Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.150958121_150958206delinsACGCCTCGGGCTCCA2697549692KCNH2n.1602_1687delinsGAGCCCGAGGCGT
c.769_854delinsGAGCCCGAGGCGT (p.Asn257GlufsTer?)
c.421_506delinsGAGCCCGAGGCGT (p.Asn141GlufsTer?)
n.992_1077delinsGAGCCCGAGGCGT
c.469_554delinsGAGCCCGAGGCGT (p.Asn157GlufsTer?)
c.619_704delinsGAGCCCGAGGCGT (p.Asn207GlufsTer?)
c.592_677delinsGAGCCCGAGGCGT (p.Asn198GlufsTer?)
7g.150958156_150958168delCA2573141814KCNH2n.1642_1654del
c.809_821del (p.Thr270LysfsTer?)
c.461_473del (p.Thr154LysfsTer?)
n.1032_1044del
c.509_521del (p.Thr170LysfsTer?)
c.659_671del (p.Thr220LysfsTer?)
c.632_644del (p.Thr211LysfsTer?)
ClinVar dbSNP
7g.150958159_150958164dupCA2580077687KCNH2n.1646_1651dup
c.813_818dup (p.Arg273_Glu274insSerArg)
c.465_470dup (p.Arg157_Glu158insSerArg)
n.1036_1041dup
c.513_518dup (p.Arg173_Glu174insSerArg)
c.663_668dup (p.Arg223_Glu224insSerArg)
c.636_641dup (p.Arg214_Glu215insSerArg)
ClinVar
7g.150958161_150958163delinsAGCCA1752417984KCNH2n.1645_1647delinsGCT
c.812_814delinsGCT (p.Arg271=)
c.464_466delinsGCT (p.Arg155=)
n.1035_1037delinsGCT
c.512_514delinsGCT (p.Arg171=)
c.662_664delinsGCT (p.Arg221=)
c.635_637delinsGCT (p.Arg212=)
7g.150958162_150958166delinsGCGCGCA1752417988KCNH2n.1642_1646delinsCGCGC
c.809_813delinsCGCGC (p.Thr270=)
c.461_465delinsCGCGC (p.Thr154=)
n.1032_1036delinsCGCGC
c.509_513delinsCGCGC (p.Thr170=)
c.659_663delinsCGCGC (p.Thr220=)
c.632_636delinsCGCGC (p.Thr211=)
7g.150958165_150958166delCA1752417986KCNH2n.1645_1646del
c.812_813del (p.Arg271LeufsTer?)
c.464_465del (p.Arg155LeufsTer?)
n.1035_1036del
c.512_513del (p.Arg171LeufsTer?)
c.662_663del (p.Arg221LeufsTer?)
c.635_636del (p.Arg212LeufsTer?)
dbSNP
7g.150958163C>ACA369862392KCNH2n.1645G>T
c.812G>T (p.Arg271Leu)
c.464G>T (p.Arg155Leu)
n.1035G>T
c.512G>T (p.Arg171Leu)
c.662G>T (p.Arg221Leu)
c.635G>T (p.Arg212Leu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150958163C=CA1752417992KCNH2n.1645G=
c.812G= (p.Arg271=)
c.464G= (p.Arg155=)
n.1035G=
c.512G= (p.Arg171=)
c.662G= (p.Arg221=)
c.635G= (p.Arg212=)
7g.150958163C>GCA369862396KCNH2n.1645G>C
c.812G>C (p.Arg271Pro)
c.464G>C (p.Arg155Pro)
n.1035G>C
c.512G>C (p.Arg171Pro)
c.662G>C (p.Arg221Pro)
c.635G>C (p.Arg212Pro)
gnomAD v4
7g.150958163C>TCA008845KCNH2n.1645G>A
c.812G>A (p.Arg271His)
c.464G>A (p.Arg155His)
n.1035G>A
c.512G>A (p.Arg171His)
c.662G>A (p.Arg221His)
c.635G>A (p.Arg212His)
ClinVar dbSNP gnomAD v2 gnomAD v4
7g.150958163_150958166delinsGCTTTTCA008822KCNH2n.1642_1645delinsAAAAGC
c.809_812delinsAAAAGC (p.Thr270LysfsTer?)
c.461_464delinsAAAAGC (p.Thr154LysfsTer?)
n.1032_1035delinsAAAAGC
c.509_512delinsAAAAGC (p.Thr170LysfsTer?)
c.659_662delinsAAAAGC (p.Thr220LysfsTer?)
c.632_635delinsAAAAGC (p.Thr211LysfsTer?)
ClinVar dbSNP
7g.150958163_150958164insTCA658797047KCNH2n.1644_1645insA
c.811_812insA (p.Arg271GlnfsTer?)
c.463_464insA (p.Arg155GlnfsTer?)
n.1034_1035insA
c.511_512insA (p.Arg171GlnfsTer?)
c.661_662insA (p.Arg221GlnfsTer?)
c.634_635insA (p.Arg212GlnfsTer?)
ClinVar dbSNP
7g.150958164G>ACA369862398KCNH2n.1644C>T
c.811C>T (p.Arg271Cys)
c.463C>T (p.Arg155Cys)
n.1034C>T
c.511C>T (p.Arg171Cys)
c.661C>T (p.Arg221Cys)
c.634C>T (p.Arg212Cys)
dbSNP gnomAD v4
7g.150958164G>CCA369862400KCNH2n.1644C>G
c.811C>G (p.Arg271Gly)
c.463C>G (p.Arg155Gly)
n.1034C>G
c.511C>G (p.Arg171Gly)
c.661C>G (p.Arg221Gly)
c.634C>G (p.Arg212Gly)
gnomAD v4
7g.150958164G=CA1752418000KCNH2n.1644C=
c.811C= (p.Arg271=)
c.463C= (p.Arg155=)
n.1034C=
c.511C= (p.Arg171=)
c.661C= (p.Arg221=)
c.634C= (p.Arg212=)
7g.150958164G>TCA369862401KCNH2n.1644C>A
c.811C>A (p.Arg271Ser)
c.463C>A (p.Arg155Ser)
n.1034C>A
c.511C>A (p.Arg171Ser)
c.661C>A (p.Arg221Ser)
c.634C>A (p.Arg212Ser)
gnomAD v4
7g.150958165C>ACA458871935KCNH2n.1643G>T
c.810G>T (p.Thr270=)
c.462G>T (p.Thr154=)
n.1033G>T
c.510G>T (p.Thr170=)
c.660G>T (p.Thr220=)
c.633G>T (p.Thr211=)
gnomAD v4
7g.150958165C=CA1752418002KCNH2n.1643G=
c.810G= (p.Thr270=)
c.462G= (p.Thr154=)
n.1033G=
c.510G= (p.Thr170=)
c.660G= (p.Thr220=)
c.633G= (p.Thr211=)
7g.150958165C>GCA458871933KCNH2n.1643G>C
c.810G>C (p.Thr270=)
c.462G>C (p.Thr154=)
n.1033G>C
c.510G>C (p.Thr170=)
c.660G>C (p.Thr220=)
c.633G>C (p.Thr211=)
7g.150958165C>TCA458871934KCNH2n.1643G>A
c.810G>A (p.Thr270=)
c.462G>A (p.Thr154=)
n.1033G>A
c.510G>A (p.Thr170=)
c.660G>A (p.Thr220=)
c.633G>A (p.Thr211=)
ClinVar dbSNP gnomAD v3 gnomAD v4
7g.150958166G>ACA369862404KCNH2n.1642C>T
c.809C>T (p.Thr270Met)
c.461C>T (p.Thr154Met)
n.1032C>T
c.509C>T (p.Thr170Met)
c.659C>T (p.Thr220Met)
c.632C>T (p.Thr211Met)
ClinVar dbSNP gnomAD v3 gnomAD v4
7g.150958166G>CCA369862408KCNH2n.1642C>G
c.809C>G (p.Thr270Arg)
c.461C>G (p.Thr154Arg)
n.1032C>G
c.509C>G (p.Thr170Arg)
c.659C>G (p.Thr220Arg)
c.632C>G (p.Thr211Arg)
dbSNP gnomAD v4
7g.150958166G=CA1752418004KCNH2n.1642C=
c.809C= (p.Thr270=)
c.461C= (p.Thr154=)
n.1032C=
c.509C= (p.Thr170=)
c.659C= (p.Thr220=)
c.632C= (p.Thr211=)
7g.150958166G>TCA369862406KCNH2n.1642C>A
c.809C>A (p.Thr270Lys)
c.461C>A (p.Thr154Lys)
n.1032C>A
c.509C>A (p.Thr170Lys)
c.659C>A (p.Thr220Lys)
c.632C>A (p.Thr211Lys)
dbSNP gnomAD v4
7g.150958166_150958170delinsGTCCGCA1752418007KCNH2n.1638_1642delinsCGGAC
c.805_809delinsCGGAC (p.Arg269=)
c.457_461delinsCGGAC (p.Arg153=)
n.1028_1032delinsCGGAC
c.505_509delinsCGGAC (p.Arg169=)
c.655_659delinsCGGAC (p.Arg219=)
c.628_632delinsCGGAC (p.Arg210=)
7g.150958167T>ACA369862409KCNH2n.1641A>T
c.808A>T (p.Thr270Ser)
c.460A>T (p.Thr154Ser)
n.1031A>T
c.508A>T (p.Thr170Ser)
c.658A>T (p.Thr220Ser)
c.631A>T (p.Thr211Ser)
7g.150958167T>CCA369862411KCNH2n.1641A>G
c.808A>G (p.Thr270Ala)
c.460A>G (p.Thr154Ala)
n.1031A>G
c.508A>G (p.Thr170Ala)
c.658A>G (p.Thr220Ala)
c.631A>G (p.Thr211Ala)
dbSNP gnomAD v4
7g.150958167T>GCA369862412KCNH2n.1641A>C
c.808A>C (p.Thr270Pro)
c.460A>C (p.Thr154Pro)
n.1031A>C
c.508A>C (p.Thr170Pro)
c.658A>C (p.Thr220Pro)
c.631A>C (p.Thr211Pro)
7g.150958167_150958170delinsACTCA658797048KCNH2n.1638_1641delinsAGT
c.805_808delinsAGT (p.Arg269SerfsTer?)
c.457_460delinsAGT (p.Arg153SerfsTer?)
n.1028_1031delinsAGT
c.505_508delinsAGT (p.Arg169SerfsTer?)
c.655_658delinsAGT (p.Arg219SerfsTer?)
c.628_631delinsAGT (p.Arg210SerfsTer?)
ClinVar dbSNP
7g.150958168C>ACA458871941KCNH2n.1640G>T
c.807G>T (p.Arg269=)
c.459G>T (p.Arg153=)
n.1030G>T
c.507G>T (p.Arg169=)
c.657G>T (p.Arg219=)
c.630G>T (p.Arg210=)
gnomAD v4
7g.150958168C>GCA458871943KCNH2n.1640G>C
c.807G>C (p.Arg269=)
c.459G>C (p.Arg153=)
n.1030G>C
c.507G>C (p.Arg169=)
c.657G>C (p.Arg219=)
c.630G>C (p.Arg210=)
gnomAD v4
7g.150958168C>TCA458871942KCNH2n.1640G>A
c.807G>A (p.Arg269=)
c.459G>A (p.Arg153=)
n.1030G>A
c.507G>A (p.Arg169=)
c.657G>A (p.Arg219=)
c.630G>A (p.Arg210=)
ClinVar gnomAD v4
7g.150958169delCA2685607561KCNH2n.1640del
c.807del (p.Thr270ArgfsTer?)
c.459del (p.Thr154ArgfsTer?)
n.1030del
c.507del (p.Thr170ArgfsTer?)
c.657del (p.Thr220ArgfsTer?)
c.630del (p.Thr211ArgfsTer?)
gnomAD v4
7g.150958169C>ACA369862415KCNH2n.1639G>T
c.806G>T (p.Arg269Leu)
c.458G>T (p.Arg153Leu)
n.1029G>T
c.506G>T (p.Arg169Leu)
c.656G>T (p.Arg219Leu)
c.629G>T (p.Arg210Leu)
gnomAD v4
7g.150958169C=CA1752418012KCNH2n.1639G=
c.806G= (p.Arg269=)
c.458G= (p.Arg153=)
n.1029G=
c.506G= (p.Arg169=)
c.656G= (p.Arg219=)
c.629G= (p.Arg210=)
7g.150958169C>GCA369862416KCNH2n.1639G>C
c.806G>C (p.Arg269Pro)
c.458G>C (p.Arg153Pro)
n.1029G>C
c.506G>C (p.Arg169Pro)
c.656G>C (p.Arg219Pro)
c.629G>C (p.Arg210Pro)
gnomAD v4
7g.150958169C>TCA369862417KCNH2n.1639G>A
c.806G>A (p.Arg269Gln)
c.458G>A (p.Arg153Gln)
n.1029G>A
c.506G>A (p.Arg169Gln)
c.656G>A (p.Arg219Gln)
c.629G>A (p.Arg210Gln)
dbSNP gnomAD v4
7g.150958170G>ACA008816KCNH2n.1638C>T
c.805C>T (p.Arg269Trp)
c.457C>T (p.Arg153Trp)
n.1028C>T
c.505C>T (p.Arg169Trp)
c.655C>T (p.Arg219Trp)
c.628C>T (p.Arg210Trp)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150958170G>CCA369862420KCNH2n.1638C>G
c.805C>G (p.Arg269Gly)
c.457C>G (p.Arg153Gly)
n.1028C>G
c.505C>G (p.Arg169Gly)
c.655C>G (p.Arg219Gly)
c.628C>G (p.Arg210Gly)
7g.150958170G=CA1752418016KCNH2n.1638C=
c.805C= (p.Arg269=)
c.457C= (p.Arg153=)
n.1028C=
c.505C= (p.Arg169=)
c.655C= (p.Arg219=)
c.628C= (p.Arg210=)
7g.150958170G>TCA458871944KCNH2n.1638C>A
c.805C>A (p.Arg269=)
c.457C>A (p.Arg153=)
n.1028C>A
c.505C>A (p.Arg169=)
c.655C>A (p.Arg219=)
c.628C>A (p.Arg210=)
gnomAD v4
7g.150958172delCA2573141815KCNH2n.1638del
c.805del (p.Arg269GlyfsTer?)
c.457del (p.Arg153GlyfsTer?)
n.1028del
c.505del (p.Arg169GlyfsTer?)
c.655del (p.Arg219GlyfsTer?)
c.628del (p.Arg210GlyfsTer?)
ClinVar dbSNP
7g.150958171G>ACA458871946KCNH2n.1637C>T
c.804C>T (p.Ala268=)
c.456C>T (p.Ala152=)
n.1027C>T
c.504C>T (p.Ala168=)
c.654C>T (p.Ala218=)
c.627C>T (p.Ala209=)
dbSNP gnomAD v4
7g.150958171G>CCA458871947KCNH2n.1637C>G
c.804C>G (p.Ala268=)
c.456C>G (p.Ala152=)
n.1027C>G
c.504C>G (p.Ala168=)
c.654C>G (p.Ala218=)
c.627C>G (p.Ala209=)
7g.150958171G=CA1752418018KCNH2n.1637C=
c.804C= (p.Ala268=)
c.456C= (p.Ala152=)
n.1027C=
c.504C= (p.Ala168=)
c.654C= (p.Ala218=)
c.627C= (p.Ala209=)
7g.150958171G>TCA458871948KCNH2n.1637C>A
c.804C>A (p.Ala268=)
c.456C>A (p.Ala152=)
n.1027C>A
c.504C>A (p.Ala168=)
c.654C>A (p.Ala218=)
c.627C>A (p.Ala209=)
dbSNP gnomAD v4
7g.150958172G>ACA369862422KCNH2n.1636C>T
c.803C>T (p.Ala268Val)
c.455C>T (p.Ala152Val)
n.1026C>T
c.503C>T (p.Ala168Val)
c.653C>T (p.Ala218Val)
c.626C>T (p.Ala209Val)
ClinVar dbSNP gnomAD v4
7g.150958172G>CCA369862424KCNH2n.1636C>G
c.803C>G (p.Ala268Gly)
c.455C>G (p.Ala152Gly)
n.1026C>G
c.503C>G (p.Ala168Gly)
c.653C>G (p.Ala218Gly)
c.626C>G (p.Ala209Gly)
ClinVar dbSNP gnomAD v4
7g.150958172G=CA1752418022KCNH2n.1636C=
c.803C= (p.Ala268=)
c.455C= (p.Ala152=)
n.1026C=
c.503C= (p.Ala168=)
c.653C= (p.Ala218=)
c.626C= (p.Ala209=)
7g.150958172G>TCA369862426KCNH2n.1636C>A
c.803C>A (p.Ala268Asp)
c.455C>A (p.Ala152Asp)
n.1026C>A
c.503C>A (p.Ala168Asp)
c.653C>A (p.Ala218Asp)
c.626C>A (p.Ala209Asp)
ClinVar dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched