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Gene ATM
Variant S1135_K1192del
Impact List deletion
Protein Effect unknown
Gene Variant Descriptions ATM S1135_K1192del results in the deletion of 58 amino acids of the Atm protein from amino acids 1135 to 1192 (UniProt.org). S1135_K1192del is associated with loss of Atm expression and phosphorylation in patient samples (PMID: 36555667, PMID: 32748564), but has not been biochemically characterized and therefore, its effect on Atm protein function is unknown (PubMed, Jun 2024).
Associated Drug Resistance
Category Variants Paths

ATM mutant ATM S1135_K1192del

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Transcript NM_000051.4
gDNA chr11:g.108280995_108281168del174
cDNA c.3403_3576del174
Protein p.S1135_K1192del58
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_005271562.5 chr11:g.108280995_108281168del174 c.3403_3576del174 p.S1135_K1192del RefSeq GRCh38/hg38
NM_001351834.1 chr11:g.108280995_108281168del174 c.3403_3576del174 p.S1135_K1192del RefSeq GRCh38/hg38
XM_047426975.1 chr11:g.108280995_108281168del174 c.3403_3576del174 p.S1135_K1192del58 RefSeq GRCh38/hg38
XM_006718845.3 chr11:g.108330353_108331548del1196 c.3403_3576del1196 p.W1135_V1192del58 RefSeq GRCh38/hg38
XM_017017790.2 chr11:g.108280995_108281168del174 c.3403_3576del174 p.S1135_K1192del RefSeq GRCh38/hg38
XM_011542842.4 chr11:g.108281160_108282874del1715 c.3403_3576del1715 p.V1135_F1192del58 RefSeq GRCh38/hg38
XM_006718843.4 chr11:g.108280995_108281168del174 c.3403_3576del174 p.S1135_K1192del RefSeq GRCh38/hg38
XM_006718843.5 chr11:g.108280995_108281168del174 c.3403_3576del174 p.S1135_K1192del58 RefSeq GRCh38/hg38
XM_047426979.1 chr11:g.108281160_108282874del1715 c.3403_3576del1715 p.V1135_F1192del58 RefSeq GRCh38/hg38
XM_047426978.1 chr11:g.108281160_108282874del1715 c.3403_3576del1715 p.V1135_F1192del58 RefSeq GRCh38/hg38
NM_000051.4 chr11:g.108280995_108281168del174 c.3403_3576del174 p.S1135_K1192del58 RefSeq GRCh38/hg38
XM_011542840.4 chr11:g.108280995_108281168del174 c.3403_3576del174 p.S1135_K1192del58 RefSeq GRCh38/hg38
XM_017017790.3 chr11:g.108280995_108281168del174 c.3403_3576del174 p.S1135_K1192del58 RefSeq GRCh38/hg38
XM_011542844.4 chr11:g.108292629_108293321del693 c.3403_3576del693 p.I1135_D1192del58 RefSeq GRCh38/hg38
XM_047426976.1 chr11:g.108280995_108281168del174 c.3403_3576del174 p.S1135_K1192del58 RefSeq GRCh38/hg38
XM_005271562.6 chr11:g.108280995_108281168del174 c.3403_3576del174 p.S1135_K1192del58 RefSeq GRCh38/hg38
NM_000051.3 chr11:g.108280995_108281168del174 c.3403_3576del174 p.S1135_K1192del RefSeq GRCh38/hg38
NM_001351834.2 chr11:g.108280995_108281168del174 c.3403_3576del174 p.S1135_K1192del58 RefSeq GRCh38/hg38
XM_011542840.3 chr11:g.108280995_108281168del174 c.3403_3576del174 p.S1135_K1192del RefSeq GRCh38/hg38
XM_047426977.1 chr11:g.108281160_108282874del1715 c.3403_3576del1715 p.V1135_F1192del58 RefSeq GRCh38/hg38
XM_047426981.1 chr11:g.108280995_108281168del174 c.3403_3576del174 p.S1135_K1192del58 RefSeq GRCh38/hg38
XM_011542843.3 chr11:g.108280995_108281168del174 c.3403_3576del174 p.S1135_K1192del58 RefSeq GRCh38/hg38
XM_017017789.2 chr11:g.108280995_108281168del174 c.3403_3576del174 p.S1135_K1192del 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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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References