Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.150958053_150958148delCA2580077681KCNH2n.1665_1749+11del
c.832_916+11del
c.484_568+11del
n.1055_1139+11del
c.532_616+11del
c.682_766+11del
c.655_739+11del
 ClinVar
7g.150958054_150958116delCA2695208628KCNH2n.1693_1749+6del
c.860_916+6del
c.512_568+6del
n.1083_1139+6del
c.560_616+6del
c.710_766+6del
c.683_739+6del
7g.150958091_150958151delCA2685607217KCNH2n.1662_1722del
c.829_889del (p.Ala277ProfsTer?)
c.481_541del (p.Ala161ProfsTer?)
n.1052_1112del
c.529_589del (p.Ala177ProfsTer?)
c.679_739del (p.Ala227ProfsTer?)
c.652_712del (p.Ala218ProfsTer?)
 gnomAD v4
7g.150958106_150958114delCA2685607281KCNH2n.1697_1705del
c.864_872del (p.Ile288_Ala290del)
c.516_524del (p.Ile172_Ala174del)
n.1087_1095del
c.564_572del (p.Ile188_Ala190del)
c.714_722del (p.Ile238_Ala240del)
c.687_695del (p.Ile229_Ala231del)
 gnomAD v4
7g.150958107_150958111dupCA2580077685KCNH2n.1698_1702dup
c.865_869dup (p.Met291ArgfsTer?)
c.517_521dup (p.Met175ArgfsTer?)
n.1088_1092dup
c.565_569dup (p.Met191ArgfsTer?)
c.715_719dup (p.Met241ArgfsTer?)
c.688_692dup (p.Met232ArgfsTer?)
 ClinVar
7g.150958106_150958125delinsGCCTCGATGTCGTCGGCCGACA1752417828KCNH2n.1683_1702delinsTCGGCCGACGACATCGAGGC
c.850_869delinsTCGGCCGACGACATCGAGGC (p.Ser284=)
c.502_521delinsTCGGCCGACGACATCGAGGC (p.Ser168=)
n.1073_1092delinsTCGGCCGACGACATCGAGGC
c.550_569delinsTCGGCCGACGACATCGAGGC (p.Ser184=)
c.700_719delinsTCGGCCGACGACATCGAGGC (p.Ser234=)
c.673_692delinsTCGGCCGACGACATCGAGGC (p.Ser225=)
7g.150958108_150958126delCA008896KCNH2n.1683_1701del
c.850_868del (p.Ser284ProfsTer?)
c.502_520del (p.Ser168ProfsTer?)
n.1073_1091del
c.550_568del (p.Ser184ProfsTer?)
c.700_718del (p.Ser234ProfsTer?)
c.673_691del (p.Ser225ProfsTer?)
 ClinVar dbSNP
7g.150958108C>ACA369862213KCNH2n.1700G>T
c.867G>T (p.Glu289Asp)
c.519G>T (p.Glu173Asp)
n.1090G>T
c.567G>T (p.Glu189Asp)
c.717G>T (p.Glu239Asp)
c.690G>T (p.Glu230Asp)
 gnomAD v4
7g.150958108C=CA1752417845KCNH2n.1700G=
c.867G= (p.Glu289=)
c.519G= (p.Glu173=)
n.1090G=
c.567G= (p.Glu189=)
c.717G= (p.Glu239=)
c.690G= (p.Glu230=)
7g.150958108C>GCA369862215KCNH2n.1700G>C
c.867G>C (p.Glu289Asp)
c.519G>C (p.Glu173Asp)
n.1090G>C
c.567G>C (p.Glu189Asp)
c.717G>C (p.Glu239Asp)
c.690G>C (p.Glu230Asp)
 dbSNP gnomAD v4
7g.150958108C>TCA458871818KCNH2n.1700G>A
c.867G>A (p.Glu289=)
c.519G>A (p.Glu173=)
n.1090G>A
c.567G>A (p.Glu189=)
c.717G>A (p.Glu239=)
c.690G>A (p.Glu230=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.150958109T>ACA369862217KCNH2n.1699A>T
c.866A>T (p.Glu289Val)
c.518A>T (p.Glu173Val)
n.1089A>T
c.566A>T (p.Glu189Val)
c.716A>T (p.Glu239Val)
c.689A>T (p.Glu230Val)
 gnomAD v4
7g.150958109T>CCA369862219KCNH2n.1699A>G
c.866A>G (p.Glu289Gly)
c.518A>G (p.Glu173Gly)
n.1089A>G
c.566A>G (p.Glu189Gly)
c.716A>G (p.Glu239Gly)
c.689A>G (p.Glu230Gly)
 ClinVar gnomAD v4
7g.150958109T>GCA369862221KCNH2n.1699A>C
c.866A>C (p.Glu289Ala)
c.518A>C (p.Glu173Ala)
n.1089A>C
c.566A>C (p.Glu189Ala)
c.716A>C (p.Glu239Ala)
c.689A>C (p.Glu230Ala)
7g.150958112_150958120delCA2685607313KCNH2n.1691_1699del
c.858_866del (p.Asp286_Ile288del)
c.510_518del (p.Asp170_Ile172del)
n.1081_1089del
c.558_566del (p.Asp186_Ile188del)
c.708_716del (p.Asp236_Ile238del)
c.681_689del (p.Asp227_Ile229del)
 gnomAD v4
7g.150958110C>ACA369862225KCNH2n.1698G>T
c.865G>T (p.Glu289Ter)
c.517G>T (p.Glu173Ter)
n.1088G>T
c.565G>T (p.Glu189Ter)
c.715G>T (p.Glu239Ter)
c.688G>T (p.Glu230Ter)
 gnomAD v4
7g.150958110C=CA1752417849KCNH2n.1698G=
c.865G= (p.Glu289=)
c.517G= (p.Glu173=)
n.1088G=
c.565G= (p.Glu189=)
c.715G= (p.Glu239=)
c.688G= (p.Glu230=)
7g.150958110C>GCA369862224KCNH2n.1698G>C
c.865G>C (p.Glu289Gln)
c.517G>C (p.Glu173Gln)
n.1088G>C
c.565G>C (p.Glu189Gln)
c.715G>C (p.Glu239Gln)
c.688G>C (p.Glu230Gln)
 ClinVar dbSNP gnomAD v4
7g.150958110C>TCA008907KCNH2n.1698G>A
c.865G>A (p.Glu289Lys)
c.517G>A (p.Glu173Lys)
n.1088G>A
c.565G>A (p.Glu189Lys)
c.715G>A (p.Glu239Lys)
c.688G>A (p.Glu230Lys)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150958113_150958128delCA2579988140KCNH2n.1683_1698del
c.850_865del (p.Ser284ArgfsTer?)
c.502_517del (p.Ser168ArgfsTer?)
n.1073_1088del
c.550_565del (p.Ser184ArgfsTer?)
c.700_715del (p.Ser234ArgfsTer?)
c.673_688del (p.Ser225ArgfsTer?)
7g.150958111G>ACA072164KCNH2n.1697C>T
c.864C>T (p.Ile288=)
c.516C>T (p.Ile172=)
n.1087C>T
c.564C>T (p.Ile188=)
c.714C>T (p.Ile238=)
c.687C>T (p.Ile229=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150958111G>CCA369862227KCNH2n.1697C>G
c.864C>G (p.Ile288Met)
c.516C>G (p.Ile172Met)
n.1087C>G
c.564C>G (p.Ile188Met)
c.714C>G (p.Ile238Met)
c.687C>G (p.Ile229Met)
 gnomAD v4
7g.150958111G=CA1752417857KCNH2n.1697C=
c.864C= (p.Ile288=)
c.516C= (p.Ile172=)
n.1087C=
c.564C= (p.Ile188=)
c.714C= (p.Ile238=)
c.687C= (p.Ile229=)
7g.150958111G>TCA458871825KCNH2n.1697C>A
c.864C>A (p.Ile288=)
c.516C>A (p.Ile172=)
n.1087C>A
c.564C>A (p.Ile188=)
c.714C>A (p.Ile238=)
c.687C>A (p.Ile229=)
 gnomAD v4
7g.150958112A=CA1752417865KCNH2n.1696T=
c.863T= (p.Ile288=)
c.515T= (p.Ile172=)
n.1086T=
c.563T= (p.Ile188=)
c.713T= (p.Ile238=)
c.686T= (p.Ile229=)
7g.150958112A>CCA369862229KCNH2n.1696T>G
c.863T>G (p.Ile288Ser)
c.515T>G (p.Ile172Ser)
n.1086T>G
c.563T>G (p.Ile188Ser)
c.713T>G (p.Ile238Ser)
c.686T>G (p.Ile229Ser)
7g.150958112A>GCA369862231KCNH2n.1696T>C
c.863T>C (p.Ile288Thr)
c.515T>C (p.Ile172Thr)
n.1086T>C
c.563T>C (p.Ile188Thr)
c.713T>C (p.Ile238Thr)
c.686T>C (p.Ile229Thr)
 ClinVar dbSNP gnomAD v4
7g.150958112A>TCA369862232KCNH2n.1696T>A
c.863T>A (p.Ile288Asn)
c.515T>A (p.Ile172Asn)
n.1086T>A
c.563T>A (p.Ile188Asn)
c.713T>A (p.Ile238Asn)
c.686T>A (p.Ile229Asn)
7g.150958113T>ACA369862233KCNH2n.1695A>T
c.862A>T (p.Ile288Phe)
c.514A>T (p.Ile172Phe)
n.1085A>T
c.562A>T (p.Ile188Phe)
c.712A>T (p.Ile238Phe)
c.685A>T (p.Ile229Phe)
7g.150958113T>CCA369862235KCNH2n.1695A>G
c.862A>G (p.Ile288Val)
c.514A>G (p.Ile172Val)
n.1085A>G
c.562A>G (p.Ile188Val)
c.712A>G (p.Ile238Val)
c.685A>G (p.Ile229Val)
 gnomAD v4
7g.150958113T>GCA369862237KCNH2n.1695A>C
c.862A>C (p.Ile288Leu)
c.514A>C (p.Ile172Leu)
n.1085A>C
c.562A>C (p.Ile188Leu)
c.712A>C (p.Ile238Leu)
c.685A>C (p.Ile229Leu)
7g.150958114G>ACA458871828KCNH2n.1694C>T
c.861C>T (p.Asp287=)
c.513C>T (p.Asp171=)
n.1084C>T
c.561C>T (p.Asp187=)
c.711C>T (p.Asp237=)
c.684C>T (p.Asp228=)
 gnomAD v4
7g.150958114G>CCA369862239KCNH2n.1694C>G
c.861C>G (p.Asp287Glu)
c.513C>G (p.Asp171Glu)
n.1084C>G
c.561C>G (p.Asp187Glu)
c.711C>G (p.Asp237Glu)
c.684C>G (p.Asp228Glu)
7g.150958114G>TCA369862241KCNH2n.1694C>A
c.861C>A (p.Asp287Glu)
c.513C>A (p.Asp171Glu)
n.1084C>A
c.561C>A (p.Asp187Glu)
c.711C>A (p.Asp237Glu)
c.684C>A (p.Asp228Glu)
 gnomAD v4
7g.150958118_150958120dupCA2580614281KCNH2n.1692_1694dup
c.859_861dup (p.Asp287_Ile288insAsp)
c.511_513dup (p.Asp171_Ile172insAsp)
n.1082_1084dup
c.559_561dup (p.Asp187_Ile188insAsp)
c.709_711dup (p.Asp237_Ile238insAsp)
c.682_684dup (p.Asp228_Ile229insAsp)
 ClinVar dbSNP gnomAD v4
7g.150958115T>ACA369862243KCNH2n.1693A>T
c.860A>T (p.Asp287Val)
c.512A>T (p.Asp171Val)
n.1083A>T
c.560A>T (p.Asp187Val)
c.710A>T (p.Asp237Val)
c.683A>T (p.Asp228Val)
7g.150958115T>CCA369862245KCNH2n.1693A>G
c.860A>G (p.Asp287Gly)
c.512A>G (p.Asp171Gly)
n.1083A>G
c.560A>G (p.Asp187Gly)
c.710A>G (p.Asp237Gly)
c.683A>G (p.Asp228Gly)
 ClinVar gnomAD v4
7g.150958115T>GCA369862247KCNH2n.1693A>C
c.860A>C (p.Asp287Ala)
c.512A>C (p.Asp171Ala)
n.1083A>C
c.560A>C (p.Asp187Ala)
c.710A>C (p.Asp237Ala)
c.683A>C (p.Asp228Ala)
7g.150958115_150958122delinsTCGTCGGCCA1752417868KCNH2n.1686_1693delinsGCCGACGA
c.853_860delinsGCCGACGA (p.Ala285=)
c.505_512delinsGCCGACGA (p.Ala169=)
n.1076_1083delinsGCCGACGA
c.553_560delinsGCCGACGA (p.Ala185=)
c.703_710delinsGCCGACGA (p.Ala235=)
c.676_683delinsGCCGACGA (p.Ala226=)
7g.150958116C>ACA369862254KCNH2n.1692G>T
c.859G>T (p.Asp287Tyr)
c.511G>T (p.Asp171Tyr)
n.1082G>T
c.559G>T (p.Asp187Tyr)
c.709G>T (p.Asp237Tyr)
c.682G>T (p.Asp228Tyr)
 gnomAD v4
7g.150958116C=CA1752417874KCNH2n.1692G=
c.859G= (p.Asp287=)
c.511G= (p.Asp171=)
n.1082G=
c.559G= (p.Asp187=)
c.709G= (p.Asp237=)
c.682G= (p.Asp228=)
7g.150958116C>GCA369862252KCNH2n.1692G>C
c.859G>C (p.Asp287His)
c.511G>C (p.Asp171His)
n.1082G>C
c.559G>C (p.Asp187His)
c.709G>C (p.Asp237His)
c.682G>C (p.Asp228His)
7g.150958116C>TCA369862250KCNH2n.1692G>A
c.859G>A (p.Asp287Asn)
c.511G>A (p.Asp171Asn)
n.1082G>A
c.559G>A (p.Asp187Asn)
c.709G>A (p.Asp237Asn)
c.682G>A (p.Asp228Asn)
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.150958118_150958124dupCA2695208631KCNH2n.1686_1692dup
c.853_859dup (p.Asp287GlyfsTer?)
c.505_511dup (p.Asp171GlyfsTer?)
n.1076_1082dup
c.553_559dup (p.Asp187GlyfsTer?)
c.703_709dup (p.Asp237GlyfsTer?)
c.676_682dup (p.Asp228GlyfsTer?)
7g.150958118_150958124delCA008902KCNH2n.1686_1692del
c.853_859del (p.Ala285ThrfsTer?)
c.505_511del (p.Ala169ThrfsTer?)
n.1076_1082del
c.553_559del (p.Ala185ThrfsTer?)
c.703_709del (p.Ala235ThrfsTer?)
c.676_682del (p.Ala226ThrfsTer?)
 ClinVar dbSNP
7g.150958117G>ACA458871833KCNH2n.1691C>T
c.858C>T (p.Asp286=)
c.510C>T (p.Asp170=)
n.1081C>T
c.558C>T (p.Asp186=)
c.708C>T (p.Asp236=)
c.681C>T (p.Asp227=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150958117G>CCA369862258KCNH2n.1691C>G
c.858C>G (p.Asp286Glu)
c.510C>G (p.Asp170Glu)
n.1081C>G
c.558C>G (p.Asp186Glu)
c.708C>G (p.Asp236Glu)
c.681C>G (p.Asp227Glu)
7g.150958117G=CA1752417877KCNH2n.1691C=
c.858C= (p.Asp286=)
c.510C= (p.Asp170=)
n.1081C=
c.558C= (p.Asp186=)
c.708C= (p.Asp236=)
c.681C= (p.Asp227=)
7g.150958117G>TCA369862256KCNH2n.1691C>A
c.858C>A (p.Asp286Glu)
c.510C>A (p.Asp170Glu)
n.1081C>A
c.558C>A (p.Asp186Glu)
c.708C>A (p.Asp236Glu)
c.681C>A (p.Asp227Glu)
 gnomAD v4
7g.150958118T>ACA369862263KCNH2n.1690A>T
c.857A>T (p.Asp286Val)
c.509A>T (p.Asp170Val)
n.1080A>T
c.557A>T (p.Asp186Val)
c.707A>T (p.Asp236Val)
c.680A>T (p.Asp227Val)
 gnomAD v4

Number of alleles fetched