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| Gene | FGFR3 |
| Variant | S433C |
| Impact List | missense |
| Protein Effect | unknown |
| Gene Variant Descriptions | FGFR3 S433C lies within the cytoplasmic domain of the Fgfr3 protein (UniProt.org). S433C has been identified in the scientific literature (PMID: 17344920), but has not been biochemically characterized and therefore, its effect on Fgfr3 protein function is unknown (PubMed, Aug 2025). |
| Associated Drug Resistance | |
| Category Variants Paths |
FGFR3 mutant FGFR3 S433C |
| Transcript | NM_000142.5 |
| gDNA | chr4:g.1804855C>G |
| cDNA | c.1298C>G |
| Protein | p.S433C |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| XM_006713873 | chr4:g.1804855C>G | c.1298C>G | p.S433C | RefSeq | GRCh38/hg38 |
| NM_000142.5 | chr4:g.1804855C>G | c.1298C>G | p.S433C | RefSeq | GRCh38/hg38 |
| XM_006713873.2 | chr4:g.1804855C>G | c.1298C>G | p.S433C | RefSeq | GRCh38/hg38 |
| XM_006713870.1 | chr4:g.1804846C>G | c.1298C>G | p.S433C | RefSeq | GRCh38/hg38 |
| XM_006713870 | chr4:g.1804846C>G | c.1298C>G | p.S433C | RefSeq | GRCh38/hg38 |
| XM_011513422.1 | chr4:g.1804851A>T | c.1297A>T | p.S433C | RefSeq | GRCh38/hg38 |
| NM_001354809.1 | chr4:g.1804851A>T | c.1297A>T | p.S433C | RefSeq | GRCh38/hg38 |
| XM_006713870.2 | chr4:g.1804846C>G | c.1298C>G | p.S433C | RefSeq | GRCh38/hg38 |
| XM_047449823.1 | chr4:g.1804855C>G | c.1298C>G | p.S433C | RefSeq | GRCh38/hg38 |
| XM_047449824.1 | chr4:g.1804855C>G | c.1298C>G | p.S433C | RefSeq | GRCh38/hg38 |
| XM_006713872 | chr4:g.1804851A>T | c.1297A>T | p.S433C | RefSeq | GRCh38/hg38 |
| NM_001354810.1 | chr4:g.1804851A>T | c.1297A>T | p.S433C | RefSeq | GRCh38/hg38 |
| XM_047449821.1 | chr4:g.1804846C>G | c.1298C>G | p.S433C | RefSeq | GRCh38/hg38 |
| XM_047449822.1 | chr4:g.1804851A>T | c.1297A>T | p.S433C | RefSeq | GRCh38/hg38 |
| XM_011513422 | chr4:g.1804851A>T | c.1297A>T | p.S433C | RefSeq | GRCh38/hg38 |
| XM_011513422.2 | chr4:g.1804851A>T | c.1297A>T | p.S433C | RefSeq | GRCh38/hg38 |
| NM_000142 | chr4:g.1804855C>G | c.1298C>G | p.S433C | RefSeq | GRCh38/hg38 |
| NM_000142.4 | chr4:g.1804855C>G | c.1298C>G | p.S433C | RefSeq | GRCh38/hg38 |
| XM_006713873.1 | chr4:g.1804855C>G | c.1298C>G | p.S433C | RefSeq | GRCh38/hg38 |
| NM_001354810.2 | chr4:g.1804851A>T | c.1297A>T | p.S433C | RefSeq | GRCh38/hg38 |
| NM_001354809.2 | chr4:g.1804851A>T | c.1297A>T | p.S433C | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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