ClinVar Miner

List of variants in gene HNF1A reported as likely benign by Invitae

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Gene type:
ClinVar version:
Total variants: 141
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HGVS dbSNP gnomAD frequency
NM_000545.8(HNF1A):c.155G>C (p.Gly52Ala) rs142318174 0.00083
NM_000545.8(HNF1A):c.92G>A (p.Gly31Asp) rs137853247 0.00076
NM_000545.8(HNF1A):c.1748G>A (p.Arg583Gln) rs137853242 0.00060
NM_000545.8(HNF1A):c.965A>G (p.Tyr322Cys) rs140491072 0.00041
NM_000545.8(HNF1A):c.1501+6C>T rs374306837 0.00035
NM_000545.8(HNF1A):c.1386C>T (p.Val462=) rs143015301 0.00021
NM_000545.8(HNF1A):c.1108-4G>A rs372892932 0.00020
NM_000545.8(HNF1A):c.1756G>A (p.Ala586Thr) rs373857078 0.00017
NM_000545.8(HNF1A):c.693G>A (p.Thr231=) rs145240086 0.00017
NM_000545.8(HNF1A):c.716C>T (p.Ala239Val) rs587778397 0.00016
NM_000545.8(HNF1A):c.521C>T (p.Ala174Val) rs201934320 0.00013
NM_000545.8(HNF1A):c.1272T>C (p.Pro424=) rs141324437 0.00011
NM_000545.8(HNF1A):c.225C>T (p.Asp75=) rs202180554 0.00009
NM_000545.8(HNF1A):c.1593C>T (p.Ser531=) rs370300688 0.00008
NM_000545.8(HNF1A):c.1674G>A (p.Pro558=) rs780280661 0.00007
NM_000545.8(HNF1A):c.42G>A (p.Ala14=) rs775391034 0.00007
NM_000545.8(HNF1A):c.542G>C (p.Gly181Ala) rs773315874 0.00007
NM_000545.8(HNF1A):c.1011C>T (p.Ser337=) rs549471872 0.00006
NM_000545.8(HNF1A):c.1071G>A (p.Glu357=) rs376279459 0.00006
NM_000545.8(HNF1A):c.1729C>G (p.His577Asp) rs376832928 0.00006
NM_000545.8(HNF1A):c.954C>T (p.His318=) rs193922607 0.00006
NM_000545.8(HNF1A):c.99G>A (p.Pro33=) rs538619966 0.00006
NM_000545.8(HNF1A):c.480C>T (p.Ala160=) rs368536974 0.00005
NM_000545.8(HNF1A):c.1015G>A (p.Gly339Ser) rs766790596 0.00004
NM_000545.8(HNF1A):c.1502-14T>C rs765596650 0.00004
NM_000545.8(HNF1A):c.150C>T (p.Cys50=) rs193922583 0.00004
NM_000545.8(HNF1A):c.527-18G>A rs375259151 0.00004
NM_000545.8(HNF1A):c.713+13G>A rs755961371 0.00004
NM_000545.8(HNF1A):c.713+8G>A rs1202882892 0.00004
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.216C>T (p.Asp72=) rs148961412 0.00002
NM_000545.8(HNF1A):c.978G>A (p.Ala326=) rs200351196 0.00002
NM_000545.8(HNF1A):c.1108-15G>A rs1395103510 0.00001
NM_000545.8(HNF1A):c.1108-6del rs1439874755 0.00001
NM_000545.8(HNF1A):c.1170G>A (p.Glu390=) rs761882013 0.00001
NM_000545.8(HNF1A):c.1281C>T (p.Thr427=) rs1345001140 0.00001
NM_000545.8(HNF1A):c.1521C>A (p.Pro507=) rs977750039 0.00001
NM_000545.8(HNF1A):c.153C>T (p.Gly51=) rs761779651 0.00001
NM_000545.8(HNF1A):c.1623+20G>A rs1012229716 0.00001
NM_000545.8(HNF1A):c.246G>A (p.Thr82=) rs752243228 0.00001
NM_000545.8(HNF1A):c.326+18G>A rs1166992434 0.00001
NM_000545.8(HNF1A):c.537T>C (p.His179=) rs765329757 0.00001
NM_000545.8(HNF1A):c.681G>A (p.Glu227=) rs780613374 0.00001
NM_000545.8(HNF1A):c.685C>A (p.Arg229=) rs769086289 0.00001
NM_000545.8(HNF1A):c.713+14C>T rs193922601 0.00001
NM_000545.8(HNF1A):c.759G>T (p.Gly253=) rs749946974 0.00001
NM_000545.8(HNF1A):c.780G>A (p.Thr260=) rs749633685 0.00001
NM_000545.8(HNF1A):c.867C>G (p.Pro289=) rs907312892 0.00001
NM_000545.8(HNF1A):c.894G>A (p.Ala298=) rs951696015 0.00001
NM_000545.8(HNF1A):c.-123G>A
NM_000545.8(HNF1A):c.-124G>C rs563304627
NM_000545.8(HNF1A):c.1014C>T (p.Gly338=)
NM_000545.8(HNF1A):c.1062G>T (p.Thr354=)
NM_000545.8(HNF1A):c.1107+14C>T
NM_000545.8(HNF1A):c.1107+15T>C
NM_000545.8(HNF1A):c.1107+17G>C
NM_000545.8(HNF1A):c.1113A>G (p.Ser371=)
NM_000545.8(HNF1A):c.1230G>A (p.Gly410=)
NM_000545.8(HNF1A):c.1242C>T (p.Ile414=)
NM_000545.8(HNF1A):c.126C>G (p.Gly42=)
NM_000545.8(HNF1A):c.126C>T (p.Gly42=)
NM_000545.8(HNF1A):c.1275G>A (p.Thr425=)
NM_000545.8(HNF1A):c.1309+19G>A
NM_000545.8(HNF1A):c.1309+20T>G
NM_000545.8(HNF1A):c.1310-8C>T rs913705079
NM_000545.8(HNF1A):c.132G>A (p.Leu44=)
NM_000545.8(HNF1A):c.1341G>A (p.Pro447=)
NM_000545.8(HNF1A):c.1383C>A (p.Pro461=) rs772756175
NM_000545.8(HNF1A):c.1395C>T (p.Ser465=)
NM_000545.8(HNF1A):c.13C>T (p.Leu5=)
NM_000545.8(HNF1A):c.1401G>A (p.Pro467=)
NM_000545.8(HNF1A):c.1424C>T (p.Pro475Leu) rs193922580
NM_000545.8(HNF1A):c.1455C>G (p.Thr485=)
NM_000545.8(HNF1A):c.1455C>T (p.Thr485=)
NM_000545.8(HNF1A):c.1464C>G (p.Pro488=) rs765827203
NM_000545.8(HNF1A):c.1464C>T (p.Pro488=)
NM_000545.8(HNF1A):c.1486C>T (p.Leu496=)
NM_000545.8(HNF1A):c.1497C>A (p.Pro499=)
NM_000545.8(HNF1A):c.1501+15C>T
NM_000545.8(HNF1A):c.1501+16C>T
NM_000545.8(HNF1A):c.1501+7G>C rs2464195
NM_000545.8(HNF1A):c.1502-8G>T
NM_000545.8(HNF1A):c.155_156delinsCT (p.Gly52Ala) rs587778393
NM_000545.8(HNF1A):c.1560G>A (p.Gln520=) rs1877296271
NM_000545.8(HNF1A):c.1569C>A (p.Leu523=)
NM_000545.8(HNF1A):c.1569C>T (p.Leu523=)
NM_000545.8(HNF1A):c.1575C>T (p.Thr525=)
NM_000545.8(HNF1A):c.1584C>T (p.Thr528=)
NM_000545.8(HNF1A):c.1602C>T (p.Ala534=)
NM_000545.8(HNF1A):c.1623+11G>A
NM_000545.8(HNF1A):c.1624-6C>T
NM_000545.8(HNF1A):c.1624-7C>T
NM_000545.8(HNF1A):c.1638C>T (p.Asp546=)
NM_000545.8(HNF1A):c.1680T>G (p.Ser560=)
NM_000545.8(HNF1A):c.1698C>T (p.His566=)
NM_000545.8(HNF1A):c.1713C>T (p.Asp571=)
NM_000545.8(HNF1A):c.1719_1720inv (p.Ser574Gly)
NM_000545.8(HNF1A):c.1740G>A (p.Pro580=)
NM_000545.8(HNF1A):c.1743C>G (p.Ala581=)
NM_000545.8(HNF1A):c.1743C>T (p.Ala581=)
NM_000545.8(HNF1A):c.1747C>A (p.Arg583=)
NM_000545.8(HNF1A):c.1768+20C>G
NM_000545.8(HNF1A):c.204G>A (p.Arg68=)
NM_000545.8(HNF1A):c.222G>A (p.Thr74=)
NM_000545.8(HNF1A):c.261A>G (p.Lys87=)
NM_000545.8(HNF1A):c.306C>T (p.Ala102=) rs1486966222
NM_000545.8(HNF1A):c.326+17C>T
NM_000545.8(HNF1A):c.327-18G>A
NM_000545.8(HNF1A):c.327-19C>T
NM_000545.8(HNF1A):c.348G>A (p.Ala116=)
NM_000545.8(HNF1A):c.417C>T (p.Leu139=)
NM_000545.8(HNF1A):c.420C>T (p.Asn140=)
NM_000545.8(HNF1A):c.498C>T (p.Tyr166=) rs1876675633
NM_000545.8(HNF1A):c.522G>A (p.Ala174=)
NM_000545.8(HNF1A):c.526+13C>T
NM_000545.8(HNF1A):c.588C>G (p.Thr196=)
NM_000545.8(HNF1A):c.63G>T (p.Leu21=)
NM_000545.8(HNF1A):c.693G>T (p.Thr231=)
NM_000545.8(HNF1A):c.705G>A (p.Glu235=)
NM_000545.8(HNF1A):c.708C>T (p.Cys236=)
NM_000545.8(HNF1A):c.713+10C>T
NM_000545.8(HNF1A):c.713+11G>A
NM_000545.8(HNF1A):c.713+15G>A
NM_000545.8(HNF1A):c.713+7C>T
NM_000545.8(HNF1A):c.713+9G>T
NM_000545.8(HNF1A):c.750G>A (p.Gln250=)
NM_000545.8(HNF1A):c.765C>G (p.Gly255=) rs757910486
NM_000545.8(HNF1A):c.841C>T (p.Leu281=)
NM_000545.8(HNF1A):c.852C>T (p.Asp284=)
NM_000545.8(HNF1A):c.855G>A (p.Thr285=)
NM_000545.8(HNF1A):c.861C>T (p.Ser287=)
NM_000545.8(HNF1A):c.870C>A (p.Pro290=) rs779008957
NM_000545.8(HNF1A):c.870C>G (p.Pro290=)
NM_000545.8(HNF1A):c.870C>T (p.Pro290=) rs779008957
NM_000545.8(HNF1A):c.879A>T (p.Pro293=)
NM_000545.8(HNF1A):c.87A>G (p.Ala29=)
NM_000545.8(HNF1A):c.885G>A (p.Pro295=)
NM_000545.8(HNF1A):c.956-4C>T
NM_000545.8(HNF1A):c.956-8C>T rs762339992
NM_000545.8(HNF1A):c.969A>G (p.Gly323=)

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