Annotation Detail
Information
- Associated Genes
- MRE11
- Associated Variants
-
MRE11 p.Asp8Ter (p.D8*)
(
ENST00000323977.7,
ENST00000323929.8,
ENST00000393241.8,
ENST00000407439.7,
ENST00000540013.5 )
MRE11 p.Asp8Ter (p.D8*) ( ENST00000323929.8, ENST00000323977.7, ENST00000393241.8, ENST00000407439.7, ENST00000540013.5 ) - Associated Disease
- Hereditary cancer-predisposing syndrome
- Source Database
- ClinVar
- Description
- NM_005591.4(MRE11):c.21-6_26del AND Hereditary cancer-predisposing syndrome
- ClinVar Allele ID
- 133436
- ClinVar RefSeq Alternation Syntax
- NM_005591.4:c.21-6_26del
- ClinVar RefSeq Alternation Syntax
- NM_005590.4:c.21-6_26del
- ClinVar RefSeq Alternation Syntax
- NM_001330347.2:c.21-6_26del
- Clinical Significance Description
- Conflicting interpretations of pathogenicity
- Clinical Significance Last Update
- 2022-10-17
- Clinical Significance Review Status
- criteria provided, conflicting interpretations
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000115914
- ClinVar Disease
- Hereditary cancer-predisposing syndrome
- Observed Origin Sample
- germline
Drugs