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Gene | KIT |
Variant | W557_K558delinsF |
Impact List | indel |
Protein Effect | gain of function - predicted |
Gene Variant Descriptions | KIT W557_K558delinsF results in a deletion of two amino acids in the juxtamembrane domain (exon 11) of the Kit protein from amino acids 557 to 558, combined with the insertion of a phenylalanine (F) at the same site (PMID: 16226710). KIT W557_K558delinsF has not been characterized, however similar Kit exon 11 deletions are activating (PMID: 9438854, PMID: 15365079), 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 exon 11 del KIT W557_K558delinsF KIT mutant KIT exon11 KIT exon 11 del KIT W557_K558delinsF |
Transcript | NM_000222.3 |
gDNA | chr4:g.54727437_54727442delinsTTT |
cDNA | c.1669_1674delinsTTT |
Protein | p.W557_K558delinsF |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_001385285.1 | chr4:g.54727437_54727442delinsTTT | c.1669_1674delinsTTT | p.W557_K558delinsF | RefSeq | GRCh38/hg38 |
NM_000222 | chr4:g.54727437_54727442delinsTTT | c.1669_1674delinsTTT | p.W557_K558delinsF | RefSeq | GRCh38/hg38 |
XM_017008178 | chr4:g.54727437_54727442delinsTTT | c.1669_1674delinsTTT | p.W557_K558delinsF | RefSeq | GRCh38/hg38 |
XM_017008178.1 | chr4:g.54727437_54727442delinsTTT | c.1669_1674delinsTTT | p.W557_K558delinsF | RefSeq | GRCh38/hg38 |
NM_000222.3 | chr4:g.54727437_54727442delinsTTT | c.1669_1674delinsTTT | p.W557_K558delinsF | RefSeq | GRCh38/hg38 |
NM_000222.2 | chr4:g.54727437_54727442delinsTTT | c.1669_1674delinsTTT | p.W557_K558delinsF | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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