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| Gene | FGFR1 |
| Variant | C379R |
| Impact List | missense |
| Protein Effect | gain of function |
| Gene Variant Descriptions | FGFR1 C379R (corresponds to C381R in the canonical isoform) lies within the transmembrane domain of the Fgfr1 protein (PMID: 26272615). C379R results in a gain of function, as demonstrated by constitutive Fgfr1 activity in a luciferase assay and increased Erk1/2 phosphorylation in cell culture (PMID: 26272615). |
| Associated Drug Resistance | |
| Category Variants Paths |
FGFR1 mutant FGFR1 act mut FGFR1 C379R |
| Transcript | NM_015850.4 |
| gDNA | chr8:g.38419676A>G |
| cDNA | c.1135T>C |
| Protein | p.C379R |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| XM_017013223 | chr8:g.38419676A>G | c.1135T>C | p.C379R | RefSeq | GRCh38/hg38 |
| XM_017013224 | chr8:g.38419676A>G | c.1135T>C | p.C379R | RefSeq | GRCh38/hg38 |
| NM_001174065.1 | chr8:g.38419676A>G | c.1135T>C | p.C379R | RefSeq | GRCh38/hg38 |
| XM_006716307 | chr8:g.38419676A>G | c.1135T>C | p.C379R | RefSeq | GRCh38/hg38 |
| XM_017013224.2 | chr8:g.38419676A>G | c.1135T>C | p.C379R | RefSeq | GRCh38/hg38 |
| NM_015850.4 | chr8:g.38419676A>G | c.1135T>C | p.C379R | RefSeq | GRCh38/hg38 |
| NM_001354367.1 | chr8:g.38419676A>G | c.1135T>C | p.C379R | RefSeq | GRCh38/hg38 |
| NM_001174065 | chr8:g.38419676A>G | c.1135T>C | p.C379R | RefSeq | GRCh38/hg38 |
| NM_001354369.1 | chr8:g.38419676A>G | c.1135T>C | p.C379R | RefSeq | GRCh38/hg38 |
| XM_006716307.2 | chr8:g.38419676A>G | c.1135T>C | p.C379R | RefSeq | GRCh38/hg38 |
| NM_001354367.2 | chr8:g.38419676A>G | c.1135T>C | p.C379R | RefSeq | GRCh38/hg38 |
| NM_001410922.1 | chr8:g.38419676A>G | c.1135T>C | p.C379R | RefSeq | GRCh38/hg38 |
| NM_001174065.2 | chr8:g.38419676A>G | c.1135T>C | p.C379R | RefSeq | GRCh38/hg38 |
| NM_015850 | chr8:g.38419676A>G | c.1135T>C | p.C379R | RefSeq | GRCh38/hg38 |
| XM_006716307.1 | chr8:g.38419676A>G | c.1135T>C | p.C379R | RefSeq | GRCh38/hg38 |
| NM_001354369.2 | chr8:g.38419676A>G | c.1135T>C | p.C379R | RefSeq | GRCh38/hg38 |
| XM_017013225.3 | chr8:g.38419676A>G | c.1135T>C | p.C379R | RefSeq | GRCh38/hg38 |
| NM_015850.3 | chr8:g.38419676A>G | c.1135T>C | p.C379R | RefSeq | GRCh38/hg38 |
| XM_017013225 | chr8:g.38419676A>G | c.1135T>C | p.C379R | RefSeq | GRCh38/hg38 |
| XM_047421569.1 | chr8:g.38419676A>G | c.1135T>C | p.C379R | RefSeq | GRCh38/hg38 |
| XM_017013225.2 | chr8:g.38419676A>G | c.1135T>C | p.C379R | RefSeq | GRCh38/hg38 |
| XM_006716306 | chr8:g.38419676A>G | c.1135T>C | p.C379R | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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