Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.98393909_98399093del | CA2499216316 | CNGA3 | c.785-1935_*1838del c.839-1935_*1838del | ClinVar |
2 | g.98396750T>A | CA347833854 | CNGA3 | c.1580T>A (p.Leu527Gln) c.1592T>A (p.Leu531Gln) c.1526T>A (p.Leu509Gln) c.1691T>A (p.Leu564Gln) c.1745T>A (p.Leu582Gln) | |
2 | g.98396750T>C | CA347833853 | CNGA3 | c.1580T>C (p.Leu527Pro) c.1592T>C (p.Leu531Pro) c.1526T>C (p.Leu509Pro) c.1691T>C (p.Leu564Pro) c.1745T>C (p.Leu582Pro) | ClinVar dbSNP COSMIC |
2 | g.98396750T>G | CA1794043 | CNGA3 | c.1580T>G (p.Leu527Arg) c.1592T>G (p.Leu531Arg) c.1526T>G (p.Leu509Arg) c.1691T>G (p.Leu564Arg) c.1745T>G (p.Leu582Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.98396750T= | CA1273420049 | CNGA3 | c.1580T= (p.Leu527=) c.1592T= (p.Leu531=) c.1526T= (p.Leu509=) c.1691T= (p.Leu564=) c.1745T= (p.Leu582=) | |
2 | g.98396751G>A | CA427820183 | CNGA3 | c.1581G>A (p.Leu527=) c.1593G>A (p.Leu531=) c.1527G>A (p.Leu509=) c.1692G>A (p.Leu564=) c.1746G>A (p.Leu582=) | |
2 | g.98396751G>C | CA427820184 | CNGA3 | c.1581G>C (p.Leu527=) c.1593G>C (p.Leu531=) c.1527G>C (p.Leu509=) c.1692G>C (p.Leu564=) c.1746G>C (p.Leu582=) | |
2 | g.98396751G>T | CA427820185 | CNGA3 | c.1581G>T (p.Leu527=) c.1593G>T (p.Leu531=) c.1527G>T (p.Leu509=) c.1692G>T (p.Leu564=) c.1746G>T (p.Leu582=) | |
2 | g.98396752G>A | CA347833855 | CNGA3 | c.1582G>A (p.Ala528Thr) c.1594G>A (p.Ala532Thr) c.1528G>A (p.Ala510Thr) c.1693G>A (p.Ala565Thr) c.1747G>A (p.Ala583Thr) | |
2 | g.98396752G>C | CA347833856 | CNGA3 | c.1582G>C (p.Ala528Pro) c.1594G>C (p.Ala532Pro) c.1528G>C (p.Ala510Pro) c.1693G>C (p.Ala565Pro) c.1747G>C (p.Ala583Pro) | |
2 | g.98396752G>T | CA347833857 | CNGA3 | c.1582G>T (p.Ala528Ser) c.1594G>T (p.Ala532Ser) c.1528G>T (p.Ala510Ser) c.1693G>T (p.Ala565Ser) c.1747G>T (p.Ala583Ser) | |
2 | g.98396753C>A | CA347833858 | CNGA3 | c.1583C>A (p.Ala528Asp) c.1595C>A (p.Ala532Asp) c.1529C>A (p.Ala510Asp) c.1694C>A (p.Ala565Asp) c.1748C>A (p.Ala583Asp) | |
2 | g.98396753C>G | CA347833859 | CNGA3 | c.1583C>G (p.Ala528Gly) c.1595C>G (p.Ala532Gly) c.1529C>G (p.Ala510Gly) c.1694C>G (p.Ala565Gly) c.1748C>G (p.Ala583Gly) | |
2 | g.98396753C>T | CA347833860 | CNGA3 | c.1583C>T (p.Ala528Val) c.1595C>T (p.Ala532Val) c.1529C>T (p.Ala510Val) c.1694C>T (p.Ala565Val) c.1748C>T (p.Ala583Val) | COSMIC |
2 | g.98396754C>A | CA427820191 | CNGA3 | c.1584C>A (p.Ala528=) c.1596C>A (p.Ala532=) c.1530C>A (p.Ala510=) c.1695C>A (p.Ala565=) c.1749C>A (p.Ala583=) | ClinVar dbSNP gnomAD v4 |
2 | g.98396754C= | CA1273420050 | CNGA3 | c.1584C= (p.Ala528=) c.1596C= (p.Ala532=) c.1530C= (p.Ala510=) c.1695C= (p.Ala565=) c.1749C= (p.Ala583=) | |
2 | g.98396754C>G | CA427820193 | CNGA3 | c.1584C>G (p.Ala528=) c.1596C>G (p.Ala532=) c.1530C>G (p.Ala510=) c.1695C>G (p.Ala565=) c.1749C>G (p.Ala583=) | |
2 | g.98396754C>T | CA1794044 | CNGA3 | c.1584C>T (p.Ala528=) c.1596C>T (p.Ala532=) c.1530C>T (p.Ala510=) c.1695C>T (p.Ala565=) c.1749C>T (p.Ala583=) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
2 | g.98396755G>A | CA254826 | CNGA3 | c.1585G>A (p.Val529Met) c.1597G>A (p.Val533Met) c.1531G>A (p.Val511Met) c.1696G>A (p.Val566Met) c.1750G>A (p.Val584Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
2 | g.98396755G>C | CA347833861 | CNGA3 | c.1585G>C (p.Val529Leu) c.1597G>C (p.Val533Leu) c.1531G>C (p.Val511Leu) c.1696G>C (p.Val566Leu) c.1750G>C (p.Val584Leu) | gnomAD v4 |
2 | g.98396755G= | CA1273420051 | CNGA3 | c.1585G= (p.Val529=) c.1597G= (p.Val533=) c.1531G= (p.Val511=) c.1696G= (p.Val566=) c.1750G= (p.Val584=) | |
2 | g.98396755G>T | CA347833862 | CNGA3 | c.1585G>T (p.Val529Leu) c.1597G>T (p.Val533Leu) c.1531G>T (p.Val511Leu) c.1696G>T (p.Val566Leu) c.1750G>T (p.Val584Leu) | COSMIC |
2 | g.98396756T>A | CA347833863 | CNGA3 | c.1586T>A (p.Val529Glu) c.1598T>A (p.Val533Glu) c.1532T>A (p.Val511Glu) c.1697T>A (p.Val566Glu) c.1751T>A (p.Val584Glu) | |
2 | g.98396756T>C | CA52635874 | CNGA3 | c.1586T>C (p.Val529Ala) c.1598T>C (p.Val533Ala) c.1532T>C (p.Val511Ala) c.1697T>C (p.Val566Ala) c.1751T>C (p.Val584Ala) | dbSNP |
2 | g.98396756T>G | CA347833864 | CNGA3 | c.1586T>G (p.Val529Gly) c.1598T>G (p.Val533Gly) c.1532T>G (p.Val511Gly) c.1697T>G (p.Val566Gly) c.1751T>G (p.Val584Gly) | |
2 | g.98396756T= | CA1273420052 | CNGA3 | c.1586T= (p.Val529=) c.1598T= (p.Val533=) c.1532T= (p.Val511=) c.1697T= (p.Val566=) c.1751T= (p.Val584=) | |
2 | g.98396757G>A | CA427820195 | CNGA3 | c.1587G>A (p.Val529=) c.1599G>A (p.Val533=) c.1533G>A (p.Val511=) c.1698G>A (p.Val566=) c.1752G>A (p.Val584=) | gnomAD v4 |
2 | g.98396757G>C | CA427820197 | CNGA3 | c.1587G>C (p.Val529=) c.1599G>C (p.Val533=) c.1533G>C (p.Val511=) c.1698G>C (p.Val566=) c.1752G>C (p.Val584=) | |
2 | g.98396757G>T | CA427820198 | CNGA3 | c.1587G>T (p.Val529=) c.1599G>T (p.Val533=) c.1533G>T (p.Val511=) c.1698G>T (p.Val566=) c.1752G>T (p.Val584=) | |
2 | g.98396758G>A | CA347833866 | CNGA3 | c.1588G>A (p.Val530Met) c.1600G>A (p.Val534Met) c.1534G>A (p.Val512Met) c.1699G>A (p.Val567Met) c.1753G>A (p.Val585Met) | |
2 | g.98396758G>C | CA347833867 | CNGA3 | c.1588G>C (p.Val530Leu) c.1600G>C (p.Val534Leu) c.1534G>C (p.Val512Leu) c.1699G>C (p.Val567Leu) c.1753G>C (p.Val585Leu) | |
2 | g.98396758G= | CA1273420053 | CNGA3 | c.1588G= (p.Val530=) c.1600G= (p.Val534=) c.1534G= (p.Val512=) c.1699G= (p.Val567=) c.1753G= (p.Val585=) | |
2 | g.98396758G>T | CA347833865 | CNGA3 | c.1588G>T (p.Val530Leu) c.1600G>T (p.Val534Leu) c.1534G>T (p.Val512Leu) c.1699G>T (p.Val567Leu) c.1753G>T (p.Val585Leu) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.98396759T>A | CA347833869 | CNGA3 | c.1589T>A (p.Val530Glu) c.1601T>A (p.Val534Glu) c.1535T>A (p.Val512Glu) c.1700T>A (p.Val567Glu) c.1754T>A (p.Val585Glu) | |
2 | g.98396759T>C | CA347833868 | CNGA3 | c.1589T>C (p.Val530Ala) c.1601T>C (p.Val534Ala) c.1535T>C (p.Val512Ala) c.1700T>C (p.Val567Ala) c.1754T>C (p.Val585Ala) | |
2 | g.98396759T>G | CA347833870 | CNGA3 | c.1589T>G (p.Val530Gly) c.1601T>G (p.Val534Gly) c.1535T>G (p.Val512Gly) c.1700T>G (p.Val567Gly) c.1754T>G (p.Val585Gly) | |
2 | g.98396760G>A | CA427820204 | CNGA3 | c.1590G>A (p.Val530=) c.1602G>A (p.Val534=) c.1536G>A (p.Val512=) c.1701G>A (p.Val567=) c.1755G>A (p.Val585=) | dbSNP gnomAD v4 |
2 | g.98396760G>C | CA427820207 | CNGA3 | c.1590G>C (p.Val530=) c.1602G>C (p.Val534=) c.1536G>C (p.Val512=) c.1701G>C (p.Val567=) c.1755G>C (p.Val585=) | |
2 | g.98396760G= | CA1273420054 | CNGA3 | c.1590G= (p.Val530=) c.1602G= (p.Val534=) c.1536G= (p.Val512=) c.1701G= (p.Val567=) c.1755G= (p.Val585=) | |
2 | g.98396760G>T | CA427820208 | CNGA3 | c.1590G>T (p.Val530=) c.1602G>T (p.Val534=) c.1536G>T (p.Val512=) c.1701G>T (p.Val567=) c.1755G>T (p.Val585=) | |
2 | g.98396761G>A | CA347833871 | CNGA3 | c.1591G>A (p.Ala531Thr) c.1603G>A (p.Ala535Thr) c.1537G>A (p.Ala513Thr) c.1702G>A (p.Ala568Thr) c.1756G>A (p.Ala586Thr) | |
2 | g.98396761G>C | CA347833872 | CNGA3 | c.1591G>C (p.Ala531Pro) c.1603G>C (p.Ala535Pro) c.1537G>C (p.Ala513Pro) c.1702G>C (p.Ala568Pro) c.1756G>C (p.Ala586Pro) | |
2 | g.98396761G>T | CA347833873 | CNGA3 | c.1591G>T (p.Ala531Ser) c.1603G>T (p.Ala535Ser) c.1537G>T (p.Ala513Ser) c.1702G>T (p.Ala568Ser) c.1756G>T (p.Ala586Ser) | |
2 | g.98396762C>A | CA347833874 | CNGA3 | c.1592C>A (p.Ala531Asp) c.1604C>A (p.Ala535Asp) c.1538C>A (p.Ala513Asp) c.1703C>A (p.Ala568Asp) c.1757C>A (p.Ala586Asp) | |
2 | g.98396762C= | CA1273420055 | CNGA3 | c.1592C= (p.Ala531=) c.1604C= (p.Ala535=) c.1538C= (p.Ala513=) c.1703C= (p.Ala568=) c.1757C= (p.Ala586=) | |
2 | g.98396762C>G | CA347833875 | CNGA3 | c.1592C>G (p.Ala531Gly) c.1604C>G (p.Ala535Gly) c.1538C>G (p.Ala513Gly) c.1703C>G (p.Ala568Gly) c.1757C>G (p.Ala586Gly) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.98396762C>T | CA347833876 | CNGA3 | c.1592C>T (p.Ala531Val) c.1604C>T (p.Ala535Val) c.1538C>T (p.Ala513Val) c.1703C>T (p.Ala568Val) c.1757C>T (p.Ala586Val) | |
2 | g.98396763T>A | CA427820213 | CNGA3 | c.1593T>A (p.Ala531=) c.1605T>A (p.Ala535=) c.1539T>A (p.Ala513=) c.1704T>A (p.Ala568=) c.1758T>A (p.Ala586=) | COSMIC |
2 | g.98396763T>C | CA52635877 | CNGA3 | c.1593T>C (p.Ala531=) c.1605T>C (p.Ala535=) c.1539T>C (p.Ala513=) c.1704T>C (p.Ala568=) c.1758T>C (p.Ala586=) | dbSNP gnomAD v4 |
2 | g.98396763T>G | CA427820215 | CNGA3 | c.1593T>G (p.Ala531=) c.1605T>G (p.Ala535=) c.1539T>G (p.Ala513=) c.1704T>G (p.Ala568=) c.1758T>G (p.Ala586=) |