| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 18 | g.53207664G>A | CA990384026 | DCC | c.1723-15G>A (n.1723-15G>A) c.1524-15G>A c.1654-15G>A (n.1654-15G>A) c.688-15G>A (n.688-15G>A) | dbSNP gnomAD v3 gnomAD v4 |
| 18 | g.53207664G= | CA2304037414 | DCC | c.1723-15G= (n.1723-15G=) c.1524-15G= c.1654-15G= (n.1654-15G=) c.688-15G= (n.688-15G=) | |
| 18 | g.53207665T>C | CA2641856297 | DCC | c.1723-14T>C (n.1723-14T>C) c.1524-14T>C c.1654-14T>C (n.1654-14T>C) c.688-14T>C (n.688-14T>C) | gnomAD v4 |
| 18 | g.53207665T>G | CA2641856298 | DCC | c.1723-14T>G (n.1723-14T>G) c.1524-14T>G c.1654-14T>G (n.1654-14T>G) c.688-14T>G (n.688-14T>G) | gnomAD v4 |
| 18 | g.53207666T>C | CA2812527172 | DCC | c.1723-13T>C (n.1723-13T>C) c.1524-13T>C c.1654-13T>C (n.1654-13T>C) c.688-13T>C (n.688-13T>C) | |
| 18 | g.53207667T>A | CA657081265 | DCC | c.1723-12T>A (n.1723-12T>A) c.1524-12T>A c.1654-12T>A (n.1654-12T>A) c.688-12T>A (n.688-12T>A) | COSMIC |
| 18 | g.53207668T>C | CA2641856299 | DCC | c.1723-11T>C (n.1723-11T>C) c.1524-11T>C c.1654-11T>C (n.1654-11T>C) c.688-11T>C (n.688-11T>C) | gnomAD v4 |
| 18 | g.53207669A= | CA2304037416 | DCC | c.1723-10A= (n.1723-10A=) c.1524-10A= c.1654-10A= (n.1654-10A=) c.688-10A= (n.688-10A=) | |
| 18 | g.53207669A>C | CA2641856300 | DCC | c.1723-10A>C (n.1723-10A>C) c.1524-10A>C c.1654-10A>C (n.1654-10A>C) c.688-10A>C (n.688-10A>C) | gnomAD v4 |
| 18 | g.53207669A>G | CA629976434 | DCC | c.1723-10A>G (n.1723-10A>G) c.1524-10A>G c.1654-10A>G (n.1654-10A>G) c.688-10A>G (n.688-10A>G) | dbSNP gnomAD v2 gnomAD v4 |
| 18 | g.53207670T>C | CA8966970 | DCC | c.1723-9T>C (n.1723-9T>C) c.1524-9T>C c.1654-9T>C (n.1654-9T>C) c.688-9T>C (n.688-9T>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.53207670T= | CA2304037419 | DCC | c.1723-9T= (n.1723-9T=) c.1524-9T= c.1654-9T= (n.1654-9T=) c.688-9T= (n.688-9T=) | |
| 18 | g.53207671G>A | CA780403507 | DCC | c.1723-8G>A (n.1723-8G>A) c.1524-8G>A c.1654-8G>A (n.1654-8G>A) c.688-8G>A (n.688-8G>A) | dbSNP gnomAD v3 gnomAD v4 |
| 18 | g.53207671G= | CA2304037421 | DCC | c.1723-8G= (n.1723-8G=) c.1524-8G= c.1654-8G= (n.1654-8G=) c.688-8G= (n.688-8G=) | |
| 18 | g.53207672T>C | CA2812527173 | DCC | c.1723-7T>C (n.1723-7T>C) c.1524-7T>C c.1654-7T>C (n.1654-7T>C) c.688-7T>C (n.688-7T>C) | |
| 18 | g.53207673C= | CA2304037422 | DCC | c.1723-6C= (n.1723-6C=) c.1524-6C= c.1654-6C= (n.1654-6C=) c.688-6C= (n.688-6C=) | |
| 18 | g.53207673C>G | CA8966971 | DCC | c.1723-6C>G (n.1723-6C>G) c.1524-6C>G c.1654-6C>G (n.1654-6C>G) c.688-6C>G (n.688-6C>G) | dbSNP ExAC gnomAD v3 gnomAD v4 |
| 18 | g.53207673C>T | CA2641856302 | DCC | c.1723-6C>T (n.1723-6C>T) c.1524-6C>T c.1654-6C>T (n.1654-6C>T) c.688-6C>T (n.688-6C>T) | gnomAD v4 |
| 18 | g.53207674_53207676dup | CA2641856301 | DCC | c.1723-5_1723-3dup (n.1723-5_1723-3dup) c.1524-5_1524-3dup c.1654-5_1654-3dup (n.1654-5_1654-3dup) c.688-5_688-3dup (n.688-5_688-3dup) | gnomAD v4 |
| 18 | g.53207674T>C | CA8966972 | DCC | c.1723-5T>C (n.1723-5T>C) c.1524-5T>C c.1654-5T>C (n.1654-5T>C) c.688-5T>C (n.688-5T>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.53207674T>G | CA629976435 | DCC | c.1723-5T>G (n.1723-5T>G) c.1524-5T>G c.1654-5T>G (n.1654-5T>G) c.688-5T>G (n.688-5T>G) | dbSNP gnomAD v2 |
| 18 | g.53207674T= | CA2304037427 | DCC | c.1723-5T= (n.1723-5T=) c.1524-5T= c.1654-5T= (n.1654-5T=) c.688-5T= (n.688-5T=) | |
| 18 | g.53207675C= | CA2304037430 | DCC | c.1723-4C= (n.1723-4C=) c.1524-4C= c.1654-4C= (n.1654-4C=) c.688-4C= (n.688-4C=) | |
| 18 | g.53207675C>T | CA8966973 | DCC | c.1723-4C>T (n.1723-4C>T) c.1524-4C>T c.1654-4C>T (n.1654-4C>T) c.688-4C>T (n.688-4C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.53207676C= | CA2304037433 | DCC | c.1723-3C= (n.1723-3C=) c.1524-3C= c.1654-3C= (n.1654-3C=) c.688-3C= (n.688-3C=) | |
| 18 | g.53207676C>T | CA2304037434 | DCC | c.1723-3C>T (n.1723-3C>T) c.1524-3C>T c.1654-3C>T (n.1654-3C>T) c.688-3C>T (n.688-3C>T) | dbSNP |
| 18 | g.53207677A>C | CA402518047 | DCC | c.1723-2A>C (n.1723-2A>C) c.1524-2A>C c.1654-2A>C (n.1654-2A>C) c.688-2A>C (n.688-2A>C) | |
| 18 | g.53207677A>G | CA402518048 | DCC | c.1723-2A>G (n.1723-2A>G) c.1524-2A>G c.1654-2A>G (n.1654-2A>G) c.688-2A>G (n.688-2A>G) | COSMIC COSMIC |
| 18 | g.53207677A>T | CA402518049 | DCC | c.1723-2A>T (n.1723-2A>T) c.1524-2A>T c.1654-2A>T (n.1654-2A>T) c.688-2A>T (n.688-2A>T) | |
| 18 | g.53207678G>A | CA402518050 | DCC | c.1723-1G>A (n.1723-1G>A) c.1524-1G>A c.1654-1G>A (n.1654-1G>A) c.688-1G>A (n.688-1G>A) | |
| 18 | g.53207678G>C | CA402518051 | DCC | c.1723-1G>C (n.1723-1G>C) c.1524-1G>C c.1654-1G>C (n.1654-1G>C) c.688-1G>C (n.688-1G>C) | |
| 18 | g.53207678G>T | CA402518052 | DCC | c.1723-1G>T (n.1723-1G>T) c.1524-1G>T c.1654-1G>T (n.1654-1G>T) c.688-1G>T (n.688-1G>T) | |
| 18 | g.53207679A>C | CA402518053 | DCC | c.1723A>C (p.Asn575His) c.1524A>C c.1654A>C (p.Asn552His) c.688A>C (p.Asn230His) | |
| 18 | g.53207679A>G | CA402518054 | DCC | c.1723A>G (p.Asn575Asp) c.1524A>G c.1654A>G (p.Asn552Asp) c.688A>G (p.Asn230Asp) | |
| 18 | g.53207679A>T | CA402518055 | DCC | c.1723A>T (p.Asn575Tyr) c.1524A>T c.1654A>T (p.Asn552Tyr) c.688A>T (p.Asn230Tyr) | |
| 18 | g.53207680A>C | CA402518056 | DCC | c.1724A>C (p.Asn575Thr) c.1525A>C c.1655A>C (p.Asn552Thr) c.689A>C (p.Asn230Thr) | |
| 18 | g.53207680A>G | CA402518058 | DCC | c.1724A>G (p.Asn575Ser) c.1525A>G c.1655A>G (p.Asn552Ser) c.689A>G (p.Asn230Ser) | |
| 18 | g.53207680A>T | CA402518057 | DCC | c.1724A>T (p.Asn575Ile) c.1525A>T c.1655A>T (p.Asn552Ile) c.689A>T (p.Asn230Ile) | |
| 18 | g.53207681T>A | CA402518059 | DCC | c.1725T>A (p.Asn575Lys) c.1526T>A c.1656T>A (p.Asn552Lys) c.690T>A (p.Asn230Lys) | |
| 18 | g.53207681T>C | CA503971834 | DCC | c.1725T>C (p.Asn575=) c.1526T>C c.1656T>C (p.Asn552=) c.690T>C (p.Asn230=) | dbSNP gnomAD v3 gnomAD v4 |
| 18 | g.53207681T>G | CA402518060 | DCC | c.1725T>G (p.Asn575Lys) c.1526T>G c.1656T>G (p.Asn552Lys) c.690T>G (p.Asn230Lys) | |
| 18 | g.53207681T= | CA2304037438 | DCC | c.1725T= (p.Asn575=) c.1526T= c.1656T= (p.Asn552=) c.690T= (p.Asn230=) | |
| 18 | g.53207682A= | CA2304037441 | DCC | c.1726A= (p.Ile576=) c.1527A= c.1657A= (p.Ile553=) c.691A= (p.Ile231=) | |
| 18 | g.53207682A>C | CA402518061 | DCC | c.1726A>C (p.Ile576Leu) c.1527A>C c.1657A>C (p.Ile553Leu) c.691A>C (p.Ile231Leu) | |
| 18 | g.53207682A>G | CA8966974 | DCC | c.1726A>G (p.Ile576Val) c.1527A>G c.1657A>G (p.Ile553Val) c.691A>G (p.Ile231Val) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.53207682A>T | CA402518062 | DCC | c.1726A>T (p.Ile576Leu) c.1527A>T c.1657A>T (p.Ile553Leu) c.691A>T (p.Ile231Leu) | gnomAD v4 |
| 18 | g.53207683T>A | CA402518063 | DCC | c.1727T>A (p.Ile576Lys) c.1528T>A c.1658T>A (p.Ile553Lys) c.692T>A (p.Ile231Lys) | |
| 18 | g.53207683T>C | CA8966975 | DCC | c.1727T>C (p.Ile576Thr) c.1528T>C c.1658T>C (p.Ile553Thr) c.692T>C (p.Ile231Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 18 | g.53207683T>G | CA402518064 | DCC | c.1727T>G (p.Ile576Arg) c.1528T>G c.1658T>G (p.Ile553Arg) c.692T>G (p.Ile231Arg) | |
| 18 | g.53207683T= | CA2304037446 | DCC | c.1727T= (p.Ile576=) c.1528T= c.1658T= (p.Ile553=) c.692T= (p.Ile231=) | |
| 18 | g.53207684A>C | CA503971835 | DCC | c.1728A>C (p.Ile576=) c.1529A>C c.1659A>C (p.Ile553=) c.693A>C (p.Ile231=) | |
| 18 | g.53207684A>G | CA402518065 | DCC | c.1728A>G (p.Ile576Met) c.1529A>G c.1659A>G (p.Ile553Met) c.693A>G (p.Ile231Met) | |
| 18 | g.53207684A>T | CA503971836 | DCC | c.1728A>T (p.Ile576=) c.1529A>T c.1659A>T (p.Ile553=) c.693A>T (p.Ile231=) | |
| 18 | g.53207685del | CA2695227774 | DCC | c.1729del (p.Glu577ArgfsTer12) c.1530del c.1660del (p.Glu554ArgfsTer12) c.694del (p.Glu232ArgfsTer12) | |
| 18 | g.53207685G>A | CA402518066 | DCC | c.1729G>A (p.Glu577Lys) c.1530G>A c.1660G>A (p.Glu554Lys) c.694G>A (p.Glu232Lys) | dbSNP gnomAD v3 gnomAD v4 |
| 18 | g.53207685G>C | CA300765513 | DCC | c.1729G>C (p.Glu577Gln) c.1530G>C c.1660G>C (p.Glu554Gln) c.694G>C (p.Glu232Gln) | dbSNP |
| 18 | g.53207685G= | CA2304037449 | DCC | c.1729G= (p.Glu577=) c.1530G= c.1660G= (p.Glu554=) c.694G= (p.Glu232=) | |
| 18 | g.53207685G>T | CA402518067 | DCC | c.1729G>T (p.Glu577Ter) c.1530G>T c.1660G>T (p.Glu554Ter) c.694G>T (p.Glu232Ter) | |
| 18 | g.53207686A>C | CA402518070 | DCC | c.1730A>C (p.Glu577Ala) c.1531A>C c.1661A>C (p.Glu554Ala) c.695A>C (p.Glu232Ala) | |
| 18 | g.53207686A>G | CA402518068 | DCC | c.1730A>G (p.Glu577Gly) c.1531A>G c.1661A>G (p.Glu554Gly) c.695A>G (p.Glu232Gly) | gnomAD v4 |
| 18 | g.53207686A>T | CA402518069 | DCC | c.1730A>T (p.Glu577Val) c.1531A>T c.1661A>T (p.Glu554Val) c.695A>T (p.Glu232Val) | |
| 18 | g.53207687G>A | CA503971838 | DCC | c.1731G>A (p.Glu577=) c.1532G>A c.1662G>A (p.Glu554=) c.696G>A (p.Glu232=) | |
| 18 | g.53207687G>C | CA402518071 | DCC | c.1731G>C (p.Glu577Asp) c.1532G>C c.1662G>C (p.Glu554Asp) c.696G>C (p.Glu232Asp) | |
| 18 | g.53207687G>T | CA402518072 | DCC | c.1731G>T (p.Glu577Asp) c.1532G>T c.1662G>T (p.Glu554Asp) c.696G>T (p.Glu232Asp) | |
| 18 | g.53207688G>A | CA402518073 | DCC | c.1732G>A (p.Val578Ile) c.1533G>A c.1663G>A (p.Val555Ile) c.697G>A (p.Val233Ile) | dbSNP gnomAD v4 |
| 18 | g.53207688G>C | CA402518074 | DCC | c.1732G>C (p.Val578Leu) c.1533G>C c.1663G>C (p.Val555Leu) c.697G>C (p.Val233Leu) | gnomAD v4 |
| 18 | g.53207688G= | CA2304037457 | DCC | c.1732G= (p.Val578=) c.1533G= c.1663G= (p.Val555=) c.697G= (p.Val233=) | |
| 18 | g.53207688G>T | CA402518075 | DCC | c.1732G>T (p.Val578Phe) c.1533G>T c.1663G>T (p.Val555Phe) c.697G>T (p.Val233Phe) | dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 18 | g.53207689T>A | CA402518076 | DCC | c.1733T>A (p.Val578Asp) c.1534T>A c.1664T>A (p.Val555Asp) c.698T>A (p.Val233Asp) | |
| 18 | g.53207689T>C | CA402518077 | DCC | c.1733T>C (p.Val578Ala) c.1534T>C c.1664T>C (p.Val555Ala) c.698T>C (p.Val233Ala) | dbSNP gnomAD v3 gnomAD v4 |
| 18 | g.53207689T>G | CA402518078 | DCC | c.1733T>G (p.Val578Gly) c.1534T>G c.1664T>G (p.Val555Gly) c.698T>G (p.Val233Gly) | |
| 18 | g.53207689T= | CA2304037459 | DCC | c.1733T= (p.Val578=) c.1534T= c.1664T= (p.Val555=) c.698T= (p.Val233=) | |
| 18 | g.53207690T>A | CA503971839 | DCC | c.1734T>A (p.Val578=) c.1535T>A c.1665T>A (p.Val555=) c.699T>A (p.Val233=) | |
| 18 | g.53207690T>C | CA503971840 | DCC | c.1734T>C (p.Val578=) c.1535T>C c.1665T>C (p.Val555=) c.699T>C (p.Val233=) | dbSNP |
| 18 | g.53207690T>G | CA503971841 | DCC | c.1734T>G (p.Val578=) c.1535T>G c.1665T>G (p.Val555=) c.699T>G (p.Val233=) | |
| 18 | g.53207690T= | CA2304037461 | DCC | c.1734T= (p.Val578=) c.1535T= c.1665T= (p.Val555=) c.699T= (p.Val233=) | |
| 18 | g.53207691G>A | CA8966976 | DCC | c.1735G>A (p.Asp579Asn) c.1536G>A c.1666G>A (p.Asp556Asn) c.700G>A (p.Asp234Asn) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.53207691G>C | CA402518079 | DCC | c.1735G>C (p.Asp579His) c.1536G>C c.1666G>C (p.Asp556His) c.700G>C (p.Asp234His) | |
| 18 | g.53207691G= | CA2304037464 | DCC | c.1735G= (p.Asp579=) c.1536G= c.1666G= (p.Asp556=) c.700G= (p.Asp234=) | |
| 18 | g.53207691G>T | CA402518080 | DCC | c.1735G>T (p.Asp579Tyr) c.1536G>T c.1666G>T (p.Asp556Tyr) c.700G>T (p.Asp234Tyr) | gnomAD v4 COSMIC COSMIC |
| 18 | g.53207692A= | CA2304037466 | DCC | c.1736A= (p.Asp579=) c.1537A= c.1667A= (p.Asp556=) c.701A= (p.Asp234=) | |
| 18 | g.53207692A>C | CA402518082 | DCC | c.1736A>C (p.Asp579Ala) c.1537A>C c.1667A>C (p.Asp556Ala) c.701A>C (p.Asp234Ala) | |
| 18 | g.53207692A>G | CA402518083 | DCC | c.1736A>G (p.Asp579Gly) c.1537A>G c.1667A>G (p.Asp556Gly) c.701A>G (p.Asp234Gly) | dbSNP gnomAD v3 gnomAD v4 |
| 18 | g.53207692A>T | CA402518081 | DCC | c.1736A>T (p.Asp579Val) c.1537A>T c.1667A>T (p.Asp556Val) c.701A>T (p.Asp234Val) | |
| 18 | g.53207693T>A | CA402518085 | DCC | c.1737T>A (p.Asp579Glu) c.1538T>A c.1668T>A (p.Asp556Glu) c.702T>A (p.Asp234Glu) | |
| 18 | g.53207693T>C | CA503971842 | DCC | c.1737T>C (p.Asp579=) c.1538T>C c.1668T>C (p.Asp556=) c.702T>C (p.Asp234=) | |
| 18 | g.53207693T>G | CA402518084 | DCC | c.1737T>G (p.Asp579Glu) c.1538T>G c.1668T>G (p.Asp556Glu) c.702T>G (p.Asp234Glu) | |
| 18 | g.53207694G>A | CA402518086 | DCC | c.1738G>A (p.Gly580Arg) c.1539G>A c.1669G>A (p.Gly557Arg) c.703G>A (p.Gly235Arg) | COSMIC |
| 18 | g.53207694G>C | CA402518087 | DCC | c.1738G>C (p.Gly580Arg) c.1539G>C c.1669G>C (p.Gly557Arg) c.703G>C (p.Gly235Arg) | |
| 18 | g.53207694G>T | CA402518088 | DCC | c.1738G>T (p.Gly580Ter) c.1539G>T c.1669G>T (p.Gly557Ter) c.703G>T (p.Gly235Ter) | |
| 18 | g.53207695G>A | CA402518089 | DCC | c.1739G>A (p.Gly580Glu) c.1540G>A c.1670G>A (p.Gly557Glu) c.704G>A (p.Gly235Glu) | gnomAD v4 |
| 18 | g.53207695G>C | CA402518090 | DCC | c.1739G>C (p.Gly580Ala) c.1540G>C c.1670G>C (p.Gly557Ala) c.704G>C (p.Gly235Ala) | |
| 18 | g.53207695G>T | CA402518091 | DCC | c.1739G>T (p.Gly580Val) c.1540G>T c.1670G>T (p.Gly557Val) c.704G>T (p.Gly235Val) | |
| 18 | g.53207696A= | CA2304037469 | DCC | c.1740A= (p.Gly580=) c.1541A= c.1671A= (p.Gly557=) c.705A= (p.Gly235=) | |
| 18 | g.53207696A>C | CA503971845 | DCC | c.1740A>C (p.Gly580=) c.1541A>C c.1671A>C (p.Gly557=) c.705A>C (p.Gly235=) | dbSNP |
| 18 | g.53207696A>G | CA503971843 | DCC | c.1740A>G (p.Gly580=) c.1541A>G c.1671A>G (p.Gly557=) c.705A>G (p.Gly235=) | |
| 18 | g.53207696A>T | CA503971844 | DCC | c.1740A>T (p.Gly580=) c.1541A>T c.1671A>T (p.Gly557=) c.705A>T (p.Gly235=) | |
| 18 | g.53207697C>A | CA402518092 | DCC | c.1741C>A (p.Leu581Ile) c.1542C>A c.1672C>A (p.Leu558Ile) c.706C>A (p.Leu236Ile) | |
| 18 | g.53207697C>G | CA402518093 | DCC | c.1741C>G (p.Leu581Val) c.1542C>G c.1672C>G (p.Leu558Val) c.706C>G (p.Leu236Val) | |
| 18 | g.53207697C>T | CA503971846 | DCC | c.1741C>T (p.Leu581=) c.1542C>T c.1672C>T (p.Leu558=) c.706C>T (p.Leu236=) | |
| 18 | g.53207698T>A | CA402518094 | DCC | c.1742T>A (p.Leu581Gln) c.1543T>A c.1673T>A (p.Leu558Gln) c.707T>A (p.Leu236Gln) | |
| 18 | g.53207698T>C | CA402518095 | DCC | c.1742T>C (p.Leu581Pro) c.1543T>C c.1673T>C (p.Leu558Pro) c.707T>C (p.Leu236Pro) | |
| 18 | g.53207698T>G | CA402518096 | DCC | c.1742T>G (p.Leu581Arg) c.1543T>G c.1673T>G (p.Leu558Arg) c.707T>G (p.Leu236Arg) | |
| 18 | g.53207699A= | CA2304037473 | DCC | c.1743A= (p.Leu581=) c.1544A= c.1674A= (p.Leu558=) c.708A= (p.Leu236=) | |
| 18 | g.53207699A>C | CA503971847 | DCC | c.1743A>C (p.Leu581=) c.1544A>C c.1674A>C (p.Leu558=) c.708A>C (p.Leu236=) | |
| 18 | g.53207699A>G | CA8966977 | DCC | c.1743A>G (p.Leu581=) c.1544A>G c.1674A>G (p.Leu558=) c.708A>G (p.Leu236=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.53207699A>T | CA503971848 | DCC | c.1743A>T (p.Leu581=) c.1544A>T c.1674A>T (p.Leu558=) c.708A>T (p.Leu236=) | |
| 18 | g.53207700T>A | CA402518097 | DCC | c.1744T>A (p.Ser582Thr) c.1545T>A c.1675T>A (p.Ser559Thr) c.709T>A (p.Ser237Thr) | |
| 18 | g.53207700T>C | CA300765514 | DCC | c.1744T>C (p.Ser582Pro) c.1545T>C c.1675T>C (p.Ser559Pro) c.709T>C (p.Ser237Pro) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.53207700T>G | CA402518098 | DCC | c.1744T>G (p.Ser582Ala) c.1545T>G c.1675T>G (p.Ser559Ala) c.709T>G (p.Ser237Ala) | gnomAD v4 |
| 18 | g.53207700T= | CA2304037475 | DCC | c.1744T= (p.Ser582=) c.1545T= c.1675T= (p.Ser559=) c.709T= (p.Ser237=) | |
| 18 | g.53207701C>A | CA402518099 | DCC | c.1745C>A (p.Ser582Tyr) c.1546C>A c.1676C>A (p.Ser559Tyr) c.710C>A (p.Ser237Tyr) | |
| 18 | g.53207701C= | CA2304037480 | DCC | c.1745C= (p.Ser582=) c.1546C= c.1676C= (p.Ser559=) c.710C= (p.Ser237=) | |
| 18 | g.53207701C>G | CA402518100 | DCC | c.1745C>G (p.Ser582Cys) c.1546C>G c.1676C>G (p.Ser559Cys) c.710C>G (p.Ser237Cys) | |
| 18 | g.53207701C>T | CA402518101 | DCC | c.1745C>T (p.Ser582Phe) c.1546C>T c.1676C>T (p.Ser559Phe) c.710C>T (p.Ser237Phe) | dbSNP gnomAD v4 COSMIC COSMIC |
| 18 | g.53207702T>A | CA503971849 | DCC | c.1746T>A (p.Ser582=) c.1547T>A c.1677T>A (p.Ser559=) c.711T>A (p.Ser237=) | |
| 18 | g.53207702T>C | CA503971851 | DCC | c.1746T>C (p.Ser582=) c.1547T>C c.1677T>C (p.Ser559=) c.711T>C (p.Ser237=) | |
| 18 | g.53207702T>G | CA503971850 | DCC | c.1746T>G (p.Ser582=) c.1547T>G c.1677T>G (p.Ser559=) c.711T>G (p.Ser237=) | |
| 18 | g.53207703T>A | CA402518102 | DCC | c.1747T>A (p.Tyr583Asn) c.1548T>A c.1678T>A (p.Tyr560Asn) c.712T>A (p.Tyr238Asn) | |
| 18 | g.53207703T>C | CA402518103 | DCC | c.1747T>C (p.Tyr583His) c.1548T>C c.1678T>C (p.Tyr560His) c.712T>C (p.Tyr238His) | gnomAD v4 |
| 18 | g.53207703T>G | CA402518104 | DCC | c.1747T>G (p.Tyr583Asp) c.1548T>G c.1678T>G (p.Tyr560Asp) c.712T>G (p.Tyr238Asp) | |
| 18 | g.53207704A= | CA2304037484 | DCC | c.1748A= (p.Tyr583=) c.1549A= c.1679A= (p.Tyr560=) c.713A= (p.Tyr238=) | |
| 18 | g.53207704A>C | CA402518105 | DCC | c.1748A>C (p.Tyr583Ser) c.1549A>C c.1679A>C (p.Tyr560Ser) c.713A>C (p.Tyr238Ser) | |
| 18 | g.53207704A>G | CA300765515 | DCC | c.1748A>G (p.Tyr583Cys) c.1549A>G c.1679A>G (p.Tyr560Cys) c.713A>G (p.Tyr238Cys) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.53207704A>T | CA402518106 | DCC | c.1748A>T (p.Tyr583Phe) c.1549A>T c.1679A>T (p.Tyr560Phe) c.713A>T (p.Tyr238Phe) | |
| 18 | g.53207705T>A | CA402518107 | DCC | c.1749T>A (p.Tyr583Ter) c.1550T>A c.1680T>A (p.Tyr560Ter) c.714T>A (p.Tyr238Ter) | |
| 18 | g.53207705T>C | CA503971852 | DCC | c.1749T>C (p.Tyr583=) c.1550T>C c.1680T>C (p.Tyr560=) c.714T>C (p.Tyr238=) | dbSNP gnomAD v4 |
| 18 | g.53207705T>G | CA402518108 | DCC | c.1749T>G (p.Tyr583Ter) c.1550T>G c.1680T>G (p.Tyr560Ter) c.714T>G (p.Tyr238Ter) | |
| 18 | g.53207705T= | CA2304037485 | DCC | c.1749T= (p.Tyr583=) c.1550T= c.1680T= (p.Tyr560=) c.714T= (p.Tyr238=) | |
| 18 | g.53207706A>C | CA402518110 | DCC | c.1750A>C (p.Lys584Gln) c.1551A>C c.1681A>C (p.Lys561Gln) c.715A>C (p.Lys239Gln) | |
| 18 | g.53207706A>G | CA402518111 | DCC | c.1750A>G (p.Lys584Glu) c.1551A>G c.1681A>G (p.Lys561Glu) c.715A>G (p.Lys239Glu) | gnomAD v4 COSMIC COSMIC |
| 18 | g.53207706A>T | CA402518109 | DCC | c.1750A>T (p.Lys584Ter) c.1551A>T c.1681A>T (p.Lys561Ter) c.715A>T (p.Lys239Ter) | |
| 18 | g.53207707A= | CA2304037486 | DCC | c.1751A= (p.Lys584=) c.1552A= c.1682A= (p.Lys561=) c.716A= (p.Lys239=) | |
| 18 | g.53207707A>C | CA300765516 | DCC | c.1751A>C (p.Lys584Thr) c.1552A>C c.1682A>C (p.Lys561Thr) c.716A>C (p.Lys239Thr) | dbSNP gnomAD v3 gnomAD v4 |
| 18 | g.53207707A>G | CA402518112 | DCC | c.1751A>G (p.Lys584Arg) c.1552A>G c.1682A>G (p.Lys561Arg) c.716A>G (p.Lys239Arg) | |
| 18 | g.53207707A>T | CA402518113 | DCC | c.1751A>T (p.Lys584Ile) c.1552A>T c.1682A>T (p.Lys561Ile) c.716A>T (p.Lys239Ile) | |
| 18 | g.53207708A>C | CA402518114 | DCC | c.1752A>C (p.Lys584Asn) c.1553A>C c.1683A>C (p.Lys561Asn) c.717A>C (p.Lys239Asn) | |
| 18 | g.53207708A>G | CA503971853 | DCC | c.1752A>G (p.Lys584=) c.1553A>G c.1683A>G (p.Lys561=) c.717A>G (p.Lys239=) | |
| 18 | g.53207708A>T | CA402518115 | DCC | c.1752A>T (p.Lys584Asn) c.1553A>T c.1683A>T (p.Lys561Asn) c.717A>T (p.Lys239Asn) | |
| 18 | g.53207709C>A | CA402518116 | DCC | c.1753C>A (p.Leu585Met) c.1554C>A c.1684C>A (p.Leu562Met) c.718C>A (p.Leu240Met) | gnomAD v4 |
| 18 | g.53207709C>G | CA402518117 | DCC | c.1753C>G (p.Leu585Val) c.1554C>G c.1684C>G (p.Leu562Val) c.718C>G (p.Leu240Val) | |
| 18 | g.53207709C>T | CA503971854 | DCC | c.1753C>T (p.Leu585=) c.1554C>T c.1684C>T (p.Leu562=) c.718C>T (p.Leu240=) | gnomAD v4 |
| 18 | g.53207710T>A | CA402518118 | DCC | c.1754T>A (p.Leu585Gln) c.1555T>A c.1685T>A (p.Leu562Gln) c.719T>A (p.Leu240Gln) | |
| 18 | g.53207710T>C | CA402518119 | DCC | c.1754T>C (p.Leu585Pro) c.1555T>C c.1685T>C (p.Leu562Pro) c.719T>C (p.Leu240Pro) | |
| 18 | g.53207710T>G | CA402518120 | DCC | c.1754T>G (p.Leu585Arg) c.1555T>G c.1685T>G (p.Leu562Arg) c.719T>G (p.Leu240Arg) | |
| 18 | g.53207711G>A | CA503971855 | DCC | c.1755G>A (p.Leu585=) c.1556G>A c.1686G>A (p.Leu562=) c.720G>A (p.Leu240=) | dbSNP gnomAD v4 |
| 18 | g.53207711G>C | CA503971856 | DCC | c.1755G>C (p.Leu585=) c.1556G>C c.1686G>C (p.Leu562=) c.720G>C (p.Leu240=) | |
| 18 | g.53207711G= | CA2304037489 | DCC | c.1755G= (p.Leu585=) c.1556G= c.1686G= (p.Leu562=) c.720G= (p.Leu240=) | |
| 18 | g.53207711G>T | CA503971857 | DCC | c.1755G>T (p.Leu585=) c.1556G>T c.1686G>T (p.Leu562=) c.720G>T (p.Leu240=) | |
| 18 | g.53207712G>A | CA402518121 | DCC | c.1756G>A (p.Glu586Lys) c.1557G>A c.1687G>A (p.Glu563Lys) c.721G>A (p.Glu241Lys) | COSMIC COSMIC |
| 18 | g.53207712G>C | CA402518122 | DCC | c.1756G>C (p.Glu586Gln) c.1557G>C c.1687G>C (p.Glu563Gln) c.721G>C (p.Glu241Gln) | dbSNP gnomAD v4 |
| 18 | g.53207712G>T | CA402518123 | DCC | c.1756G>T (p.Glu586Ter) c.1557G>T c.1687G>T (p.Glu563Ter) c.721G>T (p.Glu241Ter) | |
| 18 | g.53207713A>C | CA402518126 | DCC | c.1757A>C (p.Glu586Ala) c.1558A>C c.1688A>C (p.Glu563Ala) c.722A>C (p.Glu241Ala) | |
| 18 | g.53207713A>G | CA402518125 | DCC | c.1757A>G (p.Glu586Gly) c.1558A>G c.1688A>G (p.Glu563Gly) c.722A>G (p.Glu241Gly) | |
| 18 | g.53207713A>T | CA402518124 | DCC | c.1757A>T (p.Glu586Val) c.1558A>T c.1688A>T (p.Glu563Val) c.722A>T (p.Glu241Val) | |
| 18 | g.53207714A= | CA2304037491 | DCC | c.1758A= (p.Glu586=) c.1559A= c.1689A= (p.Glu563=) c.723A= (p.Glu241=) | |
| 18 | g.53207714A>C | CA402518127 | DCC | c.1758A>C (p.Glu586Asp) c.1559A>C c.1689A>C (p.Glu563Asp) c.723A>C (p.Glu241Asp) | |
| 18 | g.53207714A>G | CA503971858 | DCC | c.1758A>G (p.Glu586=) c.1559A>G c.1689A>G (p.Glu563=) c.723A>G (p.Glu241=) | dbSNP |
| 18 | g.53207714A>T | CA402518128 | DCC | c.1758A>T (p.Glu586Asp) c.1559A>T c.1689A>T (p.Glu563Asp) c.723A>T (p.Glu241Asp) | |
| 18 | g.53207715G>A | CA402518129 | DCC | c.1759G>A (p.Gly587Ser) c.1560G>A c.1690G>A (p.Gly564Ser) c.724G>A (p.Gly242Ser) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.53207715G>C | CA8966978 | DCC | c.1759G>C (p.Gly587Arg) c.1560G>C c.1690G>C (p.Gly564Arg) c.724G>C (p.Gly242Arg) | dbSNP ExAC gnomAD v2 |
| 18 | g.53207715G= | CA2304037492 | DCC | c.1759G= (p.Gly587=) c.1560G= c.1690G= (p.Gly564=) c.724G= (p.Gly242=) | |
| 18 | g.53207715G>T | CA402518130 | DCC | c.1759G>T (p.Gly587Cys) c.1560G>T c.1690G>T (p.Gly564Cys) c.724G>T (p.Gly242Cys) | |
| 18 | g.53207716G>A | CA402518131 | DCC | c.1760G>A (p.Gly587Asp) c.1561G>A c.1691G>A (p.Gly564Asp) c.725G>A (p.Gly242Asp) | dbSNP |
| 18 | g.53207716G>C | CA402518132 | DCC | c.1760G>C (p.Gly587Ala) c.1561G>C c.1691G>C (p.Gly564Ala) c.725G>C (p.Gly242Ala) | dbSNP gnomAD v2 gnomAD v4 |
| 18 | g.53207716G= | CA2304037493 | DCC | c.1760G= (p.Gly587=) c.1561G= c.1691G= (p.Gly564=) c.725G= (p.Gly242=) | |
| 18 | g.53207716G>T | CA8966979 | DCC | c.1760G>T (p.Gly587Val) c.1561G>T c.1691G>T (p.Gly564Val) c.725G>T (p.Gly242Val) | dbSNP ExAC gnomAD v2 |
| 18 | g.53207717C>A | CA503971861 | DCC | c.1761C>A (p.Gly587=) c.1562C>A c.1692C>A (p.Gly564=) c.726C>A (p.Gly242=) | |
| 18 | g.53207717C>G | CA503971859 | DCC | c.1761C>G (p.Gly587=) c.1562C>G c.1692C>G (p.Gly564=) c.726C>G (p.Gly242=) | |
| 18 | g.53207717C>T | CA503971860 | DCC | c.1761C>T (p.Gly587=) c.1562C>T c.1692C>T (p.Gly564=) c.726C>T (p.Gly242=) | gnomAD v4 |
| 18 | g.53207718C>A | CA402518133 | DCC | c.1762C>A (p.Leu588Met) c.1563C>A c.1693C>A (p.Leu565Met) c.727C>A (p.Leu243Met) | |
| 18 | g.53207718C>G | CA402518134 | DCC | c.1762C>G (p.Leu588Val) c.1563C>G c.1693C>G (p.Leu565Val) c.727C>G (p.Leu243Val) | |
| 18 | g.53207718C>T | CA503971862 | DCC | c.1762C>T (p.Leu588=) c.1563C>T c.1693C>T (p.Leu565=) c.727C>T (p.Leu243=) | |
| 18 | g.53207719T>A | CA402518135 | DCC | c.1763T>A (p.Leu588Gln) c.1564T>A c.1694T>A (p.Leu565Gln) c.728T>A (p.Leu243Gln) | |
| 18 | g.53207719T>C | CA402518136 | DCC | c.1763T>C (p.Leu588Pro) c.1564T>C c.1694T>C (p.Leu565Pro) c.728T>C (p.Leu243Pro) | COSMIC COSMIC |
| 18 | g.53207719T>G | CA402518137 | DCC | c.1763T>G (p.Leu588Arg) c.1564T>G c.1694T>G (p.Leu565Arg) c.728T>G (p.Leu243Arg) | |
| 18 | g.53207720G>A | CA503971863 | DCC | c.1764G>A (p.Leu588=) c.1565G>A c.1695G>A (p.Leu565=) c.729G>A (p.Leu243=) | COSMIC COSMIC |
| 18 | g.53207720G>C | CA503971864 | DCC | c.1764G>C (p.Leu588=) c.1565G>C c.1695G>C (p.Leu565=) c.729G>C (p.Leu243=) | dbSNP |
| 18 | g.53207720G>T | CA503971865 | DCC | c.1764G>T (p.Leu588=) c.1565G>T c.1695G>T (p.Leu565=) c.729G>T (p.Leu243=) | |
| 18 | g.53207721A>C | CA402518140 | DCC | c.1765A>C (p.Lys589Gln) c.1566A>C c.1696A>C (p.Lys566Gln) c.730A>C (p.Lys244Gln) | |
| 18 | g.53207721A>G | CA402518139 | DCC | c.1765A>G (p.Lys589Glu) c.1566A>G c.1696A>G (p.Lys566Glu) c.730A>G (p.Lys244Glu) | gnomAD v4 |
| 18 | g.53207721A>T | CA402518138 | DCC | c.1765A>T (p.Lys589Ter) c.1566A>T c.1696A>T (p.Lys566Ter) c.730A>T (p.Lys244Ter) | |
| 18 | g.53207726del | CA2735223461 | DCC | c.1770del (p.Lys590AsnfsTer10) c.1571del c.1701del (p.Lys567AsnfsTer10) c.735del (p.Lys245AsnfsTer10) | dbSNP |
| 18 | g.53207722A>C | CA402518141 | DCC | c.1766A>C (p.Lys589Thr) c.1567A>C c.1697A>C (p.Lys566Thr) c.731A>C (p.Lys244Thr) | |
| 18 | g.53207722A>G | CA402518143 | DCC | c.1766A>G (p.Lys589Arg) c.1567A>G c.1697A>G (p.Lys566Arg) c.731A>G (p.Lys244Arg) | |
| 18 | g.53207722A>T | CA402518142 | DCC | c.1766A>T (p.Lys589Ile) c.1567A>T c.1697A>T (p.Lys566Ile) c.731A>T (p.Lys244Ile) | gnomAD v4 |
| 18 | g.53207723A>C | CA402518144 | DCC | c.1767A>C (p.Lys589Asn) c.1568A>C c.1698A>C (p.Lys566Asn) c.732A>C (p.Lys244Asn) | COSMIC COSMIC |
| 18 | g.53207723A>G | CA503971866 | DCC | c.1767A>G (p.Lys589=) c.1568A>G c.1698A>G (p.Lys566=) c.732A>G (p.Lys244=) | |
| 18 | g.53207723A>T | CA402518145 | DCC | c.1767A>T (p.Lys589Asn) c.1568A>T c.1698A>T (p.Lys566Asn) c.732A>T (p.Lys244Asn) | |
| 18 | g.53207724A>C | CA402518146 | DCC | c.1768A>C (p.Lys590Gln) c.1569A>C c.1699A>C (p.Lys567Gln) c.733A>C (p.Lys245Gln) | |
| 18 | g.53207724A>G | CA402518147 | DCC | c.1768A>G (p.Lys590Glu) c.1569A>G c.1699A>G (p.Lys567Glu) c.733A>G (p.Lys245Glu) | |
| 18 | g.53207724A>T | CA402518148 | DCC | c.1768A>T (p.Lys590Ter) c.1569A>T c.1699A>T (p.Lys567Ter) c.733A>T (p.Lys245Ter) | |
| 18 | g.53207725A>C | CA402518149 | DCC | c.1769A>C (p.Lys590Thr) c.1570A>C c.1700A>C (p.Lys567Thr) c.734A>C (p.Lys245Thr) | |
| 18 | g.53207725A>G | CA402518150 | DCC | c.1769A>G (p.Lys590Arg) c.1570A>G c.1700A>G (p.Lys567Arg) c.734A>G (p.Lys245Arg) | |
| 18 | g.53207725A>T | CA402518151 | DCC | c.1769A>T (p.Lys590Ile) c.1570A>T c.1700A>T (p.Lys567Ile) c.734A>T (p.Lys245Ile) | COSMIC COSMIC |
| 18 | g.53207726A= | CA2304037494 | DCC | c.1770A= (p.Lys590=) c.1571A= c.1701A= (p.Lys567=) c.735A= (p.Lys245=) | |
| 18 | g.53207726A>C | CA402518152 | DCC | c.1770A>C (p.Lys590Asn) c.1571A>C c.1701A>C (p.Lys567Asn) c.735A>C (p.Lys245Asn) | |
| 18 | g.53207726A>G | CA503971867 | DCC | c.1770A>G (p.Lys590=) c.1571A>G c.1701A>G (p.Lys567=) c.735A>G (p.Lys245=) | dbSNP gnomAD v2 gnomAD v4 |
| 18 | g.53207726A>T | CA402518153 | DCC | c.1770A>T (p.Lys590Asn) c.1571A>T c.1701A>T (p.Lys567Asn) c.735A>T (p.Lys245Asn) | |
| 18 | g.53207727T>A | CA402518154 | DCC | c.1771T>A (p.Phe591Ile) c.1572T>A c.1702T>A (p.Phe568Ile) c.736T>A (p.Phe246Ile) | |
| 18 | g.53207727T>C | CA402518155 | DCC | c.1771T>C (p.Phe591Leu) c.1572T>C c.1702T>C (p.Phe568Leu) c.736T>C (p.Phe246Leu) | |
| 18 | g.53207727T>G | CA402518156 | DCC | c.1771T>G (p.Phe591Val) c.1572T>G c.1702T>G (p.Phe568Val) c.736T>G (p.Phe246Val) | |
| 18 | g.53207728T>A | CA402518159 | DCC | c.1772T>A (p.Phe591Tyr) c.1573T>A c.1703T>A (p.Phe568Tyr) c.737T>A (p.Phe246Tyr) | |
| 18 | g.53207728T>C | CA402518157 | DCC | c.1772T>C (p.Phe591Ser) c.1573T>C c.1703T>C (p.Phe568Ser) c.737T>C (p.Phe246Ser) | |
| 18 | g.53207728T>G | CA402518158 | DCC | c.1772T>G (p.Phe591Cys) c.1573T>G c.1703T>G (p.Phe568Cys) c.737T>G (p.Phe246Cys) | |
| 18 | g.53207729C>A | CA402518160 | DCC | c.1773C>A (p.Phe591Leu) c.1574C>A c.1704C>A (p.Phe568Leu) c.738C>A (p.Phe246Leu) | |
| 18 | g.53207729C>G | CA402518161 | DCC | c.1773C>G (p.Phe591Leu) c.1574C>G c.1704C>G (p.Phe568Leu) c.738C>G (p.Phe246Leu) | |
| 18 | g.53207729C>T | CA503971868 | DCC | c.1773C>T (p.Phe591=) c.1574C>T c.1704C>T (p.Phe568=) c.738C>T (p.Phe246=) | |
| 18 | g.53207730A= | CA2304037497 | DCC | c.1774A= (p.Thr592=) c.1575A= c.1705A= (p.Thr569=) c.739A= (p.Thr247=) | |
| 18 | g.53207730A>C | CA402518162 | DCC | c.1774A>C (p.Thr592Pro) c.1575A>C c.1705A>C (p.Thr569Pro) c.739A>C (p.Thr247Pro) | |
| 18 | g.53207730A>G | CA8966980 | DCC | c.1774A>G (p.Thr592Ala) c.1575A>G c.1705A>G (p.Thr569Ala) c.739A>G (p.Thr247Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.53207730A>T | CA8966981 | DCC | c.1774A>T (p.Thr592Ser) c.1575A>T c.1705A>T (p.Thr569Ser) c.739A>T (p.Thr247Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 18 | g.53207731C>A | CA402518163 | DCC | c.1775C>A (p.Thr592Asn) c.1576C>A c.1706C>A (p.Thr569Asn) c.740C>A (p.Thr247Asn) | |
| 18 | g.53207731C= | CA2304037498 | DCC | c.1775C= (p.Thr592=) c.1576C= c.1706C= (p.Thr569=) c.740C= (p.Thr247=) | |
| 18 | g.53207731C>G | CA402518164 | DCC | c.1775C>G (p.Thr592Ser) c.1576C>G c.1706C>G (p.Thr569Ser) c.740C>G (p.Thr247Ser) | |
| 18 | g.53207731C>T | CA300765517 | DCC | c.1775C>T (p.Thr592Ile) c.1576C>T c.1706C>T (p.Thr569Ile) c.740C>T (p.Thr247Ile) | dbSNP COSMIC COSMIC |
| 18 | g.53207732C>A | CA503971869 | DCC | c.1776C>A (p.Thr592=) c.1577C>A c.1707C>A (p.Thr569=) c.741C>A (p.Thr247=) | COSMIC |
| 18 | g.53207732C= | CA2304037500 | DCC | c.1776C= (p.Thr592=) c.1577C= c.1707C= (p.Thr569=) c.741C= (p.Thr247=) | |
| 18 | g.53207732C>G | CA503971870 | DCC | c.1776C>G (p.Thr592=) c.1577C>G c.1707C>G (p.Thr569=) c.741C>G (p.Thr247=) | |
| 18 | g.53207732C>T | CA300765518 | DCC | c.1776C>T (p.Thr592=) c.1577C>T c.1707C>T (p.Thr569=) c.741C>T (p.Thr247=) | dbSNP gnomAD v4 COSMIC COSMIC |
| 18 | g.53207733G>A | CA8966982 | DCC | c.1777G>A (p.Glu593Lys) c.1578G>A c.1708G>A (p.Glu570Lys) c.742G>A (p.Glu248Lys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.53207733G>C | CA402518165 | DCC | c.1777G>C (p.Glu593Gln) c.1578G>C c.1708G>C (p.Glu570Gln) c.742G>C (p.Glu248Gln) | |
| 18 | g.53207733G= | CA2304037502 | DCC | c.1777G= (p.Glu593=) c.1578G= c.1708G= (p.Glu570=) c.742G= (p.Glu248=) | |
| 18 | g.53207733G>T | CA402518166 | DCC | c.1777G>T (p.Glu593Ter) c.1578G>T c.1708G>T (p.Glu570Ter) c.742G>T (p.Glu248Ter) | gnomAD v4 |
| 18 | g.53207734A>C | CA402518168 | DCC | c.1778A>C (p.Glu593Ala) c.1579A>C c.1709A>C (p.Glu570Ala) c.743A>C (p.Glu248Ala) | |
| 18 | g.53207734A>G | CA402518169 | DCC | c.1778A>G (p.Glu593Gly) c.1579A>G c.1709A>G (p.Glu570Gly) c.743A>G (p.Glu248Gly) | |
| 18 | g.53207734A>T | CA402518167 | DCC | c.1778A>T (p.Glu593Val) c.1579A>T c.1709A>T (p.Glu570Val) c.743A>T (p.Glu248Val) | |
| 18 | g.53207735A= | CA2304037504 | DCC | c.1779A= (p.Glu593=) c.1580A= c.1710A= (p.Glu570=) c.744A= (p.Glu248=) | |
| 18 | g.53207735A>C | CA402518170 | DCC | c.1779A>C (p.Glu593Asp) c.1580A>C c.1710A>C (p.Glu570Asp) c.744A>C (p.Glu248Asp) | |
| 18 | g.53207735A>G | CA8966983 | DCC | c.1779A>G (p.Glu593=) c.1580A>G c.1710A>G (p.Glu570=) c.744A>G (p.Glu248=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 18 | g.53207735A>T | CA402518171 | DCC | c.1779A>T (p.Glu593Asp) c.1580A>T c.1710A>T (p.Glu570Asp) c.744A>T (p.Glu248Asp) | |
| 18 | g.53207735_53207736insCACACCCAACACA | CA2812527174 | DCC | c.1779_1780insCACACCCAACACA (p.Tyr594HisfsTer6) c.1580_1581insCACACCCAACACA c.1710_1711insCACACCCAACACA (p.Tyr571HisfsTer6) c.744_745insCACACCCAACACA (p.Tyr249HisfsTer6) | |
| 18 | g.53207736T>A | CA402518172 | DCC | c.1780T>A (p.Tyr594Asn) c.1581T>A c.1711T>A (p.Tyr571Asn) c.745T>A (p.Tyr249Asn) | |
| 18 | g.53207736T>C | CA402518173 | DCC | c.1780T>C (p.Tyr594His) c.1581T>C c.1711T>C (p.Tyr571His) c.745T>C (p.Tyr249His) | |
| 18 | g.53207736T>G | CA402518174 | DCC | c.1780T>G (p.Tyr594Asp) c.1581T>G c.1711T>G (p.Tyr571Asp) c.745T>G (p.Tyr249Asp) | dbSNP |
| 18 | g.53207736T= | CA2304037505 | DCC | c.1780T= (p.Tyr594=) c.1581T= c.1711T= (p.Tyr571=) c.745T= (p.Tyr249=) | |
| 18 | g.53207737A>C | CA402518175 | DCC | c.1781A>C (p.Tyr594Ser) c.1582A>C c.1712A>C (p.Tyr571Ser) c.746A>C (p.Tyr249Ser) | |
| 18 | g.53207737A>G | CA402518176 | DCC | c.1781A>G (p.Tyr594Cys) c.1582A>G c.1712A>G (p.Tyr571Cys) c.746A>G (p.Tyr249Cys) | |
| 18 | g.53207737A>T | CA402518177 | DCC | c.1781A>T (p.Tyr594Phe) c.1582A>T c.1712A>T (p.Tyr571Phe) c.746A>T (p.Tyr249Phe) | |
| 18 | g.53207738T>A | CA402518178 | DCC | c.1782T>A (p.Tyr594Ter) c.1583T>A c.1713T>A (p.Tyr571Ter) c.747T>A (p.Tyr249Ter) | COSMIC COSMIC |
| 18 | g.53207738T>C | CA503971871 | DCC | c.1782T>C (p.Tyr594=) c.1583T>C c.1713T>C (p.Tyr571=) c.747T>C (p.Tyr249=) | gnomAD v4 |
| 18 | g.53207738T>G | CA402518179 | DCC | c.1782T>G (p.Tyr594Ter) c.1583T>G c.1713T>G (p.Tyr571Ter) c.747T>G (p.Tyr249Ter) | |
| 18 | g.53207739A>C | CA402518181 | DCC | c.1783A>C (p.Ser595Arg) c.1584A>C c.1714A>C (p.Ser572Arg) c.748A>C (p.Ser250Arg) | |
| 18 | g.53207739A>G | CA402518182 | DCC | c.1783A>G (p.Ser595Gly) c.1584A>G c.1714A>G (p.Ser572Gly) c.748A>G (p.Ser250Gly) | |
| 18 | g.53207739A>T | CA402518180 | DCC | c.1783A>T (p.Ser595Cys) c.1584A>T c.1714A>T (p.Ser572Cys) c.748A>T (p.Ser250Cys) | |
| 18 | g.53207740G>A | CA402518183 | DCC | c.1784G>A (p.Ser595Asn) c.1585G>A c.1715G>A (p.Ser572Asn) c.749G>A (p.Ser250Asn) | COSMIC |
| 18 | g.53207740G>C | CA402518184 | DCC | c.1784G>C (p.Ser595Thr) c.1585G>C c.1715G>C (p.Ser572Thr) c.749G>C (p.Ser250Thr) | |
| 18 | g.53207740G= | CA2304037509 | DCC | c.1784G= (p.Ser595=) c.1585G= c.1715G= (p.Ser572=) c.749G= (p.Ser250=) | |
| 18 | g.53207740G>T | CA402518185 | DCC | c.1784G>T (p.Ser595Ile) c.1585G>T c.1715G>T (p.Ser572Ile) c.749G>T (p.Ser250Ile) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.53207741T>A | CA402518186 | DCC | c.1785T>A (p.Ser595Arg) c.1586T>A c.1716T>A (p.Ser572Arg) c.750T>A (p.Ser250Arg) | |
| 18 | g.53207741T>C | CA503971872 | DCC | c.1785T>C (p.Ser595=) c.1586T>C c.1716T>C (p.Ser572=) c.750T>C (p.Ser250=) | |
| 18 | g.53207741T>G | CA8966984 | DCC | c.1785T>G (p.Ser595Arg) c.1586T>G c.1716T>G (p.Ser572Arg) c.750T>G (p.Ser250Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 18 | g.53207741T= | CA2304037511 | DCC | c.1785T= (p.Ser595=) c.1586T= c.1716T= (p.Ser572=) c.750T= (p.Ser250=) | |
| 18 | g.53207742C>A | CA402518189 | DCC | c.1786C>A (p.Leu596Ile) c.1587C>A c.1717C>A (p.Leu573Ile) c.751C>A (p.Leu251Ile) | dbSNP gnomAD v2 gnomAD v4 |
| 18 | g.53207742C= | CA2304037515 | DCC | c.1786C= (p.Leu596=) c.1587C= c.1717C= (p.Leu573=) c.751C= (p.Leu251=) | |
| 18 | g.53207742C>G | CA402518187 | DCC | c.1786C>G (p.Leu596Val) c.1587C>G c.1717C>G (p.Leu573Val) c.751C>G (p.Leu251Val) | |
| 18 | g.53207742C>T | CA402518188 | DCC | c.1786C>T (p.Leu596Phe) c.1587C>T c.1717C>T (p.Leu573Phe) c.751C>T (p.Leu251Phe) | gnomAD v4 |
| 18 | g.53207743T>A | CA402518190 | DCC | c.1787T>A (p.Leu596His) c.1588T>A c.1718T>A (p.Leu573His) c.752T>A (p.Leu251His) | |
| 18 | g.53207743T>C | CA402518191 | DCC | c.1787T>C (p.Leu596Pro) c.1588T>C c.1718T>C (p.Leu573Pro) c.752T>C (p.Leu251Pro) | |
| 18 | g.53207743T>G | CA402518192 | DCC | c.1787T>G (p.Leu596Arg) c.1588T>G c.1718T>G (p.Leu573Arg) c.752T>G (p.Leu251Arg) | |
| 18 | g.53207744T>A | CA503971874 | DCC | c.1788T>A (p.Leu596=) c.1589T>A c.1719T>A (p.Leu573=) c.753T>A (p.Leu251=) | |
| 18 | g.53207744T>C | CA503971873 | DCC | c.1788T>C (p.Leu596=) c.1589T>C c.1719T>C (p.Leu573=) c.753T>C (p.Leu251=) | gnomAD v4 COSMIC |
| 18 | g.53207744T>G | CA503971875 | DCC | c.1788T>G (p.Leu596=) c.1589T>G c.1719T>G (p.Leu573=) c.753T>G (p.Leu251=) | |
| 18 | g.53207745C>A | CA503971876 | DCC | c.1789C>A (p.Arg597=) c.1590C>A c.1720C>A (p.Arg574=) c.754C>A (p.Arg252=) | gnomAD v4 |
| 18 | g.53207745C= | CA2304037519 | DCC | c.1789C= (p.Arg597=) c.1590C= c.1720C= (p.Arg574=) c.754C= (p.Arg252=) | |
| 18 | g.53207745C>G | CA402518193 | DCC | c.1789C>G (p.Arg597Gly) c.1590C>G c.1720C>G (p.Arg574Gly) c.754C>G (p.Arg252Gly) | dbSNP |
| 18 | g.53207745C>T | CA402518194 | DCC | c.1789C>T (p.Arg597Ter) c.1590C>T c.1720C>T (p.Arg574Ter) c.754C>T (p.Arg252Ter) | ClinVar dbSNP COSMIC COSMIC |
| 18 | g.53207746G>A | CA402518196 | DCC | c.1790G>A (p.Arg597Gln) c.1591G>A c.1721G>A (p.Arg574Gln) c.755G>A (p.Arg252Gln) | dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
| 18 | g.53207746G>C | CA16044032 | DCC | c.1790G>C (p.Arg597Pro) c.1591G>C c.1721G>C (p.Arg574Pro) c.755G>C (p.Arg252Pro) | ClinVar dbSNP |
| 18 | g.53207746G= | CA2304037522 | DCC | c.1790G= (p.Arg597=) c.1591G= c.1721G= (p.Arg574=) c.755G= (p.Arg252=) | |
| 18 | g.53207746G>T | CA402518195 | DCC | c.1790G>T (p.Arg597Leu) c.1591G>T c.1721G>T (p.Arg574Leu) c.755G>T (p.Arg252Leu) | gnomAD v4 |
| 18 | g.53207747A= | CA2304037525 | DCC | c.1791A= (p.Arg597=) c.1592A= c.1722A= (p.Arg574=) c.756A= (p.Arg252=) | |
| 18 | g.53207747A>C | CA503971877 | DCC | c.1791A>C (p.Arg597=) c.1592A>C c.1722A>C (p.Arg574=) c.756A>C (p.Arg252=) | dbSNP |
| 18 | g.53207747A>G | CA503971878 | DCC | c.1791A>G (p.Arg597=) c.1592A>G c.1722A>G (p.Arg574=) c.756A>G (p.Arg252=) | |
| 18 | g.53207747A>T | CA503971879 | DCC | c.1791A>T (p.Arg597=) c.1592A>T c.1722A>T (p.Arg574=) c.756A>T (p.Arg252=) | dbSNP gnomAD v4 |
| 18 | g.53207748T>A | CA402518197 | DCC | c.1792T>A (p.Phe598Ile) c.1593T>A c.1723T>A (p.Phe575Ile) c.757T>A (p.Phe253Ile) | |
| 18 | g.53207748T>C | CA300765519 | DCC | c.1792T>C (p.Phe598Leu) c.1593T>C c.1723T>C (p.Phe575Leu) c.757T>C (p.Phe253Leu) | dbSNP |
| 18 | g.53207748T>G | CA402518198 | DCC | c.1792T>G (p.Phe598Val) c.1593T>G c.1723T>G (p.Phe575Val) c.757T>G (p.Phe253Val) | |
| 18 | g.53207748T= | CA2304037527 | DCC | c.1792T= (p.Phe598=) c.1593T= c.1723T= (p.Phe575=) c.757T= (p.Phe253=) | |
| 18 | g.53207749T>A | CA402518199 | DCC | c.1793T>A (p.Phe598Tyr) c.1594T>A c.1724T>A (p.Phe575Tyr) c.758T>A (p.Phe253Tyr) | dbSNP gnomAD v4 |
| 18 | g.53207749T>C | CA402518200 | DCC | c.1793T>C (p.Phe598Ser) c.1594T>C c.1724T>C (p.Phe575Ser) c.758T>C (p.Phe253Ser) | dbSNP gnomAD v3 gnomAD v4 |
| 18 | g.53207749T>G | CA402518201 | DCC | c.1793T>G (p.Phe598Cys) c.1594T>G c.1724T>G (p.Phe575Cys) c.758T>G (p.Phe253Cys) | |
| 18 | g.53207749T= | CA2304037531 | DCC | c.1793T= (p.Phe598=) c.1594T= c.1724T= (p.Phe575=) c.758T= (p.Phe253=) | |
| 18 | g.53207750C>A | CA402518202 | DCC | c.1794C>A (p.Phe598Leu) c.1595C>A c.1725C>A (p.Phe575Leu) c.759C>A (p.Phe253Leu) | COSMIC |
| 18 | g.53207750C>G | CA402518203 | DCC | c.1794C>G (p.Phe598Leu) c.1595C>G c.1725C>G (p.Phe575Leu) c.759C>G (p.Phe253Leu) | |
| 18 | g.53207750C>T | CA503971880 | DCC | c.1794C>T (p.Phe598=) c.1595C>T c.1725C>T (p.Phe575=) c.759C>T (p.Phe253=) | |
| 18 | g.53207751T>A | CA402518204 | DCC | c.1795T>A (p.Leu599Ile) c.1596T>A c.1726T>A (p.Leu576Ile) c.760T>A (p.Leu254Ile) | |
| 18 | g.53207751T>C | CA503971881 | DCC | c.1795T>C (p.Leu599=) c.1596T>C c.1726T>C (p.Leu576=) c.760T>C (p.Leu254=) | |
| 18 | g.53207751T>G | CA402518205 | DCC | c.1795T>G (p.Leu599Val) c.1596T>G c.1726T>G (p.Leu576Val) c.760T>G (p.Leu254Val) | |
| 18 | g.53207752T>A | CA402518206 | DCC | c.1796T>A (p.Leu599Ter) c.1597T>A c.1727T>A (p.Leu576Ter) c.761T>A (p.Leu254Ter) | |
| 18 | g.53207752T>C | CA402518207 | DCC | c.1796T>C (p.Leu599Ser) c.1597T>C c.1727T>C (p.Leu576Ser) c.761T>C (p.Leu254Ser) | |
| 18 | g.53207752T>G | CA402518208 | DCC | c.1796T>G (p.Leu599Ter) c.1597T>G c.1727T>G (p.Leu576Ter) c.761T>G (p.Leu254Ter) | COSMIC COSMIC |
| 18 | g.53207753A= | CA2304037535 | DCC | c.1797A= (p.Leu599=) c.1598A= c.1728A= (p.Leu576=) c.762A= (p.Leu254=) | |
| 18 | g.53207753A>C | CA402518209 | DCC | c.1797A>C (p.Leu599Phe) c.1598A>C c.1728A>C (p.Leu576Phe) c.762A>C (p.Leu254Phe) | |
| 18 | g.53207753A>G | CA503971882 | DCC | c.1797A>G (p.Leu599=) c.1598A>G c.1728A>G (p.Leu576=) c.762A>G (p.Leu254=) | dbSNP |
| 18 | g.53207753A>T | CA402518210 | DCC | c.1797A>T (p.Leu599Phe) c.1598A>T c.1728A>T (p.Leu576Phe) c.762A>T (p.Leu254Phe) | gnomAD v4 |
| 18 | g.53207754G>A | CA402518213 | DCC | c.1798G>A (p.Ala600Thr) c.1599G>A c.1729G>A (p.Ala577Thr) c.763G>A (p.Ala255Thr) | |
| 18 | g.53207754G>C | CA402518211 | DCC | c.1798G>C (p.Ala600Pro) c.1599G>C c.1729G>C (p.Ala577Pro) c.763G>C (p.Ala255Pro) | |
| 18 | g.53207754G>T | CA402518212 | DCC | c.1798G>T (p.Ala600Ser) c.1599G>T c.1729G>T (p.Ala577Ser) c.763G>T (p.Ala255Ser) | |
| 18 | g.53207755C>A | CA402518214 | DCC | c.1799C>A (p.Ala600Asp) c.1600C>A c.1730C>A (p.Ala577Asp) c.764C>A (p.Ala255Asp) | |
| 18 | g.53207755C= | CA2304037538 | DCC | c.1799C= (p.Ala600=) c.1600C= c.1730C= (p.Ala577=) c.764C= (p.Ala255=) | |
| 18 | g.53207755C>G | CA402518215 | DCC | c.1799C>G (p.Ala600Gly) c.1600C>G c.1730C>G (p.Ala577Gly) c.764C>G (p.Ala255Gly) | gnomAD v4 |
| 18 | g.53207755C>T | CA8966985 | DCC | c.1799C>T (p.Ala600Val) c.1600C>T c.1730C>T (p.Ala577Val) c.764C>T (p.Ala255Val) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 18 | g.53207756T>A | CA503971883 | DCC | c.1800T>A (p.Ala600=) c.1601T>A c.1731T>A (p.Ala577=) c.765T>A (p.Ala255=) | gnomAD v4 |
| 18 | g.53207756T>C | CA503971884 | DCC | c.1800T>C (p.Ala600=) c.1601T>C c.1731T>C (p.Ala577=) c.765T>C (p.Ala255=) | |
| 18 | g.53207756T>G | CA503971885 | DCC | c.1800T>G (p.Ala600=) c.1601T>G c.1731T>G (p.Ala577=) c.765T>G (p.Ala255=) | |
| 18 | g.53207757del | CA2567003387 | DCC | c.1801del (p.Tyr601IlefsTer13) c.1602del c.1732del (p.Tyr578IlefsTer13) c.766del (p.Tyr256IlefsTer13) | |
| 18 | g.53207757T>A | CA402518216 | DCC | c.1801T>A (p.Tyr601Asn) c.1602T>A c.1732T>A (p.Tyr578Asn) c.766T>A (p.Tyr256Asn) | |
| 18 | g.53207757T>C | CA402518217 | DCC | c.1801T>C (p.Tyr601His) c.1602T>C c.1732T>C (p.Tyr578His) c.766T>C (p.Tyr256His) | |
| 18 | g.53207757T>G | CA402518218 | DCC | c.1801T>G (p.Tyr601Asp) c.1602T>G c.1732T>G (p.Tyr578Asp) c.766T>G (p.Tyr256Asp) | |
| 18 | g.53207758A>C | CA402518219 | DCC | c.1802A>C (p.Tyr601Ser) c.1603A>C c.1733A>C (p.Tyr578Ser) c.767A>C (p.Tyr256Ser) | |
| 18 | g.53207758A>G | CA402518220 | DCC | c.1802A>G (p.Tyr601Cys) c.1603A>G c.1733A>G (p.Tyr578Cys) c.767A>G (p.Tyr256Cys) | |
| 18 | g.53207758A>T | CA402518221 | DCC | c.1802A>T (p.Tyr601Phe) c.1603A>T c.1733A>T (p.Tyr578Phe) c.767A>T (p.Tyr256Phe) | |
| 18 | g.53207759T>A | CA402518222 | DCC | c.1803T>A (p.Tyr601Ter) c.1604T>A c.1734T>A (p.Tyr578Ter) c.768T>A (p.Tyr256Ter) | |
| 18 | g.53207759T>C | CA503971886 | DCC | c.1803T>C (p.Tyr601=) c.1604T>C c.1734T>C (p.Tyr578=) c.768T>C (p.Tyr256=) | gnomAD v4 |
| 18 | g.53207759T>G | CA402518223 | DCC | c.1803T>G (p.Tyr601Ter) c.1604T>G c.1734T>G (p.Tyr578Ter) c.768T>G (p.Tyr256Ter) | |
| 18 | g.53207760A>C | CA402518226 | DCC | c.1804A>C (p.Asn602His) c.1605A>C c.1735A>C (p.Asn579His) c.769A>C (p.Asn257His) | |
| 18 | g.53207760A>G | CA402518225 | DCC | c.1804A>G (p.Asn602Asp) c.1605A>G c.1735A>G (p.Asn579Asp) c.769A>G (p.Asn257Asp) | |
| 18 | g.53207760A>T | CA402518224 | DCC | c.1804A>T (p.Asn602Tyr) c.1605A>T c.1735A>T (p.Asn579Tyr) c.769A>T (p.Asn257Tyr) | |
| 18 | g.53207761A= | CA2304037541 | DCC | c.1805A= (p.Asn602=) c.1606A= c.1736A= (p.Asn579=) c.770A= (p.Asn257=) | |
| 18 | g.53207761A>C | CA402518227 | DCC | c.1805A>C (p.Asn602Thr) c.1606A>C c.1736A>C (p.Asn579Thr) c.770A>C (p.Asn257Thr) | dbSNP gnomAD v2 gnomAD v4 |
| 18 | g.53207761A>G | CA402518228 | DCC | c.1805A>G (p.Asn602Ser) c.1606A>G c.1736A>G (p.Asn579Ser) c.770A>G (p.Asn257Ser) | COSMIC |
| 18 | g.53207761A>T | CA402518229 | DCC | c.1805A>T (p.Asn602Ile) c.1606A>T c.1736A>T (p.Asn579Ile) c.770A>T (p.Asn257Ile) | |
| 18 | g.53207762T>A | CA402518230 | DCC | c.1806T>A (p.Asn602Lys) c.1607T>A c.1737T>A (p.Asn579Lys) c.771T>A (p.Asn257Lys) | |
| 18 | g.53207762T>C | CA503971887 | DCC | c.1806T>C (p.Asn602=) c.1607T>C c.1737T>C (p.Asn579=) c.771T>C (p.Asn257=) | |
| 18 | g.53207762T>G | CA402518231 | DCC | c.1806T>G (p.Asn602Lys) c.1607T>G c.1737T>G (p.Asn579Lys) c.771T>G (p.Asn257Lys) | |
| 18 | g.53207763C>A | CA402518233 | DCC | c.1807C>A (p.Arg603Ser) c.1608C>A c.1738C>A (p.Arg580Ser) c.772C>A (p.Arg258Ser) | dbSNP |
| 18 | g.53207763C= | CA2304037543 | DCC | c.1807C= (p.Arg603=) c.1608C= c.1738C= (p.Arg580=) c.772C= (p.Arg258=) | |
| 18 | g.53207763C>G | CA402518232 | DCC | c.1807C>G (p.Arg603Gly) c.1608C>G c.1738C>G (p.Arg580Gly) c.772C>G (p.Arg258Gly) | gnomAD v4 |
| 18 | g.53207763C>T | CA8966986 | DCC | c.1807C>T (p.Arg603Cys) c.1608C>T c.1738C>T (p.Arg580Cys) c.772C>T (p.Arg258Cys) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |