Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.173903892_173903895dupCA2649174129SERPINC1c.1392_1395dup (n.1392_1395dup)
c.777_780dup (n.777_780dup)
c.1248_1251dup (n.1248_1251dup)
c.1515_1518dup (n.1515_1518dup)
c.1473_1476dup (n.1473_1476dup)
c.1371_1374dup (n.1371_1374dup)
c.1335_1338dup (n.1335_1338dup)
c.1176_1179dup (n.1176_1179dup)
gnomAD v4
1g.173903892_173903895delCA2586967694SERPINC1c.1392_1395del (p.Ter465MetextTer14)
c.777_780del (p.Ter260MetextTer14)
c.1248_1251del (p.Ter417MetextTer14)
c.1515_1518del (p.Ter506MetextTer14)
c.1473_1476del (p.Ter492MetextTer14)
c.1371_1374del (p.Ter458MetextTer14)
c.1335_1338del (p.Ter446MetextTer14)
c.1176_1179del (p.Ter393MetextTer14)
1g.173903892_173903897delCA2572092707SERPINC1c.1387_1392del (p.Val463_Lys464del)
c.772_777del (p.Val258_Lys259del)
c.1243_1248del (p.Val415_Lys416del)
c.1510_1515del (p.Val504_Lys505del)
c.1468_1473del (p.Val490_Lys491del)
c.1366_1371del (p.Val456_Lys457del)
c.1330_1335del (p.Val444_Lys445del)
c.1171_1176del (p.Val391_Lys392del)
1g.173903893T>ACA343771993SERPINC1c.1391A>T (p.Lys464Met)
c.776A>T (p.Lys259Met)
c.1247A>T (p.Lys416Met)
c.1514A>T (p.Lys505Met)
c.1472A>T (p.Lys491Met)
c.1370A>T (p.Lys457Met)
c.1334A>T (p.Lys445Met)
c.1175A>T (p.Lys392Met)
1g.173903893T>CCA343771994SERPINC1c.1391A>G (p.Lys464Arg)
c.776A>G (p.Lys259Arg)
c.1247A>G (p.Lys416Arg)
c.1514A>G (p.Lys505Arg)
c.1472A>G (p.Lys491Arg)
c.1370A>G (p.Lys457Arg)
c.1334A>G (p.Lys445Arg)
c.1175A>G (p.Lys392Arg)
1g.173903893T>GCA343771995SERPINC1c.1391A>C (p.Lys464Thr)
c.776A>C (p.Lys259Thr)
c.1247A>C (p.Lys416Thr)
c.1514A>C (p.Lys505Thr)
c.1472A>C (p.Lys491Thr)
c.1370A>C (p.Lys457Thr)
c.1334A>C (p.Lys445Thr)
c.1175A>C (p.Lys392Thr)
1g.173903894dupCA2586967696SERPINC1c.1391dup (p.Ter465ValextTer19)
c.776dup (p.Ter260ValextTer19)
c.1247dup (p.Ter417ValextTer19)
c.1514dup (p.Ter506ValextTer19)
c.1472dup (p.Ter492ValextTer19)
c.1370dup (p.Ter458ValextTer19)
c.1334dup (p.Ter446ValextTer19)
c.1175dup (p.Ter393ValextTer19)
1g.173903893_173903894dupCA2586967695SERPINC1c.1390_1391dup (p.Ter465SerextTer16)
c.775_776dup (p.Ter260SerextTer16)
c.1246_1247dup (p.Ter417SerextTer16)
c.1513_1514dup (p.Ter506SerextTer16)
c.1471_1472dup (p.Ter492SerextTer16)
c.1369_1370dup (p.Ter458SerextTer16)
c.1333_1334dup (p.Ter446SerextTer16)
c.1174_1175dup (p.Ter393SerextTer16)
1g.173903894T>ACA343771998SERPINC1c.1390A>T (p.Lys464Ter)
c.775A>T (p.Lys259Ter)
c.1246A>T (p.Lys416Ter)
c.1513A>T (p.Lys505Ter)
c.1471A>T (p.Lys491Ter)
c.1369A>T (p.Lys457Ter)
c.1333A>T (p.Lys445Ter)
c.1174A>T (p.Lys392Ter)
1g.173903894T>CCA343772000SERPINC1c.1390A>G (p.Lys464Glu)
c.775A>G (p.Lys259Glu)
c.1246A>G (p.Lys416Glu)
c.1513A>G (p.Lys505Glu)
c.1471A>G (p.Lys491Glu)
c.1369A>G (p.Lys457Glu)
c.1333A>G (p.Lys445Glu)
c.1174A>G (p.Lys392Glu)
1g.173903894T>GCA343772001SERPINC1c.1390A>C (p.Lys464Gln)
c.775A>C (p.Lys259Gln)
c.1246A>C (p.Lys416Gln)
c.1513A>C (p.Lys505Gln)
c.1471A>C (p.Lys491Gln)
c.1369A>C (p.Lys457Gln)
c.1333A>C (p.Lys445Gln)
c.1174A>C (p.Lys392Gln)
1g.173903894T=CA1207934359SERPINC1c.1390A= (p.Lys464=)
c.775A= (p.Lys259=)
c.1246A= (p.Lys416=)
c.1513A= (p.Lys505=)
c.1471A= (p.Lys491=)
c.1369A= (p.Lys457=)
c.1333A= (p.Lys445=)
c.1174A= (p.Lys392=)
1g.173903895A>CCA421821152SERPINC1c.1389T>G (p.Val463=)
c.774T>G (p.Val258=)
c.1245T>G (p.Val415=)
c.1512T>G (p.Val504=)
c.1470T>G (p.Val490=)
c.1368T>G (p.Val456=)
c.1332T>G (p.Val444=)
c.1173T>G (p.Val391=)
1g.173903895A>GCA421821154SERPINC1c.1389T>C (p.Val463=)
c.774T>C (p.Val258=)
c.1245T>C (p.Val415=)
c.1512T>C (p.Val504=)
c.1470T>C (p.Val490=)
c.1368T>C (p.Val456=)
c.1332T>C (p.Val444=)
c.1173T>C (p.Val391=)
COSMIC
1g.173903895A>TCA421821156SERPINC1c.1389T>A (p.Val463=)
c.774T>A (p.Val258=)
c.1245T>A (p.Val415=)
c.1512T>A (p.Val504=)
c.1470T>A (p.Val490=)
c.1368T>A (p.Val456=)
c.1332T>A (p.Val444=)
c.1173T>A (p.Val391=)
1g.173903895_173903898dupCA527601309SERPINC1c.1386_1389dup (p.Lys464CysfsTer2)
c.771_774dup (p.Lys259CysfsTer2)
c.1242_1245dup (p.Lys416CysfsTer2)
c.1509_1512dup (p.Lys505CysfsTer2)
c.1467_1470dup (p.Lys491CysfsTer2)
c.1365_1368dup (p.Lys457CysfsTer2)
c.1329_1332dup (p.Lys445CysfsTer2)
c.1170_1173dup (p.Lys392CysfsTer2)
dbSNP gnomAD v2 gnomAD v4
1g.173903896A>CCA343772006SERPINC1c.1388T>G (p.Val463Gly)
c.773T>G (p.Val258Gly)
c.1244T>G (p.Val415Gly)
c.1511T>G (p.Val504Gly)
c.1469T>G (p.Val490Gly)
c.1367T>G (p.Val456Gly)
c.1331T>G (p.Val444Gly)
c.1172T>G (p.Val391Gly)
1g.173903896A>GCA343772007SERPINC1c.1388T>C (p.Val463Ala)
c.773T>C (p.Val258Ala)
c.1244T>C (p.Val415Ala)
c.1511T>C (p.Val504Ala)
c.1469T>C (p.Val490Ala)
c.1367T>C (p.Val456Ala)
c.1331T>C (p.Val444Ala)
c.1172T>C (p.Val391Ala)
ClinVar gnomAD v4
1g.173903896A>TCA343772004SERPINC1c.1388T>A (p.Val463Asp)
c.773T>A (p.Val258Asp)
c.1244T>A (p.Val415Asp)
c.1511T>A (p.Val504Asp)
c.1469T>A (p.Val490Asp)
c.1367T>A (p.Val456Asp)
c.1331T>A (p.Val444Asp)
c.1172T>A (p.Val391Asp)
1g.173903897C>ACA343772010SERPINC1c.1387G>T (p.Val463Phe)
c.772G>T (p.Val258Phe)
c.1243G>T (p.Val415Phe)
c.1510G>T (p.Val504Phe)
c.1468G>T (p.Val490Phe)
c.1366G>T (p.Val456Phe)
c.1330G>T (p.Val444Phe)
c.1171G>T (p.Val391Phe)
1g.173903897C>GCA343772012SERPINC1c.1387G>C (p.Val463Leu)
c.772G>C (p.Val258Leu)
c.1243G>C (p.Val415Leu)
c.1510G>C (p.Val504Leu)
c.1468G>C (p.Val490Leu)
c.1366G>C (p.Val456Leu)
c.1330G>C (p.Val444Leu)
c.1171G>C (p.Val391Leu)
1g.173903897C>TCA343772014SERPINC1c.1387G>A (p.Val463Ile)
c.772G>A (p.Val258Ile)
c.1243G>A (p.Val415Ile)
c.1510G>A (p.Val504Ile)
c.1468G>A (p.Val490Ile)
c.1366G>A (p.Val456Ile)
c.1330G>A (p.Val444Ile)
c.1171G>A (p.Val391Ile)
1g.173903898A>CCA343772015SERPINC1c.1386T>G (p.Cys462Trp)
c.771T>G (p.Cys257Trp)
c.1242T>G (p.Cys414Trp)
c.1509T>G (p.Cys503Trp)
c.1467T>G (p.Cys489Trp)
c.1365T>G (p.Cys455Trp)
c.1329T>G (p.Cys443Trp)
c.1170T>G (p.Cys390Trp)
1g.173903898A>GCA421821167SERPINC1c.1386T>C (p.Cys462=)
c.771T>C (p.Cys257=)
c.1242T>C (p.Cys414=)
c.1509T>C (p.Cys503=)
c.1467T>C (p.Cys489=)
c.1365T>C (p.Cys455=)
c.1329T>C (p.Cys443=)
c.1170T>C (p.Cys390=)
1g.173903898A>TCA343772017SERPINC1c.1386T>A (p.Cys462Ter)
c.771T>A (p.Cys257Ter)
c.1242T>A (p.Cys414Ter)
c.1509T>A (p.Cys503Ter)
c.1467T>A (p.Cys489Ter)
c.1365T>A (p.Cys455Ter)
c.1329T>A (p.Cys443Ter)
c.1170T>A (p.Cys390Ter)
1g.173903899C>ACA343772020SERPINC1c.1385G>T (p.Cys462Phe)
c.770G>T (p.Cys257Phe)
c.1241G>T (p.Cys414Phe)
c.1508G>T (p.Cys503Phe)
c.1466G>T (p.Cys489Phe)
c.1364G>T (p.Cys455Phe)
c.1328G>T (p.Cys443Phe)
c.1169G>T (p.Cys390Phe)
1g.173903899C>GCA343772021SERPINC1c.1385G>C (p.Cys462Ser)
c.770G>C (p.Cys257Ser)
c.1241G>C (p.Cys414Ser)
c.1508G>C (p.Cys503Ser)
c.1466G>C (p.Cys489Ser)
c.1364G>C (p.Cys455Ser)
c.1328G>C (p.Cys443Ser)
c.1169G>C (p.Cys390Ser)
1g.173903899C>TCA343772023SERPINC1c.1385G>A (p.Cys462Tyr)
c.770G>A (p.Cys257Tyr)
c.1241G>A (p.Cys414Tyr)
c.1508G>A (p.Cys503Tyr)
c.1466G>A (p.Cys489Tyr)
c.1364G>A (p.Cys455Tyr)
c.1328G>A (p.Cys443Tyr)
c.1169G>A (p.Cys390Tyr)
1g.173903900A>CCA343772026SERPINC1c.1384T>G (p.Cys462Gly)
c.769T>G (p.Cys257Gly)
c.1240T>G (p.Cys414Gly)
c.1507T>G (p.Cys503Gly)
c.1465T>G (p.Cys489Gly)
c.1363T>G (p.Cys455Gly)
c.1327T>G (p.Cys443Gly)
c.1168T>G (p.Cys390Gly)
1g.173903900A>GCA343772027SERPINC1c.1384T>C (p.Cys462Arg)
c.769T>C (p.Cys257Arg)
c.1240T>C (p.Cys414Arg)
c.1507T>C (p.Cys503Arg)
c.1465T>C (p.Cys489Arg)
c.1363T>C (p.Cys455Arg)
c.1327T>C (p.Cys443Arg)
c.1168T>C (p.Cys390Arg)
gnomAD v4
1g.173903900A>TCA343772029SERPINC1c.1384T>A (p.Cys462Ser)
c.769T>A (p.Cys257Ser)
c.1240T>A (p.Cys414Ser)
c.1507T>A (p.Cys503Ser)
c.1465T>A (p.Cys489Ser)
c.1363T>A (p.Cys455Ser)
c.1327T>A (p.Cys443Ser)
c.1168T>A (p.Cys390Ser)
1g.173903900_173903911delCA2586967697SERPINC1c.1373_1384del (p.Val458_Cys462delinsGly)
c.758_769del (p.Val253_Cys257delinsGly)
c.1229_1240del (p.Val410_Cys414delinsGly)
c.1496_1507del (p.Val499_Cys503delinsGly)
c.1454_1465del (p.Val485_Cys489delinsGly)
c.1352_1363del (p.Val451_Cys455delinsGly)
c.1316_1327del (p.Val439_Cys443delinsGly)
c.1157_1168del (p.Val386_Cys390delinsGly)
1g.173903901A=CA1143974262SERPINC1c.1383T= (p.Pro461=)
c.768T= (p.Pro256=)
c.1239T= (p.Pro413=)
c.1506T= (p.Pro502=)
c.1464T= (p.Pro488=)
c.1362T= (p.Pro454=)
c.1326T= (p.Pro442=)
c.1167T= (p.Pro389=)
1g.173903901A>CCA421821176SERPINC1c.1383T>G (p.Pro461=)
c.768T>G (p.Pro256=)
c.1239T>G (p.Pro413=)
c.1506T>G (p.Pro502=)
c.1464T>G (p.Pro488=)
c.1362T>G (p.Pro454=)
c.1326T>G (p.Pro442=)
c.1167T>G (p.Pro389=)
1g.173903901A>GCA32777219SERPINC1c.1383T>C (p.Pro461=)
c.768T>C (p.Pro256=)
c.1239T>C (p.Pro413=)
c.1506T>C (p.Pro502=)
c.1464T>C (p.Pro488=)
c.1362T>C (p.Pro454=)
c.1326T>C (p.Pro442=)
c.1167T>C (p.Pro389=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.173903901A>TCA421821179SERPINC1c.1383T>A (p.Pro461=)
c.768T>A (p.Pro256=)
c.1239T>A (p.Pro413=)
c.1506T>A (p.Pro502=)
c.1464T>A (p.Pro488=)
c.1362T>A (p.Pro454=)
c.1326T>A (p.Pro442=)
c.1167T>A (p.Pro389=)
1g.173903901_173903909delCA2582342991SERPINC1c.1375_1383del (p.Ala459_Pro461del)
c.760_768del (p.Ala254_Pro256del)
c.1231_1239del (p.Ala411_Pro413del)
c.1498_1506del (p.Ala500_Pro502del)
c.1456_1464del (p.Ala486_Pro488del)
c.1354_1362del (p.Ala452_Pro454del)
c.1318_1326del (p.Ala440_Pro442del)
c.1159_1167del (p.Ala387_Pro389del)
1g.173903902G>ACA210781SERPINC1c.1382C>T (p.Pro461Leu)
c.767C>T (p.Pro256Leu)
c.1238C>T (p.Pro413Leu)
c.1505C>T (p.Pro502Leu)
c.1463C>T (p.Pro488Leu)
c.1361C>T (p.Pro454Leu)
c.1325C>T (p.Pro442Leu)
c.1166C>T (p.Pro389Leu)
ClinVar dbSNP gnomAD v4
1g.173903902G>CCA343772036SERPINC1c.1382C>G (p.Pro461Arg)
c.767C>G (p.Pro256Arg)
c.1238C>G (p.Pro413Arg)
c.1505C>G (p.Pro502Arg)
c.1463C>G (p.Pro488Arg)
c.1361C>G (p.Pro454Arg)
c.1325C>G (p.Pro442Arg)
c.1166C>G (p.Pro389Arg)
1g.173903902G=CA1141581217SERPINC1c.1382C= (p.Pro461=)
c.767C= (p.Pro256=)
c.1238C= (p.Pro413=)
c.1505C= (p.Pro502=)
c.1463C= (p.Pro488=)
c.1361C= (p.Pro454=)
c.1325C= (p.Pro442=)
c.1166C= (p.Pro389=)
1g.173903902G>TCA343772033SERPINC1c.1382C>A (p.Pro461His)
c.767C>A (p.Pro256His)
c.1238C>A (p.Pro413His)
c.1505C>A (p.Pro502His)
c.1463C>A (p.Pro488His)
c.1361C>A (p.Pro454His)
c.1325C>A (p.Pro442His)
c.1166C>A (p.Pro389His)
1g.173903903G>ACA343772038SERPINC1c.1381C>T (p.Pro461Ser)
c.766C>T (p.Pro256Ser)
c.1237C>T (p.Pro413Ser)
c.1504C>T (p.Pro502Ser)
c.1462C>T (p.Pro488Ser)
c.1360C>T (p.Pro454Ser)
c.1324C>T (p.Pro442Ser)
c.1165C>T (p.Pro389Ser)
COSMIC
1g.173903903G>CCA343772040SERPINC1c.1381C>G (p.Pro461Ala)
c.766C>G (p.Pro256Ala)
c.1237C>G (p.Pro413Ala)
c.1504C>G (p.Pro502Ala)
c.1462C>G (p.Pro488Ala)
c.1360C>G (p.Pro454Ala)
c.1324C>G (p.Pro442Ala)
c.1165C>G (p.Pro389Ala)
1g.173903903G>TCA343772042SERPINC1c.1381C>A (p.Pro461Thr)
c.766C>A (p.Pro256Thr)
c.1237C>A (p.Pro413Thr)
c.1504C>A (p.Pro502Thr)
c.1462C>A (p.Pro488Thr)
c.1360C>A (p.Pro454Thr)
c.1324C>A (p.Pro442Thr)
c.1165C>A (p.Pro389Thr)
gnomAD v4
1g.173903903_173903911delCA2499214317SERPINC1c.1373_1381del (p.Val458_Pro461delinsAla)
c.758_766del (p.Val253_Pro256delinsAla)
c.1229_1237del (p.Val410_Pro413delinsAla)
c.1496_1504del (p.Val499_Pro502delinsAla)
c.1454_1462del (p.Val485_Pro488delinsAla)
c.1352_1360del (p.Val451_Pro454delinsAla)
c.1316_1324del (p.Val439_Pro442delinsAla)
c.1157_1165del (p.Val386_Pro389delinsAla)
ClinVar dbSNP
1g.173903904G>ACA421821191SERPINC1c.1380C>T (p.Asn460=)
c.765C>T (p.Asn255=)
c.1236C>T (p.Asn412=)
c.1503C>T (p.Asn501=)
c.1461C>T (p.Asn487=)
c.1359C>T (p.Asn453=)
c.1323C>T (p.Asn441=)
c.1164C>T (p.Asn388=)
1g.173903904G>CCA343772045SERPINC1c.1380C>G (p.Asn460Lys)
c.765C>G (p.Asn255Lys)
c.1236C>G (p.Asn412Lys)
c.1503C>G (p.Asn501Lys)
c.1461C>G (p.Asn487Lys)
c.1359C>G (p.Asn453Lys)
c.1323C>G (p.Asn441Lys)
c.1164C>G (p.Asn388Lys)
1g.173903904G>TCA343772047SERPINC1c.1380C>A (p.Asn460Lys)
c.765C>A (p.Asn255Lys)
c.1236C>A (p.Asn412Lys)
c.1503C>A (p.Asn501Lys)
c.1461C>A (p.Asn487Lys)
c.1359C>A (p.Asn453Lys)
c.1323C>A (p.Asn441Lys)
c.1164C>A (p.Asn388Lys)
gnomAD v4
1g.173903905T>ACA343772053SERPINC1c.1379A>T (p.Asn460Ile)
c.764A>T (p.Asn255Ile)
c.1235A>T (p.Asn412Ile)
c.1502A>T (p.Asn501Ile)
c.1460A>T (p.Asn487Ile)
c.1358A>T (p.Asn453Ile)
c.1322A>T (p.Asn441Ile)
c.1163A>T (p.Asn388Ile)
1g.173903905T>CCA343772050SERPINC1c.1379A>G (p.Asn460Ser)
c.764A>G (p.Asn255Ser)
c.1235A>G (p.Asn412Ser)
c.1502A>G (p.Asn501Ser)
c.1460A>G (p.Asn487Ser)
c.1358A>G (p.Asn453Ser)
c.1322A>G (p.Asn441Ser)
c.1163A>G (p.Asn388Ser)

Number of alleles fetched