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.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) | |
X | g.41474677C>A | CA516366285 | NYX | c.1209C>A (p.Thr403=) c.1224C>A (p.Thr408=) | gnomAD v4 |
X | g.41474677C>G | CA516366287 | NYX | c.1209C>G (p.Thr403=) c.1224C>G (p.Thr408=) | |
X | g.41474677C>T | CA516366292 | NYX | c.1209C>T (p.Thr403=) c.1224C>T (p.Thr408=) | |
X | g.41474678A>C | CA412993122 | NYX | c.1210A>C (p.Thr404Pro) c.1225A>C (p.Thr409Pro) | |
X | g.41474678A>G | CA412993125 | NYX | c.1210A>G (p.Thr404Ala) c.1225A>G (p.Thr409Ala) | |
X | g.41474678A>T | CA412993123 | NYX | c.1210A>T (p.Thr404Ser) c.1225A>T (p.Thr409Ser) | |
X | g.41474679C>A | CA412993128 | NYX | c.1211C>A (p.Thr404Asn) c.1226C>A (p.Thr409Asn) | |
X | g.41474679C= | CA2425928170 | NYX | c.1211C= (p.Thr404=) c.1226C= (p.Thr409=) | |
X | g.41474679C>G | CA412993130 | NYX | c.1211C>G (p.Thr404Ser) c.1226C>G (p.Thr409Ser) | |
X | g.41474679C>T | CA329217085 | NYX | c.1211C>T (p.Thr404Ile) c.1226C>T (p.Thr409Ile) | dbSNP gnomAD v4 |
X | g.41474680C>A | CA516366299 | NYX | c.1212C>A (p.Thr404=) c.1227C>A (p.Thr409=) | gnomAD v4 |
X | g.41474680C= | CA2425928171 | NYX | c.1212C= (p.Thr404=) c.1227C= (p.Thr409=) | |
X | g.41474680C>G | CA516366301 | NYX | c.1212C>G (p.Thr404=) c.1227C>G (p.Thr409=) | dbSNP gnomAD v3 gnomAD v4 |
X | g.41474680C>T | CA10389924 | NYX | c.1212C>T (p.Thr404=) c.1227C>T (p.Thr409=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474681G>A | CA412993135 | NYX | c.1213G>A (p.Val405Met) c.1228G>A (p.Val410Met) | ClinVar gnomAD v4 |
X | g.41474681G>C | CA412993133 | NYX | c.1213G>C (p.Val405Leu) c.1228G>C (p.Val410Leu) | |
X | g.41474681G>T | CA412993134 | NYX | c.1213G>T (p.Val405Leu) c.1228G>T (p.Val410Leu) | |
X | g.41474682T>A | CA412993137 | NYX | c.1214T>A (p.Val405Glu) c.1229T>A (p.Val410Glu) | |
X | g.41474682T>C | CA412993139 | NYX | c.1214T>C (p.Val405Ala) c.1229T>C (p.Val410Ala) | |
X | g.41474682T>G | CA412993140 | NYX | c.1214T>G (p.Val405Gly) c.1229T>G (p.Val410Gly) | |
X | g.41474683del | CA2820585903 | NYX | c.1215del (p.Ser406AlafsTer?) c.1230del (p.Ser411AlafsTer?) | |
X | g.41474683G>A | CA516366308 | NYX | c.1215G>A (p.Val405=) c.1230G>A (p.Val410=) | dbSNP gnomAD v2 |
X | g.41474683G>C | CA516366309 | NYX | c.1215G>C (p.Val405=) c.1230G>C (p.Val410=) | |
X | g.41474683G= | CA2425928172 | NYX | c.1215G= (p.Val405=) c.1230G= (p.Val410=) | |
X | g.41474683G>T | CA516366310 | NYX | c.1215G>T (p.Val405=) c.1230G>T (p.Val410=) | gnomAD v4 |
X | g.41474684A= | CA2425928173 | NYX | c.1216A= (p.Ser406=) c.1231A= (p.Ser411=) | |
X | g.41474684A>C | CA412993142 | NYX | c.1216A>C (p.Ser406Arg) c.1231A>C (p.Ser411Arg) | |
X | g.41474684A>G | CA10389925 | NYX | c.1216A>G (p.Ser406Gly) c.1231A>G (p.Ser411Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.41474684A>T | CA412993144 | NYX | c.1216A>T (p.Ser406Cys) c.1231A>T (p.Ser411Cys) | |
X | g.41474685G>A | CA412993147 | NYX | c.1217G>A (p.Ser406Asn) c.1232G>A (p.Ser411Asn) | |
X | g.41474685G>C | CA412993148 | NYX | c.1217G>C (p.Ser406Thr) c.1232G>C (p.Ser411Thr) | |
X | g.41474685G>T | CA412993150 | NYX | c.1217G>T (p.Ser406Ile) c.1232G>T (p.Ser411Ile) | gnomAD v4 |
X | g.41474686C>A | CA412993152 | NYX | c.1218C>A (p.Ser406Arg) c.1233C>A (p.Ser411Arg) | |
X | g.41474686C= | CA2425928174 | NYX | c.1218C= (p.Ser406=) c.1233C= (p.Ser411=) | |
X | g.41474686C>G | CA412993154 | NYX | c.1218C>G (p.Ser406Arg) c.1233C>G (p.Ser411Arg) | ClinVar dbSNP gnomAD v4 |
X | g.41474686C>T | CA516366333 | NYX | c.1218C>T (p.Ser406=) c.1233C>T (p.Ser411=) | gnomAD v4 |
X | g.41474687A>C | CA516366341 | NYX | c.1219A>C (p.Arg407=) c.1234A>C (p.Arg412=) | |
X | g.41474687A>G | CA412993155 | NYX | c.1219A>G (p.Arg407Gly) c.1234A>G (p.Arg412Gly) | |
X | g.41474687A>T | CA412993157 | NYX | c.1219A>T (p.Arg407Trp) c.1234A>T (p.Arg412Trp) | |
X | g.41474688G>A | CA412993159 | NYX | c.1220G>A (p.Arg407Lys) c.1235G>A (p.Arg412Lys) | ClinVar dbSNP |
X | g.41474688G>C | CA412993161 | NYX | c.1220G>C (p.Arg407Thr) c.1235G>C (p.Arg412Thr) | |
X | g.41474688G>T | CA412993163 | NYX | c.1220G>T (p.Arg407Met) c.1235G>T (p.Arg412Met) | gnomAD v4 |
X | g.41474689G>A | CA516366344 | NYX | c.1221G>A (p.Arg407=) c.1236G>A (p.Arg412=) | |
X | g.41474689G>C | CA412993164 | NYX | c.1221G>C (p.Arg407Ser) c.1236G>C (p.Arg412Ser) | |
X | g.41474689G>T | CA412993166 | NYX | c.1221G>T (p.Arg407Ser) c.1236G>T (p.Arg412Ser) | |
X | g.41474690T>A | CA412993168 | NYX | c.1222T>A (p.Phe408Ile) c.1237T>A (p.Phe413Ile) | |
X | g.41474690T>C | CA412993170 | NYX | c.1222T>C (p.Phe408Leu) c.1237T>C (p.Phe413Leu) | |
X | g.41474690T>G | CA412993171 | NYX | c.1222T>G (p.Phe408Val) c.1237T>G (p.Phe413Val) | |
X | g.41474691T>A | CA412993174 | NYX | c.1223T>A (p.Phe408Tyr) c.1238T>A (p.Phe413Tyr) | |
X | g.41474691T>C | CA412993175 | NYX | c.1223T>C (p.Phe408Ser) c.1238T>C (p.Phe413Ser) | |
X | g.41474691T>G | CA412993176 | NYX | c.1223T>G (p.Phe408Cys) c.1238T>G (p.Phe413Cys) | |
X | g.41474691_41474694delinsTCAG | CA2425928175 | NYX | c.1223_1226delinsTCAG (p.Phe408=) c.1238_1241delinsTCAG (p.Phe413=) | |
X | g.41474692C>A | CA412993182 | NYX | c.1224C>A (p.Phe408Leu) c.1239C>A (p.Phe413Leu) | gnomAD v4 |
X | g.41474692C>G | CA412993180 | NYX | c.1224C>G (p.Phe408Leu) c.1239C>G (p.Phe413Leu) | gnomAD v4 |
X | g.41474692C>T | CA516366355 | NYX | c.1224C>T (p.Phe408=) c.1239C>T (p.Phe413=) | gnomAD v4 |
X | g.41474696_41474698del | CA10389926 | NYX | c.1228_1230del (p.Ser410del) c.1243_1245del (p.Ser415del) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474693A>C | CA412993184 | NYX | c.1225A>C (p.Ser409Arg) c.1240A>C (p.Ser414Arg) | |
X | g.41474693A>G | CA412993185 | NYX | c.1225A>G (p.Ser409Gly) c.1240A>G (p.Ser414Gly) | gnomAD v4 |
X | g.41474693A>T | CA412993187 | NYX | c.1225A>T (p.Ser409Cys) c.1240A>T (p.Ser414Cys) | |
X | g.41474694G>A | CA412993190 | NYX | c.1226G>A (p.Ser409Asn) c.1241G>A (p.Ser414Asn) | gnomAD v4 |
X | g.41474694G>C | CA412993191 | NYX | c.1226G>C (p.Ser409Thr) c.1241G>C (p.Ser414Thr) | |
X | g.41474694G= | CA2425928176 | NYX | c.1226G= (p.Ser409=) c.1241G= (p.Ser414=) | |
X | g.41474694G>T | CA10389927 | NYX | c.1226G>T (p.Ser409Ile) c.1241G>T (p.Ser414Ile) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.41474695C>A | CA412993194 | NYX | c.1227C>A (p.Ser409Arg) c.1242C>A (p.Ser414Arg) | gnomAD v4 |
X | g.41474695C>G | CA412993196 | NYX | c.1227C>G (p.Ser409Arg) c.1242C>G (p.Ser414Arg) | |
X | g.41474695C>T | CA516366370 | NYX | c.1227C>T (p.Ser409=) c.1242C>T (p.Ser414=) | gnomAD v4 |
X | g.41474696A>C | CA412993198 | NYX | c.1228A>C (p.Ser410Arg) c.1243A>C (p.Ser415Arg) | |
X | g.41474696A>G | CA412993200 | NYX | c.1228A>G (p.Ser410Gly) c.1243A>G (p.Ser415Gly) | |
X | g.41474696A>T | CA412993202 | NYX | c.1228A>T (p.Ser410Cys) c.1243A>T (p.Ser415Cys) | |
X | g.41474697G>A | CA10389928 | NYX | c.1229G>A (p.Ser410Asn) c.1244G>A (p.Ser415Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474697G>C | CA412993207 | NYX | c.1229G>C (p.Ser410Thr) c.1244G>C (p.Ser415Thr) | |
X | g.41474697G= | CA2425928177 | NYX | c.1229G= (p.Ser410=) c.1244G= (p.Ser415=) | |
X | g.41474697G>T | CA412993204 | NYX | c.1229G>T (p.Ser410Ile) c.1244G>T (p.Ser415Ile) | gnomAD v4 |
X | g.41474698C>A | CA412993211 | NYX | c.1230C>A (p.Ser410Arg) c.1245C>A (p.Ser415Arg) | gnomAD v4 |
X | g.41474698C= | CA2425928178 | NYX | c.1230C= (p.Ser410=) c.1245C= (p.Ser415=) | |
X | g.41474698C>G | CA412993212 | NYX | c.1230C>G (p.Ser410Arg) c.1245C>G (p.Ser415Arg) | gnomAD v4 |
X | g.41474698C>T | CA10389929 | NYX | c.1230C>T (p.Ser410=) c.1245C>T (p.Ser415=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474699C>A | CA412993215 | NYX | c.1231C>A (p.Leu411Ile) c.1246C>A (p.Leu416Ile) | gnomAD v4 |
X | g.41474699C>G | CA412993217 | NYX | c.1231C>G (p.Leu411Val) c.1246C>G (p.Leu416Val) | |
X | g.41474699C>T | CA412993219 | NYX | c.1231C>T (p.Leu411Phe) c.1246C>T (p.Leu416Phe) | gnomAD v4 |
X | g.41474701_41474715del | CA2693491329 | NYX | c.1233_1247del (p.Leu412_Leu416del) c.1248_1262del (p.Leu417_Leu421del) | gnomAD v4 |
X | g.41474700T>A | CA412993222 | NYX | c.1232T>A (p.Leu411His) c.1247T>A (p.Leu416His) | |
X | g.41474700T>C | CA412993223 | NYX | c.1232T>C (p.Leu411Pro) c.1247T>C (p.Leu416Pro) | |
X | g.41474700T>G | CA412993224 | NYX | c.1232T>G (p.Leu411Arg) c.1247T>G (p.Leu416Arg) | |
X | g.41474701C>A | CA516366391 | NYX | c.1233C>A (p.Leu411=) c.1248C>A (p.Leu416=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474701C= | CA2425928179 | NYX | c.1233C= (p.Leu411=) c.1248C= (p.Leu416=) | |
X | g.41474701C>G | CA516366393 | NYX | c.1233C>G (p.Leu411=) c.1248C>G (p.Leu416=) | gnomAD v4 COSMIC |
X | g.41474701C>T | CA516366395 | NYX | c.1233C>T (p.Leu411=) c.1248C>T (p.Leu416=) | dbSNP gnomAD v4 |
X | g.41474702C>A | CA412993225 | NYX | c.1234C>A (p.Leu412Ile) c.1249C>A (p.Leu417Ile) | |
X | g.41474702C= | CA2425928180 | NYX | c.1234C= (p.Leu412=) c.1249C= (p.Leu417=) | |
X | g.41474702C>G | CA10389930 | NYX | c.1234C>G (p.Leu412Val) c.1249C>G (p.Leu417Val) | dbSNP ExAC gnomAD v2 |
X | g.41474702C>T | CA329217086 | NYX | c.1234C>T (p.Leu412Phe) c.1249C>T (p.Leu417Phe) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
X | g.41474703T>A | CA412993238 | NYX | c.1235T>A (p.Leu412His) c.1250T>A (p.Leu417His) | |
X | g.41474703T>C | CA412993234 | NYX | c.1235T>C (p.Leu412Pro) c.1250T>C (p.Leu417Pro) | gnomAD v4 |
X | g.41474703T>G | CA412993232 | NYX | c.1235T>G (p.Leu412Arg) c.1250T>G (p.Leu417Arg) | gnomAD v4 |
X | g.41474704C>A | CA516366417 | NYX | c.1236C>A (p.Leu412=) c.1251C>A (p.Leu417=) | gnomAD v4 |
X | g.41474704C= | CA2425928181 | NYX | c.1236C= (p.Leu412=) c.1251C= (p.Leu417=) | |
X | g.41474704C>G | CA516366421 | NYX | c.1236C>G (p.Leu412=) c.1251C>G (p.Leu417=) | |
X | g.41474704C>T | CA10389931 | NYX | c.1236C>T (p.Leu412=) c.1251C>T (p.Leu417=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474705T>A | CA412993246 | NYX | c.1237T>A (p.Ser413Thr) c.1252T>A (p.Ser418Thr) | gnomAD v4 |
X | g.41474705T>C | CA412993266 | NYX | c.1237T>C (p.Ser413Pro) c.1252T>C (p.Ser418Pro) | |
X | g.41474705T>G | CA412993269 | NYX | c.1237T>G (p.Ser413Ala) c.1252T>G (p.Ser418Ala) | |
X | g.41474706C>A | CA412993273 | NYX | c.1238C>A (p.Ser413Tyr) c.1253C>A (p.Ser418Tyr) | dbSNP |
X | g.41474706C= | CA2425928182 | NYX | c.1238C= (p.Ser413=) c.1253C= (p.Ser418=) | |
X | g.41474706C>G | CA10389932 | NYX | c.1238C>G (p.Ser413Cys) c.1253C>G (p.Ser418Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.41474706C>T | CA412993280 | NYX | c.1238C>T (p.Ser413Phe) c.1253C>T (p.Ser418Phe) | |
X | g.41474707C>A | CA516366431 | NYX | c.1239C>A (p.Ser413=) c.1254C>A (p.Ser418=) | |
X | g.41474707C>G | CA516366430 | NYX | c.1239C>G (p.Ser413=) c.1254C>G (p.Ser418=) | |
X | g.41474707C>T | CA516366429 | NYX | c.1239C>T (p.Ser413=) c.1254C>T (p.Ser418=) | |
X | g.41474708A= | CA2425928183 | NYX | c.1240A= (p.Lys414=) c.1255A= (p.Lys419=) | |
X | g.41474708A>C | CA412993283 | NYX | c.1240A>C (p.Lys414Gln) c.1255A>C (p.Lys419Gln) | |
X | g.41474708A>G | CA412993285 | NYX | c.1240A>G (p.Lys414Glu) c.1255A>G (p.Lys419Glu) | dbSNP gnomAD v2 gnomAD v4 |
X | g.41474708A>T | CA412993288 | NYX | c.1240A>T (p.Lys414Ter) c.1255A>T (p.Lys419Ter) | |
X | g.41474708_41474709insG | CA2820585906 | NYX | c.1240_1241insG (p.Lys414ArgfsTer?) c.1255_1256insG (p.Lys419ArgfsTer?) | |
X | g.41474709A>C | CA412993292 | NYX | c.1241A>C (p.Lys414Thr) c.1256A>C (p.Lys419Thr) | |
X | g.41474709A>G | CA412993294 | NYX | c.1241A>G (p.Lys414Arg) c.1256A>G (p.Lys419Arg) | |
X | g.41474709A>T | CA412993302 | NYX | c.1241A>T (p.Lys414Met) c.1256A>T (p.Lys419Met) | |
X | g.41474710G>A | CA516366445 | NYX | c.1242G>A (p.Lys414=) c.1257G>A (p.Lys419=) | gnomAD v4 |
X | g.41474710G>C | CA412993305 | NYX | c.1242G>C (p.Lys414Asn) c.1257G>C (p.Lys419Asn) | |
X | g.41474710G= | CA2425928184 | NYX | c.1242G= (p.Lys414=) c.1257G= (p.Lys419=) | |
X | g.41474710G>T | CA412993306 | NYX | c.1242G>T (p.Lys414Asn) c.1257G>T (p.Lys419Asn) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
X | g.41474711C>A | CA412993309 | NYX | c.1243C>A (p.Leu415Met) c.1258C>A (p.Leu420Met) | gnomAD v4 |
X | g.41474711C= | CA2425928185 | NYX | c.1243C= (p.Leu415=) c.1258C= (p.Leu420=) | |
X | g.41474711C>G | CA412993312 | NYX | c.1243C>G (p.Leu415Val) c.1258C>G (p.Leu420Val) | |
X | g.41474711C>T | CA516366450 | NYX | c.1243C>T (p.Leu415=) c.1258C>T (p.Leu420=) | dbSNP gnomAD v4 |
X | g.41474712T>A | CA412993315 | NYX | c.1244T>A (p.Leu415Gln) c.1259T>A (p.Leu420Gln) | |
X | g.41474712T>C | CA412993318 | NYX | c.1244T>C (p.Leu415Pro) c.1259T>C (p.Leu420Pro) | |
X | g.41474712T>G | CA412993321 | NYX | c.1244T>G (p.Leu415Arg) c.1259T>G (p.Leu420Arg) | |
X | g.41474713G>A | CA516366458 | NYX | c.1245G>A (p.Leu415=) c.1260G>A (p.Leu420=) | gnomAD v4 |
X | g.41474713G>C | CA516366460 | NYX | c.1245G>C (p.Leu415=) c.1260G>C (p.Leu420=) | |
X | g.41474713G= | CA2425928186 | NYX | c.1245G= (p.Leu415=) c.1260G= (p.Leu420=) | |
X | g.41474713G>T | CA516366459 | NYX | c.1245G>T (p.Leu415=) c.1260G>T (p.Leu420=) | ClinVar dbSNP gnomAD v4 |
X | g.41474714C>A | CA412993324 | NYX | c.1246C>A (p.Leu416Met) c.1261C>A (p.Leu421Met) | gnomAD v4 |
X | g.41474714C= | CA2425928187 | NYX | c.1246C= (p.Leu416=) c.1261C= (p.Leu421=) | |
X | g.41474714C>G | CA412993327 | NYX | c.1246C>G (p.Leu416Val) c.1261C>G (p.Leu421Val) | |
X | g.41474714C>T | CA516366469 | NYX | c.1246C>T (p.Leu416=) c.1261C>T (p.Leu421=) | dbSNP gnomAD v4 |
X | g.41474714_41474715dup | CA915951045 | NYX | c.1246_1247dup (p.Ala417TrpfsTer?) c.1261_1262dup (p.Ala422TrpfsTer?) | ClinVar dbSNP |
X | g.41474715T>A | CA412993331 | NYX | c.1247T>A (p.Leu416Gln) c.1262T>A (p.Leu421Gln) | COSMIC |
X | g.41474715T>C | CA412993334 | NYX | c.1247T>C (p.Leu416Pro) c.1262T>C (p.Leu421Pro) | |
X | g.41474715T>G | CA412993336 | NYX | c.1247T>G (p.Leu416Arg) c.1262T>G (p.Leu421Arg) | |
X | g.41474716G>A | CA10389933 | NYX | c.1248G>A (p.Leu416=) c.1263G>A (p.Leu421=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.41474716G>C | CA516366473 | NYX | c.1248G>C (p.Leu416=) c.1263G>C (p.Leu421=) | |
X | g.41474716G= | CA2425928188 | NYX | c.1248G= (p.Leu416=) c.1263G= (p.Leu421=) | |
X | g.41474716G>T | CA516366477 | NYX | c.1248G>T (p.Leu416=) c.1263G>T (p.Leu421=) | |
X | g.41474717G>A | CA412993339 | NYX | c.1249G>A (p.Ala417Thr) c.1264G>A (p.Ala422Thr) | gnomAD v4 |
X | g.41474717G>C | CA412993341 | NYX | c.1249G>C (p.Ala417Pro) c.1264G>C (p.Ala422Pro) | |
X | g.41474717G>T | CA412993343 | NYX | c.1249G>T (p.Ala417Ser) c.1264G>T (p.Ala422Ser) | |
X | g.41474718C>A | CA412993345 | NYX | c.1250C>A (p.Ala417Asp) c.1265C>A (p.Ala422Asp) | gnomAD v4 |
X | g.41474718C>G | CA412993348 | NYX | c.1250C>G (p.Ala417Gly) c.1265C>G (p.Ala422Gly) | |
X | g.41474718C>T | CA412993347 | NYX | c.1250C>T (p.Ala417Val) c.1265C>T (p.Ala422Val) | gnomAD v4 |
X | g.41474719C>A | CA516366489 | NYX | c.1251C>A (p.Ala417=) c.1266C>A (p.Ala422=) | |
X | g.41474719C= | CA2425928189 | NYX | c.1251C= (p.Ala417=) c.1266C= (p.Ala422=) | |
X | g.41474719C>G | CA516366490 | NYX | c.1251C>G (p.Ala417=) c.1266C>G (p.Ala422=) | gnomAD v4 |
X | g.41474719C>T | CA10389934 | NYX | c.1251C>T (p.Ala417=) c.1266C>T (p.Ala422=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.41474720C>A | CA412993351 | NYX | c.1252C>A (p.Pro418Thr) c.1267C>A (p.Pro423Thr) | gnomAD v4 |
X | g.41474720C>G | CA412993353 | NYX | c.1252C>G (p.Pro418Ala) c.1267C>G (p.Pro423Ala) | |
X | g.41474720C>T | CA412993354 | NYX | c.1252C>T (p.Pro418Ser) c.1267C>T (p.Pro423Ser) | |
X | g.41474721C>A | CA412993356 | NYX | c.1253C>A (p.Pro418Gln) c.1268C>A (p.Pro423Gln) | gnomAD v4 |
X | g.41474721C= | CA2425928190 | NYX | c.1253C= (p.Pro418=) c.1268C= (p.Pro423=) | |
X | g.41474721C>G | CA412993358 | NYX | c.1253C>G (p.Pro418Arg) c.1268C>G (p.Pro423Arg) | dbSNP |
X | g.41474721C>T | CA412993360 | NYX | c.1253C>T (p.Pro418Leu) c.1268C>T (p.Pro423Leu) | ClinVar gnomAD v4 |
X | g.41474722G>A | CA10389935 | NYX | c.1254G>A (p.Pro418=) c.1269G>A (p.Pro423=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
X | g.41474722G>C | CA516366499 | NYX | c.1254G>C (p.Pro418=) c.1269G>C (p.Pro423=) | |
X | g.41474722G= | CA2425928191 | NYX | c.1254G= (p.Pro418=) c.1269G= (p.Pro423=) | |
X | g.41474722G>T | CA516366500 | NYX | c.1254G>T (p.Pro418=) c.1269G>T (p.Pro423=) | gnomAD v4 |
X | g.41474723A>C | CA516366516 | NYX | c.1255A>C (p.Arg419=) c.1270A>C (p.Arg424=) | |
X | g.41474723A>G | CA412993363 | NYX | c.1255A>G (p.Arg419Gly) c.1270A>G (p.Arg424Gly) | |
X | g.41474723A>T | CA412993364 | NYX | c.1255A>T (p.Arg419Trp) c.1270A>T (p.Arg424Trp) | gnomAD v4 |