Gene Variant Detail

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Gene ATM
Variant R1882*
Impact List nonsense
Protein Effect loss of function - predicted
Gene Variant Descriptions ATM R1882* results in a premature truncation of the Atm protein at amino acid 1882 of 3056 (UniProt.org). R1882* has not been characterized, however, based on the effects of other truncation mutations downstream of R1882 (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 R1882*

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Transcript NM_000051.3
gDNA chr11:g.108304822C>T
cDNA c.5644C>T
Protein p.R1882*
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001351834.1 chr11:g.108304822C>T c.5644C>T p.R1882* RefSeq GRCh38/hg38
XM_017017790.2 chr11:g.108304822C>T c.5644C>T p.R1882* RefSeq GRCh38/hg38
XM_017017791.1 chr11:g.108304822C>T c.5644C>T p.R1882* RefSeq GRCh38/hg38
XM_017017789.2 chr11:g.108304822C>T c.5644C>T p.R1882* RefSeq GRCh38/hg38
XM_005271562.5 chr11:g.108304822C>T c.5644C>T p.R1882* RefSeq GRCh38/hg38
NM_000051.3 chr11:g.108304822C>T c.5644C>T p.R1882* RefSeq GRCh38/hg38
XM_011542840.3 chr11:g.108304822C>T c.5644C>T p.R1882* RefSeq GRCh38/hg38
XM_011542843.2 chr11:g.108304822C>T c.5644C>T p.R1882* RefSeq GRCh38/hg38
XM_006718843.4 chr11:g.108304822C>T c.5644C>T p.R1882* RefSeq GRCh38/hg38

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  • Simple literal full or partial string matches
  • Separate multiple filter terms with a spaces, order doesn't matter (a b c and c b a are equivalent )
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  • Use quotes to match a longer phrase which contains spaces "mtor c1483f"

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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References