All variants in the KCNE1 gene

Information The variants shown are described using the NM_000219.4 transcript reference sequence.

117 entries on 2 pages. Showing entries 1 - 100.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Type     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Variant remarks     

ClassClinical     

Owner     
./. 02 c.-59-129T>C - - IVS2 - GenBank KCNE1_00059 0.41 SNP - Qi Ming
./. 02 c.-59-128G>A - - IVS2 - GenBank KCNE1_00060 0.02 SNP - Qi Ming
./. 02 c.-129C>T - - IVS2-129C>T - GenBank KCNE1_00066 0.42 SNP - Qi Ming
./. 02 c.-59-59T>C - - IVS2 - GenBank KCNE1_00061 0.01 SNP - Qi Ming
./. 00 c*124A>G - - C*124 A>G - GenBank KCNE1_00062 - SNP - Qi Ming
./. 00 c*124A>G - - C*124 A>G - GenBank KCNE1_00062 - SNP - Qi Ming
./. 00 c*132A>G - - C*132 A>G - GenBank KCNE1_00063 0.03 SNP - Qi Ming
./. 00 c*456C>T - - C*456 C>T - GenBank KCNE1_00064 0.50 SNP - Qi Ming
./. 00 c*456C>T - - C*456 C>T - GenBank KCNE1_00064 0.50 SNP - Qi Ming
./. 00 c*480G>C - - C*480 G>C - GenBank KCNE1_00065 0.05 SNP - Qi Ming
./. 03 c.13insT - p.Asn5XfsX1 - - GenBank KCNE1_00023 - Frame shift - Qi Ming
./. 03 c.152_153TG>AC - p.Leu51His no - GenBank KCNE1_00051 - Missense - Qi Ming
./. 03 c.9_12delGTCT - p.Leu3LeufsX6 - - GenBank KCNE1_00022 - Frame shift - Qi Ming
./. 03 c.20C>T - p.Thr7Ile C to T in nt 20 - GenBank KCNE1_00057 - Missense - Qi Ming
./. 03 c.23C>T - p.Ala8Val - - GenBank KCNE1_00024 - Missense - Qi Ming
./. 03 c.23C>T - p.Ala8Val 23C  T - GenBank KCNE1_00024 - Missense - Qi Ming
./. 03 c.29C>T - p.Thr10Met - - GenBank KCNE1_00025 - Missense - Qi Ming
./. 03 c.30G>A - p.Thr10Thr - - GenBank KCNE1_00005 - silent mutation - Qi Ming
./. 03 c.50G>A - p.Trp17X - - GenBank KCNE1_00026 - Nonsense - Qi Ming
./. 03 c.83C>T - p.Ser28Leu - - GenBank KCNE1_00027 - Missense - Qi Ming
./. 03 c.83C>T - p.Ser28Leu - - GenBank KCNE1_00027 - Missense - Qi Ming
./. 03 c.84G>A - p.Ser28Ser - - GenBank KCNE1_00003 - silent mutation - Qi Ming
./. 03 c.84G>A - p.Ser28Ser - - GenBank KCNE1_00003 - - - Qi Ming
./. 03 c.84G>A - p.Ser28Ser - - GenBank KCNE1_00003 0.021 - - Qi Ming
./. 03 c.84G>A - p.Ser28Ser G84A - GenBank KCNE1_00003 0.0052 silent mutation - Qi Ming
./. 03 c.84G>A - p.Ser28Ser C.84 G>A - GenBank KCNE1_00003 0.01 silent mutation - Qi Ming
./. 03 c.95G>A - p.Arg32His - - GenBank KCNE1_00009 N.D. Missense - Qi Ming
./. 03 c.95G>A - p.Arg32His - - GenBank KCNE1_00028 - Missense - Qi Ming
./. 03 c.95G>A - p.Arg32His - - GenBank KCNE1_00009 - Missense - Qi Ming
./. 03 c.95G>A - p.Arg32His 95G>A - GenBank KCNE1_00009 - Missense - Qi Ming
./. 03 c.107G>A - p.Arg36His - - GenBank KCNE1_00011 - Missense - Qi Ming
./. 03 c.112A>G - p.Ser38Gly Gly38Ser - GenBank KCNE1_00004 - Missense - Qi Ming
./. 03 c.112A>G - p.Ser38Gly Gly38Ser - GenBank KCNE1_00004 - Missense - Qi Ming
./. 03 c.112A>G - p.Ser38Gly - - GenBank KCNE1_00004 - Missense - Qi Ming
./. 03 c.112A>G - p.Ser38Gly Gly38Ser - GenBank KCNE1_00004 - Missense - Qi Ming
./. 03 c.112A>G - p.Ser38Gly Gly38Ser - GenBank KCNE1_00004 - Missense - Qi Ming
./. 03 c.112A>G - p.Ser38Gly - - GenBank KCNE1_00004 0.442 Missense - Qi Ming
./. 03 c.112A>G - p.Ser38Gly - - GenBank KCNE1_00004 0.441 Missense - Qi Ming
./. 03 c.112A>G - p.Ser38Gly G38S - GenBank KCNE1_00004 - Missense - Qi Ming
./. 03 c.112A>G - p.Ser38Gly no - GenBank KCNE1_00049 - Missense - Qi Ming
./. 03 c.112A>G - p.Ser38Gly - - GenBank KCNE1_00004 25/32 Missense - Qi Ming
./. 03 c.112A>G - p.Ser38Gly C.112 A>G - GenBank KCNE1_00004 0.38 Missense - Qi Ming
./. 03 c.112A>G - p.Ser38Gly no - GenBank KCNE1_00004 36.8% Missense - Qi Ming
./. 03 c.112A>G - p.Ser38Gly - - GenBank KCNE1_00004 - Missense - Qi Ming
./. 03 c.112G>A - p.Gly38Ser - - GenBank KCNE1_00013 36.1% polymorphism - Qi Ming
./. 03 c.112G>A - p.Gly38Ser - - GenBank KCNE1_00020 30% in normal - - Qi Ming
./. 03 c.112G>A - p.Gly38Ser - - GenBank KCNE1_00013 - Silent mutation - Qi Ming
./. 03 c.112G>A - p.Gly38Ser no - GenBank KCNE1_00053 54.2% Missense - Qi Ming
./. 03 c.112G>A - p.Gly38Ser - - GenBank KCNE1_00013 19% Missense - Qi Ming
./. 03 c.112G>A - p.Gly38Ser G112A - GenBank KCNE1_00013 0.24 Missense - Qi Ming
./. 03 c.112G>A - p.Gly38Ser 112G>A - GenBank KCNE1_00013 0.19 Missense - Qi Ming
./. 03 c.112G>A - p.Gly38Ser no - GenBank KCNE1_00055 3.3% Missense - Qi Ming
./. 03 c.112G>A - p.Gly38Ser no - GenBank KCNE1_00013 - Missense - Qi Ming
./. 03 c.112G>A - p.Gly38Ser 112G>A - GenBank KCNE1_00013 0.36-0.38 Missense - Qi Ming
./. 03 c.139G>T - p.Val47Phe no - GenBank KCNE1_00050 - Missense - Qi Ming
./. 03 c.154G>A - p.Gly52Arg - - GenBank KCNE1_00042 - Missense - Qi Ming
./. 03 c.155G>C - p.Gly52Ala - - GenBank KCNE1_00008 0.005 Missense - Qi Ming
./. 03 c.155G>C - p.Gly52Ala - - GenBank KCNE1_00014 0.3% Missense - Qi Ming
./. 03 c.158T>C - p.Phe53Ser - - GenBank KCNE1_00012 - Missense - Qi Ming
./. 03 c.159C>T - p.Phe53Phe C158T - GenBank KCNE1_00045 0.11 silent mutation. - Qi Ming
./. 03 c.162C>T - p.Phe54Phe - - GenBank KCNE1_00006 - silent mutation - Qi Ming
./. 03 c.162C>T - p.Phe54Phe - - GenBank KCNE1_00006 0.021 silent mutation - Qi Ming
./. 03 c.162C>T - p.Phe54Phe - - GenBank KCNE1_00021 2% in normal silent mutation - Qi Ming
./. 03 c.163G>A - p.Gly55Ser - - GenBank KCNE1_00029 - Missense - Qi Ming
./. 03 c.172A>C - p.Thr58Pro - - GenBank KCNE1_00030 - Missense - Qi Ming
./. 03 c.176T>C - p.Leu59Pro - - GenBank KCNE1_00031 - Missense - Qi Ming
./. 03 c.199C>T - P.Arg67Cys - - GenBank KCNE1_00032 - Missense - Qi Ming
./. 03 c.200G>A - p.Arg67His - - GenBank KCNE1_00033 - Missense - Qi Ming
./. 03 c.206A>G - p.Lys69Arg - - GenBank KCNE1_00015 0.3% Heterozygous frequency - Qi Ming
./. 03 c.209A>T - p.Lys70Met - - GenBank KCNE1_00034 - Missense - Qi Ming
./. 03 c.210G>C - p.Lys70Asn - - GenBank KCNE1_00018 - Missense - Qi Ming
./. 03 c.221C>T - p.Ser74Leu - - GenBank KCNE1_00044 - Missense - Qi Ming
./. 03 c.221C>T - p.Ser74Leu - - GenBank KCNE1_00044 - Missense - Qi Ming
./. 03 c.226G>A - p.Asp76Asn - - GenBank KCNE1_00035 - Missense - Qi Ming
./. 03 c.226G>A - p.Asp76Asn 254G>A - GenBank KCNE1_00041 - Missense - Qi Ming
./. 03 c.226G>A - p.Asp76Asn - - GenBank KCNE1_00035 - Missense - Qi Ming
./. 03 c.226G>A - p.Asp76Asn G to A in nt 266 - GenBank KCNE1_00035 - Missense - Qi Ming
./. 03 c.226G>A - p.Asp76Asn c.226G>A - GenBank KCNE1_00035 - Missense - Qi Ming
./. 03 c.226G>A - p.Asp76Asn no - GenBank KCNE1_00058 - Missense - Qi Ming
./. 03 c.227_229delACCinsTCTA - p.Asp76ValfsX35 - - GenBank KCNE1_00036 - Frame shift - Qi Ming
./. 03 c.240C>G - p.Val80Val - - GenBank KCNE1_00056 0.6% silent mutation - Qi Ming
./. 03 c.240C>T - p.Val80Val - - GenBank KCNE1_00046 0.021 silent mutation - Qi Ming
./. 03 c.242A>G - p.Tyr81Cys - - GenBank KCNE1_00019 - Missense - Qi Ming
./. 03 c.242A>G - p.Tyr81Cys - - GenBank KCNE1_00019 - Missense - Qi Ming
./. 03 c.247G>A - p.Glu83Lys - - GenBank KCNE1_00037 - Missense - Qi Ming
./. 03 c.253G>A - p.Asp85Asn - - GenBank KCNE1_00002 - Missense - Qi Ming
./. 03 c.253G>A - p.Asp85Asn - - GenBank KCNE1_00002 - Missense - Qi Ming
./. 03 c.253G>A - p.Asp85Asn - - GenBank KCNE1_00002 - Missense - Qi Ming
./. 03 c.253G>A - p.Asp85Asn - - GenBank KCNE1_00002 - Missense - Qi Ming
./. 03 c.253G>A - p.Asp85Asn - - GenBank KCNE1_00002 - Missense - Qi Ming
./. 03 c.253G>A - p.Asp85Asn - - GenBank KCNE1_00016 0.7% polymorphism - Qi Ming
./. 03 c.253G>A - p.Asp85Asn no - GenBank KCNE1_00048 - Missense - Qi Ming
./. 03 c.253G>A - p.Asp85Asn no - GenBank KCNE1_00054 0.8% Missense - Qi Ming
./. 03 c.253G>A - p.Asp85Asn - - GenBank KCNE1_00002 - Missense - Qi Ming
./. 03 c.253G>A - p.Asp85Asn - - GenBank KCNE1_00002 - Missense - Qi Ming
./. 03 c.253G>A - p.Asp85Asn - - GenBank KCNE1_00002 - Missense - Qi Ming
./. 03 c.253G>A - p.Asp85Asn - - GenBank KCNE1_00002 - Missense,Polymorphism - Qi Ming
./. 03 c.253G>A - p.Asp85Asn - - GenBank KCNE1_00002 - Missense,Ploymorphism - Qi Ming
./. 03 c.253G>A - p.Asp85Asn - - GenBank KCNE1_00002 - Missense, Polymorphism - Qi Ming
./. 03 c.253G>A - p.Asp85Asn G253A - GenBank KCNE1_00002 0.021 Missense - Qi Ming
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