Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.150974747_150974813delCA2580077678KCNH2c.205_271del (p.Leu69SerfsTer25)
c.28_94del (p.Leu10SerfsTer25)
n.428_494del
 ClinVar
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
7g.150974808G>ACA458871909KCNH2c.210C>T (p.His70=)
c.33C>T (p.His11=)
n.433C>T
 dbSNP gnomAD v4
7g.150974808G>CCA369865601KCNH2c.210C>G (p.His70Gln)
c.33C>G (p.His11Gln)
n.433C>G
7g.150974808G=CA1752462340KCNH2c.210C= (p.His70=)
c.33C= (p.His11=)
n.433C=
7g.150974808G>TCA369865599KCNH2c.210C>A (p.His70Gln)
c.33C>A (p.His11Gln)
n.433C>A
7g.150974815_150974830dupCA2573141818KCNH2c.195_210dup (p.Gly71LeufsTer?)
c.18_33dup (p.Gly12LeufsTer?)
n.418_433dup
 ClinVar dbSNP
7g.150974809T>ACA369865603KCNH2c.209A>T (p.His70Leu)
c.32A>T (p.His11Leu)
n.432A>T
7g.150974809T>CCA006229KCNH2c.209A>G (p.His70Arg)
c.32A>G (p.His11Arg)
n.432A>G
 ClinVar dbSNP
7g.150974809T>GCA369865605KCNH2c.209A>C (p.His70Pro)
c.32A>C (p.His11Pro)
n.432A>C
7g.150974809T=CA1752462341KCNH2c.209A= (p.His70=)
c.32A= (p.His11=)
n.432A=
7g.150974810G>ACA369865607KCNH2c.208C>T (p.His70Tyr)
c.31C>T (p.His11Tyr)
n.431C>T
 gnomAD v4
7g.150974810G>CCA369865609KCNH2c.208C>G (p.His70Asp)
c.31C>G (p.His11Asp)
n.431C>G
7g.150974810G=CA1752462349KCNH2c.208C= (p.His70=)
c.31C= (p.His11=)
n.431C=
7g.150974810G>TCA006222KCNH2c.208C>A (p.His70Asn)
c.31C>A (p.His11Asn)
n.431C>A
 ClinVar dbSNP
7g.150974811_150974854delCA2685604706KCNH2c.165_208del (p.Glu58AlafsTer?)
c.-13_31del
n.388_431del
 gnomAD v4
7g.150974811C>ACA458871923KCNH2c.207G>T (p.Leu69=)
c.30G>T (p.Leu10=)
n.430G>T
7g.150974811C>GCA458871922KCNH2c.207G>C (p.Leu69=)
c.30G>C (p.Leu10=)
n.430G>C
7g.150974811C>TCA458871920KCNH2c.207G>A (p.Leu69=)
c.30G>A (p.Leu10=)
n.430G>A
7g.150974812A=CA1752462355KCNH2c.206T= (p.Leu69=)
c.29T= (p.Leu10=)
n.429T=
7g.150974812A>CCA369865612KCNH2c.206T>G (p.Leu69Arg)
c.29T>G (p.Leu10Arg)
n.429T>G
7g.150974812A>GCA006187KCNH2c.206T>C (p.Leu69Pro)
c.29T>C (p.Leu10Pro)
n.429T>C
 ClinVar dbSNP
7g.150974812A>TCA369865614KCNH2c.206T>A (p.Leu69Gln)
c.29T>A (p.Leu10Gln)
n.429T>A
 ClinVar dbSNP
7g.150974813G>ACA458871924KCNH2c.205C>T (p.Leu69=)
c.28C>T (p.Leu10=)
n.428C>T
 gnomAD v4
7g.150974813G>CCA369865616KCNH2c.205C>G (p.Leu69Val)
c.28C>G (p.Leu10Val)
n.428C>G
7g.150974813G>TCA369865618KCNH2c.205C>A (p.Leu69Met)
c.28C>A (p.Leu10Met)
n.428C>A
7g.150974814G>ACA458871930KCNH2c.204C>T (p.Phe68=)
c.27C>T (p.Phe9=)
n.427C>T
 gnomAD v4
7g.150974814G>CCA369865620KCNH2c.204C>G (p.Phe68Leu)
c.27C>G (p.Phe9Leu)
n.427C>G
7g.150974814G>TCA369865622KCNH2c.204C>A (p.Phe68Leu)
c.27C>A (p.Phe9Leu)
n.427C>A
7g.150974815A=CA1752440846KCNH2c.203T= (p.Phe68=)
c.26T= (p.Phe9=)
n.426T=
7g.150974815A>CCA369865625KCNH2c.203T>G (p.Phe68Cys)
c.26T>G (p.Phe9Cys)
n.426T>G
 ClinVar dbSNP
7g.150974815A>GCA369865626KCNH2c.203T>C (p.Phe68Ser)
c.26T>C (p.Phe9Ser)
n.426T>C
7g.150974815A>TCA369865623KCNH2c.203T>A (p.Phe68Tyr)
c.26T>A (p.Phe9Tyr)
n.426T>A
7g.150974816A=CA1752440849KCNH2c.202T= (p.Phe68=)
c.25T= (p.Phe9=)
n.425T=
7g.150974816A>CCA369865629KCNH2c.202T>G (p.Phe68Val)
c.25T>G (p.Phe9Val)
n.425T>G
7g.150974816A>GCA006163KCNH2c.202T>C (p.Phe68Leu)
c.25T>C (p.Phe9Leu)
n.425T>C
 ClinVar dbSNP
7g.150974816A>TCA072439KCNH2c.202T>A (p.Phe68Ile)
c.25T>A (p.Phe9Ile)
n.425T>A
7g.150974817G>ACA458871938KCNH2c.201C>T (p.Asp67=)
c.24C>T (p.Asp8=)
n.424C>T
 gnomAD v4
7g.150974817G>CCA369865631KCNH2c.201C>G (p.Asp67Glu)
c.24C>G (p.Asp8Glu)
n.424C>G
7g.150974817G>TCA369865632KCNH2c.201C>A (p.Asp67Glu)
c.24C>A (p.Asp8Glu)
n.424C>A
7g.150974818T>ACA369865638KCNH2c.200A>T (p.Asp67Val)
c.23A>T (p.Asp8Val)
n.423A>T
7g.150974818T>CCA369865634KCNH2c.200A>G (p.Asp67Gly)
c.23A>G (p.Asp8Gly)
n.423A>G
 ClinVar dbSNP
7g.150974818T>GCA369865636KCNH2c.200A>C (p.Asp67Ala)
c.23A>C (p.Asp8Ala)
n.423A>C
7g.150974818T=CA1752440853KCNH2c.200A= (p.Asp67=)
c.23A= (p.Asp8=)
n.423A=
7g.150974819C>ACA369865640KCNH2c.199G>T (p.Asp67Tyr)
c.22G>T (p.Asp8Tyr)
n.422G>T
7g.150974819C>GCA369865642KCNH2c.199G>C (p.Asp67His)
c.22G>C (p.Asp8His)
n.422G>C
7g.150974819C>TCA369865644KCNH2c.199G>A (p.Asp67Asn)
c.22G>A (p.Asp8Asn)
n.422G>A
7g.150974820G>ACA458871951KCNH2c.198C>T (p.Cys66=)
c.21C>T (p.Cys7=)
n.421C>T
 gnomAD v4
7g.150974820G>CCA369865645KCNH2c.198C>G (p.Cys66Trp)
c.21C>G (p.Cys7Trp)
n.421C>G
7g.150974820G=CA1752440855KCNH2c.198C= (p.Cys66=)
c.21C= (p.Cys7=)
n.421C=
7g.150974820G>TCA369865646KCNH2c.198C>A (p.Cys66Ter)
c.21C>A (p.Cys7Ter)
n.421C>A
 ClinVar dbSNP
7g.150974821C>ACA369865649KCNH2c.197G>T (p.Cys66Phe)
c.20G>T (p.Cys7Phe)
n.420G>T
7g.150974821C=CA1752440858KCNH2c.197G= (p.Cys66=)
c.20G= (p.Cys7=)
n.420G=
7g.150974821C>GCA369865647KCNH2c.197G>C (p.Cys66Ser)
c.20G>C (p.Cys7Ser)
n.420G>C
7g.150974821C>TCA369865648KCNH2c.197G>A (p.Cys66Tyr)
c.20G>A (p.Cys7Tyr)
n.420G>A
 ClinVar dbSNP
7g.150974822A=CA1752440863KCNH2c.196T= (p.Cys66=)
c.19T= (p.Cys7=)
n.419T=
7g.150974822A>CCA006132KCNH2c.196T>G (p.Cys66Gly)
c.19T>G (p.Cys7Gly)
n.419T>G
 ClinVar dbSNP
7g.150974822A>GCA369865654KCNH2c.196T>C (p.Cys66Arg)
c.19T>C (p.Cys7Arg)
n.419T>C
 ClinVar dbSNP
7g.150974822A>TCA369865652KCNH2c.196T>A (p.Cys66Ser)
c.19T>A (p.Cys7Ser)
n.419T>A
7g.150974823G>ACA458871962KCNH2c.195C>T (p.Thr65=)
c.18C>T (p.Thr6=)
n.418C>T
 ClinVar dbSNP
7g.150974823G>CCA458871963KCNH2c.195C>G (p.Thr65=)
c.18C>G (p.Thr6=)
n.418C>G
7g.150974823G>TCA458871968KCNH2c.195C>A (p.Thr65=)
c.18C>A (p.Thr6=)
n.418C>A
7g.150974824G>ACA369865656KCNH2c.194C>T (p.Thr65Ile)
c.17C>T (p.Thr6Ile)
n.417C>T
7g.150974824G>CCA10582468KCNH2c.194C>G (p.Thr65Ser)
c.17C>G (p.Thr6Ser)
n.417C>G
 ClinVar dbSNP gnomAD v4
7g.150974824G=CA1752440879KCNH2c.194C= (p.Thr65=)
c.17C= (p.Thr6=)
n.417C=
7g.150974824G>TCA369865658KCNH2c.194C>A (p.Thr65Asn)
c.17C>A (p.Thr6Asn)
n.417C>A
7g.150974825T>ACA369865660KCNH2c.193A>T (p.Thr65Ser)
c.16A>T (p.Thr6Ser)
n.416A>T
7g.150974825T>CCA369865663KCNH2c.193A>G (p.Thr65Ala)
c.16A>G (p.Thr6Ala)
n.416A>G
 dbSNP
7g.150974825T>GCA006061KCNH2c.193A>C (p.Thr65Pro)
c.16A>C (p.Thr6Pro)
n.416A>C
 ClinVar dbSNP
7g.150974825T=CA1752440883KCNH2c.193A= (p.Thr65=)
c.16A= (p.Thr6=)
n.416A=
7g.150974826G>ACA458871972KCNH2c.192C>T (p.Cys64=)
c.15C>T (p.Cys5=)
n.415C>T
7g.150974826G>CCA006038KCNH2c.192C>G (p.Cys64Trp)
c.15C>G (p.Cys5Trp)
n.415C>G
 ClinVar dbSNP
7g.150974826G=CA1752440909KCNH2c.192C= (p.Cys64=)
c.15C= (p.Cys5=)
n.415C=
7g.150974826G>TCA369865666KCNH2c.192C>A (p.Cys64Ter)
c.15C>A (p.Cys5Ter)
n.415C>A
7g.150974827C>ACA369865668KCNH2c.191G>T (p.Cys64Phe)
c.14G>T (p.Cys5Phe)
n.414G>T
7g.150974827C=CA1752440913KCNH2c.191G= (p.Cys64=)
c.14G= (p.Cys5=)
n.414G=
7g.150974827C>GCA369865670KCNH2c.191G>C (p.Cys64Ser)
c.14G>C (p.Cys5Ser)
n.414G>C
7g.150974827C>TCA006024KCNH2c.191G>A (p.Cys64Tyr)
c.14G>A (p.Cys5Tyr)
n.414G>A
 ClinVar dbSNP
7g.150974828A>CCA369865673KCNH2c.190T>G (p.Cys64Gly)
c.13T>G (p.Cys5Gly)
n.413T>G
7g.150974828A>GCA369865676KCNH2c.190T>C (p.Cys64Arg)
c.13T>C (p.Cys5Arg)
n.413T>C
7g.150974828A>TCA369865674KCNH2c.190T>A (p.Cys64Ser)
c.13T>A (p.Cys5Ser)
n.413T>A
7g.150974829G>ACA029708KCNH2c.189C>T (p.Pro63=)
c.12C>T (p.Pro4=)
n.412C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.150974829G>CCA458871988KCNH2c.189C>G (p.Pro63=)
c.12C>G (p.Pro4=)
n.412C>G
7g.150974829G=CA1752440916KCNH2c.189C= (p.Pro63=)
c.12C= (p.Pro4=)
n.412C=
7g.150974829G>TCA458871986KCNH2c.189C>A (p.Pro63=)
c.12C>A (p.Pro4=)
n.412C>A
7g.150974830G>ACA369865681KCNH2c.188C>T (p.Pro63Leu)
c.11C>T (p.Pro4Leu)
n.411C>T
 ClinVar dbSNP
7g.150974830G>CCA369865678KCNH2c.188C>G (p.Pro63Arg)
c.11C>G (p.Pro4Arg)
n.411C>G
7g.150974830G=CA1752440920KCNH2c.188C= (p.Pro63=)
c.11C= (p.Pro4=)
n.411C=
7g.150974830G>TCA005881KCNH2c.188C>A (p.Pro63His)
c.11C>A (p.Pro4His)
n.411C>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.150974831G>ACA369865682KCNH2c.187C>T (p.Pro63Ser)
c.10C>T (p.Pro4Ser)
n.410C>T
7g.150974831G>CCA369865684KCNH2c.187C>G (p.Pro63Ala)
c.10C>G (p.Pro4Ala)
n.410C>G
7g.150974831G>TCA369865686KCNH2c.187C>A (p.Pro63Thr)
c.10C>A (p.Pro4Thr)
n.410C>A
7g.150974831_150974832insCTCA2512906394KCNH2c.186_187insAG (p.Pro63SerfsTer?)
c.9_10insAG (p.Pro4SerfsTer?)
n.409_410insAG
7g.150974832T>ACA458871998KCNH2c.186A>T (p.Arg62=)
c.9A>T (p.Arg3=)
n.409A>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150974832T>CCA458871999KCNH2c.186A>G (p.Arg62=)
c.9A>G (p.Arg3=)
n.409A>G
 ClinVar
7g.150974832T>GCA458872001KCNH2c.186A>C (p.Arg62=)
c.9A>C (p.Arg3=)
n.409A>C
7g.150974832T=CA1752440926KCNH2c.186A= (p.Arg62=)
c.9A= (p.Arg3=)
n.409A=
7g.150974833C>ACA369865688KCNH2c.185G>T (p.Arg62Leu)
c.8G>T (p.Arg3Leu)
n.408G>T
7g.150974833C=CA1752440932KCNH2c.185G= (p.Arg62=)
c.8G= (p.Arg3=)
n.408G=
7g.150974833C>GCA369865690KCNH2c.185G>C (p.Arg62Pro)
c.8G>C (p.Arg3Pro)
n.408G>C
7g.150974833C>TCA005697KCNH2c.185G>A (p.Arg62Gln)
c.8G>A (p.Arg3Gln)
n.408G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150974834_150974835delCA2519673830KCNH2c.184_185del (p.Arg62ThrfsTer?)
c.7_8del (p.Arg3ThrfsTer?)
n.407_408del
7g.150974834G>ACA369865693KCNH2c.184C>T (p.Arg62Ter)
c.7C>T (p.Arg3Ter)
n.407C>T
 gnomAD v4
7g.150974834G>CCA369865695KCNH2c.184C>G (p.Arg62Gly)
c.7C>G (p.Arg3Gly)
n.407C>G
7g.150974834G=CA1752440937KCNH2c.184C= (p.Arg62=)
c.7C= (p.Arg3=)
n.407C=
7g.150974834G>TCA458872223KCNH2c.184C>A (p.Arg62=)
c.7C>A (p.Arg3=)
n.407C>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.150974835C>ACA369865697KCNH2c.183G>T (p.Gln61His)
c.6G>T (p.Gln2His)
n.406G>T
7g.150974835C>GCA369865698KCNH2c.183G>C (p.Gln61His)
c.6G>C (p.Gln2His)
n.406G>C
7g.150974835C>TCA458872227KCNH2c.183G>A (p.Gln61=)
c.6G>A (p.Gln2=)
n.406G>A
7g.150974835_150974836delinsAGCA2695208670KCNH2c.182_183delinsCT (p.Gln61Pro)
c.5_6delinsCT (p.Gln2Pro)
n.405_406delinsCT
7g.150974836T>ACA369865701KCNH2c.182A>T (p.Gln61Leu)
c.5A>T (p.Gln2Leu)
n.405A>T
7g.150974836T>CCA369865705KCNH2c.182A>G (p.Gln61Arg)
c.5A>G (p.Gln2Arg)
n.405A>G
 ClinVar
7g.150974836T>GCA369865703KCNH2c.182A>C (p.Gln61Pro)
c.5A>C (p.Gln2Pro)
n.405A>C
7g.150974837G>ACA369865707KCNH2c.181C>T (p.Gln61Ter)
c.4C>T (p.Gln2Ter)
n.404C>T
 gnomAD v4
7g.150974837G>CCA369865709KCNH2c.181C>G (p.Gln61Glu)
c.4C>G (p.Gln2Glu)
n.404C>G
 gnomAD v4
7g.150974837G>TCA369865710KCNH2c.181C>A (p.Gln61Lys)
c.4C>A (p.Gln2Lys)
n.404C>A
7g.150974838C>ACA369865712KCNH2c.180G>T (p.Met60Ile)
c.3G>T (p.Met1Ile)
n.403G>T
7g.150974838C>GCA369865714KCNH2c.180G>C (p.Met60Ile)
c.3G>C (p.Met1Ile)
n.403G>C
7g.150974838C>TCA369865716KCNH2c.180G>A (p.Met60Ile)
c.3G>A (p.Met1Ile)
n.403G>A
 ClinVar COSMIC COSMIC
7g.150974839A>CCA369865718KCNH2c.179T>G (p.Met60Arg)
c.2T>G (p.Met1Arg)
n.402T>G
7g.150974839A>GCA369865720KCNH2c.179T>C (p.Met60Thr)
c.2T>C (p.Met1Thr)
n.402T>C
7g.150974839A>TCA369865722KCNH2c.179T>A (p.Met60Lys)
c.2T>A (p.Met1Lys)
n.402T>A
7g.150974840T>ACA369865727KCNH2c.178A>T (p.Met60Leu)
c.1A>T (p.Met1Leu)
n.401A>T
7g.150974840T>CCA369865726KCNH2c.178A>G (p.Met60Val)
c.1A>G (p.Met1Val)
n.401A>G
7g.150974840T>GCA369865724KCNH2c.178A>C (p.Met60Leu)
c.1A>C (p.Met1Leu)
n.401A>C
7g.150974841C>ACA071355KCNH2c.177G>T (p.Val59=)
c.-1G>T (n.-1G>T)
n.400G>T
7g.150974841C=CA1752440944KCNH2c.177G= (p.Val59=)
c.-1G= (n.-1G=)
n.400G=
7g.150974841C>GCA458872259KCNH2c.177G>C (p.Val59=)
c.-1G>C (n.-1G>C)
n.400G>C
7g.150974841C>TCA029471KCNH2c.177G>A (p.Val59=)
c.-1G>A (n.-1G>A)
n.400G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.150974842A>CCA369865731KCNH2c.176T>G (p.Val59Gly)
c.-2T>G (n.-2T>G)
n.399T>G
7g.150974842A>GCA369865732KCNH2c.176T>C (p.Val59Ala)
c.-2T>C (n.-2T>C)
n.399T>C
7g.150974842A>TCA369865734KCNH2c.176T>A (p.Val59Glu)
c.-2T>A (n.-2T>A)
n.399T>A
7g.150974843C>ACA369865737KCNH2c.175G>T (p.Val59Leu)
c.-3G>T (n.-3G>T)
n.398G>T
7g.150974843C>GCA369865738KCNH2c.175G>C (p.Val59Leu)
c.-3G>C (n.-3G>C)
n.398G>C
7g.150974843C>TCA369865739KCNH2c.175G>A (p.Val59Met)
c.-3G>A (n.-3G>A)
n.398G>A
7g.150974844C>ACA369865741KCNH2c.174G>T (p.Glu58Asp)
c.-4G>T (n.-4G>T)
n.397G>T
7g.150974844C=CA1752440948KCNH2c.174G= (p.Glu58=)
c.-4G= (n.-4G=)
n.397G=
7g.150974844C>GCA005364KCNH2c.174G>C (p.Glu58Asp)
c.-4G>C (n.-4G>C)
n.397G>C
 ClinVar dbSNP
7g.150974844C>TCA458872295KCNH2c.174G>A (p.Glu58=)
c.-4G>A (n.-4G>A)
n.397G>A
 gnomAD v4
7g.150974845T>ACA369865742KCNH2c.173A>T (p.Glu58Val)
c.-5A>T (n.-5A>T)
n.396A>T
7g.150974845T>CCA005331KCNH2c.173A>G (p.Glu58Gly)
c.-5A>G (n.-5A>G)
n.396A>G
 ClinVar dbSNP
7g.150974845T>GCA005322KCNH2c.173A>C (p.Glu58Ala)
c.-5A>C (n.-5A>C)
n.396A>C
 ClinVar dbSNP
7g.150974845T=CA1752440965KCNH2c.173A= (p.Glu58=)
c.-5A= (n.-5A=)
n.396A=
7g.150974846C>ACA369865747KCNH2c.172G>T (p.Glu58Ter)
c.-6G>T (n.-6G>T)
n.395G>T
 ClinVar
7g.150974846C=CA1752440975KCNH2c.172G= (p.Glu58=)
c.-6G= (n.-6G=)
n.395G=
7g.150974846C>GCA369865745KCNH2c.172G>C (p.Glu58Gln)
c.-6G>C (n.-6G>C)
n.395G>C
 ClinVar
7g.150974846C>TCA005294KCNH2c.172G>A (p.Glu58Lys)
c.-6G>A (n.-6G>A)
n.395G>A
 ClinVar dbSNP
7g.150974847G>ACA458872310KCNH2c.171C>T (p.Ala57=)
c.-7C>T (n.-7C>T)
n.394C>T
 ClinVar
7g.150974847G>CCA458872311KCNH2c.171C>G (p.Ala57=)
c.-7C>G (n.-7C>G)
n.394C>G
7g.150974847G>TCA458872314KCNH2c.171C>A (p.Ala57=)
c.-7C>A (n.-7C>A)
n.394C>A
7g.150974848G>ACA005221KCNH2c.170C>T (p.Ala57Val)
c.-8C>T (n.-8C>T)
n.393C>T
 ClinVar dbSNP
7g.150974848G>CCA369865751KCNH2c.170C>G (p.Ala57Gly)
c.-8C>G (n.-8C>G)
n.393C>G
7g.150974848G=CA1752440986KCNH2c.170C= (p.Ala57=)
c.-8C= (n.-8C=)
n.393C=
7g.150974848G>TCA369865752KCNH2c.170C>A (p.Ala57Asp)
c.-8C>A (n.-8C>A)
n.393C>A
 gnomAD v4 COSMIC COSMIC
7g.150974849C>ACA369865754KCNH2c.169G>T (p.Ala57Ser)
c.-9G>T (n.-9G>T)
n.392G>T
 ClinVar gnomAD v4
7g.150974849C=CA1752440995KCNH2c.169G= (p.Ala57=)
c.-9G= (n.-9G=)
n.392G=
7g.150974849C>GCA005160KCNH2c.169G>C (p.Ala57Pro)
c.-9G>C (n.-9G>C)
n.392G>C
 ClinVar dbSNP
7g.150974849C>TCA369865757KCNH2c.169G>A (p.Ala57Thr)
c.-9G>A (n.-9G>A)
n.392G>A
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.150974850C>ACA458872324KCNH2c.168G>T (p.Arg56=)
c.-10G>T (n.-10G>T)
n.391G>T
7g.150974850C>GCA458872326KCNH2c.168G>C (p.Arg56=)
c.-10G>C (n.-10G>C)
n.391G>C
7g.150974850C>TCA458872325KCNH2c.168G>A (p.Arg56=)
c.-10G>A (n.-10G>A)
n.391G>A
7g.150974851C>ACA005012KCNH2c.167G>T (p.Arg56Leu)
c.-11G>T (n.-11G>T)
n.390G>T
 ClinVar dbSNP gnomAD v4
7g.150974851C=CA1752441009KCNH2c.167G= (p.Arg56=)
c.-11G= (n.-11G=)
n.390G=
7g.150974851C>GCA369865760KCNH2c.167G>C (p.Arg56Pro)
c.-11G>C (n.-11G>C)
n.390G>C
 ClinVar gnomAD v4
7g.150974851C>TCA005006KCNH2c.167G>A (p.Arg56Gln)
c.-11G>A (n.-11G>A)
n.390G>A
 ClinVar dbSNP
7g.150974852G>ACA369865762KCNH2c.166C>T (p.Arg56Trp)
c.-12C>T (n.-12C>T)
n.389C>T
7g.150974852G>CCA369865764KCNH2c.166C>G (p.Arg56Gly)
c.-12C>G (n.-12C>G)
n.389C>G
 dbSNP
7g.150974852G=CA1752441018KCNH2c.166C= (p.Arg56=)
c.-12C= (n.-12C=)
n.389C=
7g.150974852G>TCA458872333KCNH2c.166C>A (p.Arg56=)
c.-12C>A (n.-12C>A)
n.389C>A
 ClinVar dbSNP gnomAD v4
7g.150974853C>ACA458872335KCNH2c.165G>T (p.Ser55=)
c.-13G>T (n.-13G>T)
n.388G>T
7g.150974853C=CA1752441025KCNH2c.165G= (p.Ser55=)
c.-13G= (n.-13G=)
n.388G=
7g.150974853C>GCA458872337KCNH2c.165G>C (p.Ser55=)
c.-13G>C (n.-13G>C)
n.388G>C
 ClinVar dbSNP gnomAD v4
7g.150974853C>TCA458872339KCNH2c.165G>A (p.Ser55=)
c.-13G>A (n.-13G>A)
n.388G>A
 ClinVar dbSNP
7g.150974854G>ACA004951KCNH2c.164C>T (p.Ser55Leu)
c.-14C>T (n.-14C>T)
n.387C>T
 ClinVar dbSNP gnomAD v4
7g.150974854G>CCA369865767KCNH2c.164C>G (p.Ser55Trp)
c.-14C>G (n.-14C>G)
n.387C>G
 ClinVar
7g.150974854G=CA1752441034KCNH2c.164C= (p.Ser55=)
c.-14C= (n.-14C=)
n.387C=
7g.150974854G>TCA16618417KCNH2c.164C>A (p.Ser55Ter)
c.-14C>A (n.-14C>A)
n.387C>A
 ClinVar dbSNP
7g.150974855A>CCA369865772KCNH2c.163T>G (p.Ser55Ala)
c.-15T>G (n.-15T>G)
n.386T>G
7g.150974855A>GCA369865769KCNH2c.163T>C (p.Ser55Pro)
c.-15T>C (n.-15T>C)
n.386T>C
7g.150974855A>TCA369865771KCNH2c.163T>A (p.Ser55Thr)
c.-15T>A (n.-15T>A)
n.386T>A
7g.150974856G>ACA458872344KCNH2c.162C>T (p.Tyr54=)
c.-16C>T (n.-16C>T)
n.385C>T
 gnomAD v4
7g.150974856G>CCA369865774KCNH2c.162C>G (p.Tyr54Ter)
c.-16C>G (n.-16C>G)
n.385C>G
 ClinVar dbSNP
7g.150974856G=CA1752441042KCNH2c.162C= (p.Tyr54=)
c.-16C= (n.-16C=)
n.385C=
7g.150974856G>TCA369865776KCNH2c.162C>A (p.Tyr54Ter)
c.-16C>A (n.-16C>A)
n.385C>A
 ClinVar dbSNP
7g.150974857T>ACA369865778KCNH2c.161A>T (p.Tyr54Phe)
c.-17A>T (n.-17A>T)
n.384A>T
7g.150974857T>CCA369865779KCNH2c.161A>G (p.Tyr54Cys)
c.-17A>G (n.-17A>G)
n.384A>G
 gnomAD v4
7g.150974857T>GCA369865780KCNH2c.161A>C (p.Tyr54Ser)
c.-17A>C (n.-17A>C)
n.384A>C
7g.150974858A=CA1752441049KCNH2c.160T= (p.Tyr54=)
c.-18T= (n.-18T=)
n.383T=
7g.150974858A>CCA369865781KCNH2c.160T>G (p.Tyr54Asp)
c.-18T>G (n.-18T>G)
n.383T>G
7g.150974858A>GCA004937KCNH2c.160T>C (p.Tyr54His)
c.-18T>C (n.-18T>C)
n.383T>C
 ClinVar dbSNP
7g.150974858A>TCA369865782KCNH2c.160T>A (p.Tyr54Asn)
c.-18T>A (n.-18T>A)
n.383T>A
7g.150974859G>ACA458872359KCNH2c.159C>T (p.Gly53=)
c.-19C>T (n.-19C>T)
n.382C>T
7g.150974859G>CCA458872361KCNH2c.159C>G (p.Gly53=)
c.-19C>G (n.-19C>G)
n.382C>G
 ClinVar
7g.150974859G>TCA458872364KCNH2c.159C>A (p.Gly53=)
c.-19C>A (n.-19C>A)
n.382C>A
 gnomAD v4
7g.150974860C>ACA369865783KCNH2c.158G>T (p.Gly53Val)
c.-20G>T (n.-20G>T)
n.381G>T
7g.150974860C=CA1752441052KCNH2c.158G= (p.Gly53=)
c.-20G= (n.-20G=)
n.381G=
7g.150974860C>GCA369865784KCNH2c.158G>C (p.Gly53Ala)
c.-20G>C (n.-20G>C)
n.381G>C
7g.150974860C>TCA004864KCNH2c.158G>A (p.Gly53Asp)
c.-20G>A (n.-20G>A)
n.381G>A
 ClinVar dbSNP gnomAD v2
7g.150974861C>ACA369865785KCNH2c.157G>T (p.Gly53Cys)
c.-21G>T (n.-21G>T)
n.380G>T
 ClinVar dbSNP
7g.150974861C=CA1752441061KCNH2c.157G= (p.Gly53=)
c.-21G= (n.-21G=)
n.380G=
7g.150974861C>GCA004831KCNH2c.157G>C (p.Gly53Arg)
c.-21G>C (n.-21G>C)
n.380G>C
 ClinVar dbSNP
7g.150974861C>TCA004823KCNH2c.157G>A (p.Gly53Ser)
c.-21G>A (n.-21G>A)
n.380G>A
 ClinVar dbSNP
7g.150974862G>ACA028802KCNH2c.156C>T (p.Cys52=)
c.-22C>T (n.-22C>T)
n.379C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.150974862G>CCA028777KCNH2c.156C>G (p.Cys52Trp)
c.-22C>G (n.-22C>G)
n.379C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.150974862G=CA1752441080KCNH2c.156C= (p.Cys52=)
c.-22C= (n.-22C=)
n.379C=
7g.150974862G>TCA004804KCNH2c.156C>A (p.Cys52Ter)
c.-22C>A (n.-22C>A)
n.379C>A
 ClinVar dbSNP gnomAD v4
7g.150974863C>ACA369865786KCNH2c.155G>T (p.Cys52Phe)
c.-23G>T (n.-23G>T)
n.378G>T
7g.150974863C>GCA369865787KCNH2c.155G>C (p.Cys52Ser)
c.-23G>C (n.-23G>C)
n.378G>C
7g.150974863C>TCA369865788KCNH2c.155G>A (p.Cys52Tyr)
c.-23G>A (n.-23G>A)
n.378G>A
7g.150974863_150974864delinsCACA1752441090KCNH2c.154_155delinsTG (p.Cys52=)
c.-24_-23delinsTG (n.-24_-23delinsTG)
n.377_378delinsTG
7g.150974864delCA004782KCNH2c.154del (p.Cys52AlafsTer8)
c.-24del (n.-24del)
n.377del
 ClinVar dbSNP
7g.150974864A>CCA369865789KCNH2c.154T>G (p.Cys52Gly)
c.-24T>G (n.-24T>G)
n.377T>G
7g.150974864A>GCA369865790KCNH2c.154T>C (p.Cys52Arg)
c.-24T>C (n.-24T>C)
n.377T>C
7g.150974864A>TCA369865791KCNH2c.154T>A (p.Cys52Ser)
c.-24T>A (n.-24T>A)
n.377T>A
7g.150974865C>ACA458872383KCNH2c.153G>T (p.Leu51=)
c.-25G>T (n.-25G>T)
n.376G>T
7g.150974865C=CA1752441101KCNH2c.153G= (p.Leu51=)
c.-25G= (n.-25G=)
n.376G=
7g.150974865C>GCA458872387KCNH2c.153G>C (p.Leu51=)
c.-25G>C (n.-25G>C)
n.376G>C
 gnomAD v4
7g.150974865C>TCA458872388KCNH2c.153G>A (p.Leu51=)
c.-25G>A (n.-25G>A)
n.376G>A
 dbSNP gnomAD v2 gnomAD v4
7g.150974866A>CCA369865793KCNH2c.152T>G (p.Leu51Arg)
c.-26T>G (n.-26T>G)
n.375T>G
7g.150974866A>GCA369865794KCNH2c.152T>C (p.Leu51Pro)
c.-26T>C (n.-26T>C)
n.375T>C
 ClinVar
7g.150974866A>TCA369865792KCNH2c.152T>A (p.Leu51Gln)
c.-26T>A (n.-26T>A)
n.375T>A
7g.150974867G>ACA169090403KCNH2c.151C>T (p.Leu51=)
c.-27C>T (n.-27C>T)
n.374C>T
 dbSNP gnomAD v4
7g.150974867G>CCA369865795KCNH2c.151C>G (p.Leu51Val)
c.-27C>G (n.-27C>G)
n.374C>G
7g.150974867G=CA1752441103KCNH2c.151C= (p.Leu51=)
c.-27C= (n.-27C=)
n.374C=
7g.150974867G>TCA369865796KCNH2c.151C>A (p.Leu51Met)
c.-27C>A (n.-27C>A)
n.374C>A

Number of alleles fetched