ATM R337X
Gene Variant Detail

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Gene ATM
Variant R337X
Impact List missense
Protein Effect unknown
Gene Variant Descriptions ATM R337X indicates any ATM missense mutation that results in replacement of the arginine (R) at amino acid 337 by a different amino acid.
Associated Drug Resistance
Category Variants Paths

ATM mutant ATM R337X

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Transcript NM_000051.4
gDNA chr11:g.108247071_108247073
cDNA c.1009_1011
Protein p.R337
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_047426975.1 chr11:g.108247071_108247073 c.1009_1011 p.R337 RefSeq GRCh38/hg38
XM_047426976.1 chr11:g.108247071_108247073 c.1009_1011 p.R337 RefSeq GRCh38/hg38
XM_017017790.3 chr11:g.108247071_108247073 c.1009_1011 p.R337 RefSeq GRCh38/hg38
XM_006718843.5 chr11:g.108247071_108247073 c.1009_1011 p.R337 RefSeq GRCh38/hg38
XM_011542840.4 chr11:g.108247071_108247073 c.1009_1011 p.R337 RefSeq GRCh38/hg38
XM_005271562.6 chr11:g.108247071_108247073 c.1009_1011 p.R337 RefSeq GRCh38/hg38
XM_011542843.3 chr11:g.108247071_108247073 c.1009_1011 p.R337 RefSeq GRCh38/hg38
XM_047426981.1 chr11:g.108247071_108247073 c.1009_1011 p.R337 RefSeq GRCh38/hg38
NM_001351834.2 chr11:g.108247071_108247073 c.1009_1011 p.R337 RefSeq GRCh38/hg38
NM_000051.4 chr11:g.108247071_108247073 c.1009_1011 p.R337 RefSeq GRCh38/hg38

Filtering

  • Case insensitive filtering will display rows if any text in any cell matches the filter term
  • 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

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