Annotation Detail

Information
Associated Genes
ATM C11orf65
Associated Variants
ATM p.Glu2052Lys (p.E2052K) ( ENST00000452508.7, ENST00000278616.10, ENST00000675843.1, ENST00000713844.1, ENST00000525729.5, ENST00000601453.3 )
ATM p.Glu2052Lys (p.E2052K) ( ENST00000278616.10, ENST00000452508.7, ENST00000601453.3, ENST00000675843.1, ENST00000713844.1, ENST00000525729.5 )
Associated Disease
not provided
Source Database
ClinVar
Description
NM_000051.4(ATM):c.6154G>A (p.Glu2052Lys) AND not provided
ClinVar Allele ID
180484
ClinVar RefSeq Alternation Syntax
NM_001351110.2:c.*39-6998C>T
ClinVar RefSeq Alternation Syntax
NM_001330368.2:c.641-6998C>T
ClinVar RefSeq Alternation Syntax
NM_000051.4:c.6154G>A
ClinVar RefSeq Alternation Syntax
NM_001351834.2:c.6154G>A
Clinical Significance Description
Conflicting interpretations of pathogenicity
Clinical Significance Last Update
2022-09-16
Clinical Significance Review Status
criteria provided, conflicting interpretations
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000212039
ClinVar Disease
not provided
Observed Origin Sample
germline
Observed Origin Sample
unknown
Drugs