Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.136114879_136114943del | CA891841793 | CXCR4 | c.976_1040del (p.Ser326GlnfsTer6) c.943_1007del (p.Ser315GlnfsTer6) c.988_1052del (p.Ser330GlnfsTer6) c.1000_1064del (p.Ser334GlnfsTer6) n.1182_1246del c.1201_1265del (p.Ser401GlnfsTer6) c.1087_1151del (p.Ser363GlnfsTer6) | |
2 | g.136114900_136115041dup | CA2573133307 | CXCR4 | c.881_1022dup (p.Ser342ProfsTer12) c.848_989dup (p.Ser331ProfsTer12) c.893_1034dup (p.Ser346ProfsTer12) c.905_1046dup (p.Ser350ProfsTer12) n.1087_1228dup c.1106_1247dup (p.Ser417ProfsTer12) c.992_1133dup (p.Ser379ProfsTer12) | ClinVar dbSNP |
2 | g.136114916_136114919dup | CA2573051654 | CXCR4 | c.1000_1003dup (p.Ser335PhefsTer6) c.967_970dup (p.Ser324PhefsTer6) c.1012_1015dup (p.Ser339PhefsTer6) c.1024_1027dup (p.Ser343PhefsTer6) n.1206_1209dup c.1225_1228dup (p.Ser410PhefsTer6) c.1111_1114dup (p.Ser372PhefsTer6) | ClinVar dbSNP |
2 | g.136114916_136114919del | CA645539211 | CXCR4 | c.1000_1003del (p.Ser334LeufsTer27) c.967_970del (p.Ser323LeufsTer27) c.1012_1015del (p.Ser338LeufsTer27) c.1024_1027del (p.Ser342LeufsTer27) n.1206_1209del c.1225_1228del (p.Ser409LeufsTer27) c.1111_1114del (p.Ser371LeufsTer27) | COSMIC COSMIC |
2 | g.136114915G>A | CA348657409 | CXCR4 | c.1001C>T (p.Ser334Leu) c.968C>T (p.Ser323Leu) c.1013C>T (p.Ser338Leu) c.1025C>T (p.Ser342Leu) n.1207C>T c.1226C>T (p.Ser409Leu) c.1112C>T (p.Ser371Leu) | |
2 | g.136114915G>C | CA123717 | CXCR4 | c.1001C>G (p.Ser334Ter) c.968C>G (p.Ser323Ter) c.1013C>G (p.Ser338Ter) c.1025C>G (p.Ser342Ter) n.1207C>G c.1226C>G (p.Ser409Ter) c.1112C>G (p.Ser371Ter) | ClinVar dbSNP COSMIC |
2 | g.136114915G= | CA1290965875 | CXCR4 | c.1001C= (p.Ser334=) c.968C= (p.Ser323=) c.1013C= (p.Ser338=) c.1025C= (p.Ser342=) n.1207C= c.1226C= (p.Ser409=) c.1112C= (p.Ser371=) | |
2 | g.136114915G>T | CA348657412 | CXCR4 | c.1001C>A (p.Ser334Ter) c.968C>A (p.Ser323Ter) c.1013C>A (p.Ser338Ter) c.1025C>A (p.Ser342Ter) n.1207C>A c.1226C>A (p.Ser409Ter) c.1112C>A (p.Ser371Ter) | ClinVar dbSNP gnomAD v4 COSMIC |
2 | g.136114916A>C | CA348657414 | CXCR4 | c.1000T>G (p.Ser334Ala) c.967T>G (p.Ser323Ala) c.1012T>G (p.Ser338Ala) c.1024T>G (p.Ser342Ala) n.1206T>G c.1225T>G (p.Ser409Ala) c.1111T>G (p.Ser371Ala) | |
2 | g.136114916A>G | CA348657416 | CXCR4 | c.1000T>C (p.Ser334Pro) c.967T>C (p.Ser323Pro) c.1012T>C (p.Ser338Pro) c.1024T>C (p.Ser342Pro) n.1206T>C c.1225T>C (p.Ser409Pro) c.1111T>C (p.Ser371Pro) | |
2 | g.136114916A>T | CA348657417 | CXCR4 | c.1000T>A (p.Ser334Thr) c.967T>A (p.Ser323Thr) c.1012T>A (p.Ser338Thr) c.1024T>A (p.Ser342Thr) n.1206T>A c.1225T>A (p.Ser409Thr) c.1111T>A (p.Ser371Thr) | |
2 | g.136114917dup | CA645539213 | CXCR4 | c.1000dup (p.Ser334PhefsTer6) c.967dup (p.Ser323PhefsTer6) c.1012dup (p.Ser338PhefsTer6) c.1024dup (p.Ser342PhefsTer6) n.1206dup c.1225dup (p.Ser409PhefsTer6) c.1111dup (p.Ser371PhefsTer6) | COSMIC |
2 | g.136114917del | CA645539214 | CXCR4 | c.1000del (p.Ser334HisfsTer28) c.967del (p.Ser323HisfsTer28) c.1012del (p.Ser338HisfsTer28) c.1024del (p.Ser342HisfsTer28) n.1206del c.1225del (p.Ser409HisfsTer28) c.1111del (p.Ser371HisfsTer28) | COSMIC |
2 | g.136114917A= | CA1290965876 | CXCR4 | c.999T= (p.His333=) c.966T= (p.His322=) c.1011T= (p.His337=) c.1023T= (p.His341=) n.1205T= c.1224T= (p.His408=) c.1110T= (p.His370=) | |
2 | g.136114917A>C | CA348657419 | CXCR4 | c.999T>G (p.His333Gln) c.966T>G (p.His322Gln) c.1011T>G (p.His337Gln) c.1023T>G (p.His341Gln) n.1205T>G c.1224T>G (p.His408Gln) c.1110T>G (p.His370Gln) | |
2 | g.136114917A>G | CA429191813 | CXCR4 | c.999T>C (p.His333=) c.966T>C (p.His322=) c.1011T>C (p.His337=) c.1023T>C (p.His341=) n.1205T>C c.1224T>C (p.His408=) c.1110T>C (p.His370=) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.136114917A>T | CA348657421 | CXCR4 | c.999T>A (p.His333Gln) c.966T>A (p.His322Gln) c.1011T>A (p.His337Gln) c.1023T>A (p.His341Gln) n.1205T>A c.1224T>A (p.His408Gln) c.1110T>A (p.His370Gln) | |
2 | g.136114918T>A | CA348657424 | CXCR4 | c.998A>T (p.His333Leu) c.965A>T (p.His322Leu) c.1010A>T (p.His337Leu) c.1022A>T (p.His341Leu) n.1204A>T c.1223A>T (p.His408Leu) c.1109A>T (p.His370Leu) | |
2 | g.136114918T>C | CA1890053 | CXCR4 | c.998A>G (p.His333Arg) c.965A>G (p.His322Arg) c.1010A>G (p.His337Arg) c.1022A>G (p.His341Arg) n.1204A>G c.1223A>G (p.His408Arg) c.1109A>G (p.His370Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.136114918T>G | CA348657426 | CXCR4 | c.998A>C (p.His333Pro) c.965A>C (p.His322Pro) c.1010A>C (p.His337Pro) c.1022A>C (p.His341Pro) n.1204A>C c.1223A>C (p.His408Pro) c.1109A>C (p.His370Pro) | |
2 | g.136114918T= | CA1290965877 | CXCR4 | c.998A= (p.His333=) c.965A= (p.His322=) c.1010A= (p.His337=) c.1022A= (p.His341=) n.1204A= c.1223A= (p.His408=) c.1109A= (p.His370=) | |
2 | g.136114919G>A | CA348657429 | CXCR4 | c.997C>T (p.His333Tyr) c.964C>T (p.His322Tyr) c.1009C>T (p.His337Tyr) c.1021C>T (p.His341Tyr) n.1203C>T c.1222C>T (p.His408Tyr) c.1108C>T (p.His370Tyr) | |
2 | g.136114919G>C | CA348657431 | CXCR4 | c.997C>G (p.His333Asp) c.964C>G (p.His322Asp) c.1009C>G (p.His337Asp) c.1021C>G (p.His341Asp) n.1203C>G c.1222C>G (p.His408Asp) c.1108C>G (p.His370Asp) | |
2 | g.136114919G>T | CA348657433 | CXCR4 | c.997C>A (p.His333Asn) c.964C>A (p.His322Asn) c.1009C>A (p.His337Asn) c.1021C>A (p.His341Asn) n.1203C>A c.1222C>A (p.His408Asn) c.1108C>A (p.His370Asn) | |
2 | g.136114920T>A | CA429191817 | CXCR4 | c.996A>T (p.Gly332=) c.963A>T (p.Gly321=) c.1008A>T (p.Gly336=) c.1020A>T (p.Gly340=) n.1202A>T c.1221A>T (p.Gly407=) c.1107A>T (p.Gly369=) | |
2 | g.136114920T>C | CA1890054 | CXCR4 | c.996A>G (p.Gly332=) c.963A>G (p.Gly321=) c.1008A>G (p.Gly336=) c.1020A>G (p.Gly340=) n.1202A>G c.1221A>G (p.Gly407=) c.1107A>G (p.Gly369=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
2 | g.136114920T>G | CA429191818 | CXCR4 | c.996A>C (p.Gly332=) c.963A>C (p.Gly321=) c.1008A>C (p.Gly336=) c.1020A>C (p.Gly340=) n.1202A>C c.1221A>C (p.Gly407=) c.1107A>C (p.Gly369=) | gnomAD v4 |
2 | g.136114920T= | CA1290965878 | CXCR4 | c.996A= (p.Gly332=) c.963A= (p.Gly321=) c.1008A= (p.Gly336=) c.1020A= (p.Gly340=) n.1202A= c.1221A= (p.Gly407=) c.1107A= (p.Gly369=) | |
2 | g.136114921C>A | CA348657437 | CXCR4 | c.995G>T (p.Gly332Val) c.962G>T (p.Gly321Val) c.1007G>T (p.Gly336Val) c.1019G>T (p.Gly340Val) n.1201G>T c.1220G>T (p.Gly407Val) c.1106G>T (p.Gly369Val) | |
2 | g.136114921C= | CA1290965879 | CXCR4 | c.995G= (p.Gly332=) c.962G= (p.Gly321=) c.1007G= (p.Gly336=) c.1019G= (p.Gly340=) n.1201G= c.1220G= (p.Gly407=) c.1106G= (p.Gly369=) | |
2 | g.136114921C>G | CA348657440 | CXCR4 | c.995G>C (p.Gly332Ala) c.962G>C (p.Gly321Ala) c.1007G>C (p.Gly336Ala) c.1019G>C (p.Gly340Ala) n.1201G>C c.1220G>C (p.Gly407Ala) c.1106G>C (p.Gly369Ala) | |
2 | g.136114921C>T | CA348657441 | CXCR4 | c.995G>A (p.Gly332Glu) c.962G>A (p.Gly321Glu) c.1007G>A (p.Gly336Glu) c.1019G>A (p.Gly340Glu) n.1201G>A c.1220G>A (p.Gly407Glu) c.1106G>A (p.Gly369Glu) | dbSNP |
2 | g.136114922C>A | CA348657446 | CXCR4 | c.994G>T (p.Gly332Ter) c.961G>T (p.Gly321Ter) c.1006G>T (p.Gly336Ter) c.1018G>T (p.Gly340Ter) n.1200G>T c.1219G>T (p.Gly407Ter) c.1105G>T (p.Gly369Ter) | ClinVar dbSNP gnomAD v4 COSMIC |
2 | g.136114922C>G | CA348657448 | CXCR4 | c.994G>C (p.Gly332Arg) c.961G>C (p.Gly321Arg) c.1006G>C (p.Gly336Arg) c.1018G>C (p.Gly340Arg) n.1200G>C c.1219G>C (p.Gly407Arg) c.1105G>C (p.Gly369Arg) | |
2 | g.136114922C>T | CA348657444 | CXCR4 | c.994G>A (p.Gly332Arg) c.961G>A (p.Gly321Arg) c.1006G>A (p.Gly336Arg) c.1018G>A (p.Gly340Arg) n.1200G>A c.1219G>A (p.Gly407Arg) c.1105G>A (p.Gly369Arg) | dbSNP |
2 | g.136114923A>C | CA429191820 | CXCR4 | c.993T>G (p.Gly331=) c.960T>G (p.Gly320=) c.1005T>G (p.Gly335=) c.1017T>G (p.Gly339=) n.1199T>G c.1218T>G (p.Gly406=) c.1104T>G (p.Gly368=) | |
2 | g.136114923A>G | CA429191821 | CXCR4 | c.993T>C (p.Gly331=) c.960T>C (p.Gly320=) c.1005T>C (p.Gly335=) c.1017T>C (p.Gly339=) n.1199T>C c.1218T>C (p.Gly406=) c.1104T>C (p.Gly368=) | |
2 | g.136114923A>T | CA429191819 | CXCR4 | c.993T>A (p.Gly331=) c.960T>A (p.Gly320=) c.1005T>A (p.Gly335=) c.1017T>A (p.Gly339=) n.1199T>A c.1218T>A (p.Gly406=) c.1104T>A (p.Gly368=) | |
2 | g.136114923dup | CA645539215 | CXCR4 | c.993dup (p.Gly332TrpfsTer8) c.960dup (p.Gly321TrpfsTer8) c.1005dup (p.Gly336TrpfsTer8) c.1017dup (p.Gly340TrpfsTer8) n.1199dup c.1218dup (p.Gly407TrpfsTer8) c.1104dup (p.Gly369TrpfsTer8) | COSMIC |
2 | g.136114924C>A | CA348657450 | CXCR4 | c.992G>T (p.Gly331Val) c.959G>T (p.Gly320Val) c.1004G>T (p.Gly335Val) c.1016G>T (p.Gly339Val) n.1198G>T c.1217G>T (p.Gly406Val) c.1103G>T (p.Gly368Val) | |
2 | g.136114924C>G | CA348657452 | CXCR4 | c.992G>C (p.Gly331Ala) c.959G>C (p.Gly320Ala) c.1004G>C (p.Gly335Ala) c.1016G>C (p.Gly339Ala) n.1198G>C c.1217G>C (p.Gly406Ala) c.1103G>C (p.Gly368Ala) | |
2 | g.136114924C>T | CA348657454 | CXCR4 | c.992G>A (p.Gly331Asp) c.959G>A (p.Gly320Asp) c.1004G>A (p.Gly335Asp) c.1016G>A (p.Gly339Asp) n.1198G>A c.1217G>A (p.Gly406Asp) c.1103G>A (p.Gly368Asp) | dbSNP |
2 | g.136114925C>A | CA348657456 | CXCR4 | c.991G>T (p.Gly331Cys) c.958G>T (p.Gly320Cys) c.1003G>T (p.Gly335Cys) c.1015G>T (p.Gly339Cys) n.1197G>T c.1216G>T (p.Gly406Cys) c.1102G>T (p.Gly368Cys) | dbSNP |
2 | g.136114925C= | CA1290965880 | CXCR4 | c.991G= (p.Gly331=) c.958G= (p.Gly320=) c.1003G= (p.Gly335=) c.1015G= (p.Gly339=) n.1197G= c.1216G= (p.Gly406=) c.1102G= (p.Gly368=) | |
2 | g.136114925C>G | CA348657459 | CXCR4 | c.991G>C (p.Gly331Arg) c.958G>C (p.Gly320Arg) c.1003G>C (p.Gly335Arg) c.1015G>C (p.Gly339Arg) n.1197G>C c.1216G>C (p.Gly406Arg) c.1102G>C (p.Gly368Arg) | |
2 | g.136114925C>T | CA1890055 | CXCR4 | c.991G>A (p.Gly331Ser) c.958G>A (p.Gly320Ser) c.1003G>A (p.Gly335Ser) c.1015G>A (p.Gly339Ser) n.1197G>A c.1216G>A (p.Gly406Ser) c.1102G>A (p.Gly368Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.136114926T>A | CA429191823 | CXCR4 | c.990A>T (p.Arg330=) c.957A>T (p.Arg319=) c.1002A>T (p.Arg334=) c.1014A>T (p.Arg338=) n.1196A>T c.1215A>T (p.Arg405=) c.1101A>T (p.Arg367=) | |
2 | g.136114926T>C | CA429191824 | CXCR4 | c.990A>G (p.Arg330=) c.957A>G (p.Arg319=) c.1002A>G (p.Arg334=) c.1014A>G (p.Arg338=) n.1196A>G c.1215A>G (p.Arg405=) c.1101A>G (p.Arg367=) | |
2 | g.136114926T>G | CA429191825 | CXCR4 | c.990A>C (p.Arg330=) c.957A>C (p.Arg319=) c.1002A>C (p.Arg334=) c.1014A>C (p.Arg338=) n.1196A>C c.1215A>C (p.Arg405=) c.1101A>C (p.Arg367=) | |
2 | g.136114927C>A | CA348657463 | CXCR4 | c.989G>T (p.Arg330Leu) c.956G>T (p.Arg319Leu) c.1001G>T (p.Arg334Leu) c.1013G>T (p.Arg338Leu) n.1195G>T c.1214G>T (p.Arg405Leu) c.1100G>T (p.Arg367Leu) |