List of variants in gene KIT reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 44

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HGVS	dbSNP	gnomAD frequency
NM_000222.3(KIT):c.-14T>A	rs140909964	0.00332
NM_000222.3(KIT):c.1588G>A (p.Val530Ile)	rs72550822	0.00125
NM_000222.3(KIT):c.503C>T (p.Ala168Val)	rs149092990	0.00063
NM_000222.3(KIT):c.1195G>A (p.Val399Ile)	rs143707288	0.00059
NM_000222.3(KIT):c.1587C>T (p.Phe529=)	rs148248559	0.00049
NM_000222.3(KIT):c.200C>G (p.Thr67Ser)	rs144933028	0.00045
NM_000222.3(KIT):c.878A>G (p.Asn293Ser)	rs137909416	0.00034
NM_000222.3(KIT):c.504G>A (p.Ala168=)	rs140469176	0.00029
NM_000222.3(KIT):c.925+9C>T	rs201405378	0.00029
NM_000222.3(KIT):c.2349C>T (p.Leu783=)	rs151046591	0.00022
NM_000222.3(KIT):c.591G>A (p.Ser197=)	rs140839561	0.00022
NM_000222.3(KIT):c.251C>T (p.Thr84Met)	rs201872586	0.00019
NM_000222.3(KIT):c.1230T>C (p.Asn410=)	rs140536677	0.00017
NM_000222.3(KIT):c.1674G>A (p.Lys558=)	rs200375589	0.00016
NM_000222.3(KIT):c.1541-8C>T	rs367739763	0.00014
NM_000222.3(KIT):c.2234-3C>T	rs370131461	0.00014
NM_000222.3(KIT):c.2502G>A (p.Lys834=)	rs146992614	0.00014
NM_000222.3(KIT):c.978C>T (p.Asn326=)	rs148594615	0.00011
NM_000222.3(KIT):c.1694G>T (p.Gly565Val)	rs200945282	0.00009
NM_000222.3(KIT):c.2259T>C (p.Thr753=)	rs764287169	0.00009
NM_000222.3(KIT):c.2290C>T (p.Leu764=)	rs770413971	0.00009
NM_000222.3(KIT):c.2867G>A (p.Arg956Gln)	rs139694927	0.00008
NM_000222.3(KIT):c.2208C>T (p.Ala736=)	rs375902940	0.00006
NM_000222.3(KIT):c.522T>C (p.Ser174=)	rs145993517	0.00006
NM_000222.3(KIT):c.1848G>A (p.Ala616=)	rs148853099	0.00005
NM_000222.3(KIT):c.1296A>G (p.Gly432=)	rs781686359	0.00004
NM_000222.3(KIT):c.1991-7C>T	rs370661908	0.00004
NM_000222.3(KIT):c.2541G>A (p.Thr847=)	rs762912889	0.00004
NM_000222.3(KIT):c.2802+9A>G	rs369450271	0.00004
NM_000222.3(KIT):c.84T>C (p.Ser28=)	rs758868843	0.00004
NM_000222.3(KIT):c.-5C>T	rs202070769	0.00003
NM_000222.3(KIT):c.1404G>A (p.Pro468=)	rs767079772	0.00003
NM_000222.3(KIT):c.390C>T (p.Asn130=)	rs575926270	0.00003
NM_000222.3(KIT):c.735G>A (p.Thr245=)	rs150150449	0.00003
NM_000222.3(KIT):c.2145C>T (p.Ser715=)	rs192110951	0.00002
NM_000222.3(KIT):c.829A>G (p.Ile277Val)	rs757547974	0.00002
NM_000222.3(KIT):c.1541-5T>C	rs1722278741	0.00001
NM_000222.3(KIT):c.1800C>T (p.Phe600=)	rs138380197	0.00001
NM_000222.3(KIT):c.-9G>T
NM_000222.3(KIT):c.1155C>T (p.Thr385=)	rs373472667
NM_000222.3(KIT):c.1540+30G>A	rs886038271
NM_000222.3(KIT):c.15C>T (p.Arg5=)	rs1357038342
NM_000222.3(KIT):c.2541G>T (p.Thr847=)	rs762912889
NM_000222.3(KIT):c.33C>G (p.Leu11=)	rs894439242

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