Gene Variant Detail

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Gene ATM
Variant A1309T
Impact List missense
Protein Effect unknown
Gene Variant Descriptions ATM A1309T does not lie within any known functional domains of the Atm protein (UniProt.org). A1309T has been identified in the scientific literature (PMID: 24886963, PMID: 31552911, PMID: 12697903), but has not been biochemically characterized and therefore, its effect on Atm protein function is unknown (PubMed, Dec 2023).
Associated Drug Resistance
Category Variants Paths

ATM mutant ATM A1309T

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Transcript NM_000051.4
gDNA chr11:g.108284405G>A
cDNA c.3925G>A
Protein p.A1309T
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_017017791 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
XM_017017792.2 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
NM_000051.3 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
XM_005271562.5 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
XM_011542840.3 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
NM_001351834.1 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
XM_005271562.6 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
NM_000051 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
XM_006718843.5 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
XM_047426975.1 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
XM_017017791.1 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
XM_047426981.1 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
XM_011542843 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
NM_001351834.2 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
XM_017017792 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
XM_005271561 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
XM_017017790.2 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
XM_011542840.4 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
XM_017017789 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
XM_006718843 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
XM_017017790.3 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
XM_047426976.1 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
XM_006718843.4 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
XM_017017790 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
XM_005271562 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
XM_011542843.3 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
XM_017017789.2 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
XM_011542843.2 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
XM_011542840 chr11:g.108284405G>A c.3925G>A p.A1309T RefSeq GRCh38/hg38
NM_000051.4 chr11:g.108284405G>A c.3925G>A p.A1309T 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

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  • 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