ClinVar Miner

List of variants in gene KIT reported by Baylor Genetics

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Gene type:
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Total variants: 86
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HGVS dbSNP gnomAD frequency
NM_000222.3(KIT):c.1091A>G (p.Lys364Arg) rs375734891 0.00009
NM_000222.3(KIT):c.1694G>T (p.Gly565Val) rs200945282 0.00009
NM_000222.3(KIT):c.1351T>C (p.Ser451Pro) rs145183977 0.00006
NM_000222.3(KIT):c.2920G>A (p.Asp974Asn) rs72549297 0.00006
NM_000222.3(KIT):c.2293G>T (p.Asp765Tyr) rs760112920 0.00004
NM_000222.3(KIT):c.2663G>A (p.Arg888Gln) rs776681643 0.00004
NM_000222.3(KIT):c.52C>T (p.Leu18Phe) rs370787811 0.00004
NM_000222.3(KIT):c.2771T>C (p.Ile924Thr) rs1000138811 0.00003
NM_000222.3(KIT):c.463C>T (p.Pro155Ser) rs777031731 0.00003
NM_000222.3(KIT):c.944T>A (p.Ile315Asn) rs377590954 0.00003
NM_000222.3(KIT):c.1139C>T (p.Thr380Met) rs760981584 0.00002
NM_000222.3(KIT):c.1396G>A (p.Gly466Arg) rs1282859149 0.00002
NM_000222.3(KIT):c.1721C>T (p.Thr574Ile) rs1307097576 0.00002
NM_000222.3(KIT):c.2146G>A (p.Asp716Asn) rs769701248 0.00002
NM_000222.3(KIT):c.2255T>G (p.Val752Gly) rs758665590 0.00002
NM_000222.3(KIT):c.2801A>G (p.His934Arg) rs762406098 0.00002
NM_000222.3(KIT):c.2866C>T (p.Arg956Trp) rs587778433 0.00002
NM_000222.3(KIT):c.287C>T (p.Thr96Met) rs1060502564 0.00002
NM_000222.3(KIT):c.749A>G (p.Asn250Ser) rs748527429 0.00002
NM_000222.3(KIT):c.793G>A (p.Gly265Ser) rs1060502570 0.00002
NM_000222.3(KIT):c.1171A>G (p.Thr391Ala) rs757234342 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.1781C>T (p.Thr594Ile) rs375351432 0.00001
NM_000222.3(KIT):c.1789G>A (p.Ala597Thr) rs768214921 0.00001
NM_000222.3(KIT):c.1901G>A (p.Arg634Gln) rs766264502 0.00001
NM_000222.3(KIT):c.2072G>C (p.Cys691Ser) rs35200131 0.00001
NM_000222.3(KIT):c.2105T>C (p.Leu702Pro) rs541585774 0.00001
NM_000222.3(KIT):c.2107T>C (p.Tyr703His) rs746990067 0.00001
NM_000222.3(KIT):c.2198C>T (p.Pro733Leu) rs992027457 0.00001
NM_000222.3(KIT):c.2243T>C (p.Ile748Thr) rs572852980 0.00001
NM_000222.3(KIT):c.2281G>A (p.Glu761Lys) rs746503007 0.00001
NM_000222.3(KIT):c.2473G>A (p.Val825Ile) rs878853765 0.00001
NM_000222.3(KIT):c.2612C>G (p.Pro871Arg) rs755797225 0.00001
NM_000222.3(KIT):c.2621C>T (p.Pro874Leu) rs753419764 0.00001
NM_000222.3(KIT):c.2662C>T (p.Arg888Trp) rs1237984655 0.00001
NM_000222.3(KIT):c.2689G>A (p.Ala897Thr) rs1250080954 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.2882G>A (p.Gly961Asp) rs1334133798 0.00001
NM_000222.3(KIT):c.2897C>A (p.Ser966Tyr) rs765503364 0.00001
NM_000222.3(KIT):c.844G>A (p.Val282Ile) rs771961192 0.00001
NM_000222.3(KIT):c.916G>A (p.Glu306Lys) rs753258292 0.00001
NM_000222.3(KIT):c.954G>A (p.Met318Ile) rs769399180 0.00001
NM_000222.3(KIT):c.1117T>C (p.Tyr373His)
NM_000222.3(KIT):c.1183T>A (p.Ser395Thr)
NM_000222.3(KIT):c.1190C>A (p.Ser397Tyr)
NM_000222.3(KIT):c.1331C>T (p.Pro444Leu) rs774389709
NM_000222.3(KIT):c.13C>T (p.Arg5Cys)
NM_000222.3(KIT):c.1411A>C (p.Lys471Gln) rs1471406283
NM_000222.3(KIT):c.148G>A (p.Val50Met) rs200950545
NM_000222.3(KIT):c.1534A>G (p.Asn512Asp)
NM_000222.3(KIT):c.1540+3A>G rs2109769927
NM_000222.3(KIT):c.1549C>T (p.His517Tyr) rs1577994279
NM_000222.3(KIT):c.1597G>A (p.Ala533Thr) rs1722284528
NM_000222.3(KIT):c.1834A>G (p.Ile612Val)
NM_000222.3(KIT):c.1895C>T (p.Thr632Ile) rs1553891944
NM_000222.3(KIT):c.1900C>T (p.Arg634Trp) rs144369407
NM_000222.3(KIT):c.2024A>G (p.Tyr675Cys) rs764970586
NM_000222.3(KIT):c.2060A>T (p.Asp687Val)
NM_000222.3(KIT):c.2116C>T (p.Leu706Phe) rs1577998119
NM_000222.3(KIT):c.2119_2139dup (p.Leu707_Ser713dup) rs1722449916
NM_000222.3(KIT):c.2132A>G (p.Glu711Gly)
NM_000222.3(KIT):c.2261C>G (p.Pro754Arg)
NM_000222.3(KIT):c.2275G>A (p.Asp759Asn) rs754826149
NM_000222.3(KIT):c.2291T>C (p.Leu764Pro) rs1553892703
NM_000222.3(KIT):c.2294A>G (p.Asp765Gly) rs1060502545
NM_000222.3(KIT):c.22T>C (p.Trp8Arg) rs1577898533
NM_000222.3(KIT):c.2533G>A (p.Val845Ile)
NM_000222.3(KIT):c.2628T>G (p.Asp876Glu) rs778078182
NM_000222.3(KIT):c.2630C>T (p.Ser877Phe) rs1722943323
NM_000222.3(KIT):c.2683G>T (p.Ala895Ser) rs774405431
NM_000222.3(KIT):c.2731C>T (p.Pro911Ser) rs1553893575
NM_000222.3(KIT):c.2887A>G (p.Thr963Ala) rs773709702
NM_000222.3(KIT):c.2900C>T (p.Ser967Phe)
NM_000222.3(KIT):c.325G>T (p.Val109Leu)
NM_000222.3(KIT):c.340C>G (p.Pro114Ala) rs772836939
NM_000222.3(KIT):c.406T>C (p.Cys136Arg) rs1720223149
NM_000222.3(KIT):c.443T>C (p.Leu148Pro) rs1720225274
NM_000222.3(KIT):c.44T>C (p.Leu15Pro) rs1230808481
NM_000222.3(KIT):c.456G>C (p.Gln152His)
NM_000222.3(KIT):c.480G>C (p.Leu160Phe) rs1201516128
NM_000222.3(KIT):c.668T>G (p.Leu223Arg)
NM_000222.3(KIT):c.741_742delinsTG (p.Lys247_Arg248delinsAsnGly)
NM_000222.3(KIT):c.91C>A (p.Pro31Thr) rs1431394530
NM_000222.3(KIT):c.965C>A (p.Thr322Lys)

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