Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.41474575_41474910del | CA2573050969 | NYX | c.1107_*11del (n.[c.1107_*11del;Ser369ArgfsTer10]) c.1122_*11del (n.[c.1122_*11del;Ser374ArgfsTer10]) | |
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=) | |
X | g.41474608C>A | CA516366077 | NYX | c.1140C>A (p.Leu380=) c.1155C>A (p.Leu385=) | |
X | g.41474608C>G | CA516366080 | NYX | c.1140C>G (p.Leu380=) c.1155C>G (p.Leu385=) | |
X | g.41474608C>T | CA516366079 | NYX | c.1140C>T (p.Leu380=) c.1155C>T (p.Leu385=) | |
X | g.41474609T>A | CA412992850 | NYX | c.1141T>A (p.Cys381Ser) c.1156T>A (p.Cys386Ser) | |
X | g.41474609T>C | CA412992847 | NYX | c.1141T>C (p.Cys381Arg) c.1156T>C (p.Cys386Arg) | |
X | g.41474609T>G | CA412992849 | NYX | c.1141T>G (p.Cys381Gly) c.1156T>G (p.Cys386Gly) | |
X | g.41474613_41474614del | CA2579588842 | NYX | c.1145_1146del (p.Val382GlyfsTer?) c.1160_1161del (p.Val387GlyfsTer?) | |
X | g.41474610G>A | CA412992852 | NYX | c.1142G>A (p.Cys381Tyr) c.1157G>A (p.Cys386Tyr) | gnomAD v4 |
X | g.41474610G>C | CA412992854 | NYX | c.1142G>C (p.Cys381Ser) c.1157G>C (p.Cys386Ser) | |
X | g.41474610G>T | CA412992856 | NYX | c.1142G>T (p.Cys381Phe) c.1157G>T (p.Cys386Phe) | |
X | g.41474611T>A | CA412992858 | NYX | c.1143T>A (p.Cys381Ter) c.1158T>A (p.Cys386Ter) | |
X | g.41474611T>C | CA516366081 | NYX | c.1143T>C (p.Cys381=) c.1158T>C (p.Cys386=) | |
X | g.41474611T>G | CA412992860 | NYX | c.1143T>G (p.Cys381Trp) c.1158T>G (p.Cys386Trp) | |
X | g.41474612G>A | CA412992862 | NYX | c.1144G>A (p.Val382Met) c.1159G>A (p.Val387Met) | dbSNP gnomAD v4 |
X | g.41474612G>C | CA412992865 | NYX | c.1144G>C (p.Val382Leu) c.1159G>C (p.Val387Leu) | |
X | g.41474612G= | CA2425928140 | NYX | c.1144G= (p.Val382=) c.1159G= (p.Val387=) | |
X | g.41474612G>T | CA412992864 | NYX | c.1144G>T (p.Val382Leu) c.1159G>T (p.Val387Leu) | gnomAD v4 |
X | g.41474613T>A | CA412992867 | NYX | c.1145T>A (p.Val382Glu) c.1160T>A (p.Val387Glu) | |
X | g.41474613T>C | CA412992868 | NYX | c.1145T>C (p.Val382Ala) c.1160T>C (p.Val387Ala) | |
X | g.41474613T>G | CA412992869 | NYX | c.1145T>G (p.Val382Gly) c.1160T>G (p.Val387Gly) | |
X | g.41474614G>A | CA516366084 | NYX | c.1146G>A (p.Val382=) c.1161G>A (p.Val387=) | gnomAD v4 |
X | g.41474614G>C | CA516366085 | NYX | c.1146G>C (p.Val382=) c.1161G>C (p.Val387=) | |
X | g.41474614G>T | CA516366086 | NYX | c.1146G>T (p.Val382=) c.1161G>T (p.Val387=) | gnomAD v4 |
X | g.41474615G>A | CA329217081 | NYX | c.1147G>A (p.Asp383Asn) c.1162G>A (p.Asp388Asn) | dbSNP gnomAD v4 COSMIC |
X | g.41474615G>C | CA412992873 | NYX | c.1147G>C (p.Asp383His) c.1162G>C (p.Asp388His) | gnomAD v4 |
X | g.41474615G= | CA2425928141 | NYX | c.1147G= (p.Asp383=) c.1162G= (p.Asp388=) | |
X | g.41474615G>T | CA412992874 | NYX | c.1147G>T (p.Asp383Tyr) c.1162G>T (p.Asp388Tyr) | |
X | g.41474616A>C | CA412992877 | NYX | c.1148A>C (p.Asp383Ala) c.1163A>C (p.Asp388Ala) | |
X | g.41474616A>G | CA412992879 | NYX | c.1148A>G (p.Asp383Gly) c.1163A>G (p.Asp388Gly) | |
X | g.41474616A>T | CA412992881 | NYX | c.1148A>T (p.Asp383Val) c.1163A>T (p.Asp388Val) | |
X | g.41474617C>A | CA412992883 | NYX | c.1149C>A (p.Asp383Glu) c.1164C>A (p.Asp388Glu) | |
X | g.41474617C= | CA2425928142 | NYX | c.1149C= (p.Asp383=) c.1164C= (p.Asp388=) | |
X | g.41474617C>G | CA412992884 | NYX | c.1149C>G (p.Asp383Glu) c.1164C>G (p.Asp388Glu) | gnomAD v4 |
X | g.41474617C>T | CA516366089 | NYX | c.1149C>T (p.Asp383=) c.1164C>T (p.Asp388=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474618C>A | CA412992888 | NYX | c.1150C>A (p.Pro384Thr) c.1165C>A (p.Pro389Thr) | gnomAD v4 |
X | g.41474618C= | CA2425928143 | NYX | c.1150C= (p.Pro384=) c.1165C= (p.Pro389=) | |
X | g.41474618C>G | CA412992890 | NYX | c.1150C>G (p.Pro384Ala) c.1165C>G (p.Pro389Ala) | |
X | g.41474618C>T | CA412992887 | NYX | c.1150C>T (p.Pro384Ser) c.1165C>T (p.Pro389Ser) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
X | g.41474619C>A | CA412992892 | NYX | c.1151C>A (p.Pro384His) c.1166C>A (p.Pro389His) | gnomAD v4 |
X | g.41474619C>G | CA412992896 | NYX | c.1151C>G (p.Pro384Arg) c.1166C>G (p.Pro389Arg) | |
X | g.41474619C>T | CA412992894 | NYX | c.1151C>T (p.Pro384Leu) c.1166C>T (p.Pro389Leu) | |
X | g.41474620C>A | CA516366097 | NYX | c.1152C>A (p.Pro384=) c.1167C>A (p.Pro389=) | |
X | g.41474620C= | CA2425928144 | NYX | c.1152C= (p.Pro384=) c.1167C= (p.Pro389=) | |
X | g.41474620C>G | CA516366098 | NYX | c.1152C>G (p.Pro384=) c.1167C>G (p.Pro389=) | |
X | g.41474620C>T | CA516366100 | NYX | c.1152C>T (p.Pro384=) c.1167C>T (p.Pro389=) | dbSNP gnomAD v2 gnomAD v4 |
X | g.41474621G>A | CA412992898 | NYX | c.1153G>A (p.Glu385Lys) c.1168G>A (p.Glu390Lys) | dbSNP |
X | g.41474621G>C | CA412992900 | NYX | c.1153G>C (p.Glu385Gln) c.1168G>C (p.Glu390Gln) | |
X | g.41474621G= | CA2425928145 | NYX | c.1153G= (p.Glu385=) c.1168G= (p.Glu390=) | |
X | g.41474621G>T | CA329217082 | NYX | c.1153G>T (p.Glu385Ter) c.1168G>T (p.Glu390Ter) | dbSNP gnomAD v4 COSMIC |
X | g.41474622A>C | CA412992903 | NYX | c.1154A>C (p.Glu385Ala) c.1169A>C (p.Glu390Ala) | |
X | g.41474622A>G | CA412992904 | NYX | c.1154A>G (p.Glu385Gly) c.1169A>G (p.Glu390Gly) | |
X | g.41474622A>T | CA412992906 | NYX | c.1154A>T (p.Glu385Val) c.1169A>T (p.Glu390Val) | |
X | g.41474623G>A | CA516366106 | NYX | c.1155G>A (p.Glu385=) c.1170G>A (p.Glu390=) | |
X | g.41474623G>C | CA329217083 | NYX | c.1155G>C (p.Glu385Asp) c.1170G>C (p.Glu390Asp) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474623G= | CA2425928146 | NYX | c.1155G= (p.Glu385=) c.1170G= (p.Glu390=) | |
X | g.41474623G>T | CA412992909 | NYX | c.1155G>T (p.Glu385Asp) c.1170G>T (p.Glu390Asp) | gnomAD v4 |
X | g.41474624G>A | CA412992911 | NYX | c.1156G>A (p.Glu386Lys) c.1171G>A (p.Glu391Lys) | |
X | g.41474624G>C | CA412992913 | NYX | c.1156G>C (p.Glu386Gln) c.1171G>C (p.Glu391Gln) | |
X | g.41474624G>T | CA412992915 | NYX | c.1156G>T (p.Glu386Ter) c.1171G>T (p.Glu391Ter) | |
X | g.41474625A>C | CA412992917 | NYX | c.1157A>C (p.Glu386Ala) c.1172A>C (p.Glu391Ala) | |
X | g.41474625A>G | CA412992918 | NYX | c.1157A>G (p.Glu386Gly) c.1172A>G (p.Glu391Gly) | |
X | g.41474625A>T | CA412992920 | NYX | c.1157A>T (p.Glu386Val) c.1172A>T (p.Glu391Val) | |
X | g.41474626G>A | CA516366112 | NYX | c.1158G>A (p.Glu386=) c.1173G>A (p.Glu391=) | gnomAD v4 |
X | g.41474626G>C | CA412992923 | NYX | c.1158G>C (p.Glu386Asp) c.1173G>C (p.Glu391Asp) | |
X | g.41474626G>T | CA412992922 | NYX | c.1158G>T (p.Glu386Asp) c.1173G>T (p.Glu391Asp) | gnomAD v4 |
X | g.41474627C>A | CA412992926 | NYX | c.1159C>A (p.Leu387Met) c.1174C>A (p.Leu392Met) | gnomAD v4 |
X | g.41474627C= | CA2425928147 | NYX | c.1159C= (p.Leu387=) c.1174C= (p.Leu392=) | |
X | g.41474627C>G | CA412992928 | NYX | c.1159C>G (p.Leu387Val) c.1174C>G (p.Leu392Val) | gnomAD v4 |
X | g.41474627C>T | CA329217084 | NYX | c.1159C>T (p.Leu387=) c.1174C>T (p.Leu392=) | ClinVar dbSNP gnomAD v4 |
X | g.41474628T>A | CA412992930 | NYX | c.1160T>A (p.Leu387Gln) c.1175T>A (p.Leu392Gln) | |
X | g.41474628T>C | CA412992932 | NYX | c.1160T>C (p.Leu387Pro) c.1175T>C (p.Leu392Pro) | gnomAD v4 |
X | g.41474628T>G | CA412992933 | NYX | c.1160T>G (p.Leu387Arg) c.1175T>G (p.Leu392Arg) | |
X | g.41474629G>A | CA516366117 | NYX | c.1161G>A (p.Leu387=) c.1176G>A (p.Leu392=) | |
X | g.41474629G>C | CA516366118 | NYX | c.1161G>C (p.Leu387=) c.1176G>C (p.Leu392=) | dbSNP gnomAD v3 gnomAD v4 |
X | g.41474629G= | CA2425928148 | NYX | c.1161G= (p.Leu387=) c.1176G= (p.Leu392=) | |
X | g.41474629G>T | CA516366120 | NYX | c.1161G>T (p.Leu387=) c.1176G>T (p.Leu392=) | gnomAD v4 |
X | g.41474630A>C | CA412992936 | NYX | c.1162A>C (p.Asn388His) c.1177A>C (p.Asn393His) | |
X | g.41474630A>G | CA412992938 | NYX | c.1162A>G (p.Asn388Asp) c.1177A>G (p.Asn393Asp) | |
X | g.41474630A>T | CA412992939 | NYX | c.1162A>T (p.Asn388Tyr) c.1177A>T (p.Asn393Tyr) | |
X | g.41474631A>C | CA412992942 | NYX | c.1163A>C (p.Asn388Thr) c.1178A>C (p.Asn393Thr) | |
X | g.41474631A>G | CA412992944 | NYX | c.1163A>G (p.Asn388Ser) c.1178A>G (p.Asn393Ser) | |
X | g.41474631A>T | CA412992945 | NYX | c.1163A>T (p.Asn388Ile) c.1178A>T (p.Asn393Ile) | |
X | g.41474632C>A | CA412992949 | NYX | c.1164C>A (p.Asn388Lys) c.1179C>A (p.Asn393Lys) | |
X | g.41474632C= | CA2425928149 | NYX | c.1164C= (p.Asn388=) c.1179C= (p.Asn393=) | |
X | g.41474632C>G | CA412992948 | NYX | c.1164C>G (p.Asn388Lys) c.1179C>G (p.Asn393Lys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
X | g.41474632C>T | CA516366128 | NYX | c.1164C>T (p.Asn388=) c.1179C>T (p.Asn393=) | |
X | g.41474633C>A | CA412992952 | NYX | c.1165C>A (p.Leu389Ile) c.1180C>A (p.Leu394Ile) | COSMIC |
X | g.41474633C= | CA2425928150 | NYX | c.1165C= (p.Leu389=) c.1180C= (p.Leu394=) | |
X | g.41474633C>G | CA412992954 | NYX | c.1165C>G (p.Leu389Val) c.1180C>G (p.Leu394Val) | |
X | g.41474633C>T | CA10389915 | NYX | c.1165C>T (p.Leu389Phe) c.1180C>T (p.Leu394Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474634T>A | CA412992957 | NYX | c.1166T>A (p.Leu389His) c.1181T>A (p.Leu394His) | |
X | g.41474634T>C | CA412992959 | NYX | c.1166T>C (p.Leu389Pro) c.1181T>C (p.Leu394Pro) | |
X | g.41474634T>G | CA412992960 | NYX | c.1166T>G (p.Leu389Arg) c.1181T>G (p.Leu394Arg) | |
X | g.41474635C>A | CA516366131 | NYX | c.1167C>A (p.Leu389=) c.1182C>A (p.Leu394=) | gnomAD v4 |
X | g.41474635C= | CA2425928151 | NYX | c.1167C= (p.Leu389=) c.1182C= (p.Leu394=) | |
X | g.41474635C>G | CA516366133 | NYX | c.1167C>G (p.Leu389=) c.1182C>G (p.Leu394=) | |
X | g.41474635C>T | CA10389916 | NYX | c.1167C>T (p.Leu389=) c.1182C>T (p.Leu394=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.41474636A>C | CA412992964 | NYX | c.1168A>C (p.Thr390Pro) c.1183A>C (p.Thr395Pro) | |
X | g.41474636A>G | CA412992966 | NYX | c.1168A>G (p.Thr390Ala) c.1183A>G (p.Thr395Ala) | |
X | g.41474636A>T | CA412992967 | NYX | c.1168A>T (p.Thr390Ser) c.1183A>T (p.Thr395Ser) | gnomAD v4 |
X | g.41474637C>A | CA412992970 | NYX | c.1169C>A (p.Thr390Asn) c.1184C>A (p.Thr395Asn) | gnomAD v4 |
X | g.41474637C= | CA2425928152 | NYX | c.1169C= (p.Thr390=) c.1184C= (p.Thr395=) | |
X | g.41474637C>G | CA412992972 | NYX | c.1169C>G (p.Thr390Ser) c.1184C>G (p.Thr395Ser) | |
X | g.41474637C>T | CA412992973 | NYX | c.1169C>T (p.Thr390Ile) c.1184C>T (p.Thr395Ile) | dbSNP gnomAD v2 gnomAD v4 |
X | g.41474638C>A | CA516366143 | NYX | c.1170C>A (p.Thr390=) c.1185C>A (p.Thr395=) | gnomAD v4 |
X | g.41474638C>G | CA516366140 | NYX | c.1170C>G (p.Thr390=) c.1185C>G (p.Thr395=) | |
X | g.41474638C>T | CA516366141 | NYX | c.1170C>T (p.Thr390=) c.1185C>T (p.Thr395=) | |
X | g.41474639A= | CA2425928153 | NYX | c.1171A= (p.Thr391=) c.1186A= (p.Thr396=) | |
X | g.41474639A>C | CA412992977 | NYX | c.1171A>C (p.Thr391Pro) c.1186A>C (p.Thr396Pro) | |
X | g.41474639A>G | CA412992975 | NYX | c.1171A>G (p.Thr391Ala) c.1186A>G (p.Thr396Ala) | dbSNP gnomAD v3 gnomAD v4 |
X | g.41474639A>T | CA10389917 | NYX | c.1171A>T (p.Thr391Ser) c.1186A>T (p.Thr396Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.41474640C>A | CA412992980 | NYX | c.1172C>A (p.Thr391Lys) c.1187C>A (p.Thr396Lys) | gnomAD v4 |
X | g.41474640C>G | CA412992981 | NYX | c.1172C>G (p.Thr391Arg) c.1187C>G (p.Thr396Arg) | gnomAD v4 |
X | g.41474640C>T | CA412992983 | NYX | c.1172C>T (p.Thr391Met) c.1187C>T (p.Thr396Met) | gnomAD v4 |
X | g.41474641G>A | CA516366147 | NYX | c.1173G>A (p.Thr391=) c.1188G>A (p.Thr396=) | dbSNP gnomAD v4 |
X | g.41474641G>C | CA516366148 | NYX | c.1173G>C (p.Thr391=) c.1188G>C (p.Thr396=) | |
X | g.41474641G= | CA2425928154 | NYX | c.1173G= (p.Thr391=) c.1188G= (p.Thr396=) | |
X | g.41474641G>T | CA516366150 | NYX | c.1173G>T (p.Thr391=) c.1188G>T (p.Thr396=) | |
X | g.41474642T>A | CA412992985 | NYX | c.1174T>A (p.Ser392Thr) c.1189T>A (p.Ser397Thr) | |
X | g.41474642T>C | CA412992987 | NYX | c.1174T>C (p.Ser392Pro) c.1189T>C (p.Ser397Pro) | |
X | g.41474642T>G | CA412992989 | NYX | c.1174T>G (p.Ser392Ala) c.1189T>G (p.Ser397Ala) | |
X | g.41474643C>A | CA412992991 | NYX | c.1175C>A (p.Ser392Tyr) c.1190C>A (p.Ser397Tyr) | ClinVar |
X | g.41474643C= | CA2425928155 | NYX | c.1175C= (p.Ser392=) c.1190C= (p.Ser397=) | |
X | g.41474643C>G | CA412992992 | NYX | c.1175C>G (p.Ser392Cys) c.1190C>G (p.Ser397Cys) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
X | g.41474643C>T | CA412992994 | NYX | c.1175C>T (p.Ser392Phe) c.1190C>T (p.Ser397Phe) | dbSNP gnomAD v4 |
X | g.41474644C>A | CA516366153 | NYX | c.1176C>A (p.Ser392=) c.1191C>A (p.Ser397=) | gnomAD v4 |
X | g.41474644C>G | CA516366155 | NYX | c.1176C>G (p.Ser392=) c.1191C>G (p.Ser397=) | gnomAD v4 |
X | g.41474644C>T | CA516366157 | NYX | c.1176C>T (p.Ser392=) c.1191C>T (p.Ser397=) | gnomAD v4 COSMIC |
X | g.41474645A>C | CA412992996 | NYX | c.1177A>C (p.Ser393Arg) c.1192A>C (p.Ser398Arg) | |
X | g.41474645A>G | CA412992997 | NYX | c.1177A>G (p.Ser393Gly) c.1192A>G (p.Ser398Gly) | |
X | g.41474645A>T | CA412992999 | NYX | c.1177A>T (p.Ser393Cys) c.1192A>T (p.Ser398Cys) | |
X | g.41474646G>A | CA412993003 | NYX | c.1178G>A (p.Ser393Asn) c.1193G>A (p.Ser398Asn) | ClinVar gnomAD v4 |
X | g.41474646G>C | CA412993005 | NYX | c.1178G>C (p.Ser393Thr) c.1193G>C (p.Ser398Thr) | |
X | g.41474646G>T | CA412993001 | NYX | c.1178G>T (p.Ser393Ile) c.1193G>T (p.Ser398Ile) | |
X | g.41474647T>A | CA412993007 | NYX | c.1179T>A (p.Ser393Arg) c.1194T>A (p.Ser398Arg) | gnomAD v4 |
X | g.41474647T>C | CA516366162 | NYX | c.1179T>C (p.Ser393=) c.1194T>C (p.Ser398=) | gnomAD v4 |
X | g.41474647T>G | CA412993008 | NYX | c.1179T>G (p.Ser393Arg) c.1194T>G (p.Ser398Arg) | |
X | g.41474648C>A | CA412993011 | NYX | c.1180C>A (p.Pro394Thr) c.1195C>A (p.Pro399Thr) | gnomAD v4 |
X | g.41474648C= | CA2425928156 | NYX | c.1180C= (p.Pro394=) c.1195C= (p.Pro399=) | |
X | g.41474648C>G | CA412993012 | NYX | c.1180C>G (p.Pro394Ala) c.1195C>G (p.Pro399Ala) | |
X | g.41474648C>T | CA412993014 | NYX | c.1180C>T (p.Pro394Ser) c.1195C>T (p.Pro399Ser) | dbSNP gnomAD v2 gnomAD v4 |
X | g.41474649C>A | CA412993020 | NYX | c.1181C>A (p.Pro394Gln) c.1196C>A (p.Pro399Gln) | |
X | g.41474649C= | CA2425928157 | NYX | c.1181C= (p.Pro394=) c.1196C= (p.Pro399=) | |
X | g.41474649C>G | CA412993018 | NYX | c.1181C>G (p.Pro394Arg) c.1196C>G (p.Pro399Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474649C>T | CA412993016 | NYX | c.1181C>T (p.Pro394Leu) c.1196C>T (p.Pro399Leu) | gnomAD v4 |
X | g.41474650A>C | CA516366169 | NYX | c.1182A>C (p.Pro394=) c.1197A>C (p.Pro399=) | |
X | g.41474650A>G | CA516366170 | NYX | c.1182A>G (p.Pro394=) c.1197A>G (p.Pro399=) | gnomAD v4 |
X | g.41474650A>T | CA516366172 | NYX | c.1182A>T (p.Pro394=) c.1197A>T (p.Pro399=) | |
X | g.41474651G>A | CA10389918 | NYX | c.1183G>A (p.Gly395Ser) c.1198G>A (p.Gly400Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474651G>C | CA412993022 | NYX | c.1183G>C (p.Gly395Arg) c.1198G>C (p.Gly400Arg) | |
X | g.41474651G= | CA2425928158 | NYX | c.1183G= (p.Gly395=) c.1198G= (p.Gly400=) | |
X | g.41474651G>T | CA412993024 | NYX | c.1183G>T (p.Gly395Cys) c.1198G>T (p.Gly400Cys) | gnomAD v4 |
X | g.41474652G>A | CA412993026 | NYX | c.1184G>A (p.Gly395Asp) c.1199G>A (p.Gly400Asp) | dbSNP gnomAD v2 |
X | g.41474652G>C | CA412993028 | NYX | c.1184G>C (p.Gly395Ala) c.1199G>C (p.Gly400Ala) | |
X | g.41474652G= | CA2425928159 | NYX | c.1184G= (p.Gly395=) c.1199G= (p.Gly400=) | |
X | g.41474652G>T | CA412993029 | NYX | c.1184G>T (p.Gly395Val) c.1199G>T (p.Gly400Val) | gnomAD v4 |
X | g.41474653C>A | CA516366176 | NYX | c.1185C>A (p.Gly395=) c.1200C>A (p.Gly400=) | gnomAD v4 |
X | g.41474653C>G | CA516366178 | NYX | c.1185C>G (p.Gly395=) c.1200C>G (p.Gly400=) | |
X | g.41474653C>T | CA516366180 | NYX | c.1185C>T (p.Gly395=) c.1200C>T (p.Gly400=) | gnomAD v4 |
X | g.41474654C>A | CA412993034 | NYX | c.1186C>A (p.Pro396Thr) c.1201C>A (p.Pro401Thr) | |
X | g.41474654C= | CA2425928160 | NYX | c.1186C= (p.Pro396=) c.1201C= (p.Pro401=) | |
X | g.41474654C>G | CA10389919 | NYX | c.1186C>G (p.Pro396Ala) c.1201C>G (p.Pro401Ala) | dbSNP ExAC |
X | g.41474654C>T | CA412993032 | NYX | c.1186C>T (p.Pro396Ser) c.1201C>T (p.Pro401Ser) | |
X | g.41474655C>A | CA412993036 | NYX | c.1187C>A (p.Pro396Gln) c.1202C>A (p.Pro401Gln) | gnomAD v4 |
X | g.41474655C= | CA2425928161 | NYX | c.1187C= (p.Pro396=) c.1202C= (p.Pro401=) | |
X | g.41474655C>G | CA10389920 | NYX | c.1187C>G (p.Pro396Arg) c.1202C>G (p.Pro401Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474655C>T | CA412993038 | NYX | c.1187C>T (p.Pro396Leu) c.1202C>T (p.Pro401Leu) | |
X | g.41474656G>A | CA223725 | NYX | c.1188G>A (p.Pro396=) c.1203G>A (p.Pro401=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474656G>C | CA516366186 | NYX | c.1188G>C (p.Pro396=) c.1203G>C (p.Pro401=) | |
X | g.41474656G= | CA2425928162 | NYX | c.1188G= (p.Pro396=) c.1203G= (p.Pro401=) | |
X | g.41474656G>T | CA516366187 | NYX | c.1188G>T (p.Pro396=) c.1203G>T (p.Pro401=) | gnomAD v4 |
X | g.41474657T>A | CA412993042 | NYX | c.1189T>A (p.Ser397Thr) c.1204T>A (p.Ser402Thr) | |
X | g.41474657T>C | CA412993043 | NYX | c.1189T>C (p.Ser397Pro) c.1204T>C (p.Ser402Pro) | |
X | g.41474657T>G | CA412993045 | NYX | c.1189T>G (p.Ser397Ala) c.1204T>G (p.Ser402Ala) | |
X | g.41474658C>A | CA412993048 | NYX | c.1190C>A (p.Ser397Tyr) c.1205C>A (p.Ser402Tyr) | gnomAD v4 |
X | g.41474658C= | CA2425928163 | NYX | c.1190C= (p.Ser397=) c.1205C= (p.Ser402=) | |
X | g.41474658C>G | CA412993050 | NYX | c.1190C>G (p.Ser397Cys) c.1205C>G (p.Ser402Cys) | |
X | g.41474658C>T | CA412993051 | NYX | c.1190C>T (p.Ser397Phe) c.1205C>T (p.Ser402Phe) | dbSNP gnomAD v2 |
X | g.41474661del | CA2693491328 | NYX | c.1193del (p.Pro398GlnfsTer8) c.1208del (p.Pro403GlnfsTer8) | gnomAD v4 |
X | g.41474658_41474659insT | CA2695233447 | NYX | c.1190_1191insT (p.Glu399ArgfsTer?) c.1205_1206insT (p.Glu404ArgfsTer?) | |
X | g.41474659C>A | CA516366193 | NYX | c.1191C>A (p.Ser397=) c.1206C>A (p.Ser402=) | gnomAD v4 |
X | g.41474659C>G | CA516366194 | NYX | c.1191C>G (p.Ser397=) c.1206C>G (p.Ser402=) | |
X | g.41474659C>T | CA516366195 | NYX | c.1191C>T (p.Ser397=) c.1206C>T (p.Ser402=) | |
X | g.41474660C>A | CA412993053 | NYX | c.1192C>A (p.Pro398Thr) c.1207C>A (p.Pro403Thr) | |
X | g.41474660C>G | CA412993054 | NYX | c.1192C>G (p.Pro398Ala) c.1207C>G (p.Pro403Ala) | |
X | g.41474660C>T | CA412993056 | NYX | c.1192C>T (p.Pro398Ser) c.1207C>T (p.Pro403Ser) | |
X | g.41474661C>A | CA412993059 | NYX | c.1193C>A (p.Pro398Gln) c.1208C>A (p.Pro403Gln) | |
X | g.41474661C= | CA2425928164 | NYX | c.1193C= (p.Pro398=) c.1208C= (p.Pro403=) | |
X | g.41474661C>G | CA412993062 | NYX | c.1193C>G (p.Pro398Arg) c.1208C>G (p.Pro403Arg) | |
X | g.41474661C>T | CA412993060 | NYX | c.1193C>T (p.Pro398Leu) c.1208C>T (p.Pro403Leu) | dbSNP gnomAD v3 gnomAD v4 |
X | g.41474662A>C | CA516366200 | NYX | c.1194A>C (p.Pro398=) c.1209A>C (p.Pro403=) | |
X | g.41474662A>G | CA516366202 | NYX | c.1194A>G (p.Pro398=) c.1209A>G (p.Pro403=) | |
X | g.41474662A>T | CA516366203 | NYX | c.1194A>T (p.Pro398=) c.1209A>T (p.Pro403=) | |
X | g.41474663G>A | CA412993065 | NYX | c.1195G>A (p.Glu399Lys) c.1210G>A (p.Glu404Lys) | |
X | g.41474663G>C | CA412993066 | NYX | c.1195G>C (p.Glu399Gln) c.1210G>C (p.Glu404Gln) | |
X | g.41474663G>T | CA412993068 | NYX | c.1195G>T (p.Glu399Ter) c.1210G>T (p.Glu404Ter) | |
X | g.41474664A>C | CA412993070 | NYX | c.1196A>C (p.Glu399Ala) c.1211A>C (p.Glu404Ala) | |
X | g.41474664A>G | CA412993072 | NYX | c.1196A>G (p.Glu399Gly) c.1211A>G (p.Glu404Gly) | |
X | g.41474664A>T | CA412993074 | NYX | c.1196A>T (p.Glu399Val) c.1211A>T (p.Glu404Val) | |
X | g.41474665A= | CA2425928165 | NYX | c.1197A= (p.Glu399=) c.1212A= (p.Glu404=) | |
X | g.41474665A>C | CA412993077 | NYX | c.1197A>C (p.Glu399Asp) c.1212A>C (p.Glu404Asp) | |
X | g.41474665A>G | CA516366218 | NYX | c.1197A>G (p.Glu399=) c.1212A>G (p.Glu404=) | dbSNP |
X | g.41474665A>T | CA412993076 | NYX | c.1197A>T (p.Glu399Asp) c.1212A>T (p.Glu404Asp) | |
X | g.41474666C>A | CA412993079 | NYX | c.1198C>A (p.Pro400Thr) c.1213C>A (p.Pro405Thr) | |
X | g.41474666C>G | CA412993081 | NYX | c.1198C>G (p.Pro400Ala) c.1213C>G (p.Pro405Ala) | |
X | g.41474666C>T | CA412993082 | NYX | c.1198C>T (p.Pro400Ser) c.1213C>T (p.Pro405Ser) | |
X | g.41474667C>A | CA412993085 | NYX | c.1199C>A (p.Pro400Gln) c.1214C>A (p.Pro405Gln) | gnomAD v4 |
X | g.41474667C= | CA2425928166 | NYX | c.1199C= (p.Pro400=) c.1214C= (p.Pro405=) | |
X | g.41474667C>G | CA412993086 | NYX | c.1199C>G (p.Pro400Arg) c.1214C>G (p.Pro405Arg) | dbSNP |
X | g.41474667C>T | CA412993088 | NYX | c.1199C>T (p.Pro400Leu) c.1214C>T (p.Pro405Leu) | |
X | g.41474668A>C | CA516366230 | NYX | c.1200A>C (p.Pro400=) c.1215A>C (p.Pro405=) | |
X | g.41474668A>G | CA516366228 | NYX | c.1200A>G (p.Pro400=) c.1215A>G (p.Pro405=) | gnomAD v4 |
X | g.41474668A>T | CA516366225 | NYX | c.1200A>T (p.Pro400=) c.1215A>T (p.Pro405=) | gnomAD v4 |
X | g.41474669G>A | CA412993090 | NYX | c.1201G>A (p.Ala401Thr) c.1216G>A (p.Ala406Thr) | |
X | g.41474669G>C | CA412993094 | NYX | c.1201G>C (p.Ala401Pro) c.1216G>C (p.Ala406Pro) | |
X | g.41474669G>T | CA412993092 | NYX | c.1201G>T (p.Ala401Ser) c.1216G>T (p.Ala406Ser) | |
X | g.41474670C>A | CA412993096 | NYX | c.1202C>A (p.Ala401Glu) c.1217C>A (p.Ala406Glu) | gnomAD v4 |
X | g.41474670C= | CA2425928167 | NYX | c.1202C= (p.Ala401=) c.1217C= (p.Ala406=) | |
X | g.41474670C>G | CA201701 | NYX | c.1202C>G (p.Ala401Gly) c.1217C>G (p.Ala406Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474670C>T | CA10389921 | NYX | c.1202C>T (p.Ala401Val) c.1217C>T (p.Ala406Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
X | g.41474671G>A | CA10389922 | NYX | c.1203G>A (p.Ala401=) c.1218G>A (p.Ala406=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474671G>C | CA516366261 | NYX | c.1203G>C (p.Ala401=) c.1218G>C (p.Ala406=) | |
X | g.41474671G= | CA2425928168 | NYX | c.1203G= (p.Ala401=) c.1218G= (p.Ala406=) | |
X | g.41474671G>T | CA516366257 | NYX | c.1203G>T (p.Ala401=) c.1218G>T (p.Ala406=) | gnomAD v4 |
X | g.41474672G>A | CA412993101 | NYX | c.1204G>A (p.Ala402Thr) c.1219G>A (p.Ala407Thr) | |
X | g.41474672G>C | CA412993103 | NYX | c.1204G>C (p.Ala402Pro) c.1219G>C (p.Ala407Pro) | |
X | g.41474672G>T | CA412993105 | NYX | c.1204G>T (p.Ala402Ser) c.1219G>T (p.Ala407Ser) | gnomAD v4 |
X | g.41474673C>A | CA412993106 | NYX | c.1205C>A (p.Ala402Asp) c.1220C>A (p.Ala407Asp) | gnomAD v4 |
X | g.41474673C= | CA2425928169 | NYX | c.1205C= (p.Ala402=) c.1220C= (p.Ala407=) | |
X | g.41474673C>G | CA412993108 | NYX | c.1205C>G (p.Ala402Gly) c.1220C>G (p.Ala407Gly) | |
X | g.41474673C>T | CA10389923 | NYX | c.1205C>T (p.Ala402Val) c.1220C>T (p.Ala407Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.41474674C>A | CA516366267 | NYX | c.1206C>A (p.Ala402=) c.1221C>A (p.Ala407=) | gnomAD v4 |
X | g.41474674C>G | CA516366269 | NYX | c.1206C>G (p.Ala402=) c.1221C>G (p.Ala407=) | |
X | g.41474674C>T | CA516366271 | NYX | c.1206C>T (p.Ala402=) c.1221C>T (p.Ala407=) | |
X | g.41474675A>C | CA412993114 | NYX | c.1207A>C (p.Thr403Pro) c.1222A>C (p.Thr408Pro) | |
X | g.41474675A>G | CA412993112 | NYX | c.1207A>G (p.Thr403Ala) c.1222A>G (p.Thr408Ala) | |
X | g.41474675A>T | CA412993110 | NYX | c.1207A>T (p.Thr403Ser) c.1222A>T (p.Thr408Ser) | |
X | g.41474676C>A | CA412993116 | NYX | c.1208C>A (p.Thr403Asn) c.1223C>A (p.Thr408Asn) | |
X | g.41474676C>G | CA412993120 | NYX | c.1208C>G (p.Thr403Ser) c.1223C>G (p.Thr408Ser) | |
X | g.41474676C>T | CA412993118 | NYX | c.1208C>T (p.Thr403Ile) c.1223C>T (p.Thr408Ile) |