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Gene | ATM |
Variant | P2974L |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | ATM P2974L lies within the PI3K/PI4K domain of the Atm protein (UniProt.org). P2974L confers a loss of function on the Atm protein as demonstrated by reduced phosphorylation of Atm, Chk2, and Tp53, increased DNA damage, and reduced homologous recombination repair activity in culture (PMID: 31160347). |
Associated Drug Resistance | |
Category Variants Paths |
ATM mutant ATM inact mut ATM P2974L |
Transcript | NM_000051.4 |
gDNA | chr11:g.108365152C>T |
cDNA | c.8921C>T |
Protein | p.P2974L |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_047426976.1 | chr11:g.108365152C>T | c.8921C>T | p.P2974L | RefSeq | GRCh38/hg38 |
XM_005271562.5 | chr11:g.108365152C>T | c.8921C>T | p.P2974L | RefSeq | GRCh38/hg38 |
XM_017017790.2 | chr11:g.108365152C>T | c.8921C>T | p.P2974L | RefSeq | GRCh38/hg38 |
XM_011542840 | chr11:g.108365152C>T | c.8921C>T | p.P2974L | RefSeq | GRCh38/hg38 |
NM_001351834.1 | chr11:g.108365152C>T | c.8921C>T | p.P2974L | RefSeq | GRCh38/hg38 |
XM_011542840.3 | chr11:g.108365152C>T | c.8921C>T | p.P2974L | RefSeq | GRCh38/hg38 |
NM_001351834.2 | chr11:g.108365152C>T | c.8921C>T | p.P2974L | RefSeq | GRCh38/hg38 |
XM_017017789.2 | chr11:g.108365152C>T | c.8921C>T | p.P2974L | RefSeq | GRCh38/hg38 |
XM_017017790.3 | chr11:g.108365152C>T | c.8921C>T | p.P2974L | RefSeq | GRCh38/hg38 |
XM_011542840.4 | chr11:g.108365152C>T | c.8921C>T | p.P2974L | RefSeq | GRCh38/hg38 |
XM_006718843.5 | chr11:g.108365152C>T | c.8921C>T | p.P2974L | RefSeq | GRCh38/hg38 |
XM_005271562.6 | chr11:g.108365152C>T | c.8921C>T | p.P2974L | RefSeq | GRCh38/hg38 |
XM_017017789 | chr11:g.108365152C>T | c.8921C>T | p.P2974L | RefSeq | GRCh38/hg38 |
NM_000051.3 | chr11:g.108365152C>T | c.8921C>T | p.P2974L | RefSeq | GRCh38/hg38 |
XM_006718843.4 | chr11:g.108365152C>T | c.8921C>T | p.P2974L | RefSeq | GRCh38/hg38 |
NM_000051 | chr11:g.108365152C>T | c.8921C>T | p.P2974L | RefSeq | GRCh38/hg38 |
XM_005271561 | chr11:g.108365152C>T | c.8921C>T | p.P2974L | RefSeq | GRCh38/hg38 |
XM_047426975.1 | chr11:g.108365152C>T | c.8921C>T | p.P2974L | RefSeq | GRCh38/hg38 |
XM_006718843 | chr11:g.108365152C>T | c.8921C>T | p.P2974L | RefSeq | GRCh38/hg38 |
XM_017017790 | chr11:g.108365152C>T | c.8921C>T | p.P2974L | RefSeq | GRCh38/hg38 |
NM_000051.4 | chr11:g.108365152C>T | c.8921C>T | p.P2974L | RefSeq | GRCh38/hg38 |
XM_005271562 | chr11:g.108365152C>T | c.8921C>T | p.P2974L | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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