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 | W557Lfs*5 |
Impact List | frameshift |
Protein Effect | loss of function - predicted |
Gene Variant Descriptions | KIT W557Lfs*5 indicates a shift in the reading frame starting at amino acid 557 and terminating 5 residues downstream causing a premature truncation of the 976 amino acid Kit protein (UniProt.org). Due to the loss of the protein kinase domain (UniProt.org), W557Lfs*5 is predicted to lead to a loss of Kit protein function. |
Associated Drug Resistance | |
Category Variants Paths |
KIT mutant KIT exon11 KIT W557Lfs*5 |
Transcript | NM_000222.3 |
gDNA | chr4:g.54727437dupT |
cDNA | c.1669dupT |
Protein | p.W557Lfs*5 |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_017008178 | chr4:g.54727436_54727437insC | c.1668_1669insC | p.W557Lfs*5 | RefSeq | GRCh38/hg38 |
NM_000222.3 | chr4:g.54727437dupT | c.1669dupT | p.W557Lfs*5 | RefSeq | GRCh38/hg38 |
NM_001385285.1 | chr4:g.54727437dupT | c.1669dupT | p.W557Lfs*5 | RefSeq | GRCh38/hg38 |
NM_000222.2 | chr4:g.54727437dupT | c.1669dupT | p.W557Lfs*5 | RefSeq | GRCh38/hg38 |
NM_000222 | chr4:g.54727436_54727437insC | c.1668_1669insC | p.W557Lfs*5 | RefSeq | GRCh38/hg38 |
XM_017008178.1 | chr4:g.54727437dupT | c.1669dupT | p.W557Lfs*5 | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
---|