Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.77933377del | CA2574414090 | NEXN | c.1149del (p.Lys383AsnfsTer19) c.957del (p.Lys319AsnfsTer19) c.848del c.957del (p.Lys319AsnfsTer?) c.1107del (p.Lys369AsnfsTer19) n.609del n.723del c.915del (p.Lys305AsnfsTer19) c.732del (p.Lys244AsnfsTer19) | |
1 | g.77933378_77933382del | CA2646274521 | NEXN | c.1150_1154del (p.Gln384AsnfsTer15) c.958_962del (p.Gln320AsnfsTer15) c.849_853del c.958_962del (p.Gln320=) c.1108_1112del (p.Gln370AsnfsTer15) n.610_614del n.724_728del c.916_920del (p.Gln306AsnfsTer15) c.733_737del (p.Gln245AsnfsTer15) | gnomAD v4 |
1 | g.77933376A>C | CA340876888 | NEXN | c.1148A>C (p.Lys383Thr) c.956A>C (p.Lys319Thr) c.847A>C c.1106A>C (p.Lys369Thr) n.608A>C n.722A>C c.914A>C (p.Lys305Thr) c.731A>C (p.Lys244Thr) | |
1 | g.77933376A>G | CA340876891 | NEXN | c.1148A>G (p.Lys383Arg) c.956A>G (p.Lys319Arg) c.847A>G c.1106A>G (p.Lys369Arg) n.608A>G n.722A>G c.914A>G (p.Lys305Arg) c.731A>G (p.Lys244Arg) | |
1 | g.77933376A>T | CA340876893 | NEXN | c.1148A>T (p.Lys383Ile) c.956A>T (p.Lys319Ile) c.847A>T c.1106A>T (p.Lys369Ile) n.608A>T n.722A>T c.914A>T (p.Lys305Ile) c.731A>T (p.Lys244Ile) | gnomAD v4 |
1 | g.77933377A= | CA1144428595 | NEXN | c.1149A= (p.Lys383=) c.957A= (p.Lys319=) c.848A= c.1107A= (p.Lys369=) n.609A= n.723A= c.915A= (p.Lys305=) c.732A= (p.Lys244=) | |
1 | g.77933377A>C | CA340876894 | NEXN | c.1149A>C (p.Lys383Asn) c.957A>C (p.Lys319Asn) c.848A>C c.1107A>C (p.Lys369Asn) n.609A>C n.723A>C c.915A>C (p.Lys305Asn) c.732A>C (p.Lys244Asn) | |
1 | g.77933377A>G | CA24684218 | NEXN | c.1149A>G (p.Lys383=) c.957A>G (p.Lys319=) c.848A>G c.1107A>G (p.Lys369=) n.609A>G n.723A>G c.915A>G (p.Lys305=) c.732A>G (p.Lys244=) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.77933377A>T | CA340876897 | NEXN | c.1149A>T (p.Lys383Asn) c.957A>T (p.Lys319Asn) c.848A>T c.1107A>T (p.Lys369Asn) n.609A>T n.723A>T c.915A>T (p.Lys305Asn) c.732A>T (p.Lys244Asn) | |
1 | g.77933378C>A | CA340876899 | NEXN | c.1150C>A (p.Gln384Lys) c.958C>A (p.Gln320Lys) c.849C>A c.1108C>A (p.Gln370Lys) n.610C>A n.724C>A c.916C>A (p.Gln306Lys) c.733C>A (p.Gln245Lys) | gnomAD v3 gnomAD v4 |
1 | g.77933378C= | CA1177626734 | NEXN | c.1150C= (p.Gln384=) c.958C= (p.Gln320=) c.849C= c.1108C= (p.Gln370=) n.610C= n.724C= c.916C= (p.Gln306=) c.733C= (p.Gln245=) | |
1 | g.77933378C>G | CA340876901 | NEXN | c.1150C>G (p.Gln384Glu) c.958C>G (p.Gln320Glu) c.849C>G c.1108C>G (p.Gln370Glu) n.610C>G n.724C>G c.916C>G (p.Gln306Glu) c.733C>G (p.Gln245Glu) | dbSNP gnomAD v4 |
1 | g.77933378C>T | CA340876902 | NEXN | c.1150C>T (p.Gln384Ter) c.958C>T (p.Gln320Ter) c.849C>T c.1108C>T (p.Gln370Ter) n.610C>T n.724C>T c.916C>T (p.Gln306Ter) c.733C>T (p.Gln245Ter) | |
1 | g.77933379A= | CA1177626735 | NEXN | c.1151A= (p.Gln384=) c.959A= (p.Gln320=) c.850A= c.1109A= (p.Gln370=) n.611A= n.725A= c.917A= (p.Gln306=) c.734A= (p.Gln245=) | |
1 | g.77933379A>C | CA340876904 | NEXN | c.1151A>C (p.Gln384Pro) c.959A>C (p.Gln320Pro) c.850A>C c.1109A>C (p.Gln370Pro) n.611A>C n.725A>C c.917A>C (p.Gln306Pro) c.734A>C (p.Gln245Pro) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933379A>G | CA340876906 | NEXN | c.1151A>G (p.Gln384Arg) c.959A>G (p.Gln320Arg) c.850A>G c.1109A>G (p.Gln370Arg) n.611A>G n.725A>G c.917A>G (p.Gln306Arg) c.734A>G (p.Gln245Arg) | |
1 | g.77933379A>T | CA340876907 | NEXN | c.1151A>T (p.Gln384Leu) c.959A>T (p.Gln320Leu) c.850A>T c.1109A>T (p.Gln370Leu) n.611A>T n.725A>T c.917A>T (p.Gln306Leu) c.734A>T (p.Gln245Leu) | |
1 | g.77933384dup | CA658762962 | NEXN | c.1156dup (p.Met386AsnfsTer15) c.964dup (p.Met322AsnfsTer15) c.855dup c.1114dup (p.Met372AsnfsTer15) n.616dup n.730dup c.922dup (p.Met308AsnfsTer15) c.739dup (p.Met247AsnfsTer15) | |
1 | g.77933380A>C | CA340876911 | NEXN | c.1152A>C (p.Gln384His) c.960A>C (p.Gln320His) c.851A>C c.1110A>C (p.Gln370His) n.612A>C n.726A>C c.918A>C (p.Gln306His) c.735A>C (p.Gln245His) | |
1 | g.77933380A>G | CA418572084 | NEXN | c.1152A>G (p.Gln384=) c.960A>G (p.Gln320=) c.851A>G c.1110A>G (p.Gln370=) n.612A>G n.726A>G c.918A>G (p.Gln306=) c.735A>G (p.Gln245=) | |
1 | g.77933380A>T | CA340876909 | NEXN | c.1152A>T (p.Gln384His) c.960A>T (p.Gln320His) c.851A>T c.1110A>T (p.Gln370His) n.612A>T n.726A>T c.918A>T (p.Gln306His) c.735A>T (p.Gln245His) | |
1 | g.77933381A>C | CA340876913 | NEXN | c.1153A>C (p.Lys385Gln) c.961A>C (p.Lys321Gln) c.852A>C c.1111A>C (p.Lys371Gln) n.613A>C n.727A>C c.919A>C (p.Lys307Gln) c.736A>C (p.Lys246Gln) | |
1 | g.77933381A>G | CA340876918 | NEXN | c.1153A>G (p.Lys385Glu) c.961A>G (p.Lys321Glu) c.852A>G c.1111A>G (p.Lys371Glu) n.613A>G n.727A>G c.919A>G (p.Lys307Glu) c.736A>G (p.Lys246Glu) | |
1 | g.77933381A>T | CA340876916 | NEXN | c.1153A>T (p.Lys385Ter) c.961A>T (p.Lys321Ter) c.852A>T c.1111A>T (p.Lys371Ter) n.613A>T n.727A>T c.919A>T (p.Lys307Ter) c.736A>T (p.Lys246Ter) | |
1 | g.77933382A>C | CA340876919 | NEXN | c.1154A>C (p.Lys385Thr) c.962A>C (p.Lys321Thr) c.853A>C c.1112A>C (p.Lys371Thr) n.614A>C n.728A>C c.920A>C (p.Lys307Thr) c.737A>C (p.Lys246Thr) | |
1 | g.77933382A>G | CA340876920 | NEXN | c.1154A>G (p.Lys385Arg) c.962A>G (p.Lys321Arg) c.853A>G c.1112A>G (p.Lys371Arg) n.614A>G n.728A>G c.920A>G (p.Lys307Arg) c.737A>G (p.Lys246Arg) | |
1 | g.77933382A>T | CA340876922 | NEXN | c.1154A>T (p.Lys385Ile) c.962A>T (p.Lys321Ile) c.853A>T c.1112A>T (p.Lys371Ile) n.614A>T n.728A>T c.920A>T (p.Lys307Ile) c.737A>T (p.Lys246Ile) | |
1 | g.77933383A>C | CA340876925 | NEXN | c.1155A>C (p.Lys385Asn) c.963A>C (p.Lys321Asn) c.854A>C c.1113A>C (p.Lys371Asn) n.615A>C n.729A>C c.921A>C (p.Lys307Asn) c.738A>C (p.Lys246Asn) | |
1 | g.77933383A>G | CA418572085 | NEXN | c.1155A>G (p.Lys385=) c.963A>G (p.Lys321=) c.854A>G c.1113A>G (p.Lys371=) n.615A>G n.729A>G c.921A>G (p.Lys307=) c.738A>G (p.Lys246=) | |
1 | g.77933383A>T | CA340876926 | NEXN | c.1155A>T (p.Lys385Asn) c.963A>T (p.Lys321Asn) c.854A>T c.1113A>T (p.Lys371Asn) n.615A>T n.729A>T c.921A>T (p.Lys307Asn) c.738A>T (p.Lys246Asn) | |
1 | g.77933384A>C | CA340876932 | NEXN | c.1156A>C (p.Met386Leu) c.964A>C (p.Met322Leu) c.855A>C c.964A>C c.1114A>C (p.Met372Leu) n.616A>C n.730A>C c.922A>C (p.Met308Leu) c.739A>C (p.Met247Leu) | |
1 | g.77933384A>G | CA340876930 | NEXN | c.1156A>G (p.Met386Val) c.964A>G (p.Met322Val) c.855A>G c.964A>G c.1114A>G (p.Met372Val) n.616A>G n.730A>G c.922A>G (p.Met308Val) c.739A>G (p.Met247Val) | |
1 | g.77933384A>T | CA340876929 | NEXN | c.1156A>T (p.Met386Leu) c.964A>T (p.Met322Leu) c.855A>T c.964A>T c.1114A>T (p.Met372Leu) n.616A>T n.730A>T c.922A>T (p.Met308Leu) c.739A>T (p.Met247Leu) | |
1 | g.77933385T>A | CA340876935 | NEXN | c.1157T>A (p.Met386Lys) c.965T>A (p.Met322Lys) c.856T>A c.1115T>A (p.Met372Lys) n.617T>A n.731T>A c.923T>A (p.Met308Lys) c.740T>A (p.Met247Lys) | |
1 | g.77933385T>C | CA340876936 | NEXN | c.1157T>C (p.Met386Thr) c.965T>C (p.Met322Thr) c.856T>C c.1115T>C (p.Met372Thr) n.617T>C n.731T>C c.923T>C (p.Met308Thr) c.740T>C (p.Met247Thr) | |
1 | g.77933385T>G | CA340876938 | NEXN | c.1157T>G (p.Met386Arg) c.965T>G (p.Met322Arg) c.856T>G c.1115T>G (p.Met372Arg) n.617T>G n.731T>G c.923T>G (p.Met308Arg) c.740T>G (p.Met247Arg) | |
1 | g.77933385_77933390del | CA2744232064 | NEXN | c.1157_1162del (p.Met386_Glu388delinsLys) c.965_970del (p.Met322_Glu324delinsLys) c.856_861del c.1115_1120del (p.Met372_Glu374delinsLys) n.617_622del n.731_736del c.923_928del (p.Met308_Glu310delinsLys) c.740_745del (p.Met247_Glu249delinsLys) | |
1 | g.77933386G>A | CA340876939 | NEXN | c.1158G>A (p.Met386Ile) c.966G>A (p.Met322Ile) c.857G>A c.1116G>A (p.Met372Ile) n.618G>A n.732G>A c.924G>A (p.Met308Ile) c.741G>A (p.Met247Ile) | |
1 | g.77933386G>C | CA340876940 | NEXN | c.1158G>C (p.Met386Ile) c.966G>C (p.Met322Ile) c.857G>C c.1116G>C (p.Met372Ile) n.618G>C n.732G>C c.924G>C (p.Met308Ile) c.741G>C (p.Met247Ile) | gnomAD v4 |
1 | g.77933386G>T | CA340876943 | NEXN | c.1158G>T (p.Met386Ile) c.966G>T (p.Met322Ile) c.857G>T c.1116G>T (p.Met372Ile) n.618G>T n.732G>T c.924G>T (p.Met308Ile) c.741G>T (p.Met247Ile) | |
1 | g.77933386_77933389delinsGGAA | CA1177626736 | NEXN | c.1158_1161delinsGGAA (p.Met386=) c.966_969delinsGGAA (p.Met322=) c.857_860delinsGGAA c.1116_1119delinsGGAA (p.Met372=) n.618_621delinsGGAA n.732_735delinsGGAA c.924_927delinsGGAA (p.Met308=) c.741_744delinsGGAA (p.Met247=) | |
1 | g.77933387G>A | CA340876945 | NEXN | c.1159G>A (p.Glu387Lys) c.967G>A (p.Glu323Lys) c.858G>A c.1117G>A (p.Glu373Lys) n.619G>A n.733G>A c.925G>A (p.Glu309Lys) c.742G>A (p.Glu248Lys) | |
1 | g.77933387G>C | CA340876948 | NEXN | c.1159G>C (p.Glu387Gln) c.967G>C (p.Glu323Gln) c.858G>C c.1117G>C (p.Glu373Gln) n.619G>C n.733G>C c.925G>C (p.Glu309Gln) c.742G>C (p.Glu248Gln) | |
1 | g.77933387G>T | CA340876946 | NEXN | c.1159G>T (p.Glu387Ter) c.967G>T (p.Glu323Ter) c.858G>T c.1117G>T (p.Glu373Ter) n.619G>T n.733G>T c.925G>T (p.Glu309Ter) c.742G>T (p.Glu248Ter) | gnomAD v4 |
1 | g.77933393_77933395del | CA739053276 | NEXN | c.1165_1167del (p.Glu389del) c.973_975del (p.Glu325del) c.864_866del c.1123_1125del (p.Glu375del) n.625_627del n.739_741del c.931_933del (p.Glu311del) c.748_750del (p.Glu250del) | dbSNP gnomAD v4 |
1 | g.77933388A>C | CA340876950 | NEXN | c.1160A>C (p.Glu387Ala) c.968A>C (p.Glu323Ala) c.859A>C c.1118A>C (p.Glu373Ala) n.620A>C n.734A>C c.926A>C (p.Glu309Ala) c.743A>C (p.Glu248Ala) | |
1 | g.77933388A>G | CA340876951 | NEXN | c.1160A>G (p.Glu387Gly) c.968A>G (p.Glu323Gly) c.859A>G c.1118A>G (p.Glu373Gly) n.620A>G n.734A>G c.926A>G (p.Glu309Gly) c.743A>G (p.Glu248Gly) | |
1 | g.77933388A>T | CA340876953 | NEXN | c.1160A>T (p.Glu387Val) c.968A>T (p.Glu323Val) c.859A>T c.1118A>T (p.Glu373Val) n.620A>T n.734A>T c.926A>T (p.Glu309Val) c.743A>T (p.Glu248Val) | |
1 | g.77933389A>C | CA340876954 | NEXN | c.1161A>C (p.Glu387Asp) c.969A>C (p.Glu323Asp) c.860A>C c.1119A>C (p.Glu373Asp) n.621A>C n.735A>C c.927A>C (p.Glu309Asp) c.744A>C (p.Glu248Asp) | |
1 | g.77933389A>G | CA418572086 | NEXN | c.1161A>G (p.Glu387=) c.969A>G (p.Glu323=) c.860A>G c.1119A>G (p.Glu373=) n.621A>G n.735A>G c.927A>G (p.Glu309=) c.744A>G (p.Glu248=) | |
1 | g.77933389A>T | CA340876956 | NEXN | c.1161A>T (p.Glu387Asp) c.969A>T (p.Glu323Asp) c.860A>T c.1119A>T (p.Glu373Asp) n.621A>T n.735A>T c.927A>T (p.Glu309Asp) c.744A>T (p.Glu248Asp) | |
1 | g.77933390G>A | CA340876958 | NEXN | c.1162G>A (p.Glu388Lys) c.970G>A (p.Glu324Lys) c.861G>A c.1120G>A (p.Glu374Lys) n.622G>A n.736G>A c.928G>A (p.Glu310Lys) c.745G>A (p.Glu249Lys) | ClinVar gnomAD v4 COSMIC COSMIC |
1 | g.77933390G>C | CA340876959 | NEXN | c.1162G>C (p.Glu388Gln) c.970G>C (p.Glu324Gln) c.861G>C c.1120G>C (p.Glu374Gln) n.622G>C n.736G>C c.928G>C (p.Glu310Gln) c.745G>C (p.Glu249Gln) | COSMIC COSMIC |
1 | g.77933390G= | CA1177626737 | NEXN | c.1162G= (p.Glu388=) c.970G= (p.Glu324=) c.861G= c.1120G= (p.Glu374=) n.622G= n.736G= c.928G= (p.Glu310=) c.745G= (p.Glu249=) | |
1 | g.77933390G>T | CA918808 | NEXN | c.1162G>T (p.Glu388Ter) c.970G>T (p.Glu324Ter) c.861G>T c.1120G>T (p.Glu374Ter) n.622G>T n.736G>T c.928G>T (p.Glu310Ter) c.745G>T (p.Glu249Ter) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.77933391A= | CA1177626738 | NEXN | c.1163A= (p.Glu388=) c.971A= (p.Glu324=) c.862A= c.1121A= (p.Glu374=) n.623A= n.737A= c.929A= (p.Glu310=) c.746A= (p.Glu249=) | |
1 | g.77933391A>C | CA340876962 | NEXN | c.1163A>C (p.Glu388Ala) c.971A>C (p.Glu324Ala) c.862A>C c.1121A>C (p.Glu374Ala) n.623A>C n.737A>C c.929A>C (p.Glu310Ala) c.746A>C (p.Glu249Ala) | |
1 | g.77933391A>G | CA918809 | NEXN | c.1163A>G (p.Glu388Gly) c.971A>G (p.Glu324Gly) c.862A>G c.1121A>G (p.Glu374Gly) n.623A>G n.737A>G c.929A>G (p.Glu310Gly) c.746A>G (p.Glu249Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.77933391A>T | CA340876965 | NEXN | c.1163A>T (p.Glu388Val) c.971A>T (p.Glu324Val) c.862A>T c.1121A>T (p.Glu374Val) n.623A>T n.737A>T c.929A>T (p.Glu310Val) c.746A>T (p.Glu249Val) | |
1 | g.77933392A>C | CA340876967 | NEXN | c.1164A>C (p.Glu388Asp) c.972A>C (p.Glu324Asp) c.863A>C c.1122A>C (p.Glu374Asp) n.624A>C n.738A>C c.930A>C (p.Glu310Asp) c.747A>C (p.Glu249Asp) | |
1 | g.77933392A>G | CA418572087 | NEXN | c.1164A>G (p.Glu388=) c.972A>G (p.Glu324=) c.863A>G c.1122A>G (p.Glu374=) n.624A>G n.738A>G c.930A>G (p.Glu310=) c.747A>G (p.Glu249=) | |
1 | g.77933392A>T | CA340876968 | NEXN | c.1164A>T (p.Glu388Asp) c.972A>T (p.Glu324Asp) c.863A>T c.1122A>T (p.Glu374Asp) n.624A>T n.738A>T c.930A>T (p.Glu310Asp) c.747A>T (p.Glu249Asp) | |
1 | g.77933393G>A | CA340876970 | NEXN | c.1165G>A (p.Glu389Lys) c.973G>A (p.Glu325Lys) c.864G>A c.1123G>A (p.Glu375Lys) n.625G>A n.739G>A c.931G>A (p.Glu311Lys) c.748G>A (p.Glu250Lys) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.77933393G>C | CA340876972 | NEXN | c.1165G>C (p.Glu389Gln) c.973G>C (p.Glu325Gln) c.864G>C c.1123G>C (p.Glu375Gln) n.625G>C n.739G>C c.931G>C (p.Glu311Gln) c.748G>C (p.Glu250Gln) | gnomAD v4 |
1 | g.77933393G= | CA1177626739 | NEXN | c.1165G= (p.Glu389=) c.973G= (p.Glu325=) c.864G= c.1123G= (p.Glu375=) n.625G= n.739G= c.931G= (p.Glu311=) c.748G= (p.Glu250=) | |
1 | g.77933393G>T | CA340876973 | NEXN | c.1165G>T (p.Glu389Ter) c.973G>T (p.Glu325Ter) c.864G>T c.1123G>T (p.Glu375Ter) n.625G>T n.739G>T c.931G>T (p.Glu311Ter) c.748G>T (p.Glu250Ter) | |
1 | g.77933394A>C | CA340876975 | NEXN | c.1166A>C (p.Glu389Ala) c.974A>C (p.Glu325Ala) c.865A>C c.1124A>C (p.Glu375Ala) n.626A>C n.740A>C c.932A>C (p.Glu311Ala) c.749A>C (p.Glu250Ala) | |
1 | g.77933394A>G | CA340876976 | NEXN | c.1166A>G (p.Glu389Gly) c.974A>G (p.Glu325Gly) c.865A>G c.1124A>G (p.Glu375Gly) n.626A>G n.740A>G c.932A>G (p.Glu311Gly) c.749A>G (p.Glu250Gly) | |
1 | g.77933394A>T | CA340876978 | NEXN | c.1166A>T (p.Glu389Val) c.974A>T (p.Glu325Val) c.865A>T c.1124A>T (p.Glu375Val) n.626A>T n.740A>T c.932A>T (p.Glu311Val) c.749A>T (p.Glu250Val) | |
1 | g.77933398del | CA2580063259 | NEXN | c.1170del (p.Lys390AsnfsTer12) c.978del (p.Lys326AsnfsTer12) c.869del c.1128del (p.Lys376AsnfsTer12) n.630del n.744del c.936del (p.Lys312AsnfsTer12) c.753del (p.Lys251AsnfsTer12) | ClinVar gnomAD v4 |
1 | g.77933395A>C | CA340876979 | NEXN | c.1167A>C (p.Glu389Asp) c.975A>C (p.Glu325Asp) c.866A>C c.1125A>C (p.Glu375Asp) n.627A>C n.741A>C c.933A>C (p.Glu311Asp) c.750A>C (p.Glu250Asp) | |
1 | g.77933395A>G | CA418572088 | NEXN | c.1167A>G (p.Glu389=) c.975A>G (p.Glu325=) c.866A>G c.1125A>G (p.Glu375=) n.627A>G n.741A>G c.933A>G (p.Glu311=) c.750A>G (p.Glu250=) | |
1 | g.77933395A>T | CA340876981 | NEXN | c.1167A>T (p.Glu389Asp) c.975A>T (p.Glu325Asp) c.866A>T c.1125A>T (p.Glu375Asp) n.627A>T n.741A>T c.933A>T (p.Glu311Asp) c.750A>T (p.Glu250Asp) | |
1 | g.77933396A>C | CA340876982 | NEXN | c.1168A>C (p.Lys390Gln) c.976A>C (p.Lys326Gln) c.867A>C c.1126A>C (p.Lys376Gln) n.628A>C n.742A>C c.934A>C (p.Lys312Gln) c.751A>C (p.Lys251Gln) | |
1 | g.77933396A>G | CA340876983 | NEXN | c.1168A>G (p.Lys390Glu) c.976A>G (p.Lys326Glu) c.867A>G c.1126A>G (p.Lys376Glu) n.628A>G n.742A>G c.934A>G (p.Lys312Glu) c.751A>G (p.Lys251Glu) | gnomAD v4 |
1 | g.77933396A>T | CA340876985 | NEXN | c.1168A>T (p.Lys390Ter) c.976A>T (p.Lys326Ter) c.867A>T c.1126A>T (p.Lys376Ter) n.628A>T n.742A>T c.934A>T (p.Lys312Ter) c.751A>T (p.Lys251Ter) | |
1 | g.77933397A>C | CA340876987 | NEXN | c.1169A>C (p.Lys390Thr) c.977A>C (p.Lys326Thr) c.868A>C c.1127A>C (p.Lys376Thr) n.629A>C n.743A>C c.935A>C (p.Lys312Thr) c.752A>C (p.Lys251Thr) | ClinVar gnomAD v4 |
1 | g.77933397A>G | CA340876989 | NEXN | c.1169A>G (p.Lys390Arg) c.977A>G (p.Lys326Arg) c.868A>G c.1127A>G (p.Lys376Arg) n.629A>G n.743A>G c.935A>G (p.Lys312Arg) c.752A>G (p.Lys251Arg) | |
1 | g.77933397A>T | CA340876990 | NEXN | c.1169A>T (p.Lys390Ile) c.977A>T (p.Lys326Ile) c.868A>T c.1127A>T (p.Lys376Ile) n.629A>T n.743A>T c.935A>T (p.Lys312Ile) c.752A>T (p.Lys251Ile) | |
1 | g.77933397_77933398insCGATA | CA2646274522 | NEXN | c.1169_1170insCGATA (p.Lys390AsnfsTer14) c.977_978insCGATA (p.Lys326AsnfsTer14) c.868_869insCGATA c.1127_1128insCGATA (p.Lys376AsnfsTer14) n.629_630insCGATA n.743_744insCGATA c.935_936insCGATA (p.Lys312AsnfsTer14) c.752_753insCGATA (p.Lys251AsnfsTer14) | gnomAD v4 |
1 | g.77933398A>C | CA340876994 | NEXN | c.1170A>C (p.Lys390Asn) c.978A>C (p.Lys326Asn) c.869A>C c.1128A>C (p.Lys376Asn) n.630A>C n.744A>C c.936A>C (p.Lys312Asn) c.753A>C (p.Lys251Asn) | |
1 | g.77933398A>G | CA418572089 | NEXN | c.1170A>G (p.Lys390=) c.978A>G (p.Lys326=) c.869A>G c.1128A>G (p.Lys376=) n.630A>G n.744A>G c.936A>G (p.Lys312=) c.753A>G (p.Lys251=) | |
1 | g.77933398A>T | CA340876992 | NEXN | c.1170A>T (p.Lys390Asn) c.978A>T (p.Lys326Asn) c.869A>T c.1128A>T (p.Lys376Asn) n.630A>T n.744A>T c.936A>T (p.Lys312Asn) c.753A>T (p.Lys251Asn) | |
1 | g.77933399C>A | CA418572090 | NEXN | c.1171C>A (p.Arg391=) c.979C>A (p.Arg327=) c.870C>A c.1129C>A (p.Arg377=) n.631C>A n.745C>A c.937C>A (p.Arg313=) c.754C>A (p.Arg252=) | |
1 | g.77933399C= | CA1143395136 | NEXN | c.1171C= (p.Arg391=) c.979C= (p.Arg327=) c.870C= c.1129C= (p.Arg377=) n.631C= n.745C= c.937C= (p.Arg313=) c.754C= (p.Arg252=) | |
1 | g.77933399C>G | CA340876996 | NEXN | c.1171C>G (p.Arg391Gly) c.979C>G (p.Arg327Gly) c.870C>G c.1129C>G (p.Arg377Gly) n.631C>G n.745C>G c.937C>G (p.Arg313Gly) c.754C>G (p.Arg252Gly) | ClinVar gnomAD v4 |
1 | g.77933399C>T | CA918810 | NEXN | c.1171C>T (p.Arg391Ter) c.979C>T (p.Arg327Ter) c.870C>T c.1129C>T (p.Arg377Ter) n.631C>T n.745C>T c.937C>T (p.Arg313Ter) c.754C>T (p.Arg252Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933400G>A | CA918811 | NEXN | c.1172G>A (p.Arg391Gln) c.980G>A (p.Arg327Gln) c.871G>A c.1130G>A (p.Arg377Gln) n.632G>A n.746G>A c.938G>A (p.Arg313Gln) c.755G>A (p.Arg252Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933400G>C | CA340876998 | NEXN | c.1172G>C (p.Arg391Pro) c.980G>C (p.Arg327Pro) c.871G>C c.1130G>C (p.Arg377Pro) n.632G>C n.746G>C c.938G>C (p.Arg313Pro) c.755G>C (p.Arg252Pro) | |
1 | g.77933400G= | CA1177626740 | NEXN | c.1172G= (p.Arg391=) c.980G= (p.Arg327=) c.871G= c.1130G= (p.Arg377=) n.632G= n.746G= c.938G= (p.Arg313=) c.755G= (p.Arg252=) | |
1 | g.77933400G>T | CA340876999 | NEXN | c.1172G>T (p.Arg391Leu) c.980G>T (p.Arg327Leu) c.871G>T c.1130G>T (p.Arg377Leu) n.632G>T n.746G>T c.938G>T (p.Arg313Leu) c.755G>T (p.Arg252Leu) | |
1 | g.77933401A>C | CA418572091 | NEXN | c.1173A>C (p.Arg391=) c.981A>C (p.Arg327=) c.872A>C c.1131A>C (p.Arg377=) n.633A>C n.747A>C c.939A>C (p.Arg313=) c.756A>C (p.Arg252=) | |
1 | g.77933401A>G | CA418572093 | NEXN | c.1173A>G (p.Arg391=) c.981A>G (p.Arg327=) c.872A>G c.1131A>G (p.Arg377=) n.633A>G n.747A>G c.939A>G (p.Arg313=) c.756A>G (p.Arg252=) | |
1 | g.77933401A>T | CA418572092 | NEXN | c.1173A>T (p.Arg391=) c.981A>T (p.Arg327=) c.872A>T c.1131A>T (p.Arg377=) n.633A>T n.747A>T c.939A>T (p.Arg313=) c.756A>T (p.Arg252=) | |
1 | g.77933402C>A | CA418572094 | NEXN | c.1174C>A (p.Arg392=) c.982C>A (p.Arg328=) c.873C>A c.1132C>A (p.Arg378=) n.634C>A n.748C>A c.940C>A (p.Arg314=) c.757C>A (p.Arg253=) | |
1 | g.77933402C= | CA1177626741 | NEXN | c.1174C= (p.Arg392=) c.982C= (p.Arg328=) c.873C= c.1132C= (p.Arg378=) n.634C= n.748C= c.940C= (p.Arg314=) c.757C= (p.Arg253=) | |
1 | g.77933402C>G | CA340877001 | NEXN | c.1174C>G (p.Arg392Gly) c.982C>G (p.Arg328Gly) c.873C>G c.1132C>G (p.Arg378Gly) n.634C>G n.748C>G c.940C>G (p.Arg314Gly) c.757C>G (p.Arg253Gly) | |
1 | g.77933402C>T | CA918812 | NEXN | c.1174C>T (p.Arg392Ter) c.982C>T (p.Arg328Ter) c.873C>T c.1132C>T (p.Arg378Ter) n.634C>T n.748C>T c.940C>T (p.Arg314Ter) c.757C>T (p.Arg253Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933403G>A | CA24684248 | NEXN | c.1175G>A (p.Arg392Gln) c.983G>A (p.Arg328Gln) c.874G>A c.1133G>A (p.Arg378Gln) n.635G>A n.749G>A c.941G>A (p.Arg314Gln) c.758G>A (p.Arg253Gln) | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
1 | g.77933403G>C | CA340877004 | NEXN | c.1175G>C (p.Arg392Pro) c.983G>C (p.Arg328Pro) c.874G>C c.1133G>C (p.Arg378Pro) n.635G>C n.749G>C c.941G>C (p.Arg314Pro) c.758G>C (p.Arg253Pro) | ClinVar dbSNP |
1 | g.77933403G= | CA1177626742 | NEXN | c.1175G= (p.Arg392=) c.983G= (p.Arg328=) c.874G= c.1133G= (p.Arg378=) n.635G= n.749G= c.941G= (p.Arg314=) c.758G= (p.Arg253=) | |
1 | g.77933403G>T | CA340877005 | NEXN | c.1175G>T (p.Arg392Leu) c.983G>T (p.Arg328Leu) c.874G>T c.1133G>T (p.Arg378Leu) n.635G>T n.749G>T c.941G>T (p.Arg314Leu) c.758G>T (p.Arg253Leu) | ClinVar dbSNP gnomAD v4 |
1 | g.77933404A>C | CA418572095 | NEXN | c.1176A>C (p.Arg392=) c.984A>C (p.Arg328=) c.875A>C c.1134A>C (p.Arg378=) n.636A>C n.750A>C c.942A>C (p.Arg314=) c.759A>C (p.Arg253=) | |
1 | g.77933404A>G | CA418572096 | NEXN | c.1176A>G (p.Arg392=) c.984A>G (p.Arg328=) c.875A>G c.1134A>G (p.Arg378=) n.636A>G n.750A>G c.942A>G (p.Arg314=) c.759A>G (p.Arg253=) | |
1 | g.77933404A>T | CA418572097 | NEXN | c.1176A>T (p.Arg392=) c.984A>T (p.Arg328=) c.875A>T c.1134A>T (p.Arg378=) n.636A>T n.750A>T c.942A>T (p.Arg314=) c.759A>T (p.Arg253=) | |
1 | g.77933405A= | CA1177626745 | NEXN | c.1177A= (p.Thr393=) c.985A= (p.Thr329=) c.876A= c.1135A= (p.Thr379=) n.637A= n.751A= c.943A= (p.Thr315=) c.760A= (p.Thr254=) | |
1 | g.77933405A>C | CA340877006 | NEXN | c.1177A>C (p.Thr393Pro) c.985A>C (p.Thr329Pro) c.876A>C c.1135A>C (p.Thr379Pro) n.637A>C n.751A>C c.943A>C (p.Thr315Pro) c.760A>C (p.Thr254Pro) | |
1 | g.77933405A>G | CA340877007 | NEXN | c.1177A>G (p.Thr393Ala) c.985A>G (p.Thr329Ala) c.876A>G c.1135A>G (p.Thr379Ala) n.637A>G n.751A>G c.943A>G (p.Thr315Ala) c.760A>G (p.Thr254Ala) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.77933405A>T | CA340877008 | NEXN | c.1177A>T (p.Thr393Ser) c.985A>T (p.Thr329Ser) c.876A>T c.1135A>T (p.Thr379Ser) n.637A>T n.751A>T c.943A>T (p.Thr315Ser) c.760A>T (p.Thr254Ser) | |
1 | g.77933406C>A | CA340877012 | NEXN | c.1178C>A (p.Thr393Lys) c.986C>A (p.Thr329Lys) c.877C>A c.1136C>A (p.Thr379Lys) n.638C>A n.752C>A c.944C>A (p.Thr315Lys) c.761C>A (p.Thr254Lys) | gnomAD v4 |
1 | g.77933406C>G | CA340877011 | NEXN | c.1178C>G (p.Thr393Arg) c.986C>G (p.Thr329Arg) c.877C>G c.1136C>G (p.Thr379Arg) n.638C>G n.752C>G c.944C>G (p.Thr315Arg) c.761C>G (p.Thr254Arg) | |
1 | g.77933406C>T | CA340877009 | NEXN | c.1178C>T (p.Thr393Ile) c.986C>T (p.Thr329Ile) c.877C>T c.1136C>T (p.Thr379Ile) n.638C>T n.752C>T c.944C>T (p.Thr315Ile) c.761C>T (p.Thr254Ile) | |
1 | g.77933406_77933408delinsCAG | CA1177626746 | NEXN | c.1178_1180delinsCAG (p.Thr393=) c.986_988delinsCAG (p.Thr329=) c.877_879delinsCAG c.1136_1138delinsCAG (p.Thr379=) n.638_640delinsCAG n.752_754delinsCAG c.944_946delinsCAG (p.Thr315=) c.761_763delinsCAG (p.Thr254=) | |
1 | g.77933407A= | CA1177626749 | NEXN | c.1179A= (p.Thr393=) c.987A= (p.Thr329=) c.878A= c.1137A= (p.Thr379=) n.639A= n.753A= c.945A= (p.Thr315=) c.762A= (p.Thr254=) | |
1 | g.77933407A>C | CA418572098 | NEXN | c.1179A>C (p.Thr393=) c.987A>C (p.Thr329=) c.878A>C c.1137A>C (p.Thr379=) n.639A>C n.753A>C c.945A>C (p.Thr315=) c.762A>C (p.Thr254=) | ClinVar dbSNP gnomAD v4 |
1 | g.77933407A>G | CA418572099 | NEXN | c.1179A>G (p.Thr393=) c.987A>G (p.Thr329=) c.878A>G c.1137A>G (p.Thr379=) n.639A>G n.753A>G c.945A>G (p.Thr315=) c.762A>G (p.Thr254=) | dbSNP |
1 | g.77933407A>T | CA418572100 | NEXN | c.1179A>T (p.Thr393=) c.987A>T (p.Thr329=) c.878A>T c.1137A>T (p.Thr379=) n.639A>T n.753A>T c.945A>T (p.Thr315=) c.762A>T (p.Thr254=) | |
1 | g.77933407_77933410delinsAGAG | CA1148224376 | NEXN | c.1179_1182delinsAGAG (p.Thr393=) c.987_990delinsAGAG (p.Thr329=) c.878_881delinsAGAG c.1137_1140delinsAGAG (p.Thr379=) n.639_642delinsAGAG n.753_756delinsAGAG c.945_948delinsAGAG (p.Thr315=) c.762_765delinsAGAG (p.Thr254=) | |
1 | g.77933409_77933410del | CA184438 | NEXN | c.1181_1182del (p.Glu394GlyfsTer6) c.989_990del (p.Glu330GlyfsTer6) c.880_881del c.1139_1140del (p.Glu380GlyfsTer6) n.641_642del n.755_756del c.947_948del (p.Glu316GlyfsTer6) c.764_765del (p.Glu255GlyfsTer6) | ClinVar dbSNP |
1 | g.77933408G>A | CA340877015 | NEXN | c.1180G>A (p.Glu394Lys) c.988G>A (p.Glu330Lys) c.879G>A c.1138G>A (p.Glu380Lys) n.640G>A n.754G>A c.946G>A (p.Glu316Lys) c.763G>A (p.Glu255Lys) | gnomAD v4 |
1 | g.77933408G>C | CA340877018 | NEXN | c.1180G>C (p.Glu394Gln) c.988G>C (p.Glu330Gln) c.879G>C c.1138G>C (p.Glu380Gln) n.640G>C n.754G>C c.946G>C (p.Glu316Gln) c.763G>C (p.Glu255Gln) | |
1 | g.77933408G>T | CA340877016 | NEXN | c.1180G>T (p.Glu394Ter) c.988G>T (p.Glu330Ter) c.879G>T c.1138G>T (p.Glu380Ter) n.640G>T n.754G>T c.946G>T (p.Glu316Ter) c.763G>T (p.Glu255Ter) | |
1 | g.77933409A>C | CA340877020 | NEXN | c.1181A>C (p.Glu394Ala) c.989A>C (p.Glu330Ala) c.880A>C c.1139A>C (p.Glu380Ala) n.641A>C n.755A>C c.947A>C (p.Glu316Ala) c.764A>C (p.Glu255Ala) | |
1 | g.77933409A>G | CA340877022 | NEXN | c.1181A>G (p.Glu394Gly) c.989A>G (p.Glu330Gly) c.880A>G c.1139A>G (p.Glu380Gly) n.641A>G n.755A>G c.947A>G (p.Glu316Gly) c.764A>G (p.Glu255Gly) | |
1 | g.77933409A>T | CA340877024 | NEXN | c.1181A>T (p.Glu394Val) c.989A>T (p.Glu330Val) c.880A>T c.1139A>T (p.Glu380Val) n.641A>T n.755A>T c.947A>T (p.Glu316Val) c.764A>T (p.Glu255Val) | |
1 | g.77933410G>A | CA418572101 | NEXN | c.1182G>A (p.Glu394=) c.990G>A (p.Glu330=) c.881G>A c.1140G>A (p.Glu380=) n.642G>A n.756G>A c.948G>A (p.Glu316=) c.765G>A (p.Glu255=) | ClinVar gnomAD v4 |
1 | g.77933410G>C | CA340877028 | NEXN | c.1182G>C (p.Glu394Asp) c.990G>C (p.Glu330Asp) c.881G>C c.1140G>C (p.Glu380Asp) n.642G>C n.756G>C c.948G>C (p.Glu316Asp) c.765G>C (p.Glu255Asp) | |
1 | g.77933410G>T | CA340877026 | NEXN | c.1182G>T (p.Glu394Asp) c.990G>T (p.Glu330Asp) c.881G>T c.1140G>T (p.Glu380Asp) n.642G>T n.756G>T c.948G>T (p.Glu316Asp) c.765G>T (p.Glu255Asp) | |
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=) |