Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.38351595T>ACA490012624SPRED1c.1266T>A (p.Pro422=)
c.1302T>A (p.Pro434=)
c.1044T>A (p.Pro348=)
c.1203T>A (p.Pro401=)
15g.38351595T>CCA490012621SPRED1c.1266T>C (p.Pro422=)
c.1302T>C (p.Pro434=)
c.1044T>C (p.Pro348=)
c.1203T>C (p.Pro401=)
15g.38351595T>GCA490012623SPRED1c.1266T>G (p.Pro422=)
c.1302T>G (p.Pro434=)
c.1044T>G (p.Pro348=)
c.1203T>G (p.Pro401=)
15g.38351596T>ACA391934724SPRED1c.1267T>A (p.Leu423Met)
c.1303T>A (p.Leu435Met)
c.1045T>A (p.Leu349Met)
c.1204T>A (p.Leu402Met)
15g.38351596T>CCA490012625SPRED1c.1267T>C (p.Leu423=)
c.1303T>C (p.Leu435=)
c.1045T>C (p.Leu349=)
c.1204T>C (p.Leu402=)
 dbSNP
15g.38351596T>GCA391934725SPRED1c.1267T>G (p.Leu423Val)
c.1303T>G (p.Leu435Val)
c.1045T>G (p.Leu349Val)
c.1204T>G (p.Leu402Val)
15g.38351596T=CA2170812777SPRED1c.1267T= (p.Leu423=)
c.1303T= (p.Leu435=)
c.1045T= (p.Leu349=)
c.1204T= (p.Leu402=)
15g.38351597T>ACA391934726SPRED1c.1268T>A (p.Leu423Ter)
c.1304T>A (p.Leu435Ter)
c.1046T>A (p.Leu349Ter)
c.1205T>A (p.Leu402Ter)
15g.38351597T>CCA391934727SPRED1c.1268T>C (p.Leu423Ser)
c.1304T>C (p.Leu435Ser)
c.1046T>C (p.Leu349Ser)
c.1205T>C (p.Leu402Ser)
15g.38351597T>GCA391934728SPRED1c.1268T>G (p.Leu423Trp)
c.1304T>G (p.Leu435Trp)
c.1046T>G (p.Leu349Trp)
c.1205T>G (p.Leu402Trp)
15g.38351598G>ACA490012626SPRED1c.1269G>A (p.Leu423=)
c.1305G>A (p.Leu435=)
c.1047G>A (p.Leu349=)
c.1206G>A (p.Leu402=)
15g.38351598G>CCA391934729SPRED1c.1269G>C (p.Leu423Phe)
c.1305G>C (p.Leu435Phe)
c.1047G>C (p.Leu349Phe)
c.1206G>C (p.Leu402Phe)
 dbSNP
15g.38351598G=CA2170812778SPRED1c.1269G= (p.Leu423=)
c.1305G= (p.Leu435=)
c.1047G= (p.Leu349=)
c.1206G= (p.Leu402=)
15g.38351598G>TCA391934730SPRED1c.1269G>T (p.Leu423Phe)
c.1305G>T (p.Leu435Phe)
c.1047G>T (p.Leu349Phe)
c.1206G>T (p.Leu402Phe)
15g.38351600_38351601delCA2697554338SPRED1c.1271_1272del (p.Arg424AsnfsTer7)
c.1307_1308del (p.Arg436AsnfsTer7)
c.1049_1050del (p.Arg350AsnfsTer7)
c.1208_1209del (p.Arg403AsnfsTer7)
 ClinVar
15g.38351599A>CCA490012627SPRED1c.1270A>C (p.Arg424=)
c.1306A>C (p.Arg436=)
c.1048A>C (p.Arg350=)
c.1207A>C (p.Arg403=)
15g.38351599A>GCA391934731SPRED1c.1270A>G (p.Arg424Gly)
c.1306A>G (p.Arg436Gly)
c.1048A>G (p.Arg350Gly)
c.1207A>G (p.Arg403Gly)
15g.38351599A>TCA391934732SPRED1c.1270A>T (p.Arg424Ter)
c.1306A>T (p.Arg436Ter)
c.1048A>T (p.Arg350Ter)
c.1207A>T (p.Arg403Ter)
15g.38351600G>ACA391934733SPRED1c.1271G>A (p.Arg424Lys)
c.1307G>A (p.Arg436Lys)
c.1049G>A (p.Arg350Lys)
c.1208G>A (p.Arg403Lys)
15g.38351600G>CCA391934734SPRED1c.1271G>C (p.Arg424Thr)
c.1307G>C (p.Arg436Thr)
c.1049G>C (p.Arg350Thr)
c.1208G>C (p.Arg403Thr)
15g.38351600G>TCA391934735SPRED1c.1271G>T (p.Arg424Ile)
c.1307G>T (p.Arg436Ile)
c.1049G>T (p.Arg350Ile)
c.1208G>T (p.Arg403Ile)
15g.38351601A>CCA391934736SPRED1c.1272A>C (p.Arg424Ser)
c.1308A>C (p.Arg436Ser)
c.1050A>C (p.Arg350Ser)
c.1209A>C (p.Arg403Ser)
15g.38351601A>GCA490012633SPRED1c.1272A>G (p.Arg424=)
c.1308A>G (p.Arg436=)
c.1050A>G (p.Arg350=)
c.1209A>G (p.Arg403=)
15g.38351601A>TCA391934737SPRED1c.1272A>T (p.Arg424Ser)
c.1308A>T (p.Arg436Ser)
c.1050A>T (p.Arg350Ser)
c.1209A>T (p.Arg403Ser)
15g.38351602delCA2580089342SPRED1c.1273del (p.Met425CysfsTer?)
c.1309del (p.Met437CysfsTer?)
c.1051del (p.Met351CysfsTer?)
c.1210del (p.Met404CysfsTer?)
 ClinVar dbSNP
15g.38351602A=CA2170812779SPRED1c.1273A= (p.Met425=)
c.1309A= (p.Met437=)
c.1051A= (p.Met351=)
c.1210A= (p.Met404=)
15g.38351602A>CCA391934738SPRED1c.1273A>C (p.Met425Leu)
c.1309A>C (p.Met437Leu)
c.1051A>C (p.Met351Leu)
c.1210A>C (p.Met404Leu)
15g.38351602A>GCA7470256SPRED1c.1273A>G (p.Met425Val)
c.1309A>G (p.Met437Val)
c.1051A>G (p.Met351Val)
c.1210A>G (p.Met404Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.38351602A>TCA391934739SPRED1c.1273A>T (p.Met425Leu)
c.1309A>T (p.Met437Leu)
c.1051A>T (p.Met351Leu)
c.1210A>T (p.Met404Leu)
15g.38351602_38351603delCA2803806072SPRED1c.1273_1274del (p.Met425ValfsTer6)
c.1309_1310del (p.Met437ValfsTer6)
c.1051_1052del (p.Met351ValfsTer6)
c.1210_1211del (p.Met404ValfsTer6)
15g.38351603T>ACA391934740SPRED1c.1274T>A (p.Met425Lys)
c.1310T>A (p.Met437Lys)
c.1052T>A (p.Met351Lys)
c.1211T>A (p.Met404Lys)
15g.38351603T>CCA391934741SPRED1c.1274T>C (p.Met425Thr)
c.1310T>C (p.Met437Thr)
c.1052T>C (p.Met351Thr)
c.1211T>C (p.Met404Thr)
 gnomAD v4
15g.38351603T>GCA391934742SPRED1c.1274T>G (p.Met425Arg)
c.1310T>G (p.Met437Arg)
c.1052T>G (p.Met351Arg)
c.1211T>G (p.Met404Arg)
15g.38351604G>ACA391934743SPRED1c.1275G>A (p.Met425Ile)
c.1311G>A (p.Met437Ile)
c.1053G>A (p.Met351Ile)
c.1212G>A (p.Met404Ile)
 ClinVar
15g.38351604G>CCA391934744SPRED1c.1275G>C (p.Met425Ile)
c.1311G>C (p.Met437Ile)
c.1053G>C (p.Met351Ile)
c.1212G>C (p.Met404Ile)
15g.38351604G>TCA391934745SPRED1c.1275G>T (p.Met425Ile)
c.1311G>T (p.Met437Ile)
c.1053G>T (p.Met351Ile)
c.1212G>T (p.Met404Ile)
15g.38351604_38351605insCACA2803806073SPRED1c.1275_1276insCA (p.Cys426HisfsTer?)
c.1311_1312insCA (p.Cys438HisfsTer?)
c.1053_1054insCA (p.Cys352HisfsTer?)
c.1212_1213insCA (p.Cys405HisfsTer?)
15g.38351605T>ACA391934746SPRED1c.1276T>A (p.Cys426Ser)
c.1312T>A (p.Cys438Ser)
c.1054T>A (p.Cys352Ser)
c.1213T>A (p.Cys405Ser)
15g.38351605T>CCA391934747SPRED1c.1276T>C (p.Cys426Arg)
c.1312T>C (p.Cys438Arg)
c.1054T>C (p.Cys352Arg)
c.1213T>C (p.Cys405Arg)
15g.38351605T>GCA391934748SPRED1c.1276T>G (p.Cys426Gly)
c.1312T>G (p.Cys438Gly)
c.1054T>G (p.Cys352Gly)
c.1213T>G (p.Cys405Gly)
15g.38351606G>ACA391934750SPRED1c.1277G>A (p.Cys426Tyr)
c.1313G>A (p.Cys438Tyr)
c.1055G>A (p.Cys352Tyr)
c.1214G>A (p.Cys405Tyr)
15g.38351606G>CCA391934751SPRED1c.1277G>C (p.Cys426Ser)
c.1313G>C (p.Cys438Ser)
c.1055G>C (p.Cys352Ser)
c.1214G>C (p.Cys405Ser)
15g.38351606G>TCA391934749SPRED1c.1277G>T (p.Cys426Phe)
c.1313G>T (p.Cys438Phe)
c.1055G>T (p.Cys352Phe)
c.1214G>T (p.Cys405Phe)
15g.38351607C>ACA391934752SPRED1c.1278C>A (p.Cys426Ter)
c.1314C>A (p.Cys438Ter)
c.1056C>A (p.Cys352Ter)
c.1215C>A (p.Cys405Ter)
15g.38351607C=CA2170812780SPRED1c.1278C= (p.Cys426=)
c.1314C= (p.Cys438=)
c.1056C= (p.Cys352=)
c.1215C= (p.Cys405=)
15g.38351607C>GCA391934753SPRED1c.1278C>G (p.Cys426Trp)
c.1314C>G (p.Cys438Trp)
c.1056C>G (p.Cys352Trp)
c.1215C>G (p.Cys405Trp)
15g.38351607C>TCA490012639SPRED1c.1278C>T (p.Cys426=)
c.1314C>T (p.Cys438=)
c.1056C>T (p.Cys352=)
c.1215C>T (p.Cys405=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.38351608C>ACA391934754SPRED1c.1279C>A (p.His427Asn)
c.1315C>A (p.His439Asn)
c.1057C>A (p.His353Asn)
c.1216C>A (p.His406Asn)
 gnomAD v4
15g.38351608C>GCA391934755SPRED1c.1279C>G (p.His427Asp)
c.1315C>G (p.His439Asp)
c.1057C>G (p.His353Asp)
c.1216C>G (p.His406Asp)
15g.38351608C>TCA391934756SPRED1c.1279C>T (p.His427Tyr)
c.1315C>T (p.His439Tyr)
c.1057C>T (p.His353Tyr)
c.1216C>T (p.His406Tyr)
15g.38351609A=CA2170812781SPRED1c.1280A= (p.His427=)
c.1316A= (p.His439=)
c.1058A= (p.His353=)
c.1217A= (p.His406=)
15g.38351609A>CCA391934759SPRED1c.1280A>C (p.His427Pro)
c.1316A>C (p.His439Pro)
c.1058A>C (p.His353Pro)
c.1217A>C (p.His406Pro)
15g.38351609A>GCA391934757SPRED1c.1280A>G (p.His427Arg)
c.1316A>G (p.His439Arg)
c.1058A>G (p.His353Arg)
c.1217A>G (p.His406Arg)
 ClinVar dbSNP
15g.38351609A>TCA391934758SPRED1c.1280A>T (p.His427Leu)
c.1316A>T (p.His439Leu)
c.1058A>T (p.His353Leu)
c.1217A>T (p.His406Leu)
 gnomAD v4
15g.38351610T>ACA391934760SPRED1c.1281T>A (p.His427Gln)
c.1317T>A (p.His439Gln)
c.1059T>A (p.His353Gln)
c.1218T>A (p.His406Gln)
15g.38351610T>CCA490012645SPRED1c.1281T>C (p.His427=)
c.1317T>C (p.His439=)
c.1059T>C (p.His353=)
c.1218T>C (p.His406=)
15g.38351610T>GCA391934761SPRED1c.1281T>G (p.His427Gln)
c.1317T>G (p.His439Gln)
c.1059T>G (p.His353Gln)
c.1218T>G (p.His406Gln)
15g.38351610_38351668dupCA1139663833SPRED1c.1281_*4dup (n.1281_*4dup)
c.1317_*4dup (n.1317_*4dup)
c.1059_*4dup (n.1059_*4dup)
c.1218_*4dup (n.1218_*4dup)
 ClinVar dbSNP
15g.38351611C>ACA391934762SPRED1c.1282C>A (p.Arg428Ser)
c.1318C>A (p.Arg440Ser)
c.1060C>A (p.Arg354Ser)
c.1219C>A (p.Arg407Ser)
15g.38351611C=CA2170812782SPRED1c.1282C= (p.Arg428=)
c.1318C= (p.Arg440=)
c.1060C= (p.Arg354=)
c.1219C= (p.Arg407=)
15g.38351611C>GCA391934763SPRED1c.1282C>G (p.Arg428Gly)
c.1318C>G (p.Arg440Gly)
c.1060C>G (p.Arg354Gly)
c.1219C>G (p.Arg407Gly)
15g.38351611C>TCA16042992SPRED1c.1282C>T (p.Arg428Cys)
c.1318C>T (p.Arg440Cys)
c.1060C>T (p.Arg354Cys)
c.1219C>T (p.Arg407Cys)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.38351612G>ACA7470257SPRED1c.1283G>A (p.Arg428His)
c.1319G>A (p.Arg440His)
c.1061G>A (p.Arg354His)
c.1220G>A (p.Arg407His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
15g.38351612G>CCA391934765SPRED1c.1283G>C (p.Arg428Pro)
c.1319G>C (p.Arg440Pro)
c.1061G>C (p.Arg354Pro)
c.1220G>C (p.Arg407Pro)
15g.38351612G=CA2170812783SPRED1c.1283G= (p.Arg428=)
c.1319G= (p.Arg440=)
c.1061G= (p.Arg354=)
c.1220G= (p.Arg407=)
15g.38351612G>TCA391934764SPRED1c.1283G>T (p.Arg428Leu)
c.1319G>T (p.Arg440Leu)
c.1061G>T (p.Arg354Leu)
c.1220G>T (p.Arg407Leu)
 dbSNP gnomAD v3 gnomAD v4
15g.38351613C>ACA490012649SPRED1c.1284C>A (p.Arg428=)
c.1320C>A (p.Arg440=)
c.1062C>A (p.Arg354=)
c.1221C>A (p.Arg407=)
15g.38351613C>GCA490012650SPRED1c.1284C>G (p.Arg428=)
c.1320C>G (p.Arg440=)
c.1062C>G (p.Arg354=)
c.1221C>G (p.Arg407=)
15g.38351613C>TCA490012651SPRED1c.1284C>T (p.Arg428=)
c.1320C>T (p.Arg440=)
c.1062C>T (p.Arg354=)
c.1221C>T (p.Arg407=)
 dbSNP gnomAD v3 gnomAD v4
15g.38351614T>ACA391934766SPRED1c.1285T>A (p.Cys429Ser)
c.1321T>A (p.Cys441Ser)
c.1063T>A (p.Cys355Ser)
c.1222T>A (p.Cys408Ser)
15g.38351614T>CCA391934767SPRED1c.1285T>C (p.Cys429Arg)
c.1321T>C (p.Cys441Arg)
c.1063T>C (p.Cys355Arg)
c.1222T>C (p.Cys408Arg)
 ClinVar
15g.38351614T>GCA391934768SPRED1c.1285T>G (p.Cys429Gly)
c.1321T>G (p.Cys441Gly)
c.1063T>G (p.Cys355Gly)
c.1222T>G (p.Cys408Gly)
15g.38351615G>ACA391934769SPRED1c.1286G>A (p.Cys429Tyr)
c.1322G>A (p.Cys441Tyr)
c.1064G>A (p.Cys355Tyr)
c.1223G>A (p.Cys408Tyr)
15g.38351615G>CCA391934770SPRED1c.1286G>C (p.Cys429Ser)
c.1322G>C (p.Cys441Ser)
c.1064G>C (p.Cys355Ser)
c.1223G>C (p.Cys408Ser)
15g.38351615G>TCA391934771SPRED1c.1286G>T (p.Cys429Phe)
c.1322G>T (p.Cys441Phe)
c.1064G>T (p.Cys355Phe)
c.1223G>T (p.Cys408Phe)
15g.38351616T>ACA391934772SPRED1c.1287T>A (p.Cys429Ter)
c.1323T>A (p.Cys441Ter)
c.1065T>A (p.Cys355Ter)
c.1224T>A (p.Cys408Ter)
15g.38351616T>CCA490012656SPRED1c.1287T>C (p.Cys429=)
c.1323T>C (p.Cys441=)
c.1065T>C (p.Cys355=)
c.1224T>C (p.Cys408=)
 ClinVar
15g.38351616T>GCA391934773SPRED1c.1287T>G (p.Cys429Trp)
c.1323T>G (p.Cys441Trp)
c.1065T>G (p.Cys355Trp)
c.1224T>G (p.Cys408Trp)
15g.38351618_38351627delCA658761266SPRED1c.1289_1298del (p.Gly430ValfsTer29)
c.1325_1334del (p.Gly442ValfsTer29)
c.1067_1076del (p.Gly356ValfsTer29)
c.1226_1235del (p.Gly409ValfsTer29)
15g.38351617G>ACA391934774SPRED1c.1288G>A (p.Gly430Ser)
c.1324G>A (p.Gly442Ser)
c.1066G>A (p.Gly356Ser)
c.1225G>A (p.Gly409Ser)
15g.38351617G>CCA391934775SPRED1c.1288G>C (p.Gly430Arg)
c.1324G>C (p.Gly442Arg)
c.1066G>C (p.Gly356Arg)
c.1225G>C (p.Gly409Arg)
15g.38351617G>TCA391934776SPRED1c.1288G>T (p.Gly430Cys)
c.1324G>T (p.Gly442Cys)
c.1066G>T (p.Gly356Cys)
c.1225G>T (p.Gly409Cys)
15g.38351618G>ACA391934778SPRED1c.1289G>A (p.Gly430Asp)
c.1325G>A (p.Gly442Asp)
c.1067G>A (p.Gly356Asp)
c.1226G>A (p.Gly409Asp)
15g.38351618G>CCA7470258SPRED1c.1289G>C (p.Gly430Ala)
c.1325G>C (p.Gly442Ala)
c.1067G>C (p.Gly356Ala)
c.1226G>C (p.Gly409Ala)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.38351618G=CA2170812784SPRED1c.1289G= (p.Gly430=)
c.1325G= (p.Gly442=)
c.1067G= (p.Gly356=)
c.1226G= (p.Gly409=)
15g.38351618G>TCA391934777SPRED1c.1289G>T (p.Gly430Val)
c.1325G>T (p.Gly442Val)
c.1067G>T (p.Gly356Val)
c.1226G>T (p.Gly409Val)
15g.38351619T>ACA490012659SPRED1c.1290T>A (p.Gly430=)
c.1326T>A (p.Gly442=)
c.1068T>A (p.Gly356=)
c.1227T>A (p.Gly409=)
15g.38351619T>CCA490012660SPRED1c.1290T>C (p.Gly430=)
c.1326T>C (p.Gly442=)
c.1068T>C (p.Gly356=)
c.1227T>C (p.Gly409=)
15g.38351619T>GCA490012661SPRED1c.1290T>G (p.Gly430=)
c.1326T>G (p.Gly442=)
c.1068T>G (p.Gly356=)
c.1227T>G (p.Gly409=)
 gnomAD v4
15g.38351620G>ACA391934781SPRED1c.1291G>A (p.Glu431Lys)
c.1327G>A (p.Glu443Lys)
c.1069G>A (p.Glu357Lys)
c.1228G>A (p.Glu410Lys)
15g.38351620G>CCA391934779SPRED1c.1291G>C (p.Glu431Gln)
c.1327G>C (p.Glu443Gln)
c.1069G>C (p.Glu357Gln)
c.1228G>C (p.Glu410Gln)
15g.38351620G>TCA391934780SPRED1c.1291G>T (p.Glu431Ter)
c.1327G>T (p.Glu443Ter)
c.1069G>T (p.Glu357Ter)
c.1228G>T (p.Glu410Ter)
15g.38351621A>CCA391934782SPRED1c.1292A>C (p.Glu431Ala)
c.1328A>C (p.Glu443Ala)
c.1070A>C (p.Glu357Ala)
c.1229A>C (p.Glu410Ala)
15g.38351621A>GCA391934783SPRED1c.1292A>G (p.Glu431Gly)
c.1328A>G (p.Glu443Gly)
c.1070A>G (p.Glu357Gly)
c.1229A>G (p.Glu410Gly)
15g.38351621A>TCA391934784SPRED1c.1292A>T (p.Glu431Val)
c.1328A>T (p.Glu443Val)
c.1070A>T (p.Glu357Val)
c.1229A>T (p.Glu410Val)
15g.38351622G>ACA490012664SPRED1c.1293G>A (p.Glu431=)
c.1329G>A (p.Glu443=)
c.1071G>A (p.Glu357=)
c.1230G>A (p.Glu410=)
 gnomAD v4
15g.38351622G>CCA391934785SPRED1c.1293G>C (p.Glu431Asp)
c.1329G>C (p.Glu443Asp)
c.1071G>C (p.Glu357Asp)
c.1230G>C (p.Glu410Asp)
15g.38351622G>TCA391934786SPRED1c.1293G>T (p.Glu431Asp)
c.1329G>T (p.Glu443Asp)
c.1071G>T (p.Glu357Asp)
c.1230G>T (p.Glu410Asp)
15g.38351623G>ACA391934787SPRED1c.1294G>A (p.Ala432Thr)
c.1330G>A (p.Ala444Thr)
c.1072G>A (p.Ala358Thr)
c.1231G>A (p.Ala411Thr)
15g.38351623G>CCA391934788SPRED1c.1294G>C (p.Ala432Pro)
c.1330G>C (p.Ala444Pro)
c.1072G>C (p.Ala358Pro)
c.1231G>C (p.Ala411Pro)
15g.38351623G>TCA391934789SPRED1c.1294G>T (p.Ala432Ser)
c.1330G>T (p.Ala444Ser)
c.1072G>T (p.Ala358Ser)
c.1231G>T (p.Ala411Ser)
15g.38351624C>ACA391934790SPRED1c.1295C>A (p.Ala432Glu)
c.1331C>A (p.Ala444Glu)
c.1073C>A (p.Ala358Glu)
c.1232C>A (p.Ala411Glu)
15g.38351624C=CA2170812785SPRED1c.1295C= (p.Ala432=)
c.1331C= (p.Ala444=)
c.1073C= (p.Ala358=)
c.1232C= (p.Ala411=)
15g.38351624C>GCA391934791SPRED1c.1295C>G (p.Ala432Gly)
c.1331C>G (p.Ala444Gly)
c.1073C>G (p.Ala358Gly)
c.1232C>G (p.Ala411Gly)
15g.38351624C>TCA7470259SPRED1c.1295C>T (p.Ala432Val)
c.1331C>T (p.Ala444Val)
c.1073C>T (p.Ala358Val)
c.1232C>T (p.Ala411Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.38351625A>CCA489922951SPRED1c.1296A>C (p.Ala432=)
c.1332A>C (p.Ala444=)
c.1074A>C (p.Ala358=)
c.1233A>C (p.Ala411=)
15g.38351625A>GCA489922952SPRED1c.1296A>G (p.Ala432=)
c.1332A>G (p.Ala444=)
c.1074A>G (p.Ala358=)
c.1233A>G (p.Ala411=)
 ClinVar dbSNP gnomAD v4
15g.38351625A>TCA489922953SPRED1c.1296A>T (p.Ala432=)
c.1332A>T (p.Ala444=)
c.1074A>T (p.Ala358=)
c.1233A>T (p.Ala411=)
15g.38351626T>ACA391934794SPRED1c.1297T>A (p.Cys433Ser)
c.1333T>A (p.Cys445Ser)
c.1075T>A (p.Cys359Ser)
c.1234T>A (p.Cys412Ser)
15g.38351626T>CCA391934792SPRED1c.1297T>C (p.Cys433Arg)
c.1333T>C (p.Cys445Arg)
c.1075T>C (p.Cys359Arg)
c.1234T>C (p.Cys412Arg)
15g.38351626T>GCA391934793SPRED1c.1297T>G (p.Cys433Gly)
c.1333T>G (p.Cys445Gly)
c.1075T>G (p.Cys359Gly)
c.1234T>G (p.Cys412Gly)
15g.38351626_38351629delinsTGTGCA2170812786SPRED1c.1297_1300delinsTGTG (p.Cys433=)
c.1333_1336delinsTGTG (p.Cys445=)
c.1075_1078delinsTGTG (p.Cys359=)
c.1234_1237delinsTGTG (p.Cys412=)
15g.38351627G>ACA7470260SPRED1c.1298G>A (p.Cys433Tyr)
c.1334G>A (p.Cys445Tyr)
c.1076G>A (p.Cys359Tyr)
c.1235G>A (p.Cys412Tyr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.38351627G>CCA391934795SPRED1c.1298G>C (p.Cys433Ser)
c.1334G>C (p.Cys445Ser)
c.1076G>C (p.Cys359Ser)
c.1235G>C (p.Cys412Ser)
15g.38351627G=CA2170812787SPRED1c.1298G= (p.Cys433=)
c.1334G= (p.Cys445=)
c.1076G= (p.Cys359=)
c.1235G= (p.Cys412=)
15g.38351627G>TCA391934796SPRED1c.1298G>T (p.Cys433Phe)
c.1334G>T (p.Cys445Phe)
c.1076G>T (p.Cys359Phe)
c.1235G>T (p.Cys412Phe)
15g.38351629_38351631delCA968818059SPRED1c.1300_1302del (p.Gly434del)
c.1336_1338del (p.Gly446del)
c.1078_1080del (p.Gly360del)
c.1237_1239del (p.Gly413del)
 dbSNP gnomAD v3 gnomAD v4
15g.38351628T>ACA391934797SPRED1c.1299T>A (p.Cys433Ter)
c.1335T>A (p.Cys445Ter)
c.1077T>A (p.Cys359Ter)
c.1236T>A (p.Cys412Ter)
15g.38351628T>CCA489922954SPRED1c.1299T>C (p.Cys433=)
c.1335T>C (p.Cys445=)
c.1077T>C (p.Cys359=)
c.1236T>C (p.Cys412=)
 ClinVar dbSNP
15g.38351628T>GCA391934798SPRED1c.1299T>G (p.Cys433Trp)
c.1335T>G (p.Cys445Trp)
c.1077T>G (p.Cys359Trp)
c.1236T>G (p.Cys412Trp)
15g.38351629G>ACA391934799SPRED1c.1300G>A (p.Gly434Ser)
c.1336G>A (p.Gly446Ser)
c.1078G>A (p.Gly360Ser)
c.1237G>A (p.Gly413Ser)
 gnomAD v4
15g.38351629G>CCA391934800SPRED1c.1300G>C (p.Gly434Arg)
c.1336G>C (p.Gly446Arg)
c.1078G>C (p.Gly360Arg)
c.1237G>C (p.Gly413Arg)
15g.38351629G>TCA391934801SPRED1c.1300G>T (p.Gly434Cys)
c.1336G>T (p.Gly446Cys)
c.1078G>T (p.Gly360Cys)
c.1237G>T (p.Gly413Cys)
 ClinVar gnomAD v4
15g.38351630G>ACA391934802SPRED1c.1301G>A (p.Gly434Asp)
c.1337G>A (p.Gly446Asp)
c.1079G>A (p.Gly360Asp)
c.1238G>A (p.Gly413Asp)
 gnomAD v4
15g.38351630G>CCA391934803SPRED1c.1301G>C (p.Gly434Ala)
c.1337G>C (p.Gly446Ala)
c.1079G>C (p.Gly360Ala)
c.1238G>C (p.Gly413Ala)
15g.38351630G=CA2170812788SPRED1c.1301G= (p.Gly434=)
c.1337G= (p.Gly446=)
c.1079G= (p.Gly360=)
c.1238G= (p.Gly413=)
15g.38351630G>TCA7470261SPRED1c.1301G>T (p.Gly434Val)
c.1337G>T (p.Gly446Val)
c.1079G>T (p.Gly360Val)
c.1238G>T (p.Gly413Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.38351631T>ACA489922955SPRED1c.1302T>A (p.Gly434=)
c.1338T>A (p.Gly446=)
c.1080T>A (p.Gly360=)
c.1239T>A (p.Gly413=)
15g.38351631T>CCA489922956SPRED1c.1302T>C (p.Gly434=)
c.1338T>C (p.Gly446=)
c.1080T>C (p.Gly360=)
c.1239T>C (p.Gly413=)
15g.38351631T>GCA489922957SPRED1c.1302T>G (p.Gly434=)
c.1338T>G (p.Gly446=)
c.1080T>G (p.Gly360=)
c.1239T>G (p.Gly413=)
15g.38351632T>ACA391934806SPRED1c.1303T>A (p.Cys435Ser)
c.1339T>A (p.Cys447Ser)
c.1081T>A (p.Cys361Ser)
c.1240T>A (p.Cys414Ser)
15g.38351632T>CCA391934805SPRED1c.1303T>C (p.Cys435Arg)
c.1339T>C (p.Cys447Arg)
c.1081T>C (p.Cys361Arg)
c.1240T>C (p.Cys414Arg)
15g.38351632T>GCA391934804SPRED1c.1303T>G (p.Cys435Gly)
c.1339T>G (p.Cys447Gly)
c.1081T>G (p.Cys361Gly)
c.1240T>G (p.Cys414Gly)
15g.38351633G>ACA391934807SPRED1c.1304G>A (p.Cys435Tyr)
c.1340G>A (p.Cys447Tyr)
c.1082G>A (p.Cys361Tyr)
c.1241G>A (p.Cys414Tyr)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.38351633G>CCA391934808SPRED1c.1304G>C (p.Cys435Ser)
c.1340G>C (p.Cys447Ser)
c.1082G>C (p.Cys361Ser)
c.1241G>C (p.Cys414Ser)
15g.38351633G=CA2170812789SPRED1c.1304G= (p.Cys435=)
c.1340G= (p.Cys447=)
c.1082G= (p.Cys361=)
c.1241G= (p.Cys414=)
15g.38351633G>TCA391934809SPRED1c.1304G>T (p.Cys435Phe)
c.1340G>T (p.Cys447Phe)
c.1082G>T (p.Cys361Phe)
c.1241G>T (p.Cys414Phe)
 gnomAD v4 COSMIC
15g.38351634C>ACA391934810SPRED1c.1305C>A (p.Cys435Ter)
c.1341C>A (p.Cys447Ter)
c.1083C>A (p.Cys361Ter)
c.1242C>A (p.Cys414Ter)
15g.38351634C>GCA391934811SPRED1c.1305C>G (p.Cys435Trp)
c.1341C>G (p.Cys447Trp)
c.1083C>G (p.Cys361Trp)
c.1242C>G (p.Cys414Trp)
15g.38351634C>TCA489922958SPRED1c.1305C>T (p.Cys435=)
c.1341C>T (p.Cys447=)
c.1083C>T (p.Cys361=)
c.1242C>T (p.Cys414=)
15g.38351635T>ACA391934812SPRED1c.1306T>A (p.Cys436Ser)
c.1342T>A (p.Cys448Ser)
c.1084T>A (p.Cys362Ser)
c.1243T>A (p.Cys415Ser)
15g.38351635T>CCA391934813SPRED1c.1306T>C (p.Cys436Arg)
c.1342T>C (p.Cys448Arg)
c.1084T>C (p.Cys362Arg)
c.1243T>C (p.Cys415Arg)
15g.38351635T>GCA391934814SPRED1c.1306T>G (p.Cys436Gly)
c.1342T>G (p.Cys448Gly)
c.1084T>G (p.Cys362Gly)
c.1243T>G (p.Cys415Gly)
15g.38351636G>ACA7470262SPRED1c.1307G>A (p.Cys436Tyr)
c.1343G>A (p.Cys448Tyr)
c.1085G>A (p.Cys362Tyr)
c.1244G>A (p.Cys415Tyr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.38351636G>CCA391934815SPRED1c.1307G>C (p.Cys436Ser)
c.1343G>C (p.Cys448Ser)
c.1085G>C (p.Cys362Ser)
c.1244G>C (p.Cys415Ser)
 ClinVar
15g.38351636G=CA2170812790SPRED1c.1307G= (p.Cys436=)
c.1343G= (p.Cys448=)
c.1085G= (p.Cys362=)
c.1244G= (p.Cys415=)
15g.38351636G>TCA391934816SPRED1c.1307G>T (p.Cys436Phe)
c.1343G>T (p.Cys448Phe)
c.1085G>T (p.Cys362Phe)
c.1244G>T (p.Cys415Phe)
 gnomAD v4
15g.38351637T>ACA391934817SPRED1c.1308T>A (p.Cys436Ter)
c.1344T>A (p.Cys448Ter)
c.1086T>A (p.Cys362Ter)
c.1245T>A (p.Cys415Ter)
15g.38351637T>CCA489922959SPRED1c.1308T>C (p.Cys436=)
c.1344T>C (p.Cys448=)
c.1086T>C (p.Cys362=)
c.1245T>C (p.Cys415=)
15g.38351637T>GCA391934818SPRED1c.1308T>G (p.Cys436Trp)
c.1344T>G (p.Cys448Trp)
c.1086T>G (p.Cys362Trp)
c.1245T>G (p.Cys415Trp)
15g.38351638G>ACA391934821SPRED1c.1309G>A (p.Gly437Ser)
c.1345G>A (p.Gly449Ser)
c.1087G>A (p.Gly363Ser)
c.1246G>A (p.Gly416Ser)
15g.38351638G>CCA391934819SPRED1c.1309G>C (p.Gly437Arg)
c.1345G>C (p.Gly449Arg)
c.1087G>C (p.Gly363Arg)
c.1246G>C (p.Gly416Arg)
15g.38351638G>TCA391934820SPRED1c.1309G>T (p.Gly437Cys)
c.1345G>T (p.Gly449Cys)
c.1087G>T (p.Gly363Cys)
c.1246G>T (p.Gly416Cys)
15g.38351639G>ACA391934822SPRED1c.1310G>A (p.Gly437Asp)
c.1346G>A (p.Gly449Asp)
c.1088G>A (p.Gly363Asp)
c.1247G>A (p.Gly416Asp)
15g.38351639G>CCA391934823SPRED1c.1310G>C (p.Gly437Ala)
c.1346G>C (p.Gly449Ala)
c.1088G>C (p.Gly363Ala)
c.1247G>C (p.Gly416Ala)
15g.38351639G>TCA391934824SPRED1c.1310G>T (p.Gly437Val)
c.1346G>T (p.Gly449Val)
c.1088G>T (p.Gly363Val)
c.1247G>T (p.Gly416Val)
15g.38351640T>ACA489922960SPRED1c.1311T>A (p.Gly437=)
c.1347T>A (p.Gly449=)
c.1089T>A (p.Gly363=)
c.1248T>A (p.Gly416=)
15g.38351640T>CCA489922961SPRED1c.1311T>C (p.Gly437=)
c.1347T>C (p.Gly449=)
c.1089T>C (p.Gly363=)
c.1248T>C (p.Gly416=)
15g.38351640T>GCA489922962SPRED1c.1311T>G (p.Gly437=)
c.1347T>G (p.Gly449=)
c.1089T>G (p.Gly363=)
c.1248T>G (p.Gly416=)
15g.38351641G>ACA391934825SPRED1c.1312G>A (p.Gly438Arg)
c.1348G>A (p.Gly450Arg)
c.1090G>A (p.Gly364Arg)
c.1249G>A (p.Gly417Arg)
15g.38351641G>CCA391934826SPRED1c.1312G>C (p.Gly438Arg)
c.1348G>C (p.Gly450Arg)
c.1090G>C (p.Gly364Arg)
c.1249G>C (p.Gly417Arg)
15g.38351641G>TCA391934827SPRED1c.1312G>T (p.Gly438Trp)
c.1348G>T (p.Gly450Trp)
c.1090G>T (p.Gly364Trp)
c.1249G>T (p.Gly417Trp)
15g.38351642G>ACA391934828SPRED1c.1313G>A (p.Gly438Glu)
c.1349G>A (p.Gly450Glu)
c.1091G>A (p.Gly364Glu)
c.1250G>A (p.Gly417Glu)
 gnomAD v4
15g.38351642G>CCA391934829SPRED1c.1313G>C (p.Gly438Ala)
c.1349G>C (p.Gly450Ala)
c.1091G>C (p.Gly364Ala)
c.1250G>C (p.Gly417Ala)
15g.38351642G=CA2170812791SPRED1c.1313G= (p.Gly438=)
c.1349G= (p.Gly450=)
c.1091G= (p.Gly364=)
c.1250G= (p.Gly417=)
15g.38351642G>TCA7470263SPRED1c.1313G>T (p.Gly438Val)
c.1349G>T (p.Gly450Val)
c.1091G>T (p.Gly364Val)
c.1250G>T (p.Gly417Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.38351643G>ACA489922963SPRED1c.1314G>A (p.Gly438=)
c.1350G>A (p.Gly450=)
c.1092G>A (p.Gly364=)
c.1251G>A (p.Gly417=)
15g.38351643G>CCA489922965SPRED1c.1314G>C (p.Gly438=)
c.1350G>C (p.Gly450=)
c.1092G>C (p.Gly364=)
c.1251G>C (p.Gly417=)
15g.38351643G>TCA489922964SPRED1c.1314G>T (p.Gly438=)
c.1350G>T (p.Gly450=)
c.1092G>T (p.Gly364=)
c.1251G>T (p.Gly417=)
 gnomAD v4
15g.38351644A>CCA391934830SPRED1c.1315A>C (p.Lys439Gln)
c.1351A>C (p.Lys451Gln)
c.1093A>C (p.Lys365Gln)
c.1252A>C (p.Lys418Gln)
15g.38351644A>GCA391934831SPRED1c.1315A>G (p.Lys439Glu)
c.1351A>G (p.Lys451Glu)
c.1093A>G (p.Lys365Glu)
c.1252A>G (p.Lys418Glu)
15g.38351644A>TCA391934832SPRED1c.1315A>T (p.Lys439Ter)
c.1351A>T (p.Lys451Ter)
c.1093A>T (p.Lys365Ter)
c.1252A>T (p.Lys418Ter)
15g.38351645A>CCA391934835SPRED1c.1316A>C (p.Lys439Thr)
c.1352A>C (p.Lys451Thr)
c.1094A>C (p.Lys365Thr)
c.1253A>C (p.Lys418Thr)
15g.38351645A>GCA391934834SPRED1c.1316A>G (p.Lys439Arg)
c.1352A>G (p.Lys451Arg)
c.1094A>G (p.Lys365Arg)
c.1253A>G (p.Lys418Arg)
15g.38351645A>TCA391934833SPRED1c.1316A>T (p.Lys439Ile)
c.1352A>T (p.Lys451Ile)
c.1094A>T (p.Lys365Ile)
c.1253A>T (p.Lys418Ile)
15g.38351646A>CCA391934836SPRED1c.1317A>C (p.Lys439Asn)
c.1353A>C (p.Lys451Asn)
c.1095A>C (p.Lys365Asn)
c.1254A>C (p.Lys418Asn)
15g.38351646A>GCA489922966SPRED1c.1317A>G (p.Lys439=)
c.1353A>G (p.Lys451=)
c.1095A>G (p.Lys365=)
c.1254A>G (p.Lys418=)
 ClinVar
15g.38351646A>TCA391934837SPRED1c.1317A>T (p.Lys439Asn)
c.1353A>T (p.Lys451Asn)
c.1095A>T (p.Lys365Asn)
c.1254A>T (p.Lys418Asn)
15g.38351647C>ACA391934838SPRED1c.1318C>A (p.His440Asn)
c.1354C>A (p.His452Asn)
c.1096C>A (p.His366Asn)
c.1255C>A (p.His419Asn)
15g.38351647C>GCA391934840SPRED1c.1318C>G (p.His440Asp)
c.1354C>G (p.His452Asp)
c.1096C>G (p.His366Asp)
c.1255C>G (p.His419Asp)
15g.38351647C>TCA391934839SPRED1c.1318C>T (p.His440Tyr)
c.1354C>T (p.His452Tyr)
c.1096C>T (p.His366Tyr)
c.1255C>T (p.His419Tyr)
15g.38351647_38351649delinsCATCA2170812792SPRED1c.1318_1320delinsCAT (p.His440=)
c.1354_1356delinsCAT (p.His452=)
c.1096_1098delinsCAT (p.His366=)
c.1255_1257delinsCAT (p.His419=)
15g.38351648A>CCA391934841SPRED1c.1319A>C (p.His440Pro)
c.1355A>C (p.His452Pro)
c.1097A>C (p.His366Pro)
c.1256A>C (p.His419Pro)
15g.38351648A>GCA391934842SPRED1c.1319A>G (p.His440Arg)
c.1355A>G (p.His452Arg)
c.1097A>G (p.His366Arg)
c.1256A>G (p.His419Arg)
15g.38351648A>TCA391934843SPRED1c.1319A>T (p.His440Leu)
c.1355A>T (p.His452Leu)
c.1097A>T (p.His366Leu)
c.1256A>T (p.His419Leu)
15g.38351649_38351650delCA7470264SPRED1c.1320_1321del (p.His440GlnfsTer23)
c.1356_1357del (p.His452GlnfsTer23)
c.1098_1099del (p.His366GlnfsTer23)
c.1257_1258del (p.His419GlnfsTer23)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.38351649T>ACA391934844SPRED1c.1320T>A (p.His440Gln)
c.1356T>A (p.His452Gln)
c.1098T>A (p.His366Gln)
c.1257T>A (p.His419Gln)
15g.38351649T>CCA489922967SPRED1c.1320T>C (p.His440=)
c.1356T>C (p.His452=)
c.1098T>C (p.His366=)
c.1257T>C (p.His419=)
15g.38351649T>GCA391934845SPRED1c.1320T>G (p.His440Gln)
c.1356T>G (p.His452Gln)
c.1098T>G (p.His366Gln)
c.1257T>G (p.His419Gln)
15g.38351650A>CCA391934848SPRED1c.1321A>C (p.Lys441Gln)
c.1357A>C (p.Lys453Gln)
c.1099A>C (p.Lys367Gln)
c.1258A>C (p.Lys420Gln)
15g.38351650A>GCA391934846SPRED1c.1321A>G (p.Lys441Glu)
c.1357A>G (p.Lys453Glu)
c.1099A>G (p.Lys367Glu)
c.1258A>G (p.Lys420Glu)
15g.38351650A>TCA391934847SPRED1c.1321A>T (p.Lys441Ter)
c.1357A>T (p.Lys453Ter)
c.1099A>T (p.Lys367Ter)
c.1258A>T (p.Lys420Ter)
15g.38351651A>CCA391934849SPRED1c.1322A>C (p.Lys441Thr)
c.1358A>C (p.Lys453Thr)
c.1100A>C (p.Lys367Thr)
c.1259A>C (p.Lys420Thr)
15g.38351651A>GCA391934850SPRED1c.1322A>G (p.Lys441Arg)
c.1358A>G (p.Lys453Arg)
c.1100A>G (p.Lys367Arg)
c.1259A>G (p.Lys420Arg)
15g.38351651A>TCA391934851SPRED1c.1322A>T (p.Lys441Ile)
c.1358A>T (p.Lys453Ile)
c.1100A>T (p.Lys367Ile)
c.1259A>T (p.Lys420Ile)
15g.38351652A>CCA391934852SPRED1c.1323A>C (p.Lys441Asn)
c.1359A>C (p.Lys453Asn)
c.1101A>C (p.Lys367Asn)
c.1260A>C (p.Lys420Asn)
15g.38351652A>GCA489922968SPRED1c.1323A>G (p.Lys441=)
c.1359A>G (p.Lys453=)
c.1101A>G (p.Lys367=)
c.1260A>G (p.Lys420=)
15g.38351652A>TCA391934853SPRED1c.1323A>T (p.Lys441Asn)
c.1359A>T (p.Lys453Asn)
c.1101A>T (p.Lys367Asn)
c.1260A>T (p.Lys420Asn)
15g.38351653G>ACA7470265SPRED1c.1324G>A (p.Ala442Thr)
c.1360G>A (p.Ala454Thr)
c.1102G>A (p.Ala368Thr)
c.1261G>A (p.Ala421Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.38351653G>CCA391934854SPRED1c.1324G>C (p.Ala442Pro)
c.1360G>C (p.Ala454Pro)
c.1102G>C (p.Ala368Pro)
c.1261G>C (p.Ala421Pro)
15g.38351653G=CA2170812793SPRED1c.1324G= (p.Ala442=)
c.1360G= (p.Ala454=)
c.1102G= (p.Ala368=)
c.1261G= (p.Ala421=)
15g.38351653G>TCA391934855SPRED1c.1324G>T (p.Ala442Ser)
c.1360G>T (p.Ala454Ser)
c.1102G>T (p.Ala368Ser)
c.1261G>T (p.Ala421Ser)
15g.38351654C>ACA391934856SPRED1c.1325C>A (p.Ala442Asp)
c.1361C>A (p.Ala454Asp)
c.1103C>A (p.Ala368Asp)
c.1262C>A (p.Ala421Asp)
15g.38351654C>GCA391934857SPRED1c.1325C>G (p.Ala442Gly)
c.1361C>G (p.Ala454Gly)
c.1103C>G (p.Ala368Gly)
c.1262C>G (p.Ala421Gly)
15g.38351654C>TCA391934858SPRED1c.1325C>T (p.Ala442Val)
c.1361C>T (p.Ala454Val)
c.1103C>T (p.Ala368Val)
c.1262C>T (p.Ala421Val)
15g.38351655T>ACA489922969SPRED1c.1326T>A (p.Ala442=)
c.1362T>A (p.Ala454=)
c.1104T>A (p.Ala368=)
c.1263T>A (p.Ala421=)
15g.38351655T>CCA489922970SPRED1c.1326T>C (p.Ala442=)
c.1362T>C (p.Ala454=)
c.1104T>C (p.Ala368=)
c.1263T>C (p.Ala421=)
15g.38351655T>GCA489922971SPRED1c.1326T>G (p.Ala442=)
c.1362T>G (p.Ala454=)
c.1104T>G (p.Ala368=)
c.1263T>G (p.Ala421=)
15g.38351656G>ACA391934859SPRED1c.1327G>A (p.Ala443Thr)
c.1363G>A (p.Ala455Thr)
c.1105G>A (p.Ala369Thr)
c.1264G>A (p.Ala422Thr)
15g.38351656G>CCA391934860SPRED1c.1327G>C (p.Ala443Pro)
c.1363G>C (p.Ala455Pro)
c.1105G>C (p.Ala369Pro)
c.1264G>C (p.Ala422Pro)
 ClinVar gnomAD v4
15g.38351656G>TCA391934861SPRED1c.1327G>T (p.Ala443Ser)
c.1363G>T (p.Ala455Ser)
c.1105G>T (p.Ala369Ser)
c.1264G>T (p.Ala422Ser)
15g.38351657C>ACA391934862SPRED1c.1328C>A (p.Ala443Asp)
c.1364C>A (p.Ala455Asp)
c.1106C>A (p.Ala369Asp)
c.1265C>A (p.Ala422Asp)
15g.38351657C>GCA391934863SPRED1c.1328C>G (p.Ala443Gly)
c.1364C>G (p.Ala455Gly)
c.1106C>G (p.Ala369Gly)
c.1265C>G (p.Ala422Gly)
15g.38351657C>TCA391934864SPRED1c.1328C>T (p.Ala443Val)
c.1364C>T (p.Ala455Val)
c.1106C>T (p.Ala369Val)
c.1265C>T (p.Ala422Val)
15g.38351658T>ACA489922972SPRED1c.1329T>A (p.Ala443=)
c.1365T>A (p.Ala455=)
c.1107T>A (p.Ala369=)
c.1266T>A (p.Ala422=)
 ClinVar
15g.38351658T>CCA489922973SPRED1c.1329T>C (p.Ala443=)
c.1365T>C (p.Ala455=)
c.1107T>C (p.Ala369=)
c.1266T>C (p.Ala422=)
15g.38351658T>GCA489922974SPRED1c.1329T>G (p.Ala443=)
c.1365T>G (p.Ala455=)
c.1107T>G (p.Ala369=)
c.1266T>G (p.Ala422=)
15g.38351659G>ACA391934865SPRED1c.1330G>A (p.Gly444Arg)
c.1366G>A (p.Gly456Arg)
c.1108G>A (p.Gly370Arg)
c.1267G>A (p.Gly423Arg)
 ClinVar
15g.38351659G>CCA391934866SPRED1c.1330G>C (p.Gly444Arg)
c.1366G>C (p.Gly456Arg)
c.1108G>C (p.Gly370Arg)
c.1267G>C (p.Gly423Arg)
15g.38351659G>TCA391934867SPRED1c.1330G>T (p.Gly444Ter)
c.1366G>T (p.Gly456Ter)
c.1108G>T (p.Gly370Ter)
c.1267G>T (p.Gly423Ter)
15g.38351660G>ACA391934868SPRED1c.1331G>A (p.Gly444Glu)
c.1367G>A (p.Gly456Glu)
c.1109G>A (p.Gly370Glu)
c.1268G>A (p.Gly423Glu)
 dbSNP gnomAD v3 gnomAD v4 COSMIC
15g.38351660G>CCA391934870SPRED1c.1331G>C (p.Gly444Ala)
c.1367G>C (p.Gly456Ala)
c.1109G>C (p.Gly370Ala)
c.1268G>C (p.Gly423Ala)
 gnomAD v4
15g.38351660G=CA2170812794SPRED1c.1331G= (p.Gly444=)
c.1367G= (p.Gly456=)
c.1109G= (p.Gly370=)
c.1268G= (p.Gly423=)
15g.38351660G>TCA391934869SPRED1c.1331G>T (p.Gly444Val)
c.1367G>T (p.Gly456Val)
c.1109G>T (p.Gly370Val)
c.1268G>T (p.Gly423Val)
15g.38351661A=CA2170812795SPRED1c.1332A= (p.Gly444=)
c.1368A= (p.Gly456=)
c.1110A= (p.Gly370=)
c.1269A= (p.Gly423=)
15g.38351661A>CCA489922975SPRED1c.1332A>C (p.Gly444=)
c.1368A>C (p.Gly456=)
c.1110A>C (p.Gly370=)
c.1269A>C (p.Gly423=)
15g.38351661A>GCA489922976SPRED1c.1332A>G (p.Gly444=)
c.1368A>G (p.Gly456=)
c.1110A>G (p.Gly370=)
c.1269A>G (p.Gly423=)
 dbSNP gnomAD v2 gnomAD v4
15g.38351661A>TCA489922977SPRED1c.1332A>T (p.Gly444=)
c.1368A>T (p.Gly456=)
c.1110A>T (p.Gly370=)
c.1269A>T (p.Gly423=)
15g.38351662T>ACA391934871SPRED1c.1333T>A (p.Ter445Arg)
c.1369T>A (p.Ter457Arg)
c.1111T>A (p.Ter371Arg)
c.1270T>A (p.Ter424Arg)
15g.38351662T>CCA391934872SPRED1c.1333T>C (p.Ter445Arg)
c.1369T>C (p.Ter457Arg)
c.1111T>C (p.Ter371Arg)
c.1270T>C (p.Ter424Arg)
15g.38351662T>GCA391934873SPRED1c.1333T>G (p.Ter445Gly)
c.1369T>G (p.Ter457Gly)
c.1111T>G (p.Ter371Gly)
c.1270T>G (p.Ter424Gly)
15g.38351663G>ACA489922978SPRED1c.1334G>A (p.Ter445=)
c.1370G>A (p.Ter457=)
c.1112G>A (p.Ter371=)
c.1271G>A (p.Ter424=)
15g.38351663G>CCA391934874SPRED1c.1334G>C (p.Ter445Ser)
c.1370G>C (p.Ter457Ser)
c.1112G>C (p.Ter371Ser)
c.1271G>C (p.Ter424Ser)
15g.38351663G>TCA391934875SPRED1c.1334G>T (p.Ter445Leu)
c.1370G>T (p.Ter457Leu)
c.1112G>T (p.Ter371Leu)
c.1271G>T (p.Ter424Leu)
15g.38351664A>CCA391934876SPRED1c.1335A>C (p.Ter445Cys)
c.1371A>C (p.Ter457Cys)
c.1113A>C (p.Ter371Cys)
c.1272A>C (p.Ter424Cys)
15g.38351664A>GCA391934877SPRED1c.1335A>G (p.Ter445Trp)
c.1371A>G (p.Ter457Trp)
c.1113A>G (p.Ter371Trp)
c.1272A>G (p.Ter424Trp)
 gnomAD v4
15g.38351664A>TCA391934878SPRED1c.1335A>T (p.Ter445Cys)
c.1371A>T (p.Ter457Cys)
c.1113A>T (p.Ter371Cys)
c.1272A>T (p.Ter424Cys)
15g.38351665_38351666insTCCA2564237004SPRED1c.*1_*2insTC (n.*1_*2insTC)
15g.38351666A=CA2170812796SPRED1c.*2A= (n.*2A=)
15g.38351666A>CCA7470266SPRED1c.*2A>C (n.*2A>C)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.38351667T>GCA2575673318SPRED1c.*3T>G (n.*3T>G)
15g.38351667_38351668delCA2518566125SPRED1c.*3_*4del (n.*3_*4del)
15g.38351668G>ACA2170812798SPRED1c.*4G>A (n.*4G>A)
 dbSNP
15g.38351668G>CCA2575673319SPRED1c.*4G>C (n.*4G>C)
15g.38351668G=CA2170812797SPRED1c.*4G= (n.*4G=)
15g.38351668G>TCA2575673320SPRED1c.*4G>T (n.*4G>T)
 gnomAD v4
15g.38351669G>ACA617506035SPRED1c.*5G>A (n.*5G>A)
 dbSNP gnomAD v2 gnomAD v4
15g.38351669G=CA2170812799SPRED1c.*5G= (n.*5G=)
15g.38351669G>TCA2170812800SPRED1c.*5G>T (n.*5G>T)
 dbSNP gnomAD v4
15g.38351670T>CCA2627716214SPRED1c.*6T>C (n.*6T>C)
 gnomAD v4
15g.38351670T>GCA2627716215SPRED1c.*6T>G (n.*6T>G)
 gnomAD v4
15g.38351671C=CA2170812801SPRED1c.*7C= (n.*7C=)
15g.38351671C>TCA2170812802SPRED1c.*7C>T (n.*7C>T)
 dbSNP gnomAD v4
15g.38351672C>TCA2565543396SPRED1c.*8C>T (n.*8C>T)
 gnomAD v4
15g.38351673A=CA2170812803SPRED1c.*9A= (n.*9A=)
15g.38351673A>GCA617506037SPRED1c.*9A>G (n.*9A>G)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.38351673A>TCA2543642624SPRED1c.*9A>T (n.*9A>T)
15g.38351675_38351676delCA2803806074SPRED1c.*11_*12del (n.*11_*12del)
15g.38351675T>GCA617506038SPRED1c.*11T>G (n.*11T>G)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.38351675T=CA2170812804SPRED1c.*11T= (n.*11T=)
15g.38351676G>ACA2803806075SPRED1c.*12G>A (n.*12G>A)
15g.38351677C>ACA2575673321SPRED1c.*13C>A (n.*13C>A)
15g.38351677C=CA2170812806SPRED1c.*13C= (n.*13C=)
15g.38351677C>TCA2170812805SPRED1c.*13C>T (n.*13C>T)
 dbSNP gnomAD v4
15g.38351679A=CA2170812807SPRED1c.*15A= (n.*15A=)
15g.38351679A>GCA2170812808SPRED1c.*15A>G (n.*15A>G)
 dbSNP
15g.38351682delCA2627716216SPRED1c.*18del (n.*18del)
 gnomAD v4
15g.38351682A>CCA2515962274SPRED1c.*18A>C (n.*18A>C)
15g.38351682A>GCA2575673322SPRED1c.*18A>G (n.*18A>G)
 gnomAD v4
15g.38351683T>ACA2529705384SPRED1c.*19T>A (n.*19T>A)
15g.38351683T>CCA2627716217SPRED1c.*19T>C (n.*19T>C)
 gnomAD v4
15g.38351684G>ACA2627716218SPRED1c.*20G>A (n.*20G>A)
 gnomAD v4
15g.38351685A=CA2170812809SPRED1c.*21A= (n.*21A=)
15g.38351685A>TCA269293465SPRED1c.*21A>T (n.*21A>T)
 dbSNP
15g.38351686G>ACA2803806076SPRED1c.*22G>A (n.*22G>A)
15g.38351687C>TCA2575673323SPRED1c.*23C>T (n.*23C>T)
15g.38351689T>ACA2627716219SPRED1c.*25T>A (n.*25T>A)
 gnomAD v4
15g.38351689T>CCA2627716220SPRED1c.*25T>C (n.*25T>C)
 gnomAD v4
15g.38351689T>GCA2563600239SPRED1c.*25T>G (n.*25T>G)
15g.38351690A=CA2170812810SPRED1c.*26A= (n.*26A=)
15g.38351690A>GCA2170812811SPRED1c.*26A>G (n.*26A>G)
 dbSNP
15g.38351693dupCA2627716221SPRED1c.*29dup (n.*29dup)
 gnomAD v4
15g.38351691A>TCA2627716222SPRED1c.*27A>T (n.*27A>T)
 gnomAD v4
15g.38351693A=CA2170812812SPRED1c.*29A= (n.*29A=)
15g.38351693A>GCA617506039SPRED1c.*29A>G (n.*29A>G)
 dbSNP gnomAD v2 gnomAD v4
15g.38351694T>CCA269293466SPRED1c.*30T>C (n.*30T>C)
 dbSNP gnomAD v3 gnomAD v4
15g.38351694T=CA2170812813SPRED1c.*30T= (n.*30T=)
15g.38351695C>ACA2575673324SPRED1c.*31C>A (n.*31C>A)
15g.38351695C=CA2170812814SPRED1c.*31C= (n.*31C=)
15g.38351695C>GCA2627716223SPRED1c.*31C>G (n.*31C>G)
 gnomAD v4
15g.38351695C>TCA617506040SPRED1c.*31C>T (n.*31C>T)
 dbSNP gnomAD v2 gnomAD v4 COSMIC

Number of alleles fetched