Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.41970188T>ACA406038550ATP1A3c.2578A>T (p.Ile860Phe)
c.2539A>T (p.Ile847Phe)
c.2572A>T (p.Ile858Phe)
c.2449A>T (p.Ile817Phe)
19g.41970188T>CCA406038548ATP1A3c.2578A>G (p.Ile860Val)
c.2539A>G (p.Ile847Val)
c.2572A>G (p.Ile858Val)
c.2449A>G (p.Ile817Val)
19g.41970188T>GCA406038546ATP1A3c.2578A>C (p.Ile860Leu)
c.2539A>C (p.Ile847Leu)
c.2572A>C (p.Ile858Leu)
c.2449A>C (p.Ile817Leu)
19g.41970189C>ACA406038552ATP1A3c.2577G>T (p.Gln859His)
c.2538G>T (p.Gln846His)
c.2571G>T (p.Gln857His)
c.2448G>T (p.Gln816His)
19g.41970189C>GCA406038554ATP1A3c.2577G>C (p.Gln859His)
c.2538G>C (p.Gln846His)
c.2571G>C (p.Gln857His)
c.2448G>C (p.Gln816His)
gnomAD v4
19g.41970189C>TCA507694609ATP1A3c.2577G>A (p.Gln859=)
c.2538G>A (p.Gln846=)
c.2571G>A (p.Gln857=)
c.2448G>A (p.Gln816=)
19g.41970190T>ACA406038556ATP1A3c.2576A>T (p.Gln859Leu)
c.2537A>T (p.Gln846Leu)
c.2570A>T (p.Gln857Leu)
c.2447A>T (p.Gln816Leu)
19g.41970190T>CCA406038558ATP1A3c.2576A>G (p.Gln859Arg)
c.2537A>G (p.Gln846Arg)
c.2570A>G (p.Gln857Arg)
c.2447A>G (p.Gln816Arg)
19g.41970190T>GCA406038560ATP1A3c.2576A>C (p.Gln859Pro)
c.2537A>C (p.Gln846Pro)
c.2570A>C (p.Gln857Pro)
c.2447A>C (p.Gln816Pro)
19g.41970191G>ACA406038562ATP1A3c.2575C>T (p.Gln859Ter)
c.2536C>T (p.Gln846Ter)
c.2569C>T (p.Gln857Ter)
c.2446C>T (p.Gln816Ter)
19g.41970191G>CCA406038564ATP1A3c.2575C>G (p.Gln859Glu)
c.2536C>G (p.Gln846Glu)
c.2569C>G (p.Gln857Glu)
c.2446C>G (p.Gln816Glu)
19g.41970191G>TCA406038566ATP1A3c.2575C>A (p.Gln859Lys)
c.2536C>A (p.Gln846Lys)
c.2569C>A (p.Gln857Lys)
c.2446C>A (p.Gln816Lys)
19g.41970192C>ACA507694612ATP1A3c.2574G>T (p.Gly858=)
c.2535G>T (p.Gly845=)
c.2568G>T (p.Gly856=)
c.2445G>T (p.Gly815=)
19g.41970192C>GCA507694613ATP1A3c.2574G>C (p.Gly858=)
c.2535G>C (p.Gly845=)
c.2568G>C (p.Gly856=)
c.2445G>C (p.Gly815=)
19g.41970192C>TCA507694614ATP1A3c.2574G>A (p.Gly858=)
c.2535G>A (p.Gly845=)
c.2568G>A (p.Gly856=)
c.2445G>A (p.Gly815=)
19g.41970193C>ACA406038568ATP1A3c.2573G>T (p.Gly858Val)
c.2534G>T (p.Gly845Val)
c.2567G>T (p.Gly856Val)
c.2444G>T (p.Gly815Val)
19g.41970193C>GCA406038569ATP1A3c.2573G>C (p.Gly858Ala)
c.2534G>C (p.Gly845Ala)
c.2567G>C (p.Gly856Ala)
c.2444G>C (p.Gly815Ala)
19g.41970193C>TCA406038571ATP1A3c.2573G>A (p.Gly858Glu)
c.2534G>A (p.Gly845Glu)
c.2567G>A (p.Gly856Glu)
c.2444G>A (p.Gly815Glu)
gnomAD v4
19g.41970194C>ACA406038579ATP1A3c.2572G>T (p.Gly858Trp)
c.2533G>T (p.Gly845Trp)
c.2566G>T (p.Gly856Trp)
c.2443G>T (p.Gly815Trp)
19g.41970194C=CA2336721083ATP1A3c.2572G= (p.Gly858=)
c.2533G= (p.Gly845=)
c.2566G= (p.Gly856=)
c.2443G= (p.Gly815=)
19g.41970194C>GCA406038580ATP1A3c.2572G>C (p.Gly858Arg)
c.2533G>C (p.Gly845Arg)
c.2566G>C (p.Gly856Arg)
c.2443G>C (p.Gly815Arg)
19g.41970194C>TCA406038574ATP1A3c.2572G>A (p.Gly858Arg)
c.2533G>A (p.Gly845Arg)
c.2566G>A (p.Gly856Arg)
c.2443G>A (p.Gly815Arg)
ClinVar dbSNP gnomAD v4 COSMIC
19g.41970195G>ACA9467367ATP1A3c.2571C>T (p.Tyr857=)
c.2532C>T (p.Tyr844=)
c.2565C>T (p.Tyr855=)
c.2442C>T (p.Tyr814=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41970195G>CCA406038581ATP1A3c.2571C>G (p.Tyr857Ter)
c.2532C>G (p.Tyr844Ter)
c.2565C>G (p.Tyr855Ter)
c.2442C>G (p.Tyr814Ter)
19g.41970195G=CA2336721084ATP1A3c.2571C= (p.Tyr857=)
c.2532C= (p.Tyr844=)
c.2565C= (p.Tyr855=)
c.2442C= (p.Tyr814=)
19g.41970195G>TCA406038583ATP1A3c.2571C>A (p.Tyr857Ter)
c.2532C>A (p.Tyr844Ter)
c.2565C>A (p.Tyr855Ter)
c.2442C>A (p.Tyr814Ter)
19g.41970196T>ACA406038586ATP1A3c.2570A>T (p.Tyr857Phe)
c.2531A>T (p.Tyr844Phe)
c.2564A>T (p.Tyr855Phe)
c.2441A>T (p.Tyr814Phe)
19g.41970196T>CCA406038587ATP1A3c.2570A>G (p.Tyr857Cys)
c.2531A>G (p.Tyr844Cys)
c.2564A>G (p.Tyr855Cys)
c.2441A>G (p.Tyr814Cys)
ClinVar
19g.41970196T>GCA406038589ATP1A3c.2570A>C (p.Tyr857Ser)
c.2531A>C (p.Tyr844Ser)
c.2564A>C (p.Tyr855Ser)
c.2441A>C (p.Tyr814Ser)
19g.41970197A>CCA406038590ATP1A3c.2569T>G (p.Tyr857Asp)
c.2530T>G (p.Tyr844Asp)
c.2563T>G (p.Tyr855Asp)
c.2440T>G (p.Tyr814Asp)
19g.41970197A>GCA406038593ATP1A3c.2569T>C (p.Tyr857His)
c.2530T>C (p.Tyr844His)
c.2563T>C (p.Tyr855His)
c.2440T>C (p.Tyr814His)
19g.41970197A>TCA406038591ATP1A3c.2569T>A (p.Tyr857Asn)
c.2530T>A (p.Tyr844Asn)
c.2563T>A (p.Tyr855Asn)
c.2440T>A (p.Tyr814Asn)
19g.41970197_41970198delinsAGCA2336721085ATP1A3c.2568_2569delinsCT (p.Ala856=)
c.2529_2530delinsCT (p.Ala843=)
c.2562_2563delinsCT (p.Ala854=)
c.2439_2440delinsCT (p.Ala813=)
19g.41970198G>ACA507694617ATP1A3c.2568C>T (p.Ala856=)
c.2529C>T (p.Ala843=)
c.2562C>T (p.Ala854=)
c.2439C>T (p.Ala813=)
gnomAD v4
19g.41970198G>CCA507694618ATP1A3c.2568C>G (p.Ala856=)
c.2529C>G (p.Ala843=)
c.2562C>G (p.Ala854=)
c.2439C>G (p.Ala813=)
gnomAD v4
19g.41970198G>TCA507694619ATP1A3c.2568C>A (p.Ala856=)
c.2529C>A (p.Ala843=)
c.2562C>A (p.Ala854=)
c.2439C>A (p.Ala813=)
19g.41970199delCA308586368ATP1A3c.2568del (p.Tyr857ThrfsTer6)
c.2529del (p.Tyr844ThrfsTer6)
c.2562del (p.Tyr855ThrfsTer6)
c.2439del (p.Tyr814ThrfsTer6)
dbSNP
19g.41970199G>ACA406038595ATP1A3c.2567C>T (p.Ala856Val)
c.2528C>T (p.Ala843Val)
c.2561C>T (p.Ala854Val)
c.2438C>T (p.Ala813Val)
gnomAD v4
19g.41970199G>CCA406038597ATP1A3c.2567C>G (p.Ala856Gly)
c.2528C>G (p.Ala843Gly)
c.2561C>G (p.Ala854Gly)
c.2438C>G (p.Ala813Gly)
19g.41970199G>TCA406038598ATP1A3c.2567C>A (p.Ala856Asp)
c.2528C>A (p.Ala843Asp)
c.2561C>A (p.Ala854Asp)
c.2438C>A (p.Ala813Asp)
ClinVar
19g.41970200C>ACA406038600ATP1A3c.2566G>T (p.Ala856Ser)
c.2527G>T (p.Ala843Ser)
c.2560G>T (p.Ala854Ser)
c.2437G>T (p.Ala813Ser)
19g.41970200C>GCA406038604ATP1A3c.2566G>C (p.Ala856Pro)
c.2527G>C (p.Ala843Pro)
c.2560G>C (p.Ala854Pro)
c.2437G>C (p.Ala813Pro)
19g.41970200C>TCA406038603ATP1A3c.2566G>A (p.Ala856Thr)
c.2527G>A (p.Ala843Thr)
c.2560G>A (p.Ala854Thr)
c.2437G>A (p.Ala813Thr)
19g.41970201C>ACA406038605ATP1A3c.2565G>T (p.Met855Ile)
c.2526G>T (p.Met842Ile)
c.2559G>T (p.Met853Ile)
c.2436G>T (p.Met812Ile)
19g.41970201C>GCA406038607ATP1A3c.2565G>C (p.Met855Ile)
c.2526G>C (p.Met842Ile)
c.2559G>C (p.Met853Ile)
c.2436G>C (p.Met812Ile)
19g.41970201C>TCA406038609ATP1A3c.2565G>A (p.Met855Ile)
c.2526G>A (p.Met842Ile)
c.2559G>A (p.Met853Ile)
c.2436G>A (p.Met812Ile)
19g.41970202A>CCA406038611ATP1A3c.2564T>G (p.Met855Arg)
c.2525T>G (p.Met842Arg)
c.2558T>G (p.Met853Arg)
c.2435T>G (p.Met812Arg)
19g.41970202A>GCA406038613ATP1A3c.2564T>C (p.Met855Thr)
c.2525T>C (p.Met842Thr)
c.2558T>C (p.Met853Thr)
c.2435T>C (p.Met812Thr)
ClinVar
19g.41970202A>TCA406038615ATP1A3c.2564T>A (p.Met855Lys)
c.2525T>A (p.Met842Lys)
c.2558T>A (p.Met853Lys)
c.2435T>A (p.Met812Lys)
19g.41970203T>ACA406038618ATP1A3c.2563A>T (p.Met855Leu)
c.2524A>T (p.Met842Leu)
c.2557A>T (p.Met853Leu)
c.2434A>T (p.Met812Leu)
19g.41970203T>CCA406038620ATP1A3c.2563A>G (p.Met855Val)
c.2524A>G (p.Met842Val)
c.2557A>G (p.Met853Val)
c.2434A>G (p.Met812Val)
19g.41970203T>GCA406038622ATP1A3c.2563A>C (p.Met855Leu)
c.2524A>C (p.Met842Leu)
c.2557A>C (p.Met853Leu)
c.2434A>C (p.Met812Leu)
19g.41970204G>ACA507694621ATP1A3c.2562C>T (p.Ser854=)
c.2523C>T (p.Ser841=)
c.2556C>T (p.Ser852=)
c.2433C>T (p.Ser811=)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.41970204G>CCA406038624ATP1A3c.2562C>G (p.Ser854Arg)
c.2523C>G (p.Ser841Arg)
c.2556C>G (p.Ser852Arg)
c.2433C>G (p.Ser811Arg)
19g.41970204G=CA2336721087ATP1A3c.2562C= (p.Ser854=)
c.2523C= (p.Ser841=)
c.2556C= (p.Ser852=)
c.2433C= (p.Ser811=)
19g.41970204G>TCA406038625ATP1A3c.2562C>A (p.Ser854Arg)
c.2523C>A (p.Ser841Arg)
c.2556C>A (p.Ser852Arg)
c.2433C>A (p.Ser811Arg)
19g.41970205C>ACA406038629ATP1A3c.2561G>T (p.Ser854Ile)
c.2522G>T (p.Ser841Ile)
c.2555G>T (p.Ser852Ile)
c.2432G>T (p.Ser811Ile)
19g.41970205C>GCA406038631ATP1A3c.2561G>C (p.Ser854Thr)
c.2522G>C (p.Ser841Thr)
c.2555G>C (p.Ser852Thr)
c.2432G>C (p.Ser811Thr)
19g.41970205C>TCA406038627ATP1A3c.2561G>A (p.Ser854Asn)
c.2522G>A (p.Ser841Asn)
c.2555G>A (p.Ser852Asn)
c.2432G>A (p.Ser811Asn)
19g.41970206T>ACA406038633ATP1A3c.2560A>T (p.Ser854Cys)
c.2521A>T (p.Ser841Cys)
c.2554A>T (p.Ser852Cys)
c.2431A>T (p.Ser811Cys)
19g.41970206T>CCA406038634ATP1A3c.2560A>G (p.Ser854Gly)
c.2521A>G (p.Ser841Gly)
c.2554A>G (p.Ser852Gly)
c.2431A>G (p.Ser811Gly)
19g.41970206T>GCA406038636ATP1A3c.2560A>C (p.Ser854Arg)
c.2521A>C (p.Ser841Arg)
c.2554A>C (p.Ser852Arg)
c.2431A>C (p.Ser811Arg)
19g.41970207G>ACA507694622ATP1A3c.2559C>T (p.Ile853=)
c.2520C>T (p.Ile840=)
c.2553C>T (p.Ile851=)
c.2430C>T (p.Ile810=)
19g.41970207G>CCA406038638ATP1A3c.2559C>G (p.Ile853Met)
c.2520C>G (p.Ile840Met)
c.2553C>G (p.Ile851Met)
c.2430C>G (p.Ile810Met)
19g.41970207G>TCA507694623ATP1A3c.2559C>A (p.Ile853=)
c.2520C>A (p.Ile840=)
c.2553C>A (p.Ile851=)
c.2430C>A (p.Ile810=)
gnomAD v4
19g.41970208A>CCA406038640ATP1A3c.2558T>G (p.Ile853Ser)
c.2519T>G (p.Ile840Ser)
c.2552T>G (p.Ile851Ser)
c.2429T>G (p.Ile810Ser)
19g.41970208A>GCA406038641ATP1A3c.2558T>C (p.Ile853Thr)
c.2519T>C (p.Ile840Thr)
c.2552T>C (p.Ile851Thr)
c.2429T>C (p.Ile810Thr)
gnomAD v4
19g.41970208A>TCA406038642ATP1A3c.2558T>A (p.Ile853Asn)
c.2519T>A (p.Ile840Asn)
c.2552T>A (p.Ile851Asn)
c.2429T>A (p.Ile810Asn)
19g.41970209T>ACA406038644ATP1A3c.2557A>T (p.Ile853Phe)
c.2518A>T (p.Ile840Phe)
c.2551A>T (p.Ile851Phe)
c.2428A>T (p.Ile810Phe)
19g.41970209T>CCA406038648ATP1A3c.2557A>G (p.Ile853Val)
c.2518A>G (p.Ile840Val)
c.2551A>G (p.Ile851Val)
c.2428A>G (p.Ile810Val)
19g.41970209T>GCA406038646ATP1A3c.2557A>C (p.Ile853Leu)
c.2518A>C (p.Ile840Leu)
c.2551A>C (p.Ile851Leu)
c.2428A>C (p.Ile810Leu)
19g.41970210G>ACA507694624ATP1A3c.2556C>T (p.Leu852=)
c.2517C>T (p.Leu839=)
c.2550C>T (p.Leu850=)
c.2427C>T (p.Leu809=)
19g.41970210G>CCA507694625ATP1A3c.2556C>G (p.Leu852=)
c.2517C>G (p.Leu839=)
c.2550C>G (p.Leu850=)
c.2427C>G (p.Leu809=)
COSMIC
19g.41970210G>TCA507694626ATP1A3c.2556C>A (p.Leu852=)
c.2517C>A (p.Leu839=)
c.2550C>A (p.Leu850=)
c.2427C>A (p.Leu809=)
19g.41970210_41970215delinsGAGTCTCA2336721089ATP1A3c.2551_2556delinsAGACTC (p.Arg851=)
c.2512_2517delinsAGACTC (p.Arg838=)
c.2545_2550delinsAGACTC (p.Arg849=)
c.2422_2427delinsAGACTC (p.Arg808=)
19g.41970211A>CCA406038650ATP1A3c.2555T>G (p.Leu852Arg)
c.2516T>G (p.Leu839Arg)
c.2549T>G (p.Leu850Arg)
c.2426T>G (p.Leu809Arg)
19g.41970211A>GCA406038653ATP1A3c.2555T>C (p.Leu852Pro)
c.2516T>C (p.Leu839Pro)
c.2549T>C (p.Leu850Pro)
c.2426T>C (p.Leu809Pro)
19g.41970211A>TCA406038655ATP1A3c.2555T>A (p.Leu852His)
c.2516T>A (p.Leu839His)
c.2549T>A (p.Leu850His)
c.2426T>A (p.Leu809His)
19g.41970211_41970215delinsGACA10654769ATP1A3c.2551_2555delinsTC (p.Arg851_Leu852delinsSer)
c.2512_2516delinsTC (p.Arg838_Leu839delinsSer)
c.2545_2549delinsTC (p.Arg849_Leu850delinsSer)
c.2422_2426delinsTC (p.Arg808_Leu809delinsSer)
ClinVar dbSNP
19g.41970212G>ACA406038656ATP1A3c.2554C>T (p.Leu852Phe)
c.2515C>T (p.Leu839Phe)
c.2548C>T (p.Leu850Phe)
c.2425C>T (p.Leu809Phe)
19g.41970212G>CCA406038658ATP1A3c.2554C>G (p.Leu852Val)
c.2515C>G (p.Leu839Val)
c.2548C>G (p.Leu850Val)
c.2425C>G (p.Leu809Val)
19g.41970212G>TCA406038657ATP1A3c.2554C>A (p.Leu852Ile)
c.2515C>A (p.Leu839Ile)
c.2548C>A (p.Leu850Ile)
c.2425C>A (p.Leu809Ile)
19g.41970213T>ACA406038660ATP1A3c.2553A>T (p.Arg851Ser)
c.2514A>T (p.Arg838Ser)
c.2547A>T (p.Arg849Ser)
c.2424A>T (p.Arg808Ser)
19g.41970213T>CCA507694628ATP1A3c.2553A>G (p.Arg851=)
c.2514A>G (p.Arg838=)
c.2547A>G (p.Arg849=)
c.2424A>G (p.Arg808=)
ClinVar
19g.41970213T>GCA406038662ATP1A3c.2553A>C (p.Arg851Ser)
c.2514A>C (p.Arg838Ser)
c.2547A>C (p.Arg849Ser)
c.2424A>C (p.Arg808Ser)
19g.41970214C>ACA406038664ATP1A3c.2552G>T (p.Arg851Ile)
c.2513G>T (p.Arg838Ile)
c.2546G>T (p.Arg849Ile)
c.2423G>T (p.Arg808Ile)
19g.41970214C>GCA406038666ATP1A3c.2552G>C (p.Arg851Thr)
c.2513G>C (p.Arg838Thr)
c.2546G>C (p.Arg849Thr)
c.2423G>C (p.Arg808Thr)
19g.41970214C>TCA406038668ATP1A3c.2552G>A (p.Arg851Lys)
c.2513G>A (p.Arg838Lys)
c.2546G>A (p.Arg849Lys)
c.2423G>A (p.Arg808Lys)
19g.41970215T>ACA406038670ATP1A3c.2551A>T (p.Arg851Ter)
c.2512A>T (p.Arg838Ter)
c.2545A>T (p.Arg849Ter)
c.2422A>T (p.Arg808Ter)
19g.41970215T>CCA406038672ATP1A3c.2551A>G (p.Arg851Gly)
c.2512A>G (p.Arg838Gly)
c.2545A>G (p.Arg849Gly)
c.2422A>G (p.Arg808Gly)
19g.41970215T>GCA507694630ATP1A3c.2551A>C (p.Arg851=)
c.2512A>C (p.Arg838=)
c.2545A>C (p.Arg849=)
c.2422A>C (p.Arg808=)
19g.41970216C>ACA406038674ATP1A3c.2550G>T (p.Glu850Asp)
c.2511G>T (p.Glu837Asp)
c.2544G>T (p.Glu848Asp)
c.2421G>T (p.Glu807Asp)
19g.41970216C>GCA406038676ATP1A3c.2550G>C (p.Glu850Asp)
c.2511G>C (p.Glu837Asp)
c.2544G>C (p.Glu848Asp)
c.2421G>C (p.Glu807Asp)
19g.41970216C>TCA507694631ATP1A3c.2550G>A (p.Glu850=)
c.2511G>A (p.Glu837=)
c.2544G>A (p.Glu848=)
c.2421G>A (p.Glu807=)
gnomAD v4
19g.41970217T>ACA406038678ATP1A3c.2549A>T (p.Glu850Val)
c.2510A>T (p.Glu837Val)
c.2543A>T (p.Glu848Val)
c.2420A>T (p.Glu807Val)
19g.41970217T>CCA406038679ATP1A3c.2549A>G (p.Glu850Gly)
c.2510A>G (p.Glu837Gly)
c.2543A>G (p.Glu848Gly)
c.2420A>G (p.Glu807Gly)
19g.41970217T>GCA406038680ATP1A3c.2549A>C (p.Glu850Ala)
c.2510A>C (p.Glu837Ala)
c.2543A>C (p.Glu848Ala)
c.2420A>C (p.Glu807Ala)
19g.41970218C>ACA406038683ATP1A3c.2548G>T (p.Glu850Ter)
c.2509G>T (p.Glu837Ter)
c.2542G>T (p.Glu848Ter)
c.2419G>T (p.Glu807Ter)
19g.41970218C=CA2336721116ATP1A3c.2548G= (p.Glu850=)
c.2509G= (p.Glu837=)
c.2542G= (p.Glu848=)
c.2419G= (p.Glu807=)
19g.41970218C>GCA406038686ATP1A3c.2548G>C (p.Glu850Gln)
c.2509G>C (p.Glu837Gln)
c.2542G>C (p.Glu848Gln)
c.2419G>C (p.Glu807Gln)
19g.41970218C>TCA406038684ATP1A3c.2548G>A (p.Glu850Lys)
c.2509G>A (p.Glu837Lys)
c.2542G>A (p.Glu848Lys)
c.2419G>A (p.Glu807Lys)
ClinVar dbSNP gnomAD v4
19g.41970219A>CCA406038687ATP1A3c.2547T>G (p.Asn849Lys)
c.2508T>G (p.Asn836Lys)
c.2541T>G (p.Asn847Lys)
c.2418T>G (p.Asn806Lys)
19g.41970219A>GCA507694632ATP1A3c.2547T>C (p.Asn849=)
c.2508T>C (p.Asn836=)
c.2541T>C (p.Asn847=)
c.2418T>C (p.Asn806=)
19g.41970219A>TCA406038689ATP1A3c.2547T>A (p.Asn849Lys)
c.2508T>A (p.Asn836Lys)
c.2541T>A (p.Asn847Lys)
c.2418T>A (p.Asn806Lys)
19g.41970220T>ACA406038691ATP1A3c.2546A>T (p.Asn849Ile)
c.2507A>T (p.Asn836Ile)
c.2540A>T (p.Asn847Ile)
c.2417A>T (p.Asn806Ile)
19g.41970220T>CCA406038693ATP1A3c.2546A>G (p.Asn849Ser)
c.2507A>G (p.Asn836Ser)
c.2540A>G (p.Asn847Ser)
c.2417A>G (p.Asn806Ser)
19g.41970220T>GCA406038695ATP1A3c.2546A>C (p.Asn849Thr)
c.2507A>C (p.Asn836Thr)
c.2540A>C (p.Asn847Thr)
c.2417A>C (p.Asn806Thr)
19g.41970221T>ACA406038697ATP1A3c.2545A>T (p.Asn849Tyr)
c.2506A>T (p.Asn836Tyr)
c.2539A>T (p.Asn847Tyr)
c.2416A>T (p.Asn806Tyr)
19g.41970221T>CCA406038699ATP1A3c.2545A>G (p.Asn849Asp)
c.2506A>G (p.Asn836Asp)
c.2539A>G (p.Asn847Asp)
c.2416A>G (p.Asn806Asp)
19g.41970221T>GCA406038701ATP1A3c.2545A>C (p.Asn849His)
c.2506A>C (p.Asn836His)
c.2539A>C (p.Asn847His)
c.2416A>C (p.Asn806His)
19g.41970222G>ACA507694633ATP1A3c.2544C>T (p.Val848=)
c.2505C>T (p.Val835=)
c.2538C>T (p.Val846=)
c.2415C>T (p.Val805=)
19g.41970222G>CCA507694634ATP1A3c.2544C>G (p.Val848=)
c.2505C>G (p.Val835=)
c.2538C>G (p.Val846=)
c.2415C>G (p.Val805=)
19g.41970222G>TCA507694635ATP1A3c.2544C>A (p.Val848=)
c.2505C>A (p.Val835=)
c.2538C>A (p.Val846=)
c.2415C>A (p.Val805=)
19g.41970223A>CCA406038703ATP1A3c.2543T>G (p.Val848Gly)
c.2504T>G (p.Val835Gly)
c.2537T>G (p.Val846Gly)
c.2414T>G (p.Val805Gly)
19g.41970223A>GCA406038705ATP1A3c.2543T>C (p.Val848Ala)
c.2504T>C (p.Val835Ala)
c.2537T>C (p.Val846Ala)
c.2414T>C (p.Val805Ala)
19g.41970223A>TCA406038706ATP1A3c.2543T>A (p.Val848Asp)
c.2504T>A (p.Val835Asp)
c.2537T>A (p.Val846Asp)
c.2414T>A (p.Val805Asp)
19g.41970224C>ACA406038709ATP1A3c.2542G>T (p.Val848Phe)
c.2503G>T (p.Val835Phe)
c.2536G>T (p.Val846Phe)
c.2413G>T (p.Val805Phe)
19g.41970224C>GCA406038708ATP1A3c.2542G>C (p.Val848Leu)
c.2503G>C (p.Val835Leu)
c.2536G>C (p.Val846Leu)
c.2413G>C (p.Val805Leu)
19g.41970224C>TCA406038707ATP1A3c.2542G>A (p.Val848Ile)
c.2503G>A (p.Val835Ile)
c.2536G>A (p.Val846Ile)
c.2413G>A (p.Val805Ile)
19g.41970225C>ACA406038710ATP1A3c.2541G>T (p.Leu847Phe)
c.2502G>T (p.Leu834Phe)
c.2535G>T (p.Leu845Phe)
c.2412G>T (p.Leu804Phe)
19g.41970225C=CA2336721119ATP1A3c.2541G= (p.Leu847=)
c.2502G= (p.Leu834=)
c.2535G= (p.Leu845=)
c.2412G= (p.Leu804=)
19g.41970225C>GCA406038711ATP1A3c.2541G>C (p.Leu847Phe)
c.2502G>C (p.Leu834Phe)
c.2535G>C (p.Leu845Phe)
c.2412G>C (p.Leu804Phe)
19g.41970225C>TCA507694691ATP1A3c.2541G>A (p.Leu847=)
c.2502G>A (p.Leu834=)
c.2535G>A (p.Leu845=)
c.2412G>A (p.Leu804=)
dbSNP
19g.41970226A>CCA406038712ATP1A3c.2540T>G (p.Leu847Trp)
c.2501T>G (p.Leu834Trp)
c.2534T>G (p.Leu845Trp)
c.2411T>G (p.Leu804Trp)
19g.41970226A>GCA406038713ATP1A3c.2540T>C (p.Leu847Ser)
c.2501T>C (p.Leu834Ser)
c.2534T>C (p.Leu845Ser)
c.2411T>C (p.Leu804Ser)
19g.41970226A>TCA406038714ATP1A3c.2540T>A (p.Leu847Ter)
c.2501T>A (p.Leu834Ter)
c.2534T>A (p.Leu845Ter)
c.2411T>A (p.Leu804Ter)
19g.41970227A=CA2336721121ATP1A3c.2539T= (p.Leu847=)
c.2500T= (p.Leu834=)
c.2533T= (p.Leu845=)
c.2410T= (p.Leu804=)
19g.41970227A>CCA406038715ATP1A3c.2539T>G (p.Leu847Val)
c.2500T>G (p.Leu834Val)
c.2533T>G (p.Leu845Val)
c.2410T>G (p.Leu804Val)
19g.41970227A>GCA9467368ATP1A3c.2539T>C (p.Leu847=)
c.2500T>C (p.Leu834=)
c.2533T>C (p.Leu845=)
c.2410T>C (p.Leu804=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41970227A>TCA406038716ATP1A3c.2539T>A (p.Leu847Met)
c.2500T>A (p.Leu834Met)
c.2533T>A (p.Leu845Met)
c.2410T>A (p.Leu804Met)
19g.41970228T>ACA406038717ATP1A3c.2538A>T (p.Lys846Asn)
c.2499A>T (p.Lys833Asn)
c.2532A>T (p.Lys844Asn)
c.2409A>T (p.Lys803Asn)
19g.41970228T>CCA507694695ATP1A3c.2538A>G (p.Lys846=)
c.2499A>G (p.Lys833=)
c.2532A>G (p.Lys844=)
c.2409A>G (p.Lys803=)
19g.41970228T>GCA406038718ATP1A3c.2538A>C (p.Lys846Asn)
c.2499A>C (p.Lys833Asn)
c.2532A>C (p.Lys844Asn)
c.2409A>C (p.Lys803Asn)
19g.41970229T>ACA406038719ATP1A3c.2537A>T (p.Lys846Ile)
c.2498A>T (p.Lys833Ile)
c.2531A>T (p.Lys844Ile)
c.2408A>T (p.Lys803Ile)
19g.41970229T>CCA406038720ATP1A3c.2537A>G (p.Lys846Arg)
c.2498A>G (p.Lys833Arg)
c.2531A>G (p.Lys844Arg)
c.2408A>G (p.Lys803Arg)
19g.41970229T>GCA406038722ATP1A3c.2537A>C (p.Lys846Thr)
c.2498A>C (p.Lys833Thr)
c.2531A>C (p.Lys844Thr)
c.2408A>C (p.Lys803Thr)
19g.41970230T>ACA406038726ATP1A3c.2536A>T (p.Lys846Ter)
c.2497A>T (p.Lys833Ter)
c.2530A>T (p.Lys844Ter)
c.2407A>T (p.Lys803Ter)
19g.41970230T>CCA406038727ATP1A3c.2536A>G (p.Lys846Glu)
c.2497A>G (p.Lys833Glu)
c.2530A>G (p.Lys844Glu)
c.2407A>G (p.Lys803Glu)
19g.41970230T>GCA406038724ATP1A3c.2536A>C (p.Lys846Gln)
c.2497A>C (p.Lys833Gln)
c.2530A>C (p.Lys844Gln)
c.2407A>C (p.Lys803Gln)
19g.41970231G>ACA507694697ATP1A3c.2535C>T (p.Asp845=)
c.2496C>T (p.Asp832=)
c.2529C>T (p.Asp843=)
c.2406C>T (p.Asp802=)
ClinVar
19g.41970231G>CCA406038731ATP1A3c.2535C>G (p.Asp845Glu)
c.2496C>G (p.Asp832Glu)
c.2529C>G (p.Asp843Glu)
c.2406C>G (p.Asp802Glu)
19g.41970231G>TCA406038730ATP1A3c.2535C>A (p.Asp845Glu)
c.2496C>A (p.Asp832Glu)
c.2529C>A (p.Asp843Glu)
c.2406C>A (p.Asp802Glu)
19g.41970232T>ACA406038733ATP1A3c.2534A>T (p.Asp845Val)
c.2495A>T (p.Asp832Val)
c.2528A>T (p.Asp843Val)
c.2405A>T (p.Asp802Val)
19g.41970232T>CCA406038735ATP1A3c.2534A>G (p.Asp845Gly)
c.2495A>G (p.Asp832Gly)
c.2528A>G (p.Asp843Gly)
c.2405A>G (p.Asp802Gly)
19g.41970232T>GCA406038737ATP1A3c.2534A>C (p.Asp845Ala)
c.2495A>C (p.Asp832Ala)
c.2528A>C (p.Asp843Ala)
c.2405A>C (p.Asp802Ala)
19g.41970233C>ACA406038739ATP1A3c.2533G>T (p.Asp845Tyr)
c.2494G>T (p.Asp832Tyr)
c.2527G>T (p.Asp843Tyr)
c.2404G>T (p.Asp802Tyr)
19g.41970233C>GCA406038741ATP1A3c.2533G>C (p.Asp845His)
c.2494G>C (p.Asp832His)
c.2527G>C (p.Asp843His)
c.2404G>C (p.Asp802His)
19g.41970233C>TCA406038744ATP1A3c.2533G>A (p.Asp845Asn)
c.2494G>A (p.Asp832Asn)
c.2527G>A (p.Asp843Asn)
c.2404G>A (p.Asp802Asn)
COSMIC
19g.41970234C>ACA507694701ATP1A3c.2532G>T (p.Thr844=)
c.2493G>T (p.Thr831=)
c.2526G>T (p.Thr842=)
c.2403G>T (p.Thr801=)
19g.41970234C=CA2336721132ATP1A3c.2532G= (p.Thr844=)
c.2493G= (p.Thr831=)
c.2526G= (p.Thr842=)
c.2403G= (p.Thr801=)
19g.41970234C>GCA9467369ATP1A3c.2532G>C (p.Thr844=)
c.2493G>C (p.Thr831=)
c.2526G>C (p.Thr842=)
c.2403G>C (p.Thr801=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41970234C>TCA9467370ATP1A3c.2532G>A (p.Thr844=)
c.2493G>A (p.Thr831=)
c.2526G>A (p.Thr842=)
c.2403G>A (p.Thr801=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41970235G>ACA9467371ATP1A3c.2531C>T (p.Thr844Met)
c.2492C>T (p.Thr831Met)
c.2525C>T (p.Thr842Met)
c.2402C>T (p.Thr801Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
19g.41970235G>CCA406038749ATP1A3c.2531C>G (p.Thr844Arg)
c.2492C>G (p.Thr831Arg)
c.2525C>G (p.Thr842Arg)
c.2402C>G (p.Thr801Arg)
19g.41970235G=CA2336721139ATP1A3c.2531C= (p.Thr844=)
c.2492C= (p.Thr831=)
c.2525C= (p.Thr842=)
c.2402C= (p.Thr801=)
19g.41970235G>TCA406038751ATP1A3c.2531C>A (p.Thr844Lys)
c.2492C>A (p.Thr831Lys)
c.2525C>A (p.Thr842Lys)
c.2402C>A (p.Thr801Lys)
19g.41970236T>ACA406038752ATP1A3c.2530A>T (p.Thr844Ser)
c.2491A>T (p.Thr831Ser)
c.2524A>T (p.Thr842Ser)
c.2401A>T (p.Thr801Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.41970236T>CCA406038754ATP1A3c.2530A>G (p.Thr844Ala)
c.2491A>G (p.Thr831Ala)
c.2524A>G (p.Thr842Ala)
c.2401A>G (p.Thr801Ala)
19g.41970236T>GCA406038756ATP1A3c.2530A>C (p.Thr844Pro)
c.2491A>C (p.Thr831Pro)
c.2524A>C (p.Thr842Pro)
c.2401A>C (p.Thr801Pro)
19g.41970236T=CA2336721142ATP1A3c.2530A= (p.Thr844=)
c.2491A= (p.Thr831=)
c.2524A= (p.Thr842=)
c.2401A= (p.Thr801=)
19g.41970237C>ACA507694706ATP1A3c.2529G>T (p.Arg843=)
c.2490G>T (p.Arg830=)
c.2523G>T (p.Arg841=)
c.2400G>T (p.Arg800=)
19g.41970237C>GCA507694707ATP1A3c.2529G>C (p.Arg843=)
c.2490G>C (p.Arg830=)
c.2523G>C (p.Arg841=)
c.2400G>C (p.Arg800=)
19g.41970237C>TCA507694705ATP1A3c.2529G>A (p.Arg843=)
c.2490G>A (p.Arg830=)
c.2523G>A (p.Arg841=)
c.2400G>A (p.Arg800=)
19g.41970238C>ACA406038758ATP1A3c.2528G>T (p.Arg843Leu)
c.2489G>T (p.Arg830Leu)
c.2522G>T (p.Arg841Leu)
c.2399G>T (p.Arg800Leu)
19g.41970238C=CA2336721149ATP1A3c.2528G= (p.Arg843=)
c.2489G= (p.Arg830=)
c.2522G= (p.Arg841=)
c.2399G= (p.Arg800=)
19g.41970238C>GCA406038762ATP1A3c.2528G>C (p.Arg843Pro)
c.2489G>C (p.Arg830Pro)
c.2522G>C (p.Arg841Pro)
c.2399G>C (p.Arg800Pro)
19g.41970238C>TCA9467372ATP1A3c.2528G>A (p.Arg843Gln)
c.2489G>A (p.Arg830Gln)
c.2522G>A (p.Arg841Gln)
c.2399G>A (p.Arg800Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.41970239G>ACA406038764ATP1A3c.2527C>T (p.Arg843Trp)
c.2488C>T (p.Arg830Trp)
c.2521C>T (p.Arg841Trp)
c.2398C>T (p.Arg800Trp)
gnomAD v4
19g.41970239G>CCA9467373ATP1A3c.2527C>G (p.Arg843Gly)
c.2488C>G (p.Arg830Gly)
c.2521C>G (p.Arg841Gly)
c.2398C>G (p.Arg800Gly)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.41970239G=CA2336721151ATP1A3c.2527C= (p.Arg843=)
c.2488C= (p.Arg830=)
c.2521C= (p.Arg841=)
c.2398C= (p.Arg800=)
19g.41970239G>TCA507694708ATP1A3c.2527C>A (p.Arg843=)
c.2488C>A (p.Arg830=)
c.2521C>A (p.Arg841=)
c.2398C>A (p.Arg800=)
ClinVar dbSNP gnomAD v4
19g.41970240C>ACA507694710ATP1A3c.2526G>T (p.Pro842=)
c.2487G>T (p.Pro829=)
c.2520G>T (p.Pro840=)
c.2397G>T (p.Pro799=)
19g.41970240C=CA2336721154ATP1A3c.2526G= (p.Pro842=)
c.2487G= (p.Pro829=)
c.2520G= (p.Pro840=)
c.2397G= (p.Pro799=)
19g.41970240C>GCA507694709ATP1A3c.2526G>C (p.Pro842=)
c.2487G>C (p.Pro829=)
c.2520G>C (p.Pro840=)
c.2397G>C (p.Pro799=)
19g.41970240C>TCA9467374ATP1A3c.2526G>A (p.Pro842=)
c.2487G>A (p.Pro829=)
c.2520G>A (p.Pro840=)
c.2397G>A (p.Pro799=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41970241G>ACA406038768ATP1A3c.2525C>T (p.Pro842Leu)
c.2486C>T (p.Pro829Leu)
c.2519C>T (p.Pro840Leu)
c.2396C>T (p.Pro799Leu)
ClinVar dbSNP gnomAD v4 COSMIC
19g.41970241G>CCA406038769ATP1A3c.2525C>G (p.Pro842Arg)
c.2486C>G (p.Pro829Arg)
c.2519C>G (p.Pro840Arg)
c.2396C>G (p.Pro799Arg)
19g.41970241G>TCA406038771ATP1A3c.2525C>A (p.Pro842Gln)
c.2486C>A (p.Pro829Gln)
c.2519C>A (p.Pro840Gln)
c.2396C>A (p.Pro799Gln)
19g.41970242G>ACA406038774ATP1A3c.2524C>T (p.Pro842Ser)
c.2485C>T (p.Pro829Ser)
c.2518C>T (p.Pro840Ser)
c.2395C>T (p.Pro799Ser)
19g.41970242G>CCA406038775ATP1A3c.2524C>G (p.Pro842Ala)
c.2485C>G (p.Pro829Ala)
c.2518C>G (p.Pro840Ala)
c.2395C>G (p.Pro799Ala)
19g.41970242G>TCA406038777ATP1A3c.2524C>A (p.Pro842Thr)
c.2485C>A (p.Pro829Thr)
c.2518C>A (p.Pro840Thr)
c.2395C>A (p.Pro799Thr)
19g.41970243G>ACA507694712ATP1A3c.2523C>T (p.Asn841=)
c.2484C>T (p.Asn828=)
c.2517C>T (p.Asn839=)
c.2394C>T (p.Asn798=)
19g.41970243G>CCA406038779ATP1A3c.2523C>G (p.Asn841Lys)
c.2484C>G (p.Asn828Lys)
c.2517C>G (p.Asn839Lys)
c.2394C>G (p.Asn798Lys)
19g.41970243G>TCA406038781ATP1A3c.2523C>A (p.Asn841Lys)
c.2484C>A (p.Asn828Lys)
c.2517C>A (p.Asn839Lys)
c.2394C>A (p.Asn798Lys)
19g.41970244T>ACA406038784ATP1A3c.2522A>T (p.Asn841Ile)
c.2483A>T (p.Asn828Ile)
c.2516A>T (p.Asn839Ile)
c.2393A>T (p.Asn798Ile)
19g.41970244T>CCA406038787ATP1A3c.2522A>G (p.Asn841Ser)
c.2483A>G (p.Asn828Ser)
c.2516A>G (p.Asn839Ser)
c.2393A>G (p.Asn798Ser)
19g.41970244T>GCA406038786ATP1A3c.2522A>C (p.Asn841Thr)
c.2483A>C (p.Asn828Thr)
c.2516A>C (p.Asn839Thr)
c.2393A>C (p.Asn798Thr)
ClinVar
19g.41970245T>ACA406038790ATP1A3c.2521A>T (p.Asn841Tyr)
c.2482A>T (p.Asn828Tyr)
c.2515A>T (p.Asn839Tyr)
c.2392A>T (p.Asn798Tyr)
19g.41970245T>CCA406038791ATP1A3c.2521A>G (p.Asn841Asp)
c.2482A>G (p.Asn828Asp)
c.2515A>G (p.Asn839Asp)
c.2392A>G (p.Asn798Asp)
19g.41970245T>GCA406038793ATP1A3c.2521A>C (p.Asn841His)
c.2482A>C (p.Asn828His)
c.2515A>C (p.Asn839His)
c.2392A>C (p.Asn798His)
19g.41970246C>ACA406038794ATP1A3c.2520G>T (p.Arg840Ser)
c.2481G>T (p.Arg827Ser)
c.2514G>T (p.Arg838Ser)
c.2391G>T (p.Arg797Ser)
19g.41970246C=CA2336721157ATP1A3c.2520G= (p.Arg840=)
c.2481G= (p.Arg827=)
c.2514G= (p.Arg838=)
c.2391G= (p.Arg797=)
19g.41970246C>GCA406038796ATP1A3c.2520G>C (p.Arg840Ser)
c.2481G>C (p.Arg827Ser)
c.2514G>C (p.Arg838Ser)
c.2391G>C (p.Arg797Ser)
19g.41970246C>TCA507694715ATP1A3c.2520G>A (p.Arg840=)
c.2481G>A (p.Arg827=)
c.2514G>A (p.Arg838=)
c.2391G>A (p.Arg797=)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
19g.41970247C>ACA406038798ATP1A3c.2519G>T (p.Arg840Met)
c.2480G>T (p.Arg827Met)
c.2513G>T (p.Arg838Met)
c.2390G>T (p.Arg797Met)
19g.41970247C>GCA406038799ATP1A3c.2519G>C (p.Arg840Thr)
c.2480G>C (p.Arg827Thr)
c.2513G>C (p.Arg838Thr)
c.2390G>C (p.Arg797Thr)
19g.41970247C>TCA406038801ATP1A3c.2519G>A (p.Arg840Lys)
c.2480G>A (p.Arg827Lys)
c.2513G>A (p.Arg838Lys)
c.2390G>A (p.Arg797Lys)
19g.41970248T>ACA406038803ATP1A3c.2518A>T (p.Arg840Trp)
c.2479A>T (p.Arg827Trp)
c.2512A>T (p.Arg838Trp)
c.2389A>T (p.Arg797Trp)
ClinVar
19g.41970248T>CCA406038805ATP1A3c.2518A>G (p.Arg840Gly)
c.2479A>G (p.Arg827Gly)
c.2512A>G (p.Arg838Gly)
c.2389A>G (p.Arg797Gly)
19g.41970248T>GCA507694716ATP1A3c.2518A>C (p.Arg840=)
c.2479A>C (p.Arg827=)
c.2512A>C (p.Arg838=)
c.2389A>C (p.Arg797=)
19g.41970249G>ACA507694717ATP1A3c.2517C>T (p.Pro839=)
c.2478C>T (p.Pro826=)
c.2511C>T (p.Pro837=)
c.2388C>T (p.Pro796=)
19g.41970249G>CCA507694718ATP1A3c.2517C>G (p.Pro839=)
c.2478C>G (p.Pro826=)
c.2511C>G (p.Pro837=)
c.2388C>G (p.Pro796=)
19g.41970249G>TCA507694719ATP1A3c.2517C>A (p.Pro839=)
c.2478C>A (p.Pro826=)
c.2511C>A (p.Pro837=)
c.2388C>A (p.Pro796=)
19g.41970250G>ACA406038808ATP1A3c.2516C>T (p.Pro839Leu)
c.2477C>T (p.Pro826Leu)
c.2510C>T (p.Pro837Leu)
c.2387C>T (p.Pro796Leu)
COSMIC
19g.41970250G>CCA406038810ATP1A3c.2516C>G (p.Pro839Arg)
c.2477C>G (p.Pro826Arg)
c.2510C>G (p.Pro837Arg)
c.2387C>G (p.Pro796Arg)
19g.41970250G>TCA406038811ATP1A3c.2516C>A (p.Pro839His)
c.2477C>A (p.Pro826His)
c.2510C>A (p.Pro837His)
c.2387C>A (p.Pro796His)
19g.41970251G>ACA406038814ATP1A3c.2515C>T (p.Pro839Ser)
c.2476C>T (p.Pro826Ser)
c.2509C>T (p.Pro837Ser)
c.2386C>T (p.Pro796Ser)
19g.41970251G>CCA406038818ATP1A3c.2515C>G (p.Pro839Ala)
c.2476C>G (p.Pro826Ala)
c.2509C>G (p.Pro837Ala)
c.2386C>G (p.Pro796Ala)
19g.41970251G>TCA406038816ATP1A3c.2515C>A (p.Pro839Thr)
c.2476C>A (p.Pro826Thr)
c.2509C>A (p.Pro837Thr)
c.2386C>A (p.Pro796Thr)
19g.41970252C>ACA406038820ATP1A3c.2514G>T (p.Gln838His)
c.2475G>T (p.Gln825His)
c.2508G>T (p.Gln836His)
c.2385G>T (p.Gln795His)
19g.41970252C>GCA406038822ATP1A3c.2514G>C (p.Gln838His)
c.2475G>C (p.Gln825His)
c.2508G>C (p.Gln836His)
c.2385G>C (p.Gln795His)
19g.41970252C>TCA507694721ATP1A3c.2514G>A (p.Gln838=)
c.2475G>A (p.Gln825=)
c.2508G>A (p.Gln836=)
c.2385G>A (p.Gln795=)
19g.41970253T>ACA406038824ATP1A3c.2513A>T (p.Gln838Leu)
c.2474A>T (p.Gln825Leu)
c.2507A>T (p.Gln836Leu)
c.2384A>T (p.Gln795Leu)
19g.41970253T>CCA406038826ATP1A3c.2513A>G (p.Gln838Arg)
c.2474A>G (p.Gln825Arg)
c.2507A>G (p.Gln836Arg)
c.2384A>G (p.Gln795Arg)
dbSNP
19g.41970253T>GCA406038828ATP1A3c.2513A>C (p.Gln838Pro)
c.2474A>C (p.Gln825Pro)
c.2507A>C (p.Gln836Pro)
c.2384A>C (p.Gln795Pro)
19g.41970253T=CA2336721162ATP1A3c.2513A= (p.Gln838=)
c.2474A= (p.Gln825=)
c.2507A= (p.Gln836=)
c.2384A= (p.Gln795=)
19g.41970254G>ACA406038830ATP1A3c.2512C>T (p.Gln838Ter)
c.2473C>T (p.Gln825Ter)
c.2506C>T (p.Gln836Ter)
c.2383C>T (p.Gln795Ter)
19g.41970254G>CCA406038832ATP1A3c.2512C>G (p.Gln838Glu)
c.2473C>G (p.Gln825Glu)
c.2506C>G (p.Gln836Glu)
c.2383C>G (p.Gln795Glu)
19g.41970254G>TCA406038834ATP1A3c.2512C>A (p.Gln838Lys)
c.2473C>A (p.Gln825Lys)
c.2506C>A (p.Gln836Lys)
c.2383C>A (p.Gln795Lys)
19g.41970255T>ACA406038836ATP1A3c.2511A>T (p.Arg837Ser)
c.2472A>T (p.Arg824Ser)
c.2505A>T (p.Arg835Ser)
c.2382A>T (p.Arg794Ser)
19g.41970255T>CCA507694723ATP1A3c.2511A>G (p.Arg837=)
c.2472A>G (p.Arg824=)
c.2505A>G (p.Arg835=)
c.2382A>G (p.Arg794=)
19g.41970255T>GCA406038838ATP1A3c.2511A>C (p.Arg837Ser)
c.2472A>C (p.Arg824Ser)
c.2505A>C (p.Arg835Ser)
c.2382A>C (p.Arg794Ser)
19g.41970256C>ACA406038842ATP1A3c.2510G>T (p.Arg837Ile)
c.2471G>T (p.Arg824Ile)
c.2504G>T (p.Arg835Ile)
c.2381G>T (p.Arg794Ile)
19g.41970256C>GCA406038843ATP1A3c.2510G>C (p.Arg837Thr)
c.2471G>C (p.Arg824Thr)
c.2504G>C (p.Arg835Thr)
c.2381G>C (p.Arg794Thr)
19g.41970256C>TCA406038840ATP1A3c.2510G>A (p.Arg837Lys)
c.2471G>A (p.Arg824Lys)
c.2504G>A (p.Arg835Lys)
c.2381G>A (p.Arg794Lys)
19g.41970257T>ACA406038848ATP1A3c.2509A>T (p.Arg837Ter)
c.2470A>T (p.Arg824Ter)
c.2503A>T (p.Arg835Ter)
c.2380A>T (p.Arg794Ter)
19g.41970257T>CCA406038846ATP1A3c.2509A>G (p.Arg837Gly)
c.2470A>G (p.Arg824Gly)
c.2503A>G (p.Arg835Gly)
c.2380A>G (p.Arg794Gly)
19g.41970257T>GCA507694726ATP1A3c.2509A>C (p.Arg837=)
c.2470A>C (p.Arg824=)
c.2503A>C (p.Arg835=)
c.2380A>C (p.Arg794=)
19g.41970258C>ACA406038850ATP1A3c.2508G>T (p.Lys836Asn)
c.2469G>T (p.Lys823Asn)
c.2502G>T (p.Lys834Asn)
c.2379G>T (p.Lys793Asn)
19g.41970258C=CA2336721165ATP1A3c.2508G= (p.Lys836=)
c.2469G= (p.Lys823=)
c.2502G= (p.Lys834=)
c.2379G= (p.Lys793=)
19g.41970258C>GCA406038852ATP1A3c.2508G>C (p.Lys836Asn)
c.2469G>C (p.Lys823Asn)
c.2502G>C (p.Lys834Asn)
c.2379G>C (p.Lys793Asn)
19g.41970258C>TCA9467375ATP1A3c.2508G>A (p.Lys836=)
c.2469G>A (p.Lys823=)
c.2502G>A (p.Lys834=)
c.2379G>A (p.Lys793=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.41970259T>ACA406038855ATP1A3c.2507A>T (p.Lys836Met)
c.2468A>T (p.Lys823Met)
c.2501A>T (p.Lys834Met)
c.2378A>T (p.Lys793Met)
19g.41970259T>CCA406038857ATP1A3c.2507A>G (p.Lys836Arg)
c.2468A>G (p.Lys823Arg)
c.2501A>G (p.Lys834Arg)
c.2378A>G (p.Lys793Arg)
19g.41970259T>GCA406038859ATP1A3c.2507A>C (p.Lys836Thr)
c.2468A>C (p.Lys823Thr)
c.2501A>C (p.Lys834Thr)
c.2378A>C (p.Lys793Thr)
19g.41970260T>ACA406038861ATP1A3c.2506A>T (p.Lys836Ter)
c.2467A>T (p.Lys823Ter)
c.2500A>T (p.Lys834Ter)
c.2377A>T (p.Lys793Ter)
19g.41970260T>CCA406038863ATP1A3c.2506A>G (p.Lys836Glu)
c.2467A>G (p.Lys823Glu)
c.2500A>G (p.Lys834Glu)
c.2377A>G (p.Lys793Glu)
19g.41970260T>GCA406038865ATP1A3c.2506A>C (p.Lys836Gln)
c.2467A>C (p.Lys823Gln)
c.2500A>C (p.Lys834Gln)
c.2377A>C (p.Lys793Gln)
19g.41970261C>ACA406038866ATP1A3c.2505G>T (p.Met835Ile)
c.2466G>T (p.Met822Ile)
c.2499G>T (p.Met833Ile)
c.2376G>T (p.Met792Ile)
19g.41970261C>GCA406038869ATP1A3c.2505G>C (p.Met835Ile)
c.2466G>C (p.Met822Ile)
c.2499G>C (p.Met833Ile)
c.2376G>C (p.Met792Ile)
19g.41970261C>TCA406038871ATP1A3c.2505G>A (p.Met835Ile)
c.2466G>A (p.Met822Ile)
c.2499G>A (p.Met833Ile)
c.2376G>A (p.Met792Ile)
COSMIC
19g.41970262A>CCA406038877ATP1A3c.2504T>G (p.Met835Arg)
c.2465T>G (p.Met822Arg)
c.2498T>G (p.Met833Arg)
c.2375T>G (p.Met792Arg)
19g.41970262A>GCA406038873ATP1A3c.2504T>C (p.Met835Thr)
c.2465T>C (p.Met822Thr)
c.2498T>C (p.Met833Thr)
c.2375T>C (p.Met792Thr)
19g.41970262A>TCA406038875ATP1A3c.2504T>A (p.Met835Lys)
c.2465T>A (p.Met822Lys)
c.2498T>A (p.Met833Lys)
c.2375T>A (p.Met792Lys)
19g.41970263T>ACA406038879ATP1A3c.2503A>T (p.Met835Leu)
c.2464A>T (p.Met822Leu)
c.2497A>T (p.Met833Leu)
c.2374A>T (p.Met792Leu)
19g.41970263T>CCA406038880ATP1A3c.2503A>G (p.Met835Val)
c.2464A>G (p.Met822Val)
c.2497A>G (p.Met833Val)
c.2374A>G (p.Met792Val)
19g.41970263T>GCA406038882ATP1A3c.2503A>C (p.Met835Leu)
c.2464A>C (p.Met822Leu)
c.2497A>C (p.Met833Leu)
c.2374A>C (p.Met792Leu)
19g.41970264G>ACA507694736ATP1A3c.2502C>T (p.Ile834=)
c.2463C>T (p.Ile821=)
c.2496C>T (p.Ile832=)
c.2373C>T (p.Ile791=)
19g.41970264G>CCA406038884ATP1A3c.2502C>G (p.Ile834Met)
c.2463C>G (p.Ile821Met)
c.2496C>G (p.Ile832Met)
c.2373C>G (p.Ile791Met)
19g.41970264G>TCA507694737ATP1A3c.2502C>A (p.Ile834=)
c.2463C>A (p.Ile821=)
c.2496C>A (p.Ile832=)
c.2373C>A (p.Ile791=)
COSMIC
19g.41970265A>CCA406038886ATP1A3c.2501T>G (p.Ile834Ser)
c.2462T>G (p.Ile821Ser)
c.2495T>G (p.Ile832Ser)
c.2372T>G (p.Ile791Ser)
19g.41970265A>GCA406038888ATP1A3c.2501T>C (p.Ile834Thr)
c.2462T>C (p.Ile821Thr)
c.2495T>C (p.Ile832Thr)
c.2372T>C (p.Ile791Thr)
19g.41970265A>TCA406038890ATP1A3c.2501T>A (p.Ile834Asn)
c.2462T>A (p.Ile821Asn)
c.2495T>A (p.Ile832Asn)
c.2372T>A (p.Ile791Asn)
19g.41970266T>ACA406038892ATP1A3c.2500A>T (p.Ile834Phe)
c.2461A>T (p.Ile821Phe)
c.2494A>T (p.Ile832Phe)
c.2371A>T (p.Ile791Phe)
19g.41970266T>CCA406038894ATP1A3c.2500A>G (p.Ile834Val)
c.2461A>G (p.Ile821Val)
c.2494A>G (p.Ile832Val)
c.2371A>G (p.Ile791Val)
19g.41970266T>GCA406038896ATP1A3c.2500A>C (p.Ile834Leu)
c.2461A>C (p.Ile821Leu)
c.2494A>C (p.Ile832Leu)
c.2371A>C (p.Ile791Leu)
ClinVar dbSNP
19g.41970267G>ACA507694738ATP1A3c.2499C>T (p.Asp833=)
c.2460C>T (p.Asp820=)
c.2493C>T (p.Asp831=)
c.2370C>T (p.Asp790=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41970267G>CCA406038898ATP1A3c.2499C>G (p.Asp833Glu)
c.2460C>G (p.Asp820Glu)
c.2493C>G (p.Asp831Glu)
c.2370C>G (p.Asp790Glu)
19g.41970267G=CA2336721166ATP1A3c.2499C= (p.Asp833=)
c.2460C= (p.Asp820=)
c.2493C= (p.Asp831=)
c.2370C= (p.Asp790=)
19g.41970267G>TCA406038899ATP1A3c.2499C>A (p.Asp833Glu)
c.2460C>A (p.Asp820Glu)
c.2493C>A (p.Asp831Glu)
c.2370C>A (p.Asp790Glu)
19g.41970268T>ACA406038905ATP1A3c.2498A>T (p.Asp833Val)
c.2459A>T (p.Asp820Val)
c.2492A>T (p.Asp831Val)
c.2369A>T (p.Asp790Val)
19g.41970268T>CCA406038903ATP1A3c.2498A>G (p.Asp833Gly)
c.2459A>G (p.Asp820Gly)
c.2492A>G (p.Asp831Gly)
c.2369A>G (p.Asp790Gly)
19g.41970268T>GCA406038901ATP1A3c.2498A>C (p.Asp833Ala)
c.2459A>C (p.Asp820Ala)
c.2492A>C (p.Asp831Ala)
c.2369A>C (p.Asp790Ala)
19g.41970269C>ACA406038907ATP1A3c.2497G>T (p.Asp833Tyr)
c.2458G>T (p.Asp820Tyr)
c.2491G>T (p.Asp831Tyr)
c.2368G>T (p.Asp790Tyr)
19g.41970269C=CA2336721167ATP1A3c.2497G= (p.Asp833=)
c.2458G= (p.Asp820=)
c.2491G= (p.Asp831=)
c.2368G= (p.Asp790=)
19g.41970269C>GCA406038910ATP1A3c.2497G>C (p.Asp833His)
c.2458G>C (p.Asp820His)
c.2491G>C (p.Asp831His)
c.2368G>C (p.Asp790His)
19g.41970269C>TCA9467376ATP1A3c.2497G>A (p.Asp833Asn)
c.2458G>A (p.Asp820Asn)
c.2491G>A (p.Asp831Asn)
c.2368G>A (p.Asp790Asn)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41970270G>ACA9467377ATP1A3c.2496C>T (p.Ser832=)
c.2457C>T (p.Ser819=)
c.2490C>T (p.Ser830=)
c.2367C>T (p.Ser789=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.41970270G>CCA406038913ATP1A3c.2496C>G (p.Ser832Arg)
c.2457C>G (p.Ser819Arg)
c.2490C>G (p.Ser830Arg)
c.2367C>G (p.Ser789Arg)
19g.41970270G=CA2336721168ATP1A3c.2496C= (p.Ser832=)
c.2457C= (p.Ser819=)
c.2490C= (p.Ser830=)
c.2367C= (p.Ser789=)
19g.41970270G>TCA406038915ATP1A3c.2496C>A (p.Ser832Arg)
c.2457C>A (p.Ser819Arg)
c.2490C>A (p.Ser830Arg)
c.2367C>A (p.Ser789Arg)
gnomAD v4
19g.41970271C>ACA406038917ATP1A3c.2495G>T (p.Ser832Ile)
c.2456G>T (p.Ser819Ile)
c.2489G>T (p.Ser830Ile)
c.2366G>T (p.Ser789Ile)
19g.41970271C=CA2336721169ATP1A3c.2495G= (p.Ser832=)
c.2456G= (p.Ser819=)
c.2489G= (p.Ser830=)
c.2366G= (p.Ser789=)
19g.41970271C>GCA406038919ATP1A3c.2495G>C (p.Ser832Thr)
c.2456G>C (p.Ser819Thr)
c.2489G>C (p.Ser830Thr)
c.2366G>C (p.Ser789Thr)
19g.41970271C>TCA406038921ATP1A3c.2495G>A (p.Ser832Asn)
c.2456G>A (p.Ser819Asn)
c.2489G>A (p.Ser830Asn)
c.2366G>A (p.Ser789Asn)
ClinVar dbSNP
19g.41970272T>ACA406038923ATP1A3c.2494A>T (p.Ser832Cys)
c.2455A>T (p.Ser819Cys)
c.2488A>T (p.Ser830Cys)
c.2365A>T (p.Ser789Cys)
19g.41970272T>CCA406038925ATP1A3c.2494A>G (p.Ser832Gly)
c.2455A>G (p.Ser819Gly)
c.2488A>G (p.Ser830Gly)
c.2365A>G (p.Ser789Gly)
19g.41970272T>GCA406038927ATP1A3c.2494A>C (p.Ser832Arg)
c.2455A>C (p.Ser819Arg)
c.2488A>C (p.Ser830Arg)
c.2365A>C (p.Ser789Arg)
19g.41970273T>ACA406038929ATP1A3c.2493A>T (p.Glu831Asp)
c.2454A>T (p.Glu818Asp)
c.2487A>T (p.Glu829Asp)
c.2364A>T (p.Glu788Asp)
19g.41970273T>CCA507694741ATP1A3c.2493A>G (p.Glu831=)
c.2454A>G (p.Glu818=)
c.2487A>G (p.Glu829=)
c.2364A>G (p.Glu788=)
19g.41970273T>GCA406038931ATP1A3c.2493A>C (p.Glu831Asp)
c.2454A>C (p.Glu818Asp)
c.2487A>C (p.Glu829Asp)
c.2364A>C (p.Glu788Asp)
19g.41970274T>ACA406038937ATP1A3c.2492A>T (p.Glu831Val)
c.2453A>T (p.Glu818Val)
c.2486A>T (p.Glu829Val)
c.2363A>T (p.Glu788Val)
19g.41970274T>CCA406038936ATP1A3c.2492A>G (p.Glu831Gly)
c.2453A>G (p.Glu818Gly)
c.2486A>G (p.Glu829Gly)
c.2363A>G (p.Glu788Gly)
19g.41970274T>GCA406038934ATP1A3c.2492A>C (p.Glu831Ala)
c.2453A>C (p.Glu818Ala)
c.2486A>C (p.Glu829Ala)
c.2363A>C (p.Glu788Ala)
19g.41970275C>ACA406038939ATP1A3c.2491G>T (p.Glu831Ter)
c.2452G>T (p.Glu818Ter)
c.2485G>T (p.Glu829Ter)
c.2362G>T (p.Glu788Ter)
19g.41970275C=CA2336720775ATP1A3c.2491G= (p.Glu831=)
c.2452G= (p.Glu818=)
c.2485G= (p.Glu829=)
c.2362G= (p.Glu788=)
19g.41970275C>GCA406038940ATP1A3c.2491G>C (p.Glu831Gln)
c.2452G>C (p.Glu818Gln)
c.2485G>C (p.Glu829Gln)
c.2362G>C (p.Glu788Gln)
19g.41970275C>TCA204733ATP1A3c.2491G>A (p.Glu831Lys)
c.2452G>A (p.Glu818Lys)
c.2485G>A (p.Glu829Lys)
c.2362G>A (p.Glu788Lys)
ClinVar dbSNP COSMIC
19g.41970276G>ACA9467378ATP1A3c.2490C>T (p.Ala830=)
c.2451C>T (p.Ala817=)
c.2484C>T (p.Ala828=)
c.2361C>T (p.Ala787=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41970276G>CCA507694743ATP1A3c.2490C>G (p.Ala830=)
c.2451C>G (p.Ala817=)
c.2484C>G (p.Ala828=)
c.2361C>G (p.Ala787=)
gnomAD v4
19g.41970276G=CA2336720776ATP1A3c.2490C= (p.Ala830=)
c.2451C= (p.Ala817=)
c.2484C= (p.Ala828=)
c.2361C= (p.Ala787=)
19g.41970276G>TCA507694744ATP1A3c.2490C>A (p.Ala830=)
c.2451C>A (p.Ala817=)
c.2484C>A (p.Ala828=)
c.2361C>A (p.Ala787=)
19g.41970277G>ACA406038945ATP1A3c.2489C>T (p.Ala830Val)
c.2450C>T (p.Ala817Val)
c.2483C>T (p.Ala828Val)
c.2360C>T (p.Ala787Val)
19g.41970277G>CCA406038947ATP1A3c.2489C>G (p.Ala830Gly)
c.2450C>G (p.Ala817Gly)
c.2483C>G (p.Ala828Gly)
c.2360C>G (p.Ala787Gly)
19g.41970277G>TCA406038949ATP1A3c.2489C>A (p.Ala830Asp)
c.2450C>A (p.Ala817Asp)
c.2483C>A (p.Ala828Asp)
c.2360C>A (p.Ala787Asp)
19g.41970278C>ACA406038951ATP1A3c.2488G>T (p.Ala830Ser)
c.2449G>T (p.Ala817Ser)
c.2482G>T (p.Ala828Ser)
c.2359G>T (p.Ala787Ser)
19g.41970278C=CA2336720777ATP1A3c.2488G= (p.Ala830=)
c.2449G= (p.Ala817=)
c.2482G= (p.Ala828=)
c.2359G= (p.Ala787=)
19g.41970278C>GCA406038953ATP1A3c.2488G>C (p.Ala830Pro)
c.2449G>C (p.Ala817Pro)
c.2482G>C (p.Ala828Pro)
c.2359G>C (p.Ala787Pro)
19g.41970278C>TCA9467379ATP1A3c.2488G>A (p.Ala830Thr)
c.2449G>A (p.Ala817Thr)
c.2482G>A (p.Ala828Thr)
c.2359G>A (p.Ala787Thr)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.41970279A>CCA507694746ATP1A3c.2487T>G (p.Ala829=)
c.2448T>G (p.Ala816=)
c.2481T>G (p.Ala827=)
c.2358T>G (p.Ala786=)
19g.41970279A>GCA507694747ATP1A3c.2487T>C (p.Ala829=)
c.2448T>C (p.Ala816=)
c.2481T>C (p.Ala827=)
c.2358T>C (p.Ala786=)
19g.41970279A>TCA507694748ATP1A3c.2487T>A (p.Ala829=)
c.2448T>A (p.Ala816=)
c.2481T>A (p.Ala827=)
c.2358T>A (p.Ala786=)
19g.41970280G>ACA406038956ATP1A3c.2486C>T (p.Ala829Val)
c.2447C>T (p.Ala816Val)
c.2480C>T (p.Ala827Val)
c.2357C>T (p.Ala786Val)
19g.41970280G>CCA406038958ATP1A3c.2486C>G (p.Ala829Gly)
c.2447C>G (p.Ala816Gly)
c.2480C>G (p.Ala827Gly)
c.2357C>G (p.Ala786Gly)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41970280G=CA2336720778ATP1A3c.2486C= (p.Ala829=)
c.2447C= (p.Ala816=)
c.2480C= (p.Ala827=)
c.2357C= (p.Ala786=)
19g.41970280G>TCA406038959ATP1A3c.2486C>A (p.Ala829Asp)
c.2447C>A (p.Ala816Asp)
c.2480C>A (p.Ala827Asp)
c.2357C>A (p.Ala786Asp)
19g.41970281C>ACA406038963ATP1A3c.2485G>T (p.Ala829Ser)
c.2446G>T (p.Ala816Ser)
c.2479G>T (p.Ala827Ser)
c.2356G>T (p.Ala786Ser)
19g.41970281C=CA2336720779ATP1A3c.2485G= (p.Ala829=)
c.2446G= (p.Ala816=)
c.2479G= (p.Ala827=)
c.2356G= (p.Ala786=)
19g.41970281C>GCA406038964ATP1A3c.2485G>C (p.Ala829Pro)
c.2446G>C (p.Ala816Pro)
c.2479G>C (p.Ala827Pro)
c.2356G>C (p.Ala786Pro)
19g.41970281C>TCA406038961ATP1A3c.2485G>A (p.Ala829Thr)
c.2446G>A (p.Ala816Thr)
c.2479G>A (p.Ala827Thr)
c.2356G>A (p.Ala786Thr)
dbSNP gnomAD v3 gnomAD v4
19g.41970282C>ACA406038968ATP1A3c.2484G>T (p.Glu828Asp)
c.2445G>T (p.Glu815Asp)
c.2478G>T (p.Glu826Asp)
c.2355G>T (p.Glu785Asp)
19g.41970282C=CA2336720780ATP1A3c.2484G= (p.Glu828=)
c.2445G= (p.Glu815=)
c.2478G= (p.Glu826=)
c.2355G= (p.Glu785=)
19g.41970282C>GCA406038966ATP1A3c.2484G>C (p.Glu828Asp)
c.2445G>C (p.Glu815Asp)
c.2478G>C (p.Glu826Asp)
c.2355G>C (p.Glu785Asp)
19g.41970282C>TCA9467380ATP1A3c.2484G>A (p.Glu828=)
c.2445G>A (p.Glu815=)
c.2478G>A (p.Glu826=)
c.2355G>A (p.Glu785=)
ClinVar dbSNP ExAC gnomAD v3 gnomAD v4
19g.41970283T>ACA406038971ATP1A3c.2483A>T (p.Glu828Val)
c.2444A>T (p.Glu815Val)
c.2477A>T (p.Glu826Val)
c.2354A>T (p.Glu785Val)
19g.41970283T>CCA406038974ATP1A3c.2483A>G (p.Glu828Gly)
c.2444A>G (p.Glu815Gly)
c.2477A>G (p.Glu826Gly)
c.2354A>G (p.Glu785Gly)
19g.41970283T>GCA406038972ATP1A3c.2483A>C (p.Glu828Ala)
c.2444A>C (p.Glu815Ala)
c.2477A>C (p.Glu826Ala)
c.2354A>C (p.Glu785Ala)
19g.41970284C>ACA406038975ATP1A3c.2482G>T (p.Glu828Ter)
c.2443G>T (p.Glu815Ter)
c.2476G>T (p.Glu826Ter)
c.2353G>T (p.Glu785Ter)
19g.41970284C=CA2336720781ATP1A3c.2482G= (p.Glu828=)
c.2443G= (p.Glu815=)
c.2476G= (p.Glu826=)
c.2353G= (p.Glu785=)
19g.41970284C>GCA406038977ATP1A3c.2482G>C (p.Glu828Gln)
c.2443G>C (p.Glu815Gln)
c.2476G>C (p.Glu826Gln)
c.2353G>C (p.Glu785Gln)
19g.41970284C>TCA342903ATP1A3c.2482G>A (p.Glu828Lys)
c.2443G>A (p.Glu815Lys)
c.2476G>A (p.Glu826Lys)
c.2353G>A (p.Glu785Lys)
ClinVar dbSNP COSMIC
19g.41970285G>ACA9467381ATP1A3c.2481C>T (p.Tyr827=)
c.2442C>T (p.Tyr814=)
c.2475C>T (p.Tyr825=)
c.2352C>T (p.Tyr784=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.41970285G>CCA406038981ATP1A3c.2481C>G (p.Tyr827Ter)
c.2442C>G (p.Tyr814Ter)
c.2475C>G (p.Tyr825Ter)
c.2352C>G (p.Tyr784Ter)
19g.41970285G=CA2336720782ATP1A3c.2481C= (p.Tyr827=)
c.2442C= (p.Tyr814=)
c.2475C= (p.Tyr825=)
c.2352C= (p.Tyr784=)
19g.41970285G>TCA406038983ATP1A3c.2481C>A (p.Tyr827Ter)
c.2442C>A (p.Tyr814Ter)
c.2475C>A (p.Tyr825Ter)
c.2352C>A (p.Tyr784Ter)
19g.41970286T>ACA406038985ATP1A3c.2480A>T (p.Tyr827Phe)
c.2441A>T (p.Tyr814Phe)
c.2474A>T (p.Tyr825Phe)
c.2351A>T (p.Tyr784Phe)
19g.41970286T>CCA406038986ATP1A3c.2480A>G (p.Tyr827Cys)
c.2441A>G (p.Tyr814Cys)
c.2474A>G (p.Tyr825Cys)
c.2351A>G (p.Tyr784Cys)
19g.41970286T>GCA406038987ATP1A3c.2480A>C (p.Tyr827Ser)
c.2441A>C (p.Tyr814Ser)
c.2474A>C (p.Tyr825Ser)
c.2351A>C (p.Tyr784Ser)
19g.41970287A>CCA406038990ATP1A3c.2479T>G (p.Tyr827Asp)
c.2440T>G (p.Tyr814Asp)
c.2473T>G (p.Tyr825Asp)
c.2350T>G (p.Tyr784Asp)
19g.41970287A>GCA406038992ATP1A3c.2479T>C (p.Tyr827His)
c.2440T>C (p.Tyr814His)
c.2473T>C (p.Tyr825His)
c.2350T>C (p.Tyr784His)
19g.41970287A>TCA406038993ATP1A3c.2479T>A (p.Tyr827Asn)
c.2440T>A (p.Tyr814Asn)
c.2473T>A (p.Tyr825Asn)
c.2350T>A (p.Tyr784Asn)
19g.41970288C>ACA507694752ATP1A3c.2478G>T (p.Ala826=)
c.2439G>T (p.Ala813=)
c.2472G>T (p.Ala824=)
c.2349G>T (p.Ala783=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.41970288C=CA2336720784ATP1A3c.2478G= (p.Ala826=)
c.2439G= (p.Ala813=)
c.2472G= (p.Ala824=)
c.2349G= (p.Ala783=)
19g.41970288C>GCA507694753ATP1A3c.2478G>C (p.Ala826=)
c.2439G>C (p.Ala813=)
c.2472G>C (p.Ala824=)
c.2349G>C (p.Ala783=)
gnomAD v4
19g.41970288C>TCA9467382ATP1A3c.2478G>A (p.Ala826=)
c.2439G>A (p.Ala813=)
c.2472G>A (p.Ala824=)
c.2349G>A (p.Ala783=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC

Number of alleles fetched