ClinVar Miner

List of variants in gene HNF1B reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 113
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HGVS dbSNP gnomAD frequency
NM_000458.4(HNF1B):c.1535-188C>T rs75148877 0.01577
NM_000458.4(HNF1B):c.1340-303T>A rs112298654 0.01150
NM_000458.4(HNF1B):c.1207-66G>A rs114224174 0.00644
NM_000458.4(HNF1B):c.1535-44G>C rs10083829 0.00552
NM_000458.3(HNF1B):c.-178G>A rs148442901 0.00528
NM_000458.4(HNF1B):c.1207-54G>A rs138615516 0.00456
NM_000458.4(HNF1B):c.344+196C>A rs376100923 0.00391
NM_000458.4(HNF1B):c.810-32T>C rs752563696 0.00384
NM_000458.4(HNF1B):c.344+198T>G rs373107533 0.00344
NM_000458.4(HNF1B):c.1413C>T (p.Pro471=) rs140781855 0.00325
NM_000458.4(HNF1B):c.444G>A (p.Ser148=) rs147218489 0.00228
NM_000458.4(HNF1B):c.1207-18T>C rs199849203 0.00026
NM_000458.4(HNF1B):c.1594A>G (p.Met532Val) rs141193981 0.00022
NM_000458.4(HNF1B):c.852C>T (p.His284=) rs149581999 0.00022
NM_000458.4(HNF1B):c.1668C>A (p.Ala556=) rs144354798 0.00019
NM_000458.4(HNF1B):c.1046-12G>A rs201751705 0.00014
NM_000458.4(HNF1B):c.420C>T (p.Val140=) rs370134885 0.00011
NM_000458.4(HNF1B):c.1534+11G>A rs373875820 0.00009
NM_000458.4(HNF1B):c.1578C>G (p.Ser526=) rs751225159 0.00009
NM_000458.4(HNF1B):c.1637T>C (p.Met546Thr) rs551889844 0.00009
NM_000458.4(HNF1B):c.1654-9T>A rs200579660 0.00009
NM_000458.4(HNF1B):c.*22G>A rs200421746 0.00007
NM_000458.4(HNF1B):c.1534+10C>T rs368168569 0.00007
NM_000458.4(HNF1B):c.1339+17G>A rs374854968 0.00006
NM_000458.4(HNF1B):c.313G>A (p.Glu105Lys) rs199572129 0.00006
NM_000458.4(HNF1B):c.36C>T (p.Leu12=) rs749370057 0.00006
NM_000458.4(HNF1B):c.948C>T (p.Asp316=) rs373132003 0.00006
NM_000458.4(HNF1B):c.1239C>T (p.Val413=) rs201113814 0.00005
NM_000458.4(HNF1B):c.1654-4G>A rs193922485 0.00005
NM_000458.4(HNF1B):c.1008C>T (p.His336=) rs150268130 0.00004
NM_000458.4(HNF1B):c.1539C>T (p.Tyr513=) rs780554506 0.00004
NM_000458.4(HNF1B):c.100C>T (p.Leu34=) rs373201245 0.00003
NM_000458.4(HNF1B):c.9C>T (p.Ser3=) rs773256244 0.00003
NM_000458.4(HNF1B):c.1207-5A>G rs368068840 0.00001
NM_000458.4(HNF1B):c.1434G>A (p.Leu478=) rs574876963 0.00001
NM_000458.4(HNF1B):c.231C>G (p.Asp77Glu) rs760448993 0.00001
NM_000458.4(HNF1B):c.66C>A (p.Thr22=) rs906719754 0.00001
NM_000458.4(HNF1B):c.-27A>C rs1402766102
NM_000458.4(HNF1B):c.1005C>T (p.Pro335=)
NM_000458.4(HNF1B):c.1006C>G (p.His336Asp)
NM_000458.4(HNF1B):c.1011C>T (p.His337=)
NM_000458.4(HNF1B):c.102G>T (p.Leu34=)
NM_000458.4(HNF1B):c.1046-11T>G
NM_000458.4(HNF1B):c.107C>T (p.Ser36Phe)
NM_000458.4(HNF1B):c.1080C>T (p.Ile360=)
NM_000458.4(HNF1B):c.1108G>A (p.Gly370Ser)
NM_000458.4(HNF1B):c.1152C>A (p.Val384=)
NM_000458.4(HNF1B):c.1188C>T (p.Leu396=)
NM_000458.4(HNF1B):c.1206+16C>T
NM_000458.4(HNF1B):c.1207-15T>C
NM_000458.4(HNF1B):c.1207-7C>T rs1215174368
NM_000458.4(HNF1B):c.1239C>G (p.Val413=)
NM_000458.4(HNF1B):c.1266C>A (p.Leu422=)
NM_000458.4(HNF1B):c.1278T>C (p.Asn426=)
NM_000458.4(HNF1B):c.127C>T (p.Leu43=)
NM_000458.4(HNF1B):c.1383T>C (p.Ser461=)
NM_000458.4(HNF1B):c.1389C>T (p.Ala463=) rs761684626
NM_000458.4(HNF1B):c.1396C>T (p.Leu466=)
NM_000458.4(HNF1B):c.1455C>T (p.Pro485=)
NM_000458.4(HNF1B):c.1474G>A (p.Gly492Ser)
NM_000458.4(HNF1B):c.1534+16T>C
NM_000458.4(HNF1B):c.1535-12C>T
NM_000458.4(HNF1B):c.1535-12_1535-11del
NM_000458.4(HNF1B):c.1535-15A>T
NM_000458.4(HNF1B):c.1535-17T>C
NM_000458.4(HNF1B):c.1535-6C>T rs1373821018
NM_000458.4(HNF1B):c.1608T>C (p.Asp536=)
NM_000458.4(HNF1B):c.1629C>T (p.Leu543=)
NM_000458.4(HNF1B):c.162C>A (p.Ala54=)
NM_000458.4(HNF1B):c.1653+20C>T
NM_000458.4(HNF1B):c.1654-11T>C rs193922484
NM_000458.4(HNF1B):c.1654-14CT[4] rs886052890
NM_000458.4(HNF1B):c.1654-14CT[6]
NM_000458.4(HNF1B):c.1654-14_1654-10del
NM_000458.4(HNF1B):c.1654-16T>A
NM_000458.4(HNF1B):c.168C>T (p.Pro56=)
NM_000458.4(HNF1B):c.182T>G (p.Val61Gly)
NM_000458.4(HNF1B):c.195C>T (p.Leu65=)
NM_000458.4(HNF1B):c.226G>T (p.Gly76Cys)
NM_000458.4(HNF1B):c.237C>T (p.Gly79=)
NM_000458.4(HNF1B):c.240C>G (p.Ser80=)
NM_000458.4(HNF1B):c.244G>A (p.Asp82Asn)
NM_000458.4(HNF1B):c.246C>T (p.Asp82=)
NM_000458.4(HNF1B):c.249C>G (p.Gly83=)
NM_000458.4(HNF1B):c.270C>T (p.Pro90=)
NM_000458.4(HNF1B):c.288G>A (p.Gln96=)
NM_000458.4(HNF1B):c.321G>T (p.Arg107=)
NM_000458.4(HNF1B):c.345-4C>T rs200590728
NM_000458.4(HNF1B):c.345-8C>G
NM_000458.4(HNF1B):c.354T>C (p.Pro118=)
NM_000458.4(HNF1B):c.375C>A (p.Ile125=)
NM_000458.4(HNF1B):c.429C>T (p.Thr143=)
NM_000458.4(HNF1B):c.450C>T (p.Leu150=)
NM_000458.4(HNF1B):c.486C>A (p.Thr162=)
NM_000458.4(HNF1B):c.498C>T (p.Ala166=)
NM_000458.4(HNF1B):c.507C>T (p.Tyr169=)
NM_000458.4(HNF1B):c.516C>T (p.Tyr172=) rs764561297
NM_000458.4(HNF1B):c.544+14T>C
NM_000458.4(HNF1B):c.544+15C>G
NM_000458.4(HNF1B):c.60G>A (p.Gly20=)
NM_000458.4(HNF1B):c.76C>T (p.Leu26=)
NM_000458.4(HNF1B):c.810-14C>T
NM_000458.4(HNF1B):c.810-18C>T
NM_000458.4(HNF1B):c.810-19C>T
NM_000458.4(HNF1B):c.831G>A (p.Gly277=) rs199797518
NM_000458.4(HNF1B):c.855C>T (p.Gly285=)
NM_000458.4(HNF1B):c.879G>A (p.Glu293=)
NM_000458.4(HNF1B):c.933A>G (p.Gln311=)
NM_000458.4(HNF1B):c.972C>T (p.His324=) rs753631084
NM_000458.4(HNF1B):c.987G>A (p.Leu329=) rs2147544778
NM_000458.4(HNF1B):c.996C>T (p.His332=)
NM_000458.4(HNF1B):c.999C>T (p.Gly333=)
NM_000458.4(HNF1B):c.9C>G (p.Ser3=)

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