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Gene | FBXW7 |
Variant | S398F |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | FBXW7 S398F lies within WD repeat 1 of the Fbxw7 protein (UniProt.org). S398F has been identified in sequencing studies (PMID: 29996881, PMID: 37116140), 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 S398F |
Transcript | NM_033632.3 |
gDNA | chr4:g.152329715G>A |
cDNA | c.1193C>T |
Protein | p.S398F |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_018315.5 | chr4:g.152326217G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
XM_011532084 | chr4:g.152329715G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
XM_024454124.1 | chr4:g.152329715G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
XM_024454121.1 | chr4:g.152329715G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
XM_011532084.3 | chr4:g.152329715G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
NM_001013415.1 | chr4:g.152326103_152326104delAGinsTT | c.1192_1193delAGinsTT | p.S398F | RefSeq | GRCh38/hg38 |
XM_024454123.2 | chr4:g.152329715G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
XM_047415899.1 | chr4:g.152329715G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
XM_047415897.1 | chr4:g.152329715G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
NM_001013415 | chr4:g.152326103_152326104delCTinsAA | c.1192_1193delAGinsTT | p.S398F | RefSeq | GRCh38/hg38 |
XM_011532087.3 | chr4:g.152328348_152328349delCAinsTT | c.1193_1194delCAinsTT | p.S398F | RefSeq | GRCh38/hg38 |
XM_047415898.1 | chr4:g.152329715G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
NM_018315 | chr4:g.152326217G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
XM_024454122.1 | chr4:g.152329715G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
XM_011532086.3 | chr4:g.152328348_152328349delCAinsTT | c.1193_1194delCAinsTT | p.S398F | RefSeq | GRCh38/hg38 |
XM_011532086.2 | chr4:g.152328348_152328349delCAinsTT | c.1193_1194delCAinsTT | p.S398F | RefSeq | GRCh38/hg38 |
XM_047415902.1 | chr4:g.152328348_152328349delCAinsTT | c.1193_1194delCAinsTT | p.S398F | RefSeq | GRCh38/hg38 |
NM_018315.4 | chr4:g.152326217G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
NM_001349798.2 | chr4:g.152329715G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
XM_011532087 | chr4:g.152328348_152328349delTGinsAA | c.1193_1194delCAinsTT | p.S398F | RefSeq | GRCh38/hg38 |
XM_047415901.1 | chr4:g.152329715G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
NM_033632.3 | chr4:g.152329715G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
XM_011532083 | chr4:g.152329715G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
XM_011532085.2 | chr4:g.152329715G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
XM_011532087.2 | chr4:g.152328348_152328349delCAinsTT | c.1193_1194delCAinsTT | p.S398F | RefSeq | GRCh38/hg38 |
NM_001013415.2 | chr4:g.152326103_152326104delAGinsTT | c.1192_1193delAGinsTT | p.S398F | RefSeq | GRCh38/hg38 |
XM_011532085.3 | chr4:g.152329715G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
NM_033632.3 | chr4:g.152329715G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
XM_011532085 | chr4:g.152329715G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
NM_001349798.1 | chr4:g.152329715G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
XM_011532086 | chr4:g.152328348_152328349delTGinsAA | c.1193_1194delCAinsTT | p.S398F | RefSeq | GRCh38/hg38 |
XM_024454123.1 | chr4:g.152329715G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
XM_047415900.1 | chr4:g.152329715G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
XM_011532084.2 | chr4:g.152329715G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
XM_024454125.1 | chr4:g.152328348_152328349delCAinsTT | c.1193_1194delCAinsTT | p.S398F | RefSeq | GRCh38/hg38 |
XM_017008362 | chr4:g.152329715G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
NM_033632 | chr4:g.152329715G>A | c.1193C>T | p.S398F | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
FBXW7 S398F | unknown |