
- germline
Drugs