Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.37739503_37739577delCA913190793HNF1Bc.410_484del (p.Arg137_Lys161del)
ClinVar
17g.37739553C>ACA398751472HNF1Bc.431G>T (p.Gly144Val)
dbSNP
17g.37739553C>GCA398751474HNF1Bc.431G>C (p.Gly144Ala)
17g.37739553C>TCA398751475HNF1Bc.431G>A (p.Gly144Asp)
17g.37739554C>ACA398751480HNF1Bc.430G>T (p.Gly144Cys)
17g.37739554C>GCA398751478HNF1Bc.430G>C (p.Gly144Arg)
17g.37739554C>TCA8519075HNF1Bc.430G>A (p.Gly144Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37739555G>ACA8519076HNF1Bc.429C>T (p.Thr143=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37739555G>CCA499603947HNF1Bc.429C>G (p.Thr143=)
17g.37739555G>TCA499603948HNF1Bc.429C>A (p.Thr143=)
17g.37739556G>ACA398751485HNF1Bc.428C>T (p.Thr143Ile)
17g.37739556G>CCA398751482HNF1Bc.428C>G (p.Thr143Ser)
17g.37739556G>TCA398751483HNF1Bc.428C>A (p.Thr143Asn)
17g.37739557T>ACA398751487HNF1Bc.427A>T (p.Thr143Ser)
17g.37739557T>CCA398751488HNF1Bc.427A>G (p.Thr143Ala)
17g.37739557T>GCA398751490HNF1Bc.427A>C (p.Thr143Pro)
17g.37739558G>ACA499603949HNF1Bc.426C>T (p.Val142=)
dbSNP gnomAD v2 gnomAD v4
17g.37739558G>CCA499603950HNF1Bc.426C>G (p.Val142=)
17g.37739558G>TCA499603951HNF1Bc.426C>A (p.Val142=)
17g.37739559A>CCA398751493HNF1Bc.425T>G (p.Val142Gly)
17g.37739559A>GCA398751494HNF1Bc.425T>C (p.Val142Ala)
17g.37739559A>TCA398751495HNF1Bc.425T>A (p.Val142Asp)
17g.37739560C>ACA398751497HNF1Bc.424G>T (p.Val142Phe)
17g.37739560C>GCA398751499HNF1Bc.424G>C (p.Val142Leu)
17g.37739560C>TCA398751502HNF1Bc.424G>A (p.Val142Ile)
17g.37739561A>CCA398751504HNF1Bc.423T>G (p.Asp141Glu)
17g.37739561A>GCA499603952HNF1Bc.423T>C (p.Asp141=)
dbSNP
17g.37739561A>TCA398751505HNF1Bc.423T>A (p.Asp141Glu)
17g.37739562T>ACA398751508HNF1Bc.422A>T (p.Asp141Val)
17g.37739562T>CCA398751507HNF1Bc.422A>G (p.Asp141Gly)
17g.37739562T>GCA398751506HNF1Bc.422A>C (p.Asp141Ala)
17g.37739563C>ACA398751510HNF1Bc.421G>T (p.Asp141Tyr)
17g.37739563C>GCA398751512HNF1Bc.421G>C (p.Asp141His)
17g.37739563C>TCA290288699HNF1Bc.421G>A (p.Asp141Asn)
dbSNP gnomAD v4
17g.37739564G>ACA8519077HNF1Bc.420C>T (p.Val140=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37739564G>CCA499603953HNF1Bc.420C>G (p.Val140=)
17g.37739564G>TCA499603954HNF1Bc.420C>A (p.Val140=)
17g.37739565A>CCA398751514HNF1Bc.419T>G (p.Val140Gly)
17g.37739565A>GCA398751515HNF1Bc.419T>C (p.Val140Ala)
17g.37739565A>TCA398751516HNF1Bc.419T>A (p.Val140Asp)
17g.37739566C>ACA398751519HNF1Bc.418G>T (p.Val140Phe)
gnomAD v4
17g.37739566C>GCA398751520HNF1Bc.418G>C (p.Val140Leu)
17g.37739566C>TCA398751522HNF1Bc.418G>A (p.Val140Ile)
17g.37739567C>ACA499603955HNF1Bc.417G>T (p.Val139=)
17g.37739567C>GCA499603956HNF1Bc.417G>C (p.Val139=)
17g.37739567C>TCA499603957HNF1Bc.417G>A (p.Val139=)
17g.37739568A>CCA398751523HNF1Bc.416T>G (p.Val139Gly)
ClinVar
17g.37739568A>GCA398751525HNF1Bc.416T>C (p.Val139Ala)
gnomAD v4
17g.37739568A>TCA398751528HNF1Bc.416T>A (p.Val139Glu)
17g.37739569C>ACA398751532HNF1Bc.415G>T (p.Val139Leu)
17g.37739569C>GCA398751534HNF1Bc.415G>C (p.Val139Leu)
17g.37739569C>TCA398751530HNF1Bc.415G>A (p.Val139Met)
17g.37739570C>ACA398751536HNF1Bc.414G>T (p.Glu138Asp)
17g.37739570C>GCA398751537HNF1Bc.414G>C (p.Glu138Asp)
17g.37739570C>TCA499603958HNF1Bc.414G>A (p.Glu138=)
17g.37739571T>ACA398751538HNF1Bc.413A>T (p.Glu138Val)
17g.37739571T>CCA398751539HNF1Bc.413A>G (p.Glu138Gly)
17g.37739571T>GCA398751540HNF1Bc.413A>C (p.Glu138Ala)
17g.37739572C>ACA398751541HNF1Bc.412G>T (p.Glu138Ter)
17g.37739572C>GCA398751543HNF1Bc.412G>C (p.Glu138Gln)
17g.37739572C>TCA398751545HNF1Bc.412G>A (p.Glu138Lys)
17g.37739573C>ACA398751546HNF1Bc.411G>T (p.Arg137Ser)
17g.37739573C>GCA398751548HNF1Bc.411G>C (p.Arg137Ser)
17g.37739573C>TCA499603959HNF1Bc.411G>A (p.Arg137=)
17g.37739574C>ACA398751549HNF1Bc.410G>T (p.Arg137Met)
17g.37739574C>GCA398751551HNF1Bc.410G>C (p.Arg137Thr)
17g.37739574C>TCA398751552HNF1Bc.410G>A (p.Arg137Lys)
ClinVar dbSNP gnomAD v4
17g.37739575T>ACA398751554HNF1Bc.409A>T (p.Arg137Trp)
17g.37739575T>CCA398751555HNF1Bc.409A>G (p.Arg137Gly)
17g.37739575T>GCA499603960HNF1Bc.409A>C (p.Arg137=)
17g.37739576C>ACA398751557HNF1Bc.408G>T (p.Gln136His)
17g.37739576C>GCA398751559HNF1Bc.408G>C (p.Gln136His)
17g.37739576C>TCA499603961HNF1Bc.408G>A (p.Gln136=)
17g.37739577T>ACA398751561HNF1Bc.407A>T (p.Gln136Leu)
17g.37739577T>CCA398751562HNF1Bc.407A>G (p.Gln136Arg)
17g.37739577T>GCA398751564HNF1Bc.407A>C (p.Gln136Pro)
17g.37739578G>ACA398751565HNF1Bc.406C>T (p.Gln136Ter)
ClinVar
17g.37739578G>CCA398751567HNF1Bc.406C>G (p.Gln136Glu)
ClinVar
17g.37739578G>TCA398751568HNF1Bc.406C>A (p.Gln136Lys)
17g.37739582dupCA10603444HNF1Bc.406dup (p.Gln136ProfsTer?)
ClinVar dbSNP
17g.37739579G>ACA499603962HNF1Bc.405C>T (p.Pro135=)
17g.37739579G>CCA499603963HNF1Bc.405C>G (p.Pro135=)
17g.37739579G>TCA499603964HNF1Bc.405C>A (p.Pro135=)
17g.37739580G>ACA398751570HNF1Bc.404C>T (p.Pro135Leu)
17g.37739580G>CCA398751572HNF1Bc.404C>G (p.Pro135Arg)
17g.37739580G>TCA398751573HNF1Bc.404C>A (p.Pro135His)
17g.37739581G>ACA398751578HNF1Bc.403C>T (p.Pro135Ser)
17g.37739581G>CCA398751577HNF1Bc.403C>G (p.Pro135Ala)
17g.37739581G>TCA398751575HNF1Bc.403C>A (p.Pro135Thr)
17g.37739582G>ACA499603965HNF1Bc.402C>T (p.Ile134=)
ClinVar dbSNP gnomAD v4
17g.37739582G>CCA398751580HNF1Bc.402C>G (p.Ile134Met)
17g.37739582G>TCA499603966HNF1Bc.402C>A (p.Ile134=)
gnomAD v4
17g.37739583A>CCA398751585HNF1Bc.401T>G (p.Ile134Ser)
17g.37739583A>GCA398751582HNF1Bc.401T>C (p.Ile134Thr)
17g.37739583A>TCA398751583HNF1Bc.401T>A (p.Ile134Asn)
ClinVar dbSNP
17g.37739584T>ACA398751587HNF1Bc.400A>T (p.Ile134Phe)
17g.37739584T>CCA398751589HNF1Bc.400A>G (p.Ile134Val)
17g.37739584T>GCA398751590HNF1Bc.400A>C (p.Ile134Leu)
17g.37739585G>ACA499603967HNF1Bc.399C>T (p.Asn133=)
dbSNP
17g.37739585G>CCA398751591HNF1Bc.399C>G (p.Asn133Lys)
17g.37739585G>TCA398751593HNF1Bc.399C>A (p.Asn133Lys)
17g.37739586T>ACA398751595HNF1Bc.398A>T (p.Asn133Ile)
17g.37739586T>CCA398751597HNF1Bc.398A>G (p.Asn133Ser)
ClinVar
17g.37739586T>GCA398751598HNF1Bc.398A>C (p.Asn133Thr)
17g.37739587T>ACA398751600HNF1Bc.397A>T (p.Asn133Tyr)
17g.37739587T>CCA398751601HNF1Bc.397A>G (p.Asn133Asp)
17g.37739587T>GCA398751603HNF1Bc.397A>C (p.Asn133His)
17g.37739588G>ACA499603968HNF1Bc.396C>T (p.His132=)
17g.37739588G>CCA398751604HNF1Bc.396C>G (p.His132Gln)
dbSNP
17g.37739588G>TCA398751606HNF1Bc.396C>A (p.His132Gln)
17g.37739589T>ACA398751607HNF1Bc.395A>T (p.His132Leu)
17g.37739589T>CCA398751609HNF1Bc.395A>G (p.His132Arg)
ClinVar
17g.37739589T>GCA398751611HNF1Bc.395A>C (p.His132Pro)
ClinVar
17g.37739591_37739596delCA2695225795HNF1Bc.390_395del (p.Gln130_Gln131del)
17g.37739590G>ACA398751612HNF1Bc.394C>T (p.His132Tyr)
gnomAD v4
17g.37739590G>CCA398751613HNF1Bc.394C>G (p.His132Asp)
17g.37739590G>TCA398751615HNF1Bc.394C>A (p.His132Asn)
17g.37739591T>ACA398751616HNF1Bc.393A>T (p.Gln131His)
17g.37739591T>CCA499603969HNF1Bc.393A>G (p.Gln131=)
17g.37739591T>GCA398751617HNF1Bc.393A>C (p.Gln131His)
17g.37739592T>ACA398751619HNF1Bc.392A>T (p.Gln131Leu)
17g.37739592T>CCA398751620HNF1Bc.392A>G (p.Gln131Arg)
17g.37739592T>GCA398751622HNF1Bc.392A>C (p.Gln131Pro)
17g.37739594_37739600delCA913190796HNF1Bc.386_392del (p.Met129AsnfsTer15)
ClinVar
17g.37739593G>ACA398751625HNF1Bc.391C>T (p.Gln131Ter)
ClinVar
17g.37739593G>CCA398751626HNF1Bc.391C>G (p.Gln131Glu)
17g.37739593G>TCA398751624HNF1Bc.391C>A (p.Gln131Lys)
17g.37739594C>ACA398751628HNF1Bc.390G>T (p.Gln130His)
17g.37739594C>GCA398751629HNF1Bc.390G>C (p.Gln130His)
17g.37739594C>TCA499603970HNF1Bc.390G>A (p.Gln130=)
17g.37739595T>ACA398751632HNF1Bc.389A>T (p.Gln130Leu)
17g.37739595T>CCA398751633HNF1Bc.389A>G (p.Gln130Arg)
17g.37739595T>GCA398751634HNF1Bc.389A>C (p.Gln130Pro)
17g.37739596G>ACA398751640HNF1Bc.388C>T (p.Gln130Ter)
17g.37739596G>CCA398751638HNF1Bc.388C>G (p.Gln130Glu)
17g.37739596G>TCA398751636HNF1Bc.388C>A (p.Gln130Lys)
17g.37739597C>ACA398751641HNF1Bc.387G>T (p.Met129Ile)
17g.37739597C>GCA398751643HNF1Bc.387G>C (p.Met129Ile)
gnomAD v4
17g.37739597C>TCA398751645HNF1Bc.387G>A (p.Met129Ile)
dbSNP gnomAD v3 gnomAD v4
17g.37739598A>CCA398751647HNF1Bc.386T>G (p.Met129Arg)
17g.37739598A>GCA398751648HNF1Bc.386T>C (p.Met129Thr)
17g.37739598A>TCA398751649HNF1Bc.386T>A (p.Met129Lys)
17g.37739599T>ACA398751651HNF1Bc.385A>T (p.Met129Leu)
17g.37739599T>CCA398751654HNF1Bc.385A>G (p.Met129Val)
17g.37739599T>GCA398751653HNF1Bc.385A>C (p.Met129Leu)
17g.37739600G>ACA499603971HNF1Bc.384C>T (p.Tyr128=)
dbSNP gnomAD v3 gnomAD v4
17g.37739600G>CCA398751656HNF1Bc.384C>G (p.Tyr128Ter)
17g.37739600G>TCA398751658HNF1Bc.384C>A (p.Tyr128Ter)
17g.37739601T>ACA398751659HNF1Bc.383A>T (p.Tyr128Phe)
dbSNP
17g.37739601T>CCA398751660HNF1Bc.383A>G (p.Tyr128Cys)
17g.37739601T>GCA398751661HNF1Bc.383A>C (p.Tyr128Ser)
17g.37739602A>CCA398751663HNF1Bc.382T>G (p.Tyr128Asp)
17g.37739602A>GCA398751664HNF1Bc.382T>C (p.Tyr128His)
17g.37739602A>TCA398751665HNF1Bc.382T>A (p.Tyr128Asn)
17g.37739603dupCA983445274HNF1Bc.382dup (p.Tyr128LeufsTer?)
dbSNP gnomAD v3 gnomAD v4
17g.37739603A>CCA499603973HNF1Bc.381T>G (p.Gly127=)
17g.37739603A>GCA8519078HNF1Bc.381T>C (p.Gly127=)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.37739603A>TCA499603972HNF1Bc.381T>A (p.Gly127=)
17g.37739604C>ACA398751667HNF1Bc.380G>T (p.Gly127Val)
17g.37739604C>GCA398751668HNF1Bc.380G>C (p.Gly127Ala)
17g.37739604C>TCA398751670HNF1Bc.380G>A (p.Gly127Asp)
17g.37739605C>ACA398751673HNF1Bc.379G>T (p.Gly127Cys)
gnomAD v4
17g.37739605C>GCA398751675HNF1Bc.379G>C (p.Gly127Arg)
gnomAD v4
17g.37739605C>TCA398751672HNF1Bc.379G>A (p.Gly127Ser)
17g.37739606C>ACA398751679HNF1Bc.378G>T (p.Lys126Asn)
17g.37739606C>GCA398751677HNF1Bc.378G>C (p.Lys126Asn)
17g.37739606C>TCA499603974HNF1Bc.378G>A (p.Lys126=)
17g.37739607T>ACA398751684HNF1Bc.377A>T (p.Lys126Met)
17g.37739607T>CCA398751680HNF1Bc.377A>G (p.Lys126Arg)
gnomAD v4
17g.37739607T>GCA398751682HNF1Bc.377A>C (p.Lys126Thr)
17g.37739608T>ACA398751686HNF1Bc.376A>T (p.Lys126Ter)
17g.37739608T>CCA398751687HNF1Bc.376A>G (p.Lys126Glu)
ClinVar
17g.37739608T>GCA398751688HNF1Bc.376A>C (p.Lys126Gln)
17g.37739609G>ACA499603975HNF1Bc.375C>T (p.Ile125=)
17g.37739609G>CCA398751689HNF1Bc.375C>G (p.Ile125Met)
dbSNP
17g.37739609G>TCA8519079HNF1Bc.375C>A (p.Ile125=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.37739610A>CCA398751690HNF1Bc.374T>G (p.Ile125Ser)
17g.37739610A>GCA398751691HNF1Bc.374T>C (p.Ile125Thr)
ClinVar
17g.37739610A>TCA398751692HNF1Bc.374T>A (p.Ile125Asn)
ClinVar dbSNP
17g.37739611T>ACA398751693HNF1Bc.373A>T (p.Ile125Phe)
17g.37739611T>CCA398751694HNF1Bc.373A>G (p.Ile125Val)
17g.37739611T>GCA398751695HNF1Bc.373A>C (p.Ile125Leu)
17g.37739612C>ACA398751698HNF1Bc.372G>T (p.Met124Ile)
ClinVar
17g.37739612C>GCA398751697HNF1Bc.372G>C (p.Met124Ile)
17g.37739612C>TCA398751696HNF1Bc.372G>A (p.Met124Ile)
17g.37739613A>CCA398751699HNF1Bc.371T>G (p.Met124Arg)
17g.37739613A>GCA398751700HNF1Bc.371T>C (p.Met124Thr)
17g.37739613A>TCA398751701HNF1Bc.371T>A (p.Met124Lys)
17g.37739614T>ACA398751702HNF1Bc.370A>T (p.Met124Leu)
17g.37739614T>CCA398751703HNF1Bc.370A>G (p.Met124Val)
17g.37739614T>GCA398751704HNF1Bc.370A>C (p.Met124Leu)
17g.37739617delCA2695196522HNF1Bc.370del (p.Met124Ter)
17g.37739615T>ACA398751705HNF1Bc.369A>T (p.Lys123Asn)
17g.37739615T>CCA499603976HNF1Bc.369A>G (p.Lys123=)
17g.37739615T>GCA398751706HNF1Bc.369A>C (p.Lys123Asn)
17g.37739616T>ACA398751707HNF1Bc.368A>T (p.Lys123Ile)
17g.37739616T>CCA398751708HNF1Bc.368A>G (p.Lys123Arg)
17g.37739616T>GCA398751709HNF1Bc.368A>C (p.Lys123Thr)
17g.37739617T>ACA398751710HNF1Bc.367A>T (p.Lys123Ter)
17g.37739617T>CCA398751711HNF1Bc.367A>G (p.Lys123Glu)
17g.37739617T>GCA398751712HNF1Bc.367A>C (p.Lys123Gln)
17g.37739618A>CCA499603977HNF1Bc.366T>G (p.Ala122=)
17g.37739618A>GCA499603978HNF1Bc.366T>C (p.Ala122=)
dbSNP
17g.37739618A>TCA499603979HNF1Bc.366T>A (p.Ala122=)
17g.37739619G>ACA398751714HNF1Bc.365C>T (p.Ala122Val)
17g.37739619G>CCA398751715HNF1Bc.365C>G (p.Ala122Gly)
17g.37739619G>TCA398751713HNF1Bc.365C>A (p.Ala122Asp)
17g.37739620C>ACA398751716HNF1Bc.364G>T (p.Ala122Ser)
17g.37739620C>GCA398751717HNF1Bc.364G>C (p.Ala122Pro)
17g.37739620C>TCA398751718HNF1Bc.364G>A (p.Ala122Thr)
ClinVar dbSNP
17g.37739621A>CCA499603982HNF1Bc.363T>G (p.Ala121=)
17g.37739621A>GCA499603981HNF1Bc.363T>C (p.Ala121=)
17g.37739621A>TCA499603980HNF1Bc.363T>A (p.Ala121=)
17g.37739622G>ACA398751719HNF1Bc.362C>T (p.Ala121Val)
17g.37739622G>CCA398751720HNF1Bc.362C>G (p.Ala121Gly)
17g.37739622G>TCA398751721HNF1Bc.362C>A (p.Ala121Asp)
17g.37739623C>ACA398751722HNF1Bc.361G>T (p.Ala121Ser)
17g.37739623C>GCA398751723HNF1Bc.361G>C (p.Ala121Pro)
17g.37739623C>TCA398751724HNF1Bc.361G>A (p.Ala121Thr)
gnomAD v4
17g.37739624C>ACA398751725HNF1Bc.360G>T (p.Arg120Ser)
17g.37739624C>GCA398751726HNF1Bc.360G>C (p.Arg120Ser)
17g.37739624C>TCA499603983HNF1Bc.360G>A (p.Arg120=)
17g.37739625C>ACA398751729HNF1Bc.359G>T (p.Arg120Met)
17g.37739625C>GCA398751728HNF1Bc.359G>C (p.Arg120Thr)
17g.37739625C>TCA398751727HNF1Bc.359G>A (p.Arg120Lys)
17g.37739626T>ACA398751730HNF1Bc.358A>T (p.Arg120Trp)
17g.37739626T>CCA398751731HNF1Bc.358A>G (p.Arg120Gly)
dbSNP gnomAD v3 gnomAD v4
17g.37739626T>GCA499603984HNF1Bc.358A>C (p.Arg120=)
17g.37739627C>ACA398751732HNF1Bc.357G>T (p.Trp119Cys)
17g.37739627C>GCA398751733HNF1Bc.357G>C (p.Trp119Cys)
17g.37739627C>TCA398751734HNF1Bc.357G>A (p.Trp119Ter)
17g.37739628C>ACA398751735HNF1Bc.356G>T (p.Trp119Leu)
17g.37739628C>GCA398751736HNF1Bc.356G>C (p.Trp119Ser)
17g.37739628C>TCA398751737HNF1Bc.356G>A (p.Trp119Ter)
ClinVar
17g.37739629A>CCA398751738HNF1Bc.355T>G (p.Trp119Gly)
17g.37739629A>GCA398751739HNF1Bc.355T>C (p.Trp119Arg)
17g.37739629A>TCA398751740HNF1Bc.355T>A (p.Trp119Arg)
17g.37739630A>CCA499603985HNF1Bc.354T>G (p.Pro118=)
17g.37739630A>GCA8519080HNF1Bc.354T>C (p.Pro118=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37739630A>TCA499603986HNF1Bc.354T>A (p.Pro118=)
17g.37739631G>ACA398751743HNF1Bc.353C>T (p.Pro118Leu)
17g.37739631G>CCA398751742HNF1Bc.353C>G (p.Pro118Arg)
17g.37739631G>TCA398751741HNF1Bc.353C>A (p.Pro118His)
gnomAD v3 gnomAD v4
17g.37739633delCA913190797HNF1Bc.353del (p.Pro118LeufsTer7)
ClinVar
17g.37739632G>ACA398751744HNF1Bc.352C>T (p.Pro118Ser)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.37739632G>CCA398751745HNF1Bc.352C>G (p.Pro118Ala)
ClinVar dbSNP gnomAD v3 gnomAD v4
17g.37739632G>TCA8519081HNF1Bc.352C>A (p.Pro118Thr)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.37739633G>ACA499603987HNF1Bc.351C>T (p.Asp117=)
gnomAD v4
17g.37739633G>CCA398751746HNF1Bc.351C>G (p.Asp117Glu)
17g.37739633G>TCA398751747HNF1Bc.351C>A (p.Asp117Glu)
17g.37739634T>ACA290288735HNF1Bc.350A>T (p.Asp117Val)
dbSNP gnomAD v3 gnomAD v4
17g.37739634T>CCA398751748HNF1Bc.350A>G (p.Asp117Gly)
17g.37739634T>GCA398751749HNF1Bc.350A>C (p.Asp117Ala)
17g.37739635C>ACA398751750HNF1Bc.349G>T (p.Asp117Tyr)
17g.37739635C>GCA398751751HNF1Bc.349G>C (p.Asp117His)
17g.37739635C>TCA398751752HNF1Bc.349G>A (p.Asp117Asn)
17g.37739636C>ACA398751753HNF1Bc.348G>T (p.Glu116Asp)
gnomAD v4
17g.37739636C>GCA398751754HNF1Bc.348G>C (p.Glu116Asp)
17g.37739636C>TCA499603988HNF1Bc.348G>A (p.Glu116=)
17g.37739637T>ACA398751755HNF1Bc.347A>T (p.Glu116Val)
gnomAD v4
17g.37739637T>CCA398751756HNF1Bc.347A>G (p.Glu116Gly)
17g.37739637T>GCA398751757HNF1Bc.347A>C (p.Glu116Ala)
17g.37739638C>ACA398751758HNF1Bc.346G>T (p.Glu116Ter)
17g.37739638C>GCA398751760HNF1Bc.346G>C (p.Glu116Gln)
17g.37739638C>TCA398751759HNF1Bc.346G>A (p.Glu116Lys)
17g.37739639A>CCA398751761HNF1Bc.345T>G (p.Ser115Arg)
17g.37739639A>GCA499603992HNF1Bc.345T>C (p.Ser115=)
17g.37739639A>TCA398751762HNF1Bc.345T>A (p.Ser115Arg)
17g.37739640C>ACA214359HNF1Bc.345-1G>T (n.345-1G>T)
ClinVar dbSNP
17g.37739640C>GCA398751763HNF1Bc.345-1G>C (n.345-1G>C)
17g.37739640C>TCA398751764HNF1Bc.345-1G>A (n.345-1G>A)
ClinVar
17g.37739641T>ACA398751765HNF1Bc.345-2A>T (n.345-2A>T)
17g.37739641T>CCA398751766HNF1Bc.345-2A>G (n.345-2A>G)
ClinVar
17g.37739641T>GCA398751767HNF1Bc.345-2A>C (n.345-2A>C)
17g.37739643G>ACA8519082HNF1Bc.345-4C>T (n.345-4C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37739643G>CCA626207311HNF1Bc.345-4C>G (n.345-4C>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.37739643G>TCA2637449190HNF1Bc.345-4C>A (n.345-4C>A)
gnomAD v4
17g.37739644A>GCA2576244088HNF1Bc.345-5T>C (n.345-5T>C)
17g.37739645C>GCA290288748HNF1Bc.345-6G>C (n.345-6G>C)
dbSNP
17g.37739646_37739647insAACA626207312HNF1Bc.345-7_345-6insTT (n.345-7_345-6insTT)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.37739647G>CCA2739267525HNF1Bc.345-8C>G (n.345-8C>G)
ClinVar
17g.37739650A>CCA8519083HNF1Bc.345-11T>G (n.345-11T>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37739651A>TCA771674479HNF1Bc.345-12T>A (n.345-12T>A)
dbSNP
17g.37739651_37739663delCA2580093615HNF1Bc.345-24_345-12del (n.345-24_345-12del)
ClinVar
17g.37739652G>ACA626207313HNF1Bc.345-13C>T (n.345-13C>T)
dbSNP gnomAD v2 gnomAD v4
17g.37739653C>GCA2576244089HNF1Bc.345-14G>C (n.345-14G>C)
gnomAD v4
17g.37739653C>TCA8519084HNF1Bc.345-14G>A (n.345-14G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched