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Gene ATM
Variant T2333Nfs*40
Impact List frameshift
Protein Effect loss of function - predicted
Gene Variant Descriptions ATM T2333Nfs*40 indicates a shift in the reading frame starting at amino acid 2333 and terminating 40 residues downstream causing a premature truncation of the 3056 amino acid Atm protein (UniProt.org). T2333Nfs*40 has not been characterized, however, due to the effects of other truncation mutations downstream of T2333 (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 T2333fs ATM T2333Nfs*40

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Transcript NM_000051.4
gDNA chr11:g.108327666dupA
cDNA c.6997dupA
Protein p.T2333Nfs*40
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_006718843.5 chr11:g.108327666dupA c.6997dupA p.T2333Nfs*40 RefSeq GRCh38/hg38
NM_000051.4 chr11:g.108327666dupA c.6997dupA p.T2333Nfs*40 RefSeq GRCh38/hg38
XM_017017789.2 chr11:g.108327666dupA c.6997dupA p.T2333Nfs*40 RefSeq GRCh38/hg38
XM_011542843.3 chr11:g.108327666dupA c.6997dupA p.T2333Nfs*40 RefSeq GRCh38/hg38
XM_006718843.4 chr11:g.108327666dupA c.6997dupA p.T2333Nfs*40 RefSeq GRCh38/hg38
XM_017017790.3 chr11:g.108327666dupA c.6997dupA p.T2333Nfs*40 RefSeq GRCh38/hg38
XM_011542843 chr11:g.108327666dupA c.6997dupA p.T2333Nfs*40 RefSeq GRCh38/hg38
XM_006718843 chr11:g.108327666dupA c.6997dupA p.T2333Nfs*40 RefSeq GRCh38/hg38
XM_005271562.5 chr11:g.108327666dupA c.6997dupA p.T2333Nfs*40 RefSeq GRCh38/hg38
NM_001351834.1 chr11:g.108327666dupA c.6997dupA p.T2333Nfs*40 RefSeq GRCh38/hg38
XM_017017789 chr11:g.108327666dupA c.6997dupA p.T2333Nfs*40 RefSeq GRCh38/hg38
NM_000051 chr11:g.108327666dupA c.6997dupA p.T2333Nfs*40 RefSeq GRCh38/hg38
XM_005271561 chr11:g.108327666dupA c.6997dupA p.T2333Nfs*40 RefSeq GRCh38/hg38
XM_011542840 chr11:g.108327666dupA c.6997dupA p.T2333Nfs*40 RefSeq GRCh38/hg38
NM_001351834.2 chr11:g.108327666dupA c.6997dupA p.T2333Nfs*40 RefSeq GRCh38/hg38
XM_047426976.1 chr11:g.108327666dupA c.6997dupA p.T2333Nfs*40 RefSeq GRCh38/hg38
XM_017017790.2 chr11:g.108327666dupA c.6997dupA p.T2333Nfs*40 RefSeq GRCh38/hg38
XM_005271562 chr11:g.108327666dupA c.6997dupA p.T2333Nfs*40 RefSeq GRCh38/hg38
XM_011542843.2 chr11:g.108327666dupA c.6997dupA p.T2333Nfs*40 RefSeq GRCh38/hg38
XM_011542840.4 chr11:g.108327666dupA c.6997dupA p.T2333Nfs*40 RefSeq GRCh38/hg38
XM_011542840.3 chr11:g.108327666dupA c.6997dupA p.T2333Nfs*40 RefSeq GRCh38/hg38
NM_000051.3 chr11:g.108327666dupA c.6997dupA p.T2333Nfs*40 RefSeq GRCh38/hg38
XM_047426975.1 chr11:g.108327666dupA c.6997dupA p.T2333Nfs*40 RefSeq GRCh38/hg38
XM_005271562.6 chr11:g.108327666dupA c.6997dupA p.T2333Nfs*40 RefSeq GRCh38/hg38
XM_017017790 chr11:g.108327666dupA c.6997dupA p.T2333Nfs*40 RefSeq GRCh38/hg38

Filtering

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  • Use simple literal full or partial string matches
  • Separate multiple filter terms with a space. Any order may be used (i. e. a b c and c b a are equivalent )
  • Filtering will only apply to rows that are already loaded on the page. Filtering has no impact on query parameters.
  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

Sorting

  • Generally, the default sort order for tables is set to be first column ascending; however, specific tables may set a different default sort order.
  • Click on any column header arrows to sort by that column
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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References
ATM T2333Nfs*40 pancreatic ductal adenocarcinoma no benefit Fluorouracil + Oxaliplatin + Veliparib Case Reports/Case Series Actionable In a Phase I/II trial, Veliparib (ABT-888) in combination with Adrucil (fluorouracil) and Eloxatin (oxaliplatin) did not result in a clinical response in a patient with metastatic pancreatic ductal adenocarcinoma harboring ATM T2333Nfs*40 (reported as c.6997dupA) (PMID: 32669374; NCT01489865). 32669374