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| Gene | FGFR2 |
| Variant | N211I |
| Impact List | missense |
| Protein Effect | unknown |
| Gene Variant Descriptions | FGFR2 N211I lies within Ig-like C2-type domain 2 of the Fgfr2 protein (UniProt.org). N211I has been identified in sequencing studies (PMID: 18552176), but has not been biochemically characterized and therefore, its effect on Fgfr2 protein function is unknown (PubMed, Dec 2025). |
| Associated Drug Resistance | |
| Category Variants Paths |
FGFR2 mutant FGFR2 N211I |
| Transcript | NM_000141.5 |
| gDNA | chr10:g.121538708T>A |
| cDNA | c.632A>T |
| Protein | p.N211I |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_001144917.1 | chr10:g.121538708T>A | c.632A>T | p.N211I | RefSeq | GRCh38/hg38 |
| NM_001320654.2 | chr10:g.121503913T>A | c.632A>T | p.N211I | RefSeq | GRCh38/hg38 |
| NM_001144913.1 | chr10:g.121538708T>A | c.632A>T | p.N211I | RefSeq | GRCh38/hg38 |
| NM_001144917 | chr10:g.121538708T>A | c.632A>T | p.N211I | RefSeq | GRCh38/hg38 |
| NM_001144914.1 | chr10:g.121538708T>A | c.632A>T | p.N211I | RefSeq | GRCh38/hg38 |
| NM_001320658 | chr10:g.121538708T>A | c.632A>T | p.N211I | RefSeq | GRCh38/hg38 |
| NM_001144914.1 | chr10:g.121538708T>A | c.632A>T | p.N211I | RefSeq | GRCh38/hg38 |
| NM_022970.3 | chr10:g.121538708T>A | c.632A>T | p.N211I | RefSeq | GRCh38/hg38 |
| NM_001320658.2 | chr10:g.121538708T>A | c.632A>T | p.N211I | RefSeq | GRCh38/hg38 |
| NM_022970 | chr10:g.121538708T>A | c.632A>T | p.N211I | RefSeq | GRCh38/hg38 |
| NM_001144913.1 | chr10:g.121538708T>A | c.632A>T | p.N211I | RefSeq | GRCh38/hg38 |
| NM_000141.4 | chr10:g.121538708T>A | c.632A>T | p.N211I | RefSeq | GRCh38/hg38 |
| NM_001144914 | chr10:g.121538708T>A | c.632A>T | p.N211I | RefSeq | GRCh38/hg38 |
| NM_001144917.2 | chr10:g.121538708T>A | c.632A>T | p.N211I | RefSeq | GRCh38/hg38 |
| NM_001320654 | chr10:g.121503913T>A | c.632A>T | p.N211I | RefSeq | GRCh38/hg38 |
| NM_001320654.1 | chr10:g.121503913T>A | c.632A>T | p.N211I | RefSeq | GRCh38/hg38 |
| NM_000141.5 | chr10:g.121538708T>A | c.632A>T | p.N211I | RefSeq | GRCh38/hg38 |
| NM_000141 | chr10:g.121538708T>A | c.632A>T | p.N211I | RefSeq | GRCh38/hg38 |
| NM_001144913 | chr10:g.121538708T>A | c.632A>T | p.N211I | RefSeq | GRCh38/hg38 |
| NM_022970.4 | chr10:g.121538708T>A | c.632A>T | p.N211I | RefSeq | GRCh38/hg38 |
| NM_001320658.1 | chr10:g.121538708T>A | c.632A>T | p.N211I | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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