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Gene | FGFR3 |
Variant | S249C |
Impact List | missense |
Protein Effect | gain of function |
Gene Variant Descriptions | FGFR3 S249C lies within the linker region between IgD2 and IgD3 of the Fgfr3 protein (PMID: 19381019). S249C results in stabilized homodimer formation and constitutive Fgfr3 phosphorylation in vitro (PMID: 17384684), ligand-independent cell proliferation in culture (PMID: 19381019, PMID: 29533785), increased Akt signaling (PMID: 31316618), a growth advantage relative to wild-type Fgfr3 in a competition assay, and increased transformation activity in cultured cells (PMID: 34272467). |
Associated Drug Resistance | Y |
Category Variants Paths |
FGFR3 mutant FGFR3 act mut FGFR3 S249C |
Transcript | NM_000142.5 |
gDNA | chr4:g.1801841C>G |
cDNA | c.746C>G |
Protein | p.S249C |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001163213 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
NM_001163213.2 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_011513420.1 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_006713870 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_047449822.1 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_006713868.2 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_006713871.1 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_006713871 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_006713869 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
NM_001163213.1 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
NM_022965.3 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
NM_001354809.2 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
NM_001354810.2 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_011513420.2 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_006713870.1 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_006713873.2 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_006713871.2 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
NM_022965.4 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_006713868 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
NM_000142 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_011513422.1 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_006713873.1 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
NM_001354809.1 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_011513422.2 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_047449823.1 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_011513420 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
NM_000142.4 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_047449820.1 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
NM_000142.5 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_006713869.1 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_006713873 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_006713870.2 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_006713868.1 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_006713872 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_006713869.2 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_011513422 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_047449821.1 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
NM_022965 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
XM_047449824.1 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |
NM_001354810.1 | chr4:g.1801841C>G | c.746C>G | p.S249C | RefSeq | GRCh38/hg38 |