List of variants in gene KIT reported as uncertain significance for immune system cancer

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: 14

Download table as spreadsheet

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.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

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.