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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 |
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 |
---|---|---|---|---|---|
NM_000051.4 | 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_005271562.6 | 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_006718843.5 | 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 |
XM_017017790.3 | 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_047426975.1 | 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 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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