Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.68685188C=CA2229889193CDH3c.1425-17C= (n.1425-17C=)
c.*1163-17C= (n.*1163-17C=)
c.1260-17C= (n.1260-17C=)
16g.68685188C>GCA283280822CDH3c.1425-17C>G (n.1425-17C>G)
c.*1163-17C>G (n.*1163-17C>G)
c.1260-17C>G (n.1260-17C>G)
 dbSNP gnomAD v4
16g.68685190A>CCA2633931487CDH3c.1425-15A>C (n.1425-15A>C)
c.*1163-15A>C (n.*1163-15A>C)
c.1260-15A>C (n.1260-15A>C)
 gnomAD v4
16g.68685191C=CA2229889194CDH3c.1425-14C= (n.1425-14C=)
c.*1163-14C= (n.*1163-14C=)
c.1260-14C= (n.1260-14C=)
16g.68685191C>TCA978516720CDH3c.1425-14C>T (n.1425-14C>T)
c.*1163-14C>T (n.*1163-14C>T)
c.1260-14C>T (n.1260-14C>T)
 dbSNP gnomAD v3 gnomAD v4
16g.68685192T>CCA2633931488CDH3c.1425-13T>C (n.1425-13T>C)
c.*1163-13T>C (n.*1163-13T>C)
c.1260-13T>C (n.1260-13T>C)
 gnomAD v4
16g.68685195dupCA2633931489CDH3c.1425-10dup (n.1425-10dup)
c.*1163-10dup (n.*1163-10dup)
c.1260-10dup (n.1260-10dup)
 gnomAD v4
16g.68685195delCA2633931490CDH3c.1425-10del (n.1425-10del)
c.*1163-10del (n.*1163-10del)
c.1260-10del (n.1260-10del)
 gnomAD v4
16g.68685193T>ACA2576038380CDH3c.1425-12T>A (n.1425-12T>A)
c.*1163-12T>A (n.*1163-12T>A)
c.1260-12T>A (n.1260-12T>A)
16g.68685193T>CCA283280828CDH3c.1425-12T>C (n.1425-12T>C)
c.*1163-12T>C (n.*1163-12T>C)
c.1260-12T>C (n.1260-12T>C)
 dbSNP gnomAD v2 gnomAD v4
16g.68685193T=CA2229889195CDH3c.1425-12T= (n.1425-12T=)
c.*1163-12T= (n.*1163-12T=)
c.1260-12T= (n.1260-12T=)
16g.68685194T>CCA2633931491CDH3c.1425-11T>C (n.1425-11T>C)
c.*1163-11T>C (n.*1163-11T>C)
c.1260-11T>C (n.1260-11T>C)
 gnomAD v4
16g.68685195T>CCA2633931492CDH3c.1425-10T>C (n.1425-10T>C)
c.*1163-10T>C (n.*1163-10T>C)
c.1260-10T>C (n.1260-10T>C)
 gnomAD v4
16g.68685196C>ACA2633931493CDH3c.1425-9C>A (n.1425-9C>A)
c.*1163-9C>A (n.*1163-9C>A)
c.1260-9C>A (n.1260-9C>A)
 gnomAD v4
16g.68685196C>TCA2576038381CDH3c.1425-9C>T (n.1425-9C>T)
c.*1163-9C>T (n.*1163-9C>T)
c.1260-9C>T (n.1260-9C>T)
 gnomAD v4
16g.68685197C=CA2229889196CDH3c.1425-8C= (n.1425-8C=)
c.*1163-8C= (n.*1163-8C=)
c.1260-8C= (n.1260-8C=)
16g.68685197C>GCA978516724CDH3c.1425-8C>G (n.1425-8C>G)
c.*1163-8C>G (n.*1163-8C>G)
c.1260-8C>G (n.1260-8C>G)
 dbSNP gnomAD v3 gnomAD v4
16g.68685198T>ACA283280831CDH3c.1425-7T>A (n.1425-7T>A)
c.*1163-7T>A (n.*1163-7T>A)
c.1260-7T>A (n.1260-7T>A)
 dbSNP gnomAD v4
16g.68685198T=CA2229889198CDH3c.1425-7T= (n.1425-7T=)
c.*1163-7T= (n.*1163-7T=)
c.1260-7T= (n.1260-7T=)
16g.68685199C>ACA2633931494CDH3c.1425-6C>A (n.1425-6C>A)
c.*1163-6C>A (n.*1163-6C>A)
c.1260-6C>A (n.1260-6C>A)
 gnomAD v4
16g.68685199C=CA2229889200CDH3c.1425-6C= (n.1425-6C=)
c.*1163-6C= (n.*1163-6C=)
c.1260-6C= (n.1260-6C=)
16g.68685199C>TCA2229889202CDH3c.1425-6C>T (n.1425-6C>T)
c.*1163-6C>T (n.*1163-6C>T)
c.1260-6C>T (n.1260-6C>T)
 dbSNP gnomAD v4
16g.68685201C>ACA2633931495CDH3c.1425-4C>A (n.1425-4C>A)
c.*1163-4C>A (n.*1163-4C>A)
c.1260-4C>A (n.1260-4C>A)
 gnomAD v4
16g.68685201C>TCA2580092026CDH3c.1425-4C>T (n.1425-4C>T)
c.*1163-4C>T (n.*1163-4C>T)
c.1260-4C>T (n.1260-4C>T)
 ClinVar gnomAD v4
16g.68685203A>CCA396454235CDH3c.1425-2A>C (n.1425-2A>C)
c.*1163-2A>C (n.*1163-2A>C)
c.1260-2A>C (n.1260-2A>C)
16g.68685203A>GCA396454237CDH3c.1425-2A>G (n.1425-2A>G)
c.*1163-2A>G (n.*1163-2A>G)
c.1260-2A>G (n.1260-2A>G)
16g.68685203A>TCA396454236CDH3c.1425-2A>T (n.1425-2A>T)
c.*1163-2A>T (n.*1163-2A>T)
c.1260-2A>T (n.1260-2A>T)
16g.68685204G>ACA396454238CDH3c.1425-1G>A (n.1425-1G>A)
c.*1163-1G>A (n.*1163-1G>A)
c.1260-1G>A (n.1260-1G>A)
16g.68685204G>CCA396454239CDH3c.1425-1G>C (n.1425-1G>C)
c.*1163-1G>C (n.*1163-1G>C)
c.1260-1G>C (n.1260-1G>C)
16g.68685204G=CA2229889203CDH3c.1425-1G= (n.1425-1G=)
c.*1163-1G= (n.*1163-1G=)
c.1260-1G= (n.1260-1G=)
16g.68685204G>TCA8129364CDH3c.1425-1G>T (n.1425-1G>T)
c.*1163-1G>T (n.*1163-1G>T)
c.1260-1G>T (n.1260-1G>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.68685205C>ACA396454240CDH3c.1425C>A (p.Ser475Arg)
c.*1163C>A (n.*1163C>A)
c.1260C>A (p.Ser420Arg)
16g.68685205C=CA2229889204CDH3c.1425C= (p.Ser475=)
c.*1163C= (n.*1163C=)
c.1260C= (p.Ser420=)
16g.68685205C>GCA396454241CDH3c.1425C>G (p.Ser475Arg)
c.*1163C>G (n.*1163C>G)
c.1260C>G (p.Ser420Arg)
 dbSNP
16g.68685205C>TCA496154434CDH3c.1425C>T (p.Ser475=)
c.*1163C>T (n.*1163C>T)
c.1260C>T (p.Ser420=)
 dbSNP
16g.68685206T>ACA396454242CDH3c.1426T>A (p.Tyr476Asn)
c.*1164T>A (n.*1164T>A)
c.1261T>A (p.Tyr421Asn)
16g.68685206T>CCA396454243CDH3c.1426T>C (p.Tyr476His)
c.*1164T>C (n.*1164T>C)
c.1261T>C (p.Tyr421His)
 gnomAD v4
16g.68685206T>GCA396454244CDH3c.1426T>G (p.Tyr476Asp)
c.*1164T>G (n.*1164T>G)
c.1261T>G (p.Tyr421Asp)
16g.68685207A=CA2229889205CDH3c.1427A= (p.Tyr476=)
c.*1165A= (n.*1165A=)
c.1262A= (p.Tyr421=)
16g.68685207A>CCA396454245CDH3c.1427A>C (p.Tyr476Ser)
c.*1165A>C (n.*1165A>C)
c.1262A>C (p.Tyr421Ser)
 dbSNP
16g.68685207A>GCA396454246CDH3c.1427A>G (p.Tyr476Cys)
c.*1165A>G (n.*1165A>G)
c.1262A>G (p.Tyr421Cys)
16g.68685207A>TCA396454247CDH3c.1427A>T (p.Tyr476Phe)
c.*1165A>T (n.*1165A>T)
c.1262A>T (p.Tyr421Phe)
16g.68685208C>ACA396454248CDH3c.1428C>A (p.Tyr476Ter)
c.*1166C>A (n.*1166C>A)
c.1263C>A (p.Tyr421Ter)
16g.68685208C>GCA396454249CDH3c.1428C>G (p.Tyr476Ter)
c.*1166C>G (n.*1166C>G)
c.1263C>G (p.Tyr421Ter)
16g.68685208C>TCA496154435CDH3c.1428C>T (p.Tyr476=)
c.*1166C>T (n.*1166C>T)
c.1263C>T (p.Tyr421=)
16g.68685209C>ACA396454252CDH3c.1429C>A (p.Arg477Ser)
c.*1167C>A (n.*1167C>A)
c.1264C>A (p.Arg422Ser)
 gnomAD v4
16g.68685209C=CA2229889206CDH3c.1429C= (p.Arg477=)
c.*1167C= (n.*1167C=)
c.1264C= (p.Arg422=)
16g.68685209C>GCA396454251CDH3c.1429C>G (p.Arg477Gly)
c.*1167C>G (n.*1167C>G)
c.1264C>G (p.Arg422Gly)
16g.68685209C>TCA396454250CDH3c.1429C>T (p.Arg477Cys)
c.*1167C>T (n.*1167C>T)
c.1264C>T (p.Arg422Cys)
 ClinVar dbSNP gnomAD v2 gnomAD v4
16g.68685210G>ACA8129365CDH3c.1430G>A (p.Arg477His)
c.*1168G>A (n.*1168G>A)
c.1265G>A (p.Arg422His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.68685210G>CCA396454253CDH3c.1430G>C (p.Arg477Pro)
c.*1168G>C (n.*1168G>C)
c.1265G>C (p.Arg422Pro)
16g.68685210G=CA2229889207CDH3c.1430G= (p.Arg477=)
c.*1168G= (n.*1168G=)
c.1265G= (p.Arg422=)
16g.68685210G>TCA396454254CDH3c.1430G>T (p.Arg477Leu)
c.*1168G>T (n.*1168G>T)
c.1265G>T (p.Arg422Leu)
16g.68685211C>ACA496154436CDH3c.1431C>A (p.Arg477=)
c.*1169C>A (n.*1169C>A)
c.1266C>A (p.Arg422=)
16g.68685211C=CA2229889208CDH3c.1431C= (p.Arg477=)
c.*1169C= (n.*1169C=)
c.1266C= (p.Arg422=)
16g.68685211C>GCA496154437CDH3c.1431C>G (p.Arg477=)
c.*1169C>G (n.*1169C>G)
c.1266C>G (p.Arg422=)
16g.68685211C>TCA496154438CDH3c.1431C>T (p.Arg477=)
c.*1169C>T (n.*1169C>T)
c.1266C>T (p.Arg422=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.68685212A>CCA396454255CDH3c.1432A>C (p.Ile478Leu)
c.*1170A>C (n.*1170A>C)
c.1267A>C (p.Ile423Leu)
16g.68685212A>GCA396454256CDH3c.1432A>G (p.Ile478Val)
c.*1170A>G (n.*1170A>G)
c.1267A>G (p.Ile423Val)
16g.68685212A>TCA396454257CDH3c.1432A>T (p.Ile478Phe)
c.*1170A>T (n.*1170A>T)
c.1267A>T (p.Ile423Phe)
16g.68685213T>ACA396454258CDH3c.1433T>A (p.Ile478Asn)
c.*1171T>A (n.*1171T>A)
c.1268T>A (p.Ile423Asn)
16g.68685213T>CCA396454259CDH3c.1433T>C (p.Ile478Thr)
c.*1171T>C (n.*1171T>C)
c.1268T>C (p.Ile423Thr)
16g.68685213T>GCA396454260CDH3c.1433T>G (p.Ile478Ser)
c.*1171T>G (n.*1171T>G)
c.1268T>G (p.Ile423Ser)
16g.68685214C>ACA496154439CDH3c.1434C>A (p.Ile478=)
c.*1172C>A (n.*1172C>A)
c.1269C>A (p.Ile423=)
16g.68685214C=CA2229889209CDH3c.1434C= (p.Ile478=)
c.*1172C= (n.*1172C=)
c.1269C= (p.Ile423=)
16g.68685214C>GCA396454261CDH3c.1434C>G (p.Ile478Met)
c.*1172C>G (n.*1172C>G)
c.1269C>G (p.Ile423Met)
16g.68685214C>TCA8129366CDH3c.1434C>T (p.Ile478=)
c.*1172C>T (n.*1172C>T)
c.1269C>T (p.Ile423=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.68685215C>ACA396454263CDH3c.1435C>A (p.Leu479Met)
c.*1173C>A (n.*1173C>A)
c.1270C>A (p.Leu424Met)
16g.68685215C>GCA396454262CDH3c.1435C>G (p.Leu479Val)
c.*1173C>G (n.*1173C>G)
c.1270C>G (p.Leu424Val)
16g.68685215C>TCA496154440CDH3c.1435C>T (p.Leu479=)
c.*1173C>T (n.*1173C>T)
c.1270C>T (p.Leu424=)
16g.68685216T>ACA396454264CDH3c.1436T>A (p.Leu479Gln)
c.*1174T>A (n.*1174T>A)
c.1271T>A (p.Leu424Gln)
16g.68685216T>CCA200814CDH3c.1436T>C (p.Leu479Pro)
c.*1174T>C (n.*1174T>C)
c.1271T>C (p.Leu424Pro)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.68685216T>GCA396454265CDH3c.1436T>G (p.Leu479Arg)
c.*1174T>G (n.*1174T>G)
c.1271T>G (p.Leu424Arg)
16g.68685216T=CA2229889210CDH3c.1436T= (p.Leu479=)
c.*1174T= (n.*1174T=)
c.1271T= (p.Leu424=)
16g.68685217G>ACA496154441CDH3c.1437G>A (p.Leu479=)
c.*1175G>A (n.*1175G>A)
c.1272G>A (p.Leu424=)
 ClinVar
16g.68685217G>CCA496154442CDH3c.1437G>C (p.Leu479=)
c.*1175G>C (n.*1175G>C)
c.1272G>C (p.Leu424=)
16g.68685217G>TCA496154443CDH3c.1437G>T (p.Leu479=)
c.*1175G>T (n.*1175G>T)
c.1272G>T (p.Leu424=)
16g.68685218A>CCA496154444CDH3c.1438A>C (p.Arg480=)
c.*1176A>C (n.*1176A>C)
c.1273A>C (p.Arg425=)
 ClinVar
16g.68685218A>GCA396454266CDH3c.1438A>G (p.Arg480Gly)
c.*1176A>G (n.*1176A>G)
c.1273A>G (p.Arg425Gly)
16g.68685218A>TCA396454267CDH3c.1438A>T (p.Arg480Ter)
c.*1176A>T (n.*1176A>T)
c.1273A>T (p.Arg425Ter)
16g.68685219G>ACA396454268CDH3c.1439G>A (p.Arg480Lys)
c.*1177G>A (n.*1177G>A)
c.1274G>A (p.Arg425Lys)
 gnomAD v4
16g.68685219G>CCA396454269CDH3c.1439G>C (p.Arg480Thr)
c.*1177G>C (n.*1177G>C)
c.1274G>C (p.Arg425Thr)
16g.68685219G>TCA396454270CDH3c.1439G>T (p.Arg480Ile)
c.*1177G>T (n.*1177G>T)
c.1274G>T (p.Arg425Ile)
16g.68685220A>CCA396454271CDH3c.1440A>C (p.Arg480Ser)
c.*1178A>C (n.*1178A>C)
c.1275A>C (p.Arg425Ser)
16g.68685220A>GCA496154445CDH3c.1440A>G (p.Arg480=)
c.*1178A>G (n.*1178A>G)
c.1275A>G (p.Arg425=)
16g.68685220A>TCA396454272CDH3c.1440A>T (p.Arg480Ser)
c.*1178A>T (n.*1178A>T)
c.1275A>T (p.Arg425Ser)
16g.68685221G>ACA396454273CDH3c.1441G>A (p.Asp481Asn)
c.*1179G>A (n.*1179G>A)
c.1276G>A (p.Asp426Asn)
 gnomAD v4
16g.68685221G>CCA396454274CDH3c.1441G>C (p.Asp481His)
c.*1179G>C (n.*1179G>C)
c.1276G>C (p.Asp426His)
16g.68685221G>TCA396454275CDH3c.1441G>T (p.Asp481Tyr)
c.*1179G>T (n.*1179G>T)
c.1276G>T (p.Asp426Tyr)
16g.68685222A>CCA396454278CDH3c.1442A>C (p.Asp481Ala)
c.*1180A>C (n.*1180A>C)
c.1277A>C (p.Asp426Ala)
16g.68685222A>GCA396454276CDH3c.1442A>G (p.Asp481Gly)
c.*1180A>G (n.*1180A>G)
c.1277A>G (p.Asp426Gly)
16g.68685222A>TCA396454277CDH3c.1442A>T (p.Asp481Val)
c.*1180A>T (n.*1180A>T)
c.1277A>T (p.Asp426Val)
16g.68685223C>ACA396454279CDH3c.1443C>A (p.Asp481Glu)
c.*1181C>A (n.*1181C>A)
c.1278C>A (p.Asp426Glu)
 gnomAD v4
16g.68685223C=CA2229889211CDH3c.1443C= (p.Asp481=)
c.*1181C= (n.*1181C=)
c.1278C= (p.Asp426=)
16g.68685223C>GCA396454280CDH3c.1443C>G (p.Asp481Glu)
c.*1181C>G (n.*1181C>G)
c.1278C>G (p.Asp426Glu)
16g.68685223C>TCA239524CDH3c.1443C>T (p.Asp481=)
c.*1181C>T (n.*1181C>T)
c.1278C>T (p.Asp426=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.68685224C>ACA396454281CDH3c.1444C>A (p.Pro482Thr)
c.*1182C>A (n.*1182C>A)
c.1279C>A (p.Pro427Thr)
16g.68685224C>GCA396454282CDH3c.1444C>G (p.Pro482Ala)
c.*1182C>G (n.*1182C>G)
c.1279C>G (p.Pro427Ala)
16g.68685224C>TCA396454283CDH3c.1444C>T (p.Pro482Ser)
c.*1182C>T (n.*1182C>T)
c.1279C>T (p.Pro427Ser)
16g.68685225C>ACA396454284CDH3c.1445C>A (p.Pro482Gln)
c.*1183C>A (n.*1183C>A)
c.1280C>A (p.Pro427Gln)
 gnomAD v4
16g.68685225C>GCA396454285CDH3c.1445C>G (p.Pro482Arg)
c.*1183C>G (n.*1183C>G)
c.1280C>G (p.Pro427Arg)
16g.68685225C>TCA396454286CDH3c.1445C>T (p.Pro482Leu)
c.*1183C>T (n.*1183C>T)
c.1280C>T (p.Pro427Leu)
16g.68685226A>CCA496154447CDH3c.1446A>C (p.Pro482=)
c.*1184A>C (n.*1184A>C)
c.1281A>C (p.Pro427=)
16g.68685226A>GCA496154448CDH3c.1446A>G (p.Pro482=)
c.*1184A>G (n.*1184A>G)
c.1281A>G (p.Pro427=)
 gnomAD v4
16g.68685226A>TCA496154449CDH3c.1446A>T (p.Pro482=)
c.*1184A>T (n.*1184A>T)
c.1281A>T (p.Pro427=)
16g.68685227G>ACA396454287CDH3c.1447G>A (p.Ala483Thr)
c.*1185G>A (n.*1185G>A)
c.1282G>A (p.Ala428Thr)
 dbSNP gnomAD v2 gnomAD v4
16g.68685227G>CCA396454288CDH3c.1447G>C (p.Ala483Pro)
c.*1185G>C (n.*1185G>C)
c.1282G>C (p.Ala428Pro)
16g.68685227G=CA2229889212CDH3c.1447G= (p.Ala483=)
c.*1185G= (n.*1185G=)
c.1282G= (p.Ala428=)
16g.68685227G>TCA396454289CDH3c.1447G>T (p.Ala483Ser)
c.*1185G>T (n.*1185G>T)
c.1282G>T (p.Ala428Ser)
16g.68685228C>ACA396454291CDH3c.1448C>A (p.Ala483Glu)
c.*1186C>A (n.*1186C>A)
c.1283C>A (p.Ala428Glu)
16g.68685228C>GCA396454292CDH3c.1448C>G (p.Ala483Gly)
c.*1186C>G (n.*1186C>G)
c.1283C>G (p.Ala428Gly)
16g.68685228C>TCA396454290CDH3c.1448C>T (p.Ala483Val)
c.*1186C>T (n.*1186C>T)
c.1283C>T (p.Ala428Val)
16g.68685229A=CA2229889213CDH3c.1449A= (p.Ala483=)
c.*1187A= (n.*1187A=)
c.1284A= (p.Ala428=)
16g.68685229A>CCA496154451CDH3c.1449A>C (p.Ala483=)
c.*1187A>C (n.*1187A>C)
c.1284A>C (p.Ala428=)
16g.68685229A>GCA496154452CDH3c.1449A>G (p.Ala483=)
c.*1187A>G (n.*1187A>G)
c.1284A>G (p.Ala428=)
16g.68685229A>TCA496154450CDH3c.1449A>T (p.Ala483=)
c.*1187A>T (n.*1187A>T)
c.1284A>T (p.Ala428=)
 dbSNP
16g.68685230G>ACA396454294CDH3c.1450G>A (p.Gly484Arg)
c.*1188G>A (n.*1188G>A)
c.1285G>A (p.Gly429Arg)
 gnomAD v4
16g.68685230G>CCA396454293CDH3c.1450G>C (p.Gly484Arg)
c.*1188G>C (n.*1188G>C)
c.1285G>C (p.Gly429Arg)
16g.68685230G>TCA396454295CDH3c.1450G>T (p.Gly484Trp)
c.*1188G>T (n.*1188G>T)
c.1285G>T (p.Gly429Trp)
16g.68685231G>ACA396454296CDH3c.1451G>A (p.Gly484Glu)
c.*1189G>A (n.*1189G>A)
c.1286G>A (p.Gly429Glu)
16g.68685231G>CCA396454297CDH3c.1451G>C (p.Gly484Ala)
c.*1189G>C (n.*1189G>C)
c.1286G>C (p.Gly429Ala)
16g.68685231G>TCA396454298CDH3c.1451G>T (p.Gly484Val)
c.*1189G>T (n.*1189G>T)
c.1286G>T (p.Gly429Val)
16g.68685232G>ACA496154455CDH3c.1452G>A (p.Gly484=)
c.*1190G>A (n.*1190G>A)
c.1287G>A (p.Gly429=)
16g.68685232G>CCA496154453CDH3c.1452G>C (p.Gly484=)
c.*1190G>C (n.*1190G>C)
c.1287G>C (p.Gly429=)
16g.68685232G>TCA496154454CDH3c.1452G>T (p.Gly484=)
c.*1190G>T (n.*1190G>T)
c.1287G>T (p.Gly429=)
16g.68685233T>ACA396454299CDH3c.1453T>A (p.Trp485Arg)
c.*1191T>A (n.*1191T>A)
c.1288T>A (p.Trp430Arg)
16g.68685233T>CCA396454300CDH3c.1453T>C (p.Trp485Arg)
c.*1191T>C (n.*1191T>C)
c.1288T>C (p.Trp430Arg)
 gnomAD v4
16g.68685233T>GCA396454301CDH3c.1453T>G (p.Trp485Gly)
c.*1191T>G (n.*1191T>G)
c.1288T>G (p.Trp430Gly)
16g.68685234G>ACA396454302CDH3c.1454G>A (p.Trp485Ter)
c.*1192G>A (n.*1192G>A)
c.1289G>A (p.Trp430Ter)
16g.68685234G>CCA396454303CDH3c.1454G>C (p.Trp485Ser)
c.*1192G>C (n.*1192G>C)
c.1289G>C (p.Trp430Ser)
16g.68685234G>TCA396454304CDH3c.1454G>T (p.Trp485Leu)
c.*1192G>T (n.*1192G>T)
c.1289G>T (p.Trp430Leu)
16g.68685235G>ACA396454305CDH3c.1455G>A (p.Trp485Ter)
c.*1193G>A (n.*1193G>A)
c.1290G>A (p.Trp430Ter)
16g.68685235G>CCA396454306CDH3c.1455G>C (p.Trp485Cys)
c.*1193G>C (n.*1193G>C)
c.1290G>C (p.Trp430Cys)
16g.68685235G=CA2229889214CDH3c.1455G= (p.Trp485=)
c.*1193G= (n.*1193G=)
c.1290G= (p.Trp430=)
16g.68685235G>TCA396454307CDH3c.1455G>T (p.Trp485Cys)
c.*1193G>T (n.*1193G>T)
c.1290G>T (p.Trp430Cys)
 dbSNP gnomAD v2
16g.68685236C>ACA8129367CDH3c.1456C>A (p.Leu486Ile)
c.*1194C>A (n.*1194C>A)
c.1291C>A (p.Leu431Ile)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.68685236C=CA2229889215CDH3c.1456C= (p.Leu486=)
c.*1194C= (n.*1194C=)
c.1291C= (p.Leu431=)
16g.68685236C>GCA396454308CDH3c.1456C>G (p.Leu486Val)
c.*1194C>G (n.*1194C>G)
c.1291C>G (p.Leu431Val)
16g.68685236C>TCA496154456CDH3c.1456C>T (p.Leu486=)
c.*1194C>T (n.*1194C>T)
c.1291C>T (p.Leu431=)
 gnomAD v4
16g.68685237T>ACA396454309CDH3c.1457T>A (p.Leu486Gln)
c.*1195T>A (n.*1195T>A)
c.1292T>A (p.Leu431Gln)
16g.68685237T>CCA396454310CDH3c.1457T>C (p.Leu486Pro)
c.*1195T>C (n.*1195T>C)
c.1292T>C (p.Leu431Pro)
16g.68685237T>GCA396454311CDH3c.1457T>G (p.Leu486Arg)
c.*1195T>G (n.*1195T>G)
c.1292T>G (p.Leu431Arg)
16g.68685238A>CCA496154459CDH3c.1458A>C (p.Leu486=)
c.*1196A>C (n.*1196A>C)
c.1293A>C (p.Leu431=)
16g.68685238A>GCA496154458CDH3c.1458A>G (p.Leu486=)
c.*1196A>G (n.*1196A>G)
c.1293A>G (p.Leu431=)
16g.68685238A>TCA496154457CDH3c.1458A>T (p.Leu486=)
c.*1196A>T (n.*1196A>T)
c.1293A>T (p.Leu431=)
16g.68685239G>ACA396454312CDH3c.1459G>A (p.Ala487Thr)
c.*1197G>A (n.*1197G>A)
c.1294G>A (p.Ala432Thr)
 gnomAD v4
16g.68685239G>CCA396454313CDH3c.1459G>C (p.Ala487Pro)
c.*1197G>C (n.*1197G>C)
c.1294G>C (p.Ala432Pro)
16g.68685239G>TCA396454314CDH3c.1459G>T (p.Ala487Ser)
c.*1197G>T (n.*1197G>T)
c.1294G>T (p.Ala432Ser)
16g.68685240C>ACA396454315CDH3c.1460C>A (p.Ala487Asp)
c.*1198C>A (n.*1198C>A)
c.1295C>A (p.Ala432Asp)
16g.68685240C>GCA396454316CDH3c.1460C>G (p.Ala487Gly)
c.*1198C>G (n.*1198C>G)
c.1295C>G (p.Ala432Gly)
16g.68685240C>TCA396454317CDH3c.1460C>T (p.Ala487Val)
c.*1198C>T (n.*1198C>T)
c.1295C>T (p.Ala432Val)
16g.68685241C>ACA496154462CDH3c.1461C>A (p.Ala487=)
c.*1199C>A (n.*1199C>A)
c.1296C>A (p.Ala432=)
16g.68685241C>GCA496154460CDH3c.1461C>G (p.Ala487=)
c.*1199C>G (n.*1199C>G)
c.1296C>G (p.Ala432=)
16g.68685241C>TCA496154461CDH3c.1461C>T (p.Ala487=)
c.*1199C>T (n.*1199C>T)
c.1296C>T (p.Ala432=)
 gnomAD v4
16g.68685242A=CA2229889216CDH3c.1462A= (p.Met488=)
c.*1200A= (n.*1200A=)
c.1297A= (p.Met433=)
16g.68685242A>CCA396454318CDH3c.1462A>C (p.Met488Leu)
c.*1200A>C (n.*1200A>C)
c.1297A>C (p.Met433Leu)
16g.68685242A>GCA8129368CDH3c.1462A>G (p.Met488Val)
c.*1200A>G (n.*1200A>G)
c.1297A>G (p.Met433Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.68685242A>TCA396454319CDH3c.1462A>T (p.Met488Leu)
c.*1200A>T (n.*1200A>T)
c.1297A>T (p.Met433Leu)
16g.68685243T>ACA396454321CDH3c.1463T>A (p.Met488Lys)
c.*1201T>A (n.*1201T>A)
c.1298T>A (p.Met433Lys)
16g.68685243T>CCA396454322CDH3c.1463T>C (p.Met488Thr)
c.*1201T>C (n.*1201T>C)
c.1298T>C (p.Met433Thr)
 dbSNP
16g.68685243T>GCA396454320CDH3c.1463T>G (p.Met488Arg)
c.*1201T>G (n.*1201T>G)
c.1298T>G (p.Met433Arg)
16g.68685243T=CA2229889217CDH3c.1463T= (p.Met488=)
c.*1201T= (n.*1201T=)
c.1298T= (p.Met433=)
16g.68685244G>ACA396454323CDH3c.1464G>A (p.Met488Ile)
c.*1202G>A (n.*1202G>A)
c.1299G>A (p.Met433Ile)
16g.68685244G>CCA396454324CDH3c.1464G>C (p.Met488Ile)
c.*1202G>C (n.*1202G>C)
c.1299G>C (p.Met433Ile)
16g.68685244G>TCA396454325CDH3c.1464G>T (p.Met488Ile)
c.*1202G>T (n.*1202G>T)
c.1299G>T (p.Met433Ile)
16g.68685245G>ACA396454326CDH3c.1465G>A (p.Asp489Asn)
c.*1203G>A (n.*1203G>A)
c.1300G>A (p.Asp434Asn)
 ClinVar gnomAD v4
16g.68685245G>CCA396454327CDH3c.1465G>C (p.Asp489His)
c.*1203G>C (n.*1203G>C)
c.1300G>C (p.Asp434His)
16g.68685245G>TCA396454328CDH3c.1465G>T (p.Asp489Tyr)
c.*1203G>T (n.*1203G>T)
c.1300G>T (p.Asp434Tyr)
16g.68685246A=CA2229889218CDH3c.1466A= (p.Asp489=)
c.*1204A= (n.*1204A=)
c.1301A= (p.Asp434=)
16g.68685246A>CCA396454329CDH3c.1466A>C (p.Asp489Ala)
c.*1204A>C (n.*1204A>C)
c.1301A>C (p.Asp434Ala)
16g.68685246A>GCA8129369CDH3c.1466A>G (p.Asp489Gly)
c.*1204A>G (n.*1204A>G)
c.1301A>G (p.Asp434Gly)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.68685246A>TCA396454330CDH3c.1466A>T (p.Asp489Val)
c.*1204A>T (n.*1204A>T)
c.1301A>T (p.Asp434Val)
16g.68685247C>ACA396454331CDH3c.1467C>A (p.Asp489Glu)
c.*1205C>A (n.*1205C>A)
c.1302C>A (p.Asp434Glu)
 gnomAD v4
16g.68685247C=CA2229889219CDH3c.1467C= (p.Asp489=)
c.*1205C= (n.*1205C=)
c.1302C= (p.Asp434=)
16g.68685247C>GCA396454332CDH3c.1467C>G (p.Asp489Glu)
c.*1205C>G (n.*1205C>G)
c.1302C>G (p.Asp434Glu)
16g.68685247C>TCA8129370CDH3c.1467C>T (p.Asp489=)
c.*1205C>T (n.*1205C>T)
c.1302C>T (p.Asp434=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.68685248C>ACA396454334CDH3c.1468C>A (p.Pro490Thr)
c.*1206C>A (n.*1206C>A)
c.1303C>A (p.Pro435Thr)
16g.68685248C>GCA396454335CDH3c.1468C>G (p.Pro490Ala)
c.*1206C>G (n.*1206C>G)
c.1303C>G (p.Pro435Ala)
16g.68685248C>TCA396454333CDH3c.1468C>T (p.Pro490Ser)
c.*1206C>T (n.*1206C>T)
c.1303C>T (p.Pro435Ser)
16g.68685249C>ACA396454336CDH3c.1469C>A (p.Pro490Gln)
c.*1207C>A (n.*1207C>A)
c.1304C>A (p.Pro435Gln)
16g.68685249C>GCA396454337CDH3c.1469C>G (p.Pro490Arg)
c.*1207C>G (n.*1207C>G)
c.1304C>G (p.Pro435Arg)
 dbSNP gnomAD v3 gnomAD v4
16g.68685249C>TCA396454338CDH3c.1469C>T (p.Pro490Leu)
c.*1207C>T (n.*1207C>T)
c.1304C>T (p.Pro435Leu)
16g.68685252_68685255delCA2739290827CDH3c.1472_1475del (p.Asp491ValfsTer18)
c.*1210_*1213del (n.*1210_*1213del)
c.1307_1310del (p.Asp436ValfsTer18)
16g.68685250A>CCA496154463CDH3c.1470A>C (p.Pro490=)
c.*1208A>C (n.*1208A>C)
c.1305A>C (p.Pro435=)
16g.68685250A>GCA496154464CDH3c.1470A>G (p.Pro490=)
c.*1208A>G (n.*1208A>G)
c.1305A>G (p.Pro435=)
16g.68685250A>TCA496154465CDH3c.1470A>T (p.Pro490=)
c.*1208A>T (n.*1208A>T)
c.1305A>T (p.Pro435=)
16g.68685251G>ACA396454339CDH3c.1471G>A (p.Asp491Asn)
c.*1209G>A (n.*1209G>A)
c.1306G>A (p.Asp436Asn)
16g.68685251G>CCA396454340CDH3c.1471G>C (p.Asp491His)
c.*1209G>C (n.*1209G>C)
c.1306G>C (p.Asp436His)
 gnomAD v4
16g.68685251G>TCA396454341CDH3c.1471G>T (p.Asp491Tyr)
c.*1209G>T (n.*1209G>T)
c.1306G>T (p.Asp436Tyr)
16g.68685252A>CCA396454344CDH3c.1472A>C (p.Asp491Ala)
c.*1210A>C (n.*1210A>C)
c.1307A>C (p.Asp436Ala)
16g.68685252A>GCA396454342CDH3c.1472A>G (p.Asp491Gly)
c.*1210A>G (n.*1210A>G)
c.1307A>G (p.Asp436Gly)
 dbSNP
16g.68685252A>TCA396454343CDH3c.1472A>T (p.Asp491Val)
c.*1210A>T (n.*1210A>T)
c.1307A>T (p.Asp436Val)
16g.68685253C>ACA396454345CDH3c.1473C>A (p.Asp491Glu)
c.*1211C>A (n.*1211C>A)
c.1308C>A (p.Asp436Glu)
16g.68685253C=CA2229889220CDH3c.1473C= (p.Asp491=)
c.*1211C= (n.*1211C=)
c.1308C= (p.Asp436=)
16g.68685253C>GCA396454346CDH3c.1473C>G (p.Asp491Glu)
c.*1211C>G (n.*1211C>G)
c.1308C>G (p.Asp436Glu)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.68685253C>TCA496154466CDH3c.1473C>T (p.Asp491=)
c.*1211C>T (n.*1211C>T)
c.1308C>T (p.Asp436=)
 gnomAD v4
16g.68685254A=CA2229889221CDH3c.1474A= (p.Ser492=)
c.*1212A= (n.*1212A=)
c.1309A= (p.Ser437=)
16g.68685254A>CCA396454347CDH3c.1474A>C (p.Ser492Arg)
c.*1212A>C (n.*1212A>C)
c.1309A>C (p.Ser437Arg)
16g.68685254A>GCA8129371CDH3c.1474A>G (p.Ser492Gly)
c.*1212A>G (n.*1212A>G)
c.1309A>G (p.Ser437Gly)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.68685254A>TCA396454348CDH3c.1474A>T (p.Ser492Cys)
c.*1212A>T (n.*1212A>T)
c.1309A>T (p.Ser437Cys)
16g.68685255G>ACA396454351CDH3c.1475G>A (p.Ser492Asn)
c.*1213G>A (n.*1213G>A)
c.1310G>A (p.Ser437Asn)
 dbSNP
16g.68685255G>CCA396454350CDH3c.1475G>C (p.Ser492Thr)
c.*1213G>C (n.*1213G>C)
c.1310G>C (p.Ser437Thr)
 dbSNP gnomAD v4
16g.68685255G=CA2229889224CDH3c.1475G= (p.Ser492=)
c.*1213G= (n.*1213G=)
c.1310G= (p.Ser437=)
16g.68685255G>TCA396454349CDH3c.1475G>T (p.Ser492Ile)
c.*1213G>T (n.*1213G>T)
c.1310G>T (p.Ser437Ile)
16g.68685256T>ACA396454352CDH3c.1476T>A (p.Ser492Arg)
c.*1214T>A (n.*1214T>A)
c.1311T>A (p.Ser437Arg)
16g.68685256T>CCA496154467CDH3c.1476T>C (p.Ser492=)
c.*1214T>C (n.*1214T>C)
c.1311T>C (p.Ser437=)
16g.68685256T>GCA396454353CDH3c.1476T>G (p.Ser492Arg)
c.*1214T>G (n.*1214T>G)
c.1311T>G (p.Ser437Arg)
16g.68685257G>ACA396454354CDH3c.1477G>A (p.Gly493Arg)
c.*1215G>A (n.*1215G>A)
c.1312G>A (p.Gly438Arg)
16g.68685257G>CCA396454355CDH3c.1477G>C (p.Gly493Arg)
c.*1215G>C (n.*1215G>C)
c.1312G>C (p.Gly438Arg)
16g.68685257G>TCA396454356CDH3c.1477G>T (p.Gly493Trp)
c.*1215G>T (n.*1215G>T)
c.1312G>T (p.Gly438Trp)
16g.68685258G>ACA8129372CDH3c.1478G>A (p.Gly493Glu)
c.*1216G>A (n.*1216G>A)
c.1313G>A (p.Gly438Glu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.68685258G>CCA396454357CDH3c.1478G>C (p.Gly493Ala)
c.*1216G>C (n.*1216G>C)
c.1313G>C (p.Gly438Ala)
16g.68685258G=CA2229889228CDH3c.1478G= (p.Gly493=)
c.*1216G= (n.*1216G=)
c.1313G= (p.Gly438=)
16g.68685258G>TCA396454358CDH3c.1478G>T (p.Gly493Val)
c.*1216G>T (n.*1216G>T)
c.1313G>T (p.Gly438Val)
 ClinVar
16g.68685259G>ACA8129373CDH3c.1479G>A (p.Gly493=)
c.*1217G>A (n.*1217G>A)
c.1314G>A (p.Gly438=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.68685259G>CCA496154468CDH3c.1479G>C (p.Gly493=)
c.*1217G>C (n.*1217G>C)
c.1314G>C (p.Gly438=)
16g.68685259G=CA2229889232CDH3c.1479G= (p.Gly493=)
c.*1217G= (n.*1217G=)
c.1314G= (p.Gly438=)
16g.68685259G>TCA496154469CDH3c.1479G>T (p.Gly493=)
c.*1217G>T (n.*1217G>T)
c.1314G>T (p.Gly438=)
16g.68685260C>ACA396454359CDH3c.1480C>A (p.Gln494Lys)
c.*1218C>A (n.*1218C>A)
c.1315C>A (p.Gln439Lys)
16g.68685260C>GCA396454360CDH3c.1480C>G (p.Gln494Glu)
c.*1218C>G (n.*1218C>G)
c.1315C>G (p.Gln439Glu)
 gnomAD v4
16g.68685260C>TCA396454361CDH3c.1480C>T (p.Gln494Ter)
c.*1218C>T (n.*1218C>T)
c.1315C>T (p.Gln439Ter)
16g.68685261A=CA2229889235CDH3c.1481A= (p.Gln494=)
c.*1219A= (n.*1219A=)
c.1316A= (p.Gln439=)
16g.68685261A>CCA396454362CDH3c.1481A>C (p.Gln494Pro)
c.*1219A>C (n.*1219A>C)
c.1316A>C (p.Gln439Pro)
16g.68685261A>GCA8129374CDH3c.1481A>G (p.Gln494Arg)
c.*1219A>G (n.*1219A>G)
c.1316A>G (p.Gln439Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.68685261A>TCA396454363CDH3c.1481A>T (p.Gln494Leu)
c.*1219A>T (n.*1219A>T)
c.1316A>T (p.Gln439Leu)
16g.68685262G>ACA496154470CDH3c.1482G>A (p.Gln494=)
c.*1220G>A (n.*1220G>A)
c.1317G>A (p.Gln439=)
16g.68685262G>CCA396454365CDH3c.1482G>C (p.Gln494His)
c.*1220G>C (n.*1220G>C)
c.1317G>C (p.Gln439His)
16g.68685262G>TCA396454364CDH3c.1482G>T (p.Gln494His)
c.*1220G>T (n.*1220G>T)
c.1317G>T (p.Gln439His)
16g.68685263G>ACA396454366CDH3c.1483G>A (p.Val495Ile)
c.*1221G>A (n.*1221G>A)
c.1318G>A (p.Val440Ile)
 dbSNP gnomAD v2 gnomAD v4
16g.68685263G>CCA396454367CDH3c.1483G>C (p.Val495Leu)
c.*1221G>C (n.*1221G>C)
c.1318G>C (p.Val440Leu)
16g.68685263G=CA2229889237CDH3c.1483G= (p.Val495=)
c.*1221G= (n.*1221G=)
c.1318G= (p.Val440=)
16g.68685263G>TCA396454368CDH3c.1483G>T (p.Val495Phe)
c.*1221G>T (n.*1221G>T)
c.1318G>T (p.Val440Phe)
 ClinVar dbSNP
16g.68685264T>ACA396454369CDH3c.1484T>A (p.Val495Asp)
c.*1222T>A (n.*1222T>A)
c.1319T>A (p.Val440Asp)
16g.68685264T>CCA396454370CDH3c.1484T>C (p.Val495Ala)
c.*1222T>C (n.*1222T>C)
c.1319T>C (p.Val440Ala)
16g.68685264T>GCA396454371CDH3c.1484T>G (p.Val495Gly)
c.*1222T>G (n.*1222T>G)
c.1319T>G (p.Val440Gly)
16g.68685265C>ACA496154471CDH3c.1485C>A (p.Val495=)
c.*1223C>A (n.*1223C>A)
c.1320C>A (p.Val440=)
16g.68685265C>GCA496154472CDH3c.1485C>G (p.Val495=)
c.*1223C>G (n.*1223C>G)
c.1320C>G (p.Val440=)
16g.68685265C>TCA496154473CDH3c.1485C>T (p.Val495=)
c.*1223C>T (n.*1223C>T)
c.1320C>T (p.Val440=)
 gnomAD v4
16g.68685266A>CCA396454372CDH3c.1486A>C (p.Thr496Pro)
c.*1224A>C (n.*1224A>C)
c.1321A>C (p.Thr441Pro)
16g.68685266A>GCA396454373CDH3c.1486A>G (p.Thr496Ala)
c.*1224A>G (n.*1224A>G)
c.1321A>G (p.Thr441Ala)
16g.68685266A>TCA396454374CDH3c.1486A>T (p.Thr496Ser)
c.*1224A>T (n.*1224A>T)
c.1321A>T (p.Thr441Ser)
16g.68685267C>ACA396454375CDH3c.1487C>A (p.Thr496Lys)
c.*1225C>A (n.*1225C>A)
c.1322C>A (p.Thr441Lys)
16g.68685267C>GCA396454376CDH3c.1487C>G (p.Thr496Arg)
c.*1225C>G (n.*1225C>G)
c.1322C>G (p.Thr441Arg)
16g.68685267C>TCA396454377CDH3c.1487C>T (p.Thr496Ile)
c.*1225C>T (n.*1225C>T)
c.1322C>T (p.Thr441Ile)
 gnomAD v4
16g.68685268A>CCA496154474CDH3c.1488A>C (p.Thr496=)
c.*1226A>C (n.*1226A>C)
c.1323A>C (p.Thr441=)
16g.68685268A>GCA496154475CDH3c.1488A>G (p.Thr496=)
c.*1226A>G (n.*1226A>G)
c.1323A>G (p.Thr441=)
16g.68685268A>TCA496154476CDH3c.1488A>T (p.Thr496=)
c.*1226A>T (n.*1226A>T)
c.1323A>T (p.Thr441=)
16g.68685269G>ACA396454380CDH3c.1489G>A (p.Ala497Thr)
c.*1227G>A (n.*1227G>A)
c.1324G>A (p.Ala442Thr)
 gnomAD v4
16g.68685269G>CCA396454379CDH3c.1489G>C (p.Ala497Pro)
c.*1227G>C (n.*1227G>C)
c.1324G>C (p.Ala442Pro)
16g.68685269G>TCA396454378CDH3c.1489G>T (p.Ala497Ser)
c.*1227G>T (n.*1227G>T)
c.1324G>T (p.Ala442Ser)
16g.68685270C>ACA396454381CDH3c.1490C>A (p.Ala497Asp)
c.*1228C>A (n.*1228C>A)
c.1325C>A (p.Ala442Asp)
16g.68685270C>GCA396454382CDH3c.1490C>G (p.Ala497Gly)
c.*1228C>G (n.*1228C>G)
c.1325C>G (p.Ala442Gly)
16g.68685270C>TCA396454383CDH3c.1490C>T (p.Ala497Val)
c.*1228C>T (n.*1228C>T)
c.1325C>T (p.Ala442Val)
16g.68685271T>ACA496154477CDH3c.1491T>A (p.Ala497=)
c.*1229T>A (n.*1229T>A)
c.1326T>A (p.Ala442=)
16g.68685271T>CCA496154478CDH3c.1491T>C (p.Ala497=)
c.*1229T>C (n.*1229T>C)
c.1326T>C (p.Ala442=)
 gnomAD v4
16g.68685271T>GCA496154479CDH3c.1491T>G (p.Ala497=)
c.*1229T>G (n.*1229T>G)
c.1326T>G (p.Ala442=)
16g.68685272G>ACA8129376CDH3c.1492G>A (p.Val498Met)
c.*1230G>A (n.*1230G>A)
c.1327G>A (p.Val443Met)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.68685272G>CCA8129375CDH3c.1492G>C (p.Val498Leu)
c.*1230G>C (n.*1230G>C)
c.1327G>C (p.Val443Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
16g.68685272G=CA2229889239CDH3c.1492G= (p.Val498=)
c.*1230G= (n.*1230G=)
c.1327G= (p.Val443=)
16g.68685272G>TCA396454384CDH3c.1492G>T (p.Val498Leu)
c.*1230G>T (n.*1230G>T)
c.1327G>T (p.Val443Leu)
16g.68685273T>ACA396454385CDH3c.1493T>A (p.Val498Glu)
c.*1231T>A (n.*1231T>A)
c.1328T>A (p.Val443Glu)
16g.68685273T>CCA396454386CDH3c.1493T>C (p.Val498Ala)
c.*1231T>C (n.*1231T>C)
c.1328T>C (p.Val443Ala)
16g.68685273T>GCA396454387CDH3c.1493T>G (p.Val498Gly)
c.*1231T>G (n.*1231T>G)
c.1328T>G (p.Val443Gly)
 gnomAD v4
16g.68685274G>ACA496154480CDH3c.1494G>A (p.Val498=)
c.*1232G>A (n.*1232G>A)
c.1329G>A (p.Val443=)
 gnomAD v4
16g.68685274G>CCA496154481CDH3c.1494G>C (p.Val498=)
c.*1232G>C (n.*1232G>C)
c.1329G>C (p.Val443=)
16g.68685274G>TCA496154482CDH3c.1494G>T (p.Val498=)
c.*1232G>T (n.*1232G>T)
c.1329G>T (p.Val443=)
16g.68685275G>ACA396454388CDH3c.1495G>A (p.Gly499Ser)
c.*1233G>A (n.*1233G>A)
c.1330G>A (p.Gly444Ser)
 gnomAD v4
16g.68685275G>CCA396454389CDH3c.1495G>C (p.Gly499Arg)
c.*1233G>C (n.*1233G>C)
c.1330G>C (p.Gly444Arg)
16g.68685275G>TCA396454390CDH3c.1495G>T (p.Gly499Cys)
c.*1233G>T (n.*1233G>T)
c.1330G>T (p.Gly444Cys)
16g.68685276G>ACA396454392CDH3c.1496G>A (p.Gly499Asp)
c.*1234G>A (n.*1234G>A)
c.1331G>A (p.Gly444Asp)
16g.68685276G>CCA396454393CDH3c.1496G>C (p.Gly499Ala)
c.*1234G>C (n.*1234G>C)
c.1331G>C (p.Gly444Ala)
16g.68685276G>TCA396454391CDH3c.1496G>T (p.Gly499Val)
c.*1234G>T (n.*1234G>T)
c.1331G>T (p.Gly444Val)
16g.68685277C>ACA8129377CDH3c.1497C>A (p.Gly499=)
c.*1235C>A (n.*1235C>A)
c.1332C>A (p.Gly444=)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.68685277C=CA2229889242CDH3c.1497C= (p.Gly499=)
c.*1235C= (n.*1235C=)
c.1332C= (p.Gly444=)
16g.68685277C>GCA496154483CDH3c.1497C>G (p.Gly499=)
c.*1235C>G (n.*1235C>G)
c.1332C>G (p.Gly444=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
16g.68685277C>TCA496154484CDH3c.1497C>T (p.Gly499=)
c.*1235C>T (n.*1235C>T)
c.1332C>T (p.Gly444=)
16g.68685278A>CCA396454394CDH3c.1498A>C (p.Thr500Pro)
c.*1236A>C (n.*1236A>C)
c.1333A>C (p.Thr445Pro)
16g.68685278A>GCA396454395CDH3c.1498A>G (p.Thr500Ala)
c.*1236A>G (n.*1236A>G)
c.1333A>G (p.Thr445Ala)
 gnomAD v4
16g.68685278A>TCA396454396CDH3c.1498A>T (p.Thr500Ser)
c.*1236A>T (n.*1236A>T)
c.1333A>T (p.Thr445Ser)
16g.68685279C>ACA396454399CDH3c.1499C>A (p.Thr500Asn)
c.*1237C>A (n.*1237C>A)
c.1334C>A (p.Thr445Asn)
16g.68685279C=CA2229889247CDH3c.1499C= (p.Thr500=)
c.*1237C= (n.*1237C=)
c.1334C= (p.Thr445=)
16g.68685279C>GCA396454398CDH3c.1499C>G (p.Thr500Ser)
c.*1237C>G (n.*1237C>G)
c.1334C>G (p.Thr445Ser)
16g.68685279C>TCA396454397CDH3c.1499C>T (p.Thr500Ile)
c.*1237C>T (n.*1237C>T)
c.1334C>T (p.Thr445Ile)
 dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC
16g.68685280C>ACA283280908CDH3c.1500C>A (p.Thr500=)
c.*1238C>A (n.*1238C>A)
c.1335C>A (p.Thr445=)
 dbSNP
16g.68685280C=CA2229889251CDH3c.1500C= (p.Thr500=)
c.*1238C= (n.*1238C=)
c.1335C= (p.Thr445=)
16g.68685280C>GCA496154485CDH3c.1500C>G (p.Thr500=)
c.*1238C>G (n.*1238C>G)
c.1335C>G (p.Thr445=)
16g.68685280C>TCA8129378CDH3c.1500C>T (p.Thr500=)
c.*1238C>T (n.*1238C>T)
c.1335C>T (p.Thr445=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.68685281C>ACA396454400CDH3c.1501C>A (p.Leu501Ile)
c.*1239C>A (n.*1239C>A)
c.1336C>A (p.Leu446Ile)
16g.68685281C=CA2229889258CDH3c.1501C= (p.Leu501=)
c.*1239C= (n.*1239C=)
c.1336C= (p.Leu446=)
16g.68685281C>GCA396454401CDH3c.1501C>G (p.Leu501Val)
c.*1239C>G (n.*1239C>G)
c.1336C>G (p.Leu446Val)
 dbSNP gnomAD v4
16g.68685281C>TCA396454402CDH3c.1501C>T (p.Leu501Phe)
c.*1239C>T (n.*1239C>T)
c.1336C>T (p.Leu446Phe)
 dbSNP
16g.68685282T>ACA396454403CDH3c.1502T>A (p.Leu501His)
c.*1240T>A (n.*1240T>A)
c.1337T>A (p.Leu446His)
16g.68685282T>CCA396454404CDH3c.1502T>C (p.Leu501Pro)
c.*1240T>C (n.*1240T>C)
c.1337T>C (p.Leu446Pro)
16g.68685282T>GCA396454405CDH3c.1502T>G (p.Leu501Arg)
c.*1240T>G (n.*1240T>G)
c.1337T>G (p.Leu446Arg)
16g.68685283C>ACA496154486CDH3c.1503C>A (p.Leu501=)
c.*1241C>A (n.*1241C>A)
c.1338C>A (p.Leu446=)
16g.68685283C=CA2229889260CDH3c.1503C= (p.Leu501=)
c.*1241C= (n.*1241C=)
c.1338C= (p.Leu446=)
16g.68685283C>GCA8129379CDH3c.1503C>G (p.Leu501=)
c.*1241C>G (n.*1241C>G)
c.1338C>G (p.Leu446=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.68685283C>TCA8129380CDH3c.1503C>T (p.Leu501=)
c.*1241C>T (n.*1241C>T)
c.1338C>T (p.Leu446=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.68685284G>ACA8129381CDH3c.1504G>A (p.Asp502Asn)
c.*1242G>A (n.*1242G>A)
c.1339G>A (p.Asp447Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
16g.68685284G>CCA396454407CDH3c.1504G>C (p.Asp502His)
c.*1242G>C (n.*1242G>C)
c.1339G>C (p.Asp447His)
16g.68685284G=CA2229889264CDH3c.1504G= (p.Asp502=)
c.*1242G= (n.*1242G=)
c.1339G= (p.Asp447=)
16g.68685284G>TCA396454406CDH3c.1504G>T (p.Asp502Tyr)
c.*1242G>T (n.*1242G>T)
c.1339G>T (p.Asp447Tyr)
16g.68685285A>CCA396454408CDH3c.1505A>C (p.Asp502Ala)
c.*1243A>C (n.*1243A>C)
c.1340A>C (p.Asp447Ala)
16g.68685285A>GCA396454410CDH3c.1505A>G (p.Asp502Gly)
c.*1243A>G (n.*1243A>G)
c.1340A>G (p.Asp447Gly)
 COSMIC COSMIC
16g.68685285A>TCA396454409CDH3c.1505A>T (p.Asp502Val)
c.*1243A>T (n.*1243A>T)
c.1340A>T (p.Asp447Val)
16g.68685286C>ACA396454411CDH3c.1506C>A (p.Asp502Glu)
c.*1244C>A (n.*1244C>A)
c.1341C>A (p.Asp447Glu)
16g.68685286C>GCA396454412CDH3c.1506C>G (p.Asp502Glu)
c.*1244C>G (n.*1244C>G)
c.1341C>G (p.Asp447Glu)
16g.68685286C>TCA496154487CDH3c.1506C>T (p.Asp502=)
c.*1244C>T (n.*1244C>T)
c.1341C>T (p.Asp447=)
 ClinVar
16g.68685287C>ACA396454413CDH3c.1507C>A (p.Arg503Ser)
c.*1245C>A (n.*1245C>A)
c.1342C>A (p.Arg448Ser)
16g.68685287C=CA2229889269CDH3c.1507C= (p.Arg503=)
c.*1245C= (n.*1245C=)
c.1342C= (p.Arg448=)
16g.68685287C>GCA396454414CDH3c.1507C>G (p.Arg503Gly)
c.*1245C>G (n.*1245C>G)
c.1342C>G (p.Arg448Gly)
16g.68685287C>TCA8129382CDH3c.1507C>T (p.Arg503Cys)
c.*1245C>T (n.*1245C>T)
c.1342C>T (p.Arg448Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
16g.68685288G>ACA127316CDH3c.1508G>A (p.Arg503His)
c.*1246G>A (n.*1246G>A)
c.1343G>A (p.Arg448His)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.68685288G>CCA396454415CDH3c.1508G>C (p.Arg503Pro)
c.*1246G>C (n.*1246G>C)
c.1343G>C (p.Arg448Pro)
16g.68685288G=CA2229889279CDH3c.1508G= (p.Arg503=)
c.*1246G= (n.*1246G=)
c.1343G= (p.Arg448=)
16g.68685288G>TCA396454416CDH3c.1508G>T (p.Arg503Leu)
c.*1246G>T (n.*1246G>T)
c.1343G>T (p.Arg448Leu)
 gnomAD v4

Number of alleles fetched