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Gene | ATM |
Variant | N81Tfs*20 |
Impact List | frameshift |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | ATM N81Tfs*20 indicates a shift in the reading frame starting at amino acid 81 and terminating 20 residues downstream causing a premature truncation of the 3056 amino acid Atm protein (UniProt.org). N81Tfs*20 has not been characterized, however, due to the effects of other truncation mutations downstream of N81 (PMID: 16603769), is predicted to lead to a loss of Atm protein function. |
Associated Drug Resistance | |
Category Variants Paths |
ATM mutant ATM inact mut ATM N81Tfs*20 |
Transcript | NM_000051.4 |
gDNA | chr11:g.108229233_108229234insCAAA |
cDNA | c.241_242insCAAA |
Protein | p.N81Tfs*20 |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_017017790.2 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
XM_005271562.6 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
XM_047426975.1 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
XM_011542844.4 | chr11:g.(108250750_108250812) | c.(241_303) | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
XM_011542842.4 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
XM_047426977.1 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
NM_001351836.2 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
XM_006718843.5 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
XM_011542840.4 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
XM_047426979.1 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
XM_017017789.2 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
XM_011542842.3 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
NM_001351836.1 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
XM_047426976.1 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
NM_000051.3 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
XM_005271562.5 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
NM_000051.4 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
XM_011542840.3 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
NM_001351834.2 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
NM_001351835.1 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
NM_001351835.2 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
XM_006718843.4 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
NM_001351834.1 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
XM_011542843.2 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
XM_047426978.1 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
XM_047426981.1 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
XM_017017792.2 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
XM_011542843.3 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
XM_017017791.1 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
XM_017017790.3 | chr11:g.108229233_108229234insCAAA | c.241_242insCAAA | p.N81Tfs*20 | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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