Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.46032126G>A | CA8618404 | KANSL1 | c.3011C>T (p.Pro1004Leu) c.3008C>T (p.Pro1003Leu) c.2819C>T (p.Pro940Leu) c.668C>T (p.Pro223Leu) n.428C>T c.2879C>T (p.Pro960Leu) n.7228C>T n.441C>T n.983C>T c.2909C>T (p.Pro970Leu) c.2822C>T (p.Pro941Leu) c.1781C>T (p.Pro594Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.46032126G>C | CA399986548 | KANSL1 | c.3011C>G (p.Pro1004Arg) c.3008C>G (p.Pro1003Arg) c.2819C>G (p.Pro940Arg) c.668C>G (p.Pro223Arg) n.428C>G c.2879C>G (p.Pro960Arg) n.7228C>G n.441C>G n.983C>G c.2909C>G (p.Pro970Arg) c.2822C>G (p.Pro941Arg) c.1781C>G (p.Pro594Arg) | |
17 | g.46032126G= | CA2262111014 | KANSL1 | c.3011C= (p.Pro1004=) c.3008C= (p.Pro1003=) c.2819C= (p.Pro940=) c.668C= (p.Pro223=) n.428C= c.2879C= (p.Pro960=) n.7228C= n.441C= n.983C= c.2909C= (p.Pro970=) c.2822C= (p.Pro941=) c.1781C= (p.Pro594=) | |
17 | g.46032126G>T | CA399986550 | KANSL1 | c.3011C>A (p.Pro1004His) c.3008C>A (p.Pro1003His) c.2819C>A (p.Pro940His) c.668C>A (p.Pro223His) n.428C>A c.2879C>A (p.Pro960His) n.7228C>A n.441C>A n.983C>A c.2909C>A (p.Pro970His) c.2822C>A (p.Pro941His) c.1781C>A (p.Pro594His) | |
17 | g.46032129del | CA2573054461 | KANSL1 | c.3011del (p.Pro1004LeufsTer10) c.3008del (p.Pro1003LeufsTer10) c.2819del (p.Pro940LeufsTer10) c.668del (p.Pro223LeufsTer?) n.428del c.2879del (p.Pro960LeufsTer10) n.7228del n.441del n.983del c.2909del (p.Pro970LeufsTer10) c.2822del (p.Pro941LeufsTer10) c.1781del (p.Pro594LeufsTer10) | ClinVar dbSNP |
17 | g.46032127_46032136del | CA2638372199 | KANSL1 | c.3002_3011del (p.Pro1001LeufsTer10) c.2999_3008del (p.Pro1000LeufsTer10) c.2810_2819del (p.Pro937LeufsTer10) c.659_668del (p.Pro220LeufsTer?) n.419_428del c.2870_2879del (p.Pro957LeufsTer10) n.7219_7228del n.432_441del n.974_983del c.2900_2909del (p.Pro967LeufsTer10) c.2813_2822del (p.Pro938LeufsTer10) c.1772_1781del (p.Pro591LeufsTer10) | gnomAD v4 |
17 | g.46032127G>A | CA399986554 | KANSL1 | c.3010C>T (p.Pro1004Ser) c.3007C>T (p.Pro1003Ser) c.2818C>T (p.Pro940Ser) c.667C>T (p.Pro223Ser) n.427C>T c.2878C>T (p.Pro960Ser) n.7227C>T n.440C>T n.982C>T c.2908C>T (p.Pro970Ser) c.2821C>T (p.Pro941Ser) c.1780C>T (p.Pro594Ser) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.46032127G>C | CA399986558 | KANSL1 | c.3010C>G (p.Pro1004Ala) c.3007C>G (p.Pro1003Ala) c.2818C>G (p.Pro940Ala) c.667C>G (p.Pro223Ala) n.427C>G c.2878C>G (p.Pro960Ala) n.7227C>G n.440C>G n.982C>G c.2908C>G (p.Pro970Ala) c.2821C>G (p.Pro941Ala) c.1780C>G (p.Pro594Ala) | |
17 | g.46032127G= | CA2262111015 | KANSL1 | c.3010C= (p.Pro1004=) c.3007C= (p.Pro1003=) c.2818C= (p.Pro940=) c.667C= (p.Pro223=) n.427C= c.2878C= (p.Pro960=) n.7227C= n.440C= n.982C= c.2908C= (p.Pro970=) c.2821C= (p.Pro941=) c.1780C= (p.Pro594=) | |
17 | g.46032127G>T | CA399986561 | KANSL1 | c.3010C>A (p.Pro1004Thr) c.3007C>A (p.Pro1003Thr) c.2818C>A (p.Pro940Thr) c.667C>A (p.Pro223Thr) n.427C>A c.2878C>A (p.Pro960Thr) n.7227C>A n.440C>A n.982C>A c.2908C>A (p.Pro970Thr) c.2821C>A (p.Pro941Thr) c.1780C>A (p.Pro594Thr) | |
17 | g.46032128G>A | CA500371969 | KANSL1 | c.3009C>T (p.Thr1003=) c.3006C>T (p.Thr1002=) c.2817C>T (p.Thr939=) c.666C>T (p.Thr222=) n.426C>T c.2877C>T (p.Thr959=) n.7226C>T n.439C>T n.981C>T c.2907C>T (p.Thr969=) c.2820C>T (p.Thr940=) c.1779C>T (p.Thr593=) | |
17 | g.46032128G>C | CA500371968 | KANSL1 | c.3009C>G (p.Thr1003=) c.3006C>G (p.Thr1002=) c.2817C>G (p.Thr939=) c.666C>G (p.Thr222=) n.426C>G c.2877C>G (p.Thr959=) n.7226C>G n.439C>G n.981C>G c.2907C>G (p.Thr969=) c.2820C>G (p.Thr940=) c.1779C>G (p.Thr593=) | |
17 | g.46032128G>T | CA500371970 | KANSL1 | c.3009C>A (p.Thr1003=) c.3006C>A (p.Thr1002=) c.2817C>A (p.Thr939=) c.666C>A (p.Thr222=) n.426C>A c.2877C>A (p.Thr959=) n.7226C>A n.439C>A n.981C>A c.2907C>A (p.Thr969=) c.2820C>A (p.Thr940=) c.1779C>A (p.Thr593=) | |
17 | g.46032129G>A | CA16608481 | KANSL1 | c.3008C>T (p.Thr1003Ile) c.3005C>T (p.Thr1002Ile) c.2816C>T (p.Thr939Ile) c.665C>T (p.Thr222Ile) n.425C>T c.2876C>T (p.Thr959Ile) n.7225C>T n.438C>T n.980C>T c.2906C>T (p.Thr969Ile) c.2819C>T (p.Thr940Ile) c.1778C>T (p.Thr593Ile) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.46032129G>C | CA8618405 | KANSL1 | c.3008C>G (p.Thr1003Ser) c.3005C>G (p.Thr1002Ser) c.2816C>G (p.Thr939Ser) c.665C>G (p.Thr222Ser) n.425C>G c.2876C>G (p.Thr959Ser) n.7225C>G n.438C>G n.980C>G c.2906C>G (p.Thr969Ser) c.2819C>G (p.Thr940Ser) c.1778C>G (p.Thr593Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.46032129G= | CA2262111016 | KANSL1 | c.3008C= (p.Thr1003=) c.3005C= (p.Thr1002=) c.2816C= (p.Thr939=) c.665C= (p.Thr222=) n.425C= c.2876C= (p.Thr959=) n.7225C= n.438C= n.980C= c.2906C= (p.Thr969=) c.2819C= (p.Thr940=) c.1778C= (p.Thr593=) | |
17 | g.46032129G>T | CA399986565 | KANSL1 | c.3008C>A (p.Thr1003Asn) c.3005C>A (p.Thr1002Asn) c.2816C>A (p.Thr939Asn) c.665C>A (p.Thr222Asn) n.425C>A c.2876C>A (p.Thr959Asn) n.7225C>A n.438C>A n.980C>A c.2906C>A (p.Thr969Asn) c.2819C>A (p.Thr940Asn) c.1778C>A (p.Thr593Asn) | |
17 | g.46032130T>A | CA399986569 | KANSL1 | c.3007A>T (p.Thr1003Ser) c.3004A>T (p.Thr1002Ser) c.2815A>T (p.Thr939Ser) c.664A>T (p.Thr222Ser) n.424A>T c.2875A>T (p.Thr959Ser) n.7224A>T n.437A>T n.979A>T c.2905A>T (p.Thr969Ser) c.2818A>T (p.Thr940Ser) c.1777A>T (p.Thr593Ser) | |
17 | g.46032130T>C | CA399986570 | KANSL1 | c.3007A>G (p.Thr1003Ala) c.3004A>G (p.Thr1002Ala) c.2815A>G (p.Thr939Ala) c.664A>G (p.Thr222Ala) n.424A>G c.2875A>G (p.Thr959Ala) n.7224A>G n.437A>G n.979A>G c.2905A>G (p.Thr969Ala) c.2818A>G (p.Thr940Ala) c.1777A>G (p.Thr593Ala) | |
17 | g.46032130T>G | CA399986574 | KANSL1 | c.3007A>C (p.Thr1003Pro) c.3004A>C (p.Thr1002Pro) c.2815A>C (p.Thr939Pro) c.664A>C (p.Thr222Pro) n.424A>C c.2875A>C (p.Thr959Pro) n.7224A>C n.437A>C n.979A>C c.2905A>C (p.Thr969Pro) c.2818A>C (p.Thr940Pro) c.1777A>C (p.Thr593Pro) | dbSNP |
17 | g.46032131G>A | CA500371972 | KANSL1 | c.3006C>T (p.Leu1002=) c.3003C>T (p.Leu1001=) c.2814C>T (p.Leu938=) c.663C>T (p.Leu221=) n.423C>T c.2874C>T (p.Leu958=) n.7223C>T n.436C>T n.978C>T c.2904C>T (p.Leu968=) c.2817C>T (p.Leu939=) c.1776C>T (p.Leu592=) | dbSNP gnomAD v4 COSMIC |
17 | g.46032131G>C | CA500371973 | KANSL1 | c.3006C>G (p.Leu1002=) c.3003C>G (p.Leu1001=) c.2814C>G (p.Leu938=) c.663C>G (p.Leu221=) n.423C>G c.2874C>G (p.Leu958=) n.7223C>G n.436C>G n.978C>G c.2904C>G (p.Leu968=) c.2817C>G (p.Leu939=) c.1776C>G (p.Leu592=) | |
17 | g.46032131G= | CA2262111017 | KANSL1 | c.3006C= (p.Leu1002=) c.3003C= (p.Leu1001=) c.2814C= (p.Leu938=) c.663C= (p.Leu221=) n.423C= c.2874C= (p.Leu958=) n.7223C= n.436C= n.978C= c.2904C= (p.Leu968=) c.2817C= (p.Leu939=) c.1776C= (p.Leu592=) | |
17 | g.46032131G>T | CA500371971 | KANSL1 | c.3006C>A (p.Leu1002=) c.3003C>A (p.Leu1001=) c.2814C>A (p.Leu938=) c.663C>A (p.Leu221=) n.423C>A c.2874C>A (p.Leu958=) n.7223C>A n.436C>A n.978C>A c.2904C>A (p.Leu968=) c.2817C>A (p.Leu939=) c.1776C>A (p.Leu592=) | |
17 | g.46032132A>C | CA399986577 | KANSL1 | c.3005T>G (p.Leu1002Arg) c.3002T>G (p.Leu1001Arg) c.2813T>G (p.Leu938Arg) c.662T>G (p.Leu221Arg) n.422T>G c.2873T>G (p.Leu958Arg) n.7222T>G n.435T>G n.977T>G c.2903T>G (p.Leu968Arg) c.2816T>G (p.Leu939Arg) c.1775T>G (p.Leu592Arg) | |
17 | g.46032132A>G | CA399986580 | KANSL1 | c.3005T>C (p.Leu1002Pro) c.3002T>C (p.Leu1001Pro) c.2813T>C (p.Leu938Pro) c.662T>C (p.Leu221Pro) n.422T>C c.2873T>C (p.Leu958Pro) n.7222T>C n.435T>C n.977T>C c.2903T>C (p.Leu968Pro) c.2816T>C (p.Leu939Pro) c.1775T>C (p.Leu592Pro) | |
17 | g.46032132A>T | CA399986583 | KANSL1 | c.3005T>A (p.Leu1002His) c.3002T>A (p.Leu1001His) c.2813T>A (p.Leu938His) c.662T>A (p.Leu221His) n.422T>A c.2873T>A (p.Leu958His) n.7222T>A n.435T>A n.977T>A c.2903T>A (p.Leu968His) c.2816T>A (p.Leu939His) c.1775T>A (p.Leu592His) | gnomAD v4 |
17 | g.46032133G>A | CA399986587 | KANSL1 | c.3004C>T (p.Leu1002Phe) c.3001C>T (p.Leu1001Phe) c.2812C>T (p.Leu938Phe) c.661C>T (p.Leu221Phe) n.421C>T c.2872C>T (p.Leu958Phe) n.7221C>T n.434C>T n.976C>T c.2902C>T (p.Leu968Phe) c.2815C>T (p.Leu939Phe) c.1774C>T (p.Leu592Phe) | ClinVar gnomAD v4 |
17 | g.46032133G>C | CA399986589 | KANSL1 | c.3004C>G (p.Leu1002Val) c.3001C>G (p.Leu1001Val) c.2812C>G (p.Leu938Val) c.661C>G (p.Leu221Val) n.421C>G c.2872C>G (p.Leu958Val) n.7221C>G n.434C>G n.976C>G c.2902C>G (p.Leu968Val) c.2815C>G (p.Leu939Val) c.1774C>G (p.Leu592Val) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.46032133G= | CA2262111018 | KANSL1 | c.3004C= (p.Leu1002=) c.3001C= (p.Leu1001=) c.2812C= (p.Leu938=) c.661C= (p.Leu221=) n.421C= c.2872C= (p.Leu958=) n.7221C= n.434C= n.976C= c.2902C= (p.Leu968=) c.2815C= (p.Leu939=) c.1774C= (p.Leu592=) | |
17 | g.46032133G>T | CA399986592 | KANSL1 | c.3004C>A (p.Leu1002Ile) c.3001C>A (p.Leu1001Ile) c.2812C>A (p.Leu938Ile) c.661C>A (p.Leu221Ile) n.421C>A c.2872C>A (p.Leu958Ile) n.7221C>A n.434C>A n.976C>A c.2902C>A (p.Leu968Ile) c.2815C>A (p.Leu939Ile) c.1774C>A (p.Leu592Ile) | |
17 | g.46032134G>A | CA8618406 | KANSL1 | c.3003C>T (p.Pro1001=) c.3000C>T (p.Pro1000=) c.2811C>T (p.Pro937=) c.660C>T (p.Pro220=) n.420C>T c.2871C>T (p.Pro957=) n.7220C>T n.433C>T n.975C>T c.2901C>T (p.Pro967=) c.2814C>T (p.Pro938=) c.1773C>T (p.Pro591=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.46032134G>C | CA500371976 | KANSL1 | c.3003C>G (p.Pro1001=) c.3000C>G (p.Pro1000=) c.2811C>G (p.Pro937=) c.660C>G (p.Pro220=) n.420C>G c.2871C>G (p.Pro957=) n.7220C>G n.433C>G n.975C>G c.2901C>G (p.Pro967=) c.2814C>G (p.Pro938=) c.1773C>G (p.Pro591=) | |
17 | g.46032134G= | CA2262111019 | KANSL1 | c.3003C= (p.Pro1001=) c.3000C= (p.Pro1000=) c.2811C= (p.Pro937=) c.660C= (p.Pro220=) n.420C= c.2871C= (p.Pro957=) n.7220C= n.433C= n.975C= c.2901C= (p.Pro967=) c.2814C= (p.Pro938=) c.1773C= (p.Pro591=) | |
17 | g.46032134G>T | CA500371975 | KANSL1 | c.3003C>A (p.Pro1001=) c.3000C>A (p.Pro1000=) c.2811C>A (p.Pro937=) c.660C>A (p.Pro220=) n.420C>A c.2871C>A (p.Pro957=) n.7220C>A n.433C>A n.975C>A c.2901C>A (p.Pro967=) c.2814C>A (p.Pro938=) c.1773C>A (p.Pro591=) | |
17 | g.46032135G>A | CA16607657 | KANSL1 | c.3002C>T (p.Pro1001Leu) c.2999C>T (p.Pro1000Leu) c.2810C>T (p.Pro937Leu) c.659C>T (p.Pro220Leu) n.419C>T c.2870C>T (p.Pro957Leu) n.7219C>T n.432C>T n.974C>T c.2900C>T (p.Pro967Leu) c.2813C>T (p.Pro938Leu) c.1772C>T (p.Pro591Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.46032135G>C | CA399986601 | KANSL1 | c.3002C>G (p.Pro1001Arg) c.2999C>G (p.Pro1000Arg) c.2810C>G (p.Pro937Arg) c.659C>G (p.Pro220Arg) n.419C>G c.2870C>G (p.Pro957Arg) n.7219C>G n.432C>G n.974C>G c.2900C>G (p.Pro967Arg) c.2813C>G (p.Pro938Arg) c.1772C>G (p.Pro591Arg) | |
17 | g.46032135G= | CA2262111020 | KANSL1 | c.3002C= (p.Pro1001=) c.2999C= (p.Pro1000=) c.2810C= (p.Pro937=) c.659C= (p.Pro220=) n.419C= c.2870C= (p.Pro957=) n.7219C= n.432C= n.974C= c.2900C= (p.Pro967=) c.2813C= (p.Pro938=) c.1772C= (p.Pro591=) | |
17 | g.46032135G>T | CA399986599 | KANSL1 | c.3002C>A (p.Pro1001His) c.2999C>A (p.Pro1000His) c.2810C>A (p.Pro937His) c.659C>A (p.Pro220His) n.419C>A c.2870C>A (p.Pro957His) n.7219C>A n.432C>A n.974C>A c.2900C>A (p.Pro967His) c.2813C>A (p.Pro938His) c.1772C>A (p.Pro591His) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.46032136G>A | CA399986606 | KANSL1 | c.3001C>T (p.Pro1001Ser) c.2998C>T (p.Pro1000Ser) c.2809C>T (p.Pro937Ser) c.658C>T (p.Pro220Ser) n.418C>T c.2869C>T (p.Pro957Ser) n.7218C>T n.431C>T n.973C>T c.2899C>T (p.Pro967Ser) c.2812C>T (p.Pro938Ser) c.1771C>T (p.Pro591Ser) | |
17 | g.46032136G>C | CA399986608 | KANSL1 | c.3001C>G (p.Pro1001Ala) c.2998C>G (p.Pro1000Ala) c.2809C>G (p.Pro937Ala) c.658C>G (p.Pro220Ala) n.418C>G c.2869C>G (p.Pro957Ala) n.7218C>G n.431C>G n.973C>G c.2899C>G (p.Pro967Ala) c.2812C>G (p.Pro938Ala) c.1771C>G (p.Pro591Ala) | |
17 | g.46032136G>T | CA399986611 | KANSL1 | c.3001C>A (p.Pro1001Thr) c.2998C>A (p.Pro1000Thr) c.2809C>A (p.Pro937Thr) c.658C>A (p.Pro220Thr) n.418C>A c.2869C>A (p.Pro957Thr) n.7218C>A n.431C>A n.973C>A c.2899C>A (p.Pro967Thr) c.2812C>A (p.Pro938Thr) c.1771C>A (p.Pro591Thr) | |
17 | g.46032137T>A | CA500371978 | KANSL1 | c.3000A>T (p.Ala1000=) c.2997A>T (p.Ala999=) c.2808A>T (p.Ala936=) c.657A>T (p.Ala219=) n.417A>T c.2868A>T (p.Ala956=) n.7217A>T n.430A>T n.972A>T c.2898A>T (p.Ala966=) c.2811A>T (p.Ala937=) c.1770A>T (p.Ala590=) | |
17 | g.46032137T>C | CA500371979 | KANSL1 | c.3000A>G (p.Ala1000=) c.2997A>G (p.Ala999=) c.2808A>G (p.Ala936=) c.657A>G (p.Ala219=) n.417A>G c.2868A>G (p.Ala956=) n.7217A>G n.430A>G n.972A>G c.2898A>G (p.Ala966=) c.2811A>G (p.Ala937=) c.1770A>G (p.Ala590=) | |
17 | g.46032137T>G | CA500371977 | KANSL1 | c.3000A>C (p.Ala1000=) c.2997A>C (p.Ala999=) c.2808A>C (p.Ala936=) c.657A>C (p.Ala219=) n.417A>C c.2868A>C (p.Ala956=) n.7217A>C n.430A>C n.972A>C c.2898A>C (p.Ala966=) c.2811A>C (p.Ala937=) c.1770A>C (p.Ala590=) | gnomAD v3 gnomAD v4 |
17 | g.46032138G>A | CA399986614 | KANSL1 | c.2999C>T (p.Ala1000Val) c.2996C>T (p.Ala999Val) c.2807C>T (p.Ala936Val) c.656C>T (p.Ala219Val) n.416C>T c.2867C>T (p.Ala956Val) n.7216C>T n.429C>T n.971C>T c.2897C>T (p.Ala966Val) c.2810C>T (p.Ala937Val) c.1769C>T (p.Ala590Val) | |
17 | g.46032138G>C | CA399986617 | KANSL1 | c.2999C>G (p.Ala1000Gly) c.2996C>G (p.Ala999Gly) c.2807C>G (p.Ala936Gly) c.656C>G (p.Ala219Gly) n.416C>G c.2867C>G (p.Ala956Gly) n.7216C>G n.429C>G n.971C>G c.2897C>G (p.Ala966Gly) c.2810C>G (p.Ala937Gly) c.1769C>G (p.Ala590Gly) | |
17 | g.46032138G>T | CA399986619 | KANSL1 | c.2999C>A (p.Ala1000Glu) c.2996C>A (p.Ala999Glu) c.2807C>A (p.Ala936Glu) c.656C>A (p.Ala219Glu) n.416C>A c.2867C>A (p.Ala956Glu) n.7216C>A n.429C>A n.971C>A c.2897C>A (p.Ala966Glu) c.2810C>A (p.Ala937Glu) c.1769C>A (p.Ala590Glu) | |
17 | g.46032139C>A | CA399986623 | KANSL1 | c.2998G>T (p.Ala1000Ser) c.2995G>T (p.Ala999Ser) c.2806G>T (p.Ala936Ser) c.655G>T (p.Ala219Ser) n.415G>T c.2866G>T (p.Ala956Ser) n.7215G>T n.428G>T n.970G>T c.2896G>T (p.Ala966Ser) c.2809G>T (p.Ala937Ser) c.1768G>T (p.Ala590Ser) | |
17 | g.46032139C>G | CA399986625 | KANSL1 | c.2998G>C (p.Ala1000Pro) c.2995G>C (p.Ala999Pro) c.2806G>C (p.Ala936Pro) c.655G>C (p.Ala219Pro) n.415G>C c.2866G>C (p.Ala956Pro) n.7215G>C n.428G>C n.970G>C c.2896G>C (p.Ala966Pro) c.2809G>C (p.Ala937Pro) c.1768G>C (p.Ala590Pro) | |
17 | g.46032139C>T | CA399986629 | KANSL1 | c.2998G>A (p.Ala1000Thr) c.2995G>A (p.Ala999Thr) c.2806G>A (p.Ala936Thr) c.655G>A (p.Ala219Thr) n.415G>A c.2866G>A (p.Ala956Thr) n.7215G>A n.428G>A n.970G>A c.2896G>A (p.Ala966Thr) c.2809G>A (p.Ala937Thr) c.1768G>A (p.Ala590Thr) | ClinVar |
17 | g.46032140T>A | CA500371982 | KANSL1 | c.2997A>T (p.Ser999=) c.2994A>T (p.Ser998=) c.2805A>T (p.Ser935=) c.654A>T (p.Ser218=) n.414A>T c.2865A>T (p.Ser955=) n.7214A>T n.427A>T n.969A>T c.2895A>T (p.Ser965=) c.2808A>T (p.Ser936=) c.1767A>T (p.Ser589=) | |
17 | g.46032140T>C | CA500371980 | KANSL1 | c.2997A>G (p.Ser999=) c.2994A>G (p.Ser998=) c.2805A>G (p.Ser935=) c.654A>G (p.Ser218=) n.414A>G c.2865A>G (p.Ser955=) n.7214A>G n.427A>G n.969A>G c.2895A>G (p.Ser965=) c.2808A>G (p.Ser936=) c.1767A>G (p.Ser589=) | |
17 | g.46032140T>G | CA500371981 | KANSL1 | c.2997A>C (p.Ser999=) c.2994A>C (p.Ser998=) c.2805A>C (p.Ser935=) c.654A>C (p.Ser218=) n.414A>C c.2865A>C (p.Ser955=) n.7214A>C n.427A>C n.969A>C c.2895A>C (p.Ser965=) c.2808A>C (p.Ser936=) c.1767A>C (p.Ser589=) | |
17 | g.46032141G>A | CA399986632 | KANSL1 | c.2996C>T (p.Ser999Leu) c.2993C>T (p.Ser998Leu) c.2804C>T (p.Ser935Leu) c.653C>T (p.Ser218Leu) n.413C>T c.2864C>T (p.Ser955Leu) n.7213C>T n.426C>T n.968C>T c.2894C>T (p.Ser965Leu) c.2807C>T (p.Ser936Leu) c.1766C>T (p.Ser589Leu) | |
17 | g.46032141G>C | CA399986635 | KANSL1 | c.2996C>G (p.Ser999Ter) c.2993C>G (p.Ser998Ter) c.2804C>G (p.Ser935Ter) c.653C>G (p.Ser218Ter) n.413C>G c.2864C>G (p.Ser955Ter) n.7213C>G n.426C>G n.968C>G c.2894C>G (p.Ser965Ter) c.2807C>G (p.Ser936Ter) c.1766C>G (p.Ser589Ter) | COSMIC |
17 | g.46032141G>T | CA399986639 | KANSL1 | c.2996C>A (p.Ser999Ter) c.2993C>A (p.Ser998Ter) c.2804C>A (p.Ser935Ter) c.653C>A (p.Ser218Ter) n.413C>A c.2864C>A (p.Ser955Ter) n.7213C>A n.426C>A n.968C>A c.2894C>A (p.Ser965Ter) c.2807C>A (p.Ser936Ter) c.1766C>A (p.Ser589Ter) | |
17 | g.46032142A>C | CA399986649 | KANSL1 | c.2995T>G (p.Ser999Ala) c.2992T>G (p.Ser998Ala) c.2803T>G (p.Ser935Ala) c.652T>G (p.Ser218Ala) n.412T>G c.2863T>G (p.Ser955Ala) n.7212T>G n.425T>G n.967T>G c.2893T>G (p.Ser965Ala) c.2806T>G (p.Ser936Ala) c.1765T>G (p.Ser589Ala) | |
17 | g.46032142A>G | CA399986644 | KANSL1 | c.2995T>C (p.Ser999Pro) c.2992T>C (p.Ser998Pro) c.2803T>C (p.Ser935Pro) c.652T>C (p.Ser218Pro) n.412T>C c.2863T>C (p.Ser955Pro) n.7212T>C n.425T>C n.967T>C c.2893T>C (p.Ser965Pro) c.2806T>C (p.Ser936Pro) c.1765T>C (p.Ser589Pro) | gnomAD v4 |
17 | g.46032142A>T | CA399986647 | KANSL1 | c.2995T>A (p.Ser999Thr) c.2992T>A (p.Ser998Thr) c.2803T>A (p.Ser935Thr) c.652T>A (p.Ser218Thr) n.412T>A c.2863T>A (p.Ser955Thr) n.7212T>A n.425T>A n.967T>A c.2893T>A (p.Ser965Thr) c.2806T>A (p.Ser936Thr) c.1765T>A (p.Ser589Thr) | |
17 | g.46032143G>A | CA500371983 | KANSL1 | c.2994C>T (p.His998=) c.2991C>T (p.His997=) c.2802C>T (p.His934=) c.651C>T (p.His217=) n.411C>T c.2862C>T (p.His954=) n.7211C>T n.424C>T n.966C>T c.2892C>T (p.His964=) c.2805C>T (p.His935=) c.1764C>T (p.His588=) | ClinVar dbSNP |
17 | g.46032143G>C | CA399986653 | KANSL1 | c.2994C>G (p.His998Gln) c.2991C>G (p.His997Gln) c.2802C>G (p.His934Gln) c.651C>G (p.His217Gln) n.411C>G c.2862C>G (p.His954Gln) n.7211C>G n.424C>G n.966C>G c.2892C>G (p.His964Gln) c.2805C>G (p.His935Gln) c.1764C>G (p.His588Gln) | |
17 | g.46032143G= | CA2262111021 | KANSL1 | c.2994C= (p.His998=) c.2991C= (p.His997=) c.2802C= (p.His934=) c.651C= (p.His217=) n.411C= c.2862C= (p.His954=) n.7211C= n.424C= n.966C= c.2892C= (p.His964=) c.2805C= (p.His935=) c.1764C= (p.His588=) | |
17 | g.46032143G>T | CA399986656 | KANSL1 | c.2994C>A (p.His998Gln) c.2991C>A (p.His997Gln) c.2802C>A (p.His934Gln) c.651C>A (p.His217Gln) n.411C>A c.2862C>A (p.His954Gln) n.7211C>A n.424C>A n.966C>A c.2892C>A (p.His964Gln) c.2805C>A (p.His935Gln) c.1764C>A (p.His588Gln) | |
17 | g.46032144T>A | CA399986659 | KANSL1 | c.2993A>T (p.His998Leu) c.2990A>T (p.His997Leu) c.2801A>T (p.His934Leu) c.650A>T (p.His217Leu) n.410A>T c.2861A>T (p.His954Leu) n.7210A>T n.423A>T n.965A>T c.2891A>T (p.His964Leu) c.2804A>T (p.His935Leu) c.1763A>T (p.His588Leu) | |
17 | g.46032144T>C | CA399986662 | KANSL1 | c.2993A>G (p.His998Arg) c.2990A>G (p.His997Arg) c.2801A>G (p.His934Arg) c.650A>G (p.His217Arg) n.410A>G c.2861A>G (p.His954Arg) n.7210A>G n.423A>G n.965A>G c.2891A>G (p.His964Arg) c.2804A>G (p.His935Arg) c.1763A>G (p.His588Arg) | ClinVar |
17 | g.46032144T>G | CA399986664 | KANSL1 | c.2993A>C (p.His998Pro) c.2990A>C (p.His997Pro) c.2801A>C (p.His934Pro) c.650A>C (p.His217Pro) n.410A>C c.2861A>C (p.His954Pro) n.7210A>C n.423A>C n.965A>C c.2891A>C (p.His964Pro) c.2804A>C (p.His935Pro) c.1763A>C (p.His588Pro) | |
17 | g.46032145G>A | CA399986668 | KANSL1 | c.2992C>T (p.His998Tyr) c.2989C>T (p.His997Tyr) c.2800C>T (p.His934Tyr) c.649C>T (p.His217Tyr) n.409C>T c.2860C>T (p.His954Tyr) n.7209C>T n.422C>T n.964C>T c.2890C>T (p.His964Tyr) c.2803C>T (p.His935Tyr) c.1762C>T (p.His588Tyr) | dbSNP gnomAD v2 |
17 | g.46032145G>C | CA399986670 | KANSL1 | c.2992C>G (p.His998Asp) c.2989C>G (p.His997Asp) c.2800C>G (p.His934Asp) c.649C>G (p.His217Asp) n.409C>G c.2860C>G (p.His954Asp) n.7209C>G n.422C>G n.964C>G c.2890C>G (p.His964Asp) c.2803C>G (p.His935Asp) c.1762C>G (p.His588Asp) | |
17 | g.46032145G= | CA2262111022 | KANSL1 | c.2992C= (p.His998=) c.2989C= (p.His997=) c.2800C= (p.His934=) c.649C= (p.His217=) n.409C= c.2860C= (p.His954=) n.7209C= n.422C= n.964C= c.2890C= (p.His964=) c.2803C= (p.His935=) c.1762C= (p.His588=) | |
17 | g.46032145G>T | CA399986673 | KANSL1 | c.2992C>A (p.His998Asn) c.2989C>A (p.His997Asn) c.2800C>A (p.His934Asn) c.649C>A (p.His217Asn) n.409C>A c.2860C>A (p.His954Asn) n.7209C>A n.422C>A n.964C>A c.2890C>A (p.His964Asn) c.2803C>A (p.His935Asn) c.1762C>A (p.His588Asn) | |
17 | g.46032146C>A | CA500371984 | KANSL1 | c.2991G>T (p.Leu997=) c.2988G>T (p.Leu996=) c.2799G>T (p.Leu933=) c.648G>T (p.Leu216=) n.408G>T c.2859G>T (p.Leu953=) n.7208G>T n.421G>T n.963G>T c.2889G>T (p.Leu963=) c.2802G>T (p.Leu934=) c.1761G>T (p.Leu587=) | |
17 | g.46032146C= | CA2262111023 | KANSL1 | c.2991G= (p.Leu997=) c.2988G= (p.Leu996=) c.2799G= (p.Leu933=) c.648G= (p.Leu216=) n.408G= c.2859G= (p.Leu953=) n.7208G= n.421G= n.963G= c.2889G= (p.Leu963=) c.2802G= (p.Leu934=) c.1761G= (p.Leu587=) | |
17 | g.46032146C>G | CA500371985 | KANSL1 | c.2991G>C (p.Leu997=) c.2988G>C (p.Leu996=) c.2799G>C (p.Leu933=) c.648G>C (p.Leu216=) n.408G>C c.2859G>C (p.Leu953=) n.7208G>C n.421G>C n.963G>C c.2889G>C (p.Leu963=) c.2802G>C (p.Leu934=) c.1761G>C (p.Leu587=) | |
17 | g.46032146C>T | CA8618407 | KANSL1 | c.2991G>A (p.Leu997=) c.2988G>A (p.Leu996=) c.2799G>A (p.Leu933=) c.648G>A (p.Leu216=) n.408G>A c.2859G>A (p.Leu953=) n.7208G>A n.421G>A n.963G>A c.2889G>A (p.Leu963=) c.2802G>A (p.Leu934=) c.1761G>A (p.Leu587=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.46032147A>C | CA399986679 | KANSL1 | c.2990T>G (p.Leu997Arg) c.2987T>G (p.Leu996Arg) c.2798T>G (p.Leu933Arg) c.647T>G (p.Leu216Arg) n.407T>G c.2858T>G (p.Leu953Arg) n.7207T>G n.420T>G n.962T>G c.2888T>G (p.Leu963Arg) c.2801T>G (p.Leu934Arg) c.1760T>G (p.Leu587Arg) | |
17 | g.46032147A>G | CA399986681 | KANSL1 | c.2990T>C (p.Leu997Pro) c.2987T>C (p.Leu996Pro) c.2798T>C (p.Leu933Pro) c.647T>C (p.Leu216Pro) n.407T>C c.2858T>C (p.Leu953Pro) n.7207T>C n.420T>C n.962T>C c.2888T>C (p.Leu963Pro) c.2801T>C (p.Leu934Pro) c.1760T>C (p.Leu587Pro) | |
17 | g.46032147A>T | CA399986684 | KANSL1 | c.2990T>A (p.Leu997Gln) c.2987T>A (p.Leu996Gln) c.2798T>A (p.Leu933Gln) c.647T>A (p.Leu216Gln) n.407T>A c.2858T>A (p.Leu953Gln) n.7207T>A n.420T>A n.962T>A c.2888T>A (p.Leu963Gln) c.2801T>A (p.Leu934Gln) c.1760T>A (p.Leu587Gln) | |
17 | g.46032148G>A | CA500371986 | KANSL1 | c.2989C>T (p.Leu997=) c.2986C>T (p.Leu996=) c.2797C>T (p.Leu933=) c.646C>T (p.Leu216=) n.406C>T c.2857C>T (p.Leu953=) n.7206C>T n.419C>T n.961C>T c.2887C>T (p.Leu963=) c.2800C>T (p.Leu934=) c.1759C>T (p.Leu587=) | gnomAD v4 |
17 | g.46032148G>C | CA399986690 | KANSL1 | c.2989C>G (p.Leu997Val) c.2986C>G (p.Leu996Val) c.2797C>G (p.Leu933Val) c.646C>G (p.Leu216Val) n.406C>G c.2857C>G (p.Leu953Val) n.7206C>G n.419C>G n.961C>G c.2887C>G (p.Leu963Val) c.2800C>G (p.Leu934Val) c.1759C>G (p.Leu587Val) | gnomAD v4 |
17 | g.46032148G>T | CA399986688 | KANSL1 | c.2989C>A (p.Leu997Met) c.2986C>A (p.Leu996Met) c.2797C>A (p.Leu933Met) c.646C>A (p.Leu216Met) n.406C>A c.2857C>A (p.Leu953Met) n.7206C>A n.419C>A n.961C>A c.2887C>A (p.Leu963Met) c.2800C>A (p.Leu934Met) c.1759C>A (p.Leu587Met) | |
17 | g.46032149T>A | CA399986694 | KANSL1 | c.2988A>T (p.Glu996Asp) c.2985A>T (p.Glu995Asp) c.2796A>T (p.Glu932Asp) c.645A>T (p.Glu215Asp) n.405A>T c.2856A>T (p.Glu952Asp) n.7205A>T n.418A>T n.960A>T c.2886A>T (p.Glu962Asp) c.2799A>T (p.Glu933Asp) c.1758A>T (p.Glu586Asp) | |
17 | g.46032149T>C | CA500371987 | KANSL1 | c.2988A>G (p.Glu996=) c.2985A>G (p.Glu995=) c.2796A>G (p.Glu932=) c.645A>G (p.Glu215=) n.405A>G c.2856A>G (p.Glu952=) n.7205A>G n.418A>G n.960A>G c.2886A>G (p.Glu962=) c.2799A>G (p.Glu933=) c.1758A>G (p.Glu586=) | |
17 | g.46032149T>G | CA399986697 | KANSL1 | c.2988A>C (p.Glu996Asp) c.2985A>C (p.Glu995Asp) c.2796A>C (p.Glu932Asp) c.645A>C (p.Glu215Asp) n.405A>C c.2856A>C (p.Glu952Asp) n.7205A>C n.418A>C n.960A>C c.2886A>C (p.Glu962Asp) c.2799A>C (p.Glu933Asp) c.1758A>C (p.Glu586Asp) | |
17 | g.46032150T>A | CA399986701 | KANSL1 | c.2987A>T (p.Glu996Val) c.2984A>T (p.Glu995Val) c.2795A>T (p.Glu932Val) c.644A>T (p.Glu215Val) n.404A>T c.2855A>T (p.Glu952Val) n.7204A>T n.417A>T n.959A>T c.2885A>T (p.Glu962Val) c.2798A>T (p.Glu933Val) c.1757A>T (p.Glu586Val) | |
17 | g.46032150T>C | CA399986702 | KANSL1 | c.2987A>G (p.Glu996Gly) c.2984A>G (p.Glu995Gly) c.2795A>G (p.Glu932Gly) c.644A>G (p.Glu215Gly) n.404A>G c.2855A>G (p.Glu952Gly) n.7204A>G n.417A>G n.959A>G c.2885A>G (p.Glu962Gly) c.2798A>G (p.Glu933Gly) c.1757A>G (p.Glu586Gly) | |
17 | g.46032150T>G | CA399986706 | KANSL1 | c.2987A>C (p.Glu996Ala) c.2984A>C (p.Glu995Ala) c.2795A>C (p.Glu932Ala) c.644A>C (p.Glu215Ala) n.404A>C c.2855A>C (p.Glu952Ala) n.7204A>C n.417A>C n.959A>C c.2885A>C (p.Glu962Ala) c.2798A>C (p.Glu933Ala) c.1757A>C (p.Glu586Ala) | |
17 | g.46032151C>A | CA399986709 | KANSL1 | c.2986G>T (p.Glu996Ter) c.2983G>T (p.Glu995Ter) c.2794G>T (p.Glu932Ter) c.643G>T (p.Glu215Ter) n.403G>T c.2854G>T (p.Glu952Ter) n.7203G>T n.416G>T n.958G>T c.2884G>T (p.Glu962Ter) c.2797G>T (p.Glu933Ter) c.1756G>T (p.Glu586Ter) | |
17 | g.46032151C>G | CA399986711 | KANSL1 | c.2986G>C (p.Glu996Gln) c.2983G>C (p.Glu995Gln) c.2794G>C (p.Glu932Gln) c.643G>C (p.Glu215Gln) n.403G>C c.2854G>C (p.Glu952Gln) n.7203G>C n.416G>C n.958G>C c.2884G>C (p.Glu962Gln) c.2797G>C (p.Glu933Gln) c.1756G>C (p.Glu586Gln) | |
17 | g.46032151C>T | CA399986713 | KANSL1 | c.2986G>A (p.Glu996Lys) c.2983G>A (p.Glu995Lys) c.2794G>A (p.Glu932Lys) c.643G>A (p.Glu215Lys) n.403G>A c.2854G>A (p.Glu952Lys) n.7203G>A n.416G>A n.958G>A c.2884G>A (p.Glu962Lys) c.2797G>A (p.Glu933Lys) c.1756G>A (p.Glu586Lys) | |
17 | g.46032152C>A | CA500371989 | KANSL1 | c.2985G>T (p.Pro995=) c.2982G>T (p.Pro994=) c.2793G>T (p.Pro931=) c.642G>T (p.Pro214=) n.402G>T c.2853G>T (p.Pro951=) n.7202G>T n.415G>T n.957G>T c.2883G>T (p.Pro961=) c.2796G>T (p.Pro932=) c.1755G>T (p.Pro585=) | gnomAD v4 |
17 | g.46032152C= | CA2262111024 | KANSL1 | c.2985G= (p.Pro995=) c.2982G= (p.Pro994=) c.2793G= (p.Pro931=) c.642G= (p.Pro214=) n.402G= c.2853G= (p.Pro951=) n.7202G= n.415G= n.957G= c.2883G= (p.Pro961=) c.2796G= (p.Pro932=) c.1755G= (p.Pro585=) | |
17 | g.46032152C>G | CA500371990 | KANSL1 | c.2985G>C (p.Pro995=) c.2982G>C (p.Pro994=) c.2793G>C (p.Pro931=) c.642G>C (p.Pro214=) n.402G>C c.2853G>C (p.Pro951=) n.7202G>C n.415G>C n.957G>C c.2883G>C (p.Pro961=) c.2796G>C (p.Pro932=) c.1755G>C (p.Pro585=) | |
17 | g.46032152C>T | CA8618408 | KANSL1 | c.2985G>A (p.Pro995=) c.2982G>A (p.Pro994=) c.2793G>A (p.Pro931=) c.642G>A (p.Pro214=) n.402G>A c.2853G>A (p.Pro951=) n.7202G>A n.415G>A n.957G>A c.2883G>A (p.Pro961=) c.2796G>A (p.Pro932=) c.1755G>A (p.Pro585=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.46032153G>A | CA8618409 | KANSL1 | c.2984C>T (p.Pro995Leu) c.2981C>T (p.Pro994Leu) c.2792C>T (p.Pro931Leu) c.641C>T (p.Pro214Leu) n.401C>T c.2852C>T (p.Pro951Leu) n.7201C>T n.414C>T n.956C>T c.2882C>T (p.Pro961Leu) c.2795C>T (p.Pro932Leu) c.1754C>T (p.Pro585Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.46032153G>C | CA399986720 | KANSL1 | c.2984C>G (p.Pro995Arg) c.2981C>G (p.Pro994Arg) c.2792C>G (p.Pro931Arg) c.641C>G (p.Pro214Arg) n.401C>G c.2852C>G (p.Pro951Arg) n.7201C>G n.414C>G n.956C>G c.2882C>G (p.Pro961Arg) c.2795C>G (p.Pro932Arg) c.1754C>G (p.Pro585Arg) | |
17 | g.46032153G= | CA2262111025 | KANSL1 | c.2984C= (p.Pro995=) c.2981C= (p.Pro994=) c.2792C= (p.Pro931=) c.641C= (p.Pro214=) n.401C= c.2852C= (p.Pro951=) n.7201C= n.414C= n.956C= c.2882C= (p.Pro961=) c.2795C= (p.Pro932=) c.1754C= (p.Pro585=) | |
17 | g.46032153G>T | CA399986723 | KANSL1 | c.2984C>A (p.Pro995Gln) c.2981C>A (p.Pro994Gln) c.2792C>A (p.Pro931Gln) c.641C>A (p.Pro214Gln) n.401C>A c.2852C>A (p.Pro951Gln) n.7201C>A n.414C>A n.956C>A c.2882C>A (p.Pro961Gln) c.2795C>A (p.Pro932Gln) c.1754C>A (p.Pro585Gln) | |
17 | g.46032154G>A | CA399986726 | KANSL1 | c.2983C>T (p.Pro995Ser) c.2980C>T (p.Pro994Ser) c.2791C>T (p.Pro931Ser) c.640C>T (p.Pro214Ser) n.400C>T c.2851C>T (p.Pro951Ser) n.7200C>T n.413C>T n.955C>T c.2881C>T (p.Pro961Ser) c.2794C>T (p.Pro932Ser) c.1753C>T (p.Pro585Ser) | |
17 | g.46032154G>C | CA399986727 | KANSL1 | c.2983C>G (p.Pro995Ala) c.2980C>G (p.Pro994Ala) c.2791C>G (p.Pro931Ala) c.640C>G (p.Pro214Ala) n.400C>G c.2851C>G (p.Pro951Ala) n.7200C>G n.413C>G n.955C>G c.2881C>G (p.Pro961Ala) c.2794C>G (p.Pro932Ala) c.1753C>G (p.Pro585Ala) | |
17 | g.46032154G>T | CA399986729 | KANSL1 | c.2983C>A (p.Pro995Thr) c.2980C>A (p.Pro994Thr) c.2791C>A (p.Pro931Thr) c.640C>A (p.Pro214Thr) n.400C>A c.2851C>A (p.Pro951Thr) n.7200C>A n.413C>A n.955C>A c.2881C>A (p.Pro961Thr) c.2794C>A (p.Pro932Thr) c.1753C>A (p.Pro585Thr) | |
17 | g.46032155G>A | CA500371991 | KANSL1 | c.2982C>T (p.Ser994=) c.2979C>T (p.Ser993=) c.2790C>T (p.Ser930=) c.639C>T (p.Ser213=) n.399C>T c.2850C>T (p.Ser950=) n.7199C>T n.412C>T n.954C>T c.2880C>T (p.Ser960=) c.2793C>T (p.Ser931=) c.1752C>T (p.Ser584=) | |
17 | g.46032155G>C | CA399986733 | KANSL1 | c.2982C>G (p.Ser994Arg) c.2979C>G (p.Ser993Arg) c.2790C>G (p.Ser930Arg) c.639C>G (p.Ser213Arg) n.399C>G c.2850C>G (p.Ser950Arg) n.7199C>G n.412C>G n.954C>G c.2880C>G (p.Ser960Arg) c.2793C>G (p.Ser931Arg) c.1752C>G (p.Ser584Arg) | |
17 | g.46032155G>T | CA399986736 | KANSL1 | c.2982C>A (p.Ser994Arg) c.2979C>A (p.Ser993Arg) c.2790C>A (p.Ser930Arg) c.639C>A (p.Ser213Arg) n.399C>A c.2850C>A (p.Ser950Arg) n.7199C>A n.412C>A n.954C>A c.2880C>A (p.Ser960Arg) c.2793C>A (p.Ser931Arg) c.1752C>A (p.Ser584Arg) | |
17 | g.46032156C>A | CA399986740 | KANSL1 | c.2981G>T (p.Ser994Ile) c.2978G>T (p.Ser993Ile) c.2789G>T (p.Ser930Ile) c.638G>T (p.Ser213Ile) n.398G>T c.2849G>T (p.Ser950Ile) n.7198G>T n.411G>T n.953G>T c.2879G>T (p.Ser960Ile) c.2792G>T (p.Ser931Ile) c.1751G>T (p.Ser584Ile) | ClinVar dbSNP gnomAD v4 |
17 | g.46032156C>G | CA399986743 | KANSL1 | c.2981G>C (p.Ser994Thr) c.2978G>C (p.Ser993Thr) c.2789G>C (p.Ser930Thr) c.638G>C (p.Ser213Thr) n.398G>C c.2849G>C (p.Ser950Thr) n.7198G>C n.411G>C n.953G>C c.2879G>C (p.Ser960Thr) c.2792G>C (p.Ser931Thr) c.1751G>C (p.Ser584Thr) | |
17 | g.46032156C>T | CA399986746 | KANSL1 | c.2981G>A (p.Ser994Asn) c.2978G>A (p.Ser993Asn) c.2789G>A (p.Ser930Asn) c.638G>A (p.Ser213Asn) n.398G>A c.2849G>A (p.Ser950Asn) n.7198G>A n.411G>A n.953G>A c.2879G>A (p.Ser960Asn) c.2792G>A (p.Ser931Asn) c.1751G>A (p.Ser584Asn) | |
17 | g.46032157T>A | CA399986749 | KANSL1 | c.2980A>T (p.Ser994Cys) c.2977A>T (p.Ser993Cys) c.2788A>T (p.Ser930Cys) c.637A>T (p.Ser213Cys) n.397A>T c.2848A>T (p.Ser950Cys) n.7197A>T n.410A>T n.952A>T c.2878A>T (p.Ser960Cys) c.2791A>T (p.Ser931Cys) c.1750A>T (p.Ser584Cys) | |
17 | g.46032157T>C | CA399986751 | KANSL1 | c.2980A>G (p.Ser994Gly) c.2977A>G (p.Ser993Gly) c.2788A>G (p.Ser930Gly) c.637A>G (p.Ser213Gly) n.397A>G c.2848A>G (p.Ser950Gly) n.7197A>G n.410A>G n.952A>G c.2878A>G (p.Ser960Gly) c.2791A>G (p.Ser931Gly) c.1750A>G (p.Ser584Gly) | ClinVar gnomAD v4 |
17 | g.46032157T>G | CA399986754 | KANSL1 | c.2980A>C (p.Ser994Arg) c.2977A>C (p.Ser993Arg) c.2788A>C (p.Ser930Arg) c.637A>C (p.Ser213Arg) n.397A>C c.2848A>C (p.Ser950Arg) n.7197A>C n.410A>C n.952A>C c.2878A>C (p.Ser960Arg) c.2791A>C (p.Ser931Arg) c.1750A>C (p.Ser584Arg) | |
17 | g.46032158A>C | CA399986758 | KANSL1 | c.2979T>G (p.Ile993Met) c.2976T>G (p.Ile992Met) c.2787T>G (p.Ile929Met) c.636T>G (p.Ile212Met) n.396T>G c.2847T>G (p.Ile949Met) n.7196T>G n.409T>G n.951T>G c.2877T>G (p.Ile959Met) c.2790T>G (p.Ile930Met) c.1749T>G (p.Ile583Met) | |
17 | g.46032158A>G | CA500371992 | KANSL1 | c.2979T>C (p.Ile993=) c.2976T>C (p.Ile992=) c.2787T>C (p.Ile929=) c.636T>C (p.Ile212=) n.396T>C c.2847T>C (p.Ile949=) n.7196T>C n.409T>C n.951T>C c.2877T>C (p.Ile959=) c.2790T>C (p.Ile930=) c.1749T>C (p.Ile583=) | gnomAD v4 |
17 | g.46032158A>T | CA500371993 | KANSL1 | c.2979T>A (p.Ile993=) c.2976T>A (p.Ile992=) c.2787T>A (p.Ile929=) c.636T>A (p.Ile212=) n.396T>A c.2847T>A (p.Ile949=) n.7196T>A n.409T>A n.951T>A c.2877T>A (p.Ile959=) c.2790T>A (p.Ile930=) c.1749T>A (p.Ile583=) | |
17 | g.46032159A>C | CA399986762 | KANSL1 | c.2978T>G (p.Ile993Ser) c.2975T>G (p.Ile992Ser) c.2786T>G (p.Ile929Ser) c.635T>G (p.Ile212Ser) n.395T>G c.2846T>G (p.Ile949Ser) n.7195T>G n.408T>G n.950T>G c.2876T>G (p.Ile959Ser) c.2789T>G (p.Ile930Ser) c.1748T>G (p.Ile583Ser) | |
17 | g.46032159A>G | CA399986764 | KANSL1 | c.2978T>C (p.Ile993Thr) c.2975T>C (p.Ile992Thr) c.2786T>C (p.Ile929Thr) c.635T>C (p.Ile212Thr) n.395T>C c.2846T>C (p.Ile949Thr) n.7195T>C n.408T>C n.950T>C c.2876T>C (p.Ile959Thr) c.2789T>C (p.Ile930Thr) c.1748T>C (p.Ile583Thr) | |
17 | g.46032159A>T | CA399986767 | KANSL1 | c.2978T>A (p.Ile993Asn) c.2975T>A (p.Ile992Asn) c.2786T>A (p.Ile929Asn) c.635T>A (p.Ile212Asn) n.395T>A c.2846T>A (p.Ile949Asn) n.7195T>A n.408T>A n.950T>A c.2876T>A (p.Ile959Asn) c.2789T>A (p.Ile930Asn) c.1748T>A (p.Ile583Asn) | |
17 | g.46032160T>A | CA399986770 | KANSL1 | c.2977A>T (p.Ile993Phe) c.2974A>T (p.Ile992Phe) c.2785A>T (p.Ile929Phe) c.634A>T (p.Ile212Phe) n.394A>T c.2845A>T (p.Ile949Phe) n.7194A>T n.407A>T n.949A>T c.2875A>T (p.Ile959Phe) c.2788A>T (p.Ile930Phe) c.1747A>T (p.Ile583Phe) | |
17 | g.46032160T>C | CA399986772 | KANSL1 | c.2977A>G (p.Ile993Val) c.2974A>G (p.Ile992Val) c.2785A>G (p.Ile929Val) c.634A>G (p.Ile212Val) n.394A>G c.2845A>G (p.Ile949Val) n.7194A>G n.407A>G n.949A>G c.2875A>G (p.Ile959Val) c.2788A>G (p.Ile930Val) c.1747A>G (p.Ile583Val) | |
17 | g.46032160T>G | CA399986774 | KANSL1 | c.2977A>C (p.Ile993Leu) c.2974A>C (p.Ile992Leu) c.2785A>C (p.Ile929Leu) c.634A>C (p.Ile212Leu) n.394A>C c.2845A>C (p.Ile949Leu) n.7194A>C n.407A>C n.949A>C c.2875A>C (p.Ile959Leu) c.2788A>C (p.Ile930Leu) c.1747A>C (p.Ile583Leu) | |
17 | g.46032161G>A | CA500371994 | KANSL1 | c.2976C>T (p.Pro992=) c.2973C>T (p.Pro991=) c.2784C>T (p.Pro928=) c.633C>T (p.Pro211=) n.393C>T c.2844C>T (p.Pro948=) n.7193C>T n.406C>T n.948C>T c.2874C>T (p.Pro958=) c.2787C>T (p.Pro929=) c.1746C>T (p.Pro582=) | |
17 | g.46032161G>C | CA500371995 | KANSL1 | c.2976C>G (p.Pro992=) c.2973C>G (p.Pro991=) c.2784C>G (p.Pro928=) c.633C>G (p.Pro211=) n.393C>G c.2844C>G (p.Pro948=) n.7193C>G n.406C>G n.948C>G c.2874C>G (p.Pro958=) c.2787C>G (p.Pro929=) c.1746C>G (p.Pro582=) | gnomAD v4 |
17 | g.46032161G>T | CA500371996 | KANSL1 | c.2976C>A (p.Pro992=) c.2973C>A (p.Pro991=) c.2784C>A (p.Pro928=) c.633C>A (p.Pro211=) n.393C>A c.2844C>A (p.Pro948=) n.7193C>A n.406C>A n.948C>A c.2874C>A (p.Pro958=) c.2787C>A (p.Pro929=) c.1746C>A (p.Pro582=) | |
17 | g.46032164dup | CA2841630697 | KANSL1 | c.2976dup (p.Ile993HisfsTer2) c.2973dup (p.Ile992HisfsTer2) c.2784dup (p.Ile929HisfsTer2) c.633dup (p.Ile212HisfsTer2) n.393dup c.2844dup (p.Ile949HisfsTer2) n.7193dup n.406dup n.948dup c.2874dup (p.Ile959HisfsTer2) c.2787dup (p.Ile930HisfsTer2) c.1746dup (p.Ile583HisfsTer2) | |
17 | g.46032162G>A | CA399986777 | KANSL1 | c.2975C>T (p.Pro992Leu) c.2972C>T (p.Pro991Leu) c.2783C>T (p.Pro928Leu) c.632C>T (p.Pro211Leu) n.392C>T c.2843C>T (p.Pro948Leu) n.7192C>T n.405C>T n.947C>T c.2873C>T (p.Pro958Leu) c.2786C>T (p.Pro929Leu) c.1745C>T (p.Pro582Leu) | |
17 | g.46032162G>C | CA399986781 | KANSL1 | c.2975C>G (p.Pro992Arg) c.2972C>G (p.Pro991Arg) c.2783C>G (p.Pro928Arg) c.632C>G (p.Pro211Arg) n.392C>G c.2843C>G (p.Pro948Arg) n.7192C>G n.405C>G n.947C>G c.2873C>G (p.Pro958Arg) c.2786C>G (p.Pro929Arg) c.1745C>G (p.Pro582Arg) | |
17 | g.46032162G>T | CA399986778 | KANSL1 | c.2975C>A (p.Pro992His) c.2972C>A (p.Pro991His) c.2783C>A (p.Pro928His) c.632C>A (p.Pro211His) n.392C>A c.2843C>A (p.Pro948His) n.7192C>A n.405C>A n.947C>A c.2873C>A (p.Pro958His) c.2786C>A (p.Pro929His) c.1745C>A (p.Pro582His) | |
17 | g.46032163G>A | CA399986784 | KANSL1 | c.2974C>T (p.Pro992Ser) c.2971C>T (p.Pro991Ser) c.2782C>T (p.Pro928Ser) c.631C>T (p.Pro211Ser) n.391C>T c.2842C>T (p.Pro948Ser) n.7191C>T n.404C>T n.946C>T c.2872C>T (p.Pro958Ser) c.2785C>T (p.Pro929Ser) c.1744C>T (p.Pro582Ser) | dbSNP |
17 | g.46032163G>C | CA399986786 | KANSL1 | c.2974C>G (p.Pro992Ala) c.2971C>G (p.Pro991Ala) c.2782C>G (p.Pro928Ala) c.631C>G (p.Pro211Ala) n.391C>G c.2842C>G (p.Pro948Ala) n.7191C>G n.404C>G n.946C>G c.2872C>G (p.Pro958Ala) c.2785C>G (p.Pro929Ala) c.1744C>G (p.Pro582Ala) | |
17 | g.46032163G= | CA2262111026 | KANSL1 | c.2974C= (p.Pro992=) c.2971C= (p.Pro991=) c.2782C= (p.Pro928=) c.631C= (p.Pro211=) n.391C= c.2842C= (p.Pro948=) n.7191C= n.404C= n.946C= c.2872C= (p.Pro958=) c.2785C= (p.Pro929=) c.1744C= (p.Pro582=) | |
17 | g.46032163G>T | CA399986789 | KANSL1 | c.2974C>A (p.Pro992Thr) c.2971C>A (p.Pro991Thr) c.2782C>A (p.Pro928Thr) c.631C>A (p.Pro211Thr) n.391C>A c.2842C>A (p.Pro948Thr) n.7191C>A n.404C>A n.946C>A c.2872C>A (p.Pro958Thr) c.2785C>A (p.Pro929Thr) c.1744C>A (p.Pro582Thr) | |
17 | g.46032164G>A | CA500371997 | KANSL1 | c.2973C>T (p.Ser991=) c.2970C>T (p.Ser990=) c.2781C>T (p.Ser927=) c.630C>T (p.Ser210=) n.390C>T c.2841C>T (p.Ser947=) n.7190C>T n.403C>T n.945C>T c.2871C>T (p.Ser957=) c.2784C>T (p.Ser928=) c.1743C>T (p.Ser581=) | |
17 | g.46032164G>C | CA399986793 | KANSL1 | c.2973C>G (p.Ser991Arg) c.2970C>G (p.Ser990Arg) c.2781C>G (p.Ser927Arg) c.630C>G (p.Ser210Arg) n.390C>G c.2841C>G (p.Ser947Arg) n.7190C>G n.403C>G n.945C>G c.2871C>G (p.Ser957Arg) c.2784C>G (p.Ser928Arg) c.1743C>G (p.Ser581Arg) | |
17 | g.46032164G>T | CA399986796 | KANSL1 | c.2973C>A (p.Ser991Arg) c.2970C>A (p.Ser990Arg) c.2781C>A (p.Ser927Arg) c.630C>A (p.Ser210Arg) n.390C>A c.2841C>A (p.Ser947Arg) n.7190C>A n.403C>A n.945C>A c.2871C>A (p.Ser957Arg) c.2784C>A (p.Ser928Arg) c.1743C>A (p.Ser581Arg) | |
17 | g.46032165C>A | CA399986800 | KANSL1 | c.2972G>T (p.Ser991Ile) c.2969G>T (p.Ser990Ile) c.2780G>T (p.Ser927Ile) c.629G>T (p.Ser210Ile) n.389G>T c.2840G>T (p.Ser947Ile) n.7189G>T n.358G>T n.402G>T n.944G>T c.2870G>T (p.Ser957Ile) c.2783G>T (p.Ser928Ile) c.1742G>T (p.Ser581Ile) | |
17 | g.46032165C>G | CA399986801 | KANSL1 | c.2972G>C (p.Ser991Thr) c.2969G>C (p.Ser990Thr) c.2780G>C (p.Ser927Thr) c.629G>C (p.Ser210Thr) n.389G>C c.2840G>C (p.Ser947Thr) n.7189G>C n.358G>C n.402G>C n.944G>C c.2870G>C (p.Ser957Thr) c.2783G>C (p.Ser928Thr) c.1742G>C (p.Ser581Thr) | |
17 | g.46032165C>T | CA399986805 | KANSL1 | c.2972G>A (p.Ser991Asn) c.2969G>A (p.Ser990Asn) c.2780G>A (p.Ser927Asn) c.629G>A (p.Ser210Asn) n.389G>A c.2840G>A (p.Ser947Asn) n.7189G>A n.358G>A n.402G>A n.944G>A c.2870G>A (p.Ser957Asn) c.2783G>A (p.Ser928Asn) c.1742G>A (p.Ser581Asn) | |
17 | g.46032166T>A | CA399986808 | KANSL1 | c.2971A>T (p.Ser991Cys) c.2968A>T (p.Ser990Cys) c.2779A>T (p.Ser927Cys) c.628A>T (p.Ser210Cys) n.388A>T c.2839A>T (p.Ser947Cys) n.7188A>T n.357A>T n.401A>T n.943A>T c.2869A>T (p.Ser957Cys) c.2782A>T (p.Ser928Cys) c.1741A>T (p.Ser581Cys) | |
17 | g.46032166T>C | CA399986810 | KANSL1 | c.2971A>G (p.Ser991Gly) c.2968A>G (p.Ser990Gly) c.2779A>G (p.Ser927Gly) c.628A>G (p.Ser210Gly) n.388A>G c.2839A>G (p.Ser947Gly) n.7188A>G n.357A>G n.401A>G n.943A>G c.2869A>G (p.Ser957Gly) c.2782A>G (p.Ser928Gly) c.1741A>G (p.Ser581Gly) | |
17 | g.46032166T>G | CA399986813 | KANSL1 | c.2971A>C (p.Ser991Arg) c.2968A>C (p.Ser990Arg) c.2779A>C (p.Ser927Arg) c.628A>C (p.Ser210Arg) n.388A>C c.2839A>C (p.Ser947Arg) n.7188A>C n.357A>C n.401A>C n.943A>C c.2869A>C (p.Ser957Arg) c.2782A>C (p.Ser928Arg) c.1741A>C (p.Ser581Arg) | |
17 | g.46032167C>A | CA399986816 | KANSL1 | c.2970G>T (p.Arg990Ser) c.2967G>T (p.Arg989Ser) c.2778G>T (p.Arg926Ser) c.627G>T (p.Arg209Ser) n.387G>T c.2838G>T (p.Arg946Ser) n.7187G>T n.356G>T n.400G>T n.942G>T c.2868G>T (p.Arg956Ser) c.2781G>T (p.Arg927Ser) c.1740G>T (p.Arg580Ser) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.46032167C= | CA2262111027 | KANSL1 | c.2970G= (p.Arg990=) c.2967G= (p.Arg989=) c.2778G= (p.Arg926=) c.627G= (p.Arg209=) n.387G= c.2838G= (p.Arg946=) n.7187G= n.356G= n.400G= n.942G= c.2868G= (p.Arg956=) c.2781G= (p.Arg927=) c.1740G= (p.Arg580=) | |
17 | g.46032167C>G | CA399986817 | KANSL1 | c.2970G>C (p.Arg990Ser) c.2967G>C (p.Arg989Ser) c.2778G>C (p.Arg926Ser) c.627G>C (p.Arg209Ser) n.387G>C c.2838G>C (p.Arg946Ser) n.7187G>C n.356G>C n.400G>C n.942G>C c.2868G>C (p.Arg956Ser) c.2781G>C (p.Arg927Ser) c.1740G>C (p.Arg580Ser) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.46032167C>T | CA500371998 | KANSL1 | c.2970G>A (p.Arg990=) c.2967G>A (p.Arg989=) c.2778G>A (p.Arg926=) c.627G>A (p.Arg209=) n.387G>A c.2838G>A (p.Arg946=) n.7187G>A n.356G>A n.400G>A n.942G>A c.2868G>A (p.Arg956=) c.2781G>A (p.Arg927=) c.1740G>A (p.Arg580=) | |
17 | g.46032168C>A | CA399986827 | KANSL1 | c.2969G>T (p.Arg990Met) c.2966G>T (p.Arg989Met) c.2777G>T (p.Arg926Met) c.626G>T (p.Arg209Met) n.386G>T c.2838-1G>T (n.2838-1G>T) n.7186G>T n.355G>T n.399G>T n.941G>T c.2867G>T (p.Arg956Met) c.2780G>T (p.Arg927Met) c.1739G>T (p.Arg580Met) | |
17 | g.46032168C>G | CA399986820 | KANSL1 | c.2969G>C (p.Arg990Thr) c.2966G>C (p.Arg989Thr) c.2777G>C (p.Arg926Thr) c.626G>C (p.Arg209Thr) n.386G>C c.2838-1G>C (n.2838-1G>C) n.7186G>C n.355G>C n.399G>C n.941G>C c.2867G>C (p.Arg956Thr) c.2780G>C (p.Arg927Thr) c.1739G>C (p.Arg580Thr) | |
17 | g.46032168C>T | CA399986824 | KANSL1 | c.2969G>A (p.Arg990Lys) c.2966G>A (p.Arg989Lys) c.2777G>A (p.Arg926Lys) c.626G>A (p.Arg209Lys) n.386G>A c.2838-1G>A (n.2838-1G>A) n.7186G>A n.355G>A n.399G>A n.941G>A c.2867G>A (p.Arg956Lys) c.2780G>A (p.Arg927Lys) c.1739G>A (p.Arg580Lys) | |
17 | g.46032169T>A | CA399986831 | KANSL1 | c.2968A>T (p.Arg990Trp) c.2965A>T (p.Arg989Trp) c.2776A>T (p.Arg926Trp) c.625A>T (p.Arg209Trp) n.385A>T c.2838-2A>T (n.2838-2A>T) n.7185A>T n.354A>T n.398A>T n.940A>T c.2866A>T (p.Arg956Trp) c.2779A>T (p.Arg927Trp) c.1738A>T (p.Arg580Trp) | |
17 | g.46032169T>C | CA399986833 | KANSL1 | c.2968A>G (p.Arg990Gly) c.2965A>G (p.Arg989Gly) c.2776A>G (p.Arg926Gly) c.625A>G (p.Arg209Gly) n.385A>G c.2838-2A>G (n.2838-2A>G) n.7185A>G n.354A>G n.398A>G n.940A>G c.2866A>G (p.Arg956Gly) c.2779A>G (p.Arg927Gly) c.1738A>G (p.Arg580Gly) | |
17 | g.46032169T>G | CA500371999 | KANSL1 | c.2968A>C (p.Arg990=) c.2965A>C (p.Arg989=) c.2776A>C (p.Arg926=) c.625A>C (p.Arg209=) n.385A>C c.2838-2A>C (n.2838-2A>C) n.7185A>C n.354A>C n.398A>C n.940A>C c.2866A>C (p.Arg956=) c.2779A>C (p.Arg927=) c.1738A>C (p.Arg580=) | |
17 | g.46032170A>C | CA500372001 | KANSL1 | c.2967T>G (p.Pro989=) c.2964T>G (p.Pro988=) c.2775T>G (p.Pro925=) c.624T>G (p.Pro208=) n.384T>G c.2838-3T>G (n.2838-3T>G) n.7184T>G n.353T>G n.397T>G n.939T>G c.2865T>G (p.Pro955=) c.2778T>G (p.Pro926=) c.1737T>G (p.Pro579=) | |
17 | g.46032170A>G | CA500372000 | KANSL1 | c.2967T>C (p.Pro989=) c.2964T>C (p.Pro988=) c.2775T>C (p.Pro925=) c.624T>C (p.Pro208=) n.384T>C c.2838-3T>C (n.2838-3T>C) n.7184T>C n.353T>C n.397T>C n.939T>C c.2865T>C (p.Pro955=) c.2778T>C (p.Pro926=) c.1737T>C (p.Pro579=) | |
17 | g.46032170A>T | CA500372002 | KANSL1 | c.2967T>A (p.Pro989=) c.2964T>A (p.Pro988=) c.2775T>A (p.Pro925=) c.624T>A (p.Pro208=) n.384T>A c.2838-3T>A (n.2838-3T>A) n.7184T>A n.353T>A n.397T>A n.939T>A c.2865T>A (p.Pro955=) c.2778T>A (p.Pro926=) c.1737T>A (p.Pro579=) | |
17 | g.46032171G>A | CA399986837 | KANSL1 | c.2966C>T (p.Pro989Leu) c.2963C>T (p.Pro988Leu) c.2774C>T (p.Pro925Leu) c.623C>T (p.Pro208Leu) n.383C>T c.2838-4C>T (n.2838-4C>T) n.7183C>T n.352C>T n.396C>T n.938C>T c.2864C>T (p.Pro955Leu) c.2777C>T (p.Pro926Leu) c.1736C>T (p.Pro579Leu) | COSMIC |
17 | g.46032171G>C | CA399986840 | KANSL1 | c.2966C>G (p.Pro989Arg) c.2963C>G (p.Pro988Arg) c.2774C>G (p.Pro925Arg) c.623C>G (p.Pro208Arg) n.383C>G c.2838-4C>G (n.2838-4C>G) n.7183C>G n.352C>G n.396C>G n.938C>G c.2864C>G (p.Pro955Arg) c.2777C>G (p.Pro926Arg) c.1736C>G (p.Pro579Arg) | ClinVar gnomAD v4 |
17 | g.46032171G>T | CA399986842 | KANSL1 | c.2966C>A (p.Pro989His) c.2963C>A (p.Pro988His) c.2774C>A (p.Pro925His) c.623C>A (p.Pro208His) n.383C>A c.2838-4C>A (n.2838-4C>A) n.7183C>A n.352C>A n.396C>A n.938C>A c.2864C>A (p.Pro955His) c.2777C>A (p.Pro926His) c.1736C>A (p.Pro579His) | |
17 | g.46032172G>A | CA399986846 | KANSL1 | c.2965C>T (p.Pro989Ser) c.2962C>T (p.Pro988Ser) c.2773C>T (p.Pro925Ser) c.622C>T (p.Pro208Ser) n.382C>T c.2838-5C>T (n.2838-5C>T) n.7182C>T n.351C>T n.395C>T n.937C>T c.2863C>T (p.Pro955Ser) c.2776C>T (p.Pro926Ser) c.1735C>T (p.Pro579Ser) | |
17 | g.46032172G>C | CA399986848 | KANSL1 | c.2965C>G (p.Pro989Ala) c.2962C>G (p.Pro988Ala) c.2773C>G (p.Pro925Ala) c.622C>G (p.Pro208Ala) n.382C>G c.2838-5C>G (n.2838-5C>G) n.7182C>G n.351C>G n.395C>G n.937C>G c.2863C>G (p.Pro955Ala) c.2776C>G (p.Pro926Ala) c.1735C>G (p.Pro579Ala) | |
17 | g.46032172G= | CA2262111028 | KANSL1 | c.2965C= (p.Pro989=) c.2962C= (p.Pro988=) c.2773C= (p.Pro925=) c.622C= (p.Pro208=) n.382C= c.2838-5C= (n.2838-5C=) n.7182C= n.351C= n.395C= n.937C= c.2863C= (p.Pro955=) c.2776C= (p.Pro926=) c.1735C= (p.Pro579=) | |
17 | g.46032172G>T | CA399986852 | KANSL1 | c.2965C>A (p.Pro989Thr) c.2962C>A (p.Pro988Thr) c.2773C>A (p.Pro925Thr) c.622C>A (p.Pro208Thr) n.382C>A c.2838-5C>A (n.2838-5C>A) n.7182C>A n.351C>A n.395C>A n.937C>A c.2863C>A (p.Pro955Thr) c.2776C>A (p.Pro926Thr) c.1735C>A (p.Pro579Thr) | dbSNP |
17 | g.46032173G>A | CA500372004 | KANSL1 | c.2964C>T (p.Ser988=) c.2961C>T (p.Ser987=) c.2772C>T (p.Ser924=) c.621C>T (p.Ser207=) n.381C>T c.2838-6C>T (n.2838-6C>T) n.7181C>T n.350C>T n.394C>T n.936C>T c.2862C>T (p.Ser954=) c.2775C>T (p.Ser925=) c.1734C>T (p.Ser578=) | |
17 | g.46032173G>C | CA500372003 | KANSL1 | c.2964C>G (p.Ser988=) c.2961C>G (p.Ser987=) c.2772C>G (p.Ser924=) c.621C>G (p.Ser207=) n.381C>G c.2838-6C>G (n.2838-6C>G) n.7181C>G n.350C>G n.394C>G n.936C>G c.2862C>G (p.Ser954=) c.2775C>G (p.Ser925=) c.1734C>G (p.Ser578=) | |
17 | g.46032173G>T | CA500372005 | KANSL1 | c.2964C>A (p.Ser988=) c.2961C>A (p.Ser987=) c.2772C>A (p.Ser924=) c.621C>A (p.Ser207=) n.381C>A c.2838-6C>A (n.2838-6C>A) n.7181C>A n.350C>A n.394C>A n.936C>A c.2862C>A (p.Ser954=) c.2775C>A (p.Ser925=) c.1734C>A (p.Ser578=) | |
17 | g.46032174G>A | CA399986855 | KANSL1 | c.2963C>T (p.Ser988Phe) c.2960C>T (p.Ser987Phe) c.2771C>T (p.Ser924Phe) c.620C>T (p.Ser207Phe) n.380C>T c.2838-7C>T (n.2838-7C>T) n.7180C>T n.349C>T n.393C>T n.935C>T c.2861C>T (p.Ser954Phe) c.2774C>T (p.Ser925Phe) c.1733C>T (p.Ser578Phe) | |
17 | g.46032174G>C | CA399986857 | KANSL1 | c.2963C>G (p.Ser988Cys) c.2960C>G (p.Ser987Cys) c.2771C>G (p.Ser924Cys) c.620C>G (p.Ser207Cys) n.380C>G c.2838-7C>G (n.2838-7C>G) n.7180C>G n.349C>G n.393C>G n.935C>G c.2861C>G (p.Ser954Cys) c.2774C>G (p.Ser925Cys) c.1733C>G (p.Ser578Cys) | |
17 | g.46032174G>T | CA399986860 | KANSL1 | c.2963C>A (p.Ser988Tyr) c.2960C>A (p.Ser987Tyr) c.2771C>A (p.Ser924Tyr) c.620C>A (p.Ser207Tyr) n.380C>A c.2838-7C>A (n.2838-7C>A) n.7180C>A n.349C>A n.393C>A n.935C>A c.2861C>A (p.Ser954Tyr) c.2774C>A (p.Ser925Tyr) c.1733C>A (p.Ser578Tyr) | ClinVar gnomAD v4 |
17 | g.46032175A>C | CA399986865 | KANSL1 | c.2962T>G (p.Ser988Ala) c.2959T>G (p.Ser987Ala) c.2770T>G (p.Ser924Ala) c.619T>G (p.Ser207Ala) n.379T>G c.2838-8T>G (n.2838-8T>G) n.7179T>G n.348T>G n.392T>G n.934T>G c.2860T>G (p.Ser954Ala) c.2773T>G (p.Ser925Ala) c.1732T>G (p.Ser578Ala) | |
17 | g.46032175A>G | CA399986870 | KANSL1 | c.2962T>C (p.Ser988Pro) c.2959T>C (p.Ser987Pro) c.2770T>C (p.Ser924Pro) c.619T>C (p.Ser207Pro) n.379T>C c.2838-8T>C (n.2838-8T>C) n.7179T>C n.348T>C n.392T>C n.934T>C c.2860T>C (p.Ser954Pro) c.2773T>C (p.Ser925Pro) c.1732T>C (p.Ser578Pro) | |
17 | g.46032175A>T | CA399986867 | KANSL1 | c.2962T>A (p.Ser988Thr) c.2959T>A (p.Ser987Thr) c.2770T>A (p.Ser924Thr) c.619T>A (p.Ser207Thr) n.379T>A c.2838-8T>A (n.2838-8T>A) n.7179T>A n.348T>A n.392T>A n.934T>A c.2860T>A (p.Ser954Thr) c.2773T>A (p.Ser925Thr) c.1732T>A (p.Ser578Thr) | |
17 | g.46032176C>A | CA399986882 | KANSL1 | c.2961G>T (p.Gln987His) c.2958G>T (p.Gln986His) c.2769G>T (p.Gln923His) c.618G>T (p.Gln206His) n.378G>T c.2838-9G>T (n.2838-9G>T) n.7178G>T n.347G>T n.391G>T n.933G>T c.2859G>T (p.Gln953His) c.2772G>T (p.Gln924His) c.1731G>T (p.Gln577His) | |
17 | g.46032176C>G | CA399986886 | KANSL1 | c.2961G>C (p.Gln987His) c.2958G>C (p.Gln986His) c.2769G>C (p.Gln923His) c.618G>C (p.Gln206His) n.378G>C c.2838-9G>C (n.2838-9G>C) n.7178G>C n.347G>C n.391G>C n.933G>C c.2859G>C (p.Gln953His) c.2772G>C (p.Gln924His) c.1731G>C (p.Gln577His) | |
17 | g.46032176C>T | CA500372006 | KANSL1 | c.2961G>A (p.Gln987=) c.2958G>A (p.Gln986=) c.2769G>A (p.Gln923=) c.618G>A (p.Gln206=) n.378G>A c.2838-9G>A (n.2838-9G>A) n.7178G>A n.347G>A n.391G>A n.933G>A c.2859G>A (p.Gln953=) c.2772G>A (p.Gln924=) c.1731G>A (p.Gln577=) | |
17 | g.46032177T>A | CA399986889 | KANSL1 | c.2960A>T (p.Gln987Leu) c.2957A>T (p.Gln986Leu) c.2768A>T (p.Gln923Leu) c.617A>T (p.Gln206Leu) n.377A>T c.2838-10A>T (n.2838-10A>T) n.7177A>T n.346A>T n.390A>T n.932A>T c.2858A>T (p.Gln953Leu) c.2771A>T (p.Gln924Leu) c.1730A>T (p.Gln577Leu) | |
17 | g.46032177T>C | CA399986893 | KANSL1 | c.2960A>G (p.Gln987Arg) c.2957A>G (p.Gln986Arg) c.2768A>G (p.Gln923Arg) c.617A>G (p.Gln206Arg) n.377A>G c.2838-10A>G (n.2838-10A>G) n.7177A>G n.346A>G n.390A>G n.932A>G c.2858A>G (p.Gln953Arg) c.2771A>G (p.Gln924Arg) c.1730A>G (p.Gln577Arg) | dbSNP gnomAD v4 |
17 | g.46032177T>G | CA399986895 | KANSL1 | c.2960A>C (p.Gln987Pro) c.2957A>C (p.Gln986Pro) c.2768A>C (p.Gln923Pro) c.617A>C (p.Gln206Pro) n.377A>C c.2838-10A>C (n.2838-10A>C) n.7177A>C n.346A>C n.390A>C n.932A>C c.2858A>C (p.Gln953Pro) c.2771A>C (p.Gln924Pro) c.1730A>C (p.Gln577Pro) | |
17 | g.46032177T= | CA2262111029 | KANSL1 | c.2960A= (p.Gln987=) c.2957A= (p.Gln986=) c.2768A= (p.Gln923=) c.617A= (p.Gln206=) n.377A= c.2838-10A= (n.2838-10A=) n.7177A= n.346A= n.390A= n.932A= c.2858A= (p.Gln953=) c.2771A= (p.Gln924=) c.1730A= (p.Gln577=) | |
17 | g.46032178G>A | CA399986899 | KANSL1 | c.2959C>T (p.Gln987Ter) c.2956C>T (p.Gln986Ter) c.2767C>T (p.Gln923Ter) c.616C>T (p.Gln206Ter) n.376C>T c.2838-11C>T (n.2838-11C>T) n.7176C>T n.345C>T n.389C>T n.931C>T c.2857C>T (p.Gln953Ter) c.2770C>T (p.Gln924Ter) c.1729C>T (p.Gln577Ter) | |
17 | g.46032178G>C | CA399986902 | KANSL1 | c.2959C>G (p.Gln987Glu) c.2956C>G (p.Gln986Glu) c.2767C>G (p.Gln923Glu) c.616C>G (p.Gln206Glu) n.376C>G c.2838-11C>G (n.2838-11C>G) n.7176C>G n.345C>G n.389C>G n.931C>G c.2857C>G (p.Gln953Glu) c.2770C>G (p.Gln924Glu) c.1729C>G (p.Gln577Glu) | |
17 | g.46032178G>T | CA399986903 | KANSL1 | c.2959C>A (p.Gln987Lys) c.2956C>A (p.Gln986Lys) c.2767C>A (p.Gln923Lys) c.616C>A (p.Gln206Lys) n.376C>A c.2838-11C>A (n.2838-11C>A) n.7176C>A n.345C>A n.389C>A n.931C>A c.2857C>A (p.Gln953Lys) c.2770C>A (p.Gln924Lys) c.1729C>A (p.Gln577Lys) | |
17 | g.46032179A= | CA2262111030 | KANSL1 | c.2958T= (p.Gly986=) c.2955T= (p.Gly985=) c.2766T= (p.Gly922=) c.615T= (p.Gly205=) n.375T= c.2838-12T= (n.2838-12T=) n.7175T= n.344T= n.388T= n.930T= c.2856T= (p.Gly952=) c.2769T= (p.Gly923=) c.1728T= (p.Gly576=) | |
17 | g.46032179A>C | CA8618410 | KANSL1 | c.2958T>G (p.Gly986=) c.2955T>G (p.Gly985=) c.2766T>G (p.Gly922=) c.615T>G (p.Gly205=) n.375T>G c.2838-12T>G (n.2838-12T>G) n.7175T>G n.344T>G n.388T>G n.930T>G c.2856T>G (p.Gly952=) c.2769T>G (p.Gly923=) c.1728T>G (p.Gly576=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.46032179A>G | CA500372007 | KANSL1 | c.2958T>C (p.Gly986=) c.2955T>C (p.Gly985=) c.2766T>C (p.Gly922=) c.615T>C (p.Gly205=) n.375T>C c.2838-12T>C (n.2838-12T>C) n.7175T>C n.344T>C n.388T>C n.930T>C c.2856T>C (p.Gly952=) c.2769T>C (p.Gly923=) c.1728T>C (p.Gly576=) | ClinVar dbSNP |
17 | g.46032179A>T | CA500372008 | KANSL1 | c.2958T>A (p.Gly986=) c.2955T>A (p.Gly985=) c.2766T>A (p.Gly922=) c.615T>A (p.Gly205=) n.375T>A c.2838-12T>A (n.2838-12T>A) n.7175T>A n.344T>A n.388T>A n.930T>A c.2856T>A (p.Gly952=) c.2769T>A (p.Gly923=) c.1728T>A (p.Gly576=) | |
17 | g.46032179_46032181delinsACC | CA2262111031 | KANSL1 | c.2956_2958delinsGGT (p.Gly986=) c.2953_2955delinsGGT (p.Gly985=) c.2764_2766delinsGGT (p.Gly922=) c.613_615delinsGGT (p.Gly205=) n.373_375delinsGGT c.2838-14_2838-12delinsGGT (n.2838-14_2838-12delinsGGT) n.7173_7175delinsGGT n.342_344delinsGGT n.386_388delinsGGT n.928_930delinsGGT c.2854_2856delinsGGT (p.Gly952=) c.2767_2769delinsGGT (p.Gly923=) c.1726_1728delinsGGT (p.Gly576=) | |
17 | g.46032180C>A | CA399986913 | KANSL1 | c.2957G>T (p.Gly986Val) c.2954G>T (p.Gly985Val) c.2765G>T (p.Gly922Val) c.614G>T (p.Gly205Val) n.374G>T c.2838-13G>T (n.2838-13G>T) n.7174G>T n.343G>T n.387G>T n.929G>T c.2855G>T (p.Gly952Val) c.2768G>T (p.Gly923Val) c.1727G>T (p.Gly576Val) | |
17 | g.46032180C= | CA2262111032 | KANSL1 | c.2957G= (p.Gly986=) c.2954G= (p.Gly985=) c.2765G= (p.Gly922=) c.614G= (p.Gly205=) n.374G= c.2838-13G= (n.2838-13G=) n.7174G= n.343G= n.387G= n.929G= c.2855G= (p.Gly952=) c.2768G= (p.Gly923=) c.1727G= (p.Gly576=) | |
17 | g.46032180C>G | CA291125908 | KANSL1 | c.2957G>C (p.Gly986Ala) c.2954G>C (p.Gly985Ala) c.2765G>C (p.Gly922Ala) c.614G>C (p.Gly205Ala) n.374G>C c.2838-13G>C (n.2838-13G>C) n.7174G>C n.343G>C n.387G>C n.929G>C c.2855G>C (p.Gly952Ala) c.2768G>C (p.Gly923Ala) c.1727G>C (p.Gly576Ala) | ClinVar dbSNP gnomAD v4 |
17 | g.46032180C>T | CA399986910 | KANSL1 | c.2957G>A (p.Gly986Asp) c.2954G>A (p.Gly985Asp) c.2765G>A (p.Gly922Asp) c.614G>A (p.Gly205Asp) n.374G>A c.2838-13G>A (n.2838-13G>A) n.7174G>A n.343G>A n.387G>A n.929G>A c.2855G>A (p.Gly952Asp) c.2768G>A (p.Gly923Asp) c.1727G>A (p.Gly576Asp) | |
17 | g.46032180_46032181del | CA915950166 | KANSL1 | c.2956_2957del (p.Gly986SerfsTer4) c.2953_2954del (p.Gly985SerfsTer4) c.2764_2765del (p.Gly922SerfsTer4) c.613_614del (p.Gly205SerfsTer4) n.373_374del c.2838-14_2838-13del (n.2838-14_2838-13del) n.7173_7174del n.342_343del n.386_387del n.928_929del c.2854_2855del (p.Gly952SerfsTer4) c.2767_2768del (p.Gly923SerfsTer4) c.1726_1727del (p.Gly576SerfsTer4) | ClinVar dbSNP |
17 | g.46032181C>A | CA399986915 | KANSL1 | c.2956G>T (p.Gly986Cys) c.2953G>T (p.Gly985Cys) c.2764G>T (p.Gly922Cys) c.613G>T (p.Gly205Cys) n.373G>T c.2838-14G>T (n.2838-14G>T) n.7173G>T n.342G>T n.386G>T n.928G>T c.2854G>T (p.Gly952Cys) c.2767G>T (p.Gly923Cys) c.1726G>T (p.Gly576Cys) | |
17 | g.46032181C>G | CA399986917 | KANSL1 | c.2956G>C (p.Gly986Arg) c.2953G>C (p.Gly985Arg) c.2764G>C (p.Gly922Arg) c.613G>C (p.Gly205Arg) n.373G>C c.2838-14G>C (n.2838-14G>C) n.7173G>C n.342G>C n.386G>C n.928G>C c.2854G>C (p.Gly952Arg) c.2767G>C (p.Gly923Arg) c.1726G>C (p.Gly576Arg) | |
17 | g.46032181C>T | CA399986923 | KANSL1 | c.2956G>A (p.Gly986Ser) c.2953G>A (p.Gly985Ser) c.2764G>A (p.Gly922Ser) c.613G>A (p.Gly205Ser) n.373G>A c.2838-14G>A (n.2838-14G>A) n.7173G>A n.342G>A n.386G>A n.928G>A c.2854G>A (p.Gly952Ser) c.2767G>A (p.Gly923Ser) c.1726G>A (p.Gly576Ser) | ClinVar dbSNP gnomAD v4 |
17 | g.46032182A>C | CA399986927 | KANSL1 | c.2955T>G (p.His985Gln) c.2952T>G (p.His984Gln) c.2763T>G (p.His921Gln) c.612T>G (p.His204Gln) n.372T>G c.2838-15T>G (n.2838-15T>G) n.7172T>G n.341T>G n.385T>G n.927T>G c.2853T>G (p.His951Gln) c.2766T>G (p.His922Gln) c.1725T>G (p.His575Gln) | |
17 | g.46032182A>G | CA500372009 | KANSL1 | c.2955T>C (p.His985=) c.2952T>C (p.His984=) c.2763T>C (p.His921=) c.612T>C (p.His204=) n.372T>C c.2838-15T>C (n.2838-15T>C) n.7172T>C n.341T>C n.385T>C n.927T>C c.2853T>C (p.His951=) c.2766T>C (p.His922=) c.1725T>C (p.His575=) | gnomAD v4 |
17 | g.46032182A>T | CA399986928 | KANSL1 | c.2955T>A (p.His985Gln) c.2952T>A (p.His984Gln) c.2763T>A (p.His921Gln) c.612T>A (p.His204Gln) n.372T>A c.2838-15T>A (n.2838-15T>A) n.7172T>A n.341T>A n.385T>A n.927T>A c.2853T>A (p.His951Gln) c.2766T>A (p.His922Gln) c.1725T>A (p.His575Gln) | |
17 | g.46032183T>A | CA399986936 | KANSL1 | c.2954A>T (p.His985Leu) c.2951A>T (p.His984Leu) c.2762A>T (p.His921Leu) c.611A>T (p.His204Leu) n.371A>T c.2838-16A>T (n.2838-16A>T) n.7171A>T n.340A>T n.384A>T n.926A>T c.2852A>T (p.His951Leu) c.2765A>T (p.His922Leu) c.1724A>T (p.His575Leu) | |
17 | g.46032183T>C | CA8618411 | KANSL1 | c.2954A>G (p.His985Arg) c.2951A>G (p.His984Arg) c.2762A>G (p.His921Arg) c.611A>G (p.His204Arg) n.371A>G c.2838-16A>G (n.2838-16A>G) n.7171A>G n.340A>G n.384A>G n.926A>G c.2852A>G (p.His951Arg) c.2765A>G (p.His922Arg) c.1724A>G (p.His575Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.46032183T>G | CA399986934 | KANSL1 | c.2954A>C (p.His985Pro) c.2951A>C (p.His984Pro) c.2762A>C (p.His921Pro) c.611A>C (p.His204Pro) n.371A>C c.2838-16A>C (n.2838-16A>C) n.7171A>C n.340A>C n.384A>C n.926A>C c.2852A>C (p.His951Pro) c.2765A>C (p.His922Pro) c.1724A>C (p.His575Pro) | |
17 | g.46032183T= | CA2262111033 | KANSL1 | c.2954A= (p.His985=) c.2951A= (p.His984=) c.2762A= (p.His921=) c.611A= (p.His204=) n.371A= c.2838-16A= (n.2838-16A=) n.7171A= n.340A= n.384A= n.926A= c.2852A= (p.His951=) c.2765A= (p.His922=) c.1724A= (p.His575=) | |
17 | g.46032184G>A | CA399986940 | KANSL1 | c.2953C>T (p.His985Tyr) c.2950C>T (p.His984Tyr) c.2761C>T (p.His921Tyr) c.610C>T (p.His204Tyr) n.370C>T c.2838-17C>T (n.2838-17C>T) n.7170C>T n.339C>T n.383C>T n.925C>T c.2851C>T (p.His951Tyr) c.2764C>T (p.His922Tyr) c.1723C>T (p.His575Tyr) | gnomAD v4 |
17 | g.46032184G>C | CA399986941 | KANSL1 | c.2953C>G (p.His985Asp) c.2950C>G (p.His984Asp) c.2761C>G (p.His921Asp) c.610C>G (p.His204Asp) n.370C>G c.2838-17C>G (n.2838-17C>G) n.7170C>G n.339C>G n.383C>G n.925C>G c.2851C>G (p.His951Asp) c.2764C>G (p.His922Asp) c.1723C>G (p.His575Asp) | |
17 | g.46032184G>T | CA399986942 | KANSL1 | c.2953C>A (p.His985Asn) c.2950C>A (p.His984Asn) c.2761C>A (p.His921Asn) c.610C>A (p.His204Asn) n.370C>A c.2838-17C>A (n.2838-17C>A) n.7170C>A n.339C>A n.383C>A n.925C>A c.2851C>A (p.His951Asn) c.2764C>A (p.His922Asn) c.1723C>A (p.His575Asn) | gnomAD v4 |
17 | g.46032185G>A | CA500372011 | KANSL1 | c.2952C>T (p.Ser984=) c.2949C>T (p.Ser983=) c.2760C>T (p.Ser920=) c.609C>T (p.Ser203=) n.369C>T c.2838-18C>T (n.2838-18C>T) n.7169C>T n.338C>T n.382C>T n.924C>T c.2850C>T (p.Ser950=) c.2763C>T (p.Ser921=) c.1722C>T (p.Ser574=) | COSMIC |
17 | g.46032185G>C | CA8618412 | KANSL1 | c.2952C>G (p.Ser984=) c.2949C>G (p.Ser983=) c.2760C>G (p.Ser920=) c.609C>G (p.Ser203=) n.369C>G c.2838-18C>G (n.2838-18C>G) n.7169C>G n.338C>G n.382C>G n.924C>G c.2850C>G (p.Ser950=) c.2763C>G (p.Ser921=) c.1722C>G (p.Ser574=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.46032185G= | CA2262111034 | KANSL1 | c.2952C= (p.Ser984=) c.2949C= (p.Ser983=) c.2760C= (p.Ser920=) c.609C= (p.Ser203=) n.369C= c.2838-18C= (n.2838-18C=) n.7169C= n.338C= n.382C= n.924C= c.2850C= (p.Ser950=) c.2763C= (p.Ser921=) c.1722C= (p.Ser574=) | |
17 | g.46032185G>T | CA500372010 | KANSL1 | c.2952C>A (p.Ser984=) c.2949C>A (p.Ser983=) c.2760C>A (p.Ser920=) c.609C>A (p.Ser203=) n.369C>A c.2838-18C>A (n.2838-18C>A) n.7169C>A n.338C>A n.382C>A n.924C>A c.2850C>A (p.Ser950=) c.2763C>A (p.Ser921=) c.1722C>A (p.Ser574=) | |
17 | g.46032186G>A | CA399986944 | KANSL1 | c.2951C>T (p.Ser984Phe) c.2948C>T (p.Ser983Phe) c.2759C>T (p.Ser920Phe) n.899C>T c.608C>T (p.Ser203Phe) n.368C>T c.2838-19C>T (n.2838-19C>T) n.7168C>T n.337C>T n.381C>T n.923C>T c.2849C>T (p.Ser950Phe) c.2762C>T (p.Ser921Phe) c.1721C>T (p.Ser574Phe) | COSMIC |
17 | g.46032186G>C | CA399986948 | KANSL1 | c.2951C>G (p.Ser984Cys) c.2948C>G (p.Ser983Cys) c.2759C>G (p.Ser920Cys) n.899C>G c.608C>G (p.Ser203Cys) n.368C>G c.2838-19C>G (n.2838-19C>G) n.7168C>G n.337C>G n.381C>G n.923C>G c.2849C>G (p.Ser950Cys) c.2762C>G (p.Ser921Cys) c.1721C>G (p.Ser574Cys) | |
17 | g.46032186G= | CA2262111035 | KANSL1 | c.2951C= (p.Ser984=) c.2948C= (p.Ser983=) c.2759C= (p.Ser920=) n.899C= c.608C= (p.Ser203=) n.368C= c.2838-19C= (n.2838-19C=) n.7168C= n.337C= n.381C= n.923C= c.2849C= (p.Ser950=) c.2762C= (p.Ser921=) c.1721C= (p.Ser574=) | |
17 | g.46032186G>T | CA315130 | KANSL1 | c.2951C>A (p.Ser984Tyr) c.2948C>A (p.Ser983Tyr) c.2759C>A (p.Ser920Tyr) n.899C>A c.608C>A (p.Ser203Tyr) n.368C>A c.2838-19C>A (n.2838-19C>A) n.7168C>A n.337C>A n.381C>A n.923C>A c.2849C>A (p.Ser950Tyr) c.2762C>A (p.Ser921Tyr) c.1721C>A (p.Ser574Tyr) | ClinVar dbSNP |
17 | g.46032187A>C | CA399986959 | KANSL1 | c.2950T>G (p.Ser984Ala) c.2947T>G (p.Ser983Ala) c.2758T>G (p.Ser920Ala) n.898T>G c.607T>G (p.Ser203Ala) n.367T>G c.2838-20T>G (n.2838-20T>G) n.7167T>G n.336T>G n.380T>G n.922T>G c.2848T>G (p.Ser950Ala) c.2761T>G (p.Ser921Ala) c.1720T>G (p.Ser574Ala) | |
17 | g.46032187A>G | CA399986962 | KANSL1 | c.2950T>C (p.Ser984Pro) c.2947T>C (p.Ser983Pro) c.2758T>C (p.Ser920Pro) n.898T>C c.607T>C (p.Ser203Pro) n.367T>C c.2838-20T>C (n.2838-20T>C) n.7167T>C n.336T>C n.380T>C n.922T>C c.2848T>C (p.Ser950Pro) c.2761T>C (p.Ser921Pro) c.1720T>C (p.Ser574Pro) | |
17 | g.46032187A>T | CA399986965 | KANSL1 | c.2950T>A (p.Ser984Thr) c.2947T>A (p.Ser983Thr) c.2758T>A (p.Ser920Thr) n.898T>A c.607T>A (p.Ser203Thr) n.367T>A c.2838-20T>A (n.2838-20T>A) n.7167T>A n.336T>A n.380T>A n.922T>A c.2848T>A (p.Ser950Thr) c.2761T>A (p.Ser921Thr) c.1720T>A (p.Ser574Thr) | |
17 | g.46032188G>A | CA291709 | KANSL1 | c.2949C>T (p.Tyr983=) c.2946C>T (p.Tyr982=) c.2757C>T (p.Tyr919=) n.897C>T c.606C>T (p.Tyr202=) n.366C>T c.2838-21C>T (n.2838-21C>T) n.7166C>T n.335C>T n.379C>T n.921C>T c.2847C>T (p.Tyr949=) c.2760C>T (p.Tyr920=) c.1719C>T (p.Tyr573=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.46032188G>C | CA399986972 | KANSL1 | c.2949C>G (p.Tyr983Ter) c.2946C>G (p.Tyr982Ter) c.2757C>G (p.Tyr919Ter) n.897C>G c.606C>G (p.Tyr202Ter) n.366C>G c.2838-21C>G (n.2838-21C>G) n.7166C>G n.335C>G n.379C>G n.921C>G c.2847C>G (p.Tyr949Ter) c.2760C>G (p.Tyr920Ter) c.1719C>G (p.Tyr573Ter) | |
17 | g.46032188G= | CA2262111036 | KANSL1 | c.2949C= (p.Tyr983=) c.2946C= (p.Tyr982=) c.2757C= (p.Tyr919=) n.897C= c.606C= (p.Tyr202=) n.366C= c.2838-21C= (n.2838-21C=) n.7166C= n.335C= n.379C= n.921C= c.2847C= (p.Tyr949=) c.2760C= (p.Tyr920=) c.1719C= (p.Tyr573=) | |
17 | g.46032188G>T | CA399986975 | KANSL1 | c.2949C>A (p.Tyr983Ter) c.2946C>A (p.Tyr982Ter) c.2757C>A (p.Tyr919Ter) n.897C>A c.606C>A (p.Tyr202Ter) n.366C>A c.2838-21C>A (n.2838-21C>A) n.7166C>A n.335C>A n.379C>A n.921C>A c.2847C>A (p.Tyr949Ter) c.2760C>A (p.Tyr920Ter) c.1719C>A (p.Tyr573Ter) | |
17 | g.46032189T>A | CA399986979 | KANSL1 | c.2948A>T (p.Tyr983Phe) c.2945A>T (p.Tyr982Phe) c.2756A>T (p.Tyr919Phe) n.896A>T c.605A>T (p.Tyr202Phe) n.365A>T c.2838-22A>T (n.2838-22A>T) n.7165A>T n.334A>T n.378A>T n.920A>T c.2846A>T (p.Tyr949Phe) c.2759A>T (p.Tyr920Phe) c.1718A>T (p.Tyr573Phe) | |
17 | g.46032189T>C | CA399986982 | KANSL1 | c.2948A>G (p.Tyr983Cys) c.2945A>G (p.Tyr982Cys) c.2756A>G (p.Tyr919Cys) n.896A>G c.605A>G (p.Tyr202Cys) n.365A>G c.2838-22A>G (n.2838-22A>G) n.7165A>G n.334A>G n.378A>G n.920A>G c.2846A>G (p.Tyr949Cys) c.2759A>G (p.Tyr920Cys) c.1718A>G (p.Tyr573Cys) | |
17 | g.46032189T>G | CA399986980 | KANSL1 | c.2948A>C (p.Tyr983Ser) c.2945A>C (p.Tyr982Ser) c.2756A>C (p.Tyr919Ser) n.896A>C c.605A>C (p.Tyr202Ser) n.365A>C c.2838-22A>C (n.2838-22A>C) n.7165A>C n.334A>C n.378A>C n.920A>C c.2846A>C (p.Tyr949Ser) c.2759A>C (p.Tyr920Ser) c.1718A>C (p.Tyr573Ser) | |
17 | g.46032190A>C | CA399986985 | KANSL1 | c.2947T>G (p.Tyr983Asp) c.2944T>G (p.Tyr982Asp) c.2755T>G (p.Tyr919Asp) n.895T>G c.604T>G (p.Tyr202Asp) n.364T>G c.2838-23T>G (n.2838-23T>G) n.7164T>G n.333T>G n.377T>G n.919T>G c.2845T>G (p.Tyr949Asp) c.2758T>G (p.Tyr920Asp) c.1717T>G (p.Tyr573Asp) | |
17 | g.46032190A>G | CA399986988 | KANSL1 | c.2947T>C (p.Tyr983His) c.2944T>C (p.Tyr982His) c.2755T>C (p.Tyr919His) n.895T>C c.604T>C (p.Tyr202His) n.364T>C c.2838-23T>C (n.2838-23T>C) n.7164T>C n.333T>C n.377T>C n.919T>C c.2845T>C (p.Tyr949His) c.2758T>C (p.Tyr920His) c.1717T>C (p.Tyr573His) | |
17 | g.46032190A>T | CA399986990 | KANSL1 | c.2947T>A (p.Tyr983Asn) c.2944T>A (p.Tyr982Asn) c.2755T>A (p.Tyr919Asn) n.895T>A c.604T>A (p.Tyr202Asn) n.364T>A c.2838-23T>A (n.2838-23T>A) n.7164T>A n.333T>A n.377T>A n.919T>A c.2845T>A (p.Tyr949Asn) c.2758T>A (p.Tyr920Asn) c.1717T>A (p.Tyr573Asn) | gnomAD v4 |
17 | g.46032191T>A | CA399986992 | KANSL1 | c.2946A>T (p.Glu982Asp) c.2943A>T (p.Glu981Asp) c.2754A>T (p.Glu918Asp) n.894A>T c.603A>T (p.Glu201Asp) n.363A>T c.2838-24A>T (n.2838-24A>T) n.7163A>T n.332A>T n.376A>T n.918A>T c.2844A>T (p.Glu948Asp) c.2757A>T (p.Glu919Asp) c.1716A>T (p.Glu572Asp) | |
17 | g.46032191T>C | CA291125919 | KANSL1 | c.2946A>G (p.Glu982=) c.2943A>G (p.Glu981=) c.2754A>G (p.Glu918=) n.894A>G c.603A>G (p.Glu201=) n.363A>G c.2838-24A>G (n.2838-24A>G) n.7163A>G n.332A>G n.376A>G n.918A>G c.2844A>G (p.Glu948=) c.2757A>G (p.Glu919=) c.1716A>G (p.Glu572=) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.46032191T>G | CA399986995 | KANSL1 | c.2946A>C (p.Glu982Asp) c.2943A>C (p.Glu981Asp) c.2754A>C (p.Glu918Asp) n.894A>C c.603A>C (p.Glu201Asp) n.363A>C c.2838-24A>C (n.2838-24A>C) n.7163A>C n.332A>C n.376A>C n.918A>C c.2844A>C (p.Glu948Asp) c.2757A>C (p.Glu919Asp) c.1716A>C (p.Glu572Asp) | |
17 | g.46032191T= | CA2262111037 | KANSL1 | c.2946A= (p.Glu982=) c.2943A= (p.Glu981=) c.2754A= (p.Glu918=) n.894A= c.603A= (p.Glu201=) n.363A= c.2838-24A= (n.2838-24A=) n.7163A= n.332A= n.376A= n.918A= c.2844A= (p.Glu948=) c.2757A= (p.Glu919=) c.1716A= (p.Glu572=) | |
17 | g.46032192T>A | CA399987003 | KANSL1 | c.2945A>T (p.Glu982Val) c.2942A>T (p.Glu981Val) c.2753A>T (p.Glu918Val) n.893A>T c.602A>T (p.Glu201Val) n.362A>T c.2838-25A>T (n.2838-25A>T) n.7162A>T n.331A>T n.375A>T n.917A>T c.2843A>T (p.Glu948Val) c.2756A>T (p.Glu919Val) c.1715A>T (p.Glu572Val) | |
17 | g.46032192T>C | CA399987000 | KANSL1 | c.2945A>G (p.Glu982Gly) c.2942A>G (p.Glu981Gly) c.2753A>G (p.Glu918Gly) n.893A>G c.602A>G (p.Glu201Gly) n.362A>G c.2838-25A>G (n.2838-25A>G) n.7162A>G n.331A>G n.375A>G n.917A>G c.2843A>G (p.Glu948Gly) c.2756A>G (p.Glu919Gly) c.1715A>G (p.Glu572Gly) | |
17 | g.46032192T>G | CA399986998 | KANSL1 | c.2945A>C (p.Glu982Ala) c.2942A>C (p.Glu981Ala) c.2753A>C (p.Glu918Ala) n.893A>C c.602A>C (p.Glu201Ala) n.362A>C c.2838-25A>C (n.2838-25A>C) n.7162A>C n.331A>C n.375A>C n.917A>C c.2843A>C (p.Glu948Ala) c.2756A>C (p.Glu919Ala) c.1715A>C (p.Glu572Ala) | |
17 | g.46032193C>A | CA399987007 | KANSL1 | c.2944G>T (p.Glu982Ter) c.2941G>T (p.Glu981Ter) c.2752G>T (p.Glu918Ter) n.892G>T c.601G>T (p.Glu201Ter) n.361G>T c.2838-26G>T (n.2838-26G>T) n.7161G>T n.330G>T n.374G>T n.916G>T c.2842G>T (p.Glu948Ter) c.2755G>T (p.Glu919Ter) c.1714G>T (p.Glu572Ter) | |
17 | g.46032193C>G | CA399987012 | KANSL1 | c.2944G>C (p.Glu982Gln) c.2941G>C (p.Glu981Gln) c.2752G>C (p.Glu918Gln) n.892G>C c.601G>C (p.Glu201Gln) n.361G>C c.2838-26G>C (n.2838-26G>C) n.7161G>C n.330G>C n.374G>C n.916G>C c.2842G>C (p.Glu948Gln) c.2755G>C (p.Glu919Gln) c.1714G>C (p.Glu572Gln) | |
17 | g.46032193C>T | CA399987013 | KANSL1 | c.2944G>A (p.Glu982Lys) c.2941G>A (p.Glu981Lys) c.2752G>A (p.Glu918Lys) n.892G>A c.601G>A (p.Glu201Lys) n.361G>A c.2838-26G>A (n.2838-26G>A) n.7161G>A n.330G>A n.374G>A n.916G>A c.2842G>A (p.Glu948Lys) c.2755G>A (p.Glu919Lys) c.1714G>A (p.Glu572Lys) | |
17 | g.46032194T>A | CA500372014 | KANSL1 | c.2943A>T (p.Ser981=) c.2940A>T (p.Ser980=) c.2751A>T (p.Ser917=) n.891A>T c.600A>T (p.Ser200=) n.360A>T c.2838-27A>T (n.2838-27A>T) n.7160A>T n.329A>T n.373A>T n.915A>T c.2841A>T (p.Ser947=) c.2754A>T (p.Ser918=) c.1713A>T (p.Ser571=) | |
17 | g.46032194T>C | CA500372015 | KANSL1 | c.2943A>G (p.Ser981=) c.2940A>G (p.Ser980=) c.2751A>G (p.Ser917=) n.891A>G c.600A>G (p.Ser200=) n.360A>G c.2838-27A>G (n.2838-27A>G) n.7160A>G n.329A>G n.373A>G n.915A>G c.2841A>G (p.Ser947=) c.2754A>G (p.Ser918=) c.1713A>G (p.Ser571=) | |
17 | g.46032194T>G | CA500372013 | KANSL1 | c.2943A>C (p.Ser981=) c.2940A>C (p.Ser980=) c.2751A>C (p.Ser917=) n.891A>C c.600A>C (p.Ser200=) n.360A>C c.2838-27A>C (n.2838-27A>C) n.7160A>C n.329A>C n.373A>C n.915A>C c.2841A>C (p.Ser947=) c.2754A>C (p.Ser918=) c.1713A>C (p.Ser571=) | |
17 | g.46032195G>A | CA399987016 | KANSL1 | c.2942C>T (p.Ser981Leu) c.2939C>T (p.Ser980Leu) c.2750C>T (p.Ser917Leu) n.890C>T c.599C>T (p.Ser200Leu) n.359C>T c.2838-28C>T (n.2838-28C>T) n.7159C>T n.328C>T n.372C>T n.914C>T c.2840C>T (p.Ser947Leu) c.2753C>T (p.Ser918Leu) c.1712C>T (p.Ser571Leu) | |
17 | g.46032195G>C | CA399987019 | KANSL1 | c.2942C>G (p.Ser981Ter) c.2939C>G (p.Ser980Ter) c.2750C>G (p.Ser917Ter) n.890C>G c.599C>G (p.Ser200Ter) n.359C>G c.2838-28C>G (n.2838-28C>G) n.7159C>G n.328C>G n.372C>G n.914C>G c.2840C>G (p.Ser947Ter) c.2753C>G (p.Ser918Ter) c.1712C>G (p.Ser571Ter) | |
17 | g.46032195G>T | CA399987027 | KANSL1 | c.2942C>A (p.Ser981Ter) c.2939C>A (p.Ser980Ter) c.2750C>A (p.Ser917Ter) n.890C>A c.599C>A (p.Ser200Ter) n.359C>A c.2838-28C>A (n.2838-28C>A) n.7159C>A n.328C>A n.372C>A n.914C>A c.2840C>A (p.Ser947Ter) c.2753C>A (p.Ser918Ter) c.1712C>A (p.Ser571Ter) | |
17 | g.46032196A= | CA2262111038 | KANSL1 | c.2941T= (p.Ser981=) c.2938T= (p.Ser980=) c.2749T= (p.Ser917=) n.889T= c.598T= (p.Ser200=) n.358T= c.2838-29T= (n.2838-29T=) n.7158T= n.327T= n.371T= n.913T= c.2839T= (p.Ser947=) c.2752T= (p.Ser918=) c.1711T= (p.Ser571=) | |
17 | g.46032196A>C | CA399987031 | KANSL1 | c.2941T>G (p.Ser981Ala) c.2938T>G (p.Ser980Ala) c.2749T>G (p.Ser917Ala) n.889T>G c.598T>G (p.Ser200Ala) n.358T>G c.2838-29T>G (n.2838-29T>G) n.7158T>G n.327T>G n.371T>G n.913T>G c.2839T>G (p.Ser947Ala) c.2752T>G (p.Ser918Ala) c.1711T>G (p.Ser571Ala) | |
17 | g.46032196A>G | CA399987035 | KANSL1 | c.2941T>C (p.Ser981Pro) c.2938T>C (p.Ser980Pro) c.2749T>C (p.Ser917Pro) n.889T>C c.598T>C (p.Ser200Pro) n.358T>C c.2838-29T>C (n.2838-29T>C) n.7158T>C n.327T>C n.371T>C n.913T>C c.2839T>C (p.Ser947Pro) c.2752T>C (p.Ser918Pro) c.1711T>C (p.Ser571Pro) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.46032196A>T | CA399987034 | KANSL1 | c.2941T>A (p.Ser981Thr) c.2938T>A (p.Ser980Thr) c.2749T>A (p.Ser917Thr) n.889T>A c.598T>A (p.Ser200Thr) n.358T>A c.2838-29T>A (n.2838-29T>A) n.7158T>A n.327T>A n.371T>A n.913T>A c.2839T>A (p.Ser947Thr) c.2752T>A (p.Ser918Thr) c.1711T>A (p.Ser571Thr) | |
17 | g.46032197_46032198del | CA2695226190 | KANSL1 | c.2940_2941del (p.Leu980PhefsTer10) c.2937_2938del (p.Leu979PhefsTer10) c.2748_2749del (p.Leu916PhefsTer10) n.888_889del c.597_598del (p.Leu199PhefsTer10) n.357_358del c.2838-30_2838-29del (n.2838-30_2838-29del) n.7157_7158del n.326_327del n.370_371del n.912_913del c.2838_2839del (p.Leu946PhefsTer10) c.2751_2752del (p.Leu917PhefsTer10) c.1710_1711del (p.Leu570PhefsTer10) | |
17 | g.46032197C>A | CA399987036 | KANSL1 | c.2940G>T (p.Leu980Phe) c.2937G>T (p.Leu979Phe) c.2748G>T (p.Leu916Phe) n.888G>T c.597G>T (p.Leu199Phe) n.357G>T c.2838-30G>T (n.2838-30G>T) n.7157G>T n.326G>T n.370G>T n.912G>T c.2838G>T (p.Leu946Phe) c.2751G>T (p.Leu917Phe) c.1710G>T (p.Leu570Phe) | |
17 | g.46032197C= | CA2262111040 | KANSL1 | c.2940G= (p.Leu980=) c.2937G= (p.Leu979=) c.2748G= (p.Leu916=) n.888G= c.597G= (p.Leu199=) n.357G= c.2838-30G= (n.2838-30G=) n.7157G= n.326G= n.370G= n.912G= c.2838G= (p.Leu946=) c.2751G= (p.Leu917=) c.1710G= (p.Leu570=) | |
17 | g.46032197C>G | CA399987037 | KANSL1 | c.2940G>C (p.Leu980Phe) c.2937G>C (p.Leu979Phe) c.2748G>C (p.Leu916Phe) n.888G>C c.597G>C (p.Leu199Phe) n.357G>C c.2838-30G>C (n.2838-30G>C) n.7157G>C n.326G>C n.370G>C n.912G>C c.2838G>C (p.Leu946Phe) c.2751G>C (p.Leu917Phe) c.1710G>C (p.Leu570Phe) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.46032197C>T | CA500372016 | KANSL1 | c.2940G>A (p.Leu980=) c.2937G>A (p.Leu979=) c.2748G>A (p.Leu916=) n.888G>A c.597G>A (p.Leu199=) n.357G>A c.2838-30G>A (n.2838-30G>A) n.7157G>A n.326G>A n.370G>A n.912G>A c.2838G>A (p.Leu946=) c.2751G>A (p.Leu917=) c.1710G>A (p.Leu570=) | gnomAD v4 |
17 | g.46032197_46032199delinsCAA | CA2262111039 | KANSL1 | c.2938_2940delinsTTG (p.Leu980=) c.2935_2937delinsTTG (p.Leu979=) c.2746_2748delinsTTG (p.Leu916=) n.886_888delinsTTG c.595_597delinsTTG (p.Leu199=) n.355_357delinsTTG c.2838-32_2838-30delinsTTG (n.2838-32_2838-30delinsTTG) n.7155_7157delinsTTG n.324_326delinsTTG n.368_370delinsTTG n.910_912delinsTTG c.2836_2838delinsTTG (p.Leu946=) c.2749_2751delinsTTG (p.Leu917=) c.1708_1710delinsTTG (p.Leu570=) | |
17 | g.46032198A= | CA2262111041 | KANSL1 | c.2939T= (p.Leu980=) c.2936T= (p.Leu979=) c.2747T= (p.Leu916=) n.887T= c.596T= (p.Leu199=) n.356T= c.2838-31T= (n.2838-31T=) n.7156T= n.325T= n.369T= n.911T= c.2837T= (p.Leu946=) c.2750T= (p.Leu917=) c.1709T= (p.Leu570=) | |
17 | g.46032198A>C | CA399987039 | KANSL1 | c.2939T>G (p.Leu980Trp) c.2936T>G (p.Leu979Trp) c.2747T>G (p.Leu916Trp) n.887T>G c.596T>G (p.Leu199Trp) n.356T>G c.2838-31T>G (n.2838-31T>G) n.7156T>G n.325T>G n.369T>G n.911T>G c.2837T>G (p.Leu946Trp) c.2750T>G (p.Leu917Trp) c.1709T>G (p.Leu570Trp) | |
17 | g.46032198A>G | CA399987042 | KANSL1 | c.2939T>C (p.Leu980Ser) c.2936T>C (p.Leu979Ser) c.2747T>C (p.Leu916Ser) n.887T>C c.596T>C (p.Leu199Ser) n.356T>C c.2838-31T>C (n.2838-31T>C) n.7156T>C n.325T>C n.369T>C n.911T>C c.2837T>C (p.Leu946Ser) c.2750T>C (p.Leu917Ser) c.1709T>C (p.Leu570Ser) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.46032198A>T | CA399987046 | KANSL1 | c.2939T>A (p.Leu980Ter) c.2936T>A (p.Leu979Ter) c.2747T>A (p.Leu916Ter) n.887T>A c.596T>A (p.Leu199Ter) n.356T>A c.2838-31T>A (n.2838-31T>A) n.7156T>A n.325T>A n.369T>A n.911T>A c.2837T>A (p.Leu946Ter) c.2750T>A (p.Leu917Ter) c.1709T>A (p.Leu570Ter) | |
17 | g.46032199_46032200del | CA913191107 | KANSL1 | c.2938_2939del (p.Leu980ValfsTer10) c.2935_2936del (p.Leu979ValfsTer10) c.2746_2747del (p.Leu916ValfsTer10) n.886_887del c.595_596del (p.Leu199ValfsTer10) n.355_356del c.2838-32_2838-31del (n.2838-32_2838-31del) n.7155_7156del n.324_325del n.368_369del n.910_911del c.2836_2837del (p.Leu946ValfsTer10) c.2749_2750del (p.Leu917ValfsTer10) c.1708_1709del (p.Leu570ValfsTer10) | ClinVar |
17 | g.46032199A>C | CA399987049 | KANSL1 | c.2938T>G (p.Leu980Val) c.2935T>G (p.Leu979Val) c.2746T>G (p.Leu916Val) n.886T>G c.595T>G (p.Leu199Val) n.355T>G c.2838-32T>G (n.2838-32T>G) n.7155T>G n.324T>G n.368T>G n.910T>G c.2836T>G (p.Leu946Val) c.2749T>G (p.Leu917Val) c.1708T>G (p.Leu570Val) | |
17 | g.46032199A>G | CA500372017 | KANSL1 | c.2938T>C (p.Leu980=) c.2935T>C (p.Leu979=) c.2746T>C (p.Leu916=) n.886T>C c.595T>C (p.Leu199=) n.355T>C c.2838-32T>C (n.2838-32T>C) n.7155T>C n.324T>C n.368T>C n.910T>C c.2836T>C (p.Leu946=) c.2749T>C (p.Leu917=) c.1708T>C (p.Leu570=) | |
17 | g.46032199A>T | CA399987051 | KANSL1 | c.2938T>A (p.Leu980Met) c.2935T>A (p.Leu979Met) c.2746T>A (p.Leu916Met) n.886T>A c.595T>A (p.Leu199Met) n.355T>A c.2838-32T>A (n.2838-32T>A) n.7155T>A n.324T>A n.368T>A n.910T>A c.2836T>A (p.Leu946Met) c.2749T>A (p.Leu917Met) c.1708T>A (p.Leu570Met) | |
17 | g.46032200A>C | CA500372019 | KANSL1 | c.2937T>G (p.Ser979=) c.2934T>G (p.Ser978=) c.2745T>G (p.Ser915=) n.885T>G c.594T>G (p.Ser198=) n.354T>G c.2838-33T>G (n.2838-33T>G) n.7154T>G n.323T>G n.367T>G n.909T>G c.2835T>G (p.Ser945=) c.2748T>G (p.Ser916=) c.1707T>G (p.Ser569=) | |
17 | g.46032200A>G | CA500372020 | KANSL1 | c.2937T>C (p.Ser979=) c.2934T>C (p.Ser978=) c.2745T>C (p.Ser915=) n.885T>C c.594T>C (p.Ser198=) n.354T>C c.2838-33T>C (n.2838-33T>C) n.7154T>C n.323T>C n.367T>C n.909T>C c.2835T>C (p.Ser945=) c.2748T>C (p.Ser916=) c.1707T>C (p.Ser569=) | gnomAD v4 |
17 | g.46032200A>T | CA500372018 | KANSL1 | c.2937T>A (p.Ser979=) c.2934T>A (p.Ser978=) c.2745T>A (p.Ser915=) n.885T>A c.594T>A (p.Ser198=) n.354T>A c.2838-33T>A (n.2838-33T>A) n.7154T>A n.323T>A n.367T>A n.909T>A c.2835T>A (p.Ser945=) c.2748T>A (p.Ser916=) c.1707T>A (p.Ser569=) | |
17 | g.46032201G>A | CA399987054 | KANSL1 | c.2936C>T (p.Ser979Phe) c.2933C>T (p.Ser978Phe) c.2744C>T (p.Ser915Phe) n.884C>T c.593C>T (p.Ser198Phe) n.353C>T c.2838-34C>T (n.2838-34C>T) n.7153C>T n.322C>T n.366C>T n.908C>T c.2834C>T (p.Ser945Phe) c.2747C>T (p.Ser916Phe) c.1706C>T (p.Ser569Phe) | |
17 | g.46032201G>C | CA399987056 | KANSL1 | c.2936C>G (p.Ser979Cys) c.2933C>G (p.Ser978Cys) c.2744C>G (p.Ser915Cys) n.884C>G c.593C>G (p.Ser198Cys) n.353C>G c.2838-34C>G (n.2838-34C>G) n.7153C>G n.322C>G n.366C>G n.908C>G c.2834C>G (p.Ser945Cys) c.2747C>G (p.Ser916Cys) c.1706C>G (p.Ser569Cys) | |
17 | g.46032201G>T | CA399987059 | KANSL1 | c.2936C>A (p.Ser979Tyr) c.2933C>A (p.Ser978Tyr) c.2744C>A (p.Ser915Tyr) n.884C>A c.593C>A (p.Ser198Tyr) n.353C>A c.2838-34C>A (n.2838-34C>A) n.7153C>A n.322C>A n.366C>A n.908C>A c.2834C>A (p.Ser945Tyr) c.2747C>A (p.Ser916Tyr) c.1706C>A (p.Ser569Tyr) | |
17 | g.46032202A>C | CA399987062 | KANSL1 | c.2935T>G (p.Ser979Ala) c.2932T>G (p.Ser978Ala) c.2743T>G (p.Ser915Ala) n.883T>G c.592T>G (p.Ser198Ala) n.352T>G c.2838-35T>G (n.2838-35T>G) n.7152T>G n.321T>G n.365T>G n.907T>G c.2833T>G (p.Ser945Ala) c.2746T>G (p.Ser916Ala) c.1705T>G (p.Ser569Ala) | |
17 | g.46032202A>G | CA399987065 | KANSL1 | c.2935T>C (p.Ser979Pro) c.2932T>C (p.Ser978Pro) c.2743T>C (p.Ser915Pro) n.883T>C c.592T>C (p.Ser198Pro) n.352T>C c.2838-35T>C (n.2838-35T>C) n.7152T>C n.321T>C n.365T>C n.907T>C c.2833T>C (p.Ser945Pro) c.2746T>C (p.Ser916Pro) c.1705T>C (p.Ser569Pro) | |
17 | g.46032202A>T | CA399987063 | KANSL1 | c.2935T>A (p.Ser979Thr) c.2932T>A (p.Ser978Thr) c.2743T>A (p.Ser915Thr) n.883T>A c.592T>A (p.Ser198Thr) n.352T>A c.2838-35T>A (n.2838-35T>A) n.7152T>A n.321T>A n.365T>A n.907T>A c.2833T>A (p.Ser945Thr) c.2746T>A (p.Ser916Thr) c.1705T>A (p.Ser569Thr) | |
17 | g.46032203G>A | CA500372021 | KANSL1 | c.2934C>T (p.His978=) c.2931C>T (p.His977=) c.2742C>T (p.His914=) n.882C>T c.591C>T (p.His197=) n.351C>T c.2838-36C>T (n.2838-36C>T) n.7151C>T n.320C>T n.364C>T n.906C>T c.2832C>T (p.His944=) c.2745C>T (p.His915=) c.1704C>T (p.His568=) | gnomAD v4 |
17 | g.46032203G>C | CA8618413 | KANSL1 | c.2934C>G (p.His978Gln) c.2931C>G (p.His977Gln) c.2742C>G (p.His914Gln) n.882C>G c.591C>G (p.His197Gln) n.351C>G c.2838-36C>G (n.2838-36C>G) n.7151C>G n.320C>G n.364C>G n.906C>G c.2832C>G (p.His944Gln) c.2745C>G (p.His915Gln) c.1704C>G (p.His568Gln) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.46032203G= | CA2262111042 | KANSL1 | c.2934C= (p.His978=) c.2931C= (p.His977=) c.2742C= (p.His914=) n.882C= c.591C= (p.His197=) n.351C= c.2838-36C= (n.2838-36C=) n.7151C= n.320C= n.364C= n.906C= c.2832C= (p.His944=) c.2745C= (p.His915=) c.1704C= (p.His568=) | |
17 | g.46032203G>T | CA399987070 | KANSL1 | c.2934C>A (p.His978Gln) c.2931C>A (p.His977Gln) c.2742C>A (p.His914Gln) n.882C>A c.591C>A (p.His197Gln) n.351C>A c.2838-36C>A (n.2838-36C>A) n.7151C>A n.320C>A n.364C>A n.906C>A c.2832C>A (p.His944Gln) c.2745C>A (p.His915Gln) c.1704C>A (p.His568Gln) | |
17 | g.46032204T>A | CA399987072 | KANSL1 | c.2933A>T (p.His978Leu) c.2930A>T (p.His977Leu) c.2741A>T (p.His914Leu) n.881A>T c.590A>T (p.His197Leu) n.350A>T c.2838-37A>T (n.2838-37A>T) n.7150A>T n.319A>T n.363A>T n.905A>T c.2831A>T (p.His944Leu) c.2744A>T (p.His915Leu) c.1703A>T (p.His568Leu) | dbSNP |
17 | g.46032204T>C | CA399987073 | KANSL1 | c.2933A>G (p.His978Arg) c.2930A>G (p.His977Arg) c.2741A>G (p.His914Arg) n.881A>G c.590A>G (p.His197Arg) n.350A>G c.2838-37A>G (n.2838-37A>G) n.7150A>G n.319A>G n.363A>G n.905A>G c.2831A>G (p.His944Arg) c.2744A>G (p.His915Arg) c.1703A>G (p.His568Arg) | |
17 | g.46032204T>G | CA399987074 | KANSL1 | c.2933A>C (p.His978Pro) c.2930A>C (p.His977Pro) c.2741A>C (p.His914Pro) n.881A>C c.590A>C (p.His197Pro) n.350A>C c.2838-37A>C (n.2838-37A>C) n.7150A>C n.319A>C n.363A>C n.905A>C c.2831A>C (p.His944Pro) c.2744A>C (p.His915Pro) c.1703A>C (p.His568Pro) | |
17 | g.46032204T= | CA2262111043 | KANSL1 | c.2933A= (p.His978=) c.2930A= (p.His977=) c.2741A= (p.His914=) n.881A= c.590A= (p.His197=) n.350A= c.2838-37A= (n.2838-37A=) n.7150A= n.319A= n.363A= n.905A= c.2831A= (p.His944=) c.2744A= (p.His915=) c.1703A= (p.His568=) | |
17 | g.46032205G>A | CA399987075 | KANSL1 | c.2932C>T (p.His978Tyr) c.2929C>T (p.His977Tyr) c.2740C>T (p.His914Tyr) n.880C>T c.589C>T (p.His197Tyr) n.349C>T c.2838-38C>T (n.2838-38C>T) n.7149C>T n.318C>T n.362C>T n.904C>T c.2830C>T (p.His944Tyr) c.2743C>T (p.His915Tyr) c.1702C>T (p.His568Tyr) | dbSNP gnomAD v4 |
17 | g.46032205G>C | CA399987077 | KANSL1 | c.2932C>G (p.His978Asp) c.2929C>G (p.His977Asp) c.2740C>G (p.His914Asp) n.880C>G c.589C>G (p.His197Asp) n.349C>G c.2838-38C>G (n.2838-38C>G) n.7149C>G n.318C>G n.362C>G n.904C>G c.2830C>G (p.His944Asp) c.2743C>G (p.His915Asp) c.1702C>G (p.His568Asp) | |
17 | g.46032205G= | CA2262111044 | KANSL1 | c.2932C= (p.His978=) c.2929C= (p.His977=) c.2740C= (p.His914=) n.880C= c.589C= (p.His197=) n.349C= c.2838-38C= (n.2838-38C=) n.7149C= n.318C= n.362C= n.904C= c.2830C= (p.His944=) c.2743C= (p.His915=) c.1702C= (p.His568=) | |
17 | g.46032205G>T | CA399987084 | KANSL1 | c.2932C>A (p.His978Asn) c.2929C>A (p.His977Asn) c.2740C>A (p.His914Asn) n.880C>A c.589C>A (p.His197Asn) n.349C>A c.2838-38C>A (n.2838-38C>A) n.7149C>A n.318C>A n.362C>A n.904C>A c.2830C>A (p.His944Asn) c.2743C>A (p.His915Asn) c.1702C>A (p.His568Asn) | |
17 | g.46032206G>A | CA500372022 | KANSL1 | c.2931C>T (p.Ser977=) c.2928C>T (p.Ser976=) c.2739C>T (p.Ser913=) n.879C>T c.588C>T (p.Ser196=) n.348C>T c.2838-39C>T (n.2838-39C>T) n.7148C>T n.317C>T n.361C>T n.903C>T c.2829C>T (p.Ser943=) c.2742C>T (p.Ser914=) c.1701C>T (p.Ser567=) | ClinVar dbSNP |
17 | g.46032206G>C | CA399987088 | KANSL1 | c.2931C>G (p.Ser977Arg) c.2928C>G (p.Ser976Arg) c.2739C>G (p.Ser913Arg) n.879C>G c.588C>G (p.Ser196Arg) n.348C>G c.2838-39C>G (n.2838-39C>G) n.7148C>G n.317C>G n.361C>G n.903C>G c.2829C>G (p.Ser943Arg) c.2742C>G (p.Ser914Arg) c.1701C>G (p.Ser567Arg) | |
17 | g.46032206G>T | CA399987089 | KANSL1 | c.2931C>A (p.Ser977Arg) c.2928C>A (p.Ser976Arg) c.2739C>A (p.Ser913Arg) n.879C>A c.588C>A (p.Ser196Arg) n.348C>A c.2838-39C>A (n.2838-39C>A) n.7148C>A n.317C>A n.361C>A n.903C>A c.2829C>A (p.Ser943Arg) c.2742C>A (p.Ser914Arg) c.1701C>A (p.Ser567Arg) | |
17 | g.46032207C>A | CA399987091 | KANSL1 | c.2930G>T (p.Ser977Ile) c.2927G>T (p.Ser976Ile) c.2738G>T (p.Ser913Ile) n.878G>T c.587G>T (p.Ser196Ile) n.347G>T c.2838-40G>T (n.2838-40G>T) n.7147G>T n.316G>T n.360G>T n.902G>T c.2828G>T (p.Ser943Ile) c.2741G>T (p.Ser914Ile) c.1700G>T (p.Ser567Ile) | |
17 | g.46032207C>G | CA399987093 | KANSL1 | c.2930G>C (p.Ser977Thr) c.2927G>C (p.Ser976Thr) c.2738G>C (p.Ser913Thr) n.878G>C c.587G>C (p.Ser196Thr) n.347G>C c.2838-40G>C (n.2838-40G>C) n.7147G>C n.316G>C n.360G>C n.902G>C c.2828G>C (p.Ser943Thr) c.2741G>C (p.Ser914Thr) c.1700G>C (p.Ser567Thr) | |
17 | g.46032207C>T | CA399987094 | KANSL1 | c.2930G>A (p.Ser977Asn) c.2927G>A (p.Ser976Asn) c.2738G>A (p.Ser913Asn) n.878G>A c.587G>A (p.Ser196Asn) n.347G>A c.2838-40G>A (n.2838-40G>A) n.7147G>A n.316G>A n.360G>A n.902G>A c.2828G>A (p.Ser943Asn) c.2741G>A (p.Ser914Asn) c.1700G>A (p.Ser567Asn) | gnomAD v4 |
17 | g.46032208T>A | CA399987101 | KANSL1 | c.2929A>T (p.Ser977Cys) c.2926A>T (p.Ser976Cys) c.2737A>T (p.Ser913Cys) n.877A>T c.586A>T (p.Ser196Cys) n.346A>T c.2838-41A>T (n.2838-41A>T) n.7146A>T n.315A>T n.359A>T n.901A>T c.2827A>T (p.Ser943Cys) c.2740A>T (p.Ser914Cys) c.1699A>T (p.Ser567Cys) | |
17 | g.46032208T>C | CA399987096 | KANSL1 | c.2929A>G (p.Ser977Gly) c.2926A>G (p.Ser976Gly) c.2737A>G (p.Ser913Gly) n.877A>G c.586A>G (p.Ser196Gly) n.346A>G c.2838-41A>G (n.2838-41A>G) n.7146A>G n.315A>G n.359A>G n.901A>G c.2827A>G (p.Ser943Gly) c.2740A>G (p.Ser914Gly) c.1699A>G (p.Ser567Gly) | gnomAD v4 |
17 | g.46032208T>G | CA399987099 | KANSL1 | c.2929A>C (p.Ser977Arg) c.2926A>C (p.Ser976Arg) c.2737A>C (p.Ser913Arg) n.877A>C c.586A>C (p.Ser196Arg) n.346A>C c.2838-41A>C (n.2838-41A>C) n.7146A>C n.315A>C n.359A>C n.901A>C c.2827A>C (p.Ser943Arg) c.2740A>C (p.Ser914Arg) c.1699A>C (p.Ser567Arg) | |
17 | g.46032209A>C | CA399987103 | KANSL1 | c.2928T>G (p.Ser976Arg) c.2925T>G (p.Ser975Arg) c.2736T>G (p.Ser912Arg) n.876T>G c.585T>G (p.Ser195Arg) n.345T>G c.2838-42T>G (n.2838-42T>G) n.7145T>G n.314T>G n.358T>G n.900T>G c.2826T>G (p.Ser942Arg) c.2739T>G (p.Ser913Arg) c.1698T>G (p.Ser566Arg) | |
17 | g.46032209A>G | CA500372023 | KANSL1 | c.2928T>C (p.Ser976=) c.2925T>C (p.Ser975=) c.2736T>C (p.Ser912=) n.876T>C c.585T>C (p.Ser195=) n.345T>C c.2838-42T>C (n.2838-42T>C) n.7145T>C n.314T>C n.358T>C n.900T>C c.2826T>C (p.Ser942=) c.2739T>C (p.Ser913=) c.1698T>C (p.Ser566=) | |
17 | g.46032209A>T | CA399987104 | KANSL1 | c.2928T>A (p.Ser976Arg) c.2925T>A (p.Ser975Arg) c.2736T>A (p.Ser912Arg) n.876T>A c.585T>A (p.Ser195Arg) n.345T>A c.2838-42T>A (n.2838-42T>A) n.7145T>A n.314T>A n.358T>A n.900T>A c.2826T>A (p.Ser942Arg) c.2739T>A (p.Ser913Arg) c.1698T>A (p.Ser566Arg) | |
17 | g.46032210C>A | CA8618414 | KANSL1 | c.2927G>T (p.Ser976Ile) c.2924G>T (p.Ser975Ile) c.2735G>T (p.Ser912Ile) n.875G>T c.584G>T (p.Ser195Ile) n.344G>T c.2838-43G>T (n.2838-43G>T) n.7144G>T n.313G>T n.357G>T n.899G>T c.2825G>T (p.Ser942Ile) c.2738G>T (p.Ser913Ile) c.1697G>T (p.Ser566Ile) | dbSNP ExAC gnomAD v2 |
17 | g.46032210C= | CA2262111045 | KANSL1 | c.2927G= (p.Ser976=) c.2924G= (p.Ser975=) c.2735G= (p.Ser912=) n.875G= c.584G= (p.Ser195=) n.344G= c.2838-43G= (n.2838-43G=) n.7144G= n.313G= n.357G= n.899G= c.2825G= (p.Ser942=) c.2738G= (p.Ser913=) c.1697G= (p.Ser566=) | |
17 | g.46032210C>G | CA399987106 | KANSL1 | c.2927G>C (p.Ser976Thr) c.2924G>C (p.Ser975Thr) c.2735G>C (p.Ser912Thr) n.875G>C c.584G>C (p.Ser195Thr) n.344G>C c.2838-43G>C (n.2838-43G>C) n.7144G>C n.313G>C n.357G>C n.899G>C c.2825G>C (p.Ser942Thr) c.2738G>C (p.Ser913Thr) c.1697G>C (p.Ser566Thr) | |
17 | g.46032210C>T | CA399987108 | KANSL1 | c.2927G>A (p.Ser976Asn) c.2924G>A (p.Ser975Asn) c.2735G>A (p.Ser912Asn) n.875G>A c.584G>A (p.Ser195Asn) n.344G>A c.2838-43G>A (n.2838-43G>A) n.7144G>A n.313G>A n.357G>A n.899G>A c.2825G>A (p.Ser942Asn) c.2738G>A (p.Ser913Asn) c.1697G>A (p.Ser566Asn) | gnomAD v4 |
17 | g.46032211T>A | CA8618415 | KANSL1 | c.2926A>T (p.Ser976Cys) c.2923A>T (p.Ser975Cys) c.2734A>T (p.Ser912Cys) n.874A>T c.583A>T (p.Ser195Cys) n.343A>T c.2838-44A>T (n.2838-44A>T) n.7143A>T n.312A>T n.356A>T n.898A>T c.2824A>T (p.Ser942Cys) c.2737A>T (p.Ser913Cys) c.1696A>T (p.Ser566Cys) | dbSNP ExAC gnomAD v2 |
17 | g.46032211T>C | CA399987112 | KANSL1 | c.2926A>G (p.Ser976Gly) c.2923A>G (p.Ser975Gly) c.2734A>G (p.Ser912Gly) n.874A>G c.583A>G (p.Ser195Gly) n.343A>G c.2838-44A>G (n.2838-44A>G) n.7143A>G n.312A>G n.356A>G n.898A>G c.2824A>G (p.Ser942Gly) c.2737A>G (p.Ser913Gly) c.1696A>G (p.Ser566Gly) | gnomAD v4 |
17 | g.46032211T>G | CA399987113 | KANSL1 | c.2926A>C (p.Ser976Arg) c.2923A>C (p.Ser975Arg) c.2734A>C (p.Ser912Arg) n.874A>C c.583A>C (p.Ser195Arg) n.343A>C c.2838-44A>C (n.2838-44A>C) n.7143A>C n.312A>C n.356A>C n.898A>C c.2824A>C (p.Ser942Arg) c.2737A>C (p.Ser913Arg) c.1696A>C (p.Ser566Arg) | |
17 | g.46032211T= | CA2262111046 | KANSL1 | c.2926A= (p.Ser976=) c.2923A= (p.Ser975=) c.2734A= (p.Ser912=) n.874A= c.583A= (p.Ser195=) n.343A= c.2838-44A= (n.2838-44A=) n.7143A= n.312A= n.356A= n.898A= c.2824A= (p.Ser942=) c.2737A= (p.Ser913=) c.1696A= (p.Ser566=) | |
17 | g.46032212G>A | CA8618416 | KANSL1 | c.2925C>T (p.Ser975=) c.2922C>T (p.Ser974=) c.2733C>T (p.Ser911=) n.873C>T c.582C>T (p.Ser194=) n.342C>T c.2838-45C>T (n.2838-45C>T) n.7142C>T n.311C>T n.355C>T n.897C>T c.2823C>T (p.Ser941=) c.2736C>T (p.Ser912=) c.1695C>T (p.Ser565=) | dbSNP ExAC gnomAD v2 |
17 | g.46032212G>C | CA399987116 | KANSL1 | c.2925C>G (p.Ser975Arg) c.2922C>G (p.Ser974Arg) c.2733C>G (p.Ser911Arg) n.873C>G c.582C>G (p.Ser194Arg) n.342C>G c.2838-45C>G (n.2838-45C>G) n.7142C>G n.311C>G n.355C>G n.897C>G c.2823C>G (p.Ser941Arg) c.2736C>G (p.Ser912Arg) c.1695C>G (p.Ser565Arg) | |
17 | g.46032212G= | CA2262111047 | KANSL1 | c.2925C= (p.Ser975=) c.2922C= (p.Ser974=) c.2733C= (p.Ser911=) n.873C= c.582C= (p.Ser194=) n.342C= c.2838-45C= (n.2838-45C=) n.7142C= n.311C= n.355C= n.897C= c.2823C= (p.Ser941=) c.2736C= (p.Ser912=) c.1695C= (p.Ser565=) | |
17 | g.46032212G>T | CA399987118 | KANSL1 | c.2925C>A (p.Ser975Arg) c.2922C>A (p.Ser974Arg) c.2733C>A (p.Ser911Arg) n.873C>A c.582C>A (p.Ser194Arg) n.342C>A c.2838-45C>A (n.2838-45C>A) n.7142C>A n.311C>A n.355C>A n.897C>A c.2823C>A (p.Ser941Arg) c.2736C>A (p.Ser912Arg) c.1695C>A (p.Ser565Arg) | |
17 | g.46032213C>A | CA399987122 | KANSL1 | c.2924G>T (p.Ser975Ile) c.2921G>T (p.Ser974Ile) c.2732G>T (p.Ser911Ile) n.872G>T c.581G>T (p.Ser194Ile) n.341G>T c.2838-46G>T (n.2838-46G>T) n.7141G>T n.310G>T n.354G>T n.896G>T c.2822G>T (p.Ser941Ile) c.2735G>T (p.Ser912Ile) c.1694G>T (p.Ser565Ile) | gnomAD v4 |
17 | g.46032213C>G | CA399987123 | KANSL1 | c.2924G>C (p.Ser975Thr) c.2921G>C (p.Ser974Thr) c.2732G>C (p.Ser911Thr) n.872G>C c.581G>C (p.Ser194Thr) n.341G>C c.2838-46G>C (n.2838-46G>C) n.7141G>C n.310G>C n.354G>C n.896G>C c.2822G>C (p.Ser941Thr) c.2735G>C (p.Ser912Thr) c.1694G>C (p.Ser565Thr) | |
17 | g.46032213C>T | CA399987120 | KANSL1 | c.2924G>A (p.Ser975Asn) c.2921G>A (p.Ser974Asn) c.2732G>A (p.Ser911Asn) n.872G>A c.581G>A (p.Ser194Asn) n.341G>A c.2838-46G>A (n.2838-46G>A) n.7141G>A n.310G>A n.354G>A n.896G>A c.2822G>A (p.Ser941Asn) c.2735G>A (p.Ser912Asn) c.1694G>A (p.Ser565Asn) | |
17 | g.46032214T>A | CA399987125 | KANSL1 | c.2923A>T (p.Ser975Cys) c.2920A>T (p.Ser974Cys) c.2731A>T (p.Ser911Cys) n.871A>T c.580A>T (p.Ser194Cys) n.340A>T c.2838-47A>T (n.2838-47A>T) n.7140A>T n.309A>T n.353A>T n.895A>T c.2821A>T (p.Ser941Cys) c.2734A>T (p.Ser912Cys) c.1693A>T (p.Ser565Cys) | |
17 | g.46032214T>C | CA399987127 | KANSL1 | c.2923A>G (p.Ser975Gly) c.2920A>G (p.Ser974Gly) c.2731A>G (p.Ser911Gly) n.871A>G c.580A>G (p.Ser194Gly) n.340A>G c.2838-47A>G (n.2838-47A>G) n.7140A>G n.309A>G n.353A>G n.895A>G c.2821A>G (p.Ser941Gly) c.2734A>G (p.Ser912Gly) c.1693A>G (p.Ser565Gly) | |
17 | g.46032214T>G | CA399987129 | KANSL1 | c.2923A>C (p.Ser975Arg) c.2920A>C (p.Ser974Arg) c.2731A>C (p.Ser911Arg) n.871A>C c.580A>C (p.Ser194Arg) n.340A>C c.2838-47A>C (n.2838-47A>C) n.7140A>C n.309A>C n.353A>C n.895A>C c.2821A>C (p.Ser941Arg) c.2734A>C (p.Ser912Arg) c.1693A>C (p.Ser565Arg) | |
17 | g.46032215G>A | CA500372025 | KANSL1 | c.2922C>T (p.Val974=) c.2919C>T (p.Val973=) c.2730C>T (p.Val910=) n.870C>T c.579C>T (p.Val193=) n.339C>T c.2838-48C>T (n.2838-48C>T) n.7139C>T n.308C>T n.352C>T n.894C>T c.2820C>T (p.Val940=) c.2733C>T (p.Val911=) c.1692C>T (p.Val564=) | |
17 | g.46032215G>C | CA500372026 | KANSL1 | c.2922C>G (p.Val974=) c.2919C>G (p.Val973=) c.2730C>G (p.Val910=) n.870C>G c.579C>G (p.Val193=) n.339C>G c.2838-48C>G (n.2838-48C>G) n.7139C>G n.308C>G n.352C>G n.894C>G c.2820C>G (p.Val940=) c.2733C>G (p.Val911=) c.1692C>G (p.Val564=) | |
17 | g.46032215G>T | CA500372024 | KANSL1 | c.2922C>A (p.Val974=) c.2919C>A (p.Val973=) c.2730C>A (p.Val910=) n.870C>A c.579C>A (p.Val193=) n.339C>A c.2838-48C>A (n.2838-48C>A) n.7139C>A n.308C>A n.352C>A n.894C>A c.2820C>A (p.Val940=) c.2733C>A (p.Val911=) c.1692C>A (p.Val564=) | |
17 | g.46032216A>C | CA399987131 | KANSL1 | c.2921T>G (p.Val974Gly) c.2918T>G (p.Val973Gly) c.2729T>G (p.Val910Gly) n.869T>G c.578T>G (p.Val193Gly) n.338T>G c.2838-49T>G (n.2838-49T>G) n.7138T>G n.307T>G n.351T>G n.893T>G c.2819T>G (p.Val940Gly) c.2732T>G (p.Val911Gly) c.1691T>G (p.Val564Gly) | |
17 | g.46032216A>G | CA399987133 | KANSL1 | c.2921T>C (p.Val974Ala) c.2918T>C (p.Val973Ala) c.2729T>C (p.Val910Ala) n.869T>C c.578T>C (p.Val193Ala) n.338T>C c.2838-49T>C (n.2838-49T>C) n.7138T>C n.307T>C n.351T>C n.893T>C c.2819T>C (p.Val940Ala) c.2732T>C (p.Val911Ala) c.1691T>C (p.Val564Ala) | |
17 | g.46032216A>T | CA399987135 | KANSL1 | c.2921T>A (p.Val974Asp) c.2918T>A (p.Val973Asp) c.2729T>A (p.Val910Asp) n.869T>A c.578T>A (p.Val193Asp) n.338T>A c.2838-49T>A (n.2838-49T>A) n.7138T>A n.307T>A n.351T>A n.893T>A c.2819T>A (p.Val940Asp) c.2732T>A (p.Val911Asp) c.1691T>A (p.Val564Asp) | |
17 | g.46032217C>A | CA399987137 | KANSL1 | c.2920G>T (p.Val974Phe) c.2917G>T (p.Val973Phe) c.2728G>T (p.Val910Phe) n.868G>T c.577G>T (p.Val193Phe) n.337G>T c.2838-50G>T (n.2838-50G>T) n.7137G>T n.306G>T n.350G>T n.892G>T c.2818G>T (p.Val940Phe) c.2731G>T (p.Val911Phe) c.1690G>T (p.Val564Phe) | |
17 | g.46032217C>G | CA399987138 | KANSL1 | c.2920G>C (p.Val974Leu) c.2917G>C (p.Val973Leu) c.2728G>C (p.Val910Leu) n.868G>C c.577G>C (p.Val193Leu) n.337G>C c.2838-50G>C (n.2838-50G>C) n.7137G>C n.306G>C n.350G>C n.892G>C c.2818G>C (p.Val940Leu) c.2731G>C (p.Val911Leu) c.1690G>C (p.Val564Leu) | |
17 | g.46032217C>T | CA399987139 | KANSL1 | c.2920G>A (p.Val974Ile) c.2917G>A (p.Val973Ile) c.2728G>A (p.Val910Ile) n.868G>A c.577G>A (p.Val193Ile) n.337G>A c.2838-50G>A (n.2838-50G>A) n.7137G>A n.306G>A n.350G>A n.892G>A c.2818G>A (p.Val940Ile) c.2731G>A (p.Val911Ile) c.1690G>A (p.Val564Ile) | |
17 | g.46032218A= | CA2262111048 | KANSL1 | c.2919T= (p.Asp973=) c.2916T= (p.Asp972=) c.2727T= (p.Asp909=) n.867T= c.576T= (p.Asp192=) n.336T= c.2838-51T= (n.2838-51T=) n.7136T= n.305T= n.349T= n.891T= c.2817T= (p.Asp939=) c.2730T= (p.Asp910=) c.1689T= (p.Asp563=) | |
17 | g.46032218A>C | CA8618417 | KANSL1 | c.2919T>G (p.Asp973Glu) c.2916T>G (p.Asp972Glu) c.2727T>G (p.Asp909Glu) n.867T>G c.576T>G (p.Asp192Glu) n.336T>G c.2838-51T>G (n.2838-51T>G) n.7136T>G n.305T>G n.349T>G n.891T>G c.2817T>G (p.Asp939Glu) c.2730T>G (p.Asp910Glu) c.1689T>G (p.Asp563Glu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.46032218A>G | CA500372028 | KANSL1 | c.2919T>C (p.Asp973=) c.2916T>C (p.Asp972=) c.2727T>C (p.Asp909=) n.867T>C c.576T>C (p.Asp192=) n.336T>C c.2838-51T>C (n.2838-51T>C) n.7136T>C n.305T>C n.349T>C n.891T>C c.2817T>C (p.Asp939=) c.2730T>C (p.Asp910=) c.1689T>C (p.Asp563=) | ClinVar |
17 | g.46032218A>T | CA399987142 | KANSL1 | c.2919T>A (p.Asp973Glu) c.2916T>A (p.Asp972Glu) c.2727T>A (p.Asp909Glu) n.867T>A c.576T>A (p.Asp192Glu) n.336T>A c.2838-51T>A (n.2838-51T>A) n.7136T>A n.305T>A n.349T>A n.891T>A c.2817T>A (p.Asp939Glu) c.2730T>A (p.Asp910Glu) c.1689T>A (p.Asp563Glu) | |
17 | g.46032219T>A | CA399987146 | KANSL1 | c.2918A>T (p.Asp973Val) c.2915A>T (p.Asp972Val) c.2726A>T (p.Asp909Val) n.866A>T c.575A>T (p.Asp192Val) n.335A>T c.2838-52A>T (n.2838-52A>T) n.7135A>T n.304A>T n.348A>T n.890A>T c.2816A>T (p.Asp939Val) c.2729A>T (p.Asp910Val) c.1688A>T (p.Asp563Val) | |
17 | g.46032219T>C | CA399987152 | KANSL1 | c.2918A>G (p.Asp973Gly) c.2915A>G (p.Asp972Gly) c.2726A>G (p.Asp909Gly) n.866A>G c.575A>G (p.Asp192Gly) n.335A>G c.2838-52A>G (n.2838-52A>G) n.7135A>G n.304A>G n.348A>G n.890A>G c.2816A>G (p.Asp939Gly) c.2729A>G (p.Asp910Gly) c.1688A>G (p.Asp563Gly) | |
17 | g.46032219T>G | CA399987144 | KANSL1 | c.2918A>C (p.Asp973Ala) c.2915A>C (p.Asp972Ala) c.2726A>C (p.Asp909Ala) n.866A>C c.575A>C (p.Asp192Ala) n.335A>C c.2838-52A>C (n.2838-52A>C) n.7135A>C n.304A>C n.348A>C n.890A>C c.2816A>C (p.Asp939Ala) c.2729A>C (p.Asp910Ala) c.1688A>C (p.Asp563Ala) | |
17 | g.46032220C>A | CA399987154 | KANSL1 | c.2917G>T (p.Asp973Tyr) c.2914G>T (p.Asp972Tyr) c.2725G>T (p.Asp909Tyr) n.745G>T n.865G>T c.574G>T (p.Asp192Tyr) n.334G>T c.2838-53G>T (n.2838-53G>T) n.7134G>T n.303G>T n.347G>T n.889G>T c.2815G>T (p.Asp939Tyr) c.2728G>T (p.Asp910Tyr) c.1687G>T (p.Asp563Tyr) | gnomAD v4 |
17 | g.46032220C>G | CA399987156 | KANSL1 | c.2917G>C (p.Asp973His) c.2914G>C (p.Asp972His) c.2725G>C (p.Asp909His) n.745G>C n.865G>C c.574G>C (p.Asp192His) n.334G>C c.2838-53G>C (n.2838-53G>C) n.7134G>C n.303G>C n.347G>C n.889G>C c.2815G>C (p.Asp939His) c.2728G>C (p.Asp910His) c.1687G>C (p.Asp563His) | |
17 | g.46032220C>T | CA399987157 | KANSL1 | c.2917G>A (p.Asp973Asn) c.2914G>A (p.Asp972Asn) c.2725G>A (p.Asp909Asn) n.745G>A n.865G>A c.574G>A (p.Asp192Asn) n.334G>A c.2838-53G>A (n.2838-53G>A) n.7134G>A n.303G>A n.347G>A n.889G>A c.2815G>A (p.Asp939Asn) c.2728G>A (p.Asp910Asn) c.1687G>A (p.Asp563Asn) | |
17 | g.46032221A>C | CA500372030 | KANSL1 | c.2916T>G (p.Pro972=) c.2913T>G (p.Pro971=) c.2724T>G (p.Pro908=) n.744T>G n.864T>G c.573T>G (p.Pro191=) n.333T>G c.2838-54T>G (n.2838-54T>G) n.7133T>G n.302T>G n.346T>G n.888T>G c.2814T>G (p.Pro938=) c.2727T>G (p.Pro909=) c.1686T>G (p.Pro562=) | |
17 | g.46032221A>G | CA500372029 | KANSL1 | c.2916T>C (p.Pro972=) c.2913T>C (p.Pro971=) c.2724T>C (p.Pro908=) n.744T>C n.864T>C c.573T>C (p.Pro191=) n.333T>C c.2838-54T>C (n.2838-54T>C) n.7133T>C n.302T>C n.346T>C n.888T>C c.2814T>C (p.Pro938=) c.2727T>C (p.Pro909=) c.1686T>C (p.Pro562=) | ClinVar |
17 | g.46032221A>T | CA500372031 | KANSL1 | c.2916T>A (p.Pro972=) c.2913T>A (p.Pro971=) c.2724T>A (p.Pro908=) n.744T>A n.864T>A c.573T>A (p.Pro191=) n.333T>A c.2838-54T>A (n.2838-54T>A) n.7133T>A n.302T>A n.346T>A n.888T>A c.2814T>A (p.Pro938=) c.2727T>A (p.Pro909=) c.1686T>A (p.Pro562=) | |
17 | g.46032222G>A | CA399987159 | KANSL1 | c.2915C>T (p.Pro972Leu) c.2912C>T (p.Pro971Leu) c.2723C>T (p.Pro908Leu) n.743C>T n.863C>T c.572C>T (p.Pro191Leu) n.332C>T c.2838-55C>T (n.2838-55C>T) n.7132C>T n.301C>T n.345C>T n.887C>T c.2813C>T (p.Pro938Leu) c.2726C>T (p.Pro909Leu) c.1685C>T (p.Pro562Leu) | gnomAD v4 |
17 | g.46032222G>C | CA399987161 | KANSL1 | c.2915C>G (p.Pro972Arg) c.2912C>G (p.Pro971Arg) c.2723C>G (p.Pro908Arg) n.743C>G n.863C>G c.572C>G (p.Pro191Arg) n.332C>G c.2838-55C>G (n.2838-55C>G) n.7132C>G n.301C>G n.345C>G n.887C>G c.2813C>G (p.Pro938Arg) c.2726C>G (p.Pro909Arg) c.1685C>G (p.Pro562Arg) | |
17 | g.46032222G>T | CA399987162 | KANSL1 | c.2915C>A (p.Pro972His) c.2912C>A (p.Pro971His) c.2723C>A (p.Pro908His) n.743C>A n.863C>A c.572C>A (p.Pro191His) n.332C>A c.2838-55C>A (n.2838-55C>A) n.7132C>A n.301C>A n.345C>A n.887C>A c.2813C>A (p.Pro938His) c.2726C>A (p.Pro909His) c.1685C>A (p.Pro562His) | |
17 | g.46032223G>A | CA399987166 | KANSL1 | c.2914C>T (p.Pro972Ser) c.2911C>T (p.Pro971Ser) c.2722C>T (p.Pro908Ser) n.742C>T n.862C>T c.571C>T (p.Pro191Ser) n.331C>T c.2838-56C>T (n.2838-56C>T) n.7131C>T n.300C>T n.344C>T n.886C>T c.2812C>T (p.Pro938Ser) c.2725C>T (p.Pro909Ser) c.1684C>T (p.Pro562Ser) | |
17 | g.46032223G>C | CA399987169 | KANSL1 | c.2914C>G (p.Pro972Ala) c.2911C>G (p.Pro971Ala) c.2722C>G (p.Pro908Ala) n.742C>G n.862C>G c.571C>G (p.Pro191Ala) n.331C>G c.2838-56C>G (n.2838-56C>G) n.7131C>G n.300C>G n.344C>G n.886C>G c.2812C>G (p.Pro938Ala) c.2725C>G (p.Pro909Ala) c.1684C>G (p.Pro562Ala) | |
17 | g.46032223G>T | CA399987167 | KANSL1 | c.2914C>A (p.Pro972Thr) c.2911C>A (p.Pro971Thr) c.2722C>A (p.Pro908Thr) n.742C>A n.862C>A c.571C>A (p.Pro191Thr) n.331C>A c.2838-56C>A (n.2838-56C>A) n.7131C>A n.300C>A n.344C>A n.886C>A c.2812C>A (p.Pro938Thr) c.2725C>A (p.Pro909Thr) c.1684C>A (p.Pro562Thr) | |
17 | g.46032224G>A | CA500372032 | KANSL1 | c.2913C>T (p.Ser971=) c.2910C>T (p.Ser970=) c.2721C>T (p.Ser907=) n.741C>T n.861C>T c.570C>T (p.Ser190=) n.330C>T c.2838-57C>T (n.2838-57C>T) n.7130C>T n.299C>T n.343C>T n.885C>T c.2811C>T (p.Ser937=) c.2724C>T (p.Ser908=) c.1683C>T (p.Ser561=) | dbSNP gnomAD v2 |
17 | g.46032224G>C | CA500372033 | KANSL1 | c.2913C>G (p.Ser971=) c.2910C>G (p.Ser970=) c.2721C>G (p.Ser907=) n.741C>G n.861C>G c.570C>G (p.Ser190=) n.330C>G c.2838-57C>G (n.2838-57C>G) n.7130C>G n.299C>G n.343C>G n.885C>G c.2811C>G (p.Ser937=) c.2724C>G (p.Ser908=) c.1683C>G (p.Ser561=) | |
17 | g.46032224G= | CA2262111049 | KANSL1 | c.2913C= (p.Ser971=) c.2910C= (p.Ser970=) c.2721C= (p.Ser907=) n.741C= n.861C= c.570C= (p.Ser190=) n.330C= c.2838-57C= (n.2838-57C=) n.7130C= n.299C= n.343C= n.885C= c.2811C= (p.Ser937=) c.2724C= (p.Ser908=) c.1683C= (p.Ser561=) | |
17 | g.46032224G>T | CA8618418 | KANSL1 | c.2913C>A (p.Ser971=) c.2910C>A (p.Ser970=) c.2721C>A (p.Ser907=) n.741C>A n.861C>A c.570C>A (p.Ser190=) n.330C>A c.2838-57C>A (n.2838-57C>A) n.7130C>A n.299C>A n.343C>A n.885C>A c.2811C>A (p.Ser937=) c.2724C>A (p.Ser908=) c.1683C>A (p.Ser561=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.46032225G>A | CA399987171 | KANSL1 | c.2912C>T (p.Ser971Phe) c.2909C>T (p.Ser970Phe) c.2720C>T (p.Ser907Phe) n.740C>T n.860C>T c.569C>T (p.Ser190Phe) n.329C>T c.2838-58C>T (n.2838-58C>T) n.7129C>T n.298C>T n.342C>T n.884C>T c.2810C>T (p.Ser937Phe) c.2723C>T (p.Ser908Phe) c.1682C>T (p.Ser561Phe) | dbSNP |
17 | g.46032225G>C | CA399987172 | KANSL1 | c.2912C>G (p.Ser971Cys) c.2909C>G (p.Ser970Cys) c.2720C>G (p.Ser907Cys) n.740C>G n.860C>G c.569C>G (p.Ser190Cys) n.329C>G c.2838-58C>G (n.2838-58C>G) n.7129C>G n.298C>G n.342C>G n.884C>G c.2810C>G (p.Ser937Cys) c.2723C>G (p.Ser908Cys) c.1682C>G (p.Ser561Cys) | |
17 | g.46032225G= | CA2262111050 | KANSL1 | c.2912C= (p.Ser971=) c.2909C= (p.Ser970=) c.2720C= (p.Ser907=) n.740C= n.860C= c.569C= (p.Ser190=) n.329C= c.2838-58C= (n.2838-58C=) n.7129C= n.298C= n.342C= n.884C= c.2810C= (p.Ser937=) c.2723C= (p.Ser908=) c.1682C= (p.Ser561=) | |
17 | g.46032225G>T | CA399987173 | KANSL1 | c.2912C>A (p.Ser971Tyr) c.2909C>A (p.Ser970Tyr) c.2720C>A (p.Ser907Tyr) n.740C>A n.860C>A c.569C>A (p.Ser190Tyr) n.329C>A c.2838-58C>A (n.2838-58C>A) n.7129C>A n.298C>A n.342C>A n.884C>A c.2810C>A (p.Ser937Tyr) c.2723C>A (p.Ser908Tyr) c.1682C>A (p.Ser561Tyr) | gnomAD v4 |
17 | g.46032226A= | CA2262111051 | KANSL1 | c.2911T= (p.Ser971=) c.2908T= (p.Ser970=) c.2719T= (p.Ser907=) n.739T= n.859T= c.568T= (p.Ser190=) n.328T= c.2838-59T= (n.2838-59T=) n.7128T= n.297T= n.341T= n.883T= c.2809T= (p.Ser937=) c.2722T= (p.Ser908=) c.1681T= (p.Ser561=) | |
17 | g.46032226A>C | CA399987178 | KANSL1 | c.2911T>G (p.Ser971Ala) c.2908T>G (p.Ser970Ala) c.2719T>G (p.Ser907Ala) n.739T>G n.859T>G c.568T>G (p.Ser190Ala) n.328T>G c.2838-59T>G (n.2838-59T>G) n.7128T>G n.297T>G n.341T>G n.883T>G c.2809T>G (p.Ser937Ala) c.2722T>G (p.Ser908Ala) c.1681T>G (p.Ser561Ala) | |
17 | g.46032226A>G | CA399987177 | KANSL1 | c.2911T>C (p.Ser971Pro) c.2908T>C (p.Ser970Pro) c.2719T>C (p.Ser907Pro) n.739T>C n.859T>C c.568T>C (p.Ser190Pro) n.328T>C c.2838-59T>C (n.2838-59T>C) n.7128T>C n.297T>C n.341T>C n.883T>C c.2809T>C (p.Ser937Pro) c.2722T>C (p.Ser908Pro) c.1681T>C (p.Ser561Pro) | |
17 | g.46032226A>T | CA399987175 | KANSL1 | c.2911T>A (p.Ser971Thr) c.2908T>A (p.Ser970Thr) c.2719T>A (p.Ser907Thr) n.739T>A n.859T>A c.568T>A (p.Ser190Thr) n.328T>A c.2838-59T>A (n.2838-59T>A) n.7128T>A n.297T>A n.341T>A n.883T>A c.2809T>A (p.Ser937Thr) c.2722T>A (p.Ser908Thr) c.1681T>A (p.Ser561Thr) | dbSNP gnomAD v2 gnomAD v4 |