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| Gene | FGFR2 |
| Variant | D530N |
| Impact List | missense |
| Protein Effect | loss of function |
| Gene Variant Descriptions | FGFR2 D530N lies within the protein kinase domain of the Fgfr2 protein (UniProt.org). D530N confers a loss of function on the Fgfr2 protein, as demonstrated by decreased protein kinase activity and reduced downstream MAPK signaling pathway activation, and decreased proliferation compared to wild-type Fgfr2 in cell culture (PMID: 19147536). |
| Associated Drug Resistance | |
| Category Variants Paths |
FGFR2 mutant FGFR2 inact mut FGFR2 D530N |
| Transcript | NM_000141.5 |
| gDNA | chr10:g.121498579C>T |
| cDNA | c.1588G>A |
| Protein | p.D530N |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| XM_017015923 | chr10:g.121496591C>T | c.1588G>A | p.D530N | RefSeq | GRCh38/hg38 |
| XM_017015924.3 | chr10:g.121488101C>T | c.1588G>A | p.D530N | RefSeq | GRCh38/hg38 |
| NM_001320654.1 | chr10:g.121483727C>T | c.1588G>A | p.D530N | RefSeq | GRCh38/hg38 |
| XM_017015924.2 | chr10:g.121488101C>T | c.1588G>A | p.D530N | RefSeq | GRCh38/hg38 |
| NM_000141.4 | chr10:g.121498579C>T | c.1588G>A | p.D530N | RefSeq | GRCh38/hg38 |
| XM_024447889.1 | chr10:g.121496591C>T | c.1588G>A | p.D530N | RefSeq | GRCh38/hg38 |
| XM_024447889.2 | chr10:g.121496591C>T | c.1588G>A | p.D530N | RefSeq | GRCh38/hg38 |
| NM_001320654 | chr10:g.121483727C>T | c.1588G>A | p.D530N | RefSeq | GRCh38/hg38 |
| XM_017015924 | chr10:g.121488101C>T | c.1588G>A | p.D530N | RefSeq | GRCh38/hg38 |
| NM_001320654.2 | chr10:g.121483727C>T | c.1588G>A | p.D530N | RefSeq | GRCh38/hg38 |
| NM_000141.5 | chr10:g.121498579C>T | c.1588G>A | p.D530N | RefSeq | GRCh38/hg38 |
| NM_000141 | chr10:g.121498579C>T | c.1588G>A | p.D530N | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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