Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.1805879A>CCA355981897FGFR3c.1781A>C (p.Lys594Thr)
c.*831A>C (n.*831A>C)
c.1439A>C (p.Lys480Thr)
c.1763A>C (p.Lys588Thr)
c.1775A>C (p.Lys592Thr)
c.1778A>C (p.Lys593Thr)
c.1787A>C (p.Lys596Thr)
c.1784A>C (p.Lys595Thr)
n.2182A>C
n.2201A>C
4g.1805879A>GCA355981898FGFR3c.1781A>G (p.Lys594Arg)
c.*831A>G (n.*831A>G)
c.1439A>G (p.Lys480Arg)
c.1763A>G (p.Lys588Arg)
c.1775A>G (p.Lys592Arg)
c.1778A>G (p.Lys593Arg)
c.1787A>G (p.Lys596Arg)
c.1784A>G (p.Lys595Arg)
n.2182A>G
n.2201A>G
4g.1805879A>TCA355981899FGFR3c.1781A>T (p.Lys594Met)
c.*831A>T (n.*831A>T)
c.1439A>T (p.Lys480Met)
c.1763A>T (p.Lys588Met)
c.1775A>T (p.Lys592Met)
c.1778A>T (p.Lys593Met)
c.1787A>T (p.Lys596Met)
c.1784A>T (p.Lys595Met)
n.2182A>T
n.2201A>T
4g.1805880G>ACA2810577FGFR3c.1782G>A (p.Lys594=)
c.*832G>A (n.*832G>A)
c.1440G>A (p.Lys480=)
c.1764G>A (p.Lys588=)
c.1776G>A (p.Lys592=)
c.1779G>A (p.Lys593=)
c.1788G>A (p.Lys596=)
c.1785G>A (p.Lys595=)
n.2183G>A
n.2202G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.1805880G>CCA355981900FGFR3c.1782G>C (p.Lys594Asn)
c.*832G>C (n.*832G>C)
c.1440G>C (p.Lys480Asn)
c.1764G>C (p.Lys588Asn)
c.1776G>C (p.Lys592Asn)
c.1779G>C (p.Lys593Asn)
c.1788G>C (p.Lys596Asn)
c.1785G>C (p.Lys595Asn)
n.2183G>C
n.2202G>C
4g.1805880G=CA1433507668FGFR3c.1782G= (p.Lys594=)
c.*832G= (n.*832G=)
c.1440G= (p.Lys480=)
c.1764G= (p.Lys588=)
c.1776G= (p.Lys592=)
c.1779G= (p.Lys593=)
c.1788G= (p.Lys596=)
c.1785G= (p.Lys595=)
n.2183G=
n.2202G=
4g.1805880G>TCA355981901FGFR3c.1782G>T (p.Lys594Asn)
c.*832G>T (n.*832G>T)
c.1440G>T (p.Lys480Asn)
c.1764G>T (p.Lys588Asn)
c.1776G>T (p.Lys592Asn)
c.1779G>T (p.Lys593Asn)
c.1788G>T (p.Lys596Asn)
c.1785G>T (p.Lys595Asn)
n.2183G>T
n.2202G>T
4g.1805881G>ACA355981903FGFR3c.1783G>A (p.Asp595Asn)
c.*833G>A (n.*833G>A)
c.1441G>A (p.Asp481Asn)
c.1765G>A (p.Asp589Asn)
c.1777G>A (p.Asp593Asn)
c.1780G>A (p.Asp594Asn)
c.1789G>A (p.Asp597Asn)
c.1786G>A (p.Asp596Asn)
n.2184G>A
n.2203G>A
gnomAD v4
4g.1805881G>CCA91257303FGFR3c.1783G>C (p.Asp595His)
c.*833G>C (n.*833G>C)
c.1441G>C (p.Asp481His)
c.1765G>C (p.Asp589His)
c.1777G>C (p.Asp593His)
c.1780G>C (p.Asp594His)
c.1789G>C (p.Asp597His)
c.1786G>C (p.Asp596His)
n.2184G>C
n.2203G>C
dbSNP gnomAD v4
4g.1805881G=CA1433507669FGFR3c.1783G= (p.Asp595=)
c.*833G= (n.*833G=)
c.1441G= (p.Asp481=)
c.1765G= (p.Asp589=)
c.1777G= (p.Asp593=)
c.1780G= (p.Asp594=)
c.1789G= (p.Asp597=)
c.1786G= (p.Asp596=)
n.2184G=
n.2203G=
4g.1805881G>TCA355981902FGFR3c.1783G>T (p.Asp595Tyr)
c.*833G>T (n.*833G>T)
c.1441G>T (p.Asp481Tyr)
c.1765G>T (p.Asp589Tyr)
c.1777G>T (p.Asp593Tyr)
c.1780G>T (p.Asp594Tyr)
c.1789G>T (p.Asp597Tyr)
c.1786G>T (p.Asp596Tyr)
n.2184G>T
n.2203G>T
dbSNP gnomAD v2 gnomAD v4
4g.1805881_1805882delinsTGCA2697557053FGFR3c.1783_1784delinsTG (p.Asp595Cys)
c.*833_*834delinsTG (n.*833_*834delinsTG)
c.1441_1442delinsTG (p.Asp481Cys)
c.1765_1766delinsTG (p.Asp589Cys)
c.1777_1778delinsTG (p.Asp593Cys)
c.1780_1781delinsTG (p.Asp594Cys)
c.1789_1790delinsTG (p.Asp597Cys)
c.1786_1787delinsTG (p.Asp596Cys)
n.2184_2185delinsTG
n.2203_2204delinsTG
ClinVar
4g.1805882A>CCA355981904FGFR3c.1784A>C (p.Asp595Ala)
c.*834A>C (n.*834A>C)
c.1442A>C (p.Asp481Ala)
c.1766A>C (p.Asp589Ala)
c.1778A>C (p.Asp593Ala)
c.1781A>C (p.Asp594Ala)
c.1790A>C (p.Asp597Ala)
c.1787A>C (p.Asp596Ala)
n.2185A>C
n.2204A>C
4g.1805882A>GCA355981905FGFR3c.1784A>G (p.Asp595Gly)
c.*834A>G (n.*834A>G)
c.1442A>G (p.Asp481Gly)
c.1766A>G (p.Asp589Gly)
c.1778A>G (p.Asp593Gly)
c.1781A>G (p.Asp594Gly)
c.1790A>G (p.Asp597Gly)
c.1787A>G (p.Asp596Gly)
n.2185A>G
n.2204A>G
gnomAD v4
4g.1805882A>TCA355981906FGFR3c.1784A>T (p.Asp595Val)
c.*834A>T (n.*834A>T)
c.1442A>T (p.Asp481Val)
c.1766A>T (p.Asp589Val)
c.1778A>T (p.Asp593Val)
c.1781A>T (p.Asp594Val)
c.1790A>T (p.Asp597Val)
c.1787A>T (p.Asp596Val)
n.2185A>T
n.2204A>T
dbSNP
4g.1805883C>ACA355981907FGFR3c.1785C>A (p.Asp595Glu)
c.*835C>A (n.*835C>A)
c.1443C>A (p.Asp481Glu)
c.1767C>A (p.Asp589Glu)
c.1779C>A (p.Asp593Glu)
c.1782C>A (p.Asp594Glu)
c.1791C>A (p.Asp597Glu)
c.1788C>A (p.Asp596Glu)
n.2186C>A
n.2205C>A
4g.1805883C=CA1433507670FGFR3c.1785C= (p.Asp595=)
c.*835C= (n.*835C=)
c.1443C= (p.Asp481=)
c.1767C= (p.Asp589=)
c.1779C= (p.Asp593=)
c.1782C= (p.Asp594=)
c.1791C= (p.Asp597=)
c.1788C= (p.Asp596=)
n.2186C=
n.2205C=
4g.1805883C>GCA355981908FGFR3c.1785C>G (p.Asp595Glu)
c.*835C>G (n.*835C>G)
c.1443C>G (p.Asp481Glu)
c.1767C>G (p.Asp589Glu)
c.1779C>G (p.Asp593Glu)
c.1782C>G (p.Asp594Glu)
c.1791C>G (p.Asp597Glu)
c.1788C>G (p.Asp596Glu)
n.2186C>G
n.2205C>G
dbSNP gnomAD v4
4g.1805883C>TCA2810578FGFR3c.1785C>T (p.Asp595=)
c.*835C>T (n.*835C>T)
c.1443C>T (p.Asp481=)
c.1767C>T (p.Asp589=)
c.1779C>T (p.Asp593=)
c.1782C>T (p.Asp594=)
c.1791C>T (p.Asp597=)
c.1788C>T (p.Asp596=)
n.2186C>T
n.2205C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.1805884C>ACA355981909FGFR3c.1786C>A (p.Leu596Met)
c.*836C>A (n.*836C>A)
c.1444C>A (p.Leu482Met)
c.1768C>A (p.Leu590Met)
c.1780C>A (p.Leu594Met)
c.1783C>A (p.Leu595Met)
c.1792C>A (p.Leu598Met)
c.1789C>A (p.Leu597Met)
n.2187C>A
n.2206C>A
4g.1805884C=CA1433507671FGFR3c.1786C= (p.Leu596=)
c.*836C= (n.*836C=)
c.1444C= (p.Leu482=)
c.1768C= (p.Leu590=)
c.1780C= (p.Leu594=)
c.1783C= (p.Leu595=)
c.1792C= (p.Leu598=)
c.1789C= (p.Leu597=)
n.2187C=
n.2206C=
4g.1805884C>GCA355981910FGFR3c.1786C>G (p.Leu596Val)
c.*836C>G (n.*836C>G)
c.1444C>G (p.Leu482Val)
c.1768C>G (p.Leu590Val)
c.1780C>G (p.Leu594Val)
c.1783C>G (p.Leu595Val)
c.1792C>G (p.Leu598Val)
c.1789C>G (p.Leu597Val)
n.2187C>G
n.2206C>G
4g.1805884C>TCA2810579FGFR3c.1786C>T (p.Leu596=)
c.*836C>T (n.*836C>T)
c.1444C>T (p.Leu482=)
c.1768C>T (p.Leu590=)
c.1780C>T (p.Leu594=)
c.1783C>T (p.Leu595=)
c.1792C>T (p.Leu598=)
c.1789C>T (p.Leu597=)
n.2187C>T
n.2206C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.1805885T>ACA355981911FGFR3c.1787T>A (p.Leu596Gln)
c.*837T>A (n.*837T>A)
c.1445T>A (p.Leu482Gln)
c.1769T>A (p.Leu590Gln)
c.1781T>A (p.Leu594Gln)
c.1784T>A (p.Leu595Gln)
c.1793T>A (p.Leu598Gln)
c.1790T>A (p.Leu597Gln)
n.2188T>A
n.2207T>A
4g.1805885T>CCA355981912FGFR3c.1787T>C (p.Leu596Pro)
c.*837T>C (n.*837T>C)
c.1445T>C (p.Leu482Pro)
c.1769T>C (p.Leu590Pro)
c.1781T>C (p.Leu594Pro)
c.1784T>C (p.Leu595Pro)
c.1793T>C (p.Leu598Pro)
c.1790T>C (p.Leu597Pro)
n.2188T>C
n.2207T>C
4g.1805885T>GCA355981913FGFR3c.1787T>G (p.Leu596Arg)
c.*837T>G (n.*837T>G)
c.1445T>G (p.Leu482Arg)
c.1769T>G (p.Leu590Arg)
c.1781T>G (p.Leu594Arg)
c.1784T>G (p.Leu595Arg)
c.1793T>G (p.Leu598Arg)
c.1790T>G (p.Leu597Arg)
n.2188T>G
n.2207T>G
4g.1805886G>ACA438063155FGFR3c.1788G>A (p.Leu596=)
c.*838G>A (n.*838G>A)
c.1446G>A (p.Leu482=)
c.1770G>A (p.Leu590=)
c.1782G>A (p.Leu594=)
c.1785G>A (p.Leu595=)
c.1794G>A (p.Leu598=)
c.1791G>A (p.Leu597=)
n.2189G>A
n.2208G>A
dbSNP gnomAD v4
4g.1805886G>CCA438063157FGFR3c.1788G>C (p.Leu596=)
c.*838G>C (n.*838G>C)
c.1446G>C (p.Leu482=)
c.1770G>C (p.Leu590=)
c.1782G>C (p.Leu594=)
c.1785G>C (p.Leu595=)
c.1794G>C (p.Leu598=)
c.1791G>C (p.Leu597=)
n.2189G>C
n.2208G>C
4g.1805886G=CA1433507672FGFR3c.1788G= (p.Leu596=)
c.*838G= (n.*838G=)
c.1446G= (p.Leu482=)
c.1770G= (p.Leu590=)
c.1782G= (p.Leu594=)
c.1785G= (p.Leu595=)
c.1794G= (p.Leu598=)
c.1791G= (p.Leu597=)
n.2189G=
n.2208G=
4g.1805886G>TCA438063156FGFR3c.1788G>T (p.Leu596=)
c.*838G>T (n.*838G>T)
c.1446G>T (p.Leu482=)
c.1770G>T (p.Leu590=)
c.1782G>T (p.Leu594=)
c.1785G>T (p.Leu595=)
c.1794G>T (p.Leu598=)
c.1791G>T (p.Leu597=)
n.2189G>T
n.2208G>T
4g.1805887G>ACA355981914FGFR3c.1789G>A (p.Val597Met)
c.*839G>A (n.*839G>A)
c.1447G>A (p.Val483Met)
c.1771G>A (p.Val591Met)
c.1783G>A (p.Val595Met)
c.1786G>A (p.Val596Met)
c.1795G>A (p.Val599Met)
c.1792G>A (p.Val598Met)
n.2190G>A
n.2209G>A
4g.1805887G>CCA355981915FGFR3c.1789G>C (p.Val597Leu)
c.*839G>C (n.*839G>C)
c.1447G>C (p.Val483Leu)
c.1771G>C (p.Val591Leu)
c.1783G>C (p.Val595Leu)
c.1786G>C (p.Val596Leu)
c.1795G>C (p.Val599Leu)
c.1792G>C (p.Val598Leu)
n.2190G>C
n.2209G>C
gnomAD v4
4g.1805887G>TCA355981916FGFR3c.1789G>T (p.Val597Leu)
c.*839G>T (n.*839G>T)
c.1447G>T (p.Val483Leu)
c.1771G>T (p.Val591Leu)
c.1783G>T (p.Val595Leu)
c.1786G>T (p.Val596Leu)
c.1795G>T (p.Val599Leu)
c.1792G>T (p.Val598Leu)
n.2190G>T
n.2209G>T
gnomAD v4
4g.1805888T>ACA355981917FGFR3c.1790T>A (p.Val597Glu)
c.*840T>A (n.*840T>A)
c.1448T>A (p.Val483Glu)
c.1772T>A (p.Val591Glu)
c.1784T>A (p.Val595Glu)
c.1787T>A (p.Val596Glu)
c.1796T>A (p.Val599Glu)
c.1793T>A (p.Val598Glu)
n.2191T>A
n.2210T>A
4g.1805888T>CCA355981918FGFR3c.1790T>C (p.Val597Ala)
c.*840T>C (n.*840T>C)
c.1448T>C (p.Val483Ala)
c.1772T>C (p.Val591Ala)
c.1784T>C (p.Val595Ala)
c.1787T>C (p.Val596Ala)
c.1796T>C (p.Val599Ala)
c.1793T>C (p.Val598Ala)
n.2191T>C
n.2210T>C
4g.1805888T>GCA355981919FGFR3c.1790T>G (p.Val597Gly)
c.*840T>G (n.*840T>G)
c.1448T>G (p.Val483Gly)
c.1772T>G (p.Val591Gly)
c.1784T>G (p.Val595Gly)
c.1787T>G (p.Val596Gly)
c.1796T>G (p.Val599Gly)
c.1793T>G (p.Val598Gly)
n.2191T>G
n.2210T>G
4g.1805889G>ACA438063158FGFR3c.1791G>A (p.Val597=)
c.*841G>A (n.*841G>A)
c.1449G>A (p.Val483=)
c.1773G>A (p.Val591=)
c.1785G>A (p.Val595=)
c.1788G>A (p.Val596=)
c.1797G>A (p.Val599=)
c.1794G>A (p.Val598=)
n.2192G>A
n.2211G>A
4g.1805889G>CCA438063160FGFR3c.1791G>C (p.Val597=)
c.*841G>C (n.*841G>C)
c.1449G>C (p.Val483=)
c.1773G>C (p.Val591=)
c.1785G>C (p.Val595=)
c.1788G>C (p.Val596=)
c.1797G>C (p.Val599=)
c.1794G>C (p.Val598=)
n.2192G>C
n.2211G>C
4g.1805889G>TCA438063159FGFR3c.1791G>T (p.Val597=)
c.*841G>T (n.*841G>T)
c.1449G>T (p.Val483=)
c.1773G>T (p.Val591=)
c.1785G>T (p.Val595=)
c.1788G>T (p.Val596=)
c.1797G>T (p.Val599=)
c.1794G>T (p.Val598=)
n.2192G>T
n.2211G>T
4g.1805890T>ACA355981920FGFR3c.1792T>A (p.Ser598Thr)
c.*842T>A (n.*842T>A)
c.1450T>A (p.Ser484Thr)
c.1774T>A (p.Ser592Thr)
c.1786T>A (p.Ser596Thr)
c.1789T>A (p.Ser597Thr)
c.1798T>A (p.Ser600Thr)
c.1795T>A (p.Ser599Thr)
n.2193T>A
n.2212T>A
4g.1805890T>CCA355981921FGFR3c.1792T>C (p.Ser598Pro)
c.*842T>C (n.*842T>C)
c.1450T>C (p.Ser484Pro)
c.1774T>C (p.Ser592Pro)
c.1786T>C (p.Ser596Pro)
c.1789T>C (p.Ser597Pro)
c.1798T>C (p.Ser600Pro)
c.1795T>C (p.Ser599Pro)
n.2193T>C
n.2212T>C
4g.1805890T>GCA355981922FGFR3c.1792T>G (p.Ser598Ala)
c.*842T>G (n.*842T>G)
c.1450T>G (p.Ser484Ala)
c.1774T>G (p.Ser592Ala)
c.1786T>G (p.Ser596Ala)
c.1789T>G (p.Ser597Ala)
c.1798T>G (p.Ser600Ala)
c.1795T>G (p.Ser599Ala)
n.2193T>G
n.2212T>G
4g.1805891C>ACA355981923FGFR3c.1793C>A (p.Ser598Tyr)
c.*843C>A (n.*843C>A)
c.1451C>A (p.Ser484Tyr)
c.1775C>A (p.Ser592Tyr)
c.1787C>A (p.Ser596Tyr)
c.1790C>A (p.Ser597Tyr)
c.1799C>A (p.Ser600Tyr)
c.1796C>A (p.Ser599Tyr)
n.2194C>A
n.2213C>A
4g.1805891C>GCA355981925FGFR3c.1793C>G (p.Ser598Cys)
c.*843C>G (n.*843C>G)
c.1451C>G (p.Ser484Cys)
c.1775C>G (p.Ser592Cys)
c.1787C>G (p.Ser596Cys)
c.1790C>G (p.Ser597Cys)
c.1799C>G (p.Ser600Cys)
c.1796C>G (p.Ser599Cys)
n.2194C>G
n.2213C>G
dbSNP
4g.1805891C>TCA355981924FGFR3c.1793C>T (p.Ser598Phe)
c.*843C>T (n.*843C>T)
c.1451C>T (p.Ser484Phe)
c.1775C>T (p.Ser592Phe)
c.1787C>T (p.Ser596Phe)
c.1790C>T (p.Ser597Phe)
c.1799C>T (p.Ser600Phe)
c.1796C>T (p.Ser599Phe)
n.2194C>T
n.2213C>T
4g.1805892C>ACA438063168FGFR3c.1794C>A (p.Ser598=)
c.*844C>A (n.*844C>A)
c.1452C>A (p.Ser484=)
c.1776C>A (p.Ser592=)
c.1788C>A (p.Ser596=)
c.1791C>A (p.Ser597=)
c.1800C>A (p.Ser600=)
c.1797C>A (p.Ser599=)
n.2195C>A
n.2214C>A
4g.1805892C=CA1433507673FGFR3c.1794C= (p.Ser598=)
c.*844C= (n.*844C=)
c.1452C= (p.Ser484=)
c.1776C= (p.Ser592=)
c.1788C= (p.Ser596=)
c.1791C= (p.Ser597=)
c.1800C= (p.Ser600=)
c.1797C= (p.Ser599=)
n.2195C=
n.2214C=
4g.1805892C>GCA438063166FGFR3c.1794C>G (p.Ser598=)
c.*844C>G (n.*844C>G)
c.1452C>G (p.Ser484=)
c.1776C>G (p.Ser592=)
c.1788C>G (p.Ser596=)
c.1791C>G (p.Ser597=)
c.1800C>G (p.Ser600=)
c.1797C>G (p.Ser599=)
n.2195C>G
n.2214C>G
gnomAD v4
4g.1805892C>TCA438063167FGFR3c.1794C>T (p.Ser598=)
c.*844C>T (n.*844C>T)
c.1452C>T (p.Ser484=)
c.1776C>T (p.Ser592=)
c.1788C>T (p.Ser596=)
c.1791C>T (p.Ser597=)
c.1800C>T (p.Ser600=)
c.1797C>T (p.Ser599=)
n.2195C>T
n.2214C>T
dbSNP gnomAD v4
4g.1805893T>ACA355981926FGFR3c.1795T>A (p.Cys599Ser)
c.*845T>A (n.*845T>A)
c.1453T>A (p.Cys485Ser)
c.1777T>A (p.Cys593Ser)
c.1789T>A (p.Cys597Ser)
c.1792T>A (p.Cys598Ser)
c.1801T>A (p.Cys601Ser)
c.1798T>A (p.Cys600Ser)
n.2196T>A
n.2215T>A

Number of alleles fetched