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Gene | FBXW7 |
Variant | L443H |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | FBXW7 L443H lies within WD repeat 2 of the Fbxw7 protein (UniProt.org). L443H results in increased migration and invasion, but has no effect on cell proliferation and variable effect on colony formation in culture (PMID: 31161818), and therefore, its effect on Fbxw7 protein is unknown. |
Associated Drug Resistance | |
Category Variants Paths |
FBXW7 mutant FBXW7 L443H |
Transcript | NM_033632.3 |
gDNA | chr4:g.152328298A>T |
cDNA | c.1328T>A |
Protein | p.L443H |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_024454123.1 | chr4:g.152328298A>T | c.1328T>A | p.L443H | RefSeq | GRCh38/hg38 |
XM_011532085.3 | chr4:g.152328298A>T | c.1328T>A | p.L443H | RefSeq | GRCh38/hg38 |
XM_017008362 | chr4:g.152328298A>T | c.1328T>A | p.L443H | RefSeq | GRCh38/hg38 |
XM_047415899.1 | chr4:g.152328298A>T | c.1328T>A | p.L443H | RefSeq | GRCh38/hg38 |
XM_011532085 | chr4:g.152328298A>T | c.1328T>A | p.L443H | RefSeq | GRCh38/hg38 |
NM_033632.3 | chr4:g.152328298A>T | c.1328T>A | p.L443H | RefSeq | GRCh38/hg38 |
XM_024454121.1 | chr4:g.152328298A>T | c.1328T>A | p.L443H | RefSeq | GRCh38/hg38 |
XM_047415900.1 | chr4:g.152328298A>T | c.1328T>A | p.L443H | RefSeq | GRCh38/hg38 |
XM_011532084.3 | chr4:g.152328298A>T | c.1328T>A | p.L443H | RefSeq | GRCh38/hg38 |
XM_047415898.1 | chr4:g.152328298A>T | c.1328T>A | p.L443H | RefSeq | GRCh38/hg38 |
XM_047415897.1 | chr4:g.152328298A>T | c.1328T>A | p.L443H | RefSeq | GRCh38/hg38 |
XM_024454122.1 | chr4:g.152328298A>T | c.1328T>A | p.L443H | RefSeq | GRCh38/hg38 |
XM_047415901.1 | chr4:g.152328298A>T | c.1328T>A | p.L443H | RefSeq | GRCh38/hg38 |
NM_033632.3 | chr4:g.152328298A>T | c.1328T>A | p.L443H | RefSeq | GRCh38/hg38 |
XM_024454123.2 | chr4:g.152328298A>T | c.1328T>A | p.L443H | RefSeq | GRCh38/hg38 |
NM_001349798.2 | chr4:g.152328298A>T | c.1328T>A | p.L443H | RefSeq | GRCh38/hg38 |
NM_001349798.1 | chr4:g.152328298A>T | c.1328T>A | p.L443H | RefSeq | GRCh38/hg38 |
XM_011532085.2 | chr4:g.152328298A>T | c.1328T>A | p.L443H | RefSeq | GRCh38/hg38 |
XM_011532083 | chr4:g.152328298A>T | c.1328T>A | p.L443H | RefSeq | GRCh38/hg38 |
XM_011532084.2 | chr4:g.152328298A>T | c.1328T>A | p.L443H | RefSeq | GRCh38/hg38 |
XM_024454124.1 | chr4:g.152328298A>T | c.1328T>A | p.L443H | RefSeq | GRCh38/hg38 |
XM_011532084 | chr4:g.152328298A>T | c.1328T>A | p.L443H | RefSeq | GRCh38/hg38 |
NM_033632 | chr4:g.152328298A>T | c.1328T>A | p.L443H | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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