Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.38351450_38351474delCA2575673317SPRED1c.1121_1145del (p.Ser374ThrfsTer24)
c.1157_1181del (p.Ser386ThrfsTer24)
c.899_923del (p.Ser300ThrfsTer24)
c.1058_1082del (p.Ser353ThrfsTer24)
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
15g.38351538A>CCA490012553SPRED1c.1209A>C (p.Arg403=)
c.1245A>C (p.Arg415=)
c.987A>C (p.Arg329=)
c.1146A>C (p.Arg382=)
15g.38351538A>GCA490012552SPRED1c.1209A>G (p.Arg403=)
c.1245A>G (p.Arg415=)
c.987A>G (p.Arg329=)
c.1146A>G (p.Arg382=)
15g.38351538A>TCA490012551SPRED1c.1209A>T (p.Arg403=)
c.1245A>T (p.Arg415=)
c.987A>T (p.Arg329=)
c.1146A>T (p.Arg382=)
15g.38351539T>ACA391934565SPRED1c.1210T>A (p.Trp404Arg)
c.1246T>A (p.Trp416Arg)
c.988T>A (p.Trp330Arg)
c.1147T>A (p.Trp383Arg)
15g.38351539T>CCA391934568SPRED1c.1210T>C (p.Trp404Arg)
c.1246T>C (p.Trp416Arg)
c.988T>C (p.Trp330Arg)
c.1147T>C (p.Trp383Arg)
15g.38351539T>GCA7470246SPRED1c.1210T>G (p.Trp404Gly)
c.1246T>G (p.Trp416Gly)
c.988T>G (p.Trp330Gly)
c.1147T>G (p.Trp383Gly)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.38351539T=CA2170812755SPRED1c.1210T= (p.Trp404=)
c.1246T= (p.Trp416=)
c.988T= (p.Trp330=)
c.1147T= (p.Trp383=)
15g.38351540G>ACA391934569SPRED1c.1211G>A (p.Trp404Ter)
c.1247G>A (p.Trp416Ter)
c.989G>A (p.Trp330Ter)
c.1148G>A (p.Trp383Ter)
 ClinVar dbSNP
15g.38351540G>CCA391934571SPRED1c.1211G>C (p.Trp404Ser)
c.1247G>C (p.Trp416Ser)
c.989G>C (p.Trp330Ser)
c.1148G>C (p.Trp383Ser)
15g.38351540G=CA2170812756SPRED1c.1211G= (p.Trp404=)
c.1247G= (p.Trp416=)
c.989G= (p.Trp330=)
c.1148G= (p.Trp383=)
15g.38351540G>TCA391934570SPRED1c.1211G>T (p.Trp404Leu)
c.1247G>T (p.Trp416Leu)
c.989G>T (p.Trp330Leu)
c.1148G>T (p.Trp383Leu)
15g.38351541G>ACA391934572SPRED1c.1212G>A (p.Trp404Ter)
c.1248G>A (p.Trp416Ter)
c.990G>A (p.Trp330Ter)
c.1149G>A (p.Trp383Ter)
15g.38351541G>CCA391934573SPRED1c.1212G>C (p.Trp404Cys)
c.1248G>C (p.Trp416Cys)
c.990G>C (p.Trp330Cys)
c.1149G>C (p.Trp383Cys)
15g.38351541G>TCA391934575SPRED1c.1212G>T (p.Trp404Cys)
c.1248G>T (p.Trp416Cys)
c.990G>T (p.Trp330Cys)
c.1149G>T (p.Trp383Cys)
15g.38351542T>ACA391934577SPRED1c.1213T>A (p.Leu405Ile)
c.1249T>A (p.Leu417Ile)
c.991T>A (p.Leu331Ile)
c.1150T>A (p.Leu384Ile)
15g.38351542T>CCA490012558SPRED1c.1213T>C (p.Leu405=)
c.1249T>C (p.Leu417=)
c.991T>C (p.Leu331=)
c.1150T>C (p.Leu384=)
15g.38351542T>GCA391934578SPRED1c.1213T>G (p.Leu405Val)
c.1249T>G (p.Leu417Val)
c.991T>G (p.Leu331Val)
c.1150T>G (p.Leu384Val)
15g.38351543T>ACA391934580SPRED1c.1214T>A (p.Leu405Ter)
c.1250T>A (p.Leu417Ter)
c.992T>A (p.Leu331Ter)
c.1151T>A (p.Leu384Ter)
15g.38351543T>CCA391934582SPRED1c.1214T>C (p.Leu405Ser)
c.1250T>C (p.Leu417Ser)
c.992T>C (p.Leu331Ser)
c.1151T>C (p.Leu384Ser)
15g.38351543T>GCA391934583SPRED1c.1214T>G (p.Leu405Ter)
c.1250T>G (p.Leu417Ter)
c.992T>G (p.Leu331Ter)
c.1151T>G (p.Leu384Ter)
15g.38351544A=CA2170812757SPRED1c.1215A= (p.Leu405=)
c.1251A= (p.Leu417=)
c.993A= (p.Leu331=)
c.1152A= (p.Leu384=)
15g.38351544A>CCA391934585SPRED1c.1215A>C (p.Leu405Phe)
c.1251A>C (p.Leu417Phe)
c.993A>C (p.Leu331Phe)
c.1152A>C (p.Leu384Phe)
15g.38351544A>GCA490012561SPRED1c.1215A>G (p.Leu405=)
c.1251A>G (p.Leu417=)
c.993A>G (p.Leu331=)
c.1152A>G (p.Leu384=)
 ClinVar dbSNP gnomAD v4
15g.38351544A>TCA391934587SPRED1c.1215A>T (p.Leu405Phe)
c.1251A>T (p.Leu417Phe)
c.993A>T (p.Leu331Phe)
c.1152A>T (p.Leu384Phe)
15g.38351545G>ACA7470247SPRED1c.1216G>A (p.Ala406Thr)
c.1252G>A (p.Ala418Thr)
c.994G>A (p.Ala332Thr)
c.1153G>A (p.Ala385Thr)
 ClinVar dbSNP ExAC gnomAD v2
15g.38351545G>CCA391934589SPRED1c.1216G>C (p.Ala406Pro)
c.1252G>C (p.Ala418Pro)
c.994G>C (p.Ala332Pro)
c.1153G>C (p.Ala385Pro)
15g.38351545G=CA2170812758SPRED1c.1216G= (p.Ala406=)
c.1252G= (p.Ala418=)
c.994G= (p.Ala332=)
c.1153G= (p.Ala385=)
15g.38351545G>TCA391934591SPRED1c.1216G>T (p.Ala406Ser)
c.1252G>T (p.Ala418Ser)
c.994G>T (p.Ala332Ser)
c.1153G>T (p.Ala385Ser)
 gnomAD v4
15g.38351546C>ACA391934595SPRED1c.1217C>A (p.Ala406Asp)
c.1253C>A (p.Ala418Asp)
c.995C>A (p.Ala332Asp)
c.1154C>A (p.Ala385Asp)
15g.38351546C=CA2170812759SPRED1c.1217C= (p.Ala406=)
c.1253C= (p.Ala418=)
c.995C= (p.Ala332=)
c.1154C= (p.Ala385=)
15g.38351546C>GCA391934593SPRED1c.1217C>G (p.Ala406Gly)
c.1253C>G (p.Ala418Gly)
c.995C>G (p.Ala332Gly)
c.1154C>G (p.Ala385Gly)
15g.38351546C>TCA7470248SPRED1c.1217C>T (p.Ala406Val)
c.1253C>T (p.Ala418Val)
c.995C>T (p.Ala332Val)
c.1154C>T (p.Ala385Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.38351547C>ACA490012562SPRED1c.1218C>A (p.Ala406=)
c.1254C>A (p.Ala418=)
c.996C>A (p.Ala332=)
c.1155C>A (p.Ala385=)
15g.38351547C>GCA490012563SPRED1c.1218C>G (p.Ala406=)
c.1254C>G (p.Ala418=)
c.996C>G (p.Ala332=)
c.1155C>G (p.Ala385=)
15g.38351547C>TCA490012564SPRED1c.1218C>T (p.Ala406=)
c.1254C>T (p.Ala418=)
c.996C>T (p.Ala332=)
c.1155C>T (p.Ala385=)
15g.38351548C>ACA391934597SPRED1c.1219C>A (p.Leu407Met)
c.1255C>A (p.Leu419Met)
c.997C>A (p.Leu333Met)
c.1156C>A (p.Leu386Met)
 dbSNP gnomAD v2 gnomAD v4
15g.38351548C=CA2170812760SPRED1c.1219C= (p.Leu407=)
c.1255C= (p.Leu419=)
c.997C= (p.Leu333=)
c.1156C= (p.Leu386=)
15g.38351548C>GCA391934599SPRED1c.1219C>G (p.Leu407Val)
c.1255C>G (p.Leu419Val)
c.997C>G (p.Leu333Val)
c.1156C>G (p.Leu386Val)
15g.38351548C>TCA490012566SPRED1c.1219C>T (p.Leu407=)
c.1255C>T (p.Leu419=)
c.997C>T (p.Leu333=)
c.1156C>T (p.Leu386=)
15g.38351549T>ACA391934600SPRED1c.1220T>A (p.Leu407Gln)
c.1256T>A (p.Leu419Gln)
c.998T>A (p.Leu333Gln)
c.1157T>A (p.Leu386Gln)
15g.38351549T>CCA391934601SPRED1c.1220T>C (p.Leu407Pro)
c.1256T>C (p.Leu419Pro)
c.998T>C (p.Leu333Pro)
c.1157T>C (p.Leu386Pro)
 dbSNP gnomAD v2 gnomAD v4
15g.38351549T>GCA391934603SPRED1c.1220T>G (p.Leu407Arg)
c.1256T>G (p.Leu419Arg)
c.998T>G (p.Leu333Arg)
c.1157T>G (p.Leu386Arg)
15g.38351549T=CA2170812761SPRED1c.1220T= (p.Leu407=)
c.1256T= (p.Leu419=)
c.998T= (p.Leu333=)
c.1157T= (p.Leu386=)
15g.38351550G>ACA490012570SPRED1c.1221G>A (p.Leu407=)
c.1257G>A (p.Leu419=)
c.999G>A (p.Leu333=)
c.1158G>A (p.Leu386=)
15g.38351550G>CCA490012571SPRED1c.1221G>C (p.Leu407=)
c.1257G>C (p.Leu419=)
c.999G>C (p.Leu333=)
c.1158G>C (p.Leu386=)
15g.38351550G>TCA490012572SPRED1c.1221G>T (p.Leu407=)
c.1257G>T (p.Leu419=)
c.999G>T (p.Leu333=)
c.1158G>T (p.Leu386=)
15g.38351550_38351571delCA2513772032SPRED1c.1221_1242del (p.Val408HisfsTer9)
c.1257_1278del (p.Val420HisfsTer9)
c.999_1020del (p.Val334HisfsTer9)
c.1158_1179del (p.Val387HisfsTer9)
15g.38351551G>ACA391934606SPRED1c.1222G>A (p.Val408Ile)
c.1258G>A (p.Val420Ile)
c.1000G>A (p.Val334Ile)
c.1159G>A (p.Val387Ile)
 gnomAD v4
15g.38351551G>CCA391934609SPRED1c.1222G>C (p.Val408Leu)
c.1258G>C (p.Val420Leu)
c.1000G>C (p.Val334Leu)
c.1159G>C (p.Val387Leu)
15g.38351551G=CA2170812762SPRED1c.1222G= (p.Val408=)
c.1258G= (p.Val420=)
c.1000G= (p.Val334=)
c.1159G= (p.Val387=)
15g.38351551G>TCA7470249SPRED1c.1222G>T (p.Val408Leu)
c.1258G>T (p.Val420Leu)
c.1000G>T (p.Val334Leu)
c.1159G>T (p.Val387Leu)
 dbSNP ExAC gnomAD v2
15g.38351552T>ACA391934610SPRED1c.1223T>A (p.Val408Glu)
c.1259T>A (p.Val420Glu)
c.1001T>A (p.Val334Glu)
c.1160T>A (p.Val387Glu)
15g.38351552T>CCA391934612SPRED1c.1223T>C (p.Val408Ala)
c.1259T>C (p.Val420Ala)
c.1001T>C (p.Val334Ala)
c.1160T>C (p.Val387Ala)
15g.38351552T>GCA391934613SPRED1c.1223T>G (p.Val408Gly)
c.1259T>G (p.Val420Gly)
c.1001T>G (p.Val334Gly)
c.1160T>G (p.Val387Gly)
15g.38351553delCA2697554337SPRED1c.1224del (p.Ala409LeufsTer15)
c.1260del (p.Ala421LeufsTer15)
c.1002del (p.Ala335LeufsTer15)
c.1161del (p.Ala388LeufsTer15)
 ClinVar
15g.38351553A=CA2170812763SPRED1c.1224A= (p.Val408=)
c.1260A= (p.Val420=)
c.1002A= (p.Val334=)
c.1161A= (p.Val387=)
15g.38351553A>CCA490012575SPRED1c.1224A>C (p.Val408=)
c.1260A>C (p.Val420=)
c.1002A>C (p.Val334=)
c.1161A>C (p.Val387=)
15g.38351553A>GCA490012576SPRED1c.1224A>G (p.Val408=)
c.1260A>G (p.Val420=)
c.1002A>G (p.Val334=)
c.1161A>G (p.Val387=)
 ClinVar dbSNP gnomAD v4
15g.38351553A>TCA490012577SPRED1c.1224A>T (p.Val408=)
c.1260A>T (p.Val420=)
c.1002A>T (p.Val334=)
c.1161A>T (p.Val387=)
15g.38351554G>ACA7470251SPRED1c.1225G>A (p.Ala409Thr)
c.1261G>A (p.Ala421Thr)
c.1003G>A (p.Ala335Thr)
c.1162G>A (p.Ala388Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.38351554G>CCA391934616SPRED1c.1225G>C (p.Ala409Pro)
c.1261G>C (p.Ala421Pro)
c.1003G>C (p.Ala335Pro)
c.1162G>C (p.Ala388Pro)
15g.38351554G=CA2170812764SPRED1c.1225G= (p.Ala409=)
c.1261G= (p.Ala421=)
c.1003G= (p.Ala335=)
c.1162G= (p.Ala388=)
15g.38351554G>TCA7470250SPRED1c.1225G>T (p.Ala409Ser)
c.1261G>T (p.Ala421Ser)
c.1003G>T (p.Ala335Ser)
c.1162G>T (p.Ala388Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.38351554_38351555delinsTTCA658824654SPRED1c.1225_1226delinsTT (p.Ala409Phe)
c.1261_1262delinsTT (p.Ala421Phe)
c.1003_1004delinsTT (p.Ala335Phe)
c.1162_1163delinsTT (p.Ala388Phe)
 ClinVar
15g.38351555C>ACA391934619SPRED1c.1226C>A (p.Ala409Asp)
c.1262C>A (p.Ala421Asp)
c.1004C>A (p.Ala335Asp)
c.1163C>A (p.Ala388Asp)
15g.38351555C=CA2170812765SPRED1c.1226C= (p.Ala409=)
c.1262C= (p.Ala421=)
c.1004C= (p.Ala335=)
c.1163C= (p.Ala388=)
15g.38351555C>GCA391934621SPRED1c.1226C>G (p.Ala409Gly)
c.1262C>G (p.Ala421Gly)
c.1004C>G (p.Ala335Gly)
c.1163C>G (p.Ala388Gly)
15g.38351555C>TCA7470252SPRED1c.1226C>T (p.Ala409Val)
c.1262C>T (p.Ala421Val)
c.1004C>T (p.Ala335Val)
c.1163C>T (p.Ala388Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.38351556T>ACA490012582SPRED1c.1227T>A (p.Ala409=)
c.1263T>A (p.Ala421=)
c.1005T>A (p.Ala335=)
c.1164T>A (p.Ala388=)
15g.38351556T>CCA490012583SPRED1c.1227T>C (p.Ala409=)
c.1263T>C (p.Ala421=)
c.1005T>C (p.Ala335=)
c.1164T>C (p.Ala388=)
15g.38351556T>GCA490012581SPRED1c.1227T>G (p.Ala409=)
c.1263T>G (p.Ala421=)
c.1005T>G (p.Ala335=)
c.1164T>G (p.Ala388=)
 gnomAD v4
15g.38351557T>ACA391934622SPRED1c.1228T>A (p.Leu410Met)
c.1264T>A (p.Leu422Met)
c.1006T>A (p.Leu336Met)
c.1165T>A (p.Leu389Met)
15g.38351557T>CCA490012584SPRED1c.1228T>C (p.Leu410=)
c.1264T>C (p.Leu422=)
c.1006T>C (p.Leu336=)
c.1165T>C (p.Leu389=)
15g.38351557T>GCA391934623SPRED1c.1228T>G (p.Leu410Val)
c.1264T>G (p.Leu422Val)
c.1006T>G (p.Leu336Val)
c.1165T>G (p.Leu389Val)
15g.38351561_38351570delCA2499222899SPRED1c.1232_1241del (p.Ser411TyrfsTer10)
c.1268_1277del (p.Ser423TyrfsTer10)
c.1010_1019del (p.Ser337TyrfsTer10)
c.1169_1178del (p.Ser390TyrfsTer10)
 ClinVar dbSNP
15g.38351558T>ACA391934625SPRED1c.1229T>A (p.Leu410Ter)
c.1265T>A (p.Leu422Ter)
c.1007T>A (p.Leu336Ter)
c.1166T>A (p.Leu389Ter)
15g.38351558T>CCA391934627SPRED1c.1229T>C (p.Leu410Ser)
c.1265T>C (p.Leu422Ser)
c.1007T>C (p.Leu336Ser)
c.1166T>C (p.Leu389Ser)
 dbSNP gnomAD v3 gnomAD v4
15g.38351558T>GCA391934628SPRED1c.1229T>G (p.Leu410Trp)
c.1265T>G (p.Leu422Trp)
c.1007T>G (p.Leu336Trp)
c.1166T>G (p.Leu389Trp)
15g.38351558T=CA2170812766SPRED1c.1229T= (p.Leu410=)
c.1265T= (p.Leu422=)
c.1007T= (p.Leu336=)
c.1166T= (p.Leu389=)
15g.38351559G>ACA490012586SPRED1c.1230G>A (p.Leu410=)
c.1266G>A (p.Leu422=)
c.1008G>A (p.Leu336=)
c.1167G>A (p.Leu389=)
15g.38351559G>CCA391934630SPRED1c.1230G>C (p.Leu410Phe)
c.1266G>C (p.Leu422Phe)
c.1008G>C (p.Leu336Phe)
c.1167G>C (p.Leu389Phe)
15g.38351559G>TCA391934631SPRED1c.1230G>T (p.Leu410Phe)
c.1266G>T (p.Leu422Phe)
c.1008G>T (p.Leu336Phe)
c.1167G>T (p.Leu389Phe)
15g.38351560T>ACA391934633SPRED1c.1231T>A (p.Ser411Thr)
c.1267T>A (p.Ser423Thr)
c.1009T>A (p.Ser337Thr)
c.1168T>A (p.Ser390Thr)
15g.38351560T>CCA391934635SPRED1c.1231T>C (p.Ser411Pro)
c.1267T>C (p.Ser423Pro)
c.1009T>C (p.Ser337Pro)
c.1168T>C (p.Ser390Pro)
 ClinVar
15g.38351560T>GCA391934637SPRED1c.1231T>G (p.Ser411Ala)
c.1267T>G (p.Ser423Ala)
c.1009T>G (p.Ser337Ala)
c.1168T>G (p.Ser390Ala)
15g.38351561C>ACA391934638SPRED1c.1232C>A (p.Ser411Tyr)
c.1268C>A (p.Ser423Tyr)
c.1010C>A (p.Ser337Tyr)
c.1169C>A (p.Ser390Tyr)
15g.38351561C>GCA391934641SPRED1c.1232C>G (p.Ser411Cys)
c.1268C>G (p.Ser423Cys)
c.1010C>G (p.Ser337Cys)
c.1169C>G (p.Ser390Cys)
 ClinVar gnomAD v4
15g.38351561C>TCA391934643SPRED1c.1232C>T (p.Ser411Phe)
c.1268C>T (p.Ser423Phe)
c.1010C>T (p.Ser337Phe)
c.1169C>T (p.Ser390Phe)
 ClinVar
15g.38351562T>ACA490012593SPRED1c.1233T>A (p.Ser411=)
c.1269T>A (p.Ser423=)
c.1011T>A (p.Ser337=)
c.1170T>A (p.Ser390=)
15g.38351562T>CCA490012591SPRED1c.1233T>C (p.Ser411=)
c.1269T>C (p.Ser423=)
c.1011T>C (p.Ser337=)
c.1170T>C (p.Ser390=)
15g.38351562T>GCA490012590SPRED1c.1233T>G (p.Ser411=)
c.1269T>G (p.Ser423=)
c.1011T>G (p.Ser337=)
c.1170T>G (p.Ser390=)
15g.38351564dupCA2580089340SPRED1c.1235dup (p.Ile413HisfsTer19)
c.1271dup (p.Ile425HisfsTer19)
c.1013dup (p.Ile339HisfsTer19)
c.1172dup (p.Ile392HisfsTer19)
 ClinVar
15g.38351563T>ACA391934645SPRED1c.1234T>A (p.Phe412Ile)
c.1270T>A (p.Phe424Ile)
c.1012T>A (p.Phe338Ile)
c.1171T>A (p.Phe391Ile)
15g.38351563T>CCA391934647SPRED1c.1234T>C (p.Phe412Leu)
c.1270T>C (p.Phe424Leu)
c.1012T>C (p.Phe338Leu)
c.1171T>C (p.Phe391Leu)
15g.38351563T>GCA391934646SPRED1c.1234T>G (p.Phe412Val)
c.1270T>G (p.Phe424Val)
c.1012T>G (p.Phe338Val)
c.1171T>G (p.Phe391Val)
15g.38351564T>ACA391934648SPRED1c.1235T>A (p.Phe412Tyr)
c.1271T>A (p.Phe424Tyr)
c.1013T>A (p.Phe338Tyr)
c.1172T>A (p.Phe391Tyr)
15g.38351564T>CCA391934649SPRED1c.1235T>C (p.Phe412Ser)
c.1271T>C (p.Phe424Ser)
c.1013T>C (p.Phe338Ser)
c.1172T>C (p.Phe391Ser)
15g.38351564T>GCA391934650SPRED1c.1235T>G (p.Phe412Cys)
c.1271T>G (p.Phe424Cys)
c.1013T>G (p.Phe338Cys)
c.1172T>G (p.Phe391Cys)
15g.38351565C>ACA391934651SPRED1c.1236C>A (p.Phe412Leu)
c.1272C>A (p.Phe424Leu)
c.1014C>A (p.Phe338Leu)
c.1173C>A (p.Phe391Leu)
15g.38351565C>GCA391934652SPRED1c.1236C>G (p.Phe412Leu)
c.1272C>G (p.Phe424Leu)
c.1014C>G (p.Phe338Leu)
c.1173C>G (p.Phe391Leu)
 gnomAD v4
15g.38351565C>TCA490012595SPRED1c.1236C>T (p.Phe412=)
c.1272C>T (p.Phe424=)
c.1014C>T (p.Phe338=)
c.1173C>T (p.Phe391=)
 gnomAD v4 COSMIC
15g.38351566A>CCA391934653SPRED1c.1237A>C (p.Ile413Leu)
c.1273A>C (p.Ile425Leu)
c.1015A>C (p.Ile339Leu)
c.1174A>C (p.Ile392Leu)
15g.38351566A>GCA391934654SPRED1c.1237A>G (p.Ile413Val)
c.1273A>G (p.Ile425Val)
c.1015A>G (p.Ile339Val)
c.1174A>G (p.Ile392Val)
 gnomAD v4
15g.38351566A>TCA391934655SPRED1c.1237A>T (p.Ile413Phe)
c.1273A>T (p.Ile425Phe)
c.1015A>T (p.Ile339Phe)
c.1174A>T (p.Ile392Phe)
15g.38351566_38351567delCA2573150675SPRED1c.1237_1238del (p.Ile413CysfsTer18)
c.1273_1274del (p.Ile425CysfsTer18)
c.1015_1016del (p.Ile339CysfsTer18)
c.1174_1175del (p.Ile392CysfsTer18)
 ClinVar dbSNP
15g.38351567T>ACA391934656SPRED1c.1238T>A (p.Ile413Asn)
c.1274T>A (p.Ile425Asn)
c.1016T>A (p.Ile339Asn)
c.1175T>A (p.Ile392Asn)
15g.38351567T>CCA391934657SPRED1c.1238T>C (p.Ile413Thr)
c.1274T>C (p.Ile425Thr)
c.1016T>C (p.Ile339Thr)
c.1175T>C (p.Ile392Thr)
 ClinVar dbSNP gnomAD v3 gnomAD v4
15g.38351567T>GCA391934658SPRED1c.1238T>G (p.Ile413Ser)
c.1274T>G (p.Ile425Ser)
c.1016T>G (p.Ile339Ser)
c.1175T>G (p.Ile392Ser)
15g.38351567T=CA2170812767SPRED1c.1238T= (p.Ile413=)
c.1274T= (p.Ile425=)
c.1016T= (p.Ile339=)
c.1175T= (p.Ile392=)
15g.38351568T>ACA490012597SPRED1c.1239T>A (p.Ile413=)
c.1275T>A (p.Ile425=)
c.1017T>A (p.Ile339=)
c.1176T>A (p.Ile392=)
15g.38351568T>CCA7470253SPRED1c.1239T>C (p.Ile413=)
c.1275T>C (p.Ile425=)
c.1017T>C (p.Ile339=)
c.1176T>C (p.Ile392=)
 dbSNP ExAC
15g.38351568T>GCA391934659SPRED1c.1239T>G (p.Ile413Met)
c.1275T>G (p.Ile425Met)
c.1017T>G (p.Ile339Met)
c.1176T>G (p.Ile392Met)
15g.38351568T=CA2170812768SPRED1c.1239T= (p.Ile413=)
c.1275T= (p.Ile425=)
c.1017T= (p.Ile339=)
c.1176T= (p.Ile392=)
15g.38351569G>ACA391934660SPRED1c.1240G>A (p.Val414Ile)
c.1276G>A (p.Val426Ile)
c.1018G>A (p.Val340Ile)
c.1177G>A (p.Val393Ile)
 gnomAD v4
15g.38351569G>CCA391934662SPRED1c.1240G>C (p.Val414Leu)
c.1276G>C (p.Val426Leu)
c.1018G>C (p.Val340Leu)
c.1177G>C (p.Val393Leu)
15g.38351569G>TCA391934661SPRED1c.1240G>T (p.Val414Leu)
c.1276G>T (p.Val426Leu)
c.1018G>T (p.Val340Leu)
c.1177G>T (p.Val393Leu)
15g.38351570T>ACA391934663SPRED1c.1241T>A (p.Val414Glu)
c.1277T>A (p.Val426Glu)
c.1019T>A (p.Val340Glu)
c.1178T>A (p.Val393Glu)
15g.38351570T>CCA391934664SPRED1c.1241T>C (p.Val414Ala)
c.1277T>C (p.Val426Ala)
c.1019T>C (p.Val340Ala)
c.1178T>C (p.Val393Ala)
15g.38351570T>GCA391934665SPRED1c.1241T>G (p.Val414Gly)
c.1277T>G (p.Val426Gly)
c.1019T>G (p.Val340Gly)
c.1178T>G (p.Val393Gly)
15g.38351571A=CA2170812769SPRED1c.1242A= (p.Val414=)
c.1278A= (p.Val426=)
c.1020A= (p.Val340=)
c.1179A= (p.Val393=)
15g.38351571A>CCA269293463SPRED1c.1242A>C (p.Val414=)
c.1278A>C (p.Val426=)
c.1020A>C (p.Val340=)
c.1179A>C (p.Val393=)
 dbSNP gnomAD v2 gnomAD v4
15g.38351571A>GCA490012601SPRED1c.1242A>G (p.Val414=)
c.1278A>G (p.Val426=)
c.1020A>G (p.Val340=)
c.1179A>G (p.Val393=)
 ClinVar dbSNP
15g.38351571A>TCA490012602SPRED1c.1242A>T (p.Val414=)
c.1278A>T (p.Val426=)
c.1020A>T (p.Val340=)
c.1179A>T (p.Val393=)
15g.38351572C>ACA391934666SPRED1c.1243C>A (p.Pro415Thr)
c.1279C>A (p.Pro427Thr)
c.1021C>A (p.Pro341Thr)
c.1180C>A (p.Pro394Thr)
15g.38351572C>GCA391934667SPRED1c.1243C>G (p.Pro415Ala)
c.1279C>G (p.Pro427Ala)
c.1021C>G (p.Pro341Ala)
c.1180C>G (p.Pro394Ala)
15g.38351572C>TCA391934668SPRED1c.1243C>T (p.Pro415Ser)
c.1279C>T (p.Pro427Ser)
c.1021C>T (p.Pro341Ser)
c.1180C>T (p.Pro394Ser)
15g.38351573C>ACA391934669SPRED1c.1244C>A (p.Pro415Gln)
c.1280C>A (p.Pro427Gln)
c.1022C>A (p.Pro341Gln)
c.1181C>A (p.Pro394Gln)
15g.38351573C>GCA391934670SPRED1c.1244C>G (p.Pro415Arg)
c.1280C>G (p.Pro427Arg)
c.1022C>G (p.Pro341Arg)
c.1181C>G (p.Pro394Arg)
15g.38351573C>TCA391934671SPRED1c.1244C>T (p.Pro415Leu)
c.1280C>T (p.Pro427Leu)
c.1022C>T (p.Pro341Leu)
c.1181C>T (p.Pro394Leu)

Number of alleles fetched