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Gene | FGFR2 |
Variant | S587C |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | FGFR2 S587C lies within the protein kinase domain of the Fgfr2 protein (UniProt.org). S587C has been identified in the scientific literature (PMID: 23000897), but has not been biochemically characterized and therefore, its effect on Fgfr2 protein function is unknown (PubMed, Nov 2024). |
Associated Drug Resistance | |
Category Variants Paths |
FGFR2 mutant FGFR2 S587C |
Transcript | NM_000141.5 |
gDNA | chr10:g.121496635G>C |
cDNA | c.1760C>G |
Protein | p.S587C |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001144916 | chr10:g.121485484_121485485delCGinsAC | c.1760_1761delCGinsGT | p.S587C | RefSeq | GRCh38/hg38 |
NM_001144916.1 | chr10:g.121485484_121485485delCGinsGT | c.1760_1761delCGinsGT | p.S587C | RefSeq | GRCh38/hg38 |
NM_001144916.2 | chr10:g.121485484_121485485delCGinsGT | c.1760_1761delCGinsGT | p.S587C | RefSeq | GRCh38/hg38 |
NM_000141 | chr10:g.121496635G>C | c.1760C>G | p.S587C | RefSeq | GRCh38/hg38 |
NM_000141.4 | chr10:g.121496635G>C | c.1760C>G | p.S587C | RefSeq | GRCh38/hg38 |
NM_000141.5 | chr10:g.121496635G>C | c.1760C>G | p.S587C | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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