17 | g.37744664_37744682del | CA983447806 | HNF1B | c.204_222del (p.His69ProfsTer?)
| gnomAD v3 gnomAD v4 |
17 | g.37744664A>C | CA398753761 | HNF1B | c.221T>G (p.Leu74Trp)
| ClinVar dbSNP gnomAD v4 |
17 | g.37744664A>G | CA398753764 | HNF1B | c.221T>C (p.Leu74Ser)
| |
17 | g.37744664A>T | CA214355 | HNF1B | c.221T>A (p.Leu74Ter)
| ClinVar dbSNP |
17 | g.37744665A>C | CA398753771 | HNF1B | c.220T>G (p.Leu74Val)
| |
17 | g.37744665A>G | CA499880103 | HNF1B | c.220T>C (p.Leu74=)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37744665A>T | CA398753773 | HNF1B | c.220T>A (p.Leu74Met)
| |
17 | g.37744666G>A | CA499880105 | HNF1B | c.219C>T (p.Arg73=)
| |
17 | g.37744666G>C | CA499880106 | HNF1B | c.219C>G (p.Arg73=)
| |
17 | g.37744666G>T | CA499880107 | HNF1B | c.219C>A (p.Arg73=)
| |
17 | g.37744667C>A | CA398753777 | HNF1B | c.218G>T (p.Arg73Leu)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.37744667C>G | CA398753780 | HNF1B | c.218G>C (p.Arg73Pro)
| gnomAD v4 |
17 | g.37744667C>T | CA398753783 | HNF1B | c.218G>A (p.Arg73His)
| |
17 | g.37744667_37744674del | CA913186015 | HNF1B | c.211_218del (p.Lys71LeufsTer14)
| |
17 | g.37744668G>A | CA398753786 | HNF1B | c.217C>T (p.Arg73Cys)
| dbSNP gnomAD v4 |
17 | g.37744668G>C | CA398753788 | HNF1B | c.217C>G (p.Arg73Gly)
| gnomAD v4 |
17 | g.37744668G>T | CA398753791 | HNF1B | c.217C>A (p.Arg73Ser)
| |
17 | g.37744671_37744677del | CA913190803 | HNF1B | c.211_217del (p.Lys71AlafsTer?)
| ClinVar |
17 | g.37744669G>A | CA499880109 | HNF1B | c.216C>T (p.Gly72=)
| |
17 | g.37744669G>C | CA499880110 | HNF1B | c.216C>G (p.Gly72=)
| |
17 | g.37744669G>T | CA499880111 | HNF1B | c.216C>A (p.Gly72=)
| gnomAD v4 |
17 | g.37744670C>A | CA398753796 | HNF1B | c.215G>T (p.Gly72Val)
| dbSNP gnomAD v2 |
17 | g.37744670C>G | CA398753800 | HNF1B | c.215G>C (p.Gly72Ala)
| |
17 | g.37744670C>T | CA398753813 | HNF1B | c.215G>A (p.Gly72Asp)
| dbSNP gnomAD v4 |
17 | g.37744672del | CA2582343037 | HNF1B | c.215del (p.Gly72AlafsTer?)
| ClinVar |
17 | g.37744671C>A | CA398753817 | HNF1B | c.214G>T (p.Gly72Cys)
| gnomAD v4 |
17 | g.37744671C>G | CA398753820 | HNF1B | c.214G>C (p.Gly72Arg)
| |
17 | g.37744671C>T | CA398753822 | HNF1B | c.214G>A (p.Gly72Ser)
| |
17 | g.37744672C>A | CA398753830 | HNF1B | c.213G>T (p.Lys71Asn)
| dbSNP gnomAD v2 |
17 | g.37744672C>G | CA398753827 | HNF1B | c.213G>C (p.Lys71Asn)
| dbSNP gnomAD v2 gnomAD v4 |
17 | g.37744672C>T | CA499880113 | HNF1B | c.213G>A (p.Lys71=)
| |
17 | g.37744673T>A | CA398753831 | HNF1B | c.212A>T (p.Lys71Met)
| |
17 | g.37744673T>C | CA398753833 | HNF1B | c.212A>G (p.Lys71Arg)
| |
17 | g.37744673T>G | CA398753836 | HNF1B | c.212A>C (p.Lys71Thr)
| |
17 | g.37744674T>A | CA398753841 | HNF1B | c.211A>T (p.Lys71Ter)
| |
17 | g.37744674T>C | CA398753844 | HNF1B | c.211A>G (p.Lys71Glu)
| |
17 | g.37744674T>G | CA398753845 | HNF1B | c.211A>C (p.Lys71Gln)
| |
17 | g.37744678_37744682del | CA913190804 | HNF1B | c.207_211del (p.His69GlnfsTer17)
| ClinVar |
17 | g.37744675G>A | CA499880115 | HNF1B | c.210C>T (p.Ala70=)
| |
17 | g.37744675G>C | CA499880116 | HNF1B | c.210C>G (p.Ala70=)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37744675G>T | CA499880117 | HNF1B | c.210C>A (p.Ala70=)
| |
17 | g.37744676G>A | CA8519131 | HNF1B | c.209C>T (p.Ala70Val)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.37744676G>C | CA398753846 | HNF1B | c.209C>G (p.Ala70Gly)
| |
17 | g.37744676G>T | CA398753849 | HNF1B | c.209C>A (p.Ala70Asp)
| gnomAD v4 |
17 | g.37744677C>A | CA8519132 | HNF1B | c.208G>T (p.Ala70Ser)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37744677C>G | CA398753852 | HNF1B | c.208G>C (p.Ala70Pro)
| |
17 | g.37744677C>T | CA398753855 | HNF1B | c.208G>A (p.Ala70Thr)
| |
17 | g.37744678G>A | CA499880122 | HNF1B | c.207C>T (p.His69=)
| dbSNP gnomAD v4 |
17 | g.37744678G>C | CA398753856 | HNF1B | c.207C>G (p.His69Gln)
| |
17 | g.37744678G>T | CA398753857 | HNF1B | c.207C>A (p.His69Gln)
| |
17 | g.37744679_37744680del | CA913190805 | HNF1B | c.206_207del (p.His69ArgfsTer18)
| ClinVar |
17 | g.37744679T>A | CA398753864 | HNF1B | c.206A>T (p.His69Leu)
| |
17 | g.37744679T>C | CA398753861 | HNF1B | c.206A>G (p.His69Arg)
| gnomAD v4 |
17 | g.37744679T>G | CA398753859 | HNF1B | c.206A>C (p.His69Pro)
| |
17 | g.37744680G>A | CA398753868 | HNF1B | c.205C>T (p.His69Tyr)
| dbSNP gnomAD v3 gnomAD v4 |
17 | g.37744680G>C | CA398753870 | HNF1B | c.205C>G (p.His69Asp)
| |
17 | g.37744680G>T | CA398753873 | HNF1B | c.205C>A (p.His69Asn)
| |
17 | g.37744681G>A | CA499880126 | HNF1B | c.204C>T (p.Gly68=)
| |
17 | g.37744681G>C | CA499880125 | HNF1B | c.204C>G (p.Gly68=)
| |
17 | g.37744681G>T | CA499880124 | HNF1B | c.204C>A (p.Gly68=)
| |
17 | g.37744682C>A | CA398753875 | HNF1B | c.203G>T (p.Gly68Val)
| |
17 | g.37744682C>G | CA398753878 | HNF1B | c.203G>C (p.Gly68Ala)
| dbSNP gnomAD v3 gnomAD v4 |
17 | g.37744682C>T | CA398753882 | HNF1B | c.203G>A (p.Gly68Asp)
| |
17 | g.37744683C>A | CA398753884 | HNF1B | c.202G>T (p.Gly68Cys)
| gnomAD v4 |
17 | g.37744683C>G | CA8519133 | HNF1B | c.202G>C (p.Gly68Arg)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37744683C>T | CA398753889 | HNF1B | c.202G>A (p.Gly68Ser)
| gnomAD v4 |
17 | g.37744684G>A | CA499880130 | HNF1B | c.201C>T (p.Asn67=)
| dbSNP gnomAD v2 gnomAD v4 |
17 | g.37744684G>C | CA398753890 | HNF1B | c.201C>G (p.Asn67Lys)
| |
17 | g.37744684G>T | CA398753893 | HNF1B | c.201C>A (p.Asn67Lys)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37744685T>A | CA398753895 | HNF1B | c.200A>T (p.Asn67Ile)
| |
17 | g.37744685T>C | CA398753896 | HNF1B | c.200A>G (p.Asn67Ser)
| dbSNP |
17 | g.37744685T>G | CA398753902 | HNF1B | c.200A>C (p.Asn67Thr)
| |
17 | g.37744686T>A | CA398753909 | HNF1B | c.199A>T (p.Asn67Tyr)
| dbSNP gnomAD v4 |
17 | g.37744686T>C | CA398753912 | HNF1B | c.199A>G (p.Asn67Asp)
| |
17 | g.37744686T>G | CA398753906 | HNF1B | c.199A>C (p.Asn67His)
| |
17 | g.37744687G>A | CA499880132 | HNF1B | c.198C>T (p.Thr66=)
| |
17 | g.37744687G>C | CA499880133 | HNF1B | c.198C>G (p.Thr66=)
| |
17 | g.37744687G>T | CA499880134 | HNF1B | c.198C>A (p.Thr66=)
| |
17 | g.37744688G>A | CA398753916 | HNF1B | c.197C>T (p.Thr66Ile)
| |
17 | g.37744688G>C | CA398753919 | HNF1B | c.197C>G (p.Thr66Ser)
| |
17 | g.37744688G>T | CA398753923 | HNF1B | c.197C>A (p.Thr66Asn)
| |
17 | g.37744690_37744695del | CA2637449434 | HNF1B | c.192_197del (p.Leu65_Thr66del)
| gnomAD v4 |
17 | g.37744689T>A | CA398753928 | HNF1B | c.196A>T (p.Thr66Ser)
| |
17 | g.37744689T>C | CA398753949 | HNF1B | c.196A>G (p.Thr66Ala)
| gnomAD v4 |
17 | g.37744689T>G | CA398753952 | HNF1B | c.196A>C (p.Thr66Pro)
| |
17 | g.37744690G>A | CA499880138 | HNF1B | c.195C>T (p.Leu65=)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.37744690G>C | CA499880139 | HNF1B | c.195C>G (p.Leu65=)
| |
17 | g.37744690G>T | CA499880140 | HNF1B | c.195C>A (p.Leu65=)
| |
17 | g.37744691A>C | CA398753956 | HNF1B | c.194T>G (p.Leu65Arg)
| |
17 | g.37744691A>G | CA398753960 | HNF1B | c.194T>C (p.Leu65Pro)
| |
17 | g.37744691A>T | CA398753967 | HNF1B | c.194T>A (p.Leu65His)
| |
17 | g.37744692G>A | CA398753971 | HNF1B | c.193C>T (p.Leu65Phe)
| dbSNP gnomAD v2 gnomAD v4 |
17 | g.37744692G>C | CA398753972 | HNF1B | c.193C>G (p.Leu65Val)
| gnomAD v4 |
17 | g.37744692G>T | CA398753973 | HNF1B | c.193C>A (p.Leu65Ile)
| |
17 | g.37744693A>C | CA499880144 | HNF1B | c.192T>G (p.Thr64=)
| |
17 | g.37744693A>G | CA499880143 | HNF1B | c.192T>C (p.Thr64=)
| |
17 | g.37744693A>T | CA499880142 | HNF1B | c.192T>A (p.Thr64=)
| |
17 | g.37744694G>A | CA398753977 | HNF1B | c.191C>T (p.Thr64Ile)
| gnomAD v4 |
17 | g.37744694G>C | CA8519134 | HNF1B | c.191C>G (p.Thr64Ser)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37744694G>T | CA398753974 | HNF1B | c.191C>A (p.Thr64Asn)
| |
17 | g.37744695_37744698dup | CA2695225796 | HNF1B | c.188_191dup (p.Leu65TyrfsTer24)
| |
17 | g.37744695T>A | CA398753981 | HNF1B | c.190A>T (p.Thr64Ser)
| dbSNP gnomAD v3 gnomAD v4 |
17 | g.37744695T>C | CA398753987 | HNF1B | c.190A>G (p.Thr64Ala)
| |
17 | g.37744695T>G | CA398753990 | HNF1B | c.190A>C (p.Thr64Pro)
| |
17 | g.37744696A>C | CA398753994 | HNF1B | c.189T>G (p.His63Gln)
| |
17 | g.37744696A>G | CA499880146 | HNF1B | c.189T>C (p.His63=)
| |
17 | g.37744696A>T | CA398754000 | HNF1B | c.189T>A (p.His63Gln)
| |
17 | g.37744697T>A | CA398754004 | HNF1B | c.188A>T (p.His63Leu)
| |
17 | g.37744697T>C | CA398754007 | HNF1B | c.188A>G (p.His63Arg)
| |
17 | g.37744697T>G | CA398754010 | HNF1B | c.188A>C (p.His63Pro)
| gnomAD v4 |
17 | g.37744698G>A | CA8519135 | HNF1B | c.187C>T (p.His63Tyr)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.37744698G>C | CA398754015 | HNF1B | c.187C>G (p.His63Asp)
| |
17 | g.37744698G>T | CA398754019 | HNF1B | c.187C>A (p.His63Asn)
| |
17 | g.37744699del | CA1139665507 | HNF1B | c.187del (p.His63IlefsTer?)
| ClinVar dbSNP |
17 | g.37744699G>A | CA499880149 | HNF1B | c.186C>T (p.Phe62=)
| |
17 | g.37744699G>C | CA398754023 | HNF1B | c.186C>G (p.Phe62Leu)
| |
17 | g.37744699G>T | CA398754024 | HNF1B | c.186C>A (p.Phe62Leu)
| dbSNP |
17 | g.37744700A>C | CA8519136 | HNF1B | c.185T>G (p.Phe62Cys)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.37744700A>G | CA398754027 | HNF1B | c.185T>C (p.Phe62Ser)
| |
17 | g.37744700A>T | CA398754025 | HNF1B | c.185T>A (p.Phe62Tyr)
| dbSNP gnomAD v2 gnomAD v4 |
17 | g.37744701dup | CA2809374540 | HNF1B | c.185dup (p.His63ProfsTer25)
| |
17 | g.37744701A>C | CA398754040 | HNF1B | c.184T>G (p.Phe62Val)
| gnomAD v4 |
17 | g.37744701A>G | CA398754031 | HNF1B | c.184T>C (p.Phe62Leu)
| |
17 | g.37744701A>T | CA398754043 | HNF1B | c.184T>A (p.Phe62Ile)
| |
17 | g.37744702G>A | CA499880152 | HNF1B | c.183C>T (p.Val61=)
| gnomAD v4 |
17 | g.37744702G>C | CA499880154 | HNF1B | c.183C>G (p.Val61=)
| gnomAD v4 |
17 | g.37744702G>T | CA499880155 | HNF1B | c.183C>A (p.Val61=)
| gnomAD v4 |
17 | g.37744703A>C | CA8519137 | HNF1B | c.182T>G (p.Val61Gly)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37744703A>G | CA398754049 | HNF1B | c.182T>C (p.Val61Ala)
| |
17 | g.37744703A>T | CA398754053 | HNF1B | c.182T>A (p.Val61Asp)
| |
17 | g.37744704C>A | CA398754058 | HNF1B | c.181G>T (p.Val61Phe)
| |
17 | g.37744704C>G | CA398754062 | HNF1B | c.181G>C (p.Val61Leu)
| |
17 | g.37744704C>T | CA8519138 | HNF1B | c.181G>A (p.Val61Ile)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37744705C>A | CA499880158 | HNF1B | c.180G>T (p.Pro60=)
| |
17 | g.37744705C>G | CA499880159 | HNF1B | c.180G>C (p.Pro60=)
| |
17 | g.37744705C>T | CA499880160 | HNF1B | c.180G>A (p.Pro60=)
| |
17 | g.37744706G>A | CA8519140 | HNF1B | c.179C>T (p.Pro60Leu)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.37744706G>C | CA8519139 | HNF1B | c.179C>G (p.Pro60Arg)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37744706G>T | CA398754072 | HNF1B | c.179C>A (p.Pro60Gln)
| |
17 | g.37744707G>A | CA8519141 | HNF1B | c.178C>T (p.Pro60Ser)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37744707G>C | CA398754088 | HNF1B | c.178C>G (p.Pro60Ala)
| gnomAD v4 |
17 | g.37744707G>T | CA398754092 | HNF1B | c.178C>A (p.Pro60Thr)
| |
17 | g.37744708C>A | CA398754093 | HNF1B | c.177G>T (p.Lys59Asn)
| |
17 | g.37744708C>G | CA398754094 | HNF1B | c.177G>C (p.Lys59Asn)
| |
17 | g.37744708C>T | CA499880164 | HNF1B | c.177G>A (p.Lys59=)
| |
17 | g.37744709T>A | CA398754099 | HNF1B | c.176A>T (p.Lys59Met)
| |
17 | g.37744709T>C | CA398754095 | HNF1B | c.176A>G (p.Lys59Arg)
| |
17 | g.37744709T>G | CA398754096 | HNF1B | c.176A>C (p.Lys59Thr)
| |
17 | g.37744710T>A | CA398754102 | HNF1B | c.175A>T (p.Lys59Ter)
| |
17 | g.37744710T>C | CA398754106 | HNF1B | c.175A>G (p.Lys59Glu)
| |
17 | g.37744710T>G | CA398754107 | HNF1B | c.175A>C (p.Lys59Gln)
| |
17 | g.37744711G>A | CA8519142 | HNF1B | c.174C>T (p.Thr58=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37744711G>C | CA499880166 | HNF1B | c.174C>G (p.Thr58=)
| gnomAD v4 |
17 | g.37744711G>T | CA499880167 | HNF1B | c.174C>A (p.Thr58=)
| |
17 | g.37744712G>A | CA398754114 | HNF1B | c.173C>T (p.Thr58Ile)
| |
17 | g.37744712G>C | CA398754118 | HNF1B | c.173C>G (p.Thr58Ser)
| |
17 | g.37744712G>T | CA398754120 | HNF1B | c.173C>A (p.Thr58Asn)
| |
17 | g.37744713T>A | CA398754126 | HNF1B | c.172A>T (p.Thr58Ser)
| |
17 | g.37744713T>C | CA398754129 | HNF1B | c.172A>G (p.Thr58Ala)
| |
17 | g.37744713T>G | CA398754133 | HNF1B | c.172A>C (p.Thr58Pro)
| |
17 | g.37744714G>A | CA499880171 | HNF1B | c.171C>T (p.Asp57=)
| gnomAD v4 |
17 | g.37744714G>C | CA398754134 | HNF1B | c.171C>G (p.Asp57Glu)
| |
17 | g.37744714G>T | CA398754136 | HNF1B | c.171C>A (p.Asp57Glu)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37744715T>A | CA398754139 | HNF1B | c.170A>T (p.Asp57Val)
| |
17 | g.37744715T>C | CA398754141 | HNF1B | c.170A>G (p.Asp57Gly)
| |
17 | g.37744715T>G | CA398754140 | HNF1B | c.170A>C (p.Asp57Ala)
| |
17 | g.37744716C>A | CA398754143 | HNF1B | c.169G>T (p.Asp57Tyr)
| |
17 | g.37744716C>G | CA398754146 | HNF1B | c.169G>C (p.Asp57His)
| |
17 | g.37744716C>T | CA398754149 | HNF1B | c.169G>A (p.Asp57Asn)
| dbSNP |
17 | g.37744717G>A | CA499880178 | HNF1B | c.168C>T (p.Pro56=)
| ClinVar gnomAD v4 |
17 | g.37744717G>C | CA499880177 | HNF1B | c.168C>G (p.Pro56=)
| dbSNP gnomAD v2 gnomAD v4 |
17 | g.37744717G>T | CA499880176 | HNF1B | c.168C>A (p.Pro56=)
| |
17 | g.37744718G>A | CA398754154 | HNF1B | c.167C>T (p.Pro56Leu)
| |
17 | g.37744718G>C | CA398754157 | HNF1B | c.167C>G (p.Pro56Arg)
| |
17 | g.37744718G>T | CA398754159 | HNF1B | c.167C>A (p.Pro56His)
| |
17 | g.37744719G>A | CA398754161 | HNF1B | c.166C>T (p.Pro56Ser)
| |
17 | g.37744719G>C | CA398754163 | HNF1B | c.166C>G (p.Pro56Ala)
| |
17 | g.37744719G>T | CA398754164 | HNF1B | c.166C>A (p.Pro56Thr)
| |
17 | g.37744720C>A | CA398754165 | HNF1B | c.165G>T (p.Glu55Asp)
| |
17 | g.37744720C>G | CA398754166 | HNF1B | c.165G>C (p.Glu55Asp)
| |
17 | g.37744720C>T | CA499880183 | HNF1B | c.165G>A (p.Glu55=)
| gnomAD v4 |
17 | g.37744721T>A | CA398754171 | HNF1B | c.164A>T (p.Glu55Val)
| |
17 | g.37744721T>C | CA398754170 | HNF1B | c.164A>G (p.Glu55Gly)
| |
17 | g.37744721T>G | CA398754168 | HNF1B | c.164A>C (p.Glu55Ala)
| |
17 | g.37744722C>A | CA398754174 | HNF1B | c.163G>T (p.Glu55Ter)
| |
17 | g.37744722C>G | CA398754176 | HNF1B | c.163G>C (p.Glu55Gln)
| |
17 | g.37744722C>T | CA8519143 | HNF1B | c.163G>A (p.Glu55Lys)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37744723G>A | CA499880185 | HNF1B | c.162C>T (p.Ala54=)
| gnomAD v4 |
17 | g.37744723G>C | CA8519144 | HNF1B | c.162C>G (p.Ala54=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37744723G>T | CA499880186 | HNF1B | c.162C>A (p.Ala54=)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.37744724G>A | CA398754182 | HNF1B | c.161C>T (p.Ala54Val)
| gnomAD v4 |
17 | g.37744724G>C | CA398754184 | HNF1B | c.161C>G (p.Ala54Gly)
| |
17 | g.37744724G>T | CA398754186 | HNF1B | c.161C>A (p.Ala54Asp)
| |
17 | g.37744725C>A | CA398754191 | HNF1B | c.160G>T (p.Ala54Ser)
| |
17 | g.37744725C>G | CA8519145 | HNF1B | c.160G>C (p.Ala54Pro)
| dbSNP ExAC gnomAD v2 |
17 | g.37744725C>T | CA398754195 | HNF1B | c.160G>A (p.Ala54Thr)
| gnomAD v4 |
17 | g.37744728dup | CA2841364172 | HNF1B | c.160dup (p.Ala54GlyfsTer?)
| |
17 | g.37744728del | CA2841364173 | HNF1B | c.160del (p.Ala54ProfsTer?)
| |
17 | g.37744726C>A | CA499880190 | HNF1B | c.159G>T (p.Gly53=)
| |
17 | g.37744726C>G | CA499880191 | HNF1B | c.159G>C (p.Gly53=)
| |
17 | g.37744726C>T | CA499880192 | HNF1B | c.159G>A (p.Gly53=)
| dbSNP |
17 | g.37744727C>A | CA398754198 | HNF1B | c.158G>T (p.Gly53Val)
| |
17 | g.37744727C>G | CA398754201 | HNF1B | c.158G>C (p.Gly53Ala)
| |
17 | g.37744727C>T | CA398754204 | HNF1B | c.158G>A (p.Gly53Glu)
| |
17 | g.37744728C>A | CA398754211 | HNF1B | c.157G>T (p.Gly53Trp)
| ClinVar dbSNP |
17 | g.37744728C>G | CA398754220 | HNF1B | c.157G>C (p.Gly53Arg)
| |
17 | g.37744728C>T | CA398754209 | HNF1B | c.157G>A (p.Gly53Arg)
| ClinVar gnomAD v4 |
17 | g.37744729G>A | CA499880196 | HNF1B | c.156C>T (p.Ser52=)
| dbSNP gnomAD v2 gnomAD v4 |
17 | g.37744729G>C | CA398754232 | HNF1B | c.156C>G (p.Ser52Arg)
| dbSNP |
17 | g.37744729G>T | CA398754224 | HNF1B | c.156C>A (p.Ser52Arg)
| |
17 | g.37744730C>A | CA398754233 | HNF1B | c.155G>T (p.Ser52Ile)
| |
17 | g.37744730C>G | CA398754235 | HNF1B | c.155G>C (p.Ser52Thr)
| |
17 | g.37744730C>T | CA398754237 | HNF1B | c.155G>A (p.Ser52Asn)
| dbSNP gnomAD v2 gnomAD v4 |
17 | g.37744731T>A | CA398754240 | HNF1B | c.154A>T (p.Ser52Cys)
| |
17 | g.37744731T>C | CA398754241 | HNF1B | c.154A>G (p.Ser52Gly)
| |
17 | g.37744731T>G | CA398754242 | HNF1B | c.154A>C (p.Ser52Arg)
| ClinVar dbSNP |
17 | g.37744732G>A | CA499880025 | HNF1B | c.153C>T (p.Gly51=)
| gnomAD v4 |
17 | g.37744732G>C | CA499880024 | HNF1B | c.153C>G (p.Gly51=)
| |
17 | g.37744732G>T | CA499880023 | HNF1B | c.153C>A (p.Gly51=)
| |
17 | g.37744733C>A | CA398754243 | HNF1B | c.152G>T (p.Gly51Val)
| |
17 | g.37744733C>G | CA398754244 | HNF1B | c.152G>C (p.Gly51Ala)
| |
17 | g.37744733C>T | CA398754245 | HNF1B | c.152G>A (p.Gly51Asp)
| |
17 | g.37744734C>A | CA398754249 | HNF1B | c.151G>T (p.Gly51Cys)
| |
17 | g.37744734C>G | CA398754254 | HNF1B | c.151G>C (p.Gly51Arg)
| |
17 | g.37744734C>T | CA398754256 | HNF1B | c.151G>A (p.Gly51Ser)
| |
17 | g.37744734_37744735insCCTGTCCCCTGGCAGCGGGGCCG | CA2841364174 | HNF1B | c.150_151insCGGCCCCGCTGCCAGGGGACAGG (p.Gly51ArgfsTer?)
| |
17 | g.37744735A>C | CA499880028 | HNF1B | c.150T>G (p.Pro50=)
| ClinVar dbSNP gnomAD v4 |
17 | g.37744735A>G | CA499880029 | HNF1B | c.150T>C (p.Pro50=)
| |
17 | g.37744735A>T | CA499880030 | HNF1B | c.150T>A (p.Pro50=)
| |
17 | g.37744735_37744749del | CA2567235878 | HNF1B | c.136_150del (p.Leu46_Pro50del)
| |
17 | g.37744736G>A | CA398754263 | HNF1B | c.149C>T (p.Pro50Leu)
| |
17 | g.37744736G>C | CA398754258 | HNF1B | c.149C>G (p.Pro50Arg)
| |
17 | g.37744736G>T | CA398754261 | HNF1B | c.149C>A (p.Pro50His)
| |
17 | g.37744737G>A | CA8519146 | HNF1B | c.148C>T (p.Pro50Ser)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37744737G>C | CA398754270 | HNF1B | c.148C>G (p.Pro50Ala)
| dbSNP gnomAD v4 |
17 | g.37744737G>T | CA398754278 | HNF1B | c.148C>A (p.Pro50Thr)
| |
17 | g.37744738G>A | CA499880034 | HNF1B | c.147C>T (p.Ser49=)
| gnomAD v4 |
17 | g.37744738G>C | CA499880035 | HNF1B | c.147C>G (p.Ser49=)
| |
17 | g.37744738G>T | CA499880036 | HNF1B | c.147C>A (p.Ser49=)
| |
17 | g.37744739G>A | CA398754279 | HNF1B | c.146C>T (p.Ser49Phe)
| gnomAD v4 |
17 | g.37744739G>C | CA8519147 | HNF1B | c.146C>G (p.Ser49Cys)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.37744739G>T | CA398754281 | HNF1B | c.146C>A (p.Ser49Tyr)
| |
17 | g.37744740A>C | CA8519148 | HNF1B | c.145T>G (p.Ser49Ala)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.37744740A>G | CA398754282 | HNF1B | c.145T>C (p.Ser49Pro)
| |
17 | g.37744740A>T | CA290293210 | HNF1B | c.145T>A (p.Ser49Thr)
| dbSNP |
17 | g.37744741C>A | CA499880040 | HNF1B | c.144G>T (p.Leu48=)
| |
17 | g.37744741C>G | CA499880041 | HNF1B | c.144G>C (p.Leu48=)
| |
17 | g.37744741C>T | CA499880042 | HNF1B | c.144G>A (p.Leu48=)
| |
17 | g.37744742del | CA913190806 | HNF1B | c.143del (p.Leu48ArgfsTer?)
| ClinVar |
17 | g.37744742A>C | CA398754283 | HNF1B | c.143T>G (p.Leu48Arg)
| |
17 | g.37744742A>G | CA290293214 | HNF1B | c.143T>C (p.Leu48Pro)
| dbSNP gnomAD v4 |
17 | g.37744742A>T | CA398754284 | HNF1B | c.143T>A (p.Leu48Gln)
| |
17 | g.37744742_37744743del | CA2573332395 | HNF1B | c.142_143del (p.Leu48ValfsTer?)
| |
17 | g.37744743G>A | CA499880046 | HNF1B | c.142C>T (p.Leu48=)
| dbSNP gnomAD v3 gnomAD v4 |
17 | g.37744743G>C | CA398754287 | HNF1B | c.142C>G (p.Leu48Val)
| gnomAD v4 |
17 | g.37744743G>T | CA398754286 | HNF1B | c.142C>A (p.Leu48Met)
| |
17 | g.37744744G>A | CA499880047 | HNF1B | c.141C>T (p.Pro47=)
| dbSNP gnomAD v3 gnomAD v4 |
17 | g.37744744G>C | CA499880048 | HNF1B | c.141C>G (p.Pro47=)
| |
17 | g.37744744G>T | CA499880050 | HNF1B | c.141C>A (p.Pro47=)
| |
17 | g.37744745G>A | CA214348 | HNF1B | c.140C>T (p.Pro47Leu)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37744745G>C | CA398754294 | HNF1B | c.140C>G (p.Pro47Arg)
| |
17 | g.37744745G>T | CA398754288 | HNF1B | c.140C>A (p.Pro47His)
| gnomAD v4 |
17 | g.37744746G>A | CA8519150 | HNF1B | c.139C>T (p.Pro47Ser)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.37744746G>C | CA398754295 | HNF1B | c.139C>G (p.Pro47Ala)
| |
17 | g.37744746G>T | CA8519149 | HNF1B | c.139C>A (p.Pro47Thr)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.37744747C>A | CA499880051 | HNF1B | c.138G>T (p.Leu46=)
| |
17 | g.37744747C>G | CA499880053 | HNF1B | c.138G>C (p.Leu46=)
| |
17 | g.37744747C>T | CA499880054 | HNF1B | c.138G>A (p.Leu46=)
| gnomAD v4 |
17 | g.37744748A>C | CA398754297 | HNF1B | c.137T>G (p.Leu46Arg)
| dbSNP |
17 | g.37744748A>G | CA398754299 | HNF1B | c.137T>C (p.Leu46Pro)
| |
17 | g.37744748A>T | CA398754300 | HNF1B | c.137T>A (p.Leu46Gln)
| |
17 | g.37744749G>A | CA499880055 | HNF1B | c.136C>T (p.Leu46=)
| |
17 | g.37744749G>C | CA398754302 | HNF1B | c.136C>G (p.Leu46Val)
| |
17 | g.37744749G>T | CA398754305 | HNF1B | c.136C>A (p.Leu46Met)
| |
17 | g.37744750C>A | CA499880058 | HNF1B | c.135G>T (p.Thr45=)
| gnomAD v4 |
17 | g.37744750C>G | CA499880057 | HNF1B | c.135G>C (p.Thr45=)
| |
17 | g.37744750C>T | CA499880056 | HNF1B | c.135G>A (p.Thr45=)
| ClinVar dbSNP |
17 | g.37744750_37744751insCT | CA2559753703 | HNF1B | c.134_135insAG (p.Leu46GlyfsTer?)
| |
17 | g.37744751G>A | CA8519151 | HNF1B | c.134C>T (p.Thr45Met)
| dbSNP ExAC gnomAD v4 |
17 | g.37744751G>C | CA398754311 | HNF1B | c.134C>G (p.Thr45Arg)
| |
17 | g.37744751G>T | CA398754316 | HNF1B | c.134C>A (p.Thr45Lys)
| |
17 | g.37744752T>A | CA398754325 | HNF1B | c.133A>T (p.Thr45Ser)
| |
17 | g.37744752T>C | CA398754322 | HNF1B | c.133A>G (p.Thr45Ala)
| gnomAD v4 |
17 | g.37744752T>G | CA398754318 | HNF1B | c.133A>C (p.Thr45Pro)
| |
17 | g.37744753C>A | CA398754330 | HNF1B | c.132G>T (p.Glu44Asp)
| |
17 | g.37744753C>G | CA398754332 | HNF1B | c.132G>C (p.Glu44Asp)
| |
17 | g.37744753C>T | CA499880060 | HNF1B | c.132G>A (p.Glu44=)
| gnomAD v4 |
17 | g.37744754T>A | CA398754335 | HNF1B | c.131A>T (p.Glu44Val)
| |
17 | g.37744754T>C | CA398754339 | HNF1B | c.131A>G (p.Glu44Gly)
| |
17 | g.37744754T>G | CA398754345 | HNF1B | c.131A>C (p.Glu44Ala)
| |
17 | g.37744755C>A | CA398754348 | HNF1B | c.130G>T (p.Glu44Ter)
| |
17 | g.37744755C>G | CA398754349 | HNF1B | c.130G>C (p.Glu44Gln)
| ClinVar |
17 | g.37744755C>T | CA398754352 | HNF1B | c.130G>A (p.Glu44Lys)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37744756C>A | CA499880062 | HNF1B | c.129G>T (p.Leu43=)
| |
17 | g.37744756C>G | CA499880063 | HNF1B | c.129G>C (p.Leu43=)
| |
17 | g.37744756C>T | CA499880064 | HNF1B | c.129G>A (p.Leu43=)
| |
17 | g.37744757A>C | CA398754355 | HNF1B | c.128T>G (p.Leu43Arg)
| |
17 | g.37744757A>G | CA398754358 | HNF1B | c.128T>C (p.Leu43Pro)
| |
17 | g.37744757A>T | CA398754361 | HNF1B | c.128T>A (p.Leu43Gln)
| |
17 | g.37744758G>A | CA290293250 | HNF1B | c.127C>T (p.Leu43=)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.37744758G>C | CA8519152 | HNF1B | c.127C>G (p.Leu43Val)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37744758G>T | CA398754366 | HNF1B | c.127C>A (p.Leu43Met)
| |
17 | g.37744759C>A | CA398754370 | HNF1B | c.126G>T (p.Lys42Asn)
| |
17 | g.37744759C>G | CA398754375 | HNF1B | c.126G>C (p.Lys42Asn)
| |
17 | g.37744759C>T | CA499880068 | HNF1B | c.126G>A (p.Lys42=)
| |
17 | g.37744760T>A | CA398754378 | HNF1B | c.125A>T (p.Lys42Met)
| |
17 | g.37744760T>C | CA398754388 | HNF1B | c.125A>G (p.Lys42Arg)
| |
17 | g.37744760T>G | CA398754386 | HNF1B | c.125A>C (p.Lys42Thr)
| |
17 | g.37744761T>A | CA398754390 | HNF1B | c.124A>T (p.Lys42Ter)
| |
17 | g.37744761T>C | CA398754393 | HNF1B | c.124A>G (p.Lys42Glu)
| gnomAD v4 |
17 | g.37744761T>G | CA398754391 | HNF1B | c.124A>C (p.Lys42Gln)
| |
17 | g.37744762C>A | CA499880069 | HNF1B | c.123G>T (p.Val41=)
| |
17 | g.37744762C>G | CA499880070 | HNF1B | c.123G>C (p.Val41=)
| |
17 | g.37744762C>T | CA499880071 | HNF1B | c.123G>A (p.Val41=)
| |
17 | g.37744763A>C | CA398754394 | HNF1B | c.122T>G (p.Val41Gly)
| |
17 | g.37744763A>G | CA398754397 | HNF1B | c.122T>C (p.Val41Ala)
| |
17 | g.37744763A>T | CA398754408 | HNF1B | c.122T>A (p.Val41Glu)
| |
17 | g.37744764C>A | CA398754419 | HNF1B | c.121G>T (p.Val41Leu)
| |
17 | g.37744764C>G | CA398754422 | HNF1B | c.121G>C (p.Val41Leu)
| |
17 | g.37744764C>T | CA398754424 | HNF1B | c.121G>A (p.Val41Met)
| dbSNP gnomAD v2 gnomAD v4 |
17 | g.37744764_37744765insTC | CA2695225797 | HNF1B | c.121_122insAG (p.Val41GlufsTer2)
| |
17 | g.37744767del | CA658798822 | HNF1B | c.121del (p.Val41Ter)
| ClinVar dbSNP |