ClinVar Miner

List of variants in gene KIT reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP
NM_000222.2(KIT):c.*1059C>T rs886059467
NM_000222.2(KIT):c.*1086C>T rs533152310
NM_000222.2(KIT):c.*1101A>G rs886059468
NM_000222.2(KIT):c.*1487_*1490delAAAA rs374796688
NM_000222.2(KIT):c.*1791G>A rs77842054
NM_000222.2(KIT):c.*1808A>G rs762662037
NM_000222.2(KIT):c.*198A>G rs886059464
NM_000222.2(KIT):c.*252G>T rs376694515
NM_000222.2(KIT):c.*352A>G rs149336515
NM_000222.2(KIT):c.*368C>T rs886059465
NM_000222.2(KIT):c.*393A>G rs886059466
NM_000222.2(KIT):c.*597C>T rs746982052
NM_000222.2(KIT):c.*790A>G rs189995563
NM_000222.2(KIT):c.-14T>A rs140909964
NM_000222.2(KIT):c.1274T>A (p.Met425Lys) rs878853760
NM_000222.2(KIT):c.200C>G (p.Thr67Ser) rs144933028
NM_000222.2(KIT):c.2670C>T (p.Leu890=) rs745967881
NM_000222.2(KIT):c.2802+9A>G rs369450271
NM_000222.2(KIT):c.2923G>C (p.Asp975His) rs373152714
NM_000222.2(KIT):c.301C>T (p.His101Tyr) rs781130745

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