Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.177095545_177095559dupCA564898818FGFR4c.1643_1657dup (p.Cys552_Ala553insValIleValGluCys)
c.1523_1537dup (p.Cys512_Ala513insValIleValGluCys)
c.1439_1453dup (p.Cys484_Ala485insValIleValGluCys)
n.629_643dup
c.537_551dup
c.1736_1750dup (p.Cys583_Ala584insValIleValGluCys)
c.1325_1339dup (p.Cys446_Ala447insValIleValGluCys)
n.1638_1652dup
 dbSNP gnomAD v2 gnomAD v4
5g.177095553_177095559dupCA2676683373FGFR4c.1651_1657dup (p.Ala553GlyfsTer31)
c.1531_1537dup (p.Ala513GlyfsTer31)
c.1447_1453dup (p.Ala485GlyfsTer31)
n.637_643dup
c.545_551dup
c.1744_1750dup (p.Ala584GlyfsTer31)
c.1333_1339dup (p.Ala447GlyfsTer31)
n.1646_1652dup
 gnomAD v4
5g.177095553G>ACA362297023FGFR4c.1651G>A (p.Glu551Lys)
c.1531G>A (p.Glu511Lys)
c.1447G>A (p.Glu483Lys)
n.637G>A
c.545G>A
c.1744G>A (p.Glu582Lys)
c.1333G>A (p.Glu445Lys)
n.1646G>A
5g.177095553G>CCA362297026FGFR4c.1651G>C (p.Glu551Gln)
c.1531G>C (p.Glu511Gln)
c.1447G>C (p.Glu483Gln)
n.637G>C
c.545G>C
c.1744G>C (p.Glu582Gln)
c.1333G>C (p.Glu445Gln)
n.1646G>C
5g.177095553G=CA1603404301FGFR4c.1651G= (p.Glu551=)
c.1531G= (p.Glu511=)
c.1447G= (p.Glu483=)
n.637G=
c.545G=
c.1744G= (p.Glu582=)
c.1333G= (p.Glu445=)
n.1646G=
5g.177095553G>TCA362297027FGFR4c.1651G>T (p.Glu551Ter)
c.1531G>T (p.Glu511Ter)
c.1447G>T (p.Glu483Ter)
n.637G>T
c.545G>T
c.1744G>T (p.Glu582Ter)
c.1333G>T (p.Glu445Ter)
n.1646G>T
 dbSNP gnomAD v3 gnomAD v4
5g.177095554A>CCA362297028FGFR4c.1652A>C (p.Glu551Ala)
c.1532A>C (p.Glu511Ala)
c.1448A>C (p.Glu483Ala)
n.638A>C
c.546A>C
c.1745A>C (p.Glu582Ala)
c.1334A>C (p.Glu445Ala)
n.1647A>C
5g.177095554A>GCA362297030FGFR4c.1652A>G (p.Glu551Gly)
c.1532A>G (p.Glu511Gly)
c.1448A>G (p.Glu483Gly)
n.638A>G
c.546A>G
c.1745A>G (p.Glu582Gly)
c.1334A>G (p.Glu445Gly)
n.1647A>G
 gnomAD v4
5g.177095554A>TCA362297032FGFR4c.1652A>T (p.Glu551Val)
c.1532A>T (p.Glu511Val)
c.1448A>T (p.Glu483Val)
n.638A>T
c.546A>T
c.1745A>T (p.Glu582Val)
c.1334A>T (p.Glu445Val)
n.1647A>T
 gnomAD v4
5g.177095555G>ACA447725533FGFR4c.1653G>A (p.Glu551=)
c.1533G>A (p.Glu511=)
c.1449G>A (p.Glu483=)
n.639G>A
c.547G>A
c.1746G>A (p.Glu582=)
c.1335G>A (p.Glu445=)
n.1648G>A
 gnomAD v4
5g.177095555G>CCA362297034FGFR4c.1653G>C (p.Glu551Asp)
c.1533G>C (p.Glu511Asp)
c.1449G>C (p.Glu483Asp)
n.639G>C
c.547G>C
c.1746G>C (p.Glu582Asp)
c.1335G>C (p.Glu445Asp)
n.1648G>C
5g.177095555G>TCA362297035FGFR4c.1653G>T (p.Glu551Asp)
c.1533G>T (p.Glu511Asp)
c.1449G>T (p.Glu483Asp)
n.639G>T
c.547G>T
c.1746G>T (p.Glu582Asp)
c.1335G>T (p.Glu445Asp)
n.1648G>T
5g.177095556T>ACA362297037FGFR4c.1654T>A (p.Cys552Ser)
c.1534T>A (p.Cys512Ser)
c.1450T>A (p.Cys484Ser)
n.640T>A
c.548T>A
c.1747T>A (p.Cys583Ser)
c.1336T>A (p.Cys446Ser)
n.1649T>A
5g.177095556T>CCA3576507FGFR4c.1654T>C (p.Cys552Arg)
c.1534T>C (p.Cys512Arg)
c.1450T>C (p.Cys484Arg)
n.640T>C
c.548T>C
c.1747T>C (p.Cys583Arg)
c.1336T>C (p.Cys446Arg)
n.1649T>C
 dbSNP ExAC gnomAD v2 gnomAD v4
5g.177095556T>GCA362297040FGFR4c.1654T>G (p.Cys552Gly)
c.1534T>G (p.Cys512Gly)
c.1450T>G (p.Cys484Gly)
n.640T>G
c.548T>G
c.1747T>G (p.Cys583Gly)
c.1336T>G (p.Cys446Gly)
n.1649T>G
 gnomAD v4
5g.177095556T=CA1603404302FGFR4c.1654T= (p.Cys552=)
c.1534T= (p.Cys512=)
c.1450T= (p.Cys484=)
n.640T=
c.548T=
c.1747T= (p.Cys583=)
c.1336T= (p.Cys446=)
n.1649T=
5g.177095557G>ACA3576509FGFR4c.1655G>A (p.Cys552Tyr)
c.1535G>A (p.Cys512Tyr)
c.1451G>A (p.Cys484Tyr)
n.641G>A
c.549G>A
c.1748G>A (p.Cys583Tyr)
c.1337G>A (p.Cys446Tyr)
n.1650G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177095557G>CCA362297043FGFR4c.1655G>C (p.Cys552Ser)
c.1535G>C (p.Cys512Ser)
c.1451G>C (p.Cys484Ser)
n.641G>C
c.549G>C
c.1748G>C (p.Cys583Ser)
c.1337G>C (p.Cys446Ser)
n.1650G>C
5g.177095557G=CA1603404303FGFR4c.1655G= (p.Cys552=)
c.1535G= (p.Cys512=)
c.1451G= (p.Cys484=)
n.641G=
c.549G=
c.1748G= (p.Cys583=)
c.1337G= (p.Cys446=)
n.1650G=
5g.177095557G>TCA362297042FGFR4c.1655G>T (p.Cys552Phe)
c.1535G>T (p.Cys512Phe)
c.1451G>T (p.Cys484Phe)
n.641G>T
c.549G>T
c.1748G>T (p.Cys583Phe)
c.1337G>T (p.Cys446Phe)
n.1650G>T
5g.177095557_177095560delinsGCGCCA1603404304FGFR4c.1655_1658delinsGCGC (p.Cys552=)
c.1535_1538delinsGCGC (p.Cys512=)
c.1451_1454delinsGCGC (p.Cys484=)
n.641_644delinsGCGC
c.549_552delinsGCGC
c.1748_1751delinsGCGC (p.Cys583=)
c.1337_1340delinsGCGC (p.Cys446=)
n.1650_1653delinsGCGC
5g.177095558C>ACA362297047FGFR4c.1656C>A (p.Cys552Ter)
c.1536C>A (p.Cys512Ter)
c.1452C>A (p.Cys484Ter)
n.642C>A
c.550C>A
c.1749C>A (p.Cys583Ter)
c.1338C>A (p.Cys446Ter)
n.1651C>A
 dbSNP gnomAD v4
5g.177095558C=CA1603404305FGFR4c.1656C= (p.Cys552=)
c.1536C= (p.Cys512=)
c.1452C= (p.Cys484=)
n.642C=
c.550C=
c.1749C= (p.Cys583=)
c.1338C= (p.Cys446=)
n.1651C=
5g.177095558C>GCA362297049FGFR4c.1656C>G (p.Cys552Trp)
c.1536C>G (p.Cys512Trp)
c.1452C>G (p.Cys484Trp)
n.642C>G
c.550C>G
c.1749C>G (p.Cys583Trp)
c.1338C>G (p.Cys446Trp)
n.1651C>G
5g.177095558C>TCA3576510FGFR4c.1656C>T (p.Cys552=)
c.1536C>T (p.Cys512=)
c.1452C>T (p.Cys484=)
n.642C>T
c.550C>T
c.1749C>T (p.Cys583=)
c.1338C>T (p.Cys446=)
n.1651C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
5g.177095562_177095564delCA3576508FGFR4c.1660_1662del (p.Ala554del)
c.1540_1542del (p.Ala514del)
c.1456_1458del (p.Ala486del)
n.646_648del
c.554_556del
c.1753_1755del (p.Ala585del)
c.1342_1344del (p.Ala448del)
n.1655_1657del
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177095559G>ACA3576511FGFR4c.1657G>A (p.Ala553Thr)
c.1537G>A (p.Ala513Thr)
c.1453G>A (p.Ala485Thr)
n.643G>A
c.551G>A
c.1750G>A (p.Ala584Thr)
c.1339G>A (p.Ala447Thr)
n.1652G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177095559G>CCA362297053FGFR4c.1657G>C (p.Ala553Pro)
c.1537G>C (p.Ala513Pro)
c.1453G>C (p.Ala485Pro)
n.643G>C
c.551G>C
c.1750G>C (p.Ala584Pro)
c.1339G>C (p.Ala447Pro)
n.1652G>C
5g.177095559G=CA1603404306FGFR4c.1657G= (p.Ala553=)
c.1537G= (p.Ala513=)
c.1453G= (p.Ala485=)
n.643G=
c.551G=
c.1750G= (p.Ala584=)
c.1339G= (p.Ala447=)
n.1652G=
5g.177095559G>TCA362297055FGFR4c.1657G>T (p.Ala553Ser)
c.1537G>T (p.Ala513Ser)
c.1453G>T (p.Ala485Ser)
n.643G>T
c.551G>T
c.1750G>T (p.Ala584Ser)
c.1339G>T (p.Ala447Ser)
n.1652G>T
 dbSNP gnomAD v4
5g.177095560C>ACA362297056FGFR4c.1658C>A (p.Ala553Asp)
c.1538C>A (p.Ala513Asp)
c.1454C>A (p.Ala485Asp)
n.644C>A
c.552C>A
c.1751C>A (p.Ala584Asp)
c.1340C>A (p.Ala447Asp)
n.1653C>A
5g.177095560C=CA1603404307FGFR4c.1658C= (p.Ala553=)
c.1538C= (p.Ala513=)
c.1454C= (p.Ala485=)
n.644C=
c.552C=
c.1751C= (p.Ala584=)
c.1340C= (p.Ala447=)
n.1653C=
5g.177095560C>GCA362297058FGFR4c.1658C>G (p.Ala553Gly)
c.1538C>G (p.Ala513Gly)
c.1454C>G (p.Ala485Gly)
n.644C>G
c.552C>G
c.1751C>G (p.Ala584Gly)
c.1340C>G (p.Ala447Gly)
n.1653C>G
5g.177095560C>TCA132833067FGFR4c.1658C>T (p.Ala553Val)
c.1538C>T (p.Ala513Val)
c.1454C>T (p.Ala485Val)
n.644C>T
c.552C>T
c.1751C>T (p.Ala584Val)
c.1340C>T (p.Ala447Val)
n.1653C>T
 dbSNP gnomAD v4
5g.177095561dupCA2676683379FGFR4c.1659dup (p.Ala554ArgfsTer28)
c.1539dup (p.Ala514ArgfsTer28)
c.1455dup (p.Ala486ArgfsTer28)
n.645dup
c.553dup
c.1752dup (p.Ala585ArgfsTer28)
c.1341dup (p.Ala448ArgfsTer28)
n.1654dup
 gnomAD v4
5g.177095561C>ACA447725534FGFR4c.1659C>A (p.Ala553=)
c.1539C>A (p.Ala513=)
c.1455C>A (p.Ala485=)
n.645C>A
c.553C>A
c.1752C>A (p.Ala584=)
c.1341C>A (p.Ala447=)
n.1654C>A
 gnomAD v4
5g.177095561C=CA1603404308FGFR4c.1659C= (p.Ala553=)
c.1539C= (p.Ala513=)
c.1455C= (p.Ala485=)
n.645C=
c.553C=
c.1752C= (p.Ala584=)
c.1341C= (p.Ala447=)
n.1654C=
5g.177095561C>GCA447725535FGFR4c.1659C>G (p.Ala553=)
c.1539C>G (p.Ala513=)
c.1455C>G (p.Ala485=)
n.645C>G
c.553C>G
c.1752C>G (p.Ala584=)
c.1341C>G (p.Ala447=)
n.1654C>G
5g.177095561C>TCA3576512FGFR4c.1659C>T (p.Ala553=)
c.1539C>T (p.Ala513=)
c.1455C>T (p.Ala485=)
n.645C>T
c.553C>T
c.1752C>T (p.Ala584=)
c.1341C>T (p.Ala447=)
n.1654C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177095562G>ACA3576513FGFR4c.1660G>A (p.Ala554Thr)
c.1540G>A (p.Ala514Thr)
c.1456G>A (p.Ala486Thr)
n.646G>A
c.554G>A
c.1753G>A (p.Ala585Thr)
c.1342G>A (p.Ala448Thr)
n.1655G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177095562G>CCA362297064FGFR4c.1660G>C (p.Ala554Pro)
c.1540G>C (p.Ala514Pro)
c.1456G>C (p.Ala486Pro)
n.646G>C
c.554G>C
c.1753G>C (p.Ala585Pro)
c.1342G>C (p.Ala448Pro)
n.1655G>C
5g.177095562G=CA1603404309FGFR4c.1660G= (p.Ala554=)
c.1540G= (p.Ala514=)
c.1456G= (p.Ala486=)
n.646G=
c.554G=
c.1753G= (p.Ala585=)
c.1342G= (p.Ala448=)
n.1655G=
5g.177095562G>TCA362297062FGFR4c.1660G>T (p.Ala554Ser)
c.1540G>T (p.Ala514Ser)
c.1456G>T (p.Ala486Ser)
n.646G>T
c.554G>T
c.1753G>T (p.Ala585Ser)
c.1342G>T (p.Ala448Ser)
n.1655G>T
5g.177095563C>ACA362297067FGFR4c.1661C>A (p.Ala554Asp)
c.1541C>A (p.Ala514Asp)
c.1457C>A (p.Ala486Asp)
n.647C>A
c.555C>A
c.1754C>A (p.Ala585Asp)
c.1343C>A (p.Ala448Asp)
n.1656C>A
5g.177095563C>GCA362297069FGFR4c.1661C>G (p.Ala554Gly)
c.1541C>G (p.Ala514Gly)
c.1457C>G (p.Ala486Gly)
n.647C>G
c.555C>G
c.1754C>G (p.Ala585Gly)
c.1343C>G (p.Ala448Gly)
n.1656C>G
5g.177095563C>TCA362297071FGFR4c.1661C>T (p.Ala554Val)
c.1541C>T (p.Ala514Val)
c.1457C>T (p.Ala486Val)
n.647C>T
c.555C>T
c.1754C>T (p.Ala585Val)
c.1343C>T (p.Ala448Val)
n.1656C>T
5g.177095564C>ACA447725536FGFR4c.1662C>A (p.Ala554=)
c.1542C>A (p.Ala514=)
c.1458C>A (p.Ala486=)
n.648C>A
c.556C>A
c.1755C>A (p.Ala585=)
c.1344C>A (p.Ala448=)
n.1657C>A
5g.177095564C>GCA447725537FGFR4c.1662C>G (p.Ala554=)
c.1542C>G (p.Ala514=)
c.1458C>G (p.Ala486=)
n.648C>G
c.556C>G
c.1755C>G (p.Ala585=)
c.1344C>G (p.Ala448=)
n.1657C>G
5g.177095564C>TCA447725538FGFR4c.1662C>T (p.Ala554=)
c.1542C>T (p.Ala514=)
c.1458C>T (p.Ala486=)
n.648C>T
c.556C>T
c.1755C>T (p.Ala585=)
c.1344C>T (p.Ala448=)
n.1657C>T
5g.177095565A=CA1603404310FGFR4c.1663A= (p.Lys555=)
c.1543A= (p.Lys515=)
c.1459A= (p.Lys487=)
n.649A=
c.557A=
c.1756A= (p.Lys586=)
c.1345A= (p.Lys449=)
n.1658A=
5g.177095565A>CCA3576514FGFR4c.1663A>C (p.Lys555Gln)
c.1543A>C (p.Lys515Gln)
c.1459A>C (p.Lys487Gln)
n.649A>C
c.557A>C
c.1756A>C (p.Lys586Gln)
c.1345A>C (p.Lys449Gln)
n.1658A>C
 dbSNP ExAC gnomAD v2 gnomAD v4
5g.177095565A>GCA132833083FGFR4c.1663A>G (p.Lys555Glu)
c.1543A>G (p.Lys515Glu)
c.1459A>G (p.Lys487Glu)
n.649A>G
c.557A>G
c.1756A>G (p.Lys586Glu)
c.1345A>G (p.Lys449Glu)
n.1658A>G
 dbSNP gnomAD v3 gnomAD v4
5g.177095565A>TCA362297074FGFR4c.1663A>T (p.Lys555Ter)
c.1543A>T (p.Lys515Ter)
c.1459A>T (p.Lys487Ter)
n.649A>T
c.557A>T
c.1756A>T (p.Lys586Ter)
c.1345A>T (p.Lys449Ter)
n.1658A>T
5g.177095566A>CCA362297076FGFR4c.1664A>C (p.Lys555Thr)
c.1544A>C (p.Lys515Thr)
c.1460A>C (p.Lys487Thr)
n.650A>C
c.558A>C
c.1757A>C (p.Lys586Thr)
c.1346A>C (p.Lys449Thr)
n.1659A>C
5g.177095566A>GCA362297078FGFR4c.1664A>G (p.Lys555Arg)
c.1544A>G (p.Lys515Arg)
c.1460A>G (p.Lys487Arg)
n.650A>G
c.558A>G
c.1757A>G (p.Lys586Arg)
c.1346A>G (p.Lys449Arg)
n.1659A>G
5g.177095566A>TCA362297080FGFR4c.1664A>T (p.Lys555Met)
c.1544A>T (p.Lys515Met)
c.1460A>T (p.Lys487Met)
n.650A>T
c.558A>T
c.1757A>T (p.Lys586Met)
c.1346A>T (p.Lys449Met)
n.1659A>T
5g.177095567G>ACA447725539FGFR4c.1665G>A (p.Lys555=)
c.1545G>A (p.Lys515=)
c.1461G>A (p.Lys487=)
n.651G>A
c.559G>A
c.1758G>A (p.Lys586=)
c.1347G>A (p.Lys449=)
n.1660G>A
 gnomAD v4 COSMIC COSMIC
5g.177095567G>CCA362297082FGFR4c.1665G>C (p.Lys555Asn)
c.1545G>C (p.Lys515Asn)
c.1461G>C (p.Lys487Asn)
n.651G>C
c.559G>C
c.1758G>C (p.Lys586Asn)
c.1347G>C (p.Lys449Asn)
n.1660G>C
 gnomAD v4
5g.177095567G>TCA362297084FGFR4c.1665G>T (p.Lys555Asn)
c.1545G>T (p.Lys515Asn)
c.1461G>T (p.Lys487Asn)
n.651G>T
c.559G>T
c.1758G>T (p.Lys586Asn)
c.1347G>T (p.Lys449Asn)
n.1660G>T
 gnomAD v4
5g.177095569delCA2676683382FGFR4c.1667del (p.Gly556GlufsTer?)
c.1547del (p.Gly516GlufsTer?)
c.1463del (p.Gly488GlufsTer?)
n.653del
c.561del
c.1760del (p.Gly587GlufsTer?)
c.1349del (p.Gly450GlufsTer?)
n.1662del
 gnomAD v4
5g.177095568G>ACA362297090FGFR4c.1666G>A (p.Gly556Arg)
c.1546G>A (p.Gly516Arg)
c.1462G>A (p.Gly488Arg)
n.652G>A
c.560G>A
c.1759G>A (p.Gly587Arg)
c.1348G>A (p.Gly450Arg)
n.1661G>A
 dbSNP gnomAD v2 gnomAD v4
5g.177095568G>CCA362297088FGFR4c.1666G>C (p.Gly556Arg)
c.1546G>C (p.Gly516Arg)
c.1462G>C (p.Gly488Arg)
n.652G>C
c.560G>C
c.1759G>C (p.Gly587Arg)
c.1348G>C (p.Gly450Arg)
n.1661G>C
5g.177095568G=CA1603404311FGFR4c.1666G= (p.Gly556=)
c.1546G= (p.Gly516=)
c.1462G= (p.Gly488=)
n.652G=
c.560G=
c.1759G= (p.Gly587=)
c.1348G= (p.Gly450=)
n.1661G=
5g.177095568G>TCA362297086FGFR4c.1666G>T (p.Gly556Ter)
c.1546G>T (p.Gly516Ter)
c.1462G>T (p.Gly488Ter)
n.652G>T
c.560G>T
c.1759G>T (p.Gly587Ter)
c.1348G>T (p.Gly450Ter)
n.1661G>T
 gnomAD v4
5g.177095569G>ACA362297091FGFR4c.1667G>A (p.Gly556Glu)
c.1547G>A (p.Gly516Glu)
c.1463G>A (p.Gly488Glu)
n.653G>A
c.561G>A
c.1760G>A (p.Gly587Glu)
c.1349G>A (p.Gly450Glu)
n.1662G>A
5g.177095569G>CCA362297093FGFR4c.1667G>C (p.Gly556Ala)
c.1547G>C (p.Gly516Ala)
c.1463G>C (p.Gly488Ala)
n.653G>C
c.561G>C
c.1760G>C (p.Gly587Ala)
c.1349G>C (p.Gly450Ala)
n.1662G>C
 gnomAD v4
5g.177095569G>TCA362297095FGFR4c.1667G>T (p.Gly556Val)
c.1547G>T (p.Gly516Val)
c.1463G>T (p.Gly488Val)
n.653G>T
c.561G>T
c.1760G>T (p.Gly587Val)
c.1349G>T (p.Gly450Val)
n.1662G>T
5g.177095570A>CCA447725542FGFR4c.1668A>C (p.Gly556=)
c.1548A>C (p.Gly516=)
c.1464A>C (p.Gly488=)
n.654A>C
c.562A>C
c.1761A>C (p.Gly587=)
c.1350A>C (p.Gly450=)
n.1663A>C
5g.177095570A>GCA447725540FGFR4c.1668A>G (p.Gly556=)
c.1548A>G (p.Gly516=)
c.1464A>G (p.Gly488=)
n.654A>G
c.562A>G
c.1761A>G (p.Gly587=)
c.1350A>G (p.Gly450=)
n.1663A>G
5g.177095570A>TCA447725541FGFR4c.1668A>T (p.Gly556=)
c.1548A>T (p.Gly516=)
c.1464A>T (p.Gly488=)
n.654A>T
c.562A>T
c.1761A>T (p.Gly587=)
c.1350A>T (p.Gly450=)
n.1663A>T
5g.177095571A>CCA362297097FGFR4c.1669A>C (p.Asn557His)
c.1549A>C (p.Asn517His)
c.1465A>C (p.Asn489His)
n.655A>C
c.563A>C
c.1762A>C (p.Asn588His)
c.1351A>C (p.Asn451His)
n.1664A>C
5g.177095571A>GCA362297099FGFR4c.1669A>G (p.Asn557Asp)
c.1549A>G (p.Asn517Asp)
c.1465A>G (p.Asn489Asp)
n.655A>G
c.563A>G
c.1762A>G (p.Asn588Asp)
c.1351A>G (p.Asn451Asp)
n.1664A>G
5g.177095571A>TCA362297101FGFR4c.1669A>T (p.Asn557Tyr)
c.1549A>T (p.Asn517Tyr)
c.1465A>T (p.Asn489Tyr)
n.655A>T
c.563A>T
c.1762A>T (p.Asn588Tyr)
c.1351A>T (p.Asn451Tyr)
n.1664A>T
5g.177095572A=CA1603404312FGFR4c.1670A= (p.Asn557=)
c.1550A= (p.Asn517=)
c.1466A= (p.Asn489=)
n.656A=
c.564A=
c.1763A= (p.Asn588=)
c.1352A= (p.Asn451=)
n.1665A=
5g.177095572A>CCA362297103FGFR4c.1670A>C (p.Asn557Thr)
c.1550A>C (p.Asn517Thr)
c.1466A>C (p.Asn489Thr)
n.656A>C
c.564A>C
c.1763A>C (p.Asn588Thr)
c.1352A>C (p.Asn451Thr)
n.1665A>C
5g.177095572A>GCA3576515FGFR4c.1670A>G (p.Asn557Ser)
c.1550A>G (p.Asn517Ser)
c.1466A>G (p.Asn489Ser)
n.656A>G
c.564A>G
c.1763A>G (p.Asn588Ser)
c.1352A>G (p.Asn451Ser)
n.1665A>G
 dbSNP ExAC gnomAD v2 gnomAD v4
5g.177095572A>TCA362297105FGFR4c.1670A>T (p.Asn557Ile)
c.1550A>T (p.Asn517Ile)
c.1466A>T (p.Asn489Ile)
n.656A>T
c.564A>T
c.1763A>T (p.Asn588Ile)
c.1352A>T (p.Asn451Ile)
n.1665A>T
5g.177095573C>ACA362297107FGFR4c.1671C>A (p.Asn557Lys)
c.1551C>A (p.Asn517Lys)
c.1467C>A (p.Asn489Lys)
n.657C>A
c.565C>A
c.1764C>A (p.Asn588Lys)
c.1353C>A (p.Asn451Lys)
n.1666C>A
 gnomAD v4
5g.177095573C>GCA362297109FGFR4c.1671C>G (p.Asn557Lys)
c.1551C>G (p.Asn517Lys)
c.1467C>G (p.Asn489Lys)
n.657C>G
c.565C>G
c.1764C>G (p.Asn588Lys)
c.1353C>G (p.Asn451Lys)
n.1666C>G
5g.177095573C>TCA447725543FGFR4c.1671C>T (p.Asn557=)
c.1551C>T (p.Asn517=)
c.1467C>T (p.Asn489=)
n.657C>T
c.565C>T
c.1764C>T (p.Asn588=)
c.1353C>T (p.Asn451=)
n.1666C>T
5g.177095574C>ACA362297111FGFR4c.1672C>A (p.Leu558Met)
c.1552C>A (p.Leu518Met)
c.1468C>A (p.Leu490Met)
n.658C>A
c.566C>A
c.1765C>A (p.Leu589Met)
c.1354C>A (p.Leu452Met)
n.1667C>A
 gnomAD v4
5g.177095574C>GCA362297112FGFR4c.1672C>G (p.Leu558Val)
c.1552C>G (p.Leu518Val)
c.1468C>G (p.Leu490Val)
n.658C>G
c.566C>G
c.1765C>G (p.Leu589Val)
c.1354C>G (p.Leu452Val)
n.1667C>G
5g.177095574C>TCA447725544FGFR4c.1672C>T (p.Leu558=)
c.1552C>T (p.Leu518=)
c.1468C>T (p.Leu490=)
n.658C>T
c.566C>T
c.1765C>T (p.Leu589=)
c.1354C>T (p.Leu452=)
n.1667C>T
5g.177095575T>ACA362297116FGFR4c.1673T>A (p.Leu558Gln)
c.1553T>A (p.Leu518Gln)
c.1469T>A (p.Leu490Gln)
n.659T>A
c.567T>A
c.1766T>A (p.Leu589Gln)
c.1355T>A (p.Leu452Gln)
n.1668T>A
5g.177095575T>CCA362297118FGFR4c.1673T>C (p.Leu558Pro)
c.1553T>C (p.Leu518Pro)
c.1469T>C (p.Leu490Pro)
n.659T>C
c.567T>C
c.1766T>C (p.Leu589Pro)
c.1355T>C (p.Leu452Pro)
n.1668T>C
5g.177095575T>GCA362297115FGFR4c.1673T>G (p.Leu558Arg)
c.1553T>G (p.Leu518Arg)
c.1469T>G (p.Leu490Arg)
n.659T>G
c.567T>G
c.1766T>G (p.Leu589Arg)
c.1355T>G (p.Leu452Arg)
n.1668T>G
5g.177095576G>ACA447725547FGFR4c.1674G>A (p.Leu558=)
c.1554G>A (p.Leu518=)
c.1470G>A (p.Leu490=)
n.660G>A
c.568G>A
c.1767G>A (p.Leu589=)
c.1356G>A (p.Leu452=)
n.1669G>A
5g.177095576G>CCA447725545FGFR4c.1674G>C (p.Leu558=)
c.1554G>C (p.Leu518=)
c.1470G>C (p.Leu490=)
n.660G>C
c.568G>C
c.1767G>C (p.Leu589=)
c.1356G>C (p.Leu452=)
n.1669G>C
5g.177095576G>TCA447725546FGFR4c.1674G>T (p.Leu558=)
c.1554G>T (p.Leu518=)
c.1470G>T (p.Leu490=)
n.660G>T
c.568G>T
c.1767G>T (p.Leu589=)
c.1356G>T (p.Leu452=)
n.1669G>T
 gnomAD v4
5g.177095577C>ACA3576516FGFR4c.1675C>A (p.Arg559=)
c.1555C>A (p.Arg519=)
c.1471C>A (p.Arg491=)
n.661C>A
c.569C>A
c.1768C>A (p.Arg590=)
c.1357C>A (p.Arg453=)
n.1670C>A
 dbSNP ExAC gnomAD v2 gnomAD v4
5g.177095577C=CA1603404313FGFR4c.1675C= (p.Arg559=)
c.1555C= (p.Arg519=)
c.1471C= (p.Arg491=)
n.661C=
c.569C=
c.1768C= (p.Arg590=)
c.1357C= (p.Arg453=)
n.1670C=
5g.177095577C>GCA362297121FGFR4c.1675C>G (p.Arg559Gly)
c.1555C>G (p.Arg519Gly)
c.1471C>G (p.Arg491Gly)
n.661C>G
c.569C>G
c.1768C>G (p.Arg590Gly)
c.1357C>G (p.Arg453Gly)
n.1670C>G
5g.177095577C>TCA362297123FGFR4c.1675C>T (p.Arg559Trp)
c.1555C>T (p.Arg519Trp)
c.1471C>T (p.Arg491Trp)
n.661C>T
c.569C>T
c.1768C>T (p.Arg590Trp)
c.1357C>T (p.Arg453Trp)
n.1670C>T
 dbSNP gnomAD v4
5g.177095578G>ACA3576517FGFR4c.1676G>A (p.Arg559Gln)
c.1556G>A (p.Arg519Gln)
c.1472G>A (p.Arg491Gln)
n.662G>A
c.570G>A
c.1769G>A (p.Arg590Gln)
c.1358G>A (p.Arg453Gln)
n.1671G>A
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC
5g.177095578G>CCA362297126FGFR4c.1676G>C (p.Arg559Pro)
c.1556G>C (p.Arg519Pro)
c.1472G>C (p.Arg491Pro)
n.662G>C
c.570G>C
c.1769G>C (p.Arg590Pro)
c.1358G>C (p.Arg453Pro)
n.1671G>C
5g.177095578G=CA1603404314FGFR4c.1676G= (p.Arg559=)
c.1556G= (p.Arg519=)
c.1472G= (p.Arg491=)
n.662G=
c.570G=
c.1769G= (p.Arg590=)
c.1358G= (p.Arg453=)
n.1671G=
5g.177095578G>TCA362297128FGFR4c.1676G>T (p.Arg559Leu)
c.1556G>T (p.Arg519Leu)
c.1472G>T (p.Arg491Leu)
n.662G>T
c.570G>T
c.1769G>T (p.Arg590Leu)
c.1358G>T (p.Arg453Leu)
n.1671G>T
 gnomAD v4
5g.177095579G>ACA447725548FGFR4c.1677G>A (p.Arg559=)
c.1557G>A (p.Arg519=)
c.1473G>A (p.Arg491=)
n.663G>A
c.571G>A
c.1770G>A (p.Arg590=)
c.1359G>A (p.Arg453=)
n.1672G>A
5g.177095579G>CCA447725549FGFR4c.1677G>C (p.Arg559=)
c.1557G>C (p.Arg519=)
c.1473G>C (p.Arg491=)
n.663G>C
c.571G>C
c.1770G>C (p.Arg590=)
c.1359G>C (p.Arg453=)
n.1672G>C
5g.177095579G>TCA447725550FGFR4c.1677G>T (p.Arg559=)
c.1557G>T (p.Arg519=)
c.1473G>T (p.Arg491=)
n.663G>T
c.571G>T
c.1770G>T (p.Arg590=)
c.1359G>T (p.Arg453=)
n.1672G>T
 gnomAD v4
5g.177095580G>ACA362297134FGFR4c.1678G>A (p.Glu560Lys)
c.1558G>A (p.Glu520Lys)
c.1474G>A (p.Glu492Lys)
c.572G>A
c.1771G>A (p.Glu591Lys)
c.1360G>A (p.Glu454Lys)
n.1673G>A
 gnomAD v4 COSMIC COSMIC
5g.177095580G>CCA362297130FGFR4c.1678G>C (p.Glu560Gln)
c.1558G>C (p.Glu520Gln)
c.1474G>C (p.Glu492Gln)
c.572G>C
c.1771G>C (p.Glu591Gln)
c.1360G>C (p.Glu454Gln)
n.1673G>C
 gnomAD v4
5g.177095580G>TCA362297131FGFR4c.1678G>T (p.Glu560Ter)
c.1558G>T (p.Glu520Ter)
c.1474G>T (p.Glu492Ter)
c.572G>T
c.1771G>T (p.Glu591Ter)
c.1360G>T (p.Glu454Ter)
n.1673G>T
 gnomAD v4
5g.177095581A>CCA362297136FGFR4c.1679A>C (p.Glu560Ala)
c.1559A>C (p.Glu520Ala)
c.1475A>C (p.Glu492Ala)
c.573A>C
c.1772A>C (p.Glu591Ala)
c.1361A>C (p.Glu454Ala)
n.1674A>C
5g.177095581A>GCA362297137FGFR4c.1679A>G (p.Glu560Gly)
c.1559A>G (p.Glu520Gly)
c.1475A>G (p.Glu492Gly)
c.573A>G
c.1772A>G (p.Glu591Gly)
c.1361A>G (p.Glu454Gly)
n.1674A>G
 dbSNP
5g.177095581A>TCA362297138FGFR4c.1679A>T (p.Glu560Val)
c.1559A>T (p.Glu520Val)
c.1475A>T (p.Glu492Val)
c.573A>T
c.1772A>T (p.Glu591Val)
c.1361A>T (p.Glu454Val)
n.1674A>T
5g.177095582G>ACA447725551FGFR4c.1680G>A (p.Glu560=)
c.1560G>A (p.Glu520=)
c.1476G>A (p.Glu492=)
c.574G>A
c.1773G>A (p.Glu591=)
c.1362G>A (p.Glu454=)
n.1675G>A
 dbSNP
5g.177095582G>CCA362297141FGFR4c.1680G>C (p.Glu560Asp)
c.1560G>C (p.Glu520Asp)
c.1476G>C (p.Glu492Asp)
c.574G>C
c.1773G>C (p.Glu591Asp)
c.1362G>C (p.Glu454Asp)
n.1675G>C
5g.177095582G>TCA362297142FGFR4c.1680G>T (p.Glu560Asp)
c.1560G>T (p.Glu520Asp)
c.1476G>T (p.Glu492Asp)
c.574G>T
c.1773G>T (p.Glu591Asp)
c.1362G>T (p.Glu454Asp)
n.1675G>T
5g.177095583T>ACA362297148FGFR4c.1681T>A (p.Phe561Ile)
c.1561T>A (p.Phe521Ile)
c.1477T>A (p.Phe493Ile)
c.575T>A
c.1774T>A (p.Phe592Ile)
c.1363T>A (p.Phe455Ile)
n.1676T>A
5g.177095583T>CCA362297144FGFR4c.1681T>C (p.Phe561Leu)
c.1561T>C (p.Phe521Leu)
c.1477T>C (p.Phe493Leu)
c.575T>C
c.1774T>C (p.Phe592Leu)
c.1363T>C (p.Phe455Leu)
n.1676T>C
 dbSNP
5g.177095583T>GCA362297146FGFR4c.1681T>G (p.Phe561Val)
c.1561T>G (p.Phe521Val)
c.1477T>G (p.Phe493Val)
c.575T>G
c.1774T>G (p.Phe592Val)
c.1363T>G (p.Phe455Val)
n.1676T>G
5g.177095583T=CA1603404315FGFR4c.1681T= (p.Phe561=)
c.1561T= (p.Phe521=)
c.1477T= (p.Phe493=)
c.575T=
c.1774T= (p.Phe592=)
c.1363T= (p.Phe455=)
n.1676T=
5g.177095584T>ACA362297151FGFR4c.1682T>A (p.Phe561Tyr)
c.1562T>A (p.Phe521Tyr)
c.1478T>A (p.Phe493Tyr)
c.576T>A
c.1775T>A (p.Phe592Tyr)
c.1364T>A (p.Phe455Tyr)
n.1677T>A
 dbSNP
5g.177095584T>CCA362297153FGFR4c.1682T>C (p.Phe561Ser)
c.1562T>C (p.Phe521Ser)
c.1478T>C (p.Phe493Ser)
c.576T>C
c.1775T>C (p.Phe592Ser)
c.1364T>C (p.Phe455Ser)
n.1677T>C
5g.177095584T>GCA362297154FGFR4c.1682T>G (p.Phe561Cys)
c.1562T>G (p.Phe521Cys)
c.1478T>G (p.Phe493Cys)
c.576T>G
c.1775T>G (p.Phe592Cys)
c.1364T>G (p.Phe455Cys)
n.1677T>G
5g.177095584T=CA1603404316FGFR4c.1682T= (p.Phe561=)
c.1562T= (p.Phe521=)
c.1478T= (p.Phe493=)
c.576T=
c.1775T= (p.Phe592=)
c.1364T= (p.Phe455=)
n.1677T=
5g.177095585C>ACA362297157FGFR4c.1683C>A (p.Phe561Leu)
c.1563C>A (p.Phe521Leu)
c.1479C>A (p.Phe493Leu)
c.577C>A
c.1776C>A (p.Phe592Leu)
c.1365C>A (p.Phe455Leu)
n.1678C>A
 gnomAD v4
5g.177095585C>GCA362297158FGFR4c.1683C>G (p.Phe561Leu)
c.1563C>G (p.Phe521Leu)
c.1479C>G (p.Phe493Leu)
c.577C>G
c.1776C>G (p.Phe592Leu)
c.1365C>G (p.Phe455Leu)
n.1678C>G
5g.177095585C>TCA447725552FGFR4c.1683C>T (p.Phe561=)
c.1563C>T (p.Phe521=)
c.1479C>T (p.Phe493=)
c.577C>T
c.1776C>T (p.Phe592=)
c.1365C>T (p.Phe455=)
n.1678C>T
5g.177095586delCA2676683388FGFR4c.1684del (p.Leu562CysfsTer?)
c.1564del (p.Leu522CysfsTer?)
c.1480del (p.Leu494CysfsTer?)
c.578del
c.1777del (p.Leu593CysfsTer?)
c.1366del (p.Leu456CysfsTer?)
n.1679del
 gnomAD v4
5g.177095586C>ACA362297159FGFR4c.1684C>A (p.Leu562Met)
c.1564C>A (p.Leu522Met)
c.1480C>A (p.Leu494Met)
c.578C>A
c.1777C>A (p.Leu593Met)
c.1366C>A (p.Leu456Met)
n.1679C>A
5g.177095586C=CA1603404317FGFR4c.1684C= (p.Leu562=)
c.1564C= (p.Leu522=)
c.1480C= (p.Leu494=)
c.578C=
c.1777C= (p.Leu593=)
c.1366C= (p.Leu456=)
n.1679C=
5g.177095586C>GCA362297160FGFR4c.1684C>G (p.Leu562Val)
c.1564C>G (p.Leu522Val)
c.1480C>G (p.Leu494Val)
c.578C>G
c.1777C>G (p.Leu593Val)
c.1366C>G (p.Leu456Val)
n.1679C>G
5g.177095586C>TCA229225FGFR4c.1684C>T (p.Leu562=)
c.1564C>T (p.Leu522=)
c.1480C>T (p.Leu494=)
c.578C>T
c.1777C>T (p.Leu593=)
c.1366C>T (p.Leu456=)
n.1679C>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
5g.177095587T>ACA362297161FGFR4c.1685T>A (p.Leu562Gln)
c.1565T>A (p.Leu522Gln)
c.1481T>A (p.Leu494Gln)
c.579T>A
c.1778T>A (p.Leu593Gln)
c.1367T>A (p.Leu456Gln)
n.1680T>A
5g.177095587T>CCA362297162FGFR4c.1685T>C (p.Leu562Pro)
c.1565T>C (p.Leu522Pro)
c.1481T>C (p.Leu494Pro)
c.579T>C
c.1778T>C (p.Leu593Pro)
c.1367T>C (p.Leu456Pro)
n.1680T>C
5g.177095587T>GCA362297163FGFR4c.1685T>G (p.Leu562Arg)
c.1565T>G (p.Leu522Arg)
c.1481T>G (p.Leu494Arg)
c.579T>G
c.1778T>G (p.Leu593Arg)
c.1367T>G (p.Leu456Arg)
n.1680T>G
5g.177095588G>ACA447725553FGFR4c.1686G>A (p.Leu562=)
c.1566G>A (p.Leu522=)
c.1482G>A (p.Leu494=)
c.580G>A
c.1779G>A (p.Leu593=)
c.1368G>A (p.Leu456=)
n.1681G>A
 dbSNP gnomAD v4
5g.177095588G>CCA447725554FGFR4c.1686G>C (p.Leu562=)
c.1566G>C (p.Leu522=)
c.1482G>C (p.Leu494=)
c.580G>C
c.1779G>C (p.Leu593=)
c.1368G>C (p.Leu456=)
n.1681G>C
5g.177095588G>TCA447725555FGFR4c.1686G>T (p.Leu562=)
c.1566G>T (p.Leu522=)
c.1482G>T (p.Leu494=)
c.580G>T
c.1779G>T (p.Leu593=)
c.1368G>T (p.Leu456=)
n.1681G>T
5g.177095589C>ACA447725556FGFR4c.1687C>A (p.Arg563=)
c.1567C>A (p.Arg523=)
c.1483C>A (p.Arg495=)
c.581C>A
c.1780C>A (p.Arg594=)
c.1369C>A (p.Arg457=)
n.1682C>A
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.177095589C=CA1603404318FGFR4c.1687C= (p.Arg563=)
c.1567C= (p.Arg523=)
c.1483C= (p.Arg495=)
c.581C=
c.1780C= (p.Arg594=)
c.1369C= (p.Arg457=)
n.1682C=
5g.177095589C>GCA362297164FGFR4c.1687C>G (p.Arg563Gly)
c.1567C>G (p.Arg523Gly)
c.1483C>G (p.Arg495Gly)
c.581C>G
c.1780C>G (p.Arg594Gly)
c.1369C>G (p.Arg457Gly)
n.1682C>G
5g.177095589C>TCA3576518FGFR4c.1687C>T (p.Arg563Trp)
c.1567C>T (p.Arg523Trp)
c.1483C>T (p.Arg495Trp)
c.581C>T
c.1780C>T (p.Arg594Trp)
c.1369C>T (p.Arg457Trp)
n.1682C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
5g.177095590G>ACA3576519FGFR4c.1688G>A (p.Arg563Gln)
c.1568G>A (p.Arg523Gln)
c.1484G>A (p.Arg495Gln)
c.582G>A
c.1781G>A (p.Arg594Gln)
c.1370G>A (p.Arg457Gln)
n.1683G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177095590G>CCA362297166FGFR4c.1688G>C (p.Arg563Pro)
c.1568G>C (p.Arg523Pro)
c.1484G>C (p.Arg495Pro)
c.582G>C
c.1781G>C (p.Arg594Pro)
c.1370G>C (p.Arg457Pro)
n.1683G>C
5g.177095590G=CA1603404319FGFR4c.1688G= (p.Arg563=)
c.1568G= (p.Arg523=)
c.1484G= (p.Arg495=)
c.582G=
c.1781G= (p.Arg594=)
c.1370G= (p.Arg457=)
n.1683G=
5g.177095590G>TCA362297165FGFR4c.1688G>T (p.Arg563Leu)
c.1568G>T (p.Arg523Leu)
c.1484G>T (p.Arg495Leu)
c.582G>T
c.1781G>T (p.Arg594Leu)
c.1370G>T (p.Arg457Leu)
n.1683G>T
 gnomAD v4
5g.177095592delCA2676683392FGFR4c.1690del (p.Ala564ProfsTer?)
c.1570del (p.Ala524ProfsTer?)
c.1486del (p.Ala496ProfsTer?)
c.584del
c.1783del (p.Ala595ProfsTer?)
c.1372del (p.Ala458ProfsTer?)
n.1685del
 gnomAD v4
5g.177095591G>ACA447725557FGFR4c.1689G>A (p.Arg563=)
c.1569G>A (p.Arg523=)
c.1485G>A (p.Arg495=)
c.583G>A
c.1782G>A (p.Arg594=)
c.1371G>A (p.Arg457=)
n.1684G>A
5g.177095591G>CCA447725558FGFR4c.1689G>C (p.Arg563=)
c.1569G>C (p.Arg523=)
c.1485G>C (p.Arg495=)
c.583G>C
c.1782G>C (p.Arg594=)
c.1371G>C (p.Arg457=)
n.1684G>C
5g.177095591G=CA1603404320FGFR4c.1689G= (p.Arg563=)
c.1569G= (p.Arg523=)
c.1485G= (p.Arg495=)
c.583G=
c.1782G= (p.Arg594=)
c.1371G= (p.Arg457=)
n.1684G=
5g.177095591G>TCA447725559FGFR4c.1689G>T (p.Arg563=)
c.1569G>T (p.Arg523=)
c.1485G>T (p.Arg495=)
c.583G>T
c.1782G>T (p.Arg594=)
c.1371G>T (p.Arg457=)
n.1684G>T
 dbSNP gnomAD v2
5g.177095592G>ACA362297167FGFR4c.1690G>A (p.Ala564Thr)
c.1570G>A (p.Ala524Thr)
c.1486G>A (p.Ala496Thr)
c.584G>A
c.1783G>A (p.Ala595Thr)
c.1372G>A (p.Ala458Thr)
n.1685G>A
5g.177095592G>CCA362297168FGFR4c.1690G>C (p.Ala564Pro)
c.1570G>C (p.Ala524Pro)
c.1486G>C (p.Ala496Pro)
c.584G>C
c.1783G>C (p.Ala595Pro)
c.1372G>C (p.Ala458Pro)
n.1685G>C
5g.177095592G>TCA362297169FGFR4c.1690G>T (p.Ala564Ser)
c.1570G>T (p.Ala524Ser)
c.1486G>T (p.Ala496Ser)
c.584G>T
c.1783G>T (p.Ala595Ser)
c.1372G>T (p.Ala458Ser)
n.1685G>T
 gnomAD v4
5g.177095592_177095593delinsGCCA1603404321FGFR4c.1690_1691delinsGC (p.Ala564=)
c.1570_1571delinsGC (p.Ala524=)
c.1486_1487delinsGC (p.Ala496=)
c.584_585delinsGC
c.1783_1784delinsGC (p.Ala595=)
c.1372_1373delinsGC (p.Ala458=)
n.1685_1686delinsGC
5g.177095631_177095632insAGCCCGGCGCCCCCCAGGCCCCGACCTCAGCCCCGACGGTCCA2676683394FGFR4c.1729_1730insAGCCCGGCGCCCCCCAGGCCCCGACCTCAGCCCCGACGGTC (p.Pro577GlnfsTer?)
c.1609_1610insAGCCCGGCGCCCCCCAGGCCCCGACCTCAGCCCCGACGGTC (p.Pro537GlnfsTer?)
c.1525_1526insAGCCCGGCGCCCCCCAGGCCCCGACCTCAGCCCCGACGGTC (p.Pro509GlnfsTer?)
c.623_624insAGCCCGGCGCCCCCCAGGCCCCGACCTCAGCCCCGACGGTC
c.1822_1823insAGCCCGGCGCCCCCCAGGCCCCGACCTCAGCCCCGACGGTC (p.Pro608GlnfsTer?)
c.1411_1412insAGCCCGGCGCCCCCCAGGCCCCGACCTCAGCCCCGACGGTC (p.Pro471GlnfsTer?)
n.1724_1725insAGCCCGGCGCCCCCCAGGCCCCGACCTCAGCCCCGACGGTC
 gnomAD v4
5g.177095593C>ACA362297170FGFR4c.1691C>A (p.Ala564Asp)
c.1571C>A (p.Ala524Asp)
c.1487C>A (p.Ala496Asp)
c.585C>A
c.1784C>A (p.Ala595Asp)
c.1373C>A (p.Ala458Asp)
n.1686C>A
5g.177095593C>GCA362297171FGFR4c.1691C>G (p.Ala564Gly)
c.1571C>G (p.Ala524Gly)
c.1487C>G (p.Ala496Gly)
c.585C>G
c.1784C>G (p.Ala595Gly)
c.1373C>G (p.Ala458Gly)
n.1686C>G
5g.177095593C>TCA362297172FGFR4c.1691C>T (p.Ala564Val)
c.1571C>T (p.Ala524Val)
c.1487C>T (p.Ala496Val)
c.585C>T
c.1784C>T (p.Ala595Val)
c.1373C>T (p.Ala458Val)
n.1686C>T
 dbSNP gnomAD v4
5g.177095595delCA808060491FGFR4c.1693del (p.Arg565GlyfsTer?)
c.1573del (p.Arg525GlyfsTer?)
c.1489del (p.Arg497GlyfsTer?)
c.587del
c.1786del (p.Arg596GlyfsTer?)
c.1375del (p.Arg459GlyfsTer?)
n.1688del
 dbSNP gnomAD v3 gnomAD v4
5g.177095594C>ACA447725560FGFR4c.1692C>A (p.Ala564=)
c.1572C>A (p.Ala524=)
c.1488C>A (p.Ala496=)
c.586C>A
c.1785C>A (p.Ala595=)
c.1374C>A (p.Ala458=)
n.1687C>A
 gnomAD v4
5g.177095594C>GCA447725561FGFR4c.1692C>G (p.Ala564=)
c.1572C>G (p.Ala524=)
c.1488C>G (p.Ala496=)
c.586C>G
c.1785C>G (p.Ala595=)
c.1374C>G (p.Ala458=)
n.1687C>G
5g.177095594C>TCA447725562FGFR4c.1692C>T (p.Ala564=)
c.1572C>T (p.Ala524=)
c.1488C>T (p.Ala496=)
c.586C>T
c.1785C>T (p.Ala595=)
c.1374C>T (p.Ala458=)
n.1687C>T
5g.177095595C>ACA447725563FGFR4c.1693C>A (p.Arg565=)
c.1573C>A (p.Arg525=)
c.1489C>A (p.Arg497=)
c.587C>A
c.1786C>A (p.Arg596=)
c.1375C>A (p.Arg459=)
n.1688C>A
 gnomAD v4
5g.177095595C=CA1603404322FGFR4c.1693C= (p.Arg565=)
c.1573C= (p.Arg525=)
c.1489C= (p.Arg497=)
c.587C=
c.1786C= (p.Arg596=)
c.1375C= (p.Arg459=)
n.1688C=
5g.177095595C>GCA362297173FGFR4c.1693C>G (p.Arg565Gly)
c.1573C>G (p.Arg525Gly)
c.1489C>G (p.Arg497Gly)
c.587C>G
c.1786C>G (p.Arg596Gly)
c.1375C>G (p.Arg459Gly)
n.1688C>G
5g.177095595C>TCA3576520FGFR4c.1693C>T (p.Arg565Trp)
c.1573C>T (p.Arg525Trp)
c.1489C>T (p.Arg497Trp)
c.587C>T
c.1786C>T (p.Arg596Trp)
c.1375C>T (p.Arg459Trp)
n.1688C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177095596G>ACA3576521FGFR4c.1694G>A (p.Arg565Gln)
c.1574G>A (p.Arg525Gln)
c.1490G>A (p.Arg497Gln)
c.588G>A
c.1787G>A (p.Arg596Gln)
c.1376G>A (p.Arg459Gln)
n.1689G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
5g.177095596G>CCA362297174FGFR4c.1694G>C (p.Arg565Pro)
c.1574G>C (p.Arg525Pro)
c.1490G>C (p.Arg497Pro)
c.588G>C
c.1787G>C (p.Arg596Pro)
c.1376G>C (p.Arg459Pro)
n.1689G>C
5g.177095596G=CA1603404323FGFR4c.1694G= (p.Arg565=)
c.1574G= (p.Arg525=)
c.1490G= (p.Arg497=)
c.588G=
c.1787G= (p.Arg596=)
c.1376G= (p.Arg459=)
n.1689G=
5g.177095596G>TCA362297175FGFR4c.1694G>T (p.Arg565Leu)
c.1574G>T (p.Arg525Leu)
c.1490G>T (p.Arg497Leu)
c.588G>T
c.1787G>T (p.Arg596Leu)
c.1376G>T (p.Arg459Leu)
n.1689G>T
5g.177095597G>ACA447725565FGFR4c.1695G>A (p.Arg565=)
c.1575G>A (p.Arg525=)
c.1491G>A (p.Arg497=)
c.589G>A
c.1788G>A (p.Arg596=)
c.1377G>A (p.Arg459=)
n.1690G>A
 gnomAD v4
5g.177095597G>CCA447725564FGFR4c.1695G>C (p.Arg565=)
c.1575G>C (p.Arg525=)
c.1491G>C (p.Arg497=)
c.589G>C
c.1788G>C (p.Arg596=)
c.1377G>C (p.Arg459=)
n.1690G>C
5g.177095597G>TCA447725566FGFR4c.1695G>T (p.Arg565=)
c.1575G>T (p.Arg525=)
c.1491G>T (p.Arg497=)
c.589G>T
c.1788G>T (p.Arg596=)
c.1377G>T (p.Arg459=)
n.1690G>T
 gnomAD v4
5g.177095598C>ACA362297176FGFR4c.1696C>A (p.Arg566Ser)
c.1576C>A (p.Arg526Ser)
c.1492C>A (p.Arg498Ser)
c.590C>A
c.1789C>A (p.Arg597Ser)
c.1378C>A (p.Arg460Ser)
n.1691C>A
 gnomAD v4
5g.177095598C=CA1603404324FGFR4c.1696C= (p.Arg566=)
c.1576C= (p.Arg526=)
c.1492C= (p.Arg498=)
c.590C=
c.1789C= (p.Arg597=)
c.1378C= (p.Arg460=)
n.1691C=
5g.177095598C>GCA362297177FGFR4c.1696C>G (p.Arg566Gly)
c.1576C>G (p.Arg526Gly)
c.1492C>G (p.Arg498Gly)
c.590C>G
c.1789C>G (p.Arg597Gly)
c.1378C>G (p.Arg460Gly)
n.1691C>G
5g.177095598C>TCA3576522FGFR4c.1696C>T (p.Arg566Cys)
c.1576C>T (p.Arg526Cys)
c.1492C>T (p.Arg498Cys)
c.590C>T
c.1789C>T (p.Arg597Cys)
c.1378C>T (p.Arg460Cys)
n.1691C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
5g.177095599G>ACA362297178FGFR4c.1697G>A (p.Arg566His)
c.1577G>A (p.Arg526His)
c.1493G>A (p.Arg498His)
c.591G>A
c.1790G>A (p.Arg597His)
c.1379G>A (p.Arg460His)
n.1692G>A
 dbSNP gnomAD v4
5g.177095599G>CCA362297180FGFR4c.1697G>C (p.Arg566Pro)
c.1577G>C (p.Arg526Pro)
c.1493G>C (p.Arg498Pro)
c.591G>C
c.1790G>C (p.Arg597Pro)
c.1379G>C (p.Arg460Pro)
n.1692G>C
5g.177095599G=CA1603404325FGFR4c.1697G= (p.Arg566=)
c.1577G= (p.Arg526=)
c.1493G= (p.Arg498=)
c.591G=
c.1790G= (p.Arg597=)
c.1379G= (p.Arg460=)
n.1692G=
5g.177095599G>TCA362297179FGFR4c.1697G>T (p.Arg566Leu)
c.1577G>T (p.Arg526Leu)
c.1493G>T (p.Arg498Leu)
c.591G>T
c.1790G>T (p.Arg597Leu)
c.1379G>T (p.Arg460Leu)
n.1692G>T
 gnomAD v4
5g.177095600C>ACA132833159FGFR4c.1698C>A (p.Arg566=)
c.1578C>A (p.Arg526=)
c.1494C>A (p.Arg498=)
c.592C>A
c.1791C>A (p.Arg597=)
c.1380C>A (p.Arg460=)
n.1693C>A
 dbSNP gnomAD v4
5g.177095600C=CA1603404326FGFR4c.1698C= (p.Arg566=)
c.1578C= (p.Arg526=)
c.1494C= (p.Arg498=)
c.592C=
c.1791C= (p.Arg597=)
c.1380C= (p.Arg460=)
n.1693C=
5g.177095600C>GCA447725587FGFR4c.1698C>G (p.Arg566=)
c.1578C>G (p.Arg526=)
c.1494C>G (p.Arg498=)
c.592C>G
c.1791C>G (p.Arg597=)
c.1380C>G (p.Arg460=)
n.1693C>G
5g.177095600C>TCA447725588FGFR4c.1698C>T (p.Arg566=)
c.1578C>T (p.Arg526=)
c.1494C>T (p.Arg498=)
c.592C>T
c.1791C>T (p.Arg597=)
c.1380C>T (p.Arg460=)
n.1693C>T
 gnomAD v4
5g.177095605dupCA564898787FGFR4c.1703dup (p.Gly569ArgfsTer13)
c.1583dup (p.Gly529ArgfsTer13)
c.1499dup (p.Gly501ArgfsTer13)
c.597dup
c.1796dup (p.Gly600ArgfsTer13)
c.1385dup (p.Gly463ArgfsTer13)
n.1698dup
 dbSNP gnomAD v2 gnomAD v4
5g.177095605delCA645545683FGFR4c.1703del (p.Pro568GlnfsTer?)
c.1583del (p.Pro528GlnfsTer?)
c.1499del (p.Pro500GlnfsTer?)
c.597del
c.1796del (p.Pro599GlnfsTer?)
c.1385del (p.Pro462GlnfsTer?)
n.1698del
 gnomAD v4 COSMIC COSMIC
5g.177095601C>ACA362297181FGFR4c.1699C>A (p.Pro567Thr)
c.1579C>A (p.Pro527Thr)
c.1495C>A (p.Pro499Thr)
c.593C>A
c.1792C>A (p.Pro598Thr)
c.1381C>A (p.Pro461Thr)
n.1694C>A
 gnomAD v4
5g.177095601C=CA1603404327FGFR4c.1699C= (p.Pro567=)
c.1579C= (p.Pro527=)
c.1495C= (p.Pro499=)
c.593C=
c.1792C= (p.Pro598=)
c.1381C= (p.Pro461=)
n.1694C=
5g.177095601C>GCA362297182FGFR4c.1699C>G (p.Pro567Ala)
c.1579C>G (p.Pro527Ala)
c.1495C>G (p.Pro499Ala)
c.593C>G
c.1792C>G (p.Pro598Ala)
c.1381C>G (p.Pro461Ala)
n.1694C>G
5g.177095601C>TCA3576523FGFR4c.1699C>T (p.Pro567Ser)
c.1579C>T (p.Pro527Ser)
c.1495C>T (p.Pro499Ser)
c.593C>T
c.1792C>T (p.Pro598Ser)
c.1381C>T (p.Pro461Ser)
n.1694C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177095602C>ACA362297183FGFR4c.1700C>A (p.Pro567His)
c.1580C>A (p.Pro527His)
c.1496C>A (p.Pro499His)
c.594C>A
c.1793C>A (p.Pro598His)
c.1382C>A (p.Pro461His)
n.1695C>A
 dbSNP
5g.177095602C>GCA362297184FGFR4c.1700C>G (p.Pro567Arg)
c.1580C>G (p.Pro527Arg)
c.1496C>G (p.Pro499Arg)
c.594C>G
c.1793C>G (p.Pro598Arg)
c.1382C>G (p.Pro461Arg)
n.1695C>G
5g.177095602C>TCA362297185FGFR4c.1700C>T (p.Pro567Leu)
c.1580C>T (p.Pro527Leu)
c.1496C>T (p.Pro499Leu)
c.594C>T
c.1793C>T (p.Pro598Leu)
c.1382C>T (p.Pro461Leu)
n.1695C>T
5g.177095603C>ACA447725589FGFR4c.1701C>A (p.Pro567=)
c.1581C>A (p.Pro527=)
c.1497C>A (p.Pro499=)
c.595C>A
c.1794C>A (p.Pro598=)
c.1383C>A (p.Pro461=)
n.1696C>A
5g.177095603C=CA1603404328FGFR4c.1701C= (p.Pro567=)
c.1581C= (p.Pro527=)
c.1497C= (p.Pro499=)
c.595C=
c.1794C= (p.Pro598=)
c.1383C= (p.Pro461=)
n.1696C=
5g.177095603C>GCA447725590FGFR4c.1701C>G (p.Pro567=)
c.1581C>G (p.Pro527=)
c.1497C>G (p.Pro499=)
c.595C>G
c.1794C>G (p.Pro598=)
c.1383C>G (p.Pro461=)
n.1696C>G
 dbSNP gnomAD v3 gnomAD v4
5g.177095603C>TCA447725591FGFR4c.1701C>T (p.Pro567=)
c.1581C>T (p.Pro527=)
c.1497C>T (p.Pro499=)
c.595C>T
c.1794C>T (p.Pro598=)
c.1383C>T (p.Pro461=)
n.1696C>T
5g.177095604C>ACA362297186FGFR4c.1702C>A (p.Pro568Thr)
c.1582C>A (p.Pro528Thr)
c.1498C>A (p.Pro500Thr)
c.596C>A
c.1795C>A (p.Pro599Thr)
c.1384C>A (p.Pro462Thr)
n.1697C>A
 gnomAD v4
5g.177095604C=CA1603404329FGFR4c.1702C= (p.Pro568=)
c.1582C= (p.Pro528=)
c.1498C= (p.Pro500=)
c.596C=
c.1795C= (p.Pro599=)
c.1384C= (p.Pro462=)
n.1697C=
5g.177095604C>GCA3576524FGFR4c.1702C>G (p.Pro568Ala)
c.1582C>G (p.Pro528Ala)
c.1498C>G (p.Pro500Ala)
c.596C>G
c.1795C>G (p.Pro599Ala)
c.1384C>G (p.Pro462Ala)
n.1697C>G
 dbSNP ExAC gnomAD v2 gnomAD v4
5g.177095604C>TCA362297187FGFR4c.1702C>T (p.Pro568Ser)
c.1582C>T (p.Pro528Ser)
c.1498C>T (p.Pro500Ser)
c.596C>T
c.1795C>T (p.Pro599Ser)
c.1384C>T (p.Pro462Ser)
n.1697C>T
 gnomAD v4 COSMIC COSMIC
5g.177095605C>ACA3576525FGFR4c.1703C>A (p.Pro568Gln)
c.1583C>A (p.Pro528Gln)
c.1499C>A (p.Pro500Gln)
c.597C>A
c.1796C>A (p.Pro599Gln)
c.1385C>A (p.Pro462Gln)
n.1698C>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
5g.177095605C=CA1603404330FGFR4c.1703C= (p.Pro568=)
c.1583C= (p.Pro528=)
c.1499C= (p.Pro500=)
c.597C=
c.1796C= (p.Pro599=)
c.1385C= (p.Pro462=)
n.1698C=
5g.177095605C>GCA362297188FGFR4c.1703C>G (p.Pro568Arg)
c.1583C>G (p.Pro528Arg)
c.1499C>G (p.Pro500Arg)
c.597C>G
c.1796C>G (p.Pro599Arg)
c.1385C>G (p.Pro462Arg)
n.1698C>G
5g.177095605C>TCA362297189FGFR4c.1703C>T (p.Pro568Leu)
c.1583C>T (p.Pro528Leu)
c.1499C>T (p.Pro500Leu)
c.597C>T
c.1796C>T (p.Pro599Leu)
c.1385C>T (p.Pro462Leu)
n.1698C>T
5g.177095606A>CCA447725595FGFR4c.1704A>C (p.Pro568=)
c.1584A>C (p.Pro528=)
c.1500A>C (p.Pro500=)
c.598A>C
c.1797A>C (p.Pro599=)
c.1386A>C (p.Pro462=)
n.1699A>C
5g.177095606A>GCA447725596FGFR4c.1704A>G (p.Pro568=)
c.1584A>G (p.Pro528=)
c.1500A>G (p.Pro500=)
c.598A>G
c.1797A>G (p.Pro599=)
c.1386A>G (p.Pro462=)
n.1699A>G
 gnomAD v4
5g.177095606A>TCA447725597FGFR4c.1704A>T (p.Pro568=)
c.1584A>T (p.Pro528=)
c.1500A>T (p.Pro500=)
c.598A>T
c.1797A>T (p.Pro599=)
c.1386A>T (p.Pro462=)
n.1699A>T
5g.177095607G>ACA362297191FGFR4c.1705G>A (p.Gly569Ser)
c.1585G>A (p.Gly529Ser)
c.1501G>A (p.Gly501Ser)
c.599G>A
c.1798G>A (p.Gly600Ser)
c.1387G>A (p.Gly463Ser)
n.1700G>A
5g.177095607G>CCA362297192FGFR4c.1705G>C (p.Gly569Arg)
c.1585G>C (p.Gly529Arg)
c.1501G>C (p.Gly501Arg)
c.599G>C
c.1798G>C (p.Gly600Arg)
c.1387G>C (p.Gly463Arg)
n.1700G>C
 dbSNP
5g.177095607G=CA1603404331FGFR4c.1705G= (p.Gly569=)
c.1585G= (p.Gly529=)
c.1501G= (p.Gly501=)
c.599G=
c.1798G= (p.Gly600=)
c.1387G= (p.Gly463=)
n.1700G=
5g.177095607G>TCA362297190FGFR4c.1705G>T (p.Gly569Cys)
c.1585G>T (p.Gly529Cys)
c.1501G>T (p.Gly501Cys)
c.599G>T
c.1798G>T (p.Gly600Cys)
c.1387G>T (p.Gly463Cys)
n.1700G>T
 COSMIC COSMIC
5g.177095608G>ACA362297193FGFR4c.1706G>A (p.Gly569Asp)
c.1586G>A (p.Gly529Asp)
c.1502G>A (p.Gly501Asp)
c.600G>A
c.1799G>A (p.Gly600Asp)
c.1388G>A (p.Gly463Asp)
n.1701G>A
5g.177095608G>CCA362297195FGFR4c.1706G>C (p.Gly569Ala)
c.1586G>C (p.Gly529Ala)
c.1502G>C (p.Gly501Ala)
c.600G>C
c.1799G>C (p.Gly600Ala)
c.1388G>C (p.Gly463Ala)
n.1701G>C
5g.177095608G>TCA362297194FGFR4c.1706G>T (p.Gly569Val)
c.1586G>T (p.Gly529Val)
c.1502G>T (p.Gly501Val)
c.600G>T
c.1799G>T (p.Gly600Val)
c.1388G>T (p.Gly463Val)
n.1701G>T
5g.177095608_177095609delinsGCCA1603404333FGFR4c.1706_1707delinsGC (p.Gly569=)
c.1586_1587delinsGC (p.Gly529=)
c.1502_1503delinsGC (p.Gly501=)
c.600_601delinsGC
c.1799_1800delinsGC (p.Gly600=)
c.1388_1389delinsGC (p.Gly463=)
n.1701_1702delinsGC
5g.177095616_177095627dupCA1603404332FGFR4c.1714_1725dup (p.Asp575_Gly576insLeuSerProAsp)
c.1594_1605dup (p.Asp535_Gly536insLeuSerProAsp)
c.1510_1521dup (p.Asp507_Gly508insLeuSerProAsp)
c.608_619dup
c.1807_1818dup (p.Asp606_Gly607insLeuSerProAsp)
c.1396_1407dup (p.Asp469_Gly470insLeuSerProAsp)
n.1709_1720dup
 dbSNP gnomAD v4
5g.177095616_177095627delCA2676683397FGFR4c.1714_1725del (p.Leu572_Asp575del)
c.1594_1605del (p.Leu532_Asp535del)
c.1510_1521del (p.Leu504_Asp507del)
c.608_619del
c.1807_1818del (p.Leu603_Asp606del)
c.1396_1407del (p.Leu466_Asp469del)
n.1709_1720del
 gnomAD v4
5g.177095609C>ACA447725599FGFR4c.1707C>A (p.Gly569=)
c.1587C>A (p.Gly529=)
c.1503C>A (p.Gly501=)
c.601C>A
c.1800C>A (p.Gly600=)
c.1389C>A (p.Gly463=)
n.1702C>A
 gnomAD v4
5g.177095609C>GCA447725600FGFR4c.1707C>G (p.Gly569=)
c.1587C>G (p.Gly529=)
c.1503C>G (p.Gly501=)
c.601C>G
c.1800C>G (p.Gly600=)
c.1389C>G (p.Gly463=)
n.1702C>G
5g.177095609C>TCA447725601FGFR4c.1707C>T (p.Gly569=)
c.1587C>T (p.Gly529=)
c.1503C>T (p.Gly501=)
c.601C>T
c.1800C>T (p.Gly600=)
c.1389C>T (p.Gly463=)
n.1702C>T
5g.177095612delCA1603404334FGFR4c.1710del (p.Asp571ThrfsTer?)
c.1590del (p.Asp531ThrfsTer?)
c.1506del (p.Asp503ThrfsTer?)
c.604del
c.1803del (p.Asp602ThrfsTer?)
c.1392del (p.Asp465ThrfsTer?)
n.1705del
 dbSNP
5g.177095610C>ACA362297196FGFR4c.1708C>A (p.Pro570Thr)
c.1588C>A (p.Pro530Thr)
c.1504C>A (p.Pro502Thr)
c.602C>A
c.1801C>A (p.Pro601Thr)
c.1390C>A (p.Pro464Thr)
n.1703C>A
5g.177095610C>GCA362297198FGFR4c.1708C>G (p.Pro570Ala)
c.1588C>G (p.Pro530Ala)
c.1504C>G (p.Pro502Ala)
c.602C>G
c.1801C>G (p.Pro601Ala)
c.1390C>G (p.Pro464Ala)
n.1703C>G
5g.177095610C>TCA362297197FGFR4c.1708C>T (p.Pro570Ser)
c.1588C>T (p.Pro530Ser)
c.1504C>T (p.Pro502Ser)
c.602C>T
c.1801C>T (p.Pro601Ser)
c.1390C>T (p.Pro464Ser)
n.1703C>T
5g.177095611C>ACA362297199FGFR4c.1709C>A (p.Pro570His)
c.1589C>A (p.Pro530His)
c.1505C>A (p.Pro502His)
c.603C>A
c.1802C>A (p.Pro601His)
c.1391C>A (p.Pro464His)
n.1704C>A
5g.177095611C>GCA362297201FGFR4c.1709C>G (p.Pro570Arg)
c.1589C>G (p.Pro530Arg)
c.1505C>G (p.Pro502Arg)
c.603C>G
c.1802C>G (p.Pro601Arg)
c.1391C>G (p.Pro464Arg)
n.1704C>G
5g.177095611C>TCA362297200FGFR4c.1709C>T (p.Pro570Leu)
c.1589C>T (p.Pro530Leu)
c.1505C>T (p.Pro502Leu)
c.603C>T
c.1802C>T (p.Pro601Leu)
c.1391C>T (p.Pro464Leu)
n.1704C>T
 gnomAD v4
5g.177095612C>ACA3576528FGFR4c.1710C>A (p.Pro570=)
c.1590C>A (p.Pro530=)
c.1506C>A (p.Pro502=)
c.604C>A
c.1803C>A (p.Pro601=)
c.1392C>A (p.Pro464=)
n.1705C>A
 dbSNP ExAC gnomAD v2 gnomAD v4
5g.177095612C=CA1603404335FGFR4c.1710C= (p.Pro570=)
c.1590C= (p.Pro530=)
c.1506C= (p.Pro502=)
c.604C=
c.1803C= (p.Pro601=)
c.1392C= (p.Pro464=)
n.1705C=
5g.177095612C>GCA3576527FGFR4c.1710C>G (p.Pro570=)
c.1590C>G (p.Pro530=)
c.1506C>G (p.Pro502=)
c.604C>G
c.1803C>G (p.Pro601=)
c.1392C>G (p.Pro464=)
n.1705C>G
 dbSNP ExAC gnomAD v4
5g.177095612C>TCA3576526FGFR4c.1710C>T (p.Pro570=)
c.1590C>T (p.Pro530=)
c.1506C>T (p.Pro502=)
c.604C>T
c.1803C>T (p.Pro601=)
c.1392C>T (p.Pro464=)
n.1705C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177095613G>ACA3576529FGFR4c.1711G>A (p.Asp571Asn)
c.1591G>A (p.Asp531Asn)
c.1507G>A (p.Asp503Asn)
c.605G>A
c.1804G>A (p.Asp602Asn)
c.1393G>A (p.Asp465Asn)
n.1706G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
5g.177095613G>CCA362297203FGFR4c.1711G>C (p.Asp571His)
c.1591G>C (p.Asp531His)
c.1507G>C (p.Asp503His)
c.605G>C
c.1804G>C (p.Asp602His)
c.1393G>C (p.Asp465His)
n.1706G>C
 dbSNP gnomAD v4
5g.177095613G=CA1603404336FGFR4c.1711G= (p.Asp571=)
c.1591G= (p.Asp531=)
c.1507G= (p.Asp503=)
c.605G=
c.1804G= (p.Asp602=)
c.1393G= (p.Asp465=)
n.1706G=
5g.177095613G>TCA362297202FGFR4c.1711G>T (p.Asp571Tyr)
c.1591G>T (p.Asp531Tyr)
c.1507G>T (p.Asp503Tyr)
c.605G>T
c.1804G>T (p.Asp602Tyr)
c.1393G>T (p.Asp465Tyr)
n.1706G>T
 gnomAD v4
5g.177095614_177095620dupCA564898788FGFR4c.1712_1718dup (p.Ser573ArgfsTer11)
c.1592_1598dup (p.Ser533ArgfsTer11)
c.1508_1514dup (p.Ser505ArgfsTer11)
c.606_612dup
c.1805_1811dup (p.Ser604ArgfsTer11)
c.1394_1400dup (p.Ser467ArgfsTer11)
n.1707_1713dup
 dbSNP gnomAD v2 gnomAD v4
5g.177095614A=CA1603404337FGFR4c.1712A= (p.Asp571=)
c.1592A= (p.Asp531=)
c.1508A= (p.Asp503=)
c.606A=
c.1805A= (p.Asp602=)
c.1394A= (p.Asp465=)
n.1707A=
5g.177095614A>CCA362297204FGFR4c.1712A>C (p.Asp571Ala)
c.1592A>C (p.Asp531Ala)
c.1508A>C (p.Asp503Ala)
c.606A>C
c.1805A>C (p.Asp602Ala)
c.1394A>C (p.Asp465Ala)
n.1707A>C
 dbSNP
5g.177095614A>GCA362297205FGFR4c.1712A>G (p.Asp571Gly)
c.1592A>G (p.Asp531Gly)
c.1508A>G (p.Asp503Gly)
c.606A>G
c.1805A>G (p.Asp602Gly)
c.1394A>G (p.Asp465Gly)
n.1707A>G
5g.177095614A>TCA3576530FGFR4c.1712A>T (p.Asp571Val)
c.1592A>T (p.Asp531Val)
c.1508A>T (p.Asp503Val)
c.606A>T
c.1805A>T (p.Asp602Val)
c.1394A>T (p.Asp465Val)
n.1707A>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177095615C>ACA362297206FGFR4c.1713C>A (p.Asp571Glu)
c.1593C>A (p.Asp531Glu)
c.1509C>A (p.Asp503Glu)
c.607C>A
c.1806C>A (p.Asp602Glu)
c.1395C>A (p.Asp465Glu)
n.1708C>A
 dbSNP
5g.177095615C=CA1603404338FGFR4c.1713C= (p.Asp571=)
c.1593C= (p.Asp531=)
c.1509C= (p.Asp503=)
c.607C=
c.1806C= (p.Asp602=)
c.1395C= (p.Asp465=)
n.1708C=
5g.177095615C>GCA362297207FGFR4c.1713C>G (p.Asp571Glu)
c.1593C>G (p.Asp531Glu)
c.1509C>G (p.Asp503Glu)
c.607C>G
c.1806C>G (p.Asp602Glu)
c.1395C>G (p.Asp465Glu)
n.1708C>G
 dbSNP gnomAD v2 gnomAD v4
5g.177095615C>TCA3576531FGFR4c.1713C>T (p.Asp571=)
c.1593C>T (p.Asp531=)
c.1509C>T (p.Asp503=)
c.607C>T
c.1806C>T (p.Asp602=)
c.1395C>T (p.Asp465=)
n.1708C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
5g.177095616C>ACA362297208FGFR4c.1714C>A (p.Leu572Ile)
c.1594C>A (p.Leu532Ile)
c.1510C>A (p.Leu504Ile)
c.608C>A
c.1807C>A (p.Leu603Ile)
c.1396C>A (p.Leu466Ile)
n.1709C>A
 dbSNP
5g.177095616C>GCA362297209FGFR4c.1714C>G (p.Leu572Val)
c.1594C>G (p.Leu532Val)
c.1510C>G (p.Leu504Val)
c.608C>G
c.1807C>G (p.Leu603Val)
c.1396C>G (p.Leu466Val)
n.1709C>G
 gnomAD v4
5g.177095616C>TCA362297210FGFR4c.1714C>T (p.Leu572Phe)
c.1594C>T (p.Leu532Phe)
c.1510C>T (p.Leu504Phe)
c.608C>T
c.1807C>T (p.Leu603Phe)
c.1396C>T (p.Leu466Phe)
n.1709C>T
5g.177095616_177095628delinsCTCAGCCCCGACGCA1603404339FGFR4c.1714_1726delinsCTCAGCCCCGACG (p.Leu572=)
c.1594_1606delinsCTCAGCCCCGACG (p.Leu532=)
c.1510_1522delinsCTCAGCCCCGACG (p.Leu504=)
c.608_620delinsCTCAGCCCCGACG
c.1807_1819delinsCTCAGCCCCGACG (p.Leu603=)
c.1396_1408delinsCTCAGCCCCGACG (p.Leu466=)
n.1709_1721delinsCTCAGCCCCGACG
5g.177095617T>ACA362297211FGFR4c.1715T>A (p.Leu572His)
c.1595T>A (p.Leu532His)
c.1511T>A (p.Leu504His)
c.609T>A
c.1808T>A (p.Leu603His)
c.1397T>A (p.Leu466His)
n.1710T>A
5g.177095617T>CCA362297212FGFR4c.1715T>C (p.Leu572Pro)
c.1595T>C (p.Leu532Pro)
c.1511T>C (p.Leu504Pro)
c.609T>C
c.1808T>C (p.Leu603Pro)
c.1397T>C (p.Leu466Pro)
n.1710T>C
5g.177095617T>GCA362297213FGFR4c.1715T>G (p.Leu572Arg)
c.1595T>G (p.Leu532Arg)
c.1511T>G (p.Leu504Arg)
c.609T>G
c.1808T>G (p.Leu603Arg)
c.1397T>G (p.Leu466Arg)
n.1710T>G
5g.177095617_177095628delCA132833198FGFR4c.1715_1726del (p.Leu572_Gly576delinsArg)
c.1595_1606del (p.Leu532_Gly536delinsArg)
c.1511_1522del (p.Leu504_Gly508delinsArg)
c.609_620del
c.1808_1819del (p.Leu603_Gly607delinsArg)
c.1397_1408del (p.Leu466_Gly470delinsArg)
n.1710_1721del
 dbSNP gnomAD v2 gnomAD v4
5g.177095618C>ACA447725611FGFR4c.1716C>A (p.Leu572=)
c.1596C>A (p.Leu532=)
c.1512C>A (p.Leu504=)
c.610C>A
c.1809C>A (p.Leu603=)
c.1398C>A (p.Leu466=)
n.1711C>A
5g.177095618C=CA1603404340FGFR4c.1716C= (p.Leu572=)
c.1596C= (p.Leu532=)
c.1512C= (p.Leu504=)
c.610C=
c.1809C= (p.Leu603=)
c.1398C= (p.Leu466=)
n.1711C=
5g.177095618C>GCA447725612FGFR4c.1716C>G (p.Leu572=)
c.1596C>G (p.Leu532=)
c.1512C>G (p.Leu504=)
c.610C>G
c.1809C>G (p.Leu603=)
c.1398C>G (p.Leu466=)
n.1711C>G
5g.177095618C>TCA447725610FGFR4c.1716C>T (p.Leu572=)
c.1596C>T (p.Leu532=)
c.1512C>T (p.Leu504=)
c.610C>T
c.1809C>T (p.Leu603=)
c.1398C>T (p.Leu466=)
n.1711C>T
 dbSNP gnomAD v2 gnomAD v4
5g.177095619A>CCA362297214FGFR4c.1717A>C (p.Ser573Arg)
c.1597A>C (p.Ser533Arg)
c.1513A>C (p.Ser505Arg)
c.611A>C
c.1810A>C (p.Ser604Arg)
c.1399A>C (p.Ser467Arg)
n.1712A>C
5g.177095619A>GCA362297215FGFR4c.1717A>G (p.Ser573Gly)
c.1597A>G (p.Ser533Gly)
c.1513A>G (p.Ser505Gly)
c.611A>G
c.1810A>G (p.Ser604Gly)
c.1399A>G (p.Ser467Gly)
n.1712A>G
5g.177095619A>TCA362297216FGFR4c.1717A>T (p.Ser573Cys)
c.1597A>T (p.Ser533Cys)
c.1513A>T (p.Ser505Cys)
c.611A>T
c.1810A>T (p.Ser604Cys)
c.1399A>T (p.Ser467Cys)
n.1712A>T
5g.177095620G>ACA362297217FGFR4c.1718G>A (p.Ser573Asn)
c.1598G>A (p.Ser533Asn)
c.1514G>A (p.Ser505Asn)
c.612G>A
c.1811G>A (p.Ser604Asn)
c.1400G>A (p.Ser467Asn)
n.1713G>A
 dbSNP gnomAD v2 gnomAD v4
5g.177095620G>CCA362297218FGFR4c.1718G>C (p.Ser573Thr)
c.1598G>C (p.Ser533Thr)
c.1514G>C (p.Ser505Thr)
c.612G>C
c.1811G>C (p.Ser604Thr)
c.1400G>C (p.Ser467Thr)
n.1713G>C
 dbSNP
5g.177095620G=CA1603404341FGFR4c.1718G= (p.Ser573=)
c.1598G= (p.Ser533=)
c.1514G= (p.Ser505=)
c.612G=
c.1811G= (p.Ser604=)
c.1400G= (p.Ser467=)
n.1713G=
5g.177095620G>TCA3576533FGFR4c.1718G>T (p.Ser573Ile)
c.1598G>T (p.Ser533Ile)
c.1514G>T (p.Ser505Ile)
c.612G>T
c.1811G>T (p.Ser604Ile)
c.1400G>T (p.Ser467Ile)
n.1713G>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177095620_177095621delinsGCCA1603404342FGFR4c.1718_1719delinsGC (p.Ser573=)
c.1598_1599delinsGC (p.Ser533=)
c.1514_1515delinsGC (p.Ser505=)
c.612_613delinsGC
c.1811_1812delinsGC (p.Ser604=)
c.1400_1401delinsGC (p.Ser467=)
n.1713_1714delinsGC
5g.177095621C>ACA362297219FGFR4c.1719C>A (p.Ser573Arg)
c.1599C>A (p.Ser533Arg)
c.1515C>A (p.Ser505Arg)
c.613C>A
c.1812C>A (p.Ser604Arg)
c.1401C>A (p.Ser467Arg)
n.1714C>A
 dbSNP
5g.177095621C>GCA362297220FGFR4c.1719C>G (p.Ser573Arg)
c.1599C>G (p.Ser533Arg)
c.1515C>G (p.Ser505Arg)
c.613C>G
c.1812C>G (p.Ser604Arg)
c.1401C>G (p.Ser467Arg)
n.1714C>G
5g.177095621C>TCA447725613FGFR4c.1719C>T (p.Ser573=)
c.1599C>T (p.Ser533=)
c.1515C>T (p.Ser505=)
c.613C>T
c.1812C>T (p.Ser604=)
c.1401C>T (p.Ser467=)
n.1714C>T
 dbSNP gnomAD v4
5g.177095624delCA3576532FGFR4c.1722del (p.Asp575ThrfsTer?)
c.1602del (p.Asp535ThrfsTer?)
c.1518del (p.Asp507ThrfsTer?)
c.616del
c.1815del (p.Asp606ThrfsTer?)
c.1404del (p.Asp469ThrfsTer?)
n.1717del
 dbSNP ExAC gnomAD v2 gnomAD v4
5g.177095622C>ACA362297221FGFR4c.1720C>A (p.Pro574Thr)
c.1600C>A (p.Pro534Thr)
c.1516C>A (p.Pro506Thr)
c.614C>A
c.1813C>A (p.Pro605Thr)
c.1402C>A (p.Pro468Thr)
n.1715C>A
 gnomAD v4
5g.177095622C=CA1603404343FGFR4c.1720C= (p.Pro574=)
c.1600C= (p.Pro534=)
c.1516C= (p.Pro506=)
c.614C=
c.1813C= (p.Pro605=)
c.1402C= (p.Pro468=)
n.1715C=
5g.177095622C>GCA362297222FGFR4c.1720C>G (p.Pro574Ala)
c.1600C>G (p.Pro534Ala)
c.1516C>G (p.Pro506Ala)
c.614C>G
c.1813C>G (p.Pro605Ala)
c.1402C>G (p.Pro468Ala)
n.1715C>G
5g.177095622C>TCA3576534FGFR4c.1720C>T (p.Pro574Ser)
c.1600C>T (p.Pro534Ser)
c.1516C>T (p.Pro506Ser)
c.614C>T
c.1813C>T (p.Pro605Ser)
c.1402C>T (p.Pro468Ser)
n.1715C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
5g.177095623C>ACA362297223FGFR4c.1721C>A (p.Pro574His)
c.1601C>A (p.Pro534His)
c.1517C>A (p.Pro506His)
c.615C>A
c.1814C>A (p.Pro605His)
c.1403C>A (p.Pro468His)
n.1716C>A
5g.177095623C>GCA362297224FGFR4c.1721C>G (p.Pro574Arg)
c.1601C>G (p.Pro534Arg)
c.1517C>G (p.Pro506Arg)
c.615C>G
c.1814C>G (p.Pro605Arg)
c.1403C>G (p.Pro468Arg)
n.1716C>G
5g.177095623C>TCA362297225FGFR4c.1721C>T (p.Pro574Leu)
c.1601C>T (p.Pro534Leu)
c.1517C>T (p.Pro506Leu)
c.615C>T
c.1814C>T (p.Pro605Leu)
c.1403C>T (p.Pro468Leu)
n.1716C>T
5g.177095624C>ACA447725617FGFR4c.1722C>A (p.Pro574=)
c.1602C>A (p.Pro534=)
c.1518C>A (p.Pro506=)
c.616C>A
c.1815C>A (p.Pro605=)
c.1404C>A (p.Pro468=)
n.1717C>A
 dbSNP gnomAD v2 gnomAD v4
5g.177095624C=CA1603404344FGFR4c.1722C= (p.Pro574=)
c.1602C= (p.Pro534=)
c.1518C= (p.Pro506=)
c.616C=
c.1815C= (p.Pro605=)
c.1404C= (p.Pro468=)
n.1717C=
5g.177095624C>GCA447725618FGFR4c.1722C>G (p.Pro574=)
c.1602C>G (p.Pro534=)
c.1518C>G (p.Pro506=)
c.616C>G
c.1815C>G (p.Pro605=)
c.1404C>G (p.Pro468=)
n.1717C>G
 dbSNP gnomAD v4
5g.177095624C>TCA3576535FGFR4c.1722C>T (p.Pro574=)
c.1602C>T (p.Pro534=)
c.1518C>T (p.Pro506=)
c.616C>T
c.1815C>T (p.Pro605=)
c.1404C>T (p.Pro468=)
n.1717C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177095625G>ACA3576536FGFR4c.1723G>A (p.Asp575Asn)
c.1603G>A (p.Asp535Asn)
c.1519G>A (p.Asp507Asn)
c.617G>A
c.1816G>A (p.Asp606Asn)
c.1405G>A (p.Asp469Asn)
n.1718G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177095625G>CCA362297226FGFR4c.1723G>C (p.Asp575His)
c.1603G>C (p.Asp535His)
c.1519G>C (p.Asp507His)
c.617G>C
c.1816G>C (p.Asp606His)
c.1405G>C (p.Asp469His)
n.1718G>C
 dbSNP gnomAD v4
5g.177095625G=CA1603404345FGFR4c.1723G= (p.Asp575=)
c.1603G= (p.Asp535=)
c.1519G= (p.Asp507=)
c.617G=
c.1816G= (p.Asp606=)
c.1405G= (p.Asp469=)
n.1718G=
5g.177095625G>TCA362297227FGFR4c.1723G>T (p.Asp575Tyr)
c.1603G>T (p.Asp535Tyr)
c.1519G>T (p.Asp507Tyr)
c.617G>T
c.1816G>T (p.Asp606Tyr)
c.1405G>T (p.Asp469Tyr)
n.1718G>T
 gnomAD v4
5g.177095626_177095629dupCA2676683413FGFR4c.1724_1727dup (p.Pro577ArgfsTer6)
c.1604_1607dup (p.Pro537ArgfsTer6)
c.1520_1523dup (p.Pro509ArgfsTer6)
c.618_621dup
c.1817_1820dup (p.Pro608ArgfsTer6)
c.1406_1409dup (p.Pro471ArgfsTer6)
n.1719_1722dup
 gnomAD v4
5g.177095626A=CA1603404346FGFR4c.1724A= (p.Asp575=)
c.1604A= (p.Asp535=)
c.1520A= (p.Asp507=)
c.618A=
c.1817A= (p.Asp606=)
c.1406A= (p.Asp469=)
n.1719A=
5g.177095626A>CCA362297228FGFR4c.1724A>C (p.Asp575Ala)
c.1604A>C (p.Asp535Ala)
c.1520A>C (p.Asp507Ala)
c.618A>C
c.1817A>C (p.Asp606Ala)
c.1406A>C (p.Asp469Ala)
n.1719A>C
 dbSNP
5g.177095626A>GCA362297229FGFR4c.1724A>G (p.Asp575Gly)
c.1604A>G (p.Asp535Gly)
c.1520A>G (p.Asp507Gly)
c.618A>G
c.1817A>G (p.Asp606Gly)
c.1406A>G (p.Asp469Gly)
n.1719A>G
 dbSNP
5g.177095626A>TCA3576537FGFR4c.1724A>T (p.Asp575Val)
c.1604A>T (p.Asp535Val)
c.1520A>T (p.Asp507Val)
c.618A>T
c.1817A>T (p.Asp606Val)
c.1406A>T (p.Asp469Val)
n.1719A>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
5g.177095627C>ACA362297230FGFR4c.1725C>A (p.Asp575Glu)
c.1605C>A (p.Asp535Glu)
c.1521C>A (p.Asp507Glu)
c.619C>A
c.1818C>A (p.Asp606Glu)
c.1407C>A (p.Asp469Glu)
n.1720C>A
5g.177095627C=CA1603404347FGFR4c.1725C= (p.Asp575=)
c.1605C= (p.Asp535=)
c.1521C= (p.Asp507=)
c.619C=
c.1818C= (p.Asp606=)
c.1407C= (p.Asp469=)
n.1720C=
5g.177095627C>GCA132833253FGFR4c.1725C>G (p.Asp575Glu)
c.1605C>G (p.Asp535Glu)
c.1521C>G (p.Asp507Glu)
c.619C>G
c.1818C>G (p.Asp606Glu)
c.1407C>G (p.Asp469Glu)
n.1720C>G
 dbSNP gnomAD v4
5g.177095627C>TCA3576538FGFR4c.1725C>T (p.Asp575=)
c.1605C>T (p.Asp535=)
c.1521C>T (p.Asp507=)
c.619C>T
c.1818C>T (p.Asp606=)
c.1407C>T (p.Asp469=)
n.1720C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
5g.177095628_177095632dupCA2606563285FGFR4c.1726_1730dup (p.Arg578ValfsTer?)
c.1606_1610dup (p.Arg538ValfsTer?)
c.1522_1526dup (p.Arg510ValfsTer?)
c.620_624dup
c.1819_1823dup (p.Arg609ValfsTer?)
c.1408_1412dup (p.Arg472ValfsTer?)
n.1721_1725dup
 dbSNP gnomAD v3
5g.177095630_177095636dupCA132833243FGFR4c.1728_1734dup (p.Gly582GlnfsTer2)
c.1608_1614dup (p.Gly542GlnfsTer2)
c.1524_1530dup (p.Gly514GlnfsTer2)
c.622_628dup
c.1821_1827dup (p.Gly613GlnfsTer2)
c.1410_1416dup (p.Gly476GlnfsTer2)
n.1723_1729dup
 dbSNP gnomAD v4
5g.177095630_177095636delCA2578494400FGFR4c.1728_1734del (p.Pro577AlafsTer?)
c.1608_1614del (p.Pro537AlafsTer?)
c.1524_1530del (p.Pro509AlafsTer?)
c.622_628del
c.1821_1827del (p.Pro608AlafsTer?)
c.1410_1416del (p.Pro471AlafsTer?)
n.1723_1729del
5g.177095628G>ACA3576539FGFR4c.1726G>A (p.Gly576Ser)
c.1606G>A (p.Gly536Ser)
c.1522G>A (p.Gly508Ser)
c.620G>A
c.1819G>A (p.Gly607Ser)
c.1408G>A (p.Gly470Ser)
n.1721G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177095628G>CCA362297231FGFR4c.1726G>C (p.Gly576Arg)
c.1606G>C (p.Gly536Arg)
c.1522G>C (p.Gly508Arg)
c.620G>C
c.1819G>C (p.Gly607Arg)
c.1408G>C (p.Gly470Arg)
n.1721G>C
 dbSNP
5g.177095628G=CA1603404348FGFR4c.1726G= (p.Gly576=)
c.1606G= (p.Gly536=)
c.1522G= (p.Gly508=)
c.620G=
c.1819G= (p.Gly607=)
c.1408G= (p.Gly470=)
n.1721G=
5g.177095628G>TCA362297232FGFR4c.1726G>T (p.Gly576Cys)
c.1606G>T (p.Gly536Cys)
c.1522G>T (p.Gly508Cys)
c.620G>T
c.1819G>T (p.Gly607Cys)
c.1408G>T (p.Gly470Cys)
n.1721G>T
 gnomAD v4
5g.177095629G>ACA3576540FGFR4c.1727G>A (p.Gly576Asp)
c.1607G>A (p.Gly536Asp)
c.1523G>A (p.Gly508Asp)
c.621G>A
c.1820G>A (p.Gly607Asp)
c.1409G>A (p.Gly470Asp)
n.1722G>A
 dbSNP ExAC gnomAD v2 gnomAD v4
5g.177095629G>CCA362297233FGFR4c.1727G>C (p.Gly576Ala)
c.1607G>C (p.Gly536Ala)
c.1523G>C (p.Gly508Ala)
c.621G>C
c.1820G>C (p.Gly607Ala)
c.1409G>C (p.Gly470Ala)
n.1722G>C
 dbSNP
5g.177095629G=CA1603404349FGFR4c.1727G= (p.Gly576=)
c.1607G= (p.Gly536=)
c.1523G= (p.Gly508=)
c.621G=
c.1820G= (p.Gly607=)
c.1409G= (p.Gly470=)
n.1722G=
5g.177095629G>TCA362297234FGFR4c.1727G>T (p.Gly576Val)
c.1607G>T (p.Gly536Val)
c.1523G>T (p.Gly508Val)
c.621G>T
c.1820G>T (p.Gly607Val)
c.1409G>T (p.Gly470Val)
n.1722G>T
5g.177095630T>ACA447725623FGFR4c.1728T>A (p.Gly576=)
c.1608T>A (p.Gly536=)
c.1524T>A (p.Gly508=)
c.622T>A
c.1821T>A (p.Gly607=)
c.1410T>A (p.Gly470=)
n.1723T>A
 dbSNP
5g.177095630T>CCA447725624FGFR4c.1728T>C (p.Gly576=)
c.1608T>C (p.Gly536=)
c.1524T>C (p.Gly508=)
c.622T>C
c.1821T>C (p.Gly607=)
c.1410T>C (p.Gly470=)
n.1723T>C
5g.177095630T>GCA447725625FGFR4c.1728T>G (p.Gly576=)
c.1608T>G (p.Gly536=)
c.1524T>G (p.Gly508=)
c.622T>G
c.1821T>G (p.Gly607=)
c.1410T>G (p.Gly470=)
n.1723T>G
 dbSNP
5g.177095632_177095654delCA2676683414FGFR4c.1730_1752del (p.Pro577LeufsTer?)
c.1610_1632del (p.Pro537LeufsTer?)
c.1526_1548del (p.Pro509LeufsTer?)
c.624_646del
c.1823_1845del (p.Pro608LeufsTer?)
c.1412_1434del (p.Pro471LeufsTer?)
n.1725_1747del
 gnomAD v4
5g.177095631C>ACA362297235FGFR4c.1729C>A (p.Pro577Thr)
c.1609C>A (p.Pro537Thr)
c.1525C>A (p.Pro509Thr)
c.623C>A
c.1822C>A (p.Pro608Thr)
c.1411C>A (p.Pro471Thr)
n.1724C>A
 dbSNP gnomAD v4
5g.177095631C>GCA362297236FGFR4c.1729C>G (p.Pro577Ala)
c.1609C>G (p.Pro537Ala)
c.1525C>G (p.Pro509Ala)
c.623C>G
c.1822C>G (p.Pro608Ala)
c.1411C>G (p.Pro471Ala)
n.1724C>G
 gnomAD v4
5g.177095631C>TCA362297237FGFR4c.1729C>T (p.Pro577Ser)
c.1609C>T (p.Pro537Ser)
c.1525C>T (p.Pro509Ser)
c.623C>T
c.1822C>T (p.Pro608Ser)
c.1411C>T (p.Pro471Ser)
n.1724C>T
5g.177095632C>ACA362297238FGFR4c.1730C>A (p.Pro577His)
c.1610C>A (p.Pro537His)
c.1526C>A (p.Pro509His)
c.624C>A
c.1823C>A (p.Pro608His)
c.1412C>A (p.Pro471His)
n.1725C>A
 gnomAD v4
5g.177095632C>GCA362297239FGFR4c.1730C>G (p.Pro577Arg)
c.1610C>G (p.Pro537Arg)
c.1526C>G (p.Pro509Arg)
c.624C>G
c.1823C>G (p.Pro608Arg)
c.1412C>G (p.Pro471Arg)
n.1725C>G
5g.177095632C>TCA362297240FGFR4c.1730C>T (p.Pro577Leu)
c.1610C>T (p.Pro537Leu)
c.1526C>T (p.Pro509Leu)
c.624C>T
c.1823C>T (p.Pro608Leu)
c.1412C>T (p.Pro471Leu)
n.1725C>T
 gnomAD v4
5g.177095632_177095633insAGCA2676683415FGFR4c.1730_1731insAG (p.Arg578ValfsTer?)
c.1610_1611insAG (p.Arg538ValfsTer?)
c.1526_1527insAG (p.Arg510ValfsTer?)
c.624_625insAG
c.1823_1824insAG (p.Arg609ValfsTer?)
c.1412_1413insAG (p.Arg472ValfsTer?)
n.1725_1726insAG
 gnomAD v4
5g.177095633T>ACA447725629FGFR4c.1731T>A (p.Pro577=)
c.1611T>A (p.Pro537=)
c.1527T>A (p.Pro509=)
c.625T>A
c.1824T>A (p.Pro608=)
c.1413T>A (p.Pro471=)
n.1726T>A
 dbSNP
5g.177095633T>CCA447725626FGFR4c.1731T>C (p.Pro577=)
c.1611T>C (p.Pro537=)
c.1527T>C (p.Pro509=)
c.625T>C
c.1824T>C (p.Pro608=)
c.1413T>C (p.Pro471=)
n.1726T>C
5g.177095633T>GCA447725628FGFR4c.1731T>G (p.Pro577=)
c.1611T>G (p.Pro537=)
c.1527T>G (p.Pro509=)
c.625T>G
c.1824T>G (p.Pro608=)
c.1413T>G (p.Pro471=)
n.1726T>G
5g.177095633_177095634insGCA2676683416FGFR4c.1731_1732insG (p.Arg578AlafsTer4)
c.1611_1612insG (p.Arg538AlafsTer4)
c.1527_1528insG (p.Arg510AlafsTer4)
c.625_626insG
c.1824_1825insG (p.Arg609AlafsTer4)
c.1413_1414insG (p.Arg472AlafsTer4)
n.1726_1727insG
 gnomAD v4
5g.177095634C>ACA447725630FGFR4c.1732C>A (p.Arg578=)
c.1612C>A (p.Arg538=)
c.1528C>A (p.Arg510=)
c.626C>A
c.1825C>A (p.Arg609=)
c.1414C>A (p.Arg472=)
n.1727C>A
 dbSNP gnomAD v4
5g.177095634C=CA1603404350FGFR4c.1732C= (p.Arg578=)
c.1612C= (p.Arg538=)
c.1528C= (p.Arg510=)
c.626C=
c.1825C= (p.Arg609=)
c.1414C= (p.Arg472=)
n.1727C=
5g.177095634C>GCA362297241FGFR4c.1732C>G (p.Arg578Gly)
c.1612C>G (p.Arg538Gly)
c.1528C>G (p.Arg510Gly)
c.626C>G
c.1825C>G (p.Arg609Gly)
c.1414C>G (p.Arg472Gly)
n.1727C>G
 dbSNP gnomAD v3 gnomAD v4
5g.177095634C>TCA3576541FGFR4c.1732C>T (p.Arg578Trp)
c.1612C>T (p.Arg538Trp)
c.1528C>T (p.Arg510Trp)
c.626C>T
c.1825C>T (p.Arg609Trp)
c.1414C>T (p.Arg472Trp)
n.1727C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177095635G>ACA3576542FGFR4c.1733G>A (p.Arg578Gln)
c.1613G>A (p.Arg538Gln)
c.1529G>A (p.Arg510Gln)
c.627G>A
c.1826G>A (p.Arg609Gln)
c.1415G>A (p.Arg472Gln)
n.1728G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
5g.177095635G>CCA362297242FGFR4c.1733G>C (p.Arg578Pro)
c.1613G>C (p.Arg538Pro)
c.1529G>C (p.Arg510Pro)
c.627G>C
c.1826G>C (p.Arg609Pro)
c.1415G>C (p.Arg472Pro)
n.1728G>C
5g.177095635G=CA1603404351FGFR4c.1733G= (p.Arg578=)
c.1613G= (p.Arg538=)
c.1529G= (p.Arg510=)
c.627G=
c.1826G= (p.Arg609=)
c.1415G= (p.Arg472=)
n.1728G=
5g.177095635G>TCA362297243FGFR4c.1733G>T (p.Arg578Leu)
c.1613G>T (p.Arg538Leu)
c.1529G>T (p.Arg510Leu)
c.627G>T
c.1826G>T (p.Arg609Leu)
c.1415G>T (p.Arg472Leu)
n.1728G>T
5g.177095636G>ACA447725633FGFR4c.1734G>A (p.Arg578=)
c.1614G>A (p.Arg538=)
c.1530G>A (p.Arg510=)
c.628G>A
c.1827G>A (p.Arg609=)
c.1416G>A (p.Arg472=)
n.1729G>A
 gnomAD v4
5g.177095636G>CCA447725635FGFR4c.1734G>C (p.Arg578=)
c.1614G>C (p.Arg538=)
c.1530G>C (p.Arg510=)
c.628G>C
c.1827G>C (p.Arg609=)
c.1416G>C (p.Arg472=)
n.1729G>C
 dbSNP
5g.177095636G>TCA447725636FGFR4c.1734G>T (p.Arg578=)
c.1614G>T (p.Arg538=)
c.1530G>T (p.Arg510=)
c.628G>T
c.1827G>T (p.Arg609=)
c.1416G>T (p.Arg472=)
n.1729G>T
5g.177095637A>CCA362297245FGFR4c.1735A>C (p.Ser579Arg)
c.1615A>C (p.Ser539Arg)
c.1531A>C (p.Ser511Arg)
c.629A>C
c.1828A>C (p.Ser610Arg)
c.1417A>C (p.Ser473Arg)
n.1730A>C
5g.177095637A>GCA362297246FGFR4c.1735A>G (p.Ser579Gly)
c.1615A>G (p.Ser539Gly)
c.1531A>G (p.Ser511Gly)
c.629A>G
c.1828A>G (p.Ser610Gly)
c.1417A>G (p.Ser473Gly)
n.1730A>G
5g.177095637A>TCA362297244FGFR4c.1735A>T (p.Ser579Cys)
c.1615A>T (p.Ser539Cys)
c.1531A>T (p.Ser511Cys)
c.629A>T
c.1828A>T (p.Ser610Cys)
c.1417A>T (p.Ser473Cys)
n.1730A>T
5g.177095638G>ACA362297247FGFR4c.1736G>A (p.Ser579Asn)
c.1616G>A (p.Ser539Asn)
c.1532G>A (p.Ser511Asn)
c.630G>A
c.1829G>A (p.Ser610Asn)
c.1418G>A (p.Ser473Asn)
n.1731G>A
 dbSNP
5g.177095638G>CCA362297248FGFR4c.1736G>C (p.Ser579Thr)
c.1616G>C (p.Ser539Thr)
c.1532G>C (p.Ser511Thr)
c.630G>C
c.1829G>C (p.Ser610Thr)
c.1418G>C (p.Ser473Thr)
n.1731G>C
5g.177095638G>TCA362297249FGFR4c.1736G>T (p.Ser579Ile)
c.1616G>T (p.Ser539Ile)
c.1532G>T (p.Ser511Ile)
c.630G>T
c.1829G>T (p.Ser610Ile)
c.1418G>T (p.Ser473Ile)
n.1731G>T
5g.177095639C>ACA3576544FGFR4c.1737C>A (p.Ser579Arg)
c.1617C>A (p.Ser539Arg)
c.1533C>A (p.Ser511Arg)
c.631C>A
c.1830C>A (p.Ser610Arg)
c.1419C>A (p.Ser473Arg)
n.1732C>A
 dbSNP ExAC gnomAD v2 gnomAD v4
5g.177095639C=CA1603404352FGFR4c.1737C= (p.Ser579=)
c.1617C= (p.Ser539=)
c.1533C= (p.Ser511=)
c.631C=
c.1830C= (p.Ser610=)
c.1419C= (p.Ser473=)
n.1732C=
5g.177095639C>GCA362297250FGFR4c.1737C>G (p.Ser579Arg)
c.1617C>G (p.Ser539Arg)
c.1533C>G (p.Ser511Arg)
c.631C>G
c.1830C>G (p.Ser610Arg)
c.1419C>G (p.Ser473Arg)
n.1732C>G
5g.177095639C>TCA3576543FGFR4c.1737C>T (p.Ser579=)
c.1617C>T (p.Ser539=)
c.1533C>T (p.Ser511=)
c.631C>T
c.1830C>T (p.Ser610=)
c.1419C>T (p.Ser473=)
n.1732C>T
 dbSNP ExAC gnomAD v2
5g.177095640A>CCA362297253FGFR4c.1738A>C (p.Ser580Arg)
c.1618A>C (p.Ser540Arg)
c.1534A>C (p.Ser512Arg)
c.632A>C
c.1831A>C (p.Ser611Arg)
c.1420A>C (p.Ser474Arg)
n.1733A>C
5g.177095640A>GCA362297251FGFR4c.1738A>G (p.Ser580Gly)
c.1618A>G (p.Ser540Gly)
c.1534A>G (p.Ser512Gly)
c.632A>G
c.1831A>G (p.Ser611Gly)
c.1420A>G (p.Ser474Gly)
n.1733A>G
5g.177095640A>TCA362297252FGFR4c.1738A>T (p.Ser580Cys)
c.1618A>T (p.Ser540Cys)
c.1534A>T (p.Ser512Cys)
c.632A>T
c.1831A>T (p.Ser611Cys)
c.1420A>T (p.Ser474Cys)
n.1733A>T
5g.177095641G>ACA132833278FGFR4c.1739G>A (p.Ser580Asn)
c.1619G>A (p.Ser540Asn)
c.1535G>A (p.Ser512Asn)
c.633G>A
c.1832G>A (p.Ser611Asn)
c.1421G>A (p.Ser474Asn)
n.1734G>A
 dbSNP
5g.177095641G>CCA362297254FGFR4c.1739G>C (p.Ser580Thr)
c.1619G>C (p.Ser540Thr)
c.1535G>C (p.Ser512Thr)
c.633G>C
c.1832G>C (p.Ser611Thr)
c.1421G>C (p.Ser474Thr)
n.1734G>C
5g.177095641G=CA1603404353FGFR4c.1739G= (p.Ser580=)
c.1619G= (p.Ser540=)
c.1535G= (p.Ser512=)
c.633G=
c.1832G= (p.Ser611=)
c.1421G= (p.Ser474=)
n.1734G=
5g.177095641G>TCA362297255FGFR4c.1739G>T (p.Ser580Ile)
c.1619G>T (p.Ser540Ile)
c.1535G>T (p.Ser512Ile)
c.633G>T
c.1832G>T (p.Ser611Ile)
c.1421G>T (p.Ser474Ile)
n.1734G>T
 COSMIC COSMIC
5g.177095642T>ACA362297256FGFR4c.1740T>A (p.Ser580Arg)
c.1620T>A (p.Ser540Arg)
c.1536T>A (p.Ser512Arg)
c.634T>A
c.1833T>A (p.Ser611Arg)
c.1422T>A (p.Ser474Arg)
n.1735T>A
5g.177095642T>CCA447725640FGFR4c.1740T>C (p.Ser580=)
c.1620T>C (p.Ser540=)
c.1536T>C (p.Ser512=)
c.634T>C
c.1833T>C (p.Ser611=)
c.1422T>C (p.Ser474=)
n.1735T>C
 dbSNP gnomAD v2 gnomAD v4
5g.177095642T>GCA362297257FGFR4c.1740T>G (p.Ser580Arg)
c.1620T>G (p.Ser540Arg)
c.1536T>G (p.Ser512Arg)
c.634T>G
c.1833T>G (p.Ser611Arg)
c.1422T>G (p.Ser474Arg)
n.1735T>G
5g.177095642T=CA1603404354FGFR4c.1740T= (p.Ser580=)
c.1620T= (p.Ser540=)
c.1536T= (p.Ser512=)
c.634T=
c.1833T= (p.Ser611=)
c.1422T= (p.Ser474=)
n.1735T=
5g.177095643G>ACA362297258FGFR4c.1741G>A (p.Glu581Lys)
c.1621G>A (p.Glu541Lys)
c.1537G>A (p.Glu513Lys)
c.635G>A
c.1834G>A (p.Glu612Lys)
c.1423G>A (p.Glu475Lys)
n.1736G>A
5g.177095643G>CCA362297260FGFR4c.1741G>C (p.Glu581Gln)
c.1621G>C (p.Glu541Gln)
c.1537G>C (p.Glu513Gln)
c.635G>C
c.1834G>C (p.Glu612Gln)
c.1423G>C (p.Glu475Gln)
n.1736G>C
5g.177095643G>TCA362297259FGFR4c.1741G>T (p.Glu581Ter)
c.1621G>T (p.Glu541Ter)
c.1537G>T (p.Glu513Ter)
c.635G>T
c.1834G>T (p.Glu612Ter)
c.1423G>T (p.Glu475Ter)
n.1736G>T
5g.177095644A>CCA362297261FGFR4c.1742A>C (p.Glu581Ala)
c.1622A>C (p.Glu541Ala)
c.1538A>C (p.Glu513Ala)
c.636A>C
c.1835A>C (p.Glu612Ala)
c.1424A>C (p.Glu475Ala)
n.1737A>C
5g.177095644A>GCA362297262FGFR4c.1742A>G (p.Glu581Gly)
c.1622A>G (p.Glu541Gly)
c.1538A>G (p.Glu513Gly)
c.636A>G
c.1835A>G (p.Glu612Gly)
c.1424A>G (p.Glu475Gly)
n.1737A>G
 gnomAD v3 gnomAD v4
5g.177095644A>TCA362297263FGFR4c.1742A>T (p.Glu581Val)
c.1622A>T (p.Glu541Val)
c.1538A>T (p.Glu513Val)
c.636A>T
c.1835A>T (p.Glu612Val)
c.1424A>T (p.Glu475Val)
n.1737A>T
5g.177095644_177095645delinsAGCA1603404355FGFR4c.1742_1743delinsAG (p.Glu581=)
c.1622_1623delinsAG (p.Glu541=)
c.1538_1539delinsAG (p.Glu513=)
c.636_637delinsAG
c.1835_1836delinsAG (p.Glu612=)
c.1424_1425delinsAG (p.Glu475=)
n.1737_1738delinsAG
5g.177095645G>ACA3576545FGFR4c.1743G>A (p.Glu581=)
c.1623G>A (p.Glu541=)
c.1539G>A (p.Glu513=)
c.637G>A
c.1836G>A (p.Glu612=)
c.1425G>A (p.Glu475=)
n.1738G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177095645G>CCA362297264FGFR4c.1743G>C (p.Glu581Asp)
c.1623G>C (p.Glu541Asp)
c.1539G>C (p.Glu513Asp)
c.637G>C
c.1836G>C (p.Glu612Asp)
c.1425G>C (p.Glu475Asp)
n.1738G>C
5g.177095645G=CA1603404356FGFR4c.1743G= (p.Glu581=)
c.1623G= (p.Glu541=)
c.1539G= (p.Glu513=)
c.637G=
c.1836G= (p.Glu612=)
c.1425G= (p.Glu475=)
n.1738G=
5g.177095645G>TCA362297265FGFR4c.1743G>T (p.Glu581Asp)
c.1623G>T (p.Glu541Asp)
c.1539G>T (p.Glu513Asp)
c.637G>T
c.1836G>T (p.Glu612Asp)
c.1425G>T (p.Glu475Asp)
n.1738G>T
 gnomAD v4
5g.177095648delCA808060602FGFR4c.1746del (p.Pro583ArgfsTer?)
c.1626del (p.Pro543ArgfsTer?)
c.1542del (p.Pro515ArgfsTer?)
c.640del
c.1839del (p.Pro614ArgfsTer?)
c.1428del (p.Pro477ArgfsTer?)
n.1741del
 dbSNP gnomAD v4
5g.177095646G>ACA362297266FGFR4c.1744G>A (p.Gly582Arg)
c.1624G>A (p.Gly542Arg)
c.1540G>A (p.Gly514Arg)
c.638G>A
c.1837G>A (p.Gly613Arg)
c.1426G>A (p.Gly476Arg)
n.1739G>A
 gnomAD v4
5g.177095646G>CCA362297267FGFR4c.1744G>C (p.Gly582Arg)
c.1624G>C (p.Gly542Arg)
c.1540G>C (p.Gly514Arg)
c.638G>C
c.1837G>C (p.Gly613Arg)
c.1426G>C (p.Gly476Arg)
n.1739G>C
5g.177095646G=CA1603404357FGFR4c.1744G= (p.Gly582=)
c.1624G= (p.Gly542=)
c.1540G= (p.Gly514=)
c.638G=
c.1837G= (p.Gly613=)
c.1426G= (p.Gly476=)
n.1739G=
5g.177095646G>TCA3576546FGFR4c.1744G>T (p.Gly582Trp)
c.1624G>T (p.Gly542Trp)
c.1540G>T (p.Gly514Trp)
c.638G>T
c.1837G>T (p.Gly613Trp)
c.1426G>T (p.Gly476Trp)
n.1739G>T
 dbSNP ExAC gnomAD v2 gnomAD v4
5g.177095646_177095649dupCA2676683417FGFR4c.1744_1747dup (p.Pro583ArgfsTer?)
c.1624_1627dup (p.Pro543ArgfsTer?)
c.1540_1543dup (p.Pro515ArgfsTer?)
c.638_641dup
c.1837_1840dup (p.Pro614ArgfsTer?)
c.1426_1429dup (p.Pro477ArgfsTer?)
n.1739_1742dup
 gnomAD v4
5g.177095646_177095650delinsGGGCCCA1603404358FGFR4c.1744_1748delinsGGGCC (p.Gly582=)
c.1624_1628delinsGGGCC (p.Gly542=)
c.1540_1544delinsGGGCC (p.Gly514=)
c.638_642delinsGGGCC
c.1837_1841delinsGGGCC (p.Gly613=)
c.1426_1430delinsGGGCC (p.Gly476=)
n.1739_1743delinsGGGCC
5g.177095647G>ACA362297268FGFR4c.1745G>A (p.Gly582Glu)
c.1625G>A (p.Gly542Glu)
c.1541G>A (p.Gly514Glu)
c.639G>A
c.1838G>A (p.Gly613Glu)
c.1427G>A (p.Gly476Glu)
n.1740G>A
 dbSNP gnomAD v4
5g.177095647G>CCA362297269FGFR4c.1745G>C (p.Gly582Ala)
c.1625G>C (p.Gly542Ala)
c.1541G>C (p.Gly514Ala)
c.639G>C
c.1838G>C (p.Gly613Ala)
c.1427G>C (p.Gly476Ala)
n.1740G>C
5g.177095647G=CA1603404359FGFR4c.1745G= (p.Gly582=)
c.1625G= (p.Gly542=)
c.1541G= (p.Gly514=)
c.639G=
c.1838G= (p.Gly613=)
c.1427G= (p.Gly476=)
n.1740G=
5g.177095647G>TCA362297270FGFR4c.1745G>T (p.Gly582Val)
c.1625G>T (p.Gly542Val)
c.1541G>T (p.Gly514Val)
c.639G>T
c.1838G>T (p.Gly613Val)
c.1427G>T (p.Gly476Val)
n.1740G>T
5g.177095648_177095651delCA564898789FGFR4c.1746_1749del (p.Pro583SerfsTer?)
c.1626_1629del (p.Pro543SerfsTer?)
c.1542_1545del (p.Pro515SerfsTer?)
c.640_643del
c.1839_1842del (p.Pro614SerfsTer?)
c.1428_1431del (p.Pro477SerfsTer?)
n.1741_1744del
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.177095648G>ACA447725645FGFR4c.1746G>A (p.Gly582=)
c.1626G>A (p.Gly542=)
c.1542G>A (p.Gly514=)
c.640G>A
c.1839G>A (p.Gly613=)
c.1428G>A (p.Gly476=)
n.1741G>A
 dbSNP
5g.177095648G>CCA447725648FGFR4c.1746G>C (p.Gly582=)
c.1626G>C (p.Gly542=)
c.1542G>C (p.Gly514=)
c.640G>C
c.1839G>C (p.Gly613=)
c.1428G>C (p.Gly476=)
n.1741G>C
5g.177095648G>TCA447725649FGFR4c.1746G>T (p.Gly582=)
c.1626G>T (p.Gly542=)
c.1542G>T (p.Gly514=)
c.640G>T
c.1839G>T (p.Gly613=)
c.1428G>T (p.Gly476=)
n.1741G>T
 gnomAD v4
5g.177095649C>ACA362297271FGFR4c.1747C>A (p.Pro583Thr)
c.1627C>A (p.Pro543Thr)
c.1543C>A (p.Pro515Thr)
c.641C>A
c.1840C>A (p.Pro614Thr)
c.1429C>A (p.Pro477Thr)
n.1742C>A
 dbSNP
5g.177095649C>GCA362297273FGFR4c.1747C>G (p.Pro583Ala)
c.1627C>G (p.Pro543Ala)
c.1543C>G (p.Pro515Ala)
c.641C>G
c.1840C>G (p.Pro614Ala)
c.1429C>G (p.Pro477Ala)
n.1742C>G
5g.177095649C>TCA362297272FGFR4c.1747C>T (p.Pro583Ser)
c.1627C>T (p.Pro543Ser)
c.1543C>T (p.Pro515Ser)
c.641C>T
c.1840C>T (p.Pro614Ser)
c.1429C>T (p.Pro477Ser)
n.1742C>T
 dbSNP
5g.177095650C>ACA362297274FGFR4c.1748C>A (p.Pro583Gln)
c.1628C>A (p.Pro543Gln)
c.1544C>A (p.Pro515Gln)
c.642C>A
c.1841C>A (p.Pro614Gln)
c.1430C>A (p.Pro477Gln)
n.1743C>A
 dbSNP gnomAD v4 COSMIC COSMIC
5g.177095650C=CA1603404360FGFR4c.1748C= (p.Pro583=)
c.1628C= (p.Pro543=)
c.1544C= (p.Pro515=)
c.642C=
c.1841C= (p.Pro614=)
c.1430C= (p.Pro477=)
n.1743C=
5g.177095650C>GCA362297275FGFR4c.1748C>G (p.Pro583Arg)
c.1628C>G (p.Pro543Arg)
c.1544C>G (p.Pro515Arg)
c.642C>G
c.1841C>G (p.Pro614Arg)
c.1430C>G (p.Pro477Arg)
n.1743C>G
5g.177095650C>TCA3576547FGFR4c.1748C>T (p.Pro583Leu)
c.1628C>T (p.Pro543Leu)
c.1544C>T (p.Pro515Leu)
c.642C>T
c.1841C>T (p.Pro614Leu)
c.1430C>T (p.Pro477Leu)
n.1743C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.177095651G>ACA3576548FGFR4c.1749G>A (p.Pro583=)
c.1629G>A (p.Pro543=)
c.1545G>A (p.Pro515=)
c.643G>A
c.1842G>A (p.Pro614=)
c.1431G>A (p.Pro477=)
n.1744G>A
 dbSNP ExAC gnomAD v2 gnomAD v4
5g.177095651G>CCA447725652FGFR4c.1749G>C (p.Pro583=)
c.1629G>C (p.Pro543=)
c.1545G>C (p.Pro515=)
c.643G>C
c.1842G>C (p.Pro614=)
c.1431G>C (p.Pro477=)
n.1744G>C
 gnomAD v4
5g.177095651G=CA1603404361FGFR4c.1749G= (p.Pro583=)
c.1629G= (p.Pro543=)
c.1545G= (p.Pro515=)
c.643G=
c.1842G= (p.Pro614=)
c.1431G= (p.Pro477=)
n.1744G=
5g.177095651G>TCA447725654FGFR4c.1749G>T (p.Pro583=)
c.1629G>T (p.Pro543=)
c.1545G>T (p.Pro515=)
c.643G>T
c.1842G>T (p.Pro614=)
c.1431G>T (p.Pro477=)
n.1744G>T
 gnomAD v4
5g.177095652C>ACA362297276FGFR4c.1750C>A (p.Leu584Ile)
c.1630C>A (p.Leu544Ile)
c.1546C>A (p.Leu516Ile)
c.644C>A
c.1843C>A (p.Leu615Ile)
c.1432C>A (p.Leu478Ile)
n.1745C>A
5g.177095652C=CA1603404362FGFR4c.1750C= (p.Leu584=)
c.1630C= (p.Leu544=)
c.1546C= (p.Leu516=)
c.644C=
c.1843C= (p.Leu615=)
c.1432C= (p.Leu478=)
n.1745C=
5g.177095652C>GCA362297277FGFR4c.1750C>G (p.Leu584Val)
c.1630C>G (p.Leu544Val)
c.1546C>G (p.Leu516Val)
c.644C>G
c.1843C>G (p.Leu615Val)
c.1432C>G (p.Leu478Val)
n.1745C>G
5g.177095652C>TCA362297278FGFR4c.1750C>T (p.Leu584Phe)
c.1630C>T (p.Leu544Phe)
c.1546C>T (p.Leu516Phe)
c.644C>T
c.1843C>T (p.Leu615Phe)
c.1432C>T (p.Leu478Phe)
n.1745C>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.177095653T>ACA362297279FGFR4c.1751T>A (p.Leu584His)
c.1631T>A (p.Leu544His)
c.1547T>A (p.Leu516His)
c.645T>A
c.1844T>A (p.Leu615His)
c.1433T>A (p.Leu478His)
n.1746T>A
5g.177095653T>CCA362297280FGFR4c.1751T>C (p.Leu584Pro)
c.1631T>C (p.Leu544Pro)
c.1547T>C (p.Leu516Pro)
c.645T>C
c.1844T>C (p.Leu615Pro)
c.1433T>C (p.Leu478Pro)
n.1746T>C
 dbSNP gnomAD v3 gnomAD v4
5g.177095653T>GCA362297281FGFR4c.1751T>G (p.Leu584Arg)
c.1631T>G (p.Leu544Arg)
c.1547T>G (p.Leu516Arg)
c.645T>G
c.1844T>G (p.Leu615Arg)
c.1433T>G (p.Leu478Arg)
n.1746T>G
5g.177095653T=CA1603404363FGFR4c.1751T= (p.Leu584=)
c.1631T= (p.Leu544=)
c.1547T= (p.Leu516=)
c.645T=
c.1844T= (p.Leu615=)
c.1433T= (p.Leu478=)
n.1746T=

Number of alleles fetched