Annotation Detail
Information
- Associated Genes
- ATM
- Associated Variants
-
ATM p.Gln1839Ter (p.Q1839*)
(
ENST00000713844.1,
ENST00000601453.3,
ENST00000452508.7,
ENST00000278616.10,
ENST00000675843.1 )
ATM p.Gln1839Ter (p.Q1839*) ( ENST00000278616.10, ENST00000452508.7, ENST00000601453.3, ENST00000675843.1, ENST00000713844.1 ) - Associated Disease
- Hereditary cancer-predisposing syndrome
- Source Database
- ClinVar
- Description
- NM_000051.4(ATM):c.5515C>T (p.Gln1839Ter) AND Hereditary cancer-predisposing syndrome
- ClinVar Allele ID
- 186801
- ClinVar RefSeq Alternation Syntax
- NM_000051.4:c.5515C>T
- ClinVar RefSeq Alternation Syntax
- NM_001351834.2:c.5515C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2023-05-23
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000777919
- ClinVar Disease
- Hereditary cancer-predisposing syndrome
- Observed Origin Sample
- germline
Drugs