Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.150946814_150947018delCA2697557661KCNH2n.4027_4163+68del
c.3194_3330+68del
c.2174_2310+68del
c.2894_3030+68del
c.3044_3180+68del
c.3017_3153+68del
ClinVar
7g.150947007A>CCA369852268KCNH2n.4033T>G
c.3200T>G (p.Leu1067Arg)
c.2180T>G (p.Leu727Arg)
c.2900T>G (p.Leu967Arg)
c.3050T>G (p.Leu1017Arg)
c.3023T>G (p.Leu1008Arg)
7g.150947007A>GCA369852270KCNH2n.4033T>C
c.3200T>C (p.Leu1067Pro)
c.2180T>C (p.Leu727Pro)
c.2900T>C (p.Leu967Pro)
c.3050T>C (p.Leu1017Pro)
c.3023T>C (p.Leu1008Pro)
7g.150947007A>TCA369852271KCNH2n.4033T>A
c.3200T>A (p.Leu1067Gln)
c.2180T>A (p.Leu727Gln)
c.2900T>A (p.Leu967Gln)
c.3050T>A (p.Leu1017Gln)
c.3023T>A (p.Leu1008Gln)
7g.150947007dupCA16042588KCNH2n.4033dup
c.3200dup (p.Gln1068ThrfsTer?)
c.2180dup (p.Gln728ThrfsTer?)
c.2900dup (p.Gln968ThrfsTer?)
c.3050dup (p.Gln1018ThrfsTer?)
c.3023dup (p.Gln1009ThrfsTer?)
ClinVar dbSNP
7g.150947008G>ACA458644740KCNH2n.4032C>T
c.3199C>T (p.Leu1067=)
c.2179C>T (p.Leu727=)
c.2899C>T (p.Leu967=)
c.3049C>T (p.Leu1017=)
c.3022C>T (p.Leu1008=)
7g.150947008G>CCA369852272KCNH2n.4032C>G
c.3199C>G (p.Leu1067Val)
c.2179C>G (p.Leu727Val)
c.2899C>G (p.Leu967Val)
c.3049C>G (p.Leu1017Val)
c.3022C>G (p.Leu1008Val)
7g.150947008G>TCA369852273KCNH2n.4032C>A
c.3199C>A (p.Leu1067Ile)
c.2179C>A (p.Leu727Ile)
c.2899C>A (p.Leu967Ile)
c.3049C>A (p.Leu1017Ile)
c.3022C>A (p.Leu1008Ile)
7g.150947009_150947018delCA2695208695KCNH2n.4023_4032del
c.3190_3199del (p.Leu1064TyrfsTer5)
c.2170_2179del (p.Leu724TyrfsTer5)
c.2890_2899del (p.Leu964TyrfsTer5)
c.3040_3049del (p.Leu1014TyrfsTer5)
c.3013_3022del (p.Leu1005TyrfsTer5)
7g.150947009C>ACA458644741KCNH2n.4031G>T
c.3198G>T (p.Leu1066=)
c.2178G>T (p.Leu726=)
c.2898G>T (p.Leu966=)
c.3048G>T (p.Leu1016=)
c.3021G>T (p.Leu1007=)
dbSNP gnomAD v2 gnomAD v4
7g.150947009C=CA1752427743KCNH2n.4031G=
c.3198G= (p.Leu1066=)
c.2178G= (p.Leu726=)
c.2898G= (p.Leu966=)
c.3048G= (p.Leu1016=)
c.3021G= (p.Leu1007=)
7g.150947009C>GCA458644743KCNH2n.4031G>C
c.3198G>C (p.Leu1066=)
c.2178G>C (p.Leu726=)
c.2898G>C (p.Leu966=)
c.3048G>C (p.Leu1016=)
c.3021G>C (p.Leu1007=)
7g.150947009C>TCA458644742KCNH2n.4031G>A
c.3198G>A (p.Leu1066=)
c.2178G>A (p.Leu726=)
c.2898G>A (p.Leu966=)
c.3048G>A (p.Leu1016=)
c.3021G>A (p.Leu1007=)
7g.150947010A>CCA369852278KCNH2n.4030T>G
c.3197T>G (p.Leu1066Arg)
c.2177T>G (p.Leu726Arg)
c.2897T>G (p.Leu966Arg)
c.3047T>G (p.Leu1016Arg)
c.3020T>G (p.Leu1007Arg)
7g.150947010A>GCA369852276KCNH2n.4030T>C
c.3197T>C (p.Leu1066Pro)
c.2177T>C (p.Leu726Pro)
c.2897T>C (p.Leu966Pro)
c.3047T>C (p.Leu1016Pro)
c.3020T>C (p.Leu1007Pro)
7g.150947010A>TCA369852274KCNH2n.4030T>A
c.3197T>A (p.Leu1066Gln)
c.2177T>A (p.Leu726Gln)
c.2897T>A (p.Leu966Gln)
c.3047T>A (p.Leu1016Gln)
c.3020T>A (p.Leu1007Gln)
7g.150947011G>ACA458644744KCNH2n.4029C>T
c.3196C>T (p.Leu1066=)
c.2176C>T (p.Leu726=)
c.2896C>T (p.Leu966=)
c.3046C>T (p.Leu1016=)
c.3019C>T (p.Leu1007=)
ClinVar dbSNP
7g.150947011G>CCA008093KCNH2n.4029C>G
c.3196C>G (p.Leu1066Val)
c.2176C>G (p.Leu726Val)
c.2896C>G (p.Leu966Val)
c.3046C>G (p.Leu1016Val)
c.3019C>G (p.Leu1007Val)
ClinVar dbSNP
7g.150947011G=CA1752427752KCNH2n.4029C=
c.3196C= (p.Leu1066=)
c.2176C= (p.Leu726=)
c.2896C= (p.Leu966=)
c.3046C= (p.Leu1016=)
c.3019C= (p.Leu1007=)
7g.150947011G>TCA369852280KCNH2n.4029C>A
c.3196C>A (p.Leu1066Met)
c.2176C>A (p.Leu726Met)
c.2896C>A (p.Leu966Met)
c.3046C>A (p.Leu1016Met)
c.3019C>A (p.Leu1007Met)
7g.150947012C>ACA369852282KCNH2n.4028G>T
c.3195G>T (p.Gln1065His)
c.2175G>T (p.Gln725His)
c.2895G>T (p.Gln965His)
c.3045G>T (p.Gln1015His)
c.3018G>T (p.Gln1006His)
7g.150947012C>GCA369852283KCNH2n.4028G>C
c.3195G>C (p.Gln1065His)
c.2175G>C (p.Gln725His)
c.2895G>C (p.Gln965His)
c.3045G>C (p.Gln1015His)
c.3018G>C (p.Gln1006His)
7g.150947012C>TCA458644745KCNH2n.4028G>A
c.3195G>A (p.Gln1065=)
c.2175G>A (p.Gln725=)
c.2895G>A (p.Gln965=)
c.3045G>A (p.Gln1015=)
c.3018G>A (p.Gln1006=)
7g.150947013T>ACA369852285KCNH2n.4027A>T
c.3194A>T (p.Gln1065Leu)
c.2174A>T (p.Gln725Leu)
c.2894A>T (p.Gln965Leu)
c.3044A>T (p.Gln1015Leu)
c.3017A>T (p.Gln1006Leu)
7g.150947013T>CCA369852286KCNH2n.4027A>G
c.3194A>G (p.Gln1065Arg)
c.2174A>G (p.Gln725Arg)
c.2894A>G (p.Gln965Arg)
c.3044A>G (p.Gln1015Arg)
c.3017A>G (p.Gln1006Arg)
ClinVar
7g.150947013T>GCA369852288KCNH2n.4027A>C
c.3194A>C (p.Gln1065Pro)
c.2174A>C (p.Gln725Pro)
c.2894A>C (p.Gln965Pro)
c.3044A>C (p.Gln1015Pro)
c.3017A>C (p.Gln1006Pro)
7g.150947014G>ACA369852293KCNH2n.4026C>T
c.3193C>T (p.Gln1065Ter)
c.2173C>T (p.Gln725Ter)
c.2893C>T (p.Gln965Ter)
c.3043C>T (p.Gln1015Ter)
c.3016C>T (p.Gln1006Ter)
ClinVar dbSNP
7g.150947014G>CCA369852292KCNH2n.4026C>G
c.3193C>G (p.Gln1065Glu)
c.2173C>G (p.Gln725Glu)
c.2893C>G (p.Gln965Glu)
c.3043C>G (p.Gln1015Glu)
c.3016C>G (p.Gln1006Glu)
7g.150947014G=CA1752427762KCNH2n.4026C=
c.3193C= (p.Gln1065=)
c.2173C= (p.Gln725=)
c.2893C= (p.Gln965=)
c.3043C= (p.Gln1015=)
c.3016C= (p.Gln1006=)
7g.150947014G>TCA369852290KCNH2n.4026C>A
c.3193C>A (p.Gln1065Lys)
c.2173C>A (p.Gln725Lys)
c.2893C>A (p.Gln965Lys)
c.3043C>A (p.Gln1015Lys)
c.3016C>A (p.Gln1006Lys)
7g.150947015C>ACA458644746KCNH2n.4025G>T
c.3192G>T (p.Leu1064=)
c.2172G>T (p.Leu724=)
c.2892G>T (p.Leu964=)
c.3042G>T (p.Leu1014=)
c.3015G>T (p.Leu1005=)
7g.150947015C>GCA458644747KCNH2n.4025G>C
c.3192G>C (p.Leu1064=)
c.2172G>C (p.Leu724=)
c.2892G>C (p.Leu964=)
c.3042G>C (p.Leu1014=)
c.3015G>C (p.Leu1005=)
7g.150947015C>TCA458644748KCNH2n.4025G>A
c.3192G>A (p.Leu1064=)
c.2172G>A (p.Leu724=)
c.2892G>A (p.Leu964=)
c.3042G>A (p.Leu1014=)
c.3015G>A (p.Leu1005=)
gnomAD v4
7g.150947016A=CA1752427768KCNH2n.4024T=
c.3191T= (p.Leu1064=)
c.2171T= (p.Leu724=)
c.2891T= (p.Leu964=)
c.3041T= (p.Leu1014=)
c.3014T= (p.Leu1005=)
7g.150947016A>CCA369852295KCNH2n.4024T>G
c.3191T>G (p.Leu1064Arg)
c.2171T>G (p.Leu724Arg)
c.2891T>G (p.Leu964Arg)
c.3041T>G (p.Leu1014Arg)
c.3014T>G (p.Leu1005Arg)
ClinVar dbSNP
7g.150947016A>GCA369852297KCNH2n.4024T>C
c.3191T>C (p.Leu1064Pro)
c.2171T>C (p.Leu724Pro)
c.2891T>C (p.Leu964Pro)
c.3041T>C (p.Leu1014Pro)
c.3014T>C (p.Leu1005Pro)
7g.150947016A>TCA369852298KCNH2n.4024T>A
c.3191T>A (p.Leu1064Gln)
c.2171T>A (p.Leu724Gln)
c.2891T>A (p.Leu964Gln)
c.3041T>A (p.Leu1014Gln)
c.3014T>A (p.Leu1005Gln)
7g.150947017G>ACA458644749KCNH2n.4023C>T
c.3190C>T (p.Leu1064=)
c.2170C>T (p.Leu724=)
c.2890C>T (p.Leu964=)
c.3040C>T (p.Leu1014=)
c.3013C>T (p.Leu1005=)
dbSNP gnomAD v2
7g.150947017G>CCA369852300KCNH2n.4023C>G
c.3190C>G (p.Leu1064Val)
c.2170C>G (p.Leu724Val)
c.2890C>G (p.Leu964Val)
c.3040C>G (p.Leu1014Val)
c.3013C>G (p.Leu1005Val)
7g.150947017G=CA1752427774KCNH2n.4023C=
c.3190C= (p.Leu1064=)
c.2170C= (p.Leu724=)
c.2890C= (p.Leu964=)
c.3040C= (p.Leu1014=)
c.3013C= (p.Leu1005=)
7g.150947017G>TCA369852301KCNH2n.4023C>A
c.3190C>A (p.Leu1064Met)
c.2170C>A (p.Leu724Met)
c.2890C>A (p.Leu964Met)
c.3040C>A (p.Leu1014Met)
c.3013C>A (p.Leu1005Met)
7g.150947018G>ACA037824KCNH2n.4022C>T
c.3189C>T (p.Val1063=)
c.2169C>T (p.Val723=)
c.2889C>T (p.Val963=)
c.3039C>T (p.Val1013=)
c.3012C>T (p.Val1004=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.150947018G>CCA458644750KCNH2n.4022C>G
c.3189C>G (p.Val1063=)
c.2169C>G (p.Val723=)
c.2889C>G (p.Val963=)
c.3039C>G (p.Val1013=)
c.3012C>G (p.Val1004=)
7g.150947018G=CA1752427777KCNH2n.4022C=
c.3189C= (p.Val1063=)
c.2169C= (p.Val723=)
c.2889C= (p.Val963=)
c.3039C= (p.Val1013=)
c.3012C= (p.Val1004=)
7g.150947018G>TCA458644751KCNH2n.4022C>A
c.3189C>A (p.Val1063=)
c.2169C>A (p.Val723=)
c.2889C>A (p.Val963=)
c.3039C>A (p.Val1013=)
c.3012C>A (p.Val1004=)
7g.150947019A>CCA369852303KCNH2n.4021T>G
c.3188T>G (p.Val1063Gly)
c.2168T>G (p.Val723Gly)
c.2888T>G (p.Val963Gly)
c.3038T>G (p.Val1013Gly)
c.3011T>G (p.Val1004Gly)
7g.150947019A>GCA369852305KCNH2n.4021T>C
c.3188T>C (p.Val1063Ala)
c.2168T>C (p.Val723Ala)
c.2888T>C (p.Val963Ala)
c.3038T>C (p.Val1013Ala)
c.3011T>C (p.Val1004Ala)
7g.150947019A>TCA369852304KCNH2n.4021T>A
c.3188T>A (p.Val1063Asp)
c.2168T>A (p.Val723Asp)
c.2888T>A (p.Val963Asp)
c.3038T>A (p.Val1013Asp)
c.3011T>A (p.Val1004Asp)
7g.150947020C>ACA369852307KCNH2n.4020G>T
c.3187G>T (p.Val1063Phe)
c.2167G>T (p.Val723Phe)
c.2887G>T (p.Val963Phe)
c.3037G>T (p.Val1013Phe)
c.3010G>T (p.Val1004Phe)
7g.150947020C=CA1752427781KCNH2n.4020G=
c.3187G= (p.Val1063=)
c.2167G= (p.Val723=)
c.2887G= (p.Val963=)
c.3037G= (p.Val1013=)
c.3010G= (p.Val1004=)

Number of alleles fetched