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Gene | ATM |
Variant | F2827C |
Impact List | missense |
Protein Effect | loss of function |
Gene Variant Descriptions | ATM F2827C lies within the PI3K/PI4K domain of the Atm protein (UniProt.org). F2827C results in decreased protein expression, reduced phosphorylation of Atm and downstream targets, and failure to from foci in response to irradiation in culture (PMID: 19431188). |
Associated Drug Resistance | |
Category Variants Paths |
ATM mutant ATM inact mut ATM F2827C |
Transcript | NM_000051.4 |
gDNA | chr11:g.108345804T>G |
cDNA | c.8480T>G |
Protein | p.F2827C |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_017017790.3 | chr11:g.108345804T>G | c.8480T>G | p.F2827C | RefSeq | GRCh38/hg38 |
XM_047426976.1 | chr11:g.108345804T>G | c.8480T>G | p.F2827C | RefSeq | GRCh38/hg38 |
NM_000051.3 | chr11:g.108345804T>G | c.8480T>G | p.F2827C | RefSeq | GRCh38/hg38 |
XM_006718843.4 | chr11:g.108345804T>G | c.8480T>G | p.F2827C | RefSeq | GRCh38/hg38 |
XM_005271562 | chr11:g.108345804T>G | c.8480T>G | p.F2827C | RefSeq | GRCh38/hg38 |
XM_017017789.2 | chr11:g.108345804T>G | c.8480T>G | p.F2827C | RefSeq | GRCh38/hg38 |
XM_011542843 | chr11:g.108345804T>G | c.8480T>G | p.F2827C | RefSeq | GRCh38/hg38 |
XM_005271562.6 | chr11:g.108345804T>G | c.8480T>G | p.F2827C | RefSeq | GRCh38/hg38 |
NM_000051 | chr11:g.108345804T>G | c.8480T>G | p.F2827C | RefSeq | GRCh38/hg38 |
XM_006718843 | chr11:g.108345804T>G | c.8480T>G | p.F2827C | RefSeq | GRCh38/hg38 |
XM_006718843.5 | chr11:g.108345804T>G | c.8480T>G | p.F2827C | RefSeq | GRCh38/hg38 |
XM_017017789 | chr11:g.108345804T>G | c.8480T>G | p.F2827C | RefSeq | GRCh38/hg38 |
XM_005271562.5 | chr11:g.108345804T>G | c.8480T>G | p.F2827C | RefSeq | GRCh38/hg38 |
XM_011542840.4 | chr11:g.108345804T>G | c.8480T>G | p.F2827C | RefSeq | GRCh38/hg38 |
XM_047426975.1 | chr11:g.108345804T>G | c.8480T>G | p.F2827C | RefSeq | GRCh38/hg38 |
XM_011542840 | chr11:g.108345804T>G | c.8480T>G | p.F2827C | RefSeq | GRCh38/hg38 |
XM_011542843.2 | chr11:g.108345804T>G | c.8480T>G | p.F2827C | RefSeq | GRCh38/hg38 |
NM_001351834.1 | chr11:g.108345804T>G | c.8480T>G | p.F2827C | RefSeq | GRCh38/hg38 |
NM_001351834.2 | chr11:g.108345804T>G | c.8480T>G | p.F2827C | RefSeq | GRCh38/hg38 |
NM_000051.4 | chr11:g.108345804T>G | c.8480T>G | p.F2827C | RefSeq | GRCh38/hg38 |
XM_011542840.3 | chr11:g.108345804T>G | c.8480T>G | p.F2827C | RefSeq | GRCh38/hg38 |
XM_005271561 | chr11:g.108345804T>G | c.8480T>G | p.F2827C | RefSeq | GRCh38/hg38 |
XM_011542843.3 | chr11:g.108345804T>G | c.8480T>G | p.F2827C | RefSeq | GRCh38/hg38 |
XM_017017790 | chr11:g.108345804T>G | c.8480T>G | p.F2827C | RefSeq | GRCh38/hg38 |
XM_017017790.2 | chr11:g.108345804T>G | c.8480T>G | p.F2827C | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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