Annotation Detail

Information
Associated Genes
ATM
Associated Variants
ATM p.Gly509GlufsTer3 (p.G509Efs*3) ( ENST00000601453.3, ENST00000713844.1, ENST00000531525.3, ENST00000278616.10, ENST00000452508.7, ENST00000675843.1 )
ATM p.Gly509GlufsTer3 (p.G509Efs*3) ( 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.1524del (p.Gly509fs) AND not provided
ClinVar Allele ID
186799
ClinVar RefSeq Alternation Syntax
NM_001351834.2:c.1524del
ClinVar RefSeq Alternation Syntax
NM_000051.4:c.1524del
Clinical Significance Description
Likely pathogenic
Clinical Significance Last Update
2016-02-29
Clinical Significance Review Status
criteria provided, single submitter
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000236634
ClinVar Disease
not provided
Observed Origin Sample
germline
Drugs