Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.150958420_150958453delCA2695208647KCNH2n.1358_1391del
c.525_558del (p.Arg176AlafsTer14)
c.235-58_235-25del (n.235-58_235-25del)
n.748_781del
c.225_258del (p.Arg76AlafsTer14)
c.375_408del (p.Arg126AlafsTer14)
c.348_381del (p.Arg117AlafsTer14)
7g.150958423_150958435delCA2499218814KCNH2n.1377_1389del
c.544_556del (p.Ser182AlafsTer15)
c.235-39_235-27del (n.235-39_235-27del)
n.767_779del
c.244_256del (p.Ser82AlafsTer15)
c.394_406del (p.Ser132AlafsTer15)
c.367_379del (p.Ser123AlafsTer15)
ClinVar dbSNP
7g.150958428_150958435dupCA658797049KCNH2n.1377_1384dup
c.544_551dup (p.Ala185ArgfsTer19)
c.235-39_235-32dup (n.235-39_235-32dup)
n.767_774dup
c.244_251dup (p.Ala85ArgfsTer19)
c.394_401dup (p.Ala135ArgfsTer19)
c.367_374dup (p.Ala126ArgfsTer19)
ClinVar dbSNP
7g.150958431_150958438dupCA658797050KCNH2n.1370_1377dup
c.537_544dup (p.Ser182TrpfsTer22)
c.235-46_235-39dup (n.235-46_235-39dup)
n.760_767dup
c.237_244dup (p.Ser82TrpfsTer22)
c.387_394dup (p.Ser132TrpfsTer22)
c.360_367dup (p.Ser123TrpfsTer22)
ClinVar dbSNP
7g.150958434G>ACA369863375KCNH2n.1374C>T
c.541C>T (p.Arg181Trp)
c.235-42C>T (n.235-42C>T)
n.764C>T
c.241C>T (p.Arg81Trp)
c.391C>T (p.Arg131Trp)
c.364C>T (p.Arg122Trp)
dbSNP gnomAD v2 gnomAD v4
7g.150958434G>CCA369863376KCNH2n.1374C>G
c.541C>G (p.Arg181Gly)
c.235-42C>G (n.235-42C>G)
n.764C>G
c.241C>G (p.Arg81Gly)
c.391C>G (p.Arg131Gly)
c.364C>G (p.Arg122Gly)
gnomAD v4
7g.150958434G=CA1752418700KCNH2n.1374C=
c.541C= (p.Arg181=)
c.235-42C= (n.235-42C=)
n.764C=
c.241C= (p.Arg81=)
c.391C= (p.Arg131=)
c.364C= (p.Arg122=)
7g.150958434G>TCA458646816KCNH2n.1374C>A
c.541C>A (p.Arg181=)
c.235-42C>A (n.235-42C>A)
n.764C>A
c.241C>A (p.Arg81=)
c.391C>A (p.Arg131=)
c.364C>A (p.Arg122=)
gnomAD v4
7g.150958435C>ACA458646817KCNH2n.1373G>T
c.540G>T (p.Val180=)
c.235-43G>T (n.235-43G>T)
n.763G>T
c.240G>T (p.Val80=)
c.390G>T (p.Val130=)
c.363G>T (p.Val121=)
gnomAD v4
7g.150958435C=CA1752418702KCNH2n.1373G=
c.540G= (p.Val180=)
c.235-43G= (n.235-43G=)
n.763G=
c.240G= (p.Val80=)
c.390G= (p.Val130=)
c.363G= (p.Val121=)
7g.150958435C>GCA458646819KCNH2n.1373G>C
c.540G>C (p.Val180=)
c.235-43G>C (n.235-43G>C)
n.763G>C
c.240G>C (p.Val80=)
c.390G>C (p.Val130=)
c.363G>C (p.Val121=)
7g.150958435C>TCA458646818KCNH2n.1373G>A
c.540G>A (p.Val180=)
c.235-43G>A (n.235-43G>A)
n.763G>A
c.240G>A (p.Val80=)
c.390G>A (p.Val130=)
c.363G>A (p.Val121=)
ClinVar dbSNP gnomAD v4
7g.150958436A>CCA369863378KCNH2n.1372T>G
c.539T>G (p.Val180Gly)
c.235-44T>G (n.235-44T>G)
n.762T>G
c.239T>G (p.Val80Gly)
c.389T>G (p.Val130Gly)
c.362T>G (p.Val121Gly)
7g.150958436A>GCA369863380KCNH2n.1372T>C
c.539T>C (p.Val180Ala)
c.235-44T>C (n.235-44T>C)
n.762T>C
c.239T>C (p.Val80Ala)
c.389T>C (p.Val130Ala)
c.362T>C (p.Val121Ala)
gnomAD v4
7g.150958436A>TCA369863382KCNH2n.1372T>A
c.539T>A (p.Val180Glu)
c.235-44T>A (n.235-44T>A)
n.762T>A
c.239T>A (p.Val80Glu)
c.389T>A (p.Val130Glu)
c.362T>A (p.Val121Glu)
7g.150958437C>ACA369863384KCNH2n.1371G>T
c.538G>T (p.Val180Leu)
c.235-45G>T (n.235-45G>T)
n.761G>T
c.238G>T (p.Val80Leu)
c.388G>T (p.Val130Leu)
c.361G>T (p.Val121Leu)
7g.150958437C>GCA369863386KCNH2n.1371G>C
c.538G>C (p.Val180Leu)
c.235-45G>C (n.235-45G>C)
n.761G>C
c.238G>C (p.Val80Leu)
c.388G>C (p.Val130Leu)
c.361G>C (p.Val121Leu)
7g.150958437C>TCA369863388KCNH2n.1371G>A
c.538G>A (p.Val180Met)
c.235-45G>A (n.235-45G>A)
n.761G>A
c.238G>A (p.Val80Met)
c.388G>A (p.Val130Met)
c.361G>A (p.Val121Met)
gnomAD v4
7g.150958438C>ACA458646820KCNH2n.1370G>T
c.537G>T (p.Ser179=)
c.235-46G>T (n.235-46G>T)
n.760G>T
c.237G>T (p.Ser79=)
c.387G>T (p.Ser129=)
c.360G>T (p.Ser120=)
gnomAD v4
7g.150958438C>GCA458646821KCNH2n.1370G>C
c.537G>C (p.Ser179=)
c.235-46G>C (n.235-46G>C)
n.760G>C
c.237G>C (p.Ser79=)
c.387G>C (p.Ser129=)
c.360G>C (p.Ser120=)
7g.150958438C>TCA458646822KCNH2n.1370G>A
c.537G>A (p.Ser179=)
c.235-46G>A (n.235-46G>A)
n.760G>A
c.237G>A (p.Ser79=)
c.387G>A (p.Ser129=)
c.360G>A (p.Ser120=)
ClinVar gnomAD v4
7g.150958438_150958463delinsCGACGACTCCCGGGCCGTCAGCGCCACA1752418705KCNH2n.1345_1370delinsTGGCGCTGACGGCCCGGGAGTCGTCG
c.512_537delinsTGGCGCTGACGGCCCGGGAGTCGTCG (p.Leu171=)
c.235-71_235-46delinsTGGCGCTGACGGCCCGGGAGTCGTCG (n.235-71_235-46delinsTGGCGCTGACGGCCCGGGAGTCGTCG)
n.735_760delinsTGGCGCTGACGGCCCGGGAGTCGTCG
c.212_237delinsTGGCGCTGACGGCCCGGGAGTCGTCG (p.Leu71=)
c.362_387delinsTGGCGCTGACGGCCCGGGAGTCGTCG (p.Leu121=)
c.335_360delinsTGGCGCTGACGGCCCGGGAGTCGTCG (p.Leu112=)
7g.150958439G>ACA369863394KCNH2n.1369C>T
c.536C>T (p.Ser179Leu)
c.235-47C>T (n.235-47C>T)
n.759C>T
c.236C>T (p.Ser79Leu)
c.386C>T (p.Ser129Leu)
c.359C>T (p.Ser120Leu)
ClinVar dbSNP gnomAD v4
7g.150958439G>CCA369863390KCNH2n.1369C>G
c.536C>G (p.Ser179Trp)
c.235-47C>G (n.235-47C>G)
n.759C>G
c.236C>G (p.Ser79Trp)
c.386C>G (p.Ser129Trp)
c.359C>G (p.Ser120Trp)
dbSNP gnomAD v2 gnomAD v4
7g.150958439G=CA1752418709KCNH2n.1369C=
c.536C= (p.Ser179=)
c.235-47C= (n.235-47C=)
n.759C=
c.236C= (p.Ser79=)
c.386C= (p.Ser129=)
c.359C= (p.Ser120=)
7g.150958439G>TCA369863392KCNH2n.1369C>A
c.536C>A (p.Ser179Ter)
c.235-47C>A (n.235-47C>A)
n.759C>A
c.236C>A (p.Ser79Ter)
c.386C>A (p.Ser129Ter)
c.359C>A (p.Ser120Ter)
gnomAD v4
7g.150958440_150958464delCA658797051KCNH2n.1345_1369del
c.512_536del (p.Leu171ArgfsTer22)
c.235-71_235-47del (n.235-71_235-47del)
n.735_759del
c.212_236del (p.Leu71ArgfsTer22)
c.362_386del (p.Leu121ArgfsTer22)
c.335_359del (p.Leu112ArgfsTer22)
ClinVar dbSNP
7g.150958440A>CCA369863396KCNH2n.1368T>G
c.535T>G (p.Ser179Ala)
c.235-48T>G (n.235-48T>G)
n.758T>G
c.235T>G (p.Ser79Ala)
c.385T>G (p.Ser129Ala)
c.358T>G (p.Ser120Ala)
ClinVar dbSNP
7g.150958440A>GCA369863398KCNH2n.1368T>C
c.535T>C (p.Ser179Pro)
c.235-48T>C (n.235-48T>C)
n.758T>C
c.235T>C (p.Ser79Pro)
c.385T>C (p.Ser129Pro)
c.358T>C (p.Ser120Pro)
gnomAD v4
7g.150958440A>TCA369863400KCNH2n.1368T>A
c.535T>A (p.Ser179Thr)
c.235-48T>A (n.235-48T>A)
n.758T>A
c.235T>A (p.Ser79Thr)
c.385T>A (p.Ser129Thr)
c.358T>A (p.Ser120Thr)
7g.150958441C>ACA458646823KCNH2n.1367G>T
c.534G>T (p.Ser178=)
c.235-49G>T (n.235-49G>T)
n.757G>T
c.234G>T (p.Ser78=)
c.384G>T (p.Ser128=)
c.357G>T (p.Ser119=)
ClinVar gnomAD v4
7g.150958441C=CA1752418712KCNH2n.1367G=
c.534G= (p.Ser178=)
c.235-49G= (n.235-49G=)
n.757G=
c.234G= (p.Ser78=)
c.384G= (p.Ser128=)
c.357G= (p.Ser119=)
7g.150958441C>GCA169081479KCNH2n.1367G>C
c.534G>C (p.Ser178=)
c.235-49G>C (n.235-49G>C)
n.757G>C
c.234G>C (p.Ser78=)
c.384G>C (p.Ser128=)
c.357G>C (p.Ser119=)
ClinVar dbSNP gnomAD v3 gnomAD v4
7g.150958441C>TCA458646824KCNH2n.1367G>A
c.534G>A (p.Ser178=)
c.235-49G>A (n.235-49G>A)
n.757G>A
c.234G>A (p.Ser78=)
c.384G>A (p.Ser128=)
c.357G>A (p.Ser119=)
ClinVar dbSNP gnomAD v2 gnomAD v4
7g.150958442G>ACA369863402KCNH2n.1366C>T
c.533C>T (p.Ser178Leu)
c.235-50C>T (n.235-50C>T)
n.756C>T
c.233C>T (p.Ser78Leu)
c.383C>T (p.Ser128Leu)
c.356C>T (p.Ser119Leu)
gnomAD v4
7g.150958442G>CCA369863403KCNH2n.1366C>G
c.533C>G (p.Ser178Trp)
c.235-50C>G (n.235-50C>G)
n.756C>G
c.233C>G (p.Ser78Trp)
c.383C>G (p.Ser128Trp)
c.356C>G (p.Ser119Trp)
7g.150958442G>TCA369863405KCNH2n.1366C>A
c.533C>A (p.Ser178Ter)
c.235-50C>A (n.235-50C>A)
n.756C>A
c.233C>A (p.Ser78Ter)
c.383C>A (p.Ser128Ter)
c.356C>A (p.Ser119Ter)
gnomAD v4
7g.150958443A>CCA369863406KCNH2n.1365T>G
c.532T>G (p.Ser178Ala)
c.235-51T>G (n.235-51T>G)
n.755T>G
c.232T>G (p.Ser78Ala)
c.382T>G (p.Ser128Ala)
c.355T>G (p.Ser119Ala)
7g.150958443A>GCA369863408KCNH2n.1365T>C
c.532T>C (p.Ser178Pro)
c.235-51T>C (n.235-51T>C)
n.755T>C
c.232T>C (p.Ser78Pro)
c.382T>C (p.Ser128Pro)
c.355T>C (p.Ser119Pro)
ClinVar
7g.150958443A>TCA369863410KCNH2n.1365T>A
c.532T>A (p.Ser178Thr)
c.235-51T>A (n.235-51T>A)
n.755T>A
c.232T>A (p.Ser78Thr)
c.382T>A (p.Ser128Thr)
c.355T>A (p.Ser119Thr)
7g.150958444C>ACA369863412KCNH2n.1364G>T
c.531G>T (p.Glu177Asp)
c.235-52G>T (n.235-52G>T)
n.754G>T
c.231G>T (p.Glu77Asp)
c.381G>T (p.Glu127Asp)
c.354G>T (p.Glu118Asp)
gnomAD v4
7g.150958444C>GCA369863413KCNH2n.1364G>C
c.531G>C (p.Glu177Asp)
c.235-52G>C (n.235-52G>C)
n.754G>C
c.231G>C (p.Glu77Asp)
c.381G>C (p.Glu127Asp)
c.354G>C (p.Glu118Asp)
7g.150958444C>TCA458646825KCNH2n.1364G>A
c.531G>A (p.Glu177=)
c.235-52G>A (n.235-52G>A)
n.754G>A
c.231G>A (p.Glu77=)
c.381G>A (p.Glu127=)
c.354G>A (p.Glu118=)
7g.150958445T>ACA369863419KCNH2n.1363A>T
c.530A>T (p.Glu177Val)
c.235-53A>T (n.235-53A>T)
n.753A>T
c.230A>T (p.Glu77Val)
c.380A>T (p.Glu127Val)
c.353A>T (p.Glu118Val)
7g.150958445T>CCA369863417KCNH2n.1363A>G
c.530A>G (p.Glu177Gly)
c.235-53A>G (n.235-53A>G)
n.753A>G
c.230A>G (p.Glu77Gly)
c.380A>G (p.Glu127Gly)
c.353A>G (p.Glu118Gly)
gnomAD v4
7g.150958445T>GCA369863415KCNH2n.1363A>C
c.530A>C (p.Glu177Ala)
c.235-53A>C (n.235-53A>C)
n.753A>C
c.230A>C (p.Glu77Ala)
c.380A>C (p.Glu127Ala)
c.353A>C (p.Glu118Ala)
ClinVar dbSNP gnomAD v4
7g.150958445T=CA1752418715KCNH2n.1363A=
c.530A= (p.Glu177=)
c.235-53A= (n.235-53A=)
n.753A=
c.230A= (p.Glu77=)
c.380A= (p.Glu127=)
c.353A= (p.Glu118=)
7g.150958446C>ACA369863421KCNH2n.1362G>T
c.529G>T (p.Glu177Ter)
c.235-54G>T (n.235-54G>T)
n.752G>T
c.229G>T (p.Glu77Ter)
c.379G>T (p.Glu127Ter)
c.352G>T (p.Glu118Ter)
ClinVar gnomAD v4
7g.150958446C>GCA369863423KCNH2n.1362G>C
c.529G>C (p.Glu177Gln)
c.235-54G>C (n.235-54G>C)
n.752G>C
c.229G>C (p.Glu77Gln)
c.379G>C (p.Glu127Gln)
c.352G>C (p.Glu118Gln)
7g.150958446C>TCA369863425KCNH2n.1362G>A
c.529G>A (p.Glu177Lys)
c.235-54G>A (n.235-54G>A)
n.752G>A
c.229G>A (p.Glu77Lys)
c.379G>A (p.Glu127Lys)
c.352G>A (p.Glu118Lys)
gnomAD v4

Number of alleles fetched