Missing content? – Request curation!
Request curation for specific Genes, Variants, or PubMed publications.
Have questions, comments, or suggestions? - Let us know!
Email us at : ckbsupport@genomenon.com
Gene | KIT |
Variant | F522C |
Impact List | missense |
Protein Effect | gain of function - predicted |
Gene Variant Descriptions | KIT F522C lies within the transmembrane domain of the Kit protein (PMID: 15070706). F522C results in ligand independent autophosphorylation of Kit in cell culture (PMID: 15070706), and therefore, is predicted to lead to a gain of Kit protein function. |
Associated Drug Resistance | |
Category Variants Paths |
KIT mutant KIT act mut KIT F522C |
Transcript | NM_000222.3 |
gDNA | chr4:g.54727242T>G |
cDNA | c.1565T>G |
Protein | p.F522C |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_017008178.1 | chr4:g.54727242T>G | c.1565T>G | p.F522C | RefSeq | GRCh38/hg38 |
NM_000222.2 | chr4:g.54727242T>G | c.1565T>G | p.F522C | RefSeq | GRCh38/hg38 |
NM_001385285.1 | chr4:g.54727242T>G | c.1565T>G | p.F522C | RefSeq | GRCh38/hg38 |
XM_017008178 | chr4:g.54727242T>G | c.1565T>G | p.F522C | RefSeq | GRCh38/hg38 |
NM_000222.3 | chr4:g.54727242T>G | c.1565T>G | p.F522C | RefSeq | GRCh38/hg38 |
NM_000222 | chr4:g.54727242T>G | c.1565T>G | p.F522C | RefSeq | GRCh38/hg38 |
Molecular Profile | Protein Effect | Treatment Approaches |
---|---|---|
KIT F522C | gain of function - predicted | KIT Inhibitor |