Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.41474507G>A | CA412992178 | NYX | c.1039G>A (p.Glu347Lys) c.1054G>A (p.Glu352Lys) | |
X | g.41474507G>C | CA412992179 | NYX | c.1039G>C (p.Glu347Gln) c.1054G>C (p.Glu352Gln) | |
X | g.41474507G>T | CA412992180 | NYX | c.1039G>T (p.Glu347Ter) c.1054G>T (p.Glu352Ter) | gnomAD v4 |
X | g.41474508del | CA2579588826 | NYX | c.1040del (p.Glu347GlyfsTer25) c.1055del (p.Glu352GlyfsTer25) | |
X | g.41474508A>C | CA412992181 | NYX | c.1040A>C (p.Glu347Ala) c.1055A>C (p.Glu352Ala) | |
X | g.41474508A>G | CA412992182 | NYX | c.1040A>G (p.Glu347Gly) c.1055A>G (p.Glu352Gly) | gnomAD v4 |
X | g.41474508A>T | CA412992183 | NYX | c.1040A>T (p.Glu347Val) c.1055A>T (p.Glu352Val) | |
X | g.41474509G>A | CA516366425 | NYX | c.1041G>A (p.Glu347=) c.1056G>A (p.Glu352=) | dbSNP gnomAD v2 gnomAD v4 |
X | g.41474509G>C | CA412992184 | NYX | c.1041G>C (p.Glu347Asp) c.1056G>C (p.Glu352Asp) | |
X | g.41474509G= | CA2425928098 | NYX | c.1041G= (p.Glu347=) c.1056G= (p.Glu352=) | |
X | g.41474509G>T | CA412992185 | NYX | c.1041G>T (p.Glu347Asp) c.1056G>T (p.Glu352Asp) | |
X | g.41474510G>A | CA412992188 | NYX | c.1042G>A (p.Gly348Ser) c.1057G>A (p.Gly353Ser) | ClinVar dbSNP |
X | g.41474510G>C | CA412992187 | NYX | c.1042G>C (p.Gly348Arg) c.1057G>C (p.Gly353Arg) | |
X | g.41474510G>T | CA412992186 | NYX | c.1042G>T (p.Gly348Cys) c.1057G>T (p.Gly353Cys) | gnomAD v4 |
X | g.41474511G>A | CA412992483 | NYX | c.1043G>A (p.Gly348Asp) c.1058G>A (p.Gly353Asp) | |
X | g.41474511G>C | CA412992484 | NYX | c.1043G>C (p.Gly348Ala) c.1058G>C (p.Gly353Ala) | |
X | g.41474511G>T | CA412992485 | NYX | c.1043G>T (p.Gly348Val) c.1058G>T (p.Gly353Val) | gnomAD v4 |
X | g.41474512C>A | CA516365876 | NYX | c.1044C>A (p.Gly348=) c.1059C>A (p.Gly353=) | |
X | g.41474512C>G | CA516365875 | NYX | c.1044C>G (p.Gly348=) c.1059C>G (p.Gly353=) | |
X | g.41474512C>T | CA516365874 | NYX | c.1044C>T (p.Gly348=) c.1059C>T (p.Gly353=) | |
X | g.41474513T>A | CA412992486 | NYX | c.1045T>A (p.Ser349Thr) c.1060T>A (p.Ser354Thr) | |
X | g.41474513T>C | CA412992487 | NYX | c.1045T>C (p.Ser349Pro) c.1060T>C (p.Ser354Pro) | |
X | g.41474513T>G | CA412992488 | NYX | c.1045T>G (p.Ser349Ala) c.1060T>G (p.Ser354Ala) | |
X | g.41474514C>A | CA412992489 | NYX | c.1046C>A (p.Ser349Tyr) c.1061C>A (p.Ser354Tyr) | gnomAD v4 |
X | g.41474514C>G | CA412992490 | NYX | c.1046C>G (p.Ser349Cys) c.1061C>G (p.Ser354Cys) | |
X | g.41474514C>T | CA412992491 | NYX | c.1046C>T (p.Ser349Phe) c.1061C>T (p.Ser354Phe) | COSMIC |
X | g.41474515C>A | CA516365879 | NYX | c.1047C>A (p.Ser349=) c.1062C>A (p.Ser354=) | gnomAD v4 |
X | g.41474515C= | CA2425928099 | NYX | c.1047C= (p.Ser349=) c.1062C= (p.Ser354=) | |
X | g.41474515C>G | CA516365880 | NYX | c.1047C>G (p.Ser349=) c.1062C>G (p.Ser354=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474515C>T | CA516365881 | NYX | c.1047C>T (p.Ser349=) c.1062C>T (p.Ser354=) | gnomAD v4 |
X | g.41474516G>A | CA10389901 | NYX | c.1048G>A (p.Gly350Arg) c.1063G>A (p.Gly355Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474516G>C | CA412992492 | NYX | c.1048G>C (p.Gly350Arg) c.1063G>C (p.Gly355Arg) | |
X | g.41474516G= | CA2425928100 | NYX | c.1048G= (p.Gly350=) c.1063G= (p.Gly355=) | |
X | g.41474516G>T | CA412992493 | NYX | c.1048G>T (p.Gly350Ter) c.1063G>T (p.Gly355Ter) | gnomAD v4 |
X | g.41474517G>A | CA412992496 | NYX | c.1049G>A (p.Gly350Glu) c.1064G>A (p.Gly355Glu) | |
X | g.41474517G>C | CA412992495 | NYX | c.1049G>C (p.Gly350Ala) c.1064G>C (p.Gly355Ala) | |
X | g.41474517G>T | CA412992494 | NYX | c.1049G>T (p.Gly350Val) c.1064G>T (p.Gly355Val) | gnomAD v4 |
X | g.41474518A>C | CA516365882 | NYX | c.1050A>C (p.Gly350=) c.1065A>C (p.Gly355=) | |
X | g.41474518A>G | CA516365884 | NYX | c.1050A>G (p.Gly350=) c.1065A>G (p.Gly355=) | gnomAD v4 |
X | g.41474518A>T | CA516365883 | NYX | c.1050A>T (p.Gly350=) c.1065A>T (p.Gly355=) | |
X | g.41474519C>A | CA412992497 | NYX | c.1051C>A (p.Arg351Ser) c.1066C>A (p.Arg356Ser) | |
X | g.41474519C= | CA2425928101 | NYX | c.1051C= (p.Arg351=) c.1066C= (p.Arg356=) | |
X | g.41474519C>G | CA412992498 | NYX | c.1051C>G (p.Arg351Gly) c.1066C>G (p.Arg356Gly) | dbSNP gnomAD v4 |
X | g.41474519C>T | CA10389902 | NYX | c.1051C>T (p.Arg351Cys) c.1066C>T (p.Arg356Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474519_41474521delinsCGT | CA2425928102 | NYX | c.1051_1053delinsCGT (p.Arg351=) c.1066_1068delinsCGT (p.Arg356=) | |
X | g.41474520G>A | CA412992499 | NYX | c.1052G>A (p.Arg351His) c.1067G>A (p.Arg356His) | gnomAD v4 |
X | g.41474520G>C | CA412992500 | NYX | c.1052G>C (p.Arg351Pro) c.1067G>C (p.Arg356Pro) | |
X | g.41474520G>T | CA412992501 | NYX | c.1052G>T (p.Arg351Leu) c.1067G>T (p.Arg356Leu) | |
X | g.41474522_41474523del | CA915951044 | NYX | c.1054_1055del (p.Val352HisfsTer?) c.1069_1070del (p.Val357HisfsTer?) | ClinVar dbSNP |
X | g.41474521T>A | CA516365885 | NYX | c.1053T>A (p.Arg351=) c.1068T>A (p.Arg356=) | |
X | g.41474521T>C | CA516365886 | NYX | c.1053T>C (p.Arg351=) c.1068T>C (p.Arg356=) | |
X | g.41474521T>G | CA516365887 | NYX | c.1053T>G (p.Arg351=) c.1068T>G (p.Arg356=) | |
X | g.41474522G>A | CA412992502 | NYX | c.1054G>A (p.Val352Ile) c.1069G>A (p.Val357Ile) | gnomAD v4 |
X | g.41474522G>C | CA412992503 | NYX | c.1054G>C (p.Val352Leu) c.1069G>C (p.Val357Leu) | |
X | g.41474522G>T | CA412992504 | NYX | c.1054G>T (p.Val352Phe) c.1069G>T (p.Val357Phe) | gnomAD v4 |
X | g.41474523del | CA2546103442 | NYX | c.1055del (p.Val352AlafsTer20) c.1070del (p.Val357AlafsTer20) | |
X | g.41474523T>A | CA412992505 | NYX | c.1055T>A (p.Val352Asp) c.1070T>A (p.Val357Asp) | |
X | g.41474523T>C | CA412992506 | NYX | c.1055T>C (p.Val352Ala) c.1070T>C (p.Val357Ala) | |
X | g.41474523T>G | CA412992507 | NYX | c.1055T>G (p.Val352Gly) c.1070T>G (p.Val357Gly) | |
X | g.41474524C>A | CA516365890 | NYX | c.1056C>A (p.Val352=) c.1071C>A (p.Val357=) | |
X | g.41474524C>G | CA516365892 | NYX | c.1056C>G (p.Val352=) c.1071C>G (p.Val357=) | |
X | g.41474524C>T | CA516365891 | NYX | c.1056C>T (p.Val352=) c.1071C>T (p.Val357=) | |
X | g.41474525A= | CA2425928103 | NYX | c.1057A= (p.Thr353=) c.1072A= (p.Thr358=) | |
X | g.41474525A>C | CA412992510 | NYX | c.1057A>C (p.Thr353Pro) c.1072A>C (p.Thr358Pro) | |
X | g.41474525A>G | CA412992508 | NYX | c.1057A>G (p.Thr353Ala) c.1072A>G (p.Thr358Ala) | dbSNP gnomAD v2 gnomAD v4 |
X | g.41474525A>T | CA412992509 | NYX | c.1057A>T (p.Thr353Ser) c.1072A>T (p.Thr358Ser) | |
X | g.41474525_41474526insG | CA2545649389 | NYX | c.1057_1058insG (p.Thr353SerfsTer?) c.1072_1073insG (p.Thr358SerfsTer?) | |
X | g.41474526C>A | CA412992512 | NYX | c.1058C>A (p.Thr353Asn) c.1073C>A (p.Thr358Asn) | |
X | g.41474526C= | CA2425928104 | NYX | c.1058C= (p.Thr353=) c.1073C= (p.Thr358=) | |
X | g.41474526C>G | CA412992514 | NYX | c.1058C>G (p.Thr353Ser) c.1073C>G (p.Thr358Ser) | gnomAD v4 |
X | g.41474526C>T | CA412992515 | NYX | c.1058C>T (p.Thr353Ile) c.1073C>T (p.Thr358Ile) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474527C>A | CA516365894 | NYX | c.1059C>A (p.Thr353=) c.1074C>A (p.Thr358=) | gnomAD v4 COSMIC |
X | g.41474527C= | CA2425928105 | NYX | c.1059C= (p.Thr353=) c.1074C= (p.Thr358=) | |
X | g.41474527C>G | CA516365895 | NYX | c.1059C>G (p.Thr353=) c.1074C>G (p.Thr358=) | |
X | g.41474527C>T | CA10389903 | NYX | c.1059C>T (p.Thr353=) c.1074C>T (p.Thr358=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474528G>A | CA412992518 | NYX | c.1060G>A (p.Asp354Asn) c.1075G>A (p.Asp359Asn) | gnomAD v4 |
X | g.41474528G>C | CA412992520 | NYX | c.1060G>C (p.Asp354His) c.1075G>C (p.Asp359His) | |
X | g.41474528G>T | CA412992522 | NYX | c.1060G>T (p.Asp354Tyr) c.1075G>T (p.Asp359Tyr) | |
X | g.41474529A>C | CA412992523 | NYX | c.1061A>C (p.Asp354Ala) c.1076A>C (p.Asp359Ala) | |
X | g.41474529A>G | CA412992525 | NYX | c.1061A>G (p.Asp354Gly) c.1076A>G (p.Asp359Gly) | |
X | g.41474529A>T | CA412992526 | NYX | c.1061A>T (p.Asp354Val) c.1076A>T (p.Asp359Val) | |
X | g.41474530C>A | CA412992528 | NYX | c.1062C>A (p.Asp354Glu) c.1077C>A (p.Asp359Glu) | |
X | g.41474530C= | CA2425928106 | NYX | c.1062C= (p.Asp354=) c.1077C= (p.Asp359=) | |
X | g.41474530C>G | CA412992529 | NYX | c.1062C>G (p.Asp354Glu) c.1077C>G (p.Asp359Glu) | dbSNP |
X | g.41474530C>T | CA516365897 | NYX | c.1062C>T (p.Asp354=) c.1077C>T (p.Asp359=) | dbSNP gnomAD v2 gnomAD v4 |
X | g.41474531G>A | CA10389904 | NYX | c.1063G>A (p.Val355Met) c.1078G>A (p.Val360Met) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.41474531G>C | CA412992534 | NYX | c.1063G>C (p.Val355Leu) c.1078G>C (p.Val360Leu) | |
X | g.41474531G= | CA2425928107 | NYX | c.1063G= (p.Val355=) c.1078G= (p.Val360=) | |
X | g.41474531G>T | CA412992532 | NYX | c.1063G>T (p.Val355Leu) c.1078G>T (p.Val360Leu) | |
X | g.41474532T>A | CA412992536 | NYX | c.1064T>A (p.Val355Glu) c.1079T>A (p.Val360Glu) | |
X | g.41474532T>C | CA412992538 | NYX | c.1064T>C (p.Val355Ala) c.1079T>C (p.Val360Ala) | |
X | g.41474532T>G | CA412992539 | NYX | c.1064T>G (p.Val355Gly) c.1079T>G (p.Val360Gly) | |
X | g.41474533G>A | CA516365903 | NYX | c.1065G>A (p.Val355=) c.1080G>A (p.Val360=) | gnomAD v4 |
X | g.41474533G>C | CA516365901 | NYX | c.1065G>C (p.Val355=) c.1080G>C (p.Val360=) | |
X | g.41474533G>T | CA516365902 | NYX | c.1065G>T (p.Val355=) c.1080G>T (p.Val360=) | |
X | g.41474534C>A | CA412992542 | NYX | c.1066C>A (p.Pro356Thr) c.1081C>A (p.Pro361Thr) | |
X | g.41474534C>G | CA412992543 | NYX | c.1066C>G (p.Pro356Ala) c.1081C>G (p.Pro361Ala) | |
X | g.41474534C>T | CA412992545 | NYX | c.1066C>T (p.Pro356Ser) c.1081C>T (p.Pro361Ser) | gnomAD v4 COSMIC |
X | g.41474535C>A | CA412992551 | NYX | c.1067C>A (p.Pro356Gln) c.1082C>A (p.Pro361Gln) | gnomAD v4 |
X | g.41474535C>G | CA412992547 | NYX | c.1067C>G (p.Pro356Arg) c.1082C>G (p.Pro361Arg) | |
X | g.41474535C>T | CA412992549 | NYX | c.1067C>T (p.Pro356Leu) c.1082C>T (p.Pro361Leu) | gnomAD v4 |
X | g.41474536G>A | CA516365907 | NYX | c.1068G>A (p.Pro356=) c.1083G>A (p.Pro361=) | gnomAD v4 |
X | g.41474536G>C | CA516365908 | NYX | c.1068G>C (p.Pro356=) c.1083G>C (p.Pro361=) | |
X | g.41474536G>T | CA516365909 | NYX | c.1068G>T (p.Pro356=) c.1083G>T (p.Pro361=) | gnomAD v4 |
X | g.41474537T>A | CA412992553 | NYX | c.1069T>A (p.Cys357Ser) c.1084T>A (p.Cys362Ser) | |
X | g.41474537T>C | CA412992555 | NYX | c.1069T>C (p.Cys357Arg) c.1084T>C (p.Cys362Arg) | |
X | g.41474537T>G | CA412992556 | NYX | c.1069T>G (p.Cys357Gly) c.1084T>G (p.Cys362Gly) | |
X | g.41474538G>A | CA412992558 | NYX | c.1070G>A (p.Cys357Tyr) c.1085G>A (p.Cys362Tyr) | |
X | g.41474538G>C | CA412992560 | NYX | c.1070G>C (p.Cys357Ser) c.1085G>C (p.Cys362Ser) | |
X | g.41474538G= | CA2425928108 | NYX | c.1070G= (p.Cys357=) c.1085G= (p.Cys362=) | |
X | g.41474538G>T | CA329217076 | NYX | c.1070G>T (p.Cys357Phe) c.1085G>T (p.Cys362Phe) | dbSNP gnomAD v4 COSMIC |
X | g.41474539del | CA2695233446 | NYX | c.1071del (p.Cys357TrpfsTer15) c.1086del (p.Cys362TrpfsTer15) | |
X | g.41474539C>A | CA412992563 | NYX | c.1071C>A (p.Cys357Ter) c.1086C>A (p.Cys362Ter) | ClinVar |
X | g.41474539C= | CA2425928109 | NYX | c.1071C= (p.Cys357=) c.1086C= (p.Cys362=) | |
X | g.41474539C>G | CA412992566 | NYX | c.1071C>G (p.Cys357Trp) c.1086C>G (p.Cys362Trp) | |
X | g.41474539C>T | CA10389905 | NYX | c.1071C>T (p.Cys357=) c.1086C>T (p.Cys362=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.41474540G>A | CA412992568 | NYX | c.1072G>A (p.Ala358Thr) c.1087G>A (p.Ala363Thr) | gnomAD v4 |
X | g.41474540G>C | CA412992570 | NYX | c.1072G>C (p.Ala358Pro) c.1087G>C (p.Ala363Pro) | |
X | g.41474540G= | CA2425928110 | NYX | c.1072G= (p.Ala358=) c.1087G= (p.Ala363=) | |
X | g.41474540G>T | CA412992572 | NYX | c.1072G>T (p.Ala358Ser) c.1087G>T (p.Ala363Ser) | dbSNP gnomAD v4 |
X | g.41474541C>A | CA412992574 | NYX | c.1073C>A (p.Ala358Asp) c.1088C>A (p.Ala363Asp) | |
X | g.41474541C= | CA2425928111 | NYX | c.1073C= (p.Ala358=) c.1088C= (p.Ala363=) | |
X | g.41474541C>G | CA412992576 | NYX | c.1073C>G (p.Ala358Gly) c.1088C>G (p.Ala363Gly) | gnomAD v4 |
X | g.41474541C>T | CA412992578 | NYX | c.1073C>T (p.Ala358Val) c.1088C>T (p.Ala363Val) | dbSNP gnomAD v2 gnomAD v4 |
X | g.41474542C>A | CA516365915 | NYX | c.1074C>A (p.Ala358=) c.1089C>A (p.Ala363=) | gnomAD v4 |
X | g.41474542C>G | CA516365916 | NYX | c.1074C>G (p.Ala358=) c.1089C>G (p.Ala363=) | |
X | g.41474542C>T | CA516365917 | NYX | c.1074C>T (p.Ala358=) c.1089C>T (p.Ala363=) | |
X | g.41474543T>A | CA412992580 | NYX | c.1075T>A (p.Ser359Thr) c.1090T>A (p.Ser364Thr) | |
X | g.41474543T>C | CA412992582 | NYX | c.1075T>C (p.Ser359Pro) c.1090T>C (p.Ser364Pro) | gnomAD v4 |
X | g.41474543T>G | CA412992583 | NYX | c.1075T>G (p.Ser359Ala) c.1090T>G (p.Ser364Ala) | |
X | g.41474544C>A | CA10389906 | NYX | c.1076C>A (p.Ser359Tyr) c.1091C>A (p.Ser364Tyr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.41474544C= | CA2425928112 | NYX | c.1076C= (p.Ser359=) c.1091C= (p.Ser364=) | |
X | g.41474544C>G | CA412992586 | NYX | c.1076C>G (p.Ser359Cys) c.1091C>G (p.Ser364Cys) | |
X | g.41474544C>T | CA10389907 | NYX | c.1076C>T (p.Ser359Phe) c.1091C>T (p.Ser364Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474547del | CA645612109 | NYX | c.1079del (p.Pro360ArgfsTer12) c.1094del (p.Pro365ArgfsTer12) | gnomAD v4 COSMIC |
X | g.41474545C>A | CA516365921 | NYX | c.1077C>A (p.Ser359=) c.1092C>A (p.Ser364=) | |
X | g.41474545C= | CA2425928113 | NYX | c.1077C= (p.Ser359=) c.1092C= (p.Ser364=) | |
X | g.41474545C>G | CA516365922 | NYX | c.1077C>G (p.Ser359=) c.1092C>G (p.Ser364=) | |
X | g.41474545C>T | CA516365924 | NYX | c.1077C>T (p.Ser359=) c.1092C>T (p.Ser364=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474546C>A | CA412992589 | NYX | c.1078C>A (p.Pro360Thr) c.1093C>A (p.Pro365Thr) | gnomAD v4 |
X | g.41474546C= | CA2425928114 | NYX | c.1078C= (p.Pro360=) c.1093C= (p.Pro365=) | |
X | g.41474546C>G | CA412992593 | NYX | c.1078C>G (p.Pro360Ala) c.1093C>G (p.Pro365Ala) | |
X | g.41474546C>T | CA412992591 | NYX | c.1078C>T (p.Pro360Ser) c.1093C>T (p.Pro365Ser) | ClinVar dbSNP |
X | g.41474547C>A | CA412992595 | NYX | c.1079C>A (p.Pro360Gln) c.1094C>A (p.Pro365Gln) | gnomAD v4 |
X | g.41474547C>G | CA412992597 | NYX | c.1079C>G (p.Pro360Arg) c.1094C>G (p.Pro365Arg) | gnomAD v4 |
X | g.41474547C>T | CA412992598 | NYX | c.1079C>T (p.Pro360Leu) c.1094C>T (p.Pro365Leu) | gnomAD v4 COSMIC |
X | g.41474548G>A | CA329217077 | NYX | c.1080G>A (p.Pro360=) c.1095G>A (p.Pro365=) | dbSNP gnomAD v2 gnomAD v4 |
X | g.41474548G>C | CA516365932 | NYX | c.1080G>C (p.Pro360=) c.1095G>C (p.Pro365=) | |
X | g.41474548G= | CA2425928115 | NYX | c.1080G= (p.Pro360=) c.1095G= (p.Pro365=) | |
X | g.41474548G>T | CA516365933 | NYX | c.1080G>T (p.Pro360=) c.1095G>T (p.Pro365=) | ClinVar gnomAD v4 |
X | g.41474549G>A | CA412992599 | NYX | c.1081G>A (p.Gly361Ser) c.1096G>A (p.Gly366Ser) | |
X | g.41474549G>C | CA329217078 | NYX | c.1081G>C (p.Gly361Arg) c.1096G>C (p.Gly366Arg) | dbSNP gnomAD v2 gnomAD v4 |
X | g.41474549G= | CA2425928116 | NYX | c.1081G= (p.Gly361=) c.1096G= (p.Gly366=) | |
X | g.41474549G>T | CA412992602 | NYX | c.1081G>T (p.Gly361Cys) c.1096G>T (p.Gly366Cys) | gnomAD v4 |
X | g.41474550G>A | CA412992604 | NYX | c.1082G>A (p.Gly361Asp) c.1097G>A (p.Gly366Asp) | dbSNP gnomAD v2 gnomAD v4 |
X | g.41474550G>C | CA412992605 | NYX | c.1082G>C (p.Gly361Ala) c.1097G>C (p.Gly366Ala) | dbSNP gnomAD v3 gnomAD v4 |
X | g.41474550G= | CA2425928117 | NYX | c.1082G= (p.Gly361=) c.1097G= (p.Gly366=) | |
X | g.41474550G>T | CA412992607 | NYX | c.1082G>T (p.Gly361Val) c.1097G>T (p.Gly366Val) | gnomAD v4 |
X | g.41474551C>A | CA516365938 | NYX | c.1083C>A (p.Gly361=) c.1098C>A (p.Gly366=) | |
X | g.41474551C= | CA2425928118 | NYX | c.1083C= (p.Gly361=) c.1098C= (p.Gly366=) | |
X | g.41474551C>G | CA516365940 | NYX | c.1083C>G (p.Gly361=) c.1098C>G (p.Gly366=) | dbSNP gnomAD v2 gnomAD v4 |
X | g.41474551C>T | CA516365941 | NYX | c.1083C>T (p.Gly361=) c.1098C>T (p.Gly366=) | ClinVar |
X | g.41474552T>A | CA412992610 | NYX | c.1084T>A (p.Ser362Thr) c.1099T>A (p.Ser367Thr) | |
X | g.41474552T>C | CA412992611 | NYX | c.1084T>C (p.Ser362Pro) c.1099T>C (p.Ser367Pro) | |
X | g.41474552T>G | CA412992613 | NYX | c.1084T>G (p.Ser362Ala) c.1099T>G (p.Ser367Ala) | |
X | g.41474553C>A | CA412992618 | NYX | c.1085C>A (p.Ser362Tyr) c.1100C>A (p.Ser367Tyr) | gnomAD v4 |
X | g.41474553C>G | CA412992617 | NYX | c.1085C>G (p.Ser362Cys) c.1100C>G (p.Ser367Cys) | |
X | g.41474553C>T | CA412992615 | NYX | c.1085C>T (p.Ser362Phe) c.1100C>T (p.Ser367Phe) | |
X | g.41474554C>A | CA516365946 | NYX | c.1086C>A (p.Ser362=) c.1101C>A (p.Ser367=) | gnomAD v4 |
X | g.41474554C= | CA2425928119 | NYX | c.1086C= (p.Ser362=) c.1101C= (p.Ser367=) | |
X | g.41474554C>G | CA516365945 | NYX | c.1086C>G (p.Ser362=) c.1101C>G (p.Ser367=) | |
X | g.41474554C>T | CA10389908 | NYX | c.1086C>T (p.Ser362=) c.1101C>T (p.Ser367=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474555G>A | CA329217079 | NYX | c.1087G>A (p.Val363Met) c.1102G>A (p.Val368Met) | dbSNP gnomAD v4 |
X | g.41474555G>C | CA412992621 | NYX | c.1087G>C (p.Val363Leu) c.1102G>C (p.Val368Leu) | |
X | g.41474555G= | CA2425928120 | NYX | c.1087G= (p.Val363=) c.1102G= (p.Val368=) | |
X | g.41474555G>T | CA412992622 | NYX | c.1087G>T (p.Val363Leu) c.1102G>T (p.Val368Leu) | gnomAD v4 |
X | g.41474556T>A | CA412992624 | NYX | c.1088T>A (p.Val363Glu) c.1103T>A (p.Val368Glu) | ClinVar |
X | g.41474556T>C | CA412992626 | NYX | c.1088T>C (p.Val363Ala) c.1103T>C (p.Val368Ala) | |
X | g.41474556T>G | CA412992628 | NYX | c.1088T>G (p.Val363Gly) c.1103T>G (p.Val368Gly) | |
X | g.41474557G>A | CA516365952 | NYX | c.1089G>A (p.Val363=) c.1104G>A (p.Val368=) | |
X | g.41474557G>C | CA516365953 | NYX | c.1089G>C (p.Val363=) c.1104G>C (p.Val368=) | |
X | g.41474557G>T | CA516365955 | NYX | c.1089G>T (p.Val363=) c.1104G>T (p.Val368=) | |
X | g.41474558G>A | CA412992630 | NYX | c.1090G>A (p.Ala364Thr) c.1105G>A (p.Ala369Thr) | gnomAD v4 |
X | g.41474558G>C | CA412992632 | NYX | c.1090G>C (p.Ala364Pro) c.1105G>C (p.Ala369Pro) | |
X | g.41474558G>T | CA412992633 | NYX | c.1090G>T (p.Ala364Ser) c.1105G>T (p.Ala369Ser) | |
X | g.41474559C>A | CA412992636 | NYX | c.1091C>A (p.Ala364Asp) c.1106C>A (p.Ala369Asp) | gnomAD v4 |
X | g.41474559C>G | CA412992637 | NYX | c.1091C>G (p.Ala364Gly) c.1106C>G (p.Ala369Gly) | |
X | g.41474559C>T | CA412992638 | NYX | c.1091C>T (p.Ala364Val) c.1106C>T (p.Ala369Val) | gnomAD v4 |
X | g.41474560C>A | CA516365958 | NYX | c.1092C>A (p.Ala364=) c.1107C>A (p.Ala369=) | |
X | g.41474560C= | CA2425928121 | NYX | c.1092C= (p.Ala364=) c.1107C= (p.Ala369=) | |
X | g.41474560C>G | CA516365961 | NYX | c.1092C>G (p.Ala364=) c.1107C>G (p.Ala369=) | |
X | g.41474560C>T | CA516365959 | NYX | c.1092C>T (p.Ala364=) c.1107C>T (p.Ala369=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
X | g.41474561G>A | CA412992643 | NYX | c.1093G>A (p.Gly365Ser) c.1108G>A (p.Gly370Ser) | gnomAD v4 COSMIC |
X | g.41474561G>C | CA412992644 | NYX | c.1093G>C (p.Gly365Arg) c.1108G>C (p.Gly370Arg) | |
X | g.41474561G>T | CA412992641 | NYX | c.1093G>T (p.Gly365Cys) c.1108G>T (p.Gly370Cys) | gnomAD v4 |
X | g.41474562G>A | CA412992646 | NYX | c.1094G>A (p.Gly365Asp) c.1109G>A (p.Gly370Asp) | gnomAD v4 |
X | g.41474562G>C | CA412992647 | NYX | c.1094G>C (p.Gly365Ala) c.1109G>C (p.Gly370Ala) | |
X | g.41474562G= | CA2425928122 | NYX | c.1094G= (p.Gly365=) c.1109G= (p.Gly370=) | |
X | g.41474562G>T | CA227938 | NYX | c.1094G>T (p.Gly365Val) c.1109G>T (p.Gly370Val) | ClinVar dbSNP gnomAD v4 |
X | g.41474563C>A | CA516365968 | NYX | c.1095C>A (p.Gly365=) c.1110C>A (p.Gly370=) | gnomAD v4 |
X | g.41474563C= | CA2425928123 | NYX | c.1095C= (p.Gly365=) c.1110C= (p.Gly370=) | |
X | g.41474563C>G | CA516365966 | NYX | c.1095C>G (p.Gly365=) c.1110C>G (p.Gly370=) | |
X | g.41474563C>T | CA516365964 | NYX | c.1095C>T (p.Gly365=) c.1110C>T (p.Gly370=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474564C>A | CA412992650 | NYX | c.1096C>A (p.Leu366Met) c.1111C>A (p.Leu371Met) | gnomAD v4 |
X | g.41474564C= | CA2425928124 | NYX | c.1096C= (p.Leu366=) c.1111C= (p.Leu371=) | |
X | g.41474564C>G | CA412992652 | NYX | c.1096C>G (p.Leu366Val) c.1111C>G (p.Leu371Val) | |
X | g.41474564C>T | CA10389909 | NYX | c.1096C>T (p.Leu366=) c.1111C>T (p.Leu371=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474565T>A | CA412992655 | NYX | c.1097T>A (p.Leu366Gln) c.1112T>A (p.Leu371Gln) | gnomAD v4 |
X | g.41474565T>C | CA412992656 | NYX | c.1097T>C (p.Leu366Pro) c.1112T>C (p.Leu371Pro) | gnomAD v4 |
X | g.41474565T>G | CA412992658 | NYX | c.1097T>G (p.Leu366Arg) c.1112T>G (p.Leu371Arg) | |
X | g.41474566G>A | CA516365971 | NYX | c.1098G>A (p.Leu366=) c.1113G>A (p.Leu371=) | |
X | g.41474566G>C | CA516365975 | NYX | c.1098G>C (p.Leu366=) c.1113G>C (p.Leu371=) | gnomAD v4 |
X | g.41474566G>T | CA516365972 | NYX | c.1098G>T (p.Leu366=) c.1113G>T (p.Leu371=) | gnomAD v4 |
X | g.41474567G>A | CA412992661 | NYX | c.1099G>A (p.Asp367Asn) c.1114G>A (p.Asp372Asn) | gnomAD v4 |
X | g.41474567G>C | CA412992662 | NYX | c.1099G>C (p.Asp367His) c.1114G>C (p.Asp372His) | |
X | g.41474567G>T | CA412992663 | NYX | c.1099G>T (p.Asp367Tyr) c.1114G>T (p.Asp372Tyr) | gnomAD v4 |
X | g.41474568A>C | CA412992666 | NYX | c.1100A>C (p.Asp367Ala) c.1115A>C (p.Asp372Ala) | |
X | g.41474568A>G | CA412992667 | NYX | c.1100A>G (p.Asp367Gly) c.1115A>G (p.Asp372Gly) | |
X | g.41474568A>T | CA412992668 | NYX | c.1100A>T (p.Asp367Val) c.1115A>T (p.Asp372Val) | |
X | g.41474569C>A | CA412992670 | NYX | c.1101C>A (p.Asp367Glu) c.1116C>A (p.Asp372Glu) | |
X | g.41474569C>G | CA412992671 | NYX | c.1101C>G (p.Asp367Glu) c.1116C>G (p.Asp372Glu) | |
X | g.41474569C>T | CA516365979 | NYX | c.1101C>T (p.Asp367=) c.1116C>T (p.Asp372=) | |
X | g.41474570C>A | CA412992674 | NYX | c.1102C>A (p.Leu368Ile) c.1117C>A (p.Leu373Ile) | gnomAD v4 |
X | g.41474570C>G | CA412992676 | NYX | c.1102C>G (p.Leu368Val) c.1117C>G (p.Leu373Val) | |
X | g.41474570C>T | CA412992686 | NYX | c.1102C>T (p.Leu368Phe) c.1117C>T (p.Leu373Phe) | |
X | g.41474571T>A | CA412992688 | NYX | c.1103T>A (p.Leu368His) c.1118T>A (p.Leu373His) | |
X | g.41474571T>C | CA412992690 | NYX | c.1103T>C (p.Leu368Pro) c.1118T>C (p.Leu373Pro) | gnomAD v4 |
X | g.41474571T>G | CA412992692 | NYX | c.1103T>G (p.Leu368Arg) c.1118T>G (p.Leu373Arg) | |
X | g.41474572C>A | CA516365983 | NYX | c.1104C>A (p.Leu368=) c.1119C>A (p.Leu373=) | |
X | g.41474572C>G | CA516365985 | NYX | c.1104C>G (p.Leu368=) c.1119C>G (p.Leu373=) | |
X | g.41474572C>T | CA516365987 | NYX | c.1104C>T (p.Leu368=) c.1119C>T (p.Leu373=) | |
X | g.41474573A>C | CA412992697 | NYX | c.1105A>C (p.Ser369Arg) c.1120A>C (p.Ser374Arg) | |
X | g.41474573A>G | CA412992694 | NYX | c.1105A>G (p.Ser369Gly) c.1120A>G (p.Ser374Gly) | gnomAD v4 |
X | g.41474573A>T | CA412992696 | NYX | c.1105A>T (p.Ser369Cys) c.1120A>T (p.Ser374Cys) | |
X | g.41474575_41474910del | CA2573050969 | NYX | c.1107_*11del (n.[c.1107_*11del;Ser369ArgfsTer10]) c.1122_*11del (n.[c.1122_*11del;Ser374ArgfsTer10]) | |
X | g.41474574G>A | CA412992699 | NYX | c.1106G>A (p.Ser369Asn) c.1121G>A (p.Ser374Asn) | gnomAD v4 |
X | g.41474574G>C | CA412992700 | NYX | c.1106G>C (p.Ser369Thr) c.1121G>C (p.Ser374Thr) | |
X | g.41474574G>T | CA412992702 | NYX | c.1106G>T (p.Ser369Ile) c.1121G>T (p.Ser374Ile) | gnomAD v4 |
X | g.41474575C>A | CA412992704 | NYX | c.1107C>A (p.Ser369Arg) c.1122C>A (p.Ser374Arg) | gnomAD v4 |
X | g.41474575C= | CA2425928125 | NYX | c.1107C= (p.Ser369=) c.1122C= (p.Ser374=) | |
X | g.41474575C>G | CA412992705 | NYX | c.1107C>G (p.Ser369Arg) c.1122C>G (p.Ser374Arg) | |
X | g.41474575C>T | CA516365994 | NYX | c.1107C>T (p.Ser369=) c.1122C>T (p.Ser374=) | ClinVar dbSNP gnomAD v4 |
X | g.41474576C>A | CA412992708 | NYX | c.1108C>A (p.Gln370Lys) c.1123C>A (p.Gln375Lys) | gnomAD v4 |
X | g.41474576C= | CA2425928126 | NYX | c.1108C= (p.Gln370=) c.1123C= (p.Gln375=) | |
X | g.41474576C>G | CA412992711 | NYX | c.1108C>G (p.Gln370Glu) c.1123C>G (p.Gln375Glu) | |
X | g.41474576C>T | CA412992709 | NYX | c.1108C>T (p.Gln370Ter) c.1123C>T (p.Gln375Ter) | dbSNP gnomAD v2 gnomAD v4 |
X | g.41474577A>C | CA412992713 | NYX | c.1109A>C (p.Gln370Pro) c.1124A>C (p.Gln375Pro) | |
X | g.41474577A>G | CA412992715 | NYX | c.1109A>G (p.Gln370Arg) c.1124A>G (p.Gln375Arg) | |
X | g.41474577A>T | CA412992717 | NYX | c.1109A>T (p.Gln370Leu) c.1124A>T (p.Gln375Leu) | |
X | g.41474578G>A | CA516365999 | NYX | c.1110G>A (p.Gln370=) c.1125G>A (p.Gln375=) | |
X | g.41474578G>C | CA412992719 | NYX | c.1110G>C (p.Gln370His) c.1125G>C (p.Gln375His) | |
X | g.41474578G>T | CA412992721 | NYX | c.1110G>T (p.Gln370His) c.1125G>T (p.Gln375His) | gnomAD v4 |
X | g.41474579del | CA2568781542 | NYX | c.1111del (p.Val371Ter) c.1126del (p.Val376Ter) | |
X | g.41474579G>A | CA412992727 | NYX | c.1111G>A (p.Val371Met) c.1126G>A (p.Val376Met) | gnomAD v4 |
X | g.41474579G>C | CA412992725 | NYX | c.1111G>C (p.Val371Leu) c.1126G>C (p.Val376Leu) | |
X | g.41474579G>T | CA412992723 | NYX | c.1111G>T (p.Val371Leu) c.1126G>T (p.Val376Leu) | gnomAD v4 |
X | g.41474580T>A | CA412992728 | NYX | c.1112T>A (p.Val371Glu) c.1127T>A (p.Val376Glu) | |
X | g.41474580T>C | CA412992730 | NYX | c.1112T>C (p.Val371Ala) c.1127T>C (p.Val376Ala) | |
X | g.41474580T>G | CA412992732 | NYX | c.1112T>G (p.Val371Gly) c.1127T>G (p.Val376Gly) | |
X | g.41474581G>A | CA516366009 | NYX | c.1113G>A (p.Val371=) c.1128G>A (p.Val376=) | |
X | g.41474581G>C | CA516366011 | NYX | c.1113G>C (p.Val371=) c.1128G>C (p.Val376=) | |
X | g.41474581G>T | CA516366010 | NYX | c.1113G>T (p.Val371=) c.1128G>T (p.Val376=) | gnomAD v4 |
X | g.41474582A>C | CA412992734 | NYX | c.1114A>C (p.Thr372Pro) c.1129A>C (p.Thr377Pro) | |
X | g.41474582A>G | CA412992736 | NYX | c.1114A>G (p.Thr372Ala) c.1129A>G (p.Thr377Ala) | |
X | g.41474582A>T | CA412992738 | NYX | c.1114A>T (p.Thr372Ser) c.1129A>T (p.Thr377Ser) | |
X | g.41474583C>A | CA412992740 | NYX | c.1115C>A (p.Thr372Asn) c.1130C>A (p.Thr377Asn) | ClinVar |
X | g.41474583C>G | CA412992744 | NYX | c.1115C>G (p.Thr372Ser) c.1130C>G (p.Thr377Ser) | |
X | g.41474583C>T | CA412992742 | NYX | c.1115C>T (p.Thr372Ile) c.1130C>T (p.Thr377Ile) | |
X | g.41474584C>A | CA516366014 | NYX | c.1116C>A (p.Thr372=) c.1131C>A (p.Thr377=) | |
X | g.41474584C= | CA2425928127 | NYX | c.1116C= (p.Thr372=) c.1131C= (p.Thr377=) | |
X | g.41474584C>G | CA516366015 | NYX | c.1116C>G (p.Thr372=) c.1131C>G (p.Thr377=) | |
X | g.41474584C>T | CA516366017 | NYX | c.1116C>T (p.Thr372=) c.1131C>T (p.Thr377=) | dbSNP gnomAD v2 gnomAD v4 |
X | g.41474585T>A | CA412992746 | NYX | c.1117T>A (p.Phe373Ile) c.1132T>A (p.Phe378Ile) | |
X | g.41474585T>C | CA412992748 | NYX | c.1117T>C (p.Phe373Leu) c.1132T>C (p.Phe378Leu) | dbSNP |
X | g.41474585T>G | CA412992750 | NYX | c.1117T>G (p.Phe373Val) c.1132T>G (p.Phe378Val) | |
X | g.41474586T>A | CA412992752 | NYX | c.1118T>A (p.Phe373Tyr) c.1133T>A (p.Phe378Tyr) | |
X | g.41474586T>C | CA412992754 | NYX | c.1118T>C (p.Phe373Ser) c.1133T>C (p.Phe378Ser) | |
X | g.41474586T>G | CA412992755 | NYX | c.1118T>G (p.Phe373Cys) c.1133T>G (p.Phe378Cys) | dbSNP |
X | g.41474586T= | CA2425928128 | NYX | c.1118T= (p.Phe373=) c.1133T= (p.Phe378=) | |
X | g.41474587C>A | CA412992757 | NYX | c.1119C>A (p.Phe373Leu) c.1134C>A (p.Phe378Leu) | gnomAD v4 |
X | g.41474587C= | CA2425928129 | NYX | c.1119C= (p.Phe373=) c.1134C= (p.Phe378=) | |
X | g.41474587C>G | CA412992759 | NYX | c.1119C>G (p.Phe373Leu) c.1134C>G (p.Phe378Leu) | |
X | g.41474587C>T | CA516366024 | NYX | c.1119C>T (p.Phe373=) c.1134C>T (p.Phe378=) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
X | g.41474588G>A | CA412992762 | NYX | c.1120G>A (p.Gly374Arg) c.1135G>A (p.Gly379Arg) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
X | g.41474588G>C | CA412992763 | NYX | c.1120G>C (p.Gly374Arg) c.1135G>C (p.Gly379Arg) | |
X | g.41474588G= | CA2425928130 | NYX | c.1120G= (p.Gly374=) c.1135G= (p.Gly379=) | |
X | g.41474588G>T | CA412992764 | NYX | c.1120G>T (p.Gly374Trp) c.1135G>T (p.Gly379Trp) | gnomAD v4 |
X | g.41474589G>A | CA329217080 | NYX | c.1121G>A (p.Gly374Glu) c.1136G>A (p.Gly379Glu) | dbSNP |
X | g.41474589G>C | CA412992767 | NYX | c.1121G>C (p.Gly374Ala) c.1136G>C (p.Gly379Ala) | |
X | g.41474589G= | CA2425928131 | NYX | c.1121G= (p.Gly374=) c.1136G= (p.Gly379=) | |
X | g.41474589G>T | CA412992768 | NYX | c.1121G>T (p.Gly374Val) c.1136G>T (p.Gly379Val) | gnomAD v4 |
X | g.41474590G>A | CA516366031 | NYX | c.1122G>A (p.Gly374=) c.1137G>A (p.Gly379=) | gnomAD v4 |
X | g.41474590G>C | CA516366032 | NYX | c.1122G>C (p.Gly374=) c.1137G>C (p.Gly379=) | |
X | g.41474590G>T | CA516366034 | NYX | c.1122G>T (p.Gly374=) c.1137G>T (p.Gly379=) | |
X | g.41474591C>A | CA412992772 | NYX | c.1123C>A (p.Arg375Ser) c.1138C>A (p.Arg380Ser) | |
X | g.41474591C= | CA2425928132 | NYX | c.1123C= (p.Arg375=) c.1138C= (p.Arg380=) | |
X | g.41474591C>G | CA412992775 | NYX | c.1123C>G (p.Arg375Gly) c.1138C>G (p.Arg380Gly) | |
X | g.41474591C>T | CA412992773 | NYX | c.1123C>T (p.Arg375Cys) c.1138C>T (p.Arg380Cys) | dbSNP gnomAD v4 |
X | g.41474592G>A | CA10389910 | NYX | c.1124G>A (p.Arg375His) c.1139G>A (p.Arg380His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474592G>C | CA412992778 | NYX | c.1124G>C (p.Arg375Pro) c.1139G>C (p.Arg380Pro) | |
X | g.41474592G= | CA2425928133 | NYX | c.1124G= (p.Arg375=) c.1139G= (p.Arg380=) | |
X | g.41474592G>T | CA412992779 | NYX | c.1124G>T (p.Arg375Leu) c.1139G>T (p.Arg380Leu) | gnomAD v4 |
X | g.41474593C>A | CA516366043 | NYX | c.1125C>A (p.Arg375=) c.1140C>A (p.Arg380=) | gnomAD v4 |
X | g.41474593C>G | CA516366045 | NYX | c.1125C>G (p.Arg375=) c.1140C>G (p.Arg380=) | |
X | g.41474593C>T | CA516366046 | NYX | c.1125C>T (p.Arg375=) c.1140C>T (p.Arg380=) | |
X | g.41474594T>A | CA412992782 | NYX | c.1126T>A (p.Ser376Thr) c.1141T>A (p.Ser381Thr) | |
X | g.41474594T>C | CA10389911 | NYX | c.1126T>C (p.Ser376Pro) c.1141T>C (p.Ser381Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.41474594T>G | CA412992784 | NYX | c.1126T>G (p.Ser376Ala) c.1141T>G (p.Ser381Ala) | |
X | g.41474594T= | CA2425928134 | NYX | c.1126T= (p.Ser376=) c.1141T= (p.Ser381=) | |
X | g.41474595C>A | CA412992787 | NYX | c.1127C>A (p.Ser376Tyr) c.1142C>A (p.Ser381Tyr) | |
X | g.41474595C>G | CA412992788 | NYX | c.1127C>G (p.Ser376Cys) c.1142C>G (p.Ser381Cys) | |
X | g.41474595C>T | CA412992789 | NYX | c.1127C>T (p.Ser376Phe) c.1142C>T (p.Ser381Phe) | gnomAD v4 |
X | g.41474596C>A | CA516366058 | NYX | c.1128C>A (p.Ser376=) c.1143C>A (p.Ser381=) | |
X | g.41474596C>G | CA516366055 | NYX | c.1128C>G (p.Ser376=) c.1143C>G (p.Ser381=) | |
X | g.41474596C>T | CA516366057 | NYX | c.1128C>T (p.Ser376=) c.1143C>T (p.Ser381=) | |
X | g.41474597T>A | CA412992791 | NYX | c.1129T>A (p.Ser377Thr) c.1144T>A (p.Ser382Thr) | |
X | g.41474597T>C | CA412992793 | NYX | c.1129T>C (p.Ser377Pro) c.1144T>C (p.Ser382Pro) | |
X | g.41474597T>G | CA412992794 | NYX | c.1129T>G (p.Ser377Ala) c.1144T>G (p.Ser382Ala) | |
X | g.41474598C>A | CA412992805 | NYX | c.1130C>A (p.Ser377Tyr) c.1145C>A (p.Ser382Tyr) | gnomAD v4 |
X | g.41474598C= | CA2425928135 | NYX | c.1130C= (p.Ser377=) c.1145C= (p.Ser382=) | |
X | g.41474598C>G | CA412992797 | NYX | c.1130C>G (p.Ser377Cys) c.1145C>G (p.Ser382Cys) | dbSNP |
X | g.41474598C>T | CA412992804 | NYX | c.1130C>T (p.Ser377Phe) c.1145C>T (p.Ser382Phe) | COSMIC |
X | g.41474599C>A | CA516366063 | NYX | c.1131C>A (p.Ser377=) c.1146C>A (p.Ser382=) | gnomAD v4 |
X | g.41474599C>G | CA516366064 | NYX | c.1131C>G (p.Ser377=) c.1146C>G (p.Ser382=) | |
X | g.41474599C>T | CA516366065 | NYX | c.1131C>T (p.Ser377=) c.1146C>T (p.Ser382=) | gnomAD v4 |
X | g.41474600G>A | CA10389912 | NYX | c.1132G>A (p.Asp378Asn) c.1147G>A (p.Asp383Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474600G>C | CA412992808 | NYX | c.1132G>C (p.Asp378His) c.1147G>C (p.Asp383His) | gnomAD v4 |
X | g.41474600G= | CA2425928136 | NYX | c.1132G= (p.Asp378=) c.1147G= (p.Asp383=) | |
X | g.41474600G>T | CA412992810 | NYX | c.1132G>T (p.Asp378Tyr) c.1147G>T (p.Asp383Tyr) | gnomAD v4 |
X | g.41474601A>C | CA412992812 | NYX | c.1133A>C (p.Asp378Ala) c.1148A>C (p.Asp383Ala) | ClinVar |
X | g.41474601A>G | CA412992814 | NYX | c.1133A>G (p.Asp378Gly) c.1148A>G (p.Asp383Gly) | |
X | g.41474601A>T | CA412992815 | NYX | c.1133A>T (p.Asp378Val) c.1148A>T (p.Asp383Val) | gnomAD v4 |
X | g.41474602T>A | CA412992818 | NYX | c.1134T>A (p.Asp378Glu) c.1149T>A (p.Asp383Glu) | |
X | g.41474602T>C | CA516366066 | NYX | c.1134T>C (p.Asp378=) c.1149T>C (p.Asp383=) | gnomAD v4 |
X | g.41474602T>G | CA412992819 | NYX | c.1134T>G (p.Asp378Glu) c.1149T>G (p.Asp383Glu) | |
X | g.41474603G>A | CA412992822 | NYX | c.1135G>A (p.Gly379Ser) c.1150G>A (p.Gly384Ser) | dbSNP gnomAD v2 gnomAD v4 |
X | g.41474603G>C | CA412992824 | NYX | c.1135G>C (p.Gly379Arg) c.1150G>C (p.Gly384Arg) | |
X | g.41474603G= | CA2425928137 | NYX | c.1135G= (p.Gly379=) c.1150G= (p.Gly384=) | |
X | g.41474603G>T | CA412992826 | NYX | c.1135G>T (p.Gly379Cys) c.1150G>T (p.Gly384Cys) | |
X | g.41474604G>A | CA412992832 | NYX | c.1136G>A (p.Gly379Asp) c.1151G>A (p.Gly384Asp) | |
X | g.41474604G>C | CA412992830 | NYX | c.1136G>C (p.Gly379Ala) c.1151G>C (p.Gly384Ala) | |
X | g.41474604G>T | CA412992828 | NYX | c.1136G>T (p.Gly379Val) c.1151G>T (p.Gly384Val) | gnomAD v4 |
X | g.41474605C>A | CA516366071 | NYX | c.1137C>A (p.Gly379=) c.1152C>A (p.Gly384=) | |
X | g.41474605C= | CA2425928138 | NYX | c.1137C= (p.Gly379=) c.1152C= (p.Gly384=) | |
X | g.41474605C>G | CA516366072 | NYX | c.1137C>G (p.Gly379=) c.1152C>G (p.Gly384=) | |
X | g.41474605C>T | CA10389913 | NYX | c.1137C>T (p.Gly379=) c.1152C>T (p.Gly384=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474606C>A | CA412992835 | NYX | c.1138C>A (p.Leu380Ile) c.1153C>A (p.Leu385Ile) | |
X | g.41474606C>G | CA412992837 | NYX | c.1138C>G (p.Leu380Val) c.1153C>G (p.Leu385Val) | gnomAD v4 |
X | g.41474606C>T | CA412992839 | NYX | c.1138C>T (p.Leu380Phe) c.1153C>T (p.Leu385Phe) | |
X | g.41474607T>A | CA10389914 | NYX | c.1139T>A (p.Leu380His) c.1154T>A (p.Leu385His) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474607T>C | CA412992842 | NYX | c.1139T>C (p.Leu380Pro) c.1154T>C (p.Leu385Pro) | |
X | g.41474607T>G | CA412992844 | NYX | c.1139T>G (p.Leu380Arg) c.1154T>G (p.Leu385Arg) | |
X | g.41474607T= | CA2425928139 | NYX | c.1139T= (p.Leu380=) c.1154T= (p.Leu385=) |