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Gene FGFR2
Variant P781*
Impact List nonsense
Protein Effect gain of function - predicted
Gene Variant Descriptions FGFR2 P781* results in a premature truncation of the Fgfr2 protein at amino acid 781 of 821 (UniProt.org). P781* is predicted to lead to a gain of Fgfr2 protein function as a corresponding mouse variant (P686*) promotes colony formation in cell culture and leads to tumor formation in a mouse model (PMID: 35948633).
Associated Drug Resistance
Category Variants Paths

FGFR2 mutant FGFR2 act mut FGFR2 P781*

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Transcript NM_000141.5
gDNA chr10:g.121479980_121479982delCCTinsTAA
cDNA c.2341_2343delCCTinsTAA
Protein p.P781*
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_000141.5 chr10:g.121479980_121479982delCCTinsTAA c.2341_2343delCCTinsTAA p.P781* RefSeq GRCh38/hg38
NM_000141.4 chr10:g.121479980_121479982delCCTinsTAA c.2341_2343delCCTinsTAA p.P781* 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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Clinical Trial Phase Therapies Title Recruitment Status Covered Countries Other Countries