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Gene | ATM |
Variant | T1743I |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | ATM T1743I does not lie within any known functional domains of the Atm protein (UniProt.org). T1743I results in decreased protein expression and reduced phosphorylation of Atm and downstream targets in response to irradiation in culture (PMID: 19431188). |
Associated Drug Resistance | |
Category Variants Paths |
ATM mutant ATM inact mut ATM T1743I |
Transcript | NM_000051.4 |
gDNA | chr11:g.108301698C>T |
cDNA | c.5228C>T |
Protein | p.T1743I |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_006718843 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
XM_017017790 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
XM_017017789 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
NM_001351834.2 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
XM_011542840.3 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
XM_017017791 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
XM_011542843.2 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
XM_017017792.2 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
XM_011542843 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
XM_017017790.2 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
XM_006718843.5 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
NM_001351834.1 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
NM_000051.3 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
XM_017017790.3 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
XM_005271562.5 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
XM_047426976.1 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
XM_011542840.4 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
XM_017017789.2 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
XM_005271562 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
XM_011542840 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
XM_005271561 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
XM_017017791.1 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
XM_011542843.3 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
NM_000051.4 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
XM_006718843.4 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
XM_017017792 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
XM_047426975.1 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
XM_005271562.6 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
NM_000051 | chr11:g.108301698C>T | c.5228C>T | p.T1743I | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
ATM T1743I | loss of function | Olaparib |