Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.136114879_136114943delCA891841793CXCR4c.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)
2g.136114900_136115041dupCA2573133307CXCR4c.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
2g.136114916_136114919dupCA2573051654CXCR4c.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
2g.136114916_136114919delCA645539211CXCR4c.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
2g.136114915G>ACA348657409CXCR4c.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)
2g.136114915G>CCA123717CXCR4c.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
2g.136114915G=CA1290965875CXCR4c.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=)
2g.136114915G>TCA348657412CXCR4c.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
2g.136114916A>CCA348657414CXCR4c.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)
2g.136114916A>GCA348657416CXCR4c.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)
2g.136114916A>TCA348657417CXCR4c.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)
2g.136114917dupCA645539213CXCR4c.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
2g.136114917delCA645539214CXCR4c.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
2g.136114917A=CA1290965876CXCR4c.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=)
2g.136114917A>CCA348657419CXCR4c.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)
2g.136114917A>GCA429191813CXCR4c.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
2g.136114917A>TCA348657421CXCR4c.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)
2g.136114918T>ACA348657424CXCR4c.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)
2g.136114918T>CCA1890053CXCR4c.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
2g.136114918T>GCA348657426CXCR4c.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)
2g.136114918T=CA1290965877CXCR4c.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=)
2g.136114919G>ACA348657429CXCR4c.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)
2g.136114919G>CCA348657431CXCR4c.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)
2g.136114919G>TCA348657433CXCR4c.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)
2g.136114920T>ACA429191817CXCR4c.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=)
2g.136114920T>CCA1890054CXCR4c.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
2g.136114920T>GCA429191818CXCR4c.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
2g.136114920T=CA1290965878CXCR4c.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=)
2g.136114921C>ACA348657437CXCR4c.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)
2g.136114921C=CA1290965879CXCR4c.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=)
2g.136114921C>GCA348657440CXCR4c.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)
2g.136114921C>TCA348657441CXCR4c.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
2g.136114922C>ACA348657446CXCR4c.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
2g.136114922C>GCA348657448CXCR4c.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)
2g.136114922C>TCA348657444CXCR4c.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
2g.136114923A>CCA429191820CXCR4c.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=)
2g.136114923A>GCA429191821CXCR4c.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=)
2g.136114923A>TCA429191819CXCR4c.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=)
2g.136114923dupCA645539215CXCR4c.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
2g.136114924C>ACA348657450CXCR4c.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)
2g.136114924C>GCA348657452CXCR4c.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)
2g.136114924C>TCA348657454CXCR4c.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
2g.136114925C>ACA348657456CXCR4c.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
2g.136114925C=CA1290965880CXCR4c.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=)
2g.136114925C>GCA348657459CXCR4c.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)
2g.136114925C>TCA1890055CXCR4c.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
2g.136114926T>ACA429191823CXCR4c.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=)
2g.136114926T>CCA429191824CXCR4c.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=)
2g.136114926T>GCA429191825CXCR4c.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=)
2g.136114927C>ACA348657463CXCR4c.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)

Number of alleles fetched