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Gene | ATM |
Variant | S2017T |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | ATM S2017T lies within the FAT domain of the Atm protein (UniProt.org). S2017T has not been characterized in the scientific literature and therefore, its effect on Atm protein function is unknown (PubMed, Jan 2025). |
Associated Drug Resistance | |
Category Variants Paths |
ATM mutant ATM S2017T |
Transcript | NM_000051.4 |
gDNA | chr11:g.108315866G>C |
cDNA | c.6050G>C |
Protein | p.S2017T |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_047426975.1 | chr11:g.108315866G>C | c.6050G>C | p.S2017T | RefSeq | GRCh38/hg38 |
XM_005271562.5 | chr11:g.108315866G>C | c.6050G>C | p.S2017T | RefSeq | GRCh38/hg38 |
XM_011542840.4 | chr11:g.108315866G>C | c.6050G>C | p.S2017T | RefSeq | GRCh38/hg38 |
XM_005271562.6 | chr11:g.108315866G>C | c.6050G>C | p.S2017T | RefSeq | GRCh38/hg38 |
XM_017017791.1 | chr11:g.108315866G>C | c.6050G>C | p.S2017T | RefSeq | GRCh38/hg38 |
NM_001351834.1 | chr11:g.108315866G>C | c.6050G>C | p.S2017T | RefSeq | GRCh38/hg38 |
NM_001351834.2 | chr11:g.108315866G>C | c.6050G>C | p.S2017T | RefSeq | GRCh38/hg38 |
XM_047426976.1 | chr11:g.108315866G>C | c.6050G>C | p.S2017T | RefSeq | GRCh38/hg38 |
XM_017017790.2 | chr11:g.108315866G>C | c.6050G>C | p.S2017T | RefSeq | GRCh38/hg38 |
NM_000051.4 | chr11:g.108315866G>C | c.6050G>C | p.S2017T | RefSeq | GRCh38/hg38 |
XM_011542840.3 | chr11:g.108315866G>C | c.6050G>C | p.S2017T | RefSeq | GRCh38/hg38 |
XM_006718843.4 | chr11:g.108315866G>C | c.6050G>C | p.S2017T | RefSeq | GRCh38/hg38 |
XM_011542843.3 | chr11:g.108315866G>C | c.6050G>C | p.S2017T | RefSeq | GRCh38/hg38 |
XM_006718843.5 | chr11:g.108315866G>C | c.6050G>C | p.S2017T | RefSeq | GRCh38/hg38 |
NM_000051.3 | chr11:g.108315866G>C | c.6050G>C | p.S2017T | RefSeq | GRCh38/hg38 |
XM_017017790.3 | chr11:g.108315866G>C | c.6050G>C | p.S2017T | RefSeq | GRCh38/hg38 |
XM_011542843.2 | chr11:g.108315866G>C | c.6050G>C | p.S2017T | RefSeq | GRCh38/hg38 |
XM_017017789.2 | chr11:g.108315866G>C | c.6050G>C | p.S2017T | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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