Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.150974707C=CA1752461714KCNH2c.307+4G= (n.307+4G=)
c.130+4G= (n.130+4G=)
n.530+4G=
7g.150974707C>GCA835213623KCNH2c.307+4G>C (n.307+4G>C)
c.130+4G>C (n.130+4G>C)
n.530+4G>C
 dbSNP gnomAD v3 gnomAD v4
7g.150974707C>TCA036583KCNH2c.307+4G>A (n.307+4G>A)
c.130+4G>A (n.130+4G>A)
n.530+4G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.150974708T=CA1752461720KCNH2c.307+3A= (n.307+3A=)
c.130+3A= (n.130+3A=)
n.530+3A=
7g.150974709A=CA1752461732KCNH2c.307+2T= (n.307+2T=)
c.130+2T= (n.130+2T=)
n.530+2T=
7g.150974709A>CCA369865251KCNH2c.307+2T>G (n.307+2T>G)
c.130+2T>G (n.130+2T>G)
n.530+2T>G
7g.150974709A>GCA369865253KCNH2c.307+2T>C (n.307+2T>C)
c.130+2T>C (n.130+2T>C)
n.530+2T>C
7g.150974709A>TCA204241KCNH2c.307+2T>A (n.307+2T>A)
c.130+2T>A (n.130+2T>A)
n.530+2T>A
 ClinVar dbSNP gnomAD v4
7g.150974709dupCA1752461727KCNH2c.307+2dup (n.307+2dup)
c.130+2dup (n.130+2dup)
n.530+2dup
 dbSNP
7g.150974710C>ACA369865256KCNH2c.307+1G>T (n.307+1G>T)
c.130+1G>T (n.130+1G>T)
n.530+1G>T
7g.150974710C=CA1752461744KCNH2c.307+1G= (n.307+1G=)
c.130+1G= (n.130+1G=)
n.530+1G=
7g.150974710C>GCA369865258KCNH2c.307+1G>C (n.307+1G>C)
c.130+1G>C (n.130+1G>C)
n.530+1G>C
7g.150974710C>TCA369865260KCNH2c.307+1G>A (n.307+1G>A)
c.130+1G>A (n.130+1G>A)
n.530+1G>A
 dbSNP gnomAD v2 gnomAD v4
7g.150974710_150974711delinsAACA658797053KCNH2c.307_307+1delinsTT
c.130_130+1delinsTT
n.530_530+1delinsTT
 ClinVar dbSNP
7g.150974710_150974711delinsCCCA1752461751KCNH2c.307_307+1delinsGG
c.130_130+1delinsGG
n.530_530+1delinsGG
7g.150974711delCA2573141811KCNH2c.307+1del
c.130+1del
n.530+1del
 ClinVar dbSNP gnomAD v4
7g.150974711C>ACA369865262KCNH2c.307G>T (p.Gly103Trp)
c.130G>T (p.Gly44Trp)
n.530G>T
 gnomAD v4
7g.150974711C=CA1752461758KCNH2c.307G= (p.Gly103=)
c.130G= (p.Gly44=)
n.530G=
7g.150974711C>GCA369865264KCNH2c.307G>C (p.Gly103Arg)
c.130G>C (p.Gly44Arg)
n.530G>C
7g.150974711C>TCA369865266KCNH2c.307G>A (p.Gly103Arg)
c.130G>A (p.Gly44Arg)
n.530G>A
 dbSNP gnomAD v2 gnomAD v4
7g.150974712_150974714dupCA2695208642KCNH2c.305_307dup (p.Asp102_Gly103insAsp)
c.128_130dup (p.Asp43_Gly44insAsp)
n.528_530dup
7g.150974712A=CA1752461764KCNH2c.306T= (p.Asp102=)
c.129T= (p.Asp43=)
n.529T=
7g.150974712A>CCA369865268KCNH2c.306T>G (p.Asp102Glu)
c.129T>G (p.Asp43Glu)
n.529T>G
7g.150974712A>GCA169090225KCNH2c.306T>C (p.Asp102=)
c.129T>C (p.Asp43=)
n.529T>C
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150974712A>TCA369865270KCNH2c.306T>A (p.Asp102Glu)
c.129T>A (p.Asp43Glu)
n.529T>A
7g.150974713T>ACA007875KCNH2c.305A>T (p.Asp102Val)
c.128A>T (p.Asp43Val)
n.528A>T
 ClinVar dbSNP
7g.150974713T>CCA369865273KCNH2c.305A>G (p.Asp102Gly)
c.128A>G (p.Asp43Gly)
n.528A>G
 gnomAD v4
7g.150974713T>GCA007867KCNH2c.305A>C (p.Asp102Ala)
c.128A>C (p.Asp43Ala)
n.528A>C
 ClinVar dbSNP
7g.150974713T=CA1752461772KCNH2c.305A= (p.Asp102=)
c.128A= (p.Asp43=)
n.528A=
7g.150974714delCA2695208644KCNH2c.304del (p.Asp102MetfsTer14)
c.127del (p.Asp43MetfsTer14)
n.527del
7g.150974714C>ACA369865275KCNH2c.304G>T (p.Asp102Tyr)
c.127G>T (p.Asp43Tyr)
n.527G>T
 gnomAD v4
7g.150974714C=CA1752461779KCNH2c.304G= (p.Asp102=)
c.127G= (p.Asp43=)
n.527G=
7g.150974714C>GCA369865279KCNH2c.304G>C (p.Asp102His)
c.127G>C (p.Asp43His)
n.527G>C
7g.150974714C>TCA369865277KCNH2c.304G>A (p.Asp102Asn)
c.127G>A (p.Asp43Asn)
n.527G>A
 dbSNP gnomAD v2 gnomAD v4
7g.150974715T>ACA007841KCNH2c.303A>T (p.Lys101Asn)
c.126A>T (p.Lys42Asn)
n.526A>T
 ClinVar dbSNP
7g.150974715T>CCA458871715KCNH2c.303A>G (p.Lys101=)
c.126A>G (p.Lys42=)
n.526A>G
 gnomAD v4
7g.150974715T>GCA369865280KCNH2c.303A>C (p.Lys101Asn)
c.126A>C (p.Lys42Asn)
n.526A>C
7g.150974715T=CA1752461785KCNH2c.303A= (p.Lys101=)
c.126A= (p.Lys42=)
n.526A=
7g.150974716T>ACA369865283KCNH2c.302A>T (p.Lys101Ile)
c.125A>T (p.Lys42Ile)
n.525A>T
7g.150974716T>CCA369865284KCNH2c.302A>G (p.Lys101Arg)
c.125A>G (p.Lys42Arg)
n.525A>G
 ClinVar dbSNP
7g.150974716T>GCA369865285KCNH2c.302A>C (p.Lys101Thr)
c.125A>C (p.Lys42Thr)
n.525A>C
7g.150974717T>ACA007825KCNH2c.301A>T (p.Lys101Ter)
c.124A>T (p.Lys42Ter)
n.524A>T
 ClinVar dbSNP
7g.150974717T>CCA007817KCNH2c.301A>G (p.Lys101Glu)
c.124A>G (p.Lys42Glu)
n.524A>G
 ClinVar dbSNP
7g.150974717T>GCA369865288KCNH2c.301A>C (p.Lys101Gln)
c.124A>C (p.Lys42Gln)
n.524A>C
7g.150974717T=CA1752461797KCNH2c.301A= (p.Lys101=)
c.124A= (p.Lys42=)
n.524A=
7g.150974718C>ACA036266KCNH2c.300G>T (p.Arg100=)
c.123G>T (p.Arg41=)
n.523G>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.150974718C=CA1752461806KCNH2c.300G= (p.Arg100=)
c.123G= (p.Arg41=)
n.523G=
7g.150974718C>GCA458871716KCNH2c.300G>C (p.Arg100=)
c.123G>C (p.Arg41=)
n.523G>C
 gnomAD v4
7g.150974718C>TCA458871717KCNH2c.300G>A (p.Arg100=)
c.123G>A (p.Arg41=)
n.523G>A
 ClinVar
7g.150974719C>ACA369865291KCNH2c.299G>T (p.Arg100Leu)
c.122G>T (p.Arg41Leu)
n.522G>T
 ClinVar dbSNP gnomAD v4
7g.150974719C=CA1752461821KCNH2c.299G= (p.Arg100=)
c.122G= (p.Arg41=)
n.522G=
7g.150974719C>GCA369865293KCNH2c.299G>C (p.Arg100Pro)
c.122G>C (p.Arg41Pro)
n.522G>C
 ClinVar
7g.150974719C>TCA007764KCNH2c.299G>A (p.Arg100Gln)
c.122G>A (p.Arg41Gln)
n.522G>A
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC
7g.150974720G>ACA007747KCNH2c.298C>T (p.Arg100Trp)
c.121C>T (p.Arg41Trp)
n.521C>T
 ClinVar dbSNP gnomAD v4
7g.150974720G>CCA007737KCNH2c.298C>G (p.Arg100Gly)
c.121C>G (p.Arg41Gly)
n.521C>G
 ClinVar dbSNP
7g.150974720G=CA1752461833KCNH2c.298C= (p.Arg100=)
c.121C= (p.Arg41=)
n.521C=
7g.150974720G>TCA036232KCNH2c.298C>A (p.Arg100=)
c.121C>A (p.Arg41=)
n.521C>A
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.150974721G>ACA458871718KCNH2c.297C>T (p.Tyr99=)
c.120C>T (p.Tyr40=)
n.520C>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150974721G>CCA369865298KCNH2c.297C>G (p.Tyr99Ter)
c.120C>G (p.Tyr40Ter)
n.520C>G
7g.150974721G=CA1752461838KCNH2c.297C= (p.Tyr99=)
c.120C= (p.Tyr40=)
n.520C=
7g.150974721G>TCA369865300KCNH2c.297C>A (p.Tyr99Ter)
c.120C>A (p.Tyr40Ter)
n.520C>A
7g.150974722T>ACA369865303KCNH2c.296A>T (p.Tyr99Phe)
c.119A>T (p.Tyr40Phe)
n.519A>T
7g.150974722T>CCA007719KCNH2c.296A>G (p.Tyr99Cys)
c.119A>G (p.Tyr40Cys)
n.519A>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.150974722T>GCA007709KCNH2c.296A>C (p.Tyr99Ser)
c.119A>C (p.Tyr40Ser)
n.519A>C
 ClinVar dbSNP gnomAD v4
7g.150974722T=CA1752461843KCNH2c.296A= (p.Tyr99=)
c.119A= (p.Tyr40=)
n.519A=
7g.150974723A>CCA369865306KCNH2c.295T>G (p.Tyr99Asp)
c.118T>G (p.Tyr40Asp)
n.518T>G
7g.150974723A>GCA369865307KCNH2c.295T>C (p.Tyr99His)
c.118T>C (p.Tyr40His)
n.518T>C
7g.150974723A>TCA369865309KCNH2c.295T>A (p.Tyr99Asn)
c.118T>A (p.Tyr40Asn)
n.518T>A
7g.150974724G>ACA458871719KCNH2c.294C>T (p.Phe98=)
c.117C>T (p.Phe39=)
n.517C>T
 dbSNP gnomAD v2
7g.150974724G>CCA369865311KCNH2c.294C>G (p.Phe98Leu)
c.117C>G (p.Phe39Leu)
n.517C>G
7g.150974724G=CA1752461849KCNH2c.294C= (p.Phe98=)
c.117C= (p.Phe39=)
n.517C=
7g.150974724G>TCA369865313KCNH2c.294C>A (p.Phe98Leu)
c.117C>A (p.Phe39Leu)
n.517C>A
 gnomAD v4
7g.150974725A=CA1752461852KCNH2c.293T= (p.Phe98=)
c.116T= (p.Phe39=)
n.516T=
7g.150974725A>CCA369865315KCNH2c.293T>G (p.Phe98Cys)
c.116T>G (p.Phe39Cys)
n.516T>G
 ClinVar dbSNP
7g.150974725A>GCA369865317KCNH2c.293T>C (p.Phe98Ser)
c.116T>C (p.Phe39Ser)
n.516T>C
7g.150974725A>TCA369865318KCNH2c.293T>A (p.Phe98Tyr)
c.116T>A (p.Phe39Tyr)
n.516T>A
7g.150974725_150974726delinsGCCA2697549693KCNH2c.292_293delinsGC (p.Phe98Ala)
c.115_116delinsGC (p.Phe39Ala)
n.515_516delinsGC
 ClinVar
7g.150974726A>CCA369865322KCNH2c.292T>G (p.Phe98Val)
c.115T>G (p.Phe39Val)
n.515T>G
7g.150974726A>GCA070366KCNH2c.292T>C (p.Phe98Leu)
c.115T>C (p.Phe39Leu)
n.515T>C
7g.150974726A>TCA369865319KCNH2c.292T>A (p.Phe98Ile)
c.115T>A (p.Phe39Ile)
n.515T>A
7g.150974727G>ACA458871722KCNH2c.291C>T (p.Ala97=)
c.114C>T (p.Ala38=)
n.514C>T
 gnomAD v4
7g.150974727G>CCA458871720KCNH2c.291C>G (p.Ala97=)
c.114C>G (p.Ala38=)
n.514C>G
7g.150974727G>TCA458871721KCNH2c.291C>A (p.Ala97=)
c.114C>A (p.Ala38=)
n.514C>A
7g.150974728G>ACA369865324KCNH2c.290C>T (p.Ala97Val)
c.113C>T (p.Ala38Val)
n.513C>T
 gnomAD v4
7g.150974728G>CCA007636KCNH2c.290C>G (p.Ala97Gly)
c.113C>G (p.Ala38Gly)
n.513C>G
 ClinVar dbSNP
7g.150974728G=CA1752461855KCNH2c.290C= (p.Ala97=)
c.113C= (p.Ala38=)
n.513C=
7g.150974728G>TCA369865327KCNH2c.290C>A (p.Ala97Asp)
c.113C>A (p.Ala38Asp)
n.513C>A
 gnomAD v4
7g.150974729C>ACA169090254KCNH2c.289G>T (p.Ala97Ser)
c.112G>T (p.Ala38Ser)
n.512G>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150974729C=CA1752461859KCNH2c.289G= (p.Ala97=)
c.112G= (p.Ala38=)
n.512G=
7g.150974729C>GCA369865329KCNH2c.289G>C (p.Ala97Pro)
c.112G>C (p.Ala38Pro)
n.512G>C
7g.150974729C>TCA369865331KCNH2c.289G>A (p.Ala97Thr)
c.112G>A (p.Ala38Thr)
n.512G>A
 gnomAD v4
7g.150974730G>ACA458871723KCNH2c.288C>T (p.Ile96=)
c.111C>T (p.Ile37=)
n.511C>T
 ClinVar dbSNP gnomAD v4
7g.150974730G>CCA369865333KCNH2c.288C>G (p.Ile96Met)
c.111C>G (p.Ile37Met)
n.511C>G
7g.150974730G>TCA458871724KCNH2c.288C>A (p.Ile96=)
c.111C>A (p.Ile37=)
n.511C>A
 ClinVar dbSNP
7g.150974731A=CA1752461862KCNH2c.287T= (p.Ile96=)
c.110T= (p.Ile37=)
n.510T=
7g.150974731A>CCA369865335KCNH2c.287T>G (p.Ile96Ser)
c.110T>G (p.Ile37Ser)
n.510T>G
7g.150974731A>GCA007567KCNH2c.287T>C (p.Ile96Thr)
c.110T>C (p.Ile37Thr)
n.510T>C
 ClinVar dbSNP
7g.150974731A>TCA369865337KCNH2c.287T>A (p.Ile96Asn)
c.110T>A (p.Ile37Asn)
n.510T>A
7g.150974732T>ACA369865339KCNH2c.286A>T (p.Ile96Phe)
c.109A>T (p.Ile37Phe)
n.509A>T
7g.150974732T>CCA007547KCNH2c.286A>G (p.Ile96Val)
c.109A>G (p.Ile37Val)
n.509A>G
 ClinVar dbSNP
7g.150974732T>GCA369865341KCNH2c.286A>C (p.Ile96Leu)
c.109A>C (p.Ile37Leu)
n.509A>C
7g.150974732T=CA1752461868KCNH2c.286A= (p.Ile96=)
c.109A= (p.Ile37=)
n.509A=
7g.150974733T>ACA369865343KCNH2c.285A>T (p.Glu95Asp)
c.108A>T (p.Glu36Asp)
n.508A>T
7g.150974733T>CCA458871725KCNH2c.285A>G (p.Glu95=)
c.108A>G (p.Glu36=)
n.508A>G
 gnomAD v4
7g.150974733T>GCA369865345KCNH2c.285A>C (p.Glu95Asp)
c.108A>C (p.Glu36Asp)
n.508A>C
7g.150974734T>ACA369865346KCNH2c.284A>T (p.Glu95Val)
c.107A>T (p.Glu36Val)
n.507A>T
7g.150974734T>CCA369865348KCNH2c.284A>G (p.Glu95Gly)
c.107A>G (p.Glu36Gly)
n.507A>G
 gnomAD v4
7g.150974734T>GCA007512KCNH2c.284A>C (p.Glu95Ala)
c.107A>C (p.Glu36Ala)
n.507A>C
 ClinVar dbSNP
7g.150974734T=CA1752461875KCNH2c.284A= (p.Glu95=)
c.107A= (p.Glu36=)
n.507A=
7g.150974735C>ACA369865351KCNH2c.283G>T (p.Glu95Ter)
c.106G>T (p.Glu36Ter)
n.506G>T
7g.150974735C=CA1752461881KCNH2c.283G= (p.Glu95=)
c.106G= (p.Glu36=)
n.506G=
7g.150974735C>GCA369865353KCNH2c.283G>C (p.Glu95Gln)
c.106G>C (p.Glu36Gln)
n.506G>C
7g.150974735C>TCA035006KCNH2c.283G>A (p.Glu95Lys)
c.106G>A (p.Glu36Lys)
n.506G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.150974736C>ACA458871726KCNH2c.282G>T (p.Val94=)
c.105G>T (p.Val35=)
n.505G>T
7g.150974736C>GCA458871727KCNH2c.282G>C (p.Val94=)
c.105G>C (p.Val35=)
n.505G>C
7g.150974736C>TCA458871728KCNH2c.282G>A (p.Val94=)
c.105G>A (p.Val35=)
n.505G>A
7g.150974737delCA2695208649KCNH2c.281del (p.Val94GlyfsTer22)
c.104del (p.Val35GlyfsTer22)
n.504del
7g.150974737A=CA1752461883KCNH2c.281T= (p.Val94=)
c.104T= (p.Val35=)
n.504T=
7g.150974737A>CCA007478KCNH2c.281T>G (p.Val94Gly)
c.104T>G (p.Val35Gly)
n.504T>G
 ClinVar dbSNP
7g.150974737A>GCA369865356KCNH2c.281T>C (p.Val94Ala)
c.104T>C (p.Val35Ala)
n.504T>C
 gnomAD v4
7g.150974737A>TCA369865358KCNH2c.281T>A (p.Val94Glu)
c.104T>A (p.Val35Glu)
n.504T>A
7g.150974738C>ACA369865360KCNH2c.280G>T (p.Val94Leu)
c.103G>T (p.Val35Leu)
n.503G>T
7g.150974738C=CA1752461890KCNH2c.280G= (p.Val94=)
c.103G= (p.Val35=)
n.503G=
7g.150974738C>GCA034895KCNH2c.280G>C (p.Val94Leu)
c.103G>C (p.Val35Leu)
n.503G>C
 ClinVar dbSNP ExAC gnomAD v4
7g.150974738C>TCA072383KCNH2c.280G>A (p.Val94Met)
c.103G>A (p.Val35Met)
n.503G>A
 ClinVar dbSNP
7g.150974739T>ACA369865364KCNH2c.279A>T (p.Lys93Asn)
c.102A>T (p.Lys34Asn)
n.502A>T
7g.150974739T>CCA458871729KCNH2c.279A>G (p.Lys93=)
c.102A>G (p.Lys34=)
n.502A>G
 ClinVar dbSNP
7g.150974739T>GCA369865365KCNH2c.279A>C (p.Lys93Asn)
c.102A>C (p.Lys34Asn)
n.502A>C
7g.150974740T>ACA369865367KCNH2c.278A>T (p.Lys93Ile)
c.101A>T (p.Lys34Ile)
n.501A>T
7g.150974740T>CCA034847KCNH2c.278A>G (p.Lys93Arg)
c.101A>G (p.Lys34Arg)
n.501A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.150974740T>GCA369865370KCNH2c.278A>C (p.Lys93Thr)
c.101A>C (p.Lys34Thr)
n.501A>C
7g.150974740T=CA1752461892KCNH2c.278A= (p.Lys93=)
c.101A= (p.Lys34=)
n.501A=
7g.150974741T>ACA369865372KCNH2c.277A>T (p.Lys93Ter)
c.100A>T (p.Lys34Ter)
n.500A>T
7g.150974741T>CCA369865374KCNH2c.277A>G (p.Lys93Glu)
c.100A>G (p.Lys34Glu)
n.500A>G
7g.150974741T>GCA369865376KCNH2c.277A>C (p.Lys93Gln)
c.100A>C (p.Lys34Gln)
n.500A>C
 dbSNP gnomAD v3 gnomAD v4
7g.150974741T=CA1752461898KCNH2c.277A= (p.Lys93=)
c.100A= (p.Lys34=)
n.500A=
7g.150974742G>ACA034744KCNH2c.276C>T (p.Arg92=)
c.99C>T (p.Arg33=)
n.499C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.150974742G>CCA458871730KCNH2c.276C>G (p.Arg92=)
c.99C>G (p.Arg33=)
n.499C>G
7g.150974742G=CA1752461904KCNH2c.276C= (p.Arg92=)
c.99C= (p.Arg33=)
n.499C=
7g.150974742G>TCA458871731KCNH2c.276C>A (p.Arg92=)
c.99C>A (p.Arg33=)
n.499C>A
 gnomAD v4
7g.150974743C>ACA007325KCNH2c.275G>T (p.Arg92Leu)
c.98G>T (p.Arg33Leu)
n.498G>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.150974743C=CA1752461915KCNH2c.275G= (p.Arg92=)
c.98G= (p.Arg33=)
n.498G=
7g.150974743C>GCA369865378KCNH2c.275G>C (p.Arg92Pro)
c.98G>C (p.Arg33Pro)
n.498G>C
 ClinVar dbSNP
7g.150974743C>TCA369865380KCNH2c.275G>A (p.Arg92His)
c.98G>A (p.Arg33His)
n.498G>A
 gnomAD v4
7g.150974744G>ACA007279KCNH2c.274C>T (p.Arg92Cys)
c.97C>T (p.Arg33Cys)
n.497C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.150974744G>CCA369865383KCNH2c.274C>G (p.Arg92Gly)
c.97C>G (p.Arg33Gly)
n.497C>G
7g.150974744G=CA1752461929KCNH2c.274C= (p.Arg92=)
c.97C= (p.Arg33=)
n.497C=
7g.150974744G>TCA369865385KCNH2c.274C>A (p.Arg92Ser)
c.97C>A (p.Arg33Ser)
n.497C>A
 gnomAD v4
7g.150974745C>ACA072378KCNH2c.273G>T (p.Glu91Asp)
c.96G>T (p.Glu32Asp)
n.496G>T
 ClinVar dbSNP gnomAD v4
7g.150974745C=CA1752461936KCNH2c.273G= (p.Glu91=)
c.96G= (p.Glu32=)
n.496G=
7g.150974745C>GCA369865388KCNH2c.273G>C (p.Glu91Asp)
c.96G>C (p.Glu32Asp)
n.496G>C
 gnomAD v4
7g.150974745C>TCA458871732KCNH2c.273G>A (p.Glu91=)
c.96G>A (p.Glu32=)
n.496G>A
 dbSNP gnomAD v4
7g.150974746T>ACA369865390KCNH2c.272A>T (p.Glu91Val)
c.95A>T (p.Glu32Val)
n.495A>T
 ClinVar dbSNP
7g.150974746T>CCA369865393KCNH2c.272A>G (p.Glu91Gly)
c.95A>G (p.Glu32Gly)
n.495A>G
 dbSNP gnomAD v2 gnomAD v4
7g.150974746T>GCA369865392KCNH2c.272A>C (p.Glu91Ala)
c.95A>C (p.Glu32Ala)
n.495A>C
7g.150974746T=CA1752461941KCNH2c.272A= (p.Glu91=)
c.95A= (p.Glu32=)
n.495A=
7g.150974747C>ACA369865395KCNH2c.271G>T (p.Glu91Ter)
c.94G>T (p.Glu32Ter)
n.494G>T
 gnomAD v4
7g.150974747C>GCA369865396KCNH2c.271G>C (p.Glu91Gln)
c.94G>C (p.Glu32Gln)
n.494G>C
7g.150974747C>TCA369865398KCNH2c.271G>A (p.Glu91Lys)
c.94G>A (p.Glu32Lys)
n.494G>A
 gnomAD v4 COSMIC COSMIC
7g.150974747_150974813delCA2580077678KCNH2c.205_271del (p.Leu69SerfsTer25)
c.28_94del (p.Leu10SerfsTer25)
n.428_494del
 ClinVar
7g.150974748C>ACA369865400KCNH2c.270G>T (p.Glu90Asp)
c.93G>T (p.Glu31Asp)
n.493G>T
 gnomAD v4
7g.150974748C>GCA369865401KCNH2c.270G>C (p.Glu90Asp)
c.93G>C (p.Glu31Asp)
n.493G>C
7g.150974748C>TCA458871736KCNH2c.270G>A (p.Glu90=)
c.93G>A (p.Glu31=)
n.493G>A
 ClinVar dbSNP gnomAD v4
7g.150974749T>ACA369865403KCNH2c.269A>T (p.Glu90Val)
c.92A>T (p.Glu31Val)
n.492A>T
7g.150974749T>CCA369865405KCNH2c.269A>G (p.Glu90Gly)
c.92A>G (p.Glu31Gly)
n.492A>G
 ClinVar
7g.150974749T>GCA369865407KCNH2c.269A>C (p.Glu90Ala)
c.92A>C (p.Glu31Ala)
n.492A>C
7g.150974750C>ACA369865409KCNH2c.268G>T (p.Glu90Ter)
c.91G>T (p.Glu31Ter)
n.491G>T
 ClinVar COSMIC COSMIC
7g.150974750C=CA1752461950KCNH2c.268G= (p.Glu90=)
c.91G= (p.Glu31=)
n.491G=
7g.150974750C>GCA034209KCNH2c.268G>C (p.Glu90Gln)
c.91G>C (p.Glu31Gln)
n.491G>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.150974750C>TCA034184KCNH2c.268G>A (p.Glu90Lys)
c.91G>A (p.Glu31Lys)
n.491G>A
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC
7g.150974751G>ACA458871739KCNH2c.267C>T (p.Ala89=)
c.90C>T (p.Ala30=)
n.490C>T
 ClinVar gnomAD v4
7g.150974751G>CCA034019KCNH2c.267C>G (p.Ala89=)
c.90C>G (p.Ala30=)
n.490C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.150974751G=CA1752461956KCNH2c.267C= (p.Ala89=)
c.90C= (p.Ala30=)
n.490C=
7g.150974751G>TCA458871742KCNH2c.267C>A (p.Ala89=)
c.90C>A (p.Ala30=)
n.490C>A
 gnomAD v4
7g.150974752G>ACA007110KCNH2c.266C>T (p.Ala89Val)
c.89C>T (p.Ala30Val)
n.489C>T
 dbSNP gnomAD v2 gnomAD v4
7g.150974752G>CCA033852KCNH2c.266C>G (p.Ala89Gly)
c.89C>G (p.Ala30Gly)
n.489C>G
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.150974752G=CA1752461964KCNH2c.266C= (p.Ala89=)
c.89C= (p.Ala30=)
n.489C=
7g.150974752G>TCA369865414KCNH2c.266C>A (p.Ala89Asp)
c.89C>A (p.Ala30Asp)
n.489C>A
7g.150974753C>ACA369865417KCNH2c.265G>T (p.Ala89Ser)
c.88G>T (p.Ala30Ser)
n.488G>T
 gnomAD v4
7g.150974753C=CA1752461972KCNH2c.265G= (p.Ala89=)
c.88G= (p.Ala30=)
n.488G=
7g.150974753C>GCA369865419KCNH2c.265G>C (p.Ala89Pro)
c.88G>C (p.Ala30Pro)
n.488G>C
7g.150974753C>TCA369865420KCNH2c.265G>A (p.Ala89Thr)
c.88G>A (p.Ala30Thr)
n.488G>A
 dbSNP gnomAD v4
7g.150974754G>ACA458871747KCNH2c.264C>T (p.Gly88=)
c.87C>T (p.Gly29=)
n.487C>T
7g.150974754G>CCA458871748KCNH2c.264C>G (p.Gly88=)
c.87C>G (p.Gly29=)
n.487C>G
7g.150974754G>TCA458871746KCNH2c.264C>A (p.Gly88=)
c.87C>A (p.Gly29=)
n.487C>A
7g.150974755C>ACA369865421KCNH2c.263G>T (p.Gly88Val)
c.86G>T (p.Gly29Val)
n.486G>T
 gnomAD v4
7g.150974755C>GCA369865423KCNH2c.263G>C (p.Gly88Ala)
c.86G>C (p.Gly29Ala)
n.486G>C
7g.150974755C>TCA369865425KCNH2c.263G>A (p.Gly88Asp)
c.86G>A (p.Gly29Asp)
n.486G>A
7g.150974756C>ACA369865427KCNH2c.262G>T (p.Gly88Cys)
c.85G>T (p.Gly29Cys)
n.485G>T
7g.150974756C>GCA369865428KCNH2c.262G>C (p.Gly88Arg)
c.85G>C (p.Gly29Arg)
n.485G>C
7g.150974756C>TCA369865430KCNH2c.262G>A (p.Gly88Ser)
c.85G>A (p.Gly29Ser)
n.485G>A
 gnomAD v4
7g.150974757C>ACA458871757KCNH2c.261G>T (p.Leu87=)
c.84G>T (p.Leu28=)
n.484G>T
 dbSNP gnomAD v4
7g.150974757C>GCA072405KCNH2c.261G>C (p.Leu87=)
c.84G>C (p.Leu28=)
n.484G>C
7g.150974757C>TCA458871753KCNH2c.261G>A (p.Leu87=)
c.84G>A (p.Leu28=)
n.484G>A
 gnomAD v4
7g.150974758A=CA1752461978KCNH2c.260T= (p.Leu87=)
c.83T= (p.Leu28=)
n.483T=
7g.150974758A>CCA369865432KCNH2c.260T>G (p.Leu87Arg)
c.83T>G (p.Leu28Arg)
n.483T>G
7g.150974758A>GCA007042KCNH2c.260T>C (p.Leu87Pro)
c.83T>C (p.Leu28Pro)
n.483T>C
 ClinVar dbSNP
7g.150974758A>TCA369865434KCNH2c.260T>A (p.Leu87Gln)
c.83T>A (p.Leu28Gln)
n.483T>A
7g.150974759G>ACA458871759KCNH2c.259C>T (p.Leu87=)
c.82C>T (p.Leu28=)
n.482C>T
 gnomAD v4
7g.150974759G>CCA369865438KCNH2c.259C>G (p.Leu87Val)
c.82C>G (p.Leu28Val)
n.482C>G
7g.150974759G>TCA369865437KCNH2c.259C>A (p.Leu87Met)
c.82C>A (p.Leu28Met)
n.482C>A
 gnomAD v4
7g.150974760C>ACA458871760KCNH2c.258G>T (p.Leu86=)
c.81G>T (p.Leu27=)
n.481G>T
 ClinVar dbSNP gnomAD v4
7g.150974760C=CA1752461985KCNH2c.258G= (p.Leu86=)
c.81G= (p.Leu27=)
n.481G=
7g.150974760C>GCA458871762KCNH2c.258G>C (p.Leu86=)
c.81G>C (p.Leu27=)
n.481G>C
 ClinVar dbSNP
7g.150974760C>TCA458871761KCNH2c.258G>A (p.Leu86=)
c.81G>A (p.Leu27=)
n.481G>A
 ClinVar dbSNP gnomAD v4
7g.150974761A=CA1752461988KCNH2c.257T= (p.Leu86=)
c.80T= (p.Leu27=)
n.480T=
7g.150974761A>CCA006969KCNH2c.257T>G (p.Leu86Arg)
c.80T>G (p.Leu27Arg)
n.480T>G
 ClinVar dbSNP
7g.150974761A>GCA006960KCNH2c.257T>C (p.Leu86Pro)
c.80T>C (p.Leu27Pro)
n.480T>C
 ClinVar dbSNP
7g.150974761A>TCA369865442KCNH2c.257T>A (p.Leu86Gln)
c.80T>A (p.Leu27Gln)
n.480T>A
7g.150974762G>ACA033034KCNH2c.256C>T (p.Leu86=)
c.79C>T (p.Leu27=)
n.479C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.150974762G>CCA369865445KCNH2c.256C>G (p.Leu86Val)
c.79C>G (p.Leu27Val)
n.479C>G
7g.150974762G=CA1752461999KCNH2c.256C= (p.Leu86=)
c.79C= (p.Leu27=)
n.479C=
7g.150974762G>TCA369865447KCNH2c.256C>A (p.Leu86Met)
c.79C>A (p.Leu27Met)
n.479C>A
7g.150974763T>ACA458871772KCNH2c.255A>T (p.Ala85=)
c.78A>T (p.Ala26=)
n.478A>T
7g.150974763T>CCA458871774KCNH2c.255A>G (p.Ala85=)
c.78A>G (p.Ala26=)
n.478A>G
7g.150974763T>GCA458871777KCNH2c.255A>C (p.Ala85=)
c.78A>C (p.Ala26=)
n.478A>C
 ClinVar dbSNP
7g.150974763T=CA1752462002KCNH2c.255A= (p.Ala85=)
c.78A= (p.Ala26=)
n.478A=
7g.150974764G>ACA006934KCNH2c.254C>T (p.Ala85Val)
c.77C>T (p.Ala26Val)
n.477C>T
 ClinVar dbSNP
7g.150974764G>CCA369865448KCNH2c.254C>G (p.Ala85Gly)
c.77C>G (p.Ala26Gly)
n.477C>G
7g.150974764G=CA1752462010KCNH2c.254C= (p.Ala85=)
c.77C= (p.Ala26=)
n.477C=
7g.150974764G>TCA369865450KCNH2c.254C>A (p.Ala85Glu)
c.77C>A (p.Ala26Glu)
n.477C>A
7g.150974765C>ACA369865451KCNH2c.253G>T (p.Ala85Ser)
c.76G>T (p.Ala26Ser)
n.476G>T
 gnomAD v4
7g.150974765C=CA1752462023KCNH2c.253G= (p.Ala85=)
c.76G= (p.Ala26=)
n.476G=
7g.150974765C>GCA006926KCNH2c.253G>C (p.Ala85Pro)
c.76G>C (p.Ala26Pro)
n.476G>C
 ClinVar dbSNP gnomAD v4
7g.150974765C>TCA369865453KCNH2c.253G>A (p.Ala85Thr)
c.76G>A (p.Ala26Thr)
n.476G>A
 ClinVar dbSNP gnomAD v4
7g.150974766C>ACA369865459KCNH2c.252G>T (p.Gln84His)
c.75G>T (p.Gln25His)
n.475G>T
 gnomAD v4
7g.150974766C=CA1752462034KCNH2c.252G= (p.Gln84=)
c.75G= (p.Gln25=)
n.475G=
7g.150974766C>GCA369865463KCNH2c.252G>C (p.Gln84His)
c.75G>C (p.Gln25His)
n.475G>C
7g.150974766C>TCA032982KCNH2c.252G>A (p.Gln84=)
c.75G>A (p.Gln25=)
n.475G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.150974773_150974781dupCA305342KCNH2c.244_252dup (p.Gln84_Ala85insIleAlaGln)
c.67_75dup (p.Gln25_Ala26insIleAlaGln)
n.467_475dup
 ClinVar dbSNP
7g.150974773_150974781delCA658761345KCNH2c.244_252del (p.Ile82_Gln84del)
c.67_75del (p.Ile23_Gln25del)
n.467_475del
7g.150974766_150974797delinsCTGCGCGATCTGCGCGGCAGCGCGGCGCTGCGCA1752462036KCNH2c.221_252delinsCGCAGCGCCGCGCTGCCGCGCAGATCGCGCAG (p.Thr74=)
c.44_75delinsCGCAGCGCCGCGCTGCCGCGCAGATCGCGCAG (p.Thr15=)
n.444_475delinsCGCAGCGCCGCGCTGCCGCGCAGATCGCGCAG
7g.150974767T>ACA369865464KCNH2c.251A>T (p.Gln84Leu)
c.74A>T (p.Gln25Leu)
n.474A>T
 gnomAD v4
7g.150974767T>CCA369865466KCNH2c.251A>G (p.Gln84Arg)
c.74A>G (p.Gln25Arg)
n.474A>G
 ClinVar dbSNP gnomAD v4
7g.150974767T>GCA369865468KCNH2c.251A>C (p.Gln84Pro)
c.74A>C (p.Gln25Pro)
n.474A>C
7g.150974767_150974786delinsTGCGCGATCTGCGCGGCAGCCA1752462046KCNH2c.232_251delinsGCTGCCGCGCAGATCGCGCA (p.Ala78=)
c.55_74delinsGCTGCCGCGCAGATCGCGCA (p.Ala19=)
n.455_474delinsGCTGCCGCGCAGATCGCGCA
7g.150974773_150974803delCA658761346KCNH2c.221_251del (p.Thr74ArgfsTer?)
c.44_74del (p.Thr15ArgfsTer?)
n.444_474del
 ClinVar dbSNP
7g.150974768G>ACA369865469KCNH2c.250C>T (p.Gln84Ter)
c.73C>T (p.Gln25Ter)
n.473C>T
 ClinVar gnomAD v4
7g.150974768G>CCA369865471KCNH2c.250C>G (p.Gln84Glu)
c.73C>G (p.Gln25Glu)
n.473C>G
7g.150974768G>TCA369865472KCNH2c.250C>A (p.Gln84Lys)
c.73C>A (p.Gln25Lys)
n.473C>A
 gnomAD v4
7g.150974773_150974789dupCA915945557KCNH2c.234_250dup (p.Gln84LeufsTer?)
c.57_73dup (p.Gln25LeufsTer?)
n.457_473dup
 ClinVar dbSNP
7g.150974771_150974789delCA915945558KCNH2c.232_250del (p.Ala78ArgfsTer?)
c.55_73del (p.Ala19ArgfsTer?)
n.455_473del
 ClinVar dbSNP
7g.150974769C>ACA458871795KCNH2c.249G>T (p.Ala83=)
c.72G>T (p.Ala24=)
n.472G>T
 ClinVar dbSNP
7g.150974769C=CA1752462068KCNH2c.249G= (p.Ala83=)
c.72G= (p.Ala24=)
n.472G=
7g.150974769C>GCA458871794KCNH2c.249G>C (p.Ala83=)
c.72G>C (p.Ala24=)
n.472G>C
 gnomAD v4
7g.150974769C>TCA169090296KCNH2c.249G>A (p.Ala83=)
c.72G>A (p.Ala24=)
n.472G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150974770G>ACA369865475KCNH2c.248C>T (p.Ala83Val)
c.71C>T (p.Ala24Val)
n.471C>T
 gnomAD v4
7g.150974770G>CCA369865478KCNH2c.248C>G (p.Ala83Gly)
c.71C>G (p.Ala24Gly)
n.471C>G
7g.150974770G>TCA369865476KCNH2c.248C>A (p.Ala83Glu)
c.71C>A (p.Ala24Glu)
n.471C>A
 gnomAD v4
7g.150974771C>ACA369865479KCNH2c.247G>T (p.Ala83Ser)
c.70G>T (p.Ala24Ser)
n.470G>T
 ClinVar dbSNP gnomAD v4
7g.150974771C=CA1752462074KCNH2c.247G= (p.Ala83=)
c.70G= (p.Ala24=)
n.470G=
7g.150974771C>GCA006832KCNH2c.247G>C (p.Ala83Pro)
c.70G>C (p.Ala24Pro)
n.470G>C
 dbSNP
7g.150974771C>TCA369865482KCNH2c.247G>A (p.Ala83Thr)
c.70G>A (p.Ala24Thr)
n.470G>A
 gnomAD v4 COSMIC COSMIC
7g.150974772G>ACA458871805KCNH2c.246C>T (p.Ile82=)
c.69C>T (p.Ile23=)
n.469C>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.150974772G>CCA169090305KCNH2c.246C>G (p.Ile82Met)
c.69C>G (p.Ile23Met)
n.469C>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.150974772G=CA1752462089KCNH2c.246C= (p.Ile82=)
c.69C= (p.Ile23=)
n.469C=
7g.150974772G>TCA458871807KCNH2c.246C>A (p.Ile82=)
c.69C>A (p.Ile23=)
n.469C>A
7g.150974773A=CA1752462099KCNH2c.245T= (p.Ile82=)
c.68T= (p.Ile23=)
n.468T=
7g.150974773A>CCA369865487KCNH2c.245T>G (p.Ile82Ser)
c.68T>G (p.Ile23Ser)
n.468T>G
7g.150974773A>GCA369865484KCNH2c.245T>C (p.Ile82Thr)
c.68T>C (p.Ile23Thr)
n.468T>C
 ClinVar dbSNP gnomAD v4
7g.150974773A>TCA369865486KCNH2c.245T>A (p.Ile82Asn)
c.68T>A (p.Ile23Asn)
n.468T>A
7g.150974774T>ACA369865489KCNH2c.244A>T (p.Ile82Phe)
c.67A>T (p.Ile23Phe)
n.467A>T
7g.150974774T>CCA369865491KCNH2c.244A>G (p.Ile82Val)
c.67A>G (p.Ile23Val)
n.467A>G
7g.150974774T>GCA369865492KCNH2c.244A>C (p.Ile82Leu)
c.67A>C (p.Ile23Leu)
n.467A>C
7g.150974775C>ACA369865493KCNH2c.243G>T (p.Gln81His)
c.66G>T (p.Gln22His)
n.466G>T
 dbSNP
7g.150974775C=CA1752462107KCNH2c.243G= (p.Gln81=)
c.66G= (p.Gln22=)
n.466G=
7g.150974775C>GCA006746KCNH2c.243G>C (p.Gln81His)
c.66G>C (p.Gln22His)
n.466G>C
 ClinVar dbSNP gnomAD v4
7g.150974775C>TCA032737KCNH2c.243G>A (p.Gln81=)
c.66G>A (p.Gln22=)
n.466G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.150974776_150974783delCA2695208658KCNH2c.236_243del (p.Ala79AspfsTer?)
c.59_66del (p.Ala20AspfsTer?)
n.459_466del
7g.150974775_150974797delinsCTGCGCGGCAGCGCGGCGCTGCGCA1752462112KCNH2c.221_243delinsCGCAGCGCCGCGCTGCCGCGCAG (p.Thr74=)
c.44_66delinsCGCAGCGCCGCGCTGCCGCGCAG (p.Thr15=)
n.444_466delinsCGCAGCGCCGCGCTGCCGCGCAG
7g.150974776T>ACA369865496KCNH2c.242A>T (p.Gln81Leu)
c.65A>T (p.Gln22Leu)
n.465A>T
7g.150974776T>CCA369865498KCNH2c.242A>G (p.Gln81Arg)
c.65A>G (p.Gln22Arg)
n.465A>G
7g.150974776T>GCA369865499KCNH2c.242A>C (p.Gln81Pro)
c.65A>C (p.Gln22Pro)
n.465A>C
7g.150974776_150974784delinsTGCGCGGCACA1752462117KCNH2c.234_242delinsTGCCGCGCA (p.Ala78=)
c.57_65delinsTGCCGCGCA (p.Ala19=)
n.457_465delinsTGCCGCGCA
7g.150974784_150974805delCA835213821KCNH2c.221_242del (p.Thr74ArgfsTer?)
c.44_65del (p.Thr15ArgfsTer?)
n.444_465del
 ClinVar dbSNP
7g.150974777G>ACA072418KCNH2c.241C>T (p.Gln81Ter)
c.64C>T (p.Gln22Ter)
n.464C>T
7g.150974777G>CCA032701KCNH2c.241C>G (p.Gln81Glu)
c.64C>G (p.Gln22Glu)
n.464C>G
 ClinVar dbSNP ExAC gnomAD v2
7g.150974777G=CA1752462120KCNH2c.241C= (p.Gln81=)
c.64C= (p.Gln22=)
n.464C=
7g.150974777G>TCA369865503KCNH2c.241C>A (p.Gln81Lys)
c.64C>A (p.Gln22Lys)
n.464C>A
7g.150974784_150974791dupCA2695208660KCNH2c.234_241dup (p.Gln81LeufsTer?)
c.57_64dup (p.Gln22LeufsTer?)
n.457_464dup
7g.150974784_150974791delCA10587645KCNH2c.234_241del (p.Ala79AspfsTer?)
c.57_64del (p.Ala20AspfsTer?)
n.457_464del
 ClinVar dbSNP gnomAD v4
7g.150974778C>ACA458871820KCNH2c.240G>T (p.Ala80=)
c.63G>T (p.Ala21=)
n.463G>T
 ClinVar dbSNP
7g.150974778C=CA1752462128KCNH2c.240G= (p.Ala80=)
c.63G= (p.Ala21=)
n.463G=
7g.150974778C>GCA458871821KCNH2c.240G>C (p.Ala80=)
c.63G>C (p.Ala21=)
n.463G>C
 gnomAD v4
7g.150974778C>TCA458871824KCNH2c.240G>A (p.Ala80=)
c.63G>A (p.Ala21=)
n.463G>A
 ClinVar dbSNP gnomAD v4
7g.150974779G>ACA006696KCNH2c.239C>T (p.Ala80Val)
c.62C>T (p.Ala21Val)
n.462C>T
 ClinVar dbSNP gnomAD v4
7g.150974779G>CCA369865505KCNH2c.239C>G (p.Ala80Gly)
c.62C>G (p.Ala21Gly)
n.462C>G
 ClinVar
7g.150974779G=CA1752462133KCNH2c.239C= (p.Ala80=)
c.62C= (p.Ala21=)
n.462C=
7g.150974779G>TCA369865507KCNH2c.239C>A (p.Ala80Glu)
c.62C>A (p.Ala21Glu)
n.462C>A
7g.150974780C>ACA369865509KCNH2c.238G>T (p.Ala80Ser)
c.61G>T (p.Ala21Ser)
n.461G>T
 ClinVar gnomAD v4
7g.150974780C=CA1752462144KCNH2c.238G= (p.Ala80=)
c.61G= (p.Ala21=)
n.461G=
7g.150974780C>GCA006562KCNH2c.238G>C (p.Ala80Pro)
c.61G>C (p.Ala21Pro)
n.461G>C
 ClinVar dbSNP
7g.150974780C>TCA369865511KCNH2c.238G>A (p.Ala80Thr)
c.61G>A (p.Ala21Thr)
n.461G>A
 ClinVar dbSNP gnomAD v4
7g.150974781G>ACA072422KCNH2c.237C>T (p.Ala79=)
c.60C>T (p.Ala20=)
n.460C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150974781G>CCA16612128KCNH2c.237C>G (p.Ala79=)
c.60C>G (p.Ala20=)
n.460C>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.150974781G=CA1752462152KCNH2c.237C= (p.Ala79=)
c.60C= (p.Ala20=)
n.460C=
7g.150974781G>TCA072287KCNH2c.237C>A (p.Ala79=)
c.60C>A (p.Ala20=)
n.460C>A
 ClinVar dbSNP
7g.150974782_150974814delCA2695208662KCNH2c.205_237del (p.Leu69_Ala79del)
c.28_60del (p.Leu10_Ala20del)
n.428_460del
7g.150974782G>ACA369865514KCNH2c.236C>T (p.Ala79Val)
c.59C>T (p.Ala20Val)
n.459C>T
 dbSNP gnomAD v2 gnomAD v4
7g.150974782G>CCA369865515KCNH2c.236C>G (p.Ala79Gly)
c.59C>G (p.Ala20Gly)
n.459C>G
7g.150974782G=CA1752462156KCNH2c.236C= (p.Ala79=)
c.59C= (p.Ala20=)
n.459C=
7g.150974782G>TCA369865517KCNH2c.236C>A (p.Ala79Asp)
c.59C>A (p.Ala20Asp)
n.459C>A
 gnomAD v4
7g.150974783C>ACA369865523KCNH2c.235G>T (p.Ala79Ser)
c.58G>T (p.Ala20Ser)
n.458G>T
 ClinVar dbSNP
7g.150974783C=CA1752462167KCNH2c.235G= (p.Ala79=)
c.58G= (p.Ala20=)
n.458G=
7g.150974783C>GCA006486KCNH2c.235G>C (p.Ala79Pro)
c.58G>C (p.Ala20Pro)
n.458G>C
 ClinVar dbSNP
7g.150974783C>TCA369865519KCNH2c.235G>A (p.Ala79Thr)
c.58G>A (p.Ala20Thr)
n.458G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.150974784A>CCA458871838KCNH2c.234T>G (p.Ala78=)
c.57T>G (p.Ala19=)
n.457T>G
7g.150974784A>GCA458871840KCNH2c.234T>C (p.Ala78=)
c.57T>C (p.Ala19=)
n.457T>C
7g.150974784A>TCA458871841KCNH2c.234T>A (p.Ala78=)
c.57T>A (p.Ala19=)
n.457T>A
7g.150974785G>ACA369865525KCNH2c.233C>T (p.Ala78Val)
c.56C>T (p.Ala19Val)
n.456C>T
 ClinVar dbSNP gnomAD v4
7g.150974785G>CCA369865527KCNH2c.233C>G (p.Ala78Gly)
c.56C>G (p.Ala19Gly)
n.456C>G
7g.150974785G=CA1752462184KCNH2c.233C= (p.Ala78=)
c.56C= (p.Ala19=)
n.456C=
7g.150974785G>TCA369865529KCNH2c.233C>A (p.Ala78Asp)
c.56C>A (p.Ala19Asp)
n.456C>A
 gnomAD v4
7g.150974792_150974805delCA2573141816KCNH2c.220_233del (p.Thr74CysfsTer?)
c.43_56del (p.Thr15CysfsTer?)
n.443_456del
 ClinVar dbSNP
7g.150974786C>ACA369865531KCNH2c.232G>T (p.Ala78Ser)
c.55G>T (p.Ala19Ser)
n.455G>T
7g.150974786C=CA1752462189KCNH2c.232G= (p.Ala78=)
c.55G= (p.Ala19=)
n.455G=
7g.150974786C>GCA006454KCNH2c.232G>C (p.Ala78Pro)
c.55G>C (p.Ala19Pro)
n.455G>C
 ClinVar dbSNP
7g.150974786C>TCA369865533KCNH2c.232G>A (p.Ala78Thr)
c.55G>A (p.Ala19Thr)
n.455G>A
 ClinVar dbSNP gnomAD v4
7g.150974787G>ACA458871851KCNH2c.231C>T (p.Arg77=)
c.54C>T (p.Arg18=)
n.454C>T
7g.150974787G>CCA072240KCNH2c.231C>G (p.Arg77=)
c.54C>G (p.Arg18=)
n.454C>G
7g.150974787G>TCA458871855KCNH2c.231C>A (p.Arg77=)
c.54C>A (p.Arg18=)
n.454C>A
7g.150974788C>ACA369865535KCNH2c.230G>T (p.Arg77Leu)
c.53G>T (p.Arg18Leu)
n.453G>T
 gnomAD v4
7g.150974788C>GCA369865539KCNH2c.230G>C (p.Arg77Pro)
c.53G>C (p.Arg18Pro)
n.453G>C
7g.150974788C>TCA369865537KCNH2c.230G>A (p.Arg77His)
c.53G>A (p.Arg18His)
n.453G>A
 gnomAD v4 COSMIC COSMIC
7g.150974788_150974789delinsACA2580077680KCNH2c.229_230delinsT (p.Arg77SerfsTer?)
c.52_53delinsT (p.Arg18SerfsTer?)
n.452_453delinsT
 ClinVar
7g.150974789G>ACA369865541KCNH2c.229C>T (p.Arg77Cys)
c.52C>T (p.Arg18Cys)
n.452C>T
 gnomAD v4
7g.150974789G>CCA369865542KCNH2c.229C>G (p.Arg77Gly)
c.52C>G (p.Arg18Gly)
n.452C>G
 gnomAD v4
7g.150974789G=CA1752462195KCNH2c.229C= (p.Arg77=)
c.52C= (p.Arg18=)
n.452C=
7g.150974789G>TCA031559KCNH2c.229C>A (p.Arg77Ser)
c.52C>A (p.Arg18Ser)
n.452C>A
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.150974790G>ACA031505KCNH2c.228C>T (p.Arg76=)
c.51C>T (p.Arg17=)
n.451C>T
 dbSNP ExAC
7g.150974790G>CCA072221KCNH2c.228C>G (p.Arg76=)
c.51C>G (p.Arg17=)
n.451C>G
7g.150974790G=CA1752462199KCNH2c.228C= (p.Arg76=)
c.51C= (p.Arg17=)
n.451C=
7g.150974790G>TCA458871862KCNH2c.228C>A (p.Arg76=)
c.51C>A (p.Arg17=)
n.451C>A
 gnomAD v4
7g.150974791C>ACA169090320KCNH2c.227G>T (p.Arg76Leu)
c.50G>T (p.Arg17Leu)
n.450G>T
 ClinVar dbSNP gnomAD v4
7g.150974791C=CA1752462205KCNH2c.227G= (p.Arg76=)
c.50G= (p.Arg17=)
n.450G=
7g.150974791C>GCA369865544KCNH2c.227G>C (p.Arg76Pro)
c.50G>C (p.Arg17Pro)
n.450G>C
7g.150974791C>TCA369865546KCNH2c.227G>A (p.Arg76His)
c.50G>A (p.Arg17His)
n.450G>A
 dbSNP gnomAD v2 gnomAD v4
7g.150974792G>ACA369865547KCNH2c.226C>T (p.Arg76Cys)
c.49C>T (p.Arg17Cys)
n.449C>T
 gnomAD v4
7g.150974792G>CCA369865549KCNH2c.226C>G (p.Arg76Gly)
c.49C>G (p.Arg17Gly)
n.449C>G
7g.150974792G>TCA369865551KCNH2c.226C>A (p.Arg76Ser)
c.49C>A (p.Arg17Ser)
n.449C>A
7g.150974792_150974799delinsACA2695208664KCNH2c.219_226delinsT (p.Thr74AlafsTer?)
c.42_49delinsT (p.Thr15AlafsTer?)
n.442_449delinsT
7g.150974793C>ACA369865553KCNH2c.225G>T (p.Gln75His)
c.48G>T (p.Gln16His)
n.448G>T
 gnomAD v4
7g.150974793C=CA1752462206KCNH2c.225G= (p.Gln75=)
c.48G= (p.Gln16=)
n.448G=
7g.150974793C>GCA369865554KCNH2c.225G>C (p.Gln75His)
c.48G>C (p.Gln16His)
n.448G>C
 dbSNP
7g.150974793C>TCA458871875KCNH2c.225G>A (p.Gln75=)
c.48G>A (p.Gln16=)
n.448G>A
 ClinVar dbSNP gnomAD v4
7g.150974794T>ACA369865556KCNH2c.224A>T (p.Gln75Leu)
c.47A>T (p.Gln16Leu)
n.447A>T
7g.150974794T>CCA369865559KCNH2c.224A>G (p.Gln75Arg)
c.47A>G (p.Gln16Arg)
n.447A>G
 gnomAD v4
7g.150974794T>GCA369865557KCNH2c.224A>C (p.Gln75Pro)
c.47A>C (p.Gln16Pro)
n.447A>C
7g.150974795G>ACA369865561KCNH2c.223C>T (p.Gln75Ter)
c.46C>T (p.Gln16Ter)
n.446C>T
7g.150974795G>CCA369865564KCNH2c.223C>G (p.Gln75Glu)
c.46C>G (p.Gln16Glu)
n.446C>G
 ClinVar dbSNP
7g.150974795G=CA1752462208KCNH2c.223C= (p.Gln75=)
c.46C= (p.Gln16=)
n.446C=
7g.150974795G>TCA369865563KCNH2c.223C>A (p.Gln75Lys)
c.46C>A (p.Gln16Lys)
n.446C>A
7g.150974796C>ACA458871877KCNH2c.222G>T (p.Thr74=)
c.45G>T (p.Thr15=)
n.445G>T
 dbSNP gnomAD v4
7g.150974796C=CA1752462211KCNH2c.222G= (p.Thr74=)
c.45G= (p.Thr15=)
n.445G=
7g.150974796C>GCA458871880KCNH2c.222G>C (p.Thr74=)
c.45G>C (p.Thr15=)
n.445G>C
 ClinVar
7g.150974796C>TCA072424KCNH2c.222G>A (p.Thr74=)
c.45G>A (p.Thr15=)
n.445G>A
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.150974797G>ACA006365KCNH2c.221C>T (p.Thr74Met)
c.44C>T (p.Thr15Met)
n.444C>T
 ClinVar dbSNP
7g.150974797G>CCA006358KCNH2c.221C>G (p.Thr74Arg)
c.44C>G (p.Thr15Arg)
n.444C>G
 ClinVar dbSNP
7g.150974797G=CA1752462227KCNH2c.221C= (p.Thr74=)
c.44C= (p.Thr15=)
n.444C=
7g.150974797G>TCA369865567KCNH2c.221C>A (p.Thr74Lys)
c.44C>A (p.Thr15Lys)
n.444C>A
7g.150974798T>ACA369865570KCNH2c.220A>T (p.Thr74Ser)
c.43A>T (p.Thr15Ser)
n.443A>T
7g.150974798T>CCA369865572KCNH2c.220A>G (p.Thr74Ala)
c.43A>G (p.Thr15Ala)
n.443A>G
 ClinVar dbSNP
7g.150974798T>GCA006352KCNH2c.220A>C (p.Thr74Pro)
c.43A>C (p.Thr15Pro)
n.443A>C
 ClinVar dbSNP
7g.150974798T=CA1752462239KCNH2c.220A= (p.Thr74=)
c.43A= (p.Thr15=)
n.443A=
7g.150974799G>ACA458871888KCNH2c.219C>T (p.Arg73=)
c.42C>T (p.Arg14=)
n.442C>T
7g.150974799G>CCA072429KCNH2c.219C>G (p.Arg73=)
c.42C>G (p.Arg14=)
n.442C>G
7g.150974799G=CA1752462253KCNH2c.219C= (p.Arg73=)
c.42C= (p.Arg14=)
n.442C=
7g.150974799G>TCA031279KCNH2c.219C>A (p.Arg73=)
c.42C>A (p.Arg14=)
n.442C>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.150974800C>ACA369865575KCNH2c.218G>T (p.Arg73Leu)
c.41G>T (p.Arg14Leu)
n.441G>T
7g.150974800C=CA1752462256KCNH2c.218G= (p.Arg73=)
c.41G= (p.Arg14=)
n.441G=
7g.150974800C>GCA369865577KCNH2c.218G>C (p.Arg73Pro)
c.41G>C (p.Arg14Pro)
n.441G>C
 gnomAD v4
7g.150974800C>TCA369865579KCNH2c.218G>A (p.Arg73His)
c.41G>A (p.Arg14His)
n.441G>A
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150974801G>ACA031237KCNH2c.217C>T (p.Arg73Cys)
c.40C>T (p.Arg14Cys)
n.440C>T
 dbSNP ExAC gnomAD v2
7g.150974801G>CCA369865581KCNH2c.217C>G (p.Arg73Gly)
c.40C>G (p.Arg14Gly)
n.440C>G
7g.150974801G=CA1752462259KCNH2c.217C= (p.Arg73=)
c.40C= (p.Arg14=)
n.440C=
7g.150974801G>TCA369865583KCNH2c.217C>A (p.Arg73Ser)
c.40C>A (p.Arg14Ser)
n.440C>A
7g.150974802C>ACA458871895KCNH2c.216G>T (p.Pro72=)
c.39G>T (p.Pro13=)
n.439G>T
7g.150974802C=CA1752462263KCNH2c.216G= (p.Pro72=)
c.39G= (p.Pro13=)
n.439G=
7g.150974802C>GCA458871896KCNH2c.216G>C (p.Pro72=)
c.39G>C (p.Pro13=)
n.439G>C
7g.150974802C>TCA458871897KCNH2c.216G>A (p.Pro72=)
c.39G>A (p.Pro13=)
n.439G>A
 dbSNP gnomAD v4
7g.150974803G>ACA006305KCNH2c.215C>T (p.Pro72Leu)
c.38C>T (p.Pro13Leu)
n.438C>T
 ClinVar dbSNP gnomAD v4
7g.150974803G>CCA006299KCNH2c.215C>G (p.Pro72Arg)
c.38C>G (p.Pro13Arg)
n.438C>G
 ClinVar dbSNP
7g.150974803G=CA1752462274KCNH2c.215C= (p.Pro72=)
c.38C= (p.Pro13=)
n.438C=
7g.150974803G>TCA006293KCNH2c.215C>A (p.Pro72Gln)
c.38C>A (p.Pro13Gln)
n.438C>A
 ClinVar dbSNP
7g.150974803_150974804delinsCCCA2695208667KCNH2c.214_215delinsGG (p.Pro72Gly)
c.37_38delinsGG (p.Pro13Gly)
n.437_438delinsGG
7g.150974804G>ACA006286KCNH2c.214C>T (p.Pro72Ser)
c.37C>T (p.Pro13Ser)
n.437C>T
 ClinVar dbSNP
7g.150974804G>CCA369865587KCNH2c.214C>G (p.Pro72Ala)
c.37C>G (p.Pro13Ala)
n.437C>G
7g.150974804G=CA1752462291KCNH2c.214C= (p.Pro72=)
c.37C= (p.Pro13=)
n.437C=
7g.150974804G>TCA369865588KCNH2c.214C>A (p.Pro72Thr)
c.37C>A (p.Pro13Thr)
n.437C>A
 gnomAD v4
7g.150974805C>ACA030768KCNH2c.213G>T (p.Gly71=)
c.36G>T (p.Gly12=)
n.436G>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
7g.150974805C=CA1752462296KCNH2c.213G= (p.Gly71=)
c.36G= (p.Gly12=)
n.436G=
7g.150974805C>GCA458871905KCNH2c.213G>C (p.Gly71=)
c.36G>C (p.Gly12=)
n.436G>C
7g.150974805C>TCA458871906KCNH2c.213G>A (p.Gly71=)
c.36G>A (p.Gly12=)
n.436G>A
7g.150974806C>ACA369865591KCNH2c.212G>T (p.Gly71Val)
c.35G>T (p.Gly12Val)
n.435G>T
7g.150974806C=CA1752462302KCNH2c.212G= (p.Gly71=)
c.35G= (p.Gly12=)
n.435G=
7g.150974806C>GCA369865592KCNH2c.212G>C (p.Gly71Ala)
c.35G>C (p.Gly12Ala)
n.435G>C
7g.150974806C>TCA10587642KCNH2c.212G>A (p.Gly71Glu)
c.35G>A (p.Gly12Glu)
n.435G>A
 ClinVar dbSNP gnomAD v2
7g.150974807C>ACA369865595KCNH2c.211G>T (p.Gly71Trp)
c.34G>T (p.Gly12Trp)
n.434G>T
 ClinVar dbSNP
7g.150974807C=CA1752462330KCNH2c.211G= (p.Gly71=)
c.34G= (p.Gly12=)
n.434G=
7g.150974807C>GCA006261KCNH2c.211G>C (p.Gly71Arg)
c.34G>C (p.Gly12Arg)
n.434G>C
 ClinVar dbSNP
7g.150974807C>TCA369865597KCNH2c.211G>A (p.Gly71Arg)
c.34G>A (p.Gly12Arg)
n.434G>A
 ClinVar dbSNP gnomAD v2

Number of alleles fetched