ATM S1691R - Gene Variant Detail

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Gene ATM
Variant S1691R
Impact List missense
Protein Effect no effect
Gene Variant Descriptions ATM S1691R does not lie within any known functional domains of the Atm protein (UniProt.org). S1691R results in Atm protein expression, phosphorylation of Atm and downstream targets, and foci formation in response to irradiation to similar levels as wild-type Atm in culture (PMID: 19431188).
Associated Drug Resistance
Category Variants Paths

ATM mutant ATM S1691R

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Transcript NM_000051.4
gDNA chr11:g.108299781T>G
cDNA c.5073T>G
Protein p.S1691R
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_017017791.1 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
XM_017017789.2 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
XM_017017790.3 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
XM_005271561 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
XM_017017792.2 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
XM_017017791 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
XM_011542843 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
XM_047426975.1 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
XM_011542845.2 chr11:g.108319985_108319986delTCinsAG c.5071_5072delTCinsAG p.S1691R RefSeq GRCh38/hg38
XM_006718843 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
XM_006718843.4 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
XM_011542840 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
XM_006718843.5 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
XM_011542845 chr11:g.108319985_108319986delTCinsAG c.5071_5072delTCinsAG p.S1691R RefSeq GRCh38/hg38
XM_005271562.6 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
NM_001351834.2 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
XM_017017792 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
NM_001351834.1 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
XM_005271562.5 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
XM_011542843.2 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
NM_000051.4 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
XM_011542843.3 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
XM_017017790 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
NM_000051.3 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
XM_011542840.3 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
XM_017017790.2 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
XM_011542840.4 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
XM_017017789 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
XM_047426976.1 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
XM_005271562 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38
NM_000051 chr11:g.108299781T>G c.5073T>G p.S1691R RefSeq GRCh38/hg38

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  • 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
  • Hold down the Shift key and click multiple columns to sort by more than one column. Be sure to set ascending or descending order for a given column before moving on to the next column.

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