Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.101083758T>A | CA388651857 | NALCN | c.3536A>T (p.Lys1179Met) c.3257A>T (p.Lys1086Met) c.3623A>T (p.Lys1208Met) c.3449A>T (p.Lys1150Met) c.3593A>T (p.Lys1198Met) c.3506A>T (p.Lys1169Met) c.3314A>T (p.Lys1105Met) c.3089A>T (p.Lys1030Met) c.2771A>T (p.Lys924Met) c.3680A>T (p.Lys1227Met) | |
13 | g.101083758T>C | CA388651855 | NALCN | c.3536A>G (p.Lys1179Arg) c.3257A>G (p.Lys1086Arg) c.3623A>G (p.Lys1208Arg) c.3449A>G (p.Lys1150Arg) c.3593A>G (p.Lys1198Arg) c.3506A>G (p.Lys1169Arg) c.3314A>G (p.Lys1105Arg) c.3089A>G (p.Lys1030Arg) c.2771A>G (p.Lys924Arg) c.3680A>G (p.Lys1227Arg) | |
13 | g.101083758T>G | CA388651854 | NALCN | c.3536A>C (p.Lys1179Thr) c.3257A>C (p.Lys1086Thr) c.3623A>C (p.Lys1208Thr) c.3449A>C (p.Lys1150Thr) c.3593A>C (p.Lys1198Thr) c.3506A>C (p.Lys1169Thr) c.3314A>C (p.Lys1105Thr) c.3089A>C (p.Lys1030Thr) c.2771A>C (p.Lys924Thr) c.3680A>C (p.Lys1227Thr) | |
13 | g.101083759T>A | CA388651859 | NALCN | c.3535A>T (p.Lys1179Ter) c.3256A>T (p.Lys1086Ter) c.3622A>T (p.Lys1208Ter) c.3448A>T (p.Lys1150Ter) c.3592A>T (p.Lys1198Ter) c.3505A>T (p.Lys1169Ter) c.3313A>T (p.Lys1105Ter) c.3088A>T (p.Lys1030Ter) c.2770A>T (p.Lys924Ter) c.3679A>T (p.Lys1227Ter) | |
13 | g.101083759T>C | CA388651860 | NALCN | c.3535A>G (p.Lys1179Glu) c.3256A>G (p.Lys1086Glu) c.3622A>G (p.Lys1208Glu) c.3448A>G (p.Lys1150Glu) c.3592A>G (p.Lys1198Glu) c.3505A>G (p.Lys1169Glu) c.3313A>G (p.Lys1105Glu) c.3088A>G (p.Lys1030Glu) c.2770A>G (p.Lys924Glu) c.3679A>G (p.Lys1227Glu) | |
13 | g.101083759T>G | CA388651861 | NALCN | c.3535A>C (p.Lys1179Gln) c.3256A>C (p.Lys1086Gln) c.3622A>C (p.Lys1208Gln) c.3448A>C (p.Lys1150Gln) c.3592A>C (p.Lys1198Gln) c.3505A>C (p.Lys1169Gln) c.3313A>C (p.Lys1105Gln) c.3088A>C (p.Lys1030Gln) c.2770A>C (p.Lys924Gln) c.3679A>C (p.Lys1227Gln) | |
13 | g.101083760C>A | CA484553414 | NALCN | c.3534G>T (p.Leu1178=) c.3255G>T (p.Leu1085=) c.3621G>T (p.Leu1207=) c.3447G>T (p.Leu1149=) c.3591G>T (p.Leu1197=) c.3504G>T (p.Leu1168=) c.3312G>T (p.Leu1104=) c.3087G>T (p.Leu1029=) c.2769G>T (p.Leu923=) c.3678G>T (p.Leu1226=) | |
13 | g.101083760C>G | CA484553413 | NALCN | c.3534G>C (p.Leu1178=) c.3255G>C (p.Leu1085=) c.3621G>C (p.Leu1207=) c.3447G>C (p.Leu1149=) c.3591G>C (p.Leu1197=) c.3504G>C (p.Leu1168=) c.3312G>C (p.Leu1104=) c.3087G>C (p.Leu1029=) c.2769G>C (p.Leu923=) c.3678G>C (p.Leu1226=) | |
13 | g.101083760C>T | CA484553412 | NALCN | c.3534G>A (p.Leu1178=) c.3255G>A (p.Leu1085=) c.3621G>A (p.Leu1207=) c.3447G>A (p.Leu1149=) c.3591G>A (p.Leu1197=) c.3504G>A (p.Leu1168=) c.3312G>A (p.Leu1104=) c.3087G>A (p.Leu1029=) c.2769G>A (p.Leu923=) c.3678G>A (p.Leu1226=) | |
13 | g.101083761A= | CA2114389782 | NALCN | c.3533T= (p.Leu1178=) c.3254T= (p.Leu1085=) c.3620T= (p.Leu1207=) c.3446T= (p.Leu1149=) c.3590T= (p.Leu1197=) c.3503T= (p.Leu1168=) c.3311T= (p.Leu1104=) c.3086T= (p.Leu1029=) c.2768T= (p.Leu923=) c.3677T= (p.Leu1226=) | |
13 | g.101083761A>C | CA388651863 | NALCN | c.3533T>G (p.Leu1178Arg) c.3254T>G (p.Leu1085Arg) c.3620T>G (p.Leu1207Arg) c.3446T>G (p.Leu1149Arg) c.3590T>G (p.Leu1197Arg) c.3503T>G (p.Leu1168Arg) c.3311T>G (p.Leu1104Arg) c.3086T>G (p.Leu1029Arg) c.2768T>G (p.Leu923Arg) c.3677T>G (p.Leu1226Arg) | |
13 | g.101083761A>G | CA388651864 | NALCN | c.3533T>C (p.Leu1178Pro) c.3254T>C (p.Leu1085Pro) c.3620T>C (p.Leu1207Pro) c.3446T>C (p.Leu1149Pro) c.3590T>C (p.Leu1197Pro) c.3503T>C (p.Leu1168Pro) c.3311T>C (p.Leu1104Pro) c.3086T>C (p.Leu1029Pro) c.2768T>C (p.Leu923Pro) c.3677T>C (p.Leu1226Pro) | ClinVar dbSNP |
13 | g.101083761A>T | CA388651866 | NALCN | c.3533T>A (p.Leu1178Gln) c.3254T>A (p.Leu1085Gln) c.3620T>A (p.Leu1207Gln) c.3446T>A (p.Leu1149Gln) c.3590T>A (p.Leu1197Gln) c.3503T>A (p.Leu1168Gln) c.3311T>A (p.Leu1104Gln) c.3086T>A (p.Leu1029Gln) c.2768T>A (p.Leu923Gln) c.3677T>A (p.Leu1226Gln) | |
13 | g.101083762G>A | CA484553415 | NALCN | c.3532C>T (p.Leu1178=) c.3253C>T (p.Leu1085=) c.3619C>T (p.Leu1207=) c.3445C>T (p.Leu1149=) c.3589C>T (p.Leu1197=) c.3502C>T (p.Leu1168=) c.3310C>T (p.Leu1104=) c.3085C>T (p.Leu1029=) c.2767C>T (p.Leu923=) c.3676C>T (p.Leu1226=) | |
13 | g.101083762G>C | CA388651867 | NALCN | c.3532C>G (p.Leu1178Val) c.3253C>G (p.Leu1085Val) c.3619C>G (p.Leu1207Val) c.3445C>G (p.Leu1149Val) c.3589C>G (p.Leu1197Val) c.3502C>G (p.Leu1168Val) c.3310C>G (p.Leu1104Val) c.3085C>G (p.Leu1029Val) c.2767C>G (p.Leu923Val) c.3676C>G (p.Leu1226Val) | |
13 | g.101083762G>T | CA388651869 | NALCN | c.3532C>A (p.Leu1178Met) c.3253C>A (p.Leu1085Met) c.3619C>A (p.Leu1207Met) c.3445C>A (p.Leu1149Met) c.3589C>A (p.Leu1197Met) c.3502C>A (p.Leu1168Met) c.3310C>A (p.Leu1104Met) c.3085C>A (p.Leu1029Met) c.2767C>A (p.Leu923Met) c.3676C>A (p.Leu1226Met) | |
13 | g.101083763G>A | CA484553416 | NALCN | c.3531C>T (p.Asp1177=) c.3252C>T (p.Asp1084=) c.3618C>T (p.Asp1206=) c.3444C>T (p.Asp1148=) c.3588C>T (p.Asp1196=) c.3501C>T (p.Asp1167=) c.3309C>T (p.Asp1103=) c.3084C>T (p.Asp1028=) c.2766C>T (p.Asp922=) c.3675C>T (p.Asp1225=) | |
13 | g.101083763G>C | CA388651870 | NALCN | c.3531C>G (p.Asp1177Glu) c.3252C>G (p.Asp1084Glu) c.3618C>G (p.Asp1206Glu) c.3444C>G (p.Asp1148Glu) c.3588C>G (p.Asp1196Glu) c.3501C>G (p.Asp1167Glu) c.3309C>G (p.Asp1103Glu) c.3084C>G (p.Asp1028Glu) c.2766C>G (p.Asp922Glu) c.3675C>G (p.Asp1225Glu) | |
13 | g.101083763G>T | CA388651871 | NALCN | c.3531C>A (p.Asp1177Glu) c.3252C>A (p.Asp1084Glu) c.3618C>A (p.Asp1206Glu) c.3444C>A (p.Asp1148Glu) c.3588C>A (p.Asp1196Glu) c.3501C>A (p.Asp1167Glu) c.3309C>A (p.Asp1103Glu) c.3084C>A (p.Asp1028Glu) c.2766C>A (p.Asp922Glu) c.3675C>A (p.Asp1225Glu) | |
13 | g.101083764T>A | CA388651873 | NALCN | c.3530A>T (p.Asp1177Val) c.3251A>T (p.Asp1084Val) c.3617A>T (p.Asp1206Val) c.3443A>T (p.Asp1148Val) c.3587A>T (p.Asp1196Val) c.3500A>T (p.Asp1167Val) c.3308A>T (p.Asp1103Val) c.3083A>T (p.Asp1028Val) c.2765A>T (p.Asp922Val) c.3674A>T (p.Asp1225Val) | |
13 | g.101083764T>C | CA388651875 | NALCN | c.3530A>G (p.Asp1177Gly) c.3251A>G (p.Asp1084Gly) c.3617A>G (p.Asp1206Gly) c.3443A>G (p.Asp1148Gly) c.3587A>G (p.Asp1196Gly) c.3500A>G (p.Asp1167Gly) c.3308A>G (p.Asp1103Gly) c.3083A>G (p.Asp1028Gly) c.2765A>G (p.Asp922Gly) c.3674A>G (p.Asp1225Gly) | |
13 | g.101083764T>G | CA388651876 | NALCN | c.3530A>C (p.Asp1177Ala) c.3251A>C (p.Asp1084Ala) c.3617A>C (p.Asp1206Ala) c.3443A>C (p.Asp1148Ala) c.3587A>C (p.Asp1196Ala) c.3500A>C (p.Asp1167Ala) c.3308A>C (p.Asp1103Ala) c.3083A>C (p.Asp1028Ala) c.2765A>C (p.Asp922Ala) c.3674A>C (p.Asp1225Ala) | |
13 | g.101083765C>A | CA388651881 | NALCN | c.3529G>T (p.Asp1177Tyr) c.3250G>T (p.Asp1084Tyr) c.3616G>T (p.Asp1206Tyr) c.3442G>T (p.Asp1148Tyr) c.3586G>T (p.Asp1196Tyr) c.3499G>T (p.Asp1167Tyr) c.3307G>T (p.Asp1103Tyr) c.3082G>T (p.Asp1028Tyr) c.2764G>T (p.Asp922Tyr) c.3673G>T (p.Asp1225Tyr) | |
13 | g.101083765C>G | CA388651879 | NALCN | c.3529G>C (p.Asp1177His) c.3250G>C (p.Asp1084His) c.3616G>C (p.Asp1206His) c.3442G>C (p.Asp1148His) c.3586G>C (p.Asp1196His) c.3499G>C (p.Asp1167His) c.3307G>C (p.Asp1103His) c.3082G>C (p.Asp1028His) c.2764G>C (p.Asp922His) c.3673G>C (p.Asp1225His) | |
13 | g.101083765C>T | CA388651878 | NALCN | c.3529G>A (p.Asp1177Asn) c.3250G>A (p.Asp1084Asn) c.3616G>A (p.Asp1206Asn) c.3442G>A (p.Asp1148Asn) c.3586G>A (p.Asp1196Asn) c.3499G>A (p.Asp1167Asn) c.3307G>A (p.Asp1103Asn) c.3082G>A (p.Asp1028Asn) c.2764G>A (p.Asp922Asn) c.3673G>A (p.Asp1225Asn) | |
13 | g.101083766T>A | CA388651882 | NALCN | c.3528A>T (p.Glu1176Asp) c.3249A>T (p.Glu1083Asp) c.3615A>T (p.Glu1205Asp) c.3441A>T (p.Glu1147Asp) c.3585A>T (p.Glu1195Asp) c.3498A>T (p.Glu1166Asp) c.3306A>T (p.Glu1102Asp) c.3081A>T (p.Glu1027Asp) c.2763A>T (p.Glu921Asp) c.3672A>T (p.Glu1224Asp) | |
13 | g.101083766T>C | CA484553418 | NALCN | c.3528A>G (p.Glu1176=) c.3249A>G (p.Glu1083=) c.3615A>G (p.Glu1205=) c.3441A>G (p.Glu1147=) c.3585A>G (p.Glu1195=) c.3498A>G (p.Glu1166=) c.3306A>G (p.Glu1102=) c.3081A>G (p.Glu1027=) c.2763A>G (p.Glu921=) c.3672A>G (p.Glu1224=) | gnomAD v4 |
13 | g.101083766T>G | CA388651883 | NALCN | c.3528A>C (p.Glu1176Asp) c.3249A>C (p.Glu1083Asp) c.3615A>C (p.Glu1205Asp) c.3441A>C (p.Glu1147Asp) c.3585A>C (p.Glu1195Asp) c.3498A>C (p.Glu1166Asp) c.3306A>C (p.Glu1102Asp) c.3081A>C (p.Glu1027Asp) c.2763A>C (p.Glu921Asp) c.3672A>C (p.Glu1224Asp) | |
13 | g.101083767T>A | CA388651885 | NALCN | c.3527A>T (p.Glu1176Val) c.3248A>T (p.Glu1083Val) c.3614A>T (p.Glu1205Val) c.3440A>T (p.Glu1147Val) c.3584A>T (p.Glu1195Val) c.3497A>T (p.Glu1166Val) c.3305A>T (p.Glu1102Val) c.3080A>T (p.Glu1027Val) c.2762A>T (p.Glu921Val) c.3671A>T (p.Glu1224Val) | |
13 | g.101083767T>C | CA388651886 | NALCN | c.3527A>G (p.Glu1176Gly) c.3248A>G (p.Glu1083Gly) c.3614A>G (p.Glu1205Gly) c.3440A>G (p.Glu1147Gly) c.3584A>G (p.Glu1195Gly) c.3497A>G (p.Glu1166Gly) c.3305A>G (p.Glu1102Gly) c.3080A>G (p.Glu1027Gly) c.2762A>G (p.Glu921Gly) c.3671A>G (p.Glu1224Gly) | |
13 | g.101083767T>G | CA388651887 | NALCN | c.3527A>C (p.Glu1176Ala) c.3248A>C (p.Glu1083Ala) c.3614A>C (p.Glu1205Ala) c.3440A>C (p.Glu1147Ala) c.3584A>C (p.Glu1195Ala) c.3497A>C (p.Glu1166Ala) c.3305A>C (p.Glu1102Ala) c.3080A>C (p.Glu1027Ala) c.2762A>C (p.Glu921Ala) c.3671A>C (p.Glu1224Ala) | |
13 | g.101083768C>A | CA388651889 | NALCN | c.3526G>T (p.Glu1176Ter) c.3247G>T (p.Glu1083Ter) c.3613G>T (p.Glu1205Ter) c.3439G>T (p.Glu1147Ter) c.3583G>T (p.Glu1195Ter) c.3496G>T (p.Glu1166Ter) c.3304G>T (p.Glu1102Ter) c.3079G>T (p.Glu1027Ter) c.2761G>T (p.Glu921Ter) c.3670G>T (p.Glu1224Ter) | |
13 | g.101083768C>G | CA388651890 | NALCN | c.3526G>C (p.Glu1176Gln) c.3247G>C (p.Glu1083Gln) c.3613G>C (p.Glu1205Gln) c.3439G>C (p.Glu1147Gln) c.3583G>C (p.Glu1195Gln) c.3496G>C (p.Glu1166Gln) c.3304G>C (p.Glu1102Gln) c.3079G>C (p.Glu1027Gln) c.2761G>C (p.Glu921Gln) c.3670G>C (p.Glu1224Gln) | |
13 | g.101083768C>T | CA388651891 | NALCN | c.3526G>A (p.Glu1176Lys) c.3247G>A (p.Glu1083Lys) c.3613G>A (p.Glu1205Lys) c.3439G>A (p.Glu1147Lys) c.3583G>A (p.Glu1195Lys) c.3496G>A (p.Glu1166Lys) c.3304G>A (p.Glu1102Lys) c.3079G>A (p.Glu1027Lys) c.2761G>A (p.Glu921Lys) c.3670G>A (p.Glu1224Lys) | |
13 | g.101083769C>A | CA388651893 | NALCN | c.3525G>T (p.Trp1175Cys) c.3246G>T (p.Trp1082Cys) c.3612G>T (p.Trp1204Cys) c.3438G>T (p.Trp1146Cys) c.3582G>T (p.Trp1194Cys) c.3495G>T (p.Trp1165Cys) c.3303G>T (p.Trp1101Cys) c.3078G>T (p.Trp1026Cys) c.2760G>T (p.Trp920Cys) c.3669G>T (p.Trp1223Cys) | |
13 | g.101083769C= | CA2114389783 | NALCN | c.3525G= (p.Trp1175=) c.3246G= (p.Trp1082=) c.3612G= (p.Trp1204=) c.3438G= (p.Trp1146=) c.3582G= (p.Trp1194=) c.3495G= (p.Trp1165=) c.3303G= (p.Trp1101=) c.3078G= (p.Trp1026=) c.2760G= (p.Trp920=) c.3669G= (p.Trp1223=) | |
13 | g.101083769C>G | CA388651894 | NALCN | c.3525G>C (p.Trp1175Cys) c.3246G>C (p.Trp1082Cys) c.3612G>C (p.Trp1204Cys) c.3438G>C (p.Trp1146Cys) c.3582G>C (p.Trp1194Cys) c.3495G>C (p.Trp1165Cys) c.3303G>C (p.Trp1101Cys) c.3078G>C (p.Trp1026Cys) c.2760G>C (p.Trp920Cys) c.3669G>C (p.Trp1223Cys) | |
13 | g.101083769C>T | CA255408558 | NALCN | c.3525G>A (p.Trp1175Ter) c.3246G>A (p.Trp1082Ter) c.3612G>A (p.Trp1204Ter) c.3438G>A (p.Trp1146Ter) c.3582G>A (p.Trp1194Ter) c.3495G>A (p.Trp1165Ter) c.3303G>A (p.Trp1101Ter) c.3078G>A (p.Trp1026Ter) c.2760G>A (p.Trp920Ter) c.3669G>A (p.Trp1223Ter) | dbSNP gnomAD v4 |
13 | g.101083770C>A | CA388651897 | NALCN | c.3524G>T (p.Trp1175Leu) c.3245G>T (p.Trp1082Leu) c.3611G>T (p.Trp1204Leu) c.3437G>T (p.Trp1146Leu) c.3581G>T (p.Trp1194Leu) c.3494G>T (p.Trp1165Leu) c.3302G>T (p.Trp1101Leu) c.3077G>T (p.Trp1026Leu) c.2759G>T (p.Trp920Leu) c.3668G>T (p.Trp1223Leu) | |
13 | g.101083770C>G | CA388651898 | NALCN | c.3524G>C (p.Trp1175Ser) c.3245G>C (p.Trp1082Ser) c.3611G>C (p.Trp1204Ser) c.3437G>C (p.Trp1146Ser) c.3581G>C (p.Trp1194Ser) c.3494G>C (p.Trp1165Ser) c.3302G>C (p.Trp1101Ser) c.3077G>C (p.Trp1026Ser) c.2759G>C (p.Trp920Ser) c.3668G>C (p.Trp1223Ser) | |
13 | g.101083770C>T | CA388651899 | NALCN | c.3524G>A (p.Trp1175Ter) c.3245G>A (p.Trp1082Ter) c.3611G>A (p.Trp1204Ter) c.3437G>A (p.Trp1146Ter) c.3581G>A (p.Trp1194Ter) c.3494G>A (p.Trp1165Ter) c.3302G>A (p.Trp1101Ter) c.3077G>A (p.Trp1026Ter) c.2759G>A (p.Trp920Ter) c.3668G>A (p.Trp1223Ter) | |
13 | g.101083771A>C | CA388651901 | NALCN | c.3523T>G (p.Trp1175Gly) c.3244T>G (p.Trp1082Gly) c.3610T>G (p.Trp1204Gly) c.3436T>G (p.Trp1146Gly) c.3580T>G (p.Trp1194Gly) c.3493T>G (p.Trp1165Gly) c.3301T>G (p.Trp1101Gly) c.3076T>G (p.Trp1026Gly) c.2758T>G (p.Trp920Gly) c.3667T>G (p.Trp1223Gly) | |
13 | g.101083771A>G | CA388651902 | NALCN | c.3523T>C (p.Trp1175Arg) c.3244T>C (p.Trp1082Arg) c.3610T>C (p.Trp1204Arg) c.3436T>C (p.Trp1146Arg) c.3580T>C (p.Trp1194Arg) c.3493T>C (p.Trp1165Arg) c.3301T>C (p.Trp1101Arg) c.3076T>C (p.Trp1026Arg) c.2758T>C (p.Trp920Arg) c.3667T>C (p.Trp1223Arg) | |
13 | g.101083771A>T | CA388651900 | NALCN | c.3523T>A (p.Trp1175Arg) c.3244T>A (p.Trp1082Arg) c.3610T>A (p.Trp1204Arg) c.3436T>A (p.Trp1146Arg) c.3580T>A (p.Trp1194Arg) c.3493T>A (p.Trp1165Arg) c.3301T>A (p.Trp1101Arg) c.3076T>A (p.Trp1026Arg) c.2758T>A (p.Trp920Arg) c.3667T>A (p.Trp1223Arg) | |
13 | g.101083772T>A | CA388651903 | NALCN | c.3522A>T (p.Arg1174Ser) c.3243A>T (p.Arg1081Ser) c.3609A>T (p.Arg1203Ser) c.3435A>T (p.Arg1145Ser) c.3579A>T (p.Arg1193Ser) c.3492A>T (p.Arg1164Ser) c.3300A>T (p.Arg1100Ser) c.3075A>T (p.Arg1025Ser) c.2757A>T (p.Arg919Ser) c.3666A>T (p.Arg1222Ser) | ClinVar dbSNP |
13 | g.101083772T>C | CA484553419 | NALCN | c.3522A>G (p.Arg1174=) c.3243A>G (p.Arg1081=) c.3609A>G (p.Arg1203=) c.3435A>G (p.Arg1145=) c.3579A>G (p.Arg1193=) c.3492A>G (p.Arg1164=) c.3300A>G (p.Arg1100=) c.3075A>G (p.Arg1025=) c.2757A>G (p.Arg919=) c.3666A>G (p.Arg1222=) | |
13 | g.101083772T>G | CA388651905 | NALCN | c.3522A>C (p.Arg1174Ser) c.3243A>C (p.Arg1081Ser) c.3609A>C (p.Arg1203Ser) c.3435A>C (p.Arg1145Ser) c.3579A>C (p.Arg1193Ser) c.3492A>C (p.Arg1164Ser) c.3300A>C (p.Arg1100Ser) c.3075A>C (p.Arg1025Ser) c.2757A>C (p.Arg919Ser) c.3666A>C (p.Arg1222Ser) | |
13 | g.101083772T= | CA2114389784 | NALCN | c.3522A= (p.Arg1174=) c.3243A= (p.Arg1081=) c.3609A= (p.Arg1203=) c.3435A= (p.Arg1145=) c.3579A= (p.Arg1193=) c.3492A= (p.Arg1164=) c.3300A= (p.Arg1100=) c.3075A= (p.Arg1025=) c.2757A= (p.Arg919=) c.3666A= (p.Arg1222=) | |
13 | g.101083773C>A | CA388651906 | NALCN | c.3521G>T (p.Arg1174Ile) c.3242G>T (p.Arg1081Ile) c.3608G>T (p.Arg1203Ile) c.3434G>T (p.Arg1145Ile) c.3578G>T (p.Arg1193Ile) c.3491G>T (p.Arg1164Ile) c.3299G>T (p.Arg1100Ile) c.3074G>T (p.Arg1025Ile) c.2756G>T (p.Arg919Ile) c.3665G>T (p.Arg1222Ile) | ClinVar |
13 | g.101083773C>G | CA388651908 | NALCN | c.3521G>C (p.Arg1174Thr) c.3242G>C (p.Arg1081Thr) c.3608G>C (p.Arg1203Thr) c.3434G>C (p.Arg1145Thr) c.3578G>C (p.Arg1193Thr) c.3491G>C (p.Arg1164Thr) c.3299G>C (p.Arg1100Thr) c.3074G>C (p.Arg1025Thr) c.2756G>C (p.Arg919Thr) c.3665G>C (p.Arg1222Thr) |