| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.78714783C>A | CA390755793 | NRXN3 | c.1688C>A (p.Thr563Lys) c.1700C>A (p.Thr567Lys) c.931C>A c.971C>A (p.Thr324Lys) c.569C>A (p.Thr190Lys) c.1682C>A (p.Thr561Lys) n.1032C>A n.931C>A n.2687C>A c.1724C>A (p.Thr575Lys) c.1712C>A (p.Thr571Lys) c.632C>A (p.Thr211Lys) n.2729C>A n.2705C>A n.2693C>A c.1664C>A (p.Thr555Lys) | gnomAD v4 |
| 14 | g.78714783C= | CA2148986578 | NRXN3 | c.1688C= (p.Thr563=) c.1700C= (p.Thr567=) c.931C= c.971C= (p.Thr324=) c.569C= (p.Thr190=) c.1682C= (p.Thr561=) n.1032C= n.931C= n.2687C= c.1724C= (p.Thr575=) c.1712C= (p.Thr571=) c.632C= (p.Thr211=) n.2729C= n.2705C= n.2693C= c.1664C= (p.Thr555=) | |
| 14 | g.78714783C>G | CA390755794 | NRXN3 | c.1688C>G (p.Thr563Arg) c.1700C>G (p.Thr567Arg) c.931C>G c.971C>G (p.Thr324Arg) c.569C>G (p.Thr190Arg) c.1682C>G (p.Thr561Arg) n.1032C>G n.931C>G n.2687C>G c.1724C>G (p.Thr575Arg) c.1712C>G (p.Thr571Arg) c.632C>G (p.Thr211Arg) n.2729C>G n.2705C>G n.2693C>G c.1664C>G (p.Thr555Arg) | |
| 14 | g.78714783C>T | CA264121817 | NRXN3 | c.1688C>T (p.Thr563Met) c.1700C>T (p.Thr567Met) c.931C>T c.971C>T (p.Thr324Met) c.569C>T (p.Thr190Met) c.1682C>T (p.Thr561Met) n.1032C>T n.931C>T n.2687C>T c.1724C>T (p.Thr575Met) c.1712C>T (p.Thr571Met) c.632C>T (p.Thr211Met) n.2729C>T n.2705C>T n.2693C>T c.1664C>T (p.Thr555Met) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.78714784G>A | CA7291699 | NRXN3 | c.1689G>A (p.Thr563=) c.1701G>A (p.Thr567=) c.932G>A c.972G>A (p.Thr324=) c.570G>A (p.Thr190=) c.1683G>A (p.Thr561=) n.1033G>A n.932G>A n.2688G>A c.1725G>A (p.Thr575=) c.1713G>A (p.Thr571=) c.633G>A (p.Thr211=) n.2730G>A n.2706G>A n.2694G>A c.1665G>A (p.Thr555=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.78714784G>C | CA487515890 | NRXN3 | c.1689G>C (p.Thr563=) c.1701G>C (p.Thr567=) c.932G>C c.972G>C (p.Thr324=) c.570G>C (p.Thr190=) c.1683G>C (p.Thr561=) n.1033G>C n.932G>C n.2688G>C c.1725G>C (p.Thr575=) c.1713G>C (p.Thr571=) c.633G>C (p.Thr211=) n.2730G>C n.2706G>C n.2694G>C c.1665G>C (p.Thr555=) | |
| 14 | g.78714784G= | CA2148986579 | NRXN3 | c.1689G= (p.Thr563=) c.1701G= (p.Thr567=) c.932G= c.972G= (p.Thr324=) c.570G= (p.Thr190=) c.1683G= (p.Thr561=) n.1033G= n.932G= n.2688G= c.1725G= (p.Thr575=) c.1713G= (p.Thr571=) c.633G= (p.Thr211=) n.2730G= n.2706G= n.2694G= c.1665G= (p.Thr555=) | |
| 14 | g.78714784G>T | CA487515891 | NRXN3 | c.1689G>T (p.Thr563=) c.1701G>T (p.Thr567=) c.932G>T c.972G>T (p.Thr324=) c.570G>T (p.Thr190=) c.1683G>T (p.Thr561=) n.1033G>T n.932G>T n.2688G>T c.1725G>T (p.Thr575=) c.1713G>T (p.Thr571=) c.633G>T (p.Thr211=) n.2730G>T n.2706G>T n.2694G>T c.1665G>T (p.Thr555=) | |
| 14 | g.78714785C>A | CA390755795 | NRXN3 | c.1690C>A (p.Pro564Thr) c.1702C>A (p.Pro568Thr) c.933C>A c.973C>A (p.Pro325Thr) c.571C>A (p.Pro191Thr) c.1684C>A (p.Pro562Thr) n.1034C>A n.933C>A n.2689C>A c.1726C>A (p.Pro576Thr) c.1714C>A (p.Pro572Thr) c.634C>A (p.Pro212Thr) n.2731C>A n.2707C>A n.2695C>A c.1666C>A (p.Pro556Thr) | |
| 14 | g.78714785C>G | CA390755797 | NRXN3 | c.1690C>G (p.Pro564Ala) c.1702C>G (p.Pro568Ala) c.933C>G c.973C>G (p.Pro325Ala) c.571C>G (p.Pro191Ala) c.1684C>G (p.Pro562Ala) n.1034C>G n.933C>G n.2689C>G c.1726C>G (p.Pro576Ala) c.1714C>G (p.Pro572Ala) c.634C>G (p.Pro212Ala) n.2731C>G n.2707C>G n.2695C>G c.1666C>G (p.Pro556Ala) | |
| 14 | g.78714785C>T | CA390755796 | NRXN3 | c.1690C>T (p.Pro564Ser) c.1702C>T (p.Pro568Ser) c.933C>T c.973C>T (p.Pro325Ser) c.571C>T (p.Pro191Ser) c.1684C>T (p.Pro562Ser) n.1034C>T n.933C>T n.2689C>T c.1726C>T (p.Pro576Ser) c.1714C>T (p.Pro572Ser) c.634C>T (p.Pro212Ser) n.2731C>T n.2707C>T n.2695C>T c.1666C>T (p.Pro556Ser) | gnomAD v4 |
| 14 | g.78714786C>A | CA390755798 | NRXN3 | c.1691C>A (p.Pro564Gln) c.1703C>A (p.Pro568Gln) c.934C>A c.974C>A (p.Pro325Gln) c.572C>A (p.Pro191Gln) c.1685C>A (p.Pro562Gln) n.1035C>A n.934C>A n.2690C>A c.1727C>A (p.Pro576Gln) c.1715C>A (p.Pro572Gln) c.635C>A (p.Pro212Gln) n.2732C>A n.2708C>A n.2696C>A c.1667C>A (p.Pro556Gln) | dbSNP |
| 14 | g.78714786C= | CA2148986580 | NRXN3 | c.1691C= (p.Pro564=) c.1703C= (p.Pro568=) c.934C= c.974C= (p.Pro325=) c.572C= (p.Pro191=) c.1685C= (p.Pro562=) n.1035C= n.934C= n.2690C= c.1727C= (p.Pro576=) c.1715C= (p.Pro572=) c.635C= (p.Pro212=) n.2732C= n.2708C= n.2696C= c.1667C= (p.Pro556=) | |
| 14 | g.78714786C>G | CA390755799 | NRXN3 | c.1691C>G (p.Pro564Arg) c.1703C>G (p.Pro568Arg) c.934C>G c.974C>G (p.Pro325Arg) c.572C>G (p.Pro191Arg) c.1685C>G (p.Pro562Arg) n.1035C>G n.934C>G n.2690C>G c.1727C>G (p.Pro576Arg) c.1715C>G (p.Pro572Arg) c.635C>G (p.Pro212Arg) n.2732C>G n.2708C>G n.2696C>G c.1667C>G (p.Pro556Arg) | |
| 14 | g.78714786C>T | CA390755800 | NRXN3 | c.1691C>T (p.Pro564Leu) c.1703C>T (p.Pro568Leu) c.934C>T c.974C>T (p.Pro325Leu) c.572C>T (p.Pro191Leu) c.1685C>T (p.Pro562Leu) n.1035C>T n.934C>T n.2690C>T c.1727C>T (p.Pro576Leu) c.1715C>T (p.Pro572Leu) c.635C>T (p.Pro212Leu) n.2732C>T n.2708C>T n.2696C>T c.1667C>T (p.Pro556Leu) | |
| 14 | g.78714787A= | CA2148986581 | NRXN3 | c.1692A= (p.Pro564=) c.1704A= (p.Pro568=) c.935A= c.975A= (p.Pro325=) c.573A= (p.Pro191=) c.1686A= (p.Pro562=) n.1036A= n.935A= n.2691A= c.1728A= (p.Pro576=) c.1716A= (p.Pro572=) c.636A= (p.Pro212=) n.2733A= n.2709A= n.2697A= c.1668A= (p.Pro556=) | |
| 14 | g.78714787A>C | CA487515893 | NRXN3 | c.1692A>C (p.Pro564=) c.1704A>C (p.Pro568=) c.935A>C c.975A>C (p.Pro325=) c.573A>C (p.Pro191=) c.1686A>C (p.Pro562=) n.1036A>C n.935A>C n.2691A>C c.1728A>C (p.Pro576=) c.1716A>C (p.Pro572=) c.636A>C (p.Pro212=) n.2733A>C n.2709A>C n.2697A>C c.1668A>C (p.Pro556=) | |
| 14 | g.78714787A>G | CA487515892 | NRXN3 | c.1692A>G (p.Pro564=) c.1704A>G (p.Pro568=) c.935A>G c.975A>G (p.Pro325=) c.573A>G (p.Pro191=) c.1686A>G (p.Pro562=) n.1036A>G n.935A>G n.2691A>G c.1728A>G (p.Pro576=) c.1716A>G (p.Pro572=) c.636A>G (p.Pro212=) n.2733A>G n.2709A>G n.2697A>G c.1668A>G (p.Pro556=) | gnomAD v4 |
| 14 | g.78714787A>T | CA264121818 | NRXN3 | c.1692A>T (p.Pro564=) c.1704A>T (p.Pro568=) c.935A>T c.975A>T (p.Pro325=) c.573A>T (p.Pro191=) c.1686A>T (p.Pro562=) n.1036A>T n.935A>T n.2691A>T c.1728A>T (p.Pro576=) c.1716A>T (p.Pro572=) c.636A>T (p.Pro212=) n.2733A>T n.2709A>T n.2697A>T c.1668A>T (p.Pro556=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.78714788T>A | CA390755801 | NRXN3 | c.1693T>A (p.Phe565Ile) c.1705T>A (p.Phe569Ile) c.936T>A c.976T>A (p.Phe326Ile) c.574T>A (p.Phe192Ile) c.1687T>A (p.Phe563Ile) n.1037T>A n.936T>A n.2692T>A c.1729T>A (p.Phe577Ile) c.1717T>A (p.Phe573Ile) c.637T>A (p.Phe213Ile) n.2734T>A n.2710T>A n.2698T>A c.1669T>A (p.Phe557Ile) | |
| 14 | g.78714788T>C | CA390755802 | NRXN3 | c.1693T>C (p.Phe565Leu) c.1705T>C (p.Phe569Leu) c.936T>C c.976T>C (p.Phe326Leu) c.574T>C (p.Phe192Leu) c.1687T>C (p.Phe563Leu) n.1037T>C n.936T>C n.2692T>C c.1729T>C (p.Phe577Leu) c.1717T>C (p.Phe573Leu) c.637T>C (p.Phe213Leu) n.2734T>C n.2710T>C n.2698T>C c.1669T>C (p.Phe557Leu) | |
| 14 | g.78714788T>G | CA390755803 | NRXN3 | c.1693T>G (p.Phe565Val) c.1705T>G (p.Phe569Val) c.936T>G c.976T>G (p.Phe326Val) c.574T>G (p.Phe192Val) c.1687T>G (p.Phe563Val) n.1037T>G n.936T>G n.2692T>G c.1729T>G (p.Phe577Val) c.1717T>G (p.Phe573Val) c.637T>G (p.Phe213Val) n.2734T>G n.2710T>G n.2698T>G c.1669T>G (p.Phe557Val) | |
| 14 | g.78714789T>A | CA390755804 | NRXN3 | c.1694T>A (p.Phe565Tyr) c.1706T>A (p.Phe569Tyr) c.937T>A c.977T>A (p.Phe326Tyr) c.575T>A (p.Phe192Tyr) c.1688T>A (p.Phe563Tyr) n.1038T>A n.937T>A n.2693T>A c.1730T>A (p.Phe577Tyr) c.1718T>A (p.Phe573Tyr) c.638T>A (p.Phe213Tyr) n.2735T>A n.2711T>A n.2699T>A c.1670T>A (p.Phe557Tyr) | |
| 14 | g.78714789T>C | CA390755805 | NRXN3 | c.1694T>C (p.Phe565Ser) c.1706T>C (p.Phe569Ser) c.937T>C c.977T>C (p.Phe326Ser) c.575T>C (p.Phe192Ser) c.1688T>C (p.Phe563Ser) n.1038T>C n.937T>C n.2693T>C c.1730T>C (p.Phe577Ser) c.1718T>C (p.Phe573Ser) c.638T>C (p.Phe213Ser) n.2735T>C n.2711T>C n.2699T>C c.1670T>C (p.Phe557Ser) | |
| 14 | g.78714789T>G | CA390755806 | NRXN3 | c.1694T>G (p.Phe565Cys) c.1706T>G (p.Phe569Cys) c.937T>G c.977T>G (p.Phe326Cys) c.575T>G (p.Phe192Cys) c.1688T>G (p.Phe563Cys) n.1038T>G n.937T>G n.2693T>G c.1730T>G (p.Phe577Cys) c.1718T>G (p.Phe573Cys) c.638T>G (p.Phe213Cys) n.2735T>G n.2711T>G n.2699T>G c.1670T>G (p.Phe557Cys) | |
| 14 | g.78714790C>A | CA390755807 | NRXN3 | c.1695C>A (p.Phe565Leu) c.1707C>A (p.Phe569Leu) c.938C>A c.978C>A (p.Phe326Leu) c.576C>A (p.Phe192Leu) c.1689C>A (p.Phe563Leu) n.1039C>A n.938C>A n.2694C>A c.1731C>A (p.Phe577Leu) c.1719C>A (p.Phe573Leu) c.639C>A (p.Phe213Leu) n.2736C>A n.2712C>A n.2700C>A c.1671C>A (p.Phe557Leu) | |
| 14 | g.78714790C>G | CA390755808 | NRXN3 | c.1695C>G (p.Phe565Leu) c.1707C>G (p.Phe569Leu) c.938C>G c.978C>G (p.Phe326Leu) c.576C>G (p.Phe192Leu) c.1689C>G (p.Phe563Leu) n.1039C>G n.938C>G n.2694C>G c.1731C>G (p.Phe577Leu) c.1719C>G (p.Phe573Leu) c.639C>G (p.Phe213Leu) n.2736C>G n.2712C>G n.2700C>G c.1671C>G (p.Phe557Leu) | |
| 14 | g.78714790C>T | CA487515894 | NRXN3 | c.1695C>T (p.Phe565=) c.1707C>T (p.Phe569=) c.938C>T c.978C>T (p.Phe326=) c.576C>T (p.Phe192=) c.1689C>T (p.Phe563=) n.1039C>T n.938C>T n.2694C>T c.1731C>T (p.Phe577=) c.1719C>T (p.Phe573=) c.639C>T (p.Phe213=) n.2736C>T n.2712C>T n.2700C>T c.1671C>T (p.Phe557=) | COSMIC |
| 14 | g.78714791A= | CA2148986582 | NRXN3 | c.1696A= (p.Thr566=) c.1708A= (p.Thr570=) c.939A= c.979A= (p.Thr327=) c.577A= (p.Thr193=) c.1690A= (p.Thr564=) n.1040A= n.939A= n.2695A= c.1732A= (p.Thr578=) c.1720A= (p.Thr574=) c.640A= (p.Thr214=) n.2737A= n.2713A= n.2701A= c.1672A= (p.Thr558=) | |
| 14 | g.78714791A>C | CA390755811 | NRXN3 | c.1696A>C (p.Thr566Pro) c.1708A>C (p.Thr570Pro) c.939A>C c.979A>C (p.Thr327Pro) c.577A>C (p.Thr193Pro) c.1690A>C (p.Thr564Pro) n.1040A>C n.939A>C n.2695A>C c.1732A>C (p.Thr578Pro) c.1720A>C (p.Thr574Pro) c.640A>C (p.Thr214Pro) n.2737A>C n.2713A>C n.2701A>C c.1672A>C (p.Thr558Pro) | dbSNP |
| 14 | g.78714791A>G | CA390755809 | NRXN3 | c.1696A>G (p.Thr566Ala) c.1708A>G (p.Thr570Ala) c.939A>G c.979A>G (p.Thr327Ala) c.577A>G (p.Thr193Ala) c.1690A>G (p.Thr564Ala) n.1040A>G n.939A>G n.2695A>G c.1732A>G (p.Thr578Ala) c.1720A>G (p.Thr574Ala) c.640A>G (p.Thr214Ala) n.2737A>G n.2713A>G n.2701A>G c.1672A>G (p.Thr558Ala) | gnomAD v4 |
| 14 | g.78714791A>T | CA390755810 | NRXN3 | c.1696A>T (p.Thr566Ser) c.1708A>T (p.Thr570Ser) c.939A>T c.979A>T (p.Thr327Ser) c.577A>T (p.Thr193Ser) c.1690A>T (p.Thr564Ser) n.1040A>T n.939A>T n.2695A>T c.1732A>T (p.Thr578Ser) c.1720A>T (p.Thr574Ser) c.640A>T (p.Thr214Ser) n.2737A>T n.2713A>T n.2701A>T c.1672A>T (p.Thr558Ser) | |
| 14 | g.78714792C>A | CA390755812 | NRXN3 | c.1697C>A (p.Thr566Asn) c.1709C>A (p.Thr570Asn) c.940C>A c.980C>A (p.Thr327Asn) c.578C>A (p.Thr193Asn) c.1691C>A (p.Thr564Asn) n.1041C>A n.940C>A n.2696C>A c.1733C>A (p.Thr578Asn) c.1721C>A (p.Thr574Asn) c.641C>A (p.Thr214Asn) n.2738C>A n.2714C>A n.2702C>A c.1673C>A (p.Thr558Asn) | |
| 14 | g.78714792C>G | CA390755813 | NRXN3 | c.1697C>G (p.Thr566Ser) c.1709C>G (p.Thr570Ser) c.940C>G c.980C>G (p.Thr327Ser) c.578C>G (p.Thr193Ser) c.1691C>G (p.Thr564Ser) n.1041C>G n.940C>G n.2696C>G c.1733C>G (p.Thr578Ser) c.1721C>G (p.Thr574Ser) c.641C>G (p.Thr214Ser) n.2738C>G n.2714C>G n.2702C>G c.1673C>G (p.Thr558Ser) | |
| 14 | g.78714792C>T | CA390755814 | NRXN3 | c.1697C>T (p.Thr566Ile) c.1709C>T (p.Thr570Ile) c.940C>T c.980C>T (p.Thr327Ile) c.578C>T (p.Thr193Ile) c.1691C>T (p.Thr564Ile) n.1041C>T n.940C>T n.2696C>T c.1733C>T (p.Thr578Ile) c.1721C>T (p.Thr574Ile) c.641C>T (p.Thr214Ile) n.2738C>T n.2714C>T n.2702C>T c.1673C>T (p.Thr558Ile) | COSMIC |
| 14 | g.78714793C>A | CA487515896 | NRXN3 | c.1698C>A (p.Thr566=) c.1710C>A (p.Thr570=) c.941C>A c.981C>A (p.Thr327=) c.579C>A (p.Thr193=) c.1692C>A (p.Thr564=) n.1042C>A n.941C>A n.2697C>A c.1734C>A (p.Thr578=) c.1722C>A (p.Thr574=) c.642C>A (p.Thr214=) n.2739C>A n.2715C>A n.2703C>A c.1674C>A (p.Thr558=) | |
| 14 | g.78714793C= | CA2148986583 | NRXN3 | c.1698C= (p.Thr566=) c.1710C= (p.Thr570=) c.941C= c.981C= (p.Thr327=) c.579C= (p.Thr193=) c.1692C= (p.Thr564=) n.1042C= n.941C= n.2697C= c.1734C= (p.Thr578=) c.1722C= (p.Thr574=) c.642C= (p.Thr214=) n.2739C= n.2715C= n.2703C= c.1674C= (p.Thr558=) | |
| 14 | g.78714793C>G | CA487515895 | NRXN3 | c.1698C>G (p.Thr566=) c.1710C>G (p.Thr570=) c.941C>G c.981C>G (p.Thr327=) c.579C>G (p.Thr193=) c.1692C>G (p.Thr564=) n.1042C>G n.941C>G n.2697C>G c.1734C>G (p.Thr578=) c.1722C>G (p.Thr574=) c.642C>G (p.Thr214=) n.2739C>G n.2715C>G n.2703C>G c.1674C>G (p.Thr558=) | |
| 14 | g.78714793C>T | CA7291700 | NRXN3 | c.1698C>T (p.Thr566=) c.1710C>T (p.Thr570=) c.941C>T c.981C>T (p.Thr327=) c.579C>T (p.Thr193=) c.1692C>T (p.Thr564=) n.1042C>T n.941C>T n.2697C>T c.1734C>T (p.Thr578=) c.1722C>T (p.Thr574=) c.642C>T (p.Thr214=) n.2739C>T n.2715C>T n.2703C>T c.1674C>T (p.Thr558=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.78714794G>A | CA390755815 | NRXN3 | c.1699G>A (p.Ala567Thr) c.1711G>A (p.Ala571Thr) c.942G>A c.982G>A (p.Ala328Thr) c.580G>A (p.Ala194Thr) c.1693G>A (p.Ala565Thr) n.1043G>A n.942G>A n.2698G>A c.1735G>A (p.Ala579Thr) c.1723G>A (p.Ala575Thr) c.643G>A (p.Ala215Thr) n.2740G>A n.2716G>A n.2704G>A c.1675G>A (p.Ala559Thr) | gnomAD v4 COSMIC |
| 14 | g.78714794G>C | CA390755816 | NRXN3 | c.1699G>C (p.Ala567Pro) c.1711G>C (p.Ala571Pro) c.942G>C c.982G>C (p.Ala328Pro) c.580G>C (p.Ala194Pro) c.1693G>C (p.Ala565Pro) n.1043G>C n.942G>C n.2698G>C c.1735G>C (p.Ala579Pro) c.1723G>C (p.Ala575Pro) c.643G>C (p.Ala215Pro) n.2740G>C n.2716G>C n.2704G>C c.1675G>C (p.Ala559Pro) | dbSNP |
| 14 | g.78714794G= | CA2148986584 | NRXN3 | c.1699G= (p.Ala567=) c.1711G= (p.Ala571=) c.942G= c.982G= (p.Ala328=) c.580G= (p.Ala194=) c.1693G= (p.Ala565=) n.1043G= n.942G= n.2698G= c.1735G= (p.Ala579=) c.1723G= (p.Ala575=) c.643G= (p.Ala215=) n.2740G= n.2716G= n.2704G= c.1675G= (p.Ala559=) | |
| 14 | g.78714794G>T | CA390755817 | NRXN3 | c.1699G>T (p.Ala567Ser) c.1711G>T (p.Ala571Ser) c.942G>T c.982G>T (p.Ala328Ser) c.580G>T (p.Ala194Ser) c.1693G>T (p.Ala565Ser) n.1043G>T n.942G>T n.2698G>T c.1735G>T (p.Ala579Ser) c.1723G>T (p.Ala575Ser) c.643G>T (p.Ala215Ser) n.2740G>T n.2716G>T n.2704G>T c.1675G>T (p.Ala559Ser) | |
| 14 | g.78714795C>A | CA390755818 | NRXN3 | c.1700C>A (p.Ala567Asp) c.1712C>A (p.Ala571Asp) c.943C>A c.983C>A (p.Ala328Asp) c.581C>A (p.Ala194Asp) c.1694C>A (p.Ala565Asp) n.1044C>A n.943C>A n.2699C>A c.1736C>A (p.Ala579Asp) c.1724C>A (p.Ala575Asp) c.644C>A (p.Ala215Asp) n.2741C>A n.2717C>A n.2705C>A c.1676C>A (p.Ala559Asp) | |
| 14 | g.78714795C= | CA2148986585 | NRXN3 | c.1700C= (p.Ala567=) c.1712C= (p.Ala571=) c.943C= c.983C= (p.Ala328=) c.581C= (p.Ala194=) c.1694C= (p.Ala565=) n.1044C= n.943C= n.2699C= c.1736C= (p.Ala579=) c.1724C= (p.Ala575=) c.644C= (p.Ala215=) n.2741C= n.2717C= n.2705C= c.1676C= (p.Ala559=) | |
| 14 | g.78714795C>G | CA390755819 | NRXN3 | c.1700C>G (p.Ala567Gly) c.1712C>G (p.Ala571Gly) c.943C>G c.983C>G (p.Ala328Gly) c.581C>G (p.Ala194Gly) c.1694C>G (p.Ala565Gly) n.1044C>G n.943C>G n.2699C>G c.1736C>G (p.Ala579Gly) c.1724C>G (p.Ala575Gly) c.644C>G (p.Ala215Gly) n.2741C>G n.2717C>G n.2705C>G c.1676C>G (p.Ala559Gly) | |
| 14 | g.78714795C>T | CA390755820 | NRXN3 | c.1700C>T (p.Ala567Val) c.1712C>T (p.Ala571Val) c.943C>T c.983C>T (p.Ala328Val) c.581C>T (p.Ala194Val) c.1694C>T (p.Ala565Val) n.1044C>T n.943C>T n.2699C>T c.1736C>T (p.Ala579Val) c.1724C>T (p.Ala575Val) c.644C>T (p.Ala215Val) n.2741C>T n.2717C>T n.2705C>T c.1676C>T (p.Ala559Val) | dbSNP |
| 14 | g.78714796C>A | CA487515897 | NRXN3 | c.1701C>A (p.Ala567=) c.1713C>A (p.Ala571=) c.944C>A c.984C>A (p.Ala328=) c.582C>A (p.Ala194=) c.1695C>A (p.Ala565=) n.1045C>A n.944C>A n.2700C>A c.1737C>A (p.Ala579=) c.1725C>A (p.Ala575=) c.645C>A (p.Ala215=) n.2742C>A n.2718C>A n.2706C>A c.1677C>A (p.Ala559=) | |
| 14 | g.78714796C= | CA2148986586 | NRXN3 | c.1701C= (p.Ala567=) c.1713C= (p.Ala571=) c.944C= c.984C= (p.Ala328=) c.582C= (p.Ala194=) c.1695C= (p.Ala565=) n.1045C= n.944C= n.2700C= c.1737C= (p.Ala579=) c.1725C= (p.Ala575=) c.645C= (p.Ala215=) n.2742C= n.2718C= n.2706C= c.1677C= (p.Ala559=) | |
| 14 | g.78714796C>G | CA487515898 | NRXN3 | c.1701C>G (p.Ala567=) c.1713C>G (p.Ala571=) c.944C>G c.984C>G (p.Ala328=) c.582C>G (p.Ala194=) c.1695C>G (p.Ala565=) n.1045C>G n.944C>G n.2700C>G c.1737C>G (p.Ala579=) c.1725C>G (p.Ala575=) c.645C>G (p.Ala215=) n.2742C>G n.2718C>G n.2706C>G c.1677C>G (p.Ala559=) |