Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.77933411G>A | CA340877032 | NEXN | c.1183G>A (p.Glu395Lys) c.991G>A (p.Glu331Lys) c.882G>A c.1141G>A (p.Glu381Lys) n.643G>A n.757G>A c.949G>A (p.Glu317Lys) c.766G>A (p.Glu256Lys) | |
1 | g.77933411G>C | CA340877030 | NEXN | c.1183G>C (p.Glu395Gln) c.991G>C (p.Glu331Gln) c.882G>C c.1141G>C (p.Glu381Gln) n.643G>C n.757G>C c.949G>C (p.Glu317Gln) c.766G>C (p.Glu256Gln) | |
1 | g.77933411G>T | CA340877031 | NEXN | c.1183G>T (p.Glu395Ter) c.991G>T (p.Glu331Ter) c.882G>T c.1141G>T (p.Glu381Ter) n.643G>T n.757G>T c.949G>T (p.Glu317Ter) c.766G>T (p.Glu256Ter) | |
1 | g.77933412A>C | CA340877034 | NEXN | c.1184A>C (p.Glu395Ala) c.992A>C (p.Glu331Ala) c.883A>C c.1142A>C (p.Glu381Ala) n.644A>C n.758A>C c.950A>C (p.Glu317Ala) c.767A>C (p.Glu256Ala) | |
1 | g.77933412A>G | CA340877036 | NEXN | c.1184A>G (p.Glu395Gly) c.992A>G (p.Glu331Gly) c.883A>G c.1142A>G (p.Glu381Gly) n.644A>G n.758A>G c.950A>G (p.Glu317Gly) c.767A>G (p.Glu256Gly) | |
1 | g.77933412A>T | CA340877037 | NEXN | c.1184A>T (p.Glu395Val) c.992A>T (p.Glu331Val) c.883A>T c.1142A>T (p.Glu381Val) n.644A>T n.758A>T c.950A>T (p.Glu317Val) c.767A>T (p.Glu256Val) | |
1 | g.77933413G>A | CA418572102 | NEXN | c.1185G>A (p.Glu395=) c.993G>A (p.Glu331=) c.884G>A c.1143G>A (p.Glu381=) n.645G>A n.759G>A c.951G>A (p.Glu317=) c.768G>A (p.Glu256=) | dbSNP |
1 | g.77933413G>C | CA340877039 | NEXN | c.1185G>C (p.Glu395Asp) c.993G>C (p.Glu331Asp) c.884G>C c.1143G>C (p.Glu381Asp) n.645G>C n.759G>C c.951G>C (p.Glu317Asp) c.768G>C (p.Glu256Asp) | |
1 | g.77933413G= | CA1177626750 | NEXN | c.1185G= (p.Glu395=) c.993G= (p.Glu331=) c.884G= c.1143G= (p.Glu381=) n.645G= n.759G= c.951G= (p.Glu317=) c.768G= (p.Glu256=) | |
1 | g.77933413G>T | CA918813 | NEXN | c.1185G>T (p.Glu395Asp) c.993G>T (p.Glu331Asp) c.884G>T c.1143G>T (p.Glu381Asp) n.645G>T n.759G>T c.951G>T (p.Glu317Asp) c.768G>T (p.Glu256Asp) | dbSNP ExAC gnomAD v2 |
1 | g.77933414G>A | CA918814 | NEXN | c.1186G>A (p.Glu396Lys) c.994G>A (p.Glu332Lys) c.885G>A c.1144G>A (p.Glu382Lys) n.646G>A n.760G>A c.952G>A (p.Glu318Lys) c.769G>A (p.Glu257Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933414G>C | CA340877042 | NEXN | c.1186G>C (p.Glu396Gln) c.994G>C (p.Glu332Gln) c.885G>C c.1144G>C (p.Glu382Gln) n.646G>C n.760G>C c.952G>C (p.Glu318Gln) c.769G>C (p.Glu257Gln) | |
1 | g.77933414G= | CA1145357745 | NEXN | c.1186G= (p.Glu396=) c.994G= (p.Glu332=) c.885G= c.1144G= (p.Glu382=) n.646G= n.760G= c.952G= (p.Glu318=) c.769G= (p.Glu257=) | |
1 | g.77933414G>T | CA340877043 | NEXN | c.1186G>T (p.Glu396Ter) c.994G>T (p.Glu332Ter) c.885G>T c.1144G>T (p.Glu382Ter) n.646G>T n.760G>T c.952G>T (p.Glu318Ter) c.769G>T (p.Glu257Ter) | gnomAD v4 |
1 | g.77933415A>C | CA340877045 | NEXN | c.1187A>C (p.Glu396Ala) c.995A>C (p.Glu332Ala) c.886A>C c.1145A>C (p.Glu382Ala) n.647A>C n.761A>C c.953A>C (p.Glu318Ala) c.770A>C (p.Glu257Ala) | |
1 | g.77933415A>G | CA340877046 | NEXN | c.1187A>G (p.Glu396Gly) c.995A>G (p.Glu332Gly) c.886A>G c.1145A>G (p.Glu382Gly) n.647A>G n.761A>G c.953A>G (p.Glu318Gly) c.770A>G (p.Glu257Gly) | |
1 | g.77933415A>T | CA340877047 | NEXN | c.1187A>T (p.Glu396Val) c.995A>T (p.Glu332Val) c.886A>T c.1145A>T (p.Glu382Val) n.647A>T n.761A>T c.953A>T (p.Glu318Val) c.770A>T (p.Glu257Val) | |
1 | g.77933416A>C | CA340877049 | NEXN | c.1188A>C (p.Glu396Asp) c.996A>C (p.Glu332Asp) c.887A>C c.1146A>C (p.Glu382Asp) n.648A>C n.762A>C c.954A>C (p.Glu318Asp) c.771A>C (p.Glu257Asp) | |
1 | g.77933416A>G | CA418572103 | NEXN | c.1188A>G (p.Glu396=) c.996A>G (p.Glu332=) c.887A>G c.1146A>G (p.Glu382=) n.648A>G n.762A>G c.954A>G (p.Glu318=) c.771A>G (p.Glu257=) | |
1 | g.77933416A>T | CA340877051 | NEXN | c.1188A>T (p.Glu396Asp) c.996A>T (p.Glu332Asp) c.887A>T c.1146A>T (p.Glu382Asp) n.648A>T n.762A>T c.954A>T (p.Glu318Asp) c.771A>T (p.Glu257Asp) | |
1 | g.77933417C>A | CA418572104 | NEXN | c.1189C>A (p.Arg397=) c.997C>A (p.Arg333=) c.888C>A c.1147C>A (p.Arg383=) n.649C>A n.763C>A c.955C>A (p.Arg319=) c.772C>A (p.Arg258=) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.77933417C= | CA1177626752 | NEXN | c.1189C= (p.Arg397=) c.997C= (p.Arg333=) c.888C= c.1147C= (p.Arg383=) n.649C= n.763C= c.955C= (p.Arg319=) c.772C= (p.Arg258=) | |
1 | g.77933417C>G | CA340877053 | NEXN | c.1189C>G (p.Arg397Gly) c.997C>G (p.Arg333Gly) c.888C>G c.1147C>G (p.Arg383Gly) n.649C>G n.763C>G c.955C>G (p.Arg319Gly) c.772C>G (p.Arg258Gly) | |
1 | g.77933417C>T | CA918815 | NEXN | c.1189C>T (p.Arg397Trp) c.997C>T (p.Arg333Trp) c.888C>T c.1147C>T (p.Arg383Trp) n.649C>T n.763C>T c.955C>T (p.Arg319Trp) c.772C>T (p.Arg258Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
1 | g.77933417_77933418delinsCG | CA1177626755 | NEXN | c.1189_1190delinsCG (p.Arg397=) c.997_998delinsCG (p.Arg333=) c.888_889delinsCG c.1147_1148delinsCG (p.Arg383=) n.649_650delinsCG n.763_764delinsCG c.955_956delinsCG (p.Arg319=) c.772_773delinsCG (p.Arg258=) | |
1 | g.77933418G>A | CA918816 | NEXN | c.1190G>A (p.Arg397Gln) c.998G>A (p.Arg333Gln) c.889G>A c.1148G>A (p.Arg383Gln) n.650G>A n.764G>A c.956G>A (p.Arg319Gln) c.773G>A (p.Arg258Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933418G>C | CA340877056 | NEXN | c.1190G>C (p.Arg397Pro) c.998G>C (p.Arg333Pro) c.889G>C c.1148G>C (p.Arg383Pro) n.650G>C n.764G>C c.956G>C (p.Arg319Pro) c.773G>C (p.Arg258Pro) | |
1 | g.77933418G= | CA1143506653 | NEXN | c.1190G= (p.Arg397=) c.998G= (p.Arg333=) c.889G= c.1148G= (p.Arg383=) n.650G= n.764G= c.956G= (p.Arg319=) c.773G= (p.Arg258=) | |
1 | g.77933418G>T | CA340877057 | NEXN | c.1190G>T (p.Arg397Leu) c.998G>T (p.Arg333Leu) c.889G>T c.1148G>T (p.Arg383Leu) n.650G>T n.764G>T c.956G>T (p.Arg319Leu) c.773G>T (p.Arg258Leu) | |
1 | g.77933418_77933419del | CA2600639591 | NEXN | c.1190_1191del (p.Arg397GlnfsTer3) c.998_999del (p.Arg333GlnfsTer3) c.889_890del c.1148_1149del (p.Arg383GlnfsTer3) n.650_651del n.764_765del c.956_957del (p.Arg319GlnfsTer3) c.773_774del (p.Arg258GlnfsTer3) | gnomAD v3 gnomAD v4 |
1 | g.77933419del | CA1177626756 | NEXN | c.1191del (p.Lys398SerfsTer4) c.999del (p.Lys334SerfsTer4) c.890del c.1149del (p.Lys384SerfsTer4) n.651del n.765del c.957del (p.Lys320SerfsTer4) c.774del (p.Lys259SerfsTer4) | dbSNP gnomAD v4 |
1 | g.77933419G>A | CA418572105 | NEXN | c.1191G>A (p.Arg397=) c.999G>A (p.Arg333=) c.890G>A c.1149G>A (p.Arg383=) n.651G>A n.765G>A c.957G>A (p.Arg319=) c.774G>A (p.Arg258=) | |
1 | g.77933419G>C | CA418572106 | NEXN | c.1191G>C (p.Arg397=) c.999G>C (p.Arg333=) c.890G>C c.1149G>C (p.Arg383=) n.651G>C n.765G>C c.957G>C (p.Arg319=) c.774G>C (p.Arg258=) | |
1 | g.77933419G>T | CA418572107 | NEXN | c.1191G>T (p.Arg397=) c.999G>T (p.Arg333=) c.890G>T c.1149G>T (p.Arg383=) n.651G>T n.765G>T c.957G>T (p.Arg319=) c.774G>T (p.Arg258=) | |
1 | g.77933420A>C | CA340877058 | NEXN | c.1192A>C (p.Lys398Gln) c.1000A>C (p.Lys334Gln) c.891A>C c.1150A>C (p.Lys384Gln) n.652A>C n.766A>C c.958A>C (p.Lys320Gln) c.775A>C (p.Lys259Gln) | ClinVar dbSNP |
1 | g.77933420A>G | CA340877060 | NEXN | c.1192A>G (p.Lys398Glu) c.1000A>G (p.Lys334Glu) c.891A>G c.1150A>G (p.Lys384Glu) n.652A>G n.766A>G c.958A>G (p.Lys320Glu) c.775A>G (p.Lys259Glu) | |
1 | g.77933420A>T | CA340877062 | NEXN | c.1192A>T (p.Lys398Ter) c.1000A>T (p.Lys334Ter) c.891A>T c.1150A>T (p.Lys384Ter) n.652A>T n.766A>T c.958A>T (p.Lys320Ter) c.775A>T (p.Lys259Ter) | |
1 | g.77933420_77933421insC | CA2600639592 | NEXN | c.1192_1193insC (p.Lys398ThrfsTer3) c.1000_1001insC (p.Lys334ThrfsTer3) c.891_892insC c.1150_1151insC (p.Lys384ThrfsTer3) n.652_653insC n.766_767insC c.958_959insC (p.Lys320ThrfsTer3) c.775_776insC (p.Lys259ThrfsTer3) | gnomAD v3 gnomAD v4 |
1 | g.77933421A= | CA1177626757 | NEXN | c.1193A= (p.Lys398=) c.1001A= (p.Lys334=) c.892A= c.1151A= (p.Lys384=) n.653A= n.767A= c.959A= (p.Lys320=) c.776A= (p.Lys259=) | |
1 | g.77933421A>C | CA340877063 | NEXN | c.1193A>C (p.Lys398Thr) c.1001A>C (p.Lys334Thr) c.892A>C c.1151A>C (p.Lys384Thr) n.653A>C n.767A>C c.959A>C (p.Lys320Thr) c.776A>C (p.Lys259Thr) | COSMIC COSMIC |
1 | g.77933421A>G | CA340877065 | NEXN | c.1193A>G (p.Lys398Arg) c.1001A>G (p.Lys334Arg) c.892A>G c.1151A>G (p.Lys384Arg) n.653A>G n.767A>G c.959A>G (p.Lys320Arg) c.776A>G (p.Lys259Arg) | dbSNP |
1 | g.77933421A>T | CA340877066 | NEXN | c.1193A>T (p.Lys398Met) c.1001A>T (p.Lys334Met) c.892A>T c.1151A>T (p.Lys384Met) n.653A>T n.767A>T c.959A>T (p.Lys320Met) c.776A>T (p.Lys259Met) | |
1 | g.77933422G>A | CA418572108 | NEXN | c.1194G>A (p.Lys398=) c.1002G>A (p.Lys334=) c.893G>A c.1152G>A (p.Lys384=) n.654G>A n.768G>A c.960G>A (p.Lys320=) c.777G>A (p.Lys259=) | |
1 | g.77933422G>C | CA340877070 | NEXN | c.1194G>C (p.Lys398Asn) c.1002G>C (p.Lys334Asn) c.893G>C c.1152G>C (p.Lys384Asn) n.654G>C n.768G>C c.960G>C (p.Lys320Asn) c.777G>C (p.Lys259Asn) | |
1 | g.77933422G>T | CA340877068 | NEXN | c.1194G>T (p.Lys398Asn) c.1002G>T (p.Lys334Asn) c.893G>T c.1152G>T (p.Lys384Asn) n.654G>T n.768G>T c.960G>T (p.Lys320Asn) c.777G>T (p.Lys259Asn) | |
1 | g.77933423C>A | CA918817 | NEXN | c.1195C>A (p.His399Asn) c.1003C>A (p.His335Asn) c.894C>A c.1153C>A (p.His385Asn) n.655C>A n.769C>A c.961C>A (p.His321Asn) c.778C>A (p.His260Asn) | ClinVar dbSNP ExAC gnomAD v2 |
1 | g.77933423C= | CA1177626758 | NEXN | c.1195C= (p.His399=) c.1003C= (p.His335=) c.894C= c.1153C= (p.His385=) n.655C= n.769C= c.961C= (p.His321=) c.778C= (p.His260=) | |
1 | g.77933423C>G | CA340877072 | NEXN | c.1195C>G (p.His399Asp) c.1003C>G (p.His335Asp) c.894C>G c.1153C>G (p.His385Asp) n.655C>G n.769C>G c.961C>G (p.His321Asp) c.778C>G (p.His260Asp) | |
1 | g.77933423C>T | CA340877073 | NEXN | c.1195C>T (p.His399Tyr) c.1003C>T (p.His335Tyr) c.894C>T c.1153C>T (p.His385Tyr) n.655C>T n.769C>T c.961C>T (p.His321Tyr) c.778C>T (p.His260Tyr) | |
1 | g.77933424A= | CA1177626759 | NEXN | c.1196A= (p.His399=) c.1004A= (p.His335=) c.895A= c.1154A= (p.His385=) n.656A= n.770A= c.962A= (p.His321=) c.779A= (p.His260=) | |
1 | g.77933424A>C | CA340877076 | NEXN | c.1196A>C (p.His399Pro) c.1004A>C (p.His335Pro) c.895A>C c.1154A>C (p.His385Pro) n.656A>C n.770A>C c.962A>C (p.His321Pro) c.779A>C (p.His260Pro) | |
1 | g.77933424A>G | CA340877077 | NEXN | c.1196A>G (p.His399Arg) c.1004A>G (p.His335Arg) c.895A>G c.1154A>G (p.His385Arg) n.656A>G n.770A>G c.962A>G (p.His321Arg) c.779A>G (p.His260Arg) | dbSNP gnomAD v4 |
1 | g.77933424A>T | CA340877078 | NEXN | c.1196A>T (p.His399Leu) c.1004A>T (p.His335Leu) c.895A>T c.1154A>T (p.His385Leu) n.656A>T n.770A>T c.962A>T (p.His321Leu) c.779A>T (p.His260Leu) | |
1 | g.77933425T>A | CA340877080 | NEXN | c.1197T>A (p.His399Gln) c.1005T>A (p.His335Gln) c.896T>A c.1155T>A (p.His385Gln) n.657T>A n.771T>A c.963T>A (p.His321Gln) c.780T>A (p.His260Gln) | dbSNP |
1 | g.77933425T>C | CA418572109 | NEXN | c.1197T>C (p.His399=) c.1005T>C (p.His335=) c.896T>C c.1155T>C (p.His385=) n.657T>C n.771T>C c.963T>C (p.His321=) c.780T>C (p.His260=) | |
1 | g.77933425T>G | CA340877082 | NEXN | c.1197T>G (p.His399Gln) c.1005T>G (p.His335Gln) c.896T>G c.1155T>G (p.His385Gln) n.657T>G n.771T>G c.963T>G (p.His321Gln) c.780T>G (p.His260Gln) | |
1 | g.77933425T= | CA1177626760 | NEXN | c.1197T= (p.His399=) c.1005T= (p.His335=) c.896T= c.1155T= (p.His385=) n.657T= n.771T= c.963T= (p.His321=) c.780T= (p.His260=) | |
1 | g.77933426A>C | CA340877083 | NEXN | c.1198A>C (p.Lys400Gln) c.1006A>C (p.Lys336Gln) c.897A>C c.1156A>C (p.Lys386Gln) n.658A>C n.772A>C c.964A>C (p.Lys322Gln) c.781A>C (p.Lys261Gln) | |
1 | g.77933426A>G | CA340877085 | NEXN | c.1198A>G (p.Lys400Glu) c.1006A>G (p.Lys336Glu) c.897A>G c.1156A>G (p.Lys386Glu) n.658A>G n.772A>G c.964A>G (p.Lys322Glu) c.781A>G (p.Lys261Glu) | gnomAD v4 |
1 | g.77933426A>T | CA340877086 | NEXN | c.1198A>T (p.Lys400Ter) c.1006A>T (p.Lys336Ter) c.897A>T c.1156A>T (p.Lys386Ter) n.658A>T n.772A>T c.964A>T (p.Lys322Ter) c.781A>T (p.Lys261Ter) | |
1 | g.77933427A= | CA1177626761 | NEXN | c.1199A= (p.Lys400=) c.1007A= (p.Lys336=) c.898A= c.1157A= (p.Lys386=) n.659A= n.773A= c.965A= (p.Lys322=) c.782A= (p.Lys261=) | |
1 | g.77933427A>C | CA340877087 | NEXN | c.1199A>C (p.Lys400Thr) c.1007A>C (p.Lys336Thr) c.898A>C c.1157A>C (p.Lys386Thr) n.659A>C n.773A>C c.965A>C (p.Lys322Thr) c.782A>C (p.Lys261Thr) | dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
1 | g.77933427A>G | CA24684308 | NEXN | c.1199A>G (p.Lys400Arg) c.1007A>G (p.Lys336Arg) c.898A>G c.1157A>G (p.Lys386Arg) n.659A>G n.773A>G c.965A>G (p.Lys322Arg) c.782A>G (p.Lys261Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933427A>T | CA340877090 | NEXN | c.1199A>T (p.Lys400Met) c.1007A>T (p.Lys336Met) c.898A>T c.1157A>T (p.Lys386Met) n.659A>T n.773A>T c.965A>T (p.Lys322Met) c.782A>T (p.Lys261Met) | |
1 | g.77933428G>A | CA418572110 | NEXN | c.1200G>A (p.Lys400=) c.1008G>A (p.Lys336=) c.899G>A c.1158G>A (p.Lys386=) n.660G>A n.774G>A c.966G>A (p.Lys322=) c.783G>A (p.Lys261=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.77933428G>C | CA918818 | NEXN | c.1200G>C (p.Lys400Asn) c.1008G>C (p.Lys336Asn) c.899G>C c.1158G>C (p.Lys386Asn) n.660G>C n.774G>C c.966G>C (p.Lys322Asn) c.783G>C (p.Lys261Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.77933428G= | CA1177626763 | NEXN | c.1200G= (p.Lys400=) c.1008G= (p.Lys336=) c.899G= c.1158G= (p.Lys386=) n.660G= n.774G= c.966G= (p.Lys322=) c.783G= (p.Lys261=) | |
1 | g.77933428G>T | CA340877092 | NEXN | c.1200G>T (p.Lys400Asn) c.1008G>T (p.Lys336Asn) c.899G>T c.1158G>T (p.Lys386Asn) n.660G>T n.774G>T c.966G>T (p.Lys322Asn) c.783G>T (p.Lys261Asn) | |
1 | g.77933429C>A | CA340877093 | NEXN | c.1201C>A (p.Leu401Ile) c.1009C>A (p.Leu337Ile) c.900C>A c.1159C>A (p.Leu387Ile) n.661C>A n.775C>A c.967C>A (p.Leu323Ile) c.784C>A (p.Leu262Ile) | |
1 | g.77933429C>G | CA340877095 | NEXN | c.1201C>G (p.Leu401Val) c.1009C>G (p.Leu337Val) c.900C>G c.1159C>G (p.Leu387Val) n.661C>G n.775C>G c.967C>G (p.Leu323Val) c.784C>G (p.Leu262Val) | ClinVar |
1 | g.77933429C>T | CA418572111 | NEXN | c.1201C>T (p.Leu401=) c.1009C>T (p.Leu337=) c.900C>T c.1159C>T (p.Leu387=) n.661C>T n.775C>T c.967C>T (p.Leu323=) c.784C>T (p.Leu262=) | |
1 | g.77933430T>A | CA340877096 | NEXN | c.1202T>A (p.Leu401Gln) c.1010T>A (p.Leu337Gln) c.901T>A c.1160T>A (p.Leu387Gln) n.662T>A n.776T>A c.968T>A (p.Leu323Gln) c.785T>A (p.Leu262Gln) | |
1 | g.77933430T>C | CA340877097 | NEXN | c.1202T>C (p.Leu401Pro) c.1010T>C (p.Leu337Pro) c.901T>C c.1160T>C (p.Leu387Pro) n.662T>C n.776T>C c.968T>C (p.Leu323Pro) c.785T>C (p.Leu262Pro) | ClinVar |
1 | g.77933430T>G | CA340877099 | NEXN | c.1202T>G (p.Leu401Arg) c.1010T>G (p.Leu337Arg) c.901T>G c.1160T>G (p.Leu387Arg) n.662T>G n.776T>G c.968T>G (p.Leu323Arg) c.785T>G (p.Leu262Arg) | |
1 | g.77933430_77933431insGGTTA | CA2744232065 | NEXN | c.1202_1203insGGTTA (p.Glu402ValfsTer12) c.1010_1011insGGTTA (p.Glu338ValfsTer12) c.901_902insGGTTA c.1160_1161insGGTTA (p.Glu388ValfsTer12) n.662_663insGGTTA n.776_777insGGTTA c.968_969insGGTTA (p.Glu324ValfsTer12) c.785_786insGGTTA (p.Glu263ValfsTer12) | |
1 | g.77933431A= | CA1177626764 | NEXN | c.1203A= (p.Leu401=) c.1011A= (p.Leu337=) c.902A= c.1161A= (p.Leu387=) n.663A= n.777A= c.969A= (p.Leu323=) c.786A= (p.Leu262=) | |
1 | g.77933431A>C | CA418572113 | NEXN | c.1203A>C (p.Leu401=) c.1011A>C (p.Leu337=) c.902A>C c.1161A>C (p.Leu387=) n.663A>C n.777A>C c.969A>C (p.Leu323=) c.786A>C (p.Leu262=) | |
1 | g.77933431A>G | CA918819 | NEXN | c.1203A>G (p.Leu401=) c.1011A>G (p.Leu337=) c.902A>G c.1161A>G (p.Leu387=) n.663A>G n.777A>G c.969A>G (p.Leu323=) c.786A>G (p.Leu262=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.77933431A>T | CA418572112 | NEXN | c.1203A>T (p.Leu401=) c.1011A>T (p.Leu337=) c.902A>T c.1161A>T (p.Leu387=) n.663A>T n.777A>T c.969A>T (p.Leu323=) c.786A>T (p.Leu262=) | |
1 | g.77933432G>A | CA340877102 | NEXN | c.1204G>A (p.Glu402Lys) c.1012G>A (p.Glu338Lys) c.903G>A c.1162G>A (p.Glu388Lys) n.664G>A n.778G>A c.970G>A (p.Glu324Lys) c.787G>A (p.Glu263Lys) | COSMIC |
1 | g.77933432G>C | CA340877104 | NEXN | c.1204G>C (p.Glu402Gln) c.1012G>C (p.Glu338Gln) c.903G>C c.1162G>C (p.Glu388Gln) n.664G>C n.778G>C c.970G>C (p.Glu324Gln) c.787G>C (p.Glu263Gln) | |
1 | g.77933432G>T | CA340877105 | NEXN | c.1204G>T (p.Glu402Ter) c.1012G>T (p.Glu338Ter) c.903G>T c.1162G>T (p.Glu388Ter) n.664G>T n.778G>T c.970G>T (p.Glu324Ter) c.787G>T (p.Glu263Ter) | |
1 | g.77933433A>C | CA340877107 | NEXN | c.1205A>C (p.Glu402Ala) c.1013A>C (p.Glu338Ala) c.904A>C c.1163A>C (p.Glu388Ala) n.665A>C n.779A>C c.971A>C (p.Glu324Ala) c.788A>C (p.Glu263Ala) | |
1 | g.77933433A>G | CA340877109 | NEXN | c.1205A>G (p.Glu402Gly) c.1013A>G (p.Glu338Gly) c.904A>G c.1163A>G (p.Glu388Gly) n.665A>G n.779A>G c.971A>G (p.Glu324Gly) c.788A>G (p.Glu263Gly) | |
1 | g.77933433A>T | CA340877110 | NEXN | c.1205A>T (p.Glu402Val) c.1013A>T (p.Glu338Val) c.904A>T c.1163A>T (p.Glu388Val) n.665A>T n.779A>T c.971A>T (p.Glu324Val) c.788A>T (p.Glu263Val) | |
1 | g.77933434A= | CA1177626765 | NEXN | c.1206A= (p.Glu402=) c.1014A= (p.Glu338=) c.905A= c.1164A= (p.Glu388=) n.666A= n.780A= c.972A= (p.Glu324=) c.789A= (p.Glu263=) | |
1 | g.77933434A>C | CA340877112 | NEXN | c.1206A>C (p.Glu402Asp) c.1014A>C (p.Glu338Asp) c.905A>C c.1164A>C (p.Glu388Asp) n.666A>C n.780A>C c.972A>C (p.Glu324Asp) c.789A>C (p.Glu263Asp) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.77933434A>G | CA418572114 | NEXN | c.1206A>G (p.Glu402=) c.1014A>G (p.Glu338=) c.905A>G c.1164A>G (p.Glu388=) n.666A>G n.780A>G c.972A>G (p.Glu324=) c.789A>G (p.Glu263=) | |
1 | g.77933434A>T | CA340877113 | NEXN | c.1206A>T (p.Glu402Asp) c.1014A>T (p.Glu338Asp) c.905A>T c.1164A>T (p.Glu388Asp) n.666A>T n.780A>T c.972A>T (p.Glu324Asp) c.789A>T (p.Glu263Asp) | |
1 | g.77933435_77933439dup | CA2574414091 | NEXN | c.1207_1211dup (p.Lys405TrpfsTer9) c.1015_1019dup (p.Lys341TrpfsTer9) c.906_910dup c.1165_1169dup (p.Lys391TrpfsTer9) n.667_671dup n.781_785dup c.973_977dup (p.Lys327TrpfsTer9) c.790_794dup (p.Lys266TrpfsTer9) | |
1 | g.77933435A>C | CA340877115 | NEXN | c.1207A>C (p.Met403Leu) c.1015A>C (p.Met339Leu) c.906A>C c.1165A>C (p.Met389Leu) n.667A>C n.781A>C c.973A>C (p.Met325Leu) c.790A>C (p.Met264Leu) | |
1 | g.77933435A>G | CA340877117 | NEXN | c.1207A>G (p.Met403Val) c.1015A>G (p.Met339Val) c.906A>G c.1165A>G (p.Met389Val) n.667A>G n.781A>G c.973A>G (p.Met325Val) c.790A>G (p.Met264Val) | |
1 | g.77933435A>T | CA340877118 | NEXN | c.1207A>T (p.Met403Leu) c.1015A>T (p.Met339Leu) c.906A>T c.1165A>T (p.Met389Leu) n.667A>T n.781A>T c.973A>T (p.Met325Leu) c.790A>T (p.Met264Leu) | |
1 | g.77933436T>A | CA340877120 | NEXN | c.1208T>A (p.Met403Lys) c.1016T>A (p.Met339Lys) c.907T>A c.1166T>A (p.Met389Lys) n.668T>A n.782T>A c.974T>A (p.Met325Lys) c.791T>A (p.Met264Lys) | |
1 | g.77933436T>C | CA340877122 | NEXN | c.1208T>C (p.Met403Thr) c.1016T>C (p.Met339Thr) c.907T>C c.1166T>C (p.Met389Thr) n.668T>C n.782T>C c.974T>C (p.Met325Thr) c.791T>C (p.Met264Thr) | |
1 | g.77933436T>G | CA340877124 | NEXN | c.1208T>G (p.Met403Arg) c.1016T>G (p.Met339Arg) c.907T>G c.1166T>G (p.Met389Arg) n.668T>G n.782T>G c.974T>G (p.Met325Arg) c.791T>G (p.Met264Arg) | |
1 | g.77933437G>A | CA340877125 | NEXN | c.1209G>A (p.Met403Ile) c.1017G>A (p.Met339Ile) c.908G>A c.1167G>A (p.Met389Ile) n.669G>A n.783G>A c.975G>A (p.Met325Ile) c.792G>A (p.Met264Ile) | |
1 | g.77933437G>C | CA340877126 | NEXN | c.1209G>C (p.Met403Ile) c.1017G>C (p.Met339Ile) c.908G>C c.1167G>C (p.Met389Ile) n.669G>C n.783G>C c.975G>C (p.Met325Ile) c.792G>C (p.Met264Ile) | |
1 | g.77933437G>T | CA340877128 | NEXN | c.1209G>T (p.Met403Ile) c.1017G>T (p.Met339Ile) c.908G>T c.1167G>T (p.Met389Ile) n.669G>T n.783G>T c.975G>T (p.Met325Ile) c.792G>T (p.Met264Ile) | |
1 | g.77933438G>A | CA340877130 | NEXN | c.1210G>A (p.Glu404Lys) c.1018G>A (p.Glu340Lys) c.909G>A c.1168G>A (p.Glu390Lys) n.670G>A n.784G>A c.976G>A (p.Glu326Lys) c.793G>A (p.Glu265Lys) | |
1 | g.77933438G>C | CA340877132 | NEXN | c.1210G>C (p.Glu404Gln) c.1018G>C (p.Glu340Gln) c.909G>C c.1168G>C (p.Glu390Gln) n.670G>C n.784G>C c.976G>C (p.Glu326Gln) c.793G>C (p.Glu265Gln) | gnomAD v4 |
1 | g.77933438G>T | CA340877133 | NEXN | c.1210G>T (p.Glu404Ter) c.1018G>T (p.Glu340Ter) c.909G>T c.1168G>T (p.Glu390Ter) n.670G>T n.784G>T c.976G>T (p.Glu326Ter) c.793G>T (p.Glu265Ter) | |
1 | g.77933438_77933445delinsGAGAAACA | CA1177626766 | NEXN | c.1210_1217delinsGAGAAACA (p.Glu404=) c.1018_1025delinsGAGAAACA (p.Glu340=) c.909_916delinsGAGAAACA c.1168_1175delinsGAGAAACA (p.Glu390=) n.670_677delinsGAGAAACA n.784_791delinsGAGAAACA c.976_983delinsGAGAAACA (p.Glu326=) c.793_800delinsGAGAAACA (p.Glu265=) | |
1 | g.77933439A>C | CA340877138 | NEXN | c.1211A>C (p.Glu404Ala) c.1019A>C (p.Glu340Ala) c.910A>C c.1169A>C (p.Glu390Ala) n.671A>C n.785A>C c.977A>C (p.Glu326Ala) c.794A>C (p.Glu265Ala) | |
1 | g.77933439A>G | CA340877137 | NEXN | c.1211A>G (p.Glu404Gly) c.1019A>G (p.Glu340Gly) c.910A>G c.1169A>G (p.Glu390Gly) n.671A>G n.785A>G c.977A>G (p.Glu326Gly) c.794A>G (p.Glu265Gly) | |
1 | g.77933439A>T | CA340877135 | NEXN | c.1211A>T (p.Glu404Val) c.1019A>T (p.Glu340Val) c.910A>T c.1169A>T (p.Glu390Val) n.671A>T n.785A>T c.977A>T (p.Glu326Val) c.794A>T (p.Glu265Val) | |
1 | g.77933443_77933449del | CA918820 | NEXN | c.1215_1221del (p.Lys405AsnfsTer5) c.1023_1029del (p.Lys341AsnfsTer5) c.914_920del c.1173_1179del (p.Lys391AsnfsTer5) n.675_681del n.789_795del c.981_987del (p.Lys327AsnfsTer5) c.798_804del (p.Lys266AsnfsTer5) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.77933440G>A | CA418572115 | NEXN | c.1212G>A (p.Glu404=) c.1020G>A (p.Glu340=) c.911G>A c.1170G>A (p.Glu390=) n.672G>A n.786G>A c.978G>A (p.Glu326=) c.795G>A (p.Glu265=) | |
1 | g.77933440G>C | CA340877140 | NEXN | c.1212G>C (p.Glu404Asp) c.1020G>C (p.Glu340Asp) c.911G>C c.1170G>C (p.Glu390Asp) n.672G>C n.786G>C c.978G>C (p.Glu326Asp) c.795G>C (p.Glu265Asp) | |
1 | g.77933440G>T | CA340877141 | NEXN | c.1212G>T (p.Glu404Asp) c.1020G>T (p.Glu340Asp) c.911G>T c.1170G>T (p.Glu390Asp) n.672G>T n.786G>T c.978G>T (p.Glu326Asp) c.795G>T (p.Glu265Asp) | |
1 | g.77933441A>C | CA340877143 | NEXN | c.1213A>C (p.Lys405Gln) c.1021A>C (p.Lys341Gln) c.912A>C c.1171A>C (p.Lys391Gln) n.673A>C n.787A>C c.979A>C (p.Lys327Gln) c.796A>C (p.Lys266Gln) | |
1 | g.77933441A>G | CA340877145 | NEXN | c.1213A>G (p.Lys405Glu) c.1021A>G (p.Lys341Glu) c.912A>G c.1171A>G (p.Lys391Glu) n.673A>G n.787A>G c.979A>G (p.Lys327Glu) c.796A>G (p.Lys266Glu) | |
1 | g.77933441A>T | CA340877146 | NEXN | c.1213A>T (p.Lys405Ter) c.1021A>T (p.Lys341Ter) c.912A>T c.1171A>T (p.Lys391Ter) n.673A>T n.787A>T c.979A>T (p.Lys327Ter) c.796A>T (p.Lys266Ter) | gnomAD v4 |
1 | g.77933442A>C | CA340877148 | NEXN | c.1214A>C (p.Lys405Thr) c.1022A>C (p.Lys341Thr) c.913A>C c.1172A>C (p.Lys391Thr) n.674A>C n.788A>C c.980A>C (p.Lys327Thr) c.797A>C (p.Lys266Thr) | |
1 | g.77933442A>G | CA340877150 | NEXN | c.1214A>G (p.Lys405Arg) c.1022A>G (p.Lys341Arg) c.913A>G c.1172A>G (p.Lys391Arg) n.674A>G n.788A>G c.980A>G (p.Lys327Arg) c.797A>G (p.Lys266Arg) | |
1 | g.77933442A>T | CA340877151 | NEXN | c.1214A>T (p.Lys405Ile) c.1022A>T (p.Lys341Ile) c.913A>T c.1172A>T (p.Lys391Ile) n.674A>T n.788A>T c.980A>T (p.Lys327Ile) c.797A>T (p.Lys266Ile) | |
1 | g.77933443A>C | CA340877153 | NEXN | c.1215A>C (p.Lys405Asn) c.1023A>C (p.Lys341Asn) c.914A>C c.1173A>C (p.Lys391Asn) n.675A>C n.789A>C c.981A>C (p.Lys327Asn) c.798A>C (p.Lys266Asn) | |
1 | g.77933443A>G | CA418572117 | NEXN | c.1215A>G (p.Lys405=) c.1023A>G (p.Lys341=) c.914A>G c.1173A>G (p.Lys391=) n.675A>G n.789A>G c.981A>G (p.Lys327=) c.798A>G (p.Lys266=) | |
1 | g.77933443A>T | CA340877154 | NEXN | c.1215A>T (p.Lys405Asn) c.1023A>T (p.Lys341Asn) c.914A>T c.1173A>T (p.Lys391Asn) n.675A>T n.789A>T c.981A>T (p.Lys327Asn) c.798A>T (p.Lys266Asn) | |
1 | g.77933444C>A | CA340877157 | NEXN | c.1216C>A (p.Gln406Lys) c.1024C>A (p.Gln342Lys) c.915C>A c.1174C>A (p.Gln392Lys) n.676C>A n.790C>A c.982C>A (p.Gln328Lys) c.799C>A (p.Gln267Lys) | |
1 | g.77933444C= | CA1177626769 | NEXN | c.1216C= (p.Gln406=) c.1024C= (p.Gln342=) c.915C= c.1174C= (p.Gln392=) n.676C= n.790C= c.982C= (p.Gln328=) c.799C= (p.Gln267=) | |
1 | g.77933444C>G | CA340877158 | NEXN | c.1216C>G (p.Gln406Glu) c.1024C>G (p.Gln342Glu) c.915C>G c.1174C>G (p.Gln392Glu) n.676C>G n.790C>G c.982C>G (p.Gln328Glu) c.799C>G (p.Gln267Glu) | |
1 | g.77933444C>T | CA340877159 | NEXN | c.1216C>T (p.Gln406Ter) c.1024C>T (p.Gln342Ter) c.915C>T c.1174C>T (p.Gln392Ter) n.676C>T n.790C>T c.982C>T (p.Gln328Ter) c.799C>T (p.Gln267Ter) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.77933444_77933447delinsCAAG | CA1177626768 | NEXN | c.1216_1219delinsCAAG (p.Gln406=) c.1024_1027delinsCAAG (p.Gln342=) c.915_918delinsCAAG c.1174_1177delinsCAAG (p.Gln392=) n.676_679delinsCAAG n.790_793delinsCAAG c.982_985delinsCAAG (p.Gln328=) c.799_802delinsCAAG (p.Gln267=) | |
1 | g.77933445A>C | CA340877162 | NEXN | c.1217A>C (p.Gln406Pro) c.1025A>C (p.Gln342Pro) c.916A>C c.1175A>C (p.Gln392Pro) n.677A>C n.791A>C c.983A>C (p.Gln328Pro) c.800A>C (p.Gln267Pro) | |
1 | g.77933445A>G | CA340877163 | NEXN | c.1217A>G (p.Gln406Arg) c.1025A>G (p.Gln342Arg) c.916A>G c.1175A>G (p.Gln392Arg) n.677A>G n.791A>G c.983A>G (p.Gln328Arg) c.800A>G (p.Gln267Arg) | gnomAD v4 |
1 | g.77933445A>T | CA340877164 | NEXN | c.1217A>T (p.Gln406Leu) c.1025A>T (p.Gln342Leu) c.916A>T c.1175A>T (p.Gln392Leu) n.677A>T n.791A>T c.983A>T (p.Gln328Leu) c.800A>T (p.Gln267Leu) | gnomAD v4 |
1 | g.77933447_77933449del | CA918821 | NEXN | c.1219_1221del (p.Glu407del) c.1027_1029del (p.Glu343del) c.918_920del c.1177_1179del (p.Glu393del) n.679_681del n.793_795del c.985_987del (p.Glu329del) c.802_804del (p.Glu268del) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933446A= | CA1177626772 | NEXN | c.1218A= (p.Gln406=) c.1026A= (p.Gln342=) c.917A= c.1176A= (p.Gln392=) n.678A= n.792A= c.984A= (p.Gln328=) c.801A= (p.Gln267=) | |
1 | g.77933446A>C | CA918822 | NEXN | c.1218A>C (p.Gln406His) c.1026A>C (p.Gln342His) c.917A>C c.1176A>C (p.Gln392His) n.678A>C n.792A>C c.984A>C (p.Gln328His) c.801A>C (p.Gln267His) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.77933446A>G | CA418572119 | NEXN | c.1218A>G (p.Gln406=) c.1026A>G (p.Gln342=) c.917A>G c.1176A>G (p.Gln392=) n.678A>G n.792A>G c.984A>G (p.Gln328=) c.801A>G (p.Gln267=) | dbSNP gnomAD v4 |
1 | g.77933446A>T | CA340877167 | NEXN | c.1218A>T (p.Gln406His) c.1026A>T (p.Gln342His) c.917A>T c.1176A>T (p.Gln392His) n.678A>T n.792A>T c.984A>T (p.Gln328His) c.801A>T (p.Gln267His) | |
1 | g.77933447G>A | CA340877169 | NEXN | c.1219G>A (p.Glu407Lys) c.1027G>A (p.Glu343Lys) c.918G>A c.1177G>A (p.Glu393Lys) n.679G>A n.793G>A c.985G>A (p.Glu329Lys) c.802G>A (p.Glu268Lys) | |
1 | g.77933447G>C | CA340877170 | NEXN | c.1219G>C (p.Glu407Gln) c.1027G>C (p.Glu343Gln) c.918G>C c.1177G>C (p.Glu393Gln) n.679G>C n.793G>C c.985G>C (p.Glu329Gln) c.802G>C (p.Glu268Gln) | |
1 | g.77933447G>T | CA340877172 | NEXN | c.1219G>T (p.Glu407Ter) c.1027G>T (p.Glu343Ter) c.918G>T c.1177G>T (p.Glu393Ter) n.679G>T n.793G>T c.985G>T (p.Glu329Ter) c.802G>T (p.Glu268Ter) | gnomAD v4 |
1 | g.77933448A>C | CA340877174 | NEXN | c.1220A>C (p.Glu407Ala) c.1028A>C (p.Glu343Ala) c.919A>C c.1178A>C (p.Glu393Ala) n.680A>C n.794A>C c.986A>C (p.Glu329Ala) c.803A>C (p.Glu268Ala) | |
1 | g.77933448A>G | CA340877176 | NEXN | c.1220A>G (p.Glu407Gly) c.1028A>G (p.Glu343Gly) c.919A>G c.1178A>G (p.Glu393Gly) n.680A>G n.794A>G c.986A>G (p.Glu329Gly) c.803A>G (p.Glu268Gly) | gnomAD v4 |
1 | g.77933448A>T | CA340877177 | NEXN | c.1220A>T (p.Glu407Val) c.1028A>T (p.Glu343Val) c.919A>T c.1178A>T (p.Glu393Val) n.680A>T n.794A>T c.986A>T (p.Glu329Val) c.803A>T (p.Glu268Val) | |
1 | g.77933449A>C | CA340877179 | NEXN | c.1221A>C (p.Glu407Asp) c.1029A>C (p.Glu343Asp) c.920A>C c.1179A>C (p.Glu393Asp) n.681A>C n.795A>C c.987A>C (p.Glu329Asp) c.804A>C (p.Glu268Asp) | |
1 | g.77933449A>G | CA418572120 | NEXN | c.1221A>G (p.Glu407=) c.1029A>G (p.Glu343=) c.920A>G c.1179A>G (p.Glu393=) n.681A>G n.795A>G c.987A>G (p.Glu329=) c.804A>G (p.Glu268=) | |
1 | g.77933449A>T | CA340877181 | NEXN | c.1221A>T (p.Glu407Asp) c.1029A>T (p.Glu343Asp) c.920A>T c.1179A>T (p.Glu393Asp) n.681A>T n.795A>T c.987A>T (p.Glu329Asp) c.804A>T (p.Glu268Asp) | |
1 | g.77933450T>A | CA340877184 | NEXN | c.1222T>A (p.Phe408Ile) c.1030T>A (p.Phe344Ile) c.921T>A c.1180T>A (p.Phe394Ile) n.682T>A n.796T>A c.988T>A (p.Phe330Ile) c.805T>A (p.Phe269Ile) | |
1 | g.77933450T>C | CA335409 | NEXN | c.1222T>C (p.Phe408Leu) c.1030T>C (p.Phe344Leu) c.921T>C c.1180T>C (p.Phe394Leu) n.682T>C n.796T>C c.988T>C (p.Phe330Leu) c.805T>C (p.Phe269Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933450T>G | CA340877183 | NEXN | c.1222T>G (p.Phe408Val) c.1030T>G (p.Phe344Val) c.921T>G c.1180T>G (p.Phe394Val) n.682T>G n.796T>G c.988T>G (p.Phe330Val) c.805T>G (p.Phe269Val) | |
1 | g.77933450T= | CA1177626774 | NEXN | c.1222T= (p.Phe408=) c.1030T= (p.Phe344=) c.921T= c.1180T= (p.Phe394=) n.682T= n.796T= c.988T= (p.Phe330=) c.805T= (p.Phe269=) | |
1 | g.77933452_77933453insCTTTTTTTT | CA2646274523 | NEXN | c.1224_1225insCTTTTTTTT (p.Phe408_Glu409insLeuPhePhe) c.1032_1033insCTTTTTTTT (p.Phe344_Glu345insLeuPhePhe) c.923_924insCTTTTTTTT c.1182_1183insCTTTTTTTT (p.Phe394_Glu395insLeuPhePhe) n.684_685insCTTTTTTTT n.798_799insCTTTTTTTT c.990_991insCTTTTTTTT (p.Phe330_Glu331insLeuPhePhe) c.807_808insCTTTTTTTT (p.Phe269_Glu270insLeuPhePhe) | gnomAD v4 |
1 | g.77933451T>A | CA340877187 | NEXN | c.1223T>A (p.Phe408Tyr) c.1031T>A (p.Phe344Tyr) c.922T>A c.1181T>A (p.Phe394Tyr) n.683T>A n.797T>A c.989T>A (p.Phe330Tyr) c.806T>A (p.Phe269Tyr) | |
1 | g.77933451T>C | CA340877188 | NEXN | c.1223T>C (p.Phe408Ser) c.1031T>C (p.Phe344Ser) c.922T>C c.1181T>C (p.Phe394Ser) n.683T>C n.797T>C c.989T>C (p.Phe330Ser) c.806T>C (p.Phe269Ser) | gnomAD v4 |
1 | g.77933451T>G | CA918823 | NEXN | c.1223T>G (p.Phe408Cys) c.1031T>G (p.Phe344Cys) c.922T>G c.1181T>G (p.Phe394Cys) n.683T>G n.797T>G c.989T>G (p.Phe330Cys) c.806T>G (p.Phe269Cys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933451T= | CA1143552818 | NEXN | c.1223T= (p.Phe408=) c.1031T= (p.Phe344=) c.922T= c.1181T= (p.Phe394=) n.683T= n.797T= c.989T= (p.Phe330=) c.806T= (p.Phe269=) | |
1 | g.77933452T>A | CA340877190 | NEXN | c.1224T>A (p.Phe408Leu) c.1032T>A (p.Phe344Leu) c.923T>A c.1182T>A (p.Phe394Leu) n.684T>A n.798T>A c.990T>A (p.Phe330Leu) c.807T>A (p.Phe269Leu) | |
1 | g.77933452T>C | CA418572121 | NEXN | c.1224T>C (p.Phe408=) c.1032T>C (p.Phe344=) c.923T>C c.1182T>C (p.Phe394=) n.684T>C n.798T>C c.990T>C (p.Phe330=) c.807T>C (p.Phe269=) | gnomAD v4 |
1 | g.77933452T>G | CA340877191 | NEXN | c.1224T>G (p.Phe408Leu) c.1032T>G (p.Phe344Leu) c.923T>G c.1182T>G (p.Phe394Leu) n.684T>G n.798T>G c.990T>G (p.Phe330Leu) c.807T>G (p.Phe269Leu) | |
1 | g.77933453G>A | CA340877193 | NEXN | c.1225G>A (p.Glu409Lys) c.1033G>A (p.Glu345Lys) c.924G>A c.1183G>A (p.Glu395Lys) n.685G>A n.799G>A c.991G>A (p.Glu331Lys) c.808G>A (p.Glu270Lys) | gnomAD v4 |
1 | g.77933453G>C | CA918824 | NEXN | c.1225G>C (p.Glu409Gln) c.1033G>C (p.Glu345Gln) c.924G>C c.1183G>C (p.Glu395Gln) n.685G>C n.799G>C c.991G>C (p.Glu331Gln) c.808G>C (p.Glu270Gln) | dbSNP ExAC gnomAD v2 |
1 | g.77933453G= | CA1177626777 | NEXN | c.1225G= (p.Glu409=) c.1033G= (p.Glu345=) c.924G= c.1183G= (p.Glu395=) n.685G= n.799G= c.991G= (p.Glu331=) c.808G= (p.Glu270=) | |
1 | g.77933453G>T | CA340877197 | NEXN | c.1225G>T (p.Glu409Ter) c.1033G>T (p.Glu345Ter) c.924G>T c.1183G>T (p.Glu395Ter) n.685G>T n.799G>T c.991G>T (p.Glu331Ter) c.808G>T (p.Glu270Ter) | gnomAD v4 |
1 | g.77933454A= | CA1177626779 | NEXN | c.1226A= (p.Glu409=) c.1034A= (p.Glu345=) c.925A= c.1184A= (p.Glu395=) n.686A= n.800A= c.992A= (p.Glu331=) c.809A= (p.Glu270=) | |
1 | g.77933454A>C | CA918825 | NEXN | c.1226A>C (p.Glu409Ala) c.1034A>C (p.Glu345Ala) c.925A>C c.1184A>C (p.Glu395Ala) n.686A>C n.800A>C c.992A>C (p.Glu331Ala) c.809A>C (p.Glu270Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933454A>G | CA340877198 | NEXN | c.1226A>G (p.Glu409Gly) c.1034A>G (p.Glu345Gly) c.925A>G c.1184A>G (p.Glu395Gly) n.686A>G n.800A>G c.992A>G (p.Glu331Gly) c.809A>G (p.Glu270Gly) | |
1 | g.77933454A>T | CA340877200 | NEXN | c.1226A>T (p.Glu409Val) c.1034A>T (p.Glu345Val) c.925A>T c.1184A>T (p.Glu395Val) n.686A>T n.800A>T c.992A>T (p.Glu331Val) c.809A>T (p.Glu270Val) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.77933457_77933459del | CA2574414092 | NEXN | c.1229_1231del (p.Gln410del) c.1037_1039del (p.Gln346del) c.928_930del c.1187_1189del (p.Gln396del) n.689_691del n.803_805del c.995_997del (p.Gln332del) c.812_814del (p.Gln271del) | |
1 | g.77933455A= | CA1149070552 | NEXN | c.1227A= (p.Glu409=) c.1035A= (p.Glu345=) c.926A= c.1185A= (p.Glu395=) n.687A= n.801A= c.993A= (p.Glu331=) c.810A= (p.Glu270=) | |
1 | g.77933455A>C | CA340877202 | NEXN | c.1227A>C (p.Glu409Asp) c.1035A>C (p.Glu345Asp) c.926A>C c.1185A>C (p.Glu395Asp) n.687A>C n.801A>C c.993A>C (p.Glu331Asp) c.810A>C (p.Glu270Asp) | |
1 | g.77933455A>G | CA418572122 | NEXN | c.1227A>G (p.Glu409=) c.1035A>G (p.Glu345=) c.926A>G c.1185A>G (p.Glu395=) n.687A>G n.801A>G c.993A>G (p.Glu331=) c.810A>G (p.Glu270=) | |
1 | g.77933455A>T | CA918826 | NEXN | c.1227A>T (p.Glu409Asp) c.1035A>T (p.Glu345Asp) c.926A>T c.1185A>T (p.Glu395Asp) n.687A>T n.801A>T c.993A>T (p.Glu331Asp) c.810A>T (p.Glu270Asp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933456C>A | CA340877206 | NEXN | c.1228C>A (p.Gln410Lys) c.1036C>A (p.Gln346Lys) c.927C>A c.1186C>A (p.Gln396Lys) n.688C>A n.802C>A c.994C>A (p.Gln332Lys) c.811C>A (p.Gln271Lys) | gnomAD v4 |
1 | g.77933456C= | CA1177626786 | NEXN | c.1228C= (p.Gln410=) c.1036C= (p.Gln346=) c.927C= c.1186C= (p.Gln396=) n.688C= n.802C= c.994C= (p.Gln332=) c.811C= (p.Gln271=) | |
1 | g.77933456C>G | CA340877208 | NEXN | c.1228C>G (p.Gln410Glu) c.1036C>G (p.Gln346Glu) c.927C>G c.1186C>G (p.Gln396Glu) n.688C>G n.802C>G c.994C>G (p.Gln332Glu) c.811C>G (p.Gln271Glu) | dbSNP |
1 | g.77933456C>T | CA340877204 | NEXN | c.1228C>T (p.Gln410Ter) c.1036C>T (p.Gln346Ter) c.927C>T c.1186C>T (p.Gln396Ter) n.688C>T n.802C>T c.994C>T (p.Gln332Ter) c.811C>T (p.Gln271Ter) | ClinVar dbSNP gnomAD v4 |
1 | g.77933457A>C | CA340877211 | NEXN | c.1229A>C (p.Gln410Pro) c.1037A>C (p.Gln346Pro) c.928A>C c.1187A>C (p.Gln396Pro) n.689A>C n.803A>C c.995A>C (p.Gln332Pro) c.812A>C (p.Gln271Pro) | |
1 | g.77933457A>G | CA340877209 | NEXN | c.1229A>G (p.Gln410Arg) c.1037A>G (p.Gln346Arg) c.928A>G c.1187A>G (p.Gln396Arg) n.689A>G n.803A>G c.995A>G (p.Gln332Arg) c.812A>G (p.Gln271Arg) | |
1 | g.77933457A>T | CA340877212 | NEXN | c.1229A>T (p.Gln410Leu) c.1037A>T (p.Gln346Leu) c.928A>T c.1187A>T (p.Gln396Leu) n.689A>T n.803A>T c.995A>T (p.Gln332Leu) c.812A>T (p.Gln271Leu) | |
1 | g.77933458A>C | CA340877214 | NEXN | c.1230A>C (p.Gln410His) c.1038A>C (p.Gln346His) c.929A>C c.1188A>C (p.Gln396His) n.690A>C n.804A>C c.996A>C (p.Gln332His) c.813A>C (p.Gln271His) | |
1 | g.77933458A>G | CA418572123 | NEXN | c.1230A>G (p.Gln410=) c.1038A>G (p.Gln346=) c.929A>G c.1188A>G (p.Gln396=) n.690A>G n.804A>G c.996A>G (p.Gln332=) c.813A>G (p.Gln271=) | |
1 | g.77933458A>T | CA340877215 | NEXN | c.1230A>T (p.Gln410His) c.1038A>T (p.Gln346His) c.929A>T c.1188A>T (p.Gln396His) n.690A>T n.804A>T c.996A>T (p.Gln332His) c.813A>T (p.Gln271His) | |
1 | g.77933459C>A | CA340877217 | NEXN | c.1231C>A (p.Leu411Met) c.1039C>A (p.Leu347Met) c.930C>A c.1189C>A (p.Leu397Met) n.691C>A n.805C>A c.997C>A (p.Leu333Met) c.814C>A (p.Leu272Met) | gnomAD v4 |
1 | g.77933459C= | CA1177626789 | NEXN | c.1231C= (p.Leu411=) c.1039C= (p.Leu347=) c.930C= c.1189C= (p.Leu397=) n.691C= n.805C= c.997C= (p.Leu333=) c.814C= (p.Leu272=) | |
1 | g.77933459C>G | CA340877218 | NEXN | c.1231C>G (p.Leu411Val) c.1039C>G (p.Leu347Val) c.930C>G c.1189C>G (p.Leu397Val) n.691C>G n.805C>G c.997C>G (p.Leu333Val) c.814C>G (p.Leu272Val) | |
1 | g.77933459C>T | CA418572124 | NEXN | c.1231C>T (p.Leu411=) c.1039C>T (p.Leu347=) c.930C>T c.1189C>T (p.Leu397=) n.691C>T n.805C>T c.997C>T (p.Leu333=) c.814C>T (p.Leu272=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.77933460T>A | CA340877220 | NEXN | c.1232T>A (p.Leu411Gln) c.1040T>A (p.Leu347Gln) c.931T>A c.1190T>A (p.Leu397Gln) n.692T>A n.806T>A c.998T>A (p.Leu333Gln) c.815T>A (p.Leu272Gln) | ClinVar dbSNP |
1 | g.77933460T>C | CA340877221 | NEXN | c.1232T>C (p.Leu411Pro) c.1040T>C (p.Leu347Pro) c.931T>C c.1190T>C (p.Leu397Pro) n.692T>C n.806T>C c.998T>C (p.Leu333Pro) c.815T>C (p.Leu272Pro) | |
1 | g.77933460T>G | CA340877223 | NEXN | c.1232T>G (p.Leu411Arg) c.1040T>G (p.Leu347Arg) c.931T>G c.1190T>G (p.Leu397Arg) n.692T>G n.806T>G c.998T>G (p.Leu333Arg) c.815T>G (p.Leu272Arg) | |
1 | g.77933460T= | CA1177626790 | NEXN | c.1232T= (p.Leu411=) c.1040T= (p.Leu347=) c.931T= c.1190T= (p.Leu397=) n.692T= n.806T= c.998T= (p.Leu333=) c.815T= (p.Leu272=) | |
1 | g.77933461G>A | CA418572125 | NEXN | c.1233G>A (p.Leu411=) c.1041G>A (p.Leu347=) c.932G>A c.1191G>A (p.Leu397=) n.693G>A n.807G>A c.999G>A (p.Leu333=) c.816G>A (p.Leu272=) | |
1 | g.77933461G>C | CA418572127 | NEXN | c.1233G>C (p.Leu411=) c.1041G>C (p.Leu347=) c.932G>C c.1191G>C (p.Leu397=) n.693G>C n.807G>C c.999G>C (p.Leu333=) c.816G>C (p.Leu272=) | |
1 | g.77933461G>T | CA418572126 | NEXN | c.1233G>T (p.Leu411=) c.1041G>T (p.Leu347=) c.932G>T c.1191G>T (p.Leu397=) n.693G>T n.807G>T c.999G>T (p.Leu333=) c.816G>T (p.Leu272=) | |
1 | g.77933461_77933462insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG | CA524231116 | NEXN | c.1233_1234insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG c.1041_1042insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG c.932_933insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG c.1191_1192insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG n.693_694insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG n.807_808insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG c.999_1000insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG c.816_817insGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG | dbSNP gnomAD v2 |
1 | g.77933461_77933462insGCCGGGCGCGGTGGCTC | CA2646274524 | NEXN | c.1233_1234insGCCGGGCGCGGTGGCTC (p.Arg412AlafsTer22) c.1041_1042insGCCGGGCGCGGTGGCTC (p.Arg348AlafsTer22) c.932_933insGCCGGGCGCGGTGGCTC c.1191_1192insGCCGGGCGCGGTGGCTC (p.Arg398AlafsTer22) n.693_694insGCCGGGCGCGGTGGCTC n.807_808insGCCGGGCGCGGTGGCTC c.1233_1234insGCCGGGCGCGGTGGCTC (p.Arg412AlafsTer32) c.999_1000insGCCGGGCGCGGTGGCTC (p.Arg334AlafsTer22) c.816_817insGCCGGGCGCGGTGGCTC (p.Arg273AlafsTer22) | gnomAD v4 |
1 | g.77933462A= | CA1177626795 | NEXN | c.1234A= (p.Arg412=) c.1042A= (p.Arg348=) c.933A= c.1192A= (p.Arg398=) n.694A= n.808A= c.1000A= (p.Arg334=) c.817A= (p.Arg273=) | |
1 | g.77933462A>C | CA418572128 | NEXN | c.1234A>C (p.Arg412=) c.1042A>C (p.Arg348=) c.933A>C c.1192A>C (p.Arg398=) n.694A>C n.808A>C c.1000A>C (p.Arg334=) c.817A>C (p.Arg273=) | |
1 | g.77933462A>G | CA918827 | NEXN | c.1234A>G (p.Arg412Gly) c.1042A>G (p.Arg348Gly) c.933A>G c.1192A>G (p.Arg398Gly) n.694A>G n.808A>G c.1000A>G (p.Arg334Gly) c.817A>G (p.Arg273Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.77933462A>T | CA340877226 | NEXN | c.1234A>T (p.Arg412Ter) c.1042A>T (p.Arg348Ter) c.933A>T c.1192A>T (p.Arg398Ter) n.694A>T n.808A>T c.1000A>T (p.Arg334Ter) c.817A>T (p.Arg273Ter) | |
1 | g.77933463G>A | CA340877227 | NEXN | c.1235G>A (p.Arg412Lys) c.1043G>A (p.Arg348Lys) c.934G>A c.1193G>A (p.Arg398Lys) n.695G>A n.809G>A c.1001G>A (p.Arg334Lys) c.818G>A (p.Arg273Lys) | |
1 | g.77933463G>C | CA340877229 | NEXN | c.1235G>C (p.Arg412Thr) c.1043G>C (p.Arg348Thr) c.934G>C c.1193G>C (p.Arg398Thr) n.695G>C n.809G>C c.1001G>C (p.Arg334Thr) c.818G>C (p.Arg273Thr) | |
1 | g.77933463G>T | CA340877230 | NEXN | c.1235G>T (p.Arg412Ile) c.1043G>T (p.Arg348Ile) c.934G>T c.1193G>T (p.Arg398Ile) n.695G>T n.809G>T c.1001G>T (p.Arg334Ile) c.818G>T (p.Arg273Ile) | |
1 | g.77933464A>C | CA340877231 | NEXN | c.1236A>C (p.Arg412Ser) c.1044A>C (p.Arg348Ser) c.935A>C c.1194A>C (p.Arg398Ser) n.696A>C n.810A>C c.1002A>C (p.Arg334Ser) c.819A>C (p.Arg273Ser) | |
1 | g.77933464A>G | CA418572129 | NEXN | c.1236A>G (p.Arg412=) c.1044A>G (p.Arg348=) c.935A>G c.1194A>G (p.Arg398=) n.696A>G n.810A>G c.1002A>G (p.Arg334=) c.819A>G (p.Arg273=) | gnomAD v4 |
1 | g.77933464A>T | CA340877233 | NEXN | c.1236A>T (p.Arg412Ser) c.1044A>T (p.Arg348Ser) c.935A>T c.1194A>T (p.Arg398Ser) n.696A>T n.810A>T c.1002A>T (p.Arg334Ser) c.819A>T (p.Arg273Ser) | |
1 | g.77933465C>A | CA340877234 | NEXN | c.1237C>A (p.Gln413Lys) c.1045C>A (p.Gln349Lys) c.936C>A c.1195C>A (p.Gln399Lys) n.697C>A n.811C>A c.1003C>A (p.Gln335Lys) c.820C>A (p.Gln274Lys) | gnomAD v4 |
1 | g.77933465C>G | CA340877237 | NEXN | c.1237C>G (p.Gln413Glu) c.1045C>G (p.Gln349Glu) c.936C>G c.1195C>G (p.Gln399Glu) n.697C>G n.811C>G c.1003C>G (p.Gln335Glu) c.820C>G (p.Gln274Glu) | |
1 | g.77933465C>T | CA340877236 | NEXN | c.1237C>T (p.Gln413Ter) c.1045C>T (p.Gln349Ter) c.936C>T c.1195C>T (p.Gln399Ter) n.697C>T n.811C>T c.1003C>T (p.Gln335Ter) c.820C>T (p.Gln274Ter) | |
1 | g.77933466A= | CA1177626797 | NEXN | c.1238A= (p.Gln413=) c.1046A= (p.Gln349=) c.937A= c.1196A= (p.Gln399=) n.698A= n.812A= c.1004A= (p.Gln335=) c.821A= (p.Gln274=) | |
1 | g.77933466A>C | CA340877239 | NEXN | c.1238A>C (p.Gln413Pro) c.1046A>C (p.Gln349Pro) c.937A>C c.1196A>C (p.Gln399Pro) n.698A>C n.812A>C c.1004A>C (p.Gln335Pro) c.821A>C (p.Gln274Pro) | |
1 | g.77933466A>G | CA340877241 | NEXN | c.1238A>G (p.Gln413Arg) c.1046A>G (p.Gln349Arg) c.937A>G c.1196A>G (p.Gln399Arg) n.698A>G n.812A>G c.1004A>G (p.Gln335Arg) c.821A>G (p.Gln274Arg) | ClinVar dbSNP gnomAD v4 |
1 | g.77933466A>T | CA340877243 | NEXN | c.1238A>T (p.Gln413Leu) c.1046A>T (p.Gln349Leu) c.937A>T c.1196A>T (p.Gln399Leu) n.698A>T n.812A>T c.1004A>T (p.Gln335Leu) c.821A>T (p.Gln274Leu) | |
1 | g.77933467G>A | CA418572130 | NEXN | c.1239G>A (p.Gln413=) c.1047G>A (p.Gln349=) c.938G>A c.1197G>A (p.Gln399=) n.699G>A n.813G>A c.1005G>A (p.Gln335=) c.822G>A (p.Gln274=) | dbSNP COSMIC COSMIC |
1 | g.77933467G>C | CA340877244 | NEXN | c.1239G>C (p.Gln413His) c.1047G>C (p.Gln349His) c.938G>C c.1197G>C (p.Gln399His) n.699G>C n.813G>C c.1005G>C (p.Gln335His) c.822G>C (p.Gln274His) | dbSNP |
1 | g.77933467G= | CA1177626799 | NEXN | c.1239G= (p.Gln413=) c.1047G= (p.Gln349=) c.938G= c.1197G= (p.Gln399=) n.699G= n.813G= c.1005G= (p.Gln335=) c.822G= (p.Gln274=) | |
1 | g.77933467G>T | CA340877246 | NEXN | c.1239G>T (p.Gln413His) c.1047G>T (p.Gln349His) c.938G>T c.1197G>T (p.Gln399His) n.699G>T n.813G>T c.1005G>T (p.Gln335His) c.822G>T (p.Gln274His) | |
1 | g.77933468G>A | CA340877247 | NEXN | c.1240G>A (p.Glu414Lys) c.1048G>A (p.Glu350Lys) c.939G>A c.1198G>A (p.Glu400Lys) n.700G>A n.814G>A c.1006G>A (p.Glu336Lys) c.823G>A (p.Glu275Lys) | gnomAD v4 |
1 | g.77933468G>C | CA918828 | NEXN | c.1240G>C (p.Glu414Gln) c.1048G>C (p.Glu350Gln) c.939G>C c.1198G>C (p.Glu400Gln) n.700G>C n.814G>C c.1006G>C (p.Glu336Gln) c.823G>C (p.Glu275Gln) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.77933468G= | CA1177626803 | NEXN | c.1240G= (p.Glu414=) c.1048G= (p.Glu350=) c.939G= c.1198G= (p.Glu400=) n.700G= n.814G= c.1006G= (p.Glu336=) c.823G= (p.Glu275=) | |
1 | g.77933468G>T | CA340877249 | NEXN | c.1240G>T (p.Glu414Ter) c.1048G>T (p.Glu350Ter) c.939G>T c.1198G>T (p.Glu400Ter) n.700G>T n.814G>T c.1006G>T (p.Glu336Ter) c.823G>T (p.Glu275Ter) | |
1 | g.77933469A>C | CA340877251 | NEXN | c.1241A>C (p.Glu414Ala) c.1049A>C (p.Glu350Ala) c.940A>C c.1199A>C (p.Glu400Ala) n.701A>C n.815A>C c.1007A>C (p.Glu336Ala) c.824A>C (p.Glu275Ala) | |
1 | g.77933469A>G | CA340877253 | NEXN | c.1241A>G (p.Glu414Gly) c.1049A>G (p.Glu350Gly) c.940A>G c.1199A>G (p.Glu400Gly) n.701A>G n.815A>G c.1007A>G (p.Glu336Gly) c.824A>G (p.Glu275Gly) | |
1 | g.77933469A>T | CA340877255 | NEXN | c.1241A>T (p.Glu414Val) c.1049A>T (p.Glu350Val) c.940A>T c.1199A>T (p.Glu400Val) n.701A>T n.815A>T c.1007A>T (p.Glu336Val) c.824A>T (p.Glu275Val) | |
1 | g.77933470A= | CA1177626805 | NEXN | c.1242A= (p.Glu414=) c.1050A= (p.Glu350=) c.941A= c.1200A= (p.Glu400=) n.702A= n.816A= c.1008A= (p.Glu336=) c.825A= (p.Glu275=) | |
1 | g.77933470A>C | CA340877256 | NEXN | c.1242A>C (p.Glu414Asp) c.1050A>C (p.Glu350Asp) c.941A>C c.1200A>C (p.Glu400Asp) n.702A>C n.816A>C c.1008A>C (p.Glu336Asp) c.825A>C (p.Glu275Asp) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
1 | g.77933470A>G | CA418572131 | NEXN | c.1242A>G (p.Glu414=) c.1050A>G (p.Glu350=) c.941A>G c.1200A>G (p.Glu400=) n.702A>G n.816A>G c.1008A>G (p.Glu336=) c.825A>G (p.Glu275=) | |
1 | g.77933470A>T | CA340877258 | NEXN | c.1242A>T (p.Glu414Asp) c.1050A>T (p.Glu350Asp) c.941A>T c.1200A>T (p.Glu400Asp) n.702A>T n.816A>T c.1008A>T (p.Glu336Asp) c.825A>T (p.Glu275Asp) | |
1 | g.77933471A>C | CA340877259 | NEXN | c.1243A>C (p.Met415Leu) c.1051A>C (p.Met351Leu) c.942A>C c.1201A>C (p.Met401Leu) n.703A>C n.817A>C c.1009A>C (p.Met337Leu) c.826A>C (p.Met276Leu) | |
1 | g.77933471A>G | CA340877261 | NEXN | c.1243A>G (p.Met415Val) c.1051A>G (p.Met351Val) c.942A>G c.1201A>G (p.Met401Val) n.703A>G n.817A>G c.1009A>G (p.Met337Val) c.826A>G (p.Met276Val) | |
1 | g.77933471A>T | CA340877262 | NEXN | c.1243A>T (p.Met415Leu) c.1051A>T (p.Met351Leu) c.942A>T c.1201A>T (p.Met401Leu) n.703A>T n.817A>T c.1009A>T (p.Met337Leu) c.826A>T (p.Met276Leu) | |
1 | g.77933472T>A | CA340877264 | NEXN | c.1244T>A (p.Met415Lys) c.1052T>A (p.Met351Lys) c.943T>A c.1202T>A (p.Met401Lys) n.704T>A n.818T>A c.1010T>A (p.Met337Lys) c.827T>A (p.Met276Lys) | |
1 | g.77933472T>C | CA340877266 | NEXN | c.1244T>C (p.Met415Thr) c.1052T>C (p.Met351Thr) c.943T>C c.1202T>C (p.Met401Thr) n.704T>C n.818T>C c.1010T>C (p.Met337Thr) c.827T>C (p.Met276Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
1 | g.77933472T>G | CA340877268 | NEXN | c.1244T>G (p.Met415Arg) c.1052T>G (p.Met351Arg) c.943T>G c.1202T>G (p.Met401Arg) n.704T>G n.818T>G c.1010T>G (p.Met337Arg) c.827T>G (p.Met276Arg) | |
1 | g.77933472T= | CA1177626807 | NEXN | c.1244T= (p.Met415=) c.1052T= (p.Met351=) c.943T= c.1202T= (p.Met401=) n.704T= n.818T= c.1010T= (p.Met337=) c.827T= (p.Met276=) | |
1 | g.77933473G>A | CA340877269 | NEXN | c.1245G>A (p.Met415Ile) c.1053G>A (p.Met351Ile) c.944G>A c.1203G>A (p.Met401Ile) n.705G>A n.819G>A c.1011G>A (p.Met337Ile) c.828G>A (p.Met276Ile) | |
1 | g.77933473G>C | CA340877271 | NEXN | c.1245G>C (p.Met415Ile) c.1053G>C (p.Met351Ile) c.944G>C c.1203G>C (p.Met401Ile) n.705G>C n.819G>C c.1011G>C (p.Met337Ile) c.828G>C (p.Met276Ile) | |
1 | g.77933473G>T | CA340877273 | NEXN | c.1245G>T (p.Met415Ile) c.1053G>T (p.Met351Ile) c.944G>T c.1203G>T (p.Met401Ile) n.705G>T n.819G>T c.1011G>T (p.Met337Ile) c.828G>T (p.Met276Ile) | gnomAD v4 |
1 | g.77933474G>A | CA340877275 | NEXN | c.1246G>A (p.Gly416Arg) c.1054G>A (p.Gly352Arg) c.945G>A c.1204G>A (p.Gly402Arg) n.706G>A n.820G>A c.1012G>A (p.Gly338Arg) c.829G>A (p.Gly277Arg) | gnomAD v4 COSMIC COSMIC |
1 | g.77933474G>C | CA340877276 | NEXN | c.1246G>C (p.Gly416Arg) c.1054G>C (p.Gly352Arg) c.945G>C c.1204G>C (p.Gly402Arg) n.706G>C n.820G>C c.1012G>C (p.Gly338Arg) c.829G>C (p.Gly277Arg) | |
1 | g.77933474G>T | CA340877277 | NEXN | c.1246G>T (p.Gly416Ter) c.1054G>T (p.Gly352Ter) c.945G>T c.1204G>T (p.Gly402Ter) n.706G>T n.820G>T c.1012G>T (p.Gly338Ter) c.829G>T (p.Gly277Ter) | |
1 | g.77933475G>A | CA340877279 | NEXN | c.1247G>A (p.Gly416Glu) c.1055G>A (p.Gly352Glu) c.946G>A c.1205G>A (p.Gly402Glu) n.707G>A n.821G>A c.1013G>A (p.Gly338Glu) c.830G>A (p.Gly277Glu) | dbSNP gnomAD v4 |
1 | g.77933475G>C | CA340877280 | NEXN | c.1247G>C (p.Gly416Ala) c.1055G>C (p.Gly352Ala) c.946G>C c.1205G>C (p.Gly402Ala) n.707G>C n.821G>C c.1013G>C (p.Gly338Ala) c.830G>C (p.Gly277Ala) | |
1 | g.77933475G= | CA1177626810 | NEXN | c.1247G= (p.Gly416=) c.1055G= (p.Gly352=) c.946G= c.1205G= (p.Gly402=) n.707G= n.821G= c.1013G= (p.Gly338=) c.830G= (p.Gly277=) | |
1 | g.77933475G>T | CA340877278 | NEXN | c.1247G>T (p.Gly416Val) c.1055G>T (p.Gly352Val) c.946G>T c.1205G>T (p.Gly402Val) n.707G>T n.821G>T c.1013G>T (p.Gly338Val) c.830G>T (p.Gly277Val) | |
1 | g.77933476A>C | CA418572135 | NEXN | c.1248A>C (p.Gly416=) c.1056A>C (p.Gly352=) c.947A>C c.1206A>C (p.Gly402=) n.708A>C n.822A>C c.1014A>C (p.Gly338=) c.831A>C (p.Gly277=) | |
1 | g.77933476A>G | CA418572133 | NEXN | c.1248A>G (p.Gly416=) c.1056A>G (p.Gly352=) c.947A>G c.1206A>G (p.Gly402=) n.708A>G n.822A>G c.1014A>G (p.Gly338=) c.831A>G (p.Gly277=) | |
1 | g.77933476A>T | CA418572134 | NEXN | c.1248A>T (p.Gly416=) c.1056A>T (p.Gly352=) c.947A>T c.1206A>T (p.Gly402=) n.708A>T n.822A>T c.1014A>T (p.Gly338=) c.831A>T (p.Gly277=) | |
1 | g.77933476_77933477insTTTCTTTTTTTTGTTT | CA2646274525 | NEXN | c.1248_1249insTTTCTTTTTTTTGTTT (p.Glu417PhefsTer6) c.1056_1057insTTTCTTTTTTTTGTTT (p.Glu353PhefsTer6) c.947_948insTTTCTTTTTTTTGTTT c.1206_1207insTTTCTTTTTTTTGTTT (p.Glu403PhefsTer6) n.708_709insTTTCTTTTTTTTGTTT n.822_823insTTTCTTTTTTTTGTTT c.1014_1015insTTTCTTTTTTTTGTTT (p.Glu339PhefsTer6) c.831_832insTTTCTTTTTTTTGTTT (p.Glu278PhefsTer6) | gnomAD v4 |
1 | g.77933477G>A | CA24684369 | NEXN | c.1249G>A (p.Glu417Lys) c.1057G>A (p.Glu353Lys) c.948G>A c.1207G>A (p.Glu403Lys) n.709G>A n.823G>A c.1015G>A (p.Glu339Lys) c.832G>A (p.Glu278Lys) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933477G>C | CA340877281 | NEXN | c.1249G>C (p.Glu417Gln) c.1057G>C (p.Glu353Gln) c.948G>C c.1207G>C (p.Glu403Gln) n.709G>C n.823G>C c.1015G>C (p.Glu339Gln) c.832G>C (p.Glu278Gln) | gnomAD v4 |
1 | g.77933477G= | CA1177626813 | NEXN | c.1249G= (p.Glu417=) c.1057G= (p.Glu353=) c.948G= c.1207G= (p.Glu403=) n.709G= n.823G= c.1015G= (p.Glu339=) c.832G= (p.Glu278=) | |
1 | g.77933477G>T | CA340877282 | NEXN | c.1249G>T (p.Glu417Ter) c.1057G>T (p.Glu353Ter) c.948G>T c.1207G>T (p.Glu403Ter) n.709G>T n.823G>T c.1015G>T (p.Glu339Ter) c.832G>T (p.Glu278Ter) | |
1 | g.77933478A>C | CA340877283 | NEXN | c.1250A>C (p.Glu417Ala) c.1058A>C (p.Glu353Ala) c.949A>C c.1208A>C (p.Glu403Ala) n.710A>C n.824A>C c.1016A>C (p.Glu339Ala) c.833A>C (p.Glu278Ala) | |
1 | g.77933478A>G | CA340877284 | NEXN | c.1250A>G (p.Glu417Gly) c.1058A>G (p.Glu353Gly) c.949A>G c.1208A>G (p.Glu403Gly) n.710A>G n.824A>G c.1016A>G (p.Glu339Gly) c.833A>G (p.Glu278Gly) | gnomAD v4 |
1 | g.77933478A>T | CA340877285 | NEXN | c.1250A>T (p.Glu417Val) c.1058A>T (p.Glu353Val) c.949A>T c.1208A>T (p.Glu403Val) n.710A>T n.824A>T c.1016A>T (p.Glu339Val) c.833A>T (p.Glu278Val) | gnomAD v4 |
1 | g.77933479G>A | CA418572136 | NEXN | c.1251G>A (p.Glu417=) c.1059G>A (p.Glu353=) c.950G>A c.1209G>A (p.Glu403=) n.711G>A n.825G>A c.1017G>A (p.Glu339=) c.834G>A (p.Glu278=) | |
1 | g.77933479G>C | CA340877286 | NEXN | c.1251G>C (p.Glu417Asp) c.1059G>C (p.Glu353Asp) c.950G>C c.1209G>C (p.Glu403Asp) n.711G>C n.825G>C c.1017G>C (p.Glu339Asp) c.834G>C (p.Glu278Asp) | |
1 | g.77933479G>T | CA340877287 | NEXN | c.1251G>T (p.Glu417Asp) c.1059G>T (p.Glu353Asp) c.950G>T c.1209G>T (p.Glu403Asp) n.711G>T n.825G>T c.1017G>T (p.Glu339Asp) c.834G>T (p.Glu278Asp) | gnomAD v4 |
1 | g.77933480del | CA2573131973 | NEXN | c.1251+1del c.1059+1del c.950+1del c.1209+1del n.711+1del n.825+1del c.1017+1del c.834+1del | ClinVar dbSNP |
1 | g.77933480G>A | CA340877289 | NEXN | c.1251+1G>A (n.1251+1G>A) c.1059+1G>A (n.1059+1G>A) c.950+1G>A c.1209+1G>A (n.1209+1G>A) n.711+1G>A n.825+1G>A c.1017+1G>A (n.1017+1G>A) c.834+1G>A (n.834+1G>A) | ClinVar dbSNP |
1 | g.77933480G>C | CA340877291 | NEXN | c.1251+1G>C (n.1251+1G>C) c.1059+1G>C (n.1059+1G>C) c.950+1G>C c.1209+1G>C (n.1209+1G>C) n.711+1G>C n.825+1G>C c.1017+1G>C (n.1017+1G>C) c.834+1G>C (n.834+1G>C) | gnomAD v4 |
1 | g.77933480G= | CA1177626815 | NEXN | c.1251+1G= (n.1251+1G=) c.1059+1G= (n.1059+1G=) c.950+1G= c.1209+1G= (n.1209+1G=) n.711+1G= n.825+1G= c.1017+1G= (n.1017+1G=) c.834+1G= (n.834+1G=) | |
1 | g.77933480G>T | CA340877293 | NEXN | c.1251+1G>T (n.1251+1G>T) c.1059+1G>T (n.1059+1G>T) c.950+1G>T c.1209+1G>T (n.1209+1G>T) n.711+1G>T n.825+1G>T c.1017+1G>T (n.1017+1G>T) c.834+1G>T (n.834+1G>T) | gnomAD v4 |
1 | g.77933481T>A | CA24684370 | NEXN | c.1251+2T>A (n.1251+2T>A) c.1059+2T>A (n.1059+2T>A) c.950+2T>A c.1209+2T>A (n.1209+2T>A) n.711+2T>A n.825+2T>A c.1017+2T>A (n.1017+2T>A) c.834+2T>A (n.834+2T>A) | dbSNP |
1 | g.77933481T>C | CA340877297 | NEXN | c.1251+2T>C (n.1251+2T>C) c.1059+2T>C (n.1059+2T>C) c.950+2T>C c.1209+2T>C (n.1209+2T>C) n.711+2T>C n.825+2T>C c.1017+2T>C (n.1017+2T>C) c.834+2T>C (n.834+2T>C) | |
1 | g.77933481T>G | CA340877299 | NEXN | c.1251+2T>G (n.1251+2T>G) c.1059+2T>G (n.1059+2T>G) c.950+2T>G c.1209+2T>G (n.1209+2T>G) n.711+2T>G n.825+2T>G c.1017+2T>G (n.1017+2T>G) c.834+2T>G (n.834+2T>G) | gnomAD v4 |
1 | g.77933481T= | CA1141242283 | NEXN | c.1251+2T= (n.1251+2T=) c.1059+2T= (n.1059+2T=) c.950+2T= c.1209+2T= (n.1209+2T=) n.711+2T= n.825+2T= c.1017+2T= (n.1017+2T=) c.834+2T= (n.834+2T=) | |
1 | g.77933482A= | CA1177626819 | NEXN | c.1251+3A= (n.1251+3A=) c.1059+3A= (n.1059+3A=) c.950+3A= c.1209+3A= (n.1209+3A=) n.711+3A= n.825+3A= c.1017+3A= (n.1017+3A=) c.834+3A= (n.834+3A=) | |
1 | g.77933482A>C | CA739053521 | NEXN | c.1251+3A>C (n.1251+3A>C) c.1059+3A>C (n.1059+3A>C) c.950+3A>C c.1209+3A>C (n.1209+3A>C) n.711+3A>C n.825+3A>C c.1017+3A>C (n.1017+3A>C) c.834+3A>C (n.834+3A>C) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.77933482A>G | CA2646274526 | NEXN | c.1251+3A>G (n.1251+3A>G) c.1059+3A>G (n.1059+3A>G) c.950+3A>G c.1209+3A>G (n.1209+3A>G) n.711+3A>G n.825+3A>G c.1017+3A>G (n.1017+3A>G) c.834+3A>G (n.834+3A>G) | gnomAD v4 |
1 | g.77933482A>T | CA2646274527 | NEXN | c.1251+3A>T (n.1251+3A>T) c.1059+3A>T (n.1059+3A>T) c.950+3A>T c.1209+3A>T (n.1209+3A>T) n.711+3A>T n.825+3A>T c.1017+3A>T (n.1017+3A>T) c.834+3A>T (n.834+3A>T) | gnomAD v4 |
1 | g.77933484G= | CA1177626820 | NEXN | c.1251+5G= (n.1251+5G=) c.1059+5G= (n.1059+5G=) c.950+5G= c.1209+5G= (n.1209+5G=) n.711+5G= n.825+5G= c.1017+5G= (n.1017+5G=) c.834+5G= (n.834+5G=) | |
1 | g.77933485A>G | CA2646274528 | NEXN | c.1251+6A>G (n.1251+6A>G) c.1059+6A>G (n.1059+6A>G) c.950+6A>G c.1209+6A>G (n.1209+6A>G) n.711+6A>G n.825+6A>G c.1017+6A>G (n.1017+6A>G) c.834+6A>G (n.834+6A>G) | gnomAD v4 |
1 | g.77933485A>T | CA2646274529 | NEXN | c.1251+6A>T (n.1251+6A>T) c.1059+6A>T (n.1059+6A>T) c.950+6A>T c.1209+6A>T (n.1209+6A>T) n.711+6A>T n.825+6A>T c.1017+6A>T (n.1017+6A>T) c.834+6A>T (n.834+6A>T) | gnomAD v4 |
1 | g.77933485_77933486insAA | CA524231117 | NEXN | c.1251+6_1251+7insAA (n.1251+6_1251+7insAA) c.1059+6_1059+7insAA (n.1059+6_1059+7insAA) c.950+6_950+7insAA c.1209+6_1209+7insAA (n.1209+6_1209+7insAA) n.711+6_711+7insAA n.825+6_825+7insAA c.1017+6_1017+7insAA (n.1017+6_1017+7insAA) c.834+6_834+7insAA (n.834+6_834+7insAA) | dbSNP gnomAD v2 |
1 | g.77933485_77933486insC | CA2527946704 | NEXN | c.1251+6_1251+7insC (n.1251+6_1251+7insC) c.1059+6_1059+7insC (n.1059+6_1059+7insC) c.950+6_950+7insC c.1209+6_1209+7insC (n.1209+6_1209+7insC) n.711+6_711+7insC n.825+6_825+7insC c.1017+6_1017+7insC (n.1017+6_1017+7insC) c.834+6_834+7insC (n.834+6_834+7insC) | |
1 | g.77933485_77933486insGGGGTATTATTCATTTGCTCCAAG | CA2744232066 | NEXN | c.1251+6_1251+7insGGGGTATTATTCATTTGCTCCAAG (n.1251+6_1251+7insGGGGTATTATTCATTTGCTCCAAG) c.1059+6_1059+7insGGGGTATTATTCATTTGCTCCAAG (n.1059+6_1059+7insGGGGTATTATTCATTTGCTCCAAG) c.950+6_950+7insGGGGTATTATTCATTTGCTCCAAG c.1209+6_1209+7insGGGGTATTATTCATTTGCTCCAAG (n.1209+6_1209+7insGGGGTATTATTCATTTGCTCCAAG) n.711+6_711+7insGGGGTATTATTCATTTGCTCCAAG n.825+6_825+7insGGGGTATTATTCATTTGCTCCAAG c.1017+6_1017+7insGGGGTATTATTCATTTGCTCCAAG (n.1017+6_1017+7insGGGGTATTATTCATTTGCTCCAAG) c.834+6_834+7insGGGGTATTATTCATTTGCTCCAAG (n.834+6_834+7insGGGGTATTATTCATTTGCTCCAAG) | |
1 | g.77933486T>C | CA2646274532 | NEXN | c.1251+7T>C (n.1251+7T>C) c.1059+7T>C (n.1059+7T>C) c.950+7T>C c.1209+7T>C (n.1209+7T>C) n.711+7T>C n.825+7T>C c.1017+7T>C (n.1017+7T>C) c.834+7T>C (n.834+7T>C) | gnomAD v4 |
1 | g.77933489dup | CA2646274530 | NEXN | c.1251+10dup (n.1251+10dup) c.1059+10dup (n.1059+10dup) c.950+10dup c.1209+10dup (n.1209+10dup) n.711+10dup n.825+10dup c.1017+10dup (n.1017+10dup) c.834+10dup (n.834+10dup) | gnomAD v4 |
1 | g.77933489del | CA2646274531 | NEXN | c.1251+10del (n.1251+10del) c.1059+10del (n.1059+10del) c.950+10del c.1209+10del (n.1209+10del) n.711+10del n.825+10del c.1017+10del (n.1017+10del) c.834+10del (n.834+10del) | gnomAD v4 |
1 | g.77933487T= | CA1177626822 | NEXN | c.1251+8T= (n.1251+8T=) c.1059+8T= (n.1059+8T=) c.950+8T= c.1209+8T= (n.1209+8T=) n.711+8T= n.825+8T= c.1017+8T= (n.1017+8T=) c.834+8T= (n.834+8T=) | |
1 | g.77933487_77933488insC | CA524231118 | NEXN | c.1251+8_1251+9insC (n.1251+8_1251+9insC) c.1059+8_1059+9insC (n.1059+8_1059+9insC) c.950+8_950+9insC c.1209+8_1209+9insC (n.1209+8_1209+9insC) n.711+8_711+9insC n.825+8_825+9insC c.1017+8_1017+9insC (n.1017+8_1017+9insC) c.834+8_834+9insC (n.834+8_834+9insC) | dbSNP gnomAD v2 |
1 | g.77933487_77933488insCTTGAGAGATTGTC | CA918829 | NEXN | c.1251+8_1251+9insCTTGAGAGATTGTC (n.1251+8_1251+9insCTTGAGAGATTGTC) c.1059+8_1059+9insCTTGAGAGATTGTC (n.1059+8_1059+9insCTTGAGAGATTGTC) c.950+8_950+9insCTTGAGAGATTGTC c.1209+8_1209+9insCTTGAGAGATTGTC (n.1209+8_1209+9insCTTGAGAGATTGTC) n.711+8_711+9insCTTGAGAGATTGTC n.825+8_825+9insCTTGAGAGATTGTC c.1017+8_1017+9insCTTGAGAGATTGTC (n.1017+8_1017+9insCTTGAGAGATTGTC) c.834+8_834+9insCTTGAGAGATTGTC (n.834+8_834+9insCTTGAGAGATTGTC) | dbSNP ExAC |
1 | g.77933488T>C | CA524231119 | NEXN | c.1251+9T>C (n.1251+9T>C) c.1059+9T>C (n.1059+9T>C) c.950+9T>C c.1209+9T>C (n.1209+9T>C) n.711+9T>C n.825+9T>C c.1017+9T>C (n.1017+9T>C) c.834+9T>C (n.834+9T>C) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.77933488T= | CA1177626824 | NEXN | c.1251+9T= (n.1251+9T=) c.1059+9T= (n.1059+9T=) c.950+9T= c.1209+9T= (n.1209+9T=) n.711+9T= n.825+9T= c.1017+9T= (n.1017+9T=) c.834+9T= (n.834+9T=) | |
1 | g.77933489T>A | CA2646274533 | NEXN | c.1251+10T>A (n.1251+10T>A) c.1059+10T>A (n.1059+10T>A) c.950+10T>A c.1209+10T>A (n.1209+10T>A) n.711+10T>A n.825+10T>A c.1017+10T>A (n.1017+10T>A) c.834+10T>A (n.834+10T>A) | gnomAD v4 |
1 | g.77933489T>C | CA524231120 | NEXN | c.1251+10T>C (n.1251+10T>C) c.1059+10T>C (n.1059+10T>C) c.950+10T>C c.1209+10T>C (n.1209+10T>C) n.711+10T>C n.825+10T>C c.1017+10T>C (n.1017+10T>C) c.834+10T>C (n.834+10T>C) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933489T= | CA1177626826 | NEXN | c.1251+10T= (n.1251+10T=) c.1059+10T= (n.1059+10T=) c.950+10T= c.1209+10T= (n.1209+10T=) n.711+10T= n.825+10T= c.1017+10T= (n.1017+10T=) c.834+10T= (n.834+10T=) | |
1 | g.77933490A= | CA1177626827 | NEXN | c.1251+11A= (n.1251+11A=) c.1059+11A= (n.1059+11A=) c.950+11A= c.1209+11A= (n.1209+11A=) n.711+11A= n.825+11A= c.1017+11A= (n.1017+11A=) c.834+11A= (n.834+11A=) | |
1 | g.77933490A>G | CA524231121 | NEXN | c.1251+11A>G (n.1251+11A>G) c.1059+11A>G (n.1059+11A>G) c.950+11A>G c.1209+11A>G (n.1209+11A>G) n.711+11A>G n.825+11A>G c.1017+11A>G (n.1017+11A>G) c.834+11A>G (n.834+11A>G) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.77933492del | CA2503023172 | NEXN | c.1251+13del (n.1251+13del) c.1059+13del (n.1059+13del) c.950+13del c.1209+13del (n.1209+13del) n.711+13del n.825+13del c.1017+13del (n.1017+13del) c.834+13del (n.834+13del) | |
1 | g.77933492G>C | CA2646274534 | NEXN | c.1251+13G>C (n.1251+13G>C) c.1059+13G>C (n.1059+13G>C) c.950+13G>C c.1209+13G>C (n.1209+13G>C) n.711+13G>C n.825+13G>C c.1017+13G>C (n.1017+13G>C) c.834+13G>C (n.834+13G>C) | gnomAD v4 |
1 | g.77933492G= | CA1148568766 | NEXN | c.1251+13G= (n.1251+13G=) c.1059+13G= (n.1059+13G=) c.950+13G= c.1209+13G= (n.1209+13G=) n.711+13G= n.825+13G= c.1017+13G= (n.1017+13G=) c.834+13G= (n.834+13G=) | |
1 | g.77933492G>T | CA918830 | NEXN | c.1251+13G>T (n.1251+13G>T) c.1059+13G>T (n.1059+13G>T) c.950+13G>T c.1209+13G>T (n.1209+13G>T) n.711+13G>T n.825+13G>T c.1017+13G>T (n.1017+13G>T) c.834+13G>T (n.834+13G>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933493A>G | CA2646274535 | NEXN | c.1251+14A>G (n.1251+14A>G) c.1059+14A>G (n.1059+14A>G) c.950+14A>G c.1209+14A>G (n.1209+14A>G) n.711+14A>G n.825+14A>G c.1017+14A>G (n.1017+14A>G) c.834+14A>G (n.834+14A>G) | gnomAD v4 |
1 | g.77933494A>G | CA2534683514 | NEXN | c.1251+15A>G (n.1251+15A>G) c.1059+15A>G (n.1059+15A>G) c.950+15A>G c.1209+15A>G (n.1209+15A>G) n.711+15A>G n.825+15A>G c.1017+15A>G (n.1017+15A>G) c.834+15A>G (n.834+15A>G) | gnomAD v4 |
1 | g.77933495A= | CA1177626828 | NEXN | c.1251+16A= (n.1251+16A=) c.1059+16A= (n.1059+16A=) c.950+16A= c.1209+16A= (n.1209+16A=) n.711+16A= n.825+16A= c.1017+16A= (n.1017+16A=) c.834+16A= (n.834+16A=) | |
1 | g.77933495A>G | CA524231122 | NEXN | c.1251+16A>G (n.1251+16A>G) c.1059+16A>G (n.1059+16A>G) c.950+16A>G c.1209+16A>G (n.1209+16A>G) n.711+16A>G n.825+16A>G c.1017+16A>G (n.1017+16A>G) c.834+16A>G (n.834+16A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933495A>T | CA2744232067 | NEXN | c.1251+16A>T (n.1251+16A>T) c.1059+16A>T (n.1059+16A>T) c.950+16A>T c.1209+16A>T (n.1209+16A>T) n.711+16A>T n.825+16A>T c.1017+16A>T (n.1017+16A>T) c.834+16A>T (n.834+16A>T) | |
1 | g.77933497A>G | CA2646274536 | NEXN | c.1251+18A>G (n.1251+18A>G) c.1059+18A>G (n.1059+18A>G) c.950+18A>G c.1209+18A>G (n.1209+18A>G) n.711+18A>G n.825+18A>G c.1017+18A>G (n.1017+18A>G) c.834+18A>G (n.834+18A>G) | gnomAD v4 |
1 | g.77933497A>T | CA2744232068 | NEXN | c.1251+18A>T (n.1251+18A>T) c.1059+18A>T (n.1059+18A>T) c.950+18A>T c.1209+18A>T (n.1209+18A>T) n.711+18A>T n.825+18A>T c.1017+18A>T (n.1017+18A>T) c.834+18A>T (n.834+18A>T) | |
1 | g.77933498T>C | CA739053538 | NEXN | c.1251+19T>C (n.1251+19T>C) c.1059+19T>C (n.1059+19T>C) c.950+19T>C c.1209+19T>C (n.1209+19T>C) n.711+19T>C n.825+19T>C c.1017+19T>C (n.1017+19T>C) c.834+19T>C (n.834+19T>C) | dbSNP gnomAD v4 |
1 | g.77933498T= | CA1177626830 | NEXN | c.1251+19T= (n.1251+19T=) c.1059+19T= (n.1059+19T=) c.950+19T= c.1209+19T= (n.1209+19T=) n.711+19T= n.825+19T= c.1017+19T= (n.1017+19T=) c.834+19T= (n.834+19T=) | |
1 | g.77933499C>A | CA2646274537 | NEXN | c.1251+20C>A (n.1251+20C>A) c.1059+20C>A (n.1059+20C>A) c.950+20C>A c.1209+20C>A (n.1209+20C>A) n.711+20C>A n.825+20C>A c.1017+20C>A (n.1017+20C>A) c.834+20C>A (n.834+20C>A) | gnomAD v4 |
1 | g.77933499C= | CA1177626831 | NEXN | c.1251+20C= (n.1251+20C=) c.1059+20C= (n.1059+20C=) c.950+20C= c.1209+20C= (n.1209+20C=) n.711+20C= n.825+20C= c.1017+20C= (n.1017+20C=) c.834+20C= (n.834+20C=) | |
1 | g.77933499C>T | CA1177626832 | NEXN | c.1251+20C>T (n.1251+20C>T) c.1059+20C>T (n.1059+20C>T) c.950+20C>T c.1209+20C>T (n.1209+20C>T) n.711+20C>T n.825+20C>T c.1017+20C>T (n.1017+20C>T) c.834+20C>T (n.834+20C>T) | dbSNP gnomAD v4 |
1 | g.77933499_77933500insCAG | CA2525338688 | NEXN | c.1251+20_1251+21insCAG (n.1251+20_1251+21insCAG) c.1059+20_1059+21insCAG (n.1059+20_1059+21insCAG) c.950+20_950+21insCAG c.1209+20_1209+21insCAG (n.1209+20_1209+21insCAG) n.711+20_711+21insCAG n.825+20_825+21insCAG c.1017+20_1017+21insCAG (n.1017+20_1017+21insCAG) c.834+20_834+21insCAG (n.834+20_834+21insCAG) | |
1 | g.77933500T>G | CA2646274538 | NEXN | c.1251+21T>G (n.1251+21T>G) c.1059+21T>G (n.1059+21T>G) c.950+21T>G c.1209+21T>G (n.1209+21T>G) n.711+21T>G n.825+21T>G c.1017+21T>G (n.1017+21T>G) c.834+21T>G (n.834+21T>G) | gnomAD v4 |
1 | g.77933500_77933501insG | CA2544064524 | NEXN | c.1251+21_1251+22insG (n.1251+21_1251+22insG) c.1059+21_1059+22insG (n.1059+21_1059+22insG) c.950+21_950+22insG c.1209+21_1209+22insG (n.1209+21_1209+22insG) n.711+21_711+22insG n.825+21_825+22insG c.1017+21_1017+22insG (n.1017+21_1017+22insG) c.834+21_834+22insG (n.834+21_834+22insG) | |
1 | g.77933501del | CA2744232069 | NEXN | c.1251+22del (n.1251+22del) c.1059+22del (n.1059+22del) c.950+22del c.1209+22del (n.1209+22del) n.711+22del n.825+22del c.1017+22del (n.1017+22del) c.834+22del (n.834+22del) | |
1 | g.77933501A>T | CA2646274539 | NEXN | c.1251+22A>T (n.1251+22A>T) c.1059+22A>T (n.1059+22A>T) c.950+22A>T c.1209+22A>T (n.1209+22A>T) n.711+22A>T n.825+22A>T c.1017+22A>T (n.1017+22A>T) c.834+22A>T (n.834+22A>T) | gnomAD v4 |
1 | g.77933502T>C | CA1177626834 | NEXN | c.1251+23T>C (n.1251+23T>C) c.1059+23T>C (n.1059+23T>C) c.950+23T>C c.1209+23T>C (n.1209+23T>C) n.711+23T>C n.825+23T>C c.1017+23T>C (n.1017+23T>C) c.834+23T>C (n.834+23T>C) | dbSNP |
1 | g.77933502T= | CA1177626833 | NEXN | c.1251+23T= (n.1251+23T=) c.1059+23T= (n.1059+23T=) c.950+23T= c.1209+23T= (n.1209+23T=) n.711+23T= n.825+23T= c.1017+23T= (n.1017+23T=) c.834+23T= (n.834+23T=) | |
1 | g.77933503A>G | CA2646274540 | NEXN | c.1251+24A>G (n.1251+24A>G) c.1059+24A>G (n.1059+24A>G) c.950+24A>G c.1209+24A>G (n.1209+24A>G) n.711+24A>G n.825+24A>G c.1017+24A>G (n.1017+24A>G) c.834+24A>G (n.834+24A>G) | gnomAD v4 |
1 | g.77933504T>A | CA2646274541 | NEXN | c.1251+25T>A (n.1251+25T>A) c.1059+25T>A (n.1059+25T>A) c.950+25T>A c.1209+25T>A (n.1209+25T>A) n.711+25T>A n.825+25T>A c.1017+25T>A (n.1017+25T>A) c.834+25T>A (n.834+25T>A) | gnomAD v4 |
1 | g.77933504T>C | CA2574414093 | NEXN | c.1251+25T>C (n.1251+25T>C) c.1059+25T>C (n.1059+25T>C) c.950+25T>C c.1209+25T>C (n.1209+25T>C) n.711+25T>C n.825+25T>C c.1017+25T>C (n.1017+25T>C) c.834+25T>C (n.834+25T>C) | gnomAD v4 |
1 | g.77933504T>G | CA2646274542 | NEXN | c.1251+25T>G (n.1251+25T>G) c.1059+25T>G (n.1059+25T>G) c.950+25T>G c.1209+25T>G (n.1209+25T>G) n.711+25T>G n.825+25T>G c.1017+25T>G (n.1017+25T>G) c.834+25T>G (n.834+25T>G) | gnomAD v4 |
1 | g.77933505T>A | CA2646274543 | NEXN | c.1251+26T>A (n.1251+26T>A) c.1059+26T>A (n.1059+26T>A) c.950+26T>A c.1209+26T>A (n.1209+26T>A) n.711+26T>A n.825+26T>A c.1017+26T>A (n.1017+26T>A) c.834+26T>A (n.834+26T>A) | gnomAD v4 |
1 | g.77933505T>C | CA739053542 | NEXN | c.1251+26T>C (n.1251+26T>C) c.1059+26T>C (n.1059+26T>C) c.950+26T>C c.1209+26T>C (n.1209+26T>C) n.711+26T>C n.825+26T>C c.1017+26T>C (n.1017+26T>C) c.834+26T>C (n.834+26T>C) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.77933505T>G | CA918831 | NEXN | c.1251+26T>G (n.1251+26T>G) c.1059+26T>G (n.1059+26T>G) c.950+26T>G c.1209+26T>G (n.1209+26T>G) n.711+26T>G n.825+26T>G c.1017+26T>G (n.1017+26T>G) c.834+26T>G (n.834+26T>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.77933505T= | CA1177626835 | NEXN | c.1251+26T= (n.1251+26T=) c.1059+26T= (n.1059+26T=) c.950+26T= c.1209+26T= (n.1209+26T=) n.711+26T= n.825+26T= c.1017+26T= (n.1017+26T=) c.834+26T= (n.834+26T=) | |
1 | g.77933506C>A | CA918833 | NEXN | c.1251+27C>A (n.1251+27C>A) c.1059+27C>A (n.1059+27C>A) c.950+27C>A c.1209+27C>A (n.1209+27C>A) n.711+27C>A n.825+27C>A c.1017+27C>A (n.1017+27C>A) c.834+27C>A (n.834+27C>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.77933506C= | CA1177626836 | NEXN | c.1251+27C= (n.1251+27C=) c.1059+27C= (n.1059+27C=) c.950+27C= c.1209+27C= (n.1209+27C=) n.711+27C= n.825+27C= c.1017+27C= (n.1017+27C=) c.834+27C= (n.834+27C=) | |
1 | g.77933506C>G | CA24684394 | NEXN | c.1251+27C>G (n.1251+27C>G) c.1059+27C>G (n.1059+27C>G) c.950+27C>G c.1209+27C>G (n.1209+27C>G) n.711+27C>G n.825+27C>G c.1017+27C>G (n.1017+27C>G) c.834+27C>G (n.834+27C>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933506C>T | CA918832 | NEXN | c.1251+27C>T (n.1251+27C>T) c.1059+27C>T (n.1059+27C>T) c.950+27C>T c.1209+27C>T (n.1209+27C>T) n.711+27C>T n.825+27C>T c.1017+27C>T (n.1017+27C>T) c.834+27C>T (n.834+27C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933509del | CA2646274544 | NEXN | c.1251+30del (n.1251+30del) c.1059+30del (n.1059+30del) c.950+30del c.1209+30del (n.1209+30del) n.711+30del n.825+30del c.1017+30del (n.1017+30del) c.834+30del (n.834+30del) | gnomAD v4 |
1 | g.77933507C>A | CA2646274545 | NEXN | c.1251+28C>A (n.1251+28C>A) c.1059+28C>A (n.1059+28C>A) c.950+28C>A c.1209+28C>A (n.1209+28C>A) n.711+28C>A n.825+28C>A c.1017+28C>A (n.1017+28C>A) c.834+28C>A (n.834+28C>A) | gnomAD v4 |
1 | g.77933507C>T | CA2520293314 | NEXN | c.1251+28C>T (n.1251+28C>T) c.1059+28C>T (n.1059+28C>T) c.950+28C>T c.1209+28C>T (n.1209+28C>T) n.711+28C>T n.825+28C>T c.1017+28C>T (n.1017+28C>T) c.834+28C>T (n.834+28C>T) | gnomAD v4 |
1 | g.77933508C>A | CA2535759913 | NEXN | c.1251+29C>A (n.1251+29C>A) c.1059+29C>A (n.1059+29C>A) c.950+29C>A c.1209+29C>A (n.1209+29C>A) n.711+29C>A n.825+29C>A c.1017+29C>A (n.1017+29C>A) c.834+29C>A (n.834+29C>A) | gnomAD v4 |
1 | g.77933508C>T | CA2646274546 | NEXN | c.1251+29C>T (n.1251+29C>T) c.1059+29C>T (n.1059+29C>T) c.950+29C>T c.1209+29C>T (n.1209+29C>T) n.711+29C>T n.825+29C>T c.1017+29C>T (n.1017+29C>T) c.834+29C>T (n.834+29C>T) | gnomAD v4 |
1 | g.77933509C>A | CA2646274547 | NEXN | c.1251+30C>A (n.1251+30C>A) c.1059+30C>A (n.1059+30C>A) c.950+30C>A c.1209+30C>A (n.1209+30C>A) n.711+30C>A n.825+30C>A c.1017+30C>A (n.1017+30C>A) c.834+30C>A (n.834+30C>A) | gnomAD v4 |
1 | g.77933510A>G | CA2646274548 | NEXN | c.1251+31A>G (n.1251+31A>G) c.1059+31A>G (n.1059+31A>G) c.950+31A>G c.1209+31A>G (n.1209+31A>G) n.711+31A>G n.825+31A>G c.1017+31A>G (n.1017+31A>G) c.834+31A>G (n.834+31A>G) | gnomAD v4 |
1 | g.77933511T>A | CA524231123 | NEXN | c.1251+32T>A (n.1251+32T>A) c.1059+32T>A (n.1059+32T>A) c.950+32T>A c.1209+32T>A (n.1209+32T>A) n.711+32T>A n.825+32T>A c.1017+32T>A (n.1017+32T>A) c.834+32T>A (n.834+32T>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933511T= | CA1177626838 | NEXN | c.1251+32T= (n.1251+32T=) c.1059+32T= (n.1059+32T=) c.950+32T= c.1209+32T= (n.1209+32T=) n.711+32T= n.825+32T= c.1017+32T= (n.1017+32T=) c.834+32T= (n.834+32T=) |