Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.77933279T>C | CA2646274517 | NEXN | c.1054-3T>C (n.1054-3T>C) c.862-3T>C (n.862-3T>C) c.753-3T>C c.1012-3T>C (n.1012-3T>C) n.514-3T>C n.625T>C c.820-3T>C (n.820-3T>C) c.637-3T>C (n.637-3T>C) | gnomAD v4 |
1 | g.77933280A>C | CA340876465 | NEXN | c.1054-2A>C (n.1054-2A>C) c.862-2A>C (n.862-2A>C) c.753-2A>C c.1012-2A>C (n.1012-2A>C) n.514-2A>C n.626A>C c.820-2A>C (n.820-2A>C) c.637-2A>C (n.637-2A>C) | |
1 | g.77933280A>G | CA340876468 | NEXN | c.1054-2A>G (n.1054-2A>G) c.862-2A>G (n.862-2A>G) c.753-2A>G c.1012-2A>G (n.1012-2A>G) n.514-2A>G n.626A>G c.820-2A>G (n.820-2A>G) c.637-2A>G (n.637-2A>G) | |
1 | g.77933280A>T | CA340876470 | NEXN | c.1054-2A>T (n.1054-2A>T) c.862-2A>T (n.862-2A>T) c.753-2A>T c.1012-2A>T (n.1012-2A>T) n.514-2A>T n.626A>T c.820-2A>T (n.820-2A>T) c.637-2A>T (n.637-2A>T) | |
1 | g.77933281G>A | CA340876472 | NEXN | c.1054-1G>A (n.1054-1G>A) c.862-1G>A (n.862-1G>A) c.753-1G>A c.1012-1G>A (n.1012-1G>A) n.514-1G>A n.627G>A c.820-1G>A (n.820-1G>A) c.637-1G>A (n.637-1G>A) | gnomAD v4 |
1 | g.77933281G>C | CA340876473 | NEXN | c.1054-1G>C (n.1054-1G>C) c.862-1G>C (n.862-1G>C) c.753-1G>C c.1012-1G>C (n.1012-1G>C) n.514-1G>C n.627G>C c.820-1G>C (n.820-1G>C) c.637-1G>C (n.637-1G>C) | |
1 | g.77933281G>T | CA340876475 | NEXN | c.1054-1G>T (n.1054-1G>T) c.862-1G>T (n.862-1G>T) c.753-1G>T c.1012-1G>T (n.1012-1G>T) n.514-1G>T n.627G>T c.820-1G>T (n.820-1G>T) c.637-1G>T (n.637-1G>T) | |
1 | g.77933282G>A | CA340876476 | NEXN | c.1054G>A (p.Val352Ile) c.862G>A (p.Val288Ile) c.753G>A c.1012G>A (p.Val338Ile) n.514G>A n.628G>A c.820G>A (p.Val274Ile) c.637G>A (p.Val213Ile) | gnomAD v4 |
1 | g.77933282G>C | CA340876478 | NEXN | c.1054G>C (p.Val352Leu) c.862G>C (p.Val288Leu) c.753G>C c.1012G>C (p.Val338Leu) n.514G>C n.628G>C c.820G>C (p.Val274Leu) c.637G>C (p.Val213Leu) | |
1 | g.77933282G>T | CA340876479 | NEXN | c.1054G>T (p.Val352Leu) c.862G>T (p.Val288Leu) c.753G>T c.1012G>T (p.Val338Leu) n.514G>T n.628G>T c.820G>T (p.Val274Leu) c.637G>T (p.Val213Leu) | |
1 | g.77933283T>A | CA340876483 | NEXN | c.1055T>A (p.Val352Glu) c.863T>A (p.Val288Glu) c.754T>A c.1013T>A (p.Val338Glu) n.515T>A n.629T>A c.821T>A (p.Val274Glu) c.638T>A (p.Val213Glu) | gnomAD v4 |
1 | g.77933283T>C | CA24684063 | NEXN | c.1055T>C (p.Val352Ala) c.863T>C (p.Val288Ala) c.754T>C c.1013T>C (p.Val338Ala) n.515T>C n.629T>C c.821T>C (p.Val274Ala) c.638T>C (p.Val213Ala) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.77933283T>G | CA340876481 | NEXN | c.1055T>G (p.Val352Gly) c.863T>G (p.Val288Gly) c.754T>G c.1013T>G (p.Val338Gly) n.515T>G n.629T>G c.821T>G (p.Val274Gly) c.638T>G (p.Val213Gly) | |
1 | g.77933283T= | CA1177626656 | NEXN | c.1055T= (p.Val352=) c.863T= (p.Val288=) c.754T= c.1013T= (p.Val338=) n.515T= n.629T= c.821T= (p.Val274=) c.638T= (p.Val213=) | |
1 | g.77933284A>C | CA418572031 | NEXN | c.1056A>C (p.Val352=) c.864A>C (p.Val288=) c.755A>C c.1014A>C (p.Val338=) n.516A>C n.630A>C c.822A>C (p.Val274=) c.639A>C (p.Val213=) | |
1 | g.77933284A>G | CA418572032 | NEXN | c.1056A>G (p.Val352=) c.864A>G (p.Val288=) c.755A>G c.1014A>G (p.Val338=) n.516A>G n.630A>G c.822A>G (p.Val274=) c.639A>G (p.Val213=) | gnomAD v4 |
1 | g.77933284A>T | CA418572033 | NEXN | c.1056A>T (p.Val352=) c.864A>T (p.Val288=) c.755A>T c.1014A>T (p.Val338=) n.516A>T n.630A>T c.822A>T (p.Val274=) c.639A>T (p.Val213=) | |
1 | g.77933285G>A | CA24684065 | NEXN | c.1057G>A (p.Val353Ile) c.865G>A (p.Val289Ile) c.756G>A c.1015G>A (p.Val339Ile) n.517G>A n.631G>A c.823G>A (p.Val275Ile) c.640G>A (p.Val214Ile) | ClinVar dbSNP |
1 | g.77933285G>C | CA340876487 | NEXN | c.1057G>C (p.Val353Leu) c.865G>C (p.Val289Leu) c.756G>C c.1015G>C (p.Val339Leu) n.517G>C n.631G>C c.823G>C (p.Val275Leu) c.640G>C (p.Val214Leu) | |
1 | g.77933285G= | CA1177626659 | NEXN | c.1057G= (p.Val353=) c.865G= (p.Val289=) c.756G= c.1015G= (p.Val339=) n.517G= n.631G= c.823G= (p.Val275=) c.640G= (p.Val214=) | |
1 | g.77933285G>T | CA340876489 | NEXN | c.1057G>T (p.Val353Leu) c.865G>T (p.Val289Leu) c.756G>T c.1015G>T (p.Val339Leu) n.517G>T n.631G>T c.823G>T (p.Val275Leu) c.640G>T (p.Val214Leu) | |
1 | g.77933286T>A | CA340876491 | NEXN | c.1058T>A (p.Val353Glu) c.866T>A (p.Val289Glu) c.757T>A c.1016T>A (p.Val339Glu) n.518T>A n.632T>A c.824T>A (p.Val275Glu) c.641T>A (p.Val214Glu) | |
1 | g.77933286T>C | CA340876493 | NEXN | c.1058T>C (p.Val353Ala) c.866T>C (p.Val289Ala) c.757T>C c.1016T>C (p.Val339Ala) n.518T>C n.632T>C c.824T>C (p.Val275Ala) c.641T>C (p.Val214Ala) | gnomAD v4 |
1 | g.77933286T>G | CA340876495 | NEXN | c.1058T>G (p.Val353Gly) c.866T>G (p.Val289Gly) c.757T>G c.1016T>G (p.Val339Gly) n.518T>G n.632T>G c.824T>G (p.Val275Gly) c.641T>G (p.Val214Gly) | |
1 | g.77933286_77933292delinsTAGATGA | CA1177626662 | NEXN | c.1058_1064delinsTAGATGA (p.Val353=) c.866_872delinsTAGATGA (p.Val289=) c.757_763delinsTAGATGA c.1016_1022delinsTAGATGA (p.Val339=) n.518_524delinsTAGATGA n.632_638delinsTAGATGA c.824_830delinsTAGATGA (p.Val275=) c.641_647delinsTAGATGA (p.Val214=) | |
1 | g.77933287A>C | CA418572034 | NEXN | c.1059A>C (p.Val353=) c.867A>C (p.Val289=) c.758A>C c.1017A>C (p.Val339=) n.519A>C n.633A>C c.825A>C (p.Val275=) c.642A>C (p.Val214=) | |
1 | g.77933287A>G | CA418572035 | NEXN | c.1059A>G (p.Val353=) c.867A>G (p.Val289=) c.758A>G c.1017A>G (p.Val339=) n.519A>G n.633A>G c.825A>G (p.Val275=) c.642A>G (p.Val214=) | |
1 | g.77933287A>T | CA418572036 | NEXN | c.1059A>T (p.Val353=) c.867A>T (p.Val289=) c.758A>T c.1017A>T (p.Val339=) n.519A>T n.633A>T c.825A>T (p.Val275=) c.642A>T (p.Val214=) | |
1 | g.77933287_77933292del | CA524231365 | NEXN | c.1059_1064del (p.Asp354_Asp355del) c.867_872del (p.Asp290_Asp291del) c.758_763del c.1017_1022del (p.Asp340_Asp341del) n.519_524del n.633_638del c.825_830del (p.Asp276_Asp277del) c.642_647del (p.Asp215_Asp216del) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.77933288G>A | CA340876499 | NEXN | c.1060G>A (p.Asp354Asn) c.868G>A (p.Asp290Asn) c.759G>A c.1018G>A (p.Asp340Asn) n.520G>A n.634G>A c.826G>A (p.Asp276Asn) c.643G>A (p.Asp215Asn) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.77933288G>C | CA340876500 | NEXN | c.1060G>C (p.Asp354His) c.868G>C (p.Asp290His) c.759G>C c.1018G>C (p.Asp340His) n.520G>C n.634G>C c.826G>C (p.Asp276His) c.643G>C (p.Asp215His) | dbSNP |
1 | g.77933288G= | CA1177626664 | NEXN | c.1060G= (p.Asp354=) c.868G= (p.Asp290=) c.759G= c.1018G= (p.Asp340=) n.520G= n.634G= c.826G= (p.Asp276=) c.643G= (p.Asp215=) | |
1 | g.77933288G>T | CA340876502 | NEXN | c.1060G>T (p.Asp354Tyr) c.868G>T (p.Asp290Tyr) c.759G>T c.1018G>T (p.Asp340Tyr) n.520G>T n.634G>T c.826G>T (p.Asp276Tyr) c.643G>T (p.Asp215Tyr) | |
1 | g.77933289A>C | CA340876504 | NEXN | c.1061A>C (p.Asp354Ala) c.869A>C (p.Asp290Ala) c.760A>C c.1019A>C (p.Asp340Ala) n.521A>C n.635A>C c.827A>C (p.Asp276Ala) c.644A>C (p.Asp215Ala) | |
1 | g.77933289A>G | CA340876507 | NEXN | c.1061A>G (p.Asp354Gly) c.869A>G (p.Asp290Gly) c.760A>G c.1019A>G (p.Asp340Gly) n.521A>G n.635A>G c.827A>G (p.Asp276Gly) c.644A>G (p.Asp215Gly) | |
1 | g.77933289A>T | CA340876508 | NEXN | c.1061A>T (p.Asp354Val) c.869A>T (p.Asp290Val) c.760A>T c.1019A>T (p.Asp340Val) n.521A>T n.635A>T c.827A>T (p.Asp276Val) c.644A>T (p.Asp215Val) | |
1 | g.77933290T>A | CA340876514 | NEXN | c.1062T>A (p.Asp354Glu) c.870T>A (p.Asp290Glu) c.761T>A c.1020T>A (p.Asp340Glu) n.522T>A n.636T>A c.828T>A (p.Asp276Glu) c.645T>A (p.Asp215Glu) | |
1 | g.77933290T>C | CA418572037 | NEXN | c.1062T>C (p.Asp354=) c.870T>C (p.Asp290=) c.761T>C c.1020T>C (p.Asp340=) n.522T>C n.636T>C c.828T>C (p.Asp276=) c.645T>C (p.Asp215=) | |
1 | g.77933290T>G | CA340876516 | NEXN | c.1062T>G (p.Asp354Glu) c.870T>G (p.Asp290Glu) c.761T>G c.1020T>G (p.Asp340Glu) n.522T>G n.636T>G c.828T>G (p.Asp276Glu) c.645T>G (p.Asp215Glu) | |
1 | g.77933291G>A | CA340876519 | NEXN | c.1063G>A (p.Asp355Asn) c.871G>A (p.Asp291Asn) c.762G>A c.1021G>A (p.Asp341Asn) n.523G>A n.637G>A c.829G>A (p.Asp277Asn) c.646G>A (p.Asp216Asn) | |
1 | g.77933291G>C | CA340876521 | NEXN | c.1063G>C (p.Asp355His) c.871G>C (p.Asp291His) c.762G>C c.1021G>C (p.Asp341His) n.523G>C n.637G>C c.829G>C (p.Asp277His) c.646G>C (p.Asp216His) | ClinVar dbSNP gnomAD v4 |
1 | g.77933291G= | CA1177626666 | NEXN | c.1063G= (p.Asp355=) c.871G= (p.Asp291=) c.762G= c.1021G= (p.Asp341=) n.523G= n.637G= c.829G= (p.Asp277=) c.646G= (p.Asp216=) | |
1 | g.77933291G>T | CA340876518 | NEXN | c.1063G>T (p.Asp355Tyr) c.871G>T (p.Asp291Tyr) c.762G>T c.1021G>T (p.Asp341Tyr) n.523G>T n.637G>T c.829G>T (p.Asp277Tyr) c.646G>T (p.Asp216Tyr) | gnomAD v4 |
1 | g.77933291_77933299dup | CA2646274518 | NEXN | c.1063_1071dup (p.Ser357_Pro358insAspAspSer) c.871_879dup (p.Ser293_Pro294insAspAspSer) c.762_770dup c.1021_1029dup (p.Ser343_Pro344insAspAspSer) n.523_531dup n.637_645dup c.829_837dup (p.Ser279_Pro280insAspAspSer) c.646_654dup (p.Ser218_Pro219insAspAspSer) | gnomAD v4 |
1 | g.77933292A= | CA1177626669 | NEXN | c.1064A= (p.Asp355=) c.872A= (p.Asp291=) c.763A= c.1022A= (p.Asp341=) n.524A= n.638A= c.830A= (p.Asp277=) c.647A= (p.Asp216=) | |
1 | g.77933292A>C | CA340876523 | NEXN | c.1064A>C (p.Asp355Ala) c.872A>C (p.Asp291Ala) c.763A>C c.1022A>C (p.Asp341Ala) n.524A>C n.638A>C c.830A>C (p.Asp277Ala) c.647A>C (p.Asp216Ala) | dbSNP |
1 | g.77933292A>G | CA340876525 | NEXN | c.1064A>G (p.Asp355Gly) c.872A>G (p.Asp291Gly) c.763A>G c.1022A>G (p.Asp341Gly) n.524A>G n.638A>G c.830A>G (p.Asp277Gly) c.647A>G (p.Asp216Gly) | ClinVar |
1 | g.77933292A>T | CA340876528 | NEXN | c.1064A>T (p.Asp355Val) c.872A>T (p.Asp291Val) c.763A>T c.1022A>T (p.Asp341Val) n.524A>T n.638A>T c.830A>T (p.Asp277Val) c.647A>T (p.Asp216Val) | |
1 | g.77933293T>A | CA340876531 | NEXN | c.1065T>A (p.Asp355Glu) c.873T>A (p.Asp291Glu) c.764T>A c.1023T>A (p.Asp341Glu) n.525T>A n.639T>A c.831T>A (p.Asp277Glu) c.648T>A (p.Asp216Glu) | |
1 | g.77933293T>C | CA177488 | NEXN | c.1065T>C (p.Asp355=) c.873T>C (p.Asp291=) c.764T>C c.1023T>C (p.Asp341=) n.525T>C n.639T>C c.831T>C (p.Asp277=) c.648T>C (p.Asp216=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933293T>G | CA340876535 | NEXN | c.1065T>G (p.Asp355Glu) c.873T>G (p.Asp291Glu) c.764T>G c.1023T>G (p.Asp341Glu) n.525T>G n.639T>G c.831T>G (p.Asp277Glu) c.648T>G (p.Asp216Glu) | |
1 | g.77933293T= | CA1143694066 | NEXN | c.1065T= (p.Asp355=) c.873T= (p.Asp291=) c.764T= c.1023T= (p.Asp341=) n.525T= n.639T= c.831T= (p.Asp277=) c.648T= (p.Asp216=) | |
1 | g.77933294G>A | CA340876537 | NEXN | c.1066G>A (p.Asp356Asn) c.874G>A (p.Asp292Asn) c.765G>A c.1024G>A (p.Asp342Asn) n.526G>A n.640G>A c.832G>A (p.Asp278Asn) c.649G>A (p.Asp217Asn) | COSMIC COSMIC |
1 | g.77933294G>C | CA340876539 | NEXN | c.1066G>C (p.Asp356His) c.874G>C (p.Asp292His) c.765G>C c.1024G>C (p.Asp342His) n.526G>C n.640G>C c.832G>C (p.Asp278His) c.649G>C (p.Asp217His) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933294G= | CA1177626673 | NEXN | c.1066G= (p.Asp356=) c.874G= (p.Asp292=) c.765G= c.1024G= (p.Asp342=) n.526G= n.640G= c.832G= (p.Asp278=) c.649G= (p.Asp217=) | |
1 | g.77933294G>T | CA340876541 | NEXN | c.1066G>T (p.Asp356Tyr) c.874G>T (p.Asp292Tyr) c.765G>T c.1024G>T (p.Asp342Tyr) n.526G>T n.640G>T c.832G>T (p.Asp278Tyr) c.649G>T (p.Asp217Tyr) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.77933295A>C | CA340876544 | NEXN | c.1067A>C (p.Asp356Ala) c.875A>C (p.Asp292Ala) c.766A>C c.1025A>C (p.Asp342Ala) n.527A>C n.641A>C c.833A>C (p.Asp278Ala) c.650A>C (p.Asp217Ala) | |
1 | g.77933295A>G | CA340876546 | NEXN | c.1067A>G (p.Asp356Gly) c.875A>G (p.Asp292Gly) c.766A>G c.1025A>G (p.Asp342Gly) n.527A>G n.641A>G c.833A>G (p.Asp278Gly) c.650A>G (p.Asp217Gly) | |
1 | g.77933295A>T | CA340876548 | NEXN | c.1067A>T (p.Asp356Val) c.875A>T (p.Asp292Val) c.766A>T c.1025A>T (p.Asp342Val) n.527A>T n.641A>T c.833A>T (p.Asp278Val) c.650A>T (p.Asp217Val) | |
1 | g.77933296C>A | CA340876551 | NEXN | c.1068C>A (p.Asp356Glu) c.876C>A (p.Asp292Glu) c.767C>A c.1026C>A (p.Asp342Glu) n.528C>A n.642C>A c.834C>A (p.Asp278Glu) c.651C>A (p.Asp217Glu) | gnomAD v4 |
1 | g.77933296C= | CA1177626675 | NEXN | c.1068C= (p.Asp356=) c.876C= (p.Asp292=) c.767C= c.1026C= (p.Asp342=) n.528C= n.642C= c.834C= (p.Asp278=) c.651C= (p.Asp217=) | |
1 | g.77933296C>G | CA340876549 | NEXN | c.1068C>G (p.Asp356Glu) c.876C>G (p.Asp292Glu) c.767C>G c.1026C>G (p.Asp342Glu) n.528C>G n.642C>G c.834C>G (p.Asp278Glu) c.651C>G (p.Asp217Glu) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.77933296C>T | CA418572038 | NEXN | c.1068C>T (p.Asp356=) c.876C>T (p.Asp292=) c.767C>T c.1026C>T (p.Asp342=) n.528C>T n.642C>T c.834C>T (p.Asp278=) c.651C>T (p.Asp217=) | |
1 | g.77933297T>A | CA340876553 | NEXN | c.1069T>A (p.Ser357Thr) c.877T>A (p.Ser293Thr) c.768T>A c.1027T>A (p.Ser343Thr) n.529T>A n.643T>A c.835T>A (p.Ser279Thr) c.652T>A (p.Ser218Thr) | |
1 | g.77933297T>C | CA340876557 | NEXN | c.1069T>C (p.Ser357Pro) c.877T>C (p.Ser293Pro) c.768T>C c.1027T>C (p.Ser343Pro) n.529T>C n.643T>C c.835T>C (p.Ser279Pro) c.652T>C (p.Ser218Pro) | COSMIC COSMIC |
1 | g.77933297T>G | CA340876558 | NEXN | c.1069T>G (p.Ser357Ala) c.877T>G (p.Ser293Ala) c.768T>G c.1027T>G (p.Ser343Ala) n.529T>G n.643T>G c.835T>G (p.Ser279Ala) c.652T>G (p.Ser218Ala) | |
1 | g.77933298C>A | CA340876561 | NEXN | c.1070C>A (p.Ser357Tyr) c.878C>A (p.Ser293Tyr) c.769C>A c.1028C>A (p.Ser343Tyr) n.530C>A n.644C>A c.836C>A (p.Ser279Tyr) c.653C>A (p.Ser218Tyr) | gnomAD v4 |
1 | g.77933298C= | CA1177626676 | NEXN | c.1070C= (p.Ser357=) c.878C= (p.Ser293=) c.769C= c.1028C= (p.Ser343=) n.530C= n.644C= c.836C= (p.Ser279=) c.653C= (p.Ser218=) | |
1 | g.77933298C>G | CA340876563 | NEXN | c.1070C>G (p.Ser357Cys) c.878C>G (p.Ser293Cys) c.769C>G c.1028C>G (p.Ser343Cys) n.530C>G n.644C>G c.836C>G (p.Ser279Cys) c.653C>G (p.Ser218Cys) | |
1 | g.77933298C>T | CA918800 | NEXN | c.1070C>T (p.Ser357Phe) c.878C>T (p.Ser293Phe) c.769C>T c.1028C>T (p.Ser343Phe) n.530C>T n.644C>T c.836C>T (p.Ser279Phe) c.653C>T (p.Ser218Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.77933299C>A | CA418572039 | NEXN | c.1071C>A (p.Ser357=) c.879C>A (p.Ser293=) c.770C>A c.1029C>A (p.Ser343=) n.531C>A n.645C>A c.837C>A (p.Ser279=) c.654C>A (p.Ser218=) | |
1 | g.77933299C= | CA1177626678 | NEXN | c.1071C= (p.Ser357=) c.879C= (p.Ser293=) c.770C= c.1029C= (p.Ser343=) n.531C= n.645C= c.837C= (p.Ser279=) c.654C= (p.Ser218=) | |
1 | g.77933299C>G | CA418572040 | NEXN | c.1071C>G (p.Ser357=) c.879C>G (p.Ser293=) c.770C>G c.1029C>G (p.Ser343=) n.531C>G n.645C>G c.837C>G (p.Ser279=) c.654C>G (p.Ser218=) | |
1 | g.77933299C>T | CA418572041 | NEXN | c.1071C>T (p.Ser357=) c.879C>T (p.Ser293=) c.770C>T c.1029C>T (p.Ser343=) n.531C>T n.645C>T c.837C>T (p.Ser279=) c.654C>T (p.Ser218=) | |
1 | g.77933299_77933300insTTT | CA24684091 | NEXN | c.1071_1072insTTT (p.Ser357_Pro358insPhe) c.879_880insTTT (p.Ser293_Pro294insPhe) c.770_771insTTT c.1029_1030insTTT (p.Ser343_Pro344insPhe) n.531_532insTTT n.645_646insTTT c.837_838insTTT (p.Ser279_Pro280insPhe) c.654_655insTTT (p.Ser218_Pro219insPhe) | dbSNP |
1 | g.77933300C>A | CA340876565 | NEXN | c.1072C>A (p.Pro358Thr) c.880C>A (p.Pro294Thr) c.771C>A c.1030C>A (p.Pro344Thr) n.532C>A n.646C>A c.838C>A (p.Pro280Thr) c.655C>A (p.Pro219Thr) | |
1 | g.77933300C= | CA1177626680 | NEXN | c.1072C= (p.Pro358=) c.880C= (p.Pro294=) c.771C= c.1030C= (p.Pro344=) n.532C= n.646C= c.838C= (p.Pro280=) c.655C= (p.Pro219=) | |
1 | g.77933300C>G | CA340876566 | NEXN | c.1072C>G (p.Pro358Ala) c.880C>G (p.Pro294Ala) c.771C>G c.1030C>G (p.Pro344Ala) n.532C>G n.646C>G c.838C>G (p.Pro280Ala) c.655C>G (p.Pro219Ala) | |
1 | g.77933300C>T | CA24684103 | NEXN | c.1072C>T (p.Pro358Ser) c.880C>T (p.Pro294Ser) c.771C>T c.1030C>T (p.Pro344Ser) n.532C>T n.646C>T c.838C>T (p.Pro280Ser) c.655C>T (p.Pro219Ser) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.77933301C>A | CA340876569 | NEXN | c.1073C>A (p.Pro358Gln) c.881C>A (p.Pro294Gln) c.772C>A c.1031C>A (p.Pro344Gln) n.533C>A n.647C>A c.839C>A (p.Pro280Gln) c.656C>A (p.Pro219Gln) | |
1 | g.77933301C= | CA1177626682 | NEXN | c.1073C= (p.Pro358=) c.881C= (p.Pro294=) c.772C= c.1031C= (p.Pro344=) n.533C= n.647C= c.839C= (p.Pro280=) c.656C= (p.Pro219=) | |
1 | g.77933301C>G | CA340876571 | NEXN | c.1073C>G (p.Pro358Arg) c.881C>G (p.Pro294Arg) c.772C>G c.1031C>G (p.Pro344Arg) n.533C>G n.647C>G c.839C>G (p.Pro280Arg) c.656C>G (p.Pro219Arg) | |
1 | g.77933301C>T | CA918801 | NEXN | c.1073C>T (p.Pro358Leu) c.881C>T (p.Pro294Leu) c.772C>T c.1031C>T (p.Pro344Leu) n.533C>T n.647C>T c.839C>T (p.Pro280Leu) c.656C>T (p.Pro219Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.77933302A>C | CA418572042 | NEXN | c.1074A>C (p.Pro358=) c.882A>C (p.Pro294=) c.773A>C c.1032A>C (p.Pro344=) n.534A>C n.648A>C c.840A>C (p.Pro280=) c.657A>C (p.Pro219=) | |
1 | g.77933302A>G | CA418572043 | NEXN | c.1074A>G (p.Pro358=) c.882A>G (p.Pro294=) c.773A>G c.1032A>G (p.Pro344=) n.534A>G n.648A>G c.840A>G (p.Pro280=) c.657A>G (p.Pro219=) | |
1 | g.77933302A>T | CA418572044 | NEXN | c.1074A>T (p.Pro358=) c.882A>T (p.Pro294=) c.773A>T c.1032A>T (p.Pro344=) n.534A>T n.648A>T c.840A>T (p.Pro280=) c.657A>T (p.Pro219=) | |
1 | g.77933303G>A | CA340876579 | NEXN | c.1075G>A (p.Glu359Lys) c.883G>A (p.Glu295Lys) c.774G>A c.1033G>A (p.Glu345Lys) n.535G>A n.649G>A c.841G>A (p.Glu281Lys) c.658G>A (p.Glu220Lys) | |
1 | g.77933303G>C | CA340876581 | NEXN | c.1075G>C (p.Glu359Gln) c.883G>C (p.Glu295Gln) c.774G>C c.1033G>C (p.Glu345Gln) n.535G>C n.649G>C c.841G>C (p.Glu281Gln) c.658G>C (p.Glu220Gln) | |
1 | g.77933303G>T | CA340876577 | NEXN | c.1075G>T (p.Glu359Ter) c.883G>T (p.Glu295Ter) c.774G>T c.1033G>T (p.Glu345Ter) n.535G>T n.649G>T c.841G>T (p.Glu281Ter) c.658G>T (p.Glu220Ter) | |
1 | g.77933304A>C | CA340876583 | NEXN | c.1076A>C (p.Glu359Ala) c.884A>C (p.Glu295Ala) c.775A>C c.1034A>C (p.Glu345Ala) n.536A>C n.650A>C c.842A>C (p.Glu281Ala) c.659A>C (p.Glu220Ala) | |
1 | g.77933304A>G | CA340876582 | NEXN | c.1076A>G (p.Glu359Gly) c.884A>G (p.Glu295Gly) c.775A>G c.1034A>G (p.Glu345Gly) n.536A>G n.650A>G c.842A>G (p.Glu281Gly) c.659A>G (p.Glu220Gly) | |
1 | g.77933304A>T | CA340876585 | NEXN | c.1076A>T (p.Glu359Val) c.884A>T (p.Glu295Val) c.775A>T c.1034A>T (p.Glu345Val) n.536A>T n.650A>T c.842A>T (p.Glu281Val) c.659A>T (p.Glu220Val) | |
1 | g.77933305G>A | CA418572045 | NEXN | c.1077G>A (p.Glu359=) c.885G>A (p.Glu295=) c.776G>A c.1035G>A (p.Glu345=) n.537G>A n.651G>A c.843G>A (p.Glu281=) c.660G>A (p.Glu220=) | |
1 | g.77933305G>C | CA340876587 | NEXN | c.1077G>C (p.Glu359Asp) c.885G>C (p.Glu295Asp) c.776G>C c.1035G>C (p.Glu345Asp) n.537G>C n.651G>C c.843G>C (p.Glu281Asp) c.660G>C (p.Glu220Asp) | |
1 | g.77933305G= | CA1177626683 | NEXN | c.1077G= (p.Glu359=) c.885G= (p.Glu295=) c.776G= c.1035G= (p.Glu345=) n.537G= n.651G= c.843G= (p.Glu281=) c.660G= (p.Glu220=) | |
1 | g.77933305G>T | CA340876589 | NEXN | c.1077G>T (p.Glu359Asp) c.885G>T (p.Glu295Asp) c.776G>T c.1035G>T (p.Glu345Asp) n.537G>T n.651G>T c.843G>T (p.Glu281Asp) c.660G>T (p.Glu220Asp) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.77933306A>C | CA340876590 | NEXN | c.1078A>C (p.Met360Leu) c.886A>C (p.Met296Leu) c.777A>C c.1036A>C (p.Met346Leu) n.538A>C n.652A>C c.844A>C (p.Met282Leu) c.661A>C (p.Met221Leu) | |
1 | g.77933306A>G | CA340876591 | NEXN | c.1078A>G (p.Met360Val) c.886A>G (p.Met296Val) c.777A>G c.1036A>G (p.Met346Val) n.538A>G n.652A>G c.844A>G (p.Met282Val) c.661A>G (p.Met221Val) | ClinVar gnomAD v4 |
1 | g.77933306A>T | CA340876593 | NEXN | c.1078A>T (p.Met360Leu) c.886A>T (p.Met296Leu) c.777A>T c.1036A>T (p.Met346Leu) n.538A>T n.652A>T c.844A>T (p.Met282Leu) c.661A>T (p.Met221Leu) | gnomAD v4 |
1 | g.77933307T>A | CA340876594 | NEXN | c.1079T>A (p.Met360Lys) c.887T>A (p.Met296Lys) c.778T>A c.1037T>A (p.Met346Lys) n.539T>A n.653T>A c.845T>A (p.Met282Lys) c.662T>A (p.Met221Lys) | |
1 | g.77933307T>C | CA340876596 | NEXN | c.1079T>C (p.Met360Thr) c.887T>C (p.Met296Thr) c.778T>C c.1037T>C (p.Met346Thr) n.539T>C n.653T>C c.845T>C (p.Met282Thr) c.662T>C (p.Met221Thr) | gnomAD v4 |
1 | g.77933307T>G | CA340876598 | NEXN | c.1079T>G (p.Met360Arg) c.887T>G (p.Met296Arg) c.778T>G c.1037T>G (p.Met346Arg) n.539T>G n.653T>G c.845T>G (p.Met282Arg) c.662T>G (p.Met221Arg) | |
1 | g.77933308G>A | CA340876599 | NEXN | c.1080G>A (p.Met360Ile) c.888G>A (p.Met296Ile) c.779G>A c.1038G>A (p.Met346Ile) n.540G>A n.654G>A c.846G>A (p.Met282Ile) c.663G>A (p.Met221Ile) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.77933308G>C | CA340876600 | NEXN | c.1080G>C (p.Met360Ile) c.888G>C (p.Met296Ile) c.779G>C c.1038G>C (p.Met346Ile) n.540G>C n.654G>C c.846G>C (p.Met282Ile) c.663G>C (p.Met221Ile) | |
1 | g.77933308G= | CA1177626685 | NEXN | c.1080G= (p.Met360=) c.888G= (p.Met296=) c.779G= c.1038G= (p.Met346=) n.540G= n.654G= c.846G= (p.Met282=) c.663G= (p.Met221=) | |
1 | g.77933308G>T | CA340876601 | NEXN | c.1080G>T (p.Met360Ile) c.888G>T (p.Met296Ile) c.779G>T c.1038G>T (p.Met346Ile) n.540G>T n.654G>T c.846G>T (p.Met282Ile) c.663G>T (p.Met221Ile) | |
1 | g.77933309T>A | CA340876602 | NEXN | c.1081T>A (p.Tyr361Asn) c.889T>A (p.Tyr297Asn) c.780T>A c.1039T>A (p.Tyr347Asn) n.541T>A n.655T>A c.847T>A (p.Tyr283Asn) c.664T>A (p.Tyr222Asn) | |
1 | g.77933309T>C | CA340876603 | NEXN | c.1081T>C (p.Tyr361His) c.889T>C (p.Tyr297His) c.780T>C c.1039T>C (p.Tyr347His) n.541T>C n.655T>C c.847T>C (p.Tyr283His) c.664T>C (p.Tyr222His) | |
1 | g.77933309T>G | CA340876604 | NEXN | c.1081T>G (p.Tyr361Asp) c.889T>G (p.Tyr297Asp) c.780T>G c.1039T>G (p.Tyr347Asp) n.541T>G n.655T>G c.847T>G (p.Tyr283Asp) c.664T>G (p.Tyr222Asp) | |
1 | g.77933310A= | CA1145347785 | NEXN | c.1082A= (p.Tyr361=) c.890A= (p.Tyr297=) c.781A= c.1040A= (p.Tyr347=) n.542A= n.656A= c.848A= (p.Tyr283=) c.665A= (p.Tyr222=) | |
1 | g.77933310A>C | CA340876605 | NEXN | c.1082A>C (p.Tyr361Ser) c.890A>C (p.Tyr297Ser) c.781A>C c.1040A>C (p.Tyr347Ser) n.542A>C n.656A>C c.848A>C (p.Tyr283Ser) c.665A>C (p.Tyr222Ser) | |
1 | g.77933310A>G | CA24684109 | NEXN | c.1082A>G (p.Tyr361Cys) c.890A>G (p.Tyr297Cys) c.781A>G c.1040A>G (p.Tyr347Cys) n.542A>G n.656A>G c.848A>G (p.Tyr283Cys) c.665A>G (p.Tyr222Cys) | dbSNP gnomAD v4 |
1 | g.77933310A>T | CA340876606 | NEXN | c.1082A>T (p.Tyr361Phe) c.890A>T (p.Tyr297Phe) c.781A>T c.1040A>T (p.Tyr347Phe) n.542A>T n.656A>T c.848A>T (p.Tyr283Phe) c.665A>T (p.Tyr222Phe) | |
1 | g.77933311T>A | CA340876608 | NEXN | c.1083T>A (p.Tyr361Ter) c.891T>A (p.Tyr297Ter) c.782T>A c.1041T>A (p.Tyr347Ter) n.543T>A n.657T>A c.849T>A (p.Tyr283Ter) c.666T>A (p.Tyr222Ter) | |
1 | g.77933311T>C | CA16610154 | NEXN | c.1083T>C (p.Tyr361=) c.891T>C (p.Tyr297=) c.782T>C c.1041T>C (p.Tyr347=) n.543T>C n.657T>C c.849T>C (p.Tyr283=) c.666T>C (p.Tyr222=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
1 | g.77933311T>G | CA340876611 | NEXN | c.1083T>G (p.Tyr361Ter) c.891T>G (p.Tyr297Ter) c.782T>G c.1041T>G (p.Tyr347Ter) n.543T>G n.657T>G c.849T>G (p.Tyr283Ter) c.666T>G (p.Tyr222Ter) | |
1 | g.77933311T= | CA1177626687 | NEXN | c.1083T= (p.Tyr361=) c.891T= (p.Tyr297=) c.782T= c.1041T= (p.Tyr347=) n.543T= n.657T= c.849T= (p.Tyr283=) c.666T= (p.Tyr222=) | |
1 | g.77933312A= | CA1177626688 | NEXN | c.1084A= (p.Lys362=) c.892A= (p.Lys298=) c.783A= c.1042A= (p.Lys348=) n.544A= n.658A= c.850A= (p.Lys284=) c.667A= (p.Lys223=) | |
1 | g.77933312A>C | CA918802 | NEXN | c.1084A>C (p.Lys362Gln) c.892A>C (p.Lys298Gln) c.783A>C c.1042A>C (p.Lys348Gln) n.544A>C n.658A>C c.850A>C (p.Lys284Gln) c.667A>C (p.Lys223Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933312A>G | CA340876613 | NEXN | c.1084A>G (p.Lys362Glu) c.892A>G (p.Lys298Glu) c.783A>G c.1042A>G (p.Lys348Glu) n.544A>G n.658A>G c.850A>G (p.Lys284Glu) c.667A>G (p.Lys223Glu) | |
1 | g.77933312A>T | CA340876615 | NEXN | c.1084A>T (p.Lys362Ter) c.892A>T (p.Lys298Ter) c.783A>T c.1042A>T (p.Lys348Ter) n.544A>T n.658A>T c.850A>T (p.Lys284Ter) c.667A>T (p.Lys223Ter) | ClinVar |
1 | g.77933313del | CA2574414088 | NEXN | c.1085del (p.Lys362ArgfsTer21) c.893del (p.Lys298ArgfsTer21) c.784del c.1043del (p.Lys348ArgfsTer21) n.545del n.659del c.851del (p.Lys284ArgfsTer21) c.668del (p.Lys223ArgfsTer21) | |
1 | g.77933313A>C | CA340876625 | NEXN | c.1085A>C (p.Lys362Thr) c.893A>C (p.Lys298Thr) c.784A>C c.1043A>C (p.Lys348Thr) n.545A>C n.659A>C c.851A>C (p.Lys284Thr) c.668A>C (p.Lys223Thr) | |
1 | g.77933313A>G | CA340876626 | NEXN | c.1085A>G (p.Lys362Arg) c.893A>G (p.Lys298Arg) c.784A>G c.1043A>G (p.Lys348Arg) n.545A>G n.659A>G c.851A>G (p.Lys284Arg) c.668A>G (p.Lys223Arg) | |
1 | g.77933313A>T | CA340876628 | NEXN | c.1085A>T (p.Lys362Met) c.893A>T (p.Lys298Met) c.784A>T c.1043A>T (p.Lys348Met) n.545A>T n.659A>T c.851A>T (p.Lys284Met) c.668A>T (p.Lys223Met) | |
1 | g.77933314G>A | CA418572046 | NEXN | c.1086G>A (p.Lys362=) c.894G>A (p.Lys298=) c.785G>A c.1044G>A (p.Lys348=) n.546G>A n.660G>A c.852G>A (p.Lys284=) c.669G>A (p.Lys223=) | |
1 | g.77933314G>C | CA340876631 | NEXN | c.1086G>C (p.Lys362Asn) c.894G>C (p.Lys298Asn) c.785G>C c.1044G>C (p.Lys348Asn) n.546G>C n.660G>C c.852G>C (p.Lys284Asn) c.669G>C (p.Lys223Asn) | |
1 | g.77933314G>T | CA340876632 | NEXN | c.1086G>T (p.Lys362Asn) c.894G>T (p.Lys298Asn) c.785G>T c.1044G>T (p.Lys348Asn) n.546G>T n.660G>T c.852G>T (p.Lys284Asn) c.669G>T (p.Lys223Asn) | gnomAD v4 |
1 | g.77933315A>C | CA340876636 | NEXN | c.1087A>C (p.Thr363Pro) c.895A>C (p.Thr299Pro) c.786A>C c.1045A>C (p.Thr349Pro) n.547A>C n.661A>C c.853A>C (p.Thr285Pro) c.670A>C (p.Thr224Pro) | |
1 | g.77933315A>G | CA340876638 | NEXN | c.1087A>G (p.Thr363Ala) c.895A>G (p.Thr299Ala) c.786A>G c.1045A>G (p.Thr349Ala) n.547A>G n.661A>G c.853A>G (p.Thr285Ala) c.670A>G (p.Thr224Ala) | |
1 | g.77933315A>T | CA340876634 | NEXN | c.1087A>T (p.Thr363Ser) c.895A>T (p.Thr299Ser) c.786A>T c.1045A>T (p.Thr349Ser) n.547A>T n.661A>T c.853A>T (p.Thr285Ser) c.670A>T (p.Thr224Ser) | |
1 | g.77933316C>A | CA340876639 | NEXN | c.1088C>A (p.Thr363Lys) c.896C>A (p.Thr299Lys) c.787C>A c.1046C>A (p.Thr349Lys) n.548C>A n.662C>A c.854C>A (p.Thr285Lys) c.671C>A (p.Thr224Lys) | |
1 | g.77933316C= | CA1148876825 | NEXN | c.1088C= (p.Thr363=) c.896C= (p.Thr299=) c.787C= c.1046C= (p.Thr349=) n.548C= n.662C= c.854C= (p.Thr285=) c.671C= (p.Thr224=) | |
1 | g.77933316C>G | CA918803 | NEXN | c.1088C>G (p.Thr363Arg) c.896C>G (p.Thr299Arg) c.787C>G c.1046C>G (p.Thr349Arg) n.548C>G n.662C>G c.854C>G (p.Thr285Arg) c.671C>G (p.Thr224Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933316C>T | CA340876642 | NEXN | c.1088C>T (p.Thr363Ile) c.896C>T (p.Thr299Ile) c.787C>T c.1046C>T (p.Thr349Ile) n.548C>T n.662C>T c.854C>T (p.Thr285Ile) c.671C>T (p.Thr224Ile) | ClinVar dbSNP |
1 | g.77933317A= | CA1177626692 | NEXN | c.1089A= (p.Thr363=) c.897A= (p.Thr299=) c.788A= c.1047A= (p.Thr349=) n.549A= n.663A= c.855A= (p.Thr285=) c.672A= (p.Thr224=) | |
1 | g.77933317A>C | CA10581817 | NEXN | c.1089A>C (p.Thr363=) c.897A>C (p.Thr299=) c.788A>C c.1047A>C (p.Thr349=) n.549A>C n.663A>C c.855A>C (p.Thr285=) c.672A>C (p.Thr224=) | ClinVar dbSNP gnomAD v4 |
1 | g.77933317A>G | CA418572048 | NEXN | c.1089A>G (p.Thr363=) c.897A>G (p.Thr299=) c.788A>G c.1047A>G (p.Thr349=) n.549A>G n.663A>G c.855A>G (p.Thr285=) c.672A>G (p.Thr224=) | |
1 | g.77933317A>T | CA418572047 | NEXN | c.1089A>T (p.Thr363=) c.897A>T (p.Thr299=) c.788A>T c.1047A>T (p.Thr349=) n.549A>T n.663A>T c.855A>T (p.Thr285=) c.672A>T (p.Thr224=) | |
1 | g.77933318A>C | CA340876646 | NEXN | c.1090A>C (p.Ile364Leu) c.898A>C (p.Ile300Leu) c.789A>C c.1048A>C (p.Ile350Leu) n.550A>C n.664A>C c.856A>C (p.Ile286Leu) c.673A>C (p.Ile225Leu) | |
1 | g.77933318A>G | CA340876648 | NEXN | c.1090A>G (p.Ile364Val) c.898A>G (p.Ile300Val) c.789A>G c.1048A>G (p.Ile350Val) n.550A>G n.664A>G c.856A>G (p.Ile286Val) c.673A>G (p.Ile225Val) | gnomAD v4 |
1 | g.77933318A>T | CA340876652 | NEXN | c.1090A>T (p.Ile364Phe) c.898A>T (p.Ile300Phe) c.789A>T c.1048A>T (p.Ile350Phe) n.550A>T n.664A>T c.856A>T (p.Ile286Phe) c.673A>T (p.Ile225Phe) | |
1 | g.77933319T>A | CA340876655 | NEXN | c.1091T>A (p.Ile364Asn) c.899T>A (p.Ile300Asn) c.790T>A c.1049T>A (p.Ile350Asn) n.551T>A n.665T>A c.857T>A (p.Ile286Asn) c.674T>A (p.Ile225Asn) | gnomAD v4 |
1 | g.77933319T>C | CA340876659 | NEXN | c.1091T>C (p.Ile364Thr) c.899T>C (p.Ile300Thr) c.790T>C c.1049T>C (p.Ile350Thr) n.551T>C n.665T>C c.857T>C (p.Ile286Thr) c.674T>C (p.Ile225Thr) | gnomAD v4 |
1 | g.77933319T>G | CA340876657 | NEXN | c.1091T>G (p.Ile364Ser) c.899T>G (p.Ile300Ser) c.790T>G c.1049T>G (p.Ile350Ser) n.551T>G n.665T>G c.857T>G (p.Ile286Ser) c.674T>G (p.Ile225Ser) | |
1 | g.77933320C>A | CA418572049 | NEXN | c.1092C>A (p.Ile364=) c.900C>A (p.Ile300=) c.791C>A c.1050C>A (p.Ile350=) n.552C>A n.666C>A c.858C>A (p.Ile286=) c.675C>A (p.Ile225=) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.77933320C= | CA1177626696 | NEXN | c.1092C= (p.Ile364=) c.900C= (p.Ile300=) c.791C= c.1050C= (p.Ile350=) n.552C= n.666C= c.858C= (p.Ile286=) c.675C= (p.Ile225=) | |
1 | g.77933320C>G | CA340876660 | NEXN | c.1092C>G (p.Ile364Met) c.900C>G (p.Ile300Met) c.791C>G c.1050C>G (p.Ile350Met) n.552C>G n.666C>G c.858C>G (p.Ile286Met) c.675C>G (p.Ile225Met) | |
1 | g.77933320C>T | CA418572050 | NEXN | c.1092C>T (p.Ile364=) c.900C>T (p.Ile300=) c.791C>T c.1050C>T (p.Ile350=) n.552C>T n.666C>T c.858C>T (p.Ile286=) c.675C>T (p.Ile225=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933321T>A | CA340876661 | NEXN | c.1093T>A (p.Ser365Thr) c.901T>A (p.Ser301Thr) c.792T>A c.1051T>A (p.Ser351Thr) n.553T>A n.667T>A c.859T>A (p.Ser287Thr) c.676T>A (p.Ser226Thr) | |
1 | g.77933321T>C | CA340876662 | NEXN | c.1093T>C (p.Ser365Pro) c.901T>C (p.Ser301Pro) c.792T>C c.1051T>C (p.Ser351Pro) n.553T>C n.667T>C c.859T>C (p.Ser287Pro) c.676T>C (p.Ser226Pro) | |
1 | g.77933321T>G | CA340876663 | NEXN | c.1093T>G (p.Ser365Ala) c.901T>G (p.Ser301Ala) c.792T>G c.1051T>G (p.Ser351Ala) n.553T>G n.667T>G c.859T>G (p.Ser287Ala) c.676T>G (p.Ser226Ala) | |
1 | g.77933322C>A | CA340876664 | NEXN | c.1094C>A (p.Ser365Tyr) c.902C>A (p.Ser301Tyr) c.793C>A c.1052C>A (p.Ser351Tyr) n.554C>A n.668C>A c.860C>A (p.Ser287Tyr) c.677C>A (p.Ser226Tyr) | |
1 | g.77933322C= | CA1177626698 | NEXN | c.1094C= (p.Ser365=) c.902C= (p.Ser301=) c.793C= c.1052C= (p.Ser351=) n.554C= n.668C= c.860C= (p.Ser287=) c.677C= (p.Ser226=) | |
1 | g.77933322C>G | CA335406 | NEXN | c.1094C>G (p.Ser365Cys) c.902C>G (p.Ser301Cys) c.793C>G c.1052C>G (p.Ser351Cys) n.554C>G n.668C>G c.860C>G (p.Ser287Cys) c.677C>G (p.Ser226Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.77933322C>T | CA340876665 | NEXN | c.1094C>T (p.Ser365Phe) c.902C>T (p.Ser301Phe) c.793C>T c.1052C>T (p.Ser351Phe) n.554C>T n.668C>T c.860C>T (p.Ser287Phe) c.677C>T (p.Ser226Phe) | |
1 | g.77933323T>A | CA418572051 | NEXN | c.1095T>A (p.Ser365=) c.903T>A (p.Ser301=) c.794T>A c.1053T>A (p.Ser351=) n.555T>A n.669T>A c.861T>A (p.Ser287=) c.678T>A (p.Ser226=) | |
1 | g.77933323T>C | CA418572052 | NEXN | c.1095T>C (p.Ser365=) c.903T>C (p.Ser301=) c.794T>C c.1053T>C (p.Ser351=) n.555T>C n.669T>C c.861T>C (p.Ser287=) c.678T>C (p.Ser226=) | |
1 | g.77933323T>G | CA418572053 | NEXN | c.1095T>G (p.Ser365=) c.903T>G (p.Ser301=) c.794T>G c.1053T>G (p.Ser351=) n.555T>G n.669T>G c.861T>G (p.Ser287=) c.678T>G (p.Ser226=) | |
1 | g.77933324C>A | CA340876666 | NEXN | c.1096C>A (p.Gln366Lys) c.904C>A (p.Gln302Lys) c.795C>A c.1054C>A (p.Gln352Lys) n.556C>A n.670C>A c.862C>A (p.Gln288Lys) c.679C>A (p.Gln227Lys) | |
1 | g.77933324C>G | CA340876668 | NEXN | c.1096C>G (p.Gln366Glu) c.904C>G (p.Gln302Glu) c.795C>G c.1054C>G (p.Gln352Glu) n.556C>G n.670C>G c.862C>G (p.Gln288Glu) c.679C>G (p.Gln227Glu) | |
1 | g.77933324C>T | CA340876670 | NEXN | c.1096C>T (p.Gln366Ter) c.904C>T (p.Gln302Ter) c.795C>T c.1054C>T (p.Gln352Ter) n.556C>T n.670C>T c.862C>T (p.Gln288Ter) c.679C>T (p.Gln227Ter) | gnomAD v4 |
1 | g.77933325A>C | CA340876671 | NEXN | c.1097A>C (p.Gln366Pro) c.905A>C (p.Gln302Pro) c.796A>C c.1055A>C (p.Gln352Pro) n.557A>C n.671A>C c.863A>C (p.Gln288Pro) c.680A>C (p.Gln227Pro) | gnomAD v4 |
1 | g.77933325A>G | CA340876673 | NEXN | c.1097A>G (p.Gln366Arg) c.905A>G (p.Gln302Arg) c.796A>G c.1055A>G (p.Gln352Arg) n.557A>G n.671A>G c.863A>G (p.Gln288Arg) c.680A>G (p.Gln227Arg) | |
1 | g.77933325A>T | CA340876675 | NEXN | c.1097A>T (p.Gln366Leu) c.905A>T (p.Gln302Leu) c.796A>T c.1055A>T (p.Gln352Leu) n.557A>T n.671A>T c.863A>T (p.Gln288Leu) c.680A>T (p.Gln227Leu) | |
1 | g.77933326A>C | CA340876676 | NEXN | c.1098A>C (p.Gln366His) c.906A>C (p.Gln302His) c.797A>C c.1056A>C (p.Gln352His) n.558A>C n.672A>C c.864A>C (p.Gln288His) c.681A>C (p.Gln227His) | |
1 | g.77933326A>G | CA418572054 | NEXN | c.1098A>G (p.Gln366=) c.906A>G (p.Gln302=) c.797A>G c.1056A>G (p.Gln352=) n.558A>G n.672A>G c.864A>G (p.Gln288=) c.681A>G (p.Gln227=) | |
1 | g.77933326A>T | CA340876678 | NEXN | c.1098A>T (p.Gln366His) c.906A>T (p.Gln302His) c.797A>T c.1056A>T (p.Gln352His) n.558A>T n.672A>T c.864A>T (p.Gln288His) c.681A>T (p.Gln227His) | gnomAD v4 |
1 | g.77933327G>A | CA918804 | NEXN | c.1099G>A (p.Glu367Lys) c.907G>A (p.Glu303Lys) c.798G>A c.1057G>A (p.Glu353Lys) n.559G>A n.673G>A c.865G>A (p.Glu289Lys) c.682G>A (p.Glu228Lys) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
1 | g.77933327G>C | CA340876679 | NEXN | c.1099G>C (p.Glu367Gln) c.907G>C (p.Glu303Gln) c.798G>C c.1057G>C (p.Glu353Gln) n.559G>C n.673G>C c.865G>C (p.Glu289Gln) c.682G>C (p.Glu228Gln) | |
1 | g.77933327G= | CA1177626700 | NEXN | c.1099G= (p.Glu367=) c.907G= (p.Glu303=) c.798G= c.1057G= (p.Glu353=) n.559G= n.673G= c.865G= (p.Glu289=) c.682G= (p.Glu228=) | |
1 | g.77933327G>T | CA340876682 | NEXN | c.1099G>T (p.Glu367Ter) c.907G>T (p.Glu303Ter) c.798G>T c.1057G>T (p.Glu353Ter) n.559G>T n.673G>T c.865G>T (p.Glu289Ter) c.682G>T (p.Glu228Ter) | |
1 | g.77933328A= | CA1177626702 | NEXN | c.1100A= (p.Glu367=) c.908A= (p.Glu303=) c.799A= c.1058A= (p.Glu353=) n.560A= n.674A= c.866A= (p.Glu289=) c.683A= (p.Glu228=) | |
1 | g.77933328A>C | CA340876688 | NEXN | c.1100A>C (p.Glu367Ala) c.908A>C (p.Glu303Ala) c.799A>C c.1058A>C (p.Glu353Ala) n.560A>C n.674A>C c.866A>C (p.Glu289Ala) c.683A>C (p.Glu228Ala) | |
1 | g.77933328A>G | CA340876686 | NEXN | c.1100A>G (p.Glu367Gly) c.908A>G (p.Glu303Gly) c.799A>G c.1058A>G (p.Glu353Gly) n.560A>G n.674A>G c.866A>G (p.Glu289Gly) c.683A>G (p.Glu228Gly) | dbSNP gnomAD v4 |
1 | g.77933328A>T | CA340876684 | NEXN | c.1100A>T (p.Glu367Val) c.908A>T (p.Glu303Val) c.799A>T c.1058A>T (p.Glu353Val) n.560A>T n.674A>T c.866A>T (p.Glu289Val) c.683A>T (p.Glu228Val) | |
1 | g.77933329A>C | CA340876689 | NEXN | c.1101A>C (p.Glu367Asp) c.909A>C (p.Glu303Asp) c.800A>C c.1059A>C (p.Glu353Asp) n.561A>C n.675A>C c.867A>C (p.Glu289Asp) c.684A>C (p.Glu228Asp) | |
1 | g.77933329A>G | CA418572055 | NEXN | c.1101A>G (p.Glu367=) c.909A>G (p.Glu303=) c.800A>G c.1059A>G (p.Glu353=) n.561A>G n.675A>G c.867A>G (p.Glu289=) c.684A>G (p.Glu228=) | |
1 | g.77933329A>T | CA340876691 | NEXN | c.1101A>T (p.Glu367Asp) c.909A>T (p.Glu303Asp) c.800A>T c.1059A>T (p.Glu353Asp) n.561A>T n.675A>T c.867A>T (p.Glu289Asp) c.684A>T (p.Glu228Asp) | |
1 | g.77933330T>A | CA340876694 | NEXN | c.1102T>A (p.Phe368Ile) c.910T>A (p.Phe304Ile) c.801T>A c.1060T>A (p.Phe354Ile) n.562T>A n.676T>A c.868T>A (p.Phe290Ile) c.685T>A (p.Phe229Ile) | |
1 | g.77933330T>C | CA340876695 | NEXN | c.1102T>C (p.Phe368Leu) c.910T>C (p.Phe304Leu) c.801T>C c.1060T>C (p.Phe354Leu) n.562T>C n.676T>C c.868T>C (p.Phe290Leu) c.685T>C (p.Phe229Leu) | gnomAD v4 |
1 | g.77933330T>G | CA340876697 | NEXN | c.1102T>G (p.Phe368Val) c.910T>G (p.Phe304Val) c.801T>G c.1060T>G (p.Phe354Val) n.562T>G n.676T>G c.868T>G (p.Phe290Val) c.685T>G (p.Phe229Val) | |
1 | g.77933331T>A | CA340876700 | NEXN | c.1103T>A (p.Phe368Tyr) c.911T>A (p.Phe304Tyr) c.802T>A c.1061T>A (p.Phe354Tyr) n.563T>A n.677T>A c.869T>A (p.Phe290Tyr) c.686T>A (p.Phe229Tyr) | |
1 | g.77933331T>C | CA340876701 | NEXN | c.1103T>C (p.Phe368Ser) c.911T>C (p.Phe304Ser) c.802T>C c.1061T>C (p.Phe354Ser) n.563T>C n.677T>C c.869T>C (p.Phe290Ser) c.686T>C (p.Phe229Ser) | |
1 | g.77933331T>G | CA340876702 | NEXN | c.1103T>G (p.Phe368Cys) c.911T>G (p.Phe304Cys) c.802T>G c.1061T>G (p.Phe354Cys) n.563T>G n.677T>G c.869T>G (p.Phe290Cys) c.686T>G (p.Phe229Cys) | |
1 | g.77933332T>A | CA340876703 | NEXN | c.1104T>A (p.Phe368Leu) c.912T>A (p.Phe304Leu) c.803T>A c.1062T>A (p.Phe354Leu) n.564T>A n.678T>A c.870T>A (p.Phe290Leu) c.687T>A (p.Phe229Leu) | |
1 | g.77933332T>C | CA418572056 | NEXN | c.1104T>C (p.Phe368=) c.912T>C (p.Phe304=) c.803T>C c.1062T>C (p.Phe354=) n.564T>C n.678T>C c.870T>C (p.Phe290=) c.687T>C (p.Phe229=) | |
1 | g.77933332T>G | CA340876704 | NEXN | c.1104T>G (p.Phe368Leu) c.912T>G (p.Phe304Leu) c.803T>G c.1062T>G (p.Phe354Leu) n.564T>G n.678T>G c.870T>G (p.Phe290Leu) c.687T>G (p.Phe229Leu) | |
1 | g.77933333C>A | CA340876705 | NEXN | c.1105C>A (p.Leu369Ile) c.913C>A (p.Leu305Ile) c.804C>A c.1063C>A (p.Leu355Ile) n.565C>A n.679C>A c.871C>A (p.Leu291Ile) c.688C>A (p.Leu230Ile) | |
1 | g.77933333C>G | CA340876706 | NEXN | c.1105C>G (p.Leu369Val) c.913C>G (p.Leu305Val) c.804C>G c.1063C>G (p.Leu355Val) n.565C>G n.679C>G c.871C>G (p.Leu291Val) c.688C>G (p.Leu230Val) | |
1 | g.77933333C>T | CA340876707 | NEXN | c.1105C>T (p.Leu369Phe) c.913C>T (p.Leu305Phe) c.804C>T c.1063C>T (p.Leu355Phe) n.565C>T n.679C>T c.871C>T (p.Leu291Phe) c.688C>T (p.Leu230Phe) | |
1 | g.77933334T>A | CA340876710 | NEXN | c.1106T>A (p.Leu369His) c.914T>A (p.Leu305His) c.805T>A c.1064T>A (p.Leu355His) n.566T>A n.680T>A c.872T>A (p.Leu291His) c.689T>A (p.Leu230His) | |
1 | g.77933334T>C | CA340876709 | NEXN | c.1106T>C (p.Leu369Pro) c.914T>C (p.Leu305Pro) c.805T>C c.1064T>C (p.Leu355Pro) n.566T>C n.680T>C c.872T>C (p.Leu291Pro) c.689T>C (p.Leu230Pro) | |
1 | g.77933334T>G | CA340876708 | NEXN | c.1106T>G (p.Leu369Arg) c.914T>G (p.Leu305Arg) c.805T>G c.1064T>G (p.Leu355Arg) n.566T>G n.680T>G c.872T>G (p.Leu291Arg) c.689T>G (p.Leu230Arg) | |
1 | g.77933335T>A | CA418572057 | NEXN | c.1107T>A (p.Leu369=) c.915T>A (p.Leu305=) c.806T>A c.1065T>A (p.Leu355=) n.567T>A n.681T>A c.873T>A (p.Leu291=) c.690T>A (p.Leu230=) | |
1 | g.77933335T>C | CA418572058 | NEXN | c.1107T>C (p.Leu369=) c.915T>C (p.Leu305=) c.806T>C c.1065T>C (p.Leu355=) n.567T>C n.681T>C c.873T>C (p.Leu291=) c.690T>C (p.Leu230=) | |
1 | g.77933335T>G | CA418572059 | NEXN | c.1107T>G (p.Leu369=) c.915T>G (p.Leu305=) c.806T>G c.1065T>G (p.Leu355=) n.567T>G n.681T>G c.873T>G (p.Leu291=) c.690T>G (p.Leu230=) | |
1 | g.77933336A= | CA1177626703 | NEXN | c.1108A= (p.Thr370=) c.916A= (p.Thr306=) c.807A= c.1066A= (p.Thr356=) n.568A= n.682A= c.874A= (p.Thr292=) c.691A= (p.Thr231=) | |
1 | g.77933336A>C | CA340876711 | NEXN | c.1108A>C (p.Thr370Pro) c.916A>C (p.Thr306Pro) c.807A>C c.1066A>C (p.Thr356Pro) n.568A>C n.682A>C c.874A>C (p.Thr292Pro) c.691A>C (p.Thr231Pro) | |
1 | g.77933336A>G | CA340876712 | NEXN | c.1108A>G (p.Thr370Ala) c.916A>G (p.Thr306Ala) c.807A>G c.1066A>G (p.Thr356Ala) n.568A>G n.682A>G c.874A>G (p.Thr292Ala) c.691A>G (p.Thr231Ala) | ClinVar dbSNP |
1 | g.77933336A>T | CA340876713 | NEXN | c.1108A>T (p.Thr370Ser) c.916A>T (p.Thr306Ser) c.807A>T c.1066A>T (p.Thr356Ser) n.568A>T n.682A>T c.874A>T (p.Thr292Ser) c.691A>T (p.Thr231Ser) | |
1 | g.77933337C>A | CA340876714 | NEXN | c.1109C>A (p.Thr370Lys) c.917C>A (p.Thr306Lys) c.808C>A c.1067C>A (p.Thr356Lys) n.569C>A n.683C>A c.875C>A (p.Thr292Lys) c.692C>A (p.Thr231Lys) | |
1 | g.77933337C>G | CA340876715 | NEXN | c.1109C>G (p.Thr370Arg) c.917C>G (p.Thr306Arg) c.808C>G c.1067C>G (p.Thr356Arg) n.569C>G n.683C>G c.875C>G (p.Thr292Arg) c.692C>G (p.Thr231Arg) | |
1 | g.77933337C>T | CA340876716 | NEXN | c.1109C>T (p.Thr370Ile) c.917C>T (p.Thr306Ile) c.808C>T c.1067C>T (p.Thr356Ile) n.569C>T n.683C>T c.875C>T (p.Thr292Ile) c.692C>T (p.Thr231Ile) | |
1 | g.77933338A= | CA1145570309 | NEXN | c.1110A= (p.Thr370=) c.918A= (p.Thr306=) c.809A= c.1068A= (p.Thr356=) n.570A= n.684A= c.876A= (p.Thr292=) c.693A= (p.Thr231=) | |
1 | g.77933338A>C | CA418572060 | NEXN | c.1110A>C (p.Thr370=) c.918A>C (p.Thr306=) c.809A>C c.1068A>C (p.Thr356=) n.570A>C n.684A>C c.876A>C (p.Thr292=) c.693A>C (p.Thr231=) | |
1 | g.77933338A>G | CA418572061 | NEXN | c.1110A>G (p.Thr370=) c.918A>G (p.Thr306=) c.809A>G c.1068A>G (p.Thr356=) n.570A>G n.684A>G c.876A>G (p.Thr292=) c.693A>G (p.Thr231=) | |
1 | g.77933338A>T | CA918805 | NEXN | c.1110A>T (p.Thr370=) c.918A>T (p.Thr306=) c.809A>T c.1068A>T (p.Thr356=) n.570A>T n.684A>T c.876A>T (p.Thr292=) c.693A>T (p.Thr231=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933339C>A | CA340876717 | NEXN | c.1111C>A (p.Pro371Thr) c.919C>A (p.Pro307Thr) c.810C>A c.1069C>A (p.Pro357Thr) n.571C>A n.685C>A c.877C>A (p.Pro293Thr) c.694C>A (p.Pro232Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933339C= | CA1177626706 | NEXN | c.1111C= (p.Pro371=) c.919C= (p.Pro307=) c.810C= c.1069C= (p.Pro357=) n.571C= n.685C= c.877C= (p.Pro293=) c.694C= (p.Pro232=) | |
1 | g.77933339C>G | CA340876718 | NEXN | c.1111C>G (p.Pro371Ala) c.919C>G (p.Pro307Ala) c.810C>G c.1069C>G (p.Pro357Ala) n.571C>G n.685C>G c.877C>G (p.Pro293Ala) c.694C>G (p.Pro232Ala) | |
1 | g.77933339C>T | CA340876719 | NEXN | c.1111C>T (p.Pro371Ser) c.919C>T (p.Pro307Ser) c.810C>T c.1069C>T (p.Pro357Ser) n.571C>T n.685C>T c.877C>T (p.Pro293Ser) c.694C>T (p.Pro232Ser) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.77933340C>A | CA24684201 | NEXN | c.1112C>A (p.Pro371Gln) c.920C>A (p.Pro307Gln) c.811C>A c.1070C>A (p.Pro357Gln) n.572C>A n.686C>A c.878C>A (p.Pro293Gln) c.695C>A (p.Pro232Gln) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933340C= | CA1143393216 | NEXN | c.1112C= (p.Pro371=) c.920C= (p.Pro307=) c.811C= c.1070C= (p.Pro357=) n.572C= n.686C= c.878C= (p.Pro293=) c.695C= (p.Pro232=) | |
1 | g.77933340C>G | CA340876720 | NEXN | c.1112C>G (p.Pro371Arg) c.920C>G (p.Pro307Arg) c.811C>G c.1070C>G (p.Pro357Arg) n.572C>G n.686C>G c.878C>G (p.Pro293Arg) c.695C>G (p.Pro232Arg) | |
1 | g.77933340C>T | CA142104 | NEXN | c.1112C>T (p.Pro371Leu) c.920C>T (p.Pro307Leu) c.811C>T c.1070C>T (p.Pro357Leu) n.572C>T n.686C>T c.878C>T (p.Pro293Leu) c.695C>T (p.Pro232Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933341G>A | CA918806 | NEXN | c.1113G>A (p.Pro371=) c.921G>A (p.Pro307=) c.812G>A c.1071G>A (p.Pro357=) n.573G>A n.687G>A c.879G>A (p.Pro293=) c.696G>A (p.Pro232=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
1 | g.77933341G>C | CA418572062 | NEXN | c.1113G>C (p.Pro371=) c.921G>C (p.Pro307=) c.812G>C c.1071G>C (p.Pro357=) n.573G>C n.687G>C c.879G>C (p.Pro293=) c.696G>C (p.Pro232=) | |
1 | g.77933341G= | CA1177626711 | NEXN | c.1113G= (p.Pro371=) c.921G= (p.Pro307=) c.812G= c.1071G= (p.Pro357=) n.573G= n.687G= c.879G= (p.Pro293=) c.696G= (p.Pro232=) | |
1 | g.77933341G>T | CA418572063 | NEXN | c.1113G>T (p.Pro371=) c.921G>T (p.Pro307=) c.812G>T c.1071G>T (p.Pro357=) n.573G>T n.687G>T c.879G>T (p.Pro293=) c.696G>T (p.Pro232=) | gnomAD v4 |
1 | g.77933342G>A | CA340876722 | NEXN | c.1114G>A (p.Gly372Arg) c.922G>A (p.Gly308Arg) c.813G>A c.1072G>A (p.Gly358Arg) n.574G>A n.688G>A c.880G>A (p.Gly294Arg) c.697G>A (p.Gly233Arg) | gnomAD v4 COSMIC COSMIC |
1 | g.77933342G>C | CA340876723 | NEXN | c.1114G>C (p.Gly372Arg) c.922G>C (p.Gly308Arg) c.813G>C c.1072G>C (p.Gly358Arg) n.574G>C n.688G>C c.880G>C (p.Gly294Arg) c.697G>C (p.Gly233Arg) | gnomAD v4 |
1 | g.77933342G>T | CA340876721 | NEXN | c.1114G>T (p.Gly372Ter) c.922G>T (p.Gly308Ter) c.813G>T c.1072G>T (p.Gly358Ter) n.574G>T n.688G>T c.880G>T (p.Gly294Ter) c.697G>T (p.Gly233Ter) | |
1 | g.77933343G>A | CA340876724 | NEXN | c.1115G>A (p.Gly372Glu) c.923G>A (p.Gly308Glu) c.814G>A c.1073G>A (p.Gly358Glu) n.575G>A n.689G>A c.881G>A (p.Gly294Glu) c.698G>A (p.Gly233Glu) | |
1 | g.77933343G>C | CA340876725 | NEXN | c.1115G>C (p.Gly372Ala) c.923G>C (p.Gly308Ala) c.814G>C c.1073G>C (p.Gly358Ala) n.575G>C n.689G>C c.881G>C (p.Gly294Ala) c.698G>C (p.Gly233Ala) | |
1 | g.77933343G>T | CA340876726 | NEXN | c.1115G>T (p.Gly372Val) c.923G>T (p.Gly308Val) c.814G>T c.1073G>T (p.Gly358Val) n.575G>T n.689G>T c.881G>T (p.Gly294Val) c.698G>T (p.Gly233Val) | gnomAD v4 |
1 | g.77933344A= | CA1177626713 | NEXN | c.1116A= (p.Gly372=) c.924A= (p.Gly308=) c.815A= c.1074A= (p.Gly358=) n.576A= n.690A= c.882A= (p.Gly294=) c.699A= (p.Gly233=) | |
1 | g.77933344A>C | CA418572064 | NEXN | c.1116A>C (p.Gly372=) c.924A>C (p.Gly308=) c.815A>C c.1074A>C (p.Gly358=) n.576A>C n.690A>C c.882A>C (p.Gly294=) c.699A>C (p.Gly233=) | |
1 | g.77933344A>G | CA418572065 | NEXN | c.1116A>G (p.Gly372=) c.924A>G (p.Gly308=) c.815A>G c.1074A>G (p.Gly358=) n.576A>G n.690A>G c.882A>G (p.Gly294=) c.699A>G (p.Gly233=) | dbSNP gnomAD v4 |
1 | g.77933344A>T | CA418572066 | NEXN | c.1116A>T (p.Gly372=) c.924A>T (p.Gly308=) c.815A>T c.1074A>T (p.Gly358=) n.576A>T n.690A>T c.882A>T (p.Gly294=) c.699A>T (p.Gly233=) | |
1 | g.77933345A= | CA1177626716 | NEXN | c.1117A= (p.Lys373=) c.925A= (p.Lys309=) c.816A= c.1075A= (p.Lys359=) n.577A= n.691A= c.883A= (p.Lys295=) c.700A= (p.Lys234=) | |
1 | g.77933345A>C | CA918807 | NEXN | c.1117A>C (p.Lys373Gln) c.925A>C (p.Lys309Gln) c.816A>C c.1075A>C (p.Lys359Gln) n.577A>C n.691A>C c.883A>C (p.Lys295Gln) c.700A>C (p.Lys234Gln) | dbSNP ExAC gnomAD v3 gnomAD v4 |
1 | g.77933345A>G | CA340876727 | NEXN | c.1117A>G (p.Lys373Glu) c.925A>G (p.Lys309Glu) c.816A>G c.1075A>G (p.Lys359Glu) n.577A>G n.691A>G c.883A>G (p.Lys295Glu) c.700A>G (p.Lys234Glu) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.77933345A>T | CA340876728 | NEXN | c.1117A>T (p.Lys373Ter) c.925A>T (p.Lys309Ter) c.816A>T c.1075A>T (p.Lys359Ter) n.577A>T n.691A>T c.883A>T (p.Lys295Ter) c.700A>T (p.Lys234Ter) | |
1 | g.77933346A>C | CA340876729 | NEXN | c.1118A>C (p.Lys373Thr) c.926A>C (p.Lys309Thr) c.817A>C c.1076A>C (p.Lys359Thr) n.578A>C n.692A>C c.884A>C (p.Lys295Thr) c.701A>C (p.Lys234Thr) | |
1 | g.77933346A>G | CA340876730 | NEXN | c.1118A>G (p.Lys373Arg) c.926A>G (p.Lys309Arg) c.817A>G c.1076A>G (p.Lys359Arg) n.578A>G n.692A>G c.884A>G (p.Lys295Arg) c.701A>G (p.Lys234Arg) | |
1 | g.77933346A>T | CA340876731 | NEXN | c.1118A>T (p.Lys373Ile) c.926A>T (p.Lys309Ile) c.817A>T c.1076A>T (p.Lys359Ile) n.578A>T n.692A>T c.884A>T (p.Lys295Ile) c.701A>T (p.Lys234Ile) | |
1 | g.77933347A>C | CA340876732 | NEXN | c.1119A>C (p.Lys373Asn) c.927A>C (p.Lys309Asn) c.818A>C c.1077A>C (p.Lys359Asn) n.579A>C n.693A>C c.885A>C (p.Lys295Asn) c.702A>C (p.Lys234Asn) | |
1 | g.77933347A>G | CA418572067 | NEXN | c.1119A>G (p.Lys373=) c.927A>G (p.Lys309=) c.818A>G c.1077A>G (p.Lys359=) n.579A>G n.693A>G c.885A>G (p.Lys295=) c.702A>G (p.Lys234=) | |
1 | g.77933347A>T | CA340876733 | NEXN | c.1119A>T (p.Lys373Asn) c.927A>T (p.Lys309Asn) c.818A>T c.1077A>T (p.Lys359Asn) n.579A>T n.693A>T c.885A>T (p.Lys295Asn) c.702A>T (p.Lys234Asn) | |
1 | g.77933348C>A | CA340876734 | NEXN | c.1120C>A (p.Leu374Met) c.928C>A (p.Leu310Met) c.819C>A c.1078C>A (p.Leu360Met) n.580C>A n.694C>A c.886C>A (p.Leu296Met) c.703C>A (p.Leu235Met) | |
1 | g.77933348C>G | CA340876735 | NEXN | c.1120C>G (p.Leu374Val) c.928C>G (p.Leu310Val) c.819C>G c.1078C>G (p.Leu360Val) n.580C>G n.694C>G c.886C>G (p.Leu296Val) c.703C>G (p.Leu235Val) | |
1 | g.77933348C>T | CA418572068 | NEXN | c.1120C>T (p.Leu374=) c.928C>T (p.Leu310=) c.819C>T c.1078C>T (p.Leu360=) n.580C>T n.694C>T c.886C>T (p.Leu296=) c.703C>T (p.Leu235=) | |
1 | g.77933349T>A | CA340876736 | NEXN | c.1121T>A (p.Leu374Gln) c.929T>A (p.Leu310Gln) c.820T>A c.1079T>A (p.Leu360Gln) n.581T>A n.695T>A c.887T>A (p.Leu296Gln) c.704T>A (p.Leu235Gln) | |
1 | g.77933349T>C | CA340876738 | NEXN | c.1121T>C (p.Leu374Pro) c.929T>C (p.Leu310Pro) c.820T>C c.1079T>C (p.Leu360Pro) n.581T>C n.695T>C c.887T>C (p.Leu296Pro) c.704T>C (p.Leu235Pro) | |
1 | g.77933349T>G | CA340876737 | NEXN | c.1121T>G (p.Leu374Arg) c.929T>G (p.Leu310Arg) c.820T>G c.1079T>G (p.Leu360Arg) n.581T>G n.695T>G c.887T>G (p.Leu296Arg) c.704T>G (p.Leu235Arg) | ClinVar gnomAD v4 |
1 | g.77933350G>A | CA418572069 | NEXN | c.1122G>A (p.Leu374=) c.930G>A (p.Leu310=) c.821G>A c.1080G>A (p.Leu360=) n.582G>A n.696G>A c.888G>A (p.Leu296=) c.705G>A (p.Leu235=) | |
1 | g.77933350G>C | CA418572070 | NEXN | c.1122G>C (p.Leu374=) c.930G>C (p.Leu310=) c.821G>C c.1080G>C (p.Leu360=) n.582G>C n.696G>C c.888G>C (p.Leu296=) c.705G>C (p.Leu235=) | |
1 | g.77933350G>T | CA418572071 | NEXN | c.1122G>T (p.Leu374=) c.930G>T (p.Leu310=) c.821G>T c.1080G>T (p.Leu360=) n.582G>T n.696G>T c.888G>T (p.Leu296=) c.705G>T (p.Leu235=) | |
1 | g.77933351G>A | CA340876739 | NEXN | c.1123G>A (p.Glu375Lys) c.931G>A (p.Glu311Lys) c.822G>A c.1081G>A (p.Glu361Lys) n.583G>A n.697G>A c.889G>A (p.Glu297Lys) c.706G>A (p.Glu236Lys) | |
1 | g.77933351G>C | CA340876740 | NEXN | c.1123G>C (p.Glu375Gln) c.931G>C (p.Glu311Gln) c.822G>C c.1081G>C (p.Glu361Gln) n.583G>C n.697G>C c.889G>C (p.Glu297Gln) c.706G>C (p.Glu236Gln) | |
1 | g.77933351G= | CA1177626720 | NEXN | c.1123G= (p.Glu375=) c.931G= (p.Glu311=) c.822G= c.1081G= (p.Glu361=) n.583G= n.697G= c.889G= (p.Glu297=) c.706G= (p.Glu236=) | |
1 | g.77933351G>T | CA340876741 | NEXN | c.1123G>T (p.Glu375Ter) c.931G>T (p.Glu311Ter) c.822G>T c.1081G>T (p.Glu361Ter) n.583G>T n.697G>T c.889G>T (p.Glu297Ter) c.706G>T (p.Glu236Ter) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
1 | g.77933352A>C | CA340876742 | NEXN | c.1124A>C (p.Glu375Ala) c.932A>C (p.Glu311Ala) c.823A>C c.1082A>C (p.Glu361Ala) n.584A>C n.698A>C c.890A>C (p.Glu297Ala) c.707A>C (p.Glu236Ala) | gnomAD v4 |
1 | g.77933352A>G | CA340876743 | NEXN | c.1124A>G (p.Glu375Gly) c.932A>G (p.Glu311Gly) c.823A>G c.1082A>G (p.Glu361Gly) n.584A>G n.698A>G c.890A>G (p.Glu297Gly) c.707A>G (p.Glu236Gly) | |
1 | g.77933352A>T | CA340876744 | NEXN | c.1124A>T (p.Glu375Val) c.932A>T (p.Glu311Val) c.823A>T c.1082A>T (p.Glu361Val) n.584A>T n.698A>T c.890A>T (p.Glu297Val) c.707A>T (p.Glu236Val) | |
1 | g.77933353A>C | CA340876746 | NEXN | c.1125A>C (p.Glu375Asp) c.933A>C (p.Glu311Asp) c.824A>C c.1083A>C (p.Glu361Asp) n.585A>C n.699A>C c.891A>C (p.Glu297Asp) c.708A>C (p.Glu236Asp) | |
1 | g.77933353A>G | CA418572072 | NEXN | c.1125A>G (p.Glu375=) c.933A>G (p.Glu311=) c.824A>G c.1083A>G (p.Glu361=) n.585A>G n.699A>G c.891A>G (p.Glu297=) c.708A>G (p.Glu236=) | |
1 | g.77933353A>T | CA340876747 | NEXN | c.1125A>T (p.Glu375Asp) c.933A>T (p.Glu311Asp) c.824A>T c.1083A>T (p.Glu361Asp) n.585A>T n.699A>T c.891A>T (p.Glu297Asp) c.708A>T (p.Glu236Asp) | |
1 | g.77933354A>C | CA340876748 | NEXN | c.1126A>C (p.Ile376Leu) c.934A>C (p.Ile312Leu) c.825A>C c.1084A>C (p.Ile362Leu) n.586A>C n.700A>C c.892A>C (p.Ile298Leu) c.709A>C (p.Ile237Leu) | |
1 | g.77933354A>G | CA340876750 | NEXN | c.1126A>G (p.Ile376Val) c.934A>G (p.Ile312Val) c.825A>G c.1084A>G (p.Ile362Val) n.586A>G n.700A>G c.892A>G (p.Ile298Val) c.709A>G (p.Ile237Val) | gnomAD v4 |
1 | g.77933354A>T | CA340876752 | NEXN | c.1126A>T (p.Ile376Phe) c.934A>T (p.Ile312Phe) c.825A>T c.1084A>T (p.Ile362Phe) n.586A>T n.700A>T c.892A>T (p.Ile298Phe) c.709A>T (p.Ile237Phe) | |
1 | g.77933355T>A | CA340876763 | NEXN | c.1127T>A (p.Ile376Asn) c.935T>A (p.Ile312Asn) c.826T>A c.1085T>A (p.Ile362Asn) n.587T>A n.701T>A c.893T>A (p.Ile298Asn) c.710T>A (p.Ile237Asn) | |
1 | g.77933355T>C | CA340876765 | NEXN | c.1127T>C (p.Ile376Thr) c.935T>C (p.Ile312Thr) c.826T>C c.1085T>C (p.Ile362Thr) n.587T>C n.701T>C c.893T>C (p.Ile298Thr) c.710T>C (p.Ile237Thr) | |
1 | g.77933355T>G | CA340876758 | NEXN | c.1127T>G (p.Ile376Ser) c.935T>G (p.Ile312Ser) c.826T>G c.1085T>G (p.Ile362Ser) n.587T>G n.701T>G c.893T>G (p.Ile298Ser) c.710T>G (p.Ile237Ser) | |
1 | g.77933356T>A | CA418572073 | NEXN | c.1128T>A (p.Ile376=) c.936T>A (p.Ile312=) c.827T>A c.1086T>A (p.Ile362=) n.588T>A n.702T>A c.894T>A (p.Ile298=) c.711T>A (p.Ile237=) | |
1 | g.77933356T>C | CA418572074 | NEXN | c.1128T>C (p.Ile376=) c.936T>C (p.Ile312=) c.827T>C c.1086T>C (p.Ile362=) n.588T>C n.702T>C c.894T>C (p.Ile298=) c.711T>C (p.Ile237=) | |
1 | g.77933356T>G | CA340876766 | NEXN | c.1128T>G (p.Ile376Met) c.936T>G (p.Ile312Met) c.827T>G c.1086T>G (p.Ile362Met) n.588T>G n.702T>G c.894T>G (p.Ile298Met) c.711T>G (p.Ile237Met) | |
1 | g.77933357A>C | CA340876768 | NEXN | c.1129A>C (p.Asn377His) c.937A>C (p.Asn313His) c.828A>C c.1087A>C (p.Asn363His) n.589A>C n.703A>C c.895A>C (p.Asn299His) c.712A>C (p.Asn238His) | |
1 | g.77933357A>G | CA340876773 | NEXN | c.1129A>G (p.Asn377Asp) c.937A>G (p.Asn313Asp) c.828A>G c.1087A>G (p.Asn363Asp) n.589A>G n.703A>G c.895A>G (p.Asn299Asp) c.712A>G (p.Asn238Asp) | |
1 | g.77933357A>T | CA340876770 | NEXN | c.1129A>T (p.Asn377Tyr) c.937A>T (p.Asn313Tyr) c.828A>T c.1087A>T (p.Asn363Tyr) n.589A>T n.703A>T c.895A>T (p.Asn299Tyr) c.712A>T (p.Asn238Tyr) | |
1 | g.77933358dup | CA2646274519 | NEXN | c.1130dup (p.Asn377LysfsTer3) c.938dup (p.Asn313LysfsTer3) c.829dup c.1088dup (p.Asn363LysfsTer3) n.590dup n.704dup c.896dup (p.Asn299LysfsTer3) c.713dup (p.Asn238LysfsTer3) | gnomAD v4 |
1 | g.77933358A>C | CA340876775 | NEXN | c.1130A>C (p.Asn377Thr) c.938A>C (p.Asn313Thr) c.829A>C c.1088A>C (p.Asn363Thr) n.590A>C n.704A>C c.896A>C (p.Asn299Thr) c.713A>C (p.Asn238Thr) | |
1 | g.77933358A>G | CA340876777 | NEXN | c.1130A>G (p.Asn377Ser) c.938A>G (p.Asn313Ser) c.829A>G c.1088A>G (p.Asn363Ser) n.590A>G n.704A>G c.896A>G (p.Asn299Ser) c.713A>G (p.Asn238Ser) | dbSNP gnomAD v4 |
1 | g.77933358A>T | CA340876779 | NEXN | c.1130A>T (p.Asn377Ile) c.938A>T (p.Asn313Ile) c.829A>T c.1088A>T (p.Asn363Ile) n.590A>T n.704A>T c.896A>T (p.Asn299Ile) c.713A>T (p.Asn238Ile) | |
1 | g.77933359T>A | CA340876789 | NEXN | c.1131T>A (p.Asn377Lys) c.939T>A (p.Asn313Lys) c.830T>A c.1089T>A (p.Asn363Lys) n.591T>A n.705T>A c.897T>A (p.Asn299Lys) c.714T>A (p.Asn238Lys) | COSMIC |
1 | g.77933359T>C | CA418572075 | NEXN | c.1131T>C (p.Asn377=) c.939T>C (p.Asn313=) c.830T>C c.1089T>C (p.Asn363=) n.591T>C n.705T>C c.897T>C (p.Asn299=) c.714T>C (p.Asn238=) | |
1 | g.77933359T>G | CA340876791 | NEXN | c.1131T>G (p.Asn377Lys) c.939T>G (p.Asn313Lys) c.830T>G c.1089T>G (p.Asn363Lys) n.591T>G n.705T>G c.897T>G (p.Asn299Lys) c.714T>G (p.Asn238Lys) | |
1 | g.77933360T>A | CA340876794 | NEXN | c.1132T>A (p.Phe378Ile) c.940T>A (p.Phe314Ile) c.831T>A c.1090T>A (p.Phe364Ile) n.592T>A n.706T>A c.898T>A (p.Phe300Ile) c.715T>A (p.Phe239Ile) | |
1 | g.77933360T>C | CA340876798 | NEXN | c.1132T>C (p.Phe378Leu) c.940T>C (p.Phe314Leu) c.831T>C c.1090T>C (p.Phe364Leu) n.592T>C n.706T>C c.898T>C (p.Phe300Leu) c.715T>C (p.Phe239Leu) | |
1 | g.77933360T>G | CA340876800 | NEXN | c.1132T>G (p.Phe378Val) c.940T>G (p.Phe314Val) c.831T>G c.1090T>G (p.Phe364Val) n.592T>G n.706T>G c.898T>G (p.Phe300Val) c.715T>G (p.Phe239Val) | |
1 | g.77933361T>A | CA340876803 | NEXN | c.1133T>A (p.Phe378Tyr) c.941T>A (p.Phe314Tyr) c.832T>A c.1091T>A (p.Phe364Tyr) n.593T>A n.707T>A c.899T>A (p.Phe300Tyr) c.716T>A (p.Phe239Tyr) | |
1 | g.77933361T>C | CA340876805 | NEXN | c.1133T>C (p.Phe378Ser) c.941T>C (p.Phe314Ser) c.832T>C c.1091T>C (p.Phe364Ser) n.593T>C n.707T>C c.899T>C (p.Phe300Ser) c.716T>C (p.Phe239Ser) | |
1 | g.77933361T>G | CA340876806 | NEXN | c.1133T>G (p.Phe378Cys) c.941T>G (p.Phe314Cys) c.832T>G c.1091T>G (p.Phe364Cys) n.593T>G n.707T>G c.899T>G (p.Phe300Cys) c.716T>G (p.Phe239Cys) | |
1 | g.77933362T>A | CA340876807 | NEXN | c.1134T>A (p.Phe378Leu) c.942T>A (p.Phe314Leu) c.833T>A c.1092T>A (p.Phe364Leu) n.594T>A n.708T>A c.900T>A (p.Phe300Leu) c.717T>A (p.Phe239Leu) | |
1 | g.77933362T>C | CA418572076 | NEXN | c.1134T>C (p.Phe378=) c.942T>C (p.Phe314=) c.833T>C c.1092T>C (p.Phe364=) n.594T>C n.708T>C c.900T>C (p.Phe300=) c.717T>C (p.Phe239=) | |
1 | g.77933362T>G | CA340876808 | NEXN | c.1134T>G (p.Phe378Leu) c.942T>G (p.Phe314Leu) c.833T>G c.1092T>G (p.Phe364Leu) n.594T>G n.708T>G c.900T>G (p.Phe300Leu) c.717T>G (p.Phe239Leu) | |
1 | g.77933363G>A | CA340876810 | NEXN | c.1135G>A (p.Glu379Lys) c.943G>A (p.Glu315Lys) c.834G>A c.1093G>A (p.Glu365Lys) n.595G>A n.709G>A c.901G>A (p.Glu301Lys) c.718G>A (p.Glu240Lys) | |
1 | g.77933363G>C | CA340876817 | NEXN | c.1135G>C (p.Glu379Gln) c.943G>C (p.Glu315Gln) c.834G>C c.1093G>C (p.Glu365Gln) n.595G>C n.709G>C c.901G>C (p.Glu301Gln) c.718G>C (p.Glu240Gln) | dbSNP |
1 | g.77933363G>T | CA340876815 | NEXN | c.1135G>T (p.Glu379Ter) c.943G>T (p.Glu315Ter) c.834G>T c.1093G>T (p.Glu365Ter) n.595G>T n.709G>T c.901G>T (p.Glu301Ter) c.718G>T (p.Glu240Ter) | |
1 | g.77933364A>C | CA340876829 | NEXN | c.1136A>C (p.Glu379Ala) c.944A>C (p.Glu315Ala) c.835A>C c.1094A>C (p.Glu365Ala) n.596A>C n.710A>C c.902A>C (p.Glu301Ala) c.719A>C (p.Glu240Ala) | |
1 | g.77933364A>G | CA340876830 | NEXN | c.1136A>G (p.Glu379Gly) c.944A>G (p.Glu315Gly) c.835A>G c.1094A>G (p.Glu365Gly) n.596A>G n.710A>G c.902A>G (p.Glu301Gly) c.719A>G (p.Glu240Gly) | |
1 | g.77933364A>T | CA340876832 | NEXN | c.1136A>T (p.Glu379Val) c.944A>T (p.Glu315Val) c.835A>T c.1094A>T (p.Glu365Val) n.596A>T n.710A>T c.902A>T (p.Glu301Val) c.719A>T (p.Glu240Val) | |
1 | g.77933365A= | CA1177626724 | NEXN | c.1137A= (p.Glu379=) c.945A= (p.Glu315=) c.836A= c.1095A= (p.Glu365=) n.597A= n.711A= c.903A= (p.Glu301=) c.720A= (p.Glu240=) | |
1 | g.77933365A>C | CA340876834 | NEXN | c.1137A>C (p.Glu379Asp) c.945A>C (p.Glu315Asp) c.836A>C c.1095A>C (p.Glu365Asp) n.597A>C n.711A>C c.903A>C (p.Glu301Asp) c.720A>C (p.Glu240Asp) | |
1 | g.77933365A>G | CA418572078 | NEXN | c.1137A>G (p.Glu379=) c.945A>G (p.Glu315=) c.836A>G c.1095A>G (p.Glu365=) n.597A>G n.711A>G c.903A>G (p.Glu301=) c.720A>G (p.Glu240=) | ClinVar dbSNP |
1 | g.77933365A>T | CA340876836 | NEXN | c.1137A>T (p.Glu379Asp) c.945A>T (p.Glu315Asp) c.836A>T c.1095A>T (p.Glu365Asp) n.597A>T n.711A>T c.903A>T (p.Glu301Asp) c.720A>T (p.Glu240Asp) | |
1 | g.77933366G>A | CA340876838 | NEXN | c.1138G>A (p.Glu380Lys) c.946G>A (p.Glu316Lys) c.837G>A c.1096G>A (p.Glu366Lys) n.598G>A n.712G>A c.904G>A (p.Glu302Lys) c.721G>A (p.Glu241Lys) | |
1 | g.77933366G>C | CA340876840 | NEXN | c.1138G>C (p.Glu380Gln) c.946G>C (p.Glu316Gln) c.837G>C c.1096G>C (p.Glu366Gln) n.598G>C n.712G>C c.904G>C (p.Glu302Gln) c.721G>C (p.Glu241Gln) | |
1 | g.77933366G>T | CA340876842 | NEXN | c.1138G>T (p.Glu380Ter) c.946G>T (p.Glu316Ter) c.837G>T c.1096G>T (p.Glu366Ter) n.598G>T n.712G>T c.904G>T (p.Glu302Ter) c.721G>T (p.Glu241Ter) | |
1 | g.77933366_77933369delinsGAAT | CA1177626725 | NEXN | c.1138_1141delinsGAAT (p.Glu380=) c.946_949delinsGAAT (p.Glu316=) c.837_840delinsGAAT c.1096_1099delinsGAAT (p.Glu366=) n.598_601delinsGAAT n.712_715delinsGAAT c.904_907delinsGAAT (p.Glu302=) c.721_724delinsGAAT (p.Glu241=) | |
1 | g.77933367A= | CA1177626728 | NEXN | c.1139A= (p.Glu380=) c.947A= (p.Glu316=) c.838A= c.1097A= (p.Glu366=) n.599A= n.713A= c.905A= (p.Glu302=) c.722A= (p.Glu241=) | |
1 | g.77933367A>C | CA340876843 | NEXN | c.1139A>C (p.Glu380Ala) c.947A>C (p.Glu316Ala) c.838A>C c.1097A>C (p.Glu366Ala) n.599A>C n.713A>C c.905A>C (p.Glu302Ala) c.722A>C (p.Glu241Ala) | |
1 | g.77933367A>G | CA340876846 | NEXN | c.1139A>G (p.Glu380Gly) c.947A>G (p.Glu316Gly) c.838A>G c.1097A>G (p.Glu366Gly) n.599A>G n.713A>G c.905A>G (p.Glu302Gly) c.722A>G (p.Glu241Gly) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.77933367A>T | CA340876852 | NEXN | c.1139A>T (p.Glu380Val) c.947A>T (p.Glu316Val) c.838A>T c.1097A>T (p.Glu366Val) n.599A>T n.713A>T c.905A>T (p.Glu302Val) c.722A>T (p.Glu241Val) | dbSNP gnomAD v4 |
1 | g.77933367_77933369del | CA1177626730 | NEXN | c.1139_1141del (p.Glu380_Leu381delinsVal) c.947_949del (p.Glu316_Leu317delinsVal) c.838_840del c.1097_1099del (p.Glu366_Leu367delinsVal) n.599_601del n.713_715del c.905_907del (p.Glu302_Leu303delinsVal) c.722_724del (p.Glu241_Leu242delinsVal) | dbSNP gnomAD v4 |
1 | g.77933368_77933371del | CA2574414089 | NEXN | c.1140_1143del (p.Glu380AspfsTer2) c.948_951del (p.Glu316AspfsTer2) c.839_842del c.1098_1101del (p.Glu366AspfsTer2) n.600_603del n.714_717del c.906_909del (p.Glu302AspfsTer2) c.723_726del (p.Glu241AspfsTer2) | gnomAD v4 |
1 | g.77933368A>C | CA340876853 | NEXN | c.1140A>C (p.Glu380Asp) c.948A>C (p.Glu316Asp) c.839A>C c.1098A>C (p.Glu366Asp) n.600A>C n.714A>C c.906A>C (p.Glu302Asp) c.723A>C (p.Glu241Asp) | |
1 | g.77933368A>G | CA418572079 | NEXN | c.1140A>G (p.Glu380=) c.948A>G (p.Glu316=) c.839A>G c.1098A>G (p.Glu366=) n.600A>G n.714A>G c.906A>G (p.Glu302=) c.723A>G (p.Glu241=) | ClinVar |
1 | g.77933368A>T | CA340876854 | NEXN | c.1140A>T (p.Glu380Asp) c.948A>T (p.Glu316Asp) c.839A>T c.1098A>T (p.Glu366Asp) n.600A>T n.714A>T c.906A>T (p.Glu302Asp) c.723A>T (p.Glu241Asp) | |
1 | g.77933372_77933374del | CA2646274520 | NEXN | c.1144_1146del (p.Leu382del) c.952_954del (p.Leu318del) c.843_845del c.1102_1104del (p.Leu368del) n.604_606del n.718_720del c.910_912del (p.Leu304del) c.727_729del (p.Leu243del) | gnomAD v4 |
1 | g.77933369T>A | CA340876855 | NEXN | c.1141T>A (p.Leu381Ile) c.949T>A (p.Leu317Ile) c.840T>A c.1099T>A (p.Leu367Ile) n.601T>A n.715T>A c.907T>A (p.Leu303Ile) c.724T>A (p.Leu242Ile) | |
1 | g.77933369T>C | CA418572080 | NEXN | c.1141T>C (p.Leu381=) c.949T>C (p.Leu317=) c.840T>C c.1099T>C (p.Leu367=) n.601T>C n.715T>C c.907T>C (p.Leu303=) c.724T>C (p.Leu242=) | |
1 | g.77933369T>G | CA340876856 | NEXN | c.1141T>G (p.Leu381Val) c.949T>G (p.Leu317Val) c.840T>G c.1099T>G (p.Leu367Val) n.601T>G n.715T>G c.907T>G (p.Leu303Val) c.724T>G (p.Leu242Val) | dbSNP gnomAD v4 |
1 | g.77933369T= | CA1177626731 | NEXN | c.1141T= (p.Leu381=) c.949T= (p.Leu317=) c.840T= c.1099T= (p.Leu367=) n.601T= n.715T= c.907T= (p.Leu303=) c.724T= (p.Leu242=) | |
1 | g.77933370T>A | CA340876857 | NEXN | c.1142T>A (p.Leu381Ter) c.950T>A (p.Leu317Ter) c.841T>A c.1100T>A (p.Leu367Ter) n.602T>A n.716T>A c.908T>A (p.Leu303Ter) c.725T>A (p.Leu242Ter) | |
1 | g.77933370T>C | CA340876858 | NEXN | c.1142T>C (p.Leu381Ser) c.950T>C (p.Leu317Ser) c.841T>C c.1100T>C (p.Leu367Ser) n.602T>C n.716T>C c.908T>C (p.Leu303Ser) c.725T>C (p.Leu242Ser) | |
1 | g.77933370T>G | CA340876860 | NEXN | c.1142T>G (p.Leu381Ter) c.950T>G (p.Leu317Ter) c.841T>G c.1100T>G (p.Leu367Ter) n.602T>G n.716T>G c.908T>G (p.Leu303Ter) c.725T>G (p.Leu242Ter) | |
1 | g.77933371A>C | CA340876864 | NEXN | c.1143A>C (p.Leu381Phe) c.951A>C (p.Leu317Phe) c.842A>C c.1101A>C (p.Leu367Phe) n.603A>C n.717A>C c.909A>C (p.Leu303Phe) c.726A>C (p.Leu242Phe) | |
1 | g.77933371A>G | CA418572081 | NEXN | c.1143A>G (p.Leu381=) c.951A>G (p.Leu317=) c.842A>G c.1101A>G (p.Leu367=) n.603A>G n.717A>G c.909A>G (p.Leu303=) c.726A>G (p.Leu242=) | gnomAD v4 |
1 | g.77933371A>T | CA340876867 | NEXN | c.1143A>T (p.Leu381Phe) c.951A>T (p.Leu317Phe) c.842A>T c.1101A>T (p.Leu367Phe) n.603A>T n.717A>T c.909A>T (p.Leu303Phe) c.726A>T (p.Leu242Phe) | ClinVar dbSNP |
1 | g.77933372T>A | CA340876870 | NEXN | c.1144T>A (p.Leu382Ile) c.952T>A (p.Leu318Ile) c.843T>A c.1102T>A (p.Leu368Ile) n.604T>A n.718T>A c.910T>A (p.Leu304Ile) c.727T>A (p.Leu243Ile) | |
1 | g.77933372T>C | CA418572082 | NEXN | c.1144T>C (p.Leu382=) c.952T>C (p.Leu318=) c.843T>C c.1102T>C (p.Leu368=) n.604T>C n.718T>C c.910T>C (p.Leu304=) c.727T>C (p.Leu243=) | ClinVar gnomAD v4 |
1 | g.77933372T>G | CA340876874 | NEXN | c.1144T>G (p.Leu382Val) c.952T>G (p.Leu318Val) c.843T>G c.1102T>G (p.Leu368Val) n.604T>G n.718T>G c.910T>G (p.Leu304Val) c.727T>G (p.Leu243Val) | |
1 | g.77933373T>A | CA340876876 | NEXN | c.1145T>A (p.Leu382Ter) c.953T>A (p.Leu318Ter) c.844T>A c.1103T>A (p.Leu368Ter) n.605T>A n.719T>A c.911T>A (p.Leu304Ter) c.728T>A (p.Leu243Ter) | |
1 | g.77933373T>C | CA340876878 | NEXN | c.1145T>C (p.Leu382Ser) c.953T>C (p.Leu318Ser) c.844T>C c.1103T>C (p.Leu368Ser) n.605T>C n.719T>C c.911T>C (p.Leu304Ser) c.728T>C (p.Leu243Ser) | |
1 | g.77933373T>G | CA340876879 | NEXN | c.1145T>G (p.Leu382Ter) c.953T>G (p.Leu318Ter) c.844T>G c.1103T>G (p.Leu368Ter) n.605T>G n.719T>G c.911T>G (p.Leu304Ter) c.728T>G (p.Leu243Ter) | |
1 | g.77933374A>C | CA340876881 | NEXN | c.1146A>C (p.Leu382Phe) c.954A>C (p.Leu318Phe) c.845A>C c.1104A>C (p.Leu368Phe) n.606A>C n.720A>C c.912A>C (p.Leu304Phe) c.729A>C (p.Leu243Phe) | |
1 | g.77933374A>G | CA418572083 | NEXN | c.1146A>G (p.Leu382=) c.954A>G (p.Leu318=) c.845A>G c.1104A>G (p.Leu368=) n.606A>G n.720A>G c.912A>G (p.Leu304=) c.729A>G (p.Leu243=) | |
1 | g.77933374A>T | CA340876882 | NEXN | c.1146A>T (p.Leu382Phe) c.954A>T (p.Leu318Phe) c.845A>T c.1104A>T (p.Leu368Phe) n.606A>T n.720A>T c.912A>T (p.Leu304Phe) c.729A>T (p.Leu243Phe) | |
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.77933375A>C | CA340876884 | NEXN | c.1147A>C (p.Lys383Gln) c.955A>C (p.Lys319Gln) c.846A>C c.1105A>C (p.Lys369Gln) n.607A>C n.721A>C c.913A>C (p.Lys305Gln) c.730A>C (p.Lys244Gln) | |
1 | g.77933375A>G | CA340876887 | NEXN | c.1147A>G (p.Lys383Glu) c.955A>G (p.Lys319Glu) c.846A>G c.1105A>G (p.Lys369Glu) n.607A>G n.721A>G c.913A>G (p.Lys305Glu) c.730A>G (p.Lys244Glu) | |
1 | g.77933375A>T | CA340876885 | NEXN | c.1147A>T (p.Lys383Ter) c.955A>T (p.Lys319Ter) c.846A>T c.1105A>T (p.Lys369Ter) n.607A>T n.721A>T c.913A>T (p.Lys305Ter) c.730A>T (p.Lys244Ter) | |
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) |