| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 12 | g.102840395_102840401del | CA912973337 | PAH | c.1314_1315+5del c.1299_1300+5del n.976_977+5del c.418_419+5del n.829_830+5del c.1257_1258+5del | |
| 12 | g.102840395_102840401delinsCTTACTG | CA2059441378 | PAH | c.1314_1315+5delinsCAGTAAG c.1299_1300+5delinsCAGTAAG n.976_977+5delinsCAGTAAG c.418_419+5delinsCAGTAAG n.829_830+5delinsCAGTAAG c.1257_1258+5delinsCAGTAAG | |
| 12 | g.102840399_102840404del | CA16020994 | PAH | c.1314_1315+4del c.1299_1300+4del n.976_977+4del c.418_419+4del n.829_830+4del c.1257_1258+4del | ClinVar dbSNP |
| 12 | g.102840400T>A | CA386492912 | PAH | c.1315A>T (p.Ser439Cys) c.1300A>T (p.Ser434Cys) n.977A>T c.419A>T n.830A>T c.1258A>T (p.Ser420Cys) | |
| 12 | g.102840400T>C | CA242743409 | PAH | c.1315A>G (p.Ser439Gly) c.1300A>G (p.Ser434Gly) n.977A>G c.419A>G n.830A>G c.1258A>G (p.Ser420Gly) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 12 | g.102840400T>G | CA386492913 | PAH | c.1315A>C (p.Ser439Arg) c.1300A>C (p.Ser434Arg) n.977A>C c.419A>C n.830A>C c.1258A>C (p.Ser420Arg) | |
| 12 | g.102840400T= | CA2059441448 | PAH | c.1315A= (p.Ser439=) c.1300A= (p.Ser434=) n.977A= c.419A= n.830A= c.1258A= (p.Ser420=) | |
| 12 | g.102840401G>A | CA242743411 | PAH | c.1314C>T (p.Asn438=) c.1299C>T (p.Asn433=) n.976C>T c.418C>T n.829C>T c.1257C>T (p.Asn419=) | dbSNP |
| 12 | g.102840401G>C | CA386492914 | PAH | c.1314C>G (p.Asn438Lys) c.1299C>G (p.Asn433Lys) n.976C>G c.418C>G n.829C>G c.1257C>G (p.Asn419Lys) | |
| 12 | g.102840401G= | CA2059441455 | PAH | c.1314C= (p.Asn438=) c.1299C= (p.Asn433=) n.976C= c.418C= n.829C= c.1257C= (p.Asn419=) | |
| 12 | g.102840401G>T | CA386492915 | PAH | c.1314C>A (p.Asn438Lys) c.1299C>A (p.Asn433Lys) n.976C>A c.418C>A n.829C>A c.1257C>A (p.Asn419Lys) | |
| 12 | g.102840402T>A | CA386492916 | PAH | c.1313A>T (p.Asn438Ile) c.1298A>T (p.Asn433Ile) n.975A>T c.417A>T n.828A>T c.1256A>T (p.Asn419Ile) | |
| 12 | g.102840402T>C | CA386492917 | PAH | c.1313A>G (p.Asn438Ser) c.1298A>G (p.Asn433Ser) n.975A>G c.417A>G n.828A>G c.1256A>G (p.Asn419Ser) | gnomAD v4 |
| 12 | g.102840402T>G | CA386492918 | PAH | c.1313A>C (p.Asn438Thr) c.1298A>C (p.Asn433Thr) n.975A>C c.417A>C n.828A>C c.1256A>C (p.Asn419Thr) | |
| 12 | g.102840403T>A | CA386492919 | PAH | c.1312A>T (p.Asn438Tyr) c.1297A>T (p.Asn433Tyr) n.974A>T c.416A>T n.827A>T c.1255A>T (p.Asn419Tyr) | |
| 12 | g.102840403T>C | CA16020992 | PAH | c.1312A>G (p.Asn438Asp) c.1297A>G (p.Asn433Asp) n.974A>G c.416A>G n.827A>G c.1255A>G (p.Asn419Asp) | ClinVar dbSNP |
| 12 | g.102840403T>G | CA386492920 | PAH | c.1312A>C (p.Asn438His) c.1297A>C (p.Asn433His) n.974A>C c.416A>C n.827A>C c.1255A>C (p.Asn419His) | |
| 12 | g.102840403T= | CA2059441462 | PAH | c.1312A= (p.Asn438=) c.1297A= (p.Asn433=) n.974A= c.416A= n.827A= c.1255A= (p.Asn419=) | |
| 12 | g.102840404A>C | CA386492921 | PAH | c.1311T>G (p.Ile437Met) c.1296T>G (p.Ile432Met) n.973T>G c.415T>G n.826T>G c.1254T>G (p.Ile418Met) | |
| 12 | g.102840404A>G | CA481375324 | PAH | c.1311T>C (p.Ile437=) c.1296T>C (p.Ile432=) n.973T>C c.415T>C n.826T>C c.1254T>C (p.Ile418=) | gnomAD v4 |
| 12 | g.102840404A>T | CA481375323 | PAH | c.1311T>A (p.Ile437=) c.1296T>A (p.Ile432=) n.973T>A c.415T>A n.826T>A c.1254T>A (p.Ile418=) | gnomAD v4 |
| 12 | g.102840405A>C | CA386492922 | PAH | c.1310T>G (p.Ile437Ser) c.1295T>G (p.Ile432Ser) n.972T>G c.414T>G n.825T>G c.1253T>G (p.Ile418Ser) | |
| 12 | g.102840405A>G | CA386492923 | PAH | c.1310T>C (p.Ile437Thr) c.1295T>C (p.Ile432Thr) n.972T>C c.414T>C n.825T>C c.1253T>C (p.Ile418Thr) | |
| 12 | g.102840405A>T | CA386492924 | PAH | c.1310T>A (p.Ile437Asn) c.1295T>A (p.Ile432Asn) n.972T>A c.414T>A n.825T>A c.1253T>A (p.Ile418Asn) | |
| 12 | g.102840406T>A | CA386492925 | PAH | c.1309A>T (p.Ile437Phe) c.1294A>T (p.Ile432Phe) n.971A>T c.413A>T n.824A>T c.1252A>T (p.Ile418Phe) | |
| 12 | g.102840406T>C | CA386492927 | PAH | c.1309A>G (p.Ile437Val) c.1294A>G (p.Ile432Val) n.971A>G c.413A>G n.824A>G c.1252A>G (p.Ile418Val) | gnomAD v4 |
| 12 | g.102840406T>G | CA386492926 | PAH | c.1309A>C (p.Ile437Leu) c.1294A>C (p.Ile432Leu) n.971A>C c.413A>C n.824A>C c.1252A>C (p.Ile418Leu) | |
| 12 | g.102840407G>A | CA242743413 | PAH | c.1308C>T (p.Ser436=) c.1293C>T (p.Ser431=) n.970C>T c.412C>T n.823C>T c.1251C>T (p.Ser417=) | dbSNP COSMIC |
| 12 | g.102840407G>C | CA481375325 | PAH | c.1308C>G (p.Ser436=) c.1293C>G (p.Ser431=) n.970C>G c.412C>G n.823C>G c.1251C>G (p.Ser417=) | |
| 12 | g.102840407G= | CA2059441470 | PAH | c.1308C= (p.Ser436=) c.1293C= (p.Ser431=) n.970C= c.412C= n.823C= c.1251C= (p.Ser417=) | |
| 12 | g.102840407G>T | CA481375326 | PAH | c.1308C>A (p.Ser436=) c.1293C>A (p.Ser431=) n.970C>A c.412C>A n.823C>A c.1251C>A (p.Ser417=) | |
| 12 | g.102840408G>A | CA242743415 | PAH | c.1307C>T (p.Ser436Phe) c.1292C>T (p.Ser431Phe) n.969C>T c.411C>T n.822C>T c.1250C>T (p.Ser417Phe) | dbSNP |
| 12 | g.102840408G>C | CA386492928 | PAH | c.1307C>G (p.Ser436Cys) c.1292C>G (p.Ser431Cys) n.969C>G c.411C>G n.822C>G c.1250C>G (p.Ser417Cys) | |
| 12 | g.102840408G= | CA2059441480 | PAH | c.1307C= (p.Ser436=) c.1292C= (p.Ser431=) n.969C= c.411C= n.822C= c.1250C= (p.Ser417=) | |
| 12 | g.102840408G>T | CA386492929 | PAH | c.1307C>A (p.Ser436Tyr) c.1292C>A (p.Ser431Tyr) n.969C>A c.411C>A n.822C>A c.1250C>A (p.Ser417Tyr) | COSMIC |
| 12 | g.102840408_102840409delinsGA | CA2059441483 | PAH | c.1306_1307delinsTC (p.Ser436=) c.1291_1292delinsTC (p.Ser431=) n.968_969delinsTC c.410_411delinsTC n.821_822delinsTC c.1249_1250delinsTC (p.Ser417=) | |
| 12 | g.102840409A>C | CA386492930 | PAH | c.1306T>G (p.Ser436Ala) c.1291T>G (p.Ser431Ala) n.968T>G c.410T>G n.821T>G c.1249T>G (p.Ser417Ala) | |
| 12 | g.102840409A>G | CA386492931 | PAH | c.1306T>C (p.Ser436Pro) c.1291T>C (p.Ser431Pro) n.968T>C c.410T>C n.821T>C c.1249T>C (p.Ser417Pro) | |
| 12 | g.102840409A>T | CA386492932 | PAH | c.1306T>A (p.Ser436Thr) c.1291T>A (p.Ser431Thr) n.968T>A c.410T>A n.821T>A c.1249T>A (p.Ser417Thr) | |
| 12 | g.102840410del | CA16020991 | PAH | c.1306del (p.Ser436ProfsTer16) c.1291del (p.Ser431ProfsTer16) n.968del c.410del n.821del c.1249del (p.Ser417ProfsTer16) | ClinVar dbSNP |
| 12 | g.102840410A= | CA2059441506 | PAH | c.1305T= (p.Asp435=) c.1290T= (p.Asp430=) n.967T= c.409T= n.820T= c.1248T= (p.Asp416=) | |
| 12 | g.102840410A>C | CA386492933 | PAH | c.1305T>G (p.Asp435Glu) c.1290T>G (p.Asp430Glu) n.967T>G c.409T>G n.820T>G c.1248T>G (p.Asp416Glu) | dbSNP |
| 12 | g.102840410A>G | CA481375328 | PAH | c.1305T>C (p.Asp435=) c.1290T>C (p.Asp430=) n.967T>C c.409T>C n.820T>C c.1248T>C (p.Asp416=) | ClinVar |
| 12 | g.102840410A>T | CA6748699 | PAH | c.1305T>A (p.Asp435Glu) c.1290T>A (p.Asp430Glu) n.967T>A c.409T>A n.820T>A c.1248T>A (p.Asp416Glu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 12 | g.102840411T>A | CA386492936 | PAH | c.1304A>T (p.Asp435Val) c.1289A>T (p.Asp430Val) n.966A>T c.408A>T n.819A>T c.1247A>T (p.Asp416Val) | ClinVar dbSNP gnomAD v4 |
| 12 | g.102840411T>C | CA386492935 | PAH | c.1304A>G (p.Asp435Gly) c.1289A>G (p.Asp430Gly) n.966A>G c.408A>G n.819A>G c.1247A>G (p.Asp416Gly) | |
| 12 | g.102840411T>G | CA386492934 | PAH | c.1304A>C (p.Asp435Ala) c.1289A>C (p.Asp430Ala) n.966A>C c.408A>C n.819A>C c.1247A>C (p.Asp416Ala) | |
| 12 | g.102840411T= | CA2059441507 | PAH | c.1304A= (p.Asp435=) c.1289A= (p.Asp430=) n.966A= c.408A= n.819A= c.1247A= (p.Asp416=) | |
| 12 | g.102840412C>A | CA386492937 | PAH | c.1303G>T (p.Asp435Tyr) c.1288G>T (p.Asp430Tyr) n.965G>T c.407G>T n.818G>T c.1246G>T (p.Asp416Tyr) | |
| 12 | g.102840412C>G | CA386492938 | PAH | c.1303G>C (p.Asp435His) c.1288G>C (p.Asp430His) n.965G>C c.407G>C n.818G>C c.1246G>C (p.Asp416His) |