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Gene | KIT |
Variant | E562K |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | KIT E562K lies within the cytoplasmic domain of the Kit protein (UniProt.org). E562K has been identified in sequencing studies (PMID: 20861712), but has not been biochemically characterized and therefore, its effect on Kit protein function is unknown (PubMed, Nov 2024). |
Associated Drug Resistance | |
Category Variants Paths |
KIT mutant KIT exon11 KIT E562K |
Transcript | NM_000222.3 |
gDNA | chr4:g.54727452G>A |
cDNA | c.1684G>A |
Protein | p.E562K |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_000222.3 | chr4:g.54727452G>A | c.1684G>A | p.E562K | RefSeq | GRCh38/hg38 |
NM_001385285.1 | chr4:g.54727452G>A | c.1684G>A | p.E562K | RefSeq | GRCh38/hg38 |
XM_005265740 | chr4:g.54727449G>A | c.1684G>A | p.E562K | RefSeq | GRCh38/hg38 |
XM_005265740.1 | chr4:g.54727449G>A | c.1684G>A | p.E562K | RefSeq | GRCh38/hg38 |
NM_000222 | chr4:g.54727452G>A | c.1684G>A | p.E562K | RefSeq | GRCh38/hg38 |
NM_001385290.1 | chr4:g.54727449G>A | c.1684G>A | p.E562K | RefSeq | GRCh38/hg38 |
XM_017008178 | chr4:g.54727452G>A | c.1684G>A | p.E562K | RefSeq | GRCh38/hg38 |
NM_001385284.1 | chr4:g.54727449G>A | c.1684G>A | p.E562K | RefSeq | GRCh38/hg38 |
XM_005265741 | chr4:g.54727449G>A | c.1684G>A | p.E562K | RefSeq | GRCh38/hg38 |
NM_000222.2 | chr4:g.54727452G>A | c.1684G>A | p.E562K | RefSeq | GRCh38/hg38 |
XM_017008178.1 | chr4:g.54727452G>A | c.1684G>A | p.E562K | RefSeq | GRCh38/hg38 |
XM_005265741.1 | chr4:g.54727449G>A | c.1684G>A | p.E562K | RefSeq | GRCh38/hg38 |
Clinical Trial | Phase | Therapies | Title | Recruitment Status | Covered Countries | Other Countries |
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