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| Gene | ATM |
| Variant | R2227C |
| Impact List | missense |
| Protein Effect | loss of function - predicted |
| Gene Variant Descriptions | ATM R2227C lies within the FAT domain of the Atm protein (UniProt.org). R2227C results in reduced Atm protein expression, and increased radiosensitivity of cultured cells (PMID: 18634022), and therefore, is predicted to lead to a loss of Atm protein function. |
| Associated Drug Resistance | |
| Category Variants Paths |
ATM mutant ATM inact mut ATM R2227C |
| Transcript | NM_000051.4 |
| gDNA | chr11:g.108325416C>T |
| cDNA | c.6679C>T |
| Protein | p.R2227C |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| XM_011542843.3 | chr11:g.108325416C>T | c.6679C>T | p.R2227C | RefSeq | GRCh38/hg38 |
| NM_000051.4 | chr11:g.108325416C>T | c.6679C>T | p.R2227C | RefSeq | GRCh38/hg38 |
| XM_005271562.6 | chr11:g.108325416C>T | c.6679C>T | p.R2227C | RefSeq | GRCh38/hg38 |
| XM_047426976.1 | chr11:g.108325416C>T | c.6679C>T | p.R2227C | RefSeq | GRCh38/hg38 |
| XM_011542840.4 | chr11:g.108325416C>T | c.6679C>T | p.R2227C | RefSeq | GRCh38/hg38 |
| XM_006718843.5 | chr11:g.108325416C>T | c.6679C>T | p.R2227C | RefSeq | GRCh38/hg38 |
| NM_001351834.2 | chr11:g.108325416C>T | c.6679C>T | p.R2227C | RefSeq | GRCh38/hg38 |
| XM_047426975.1 | chr11:g.108325416C>T | c.6679C>T | p.R2227C | RefSeq | GRCh38/hg38 |
| XM_017017790.3 | chr11:g.108325416C>T | c.6679C>T | p.R2227C | RefSeq | GRCh38/hg38 |
| Molecular Profile | Protein Effect | Treatment Approaches |
|---|---|---|
| ATM R2227C | loss of function - predicted | Olaparib |