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Gene FBXW7
Variant S582P
Impact List missense
Protein Effect unknown
Gene Variant Descriptions FBXW7 S582P lies within WD repeat 6 of the Fbxw7 protein (UniProt.org). S582P has been identified in sequencing studies (PMID: 29316426), but has not been biochemically characterized and therefore, its effect on Fbxw7 protein function is unknown (PubMed, Oct 2024).
Associated Drug Resistance
Category Variants Paths

FBXW7 mutant FBXW7 S582P

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Transcript NM_033632.3
gDNA chr4:g.152324295A>G
cDNA c.1744T>C
Protein p.S582P
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001349798.1 chr4:g.152324295A>G c.1744T>C p.S582P RefSeq GRCh38/hg38
XM_047415899.1 chr4:g.152324295A>G c.1744T>C p.S582P RefSeq GRCh38/hg38
NM_001349798.2 chr4:g.152324295A>G c.1744T>C p.S582P RefSeq GRCh38/hg38
XM_024454121.1 chr4:g.152324295A>G c.1744T>C p.S582P RefSeq GRCh38/hg38
XM_047415898.1 chr4:g.152324295A>G c.1744T>C p.S582P RefSeq GRCh38/hg38
XM_011532085.2 chr4:g.152324295A>G c.1744T>C p.S582P RefSeq GRCh38/hg38
XM_024454123.1 chr4:g.152324295A>G c.1744T>C p.S582P RefSeq GRCh38/hg38
XM_024454122.1 chr4:g.152324295A>G c.1744T>C p.S582P RefSeq GRCh38/hg38
XM_024454123.2 chr4:g.152324295A>G c.1744T>C p.S582P RefSeq GRCh38/hg38
XM_047415901.1 chr4:g.152324295A>G c.1744T>C p.S582P RefSeq GRCh38/hg38
NM_033632.3 chr4:g.152324295A>G c.1744T>C p.S582P RefSeq GRCh38/hg38
NM_033632.3 chr4:g.152324295A>G c.1744T>C p.S582P RefSeq GRCh38/hg38
XM_047415897.1 chr4:g.152324295A>G c.1744T>C p.S582P RefSeq GRCh38/hg38
XM_047415900.1 chr4:g.152324295A>G c.1744T>C p.S582P RefSeq GRCh38/hg38
XM_024454124.1 chr4:g.152324295A>G c.1744T>C p.S582P RefSeq GRCh38/hg38
XM_011532085.3 chr4:g.152324295A>G c.1744T>C p.S582P RefSeq GRCh38/hg38
XM_011532084.2 chr4:g.152324295A>G c.1744T>C p.S582P RefSeq GRCh38/hg38
XM_011532084.3 chr4:g.152324295A>G c.1744T>C p.S582P RefSeq GRCh38/hg38

Filtering

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  • Separate multiple filter terms with a space. Any order may be used (i. e. a b c and c b a are equivalent )
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  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References
FBXW7 mutant Her2-receptor negative breast cancer predicted - sensitive LY3039478 Case Reports/Case Series Actionable In a Phase I trial, LY3039478 treatment resulted in partial response lasted 9.5 months in a patient with hormone receptor-positive, Erbb2 (Her2)-negative breast cancer harboring FBXW7 mutation (PMID: 30060061; NCT01695005). 30060061