ClinVar Miner

List of variants in gene HNF1A studied for Monogenic diabetes

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Gene type:
ClinVar version:
Total variants: 311
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HGVS dbSNP gnomAD frequency
NM_000545.8(HNF1A):c.1720A>G (p.Ser574Gly) rs1169305 0.98610
NM_000545.8(HNF1A):c.293C>T (p.Ala98Val) rs1800574 0.02065
NM_000545.8(HNF1A):c.1165T>G (p.Leu389Val) rs115080759 0.00198
NM_000545.8(HNF1A):c.1722C>A (p.Ser574Arg) rs141304623 0.00103
NM_000545.8(HNF1A):c.92G>A (p.Gly31Asp) rs137853247 0.00076
NM_000545.8(HNF1A):c.965A>G (p.Tyr322Cys) rs140491072 0.00041
NM_000545.8(HNF1A):c.1541A>G (p.His514Arg) rs202039659 0.00028
NM_000545.8(HNF1A):c.-258A>G rs756136537 0.00015
NM_000545.8(HNF1A):c.185A>G (p.Asn62Ser) rs377129682 0.00010
NM_000545.8(HNF1A):c.142G>A (p.Glu48Lys) rs772222326 0.00009
NM_000545.8(HNF1A):c.225C>T (p.Asp75=) rs202180554 0.00009
NM_000545.8(HNF1A):c.42G>A (p.Ala14=) rs775391034 0.00007
NM_000545.8(HNF1A):c.871C>T (p.Pro291Ser) rs151256267 0.00006
NM_000545.8(HNF1A):c.1383C>T (p.Pro461=) rs772756175 0.00004
NM_000545.8(HNF1A):c.-6C>T rs779387337 0.00003
NM_000545.8(HNF1A):c.139G>C (p.Gly47Arg) rs373180062 0.00003
NM_000545.8(HNF1A):c.1522G>A (p.Glu508Lys) rs483353044 0.00003
NM_000545.8(HNF1A):c.30G>A (p.Thr10=) rs746020457 0.00003
NM_000545.8(HNF1A):c.467C>T (p.Thr156Met) rs150513055 0.00003
NM_000545.8(HNF1A):c.827C>G (p.Ala276Gly) rs137853245 0.00003
NM_000545.8(HNF1A):c.1504C>G (p.Leu502Val) rs924150546 0.00002
NM_000545.8(HNF1A):c.1592G>C (p.Ser531Thr) rs137853246 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.833G>A (p.Arg278Gln) rs760640415 0.00002
NM_000545.8(HNF1A):c.-187C>T rs970766228 0.00001
NM_000545.8(HNF1A):c.-218T>C rs1024131753 0.00001
NM_000545.8(HNF1A):c.1136C>G (p.Pro379Arg) rs371717826 0.00001
NM_000545.8(HNF1A):c.1340C>T (p.Pro447Leu) rs137853236 0.00001
NM_000545.8(HNF1A):c.140G>A (p.Gly47Glu) rs1391743259 0.00001
NM_000545.8(HNF1A):c.1513C>A (p.His505Asn) rs577078110 0.00001
NM_000545.8(HNF1A):c.1521C>A (p.Pro507=) rs977750039 0.00001
NM_000545.8(HNF1A):c.1556C>T (p.Pro519Leu) rs749673816 0.00001
NM_000545.8(HNF1A):c.1663C>T (p.Leu555Phe) rs193922587 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.257T>A (p.Leu86His) rs200442958 0.00001
NM_000545.8(HNF1A):c.50T>A (p.Leu17His) rs1480672278 0.00001
NM_000545.8(HNF1A):c.557T>C (p.Ile186Thr) rs587778396 0.00001
NM_000545.8(HNF1A):c.599G>A (p.Arg200Gln) rs893256143 0.00001
NM_000545.8(HNF1A):c.608G>A (p.Arg203His) rs587780357 0.00001
NM_000545.8(HNF1A):c.626C>A (p.Ala209Glu) rs1286294151 0.00001
NM_000545.8(HNF1A):c.766T>A (p.Ser256Thr) rs781711191 0.00001
NM_000545.8(HNF1A):c.812G>A (p.Arg271Gln) rs779184183 0.00001
NG_011731.2:g.4741A>C rs2135818776
NM_000545.5(HNF1A):c.598C>T (p.Arg200Trp) rs193922598
NM_000545.8(HNF1A):c.-167TGGGGGT[3] rs538476099
NM_000545.8(HNF1A):c.-187C>A rs970766228
NM_000545.8(HNF1A):c.1114G>A (p.Ala372Thr) rs587780356
NM_000545.8(HNF1A):c.1129del (p.Leu377fs) rs193922576
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.1136C>A (p.Pro379His) rs371717826
NM_000545.8(HNF1A):c.1137del (p.Val380fs) rs1555212248
NM_000545.8(HNF1A):c.1137dup (p.Val380fs) rs2135845908
NM_000545.8(HNF1A):c.1168G>C (p.Glu390Gln) rs1877115047
NM_000545.8(HNF1A):c.121G>T (p.Glu41Ter) rs2135819670
NM_000545.8(HNF1A):c.1265T>C (p.Leu422Pro) rs193922577
NM_000545.8(HNF1A):c.1295C>A (p.Ser432Tyr)
NM_000545.8(HNF1A):c.1295C>G (p.Ser432Cys)
NM_000545.8(HNF1A):c.1295C>T (p.Ser432Phe)
NM_000545.8(HNF1A):c.129_130delinsA (p.Leu44fs) rs2135819704
NM_000545.8(HNF1A):c.130del (p.Leu44fs) rs193922578
NM_000545.8(HNF1A):c.1359del (p.Ser454fs) rs1555212359
NM_000545.8(HNF1A):c.137A>C (p.Lys46Thr) rs2135819731
NM_000545.8(HNF1A):c.139G>A (p.Gly47Arg) rs373180062
NM_000545.8(HNF1A):c.1424C>T (p.Pro475Leu) rs193922580
NM_000545.8(HNF1A):c.142del (p.Glu48fs) rs1566092470
NM_000545.8(HNF1A):c.1481C>T (p.Ala494Val)
NM_000545.8(HNF1A):c.1489C>T (p.Gln497Ter) rs1555212396
NM_000545.8(HNF1A):c.14T>G (p.Leu5Arg) rs188016232
NM_000545.8(HNF1A):c.1501+1G>A rs1131692182
NM_000545.8(HNF1A):c.1501+1G>T rs1131692182
NM_000545.8(HNF1A):c.1501+5G>C rs1399164820
NM_000545.8(HNF1A):c.1505T>A (p.Leu502His) rs2135850526
NM_000545.8(HNF1A):c.1506_1507dup (p.Tyr503fs) rs193922582
NM_000545.8(HNF1A):c.152G>T (p.Gly51Val) rs776710848
NM_000545.8(HNF1A):c.1544C>A (p.Thr515Lys) rs745460046
NM_000545.8(HNF1A):c.1544C>T (p.Thr515Met) rs745460046
NM_000545.8(HNF1A):c.1548C>T (p.Gly516=) rs886038346
NM_000545.8(HNF1A):c.155_156delinsCT (p.Gly52Ala) rs587778393
NM_000545.8(HNF1A):c.1576G>T (p.Asp526Tyr)
NM_000545.8(HNF1A):c.160C>T (p.Arg54Ter) rs766956862
NM_000545.8(HNF1A):c.1623+1G>A rs2135850957
NM_000545.8(HNF1A):c.1623+3A>G rs886038347
NM_000545.8(HNF1A):c.164_168del (p.Gly55fs) rs2135819834
NM_000545.8(HNF1A):c.169del (p.Leu57fs) rs193922588
NM_000545.8(HNF1A):c.16A>T (p.Ser6Cys) rs2135819349
NM_000545.8(HNF1A):c.1719del (p.Ser574fs) rs2135851518
NM_000545.8(HNF1A):c.1720_1733delinsGGCATCCAGCACC (p.Ser574fs) rs587778399
NM_000545.8(HNF1A):c.1768+11C>T rs886049034
NM_000545.8(HNF1A):c.1768+1G>A rs1877324101
NM_000545.8(HNF1A):c.1768+65dup rs193922590
NM_000545.8(HNF1A):c.17G>A (p.Ser6Asn) rs2135819354
NM_000545.8(HNF1A):c.185del (p.Asn62fs) rs2135819895
NM_000545.8(HNF1A):c.186del (p.Asn62fs) rs2135819908
NM_000545.8(HNF1A):c.194G>A (p.Gly65Glu) rs2135819938
NM_000545.8(HNF1A):c.196dup (p.Glu66fs) rs2135819929
NM_000545.8(HNF1A):c.19C>T (p.Gln7Ter) rs1566092307
NM_000545.8(HNF1A):c.1A>C (p.Met1Leu) rs193922592
NM_000545.8(HNF1A):c.1A>G (p.Met1Val) rs193922592
NM_000545.8(HNF1A):c.1A>T (p.Met1Leu) rs193922592
NM_000545.8(HNF1A):c.202C>T (p.Arg68Trp) rs779442858
NM_000545.8(HNF1A):c.206del (p.Gly69fs) rs2135819979
NM_000545.8(HNF1A):c.217G>T (p.Glu73Ter) rs905788991
NM_000545.8(HNF1A):c.225C>A (p.Asp75Glu) rs202180554
NM_000545.8(HNF1A):c.225C>G (p.Asp75Glu) rs202180554
NM_000545.8(HNF1A):c.22C>A (p.Leu8Met) rs2135819378
NM_000545.8(HNF1A):c.24_35dup (p.Gln9_Leu12dup) rs2135819368
NM_000545.8(HNF1A):c.259A>T (p.Lys87Ter) rs2135820197
NM_000545.8(HNF1A):c.25C>T (p.Gln9Ter) rs2135819387
NM_000545.8(HNF1A):c.26A>C (p.Gln9Pro) rs1876081310
NM_000545.8(HNF1A):c.26A>G (p.Gln9Arg) rs1876081310
NM_000545.8(HNF1A):c.281C>T (p.Pro94Leu) rs193922593
NM_000545.8(HNF1A):c.282dup (p.Glu95Ter) rs2135820267
NM_000545.8(HNF1A):c.28A>C (p.Thr10Pro) rs2135819400
NM_000545.8(HNF1A):c.2T>C (p.Met1Thr) rs2135819325
NM_000545.8(HNF1A):c.306C>T (p.Ala102=) rs1486966222
NM_000545.8(HNF1A):c.313dup (p.Glu105fs) rs193922594
NM_000545.8(HNF1A):c.319C>A (p.Leu107Ile) rs2135820404
NM_000545.8(HNF1A):c.319C>G (p.Leu107Val)
NM_000545.8(HNF1A):c.320T>C (p.Leu107Pro) rs2135820413
NM_000545.8(HNF1A):c.320T>G (p.Leu107Arg) rs2135820413
NM_000545.8(HNF1A):c.323T>C (p.Leu108Pro) rs2135820418
NM_000545.8(HNF1A):c.326+1G>A rs2135820424
NM_000545.8(HNF1A):c.326+1G>C rs2135820424
NM_000545.8(HNF1A):c.326+1G>T rs2135820424
NM_000545.8(HNF1A):c.326+2T>G rs1555210478
NM_000545.8(HNF1A):c.326+2dup rs2135820427
NM_000545.8(HNF1A):c.326+4A>G rs193922595
NM_000545.8(HNF1A):c.327-14T>C rs886049033
NM_000545.8(HNF1A):c.327-1G>A
NM_000545.8(HNF1A):c.327-1G>T rs2135832426
NM_000545.8(HNF1A):c.327-2A>T rs2135832423
NM_000545.8(HNF1A):c.332A>G (p.Asp111Gly)
NM_000545.8(HNF1A):c.335C>T (p.Pro112Leu) rs137853243
NM_000545.8(HNF1A):c.342dup (p.Val115fs) rs2135832474
NM_000545.8(HNF1A):c.34C>G (p.Leu12Val) rs1275805852
NM_000545.8(HNF1A):c.34C>T (p.Leu12Phe) rs1275805852
NM_000545.8(HNF1A):c.358A>G (p.Lys120Glu)
NM_000545.8(HNF1A):c.35T>A (p.Leu12His) rs2135819422
NM_000545.8(HNF1A):c.35T>C (p.Leu12Pro) rs2135819422
NM_000545.8(HNF1A):c.35T>G (p.Leu12Arg) rs2135819422
NM_000545.8(HNF1A):c.360G>C (p.Lys120Asn)
NM_000545.8(HNF1A):c.364T>C (p.Tyr122His) rs2135832520
NM_000545.8(HNF1A):c.365A>G (p.Tyr122Cys) rs137853237
NM_000545.8(HNF1A):c.367C>G (p.Leu123Val) rs1876669134
NM_000545.8(HNF1A):c.368T>C (p.Leu123Pro) rs2135832538
NM_000545.8(HNF1A):c.368T>G (p.Leu123Arg) rs2135832538
NM_000545.8(HNF1A):c.369GCA[4] (p.Gln125dup) rs193922596
NM_000545.8(HNF1A):c.377ACA[1] (p.Asn127del) rs2135832562
NM_000545.8(HNF1A):c.382A>G (p.Ile128Val) rs1876669657
NM_000545.8(HNF1A):c.383T>A (p.Ile128Asn) rs2135832570
NM_000545.8(HNF1A):c.385C>A (p.Pro129Thr) rs1876669818
NM_000545.8(HNF1A):c.391C>T (p.Arg131Trp) rs137853244
NM_000545.8(HNF1A):c.392G>A (p.Arg131Gln) rs753998395
NM_000545.8(HNF1A):c.392G>T (p.Arg131Leu) rs753998395
NM_000545.8(HNF1A):c.397G>A (p.Val133Met) rs2135832611
NM_000545.8(HNF1A):c.397G>T (p.Val133Leu) rs2135832611
NM_000545.8(HNF1A):c.399_405del (p.Val134fs) rs2135832615
NM_000545.8(HNF1A):c.403G>A (p.Asp135Asn) rs1876671241
NM_000545.8(HNF1A):c.404del (p.Asp135fs) rs2135832632
NM_000545.8(HNF1A):c.410C>G (p.Thr137Ser) rs1876671890
NM_000545.8(HNF1A):c.412G>A (p.Gly138Ser) rs2135832646
NM_000545.8(HNF1A):c.41C>T (p.Ala14Val) rs772214801
NM_000545.8(HNF1A):c.425C>A (p.Ser142Tyr) rs2135832668
NM_000545.8(HNF1A):c.425C>T (p.Ser142Phe) rs2135832668
NM_000545.8(HNF1A):c.427C>T (p.His143Tyr) rs2135832685
NM_000545.8(HNF1A):c.427del (p.His143fs) rs2135832675
NM_000545.8(HNF1A):c.429C>G (p.His143Gln) rs2135832689
NM_000545.8(HNF1A):c.42_51delinsTG (p.Ala15fs) rs2135819438
NM_000545.8(HNF1A):c.433T>C (p.Ser145Pro) rs1248375417
NM_000545.8(HNF1A):c.434C>T (p.Ser145Phe) rs1555211426
NM_000545.8(HNF1A):c.441C>A (p.His147Gln) rs193922597
NM_000545.8(HNF1A):c.44C>T (p.Ala15Val) rs2135819440
NM_000545.8(HNF1A):c.46C>G (p.Leu16Val) rs2135819447
NM_000545.8(HNF1A):c.475C>G (p.Arg159Gly) rs765432081
NM_000545.8(HNF1A):c.475C>T (p.Arg159Trp) rs765432081
NM_000545.8(HNF1A):c.476G>A (p.Arg159Gln) rs1172328722
NM_000545.8(HNF1A):c.47T>C (p.Leu16Pro) rs2135819448
NM_000545.8(HNF1A):c.485T>C (p.Leu162Pro) rs1555211434
NM_000545.8(HNF1A):c.490A>C (p.Thr164Pro) rs772597940
NM_000545.8(HNF1A):c.494G>A (p.Trp165Ter) rs1555211436
NM_000545.8(HNF1A):c.49C>G (p.Leu17Val) rs1876083246
NM_000545.8(HNF1A):c.4del (p.Val2fs) rs1555260207
NM_000545.8(HNF1A):c.503G>C (p.Arg168Pro)
NM_000545.8(HNF1A):c.511C>G (p.Arg171Gly) rs1057520291
NM_000545.8(HNF1A):c.511C>T (p.Arg171Ter) rs1057520291
NM_000545.8(HNF1A):c.517G>A (p.Val173Met)
NM_000545.8(HNF1A):c.518_526+37del rs386134267
NM_000545.8(HNF1A):c.526+1G>A rs1364708195
NM_000545.8(HNF1A):c.526+1G>C rs1364708195
NM_000545.8(HNF1A):c.526+1G>T
NM_000545.8(HNF1A):c.526+2dup rs1555211448
NM_000545.8(HNF1A):c.526C>T (p.Gln176Ter) rs754728827
NM_000545.8(HNF1A):c.527-1G>A rs1555211904
NM_000545.8(HNF1A):c.539C>G (p.Ala180Gly)
NM_000545.8(HNF1A):c.55T>G (p.Ser19Ala) rs1064793150
NM_000545.8(HNF1A):c.56C>T (p.Ser19Leu) rs1876084584
NM_000545.8(HNF1A):c.58G>A (p.Gly20Arg) rs1249563793
NM_000545.8(HNF1A):c.58G>C (p.Gly20Arg) rs1249563793
NM_000545.8(HNF1A):c.59G>A (p.Gly20Glu) rs1566092362
NM_000545.8(HNF1A):c.59G>C (p.Gly20Ala) rs1566092362
NM_000545.8(HNF1A):c.607C>A (p.Arg203Ser) rs1180119907
NM_000545.8(HNF1A):c.607C>T (p.Arg203Cys) rs1180119907
NM_000545.8(HNF1A):c.613A>C (p.Lys205Gln) rs2135839309
NM_000545.8(HNF1A):c.616T>A (p.Trp206Arg) rs1057524898
NM_000545.8(HNF1A):c.618G>C (p.Trp206Cys) rs2135839338
NM_000545.8(HNF1A):c.619G>T (p.Gly207Cys) rs2135839346
NM_000545.8(HNF1A):c.620G>A (p.Gly207Asp) rs1555211922
NM_000545.8(HNF1A):c.646C>T (p.Gln216Ter)
NM_000545.8(HNF1A):c.650C>G (p.Ala217Gly) rs2135839548
NM_000545.8(HNF1A):c.653A>G (p.Tyr218Cys)
NM_000545.8(HNF1A):c.663GAA[1] (p.Lys222del) rs193922599
NM_000545.8(HNF1A):c.66C>G (p.Ser22Arg)
NM_000545.8(HNF1A):c.670C>T (p.Pro224Ser) rs193922600
NM_000545.8(HNF1A):c.675del (p.Ser225fs)
NM_000545.8(HNF1A):c.676A>G (p.Lys226Glu)
NM_000545.8(HNF1A):c.676_678del (p.Lys226del) rs1555211927
NM_000545.8(HNF1A):c.682G>A (p.Glu228Lys) rs747416693
NM_000545.8(HNF1A):c.682dup (p.Glu228fs)
NM_000545.8(HNF1A):c.683A>G (p.Glu228Gly) rs2135839809
NM_000545.8(HNF1A):c.685C>G (p.Arg229Gly) rs769086289
NM_000545.8(HNF1A):c.685C>T (p.Arg229Ter) rs769086289
NM_000545.8(HNF1A):c.686G>A (p.Arg229Gln) rs1057520779
NM_000545.8(HNF1A):c.686G>C (p.Arg229Pro) rs1057520779
NM_000545.8(HNF1A):c.690_691del (p.Glu230fs)
NM_000545.8(HNF1A):c.694dup (p.Leu232fs) rs1057524908
NM_000545.8(HNF1A):c.695T>C (p.Leu232Pro)
NM_000545.8(HNF1A):c.696dup (p.Val233fs) rs2135839892
NM_000545.8(HNF1A):c.697G>C (p.Val233Leu)
NM_000545.8(HNF1A):c.697G>T (p.Val233Leu)
NM_000545.8(HNF1A):c.709A>C (p.Asn237His) rs2135839997
NM_000545.8(HNF1A):c.709A>G (p.Asn237Asp) rs2135839997
NM_000545.8(HNF1A):c.710A>C (p.Asn237Thr) rs1555211935
NM_000545.8(HNF1A):c.710A>G (p.Asn237Ser) rs1555211935
NM_000545.8(HNF1A):c.711_713del (p.Asn237_Arg238delinsLys) rs2135840027
NM_000545.8(HNF1A):c.71_72del (p.Glu24fs) rs2135819527
NM_000545.8(HNF1A):c.721T>C (p.Cys241Arg) rs2135841104
NM_000545.8(HNF1A):c.721T>G (p.Cys241Gly) rs2135841104
NM_000545.8(HNF1A):c.722G>A (p.Cys241Tyr) rs2135841113
NM_000545.8(HNF1A):c.722_725dup (p.Ile242fs) rs1555211975
NM_000545.8(HNF1A):c.725T>C (p.Ile242Thr) rs2135841137
NM_000545.8(HNF1A):c.727C>G (p.Gln243Glu)
NM_000545.8(HNF1A):c.731G>T (p.Arg244Ile) rs193922602
NM_000545.8(HNF1A):c.732A>T (p.Arg244Ser) rs2135841190
NM_000545.8(HNF1A):c.733G>A (p.Gly245Arg) rs2135841196
NM_000545.8(HNF1A):c.734G>T (p.Gly245Val) rs193922603
NM_000545.8(HNF1A):c.736G>T (p.Val246Leu) rs2135841224
NM_000545.8(HNF1A):c.737T>C (p.Val246Ala) rs2135841238
NM_000545.8(HNF1A):c.737T>G (p.Val246Gly) rs2135841238
NM_000545.8(HNF1A):c.73G>A (p.Ala25Thr) rs587778394
NM_000545.8(HNF1A):c.73G>C (p.Ala25Pro) rs587778394
NM_000545.8(HNF1A):c.745T>C (p.Ser249Pro) rs2135841315
NM_000545.8(HNF1A):c.748C>T (p.Gln250Ter) rs1308016430
NM_000545.8(HNF1A):c.749A>C (p.Gln250Pro) rs1555211982
NM_000545.8(HNF1A):c.760C>A (p.Leu254Met) rs2135841451
NM_000545.8(HNF1A):c.761T>A (p.Leu254Gln) rs2135841460
NM_000545.8(HNF1A):c.763G>A (p.Gly255Ser) rs2135841479
NM_000545.8(HNF1A):c.767C>T (p.Ser256Phe) rs1555211986
NM_000545.8(HNF1A):c.779C>A (p.Thr260Lys)
NM_000545.8(HNF1A):c.779C>G (p.Thr260Arg)
NM_000545.8(HNF1A):c.779C>T (p.Thr260Met) rs886039544
NM_000545.8(HNF1A):c.77T>C (p.Leu26Pro) rs2135819552
NM_000545.8(HNF1A):c.781G>A (p.Glu261Lys) rs2135841592
NM_000545.8(HNF1A):c.787C>T (p.Arg263Cys) rs771108132
NM_000545.8(HNF1A):c.788G>A (p.Arg263His) rs1057520504
NM_000545.8(HNF1A):c.788G>T (p.Arg263Leu) rs1057520504
NM_000545.8(HNF1A):c.790G>T (p.Val264Phe) rs193922604
NM_000545.8(HNF1A):c.790_791del (p.Val264fs) rs1555211999
NM_000545.8(HNF1A):c.794A>C (p.Tyr265Ser) rs1555212006
NM_000545.8(HNF1A):c.794A>G (p.Tyr265Cys) rs1555212006
NM_000545.8(HNF1A):c.797A>G (p.Asn266Ser) rs2135841726
NM_000545.8(HNF1A):c.798C>G (p.Asn266Lys) rs2135841730
NM_000545.8(HNF1A):c.801_802insGGG (p.Trp267_Phe268insGly) rs1555212009
NM_000545.8(HNF1A):c.802T>A (p.Phe268Ile) rs2135841769
NM_000545.8(HNF1A):c.802T>C (p.Phe268Leu) rs2135841769
NM_000545.8(HNF1A):c.803T>C (p.Phe268Ser) rs193922605
NM_000545.8(HNF1A):c.80T>C (p.Ile27Thr) rs2135819576
NM_000545.8(HNF1A):c.80T>G (p.Ile27Ser) rs2135819576
NM_000545.8(HNF1A):c.811C>G (p.Arg271Gly) rs886039386
NM_000545.8(HNF1A):c.811C>T (p.Arg271Trp) rs886039386
NM_000545.8(HNF1A):c.811del (p.Arg271fs) rs2135841855
NM_000545.8(HNF1A):c.814C>A (p.Arg272Ser) rs1555212014
NM_000545.8(HNF1A):c.814C>T (p.Arg272Cys) rs1555212014
NM_000545.8(HNF1A):c.815G>A (p.Arg272His) rs137853238
NM_000545.8(HNF1A):c.817A>C (p.Lys273Gln) rs1555212016
NM_000545.8(HNF1A):c.827C>A (p.Ala276Asp) rs137853245
NM_000545.8(HNF1A):c.82C>T (p.Gln28Ter) rs2135819583
NM_000545.8(HNF1A):c.85G>C (p.Ala29Pro) rs1876087643
NM_000545.8(HNF1A):c.864del (p.Pro291fs) rs762703502
NM_000545.8(HNF1A):c.864dup (p.Pro289fs) rs762703502
NM_000545.8(HNF1A):c.865C>T (p.Pro289Ser) rs765829022
NM_000545.8(HNF1A):c.866C>A (p.Pro289His) rs267603343
NM_000545.8(HNF1A):c.866C>G (p.Pro289Arg) rs267603343
NM_000545.8(HNF1A):c.870C>T (p.Pro290=) rs779008957
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.872C>T (p.Pro291Leu) rs193922606
NM_000545.8(HNF1A):c.872del (p.Pro291fs) rs587776825
NM_000545.8(HNF1A):c.872dup (p.Gly292fs) rs587776825
NM_000545.8(HNF1A):c.94G>T (p.Glu32Ter) rs1388926124
NM_000545.8(HNF1A):c.956-1G>A rs1565886545
NM_000545.8(HNF1A):c.956-1G>C rs1565886545
NM_000545.8(HNF1A):c.956-1G>T rs1565886545
NM_000545.8(HNF1A):c.956-2A>G
NM_000545.8(HNF1A):c.98C>G (p.Pro33Arg) rs1001854457
NM_000545.8(HNF1A):c.98C>T (p.Pro33Leu) rs1001854457
Single allele rs2135818764

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