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Gene | ATM |
Variant | F1683V |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | ATM F1683V does not lie within any known functional domains of the Atm protein (UniProt.org). F1683V has not been characterized in the scientific literature and therefore, its effect on Atm protein function is unknown (PubMed, Oct 2024). |
Associated Drug Resistance | |
Category Variants Paths |
ATM mutant ATM F1683V |
Transcript | NM_000051.4 |
gDNA | chr11:g.108299755T>G |
cDNA | c.5047T>G |
Protein | p.F1683V |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_005271561 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
XM_005271562.5 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
XM_017017792.2 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
XM_011542843.3 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
NM_001351834.1 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
NM_000051 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
XM_017017790.2 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
XM_017017791.1 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
NM_000051.3 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
XM_005271562 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
NM_000051.4 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
XM_017017792 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
XM_017017790.3 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
XM_047426976.1 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
XM_017017789.2 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
XM_006718843 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
XM_017017790 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
XM_011542840 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
XM_006718843.5 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
XM_047426975.1 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
XM_011542843 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
XM_017017789 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
XM_005271562.6 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
NM_001351834.2 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
XM_011542843.2 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
XM_017017791 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
XM_006718843.4 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
XM_011542840.4 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
XM_011542840.3 | chr11:g.108299755T>G | c.5047T>G | p.F1683V | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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