Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.37731580C>TCA625879228HNF1Bc.1045+15G>A (n.1045+15G>A)
c.967+15G>A (n.967+15G>A)
n.512G>A
 dbSNP gnomAD v2 gnomAD v4
17g.37731581C>TCA2637448704HNF1Bc.1045+14G>A (n.1045+14G>A)
c.967+14G>A (n.967+14G>A)
n.511G>A
 gnomAD v4
17g.37731583A>GCA214345HNF1Bc.1045+12T>C (n.1045+12T>C)
c.967+12T>C (n.967+12T>C)
n.509T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37731584C>ACA771701657HNF1Bc.1045+11G>T (n.1045+11G>T)
c.967+11G>T (n.967+11G>T)
n.508G>T
 dbSNP gnomAD v3 gnomAD v4
17g.37731584C>TCA8518945HNF1Bc.1045+11G>A (n.1045+11G>A)
c.967+11G>A (n.967+11G>A)
n.508G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37731585C>TCA983442060HNF1Bc.1045+10G>A (n.1045+10G>A)
c.967+10G>A (n.967+10G>A)
n.507G>A
 dbSNP gnomAD v3 gnomAD v4
17g.37731586T>GCA2637448705HNF1Bc.1045+9A>C (n.1045+9A>C)
c.967+9A>C (n.967+9A>C)
n.506A>C
 dbSNP gnomAD v4
17g.37731589G>ACA2576244014HNF1Bc.1045+6C>T (n.1045+6C>T)
c.967+6C>T (n.967+6C>T)
n.503C>T
 ClinVar gnomAD v4
17g.37731593A>CCA398745791HNF1Bc.1045+2T>G (n.1045+2T>G)
c.967+2T>G (n.967+2T>G)
n.499T>G
17g.37731593A>GCA398745794HNF1Bc.1045+2T>C (n.1045+2T>C)
c.967+2T>C (n.967+2T>C)
n.499T>C
17g.37731593A>TCA398745795HNF1Bc.1045+2T>A (n.1045+2T>A)
c.967+2T>A (n.967+2T>A)
n.499T>A
17g.37731594C>ACA398745796HNF1Bc.1045+1G>T (n.1045+1G>T)
c.967+1G>T (n.967+1G>T)
n.498G>T
17g.37731594C>GCA398745798HNF1Bc.1045+1G>C (n.1045+1G>C)
c.967+1G>C (n.967+1G>C)
n.498G>C
17g.37731594C>TCA398745801HNF1Bc.1045+1G>A (n.1045+1G>A)
c.967+1G>A (n.967+1G>A)
n.498G>A
 ClinVar
17g.37731598_37731833delCA913190764HNF1Bc.811_1045+1del
c.733_967+1del
n.263_498del
 ClinVar
17g.37731595C>ACA398745828HNF1Bc.1045G>T (p.Gly349Ter)
c.967G>T (p.Gly323Ter)
n.497G>T
c.1045G>T (p.Gly349Cys)
17g.37731595C>GCA398745823HNF1Bc.1045G>C (p.Gly349Arg)
c.967G>C (p.Gly323Arg)
n.497G>C
17g.37731595C>TCA398745808HNF1Bc.1045G>A (p.Gly349Arg)
c.967G>A (p.Gly323Arg)
n.497G>A
c.1045G>A (p.Gly349Ser)
17g.37731599_37733825delCA915950000HNF1Bc.545_1045del
c.545-78_967del
17g.37731596T>ACA499602422HNF1Bc.1044A>T (p.Ser348=)
c.966A>T (p.Ser322=)
n.496A>T
17g.37731596T>CCA499602423HNF1Bc.1044A>G (p.Ser348=)
c.966A>G (p.Ser322=)
n.496A>G
17g.37731596T>GCA499602424HNF1Bc.1044A>C (p.Ser348=)
c.966A>C (p.Ser322=)
n.496A>C
17g.37731597G>ACA398745834HNF1Bc.1043C>T (p.Ser348Leu)
c.965C>T (p.Ser322Leu)
n.495C>T
17g.37731597G>CCA398745839HNF1Bc.1043C>G (p.Ser348Ter)
c.965C>G (p.Ser322Ter)
n.495C>G
17g.37731597G>TCA398745842HNF1Bc.1043C>A (p.Ser348Ter)
c.965C>A (p.Ser322Ter)
n.495C>A
17g.37731598delCA2740095324HNF1Bc.1042del (p.Ser348GlnfsTer28)
c.964del (p.Ser322GlnfsTer28)
n.494del
c.1042del (p.Ser348GlnfsTer10)
c.1042del (p.Ser348GlnfsTer?)
 ClinVar
17g.37731598A>CCA398745846HNF1Bc.1042T>G (p.Ser348Ala)
c.964T>G (p.Ser322Ala)
n.494T>G
17g.37731598A>GCA398745849HNF1Bc.1042T>C (p.Ser348Pro)
c.964T>C (p.Ser322Pro)
n.494T>C
17g.37731598A>TCA398745852HNF1Bc.1042T>A (p.Ser348Thr)
c.964T>A (p.Ser322Thr)
n.494T>A
17g.37731599C>ACA499602425HNF1Bc.1041G>T (p.Leu347=)
c.963G>T (p.Leu321=)
n.493G>T
17g.37731599C>GCA499602426HNF1Bc.1041G>C (p.Leu347=)
c.963G>C (p.Leu321=)
n.493G>C
17g.37731599C>TCA499602427HNF1Bc.1041G>A (p.Leu347=)
c.963G>A (p.Leu321=)
n.493G>A
 gnomAD v4
17g.37731600A>CCA398745857HNF1Bc.1040T>G (p.Leu347Arg)
c.962T>G (p.Leu321Arg)
n.492T>G
 dbSNP gnomAD v2 gnomAD v4
17g.37731600A>GCA290281916HNF1Bc.1040T>C (p.Leu347Pro)
c.962T>C (p.Leu321Pro)
n.492T>C
 dbSNP
17g.37731600A>TCA398745859HNF1Bc.1040T>A (p.Leu347Gln)
c.962T>A (p.Leu321Gln)
n.492T>A
 gnomAD v4
17g.37731600dupCA2637448706HNF1Bc.1040dup (p.Ser348ValfsTer12)
c.962dup (p.Ser322ValfsTer12)
n.492dup
c.1040dup (p.Ser348ValfsTer?)
c.1040dup (p.Ser348ValfsTer14)
 gnomAD v4
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)

Number of alleles fetched