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FBXW7 R479G - Gene Variant Detail

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Gene FBXW7
Variant R479G
Impact List missense
Protein Effect loss of function - predicted
Gene Variant Descriptions FBXW7 R479G lies within the WD repeat domain of the Fbxw7 protein (UniProt.org). R479G has not been characterized however, other R479 hotspot mutations inactivate Fbxw7, and therefore, R479G is predicted to lead to a loss of function (PMID: 17646409, PMID: 17575125, PMID: 22608923).
Associated Drug Resistance
Category Variants Paths

FBXW7 mutant FBXW7 inact mut FBXW7 R479G

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Transcript NM_033632.3
gDNA chr4:g.152326215G>C
cDNA c.1435C>G
Protein p.R479G
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001349798.2 chr4:g.152326215G>C c.1435C>G p.R479G RefSeq GRCh38/hg38
XM_024454124.1 chr4:g.152326215G>C c.1435C>G p.R479G RefSeq GRCh38/hg38
XM_011532085 chr4:g.152326215G>C c.1435C>G p.R479G RefSeq GRCh38/hg38
XM_017008362 chr4:g.152326215G>C c.1435C>G p.R479G RefSeq GRCh38/hg38
XM_024454121.1 chr4:g.152326215G>C c.1435C>G p.R479G RefSeq GRCh38/hg38
XM_024454122.1 chr4:g.152326215G>C c.1435C>G p.R479G RefSeq GRCh38/hg38
NM_033632.3 chr4:g.152326215G>C c.1435C>G p.R479G RefSeq GRCh38/hg38
XM_011532085.2 chr4:g.152326215G>C c.1435C>G p.R479G RefSeq GRCh38/hg38
XM_011532085.3 chr4:g.152326215G>C c.1435C>G p.R479G RefSeq GRCh38/hg38
XM_047415898.1 chr4:g.152326215G>C c.1435C>G p.R479G RefSeq GRCh38/hg38
NM_001349798.1 chr4:g.152326215G>C c.1435C>G p.R479G RefSeq GRCh38/hg38
XM_011532083 chr4:g.152326215G>C c.1435C>G p.R479G RefSeq GRCh38/hg38
NM_033632 chr4:g.152326215G>C c.1435C>G p.R479G RefSeq GRCh38/hg38
XM_047415897.1 chr4:g.152326215G>C c.1435C>G p.R479G RefSeq GRCh38/hg38
XM_047415900.1 chr4:g.152326215G>C c.1435C>G p.R479G RefSeq GRCh38/hg38
XM_047415901.1 chr4:g.152326215G>C c.1435C>G p.R479G RefSeq GRCh38/hg38
XM_047415899.1 chr4:g.152326215G>C c.1435C>G p.R479G RefSeq GRCh38/hg38
NM_033632.3 chr4:g.152326215G>C c.1435C>G p.R479G RefSeq GRCh38/hg38
XM_024454123.2 chr4:g.152326215G>C c.1435C>G p.R479G RefSeq GRCh38/hg38
XM_024454123.1 chr4:g.152326215G>C c.1435C>G p.R479G RefSeq GRCh38/hg38
XM_011532084 chr4:g.152326215G>C c.1435C>G p.R479G RefSeq GRCh38/hg38
XM_011532084.2 chr4:g.152326215G>C c.1435C>G p.R479G RefSeq GRCh38/hg38
XM_011532084.3 chr4:g.152326215G>C c.1435C>G p.R479G RefSeq GRCh38/hg38

Filtering

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