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| Gene | KIT |
| Variant | T67S |
| Impact List | missense |
| Protein Effect | unknown |
| Gene Variant Descriptions | KIT T67S lies within Ig-like C2-type domain 1 of the Kit protein (UniProt.org). T67S has been identified in sequencing studies (PMID: 27601595), but has not been biochemically characterized and therefore, its effect on the Kit protein function is unknown (PubMed, May 2026). |
| Associated Drug Resistance | |
| Category Variants Paths |
KIT mutant KIT T67S |
| Transcript | NM_000222.3 |
| gDNA | chr4:g.54695644C>G |
| cDNA | c.200C>G |
| Protein | p.T67S |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| XM_017008180.1 | chr4:g.54695644C>G | c.200C>G | p.T67S | RefSeq | GRCh38/hg38 |
| NM_001385285.1 | chr4:g.54695644C>G | c.200C>G | p.T67S | RefSeq | GRCh38/hg38 |
| XM_017008180 | chr4:g.54695644C>G | c.200C>G | p.T67S | RefSeq | GRCh38/hg38 |
| XM_017008178.1 | chr4:g.54695644C>G | c.200C>G | p.T67S | RefSeq | GRCh38/hg38 |
| NM_001385286.1 | chr4:g.54695644C>G | c.200C>G | p.T67S | RefSeq | GRCh38/hg38 |
| NM_001385288.1 | chr4:g.54695644C>G | c.200C>G | p.T67S | RefSeq | GRCh38/hg38 |
| NM_001385292.1 | chr4:g.54695644C>G | c.200C>G | p.T67S | RefSeq | GRCh38/hg38 |
| NM_000222.3 | chr4:g.54695644C>G | c.200C>G | p.T67S | RefSeq | GRCh38/hg38 |
| NM_001385290.1 | chr4:g.54695644C>G | c.200C>G | p.T67S | RefSeq | GRCh38/hg38 |
| XM_005265742.3 | chr4:g.54695644C>G | c.200C>G | p.T67S | RefSeq | GRCh38/hg38 |
| NM_001093772.1 | chr4:g.54695644C>G | c.200C>G | p.T67S | RefSeq | GRCh38/hg38 |
| XM_005265741 | chr4:g.54695644C>G | c.200C>G | p.T67S | RefSeq | GRCh38/hg38 |
| XM_005265742 | chr4:g.54695644C>G | c.200C>G | p.T67S | RefSeq | GRCh38/hg38 |
| XM_005265740 | chr4:g.54695644C>G | c.200C>G | p.T67S | RefSeq | GRCh38/hg38 |
| XM_017008178 | chr4:g.54695644C>G | c.200C>G | p.T67S | RefSeq | GRCh38/hg38 |
| NM_000222.2 | chr4:g.54695644C>G | c.200C>G | p.T67S | RefSeq | GRCh38/hg38 |
| XM_017008179.1 | chr4:g.54695644C>G | c.200C>G | p.T67S | RefSeq | GRCh38/hg38 |
| NM_001385284.1 | chr4:g.54695644C>G | c.200C>G | p.T67S | RefSeq | GRCh38/hg38 |
| NM_001093772 | chr4:g.54695644C>G | c.200C>G | p.T67S | RefSeq | GRCh38/hg38 |
| XM_017008179 | chr4:g.54695644C>G | c.200C>G | p.T67S | RefSeq | GRCh38/hg38 |
| XM_005265741.1 | chr4:g.54695644C>G | c.200C>G | p.T67S | RefSeq | GRCh38/hg38 |
| XM_005265740.1 | chr4:g.54695644C>G | c.200C>G | p.T67S | RefSeq | GRCh38/hg38 |
| NM_001093772.2 | chr4:g.54695644C>G | c.200C>G | p.T67S | RefSeq | GRCh38/hg38 |
| NM_000222 | chr4:g.54695644C>G | c.200C>G | p.T67S | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
|---|