Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.32133666_32137711dupCA10575837SPASTc.*906-2897_*1153+523dup
c.1246-2897_1493+523dup
c.1243-2897_1490+523dup
c.983-2897_1230+523dup
c.1147-2897_1394+523dup
c.1020-2897_1267+523dup
c.988-2897_1235+523dup
c.405-2897_560+523dup
c.826-2897_1073+523dup
c.1122-2897_1369+523dup
c.892-2897_1139+523dup
n.1983-2897_2230+523dup
c.696-2897_943+523dup
c.593-3443_672+523dup
c.1150-2897_1397+523dup
n.938-2897_1185+523dup
c.746-2897_993+523dup
ClinVar
2g.32133667_32137711dupCA10575495SPASTc.*906-2896_*1153+523dup
c.1246-2896_1493+523dup
c.1243-2896_1490+523dup
c.983-2896_1230+523dup
c.1147-2896_1394+523dup
c.1020-2896_1267+523dup
c.988-2896_1235+523dup
c.405-2896_560+523dup
c.826-2896_1073+523dup
c.1122-2896_1369+523dup
c.892-2896_1139+523dup
n.1983-2896_2230+523dup
c.696-2896_943+523dup
c.593-3442_672+523dup
c.1150-2896_1397+523dup
n.938-2896_1185+523dup
c.746-2896_993+523dup
ClinVar
2g.32137136_32137141delCA2582342361SPASTc.*1101_*1106del (n.*1101_*1106del)
c.1441_1446del (p.Leu481_Val482del)
c.1438_1443del (p.Leu480_Val481del)
c.1178_1183del
c.1342_1347del (p.Leu448_Val449del)
c.1215_1220del
c.1183_1188del (p.Leu395_Val396del)
c.508_513del
c.1021_1026del
c.1317_1322del
c.1087_1092del (p.Leu363_Val364del)
n.2178_2183del
c.891_896del
c.620_625del
c.1087_1092del
c.1345_1350del (p.Leu449_Val450del)
n.1133_1138del
c.941_946del
ClinVar
2g.32137134_32137140delinsCCA2586964777SPASTc.*1099_*1105delinsC (n.*1099_*1105delinsC)
c.1439_1445delinsC (p.Val480_Val482delinsAla)
c.1436_1442delinsC (p.Val479_Val481delinsAla)
c.1176_1182delinsC
c.1340_1346delinsC (p.Val447_Val449delinsAla)
c.1213_1219delinsC
c.1181_1187delinsC (p.Val394_Val396delinsAla)
c.506_512delinsC
c.1019_1025delinsC
c.1315_1321delinsC
c.1085_1091delinsC (p.Val362_Val364delinsAla)
n.2176_2182delinsC
c.889_895delinsC
c.618_624delinsC
c.1085_1091delinsC
c.1343_1349delinsC (p.Val448_Val450delinsAla)
n.1131_1137delinsC
c.939_945delinsC
2g.32137137T>ACA346502438SPASTc.*1102T>A (n.*1102T>A)
c.1442T>A (p.Leu481His)
c.1439T>A (p.Leu480His)
c.1179T>A
c.1343T>A (p.Leu448His)
c.1216T>A
c.1184T>A (p.Leu395His)
c.509T>A
c.1022T>A
c.1318T>A
c.1088T>A (p.Leu363His)
n.2179T>A
c.892T>A
c.621T>A
c.1088T>A
c.1346T>A (p.Leu449His)
n.1134T>A
c.942T>A
2g.32137137T>CCA346502439SPASTc.*1102T>C (n.*1102T>C)
c.1442T>C (p.Leu481Pro)
c.1439T>C (p.Leu480Pro)
c.1179T>C
c.1343T>C (p.Leu448Pro)
c.1216T>C
c.1184T>C (p.Leu395Pro)
c.509T>C
c.1022T>C
c.1318T>C
c.1088T>C (p.Leu363Pro)
n.2179T>C
c.892T>C
c.621T>C
c.1088T>C
c.1346T>C (p.Leu449Pro)
n.1134T>C
c.942T>C
2g.32137137T>GCA346502440SPASTc.*1102T>G (n.*1102T>G)
c.1442T>G (p.Leu481Arg)
c.1439T>G (p.Leu480Arg)
c.1179T>G
c.1343T>G (p.Leu448Arg)
c.1216T>G
c.1184T>G (p.Leu395Arg)
c.509T>G
c.1022T>G
c.1318T>G
c.1088T>G (p.Leu363Arg)
n.2179T>G
c.892T>G
c.621T>G
c.1088T>G
c.1346T>G (p.Leu449Arg)
n.1134T>G
c.942T>G
2g.32137137T=CA1242502047SPASTc.*1102T= (n.*1102T=)
c.1442T= (p.Leu481=)
c.1439T= (p.Leu480=)
c.1179T=
c.1343T= (p.Leu448=)
c.1216T=
c.1184T= (p.Leu395=)
c.509T=
c.1022T=
c.1318T=
c.1088T= (p.Leu363=)
n.2179T=
c.892T=
c.621T=
c.1088T=
c.1346T= (p.Leu449=)
n.1134T=
c.942T=
2g.32137137_32137138insACA658657027SPASTc.*1102_*1103insA (n.*1102_*1103insA)
c.1442_1443insA (p.Val482CysfsTer6)
c.1439_1440insA (p.Val481CysfsTer6)
c.1179_1180insA
c.1343_1344insA (p.Val449CysfsTer6)
c.1216_1217insA
c.1184_1185insA (p.Val396CysfsTer6)
c.509_510insA
c.1022_1023insA
c.1318_1319insA
c.1088_1089insA (p.Val364CysfsTer6)
n.2179_2180insA
c.892_893insA
c.621_622insA
c.1088_1089insA
c.1346_1347insA (p.Val450CysfsTer6)
n.1134_1135insA
c.942_943insA
ClinVar dbSNP
2g.32137138T>ACA425449191SPASTc.*1103T>A (n.*1103T>A)
c.1443T>A (p.Leu481=)
c.1440T>A (p.Leu480=)
c.1180T>A
c.1344T>A (p.Leu448=)
c.1217T>A
c.1185T>A (p.Leu395=)
c.510T>A
c.1023T>A
c.1319T>A
c.1089T>A (p.Leu363=)
n.2180T>A
c.893T>A
c.622T>A
c.1089T>A
c.1347T>A (p.Leu449=)
n.1135T>A
c.943T>A
2g.32137138T>CCA425449190SPASTc.*1103T>C (n.*1103T>C)
c.1443T>C (p.Leu481=)
c.1440T>C (p.Leu480=)
c.1180T>C
c.1344T>C (p.Leu448=)
c.1217T>C
c.1185T>C (p.Leu395=)
c.510T>C
c.1023T>C
c.1319T>C
c.1089T>C (p.Leu363=)
n.2180T>C
c.893T>C
c.622T>C
c.1089T>C
c.1347T>C (p.Leu449=)
n.1135T>C
c.943T>C
2g.32137138T>GCA425449189SPASTc.*1103T>G (n.*1103T>G)
c.1443T>G (p.Leu481=)
c.1440T>G (p.Leu480=)
c.1180T>G
c.1344T>G (p.Leu448=)
c.1217T>G
c.1185T>G (p.Leu395=)
c.510T>G
c.1023T>G
c.1319T>G
c.1089T>G (p.Leu363=)
n.2180T>G
c.893T>G
c.622T>G
c.1089T>G
c.1347T>G (p.Leu449=)
n.1135T>G
c.943T>G
2g.32137139G>ACA346502441SPASTc.*1104G>A (n.*1104G>A)
c.1444G>A (p.Val482Ile)
c.1441G>A (p.Val481Ile)
c.1181G>A
c.1345G>A (p.Val449Ile)
c.1218G>A
c.1186G>A (p.Val396Ile)
c.511G>A
c.1024G>A
c.1320G>A
c.1090G>A (p.Val364Ile)
n.2181G>A
c.894G>A
c.623G>A
c.1090G>A
c.1348G>A (p.Val450Ile)
n.1136G>A
c.944G>A
gnomAD v4
2g.32137139G>CCA346502442SPASTc.*1104G>C (n.*1104G>C)
c.1444G>C (p.Val482Leu)
c.1441G>C (p.Val481Leu)
c.1181G>C
c.1345G>C (p.Val449Leu)
c.1218G>C
c.1186G>C (p.Val396Leu)
c.511G>C
c.1024G>C
c.1320G>C
c.1090G>C (p.Val364Leu)
n.2181G>C
c.894G>C
c.623G>C
c.1090G>C
c.1348G>C (p.Val450Leu)
n.1136G>C
c.944G>C
dbSNP
2g.32137139G=CA1242502056SPASTc.*1104G= (n.*1104G=)
c.1444G= (p.Val482=)
c.1441G= (p.Val481=)
c.1181G=
c.1345G= (p.Val449=)
c.1218G=
c.1186G= (p.Val396=)
c.511G=
c.1024G=
c.1320G=
c.1090G= (p.Val364=)
n.2181G=
c.894G=
c.623G=
c.1090G=
c.1348G= (p.Val450=)
n.1136G=
c.944G=
2g.32137139G>TCA346502443SPASTc.*1104G>T (n.*1104G>T)
c.1444G>T (p.Val482Leu)
c.1441G>T (p.Val481Leu)
c.1181G>T
c.1345G>T (p.Val449Leu)
c.1218G>T
c.1186G>T (p.Val396Leu)
c.511G>T
c.1024G>T
c.1320G>T
c.1090G>T (p.Val364Leu)
n.2181G>T
c.894G>T
c.623G>T
c.1090G>T
c.1348G>T (p.Val450Leu)
n.1136G>T
c.944G>T
2g.32137140T>ACA346502444SPASTc.*1105T>A (n.*1105T>A)
c.1445T>A (p.Val482Glu)
c.1442T>A (p.Val481Glu)
c.1182T>A
c.1346T>A (p.Val449Glu)
c.1219T>A
c.1187T>A (p.Val396Glu)
c.512T>A
c.1025T>A
c.1321T>A
c.1091T>A (p.Val364Glu)
n.2182T>A
c.895T>A
c.624T>A
c.1091T>A
c.1349T>A (p.Val450Glu)
n.1137T>A
c.945T>A
2g.32137140T>CCA346502445SPASTc.*1105T>C (n.*1105T>C)
c.1445T>C (p.Val482Ala)
c.1442T>C (p.Val481Ala)
c.1182T>C
c.1346T>C (p.Val449Ala)
c.1219T>C
c.1187T>C (p.Val396Ala)
c.512T>C
c.1025T>C
c.1321T>C
c.1091T>C (p.Val364Ala)
n.2182T>C
c.895T>C
c.624T>C
c.1091T>C
c.1349T>C (p.Val450Ala)
n.1137T>C
c.945T>C
ClinVar dbSNP gnomAD v2 gnomAD v4
2g.32137140T>GCA346502446SPASTc.*1105T>G (n.*1105T>G)
c.1445T>G (p.Val482Gly)
c.1442T>G (p.Val481Gly)
c.1182T>G
c.1346T>G (p.Val449Gly)
c.1219T>G
c.1187T>G (p.Val396Gly)
c.512T>G
c.1025T>G
c.1321T>G
c.1091T>G (p.Val364Gly)
n.2182T>G
c.895T>G
c.624T>G
c.1091T>G
c.1349T>G (p.Val450Gly)
n.1137T>G
c.945T>G
2g.32137140T=CA1242502059SPASTc.*1105T= (n.*1105T=)
c.1445T= (p.Val482=)
c.1442T= (p.Val481=)
c.1182T=
c.1346T= (p.Val449=)
c.1219T=
c.1187T= (p.Val396=)
c.512T=
c.1025T=
c.1321T=
c.1091T= (p.Val364=)
n.2182T=
c.895T=
c.624T=
c.1091T=
c.1349T= (p.Val450=)
n.1137T=
c.945T=
2g.32137141A=CA1242502063SPASTc.*1106A= (n.*1106A=)
c.1446A= (p.Val482=)
c.1443A= (p.Val481=)
c.1183A=
c.1347A= (p.Val449=)
c.1220A=
c.1188A= (p.Val396=)
c.513A=
c.1026A=
c.1322A=
c.1092A= (p.Val364=)
n.2183A=
c.896A=
c.625A=
c.1092A=
c.1350A= (p.Val450=)
n.1138A=
c.946A=
2g.32137141A>CCA425449192SPASTc.*1106A>C (n.*1106A>C)
c.1446A>C (p.Val482=)
c.1443A>C (p.Val481=)
c.1183A>C
c.1347A>C (p.Val449=)
c.1220A>C
c.1188A>C (p.Val396=)
c.513A>C
c.1026A>C
c.1322A>C
c.1092A>C (p.Val364=)
n.2183A>C
c.896A>C
c.625A>C
c.1092A>C
c.1350A>C (p.Val450=)
n.1138A>C
c.946A>C
dbSNP
2g.32137141A>GCA425449193SPASTc.*1106A>G (n.*1106A>G)
c.1446A>G (p.Val482=)
c.1443A>G (p.Val481=)
c.1183A>G
c.1347A>G (p.Val449=)
c.1220A>G
c.1188A>G (p.Val396=)
c.513A>G
c.1026A>G
c.1322A>G
c.1092A>G (p.Val364=)
n.2183A>G
c.896A>G
c.625A>G
c.1092A>G
c.1350A>G (p.Val450=)
n.1138A>G
c.946A>G
2g.32137141A>TCA425449194SPASTc.*1106A>T (n.*1106A>T)
c.1446A>T (p.Val482=)
c.1443A>T (p.Val481=)
c.1183A>T
c.1347A>T (p.Val449=)
c.1220A>T
c.1188A>T (p.Val396=)
c.513A>T
c.1026A>T
c.1322A>T
c.1092A>T (p.Val364=)
n.2183A>T
c.896A>T
c.625A>T
c.1092A>T
c.1350A>T (p.Val450=)
n.1138A>T
c.946A>T
2g.32137142A>CCA346502447SPASTc.*1107A>C (n.*1107A>C)
c.1447A>C (p.Met483Leu)
c.1444A>C (p.Met482Leu)
c.1184A>C
c.1348A>C (p.Met450Leu)
c.1221A>C
c.1189A>C (p.Met397Leu)
c.514A>C
c.1027A>C
c.1323A>C
c.1093A>C (p.Met365Leu)
n.2184A>C
c.897A>C
c.626A>C
c.1093A>C
c.1351A>C (p.Met451Leu)
n.1139A>C
c.947A>C
2g.32137142A>GCA346502448SPASTc.*1107A>G (n.*1107A>G)
c.1447A>G (p.Met483Val)
c.1444A>G (p.Met482Val)
c.1184A>G
c.1348A>G (p.Met450Val)
c.1221A>G
c.1189A>G (p.Met397Val)
c.514A>G
c.1027A>G
c.1323A>G
c.1093A>G (p.Met365Val)
n.2184A>G
c.897A>G
c.626A>G
c.1093A>G
c.1351A>G (p.Met451Val)
n.1139A>G
c.947A>G
2g.32137142A>TCA346502449SPASTc.*1107A>T (n.*1107A>T)
c.1447A>T (p.Met483Leu)
c.1444A>T (p.Met482Leu)
c.1184A>T
c.1348A>T (p.Met450Leu)
c.1221A>T
c.1189A>T (p.Met397Leu)
c.514A>T
c.1027A>T
c.1323A>T
c.1093A>T (p.Met365Leu)
n.2184A>T
c.897A>T
c.626A>T
c.1093A>T
c.1351A>T (p.Met451Leu)
n.1139A>T
c.947A>T
2g.32137142_32137143delCA2586964778SPASTc.*1107_*1108del (n.*1107_*1108del)
c.1447_1448del (p.Met483GlyfsTer4)
c.1444_1445del (p.Met482GlyfsTer4)
c.1184_1185del
c.1348_1349del (p.Met450GlyfsTer4)
c.1221_1222del
c.1189_1190del (p.Met397GlyfsTer4)
c.514_515del
c.1027_1028del
c.1323_1324del
c.1093_1094del (p.Met365GlyfsTer4)
n.2184_2185del
c.897_898del
c.626_627del
c.1093_1094del
c.1351_1352del (p.Met451GlyfsTer4)
n.1139_1140del
c.947_948del
2g.32137143T>ACA346502452SPASTc.*1108T>A (n.*1108T>A)
c.1448T>A (p.Met483Lys)
c.1445T>A (p.Met482Lys)
c.1185T>A
c.1349T>A (p.Met450Lys)
c.1222T>A
c.1190T>A (p.Met397Lys)
c.515T>A
c.1028T>A
c.1324T>A
c.1094T>A (p.Met365Lys)
n.2185T>A
c.898T>A
c.627T>A
c.1094T>A
c.1352T>A (p.Met451Lys)
n.1140T>A
c.948T>A
2g.32137143T>CCA346502450SPASTc.*1108T>C (n.*1108T>C)
c.1448T>C (p.Met483Thr)
c.1445T>C (p.Met482Thr)
c.1185T>C
c.1349T>C (p.Met450Thr)
c.1222T>C
c.1190T>C (p.Met397Thr)
c.515T>C
c.1028T>C
c.1324T>C
c.1094T>C (p.Met365Thr)
n.2185T>C
c.898T>C
c.627T>C
c.1094T>C
c.1352T>C (p.Met451Thr)
n.1140T>C
c.948T>C
ClinVar dbSNP
2g.32137143T>GCA346502451SPASTc.*1108T>G (n.*1108T>G)
c.1448T>G (p.Met483Arg)
c.1445T>G (p.Met482Arg)
c.1185T>G
c.1349T>G (p.Met450Arg)
c.1222T>G
c.1190T>G (p.Met397Arg)
c.515T>G
c.1028T>G
c.1324T>G
c.1094T>G (p.Met365Arg)
n.2185T>G
c.898T>G
c.627T>G
c.1094T>G
c.1352T>G (p.Met451Arg)
n.1140T>G
c.948T>G
ClinVar
2g.32137143T=CA1242502068SPASTc.*1108T= (n.*1108T=)
c.1448T= (p.Met483=)
c.1445T= (p.Met482=)
c.1185T=
c.1349T= (p.Met450=)
c.1222T=
c.1190T= (p.Met397=)
c.515T=
c.1028T=
c.1324T=
c.1094T= (p.Met365=)
n.2185T=
c.898T=
c.627T=
c.1094T=
c.1352T= (p.Met451=)
n.1140T=
c.948T=
2g.32137143_32137144delinsTGCA1242502070SPASTc.*1108_*1109delinsTG (n.*1108_*1109delinsTG)
c.1448_1449delinsTG (p.Met483=)
c.1445_1446delinsTG (p.Met482=)
c.1185_1186delinsTG
c.1349_1350delinsTG (p.Met450=)
c.1222_1223delinsTG
c.1190_1191delinsTG (p.Met397=)
c.515_516delinsTG
c.1028_1029delinsTG
c.1324_1325delinsTG
c.1094_1095delinsTG (p.Met365=)
n.2185_2186delinsTG
c.898_899delinsTG
c.627_628delinsTG
c.1094_1095delinsTG
c.1352_1353delinsTG (p.Met451=)
n.1140_1141delinsTG
c.948_949delinsTG
2g.32137144G>ACA346502453SPASTc.*1109G>A (n.*1109G>A)
c.1449G>A (p.Met483Ile)
c.1446G>A (p.Met482Ile)
c.1186G>A
c.1350G>A (p.Met450Ile)
c.1223G>A
c.1191G>A (p.Met397Ile)
c.516G>A
c.1029G>A
c.1325G>A
c.1095G>A (p.Met365Ile)
n.2186G>A
c.899G>A
c.628G>A
c.1095G>A
c.1353G>A (p.Met451Ile)
n.1141G>A
c.949G>A
2g.32137144G>CCA346502454SPASTc.*1109G>C (n.*1109G>C)
c.1449G>C (p.Met483Ile)
c.1446G>C (p.Met482Ile)
c.1186G>C
c.1350G>C (p.Met450Ile)
c.1223G>C
c.1191G>C (p.Met397Ile)
c.516G>C
c.1029G>C
c.1325G>C
c.1095G>C (p.Met365Ile)
n.2186G>C
c.899G>C
c.628G>C
c.1095G>C
c.1353G>C (p.Met451Ile)
n.1141G>C
c.949G>C
2g.32137144G>TCA346502455SPASTc.*1109G>T (n.*1109G>T)
c.1449G>T (p.Met483Ile)
c.1446G>T (p.Met482Ile)
c.1186G>T
c.1350G>T (p.Met450Ile)
c.1223G>T
c.1191G>T (p.Met397Ile)
c.516G>T
c.1029G>T
c.1325G>T
c.1095G>T (p.Met365Ile)
n.2186G>T
c.899G>T
c.628G>T
c.1095G>T
c.1353G>T (p.Met451Ile)
n.1141G>T
c.949G>T
2g.32137146delCA1242502073SPASTc.*1111del (n.*1111del)
c.1451del (p.Gly484ValfsTer?)
c.1448del (p.Gly483ValfsTer?)
c.1188del
c.1352del (p.Gly451ValfsTer?)
c.1225del
c.1193del (p.Gly398ValfsTer?)
c.518del
c.1031del
c.1327del
c.1097del (p.Gly366ValfsTer?)
n.2188del
c.901del
c.630del
c.1097del
c.1355del (p.Gly452ValfsTer?)
n.1143del
c.951del
dbSNP
2g.32137145_32137146delCA2586964779SPASTc.*1110_*1111del (n.*1110_*1111del)
c.1450_1451del (p.Gly484CysfsTer3)
c.1447_1448del (p.Gly483CysfsTer3)
c.1187_1188del
c.1351_1352del (p.Gly451CysfsTer3)
c.1224_1225del
c.1192_1193del (p.Gly398CysfsTer3)
c.517_518del
c.1030_1031del
c.1326_1327del
c.1096_1097del (p.Gly366CysfsTer3)
n.2187_2188del
c.900_901del
c.629_630del
c.1096_1097del
c.1354_1355del (p.Gly452CysfsTer3)
n.1142_1143del
c.950_951del
2g.32137145G>ACA346502456SPASTc.*1110G>A (n.*1110G>A)
c.1450G>A (p.Gly484Ser)
c.1447G>A (p.Gly483Ser)
c.1187G>A
c.1351G>A (p.Gly451Ser)
c.1224G>A
c.1192G>A (p.Gly398Ser)
c.517G>A
c.1030G>A
c.1326G>A
c.1096G>A (p.Gly366Ser)
n.2187G>A
c.900G>A
c.629G>A
c.1096G>A
c.1354G>A (p.Gly452Ser)
n.1142G>A
c.950G>A
2g.32137145G>CCA346502457SPASTc.*1110G>C (n.*1110G>C)
c.1450G>C (p.Gly484Arg)
c.1447G>C (p.Gly483Arg)
c.1187G>C
c.1351G>C (p.Gly451Arg)
c.1224G>C
c.1192G>C (p.Gly398Arg)
c.517G>C
c.1030G>C
c.1326G>C
c.1096G>C (p.Gly366Arg)
n.2187G>C
c.900G>C
c.629G>C
c.1096G>C
c.1354G>C (p.Gly452Arg)
n.1142G>C
c.950G>C
ClinVar dbSNP
2g.32137145G=CA1242502076SPASTc.*1110G= (n.*1110G=)
c.1450G= (p.Gly484=)
c.1447G= (p.Gly483=)
c.1187G=
c.1351G= (p.Gly451=)
c.1224G=
c.1192G= (p.Gly398=)
c.517G=
c.1030G=
c.1326G=
c.1096G= (p.Gly366=)
n.2187G=
c.900G=
c.629G=
c.1096G=
c.1354G= (p.Gly452=)
n.1142G=
c.950G=
2g.32137145G>TCA346502458SPASTc.*1110G>T (n.*1110G>T)
c.1450G>T (p.Gly484Cys)
c.1447G>T (p.Gly483Cys)
c.1187G>T
c.1351G>T (p.Gly451Cys)
c.1224G>T
c.1192G>T (p.Gly398Cys)
c.517G>T
c.1030G>T
c.1326G>T
c.1096G>T (p.Gly366Cys)
n.2187G>T
c.900G>T
c.629G>T
c.1096G>T
c.1354G>T (p.Gly452Cys)
n.1142G>T
c.950G>T
2g.32137146G>ACA346502459SPASTc.*1111G>A (n.*1111G>A)
c.1451G>A (p.Gly484Asp)
c.1448G>A (p.Gly483Asp)
c.1188G>A
c.1352G>A (p.Gly451Asp)
c.1225G>A
c.1193G>A (p.Gly398Asp)
c.518G>A
c.1031G>A
c.1327G>A
c.1097G>A (p.Gly366Asp)
n.2188G>A
c.901G>A
c.630G>A
c.1097G>A
c.1355G>A (p.Gly452Asp)
n.1143G>A
c.951G>A
ClinVar dbSNP
2g.32137146G>CCA346502460SPASTc.*1111G>C (n.*1111G>C)
c.1451G>C (p.Gly484Ala)
c.1448G>C (p.Gly483Ala)
c.1188G>C
c.1352G>C (p.Gly451Ala)
c.1225G>C
c.1193G>C (p.Gly398Ala)
c.518G>C
c.1031G>C
c.1327G>C
c.1097G>C (p.Gly366Ala)
n.2188G>C
c.901G>C
c.630G>C
c.1097G>C
c.1355G>C (p.Gly452Ala)
n.1143G>C
c.951G>C
2g.32137146G=CA1242502086SPASTc.*1111G= (n.*1111G=)
c.1451G= (p.Gly484=)
c.1448G= (p.Gly483=)
c.1188G=
c.1352G= (p.Gly451=)
c.1225G=
c.1193G= (p.Gly398=)
c.518G=
c.1031G=
c.1327G=
c.1097G= (p.Gly366=)
n.2188G=
c.901G=
c.630G=
c.1097G=
c.1355G= (p.Gly452=)
n.1143G=
c.951G=
2g.32137146G>TCA346502461SPASTc.*1111G>T (n.*1111G>T)
c.1451G>T (p.Gly484Val)
c.1448G>T (p.Gly483Val)
c.1188G>T
c.1352G>T (p.Gly451Val)
c.1225G>T
c.1193G>T (p.Gly398Val)
c.518G>T
c.1031G>T
c.1327G>T
c.1097G>T (p.Gly366Val)
n.2188G>T
c.901G>T
c.630G>T
c.1097G>T
c.1355G>T (p.Gly452Val)
n.1143G>T
c.951G>T
2g.32137147T>ACA425449195SPASTc.*1112T>A (n.*1112T>A)
c.1452T>A (p.Gly484=)
c.1449T>A (p.Gly483=)
c.1189T>A
c.1353T>A (p.Gly451=)
c.1226T>A
c.1194T>A (p.Gly398=)
c.519T>A
c.1032T>A
c.1328T>A
c.1098T>A (p.Gly366=)
n.2189T>A
c.902T>A
c.631T>A
c.1098T>A
c.1356T>A (p.Gly452=)
n.1144T>A
c.952T>A
2g.32137147T>CCA425449196SPASTc.*1112T>C (n.*1112T>C)
c.1452T>C (p.Gly484=)
c.1449T>C (p.Gly483=)
c.1189T>C
c.1353T>C (p.Gly451=)
c.1226T>C
c.1194T>C (p.Gly398=)
c.519T>C
c.1032T>C
c.1328T>C
c.1098T>C (p.Gly366=)
n.2189T>C
c.902T>C
c.631T>C
c.1098T>C
c.1356T>C (p.Gly452=)
n.1144T>C
c.952T>C
dbSNP gnomAD v2
2g.32137147T>GCA425449197SPASTc.*1112T>G (n.*1112T>G)
c.1452T>G (p.Gly484=)
c.1449T>G (p.Gly483=)
c.1189T>G
c.1353T>G (p.Gly451=)
c.1226T>G
c.1194T>G (p.Gly398=)
c.519T>G
c.1032T>G
c.1328T>G
c.1098T>G (p.Gly366=)
n.2189T>G
c.902T>G
c.631T>G
c.1098T>G
c.1356T>G (p.Gly452=)
n.1144T>G
c.952T>G
2g.32137147T=CA1242502095SPASTc.*1112T= (n.*1112T=)
c.1452T= (p.Gly484=)
c.1449T= (p.Gly483=)
c.1189T=
c.1353T= (p.Gly451=)
c.1226T=
c.1194T= (p.Gly398=)
c.519T=
c.1032T=
c.1328T=
c.1098T= (p.Gly366=)
n.2189T=
c.902T=
c.631T=
c.1098T=
c.1356T= (p.Gly452=)
n.1144T=
c.952T=

Number of alleles fetched