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Gene | CSF3R |
Variant | D771fs |
Impact List | frameshift |
Protein Effect | gain of function |
Gene Variant Descriptions | CSF3R D771fs results in a change in the amino acid sequence of the Csf3r protein beginning at aa 771 of 836, likely resulting in premature truncation of the functional protein (UniProt.org). D771fs results in increased cell surface Csf3r expression, impaired receptor internalization, hypersensitivity to G-CSF stimulation, elevated Stat5 activation, and is transforming in cell culture (PMID: 24403076, PMID: 28439110). |
Associated Drug Resistance | |
Category Variants Paths |
CSF3R mutant CSF3R act mut CSF3R D771fs |
Transcript | NM_000760.4 |
gDNA | chr1:g.(36466557_36466558) |
cDNA | c.(2311_2310) |
Protein | p.D771fs |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_000760 | chr1:g.(36466557_36466558) | c.(2311_2310) | p.D771fs | RefSeq | GRCh38/hg38 |
NM_000760.4 | chr1:g.(36466557_36466558) | c.(2311_2310) | p.D771fs | RefSeq | GRCh38/hg38 |
NM_000760.3 | chr1:g.(36466557_36466558) | c.(2311_2310) | p.D771fs | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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