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Gene | ATM |
Variant | P2699L |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | ATM P2699L lies within the ATP-binding pocket of the Atm protein (PMID: 21993670). P2699L results in decreased protein expression and a loss of phosphorylation of Atm downstream targets in response to irradiation in culture (PMID: 19431188). |
Associated Drug Resistance | |
Category Variants Paths |
ATM mutant ATM inact mut ATM P2699L |
Transcript | NM_000051.4 |
gDNA | chr11:g.108335054C>T |
cDNA | c.8096C>T |
Protein | p.P2699L |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_011542843.2 | chr11:g.108335054C>T | c.8096C>T | p.P2699L | RefSeq | GRCh38/hg38 |
XM_011542843.3 | chr11:g.108335054C>T | c.8096C>T | p.P2699L | RefSeq | GRCh38/hg38 |
XM_017017789.2 | chr11:g.108335054C>T | c.8096C>T | p.P2699L | RefSeq | GRCh38/hg38 |
XM_011542840.3 | chr11:g.108335054C>T | c.8096C>T | p.P2699L | RefSeq | GRCh38/hg38 |
NM_000051.4 | chr11:g.108335054C>T | c.8096C>T | p.P2699L | RefSeq | GRCh38/hg38 |
XM_017017790.3 | chr11:g.108335054C>T | c.8096C>T | p.P2699L | RefSeq | GRCh38/hg38 |
NM_001351834.1 | chr11:g.108335054C>T | c.8096C>T | p.P2699L | RefSeq | GRCh38/hg38 |
XM_011542843 | chr11:g.108335054C>T | c.8096C>T | p.P2699L | RefSeq | GRCh38/hg38 |
XM_047426976.1 | chr11:g.108335054C>T | c.8096C>T | p.P2699L | RefSeq | GRCh38/hg38 |
XM_017017789 | chr11:g.108335054C>T | c.8096C>T | p.P2699L | RefSeq | GRCh38/hg38 |
XM_017017790.2 | chr11:g.108335054C>T | c.8096C>T | p.P2699L | RefSeq | GRCh38/hg38 |
NM_001351834.2 | chr11:g.108335054C>T | c.8096C>T | p.P2699L | RefSeq | GRCh38/hg38 |
XM_005271562 | chr11:g.108335054C>T | c.8096C>T | p.P2699L | RefSeq | GRCh38/hg38 |
XM_011542840 | chr11:g.108335054C>T | c.8096C>T | p.P2699L | RefSeq | GRCh38/hg38 |
XM_006718843 | chr11:g.108335054C>T | c.8096C>T | p.P2699L | RefSeq | GRCh38/hg38 |
NM_000051 | chr11:g.108335054C>T | c.8096C>T | p.P2699L | RefSeq | GRCh38/hg38 |
XM_005271561 | chr11:g.108335054C>T | c.8096C>T | p.P2699L | RefSeq | GRCh38/hg38 |
XM_006718843.4 | chr11:g.108335054C>T | c.8096C>T | p.P2699L | RefSeq | GRCh38/hg38 |
XM_005271562.6 | chr11:g.108335054C>T | c.8096C>T | p.P2699L | RefSeq | GRCh38/hg38 |
XM_006718843.5 | chr11:g.108335054C>T | c.8096C>T | p.P2699L | RefSeq | GRCh38/hg38 |
XM_005271562.5 | chr11:g.108335054C>T | c.8096C>T | p.P2699L | RefSeq | GRCh38/hg38 |
XM_017017790 | chr11:g.108335054C>T | c.8096C>T | p.P2699L | RefSeq | GRCh38/hg38 |
XM_047426975.1 | chr11:g.108335054C>T | c.8096C>T | p.P2699L | RefSeq | GRCh38/hg38 |
NM_000051.3 | chr11:g.108335054C>T | c.8096C>T | p.P2699L | RefSeq | GRCh38/hg38 |
XM_011542840.4 | chr11:g.108335054C>T | c.8096C>T | p.P2699L | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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