Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.211702005C>ACA350442243ERBB4c.1451G>T (p.Arg484Ile)
c.1373G>T (p.Arg458Ile)
c.1450G>T
c.1274G>T (p.Arg425Ile)
n.1503G>T
c.1529G>T (p.Arg510Ile)
c.830G>T (p.Arg277Ile)
2g.211702005C=CA1325614759ERBB4c.1451G= (p.Arg484=)
c.1373G= (p.Arg458=)
c.1450G=
c.1274G= (p.Arg425=)
n.1503G=
c.1529G= (p.Arg510=)
c.830G= (p.Arg277=)
2g.211702005C>GCA350442244ERBB4c.1451G>C (p.Arg484Thr)
c.1373G>C (p.Arg458Thr)
c.1450G>C
c.1274G>C (p.Arg425Thr)
n.1503G>C
c.1529G>C (p.Arg510Thr)
c.830G>C (p.Arg277Thr)
dbSNP gnomAD v2 gnomAD v4
2g.211702005C>TCA64751871ERBB4c.1451G>A (p.Arg484Lys)
c.1373G>A (p.Arg458Lys)
c.1450G>A
c.1274G>A (p.Arg425Lys)
n.1503G>A
c.1529G>A (p.Arg510Lys)
c.830G>A (p.Arg277Lys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
2g.211702006T>ACA350442246ERBB4c.1450A>T (p.Arg484Ter)
c.1372A>T (p.Arg458Ter)
c.1449A>T
c.1273A>T (p.Arg425Ter)
n.1502A>T
c.1528A>T (p.Arg510Ter)
c.829A>T (p.Arg277Ter)
2g.211702006T>CCA350442245ERBB4c.1450A>G (p.Arg484Gly)
c.1372A>G (p.Arg458Gly)
c.1449A>G
c.1273A>G (p.Arg425Gly)
n.1502A>G
c.1528A>G (p.Arg510Gly)
c.829A>G (p.Arg277Gly)
dbSNP
2g.211702006T>GCA431130616ERBB4c.1450A>C (p.Arg484=)
c.1372A>C (p.Arg458=)
c.1449A>C
c.1273A>C (p.Arg425=)
n.1502A>C
c.1528A>C (p.Arg510=)
c.829A>C (p.Arg277=)
2g.211702007C>ACA350442247ERBB4c.1449G>T (p.Gln483His)
c.1371G>T (p.Gln457His)
c.1448G>T
c.1272G>T (p.Gln424His)
n.1501G>T
c.1527G>T (p.Gln509His)
c.828G>T (p.Gln276His)
2g.211702007C>GCA350442248ERBB4c.1449G>C (p.Gln483His)
c.1371G>C (p.Gln457His)
c.1448G>C
c.1272G>C (p.Gln424His)
n.1501G>C
c.1527G>C (p.Gln509His)
c.828G>C (p.Gln276His)
dbSNP
2g.211702007C>TCA431130618ERBB4c.1449G>A (p.Gln483=)
c.1371G>A (p.Gln457=)
c.1448G>A
c.1272G>A (p.Gln424=)
n.1501G>A
c.1527G>A (p.Gln509=)
c.828G>A (p.Gln276=)
dbSNP
2g.211702008T>ACA350442249ERBB4c.1448A>T (p.Gln483Leu)
c.1370A>T (p.Gln457Leu)
c.1447A>T
c.1271A>T (p.Gln424Leu)
n.1500A>T
c.1526A>T (p.Gln509Leu)
c.827A>T (p.Gln276Leu)
2g.211702008T>CCA350442250ERBB4c.1448A>G (p.Gln483Arg)
c.1370A>G (p.Gln457Arg)
c.1447A>G
c.1271A>G (p.Gln424Arg)
n.1500A>G
c.1526A>G (p.Gln509Arg)
c.827A>G (p.Gln276Arg)
gnomAD v4
2g.211702008T>GCA350442251ERBB4c.1448A>C (p.Gln483Pro)
c.1370A>C (p.Gln457Pro)
c.1447A>C
c.1271A>C (p.Gln424Pro)
n.1500A>C
c.1526A>C (p.Gln509Pro)
c.827A>C (p.Gln276Pro)
2g.211702009G>ACA350442252ERBB4c.1447C>T (p.Gln483Ter)
c.1369C>T (p.Gln457Ter)
c.1446C>T
c.1270C>T (p.Gln424Ter)
n.1499C>T
c.1525C>T (p.Gln509Ter)
c.826C>T (p.Gln276Ter)
2g.211702009G>CCA350442253ERBB4c.1447C>G (p.Gln483Glu)
c.1369C>G (p.Gln457Glu)
c.1446C>G
c.1270C>G (p.Gln424Glu)
n.1499C>G
c.1525C>G (p.Gln509Glu)
c.826C>G (p.Gln276Glu)
dbSNP COSMIC
2g.211702009G>TCA350442254ERBB4c.1447C>A (p.Gln483Lys)
c.1369C>A (p.Gln457Lys)
c.1446C>A
c.1270C>A (p.Gln424Lys)
n.1499C>A
c.1525C>A (p.Gln509Lys)
c.826C>A (p.Gln276Lys)
dbSNP
2g.211702010delCA2701479974ERBB4c.1447del (p.Gln483ArgfsTer3)
c.1369del (p.Gln457ArgfsTer3)
c.1446del
c.1270del (p.Gln424ArgfsTer3)
n.1499del
c.1525del (p.Gln509ArgfsTer3)
c.826del (p.Gln276ArgfsTer3)
dbSNP
2g.211702010G>ACA64751872ERBB4c.1446C>T (p.Asn482=)
c.1368C>T (p.Asn456=)
c.1445C>T
c.1269C>T (p.Asn423=)
n.1498C>T
c.1524C>T (p.Asn508=)
c.825C>T (p.Asn275=)
dbSNP gnomAD v2 gnomAD v4
2g.211702010G>CCA350442255ERBB4c.1446C>G (p.Asn482Lys)
c.1368C>G (p.Asn456Lys)
c.1445C>G
c.1269C>G (p.Asn423Lys)
n.1498C>G
c.1524C>G (p.Asn508Lys)
c.825C>G (p.Asn275Lys)
dbSNP
2g.211702010G=CA1325614760ERBB4c.1446C= (p.Asn482=)
c.1368C= (p.Asn456=)
c.1445C=
c.1269C= (p.Asn423=)
n.1498C=
c.1524C= (p.Asn508=)
c.825C= (p.Asn275=)
2g.211702010G>TCA350442256ERBB4c.1446C>A (p.Asn482Lys)
c.1368C>A (p.Asn456Lys)
c.1445C>A
c.1269C>A (p.Asn423Lys)
n.1498C>A
c.1524C>A (p.Asn508Lys)
c.825C>A (p.Asn275Lys)
dbSNP
2g.211702011T>ACA350442257ERBB4c.1445A>T (p.Asn482Ile)
c.1367A>T (p.Asn456Ile)
c.1444A>T
c.1268A>T (p.Asn423Ile)
n.1497A>T
c.1523A>T (p.Asn508Ile)
c.824A>T (p.Asn275Ile)
dbSNP
2g.211702011T>CCA2088132ERBB4c.1445A>G (p.Asn482Ser)
c.1367A>G (p.Asn456Ser)
c.1444A>G
c.1268A>G (p.Asn423Ser)
n.1497A>G
c.1523A>G (p.Asn508Ser)
c.824A>G (p.Asn275Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.211702011T>GCA350442258ERBB4c.1445A>C (p.Asn482Thr)
c.1367A>C (p.Asn456Thr)
c.1444A>C
c.1268A>C (p.Asn423Thr)
n.1497A>C
c.1523A>C (p.Asn508Thr)
c.824A>C (p.Asn275Thr)
2g.211702011T=CA1325614761ERBB4c.1445A= (p.Asn482=)
c.1367A= (p.Asn456=)
c.1444A=
c.1268A= (p.Asn423=)
n.1497A=
c.1523A= (p.Asn508=)
c.824A= (p.Asn275=)
2g.211702012T>ACA350442261ERBB4c.1444A>T (p.Asn482Tyr)
c.1366A>T (p.Asn456Tyr)
c.1443A>T
c.1267A>T (p.Asn423Tyr)
n.1496A>T
c.1522A>T (p.Asn508Tyr)
c.823A>T (p.Asn275Tyr)
2g.211702012T>CCA350442259ERBB4c.1444A>G (p.Asn482Asp)
c.1366A>G (p.Asn456Asp)
c.1443A>G
c.1267A>G (p.Asn423Asp)
n.1496A>G
c.1522A>G (p.Asn508Asp)
c.823A>G (p.Asn275Asp)
2g.211702012T>GCA350442260ERBB4c.1444A>C (p.Asn482His)
c.1366A>C (p.Asn456His)
c.1443A>C
c.1267A>C (p.Asn423His)
n.1496A>C
c.1522A>C (p.Asn508His)
c.823A>C (p.Asn275His)
2g.211702013G>ACA431130653ERBB4c.1443C>T (p.Ile481=)
c.1365C>T (p.Ile455=)
c.1442C>T
c.1266C>T (p.Ile422=)
n.1495C>T
c.1521C>T (p.Ile507=)
c.822C>T (p.Ile274=)
2g.211702013G>CCA350442262ERBB4c.1443C>G (p.Ile481Met)
c.1365C>G (p.Ile455Met)
c.1442C>G
c.1266C>G (p.Ile422Met)
n.1495C>G
c.1521C>G (p.Ile507Met)
c.822C>G (p.Ile274Met)
dbSNP
2g.211702013G>TCA431130654ERBB4c.1443C>A (p.Ile481=)
c.1365C>A (p.Ile455=)
c.1442C>A
c.1266C>A (p.Ile422=)
n.1495C>A
c.1521C>A (p.Ile507=)
c.822C>A (p.Ile274=)
2g.211702014A>CCA350442263ERBB4c.1442T>G (p.Ile481Ser)
c.1364T>G (p.Ile455Ser)
c.1441T>G
c.1265T>G (p.Ile422Ser)
n.1494T>G
c.1520T>G (p.Ile507Ser)
c.821T>G (p.Ile274Ser)
2g.211702014A>GCA350442264ERBB4c.1442T>C (p.Ile481Thr)
c.1364T>C (p.Ile455Thr)
c.1441T>C
c.1265T>C (p.Ile422Thr)
n.1494T>C
c.1520T>C (p.Ile507Thr)
c.821T>C (p.Ile274Thr)
2g.211702014A>TCA350442265ERBB4c.1442T>A (p.Ile481Asn)
c.1364T>A (p.Ile455Asn)
c.1441T>A
c.1265T>A (p.Ile422Asn)
n.1494T>A
c.1520T>A (p.Ile507Asn)
c.821T>A (p.Ile274Asn)
dbSNP
2g.211702015T>ACA350442266ERBB4c.1441A>T (p.Ile481Phe)
c.1363A>T (p.Ile455Phe)
c.1440A>T
c.1264A>T (p.Ile422Phe)
n.1493A>T
c.1519A>T (p.Ile507Phe)
c.820A>T (p.Ile274Phe)
2g.211702015T>CCA2088133ERBB4c.1441A>G (p.Ile481Val)
c.1363A>G (p.Ile455Val)
c.1440A>G
c.1264A>G (p.Ile422Val)
n.1493A>G
c.1519A>G (p.Ile507Val)
c.820A>G (p.Ile274Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.211702015T>GCA350442267ERBB4c.1441A>C (p.Ile481Leu)
c.1363A>C (p.Ile455Leu)
c.1440A>C
c.1264A>C (p.Ile422Leu)
n.1493A>C
c.1519A>C (p.Ile507Leu)
c.820A>C (p.Ile274Leu)
dbSNP
2g.211702015T=CA1325614762ERBB4c.1441A= (p.Ile481=)
c.1363A= (p.Ile455=)
c.1440A=
c.1264A= (p.Ile422=)
n.1493A=
c.1519A= (p.Ile507=)
c.820A= (p.Ile274=)
2g.211702016T>ACA431130684ERBB4c.1440A>T (p.Thr480=)
c.1362A>T (p.Thr454=)
c.1439A>T
c.1263A>T (p.Thr421=)
n.1492A>T
c.1518A>T (p.Thr506=)
c.819A>T (p.Thr273=)
COSMIC
2g.211702016T>CCA431130685ERBB4c.1440A>G (p.Thr480=)
c.1362A>G (p.Thr454=)
c.1439A>G
c.1263A>G (p.Thr421=)
n.1492A>G
c.1518A>G (p.Thr506=)
c.819A>G (p.Thr273=)
gnomAD v4
2g.211702016T>GCA431130687ERBB4c.1440A>C (p.Thr480=)
c.1362A>C (p.Thr454=)
c.1439A>C
c.1263A>C (p.Thr421=)
n.1492A>C
c.1518A>C (p.Thr506=)
c.819A>C (p.Thr273=)
dbSNP gnomAD v3 gnomAD v4
2g.211702016T=CA1325614763ERBB4c.1440A= (p.Thr480=)
c.1362A= (p.Thr454=)
c.1439A=
c.1263A= (p.Thr421=)
n.1492A=
c.1518A= (p.Thr506=)
c.819A= (p.Thr273=)
2g.211702017G>ACA350442268ERBB4c.1439C>T (p.Thr480Ile)
c.1361C>T (p.Thr454Ile)
c.1438C>T
c.1262C>T (p.Thr421Ile)
n.1491C>T
c.1517C>T (p.Thr506Ile)
c.818C>T (p.Thr273Ile)
dbSNP gnomAD v4
2g.211702017G>CCA350442269ERBB4c.1439C>G (p.Thr480Arg)
c.1361C>G (p.Thr454Arg)
c.1438C>G
c.1262C>G (p.Thr421Arg)
n.1491C>G
c.1517C>G (p.Thr506Arg)
c.818C>G (p.Thr273Arg)
dbSNP
2g.211702017G>TCA350442270ERBB4c.1439C>A (p.Thr480Lys)
c.1361C>A (p.Thr454Lys)
c.1438C>A
c.1262C>A (p.Thr421Lys)
n.1491C>A
c.1517C>A (p.Thr506Lys)
c.818C>A (p.Thr273Lys)
2g.211702018T>ACA350442271ERBB4c.1438A>T (p.Thr480Ser)
c.1360A>T (p.Thr454Ser)
c.1437A>T
c.1261A>T (p.Thr421Ser)
n.1490A>T
c.1516A>T (p.Thr506Ser)
c.817A>T (p.Thr273Ser)
dbSNP gnomAD v4
2g.211702018T>CCA350442272ERBB4c.1438A>G (p.Thr480Ala)
c.1360A>G (p.Thr454Ala)
c.1437A>G
c.1261A>G (p.Thr421Ala)
n.1490A>G
c.1516A>G (p.Thr506Ala)
c.817A>G (p.Thr273Ala)
2g.211702018T>GCA350442273ERBB4c.1438A>C (p.Thr480Pro)
c.1360A>C (p.Thr454Pro)
c.1437A>C
c.1261A>C (p.Thr421Pro)
n.1490A>C
c.1516A>C (p.Thr506Pro)
c.817A>C (p.Thr273Pro)
dbSNP
2g.211702019G>ACA431130702ERBB4c.1437C>T (p.Ser479=)
c.1359C>T (p.Ser453=)
c.1436C>T
c.1260C>T (p.Ser420=)
n.1489C>T
c.1515C>T (p.Ser505=)
c.816C>T (p.Ser272=)
dbSNP gnomAD v2 gnomAD v4
2g.211702019G>CCA350442275ERBB4c.1437C>G (p.Ser479Arg)
c.1359C>G (p.Ser453Arg)
c.1436C>G
c.1260C>G (p.Ser420Arg)
n.1489C>G
c.1515C>G (p.Ser505Arg)
c.816C>G (p.Ser272Arg)
dbSNP
2g.211702019G=CA1325614764ERBB4c.1437C= (p.Ser479=)
c.1359C= (p.Ser453=)
c.1436C=
c.1260C= (p.Ser420=)
n.1489C=
c.1515C= (p.Ser505=)
c.816C= (p.Ser272=)
2g.211702019G>TCA350442274ERBB4c.1437C>A (p.Ser479Arg)
c.1359C>A (p.Ser453Arg)
c.1436C>A
c.1260C>A (p.Ser420Arg)
n.1489C>A
c.1515C>A (p.Ser505Arg)
c.816C>A (p.Ser272Arg)
2g.211702020C>ACA350442276ERBB4c.1436G>T (p.Ser479Ile)
c.1358G>T (p.Ser453Ile)
c.1435G>T
c.1259G>T (p.Ser420Ile)
n.1488G>T
c.1514G>T (p.Ser505Ile)
c.815G>T (p.Ser272Ile)
dbSNP
2g.211702020C=CA1325614765ERBB4c.1436G= (p.Ser479=)
c.1358G= (p.Ser453=)
c.1435G=
c.1259G= (p.Ser420=)
n.1488G=
c.1514G= (p.Ser505=)
c.815G= (p.Ser272=)
2g.211702020C>GCA350442277ERBB4c.1436G>C (p.Ser479Thr)
c.1358G>C (p.Ser453Thr)
c.1435G>C
c.1259G>C (p.Ser420Thr)
n.1488G>C
c.1514G>C (p.Ser505Thr)
c.815G>C (p.Ser272Thr)
dbSNP
2g.211702020C>TCA350442278ERBB4c.1436G>A (p.Ser479Asn)
c.1358G>A (p.Ser453Asn)
c.1435G>A
c.1259G>A (p.Ser420Asn)
n.1488G>A
c.1514G>A (p.Ser505Asn)
c.815G>A (p.Ser272Asn)
dbSNP gnomAD v2 gnomAD v4
2g.211702021T>ACA350442279ERBB4c.1435A>T (p.Ser479Cys)
c.1357A>T (p.Ser453Cys)
c.1434A>T
c.1258A>T (p.Ser420Cys)
n.1487A>T
c.1513A>T (p.Ser505Cys)
c.814A>T (p.Ser272Cys)
2g.211702021T>CCA350442280ERBB4c.1435A>G (p.Ser479Gly)
c.1357A>G (p.Ser453Gly)
c.1434A>G
c.1258A>G (p.Ser420Gly)
n.1487A>G
c.1513A>G (p.Ser505Gly)
c.814A>G (p.Ser272Gly)
2g.211702021T>GCA350442281ERBB4c.1435A>C (p.Ser479Arg)
c.1357A>C (p.Ser453Arg)
c.1434A>C
c.1258A>C (p.Ser420Arg)
n.1487A>C
c.1513A>C (p.Ser505Arg)
c.814A>C (p.Ser272Arg)
2g.211702022G>ACA431130711ERBB4c.1434C>T (p.Phe478=)
c.1356C>T (p.Phe452=)
c.1433C>T
c.1257C>T (p.Phe419=)
n.1486C>T
c.1512C>T (p.Phe504=)
c.813C>T (p.Phe271=)
dbSNP
2g.211702022G>CCA350442282ERBB4c.1434C>G (p.Phe478Leu)
c.1356C>G (p.Phe452Leu)
c.1433C>G
c.1257C>G (p.Phe419Leu)
n.1486C>G
c.1512C>G (p.Phe504Leu)
c.813C>G (p.Phe271Leu)
dbSNP
2g.211702022G>TCA350442283ERBB4c.1434C>A (p.Phe478Leu)
c.1356C>A (p.Phe452Leu)
c.1433C>A
c.1257C>A (p.Phe419Leu)
n.1486C>A
c.1512C>A (p.Phe504Leu)
c.813C>A (p.Phe271Leu)
2g.211702023A>CCA350442284ERBB4c.1433T>G (p.Phe478Cys)
c.1355T>G (p.Phe452Cys)
c.1432T>G
c.1256T>G (p.Phe419Cys)
n.1485T>G
c.1511T>G (p.Phe504Cys)
c.812T>G (p.Phe271Cys)
2g.211702023A>GCA350442285ERBB4c.1433T>C (p.Phe478Ser)
c.1355T>C (p.Phe452Ser)
c.1432T>C
c.1256T>C (p.Phe419Ser)
n.1485T>C
c.1511T>C (p.Phe504Ser)
c.812T>C (p.Phe271Ser)
2g.211702023A>TCA350442286ERBB4c.1433T>A (p.Phe478Tyr)
c.1355T>A (p.Phe452Tyr)
c.1432T>A
c.1256T>A (p.Phe419Tyr)
n.1485T>A
c.1511T>A (p.Phe504Tyr)
c.812T>A (p.Phe271Tyr)
dbSNP
2g.211702023_211702025delinsAAGCA1325614766ERBB4c.1431_1433delinsCTT (p.Leu477=)
c.1353_1355delinsCTT (p.Leu451=)
c.1430_1432delinsCTT
c.1254_1256delinsCTT (p.Leu418=)
n.1483_1485delinsCTT
c.1509_1511delinsCTT (p.Leu503=)
c.810_812delinsCTT (p.Leu270=)
2g.211702024A>CCA350442287ERBB4c.1432T>G (p.Phe478Val)
c.1354T>G (p.Phe452Val)
c.1431T>G
c.1255T>G (p.Phe419Val)
n.1484T>G
c.1510T>G (p.Phe504Val)
c.811T>G (p.Phe271Val)
COSMIC
2g.211702024A>GCA350442288ERBB4c.1432T>C (p.Phe478Leu)
c.1354T>C (p.Phe452Leu)
c.1431T>C
c.1255T>C (p.Phe419Leu)
n.1484T>C
c.1510T>C (p.Phe504Leu)
c.811T>C (p.Phe271Leu)
gnomAD v4
2g.211702024A>TCA350442289ERBB4c.1432T>A (p.Phe478Ile)
c.1354T>A (p.Phe452Ile)
c.1431T>A
c.1255T>A (p.Phe419Ile)
n.1484T>A
c.1510T>A (p.Phe504Ile)
c.811T>A (p.Phe271Ile)
dbSNP
2g.211702026_211702027delCA764258985ERBB4c.1431_1432del (p.Phe478GlnfsTer16)
c.1353_1354del (p.Phe452GlnfsTer16)
c.1430_1431del
c.1254_1255del (p.Phe419GlnfsTer16)
n.1483_1484del
c.1509_1510del (p.Phe504GlnfsTer16)
c.810_811del (p.Phe271GlnfsTer16)
ClinVar dbSNP gnomAD v3 gnomAD v4
2g.211702025G>ACA431130723ERBB4c.1431C>T (p.Leu477=)
c.1353C>T (p.Leu451=)
c.1430C>T
c.1254C>T (p.Leu418=)
n.1483C>T
c.1509C>T (p.Leu503=)
c.810C>T (p.Leu270=)
dbSNP
2g.211702025G>CCA431130725ERBB4c.1431C>G (p.Leu477=)
c.1353C>G (p.Leu451=)
c.1430C>G
c.1254C>G (p.Leu418=)
n.1483C>G
c.1509C>G (p.Leu503=)
c.810C>G (p.Leu270=)
dbSNP COSMIC
2g.211702025G>TCA431130727ERBB4c.1431C>A (p.Leu477=)
c.1353C>A (p.Leu451=)
c.1430C>A
c.1254C>A (p.Leu418=)
n.1483C>A
c.1509C>A (p.Leu503=)
c.810C>A (p.Leu270=)
2g.211702026A=CA1325614767ERBB4c.1430T= (p.Leu477=)
c.1352T= (p.Leu451=)
c.1429T=
c.1253T= (p.Leu418=)
n.1482T=
c.1508T= (p.Leu503=)
c.809T= (p.Leu270=)
2g.211702026A>CCA350442292ERBB4c.1430T>G (p.Leu477Arg)
c.1352T>G (p.Leu451Arg)
c.1429T>G
c.1253T>G (p.Leu418Arg)
n.1482T>G
c.1508T>G (p.Leu503Arg)
c.809T>G (p.Leu270Arg)
dbSNP
2g.211702026A>GCA350442291ERBB4c.1430T>C (p.Leu477Pro)
c.1352T>C (p.Leu451Pro)
c.1429T>C
c.1253T>C (p.Leu418Pro)
n.1482T>C
c.1508T>C (p.Leu503Pro)
c.809T>C (p.Leu270Pro)
2g.211702026A>TCA350442290ERBB4c.1430T>A (p.Leu477His)
c.1352T>A (p.Leu451His)
c.1429T>A
c.1253T>A (p.Leu418His)
n.1482T>A
c.1508T>A (p.Leu503His)
c.809T>A (p.Leu270His)
dbSNP gnomAD v4
2g.211702027G>ACA350442293ERBB4c.1429C>T (p.Leu477Phe)
c.1351C>T (p.Leu451Phe)
c.1428C>T
c.1252C>T (p.Leu418Phe)
n.1481C>T
c.1507C>T (p.Leu503Phe)
c.808C>T (p.Leu270Phe)
gnomAD v4
2g.211702027G>CCA350442294ERBB4c.1429C>G (p.Leu477Val)
c.1351C>G (p.Leu451Val)
c.1428C>G
c.1252C>G (p.Leu418Val)
n.1481C>G
c.1507C>G (p.Leu503Val)
c.808C>G (p.Leu270Val)
dbSNP
2g.211702027G>TCA350442295ERBB4c.1429C>A (p.Leu477Ile)
c.1351C>A (p.Leu451Ile)
c.1428C>A
c.1252C>A (p.Leu418Ile)
n.1481C>A
c.1507C>A (p.Leu503Ile)
c.808C>A (p.Leu270Ile)
dbSNP
2g.211702028T>ACA431130736ERBB4c.1428A>T (p.Thr476=)
c.1350A>T (p.Thr450=)
c.1427A>T
c.1251A>T (p.Thr417=)
n.1480A>T
c.1506A>T (p.Thr502=)
c.807A>T (p.Thr269=)
dbSNP
2g.211702028T>CCA2088134ERBB4c.1428A>G (p.Thr476=)
c.1350A>G (p.Thr450=)
c.1427A>G
c.1251A>G (p.Thr417=)
n.1480A>G
c.1506A>G (p.Thr502=)
c.807A>G (p.Thr269=)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.211702028T>GCA2088135ERBB4c.1428A>C (p.Thr476=)
c.1350A>C (p.Thr450=)
c.1427A>C
c.1251A>C (p.Thr417=)
n.1480A>C
c.1506A>C (p.Thr502=)
c.807A>C (p.Thr269=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.211702028T=CA1325614768ERBB4c.1428A= (p.Thr476=)
c.1350A= (p.Thr450=)
c.1427A=
c.1251A= (p.Thr417=)
n.1480A=
c.1506A= (p.Thr502=)
c.807A= (p.Thr269=)
2g.211702029G>ACA2088136ERBB4c.1427C>T (p.Thr476Ile)
c.1349C>T (p.Thr450Ile)
c.1426C>T
c.1250C>T (p.Thr417Ile)
n.1479C>T
c.1505C>T (p.Thr502Ile)
c.806C>T (p.Thr269Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.211702029G>CCA350442296ERBB4c.1427C>G (p.Thr476Arg)
c.1349C>G (p.Thr450Arg)
c.1426C>G
c.1250C>G (p.Thr417Arg)
n.1479C>G
c.1505C>G (p.Thr502Arg)
c.806C>G (p.Thr269Arg)
dbSNP
2g.211702029G=CA1325614769ERBB4c.1427C= (p.Thr476=)
c.1349C= (p.Thr450=)
c.1426C=
c.1250C= (p.Thr417=)
n.1479C=
c.1505C= (p.Thr502=)
c.806C= (p.Thr269=)
2g.211702029G>TCA350442297ERBB4c.1427C>A (p.Thr476Lys)
c.1349C>A (p.Thr450Lys)
c.1426C>A
c.1250C>A (p.Thr417Lys)
n.1479C>A
c.1505C>A (p.Thr502Lys)
c.806C>A (p.Thr269Lys)
2g.211702030T>ACA350442298ERBB4c.1426A>T (p.Thr476Ser)
c.1348A>T (p.Thr450Ser)
c.1425A>T
c.1249A>T (p.Thr417Ser)
n.1478A>T
c.1504A>T (p.Thr502Ser)
c.805A>T (p.Thr269Ser)
2g.211702030T>CCA2088137ERBB4c.1426A>G (p.Thr476Ala)
c.1348A>G (p.Thr450Ala)
c.1425A>G
c.1249A>G (p.Thr417Ala)
n.1478A>G
c.1504A>G (p.Thr502Ala)
c.805A>G (p.Thr269Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.211702030T>GCA350442299ERBB4c.1426A>C (p.Thr476Pro)
c.1348A>C (p.Thr450Pro)
c.1425A>C
c.1249A>C (p.Thr417Pro)
n.1478A>C
c.1504A>C (p.Thr502Pro)
c.805A>C (p.Thr269Pro)
2g.211702030T=CA1325614770ERBB4c.1426A= (p.Thr476=)
c.1348A= (p.Thr450=)
c.1425A=
c.1249A= (p.Thr417=)
n.1478A=
c.1504A= (p.Thr502=)
c.805A= (p.Thr269=)
2g.211702031T>ACA431130747ERBB4c.1425A>T (p.Thr475=)
c.1347A>T (p.Thr449=)
c.1424A>T
c.1248A>T (p.Thr416=)
n.1477A>T
c.1503A>T (p.Thr501=)
c.804A>T (p.Thr268=)
2g.211702031T>CCA431130748ERBB4c.1425A>G (p.Thr475=)
c.1347A>G (p.Thr449=)
c.1424A>G
c.1248A>G (p.Thr416=)
n.1477A>G
c.1503A>G (p.Thr501=)
c.804A>G (p.Thr268=)
2g.211702031T>GCA431130750ERBB4c.1425A>C (p.Thr475=)
c.1347A>C (p.Thr449=)
c.1424A>C
c.1248A>C (p.Thr416=)
n.1477A>C
c.1503A>C (p.Thr501=)
c.804A>C (p.Thr268=)
dbSNP
2g.211702032G>ACA350442300ERBB4c.1424C>T (p.Thr475Ile)
c.1346C>T (p.Thr449Ile)
c.1423C>T
c.1247C>T (p.Thr416Ile)
n.1476C>T
c.1502C>T (p.Thr501Ile)
c.803C>T (p.Thr268Ile)
2g.211702032G>CCA350442301ERBB4c.1424C>G (p.Thr475Arg)
c.1346C>G (p.Thr449Arg)
c.1423C>G
c.1247C>G (p.Thr416Arg)
n.1476C>G
c.1502C>G (p.Thr501Arg)
c.803C>G (p.Thr268Arg)
dbSNP
2g.211702032G>TCA350442302ERBB4c.1424C>A (p.Thr475Lys)
c.1346C>A (p.Thr449Lys)
c.1423C>A
c.1247C>A (p.Thr416Lys)
n.1476C>A
c.1502C>A (p.Thr501Lys)
c.803C>A (p.Thr268Lys)
dbSNP
2g.211702033T>ACA350442304ERBB4c.1423A>T (p.Thr475Ser)
c.1345A>T (p.Thr449Ser)
c.1422A>T
c.1246A>T (p.Thr416Ser)
n.1475A>T
c.1501A>T (p.Thr501Ser)
c.802A>T (p.Thr268Ser)
2g.211702033T>CCA350442305ERBB4c.1423A>G (p.Thr475Ala)
c.1345A>G (p.Thr449Ala)
c.1422A>G
c.1246A>G (p.Thr416Ala)
n.1475A>G
c.1501A>G (p.Thr501Ala)
c.802A>G (p.Thr268Ala)
2g.211702033T>GCA350442303ERBB4c.1423A>C (p.Thr475Pro)
c.1345A>C (p.Thr449Pro)
c.1422A>C
c.1246A>C (p.Thr416Pro)
n.1475A>C
c.1501A>C (p.Thr501Pro)
c.802A>C (p.Thr268Pro)
COSMIC COSMIC
2g.211702034C>ACA350442306ERBB4c.1422G>T (p.Trp474Cys)
c.1344G>T (p.Trp448Cys)
c.1421G>T
c.1245G>T (p.Trp415Cys)
n.1474G>T
c.1500G>T (p.Trp500Cys)
c.801G>T (p.Trp267Cys)
COSMIC COSMIC
2g.211702034C>GCA350442307ERBB4c.1422G>C (p.Trp474Cys)
c.1344G>C (p.Trp448Cys)
c.1421G>C
c.1245G>C (p.Trp415Cys)
n.1474G>C
c.1500G>C (p.Trp500Cys)
c.801G>C (p.Trp267Cys)
2g.211702034C>TCA350442308ERBB4c.1422G>A (p.Trp474Ter)
c.1344G>A (p.Trp448Ter)
c.1421G>A
c.1245G>A (p.Trp415Ter)
n.1474G>A
c.1500G>A (p.Trp500Ter)
c.801G>A (p.Trp267Ter)
gnomAD v4
2g.211702035C>ACA350442309ERBB4c.1421G>T (p.Trp474Leu)
c.1343G>T (p.Trp448Leu)
c.1420G>T
c.1244G>T (p.Trp415Leu)
n.1473G>T
c.1499G>T (p.Trp500Leu)
c.800G>T (p.Trp267Leu)
dbSNP
2g.211702035C>GCA350442310ERBB4c.1421G>C (p.Trp474Ser)
c.1343G>C (p.Trp448Ser)
c.1420G>C
c.1244G>C (p.Trp415Ser)
n.1473G>C
c.1499G>C (p.Trp500Ser)
c.800G>C (p.Trp267Ser)
dbSNP
2g.211702035C>TCA350442311ERBB4c.1421G>A (p.Trp474Ter)
c.1343G>A (p.Trp448Ter)
c.1420G>A
c.1244G>A (p.Trp415Ter)
n.1473G>A
c.1499G>A (p.Trp500Ter)
c.800G>A (p.Trp267Ter)
dbSNP
2g.211702036A>CCA350442314ERBB4c.1420T>G (p.Trp474Gly)
c.1342T>G (p.Trp448Gly)
c.1419T>G
c.1243T>G (p.Trp415Gly)
n.1472T>G
c.1498T>G (p.Trp500Gly)
c.799T>G (p.Trp267Gly)
2g.211702036A>GCA350442312ERBB4c.1420T>C (p.Trp474Arg)
c.1342T>C (p.Trp448Arg)
c.1419T>C
c.1243T>C (p.Trp415Arg)
n.1472T>C
c.1498T>C (p.Trp500Arg)
c.799T>C (p.Trp267Arg)
2g.211702036A>TCA350442313ERBB4c.1420T>A (p.Trp474Arg)
c.1342T>A (p.Trp448Arg)
c.1419T>A
c.1243T>A (p.Trp415Arg)
n.1472T>A
c.1498T>A (p.Trp500Arg)
c.799T>A (p.Trp267Arg)
2g.211702037G>ACA431130759ERBB4c.1419C>T (p.Asn473=)
c.1341C>T (p.Asn447=)
c.1418C>T
c.1242C>T (p.Asn414=)
n.1471C>T
c.1497C>T (p.Asn499=)
c.798C>T (p.Asn266=)
2g.211702037G>CCA350442315ERBB4c.1419C>G (p.Asn473Lys)
c.1341C>G (p.Asn447Lys)
c.1418C>G
c.1242C>G (p.Asn414Lys)
n.1471C>G
c.1497C>G (p.Asn499Lys)
c.798C>G (p.Asn266Lys)
COSMIC COSMIC
2g.211702037G>TCA350442316ERBB4c.1419C>A (p.Asn473Lys)
c.1341C>A (p.Asn447Lys)
c.1418C>A
c.1242C>A (p.Asn414Lys)
n.1471C>A
c.1497C>A (p.Asn499Lys)
c.798C>A (p.Asn266Lys)
2g.211702038T>ACA350442317ERBB4c.1418A>T (p.Asn473Ile)
c.1340A>T (p.Asn447Ile)
c.1417A>T
c.1241A>T (p.Asn414Ile)
n.1470A>T
c.1496A>T (p.Asn499Ile)
c.797A>T (p.Asn266Ile)
dbSNP
2g.211702038T>CCA350442318ERBB4c.1418A>G (p.Asn473Ser)
c.1340A>G (p.Asn447Ser)
c.1417A>G
c.1241A>G (p.Asn414Ser)
n.1470A>G
c.1496A>G (p.Asn499Ser)
c.797A>G (p.Asn266Ser)
2g.211702038T>GCA350442319ERBB4c.1418A>C (p.Asn473Thr)
c.1340A>C (p.Asn447Thr)
c.1417A>C
c.1241A>C (p.Asn414Thr)
n.1470A>C
c.1496A>C (p.Asn499Thr)
c.797A>C (p.Asn266Thr)
2g.211702039T>ACA350442320ERBB4c.1417A>T (p.Asn473Tyr)
c.1339A>T (p.Asn447Tyr)
c.1416A>T
c.1240A>T (p.Asn414Tyr)
n.1469A>T
c.1495A>T (p.Asn499Tyr)
c.796A>T (p.Asn266Tyr)
2g.211702039T>CCA350442322ERBB4c.1417A>G (p.Asn473Asp)
c.1339A>G (p.Asn447Asp)
c.1416A>G
c.1240A>G (p.Asn414Asp)
n.1469A>G
c.1495A>G (p.Asn499Asp)
c.796A>G (p.Asn266Asp)
2g.211702039T>GCA350442321ERBB4c.1417A>C (p.Asn473His)
c.1339A>C (p.Asn447His)
c.1416A>C
c.1240A>C (p.Asn414His)
n.1469A>C
c.1495A>C (p.Asn499His)
c.796A>C (p.Asn266His)
2g.211702040A>CCA350442323ERBB4c.1416T>G (p.Ile472Met)
c.1338T>G (p.Ile446Met)
c.1415T>G
c.1239T>G (p.Ile413Met)
n.1468T>G
c.1494T>G (p.Ile498Met)
c.795T>G (p.Ile265Met)
2g.211702040A>GCA431130770ERBB4c.1416T>C (p.Ile472=)
c.1338T>C (p.Ile446=)
c.1415T>C
c.1239T>C (p.Ile413=)
n.1468T>C
c.1494T>C (p.Ile498=)
c.795T>C (p.Ile265=)
dbSNP
2g.211702040A>TCA431130771ERBB4c.1416T>A (p.Ile472=)
c.1338T>A (p.Ile446=)
c.1415T>A
c.1239T>A (p.Ile413=)
n.1468T>A
c.1494T>A (p.Ile498=)
c.795T>A (p.Ile265=)
dbSNP
2g.211702041A>CCA350442324ERBB4c.1415T>G (p.Ile472Ser)
c.1337T>G (p.Ile446Ser)
c.1414T>G
c.1238T>G (p.Ile413Ser)
n.1467T>G
c.1493T>G (p.Ile498Ser)
c.794T>G (p.Ile265Ser)
2g.211702041A>GCA350442325ERBB4c.1415T>C (p.Ile472Thr)
c.1337T>C (p.Ile446Thr)
c.1414T>C
c.1238T>C (p.Ile413Thr)
n.1467T>C
c.1493T>C (p.Ile498Thr)
c.794T>C (p.Ile265Thr)
2g.211702041A>TCA350442326ERBB4c.1415T>A (p.Ile472Asn)
c.1337T>A (p.Ile446Asn)
c.1414T>A
c.1238T>A (p.Ile413Asn)
n.1467T>A
c.1493T>A (p.Ile498Asn)
c.794T>A (p.Ile265Asn)
2g.211702042T>ACA350442327ERBB4c.1414A>T (p.Ile472Phe)
c.1336A>T (p.Ile446Phe)
c.1413A>T
c.1237A>T (p.Ile413Phe)
n.1466A>T
c.1492A>T (p.Ile498Phe)
c.793A>T (p.Ile265Phe)
2g.211702042T>CCA2088138ERBB4c.1414A>G (p.Ile472Val)
c.1336A>G (p.Ile446Val)
c.1413A>G
c.1237A>G (p.Ile413Val)
n.1466A>G
c.1492A>G (p.Ile498Val)
c.793A>G (p.Ile265Val)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.211702042T>GCA350442328ERBB4c.1414A>C (p.Ile472Leu)
c.1336A>C (p.Ile446Leu)
c.1413A>C
c.1237A>C (p.Ile413Leu)
n.1466A>C
c.1492A>C (p.Ile498Leu)
c.793A>C (p.Ile265Leu)
2g.211702042T=CA1325614771ERBB4c.1414A= (p.Ile472=)
c.1336A= (p.Ile446=)
c.1413A=
c.1237A= (p.Ile413=)
n.1466A=
c.1492A= (p.Ile498=)
c.793A= (p.Ile265=)
2g.211702043G>ACA431130780ERBB4c.1413C>T (p.Thr471=)
c.1335C>T (p.Thr445=)
c.1412C>T
c.1236C>T (p.Thr412=)
n.1465C>T
c.1491C>T (p.Thr497=)
c.792C>T (p.Thr264=)
dbSNP gnomAD v3 gnomAD v4
2g.211702043G>CCA431130781ERBB4c.1413C>G (p.Thr471=)
c.1335C>G (p.Thr445=)
c.1412C>G
c.1236C>G (p.Thr412=)
n.1465C>G
c.1491C>G (p.Thr497=)
c.792C>G (p.Thr264=)
dbSNP
2g.211702043G=CA1325614772ERBB4c.1413C= (p.Thr471=)
c.1335C= (p.Thr445=)
c.1412C=
c.1236C= (p.Thr412=)
n.1465C=
c.1491C= (p.Thr497=)
c.792C= (p.Thr264=)
2g.211702043G>TCA431130783ERBB4c.1413C>A (p.Thr471=)
c.1335C>A (p.Thr445=)
c.1412C>A
c.1236C>A (p.Thr412=)
n.1465C>A
c.1491C>A (p.Thr497=)
c.792C>A (p.Thr264=)
dbSNP
2g.211702044G>ACA350442329ERBB4c.1412C>T (p.Thr471Ile)
c.1334C>T (p.Thr445Ile)
c.1411C>T
c.1235C>T (p.Thr412Ile)
n.1464C>T
c.1490C>T (p.Thr497Ile)
c.791C>T (p.Thr264Ile)
dbSNP
2g.211702044G>CCA350442330ERBB4c.1412C>G (p.Thr471Ser)
c.1334C>G (p.Thr445Ser)
c.1411C>G
c.1235C>G (p.Thr412Ser)
n.1464C>G
c.1490C>G (p.Thr497Ser)
c.791C>G (p.Thr264Ser)
dbSNP
2g.211702044G>TCA350442331ERBB4c.1412C>A (p.Thr471Asn)
c.1334C>A (p.Thr445Asn)
c.1411C>A
c.1235C>A (p.Thr412Asn)
n.1464C>A
c.1490C>A (p.Thr497Asn)
c.791C>A (p.Thr264Asn)
COSMIC COSMIC
2g.211702045T>ACA350442334ERBB4c.1411A>T (p.Thr471Ser)
c.1333A>T (p.Thr445Ser)
c.1410A>T
c.1234A>T (p.Thr412Ser)
n.1463A>T
c.1489A>T (p.Thr497Ser)
c.790A>T (p.Thr264Ser)
2g.211702045T>CCA350442332ERBB4c.1411A>G (p.Thr471Ala)
c.1333A>G (p.Thr445Ala)
c.1410A>G
c.1234A>G (p.Thr412Ala)
n.1463A>G
c.1489A>G (p.Thr497Ala)
c.790A>G (p.Thr264Ala)
gnomAD v4
2g.211702045T>GCA350442333ERBB4c.1411A>C (p.Thr471Pro)
c.1333A>C (p.Thr445Pro)
c.1410A>C
c.1234A>C (p.Thr412Pro)
n.1463A>C
c.1489A>C (p.Thr497Pro)
c.790A>C (p.Thr264Pro)
2g.211702045_211702047dupCA2662947260ERBB4c.1409_1411dup (p.His470_Thr471insAsn)
c.1331_1333dup (p.His444_Thr445insAsn)
c.1408_1410dup
c.1232_1234dup (p.His411_Thr412insAsn)
n.1461_1463dup
c.1487_1489dup (p.His496_Thr497insAsn)
c.788_790dup (p.His263_Thr264insAsn)
gnomAD v4
2g.211702046A=CA1325614773ERBB4c.1410T= (p.His470=)
c.1332T= (p.His444=)
c.1409T=
c.1233T= (p.His411=)
n.1462T=
c.1488T= (p.His496=)
c.789T= (p.His263=)
2g.211702046A>CCA350442335ERBB4c.1410T>G (p.His470Gln)
c.1332T>G (p.His444Gln)
c.1409T>G
c.1233T>G (p.His411Gln)
n.1462T>G
c.1488T>G (p.His496Gln)
c.789T>G (p.His263Gln)
2g.211702046A>GCA2088139ERBB4c.1410T>C (p.His470=)
c.1332T>C (p.His444=)
c.1409T>C
c.1233T>C (p.His411=)
n.1462T>C
c.1488T>C (p.His496=)
c.789T>C (p.His263=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.211702046A>TCA350442336ERBB4c.1410T>A (p.His470Gln)
c.1332T>A (p.His444Gln)
c.1409T>A
c.1233T>A (p.His411Gln)
n.1462T>A
c.1488T>A (p.His496Gln)
c.789T>A (p.His263Gln)
dbSNP
2g.211702047T>ACA350442337ERBB4c.1409A>T (p.His470Leu)
c.1331A>T (p.His444Leu)
c.1408A>T
c.1232A>T (p.His411Leu)
n.1461A>T
c.1487A>T (p.His496Leu)
c.788A>T (p.His263Leu)
2g.211702047T>CCA350442339ERBB4c.1409A>G (p.His470Arg)
c.1331A>G (p.His444Arg)
c.1408A>G
c.1232A>G (p.His411Arg)
n.1461A>G
c.1487A>G (p.His496Arg)
c.788A>G (p.His263Arg)
dbSNP
2g.211702047T>GCA350442338ERBB4c.1409A>C (p.His470Pro)
c.1331A>C (p.His444Pro)
c.1408A>C
c.1232A>C (p.His411Pro)
n.1461A>C
c.1487A>C (p.His496Pro)
c.788A>C (p.His263Pro)
2g.211702048G>ACA350442340ERBB4c.1408C>T (p.His470Tyr)
c.1330C>T (p.His444Tyr)
c.1407C>T
c.1231C>T (p.His411Tyr)
n.1460C>T
c.1486C>T (p.His496Tyr)
c.787C>T (p.His263Tyr)
dbSNP gnomAD v4
2g.211702048G>CCA350442342ERBB4c.1408C>G (p.His470Asp)
c.1330C>G (p.His444Asp)
c.1407C>G
c.1231C>G (p.His411Asp)
n.1460C>G
c.1486C>G (p.His496Asp)
c.787C>G (p.His263Asp)
dbSNP
2g.211702048G>TCA350442341ERBB4c.1408C>A (p.His470Asn)
c.1330C>A (p.His444Asn)
c.1407C>A
c.1231C>A (p.His411Asn)
n.1460C>A
c.1486C>A (p.His496Asn)
c.787C>A (p.His263Asn)
2g.211702049A>CCA350442343ERBB4c.1407T>G (p.Tyr469Ter)
c.1329T>G (p.Tyr443Ter)
c.1406T>G
c.1230T>G (p.Tyr410Ter)
n.1459T>G
c.1485T>G (p.Tyr495Ter)
c.786T>G (p.Tyr262Ter)
2g.211702049A>GCA431130802ERBB4c.1407T>C (p.Tyr469=)
c.1329T>C (p.Tyr443=)
c.1406T>C
c.1230T>C (p.Tyr410=)
n.1459T>C
c.1485T>C (p.Tyr495=)
c.786T>C (p.Tyr262=)
dbSNP
2g.211702049A>TCA350442344ERBB4c.1407T>A (p.Tyr469Ter)
c.1329T>A (p.Tyr443Ter)
c.1406T>A
c.1230T>A (p.Tyr410Ter)
n.1459T>A
c.1485T>A (p.Tyr495Ter)
c.786T>A (p.Tyr262Ter)
2g.211702050T>ACA350442345ERBB4c.1406A>T (p.Tyr469Phe)
c.1328A>T (p.Tyr443Phe)
c.1405A>T
c.1229A>T (p.Tyr410Phe)
n.1458A>T
c.1484A>T (p.Tyr495Phe)
c.785A>T (p.Tyr262Phe)
dbSNP
2g.211702050T>CCA2088140ERBB4c.1406A>G (p.Tyr469Cys)
c.1328A>G (p.Tyr443Cys)
c.1405A>G
c.1229A>G (p.Tyr410Cys)
n.1458A>G
c.1484A>G (p.Tyr495Cys)
c.785A>G (p.Tyr262Cys)
dbSNP ExAC gnomAD v3 gnomAD v4
2g.211702050T>GCA350442346ERBB4c.1406A>C (p.Tyr469Ser)
c.1328A>C (p.Tyr443Ser)
c.1405A>C
c.1229A>C (p.Tyr410Ser)
n.1458A>C
c.1484A>C (p.Tyr495Ser)
c.785A>C (p.Tyr262Ser)
2g.211702050T=CA1325614774ERBB4c.1406A= (p.Tyr469=)
c.1328A= (p.Tyr443=)
c.1405A=
c.1229A= (p.Tyr410=)
n.1458A=
c.1484A= (p.Tyr495=)
c.785A= (p.Tyr262=)
2g.211702051A>CCA350442347ERBB4c.1405T>G (p.Tyr469Asp)
c.1327T>G (p.Tyr443Asp)
c.1404T>G
c.1228T>G (p.Tyr410Asp)
n.1457T>G
c.1483T>G (p.Tyr495Asp)
c.784T>G (p.Tyr262Asp)
2g.211702051A>GCA350442348ERBB4c.1405T>C (p.Tyr469His)
c.1327T>C (p.Tyr443His)
c.1404T>C
c.1228T>C (p.Tyr410His)
n.1457T>C
c.1483T>C (p.Tyr495His)
c.784T>C (p.Tyr262His)
2g.211702051A>TCA350442349ERBB4c.1405T>A (p.Tyr469Asn)
c.1327T>A (p.Tyr443Asn)
c.1404T>A
c.1228T>A (p.Tyr410Asn)
n.1457T>A
c.1483T>A (p.Tyr495Asn)
c.784T>A (p.Tyr262Asn)
dbSNP
2g.211702052A=CA1325614775ERBB4c.1404T= (p.Tyr468=)
c.1326T= (p.Tyr442=)
c.1403T=
c.1227T= (p.Tyr409=)
n.1456T=
c.1482T= (p.Tyr494=)
c.783T= (p.Tyr261=)
2g.211702052A>CCA350442350ERBB4c.1404T>G (p.Tyr468Ter)
c.1326T>G (p.Tyr442Ter)
c.1403T>G
c.1227T>G (p.Tyr409Ter)
n.1456T>G
c.1482T>G (p.Tyr494Ter)
c.783T>G (p.Tyr261Ter)
2g.211702052A>GCA2088141ERBB4c.1404T>C (p.Tyr468=)
c.1326T>C (p.Tyr442=)
c.1403T>C
c.1227T>C (p.Tyr409=)
n.1456T>C
c.1482T>C (p.Tyr494=)
c.783T>C (p.Tyr261=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.211702052A>TCA350442351ERBB4c.1404T>A (p.Tyr468Ter)
c.1326T>A (p.Tyr442Ter)
c.1403T>A
c.1227T>A (p.Tyr409Ter)
n.1456T>A
c.1482T>A (p.Tyr494Ter)
c.783T>A (p.Tyr261Ter)
2g.211702053T>ACA350442352ERBB4c.1403A>T (p.Tyr468Phe)
c.1325A>T (p.Tyr442Phe)
c.1402A>T
c.1226A>T (p.Tyr409Phe)
n.1455A>T
c.1481A>T (p.Tyr494Phe)
c.782A>T (p.Tyr261Phe)
dbSNP COSMIC COSMIC
2g.211702053T>CCA350442353ERBB4c.1403A>G (p.Tyr468Cys)
c.1325A>G (p.Tyr442Cys)
c.1402A>G
c.1226A>G (p.Tyr409Cys)
n.1455A>G
c.1481A>G (p.Tyr494Cys)
c.782A>G (p.Tyr261Cys)
2g.211702053T>GCA350442354ERBB4c.1403A>C (p.Tyr468Ser)
c.1325A>C (p.Tyr442Ser)
c.1402A>C
c.1226A>C (p.Tyr409Ser)
n.1455A>C
c.1481A>C (p.Tyr494Ser)
c.782A>C (p.Tyr261Ser)
2g.211702054A>CCA350442357ERBB4c.1402T>G (p.Tyr468Asp)
c.1324T>G (p.Tyr442Asp)
c.1401T>G
c.1225T>G (p.Tyr409Asp)
n.1454T>G
c.1480T>G (p.Tyr494Asp)
c.781T>G (p.Tyr261Asp)
2g.211702054A>GCA350442355ERBB4c.1402T>C (p.Tyr468His)
c.1324T>C (p.Tyr442His)
c.1401T>C
c.1225T>C (p.Tyr409His)
n.1454T>C
c.1480T>C (p.Tyr494His)
c.781T>C (p.Tyr261His)
2g.211702054A>TCA350442356ERBB4c.1402T>A (p.Tyr468Asn)
c.1324T>A (p.Tyr442Asn)
c.1401T>A
c.1225T>A (p.Tyr409Asn)
n.1454T>A
c.1480T>A (p.Tyr494Asn)
c.781T>A (p.Tyr261Asn)
2g.211702055A>CCA350442358ERBB4c.1401T>G (p.Cys467Trp)
c.1323T>G (p.Cys441Trp)
c.1400T>G
c.1224T>G (p.Cys408Trp)
n.1453T>G
c.1479T>G (p.Cys493Trp)
c.780T>G (p.Cys260Trp)
2g.211702055A>GCA431130827ERBB4c.1401T>C (p.Cys467=)
c.1323T>C (p.Cys441=)
c.1400T>C
c.1224T>C (p.Cys408=)
n.1453T>C
c.1479T>C (p.Cys493=)
c.780T>C (p.Cys260=)
2g.211702055A>TCA350442359ERBB4c.1401T>A (p.Cys467Ter)
c.1323T>A (p.Cys441Ter)
c.1400T>A
c.1224T>A (p.Cys408Ter)
n.1453T>A
c.1479T>A (p.Cys493Ter)
c.780T>A (p.Cys260Ter)
2g.211702056C>ACA350442360ERBB4c.1400G>T (p.Cys467Phe)
c.1322G>T (p.Cys441Phe)
c.1399G>T
c.1223G>T (p.Cys408Phe)
n.1452G>T
c.1478G>T (p.Cys493Phe)
c.779G>T (p.Cys260Phe)
dbSNP
2g.211702056C>GCA350442361ERBB4c.1400G>C (p.Cys467Ser)
c.1322G>C (p.Cys441Ser)
c.1399G>C
c.1223G>C (p.Cys408Ser)
n.1452G>C
c.1478G>C (p.Cys493Ser)
c.779G>C (p.Cys260Ser)
dbSNP
2g.211702056C>TCA350442362ERBB4c.1400G>A (p.Cys467Tyr)
c.1322G>A (p.Cys441Tyr)
c.1399G>A
c.1223G>A (p.Cys408Tyr)
n.1452G>A
c.1478G>A (p.Cys493Tyr)
c.779G>A (p.Cys260Tyr)
dbSNP
2g.211702057A>CCA350442363ERBB4c.1399T>G (p.Cys467Gly)
c.1321T>G (p.Cys441Gly)
c.1398T>G
c.1222T>G (p.Cys408Gly)
n.1451T>G
c.1477T>G (p.Cys493Gly)
c.778T>G (p.Cys260Gly)
2g.211702057A>GCA350442364ERBB4c.1399T>C (p.Cys467Arg)
c.1321T>C (p.Cys441Arg)
c.1398T>C
c.1222T>C (p.Cys408Arg)
n.1451T>C
c.1477T>C (p.Cys493Arg)
c.778T>C (p.Cys260Arg)
gnomAD v4
2g.211702057A>TCA350442365ERBB4c.1399T>A (p.Cys467Ser)
c.1321T>A (p.Cys441Ser)
c.1398T>A
c.1222T>A (p.Cys408Ser)
n.1451T>A
c.1477T>A (p.Cys493Ser)
c.778T>A (p.Cys260Ser)
dbSNP
2g.211702058C>ACA431130832ERBB4c.1398G>T (p.Leu466=)
c.1320G>T (p.Leu440=)
c.1397G>T
c.1221G>T (p.Leu407=)
n.1450G>T
c.1476G>T (p.Leu492=)
c.777G>T (p.Leu259=)
2g.211702058C>GCA431130835ERBB4c.1398G>C (p.Leu466=)
c.1320G>C (p.Leu440=)
c.1397G>C
c.1221G>C (p.Leu407=)
n.1450G>C
c.1476G>C (p.Leu492=)
c.777G>C (p.Leu259=)
dbSNP
2g.211702058C>TCA431130833ERBB4c.1398G>A (p.Leu466=)
c.1320G>A (p.Leu440=)
c.1397G>A
c.1221G>A (p.Leu407=)
n.1450G>A
c.1476G>A (p.Leu492=)
c.777G>A (p.Leu259=)
2g.211702059A>CCA350442366ERBB4c.1397T>G (p.Leu466Arg)
c.1319T>G (p.Leu440Arg)
c.1396T>G
c.1220T>G (p.Leu407Arg)
n.1449T>G
c.1475T>G (p.Leu492Arg)
c.776T>G (p.Leu259Arg)
2g.211702059A>GCA350442367ERBB4c.1397T>C (p.Leu466Pro)
c.1319T>C (p.Leu440Pro)
c.1396T>C
c.1220T>C (p.Leu407Pro)
n.1449T>C
c.1475T>C (p.Leu492Pro)
c.776T>C (p.Leu259Pro)
2g.211702059A>TCA350442368ERBB4c.1397T>A (p.Leu466Gln)
c.1319T>A (p.Leu440Gln)
c.1396T>A
c.1220T>A (p.Leu407Gln)
n.1449T>A
c.1475T>A (p.Leu492Gln)
c.776T>A (p.Leu259Gln)
2g.211702060G>ACA64751905ERBB4c.1396C>T (p.Leu466=)
c.1318C>T (p.Leu440=)
c.1395C>T
c.1219C>T (p.Leu407=)
n.1448C>T
c.1474C>T (p.Leu492=)
c.775C>T (p.Leu259=)
dbSNP
2g.211702060G>CCA350442369ERBB4c.1396C>G (p.Leu466Val)
c.1318C>G (p.Leu440Val)
c.1395C>G
c.1219C>G (p.Leu407Val)
n.1448C>G
c.1474C>G (p.Leu492Val)
c.775C>G (p.Leu259Val)
2g.211702060G=CA1325614776ERBB4c.1396C= (p.Leu466=)
c.1318C= (p.Leu440=)
c.1395C=
c.1219C= (p.Leu407=)
n.1448C=
c.1474C= (p.Leu492=)
c.775C= (p.Leu259=)
2g.211702060G>TCA350442370ERBB4c.1396C>A (p.Leu466Met)
c.1318C>A (p.Leu440Met)
c.1395C>A
c.1219C>A (p.Leu407Met)
n.1448C>A
c.1474C>A (p.Leu492Met)
c.775C>A (p.Leu259Met)
dbSNP gnomAD v4
2g.211702061G>ACA431130842ERBB4c.1395C>T (p.Asn465=)
c.1317C>T (p.Asn439=)
c.1394C>T
c.1218C>T (p.Asn406=)
n.1447C>T
c.1473C>T (p.Asn491=)
c.774C>T (p.Asn258=)
dbSNP gnomAD v4
2g.211702061G>CCA350442371ERBB4c.1395C>G (p.Asn465Lys)
c.1317C>G (p.Asn439Lys)
c.1394C>G
c.1218C>G (p.Asn406Lys)
n.1447C>G
c.1473C>G (p.Asn491Lys)
c.774C>G (p.Asn258Lys)
dbSNP
2g.211702061G=CA1325614777ERBB4c.1395C= (p.Asn465=)
c.1317C= (p.Asn439=)
c.1394C=
c.1218C= (p.Asn406=)
n.1447C=
c.1473C= (p.Asn491=)
c.774C= (p.Asn258=)
2g.211702061G>TCA2088142ERBB4c.1395C>A (p.Asn465Lys)
c.1317C>A (p.Asn439Lys)
c.1394C>A
c.1218C>A (p.Asn406Lys)
n.1447C>A
c.1473C>A (p.Asn491Lys)
c.774C>A (p.Asn258Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.211702062T>ACA350442372ERBB4c.1394A>T (p.Asn465Ile)
c.1316A>T (p.Asn439Ile)
c.1393A>T
c.1217A>T (p.Asn406Ile)
n.1446A>T
c.1472A>T (p.Asn491Ile)
c.773A>T (p.Asn258Ile)
dbSNP
2g.211702062T>CCA350442373ERBB4c.1394A>G (p.Asn465Ser)
c.1316A>G (p.Asn439Ser)
c.1393A>G
c.1217A>G (p.Asn406Ser)
n.1446A>G
c.1472A>G (p.Asn491Ser)
c.773A>G (p.Asn258Ser)
2g.211702062T>GCA350442374ERBB4c.1394A>C (p.Asn465Thr)
c.1316A>C (p.Asn439Thr)
c.1393A>C
c.1217A>C (p.Asn406Thr)
n.1446A>C
c.1472A>C (p.Asn491Thr)
c.773A>C (p.Asn258Thr)
dbSNP
2g.211702063T>ACA350442375ERBB4c.1393A>T (p.Asn465Tyr)
c.1315A>T (p.Asn439Tyr)
c.1392A>T
c.1216A>T (p.Asn406Tyr)
n.1445A>T
c.1471A>T (p.Asn491Tyr)
c.772A>T (p.Asn258Tyr)
2g.211702063T>CCA350442376ERBB4c.1393A>G (p.Asn465Asp)
c.1315A>G (p.Asn439Asp)
c.1392A>G
c.1216A>G (p.Asn406Asp)
n.1445A>G
c.1471A>G (p.Asn491Asp)
c.772A>G (p.Asn258Asp)
2g.211702063T>GCA350442377ERBB4c.1393A>C (p.Asn465His)
c.1315A>C (p.Asn439His)
c.1392A>C
c.1216A>C (p.Asn406His)
n.1445A>C
c.1471A>C (p.Asn491His)
c.772A>C (p.Asn258His)
2g.211702064G>ACA431130849ERBB4c.1392C>T (p.Ser464=)
c.1314C>T (p.Ser438=)
c.1391C>T
c.1215C>T (p.Ser405=)
n.1444C>T
c.1470C>T (p.Ser490=)
c.771C>T (p.Ser257=)
dbSNP
2g.211702064G>CCA350442378ERBB4c.1392C>G (p.Ser464Arg)
c.1314C>G (p.Ser438Arg)
c.1391C>G
c.1215C>G (p.Ser405Arg)
n.1444C>G
c.1470C>G (p.Ser490Arg)
c.771C>G (p.Ser257Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.211702064G=CA1325614778ERBB4c.1392C= (p.Ser464=)
c.1314C= (p.Ser438=)
c.1391C=
c.1215C= (p.Ser405=)
n.1444C=
c.1470C= (p.Ser490=)
c.771C= (p.Ser257=)
2g.211702064G>TCA350442379ERBB4c.1392C>A (p.Ser464Arg)
c.1314C>A (p.Ser438Arg)
c.1391C>A
c.1215C>A (p.Ser405Arg)
n.1444C>A
c.1470C>A (p.Ser490Arg)
c.771C>A (p.Ser257Arg)
2g.211702065C>ACA350442380ERBB4c.1391G>T (p.Ser464Ile)
c.1313G>T (p.Ser438Ile)
c.1390G>T
c.1214G>T (p.Ser405Ile)
n.1443G>T
c.1469G>T (p.Ser490Ile)
c.770G>T (p.Ser257Ile)
2g.211702065C>GCA350442381ERBB4c.1391G>C (p.Ser464Thr)
c.1313G>C (p.Ser438Thr)
c.1390G>C
c.1214G>C (p.Ser405Thr)
n.1443G>C
c.1469G>C (p.Ser490Thr)
c.770G>C (p.Ser257Thr)
dbSNP
2g.211702065C>TCA350442382ERBB4c.1391G>A (p.Ser464Asn)
c.1313G>A (p.Ser438Asn)
c.1390G>A
c.1214G>A (p.Ser405Asn)
n.1443G>A
c.1469G>A (p.Ser490Asn)
c.770G>A (p.Ser257Asn)
dbSNP gnomAD v4
2g.211702066T>ACA350442383ERBB4c.1390A>T (p.Ser464Cys)
c.1312A>T (p.Ser438Cys)
c.1389A>T
c.1213A>T (p.Ser405Cys)
n.1442A>T
c.1468A>T (p.Ser490Cys)
c.769A>T (p.Ser257Cys)
2g.211702066T>CCA350442385ERBB4c.1390A>G (p.Ser464Gly)
c.1312A>G (p.Ser438Gly)
c.1389A>G
c.1213A>G (p.Ser405Gly)
n.1442A>G
c.1468A>G (p.Ser490Gly)
c.769A>G (p.Ser257Gly)
gnomAD v4 COSMIC COSMIC
2g.211702066T>GCA350442384ERBB4c.1390A>C (p.Ser464Arg)
c.1312A>C (p.Ser438Arg)
c.1389A>C
c.1213A>C (p.Ser405Arg)
n.1442A>C
c.1468A>C (p.Ser490Arg)
c.769A>C (p.Ser257Arg)
2g.211702067G>ACA431130865ERBB4c.1389C>T (p.Asn463=)
c.1311C>T (p.Asn437=)
c.1388C>T
c.1212C>T (p.Asn404=)
n.1441C>T
c.1467C>T (p.Asn489=)
c.768C>T (p.Asn256=)
dbSNP
2g.211702067G>CCA350442386ERBB4c.1389C>G (p.Asn463Lys)
c.1311C>G (p.Asn437Lys)
c.1388C>G
c.1212C>G (p.Asn404Lys)
n.1441C>G
c.1467C>G (p.Asn489Lys)
c.768C>G (p.Asn256Lys)
dbSNP
2g.211702067G>TCA350442387ERBB4c.1389C>A (p.Asn463Lys)
c.1311C>A (p.Asn437Lys)
c.1388C>A
c.1212C>A (p.Asn404Lys)
n.1441C>A
c.1467C>A (p.Asn489Lys)
c.768C>A (p.Asn256Lys)
dbSNP
2g.211702068T>ACA350442388ERBB4c.1388A>T (p.Asn463Ile)
c.1310A>T (p.Asn437Ile)
c.1387A>T
c.1211A>T (p.Asn404Ile)
n.1440A>T
c.1466A>T (p.Asn489Ile)
c.767A>T (p.Asn256Ile)
dbSNP
2g.211702068T>CCA350442389ERBB4c.1388A>G (p.Asn463Ser)
c.1310A>G (p.Asn437Ser)
c.1387A>G
c.1211A>G (p.Asn404Ser)
n.1440A>G
c.1466A>G (p.Asn489Ser)
c.767A>G (p.Asn256Ser)
2g.211702068T>GCA350442390ERBB4c.1388A>C (p.Asn463Thr)
c.1310A>C (p.Asn437Thr)
c.1387A>C
c.1211A>C (p.Asn404Thr)
n.1440A>C
c.1466A>C (p.Asn489Thr)
c.767A>C (p.Asn256Thr)
2g.211702069T>ACA350442391ERBB4c.1387A>T (p.Asn463Tyr)
c.1309A>T (p.Asn437Tyr)
c.1386A>T
c.1210A>T (p.Asn404Tyr)
n.1439A>T
c.1465A>T (p.Asn489Tyr)
c.766A>T (p.Asn256Tyr)
2g.211702069T>CCA350442392ERBB4c.1387A>G (p.Asn463Asp)
c.1309A>G (p.Asn437Asp)
c.1386A>G
c.1210A>G (p.Asn404Asp)
n.1439A>G
c.1465A>G (p.Asn489Asp)
c.766A>G (p.Asn256Asp)
2g.211702069T>GCA350442393ERBB4c.1387A>C (p.Asn463His)
c.1309A>C (p.Asn437His)
c.1386A>C
c.1210A>C (p.Asn404His)
n.1439A>C
c.1465A>C (p.Asn489His)
c.766A>C (p.Asn256His)
2g.211702070G>ACA431130880ERBB4c.1386C>T (p.Asp462=)
c.1308C>T (p.Asp436=)
c.1385C>T
c.1209C>T (p.Asp403=)
n.1438C>T
c.1464C>T (p.Asp488=)
c.765C>T (p.Asp255=)
dbSNP
2g.211702070G>CCA350442394ERBB4c.1386C>G (p.Asp462Glu)
c.1308C>G (p.Asp436Glu)
c.1385C>G
c.1209C>G (p.Asp403Glu)
n.1438C>G
c.1464C>G (p.Asp488Glu)
c.765C>G (p.Asp255Glu)
2g.211702070G=CA1325614779ERBB4c.1386C= (p.Asp462=)
c.1308C= (p.Asp436=)
c.1385C=
c.1209C= (p.Asp403=)
n.1438C=
c.1464C= (p.Asp488=)
c.765C= (p.Asp255=)
2g.211702070G>TCA350442395ERBB4c.1386C>A (p.Asp462Glu)
c.1308C>A (p.Asp436Glu)
c.1385C>A
c.1209C>A (p.Asp403Glu)
n.1438C>A
c.1464C>A (p.Asp488Glu)
c.765C>A (p.Asp255Glu)
dbSNP gnomAD v3 gnomAD v4
2g.211702072_211702075delCA2577232940ERBB4c.1383_1386del (p.Asp462ThrfsTer23)
c.1305_1308del (p.Asp436ThrfsTer23)
c.1382_1385del
c.1206_1209del (p.Asp403ThrfsTer23)
n.1435_1438del
c.1461_1464del (p.Asp488ThrfsTer23)
c.762_765del (p.Asp255ThrfsTer23)
2g.211702071T>ACA350442398ERBB4c.1385A>T (p.Asp462Val)
c.1307A>T (p.Asp436Val)
c.1384A>T
c.1208A>T (p.Asp403Val)
n.1437A>T
c.1463A>T (p.Asp488Val)
c.764A>T (p.Asp255Val)
dbSNP
2g.211702071T>CCA350442397ERBB4c.1385A>G (p.Asp462Gly)
c.1307A>G (p.Asp436Gly)
c.1384A>G
c.1208A>G (p.Asp403Gly)
n.1437A>G
c.1463A>G (p.Asp488Gly)
c.764A>G (p.Asp255Gly)
dbSNP
2g.211702071T>GCA350442396ERBB4c.1385A>C (p.Asp462Ala)
c.1307A>C (p.Asp436Ala)
c.1384A>C
c.1208A>C (p.Asp403Ala)
n.1437A>C
c.1463A>C (p.Asp488Ala)
c.764A>C (p.Asp255Ala)
dbSNP
2g.211702072C>ACA350442399ERBB4c.1384G>T (p.Asp462Tyr)
c.1306G>T (p.Asp436Tyr)
c.1383G>T
c.1207G>T (p.Asp403Tyr)
n.1436G>T
c.1462G>T (p.Asp488Tyr)
c.763G>T (p.Asp255Tyr)
dbSNP
2g.211702072C>GCA350442401ERBB4c.1384G>C (p.Asp462His)
c.1306G>C (p.Asp436His)
c.1383G>C
c.1207G>C (p.Asp403His)
n.1436G>C
c.1462G>C (p.Asp488His)
c.763G>C (p.Asp255His)
dbSNP
2g.211702072C>TCA350442400ERBB4c.1384G>A (p.Asp462Asn)
c.1306G>A (p.Asp436Asn)
c.1383G>A
c.1207G>A (p.Asp403Asn)
n.1436G>A
c.1462G>A (p.Asp488Asn)
c.763G>A (p.Asp255Asn)
dbSNP
2g.211702073A>CCA431130885ERBB4c.1383T>G (p.Thr461=)
c.1305T>G (p.Thr435=)
c.1382T>G
c.1206T>G (p.Thr402=)
n.1435T>G
c.1461T>G (p.Thr487=)
c.762T>G (p.Thr254=)
2g.211702073A>GCA431130886ERBB4c.1383T>C (p.Thr461=)
c.1305T>C (p.Thr435=)
c.1382T>C
c.1206T>C (p.Thr402=)
n.1435T>C
c.1461T>C (p.Thr487=)
c.762T>C (p.Thr254=)
2g.211702073A>TCA431130887ERBB4c.1383T>A (p.Thr461=)
c.1305T>A (p.Thr435=)
c.1382T>A
c.1206T>A (p.Thr402=)
n.1435T>A
c.1461T>A (p.Thr487=)
c.762T>A (p.Thr254=)
2g.211702074G>ACA350442402ERBB4c.1382C>T (p.Thr461Ile)
c.1304C>T (p.Thr435Ile)
c.1381C>T
c.1205C>T (p.Thr402Ile)
n.1434C>T
c.1460C>T (p.Thr487Ile)
c.761C>T (p.Thr254Ile)
dbSNP
2g.211702074G>CCA350442403ERBB4c.1382C>G (p.Thr461Ser)
c.1304C>G (p.Thr435Ser)
c.1381C>G
c.1205C>G (p.Thr402Ser)
n.1434C>G
c.1460C>G (p.Thr487Ser)
c.761C>G (p.Thr254Ser)
dbSNP gnomAD v2 gnomAD v4
2g.211702074G=CA1325614780ERBB4c.1382C= (p.Thr461=)
c.1304C= (p.Thr435=)
c.1381C=
c.1205C= (p.Thr402=)
n.1434C=
c.1460C= (p.Thr487=)
c.761C= (p.Thr254=)
2g.211702074G>TCA350442404ERBB4c.1382C>A (p.Thr461Asn)
c.1304C>A (p.Thr435Asn)
c.1381C>A
c.1205C>A (p.Thr402Asn)
n.1434C>A
c.1460C>A (p.Thr487Asn)
c.761C>A (p.Thr254Asn)
2g.211702075T>ACA350442405ERBB4c.1381A>T (p.Thr461Ser)
c.1303A>T (p.Thr435Ser)
c.1380A>T
c.1204A>T (p.Thr402Ser)
n.1433A>T
c.1459A>T (p.Thr487Ser)
c.760A>T (p.Thr254Ser)
dbSNP
2g.211702075T>CCA350442406ERBB4c.1381A>G (p.Thr461Ala)
c.1303A>G (p.Thr435Ala)
c.1380A>G
c.1204A>G (p.Thr402Ala)
n.1433A>G
c.1459A>G (p.Thr487Ala)
c.760A>G (p.Thr254Ala)
dbSNP COSMIC
2g.211702075T>GCA350442407ERBB4c.1381A>C (p.Thr461Pro)
c.1303A>C (p.Thr435Pro)
c.1380A>C
c.1204A>C (p.Thr402Pro)
n.1433A>C
c.1459A>C (p.Thr487Pro)
c.760A>C (p.Thr254Pro)
2g.211702075T=CA1325614781ERBB4c.1381A= (p.Thr461=)
c.1303A= (p.Thr435=)
c.1380A=
c.1204A= (p.Thr402=)
n.1433A=
c.1459A= (p.Thr487=)
c.760A= (p.Thr254=)
2g.211702076A>CCA350442408ERBB4c.1380T>G (p.Ile460Met)
c.1302T>G (p.Ile434Met)
c.1379T>G
c.1203T>G (p.Ile401Met)
n.1432T>G
c.1458T>G (p.Ile486Met)
c.759T>G (p.Ile253Met)
2g.211702076A>GCA431130899ERBB4c.1380T>C (p.Ile460=)
c.1302T>C (p.Ile434=)
c.1379T>C
c.1203T>C (p.Ile401=)
n.1432T>C
c.1458T>C (p.Ile486=)
c.759T>C (p.Ile253=)
2g.211702076A>TCA431130900ERBB4c.1380T>A (p.Ile460=)
c.1302T>A (p.Ile434=)
c.1379T>A
c.1203T>A (p.Ile401=)
n.1432T>A
c.1458T>A (p.Ile486=)
c.759T>A (p.Ile253=)
2g.211702077A>CCA350442409ERBB4c.1379T>G (p.Ile460Ser)
c.1301T>G (p.Ile434Ser)
c.1378T>G
c.1202T>G (p.Ile401Ser)
n.1431T>G
c.1457T>G (p.Ile486Ser)
c.758T>G (p.Ile253Ser)
2g.211702077A>GCA350442410ERBB4c.1379T>C (p.Ile460Thr)
c.1301T>C (p.Ile434Thr)
c.1378T>C
c.1202T>C (p.Ile401Thr)
n.1431T>C
c.1457T>C (p.Ile486Thr)
c.758T>C (p.Ile253Thr)
2g.211702077A>TCA350442411ERBB4c.1379T>A (p.Ile460Asn)
c.1301T>A (p.Ile434Asn)
c.1378T>A
c.1202T>A (p.Ile401Asn)
n.1431T>A
c.1457T>A (p.Ile486Asn)
c.758T>A (p.Ile253Asn)
2g.211702078T>ACA350442412ERBB4c.1378A>T (p.Ile460Phe)
c.1300A>T (p.Ile434Phe)
c.1377A>T
c.1201A>T (p.Ile401Phe)
n.1430A>T
c.1456A>T (p.Ile486Phe)
c.757A>T (p.Ile253Phe)
dbSNP
2g.211702078T>CCA2088143ERBB4c.1378A>G (p.Ile460Val)
c.1300A>G (p.Ile434Val)
c.1377A>G
c.1201A>G (p.Ile401Val)
n.1430A>G
c.1456A>G (p.Ile486Val)
c.757A>G (p.Ile253Val)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.211702078T>GCA2088144ERBB4c.1378A>C (p.Ile460Leu)
c.1300A>C (p.Ile434Leu)
c.1377A>C
c.1201A>C (p.Ile401Leu)
n.1430A>C
c.1456A>C (p.Ile486Leu)
c.757A>C (p.Ile253Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.211702078T=CA1325614782ERBB4c.1378A= (p.Ile460=)
c.1300A= (p.Ile434=)
c.1377A=
c.1201A= (p.Ile401=)
n.1430A=
c.1456A= (p.Ile486=)
c.757A= (p.Ile253=)
2g.211702079A>CCA350442413ERBB4c.1377T>G (p.Tyr459Ter)
c.1299T>G (p.Tyr433Ter)
c.1376T>G
c.1200T>G (p.Tyr400Ter)
n.1429T>G
c.1455T>G (p.Tyr485Ter)
c.756T>G (p.Tyr252Ter)
2g.211702079A>GCA431130906ERBB4c.1377T>C (p.Tyr459=)
c.1299T>C (p.Tyr433=)
c.1376T>C
c.1200T>C (p.Tyr400=)
n.1429T>C
c.1455T>C (p.Tyr485=)
c.756T>C (p.Tyr252=)
2g.211702079A>TCA350442414ERBB4c.1377T>A (p.Tyr459Ter)
c.1299T>A (p.Tyr433Ter)
c.1376T>A
c.1200T>A (p.Tyr400Ter)
n.1429T>A
c.1455T>A (p.Tyr485Ter)
c.756T>A (p.Tyr252Ter)
2g.211702080T>ACA350442415ERBB4c.1376A>T (p.Tyr459Phe)
c.1298A>T (p.Tyr433Phe)
c.1375A>T
c.1199A>T (p.Tyr400Phe)
n.1428A>T
c.1454A>T (p.Tyr485Phe)
c.755A>T (p.Tyr252Phe)
dbSNP
2g.211702080T>CCA64751937ERBB4c.1376A>G (p.Tyr459Cys)
c.1298A>G (p.Tyr433Cys)
c.1375A>G
c.1199A>G (p.Tyr400Cys)
n.1428A>G
c.1454A>G (p.Tyr485Cys)
c.755A>G (p.Tyr252Cys)
dbSNP gnomAD v4
2g.211702080T>GCA350442416ERBB4c.1376A>C (p.Tyr459Ser)
c.1298A>C (p.Tyr433Ser)
c.1375A>C
c.1199A>C (p.Tyr400Ser)
n.1428A>C
c.1454A>C (p.Tyr485Ser)
c.755A>C (p.Tyr252Ser)
2g.211702080T=CA1325614783ERBB4c.1376A= (p.Tyr459=)
c.1298A= (p.Tyr433=)
c.1375A=
c.1199A= (p.Tyr400=)
n.1428A=
c.1454A= (p.Tyr485=)
c.755A= (p.Tyr252=)
2g.211702081A>CCA350442417ERBB4c.1375T>G (p.Tyr459Asp)
c.1297T>G (p.Tyr433Asp)
c.1374T>G
c.1198T>G (p.Tyr400Asp)
n.1427T>G
c.1453T>G (p.Tyr485Asp)
c.754T>G (p.Tyr252Asp)
2g.211702081A>GCA350442418ERBB4c.1375T>C (p.Tyr459His)
c.1297T>C (p.Tyr433His)
c.1374T>C
c.1198T>C (p.Tyr400His)
n.1427T>C
c.1453T>C (p.Tyr485His)
c.754T>C (p.Tyr252His)
2g.211702081A>TCA350442419ERBB4c.1375T>A (p.Tyr459Asn)
c.1297T>A (p.Tyr433Asn)
c.1374T>A
c.1198T>A (p.Tyr400Asn)
n.1427T>A
c.1453T>A (p.Tyr485Asn)
c.754T>A (p.Tyr252Asn)
COSMIC
2g.211702082G>ACA431130913ERBB4c.1374C>T (p.Ile458=)
c.1296C>T (p.Ile432=)
c.1373C>T
c.1197C>T (p.Ile399=)
n.1426C>T
c.1452C>T (p.Ile484=)
c.753C>T (p.Ile251=)
dbSNP gnomAD v4 COSMIC COSMIC
2g.211702082G>CCA350442420ERBB4c.1374C>G (p.Ile458Met)
c.1296C>G (p.Ile432Met)
c.1373C>G
c.1197C>G (p.Ile399Met)
n.1426C>G
c.1452C>G (p.Ile484Met)
c.753C>G (p.Ile251Met)
dbSNP
2g.211702082G>TCA431130916ERBB4c.1374C>A (p.Ile458=)
c.1296C>A (p.Ile432=)
c.1373C>A
c.1197C>A (p.Ile399=)
n.1426C>A
c.1452C>A (p.Ile484=)
c.753C>A (p.Ile251=)
2g.211702083A>CCA350442421ERBB4c.1373T>G (p.Ile458Ser)
c.1295T>G (p.Ile432Ser)
c.1372T>G
c.1196T>G (p.Ile399Ser)
n.1425T>G
c.1451T>G (p.Ile484Ser)
c.752T>G (p.Ile251Ser)
2g.211702083A>GCA350442422ERBB4c.1373T>C (p.Ile458Thr)
c.1295T>C (p.Ile432Thr)
c.1372T>C
c.1196T>C (p.Ile399Thr)
n.1425T>C
c.1451T>C (p.Ile484Thr)
c.752T>C (p.Ile251Thr)
2g.211702083A>TCA350442423ERBB4c.1373T>A (p.Ile458Asn)
c.1295T>A (p.Ile432Asn)
c.1372T>A
c.1196T>A (p.Ile399Asn)
n.1425T>A
c.1451T>A (p.Ile484Asn)
c.752T>A (p.Ile251Asn)
2g.211702084T>ACA350442426ERBB4c.1372A>T (p.Ile458Phe)
c.1294A>T (p.Ile432Phe)
c.1371A>T
c.1195A>T (p.Ile399Phe)
n.1424A>T
c.1450A>T (p.Ile484Phe)
c.751A>T (p.Ile251Phe)
dbSNP
2g.211702084T>CCA350442425ERBB4c.1372A>G (p.Ile458Val)
c.1294A>G (p.Ile432Val)
c.1371A>G
c.1195A>G (p.Ile399Val)
n.1424A>G
c.1450A>G (p.Ile484Val)
c.751A>G (p.Ile251Val)
gnomAD v4
2g.211702084T>GCA350442424ERBB4c.1372A>C (p.Ile458Leu)
c.1294A>C (p.Ile432Leu)
c.1371A>C
c.1195A>C (p.Ile399Leu)
n.1424A>C
c.1450A>C (p.Ile484Leu)
c.751A>C (p.Ile251Leu)
2g.211702085delCA2577232941ERBB4c.1371del (p.Asn457LysfsTer29)
c.1293del (p.Asn431LysfsTer29)
c.1370del
c.1194del (p.Asn398LysfsTer29)
n.1423del
c.1449del (p.Asn483LysfsTer29)
c.750del (p.Asn250LysfsTer29)
2g.211702085G>ACA2088145ERBB4c.1371C>T (p.Asn457=)
c.1293C>T (p.Asn431=)
c.1370C>T
c.1194C>T (p.Asn398=)
n.1423C>T
c.1449C>T (p.Asn483=)
c.750C>T (p.Asn250=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.211702085G>CCA350442427ERBB4c.1371C>G (p.Asn457Lys)
c.1293C>G (p.Asn431Lys)
c.1370C>G
c.1194C>G (p.Asn398Lys)
n.1423C>G
c.1449C>G (p.Asn483Lys)
c.750C>G (p.Asn250Lys)
2g.211702085G=CA1325614784ERBB4c.1371C= (p.Asn457=)
c.1293C= (p.Asn431=)
c.1370C=
c.1194C= (p.Asn398=)
n.1423C=
c.1449C= (p.Asn483=)
c.750C= (p.Asn250=)
2g.211702085G>TCA350442428ERBB4c.1371C>A (p.Asn457Lys)
c.1293C>A (p.Asn431Lys)
c.1370C>A
c.1194C>A (p.Asn398Lys)
n.1423C>A
c.1449C>A (p.Asn483Lys)
c.750C>A (p.Asn250Lys)
2g.211702086T>ACA350442429ERBB4c.1370A>T (p.Asn457Ile)
c.1292A>T (p.Asn431Ile)
c.1369A>T
c.1193A>T (p.Asn398Ile)
n.1422A>T
c.1448A>T (p.Asn483Ile)
c.749A>T (p.Asn250Ile)
2g.211702086T>CCA350442430ERBB4c.1370A>G (p.Asn457Ser)
c.1292A>G (p.Asn431Ser)
c.1369A>G
c.1193A>G (p.Asn398Ser)
n.1422A>G
c.1448A>G (p.Asn483Ser)
c.749A>G (p.Asn250Ser)
gnomAD v4
2g.211702086T>GCA350442431ERBB4c.1370A>C (p.Asn457Thr)
c.1292A>C (p.Asn431Thr)
c.1369A>C
c.1193A>C (p.Asn398Thr)
n.1422A>C
c.1448A>C (p.Asn483Thr)
c.749A>C (p.Asn250Thr)
2g.211702087T>ACA350442432ERBB4c.1369A>T (p.Asn457Tyr)
c.1291A>T (p.Asn431Tyr)
c.1368A>T
c.1192A>T (p.Asn398Tyr)
n.1421A>T
c.1447A>T (p.Asn483Tyr)
c.748A>T (p.Asn250Tyr)
2g.211702087T>CCA350442433ERBB4c.1369A>G (p.Asn457Asp)
c.1291A>G (p.Asn431Asp)
c.1368A>G
c.1192A>G (p.Asn398Asp)
n.1421A>G
c.1447A>G (p.Asn483Asp)
c.748A>G (p.Asn250Asp)
2g.211702087T>GCA350442434ERBB4c.1369A>C (p.Asn457His)
c.1291A>C (p.Asn431His)
c.1368A>C
c.1192A>C (p.Asn398His)
n.1421A>C
c.1447A>C (p.Asn483His)
c.748A>C (p.Asn250His)
2g.211702088T>ACA431130928ERBB4c.1368A>T (p.Gly456=)
c.1290A>T (p.Gly430=)
c.1367A>T
c.1191A>T (p.Gly397=)
n.1420A>T
c.1446A>T (p.Gly482=)
c.747A>T (p.Gly249=)
2g.211702088T>CCA431130930ERBB4c.1368A>G (p.Gly456=)
c.1290A>G (p.Gly430=)
c.1367A>G
c.1191A>G (p.Gly397=)
n.1420A>G
c.1446A>G (p.Gly482=)
c.747A>G (p.Gly249=)
2g.211702088T>GCA431130932ERBB4c.1368A>C (p.Gly456=)
c.1290A>C (p.Gly430=)
c.1367A>C
c.1191A>C (p.Gly397=)
n.1420A>C
c.1446A>C (p.Gly482=)
c.747A>C (p.Gly249=)
2g.211702089C>ACA350442435ERBB4c.1367G>T (p.Gly456Val)
c.1289G>T (p.Gly430Val)
c.1366G>T
c.1190G>T (p.Gly397Val)
n.1419G>T
c.1445G>T (p.Gly482Val)
c.746G>T (p.Gly249Val)
2g.211702089C>GCA350442436ERBB4c.1367G>C (p.Gly456Ala)
c.1289G>C (p.Gly430Ala)
c.1366G>C
c.1190G>C (p.Gly397Ala)
n.1419G>C
c.1445G>C (p.Gly482Ala)
c.746G>C (p.Gly249Ala)
dbSNP
2g.211702089C>TCA350442437ERBB4c.1367G>A (p.Gly456Glu)
c.1289G>A (p.Gly430Glu)
c.1366G>A
c.1190G>A (p.Gly397Glu)
n.1419G>A
c.1445G>A (p.Gly482Glu)
c.746G>A (p.Gly249Glu)
COSMIC COSMIC
2g.211702090C>ACA350442440ERBB4c.1366G>T (p.Gly456Ter)
c.1288G>T (p.Gly430Ter)
c.1365G>T
c.1189G>T (p.Gly397Ter)
n.1418G>T
c.1444G>T (p.Gly482Ter)
c.745G>T (p.Gly249Ter)
2g.211702090C>GCA350442439ERBB4c.1366G>C (p.Gly456Arg)
c.1288G>C (p.Gly430Arg)
c.1365G>C
c.1189G>C (p.Gly397Arg)
n.1418G>C
c.1444G>C (p.Gly482Arg)
c.745G>C (p.Gly249Arg)
dbSNP
2g.211702090C>TCA350442438ERBB4c.1366G>A (p.Gly456Arg)
c.1288G>A (p.Gly430Arg)
c.1365G>A
c.1189G>A (p.Gly397Arg)
n.1418G>A
c.1444G>A (p.Gly482Arg)
c.745G>A (p.Gly249Arg)
2g.211702091T>ACA431130939ERBB4c.1365A>T (p.Ala455=)
c.1287A>T (p.Ala429=)
c.1364A>T
c.1188A>T (p.Ala396=)
n.1417A>T
c.1443A>T (p.Ala481=)
c.744A>T (p.Ala248=)
COSMIC COSMIC
2g.211702091T>CCA431130941ERBB4c.1365A>G (p.Ala455=)
c.1287A>G (p.Ala429=)
c.1364A>G
c.1188A>G (p.Ala396=)
n.1417A>G
c.1443A>G (p.Ala481=)
c.744A>G (p.Ala248=)
dbSNP gnomAD v4
2g.211702091T>GCA431130943ERBB4c.1365A>C (p.Ala455=)
c.1287A>C (p.Ala429=)
c.1364A>C
c.1188A>C (p.Ala396=)
n.1417A>C
c.1443A>C (p.Ala481=)
c.744A>C (p.Ala248=)
2g.211702092G>ACA350442441ERBB4c.1364C>T (p.Ala455Val)
c.1286C>T (p.Ala429Val)
c.1363C>T
c.1187C>T (p.Ala396Val)
n.1416C>T
c.1442C>T (p.Ala481Val)
c.743C>T (p.Ala248Val)
dbSNP gnomAD v2
2g.211702092G>CCA350442442ERBB4c.1364C>G (p.Ala455Gly)
c.1286C>G (p.Ala429Gly)
c.1363C>G
c.1187C>G (p.Ala396Gly)
n.1416C>G
c.1442C>G (p.Ala481Gly)
c.743C>G (p.Ala248Gly)
ClinVar dbSNP gnomAD v4
2g.211702092G=CA1325614785ERBB4c.1364C= (p.Ala455=)
c.1286C= (p.Ala429=)
c.1363C=
c.1187C= (p.Ala396=)
n.1416C=
c.1442C= (p.Ala481=)
c.743C= (p.Ala248=)
2g.211702092G>TCA350442443ERBB4c.1364C>A (p.Ala455Glu)
c.1286C>A (p.Ala429Glu)
c.1363C>A
c.1187C>A (p.Ala396Glu)
n.1416C>A
c.1442C>A (p.Ala481Glu)
c.743C>A (p.Ala248Glu)
2g.211702093C>ACA350442444ERBB4c.1363G>T (p.Ala455Ser)
c.1285G>T (p.Ala429Ser)
c.1362G>T
c.1186G>T (p.Ala396Ser)
n.1415G>T
c.1441G>T (p.Ala481Ser)
c.742G>T (p.Ala248Ser)
dbSNP gnomAD v2 gnomAD v4
2g.211702093C=CA1325614786ERBB4c.1363G= (p.Ala455=)
c.1285G= (p.Ala429=)
c.1362G=
c.1186G= (p.Ala396=)
n.1415G=
c.1441G= (p.Ala481=)
c.742G= (p.Ala248=)
2g.211702093C>GCA350442445ERBB4c.1363G>C (p.Ala455Pro)
c.1285G>C (p.Ala429Pro)
c.1362G>C
c.1186G>C (p.Ala396Pro)
n.1415G>C
c.1441G>C (p.Ala481Pro)
c.742G>C (p.Ala248Pro)
dbSNP
2g.211702093C>TCA2088146ERBB4c.1363G>A (p.Ala455Thr)
c.1285G>A (p.Ala429Thr)
c.1362G>A
c.1186G>A (p.Ala396Thr)
n.1415G>A
c.1441G>A (p.Ala481Thr)
c.742G>A (p.Ala248Thr)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.211702094G>ACA2088147ERBB4c.1362C>T (p.Ser454=)
c.1284C>T (p.Ser428=)
c.1361C>T
c.1185C>T (p.Ser395=)
n.1414C>T
c.1440C>T (p.Ser480=)
c.741C>T (p.Ser247=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.211702094G>CCA350442446ERBB4c.1362C>G (p.Ser454Arg)
c.1284C>G (p.Ser428Arg)
c.1361C>G
c.1185C>G (p.Ser395Arg)
n.1414C>G
c.1440C>G (p.Ser480Arg)
c.741C>G (p.Ser247Arg)
dbSNP
2g.211702094G=CA1325614787ERBB4c.1362C= (p.Ser454=)
c.1284C= (p.Ser428=)
c.1361C=
c.1185C= (p.Ser395=)
n.1414C=
c.1440C= (p.Ser480=)
c.741C= (p.Ser247=)
2g.211702094G>TCA350442447ERBB4c.1362C>A (p.Ser454Arg)
c.1284C>A (p.Ser428Arg)
c.1361C>A
c.1185C>A (p.Ser395Arg)
n.1414C>A
c.1440C>A (p.Ser480Arg)
c.741C>A (p.Ser247Arg)
2g.211702095C>ACA350442448ERBB4c.1361G>T (p.Ser454Ile)
c.1283G>T (p.Ser428Ile)
c.1360G>T
c.1184G>T (p.Ser395Ile)
n.1413G>T
c.1439G>T (p.Ser480Ile)
c.740G>T (p.Ser247Ile)
dbSNP
2g.211702095C=CA1325614788ERBB4c.1361G= (p.Ser454=)
c.1283G= (p.Ser428=)
c.1360G=
c.1184G= (p.Ser395=)
n.1413G=
c.1439G= (p.Ser480=)
c.740G= (p.Ser247=)
2g.211702095C>GCA350442449ERBB4c.1361G>C (p.Ser454Thr)
c.1283G>C (p.Ser428Thr)
c.1360G>C
c.1184G>C (p.Ser395Thr)
n.1413G>C
c.1439G>C (p.Ser480Thr)
c.740G>C (p.Ser247Thr)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.211702095C>TCA350442450ERBB4c.1361G>A (p.Ser454Asn)
c.1283G>A (p.Ser428Asn)
c.1360G>A
c.1184G>A (p.Ser395Asn)
n.1413G>A
c.1439G>A (p.Ser480Asn)
c.740G>A (p.Ser247Asn)
dbSNP
2g.211702096T>ACA350442453ERBB4c.1360A>T (p.Ser454Cys)
c.1282A>T (p.Ser428Cys)
c.1359A>T
c.1183A>T (p.Ser395Cys)
n.1412A>T
c.1438A>T (p.Ser480Cys)
c.739A>T (p.Ser247Cys)
2g.211702096T>CCA350442452ERBB4c.1360A>G (p.Ser454Gly)
c.1282A>G (p.Ser428Gly)
c.1359A>G
c.1183A>G (p.Ser395Gly)
n.1412A>G
c.1438A>G (p.Ser480Gly)
c.739A>G (p.Ser247Gly)
2g.211702096T>GCA350442451ERBB4c.1360A>C (p.Ser454Arg)
c.1282A>C (p.Ser428Arg)
c.1359A>C
c.1183A>C (p.Ser395Arg)
n.1412A>C
c.1438A>C (p.Ser480Arg)
c.739A>C (p.Ser247Arg)
2g.211702097G>ACA431130977ERBB4c.1359C>T (p.Ile453=)
c.1281C>T (p.Ile427=)
c.1358C>T
c.1182C>T (p.Ile394=)
n.1411C>T
c.1437C>T (p.Ile479=)
c.738C>T (p.Ile246=)
dbSNP
2g.211702097G>CCA350442454ERBB4c.1359C>G (p.Ile453Met)
c.1281C>G (p.Ile427Met)
c.1358C>G
c.1182C>G (p.Ile394Met)
n.1411C>G
c.1437C>G (p.Ile479Met)
c.738C>G (p.Ile246Met)
2g.211702097G>TCA431130978ERBB4c.1359C>A (p.Ile453=)
c.1281C>A (p.Ile427=)
c.1358C>A
c.1182C>A (p.Ile394=)
n.1411C>A
c.1437C>A (p.Ile479=)
c.738C>A (p.Ile246=)
2g.211702098A>CCA350442456ERBB4c.1358T>G (p.Ile453Ser)
c.1280T>G (p.Ile427Ser)
c.1357T>G
c.1181T>G (p.Ile394Ser)
n.1410T>G
c.1436T>G (p.Ile479Ser)
c.737T>G (p.Ile246Ser)
2g.211702098A>GCA350442455ERBB4c.1358T>C (p.Ile453Thr)
c.1280T>C (p.Ile427Thr)
c.1357T>C
c.1181T>C (p.Ile394Thr)
n.1410T>C
c.1436T>C (p.Ile479Thr)
c.737T>C (p.Ile246Thr)
2g.211702098A>TCA350442457ERBB4c.1358T>A (p.Ile453Asn)
c.1280T>A (p.Ile427Asn)
c.1357T>A
c.1181T>A (p.Ile394Asn)
n.1410T>A
c.1436T>A (p.Ile479Asn)
c.737T>A (p.Ile246Asn)
dbSNP
2g.211702099T>ACA2088148ERBB4c.1357A>T (p.Ile453Phe)
c.1279A>T (p.Ile427Phe)
c.1356A>T
c.1180A>T (p.Ile394Phe)
n.1409A>T
c.1435A>T (p.Ile479Phe)
c.736A>T (p.Ile246Phe)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.211702099T>CCA350442458ERBB4c.1357A>G (p.Ile453Val)
c.1279A>G (p.Ile427Val)
c.1356A>G
c.1180A>G (p.Ile394Val)
n.1409A>G
c.1435A>G (p.Ile479Val)
c.736A>G (p.Ile246Val)
2g.211702099T>GCA350442459ERBB4c.1357A>C (p.Ile453Leu)
c.1279A>C (p.Ile427Leu)
c.1356A>C
c.1180A>C (p.Ile394Leu)
n.1409A>C
c.1435A>C (p.Ile479Leu)
c.736A>C (p.Ile246Leu)
2g.211702099T=CA1325614789ERBB4c.1357A= (p.Ile453=)
c.1279A= (p.Ile427=)
c.1356A=
c.1180A= (p.Ile394=)
n.1409A=
c.1435A= (p.Ile479=)
c.736A= (p.Ile246=)
2g.211702100T>ACA350442460ERBB4c.1356A>T (p.Glu452Asp)
c.1278A>T (p.Glu426Asp)
c.1355A>T
c.1179A>T (p.Glu393Asp)
n.1408A>T
c.1434A>T (p.Glu478Asp)
c.735A>T (p.Glu245Asp)
dbSNP
2g.211702100T>CCA431130987ERBB4c.1356A>G (p.Glu452=)
c.1278A>G (p.Glu426=)
c.1355A>G
c.1179A>G (p.Glu393=)
n.1408A>G
c.1434A>G (p.Glu478=)
c.735A>G (p.Glu245=)
2g.211702100T>GCA350442461ERBB4c.1356A>C (p.Glu452Asp)
c.1278A>C (p.Glu426Asp)
c.1355A>C
c.1179A>C (p.Glu393Asp)
n.1408A>C
c.1434A>C (p.Glu478Asp)
c.735A>C (p.Glu245Asp)
2g.211702100T=CA1325614790ERBB4c.1356A= (p.Glu452=)
c.1278A= (p.Glu426=)
c.1355A=
c.1179A= (p.Glu393=)
n.1408A=
c.1434A= (p.Glu478=)
c.735A= (p.Glu245=)
2g.211702101T>ACA350442462ERBB4c.1355A>T (p.Glu452Val)
c.1277A>T (p.Glu426Val)
c.1354A>T
c.1178A>T (p.Glu393Val)
n.1407A>T
c.1433A>T (p.Glu478Val)
c.734A>T (p.Glu245Val)
2g.211702101T>CCA350442463ERBB4c.1355A>G (p.Glu452Gly)
c.1277A>G (p.Glu426Gly)
c.1354A>G
c.1178A>G (p.Glu393Gly)
n.1407A>G
c.1433A>G (p.Glu478Gly)
c.734A>G (p.Glu245Gly)
2g.211702101T>GCA350442464ERBB4c.1355A>C (p.Glu452Ala)
c.1277A>C (p.Glu426Ala)
c.1354A>C
c.1178A>C (p.Glu393Ala)
n.1407A>C
c.1433A>C (p.Glu478Ala)
c.734A>C (p.Glu245Ala)
2g.211702102C>ACA350442465ERBB4c.1354G>T (p.Glu452Ter)
c.1276G>T (p.Glu426Ter)
c.1353G>T
c.1177G>T (p.Glu393Ter)
n.1406G>T
c.1432G>T (p.Glu478Ter)
c.733G>T (p.Glu245Ter)
dbSNP
2g.211702102C=CA1325614791ERBB4c.1354G= (p.Glu452=)
c.1276G= (p.Glu426=)
c.1353G=
c.1177G= (p.Glu393=)
n.1406G=
c.1432G= (p.Glu478=)
c.733G= (p.Glu245=)
2g.211702102C>GCA350442466ERBB4c.1354G>C (p.Glu452Gln)
c.1276G>C (p.Glu426Gln)
c.1353G>C
c.1177G>C (p.Glu393Gln)
n.1406G>C
c.1432G>C (p.Glu478Gln)
c.733G>C (p.Glu245Gln)
2g.211702102C>TCA16602262ERBB4c.1354G>A (p.Glu452Lys)
c.1276G>A (p.Glu426Lys)
c.1353G>A
c.1177G>A (p.Glu393Lys)
n.1406G>A
c.1432G>A (p.Glu478Lys)
c.733G>A (p.Glu245Lys)
ClinVar dbSNP gnomAD v4 COSMIC
2g.211702103C>ACA350442468ERBB4c.1353G>T (p.Lys451Asn)
c.1275G>T (p.Lys425Asn)
c.1352G>T
c.1176G>T (p.Lys392Asn)
n.1405G>T
c.1431G>T (p.Lys477Asn)
c.732G>T (p.Lys244Asn)
2g.211702103C>GCA350442467ERBB4c.1353G>C (p.Lys451Asn)
c.1275G>C (p.Lys425Asn)
c.1352G>C
c.1176G>C (p.Lys392Asn)
n.1405G>C
c.1431G>C (p.Lys477Asn)
c.732G>C (p.Lys244Asn)
2g.211702103C>TCA431130996ERBB4c.1353G>A (p.Lys451=)
c.1275G>A (p.Lys425=)
c.1352G>A
c.1176G>A (p.Lys392=)
n.1405G>A
c.1431G>A (p.Lys477=)
c.732G>A (p.Lys244=)
dbSNP COSMIC COSMIC
2g.211702104T>ACA350442469ERBB4c.1352A>T (p.Lys451Met)
c.1274A>T (p.Lys425Met)
c.1351A>T
c.1175A>T (p.Lys392Met)
n.1404A>T
c.1430A>T (p.Lys477Met)
c.731A>T (p.Lys244Met)
2g.211702104T>CCA350442470ERBB4c.1352A>G (p.Lys451Arg)
c.1274A>G (p.Lys425Arg)
c.1351A>G
c.1175A>G (p.Lys392Arg)
n.1404A>G
c.1430A>G (p.Lys477Arg)
c.731A>G (p.Lys244Arg)
gnomAD v4
2g.211702104T>GCA350442471ERBB4c.1352A>C (p.Lys451Thr)
c.1274A>C (p.Lys425Thr)
c.1351A>C
c.1175A>C (p.Lys392Thr)
n.1404A>C
c.1430A>C (p.Lys477Thr)
c.731A>C (p.Lys244Thr)
2g.211702105T>ACA350442472ERBB4c.1351A>T (p.Lys451Ter)
c.1273A>T (p.Lys425Ter)
c.1350A>T
c.1174A>T (p.Lys392Ter)
n.1403A>T
c.1429A>T (p.Lys477Ter)
c.730A>T (p.Lys244Ter)
2g.211702105T>CCA350442473ERBB4c.1351A>G (p.Lys451Glu)
c.1273A>G (p.Lys425Glu)
c.1350A>G
c.1174A>G (p.Lys392Glu)
n.1403A>G
c.1429A>G (p.Lys477Glu)
c.730A>G (p.Lys244Glu)
2g.211702105T>GCA350442474ERBB4c.1351A>C (p.Lys451Gln)
c.1273A>C (p.Lys425Gln)
c.1350A>C
c.1174A>C (p.Lys392Gln)
n.1403A>C
c.1429A>C (p.Lys477Gln)
c.730A>C (p.Lys244Gln)

Number of alleles fetched