| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.140753332_140753333insTTCACTGTAGCTAGACCATCGAGA | CA891842051 | BRAF | c.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) | |
| 7 | g.140753338_140753355dup | CA645544101 | BRAF | c.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 |
| 7 | g.140753339_140753353del | CA891842052 | BRAF | c.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) | |
| 7 | g.140753339_140753340insTAGCTAGACCAAAATCACCTATTTTTT | CA645544107 | BRAF | c.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 |
| 7 | g.140753345_140753346delinsGA | CA16602421 | BRAF | c.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 |
| 7 | g.140753345_140753347dup | CA891842034 | BRAF | c.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) | |
| 7 | g.140753346G>A | CA168047474 | BRAF | c.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 |
| 7 | g.140753346G>C | CA123651 | BRAF | c.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 |
| 7 | g.140753346G>T | CA369543117 | BRAF | c.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) | |
| 7 | g.140753347A>C | CA457986988 | BRAF | c.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=) | |
| 7 | g.140753347A>G | CA457986990 | BRAF | c.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=) | |
| 7 | g.140753347A>T | CA457986991 | BRAF | c.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=) | |
| 7 | g.140753348C>A | CA220161 | BRAF | c.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 |
| 7 | g.140753348C>G | CA369543122 | BRAF | c.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) | |
| 7 | g.140753348C>T | CA16602814 | BRAF | c.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 |
| 7 | g.140753348del | CA457986993 | BRAF | c.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 |
| 7 | g.140753349C>A | CA135098 | BRAF | c.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 |
| 7 | g.140753349C>G | CA16602422 | BRAF | c.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 |
| 7 | g.140753349C>T | CA16602813 | BRAF | c.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 |
| 7 | g.140753350A>C | CA280058 | BRAF | c.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 |
| 7 | g.140753350A>G | CA457986995 | BRAF | c.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=) | |
| 7 | g.140753350A>T | CA295915 | BRAF | c.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 |
| 7 | g.140753351A>C | CA369543137 | BRAF | c.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) | |
| 7 | g.140753351A>G | CA16602738 | BRAF | c.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 |
| 7 | g.140753351A>T | CA369543141 | BRAF | c.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) | |
| 7 | g.140753352A>C | CA369543142 | BRAF | c.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) | |
| 7 | g.140753352A>G | CA280071 | BRAF | c.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 |
| 7 | g.140753352A>T | CA369543144 | BRAF | c.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) | |
| 7 | g.140753353A>C | CA16602423 | BRAF | c.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 |
| 7 | g.140753353A>G | CA457987004 | BRAF | c.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 |
| 7 | g.140753353A>T | CA16602424 | BRAF | c.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 |
| 7 | g.140753354T>A | CA16602425 | BRAF | c.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 |
| 7 | g.140753354T>C | CA123657 | BRAF | c.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 |
| 7 | g.140753354T>G | CA16602532 | BRAF | c.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 |
| 7 | g.140753354_140753357delinsCCAG | CA891842036 | BRAF | c.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) | |
| 7 | g.140753355C>A | CA369543156 | BRAF | c.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) | |
| 7 | g.140753355C>G | CA16602426 | BRAF | c.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 |
| 7 | g.140753355C>T | CA135095 | BRAF | c.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 |
| 7 | g.140753355_140753356delinsTC | CA16602427 | BRAF | c.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 |
| 7 | g.140753356A>C | CA457987011 | BRAF | c.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=) | |
| 7 | g.140753356A>G | CA457987012 | BRAF | c.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=) | |
| 7 | g.140753356A>T | CA457987013 | BRAF | c.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=) | |
| 7 | g.140753357C>A | CA369543160 | BRAF | c.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) | |
| 7 | g.140753357C>G | CA369543161 | BRAF | c.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) | |
| 7 | g.140753357C>T | CA369543163 | BRAF | c.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 |
| 7 | g.140753358C>A | CA369543165 | BRAF | c.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) | |
| 7 | g.140753358C>G | CA369543167 | BRAF | c.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) | |
| 7 | g.140753358C>T | CA369543170 | BRAF | c.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 |
| 7 | g.140753359T>A | CA457987019 | BRAF | c.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=) | |
| 7 | g.140753359T>C | CA16602739 | BRAF | c.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 |