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| Gene | FGFR2 |
| Variant | S372F |
| Impact List | missense |
| Protein Effect | unknown |
| Gene Variant Descriptions | FGFR2 S372F lies within the extracellular domain of the Fgfr2 protein (Uniprot.org). S372F has been identified in sequencing studies (PMID: 27892470), 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 S372F |
| Transcript | NM_000141.5 |
| gDNA | chr10:g.121515289G>A |
| cDNA | c.1115C>T |
| Protein | p.S372F |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_000141 | chr10:g.121515289G>A | c.1115C>T | p.S372F | RefSeq | GRCh38/hg38 |
| NM_001320658 | chr10:g.121515289G>A | c.1115C>T | p.S372F | RefSeq | GRCh38/hg38 |
| NM_001320658.1 | chr10:g.121515289G>A | c.1115C>T | p.S372F | RefSeq | GRCh38/hg38 |
| NM_000141.4 | chr10:g.121515289G>A | c.1115C>T | p.S372F | RefSeq | GRCh38/hg38 |
| NM_000141.5 | chr10:g.121515289G>A | c.1115C>T | p.S372F | RefSeq | GRCh38/hg38 |
| NM_001320658.2 | chr10:g.121515289G>A | c.1115C>T | p.S372F | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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