ClinVar Miner

List of variants in gene KIT reported as likely benign for Gastrointestinal stroma tumor

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Gene type:
ClinVar version:
Total variants: 194
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HGVS dbSNP
NM_000222.2(KIT):c.*1241G>A rs114377961
NM_000222.2(KIT):c.*149C>T rs2213181
NM_000222.2(KIT):c.*1524A>G rs17084736
NM_000222.2(KIT):c.*1704G>T rs8022
NM_000222.2(KIT):c.*217G>A rs17084733
NM_000222.2(KIT):c.1011T>C (p.Tyr337=) rs777287699
NM_000222.2(KIT):c.1017A>G (p.Ala339=) rs1253593989
NM_000222.2(KIT):c.102G>A (p.Pro34=) rs757725466
NM_000222.2(KIT):c.1032A>G (p.Glu344=) rs1553888785
NM_000222.2(KIT):c.1086T>C (p.Tyr362=) rs554090824
NM_000222.2(KIT):c.1095T>A (p.Ser365=) rs142963781
NM_000222.2(KIT):c.1098G>A (p.Glu366=) rs1060504663
NM_000222.2(KIT):c.1115+7A>G rs1553888808
NM_000222.2(KIT):c.1116-5T>C rs376229086
NM_000222.2(KIT):c.1116-9T>C rs1553889072
NM_000222.2(KIT):c.1119C>T (p.Tyr373=) rs72549293
NM_000222.2(KIT):c.1140G>A (p.Thr380=) rs766702350
NM_000222.2(KIT):c.1155C>G (p.Thr385=) rs373472667
NM_000222.2(KIT):c.1155C>T (p.Thr385=) rs373472667
NM_000222.2(KIT):c.1173A>G (p.Thr391=) rs767377458
NM_000222.2(KIT):c.1185C>A (p.Ser395=) rs755864184
NM_000222.2(KIT):c.1194C>T (p.Asp398=) rs376940990
NM_000222.2(KIT):c.1195G>A (p.Val399Ile) rs143707288
NM_000222.2(KIT):c.1206C>T (p.Ala402=) rs747686609
NM_000222.2(KIT):c.1209A>T (p.Ile403=) rs1467087033
NM_000222.2(KIT):c.1231+8A>G rs776973839
NM_000222.2(KIT):c.1232-4G>A rs759411599
NM_000222.2(KIT):c.1232-6C>G rs1553890995
NM_000222.2(KIT):c.123A>G (p.Pro41=) rs72549300
NM_000222.2(KIT):c.1254C>T (p.Tyr418=) rs1553891002
NM_000222.2(KIT):c.1257C>T (p.Asp419=) rs1165367332
NM_000222.2(KIT):c.1263C>T (p.Leu421=) rs1553891010
NM_000222.2(KIT):c.1296A>G (p.Gly432=) rs781686359
NM_000222.2(KIT):c.1296A>T (p.Gly432=) rs781686359
NM_000222.2(KIT):c.1302A>G (p.Pro434=) rs770157148
NM_000222.2(KIT):c.1317T>C (p.Asp439=) rs144185800
NM_000222.2(KIT):c.1344G>A (p.Gln448=) rs542718349
NM_000222.2(KIT):c.1346+7T>C rs199510933
NM_000222.2(KIT):c.1347-5T>C rs1553891394
NM_000222.2(KIT):c.1359T>G (p.Ser453=) rs769828541
NM_000222.2(KIT):c.1404G>A (p.Pro468=) rs767079772
NM_000222.2(KIT):c.1416A>G (p.Leu472=) rs934899537
NM_000222.2(KIT):c.1461C>G (p.Gly487=) rs1048122979
NM_000222.2(KIT):c.1464G>A (p.Thr488=) rs878853761
NM_000222.2(KIT):c.147C>T (p.Arg49=) rs72549301
NM_000222.2(KIT):c.1497G>A (p.Lys499=) rs374432699
NM_000222.2(KIT):c.1500T>C (p.Thr500=) rs1553891462
NM_000222.2(KIT):c.1506C>T (p.Ala502=) rs1060504652
NM_000222.2(KIT):c.1540+9C>A rs1553891480
NM_000222.2(KIT):c.1541-8C>T rs367739763
NM_000222.2(KIT):c.1542G>A (p.Glu514=) rs1475881614
NM_000222.2(KIT):c.156C>T (p.Asp52=) rs942280887
NM_000222.2(KIT):c.1576C>T (p.Leu526=) rs1553891660
NM_000222.2(KIT):c.1587C>T (p.Phe529=) rs148248559
NM_000222.2(KIT):c.1588G>A (p.Val530Ile) rs72550822
NM_000222.2(KIT):c.1593C>T (p.Ile531=) rs760143011
NM_000222.2(KIT):c.15C>G (p.Arg5=) rs1357038342
NM_000222.2(KIT):c.1621A>C (p.Met541Leu) rs3822214
NM_000222.2(KIT):c.1638A>G (p.Lys546=) rs55986963
NM_000222.2(KIT):c.1641T>C (p.Tyr547=) rs746718824
NM_000222.2(KIT):c.1647+7A>C rs1060504659
NM_000222.2(KIT):c.166C>T (p.Leu56=) rs1060504651
NM_000222.2(KIT):c.1674G>A (p.Lys558=) rs200375589
NM_000222.2(KIT):c.1694G>T (p.Gly565Val) rs200945282
NM_000222.2(KIT):c.1725A>G (p.Gln575=) rs1025892108
NM_000222.2(KIT):c.1761C>T (p.Asn587=) rs1553891809
NM_000222.2(KIT):c.1774+7A>G rs1310181400
NM_000222.2(KIT):c.1775-4A>G rs373072016
NM_000222.2(KIT):c.177T>C (p.Thr59=) rs1553887306
NM_000222.2(KIT):c.1794A>T (p.Gly598=) rs72549292
NM_000222.2(KIT):c.1800C>T (p.Phe600=) rs138380197
NM_000222.2(KIT):c.1803G>A (p.Gly601=) rs1060504661
NM_000222.2(KIT):c.1824T>C (p.Ala608=) rs1406480519
NM_000222.2(KIT):c.1831T>C (p.Leu611=) rs369412402
NM_000222.2(KIT):c.1848G>A (p.Ala616=) rs148853099
NM_000222.2(KIT):c.1860C>T (p.Val620=) rs200814065
NM_000222.2(KIT):c.1863T>C (p.Ala621=) rs759613218
NM_000222.2(KIT):c.1866A>G (p.Val622=) rs1287132024
NM_000222.2(KIT):c.1879+10T>C rs1553891916
NM_000222.2(KIT):c.1879+7T>C rs751507194
NM_000222.2(KIT):c.1879+8C>G rs1553891914
NM_000222.2(KIT):c.1881G>A (p.Pro627=) rs971280269
NM_000222.2(KIT):c.1893G>A (p.Leu631=) rs767511834
NM_000222.2(KIT):c.1947T>C (p.Asn649=) rs878853762
NM_000222.2(KIT):c.195A>G (p.Lys65=) rs200121443
NM_000222.2(KIT):c.1990+8C>T rs377493174
NM_000222.2(KIT):c.1990+9G>A rs757680205
NM_000222.2(KIT):c.1991-7C>T rs370661908
NM_000222.2(KIT):c.2001G>C (p.Leu667=) rs766315579
NM_000222.2(KIT):c.2016T>C (p.Tyr672=) rs1060504653
NM_000222.2(KIT):c.2050A>C (p.Arg684=) rs1553892209
NM_000222.2(KIT):c.2052A>G (p.Arg684=) rs1553892213
NM_000222.2(KIT):c.2100T>G (p.Ala700=) rs1553892249
NM_000222.2(KIT):c.2118T>G (p.Leu706=) rs766840704
NM_000222.2(KIT):c.2141+7C>T rs1360717801
NM_000222.2(KIT):c.2142-9C>T rs1553892553
NM_000222.2(KIT):c.2145C>T (p.Ser715=) rs192110951
NM_000222.2(KIT):c.2152A>G (p.Thr718Ala) rs564307874
NM_000222.2(KIT):c.2160G>A (p.Glu720=) rs372359131
NM_000222.2(KIT):c.2196C>G (p.Val732=) rs1060504655
NM_000222.2(KIT):c.2208C>A (p.Ala736=) rs375902940
NM_000222.2(KIT):c.2208C>T (p.Ala736=) rs375902940
NM_000222.2(KIT):c.222G>A (p.Thr74=) rs762453840
NM_000222.2(KIT):c.2238A>G (p.Ser746=) rs1553892658
NM_000222.2(KIT):c.2259T>C (p.Thr753=) rs764287169
NM_000222.2(KIT):c.2280C>T (p.Asp760=) rs55717477
NM_000222.2(KIT):c.2283G>A (p.Glu761=) rs1553892698
NM_000222.2(KIT):c.2290C>T (p.Leu764=) rs770413971
NM_000222.2(KIT):c.2343T>C (p.Ala781=) rs1553892716
NM_000222.2(KIT):c.2349C>T (p.Leu783=) rs151046591
NM_000222.2(KIT):c.2361+10A>G rs1214231397
NM_000222.2(KIT):c.2362-5A>C rs1060504660
NM_000222.2(KIT):c.2394C>T (p.Ile798=) rs55789615
NM_000222.2(KIT):c.2451C>T (p.Ile817=) rs1553892932
NM_000222.2(KIT):c.2493A>G (p.Leu831=) rs1553893435
NM_000222.2(KIT):c.2502G>A (p.Lys834=) rs146992614
NM_000222.2(KIT):c.251C>T (p.Thr84Met) rs201872586
NM_000222.2(KIT):c.252G>T (p.Thr84=) rs56411694
NM_000222.2(KIT):c.2535A>G (p.Val845=) rs1060504654
NM_000222.2(KIT):c.2541G>A (p.Thr847=) rs762912889
NM_000222.2(KIT):c.2541G>T (p.Thr847=) rs762912889
NM_000222.2(KIT):c.2553C>T (p.Asp851=) rs751396522
NM_000222.2(KIT):c.2577T>C (p.Leu859=) rs371058716
NM_000222.2(KIT):c.2583G>A (p.Glu861=) rs1060504662
NM_000222.2(KIT):c.2586G>C (p.Leu862=) rs3733542
NM_000222.2(KIT):c.2592T>C (p.Ser864=) rs1060504664
NM_000222.2(KIT):c.2622G>C (p.Pro874=) rs55817813
NM_000222.2(KIT):c.2625C>T (p.Val875=) rs748588125
NM_000222.2(KIT):c.2658C>T (p.Gly886=) rs1060504658
NM_000222.2(KIT):c.2670C>T (p.Leu890=) rs745967881
NM_000222.2(KIT):c.2679A>G (p.Glu893=) rs1060504657
NM_000222.2(KIT):c.2736A>G (p.Leu912=) rs761004820
NM_000222.2(KIT):c.2793C>T (p.Ser931=) rs773363866
NM_000222.2(KIT):c.2802+9A>G rs369450271
NM_000222.2(KIT):c.2826C>T (p.Cys942=) rs149932314
NM_000222.2(KIT):c.2847C>T (p.Pro949=) rs56288823
NM_000222.2(KIT):c.2850G>C (p.Val950=) rs781142513
NM_000222.2(KIT):c.2862T>C (p.Ser954=) rs1553893817
NM_000222.2(KIT):c.2880C>T (p.Val960=) rs375833392
NM_000222.2(KIT):c.2889C>T (p.Thr963=) rs200275681
NM_000222.2(KIT):c.288G>A (p.Thr96=) rs150026676
NM_000222.2(KIT):c.2901C>T (p.Ser967=) rs1553893836
NM_000222.2(KIT):c.2919C>T (p.His973=) rs755974085
NM_000222.2(KIT):c.2922C>T (p.Asp974=) rs1401923759
NM_000222.2(KIT):c.294C>T (p.Thr98=) rs959320112
NM_000222.2(KIT):c.297C>T (p.Asn99=) rs768599276
NM_000222.2(KIT):c.303C>T (p.His101=) rs145333060
NM_000222.2(KIT):c.324T>C (p.Tyr108=) rs1553887353
NM_000222.2(KIT):c.337+9T>G rs1553887358
NM_000222.2(KIT):c.338-4A>G rs878853766
NM_000222.2(KIT):c.338-4A>T rs878853766
NM_000222.2(KIT):c.363C>T (p.Asp121=) rs1553887693
NM_000222.2(KIT):c.390C>T (p.Asn130=) rs575926270
NM_000222.2(KIT):c.393C>T (p.Asp131=) rs1208138500
NM_000222.2(KIT):c.396G>A (p.Thr132=) rs149172424
NM_000222.2(KIT):c.396G>T (p.Thr132=) rs149172424
NM_000222.2(KIT):c.45C>T (p.Leu15=) rs755527973
NM_000222.2(KIT):c.501G>A (p.Lys167=) rs767567085
NM_000222.2(KIT):c.503C>T (p.Ala168Val) rs149092990
NM_000222.2(KIT):c.504G>A (p.Ala168=) rs140469176
NM_000222.2(KIT):c.516C>T (p.Ile172=) rs1060504656
NM_000222.2(KIT):c.522T>C (p.Ser174=) rs145993517
NM_000222.2(KIT):c.531C>T (p.Arg177=) rs756722358
NM_000222.2(KIT):c.543G>C (p.Arg181=) rs746419269
NM_000222.2(KIT):c.549T>C (p.Cys183=) rs1553887762
NM_000222.2(KIT):c.555T>C (p.His185=) rs1227095960
NM_000222.2(KIT):c.57C>T (p.Arg19=) rs776887125
NM_000222.2(KIT):c.588G>T (p.Leu196=) rs1060504650
NM_000222.2(KIT):c.591G>A (p.Ser197=) rs140839561
NM_000222.2(KIT):c.591G>T (p.Ser197=) rs140839561
NM_000222.2(KIT):c.600C>T (p.Phe200=) rs772105682
NM_000222.2(KIT):c.604C>T (p.Leu202=) rs759589436
NM_000222.2(KIT):c.620-10T>C rs1362563387
NM_000222.2(KIT):c.620-7A>G rs878853768
NM_000222.2(KIT):c.696G>A (p.Thr232=) rs201988161
NM_000222.2(KIT):c.696G>T (p.Thr232=) rs201988161
NM_000222.2(KIT):c.702A>G (p.Thr234=) rs1553887939
NM_000222.2(KIT):c.792C>T (p.His264=) rs753102574
NM_000222.2(KIT):c.822G>A (p.Thr274=) rs747288547
NM_000222.2(KIT):c.840G>C (p.Ala280=) rs142772432
NM_000222.2(KIT):c.84T>C (p.Ser28=) rs758868843
NM_000222.2(KIT):c.852T>C (p.Asp284=) rs1213025241
NM_000222.2(KIT):c.858A>G (p.Gly286=) rs1553888389
NM_000222.2(KIT):c.878A>G (p.Asn293Ser) rs137909416
NM_000222.2(KIT):c.882T>C (p.Asn294=) rs765997309
NM_000222.2(KIT):c.909A>C (p.Thr303=) rs531740394
NM_000222.2(KIT):c.910A>G (p.Thr304Ala) rs202052259
NM_000222.2(KIT):c.912C>T (p.Thr304=) rs999025845
NM_000222.2(KIT):c.925+9C>T rs201405378
NM_000222.2(KIT):c.952A>G (p.Met318Val) rs143388949
NM_000222.2(KIT):c.969A>G (p.Val323=) rs1553888773
NM_000222.2(KIT):c.978C>T (p.Asn326=) rs148594615
NM_000222.2(KIT):c.993A>G (p.Val331=) rs1553888778
NM_000222.2(KIT):c.9C>G (p.Gly3=) rs755780019

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