ClinVar Miner

List of variants in gene RUNX1 reported as uncertain significance by Invitae

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Gene type:
ClinVar version:
Total variants: 147
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HGVS dbSNP
NM_001001890.3(RUNX1):c.1011_1016CGGCAT[3] (p.337_338IG[3]) rs750495319
NM_001754.4(RUNX1):c.1004A>G (p.Gln335Arg)
NM_001754.4(RUNX1):c.1006T>A (p.Phe336Ile) rs756010562
NM_001754.4(RUNX1):c.1007T>C (p.Phe336Ser) rs752745196
NM_001754.4(RUNX1):c.1034C>G (p.Pro345Arg)
NM_001754.4(RUNX1):c.1035_1036dup (p.Arg346fs)
NM_001754.4(RUNX1):c.1037G>A (p.Arg346His)
NM_001754.4(RUNX1):c.1039A>G (p.Met347Val)
NM_001754.4(RUNX1):c.1041G>A (p.Met347Ile)
NM_001754.4(RUNX1):c.104G>A (p.Ser35Asn) rs1569084822
NM_001754.4(RUNX1):c.1054G>A (p.Ala352Thr) rs1397164331
NM_001754.4(RUNX1):c.105C>A (p.Ser35Arg)
NM_001754.4(RUNX1):c.105C>T (p.Ser35=) rs1569084817
NM_001754.4(RUNX1):c.1069C>T (p.Pro357Ser) rs375989348
NM_001754.4(RUNX1):c.1076C>G (p.Pro359Arg)
NM_001754.4(RUNX1):c.1082C>G (p.Thr361Ser) rs1017287894
NM_001754.4(RUNX1):c.1093G>C (p.Gly365Arg)
NM_001754.4(RUNX1):c.1107G>A (p.Ser369=)
NM_001754.4(RUNX1):c.1109C>T (p.Ala370Val) rs1457932375
NM_001754.4(RUNX1):c.1112T>C (p.Met371Thr) rs922736848
NM_001754.4(RUNX1):c.1157C>G (p.Pro386Arg) rs1569002337
NM_001754.4(RUNX1):c.1159_1161del (p.Gly387del) rs975536871
NM_001754.4(RUNX1):c.1160G>C (p.Gly387Ala) rs1238015554
NM_001754.4(RUNX1):c.1166_1186dup (p.Ser389_Pro395dup) rs1555884869
NM_001754.4(RUNX1):c.1184C>G (p.Pro395Arg) rs868527382
NM_001754.4(RUNX1):c.1184C>T (p.Pro395Leu)
NM_001754.4(RUNX1):c.1196G>C (p.Ser399Thr) rs946348885
NM_001754.4(RUNX1):c.1196G>T (p.Ser399Ile) rs946348885
NM_001754.4(RUNX1):c.1197C>A (p.Ser399Arg) rs1555884864
NM_001754.4(RUNX1):c.11A>G (p.Asp4Gly) rs534158221
NM_001754.4(RUNX1):c.1201C>T (p.Pro401Ser) rs1422877598
NM_001754.4(RUNX1):c.1202C>T (p.Pro401Leu) rs1569002142
NM_001754.4(RUNX1):c.1225G>A (p.Ala409Thr) rs1569002104
NM_001754.4(RUNX1):c.122C>T (p.Thr41Met)
NM_001754.4(RUNX1):c.1230G>A (p.Ser410=)
NM_001754.4(RUNX1):c.1232C>T (p.Ala411Val)
NM_001754.4(RUNX1):c.1234G>C (p.Gly412Arg)
NM_001754.4(RUNX1):c.1252A>G (p.Met418Val) rs578042376
NM_001754.4(RUNX1):c.1253T>G (p.Met418Arg) rs202068364
NM_001754.4(RUNX1):c.1257G>A (p.Val419=) rs1172332120
NM_001754.4(RUNX1):c.1266G>C (p.Glu422Asp) rs967317406
NM_001754.4(RUNX1):c.1268G>C (p.Arg423Pro) rs1205896319
NM_001754.4(RUNX1):c.127C>T (p.Pro43Ser) rs1555899881
NM_001754.4(RUNX1):c.1280G>T (p.Arg427Leu) rs1060502577
NM_001754.4(RUNX1):c.1283dup (p.Leu429fs) rs1555884845
NM_001754.4(RUNX1):c.1300A>G (p.Asn434Asp) rs1555884837
NM_001754.4(RUNX1):c.1301A>G (p.Asn434Ser) rs748885850
NM_001754.4(RUNX1):c.1342A>T (p.Asn448Tyr)
NM_001754.4(RUNX1):c.1354G>A (p.Val452Met) rs916623598
NM_001754.4(RUNX1):c.1381A>G (p.Asn461Asp)
NM_001754.4(RUNX1):c.1387C>T (p.Pro463Ser) rs868387185
NM_001754.4(RUNX1):c.1388C>T (p.Pro463Leu)
NM_001754.4(RUNX1):c.1396A>T (p.Met466Leu) rs762213305
NM_001754.4(RUNX1):c.13A>G (p.Ser5Gly)
NM_001754.4(RUNX1):c.1400C>A (p.Ala467Glu) rs1442794209
NM_001754.4(RUNX1):c.1403C>T (p.Pro468Leu)
NM_001754.4(RUNX1):c.1408_1409GC[4] (p.Leu472fs) rs1555884790
NM_001754.4(RUNX1):c.1416G>A (p.Leu472=) rs199733903
NM_001754.4(RUNX1):c.1418A>C (p.Glu473Ala) rs1569001446
NM_001754.4(RUNX1):c.1422G>T (p.Glu474Asp) rs886057047
NM_001754.4(RUNX1):c.155T>A (p.Met52Lys) rs200431130
NM_001754.4(RUNX1):c.156G>A (p.Met52Ile) rs1555899861
NM_001754.4(RUNX1):c.157A>G (p.Ser53Gly)
NM_001754.4(RUNX1):c.170C>G (p.Pro57Arg)
NM_001754.4(RUNX1):c.170C>T (p.Pro57Leu)
NM_001754.4(RUNX1):c.179C>T (p.Ala60Val) rs765314703
NM_001754.4(RUNX1):c.182C>T (p.Pro61Leu) rs769213771
NM_001754.4(RUNX1):c.205G>C (p.Gly69Arg) rs777168865
NM_001754.4(RUNX1):c.220G>C (p.Gly74Arg)
NM_001754.4(RUNX1):c.222C>T (p.Gly74=) rs1269069934
NM_001754.4(RUNX1):c.226C>T (p.Arg76Cys) rs1487924415
NM_001754.4(RUNX1):c.232A>T (p.Met78Leu) rs878854467
NM_001754.4(RUNX1):c.239A>C (p.Glu80Ala)
NM_001754.4(RUNX1):c.253C>A (p.His85Asn) rs121912500
NM_001754.4(RUNX1):c.259G>T (p.Gly87Cys) rs561166961
NM_001754.4(RUNX1):c.262G>C (p.Glu88Gln)
NM_001754.4(RUNX1):c.264G>C (p.Glu88Asp)
NM_001754.4(RUNX1):c.264G>T (p.Glu88Asp)
NM_001754.4(RUNX1):c.287A>G (p.Asn96Ser)
NM_001754.4(RUNX1):c.331A>G (p.Thr111Ala) rs1555899722
NM_001754.4(RUNX1):c.351+5T>C rs1555899712
NM_001754.4(RUNX1):c.35C>T (p.Ser12Leu) rs750755857
NM_001754.4(RUNX1):c.367G>C (p.Asp123His) rs373498347
NM_001754.4(RUNX1):c.369T>A (p.Asp123Glu) rs768100078
NM_001754.4(RUNX1):c.391A>G (p.Thr131Ala) rs1555898641
NM_001754.4(RUNX1):c.408T>A (p.Asn136Lys) rs1569079130
NM_001754.4(RUNX1):c.414A>T (p.Glu138Asp)
NM_001754.4(RUNX1):c.421T>G (p.Ser141Ala) rs1182543054
NM_001754.4(RUNX1):c.422C>T (p.Ser141Leu)
NM_001754.4(RUNX1):c.433A>G (p.Arg145Gly) rs757288001
NM_001754.4(RUNX1):c.445G>A (p.Ala149Thr) rs752926959
NM_001754.4(RUNX1):c.488T>G (p.Phe163Cys) rs1569078862
NM_001754.4(RUNX1):c.496C>A (p.Arg166=)
NM_001754.4(RUNX1):c.530_532dup (p.Ile177dup) rs1555894743
NM_001754.4(RUNX1):c.54G>T (p.Met18Ile)
NM_001754.4(RUNX1):c.563C>G (p.Thr188Ser) rs1343295642
NM_001754.4(RUNX1):c.56G>A (p.Arg19Lys) rs759078185
NM_001754.4(RUNX1):c.577A>G (p.Ile193Val) rs1569061812
NM_001754.4(RUNX1):c.581_586del (p.Lys194_Ile195del) rs1569061793
NM_001754.4(RUNX1):c.614-3T>C rs762247645
NM_001754.4(RUNX1):c.623A>T (p.Gln208Leu) rs777320434
NM_001754.4(RUNX1):c.641C>T (p.Thr214Ile) rs747505757
NM_001754.4(RUNX1):c.649G>A (p.Gly217Arg) rs749004431
NM_001754.4(RUNX1):c.650G>C (p.Gly217Ala) rs1372473921
NM_001754.4(RUNX1):c.657G>C (p.Leu219Phe)
NM_001754.4(RUNX1):c.667G>A (p.Glu223Lys) rs878854468
NM_001754.4(RUNX1):c.668A>G (p.Glu223Gly) rs780999703
NM_001754.4(RUNX1):c.671G>A (p.Arg224Gln)
NM_001754.4(RUNX1):c.685G>A (p.Glu229Lys)
NM_001754.4(RUNX1):c.697C>T (p.Arg233Cys) rs765528082
NM_001754.4(RUNX1):c.708G>C (p.Met236Ile) rs1060502578
NM_001754.4(RUNX1):c.70G>A (p.Gly24Arg) rs1399187182
NM_001754.4(RUNX1):c.712G>A (p.Val238Ile) rs761086208
NM_001754.4(RUNX1):c.718C>G (p.Pro240Ala) rs1569037137
NM_001754.4(RUNX1):c.733C>T (p.Pro245Ser) rs1393294594
NM_001754.4(RUNX1):c.737C>T (p.Thr246Met) rs555366994
NM_001754.4(RUNX1):c.743A>C (p.Asn248Thr) rs747748983
NM_001754.4(RUNX1):c.749G>A (p.Arg250His) rs771614642
NM_001754.4(RUNX1):c.764A>G (p.His255Arg)
NM_001754.4(RUNX1):c.770C>T (p.Thr257Ile) rs1555889935
NM_001754.4(RUNX1):c.779A>G (p.Asn260Ser) rs1569036981
NM_001754.4(RUNX1):c.787C>T (p.Pro263Ser) rs370315332
NM_001754.4(RUNX1):c.790C>G (p.Gln264Glu)
NM_001754.4(RUNX1):c.801G>A (p.Met267Ile) rs757570529
NM_001754.4(RUNX1):c.805G>C (p.Asp269His) rs1060502574
NM_001754.4(RUNX1):c.82_84del (p.Ser28del) rs775050403
NM_001754.4(RUNX1):c.832C>T (p.Pro278Ser) rs767251526
NM_001754.4(RUNX1):c.848A>G (p.Gln283Arg) rs1555885620
NM_001754.4(RUNX1):c.849G>C (p.Gln283His) rs1056623039
NM_001754.4(RUNX1):c.856C>A (p.Gln286Lys)
NM_001754.4(RUNX1):c.865G>C (p.Gly289Arg) rs1258447643
NM_001754.4(RUNX1):c.883_885del (p.Ser295del) rs771972670
NM_001754.4(RUNX1):c.899C>T (p.Thr300Met) rs758682659
NM_001754.4(RUNX1):c.917G>A (p.Arg306His) rs139336358
NM_001754.4(RUNX1):c.925G>A (p.Gly309Ser)
NM_001754.4(RUNX1):c.938T>G (p.Leu313Arg) rs766264813
NM_001754.4(RUNX1):c.939_950del (p.Ala315_Ser318del) rs748122795
NM_001754.4(RUNX1):c.969G>A (p.Thr323=)
NM_001754.4(RUNX1):c.97+4T>C rs754042987
NM_001754.4(RUNX1):c.97+4T>G rs754042987
NM_001754.4(RUNX1):c.973C>T (p.Pro325Ser)
NM_001754.4(RUNX1):c.976G>T (p.Asp326Tyr) rs1217420692
NM_001754.4(RUNX1):c.97G>A (p.Asp33Asn) rs781761402
NM_001754.4(RUNX1):c.980T>G (p.Leu327Arg) rs915447247
NM_001754.4(RUNX1):c.985G>A (p.Ala329Thr) rs1415582429
NM_001754.4(RUNX1):c.994G>A (p.Asp332Asn)
NM_001754.4(RUNX1):c.998C>G (p.Pro333Arg)

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