Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.37731598_37731833delCA913190764HNF1Bc.811_1045+1del
c.733_967+1del
n.263_498del
 ClinVar ClinVar
17g.37731599_37733825delCA915950000HNF1Bc.545_1045del
c.545-78_967del
17g.37731601G>ACA499602428HNF1Bc.1039C>T (p.Leu347=)
c.961C>T (p.Leu321=)
n.491C>T
17g.37731601G>CCA398745861HNF1Bc.1039C>G (p.Leu347Val)
c.961C>G (p.Leu321Val)
n.491C>G
17g.37731601G>TCA398745863HNF1Bc.1039C>A (p.Leu347Met)
c.961C>A (p.Leu321Met)
n.491C>A
17g.37731602C>ACA398745881HNF1Bc.1038G>T (p.Lys346Asn)
c.960G>T (p.Lys320Asn)
n.490G>T
17g.37731602C>GCA398745886HNF1Bc.1038G>C (p.Lys346Asn)
c.960G>C (p.Lys320Asn)
n.490G>C
17g.37731602C>TCA499602429HNF1Bc.1038G>A (p.Lys346=)
c.960G>A (p.Lys320=)
n.490G>A
 gnomAD v4
17g.37731603T>ACA398745893HNF1Bc.1037A>T (p.Lys346Met)
c.959A>T (p.Lys320Met)
n.489A>T
17g.37731603T>CCA398745894HNF1Bc.1037A>G (p.Lys346Arg)
c.959A>G (p.Lys320Arg)
n.489A>G
17g.37731603T>GCA398745892HNF1Bc.1037A>C (p.Lys346Thr)
c.959A>C (p.Lys320Thr)
n.489A>C
17g.37731604T>ACA398745896HNF1Bc.1036A>T (p.Lys346Ter)
c.958A>T (p.Lys320Ter)
n.488A>T
17g.37731604T>CCA398745900HNF1Bc.1036A>G (p.Lys346Glu)
c.958A>G (p.Lys320Glu)
n.488A>G
 gnomAD v4
17g.37731604T>GCA398745904HNF1Bc.1036A>C (p.Lys346Gln)
c.958A>C (p.Lys320Gln)
n.488A>C
17g.37731605G>ACA499602433HNF1Bc.1035C>T (p.Asn345=)
c.957C>T (p.Asn319=)
n.487C>T
 gnomAD v4
17g.37731605G>CCA398745907HNF1Bc.1035C>G (p.Asn345Lys)
c.957C>G (p.Asn319Lys)
n.487C>G
17g.37731605G>TCA398745908HNF1Bc.1035C>A (p.Asn345Lys)
c.957C>A (p.Asn319Lys)
n.487C>A
17g.37731606T>ACA398745909HNF1Bc.1034A>T (p.Asn345Ile)
c.956A>T (p.Asn319Ile)
n.486A>T
17g.37731606T>CCA398745910HNF1Bc.1034A>G (p.Asn345Ser)
c.956A>G (p.Asn319Ser)
n.486A>G
17g.37731606T>GCA398745914HNF1Bc.1034A>C (p.Asn345Thr)
c.956A>C (p.Asn319Thr)
n.486A>C
17g.37731607T>ACA398745920HNF1Bc.1033A>T (p.Asn345Tyr)
c.955A>T (p.Asn319Tyr)
n.485A>T
17g.37731607T>CCA8518946HNF1Bc.1033A>G (p.Asn345Asp)
c.955A>G (p.Asn319Asp)
n.485A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37731607T>GCA398745925HNF1Bc.1033A>C (p.Asn345His)
c.955A>C (p.Asn319His)
n.485A>C
17g.37731608T>ACA499602435HNF1Bc.1032A>T (p.Pro344=)
c.954A>T (p.Pro318=)
n.484A>T
 dbSNP gnomAD v3 gnomAD v4
17g.37731608T>CCA499602436HNF1Bc.1032A>G (p.Pro344=)
c.954A>G (p.Pro318=)
n.484A>G
17g.37731608T>GCA499602437HNF1Bc.1032A>C (p.Pro344=)
c.954A>C (p.Pro318=)
n.484A>C
17g.37731609G>ACA398745942HNF1Bc.1031C>T (p.Pro344Leu)
c.953C>T (p.Pro318Leu)
n.483C>T
17g.37731609G>CCA398745935HNF1Bc.1031C>G (p.Pro344Arg)
c.953C>G (p.Pro318Arg)
n.483C>G
17g.37731609G>TCA398745930HNF1Bc.1031C>A (p.Pro344Gln)
c.953C>A (p.Pro318Gln)
n.483C>A
 gnomAD v4
17g.37731610G>ACA398745945HNF1Bc.1030C>T (p.Pro344Ser)
c.952C>T (p.Pro318Ser)
n.482C>T
17g.37731610G>CCA398745951HNF1Bc.1030C>G (p.Pro344Ala)
c.952C>G (p.Pro318Ala)
n.482C>G
17g.37731610G>TCA398745956HNF1Bc.1030C>A (p.Pro344Thr)
c.952C>A (p.Pro318Thr)
n.482C>A
 gnomAD v4
17g.37731611A>CCA499602439HNF1Bc.1029T>G (p.Pro343=)
c.951T>G (p.Pro317=)
n.481T>G
17g.37731611A>GCA499602440HNF1Bc.1029T>C (p.Pro343=)
c.951T>C (p.Pro317=)
n.481T>C
17g.37731611A>TCA499602441HNF1Bc.1029T>A (p.Pro343=)
c.951T>A (p.Pro317=)
n.481T>A
17g.37731612G>ACA398745959HNF1Bc.1028C>T (p.Pro343Leu)
c.950C>T (p.Pro317Leu)
n.480C>T
 dbSNP
17g.37731612G>CCA398745960HNF1Bc.1028C>G (p.Pro343Arg)
c.950C>G (p.Pro317Arg)
n.480C>G
17g.37731612G>TCA398745963HNF1Bc.1028C>A (p.Pro343His)
c.950C>A (p.Pro317His)
n.480C>A
17g.37731613G>ACA398745967HNF1Bc.1027C>T (p.Pro343Ser)
c.949C>T (p.Pro317Ser)
n.479C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.37731613G>CCA398745972HNF1Bc.1027C>G (p.Pro343Ala)
c.949C>G (p.Pro317Ala)
n.479C>G
17g.37731613G>TCA398745976HNF1Bc.1027C>A (p.Pro343Thr)
c.949C>A (p.Pro317Thr)
n.479C>A
17g.37731614A>CCA499602442HNF1Bc.1026T>G (p.Ser342=)
c.948T>G (p.Ser316=)
n.478T>G
17g.37731614A>GCA499602443HNF1Bc.1026T>C (p.Ser342=)
c.948T>C (p.Ser316=)
n.478T>C
17g.37731614A>TCA499602444HNF1Bc.1026T>A (p.Ser342=)
c.948T>A (p.Ser316=)
n.478T>A
17g.37731615G>ACA8518947HNF1Bc.1025C>T (p.Ser342Phe)
c.947C>T (p.Ser316Phe)
n.477C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37731615G>CCA398745978HNF1Bc.1025C>G (p.Ser342Cys)
c.947C>G (p.Ser316Cys)
n.477C>G
 gnomAD v4
17g.37731615G>TCA398745979HNF1Bc.1025C>A (p.Ser342Tyr)
c.947C>A (p.Ser316Tyr)
n.477C>A
17g.37731616A>CCA398745983HNF1Bc.1024T>G (p.Ser342Ala)
c.946T>G (p.Ser316Ala)
n.476T>G
17g.37731616A>GCA398745993HNF1Bc.1024T>C (p.Ser342Pro)
c.946T>C (p.Ser316Pro)
n.476T>C
 ClinVar dbSNP gnomAD v2 gnomAD v4
17g.37731616A>TCA398745980HNF1Bc.1024T>A (p.Ser342Thr)
c.946T>A (p.Ser316Thr)
n.476T>A
17g.37731617G>ACA499602450HNF1Bc.1023C>T (p.Ser341=)
c.945C>T (p.Ser315=)
n.475C>T
 dbSNP gnomAD v2 gnomAD v4
17g.37731617G>CCA499602448HNF1Bc.1023C>G (p.Ser341=)
c.945C>G (p.Ser315=)
n.475C>G
17g.37731617G>TCA499602449HNF1Bc.1023C>A (p.Ser341=)
c.945C>A (p.Ser315=)
n.475C>A
17g.37731618G>ACA398745997HNF1Bc.1022C>T (p.Ser341Phe)
c.944C>T (p.Ser315Phe)
n.474C>T
 gnomAD v4
17g.37731618G>CCA398746005HNF1Bc.1022C>G (p.Ser341Cys)
c.944C>G (p.Ser315Cys)
n.474C>G
17g.37731618G>TCA398746014HNF1Bc.1022C>A (p.Ser341Tyr)
c.944C>A (p.Ser315Tyr)
n.474C>A
17g.37731619A>CCA398746019HNF1Bc.1021T>G (p.Ser341Ala)
c.943T>G (p.Ser315Ala)
n.473T>G
17g.37731619A>GCA398746026HNF1Bc.1021T>C (p.Ser341Pro)
c.943T>C (p.Ser315Pro)
n.473T>C
17g.37731619A>TCA398746029HNF1Bc.1021T>A (p.Ser341Thr)
c.943T>A (p.Ser315Thr)
n.473T>A
17g.37731620G>ACA499602452HNF1Bc.1020C>T (p.Ser340=)
c.942C>T (p.Ser314=)
n.472C>T
17g.37731620G>CCA398746043HNF1Bc.1020C>G (p.Ser340Arg)
c.942C>G (p.Ser314Arg)
n.472C>G
17g.37731620G>TCA398746038HNF1Bc.1020C>A (p.Ser340Arg)
c.942C>A (p.Ser314Arg)
n.472C>A
17g.37731621C>ACA398746047HNF1Bc.1019G>T (p.Ser340Ile)
c.941G>T (p.Ser314Ile)
n.471G>T
17g.37731621C>GCA398746049HNF1Bc.1019G>C (p.Ser340Thr)
c.941G>C (p.Ser314Thr)
n.471G>C
17g.37731621C>TCA398746052HNF1Bc.1019G>A (p.Ser340Asn)
c.941G>A (p.Ser314Asn)
n.471G>A
 gnomAD v4
17g.37731622T>ACA398746056HNF1Bc.1018A>T (p.Ser340Cys)
c.940A>T (p.Ser314Cys)
n.470A>T
17g.37731622T>CCA398746069HNF1Bc.1018A>G (p.Ser340Gly)
c.940A>G (p.Ser314Gly)
n.470A>G
17g.37731622T>GCA398746072HNF1Bc.1018A>C (p.Ser340Arg)
c.940A>C (p.Ser314Arg)
n.470A>C
17g.37731623G>ACA499602454HNF1Bc.1017C>T (p.Pro339=)
c.939C>T (p.Pro313=)
n.469C>T
 dbSNP
17g.37731623G>CCA499602455HNF1Bc.1017C>G (p.Pro339=)
c.939C>G (p.Pro313=)
n.469C>G
17g.37731623G>TCA499602456HNF1Bc.1017C>A (p.Pro339=)
c.939C>A (p.Pro313=)
n.469C>A
17g.37731624G>ACA398746083HNF1Bc.1016C>T (p.Pro339Leu)
c.938C>T (p.Pro313Leu)
n.468C>T
 gnomAD v4
17g.37731624G>CCA398746076HNF1Bc.1016C>G (p.Pro339Arg)
c.938C>G (p.Pro313Arg)
n.468C>G
 dbSNP gnomAD v2 gnomAD v4
17g.37731624G>TCA398746078HNF1Bc.1016C>A (p.Pro339His)
c.938C>A (p.Pro313His)
n.468C>A
17g.37731625G>ACA398746087HNF1Bc.1015C>T (p.Pro339Ser)
c.937C>T (p.Pro313Ser)
n.467C>T
17g.37731625G>CCA398746090HNF1Bc.1015C>G (p.Pro339Ala)
c.937C>G (p.Pro313Ala)
n.467C>G
17g.37731625G>TCA398746093HNF1Bc.1015C>A (p.Pro339Thr)
c.937C>A (p.Pro313Thr)
n.467C>A
17g.37731626C>ACA398746096HNF1Bc.1014G>T (p.Gln338His)
c.936G>T (p.Gln312His)
n.466G>T
17g.37731626C>GCA398746101HNF1Bc.1014G>C (p.Gln338His)
c.936G>C (p.Gln312His)
n.466G>C
17g.37731626C>TCA499602462HNF1Bc.1014G>A (p.Gln338=)
c.936G>A (p.Gln312=)
n.466G>A
 gnomAD v4
17g.37731627T>ACA398746104HNF1Bc.1013A>T (p.Gln338Leu)
c.935A>T (p.Gln312Leu)
n.465A>T
17g.37731627T>CCA398746105HNF1Bc.1013A>G (p.Gln338Arg)
c.935A>G (p.Gln312Arg)
n.465A>G
17g.37731627T>GCA398746106HNF1Bc.1013A>C (p.Gln338Pro)
c.935A>C (p.Gln312Pro)
n.465A>C
17g.37731633_37731635delCA625879250HNF1Bc.1011_1013del (p.His337del)
c.933_935del (p.His311del)
n.463_465del
 dbSNP gnomAD v2 gnomAD v4
17g.37731628G>ACA398746107HNF1Bc.1012C>T (p.Gln338Ter)
c.934C>T (p.Gln312Ter)
n.464C>T
17g.37731628G>CCA398746110HNF1Bc.1012C>G (p.Gln338Glu)
c.934C>G (p.Gln312Glu)
n.464C>G
17g.37731628G>TCA398746111HNF1Bc.1012C>A (p.Gln338Lys)
c.934C>A (p.Gln312Lys)
n.464C>A
 dbSNP gnomAD v2 gnomAD v4
17g.37731629G>ACA499602465HNF1Bc.1011C>T (p.His337=)
c.933C>T (p.His311=)
n.463C>T
 ClinVar dbSNP gnomAD v4
17g.37731629G>CCA398746114HNF1Bc.1011C>G (p.His337Gln)
c.933C>G (p.His311Gln)
n.463C>G
 gnomAD v4
17g.37731629G>TCA398746116HNF1Bc.1011C>A (p.His337Gln)
c.933C>A (p.His311Gln)
n.463C>A
17g.37731630T>ACA398746118HNF1Bc.1010A>T (p.His337Leu)
c.932A>T (p.His311Leu)
n.462A>T
17g.37731630T>CCA398746125HNF1Bc.1010A>G (p.His337Arg)
c.932A>G (p.His311Arg)
n.462A>G
17g.37731630T>GCA398746120HNF1Bc.1010A>C (p.His337Pro)
c.932A>C (p.His311Pro)
n.462A>C
17g.37731631G>ACA398746135HNF1Bc.1009C>T (p.His337Tyr)
c.931C>T (p.His311Tyr)
n.461C>T
17g.37731631G>CCA8518948HNF1Bc.1009C>G (p.His337Asp)
c.931C>G (p.His311Asp)
n.461C>G
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.37731631G>TCA398746140HNF1Bc.1009C>A (p.His337Asn)
c.931C>A (p.His311Asn)
n.461C>A
17g.37731632dupCA913190765HNF1Bc.1009dup (p.His337ProfsTer23)
c.931dup (p.His311ProfsTer23)
n.461dup
c.1009dup (p.His337ProfsTer?)
c.1009dup (p.His337ProfsTer25)
 ClinVar dbSNP
17g.37731632G>ACA8518949HNF1Bc.1008C>T (p.His336=)
c.930C>T (p.His310=)
n.460C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37731632G>CCA398746146HNF1Bc.1008C>G (p.His336Gln)
c.930C>G (p.His310Gln)
n.460C>G
 ClinVar
17g.37731632G>TCA398746152HNF1Bc.1008C>A (p.His336Gln)
c.930C>A (p.His310Gln)
n.460C>A
17g.37731633T>ACA398746164HNF1Bc.1007A>T (p.His336Leu)
c.929A>T (p.His310Leu)
n.459A>T
17g.37731633T>CCA398746154HNF1Bc.1007A>G (p.His336Arg)
c.929A>G (p.His310Arg)
n.459A>G
 ClinVar gnomAD v4
17g.37731633T>GCA398746161HNF1Bc.1007A>C (p.His336Pro)
c.929A>C (p.His310Pro)
n.459A>C
17g.37731634G>ACA214343HNF1Bc.1006C>T (p.His336Tyr)
c.928C>T (p.His310Tyr)
n.458C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37731634G>CCA8518950HNF1Bc.1006C>G (p.His336Asp)
c.928C>G (p.His310Asp)
n.458C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37731634G>TCA8518951HNF1Bc.1006C>A (p.His336Asn)
c.928C>A (p.His310Asn)
n.458C>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37731639dupCA913190767HNF1Bc.1006dup (p.His336ProfsTer24)
c.928dup (p.His310ProfsTer24)
n.458dup
c.1006dup (p.His336ProfsTer?)
c.1006dup (p.His336ProfsTer26)
 ClinVar dbSNP
17g.37731639delCA913190766HNF1Bc.1006del (p.His336ThrfsTer?)
c.928del (p.His310ThrfsTer?)
n.458del
c.1006del (p.His336ThrfsTer22)
 ClinVar gnomAD v4
17g.37731635G>ACA8518953HNF1Bc.1005C>T (p.Pro335=)
c.927C>T (p.Pro309=)
n.457C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37731635G>CCA8518952HNF1Bc.1005C>G (p.Pro335=)
c.927C>G (p.Pro309=)
n.457C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.37731635G>TCA499602472HNF1Bc.1005C>A (p.Pro335=)
c.927C>A (p.Pro309=)
n.457C>A
17g.37731636G>ACA398746183HNF1Bc.1004C>T (p.Pro335Leu)
c.926C>T (p.Pro309Leu)
n.456C>T
 dbSNP gnomAD v4
17g.37731636G>CCA398746187HNF1Bc.1004C>G (p.Pro335Arg)
c.926C>G (p.Pro309Arg)
n.456C>G
 gnomAD v4
17g.37731636G>TCA398746185HNF1Bc.1004C>A (p.Pro335His)
c.926C>A (p.Pro309His)
n.456C>A
17g.37731637G>ACA8518954HNF1Bc.1003C>T (p.Pro335Ser)
c.925C>T (p.Pro309Ser)
n.455C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.37731637G>CCA398746199HNF1Bc.1003C>G (p.Pro335Ala)
c.925C>G (p.Pro309Ala)
n.455C>G
 gnomAD v4
17g.37731637G>TCA398746203HNF1Bc.1003C>A (p.Pro335Thr)
c.925C>A (p.Pro309Thr)
n.455C>A
17g.37731638G>ACA499602476HNF1Bc.1002C>T (p.Ser334=)
c.924C>T (p.Ser308=)
n.454C>T
17g.37731638G>CCA499602475HNF1Bc.1002C>G (p.Ser334=)
c.924C>G (p.Ser308=)
n.454C>G
17g.37731638G>TCA499602474HNF1Bc.1002C>A (p.Ser334=)
c.924C>A (p.Ser308=)
n.454C>A
 gnomAD v4
17g.37731639G>ACA398746206HNF1Bc.1001C>T (p.Ser334Phe)
c.923C>T (p.Ser308Phe)
n.453C>T
 ClinVar dbSNP gnomAD v4
17g.37731639G>CCA398746208HNF1Bc.1001C>G (p.Ser334Cys)
c.923C>G (p.Ser308Cys)
n.453C>G
17g.37731639G>TCA8518955HNF1Bc.1001C>A (p.Ser334Tyr)
c.923C>A (p.Ser308Tyr)
n.453C>A
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.37731640A>CCA398746213HNF1Bc.1000T>G (p.Ser334Ala)
c.922T>G (p.Ser308Ala)
n.452T>G
17g.37731640A>GCA398746217HNF1Bc.1000T>C (p.Ser334Pro)
c.922T>C (p.Ser308Pro)
n.452T>C
17g.37731640A>TCA398746222HNF1Bc.1000T>A (p.Ser334Thr)
c.922T>A (p.Ser308Thr)
n.452T>A
 gnomAD v4
17g.37731641G>ACA290281966HNF1Bc.999C>T (p.Gly333=)
c.921C>T (p.Gly307=)
n.451C>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
17g.37731641G>CCA499602478HNF1Bc.999C>G (p.Gly333=)
c.921C>G (p.Gly307=)
n.451C>G
17g.37731641G>TCA499602479HNF1Bc.999C>A (p.Gly333=)
c.921C>A (p.Gly307=)
n.451C>A
 gnomAD v4
17g.37731642C>ACA398746231HNF1Bc.998G>T (p.Gly333Val)
c.920G>T (p.Gly307Val)
n.450G>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
17g.37731642C>GCA398746229HNF1Bc.998G>C (p.Gly333Ala)
c.920G>C (p.Gly307Ala)
n.450G>C
17g.37731642C>TCA398746226HNF1Bc.998G>A (p.Gly333Asp)
c.920G>A (p.Gly307Asp)
n.450G>A
17g.37731643C>ACA398746242HNF1Bc.997G>T (p.Gly333Cys)
c.919G>T (p.Gly307Cys)
n.449G>T
 dbSNP gnomAD v2 gnomAD v4
17g.37731643C>GCA398746251HNF1Bc.997G>C (p.Gly333Arg)
c.919G>C (p.Gly307Arg)
n.449G>C
17g.37731643C>TCA8518956HNF1Bc.997G>A (p.Gly333Ser)
c.919G>A (p.Gly307Ser)
n.449G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37731644G>ACA8518957HNF1Bc.996C>T (p.His332=)
c.918C>T (p.His306=)
n.448C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37731644G>CCA398746273HNF1Bc.996C>G (p.His332Gln)
c.918C>G (p.His306Gln)
n.448C>G
17g.37731644G>TCA398746279HNF1Bc.996C>A (p.His332Gln)
c.918C>A (p.His306Gln)
n.448C>A
17g.37731645T>ACA398746283HNF1Bc.995A>T (p.His332Leu)
c.917A>T (p.His306Leu)
n.447A>T
17g.37731645T>CCA398746287HNF1Bc.995A>G (p.His332Arg)
c.917A>G (p.His306Arg)
n.447A>G
17g.37731645T>GCA398746289HNF1Bc.995A>C (p.His332Pro)
c.917A>C (p.His306Pro)
n.447A>C
17g.37731646G>ACA398746293HNF1Bc.994C>T (p.His332Tyr)
c.916C>T (p.His306Tyr)
n.446C>T
 dbSNP gnomAD v4
17g.37731646G>CCA398746294HNF1Bc.994C>G (p.His332Asp)
c.916C>G (p.His306Asp)
n.446C>G
17g.37731646G>TCA398746296HNF1Bc.994C>A (p.His332Asn)
c.916C>A (p.His306Asn)
n.446C>A
17g.37731647G>ACA8518958HNF1Bc.993C>T (p.Ser331=)
c.915C>T (p.Ser305=)
n.445C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37731647G>CCA499602485HNF1Bc.993C>G (p.Ser331=)
c.915C>G (p.Ser305=)
n.445C>G
17g.37731647G>TCA499602486HNF1Bc.993C>A (p.Ser331=)
c.915C>A (p.Ser305=)
n.445C>A
17g.37731648G>ACA398746299HNF1Bc.992C>T (p.Ser331Phe)
c.914C>T (p.Ser305Phe)
n.444C>T
17g.37731648G>CCA398746300HNF1Bc.992C>G (p.Ser331Cys)
c.914C>G (p.Ser305Cys)
n.444C>G
17g.37731648G>TCA398746302HNF1Bc.992C>A (p.Ser331Tyr)
c.914C>A (p.Ser305Tyr)
n.444C>A
17g.37731649A>CCA398746304HNF1Bc.991T>G (p.Ser331Ala)
c.913T>G (p.Ser305Ala)
n.443T>G
17g.37731649A>GCA398746307HNF1Bc.991T>C (p.Ser331Pro)
c.913T>C (p.Ser305Pro)
n.443T>C
17g.37731649A>TCA398746305HNF1Bc.991T>A (p.Ser331Thr)
c.913T>A (p.Ser305Thr)
n.443T>A
17g.37731650G>ACA290281984HNF1Bc.990C>T (p.Leu330=)
c.912C>T (p.Leu304=)
n.442C>T
 dbSNP gnomAD v4
17g.37731650G>CCA499602490HNF1Bc.990C>G (p.Leu330=)
c.912C>G (p.Leu304=)
n.442C>G
 dbSNP
17g.37731650G>TCA499602491HNF1Bc.990C>A (p.Leu330=)
c.912C>A (p.Leu304=)
n.442C>A
17g.37731651A>CCA398746309HNF1Bc.989T>G (p.Leu330Arg)
c.911T>G (p.Leu304Arg)
n.441T>G
17g.37731651A>GCA398746311HNF1Bc.989T>C (p.Leu330Pro)
c.911T>C (p.Leu304Pro)
n.441T>C
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.37731651A>TCA398746312HNF1Bc.989T>A (p.Leu330His)
c.911T>A (p.Leu304His)
n.441T>A
17g.37731652G>ACA8518959HNF1Bc.988C>T (p.Leu330Phe)
c.910C>T (p.Leu304Phe)
n.440C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37731652G>CCA398746315HNF1Bc.988C>G (p.Leu330Val)
c.910C>G (p.Leu304Val)
n.440C>G
17g.37731652G>TCA398746317HNF1Bc.988C>A (p.Leu330Ile)
c.910C>A (p.Leu304Ile)
n.440C>A
17g.37731653C>ACA499602497HNF1Bc.987G>T (p.Leu329=)
c.909G>T (p.Leu303=)
n.439G>T
17g.37731653C>GCA499602496HNF1Bc.987G>C (p.Leu329=)
c.909G>C (p.Leu303=)
n.439G>C
17g.37731653C>TCA499602495HNF1Bc.987G>A (p.Leu329=)
c.909G>A (p.Leu303=)
n.439G>A
 ClinVar dbSNP gnomAD v4
17g.37731654A>CCA398746319HNF1Bc.986T>G (p.Leu329Arg)
c.908T>G (p.Leu303Arg)
n.438T>G
17g.37731654A>GCA398746322HNF1Bc.986T>C (p.Leu329Pro)
c.908T>C (p.Leu303Pro)
n.438T>C
17g.37731654A>TCA398746323HNF1Bc.986T>A (p.Leu329Gln)
c.908T>A (p.Leu303Gln)
n.438T>A
17g.37731654_37731658delCA913190768HNF1Bc.982_986del (p.Pro328AlafsTer30)
c.904_908del (p.Pro302AlafsTer30)
n.434_438del
c.982_986del (p.Pro328AlafsTer?)
 ClinVar
17g.37731655G>ACA290281989HNF1Bc.985C>T (p.Leu329=)
c.907C>T (p.Leu303=)
n.437C>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.37731655G>CCA398746324HNF1Bc.985C>G (p.Leu329Val)
c.907C>G (p.Leu303Val)
n.437C>G
17g.37731655G>TCA398746329HNF1Bc.985C>A (p.Leu329Met)
c.907C>A (p.Leu303Met)
n.437C>A
17g.37731656A>CCA499602501HNF1Bc.984T>G (p.Pro328=)
c.906T>G (p.Pro302=)
n.436T>G
17g.37731656A>GCA499602500HNF1Bc.984T>C (p.Pro328=)
c.906T>C (p.Pro302=)
n.436T>C
17g.37731656A>TCA499602499HNF1Bc.984T>A (p.Pro328=)
c.906T>A (p.Pro302=)
n.436T>A
17g.37731657G>ACA8518960HNF1Bc.983C>T (p.Pro328Leu)
c.905C>T (p.Pro302Leu)
n.435C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37731657G>CCA398746334HNF1Bc.983C>G (p.Pro328Arg)
c.905C>G (p.Pro302Arg)
n.435C>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
17g.37731657G>TCA398746331HNF1Bc.983C>A (p.Pro328His)
c.905C>A (p.Pro302His)
n.435C>A
17g.37731659delCA913190769HNF1Bc.983del (p.Pro328LeufsTer?)
c.905del (p.Pro302LeufsTer?)
n.435del
c.983del (p.Pro328LeufsTer30)
 ClinVar
17g.37731658G>ACA290281999HNF1Bc.982C>T (p.Pro328Ser)
c.904C>T (p.Pro302Ser)
n.434C>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
17g.37731658G>CCA398746337HNF1Bc.982C>G (p.Pro328Ala)
c.904C>G (p.Pro302Ala)
n.434C>G
17g.37731658G>TCA398746340HNF1Bc.982C>A (p.Pro328Thr)
c.904C>A (p.Pro302Thr)
n.434C>A
 ClinVar dbSNP gnomAD v4
17g.37731659G>ACA499602502HNF1Bc.981C>T (p.Asn327=)
c.903C>T (p.Asn301=)
n.433C>T
 dbSNP gnomAD v2 gnomAD v4
17g.37731659G>CCA8518961HNF1Bc.981C>G (p.Asn327Lys)
c.903C>G (p.Asn301Lys)
n.433C>G
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37731659G>TCA398746351HNF1Bc.981C>A (p.Asn327Lys)
c.903C>A (p.Asn301Lys)
n.433C>A
17g.37731660T>ACA398746357HNF1Bc.980A>T (p.Asn327Ile)
c.902A>T (p.Asn301Ile)
n.432A>T
17g.37731660T>CCA8518962HNF1Bc.980A>G (p.Asn327Ser)
c.902A>G (p.Asn301Ser)
n.432A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.37731660T>GCA398746360HNF1Bc.980A>C (p.Asn327Thr)
c.902A>C (p.Asn301Thr)
n.432A>C
17g.37731661T>ACA398746363HNF1Bc.979A>T (p.Asn327Tyr)
c.901A>T (p.Asn301Tyr)
n.431A>T
c.882A>T (p.Ter294Cys)
17g.37731661T>CCA398746376HNF1Bc.979A>G (p.Asn327Asp)
c.901A>G (p.Asn301Asp)
n.431A>G
c.882A>G (p.Ter294Trp)
17g.37731661T>GCA398746379HNF1Bc.979A>C (p.Asn327His)
c.901A>C (p.Asn301His)
n.431A>C
c.882A>C (p.Ter294Cys)
17g.37731662C>ACA398746382HNF1Bc.978G>T (p.Leu326=)
c.900G>T (p.Leu300=)
n.430G>T
c.881G>T (p.Ter294Leu)
17g.37731662C>GCA290282006HNF1Bc.978G>C (p.Leu326=)
c.900G>C (p.Leu300=)
n.430G>C
c.881G>C (p.Ter294Ser)
 dbSNP gnomAD v4
17g.37731662C>TCA499602505HNF1Bc.978G>A (p.Leu326=)
c.900G>A (p.Leu300=)
n.430G>A
c.881G>A (p.Ter294=)
17g.37731663A>CCA398746388HNF1Bc.977T>G (p.Leu326Arg)
c.899T>G (p.Leu300Arg)
n.429T>G
c.880T>G (p.Ter294Gly)
17g.37731663A>GCA398746389HNF1Bc.977T>C (p.Leu326Pro)
c.899T>C (p.Leu300Pro)
n.429T>C
c.880T>C (p.Ter294Arg)
 gnomAD v4
17g.37731663A>TCA398746387HNF1Bc.977T>A (p.Leu326Gln)
c.899T>A (p.Leu300Gln)
n.429T>A
c.880T>A (p.Ter294Arg)
17g.37731664G>ACA499602506HNF1Bc.976C>T (p.Leu326=)
c.898C>T (p.Leu300=)
n.428C>T
c.879C>T (p.Ala293=)
17g.37731664G>CCA8518963HNF1Bc.976C>G (p.Leu326Val)
c.898C>G (p.Leu300Val)
n.428C>G
c.879C>G (p.Ala293=)
 dbSNP ExAC gnomAD v2
17g.37731664G>TCA398746390HNF1Bc.976C>A (p.Leu326Met)
c.898C>A (p.Leu300Met)
n.428C>A
c.879C>A (p.Ala293=)
17g.37731665G>ACA398746391HNF1Bc.975C>T (p.Ser325=)
c.897C>T (p.Ser299=)
n.427C>T
c.878C>T (p.Ala293Val)
17g.37731665G>CCA398746392HNF1Bc.975C>G (p.Ser325Arg)
c.897C>G (p.Ser299Arg)
n.427C>G
c.878C>G (p.Ala293Gly)
17g.37731665G>TCA398746393HNF1Bc.975C>A (p.Ser325Arg)
c.897C>A (p.Ser299Arg)
n.427C>A
c.878C>A (p.Ala293Asp)
17g.37731666C>ACA398746397HNF1Bc.974G>T (p.Ser325Ile)
c.896G>T (p.Ser299Ile)
n.426G>T
c.877G>T (p.Ala293Ser)
17g.37731666C>GCA398746395HNF1Bc.974G>C (p.Ser325Thr)
c.896G>C (p.Ser299Thr)
n.426G>C
c.877G>C (p.Ala293Pro)
17g.37731666C>TCA245115HNF1Bc.974G>A (p.Ser325Asn)
c.896G>A (p.Ser299Asn)
n.426G>A
c.877G>A (p.Ala293Thr)
 ClinVar dbSNP gnomAD v3 gnomAD v4
17g.37731667T>ACA398746400HNF1Bc.973A>T (p.Ser325Cys)
c.895A>T (p.Ser299Cys)
n.425A>T
c.876A>T (p.Thr292=)
17g.37731667T>CCA398746401HNF1Bc.973A>G (p.Ser325Gly)
c.895A>G (p.Ser299Gly)
n.425A>G
c.876A>G (p.Thr292=)
 gnomAD v4
17g.37731667T>GCA398746402HNF1Bc.973A>C (p.Ser325Arg)
c.895A>C (p.Ser299Arg)
n.425A>C
c.876A>C (p.Thr292=)
17g.37731669_37731670delCA913190770HNF1Bc.972_973del (p.His324GlnfsTer?)
c.894_895del (p.His298GlnfsTer?)
n.424_425del
c.875_876del (p.Thr292SerfsTer?)
 ClinVar
17g.37731668G>ACA398746403HNF1Bc.972C>T (p.His324=)
c.894C>T (p.His298=)
n.424C>T
c.875C>T (p.Thr292Ile)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.37731668G>CCA398746405HNF1Bc.972C>G (p.His324Gln)
c.894C>G (p.His298Gln)
n.424C>G
c.875C>G (p.Thr292Arg)
17g.37731668G>TCA8518964HNF1Bc.972C>A (p.His324Gln)
c.894C>A (p.His298Gln)
n.424C>A
c.875C>A (p.Thr292Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37731669T>ACA398746410HNF1Bc.971A>T (p.His324Leu)
c.893A>T (p.His298Leu)
n.423A>T
c.874A>T (p.Thr292Ser)
17g.37731669T>CCA398746411HNF1Bc.971A>G (p.His324Arg)
c.893A>G (p.His298Arg)
n.423A>G
c.874A>G (p.Thr292Ala)
17g.37731669T>GCA398746408HNF1Bc.971A>C (p.His324Pro)
c.893A>C (p.His298Pro)
n.423A>C
c.874A>C (p.Thr292Pro)
17g.37731670G>ACA398746412HNF1Bc.970C>T (p.His324Tyr)
c.892C>T (p.His298Tyr)
n.422C>T
c.873C>T (p.Leu291=)
17g.37731670G>CCA398746413HNF1Bc.970C>G (p.His324Asp)
c.892C>G (p.His298Asp)
n.422C>G
c.873C>G (p.Leu291=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.37731670G>TCA398746414HNF1Bc.970C>A (p.His324Asn)
c.892C>A (p.His298Asn)
n.422C>A
c.873C>A (p.Leu291=)
17g.37731671A>CCA398746415HNF1Bc.969T>G (p.Thr323=)
c.891T>G (p.Thr297=)
n.421T>G
c.872T>G (p.Leu291Arg)
17g.37731671A>GCA398746416HNF1Bc.969T>C (p.Thr323=)
c.891T>C (p.Thr297=)
n.421T>C
c.872T>C (p.Leu291Pro)
17g.37731671A>TCA398746417HNF1Bc.969T>A (p.Thr323=)
c.891T>A (p.Thr297=)
n.421T>A
c.872T>A (p.Leu291His)
17g.37731672G>ACA398746422HNF1Bc.968C>T (p.Thr323Ile)
c.890C>T (p.Thr297Ile)
n.420C>T
c.871C>T (p.Leu291Phe)
 dbSNP gnomAD v3 gnomAD v4
17g.37731672G>CCA8518965HNF1Bc.968C>G (p.Thr323Ser)
c.890C>G (p.Thr297Ser)
n.420C>G
c.871C>G (p.Leu291Val)
 dbSNP ExAC gnomAD v2 gnomAD v4
17g.37731672G>TCA398746419HNF1Bc.968C>A (p.Thr323Asn)
c.890C>A (p.Thr297Asn)
n.420C>A
c.871C>A (p.Leu291Ile)
17g.37731673T>ACA398746424HNF1Bc.967A>T (p.Thr323Ser)
c.889A>T (p.Thr297Ser)
n.419A>T
c.870A>T (p.Arg290Ser)
17g.37731673T>CCA398746426HNF1Bc.967A>G (p.Thr323Ala)
c.889A>G (p.Thr297Ala)
n.419A>G
c.870A>G (p.Arg290=)
17g.37731673T>GCA398746428HNF1Bc.967A>C (p.Thr323Pro)
c.889A>C (p.Thr297Pro)
n.419A>C
c.870A>C (p.Arg290Ser)
 gnomAD v4
17g.37731673dupCA913190771HNF1Bc.967dup (p.Thr323AsnfsTer?)
c.889dup (p.Thr297AsnfsTer?)
n.419dup
c.870dup (p.Leu291ThrfsTer?)
 ClinVar
17g.37731674C>ACA398746429HNF1Bc.966G>T (p.Gln322His)
c.888G>T (p.Gln296His)
n.418G>T
c.869G>T (p.Arg290Ile)
 dbSNP gnomAD v3 gnomAD v4
17g.37731674C>GCA398746430HNF1Bc.966G>C (p.Gln322His)
c.888G>C (p.Gln296His)
n.418G>C
c.869G>C (p.Arg290Thr)
 gnomAD v4
17g.37731674C>TCA398746431HNF1Bc.966G>A (p.Gln322=)
c.888G>A (p.Gln296=)
n.418G>A
c.869G>A (p.Arg290Lys)
 dbSNP gnomAD v2 gnomAD v4
17g.37731675T>ACA398746433HNF1Bc.965A>T (p.Gln322Leu)
c.887A>T (p.Gln296Leu)
n.417A>T
c.868A>T (p.Arg290Ter)
17g.37731675T>CCA398746439HNF1Bc.965A>G (p.Gln322Arg)
c.887A>G (p.Gln296Arg)
n.417A>G
c.868A>G (p.Arg290Gly)
17g.37731675T>GCA398746438HNF1Bc.965A>C (p.Gln322Pro)
c.887A>C (p.Gln296Pro)
n.417A>C
c.868A>C (p.Arg290=)
 gnomAD v4
17g.37731676G>ACA398746442HNF1Bc.964C>T (p.Gln322Ter)
c.886C>T (p.Gln296Ter)
n.416C>T
c.867C>T (p.Thr289=)
17g.37731676G>CCA398746443HNF1Bc.964C>G (p.Gln322Glu)
c.886C>G (p.Gln296Glu)
n.416C>G
c.867C>G (p.Thr289=)
17g.37731676G>TCA398746445HNF1Bc.964C>A (p.Gln322Lys)
c.886C>A (p.Gln296Lys)
n.416C>A
c.867C>A (p.Thr289=)
17g.37731677G>ACA398746450HNF1Bc.963C>T (p.Asn321=)
c.885C>T (p.Asn295=)
n.415C>T
c.866C>T (p.Thr289Ile)
 dbSNP gnomAD v4
17g.37731677G>CCA398746452HNF1Bc.963C>G (p.Asn321Lys)
c.885C>G (p.Asn295Lys)
n.415C>G
c.866C>G (p.Thr289Ser)
17g.37731677G>TCA398746454HNF1Bc.963C>A (p.Asn321Lys)
c.885C>A (p.Asn295Lys)
n.415C>A
c.866C>A (p.Thr289Asn)
17g.37731678T>ACA398746456HNF1Bc.962A>T (p.Asn321Ile)
c.884A>T (p.Asn295Ile)
n.414A>T
c.865A>T (p.Thr289Ser)
17g.37731678T>CCA214373HNF1Bc.962A>G (p.Asn321Ser)
c.884A>G (p.Asn295Ser)
n.414A>G
c.865A>G (p.Thr289Ala)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37731678T>GCA398746457HNF1Bc.962A>C (p.Asn321Thr)
c.884A>C (p.Asn295Thr)
n.414A>C
c.865A>C (p.Thr289Pro)
17g.37731679T>ACA398746458HNF1Bc.961A>T (p.Asn321Tyr)
c.883A>T (p.Asn295Tyr)
n.413A>T
c.864A>T (p.Pro288=)
17g.37731679T>CCA398746459HNF1Bc.961A>G (p.Asn321Asp)
c.883A>G (p.Asn295Asp)
n.413A>G
c.864A>G (p.Pro288=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
17g.37731679T>GCA398746461HNF1Bc.961A>C (p.Asn321His)
c.883A>C (p.Asn295His)
n.413A>C
c.864A>C (p.Pro288=)
 gnomAD v4
17g.37731680G>ACA398746463HNF1Bc.960C>T (p.Ser320=)
c.882C>T (p.Ser294=)
n.412C>T
c.863C>T (p.Pro288Leu)
17g.37731680G>CCA398746466HNF1Bc.960C>G (p.Ser320=)
c.882C>G (p.Ser294=)
n.412C>G
c.863C>G (p.Pro288Arg)
17g.37731680G>TCA398746465HNF1Bc.960C>A (p.Ser320=)
c.882C>A (p.Ser294=)
n.412C>A
c.863C>A (p.Pro288Gln)
17g.37731681G>ACA398746468HNF1Bc.959C>T (p.Ser320Phe)
c.881C>T (p.Ser294Phe)
n.411C>T
c.862C>T (p.Pro288Ser)
17g.37731681G>CCA398746470HNF1Bc.959C>G (p.Ser320Cys)
c.881C>G (p.Ser294Cys)
n.411C>G
c.862C>G (p.Pro288Ala)
17g.37731681G>TCA398746471HNF1Bc.959C>A (p.Ser320Tyr)
c.881C>A (p.Ser294Tyr)
n.411C>A
c.862C>A (p.Pro288Thr)
17g.37731682A>CCA398746473HNF1Bc.958T>G (p.Ser320Ala)
c.880T>G (p.Ser294Ala)
n.410T>G
c.861T>G (p.Ala287=)
17g.37731682A>GCA398746476HNF1Bc.958T>C (p.Ser320Pro)
c.880T>C (p.Ser294Pro)
n.410T>C
c.861T>C (p.Ala287=)
17g.37731682A>TCA398746478HNF1Bc.958T>A (p.Ser320Thr)
c.880T>A (p.Ser294Thr)
n.410T>A
c.861T>A (p.Ala287=)
 dbSNP gnomAD v2 gnomAD v4
17g.37731683G>ACA398746484HNF1Bc.957C>T (p.Ser319=)
c.879C>T (p.Ser293=)
n.409C>T
c.860C>T (p.Ala287Val)
17g.37731683G>CCA398746486HNF1Bc.957C>G (p.Ser319Arg)
c.879C>G (p.Ser293Arg)
n.409C>G
c.860C>G (p.Ala287Gly)
17g.37731683G>TCA398746488HNF1Bc.957C>A (p.Ser319Arg)
c.879C>A (p.Ser293Arg)
n.409C>A
c.860C>A (p.Ala287Asp)
17g.37731684C>ACA398746490HNF1Bc.956G>T (p.Ser319Ile)
c.878G>T (p.Ser293Ile)
n.408G>T
c.859G>T (p.Ala287Ser)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.37731684C>GCA398746492HNF1Bc.956G>C (p.Ser319Thr)
c.878G>C (p.Ser293Thr)
n.408G>C
c.859G>C (p.Ala287Pro)
17g.37731684C>TCA398746494HNF1Bc.956G>A (p.Ser319Asn)
c.878G>A (p.Ser293Asn)
n.408G>A
c.859G>A (p.Ala287Thr)
17g.37731685T>ACA398746505HNF1Bc.955A>T (p.Ser319Cys)
c.877A>T (p.Ser293Cys)
n.407A>T
c.858A>T (p.Ile286=)
17g.37731685T>CCA398746502HNF1Bc.955A>G (p.Ser319Gly)
c.877A>G (p.Ser293Gly)
n.407A>G
c.858A>G (p.Ile286Met)
17g.37731685T>GCA398746497HNF1Bc.955A>C (p.Ser319Arg)
c.877A>C (p.Ser293Arg)
n.407A>C
c.858A>C (p.Ile286=)
17g.37731686A>CCA398746508HNF1Bc.954T>G (p.Tyr318Ter)
c.876T>G (p.Tyr292Ter)
n.406T>G
c.857T>G (p.Ile286Arg)
17g.37731686A>GCA398746513HNF1Bc.954T>C (p.Tyr318=)
c.876T>C (p.Tyr292=)
n.406T>C
c.857T>C (p.Ile286Thr)
17g.37731686A>TCA398746515HNF1Bc.954T>A (p.Tyr318Ter)
c.876T>A (p.Tyr292Ter)
n.406T>A
c.857T>A (p.Ile286Lys)
17g.37731687T>ACA398746517HNF1Bc.953A>T (p.Tyr318Phe)
c.875A>T (p.Tyr292Phe)
n.405A>T
c.856A>T (p.Ile286Leu)
17g.37731687T>CCA8518966HNF1Bc.953A>G (p.Tyr318Cys)
c.875A>G (p.Tyr292Cys)
n.405A>G
c.856A>G (p.Ile286Val)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37731687T>GCA398746519HNF1Bc.953A>C (p.Tyr318Ser)
c.875A>C (p.Tyr292Ser)
n.405A>C
c.856A>C (p.Ile286Leu)
17g.37731687dupCA913190772HNF1Bc.953dup (p.Tyr318Ter)
c.875dup (p.Tyr292Ter)
n.405dup
c.856dup (p.Ile286AsnfsTer?)
 ClinVar
17g.37731688A>CCA398746521HNF1Bc.952T>G (p.Tyr318Asp)
c.874T>G (p.Tyr292Asp)
n.404T>G
c.855T>G (p.Pro285=)
17g.37731688A>GCA398746523HNF1Bc.952T>C (p.Tyr318His)
c.874T>C (p.Tyr292His)
n.404T>C
c.855T>C (p.Pro285=)
17g.37731688A>TCA398746524HNF1Bc.952T>A (p.Tyr318Asn)
c.874T>A (p.Tyr292Asn)
n.404T>A
c.855T>A (p.Pro285=)
17g.37731689G>ACA398746527HNF1Bc.951C>T (p.Ala317=)
c.873C>T (p.Ala291=)
n.403C>T
c.854C>T (p.Pro285Leu)
17g.37731689G>CCA214371HNF1Bc.951C>G (p.Ala317=)
c.873C>G (p.Ala291=)
n.403C>G
c.854C>G (p.Pro285Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37731689G>TCA398746529HNF1Bc.951C>A (p.Ala317=)
c.873C>A (p.Ala291=)
n.403C>A
c.854C>A (p.Pro285His)
17g.37731690G>ACA398746532HNF1Bc.950C>T (p.Ala317Val)
c.872C>T (p.Ala291Val)
n.402C>T
c.853C>T (p.Pro285Ser)
17g.37731690G>CCA398746539HNF1Bc.950C>G (p.Ala317Gly)
c.872C>G (p.Ala291Gly)
n.402C>G
c.853C>G (p.Pro285Ala)
17g.37731690G>TCA398746537HNF1Bc.950C>A (p.Ala317Asp)
c.872C>A (p.Ala291Asp)
n.402C>A
c.853C>A (p.Pro285Thr)
17g.37731691delCA913190773HNF1Bc.949del (p.Ala317ProfsTer10)
c.871del (p.Ala291ProfsTer10)
n.401del
c.852del (p.Pro285LeufsTer2)
 ClinVar
17g.37731691C>ACA214369HNF1Bc.949G>T (p.Ala317Ser)
c.871G>T (p.Ala291Ser)
n.401G>T
c.852G>T (p.Thr284=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
17g.37731691C>GCA398746543HNF1Bc.949G>C (p.Ala317Pro)
c.871G>C (p.Ala291Pro)
n.401G>C
c.852G>C (p.Thr284=)
17g.37731691C>TCA398746541HNF1Bc.949G>A (p.Ala317Thr)
c.871G>A (p.Ala291Thr)
n.401G>A
c.852G>A (p.Thr284=)
 dbSNP gnomAD v3 gnomAD v4
17g.37731692G>ACA8518967HNF1Bc.948C>T (p.Asp316=)
c.870C>T (p.Asp290=)
n.400C>T
c.851C>T (p.Thr284Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37731692G>CCA398746549HNF1Bc.948C>G (p.Asp316Glu)
c.870C>G (p.Asp290Glu)
n.400C>G
c.851C>G (p.Thr284Arg)
17g.37731692G>TCA398746547HNF1Bc.948C>A (p.Asp316Glu)
c.870C>A (p.Asp290Glu)
n.400C>A
c.851C>A (p.Thr284Lys)
17g.37731693T>ACA398746551HNF1Bc.947A>T (p.Asp316Val)
c.869A>T (p.Asp290Val)
n.399A>T
c.850A>T (p.Thr284Ser)
17g.37731693T>CCA398746553HNF1Bc.947A>G (p.Asp316Gly)
c.869A>G (p.Asp290Gly)
n.399A>G
c.850A>G (p.Thr284Ala)
17g.37731693T>GCA398746556HNF1Bc.947A>C (p.Asp316Ala)
c.869A>C (p.Asp290Ala)
n.399A>C
c.850A>C (p.Thr284Pro)
17g.37731694C>ACA398746558HNF1Bc.946G>T (p.Asp316Tyr)
c.868G>T (p.Asp290Tyr)
n.398G>T
c.849G>T (p.Trp283Cys)
17g.37731694C>GCA398746560HNF1Bc.946G>C (p.Asp316His)
c.868G>C (p.Asp290His)
n.398G>C
c.849G>C (p.Trp283Cys)
17g.37731694C>TCA398746562HNF1Bc.946G>A (p.Asp316Asn)
c.868G>A (p.Asp290Asn)
n.398G>A
c.849G>A (p.Trp283Ter)
17g.37731695C>ACA398746564HNF1Bc.945G>T (p.Met315Ile)
c.867G>T (p.Met289Ile)
n.397G>T
c.848G>T (p.Trp283Leu)
17g.37731695C>GCA398746565HNF1Bc.945G>C (p.Met315Ile)
c.867G>C (p.Met289Ile)
n.397G>C
c.848G>C (p.Trp283Ser)
17g.37731695C>TCA398746566HNF1Bc.945G>A (p.Met315Ile)
c.867G>A (p.Met289Ile)
n.397G>A
c.848G>A (p.Trp283Ter)
 dbSNP
17g.37731696A>CCA398746571HNF1Bc.944T>G (p.Met315Arg)
c.866T>G (p.Met289Arg)
n.396T>G
c.847T>G (p.Trp283Gly)
17g.37731696A>GCA8518968HNF1Bc.944T>C (p.Met315Thr)
c.866T>C (p.Met289Thr)
n.396T>C
c.847T>C (p.Trp283Arg)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37731696A>TCA398746573HNF1Bc.944T>A (p.Met315Lys)
c.866T>A (p.Met289Lys)
n.396T>A
c.847T>A (p.Trp283Arg)
17g.37731697T>ACA398746575HNF1Bc.943A>T (p.Met315Leu)
c.865A>T (p.Met289Leu)
n.395A>T
c.846A>T (p.Pro282=)
17g.37731697T>CCA398746578HNF1Bc.943A>G (p.Met315Val)
c.865A>G (p.Met289Val)
n.395A>G
c.846A>G (p.Pro282=)
 gnomAD v4
17g.37731697T>GCA398746577HNF1Bc.943A>C (p.Met315Leu)
c.865A>C (p.Met289Leu)
n.395A>C
c.846A>C (p.Pro282=)
17g.37731698G>ACA398746579HNF1Bc.942C>T (p.Ala314=)
c.864C>T (p.Ala288=)
n.394C>T
c.845C>T (p.Pro282Leu)
17g.37731698G>CCA398746580HNF1Bc.942C>G (p.Ala314=)
c.864C>G (p.Ala288=)
n.394C>G
c.845C>G (p.Pro282Arg)
17g.37731698G>TCA398746581HNF1Bc.942C>A (p.Ala314=)
c.864C>A (p.Ala288=)
n.394C>A
c.845C>A (p.Pro282Gln)
17g.37731699G>ACA398746583HNF1Bc.941C>T (p.Ala314Val)
c.863C>T (p.Ala288Val)
n.393C>T
c.844C>T (p.Pro282Ser)
17g.37731699G>CCA398746585HNF1Bc.941C>G (p.Ala314Gly)
c.863C>G (p.Ala288Gly)
n.393C>G
c.844C>G (p.Pro282Ala)
17g.37731699G>TCA398746588HNF1Bc.941C>A (p.Ala314Asp)
c.863C>A (p.Ala288Asp)
n.393C>A
c.844C>A (p.Pro282Thr)
17g.37731700C>ACA398746590HNF1Bc.940G>T (p.Ala314Ser)
c.862G>T (p.Ala288Ser)
n.392G>T
c.843G>T (p.Trp281Cys)
 dbSNP gnomAD v2
17g.37731700C>GCA398746592HNF1Bc.940G>C (p.Ala314Pro)
c.862G>C (p.Ala288Pro)
n.392G>C
c.843G>C (p.Trp281Cys)
17g.37731700C>TCA398746594HNF1Bc.940G>A (p.Ala314Thr)
c.862G>A (p.Ala288Thr)
n.392G>A
c.843G>A (p.Trp281Ter)
 ClinVar
17g.37731701delCA2560987073HNF1Bc.940del (p.Ala314ProfsTer13)
c.862del (p.Ala288ProfsTer13)
n.392del
c.843del (p.Trp281CysfsTer6)
17g.37731701C>ACA398746598HNF1Bc.939G>T (p.Leu313=)
c.861G>T (p.Leu287=)
n.391G>T
c.842G>T (p.Trp281Leu)
17g.37731701C>GCA398746602HNF1Bc.939G>C (p.Leu313=)
c.861G>C (p.Leu287=)
n.391G>C
c.842G>C (p.Trp281Ser)
17g.37731701C>TCA398746596HNF1Bc.939G>A (p.Leu313=)
c.861G>A (p.Leu287=)
n.391G>A
c.842G>A (p.Trp281Ter)

Number of alleles fetched