Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.41970424G>ACA507694802ATP1A3c.2421C>T (p.Thr807=)
c.2382C>T (p.Thr794=)
c.2415C>T (p.Thr805=)
c.2292C>T (p.Thr764=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
19g.41970424G>CCA507694803ATP1A3c.2421C>G (p.Thr807=)
c.2382C>G (p.Thr794=)
c.2415C>G (p.Thr805=)
c.2292C>G (p.Thr764=)
19g.41970424G=CA2336720943ATP1A3c.2421C= (p.Thr807=)
c.2382C= (p.Thr794=)
c.2415C= (p.Thr805=)
c.2292C= (p.Thr764=)
19g.41970424G>TCA507694804ATP1A3c.2421C>A (p.Thr807=)
c.2382C>A (p.Thr794=)
c.2415C>A (p.Thr805=)
c.2292C>A (p.Thr764=)
 dbSNP
19g.41970425G>ACA406039387ATP1A3c.2420C>T (p.Thr807Ile)
c.2381C>T (p.Thr794Ile)
c.2414C>T (p.Thr805Ile)
c.2291C>T (p.Thr764Ile)
19g.41970425G>CCA406039389ATP1A3c.2420C>G (p.Thr807Ser)
c.2381C>G (p.Thr794Ser)
c.2414C>G (p.Thr805Ser)
c.2291C>G (p.Thr764Ser)
19g.41970425G>TCA406039390ATP1A3c.2420C>A (p.Thr807Asn)
c.2381C>A (p.Thr794Asn)
c.2414C>A (p.Thr805Asn)
c.2291C>A (p.Thr764Asn)
19g.41970426T>ACA406039392ATP1A3c.2419A>T (p.Thr807Ser)
c.2380A>T (p.Thr794Ser)
c.2413A>T (p.Thr805Ser)
c.2290A>T (p.Thr764Ser)
19g.41970426T>CCA406039394ATP1A3c.2419A>G (p.Thr807Ala)
c.2380A>G (p.Thr794Ala)
c.2413A>G (p.Thr805Ala)
c.2290A>G (p.Thr764Ala)
19g.41970426T>GCA406039395ATP1A3c.2419A>C (p.Thr807Pro)
c.2380A>C (p.Thr794Pro)
c.2413A>C (p.Thr805Pro)
c.2290A>C (p.Thr764Pro)
19g.41970427G>ACA507694805ATP1A3c.2418C>T (p.Gly806=)
c.2379C>T (p.Gly793=)
c.2412C>T (p.Gly804=)
c.2289C>T (p.Gly763=)
19g.41970427G>CCA507694806ATP1A3c.2418C>G (p.Gly806=)
c.2379C>G (p.Gly793=)
c.2412C>G (p.Gly804=)
c.2289C>G (p.Gly763=)
19g.41970427G>TCA507694807ATP1A3c.2418C>A (p.Gly806=)
c.2379C>A (p.Gly793=)
c.2412C>A (p.Gly804=)
c.2289C>A (p.Gly763=)
19g.41970428C>ACA406039399ATP1A3c.2417G>T (p.Gly806Val)
c.2378G>T (p.Gly793Val)
c.2411G>T (p.Gly804Val)
c.2288G>T (p.Gly763Val)
19g.41970428C>GCA406039398ATP1A3c.2417G>C (p.Gly806Ala)
c.2378G>C (p.Gly793Ala)
c.2411G>C (p.Gly804Ala)
c.2288G>C (p.Gly763Ala)
19g.41970428C>TCA406039396ATP1A3c.2417G>A (p.Gly806Asp)
c.2378G>A (p.Gly793Asp)
c.2411G>A (p.Gly804Asp)
c.2288G>A (p.Gly763Asp)
19g.41970429C>ACA406039400ATP1A3c.2416G>T (p.Gly806Cys)
c.2377G>T (p.Gly793Cys)
c.2410G>T (p.Gly804Cys)
c.2287G>T (p.Gly763Cys)
 COSMIC
19g.41970429C>GCA406039401ATP1A3c.2416G>C (p.Gly806Arg)
c.2377G>C (p.Gly793Arg)
c.2410G>C (p.Gly804Arg)
c.2287G>C (p.Gly763Arg)
19g.41970429C>TCA406039402ATP1A3c.2416G>A (p.Gly806Ser)
c.2377G>A (p.Gly793Ser)
c.2410G>A (p.Gly804Ser)
c.2287G>A (p.Gly763Ser)
 gnomAD v4
19g.41970430C>ACA507694808ATP1A3c.2415G>T (p.Leu805=)
c.2376G>T (p.Leu792=)
c.2409G>T (p.Leu803=)
c.2286G>T (p.Leu762=)
19g.41970430C=CA2336720945ATP1A3c.2415G= (p.Leu805=)
c.2376G= (p.Leu792=)
c.2409G= (p.Leu803=)
c.2286G= (p.Leu762=)
19g.41970430C>GCA507694809ATP1A3c.2415G>C (p.Leu805=)
c.2376G>C (p.Leu792=)
c.2409G>C (p.Leu803=)
c.2286G>C (p.Leu762=)
19g.41970430C>TCA507694810ATP1A3c.2415G>A (p.Leu805=)
c.2376G>A (p.Leu792=)
c.2409G>A (p.Leu803=)
c.2286G>A (p.Leu762=)
 dbSNP gnomAD v2 gnomAD v4
19g.41970430_41970431delinsCACA2336720946ATP1A3c.2414_2415delinsTG (p.Leu805=)
c.2375_2376delinsTG (p.Leu792=)
c.2408_2409delinsTG (p.Leu803=)
c.2285_2286delinsTG (p.Leu762=)
19g.41970431delCA2336720948ATP1A3c.2414del (p.Leu805ArgfsTer?)
c.2375del (p.Leu792ArgfsTer?)
c.2408del (p.Leu803ArgfsTer?)
c.2285del (p.Leu762ArgfsTer?)
 dbSNP gnomAD v4
19g.41970431A=CA2336720949ATP1A3c.2414T= (p.Leu805=)
c.2375T= (p.Leu792=)
c.2408T= (p.Leu803=)
c.2285T= (p.Leu762=)
19g.41970431A>CCA406039403ATP1A3c.2414T>G (p.Leu805Arg)
c.2375T>G (p.Leu792Arg)
c.2408T>G (p.Leu803Arg)
c.2285T>G (p.Leu762Arg)
19g.41970431A>GCA406039404ATP1A3c.2414T>C (p.Leu805Pro)
c.2375T>C (p.Leu792Pro)
c.2408T>C (p.Leu803Pro)
c.2285T>C (p.Leu762Pro)
19g.41970431A>TCA406039405ATP1A3c.2414T>A (p.Leu805Gln)
c.2375T>A (p.Leu792Gln)
c.2408T>A (p.Leu803Gln)
c.2285T>A (p.Leu762Gln)
19g.41970432G>ACA507694811ATP1A3c.2413C>T (p.Leu805=)
c.2374C>T (p.Leu792=)
c.2407C>T (p.Leu803=)
c.2284C>T (p.Leu762=)
 gnomAD v4
19g.41970432G>CCA406039407ATP1A3c.2413C>G (p.Leu805Val)
c.2374C>G (p.Leu792Val)
c.2407C>G (p.Leu803Val)
c.2284C>G (p.Leu762Val)
19g.41970432G>TCA406039406ATP1A3c.2413C>A (p.Leu805Met)
c.2374C>A (p.Leu792Met)
c.2407C>A (p.Leu803Met)
c.2284C>A (p.Leu762Met)
19g.41970435dupCA2336720951ATP1A3c.2413dup (p.Leu805ProfsTer14)
c.2374dup (p.Leu792ProfsTer14)
c.2407dup (p.Leu803ProfsTer14)
c.2284dup (p.Leu762ProfsTer14)
 dbSNP
19g.41970433G>ACA507694812ATP1A3c.2412C>T (p.Pro804=)
c.2373C>T (p.Pro791=)
c.2406C>T (p.Pro802=)
c.2283C>T (p.Pro761=)
 gnomAD v4
19g.41970433G>CCA507694813ATP1A3c.2412C>G (p.Pro804=)
c.2373C>G (p.Pro791=)
c.2406C>G (p.Pro802=)
c.2283C>G (p.Pro761=)
19g.41970433G>TCA507694814ATP1A3c.2412C>A (p.Pro804=)
c.2373C>A (p.Pro791=)
c.2406C>A (p.Pro802=)
c.2283C>A (p.Pro761=)
19g.41970434G>ACA406039408ATP1A3c.2411C>T (p.Pro804Leu)
c.2372C>T (p.Pro791Leu)
c.2405C>T (p.Pro802Leu)
c.2282C>T (p.Pro761Leu)
19g.41970434G>CCA406039409ATP1A3c.2411C>G (p.Pro804Arg)
c.2372C>G (p.Pro791Arg)
c.2405C>G (p.Pro802Arg)
c.2282C>G (p.Pro761Arg)
19g.41970434G>TCA406039410ATP1A3c.2411C>A (p.Pro804His)
c.2372C>A (p.Pro791His)
c.2405C>A (p.Pro802His)
c.2282C>A (p.Pro761His)
19g.41970435G>ACA406039411ATP1A3c.2410C>T (p.Pro804Ser)
c.2371C>T (p.Pro791Ser)
c.2404C>T (p.Pro802Ser)
c.2281C>T (p.Pro761Ser)
 ClinVar dbSNP gnomAD v4
19g.41970435G>CCA406039412ATP1A3c.2410C>G (p.Pro804Ala)
c.2371C>G (p.Pro791Ala)
c.2404C>G (p.Pro802Ala)
c.2281C>G (p.Pro761Ala)
19g.41970435G=CA2336720953ATP1A3c.2410C= (p.Pro804=)
c.2371C= (p.Pro791=)
c.2404C= (p.Pro802=)
c.2281C= (p.Pro761=)
19g.41970435G>TCA406039413ATP1A3c.2410C>A (p.Pro804Thr)
c.2371C>A (p.Pro791Thr)
c.2404C>A (p.Pro802Thr)
c.2281C>A (p.Pro761Thr)
19g.41970436C>ACA507694815ATP1A3c.2409G>T (p.Leu803=)
c.2370G>T (p.Leu790=)
c.2403G>T (p.Leu801=)
c.2280G>T (p.Leu760=)
19g.41970436C=CA2336720955ATP1A3c.2409G= (p.Leu803=)
c.2370G= (p.Leu790=)
c.2403G= (p.Leu801=)
c.2280G= (p.Leu760=)
19g.41970436C>GCA507694816ATP1A3c.2409G>C (p.Leu803=)
c.2370G>C (p.Leu790=)
c.2403G>C (p.Leu801=)
c.2280G>C (p.Leu760=)
19g.41970436C>TCA507694817ATP1A3c.2409G>A (p.Leu803=)
c.2370G>A (p.Leu790=)
c.2403G>A (p.Leu801=)
c.2280G>A (p.Leu760=)
 dbSNP
19g.41970437A>CCA406039416ATP1A3c.2408T>G (p.Leu803Arg)
c.2369T>G (p.Leu790Arg)
c.2402T>G (p.Leu801Arg)
c.2279T>G (p.Leu760Arg)
19g.41970437A>GCA406039414ATP1A3c.2408T>C (p.Leu803Pro)
c.2369T>C (p.Leu790Pro)
c.2402T>C (p.Leu801Pro)
c.2279T>C (p.Leu760Pro)
19g.41970437A>TCA406039415ATP1A3c.2408T>A (p.Leu803Gln)
c.2369T>A (p.Leu790Gln)
c.2402T>A (p.Leu801Gln)
c.2279T>A (p.Leu760Gln)
19g.41970438G>ACA507694818ATP1A3c.2407C>T (p.Leu803=)
c.2368C>T (p.Leu790=)
c.2401C>T (p.Leu801=)
c.2278C>T (p.Leu760=)
 gnomAD v4
19g.41970438G>CCA406039417ATP1A3c.2407C>G (p.Leu803Val)
c.2368C>G (p.Leu790Val)
c.2401C>G (p.Leu801Val)
c.2278C>G (p.Leu760Val)
19g.41970438G>TCA406039418ATP1A3c.2407C>A (p.Leu803Met)
c.2368C>A (p.Leu790Met)
c.2401C>A (p.Leu801Met)
c.2278C>A (p.Leu760Met)
19g.41970439C>ACA507694819ATP1A3c.2406G>T (p.Pro802=)
c.2367G>T (p.Pro789=)
c.2400G>T (p.Pro800=)
c.2277G>T (p.Pro759=)
 gnomAD v4
19g.41970439C=CA2336720957ATP1A3c.2406G= (p.Pro802=)
c.2367G= (p.Pro789=)
c.2400G= (p.Pro800=)
c.2277G= (p.Pro759=)
19g.41970439C>GCA507694820ATP1A3c.2406G>C (p.Pro802=)
c.2367G>C (p.Pro789=)
c.2400G>C (p.Pro800=)
c.2277G>C (p.Pro759=)
19g.41970439C>TCA9467411ATP1A3c.2406G>A (p.Pro802=)
c.2367G>A (p.Pro789=)
c.2400G>A (p.Pro800=)
c.2277G>A (p.Pro759=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.41970440G>ACA406039421ATP1A3c.2405C>T (p.Pro802Leu)
c.2366C>T (p.Pro789Leu)
c.2399C>T (p.Pro800Leu)
c.2276C>T (p.Pro759Leu)
 ClinVar dbSNP gnomAD v4
19g.41970440G>CCA406039422ATP1A3c.2405C>G (p.Pro802Arg)
c.2366C>G (p.Pro789Arg)
c.2399C>G (p.Pro800Arg)
c.2276C>G (p.Pro759Arg)
19g.41970440G>TCA406039423ATP1A3c.2405C>A (p.Pro802Gln)
c.2366C>A (p.Pro789Gln)
c.2399C>A (p.Pro800Gln)
c.2276C>A (p.Pro759Gln)
19g.41970441G>ACA406039425ATP1A3c.2404C>T (p.Pro802Ser)
c.2365C>T (p.Pro789Ser)
c.2398C>T (p.Pro800Ser)
c.2275C>T (p.Pro759Ser)
19g.41970441G>CCA406039426ATP1A3c.2404C>G (p.Pro802Ala)
c.2365C>G (p.Pro789Ala)
c.2398C>G (p.Pro800Ala)
c.2275C>G (p.Pro759Ala)
 gnomAD v4
19g.41970441G>TCA406039428ATP1A3c.2404C>A (p.Pro802Thr)
c.2365C>A (p.Pro789Thr)
c.2398C>A (p.Pro800Thr)
c.2275C>A (p.Pro759Thr)
19g.41970442G>ACA507694821ATP1A3c.2403C>T (p.Ile801=)
c.2364C>T (p.Ile788=)
c.2397C>T (p.Ile799=)
c.2274C>T (p.Ile758=)
 ClinVar dbSNP
19g.41970442G>CCA406039430ATP1A3c.2403C>G (p.Ile801Met)
c.2364C>G (p.Ile788Met)
c.2397C>G (p.Ile799Met)
c.2274C>G (p.Ile758Met)
 dbSNP gnomAD v2 gnomAD v4
19g.41970442G=CA2336720961ATP1A3c.2403C= (p.Ile801=)
c.2364C= (p.Ile788=)
c.2397C= (p.Ile799=)
c.2274C= (p.Ile758=)
19g.41970442G>TCA507694822ATP1A3c.2403C>A (p.Ile801=)
c.2364C>A (p.Ile788=)
c.2397C>A (p.Ile799=)
c.2274C>A (p.Ile758=)
 ClinVar gnomAD v4
19g.41970443A>CCA406039432ATP1A3c.2402T>G (p.Ile801Ser)
c.2363T>G (p.Ile788Ser)
c.2396T>G (p.Ile799Ser)
c.2273T>G (p.Ile758Ser)
19g.41970443A>GCA406039434ATP1A3c.2402T>C (p.Ile801Thr)
c.2363T>C (p.Ile788Thr)
c.2396T>C (p.Ile799Thr)
c.2273T>C (p.Ile758Thr)
19g.41970443A>TCA406039436ATP1A3c.2402T>A (p.Ile801Asn)
c.2363T>A (p.Ile788Asn)
c.2396T>A (p.Ile799Asn)
c.2273T>A (p.Ile758Asn)
19g.41970444T>ACA406039438ATP1A3c.2401A>T (p.Ile801Phe)
c.2362A>T (p.Ile788Phe)
c.2395A>T (p.Ile799Phe)
c.2272A>T (p.Ile758Phe)
19g.41970444T>CCA406039442ATP1A3c.2401A>G (p.Ile801Val)
c.2362A>G (p.Ile788Val)
c.2395A>G (p.Ile799Val)
c.2272A>G (p.Ile758Val)
19g.41970444T>GCA406039439ATP1A3c.2401A>C (p.Ile801Leu)
c.2362A>C (p.Ile788Leu)
c.2395A>C (p.Ile799Leu)
c.2272A>C (p.Ile758Leu)
19g.41970445G>ACA507694823ATP1A3c.2400C>T (p.Asn800=)
c.2361C>T (p.Asn787=)
c.2394C>T (p.Asn798=)
c.2271C>T (p.Asn757=)
 gnomAD v4
19g.41970445G>CCA406039443ATP1A3c.2400C>G (p.Asn800Lys)
c.2361C>G (p.Asn787Lys)
c.2394C>G (p.Asn798Lys)
c.2271C>G (p.Asn757Lys)
19g.41970445G>TCA406039445ATP1A3c.2400C>A (p.Asn800Lys)
c.2361C>A (p.Asn787Lys)
c.2394C>A (p.Asn798Lys)
c.2271C>A (p.Asn757Lys)
19g.41970446T>ACA406039447ATP1A3c.2399A>T (p.Asn800Ile)
c.2360A>T (p.Asn787Ile)
c.2393A>T (p.Asn798Ile)
c.2270A>T (p.Asn757Ile)
19g.41970446T>CCA406039448ATP1A3c.2399A>G (p.Asn800Ser)
c.2360A>G (p.Asn787Ser)
c.2393A>G (p.Asn798Ser)
c.2270A>G (p.Asn757Ser)
 COSMIC
19g.41970446T>GCA406039450ATP1A3c.2399A>C (p.Asn800Thr)
c.2360A>C (p.Asn787Thr)
c.2393A>C (p.Asn798Thr)
c.2270A>C (p.Asn757Thr)
19g.41970447T>ACA406039456ATP1A3c.2398A>T (p.Asn800Tyr)
c.2359A>T (p.Asn787Tyr)
c.2392A>T (p.Asn798Tyr)
c.2269A>T (p.Asn757Tyr)
19g.41970447T>CCA406039454ATP1A3c.2398A>G (p.Asn800Asp)
c.2359A>G (p.Asn787Asp)
c.2392A>G (p.Asn798Asp)
c.2269A>G (p.Asn757Asp)
19g.41970447T>GCA406039452ATP1A3c.2398A>C (p.Asn800His)
c.2359A>C (p.Asn787His)
c.2392A>C (p.Asn798His)
c.2269A>C (p.Asn757His)
19g.41970448G>ACA507694824ATP1A3c.2397C>T (p.Ala799=)
c.2358C>T (p.Ala786=)
c.2391C>T (p.Ala797=)
c.2268C>T (p.Ala756=)
 gnomAD v4
19g.41970448G>CCA507694825ATP1A3c.2397C>G (p.Ala799=)
c.2358C>G (p.Ala786=)
c.2391C>G (p.Ala797=)
c.2268C>G (p.Ala756=)
19g.41970448G>TCA507694826ATP1A3c.2397C>A (p.Ala799=)
c.2358C>A (p.Ala786=)
c.2391C>A (p.Ala797=)
c.2268C>A (p.Ala756=)
19g.41970449G>ACA406039458ATP1A3c.2396C>T (p.Ala799Val)
c.2357C>T (p.Ala786Val)
c.2390C>T (p.Ala797Val)
c.2267C>T (p.Ala756Val)
19g.41970449G>CCA406039459ATP1A3c.2396C>G (p.Ala799Gly)
c.2357C>G (p.Ala786Gly)
c.2390C>G (p.Ala797Gly)
c.2267C>G (p.Ala756Gly)
19g.41970449G>TCA406039461ATP1A3c.2396C>A (p.Ala799Asp)
c.2357C>A (p.Ala786Asp)
c.2390C>A (p.Ala797Asp)
c.2267C>A (p.Ala756Asp)
19g.41970450C>ACA406039463ATP1A3c.2395G>T (p.Ala799Ser)
c.2356G>T (p.Ala786Ser)
c.2389G>T (p.Ala797Ser)
c.2266G>T (p.Ala756Ser)
 gnomAD v4
19g.41970450C>GCA406039465ATP1A3c.2395G>C (p.Ala799Pro)
c.2356G>C (p.Ala786Pro)
c.2389G>C (p.Ala797Pro)
c.2266G>C (p.Ala756Pro)
19g.41970450C>TCA406039466ATP1A3c.2395G>A (p.Ala799Thr)
c.2356G>A (p.Ala786Thr)
c.2389G>A (p.Ala797Thr)
c.2266G>A (p.Ala756Thr)
19g.41970451C>ACA406039467ATP1A3c.2394G>T (p.Met798Ile)
c.2355G>T (p.Met785Ile)
c.2388G>T (p.Met796Ile)
c.2265G>T (p.Met755Ile)
19g.41970451C>GCA406039469ATP1A3c.2394G>C (p.Met798Ile)
c.2355G>C (p.Met785Ile)
c.2388G>C (p.Met796Ile)
c.2265G>C (p.Met755Ile)
19g.41970451C>TCA406039468ATP1A3c.2394G>A (p.Met798Ile)
c.2355G>A (p.Met785Ile)
c.2388G>A (p.Met796Ile)
c.2265G>A (p.Met755Ile)
19g.41970452A=CA2336720962ATP1A3c.2393T= (p.Met798=)
c.2354T= (p.Met785=)
c.2387T= (p.Met796=)
c.2264T= (p.Met755=)
19g.41970452A>CCA406039470ATP1A3c.2393T>G (p.Met798Arg)
c.2354T>G (p.Met785Arg)
c.2387T>G (p.Met796Arg)
c.2264T>G (p.Met755Arg)
19g.41970452A>GCA406039471ATP1A3c.2393T>C (p.Met798Thr)
c.2354T>C (p.Met785Thr)
c.2387T>C (p.Met796Thr)
c.2264T>C (p.Met755Thr)
19g.41970452A>TCA406039472ATP1A3c.2393T>A (p.Met798Lys)
c.2354T>A (p.Met785Lys)
c.2387T>A (p.Met796Lys)
c.2264T>A (p.Met755Lys)
 ClinVar dbSNP
19g.41970453T>ACA406039474ATP1A3c.2392A>T (p.Met798Leu)
c.2353A>T (p.Met785Leu)
c.2386A>T (p.Met796Leu)
c.2263A>T (p.Met755Leu)
19g.41970453T>CCA406039475ATP1A3c.2392A>G (p.Met798Val)
c.2353A>G (p.Met785Val)
c.2386A>G (p.Met796Val)
c.2263A>G (p.Met755Val)
 ClinVar
19g.41970453T>GCA406039477ATP1A3c.2392A>C (p.Met798Leu)
c.2353A>C (p.Met785Leu)
c.2386A>C (p.Met796Leu)
c.2263A>C (p.Met755Leu)
 gnomAD v4
19g.41970454G>ACA507694827ATP1A3c.2391C>T (p.Ile797=)
c.2352C>T (p.Ile784=)
c.2385C>T (p.Ile795=)
c.2262C>T (p.Ile754=)
19g.41970454G>CCA406039479ATP1A3c.2391C>G (p.Ile797Met)
c.2352C>G (p.Ile784Met)
c.2385C>G (p.Ile795Met)
c.2262C>G (p.Ile754Met)
19g.41970454G>TCA507694828ATP1A3c.2391C>A (p.Ile797=)
c.2352C>A (p.Ile784=)
c.2385C>A (p.Ile795=)
c.2262C>A (p.Ile754=)
19g.41970455A>CCA406039480ATP1A3c.2390T>G (p.Ile797Ser)
c.2351T>G (p.Ile784Ser)
c.2384T>G (p.Ile795Ser)
c.2261T>G (p.Ile754Ser)
19g.41970455A>GCA406039481ATP1A3c.2390T>C (p.Ile797Thr)
c.2351T>C (p.Ile784Thr)
c.2384T>C (p.Ile795Thr)
c.2261T>C (p.Ile754Thr)
19g.41970455A>TCA406039483ATP1A3c.2390T>A (p.Ile797Asn)
c.2351T>A (p.Ile784Asn)
c.2384T>A (p.Ile795Asn)
c.2261T>A (p.Ile754Asn)
19g.41970456T>ACA406039488ATP1A3c.2389A>T (p.Ile797Phe)
c.2350A>T (p.Ile784Phe)
c.2383A>T (p.Ile795Phe)
c.2260A>T (p.Ile754Phe)
19g.41970456T>CCA406039487ATP1A3c.2389A>G (p.Ile797Val)
c.2350A>G (p.Ile784Val)
c.2383A>G (p.Ile795Val)
c.2260A>G (p.Ile754Val)
19g.41970456T>GCA406039486ATP1A3c.2389A>C (p.Ile797Leu)
c.2350A>C (p.Ile784Leu)
c.2383A>C (p.Ile795Leu)
c.2260A>C (p.Ile754Leu)
19g.41970457G>ACA507694829ATP1A3c.2388C>T (p.Phe796=)
c.2349C>T (p.Phe783=)
c.2382C>T (p.Phe794=)
c.2259C>T (p.Phe753=)
19g.41970457G>CCA406039490ATP1A3c.2388C>G (p.Phe796Leu)
c.2349C>G (p.Phe783Leu)
c.2382C>G (p.Phe794Leu)
c.2259C>G (p.Phe753Leu)
19g.41970457G>TCA406039492ATP1A3c.2388C>A (p.Phe796Leu)
c.2349C>A (p.Phe783Leu)
c.2382C>A (p.Phe794Leu)
c.2259C>A (p.Phe753Leu)
 COSMIC
19g.41970458A>CCA406039494ATP1A3c.2387T>G (p.Phe796Cys)
c.2348T>G (p.Phe783Cys)
c.2381T>G (p.Phe794Cys)
c.2258T>G (p.Phe753Cys)
19g.41970458A>GCA406039496ATP1A3c.2387T>C (p.Phe796Ser)
c.2348T>C (p.Phe783Ser)
c.2381T>C (p.Phe794Ser)
c.2258T>C (p.Phe753Ser)
19g.41970458A>TCA406039495ATP1A3c.2387T>A (p.Phe796Tyr)
c.2348T>A (p.Phe783Tyr)
c.2381T>A (p.Phe794Tyr)
c.2258T>A (p.Phe753Tyr)
19g.41970459A>CCA406039498ATP1A3c.2386T>G (p.Phe796Val)
c.2347T>G (p.Phe783Val)
c.2380T>G (p.Phe794Val)
c.2257T>G (p.Phe753Val)
19g.41970459A>GCA406039500ATP1A3c.2386T>C (p.Phe796Leu)
c.2347T>C (p.Phe783Leu)
c.2380T>C (p.Phe794Leu)
c.2257T>C (p.Phe753Leu)
19g.41970459A>TCA406039502ATP1A3c.2386T>A (p.Phe796Ile)
c.2347T>A (p.Phe783Ile)
c.2380T>A (p.Phe794Ile)
c.2257T>A (p.Phe753Ile)
19g.41970460C>ACA507694830ATP1A3c.2385G>T (p.Leu795=)
c.2346G>T (p.Leu782=)
c.2379G>T (p.Leu793=)
c.2256G>T (p.Leu752=)
19g.41970460C=CA2336720964ATP1A3c.2385G= (p.Leu795=)
c.2346G= (p.Leu782=)
c.2379G= (p.Leu793=)
c.2256G= (p.Leu752=)
19g.41970460C>GCA507694831ATP1A3c.2385G>C (p.Leu795=)
c.2346G>C (p.Leu782=)
c.2379G>C (p.Leu793=)
c.2256G>C (p.Leu752=)
 gnomAD v4
19g.41970460C>TCA507694832ATP1A3c.2385G>A (p.Leu795=)
c.2346G>A (p.Leu782=)
c.2379G>A (p.Leu793=)
c.2256G>A (p.Leu752=)
 dbSNP
19g.41970461A>CCA406039503ATP1A3c.2384T>G (p.Leu795Arg)
c.2345T>G (p.Leu782Arg)
c.2378T>G (p.Leu793Arg)
c.2255T>G (p.Leu752Arg)
19g.41970461A>GCA406039504ATP1A3c.2384T>C (p.Leu795Pro)
c.2345T>C (p.Leu782Pro)
c.2378T>C (p.Leu793Pro)
c.2255T>C (p.Leu752Pro)
19g.41970461A>TCA406039506ATP1A3c.2384T>A (p.Leu795Gln)
c.2345T>A (p.Leu782Gln)
c.2378T>A (p.Leu793Gln)
c.2255T>A (p.Leu752Gln)
19g.41970462G>ACA507694833ATP1A3c.2383C>T (p.Leu795=)
c.2344C>T (p.Leu782=)
c.2377C>T (p.Leu793=)
c.2254C>T (p.Leu752=)
19g.41970462G>CCA406039508ATP1A3c.2383C>G (p.Leu795Val)
c.2344C>G (p.Leu782Val)
c.2377C>G (p.Leu793Val)
c.2254C>G (p.Leu752Val)
19g.41970462G>TCA406039510ATP1A3c.2383C>A (p.Leu795Met)
c.2344C>A (p.Leu782Met)
c.2377C>A (p.Leu793Met)
c.2254C>A (p.Leu752Met)
19g.41970463C>ACA507694835ATP1A3c.2382G>T (p.Leu794=)
c.2343G>T (p.Leu781=)
c.2376G>T (p.Leu792=)
c.2253G>T (p.Leu751=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41970463C=CA2336720966ATP1A3c.2382G= (p.Leu794=)
c.2343G= (p.Leu781=)
c.2376G= (p.Leu792=)
c.2253G= (p.Leu751=)
19g.41970463C>GCA507694836ATP1A3c.2382G>C (p.Leu794=)
c.2343G>C (p.Leu781=)
c.2376G>C (p.Leu792=)
c.2253G>C (p.Leu751=)
19g.41970463C>TCA507694834ATP1A3c.2382G>A (p.Leu794=)
c.2343G>A (p.Leu781=)
c.2376G>A (p.Leu792=)
c.2253G>A (p.Leu751=)
 gnomAD v4
19g.41970464A>CCA406039512ATP1A3c.2381T>G (p.Leu794Arg)
c.2342T>G (p.Leu781Arg)
c.2375T>G (p.Leu792Arg)
c.2252T>G (p.Leu751Arg)
19g.41970464A>GCA406039515ATP1A3c.2381T>C (p.Leu794Pro)
c.2342T>C (p.Leu781Pro)
c.2375T>C (p.Leu792Pro)
c.2252T>C (p.Leu751Pro)
19g.41970464A>TCA406039513ATP1A3c.2381T>A (p.Leu794Gln)
c.2342T>A (p.Leu781Gln)
c.2375T>A (p.Leu792Gln)
c.2252T>A (p.Leu751Gln)
19g.41970465G>ACA507694837ATP1A3c.2380C>T (p.Leu794=)
c.2341C>T (p.Leu781=)
c.2374C>T (p.Leu792=)
c.2251C>T (p.Leu751=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41970465G>CCA406039517ATP1A3c.2380C>G (p.Leu794Val)
c.2341C>G (p.Leu781Val)
c.2374C>G (p.Leu792Val)
c.2251C>G (p.Leu751Val)
19g.41970465G=CA2336720968ATP1A3c.2380C= (p.Leu794=)
c.2341C= (p.Leu781=)
c.2374C= (p.Leu792=)
c.2251C= (p.Leu751=)
19g.41970465G>TCA406039518ATP1A3c.2380C>A (p.Leu794Met)
c.2341C>A (p.Leu781Met)
c.2374C>A (p.Leu792Met)
c.2251C>A (p.Leu751Met)
19g.41970466G>ACA507694838ATP1A3c.2379C>T (p.Phe793=)
c.2340C>T (p.Phe780=)
c.2373C>T (p.Phe791=)
c.2250C>T (p.Phe750=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
19g.41970466G>CCA406039520ATP1A3c.2379C>G (p.Phe793Leu)
c.2340C>G (p.Phe780Leu)
c.2373C>G (p.Phe791Leu)
c.2250C>G (p.Phe750Leu)
19g.41970466G=CA2336720969ATP1A3c.2379C= (p.Phe793=)
c.2340C= (p.Phe780=)
c.2373C= (p.Phe791=)
c.2250C= (p.Phe750=)
19g.41970466G>TCA406039522ATP1A3c.2379C>A (p.Phe793Leu)
c.2340C>A (p.Phe780Leu)
c.2373C>A (p.Phe791Leu)
c.2250C>A (p.Phe750Leu)
19g.41970467A>CCA406039527ATP1A3c.2378T>G (p.Phe793Cys)
c.2339T>G (p.Phe780Cys)
c.2372T>G (p.Phe791Cys)
c.2249T>G (p.Phe750Cys)
19g.41970467A>GCA406039524ATP1A3c.2378T>C (p.Phe793Ser)
c.2339T>C (p.Phe780Ser)
c.2372T>C (p.Phe791Ser)
c.2249T>C (p.Phe750Ser)
19g.41970467A>TCA406039525ATP1A3c.2378T>A (p.Phe793Tyr)
c.2339T>A (p.Phe780Tyr)
c.2372T>A (p.Phe791Tyr)
c.2249T>A (p.Phe750Tyr)
19g.41970468A=CA2336720971ATP1A3c.2377T= (p.Phe793=)
c.2338T= (p.Phe780=)
c.2371T= (p.Phe791=)
c.2248T= (p.Phe750=)
19g.41970468A>CCA406039529ATP1A3c.2377T>G (p.Phe793Val)
c.2338T>G (p.Phe780Val)
c.2371T>G (p.Phe791Val)
c.2248T>G (p.Phe750Val)
19g.41970468A>GCA341237ATP1A3c.2377T>C (p.Phe793Leu)
c.2338T>C (p.Phe780Leu)
c.2371T>C (p.Phe791Leu)
c.2248T>C (p.Phe750Leu)
 ClinVar dbSNP
19g.41970468A>TCA406039531ATP1A3c.2377T>A (p.Phe793Ile)
c.2338T>A (p.Phe780Ile)
c.2371T>A (p.Phe791Ile)
c.2248T>A (p.Phe750Ile)
19g.41970469G>ACA507694839ATP1A3c.2376C>T (p.Pro792=)
c.2337C>T (p.Pro779=)
c.2370C>T (p.Pro790=)
c.2247C>T (p.Pro749=)
 dbSNP
19g.41970469G>CCA507694840ATP1A3c.2376C>G (p.Pro792=)
c.2337C>G (p.Pro779=)
c.2370C>G (p.Pro790=)
c.2247C>G (p.Pro749=)
19g.41970469G=CA2336720976ATP1A3c.2376C= (p.Pro792=)
c.2337C= (p.Pro779=)
c.2370C= (p.Pro790=)
c.2247C= (p.Pro749=)
19g.41970469G>TCA507694841ATP1A3c.2376C>A (p.Pro792=)
c.2337C>A (p.Pro779=)
c.2370C>A (p.Pro790=)
c.2247C>A (p.Pro749=)
19g.41970470G>ACA406039533ATP1A3c.2375C>T (p.Pro792Leu)
c.2336C>T (p.Pro779Leu)
c.2369C>T (p.Pro790Leu)
c.2246C>T (p.Pro749Leu)
19g.41970470G>CCA406039535ATP1A3c.2375C>G (p.Pro792Arg)
c.2336C>G (p.Pro779Arg)
c.2369C>G (p.Pro790Arg)
c.2246C>G (p.Pro749Arg)
19g.41970470G>TCA406039536ATP1A3c.2375C>A (p.Pro792His)
c.2336C>A (p.Pro779His)
c.2369C>A (p.Pro790His)
c.2246C>A (p.Pro749His)
19g.41970471G>ACA406039538ATP1A3c.2374C>T (p.Pro792Ser)
c.2335C>T (p.Pro779Ser)
c.2368C>T (p.Pro790Ser)
c.2245C>T (p.Pro749Ser)
19g.41970471G>CCA406039540ATP1A3c.2374C>G (p.Pro792Ala)
c.2335C>G (p.Pro779Ala)
c.2368C>G (p.Pro790Ala)
c.2245C>G (p.Pro749Ala)
19g.41970471G>TCA406039542ATP1A3c.2374C>A (p.Pro792Thr)
c.2335C>A (p.Pro779Thr)
c.2368C>A (p.Pro790Thr)
c.2245C>A (p.Pro749Thr)
19g.41970472C>ACA507694842ATP1A3c.2373G>T (p.Thr791=)
c.2334G>T (p.Thr778=)
c.2367G>T (p.Thr789=)
c.2244G>T (p.Thr748=)
 dbSNP
19g.41970472C=CA2336720980ATP1A3c.2373G= (p.Thr791=)
c.2334G= (p.Thr778=)
c.2367G= (p.Thr789=)
c.2244G= (p.Thr748=)
19g.41970472C>GCA507694843ATP1A3c.2373G>C (p.Thr791=)
c.2334G>C (p.Thr778=)
c.2367G>C (p.Thr789=)
c.2244G>C (p.Thr748=)
19g.41970472C>TCA9467412ATP1A3c.2373G>A (p.Thr791=)
c.2334G>A (p.Thr778=)
c.2367G>A (p.Thr789=)
c.2244G>A (p.Thr748=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41970473G>ACA406039545ATP1A3c.2372C>T (p.Thr791Met)
c.2333C>T (p.Thr778Met)
c.2366C>T (p.Thr789Met)
c.2243C>T (p.Thr748Met)
 gnomAD v4
19g.41970473G>CCA406039546ATP1A3c.2372C>G (p.Thr791Arg)
c.2333C>G (p.Thr778Arg)
c.2366C>G (p.Thr789Arg)
c.2243C>G (p.Thr748Arg)
19g.41970473G>TCA406039548ATP1A3c.2372C>A (p.Thr791Lys)
c.2333C>A (p.Thr778Lys)
c.2366C>A (p.Thr789Lys)
c.2243C>A (p.Thr748Lys)
19g.41970474T>ACA406039549ATP1A3c.2371A>T (p.Thr791Ser)
c.2332A>T (p.Thr778Ser)
c.2365A>T (p.Thr789Ser)
c.2242A>T (p.Thr748Ser)
19g.41970474T>CCA406039553ATP1A3c.2371A>G (p.Thr791Ala)
c.2332A>G (p.Thr778Ala)
c.2365A>G (p.Thr789Ala)
c.2242A>G (p.Thr748Ala)
19g.41970474T>GCA406039551ATP1A3c.2371A>C (p.Thr791Pro)
c.2332A>C (p.Thr778Pro)
c.2365A>C (p.Thr789Pro)
c.2242A>C (p.Thr748Pro)
 ClinVar dbSNP
19g.41970474T=CA2336720987ATP1A3c.2371A= (p.Thr791=)
c.2332A= (p.Thr778=)
c.2365A= (p.Thr789=)
c.2242A= (p.Thr748=)
19g.41970475G>ACA9467413ATP1A3c.2370C>T (p.Ile790=)
c.2331C>T (p.Ile777=)
c.2364C>T (p.Ile788=)
c.2241C>T (p.Ile747=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.41970475G>CCA406039555ATP1A3c.2370C>G (p.Ile790Met)
c.2331C>G (p.Ile777Met)
c.2364C>G (p.Ile788Met)
c.2241C>G (p.Ile747Met)
19g.41970475G=CA2336720990ATP1A3c.2370C= (p.Ile790=)
c.2331C= (p.Ile777=)
c.2364C= (p.Ile788=)
c.2241C= (p.Ile747=)
19g.41970475G>TCA507694844ATP1A3c.2370C>A (p.Ile790=)
c.2331C>A (p.Ile777=)
c.2364C>A (p.Ile788=)
c.2241C>A (p.Ile747=)
19g.41970476A=CA2336720992ATP1A3c.2369T= (p.Ile790=)
c.2330T= (p.Ile777=)
c.2363T= (p.Ile788=)
c.2240T= (p.Ile747=)
19g.41970476A>CCA406039556ATP1A3c.2369T>G (p.Ile790Ser)
c.2330T>G (p.Ile777Ser)
c.2363T>G (p.Ile788Ser)
c.2240T>G (p.Ile747Ser)
19g.41970476A>GCA406039558ATP1A3c.2369T>C (p.Ile790Thr)
c.2330T>C (p.Ile777Thr)
c.2363T>C (p.Ile788Thr)
c.2240T>C (p.Ile747Thr)
19g.41970476A>TCA406039560ATP1A3c.2369T>A (p.Ile790Asn)
c.2330T>A (p.Ile777Asn)
c.2363T>A (p.Ile788Asn)
c.2240T>A (p.Ile747Asn)
 ClinVar dbSNP
19g.41970477T>ACA406039562ATP1A3c.2368A>T (p.Ile790Phe)
c.2329A>T (p.Ile777Phe)
c.2362A>T (p.Ile788Phe)
c.2239A>T (p.Ile747Phe)
19g.41970477T>CCA406039563ATP1A3c.2368A>G (p.Ile790Val)
c.2329A>G (p.Ile777Val)
c.2362A>G (p.Ile788Val)
c.2239A>G (p.Ile747Val)
19g.41970477T>GCA406039565ATP1A3c.2368A>C (p.Ile790Leu)
c.2329A>C (p.Ile777Leu)
c.2362A>C (p.Ile788Leu)
c.2239A>C (p.Ile747Leu)
19g.41970478C>ACA406039567ATP1A3c.2367G>T (p.Glu789Asp)
c.2328G>T (p.Glu776Asp)
c.2361G>T (p.Glu787Asp)
c.2238G>T (p.Glu746Asp)
19g.41970478C=CA2336720999ATP1A3c.2367G= (p.Glu789=)
c.2328G= (p.Glu776=)
c.2361G= (p.Glu787=)
c.2238G= (p.Glu746=)
19g.41970478C>GCA406039568ATP1A3c.2367G>C (p.Glu789Asp)
c.2328G>C (p.Glu776Asp)
c.2361G>C (p.Glu787Asp)
c.2238G>C (p.Glu746Asp)
 ClinVar dbSNP
19g.41970478C>TCA507694845ATP1A3c.2367G>A (p.Glu789=)
c.2328G>A (p.Glu776=)
c.2361G>A (p.Glu787=)
c.2238G>A (p.Glu746=)
19g.41970479T>ACA406039570ATP1A3c.2366A>T (p.Glu789Val)
c.2327A>T (p.Glu776Val)
c.2360A>T (p.Glu787Val)
c.2237A>T (p.Glu746Val)
19g.41970479T>CCA406039571ATP1A3c.2366A>G (p.Glu789Gly)
c.2327A>G (p.Glu776Gly)
c.2360A>G (p.Glu787Gly)
c.2237A>G (p.Glu746Gly)
19g.41970479T>GCA406039573ATP1A3c.2366A>C (p.Glu789Ala)
c.2327A>C (p.Glu776Ala)
c.2360A>C (p.Glu787Ala)
c.2237A>C (p.Glu746Ala)
19g.41970480C>ACA406039578ATP1A3c.2365G>T (p.Glu789Ter)
c.2326G>T (p.Glu776Ter)
c.2359G>T (p.Glu787Ter)
c.2236G>T (p.Glu746Ter)
19g.41970480C>GCA406039575ATP1A3c.2365G>C (p.Glu789Gln)
c.2326G>C (p.Glu776Gln)
c.2359G>C (p.Glu787Gln)
c.2236G>C (p.Glu746Gln)
19g.41970480C>TCA406039577ATP1A3c.2365G>A (p.Glu789Lys)
c.2326G>A (p.Glu776Lys)
c.2359G>A (p.Glu787Lys)
c.2236G>A (p.Glu746Lys)
 ClinVar dbSNP
19g.41970481C>ACA507583158ATP1A3c.2364G>T (p.Pro788=)
c.2325G>T (p.Pro775=)
c.2358G>T (p.Pro786=)
c.2235G>T (p.Pro745=)
19g.41970481C=CA2336721003ATP1A3c.2364G= (p.Pro788=)
c.2325G= (p.Pro775=)
c.2358G= (p.Pro786=)
c.2235G= (p.Pro745=)
19g.41970481C>GCA507583159ATP1A3c.2364G>C (p.Pro788=)
c.2325G>C (p.Pro775=)
c.2358G>C (p.Pro786=)
c.2235G>C (p.Pro745=)
 ClinVar dbSNP
19g.41970481C>TCA9467414ATP1A3c.2364G>A (p.Pro788=)
c.2325G>A (p.Pro775=)
c.2358G>A (p.Pro786=)
c.2235G>A (p.Pro745=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.41970482G>ACA10603656ATP1A3c.2363C>T (p.Pro788Leu)
c.2324C>T (p.Pro775Leu)
c.2357C>T (p.Pro786Leu)
c.2234C>T (p.Pro745Leu)
 ClinVar dbSNP
19g.41970482G>CCA406039582ATP1A3c.2363C>G (p.Pro788Arg)
c.2324C>G (p.Pro775Arg)
c.2357C>G (p.Pro786Arg)
c.2234C>G (p.Pro745Arg)
19g.41970482G=CA2336721008ATP1A3c.2363C= (p.Pro788=)
c.2324C= (p.Pro775=)
c.2357C= (p.Pro786=)
c.2234C= (p.Pro745=)
19g.41970482G>TCA406039583ATP1A3c.2363C>A (p.Pro788Gln)
c.2324C>A (p.Pro775Gln)
c.2357C>A (p.Pro786Gln)
c.2234C>A (p.Pro745Gln)
19g.41970483G>ACA406039585ATP1A3c.2362C>T (p.Pro788Ser)
c.2323C>T (p.Pro775Ser)
c.2356C>T (p.Pro786Ser)
c.2233C>T (p.Pro745Ser)
19g.41970483G>CCA406039587ATP1A3c.2362C>G (p.Pro788Ala)
c.2323C>G (p.Pro775Ala)
c.2356C>G (p.Pro786Ala)
c.2233C>G (p.Pro745Ala)
19g.41970483G=CA2336721014ATP1A3c.2362C= (p.Pro788=)
c.2323C= (p.Pro775=)
c.2356C= (p.Pro786=)
c.2233C= (p.Pro745=)
19g.41970483G>TCA406039589ATP1A3c.2362C>A (p.Pro788Thr)
c.2323C>A (p.Pro775Thr)
c.2356C>A (p.Pro786Thr)
c.2233C>A (p.Pro745Thr)
 ClinVar dbSNP
19g.41970484G>ACA507583164ATP1A3c.2361C>T (p.Ile787=)
c.2322C>T (p.Ile774=)
c.2355C>T (p.Ile785=)
c.2232C>T (p.Ile744=)
 gnomAD v4
19g.41970484G>CCA406039590ATP1A3c.2361C>G (p.Ile787Met)
c.2322C>G (p.Ile774Met)
c.2355C>G (p.Ile785Met)
c.2232C>G (p.Ile744Met)
19g.41970484G=CA2336721016ATP1A3c.2361C= (p.Ile787=)
c.2322C= (p.Ile774=)
c.2355C= (p.Ile785=)
c.2232C= (p.Ile744=)
19g.41970484G>TCA507583165ATP1A3c.2361C>A (p.Ile787=)
c.2322C>A (p.Ile774=)
c.2355C>A (p.Ile785=)
c.2232C>A (p.Ile744=)
 dbSNP
19g.41970485A>CCA406039593ATP1A3c.2360T>G (p.Ile787Ser)
c.2321T>G (p.Ile774Ser)
c.2354T>G (p.Ile785Ser)
c.2231T>G (p.Ile744Ser)
19g.41970485A>GCA406039594ATP1A3c.2360T>C (p.Ile787Thr)
c.2321T>C (p.Ile774Thr)
c.2354T>C (p.Ile785Thr)
c.2231T>C (p.Ile744Thr)
19g.41970485A>TCA406039596ATP1A3c.2360T>A (p.Ile787Asn)
c.2321T>A (p.Ile774Asn)
c.2354T>A (p.Ile785Asn)
c.2231T>A (p.Ile744Asn)
19g.41970486T>ACA406039597ATP1A3c.2359A>T (p.Ile787Phe)
c.2320A>T (p.Ile774Phe)
c.2353A>T (p.Ile785Phe)
c.2230A>T (p.Ile744Phe)
19g.41970486T>CCA9467415ATP1A3c.2359A>G (p.Ile787Val)
c.2320A>G (p.Ile774Val)
c.2353A>G (p.Ile785Val)
c.2230A>G (p.Ile744Val)
 dbSNP ExAC gnomAD v2 gnomAD v4
19g.41970486T>GCA406039598ATP1A3c.2359A>C (p.Ile787Leu)
c.2320A>C (p.Ile774Leu)
c.2353A>C (p.Ile785Leu)
c.2230A>C (p.Ile744Leu)
19g.41970486T=CA2336721019ATP1A3c.2359A= (p.Ile787=)
c.2320A= (p.Ile774=)
c.2353A= (p.Ile785=)
c.2230A= (p.Ile744=)
19g.41970487A=CA2336721024ATP1A3c.2358T= (p.Asn786=)
c.2319T= (p.Asn773=)
c.2352T= (p.Asn784=)
c.2229T= (p.Asn743=)
19g.41970487A>CCA406039601ATP1A3c.2358T>G (p.Asn786Lys)
c.2319T>G (p.Asn773Lys)
c.2352T>G (p.Asn784Lys)
c.2229T>G (p.Asn743Lys)
19g.41970487A>GCA171285ATP1A3c.2358T>C (p.Asn786=)
c.2319T>C (p.Asn773=)
c.2352T>C (p.Asn784=)
c.2229T>C (p.Asn743=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.41970487A>TCA406039603ATP1A3c.2358T>A (p.Asn786Lys)
c.2319T>A (p.Asn773Lys)
c.2352T>A (p.Asn784Lys)
c.2229T>A (p.Asn743Lys)
19g.41970488T>ACA346022ATP1A3c.2357A>T (p.Asn786Ile)
c.2318A>T (p.Asn773Ile)
c.2351A>T (p.Asn784Ile)
c.2228A>T (p.Asn743Ile)
 dbSNP
19g.41970488T>CCA346021ATP1A3c.2357A>G (p.Asn786Ser)
c.2318A>G (p.Asn773Ser)
c.2351A>G (p.Asn784Ser)
c.2228A>G (p.Asn743Ser)
 ClinVar dbSNP
19g.41970488T>GCA406039607ATP1A3c.2357A>C (p.Asn786Thr)
c.2318A>C (p.Asn773Thr)
c.2351A>C (p.Asn784Thr)
c.2228A>C (p.Asn743Thr)
19g.41970488T=CA2336721029ATP1A3c.2357A= (p.Asn786=)
c.2318A= (p.Asn773=)
c.2351A= (p.Asn784=)
c.2228A= (p.Asn743=)
19g.41970489T>ACA406039609ATP1A3c.2356A>T (p.Asn786Tyr)
c.2317A>T (p.Asn773Tyr)
c.2350A>T (p.Asn784Tyr)
c.2227A>T (p.Asn743Tyr)
19g.41970489T>CCA406039610ATP1A3c.2356A>G (p.Asn786Asp)
c.2317A>G (p.Asn773Asp)
c.2350A>G (p.Asn784Asp)
c.2227A>G (p.Asn743Asp)
19g.41970489T>GCA406039611ATP1A3c.2356A>C (p.Asn786His)
c.2317A>C (p.Asn773His)
c.2350A>C (p.Asn784His)
c.2227A>C (p.Asn743His)
19g.41970490G>ACA507583171ATP1A3c.2355C>T (p.Ser785=)
c.2316C>T (p.Ser772=)
c.2349C>T (p.Ser783=)
c.2226C>T (p.Ser742=)
19g.41970490G>CCA308586631ATP1A3c.2355C>G (p.Ser785Arg)
c.2316C>G (p.Ser772Arg)
c.2349C>G (p.Ser783Arg)
c.2226C>G (p.Ser742Arg)
 dbSNP
19g.41970490G=CA2336721032ATP1A3c.2355C= (p.Ser785=)
c.2316C= (p.Ser772=)
c.2349C= (p.Ser783=)
c.2226C= (p.Ser742=)
19g.41970490G>TCA346020ATP1A3c.2355C>A (p.Ser785Arg)
c.2316C>A (p.Ser772Arg)
c.2349C>A (p.Ser783Arg)
c.2226C>A (p.Ser742Arg)
 dbSNP
19g.41970491C>ACA406039613ATP1A3c.2354G>T (p.Ser785Ile)
c.2315G>T (p.Ser772Ile)
c.2348G>T (p.Ser783Ile)
c.2225G>T (p.Ser742Ile)
19g.41970491C=CA2336721036ATP1A3c.2354G= (p.Ser785=)
c.2315G= (p.Ser772=)
c.2348G= (p.Ser783=)
c.2225G= (p.Ser742=)
19g.41970491C>GCA406039614ATP1A3c.2354G>C (p.Ser785Thr)
c.2315G>C (p.Ser772Thr)
c.2348G>C (p.Ser783Thr)
c.2225G>C (p.Ser742Thr)
19g.41970491C>TCA16620856ATP1A3c.2354G>A (p.Ser785Asn)
c.2315G>A (p.Ser772Asn)
c.2348G>A (p.Ser783Asn)
c.2225G>A (p.Ser742Asn)
 ClinVar dbSNP
19g.41970492T>ACA406039619ATP1A3c.2353A>T (p.Ser785Cys)
c.2314A>T (p.Ser772Cys)
c.2347A>T (p.Ser783Cys)
c.2224A>T (p.Ser742Cys)
19g.41970492T>CCA406039617ATP1A3c.2353A>G (p.Ser785Gly)
c.2314A>G (p.Ser772Gly)
c.2347A>G (p.Ser783Gly)
c.2224A>G (p.Ser742Gly)
19g.41970492T>GCA406039616ATP1A3c.2353A>C (p.Ser785Arg)
c.2314A>C (p.Ser772Arg)
c.2347A>C (p.Ser783Arg)
c.2224A>C (p.Ser742Arg)
19g.41970493G>ACA507583172ATP1A3c.2352C>T (p.Thr784=)
c.2313C>T (p.Thr771=)
c.2346C>T (p.Thr782=)
c.2223C>T (p.Thr741=)
 gnomAD v4
19g.41970493G>CCA507583173ATP1A3c.2352C>G (p.Thr784=)
c.2313C>G (p.Thr771=)
c.2346C>G (p.Thr782=)
c.2223C>G (p.Thr741=)
19g.41970493G>TCA507583174ATP1A3c.2352C>A (p.Thr784=)
c.2313C>A (p.Thr771=)
c.2346C>A (p.Thr782=)
c.2223C>A (p.Thr741=)
19g.41970494G>ACA308586633ATP1A3c.2351C>T (p.Thr784Ile)
c.2312C>T (p.Thr771Ile)
c.2345C>T (p.Thr782Ile)
c.2222C>T (p.Thr741Ile)
 ClinVar dbSNP
19g.41970494G>CCA406039621ATP1A3c.2351C>G (p.Thr784Ser)
c.2312C>G (p.Thr771Ser)
c.2345C>G (p.Thr782Ser)
c.2222C>G (p.Thr741Ser)
19g.41970494G=CA2336721041ATP1A3c.2351C= (p.Thr784=)
c.2312C= (p.Thr771=)
c.2345C= (p.Thr782=)
c.2222C= (p.Thr741=)
19g.41970494G>TCA346018ATP1A3c.2351C>A (p.Thr784Asn)
c.2312C>A (p.Thr771Asn)
c.2345C>A (p.Thr782Asn)
c.2222C>A (p.Thr741Asn)
 dbSNP
19g.41970495T>ACA406039624ATP1A3c.2350A>T (p.Thr784Ser)
c.2311A>T (p.Thr771Ser)
c.2344A>T (p.Thr782Ser)
c.2221A>T (p.Thr741Ser)
19g.41970495T>CCA406039625ATP1A3c.2350A>G (p.Thr784Ala)
c.2311A>G (p.Thr771Ala)
c.2344A>G (p.Thr782Ala)
c.2221A>G (p.Thr741Ala)
19g.41970495T>GCA406039627ATP1A3c.2350A>C (p.Thr784Pro)
c.2311A>C (p.Thr771Pro)
c.2344A>C (p.Thr782Pro)
c.2221A>C (p.Thr741Pro)
19g.41970496C>ACA507583178ATP1A3c.2349G>T (p.Leu783=)
c.2310G>T (p.Leu770=)
c.2343G>T (p.Leu781=)
c.2220G>T (p.Leu740=)
19g.41970496C=CA2336721045ATP1A3c.2349G= (p.Leu783=)
c.2310G= (p.Leu770=)
c.2343G= (p.Leu781=)
c.2220G= (p.Leu740=)
19g.41970496C>GCA507583179ATP1A3c.2349G>C (p.Leu783=)
c.2310G>C (p.Leu770=)
c.2343G>C (p.Leu781=)
c.2220G>C (p.Leu740=)
19g.41970496C>TCA308586637ATP1A3c.2349G>A (p.Leu783=)
c.2310G>A (p.Leu770=)
c.2343G>A (p.Leu781=)
c.2220G>A (p.Leu740=)
 dbSNP
19g.41970497A=CA2336721049ATP1A3c.2348T= (p.Leu783=)
c.2309T= (p.Leu770=)
c.2342T= (p.Leu781=)
c.2219T= (p.Leu740=)
19g.41970497A>CCA308586643ATP1A3c.2348T>G (p.Leu783Arg)
c.2309T>G (p.Leu770Arg)
c.2342T>G (p.Leu781Arg)
c.2219T>G (p.Leu740Arg)
 ClinVar dbSNP
19g.41970497A>GCA406039630ATP1A3c.2348T>C (p.Leu783Pro)
c.2309T>C (p.Leu770Pro)
c.2342T>C (p.Leu781Pro)
c.2219T>C (p.Leu740Pro)
19g.41970497A>TCA406039632ATP1A3c.2348T>A (p.Leu783Gln)
c.2309T>A (p.Leu770Gln)
c.2342T>A (p.Leu781Gln)
c.2219T>A (p.Leu740Gln)
19g.41970498G>ACA507583181ATP1A3c.2347C>T (p.Leu783=)
c.2308C>T (p.Leu770=)
c.2341C>T (p.Leu781=)
c.2218C>T (p.Leu740=)
 dbSNP
19g.41970498G>CCA406039634ATP1A3c.2347C>G (p.Leu783Val)
c.2308C>G (p.Leu770Val)
c.2341C>G (p.Leu781Val)
c.2218C>G (p.Leu740Val)
19g.41970498G=CA2336721051ATP1A3c.2347C= (p.Leu783=)
c.2308C= (p.Leu770=)
c.2341C= (p.Leu781=)
c.2218C= (p.Leu740=)
19g.41970498G>TCA406039636ATP1A3c.2347C>A (p.Leu783Met)
c.2308C>A (p.Leu770Met)
c.2341C>A (p.Leu781Met)
c.2218C>A (p.Leu740Met)
19g.41970499G>ACA10648759ATP1A3c.2346C>T (p.Thr782=)
c.2307C>T (p.Thr769=)
c.2340C>T (p.Thr780=)
c.2217C>T (p.Thr739=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41970499G>CCA507583183ATP1A3c.2346C>G (p.Thr782=)
c.2307C>G (p.Thr769=)
c.2340C>G (p.Thr780=)
c.2217C>G (p.Thr739=)
19g.41970499G=CA2336721053ATP1A3c.2346C= (p.Thr782=)
c.2307C= (p.Thr769=)
c.2340C= (p.Thr780=)
c.2217C= (p.Thr739=)
19g.41970499G>TCA507583185ATP1A3c.2346C>A (p.Thr782=)
c.2307C>A (p.Thr769=)
c.2340C>A (p.Thr780=)
c.2217C>A (p.Thr739=)
19g.41970500G>ACA406039642ATP1A3c.2345C>T (p.Thr782Ile)
c.2306C>T (p.Thr769Ile)
c.2339C>T (p.Thr780Ile)
c.2216C>T (p.Thr739Ile)
19g.41970500G>CCA406039639ATP1A3c.2345C>G (p.Thr782Ser)
c.2306C>G (p.Thr769Ser)
c.2339C>G (p.Thr780Ser)
c.2216C>G (p.Thr739Ser)
19g.41970500G>TCA406039640ATP1A3c.2345C>A (p.Thr782Asn)
c.2306C>A (p.Thr769Asn)
c.2339C>A (p.Thr780Asn)
c.2216C>A (p.Thr739Asn)
19g.41970501T>ACA406039643ATP1A3c.2344A>T (p.Thr782Ser)
c.2305A>T (p.Thr769Ser)
c.2338A>T (p.Thr780Ser)
c.2215A>T (p.Thr739Ser)
 gnomAD v4
19g.41970501T>CCA406039644ATP1A3c.2344A>G (p.Thr782Ala)
c.2305A>G (p.Thr769Ala)
c.2338A>G (p.Thr780Ala)
c.2215A>G (p.Thr739Ala)
19g.41970501T>GCA406039646ATP1A3c.2344A>C (p.Thr782Pro)
c.2305A>C (p.Thr769Pro)
c.2338A>C (p.Thr780Pro)
c.2215A>C (p.Thr739Pro)
19g.41970502G>ACA507583189ATP1A3c.2343C>T (p.Tyr781=)
c.2304C>T (p.Tyr768=)
c.2337C>T (p.Tyr779=)
c.2214C>T (p.Tyr738=)
 dbSNP gnomAD v2 gnomAD v4
19g.41970502G>CCA406039648ATP1A3c.2343C>G (p.Tyr781Ter)
c.2304C>G (p.Tyr768Ter)
c.2337C>G (p.Tyr779Ter)
c.2214C>G (p.Tyr738Ter)
19g.41970502G=CA2336721054ATP1A3c.2343C= (p.Tyr781=)
c.2304C= (p.Tyr768=)
c.2337C= (p.Tyr779=)
c.2214C= (p.Tyr738=)
19g.41970502G>TCA406039649ATP1A3c.2343C>A (p.Tyr781Ter)
c.2304C>A (p.Tyr768Ter)
c.2337C>A (p.Tyr779Ter)
c.2214C>A (p.Tyr738Ter)
19g.41970503T>ACA406039651ATP1A3c.2342A>T (p.Tyr781Phe)
c.2303A>T (p.Tyr768Phe)
c.2336A>T (p.Tyr779Phe)
c.2213A>T (p.Tyr738Phe)
19g.41970503T>CCA406039653ATP1A3c.2342A>G (p.Tyr781Cys)
c.2303A>G (p.Tyr768Cys)
c.2336A>G (p.Tyr779Cys)
c.2213A>G (p.Tyr738Cys)
 ClinVar dbSNP
19g.41970503T>GCA406039654ATP1A3c.2342A>C (p.Tyr781Ser)
c.2303A>C (p.Tyr768Ser)
c.2336A>C (p.Tyr779Ser)
c.2213A>C (p.Tyr738Ser)
19g.41970503T=CA2336721056ATP1A3c.2342A= (p.Tyr781=)
c.2303A= (p.Tyr768=)
c.2336A= (p.Tyr779=)
c.2213A= (p.Tyr738=)
19g.41970504A>CCA406039656ATP1A3c.2341T>G (p.Tyr781Asp)
c.2302T>G (p.Tyr768Asp)
c.2335T>G (p.Tyr779Asp)
c.2212T>G (p.Tyr738Asp)
19g.41970504A>GCA406039657ATP1A3c.2341T>C (p.Tyr781His)
c.2302T>C (p.Tyr768His)
c.2335T>C (p.Tyr779His)
c.2212T>C (p.Tyr738His)
 ClinVar
19g.41970504A>TCA406039659ATP1A3c.2341T>A (p.Tyr781Asn)
c.2302T>A (p.Tyr768Asn)
c.2335T>A (p.Tyr779Asn)
c.2212T>A (p.Tyr738Asn)
19g.41970505G>ACA507583195ATP1A3c.2340C>T (p.Ala780=)
c.2301C>T (p.Ala767=)
c.2334C>T (p.Ala778=)
c.2211C>T (p.Ala737=)
19g.41970505G>CCA507583193ATP1A3c.2340C>G (p.Ala780=)
c.2301C>G (p.Ala767=)
c.2334C>G (p.Ala778=)
c.2211C>G (p.Ala737=)
19g.41970505G=CA2336721061ATP1A3c.2340C= (p.Ala780=)
c.2301C= (p.Ala767=)
c.2334C= (p.Ala778=)
c.2211C= (p.Ala737=)
19g.41970505G>TCA507583194ATP1A3c.2340C>A (p.Ala780=)
c.2301C>A (p.Ala767=)
c.2334C>A (p.Ala778=)
c.2211C>A (p.Ala737=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41970506G>ACA406039664ATP1A3c.2339C>T (p.Ala780Val)
c.2300C>T (p.Ala767Val)
c.2333C>T (p.Ala778Val)
c.2210C>T (p.Ala737Val)
 gnomAD v4
19g.41970506G>CCA406039661ATP1A3c.2339C>G (p.Ala780Gly)
c.2300C>G (p.Ala767Gly)
c.2333C>G (p.Ala778Gly)
c.2210C>G (p.Ala737Gly)
19g.41970506G>TCA406039663ATP1A3c.2339C>A (p.Ala780Asp)
c.2300C>A (p.Ala767Asp)
c.2333C>A (p.Ala778Asp)
c.2210C>A (p.Ala737Asp)
19g.41970507C>ACA406039666ATP1A3c.2338G>T (p.Ala780Ser)
c.2299G>T (p.Ala767Ser)
c.2332G>T (p.Ala778Ser)
c.2209G>T (p.Ala737Ser)
19g.41970507C>GCA406039668ATP1A3c.2338G>C (p.Ala780Pro)
c.2299G>C (p.Ala767Pro)
c.2332G>C (p.Ala778Pro)
c.2209G>C (p.Ala737Pro)
19g.41970507C>TCA406039669ATP1A3c.2338G>A (p.Ala780Thr)
c.2299G>A (p.Ala767Thr)
c.2332G>A (p.Ala778Thr)
c.2209G>A (p.Ala737Thr)
19g.41970508A>CCA406039671ATP1A3c.2337T>G (p.Ile779Met)
c.2298T>G (p.Ile766Met)
c.2331T>G (p.Ile777Met)
c.2208T>G (p.Ile736Met)
19g.41970508A>GCA507583199ATP1A3c.2337T>C (p.Ile779=)
c.2298T>C (p.Ile766=)
c.2331T>C (p.Ile777=)
c.2208T>C (p.Ile736=)
19g.41970508A>TCA507583198ATP1A3c.2337T>A (p.Ile779=)
c.2298T>A (p.Ile766=)
c.2331T>A (p.Ile777=)
c.2208T>A (p.Ile736=)
19g.41970509A>CCA406039673ATP1A3c.2336T>G (p.Ile779Ser)
c.2297T>G (p.Ile766Ser)
c.2330T>G (p.Ile777Ser)
c.2207T>G (p.Ile736Ser)
19g.41970509A>GCA406039674ATP1A3c.2336T>C (p.Ile779Thr)
c.2297T>C (p.Ile766Thr)
c.2330T>C (p.Ile777Thr)
c.2207T>C (p.Ile736Thr)
 gnomAD v4
19g.41970509A>TCA406039676ATP1A3c.2336T>A (p.Ile779Asn)
c.2297T>A (p.Ile766Asn)
c.2330T>A (p.Ile777Asn)
c.2207T>A (p.Ile736Asn)
19g.41970510T>ACA406039677ATP1A3c.2335A>T (p.Ile779Phe)
c.2296A>T (p.Ile766Phe)
c.2329A>T (p.Ile777Phe)
c.2206A>T (p.Ile736Phe)
19g.41970510T>CCA406039679ATP1A3c.2335A>G (p.Ile779Val)
c.2296A>G (p.Ile766Val)
c.2329A>G (p.Ile777Val)
c.2206A>G (p.Ile736Val)
19g.41970510T>GCA406039681ATP1A3c.2335A>C (p.Ile779Leu)
c.2296A>C (p.Ile766Leu)
c.2329A>C (p.Ile777Leu)
c.2206A>C (p.Ile736Leu)
19g.41970511G>ACA9467416ATP1A3c.2334C>T (p.Ser778=)
c.2295C>T (p.Ser765=)
c.2328C>T (p.Ser776=)
c.2205C>T (p.Ser735=)
 dbSNP ExAC gnomAD v3 gnomAD v4
19g.41970511G>CCA507583208ATP1A3c.2334C>G (p.Ser778=)
c.2295C>G (p.Ser765=)
c.2328C>G (p.Ser776=)
c.2205C>G (p.Ser735=)
19g.41970511G=CA2336721063ATP1A3c.2334C= (p.Ser778=)
c.2295C= (p.Ser765=)
c.2328C= (p.Ser776=)
c.2205C= (p.Ser735=)
19g.41970511G>TCA507583207ATP1A3c.2334C>A (p.Ser778=)
c.2295C>A (p.Ser765=)
c.2328C>A (p.Ser776=)
c.2205C>A (p.Ser735=)
19g.41970512G>ACA406039686ATP1A3c.2333C>T (p.Ser778Phe)
c.2294C>T (p.Ser765Phe)
c.2327C>T (p.Ser776Phe)
c.2204C>T (p.Ser735Phe)
19g.41970512G>CCA406039685ATP1A3c.2333C>G (p.Ser778Cys)
c.2294C>G (p.Ser765Cys)
c.2327C>G (p.Ser776Cys)
c.2204C>G (p.Ser735Cys)
19g.41970512G>TCA406039683ATP1A3c.2333C>A (p.Ser778Tyr)
c.2294C>A (p.Ser765Tyr)
c.2327C>A (p.Ser776Tyr)
c.2204C>A (p.Ser735Tyr)
19g.41970513A>CCA406039688ATP1A3c.2332T>G (p.Ser778Ala)
c.2293T>G (p.Ser765Ala)
c.2326T>G (p.Ser776Ala)
c.2203T>G (p.Ser735Ala)
19g.41970513A>GCA406039689ATP1A3c.2332T>C (p.Ser778Pro)
c.2293T>C (p.Ser765Pro)
c.2326T>C (p.Ser776Pro)
c.2203T>C (p.Ser735Pro)
19g.41970513A>TCA406039690ATP1A3c.2332T>A (p.Ser778Thr)
c.2293T>A (p.Ser765Thr)
c.2326T>A (p.Ser776Thr)
c.2203T>A (p.Ser735Thr)
19g.41970514C>ACA406039692ATP1A3c.2331G>T (p.Lys777Asn)
c.2292G>T (p.Lys764Asn)
c.2325G>T (p.Lys775Asn)
c.2202G>T (p.Lys734Asn)
19g.41970514C>GCA406039694ATP1A3c.2331G>C (p.Lys777Asn)
c.2292G>C (p.Lys764Asn)
c.2325G>C (p.Lys775Asn)
c.2202G>C (p.Lys734Asn)
19g.41970514C>TCA507583211ATP1A3c.2331G>A (p.Lys777=)
c.2292G>A (p.Lys764=)
c.2325G>A (p.Lys775=)
c.2202G>A (p.Lys734=)
19g.41970517_41970519delCA2573105901ATP1A3c.2329_2331del (p.Lys777del)
c.2290_2292del (p.Lys764del)
c.2323_2325del (p.Lys775del)
c.2200_2202del (p.Lys734del)
19g.41970515T>ACA406039695ATP1A3c.2330A>T (p.Lys777Met)
c.2291A>T (p.Lys764Met)
c.2324A>T (p.Lys775Met)
c.2201A>T (p.Lys734Met)
19g.41970515T>CCA406039697ATP1A3c.2330A>G (p.Lys777Arg)
c.2291A>G (p.Lys764Arg)
c.2324A>G (p.Lys775Arg)
c.2201A>G (p.Lys734Arg)
19g.41970515T>GCA406039698ATP1A3c.2330A>C (p.Lys777Thr)
c.2291A>C (p.Lys764Thr)
c.2324A>C (p.Lys775Thr)
c.2201A>C (p.Lys734Thr)
19g.41970516T>ACA406039700ATP1A3c.2329A>T (p.Lys777Ter)
c.2290A>T (p.Lys764Ter)
c.2323A>T (p.Lys775Ter)
c.2200A>T (p.Lys734Ter)
19g.41970516T>CCA406039701ATP1A3c.2329A>G (p.Lys777Glu)
c.2290A>G (p.Lys764Glu)
c.2323A>G (p.Lys775Glu)
c.2200A>G (p.Lys734Glu)
19g.41970516T>GCA406039703ATP1A3c.2329A>C (p.Lys777Gln)
c.2290A>C (p.Lys764Gln)
c.2323A>C (p.Lys775Gln)
c.2200A>C (p.Lys734Gln)
19g.41970517C>ACA406039704ATP1A3c.2328G>T (p.Lys776Asn)
c.2289G>T (p.Lys763Asn)
c.2322G>T (p.Lys774Asn)
c.2199G>T (p.Lys733Asn)
19g.41970517C>GCA406039706ATP1A3c.2328G>C (p.Lys776Asn)
c.2289G>C (p.Lys763Asn)
c.2322G>C (p.Lys774Asn)
c.2199G>C (p.Lys733Asn)
19g.41970517C>TCA507583218ATP1A3c.2328G>A (p.Lys776=)
c.2289G>A (p.Lys763=)
c.2322G>A (p.Lys774=)
c.2199G>A (p.Lys733=)
19g.41970518T>ACA406039711ATP1A3c.2327A>T (p.Lys776Met)
c.2288A>T (p.Lys763Met)
c.2321A>T (p.Lys774Met)
c.2198A>T (p.Lys733Met)
19g.41970518T>CCA406039709ATP1A3c.2327A>G (p.Lys776Arg)
c.2288A>G (p.Lys763Arg)
c.2321A>G (p.Lys774Arg)
c.2198A>G (p.Lys733Arg)
19g.41970518T>GCA406039708ATP1A3c.2327A>C (p.Lys776Thr)
c.2288A>C (p.Lys763Thr)
c.2321A>C (p.Lys774Thr)
c.2198A>C (p.Lys733Thr)
19g.41970519T>ACA406039713ATP1A3c.2326A>T (p.Lys776Ter)
c.2287A>T (p.Lys763Ter)
c.2320A>T (p.Lys774Ter)
c.2197A>T (p.Lys733Ter)
19g.41970519T>CCA406039714ATP1A3c.2326A>G (p.Lys776Glu)
c.2287A>G (p.Lys763Glu)
c.2320A>G (p.Lys774Glu)
c.2197A>G (p.Lys733Glu)
19g.41970519T>GCA406039716ATP1A3c.2326A>C (p.Lys776Gln)
c.2287A>C (p.Lys763Gln)
c.2320A>C (p.Lys774Gln)
c.2197A>C (p.Lys733Gln)
19g.41970520T>ACA507583227ATP1A3c.2325A>T (p.Leu775=)
c.2286A>T (p.Leu762=)
c.2319A>T (p.Leu773=)
c.2196A>T (p.Leu732=)
19g.41970520T>CCA507583228ATP1A3c.2325A>G (p.Leu775=)
c.2286A>G (p.Leu762=)
c.2319A>G (p.Leu773=)
c.2196A>G (p.Leu732=)
19g.41970520T>GCA507583229ATP1A3c.2325A>C (p.Leu775=)
c.2286A>C (p.Leu762=)
c.2319A>C (p.Leu773=)
c.2196A>C (p.Leu732=)
19g.41970521A>CCA406039717ATP1A3c.2324T>G (p.Leu775Arg)
c.2285T>G (p.Leu762Arg)
c.2318T>G (p.Leu773Arg)
c.2195T>G (p.Leu732Arg)
19g.41970521A>GCA406039719ATP1A3c.2324T>C (p.Leu775Pro)
c.2285T>C (p.Leu762Pro)
c.2318T>C (p.Leu773Pro)
c.2195T>C (p.Leu732Pro)
19g.41970521A>TCA406039720ATP1A3c.2324T>A (p.Leu775Gln)
c.2285T>A (p.Leu762Gln)
c.2318T>A (p.Leu773Gln)
c.2195T>A (p.Leu732Gln)
19g.41970522G>ACA507583233ATP1A3c.2323C>T (p.Leu775=)
c.2284C>T (p.Leu762=)
c.2317C>T (p.Leu773=)
c.2194C>T (p.Leu732=)
19g.41970522G>CCA406039722ATP1A3c.2323C>G (p.Leu775Val)
c.2284C>G (p.Leu762Val)
c.2317C>G (p.Leu773Val)
c.2194C>G (p.Leu732Val)
19g.41970522G>TCA406039724ATP1A3c.2323C>A (p.Leu775Ile)
c.2284C>A (p.Leu762Ile)
c.2317C>A (p.Leu773Ile)
c.2194C>A (p.Leu732Ile)
19g.41970523G>ACA308586654ATP1A3c.2322C>T (p.Asn774=)
c.2283C>T (p.Asn761=)
c.2316C>T (p.Asn772=)
c.2193C>T (p.Asn731=)
 dbSNP gnomAD v3 gnomAD v4
19g.41970523G>CCA406039725ATP1A3c.2322C>G (p.Asn774Lys)
c.2283C>G (p.Asn761Lys)
c.2316C>G (p.Asn772Lys)
c.2193C>G (p.Asn731Lys)
19g.41970523G=CA2336721065ATP1A3c.2322C= (p.Asn774=)
c.2283C= (p.Asn761=)
c.2316C= (p.Asn772=)
c.2193C= (p.Asn731=)
19g.41970523G>TCA406039727ATP1A3c.2322C>A (p.Asn774Lys)
c.2283C>A (p.Asn761Lys)
c.2316C>A (p.Asn772Lys)
c.2193C>A (p.Asn731Lys)
19g.41970524T>ACA406039729ATP1A3c.2321A>T (p.Asn774Ile)
c.2282A>T (p.Asn761Ile)
c.2315A>T (p.Asn772Ile)
c.2192A>T (p.Asn731Ile)
19g.41970524T>CCA406039731ATP1A3c.2321A>G (p.Asn774Ser)
c.2282A>G (p.Asn761Ser)
c.2315A>G (p.Asn772Ser)
c.2192A>G (p.Asn731Ser)
19g.41970524T>GCA406039732ATP1A3c.2321A>C (p.Asn774Thr)
c.2282A>C (p.Asn761Thr)
c.2315A>C (p.Asn772Thr)
c.2192A>C (p.Asn731Thr)

Number of alleles fetched