List of variants in gene KIT reported by St. Jude Molecular Pathology, St. Jude Children's Research Hospital

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000222.3(KIT):c.200C>G (p.Thr67Ser)	rs144933028	0.00045
NM_000222.3(KIT):c.101C>T (p.Pro34Leu)	rs55755457	0.00010
NM_000222.3(KIT):c.2867G>A (p.Arg956Gln)	rs139694927	0.00008
NM_000222.3(KIT):c.2920G>A (p.Asp974Asn)	rs72549297	0.00006
NM_000222.3(KIT):c.910A>G (p.Thr304Ala)	rs202052259	0.00006
NM_000222.3(KIT):c.391G>A (p.Asp131Asn)	rs1044091916	0.00004
NM_000222.3(KIT):c.2621C>T (p.Pro874Leu)	rs753419764	0.00001
NM_000222.3(KIT):c.124G>A (p.Gly42Arg)
NM_000222.3(KIT):c.1412A>C (p.Lys471Thr)
NM_000222.3(KIT):c.1670G>A (p.Trp557Ter)	rs1057520032
NM_000222.3(KIT):c.340C>G (p.Pro114Ala)	rs772836939

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