ClinVar Miner

List of variants in gene HNF1A reported as uncertain significance for not provided

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Gene type:
ClinVar version:
Total variants: 215
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HGVS dbSNP gnomAD frequency
NM_000545.8(HNF1A):c.1748G>A (p.Arg583Gln) rs137853242 0.00060
NC_000012.12:g.120978302C>T rs1039479235 0.00029
NM_000545.8(HNF1A):c.1541A>G (p.His514Arg) rs202039659 0.00028
NM_000545.8(HNF1A):c.1309+102A>T rs113111047 0.00018
NM_000545.8(HNF1A):c.524A>G (p.Gln175Arg) rs147400498 0.00018
NM_000545.8(HNF1A):c.1756G>A (p.Ala586Thr) rs373857078 0.00017
NM_000545.8(HNF1A):c.716C>T (p.Ala239Val) rs587778397 0.00016
NC_000012.12:g.120978511A>G rs756136537 0.00015
NM_000545.8(HNF1A):c.521C>T (p.Ala174Val) rs201934320 0.00013
NM_000545.8(HNF1A):c.1706G>A (p.Ser569Asn) rs752219487 0.00011
NM_000545.8(HNF1A):c.142G>A (p.Glu48Lys) rs772222326 0.00009
NM_000545.8(HNF1A):c.1721G>A (p.Ser574Asn) rs773895173 0.00009
NM_000545.8(HNF1A):c.-181G>A rs980850048 0.00007
NM_000545.8(HNF1A):c.341G>A (p.Arg114His) rs139016696 0.00007
NM_000545.8(HNF1A):c.1061C>T (p.Thr354Met) rs757068809 0.00006
NM_000545.8(HNF1A):c.1405C>T (p.His469Tyr) rs201811844 0.00006
NM_000545.8(HNF1A):c.245C>T (p.Thr82Met) rs568123980 0.00006
NM_000545.8(HNF1A):c.481G>A (p.Ala161Thr) rs201095611 0.00004
NM_000545.8(HNF1A):c.527-18G>A rs375259151 0.00004
NM_000545.8(HNF1A):c.962G>A (p.Arg321His) rs751761766 0.00004
NM_000545.8(HNF1A):c.1322C>A (p.Thr441Lys) rs371544082 0.00003
NM_000545.8(HNF1A):c.139G>C (p.Gly47Arg) rs373180062 0.00003
NM_000545.8(HNF1A):c.467C>T (p.Thr156Met) rs150513055 0.00003
NM_000545.8(HNF1A):c.125G>A (p.Gly42Asp) rs1261968643 0.00002
NM_000545.8(HNF1A):c.1274C>T (p.Thr425Met) rs1401743626 0.00002
NM_000545.8(HNF1A):c.1504C>G (p.Leu502Val) rs924150546 0.00002
NM_000545.8(HNF1A):c.1745A>G (p.His582Arg) rs193922589 0.00002
NM_000545.8(HNF1A):c.29C>T (p.Thr10Met) rs774637975 0.00002
NM_000545.8(HNF1A):c.923C>T (p.Pro308Leu) rs754306821 0.00002
NC_000012.12:g.120978493A>G rs1876057794 0.00001
NM_000545.8(HNF1A):c.1030G>A (p.Val344Met) rs767616383 0.00001
NM_000545.8(HNF1A):c.127C>A (p.Pro43Thr) rs749730441 0.00001
NM_000545.8(HNF1A):c.1478T>C (p.Met493Thr) rs1002380887 0.00001
NM_000545.8(HNF1A):c.1494C>A (p.Ser498Arg) rs138145827 0.00001
NM_000545.8(HNF1A):c.1513C>A (p.His505Asn) rs577078110 0.00001
NM_000545.8(HNF1A):c.1537A>T (p.Thr513Ser) rs753702603 0.00001
NM_000545.8(HNF1A):c.1555C>T (p.Pro519Ser) rs200639058 0.00001
NM_000545.8(HNF1A):c.1573A>T (p.Thr525Ser) rs759717253 0.00001
NM_000545.8(HNF1A):c.1637A>C (p.Asp546Ala) rs984428675 0.00001
NM_000545.8(HNF1A):c.1660G>A (p.Gly554Arg) rs752230220 0.00001
NM_000545.8(HNF1A):c.1663C>T (p.Leu555Phe) rs193922587 0.00001
NM_000545.8(HNF1A):c.1699G>A (p.Val567Ile) rs751368921 0.00001
NM_000545.8(HNF1A):c.1768G>A (p.Val590Met) rs1168108747 0.00001
NM_000545.8(HNF1A):c.203G>A (p.Arg68Gln) rs188085301 0.00001
NM_000545.8(HNF1A):c.340C>T (p.Arg114Cys) rs774996577 0.00001
NM_000545.8(HNF1A):c.503G>A (p.Arg168His) rs377110124 0.00001
NM_000545.8(HNF1A):c.50T>A (p.Leu17His) rs1480672278 0.00001
NM_000545.8(HNF1A):c.527-19C>T rs563495098 0.00001
NM_000545.8(HNF1A):c.766T>A (p.Ser256Thr) rs781711191 0.00001
NM_000545.8(HNF1A):c.775G>A (p.Val259Ile) rs778074427 0.00001
NM_000545.8(HNF1A):c.824A>C (p.Glu275Ala) rs199890776 0.00001
NM_000545.8(HNF1A):c.865C>A (p.Pro289Thr) rs765829022 0.00001
NM_000545.8(HNF1A):c.884C>T (p.Pro295Leu) rs747958319 0.00001
NM_000545.8(HNF1A):c.901G>A (p.Ala301Thr) rs555681479 0.00001
NC_000012.12:g.120978487A>G
NM_000545.8(HNF1A):c.-119del rs754470733
NM_000545.8(HNF1A):c.-124G>A rs563304627
NM_000545.8(HNF1A):c.-124G>C rs563304627
NM_000545.8(HNF1A):c.-167TGGGGGT[3] rs538476099
NM_000545.8(HNF1A):c.-61G>A
NM_000545.8(HNF1A):c.-62C>G
NM_000545.8(HNF1A):c.100G>A (p.Gly34Arg)
NM_000545.8(HNF1A):c.1064G>T (p.Gly355Val) rs2135845325
NM_000545.8(HNF1A):c.1087C>G (p.Leu363Val)
NM_000545.8(HNF1A):c.1108G>T (p.Val370Phe) rs2135845768
NM_000545.8(HNF1A):c.1114G>A (p.Ala372Thr) rs587780356
NM_000545.8(HNF1A):c.1123G>A (p.Gly375Ser)
NM_000545.8(HNF1A):c.1124G>A (p.Gly375Asp)
NM_000545.8(HNF1A):c.1126C>T (p.Pro376Ser)
NM_000545.8(HNF1A):c.1135C>A (p.Pro379Thr) rs754729248
NM_000545.8(HNF1A):c.1135C>G (p.Pro379Ala) rs754729248
NM_000545.8(HNF1A):c.1135C>T (p.Pro379Ser)
NM_000545.8(HNF1A):c.1136C>A (p.Pro379His) rs371717826
NM_000545.8(HNF1A):c.1190A>G (p.Asn397Ser) rs765239803
NM_000545.8(HNF1A):c.1197G>C (p.Gln399His)
NM_000545.8(HNF1A):c.1231G>A (p.Val411Ile)
NM_000545.8(HNF1A):c.1231G>T (p.Val411Phe) rs767284188
NM_000545.8(HNF1A):c.1293C>T (p.Ala431=)
NM_000545.8(HNF1A):c.1322C>T (p.Thr441Met)
NM_000545.8(HNF1A):c.1343TCA[1] (p.Ile449del)
NM_000545.8(HNF1A):c.1380_1406del (p.Gln460_Leu468del) rs544842497
NM_000545.8(HNF1A):c.1384G>A (p.Val462Ile)
NM_000545.8(HNF1A):c.1406A>T (p.His469Leu)
NM_000545.8(HNF1A):c.1424C>T (p.Pro475Leu) rs193922580
NM_000545.8(HNF1A):c.1431G>A (p.Met477Ile)
NM_000545.8(HNF1A):c.1438G>A (p.Val480Met)
NM_000545.8(HNF1A):c.1448A>G (p.His483Arg)
NM_000545.8(HNF1A):c.1501+5G>C rs1399164820
NM_000545.8(HNF1A):c.1505T>A (p.Leu502His) rs2135850526
NM_000545.8(HNF1A):c.1524G>T (p.Glu508Asp) rs1877291173
NM_000545.8(HNF1A):c.152G>A (p.Gly51Asp) rs776710848
NM_000545.8(HNF1A):c.1531C>G (p.Gln511Glu) rs551484245
NM_000545.8(HNF1A):c.1556C>G (p.Pro519Arg)
NM_000545.8(HNF1A):c.1566G>T (p.Met522Ile) rs2135850753
NM_000545.8(HNF1A):c.1576G>T (p.Asp526Tyr)
NM_000545.8(HNF1A):c.1583C>G (p.Thr528Ser)
NM_000545.8(HNF1A):c.1594G>A (p.Ala532Thr) rs1421619915
NM_000545.8(HNF1A):c.1605C>A (p.Ser535Arg) rs758034834
NM_000545.8(HNF1A):c.1610C>G (p.Thr537Arg)
NM_000545.8(HNF1A):c.1610C>T (p.Thr537Met) rs372624970
NM_000545.8(HNF1A):c.1613C>T (p.Pro538Leu) rs2135850924
NM_000545.8(HNF1A):c.1623G>T (p.Gln541His)
NM_000545.8(HNF1A):c.1624-3C>T
NM_000545.8(HNF1A):c.1655A>G (p.Glu552Gly)
NM_000545.8(HNF1A):c.1661G>C (p.Gly554Ala)
NM_000545.8(HNF1A):c.1703C>T (p.Pro568Leu)
NM_000545.8(HNF1A):c.1715C>A (p.Pro572His) rs2135851502
NM_000545.8(HNF1A):c.1716_1718del (p.Ala573del)
NM_000545.8(HNF1A):c.1747C>G (p.Arg583Gly) rs137853239
NM_000545.8(HNF1A):c.1754G>C (p.Ser585Thr)
NM_000545.8(HNF1A):c.1762C>T (p.Pro588Ser) rs1029590003
NM_000545.8(HNF1A):c.1768+4A>G
NM_000545.8(HNF1A):c.17G>T (p.Ser6Ile) rs2135819354
NM_000545.8(HNF1A):c.181C>T (p.Pro61Ser)
NM_000545.8(HNF1A):c.1883C>G (p.Ser628Cys)
NM_000545.8(HNF1A):c.196_198dup (p.Glu66_Thr67insGlu)
NM_000545.8(HNF1A):c.206G>A (p.Gly69Asp) rs758774357
NM_000545.8(HNF1A):c.217G>A (p.Glu73Lys)
NM_000545.8(HNF1A):c.221C>T (p.Thr74Met)
NM_000545.8(HNF1A):c.225C>A (p.Asp75Glu) rs202180554
NM_000545.8(HNF1A):c.239A>T (p.Asp80Val)
NM_000545.8(HNF1A):c.242T>C (p.Phe81Ser) rs1565880245
NM_000545.8(HNF1A):c.247C>G (p.Pro83Ala) rs1201174446
NM_000545.8(HNF1A):c.251C>T (p.Pro84Leu)
NM_000545.8(HNF1A):c.259A>C (p.Lys87Gln)
NM_000545.8(HNF1A):c.26A>G (p.Gln9Arg) rs1876081310
NM_000545.8(HNF1A):c.283G>A (p.Glu95Lys) rs1555210473
NM_000545.8(HNF1A):c.283G>C (p.Glu95Gln) rs1555210473
NM_000545.8(HNF1A):c.290C>A (p.Ala97Glu) rs374794304
NM_000545.8(HNF1A):c.290C>T (p.Ala97Val)
NM_000545.8(HNF1A):c.311_316dup (p.Glu105_Thr106insMetGlu)
NM_000545.8(HNF1A):c.317C>A (p.Thr106Asn)
NM_000545.8(HNF1A):c.332A>G (p.Asp111Gly)
NM_000545.8(HNF1A):c.332A>T (p.Asp111Val)
NM_000545.8(HNF1A):c.34C>G (p.Leu12Val) rs1275805852
NM_000545.8(HNF1A):c.353T>C (p.Met118Thr)
NM_000545.8(HNF1A):c.354G>A (p.Met118Ile)
NM_000545.8(HNF1A):c.355G>A (p.Val119Ile) rs1179591039
NM_000545.8(HNF1A):c.361T>C (p.Ser121Pro) rs2135832515
NM_000545.8(HNF1A):c.367C>G (p.Leu123Val) rs1876669134
NM_000545.8(HNF1A):c.369GCA[4] (p.Gln125dup) rs193922596
NM_000545.8(HNF1A):c.379A>G (p.Asn127Asp)
NM_000545.8(HNF1A):c.382A>G (p.Ile128Val) rs1876669657
NM_000545.8(HNF1A):c.401_406dup (p.Asp135_Thr136insIleAsp) rs2135832623
NM_000545.8(HNF1A):c.428A>G (p.His143Arg)
NM_000545.8(HNF1A):c.43G>T (p.Ala15Ser) rs1265717222
NM_000545.8(HNF1A):c.441C>A (p.His147Gln) rs193922597
NM_000545.8(HNF1A):c.445A>G (p.Asn149Asp) rs1565883574
NM_000545.8(HNF1A):c.458C>A (p.Pro153His)
NM_000545.8(HNF1A):c.458C>T (p.Pro153Leu)
NM_000545.8(HNF1A):c.461T>C (p.Met154Thr) rs2135832753
NM_000545.8(HNF1A):c.461T>G (p.Met154Arg)
NM_000545.8(HNF1A):c.462G>T (p.Met154Ile)
NM_000545.8(HNF1A):c.467C>A (p.Thr156Lys) rs150513055
NM_000545.8(HNF1A):c.472A>G (p.Lys158Glu)
NM_000545.8(HNF1A):c.490A>C (p.Thr164Pro) rs772597940
NM_000545.8(HNF1A):c.494G>T (p.Trp165Leu)
NM_000545.8(HNF1A):c.4G>A (p.Val2Ile) rs1876080206
NM_000545.8(HNF1A):c.502C>T (p.Arg168Cys)
NM_000545.8(HNF1A):c.507G>A (p.Lys169=)
NM_000545.8(HNF1A):c.509A>C (p.Gln170Pro)
NM_000545.8(HNF1A):c.512G>A (p.Arg171Gln)
NM_000545.8(HNF1A):c.514G>C (p.Glu172Gln)
NM_000545.8(HNF1A):c.518T>C (p.Val173Ala)
NM_000545.8(HNF1A):c.526+2dup rs1555211448
NM_000545.8(HNF1A):c.528G>C (p.Gln176His)
NM_000545.8(HNF1A):c.565C>T (p.Pro189Ser)
NM_000545.8(HNF1A):c.599G>T (p.Arg200Leu)
NM_000545.8(HNF1A):c.608G>T (p.Arg203Leu) rs587780357
NM_000545.8(HNF1A):c.629C>T (p.Ser210Phe) rs2135839404
NM_000545.8(HNF1A):c.644T>C (p.Phe215Ser) rs2135839510
NM_000545.8(HNF1A):c.649G>C (p.Ala217Pro)
NM_000545.8(HNF1A):c.670C>G (p.Pro224Ala) rs193922600
NM_000545.8(HNF1A):c.685C>G (p.Arg229Gly) rs769086289
NM_000545.8(HNF1A):c.691A>T (p.Thr231Ser)
NM_000545.8(HNF1A):c.698T>C (p.Val233Ala)
NM_000545.8(HNF1A):c.700G>A (p.Glu234Lys) rs2135839920
NM_000545.8(HNF1A):c.706T>G (p.Cys236Gly)
NM_000545.8(HNF1A):c.711T>G (p.Asn237Lys)
NM_000545.8(HNF1A):c.713+4C>A
NM_000545.8(HNF1A):c.714-3del
NM_000545.8(HNF1A):c.716C>A (p.Ala239Glu) rs587778397
NM_000545.8(HNF1A):c.717G>A (p.Ala239=)
NM_000545.8(HNF1A):c.722G>A (p.Cys241Tyr) rs2135841113
NM_000545.8(HNF1A):c.731G>T (p.Arg244Ile) rs193922602
NM_000545.8(HNF1A):c.734G>T (p.Gly245Val) rs193922603
NM_000545.8(HNF1A):c.736G>A (p.Val246Met)
NM_000545.8(HNF1A):c.740C>T (p.Ser247Phe)
NM_000545.8(HNF1A):c.761T>C (p.Leu254Pro)
NM_000545.8(HNF1A):c.769A>C (p.Asn257His)
NM_000545.8(HNF1A):c.772C>G (p.Leu258Val) rs1186303503
NM_000545.8(HNF1A):c.778A>G (p.Thr260Ala)
NM_000545.8(HNF1A):c.794A>C (p.Tyr265Ser) rs1555212006
NM_000545.8(HNF1A):c.797A>G (p.Asn266Ser) rs2135841726
NM_000545.8(HNF1A):c.79_80delinsCC (p.Ile27Pro) rs2135819573
NM_000545.8(HNF1A):c.800G>C (p.Trp267Ser)
NM_000545.8(HNF1A):c.802T>C (p.Phe268Leu) rs2135841769
NM_000545.8(HNF1A):c.805G>A (p.Ala269Thr) rs1426548804
NM_000545.8(HNF1A):c.818AAG[2] (p.Glu275del) rs1288094664
NM_000545.8(HNF1A):c.848T>C (p.Met283Thr)
NM_000545.8(HNF1A):c.850G>A (p.Asp284Asn)
NM_000545.8(HNF1A):c.862G>A (p.Gly288Arg)
NM_000545.8(HNF1A):c.865C>T (p.Pro289Ser) rs765829022
NM_000545.8(HNF1A):c.866C>G (p.Pro289Arg) rs267603343
NM_000545.8(HNF1A):c.866C>T (p.Pro289Leu) rs267603343
NM_000545.8(HNF1A):c.869C>A (p.Pro290His) rs778231679
NM_000545.8(HNF1A):c.871C>A (p.Pro291Thr) rs151256267
NM_000545.8(HNF1A):c.871C>G (p.Pro291Ala) rs151256267
NM_000545.8(HNF1A):c.872C>A (p.Pro291Gln) rs193922606
NM_000545.8(HNF1A):c.872C>G (p.Pro291Arg) rs193922606
NM_000545.8(HNF1A):c.89T>C (p.Leu30Pro)
NM_000545.8(HNF1A):c.917G>T (p.Gly306Val)
NM_000545.8(HNF1A):c.944G>A (p.Ser315Asn) rs1298749678
NM_000545.8(HNF1A):c.961C>T (p.Arg321Cys)
NM_000545.8(HNF1A):c.979A>G (p.Thr327Ala)

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