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Gene FBXW7
Variant G499Vfs*25
Impact List frameshift
Protein Effect loss of function - predicted
Gene Variant Descriptions FBXW7 G499Vfs*25 indicates a shift in the reading frame starting at amino acid 499 and terminating 25 residues downstream causing a premature truncation of the 707 amino acid Fbxw7 protein (UniProt.org). Due to the loss of multiple WD domains (UniProt.org), G499Vfs*25 is predicted to lead to a loss of Fbxw7 protein function.
Associated Drug Resistance
Category Variants Paths

FBXW7 mutant FBXW7 inact mut FBXW7 G499Vfs*25

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Transcript NM_033632.3
gDNA chr4:g.152326156delC
cDNA c.1496delG
Protein p.G499Vfs*25
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_011532084.3 chr4:g.152326156delC c.1496delG p.G499Vfs*25 RefSeq GRCh38/hg38
XM_011532085.3 chr4:g.152326156delC c.1496delG p.G499Vfs*25 RefSeq GRCh38/hg38
XM_011532088 chr4:g.(152322932_152323009) c.(1495_1572) p.G499Vfs*25 RefSeq GRCh38/hg38
NM_018315 chr4:g.(152324227_152324304) c.(1495_1572) p.G499Vfs*25 RefSeq GRCh38/hg38
XM_024454126.1 chr4:g.(152322932_152323009) c.(1495_1572) p.G499Vfs*25 RefSeq GRCh38/hg38
NM_018315.4 chr4:g.(152324227_152324304) c.(1495_1572) p.G499Vfs*25 RefSeq GRCh38/hg38
XM_024454121.1 chr4:g.152326156delC c.1496delG p.G499Vfs*25 RefSeq GRCh38/hg38
NM_033632.3 chr4:g.152326156delC c.1496delG p.G499Vfs*25 RefSeq GRCh38/hg38
XM_047415898.1 chr4:g.152326156delC c.1496delG p.G499Vfs*25 RefSeq GRCh38/hg38
NM_033632.3 chr4:g.152326156delC c.1496delG p.G499Vfs*25 RefSeq GRCh38/hg38
XM_017008362 chr4:g.152326156delC c.1496delG p.G499Vfs*25 RefSeq GRCh38/hg38
XM_024454122.1 chr4:g.152326156delC c.1496delG p.G499Vfs*25 RefSeq GRCh38/hg38
NM_018315.5 chr4:g.(152324227_152324304) c.(1495_1572) p.G499Vfs*25 RefSeq GRCh38/hg38
XM_011532085.2 chr4:g.152326156delC c.1496delG p.G499Vfs*25 RefSeq GRCh38/hg38
NM_033632 chr4:g.152326156delC c.1496delG p.G499Vfs*25 RefSeq GRCh38/hg38
NM_001349798.1 chr4:g.152326156delC c.1496delG p.G499Vfs*25 RefSeq GRCh38/hg38
XM_047415897.1 chr4:g.152326156delC c.1496delG p.G499Vfs*25 RefSeq GRCh38/hg38
XM_047415899.1 chr4:g.152326156delC c.1496delG p.G499Vfs*25 RefSeq GRCh38/hg38
XM_024454124.1 chr4:g.152326156delC c.1496delG p.G499Vfs*25 RefSeq GRCh38/hg38
XM_024454123.1 chr4:g.152326156delC c.1496delG p.G499Vfs*25 RefSeq GRCh38/hg38
XM_011532084.2 chr4:g.152326156delC c.1496delG p.G499Vfs*25 RefSeq GRCh38/hg38
XM_011532088.2 chr4:g.(152322932_152323009) c.(1495_1572) p.G499Vfs*25 RefSeq GRCh38/hg38
XM_011532084 chr4:g.152326156delC c.1496delG p.G499Vfs*25 RefSeq GRCh38/hg38
XM_047415901.1 chr4:g.152326156delC c.1496delG p.G499Vfs*25 RefSeq GRCh38/hg38
XM_024454123.2 chr4:g.152326156delC c.1496delG p.G499Vfs*25 RefSeq GRCh38/hg38
XM_011532085 chr4:g.152326156delC c.1496delG p.G499Vfs*25 RefSeq GRCh38/hg38
XM_047415900.1 chr4:g.152326156delC c.1496delG p.G499Vfs*25 RefSeq GRCh38/hg38
NM_001349798.2 chr4:g.152326156delC c.1496delG p.G499Vfs*25 RefSeq GRCh38/hg38
XM_024454126.2 chr4:g.(152322932_152323009) c.(1495_1572) p.G499Vfs*25 RefSeq GRCh38/hg38
XM_011532083 chr4:g.152326156delC c.1496delG p.G499Vfs*25 RefSeq GRCh38/hg38

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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 inact mut Advanced Solid Tumor resistant Docetaxel Preclinical Actionable In a preclinical study, human cancer cell lines harboring FBXW7 inactivating mutations were resistant to docetaxel in culture (PMID: 23274910). 23274910
FBXW7 inact mut breast cancer sensitive Sirolimus Preclinical - Cell line xenograft Actionable In a preclinical study, breast cancer cells harboring a FBXW7 mutation demonstrated sensitivity to Rapamune (sirolimus) in culture and in cell line xenograft models (PMID: 18787170). 18787170
FBXW7 inact mut hematologic cancer sensitive REC-2282 Preclinical Actionable In a preclinical study, REC-2282 (AR-42) inhibited human hematologic cancer cell lines harboring FBXW7 inactivating mutations in culture (PMID: 23274910). 23274910
FBXW7 inact mut hematologic cancer sensitive Belinostat Preclinical Actionable In a preclinical study, Beleodaq (belinostat) inhibited human hematologic cancer cell lines harboring FBXW7 inactivating mutations in culture (PMID: 23274910). 23274910
FBXW7 inact mut hematologic cancer sensitive Entinostat Preclinical Actionable In a preclinical study, entinostat (MS-275) inhibited cancer cells from advanced solid tumors and hematological cells harboring FBXW7 inactivating mutations in culture (PMID: 23274910). 23274910
FBXW7 inact mut Advanced Solid Tumor sensitive Entinostat Preclinical Actionable In a preclinical study, entinostat (MS-275) inhibited cancer cells from advanced solid tumors and hematological cells harboring FBXW7 inactivating mutations in culture (PMID: 23274910). 23274910
FBXW7 inact mut Advanced Solid Tumor sensitive REC-2282 Preclinical Actionable In a preclinical study, REC-2282 (AR-42) inhibited human cancer cell lines harboring FBXW7 inactivating mutations in culture (PMID: 23274910). 23274910
FBXW7 inact mut Advanced Solid Tumor sensitive Belinostat Preclinical Actionable In a preclinical study, Beleodaq (belinostat) inhibited human cancer cell lines harboring FBXW7 inactivating mutations in culture (PMID: 23274910). 23274910
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