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Gene FGFR2
Variant E777K
Impact List missense
Protein Effect unknown
Gene Variant Descriptions FGFR2 E777K lies within the cytoplasmic domain of the Fgfr2 protein (UniProt.org). E777K has been identified in sequencing studies (PMID: 29107334), 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 E777K

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Transcript NM_000141.5
gDNA chr10:g.121479994C>T
cDNA c.2329G>A
Protein p.E777K
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_000141 chr10:g.121479994C>T c.2329G>A p.E777K RefSeq GRCh38/hg38
NM_000141.4 chr10:g.121479994C>T c.2329G>A p.E777K RefSeq GRCh38/hg38
NM_000141.5 chr10:g.121479994C>T c.2329G>A p.E777K 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

  • Generally, the default sort order for tables is set to be first column ascending; however, specific tables may set a different default sort order.
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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References