Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.1801409T>ACA355974913FGFR3c.488T>A (p.Leu163Gln)
c.476T>A (p.Leu159Gln)
n.744T>A
n.763T>A
4g.1801409T>CCA355974911FGFR3c.488T>C (p.Leu163Pro)
c.476T>C (p.Leu159Pro)
n.744T>C
n.763T>C
4g.1801409T>GCA355974910FGFR3c.488T>G (p.Leu163Arg)
c.476T>G (p.Leu159Arg)
n.744T>G
n.763T>G
4g.1801410G>ACA438062752FGFR3c.489G>A (p.Leu163=)
c.477G>A (p.Leu159=)
n.745G>A
n.764G>A
 dbSNP gnomAD v4
4g.1801410G>CCA438062753FGFR3c.489G>C (p.Leu163=)
c.477G>C (p.Leu159=)
n.745G>C
n.764G>C
4g.1801410G=CA1433504804FGFR3c.489G= (p.Leu163=)
c.477G= (p.Leu159=)
n.745G=
n.764G=
4g.1801410G>TCA438062754FGFR3c.489G>T (p.Leu163=)
c.477G>T (p.Leu159=)
n.745G>T
n.764G>T
 gnomAD v4
4g.1801411C>ACA355974915FGFR3c.490C>A (p.Leu164Met)
c.478C>A (p.Leu160Met)
n.746C>A
n.765C>A
 gnomAD v4
4g.1801411C=CA1433504805FGFR3c.490C= (p.Leu164=)
c.478C= (p.Leu160=)
n.746C=
n.765C=
4g.1801411C>GCA2809859FGFR3c.490C>G (p.Leu164Val)
c.478C>G (p.Leu160Val)
n.746C>G
n.765C>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.1801411C>TCA438062755FGFR3c.490C>T (p.Leu164=)
c.478C>T (p.Leu160=)
n.746C>T
n.765C>T
 dbSNP gnomAD v2 gnomAD v4
4g.1801412T>ACA355974917FGFR3c.491T>A (p.Leu164Gln)
c.479T>A (p.Leu160Gln)
n.747T>A
n.766T>A
 gnomAD v4
4g.1801412T>CCA355974918FGFR3c.491T>C (p.Leu164Pro)
c.479T>C (p.Leu160Pro)
n.747T>C
n.766T>C
 gnomAD v4
4g.1801412T>GCA355974920FGFR3c.491T>G (p.Leu164Arg)
c.479T>G (p.Leu160Arg)
n.747T>G
n.766T>G
4g.1801413G>ACA438062756FGFR3c.492G>A (p.Leu164=)
c.480G>A (p.Leu160=)
n.748G>A
n.767G>A
 gnomAD v4
4g.1801413G>CCA438062757FGFR3c.492G>C (p.Leu164=)
c.480G>C (p.Leu160=)
n.748G>C
n.767G>C
4g.1801413G>TCA438062758FGFR3c.492G>T (p.Leu164=)
c.480G>T (p.Leu160=)
n.748G>T
n.767G>T
 gnomAD v4
4g.1801414G>ACA355974925FGFR3c.493G>A (p.Ala165Thr)
c.481G>A (p.Ala161Thr)
n.749G>A
n.768G>A
 dbSNP gnomAD v2 gnomAD v4
4g.1801414G>CCA355974923FGFR3c.493G>C (p.Ala165Pro)
c.481G>C (p.Ala161Pro)
n.749G>C
n.768G>C
4g.1801414G=CA1433504806FGFR3c.493G= (p.Ala165=)
c.481G= (p.Ala161=)
n.749G=
n.768G=
4g.1801414G>TCA355974921FGFR3c.493G>T (p.Ala165Ser)
c.481G>T (p.Ala161Ser)
n.749G>T
n.768G>T
 gnomAD v4
4g.1801415C>ACA355974928FGFR3c.494C>A (p.Ala165Asp)
c.482C>A (p.Ala161Asp)
n.750C>A
n.769C>A
 gnomAD v4
4g.1801415C>GCA355974929FGFR3c.494C>G (p.Ala165Gly)
c.482C>G (p.Ala161Gly)
n.750C>G
n.769C>G
4g.1801415C>TCA355974930FGFR3c.494C>T (p.Ala165Val)
c.482C>T (p.Ala161Val)
n.750C>T
n.769C>T
 dbSNP gnomAD v4 COSMIC COSMIC
4g.1801416C>ACA438062759FGFR3c.495C>A (p.Ala165=)
c.483C>A (p.Ala161=)
n.751C>A
n.770C>A
 dbSNP gnomAD v4
4g.1801416C=CA1433504807FGFR3c.495C= (p.Ala165=)
c.483C= (p.Ala161=)
n.751C=
n.770C=
4g.1801416C>GCA438062760FGFR3c.495C>G (p.Ala165=)
c.483C>G (p.Ala161=)
n.751C>G
n.770C>G
4g.1801416C>TCA91249097FGFR3c.495C>T (p.Ala165=)
c.483C>T (p.Ala161=)
n.751C>T
n.770C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
4g.1801417G>ACA355974932FGFR3c.496G>A (p.Val166Met)
c.484G>A (p.Val162Met)
n.752G>A
n.771G>A
 dbSNP gnomAD v2 gnomAD v4
4g.1801417G>CCA355974934FGFR3c.496G>C (p.Val166Leu)
c.484G>C (p.Val162Leu)
n.752G>C
n.771G>C
4g.1801417G=CA1433504808FGFR3c.496G= (p.Val166=)
c.484G= (p.Val162=)
n.752G=
n.771G=
4g.1801417G>TCA355974936FGFR3c.496G>T (p.Val166Leu)
c.484G>T (p.Val162Leu)
n.752G>T
n.771G>T
 gnomAD v4
4g.1801417_1801419delCA2760148312FGFR3c.496_498del (p.Val166del)
c.484_486del (p.Val162del)
n.752_754del
n.771_773del
4g.1801418T>ACA355974938FGFR3c.497T>A (p.Val166Glu)
c.485T>A (p.Val162Glu)
n.753T>A
n.772T>A
4g.1801418T>CCA355974941FGFR3c.497T>C (p.Val166Ala)
c.485T>C (p.Val162Ala)
n.753T>C
n.772T>C
4g.1801418T>GCA355974939FGFR3c.497T>G (p.Val166Gly)
c.485T>G (p.Val162Gly)
n.753T>G
n.772T>G
 dbSNP
4g.1801419G>ACA438062761FGFR3c.498G>A (p.Val166=)
c.486G>A (p.Val162=)
n.754G>A
n.773G>A
 dbSNP gnomAD v4
4g.1801419G>CCA438062763FGFR3c.498G>C (p.Val166=)
c.486G>C (p.Val162=)
n.754G>C
n.773G>C
 dbSNP
4g.1801419G>TCA438062762FGFR3c.498G>T (p.Val166=)
c.486G>T (p.Val162=)
n.754G>T
n.773G>T
 gnomAD v4
4g.1801420C>ACA355974943FGFR3c.499C>A (p.Pro167Thr)
c.487C>A (p.Pro163Thr)
n.755C>A
n.774C>A
4g.1801420C>GCA355974944FGFR3c.499C>G (p.Pro167Ala)
c.487C>G (p.Pro163Ala)
n.755C>G
n.774C>G
4g.1801420C>TCA355974946FGFR3c.499C>T (p.Pro167Ser)
c.487C>T (p.Pro163Ser)
n.755C>T
n.774C>T
 dbSNP gnomAD v4
4g.1801421C>ACA355974948FGFR3c.500C>A (p.Pro167Gln)
c.488C>A (p.Pro163Gln)
n.756C>A
n.775C>A
 gnomAD v4
4g.1801421C>GCA355974949FGFR3c.500C>G (p.Pro167Arg)
c.488C>G (p.Pro163Arg)
n.756C>G
n.775C>G
4g.1801421C>TCA355974951FGFR3c.500C>T (p.Pro167Leu)
c.488C>T (p.Pro163Leu)
n.756C>T
n.775C>T
 gnomAD v4
4g.1801422G>ACA91249100FGFR3c.501G>A (p.Pro167=)
c.489G>A (p.Pro163=)
n.757G>A
n.776G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.1801422G>CCA438062765FGFR3c.501G>C (p.Pro167=)
c.489G>C (p.Pro163=)
n.757G>C
n.776G>C
4g.1801422G=CA1433504809FGFR3c.501G= (p.Pro167=)
c.489G= (p.Pro163=)
n.757G=
n.776G=
4g.1801422G>TCA438062764FGFR3c.501G>T (p.Pro167=)
c.489G>T (p.Pro163=)
n.757G>T
n.776G>T
4g.1801423G>ACA355974954FGFR3c.502G>A (p.Ala168Thr)
c.490G>A (p.Ala164Thr)
n.758G>A
n.777G>A
 dbSNP gnomAD v4
4g.1801423G>CCA355974956FGFR3c.502G>C (p.Ala168Pro)
c.490G>C (p.Ala164Pro)
n.758G>C
n.777G>C
 dbSNP
4g.1801423G>TCA355974958FGFR3c.502G>T (p.Ala168Ser)
c.490G>T (p.Ala164Ser)
n.758G>T
n.777G>T
4g.1801424C>ACA355974960FGFR3c.503C>A (p.Ala168Asp)
c.491C>A (p.Ala164Asp)
n.759C>A
n.778C>A
 gnomAD v4
4g.1801424C>GCA355974963FGFR3c.503C>G (p.Ala168Gly)
c.491C>G (p.Ala164Gly)
n.759C>G
n.778C>G
4g.1801424C>TCA355974962FGFR3c.503C>T (p.Ala168Val)
c.491C>T (p.Ala164Val)
n.759C>T
n.778C>T
 dbSNP gnomAD v4
4g.1801428_1801440dupCA2669560527FGFR3c.507_519dup (p.Phe174GlnfsTer?)
c.495_507dup (p.Phe170GlnfsTer?)
n.763_775dup
n.782_794dup
 gnomAD v4
4g.1801425C>ACA438062767FGFR3c.504C>A (p.Ala168=)
c.492C>A (p.Ala164=)
n.760C>A
n.779C>A
 dbSNP gnomAD v4
4g.1801425C=CA1433504810FGFR3c.504C= (p.Ala168=)
c.492C= (p.Ala164=)
n.760C=
n.779C=
4g.1801425C>GCA438062766FGFR3c.504C>G (p.Ala168=)
c.492C>G (p.Ala164=)
n.760C>G
n.779C>G
4g.1801425C>TCA2809860FGFR3c.504C>T (p.Ala168=)
c.492C>T (p.Ala164=)
n.760C>T
n.779C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.1801426G>ACA355974965FGFR3c.505G>A (p.Ala169Thr)
c.493G>A (p.Ala165Thr)
n.761G>A
n.780G>A
 dbSNP gnomAD v2 gnomAD v4
4g.1801426G>CCA355974964FGFR3c.505G>C (p.Ala169Pro)
c.493G>C (p.Ala165Pro)
n.761G>C
n.780G>C
 gnomAD v4
4g.1801426G=CA1433504811FGFR3c.505G= (p.Ala169=)
c.493G= (p.Ala165=)
n.761G=
n.780G=
4g.1801426G>TCA355974967FGFR3c.505G>T (p.Ala169Ser)
c.493G>T (p.Ala165Ser)
n.761G>T
n.780G>T
 gnomAD v4
4g.1801427C>ACA355974968FGFR3c.506C>A (p.Ala169Asp)
c.494C>A (p.Ala165Asp)
n.762C>A
n.781C>A
4g.1801427C>GCA355974971FGFR3c.506C>G (p.Ala169Gly)
c.494C>G (p.Ala165Gly)
n.762C>G
n.781C>G
4g.1801427C>TCA355974969FGFR3c.506C>T (p.Ala169Val)
c.494C>T (p.Ala165Val)
n.762C>T
n.781C>T
 gnomAD v4
4g.1801428C>ACA438062769FGFR3c.507C>A (p.Ala169=)
c.495C>A (p.Ala165=)
n.763C>A
n.782C>A
 gnomAD v4
4g.1801428C=CA1433504812FGFR3c.507C= (p.Ala169=)
c.495C= (p.Ala165=)
n.763C=
n.782C=
4g.1801428C>GCA438062770FGFR3c.507C>G (p.Ala169=)
c.495C>G (p.Ala165=)
n.763C>G
n.782C>G
 dbSNP gnomAD v2 gnomAD v4
4g.1801428C>TCA438062768FGFR3c.507C>T (p.Ala169=)
c.495C>T (p.Ala165=)
n.763C>T
n.782C>T
 dbSNP gnomAD v2 gnomAD v4
4g.1801429A=CA1433504813FGFR3c.508A= (p.Asn170=)
c.496A= (p.Asn166=)
n.764A=
n.783A=
4g.1801429A>CCA355974972FGFR3c.508A>C (p.Asn170His)
c.496A>C (p.Asn166His)
n.764A>C
n.783A>C
4g.1801429A>GCA355974975FGFR3c.508A>G (p.Asn170Asp)
c.496A>G (p.Asn166Asp)
n.764A>G
n.783A>G
4g.1801429A>TCA355974974FGFR3c.508A>T (p.Asn170Tyr)
c.496A>T (p.Asn166Tyr)
n.764A>T
n.783A>T
 dbSNP gnomAD v3 gnomAD v4
4g.1801430A>CCA355974978FGFR3c.509A>C (p.Asn170Thr)
c.497A>C (p.Asn166Thr)
n.765A>C
n.784A>C
4g.1801430A>GCA355974981FGFR3c.509A>G (p.Asn170Ser)
c.497A>G (p.Asn166Ser)
n.765A>G
n.784A>G
4g.1801430A>TCA355974980FGFR3c.509A>T (p.Asn170Ile)
c.497A>T (p.Asn166Ile)
n.765A>T
n.784A>T
4g.1801431C>ACA355974983FGFR3c.510C>A (p.Asn170Lys)
c.498C>A (p.Asn166Lys)
n.766C>A
n.785C>A
4g.1801431C>GCA355974985FGFR3c.510C>G (p.Asn170Lys)
c.498C>G (p.Asn166Lys)
n.766C>G
n.785C>G
4g.1801431C>TCA438062771FGFR3c.510C>T (p.Asn170=)
c.498C>T (p.Asn166=)
n.766C>T
n.785C>T
4g.1801432A=CA1433504814FGFR3c.511A= (p.Thr171=)
c.499A= (p.Thr167=)
n.767A=
n.786A=
4g.1801432A>CCA91249133FGFR3c.511A>C (p.Thr171Pro)
c.499A>C (p.Thr167Pro)
n.767A>C
n.786A>C
 dbSNP gnomAD v4
4g.1801432A>GCA355974988FGFR3c.511A>G (p.Thr171Ala)
c.499A>G (p.Thr167Ala)
n.767A>G
n.786A>G
4g.1801432A>TCA355974989FGFR3c.511A>T (p.Thr171Ser)
c.499A>T (p.Thr167Ser)
n.767A>T
n.786A>T
4g.1801433C>ACA355974991FGFR3c.512C>A (p.Thr171Asn)
c.500C>A (p.Thr167Asn)
n.768C>A
n.787C>A
 gnomAD v4
4g.1801433C>GCA355974992FGFR3c.512C>G (p.Thr171Ser)
c.500C>G (p.Thr167Ser)
n.768C>G
n.787C>G
4g.1801433C>TCA355974993FGFR3c.512C>T (p.Thr171Ile)
c.500C>T (p.Thr167Ile)
n.768C>T
n.787C>T
4g.1801434C>ACA438062772FGFR3c.513C>A (p.Thr171=)
c.501C>A (p.Thr167=)
n.769C>A
n.788C>A
 gnomAD v4
4g.1801434C=CA1433504815FGFR3c.513C= (p.Thr171=)
c.501C= (p.Thr167=)
n.769C=
n.788C=
4g.1801434C>GCA438062773FGFR3c.513C>G (p.Thr171=)
c.501C>G (p.Thr167=)
n.769C>G
n.788C>G
4g.1801434C>TCA2809861FGFR3c.513C>T (p.Thr171=)
c.501C>T (p.Thr167=)
n.769C>T
n.788C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.1801435G>ACA2809862FGFR3c.514G>A (p.Val172Ile)
c.502G>A (p.Val168Ile)
n.770G>A
n.789G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.1801435G>CCA355974997FGFR3c.514G>C (p.Val172Leu)
c.502G>C (p.Val168Leu)
n.770G>C
n.789G>C
4g.1801435G=CA1433504816FGFR3c.514G= (p.Val172=)
c.502G= (p.Val168=)
n.770G=
n.789G=
4g.1801435G>TCA355974999FGFR3c.514G>T (p.Val172Phe)
c.502G>T (p.Val168Phe)
n.770G>T
n.789G>T
 gnomAD v4
4g.1801436T>ACA355975001FGFR3c.515T>A (p.Val172Asp)
c.503T>A (p.Val168Asp)
n.771T>A
n.790T>A
4g.1801436T>CCA355975004FGFR3c.515T>C (p.Val172Ala)
c.503T>C (p.Val168Ala)
n.771T>C
n.790T>C
 gnomAD v4
4g.1801436T>GCA355975003FGFR3c.515T>G (p.Val172Gly)
c.503T>G (p.Val168Gly)
n.771T>G
n.790T>G
4g.1801437C>ACA438062774FGFR3c.516C>A (p.Val172=)
c.504C>A (p.Val168=)
n.772C>A
n.791C>A
4g.1801437C>GCA438062775FGFR3c.516C>G (p.Val172=)
c.504C>G (p.Val168=)
n.772C>G
n.791C>G
 gnomAD v4
4g.1801437C>TCA438062776FGFR3c.516C>T (p.Val172=)
c.504C>T (p.Val168=)
n.772C>T
n.791C>T
 gnomAD v4
4g.1801438C>ACA355975005FGFR3c.517C>A (p.Arg173Ser)
c.505C>A (p.Arg169Ser)
n.773C>A
n.792C>A
 gnomAD v4
4g.1801438C=CA1433504817FGFR3c.517C= (p.Arg173=)
c.505C= (p.Arg169=)
n.773C=
n.792C=
4g.1801438C>GCA355975007FGFR3c.517C>G (p.Arg173Gly)
c.505C>G (p.Arg169Gly)
n.773C>G
n.792C>G
 gnomAD v4
4g.1801438C>TCA91249159FGFR3c.517C>T (p.Arg173Cys)
c.505C>T (p.Arg169Cys)
n.773C>T
n.792C>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.1801439G>ACA355975010FGFR3c.518G>A (p.Arg173His)
c.506G>A (p.Arg169His)
n.774G>A
n.793G>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.1801439G>CCA355975012FGFR3c.518G>C (p.Arg173Pro)
c.506G>C (p.Arg169Pro)
n.774G>C
n.793G>C
 dbSNP
4g.1801439G=CA1433504818FGFR3c.518G= (p.Arg173=)
c.506G= (p.Arg169=)
n.774G=
n.793G=
4g.1801439G>TCA355975014FGFR3c.518G>T (p.Arg173Leu)
c.506G>T (p.Arg169Leu)
n.774G>T
n.793G>T
 gnomAD v4
4g.1801440C>ACA438062777FGFR3c.519C>A (p.Arg173=)
c.507C>A (p.Arg169=)
n.775C>A
n.794C>A
4g.1801440C>GCA438062778FGFR3c.519C>G (p.Arg173=)
c.507C>G (p.Arg169=)
n.775C>G
n.794C>G
4g.1801440C>TCA438062779FGFR3c.519C>T (p.Arg173=)
c.507C>T (p.Arg169=)
n.775C>T
n.794C>T
 gnomAD v4
4g.1801441T>ACA355975016FGFR3c.520T>A (p.Phe174Ile)
c.508T>A (p.Phe170Ile)
n.776T>A
n.795T>A
4g.1801441T>CCA355975017FGFR3c.520T>C (p.Phe174Leu)
c.508T>C (p.Phe170Leu)
n.776T>C
n.795T>C
4g.1801441T>GCA355975019FGFR3c.520T>G (p.Phe174Val)
c.508T>G (p.Phe170Val)
n.776T>G
n.795T>G
4g.1801442T>ACA355975023FGFR3c.521T>A (p.Phe174Tyr)
c.509T>A (p.Phe170Tyr)
n.777T>A
n.796T>A
4g.1801442T>CCA355975025FGFR3c.521T>C (p.Phe174Ser)
c.509T>C (p.Phe170Ser)
n.777T>C
n.796T>C
4g.1801442T>GCA355975021FGFR3c.521T>G (p.Phe174Cys)
c.509T>G (p.Phe170Cys)
n.777T>G
n.796T>G
4g.1801443C>ACA355975026FGFR3c.522C>A (p.Phe174Leu)
c.510C>A (p.Phe170Leu)
n.778C>A
n.797C>A
 gnomAD v4
4g.1801443C>GCA355975028FGFR3c.522C>G (p.Phe174Leu)
c.510C>G (p.Phe170Leu)
n.778C>G
n.797C>G
4g.1801443C>TCA438062780FGFR3c.522C>T (p.Phe174=)
c.510C>T (p.Phe170=)
n.778C>T
n.797C>T
 gnomAD v4
4g.1801444C>ACA355975030FGFR3c.523C>A (p.Arg175Ser)
c.511C>A (p.Arg171Ser)
n.779C>A
n.798C>A
 gnomAD v4
4g.1801444C=CA1433504819FGFR3c.523C= (p.Arg175=)
c.511C= (p.Arg171=)
n.779C=
n.798C=
4g.1801444C>GCA355975031FGFR3c.523C>G (p.Arg175Gly)
c.511C>G (p.Arg171Gly)
n.779C>G
n.798C>G
4g.1801444C>TCA355975032FGFR3c.523C>T (p.Arg175Cys)
c.511C>T (p.Arg171Cys)
n.779C>T
n.798C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.1801445G>ACA2809863FGFR3c.524G>A (p.Arg175His)
c.512G>A (p.Arg171His)
n.780G>A
n.799G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.1801445G>CCA355975035FGFR3c.524G>C (p.Arg175Pro)
c.512G>C (p.Arg171Pro)
n.780G>C
n.799G>C
 dbSNP
4g.1801445G=CA1433504820FGFR3c.524G= (p.Arg175=)
c.512G= (p.Arg171=)
n.780G=
n.799G=
4g.1801445G>TCA355975036FGFR3c.524G>T (p.Arg175Leu)
c.512G>T (p.Arg171Leu)
n.780G>T
n.799G>T
 gnomAD v4
4g.1801446C>ACA438062781FGFR3c.525C>A (p.Arg175=)
c.513C>A (p.Arg171=)
n.781C>A
n.800C>A
 dbSNP gnomAD v3 gnomAD v4
4g.1801446C=CA1433504821FGFR3c.525C= (p.Arg175=)
c.513C= (p.Arg171=)
n.781C=
n.800C=
4g.1801446C>GCA438062782FGFR3c.525C>G (p.Arg175=)
c.513C>G (p.Arg171=)
n.781C>G
n.800C>G
4g.1801446C>TCA438062783FGFR3c.525C>T (p.Arg175=)
c.513C>T (p.Arg171=)
n.781C>T
n.800C>T
 gnomAD v4
4g.1801447T>ACA355975037FGFR3c.526T>A (p.Cys176Ser)
c.514T>A (p.Cys172Ser)
n.782T>A
n.801T>A
4g.1801447T>CCA355975038FGFR3c.526T>C (p.Cys176Arg)
c.514T>C (p.Cys172Arg)
n.782T>C
n.801T>C
 gnomAD v4
4g.1801447T>GCA355975040FGFR3c.526T>G (p.Cys176Gly)
c.514T>G (p.Cys172Gly)
n.782T>G
n.801T>G
4g.1801448G>ACA355975043FGFR3c.527G>A (p.Cys176Tyr)
c.515G>A (p.Cys172Tyr)
n.783G>A
n.802G>A
 dbSNP gnomAD v4
4g.1801448G>CCA355975045FGFR3c.527G>C (p.Cys176Ser)
c.515G>C (p.Cys172Ser)
n.783G>C
n.802G>C
 gnomAD v4
4g.1801448G>TCA355975042FGFR3c.527G>T (p.Cys176Phe)
c.515G>T (p.Cys172Phe)
n.783G>T
n.802G>T
 gnomAD v4
4g.1801449C>ACA355975047FGFR3c.528C>A (p.Cys176Ter)
c.516C>A (p.Cys172Ter)
n.784C>A
n.803C>A
 gnomAD v4
4g.1801449C=CA1433504822FGFR3c.528C= (p.Cys176=)
c.516C= (p.Cys172=)
n.784C=
n.803C=
4g.1801449C>GCA355975049FGFR3c.528C>G (p.Cys176Trp)
c.516C>G (p.Cys172Trp)
n.784C>G
n.803C>G
4g.1801449C>TCA438062784FGFR3c.528C>T (p.Cys176=)
c.516C>T (p.Cys172=)
n.784C>T
n.803C>T
 dbSNP gnomAD v2 gnomAD v4
4g.1801450C>ACA355975051FGFR3c.529C>A (p.Pro177Thr)
c.517C>A (p.Pro173Thr)
n.785C>A
n.804C>A
 gnomAD v4
4g.1801450C>GCA355975053FGFR3c.529C>G (p.Pro177Ala)
c.517C>G (p.Pro173Ala)
n.785C>G
n.804C>G
4g.1801450C>TCA355975055FGFR3c.529C>T (p.Pro177Ser)
c.517C>T (p.Pro173Ser)
n.785C>T
n.804C>T
4g.1801451C>ACA355975060FGFR3c.530C>A (p.Pro177Gln)
c.518C>A (p.Pro173Gln)
n.786C>A
n.805C>A
 dbSNP gnomAD v4
4g.1801451C>GCA355975056FGFR3c.530C>G (p.Pro177Arg)
c.518C>G (p.Pro173Arg)
n.786C>G
n.805C>G
4g.1801451C>TCA355975058FGFR3c.530C>T (p.Pro177Leu)
c.518C>T (p.Pro173Leu)
n.786C>T
n.805C>T
 gnomAD v4 COSMIC COSMIC
4g.1801451_1801452insCTGGCCA2669560528FGFR3c.530_531insCTGGC (p.Ala178TrpfsTer14)
c.518_519insCTGGC (p.Ala174TrpfsTer14)
n.786_787insCTGGC
n.805_806insCTGGC
 gnomAD v4
4g.1801452A=CA1433504823FGFR3c.531A= (p.Pro177=)
c.519A= (p.Pro173=)
n.787A=
n.806A=
4g.1801452A>CCA438062785FGFR3c.531A>C (p.Pro177=)
c.519A>C (p.Pro173=)
n.787A>C
n.806A>C
4g.1801452A>GCA438062786FGFR3c.531A>G (p.Pro177=)
c.519A>G (p.Pro173=)
n.787A>G
n.806A>G
 dbSNP gnomAD v4
4g.1801452A>TCA438062787FGFR3c.531A>T (p.Pro177=)
c.519A>T (p.Pro173=)
n.787A>T
n.806A>T
4g.1801453G>ACA355975062FGFR3c.532G>A (p.Ala178Thr)
c.520G>A (p.Ala174Thr)
n.788G>A
n.807G>A
 dbSNP gnomAD v4
4g.1801453G>CCA355975063FGFR3c.532G>C (p.Ala178Pro)
c.520G>C (p.Ala174Pro)
n.788G>C
n.807G>C
 dbSNP
4g.1801453G>TCA355975065FGFR3c.532G>T (p.Ala178Ser)
c.520G>T (p.Ala174Ser)
n.788G>T
n.807G>T
 dbSNP gnomAD v4
4g.1801455_1801456insTGCCTGCCCA2669560529FGFR3c.534_535insTGCCTGCC (p.Ala179CysfsTer14)
c.522_523insTGCCTGCC (p.Ala175CysfsTer14)
n.790_791insTGCCTGCC
n.809_810insTGCCTGCC
 gnomAD v4
4g.1801454C>ACA355975067FGFR3c.533C>A (p.Ala178Asp)
c.521C>A (p.Ala174Asp)
n.789C>A
n.808C>A
4g.1801454C>GCA355975069FGFR3c.533C>G (p.Ala178Gly)
c.521C>G (p.Ala174Gly)
n.789C>G
n.808C>G
4g.1801454C>TCA355975071FGFR3c.533C>T (p.Ala178Val)
c.521C>T (p.Ala174Val)
n.789C>T
n.808C>T
 dbSNP gnomAD v4
4g.1801455C>ACA438062788FGFR3c.534C>A (p.Ala178=)
c.522C>A (p.Ala174=)
n.790C>A
n.809C>A
4g.1801455C=CA1433504824FGFR3c.534C= (p.Ala178=)
c.522C= (p.Ala174=)
n.790C=
n.809C=
4g.1801455C>GCA438062789FGFR3c.534C>G (p.Ala178=)
c.522C>G (p.Ala174=)
n.790C>G
n.809C>G
4g.1801455C>TCA2809864FGFR3c.534C>T (p.Ala178=)
c.522C>T (p.Ala174=)
n.790C>T
n.809C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.1801456G>ACA2809865FGFR3c.535G>A (p.Ala179Thr)
c.523G>A (p.Ala175Thr)
n.791G>A
n.810G>A
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.1801456G>CCA355975073FGFR3c.535G>C (p.Ala179Pro)
c.523G>C (p.Ala175Pro)
n.791G>C
n.810G>C
 dbSNP
4g.1801456G=CA1433504825FGFR3c.535G= (p.Ala179=)
c.523G= (p.Ala175=)
n.791G=
n.810G=
4g.1801456G>TCA355975076FGFR3c.535G>T (p.Ala179Ser)
c.523G>T (p.Ala175Ser)
n.791G>T
n.810G>T
 gnomAD v4
4g.1801457C>ACA355975077FGFR3c.536C>A (p.Ala179Asp)
c.524C>A (p.Ala175Asp)
n.792C>A
n.811C>A
 dbSNP gnomAD v2 gnomAD v4
4g.1801457C=CA1433504826FGFR3c.536C= (p.Ala179=)
c.524C= (p.Ala175=)
n.792C=
n.811C=
4g.1801457C>GCA355975078FGFR3c.536C>G (p.Ala179Gly)
c.524C>G (p.Ala175Gly)
n.792C>G
n.811C>G
4g.1801457C>TCA355975081FGFR3c.536C>T (p.Ala179Val)
c.524C>T (p.Ala175Val)
n.792C>T
n.811C>T
 dbSNP gnomAD v2
4g.1801458T>ACA438062790FGFR3c.537T>A (p.Ala179=)
c.525T>A (p.Ala175=)
n.793T>A
n.812T>A
4g.1801458T>CCA438062791FGFR3c.537T>C (p.Ala179=)
c.525T>C (p.Ala175=)
n.793T>C
n.812T>C
4g.1801458T>GCA438062792FGFR3c.537T>G (p.Ala179=)
c.525T>G (p.Ala175=)
n.793T>G
n.812T>G
4g.1801459G>ACA355975083FGFR3c.538G>A (p.Gly180Ser)
c.526G>A (p.Gly176Ser)
n.794G>A
n.813G>A
 dbSNP
4g.1801459G>CCA355975085FGFR3c.538G>C (p.Gly180Arg)
c.526G>C (p.Gly176Arg)
n.794G>C
n.813G>C
4g.1801459G>TCA355975086FGFR3c.538G>T (p.Gly180Cys)
c.526G>T (p.Gly176Cys)
n.794G>T
n.813G>T
4g.1801460G>ACA355975088FGFR3c.539G>A (p.Gly180Asp)
c.527G>A (p.Gly176Asp)
n.795G>A
n.814G>A
 gnomAD v4 COSMIC COSMIC
4g.1801460G>CCA355975090FGFR3c.539G>C (p.Gly180Ala)
c.527G>C (p.Gly176Ala)
n.795G>C
n.814G>C
 dbSNP
4g.1801460G>TCA355975091FGFR3c.539G>T (p.Gly180Val)
c.527G>T (p.Gly176Val)
n.795G>T
n.814G>T
 gnomAD v4
4g.1801461C>ACA438062793FGFR3c.540C>A (p.Gly180=)
c.528C>A (p.Gly176=)
n.796C>A
n.815C>A
 gnomAD v4
4g.1801461C=CA1433504827FGFR3c.540C= (p.Gly180=)
c.528C= (p.Gly176=)
n.796C=
n.815C=
4g.1801461C>GCA438062794FGFR3c.540C>G (p.Gly180=)
c.528C>G (p.Gly176=)
n.796C>G
n.815C>G
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.1801461C>TCA438062795FGFR3c.540C>T (p.Gly180=)
c.528C>T (p.Gly176=)
n.796C>T
n.815C>T
 dbSNP gnomAD v4
4g.1801462A>CCA355975093FGFR3c.541A>C (p.Asn181His)
c.529A>C (p.Asn177His)
c.1A>C (p.Asn1His)
n.797A>C
n.816A>C
4g.1801462A>GCA355975094FGFR3c.541A>G (p.Asn181Asp)
c.529A>G (p.Asn177Asp)
c.1A>G (p.Asn1Asp)
n.797A>G
n.816A>G
4g.1801462A>TCA355975095FGFR3c.541A>T (p.Asn181Tyr)
c.529A>T (p.Asn177Tyr)
c.1A>T (p.Asn1Tyr)
n.797A>T
n.816A>T
4g.1801463A=CA1433504828FGFR3c.542A= (p.Asn181=)
c.530A= (p.Asn177=)
c.2A= (p.Asn1=)
n.798A=
n.817A=
4g.1801463A>CCA355975101FGFR3c.542A>C (p.Asn181Thr)
c.530A>C (p.Asn177Thr)
c.2A>C (p.Asn1Thr)
n.798A>C
n.817A>C
 dbSNP
4g.1801463A>GCA355975098FGFR3c.542A>G (p.Asn181Ser)
c.530A>G (p.Asn177Ser)
c.2A>G (p.Asn1Ser)
n.798A>G
n.817A>G
4g.1801463A>TCA355975099FGFR3c.542A>T (p.Asn181Ile)
c.530A>T (p.Asn177Ile)
c.2A>T (p.Asn1Ile)
n.798A>T
n.817A>T
 dbSNP gnomAD v2 gnomAD v4
4g.1801464C>ACA355975103FGFR3c.543C>A (p.Asn181Lys)
c.531C>A (p.Asn177Lys)
c.3C>A (p.Asn1Lys)
n.799C>A
n.818C>A
 gnomAD v4
4g.1801464C=CA1433504829FGFR3c.543C= (p.Asn181=)
c.531C= (p.Asn177=)
c.3C= (p.Asn1=)
n.799C=
n.818C=
4g.1801464C>GCA355975104FGFR3c.543C>G (p.Asn181Lys)
c.531C>G (p.Asn177Lys)
c.3C>G (p.Asn1Lys)
n.799C>G
n.818C>G
4g.1801464C>TCA438062796FGFR3c.543C>T (p.Asn181=)
c.531C>T (p.Asn177=)
c.3C>T (p.Asn1=)
n.799C>T
n.818C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.1801466_1801467delCA2760148334FGFR3c.545_546del (p.Pro182HisfsTer?)
c.533_534del (p.Pro178HisfsTer?)
c.5_6del (p.Pro2HisfsTer?)
n.801_802del
n.820_821del
4g.1801465C>ACA355975105FGFR3c.544C>A (p.Pro182Thr)
c.532C>A (p.Pro178Thr)
c.4C>A (p.Pro2Thr)
n.800C>A
n.819C>A
4g.1801465C>GCA355975107FGFR3c.544C>G (p.Pro182Ala)
c.532C>G (p.Pro178Ala)
c.4C>G (p.Pro2Ala)
n.800C>G
n.819C>G
4g.1801465C>TCA355975109FGFR3c.544C>T (p.Pro182Ser)
c.532C>T (p.Pro178Ser)
c.4C>T (p.Pro2Ser)
n.800C>T
n.819C>T
4g.1801466C>ACA355975110FGFR3c.545C>A (p.Pro182His)
c.533C>A (p.Pro178His)
c.5C>A (p.Pro2His)
n.801C>A
n.820C>A
 dbSNP gnomAD v4
4g.1801466C>GCA355975112FGFR3c.545C>G (p.Pro182Arg)
c.533C>G (p.Pro178Arg)
c.5C>G (p.Pro2Arg)
n.801C>G
n.820C>G
 dbSNP
4g.1801466C>TCA355975113FGFR3c.545C>T (p.Pro182Leu)
c.533C>T (p.Pro178Leu)
c.5C>T (p.Pro2Leu)
n.801C>T
n.820C>T
 gnomAD v4
4g.1801467C>ACA438062797FGFR3c.546C>A (p.Pro182=)
c.534C>A (p.Pro178=)
c.6C>A (p.Pro2=)
n.802C>A
n.821C>A
 gnomAD v4
4g.1801467C=CA1433504830FGFR3c.546C= (p.Pro182=)
c.534C= (p.Pro178=)
c.6C= (p.Pro2=)
n.802C=
n.821C=
4g.1801467C>GCA438062798FGFR3c.546C>G (p.Pro182=)
c.534C>G (p.Pro178=)
c.6C>G (p.Pro2=)
n.802C>G
n.821C>G
4g.1801467C>TCA91249172FGFR3c.546C>T (p.Pro182=)
c.534C>T (p.Pro178=)
c.6C>T (p.Pro2=)
n.802C>T
n.821C>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.1801468A>CCA355975114FGFR3c.547A>C (p.Thr183Pro)
c.535A>C (p.Thr179Pro)
c.7A>C (p.Thr3Pro)
n.803A>C
n.822A>C
4g.1801468A>GCA355975115FGFR3c.547A>G (p.Thr183Ala)
c.535A>G (p.Thr179Ala)
c.7A>G (p.Thr3Ala)
n.803A>G
n.822A>G
4g.1801468A>TCA355975117FGFR3c.547A>T (p.Thr183Ser)
c.535A>T (p.Thr179Ser)
c.7A>T (p.Thr3Ser)
n.803A>T
n.822A>T
4g.1801469C>ACA355975121FGFR3c.548C>A (p.Thr183Asn)
c.536C>A (p.Thr179Asn)
c.8C>A (p.Thr3Asn)
n.804C>A
n.823C>A
 gnomAD v4
4g.1801469C>GCA355975120FGFR3c.548C>G (p.Thr183Ser)
c.536C>G (p.Thr179Ser)
c.8C>G (p.Thr3Ser)
n.804C>G
n.823C>G
4g.1801469C>TCA355975119FGFR3c.548C>T (p.Thr183Ile)
c.536C>T (p.Thr179Ile)
c.8C>T (p.Thr3Ile)
n.804C>T
n.823C>T
4g.1801470T>ACA438062800FGFR3c.549T>A (p.Thr183=)
c.537T>A (p.Thr179=)
c.9T>A (p.Thr3=)
n.805T>A
n.824T>A
 gnomAD v4
4g.1801470T>CCA438062801FGFR3c.549T>C (p.Thr183=)
c.537T>C (p.Thr179=)
c.9T>C (p.Thr3=)
n.805T>C
n.824T>C
 gnomAD v4
4g.1801470T>GCA438062799FGFR3c.549T>G (p.Thr183=)
c.537T>G (p.Thr179=)
c.9T>G (p.Thr3=)
n.805T>G
n.824T>G
4g.1801471C>ACA355975122FGFR3c.550C>A (p.Pro184Thr)
c.538C>A (p.Pro180Thr)
c.10C>A (p.Pro4Thr)
n.806C>A
n.825C>A
 gnomAD v4
4g.1801471C>GCA355975123FGFR3c.550C>G (p.Pro184Ala)
c.538C>G (p.Pro180Ala)
c.10C>G (p.Pro4Ala)
n.806C>G
n.825C>G
4g.1801471C>TCA355975126FGFR3c.550C>T (p.Pro184Ser)
c.538C>T (p.Pro180Ser)
c.10C>T (p.Pro4Ser)
n.806C>T
n.825C>T
4g.1801472C>ACA355975128FGFR3c.551C>A (p.Pro184His)
c.539C>A (p.Pro180His)
c.11C>A (p.Pro4His)
n.807C>A
n.826C>A
 gnomAD v4
4g.1801472C>GCA355975129FGFR3c.551C>G (p.Pro184Arg)
c.539C>G (p.Pro180Arg)
c.11C>G (p.Pro4Arg)
n.807C>G
n.826C>G
4g.1801472C>TCA355975132FGFR3c.551C>T (p.Pro184Leu)
c.539C>T (p.Pro180Leu)
c.11C>T (p.Pro4Leu)
n.807C>T
n.826C>T
 gnomAD v4
4g.1801473C>ACA438062802FGFR3c.552C>A (p.Pro184=)
c.540C>A (p.Pro180=)
c.12C>A (p.Pro4=)
n.808C>A
n.827C>A
 dbSNP gnomAD v4
4g.1801473C=CA1433504831FGFR3c.552C= (p.Pro184=)
c.540C= (p.Pro180=)
c.12C= (p.Pro4=)
n.808C=
n.827C=
4g.1801473C>GCA438062803FGFR3c.552C>G (p.Pro184=)
c.540C>G (p.Pro180=)
c.12C>G (p.Pro4=)
n.808C>G
n.827C>G
4g.1801473C>TCA2809866FGFR3c.552C>T (p.Pro184=)
c.540C>T (p.Pro180=)
c.12C>T (p.Pro4=)
n.808C>T
n.827C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.1801474T>ACA355975136FGFR3c.553T>A (p.Ser185Thr)
c.541T>A (p.Ser181Thr)
c.13T>A (p.Ser5Thr)
n.809T>A
n.828T>A
 gnomAD v4
4g.1801474T>CCA355975139FGFR3c.553T>C (p.Ser185Pro)
c.541T>C (p.Ser181Pro)
c.13T>C (p.Ser5Pro)
n.809T>C
n.828T>C
4g.1801474T>GCA355975137FGFR3c.553T>G (p.Ser185Ala)
c.541T>G (p.Ser181Ala)
c.13T>G (p.Ser5Ala)
n.809T>G
n.828T>G
4g.1801475C>ACA355975141FGFR3c.554C>A (p.Ser185Tyr)
c.542C>A (p.Ser181Tyr)
c.14C>A (p.Ser5Tyr)
n.810C>A
n.829C>A
 gnomAD v4
4g.1801475C>GCA355975142FGFR3c.554C>G (p.Ser185Cys)
c.542C>G (p.Ser181Cys)
c.14C>G (p.Ser5Cys)
n.810C>G
n.829C>G
4g.1801475C>TCA355975144FGFR3c.554C>T (p.Ser185Phe)
c.542C>T (p.Ser181Phe)
c.14C>T (p.Ser5Phe)
n.810C>T
n.829C>T
 gnomAD v4
4g.1801476C>ACA2809867FGFR3c.555C>A (p.Ser185=)
c.543C>A (p.Ser181=)
c.15C>A (p.Ser5=)
n.811C>A
n.830C>A
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.1801476C=CA1433504832FGFR3c.555C= (p.Ser185=)
c.543C= (p.Ser181=)
c.15C= (p.Ser5=)
n.811C=
n.830C=
4g.1801476C>GCA438062804FGFR3c.555C>G (p.Ser185=)
c.543C>G (p.Ser181=)
c.15C>G (p.Ser5=)
n.811C>G
n.830C>G
4g.1801476C>TCA438062805FGFR3c.555C>T (p.Ser185=)
c.543C>T (p.Ser181=)
c.15C>T (p.Ser5=)
n.811C>T
n.830C>T
 gnomAD v4
4g.1801477A=CA1433504833FGFR3c.556A= (p.Ile186=)
c.544A= (p.Ile182=)
c.16A= (p.Ile6=)
n.812A=
n.831A=
4g.1801477A>CCA355975147FGFR3c.556A>C (p.Ile186Leu)
c.544A>C (p.Ile182Leu)
c.16A>C (p.Ile6Leu)
n.812A>C
n.831A>C
4g.1801477A>GCA355975150FGFR3c.556A>G (p.Ile186Val)
c.544A>G (p.Ile182Val)
c.16A>G (p.Ile6Val)
n.812A>G
n.831A>G
 ClinVar dbSNP gnomAD v4
4g.1801477A>TCA355975148FGFR3c.556A>T (p.Ile186Phe)
c.544A>T (p.Ile182Phe)
c.16A>T (p.Ile6Phe)
n.812A>T
n.831A>T
4g.1801478T>ACA355975152FGFR3c.557T>A (p.Ile186Asn)
c.545T>A (p.Ile182Asn)
c.17T>A (p.Ile6Asn)
n.813T>A
n.832T>A
 gnomAD v4
4g.1801478T>CCA355975153FGFR3c.557T>C (p.Ile186Thr)
c.545T>C (p.Ile182Thr)
c.17T>C (p.Ile6Thr)
n.813T>C
n.832T>C
4g.1801478T>GCA355975155FGFR3c.557T>G (p.Ile186Ser)
c.545T>G (p.Ile182Ser)
c.17T>G (p.Ile6Ser)
n.813T>G
n.832T>G
4g.1801479C>ACA438062807FGFR3c.558C>A (p.Ile186=)
c.546C>A (p.Ile182=)
c.18C>A (p.Ile6=)
n.814C>A
n.833C>A
 gnomAD v4
4g.1801479C=CA1433504834FGFR3c.558C= (p.Ile186=)
c.546C= (p.Ile182=)
c.18C= (p.Ile6=)
n.814C=
n.833C=
4g.1801479C>GCA355975160FGFR3c.558C>G (p.Ile186Met)
c.546C>G (p.Ile182Met)
c.18C>G (p.Ile6Met)
n.814C>G
n.833C>G
4g.1801479C>TCA438062806FGFR3c.558C>T (p.Ile186=)
c.546C>T (p.Ile182=)
c.18C>T (p.Ile6=)
n.814C>T
n.833C>T
 dbSNP gnomAD v2
4g.1801480T>ACA355975162FGFR3c.559T>A (p.Ser187Thr)
c.547T>A (p.Ser183Thr)
c.19T>A (p.Ser7Thr)
n.815T>A
n.834T>A
4g.1801480T>CCA355975163FGFR3c.559T>C (p.Ser187Pro)
c.547T>C (p.Ser183Pro)
c.19T>C (p.Ser7Pro)
n.815T>C
n.834T>C
4g.1801480T>GCA355975165FGFR3c.559T>G (p.Ser187Ala)
c.547T>G (p.Ser183Ala)
c.19T>G (p.Ser7Ala)
n.815T>G
n.834T>G
4g.1801481C>ACA2809868FGFR3c.560C>A (p.Ser187Tyr)
c.548C>A (p.Ser183Tyr)
c.20C>A (p.Ser7Tyr)
n.816C>A
n.835C>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.1801481C=CA1433504835FGFR3c.560C= (p.Ser187=)
c.548C= (p.Ser183=)
c.20C= (p.Ser7=)
n.816C=
n.835C=
4g.1801481C>GCA355975167FGFR3c.560C>G (p.Ser187Cys)
c.548C>G (p.Ser183Cys)
c.20C>G (p.Ser7Cys)
n.816C>G
n.835C>G
4g.1801481C>TCA355975169FGFR3c.560C>T (p.Ser187Phe)
c.548C>T (p.Ser183Phe)
c.20C>T (p.Ser7Phe)
n.816C>T
n.835C>T
 gnomAD v4
4g.1801482C>ACA438062808FGFR3c.561C>A (p.Ser187=)
c.549C>A (p.Ser183=)
c.21C>A (p.Ser7=)
n.817C>A
n.836C>A
 gnomAD v4
4g.1801482C=CA1433504836FGFR3c.561C= (p.Ser187=)
c.549C= (p.Ser183=)
c.21C= (p.Ser7=)
n.817C=
n.836C=
4g.1801482C>GCA438062810FGFR3c.561C>G (p.Ser187=)
c.549C>G (p.Ser183=)
c.21C>G (p.Ser7=)
n.817C>G
n.836C>G
 dbSNP
4g.1801482C>TCA438062809FGFR3c.561C>T (p.Ser187=)
c.549C>T (p.Ser183=)
c.21C>T (p.Ser7=)
n.817C>T
n.836C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.1801483T>ACA355975174FGFR3c.562T>A (p.Trp188Arg)
c.550T>A (p.Trp184Arg)
c.22T>A (p.Trp8Arg)
n.818T>A
n.837T>A
4g.1801483T>CCA355975173FGFR3c.562T>C (p.Trp188Arg)
c.550T>C (p.Trp184Arg)
c.22T>C (p.Trp8Arg)
n.818T>C
n.837T>C
 gnomAD v4
4g.1801483T>GCA355975171FGFR3c.562T>G (p.Trp188Gly)
c.550T>G (p.Trp184Gly)
c.22T>G (p.Trp8Gly)
n.818T>G
n.837T>G
4g.1801484G>ACA355975176FGFR3c.563G>A (p.Trp188Ter)
c.551G>A (p.Trp184Ter)
c.23G>A (p.Trp8Ter)
n.819G>A
n.838G>A
4g.1801484G>CCA355975180FGFR3c.563G>C (p.Trp188Ser)
c.551G>C (p.Trp184Ser)
c.23G>C (p.Trp8Ser)
n.819G>C
n.838G>C
 dbSNP
4g.1801484G>TCA355975178FGFR3c.563G>T (p.Trp188Leu)
c.551G>T (p.Trp184Leu)
c.23G>T (p.Trp8Leu)
n.819G>T
n.838G>T
 gnomAD v4
4g.1801485G>ACA355975181FGFR3c.564G>A (p.Trp188Ter)
c.552G>A (p.Trp184Ter)
c.24G>A (p.Trp8Ter)
n.820G>A
n.839G>A
 dbSNP gnomAD v4
4g.1801485G>CCA355975182FGFR3c.564G>C (p.Trp188Cys)
c.552G>C (p.Trp184Cys)
c.24G>C (p.Trp8Cys)
n.820G>C
n.839G>C
4g.1801485G>TCA355975183FGFR3c.564G>T (p.Trp188Cys)
c.552G>T (p.Trp184Cys)
c.24G>T (p.Trp8Cys)
n.820G>T
n.839G>T
4g.1801486C>ACA355975184FGFR3c.565C>A (p.Leu189Met)
c.553C>A (p.Leu185Met)
c.25C>A (p.Leu9Met)
n.821C>A
n.840C>A
 gnomAD v4
4g.1801486C=CA1433504837FGFR3c.565C= (p.Leu189=)
c.553C= (p.Leu185=)
c.25C= (p.Leu9=)
n.821C=
n.840C=
4g.1801486C>GCA355975185FGFR3c.565C>G (p.Leu189Val)
c.553C>G (p.Leu185Val)
c.25C>G (p.Leu9Val)
n.821C>G
n.840C>G
4g.1801486C>TCA91249178FGFR3c.565C>T (p.Leu189=)
c.553C>T (p.Leu185=)
c.25C>T (p.Leu9=)
n.821C>T
n.840C>T
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.1801487T>ACA355975188FGFR3c.566T>A (p.Leu189Gln)
c.554T>A (p.Leu185Gln)
c.26T>A (p.Leu9Gln)
n.822T>A
n.841T>A
4g.1801487T>CCA355975189FGFR3c.566T>C (p.Leu189Pro)
c.554T>C (p.Leu185Pro)
c.26T>C (p.Leu9Pro)
n.822T>C
n.841T>C
4g.1801487T>GCA355975191FGFR3c.566T>G (p.Leu189Arg)
c.554T>G (p.Leu185Arg)
c.26T>G (p.Leu9Arg)
n.822T>G
n.841T>G
 dbSNP
4g.1801487T=CA1433504838FGFR3c.566T= (p.Leu189=)
c.554T= (p.Leu185=)
c.26T= (p.Leu9=)
n.822T=
n.841T=
4g.1801488G>ACA438062811FGFR3c.567G>A (p.Leu189=)
c.555G>A (p.Leu185=)
c.27G>A (p.Leu9=)
n.823G>A
n.842G>A
 gnomAD v4
4g.1801488G>CCA438062812FGFR3c.567G>C (p.Leu189=)
c.555G>C (p.Leu185=)
c.27G>C (p.Leu9=)
n.823G>C
n.842G>C
 gnomAD v4
4g.1801488G>TCA438062813FGFR3c.567G>T (p.Leu189=)
c.555G>T (p.Leu185=)
c.27G>T (p.Leu9=)
n.823G>T
n.842G>T
 gnomAD v4
4g.1801489A=CA1433504839FGFR3c.568A= (p.Lys190=)
c.556A= (p.Lys186=)
c.28A= (p.Lys10=)
n.824A=
n.843A=
4g.1801489A>CCA355975193FGFR3c.568A>C (p.Lys190Gln)
c.556A>C (p.Lys186Gln)
c.28A>C (p.Lys10Gln)
n.824A>C
n.843A>C
 dbSNP gnomAD v2 gnomAD v4
4g.1801489A>GCA355975195FGFR3c.568A>G (p.Lys190Glu)
c.556A>G (p.Lys186Glu)
c.28A>G (p.Lys10Glu)
n.824A>G
n.843A>G
4g.1801489A>TCA355975196FGFR3c.568A>T (p.Lys190Ter)
c.556A>T (p.Lys186Ter)
c.28A>T (p.Lys10Ter)
n.824A>T
n.843A>T
4g.1801490A>CCA355975198FGFR3c.569A>C (p.Lys190Thr)
c.557A>C (p.Lys186Thr)
c.29A>C (p.Lys10Thr)
n.825A>C
n.844A>C
4g.1801490A>GCA355975200FGFR3c.569A>G (p.Lys190Arg)
c.557A>G (p.Lys186Arg)
c.29A>G (p.Lys10Arg)
n.825A>G
n.844A>G
 gnomAD v4
4g.1801490A>TCA355975202FGFR3c.569A>T (p.Lys190Met)
c.557A>T (p.Lys186Met)
c.29A>T (p.Lys10Met)
n.825A>T
n.844A>T
4g.1801491G>ACA438062814FGFR3c.570G>A (p.Lys190=)
c.558G>A (p.Lys186=)
c.30G>A (p.Lys10=)
n.826G>A
n.845G>A
 dbSNP gnomAD v2
4g.1801491G>CCA355975204FGFR3c.570G>C (p.Lys190Asn)
c.558G>C (p.Lys186Asn)
c.30G>C (p.Lys10Asn)
n.826G>C
n.845G>C
4g.1801491G=CA1433504840FGFR3c.570G= (p.Lys190=)
c.558G= (p.Lys186=)
c.30G= (p.Lys10=)
n.826G=
n.845G=
4g.1801491G>TCA355975205FGFR3c.570G>T (p.Lys190Asn)
c.558G>T (p.Lys186Asn)
c.30G>T (p.Lys10Asn)
n.826G>T
n.845G>T
 gnomAD v4
4g.1801492A>CCA355975208FGFR3c.571A>C (p.Asn191His)
c.559A>C (p.Asn187His)
c.31A>C (p.Asn11His)
n.827A>C
n.846A>C
4g.1801492A>GCA355975209FGFR3c.571A>G (p.Asn191Asp)
c.559A>G (p.Asn187Asp)
c.31A>G (p.Asn11Asp)
n.827A>G
n.846A>G
 gnomAD v4
4g.1801492A>TCA355975211FGFR3c.571A>T (p.Asn191Tyr)
c.559A>T (p.Asn187Tyr)
c.31A>T (p.Asn11Tyr)
n.827A>T
n.846A>T
4g.1801493A>CCA355975214FGFR3c.572A>C (p.Asn191Thr)
c.560A>C (p.Asn187Thr)
c.32A>C (p.Asn11Thr)
n.828A>C
n.847A>C
 dbSNP
4g.1801493A>GCA355975216FGFR3c.572A>G (p.Asn191Ser)
c.560A>G (p.Asn187Ser)
c.32A>G (p.Asn11Ser)
n.828A>G
n.847A>G
4g.1801493A>TCA355975218FGFR3c.572A>T (p.Asn191Ile)
c.560A>T (p.Asn187Ile)
c.32A>T (p.Asn11Ile)
n.828A>T
n.847A>T
4g.1801494C>ACA355975220FGFR3c.573C>A (p.Asn191Lys)
c.561C>A (p.Asn187Lys)
c.33C>A (p.Asn11Lys)
n.829C>A
n.848C>A
 gnomAD v4
4g.1801494C=CA1433504841FGFR3c.573C= (p.Asn191=)
c.561C= (p.Asn187=)
c.33C= (p.Asn11=)
n.829C=
n.848C=
4g.1801494C>GCA355975221FGFR3c.573C>G (p.Asn191Lys)
c.561C>G (p.Asn187Lys)
c.33C>G (p.Asn11Lys)
n.829C>G
n.848C>G
 dbSNP
4g.1801494C>TCA2809869FGFR3c.573C>T (p.Asn191=)
c.561C>T (p.Asn187=)
c.33C>T (p.Asn11=)
n.829C>T
n.848C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.1801495G>ACA355975223FGFR3c.574G>A (p.Gly192Ser)
c.562G>A (p.Gly188Ser)
c.34G>A (p.Gly12Ser)
n.830G>A
n.849G>A
 dbSNP gnomAD v4
4g.1801495G>CCA355975224FGFR3c.574G>C (p.Gly192Arg)
c.562G>C (p.Gly188Arg)
c.34G>C (p.Gly12Arg)
n.830G>C
n.849G>C
4g.1801495G>TCA355975226FGFR3c.574G>T (p.Gly192Cys)
c.562G>T (p.Gly188Cys)
c.34G>T (p.Gly12Cys)
n.830G>T
n.849G>T
 gnomAD v4
4g.1801496G>ACA355975227FGFR3c.575G>A (p.Gly192Asp)
c.563G>A (p.Gly188Asp)
c.35G>A (p.Gly12Asp)
n.831G>A
n.850G>A
 dbSNP gnomAD v2 gnomAD v4
4g.1801496G>CCA355975230FGFR3c.575G>C (p.Gly192Ala)
c.563G>C (p.Gly188Ala)
c.35G>C (p.Gly12Ala)
n.831G>C
n.850G>C
4g.1801496G=CA1433504842FGFR3c.575G= (p.Gly192=)
c.563G= (p.Gly188=)
c.35G= (p.Gly12=)
n.831G=
n.850G=
4g.1801496G>TCA355975229FGFR3c.575G>T (p.Gly192Val)
c.563G>T (p.Gly188Val)
c.35G>T (p.Gly12Val)
n.831G>T
n.850G>T
 gnomAD v4
4g.1801497C>ACA438062815FGFR3c.576C>A (p.Gly192=)
c.564C>A (p.Gly188=)
c.36C>A (p.Gly12=)
n.832C>A
n.851C>A
 dbSNP gnomAD v4
4g.1801497C=CA1433504843FGFR3c.576C= (p.Gly192=)
c.564C= (p.Gly188=)
c.36C= (p.Gly12=)
n.832C=
n.851C=
4g.1801497C>GCA438062816FGFR3c.576C>G (p.Gly192=)
c.564C>G (p.Gly188=)
c.36C>G (p.Gly12=)
n.832C>G
n.851C>G
 gnomAD v4
4g.1801497C>TCA438062817FGFR3c.576C>T (p.Gly192=)
c.564C>T (p.Gly188=)
c.36C>T (p.Gly12=)
n.832C>T
n.851C>T
 dbSNP COSMIC COSMIC
4g.1801498A=CA1433504844FGFR3c.577A= (p.Arg193=)
c.565A= (p.Arg189=)
c.37A= (p.Arg13=)
n.833A=
n.852A=
4g.1801498A>CCA438062818FGFR3c.577A>C (p.Arg193=)
c.565A>C (p.Arg189=)
c.37A>C (p.Arg13=)
n.833A>C
n.852A>C
4g.1801498A>GCA355975232FGFR3c.577A>G (p.Arg193Gly)
c.565A>G (p.Arg189Gly)
c.37A>G (p.Arg13Gly)
n.833A>G
n.852A>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
4g.1801498A>TCA355975234FGFR3c.577A>T (p.Arg193Trp)
c.565A>T (p.Arg189Trp)
c.37A>T (p.Arg13Trp)
n.833A>T
n.852A>T
4g.1801499G>ACA355975236FGFR3c.578G>A (p.Arg193Lys)
c.566G>A (p.Arg189Lys)
c.38G>A (p.Arg13Lys)
n.834G>A
n.853G>A
4g.1801499G>CCA355975237FGFR3c.578G>C (p.Arg193Thr)
c.566G>C (p.Arg189Thr)
c.38G>C (p.Arg13Thr)
n.834G>C
n.853G>C
4g.1801499G>TCA355975239FGFR3c.578G>T (p.Arg193Met)
c.566G>T (p.Arg189Met)
c.38G>T (p.Arg13Met)
n.834G>T
n.853G>T
 gnomAD v4
4g.1801500G>ACA438062819FGFR3c.579G>A (p.Arg193=)
c.567G>A (p.Arg189=)
c.39G>A (p.Arg13=)
n.835G>A
n.854G>A
4g.1801500G>CCA355975241FGFR3c.579G>C (p.Arg193Ser)
c.567G>C (p.Arg189Ser)
c.39G>C (p.Arg13Ser)
n.835G>C
n.854G>C
4g.1801500G>TCA355975242FGFR3c.579G>T (p.Arg193Ser)
c.567G>T (p.Arg189Ser)
c.39G>T (p.Arg13Ser)
n.835G>T
n.854G>T
 gnomAD v4
4g.1801501G>ACA355975245FGFR3c.580G>A (p.Glu194Lys)
c.568G>A (p.Glu190Lys)
c.40G>A (p.Glu14Lys)
n.836G>A
n.855G>A
 COSMIC COSMIC
4g.1801501G>CCA355975247FGFR3c.580G>C (p.Glu194Gln)
c.568G>C (p.Glu190Gln)
c.40G>C (p.Glu14Gln)
n.836G>C
n.855G>C
4g.1801501G>TCA355975248FGFR3c.580G>T (p.Glu194Ter)
c.568G>T (p.Glu190Ter)
c.40G>T (p.Glu14Ter)
n.836G>T
n.855G>T
4g.1801502A=CA1433504845FGFR3c.581A= (p.Glu194=)
c.569A= (p.Glu190=)
c.41A= (p.Glu14=)
n.837A=
n.856A=
4g.1801502A>CCA355975251FGFR3c.581A>C (p.Glu194Ala)
c.569A>C (p.Glu190Ala)
c.41A>C (p.Glu14Ala)
n.837A>C
n.856A>C
4g.1801502A>GCA355975252FGFR3c.581A>G (p.Glu194Gly)
c.569A>G (p.Glu190Gly)
c.41A>G (p.Glu14Gly)
n.837A>G
n.856A>G
 gnomAD v4
4g.1801502A>TCA2809870FGFR3c.581A>T (p.Glu194Val)
c.569A>T (p.Glu190Val)
c.41A>T (p.Glu14Val)
n.837A>T
n.856A>T
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.1801503G>ACA438062820FGFR3c.582G>A (p.Glu194=)
c.570G>A (p.Glu190=)
c.42G>A (p.Glu14=)
n.838G>A
n.857G>A
 dbSNP gnomAD v4
4g.1801503G>CCA355975255FGFR3c.582G>C (p.Glu194Asp)
c.570G>C (p.Glu190Asp)
c.42G>C (p.Glu14Asp)
n.838G>C
n.857G>C
4g.1801503G>TCA355975257FGFR3c.582G>T (p.Glu194Asp)
c.570G>T (p.Glu190Asp)
c.42G>T (p.Glu14Asp)
n.838G>T
n.857G>T
 gnomAD v4
4g.1801504T>ACA355975258FGFR3c.583T>A (p.Phe195Ile)
c.571T>A (p.Phe191Ile)
c.43T>A (p.Phe15Ile)
n.839T>A
n.858T>A
4g.1801504T>CCA355975260FGFR3c.583T>C (p.Phe195Leu)
c.571T>C (p.Phe191Leu)
c.43T>C (p.Phe15Leu)
n.839T>C
n.858T>C
 gnomAD v4
4g.1801504T>GCA355975262FGFR3c.583T>G (p.Phe195Val)
c.571T>G (p.Phe191Val)
c.43T>G (p.Phe15Val)
n.839T>G
n.858T>G
 dbSNP gnomAD v4
4g.1801505T>ACA355975264FGFR3c.584T>A (p.Phe195Tyr)
c.572T>A (p.Phe191Tyr)
c.44T>A (p.Phe15Tyr)
n.840T>A
n.859T>A
4g.1801505T>CCA355975265FGFR3c.584T>C (p.Phe195Ser)
c.572T>C (p.Phe191Ser)
c.44T>C (p.Phe15Ser)
n.840T>C
n.859T>C
4g.1801505T>GCA355975266FGFR3c.584T>G (p.Phe195Cys)
c.572T>G (p.Phe191Cys)
c.44T>G (p.Phe15Cys)
n.840T>G
n.859T>G
4g.1801506C>ACA355975268FGFR3c.585C>A (p.Phe195Leu)
c.573C>A (p.Phe191Leu)
c.45C>A (p.Phe15Leu)
n.841C>A
n.860C>A
 dbSNP gnomAD v4
4g.1801506C=CA1433504846FGFR3c.585C= (p.Phe195=)
c.573C= (p.Phe191=)
c.45C= (p.Phe15=)
n.841C=
n.860C=
4g.1801506C>GCA91249187FGFR3c.585C>G (p.Phe195Leu)
c.573C>G (p.Phe191Leu)
c.45C>G (p.Phe15Leu)
n.841C>G
n.860C>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.1801506C>TCA438062821FGFR3c.585C>T (p.Phe195=)
c.573C>T (p.Phe191=)
c.45C>T (p.Phe15=)
n.841C>T
n.860C>T
 gnomAD v4
4g.1801507C>ACA91249220FGFR3c.586C>A (p.Arg196Ser)
c.574C>A (p.Arg192Ser)
c.46C>A (p.Arg16Ser)
n.842C>A
n.861C>A
 dbSNP gnomAD v4
4g.1801507C=CA1433504847FGFR3c.586C= (p.Arg196=)
c.574C= (p.Arg192=)
c.46C= (p.Arg16=)
n.842C=
n.861C=
4g.1801507C>GCA355975273FGFR3c.586C>G (p.Arg196Gly)
c.574C>G (p.Arg192Gly)
c.46C>G (p.Arg16Gly)
n.842C>G
n.861C>G
4g.1801507C>TCA355975276FGFR3c.586C>T (p.Arg196Cys)
c.574C>T (p.Arg192Cys)
c.46C>T (p.Arg16Cys)
n.842C>T
n.861C>T
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
4g.1801508G>ACA91249225FGFR3c.587G>A (p.Arg196His)
c.575G>A (p.Arg192His)
c.47G>A (p.Arg16His)
n.843G>A
n.862G>A
 dbSNP gnomAD v2 gnomAD v4 COSMIC
4g.1801508G>CCA355975280FGFR3c.587G>C (p.Arg196Pro)
c.575G>C (p.Arg192Pro)
c.47G>C (p.Arg16Pro)
n.843G>C
n.862G>C
4g.1801508G=CA1433504848FGFR3c.587G= (p.Arg196=)
c.575G= (p.Arg192=)
c.47G= (p.Arg16=)
n.843G=
n.862G=
4g.1801508G>TCA355975278FGFR3c.587G>T (p.Arg196Leu)
c.575G>T (p.Arg192Leu)
c.47G>T (p.Arg16Leu)
n.843G>T
n.862G>T
 gnomAD v4
4g.1801509C>ACA438062822FGFR3c.588C>A (p.Arg196=)
c.576C>A (p.Arg192=)
c.48C>A (p.Arg16=)
n.844C>A
n.863C>A
 gnomAD v4
4g.1801509C=CA1433504849FGFR3c.588C= (p.Arg196=)
c.576C= (p.Arg192=)
c.48C= (p.Arg16=)
n.844C=
n.863C=
4g.1801509C>GCA438062823FGFR3c.588C>G (p.Arg196=)
c.576C>G (p.Arg192=)
c.48C>G (p.Arg16=)
n.844C>G
n.863C>G
 dbSNP
4g.1801509C>TCA202984FGFR3c.588C>T (p.Arg196=)
c.576C>T (p.Arg192=)
c.48C>T (p.Arg16=)
n.844C>T
n.863C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC

Number of alleles fetched