Gene Variant Detail

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Gene KIT
Variant K558_Y570delinsNP
Impact List indel
Protein Effect gain of function - predicted
Gene Variant Descriptions KIT K558_Y570delinsNP results in a deletion of thirteen amino acids in the juxtamembrane domain (exon 11) of the Kit protein from amino acids 558 to 570, combined with the insertion of an asparagine (N) and a proline (P) at the same site (PMID: 16226710). K558_Y570delinsNP 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 K558_Y570delinsNP

KIT mutant KIT exon11 KIT exon 11 del KIT K558_Y570delinsNP

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Transcript NM_000222.3
gDNA chr4:g.54727440_54727478delinsAACCCT
cDNA c.1672_1710delinsAACCCT
Protein p.K558_Y570delinsNP
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_000222.2 chr4:g.54727440_54727478delinsAACCCT c.1672_1710delinsAACCCT p.K558_Y570delinsNP RefSeq GRCh38/hg38
NM_000222 chr4:g.54727440_54727478delinsAACCCT c.1672_1710delinsAACCCT p.K558_Y570delinsNP RefSeq GRCh38/hg38
NM_001385285.1 chr4:g.54727440_54727478delinsAACCCT c.1672_1710delinsAACCCT p.K558_Y570delinsNP RefSeq GRCh38/hg38
XM_017008178 chr4:g.54727440_54727478delinsAACCCT c.1672_1710delinsAACCCT p.K558_Y570delinsNP RefSeq GRCh38/hg38
XM_017008178.1 chr4:g.54727440_54727478delinsAACCCT c.1672_1710delinsAACCCT p.K558_Y570delinsNP RefSeq GRCh38/hg38
NM_000222.3 chr4:g.54727440_54727478delinsAACCCT c.1672_1710delinsAACCCT p.K558_Y570delinsNP RefSeq GRCh38/hg38

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  • Use simple literal full or partial string matches
  • Separate multiple filter terms with a space. Any order may be used (i. e. a b c and c b a are equivalent )
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  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

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Clinical Trial Phase Therapies Title Recruitment Status Covered Countries Other Countries