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Gene | ATM |
Variant | P2353T |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | ATM P2353T lies within the FAT domain of the Atm protein (UniProt.org). P2353T has been identified in sequencing studies (PMID: 22810696), but has not been biochemically characterized and therefore, its effect on Atm protein function is unknown (PubMed, Oct 2024). |
Associated Drug Resistance | |
Category Variants Paths |
ATM mutant ATM P2353T |
Transcript | NM_000051.4 |
gDNA | chr11:g.108327726C>A |
cDNA | c.7057C>A |
Protein | p.P2353T |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_006718843.4 | chr11:g.108327726C>A | c.7057C>A | p.P2353T | RefSeq | GRCh38/hg38 |
XM_017017789 | chr11:g.108327726C>A | c.7057C>A | p.P2353T | RefSeq | GRCh38/hg38 |
NM_001351834.2 | chr11:g.108327726C>A | c.7057C>A | p.P2353T | RefSeq | GRCh38/hg38 |
XM_005271561 | chr11:g.108327726C>A | c.7057C>A | p.P2353T | RefSeq | GRCh38/hg38 |
NM_000051.4 | chr11:g.108327726C>A | c.7057C>A | p.P2353T | RefSeq | GRCh38/hg38 |
XM_011542843 | chr11:g.108327726C>A | c.7057C>A | p.P2353T | RefSeq | GRCh38/hg38 |
XM_011542840.3 | chr11:g.108327726C>A | c.7057C>A | p.P2353T | RefSeq | GRCh38/hg38 |
XM_011542843.3 | chr11:g.108327726C>A | c.7057C>A | p.P2353T | RefSeq | GRCh38/hg38 |
XM_005271562.5 | chr11:g.108327726C>A | c.7057C>A | p.P2353T | RefSeq | GRCh38/hg38 |
XM_017017790 | chr11:g.108327726C>A | c.7057C>A | p.P2353T | RefSeq | GRCh38/hg38 |
XM_047426976.1 | chr11:g.108327726C>A | c.7057C>A | p.P2353T | RefSeq | GRCh38/hg38 |
XM_011542840 | chr11:g.108327726C>A | c.7057C>A | p.P2353T | RefSeq | GRCh38/hg38 |
XM_011542843.2 | chr11:g.108327726C>A | c.7057C>A | p.P2353T | RefSeq | GRCh38/hg38 |
NM_000051.3 | chr11:g.108327726C>A | c.7057C>A | p.P2353T | RefSeq | GRCh38/hg38 |
XM_005271562 | chr11:g.108327726C>A | c.7057C>A | p.P2353T | RefSeq | GRCh38/hg38 |
NM_000051 | chr11:g.108327726C>A | c.7057C>A | p.P2353T | RefSeq | GRCh38/hg38 |
XM_006718843.5 | chr11:g.108327726C>A | c.7057C>A | p.P2353T | RefSeq | GRCh38/hg38 |
XM_017017790.2 | chr11:g.108327726C>A | c.7057C>A | p.P2353T | RefSeq | GRCh38/hg38 |
XM_005271562.6 | chr11:g.108327726C>A | c.7057C>A | p.P2353T | RefSeq | GRCh38/hg38 |
NM_001351834.1 | chr11:g.108327726C>A | c.7057C>A | p.P2353T | RefSeq | GRCh38/hg38 |
XM_047426975.1 | chr11:g.108327726C>A | c.7057C>A | p.P2353T | RefSeq | GRCh38/hg38 |
XM_006718843 | chr11:g.108327726C>A | c.7057C>A | p.P2353T | RefSeq | GRCh38/hg38 |
XM_011542840.4 | chr11:g.108327726C>A | c.7057C>A | p.P2353T | RefSeq | GRCh38/hg38 |
XM_017017789.2 | chr11:g.108327726C>A | c.7057C>A | p.P2353T | RefSeq | GRCh38/hg38 |
XM_017017790.3 | chr11:g.108327726C>A | c.7057C>A | p.P2353T | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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