Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.155235708G>A | CA342712599 | GBA1 | c.1361C>T (p.Pro454Leu) c.1214C>T (p.Pro405Leu) c.1100C>T (p.Pro367Leu) n.128C>T n.352C>T n.520C>T | ClinVar gnomAD v4 |
1 | g.155235708G>C | CA253055 | GBA1 | c.1361C>G (p.Pro454Arg) c.1214C>G (p.Pro405Arg) c.1100C>G (p.Pro367Arg) n.128C>G n.352C>G n.520C>G | ClinVar dbSNP |
1 | g.155235708G= | CA1141581076 | GBA1 | c.1361C= (p.Pro454=) c.1214C= (p.Pro405=) c.1100C= (p.Pro367=) n.128C= n.352C= n.520C= | |
1 | g.155235708G>T | CA342712610 | GBA1 | c.1361C>A (p.Pro454His) c.1214C>A (p.Pro405His) c.1100C>A (p.Pro367His) n.128C>A n.352C>A n.520C>A | |
1 | g.155235709G>A | CA342712628 | GBA1 | c.1360C>T (p.Pro454Ser) c.1213C>T (p.Pro405Ser) c.1099C>T (p.Pro367Ser) n.127C>T n.351C>T n.519C>T | |
1 | g.155235709G>C | CA342712633 | GBA1 | c.1360C>G (p.Pro454Ala) c.1213C>G (p.Pro405Ala) c.1099C>G (p.Pro367Ala) n.127C>G n.351C>G n.519C>G | |
1 | g.155235709G>T | CA342712636 | GBA1 | c.1360C>A (p.Pro454Thr) c.1213C>A (p.Pro405Thr) c.1099C>A (p.Pro367Thr) n.127C>A n.351C>A n.519C>A | |
1 | g.155235710C>A | CA342712641 | GBA1 | c.1359G>T (p.Gln453His) c.1212G>T (p.Gln404His) c.1098G>T (p.Gln366His) n.126G>T n.350G>T n.518G>T | |
1 | g.155235710C>G | CA342712645 | GBA1 | c.1359G>C (p.Gln453His) c.1212G>C (p.Gln404His) c.1098G>C (p.Gln366His) n.126G>C n.350G>C n.518G>C | |
1 | g.155235710C>T | CA421020261 | GBA1 | c.1359G>A (p.Gln453=) c.1212G>A (p.Gln404=) c.1098G>A (p.Gln366=) n.126G>A n.350G>A n.518G>A | |
1 | g.155235711T>A | CA342712650 | GBA1 | c.1358A>T (p.Gln453Leu) c.1211A>T (p.Gln404Leu) c.1097A>T (p.Gln366Leu) n.125A>T n.349A>T n.517A>T | |
1 | g.155235711T>C | CA342712652 | GBA1 | c.1358A>G (p.Gln453Arg) c.1211A>G (p.Gln404Arg) c.1097A>G (p.Gln366Arg) n.125A>G n.349A>G n.517A>G | gnomAD v4 |
1 | g.155235711T>G | CA342712656 | GBA1 | c.1358A>C (p.Gln453Pro) c.1211A>C (p.Gln404Pro) c.1097A>C (p.Gln366Pro) n.125A>C n.349A>C n.517A>C | |
1 | g.155235712G>A | CA342712665 | GBA1 | c.1357C>T (p.Gln453Ter) c.1210C>T (p.Gln404Ter) c.1096C>T (p.Gln366Ter) n.124C>T n.348C>T n.516C>T | ClinVar dbSNP |
1 | g.155235712G>C | CA342712676 | GBA1 | c.1357C>G (p.Gln453Glu) c.1210C>G (p.Gln404Glu) c.1096C>G (p.Gln366Glu) n.124C>G n.348C>G n.516C>G | |
1 | g.155235712G= | CA2481201675 | GBA1 | c.1357C= (p.Gln453=) c.1210C= (p.Gln404=) c.1096C= (p.Gln366=) n.124C= n.348C= n.516C= | |
1 | g.155235712G>T | CA342712685 | GBA1 | c.1357C>A (p.Gln453Lys) c.1210C>A (p.Gln404Lys) c.1096C>A (p.Gln366Lys) n.124C>A n.348C>A n.516C>A | |
1 | g.155235713T>A | CA342712709 | GBA1 | c.1356A>T (p.Lys452Asn) c.1209A>T (p.Lys403Asn) c.1095A>T (p.Lys365Asn) n.123A>T n.347A>T n.515A>T | |
1 | g.155235713T>C | CA421020265 | GBA1 | c.1356A>G (p.Lys452=) c.1209A>G (p.Lys403=) c.1095A>G (p.Lys365=) n.123A>G n.347A>G n.515A>G | |
1 | g.155235713T>G | CA342712717 | GBA1 | c.1356A>C (p.Lys452Asn) c.1209A>C (p.Lys403Asn) c.1095A>C (p.Lys365Asn) n.123A>C n.347A>C n.515A>C | |
1 | g.155235714T>A | CA342712721 | GBA1 | c.1355A>T (p.Lys452Ile) c.1208A>T (p.Lys403Ile) c.1094A>T (p.Lys365Ile) n.122A>T n.346A>T n.514A>T | |
1 | g.155235714T>C | CA342712722 | GBA1 | c.1355A>G (p.Lys452Arg) c.1208A>G (p.Lys403Arg) c.1094A>G (p.Lys365Arg) n.122A>G n.346A>G n.514A>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
1 | g.155235714T>G | CA342712723 | GBA1 | c.1355A>C (p.Lys452Thr) c.1208A>C (p.Lys403Thr) c.1094A>C (p.Lys365Thr) n.122A>C n.346A>C n.514A>C | |
1 | g.155235714T= | CA2481201676 | GBA1 | c.1355A= (p.Lys452=) c.1208A= (p.Lys403=) c.1094A= (p.Lys365=) n.122A= n.346A= n.514A= | |
1 | g.155235714_155235716delinsTTG | CA2481201677 | GBA1 | c.1353_1355delinsCAA (p.Tyr451=) c.1206_1208delinsCAA (p.Tyr402=) c.1092_1094delinsCAA (p.Tyr364=) n.120_122delinsCAA n.344_346delinsCAA n.512_514delinsCAA | |
1 | g.155235715T>A | CA342712724 | GBA1 | c.1354A>T (p.Lys452Ter) c.1207A>T (p.Lys403Ter) c.1093A>T (p.Lys365Ter) n.121A>T n.345A>T n.513A>T | |
1 | g.155235715T>C | CA342712725 | GBA1 | c.1354A>G (p.Lys452Glu) c.1207A>G (p.Lys403Glu) c.1093A>G (p.Lys365Glu) n.121A>G n.345A>G n.513A>G | |
1 | g.155235715T>G | CA342712729 | GBA1 | c.1354A>C (p.Lys452Gln) c.1207A>C (p.Lys403Gln) c.1093A>C (p.Lys365Gln) n.121A>C n.345A>C n.513A>C | dbSNP |
1 | g.155235716_155235717del | CA1007991463 | GBA1 | c.1353_1354del (p.Tyr451Ter) c.1206_1207del (p.Tyr402Ter) c.1092_1093del (p.Tyr364Ter) n.120_121del n.344_345del n.512_513del | dbSNP gnomAD v3 gnomAD v4 |
1 | g.155235716G>A | CA30894454 | GBA1 | c.1353C>T (p.Tyr451=) c.1206C>T (p.Tyr402=) c.1092C>T (p.Tyr364=) n.120C>T n.344C>T n.512C>T | dbSNP gnomAD v2 gnomAD v4 |
1 | g.155235716G>C | CA342712739 | GBA1 | c.1353C>G (p.Tyr451Ter) c.1206C>G (p.Tyr402Ter) c.1092C>G (p.Tyr364Ter) n.120C>G n.344C>G n.512C>G | |
1 | g.155235716G= | CA1141088621 | GBA1 | c.1353C= (p.Tyr451=) c.1206C= (p.Tyr402=) c.1092C= (p.Tyr364=) n.120C= n.344C= n.512C= | |
1 | g.155235716G>T | CA342712744 | GBA1 | c.1353C>A (p.Tyr451Ter) c.1206C>A (p.Tyr402Ter) c.1092C>A (p.Tyr364Ter) n.120C>A n.344C>A n.512C>A | |
1 | g.155235717T>A | CA342712749 | GBA1 | c.1352A>T (p.Tyr451Phe) c.1205A>T (p.Tyr402Phe) c.1091A>T (p.Tyr364Phe) n.119A>T n.343A>T n.511A>T | |
1 | g.155235717T>C | CA342712751 | GBA1 | c.1352A>G (p.Tyr451Cys) c.1205A>G (p.Tyr402Cys) c.1091A>G (p.Tyr364Cys) n.119A>G n.343A>G n.511A>G | |
1 | g.155235717T>G | CA342712752 | GBA1 | c.1352A>C (p.Tyr451Ser) c.1205A>C (p.Tyr402Ser) c.1091A>C (p.Tyr364Ser) n.119A>C n.343A>C n.511A>C | |
1 | g.155235718A>C | CA342712754 | GBA1 | c.1351T>G (p.Tyr451Asp) c.1204T>G (p.Tyr402Asp) c.1090T>G (p.Tyr364Asp) n.118T>G n.342T>G n.510T>G | |
1 | g.155235718A>G | CA342712756 | GBA1 | c.1351T>C (p.Tyr451His) c.1204T>C (p.Tyr402His) c.1090T>C (p.Tyr364His) n.118T>C n.342T>C n.510T>C | |
1 | g.155235718A>T | CA342712753 | GBA1 | c.1351T>A (p.Tyr451Asn) c.1204T>A (p.Tyr402Asn) c.1090T>A (p.Tyr364Asn) n.118T>A n.342T>A n.510T>A | |
1 | g.155235719A= | CA1141023013 | GBA1 | c.1350T= (p.Phe450=) c.1203T= (p.Phe401=) c.1089T= (p.Phe363=) n.117T= n.341T= n.509T= | |
1 | g.155235719A>C | CA342712757 | GBA1 | c.1350T>G (p.Phe450Leu) c.1203T>G (p.Phe401Leu) c.1089T>G (p.Phe363Leu) n.117T>G n.341T>G n.509T>G | |
1 | g.155235719A>G | CA421020273 | GBA1 | c.1350T>C (p.Phe450=) c.1203T>C (p.Phe401=) c.1089T>C (p.Phe363=) n.117T>C n.341T>C n.509T>C | |
1 | g.155235719A>T | CA30894455 | GBA1 | c.1350T>A (p.Phe450Leu) c.1203T>A (p.Phe401Leu) c.1089T>A (p.Phe363Leu) n.117T>A n.341T>A n.509T>A | dbSNP |
1 | g.155235720A>C | CA342712783 | GBA1 | c.1349T>G (p.Phe450Cys) c.1202T>G (p.Phe401Cys) c.1088T>G (p.Phe363Cys) n.116T>G n.340T>G n.508T>G | |
1 | g.155235720A>G | CA342712789 | GBA1 | c.1349T>C (p.Phe450Ser) c.1202T>C (p.Phe401Ser) c.1088T>C (p.Phe363Ser) n.116T>C n.340T>C n.508T>C | |
1 | g.155235720A>T | CA342712790 | GBA1 | c.1349T>A (p.Phe450Tyr) c.1202T>A (p.Phe401Tyr) c.1088T>A (p.Phe363Tyr) n.116T>A n.340T>A n.508T>A | |
1 | g.155235721A= | CA2481201678 | GBA1 | c.1348T= (p.Phe450=) c.1201T= (p.Phe401=) c.1087T= (p.Phe363=) n.115T= n.339T= n.507T= | |
1 | g.155235721A>C | CA342712793 | GBA1 | c.1348T>G (p.Phe450Val) c.1201T>G (p.Phe401Val) c.1087T>G (p.Phe363Val) n.115T>G n.339T>G n.507T>G | |
1 | g.155235721A>G | CA342712791 | GBA1 | c.1348T>C (p.Phe450Leu) c.1201T>C (p.Phe401Leu) c.1087T>C (p.Phe363Leu) n.115T>C n.339T>C n.507T>C | |
1 | g.155235721A>T | CA342712792 | GBA1 | c.1348T>A (p.Phe450Ile) c.1201T>A (p.Phe401Ile) c.1087T>A (p.Phe363Ile) n.115T>A n.339T>A n.507T>A | ClinVar dbSNP |
1 | g.155235722C>A | CA421020275 | GBA1 | c.1347G>T (p.Thr449=) c.1200G>T (p.Thr400=) c.1086G>T (p.Thr362=) n.114G>T n.338G>T n.506G>T | |
1 | g.155235722C= | CA2481201679 | GBA1 | c.1347G= (p.Thr449=) c.1200G= (p.Thr400=) c.1086G= (p.Thr362=) n.114G= n.338G= n.506G= | |
1 | g.155235722C>G | CA1141550 | GBA1 | c.1347G>C (p.Thr449=) c.1200G>C (p.Thr400=) c.1086G>C (p.Thr362=) n.114G>C n.338G>C n.506G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.155235722C>T | CA1141551 | GBA1 | c.1347G>A (p.Thr449=) c.1200G>A (p.Thr400=) c.1086G>A (p.Thr362=) n.114G>A n.338G>A n.506G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.155235723G>A | CA1141552 | GBA1 | c.1346C>T (p.Thr449Met) c.1199C>T (p.Thr400Met) c.1085C>T (p.Thr362Met) n.113C>T n.337C>T n.505C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.155235723G>C | CA342712819 | GBA1 | c.1346C>G (p.Thr449Arg) c.1199C>G (p.Thr400Arg) c.1085C>G (p.Thr362Arg) n.113C>G n.337C>G n.505C>G | dbSNP gnomAD v4 |
1 | g.155235723G= | CA2481201680 | GBA1 | c.1346C= (p.Thr449=) c.1199C= (p.Thr400=) c.1085C= (p.Thr362=) n.113C= n.337C= n.505C= | |
1 | g.155235723G>T | CA342712825 | GBA1 | c.1346C>A (p.Thr449Lys) c.1199C>A (p.Thr400Lys) c.1085C>A (p.Thr362Lys) n.113C>A n.337C>A n.505C>A | |
1 | g.155235724T>A | CA342712831 | GBA1 | c.1345A>T (p.Thr449Ser) c.1198A>T (p.Thr400Ser) c.1084A>T (p.Thr362Ser) n.112A>T n.336A>T n.504A>T | |
1 | g.155235724T>C | CA342712841 | GBA1 | c.1345A>G (p.Thr449Ala) c.1198A>G (p.Thr400Ala) c.1084A>G (p.Thr362Ala) n.112A>G n.336A>G n.504A>G | gnomAD v4 |
1 | g.155235724T>G | CA342712834 | GBA1 | c.1345A>C (p.Thr449Pro) c.1198A>C (p.Thr400Pro) c.1084A>C (p.Thr362Pro) n.112A>C n.336A>C n.504A>C | |
1 | g.155235725G>A | CA421020276 | GBA1 | c.1344C>T (p.Asp448=) c.1197C>T (p.Asp399=) c.1083C>T (p.Asp361=) n.111C>T n.335C>T n.503C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.155235725G>C | CA1141553 | GBA1 | c.1344C>G (p.Asp448Glu) c.1197C>G (p.Asp399Glu) c.1083C>G (p.Asp361Glu) n.111C>G n.335C>G n.503C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.155235725G= | CA1141110513 | GBA1 | c.1344C= (p.Asp448=) c.1197C= (p.Asp399=) c.1083C= (p.Asp361=) n.111C= n.335C= n.503C= | |
1 | g.155235725G>T | CA342712846 | GBA1 | c.1344C>A (p.Asp448Glu) c.1197C>A (p.Asp399Glu) c.1083C>A (p.Asp361Glu) n.111C>A n.335C>A n.503C>A | |
1 | g.155235726T>A | CA253061 | GBA1 | c.1343A>T (p.Asp448Val) c.1196A>T (p.Asp399Val) c.1082A>T (p.Asp361Val) n.110A>T n.334A>T n.502A>T | ClinVar dbSNP |
1 | g.155235726T>C | CA342712861 | GBA1 | c.1343A>G (p.Asp448Gly) c.1196A>G (p.Asp399Gly) c.1082A>G (p.Asp361Gly) n.110A>G n.334A>G n.502A>G | |
1 | g.155235726T>G | CA342712867 | GBA1 | c.1343A>C (p.Asp448Ala) c.1196A>C (p.Asp399Ala) c.1082A>C (p.Asp361Ala) n.110A>C n.334A>C n.502A>C | |
1 | g.155235726T= | CA1141039915 | GBA1 | c.1343A= (p.Asp448=) c.1196A= (p.Asp399=) c.1082A= (p.Asp361=) n.110A= n.334A= n.502A= | |
1 | g.155235727C>A | CA342712871 | GBA1 | c.1342G>T (p.Asp448Tyr) c.1195G>T (p.Asp399Tyr) c.1081G>T (p.Asp361Tyr) n.109G>T n.333G>T n.501G>T | |
1 | g.155235727C= | CA1139849879 | GBA1 | c.1342G= (p.Asp448=) c.1195G= (p.Asp399=) c.1081G= (p.Asp361=) n.109G= n.333G= n.501G= | |
1 | g.155235727C>G | CA221392 | GBA1 | c.1342G>C (p.Asp448His) c.1195G>C (p.Asp399His) c.1081G>C (p.Asp361His) n.109G>C n.333G>C n.501G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.[155235727C>G;155237458A>C] | CA028618 | GBA1 | c.[882T>G;1342G>C] (p.[His294Gln;Asp448His]) c.[735T>G;1195G>C] (p.[His245Gln;Asp399His]) c.[621T>G;1081G>C] (p.[His207Gln;Asp361His]) n.[340-1170T>G;501G>C] | |
1 | g.155235727C>T | CA342712884 | GBA1 | c.1342G>A (p.Asp448Asn) c.1195G>A (p.Asp399Asn) c.1081G>A (p.Asp361Asn) n.109G>A n.333G>A n.501G>A | gnomAD v4 |
1 | g.155235728C>A | CA342712887 | GBA1 | c.1341G>T (p.Lys447Asn) c.1194G>T (p.Lys398Asn) c.1080G>T (p.Lys360Asn) n.108G>T n.332G>T n.500G>T | |
1 | g.155235728C>G | CA342712889 | GBA1 | c.1341G>C (p.Lys447Asn) c.1194G>C (p.Lys398Asn) c.1080G>C (p.Lys360Asn) n.108G>C n.332G>C n.500G>C | |
1 | g.155235728C>T | CA421020277 | GBA1 | c.1341G>A (p.Lys447=) c.1194G>A (p.Lys398=) c.1080G>A (p.Lys360=) n.108G>A n.332G>A n.500G>A | |
1 | g.155235729T>A | CA342712895 | GBA1 | c.1340A>T (p.Lys447Met) c.1193A>T (p.Lys398Met) c.1079A>T (p.Lys360Met) n.107A>T n.331A>T n.499A>T | |
1 | g.155235729T>C | CA342712898 | GBA1 | c.1340A>G (p.Lys447Arg) c.1193A>G (p.Lys398Arg) c.1079A>G (p.Lys360Arg) n.107A>G n.331A>G n.499A>G | dbSNP |
1 | g.155235729T>G | CA342712901 | GBA1 | c.1340A>C (p.Lys447Thr) c.1193A>C (p.Lys398Thr) c.1079A>C (p.Lys360Thr) n.107A>C n.331A>C n.499A>C | |
1 | g.155235729T= | CA2481201681 | GBA1 | c.1340A= (p.Lys447=) c.1193A= (p.Lys398=) c.1079A= (p.Lys360=) n.107A= n.331A= n.499A= | |
1 | g.155235730T>A | CA342712907 | GBA1 | c.1339A>T (p.Lys447Ter) c.1192A>T (p.Lys398Ter) c.1078A>T (p.Lys360Ter) n.106A>T n.330A>T n.498A>T | |
1 | g.155235730T>C | CA342712906 | GBA1 | c.1339A>G (p.Lys447Glu) c.1192A>G (p.Lys398Glu) c.1078A>G (p.Lys360Glu) n.106A>G n.330A>G n.498A>G | |
1 | g.155235730T>G | CA342712905 | GBA1 | c.1339A>C (p.Lys447Gln) c.1192A>C (p.Lys398Gln) c.1078A>C (p.Lys360Gln) n.106A>C n.330A>C n.498A>C | |
1 | g.155235731G>A | CA421020282 | GBA1 | c.1338C>T (p.Thr446=) c.1191C>T (p.Thr397=) c.1077C>T (p.Thr359=) n.105C>T n.329C>T n.497C>T | dbSNP gnomAD v2 |
1 | g.155235731G>C | CA421020281 | GBA1 | c.1338C>G (p.Thr446=) c.1191C>G (p.Thr397=) c.1077C>G (p.Thr359=) n.105C>G n.329C>G n.497C>G | |
1 | g.155235731G= | CA2481201682 | GBA1 | c.1338C= (p.Thr446=) c.1191C= (p.Thr397=) c.1077C= (p.Thr359=) n.105C= n.329C= n.497C= | |
1 | g.155235731G>T | CA421020280 | GBA1 | c.1338C>A (p.Thr446=) c.1191C>A (p.Thr397=) c.1077C>A (p.Thr359=) n.105C>A n.329C>A n.497C>A | |
1 | g.155235732G>A | CA342712908 | GBA1 | c.1337C>T (p.Thr446Ile) c.1190C>T (p.Thr397Ile) c.1076C>T (p.Thr359Ile) n.104C>T n.328C>T n.496C>T | |
1 | g.155235732G>C | CA342712909 | GBA1 | c.1337C>G (p.Thr446Ser) c.1190C>G (p.Thr397Ser) c.1076C>G (p.Thr359Ser) n.104C>G n.328C>G n.496C>G | |
1 | g.155235732G= | CA1143534667 | GBA1 | c.1337C= (p.Thr446=) c.1190C= (p.Thr397=) c.1076C= (p.Thr359=) n.104C= n.328C= n.496C= | |
1 | g.155235732G>T | CA30894467 | GBA1 | c.1337C>A (p.Thr446Asn) c.1190C>A (p.Thr397Asn) c.1076C>A (p.Thr359Asn) n.104C>A n.328C>A n.496C>A | dbSNP |
1 | g.155235733T>A | CA342712910 | GBA1 | c.1336A>T (p.Thr446Ser) c.1189A>T (p.Thr397Ser) c.1075A>T (p.Thr359Ser) n.103A>T n.327A>T n.495A>T | |
1 | g.155235733T>C | CA342712915 | GBA1 | c.1336A>G (p.Thr446Ala) c.1189A>G (p.Thr397Ala) c.1075A>G (p.Thr359Ala) n.103A>G n.327A>G n.495A>G | |
1 | g.155235733T>G | CA342712920 | GBA1 | c.1336A>C (p.Thr446Pro) c.1189A>C (p.Thr397Pro) c.1075A>C (p.Thr359Pro) n.103A>C n.327A>C n.495A>C | |
1 | g.155235734G>A | CA421020286 | GBA1 | c.1335C>T (p.Ile445=) c.1188C>T (p.Ile396=) c.1074C>T (p.Ile358=) n.102C>T n.326C>T n.494C>T | |
1 | g.155235734G>C | CA342712924 | GBA1 | c.1335C>G (p.Ile445Met) c.1188C>G (p.Ile396Met) c.1074C>G (p.Ile358Met) n.102C>G n.326C>G n.494C>G | |
1 | g.155235734G>T | CA421020287 | GBA1 | c.1335C>A (p.Ile445=) c.1188C>A (p.Ile396=) c.1074C>A (p.Ile358=) n.102C>A n.326C>A n.494C>A | |
1 | g.155235735A>C | CA342712927 | GBA1 | c.1334T>G (p.Ile445Ser) c.1187T>G (p.Ile396Ser) c.1073T>G (p.Ile358Ser) n.101T>G n.325T>G n.493T>G | |
1 | g.155235735A>G | CA342712933 | GBA1 | c.1334T>C (p.Ile445Thr) c.1187T>C (p.Ile396Thr) c.1073T>C (p.Ile358Thr) n.101T>C n.325T>C n.493T>C | |
1 | g.155235735A>T | CA342712934 | GBA1 | c.1334T>A (p.Ile445Asn) c.1187T>A (p.Ile396Asn) c.1073T>A (p.Ile358Asn) n.101T>A n.325T>A n.493T>A | |
1 | g.155235736T>A | CA342712939 | GBA1 | c.1333A>T (p.Ile445Phe) c.1186A>T (p.Ile396Phe) c.1072A>T (p.Ile358Phe) n.100A>T n.324A>T n.492A>T | |
1 | g.155235736T>C | CA342712950 | GBA1 | c.1333A>G (p.Ile445Val) c.1186A>G (p.Ile396Val) c.1072A>G (p.Ile358Val) n.100A>G n.324A>G n.492A>G | gnomAD v4 |
1 | g.155235736T>G | CA342712952 | GBA1 | c.1333A>C (p.Ile445Leu) c.1186A>C (p.Ile396Leu) c.1072A>C (p.Ile358Leu) n.100A>C n.324A>C n.492A>C | |
1 | g.155235737G>A | CA1141554 | GBA1 | c.1332C>T (p.Asp444=) c.1185C>T (p.Asp395=) c.1071C>T (p.Asp357=) n.99C>T n.323C>T n.491C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.155235737G>C | CA342712964 | GBA1 | c.1332C>G (p.Asp444Glu) c.1185C>G (p.Asp395Glu) c.1071C>G (p.Asp357Glu) n.99C>G n.323C>G n.491C>G | |
1 | g.155235737G= | CA2481201683 | GBA1 | c.1332C= (p.Asp444=) c.1185C= (p.Asp395=) c.1071C= (p.Asp357=) n.99C= n.323C= n.491C= | |
1 | g.155235737G>T | CA342712962 | GBA1 | c.1332C>A (p.Asp444Glu) c.1185C>A (p.Asp395Glu) c.1071C>A (p.Asp357Glu) n.99C>A n.323C>A n.491C>A | |
1 | g.155235738T>A | CA342712987 | GBA1 | c.1331A>T (p.Asp444Val) c.1184A>T (p.Asp395Val) c.1070A>T (p.Asp357Val) n.98A>T n.322A>T n.490A>T | gnomAD v4 |
1 | g.155235738T>C | CA342712981 | GBA1 | c.1331A>G (p.Asp444Gly) c.1184A>G (p.Asp395Gly) c.1070A>G (p.Asp357Gly) n.98A>G n.322A>G n.490A>G | |
1 | g.155235738T>G | CA342712984 | GBA1 | c.1331A>C (p.Asp444Ala) c.1184A>C (p.Asp395Ala) c.1070A>C (p.Asp357Ala) n.98A>C n.322A>C n.490A>C | |
1 | g.155235739C>A | CA342712992 | GBA1 | c.1330G>T (p.Asp444Tyr) c.1183G>T (p.Asp395Tyr) c.1069G>T (p.Asp357Tyr) n.97G>T n.321G>T n.489G>T | |
1 | g.155235739C>G | CA342712993 | GBA1 | c.1330G>C (p.Asp444His) c.1183G>C (p.Asp395His) c.1069G>C (p.Asp357His) n.97G>C n.321G>C n.489G>C | |
1 | g.155235739C>T | CA342712994 | GBA1 | c.1330G>A (p.Asp444Asn) c.1183G>A (p.Asp395Asn) c.1069G>A (p.Asp357Asn) n.97G>A n.321G>A n.489G>A | |
1 | g.155235740T>A | CA421020289 | GBA1 | c.1329A>T (p.Val443=) c.1182A>T (p.Val394=) c.1068A>T (p.Val356=) n.96A>T n.320A>T n.488A>T | |
1 | g.155235740T>C | CA421020290 | GBA1 | c.1329A>G (p.Val443=) c.1182A>G (p.Val394=) c.1068A>G (p.Val356=) n.96A>G n.320A>G n.488A>G | |
1 | g.155235740T>G | CA421020291 | GBA1 | c.1329A>C (p.Val443=) c.1182A>C (p.Val394=) c.1068A>C (p.Val356=) n.96A>C n.320A>C n.488A>C | |
1 | g.155235741A>C | CA342712995 | GBA1 | c.1328T>G (p.Val443Gly) c.1181T>G (p.Val394Gly) c.1067T>G (p.Val356Gly) n.95T>G n.319T>G n.487T>G | |
1 | g.155235741A>G | CA342712996 | GBA1 | c.1328T>C (p.Val443Ala) c.1181T>C (p.Val394Ala) c.1067T>C (p.Val356Ala) n.95T>C n.319T>C n.487T>C | |
1 | g.155235741A>T | CA342712999 | GBA1 | c.1328T>A (p.Val443Glu) c.1181T>A (p.Val394Glu) c.1067T>A (p.Val356Glu) n.95T>A n.319T>A n.487T>A | |
1 | g.155235742C>A | CA342713003 | GBA1 | c.1327G>T (p.Val443Leu) c.1180G>T (p.Val394Leu) c.1066G>T (p.Val356Leu) n.94G>T n.318G>T n.486G>T | |
1 | g.155235742C>G | CA342713006 | GBA1 | c.1327G>C (p.Val443Leu) c.1180G>C (p.Val394Leu) c.1066G>C (p.Val356Leu) n.94G>C n.318G>C n.486G>C | |
1 | g.155235742C>T | CA342713010 | GBA1 | c.1327G>A (p.Val443Ile) c.1180G>A (p.Val394Ile) c.1066G>A (p.Val356Ile) n.94G>A n.318G>A n.486G>A | |
1 | g.155235742_155235745delinsCAAT | CA2481201684 | GBA1 | c.1324_1327delinsATTG (p.Ile442=) c.1177_1180delinsATTG (p.Ile393=) c.1063_1066delinsATTG (p.Ile355=) n.91_94delinsATTG n.315_318delinsATTG n.483_486delinsATTG | |
1 | g.155235743A>C | CA342713021 | GBA1 | c.1326T>G (p.Ile442Met) c.1179T>G (p.Ile393Met) c.1065T>G (p.Ile355Met) n.93T>G n.317T>G n.485T>G | |
1 | g.155235743A>G | CA421020294 | GBA1 | c.1326T>C (p.Ile442=) c.1179T>C (p.Ile393=) c.1065T>C (p.Ile355=) n.93T>C n.317T>C n.485T>C | |
1 | g.155235743A>T | CA421020295 | GBA1 | c.1326T>A (p.Ile442=) c.1179T>A (p.Ile393=) c.1065T>A (p.Ile355=) n.93T>A n.317T>A n.485T>A | |
1 | g.155235744dup | CA2586967439 | GBA1 | c.1326dup (p.Val443CysfsTer26) c.1179dup (p.Val394CysfsTer26) c.1065dup (p.Val356CysfsTer26) n.93dup n.317dup n.485dup | |
1 | g.155235743_155235745del | CA2481201685 | GBA1 | c.1324_1326del (p.Ile442del) c.1177_1179del (p.Ile393del) c.1063_1065del (p.Ile355del) n.91_93del n.315_317del n.483_485del | dbSNP |
1 | g.155235744A= | CA2481201686 | GBA1 | c.1325T= (p.Ile442=) c.1178T= (p.Ile393=) c.1064T= (p.Ile355=) n.92T= n.316T= n.484T= | |
1 | g.155235744A>C | CA342713034 | GBA1 | c.1325T>G (p.Ile442Ser) c.1178T>G (p.Ile393Ser) c.1064T>G (p.Ile355Ser) n.92T>G n.316T>G n.484T>G | |
1 | g.155235744A>G | CA342713036 | GBA1 | c.1325T>C (p.Ile442Thr) c.1178T>C (p.Ile393Thr) c.1064T>C (p.Ile355Thr) n.92T>C n.316T>C n.484T>C | dbSNP gnomAD v2 gnomAD v4 |
1 | g.155235744A>T | CA342713028 | GBA1 | c.1325T>A (p.Ile442Asn) c.1178T>A (p.Ile393Asn) c.1064T>A (p.Ile355Asn) n.92T>A n.316T>A n.484T>A | |
1 | g.155235745T>A | CA342713039 | GBA1 | c.1324A>T (p.Ile442Phe) c.1177A>T (p.Ile393Phe) c.1063A>T (p.Ile355Phe) n.91A>T n.315A>T n.483A>T | |
1 | g.155235745T>C | CA342713043 | GBA1 | c.1324A>G (p.Ile442Val) c.1177A>G (p.Ile393Val) c.1063A>G (p.Ile355Val) n.91A>G n.315A>G n.483A>G | |
1 | g.155235745T>G | CA342713049 | GBA1 | c.1324A>C (p.Ile442Leu) c.1177A>C (p.Ile393Leu) c.1063A>C (p.Ile355Leu) n.91A>C n.315A>C n.483A>C | |
1 | g.155235746G>A | CA421020300 | GBA1 | c.1323C>T (p.Ile441=) c.1176C>T (p.Ile392=) c.1062C>T (p.Ile354=) n.90C>T n.314C>T n.482C>T | |
1 | g.155235746G>C | CA30894468 | GBA1 | c.1323C>G (p.Ile441Met) c.1176C>G (p.Ile392Met) c.1062C>G (p.Ile354Met) n.90C>G n.314C>G n.482C>G | dbSNP gnomAD v4 |
1 | g.155235746G= | CA2481201687 | GBA1 | c.1323C= (p.Ile441=) c.1176C= (p.Ile392=) c.1062C= (p.Ile354=) n.90C= n.314C= n.482C= | |
1 | g.155235746G>T | CA421020301 | GBA1 | c.1323C>A (p.Ile441=) c.1176C>A (p.Ile392=) c.1062C>A (p.Ile354=) n.90C>A n.314C>A n.482C>A | gnomAD v4 |
1 | g.155235747A= | CA1140949629 | GBA1 | c.1322T= (p.Ile441=) c.1175T= (p.Ile392=) c.1061T= (p.Ile354=) n.89T= n.313T= n.481T= | |
1 | g.155235747A>C | CA342713096 | GBA1 | c.1322T>G (p.Ile441Ser) c.1175T>G (p.Ile392Ser) c.1061T>G (p.Ile354Ser) n.89T>G n.313T>G n.481T>G | gnomAD v4 |
1 | g.155235747A>G | CA30894469 | GBA1 | c.1322T>C (p.Ile441Thr) c.1175T>C (p.Ile392Thr) c.1061T>C (p.Ile354Thr) n.89T>C n.313T>C n.481T>C | dbSNP gnomAD v4 |
1 | g.155235747A>T | CA342713079 | GBA1 | c.1322T>A (p.Ile441Asn) c.1175T>A (p.Ile392Asn) c.1061T>A (p.Ile354Asn) n.89T>A n.313T>A n.481T>A | |
1 | g.155235748T>A | CA342713104 | GBA1 | c.1321A>T (p.Ile441Phe) c.1174A>T (p.Ile392Phe) c.1060A>T (p.Ile354Phe) n.88A>T n.312A>T n.480A>T | gnomAD v4 |
1 | g.155235748T>C | CA342713107 | GBA1 | c.1321A>G (p.Ile441Val) c.1174A>G (p.Ile392Val) c.1060A>G (p.Ile354Val) n.88A>G n.312A>G n.480A>G | |
1 | g.155235748T>G | CA342713113 | GBA1 | c.1321A>C (p.Ile441Leu) c.1174A>C (p.Ile392Leu) c.1060A>C (p.Ile354Leu) n.88A>C n.312A>C n.480A>C | |
1 | g.155235749G>A | CA421020308 | GBA1 | c.1320C>T (p.Pro440=) c.1173C>T (p.Pro391=) c.1059C>T (p.Pro353=) n.87C>T n.311C>T n.479C>T | dbSNP gnomAD v4 COSMIC |
1 | g.155235749G>C | CA421020305 | GBA1 | c.1320C>G (p.Pro440=) c.1173C>G (p.Pro391=) c.1059C>G (p.Pro353=) n.87C>G n.311C>G n.479C>G | |
1 | g.155235749G= | CA2481201689 | GBA1 | c.1320C= (p.Pro440=) c.1173C= (p.Pro391=) c.1059C= (p.Pro353=) n.87C= n.311C= n.479C= | |
1 | g.155235749G>T | CA421020307 | GBA1 | c.1320C>A (p.Pro440=) c.1173C>A (p.Pro391=) c.1059C>A (p.Pro353=) n.87C>A n.311C>A n.479C>A | |
1 | g.155235749_155235804delinsGGGACTGTCGACAAAGTTACGCACCCAATTGGGTCCTCCTTCGGGGTTCAGGGCAA | CA2481201688 | GBA1 | c.1265_1320delinsTTGCCCTGAACCCCGAAGGAGGACCCAATTGGGTGCGTAACTTTGTCGACAGTCCC (p.Leu422=) c.1118_1173delinsTTGCCCTGAACCCCGAAGGAGGACCCAATTGGGTGCGTAACTTTGTCGACAGTCCC (p.Leu373=) c.1004_1059delinsTTGCCCTGAACCCCGAAGGAGGACCCAATTGGGTGCGTAACTTTGTCGACAGTCCC (p.Leu335=) n.32_87delinsTTGCCCTGAACCCCGAAGGAGGACCCAATTGGGTGCGTAACTTTGTCGACAGTCCC n.256_311delinsTTGCCCTGAACCCCGAAGGAGGACCCAATTGGGTGCGTAACTTTGTCGACAGTCCC n.424_479delinsTTGCCCTGAACCCCGAAGGAGGACCCAATTGGGTGCGTAACTTTGTCGACAGTCCC | |
1 | g.155235751_155235806del | CA2573051379 | GBA1 | c.1265_1320del (p.Leu422HisfsTer28) c.1118_1173del (p.Leu373HisfsTer28) c.1004_1059del (p.Leu335HisfsTer28) n.32_87del n.256_311del n.424_479del | ClinVar dbSNP |
1 | g.155235750G>A | CA253103 | GBA1 | c.1319C>T (p.Pro440Leu) c.1172C>T (p.Pro391Leu) c.1058C>T (p.Pro353Leu) n.86C>T n.310C>T n.478C>T | ClinVar dbSNP COSMIC |
1 | g.155235750G>C | CA342713122 | GBA1 | c.1319C>G (p.Pro440Arg) c.1172C>G (p.Pro391Arg) c.1058C>G (p.Pro353Arg) n.86C>G n.310C>G n.478C>G | |
1 | g.155235750G= | CA1140900752 | GBA1 | c.1319C= (p.Pro440=) c.1172C= (p.Pro391=) c.1058C= (p.Pro353=) n.86C= n.310C= n.478C= | |
1 | g.155235750G>T | CA342713128 | GBA1 | c.1319C>A (p.Pro440His) c.1172C>A (p.Pro391His) c.1058C>A (p.Pro353His) n.86C>A n.310C>A n.478C>A | |
1 | g.155235750_155235806delinsGGACTGTCGACAAAGTTACGCACCCAATTGGGTCCTCCTTCGGGGTTCAGGGCAAGG | CA1141188037 | GBA1 | c.1263_1319delinsCCTTGCCCTGAACCCCGAAGGAGGACCCAATTGGGTGCGTAACTTTGTCGACAGTCC (p.Asn421=) c.1116_1172delinsCCTTGCCCTGAACCCCGAAGGAGGACCCAATTGGGTGCGTAACTTTGTCGACAGTCC (p.Asn372=) c.1002_1058delinsCCTTGCCCTGAACCCCGAAGGAGGACCCAATTGGGTGCGTAACTTTGTCGACAGTCC (p.Asn334=) n.30_86delinsCCTTGCCCTGAACCCCGAAGGAGGACCCAATTGGGTGCGTAACTTTGTCGACAGTCC n.254_310delinsCCTTGCCCTGAACCCCGAAGGAGGACCCAATTGGGTGCGTAACTTTGTCGACAGTCC n.422_478delinsCCTTGCCCTGAACCCCGAAGGAGGACCCAATTGGGTGCGTAACTTTGTCGACAGTCC | |
1 | g.155235752_155235806del | CA253083 | GBA1 | c.1265_1319del (p.Leu422ProfsTer4) c.1118_1172del (p.Leu373ProfsTer4) c.1004_1058del (p.Leu335ProfsTer4) n.32_86del n.256_310del n.424_478del | ClinVar dbSNP |
1 | g.155235752_155235833del | CA2586967440 | GBA1 | c.1238_1319del (p.His413ProfsTer4) c.1091_1172del (p.His364ProfsTer4) c.977_1058del (p.His326ProfsTer4) n.5_86del n.229_310del n.397_478del | |
1 | g.155235751G>A | CA1141555 | GBA1 | c.1318C>T (p.Pro440Ser) c.1171C>T (p.Pro391Ser) c.1057C>T (p.Pro353Ser) n.85C>T n.309C>T n.477C>T | dbSNP ExAC gnomAD v2 |
1 | g.155235751G>C | CA342713139 | GBA1 | c.1318C>G (p.Pro440Ala) c.1171C>G (p.Pro391Ala) c.1057C>G (p.Pro353Ala) n.85C>G n.309C>G n.477C>G | |
1 | g.155235751G= | CA2481201690 | GBA1 | c.1318C= (p.Pro440=) c.1171C= (p.Pro391=) c.1057C= (p.Pro353=) n.85C= n.309C= n.477C= | |
1 | g.155235751G>T | CA342713136 | GBA1 | c.1318C>A (p.Pro440Thr) c.1171C>A (p.Pro391Thr) c.1057C>A (p.Pro353Thr) n.85C>A n.309C>A n.477C>A | |
1 | g.155235752A>C | CA342713141 | GBA1 | c.1317T>G (p.Ser439Arg) c.1170T>G (p.Ser390Arg) c.1056T>G (p.Ser352Arg) n.84T>G n.308T>G n.476T>G | |
1 | g.155235752A>G | CA421020310 | GBA1 | c.1317T>C (p.Ser439=) c.1170T>C (p.Ser390=) c.1056T>C (p.Ser352=) n.84T>C n.308T>C n.476T>C | gnomAD v4 |
1 | g.155235752A>T | CA342713143 | GBA1 | c.1317T>A (p.Ser439Arg) c.1170T>A (p.Ser390Arg) c.1056T>A (p.Ser352Arg) n.84T>A n.308T>A n.476T>A | |
1 | g.155235753C>A | CA342713153 | GBA1 | c.1316G>T (p.Ser439Ile) c.1169G>T (p.Ser390Ile) c.1055G>T (p.Ser352Ile) n.83G>T n.307G>T n.475G>T | |
1 | g.155235753C= | CA2481201691 | GBA1 | c.1316G= (p.Ser439=) c.1169G= (p.Ser390=) c.1055G= (p.Ser352=) n.83G= n.307G= n.475G= | |
1 | g.155235753C>G | CA342713174 | GBA1 | c.1316G>C (p.Ser439Thr) c.1169G>C (p.Ser390Thr) c.1055G>C (p.Ser352Thr) n.83G>C n.307G>C n.475G>C | |
1 | g.155235753C>T | CA342713181 | GBA1 | c.1316G>A (p.Ser439Asn) c.1169G>A (p.Ser390Asn) c.1055G>A (p.Ser352Asn) n.83G>A n.307G>A n.475G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
1 | g.155235754T>A | CA342713185 | GBA1 | c.1315A>T (p.Ser439Cys) c.1168A>T (p.Ser390Cys) c.1054A>T (p.Ser352Cys) n.82A>T n.306A>T n.474A>T | |
1 | g.155235754T>C | CA342713186 | GBA1 | c.1315A>G (p.Ser439Gly) c.1168A>G (p.Ser390Gly) c.1054A>G (p.Ser352Gly) n.82A>G n.306A>G n.474A>G | |
1 | g.155235754T>G | CA342713188 | GBA1 | c.1315A>C (p.Ser439Arg) c.1168A>C (p.Ser390Arg) c.1054A>C (p.Ser352Arg) n.82A>C n.306A>C n.474A>C | |
1 | g.155235755G>A | CA1141556 | GBA1 | c.1314C>T (p.Asp438=) c.1167C>T (p.Asp389=) c.1053C>T (p.Asp351=) n.81C>T n.305C>T n.473C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.155235755G>C | CA30894478 | GBA1 | c.1314C>G (p.Asp438Glu) c.1167C>G (p.Asp389Glu) c.1053C>G (p.Asp351Glu) n.81C>G n.305C>G n.473C>G | dbSNP |
1 | g.155235755G= | CA1140925642 | GBA1 | c.1314C= (p.Asp438=) c.1167C= (p.Asp389=) c.1053C= (p.Asp351=) n.81C= n.305C= n.473C= | |
1 | g.155235755G>T | CA342713200 | GBA1 | c.1314C>A (p.Asp438Glu) c.1167C>A (p.Asp389Glu) c.1053C>A (p.Asp351Glu) n.81C>A n.305C>A n.473C>A | |
1 | g.155235756T>A | CA342713212 | GBA1 | c.1313A>T (p.Asp438Val) c.1166A>T (p.Asp389Val) c.1052A>T (p.Asp351Val) n.80A>T n.304A>T n.472A>T | |
1 | g.155235756T>C | CA342713216 | GBA1 | c.1313A>G (p.Asp438Gly) c.1166A>G (p.Asp389Gly) c.1052A>G (p.Asp351Gly) n.80A>G n.304A>G n.472A>G | |
1 | g.155235756T>G | CA342713219 | GBA1 | c.1313A>C (p.Asp438Ala) c.1166A>C (p.Asp389Ala) c.1052A>C (p.Asp351Ala) n.80A>C n.304A>C n.472A>C | |
1 | g.155235757C>A | CA342713235 | GBA1 | c.1312G>T (p.Asp438Tyr) c.1165G>T (p.Asp389Tyr) c.1051G>T (p.Asp351Tyr) n.79G>T n.303G>T n.471G>T | ClinVar |
1 | g.155235757C= | CA2481201692 | GBA1 | c.1312G= (p.Asp438=) c.1165G= (p.Asp389=) c.1051G= (p.Asp351=) n.79G= n.303G= n.471G= | |
1 | g.155235757C>G | CA342713226 | GBA1 | c.1312G>C (p.Asp438His) c.1165G>C (p.Asp389His) c.1051G>C (p.Asp351His) n.79G>C n.303G>C n.471G>C | ClinVar dbSNP |
1 | g.155235757C>T | CA342713229 | GBA1 | c.1312G>A (p.Asp438Asn) c.1165G>A (p.Asp389Asn) c.1051G>A (p.Asp351Asn) n.79G>A n.303G>A n.471G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
1 | g.155235758G>A | CA1141557 | GBA1 | c.1311C>T (p.Val437=) c.1164C>T (p.Val388=) c.1050C>T (p.Val350=) n.78C>T n.302C>T n.470C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.155235758G>C | CA30894482 | GBA1 | c.1311C>G (p.Val437=) c.1164C>G (p.Val388=) c.1050C>G (p.Val350=) n.78C>G n.302C>G n.470C>G | dbSNP gnomAD v4 |
1 | g.155235758G= | CA1141122424 | GBA1 | c.1311C= (p.Val437=) c.1164C= (p.Val388=) c.1050C= (p.Val350=) n.78C= n.302C= n.470C= | |
1 | g.155235758G>T | CA30894485 | GBA1 | c.1311C>A (p.Val437=) c.1164C>A (p.Val388=) c.1050C>A (p.Val350=) n.78C>A n.302C>A n.470C>A | dbSNP |
1 | g.155235759A>C | CA342713247 | GBA1 | c.1310T>G (p.Val437Gly) c.1163T>G (p.Val388Gly) c.1049T>G (p.Val350Gly) n.77T>G n.301T>G n.469T>G | |
1 | g.155235759A>G | CA342713251 | GBA1 | c.1310T>C (p.Val437Ala) c.1163T>C (p.Val388Ala) c.1049T>C (p.Val350Ala) n.77T>C n.301T>C n.469T>C | |
1 | g.155235759A>T | CA342713253 | GBA1 | c.1310T>A (p.Val437Asp) c.1163T>A (p.Val388Asp) c.1049T>A (p.Val350Asp) n.77T>A n.301T>A n.469T>A | |
1 | g.155235760del | CA2586967441 | GBA1 | c.1309del (p.Val437SerfsTer7) c.1162del (p.Val388SerfsTer7) c.1048del (p.Val350SerfsTer7) n.76del n.300del n.468del | |
1 | g.155235760C>A | CA253069 | GBA1 | c.1309G>T (p.Val437Phe) c.1162G>T (p.Val388Phe) c.1048G>T (p.Val350Phe) n.76G>T n.300G>T n.468G>T | ClinVar dbSNP COSMIC |
1 | g.155235760C= | CA1141581077 | GBA1 | c.1309G= (p.Val437=) c.1162G= (p.Val388=) c.1048G= (p.Val350=) n.76G= n.300G= n.468G= | |
1 | g.155235760C>G | CA342713274 | GBA1 | c.1309G>C (p.Val437Leu) c.1162G>C (p.Val388Leu) c.1048G>C (p.Val350Leu) n.76G>C n.300G>C n.468G>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.155235760C>T | CA342713276 | GBA1 | c.1309G>A (p.Val437Ile) c.1162G>A (p.Val388Ile) c.1048G>A (p.Val350Ile) n.76G>A n.300G>A n.468G>A | |
1 | g.155235761A= | CA2481201693 | GBA1 | c.1308T= (p.Phe436=) c.1161T= (p.Phe387=) c.1047T= (p.Phe349=) n.75T= n.299T= n.467T= | |
1 | g.155235761A>C | CA342713280 | GBA1 | c.1308T>G (p.Phe436Leu) c.1161T>G (p.Phe387Leu) c.1047T>G (p.Phe349Leu) n.75T>G n.299T>G n.467T>G | |
1 | g.155235761A>G | CA421020317 | GBA1 | c.1308T>C (p.Phe436=) c.1161T>C (p.Phe387=) c.1047T>C (p.Phe349=) n.75T>C n.299T>C n.467T>C | |
1 | g.155235761A>T | CA342713300 | GBA1 | c.1308T>A (p.Phe436Leu) c.1161T>A (p.Phe387Leu) c.1047T>A (p.Phe349Leu) n.75T>A n.299T>A n.467T>A | dbSNP |
1 | g.155235762A= | CA1140933546 | GBA1 | c.1307T= (p.Phe436=) c.1160T= (p.Phe387=) c.1046T= (p.Phe349=) n.74T= n.298T= n.466T= | |
1 | g.155235762A>C | CA342713307 | GBA1 | c.1307T>G (p.Phe436Cys) c.1160T>G (p.Phe387Cys) c.1046T>G (p.Phe349Cys) n.74T>G n.298T>G n.466T>G | |
1 | g.155235762A>G | CA30894487 | GBA1 | c.1307T>C (p.Phe436Ser) c.1160T>C (p.Phe387Ser) c.1046T>C (p.Phe349Ser) n.74T>C n.298T>C n.466T>C | ClinVar dbSNP gnomAD v4 |
1 | g.155235762A>T | CA342713304 | GBA1 | c.1307T>A (p.Phe436Tyr) c.1160T>A (p.Phe387Tyr) c.1046T>A (p.Phe349Tyr) n.74T>A n.298T>A n.466T>A | |
1 | g.155235763A>C | CA342713323 | GBA1 | c.1306T>G (p.Phe436Val) c.1159T>G (p.Phe387Val) c.1045T>G (p.Phe349Val) n.73T>G n.297T>G n.465T>G | |
1 | g.155235763A>G | CA342713328 | GBA1 | c.1306T>C (p.Phe436Leu) c.1159T>C (p.Phe387Leu) c.1045T>C (p.Phe349Leu) n.73T>C n.297T>C n.465T>C | |
1 | g.155235763A>T | CA342713329 | GBA1 | c.1306T>A (p.Phe436Ile) c.1159T>A (p.Phe387Ile) c.1045T>A (p.Phe349Ile) n.73T>A n.297T>A n.465T>A | |
1 | g.155235764G>A | CA1141559 | GBA1 | c.1305C>T (p.Asn435=) c.1158C>T (p.Asn386=) c.1044C>T (p.Asn348=) n.72C>T n.296C>T n.464C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.155235764G>C | CA1141558 | GBA1 | c.1305C>G (p.Asn435Lys) c.1158C>G (p.Asn386Lys) c.1044C>G (p.Asn348Lys) n.72C>G n.296C>G n.464C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.155235764G= | CA2481201694 | GBA1 | c.1305C= (p.Asn435=) c.1158C= (p.Asn386=) c.1044C= (p.Asn348=) n.72C= n.296C= n.464C= | |
1 | g.155235764G>T | CA342713330 | GBA1 | c.1305C>A (p.Asn435Lys) c.1158C>A (p.Asn386Lys) c.1044C>A (p.Asn348Lys) n.72C>A n.296C>A n.464C>A | |
1 | g.155235765T>A | CA342713332 | GBA1 | c.1304A>T (p.Asn435Ile) c.1157A>T (p.Asn386Ile) c.1043A>T (p.Asn348Ile) n.71A>T n.295A>T n.463A>T | |
1 | g.155235765T>C | CA342713337 | GBA1 | c.1304A>G (p.Asn435Ser) c.1157A>G (p.Asn386Ser) c.1043A>G (p.Asn348Ser) n.71A>G n.295A>G n.463A>G | |
1 | g.155235765T>G | CA30894493 | GBA1 | c.1304A>C (p.Asn435Thr) c.1157A>C (p.Asn386Thr) c.1043A>C (p.Asn348Thr) n.71A>C n.295A>C n.463A>C | dbSNP |
1 | g.155235765T= | CA1140940955 | GBA1 | c.1304A= (p.Asn435=) c.1157A= (p.Asn386=) c.1043A= (p.Asn348=) n.71A= n.295A= n.463A= | |
1 | g.155235766T>A | CA342713343 | GBA1 | c.1303A>T (p.Asn435Tyr) c.1156A>T (p.Asn386Tyr) c.1042A>T (p.Asn348Tyr) n.70A>T n.294A>T n.462A>T | |
1 | g.155235766T>C | CA342713345 | GBA1 | c.1303A>G (p.Asn435Asp) c.1156A>G (p.Asn386Asp) c.1042A>G (p.Asn348Asp) n.70A>G n.294A>G n.462A>G | |
1 | g.155235766T>G | CA342713350 | GBA1 | c.1303A>C (p.Asn435His) c.1156A>C (p.Asn386His) c.1042A>C (p.Asn348His) n.70A>C n.294A>C n.462A>C | gnomAD v4 |
1 | g.155235767A= | CA2481201695 | GBA1 | c.1302T= (p.Arg434=) c.1155T= (p.Arg385=) c.1041T= (p.Arg347=) n.69T= n.293T= n.461T= | |
1 | g.155235767A>C | CA421020319 | GBA1 | c.1302T>G (p.Arg434=) c.1155T>G (p.Arg385=) c.1041T>G (p.Arg347=) n.69T>G n.293T>G n.461T>G | |
1 | g.155235767A>G | CA1141560 | GBA1 | c.1302T>C (p.Arg434=) c.1155T>C (p.Arg385=) c.1041T>C (p.Arg347=) n.69T>C n.293T>C n.461T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.155235767A>T | CA421020320 | GBA1 | c.1302T>A (p.Arg434=) c.1155T>A (p.Arg385=) c.1041T>A (p.Arg347=) n.69T>A n.293T>A n.461T>A | ClinVar dbSNP |
1 | g.155235768C>A | CA342713358 | GBA1 | c.1301G>T (p.Arg434Leu) c.1154G>T (p.Arg385Leu) c.1040G>T (p.Arg347Leu) n.68G>T n.292G>T n.460G>T | COSMIC |
1 | g.155235768C= | CA2481201696 | GBA1 | c.1301G= (p.Arg434=) c.1154G= (p.Arg385=) c.1040G= (p.Arg347=) n.68G= n.292G= n.460G= | |
1 | g.155235768C>G | CA342713357 | GBA1 | c.1301G>C (p.Arg434Pro) c.1154G>C (p.Arg385Pro) c.1040G>C (p.Arg347Pro) n.68G>C n.292G>C n.460G>C | dbSNP |
1 | g.155235768C>T | CA1141561 | GBA1 | c.1301G>A (p.Arg434His) c.1154G>A (p.Arg385His) c.1040G>A (p.Arg347His) n.68G>A n.292G>A n.460G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.155235769G>A | CA342713359 | GBA1 | c.1300C>T (p.Arg434Cys) c.1153C>T (p.Arg385Cys) c.1039C>T (p.Arg347Cys) n.67C>T n.291C>T n.459C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.155235769G>C | CA1141562 | GBA1 | c.1300C>G (p.Arg434Gly) c.1153C>G (p.Arg385Gly) c.1039C>G (p.Arg347Gly) n.67C>G n.291C>G n.459C>G | dbSNP ExAC gnomAD v2 |
1 | g.155235769G= | CA1148450077 | GBA1 | c.1300C= (p.Arg434=) c.1153C= (p.Arg385=) c.1039C= (p.Arg347=) n.67C= n.291C= n.459C= | |
1 | g.155235769G>T | CA342713367 | GBA1 | c.1300C>A (p.Arg434Ser) c.1153C>A (p.Arg385Ser) c.1039C>A (p.Arg347Ser) n.67C>A n.291C>A n.459C>A | gnomAD v4 |
1 | g.155235770C>A | CA421020326 | GBA1 | c.1299G>T (p.Val433=) c.1152G>T (p.Val384=) c.1038G>T (p.Val346=) n.66G>T n.290G>T n.458G>T | |
1 | g.155235770C>G | CA421020324 | GBA1 | c.1299G>C (p.Val433=) c.1152G>C (p.Val384=) c.1038G>C (p.Val346=) n.66G>C n.290G>C n.458G>C | |
1 | g.155235770C>T | CA421020325 | GBA1 | c.1299G>A (p.Val433=) c.1152G>A (p.Val384=) c.1038G>A (p.Val346=) n.66G>A n.290G>A n.458G>A | gnomAD v4 |
1 | g.155235771A>C | CA342713373 | GBA1 | c.1298T>G (p.Val433Gly) c.1151T>G (p.Val384Gly) c.1037T>G (p.Val346Gly) n.65T>G n.289T>G n.457T>G | |
1 | g.155235771A>G | CA342713377 | GBA1 | c.1298T>C (p.Val433Ala) c.1151T>C (p.Val384Ala) c.1037T>C (p.Val346Ala) n.65T>C n.289T>C n.457T>C | gnomAD v4 |
1 | g.155235771A>T | CA342713379 | GBA1 | c.1298T>A (p.Val433Glu) c.1151T>A (p.Val384Glu) c.1037T>A (p.Val346Glu) n.65T>A n.289T>A n.457T>A | |
1 | g.155235772C>A | CA253059 | GBA1 | c.1297G>T (p.Val433Leu) c.1150G>T (p.Val384Leu) c.1036G>T (p.Val346Leu) n.64G>T n.288G>T n.456G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.155235772C= | CA1141188038 | GBA1 | c.1297G= (p.Val433=) c.1150G= (p.Val384=) c.1036G= (p.Val346=) n.64G= n.288G= n.456G= | |
1 | g.155235772C>G | CA342713384 | GBA1 | c.1297G>C (p.Val433Leu) c.1150G>C (p.Val384Leu) c.1036G>C (p.Val346Leu) n.64G>C n.288G>C n.456G>C | |
1 | g.155235772C>T | CA342713395 | GBA1 | c.1297G>A (p.Val433Met) c.1150G>A (p.Val384Met) c.1036G>A (p.Val346Met) n.64G>A n.288G>A n.456G>A | |
1 | g.155235773C>A | CA342713409 | GBA1 | c.1296G>T (p.Trp432Cys) c.1149G>T (p.Trp383Cys) c.1035G>T (p.Trp345Cys) n.63G>T n.287G>T n.455G>T | |
1 | g.155235773C= | CA2481201697 | GBA1 | c.1296G= (p.Trp432=) c.1149G= (p.Trp383=) c.1035G= (p.Trp345=) n.63G= n.287G= n.455G= | |
1 | g.155235773C>G | CA342713413 | GBA1 | c.1296G>C (p.Trp432Cys) c.1149G>C (p.Trp383Cys) c.1035G>C (p.Trp345Cys) n.63G>C n.287G>C n.455G>C | |
1 | g.155235773C>T | CA342713418 | GBA1 | c.1296G>A (p.Trp432Ter) c.1149G>A (p.Trp383Ter) c.1035G>A (p.Trp345Ter) n.63G>A n.287G>A n.455G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.155235774C>A | CA342713433 | GBA1 | c.1295G>T (p.Trp432Leu) c.1148G>T (p.Trp383Leu) c.1034G>T (p.Trp345Leu) n.62G>T n.286G>T n.454G>T | |
1 | g.155235774C>G | CA342713458 | GBA1 | c.1295G>C (p.Trp432Ser) c.1148G>C (p.Trp383Ser) c.1034G>C (p.Trp345Ser) n.62G>C n.286G>C n.454G>C | gnomAD v4 |
1 | g.155235774C>T | CA342713453 | GBA1 | c.1295G>A (p.Trp432Ter) c.1148G>A (p.Trp383Ter) c.1034G>A (p.Trp345Ter) n.62G>A n.286G>A n.454G>A | |
1 | g.155235775A= | CA2481201698 | GBA1 | c.1294T= (p.Trp432=) c.1147T= (p.Trp383=) c.1033T= (p.Trp345=) n.61T= n.285T= n.453T= | |
1 | g.155235775A>C | CA342713462 | GBA1 | c.1294T>G (p.Trp432Gly) c.1147T>G (p.Trp383Gly) c.1033T>G (p.Trp345Gly) n.61T>G n.285T>G n.453T>G | |
1 | g.155235775A>G | CA342713484 | GBA1 | c.1294T>C (p.Trp432Arg) c.1147T>C (p.Trp383Arg) c.1033T>C (p.Trp345Arg) n.61T>C n.285T>C n.453T>C | |
1 | g.155235775A>T | CA342713466 | GBA1 | c.1294T>A (p.Trp432Arg) c.1147T>A (p.Trp383Arg) c.1033T>A (p.Trp345Arg) n.61T>A n.285T>A n.453T>A | ClinVar dbSNP gnomAD v4 |
1 | g.155235776A= | CA2481201699 | GBA1 | c.1293T= (p.Asn431=) c.1146T= (p.Asn382=) c.1032T= (p.Asn344=) n.60T= n.284T= n.452T= | |
1 | g.155235776A>C | CA342713489 | GBA1 | c.1293T>G (p.Asn431Lys) c.1146T>G (p.Asn382Lys) c.1032T>G (p.Asn344Lys) n.60T>G n.284T>G n.452T>G | |
1 | g.155235776A>G | CA1141563 | GBA1 | c.1293T>C (p.Asn431=) c.1146T>C (p.Asn382=) c.1032T>C (p.Asn344=) n.60T>C n.284T>C n.452T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.155235776A>T | CA342713492 | GBA1 | c.1293T>A (p.Asn431Lys) c.1146T>A (p.Asn382Lys) c.1032T>A (p.Asn344Lys) n.60T>A n.284T>A n.452T>A | |
1 | g.155235777T>A | CA30894498 | GBA1 | c.1292A>T (p.Asn431Ile) c.1145A>T (p.Asn382Ile) c.1031A>T (p.Asn344Ile) n.59A>T n.283A>T n.451A>T | dbSNP |
1 | g.155235777T>C | CA1141564 | GBA1 | c.1292A>G (p.Asn431Ser) c.1145A>G (p.Asn382Ser) c.1031A>G (p.Asn344Ser) n.59A>G n.283A>G n.451A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.155235777T>G | CA342713512 | GBA1 | c.1292A>C (p.Asn431Thr) c.1145A>C (p.Asn382Thr) c.1031A>C (p.Asn344Thr) n.59A>C n.283A>C n.451A>C | dbSNP |
1 | g.155235777T= | CA1141057797 | GBA1 | c.1292A= (p.Asn431=) c.1145A= (p.Asn382=) c.1031A= (p.Asn344=) n.59A= n.283A= n.451A= | |
1 | g.155235778T>A | CA342713514 | GBA1 | c.1291A>T (p.Asn431Tyr) c.1144A>T (p.Asn382Tyr) c.1030A>T (p.Asn344Tyr) n.58A>T n.282A>T n.450A>T | |
1 | g.155235778T>C | CA342713515 | GBA1 | c.1291A>G (p.Asn431Asp) c.1144A>G (p.Asn382Asp) c.1030A>G (p.Asn344Asp) n.58A>G n.282A>G n.450A>G | |
1 | g.155235778T>G | CA342713516 | GBA1 | c.1291A>C (p.Asn431His) c.1144A>C (p.Asn382His) c.1030A>C (p.Asn344His) n.58A>C n.282A>C n.450A>C | |
1 | g.155235779G>A | CA421020330 | GBA1 | c.1290C>T (p.Pro430=) c.1143C>T (p.Pro381=) c.1029C>T (p.Pro343=) n.57C>T n.281C>T n.449C>T | ClinVar dbSNP gnomAD v4 |
1 | g.155235779G>C | CA421020331 | GBA1 | c.1290C>G (p.Pro430=) c.1143C>G (p.Pro381=) c.1029C>G (p.Pro343=) n.57C>G n.281C>G n.449C>G | |
1 | g.155235779G= | CA2481201700 | GBA1 | c.1290C= (p.Pro430=) c.1143C= (p.Pro381=) c.1029C= (p.Pro343=) n.57C= n.281C= n.449C= | |
1 | g.155235779G>T | CA421020332 | GBA1 | c.1290C>A (p.Pro430=) c.1143C>A (p.Pro381=) c.1029C>A (p.Pro343=) n.57C>A n.281C>A n.449C>A | |
1 | g.155235780G>A | CA30894500 | GBA1 | c.1289C>T (p.Pro430Leu) c.1142C>T (p.Pro381Leu) c.1028C>T (p.Pro343Leu) n.56C>T n.280C>T n.448C>T | ClinVar dbSNP gnomAD v4 |
1 | g.155235780G>C | CA342713521 | GBA1 | c.1289C>G (p.Pro430Arg) c.1142C>G (p.Pro381Arg) c.1028C>G (p.Pro343Arg) n.56C>G n.280C>G n.448C>G | |
1 | g.155235780G= | CA1141017487 | GBA1 | c.1289C= (p.Pro430=) c.1142C= (p.Pro381=) c.1028C= (p.Pro343=) n.56C= n.280C= n.448C= | |
1 | g.155235780G>T | CA342713523 | GBA1 | c.1289C>A (p.Pro430His) c.1142C>A (p.Pro381His) c.1028C>A (p.Pro343His) n.56C>A n.280C>A n.448C>A | |
1 | g.155235781G>A | CA342713525 | GBA1 | c.1288C>T (p.Pro430Ser) c.1141C>T (p.Pro381Ser) c.1027C>T (p.Pro343Ser) n.55C>T n.279C>T n.447C>T | |
1 | g.155235781G>C | CA342713527 | GBA1 | c.1288C>G (p.Pro430Ala) c.1141C>G (p.Pro381Ala) c.1027C>G (p.Pro343Ala) n.55C>G n.279C>G n.447C>G | gnomAD v4 |
1 | g.155235781G>T | CA342713529 | GBA1 | c.1288C>A (p.Pro430Thr) c.1141C>A (p.Pro381Thr) c.1027C>A (p.Pro343Thr) n.55C>A n.279C>A n.447C>A | |
1 | g.155235782T>A | CA421020335 | GBA1 | c.1287A>T (p.Gly429=) c.1140A>T (p.Gly380=) c.1026A>T (p.Gly342=) n.54A>T n.278A>T n.446A>T | gnomAD v4 |
1 | g.155235782T>C | CA421020337 | GBA1 | c.1287A>G (p.Gly429=) c.1140A>G (p.Gly380=) c.1026A>G (p.Gly342=) n.54A>G n.278A>G n.446A>G | |
1 | g.155235782T>G | CA421020339 | GBA1 | c.1287A>C (p.Gly429=) c.1140A>C (p.Gly380=) c.1026A>C (p.Gly342=) n.54A>C n.278A>C n.446A>C | |
1 | g.155235783C>A | CA342713544 | GBA1 | c.1286G>T (p.Gly429Val) c.1139G>T (p.Gly380Val) c.1025G>T (p.Gly342Val) n.53G>T n.277G>T n.445G>T | |
1 | g.155235783C>G | CA342713535 | GBA1 | c.1286G>C (p.Gly429Ala) c.1139G>C (p.Gly380Ala) c.1025G>C (p.Gly342Ala) n.53G>C n.277G>C n.445G>C | |
1 | g.155235783C>T | CA342713536 | GBA1 | c.1286G>A (p.Gly429Glu) c.1139G>A (p.Gly380Glu) c.1025G>A (p.Gly342Glu) n.53G>A n.277G>A n.445G>A | |
1 | g.155235784C>A | CA342713545 | GBA1 | c.1285G>T (p.Gly429Ter) c.1138G>T (p.Gly380Ter) c.1024G>T (p.Gly342Ter) n.52G>T n.276G>T n.444G>T | |
1 | g.155235784C>G | CA342713550 | GBA1 | c.1285G>C (p.Gly429Arg) c.1138G>C (p.Gly380Arg) c.1024G>C (p.Gly342Arg) n.52G>C n.276G>C n.444G>C | |
1 | g.155235784C>T | CA342713553 | GBA1 | c.1285G>A (p.Gly429Arg) c.1138G>A (p.Gly380Arg) c.1024G>A (p.Gly342Arg) n.52G>A n.276G>A n.444G>A | |
1 | g.155235785T>A | CA421020343 | GBA1 | c.1284A>T (p.Gly428=) c.1137A>T (p.Gly379=) c.1023A>T (p.Gly341=) n.51A>T n.275A>T n.443A>T | |
1 | g.155235785T>C | CA421020344 | GBA1 | c.1284A>G (p.Gly428=) c.1137A>G (p.Gly379=) c.1023A>G (p.Gly341=) n.51A>G n.275A>G n.443A>G | gnomAD v4 |
1 | g.155235785T>G | CA421020345 | GBA1 | c.1284A>C (p.Gly428=) c.1137A>C (p.Gly379=) c.1023A>C (p.Gly341=) n.51A>C n.275A>C n.443A>C | ClinVar dbSNP |
1 | g.155235786C>A | CA342713554 | GBA1 | c.1283G>T (p.Gly428Val) c.1136G>T (p.Gly379Val) c.1022G>T (p.Gly341Val) n.50G>T n.274G>T n.442G>T | |
1 | g.155235786C>G | CA342713555 | GBA1 | c.1283G>C (p.Gly428Ala) c.1136G>C (p.Gly379Ala) c.1022G>C (p.Gly341Ala) n.50G>C n.274G>C n.442G>C | |
1 | g.155235786C>T | CA342713556 | GBA1 | c.1283G>A (p.Gly428Glu) c.1136G>A (p.Gly379Glu) c.1022G>A (p.Gly341Glu) n.50G>A n.274G>A n.442G>A | |
1 | g.155235787C>A | CA342713557 | GBA1 | c.1282G>T (p.Gly428Ter) c.1135G>T (p.Gly379Ter) c.1021G>T (p.Gly341Ter) n.49G>T n.273G>T n.441G>T | gnomAD v4 |
1 | g.155235787C>G | CA342713559 | GBA1 | c.1282G>C (p.Gly428Arg) c.1135G>C (p.Gly379Arg) c.1021G>C (p.Gly341Arg) n.49G>C n.273G>C n.441G>C | |
1 | g.155235787C>T | CA342713563 | GBA1 | c.1282G>A (p.Gly428Arg) c.1135G>A (p.Gly379Arg) c.1021G>A (p.Gly341Arg) n.49G>A n.273G>A n.441G>A | gnomAD v4 |
1 | g.155235788_155235790del | CA2586967442 | GBA1 | c.1280_1282del (p.Glu427del) c.1133_1135del (p.Glu378del) c.1019_1021del (p.Glu340del) n.47_49del n.271_273del n.439_441del | |
1 | g.155235788T>A | CA342713567 | GBA1 | c.1281A>T (p.Glu427Asp) c.1134A>T (p.Glu378Asp) c.1020A>T (p.Glu340Asp) n.48A>T n.272A>T n.440A>T | |
1 | g.155235788T>C | CA421020349 | GBA1 | c.1281A>G (p.Glu427=) c.1134A>G (p.Glu378=) c.1020A>G (p.Glu340=) n.48A>G n.272A>G n.440A>G | ClinVar dbSNP |
1 | g.155235788T>G | CA342713568 | GBA1 | c.1281A>C (p.Glu427Asp) c.1134A>C (p.Glu378Asp) c.1020A>C (p.Glu340Asp) n.48A>C n.272A>C n.440A>C | |
1 | g.155235788T= | CA2481201701 | GBA1 | c.1281A= (p.Glu427=) c.1134A= (p.Glu378=) c.1020A= (p.Glu340=) n.48A= n.272A= n.440A= | |
1 | g.155235789T>A | CA342713572 | GBA1 | c.1280A>T (p.Glu427Val) c.1133A>T (p.Glu378Val) c.1019A>T (p.Glu340Val) n.47A>T n.271A>T n.439A>T | gnomAD v4 |
1 | g.155235789T>C | CA342713570 | GBA1 | c.1280A>G (p.Glu427Gly) c.1133A>G (p.Glu378Gly) c.1019A>G (p.Glu340Gly) n.47A>G n.271A>G n.439A>G | |
1 | g.155235789T>G | CA342713569 | GBA1 | c.1280A>C (p.Glu427Ala) c.1133A>C (p.Glu378Ala) c.1019A>C (p.Glu340Ala) n.47A>C n.271A>C n.439A>C | |
1 | g.155235789_155235790delinsCGGGGTTCAGGG | CA2586967443 | GBA1 | c.1279_1280delinsCCCTGAACCCCG (p.Glu427ProfsTer2) c.1132_1133delinsCCCTGAACCCCG (p.Glu378ProfsTer2) c.1018_1019delinsCCCTGAACCCCG (p.Glu340ProfsTer2) n.46_47delinsCCCTGAACCCCG n.270_271delinsCCCTGAACCCCG n.438_439delinsCCCTGAACCCCG | |
1 | g.155235790C>A | CA342713575 | GBA1 | c.1279G>T (p.Glu427Ter) c.1132G>T (p.Glu378Ter) c.1018G>T (p.Glu340Ter) n.46G>T n.270G>T n.438G>T | ClinVar dbSNP |
1 | g.155235790C= | CA1142286131 | GBA1 | c.1279G= (p.Glu427=) c.1132G= (p.Glu378=) c.1018G= (p.Glu340=) n.46G= n.270G= n.438G= | |
1 | g.155235790C>G | CA342713573 | GBA1 | c.1279G>C (p.Glu427Gln) c.1132G>C (p.Glu378Gln) c.1018G>C (p.Glu340Gln) n.46G>C n.270G>C n.438G>C | |
1 | g.155235790C>T | CA1141565 | GBA1 | c.1279G>A (p.Glu427Lys) c.1132G>A (p.Glu378Lys) c.1018G>A (p.Glu340Lys) n.46G>A n.270G>A n.438G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.155235791G>A | CA30894509 | GBA1 | c.1278C>T (p.Pro426=) c.1131C>T (p.Pro377=) c.1017C>T (p.Pro339=) n.45C>T n.269C>T n.437C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.155235791G>C | CA421020354 | GBA1 | c.1278C>G (p.Pro426=) c.1131C>G (p.Pro377=) c.1017C>G (p.Pro339=) n.45C>G n.269C>G n.437C>G | dbSNP gnomAD v3 gnomAD v4 |
1 | g.155235791G= | CA1143487031 | GBA1 | c.1278C= (p.Pro426=) c.1131C= (p.Pro377=) c.1017C= (p.Pro339=) n.45C= n.269C= n.437C= | |
1 | g.155235791G>T | CA421020353 | GBA1 | c.1278C>A (p.Pro426=) c.1131C>A (p.Pro377=) c.1017C>A (p.Pro339=) n.45C>A n.269C>A n.437C>A | |
1 | g.155235792G>A | CA16044122 | GBA1 | c.1277C>T (p.Pro426Leu) c.1130C>T (p.Pro377Leu) c.1016C>T (p.Pro339Leu) n.44C>T n.268C>T n.436C>T | ClinVar dbSNP gnomAD v4 COSMIC |
1 | g.155235792G>C | CA342713593 | GBA1 | c.1277C>G (p.Pro426Arg) c.1130C>G (p.Pro377Arg) c.1016C>G (p.Pro339Arg) n.44C>G n.268C>G n.436C>G | gnomAD v4 |
1 | g.155235792G= | CA2481201702 | GBA1 | c.1277C= (p.Pro426=) c.1130C= (p.Pro377=) c.1016C= (p.Pro339=) n.44C= n.268C= n.436C= | |
1 | g.155235792G>T | CA342713594 | GBA1 | c.1277C>A (p.Pro426His) c.1130C>A (p.Pro377His) c.1016C>A (p.Pro339His) n.44C>A n.268C>A n.436C>A | |
1 | g.155235793G>A | CA342713614 | GBA1 | c.1276C>T (p.Pro426Ser) c.1129C>T (p.Pro377Ser) c.1015C>T (p.Pro339Ser) n.43C>T n.267C>T n.435C>T | gnomAD v4 |
1 | g.155235793G>C | CA342713599 | GBA1 | c.1276C>G (p.Pro426Ala) c.1129C>G (p.Pro377Ala) c.1015C>G (p.Pro339Ala) n.43C>G n.267C>G n.435C>G | |
1 | g.155235793G>T | CA342713602 | GBA1 | c.1276C>A (p.Pro426Thr) c.1129C>A (p.Pro377Thr) c.1015C>A (p.Pro339Thr) n.43C>A n.267C>A n.435C>A | |
1 | g.155235794G>A | CA421020358 | GBA1 | c.1275C>T (p.Asn425=) c.1128C>T (p.Asn376=) c.1014C>T (p.Asn338=) n.42C>T n.266C>T n.434C>T | dbSNP gnomAD v4 |
1 | g.155235794G>C | CA342713626 | GBA1 | c.1275C>G (p.Asn425Lys) c.1128C>G (p.Asn376Lys) c.1014C>G (p.Asn338Lys) n.42C>G n.266C>G n.434C>G | |
1 | g.155235794G= | CA2481201703 | GBA1 | c.1275C= (p.Asn425=) c.1128C= (p.Asn376=) c.1014C= (p.Asn338=) n.42C= n.266C= n.434C= | |
1 | g.155235794G>T | CA30894515 | GBA1 | c.1275C>A (p.Asn425Lys) c.1128C>A (p.Asn376Lys) c.1014C>A (p.Asn338Lys) n.42C>A n.266C>A n.434C>A | ClinVar dbSNP gnomAD v4 |
1 | g.155235795T>A | CA342713637 | GBA1 | c.1274A>T (p.Asn425Ile) c.1127A>T (p.Asn376Ile) c.1013A>T (p.Asn338Ile) n.41A>T n.265A>T n.433A>T | |
1 | g.155235795T>C | CA342713638 | GBA1 | c.1274A>G (p.Asn425Ser) c.1127A>G (p.Asn376Ser) c.1013A>G (p.Asn338Ser) n.41A>G n.265A>G n.433A>G | |
1 | g.155235795T>G | CA342713639 | GBA1 | c.1274A>C (p.Asn425Thr) c.1127A>C (p.Asn376Thr) c.1013A>C (p.Asn338Thr) n.41A>C n.265A>C n.433A>C | |
1 | g.155235796dup | CA421020360 | GBA1 | c.1274dup (p.Asn425LysfsTer11) c.1127dup (p.Asn376LysfsTer11) c.1013dup (p.Asn338LysfsTer11) n.41dup n.265dup n.433dup | |
1 | g.155235796T>A | CA342713640 | GBA1 | c.1273A>T (p.Asn425Tyr) c.1126A>T (p.Asn376Tyr) c.1012A>T (p.Asn338Tyr) n.40A>T n.264A>T n.432A>T | |
1 | g.155235796T>C | CA342713642 | GBA1 | c.1273A>G (p.Asn425Asp) c.1126A>G (p.Asn376Asp) c.1012A>G (p.Asn338Asp) n.40A>G n.264A>G n.432A>G | |
1 | g.155235796T>G | CA342713641 | GBA1 | c.1273A>C (p.Asn425His) c.1126A>C (p.Asn376His) c.1012A>C (p.Asn338His) n.40A>C n.264A>C n.432A>C | |
1 | g.155235797C>A | CA421020361 | GBA1 | c.1272G>T (p.Leu424=) c.1125G>T (p.Leu375=) c.1011G>T (p.Leu337=) n.39G>T n.263G>T n.431G>T | |
1 | g.155235797C>G | CA421020362 | GBA1 | c.1272G>C (p.Leu424=) c.1125G>C (p.Leu375=) c.1011G>C (p.Leu337=) n.39G>C n.263G>C n.431G>C | ClinVar dbSNP |
1 | g.155235797C>T | CA421020363 | GBA1 | c.1272G>A (p.Leu424=) c.1125G>A (p.Leu375=) c.1011G>A (p.Leu337=) n.39G>A n.263G>A n.431G>A | |
1 | g.155235798A= | CA2481201704 | GBA1 | c.1271T= (p.Leu424=) c.1124T= (p.Leu375=) c.1010T= (p.Leu337=) n.38T= n.262T= n.430T= | |
1 | g.155235798A>C | CA342713643 | GBA1 | c.1271T>G (p.Leu424Arg) c.1124T>G (p.Leu375Arg) c.1010T>G (p.Leu337Arg) n.38T>G n.262T>G n.430T>G | |
1 | g.155235798A>G | CA1141566 | GBA1 | c.1271T>C (p.Leu424Pro) c.1124T>C (p.Leu375Pro) c.1010T>C (p.Leu337Pro) n.38T>C n.262T>C n.430T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.155235798A>T | CA342713651 | GBA1 | c.1271T>A (p.Leu424Gln) c.1124T>A (p.Leu375Gln) c.1010T>A (p.Leu337Gln) n.38T>A n.262T>A n.430T>A | |
1 | g.155235799G>A | CA421020364 | GBA1 | c.1270C>T (p.Leu424=) c.1123C>T (p.Leu375=) c.1009C>T (p.Leu337=) n.37C>T n.261C>T n.429C>T | ClinVar gnomAD v4 |
1 | g.155235799G>C | CA342713658 | GBA1 | c.1270C>G (p.Leu424Val) c.1123C>G (p.Leu375Val) c.1009C>G (p.Leu337Val) n.37C>G n.261C>G n.429C>G | |
1 | g.155235799G>T | CA342713663 | GBA1 | c.1270C>A (p.Leu424Met) c.1123C>A (p.Leu375Met) c.1009C>A (p.Leu337Met) n.37C>A n.261C>A n.429C>A | |
1 | g.155235800G>A | CA421020365 | GBA1 | c.1269C>T (p.Ala423=) c.1122C>T (p.Ala374=) c.1008C>T (p.Ala336=) n.36C>T n.260C>T n.428C>T | |
1 | g.155235800G>C | CA421020366 | GBA1 | c.1269C>G (p.Ala423=) c.1122C>G (p.Ala374=) c.1008C>G (p.Ala336=) n.36C>G n.260C>G n.428C>G | |
1 | g.155235800G>T | CA421020367 | GBA1 | c.1269C>A (p.Ala423=) c.1122C>A (p.Ala374=) c.1008C>A (p.Ala336=) n.36C>A n.260C>A n.428C>A | |
1 | g.155235801G>A | CA1141567 | GBA1 | c.1268C>T (p.Ala423Val) c.1121C>T (p.Ala374Val) c.1007C>T (p.Ala336Val) n.35C>T n.259C>T n.427C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.155235801G>C | CA342713666 | GBA1 | c.1268C>G (p.Ala423Gly) c.1121C>G (p.Ala374Gly) c.1007C>G (p.Ala336Gly) n.35C>G n.259C>G n.427C>G | |
1 | g.155235801G= | CA2481201705 | GBA1 | c.1268C= (p.Ala423=) c.1121C= (p.Ala374=) c.1007C= (p.Ala336=) n.35C= n.259C= n.427C= | |
1 | g.155235801G>T | CA342713667 | GBA1 | c.1268C>A (p.Ala423Asp) c.1121C>A (p.Ala374Asp) c.1007C>A (p.Ala336Asp) n.35C>A n.259C>A n.427C>A | |
1 | g.155235802C>A | CA342713671 | GBA1 | c.1267G>T (p.Ala423Ser) c.1120G>T (p.Ala374Ser) c.1006G>T (p.Ala336Ser) n.34G>T n.258G>T n.426G>T | COSMIC |
1 | g.155235802C>G | CA342713676 | GBA1 | c.1267G>C (p.Ala423Pro) c.1120G>C (p.Ala374Pro) c.1006G>C (p.Ala336Pro) n.34G>C n.258G>C n.426G>C | |
1 | g.155235802C>T | CA342713678 | GBA1 | c.1267G>A (p.Ala423Thr) c.1120G>A (p.Ala374Thr) c.1006G>A (p.Ala336Thr) n.34G>A n.258G>A n.426G>A | |
1 | g.155235803A= | CA2481201706 | GBA1 | c.1266T= (p.Leu422=) c.1119T= (p.Leu373=) c.1005T= (p.Leu335=) n.33T= n.257T= n.425T= | |
1 | g.155235803A>C | CA421020371 | GBA1 | c.1266T>G (p.Leu422=) c.1119T>G (p.Leu373=) c.1005T>G (p.Leu335=) n.33T>G n.257T>G n.425T>G | |
1 | g.155235803A>G | CA421020373 | GBA1 | c.1266T>C (p.Leu422=) c.1119T>C (p.Leu373=) c.1005T>C (p.Leu335=) n.33T>C n.257T>C n.425T>C | dbSNP |
1 | g.155235803A>T | CA421020372 | GBA1 | c.1266T>A (p.Leu422=) c.1119T>A (p.Leu373=) c.1005T>A (p.Leu335=) n.33T>A n.257T>A n.425T>A | dbSNP |
1 | g.155235804A= | CA2481201707 | GBA1 | c.1265T= (p.Leu422=) c.1118T= (p.Leu373=) c.1004T= (p.Leu335=) n.32T= n.256T= n.424T= | |
1 | g.155235804A>C | CA342713681 | GBA1 | c.1265T>G (p.Leu422Arg) c.1118T>G (p.Leu373Arg) c.1004T>G (p.Leu335Arg) n.32T>G n.256T>G n.424T>G | |
1 | g.155235804A>G | CA342713685 | GBA1 | c.1265T>C (p.Leu422Pro) c.1118T>C (p.Leu373Pro) c.1004T>C (p.Leu335Pro) n.32T>C n.256T>C n.424T>C | dbSNP gnomAD v2 |
1 | g.155235804A>T | CA342713680 | GBA1 | c.1265T>A (p.Leu422His) c.1118T>A (p.Leu373His) c.1004T>A (p.Leu335His) n.32T>A n.256T>A n.424T>A | |
1 | g.155235805G>A | CA342713693 | GBA1 | c.1264C>T (p.Leu422Phe) c.1117C>T (p.Leu373Phe) c.1003C>T (p.Leu335Phe) n.31C>T n.255C>T n.423C>T | |
1 | g.155235805G>C | CA342713697 | GBA1 | c.1264C>G (p.Leu422Val) c.1117C>G (p.Leu373Val) c.1003C>G (p.Leu335Val) n.31C>G n.255C>G n.423C>G | |
1 | g.155235805G= | CA1142899772 | GBA1 | c.1264C= (p.Leu422=) c.1117C= (p.Leu373=) c.1003C= (p.Leu335=) n.31C= n.255C= n.423C= | |
1 | g.155235805G>T | CA1141568 | GBA1 | c.1264C>A (p.Leu422Ile) c.1117C>A (p.Leu373Ile) c.1003C>A (p.Leu335Ile) n.31C>A n.255C>A n.423C>A | dbSNP ExAC gnomAD v3 gnomAD v4 |
1 | g.155235806G>A | CA421020377 | GBA1 | c.1263C>T (p.Asn421=) c.1116C>T (p.Asn372=) c.1002C>T (p.Asn334=) n.30C>T n.254C>T n.422C>T | |
1 | g.155235806G>C | CA342713700 | GBA1 | c.1263C>G (p.Asn421Lys) c.1116C>G (p.Asn372Lys) c.1002C>G (p.Asn334Lys) n.30C>G n.254C>G n.422C>G | |
1 | g.155235806G>T | CA342713714 | GBA1 | c.1263C>A (p.Asn421Lys) c.1116C>A (p.Asn372Lys) c.1002C>A (p.Asn334Lys) n.30C>A n.254C>A n.422C>A | ClinVar dbSNP |
1 | g.155235807T>A | CA342713725 | GBA1 | c.1262A>T (p.Asn421Ile) c.1115A>T (p.Asn372Ile) c.1001A>T (p.Asn334Ile) n.29A>T n.253A>T n.421A>T | COSMIC |
1 | g.155235807T>C | CA342713737 | GBA1 | c.1262A>G (p.Asn421Ser) c.1115A>G (p.Asn372Ser) c.1001A>G (p.Asn334Ser) n.29A>G n.253A>G n.421A>G | |
1 | g.155235807T>G | CA342713745 | GBA1 | c.1262A>C (p.Asn421Thr) c.1115A>C (p.Asn372Thr) c.1001A>C (p.Asn334Thr) n.29A>C n.253A>C n.421A>C | |
1 | g.155235808T>A | CA342713769 | GBA1 | c.1261A>T (p.Asn421Tyr) c.1114A>T (p.Asn372Tyr) c.1000A>T (p.Asn334Tyr) n.28A>T n.252A>T n.420A>T | |
1 | g.155235808T>C | CA342713786 | GBA1 | c.1261A>G (p.Asn421Asp) c.1114A>G (p.Asn372Asp) c.1000A>G (p.Asn334Asp) n.28A>G n.252A>G n.420A>G | |
1 | g.155235808T>G | CA342713802 | GBA1 | c.1261A>C (p.Asn421His) c.1114A>C (p.Asn372His) c.1000A>C (p.Asn334His) n.28A>C n.252A>C n.420A>C | ClinVar gnomAD v4 |