Annotation Detail
Information
- Associated Genes
- MRE11
- Associated Variants
-
MRE11 p.Gln170Ter (p.Q170*)
(
ENST00000393241.8,
ENST00000407439.7,
ENST00000323929.8,
ENST00000323977.7,
ENST00000540013.5 )
MRE11 p.Gln170Ter (p.Q170*) ( 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.508C>T (p.Gln170Ter) AND Hereditary cancer-predisposing syndrome
- ClinVar Allele ID
- 151527
- ClinVar RefSeq Alternation Syntax
- NM_001330347.2:c.508C>T
- ClinVar RefSeq Alternation Syntax
- NM_005591.4:c.508C>T
- ClinVar RefSeq Alternation Syntax
- NM_005590.4:c.508C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2020-08-03
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000130478
- ClinVar Disease
- Hereditary cancer-predisposing syndrome
- Observed Origin Sample
- germline
Drugs