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| Gene | FGFR2 |
| Variant | D479N |
| Impact List | missense |
| Protein Effect | unknown |
| Gene Variant Descriptions | FGFR2 D479N lies within the cytoplasmic domain of the Fgfr2 protein (UniProt.org). D479N has been identified in sequencing studies (PMID: 25035393), 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 D479N |
| Transcript | NM_000141.5 |
| gDNA | chr10:g.121503794C>T |
| cDNA | c.1435G>A |
| Protein | p.D479N |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_000141.5 | chr10:g.121503794C>T | c.1435G>A | p.D479N | RefSeq | GRCh38/hg38 |
| NM_000141.4 | chr10:g.121503794C>T | c.1435G>A | p.D479N | RefSeq | GRCh38/hg38 |
| NM_000141 | chr10:g.121503794C>T | c.1435G>A | p.D479N | RefSeq | GRCh38/hg38 |
| Molecular Profile | Protein Effect | Treatment Approaches |
|---|---|---|
| FGFR2 D479N | unknown |