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| Gene | ATM |
| Variant | V2716A |
| Impact List | missense |
| Protein Effect | loss of function |
| Gene Variant Descriptions | ATM V2716A lies within the PI3K/PI4K domain of the Atm protein (UniProt.org). V2716A confers a loss of function to the Atm protein as demonstrated by loss of kinase activity in an in vitro assay and cultured cells, and increased radiosensitivity and radiation-induced chromosome aberrations in cultured cells (PMID: 11805335). |
| Associated Drug Resistance | |
| Category Variants Paths |
ATM mutant ATM inact mut ATM V2716A |
| Transcript | NM_000051.4 |
| gDNA | chr11:g.108335105T>C |
| cDNA | c.8147T>C |
| Protein | p.V2716A |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| XM_011542843.3 | chr11:g.108335105T>C | c.8147T>C | p.V2716A | RefSeq | GRCh38/hg38 |
| XM_005271562.5 | chr11:g.108335105T>C | c.8147T>C | p.V2716A | RefSeq | GRCh38/hg38 |
| NM_000051.4 | chr11:g.108335105T>C | c.8147T>C | p.V2716A | RefSeq | GRCh38/hg38 |
| XM_011542840.4 | chr11:g.108335105T>C | c.8147T>C | p.V2716A | RefSeq | GRCh38/hg38 |
| XM_047426975.1 | chr11:g.108335105T>C | c.8147T>C | p.V2716A | RefSeq | GRCh38/hg38 |
| XM_011542840.3 | chr11:g.108335105T>C | c.8147T>C | p.V2716A | RefSeq | GRCh38/hg38 |
| XM_017017790.2 | chr11:g.108335105T>C | c.8147T>C | p.V2716A | RefSeq | GRCh38/hg38 |
| XM_011542843.2 | chr11:g.108335105T>C | c.8147T>C | p.V2716A | RefSeq | GRCh38/hg38 |
| XM_006718843.5 | chr11:g.108335105T>C | c.8147T>C | p.V2716A | RefSeq | GRCh38/hg38 |
| XM_017017790.3 | chr11:g.108335105T>C | c.8147T>C | p.V2716A | RefSeq | GRCh38/hg38 |
| NM_001351834.2 | chr11:g.108335105T>C | c.8147T>C | p.V2716A | RefSeq | GRCh38/hg38 |
| XM_047426976.1 | chr11:g.108335105T>C | c.8147T>C | p.V2716A | RefSeq | GRCh38/hg38 |
| XM_005271562.6 | chr11:g.108335105T>C | c.8147T>C | p.V2716A | RefSeq | GRCh38/hg38 |
| XM_006718843.4 | chr11:g.108335105T>C | c.8147T>C | p.V2716A | RefSeq | GRCh38/hg38 |
| NM_001351834.1 | chr11:g.108335105T>C | c.8147T>C | p.V2716A | RefSeq | GRCh38/hg38 |
| XM_017017789.2 | chr11:g.108335105T>C | c.8147T>C | p.V2716A | RefSeq | GRCh38/hg38 |
| NM_000051.3 | chr11:g.108335105T>C | c.8147T>C | p.V2716A | RefSeq | GRCh38/hg38 |
| Molecular Profile | Protein Effect | Treatment Approaches |
|---|---|---|
| ATM V2716A | loss of function | Olaparib |