| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.113388988A>C | CA374562921 | ALAD | c.920T>G (p.Phe307Cys) n.1193T>G c.1007T>G (p.Phe336Cys) c.1046T>G (p.Phe349Cys) c.947T>G (p.Phe316Cys) c.896T>G (p.Phe299Cys) | |
| 9 | g.113388988A>G | CA374562923 | ALAD | c.920T>C (p.Phe307Ser) n.1193T>C c.1007T>C (p.Phe336Ser) c.1046T>C (p.Phe349Ser) c.947T>C (p.Phe316Ser) c.896T>C (p.Phe299Ser) | |
| 9 | g.113388988A>T | CA374562922 | ALAD | c.920T>A (p.Phe307Tyr) n.1193T>A c.1007T>A (p.Phe336Tyr) c.1046T>A (p.Phe349Tyr) c.947T>A (p.Phe316Tyr) c.896T>A (p.Phe299Tyr) | |
| 9 | g.113388989A= | CA1873365572 | ALAD | c.919T= (p.Phe307=) n.1192T= c.1006T= (p.Phe336=) c.1045T= (p.Phe349=) c.946T= (p.Phe316=) c.895T= (p.Phe299=) | |
| 9 | g.113388989A>C | CA374562924 | ALAD | c.919T>G (p.Phe307Val) n.1192T>G c.1006T>G (p.Phe336Val) c.1045T>G (p.Phe349Val) c.946T>G (p.Phe316Val) c.895T>G (p.Phe299Val) | |
| 9 | g.113388989A>G | CA5196316 | ALAD | c.919T>C (p.Phe307Leu) n.1192T>C c.1006T>C (p.Phe336Leu) c.1045T>C (p.Phe349Leu) c.946T>C (p.Phe316Leu) c.895T>C (p.Phe299Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.113388989A>T | CA374562925 | ALAD | c.919T>A (p.Phe307Ile) n.1192T>A c.1006T>A (p.Phe336Ile) c.1045T>A (p.Phe349Ile) c.946T>A (p.Phe316Ile) c.895T>A (p.Phe299Ile) | |
| 9 | g.113388990G>A | CA466754838 | ALAD | c.918C>T (p.Ala306=) n.1191C>T c.1005C>T (p.Ala335=) c.1044C>T (p.Ala348=) c.945C>T (p.Ala315=) c.894C>T (p.Ala298=) | |
| 9 | g.113388990G>C | CA466754843 | ALAD | c.918C>G (p.Ala306=) n.1191C>G c.1005C>G (p.Ala335=) c.1044C>G (p.Ala348=) c.945C>G (p.Ala315=) c.894C>G (p.Ala298=) | |
| 9 | g.113388990G>T | CA466754845 | ALAD | c.918C>A (p.Ala306=) n.1191C>A c.1005C>A (p.Ala335=) c.1044C>A (p.Ala348=) c.945C>A (p.Ala315=) c.894C>A (p.Ala298=) | |
| 9 | g.113388991G>A | CA374562926 | ALAD | c.917C>T (p.Ala306Val) n.1190C>T c.1004C>T (p.Ala335Val) c.1043C>T (p.Ala348Val) c.944C>T (p.Ala315Val) c.893C>T (p.Ala298Val) | |
| 9 | g.113388991G>C | CA374562927 | ALAD | c.917C>G (p.Ala306Gly) n.1190C>G c.1004C>G (p.Ala335Gly) c.1043C>G (p.Ala348Gly) c.944C>G (p.Ala315Gly) c.893C>G (p.Ala298Gly) | |
| 9 | g.113388991G>T | CA374562928 | ALAD | c.917C>A (p.Ala306Asp) n.1190C>A c.1004C>A (p.Ala335Asp) c.1043C>A (p.Ala348Asp) c.944C>A (p.Ala315Asp) c.893C>A (p.Ala298Asp) | gnomAD v4 |
| 9 | g.113388992C>A | CA374562929 | ALAD | c.916G>T (p.Ala306Ser) n.1189G>T c.1003G>T (p.Ala335Ser) c.1042G>T (p.Ala348Ser) c.943G>T (p.Ala315Ser) c.892G>T (p.Ala298Ser) | |
| 9 | g.113388992C>G | CA374562930 | ALAD | c.916G>C (p.Ala306Pro) n.1189G>C c.1003G>C (p.Ala335Pro) c.1042G>C (p.Ala348Pro) c.943G>C (p.Ala315Pro) c.892G>C (p.Ala298Pro) | |
| 9 | g.113388992C>T | CA374562931 | ALAD | c.916G>A (p.Ala306Thr) n.1189G>A c.1003G>A (p.Ala335Thr) c.1042G>A (p.Ala348Thr) c.943G>A (p.Ala315Thr) c.892G>A (p.Ala298Thr) | |
| 9 | g.113388993A>C | CA466754855 | ALAD | c.915T>G (p.Thr305=) n.1188T>G c.1002T>G (p.Thr334=) c.1041T>G (p.Thr347=) c.942T>G (p.Thr314=) c.891T>G (p.Thr297=) | |
| 9 | g.113388993A>G | CA466754856 | ALAD | c.915T>C (p.Thr305=) n.1188T>C c.1002T>C (p.Thr334=) c.1041T>C (p.Thr347=) c.942T>C (p.Thr314=) c.891T>C (p.Thr297=) | |
| 9 | g.113388993A>T | CA466754859 | ALAD | c.915T>A (p.Thr305=) n.1188T>A c.1002T>A (p.Thr334=) c.1041T>A (p.Thr347=) c.942T>A (p.Thr314=) c.891T>A (p.Thr297=) | |
| 9 | g.113388994G>A | CA198545521 | ALAD | c.914C>T (p.Thr305Ile) n.1187C>T c.1001C>T (p.Thr334Ile) c.1040C>T (p.Thr347Ile) c.941C>T (p.Thr314Ile) c.890C>T (p.Thr297Ile) | dbSNP |
| 9 | g.113388994G>C | CA374562932 | ALAD | c.914C>G (p.Thr305Ser) n.1187C>G c.1001C>G (p.Thr334Ser) c.1040C>G (p.Thr347Ser) c.941C>G (p.Thr314Ser) c.890C>G (p.Thr297Ser) | dbSNP gnomAD v4 |
| 9 | g.113388994G= | CA1873365573 | ALAD | c.914C= (p.Thr305=) n.1187C= c.1001C= (p.Thr334=) c.1040C= (p.Thr347=) c.941C= (p.Thr314=) c.890C= (p.Thr297=) | |
| 9 | g.113388994G>T | CA374562933 | ALAD | c.914C>A (p.Thr305Asn) n.1187C>A c.1001C>A (p.Thr334Asn) c.1040C>A (p.Thr347Asn) c.941C>A (p.Thr314Asn) c.890C>A (p.Thr297Asn) | |
| 9 | g.113388995T>A | CA374562934 | ALAD | c.913A>T (p.Thr305Ser) n.1186A>T c.1000A>T (p.Thr334Ser) c.1039A>T (p.Thr347Ser) c.940A>T (p.Thr314Ser) c.889A>T (p.Thr297Ser) | |
| 9 | g.113388995T>C | CA198545533 | ALAD | c.913A>G (p.Thr305Ala) n.1186A>G c.1000A>G (p.Thr334Ala) c.1039A>G (p.Thr347Ala) c.940A>G (p.Thr314Ala) c.889A>G (p.Thr297Ala) | dbSNP |
| 9 | g.113388995T>G | CA374562935 | ALAD | c.913A>C (p.Thr305Pro) n.1186A>C c.1000A>C (p.Thr334Pro) c.1039A>C (p.Thr347Pro) c.940A>C (p.Thr314Pro) c.889A>C (p.Thr297Pro) | |
| 9 | g.113388995T= | CA1873365574 | ALAD | c.913A= (p.Thr305=) n.1186A= c.1000A= (p.Thr334=) c.1039A= (p.Thr347=) c.940A= (p.Thr314=) c.889A= (p.Thr297=) | |
| 9 | g.113388996C>A | CA374562936 | ALAD | c.912G>T (p.Met304Ile) n.1185G>T c.999G>T (p.Met333Ile) c.1038G>T (p.Met346Ile) c.939G>T (p.Met313Ile) c.888G>T (p.Met296Ile) | |
| 9 | g.113388996C>G | CA374562937 | ALAD | c.912G>C (p.Met304Ile) n.1185G>C c.999G>C (p.Met333Ile) c.1038G>C (p.Met346Ile) c.939G>C (p.Met313Ile) c.888G>C (p.Met296Ile) | |
| 9 | g.113388996C>T | CA374562938 | ALAD | c.912G>A (p.Met304Ile) n.1185G>A c.999G>A (p.Met333Ile) c.1038G>A (p.Met346Ile) c.939G>A (p.Met313Ile) c.888G>A (p.Met296Ile) | |
| 9 | g.113388997A= | CA1873365575 | ALAD | c.911T= (p.Met304=) n.1184T= c.998T= (p.Met333=) c.1037T= (p.Met346=) c.938T= (p.Met313=) c.887T= (p.Met296=) | |
| 9 | g.113388997A>C | CA374562939 | ALAD | c.911T>G (p.Met304Arg) n.1184T>G c.998T>G (p.Met333Arg) c.1037T>G (p.Met346Arg) c.938T>G (p.Met313Arg) c.887T>G (p.Met296Arg) | |
| 9 | g.113388997A>G | CA5196317 | ALAD | c.911T>C (p.Met304Thr) n.1184T>C c.998T>C (p.Met333Thr) c.1037T>C (p.Met346Thr) c.938T>C (p.Met313Thr) c.887T>C (p.Met296Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.113388997A>T | CA374562940 | ALAD | c.911T>A (p.Met304Lys) n.1184T>A c.998T>A (p.Met333Lys) c.1037T>A (p.Met346Lys) c.938T>A (p.Met313Lys) c.887T>A (p.Met296Lys) | |
| 9 | g.113388998T>A | CA374562941 | ALAD | c.910A>T (p.Met304Leu) n.1183A>T c.997A>T (p.Met333Leu) c.1036A>T (p.Met346Leu) c.937A>T (p.Met313Leu) c.886A>T (p.Met296Leu) | |
| 9 | g.113388998T>C | CA374562942 | ALAD | c.910A>G (p.Met304Val) n.1183A>G c.997A>G (p.Met333Val) c.1036A>G (p.Met346Val) c.937A>G (p.Met313Val) c.886A>G (p.Met296Val) | ClinVar dbSNP |
| 9 | g.113388998T>G | CA374562943 | ALAD | c.910A>C (p.Met304Leu) n.1183A>C c.997A>C (p.Met333Leu) c.1036A>C (p.Met346Leu) c.937A>C (p.Met313Leu) c.886A>C (p.Met296Leu) | |
| 9 | g.113388998T= | CA1873365576 | ALAD | c.910A= (p.Met304=) n.1183A= c.997A= (p.Met333=) c.1036A= (p.Met346=) c.937A= (p.Met313=) c.886A= (p.Met296=) | |
| 9 | g.113388999G>A | CA5196318 | ALAD | c.909C>T (p.Ala303=) n.1182C>T c.996C>T (p.Ala332=) c.1035C>T (p.Ala345=) c.936C>T (p.Ala312=) c.885C>T (p.Ala295=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.113388999G>C | CA466754897 | ALAD | c.909C>G (p.Ala303=) n.1182C>G c.996C>G (p.Ala332=) c.1035C>G (p.Ala345=) c.936C>G (p.Ala312=) c.885C>G (p.Ala295=) | |
| 9 | g.113388999G= | CA1873365577 | ALAD | c.909C= (p.Ala303=) n.1182C= c.996C= (p.Ala332=) c.1035C= (p.Ala345=) c.936C= (p.Ala312=) c.885C= (p.Ala295=) | |
| 9 | g.113388999G>T | CA466754896 | ALAD | c.909C>A (p.Ala303=) n.1182C>A c.996C>A (p.Ala332=) c.1035C>A (p.Ala345=) c.936C>A (p.Ala312=) c.885C>A (p.Ala295=) | |
| 9 | g.113389000G>A | CA374562944 | ALAD | c.908C>T (p.Ala303Val) n.1181C>T c.995C>T (p.Ala332Val) c.1034C>T (p.Ala345Val) c.935C>T (p.Ala312Val) c.884C>T (p.Ala295Val) | |
| 9 | g.113389000G>C | CA374562945 | ALAD | c.908C>G (p.Ala303Gly) n.1181C>G c.995C>G (p.Ala332Gly) c.1034C>G (p.Ala345Gly) c.935C>G (p.Ala312Gly) c.884C>G (p.Ala295Gly) | |
| 9 | g.113389000G>T | CA374562946 | ALAD | c.908C>A (p.Ala303Asp) n.1181C>A c.995C>A (p.Ala332Asp) c.1034C>A (p.Ala345Asp) c.935C>A (p.Ala312Asp) c.884C>A (p.Ala295Asp) | |
| 9 | g.113389001C>A | CA198545546 | ALAD | c.907G>T (p.Ala303Ser) n.1180G>T c.994G>T (p.Ala332Ser) c.1033G>T (p.Ala345Ser) c.934G>T (p.Ala312Ser) c.883G>T (p.Ala295Ser) | dbSNP |
| 9 | g.113389001C= | CA1873365578 | ALAD | c.907G= (p.Ala303=) n.1180G= c.994G= (p.Ala332=) c.1033G= (p.Ala345=) c.934G= (p.Ala312=) c.883G= (p.Ala295=) | |
| 9 | g.113389001C>G | CA374562947 | ALAD | c.907G>C (p.Ala303Pro) n.1180G>C c.994G>C (p.Ala332Pro) c.1033G>C (p.Ala345Pro) c.934G>C (p.Ala312Pro) c.883G>C (p.Ala295Pro) | |
| 9 | g.113389001C>T | CA374562948 | ALAD | c.907G>A (p.Ala303Thr) n.1180G>A c.994G>A (p.Ala332Thr) c.1033G>A (p.Ala345Thr) c.934G>A (p.Ala312Thr) c.883G>A (p.Ala295Thr) | |
| 9 | g.113389002C>A | CA374562949 | ALAD | c.906G>T (p.Glu302Asp) n.1179G>T c.993G>T (p.Glu331Asp) c.1032G>T (p.Glu344Asp) c.933G>T (p.Glu311Asp) c.882G>T (p.Glu294Asp) |