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Gene | KIT |
Variant | T22A |
Impact List | missense |
Protein Effect | unknown |
Gene Variant Descriptions | KIT T22A lies within the signal peptide region of the Kit protein (UniProt.org). T22A has been identified in sequencing studies (PMID: 21720365), 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 T22A |
Transcript | NM_000222.3 |
gDNA | chr4:g.54658078A>G |
cDNA | c.64A>G |
Protein | p.T22A |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
XM_005265740.1 | chr4:g.54658078A>G | c.64A>G | p.T22A | RefSeq | GRCh38/hg38 |
NM_000222.3 | chr4:g.54658078A>G | c.64A>G | p.T22A | RefSeq | GRCh38/hg38 |
XM_005265742 | chr4:g.54658078A>G | c.64A>G | p.T22A | RefSeq | GRCh38/hg38 |
NM_001093772.1 | chr4:g.54658078A>G | c.64A>G | p.T22A | RefSeq | GRCh38/hg38 |
XM_017008180 | chr4:g.54658078A>G | c.64A>G | p.T22A | RefSeq | GRCh38/hg38 |
XM_005265741.1 | chr4:g.54658078A>G | c.64A>G | p.T22A | RefSeq | GRCh38/hg38 |
NM_001385288.1 | chr4:g.54658078A>G | c.64A>G | p.T22A | RefSeq | GRCh38/hg38 |
XM_005265741 | chr4:g.54658078A>G | c.64A>G | p.T22A | RefSeq | GRCh38/hg38 |
XM_005265742.3 | chr4:g.54658078A>G | c.64A>G | p.T22A | RefSeq | GRCh38/hg38 |
XM_005265740 | chr4:g.54658078A>G | c.64A>G | p.T22A | RefSeq | GRCh38/hg38 |
NM_000222.2 | chr4:g.54658078A>G | c.64A>G | p.T22A | RefSeq | GRCh38/hg38 |
NM_001385285.1 | chr4:g.54658078A>G | c.64A>G | p.T22A | RefSeq | GRCh38/hg38 |
XM_017008179 | chr4:g.54658078A>G | c.64A>G | p.T22A | RefSeq | GRCh38/hg38 |
NM_001385286.1 | chr4:g.54658078A>G | c.64A>G | p.T22A | RefSeq | GRCh38/hg38 |
XM_017008178.1 | chr4:g.54658078A>G | c.64A>G | p.T22A | RefSeq | GRCh38/hg38 |
XM_017008180.1 | chr4:g.54658078A>G | c.64A>G | p.T22A | RefSeq | GRCh38/hg38 |
NM_001093772.2 | chr4:g.54658078A>G | c.64A>G | p.T22A | RefSeq | GRCh38/hg38 |
NM_001093772 | chr4:g.54658078A>G | c.64A>G | p.T22A | RefSeq | GRCh38/hg38 |
NM_001385292.1 | chr4:g.54658078A>G | c.64A>G | p.T22A | RefSeq | GRCh38/hg38 |
XM_017008178 | chr4:g.54658078A>G | c.64A>G | p.T22A | RefSeq | GRCh38/hg38 |
XM_017008179.1 | chr4:g.54658078A>G | c.64A>G | p.T22A | RefSeq | GRCh38/hg38 |
NM_000222 | chr4:g.54658078A>G | c.64A>G | p.T22A | RefSeq | GRCh38/hg38 |
NM_001385284.1 | chr4:g.54658078A>G | c.64A>G | p.T22A | RefSeq | GRCh38/hg38 |
NM_001385290.1 | chr4:g.54658078A>G | c.64A>G | p.T22A | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
---|---|---|---|---|---|---|---|
KIT mutant | melanoma | sensitive | Nilotinib | Phase II | Actionable | In a Phase II trial, Tasigna (nilotinib) treatment in patients with melanoma harboring KIT mutations resulted in an overall response rate of 26.2% (11/42), which included 11 patients with a partial response, a median duration of response of 7.1 months, and an overall survival of 18 months (PMID: 28327988; NCT01028222). | 28327988 |
KIT mutant | melanoma | sensitive | Nilotinib | Phase II | Actionable | In a Phase II trial, Tasigna (nilotinib) treatment resulted in complete response in 4% (1/25), durable partial response in 16% (4/25), and stable disease in 56% (14/25) of melanoma patients harboring KIT mutations (PMID: 28843487; NCT01168050). | 28843487 |
KIT mutant | gastrointestinal stromal tumor | predicted - sensitive | Ripretinib | Phase I | Actionable | In a Phase I trial, Qinlock (ripretinib) demonstrated preliminary safety and efficacy in patients with advanced solid tumors, including KIT-mutant gastrointestinal stromal tumor (GIST), with 1 patient harboring KIT exon 11 and 17 mutations demonstrating a partial response, and 7/7 KIT-mutant GIST patients demonstrating a partial metabolic response (EORTC-NCI-AACR 2016, Abs 7LBA). | detail... |
KIT mutant | gastrointestinal stromal tumor | predicted - sensitive | Ripretinib | Phase I | Actionable | In a Phase I trial, Qinlock (ripretinib) was well tolerated, resulted in an objective response in 11.3% (16/142, 16 partial responses) and stable disease in 61.3% (87/142) of patients with advanced gastrointestinal stromal tumor harboring KIT (exon 11, n=103; exon 9, n=26; other, n=6) or PDGFRA mutations (n=7), with a median progression-free survival of 5.6 months (PMID: 32804590; NCT02571036). | 32804590 |
KIT mutant | gastrointestinal stromal tumor | not applicable | N/A | Clinical Study | Diagnostic | KIT mutations are used in the diagnosis of gastrointestinal stromal tumors (PMID: 25193432, PMID: 26276366, PMID: 25729899). | 25193432 26276366 25729899 |
KIT mutant | gastrointestinal stromal tumor | predicted - sensitive | Avapritinib | Phase I | Actionable | In a Phase I (NAVIGATOR) trial, Ayvakit (avapritinib) treatment resulted in an objective response rate of 13% (7/52, 7 partial responses) and a disease control rate of 63% (33/52) in patients with KIT-mutant gastrointestinal stromal tumor (The CTOS 2018 Annual Meeting, Nov 14-17, Rome Italy, Paper 012 3027631; NCT02508532). | detail... |
KIT mutant | melanoma | predicted - sensitive | Ripretinib | Phase I | Actionable | In a Phase I trial, Qinlock (ripretinib) treatment demonstrated manageable safety and preliminary efficacy in patients with KIT-mutated melanoma, and led to an objective response rate of 23% (6/26, 1 complete and 5 partial responses), a median progression-free survival of 7.3 months, and a median duration of response of 9.1 months (PMID: 35753087; NCT02571036). | 35753087 |
KIT mutant | gastrointestinal stromal tumor | sensitive | Imatinib + Infigratinib | Preclinical - Pdx | Actionable | In a preclinical study, Truseltiq (infigratinib) and Gleevec (imatinib) combination treatment demonstrated enhanced antitumor activity in patient derived xenograft models of gastrointestinal stromal tumor harboring KIT mutations (PMID: 25673643). | 25673643 |