| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.32140511_32146752dup | CA10575835 | SPAST | c.*1154-1393_*1348-466dup c.1494-1393_1688-466dup c.1491-1393_1685-466dup c.1231-1393_1425-466dup c.1395-1393_1589-466dup c.1268-1393_1391-466dup c.1236-1393_1430-466dup c.1074-1393_1268-466dup c.1370-1393_1564-443dup c.1140-1393_1334-466dup n.2231-1393_2425-466dup c.944-1393_1067-466dup c.673-1393_867-466dup c.1398-1393_1592-466dup n.1186-1393_1380-466dup c.994-1393_1188-466dup c.1494-1393_1617-466dup c.1398-1393_1521-466dup | |
| 2 | g.32141902_32141906del | CA1029035975 | SPAST | c.*1154-2_*1156del c.1494-2_1496del c.1491-2_1493del c.1231-2_1233del c.1395-2_1397del c.1268-2_1270del c.1236-2_1238del c.561-2_563del c.1074-2_1076del c.1370-2_1372del c.1140-2_1142del n.2231-2_2233del c.944-2_946del c.673-2_675del c.1398-2_1400del n.1186-2_1188del c.994-2_996del | gnomAD v4 |
| 2 | g.32141905C>A | CA346502822 | SPAST | c.*1155C>A (n.*1155C>A) c.1495C>A (p.Arg499Ser) c.1492C>A (p.Arg498Ser) c.1232C>A c.1396C>A (p.Arg466Ser) c.1269C>A c.1237C>A (p.Arg413Ser) c.562C>A c.1075C>A c.1371C>A c.1141C>A (p.Arg381Ser) n.2232C>A c.945C>A c.674C>A c.1141C>A c.1399C>A (p.Arg467Ser) n.1187C>A c.995C>A | ClinVar dbSNP gnomAD v4 |
| 2 | g.32141905C= | CA1242504512 | SPAST | c.*1155C= (n.*1155C=) c.1495C= (p.Arg499=) c.1492C= (p.Arg498=) c.1232C= c.1396C= (p.Arg466=) c.1269C= c.1237C= (p.Arg413=) c.562C= c.1075C= c.1371C= c.1141C= (p.Arg381=) n.2232C= c.945C= c.674C= c.1141C= c.1399C= (p.Arg467=) n.1187C= c.995C= | |
| 2 | g.32141905C>G | CA346502820 | SPAST | c.*1155C>G (n.*1155C>G) c.1495C>G (p.Arg499Gly) c.1492C>G (p.Arg498Gly) c.1232C>G c.1396C>G (p.Arg466Gly) c.1269C>G c.1237C>G (p.Arg413Gly) c.562C>G c.1075C>G c.1371C>G c.1141C>G (p.Arg381Gly) n.2232C>G c.945C>G c.674C>G c.1141C>G c.1399C>G (p.Arg467Gly) n.1187C>G c.995C>G | |
| 2 | g.32141905C>T | CA253551 | SPAST | c.*1155C>T (n.*1155C>T) c.1495C>T (p.Arg499Cys) c.1492C>T (p.Arg498Cys) c.1232C>T c.1396C>T (p.Arg466Cys) c.1269C>T c.1237C>T (p.Arg413Cys) c.562C>T c.1075C>T c.1371C>T c.1141C>T (p.Arg381Cys) n.2232C>T c.945C>T c.674C>T c.1141C>T c.1399C>T (p.Arg467Cys) n.1187C>T c.995C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 2 | g.32141906del | CA2499215911 | SPAST | c.*1156del (n.*1156del) c.1496del (p.Arg499LeufsTer?) c.1493del (p.Arg498LeufsTer?) c.1233del c.1397del (p.Arg466LeufsTer?) c.1270del c.1238del (p.Arg413LeufsTer?) c.563del c.1076del c.1372del c.1142del (p.Arg381LeufsTer?) n.2233del c.946del c.675del c.1142del c.1400del (p.Arg467LeufsTer?) n.1188del c.996del | ClinVar dbSNP |
| 2 | g.32141906G>A | CA10581969 | SPAST | c.*1156G>A (n.*1156G>A) c.1496G>A (p.Arg499His) c.1493G>A (p.Arg498His) c.1233G>A c.1397G>A (p.Arg466His) c.1270G>A c.1238G>A (p.Arg413His) c.563G>A c.1076G>A c.1372G>A c.1142G>A (p.Arg381His) n.2233G>A c.946G>A c.675G>A c.1142G>A c.1400G>A (p.Arg467His) n.1188G>A c.996G>A | ClinVar dbSNP gnomAD v4 |
| 2 | g.32141906G>C | CA346502825 | SPAST | c.*1156G>C (n.*1156G>C) c.1496G>C (p.Arg499Pro) c.1493G>C (p.Arg498Pro) c.1233G>C c.1397G>C (p.Arg466Pro) c.1270G>C c.1238G>C (p.Arg413Pro) c.563G>C c.1076G>C c.1372G>C c.1142G>C (p.Arg381Pro) n.2233G>C c.946G>C c.675G>C c.1142G>C c.1400G>C (p.Arg467Pro) n.1188G>C c.996G>C | |
| 2 | g.32141906G= | CA1242504513 | SPAST | c.*1156G= (n.*1156G=) c.1496G= (p.Arg499=) c.1493G= (p.Arg498=) c.1233G= c.1397G= (p.Arg466=) c.1270G= c.1238G= (p.Arg413=) c.563G= c.1076G= c.1372G= c.1142G= (p.Arg381=) n.2233G= c.946G= c.675G= c.1142G= c.1400G= (p.Arg467=) n.1188G= c.996G= | |
| 2 | g.32141906G>T | CA346502827 | SPAST | c.*1156G>T (n.*1156G>T) c.1496G>T (p.Arg499Leu) c.1493G>T (p.Arg498Leu) c.1233G>T c.1397G>T (p.Arg466Leu) c.1270G>T c.1238G>T (p.Arg413Leu) c.563G>T c.1076G>T c.1372G>T c.1142G>T (p.Arg381Leu) n.2233G>T c.946G>T c.675G>T c.1142G>T c.1400G>T (p.Arg467Leu) n.1188G>T c.996G>T | ClinVar dbSNP gnomAD v4 |
| 2 | g.32141907T>A | CA425451025 | SPAST | c.*1157T>A (n.*1157T>A) c.1497T>A (p.Arg499=) c.1494T>A (p.Arg498=) c.1234T>A c.1398T>A (p.Arg466=) c.1271T>A c.1239T>A (p.Arg413=) c.564T>A c.1077T>A c.1373T>A c.1143T>A (p.Arg381=) n.2234T>A c.947T>A c.676T>A c.1143T>A c.1401T>A (p.Arg467=) n.1189T>A c.997T>A | |
| 2 | g.32141907T>C | CA425451026 | SPAST | c.*1157T>C (n.*1157T>C) c.1497T>C (p.Arg499=) c.1494T>C (p.Arg498=) c.1234T>C c.1398T>C (p.Arg466=) c.1271T>C c.1239T>C (p.Arg413=) c.564T>C c.1077T>C c.1373T>C c.1143T>C (p.Arg381=) n.2234T>C c.947T>C c.676T>C c.1143T>C c.1401T>C (p.Arg467=) n.1189T>C c.997T>C | |
| 2 | g.32141907T>G | CA425451036 | SPAST | c.*1157T>G (n.*1157T>G) c.1497T>G (p.Arg499=) c.1494T>G (p.Arg498=) c.1234T>G c.1398T>G (p.Arg466=) c.1271T>G c.1239T>G (p.Arg413=) c.564T>G c.1077T>G c.1373T>G c.1143T>G (p.Arg381=) n.2234T>G c.947T>G c.676T>G c.1143T>G c.1401T>G (p.Arg467=) n.1189T>G c.997T>G | |
| 2 | g.32141909_32141910insTTTTT | CA1029035982 | SPAST | c.*1159_*1160insTTTTT (n.*1159_*1160insTTTTT) c.1499_1500insTTTTT (p.Ile501PhefsTer31) c.1496_1497insTTTTT (p.Ile500PhefsTer31) c.1236_1237insTTTTT c.1400_1401insTTTTT (p.Ile468PhefsTer31) c.1273_1274insTTTTT c.1241_1242insTTTTT (p.Ile415PhefsTer31) c.566_567insTTTTT c.1079_1080insTTTTT c.1375_1376insTTTTT c.1145_1146insTTTTT (p.Ile383PhefsTer31) n.2236_2237insTTTTT c.949_950insTTTTT c.678_679insTTTTT c.1145_1146insTTTTT c.1403_1404insTTTTT (p.Ile469PhefsTer31) n.1191_1192insTTTTT c.999_1000insTTTTT | |
| 2 | g.32141908T>A | CA346502829 | SPAST | c.*1158T>A (n.*1158T>A) c.1498T>A (p.Phe500Ile) c.1495T>A (p.Phe499Ile) c.1235T>A c.1399T>A (p.Phe467Ile) c.1272T>A c.1240T>A (p.Phe414Ile) c.565T>A c.1078T>A c.1374T>A c.1144T>A (p.Phe382Ile) n.2235T>A c.948T>A c.677T>A c.1144T>A c.1402T>A (p.Phe468Ile) n.1190T>A c.998T>A | |
| 2 | g.32141908T>C | CA346502831 | SPAST | c.*1158T>C (n.*1158T>C) c.1498T>C (p.Phe500Leu) c.1495T>C (p.Phe499Leu) c.1235T>C c.1399T>C (p.Phe467Leu) c.1272T>C c.1240T>C (p.Phe414Leu) c.565T>C c.1078T>C c.1374T>C c.1144T>C (p.Phe382Leu) n.2235T>C c.948T>C c.677T>C c.1144T>C c.1402T>C (p.Phe468Leu) n.1190T>C c.998T>C | |
| 2 | g.32141908T>G | CA346502832 | SPAST | c.*1158T>G (n.*1158T>G) c.1498T>G (p.Phe500Val) c.1495T>G (p.Phe499Val) c.1235T>G c.1399T>G (p.Phe467Val) c.1272T>G c.1240T>G (p.Phe414Val) c.565T>G c.1078T>G c.1374T>G c.1144T>G (p.Phe382Val) n.2235T>G c.948T>G c.677T>G c.1144T>G c.1402T>G (p.Phe468Val) n.1190T>G c.998T>G | |
| 2 | g.32141909T>A | CA346502834 | SPAST | c.*1159T>A (n.*1159T>A) c.1499T>A (p.Phe500Tyr) c.1496T>A (p.Phe499Tyr) c.1236T>A c.1400T>A (p.Phe467Tyr) c.1273T>A c.1241T>A (p.Phe414Tyr) c.566T>A c.1079T>A c.1375T>A c.1145T>A (p.Phe382Tyr) n.2236T>A c.949T>A c.678T>A c.1145T>A c.1403T>A (p.Phe468Tyr) n.1191T>A c.999T>A | |
| 2 | g.32141909T>C | CA346502838 | SPAST | c.*1159T>C (n.*1159T>C) c.1499T>C (p.Phe500Ser) c.1496T>C (p.Phe499Ser) c.1236T>C c.1400T>C (p.Phe467Ser) c.1273T>C c.1241T>C (p.Phe414Ser) c.566T>C c.1079T>C c.1375T>C c.1145T>C (p.Phe382Ser) n.2236T>C c.949T>C c.678T>C c.1145T>C c.1403T>C (p.Phe468Ser) n.1191T>C c.999T>C | gnomAD v4 |
| 2 | g.32141909T>G | CA346502836 | SPAST | c.*1159T>G (n.*1159T>G) c.1499T>G (p.Phe500Cys) c.1496T>G (p.Phe499Cys) c.1236T>G c.1400T>G (p.Phe467Cys) c.1273T>G c.1241T>G (p.Phe414Cys) c.566T>G c.1079T>G c.1375T>G c.1145T>G (p.Phe382Cys) n.2236T>G c.949T>G c.678T>G c.1145T>G c.1403T>G (p.Phe468Cys) n.1191T>G c.999T>G | ClinVar dbSNP |
| 2 | g.32141909T= | CA1242504514 | SPAST | c.*1159T= (n.*1159T=) c.1499T= (p.Phe500=) c.1496T= (p.Phe499=) c.1236T= c.1400T= (p.Phe467=) c.1273T= c.1241T= (p.Phe414=) c.566T= c.1079T= c.1375T= c.1145T= (p.Phe382=) n.2236T= c.949T= c.678T= c.1145T= c.1403T= (p.Phe468=) n.1191T= c.999T= | |
| 2 | g.32141910C>A | CA346502839 | SPAST | c.*1160C>A (n.*1160C>A) c.1500C>A (p.Phe500Leu) c.1497C>A (p.Phe499Leu) c.1237C>A c.1401C>A (p.Phe467Leu) c.1274C>A c.1242C>A (p.Phe414Leu) c.567C>A c.1080C>A c.1376C>A c.1146C>A (p.Phe382Leu) n.2237C>A c.950C>A c.679C>A c.1146C>A c.1404C>A (p.Phe468Leu) n.1192C>A c.1000C>A | gnomAD v4 |
| 2 | g.32141910C>G | CA346502840 | SPAST | c.*1160C>G (n.*1160C>G) c.1500C>G (p.Phe500Leu) c.1497C>G (p.Phe499Leu) c.1237C>G c.1401C>G (p.Phe467Leu) c.1274C>G c.1242C>G (p.Phe414Leu) c.567C>G c.1080C>G c.1376C>G c.1146C>G (p.Phe382Leu) n.2237C>G c.950C>G c.679C>G c.1146C>G c.1404C>G (p.Phe468Leu) n.1192C>G c.1000C>G | ClinVar |
| 2 | g.32141910C>T | CA425451053 | SPAST | c.*1160C>T (n.*1160C>T) c.1500C>T (p.Phe500=) c.1497C>T (p.Phe499=) c.1237C>T c.1401C>T (p.Phe467=) c.1274C>T c.1242C>T (p.Phe414=) c.567C>T c.1080C>T c.1376C>T c.1146C>T (p.Phe382=) n.2237C>T c.950C>T c.679C>T c.1146C>T c.1404C>T (p.Phe468=) n.1192C>T c.1000C>T | |
| 2 | g.32141910_32141911insT | CA2586968961 | SPAST | c.*1160_*1161insT (n.*1160_*1161insT) c.1500_1501insT (p.Ile501TyrfsTer11) c.1497_1498insT (p.Ile500TyrfsTer11) c.1237_1238insT c.1401_1402insT (p.Ile468TyrfsTer11) c.1274_1275insT c.1242_1243insT (p.Ile415TyrfsTer11) c.567_568insT c.1080_1081insT c.1376_1377insT c.1146_1147insT (p.Ile383TyrfsTer11) n.2237_2238insT c.950_951insT c.679_680insT c.1146_1147insT c.1404_1405insT (p.Ile469TyrfsTer11) n.1192_1193insT c.1000_1001insT | |
| 2 | g.32141911A= | CA1242504515 | SPAST | c.*1161A= (n.*1161A=) c.1501A= (p.Ile501=) c.1498A= (p.Ile500=) c.1238A= c.1402A= (p.Ile468=) c.1275A= c.1243A= (p.Ile415=) c.568A= c.1081A= c.1377A= c.1147A= (p.Ile383=) n.2238A= c.951A= c.680A= c.1147A= c.1405A= (p.Ile469=) n.1193A= c.1001A= | |
| 2 | g.32141911A>C | CA16043744 | SPAST | c.*1161A>C (n.*1161A>C) c.1501A>C (p.Ile501Leu) c.1498A>C (p.Ile500Leu) c.1238A>C c.1402A>C (p.Ile468Leu) c.1275A>C c.1243A>C (p.Ile415Leu) c.568A>C c.1081A>C c.1377A>C c.1147A>C (p.Ile383Leu) n.2238A>C c.951A>C c.680A>C c.1147A>C c.1405A>C (p.Ile469Leu) n.1193A>C c.1001A>C | ClinVar dbSNP |
| 2 | g.32141911A>G | CA346502842 | SPAST | c.*1161A>G (n.*1161A>G) c.1501A>G (p.Ile501Val) c.1498A>G (p.Ile500Val) c.1238A>G c.1402A>G (p.Ile468Val) c.1275A>G c.1243A>G (p.Ile415Val) c.568A>G c.1081A>G c.1377A>G c.1147A>G (p.Ile383Val) n.2238A>G c.951A>G c.680A>G c.1147A>G c.1405A>G (p.Ile469Val) n.1193A>G c.1001A>G | gnomAD v4 COSMIC |
| 2 | g.32141911A>T | CA346502844 | SPAST | c.*1161A>T (n.*1161A>T) c.1501A>T (p.Ile501Phe) c.1498A>T (p.Ile500Phe) c.1238A>T c.1402A>T (p.Ile468Phe) c.1275A>T c.1243A>T (p.Ile415Phe) c.568A>T c.1081A>T c.1377A>T c.1147A>T (p.Ile383Phe) n.2238A>T c.951A>T c.680A>T c.1147A>T c.1405A>T (p.Ile469Phe) n.1193A>T c.1001A>T | |
| 2 | g.32141912T>A | CA346502846 | SPAST | c.*1162T>A (n.*1162T>A) c.1502T>A (p.Ile501Asn) c.1499T>A (p.Ile500Asn) c.1239T>A c.1403T>A (p.Ile468Asn) c.1276T>A c.1244T>A (p.Ile415Asn) c.569T>A c.1082T>A c.1378T>A c.1148T>A (p.Ile383Asn) n.2239T>A c.952T>A c.681T>A c.1148T>A c.1406T>A (p.Ile469Asn) n.1194T>A c.1002T>A | |
| 2 | g.32141912T>C | CA44753790 | SPAST | c.*1162T>C (n.*1162T>C) c.1502T>C (p.Ile501Thr) c.1499T>C (p.Ile500Thr) c.1239T>C c.1403T>C (p.Ile468Thr) c.1276T>C c.1244T>C (p.Ile415Thr) c.569T>C c.1082T>C c.1378T>C c.1148T>C (p.Ile383Thr) n.2239T>C c.952T>C c.681T>C c.1148T>C c.1406T>C (p.Ile469Thr) n.1194T>C c.1002T>C | dbSNP |
| 2 | g.32141912T>G | CA346502849 | SPAST | c.*1162T>G (n.*1162T>G) c.1502T>G (p.Ile501Ser) c.1499T>G (p.Ile500Ser) c.1239T>G c.1403T>G (p.Ile468Ser) c.1276T>G c.1244T>G (p.Ile415Ser) c.569T>G c.1082T>G c.1378T>G c.1148T>G (p.Ile383Ser) n.2239T>G c.952T>G c.681T>G c.1148T>G c.1406T>G (p.Ile469Ser) n.1194T>G c.1002T>G | |
| 2 | g.32141912T= | CA1242504516 | SPAST | c.*1162T= (n.*1162T=) c.1502T= (p.Ile501=) c.1499T= (p.Ile500=) c.1239T= c.1403T= (p.Ile468=) c.1276T= c.1244T= (p.Ile415=) c.569T= c.1082T= c.1378T= c.1148T= (p.Ile383=) n.2239T= c.952T= c.681T= c.1148T= c.1406T= (p.Ile469=) n.1194T= c.1002T= | |
| 2 | g.32141913C>A | CA425451067 | SPAST | c.*1163C>A (n.*1163C>A) c.1503C>A (p.Ile501=) c.1500C>A (p.Ile500=) c.1240C>A c.1404C>A (p.Ile468=) c.1277C>A c.1245C>A (p.Ile415=) c.570C>A c.1083C>A c.1379C>A c.1149C>A (p.Ile383=) n.2240C>A c.953C>A c.682C>A c.1149C>A c.1407C>A (p.Ile469=) n.1195C>A c.1003C>A | gnomAD v4 |
| 2 | g.32141913C>G | CA346502850 | SPAST | c.*1163C>G (n.*1163C>G) c.1503C>G (p.Ile501Met) c.1500C>G (p.Ile500Met) c.1240C>G c.1404C>G (p.Ile468Met) c.1277C>G c.1245C>G (p.Ile415Met) c.570C>G c.1083C>G c.1379C>G c.1149C>G (p.Ile383Met) n.2240C>G c.953C>G c.682C>G c.1149C>G c.1407C>G (p.Ile469Met) n.1195C>G c.1003C>G | |
| 2 | g.32141913C>T | CA425451065 | SPAST | c.*1163C>T (n.*1163C>T) c.1503C>T (p.Ile501=) c.1500C>T (p.Ile500=) c.1240C>T c.1404C>T (p.Ile468=) c.1277C>T c.1245C>T (p.Ile415=) c.570C>T c.1083C>T c.1379C>T c.1149C>T (p.Ile383=) n.2240C>T c.953C>T c.682C>T c.1149C>T c.1407C>T (p.Ile469=) n.1195C>T c.1003C>T | |
| 2 | g.32141914A= | CA1242504517 | SPAST | c.*1164A= (n.*1164A=) c.1504A= (p.Lys502=) c.1501A= (p.Lys501=) c.1241A= c.1405A= (p.Lys469=) c.1278A= c.1246A= (p.Lys416=) c.571A= c.1084A= c.1380A= c.1150A= (p.Lys384=) n.2241A= c.954A= c.683A= c.1150A= c.1408A= (p.Lys470=) n.1196A= c.1004A= | |
| 2 | g.32141914A>C | CA346502852 | SPAST | c.*1164A>C (n.*1164A>C) c.1504A>C (p.Lys502Gln) c.1501A>C (p.Lys501Gln) c.1241A>C c.1405A>C (p.Lys469Gln) c.1278A>C c.1246A>C (p.Lys416Gln) c.571A>C c.1084A>C c.1380A>C c.1150A>C (p.Lys384Gln) n.2241A>C c.954A>C c.683A>C c.1150A>C c.1408A>C (p.Lys470Gln) n.1196A>C c.1004A>C | |
| 2 | g.32141914A>G | CA346502853 | SPAST | c.*1164A>G (n.*1164A>G) c.1504A>G (p.Lys502Glu) c.1501A>G (p.Lys501Glu) c.1241A>G c.1405A>G (p.Lys469Glu) c.1278A>G c.1246A>G (p.Lys416Glu) c.571A>G c.1084A>G c.1380A>G c.1150A>G (p.Lys384Glu) n.2241A>G c.954A>G c.683A>G c.1150A>G c.1408A>G (p.Lys470Glu) n.1196A>G c.1004A>G | ClinVar gnomAD v4 |
| 2 | g.32141914A>T | CA346502855 | SPAST | c.*1164A>T (n.*1164A>T) c.1504A>T (p.Lys502Ter) c.1501A>T (p.Lys501Ter) c.1241A>T c.1405A>T (p.Lys469Ter) c.1278A>T c.1246A>T (p.Lys416Ter) c.571A>T c.1084A>T c.1380A>T c.1150A>T (p.Lys384Ter) n.2241A>T c.954A>T c.683A>T c.1150A>T c.1408A>T (p.Lys470Ter) n.1196A>T c.1004A>T | dbSNP |
| 2 | g.32141916del | CA2499215912 | SPAST | c.*1166del (n.*1166del) c.1506del (p.Lys502AsnfsTer28) c.1503del (p.Lys501AsnfsTer28) c.1243del c.1407del (p.Lys469AsnfsTer28) c.1280del c.1248del (p.Lys416AsnfsTer28) c.573del c.1086del c.1382del c.1152del (p.Lys384AsnfsTer28) n.2243del c.956del c.685del c.1152del c.1410del (p.Lys470AsnfsTer28) n.1198del c.1006del | ClinVar dbSNP |
| 2 | g.32141915A= | CA1242504518 | SPAST | c.*1165A= (n.*1165A=) c.1505A= (p.Lys502=) c.1502A= (p.Lys501=) c.1242A= c.1406A= (p.Lys469=) c.1279A= c.1247A= (p.Lys416=) c.572A= c.1085A= c.1381A= c.1151A= (p.Lys384=) n.2242A= c.955A= c.684A= c.1151A= c.1409A= (p.Lys470=) n.1197A= c.1005A= | |
| 2 | g.32141915A>C | CA346502858 | SPAST | c.*1165A>C (n.*1165A>C) c.1505A>C (p.Lys502Thr) c.1502A>C (p.Lys501Thr) c.1242A>C c.1406A>C (p.Lys469Thr) c.1279A>C c.1247A>C (p.Lys416Thr) c.572A>C c.1085A>C c.1381A>C c.1151A>C (p.Lys384Thr) n.2242A>C c.955A>C c.684A>C c.1151A>C c.1409A>C (p.Lys470Thr) n.1197A>C c.1005A>C | ClinVar dbSNP |
| 2 | g.32141915A>G | CA346502859 | SPAST | c.*1165A>G (n.*1165A>G) c.1505A>G (p.Lys502Arg) c.1502A>G (p.Lys501Arg) c.1242A>G c.1406A>G (p.Lys469Arg) c.1279A>G c.1247A>G (p.Lys416Arg) c.572A>G c.1085A>G c.1381A>G c.1151A>G (p.Lys384Arg) n.2242A>G c.955A>G c.684A>G c.1151A>G c.1409A>G (p.Lys470Arg) n.1197A>G c.1005A>G | gnomAD v4 |
| 2 | g.32141915A>T | CA346502856 | SPAST | c.*1165A>T (n.*1165A>T) c.1505A>T (p.Lys502Ile) c.1502A>T (p.Lys501Ile) c.1242A>T c.1406A>T (p.Lys469Ile) c.1279A>T c.1247A>T (p.Lys416Ile) c.572A>T c.1085A>T c.1381A>T c.1151A>T (p.Lys384Ile) n.2242A>T c.955A>T c.684A>T c.1151A>T c.1409A>T (p.Lys470Ile) n.1197A>T c.1005A>T | |
| 2 | g.32141916A>C | CA346502863 | SPAST | c.*1166A>C (n.*1166A>C) c.1506A>C (p.Lys502Asn) c.1503A>C (p.Lys501Asn) c.1243A>C c.1407A>C (p.Lys469Asn) c.1280A>C c.1248A>C (p.Lys416Asn) c.573A>C c.1086A>C c.1382A>C c.1152A>C (p.Lys384Asn) n.2243A>C c.956A>C c.685A>C c.1152A>C c.1410A>C (p.Lys470Asn) n.1198A>C c.1006A>C | |
| 2 | g.32141916A>G | CA425451088 | SPAST | c.*1166A>G (n.*1166A>G) c.1506A>G (p.Lys502=) c.1503A>G (p.Lys501=) c.1243A>G c.1407A>G (p.Lys469=) c.1280A>G c.1248A>G (p.Lys416=) c.573A>G c.1086A>G c.1382A>G c.1152A>G (p.Lys384=) n.2243A>G c.956A>G c.685A>G c.1152A>G c.1410A>G (p.Lys470=) n.1198A>G c.1006A>G | |
| 2 | g.32141916A>T | CA346502861 | SPAST | c.*1166A>T (n.*1166A>T) c.1506A>T (p.Lys502Asn) c.1503A>T (p.Lys501Asn) c.1243A>T c.1407A>T (p.Lys469Asn) c.1280A>T c.1248A>T (p.Lys416Asn) c.573A>T c.1086A>T c.1382A>T c.1152A>T (p.Lys384Asn) n.2243A>T c.956A>T c.685A>T c.1152A>T c.1410A>T (p.Lys470Asn) n.1198A>T c.1006A>T | |
| 2 | g.32141917C>A | CA425451091 | SPAST | c.*1167C>A (n.*1167C>A) c.1507C>A (p.Arg503=) c.1504C>A (p.Arg502=) c.1244C>A c.1408C>A (p.Arg470=) c.1281C>A c.1249C>A (p.Arg417=) c.574C>A c.1087C>A c.1383C>A c.1153C>A (p.Arg385=) n.2244C>A c.957C>A c.686C>A c.1153C>A c.1411C>A (p.Arg471=) n.1199C>A c.1007C>A |