Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.130997613_130997614delCA2586965906ATP2C1c.2251_2252del (p.Val751ArgfsTer5)
c.2236_2237del (p.Val746ArgfsTer5)
c.2112_2113del
c.2203_2204del (p.Val735ArgfsTer5)
c.2353_2354del (p.Val785ArgfsTer5)
c.150_151del (p.Ter51GluextTer?)
c.804_805del
n.2421_2422del
c.2182_2183del (p.Val728ArgfsTer5)
c.1417_1418del (p.Val473ArgfsTer5)
3g.130997614T>ACA354536960ATP2C1c.2252T>A (p.Val751Glu)
c.2237T>A (p.Val746Glu)
c.2113T>A
c.2204T>A (p.Val735Glu)
c.2354T>A (p.Val785Glu)
c.151T>A (p.Ter51Lys)
c.805T>A
n.2422T>A
c.2183T>A (p.Val728Glu)
c.1418T>A (p.Val473Glu)
3g.130997614T>CCA354536962ATP2C1c.2252T>C (p.Val751Ala)
c.2237T>C (p.Val746Ala)
c.2113T>C
c.2204T>C (p.Val735Ala)
c.2354T>C (p.Val785Ala)
c.151T>C (p.Ter51Gln)
c.805T>C
n.2422T>C
c.2183T>C (p.Val728Ala)
c.1418T>C (p.Val473Ala)
gnomAD v4
3g.130997614T>GCA354536964ATP2C1c.2252T>G (p.Val751Gly)
c.2237T>G (p.Val746Gly)
c.2113T>G
c.2204T>G (p.Val735Gly)
c.2354T>G (p.Val785Gly)
c.151T>G (p.Ter51Glu)
c.805T>G
n.2422T>G
c.2183T>G (p.Val728Gly)
c.1418T>G (p.Val473Gly)
3g.130997615A=CA1401883562ATP2C1c.2253A= (p.Val751=)
c.2238A= (p.Val746=)
c.2114A=
c.2205A= (p.Val735=)
c.2355A= (p.Val785=)
c.152A= (p.Ter51=)
c.806A=
n.2423A=
c.2184A= (p.Val728=)
c.1419A= (p.Val473=)
3g.130997615A>CCA435662217ATP2C1c.2253A>C (p.Val751=)
c.2238A>C (p.Val746=)
c.2114A>C
c.2205A>C (p.Val735=)
c.2355A>C (p.Val785=)
c.152A>C (p.Ter51Ser)
c.806A>C
n.2423A>C
c.2184A>C (p.Val728=)
c.1419A>C (p.Val473=)
3g.130997615A>GCA83503984ATP2C1c.2253A>G (p.Val751=)
c.2238A>G (p.Val746=)
c.2114A>G
c.2205A>G (p.Val735=)
c.2355A>G (p.Val785=)
c.152A>G (p.Ter51Trp)
c.806A>G
n.2423A>G
c.2184A>G (p.Val728=)
c.1419A>G (p.Val473=)
dbSNP
3g.130997615A>TCA435662220ATP2C1c.2253A>T (p.Val751=)
c.2238A>T (p.Val746=)
c.2114A>T
c.2205A>T (p.Val735=)
c.2355A>T (p.Val785=)
c.152A>T (p.Ter51Leu)
c.806A>T
n.2423A>T
c.2184A>T (p.Val728=)
c.1419A>T (p.Val473=)
3g.130997616G>ACA354536968ATP2C1c.2254G>A (p.Glu752Lys)
c.2239G>A (p.Glu747Lys)
c.2115G>A
c.2206G>A (p.Glu736Lys)
c.2356G>A (p.Glu786Lys)
c.153G>A (p.Ter51=)
c.807G>A
n.2424G>A
c.2185G>A (p.Glu729Lys)
c.1420G>A (p.Glu474Lys)
3g.130997616G>CCA354536970ATP2C1c.2254G>C (p.Glu752Gln)
c.2239G>C (p.Glu747Gln)
c.2115G>C
c.2206G>C (p.Glu736Gln)
c.2356G>C (p.Glu786Gln)
c.153G>C (p.Ter51Tyr)
c.807G>C
n.2424G>C
c.2185G>C (p.Glu729Gln)
c.1420G>C (p.Glu474Gln)
3g.130997616G>TCA354536972ATP2C1c.2254G>T (p.Glu752Ter)
c.2239G>T (p.Glu747Ter)
c.2115G>T
c.2206G>T (p.Glu736Ter)
c.2356G>T (p.Glu786Ter)
c.153G>T (p.Ter51Tyr)
c.807G>T
n.2424G>T
c.2185G>T (p.Glu729Ter)
c.1420G>T (p.Glu474Ter)
3g.130997617A>CCA354536977ATP2C1c.2255A>C (p.Glu752Ala)
c.2240A>C (p.Glu747Ala)
c.2116A>C
c.2207A>C (p.Glu736Ala)
c.2357A>C (p.Glu786Ala)
c.154A>C (n.154A>C)
c.808A>C
n.2425A>C
c.2186A>C (p.Glu729Ala)
c.1421A>C (p.Glu474Ala)
3g.130997617A>GCA354536980ATP2C1c.2255A>G (p.Glu752Gly)
c.2240A>G (p.Glu747Gly)
c.2116A>G
c.2207A>G (p.Glu736Gly)
c.2357A>G (p.Glu786Gly)
c.154A>G (n.154A>G)
c.808A>G
n.2425A>G
c.2186A>G (p.Glu729Gly)
c.1421A>G (p.Glu474Gly)
3g.130997617A>TCA354536976ATP2C1c.2255A>T (p.Glu752Val)
c.2240A>T (p.Glu747Val)
c.2116A>T
c.2207A>T (p.Glu736Val)
c.2357A>T (p.Glu786Val)
c.154A>T (n.154A>T)
c.808A>T
n.2425A>T
c.2186A>T (p.Glu729Val)
c.1421A>T (p.Glu474Val)
3g.130997618_130997621delCA2580068759ATP2C1c.2256_2259del (p.Pro753TrpfsTer18)
c.2241_2244del (p.Pro748TrpfsTer18)
c.2117_2120del
c.2208_2211del (p.Pro737TrpfsTer18)
c.2358_2361del (p.Pro787TrpfsTer18)
c.155_158del (n.155_158del)
c.809_812del
n.2426_2429del
c.2187_2190del (p.Pro730TrpfsTer18)
c.1422_1425del (p.Pro475TrpfsTer18)
ClinVar
3g.130997618A=CA1401883564ATP2C1c.2256A= (p.Glu752=)
c.2241A= (p.Glu747=)
c.2117A=
c.2208A= (p.Glu736=)
c.2358A= (p.Glu786=)
c.155A= (n.155A=)
c.809A=
n.2426A=
c.2187A= (p.Glu729=)
c.1422A= (p.Glu474=)
3g.130997618A>CCA354536983ATP2C1c.2256A>C (p.Glu752Asp)
c.2241A>C (p.Glu747Asp)
c.2117A>C
c.2208A>C (p.Glu736Asp)
c.2358A>C (p.Glu786Asp)
c.155A>C (n.155A>C)
c.809A>C
n.2426A>C
c.2187A>C (p.Glu729Asp)
c.1422A>C (p.Glu474Asp)
3g.130997618A>GCA435662222ATP2C1c.2256A>G (p.Glu752=)
c.2241A>G (p.Glu747=)
c.2117A>G
c.2208A>G (p.Glu736=)
c.2358A>G (p.Glu786=)
c.155A>G (n.155A>G)
c.809A>G
n.2426A>G
c.2187A>G (p.Glu729=)
c.1422A>G (p.Glu474=)
dbSNP gnomAD v2 gnomAD v4
3g.130997618A>TCA354536985ATP2C1c.2256A>T (p.Glu752Asp)
c.2241A>T (p.Glu747Asp)
c.2117A>T
c.2208A>T (p.Glu736Asp)
c.2358A>T (p.Glu786Asp)
c.155A>T (n.155A>T)
c.809A>T
n.2426A>T
c.2187A>T (p.Glu729Asp)
c.1422A>T (p.Glu474Asp)
3g.130997619C>ACA354536987ATP2C1c.2257C>A (p.Pro753Thr)
c.2242C>A (p.Pro748Thr)
c.2118C>A
c.2209C>A (p.Pro737Thr)
c.2359C>A (p.Pro787Thr)
c.156C>A (n.156C>A)
c.810C>A
n.2427C>A
c.2188C>A (p.Pro730Thr)
c.1423C>A (p.Pro475Thr)
3g.130997619C=CA1401883567ATP2C1c.2257C= (p.Pro753=)
c.2242C= (p.Pro748=)
c.2118C=
c.2209C= (p.Pro737=)
c.2359C= (p.Pro787=)
c.156C= (n.156C=)
c.810C=
n.2427C=
c.2188C= (p.Pro730=)
c.1423C= (p.Pro475=)
3g.130997619C>GCA354536990ATP2C1c.2257C>G (p.Pro753Ala)
c.2242C>G (p.Pro748Ala)
c.2118C>G
c.2209C>G (p.Pro737Ala)
c.2359C>G (p.Pro787Ala)
c.156C>G (n.156C>G)
c.810C>G
n.2427C>G
c.2188C>G (p.Pro730Ala)
c.1423C>G (p.Pro475Ala)
3g.130997619C>TCA354536992ATP2C1c.2257C>T (p.Pro753Ser)
c.2242C>T (p.Pro748Ser)
c.2118C>T
c.2209C>T (p.Pro737Ser)
c.2359C>T (p.Pro787Ser)
c.156C>T (n.156C>T)
c.810C>T
n.2427C>T
c.2188C>T (p.Pro730Ser)
c.1423C>T (p.Pro475Ser)
dbSNP gnomAD v2 gnomAD v4
3g.130997620C>ACA354537000ATP2C1c.2258C>A (p.Pro753Gln)
c.2243C>A (p.Pro748Gln)
c.2119C>A
c.2210C>A (p.Pro737Gln)
c.2360C>A (p.Pro787Gln)
c.157C>A (n.157C>A)
c.811C>A
n.2428C>A
c.2189C>A (p.Pro730Gln)
c.1424C>A (p.Pro475Gln)
3g.130997620C=CA1401883571ATP2C1c.2258C= (p.Pro753=)
c.2243C= (p.Pro748=)
c.2119C=
c.2210C= (p.Pro737=)
c.2360C= (p.Pro787=)
c.157C= (n.157C=)
c.811C=
n.2428C=
c.2189C= (p.Pro730=)
c.1424C= (p.Pro475=)
3g.130997620C>GCA354536996ATP2C1c.2258C>G (p.Pro753Arg)
c.2243C>G (p.Pro748Arg)
c.2119C>G
c.2210C>G (p.Pro737Arg)
c.2360C>G (p.Pro787Arg)
c.157C>G (n.157C>G)
c.811C>G
n.2428C>G
c.2189C>G (p.Pro730Arg)
c.1424C>G (p.Pro475Arg)
dbSNP gnomAD v3 gnomAD v4
3g.130997620C>TCA354536998ATP2C1c.2258C>T (p.Pro753Leu)
c.2243C>T (p.Pro748Leu)
c.2119C>T
c.2210C>T (p.Pro737Leu)
c.2360C>T (p.Pro787Leu)
c.157C>T (n.157C>T)
c.811C>T
n.2428C>T
c.2189C>T (p.Pro730Leu)
c.1424C>T (p.Pro475Leu)
3g.130997621A=CA1401883574ATP2C1c.2259A= (p.Pro753=)
c.2244A= (p.Pro748=)
c.2120A=
c.2211A= (p.Pro737=)
c.2361A= (p.Pro787=)
c.158A= (n.158A=)
c.812A=
n.2429A=
c.2190A= (p.Pro730=)
c.1425A= (p.Pro475=)
3g.130997621A>CCA435662224ATP2C1c.2259A>C (p.Pro753=)
c.2244A>C (p.Pro748=)
c.2120A>C
c.2211A>C (p.Pro737=)
c.2361A>C (p.Pro787=)
c.158A>C (n.158A>C)
c.812A>C
n.2429A>C
c.2190A>C (p.Pro730=)
c.1425A>C (p.Pro475=)
3g.130997621A>GCA435662225ATP2C1c.2259A>G (p.Pro753=)
c.2244A>G (p.Pro748=)
c.2120A>G
c.2211A>G (p.Pro737=)
c.2361A>G (p.Pro787=)
c.158A>G (n.158A>G)
c.812A>G
n.2429A>G
c.2190A>G (p.Pro730=)
c.1425A>G (p.Pro475=)
dbSNP
3g.130997621A>TCA435662227ATP2C1c.2259A>T (p.Pro753=)
c.2244A>T (p.Pro748=)
c.2120A>T
c.2211A>T (p.Pro737=)
c.2361A>T (p.Pro787=)
c.158A>T (n.158A>T)
c.812A>T
n.2429A>T
c.2190A>T (p.Pro730=)
c.1425A>T (p.Pro475=)
COSMIC COSMIC
3g.130997622G>ACA354537003ATP2C1c.2260G>A (p.Val754Met)
c.2245G>A (p.Val749Met)
c.2121G>A
c.2212G>A (p.Val738Met)
c.2362G>A (p.Val788Met)
c.159G>A (n.159G>A)
c.813G>A
n.2430G>A
c.2191G>A (p.Val731Met)
c.1426G>A (p.Val476Met)
3g.130997622G>CCA354537005ATP2C1c.2260G>C (p.Val754Leu)
c.2245G>C (p.Val749Leu)
c.2121G>C
c.2212G>C (p.Val738Leu)
c.2362G>C (p.Val788Leu)
c.159G>C (n.159G>C)
c.813G>C
n.2430G>C
c.2191G>C (p.Val731Leu)
c.1426G>C (p.Val476Leu)
3g.130997622G>TCA354537008ATP2C1c.2260G>T (p.Val754Leu)
c.2245G>T (p.Val749Leu)
c.2121G>T
c.2212G>T (p.Val738Leu)
c.2362G>T (p.Val788Leu)
c.159G>T (n.159G>T)
c.813G>T
n.2430G>T
c.2191G>T (p.Val731Leu)
c.1426G>T (p.Val476Leu)
gnomAD v4
3g.130997623T>ACA354537011ATP2C1c.2261T>A (p.Val754Glu)
c.2246T>A (p.Val749Glu)
c.2122T>A
c.2213T>A (p.Val738Glu)
c.2363T>A (p.Val788Glu)
c.160T>A (n.160T>A)
c.814T>A
n.2431T>A
c.2192T>A (p.Val731Glu)
c.1427T>A (p.Val476Glu)
gnomAD v4
3g.130997623T>CCA354537013ATP2C1c.2261T>C (p.Val754Ala)
c.2246T>C (p.Val749Ala)
c.2122T>C
c.2213T>C (p.Val738Ala)
c.2363T>C (p.Val788Ala)
c.160T>C (n.160T>C)
c.814T>C
n.2431T>C
c.2192T>C (p.Val731Ala)
c.1427T>C (p.Val476Ala)
3g.130997623T>GCA354537014ATP2C1c.2261T>G (p.Val754Gly)
c.2246T>G (p.Val749Gly)
c.2122T>G
c.2213T>G (p.Val738Gly)
c.2363T>G (p.Val788Gly)
c.160T>G (n.160T>G)
c.814T>G
n.2431T>G
c.2192T>G (p.Val731Gly)
c.1427T>G (p.Val476Gly)
3g.130997624G>ACA435662228ATP2C1c.2262G>A (p.Val754=)
c.2247G>A (p.Val749=)
c.2123G>A
c.2214G>A (p.Val738=)
c.2364G>A (p.Val788=)
c.161G>A (n.161G>A)
c.815G>A
n.2432G>A
c.2193G>A (p.Val731=)
c.1428G>A (p.Val476=)
3g.130997624G>CCA435662230ATP2C1c.2262G>C (p.Val754=)
c.2247G>C (p.Val749=)
c.2123G>C
c.2214G>C (p.Val738=)
c.2364G>C (p.Val788=)
c.161G>C (n.161G>C)
c.815G>C
n.2432G>C
c.2193G>C (p.Val731=)
c.1428G>C (p.Val476=)
gnomAD v4
3g.130997624G>TCA435662233ATP2C1c.2262G>T (p.Val754=)
c.2247G>T (p.Val749=)
c.2123G>T
c.2214G>T (p.Val738=)
c.2364G>T (p.Val788=)
c.161G>T (n.161G>T)
c.815G>T
n.2432G>T
c.2193G>T (p.Val731=)
c.1428G>T (p.Val476=)
3g.130997625G>ACA354537017ATP2C1c.2263G>A (p.Asp755Asn)
c.2248G>A (p.Asp750Asn)
c.2124G>A
c.2215G>A (p.Asp739Asn)
c.2365G>A (p.Asp789Asn)
c.162G>A (n.162G>A)
c.816G>A
n.2433G>A
c.2194G>A (p.Asp732Asn)
c.1429G>A (p.Asp477Asn)
3g.130997625G>CCA354537016ATP2C1c.2263G>C (p.Asp755His)
c.2248G>C (p.Asp750His)
c.2124G>C
c.2215G>C (p.Asp739His)
c.2365G>C (p.Asp789His)
c.162G>C (n.162G>C)
c.816G>C
n.2433G>C
c.2194G>C (p.Asp732His)
c.1429G>C (p.Asp477His)
3g.130997625G>TCA354537015ATP2C1c.2263G>T (p.Asp755Tyr)
c.2248G>T (p.Asp750Tyr)
c.2124G>T
c.2215G>T (p.Asp739Tyr)
c.2365G>T (p.Asp789Tyr)
c.162G>T (n.162G>T)
c.816G>T
n.2433G>T
c.2194G>T (p.Asp732Tyr)
c.1429G>T (p.Asp477Tyr)
3g.130997626delCA2586965907ATP2C1c.2264del (p.Asp755ValfsTer17)
c.2249del (p.Asp750ValfsTer17)
c.2125del
c.2216del (p.Asp739ValfsTer17)
c.2366del (p.Asp789ValfsTer17)
c.163del (n.163del)
c.817del
n.2434del
c.2195del (p.Asp732ValfsTer17)
c.1430del (p.Asp477ValfsTer17)
3g.130997626A>CCA354537019ATP2C1c.2264A>C (p.Asp755Ala)
c.2249A>C (p.Asp750Ala)
c.2125A>C
c.2216A>C (p.Asp739Ala)
c.2366A>C (p.Asp789Ala)
c.163A>C (n.163A>C)
c.817A>C
n.2434A>C
c.2195A>C (p.Asp732Ala)
c.1430A>C (p.Asp477Ala)
3g.130997626A>GCA354537018ATP2C1c.2264A>G (p.Asp755Gly)
c.2249A>G (p.Asp750Gly)
c.2125A>G
c.2216A>G (p.Asp739Gly)
c.2366A>G (p.Asp789Gly)
c.163A>G (n.163A>G)
c.817A>G
n.2434A>G
c.2195A>G (p.Asp732Gly)
c.1430A>G (p.Asp477Gly)
gnomAD v4
3g.130997626A>TCA354537020ATP2C1c.2264A>T (p.Asp755Val)
c.2249A>T (p.Asp750Val)
c.2125A>T
c.2216A>T (p.Asp739Val)
c.2366A>T (p.Asp789Val)
c.163A>T (n.163A>T)
c.817A>T
n.2434A>T
c.2195A>T (p.Asp732Val)
c.1430A>T (p.Asp477Val)
gnomAD v4
3g.130997627T>ACA354537021ATP2C1c.2265T>A (p.Asp755Glu)
c.2250T>A (p.Asp750Glu)
c.2126T>A
c.2217T>A (p.Asp739Glu)
c.2367T>A (p.Asp789Glu)
c.164T>A (n.164T>A)
c.818T>A
n.2435T>A
c.2196T>A (p.Asp732Glu)
c.1431T>A (p.Asp477Glu)
3g.130997627T>CCA435662235ATP2C1c.2265T>C (p.Asp755=)
c.2250T>C (p.Asp750=)
c.2126T>C
c.2217T>C (p.Asp739=)
c.2367T>C (p.Asp789=)
c.164T>C (n.164T>C)
c.818T>C
n.2435T>C
c.2196T>C (p.Asp732=)
c.1431T>C (p.Asp477=)
gnomAD v4
3g.130997627T>GCA354537022ATP2C1c.2265T>G (p.Asp755Glu)
c.2250T>G (p.Asp750Glu)
c.2126T>G
c.2217T>G (p.Asp739Glu)
c.2367T>G (p.Asp789Glu)
c.164T>G (n.164T>G)
c.818T>G
n.2435T>G
c.2196T>G (p.Asp732Glu)
c.1431T>G (p.Asp477Glu)

Number of alleles fetched