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Gene FGFR2
Variant S354C
Impact List missense
Protein Effect gain of function
Gene Variant Descriptions FGFR2 S354C lies within the Ig-like C2-type domain 3 of the Fgfr2 protein (UniProt.org). S354C confers a gain of function to the Fgfr2 protein, as demonstrated by increased transactivation of Runx2, increased autophosphorylation, and increased Erk1/2 phosphorylation, as compared to wild-type in in vitro assays (PMID: 23913723).
Associated Drug Resistance
Category Variants Paths

FGFR2 mutant FGFR2 act mut FGFR2 S354C

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Transcript NM_000141.5
gDNA chr10:g.121517342G>C
cDNA c.1061C>G
Protein p.S354C
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_000141.5 chr10:g.121517342G>C c.1061C>G p.S354C RefSeq GRCh38/hg38
NM_001320658.1 chr10:g.121517342G>C c.1061C>G p.S354C RefSeq GRCh38/hg38
XM_017015925.3 chr10:g.121503874G>C c.1061C>G p.S354C RefSeq GRCh38/hg38
NM_001320658 chr10:g.121517342G>C c.1061C>G p.S354C RefSeq GRCh38/hg38
NM_001320658.2 chr10:g.121517342G>C c.1061C>G p.S354C RefSeq GRCh38/hg38
XM_017015925.2 chr10:g.121503874G>C c.1061C>G p.S354C RefSeq GRCh38/hg38
XM_017015925 chr10:g.121503874G>C c.1061C>G p.S354C RefSeq GRCh38/hg38
NM_000141 chr10:g.121517342G>C c.1061C>G p.S354C RefSeq GRCh38/hg38
NM_000141.4 chr10:g.121517342G>C c.1061C>G p.S354C RefSeq GRCh38/hg38

Filtering

  • Case insensitive filtering will display rows if any text in any cell matches the filter term
  • Use simple literal full or partial string matches
  • Separate multiple filter terms with a space. Any order may be used (i. e. a b c and c b a are equivalent )
  • Filtering will only apply to rows that are already loaded on the page. Filtering has no impact on query parameters.
  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

Sorting

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Molecular Profile Protein Effect Treatment Approaches
FGFR2 S354C gain of function FGFR Inhibitor (Pan) FGFR2 Inhibitor