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Gene | FGFR3 |
Variant | G375C |
Impact List | missense |
Protein Effect | gain of function - predicted |
Gene Variant Descriptions | FGFR3 G375C lies within the extracellular domain of the Fgfr3 protein (UniProt.org). G375C results in a similar dimer formation to wild-type, but demonstrates increased Fgfr3 autophosphorylation in the absence of ligand in culture (PMID: 22529939), and therefore, is predicted to lead to a gain of Fgfr3 protein function. |
Associated Drug Resistance | |
Category Variants Paths |
FGFR3 mutant FGFR3 act mut FGFR3 G375C |
Transcript | NM_000142.5 |
gDNA | chr4:g.1804377G>T |
cDNA | c.1123G>T |
Protein | p.G375C |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_011513420 | chr4:g.1804377G>T | c.1123G>T | p.G375C | RefSeq | GRCh38/hg38 |
XM_006713872 | chr4:g.1804377G>T | c.1123G>T | p.G375C | RefSeq | GRCh38/hg38 |
NM_001354810.1 | chr4:g.1804377G>T | c.1123G>T | p.G375C | RefSeq | GRCh38/hg38 |
XM_047449823.1 | chr4:g.1804377G>T | c.1123G>T | p.G375C | RefSeq | GRCh38/hg38 |
NM_000142.4 | chr4:g.1804377G>T | c.1123G>T | p.G375C | RefSeq | GRCh38/hg38 |
XM_011513422 | chr4:g.1804377G>T | c.1123G>T | p.G375C | RefSeq | GRCh38/hg38 |
XM_006713873 | chr4:g.1804377G>T | c.1123G>T | p.G375C | RefSeq | GRCh38/hg38 |
XM_047449822.1 | chr4:g.1804377G>T | c.1123G>T | p.G375C | RefSeq | GRCh38/hg38 |
NM_001354810.2 | chr4:g.1804377G>T | c.1123G>T | p.G375C | RefSeq | GRCh38/hg38 |
XM_011513422.2 | chr4:g.1804377G>T | c.1123G>T | p.G375C | RefSeq | GRCh38/hg38 |
NM_000142.5 | chr4:g.1804377G>T | c.1123G>T | p.G375C | RefSeq | GRCh38/hg38 |
XM_006713873.1 | chr4:g.1804377G>T | c.1123G>T | p.G375C | RefSeq | GRCh38/hg38 |
XM_047449824.1 | chr4:g.1804377G>T | c.1123G>T | p.G375C | RefSeq | GRCh38/hg38 |
XM_011513420.1 | chr4:g.1804377G>T | c.1123G>T | p.G375C | RefSeq | GRCh38/hg38 |
NM_001354809.1 | chr4:g.1804377G>T | c.1123G>T | p.G375C | RefSeq | GRCh38/hg38 |
NM_000142 | chr4:g.1804377G>T | c.1123G>T | p.G375C | RefSeq | GRCh38/hg38 |
XM_011513422.1 | chr4:g.1804377G>T | c.1123G>T | p.G375C | RefSeq | GRCh38/hg38 |
XM_011513420.2 | chr4:g.1804377G>T | c.1123G>T | p.G375C | RefSeq | GRCh38/hg38 |
NM_001354809.2 | chr4:g.1804377G>T | c.1123G>T | p.G375C | RefSeq | GRCh38/hg38 |
XM_006713873.2 | chr4:g.1804377G>T | c.1123G>T | p.G375C | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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