Annotation Detail
Information
- Associated Genes
- ATM
- Associated Variants
-
ATM p.Arg1882Ter (p.R1882*)
(
ENST00000713844.1,
ENST00000601453.3,
ENST00000675843.1,
ENST00000278616.10,
ENST00000452508.7 )
ATM p.Arg1882Ter (p.R1882*) ( ENST00000278616.10, ENST00000452508.7, ENST00000601453.3, ENST00000675843.1, ENST00000713844.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000051.4(ATM):c.5644C>T (p.Arg1882Ter) AND not provided
- ClinVar Allele ID
- 186802
- ClinVar RefSeq Alternation Syntax
- NM_001351834.2:c.5644C>T
- ClinVar RefSeq Alternation Syntax
- NM_000051.4:c.5644C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2023-01-06
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000235346
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs