Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.150947372_150953685dupCA2580614280KCNH2n.1962-831_3942dup
c.1129-831_3109dup
c.109-831_2089dup
c.829-831_2809dup
c.979-831_2959dup
c.952-831_2932dup
7g.150948918T>ACA369854929KCNH2n.3363A>T
c.2530A>T (p.Met844Leu)
c.1510A>T (p.Met504Leu)
c.2230A>T (p.Met744Leu)
c.2380A>T (p.Met794Leu)
c.2353A>T (p.Met785Leu)
 gnomAD v4
7g.150948918T>CCA032997KCNH2n.3363A>G
c.2530A>G (p.Met844Val)
c.1510A>G (p.Met504Val)
c.2230A>G (p.Met744Val)
c.2380A>G (p.Met794Val)
c.2353A>G (p.Met785Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.150948918T>GCA369854926KCNH2n.3363A>C
c.2530A>C (p.Met844Leu)
c.1510A>C (p.Met504Leu)
c.2230A>C (p.Met744Leu)
c.2380A>C (p.Met794Leu)
c.2353A>C (p.Met785Leu)
7g.150948918T=CA1752431914KCNH2n.3363A=
c.2530A= (p.Met844=)
c.1510A= (p.Met504=)
c.2230A= (p.Met744=)
c.2380A= (p.Met794=)
c.2353A= (p.Met785=)
7g.150948919G>ACA458645140KCNH2n.3362C>T
c.2529C>T (p.Asp843=)
c.1509C>T (p.Asp503=)
c.2229C>T (p.Asp743=)
c.2379C>T (p.Asp793=)
c.2352C>T (p.Asp784=)
 gnomAD v4
7g.150948919G>CCA369854931KCNH2n.3362C>G
c.2529C>G (p.Asp843Glu)
c.1509C>G (p.Asp503Glu)
c.2229C>G (p.Asp743Glu)
c.2379C>G (p.Asp793Glu)
c.2352C>G (p.Asp784Glu)
7g.150948919G>TCA369854933KCNH2n.3362C>A
c.2529C>A (p.Asp843Glu)
c.1509C>A (p.Asp503Glu)
c.2229C>A (p.Asp743Glu)
c.2379C>A (p.Asp793Glu)
c.2352C>A (p.Asp784Glu)
7g.150948920T>ACA032957KCNH2n.3361A>T
c.2528A>T (p.Asp843Val)
c.1508A>T (p.Asp503Val)
c.2228A>T (p.Asp743Val)
c.2378A>T (p.Asp793Val)
c.2351A>T (p.Asp784Val)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.150948920T>CCA369854936KCNH2n.3361A>G
c.2528A>G (p.Asp843Gly)
c.1508A>G (p.Asp503Gly)
c.2228A>G (p.Asp743Gly)
c.2378A>G (p.Asp793Gly)
c.2351A>G (p.Asp784Gly)
 gnomAD v4
7g.150948920T>GCA369854938KCNH2n.3361A>C
c.2528A>C (p.Asp843Ala)
c.1508A>C (p.Asp503Ala)
c.2228A>C (p.Asp743Ala)
c.2378A>C (p.Asp793Ala)
c.2351A>C (p.Asp784Ala)
7g.150948920T=CA1752431918KCNH2n.3361A=
c.2528A= (p.Asp843=)
c.1508A= (p.Asp503=)
c.2228A= (p.Asp743=)
c.2378A= (p.Asp793=)
c.2351A= (p.Asp784=)
7g.150948921C>ACA369854940KCNH2n.3360G>T
c.2527G>T (p.Asp843Tyr)
c.1507G>T (p.Asp503Tyr)
c.2227G>T (p.Asp743Tyr)
c.2377G>T (p.Asp793Tyr)
c.2350G>T (p.Asp784Tyr)
7g.150948921C>GCA369854942KCNH2n.3360G>C
c.2527G>C (p.Asp843His)
c.1507G>C (p.Asp503His)
c.2227G>C (p.Asp743His)
c.2377G>C (p.Asp793His)
c.2350G>C (p.Asp784His)
7g.150948921C>TCA369854944KCNH2n.3360G>A
c.2527G>A (p.Asp843Asn)
c.1507G>A (p.Asp503Asn)
c.2227G>A (p.Asp743Asn)
c.2377G>A (p.Asp793Asn)
c.2350G>A (p.Asp784Asn)
7g.150948922C>ACA458645142KCNH2n.3359G>T
c.2526G>T (p.Leu842=)
c.1506G>T (p.Leu502=)
c.2226G>T (p.Leu742=)
c.2376G>T (p.Leu792=)
c.2349G>T (p.Leu783=)
7g.150948922C>GCA458645143KCNH2n.3359G>C
c.2526G>C (p.Leu842=)
c.1506G>C (p.Leu502=)
c.2226G>C (p.Leu742=)
c.2376G>C (p.Leu792=)
c.2349G>C (p.Leu783=)
7g.150948922C>TCA458645141KCNH2n.3359G>A
c.2526G>A (p.Leu842=)
c.1506G>A (p.Leu502=)
c.2226G>A (p.Leu742=)
c.2376G>A (p.Leu792=)
c.2349G>A (p.Leu783=)
7g.150948923A=CA1752431923KCNH2n.3358T=
c.2525T= (p.Leu842=)
c.1505T= (p.Leu502=)
c.2225T= (p.Leu742=)
c.2375T= (p.Leu792=)
c.2348T= (p.Leu783=)
7g.150948923A>CCA369854946KCNH2n.3358T>G
c.2525T>G (p.Leu842Arg)
c.1505T>G (p.Leu502Arg)
c.2225T>G (p.Leu742Arg)
c.2375T>G (p.Leu792Arg)
c.2348T>G (p.Leu783Arg)
7g.150948923A>GCA369854948KCNH2n.3358T>C
c.2525T>C (p.Leu842Pro)
c.1505T>C (p.Leu502Pro)
c.2225T>C (p.Leu742Pro)
c.2375T>C (p.Leu792Pro)
c.2348T>C (p.Leu783Pro)
 ClinVar dbSNP
7g.150948923A>TCA369854950KCNH2n.3358T>A
c.2525T>A (p.Leu842Gln)
c.1505T>A (p.Leu502Gln)
c.2225T>A (p.Leu742Gln)
c.2375T>A (p.Leu792Gln)
c.2348T>A (p.Leu783Gln)
7g.150948924G>ACA458645144KCNH2n.3357C>T
c.2524C>T (p.Leu842=)
c.1504C>T (p.Leu502=)
c.2224C>T (p.Leu742=)
c.2374C>T (p.Leu792=)
c.2347C>T (p.Leu783=)
 ClinVar
7g.150948924G>CCA369854952KCNH2n.3357C>G
c.2524C>G (p.Leu842Val)
c.1504C>G (p.Leu502Val)
c.2224C>G (p.Leu742Val)
c.2374C>G (p.Leu792Val)
c.2347C>G (p.Leu783Val)
 ClinVar dbSNP gnomAD v4
7g.150948924G>TCA369854953KCNH2n.3357C>A
c.2524C>A (p.Leu842Met)
c.1504C>A (p.Leu502Met)
c.2224C>A (p.Leu742Met)
c.2374C>A (p.Leu792Met)
c.2347C>A (p.Leu783Met)
7g.150948925C>ACA458645145KCNH2n.3356G>T
c.2523G>T (p.Val841=)
c.1503G>T (p.Val501=)
c.2223G>T (p.Val741=)
c.2373G>T (p.Val791=)
c.2346G>T (p.Val782=)
7g.150948925C>GCA458645146KCNH2n.3356G>C
c.2523G>C (p.Val841=)
c.1503G>C (p.Val501=)
c.2223G>C (p.Val741=)
c.2373G>C (p.Val791=)
c.2346G>C (p.Val782=)
 gnomAD v4
7g.150948925C>TCA458645147KCNH2n.3356G>A
c.2523G>A (p.Val841=)
c.1503G>A (p.Val501=)
c.2223G>A (p.Val741=)
c.2373G>A (p.Val791=)
c.2346G>A (p.Val782=)
7g.150948926A=CA1752431924KCNH2n.3355T=
c.2522T= (p.Val841=)
c.1502T= (p.Val501=)
c.2222T= (p.Val741=)
c.2372T= (p.Val791=)
c.2345T= (p.Val782=)
7g.150948926A>CCA369854956KCNH2n.3355T>G
c.2522T>G (p.Val841Gly)
c.1502T>G (p.Val501Gly)
c.2222T>G (p.Val741Gly)
c.2372T>G (p.Val791Gly)
c.2345T>G (p.Val782Gly)
 dbSNP
7g.150948926A>GCA369854958KCNH2n.3355T>C
c.2522T>C (p.Val841Ala)
c.1502T>C (p.Val501Ala)
c.2222T>C (p.Val741Ala)
c.2372T>C (p.Val791Ala)
c.2345T>C (p.Val782Ala)
7g.150948926A>TCA369854954KCNH2n.3355T>A
c.2522T>A (p.Val841Glu)
c.1502T>A (p.Val501Glu)
c.2222T>A (p.Val741Glu)
c.2372T>A (p.Val791Glu)
c.2345T>A (p.Val782Glu)
7g.150948927C>ACA369854960KCNH2n.3354G>T
c.2521G>T (p.Val841Leu)
c.1501G>T (p.Val501Leu)
c.2221G>T (p.Val741Leu)
c.2371G>T (p.Val791Leu)
c.2344G>T (p.Val782Leu)
 ClinVar
7g.150948927C>GCA369854962KCNH2n.3354G>C
c.2521G>C (p.Val841Leu)
c.1501G>C (p.Val501Leu)
c.2221G>C (p.Val741Leu)
c.2371G>C (p.Val791Leu)
c.2344G>C (p.Val782Leu)
7g.150948927C>TCA369854964KCNH2n.3354G>A
c.2521G>A (p.Val841Met)
c.1501G>A (p.Val501Met)
c.2221G>A (p.Val741Met)
c.2371G>A (p.Val791Met)
c.2344G>A (p.Val782Met)
7g.150948928C>ACA369854966KCNH2n.3353G>T
c.2520G>T (p.Glu840Asp)
c.1500G>T (p.Glu500Asp)
c.2220G>T (p.Glu740Asp)
c.2370G>T (p.Glu790Asp)
c.2343G>T (p.Glu781Asp)
7g.150948928C>GCA369854968KCNH2n.3353G>C
c.2520G>C (p.Glu840Asp)
c.1500G>C (p.Glu500Asp)
c.2220G>C (p.Glu740Asp)
c.2370G>C (p.Glu790Asp)
c.2343G>C (p.Glu781Asp)
7g.150948928C>TCA458645148KCNH2n.3353G>A
c.2520G>A (p.Glu840=)
c.1500G>A (p.Glu500=)
c.2220G>A (p.Glu740=)
c.2370G>A (p.Glu790=)
c.2343G>A (p.Glu781=)
7g.150948929T>ACA369854970KCNH2n.3352A>T
c.2519A>T (p.Glu840Val)
c.1499A>T (p.Glu500Val)
c.2219A>T (p.Glu740Val)
c.2369A>T (p.Glu790Val)
c.2342A>T (p.Glu781Val)
 gnomAD v4
7g.150948929T>CCA369854971KCNH2n.3352A>G
c.2519A>G (p.Glu840Gly)
c.1499A>G (p.Glu500Gly)
c.2219A>G (p.Glu740Gly)
c.2369A>G (p.Glu790Gly)
c.2342A>G (p.Glu781Gly)
7g.150948929T>GCA369854973KCNH2n.3352A>C
c.2519A>C (p.Glu840Ala)
c.1499A>C (p.Glu500Ala)
c.2219A>C (p.Glu740Ala)
c.2369A>C (p.Glu790Ala)
c.2342A>C (p.Glu781Ala)
7g.150948930C>ACA369854976KCNH2n.3351G>T
c.2518G>T (p.Glu840Ter)
c.1498G>T (p.Glu500Ter)
c.2218G>T (p.Glu740Ter)
c.2368G>T (p.Glu790Ter)
c.2341G>T (p.Glu781Ter)
7g.150948930C=CA1752431926KCNH2n.3351G=
c.2518G= (p.Glu840=)
c.1498G= (p.Glu500=)
c.2218G= (p.Glu740=)
c.2368G= (p.Glu790=)
c.2341G= (p.Glu781=)
7g.150948930C>GCA032944KCNH2n.3351G>C
c.2518G>C (p.Glu840Gln)
c.1498G>C (p.Glu500Gln)
c.2218G>C (p.Glu740Gln)
c.2368G>C (p.Glu790Gln)
c.2341G>C (p.Glu781Gln)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.150948930C>TCA369854977KCNH2n.3351G>A
c.2518G>A (p.Glu840Lys)
c.1498G>A (p.Glu500Lys)
c.2218G>A (p.Glu740Lys)
c.2368G>A (p.Glu790Lys)
c.2341G>A (p.Glu781Lys)
7g.150948931C>ACA458645149KCNH2n.3350G>T
c.2517G>T (p.Leu839=)
c.1497G>T (p.Leu499=)
c.2217G>T (p.Leu739=)
c.2367G>T (p.Leu789=)
c.2340G>T (p.Leu780=)
7g.150948931C>GCA458645150KCNH2n.3350G>C
c.2517G>C (p.Leu839=)
c.1497G>C (p.Leu499=)
c.2217G>C (p.Leu739=)
c.2367G>C (p.Leu789=)
c.2340G>C (p.Leu780=)
7g.150948931C>TCA458645151KCNH2n.3350G>A
c.2517G>A (p.Leu839=)
c.1497G>A (p.Leu499=)
c.2217G>A (p.Leu739=)
c.2367G>A (p.Leu789=)
c.2340G>A (p.Leu780=)
 ClinVar
7g.150948932A>CCA369854983KCNH2n.3349T>G
c.2516T>G (p.Leu839Arg)
c.1496T>G (p.Leu499Arg)
c.2216T>G (p.Leu739Arg)
c.2366T>G (p.Leu789Arg)
c.2339T>G (p.Leu780Arg)
7g.150948932A>GCA369854981KCNH2n.3349T>C
c.2516T>C (p.Leu839Pro)
c.1496T>C (p.Leu499Pro)
c.2216T>C (p.Leu739Pro)
c.2366T>C (p.Leu789Pro)
c.2339T>C (p.Leu780Pro)
7g.150948932A>TCA369854979KCNH2n.3349T>A
c.2516T>A (p.Leu839Gln)
c.1496T>A (p.Leu499Gln)
c.2216T>A (p.Leu739Gln)
c.2366T>A (p.Leu789Gln)
c.2339T>A (p.Leu780Gln)
7g.150948933G>ACA458645152KCNH2n.3348C>T
c.2515C>T (p.Leu839=)
c.1495C>T (p.Leu499=)
c.2215C>T (p.Leu739=)
c.2365C>T (p.Leu789=)
c.2338C>T (p.Leu780=)
7g.150948933G>CCA369854985KCNH2n.3348C>G
c.2515C>G (p.Leu839Val)
c.1495C>G (p.Leu499Val)
c.2215C>G (p.Leu739Val)
c.2365C>G (p.Leu789Val)
c.2338C>G (p.Leu780Val)
7g.150948933G=CA1752431927KCNH2n.3348C=
c.2515C= (p.Leu839=)
c.1495C= (p.Leu499=)
c.2215C= (p.Leu739=)
c.2365C= (p.Leu789=)
c.2338C= (p.Leu780=)
7g.150948933G>TCA369854987KCNH2n.3348C>A
c.2515C>A (p.Leu839Met)
c.1495C>A (p.Leu499Met)
c.2215C>A (p.Leu739Met)
c.2365C>A (p.Leu789Met)
c.2338C>A (p.Leu780Met)
 ClinVar dbSNP gnomAD v4
7g.150948934C>ACA458645153KCNH2n.3347G>T
c.2514G>T (p.Leu838=)
c.1494G>T (p.Leu498=)
c.2214G>T (p.Leu738=)
c.2364G>T (p.Leu788=)
c.2337G>T (p.Leu779=)
 ClinVar
7g.150948934C>GCA458645155KCNH2n.3347G>C
c.2514G>C (p.Leu838=)
c.1494G>C (p.Leu498=)
c.2214G>C (p.Leu738=)
c.2364G>C (p.Leu788=)
c.2337G>C (p.Leu779=)
7g.150948934C>TCA458645154KCNH2n.3347G>A
c.2514G>A (p.Leu838=)
c.1494G>A (p.Leu498=)
c.2214G>A (p.Leu738=)
c.2364G>A (p.Leu788=)
c.2337G>A (p.Leu779=)
7g.150948935A>CCA369854989KCNH2n.3346T>G
c.2513T>G (p.Leu838Arg)
c.1493T>G (p.Leu498Arg)
c.2213T>G (p.Leu738Arg)
c.2363T>G (p.Leu788Arg)
c.2336T>G (p.Leu779Arg)
7g.150948935A>GCA369854991KCNH2n.3346T>C
c.2513T>C (p.Leu838Pro)
c.1493T>C (p.Leu498Pro)
c.2213T>C (p.Leu738Pro)
c.2363T>C (p.Leu788Pro)
c.2336T>C (p.Leu779Pro)
7g.150948935A>TCA369854993KCNH2n.3346T>A
c.2513T>A (p.Leu838Gln)
c.1493T>A (p.Leu498Gln)
c.2213T>A (p.Leu738Gln)
c.2363T>A (p.Leu788Gln)
c.2336T>A (p.Leu779Gln)
7g.150948936G>ACA458645156KCNH2n.3345C>T
c.2512C>T (p.Leu838=)
c.1492C>T (p.Leu498=)
c.2212C>T (p.Leu738=)
c.2362C>T (p.Leu788=)
c.2335C>T (p.Leu779=)
7g.150948936G>CCA369854995KCNH2n.3345C>G
c.2512C>G (p.Leu838Val)
c.1492C>G (p.Leu498Val)
c.2212C>G (p.Leu738Val)
c.2362C>G (p.Leu788Val)
c.2335C>G (p.Leu779Val)
7g.150948936G>TCA369854997KCNH2n.3345C>A
c.2512C>A (p.Leu838Met)
c.1492C>A (p.Leu498Met)
c.2212C>A (p.Leu738Met)
c.2362C>A (p.Leu788Met)
c.2335C>A (p.Leu779Met)
7g.150948937G>ACA458645158KCNH2n.3344C>T
c.2511C>T (p.Asp837=)
c.1491C>T (p.Asp497=)
c.2211C>T (p.Asp737=)
c.2361C>T (p.Asp787=)
c.2334C>T (p.Asp778=)
 dbSNP gnomAD v2 gnomAD v4
7g.150948937G>CCA369854999KCNH2n.3344C>G
c.2511C>G (p.Asp837Glu)
c.1491C>G (p.Asp497Glu)
c.2211C>G (p.Asp737Glu)
c.2361C>G (p.Asp787Glu)
c.2334C>G (p.Asp778Glu)
7g.150948937G=CA1752431933KCNH2n.3344C=
c.2511C= (p.Asp837=)
c.1491C= (p.Asp497=)
c.2211C= (p.Asp737=)
c.2361C= (p.Asp787=)
c.2334C= (p.Asp778=)
7g.150948937G>TCA369855001KCNH2n.3344C>A
c.2511C>A (p.Asp837Glu)
c.1491C>A (p.Asp497Glu)
c.2211C>A (p.Asp737Glu)
c.2361C>A (p.Asp787Glu)
c.2334C>A (p.Asp778Glu)
7g.150948938T>ACA369855003KCNH2n.3343A>T
c.2510A>T (p.Asp837Val)
c.1490A>T (p.Asp497Val)
c.2210A>T (p.Asp737Val)
c.2360A>T (p.Asp787Val)
c.2333A>T (p.Asp778Val)
7g.150948938T>CCA006888KCNH2n.3343A>G
c.2510A>G (p.Asp837Gly)
c.1490A>G (p.Asp497Gly)
c.2210A>G (p.Asp737Gly)
c.2360A>G (p.Asp787Gly)
c.2333A>G (p.Asp778Gly)
 ClinVar dbSNP gnomAD v4
7g.150948938T>GCA369855005KCNH2n.3343A>C
c.2510A>C (p.Asp837Ala)
c.1490A>C (p.Asp497Ala)
c.2210A>C (p.Asp737Ala)
c.2360A>C (p.Asp787Ala)
c.2333A>C (p.Asp778Ala)
7g.150948938T=CA1752431937KCNH2n.3343A=
c.2510A= (p.Asp837=)
c.1490A= (p.Asp497=)
c.2210A= (p.Asp737=)
c.2360A= (p.Asp787=)
c.2333A= (p.Asp778=)
7g.150948939C>ACA006879KCNH2n.3342G>T
c.2509G>T (p.Asp837Tyr)
c.1489G>T (p.Asp497Tyr)
c.2209G>T (p.Asp737Tyr)
c.2359G>T (p.Asp787Tyr)
c.2332G>T (p.Asp778Tyr)
 ClinVar dbSNP
7g.150948939C=CA1752431942KCNH2n.3342G=
c.2509G= (p.Asp837=)
c.1489G= (p.Asp497=)
c.2209G= (p.Asp737=)
c.2359G= (p.Asp787=)
c.2332G= (p.Asp778=)
7g.150948939C>GCA369855009KCNH2n.3342G>C
c.2509G>C (p.Asp837His)
c.1489G>C (p.Asp497His)
c.2209G>C (p.Asp737His)
c.2359G>C (p.Asp787His)
c.2332G>C (p.Asp778His)
 dbSNP
7g.150948939C>TCA006870KCNH2n.3342G>A
c.2509G>A (p.Asp837Asn)
c.1489G>A (p.Asp497Asn)
c.2209G>A (p.Asp737Asn)
c.2359G>A (p.Asp787Asn)
c.2332G>A (p.Asp778Asn)
 ClinVar dbSNP
7g.150948940G>ACA169074781KCNH2n.3341C>T
c.2508C>T (p.Asp836=)
c.1488C>T (p.Asp496=)
c.2208C>T (p.Asp736=)
c.2358C>T (p.Asp786=)
c.2331C>T (p.Asp777=)
 ClinVar dbSNP gnomAD v4
7g.150948940G>CCA369855012KCNH2n.3341C>G
c.2508C>G (p.Asp836Glu)
c.1488C>G (p.Asp496Glu)
c.2208C>G (p.Asp736Glu)
c.2358C>G (p.Asp786Glu)
c.2331C>G (p.Asp777Glu)
 ClinVar
7g.150948940G=CA1752431947KCNH2n.3341C=
c.2508C= (p.Asp836=)
c.1488C= (p.Asp496=)
c.2208C= (p.Asp736=)
c.2358C= (p.Asp786=)
c.2331C= (p.Asp777=)
7g.150948940G>TCA369855014KCNH2n.3341C>A
c.2508C>A (p.Asp836Glu)
c.1488C>A (p.Asp496Glu)
c.2208C>A (p.Asp736Glu)
c.2358C>A (p.Asp786Glu)
c.2331C>A (p.Asp777Glu)
7g.150948941T>ACA369855017KCNH2n.3340A>T
c.2507A>T (p.Asp836Val)
c.1487A>T (p.Asp496Val)
c.2207A>T (p.Asp736Val)
c.2357A>T (p.Asp786Val)
c.2330A>T (p.Asp777Val)
7g.150948941T>CCA369855021KCNH2n.3340A>G
c.2507A>G (p.Asp836Gly)
c.1487A>G (p.Asp496Gly)
c.2207A>G (p.Asp736Gly)
c.2357A>G (p.Asp786Gly)
c.2330A>G (p.Asp777Gly)
7g.150948941T>GCA369855019KCNH2n.3340A>C
c.2507A>C (p.Asp836Ala)
c.1487A>C (p.Asp496Ala)
c.2207A>C (p.Asp736Ala)
c.2357A>C (p.Asp786Ala)
c.2330A>C (p.Asp777Ala)
7g.150948942C>ACA369855023KCNH2n.3339G>T
c.2506G>T (p.Asp836Tyr)
c.1486G>T (p.Asp496Tyr)
c.2206G>T (p.Asp736Tyr)
c.2356G>T (p.Asp786Tyr)
c.2329G>T (p.Asp777Tyr)
7g.150948942C>GCA369855024KCNH2n.3339G>C
c.2506G>C (p.Asp836His)
c.1486G>C (p.Asp496His)
c.2206G>C (p.Asp736His)
c.2356G>C (p.Asp786His)
c.2329G>C (p.Asp777His)
7g.150948942C>TCA369855026KCNH2n.3339G>A
c.2506G>A (p.Asp836Asn)
c.1486G>A (p.Asp496Asn)
c.2206G>A (p.Asp736Asn)
c.2356G>A (p.Asp786Asn)
c.2329G>A (p.Asp777Asn)
7g.150948944_150948980delCA645565632KCNH2n.3303_3339del
c.2470_2506del (p.Ala824ThrfsTer?)
c.1450_1486del (p.Ala484ThrfsTer?)
c.2170_2206del (p.Ala724ThrfsTer?)
c.2320_2356del (p.Ala774ThrfsTer?)
c.2293_2329del (p.Ala765ThrfsTer?)
 COSMIC COSMIC
7g.150948943C>ACA458645159KCNH2n.3338G>T
c.2505G>T (p.Arg835=)
c.1485G>T (p.Arg495=)
c.2205G>T (p.Arg735=)
c.2355G>T (p.Arg785=)
c.2328G>T (p.Arg776=)
7g.150948943C>GCA458645160KCNH2n.3338G>C
c.2505G>C (p.Arg835=)
c.1485G>C (p.Arg495=)
c.2205G>C (p.Arg735=)
c.2355G>C (p.Arg785=)
c.2328G>C (p.Arg776=)
7g.150948943C>TCA458645161KCNH2n.3338G>A
c.2505G>A (p.Arg835=)
c.1485G>A (p.Arg495=)
c.2205G>A (p.Arg735=)
c.2355G>A (p.Arg785=)
c.2328G>A (p.Arg776=)
7g.150948944C>ACA369855028KCNH2n.3337G>T
c.2504G>T (p.Arg835Leu)
c.1484G>T (p.Arg495Leu)
c.2204G>T (p.Arg735Leu)
c.2354G>T (p.Arg785Leu)
c.2327G>T (p.Arg776Leu)
7g.150948944C=CA1752431953KCNH2n.3337G=
c.2504G= (p.Arg835=)
c.1484G= (p.Arg495=)
c.2204G= (p.Arg735=)
c.2354G= (p.Arg785=)
c.2327G= (p.Arg776=)
7g.150948944C>GCA369855030KCNH2n.3337G>C
c.2504G>C (p.Arg835Pro)
c.1484G>C (p.Arg495Pro)
c.2204G>C (p.Arg735Pro)
c.2354G>C (p.Arg785Pro)
c.2327G>C (p.Arg776Pro)
7g.150948944C>TCA006860KCNH2n.3337G>A
c.2504G>A (p.Arg835Gln)
c.1484G>A (p.Arg495Gln)
c.2204G>A (p.Arg735Gln)
c.2354G>A (p.Arg785Gln)
c.2327G>A (p.Arg776Gln)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150948945delCA2695208826KCNH2n.3336del
c.2503del (p.Arg835GlyfsTer?)
c.1483del (p.Arg495GlyfsTer?)
c.2203del (p.Arg735GlyfsTer?)
c.2353del (p.Arg785GlyfsTer?)
c.2326del (p.Arg776GlyfsTer?)
7g.150948945G>ACA006850KCNH2n.3336C>T
c.2503C>T (p.Arg835Trp)
c.1483C>T (p.Arg495Trp)
c.2203C>T (p.Arg735Trp)
c.2353C>T (p.Arg785Trp)
c.2326C>T (p.Arg776Trp)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150948945G>CCA369855034KCNH2n.3336C>G
c.2503C>G (p.Arg835Gly)
c.1483C>G (p.Arg495Gly)
c.2203C>G (p.Arg735Gly)
c.2353C>G (p.Arg785Gly)
c.2326C>G (p.Arg776Gly)
7g.150948945G=CA1752431955KCNH2n.3336C=
c.2503C= (p.Arg835=)
c.1483C= (p.Arg495=)
c.2203C= (p.Arg735=)
c.2353C= (p.Arg785=)
c.2326C= (p.Arg776=)
7g.150948945G>TCA458645162KCNH2n.3336C>A
c.2503C>A (p.Arg835=)
c.1483C>A (p.Arg495=)
c.2203C>A (p.Arg735=)
c.2353C>A (p.Arg785=)
c.2326C>A (p.Arg776=)
 dbSNP gnomAD v2 gnomAD v4
7g.150948946A>CCA369855035KCNH2n.3335T>G
c.2502T>G (p.His834Gln)
c.1482T>G (p.His494Gln)
c.2202T>G (p.His734Gln)
c.2352T>G (p.His784Gln)
c.2325T>G (p.His775Gln)
7g.150948946A>GCA458645163KCNH2n.3335T>C
c.2502T>C (p.His834=)
c.1482T>C (p.His494=)
c.2202T>C (p.His734=)
c.2352T>C (p.His784=)
c.2325T>C (p.His775=)
7g.150948946A>TCA369855038KCNH2n.3335T>A
c.2502T>A (p.His834Gln)
c.1482T>A (p.His494Gln)
c.2202T>A (p.His734Gln)
c.2352T>A (p.His784Gln)
c.2325T>A (p.His775Gln)
7g.150948947T>ACA369855040KCNH2n.3334A>T
c.2501A>T (p.His834Leu)
c.1481A>T (p.His494Leu)
c.2201A>T (p.His734Leu)
c.2351A>T (p.His784Leu)
c.2324A>T (p.His775Leu)
7g.150948947T>CCA032931KCNH2n.3334A>G
c.2501A>G (p.His834Arg)
c.1481A>G (p.His494Arg)
c.2201A>G (p.His734Arg)
c.2351A>G (p.His784Arg)
c.2324A>G (p.His775Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.150948947T>GCA369855042KCNH2n.3334A>C
c.2501A>C (p.His834Pro)
c.1481A>C (p.His494Pro)
c.2201A>C (p.His734Pro)
c.2351A>C (p.His784Pro)
c.2324A>C (p.His775Pro)
7g.150948947T=CA1752431958KCNH2n.3334A=
c.2501A= (p.His834=)
c.1481A= (p.His494=)
c.2201A= (p.His734=)
c.2351A= (p.His784=)
c.2324A= (p.His775=)
7g.150948948G>ACA369855044KCNH2n.3333C>T
c.2500C>T (p.His834Tyr)
c.1480C>T (p.His494Tyr)
c.2200C>T (p.His734Tyr)
c.2350C>T (p.His784Tyr)
c.2323C>T (p.His775Tyr)
 ClinVar dbSNP
7g.150948948G>CCA369855048KCNH2n.3333C>G
c.2500C>G (p.His834Asp)
c.1480C>G (p.His494Asp)
c.2200C>G (p.His734Asp)
c.2350C>G (p.His784Asp)
c.2323C>G (p.His775Asp)
7g.150948948G=CA1752431960KCNH2n.3333C=
c.2500C= (p.His834=)
c.1480C= (p.His494=)
c.2200C= (p.His734=)
c.2350C= (p.His784=)
c.2323C= (p.His775=)
7g.150948948G>TCA369855046KCNH2n.3333C>A
c.2500C>A (p.His834Asn)
c.1480C>A (p.His494Asn)
c.2200C>A (p.His734Asn)
c.2350C>A (p.His784Asn)
c.2323C>A (p.His775Asn)
7g.150948949G>ACA458645165KCNH2n.3332C>T
c.2499C>T (p.Ile833=)
c.1479C>T (p.Ile493=)
c.2199C>T (p.Ile733=)
c.2349C>T (p.Ile783=)
c.2322C>T (p.Ile774=)
7g.150948949G>CCA369855050KCNH2n.3332C>G
c.2499C>G (p.Ile833Met)
c.1479C>G (p.Ile493Met)
c.2199C>G (p.Ile733Met)
c.2349C>G (p.Ile783Met)
c.2322C>G (p.Ile774Met)
7g.150948949G>TCA458645166KCNH2n.3332C>A
c.2499C>A (p.Ile833=)
c.1479C>A (p.Ile493=)
c.2199C>A (p.Ile733=)
c.2349C>A (p.Ile783=)
c.2322C>A (p.Ile774=)
7g.150948950A>CCA369855051KCNH2n.3331T>G
c.2498T>G (p.Ile833Ser)
c.1478T>G (p.Ile493Ser)
c.2198T>G (p.Ile733Ser)
c.2348T>G (p.Ile783Ser)
c.2321T>G (p.Ile774Ser)
7g.150948950A>GCA369855053KCNH2n.3331T>C
c.2498T>C (p.Ile833Thr)
c.1478T>C (p.Ile493Thr)
c.2198T>C (p.Ile733Thr)
c.2348T>C (p.Ile783Thr)
c.2321T>C (p.Ile774Thr)
7g.150948950A>TCA369855054KCNH2n.3331T>A
c.2498T>A (p.Ile833Asn)
c.1478T>A (p.Ile493Asn)
c.2198T>A (p.Ile733Asn)
c.2348T>A (p.Ile783Asn)
c.2321T>A (p.Ile774Asn)
7g.150948951T>ACA369855055KCNH2n.3330A>T
c.2497A>T (p.Ile833Phe)
c.1477A>T (p.Ile493Phe)
c.2197A>T (p.Ile733Phe)
c.2347A>T (p.Ile783Phe)
c.2320A>T (p.Ile774Phe)
7g.150948951T>CCA369855057KCNH2n.3330A>G
c.2497A>G (p.Ile833Val)
c.1477A>G (p.Ile493Val)
c.2197A>G (p.Ile733Val)
c.2347A>G (p.Ile783Val)
c.2320A>G (p.Ile774Val)
7g.150948951T>GCA369855058KCNH2n.3330A>C
c.2497A>C (p.Ile833Leu)
c.1477A>C (p.Ile493Leu)
c.2197A>C (p.Ile733Leu)
c.2347A>C (p.Ile783Leu)
c.2320A>C (p.Ile774Leu)
7g.150948952C>ACA369855059KCNH2n.3329G>T
c.2496G>T (p.Lys832Asn)
c.1476G>T (p.Lys492Asn)
c.2196G>T (p.Lys732Asn)
c.2346G>T (p.Lys782Asn)
c.2319G>T (p.Lys773Asn)
7g.150948952C>GCA369855060KCNH2n.3329G>C
c.2496G>C (p.Lys832Asn)
c.1476G>C (p.Lys492Asn)
c.2196G>C (p.Lys732Asn)
c.2346G>C (p.Lys782Asn)
c.2319G>C (p.Lys773Asn)
7g.150948952C>TCA458645167KCNH2n.3329G>A
c.2496G>A (p.Lys832=)
c.1476G>A (p.Lys492=)
c.2196G>A (p.Lys732=)
c.2346G>A (p.Lys782=)
c.2319G>A (p.Lys773=)
7g.150948953T>ACA369855066KCNH2n.3328A>T
c.2495A>T (p.Lys832Met)
c.1475A>T (p.Lys492Met)
c.2195A>T (p.Lys732Met)
c.2345A>T (p.Lys782Met)
c.2318A>T (p.Lys773Met)
7g.150948953T>CCA369855064KCNH2n.3328A>G
c.2495A>G (p.Lys832Arg)
c.1475A>G (p.Lys492Arg)
c.2195A>G (p.Lys732Arg)
c.2345A>G (p.Lys782Arg)
c.2318A>G (p.Lys773Arg)
7g.150948953T>GCA369855062KCNH2n.3328A>C
c.2495A>C (p.Lys832Thr)
c.1475A>C (p.Lys492Thr)
c.2195A>C (p.Lys732Thr)
c.2345A>C (p.Lys782Thr)
c.2318A>C (p.Lys773Thr)
7g.150948954T>ACA006840KCNH2n.3327A>T
c.2494A>T (p.Lys832Ter)
c.1474A>T (p.Lys492Ter)
c.2194A>T (p.Lys732Ter)
c.2344A>T (p.Lys782Ter)
c.2317A>T (p.Lys773Ter)
 ClinVar dbSNP gnomAD v4
7g.150948954T>CCA369855068KCNH2n.3327A>G
c.2494A>G (p.Lys832Glu)
c.1474A>G (p.Lys492Glu)
c.2194A>G (p.Lys732Glu)
c.2344A>G (p.Lys782Glu)
c.2317A>G (p.Lys773Glu)
7g.150948954T>GCA369855070KCNH2n.3327A>C
c.2494A>C (p.Lys832Gln)
c.1474A>C (p.Lys492Gln)
c.2194A>C (p.Lys732Gln)
c.2344A>C (p.Lys782Gln)
c.2317A>C (p.Lys773Gln)
7g.150948954T=CA1752431961KCNH2n.3327A=
c.2494A= (p.Lys832=)
c.1474A= (p.Lys492=)
c.2194A= (p.Lys732=)
c.2344A= (p.Lys782=)
c.2317A= (p.Lys773=)
7g.150948955G>ACA458645168KCNH2n.3326C>T
c.2493C>T (p.His831=)
c.1473C>T (p.His491=)
c.2193C>T (p.His731=)
c.2343C>T (p.His781=)
c.2316C>T (p.His772=)
 gnomAD v4
7g.150948955G>CCA369855071KCNH2n.3326C>G
c.2493C>G (p.His831Gln)
c.1473C>G (p.His491Gln)
c.2193C>G (p.His731Gln)
c.2343C>G (p.His781Gln)
c.2316C>G (p.His772Gln)
7g.150948955G>TCA369855073KCNH2n.3326C>A
c.2493C>A (p.His831Gln)
c.1473C>A (p.His491Gln)
c.2193C>A (p.His731Gln)
c.2343C>A (p.His781Gln)
c.2316C>A (p.His772Gln)
7g.150948956T>ACA369855078KCNH2n.3325A>T
c.2492A>T (p.His831Leu)
c.1472A>T (p.His491Leu)
c.2192A>T (p.His731Leu)
c.2342A>T (p.His781Leu)
c.2315A>T (p.His772Leu)
7g.150948956T>CCA369855077KCNH2n.3325A>G
c.2492A>G (p.His831Arg)
c.1472A>G (p.His491Arg)
c.2192A>G (p.His731Arg)
c.2342A>G (p.His781Arg)
c.2315A>G (p.His772Arg)
 gnomAD v4
7g.150948956T>GCA369855075KCNH2n.3325A>C
c.2492A>C (p.His831Pro)
c.1472A>C (p.His491Pro)
c.2192A>C (p.His731Pro)
c.2342A>C (p.His781Pro)
c.2315A>C (p.His772Pro)
7g.150948956_150948966delinsTGTAGGTCACACA1752431965KCNH2n.3315_3325delinsTGTGACCTACA
c.2482_2492delinsTGTGACCTACA (p.Cys828=)
c.1462_1472delinsTGTGACCTACA (p.Cys488=)
c.2182_2192delinsTGTGACCTACA (p.Cys728=)
c.2332_2342delinsTGTGACCTACA (p.Cys778=)
c.2305_2315delinsTGTGACCTACA (p.Cys769=)
7g.150948957G>ACA369855081KCNH2n.3324C>T
c.2491C>T (p.His831Tyr)
c.1471C>T (p.His491Tyr)
c.2191C>T (p.His731Tyr)
c.2341C>T (p.His781Tyr)
c.2314C>T (p.His772Tyr)
 ClinVar
7g.150948957G>CCA369855083KCNH2n.3324C>G
c.2491C>G (p.His831Asp)
c.1471C>G (p.His491Asp)
c.2191C>G (p.His731Asp)
c.2341C>G (p.His781Asp)
c.2314C>G (p.His772Asp)
7g.150948957G>TCA369855084KCNH2n.3324C>A
c.2491C>A (p.His831Asn)
c.1471C>A (p.His491Asn)
c.2191C>A (p.His731Asn)
c.2341C>A (p.His781Asn)
c.2314C>A (p.His772Asn)
7g.150948963_150948972delCA658797039KCNH2n.3315_3324del
c.2482_2491del (p.Cys828ThrfsTer?)
c.1462_1471del (p.Cys488ThrfsTer?)
c.2182_2191del (p.Cys728ThrfsTer?)
c.2332_2341del (p.Cys778ThrfsTer?)
c.2305_2314del (p.Cys769ThrfsTer?)
 ClinVar dbSNP gnomAD v4
7g.150948958T>ACA458645169KCNH2n.3323A>T
c.2490A>T (p.Leu830=)
c.1470A>T (p.Leu490=)
c.2190A>T (p.Leu730=)
c.2340A>T (p.Leu780=)
c.2313A>T (p.Leu771=)
7g.150948958T>CCA458645170KCNH2n.3323A>G
c.2490A>G (p.Leu830=)
c.1470A>G (p.Leu490=)
c.2190A>G (p.Leu730=)
c.2340A>G (p.Leu780=)
c.2313A>G (p.Leu771=)
7g.150948958T>GCA458645171KCNH2n.3323A>C
c.2490A>C (p.Leu830=)
c.1470A>C (p.Leu490=)
c.2190A>C (p.Leu730=)
c.2340A>C (p.Leu780=)
c.2313A>C (p.Leu771=)
7g.150948959A>CCA369855087KCNH2n.3322T>G
c.2489T>G (p.Leu830Arg)
c.1469T>G (p.Leu490Arg)
c.2189T>G (p.Leu730Arg)
c.2339T>G (p.Leu780Arg)
c.2312T>G (p.Leu771Arg)
7g.150948959A>GCA369855088KCNH2n.3322T>C
c.2489T>C (p.Leu830Pro)
c.1469T>C (p.Leu490Pro)
c.2189T>C (p.Leu730Pro)
c.2339T>C (p.Leu780Pro)
c.2312T>C (p.Leu771Pro)
7g.150948959A>TCA369855090KCNH2n.3322T>A
c.2489T>A (p.Leu830Gln)
c.1469T>A (p.Leu490Gln)
c.2189T>A (p.Leu730Gln)
c.2339T>A (p.Leu780Gln)
c.2312T>A (p.Leu771Gln)
7g.150948960G>ACA032910KCNH2n.3321C>T
c.2488C>T (p.Leu830=)
c.1468C>T (p.Leu490=)
c.2188C>T (p.Leu730=)
c.2338C>T (p.Leu780=)
c.2311C>T (p.Leu771=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.150948960G>CCA369855093KCNH2n.3321C>G
c.2488C>G (p.Leu830Val)
c.1468C>G (p.Leu490Val)
c.2188C>G (p.Leu730Val)
c.2338C>G (p.Leu780Val)
c.2311C>G (p.Leu771Val)
 ClinVar gnomAD v4
7g.150948960G=CA1752431969KCNH2n.3321C=
c.2488C= (p.Leu830=)
c.1468C= (p.Leu490=)
c.2188C= (p.Leu730=)
c.2338C= (p.Leu780=)
c.2311C= (p.Leu771=)
7g.150948960G>TCA369855092KCNH2n.3321C>A
c.2488C>A (p.Leu830Ile)
c.1468C>A (p.Leu490Ile)
c.2188C>A (p.Leu730Ile)
c.2338C>A (p.Leu780Ile)
c.2311C>A (p.Leu771Ile)
7g.150948964_150949161delCA2573141856KCNH2n.3232-108_3321del
c.2399-108_2488del
c.1379-108_1468del
c.2099-108_2188del
c.2249-108_2338del
c.2222-108_2311del
 ClinVar dbSNP
7g.150948961G>ACA458645172KCNH2n.3320C>T
c.2487C>T (p.Asp829=)
c.1467C>T (p.Asp489=)
c.2187C>T (p.Asp729=)
c.2337C>T (p.Asp779=)
c.2310C>T (p.Asp770=)
7g.150948961G>CCA032903KCNH2n.3320C>G
c.2487C>G (p.Asp829Glu)
c.1467C>G (p.Asp489Glu)
c.2187C>G (p.Asp729Glu)
c.2337C>G (p.Asp779Glu)
c.2310C>G (p.Asp770Glu)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.150948961G=CA1752431970KCNH2n.3320C=
c.2487C= (p.Asp829=)
c.1467C= (p.Asp489=)
c.2187C= (p.Asp729=)
c.2337C= (p.Asp779=)
c.2310C= (p.Asp770=)
7g.150948961G>TCA369855096KCNH2n.3320C>A
c.2487C>A (p.Asp829Glu)
c.1467C>A (p.Asp489Glu)
c.2187C>A (p.Asp729Glu)
c.2337C>A (p.Asp779Glu)
c.2310C>A (p.Asp770Glu)
7g.150948962T>ACA369855098KCNH2n.3319A>T
c.2486A>T (p.Asp829Val)
c.1466A>T (p.Asp489Val)
c.2186A>T (p.Asp729Val)
c.2336A>T (p.Asp779Val)
c.2309A>T (p.Asp770Val)
7g.150948962T>CCA369855100KCNH2n.3319A>G
c.2486A>G (p.Asp829Gly)
c.1466A>G (p.Asp489Gly)
c.2186A>G (p.Asp729Gly)
c.2336A>G (p.Asp779Gly)
c.2309A>G (p.Asp770Gly)
 COSMIC COSMIC
7g.150948962T>GCA369855102KCNH2n.3319A>C
c.2486A>C (p.Asp829Ala)
c.1466A>C (p.Asp489Ala)
c.2186A>C (p.Asp729Ala)
c.2336A>C (p.Asp779Ala)
c.2309A>C (p.Asp770Ala)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150948962T=CA1752431973KCNH2n.3319A=
c.2486A= (p.Asp829=)
c.1466A= (p.Asp489=)
c.2186A= (p.Asp729=)
c.2336A= (p.Asp779=)
c.2309A= (p.Asp770=)
7g.150948963C>ACA369855104KCNH2n.3318G>T
c.2485G>T (p.Asp829Tyr)
c.1465G>T (p.Asp489Tyr)
c.2185G>T (p.Asp729Tyr)
c.2335G>T (p.Asp779Tyr)
c.2308G>T (p.Asp770Tyr)
7g.150948963C>GCA369855106KCNH2n.3318G>C
c.2485G>C (p.Asp829His)
c.1465G>C (p.Asp489His)
c.2185G>C (p.Asp729His)
c.2335G>C (p.Asp779His)
c.2308G>C (p.Asp770His)
7g.150948963C>TCA369855108KCNH2n.3318G>A
c.2485G>A (p.Asp829Asn)
c.1465G>A (p.Asp489Asn)
c.2185G>A (p.Asp729Asn)
c.2335G>A (p.Asp779Asn)
c.2308G>A (p.Asp770Asn)
7g.150948964A>CCA369855110KCNH2n.3317T>G
c.2484T>G (p.Cys828Trp)
c.1464T>G (p.Cys488Trp)
c.2184T>G (p.Cys728Trp)
c.2334T>G (p.Cys778Trp)
c.2307T>G (p.Cys769Trp)
7g.150948964A>GCA458645173KCNH2n.3317T>C
c.2484T>C (p.Cys828=)
c.1464T>C (p.Cys488=)
c.2184T>C (p.Cys728=)
c.2334T>C (p.Cys778=)
c.2307T>C (p.Cys769=)
7g.150948964A>TCA369855112KCNH2n.3317T>A
c.2484T>A (p.Cys828Ter)
c.1464T>A (p.Cys488Ter)
c.2184T>A (p.Cys728Ter)
c.2334T>A (p.Cys778Ter)
c.2307T>A (p.Cys769Ter)
7g.150948964_150948967delCA2530854113KCNH2n.3314_3317del
c.2481_2484del (p.Tyr827Ter)
c.1461_1464del (p.Tyr487Ter)
c.2181_2184del (p.Tyr727Ter)
c.2331_2334del (p.Tyr777Ter)
c.2304_2307del (p.Tyr768Ter)
7g.150948965C>ACA369855117KCNH2n.3316G>T
c.2483G>T (p.Cys828Phe)
c.1463G>T (p.Cys488Phe)
c.2183G>T (p.Cys728Phe)
c.2333G>T (p.Cys778Phe)
c.2306G>T (p.Cys769Phe)
7g.150948965C>GCA369855116KCNH2n.3316G>C
c.2483G>C (p.Cys828Ser)
c.1463G>C (p.Cys488Ser)
c.2183G>C (p.Cys728Ser)
c.2333G>C (p.Cys778Ser)
c.2306G>C (p.Cys769Ser)
7g.150948965C>TCA369855114KCNH2n.3316G>A
c.2483G>A (p.Cys828Tyr)
c.1463G>A (p.Cys488Tyr)
c.2183G>A (p.Cys728Tyr)
c.2333G>A (p.Cys778Tyr)
c.2306G>A (p.Cys769Tyr)
7g.150948966A=CA1752431979KCNH2n.3315T=
c.2482T= (p.Cys828=)
c.1462T= (p.Cys488=)
c.2182T= (p.Cys728=)
c.2332T= (p.Cys778=)
c.2305T= (p.Cys769=)
7g.150948966A>CCA369855120KCNH2n.3315T>G
c.2482T>G (p.Cys828Gly)
c.1462T>G (p.Cys488Gly)
c.2182T>G (p.Cys728Gly)
c.2332T>G (p.Cys778Gly)
c.2305T>G (p.Cys769Gly)
7g.150948966A>GCA369855122KCNH2n.3315T>C
c.2482T>C (p.Cys828Arg)
c.1462T>C (p.Cys488Arg)
c.2182T>C (p.Cys728Arg)
c.2332T>C (p.Cys778Arg)
c.2305T>C (p.Cys769Arg)
 ClinVar dbSNP gnomAD v4
7g.150948966A>TCA369855121KCNH2n.3315T>A
c.2482T>A (p.Cys828Ser)
c.1462T>A (p.Cys488Ser)
c.2182T>A (p.Cys728Ser)
c.2332T>A (p.Cys778Ser)
c.2305T>A (p.Cys769Ser)
 ClinVar gnomAD v4
7g.150948967G>ACA458645174KCNH2n.3314C>T
c.2481C>T (p.Tyr827=)
c.1461C>T (p.Tyr487=)
c.2181C>T (p.Tyr727=)
c.2331C>T (p.Tyr777=)
c.2304C>T (p.Tyr768=)
7g.150948967G>CCA369855124KCNH2n.3314C>G
c.2481C>G (p.Tyr827Ter)
c.1461C>G (p.Tyr487Ter)
c.2181C>G (p.Tyr727Ter)
c.2331C>G (p.Tyr777Ter)
c.2304C>G (p.Tyr768Ter)
7g.150948967G>TCA369855126KCNH2n.3314C>A
c.2481C>A (p.Tyr827Ter)
c.1461C>A (p.Tyr487Ter)
c.2181C>A (p.Tyr727Ter)
c.2331C>A (p.Tyr777Ter)
c.2304C>A (p.Tyr768Ter)
7g.150948968T>ACA369855128KCNH2n.3313A>T
c.2480A>T (p.Tyr827Phe)
c.1460A>T (p.Tyr487Phe)
c.2180A>T (p.Tyr727Phe)
c.2330A>T (p.Tyr777Phe)
c.2303A>T (p.Tyr768Phe)
7g.150948968T>CCA369855130KCNH2n.3313A>G
c.2480A>G (p.Tyr827Cys)
c.1460A>G (p.Tyr487Cys)
c.2180A>G (p.Tyr727Cys)
c.2330A>G (p.Tyr777Cys)
c.2303A>G (p.Tyr768Cys)
7g.150948968T>GCA369855132KCNH2n.3313A>C
c.2480A>C (p.Tyr827Ser)
c.1460A>C (p.Tyr487Ser)
c.2180A>C (p.Tyr727Ser)
c.2330A>C (p.Tyr777Ser)
c.2303A>C (p.Tyr768Ser)
7g.150948969A>CCA369855134KCNH2n.3312T>G
c.2479T>G (p.Tyr827Asp)
c.1459T>G (p.Tyr487Asp)
c.2179T>G (p.Tyr727Asp)
c.2329T>G (p.Tyr777Asp)
c.2302T>G (p.Tyr768Asp)
7g.150948969A>GCA369855136KCNH2n.3312T>C
c.2479T>C (p.Tyr827His)
c.1459T>C (p.Tyr487His)
c.2179T>C (p.Tyr727His)
c.2329T>C (p.Tyr777His)
c.2302T>C (p.Tyr768His)
7g.150948969A>TCA369855137KCNH2n.3312T>A
c.2479T>A (p.Tyr827Asn)
c.1459T>A (p.Tyr487Asn)
c.2179T>A (p.Tyr727Asn)
c.2329T>A (p.Tyr777Asn)
c.2302T>A (p.Tyr768Asn)
7g.150948970G>ACA032883KCNH2n.3311C>T
c.2478C>T (p.Thr826=)
c.1458C>T (p.Thr486=)
c.2178C>T (p.Thr726=)
c.2328C>T (p.Thr776=)
c.2301C>T (p.Thr767=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.150948970G>CCA458645175KCNH2n.3311C>G
c.2478C>G (p.Thr826=)
c.1458C>G (p.Thr486=)
c.2178C>G (p.Thr726=)
c.2328C>G (p.Thr776=)
c.2301C>G (p.Thr767=)
7g.150948970G=CA1752431985KCNH2n.3311C=
c.2478C= (p.Thr826=)
c.1458C= (p.Thr486=)
c.2178C= (p.Thr726=)
c.2328C= (p.Thr776=)
c.2301C= (p.Thr767=)
7g.150948970G>TCA458645176KCNH2n.3311C>A
c.2478C>A (p.Thr826=)
c.1458C>A (p.Thr486=)
c.2178C>A (p.Thr726=)
c.2328C>A (p.Thr776=)
c.2301C>A (p.Thr767=)
7g.150948971G>ACA006823KCNH2n.3310C>T
c.2477C>T (p.Thr826Ile)
c.1457C>T (p.Thr486Ile)
c.2177C>T (p.Thr726Ile)
c.2327C>T (p.Thr776Ile)
c.2300C>T (p.Thr767Ile)
 ClinVar dbSNP gnomAD v4
7g.150948971G>CCA369855140KCNH2n.3310C>G
c.2477C>G (p.Thr826Ser)
c.1457C>G (p.Thr486Ser)
c.2177C>G (p.Thr726Ser)
c.2327C>G (p.Thr776Ser)
c.2300C>G (p.Thr767Ser)
 dbSNP
7g.150948971G=CA1752431987KCNH2n.3310C=
c.2477C= (p.Thr826=)
c.1457C= (p.Thr486=)
c.2177C= (p.Thr726=)
c.2327C= (p.Thr776=)
c.2300C= (p.Thr767=)
7g.150948971G>TCA369855142KCNH2n.3310C>A
c.2477C>A (p.Thr826Asn)
c.1457C>A (p.Thr486Asn)
c.2177C>A (p.Thr726Asn)
c.2327C>A (p.Thr776Asn)
c.2300C>A (p.Thr767Asn)
7g.150948972T>ACA369855145KCNH2n.3309A>T
c.2476A>T (p.Thr826Ser)
c.1456A>T (p.Thr486Ser)
c.2176A>T (p.Thr726Ser)
c.2326A>T (p.Thr776Ser)
c.2299A>T (p.Thr767Ser)
7g.150948972T>CCA369855147KCNH2n.3309A>G
c.2476A>G (p.Thr826Ala)
c.1456A>G (p.Thr486Ala)
c.2176A>G (p.Thr726Ala)
c.2326A>G (p.Thr776Ala)
c.2299A>G (p.Thr767Ala)
 gnomAD v4
7g.150948972T>GCA369855146KCNH2n.3309A>C
c.2476A>C (p.Thr826Pro)
c.1456A>C (p.Thr486Pro)
c.2176A>C (p.Thr726Pro)
c.2326A>C (p.Thr776Pro)
c.2299A>C (p.Thr767Pro)
7g.150948973G>ACA169074818KCNH2n.3308C>T
c.2475C>T (p.Leu825=)
c.1455C>T (p.Leu485=)
c.2175C>T (p.Leu725=)
c.2325C>T (p.Leu775=)
c.2298C>T (p.Leu766=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150948973G>CCA458645177KCNH2n.3308C>G
c.2475C>G (p.Leu825=)
c.1455C>G (p.Leu485=)
c.2175C>G (p.Leu725=)
c.2325C>G (p.Leu775=)
c.2298C>G (p.Leu766=)
7g.150948973G=CA1752431992KCNH2n.3308C=
c.2475C= (p.Leu825=)
c.1455C= (p.Leu485=)
c.2175C= (p.Leu725=)
c.2325C= (p.Leu775=)
c.2298C= (p.Leu766=)
7g.150948973G>TCA458645178KCNH2n.3308C>A
c.2475C>A (p.Leu825=)
c.1455C>A (p.Leu485=)
c.2175C>A (p.Leu725=)
c.2325C>A (p.Leu775=)
c.2298C>A (p.Leu766=)
7g.150948974_150948975delCA2507623695KCNH2n.3307_3308del
c.2474_2475del (p.Leu825HisfsTer4)
c.1454_1455del (p.Leu485HisfsTer4)
c.2174_2175del (p.Leu725HisfsTer4)
c.2324_2325del (p.Leu775HisfsTer4)
c.2297_2298del (p.Leu766HisfsTer4)
7g.150948974A>CCA369855151KCNH2n.3307T>G
c.2474T>G (p.Leu825Arg)
c.1454T>G (p.Leu485Arg)
c.2174T>G (p.Leu725Arg)
c.2324T>G (p.Leu775Arg)
c.2297T>G (p.Leu766Arg)
7g.150948974A>GCA369855153KCNH2n.3307T>C
c.2474T>C (p.Leu825Pro)
c.1454T>C (p.Leu485Pro)
c.2174T>C (p.Leu725Pro)
c.2324T>C (p.Leu775Pro)
c.2297T>C (p.Leu766Pro)
7g.150948974A>TCA369855154KCNH2n.3307T>A
c.2474T>A (p.Leu825His)
c.1454T>A (p.Leu485His)
c.2174T>A (p.Leu725His)
c.2324T>A (p.Leu775His)
c.2297T>A (p.Leu766His)
7g.150948975_150948983dupCA1139660303KCNH2n.3299_3307dup
c.2466_2474dup (p.Leu825_Thr826insArgAlaLeu)
c.1446_1454dup (p.Leu485_Thr486insArgAlaLeu)
c.2166_2174dup (p.Leu725_Thr726insArgAlaLeu)
c.2316_2324dup (p.Leu775_Thr776insArgAlaLeu)
c.2289_2297dup (p.Leu766_Thr767insArgAlaLeu)
 ClinVar dbSNP
7g.150948975G>ACA369855156KCNH2n.3306C>T
c.2473C>T (p.Leu825Phe)
c.1453C>T (p.Leu485Phe)
c.2173C>T (p.Leu725Phe)
c.2323C>T (p.Leu775Phe)
c.2296C>T (p.Leu766Phe)
7g.150948975G>CCA369855157KCNH2n.3306C>G
c.2473C>G (p.Leu825Val)
c.1453C>G (p.Leu485Val)
c.2173C>G (p.Leu725Val)
c.2323C>G (p.Leu775Val)
c.2296C>G (p.Leu766Val)
7g.150948975G>TCA369855158KCNH2n.3306C>A
c.2473C>A (p.Leu825Ile)
c.1453C>A (p.Leu485Ile)
c.2173C>A (p.Leu725Ile)
c.2323C>A (p.Leu775Ile)
c.2296C>A (p.Leu766Ile)
7g.150948976G>ACA458645179KCNH2n.3305C>T
c.2472C>T (p.Ala824=)
c.1452C>T (p.Ala484=)
c.2172C>T (p.Ala724=)
c.2322C>T (p.Ala774=)
c.2295C>T (p.Ala765=)
 ClinVar
7g.150948976G>CCA458645180KCNH2n.3305C>G
c.2472C>G (p.Ala824=)
c.1452C>G (p.Ala484=)
c.2172C>G (p.Ala724=)
c.2322C>G (p.Ala774=)
c.2295C>G (p.Ala765=)
 gnomAD v4
7g.150948976G>TCA458645181KCNH2n.3305C>A
c.2472C>A (p.Ala824=)
c.1452C>A (p.Ala484=)
c.2172C>A (p.Ala724=)
c.2322C>A (p.Ala774=)
c.2295C>A (p.Ala765=)
7g.150948977G>ACA369855159KCNH2n.3304C>T
c.2471C>T (p.Ala824Val)
c.1451C>T (p.Ala484Val)
c.2171C>T (p.Ala724Val)
c.2321C>T (p.Ala774Val)
c.2294C>T (p.Ala765Val)
7g.150948977G>CCA369855160KCNH2n.3304C>G
c.2471C>G (p.Ala824Gly)
c.1451C>G (p.Ala484Gly)
c.2171C>G (p.Ala724Gly)
c.2321C>G (p.Ala774Gly)
c.2294C>G (p.Ala765Gly)
7g.150948977G>TCA369855162KCNH2n.3304C>A
c.2471C>A (p.Ala824Asp)
c.1451C>A (p.Ala484Asp)
c.2171C>A (p.Ala724Asp)
c.2321C>A (p.Ala774Asp)
c.2294C>A (p.Ala765Asp)
7g.150948977_150948978delinsGCCA1752431999KCNH2n.3303_3304delinsGC
c.2470_2471delinsGC (p.Ala824=)
c.1450_1451delinsGC (p.Ala484=)
c.2170_2171delinsGC (p.Ala724=)
c.2320_2321delinsGC (p.Ala774=)
c.2293_2294delinsGC (p.Ala765=)
7g.150948978C>ACA369855166KCNH2n.3303G>T
c.2470G>T (p.Ala824Ser)
c.1450G>T (p.Ala484Ser)
c.2170G>T (p.Ala724Ser)
c.2320G>T (p.Ala774Ser)
c.2293G>T (p.Ala765Ser)
7g.150948978C>GCA369855168KCNH2n.3303G>C
c.2470G>C (p.Ala824Pro)
c.1450G>C (p.Ala484Pro)
c.2170G>C (p.Ala724Pro)
c.2320G>C (p.Ala774Pro)
c.2293G>C (p.Ala765Pro)
7g.150948978C>TCA369855164KCNH2n.3303G>A
c.2470G>A (p.Ala824Thr)
c.1450G>A (p.Ala484Thr)
c.2170G>A (p.Ala724Thr)
c.2320G>A (p.Ala774Thr)
c.2293G>A (p.Ala765Thr)
7g.150948980dupCA2695208827KCNH2n.3303dup
c.2470dup (p.Ala824GlyfsTer6)
c.1450dup (p.Ala484GlyfsTer6)
c.2170dup (p.Ala724GlyfsTer6)
c.2320dup (p.Ala774GlyfsTer6)
c.2293dup (p.Ala765GlyfsTer6)
7g.150948980delCA16618402KCNH2n.3303del
c.2470del (p.Ala824ProfsTer?)
c.1450del (p.Ala484ProfsTer?)
c.2170del (p.Ala724ProfsTer?)
c.2320del (p.Ala774ProfsTer?)
c.2293del (p.Ala765ProfsTer?)
 ClinVar dbSNP
7g.150948978_150948979insGCA2514231751KCNH2n.3302_3303insC
c.2469_2470insC (p.Ala824ArgfsTer6)
c.1449_1450insC (p.Ala484ArgfsTer6)
c.2169_2170insC (p.Ala724ArgfsTer6)
c.2319_2320insC (p.Ala774ArgfsTer6)
c.2292_2293insC (p.Ala765ArgfsTer6)
7g.150948979C>ACA458645182KCNH2n.3302G>T
c.2469G>T (p.Arg823=)
c.1449G>T (p.Arg483=)
c.2169G>T (p.Arg723=)
c.2319G>T (p.Arg773=)
c.2292G>T (p.Arg764=)
7g.150948979C>GCA458645183KCNH2n.3302G>C
c.2469G>C (p.Arg823=)
c.1449G>C (p.Arg483=)
c.2169G>C (p.Arg723=)
c.2319G>C (p.Arg773=)
c.2292G>C (p.Arg764=)
7g.150948979C>TCA458645184KCNH2n.3302G>A
c.2469G>A (p.Arg823=)
c.1449G>A (p.Arg483=)
c.2169G>A (p.Arg723=)
c.2319G>A (p.Arg773=)
c.2292G>A (p.Arg764=)
 COSMIC COSMIC
7g.150948980C>ACA369855170KCNH2n.3301G>T
c.2468G>T (p.Arg823Leu)
c.1448G>T (p.Arg483Leu)
c.2168G>T (p.Arg723Leu)
c.2318G>T (p.Arg773Leu)
c.2291G>T (p.Arg764Leu)
 ClinVar gnomAD v4
7g.150948980C=CA1752432004KCNH2n.3301G=
c.2468G= (p.Arg823=)
c.1448G= (p.Arg483=)
c.2168G= (p.Arg723=)
c.2318G= (p.Arg773=)
c.2291G= (p.Arg764=)
7g.150948980C>GCA369855171KCNH2n.3301G>C
c.2468G>C (p.Arg823Pro)
c.1448G>C (p.Arg483Pro)
c.2168G>C (p.Arg723Pro)
c.2318G>C (p.Arg773Pro)
c.2291G>C (p.Arg764Pro)
 ClinVar dbSNP
7g.150948980C>TCA16618403KCNH2n.3301G>A
c.2468G>A (p.Arg823Gln)
c.1448G>A (p.Arg483Gln)
c.2168G>A (p.Arg723Gln)
c.2318G>A (p.Arg773Gln)
c.2291G>A (p.Arg764Gln)
 ClinVar dbSNP gnomAD v4
7g.150948981G>ACA006812KCNH2n.3300C>T
c.2467C>T (p.Arg823Trp)
c.1447C>T (p.Arg483Trp)
c.2167C>T (p.Arg723Trp)
c.2317C>T (p.Arg773Trp)
c.2290C>T (p.Arg764Trp)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150948981G>CCA369855174KCNH2n.3300C>G
c.2467C>G (p.Arg823Gly)
c.1447C>G (p.Arg483Gly)
c.2167C>G (p.Arg723Gly)
c.2317C>G (p.Arg773Gly)
c.2290C>G (p.Arg764Gly)
7g.150948981G=CA1752432008KCNH2n.3300C=
c.2467C= (p.Arg823=)
c.1447C= (p.Arg483=)
c.2167C= (p.Arg723=)
c.2317C= (p.Arg773=)
c.2290C= (p.Arg764=)
7g.150948981G>TCA458645185KCNH2n.3300C>A
c.2467C>A (p.Arg823=)
c.1447C>A (p.Arg483=)
c.2167C>A (p.Arg723=)
c.2317C>A (p.Arg773=)
c.2290C>A (p.Arg764=)
7g.150948982C>ACA458645186KCNH2n.3299G>T
c.2466G>T (p.Val822=)
c.1446G>T (p.Val482=)
c.2166G>T (p.Val722=)
c.2316G>T (p.Val772=)
c.2289G>T (p.Val763=)
7g.150948982C=CA1752432013KCNH2n.3299G=
c.2466G= (p.Val822=)
c.1446G= (p.Val482=)
c.2166G= (p.Val722=)
c.2316G= (p.Val772=)
c.2289G= (p.Val763=)
7g.150948982C>GCA032868KCNH2n.3299G>C
c.2466G>C (p.Val822=)
c.1446G>C (p.Val482=)
c.2166G>C (p.Val722=)
c.2316G>C (p.Val772=)
c.2289G>C (p.Val763=)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.150948982C>TCA458645187KCNH2n.3299G>A
c.2466G>A (p.Val822=)
c.1446G>A (p.Val482=)
c.2166G>A (p.Val722=)
c.2316G>A (p.Val772=)
c.2289G>A (p.Val763=)
7g.150948983A>CCA369855181KCNH2n.3298T>G
c.2465T>G (p.Val822Gly)
c.1445T>G (p.Val482Gly)
c.2165T>G (p.Val722Gly)
c.2315T>G (p.Val772Gly)
c.2288T>G (p.Val763Gly)
7g.150948983A>GCA369855178KCNH2n.3298T>C
c.2465T>C (p.Val822Ala)
c.1445T>C (p.Val482Ala)
c.2165T>C (p.Val722Ala)
c.2315T>C (p.Val772Ala)
c.2288T>C (p.Val763Ala)
 ClinVar
7g.150948983A>TCA369855179KCNH2n.3298T>A
c.2465T>A (p.Val822Glu)
c.1445T>A (p.Val482Glu)
c.2165T>A (p.Val722Glu)
c.2315T>A (p.Val772Glu)
c.2288T>A (p.Val763Glu)
7g.150948983_150948986delinsCCCTCCA2695208828KCNH2n.3295_3298delinsGAGGG
c.2462_2465delinsGAGGG (p.Asp821GlyfsTer9)
c.1442_1445delinsGAGGG (p.Asp481GlyfsTer9)
c.2162_2165delinsGAGGG (p.Asp721GlyfsTer9)
c.2312_2315delinsGAGGG (p.Asp771GlyfsTer9)
c.2285_2288delinsGAGGG (p.Asp762GlyfsTer9)
7g.150948983_150948984insTCA2502903432KCNH2n.3297_3298insA
c.2464_2465insA (p.Val822AspfsTer8)
c.1444_1445insA (p.Val482AspfsTer8)
c.2164_2165insA (p.Val722AspfsTer8)
c.2314_2315insA (p.Val772AspfsTer8)
c.2287_2288insA (p.Val763AspfsTer8)
7g.150948984C>ACA369855183KCNH2n.3297G>T
c.2464G>T (p.Val822Leu)
c.1444G>T (p.Val482Leu)
c.2164G>T (p.Val722Leu)
c.2314G>T (p.Val772Leu)
c.2287G>T (p.Val763Leu)
7g.150948984C=CA1752432020KCNH2n.3297G=
c.2464G= (p.Val822=)
c.1444G= (p.Val482=)
c.2164G= (p.Val722=)
c.2314G= (p.Val772=)
c.2287G= (p.Val763=)
7g.150948984C>GCA006804KCNH2n.3297G>C
c.2464G>C (p.Val822Leu)
c.1444G>C (p.Val482Leu)
c.2164G>C (p.Val722Leu)
c.2314G>C (p.Val772Leu)
c.2287G>C (p.Val763Leu)
 ClinVar dbSNP
7g.150948984C>TCA006796KCNH2n.3297G>A
c.2464G>A (p.Val822Met)
c.1444G>A (p.Val482Met)
c.2164G>A (p.Val722Met)
c.2314G>A (p.Val772Met)
c.2287G>A (p.Val763Met)
 ClinVar dbSNP
7g.150948985A=CA1752432021KCNH2n.3296T=
c.2463T= (p.Asp821=)
c.1443T= (p.Asp481=)
c.2163T= (p.Asp721=)
c.2313T= (p.Asp771=)
c.2286T= (p.Asp762=)
7g.150948985A>CCA369855187KCNH2n.3296T>G
c.2463T>G (p.Asp821Glu)
c.1443T>G (p.Asp481Glu)
c.2163T>G (p.Asp721Glu)
c.2313T>G (p.Asp771Glu)
c.2286T>G (p.Asp762Glu)
7g.150948985A>GCA458645188KCNH2n.3296T>C
c.2463T>C (p.Asp821=)
c.1443T>C (p.Asp481=)
c.2163T>C (p.Asp721=)
c.2313T>C (p.Asp771=)
c.2286T>C (p.Asp762=)
 ClinVar dbSNP gnomAD v4
7g.150948985A>TCA369855189KCNH2n.3296T>A
c.2463T>A (p.Asp821Glu)
c.1443T>A (p.Asp481Glu)
c.2163T>A (p.Asp721Glu)
c.2313T>A (p.Asp771Glu)
c.2286T>A (p.Asp762Glu)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150948986T>ACA369855191KCNH2n.3295A>T
c.2462A>T (p.Asp821Val)
c.1442A>T (p.Asp481Val)
c.2162A>T (p.Asp721Val)
c.2312A>T (p.Asp771Val)
c.2285A>T (p.Asp762Val)
 ClinVar dbSNP
7g.150948986T>CCA369855193KCNH2n.3295A>G
c.2462A>G (p.Asp821Gly)
c.1442A>G (p.Asp481Gly)
c.2162A>G (p.Asp721Gly)
c.2312A>G (p.Asp771Gly)
c.2285A>G (p.Asp762Gly)
7g.150948986T>GCA369855192KCNH2n.3295A>C
c.2462A>C (p.Asp821Ala)
c.1442A>C (p.Asp481Ala)
c.2162A>C (p.Asp721Ala)
c.2312A>C (p.Asp771Ala)
c.2285A>C (p.Asp762Ala)
7g.150948987C>ACA369855196KCNH2n.3294G>T
c.2461G>T (p.Asp821Tyr)
c.1441G>T (p.Asp481Tyr)
c.2161G>T (p.Asp721Tyr)
c.2311G>T (p.Asp771Tyr)
c.2284G>T (p.Asp762Tyr)
7g.150948987C>GCA369855198KCNH2n.3294G>C
c.2461G>C (p.Asp821His)
c.1441G>C (p.Asp481His)
c.2161G>C (p.Asp721His)
c.2311G>C (p.Asp771His)
c.2284G>C (p.Asp762His)
7g.150948987C>TCA369855199KCNH2n.3294G>A
c.2461G>A (p.Asp821Asn)
c.1441G>A (p.Asp481Asn)
c.2161G>A (p.Asp721Asn)
c.2311G>A (p.Asp771Asn)
c.2284G>A (p.Asp762Asn)
7g.150948988_150948990delCA2561770020KCNH2n.3292_3294del
c.2459_2461del (p.Gly820del)
c.1439_1441del (p.Gly480del)
c.2159_2161del (p.Gly720del)
c.2309_2311del (p.Gly770del)
c.2282_2284del (p.Gly761del)
7g.150948988C>ACA458645189KCNH2n.3293G>T
c.2460G>T (p.Gly820=)
c.1440G>T (p.Gly480=)
c.2160G>T (p.Gly720=)
c.2310G>T (p.Gly770=)
c.2283G>T (p.Gly761=)
7g.150948988C>GCA458645190KCNH2n.3293G>C
c.2460G>C (p.Gly820=)
c.1440G>C (p.Gly480=)
c.2160G>C (p.Gly720=)
c.2310G>C (p.Gly770=)
c.2283G>C (p.Gly761=)
 ClinVar gnomAD v4
7g.150948988C>TCA458645191KCNH2n.3293G>A
c.2460G>A (p.Gly820=)
c.1440G>A (p.Gly480=)
c.2160G>A (p.Gly720=)
c.2310G>A (p.Gly770=)
c.2283G>A (p.Gly761=)
 dbSNP
7g.150948989C>ACA369855201KCNH2n.3292G>T
c.2459G>T (p.Gly820Val)
c.1439G>T (p.Gly480Val)
c.2159G>T (p.Gly720Val)
c.2309G>T (p.Gly770Val)
c.2282G>T (p.Gly761Val)
7g.150948989C>GCA369855203KCNH2n.3292G>C
c.2459G>C (p.Gly820Ala)
c.1439G>C (p.Gly480Ala)
c.2159G>C (p.Gly720Ala)
c.2309G>C (p.Gly770Ala)
c.2282G>C (p.Gly761Ala)
7g.150948989C>TCA369855205KCNH2n.3292G>A
c.2459G>A (p.Gly820Glu)
c.1439G>A (p.Gly480Glu)
c.2159G>A (p.Gly720Glu)
c.2309G>A (p.Gly770Glu)
c.2282G>A (p.Gly761Glu)
 ClinVar gnomAD v4
7g.150948989_150948990insTAAAAAACA2567851703KCNH2n.3291_3292insTTTTTTA
c.2458_2459insTTTTTTA (p.Gly820ValfsTer3)
c.1438_1439insTTTTTTA (p.Gly480ValfsTer3)
c.2158_2159insTTTTTTA (p.Gly720ValfsTer3)
c.2308_2309insTTTTTTA (p.Gly770ValfsTer3)
c.2281_2282insTTTTTTA (p.Gly761ValfsTer3)
7g.150948989_150948990insAGGCCCTTGCATACACA2573141857KCNH2n.3291_3292insTGTATGCAAGGGCCT
c.2458_2459insTGTATGCAAGGGCCT (p.Gly820delinsValTyrAlaArgAlaTrp)
c.1438_1439insTGTATGCAAGGGCCT (p.Gly480delinsValTyrAlaArgAlaTrp)
c.2158_2159insTGTATGCAAGGGCCT (p.Gly720delinsValTyrAlaArgAlaTrp)
c.2308_2309insTGTATGCAAGGGCCT (p.Gly770delinsValTyrAlaArgAlaTrp)
c.2281_2282insTGTATGCAAGGGCCT (p.Gly761delinsValTyrAlaArgAlaTrp)
 ClinVar dbSNP
7g.150948990C>ACA369855207KCNH2n.3291G>T
c.2458G>T (p.Gly820Trp)
c.1438G>T (p.Gly480Trp)
c.2158G>T (p.Gly720Trp)
c.2308G>T (p.Gly770Trp)
c.2281G>T (p.Gly761Trp)
7g.150948990C=CA1752432024KCNH2n.3291G=
c.2458G= (p.Gly820=)
c.1438G= (p.Gly480=)
c.2158G= (p.Gly720=)
c.2308G= (p.Gly770=)
c.2281G= (p.Gly761=)
7g.150948990C>GCA369855209KCNH2n.3291G>C
c.2458G>C (p.Gly820Arg)
c.1438G>C (p.Gly480Arg)
c.2158G>C (p.Gly720Arg)
c.2308G>C (p.Gly770Arg)
c.2281G>C (p.Gly761Arg)
 ClinVar
7g.150948990C>TCA006787KCNH2n.3291G>A
c.2458G>A (p.Gly820Arg)
c.1438G>A (p.Gly480Arg)
c.2158G>A (p.Gly720Arg)
c.2308G>A (p.Gly770Arg)
c.2281G>A (p.Gly761Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
7g.150948991G>ACA032843KCNH2n.3290C>T
c.2457C>T (p.Asn819=)
c.1437C>T (p.Asn479=)
c.2157C>T (p.Asn719=)
c.2307C>T (p.Asn769=)
c.2280C>T (p.Asn760=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.150948991G>CCA169074833KCNH2n.3290C>G
c.2457C>G (p.Asn819Lys)
c.1437C>G (p.Asn479Lys)
c.2157C>G (p.Asn719Lys)
c.2307C>G (p.Asn769Lys)
c.2280C>G (p.Asn760Lys)
 ClinVar dbSNP
7g.150948991G=CA1752432026KCNH2n.3290C=
c.2457C= (p.Asn819=)
c.1437C= (p.Asn479=)
c.2157C= (p.Asn719=)
c.2307C= (p.Asn769=)
c.2280C= (p.Asn760=)
7g.150948991G>TCA369855213KCNH2n.3290C>A
c.2457C>A (p.Asn819Lys)
c.1437C>A (p.Asn479Lys)
c.2157C>A (p.Asn719Lys)
c.2307C>A (p.Asn769Lys)
c.2280C>A (p.Asn760Lys)
 dbSNP gnomAD v3 gnomAD v4
7g.150948991_150948992delinsGTCA1752432030KCNH2n.3289_3290delinsAC
c.2456_2457delinsAC (p.Asn819=)
c.1436_1437delinsAC (p.Asn479=)
c.2156_2157delinsAC (p.Asn719=)
c.2306_2307delinsAC (p.Asn769=)
c.2279_2280delinsAC (p.Asn760=)
7g.150948992T>ACA369855219KCNH2n.3289A>T
c.2456A>T (p.Asn819Ile)
c.1436A>T (p.Asn479Ile)
c.2156A>T (p.Asn719Ile)
c.2306A>T (p.Asn769Ile)
c.2279A>T (p.Asn760Ile)
7g.150948992T>CCA369855221KCNH2n.3289A>G
c.2456A>G (p.Asn819Ser)
c.1436A>G (p.Asn479Ser)
c.2156A>G (p.Asn719Ser)
c.2306A>G (p.Asn769Ser)
c.2279A>G (p.Asn760Ser)
7g.150948992T>GCA369855217KCNH2n.3289A>C
c.2456A>C (p.Asn819Thr)
c.1436A>C (p.Asn479Thr)
c.2156A>C (p.Asn719Thr)
c.2306A>C (p.Asn769Thr)
c.2279A>C (p.Asn760Thr)
7g.150948993delCA006779KCNH2n.3289del
c.2456del (p.Asn819ThrfsTer?)
c.1436del (p.Asn479ThrfsTer?)
c.2156del (p.Asn719ThrfsTer?)
c.2306del (p.Asn769ThrfsTer?)
c.2279del (p.Asn760ThrfsTer?)
 ClinVar dbSNP
7g.150948993T>ACA369855223KCNH2n.3288A>T
c.2455A>T (p.Asn819Tyr)
c.1435A>T (p.Asn479Tyr)
c.2155A>T (p.Asn719Tyr)
c.2305A>T (p.Asn769Tyr)
c.2278A>T (p.Asn760Tyr)
7g.150948993T>CCA369855225KCNH2n.3288A>G
c.2455A>G (p.Asn819Asp)
c.1435A>G (p.Asn479Asp)
c.2155A>G (p.Asn719Asp)
c.2305A>G (p.Asn769Asp)
c.2278A>G (p.Asn760Asp)
7g.150948993T>GCA369855227KCNH2n.3288A>C
c.2455A>C (p.Asn819His)
c.1435A>C (p.Asn479His)
c.2155A>C (p.Asn719His)
c.2305A>C (p.Asn769His)
c.2278A>C (p.Asn760His)
7g.150948994C>ACA169074843KCNH2n.3287G>T
c.2454G>T (p.Ser818=)
c.1434G>T (p.Ser478=)
c.2154G>T (p.Ser718=)
c.2304G>T (p.Ser768=)
c.2277G>T (p.Ser759=)
 dbSNP
7g.150948994C=CA1752432035KCNH2n.3287G=
c.2454G= (p.Ser818=)
c.1434G= (p.Ser478=)
c.2154G= (p.Ser718=)
c.2304G= (p.Ser768=)
c.2277G= (p.Ser759=)
7g.150948994C>GCA032829KCNH2n.3287G>C
c.2454G>C (p.Ser818=)
c.1434G>C (p.Ser478=)
c.2154G>C (p.Ser718=)
c.2304G>C (p.Ser768=)
c.2277G>C (p.Ser759=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.150948994C>TCA006771KCNH2n.3287G>A
c.2454G>A (p.Ser818=)
c.1434G>A (p.Ser478=)
c.2154G>A (p.Ser718=)
c.2304G>A (p.Ser768=)
c.2277G>A (p.Ser759=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.150948995G>ACA006763KCNH2n.3286C>T
c.2453C>T (p.Ser818Leu)
c.1433C>T (p.Ser478Leu)
c.2153C>T (p.Ser718Leu)
c.2303C>T (p.Ser768Leu)
c.2276C>T (p.Ser759Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.150948995G>CCA369855233KCNH2n.3286C>G
c.2453C>G (p.Ser818Trp)
c.1433C>G (p.Ser478Trp)
c.2153C>G (p.Ser718Trp)
c.2303C>G (p.Ser768Trp)
c.2276C>G (p.Ser759Trp)
 ClinVar COSMIC
7g.150948995G=CA1752432041KCNH2n.3286C=
c.2453C= (p.Ser818=)
c.1433C= (p.Ser478=)
c.2153C= (p.Ser718=)
c.2303C= (p.Ser768=)
c.2276C= (p.Ser759=)
7g.150948995G>TCA369855235KCNH2n.3286C>A
c.2453C>A (p.Ser818Ter)
c.1433C>A (p.Ser478Ter)
c.2153C>A (p.Ser718Ter)
c.2303C>A (p.Ser768Ter)
c.2276C>A (p.Ser759Ter)
7g.150948996A=CA1752432044KCNH2n.3285T=
c.2452T= (p.Ser818=)
c.1432T= (p.Ser478=)
c.2152T= (p.Ser718=)
c.2302T= (p.Ser768=)
c.2275T= (p.Ser759=)
7g.150948996A>CCA369855238KCNH2n.3285T>G
c.2452T>G (p.Ser818Ala)
c.1432T>G (p.Ser478Ala)
c.2152T>G (p.Ser718Ala)
c.2302T>G (p.Ser768Ala)
c.2275T>G (p.Ser759Ala)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150948996A>GCA006757KCNH2n.3285T>C
c.2452T>C (p.Ser818Pro)
c.1432T>C (p.Ser478Pro)
c.2152T>C (p.Ser718Pro)
c.2302T>C (p.Ser768Pro)
c.2275T>C (p.Ser759Pro)
 ClinVar dbSNP
7g.150948996A>TCA369855240KCNH2n.3285T>A
c.2452T>A (p.Ser818Thr)
c.1432T>A (p.Ser478Thr)
c.2152T>A (p.Ser718Thr)
c.2302T>A (p.Ser768Thr)
c.2275T>A (p.Ser759Thr)
7g.150948996_150949006delinsACTTGCCAGGCCA1752432047KCNH2n.3275_3285delinsGCCTGGCAAGT
c.2442_2452delinsGCCTGGCAAGT (p.Arg814=)
c.1422_1432delinsGCCTGGCAAGT (p.Arg474=)
c.2142_2152delinsGCCTGGCAAGT (p.Arg714=)
c.2292_2302delinsGCCTGGCAAGT (p.Arg764=)
c.2265_2275delinsGCCTGGCAAGT (p.Arg755=)
7g.150948997C>ACA369855243KCNH2n.3284G>T
c.2451G>T (p.Lys817Asn)
c.1431G>T (p.Lys477Asn)
c.2151G>T (p.Lys717Asn)
c.2301G>T (p.Lys767Asn)
c.2274G>T (p.Lys758Asn)
7g.150948997C>GCA369855245KCNH2n.3284G>C
c.2451G>C (p.Lys817Asn)
c.1431G>C (p.Lys477Asn)
c.2151G>C (p.Lys717Asn)
c.2301G>C (p.Lys767Asn)
c.2274G>C (p.Lys758Asn)
7g.150948997C>TCA458645192KCNH2n.3284G>A
c.2451G>A (p.Lys817=)
c.1431G>A (p.Lys477=)
c.2151G>A (p.Lys717=)
c.2301G>A (p.Lys767=)
c.2274G>A (p.Lys758=)
7g.150949002_150949011delCA658797040KCNH2n.3275_3284del
c.2442_2451del (p.Arg814SerfsTer?)
c.1422_1431del (p.Arg474SerfsTer?)
c.2142_2151del (p.Arg714SerfsTer?)
c.2292_2301del (p.Arg764SerfsTer?)
c.2265_2274del (p.Arg755SerfsTer?)
 ClinVar dbSNP
7g.150948998T>ACA369855251KCNH2n.3283A>T
c.2450A>T (p.Lys817Met)
c.1430A>T (p.Lys477Met)
c.2150A>T (p.Lys717Met)
c.2300A>T (p.Lys767Met)
c.2273A>T (p.Lys758Met)
7g.150948998T>CCA369855247KCNH2n.3283A>G
c.2450A>G (p.Lys817Arg)
c.1430A>G (p.Lys477Arg)
c.2150A>G (p.Lys717Arg)
c.2300A>G (p.Lys767Arg)
c.2273A>G (p.Lys758Arg)
 COSMIC COSMIC
7g.150948998T>GCA369855249KCNH2n.3283A>C
c.2450A>C (p.Lys817Thr)
c.1430A>C (p.Lys477Thr)
c.2150A>C (p.Lys717Thr)
c.2300A>C (p.Lys767Thr)
c.2273A>C (p.Lys758Thr)
7g.150948999T>ACA369855253KCNH2n.3282A>T
c.2449A>T (p.Lys817Ter)
c.1429A>T (p.Lys477Ter)
c.2149A>T (p.Lys717Ter)
c.2299A>T (p.Lys767Ter)
c.2272A>T (p.Lys758Ter)
7g.150948999T>CCA369855254KCNH2n.3282A>G
c.2449A>G (p.Lys817Glu)
c.1429A>G (p.Lys477Glu)
c.2149A>G (p.Lys717Glu)
c.2299A>G (p.Lys767Glu)
c.2272A>G (p.Lys758Glu)
7g.150948999T>GCA369855255KCNH2n.3282A>C
c.2449A>C (p.Lys817Gln)
c.1429A>C (p.Lys477Gln)
c.2149A>C (p.Lys717Gln)
c.2299A>C (p.Lys767Gln)
c.2272A>C (p.Lys758Gln)
7g.150949000G>ACA458645193KCNH2n.3281C>T
c.2448C>T (p.Gly816=)
c.1428C>T (p.Gly476=)
c.2148C>T (p.Gly716=)
c.2298C>T (p.Gly766=)
c.2271C>T (p.Gly757=)
7g.150949000G>CCA169074886KCNH2n.3281C>G
c.2448C>G (p.Gly816=)
c.1428C>G (p.Gly476=)
c.2148C>G (p.Gly716=)
c.2298C>G (p.Gly766=)
c.2271C>G (p.Gly757=)
 ClinVar dbSNP gnomAD v4
7g.150949000G=CA1752432052KCNH2n.3281C=
c.2448C= (p.Gly816=)
c.1428C= (p.Gly476=)
c.2148C= (p.Gly716=)
c.2298C= (p.Gly766=)
c.2271C= (p.Gly757=)
7g.150949000G>TCA458645194KCNH2n.3281C>A
c.2448C>A (p.Gly816=)
c.1428C>A (p.Gly476=)
c.2148C>A (p.Gly716=)
c.2298C>A (p.Gly766=)
c.2271C>A (p.Gly757=)
7g.150949001C>ACA369855258KCNH2n.3280G>T
c.2447G>T (p.Gly816Val)
c.1427G>T (p.Gly476Val)
c.2147G>T (p.Gly716Val)
c.2297G>T (p.Gly766Val)
c.2270G>T (p.Gly757Val)
7g.150949001C>GCA369855259KCNH2n.3280G>C
c.2447G>C (p.Gly816Ala)
c.1427G>C (p.Gly476Ala)
c.2147G>C (p.Gly716Ala)
c.2297G>C (p.Gly766Ala)
c.2270G>C (p.Gly757Ala)
7g.150949001C>TCA369855260KCNH2n.3280G>A
c.2447G>A (p.Gly816Asp)
c.1427G>A (p.Gly476Asp)
c.2147G>A (p.Gly716Asp)
c.2297G>A (p.Gly766Asp)
c.2270G>A (p.Gly757Asp)
7g.150949002C>ACA369855262KCNH2n.3279G>T
c.2446G>T (p.Gly816Cys)
c.1426G>T (p.Gly476Cys)
c.2146G>T (p.Gly716Cys)
c.2296G>T (p.Gly766Cys)
c.2269G>T (p.Gly757Cys)
7g.150949002C>GCA369855266KCNH2n.3279G>C
c.2446G>C (p.Gly816Arg)
c.1426G>C (p.Gly476Arg)
c.2146G>C (p.Gly716Arg)
c.2296G>C (p.Gly766Arg)
c.2269G>C (p.Gly757Arg)
7g.150949002C>TCA369855264KCNH2n.3279G>A
c.2446G>A (p.Gly816Ser)
c.1426G>A (p.Gly476Ser)
c.2146G>A (p.Gly716Ser)
c.2296G>A (p.Gly766Ser)
c.2269G>A (p.Gly757Ser)
7g.150949003A=CA1752432055KCNH2n.3278T=
c.2445T= (p.Pro815=)
c.1425T= (p.Pro475=)
c.2145T= (p.Pro715=)
c.2295T= (p.Pro765=)
c.2268T= (p.Pro756=)
7g.150949003A>CCA458645195KCNH2n.3278T>G
c.2445T>G (p.Pro815=)
c.1425T>G (p.Pro475=)
c.2145T>G (p.Pro715=)
c.2295T>G (p.Pro765=)
c.2268T>G (p.Pro756=)
7g.150949003A>GCA032754KCNH2n.3278T>C
c.2445T>C (p.Pro815=)
c.1425T>C (p.Pro475=)
c.2145T>C (p.Pro715=)
c.2295T>C (p.Pro765=)
c.2268T>C (p.Pro756=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.150949003A>TCA458645196KCNH2n.3278T>A
c.2445T>A (p.Pro815=)
c.1425T>A (p.Pro475=)
c.2145T>A (p.Pro715=)
c.2295T>A (p.Pro765=)
c.2268T>A (p.Pro756=)
7g.150949004G>ACA369855270KCNH2n.3277C>T
c.2444C>T (p.Pro815Leu)
c.1424C>T (p.Pro475Leu)
c.2144C>T (p.Pro715Leu)
c.2294C>T (p.Pro765Leu)
c.2267C>T (p.Pro756Leu)
7g.150949004G>CCA369855271KCNH2n.3277C>G
c.2444C>G (p.Pro815Arg)
c.1424C>G (p.Pro475Arg)
c.2144C>G (p.Pro715Arg)
c.2294C>G (p.Pro765Arg)
c.2267C>G (p.Pro756Arg)
7g.150949004G>TCA369855274KCNH2n.3277C>A
c.2444C>A (p.Pro815His)
c.1424C>A (p.Pro475His)
c.2144C>A (p.Pro715His)
c.2294C>A (p.Pro765His)
c.2267C>A (p.Pro756His)
7g.150949005G>ACA369855276KCNH2n.3276C>T
c.2443C>T (p.Pro815Ser)
c.1423C>T (p.Pro475Ser)
c.2143C>T (p.Pro715Ser)
c.2293C>T (p.Pro765Ser)
c.2266C>T (p.Pro756Ser)
7g.150949005G>CCA369855280KCNH2n.3276C>G
c.2443C>G (p.Pro815Ala)
c.1423C>G (p.Pro475Ala)
c.2143C>G (p.Pro715Ala)
c.2293C>G (p.Pro765Ala)
c.2266C>G (p.Pro756Ala)
 ClinVar
7g.150949005G>TCA369855278KCNH2n.3276C>A
c.2443C>A (p.Pro815Thr)
c.1423C>A (p.Pro475Thr)
c.2143C>A (p.Pro715Thr)
c.2293C>A (p.Pro765Thr)
c.2266C>A (p.Pro756Thr)
7g.150949006C>ACA369855282KCNH2n.3275G>T
c.2442G>T (p.Arg814Ser)
c.1422G>T (p.Arg474Ser)
c.2142G>T (p.Arg714Ser)
c.2292G>T (p.Arg764Ser)
c.2265G>T (p.Arg755Ser)
7g.150949006C>GCA369855284KCNH2n.3275G>C
c.2442G>C (p.Arg814Ser)
c.1422G>C (p.Arg474Ser)
c.2142G>C (p.Arg714Ser)
c.2292G>C (p.Arg764Ser)
c.2265G>C (p.Arg755Ser)
7g.150949006C>TCA458645197KCNH2n.3275G>A
c.2442G>A (p.Arg814=)
c.1422G>A (p.Arg474=)
c.2142G>A (p.Arg714=)
c.2292G>A (p.Arg764=)
c.2265G>A (p.Arg755=)
7g.150949007C>ACA369855286KCNH2n.3274G>T
c.2441G>T (p.Arg814Met)
c.1421G>T (p.Arg474Met)
c.2141G>T (p.Arg714Met)
c.2291G>T (p.Arg764Met)
c.2264G>T (p.Arg755Met)
 dbSNP
7g.150949007C>GCA369855288KCNH2n.3274G>C
c.2441G>C (p.Arg814Thr)
c.1421G>C (p.Arg474Thr)
c.2141G>C (p.Arg714Thr)
c.2291G>C (p.Arg764Thr)
c.2264G>C (p.Arg755Thr)
7g.150949007C>TCA369855290KCNH2n.3274G>A
c.2441G>A (p.Arg814Lys)
c.1421G>A (p.Arg474Lys)
c.2141G>A (p.Arg714Lys)
c.2291G>A (p.Arg764Lys)
c.2264G>A (p.Arg755Lys)
 ClinVar gnomAD v4
7g.150949008T>ACA369855292KCNH2n.3273A>T
c.2440A>T (p.Arg814Trp)
c.1420A>T (p.Arg474Trp)
c.2140A>T (p.Arg714Trp)
c.2290A>T (p.Arg764Trp)
c.2263A>T (p.Arg755Trp)
7g.150949008T>CCA369855294KCNH2n.3273A>G
c.2440A>G (p.Arg814Gly)
c.1420A>G (p.Arg474Gly)
c.2140A>G (p.Arg714Gly)
c.2290A>G (p.Arg764Gly)
c.2263A>G (p.Arg755Gly)
7g.150949008T>GCA458645198KCNH2n.3273A>C
c.2440A>C (p.Arg814=)
c.1420A>C (p.Arg474=)
c.2140A>C (p.Arg714=)
c.2290A>C (p.Arg764=)
c.2263A>C (p.Arg755=)
7g.150949009T>ACA458645199KCNH2n.3272A>T
c.2439A>T (p.Ala813=)
c.1419A>T (p.Ala473=)
c.2139A>T (p.Ala713=)
c.2289A>T (p.Ala763=)
c.2262A>T (p.Ala754=)
7g.150949009T>CCA458645201KCNH2n.3272A>G
c.2439A>G (p.Ala813=)
c.1419A>G (p.Ala473=)
c.2139A>G (p.Ala713=)
c.2289A>G (p.Ala763=)
c.2262A>G (p.Ala754=)
7g.150949009T>GCA458645200KCNH2n.3272A>C
c.2439A>C (p.Ala813=)
c.1419A>C (p.Ala473=)
c.2139A>C (p.Ala713=)
c.2289A>C (p.Ala763=)
c.2262A>C (p.Ala754=)
7g.150949010G>ACA369855296KCNH2n.3271C>T
c.2438C>T (p.Ala813Val)
c.1418C>T (p.Ala473Val)
c.2138C>T (p.Ala713Val)
c.2288C>T (p.Ala763Val)
c.2261C>T (p.Ala754Val)
 dbSNP
7g.150949010G>CCA369855298KCNH2n.3271C>G
c.2438C>G (p.Ala813Gly)
c.1418C>G (p.Ala473Gly)
c.2138C>G (p.Ala713Gly)
c.2288C>G (p.Ala763Gly)
c.2261C>G (p.Ala754Gly)
 ClinVar gnomAD v4
7g.150949010G=CA1752432059KCNH2n.3271C=
c.2438C= (p.Ala813=)
c.1418C= (p.Ala473=)
c.2138C= (p.Ala713=)
c.2288C= (p.Ala763=)
c.2261C= (p.Ala754=)
7g.150949010G>TCA369855300KCNH2n.3271C>A
c.2438C>A (p.Ala813Glu)
c.1418C>A (p.Ala473Glu)
c.2138C>A (p.Ala713Glu)
c.2288C>A (p.Ala763Glu)
c.2261C>A (p.Ala754Glu)
7g.150949011C>ACA369855302KCNH2n.3270G>T
c.2437G>T (p.Ala813Ser)
c.1417G>T (p.Ala473Ser)
c.2137G>T (p.Ala713Ser)
c.2287G>T (p.Ala763Ser)
c.2260G>T (p.Ala754Ser)
7g.150949011C=CA1752432062KCNH2n.3270G=
c.2437G= (p.Ala813=)
c.1417G= (p.Ala473=)
c.2137G= (p.Ala713=)
c.2287G= (p.Ala763=)
c.2260G= (p.Ala754=)
7g.150949011C>GCA369855304KCNH2n.3270G>C
c.2437G>C (p.Ala813Pro)
c.1417G>C (p.Ala473Pro)
c.2137G>C (p.Ala713Pro)
c.2287G>C (p.Ala763Pro)
c.2260G>C (p.Ala754Pro)
7g.150949011C>TCA369855306KCNH2n.3270G>A
c.2437G>A (p.Ala813Thr)
c.1417G>A (p.Ala473Thr)
c.2137G>A (p.Ala713Thr)
c.2287G>A (p.Ala763Thr)
c.2260G>A (p.Ala754Thr)
 ClinVar dbSNP
7g.150949012A=CA1752432063KCNH2n.3269T=
c.2436T= (p.Tyr812=)
c.1416T= (p.Tyr472=)
c.2136T= (p.Tyr712=)
c.2286T= (p.Tyr762=)
c.2259T= (p.Tyr753=)
7g.150949012A>CCA369855310KCNH2n.3269T>G
c.2436T>G (p.Tyr812Ter)
c.1416T>G (p.Tyr472Ter)
c.2136T>G (p.Tyr712Ter)
c.2286T>G (p.Tyr762Ter)
c.2259T>G (p.Tyr753Ter)
7g.150949012A>GCA458645202KCNH2n.3269T>C
c.2436T>C (p.Tyr812=)
c.1416T>C (p.Tyr472=)
c.2136T>C (p.Tyr712=)
c.2286T>C (p.Tyr762=)
c.2259T>C (p.Tyr753=)
 dbSNP
7g.150949012A>TCA369855308KCNH2n.3269T>A
c.2436T>A (p.Tyr812Ter)
c.1416T>A (p.Tyr472Ter)
c.2136T>A (p.Tyr712Ter)
c.2286T>A (p.Tyr762Ter)
c.2259T>A (p.Tyr753Ter)
 ClinVar dbSNP
7g.150949012dupCA2695208829KCNH2n.3269dup
c.2436dup (p.Ala813CysfsTer17)
c.1416dup (p.Ala473CysfsTer17)
c.2136dup (p.Ala713CysfsTer17)
c.2286dup (p.Ala763CysfsTer17)
c.2259dup (p.Ala754CysfsTer17)
7g.150949013T>ACA369855313KCNH2n.3268A>T
c.2435A>T (p.Tyr812Phe)
c.1415A>T (p.Tyr472Phe)
c.2135A>T (p.Tyr712Phe)
c.2285A>T (p.Tyr762Phe)
c.2258A>T (p.Tyr753Phe)
7g.150949013T>CCA369855314KCNH2n.3268A>G
c.2435A>G (p.Tyr812Cys)
c.1415A>G (p.Tyr472Cys)
c.2135A>G (p.Tyr712Cys)
c.2285A>G (p.Tyr762Cys)
c.2258A>G (p.Tyr753Cys)
 ClinVar dbSNP
7g.150949013T>GCA369855316KCNH2n.3268A>C
c.2435A>C (p.Tyr812Ser)
c.1415A>C (p.Tyr472Ser)
c.2135A>C (p.Tyr712Ser)
c.2285A>C (p.Tyr762Ser)
c.2258A>C (p.Tyr753Ser)
 dbSNP gnomAD v2 gnomAD v4
7g.150949013T=CA1752432067KCNH2n.3268A=
c.2435A= (p.Tyr812=)
c.1415A= (p.Tyr472=)
c.2135A= (p.Tyr712=)
c.2285A= (p.Tyr762=)
c.2258A= (p.Tyr753=)
7g.150949014A>CCA369855319KCNH2n.3267T>G
c.2434T>G (p.Tyr812Asp)
c.1414T>G (p.Tyr472Asp)
c.2134T>G (p.Tyr712Asp)
c.2284T>G (p.Tyr762Asp)
c.2257T>G (p.Tyr753Asp)
7g.150949014A>GCA369855320KCNH2n.3267T>C
c.2434T>C (p.Tyr812His)
c.1414T>C (p.Tyr472His)
c.2134T>C (p.Tyr712His)
c.2284T>C (p.Tyr762His)
c.2257T>C (p.Tyr753His)
7g.150949014A>TCA369855321KCNH2n.3267T>A
c.2434T>A (p.Tyr812Asn)
c.1414T>A (p.Tyr472Asn)
c.2134T>A (p.Tyr712Asn)
c.2284T>A (p.Tyr762Asn)
c.2257T>A (p.Tyr753Asn)
7g.150949015C>ACA458645203KCNH2n.3266G>T
c.2433G>T (p.Leu811=)
c.1413G>T (p.Leu471=)
c.2133G>T (p.Leu711=)
c.2283G>T (p.Leu761=)
c.2256G>T (p.Leu752=)
 dbSNP
7g.150949015C=CA1752432069KCNH2n.3266G=
c.2433G= (p.Leu811=)
c.1413G= (p.Leu471=)
c.2133G= (p.Leu711=)
c.2283G= (p.Leu761=)
c.2256G= (p.Leu752=)
7g.150949015C>GCA458645205KCNH2n.3266G>C
c.2433G>C (p.Leu811=)
c.1413G>C (p.Leu471=)
c.2133G>C (p.Leu711=)
c.2283G>C (p.Leu761=)
c.2256G>C (p.Leu752=)
7g.150949015C>TCA458645204KCNH2n.3266G>A
c.2433G>A (p.Leu811=)
c.1413G>A (p.Leu471=)
c.2133G>A (p.Leu711=)
c.2283G>A (p.Leu761=)
c.2256G>A (p.Leu752=)
 ClinVar dbSNP gnomAD v4
7g.150949016A=CA1752432070KCNH2n.3265T=
c.2432T= (p.Leu811=)
c.1412T= (p.Leu471=)
c.2132T= (p.Leu711=)
c.2282T= (p.Leu761=)
c.2255T= (p.Leu752=)
7g.150949016A>CCA369855323KCNH2n.3265T>G
c.2432T>G (p.Leu811Arg)
c.1412T>G (p.Leu471Arg)
c.2132T>G (p.Leu711Arg)
c.2282T>G (p.Leu761Arg)
c.2255T>G (p.Leu752Arg)
7g.150949016A>GCA369855326KCNH2n.3265T>C
c.2432T>C (p.Leu811Pro)
c.1412T>C (p.Leu471Pro)
c.2132T>C (p.Leu711Pro)
c.2282T>C (p.Leu761Pro)
c.2255T>C (p.Leu752Pro)
 dbSNP
7g.150949016A>TCA369855328KCNH2n.3265T>A
c.2432T>A (p.Leu811Gln)
c.1412T>A (p.Leu471Gln)
c.2132T>A (p.Leu711Gln)
c.2282T>A (p.Leu761Gln)
c.2255T>A (p.Leu752Gln)
7g.150949017G>ACA458645206KCNH2n.3264C>T
c.2431C>T (p.Leu811=)
c.1411C>T (p.Leu471=)
c.2131C>T (p.Leu711=)
c.2281C>T (p.Leu761=)
c.2254C>T (p.Leu752=)
 gnomAD v4
7g.150949017G>CCA369855330KCNH2n.3264C>G
c.2431C>G (p.Leu811Val)
c.1411C>G (p.Leu471Val)
c.2131C>G (p.Leu711Val)
c.2281C>G (p.Leu761Val)
c.2254C>G (p.Leu752Val)
7g.150949017G>TCA369855331KCNH2n.3264C>A
c.2431C>A (p.Leu811Met)
c.1411C>A (p.Leu471Met)
c.2131C>A (p.Leu711Met)
c.2281C>A (p.Leu761Met)
c.2254C>A (p.Leu752Met)
7g.150949018G>ACA458645207KCNH2n.3263C>T
c.2430C>T (p.Asn810=)
c.1410C>T (p.Asn470=)
c.2130C>T (p.Asn710=)
c.2280C>T (p.Asn760=)
c.2253C>T (p.Asn751=)
 ClinVar
7g.150949018G>CCA169074887KCNH2n.3263C>G
c.2430C>G (p.Asn810Lys)
c.1410C>G (p.Asn470Lys)
c.2130C>G (p.Asn710Lys)
c.2280C>G (p.Asn760Lys)
c.2253C>G (p.Asn751Lys)
 dbSNP
7g.150949018G=CA1752432072KCNH2n.3263C=
c.2430C= (p.Asn810=)
c.1410C= (p.Asn470=)
c.2130C= (p.Asn710=)
c.2280C= (p.Asn760=)
c.2253C= (p.Asn751=)
7g.150949018G>TCA369855335KCNH2n.3263C>A
c.2430C>A (p.Asn810Lys)
c.1410C>A (p.Asn470Lys)
c.2130C>A (p.Asn710Lys)
c.2280C>A (p.Asn760Lys)
c.2253C>A (p.Asn751Lys)

Number of alleles fetched