Missing content? – Request curation!
Request curation for specific Genes, Variants, or PubMed publications.
Have questions, comments, or suggestions? - Let us know!
Email us at : ckbsupport@genomenon.com
| Gene | FGFR2 |
| Variant | G583V |
| Impact List | missense |
| Protein Effect | unknown |
| Gene Variant Descriptions | FGFR2 G583V lies within the protein kinase domain of the Fgfr2 protein (UniProt.org). G583V has been identified in sequencing studies (PMID: 22980975, PMID: 26960398), but has not been biochemically characterized and therefore, its effect on Fgfr2 protein function is unknown (PubMed, Nov 2025). |
| Associated Drug Resistance | |
| Category Variants Paths |
FGFR2 mutant FGFR2 G583V |
| Transcript | NM_000141.5 |
| gDNA | chr10:g.121496647C>A |
| cDNA | c.1748G>T |
| Protein | p.G583V |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_000141 | chr10:g.121496647C>A | c.1748G>T | p.G583V | RefSeq | GRCh38/hg38 |
| NM_000141.4 | chr10:g.121496647C>A | c.1748G>T | p.G583V | RefSeq | GRCh38/hg38 |
| NM_000141.5 | chr10:g.121496647C>A | c.1748G>T | p.G583V | RefSeq | GRCh38/hg38 |
| NM_001144918.2 | chr10:g.121485491C>A | c.1748G>T | p.G583V | RefSeq | GRCh38/hg38 |
| NM_001144918.1 | chr10:g.121485491C>A | c.1748G>T | p.G583V | RefSeq | GRCh38/hg38 |
| NM_001144918 | chr10:g.121485491C>A | c.1748G>T | p.G583V | RefSeq | GRCh38/hg38 |
| Molecular Profile | Protein Effect | Treatment Approaches |
|---|---|---|
| FGFR2 G583V | unknown |