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Gene | FBXW7 |
Variant | R465P |
Impact List | missense |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | FBXW7 R465P lies within the WD repeat domain of the Fbxw7 protein (UniProt.org). R465P has not been characterized however, other R465 hotspots inactivate Fbxw7, and therefore, R465P is predicted to lead to a loss of function (PMID: 17646409, PMID: 17909001, PMID: 19340001). |
Associated Drug Resistance | |
Category Variants Paths |
FBXW7 mutant FBXW7 inact mut FBXW7 R465P |
Transcript | NM_033632.3 |
gDNA | chr4:g.152328232C>G |
cDNA | c.1394G>C |
Protein | p.R465P |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_011532084.3 | chr4:g.152328232C>G | c.1394G>C | p.R465P | RefSeq | GRCh38/hg38 |
XM_024454123.1 | chr4:g.152328232C>G | c.1394G>C | p.R465P | RefSeq | GRCh38/hg38 |
NM_001349798.2 | chr4:g.152328232C>G | c.1394G>C | p.R465P | RefSeq | GRCh38/hg38 |
XM_011532084.2 | chr4:g.152328232C>G | c.1394G>C | p.R465P | RefSeq | GRCh38/hg38 |
XM_024454123.2 | chr4:g.152328232C>G | c.1394G>C | p.R465P | RefSeq | GRCh38/hg38 |
XM_047415900.1 | chr4:g.152328232C>G | c.1394G>C | p.R465P | RefSeq | GRCh38/hg38 |
XM_047415901.1 | chr4:g.152328232C>G | c.1394G>C | p.R465P | RefSeq | GRCh38/hg38 |
XM_047415898.1 | chr4:g.152328232C>G | c.1394G>C | p.R465P | RefSeq | GRCh38/hg38 |
XM_024454121.1 | chr4:g.152328232C>G | c.1394G>C | p.R465P | RefSeq | GRCh38/hg38 |
NM_001349798.1 | chr4:g.152328232C>G | c.1394G>C | p.R465P | RefSeq | GRCh38/hg38 |
XM_011532084 | chr4:g.152328232C>G | c.1394G>C | p.R465P | RefSeq | GRCh38/hg38 |
XM_011532085.3 | chr4:g.152328232C>G | c.1394G>C | p.R465P | RefSeq | GRCh38/hg38 |
NM_033632.3 | chr4:g.152328232C>G | c.1394G>C | p.R465P | RefSeq | GRCh38/hg38 |
XM_011532083 | chr4:g.152328232C>G | c.1394G>C | p.R465P | RefSeq | GRCh38/hg38 |
XM_011532085.2 | chr4:g.152328232C>G | c.1394G>C | p.R465P | RefSeq | GRCh38/hg38 |
XM_017008362 | chr4:g.152328232C>G | c.1394G>C | p.R465P | RefSeq | GRCh38/hg38 |
XM_047415897.1 | chr4:g.152328232C>G | c.1394G>C | p.R465P | RefSeq | GRCh38/hg38 |
NM_033632 | chr4:g.152328232C>G | c.1394G>C | p.R465P | RefSeq | GRCh38/hg38 |
XM_011532085 | chr4:g.152328232C>G | c.1394G>C | p.R465P | RefSeq | GRCh38/hg38 |
XM_047415899.1 | chr4:g.152328232C>G | c.1394G>C | p.R465P | RefSeq | GRCh38/hg38 |
XM_024454124.1 | chr4:g.152328232C>G | c.1394G>C | p.R465P | RefSeq | GRCh38/hg38 |
XM_024454122.1 | chr4:g.152328232C>G | c.1394G>C | p.R465P | RefSeq | GRCh38/hg38 |
NM_033632.3 | chr4:g.152328232C>G | c.1394G>C | p.R465P | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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