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| Gene | FGFR3 |
| Variant | G372C |
| Impact List | missense |
| Protein Effect | gain of function |
| Gene Variant Descriptions | FGFR3 G372C (corresponds to G370C in the canonical isoform) lies within the extracellular domain of the Fgfr3 protein (UniProt.org). G372C confers a gain of function on Fgfr3, as indicated by ligand-independent phosphorylation and dimerization of Fgfr3, and activation of MAPK pathway in cell culture (PMID: 16841094, PMID: 12009017). |
| Associated Drug Resistance | |
| Category Variants Paths |
FGFR3 mutant FGFR3 act mut FGFR3 G372C |
| Transcript | NM_022965.4 |
| gDNA | chr4:g.1805392G>T |
| cDNA | c.1114G>T |
| Protein | p.G372C |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_022965 | chr4:g.1805392G>T | c.1114G>T | p.G372C | RefSeq | GRCh38/hg38 |
| NM_001163213.1 | chr4:g.1804362G>T | c.1114G>T | p.G372C | RefSeq | GRCh38/hg38 |
| NM_022965.3 | chr4:g.1805392G>T | c.1114G>T | p.G372C | RefSeq | GRCh38/hg38 |
| XM_047449821.1 | chr4:g.1804362G>T | c.1114G>T | p.G372C | RefSeq | GRCh38/hg38 |
| NM_001163213 | chr4:g.1804362G>T | c.1114G>T | p.G372C | RefSeq | GRCh38/hg38 |
| XM_006713871 | chr4:g.1804362G>T | c.1114G>T | p.G372C | RefSeq | GRCh38/hg38 |
| XM_006713869.2 | chr4:g.1804362G>T | c.1114G>T | p.G372C | RefSeq | GRCh38/hg38 |
| XM_006713868 | chr4:g.1804362G>T | c.1114G>T | p.G372C | RefSeq | GRCh38/hg38 |
| XM_006713870.2 | chr4:g.1804362G>T | c.1114G>T | p.G372C | RefSeq | GRCh38/hg38 |
| XM_006713868.1 | chr4:g.1804362G>T | c.1114G>T | p.G372C | RefSeq | GRCh38/hg38 |
| XM_006713871.1 | chr4:g.1804362G>T | c.1114G>T | p.G372C | RefSeq | GRCh38/hg38 |
| XM_006713868.2 | chr4:g.1804362G>T | c.1114G>T | p.G372C | RefSeq | GRCh38/hg38 |
| NM_001163213.2 | chr4:g.1804362G>T | c.1114G>T | p.G372C | RefSeq | GRCh38/hg38 |
| XM_047449820.1 | chr4:g.1804362G>T | c.1114G>T | p.G372C | RefSeq | GRCh38/hg38 |
| XM_006713870.1 | chr4:g.1804362G>T | c.1114G>T | p.G372C | RefSeq | GRCh38/hg38 |
| XM_006713871.2 | chr4:g.1804362G>T | c.1114G>T | p.G372C | RefSeq | GRCh38/hg38 |
| XM_006713869 | chr4:g.1804362G>T | c.1114G>T | p.G372C | RefSeq | GRCh38/hg38 |
| NM_022965.4 | chr4:g.1805392G>T | c.1114G>T | p.G372C | RefSeq | GRCh38/hg38 |
| XM_006713870 | chr4:g.1804362G>T | c.1114G>T | p.G372C | RefSeq | GRCh38/hg38 |
| XM_006713869.1 | chr4:g.1804362G>T | c.1114G>T | p.G372C | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
|---|---|---|---|---|---|---|---|
| FGFR3 G372C | Advanced Solid Tumor | sensitive | Vofatamab | Preclinical - Cell culture | Actionable | In a preclinical study, Vofatamab (B-701) inhibited ligand-dependent proliferation in cells expressing FGFR3 G372C (PMID: 19381019). | 19381019 |