List of variants in gene KIT reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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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.2104C>G (p.Leu702Val)	rs768847037	0.00004
NM_000222.3(KIT):c.2881G>A (p.Gly961Ser)	rs773828910	0.00003
NM_000222.3(KIT):c.2057G>A (p.Arg686His)	rs143772138	0.00002
NM_000222.3(KIT):c.2836C>T (p.Arg946Ter)	rs139000082	0.00002
NM_000222.3(KIT):c.2866C>T (p.Arg956Trp)	rs587778433	0.00002
NM_000222.3(KIT):c.1553C>T (p.Pro518Leu)	rs569408054	0.00001
NM_000222.3(KIT):c.2863G>T (p.Val955Leu)	rs1060502568	0.00001
NM_000222.3(KIT):c.2900C>G (p.Ser967Cys)	rs1232060384	0.00001
NM_000222.3(KIT):c.2294A>G (p.Asp765Gly)	rs1060502545
NM_000222.3(KIT):c.2887A>G (p.Thr963Ala)	rs773709702
NM_000222.3(KIT):c.302A>G (p.His101Arg)	rs1274601103

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