Gene Variant Detail

Contact

Missing content? – Request curation!

Request curation for specific Genes, Variants, or PubMed publications.

Have questions, comments, or suggestions? - Let us know!

Email us at : ckbsupport@genomenon.com

Gene FBXW7
Variant R224L
Impact List missense
Protein Effect unknown
Gene Variant Descriptions FBXW7 R224L does not lie within any known functional domains of the Fbxw7 protein (UniProt.org). R224L has not been characterized in the scientific literature and therefore, its effect on Fbxw7 protein function is unknown (PubMed, Oct 2024).
Associated Drug Resistance
Category Variants Paths

FBXW7 mutant FBXW7 R224L

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.

Transcript NM_033632.3
gDNA chr4:g.152346985C>A
cDNA c.671G>T
Protein p.R224L
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_033632.3 chr4:g.152346985C>A c.671G>T p.R224L RefSeq GRCh38/hg38
XM_011532085.2 chr4:g.152346985C>A c.671G>T p.R224L RefSeq GRCh38/hg38
XM_047415900.1 chr4:g.152346985C>A c.671G>T p.R224L RefSeq GRCh38/hg38
XM_047415897.1 chr4:g.152346985C>A c.671G>T p.R224L RefSeq GRCh38/hg38
XM_024454122.1 chr4:g.152346985C>A c.671G>T p.R224L RefSeq GRCh38/hg38
XM_024454123.1 chr4:g.152346985C>A c.671G>T p.R224L RefSeq GRCh38/hg38
XM_024454121.1 chr4:g.152346985C>A c.671G>T p.R224L RefSeq GRCh38/hg38
NM_001349798.1 chr4:g.152346985C>A c.671G>T p.R224L RefSeq GRCh38/hg38
XM_011532084.3 chr4:g.152346985C>A c.671G>T p.R224L RefSeq GRCh38/hg38
XM_047415899.1 chr4:g.152346985C>A c.671G>T p.R224L RefSeq GRCh38/hg38
XM_011532085.3 chr4:g.152346985C>A c.671G>T p.R224L RefSeq GRCh38/hg38
XM_011532084.2 chr4:g.152346985C>A c.671G>T p.R224L RefSeq GRCh38/hg38
XM_024454124.1 chr4:g.152346985C>A c.671G>T p.R224L RefSeq GRCh38/hg38
NM_001349798.2 chr4:g.152346985C>A c.671G>T p.R224L RefSeq GRCh38/hg38
XM_047415901.1 chr4:g.152346985C>A c.671G>T p.R224L RefSeq GRCh38/hg38
XM_024454123.2 chr4:g.152346985C>A c.671G>T p.R224L RefSeq GRCh38/hg38
NM_033632.3 chr4:g.152346985C>A c.671G>T p.R224L RefSeq GRCh38/hg38
XM_047415898.1 chr4:g.152346985C>A c.671G>T p.R224L 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.
  • 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.

Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References