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Gene | ATM |
Variant | K2756* |
Impact List | nonsense |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | ATM K2756* results in a premature truncation of the Atm protein at amino acid 2756 of 3056 (UniProt.org). Due to the loss of the FATC domain, R2756* is predicted to lead to a loss of Atm protein function (PMID: 16603769). |
Associated Drug Resistance | |
Category Variants Paths |
ATM mutant ATM inact mut ATM K2756* |
Transcript | NM_000051.3 |
gDNA | chr11:g.108335959A>T |
cDNA | c.8266A>T |
Protein | p.K2756* |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_011542843.2 | chr11:g.108335959A>T | c.8266A>T | p.K2756* | RefSeq | GRCh38/hg38 |
NM_000051 | chr11:g.108335959A>T | c.8266A>T | p.K2756* | RefSeq | GRCh38/hg38 |
XM_011542843 | chr11:g.108335959A>T | c.8266A>T | p.K2756* | RefSeq | GRCh38/hg38 |
XM_011542840 | chr11:g.108335959A>T | c.8266A>T | p.K2756* | RefSeq | GRCh38/hg38 |
XM_006718843 | chr11:g.108335959A>T | c.8266A>T | p.K2756* | RefSeq | GRCh38/hg38 |
XM_005271562.5 | chr11:g.108335959A>T | c.8266A>T | p.K2756* | RefSeq | GRCh38/hg38 |
XM_011542840.3 | chr11:g.108335959A>T | c.8266A>T | p.K2756* | RefSeq | GRCh38/hg38 |
NM_001351834.1 | chr11:g.108335959A>T | c.8266A>T | p.K2756* | RefSeq | GRCh38/hg38 |
XM_017017789 | chr11:g.108335959A>T | c.8266A>T | p.K2756* | RefSeq | GRCh38/hg38 |
XM_011542842.3 | chr11:g.108345755A>T | c.8266A>T | p.K2756* | RefSeq | GRCh38/hg38 |
XM_005271562 | chr11:g.108335959A>T | c.8266A>T | p.K2756* | RefSeq | GRCh38/hg38 |
XM_017017789.2 | chr11:g.108335959A>T | c.8266A>T | p.K2756* | RefSeq | GRCh38/hg38 |
XM_006718843.4 | chr11:g.108335959A>T | c.8266A>T | p.K2756* | RefSeq | GRCh38/hg38 |
XM_011542842 | chr11:g.108345755A>T | c.8266A>T | p.K2756* | RefSeq | GRCh38/hg38 |
XM_017017790.2 | chr11:g.108335959A>T | c.8266A>T | p.K2756* | RefSeq | GRCh38/hg38 |
NM_000051.3 | chr11:g.108335959A>T | c.8266A>T | p.K2756* | RefSeq | GRCh38/hg38 |
XM_005271561 | chr11:g.108335959A>T | c.8266A>T | p.K2756* | RefSeq | GRCh38/hg38 |
XM_017017790 | chr11:g.108335959A>T | c.8266A>T | p.K2756* | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
ATM K2756* | loss of function - predicted | Olaparib |