All variants in the KCNQ1 gene

Information The variants shown are described using the NM_000218.2 transcript reference sequence.

961 entries on 10 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     
./. 00 c.-129C>T - - 5' UTR - GenBank KCNQ1_00450 0.7% SNP - Qi Ming
./. 01 c.-5T>C - - 5' UTR - GenBank KCNQ1_00060 - - - Qi Ming
./. 08 c.1071G>? - p.Gln357His Exon - GenBank KCNQ1_00546 - Missense - Qi Ming
./. 08 c.1124_1127TTCA - p.Ile375ArgfsX43 Exon - GenBank KCNQ1_00534 - frame shift, splice site - Qi Ming
./. 09 c.1135? - p.Trp379Ser Exon - GenBank KCNQ1_00547 - Missense - Qi Ming
./. 10 c.1258insA - p.Phe420fsX42 Exon - GenBank KCNQ1_00460 - frame shift - Qi Ming
./. 10 c.1338insC - p.Asp446fsX16 Exon - GenBank KCNQ1_00467 - frame shift - Qi Ming
./. 13 c.1684_1685delAG+1delG - p. Exon - GenBank KCNQ1_00501 - frame shift and splice site - Qi Ming
./. 01 c.386+81insGG - - Intron - GenBank KCNQ1_00448 3.9% Insertion - Qi Ming
./. 02 c.477+80insGG - - Intron - GenBank KCNQ1_00564 0.31 SNP - Qi Ming
./. 03 c.484_486? - p.Val162fsX72 Exon - GenBank KCNQ1_00512 - frame shift - Qi Ming
./. 03 c.567insG - p.Arg190AlafsX95 Exon - GenBank KCNQ1_00503 - frame shift - Qi Ming
./. 03 c.567insG - p.Arg190AlafsX95 Exon - GenBank KCNQ1_00503 - frame shift - Qi Ming
./. 05 c.743_744GG>TC - p.Trp248Phe Exon - GenBank KCNQ1_00441 - Missense - Qi Ming
./. 05 c.744G>? - p.Trp248Cys Exon - GenBank KCNQ1_00500 - Missense - Qi Ming
./. 07 c.938_939TC>AA - p.Ile313Lys Exon - GenBank KCNQ1_00480 - Missense - Qi Ming
./. 01 c.5C>T - p.Ala2Val Exon - GenBank KCNQ1_00230 - Missense - Qi Ming
./. 01 c.19C>T - p.Pro7Ser Exon - GenBank KCNQ1_00231 - Missense mutation - Qi Ming
./. 01 c.33G>A - p.Glu11Glu Exon - GenBank KCNQ1_00103 - SNP N.D. - Qi Ming
./. 01 c.39G>A - p.Lys13Lys Exon - GenBank KCNQ1_00510 - SNP N.D. - Qi Ming
./. 01 c.40C>T - p.Arg14Cys Exon - GenBank KCNQ1_00474 - Missense - Qi Ming
./. 01 c.107_108insT - p.Phe36PhefsX248 Exon - GenBank KCNQ1_00232 - Frame shift - Qi Ming
./. 01 c.117G>A - p.Glu39Glu Exon - GenBank KCNQ1_00105 - silent mutation - Qi Ming
./. 01 c.136G>A - p.Ala46Thr Exon - GenBank KCNQ1_00181 - Missense - Qi Ming
./. 01 c.136G>A - p.Ala46Thr Exon - GenBank KCNQ1_00233 - Missense mutation - Qi Ming
./. 01 c.136G>A - p.Ala46Thr Exon - GenBank KCNQ1_00181 - Missense - Qi Ming
./. 01 c.151_152insT - p.Tyr51LeufsX234 Exon - GenBank KCNQ1_00182 - frame shift insertion - Qi Ming
./. 01 c.153C>G - p.Tyr51X Exon - GenBank KCNQ1_00234 - Nonsense mutation - Qi Ming
./. 01 c.153C>G - p.Tyr51X Exon - GenBank KCNQ1_00234 - Nonsense - Qi Ming
./. 01 c.160_168dupATCGCGCCC - p.Ile54_Pro56dup Exon - GenBank KCNQ1_00137 - in-frame duplication - Qi Ming
./. 01 c.160_168dupATCGCGCCC - p.Ile54_Pro56dup Exon - GenBank KCNQ1_00192 - in-frame duplication - Qi Ming
./. 01 c.160_168dupATCGCGCCC - p.p.Ile54_Pro56dup Exon - GenBank KCNQ1_00137 - in-frame duplication - Qi Ming
./. 01 c.174G>A - p.Thr58Thr Exon - GenBank KCNQ1_00449 1.06% silent mutation - Qi Ming
./. 01 c.176delC - p.Pro59ProfsX27 Exon - GenBank KCNQ1_00235 - Frame shift - Qi Ming
./. 01 c.190_210delCCTGCGTCCCCGGCCGCGCCC - p.Pro64_Pro70del Exon - GenBank KCNQ1_00236 - In-frame deletion - Qi Ming
./. 01 c.191C>A - p.Pro64His Exon - GenBank KCNQ1_00106 - SNP N.D. - Qi Ming
./. 01 c.194C>T - p.Ala65Val Exon - GenBank KCNQ1_00107 - SNP N.D. - Qi Ming
./. 01 c.197C>T - p.Ser66Phe Exon - GenBank KCNQ1_00237 - Missense mutation - Qi Ming
./. 01 c.200_210delCGGCCGCGCCC - p.Pro67ArgfsX214 Exon - GenBank KCNQ1_00238 - Frame shift - Qi Ming
./. 01 c.211_219delGCCGCGCCC - p.Ala71_Pro73del Exon - GenBank KCNQ1_00459 - in-frame deletion - Qi Ming
./. 01 c.211_219delGCCGCGCCC - p.Ala71_Pro73del Exon - GenBank KCNQ1_00476 - In-frame deletion - Qi Ming
./. 01 c.211_219delGCCGCGCCC - p.Ala71_Pro73del Exon - GenBank KCNQ1_00459 - in-frame deletion - Qi Ming
./. 01 c.211_219delGCCGCGCCC - p.Ala71_Pro73del Exon - GenBank KCNQ1_00459 - in-frame deletion - Qi Ming
./. 01 c.217C>A - p.Pro73Thr Exon - GenBank KCNQ1_00239 - Missense mutation - Qi Ming
./. 01 c.217C>A - p.Pro73Thr Exon - GenBank KCNQ1_00239 - Missense - Qi Ming
./. 01 c.228C>T - p.Ala76Ala Exon - GenBank KCNQ1_00108 - SNP N.D. - Qi Ming
./. 01 c.242_264delCGCGGCCGCCGGTGAGCCTAGACinsGCGCCCGCGG - p.Pro81ArgfsX152 Exon - GenBank KCNQ1_00240 - Frame shift - Qi Ming
./. 01 c.273_299delCTCCATCTACAGCACGCGCCGCCCGGTinsGG - p.Val91ValfsX138 Exon - GenBank KCNQ1_00241 - Frame shift - Qi Ming
./. 01 c.279C>A - p.Ile93Ile Exon - GenBank KCNQ1_00109 - SNP N.D. - Qi Ming
./. 01 c.287delC - p.Thr96SerfsX141 Exon - GenBank KCNQ1_00516 - frame shift deletion - Qi Ming
./. 01 c.309C>A - p.Arg103Arg Exon - GenBank KCNQ1_00110 - SNP N.D. - Qi Ming
./. 01 c.313delC - p.His105Thrfs*132 Exon - GenBank KCNQ1_00590 - - - Qi Ming
./. 01 c.313delC - p.His105Thrfs*132 Exon - GenBank KCNQ1_00590 - - - Qi Ming
./. 01 c.328G>A - p.Val110Ile Exon - GenBank KCNQ1_00413 - Missense - Qi Ming
./. 01 c.332A>G - p.Tyr111Cys Exon - GenBank KCNQ1_00242 - Missense mutation - Qi Ming
./. 01 c.341T>C - p.Leu114Pro Exon - GenBank KCNQ1_00055 - Missense - Qi Ming
./. 01 c.344A>G - p.Glu115Gly Exon - GenBank KCNQ1_00517 - Missense - Qi Ming
./. 01 c.350C>T - p.Pro117Leu Exon - GenBank KCNQ1_00243 - Missense mutation - Qi Ming
./. 01 c.354C>T - p.Thr118Thr Exon - GenBank KCNQ1_00096 - Silent mutation - Qi Ming
./. 01 c.356G>A - p.Gly119Asp Exon - GenBank KCNQ1_00096 0.004 Missense - Qi Ming
./. 01 c.357C>A - p.Gly119Gly Exon - GenBank KCNQ1_00111 - SNP N.D. - Qi Ming
./. 01 c.358_359insG - p.Trp120TrpfsX165 Exon - GenBank KCNQ1_00112 - SNP N.D. - Qi Ming
./. 01 c.360_361insA - p.Lys121LysfsX164 Exon - GenBank KCNQ1_00573 - frame shift insertion - Qi Ming
./. 01 c.364_365insT - p.Cys122LeufsX163 Exon - GenBank KCNQ1_00244 - Frame shift - Qi Ming
./. 01 c.365G>A - p.Cys122Tyr Exon - GenBank KCNQ1_00519 - Missense - Qi Ming
./. 01 c.365_366insG - p.Cys122TrpfsX629 Exon - GenBank KCNQ1_00518 - frame shift - Qi Ming
./. 01 c.381C>A - p.Phe127Leu Exon - GenBank KCNQ1_00280 - Missense - Qi Ming
./. 01 c.385G>A - p.Val129Ile Exon - GenBank KCNQ1_00193 0.3% Heterozygous frequency - Qi Ming
./. 01 c.386+1G>A - - Intron - GenBank KCNQ1_00245 - Splice site - Qi Ming
./. 01 c.386+5G>A - - Intron - GenBank KCNQ1_00445 - Splice site - Qi Ming
./. 01 c.386+9C>A - - Intron - GenBank KCNQ1_00094 - SNP - Qi Ming
./. 01 c.386+9C>G - - Intron - GenBank KCNQ1_00485 - SNP - Qi Ming
./. 02 c.387-5T>A - - Intron - GenBank KCNQ1_00071 - splice site - Qi Ming
./. 02 c.387-5T>A - - Intron - GenBank KCNQ1_00071 - splice site - Qi Ming
./. 02 c.397G>A - p.Val133Ile Exon - GenBank KCNQ1_00246 - Missense mutation - Qi Ming
./. 02 c.397G>A - p.Val133Ile Exon - GenBank KCNQ1_00246 - Missense - Qi Ming
./. 02 c.397G>A - p.Val133Ile Exon - GenBank KCNQ1_00246 - Missense - Qi Ming
./. 02 c.401T>C - p.Leu134Pro Exon - GenBank KCNQ1_00247 - Missense mutation - Qi Ming
./. 02 c.403delG - p.Val135SerfsX102 Exon - GenBank KCNQ1_00248 - Frame shift - Qi Ming
./. 02 c.407G>T - p.Cys136Phe Exon - GenBank KCNQ1_00520 - Missense - Qi Ming
./. 02 c.409C>T - p.Leu137Phe Exon - GenBank KCNQ1_00151 - Missense - Qi Ming
./. 02 c.418A>G - p.Ser140Gly Exon - GenBank KCNQ1_00076 - Missense mutation - Qi Ming
./. 02 c.418A>G - p.Ser140Gly Exon - GenBank KCNQ1_00076 - Missense - Qi Ming
./. 02 c.418A>G - p.Ser140Gly Exon - GenBank KCNQ1_00076 - Missense - Qi Ming
./. 02 c.420C>A - p.Ser140Arg Exon - GenBank KCNQ1_00591 - - - Qi Ming
./. 02 c.421G>A - p.Val141Met Exon - GenBank KCNQ1_00442 - Missense - Qi Ming
./. 02 c.421G>A - p.Val141Met Exon - GenBank KCNQ1_00442 - Missense - Qi Ming
./. 02 c.430A>G - p.Thr144Ala Exon - GenBank KCNQ1_00249 - Missense mutation - Qi Ming
./. 02 c.430A>G - p.Thr144Ala Exon - GenBank KCNQ1_00102 - Missense - Qi Ming
./. 02 c.430A>G - p.Thr144Ala Exon - GenBank KCNQ1_00102 - Missense - Qi Ming
./. 02 c.435C>T - p.Ile145Ile Exon - GenBank KCNQ1_00010 - silent mutation - Qi Ming
./. 02 c.435C>T - p.Ile145Ile Exon - GenBank KCNQ1_00010 - silent mutation - Qi Ming
./. 02 c.435C>T - p.Ile145Ile Exon - GenBank KCNQ1_00010 - silent mutation - Qi Ming
./. 02 c.435C>T - p.Ile145Ile Exon - GenBank KCNQ1_00010 - silent mutation - Qi Ming
./. 02 c.435C>T - p.Ile145Ile Exon - GenBank KCNQ1_00010 - silent mutation - Qi Ming
./. 02 c.435C>T - p.Ile145Ile Exon - GenBank KCNQ1_00010 - SNP 0.006 - Qi Ming
./. 02 c.435C>T - p.Ile145Ile Exon - GenBank KCNQ1_00010 - SNP N.D. - Qi Ming
./. 02 c.435C>T - p.Ile145Ile Exon - GenBank KCNQ1_00220 22% in normal polymorphism - Qi Ming
./. 02 c.435C>T - p.Ile145Ile Exon - GenBank KCNQ1_00010 - silent mutation - Qi Ming
./. 02 c.435C>T - p.Ile145Ile Exon - GenBank KCNQ1_00010 0.06 silent mutation - Qi Ming
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