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Gene | FGFR2 |
Variant | G583V |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | FGFR2 G583V lies within the protein kinase domain of the Fgfr2 protein (UniProt.org). G583V has been identified in sequencing studies (PMID: 22980975, PMID: 26960398), 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 G583V |
Transcript | NM_000141.5 |
gDNA | chr10:g.121496647C>A |
cDNA | c.1748G>T |
Protein | p.G583V |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001144918.1 | chr10:g.121485491C>A | c.1748G>T | p.G583V | RefSeq | GRCh38/hg38 |
NM_000141.5 | chr10:g.121496647C>A | c.1748G>T | p.G583V | RefSeq | GRCh38/hg38 |
NM_000141.4 | chr10:g.121496647C>A | c.1748G>T | p.G583V | RefSeq | GRCh38/hg38 |
NM_001144918 | chr10:g.121485491C>A | c.1748G>T | p.G583V | RefSeq | GRCh38/hg38 |
NM_000141 | chr10:g.121496647C>A | c.1748G>T | p.G583V | RefSeq | GRCh38/hg38 |
NM_001144918.2 | chr10:g.121485491C>A | c.1748G>T | p.G583V | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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