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Gene | ATM |
Variant | A59S |
Impact List | missense |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | ATM A59S does not lie within any known functional domains of the Atm protein (UniProt.org). A59S results in impaired ability to rescue survival of ATM-deficient cells upon irradiation in culture (PMID: 29059438), and therefore, is predicted to lead to a loss of Atm protein function. |
Associated Drug Resistance | |
Category Variants Paths |
ATM mutant ATM inact mut ATM A59S |
Transcript | NM_000051.4 |
gDNA | chr11:g.108227878G>T |
cDNA | c.175G>T |
Protein | p.A59S |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_017017792 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_005271562 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
NM_000051.3 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
NM_000051.4 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_011542842 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_047426976.1 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_011542842.3 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
NM_001351834.1 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
NM_001351835.2 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_017017789 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_017017790.3 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_017017789.2 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
NM_000051 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_047426977.1 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_017017791.1 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
NM_001351836.1 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_011542843.3 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_005271562.6 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_047426975.1 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_011542843.2 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
NM_001351836.2 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_005271562.5 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_005271561 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_011542840.3 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_047426978.1 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_006718843 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_011542840 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_047426979.1 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_017017790.2 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_047426981.1 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_017017790 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_011542842.4 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_011542840.4 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_006718843.5 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_017017792.2 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_017017791 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
NM_001351834.2 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_006718843.4 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
NM_001351835.1 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
XM_011542843 | chr11:g.108227878G>T | c.175G>T | p.A59S | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
---|---|---|---|---|---|---|---|
ATM A59S | neuroblastoma | sensitive | Olaparib | Preclinical - Cell culture | Actionable | In a preclinical study, Lynparza (olaparib) treatment of neuroblastoma cells in culture, transfected with Atm A59S, resulted in decreased cell viability as compared to cells carrying wild-type Atm (PMID: 29059438). | 29059438 |