Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.38351437C>ACA391934165SPRED1c.1108C>A (p.Leu370Ile)
c.1144C>A (p.Leu382Ile)
c.886C>A (p.Leu296Ile)
c.1045C>A (p.Leu349Ile)
15g.38351437C=CA2170812715SPRED1c.1108C= (p.Leu370=)
c.1144C= (p.Leu382=)
c.886C= (p.Leu296=)
c.1045C= (p.Leu349=)
15g.38351437C>GCA391934163SPRED1c.1108C>G (p.Leu370Val)
c.1144C>G (p.Leu382Val)
c.886C>G (p.Leu296Val)
c.1045C>G (p.Leu349Val)
15g.38351437C>TCA142268SPRED1c.1108C>T (p.Leu370Phe)
c.1144C>T (p.Leu382Phe)
c.886C>T (p.Leu296Phe)
c.1045C>T (p.Leu349Phe)
 ClinVar dbSNP
15g.38351438T>ACA391934166SPRED1c.1109T>A (p.Leu370His)
c.1145T>A (p.Leu382His)
c.887T>A (p.Leu296His)
c.1046T>A (p.Leu349His)
15g.38351438T>CCA391934170SPRED1c.1109T>C (p.Leu370Pro)
c.1145T>C (p.Leu382Pro)
c.887T>C (p.Leu296Pro)
c.1046T>C (p.Leu349Pro)
 ClinVar dbSNP
15g.38351438T>GCA391934168SPRED1c.1109T>G (p.Leu370Arg)
c.1145T>G (p.Leu382Arg)
c.887T>G (p.Leu296Arg)
c.1046T>G (p.Leu349Arg)
15g.38351439delCA645591364SPRED1c.1110del (p.Cys371ValfsTer?)
c.1146del (p.Cys383ValfsTer?)
c.888del (p.Cys297ValfsTer?)
c.1047del (p.Cys350ValfsTer?)
 COSMIC
15g.38351439C>ACA490012195SPRED1c.1110C>A (p.Leu370=)
c.1146C>A (p.Leu382=)
c.888C>A (p.Leu296=)
c.1047C>A (p.Leu349=)
15g.38351439C=CA2170812716SPRED1c.1110C= (p.Leu370=)
c.1146C= (p.Leu382=)
c.888C= (p.Leu296=)
c.1047C= (p.Leu349=)
15g.38351439C>GCA10576976SPRED1c.1110C>G (p.Leu370=)
c.1146C>G (p.Leu382=)
c.888C>G (p.Leu296=)
c.1047C>G (p.Leu349=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.38351439C>TCA490012196SPRED1c.1110C>T (p.Leu370=)
c.1146C>T (p.Leu382=)
c.888C>T (p.Leu296=)
c.1047C>T (p.Leu349=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
15g.38351440T>ACA391934173SPRED1c.1111T>A (p.Cys371Ser)
c.1147T>A (p.Cys383Ser)
c.889T>A (p.Cys297Ser)
c.1048T>A (p.Cys350Ser)
15g.38351440T>CCA391934171SPRED1c.1111T>C (p.Cys371Arg)
c.1147T>C (p.Cys383Arg)
c.889T>C (p.Cys297Arg)
c.1048T>C (p.Cys350Arg)
15g.38351440T>GCA391934172SPRED1c.1111T>G (p.Cys371Gly)
c.1147T>G (p.Cys383Gly)
c.889T>G (p.Cys297Gly)
c.1048T>G (p.Cys350Gly)
15g.38351441G>ACA391934175SPRED1c.1112G>A (p.Cys371Tyr)
c.1148G>A (p.Cys383Tyr)
c.890G>A (p.Cys297Tyr)
c.1049G>A (p.Cys350Tyr)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.38351441G>CCA391934177SPRED1c.1112G>C (p.Cys371Ser)
c.1148G>C (p.Cys383Ser)
c.890G>C (p.Cys297Ser)
c.1049G>C (p.Cys350Ser)
 ClinVar
15g.38351441G=CA2170812717SPRED1c.1112G= (p.Cys371=)
c.1148G= (p.Cys383=)
c.890G= (p.Cys297=)
c.1049G= (p.Cys350=)
15g.38351441G>TCA391934178SPRED1c.1112G>T (p.Cys371Phe)
c.1148G>T (p.Cys383Phe)
c.890G>T (p.Cys297Phe)
c.1049G>T (p.Cys350Phe)
15g.38351442T>ACA391934180SPRED1c.1113T>A (p.Cys371Ter)
c.1149T>A (p.Cys383Ter)
c.891T>A (p.Cys297Ter)
c.1050T>A (p.Cys350Ter)
15g.38351442T>CCA490012199SPRED1c.1113T>C (p.Cys371=)
c.1149T>C (p.Cys383=)
c.891T>C (p.Cys297=)
c.1050T>C (p.Cys350=)
15g.38351442T>GCA391934182SPRED1c.1113T>G (p.Cys371Trp)
c.1149T>G (p.Cys383Trp)
c.891T>G (p.Cys297Trp)
c.1050T>G (p.Cys350Trp)
15g.38351443G>ACA391934184SPRED1c.1114G>A (p.Ala372Thr)
c.1150G>A (p.Ala384Thr)
c.892G>A (p.Ala298Thr)
c.1051G>A (p.Ala351Thr)
15g.38351443G>CCA391934185SPRED1c.1114G>C (p.Ala372Pro)
c.1150G>C (p.Ala384Pro)
c.892G>C (p.Ala298Pro)
c.1051G>C (p.Ala351Pro)
15g.38351443G>TCA391934186SPRED1c.1114G>T (p.Ala372Ser)
c.1150G>T (p.Ala384Ser)
c.892G>T (p.Ala298Ser)
c.1051G>T (p.Ala351Ser)
 gnomAD v2 gnomAD v4
15g.38351444C>ACA391934188SPRED1c.1115C>A (p.Ala372Glu)
c.1151C>A (p.Ala384Glu)
c.893C>A (p.Ala298Glu)
c.1052C>A (p.Ala351Glu)
15g.38351444C>GCA391934190SPRED1c.1115C>G (p.Ala372Gly)
c.1151C>G (p.Ala384Gly)
c.893C>G (p.Ala298Gly)
c.1052C>G (p.Ala351Gly)
15g.38351444C>TCA391934192SPRED1c.1115C>T (p.Ala372Val)
c.1151C>T (p.Ala384Val)
c.893C>T (p.Ala298Val)
c.1052C>T (p.Ala351Val)
 gnomAD v4
15g.38351445A>CCA490012203SPRED1c.1116A>C (p.Ala372=)
c.1152A>C (p.Ala384=)
c.894A>C (p.Ala298=)
c.1053A>C (p.Ala351=)
15g.38351445A>GCA490012206SPRED1c.1116A>G (p.Ala372=)
c.1152A>G (p.Ala384=)
c.894A>G (p.Ala298=)
c.1053A>G (p.Ala351=)
15g.38351445A>TCA490012207SPRED1c.1116A>T (p.Ala372=)
c.1152A>T (p.Ala384=)
c.894A>T (p.Ala298=)
c.1053A>T (p.Ala351=)
15g.38351446G>ACA391934196SPRED1c.1117G>A (p.Glu373Lys)
c.1153G>A (p.Glu385Lys)
c.895G>A (p.Glu299Lys)
c.1054G>A (p.Glu352Lys)
 COSMIC
15g.38351446G>CCA391934195SPRED1c.1117G>C (p.Glu373Gln)
c.1153G>C (p.Glu385Gln)
c.895G>C (p.Glu299Gln)
c.1054G>C (p.Glu352Gln)
 ClinVar
15g.38351446G>TCA391934193SPRED1c.1117G>T (p.Glu373Ter)
c.1153G>T (p.Glu385Ter)
c.895G>T (p.Glu299Ter)
c.1054G>T (p.Glu352Ter)
 ClinVar
15g.38351447A>CCA391934198SPRED1c.1118A>C (p.Glu373Ala)
c.1154A>C (p.Glu385Ala)
c.896A>C (p.Glu299Ala)
c.1055A>C (p.Glu352Ala)
15g.38351447A>GCA391934200SPRED1c.1118A>G (p.Glu373Gly)
c.1154A>G (p.Glu385Gly)
c.896A>G (p.Glu299Gly)
c.1055A>G (p.Glu352Gly)
15g.38351447A>TCA391934201SPRED1c.1118A>T (p.Glu373Val)
c.1154A>T (p.Glu385Val)
c.896A>T (p.Glu299Val)
c.1055A>T (p.Glu352Val)
15g.38351450_38351474delCA2575673317SPRED1c.1121_1145del (p.Ser374ThrfsTer24)
c.1157_1181del (p.Ser386ThrfsTer24)
c.899_923del (p.Ser300ThrfsTer24)
c.1058_1082del (p.Ser353ThrfsTer24)
15g.38351448G>ACA490012211SPRED1c.1119G>A (p.Glu373=)
c.1155G>A (p.Glu385=)
c.897G>A (p.Glu299=)
c.1056G>A (p.Glu352=)
15g.38351448G>CCA391934203SPRED1c.1119G>C (p.Glu373Asp)
c.1155G>C (p.Glu385Asp)
c.897G>C (p.Glu299Asp)
c.1056G>C (p.Glu352Asp)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.38351448G=CA2170812718SPRED1c.1119G= (p.Glu373=)
c.1155G= (p.Glu385=)
c.897G= (p.Glu299=)
c.1056G= (p.Glu352=)
15g.38351448G>TCA391934204SPRED1c.1119G>T (p.Glu373Asp)
c.1155G>T (p.Glu385Asp)
c.897G>T (p.Glu299Asp)
c.1056G>T (p.Glu352Asp)
 ClinVar dbSNP
15g.38351449A>CCA391934206SPRED1c.1120A>C (p.Ser374Arg)
c.1156A>C (p.Ser386Arg)
c.898A>C (p.Ser300Arg)
c.1057A>C (p.Ser353Arg)
15g.38351449A>GCA391934208SPRED1c.1120A>G (p.Ser374Gly)
c.1156A>G (p.Ser386Gly)
c.898A>G (p.Ser300Gly)
c.1057A>G (p.Ser353Gly)
15g.38351449A>TCA391934209SPRED1c.1120A>T (p.Ser374Cys)
c.1156A>T (p.Ser386Cys)
c.898A>T (p.Ser300Cys)
c.1057A>T (p.Ser353Cys)
15g.38351450G>ACA391934210SPRED1c.1121G>A (p.Ser374Asn)
c.1157G>A (p.Ser386Asn)
c.899G>A (p.Ser300Asn)
c.1058G>A (p.Ser353Asn)
15g.38351450G>CCA391934212SPRED1c.1121G>C (p.Ser374Thr)
c.1157G>C (p.Ser386Thr)
c.899G>C (p.Ser300Thr)
c.1058G>C (p.Ser353Thr)
15g.38351450G>TCA391934214SPRED1c.1121G>T (p.Ser374Ile)
c.1157G>T (p.Ser386Ile)
c.899G>T (p.Ser300Ile)
c.1058G>T (p.Ser353Ile)
 gnomAD v4
15g.38351451C>ACA391934215SPRED1c.1122C>A (p.Ser374Arg)
c.1158C>A (p.Ser386Arg)
c.900C>A (p.Ser300Arg)
c.1059C>A (p.Ser353Arg)
15g.38351451C>GCA391934216SPRED1c.1122C>G (p.Ser374Arg)
c.1158C>G (p.Ser386Arg)
c.900C>G (p.Ser300Arg)
c.1059C>G (p.Ser353Arg)
15g.38351451C>TCA490012220SPRED1c.1122C>T (p.Ser374=)
c.1158C>T (p.Ser386=)
c.900C>T (p.Ser300=)
c.1059C>T (p.Ser353=)
 COSMIC
15g.38351452A=CA2170812719SPRED1c.1123A= (p.Met375=)
c.1159A= (p.Met387=)
c.901A= (p.Met301=)
c.1060A= (p.Met354=)
15g.38351452A>CCA391934220SPRED1c.1123A>C (p.Met375Leu)
c.1159A>C (p.Met387Leu)
c.901A>C (p.Met301Leu)
c.1060A>C (p.Met354Leu)
15g.38351452A>GCA391934221SPRED1c.1123A>G (p.Met375Val)
c.1159A>G (p.Met387Val)
c.901A>G (p.Met301Val)
c.1060A>G (p.Met354Val)
 dbSNP gnomAD v4
15g.38351452A>TCA391934218SPRED1c.1123A>T (p.Met375Leu)
c.1159A>T (p.Met387Leu)
c.901A>T (p.Met301Leu)
c.1060A>T (p.Met354Leu)
15g.38351453T>ACA391934223SPRED1c.1124T>A (p.Met375Lys)
c.1160T>A (p.Met387Lys)
c.902T>A (p.Met301Lys)
c.1061T>A (p.Met354Lys)
15g.38351453T>CCA391934224SPRED1c.1124T>C (p.Met375Thr)
c.1160T>C (p.Met387Thr)
c.902T>C (p.Met301Thr)
c.1061T>C (p.Met354Thr)
15g.38351453T>GCA391934226SPRED1c.1124T>G (p.Met375Arg)
c.1160T>G (p.Met387Arg)
c.902T>G (p.Met301Arg)
c.1061T>G (p.Met354Arg)
15g.38351454G>ACA391934227SPRED1c.1125G>A (p.Met375Ile)
c.1161G>A (p.Met387Ile)
c.903G>A (p.Met301Ile)
c.1062G>A (p.Met354Ile)
 ClinVar
15g.38351454G>CCA391934229SPRED1c.1125G>C (p.Met375Ile)
c.1161G>C (p.Met387Ile)
c.903G>C (p.Met301Ile)
c.1062G>C (p.Met354Ile)
15g.38351454G=CA2170812720SPRED1c.1125G= (p.Met375=)
c.1161G= (p.Met387=)
c.903G= (p.Met301=)
c.1062G= (p.Met354=)
15g.38351454G>TCA391934230SPRED1c.1125G>T (p.Met375Ile)
c.1161G>T (p.Met387Ile)
c.903G>T (p.Met301Ile)
c.1062G>T (p.Met354Ile)
 dbSNP
15g.38351455T>ACA391934232SPRED1c.1126T>A (p.Leu376Met)
c.1162T>A (p.Leu388Met)
c.904T>A (p.Leu302Met)
c.1063T>A (p.Leu355Met)
15g.38351455T>CCA490012235SPRED1c.1126T>C (p.Leu376=)
c.1162T>C (p.Leu388=)
c.904T>C (p.Leu302=)
c.1063T>C (p.Leu355=)
15g.38351455T>GCA391934234SPRED1c.1126T>G (p.Leu376Val)
c.1162T>G (p.Leu388Val)
c.904T>G (p.Leu302Val)
c.1063T>G (p.Leu355Val)
15g.38351461_38351468delCA2573150673SPRED1c.1132_1139del (p.His378ValfsTer9)
c.1168_1175del (p.His390ValfsTer9)
c.910_917del (p.His304ValfsTer9)
c.1069_1076del (p.His357ValfsTer9)
 ClinVar dbSNP
15g.38351456T>ACA391934235SPRED1c.1127T>A (p.Leu376Ter)
c.1163T>A (p.Leu388Ter)
c.905T>A (p.Leu302Ter)
c.1064T>A (p.Leu355Ter)
15g.38351456T>CCA391934237SPRED1c.1127T>C (p.Leu376Ser)
c.1163T>C (p.Leu388Ser)
c.905T>C (p.Leu302Ser)
c.1064T>C (p.Leu355Ser)
15g.38351456T>GCA391934239SPRED1c.1127T>G (p.Leu376Trp)
c.1163T>G (p.Leu388Trp)
c.905T>G (p.Leu302Trp)
c.1064T>G (p.Leu355Trp)
15g.38351457G>ACA490012239SPRED1c.1128G>A (p.Leu376=)
c.1164G>A (p.Leu388=)
c.906G>A (p.Leu302=)
c.1065G>A (p.Leu355=)
15g.38351457G>CCA391934241SPRED1c.1128G>C (p.Leu376Phe)
c.1164G>C (p.Leu388Phe)
c.906G>C (p.Leu302Phe)
c.1065G>C (p.Leu355Phe)
15g.38351457G=CA2170812721SPRED1c.1128G= (p.Leu376=)
c.1164G= (p.Leu388=)
c.906G= (p.Leu302=)
c.1065G= (p.Leu355=)
15g.38351457G>TCA7470233SPRED1c.1128G>T (p.Leu376Phe)
c.1164G>T (p.Leu388Phe)
c.906G>T (p.Leu302Phe)
c.1065G>T (p.Leu355Phe)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.38351458T>ACA391934243SPRED1c.1129T>A (p.Tyr377Asn)
c.1165T>A (p.Tyr389Asn)
c.907T>A (p.Tyr303Asn)
c.1066T>A (p.Tyr356Asn)
15g.38351458T>CCA391934247SPRED1c.1129T>C (p.Tyr377His)
c.1165T>C (p.Tyr389His)
c.907T>C (p.Tyr303His)
c.1066T>C (p.Tyr356His)
15g.38351458T>GCA391934245SPRED1c.1129T>G (p.Tyr377Asp)
c.1165T>G (p.Tyr389Asp)
c.907T>G (p.Tyr303Asp)
c.1066T>G (p.Tyr356Asp)
15g.38351459A>CCA391934249SPRED1c.1130A>C (p.Tyr377Ser)
c.1166A>C (p.Tyr389Ser)
c.908A>C (p.Tyr303Ser)
c.1067A>C (p.Tyr356Ser)
15g.38351459A>GCA391934251SPRED1c.1130A>G (p.Tyr377Cys)
c.1166A>G (p.Tyr389Cys)
c.908A>G (p.Tyr303Cys)
c.1067A>G (p.Tyr356Cys)
15g.38351459A>TCA391934252SPRED1c.1130A>T (p.Tyr377Phe)
c.1166A>T (p.Tyr389Phe)
c.908A>T (p.Tyr303Phe)
c.1067A>T (p.Tyr356Phe)
15g.38351460T>ACA391934253SPRED1c.1131T>A (p.Tyr377Ter)
c.1167T>A (p.Tyr389Ter)
c.909T>A (p.Tyr303Ter)
c.1068T>A (p.Tyr356Ter)
15g.38351460T>CCA490012252SPRED1c.1131T>C (p.Tyr377=)
c.1167T>C (p.Tyr389=)
c.909T>C (p.Tyr303=)
c.1068T>C (p.Tyr356=)
 gnomAD v4
15g.38351460T>GCA391934254SPRED1c.1131T>G (p.Tyr377Ter)
c.1167T>G (p.Tyr389Ter)
c.909T>G (p.Tyr303Ter)
c.1068T>G (p.Tyr356Ter)
15g.38351461C>ACA391934256SPRED1c.1132C>A (p.His378Asn)
c.1168C>A (p.His390Asn)
c.910C>A (p.His304Asn)
c.1069C>A (p.His357Asn)
15g.38351461C>GCA391934258SPRED1c.1132C>G (p.His378Asp)
c.1168C>G (p.His390Asp)
c.910C>G (p.His304Asp)
c.1069C>G (p.His357Asp)
15g.38351461C>TCA391934259SPRED1c.1132C>T (p.His378Tyr)
c.1168C>T (p.His390Tyr)
c.910C>T (p.His304Tyr)
c.1069C>T (p.His357Tyr)
15g.38351462A>CCA391934261SPRED1c.1133A>C (p.His378Pro)
c.1169A>C (p.His390Pro)
c.911A>C (p.His304Pro)
c.1070A>C (p.His357Pro)
15g.38351462A>GCA391934262SPRED1c.1133A>G (p.His378Arg)
c.1169A>G (p.His390Arg)
c.911A>G (p.His304Arg)
c.1070A>G (p.His357Arg)
15g.38351462A>TCA391934263SPRED1c.1133A>T (p.His378Leu)
c.1169A>T (p.His390Leu)
c.911A>T (p.His304Leu)
c.1070A>T (p.His357Leu)
15g.38351463T>ACA391934265SPRED1c.1134T>A (p.His378Gln)
c.1170T>A (p.His390Gln)
c.912T>A (p.His304Gln)
c.1071T>A (p.His357Gln)
15g.38351463T>CCA490012261SPRED1c.1134T>C (p.His378=)
c.1170T>C (p.His390=)
c.912T>C (p.His304=)
c.1071T>C (p.His357=)
 dbSNP
15g.38351463T>GCA391934266SPRED1c.1134T>G (p.His378Gln)
c.1170T>G (p.His390Gln)
c.912T>G (p.His304Gln)
c.1071T>G (p.His357Gln)
15g.38351463T=CA2170812722SPRED1c.1134T= (p.His378=)
c.1170T= (p.His390=)
c.912T= (p.His304=)
c.1071T= (p.His357=)
15g.38351464T>ACA391934268SPRED1c.1135T>A (p.Cys379Ser)
c.1171T>A (p.Cys391Ser)
c.913T>A (p.Cys305Ser)
c.1072T>A (p.Cys358Ser)
15g.38351464T>CCA391934271SPRED1c.1135T>C (p.Cys379Arg)
c.1171T>C (p.Cys391Arg)
c.913T>C (p.Cys305Arg)
c.1072T>C (p.Cys358Arg)
15g.38351464T>GCA391934270SPRED1c.1135T>G (p.Cys379Gly)
c.1171T>G (p.Cys391Gly)
c.913T>G (p.Cys305Gly)
c.1072T>G (p.Cys358Gly)
15g.38351465G>ACA391934272SPRED1c.1136G>A (p.Cys379Tyr)
c.1172G>A (p.Cys391Tyr)
c.914G>A (p.Cys305Tyr)
c.1073G>A (p.Cys358Tyr)
15g.38351465G>CCA391934274SPRED1c.1136G>C (p.Cys379Ser)
c.1172G>C (p.Cys391Ser)
c.914G>C (p.Cys305Ser)
c.1073G>C (p.Cys358Ser)
15g.38351465G>TCA391934276SPRED1c.1136G>T (p.Cys379Phe)
c.1172G>T (p.Cys391Phe)
c.914G>T (p.Cys305Phe)
c.1073G>T (p.Cys358Phe)
 gnomAD v4
15g.38351466T>ACA391934277SPRED1c.1137T>A (p.Cys379Ter)
c.1173T>A (p.Cys391Ter)
c.915T>A (p.Cys305Ter)
c.1074T>A (p.Cys358Ter)
15g.38351466T>CCA490012264SPRED1c.1137T>C (p.Cys379=)
c.1173T>C (p.Cys391=)
c.915T>C (p.Cys305=)
c.1074T>C (p.Cys358=)
15g.38351466T>GCA391934279SPRED1c.1137T>G (p.Cys379Trp)
c.1173T>G (p.Cys391Trp)
c.915T>G (p.Cys305Trp)
c.1074T>G (p.Cys358Trp)
15g.38351467A>CCA391934280SPRED1c.1138A>C (p.Met380Leu)
c.1174A>C (p.Met392Leu)
c.916A>C (p.Met306Leu)
c.1075A>C (p.Met359Leu)
15g.38351467A>GCA391934281SPRED1c.1138A>G (p.Met380Val)
c.1174A>G (p.Met392Val)
c.916A>G (p.Met306Val)
c.1075A>G (p.Met359Val)
15g.38351467A>TCA391934283SPRED1c.1138A>T (p.Met380Leu)
c.1174A>T (p.Met392Leu)
c.916A>T (p.Met306Leu)
c.1075A>T (p.Met359Leu)
15g.38351468T>ACA391934285SPRED1c.1139T>A (p.Met380Lys)
c.1175T>A (p.Met392Lys)
c.917T>A (p.Met306Lys)
c.1076T>A (p.Met359Lys)
15g.38351468T>CCA391934286SPRED1c.1139T>C (p.Met380Thr)
c.1175T>C (p.Met392Thr)
c.917T>C (p.Met306Thr)
c.1076T>C (p.Met359Thr)
15g.38351468T>GCA391934287SPRED1c.1139T>G (p.Met380Arg)
c.1175T>G (p.Met392Arg)
c.917T>G (p.Met306Arg)
c.1076T>G (p.Met359Arg)
15g.38351469G>ACA391934292SPRED1c.1140G>A (p.Met380Ile)
c.1176G>A (p.Met392Ile)
c.918G>A (p.Met306Ile)
c.1077G>A (p.Met359Ile)
 dbSNP
15g.38351469G>CCA391934290SPRED1c.1140G>C (p.Met380Ile)
c.1176G>C (p.Met392Ile)
c.918G>C (p.Met306Ile)
c.1077G>C (p.Met359Ile)
15g.38351469G=CA2170812723SPRED1c.1140G= (p.Met380=)
c.1176G= (p.Met392=)
c.918G= (p.Met306=)
c.1077G= (p.Met359=)
15g.38351469G>TCA391934289SPRED1c.1140G>T (p.Met380Ile)
c.1176G>T (p.Met392Ile)
c.918G>T (p.Met306Ile)
c.1077G>T (p.Met359Ile)
15g.38351470T>ACA391934294SPRED1c.1141T>A (p.Ser381Thr)
c.1177T>A (p.Ser393Thr)
c.919T>A (p.Ser307Thr)
c.1078T>A (p.Ser360Thr)
15g.38351470T>CCA391934295SPRED1c.1141T>C (p.Ser381Pro)
c.1177T>C (p.Ser393Pro)
c.919T>C (p.Ser307Pro)
c.1078T>C (p.Ser360Pro)
15g.38351470T>GCA391934302SPRED1c.1141T>G (p.Ser381Ala)
c.1177T>G (p.Ser393Ala)
c.919T>G (p.Ser307Ala)
c.1078T>G (p.Ser360Ala)
15g.38351471delCA2739279996SPRED1c.1142del (p.Ser381Ter)
c.1178del (p.Ser393Ter)
c.920del (p.Ser307Ter)
c.1079del (p.Ser360Ter)
 ClinVar
15g.38351471C>ACA391934304SPRED1c.1142C>A (p.Ser381Ter)
c.1178C>A (p.Ser393Ter)
c.920C>A (p.Ser307Ter)
c.1079C>A (p.Ser360Ter)
15g.38351471C>GCA391934306SPRED1c.1142C>G (p.Ser381Ter)
c.1178C>G (p.Ser393Ter)
c.920C>G (p.Ser307Ter)
c.1079C>G (p.Ser360Ter)
 ClinVar
15g.38351471C>TCA391934308SPRED1c.1142C>T (p.Ser381Leu)
c.1178C>T (p.Ser393Leu)
c.920C>T (p.Ser307Leu)
c.1079C>T (p.Ser360Leu)
15g.38351472A>CCA490012281SPRED1c.1143A>C (p.Ser381=)
c.1179A>C (p.Ser393=)
c.921A>C (p.Ser307=)
c.1080A>C (p.Ser360=)
 ClinVar gnomAD v4
15g.38351472A>GCA490012283SPRED1c.1143A>G (p.Ser381=)
c.1179A>G (p.Ser393=)
c.921A>G (p.Ser307=)
c.1080A>G (p.Ser360=)
 ClinVar
15g.38351472A>TCA490012278SPRED1c.1143A>T (p.Ser381=)
c.1179A>T (p.Ser393=)
c.921A>T (p.Ser307=)
c.1080A>T (p.Ser360=)
15g.38351473G>ACA391934310SPRED1c.1144G>A (p.Asp382Asn)
c.1180G>A (p.Asp394Asn)
c.922G>A (p.Asp308Asn)
c.1081G>A (p.Asp361Asn)
15g.38351473G>CCA391934312SPRED1c.1144G>C (p.Asp382His)
c.1180G>C (p.Asp394His)
c.922G>C (p.Asp308His)
c.1081G>C (p.Asp361His)
15g.38351473G>TCA391934313SPRED1c.1144G>T (p.Asp382Tyr)
c.1180G>T (p.Asp394Tyr)
c.922G>T (p.Asp308Tyr)
c.1081G>T (p.Asp361Tyr)
15g.38351474A>CCA391934315SPRED1c.1145A>C (p.Asp382Ala)
c.1181A>C (p.Asp394Ala)
c.923A>C (p.Asp308Ala)
c.1082A>C (p.Asp361Ala)
15g.38351474A>GCA391934316SPRED1c.1145A>G (p.Asp382Gly)
c.1181A>G (p.Asp394Gly)
c.923A>G (p.Asp308Gly)
c.1082A>G (p.Asp361Gly)
15g.38351474A>TCA391934318SPRED1c.1145A>T (p.Asp382Val)
c.1181A>T (p.Asp394Val)
c.923A>T (p.Asp308Val)
c.1082A>T (p.Asp361Val)
 ClinVar
15g.38351475C>ACA391934321SPRED1c.1146C>A (p.Asp382Glu)
c.1182C>A (p.Asp394Glu)
c.924C>A (p.Asp308Glu)
c.1083C>A (p.Asp361Glu)
15g.38351475C=CA2170812724SPRED1c.1146C= (p.Asp382=)
c.1182C= (p.Asp394=)
c.924C= (p.Asp308=)
c.1083C= (p.Asp361=)
15g.38351475C>GCA391934322SPRED1c.1146C>G (p.Asp382Glu)
c.1182C>G (p.Asp394Glu)
c.924C>G (p.Asp308Glu)
c.1083C>G (p.Asp361Glu)
15g.38351475C>TCA490012290SPRED1c.1146C>T (p.Asp382=)
c.1182C>T (p.Asp394=)
c.924C>T (p.Asp308=)
c.1083C>T (p.Asp361=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
15g.38351476T>ACA391934324SPRED1c.1147T>A (p.Ser383Thr)
c.1183T>A (p.Ser395Thr)
c.925T>A (p.Ser309Thr)
c.1084T>A (p.Ser362Thr)
15g.38351476T>CCA7470234SPRED1c.1147T>C (p.Ser383Pro)
c.1183T>C (p.Ser395Pro)
c.925T>C (p.Ser309Pro)
c.1084T>C (p.Ser362Pro)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.38351476T>GCA391934327SPRED1c.1147T>G (p.Ser383Ala)
c.1183T>G (p.Ser395Ala)
c.925T>G (p.Ser309Ala)
c.1084T>G (p.Ser362Ala)
15g.38351476T=CA2170812725SPRED1c.1147T= (p.Ser383=)
c.1183T= (p.Ser395=)
c.925T= (p.Ser309=)
c.1084T= (p.Ser362=)
15g.38351477C>ACA391934328SPRED1c.1148C>A (p.Ser383Ter)
c.1184C>A (p.Ser395Ter)
c.926C>A (p.Ser309Ter)
c.1085C>A (p.Ser362Ter)
15g.38351477C>GCA391934329SPRED1c.1148C>G (p.Ser383Ter)
c.1184C>G (p.Ser395Ter)
c.926C>G (p.Ser309Ter)
c.1085C>G (p.Ser362Ter)
15g.38351477C>TCA391934331SPRED1c.1148C>T (p.Ser383Leu)
c.1184C>T (p.Ser395Leu)
c.926C>T (p.Ser309Leu)
c.1085C>T (p.Ser362Leu)
15g.38351477_38351479delinsCAGCA2170812726SPRED1c.1148_1150delinsCAG (p.Ser383=)
c.1184_1186delinsCAG (p.Ser395=)
c.926_928delinsCAG (p.Ser309=)
c.1085_1087delinsCAG (p.Ser362=)
15g.38351477_38351481delinsCAGAGCA2170812727SPRED1c.1148_1152delinsCAGAG (p.Ser383=)
c.1184_1188delinsCAGAG (p.Ser395=)
c.926_930delinsCAGAG (p.Ser309=)
c.1085_1089delinsCAGAG (p.Ser362=)
15g.38351478A>CCA490012300SPRED1c.1149A>C (p.Ser383=)
c.1185A>C (p.Ser395=)
c.927A>C (p.Ser309=)
c.1086A>C (p.Ser362=)
 gnomAD v4
15g.38351478A>GCA490012303SPRED1c.1149A>G (p.Ser383=)
c.1185A>G (p.Ser395=)
c.927A>G (p.Ser309=)
c.1086A>G (p.Ser362=)
15g.38351478A>TCA490012306SPRED1c.1149A>T (p.Ser383=)
c.1185A>T (p.Ser395=)
c.927A>T (p.Ser309=)
c.1086A>T (p.Ser362=)
15g.38351478_38351479delinsAGCA2170812728SPRED1c.1149_1150delinsAG (p.Ser383=)
c.1185_1186delinsAG (p.Ser395=)
c.927_928delinsAG (p.Ser309=)
c.1086_1087delinsAG (p.Ser362=)
15g.38351478_38351481delCA658761255SPRED1c.1149_1152del (p.Gly385IlefsTer20)
c.1185_1188del (p.Gly397IlefsTer20)
c.927_930del (p.Gly311IlefsTer20)
c.1086_1089del (p.Gly364IlefsTer20)
 ClinVar dbSNP gnomAD v4
15g.38351480_38351481delCA10583236SPRED1c.1151_1152del (p.Glu384GlyfsTer5)
c.1187_1188del (p.Glu396GlyfsTer5)
c.929_930del (p.Glu310GlyfsTer5)
c.1088_1089del (p.Glu363GlyfsTer5)
 ClinVar dbSNP gnomAD v4
15g.38351479delCA7470235SPRED1c.1150del (p.Glu384ArgfsTer22)
c.1186del (p.Glu396ArgfsTer22)
c.928del (p.Glu310ArgfsTer22)
c.1087del (p.Glu363ArgfsTer22)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.38351479G>ACA391934334SPRED1c.1150G>A (p.Glu384Lys)
c.1186G>A (p.Glu396Lys)
c.928G>A (p.Glu310Lys)
c.1087G>A (p.Glu363Lys)
15g.38351479G>CCA391934336SPRED1c.1150G>C (p.Glu384Gln)
c.1186G>C (p.Glu396Gln)
c.928G>C (p.Glu310Gln)
c.1087G>C (p.Glu363Gln)
15g.38351479G>TCA391934337SPRED1c.1150G>T (p.Glu384Ter)
c.1186G>T (p.Glu396Ter)
c.928G>T (p.Glu310Ter)
c.1087G>T (p.Glu363Ter)
15g.38351479_38351480delinsGACA2170812729SPRED1c.1150_1151delinsGA (p.Glu384=)
c.1186_1187delinsGA (p.Glu396=)
c.928_929delinsGA (p.Glu310=)
c.1087_1088delinsGA (p.Glu363=)
15g.38351480delCA915946532SPRED1c.1151del (p.Glu384GlyfsTer22)
c.1187del (p.Glu396GlyfsTer22)
c.929del (p.Glu310GlyfsTer22)
c.1088del (p.Glu363GlyfsTer22)
 ClinVar dbSNP
15g.38351480A>CCA391934338SPRED1c.1151A>C (p.Glu384Ala)
c.1187A>C (p.Glu396Ala)
c.929A>C (p.Glu310Ala)
c.1088A>C (p.Glu363Ala)
15g.38351480A>GCA391934339SPRED1c.1151A>G (p.Glu384Gly)
c.1187A>G (p.Glu396Gly)
c.929A>G (p.Glu310Gly)
c.1088A>G (p.Glu363Gly)
15g.38351480A>TCA391934341SPRED1c.1151A>T (p.Glu384Val)
c.1187A>T (p.Glu396Val)
c.929A>T (p.Glu310Val)
c.1088A>T (p.Glu363Val)
15g.38351481G>ACA490012316SPRED1c.1152G>A (p.Glu384=)
c.1188G>A (p.Glu396=)
c.930G>A (p.Glu310=)
c.1089G>A (p.Glu363=)
15g.38351481G>CCA391934342SPRED1c.1152G>C (p.Glu384Asp)
c.1188G>C (p.Glu396Asp)
c.930G>C (p.Glu310Asp)
c.1089G>C (p.Glu363Asp)
15g.38351481G>TCA391934344SPRED1c.1152G>T (p.Glu384Asp)
c.1188G>T (p.Glu396Asp)
c.930G>T (p.Glu310Asp)
c.1089G>T (p.Glu363Asp)
15g.38351482G>ACA391934346SPRED1c.1153G>A (p.Gly385Arg)
c.1189G>A (p.Gly397Arg)
c.931G>A (p.Gly311Arg)
c.1090G>A (p.Gly364Arg)
15g.38351482G>CCA391934347SPRED1c.1153G>C (p.Gly385Arg)
c.1189G>C (p.Gly397Arg)
c.931G>C (p.Gly311Arg)
c.1090G>C (p.Gly364Arg)
15g.38351482G>TCA391934349SPRED1c.1153G>T (p.Gly385Ter)
c.1189G>T (p.Gly397Ter)
c.931G>T (p.Gly311Ter)
c.1090G>T (p.Gly364Ter)
15g.38351483G>ACA391934351SPRED1c.1154G>A (p.Gly385Glu)
c.1190G>A (p.Gly397Glu)
c.932G>A (p.Gly311Glu)
c.1091G>A (p.Gly364Glu)
15g.38351483G>CCA391934357SPRED1c.1154G>C (p.Gly385Ala)
c.1190G>C (p.Gly397Ala)
c.932G>C (p.Gly311Ala)
c.1091G>C (p.Gly364Ala)
15g.38351483G>TCA391934360SPRED1c.1154G>T (p.Gly385Val)
c.1190G>T (p.Gly397Val)
c.932G>T (p.Gly311Val)
c.1091G>T (p.Gly364Val)
15g.38351484delCA658761258SPRED1c.1155del (p.Asp386IlefsTer20)
c.1191del (p.Asp398IlefsTer20)
c.933del (p.Asp312IlefsTer20)
c.1092del (p.Asp365IlefsTer20)
15g.38351484A>CCA490012324SPRED1c.1155A>C (p.Gly385=)
c.1191A>C (p.Gly397=)
c.933A>C (p.Gly311=)
c.1092A>C (p.Gly364=)
15g.38351484A>GCA490012326SPRED1c.1155A>G (p.Gly385=)
c.1191A>G (p.Gly397=)
c.933A>G (p.Gly311=)
c.1092A>G (p.Gly364=)
15g.38351484A>TCA490012327SPRED1c.1155A>T (p.Gly385=)
c.1191A>T (p.Gly397=)
c.933A>T (p.Gly311=)
c.1092A>T (p.Gly364=)
15g.38351485G>ACA391934362SPRED1c.1156G>A (p.Asp386Asn)
c.1192G>A (p.Asp398Asn)
c.934G>A (p.Asp312Asn)
c.1093G>A (p.Asp365Asn)
15g.38351485G>CCA391934363SPRED1c.1156G>C (p.Asp386His)
c.1192G>C (p.Asp398His)
c.934G>C (p.Asp312His)
c.1093G>C (p.Asp365His)
15g.38351485G>TCA391934365SPRED1c.1156G>T (p.Asp386Tyr)
c.1192G>T (p.Asp398Tyr)
c.934G>T (p.Asp312Tyr)
c.1093G>T (p.Asp365Tyr)
15g.38351486A>CCA391934367SPRED1c.1157A>C (p.Asp386Ala)
c.1193A>C (p.Asp398Ala)
c.935A>C (p.Asp312Ala)
c.1094A>C (p.Asp365Ala)
15g.38351486A>GCA391934368SPRED1c.1157A>G (p.Asp386Gly)
c.1193A>G (p.Asp398Gly)
c.935A>G (p.Asp312Gly)
c.1094A>G (p.Asp365Gly)
15g.38351486A>TCA391934370SPRED1c.1157A>T (p.Asp386Val)
c.1193A>T (p.Asp398Val)
c.935A>T (p.Asp312Val)
c.1094A>T (p.Asp365Val)
15g.38351487T>ACA391934373SPRED1c.1158T>A (p.Asp386Glu)
c.1194T>A (p.Asp398Glu)
c.936T>A (p.Asp312Glu)
c.1095T>A (p.Asp365Glu)
15g.38351487T>CCA490012331SPRED1c.1158T>C (p.Asp386=)
c.1194T>C (p.Asp398=)
c.936T>C (p.Asp312=)
c.1095T>C (p.Asp365=)
 ClinVar dbSNP gnomAD v4
15g.38351487T>GCA391934372SPRED1c.1158T>G (p.Asp386Glu)
c.1194T>G (p.Asp398Glu)
c.936T>G (p.Asp312Glu)
c.1095T>G (p.Asp365Glu)
15g.38351488T>ACA391934374SPRED1c.1159T>A (p.Phe387Ile)
c.1195T>A (p.Phe399Ile)
c.937T>A (p.Phe313Ile)
c.1096T>A (p.Phe366Ile)
15g.38351488T>CCA391934376SPRED1c.1159T>C (p.Phe387Leu)
c.1195T>C (p.Phe399Leu)
c.937T>C (p.Phe313Leu)
c.1096T>C (p.Phe366Leu)
15g.38351488T>GCA391934375SPRED1c.1159T>G (p.Phe387Val)
c.1195T>G (p.Phe399Val)
c.937T>G (p.Phe313Val)
c.1096T>G (p.Phe366Val)
15g.38351489T>ACA391934377SPRED1c.1160T>A (p.Phe387Tyr)
c.1196T>A (p.Phe399Tyr)
c.938T>A (p.Phe313Tyr)
c.1097T>A (p.Phe366Tyr)
15g.38351489T>CCA391934381SPRED1c.1160T>C (p.Phe387Ser)
c.1196T>C (p.Phe399Ser)
c.938T>C (p.Phe313Ser)
c.1097T>C (p.Phe366Ser)
15g.38351489T>GCA391934378SPRED1c.1160T>G (p.Phe387Cys)
c.1196T>G (p.Phe399Cys)
c.938T>G (p.Phe313Cys)
c.1097T>G (p.Phe366Cys)
15g.38351490T>ACA391934382SPRED1c.1161T>A (p.Phe387Leu)
c.1197T>A (p.Phe399Leu)
c.939T>A (p.Phe313Leu)
c.1098T>A (p.Phe366Leu)
15g.38351490T>CCA490012337SPRED1c.1161T>C (p.Phe387=)
c.1197T>C (p.Phe399=)
c.939T>C (p.Phe313=)
c.1098T>C (p.Phe366=)
15g.38351490T>GCA391934384SPRED1c.1161T>G (p.Phe387Leu)
c.1197T>G (p.Phe399Leu)
c.939T>G (p.Phe313Leu)
c.1098T>G (p.Phe366Leu)
15g.38351491T>ACA391934385SPRED1c.1162T>A (p.Ser388Thr)
c.1198T>A (p.Ser400Thr)
c.940T>A (p.Ser314Thr)
c.1099T>A (p.Ser367Thr)
15g.38351491T>CCA391934386SPRED1c.1162T>C (p.Ser388Pro)
c.1198T>C (p.Ser400Pro)
c.940T>C (p.Ser314Pro)
c.1099T>C (p.Ser367Pro)
15g.38351491T>GCA391934387SPRED1c.1162T>G (p.Ser388Ala)
c.1198T>G (p.Ser400Ala)
c.940T>G (p.Ser314Ala)
c.1099T>G (p.Ser367Ala)
15g.38351492C>ACA391934389SPRED1c.1163C>A (p.Ser388Tyr)
c.1199C>A (p.Ser400Tyr)
c.941C>A (p.Ser314Tyr)
c.1100C>A (p.Ser367Tyr)
15g.38351492C=CA2170812730SPRED1c.1163C= (p.Ser388=)
c.1199C= (p.Ser400=)
c.941C= (p.Ser314=)
c.1100C= (p.Ser367=)
15g.38351492C>GCA391934390SPRED1c.1163C>G (p.Ser388Cys)
c.1199C>G (p.Ser400Cys)
c.941C>G (p.Ser314Cys)
c.1100C>G (p.Ser367Cys)
15g.38351492C>TCA391934391SPRED1c.1163C>T (p.Ser388Phe)
c.1199C>T (p.Ser400Phe)
c.941C>T (p.Ser314Phe)
c.1100C>T (p.Ser367Phe)
 ClinVar dbSNP gnomAD v4 COSMIC
15g.38351493T>ACA490012345SPRED1c.1164T>A (p.Ser388=)
c.1200T>A (p.Ser400=)
c.942T>A (p.Ser314=)
c.1101T>A (p.Ser367=)
15g.38351493T>CCA490012347SPRED1c.1164T>C (p.Ser388=)
c.1200T>C (p.Ser400=)
c.942T>C (p.Ser314=)
c.1101T>C (p.Ser367=)
15g.38351493T>GCA490012343SPRED1c.1164T>G (p.Ser388=)
c.1200T>G (p.Ser400=)
c.942T>G (p.Ser314=)
c.1101T>G (p.Ser367=)
 dbSNP gnomAD v2 gnomAD v4
15g.38351493T=CA2170812731SPRED1c.1164T= (p.Ser388=)
c.1200T= (p.Ser400=)
c.942T= (p.Ser314=)
c.1101T= (p.Ser367=)
15g.38351494G>ACA391934393SPRED1c.1165G>A (p.Asp389Asn)
c.1201G>A (p.Asp401Asn)
c.943G>A (p.Asp315Asn)
c.1102G>A (p.Asp368Asn)
15g.38351494G>CCA269293460SPRED1c.1165G>C (p.Asp389His)
c.1201G>C (p.Asp401His)
c.943G>C (p.Asp315His)
c.1102G>C (p.Asp368His)
 dbSNP gnomAD v4
15g.38351494G=CA2170812732SPRED1c.1165G= (p.Asp389=)
c.1201G= (p.Asp401=)
c.943G= (p.Asp315=)
c.1102G= (p.Asp368=)
15g.38351494G>TCA391934395SPRED1c.1165G>T (p.Asp389Tyr)
c.1201G>T (p.Asp401Tyr)
c.943G>T (p.Asp315Tyr)
c.1102G>T (p.Asp368Tyr)
 COSMIC
15g.38351495A>CCA391934397SPRED1c.1166A>C (p.Asp389Ala)
c.1202A>C (p.Asp401Ala)
c.944A>C (p.Asp315Ala)
c.1103A>C (p.Asp368Ala)
15g.38351495A>GCA391934400SPRED1c.1166A>G (p.Asp389Gly)
c.1202A>G (p.Asp401Gly)
c.944A>G (p.Asp315Gly)
c.1103A>G (p.Asp368Gly)
15g.38351495A>TCA391934399SPRED1c.1166A>T (p.Asp389Val)
c.1202A>T (p.Asp401Val)
c.944A>T (p.Asp315Val)
c.1103A>T (p.Asp368Val)
15g.38351496T>ACA391934402SPRED1c.1167T>A (p.Asp389Glu)
c.1203T>A (p.Asp401Glu)
c.945T>A (p.Asp315Glu)
c.1104T>A (p.Asp368Glu)
15g.38351496T>CCA490012353SPRED1c.1167T>C (p.Asp389=)
c.1203T>C (p.Asp401=)
c.945T>C (p.Asp315=)
c.1104T>C (p.Asp368=)
15g.38351496T>GCA391934403SPRED1c.1167T>G (p.Asp389Glu)
c.1203T>G (p.Asp401Glu)
c.945T>G (p.Asp315Glu)
c.1104T>G (p.Asp368Glu)
15g.38351497C>ACA391934404SPRED1c.1168C>A (p.Pro390Thr)
c.1204C>A (p.Pro402Thr)
c.946C>A (p.Pro316Thr)
c.1105C>A (p.Pro369Thr)
15g.38351497C>GCA391934406SPRED1c.1168C>G (p.Pro390Ala)
c.1204C>G (p.Pro402Ala)
c.946C>G (p.Pro316Ala)
c.1105C>G (p.Pro369Ala)
15g.38351497C>TCA391934408SPRED1c.1168C>T (p.Pro390Ser)
c.1204C>T (p.Pro402Ser)
c.946C>T (p.Pro316Ser)
c.1105C>T (p.Pro369Ser)
15g.38351499delCA2627716213SPRED1c.1170del (p.Cys391ValfsTer15)
c.1206del (p.Cys403ValfsTer15)
c.948del (p.Cys317ValfsTer15)
c.1107del (p.Cys370ValfsTer15)
 gnomAD v4
15g.38351498C>ACA391934410SPRED1c.1169C>A (p.Pro390His)
c.1205C>A (p.Pro402His)
c.947C>A (p.Pro316His)
c.1106C>A (p.Pro369His)
15g.38351498C>GCA391934411SPRED1c.1169C>G (p.Pro390Arg)
c.1205C>G (p.Pro402Arg)
c.947C>G (p.Pro316Arg)
c.1106C>G (p.Pro369Arg)
15g.38351498C>TCA391934413SPRED1c.1169C>T (p.Pro390Leu)
c.1205C>T (p.Pro402Leu)
c.947C>T (p.Pro316Leu)
c.1106C>T (p.Pro369Leu)
15g.38351499C>ACA490012498SPRED1c.1170C>A (p.Pro390=)
c.1206C>A (p.Pro402=)
c.948C>A (p.Pro316=)
c.1107C>A (p.Pro369=)
15g.38351499C=CA2170812733SPRED1c.1170C= (p.Pro390=)
c.1206C= (p.Pro402=)
c.948C= (p.Pro316=)
c.1107C= (p.Pro369=)
15g.38351499C>GCA490012499SPRED1c.1170C>G (p.Pro390=)
c.1206C>G (p.Pro402=)
c.948C>G (p.Pro316=)
c.1107C>G (p.Pro369=)
 ClinVar dbSNP
15g.38351499C>TCA7470236SPRED1c.1170C>T (p.Pro390=)
c.1206C>T (p.Pro402=)
c.948C>T (p.Pro316=)
c.1107C>T (p.Pro369=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.38351500T>ACA391934417SPRED1c.1171T>A (p.Cys391Ser)
c.1207T>A (p.Cys403Ser)
c.949T>A (p.Cys317Ser)
c.1108T>A (p.Cys370Ser)
15g.38351500T>CCA391934418SPRED1c.1171T>C (p.Cys391Arg)
c.1207T>C (p.Cys403Arg)
c.949T>C (p.Cys317Arg)
c.1108T>C (p.Cys370Arg)
15g.38351500T>GCA391934416SPRED1c.1171T>G (p.Cys391Gly)
c.1207T>G (p.Cys403Gly)
c.949T>G (p.Cys317Gly)
c.1108T>G (p.Cys370Gly)
15g.38351501G>ACA391934420SPRED1c.1172G>A (p.Cys391Tyr)
c.1208G>A (p.Cys403Tyr)
c.950G>A (p.Cys317Tyr)
c.1109G>A (p.Cys370Tyr)
15g.38351501G>CCA391934421SPRED1c.1172G>C (p.Cys391Ser)
c.1208G>C (p.Cys403Ser)
c.950G>C (p.Cys317Ser)
c.1109G>C (p.Cys370Ser)
 ClinVar
15g.38351501G>TCA391934422SPRED1c.1172G>T (p.Cys391Phe)
c.1208G>T (p.Cys403Phe)
c.950G>T (p.Cys317Phe)
c.1109G>T (p.Cys370Phe)
15g.38351502T>ACA391934424SPRED1c.1173T>A (p.Cys391Ter)
c.1209T>A (p.Cys403Ter)
c.951T>A (p.Cys317Ter)
c.1110T>A (p.Cys370Ter)
15g.38351502T>CCA490012500SPRED1c.1173T>C (p.Cys391=)
c.1209T>C (p.Cys403=)
c.951T>C (p.Cys317=)
c.1110T>C (p.Cys370=)
15g.38351502T>GCA391934426SPRED1c.1173T>G (p.Cys391Trp)
c.1209T>G (p.Cys403Trp)
c.951T>G (p.Cys317Trp)
c.1110T>G (p.Cys370Trp)
15g.38351503T>ACA391934427SPRED1c.1174T>A (p.Ser392Thr)
c.1210T>A (p.Ser404Thr)
c.952T>A (p.Ser318Thr)
c.1111T>A (p.Ser371Thr)
15g.38351503T>CCA391934429SPRED1c.1174T>C (p.Ser392Pro)
c.1210T>C (p.Ser404Pro)
c.952T>C (p.Ser318Pro)
c.1111T>C (p.Ser371Pro)
15g.38351503T>GCA391934431SPRED1c.1174T>G (p.Ser392Ala)
c.1210T>G (p.Ser404Ala)
c.952T>G (p.Ser318Ala)
c.1111T>G (p.Ser371Ala)
15g.38351504C>ACA391934432SPRED1c.1175C>A (p.Ser392Ter)
c.1211C>A (p.Ser404Ter)
c.953C>A (p.Ser318Ter)
c.1112C>A (p.Ser371Ter)
 ClinVar dbSNP
15g.38351504C=CA2170812734SPRED1c.1175C= (p.Ser392=)
c.1211C= (p.Ser404=)
c.953C= (p.Ser318=)
c.1112C= (p.Ser371=)
15g.38351504C>GCA391934433SPRED1c.1175C>G (p.Ser392Trp)
c.1211C>G (p.Ser404Trp)
c.953C>G (p.Ser318Trp)
c.1112C>G (p.Ser371Trp)
 dbSNP gnomAD v2 gnomAD v4
15g.38351504C>TCA391934435SPRED1c.1175C>T (p.Ser392Leu)
c.1211C>T (p.Ser404Leu)
c.953C>T (p.Ser318Leu)
c.1112C>T (p.Ser371Leu)
 ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
15g.38351505G>ACA7470237SPRED1c.1176G>A (p.Ser392=)
c.1212G>A (p.Ser404=)
c.954G>A (p.Ser318=)
c.1113G>A (p.Ser371=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.38351505G>CCA490012504SPRED1c.1176G>C (p.Ser392=)
c.1212G>C (p.Ser404=)
c.954G>C (p.Ser318=)
c.1113G>C (p.Ser371=)
 gnomAD v4
15g.38351505G=CA2170812735SPRED1c.1176G= (p.Ser392=)
c.1212G= (p.Ser404=)
c.954G= (p.Ser318=)
c.1113G= (p.Ser371=)
15g.38351505G>TCA490012505SPRED1c.1176G>T (p.Ser392=)
c.1212G>T (p.Ser404=)
c.954G>T (p.Ser318=)
c.1113G>T (p.Ser371=)
15g.38351506T>ACA391934440SPRED1c.1177T>A (p.Cys393Ser)
c.1213T>A (p.Cys405Ser)
c.955T>A (p.Cys319Ser)
c.1114T>A (p.Cys372Ser)
15g.38351506T>CCA391934438SPRED1c.1177T>C (p.Cys393Arg)
c.1213T>C (p.Cys405Arg)
c.955T>C (p.Cys319Arg)
c.1114T>C (p.Cys372Arg)
15g.38351506T>GCA391934439SPRED1c.1177T>G (p.Cys393Gly)
c.1213T>G (p.Cys405Gly)
c.955T>G (p.Cys319Gly)
c.1114T>G (p.Cys372Gly)
15g.38351507G>ACA391934442SPRED1c.1178G>A (p.Cys393Tyr)
c.1214G>A (p.Cys405Tyr)
c.956G>A (p.Cys319Tyr)
c.1115G>A (p.Cys372Tyr)
15g.38351507G>CCA391934444SPRED1c.1178G>C (p.Cys393Ser)
c.1214G>C (p.Cys405Ser)
c.956G>C (p.Cys319Ser)
c.1115G>C (p.Cys372Ser)
15g.38351507G=CA2170812736SPRED1c.1178G= (p.Cys393=)
c.1214G= (p.Cys405=)
c.956G= (p.Cys319=)
c.1115G= (p.Cys372=)
15g.38351507G>TCA391934445SPRED1c.1178G>T (p.Cys393Phe)
c.1214G>T (p.Cys405Phe)
c.956G>T (p.Cys319Phe)
c.1115G>T (p.Cys372Phe)
 dbSNP gnomAD v2
15g.38351508T>ACA391934446SPRED1c.1179T>A (p.Cys393Ter)
c.1215T>A (p.Cys405Ter)
c.957T>A (p.Cys319Ter)
c.1116T>A (p.Cys372Ter)
15g.38351508T>CCA490012509SPRED1c.1179T>C (p.Cys393=)
c.1215T>C (p.Cys405=)
c.957T>C (p.Cys319=)
c.1116T>C (p.Cys372=)
15g.38351508T>GCA391934447SPRED1c.1179T>G (p.Cys393Trp)
c.1215T>G (p.Cys405Trp)
c.957T>G (p.Cys319Trp)
c.1116T>G (p.Cys372Trp)
15g.38351509G>ACA391934450SPRED1c.1180G>A (p.Asp394Asn)
c.1216G>A (p.Asp406Asn)
c.958G>A (p.Asp320Asn)
c.1117G>A (p.Asp373Asn)
15g.38351509G>CCA391934451SPRED1c.1180G>C (p.Asp394His)
c.1216G>C (p.Asp406His)
c.958G>C (p.Asp320His)
c.1117G>C (p.Asp373His)
15g.38351509G=CA2170812737SPRED1c.1180G= (p.Asp394=)
c.1216G= (p.Asp406=)
c.958G= (p.Asp320=)
c.1117G= (p.Asp373=)
15g.38351509G>TCA269293461SPRED1c.1180G>T (p.Asp394Tyr)
c.1216G>T (p.Asp406Tyr)
c.958G>T (p.Asp320Tyr)
c.1117G>T (p.Asp373Tyr)
 dbSNP
15g.38351510A=CA2170812738SPRED1c.1181A= (p.Asp394=)
c.1217A= (p.Asp406=)
c.959A= (p.Asp320=)
c.1118A= (p.Asp373=)
15g.38351510A>CCA391934454SPRED1c.1181A>C (p.Asp394Ala)
c.1217A>C (p.Asp406Ala)
c.959A>C (p.Asp320Ala)
c.1118A>C (p.Asp373Ala)
15g.38351510A>GCA391934456SPRED1c.1181A>G (p.Asp394Gly)
c.1217A>G (p.Asp406Gly)
c.959A>G (p.Asp320Gly)
c.1118A>G (p.Asp373Gly)
 dbSNP gnomAD v3 gnomAD v4
15g.38351510A>TCA391934457SPRED1c.1181A>T (p.Asp394Val)
c.1217A>T (p.Asp406Val)
c.959A>T (p.Asp320Val)
c.1118A>T (p.Asp373Val)
15g.38351511C>ACA391934459SPRED1c.1182C>A (p.Asp394Glu)
c.1218C>A (p.Asp406Glu)
c.960C>A (p.Asp320Glu)
c.1119C>A (p.Asp373Glu)
15g.38351511C>GCA391934461SPRED1c.1182C>G (p.Asp394Glu)
c.1218C>G (p.Asp406Glu)
c.960C>G (p.Asp320Glu)
c.1119C>G (p.Asp373Glu)
15g.38351511C>TCA490012511SPRED1c.1182C>T (p.Asp394=)
c.1218C>T (p.Asp406=)
c.960C>T (p.Asp320=)
c.1119C>T (p.Asp373=)
15g.38351512A>CCA391934464SPRED1c.1183A>C (p.Thr395Pro)
c.1219A>C (p.Thr407Pro)
c.961A>C (p.Thr321Pro)
c.1120A>C (p.Thr374Pro)
 gnomAD v4
15g.38351512A>GCA391934465SPRED1c.1183A>G (p.Thr395Ala)
c.1219A>G (p.Thr407Ala)
c.961A>G (p.Thr321Ala)
c.1120A>G (p.Thr374Ala)
15g.38351512A>TCA391934463SPRED1c.1183A>T (p.Thr395Ser)
c.1219A>T (p.Thr407Ser)
c.961A>T (p.Thr321Ser)
c.1120A>T (p.Thr374Ser)
15g.38351513C>ACA391934467SPRED1c.1184C>A (p.Thr395Asn)
c.1220C>A (p.Thr407Asn)
c.962C>A (p.Thr321Asn)
c.1121C>A (p.Thr374Asn)
15g.38351513C=CA2170812739SPRED1c.1184C= (p.Thr395=)
c.1220C= (p.Thr407=)
c.962C= (p.Thr321=)
c.1121C= (p.Thr374=)
15g.38351513C>GCA269293462SPRED1c.1184C>G (p.Thr395Ser)
c.1220C>G (p.Thr407Ser)
c.962C>G (p.Thr321Ser)
c.1121C>G (p.Thr374Ser)
 dbSNP gnomAD v4
15g.38351513C>TCA391934470SPRED1c.1184C>T (p.Thr395Ile)
c.1220C>T (p.Thr407Ile)
c.962C>T (p.Thr321Ile)
c.1121C>T (p.Thr374Ile)
 dbSNP gnomAD v3 gnomAD v4
15g.38351514T>ACA490012517SPRED1c.1185T>A (p.Thr395=)
c.1221T>A (p.Thr407=)
c.963T>A (p.Thr321=)
c.1122T>A (p.Thr374=)
15g.38351514T>CCA490012516SPRED1c.1185T>C (p.Thr395=)
c.1221T>C (p.Thr407=)
c.963T>C (p.Thr321=)
c.1122T>C (p.Thr374=)
 ClinVar gnomAD v4
15g.38351514T>GCA490012515SPRED1c.1185T>G (p.Thr395=)
c.1221T>G (p.Thr407=)
c.963T>G (p.Thr321=)
c.1122T>G (p.Thr374=)
 ClinVar dbSNP
15g.38351514T=CA2170812740SPRED1c.1185T= (p.Thr395=)
c.1221T= (p.Thr407=)
c.963T= (p.Thr321=)
c.1122T= (p.Thr374=)
15g.38351515A=CA2170812741SPRED1c.1186A= (p.Ser396=)
c.1222A= (p.Ser408=)
c.964A= (p.Ser322=)
c.1123A= (p.Ser375=)
15g.38351515A>CCA391934471SPRED1c.1186A>C (p.Ser396Arg)
c.1222A>C (p.Ser408Arg)
c.964A>C (p.Ser322Arg)
c.1123A>C (p.Ser375Arg)
15g.38351515A>GCA7470238SPRED1c.1186A>G (p.Ser396Gly)
c.1222A>G (p.Ser408Gly)
c.964A>G (p.Ser322Gly)
c.1123A>G (p.Ser375Gly)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.38351515A>TCA391934473SPRED1c.1186A>T (p.Ser396Cys)
c.1222A>T (p.Ser408Cys)
c.964A>T (p.Ser322Cys)
c.1123A>T (p.Ser375Cys)
15g.38351516G>ACA391934477SPRED1c.1187G>A (p.Ser396Asn)
c.1223G>A (p.Ser408Asn)
c.965G>A (p.Ser322Asn)
c.1124G>A (p.Ser375Asn)
15g.38351516G>CCA391934474SPRED1c.1187G>C (p.Ser396Thr)
c.1223G>C (p.Ser408Thr)
c.965G>C (p.Ser322Thr)
c.1124G>C (p.Ser375Thr)
15g.38351516G>TCA391934475SPRED1c.1187G>T (p.Ser396Ile)
c.1223G>T (p.Ser408Ile)
c.965G>T (p.Ser322Ile)
c.1124G>T (p.Ser375Ile)
15g.38351516_38351519delinsGCGACA2170812742SPRED1c.1187_1190delinsGCGA (p.Ser396=)
c.1223_1226delinsGCGA (p.Ser408=)
c.965_968delinsGCGA (p.Ser322=)
c.1124_1127delinsGCGA (p.Ser375=)
15g.38351517C>ACA391934478SPRED1c.1188C>A (p.Ser396Arg)
c.1224C>A (p.Ser408Arg)
c.966C>A (p.Ser322Arg)
c.1125C>A (p.Ser375Arg)
15g.38351517C=CA2170812743SPRED1c.1188C= (p.Ser396=)
c.1224C= (p.Ser408=)
c.966C= (p.Ser322=)
c.1125C= (p.Ser375=)
15g.38351517C>GCA391934480SPRED1c.1188C>G (p.Ser396Arg)
c.1224C>G (p.Ser408Arg)
c.966C>G (p.Ser322Arg)
c.1125C>G (p.Ser375Arg)
 dbSNP gnomAD v2 gnomAD v4
15g.38351517C>TCA7470239SPRED1c.1188C>T (p.Ser396=)
c.1224C>T (p.Ser408=)
c.966C>T (p.Ser322=)
c.1125C>T (p.Ser375=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
15g.38351521_38351523delCA645591365SPRED1c.1192_1194del (p.Asp398del)
c.1228_1230del (p.Asp410del)
c.970_972del (p.Asp324del)
c.1129_1131del (p.Asp377del)
 dbSNP gnomAD v4 COSMIC
15g.38351518G>ACA391934482SPRED1c.1189G>A (p.Asp397Asn)
c.1225G>A (p.Asp409Asn)
c.967G>A (p.Asp323Asn)
c.1126G>A (p.Asp376Asn)
 ClinVar dbSNP gnomAD v4
15g.38351518G>CCA391934483SPRED1c.1189G>C (p.Asp397His)
c.1225G>C (p.Asp409His)
c.967G>C (p.Asp323His)
c.1126G>C (p.Asp376His)
15g.38351518G=CA2170812744SPRED1c.1189G= (p.Asp397=)
c.1225G= (p.Asp409=)
c.967G= (p.Asp323=)
c.1126G= (p.Asp376=)
15g.38351518G>TCA391934486SPRED1c.1189G>T (p.Asp397Tyr)
c.1225G>T (p.Asp409Tyr)
c.967G>T (p.Asp323Tyr)
c.1126G>T (p.Asp376Tyr)
15g.38351519A>CCA391934487SPRED1c.1190A>C (p.Asp397Ala)
c.1226A>C (p.Asp409Ala)
c.968A>C (p.Asp323Ala)
c.1127A>C (p.Asp376Ala)
15g.38351519A>GCA391934489SPRED1c.1190A>G (p.Asp397Gly)
c.1226A>G (p.Asp409Gly)
c.968A>G (p.Asp323Gly)
c.1127A>G (p.Asp376Gly)
 ClinVar
15g.38351519A>TCA391934488SPRED1c.1190A>T (p.Asp397Val)
c.1226A>T (p.Asp409Val)
c.968A>T (p.Asp323Val)
c.1127A>T (p.Asp376Val)
 gnomAD v4
15g.38351520C>ACA391934490SPRED1c.1191C>A (p.Asp397Glu)
c.1227C>A (p.Asp409Glu)
c.969C>A (p.Asp323Glu)
c.1128C>A (p.Asp376Glu)
15g.38351520C=CA2170812745SPRED1c.1191C= (p.Asp397=)
c.1227C= (p.Asp409=)
c.969C= (p.Asp323=)
c.1128C= (p.Asp376=)
15g.38351520C>GCA391934491SPRED1c.1191C>G (p.Asp397Glu)
c.1227C>G (p.Asp409Glu)
c.969C>G (p.Asp323Glu)
c.1128C>G (p.Asp376Glu)
15g.38351520C>TCA7470240SPRED1c.1191C>T (p.Asp397=)
c.1227C>T (p.Asp409=)
c.969C>T (p.Asp323=)
c.1128C>T (p.Asp376=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.38351521G>ACA7470241SPRED1c.1192G>A (p.Asp398Asn)
c.1228G>A (p.Asp410Asn)
c.970G>A (p.Asp324Asn)
c.1129G>A (p.Asp377Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.38351521G>CCA391934494SPRED1c.1192G>C (p.Asp398His)
c.1228G>C (p.Asp410His)
c.970G>C (p.Asp324His)
c.1129G>C (p.Asp377His)
15g.38351521G=CA2170812746SPRED1c.1192G= (p.Asp398=)
c.1228G= (p.Asp410=)
c.970G= (p.Asp324=)
c.1129G= (p.Asp377=)
15g.38351521G>TCA391934495SPRED1c.1192G>T (p.Asp398Tyr)
c.1228G>T (p.Asp410Tyr)
c.970G>T (p.Asp324Tyr)
c.1129G>T (p.Asp377Tyr)
 ClinVar
15g.38351522A=CA2170812748SPRED1c.1193A= (p.Asp398=)
c.1229A= (p.Asp410=)
c.971A= (p.Asp324=)
c.1130A= (p.Asp377=)
15g.38351522A>CCA391934498SPRED1c.1193A>C (p.Asp398Ala)
c.1229A>C (p.Asp410Ala)
c.971A>C (p.Asp324Ala)
c.1130A>C (p.Asp377Ala)
15g.38351522A>GCA391934499SPRED1c.1193A>G (p.Asp398Gly)
c.1229A>G (p.Asp410Gly)
c.971A>G (p.Asp324Gly)
c.1130A>G (p.Asp377Gly)
15g.38351522A>TCA391934500SPRED1c.1193A>T (p.Asp398Val)
c.1229A>T (p.Asp410Val)
c.971A>T (p.Asp324Val)
c.1130A>T (p.Asp377Val)
15g.38351522_38351523delinsACCA2170812747SPRED1c.1193_1194delinsAC (p.Asp398=)
c.1229_1230delinsAC (p.Asp410=)
c.971_972delinsAC (p.Asp324=)
c.1130_1131delinsAC (p.Asp377=)
15g.38351523delCA7470242SPRED1c.1194del (p.Asp398GlufsTer8)
c.1230del (p.Asp410GlufsTer8)
c.972del (p.Asp324GlufsTer8)
c.1131del (p.Asp377GlufsTer8)
 dbSNP ExAC gnomAD v2
15g.38351523C>ACA391934501SPRED1c.1194C>A (p.Asp398Glu)
c.1230C>A (p.Asp410Glu)
c.972C>A (p.Asp324Glu)
c.1131C>A (p.Asp377Glu)
 gnomAD v4
15g.38351523C=CA2170812749SPRED1c.1194C= (p.Asp398=)
c.1230C= (p.Asp410=)
c.972C= (p.Asp324=)
c.1131C= (p.Asp377=)
15g.38351523C>GCA391934502SPRED1c.1194C>G (p.Asp398Glu)
c.1230C>G (p.Asp410Glu)
c.972C>G (p.Asp324Glu)
c.1131C>G (p.Asp377Glu)
15g.38351523C>TCA490012527SPRED1c.1194C>T (p.Asp398=)
c.1230C>T (p.Asp410=)
c.972C>T (p.Asp324=)
c.1131C>T (p.Asp377=)
 ClinVar dbSNP
15g.38351523dupCA2170812750SPRED1c.1194dup (p.Lys399GlnfsTer?)
c.1230dup (p.Lys411GlnfsTer?)
c.972dup (p.Lys325GlnfsTer?)
c.1131dup (p.Lys378GlnfsTer?)
 dbSNP
15g.38351524A>CCA391934504SPRED1c.1195A>C (p.Lys399Gln)
c.1231A>C (p.Lys411Gln)
c.973A>C (p.Lys325Gln)
c.1132A>C (p.Lys378Gln)
15g.38351524A>GCA391934506SPRED1c.1195A>G (p.Lys399Glu)
c.1231A>G (p.Lys411Glu)
c.973A>G (p.Lys325Glu)
c.1132A>G (p.Lys378Glu)
15g.38351524A>TCA391934505SPRED1c.1195A>T (p.Lys399Ter)
c.1231A>T (p.Lys411Ter)
c.973A>T (p.Lys325Ter)
c.1132A>T (p.Lys378Ter)
15g.38351525dupCA658658279SPRED1c.1196dup (p.Phe400ValfsTer?)
c.1232dup (p.Phe412ValfsTer?)
c.974dup (p.Phe326ValfsTer?)
c.1133dup (p.Phe379ValfsTer?)
 ClinVar dbSNP
15g.38351524_38351525insCTGATGCA2803806071SPRED1c.1195_1196insCTGATG (p.Lys399delinsThrAspGlu)
c.1231_1232insCTGATG (p.Lys411delinsThrAspGlu)
c.973_974insCTGATG (p.Lys325delinsThrAspGlu)
c.1132_1133insCTGATG (p.Lys378delinsThrAspGlu)
15g.38351525A>CCA391934509SPRED1c.1196A>C (p.Lys399Thr)
c.1232A>C (p.Lys411Thr)
c.974A>C (p.Lys325Thr)
c.1133A>C (p.Lys378Thr)
15g.38351525A>GCA391934510SPRED1c.1196A>G (p.Lys399Arg)
c.1232A>G (p.Lys411Arg)
c.974A>G (p.Lys325Arg)
c.1133A>G (p.Lys378Arg)
15g.38351525A>TCA391934512SPRED1c.1196A>T (p.Lys399Met)
c.1232A>T (p.Lys411Met)
c.974A>T (p.Lys325Met)
c.1133A>T (p.Lys378Met)
15g.38351526G>ACA490012533SPRED1c.1197G>A (p.Lys399=)
c.1233G>A (p.Lys411=)
c.975G>A (p.Lys325=)
c.1134G>A (p.Lys378=)
15g.38351526G>CCA391934514SPRED1c.1197G>C (p.Lys399Asn)
c.1233G>C (p.Lys411Asn)
c.975G>C (p.Lys325Asn)
c.1134G>C (p.Lys378Asn)
15g.38351526G>TCA391934516SPRED1c.1197G>T (p.Lys399Asn)
c.1233G>T (p.Lys411Asn)
c.975G>T (p.Lys325Asn)
c.1134G>T (p.Lys378Asn)
15g.38351527T>ACA391934518SPRED1c.1198T>A (p.Phe400Ile)
c.1234T>A (p.Phe412Ile)
c.976T>A (p.Phe326Ile)
c.1135T>A (p.Phe379Ile)
15g.38351527T>CCA391934519SPRED1c.1198T>C (p.Phe400Leu)
c.1234T>C (p.Phe412Leu)
c.976T>C (p.Phe326Leu)
c.1135T>C (p.Phe379Leu)
15g.38351527T>GCA391934521SPRED1c.1198T>G (p.Phe400Val)
c.1234T>G (p.Phe412Val)
c.976T>G (p.Phe326Val)
c.1135T>G (p.Phe379Val)
15g.38351528T>ACA391934523SPRED1c.1199T>A (p.Phe400Tyr)
c.1235T>A (p.Phe412Tyr)
c.977T>A (p.Phe326Tyr)
c.1136T>A (p.Phe379Tyr)
 ClinVar
15g.38351528T>CCA391934525SPRED1c.1199T>C (p.Phe400Ser)
c.1235T>C (p.Phe412Ser)
c.977T>C (p.Phe326Ser)
c.1136T>C (p.Phe379Ser)
 gnomAD v4
15g.38351528T>GCA391934527SPRED1c.1199T>G (p.Phe400Cys)
c.1235T>G (p.Phe412Cys)
c.977T>G (p.Phe326Cys)
c.1136T>G (p.Phe379Cys)
15g.38351529C>ACA391934528SPRED1c.1200C>A (p.Phe400Leu)
c.1236C>A (p.Phe412Leu)
c.978C>A (p.Phe326Leu)
c.1137C>A (p.Phe379Leu)
15g.38351529C>GCA391934533SPRED1c.1200C>G (p.Phe400Leu)
c.1236C>G (p.Phe412Leu)
c.978C>G (p.Phe326Leu)
c.1137C>G (p.Phe379Leu)
 gnomAD v4
15g.38351529C>TCA490012537SPRED1c.1200C>T (p.Phe400=)
c.1236C>T (p.Phe412=)
c.978C>T (p.Phe326=)
c.1137C>T (p.Phe379=)
 ClinVar dbSNP
15g.38351530T>ACA391934536SPRED1c.1201T>A (p.Cys401Ser)
c.1237T>A (p.Cys413Ser)
c.979T>A (p.Cys327Ser)
c.1138T>A (p.Cys380Ser)
15g.38351530T>CCA391934534SPRED1c.1201T>C (p.Cys401Arg)
c.1237T>C (p.Cys413Arg)
c.979T>C (p.Cys327Arg)
c.1138T>C (p.Cys380Arg)
 gnomAD v4
15g.38351530T>GCA391934535SPRED1c.1201T>G (p.Cys401Gly)
c.1237T>G (p.Cys413Gly)
c.979T>G (p.Cys327Gly)
c.1138T>G (p.Cys380Gly)
15g.38351533_38351536dupCA658761259SPRED1c.1204_1207dup (p.Arg403LeufsTer30)
c.1240_1243dup (p.Arg415LeufsTer30)
c.982_985dup (p.Arg329LeufsTer30)
c.1141_1144dup (p.Arg382LeufsTer30)
15g.38351531G>ACA391934538SPRED1c.1202G>A (p.Cys401Tyr)
c.1238G>A (p.Cys413Tyr)
c.980G>A (p.Cys327Tyr)
c.1139G>A (p.Cys380Tyr)
15g.38351531G>CCA391934539SPRED1c.1202G>C (p.Cys401Ser)
c.1238G>C (p.Cys413Ser)
c.980G>C (p.Cys327Ser)
c.1139G>C (p.Cys380Ser)
 dbSNP gnomAD v3 gnomAD v4
15g.38351531G=CA2170812751SPRED1c.1202G= (p.Cys401=)
c.1238G= (p.Cys413=)
c.980G= (p.Cys327=)
c.1139G= (p.Cys380=)
15g.38351531G>TCA7470243SPRED1c.1202G>T (p.Cys401Phe)
c.1238G>T (p.Cys413Phe)
c.980G>T (p.Cys327Phe)
c.1139G>T (p.Cys380Phe)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.38351532C>ACA391934541SPRED1c.1203C>A (p.Cys401Ter)
c.1239C>A (p.Cys413Ter)
c.981C>A (p.Cys327Ter)
c.1140C>A (p.Cys380Ter)
15g.38351532C>GCA391934543SPRED1c.1203C>G (p.Cys401Trp)
c.1239C>G (p.Cys413Trp)
c.981C>G (p.Cys327Trp)
c.1140C>G (p.Cys380Trp)
15g.38351532C>TCA490012540SPRED1c.1203C>T (p.Cys401=)
c.1239C>T (p.Cys413=)
c.981C>T (p.Cys327=)
c.1140C>T (p.Cys380=)
 ClinVar dbSNP gnomAD v4
15g.38351533T>ACA391934544SPRED1c.1204T>A (p.Leu402Met)
c.1240T>A (p.Leu414Met)
c.982T>A (p.Leu328Met)
c.1141T>A (p.Leu381Met)
15g.38351533T>CCA7470244SPRED1c.1204T>C (p.Leu402=)
c.1240T>C (p.Leu414=)
c.982T>C (p.Leu328=)
c.1141T>C (p.Leu381=)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.38351533T>GCA391934546SPRED1c.1204T>G (p.Leu402Val)
c.1240T>G (p.Leu414Val)
c.982T>G (p.Leu328Val)
c.1141T>G (p.Leu381Val)
15g.38351533T=CA2170812752SPRED1c.1204T= (p.Leu402=)
c.1240T= (p.Leu414=)
c.982T= (p.Leu328=)
c.1141T= (p.Leu381=)
15g.38351534T>ACA391934548SPRED1c.1205T>A (p.Leu402Ter)
c.1241T>A (p.Leu414Ter)
c.983T>A (p.Leu328Ter)
c.1142T>A (p.Leu381Ter)
15g.38351534T>CCA391934550SPRED1c.1205T>C (p.Leu402Ser)
c.1241T>C (p.Leu414Ser)
c.983T>C (p.Leu328Ser)
c.1142T>C (p.Leu381Ser)
15g.38351534T>GCA391934553SPRED1c.1205T>G (p.Leu402Trp)
c.1241T>G (p.Leu414Trp)
c.983T>G (p.Leu328Trp)
c.1142T>G (p.Leu381Trp)
15g.38351535G>ACA490012542SPRED1c.1206G>A (p.Leu402=)
c.1242G>A (p.Leu414=)
c.984G>A (p.Leu328=)
c.1143G>A (p.Leu381=)
 ClinVar
15g.38351535G>CCA391934555SPRED1c.1206G>C (p.Leu402Phe)
c.1242G>C (p.Leu414Phe)
c.984G>C (p.Leu328Phe)
c.1143G>C (p.Leu381Phe)
15g.38351535G>TCA391934556SPRED1c.1206G>T (p.Leu402Phe)
c.1242G>T (p.Leu414Phe)
c.984G>T (p.Leu328Phe)
c.1143G>T (p.Leu381Phe)
15g.38351535_38351546delCA2501080789SPRED1c.1206_1217del (p.Leu402_Ala406delinsPhe)
c.1242_1253del (p.Leu414_Ala418delinsPhe)
c.984_995del (p.Leu328_Ala332delinsPhe)
c.1143_1154del (p.Leu381_Ala385delinsPhe)
15g.38351536C>ACA490012545SPRED1c.1207C>A (p.Arg403=)
c.1243C>A (p.Arg415=)
c.985C>A (p.Arg329=)
c.1144C>A (p.Arg382=)
15g.38351536C=CA2170812753SPRED1c.1207C= (p.Arg403=)
c.1243C= (p.Arg415=)
c.985C= (p.Arg329=)
c.1144C= (p.Arg382=)
15g.38351536C>GCA391934558SPRED1c.1207C>G (p.Arg403Gly)
c.1243C>G (p.Arg415Gly)
c.985C>G (p.Arg329Gly)
c.1144C>G (p.Arg382Gly)
15g.38351536C>TCA391934560SPRED1c.1207C>T (p.Arg403Ter)
c.1243C>T (p.Arg415Ter)
c.985C>T (p.Arg329Ter)
c.1144C>T (p.Arg382Ter)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.38351537G>ACA7470245SPRED1c.1208G>A (p.Arg403Gln)
c.1244G>A (p.Arg415Gln)
c.986G>A (p.Arg329Gln)
c.1145G>A (p.Arg382Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.38351537G>CCA391934563SPRED1c.1208G>C (p.Arg403Pro)
c.1244G>C (p.Arg415Pro)
c.986G>C (p.Arg329Pro)
c.1145G>C (p.Arg382Pro)
15g.38351537G=CA2170812754SPRED1c.1208G= (p.Arg403=)
c.1244G= (p.Arg415=)
c.986G= (p.Arg329=)
c.1145G= (p.Arg382=)
15g.38351537G>TCA391934561SPRED1c.1208G>T (p.Arg403Leu)
c.1244G>T (p.Arg415Leu)
c.986G>T (p.Arg329Leu)
c.1145G>T (p.Arg382Leu)
 dbSNP gnomAD v2 gnomAD v4

Number of alleles fetched