Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.45645222A>C | CA359707059 | HCN1 | c.812T>G (p.Leu271Arg) n.40T>G | |
5 | g.45645222A>G | CA359707060 | HCN1 | c.812T>C (p.Leu271Pro) n.40T>C | |
5 | g.45645222A>T | CA359707061 | HCN1 | c.812T>A (p.Leu271His) n.40T>A | |
5 | g.45645223G>A | CA359707062 | HCN1 | c.811C>T (p.Leu271Phe) n.39C>T | |
5 | g.45645223G>C | CA359707063 | HCN1 | c.811C>G (p.Leu271Val) n.39C>G | |
5 | g.45645223G>T | CA359707064 | HCN1 | c.811C>A (p.Leu271Ile) n.39C>A | |
5 | g.45645224T>A | CA444260301 | HCN1 | c.810A>T (p.Arg270=) n.38A>T | |
5 | g.45645224T>C | CA444260303 | HCN1 | c.810A>G (p.Arg270=) n.38A>G | gnomAD v4 |
5 | g.45645224T>G | CA444260304 | HCN1 | c.810A>C (p.Arg270=) n.38A>C | |
5 | g.45645225C>A | CA359707065 | HCN1 | c.809G>T (p.Arg270Leu) n.37G>T | |
5 | g.45645225C>G | CA359707067 | HCN1 | c.809G>C (p.Arg270Pro) n.37G>C | |
5 | g.45645225C>T | CA359707066 | HCN1 | c.809G>A (p.Arg270Gln) n.37G>A | ClinVar dbSNP gnomAD v4 COSMIC |
5 | g.45645226G>A | CA3259415 | HCN1 | c.808C>T (p.Arg270Ter) n.36C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
5 | g.45645226G>C | CA359707068 | HCN1 | c.808C>G (p.Arg270Gly) n.36C>G | |
5 | g.45645226G= | CA1543790288 | HCN1 | c.808C= (p.Arg270=) n.36C= | |
5 | g.45645226G>T | CA444260310 | HCN1 | c.808C>A (p.Arg270=) n.36C>A | |
5 | g.45645227T>A | CA359707069 | HCN1 | c.807A>T (p.Leu269Phe) n.35A>T | |
5 | g.45645227T>C | CA444260314 | HCN1 | c.807A>G (p.Leu269=) n.35A>G | |
5 | g.45645227T>G | CA359707070 | HCN1 | c.807A>C (p.Leu269Phe) n.35A>C | |
5 | g.45645228A>C | CA359707073 | HCN1 | c.806T>G (p.Leu269Ter) n.34T>G | |
5 | g.45645228A>G | CA359707072 | HCN1 | c.806T>C (p.Leu269Ser) n.34T>C | |
5 | g.45645228A>T | CA359707071 | HCN1 | c.806T>A (p.Leu269Ter) n.34T>A | |
5 | g.45645229A>C | CA359707074 | HCN1 | c.805T>G (p.Leu269Val) n.33T>G | COSMIC |
5 | g.45645229A>G | CA444260321 | HCN1 | c.805T>C (p.Leu269=) n.33T>C | |
5 | g.45645229A>T | CA359707075 | HCN1 | c.805T>A (p.Leu269Ile) n.33T>A | |
5 | g.45645230T>A | CA359707076 | HCN1 | c.804A>T (p.Leu268Phe) n.32A>T | |
5 | g.45645230T>C | CA444260324 | HCN1 | c.804A>G (p.Leu268=) n.32A>G | dbSNP |
5 | g.45645230T>G | CA359707077 | HCN1 | c.804A>C (p.Leu268Phe) n.32A>C | |
5 | g.45645230T= | CA1543790295 | HCN1 | c.804A= (p.Leu268=) n.32A= | |
5 | g.45645231A>C | CA359707078 | HCN1 | c.803T>G (p.Leu268Ter) n.31T>G | |
5 | g.45645231A>G | CA359707079 | HCN1 | c.803T>C (p.Leu268Ser) n.31T>C | COSMIC |
5 | g.45645231A>T | CA359707080 | HCN1 | c.803T>A (p.Leu268Ter) n.31T>A | |
5 | g.45645233del | CA2578305117 | HCN1 | c.803del (p.Leu268TyrfsTer7) n.31del | |
5 | g.45645232A>C | CA359707081 | HCN1 | c.802T>G (p.Leu268Val) n.30T>G | |
5 | g.45645232A>G | CA444401523 | HCN1 | c.802T>C (p.Leu268=) n.30T>C | |
5 | g.45645232A>T | CA359707082 | HCN1 | c.802T>A (p.Leu268Ile) n.30T>A | |
5 | g.45645233A>C | CA444401524 | HCN1 | c.801T>G (p.Arg267=) n.29T>G | |
5 | g.45645233A>G | CA444401525 | HCN1 | c.801T>C (p.Arg267=) n.29T>C | gnomAD v4 |
5 | g.45645233A>T | CA444401526 | HCN1 | c.801T>A (p.Arg267=) n.29T>A | |
5 | g.45645234C>A | CA359707083 | HCN1 | c.800G>T (p.Arg267Leu) n.28G>T | COSMIC |
5 | g.45645234C= | CA1543790299 | HCN1 | c.800G= (p.Arg267=) n.28G= | |
5 | g.45645234C>G | CA359707084 | HCN1 | c.800G>C (p.Arg267Pro) n.28G>C | dbSNP |
5 | g.45645234C>T | CA118324606 | HCN1 | c.800G>A (p.Arg267His) n.28G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
5 | g.45645235G>A | CA359707085 | HCN1 | c.799C>T (p.Arg267Cys) n.27C>T | gnomAD v4 COSMIC |
5 | g.45645235G>C | CA359707086 | HCN1 | c.799C>G (p.Arg267Gly) n.27C>G | |
5 | g.45645235G>T | CA359707087 | HCN1 | c.799C>A (p.Arg267Ser) n.27C>A | |
5 | g.45645236C>A | CA359707089 | HCN1 | c.798G>T (p.Leu266Phe) n.26G>T | |
5 | g.45645236C>G | CA359707088 | HCN1 | c.798G>C (p.Leu266Phe) n.26G>C | |
5 | g.45645236C>T | CA444401533 | HCN1 | c.798G>A (p.Leu266=) n.26G>A | |
5 | g.45645237A>C | CA359707090 | HCN1 | c.797T>G (p.Leu266Trp) n.25T>G | |
5 | g.45645237A>G | CA359707091 | HCN1 | c.797T>C (p.Leu266Ser) n.25T>C | |
5 | g.45645237A>T | CA359707092 | HCN1 | c.797T>A (p.Leu266Ter) n.25T>A | |
5 | g.45645238A= | CA1543790303 | HCN1 | c.796T= (p.Leu266=) n.24T= | |
5 | g.45645238A>C | CA359707093 | HCN1 | c.796T>G (p.Leu266Val) n.24T>G | |
5 | g.45645238A>G | CA3259416 | HCN1 | c.796T>C (p.Leu266=) n.24T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.45645238A>T | CA359707094 | HCN1 | c.796T>A (p.Leu266Met) n.24T>A | |
5 | g.45645239G>A | CA444401537 | HCN1 | c.795C>T (p.Leu265=) n.23C>T | dbSNP gnomAD v2 gnomAD v4 |
5 | g.45645239G>C | CA444401539 | HCN1 | c.795C>G (p.Leu265=) n.23C>G | |
5 | g.45645239G= | CA1543790306 | HCN1 | c.795C= (p.Leu265=) n.23C= | |
5 | g.45645239G>T | CA3259417 | HCN1 | c.795C>A (p.Leu265=) n.23C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.45645243_45645248del | CA2673782208 | HCN1 | c.790_795del (p.Ser264_Leu265del) n.18_23del | gnomAD v4 |
5 | g.45645240A>C | CA359707095 | HCN1 | c.794T>G (p.Leu265Arg) n.22T>G | |
5 | g.45645240A>G | CA359707096 | HCN1 | c.794T>C (p.Leu265Pro) n.22T>C | |
5 | g.45645240A>T | CA359707097 | HCN1 | c.794T>A (p.Leu265His) n.22T>A | ClinVar |
5 | g.45645241G>A | CA359707098 | HCN1 | c.793C>T (p.Leu265Phe) n.21C>T | |
5 | g.45645241G>C | CA359707099 | HCN1 | c.793C>G (p.Leu265Val) n.21C>G | |
5 | g.45645241G= | CA1543790313 | HCN1 | c.793C= (p.Leu265=) n.21C= | |
5 | g.45645241G>T | CA359707100 | HCN1 | c.793C>A (p.Leu265Ile) n.21C>A | ClinVar dbSNP |
5 | g.45645242A>C | CA359707102 | HCN1 | c.792T>G (p.Ser264Arg) n.20T>G | |
5 | g.45645242A>G | CA444401542 | HCN1 | c.792T>C (p.Ser264=) n.20T>C | gnomAD v4 |
5 | g.45645242A>T | CA359707101 | HCN1 | c.792T>A (p.Ser264Arg) n.20T>A | |
5 | g.45645243C>A | CA359707103 | HCN1 | c.791G>T (p.Ser264Ile) n.19G>T | |
5 | g.45645243C>G | CA359707104 | HCN1 | c.791G>C (p.Ser264Thr) n.19G>C | |
5 | g.45645243C>T | CA359707105 | HCN1 | c.791G>A (p.Ser264Asn) n.19G>A | |
5 | g.45645244T>A | CA359707106 | HCN1 | c.790A>T (p.Ser264Cys) n.18A>T | ClinVar dbSNP |
5 | g.45645244T>C | CA3259418 | HCN1 | c.790A>G (p.Ser264Gly) n.18A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.45645244T>G | CA359707107 | HCN1 | c.790A>C (p.Ser264Arg) n.18A>C | |
5 | g.45645244T= | CA1543790322 | HCN1 | c.790A= (p.Ser264=) n.18A= | |
5 | g.45645245G>A | CA444401545 | HCN1 | c.789C>T (p.Leu263=) n.17C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.45645245G>C | CA444401546 | HCN1 | c.789C>G (p.Leu263=) n.17C>G | |
5 | g.45645245G= | CA1543790328 | HCN1 | c.789C= (p.Leu263=) n.17C= | |
5 | g.45645245G>T | CA444401548 | HCN1 | c.789C>A (p.Leu263=) n.17C>A | |
5 | g.45645246A>C | CA359707108 | HCN1 | c.788T>G (p.Leu263Arg) n.16T>G | |
5 | g.45645246A>G | CA359707109 | HCN1 | c.788T>C (p.Leu263Pro) n.16T>C | |
5 | g.45645246A>T | CA359707110 | HCN1 | c.788T>A (p.Leu263His) n.16T>A | |
5 | g.45645247G>A | CA359707111 | HCN1 | c.787C>T (p.Leu263Phe) n.15C>T | |
5 | g.45645247G>C | CA359707112 | HCN1 | c.787C>G (p.Leu263Val) n.15C>G | |
5 | g.45645247G>T | CA359707113 | HCN1 | c.787C>A (p.Leu263Ile) n.15C>A | COSMIC |
5 | g.45645248A>C | CA359707114 | HCN1 | c.786T>G (p.Ile262Met) n.14T>G | |
5 | g.45645248A>G | CA444401559 | HCN1 | c.786T>C (p.Ile262=) n.14T>C | |
5 | g.45645248A>T | CA444401560 | HCN1 | c.786T>A (p.Ile262=) n.14T>A | |
5 | g.45645249A>C | CA359707117 | HCN1 | c.785T>G (p.Ile262Ser) n.13T>G | |
5 | g.45645249A>G | CA359707116 | HCN1 | c.785T>C (p.Ile262Thr) n.13T>C | |
5 | g.45645249A>T | CA359707115 | HCN1 | c.785T>A (p.Ile262Asn) n.13T>A | |
5 | g.45645250T>A | CA359707118 | HCN1 | c.784A>T (p.Ile262Phe) n.12A>T | |
5 | g.45645250T>C | CA359707119 | HCN1 | c.784A>G (p.Ile262Val) n.12A>G | |
5 | g.45645250T>G | CA359707120 | HCN1 | c.784A>C (p.Ile262Leu) n.12A>C | |
5 | g.45645251T>A | CA359707121 | HCN1 | c.783A>T (p.Lys261Asn) n.11A>T | |
5 | g.45645251T>C | CA444401565 | HCN1 | c.783A>G (p.Lys261=) n.11A>G | |
5 | g.45645251T>G | CA359707122 | HCN1 | c.783A>C (p.Lys261Asn) n.11A>C | COSMIC |
5 | g.45645252T>A | CA359707123 | HCN1 | c.782A>T (p.Lys261Ile) n.10A>T | |
5 | g.45645252T>C | CA359707124 | HCN1 | c.782A>G (p.Lys261Arg) n.10A>G | |
5 | g.45645252T>G | CA359707125 | HCN1 | c.782A>C (p.Lys261Thr) n.10A>C | |
5 | g.45645253T>A | CA359707126 | HCN1 | c.781A>T (p.Lys261Ter) n.9A>T | |
5 | g.45645253T>C | CA359707127 | HCN1 | c.781A>G (p.Lys261Glu) n.9A>G | ClinVar dbSNP |
5 | g.45645253T>G | CA359707128 | HCN1 | c.781A>C (p.Lys261Gln) n.9A>C | |
5 | g.45645253T= | CA1543790333 | HCN1 | c.781A= (p.Lys261=) n.9A= | |
5 | g.45645254T>A | CA444401578 | HCN1 | c.780A>T (p.Thr260=) n.8A>T | |
5 | g.45645254T>C | CA444401576 | HCN1 | c.780A>G (p.Thr260=) n.8A>G | |
5 | g.45645254T>G | CA444401575 | HCN1 | c.780A>C (p.Thr260=) n.8A>C | |
5 | g.45645255G>A | CA359707129 | HCN1 | c.779C>T (p.Thr260Ile) n.7C>T | ClinVar |
5 | g.45645255G>C | CA359707130 | HCN1 | c.779C>G (p.Thr260Arg) n.7C>G | |
5 | g.45645255G>T | CA359707131 | HCN1 | c.779C>A (p.Thr260Lys) n.7C>A | |
5 | g.45645256T>A | CA359707133 | HCN1 | c.778A>T (p.Thr260Ser) n.6A>T | |
5 | g.45645256T>C | CA359707134 | HCN1 | c.778A>G (p.Thr260Ala) n.6A>G | |
5 | g.45645256T>G | CA359707132 | HCN1 | c.778A>C (p.Thr260Pro) n.6A>C | |
5 | g.45645257A>C | CA359707135 | HCN1 | c.777T>G (p.Phe259Leu) n.5T>G | |
5 | g.45645257A>G | CA444401583 | HCN1 | c.777T>C (p.Phe259=) n.5T>C | |
5 | g.45645257A>T | CA359707136 | HCN1 | c.777T>A (p.Phe259Leu) n.5T>A | |
5 | g.45645258A>C | CA359707137 | HCN1 | c.776T>G (p.Phe259Cys) n.4T>G | |
5 | g.45645258A>G | CA359707138 | HCN1 | c.776T>C (p.Phe259Ser) n.4T>C | |
5 | g.45645258A>T | CA359707139 | HCN1 | c.776T>A (p.Phe259Tyr) n.4T>A | |
5 | g.45645259A>C | CA359707140 | HCN1 | c.775T>G (p.Phe259Val) n.3T>G | |
5 | g.45645259A>G | CA359707141 | HCN1 | c.775T>C (p.Phe259Leu) n.3T>C | |
5 | g.45645259A>T | CA359707142 | HCN1 | c.775T>A (p.Phe259Ile) n.3T>A | |
5 | g.45645260C>A | CA359707143 | HCN1 | c.774G>T (p.Arg258Ser) n.2G>T | |
5 | g.45645260C>G | CA359707144 | HCN1 | c.774G>C (p.Arg258Ser) n.2G>C | COSMIC |
5 | g.45645260C>T | CA444401591 | HCN1 | c.774G>A (p.Arg258=) n.2G>A | gnomAD v4 |
5 | g.45645261C>A | CA359707145 | HCN1 | c.773G>T (p.Arg258Met) n.1G>T | |
5 | g.45645261C>G | CA359707146 | HCN1 | c.773G>C (p.Arg258Thr) n.1G>C | |
5 | g.45645261C>T | CA359707147 | HCN1 | c.773G>A (p.Arg258Lys) n.1G>A | |
5 | g.45645262T>A | CA359707148 | HCN1 | c.772A>T (p.Arg258Trp) | |
5 | g.45645262T>C | CA359707149 | HCN1 | c.772A>G (p.Arg258Gly) | |
5 | g.45645262T>G | CA444401594 | HCN1 | c.772A>C (p.Arg258=) | gnomAD v4 |
5 | g.45645263C>A | CA444401596 | HCN1 | c.771G>T (p.Val257=) | |
5 | g.45645263C>G | CA444401599 | HCN1 | c.771G>C (p.Val257=) | |
5 | g.45645263C>T | CA444401601 | HCN1 | c.771G>A (p.Val257=) | |
5 | g.45645264A>C | CA359707150 | HCN1 | c.770T>G (p.Val257Gly) | |
5 | g.45645264A>G | CA359707152 | HCN1 | c.770T>C (p.Val257Ala) | |
5 | g.45645264A>T | CA359707151 | HCN1 | c.770T>A (p.Val257Glu) | |
5 | g.45645265C>A | CA359707153 | HCN1 | c.769G>T (p.Val257Leu) | |
5 | g.45645265C>G | CA359707154 | HCN1 | c.769G>C (p.Val257Leu) | COSMIC |
5 | g.45645265C>T | CA359707155 | HCN1 | c.769G>A (p.Val257Met) | |
5 | g.45645266A>C | CA359707156 | HCN1 | c.768T>G (p.Ile256Met) | |
5 | g.45645266A>G | CA444401604 | HCN1 | c.768T>C (p.Ile256=) | |
5 | g.45645266A>T | CA444401607 | HCN1 | c.768T>A (p.Ile256=) | |
5 | g.45645267A>C | CA359707157 | HCN1 | c.767T>G (p.Ile256Ser) | |
5 | g.45645267A>G | CA359707158 | HCN1 | c.767T>C (p.Ile256Thr) | ClinVar |
5 | g.45645267A>T | CA359707159 | HCN1 | c.767T>A (p.Ile256Asn) | |
5 | g.45645268T>A | CA359707160 | HCN1 | c.766A>T (p.Ile256Phe) | |
5 | g.45645268T>C | CA359707161 | HCN1 | c.766A>G (p.Ile256Val) | |
5 | g.45645268T>G | CA359707162 | HCN1 | c.766A>C (p.Ile256Leu) | |
5 | g.45645269G>A | CA444401612 | HCN1 | c.765C>T (p.Arg255=) | dbSNP gnomAD v2 gnomAD v4 |
5 | g.45645269G>C | CA444401614 | HCN1 | c.765C>G (p.Arg255=) | |
5 | g.45645269G= | CA1543790339 | HCN1 | c.765C= (p.Arg255=) | |
5 | g.45645269G>T | CA444401616 | HCN1 | c.765C>A (p.Arg255=) | |
5 | g.45645270C>A | CA359707165 | HCN1 | c.764G>T (p.Arg255Leu) | |
5 | g.45645270C= | CA1543790342 | HCN1 | c.764G= (p.Arg255=) | |
5 | g.45645270C>G | CA359707164 | HCN1 | c.764G>C (p.Arg255Pro) | |
5 | g.45645270C>T | CA359707163 | HCN1 | c.764G>A (p.Arg255His) | dbSNP gnomAD v4 |
5 | g.45645271G>A | CA359707166 | HCN1 | c.763C>T (p.Arg255Cys) | ClinVar dbSNP COSMIC |
5 | g.45645271G>C | CA359707167 | HCN1 | c.763C>G (p.Arg255Gly) | |
5 | g.45645271G= | CA1543790348 | HCN1 | c.763C= (p.Arg255=) | |
5 | g.45645271G>T | CA359707168 | HCN1 | c.763C>A (p.Arg255Ser) | |
5 | g.45645272A>C | CA444401620 | HCN1 | c.762T>G (p.Leu254=) | |
5 | g.45645272A>G | CA444401622 | HCN1 | c.762T>C (p.Leu254=) | |
5 | g.45645272A>T | CA444401624 | HCN1 | c.762T>A (p.Leu254=) | |
5 | g.45645273A>C | CA359707169 | HCN1 | c.761T>G (p.Leu254Arg) | COSMIC |
5 | g.45645273A>G | CA359707170 | HCN1 | c.761T>C (p.Leu254Pro) | |
5 | g.45645273A>T | CA359707171 | HCN1 | c.761T>A (p.Leu254His) | |
5 | g.45645274G>A | CA359707172 | HCN1 | c.760C>T (p.Leu254Phe) | |
5 | g.45645274G>C | CA359707173 | HCN1 | c.760C>G (p.Leu254Val) | COSMIC |
5 | g.45645274G>T | CA359707174 | HCN1 | c.760C>A (p.Leu254Ile) | |
5 | g.45645275T>A | CA444401626 | HCN1 | c.759A>T (p.Ala253=) | |
5 | g.45645275T>C | CA444401627 | HCN1 | c.759A>G (p.Ala253=) | |
5 | g.45645275T>G | CA444401628 | HCN1 | c.759A>C (p.Ala253=) | |
5 | g.45645276G>A | CA359707175 | HCN1 | c.758C>T (p.Ala253Val) | |
5 | g.45645276G>C | CA359707176 | HCN1 | c.758C>G (p.Ala253Gly) | |
5 | g.45645276G>T | CA359707177 | HCN1 | c.758C>A (p.Ala253Glu) | |
5 | g.45645277C>A | CA359707180 | HCN1 | c.757G>T (p.Ala253Ser) | |
5 | g.45645277C>G | CA359707179 | HCN1 | c.757G>C (p.Ala253Pro) | |
5 | g.45645277C>T | CA359707178 | HCN1 | c.757G>A (p.Ala253Thr) | |
5 | g.45645278C>A | CA359707181 | HCN1 | c.756G>T (p.Arg252Ser) | |
5 | g.45645278C= | CA1543790352 | HCN1 | c.756G= (p.Arg252=) | |
5 | g.45645278C>G | CA359707182 | HCN1 | c.756G>C (p.Arg252Ser) | |
5 | g.45645278C>T | CA444401630 | HCN1 | c.756G>A (p.Arg252=) | dbSNP gnomAD v2 gnomAD v4 |
5 | g.45645279C>A | CA359707183 | HCN1 | c.755G>T (p.Arg252Met) | |
5 | g.45645279C>G | CA359707184 | HCN1 | c.755G>C (p.Arg252Thr) | |
5 | g.45645279C>T | CA359707185 | HCN1 | c.755G>A (p.Arg252Lys) | |
5 | g.45645280T>A | CA3259419 | HCN1 | c.754A>T (p.Arg252Trp) | dbSNP ExAC gnomAD v2 |
5 | g.45645280T>C | CA359707186 | HCN1 | c.754A>G (p.Arg252Gly) | |
5 | g.45645280T>G | CA444401634 | HCN1 | c.754A>C (p.Arg252=) | |
5 | g.45645280T= | CA1543790356 | HCN1 | c.754A= (p.Arg252=) | |
5 | g.45645281G>A | CA444401637 | HCN1 | c.753C>T (p.Ala251=) | |
5 | g.45645281G>C | CA444401636 | HCN1 | c.753C>G (p.Ala251=) | |
5 | g.45645281G>T | CA444401635 | HCN1 | c.753C>A (p.Ala251=) | |
5 | g.45645282G>A | CA359707187 | HCN1 | c.752C>T (p.Ala251Val) | |
5 | g.45645282G>C | CA359707188 | HCN1 | c.752C>G (p.Ala251Gly) | |
5 | g.45645282G>T | CA359707189 | HCN1 | c.752C>A (p.Ala251Asp) | |
5 | g.45645283C>A | CA359707190 | HCN1 | c.751G>T (p.Ala251Ser) | COSMIC |
5 | g.45645283C>G | CA359707191 | HCN1 | c.751G>C (p.Ala251Pro) | |
5 | g.45645283C>T | CA359707192 | HCN1 | c.751G>A (p.Ala251Thr) | |
5 | g.45645284T>A | CA444401639 | HCN1 | c.750A>T (p.Thr250=) | |
5 | g.45645284T>C | CA444401640 | HCN1 | c.750A>G (p.Thr250=) | dbSNP gnomAD v4 |
5 | g.45645284T>G | CA444401641 | HCN1 | c.750A>C (p.Thr250=) | |
5 | g.45645284T= | CA1543790359 | HCN1 | c.750A= (p.Thr250=) | |
5 | g.45645285G>A | CA359707194 | HCN1 | c.749C>T (p.Thr250Ile) | |
5 | g.45645285G>C | CA359707195 | HCN1 | c.749C>G (p.Thr250Arg) | dbSNP gnomAD v2 gnomAD v4 |
5 | g.45645285G= | CA1543790366 | HCN1 | c.749C= (p.Thr250=) | |
5 | g.45645285G>T | CA359707193 | HCN1 | c.749C>A (p.Thr250Lys) | |
5 | g.45645286T>A | CA359707198 | HCN1 | c.748A>T (p.Thr250Ser) | |
5 | g.45645286T>C | CA359707196 | HCN1 | c.748A>G (p.Thr250Ala) | |
5 | g.45645286T>G | CA359707197 | HCN1 | c.748A>C (p.Thr250Pro) | |
5 | g.45645287C>A | CA359707199 | HCN1 | c.747G>T (p.Lys249Asn) | |
5 | g.45645287C= | CA1543790370 | HCN1 | c.747G= (p.Lys249=) | |
5 | g.45645287C>G | CA359707200 | HCN1 | c.747G>C (p.Lys249Asn) | ClinVar |
5 | g.45645287C>T | CA3259420 | HCN1 | c.747G>A (p.Lys249=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.45645288T>A | CA359707201 | HCN1 | c.746A>T (p.Lys249Met) | |
5 | g.45645288T>C | CA359707202 | HCN1 | c.746A>G (p.Lys249Arg) | gnomAD v4 |
5 | g.45645288T>G | CA359707203 | HCN1 | c.746A>C (p.Lys249Thr) | |
5 | g.45645289T>A | CA359707204 | HCN1 | c.745A>T (p.Lys249Ter) | |
5 | g.45645289T>C | CA359707205 | HCN1 | c.745A>G (p.Lys249Glu) | |
5 | g.45645289T>G | CA359707206 | HCN1 | c.745A>C (p.Lys249Gln) | |
5 | g.45645290G>A | CA444401645 | HCN1 | c.744C>T (p.Tyr248=) | |
5 | g.45645290G>C | CA359707207 | HCN1 | c.744C>G (p.Tyr248Ter) | |
5 | g.45645290G>T | CA359707208 | HCN1 | c.744C>A (p.Tyr248Ter) | COSMIC |
5 | g.45645291T>A | CA359707211 | HCN1 | c.743A>T (p.Tyr248Phe) | COSMIC |
5 | g.45645291T>C | CA359707210 | HCN1 | c.743A>G (p.Tyr248Cys) | dbSNP |
5 | g.45645291T>G | CA359707209 | HCN1 | c.743A>C (p.Tyr248Ser) | |
5 | g.45645291T= | CA1543790377 | HCN1 | c.743A= (p.Tyr248=) | |
5 | g.45645292A>C | CA359707212 | HCN1 | c.742T>G (p.Tyr248Asp) | |
5 | g.45645292A>G | CA359707213 | HCN1 | c.742T>C (p.Tyr248His) | |
5 | g.45645292A>T | CA359707214 | HCN1 | c.742T>A (p.Tyr248Asn) | |
5 | g.45645293A>C | CA444401650 | HCN1 | c.741T>G (p.Val247=) | |
5 | g.45645293A>G | CA444401652 | HCN1 | c.741T>C (p.Val247=) | |
5 | g.45645293A>T | CA444401651 | HCN1 | c.741T>A (p.Val247=) | |
5 | g.45645294A>C | CA359707215 | HCN1 | c.740T>G (p.Val247Gly) | |
5 | g.45645294A>G | CA359707216 | HCN1 | c.740T>C (p.Val247Ala) | |
5 | g.45645294A>T | CA359707217 | HCN1 | c.740T>A (p.Val247Asp) | |
5 | g.45645295C>A | CA359707218 | HCN1 | c.739G>T (p.Val247Phe) | |
5 | g.45645295C>G | CA359707219 | HCN1 | c.739G>C (p.Val247Leu) | |
5 | g.45645295C>T | CA359707220 | HCN1 | c.739G>A (p.Val247Ile) | |
5 | g.45645296T>A | CA359707221 | HCN1 | c.738A>T (p.Glu246Asp) | |
5 | g.45645296T>C | CA444401658 | HCN1 | c.738A>G (p.Glu246=) | dbSNP |
5 | g.45645296T>G | CA359707222 | HCN1 | c.738A>C (p.Glu246Asp) | |
5 | g.45645297T>A | CA359707223 | HCN1 | c.737A>T (p.Glu246Val) | |
5 | g.45645297T>C | CA359707224 | HCN1 | c.737A>G (p.Glu246Gly) | |
5 | g.45645297T>G | CA359707225 | HCN1 | c.737A>C (p.Glu246Ala) | ClinVar dbSNP |
5 | g.45645298C>A | CA359707227 | HCN1 | c.736G>T (p.Glu246Ter) | COSMIC |
5 | g.45645298C>G | CA359707228 | HCN1 | c.736G>C (p.Glu246Gln) | |
5 | g.45645298C>T | CA359707226 | HCN1 | c.736G>A (p.Glu246Lys) | COSMIC |
5 | g.45645299A>C | CA444401662 | HCN1 | c.735T>G (p.Ser245=) | |
5 | g.45645299A>G | CA444401664 | HCN1 | c.735T>C (p.Ser245=) | |
5 | g.45645299A>T | CA444401665 | HCN1 | c.735T>A (p.Ser245=) | |
5 | g.45645300G>A | CA359707229 | HCN1 | c.734C>T (p.Ser245Phe) | ClinVar dbSNP gnomAD v4 |
5 | g.45645300G>C | CA359707230 | HCN1 | c.734C>G (p.Ser245Cys) | |
5 | g.45645300G= | CA1543790389 | HCN1 | c.734C= (p.Ser245=) | |
5 | g.45645300G>T | CA359707231 | HCN1 | c.734C>A (p.Ser245Tyr) | COSMIC |
5 | g.45645301A= | CA1543790393 | HCN1 | c.733T= (p.Ser245=) | |
5 | g.45645301A>C | CA359707232 | HCN1 | c.733T>G (p.Ser245Ala) | dbSNP gnomAD v2 gnomAD v4 |
5 | g.45645301A>G | CA359707233 | HCN1 | c.733T>C (p.Ser245Pro) | |
5 | g.45645301A>T | CA359707234 | HCN1 | c.733T>A (p.Ser245Thr) | |
5 | g.45645302A>C | CA359707235 | HCN1 | c.732T>G (p.Asp244Glu) | |
5 | g.45645302A>G | CA444401672 | HCN1 | c.732T>C (p.Asp244=) | |
5 | g.45645302A>T | CA359707236 | HCN1 | c.732T>A (p.Asp244Glu) | |
5 | g.45645303T>A | CA359707237 | HCN1 | c.731A>T (p.Asp244Val) | |
5 | g.45645303T>C | CA359707238 | HCN1 | c.731A>G (p.Asp244Gly) | ClinVar |
5 | g.45645303T>G | CA359707239 | HCN1 | c.731A>C (p.Asp244Ala) | |
5 | g.45645304C>A | CA359707242 | HCN1 | c.730G>T (p.Asp244Tyr) | |
5 | g.45645304C>G | CA359707241 | HCN1 | c.730G>C (p.Asp244His) | |
5 | g.45645304C>T | CA359707240 | HCN1 | c.730G>A (p.Asp244Asn) | COSMIC |
5 | g.45645305C>A | CA359707243 | HCN1 | c.729G>T (p.Met243Ile) | |
5 | g.45645305C>G | CA359707244 | HCN1 | c.729G>C (p.Met243Ile) | |
5 | g.45645305C>T | CA359707245 | HCN1 | c.729G>A (p.Met243Ile) | COSMIC |
5 | g.45645306A= | CA1543790394 | HCN1 | c.728T= (p.Met243=) | |
5 | g.45645306A>C | CA359707246 | HCN1 | c.728T>G (p.Met243Arg) | ClinVar dbSNP |
5 | g.45645306A>G | CA359707247 | HCN1 | c.728T>C (p.Met243Thr) | ClinVar |
5 | g.45645306A>T | CA359707248 | HCN1 | c.728T>A (p.Met243Lys) | |
5 | g.45645307T>A | CA359707249 | HCN1 | c.727A>T (p.Met243Leu) | |
5 | g.45645307T>C | CA359707250 | HCN1 | c.727A>G (p.Met243Val) | ClinVar dbSNP gnomAD v4 |
5 | g.45645307T>G | CA359707251 | HCN1 | c.727A>C (p.Met243Leu) | |
5 | g.45645307T= | CA1543790400 | HCN1 | c.727A= (p.Met243=) | |
5 | g.45645308T>A | CA444401679 | HCN1 | c.726A>T (p.Gly242=) | |
5 | g.45645308T>C | CA444401680 | HCN1 | c.726A>G (p.Gly242=) | |
5 | g.45645308T>G | CA3259421 | HCN1 | c.726A>C (p.Gly242=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.45645308T= | CA1543790414 | HCN1 | c.726A= (p.Gly242=) | |
5 | g.45645309C>A | CA359707252 | HCN1 | c.725G>T (p.Gly242Val) | |
5 | g.45645309C>G | CA359707253 | HCN1 | c.725G>C (p.Gly242Ala) | |
5 | g.45645309C>T | CA359707254 | HCN1 | c.725G>A (p.Gly242Glu) | gnomAD v4 |
5 | g.45645310C>A | CA359707257 | HCN1 | c.724G>T (p.Gly242Ter) | |
5 | g.45645310C>G | CA359707256 | HCN1 | c.724G>C (p.Gly242Arg) | |
5 | g.45645310C>T | CA359707255 | HCN1 | c.724G>A (p.Gly242Arg) | COSMIC |
5 | g.45645311T>A | CA359707258 | HCN1 | c.723A>T (p.Lys241Asn) | |
5 | g.45645311T>C | CA3259422 | HCN1 | c.723A>G (p.Lys241=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.45645311T>G | CA359707259 | HCN1 | c.723A>C (p.Lys241Asn) | COSMIC |
5 | g.45645311T= | CA1543790419 | HCN1 | c.723A= (p.Lys241=) | |
5 | g.45645312T>A | CA359707260 | HCN1 | c.722A>T (p.Lys241Ile) | |
5 | g.45645312T>C | CA359707261 | HCN1 | c.722A>G (p.Lys241Arg) | |
5 | g.45645312T>G | CA359707262 | HCN1 | c.722A>C (p.Lys241Thr) | |
5 | g.45645313T>A | CA359707263 | HCN1 | c.721A>T (p.Lys241Ter) | ClinVar |
5 | g.45645313T>C | CA359707264 | HCN1 | c.721A>G (p.Lys241Glu) | gnomAD v4 |
5 | g.45645313T>G | CA359707265 | HCN1 | c.721A>C (p.Lys241Gln) | |
5 | g.45645314T>A | CA359707267 | HCN1 | c.720A>T (p.Glu240Asp) | ClinVar dbSNP |
5 | g.45645314T>C | CA444401690 | HCN1 | c.720A>G (p.Glu240=) | dbSNP |
5 | g.45645314T>G | CA359707266 | HCN1 | c.720A>C (p.Glu240Asp) | dbSNP |
5 | g.45645314T= | CA1543790427 | HCN1 | c.720A= (p.Glu240=) | |
5 | g.45645315T>A | CA359707268 | HCN1 | c.719A>T (p.Glu240Val) | |
5 | g.45645315T>C | CA359707269 | HCN1 | c.719A>G (p.Glu240Gly) | ClinVar dbSNP |
5 | g.45645315T>G | CA359707270 | HCN1 | c.719A>C (p.Glu240Ala) | |
5 | g.45645316C>A | CA359707271 | HCN1 | c.718G>T (p.Glu240Ter) | |
5 | g.45645316C>G | CA359707272 | HCN1 | c.718G>C (p.Glu240Gln) | |
5 | g.45645316C>T | CA359707273 | HCN1 | c.718G>A (p.Glu240Lys) | COSMIC |
5 | g.45645317T>A | CA444401692 | HCN1 | c.717A>T (p.Val239=) | |
5 | g.45645317T>C | CA444401693 | HCN1 | c.717A>G (p.Val239=) | dbSNP gnomAD v2 gnomAD v4 |
5 | g.45645317T>G | CA444401694 | HCN1 | c.717A>C (p.Val239=) | |
5 | g.45645317T= | CA1543790434 | HCN1 | c.717A= (p.Val239=) | |
5 | g.45645318A>C | CA359707274 | HCN1 | c.716T>G (p.Val239Gly) | |
5 | g.45645318A>G | CA359707276 | HCN1 | c.716T>C (p.Val239Ala) | |
5 | g.45645318A>T | CA359707275 | HCN1 | c.716T>A (p.Val239Glu) | |
5 | g.45645319C>A | CA359707277 | HCN1 | c.715G>T (p.Val239Leu) | |
5 | g.45645319C>G | CA359707278 | HCN1 | c.715G>C (p.Val239Leu) | |
5 | g.45645319C>T | CA359707279 | HCN1 | c.715G>A (p.Val239Ile) | |
5 | g.45645320A>C | CA359707280 | HCN1 | c.714T>G (p.Ile238Met) | |
5 | g.45645320A>G | CA444401697 | HCN1 | c.714T>C (p.Ile238=) | gnomAD v4 |
5 | g.45645320A>T | CA444401698 | HCN1 | c.714T>A (p.Ile238=) | |
5 | g.45645321A= | CA1543790439 | HCN1 | c.713T= (p.Ile238=) | |
5 | g.45645321A>C | CA359707281 | HCN1 | c.713T>G (p.Ile238Ser) | |
5 | g.45645321A>G | CA359707282 | HCN1 | c.713T>C (p.Ile238Thr) | |
5 | g.45645321A>T | CA359707283 | HCN1 | c.713T>A (p.Ile238Asn) | dbSNP |
5 | g.45645322T>A | CA359707284 | HCN1 | c.712A>T (p.Ile238Phe) | |
5 | g.45645322T>C | CA359707285 | HCN1 | c.712A>G (p.Ile238Val) | |
5 | g.45645322T>G | CA359707286 | HCN1 | c.712A>C (p.Ile238Leu) | dbSNP |
5 | g.45645322T= | CA1543790446 | HCN1 | c.712A= (p.Ile238=) |