Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.140753332_140753333insTTCACTGTAGCTAGACCATCGAGACA891842051BRAFc.1784_1785insTGGTCTAGCTACAGTGAATCTCGA (p.Val600_Lys601insAsnLeuAspGlyLeuAlaThrVal)
n.68_69insTGGTCTAGCTACAGTGAATCTCGA (p.Val28_Lys29insAsnLeuAspGlyLeuAlaThrVal)
n.1819_1820insTGGTCTAGCTACAGTGAATCTCGA (p.=)
c.1695-3933_1695-3932insTGGTCTAGCTACAGTGAATCTCGA (p.=)
c.1904_1905insTGGTCTAGCTACAGTGAATCTCGA (p.Val640_Lys641insAsnLeuAspGlyLeuAlaThrVal)
c.1793_1794insTGGTCTAGCTACAGTGAATCTCGA (p.Val603_Lys604insAsnLeuAspGlyLeuAlaThrVal)
c.1718_1719insTGGTCTAGCTACAGTGAATCTCGA (p.Val578_Lys579insAsnLeuAspGlyLeuAlaThrVal)
c.1682_1683insTGGTCTAGCTACAGTGAATCTCGA (p.Val566_Lys567insAsnLeuAspGlyLeuAlaThrVal)
c.1673_1674insTGGTCTAGCTACAGTGAATCTCGA (p.Val563_Lys564insAsnLeuAspGlyLeuAlaThrVal)
c.1628_1629insTGGTCTAGCTACAGTGAATCTCGA (p.Val548_Lys549insAsnLeuAspGlyLeuAlaThrVal)
c.1520_1521insTGGTCTAGCTACAGTGAATCTCGA (p.Val512_Lys513insAsnLeuAspGlyLeuAlaThrVal)
7g.140753338_140753355dupCA645544101BRAFc.1781_1798dup (p.Thr599_Val600insAspPheGlyLeuAlaThr)
n.65_82dup (p.Thr27_Val28insAspPheGlyLeuAlaThr)
n.1816_1833dup (p.=)
c.1695-3936_1695-3919dup (p.=)
c.1901_1918dup (p.Thr639_Val640insAspPheGlyLeuAlaThr)
c.1790_1807dup (p.Thr602_Val603insAspPheGlyLeuAlaThr)
c.1715_1732dup (p.Thr577_Val578insAspPheGlyLeuAlaThr)
c.1679_1696dup (p.Thr565_Val566insAspPheGlyLeuAlaThr)
c.1670_1687dup (p.Thr562_Val563insAspPheGlyLeuAlaThr)
c.1625_1642dup (p.Thr547_Val548insAspPheGlyLeuAlaThr)
c.1517_1534dup (p.Thr511_Val512insAspPheGlyLeuAlaThr)
COSMIC
7g.140753339_140753353delCA891842052BRAFc.1782_1796del (p.Asp594_Thr599delinsGlu)
n.66_80del (p.Asp22_Thr27delinsGlu)
n.1817_1831del (p.=)
c.1695-3935_1695-3921del (p.=)
c.1902_1916del (p.Asp634_Thr639delinsGlu)
c.1791_1805del (p.Asp597_Thr602delinsGlu)
c.1716_1730del (p.Asp572_Thr577delinsGlu)
c.1680_1694del (p.Asp560_Thr565delinsGlu)
c.1671_1685del (p.Asp557_Thr562delinsGlu)
c.1626_1640del (p.Asp542_Thr547delinsGlu)
c.1518_1532del (p.Asp506_Thr511delinsGlu)
7g.140753339_140753340insTAGCTAGACCAAAATCACCTATTTTTTCA645544107BRAFc.1769_1770insAAAAATAGGTGATTTTGGTCTAGCTAA (p.Ala598_Thr599insLysLysIleGlyAspPheGlyLeuAla)
n.53_54insAAAAATAGGTGATTTTGGTCTAGCTAA (p.Ala26_Thr27insLysLysIleGlyAspPheGlyLeuAla)
n.1804_1805insAAAAATAGGTGATTTTGGTCTAGCTAA (p.=)
c.1695-3948_1695-3947insAAAAATAGGTGATTTTGGTCTAGCTAA (p.=)
c.1889_1890insAAAAATAGGTGATTTTGGTCTAGCTAA (p.Ala638_Thr639insLysLysIleGlyAspPheGlyLeuAla)
c.1778_1779insAAAAATAGGTGATTTTGGTCTAGCTAA (p.Ala601_Thr602insLysLysIleGlyAspPheGlyLeuAla)
c.1703_1704insAAAAATAGGTGATTTTGGTCTAGCTAA (p.Ala576_Thr577insLysLysIleGlyAspPheGlyLeuAla)
c.1667_1668insAAAAATAGGTGATTTTGGTCTAGCTAA (p.Ala564_Thr565insLysLysIleGlyAspPheGlyLeuAla)
c.1658_1659insAAAAATAGGTGATTTTGGTCTAGCTAA (p.Ala561_Thr562insLysLysIleGlyAspPheGlyLeuAla)
c.1613_1614insAAAAATAGGTGATTTTGGTCTAGCTAA (p.Ala546_Thr547insLysLysIleGlyAspPheGlyLeuAla)
c.1505_1506insAAAAATAGGTGATTTTGGTCTAGCTAA (p.Ala510_Thr511insLysLysIleGlyAspPheGlyLeuAla)
COSMIC
7g.140753345_140753346delinsGACA16602421BRAFc.1789_1790delinsTC (p.Leu597Ser)
n.73_74delinsTC (p.Leu25Ser)
n.1824_1825delinsTC (p.=)
c.1695-3928_1695-3927delinsTC (p.=)
c.1909_1910delinsTC (p.Leu637Ser)
c.1798_1799delinsTC (p.Leu600Ser)
c.1723_1724delinsTC (p.Leu575Ser)
c.1687_1688delinsTC (p.Leu563Ser)
c.1678_1679delinsTC (p.Leu560Ser)
c.1633_1634delinsTC (p.Leu545Ser)
c.1525_1526delinsTC (p.Leu509Ser)
ClinVar dbSNP COSMIC
7g.140753345_140753347dupCA891842034BRAFc.1788_1790dup (p.Leu597_Ala598insLeu)
n.72_74dup (p.Leu25_Ala26insLeu)
n.1823_1825dup (p.=)
c.1695-3929_1695-3927dup (p.=)
c.1908_1910dup (p.Leu637_Ala638insLeu)
c.1797_1799dup (p.Leu600_Ala601insLeu)
c.1722_1724dup (p.Leu575_Ala576insLeu)
c.1686_1688dup (p.Leu563_Ala564insLeu)
c.1677_1679dup (p.Leu560_Ala561insLeu)
c.1632_1634dup (p.Leu545_Ala546insLeu)
c.1524_1526dup (p.Leu509_Ala510insLeu)
7g.140753346G>ACA168047474BRAFc.1789C>T (p.Leu597=)
n.73C>T (p.Leu25=)
n.1824C>T (p.=)
c.1695-3928C>T (p.=)
c.1909C>T (p.Leu637=)
c.1798C>T (p.Leu600=)
c.1723C>T (p.Leu575=)
c.1687C>T (p.Leu563=)
c.1678C>T (p.Leu560=)
c.1633C>T (p.Leu545=)
c.1525C>T (p.Leu509=)
dbSNP gnomAD COSMIC
7g.140753346G>CCA123651BRAFc.1789C>G (p.Leu597Val)
n.73C>G (p.Leu25Val)
n.1824C>G (p.=)
c.1695-3928C>G (p.=)
c.1909C>G (p.Leu637Val)
c.1798C>G (p.Leu600Val)
c.1723C>G (p.Leu575Val)
c.1687C>G (p.Leu563Val)
c.1678C>G (p.Leu560Val)
c.1633C>G (p.Leu545Val)
c.1525C>G (p.Leu509Val)
ClinVar dbSNP COSMIC
7g.140753346G>TCA369543117BRAFc.1789C>A (p.Leu597Ile)
n.73C>A (p.Leu25Ile)
n.1824C>A (p.=)
c.1695-3928C>A (p.=)
c.1909C>A (p.Leu637Ile)
c.1798C>A (p.Leu600Ile)
c.1723C>A (p.Leu575Ile)
c.1687C>A (p.Leu563Ile)
c.1678C>A (p.Leu560Ile)
c.1633C>A (p.Leu545Ile)
c.1525C>A (p.Leu509Ile)
7g.140753347A>CCA457986988BRAFc.1788T>G (p.Gly596=)
n.72T>G (p.Gly24=)
n.1823T>G (p.=)
c.1695-3929T>G (p.=)
c.1908T>G (p.Gly636=)
c.1797T>G (p.Gly599=)
c.1722T>G (p.Gly574=)
c.1686T>G (p.Gly562=)
c.1677T>G (p.Gly559=)
c.1632T>G (p.Gly544=)
c.1524T>G (p.Gly508=)
7g.140753347A>GCA457986990BRAFc.1788T>C (p.Gly596=)
n.72T>C (p.Gly24=)
n.1823T>C (p.=)
c.1695-3929T>C (p.=)
c.1908T>C (p.Gly636=)
c.1797T>C (p.Gly599=)
c.1722T>C (p.Gly574=)
c.1686T>C (p.Gly562=)
c.1677T>C (p.Gly559=)
c.1632T>C (p.Gly544=)
c.1524T>C (p.Gly508=)
7g.140753347A>TCA457986991BRAFc.1788T>A (p.Gly596=)
n.72T>A (p.Gly24=)
n.1823T>A (p.=)
c.1695-3929T>A (p.=)
c.1908T>A (p.Gly636=)
c.1797T>A (p.Gly599=)
c.1722T>A (p.Gly574=)
c.1686T>A (p.Gly562=)
c.1677T>A (p.Gly559=)
c.1632T>A (p.Gly544=)
c.1524T>A (p.Gly508=)
7g.140753348C>ACA220161BRAFc.1787G>T (p.Gly596Val)
n.71G>T (p.Gly24Val)
n.1822G>T (p.=)
c.1695-3930G>T (p.=)
c.1907G>T (p.Gly636Val)
c.1796G>T (p.Gly599Val)
c.1721G>T (p.Gly574Val)
c.1685G>T (p.Gly562Val)
c.1676G>T (p.Gly559Val)
c.1631G>T (p.Gly544Val)
c.1523G>T (p.Gly508Val)
ClinVar dbSNP
7g.140753348C>GCA369543122BRAFc.1787G>C (p.Gly596Ala)
n.71G>C (p.Gly24Ala)
n.1822G>C (p.=)
c.1695-3930G>C (p.=)
c.1907G>C (p.Gly636Ala)
c.1796G>C (p.Gly599Ala)
c.1721G>C (p.Gly574Ala)
c.1685G>C (p.Gly562Ala)
c.1676G>C (p.Gly559Ala)
c.1631G>C (p.Gly544Ala)
c.1523G>C (p.Gly508Ala)
7g.140753348C>TCA16602814BRAFc.1787G>A (p.Gly596Asp)
n.71G>A (p.Gly24Asp)
n.1822G>A (p.=)
c.1695-3930G>A (p.=)
c.1907G>A (p.Gly636Asp)
c.1796G>A (p.Gly599Asp)
c.1721G>A (p.Gly574Asp)
c.1685G>A (p.Gly562Asp)
c.1676G>A (p.Gly559Asp)
c.1631G>A (p.Gly544Asp)
c.1523G>A (p.Gly508Asp)
ClinVar COSMIC
7g.140753348delCA457986993BRAFc.1786del (p.Gly596ValfsTer2)
n.70del (p.Gly24ValfsTer2)
n.1821del (p.=)
c.1695-3931del (p.=)
c.1906del (p.Gly636ValfsTer2)
c.1795del (p.Gly599ValfsTer2)
c.1720del (p.Gly574ValfsTer2)
c.1684del (p.Gly562ValfsTer2)
c.1675del (p.Gly559ValfsTer2)
c.1630del (p.Gly544ValfsTer2)
c.1522del (p.Gly508ValfsTer2)
COSMIC
7g.140753349C>ACA135098BRAFc.1786G>T (p.Gly596Cys)
n.70G>T (p.Gly24Cys)
n.1821G>T (p.=)
c.1695-3931G>T (p.=)
c.1906G>T (p.Gly636Cys)
c.1795G>T (p.Gly599Cys)
c.1720G>T (p.Gly574Cys)
c.1684G>T (p.Gly562Cys)
c.1675G>T (p.Gly559Cys)
c.1630G>T (p.Gly544Cys)
c.1522G>T (p.Gly508Cys)
ClinVar dbSNP
7g.140753349C>GCA16602422BRAFc.1786G>C (p.Gly596Arg)
n.70G>C (p.Gly24Arg)
n.1821G>C (p.=)
c.1695-3931G>C (p.=)
c.1906G>C (p.Gly636Arg)
c.1795G>C (p.Gly599Arg)
c.1720G>C (p.Gly574Arg)
c.1684G>C (p.Gly562Arg)
c.1675G>C (p.Gly559Arg)
c.1630G>C (p.Gly544Arg)
c.1522G>C (p.Gly508Arg)
ClinVar dbSNP COSMIC
7g.140753349C>TCA16602813BRAFc.1786G>A (p.Gly596Ser)
n.70G>A (p.Gly24Ser)
n.1821G>A (p.=)
c.1695-3931G>A (p.=)
c.1906G>A (p.Gly636Ser)
c.1795G>A (p.Gly599Ser)
c.1720G>A (p.Gly574Ser)
c.1684G>A (p.Gly562Ser)
c.1675G>A (p.Gly559Ser)
c.1630G>A (p.Gly544Ser)
c.1522G>A (p.Gly508Ser)
ClinVar
7g.140753350A>CCA280058BRAFc.1785T>G (p.Phe595Leu)
n.69T>G (p.Phe23Leu)
n.1820T>G (p.=)
c.1695-3932T>G (p.=)
c.1905T>G (p.Phe635Leu)
c.1794T>G (p.Phe598Leu)
c.1719T>G (p.Phe573Leu)
c.1683T>G (p.Phe561Leu)
c.1674T>G (p.Phe558Leu)
c.1629T>G (p.Phe543Leu)
c.1521T>G (p.Phe507Leu)
ClinVar dbSNP COSMIC
7g.140753350A>GCA457986995BRAFc.1785T>C (p.Phe595=)
n.69T>C (p.Phe23=)
n.1820T>C (p.=)
c.1695-3932T>C (p.=)
c.1905T>C (p.Phe635=)
c.1794T>C (p.Phe598=)
c.1719T>C (p.Phe573=)
c.1683T>C (p.Phe561=)
c.1674T>C (p.Phe558=)
c.1629T>C (p.Phe543=)
c.1521T>C (p.Phe507=)
7g.140753350A>TCA295915BRAFc.1785T>A (p.Phe595Leu)
n.69T>A (p.Phe23Leu)
n.1820T>A (p.=)
c.1695-3932T>A (p.=)
c.1905T>A (p.Phe635Leu)
c.1794T>A (p.Phe598Leu)
c.1719T>A (p.Phe573Leu)
c.1683T>A (p.Phe561Leu)
c.1674T>A (p.Phe558Leu)
c.1629T>A (p.Phe543Leu)
c.1521T>A (p.Phe507Leu)
ClinVar dbSNP COSMIC
7g.140753351A>CCA369543137BRAFc.1784T>G (p.Phe595Cys)
n.68T>G (p.Phe23Cys)
n.1819T>G (p.=)
c.1695-3933T>G (p.=)
c.1904T>G (p.Phe635Cys)
c.1793T>G (p.Phe598Cys)
c.1718T>G (p.Phe573Cys)
c.1682T>G (p.Phe561Cys)
c.1673T>G (p.Phe558Cys)
c.1628T>G (p.Phe543Cys)
c.1520T>G (p.Phe507Cys)
7g.140753351A>GCA16602738BRAFc.1784T>C (p.Phe595Ser)
n.68T>C (p.Phe23Ser)
n.1819T>C (p.=)
c.1695-3933T>C (p.=)
c.1904T>C (p.Phe635Ser)
c.1793T>C (p.Phe598Ser)
c.1718T>C (p.Phe573Ser)
c.1682T>C (p.Phe561Ser)
c.1673T>C (p.Phe558Ser)
c.1628T>C (p.Phe543Ser)
c.1520T>C (p.Phe507Ser)
ClinVar dbSNP COSMIC
7g.140753351A>TCA369543141BRAFc.1784T>A (p.Phe595Tyr)
n.68T>A (p.Phe23Tyr)
n.1819T>A (p.=)
c.1695-3933T>A (p.=)
c.1904T>A (p.Phe635Tyr)
c.1793T>A (p.Phe598Tyr)
c.1718T>A (p.Phe573Tyr)
c.1682T>A (p.Phe561Tyr)
c.1673T>A (p.Phe558Tyr)
c.1628T>A (p.Phe543Tyr)
c.1520T>A (p.Phe507Tyr)
7g.140753352A>CCA369543142BRAFc.1783T>G (p.Phe595Val)
n.67T>G (p.Phe23Val)
n.1818T>G (p.=)
c.1695-3934T>G (p.=)
c.1903T>G (p.Phe635Val)
c.1792T>G (p.Phe598Val)
c.1717T>G (p.Phe573Val)
c.1681T>G (p.Phe561Val)
c.1672T>G (p.Phe558Val)
c.1627T>G (p.Phe543Val)
c.1519T>G (p.Phe507Val)
7g.140753352A>GCA280071BRAFc.1783T>C (p.Phe595Leu)
n.67T>C (p.Phe23Leu)
n.1818T>C (p.=)
c.1695-3934T>C (p.=)
c.1903T>C (p.Phe635Leu)
c.1792T>C (p.Phe598Leu)
c.1717T>C (p.Phe573Leu)
c.1681T>C (p.Phe561Leu)
c.1672T>C (p.Phe558Leu)
c.1627T>C (p.Phe543Leu)
c.1519T>C (p.Phe507Leu)
ClinVar dbSNP COSMIC
7g.140753352A>TCA369543144BRAFc.1783T>A (p.Phe595Ile)
n.67T>A (p.Phe23Ile)
n.1818T>A (p.=)
c.1695-3934T>A (p.=)
c.1903T>A (p.Phe635Ile)
c.1792T>A (p.Phe598Ile)
c.1717T>A (p.Phe573Ile)
c.1681T>A (p.Phe561Ile)
c.1672T>A (p.Phe558Ile)
c.1627T>A (p.Phe543Ile)
c.1519T>A (p.Phe507Ile)
7g.140753353A>CCA16602423BRAFc.1782T>G (p.Asp594Glu)
n.66T>G (p.Asp22Glu)
n.1817T>G (p.=)
c.1695-3935T>G (p.=)
c.1902T>G (p.Asp634Glu)
c.1791T>G (p.Asp597Glu)
c.1716T>G (p.Asp572Glu)
c.1680T>G (p.Asp560Glu)
c.1671T>G (p.Asp557Glu)
c.1626T>G (p.Asp542Glu)
c.1518T>G (p.Asp506Glu)
ClinVar COSMIC
7g.140753353A>GCA457987004BRAFc.1782T>C (p.Asp594=)
n.66T>C (p.Asp22=)
n.1817T>C (p.=)
c.1695-3935T>C (p.=)
c.1902T>C (p.Asp634=)
c.1791T>C (p.Asp597=)
c.1716T>C (p.Asp572=)
c.1680T>C (p.Asp560=)
c.1671T>C (p.Asp557=)
c.1626T>C (p.Asp542=)
c.1518T>C (p.Asp506=)
COSMIC
7g.140753353A>TCA16602424BRAFc.1782T>A (p.Asp594Glu)
n.66T>A (p.Asp22Glu)
n.1817T>A (p.=)
c.1695-3935T>A (p.=)
c.1902T>A (p.Asp634Glu)
c.1791T>A (p.Asp597Glu)
c.1716T>A (p.Asp572Glu)
c.1680T>A (p.Asp560Glu)
c.1671T>A (p.Asp557Glu)
c.1626T>A (p.Asp542Glu)
c.1518T>A (p.Asp506Glu)
ClinVar dbSNP COSMIC
7g.140753354T>ACA16602425BRAFc.1781A>T (p.Asp594Val)
n.65A>T (p.Asp22Val)
n.1816A>T (p.=)
c.1695-3936A>T (p.=)
c.1901A>T (p.Asp634Val)
c.1790A>T (p.Asp597Val)
c.1715A>T (p.Asp572Val)
c.1679A>T (p.Asp560Val)
c.1670A>T (p.Asp557Val)
c.1625A>T (p.Asp542Val)
c.1517A>T (p.Asp506Val)
ClinVar dbSNP COSMIC
7g.140753354T>CCA123657BRAFc.1781A>G (p.Asp594Gly)
n.65A>G (p.Asp22Gly)
n.1816A>G (p.=)
c.1695-3936A>G (p.=)
c.1901A>G (p.Asp634Gly)
c.1790A>G (p.Asp597Gly)
c.1715A>G (p.Asp572Gly)
c.1679A>G (p.Asp560Gly)
c.1670A>G (p.Asp557Gly)
c.1625A>G (p.Asp542Gly)
c.1517A>G (p.Asp506Gly)
ClinVar dbSNP COSMIC
7g.140753354T>GCA16602532BRAFc.1781A>C (p.Asp594Ala)
n.65A>C (p.Asp22Ala)
n.1816A>C (p.=)
c.1695-3936A>C (p.=)
c.1901A>C (p.Asp634Ala)
c.1790A>C (p.Asp597Ala)
c.1715A>C (p.Asp572Ala)
c.1679A>C (p.Asp560Ala)
c.1670A>C (p.Asp557Ala)
c.1625A>C (p.Asp542Ala)
c.1517A>C (p.Asp506Ala)
ClinVar COSMIC
7g.140753354_140753357delinsCCAGCA891842036BRAFc.1778_1781delinsCTGG (p.Gly593_Asp594delinsAlaGly)
n.62_65delinsCTGG (p.Gly21_Asp22delinsAlaGly)
n.1813_1816delinsCTGG (p.=)
c.1695-3939_1695-3936delinsCTGG (p.=)
c.1898_1901delinsCTGG (p.Gly633_Asp634delinsAlaGly)
c.1787_1790delinsCTGG (p.Gly596_Asp597delinsAlaGly)
c.1712_1715delinsCTGG (p.Gly571_Asp572delinsAlaGly)
c.1676_1679delinsCTGG (p.Gly559_Asp560delinsAlaGly)
c.1667_1670delinsCTGG (p.Gly556_Asp557delinsAlaGly)
c.1622_1625delinsCTGG (p.Gly541_Asp542delinsAlaGly)
c.1514_1517delinsCTGG (p.Gly505_Asp506delinsAlaGly)
7g.140753355C>ACA369543156BRAFc.1780G>T (p.Asp594Tyr)
n.64G>T (p.Asp22Tyr)
n.1815G>T (p.=)
c.1695-3937G>T (p.=)
c.1900G>T (p.Asp634Tyr)
c.1789G>T (p.Asp597Tyr)
c.1714G>T (p.Asp572Tyr)
c.1678G>T (p.Asp560Tyr)
c.1669G>T (p.Asp557Tyr)
c.1624G>T (p.Asp542Tyr)
c.1516G>T (p.Asp506Tyr)
7g.140753355C>GCA16602426BRAFc.1780G>C (p.Asp594His)
n.64G>C (p.Asp22His)
n.1815G>C (p.=)
c.1695-3937G>C (p.=)
c.1900G>C (p.Asp634His)
c.1789G>C (p.Asp597His)
c.1714G>C (p.Asp572His)
c.1678G>C (p.Asp560His)
c.1669G>C (p.Asp557His)
c.1624G>C (p.Asp542His)
c.1516G>C (p.Asp506His)
ClinVar COSMIC
7g.140753355C>TCA135095BRAFc.1780G>A (p.Asp594Asn)
n.64G>A (p.Asp22Asn)
n.1815G>A (p.=)
c.1695-3937G>A (p.=)
c.1900G>A (p.Asp634Asn)
c.1789G>A (p.Asp597Asn)
c.1714G>A (p.Asp572Asn)
c.1678G>A (p.Asp560Asn)
c.1669G>A (p.Asp557Asn)
c.1624G>A (p.Asp542Asn)
c.1516G>A (p.Asp506Asn)
ClinVar dbSNP COSMIC
7g.140753355_140753356delinsTCCA16602427BRAFc.1779_1780delinsGA (p.Asp594Asn)
n.63_64delinsGA (p.Asp22Asn)
n.1814_1815delinsGA (p.=)
c.1695-3938_1695-3937delinsGA (p.=)
c.1899_1900delinsGA (p.Asp634Asn)
c.1788_1789delinsGA (p.Asp597Asn)
c.1713_1714delinsGA (p.Asp572Asn)
c.1677_1678delinsGA (p.Asp560Asn)
c.1668_1669delinsGA (p.Asp557Asn)
c.1623_1624delinsGA (p.Asp542Asn)
c.1515_1516delinsGA (p.Asp506Asn)
ClinVar dbSNP COSMIC
7g.140753356A>CCA457987011BRAFc.1779T>G (p.Gly593=)
n.63T>G (p.Gly21=)
n.1814T>G (p.=)
c.1695-3938T>G (p.=)
c.1899T>G (p.Gly633=)
c.1788T>G (p.Gly596=)
c.1713T>G (p.Gly571=)
c.1677T>G (p.Gly559=)
c.1668T>G (p.Gly556=)
c.1623T>G (p.Gly541=)
c.1515T>G (p.Gly505=)
7g.140753356A>GCA457987012BRAFc.1779T>C (p.Gly593=)
n.63T>C (p.Gly21=)
n.1814T>C (p.=)
c.1695-3938T>C (p.=)
c.1899T>C (p.Gly633=)
c.1788T>C (p.Gly596=)
c.1713T>C (p.Gly571=)
c.1677T>C (p.Gly559=)
c.1668T>C (p.Gly556=)
c.1623T>C (p.Gly541=)
c.1515T>C (p.Gly505=)
7g.140753356A>TCA457987013BRAFc.1779T>A (p.Gly593=)
n.63T>A (p.Gly21=)
n.1814T>A (p.=)
c.1695-3938T>A (p.=)
c.1899T>A (p.Gly633=)
c.1788T>A (p.Gly596=)
c.1713T>A (p.Gly571=)
c.1677T>A (p.Gly559=)
c.1668T>A (p.Gly556=)
c.1623T>A (p.Gly541=)
c.1515T>A (p.Gly505=)
7g.140753357C>ACA369543160BRAFc.1778G>T (p.Gly593Val)
n.62G>T (p.Gly21Val)
n.1813G>T (p.=)
c.1695-3939G>T (p.=)
c.1898G>T (p.Gly633Val)
c.1787G>T (p.Gly596Val)
c.1712G>T (p.Gly571Val)
c.1676G>T (p.Gly559Val)
c.1667G>T (p.Gly556Val)
c.1622G>T (p.Gly541Val)
c.1514G>T (p.Gly505Val)
7g.140753357C>GCA369543161BRAFc.1778G>C (p.Gly593Ala)
n.62G>C (p.Gly21Ala)
n.1813G>C (p.=)
c.1695-3939G>C (p.=)
c.1898G>C (p.Gly633Ala)
c.1787G>C (p.Gly596Ala)
c.1712G>C (p.Gly571Ala)
c.1676G>C (p.Gly559Ala)
c.1667G>C (p.Gly556Ala)
c.1622G>C (p.Gly541Ala)
c.1514G>C (p.Gly505Ala)
7g.140753357C>TCA369543163BRAFc.1778G>A (p.Gly593Asp)
n.62G>A (p.Gly21Asp)
n.1813G>A (p.=)
c.1695-3939G>A (p.=)
c.1898G>A (p.Gly633Asp)
c.1787G>A (p.Gly596Asp)
c.1712G>A (p.Gly571Asp)
c.1676G>A (p.Gly559Asp)
c.1667G>A (p.Gly556Asp)
c.1622G>A (p.Gly541Asp)
c.1514G>A (p.Gly505Asp)
COSMIC
7g.140753358C>ACA369543165BRAFc.1777G>T (p.Gly593Cys)
n.61G>T (p.Gly21Cys)
n.1812G>T (p.=)
c.1695-3940G>T (p.=)
c.1897G>T (p.Gly633Cys)
c.1786G>T (p.Gly596Cys)
c.1711G>T (p.Gly571Cys)
c.1675G>T (p.Gly559Cys)
c.1666G>T (p.Gly556Cys)
c.1621G>T (p.Gly541Cys)
c.1513G>T (p.Gly505Cys)
7g.140753358C>GCA369543167BRAFc.1777G>C (p.Gly593Arg)
n.61G>C (p.Gly21Arg)
n.1812G>C (p.=)
c.1695-3940G>C (p.=)
c.1897G>C (p.Gly633Arg)
c.1786G>C (p.Gly596Arg)
c.1711G>C (p.Gly571Arg)
c.1675G>C (p.Gly559Arg)
c.1666G>C (p.Gly556Arg)
c.1621G>C (p.Gly541Arg)
c.1513G>C (p.Gly505Arg)
7g.140753358C>TCA369543170BRAFc.1777G>A (p.Gly593Ser)
n.61G>A (p.Gly21Ser)
n.1812G>A (p.=)
c.1695-3940G>A (p.=)
c.1897G>A (p.Gly633Ser)
c.1786G>A (p.Gly596Ser)
c.1711G>A (p.Gly571Ser)
c.1675G>A (p.Gly559Ser)
c.1666G>A (p.Gly556Ser)
c.1621G>A (p.Gly541Ser)
c.1513G>A (p.Gly505Ser)
COSMIC
7g.140753359T>ACA457987019BRAFc.1776A>T (p.Ile592=)
n.60A>T (p.Ile20=)
n.1811A>T (p.=)
c.1695-3941A>T (p.=)
c.1896A>T (p.Ile632=)
c.1785A>T (p.Ile595=)
c.1710A>T (p.Ile570=)
c.1674A>T (p.Ile558=)
c.1665A>T (p.Ile555=)
c.1620A>T (p.Ile540=)
c.1512A>T (p.Ile504=)
7g.140753359T>CCA16602739BRAFc.1776A>G (p.Ile592Met)
n.60A>G (p.Ile20Met)
n.1811A>G (p.=)
c.1695-3941A>G (p.=)
c.1896A>G (p.Ile632Met)
c.1785A>G (p.Ile595Met)
c.1710A>G (p.Ile570Met)
c.1674A>G (p.Ile558Met)
c.1665A>G (p.Ile555Met)
c.1620A>G (p.Ile540Met)
c.1512A>G (p.Ile504Met)
ClinVar dbSNP COSMIC

Number of alleles fetched