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KIT mutation

Deterministic view of the source YAML entity. Clinical authority remains with the cited source IDs and reviewer sign-off state.

IDBIO-KIT
TypeBiomarker
Aliases
CD117 gene mutationKIT mutation (c-KIT / CD117 gene)c-KIT mutationМутація KIT
Statusreviewed 2026-04-27 | pending_clinical_signoff
DiseasesNone declared
SourcesSRC-ESMO-MELANOMA-2024 SRC-NCCN-MELANOMA-2025 SRC-ONCOKB

Biomarker Facts

Biomarker typegene_mutation
Mutation details{"functional_impact": "Constitutive KIT tyrosine kinase activation", "gene": "KIT", "gene_hugo_id": "HGNC:6342", "hotspots": ["exon 11 deletions / insertions / point mutations (juxtamembrane — ~70% of GIST; imatinib-sensitive, best prognosis)", "exon 9 insertion (extracellular — ~10% of GIST; small-bowel; higher-dose imatinib 800 mg/day)", "D816V (exon 17, activation loop — ~95% of advanced systemic mastocytosis; imatinib-RESISTANT)", "exon 13 (V654A — secondary resistance to imatinib in GIST)"...
Measurement
MethodDNA-NGS (preferred — covers all relevant exons) OR Sanger (exon 11 + 9 + 13 + 17 directed) OR allele-specific PCR (D816V)
Unitscategorical; variant + exon + VAF reported
Sensitivity requirementD816V VAF can be very low in ASM peripheral blood — high-sensitivity ddPCR (LoD ~0.05%) preferred over Sanger
Related biomarkersBIO-PDGFRA

Notes

GIST: KIT mutation ~75–80%; PDGFRA ~10%; wild-type / SDH-deficient ~10–15%. Exon-genotype guides therapy (exon 11 → imatinib 400; exon 9 → imatinib 800 or sunitinib; D842V → avapritinib only). Advanced systemic mastocytosis: D816V drives the disease; imatinib is contraindicated in D816V (kinase-domain steric clash); midostaurin (D-RIVE), avapritinib (PATHFINDER / EXPLORER), and ripretinib (selected) are active. Mucosal / acral melanoma: ~15–20% KIT mutation — imatinib responses in exon 11 / 13 mutants.

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