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Gene | FBXW7 |
Variant | S546P |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | FBXW7 S546P lies within WD repeat 5 of the Fbxw7 protein (UniProt.org). S546P 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 S546P |
Transcript | NM_033632.3 |
gDNA | chr4:g.152326014A>G |
cDNA | c.1636T>C |
Protein | p.S546P |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_024454121.1 | chr4:g.152326014A>G | c.1636T>C | p.S546P | RefSeq | GRCh38/hg38 |
XM_011532084.3 | chr4:g.152326014A>G | c.1636T>C | p.S546P | RefSeq | GRCh38/hg38 |
XM_024454123.1 | chr4:g.152326014A>G | c.1636T>C | p.S546P | RefSeq | GRCh38/hg38 |
XM_011532085.3 | chr4:g.152326014A>G | c.1636T>C | p.S546P | RefSeq | GRCh38/hg38 |
XM_047415899.1 | chr4:g.152326014A>G | c.1636T>C | p.S546P | RefSeq | GRCh38/hg38 |
XM_047415901.1 | chr4:g.152326014A>G | c.1636T>C | p.S546P | RefSeq | GRCh38/hg38 |
XM_047415898.1 | chr4:g.152326014A>G | c.1636T>C | p.S546P | RefSeq | GRCh38/hg38 |
NM_001349798.2 | chr4:g.152326014A>G | c.1636T>C | p.S546P | RefSeq | GRCh38/hg38 |
XM_024454123.2 | chr4:g.152326014A>G | c.1636T>C | p.S546P | RefSeq | GRCh38/hg38 |
NM_001349798.1 | chr4:g.152326014A>G | c.1636T>C | p.S546P | RefSeq | GRCh38/hg38 |
NM_033632.3 | chr4:g.152326014A>G | c.1636T>C | p.S546P | RefSeq | GRCh38/hg38 |
XM_011532084.2 | chr4:g.152326014A>G | c.1636T>C | p.S546P | RefSeq | GRCh38/hg38 |
XM_024454122.1 | chr4:g.152326014A>G | c.1636T>C | p.S546P | RefSeq | GRCh38/hg38 |
XM_011532085.2 | chr4:g.152326014A>G | c.1636T>C | p.S546P | RefSeq | GRCh38/hg38 |
NM_033632.3 | chr4:g.152326014A>G | c.1636T>C | p.S546P | RefSeq | GRCh38/hg38 |
XM_024454124.1 | chr4:g.152326014A>G | c.1636T>C | p.S546P | RefSeq | GRCh38/hg38 |
XM_047415897.1 | chr4:g.152326014A>G | c.1636T>C | p.S546P | RefSeq | GRCh38/hg38 |
XM_047415900.1 | chr4:g.152326014A>G | c.1636T>C | p.S546P | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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