FBXW7 S668Vfs*39 - Gene Variant Detail

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Gene FBXW7
Variant S668Vfs*39
Impact List frameshift
Protein Effect unknown
Gene Variant Descriptions FBXW7 S668Vfs*39 indicates a shift in the reading frame starting at amino acid 668 and terminating 39 residues downstream causing a premature truncation of the 707 amino acid Fbxw7 protein (UniProt.org). S668Vfs*39 has been identified in the scientific literature (J Thorac Oncol 13:10, 2018 (suppl; abstr S524)), but has not been biochemically characterized and therefore, its effect on Fbxw7 protein function is unknown (PubMed, Apr 2025).
Associated Drug Resistance
Category Variants Paths

FBXW7 mutant FBXW7 S668fs FBXW7 S668Vfs*39

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Transcript NM_033632.3
gDNA chr4:g.152323003delT
cDNA c.2002delA
Protein p.S668Vfs*39
Source Database RefSeq
Genome Build 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.
  • Click on any column header arrows to sort by that column
  • Hold down the Shift key and click multiple columns to sort by more than one column. Be sure to set ascending or descending order for a given column before moving on to the next column.