List of variants in gene KIT studied for reproductive system disorder

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: 27

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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.2502G>A (p.Lys834=)	rs146992614	0.00014
NM_000222.3(KIT):c.101C>T (p.Pro34Leu)	rs55755457	0.00010
NM_000222.3(KIT):c.910A>G (p.Thr304Ala)	rs202052259	0.00006
NM_000222.3(KIT):c.2104C>G (p.Leu702Val)	rs768847037	0.00004
NM_000222.3(KIT):c.840G>C (p.Ala280=)	rs142772432	0.00004
NM_000222.3(KIT):c.182C>T (p.Pro61Leu)	rs557317141	0.00003
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.1210G>A (p.Ala404Thr)	rs1272269119	0.00001
NM_000222.3(KIT):c.1312A>G (p.Ile438Val)	rs780382854	0.00001
NM_000222.3(KIT):c.1553C>T (p.Pro518Leu)	rs569408054	0.00001
NM_000222.3(KIT):c.1951A>T (p.Met651Leu)	rs534209826	0.00001
NM_000222.3(KIT):c.2863G>T (p.Val955Leu)	rs1060502568	0.00001
NM_000222.3(KIT):c.2873A>G (p.Asn958Ser)	rs1060502563	0.00001
NM_000222.3(KIT):c.2900C>G (p.Ser967Cys)	rs1232060384	0.00001
NM_000222.3(KIT):c.531C>T (p.Arg177=)	rs756722358	0.00001
NM_000222.3(KIT):c.2294A>G (p.Asp765Gly)	rs1060502545
NM_000222.3(KIT):c.240T>A (p.Asn80Lys)	rs1553887329
NM_000222.3(KIT):c.2446G>C (p.Asp816His)	rs121913506
NM_000222.3(KIT):c.2449A>T (p.Ile817Phe)
NM_000222.3(KIT):c.2564A>G (p.Tyr855Cys)	rs1722933723
NM_000222.3(KIT):c.2887A>G (p.Thr963Ala)	rs773709702
NM_000222.3(KIT):c.302A>G (p.His101Arg)	rs1274601103
NM_000222.3(KIT):c.867G>C (p.Met289Ile)	rs1297145844

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