Annotation Detail
Information
- Associated Genes
- ATM
- Associated Variants
-
ATM c.1066-6T>G
(
ENST00000675843.1,
ENST00000278616.10,
ENST00000601453.3,
ENST00000452508.7,
ENST00000531525.3,
ENST00000713844.1 )
ATM c.1066-6T>G ( ENST00000278616.10, ENST00000452508.7, ENST00000531525.3, ENST00000601453.3, ENST00000675843.1, ENST00000713844.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000051.4(ATM):c.1066-6T>G AND not provided
- ClinVar Allele ID
- 18077
- ClinVar RefSeq Alternation Syntax
- NM_000051.4:c.1066-6T>G
- ClinVar RefSeq Alternation Syntax
- NM_001351834.2:c.1066-6T>G
- Clinical Significance Description
- Conflicting interpretations of pathogenicity
- Clinical Significance Last Update
- 2024-02-01
- Clinical Significance Review Status
- criteria provided, conflicting interpretations
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000488246
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
- Observed Origin Sample
- unknown
Drugs