Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.89935608C>A | CA397476850 | TUBB3 | c.1157C>A (p.Thr386Lys) n.4578C>A c.941C>A (p.Thr314Lys) c.277+2030C>A (n.277+2030C>A) c.*1242C>A (n.*1242C>A) c.2198C>A (p.Thr733Lys) | |
16 | g.89935608C>G | CA397476851 | TUBB3 | c.1157C>G (p.Thr386Arg) n.4578C>G c.941C>G (p.Thr314Arg) c.277+2030C>G (n.277+2030C>G) c.*1242C>G (n.*1242C>G) c.2198C>G (p.Thr733Arg) | |
16 | g.89935608C>T | CA397476852 | TUBB3 | c.1157C>T (p.Thr386Met) n.4578C>T c.941C>T (p.Thr314Met) c.277+2030C>T (n.277+2030C>T) c.*1242C>T (n.*1242C>T) c.2198C>T (p.Thr733Met) | ClinVar dbSNP gnomAD v4 COSMIC |
16 | g.89935609G>A | CA8256215 | TUBB3 | c.1158G>A (p.Thr386=) n.4579G>A c.942G>A (p.Thr314=) c.277+2031G>A (n.277+2031G>A) c.*1243G>A (n.*1243G>A) c.2199G>A (p.Thr733=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935609G>C | CA497381684 | TUBB3 | c.1158G>C (p.Thr386=) n.4579G>C c.942G>C (p.Thr314=) c.277+2031G>C (n.277+2031G>C) c.*1243G>C (n.*1243G>C) c.2199G>C (p.Thr733=) | |
16 | g.89935609G= | CA2242020639 | TUBB3 | c.1158G= (p.Thr386=) n.4579G= c.942G= (p.Thr314=) c.277+2031G= (n.277+2031G=) c.*1243G= (n.*1243G=) c.2199G= (p.Thr733=) | |
16 | g.89935609G>T | CA8256216 | TUBB3 | c.1158G>T (p.Thr386=) n.4579G>T c.942G>T (p.Thr314=) c.277+2031G>T (n.277+2031G>T) c.*1243G>T (n.*1243G>T) c.2199G>T (p.Thr733=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.89935610G>A | CA397476853 | TUBB3 | c.1159G>A (p.Ala387Thr) n.4580G>A c.943G>A (p.Ala315Thr) c.277+2032G>A (n.277+2032G>A) c.*1244G>A (n.*1244G>A) c.2200G>A (p.Ala734Thr) | |
16 | g.89935610G>C | CA397476854 | TUBB3 | c.1159G>C (p.Ala387Pro) n.4580G>C c.943G>C (p.Ala315Pro) c.277+2032G>C (n.277+2032G>C) c.*1244G>C (n.*1244G>C) c.2200G>C (p.Ala734Pro) | |
16 | g.89935610G>T | CA397476855 | TUBB3 | c.1159G>T (p.Ala387Ser) n.4580G>T c.943G>T (p.Ala315Ser) c.277+2032G>T (n.277+2032G>T) c.*1244G>T (n.*1244G>T) c.2200G>T (p.Ala734Ser) | |
16 | g.89935611C>A | CA397476856 | TUBB3 | c.1160C>A (p.Ala387Asp) n.4581C>A c.944C>A (p.Ala315Asp) c.277+2033C>A (n.277+2033C>A) c.*1245C>A (n.*1245C>A) c.2201C>A (p.Ala734Asp) | COSMIC |
16 | g.89935611C>G | CA397476857 | TUBB3 | c.1160C>G (p.Ala387Gly) n.4581C>G c.944C>G (p.Ala315Gly) c.277+2033C>G (n.277+2033C>G) c.*1245C>G (n.*1245C>G) c.2201C>G (p.Ala734Gly) | |
16 | g.89935611C>T | CA397476858 | TUBB3 | c.1160C>T (p.Ala387Val) n.4581C>T c.944C>T (p.Ala315Val) c.277+2033C>T (n.277+2033C>T) c.*1245C>T (n.*1245C>T) c.2201C>T (p.Ala734Val) | |
16 | g.89935612C>A | CA497194413 | TUBB3 | c.1161C>A (p.Ala387=) n.4582C>A c.945C>A (p.Ala315=) c.277+2034C>A (n.277+2034C>A) c.*1246C>A (n.*1246C>A) c.2202C>A (p.Ala734=) | |
16 | g.89935612C>G | CA497194414 | TUBB3 | c.1161C>G (p.Ala387=) n.4582C>G c.945C>G (p.Ala315=) c.277+2034C>G (n.277+2034C>G) c.*1246C>G (n.*1246C>G) c.2202C>G (p.Ala734=) | |
16 | g.89935612C>T | CA497194415 | TUBB3 | c.1161C>T (p.Ala387=) n.4582C>T c.945C>T (p.Ala315=) c.277+2034C>T (n.277+2034C>T) c.*1246C>T (n.*1246C>T) c.2202C>T (p.Ala734=) | |
16 | g.89935613A= | CA2242020645 | TUBB3 | c.1162A= (p.Met388=) n.4583A= c.946A= (p.Met316=) c.277+2035A= (n.277+2035A=) c.*1247A= (n.*1247A=) c.2203A= (p.Met735=) | |
16 | g.89935613A>C | CA397476859 | TUBB3 | c.1162A>C (p.Met388Leu) n.4583A>C c.946A>C (p.Met316Leu) c.277+2035A>C (n.277+2035A>C) c.*1247A>C (n.*1247A>C) c.2203A>C (p.Met735Leu) | |
16 | g.89935613A>G | CA10581578 | TUBB3 | c.1162A>G (p.Met388Val) n.4583A>G c.946A>G (p.Met316Val) c.277+2035A>G (n.277+2035A>G) c.*1247A>G (n.*1247A>G) c.2203A>G (p.Met735Val) | ClinVar dbSNP |
16 | g.89935613A>T | CA397476860 | TUBB3 | c.1162A>T (p.Met388Leu) n.4583A>T c.946A>T (p.Met316Leu) c.277+2035A>T (n.277+2035A>T) c.*1247A>T (n.*1247A>T) c.2203A>T (p.Met735Leu) | |
16 | g.89935614T>A | CA397476861 | TUBB3 | c.1163T>A (p.Met388Lys) n.4584T>A c.947T>A (p.Met316Lys) c.277+2036T>A (n.277+2036T>A) c.*1248T>A (n.*1248T>A) c.2204T>A (p.Met735Lys) | |
16 | g.89935614T>C | CA397476862 | TUBB3 | c.1163T>C (p.Met388Thr) n.4584T>C c.947T>C (p.Met316Thr) c.277+2036T>C (n.277+2036T>C) c.*1248T>C (n.*1248T>C) c.2204T>C (p.Met735Thr) | ClinVar dbSNP |
16 | g.89935614T>G | CA397476863 | TUBB3 | c.1163T>G (p.Met388Arg) n.4584T>G c.947T>G (p.Met316Arg) c.277+2036T>G (n.277+2036T>G) c.*1248T>G (n.*1248T>G) c.2204T>G (p.Met735Arg) | |
16 | g.89935614T= | CA2242020648 | TUBB3 | c.1163T= (p.Met388=) n.4584T= c.947T= (p.Met316=) c.277+2036T= (n.277+2036T=) c.*1248T= (n.*1248T=) c.2204T= (p.Met735=) | |
16 | g.89935615G>A | CA397476866 | TUBB3 | c.1164G>A (p.Met388Ile) n.4585G>A c.948G>A (p.Met316Ile) c.277+2037G>A (n.277+2037G>A) c.*1249G>A (n.*1249G>A) c.2205G>A (p.Met735Ile) | |
16 | g.89935615G>C | CA397476865 | TUBB3 | c.1164G>C (p.Met388Ile) n.4585G>C c.948G>C (p.Met316Ile) c.277+2037G>C (n.277+2037G>C) c.*1249G>C (n.*1249G>C) c.2205G>C (p.Met735Ile) | |
16 | g.89935615G>T | CA397476864 | TUBB3 | c.1164G>T (p.Met388Ile) n.4585G>T c.948G>T (p.Met316Ile) c.277+2037G>T (n.277+2037G>T) c.*1249G>T (n.*1249G>T) c.2205G>T (p.Met735Ile) | |
16 | g.89935616T>A | CA397476869 | TUBB3 | c.1165T>A (p.Phe389Ile) n.4586T>A c.949T>A (p.Phe317Ile) c.277+2038T>A (n.277+2038T>A) c.*1250T>A (n.*1250T>A) c.2206T>A (p.Phe736Ile) | |
16 | g.89935616T>C | CA397476867 | TUBB3 | c.1165T>C (p.Phe389Leu) n.4586T>C c.949T>C (p.Phe317Leu) c.277+2038T>C (n.277+2038T>C) c.*1250T>C (n.*1250T>C) c.2206T>C (p.Phe736Leu) | |
16 | g.89935616T>G | CA397476868 | TUBB3 | c.1165T>G (p.Phe389Val) n.4586T>G c.949T>G (p.Phe317Val) c.277+2038T>G (n.277+2038T>G) c.*1250T>G (n.*1250T>G) c.2206T>G (p.Phe736Val) | ClinVar dbSNP |
16 | g.89935616T= | CA2242020653 | TUBB3 | c.1165T= (p.Phe389=) n.4586T= c.949T= (p.Phe317=) c.277+2038T= (n.277+2038T=) c.*1250T= (n.*1250T=) c.2206T= (p.Phe736=) | |
16 | g.89935617T>A | CA397476870 | TUBB3 | c.1166T>A (p.Phe389Tyr) n.4587T>A c.950T>A (p.Phe317Tyr) c.277+2039T>A (n.277+2039T>A) c.*1251T>A (n.*1251T>A) c.2207T>A (p.Phe736Tyr) | |
16 | g.89935617T>C | CA397476871 | TUBB3 | c.1166T>C (p.Phe389Ser) n.4587T>C c.950T>C (p.Phe317Ser) c.277+2039T>C (n.277+2039T>C) c.*1251T>C (n.*1251T>C) c.2207T>C (p.Phe736Ser) | |
16 | g.89935617T>G | CA397476872 | TUBB3 | c.1166T>G (p.Phe389Cys) n.4587T>G c.950T>G (p.Phe317Cys) c.277+2039T>G (n.277+2039T>G) c.*1251T>G (n.*1251T>G) c.2207T>G (p.Phe736Cys) | |
16 | g.89935618C>A | CA397476873 | TUBB3 | c.1167C>A (p.Phe389Leu) n.4588C>A c.951C>A (p.Phe317Leu) c.277+2040C>A (n.277+2040C>A) c.*1252C>A (n.*1252C>A) c.2208C>A (p.Phe736Leu) | |
16 | g.89935618C= | CA2242020658 | TUBB3 | c.1167C= (p.Phe389=) n.4588C= c.951C= (p.Phe317=) c.277+2040C= (n.277+2040C=) c.*1252C= (n.*1252C=) c.2208C= (p.Phe736=) | |
16 | g.89935618C>G | CA397476874 | TUBB3 | c.1167C>G (p.Phe389Leu) n.4588C>G c.951C>G (p.Phe317Leu) c.277+2040C>G (n.277+2040C>G) c.*1252C>G (n.*1252C>G) c.2208C>G (p.Phe736Leu) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.89935618C>T | CA497194416 | TUBB3 | c.1167C>T (p.Phe389=) n.4588C>T c.951C>T (p.Phe317=) c.277+2040C>T (n.277+2040C>T) c.*1252C>T (n.*1252C>T) c.2208C>T (p.Phe736=) | gnomAD v4 |
16 | g.89935619C>A | CA497194417 | TUBB3 | c.1168C>A (p.Arg390=) n.4589C>A c.952C>A (p.Arg318=) c.277+2041C>A (n.277+2041C>A) c.*1253C>A (n.*1253C>A) c.2209C>A (p.Arg737=) | |
16 | g.89935619C>G | CA397476875 | TUBB3 | c.1168C>G (p.Arg390Gly) n.4589C>G c.952C>G (p.Arg318Gly) c.277+2041C>G (n.277+2041C>G) c.*1253C>G (n.*1253C>G) c.2209C>G (p.Arg737Gly) | |
16 | g.89935619C>T | CA397476876 | TUBB3 | c.1168C>T (p.Arg390Trp) n.4589C>T c.952C>T (p.Arg318Trp) c.277+2041C>T (n.277+2041C>T) c.*1253C>T (n.*1253C>T) c.2209C>T (p.Arg737Trp) | |
16 | g.89935620G>A | CA397476877 | TUBB3 | c.1169G>A (p.Arg390Gln) n.4590G>A c.953G>A (p.Arg318Gln) c.277+2042G>A (n.277+2042G>A) c.*1254G>A (n.*1254G>A) c.2210G>A (p.Arg737Gln) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
16 | g.89935620G>C | CA10604051 | TUBB3 | c.1169G>C (p.Arg390Pro) n.4590G>C c.953G>C (p.Arg318Pro) c.277+2042G>C (n.277+2042G>C) c.*1254G>C (n.*1254G>C) c.2210G>C (p.Arg737Pro) | ClinVar dbSNP |
16 | g.89935620G= | CA2242020662 | TUBB3 | c.1169G= (p.Arg390=) n.4590G= c.953G= (p.Arg318=) c.277+2042G= (n.277+2042G=) c.*1254G= (n.*1254G=) c.2210G= (p.Arg737=) | |
16 | g.89935620G>T | CA397476878 | TUBB3 | c.1169G>T (p.Arg390Leu) n.4590G>T c.953G>T (p.Arg318Leu) c.277+2042G>T (n.277+2042G>T) c.*1254G>T (n.*1254G>T) c.2210G>T (p.Arg737Leu) | |
16 | g.89935621G>A | CA213291 | TUBB3 | c.1170G>A (p.Arg390=) n.4591G>A c.954G>A (p.Arg318=) c.277+2043G>A (n.277+2043G>A) c.*1255G>A (n.*1255G>A) c.2211G>A (p.Arg737=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935621G>C | CA497194419 | TUBB3 | c.1170G>C (p.Arg390=) n.4591G>C c.954G>C (p.Arg318=) c.277+2043G>C (n.277+2043G>C) c.*1255G>C (n.*1255G>C) c.2211G>C (p.Arg737=) | |
16 | g.89935621G= | CA2242020666 | TUBB3 | c.1170G= (p.Arg390=) n.4591G= c.954G= (p.Arg318=) c.277+2043G= (n.277+2043G=) c.*1255G= (n.*1255G=) c.2211G= (p.Arg737=) | |
16 | g.89935621G>T | CA497194418 | TUBB3 | c.1170G>T (p.Arg390=) n.4591G>T c.954G>T (p.Arg318=) c.277+2043G>T (n.277+2043G>T) c.*1255G>T (n.*1255G>T) c.2211G>T (p.Arg737=) | |
16 | g.89935622C>A | CA397476881 | TUBB3 | c.1171C>A (p.Arg391Ser) n.4592C>A c.955C>A (p.Arg319Ser) c.277+2044C>A (n.277+2044C>A) c.*1256C>A (n.*1256C>A) c.2212C>A (p.Arg738Ser) | |
16 | g.89935622C= | CA2242020671 | TUBB3 | c.1171C= (p.Arg391=) n.4592C= c.955C= (p.Arg319=) c.277+2044C= (n.277+2044C=) c.*1256C= (n.*1256C=) c.2212C= (p.Arg738=) | |
16 | g.89935622C>G | CA397476880 | TUBB3 | c.1171C>G (p.Arg391Gly) n.4592C>G c.955C>G (p.Arg319Gly) c.277+2044C>G (n.277+2044C>G) c.*1256C>G (n.*1256C>G) c.2212C>G (p.Arg738Gly) | |
16 | g.89935622C>T | CA397476879 | TUBB3 | c.1171C>T (p.Arg391Cys) n.4592C>T c.955C>T (p.Arg319Cys) c.277+2044C>T (n.277+2044C>T) c.*1256C>T (n.*1256C>T) c.2212C>T (p.Arg738Cys) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.89935623G>A | CA397476882 | TUBB3 | c.1172G>A (p.Arg391His) n.4593G>A c.956G>A (p.Arg319His) c.277+2045G>A (n.277+2045G>A) c.*1257G>A (n.*1257G>A) c.2213G>A (p.Arg738His) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
16 | g.89935623G>C | CA397476883 | TUBB3 | c.1172G>C (p.Arg391Pro) n.4593G>C c.956G>C (p.Arg319Pro) c.277+2045G>C (n.277+2045G>C) c.*1257G>C (n.*1257G>C) c.2213G>C (p.Arg738Pro) | gnomAD v4 |
16 | g.89935623G= | CA2242020683 | TUBB3 | c.1172G= (p.Arg391=) n.4593G= c.956G= (p.Arg319=) c.277+2045G= (n.277+2045G=) c.*1257G= (n.*1257G=) c.2213G= (p.Arg738=) | |
16 | g.89935623G>T | CA10588636 | TUBB3 | c.1172G>T (p.Arg391Leu) n.4593G>T c.956G>T (p.Arg319Leu) c.277+2045G>T (n.277+2045G>T) c.*1257G>T (n.*1257G>T) c.2213G>T (p.Arg738Leu) | ClinVar dbSNP |
16 | g.89935624C>A | CA497194420 | TUBB3 | c.1173C>A (p.Arg391=) n.4594C>A c.957C>A (p.Arg319=) c.277+2046C>A (n.277+2046C>A) c.*1258C>A (n.*1258C>A) c.2214C>A (p.Arg738=) | |
16 | g.89935624C= | CA2242020687 | TUBB3 | c.1173C= (p.Arg391=) n.4594C= c.957C= (p.Arg319=) c.277+2046C= (n.277+2046C=) c.*1258C= (n.*1258C=) c.2214C= (p.Arg738=) | |
16 | g.89935624C>G | CA497194421 | TUBB3 | c.1173C>G (p.Arg391=) n.4594C>G c.957C>G (p.Arg319=) c.277+2046C>G (n.277+2046C>G) c.*1258C>G (n.*1258C>G) c.2214C>G (p.Arg738=) | dbSNP |
16 | g.89935624C>T | CA497194422 | TUBB3 | c.1173C>T (p.Arg391=) n.4594C>T c.957C>T (p.Arg319=) c.277+2046C>T (n.277+2046C>T) c.*1258C>T (n.*1258C>T) c.2214C>T (p.Arg738=) | |
16 | g.89935625A>C | CA397476884 | TUBB3 | c.1174A>C (p.Lys392Gln) n.4595A>C c.958A>C (p.Lys320Gln) c.277+2047A>C (n.277+2047A>C) c.*1259A>C (n.*1259A>C) c.2215A>C (p.Lys739Gln) | gnomAD v4 |
16 | g.89935625A>G | CA397476885 | TUBB3 | c.1174A>G (p.Lys392Glu) n.4595A>G c.958A>G (p.Lys320Glu) c.277+2047A>G (n.277+2047A>G) c.*1259A>G (n.*1259A>G) c.2215A>G (p.Lys739Glu) | |
16 | g.89935625A>T | CA397476886 | TUBB3 | c.1174A>T (p.Lys392Ter) n.4595A>T c.958A>T (p.Lys320Ter) c.277+2047A>T (n.277+2047A>T) c.*1259A>T (n.*1259A>T) c.2215A>T (p.Lys739Ter) | |
16 | g.89935626A>C | CA397476887 | TUBB3 | c.1175A>C (p.Lys392Thr) n.4596A>C c.959A>C (p.Lys320Thr) c.277+2048A>C (n.277+2048A>C) c.*1260A>C (n.*1260A>C) c.2216A>C (p.Lys739Thr) | |
16 | g.89935626A>G | CA397476888 | TUBB3 | c.1175A>G (p.Lys392Arg) n.4596A>G c.959A>G (p.Lys320Arg) c.277+2048A>G (n.277+2048A>G) c.*1260A>G (n.*1260A>G) c.2216A>G (p.Lys739Arg) | |
16 | g.89935626A>T | CA397476889 | TUBB3 | c.1175A>T (p.Lys392Met) n.4596A>T c.959A>T (p.Lys320Met) c.277+2048A>T (n.277+2048A>T) c.*1260A>T (n.*1260A>T) c.2216A>T (p.Lys739Met) | |
16 | g.89935627G>A | CA497194423 | TUBB3 | c.1176G>A (p.Lys392=) n.4597G>A c.960G>A (p.Lys320=) c.277+2049G>A (n.277+2049G>A) c.*1261G>A (n.*1261G>A) c.2217G>A (p.Lys739=) | |
16 | g.89935627G>C | CA397476890 | TUBB3 | c.1176G>C (p.Lys392Asn) n.4597G>C c.960G>C (p.Lys320Asn) c.277+2049G>C (n.277+2049G>C) c.*1261G>C (n.*1261G>C) c.2217G>C (p.Lys739Asn) | |
16 | g.89935627G>T | CA397476891 | TUBB3 | c.1176G>T (p.Lys392Asn) n.4597G>T c.960G>T (p.Lys320Asn) c.277+2049G>T (n.277+2049G>T) c.*1261G>T (n.*1261G>T) c.2217G>T (p.Lys739Asn) | |
16 | g.89935628G>A | CA397476892 | TUBB3 | c.1177G>A (p.Ala393Thr) n.4598G>A c.961G>A (p.Ala321Thr) c.277+2050G>A (n.277+2050G>A) c.*1262G>A (n.*1262G>A) c.2218G>A (p.Ala740Thr) | |
16 | g.89935628G>C | CA397476893 | TUBB3 | c.1177G>C (p.Ala393Pro) n.4598G>C c.961G>C (p.Ala321Pro) c.277+2050G>C (n.277+2050G>C) c.*1262G>C (n.*1262G>C) c.2218G>C (p.Ala740Pro) | |
16 | g.89935628G>T | CA397476894 | TUBB3 | c.1177G>T (p.Ala393Ser) n.4598G>T c.961G>T (p.Ala321Ser) c.277+2050G>T (n.277+2050G>T) c.*1262G>T (n.*1262G>T) c.2218G>T (p.Ala740Ser) | |
16 | g.89935629C>A | CA397476896 | TUBB3 | c.1178C>A (p.Ala393Asp) n.4599C>A c.962C>A (p.Ala321Asp) c.277+2051C>A (n.277+2051C>A) c.*1263C>A (n.*1263C>A) c.2219C>A (p.Ala740Asp) | |
16 | g.89935629C>G | CA397476897 | TUBB3 | c.1178C>G (p.Ala393Gly) n.4599C>G c.962C>G (p.Ala321Gly) c.277+2051C>G (n.277+2051C>G) c.*1263C>G (n.*1263C>G) c.2219C>G (p.Ala740Gly) | |
16 | g.89935629C>T | CA397476895 | TUBB3 | c.1178C>T (p.Ala393Val) n.4599C>T c.962C>T (p.Ala321Val) c.277+2051C>T (n.277+2051C>T) c.*1263C>T (n.*1263C>T) c.2219C>T (p.Ala740Val) | |
16 | g.89935630C>A | CA497194424 | TUBB3 | c.1179C>A (p.Ala393=) n.4600C>A c.963C>A (p.Ala321=) c.277+2052C>A (n.277+2052C>A) c.*1264C>A (n.*1264C>A) c.2220C>A (p.Ala740=) | |
16 | g.89935630C>G | CA497194425 | TUBB3 | c.1179C>G (p.Ala393=) n.4600C>G c.963C>G (p.Ala321=) c.277+2052C>G (n.277+2052C>G) c.*1264C>G (n.*1264C>G) c.2220C>G (p.Ala740=) | |
16 | g.89935630C>T | CA497194426 | TUBB3 | c.1179C>T (p.Ala393=) n.4600C>T c.963C>T (p.Ala321=) c.277+2052C>T (n.277+2052C>T) c.*1264C>T (n.*1264C>T) c.2220C>T (p.Ala740=) | gnomAD v4 |
16 | g.89935631T>A | CA397476898 | TUBB3 | c.1180T>A (p.Phe394Ile) n.4601T>A c.964T>A (p.Phe322Ile) c.277+2053T>A (n.277+2053T>A) c.*1265T>A (n.*1265T>A) c.2221T>A (p.Phe741Ile) | |
16 | g.89935631T>C | CA397476899 | TUBB3 | c.1180T>C (p.Phe394Leu) n.4601T>C c.964T>C (p.Phe322Leu) c.277+2053T>C (n.277+2053T>C) c.*1265T>C (n.*1265T>C) c.2221T>C (p.Phe741Leu) | |
16 | g.89935631T>G | CA397476900 | TUBB3 | c.1180T>G (p.Phe394Val) n.4601T>G c.964T>G (p.Phe322Val) c.277+2053T>G (n.277+2053T>G) c.*1265T>G (n.*1265T>G) c.2221T>G (p.Phe741Val) | |
16 | g.89935632T>A | CA397476901 | TUBB3 | c.1181T>A (p.Phe394Tyr) n.4602T>A c.965T>A (p.Phe322Tyr) c.277+2054T>A (n.277+2054T>A) c.*1266T>A (n.*1266T>A) c.2222T>A (p.Phe741Tyr) | |
16 | g.89935632T>C | CA397476902 | TUBB3 | c.1181T>C (p.Phe394Ser) n.4602T>C c.965T>C (p.Phe322Ser) c.277+2054T>C (n.277+2054T>C) c.*1266T>C (n.*1266T>C) c.2222T>C (p.Phe741Ser) | |
16 | g.89935632T>G | CA397476903 | TUBB3 | c.1181T>G (p.Phe394Cys) n.4602T>G c.965T>G (p.Phe322Cys) c.277+2054T>G (n.277+2054T>G) c.*1266T>G (n.*1266T>G) c.2222T>G (p.Phe741Cys) | |
16 | g.89935633C>A | CA397476905 | TUBB3 | c.1182C>A (p.Phe394Leu) n.4603C>A c.966C>A (p.Phe322Leu) c.277+2055C>A (n.277+2055C>A) c.*1267C>A (n.*1267C>A) c.2223C>A (p.Phe741Leu) | |
16 | g.89935633C>G | CA397476904 | TUBB3 | c.1182C>G (p.Phe394Leu) n.4603C>G c.966C>G (p.Phe322Leu) c.277+2055C>G (n.277+2055C>G) c.*1267C>G (n.*1267C>G) c.2223C>G (p.Phe741Leu) | |
16 | g.89935633C>T | CA497194427 | TUBB3 | c.1182C>T (p.Phe394=) n.4603C>T c.966C>T (p.Phe322=) c.277+2055C>T (n.277+2055C>T) c.*1267C>T (n.*1267C>T) c.2223C>T (p.Phe741=) | gnomAD v4 |
16 | g.89935634C>A | CA397476906 | TUBB3 | c.1183C>A (p.Leu395Met) n.4604C>A c.967C>A (p.Leu323Met) c.277+2056C>A (n.277+2056C>A) c.*1268C>A (n.*1268C>A) c.2224C>A (p.Leu742Met) | |
16 | g.89935634C= | CA2242020689 | TUBB3 | c.1183C= (p.Leu395=) n.4604C= c.967C= (p.Leu323=) c.277+2056C= (n.277+2056C=) c.*1268C= (n.*1268C=) c.2224C= (p.Leu742=) | |
16 | g.89935634C>G | CA397476907 | TUBB3 | c.1183C>G (p.Leu395Val) n.4604C>G c.967C>G (p.Leu323Val) c.277+2056C>G (n.277+2056C>G) c.*1268C>G (n.*1268C>G) c.2224C>G (p.Leu742Val) | |
16 | g.89935634C>T | CA8256217 | TUBB3 | c.1183C>T (p.Leu395=) n.4604C>T c.967C>T (p.Leu323=) c.277+2056C>T (n.277+2056C>T) c.*1268C>T (n.*1268C>T) c.2224C>T (p.Leu742=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935635T>A | CA397476908 | TUBB3 | c.1184T>A (p.Leu395Gln) n.4605T>A c.968T>A (p.Leu323Gln) c.277+2057T>A (n.277+2057T>A) c.*1269T>A (n.*1269T>A) c.2225T>A (p.Leu742Gln) | |
16 | g.89935635T>C | CA397476909 | TUBB3 | c.1184T>C (p.Leu395Pro) n.4605T>C c.968T>C (p.Leu323Pro) c.277+2057T>C (n.277+2057T>C) c.*1269T>C (n.*1269T>C) c.2225T>C (p.Leu742Pro) | |
16 | g.89935635T>G | CA397476910 | TUBB3 | c.1184T>G (p.Leu395Arg) n.4605T>G c.968T>G (p.Leu323Arg) c.277+2057T>G (n.277+2057T>G) c.*1269T>G (n.*1269T>G) c.2225T>G (p.Leu742Arg) | |
16 | g.89935636G>A | CA497194428 | TUBB3 | c.1185G>A (p.Leu395=) n.4606G>A c.969G>A (p.Leu323=) c.277+2058G>A (n.277+2058G>A) c.*1270G>A (n.*1270G>A) c.2226G>A (p.Leu742=) | |
16 | g.89935636G>C | CA497194429 | TUBB3 | c.1185G>C (p.Leu395=) n.4606G>C c.969G>C (p.Leu323=) c.277+2058G>C (n.277+2058G>C) c.*1270G>C (n.*1270G>C) c.2226G>C (p.Leu742=) | |
16 | g.89935636G>T | CA497194430 | TUBB3 | c.1185G>T (p.Leu395=) n.4606G>T c.969G>T (p.Leu323=) c.277+2058G>T (n.277+2058G>T) c.*1270G>T (n.*1270G>T) c.2226G>T (p.Leu742=) | gnomAD v4 |
16 | g.89935637C>A | CA397476911 | TUBB3 | c.1186C>A (p.His396Asn) n.4607C>A c.970C>A (p.His324Asn) c.277+2059C>A (n.277+2059C>A) c.*1271C>A (n.*1271C>A) c.2227C>A (p.His743Asn) | |
16 | g.89935637C>G | CA397476913 | TUBB3 | c.1186C>G (p.His396Asp) n.4607C>G c.970C>G (p.His324Asp) c.277+2059C>G (n.277+2059C>G) c.*1271C>G (n.*1271C>G) c.2227C>G (p.His743Asp) | |
16 | g.89935637C>T | CA397476912 | TUBB3 | c.1186C>T (p.His396Tyr) n.4607C>T c.970C>T (p.His324Tyr) c.277+2059C>T (n.277+2059C>T) c.*1271C>T (n.*1271C>T) c.2227C>T (p.His743Tyr) | |
16 | g.89935638A>C | CA397476914 | TUBB3 | c.1187A>C (p.His396Pro) n.4608A>C c.971A>C (p.His324Pro) c.277+2060A>C (n.277+2060A>C) c.*1272A>C (n.*1272A>C) c.2228A>C (p.His743Pro) | |
16 | g.89935638A>G | CA397476915 | TUBB3 | c.1187A>G (p.His396Arg) n.4608A>G c.971A>G (p.His324Arg) c.277+2060A>G (n.277+2060A>G) c.*1272A>G (n.*1272A>G) c.2228A>G (p.His743Arg) | |
16 | g.89935638A>T | CA397476916 | TUBB3 | c.1187A>T (p.His396Leu) n.4608A>T c.971A>T (p.His324Leu) c.277+2060A>T (n.277+2060A>T) c.*1272A>T (n.*1272A>T) c.2228A>T (p.His743Leu) | |
16 | g.89935639C>A | CA397476917 | TUBB3 | c.1188C>A (p.His396Gln) n.4609C>A c.972C>A (p.His324Gln) c.277+2061C>A (n.277+2061C>A) c.*1273C>A (n.*1273C>A) c.2229C>A (p.His743Gln) | |
16 | g.89935639C>G | CA397476918 | TUBB3 | c.1188C>G (p.His396Gln) n.4609C>G c.972C>G (p.His324Gln) c.277+2061C>G (n.277+2061C>G) c.*1273C>G (n.*1273C>G) c.2229C>G (p.His743Gln) | ClinVar |
16 | g.89935639C>T | CA497194431 | TUBB3 | c.1188C>T (p.His396=) n.4609C>T c.972C>T (p.His324=) c.277+2061C>T (n.277+2061C>T) c.*1273C>T (n.*1273C>T) c.2229C>T (p.His743=) | |
16 | g.89935640T>A | CA397476919 | TUBB3 | c.1189T>A (p.Trp397Arg) n.4610T>A c.973T>A (p.Trp325Arg) c.277+2062T>A (n.277+2062T>A) c.*1274T>A (n.*1274T>A) c.2230T>A (p.Trp744Arg) | |
16 | g.89935640T>C | CA397476920 | TUBB3 | c.1189T>C (p.Trp397Arg) n.4610T>C c.973T>C (p.Trp325Arg) c.277+2062T>C (n.277+2062T>C) c.*1274T>C (n.*1274T>C) c.2230T>C (p.Trp744Arg) | |
16 | g.89935640T>G | CA397476921 | TUBB3 | c.1189T>G (p.Trp397Gly) n.4610T>G c.973T>G (p.Trp325Gly) c.277+2062T>G (n.277+2062T>G) c.*1274T>G (n.*1274T>G) c.2230T>G (p.Trp744Gly) | |
16 | g.89935641G>A | CA397476922 | TUBB3 | c.1190G>A (p.Trp397Ter) n.4611G>A c.974G>A (p.Trp325Ter) c.277+2063G>A (n.277+2063G>A) c.*1275G>A (n.*1275G>A) c.2231G>A (p.Trp744Ter) | |
16 | g.89935641G>C | CA397476923 | TUBB3 | c.1190G>C (p.Trp397Ser) n.4611G>C c.974G>C (p.Trp325Ser) c.277+2063G>C (n.277+2063G>C) c.*1275G>C (n.*1275G>C) c.2231G>C (p.Trp744Ser) | |
16 | g.89935641G>T | CA397476924 | TUBB3 | c.1190G>T (p.Trp397Leu) n.4611G>T c.974G>T (p.Trp325Leu) c.277+2063G>T (n.277+2063G>T) c.*1275G>T (n.*1275G>T) c.2231G>T (p.Trp744Leu) | |
16 | g.89935642G>A | CA397476926 | TUBB3 | c.1191G>A (p.Trp397Ter) n.4612G>A c.975G>A (p.Trp325Ter) c.277+2064G>A (n.277+2064G>A) c.*1276G>A (n.*1276G>A) c.2232G>A (p.Trp744Ter) | |
16 | g.89935642G>C | CA397476927 | TUBB3 | c.1191G>C (p.Trp397Cys) n.4612G>C c.975G>C (p.Trp325Cys) c.277+2064G>C (n.277+2064G>C) c.*1276G>C (n.*1276G>C) c.2232G>C (p.Trp744Cys) | |
16 | g.89935642G>T | CA397476925 | TUBB3 | c.1191G>T (p.Trp397Cys) n.4612G>T c.975G>T (p.Trp325Cys) c.277+2064G>T (n.277+2064G>T) c.*1276G>T (n.*1276G>T) c.2232G>T (p.Trp744Cys) | |
16 | g.89935643T>A | CA397476928 | TUBB3 | c.1192T>A (p.Tyr398Asn) n.4613T>A c.976T>A (p.Tyr326Asn) c.277+2065T>A (n.277+2065T>A) c.*1277T>A (n.*1277T>A) c.2233T>A (p.Tyr745Asn) | |
16 | g.89935643T>C | CA397476929 | TUBB3 | c.1192T>C (p.Tyr398His) n.4613T>C c.976T>C (p.Tyr326His) c.277+2065T>C (n.277+2065T>C) c.*1277T>C (n.*1277T>C) c.2233T>C (p.Tyr745His) | |
16 | g.89935643T>G | CA397476930 | TUBB3 | c.1192T>G (p.Tyr398Asp) n.4613T>G c.976T>G (p.Tyr326Asp) c.277+2065T>G (n.277+2065T>G) c.*1277T>G (n.*1277T>G) c.2233T>G (p.Tyr745Asp) | |
16 | g.89935644A>C | CA397476931 | TUBB3 | c.1193A>C (p.Tyr398Ser) n.4614A>C c.977A>C (p.Tyr326Ser) c.277+2066A>C (n.277+2066A>C) c.*1278A>C (n.*1278A>C) c.2234A>C (p.Tyr745Ser) | |
16 | g.89935644A>G | CA397476932 | TUBB3 | c.1193A>G (p.Tyr398Cys) n.4614A>G c.977A>G (p.Tyr326Cys) c.277+2066A>G (n.277+2066A>G) c.*1278A>G (n.*1278A>G) c.2234A>G (p.Tyr745Cys) | |
16 | g.89935644A>T | CA397476933 | TUBB3 | c.1193A>T (p.Tyr398Phe) n.4614A>T c.977A>T (p.Tyr326Phe) c.277+2066A>T (n.277+2066A>T) c.*1278A>T (n.*1278A>T) c.2234A>T (p.Tyr745Phe) | |
16 | g.89935645C>A | CA397476934 | TUBB3 | c.1194C>A (p.Tyr398Ter) n.4615C>A c.978C>A (p.Tyr326Ter) c.277+2067C>A (n.277+2067C>A) c.*1279C>A (n.*1279C>A) c.2235C>A (p.Tyr745Ter) | |
16 | g.89935645C>G | CA397476935 | TUBB3 | c.1194C>G (p.Tyr398Ter) n.4615C>G c.978C>G (p.Tyr326Ter) c.277+2067C>G (n.277+2067C>G) c.*1279C>G (n.*1279C>G) c.2235C>G (p.Tyr745Ter) | |
16 | g.89935645C>T | CA497194432 | TUBB3 | c.1194C>T (p.Tyr398=) n.4615C>T c.978C>T (p.Tyr326=) c.277+2067C>T (n.277+2067C>T) c.*1279C>T (n.*1279C>T) c.2235C>T (p.Tyr745=) | |
16 | g.89935646A= | CA2242020692 | TUBB3 | c.1195A= (p.Thr399=) n.4616A= c.979A= (p.Thr327=) c.277+2068A= (n.277+2068A=) c.*1280A= (n.*1280A=) c.2236A= (p.Thr746=) | |
16 | g.89935646A>C | CA397476936 | TUBB3 | c.1195A>C (p.Thr399Pro) n.4616A>C c.979A>C (p.Thr327Pro) c.277+2068A>C (n.277+2068A>C) c.*1280A>C (n.*1280A>C) c.2236A>C (p.Thr746Pro) | |
16 | g.89935646A>G | CA397476938 | TUBB3 | c.1195A>G (p.Thr399Ala) n.4616A>G c.979A>G (p.Thr327Ala) c.277+2068A>G (n.277+2068A>G) c.*1280A>G (n.*1280A>G) c.2236A>G (p.Thr746Ala) | |
16 | g.89935646A>T | CA397476937 | TUBB3 | c.1195A>T (p.Thr399Ser) n.4616A>T c.979A>T (p.Thr327Ser) c.277+2068A>T (n.277+2068A>T) c.*1280A>T (n.*1280A>T) c.2236A>T (p.Thr746Ser) | ClinVar dbSNP |
16 | g.89935647C>A | CA397476939 | TUBB3 | c.1196C>A (p.Thr399Lys) n.4617C>A c.980C>A (p.Thr327Lys) c.277+2069C>A (n.277+2069C>A) c.*1281C>A (n.*1281C>A) c.2237C>A (p.Thr746Lys) | |
16 | g.89935647C= | CA2242020696 | TUBB3 | c.1196C= (p.Thr399=) n.4617C= c.980C= (p.Thr327=) c.277+2069C= (n.277+2069C=) c.*1281C= (n.*1281C=) c.2237C= (p.Thr746=) | |
16 | g.89935647C>G | CA397476940 | TUBB3 | c.1196C>G (p.Thr399Arg) n.4617C>G c.980C>G (p.Thr327Arg) c.277+2069C>G (n.277+2069C>G) c.*1281C>G (n.*1281C>G) c.2237C>G (p.Thr746Arg) | dbSNP |
16 | g.89935647C>T | CA286619350 | TUBB3 | c.1196C>T (p.Thr399Met) n.4617C>T c.980C>T (p.Thr327Met) c.277+2069C>T (n.277+2069C>T) c.*1281C>T (n.*1281C>T) c.2237C>T (p.Thr746Met) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935648G>A | CA8256218 | TUBB3 | c.1197G>A (p.Thr399=) n.4618G>A c.981G>A (p.Thr327=) c.277+2070G>A (n.277+2070G>A) c.*1282G>A (n.*1282G>A) c.2238G>A (p.Thr746=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935648G>C | CA8256219 | TUBB3 | c.1197G>C (p.Thr399=) n.4618G>C c.981G>C (p.Thr327=) c.277+2070G>C (n.277+2070G>C) c.*1282G>C (n.*1282G>C) c.2238G>C (p.Thr746=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.89935648G= | CA2242020700 | TUBB3 | c.1197G= (p.Thr399=) n.4618G= c.981G= (p.Thr327=) c.277+2070G= (n.277+2070G=) c.*1282G= (n.*1282G=) c.2238G= (p.Thr746=) | |
16 | g.89935648G>T | CA497194433 | TUBB3 | c.1197G>T (p.Thr399=) n.4618G>T c.981G>T (p.Thr327=) c.277+2070G>T (n.277+2070G>T) c.*1282G>T (n.*1282G>T) c.2238G>T (p.Thr746=) | |
16 | g.89935649G>A | CA397476941 | TUBB3 | c.1198G>A (p.Gly400Ser) n.4619G>A c.982G>A (p.Gly328Ser) c.277+2071G>A (n.277+2071G>A) c.*1283G>A (n.*1283G>A) c.2239G>A (p.Gly747Ser) | gnomAD v4 |
16 | g.89935649G>C | CA397476943 | TUBB3 | c.1198G>C (p.Gly400Arg) n.4619G>C c.982G>C (p.Gly328Arg) c.277+2071G>C (n.277+2071G>C) c.*1283G>C (n.*1283G>C) c.2239G>C (p.Gly747Arg) | |
16 | g.89935649G>T | CA397476942 | TUBB3 | c.1198G>T (p.Gly400Cys) n.4619G>T c.982G>T (p.Gly328Cys) c.277+2071G>T (n.277+2071G>T) c.*1283G>T (n.*1283G>T) c.2239G>T (p.Gly747Cys) | |
16 | g.89935650G>A | CA397476944 | TUBB3 | c.1199G>A (p.Gly400Asp) n.4620G>A c.983G>A (p.Gly328Asp) c.277+2072G>A (n.277+2072G>A) c.*1284G>A (n.*1284G>A) c.2240G>A (p.Gly747Asp) | |
16 | g.89935650G>C | CA397476945 | TUBB3 | c.1199G>C (p.Gly400Ala) n.4620G>C c.983G>C (p.Gly328Ala) c.277+2072G>C (n.277+2072G>C) c.*1284G>C (n.*1284G>C) c.2240G>C (p.Gly747Ala) | |
16 | g.89935650G>T | CA397476946 | TUBB3 | c.1199G>T (p.Gly400Val) n.4620G>T c.983G>T (p.Gly328Val) c.277+2072G>T (n.277+2072G>T) c.*1284G>T (n.*1284G>T) c.2240G>T (p.Gly747Val) | |
16 | g.89935651C>A | CA497194434 | TUBB3 | c.1200C>A (p.Gly400=) n.4621C>A c.984C>A (p.Gly328=) c.277+2073C>A (n.277+2073C>A) c.*1285C>A (n.*1285C>A) c.2241C>A (p.Gly747=) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.89935651C= | CA2242020706 | TUBB3 | c.1200C= (p.Gly400=) n.4621C= c.984C= (p.Gly328=) c.277+2073C= (n.277+2073C=) c.*1285C= (n.*1285C=) c.2241C= (p.Gly747=) | |
16 | g.89935651C>G | CA497194435 | TUBB3 | c.1200C>G (p.Gly400=) n.4621C>G c.984C>G (p.Gly328=) c.277+2073C>G (n.277+2073C>G) c.*1285C>G (n.*1285C>G) c.2241C>G (p.Gly747=) | |
16 | g.89935651C>T | CA8256220 | TUBB3 | c.1200C>T (p.Gly400=) n.4621C>T c.984C>T (p.Gly328=) c.277+2073C>T (n.277+2073C>T) c.*1285C>T (n.*1285C>T) c.2241C>T (p.Gly747=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935652G>A | CA397476947 | TUBB3 | c.1201G>A (p.Glu401Lys) n.4622G>A c.985G>A (p.Glu329Lys) c.277+2074G>A (n.277+2074G>A) c.*1286G>A (n.*1286G>A) c.2242G>A (p.Glu748Lys) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
16 | g.89935652G>C | CA397476948 | TUBB3 | c.1201G>C (p.Glu401Gln) n.4622G>C c.985G>C (p.Glu329Gln) c.277+2074G>C (n.277+2074G>C) c.*1286G>C (n.*1286G>C) c.2242G>C (p.Glu748Gln) | |
16 | g.89935652G= | CA2242020712 | TUBB3 | c.1201G= (p.Glu401=) n.4622G= c.985G= (p.Glu329=) c.277+2074G= (n.277+2074G=) c.*1286G= (n.*1286G=) c.2242G= (p.Glu748=) | |
16 | g.89935652G>T | CA397476949 | TUBB3 | c.1201G>T (p.Glu401Ter) n.4622G>T c.985G>T (p.Glu329Ter) c.277+2074G>T (n.277+2074G>T) c.*1286G>T (n.*1286G>T) c.2242G>T (p.Glu748Ter) | |
16 | g.89935653A>C | CA397476950 | TUBB3 | c.1202A>C (p.Glu401Ala) n.4623A>C c.986A>C (p.Glu329Ala) c.277+2075A>C (n.277+2075A>C) c.*1287A>C (n.*1287A>C) c.2243A>C (p.Glu748Ala) | |
16 | g.89935653A>G | CA397476951 | TUBB3 | c.1202A>G (p.Glu401Gly) n.4623A>G c.986A>G (p.Glu329Gly) c.277+2075A>G (n.277+2075A>G) c.*1287A>G (n.*1287A>G) c.2243A>G (p.Glu748Gly) | |
16 | g.89935653A>T | CA397476952 | TUBB3 | c.1202A>T (p.Glu401Val) n.4623A>T c.986A>T (p.Glu329Val) c.277+2075A>T (n.277+2075A>T) c.*1287A>T (n.*1287A>T) c.2243A>T (p.Glu748Val) | |
16 | g.89935654G>A | CA497194436 | TUBB3 | c.1203G>A (p.Glu401=) n.4624G>A c.987G>A (p.Glu329=) c.277+2076G>A (n.277+2076G>A) c.*1288G>A (n.*1288G>A) c.2244G>A (p.Glu748=) | dbSNP |
16 | g.89935654G>C | CA397476953 | TUBB3 | c.1203G>C (p.Glu401Asp) n.4624G>C c.987G>C (p.Glu329Asp) c.277+2076G>C (n.277+2076G>C) c.*1288G>C (n.*1288G>C) c.2244G>C (p.Glu748Asp) | |
16 | g.89935654G= | CA2242020716 | TUBB3 | c.1203G= (p.Glu401=) n.4624G= c.987G= (p.Glu329=) c.277+2076G= (n.277+2076G=) c.*1288G= (n.*1288G=) c.2244G= (p.Glu748=) | |
16 | g.89935654G>T | CA397476954 | TUBB3 | c.1203G>T (p.Glu401Asp) n.4624G>T c.987G>T (p.Glu329Asp) c.277+2076G>T (n.277+2076G>T) c.*1288G>T (n.*1288G>T) c.2244G>T (p.Glu748Asp) | |
16 | g.89935655G>A | CA397476955 | TUBB3 | c.1204G>A (p.Gly402Ser) n.4625G>A c.988G>A (p.Gly330Ser) c.277+2077G>A (n.277+2077G>A) c.*1289G>A (n.*1289G>A) c.2245G>A (p.Gly749Ser) | |
16 | g.89935655G>C | CA397476957 | TUBB3 | c.1204G>C (p.Gly402Arg) n.4625G>C c.988G>C (p.Gly330Arg) c.277+2077G>C (n.277+2077G>C) c.*1289G>C (n.*1289G>C) c.2245G>C (p.Gly749Arg) | |
16 | g.89935655G>T | CA397476956 | TUBB3 | c.1204G>T (p.Gly402Cys) n.4625G>T c.988G>T (p.Gly330Cys) c.277+2077G>T (n.277+2077G>T) c.*1289G>T (n.*1289G>T) c.2245G>T (p.Gly749Cys) | |
16 | g.89935656G>A | CA397476958 | TUBB3 | c.1205G>A (p.Gly402Asp) n.4626G>A c.989G>A (p.Gly330Asp) c.277+2078G>A (n.277+2078G>A) c.*1290G>A (n.*1290G>A) c.2246G>A (p.Gly749Asp) | |
16 | g.89935656G>C | CA397476959 | TUBB3 | c.1205G>C (p.Gly402Ala) n.4626G>C c.989G>C (p.Gly330Ala) c.277+2078G>C (n.277+2078G>C) c.*1290G>C (n.*1290G>C) c.2246G>C (p.Gly749Ala) | |
16 | g.89935656G>T | CA397476960 | TUBB3 | c.1205G>T (p.Gly402Val) n.4626G>T c.989G>T (p.Gly330Val) c.277+2078G>T (n.277+2078G>T) c.*1290G>T (n.*1290G>T) c.2246G>T (p.Gly749Val) | |
16 | g.89935657C>A | CA497194437 | TUBB3 | c.1206C>A (p.Gly402=) n.4627C>A c.990C>A (p.Gly330=) c.277+2079C>A (n.277+2079C>A) c.*1291C>A (n.*1291C>A) c.2247C>A (p.Gly749=) | |
16 | g.89935657C= | CA2242020720 | TUBB3 | c.1206C= (p.Gly402=) n.4627C= c.990C= (p.Gly330=) c.277+2079C= (n.277+2079C=) c.*1291C= (n.*1291C=) c.2247C= (p.Gly749=) | |
16 | g.89935657C>G | CA497194438 | TUBB3 | c.1206C>G (p.Gly402=) n.4627C>G c.990C>G (p.Gly330=) c.277+2079C>G (n.277+2079C>G) c.*1291C>G (n.*1291C>G) c.2247C>G (p.Gly749=) | gnomAD v4 |
16 | g.89935657C>T | CA8256221 | TUBB3 | c.1206C>T (p.Gly402=) n.4627C>T c.990C>T (p.Gly330=) c.277+2079C>T (n.277+2079C>T) c.*1291C>T (n.*1291C>T) c.2247C>T (p.Gly749=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.89935658A>C | CA397476961 | TUBB3 | c.1207A>C (p.Met403Leu) n.4628A>C c.991A>C (p.Met331Leu) c.277+2080A>C (n.277+2080A>C) c.*1292A>C (n.*1292A>C) c.2248A>C (p.Met750Leu) | |
16 | g.89935658A>G | CA397476962 | TUBB3 | c.1207A>G (p.Met403Val) n.4628A>G c.991A>G (p.Met331Val) c.277+2080A>G (n.277+2080A>G) c.*1292A>G (n.*1292A>G) c.2248A>G (p.Met750Val) | |
16 | g.89935658A>T | CA397476963 | TUBB3 | c.1207A>T (p.Met403Leu) n.4628A>T c.991A>T (p.Met331Leu) c.277+2080A>T (n.277+2080A>T) c.*1292A>T (n.*1292A>T) c.2248A>T (p.Met750Leu) | |
16 | g.89935659T>A | CA397476964 | TUBB3 | c.1208T>A (p.Met403Lys) n.4629T>A c.992T>A (p.Met331Lys) c.277+2081T>A (n.277+2081T>A) c.*1293T>A (n.*1293T>A) c.2249T>A (p.Met750Lys) | |
16 | g.89935659T>C | CA397476965 | TUBB3 | c.1208T>C (p.Met403Thr) n.4629T>C c.992T>C (p.Met331Thr) c.277+2081T>C (n.277+2081T>C) c.*1293T>C (n.*1293T>C) c.2249T>C (p.Met750Thr) | COSMIC |
16 | g.89935659T>G | CA397476966 | TUBB3 | c.1208T>G (p.Met403Arg) n.4629T>G c.992T>G (p.Met331Arg) c.277+2081T>G (n.277+2081T>G) c.*1293T>G (n.*1293T>G) c.2249T>G (p.Met750Arg) | |
16 | g.89935660G>A | CA397476967 | TUBB3 | c.1209G>A (p.Met403Ile) n.4630G>A c.993G>A (p.Met331Ile) c.277+2082G>A (n.277+2082G>A) c.*1294G>A (n.*1294G>A) c.2250G>A (p.Met750Ile) | |
16 | g.89935660G>C | CA397476968 | TUBB3 | c.1209G>C (p.Met403Ile) n.4630G>C c.993G>C (p.Met331Ile) c.277+2082G>C (n.277+2082G>C) c.*1294G>C (n.*1294G>C) c.2250G>C (p.Met750Ile) | ClinVar dbSNP |
16 | g.89935660G= | CA2242020727 | TUBB3 | c.1209G= (p.Met403=) n.4630G= c.993G= (p.Met331=) c.277+2082G= (n.277+2082G=) c.*1294G= (n.*1294G=) c.2250G= (p.Met750=) | |
16 | g.89935660G>T | CA397476969 | TUBB3 | c.1209G>T (p.Met403Ile) n.4630G>T c.993G>T (p.Met331Ile) c.277+2082G>T (n.277+2082G>T) c.*1294G>T (n.*1294G>T) c.2250G>T (p.Met750Ile) | |
16 | g.89935660_89935661insAG | CA2576104232 | TUBB3 | c.1209_1210insAG (p.Asp404ArgfsTer13) n.4630_4631insAG c.993_994insAG (p.Asp332ArgfsTer13) c.277+2082_277+2083insAG (n.277+2082_277+2083insAG) c.*1294_*1295insAG (n.*1294_*1295insAG) c.2250_2251insAG (p.Asp751ArgfsTer13) | |
16 | g.89935661G>A | CA397476972 | TUBB3 | c.1210G>A (p.Asp404Asn) n.4631G>A c.994G>A (p.Asp332Asn) c.277+2083G>A (n.277+2083G>A) c.*1295G>A (n.*1295G>A) c.2251G>A (p.Asp751Asn) | |
16 | g.89935661G>C | CA397476970 | TUBB3 | c.1210G>C (p.Asp404His) n.4631G>C c.994G>C (p.Asp332His) c.277+2083G>C (n.277+2083G>C) c.*1295G>C (n.*1295G>C) c.2251G>C (p.Asp751His) | |
16 | g.89935661G>T | CA397476971 | TUBB3 | c.1210G>T (p.Asp404Tyr) n.4631G>T c.994G>T (p.Asp332Tyr) c.277+2083G>T (n.277+2083G>T) c.*1295G>T (n.*1295G>T) c.2251G>T (p.Asp751Tyr) | |
16 | g.89935662A>C | CA397476973 | TUBB3 | c.1211A>C (p.Asp404Ala) n.4632A>C c.995A>C (p.Asp332Ala) c.277+2084A>C (n.277+2084A>C) c.*1296A>C (n.*1296A>C) c.2252A>C (p.Asp751Ala) | |
16 | g.89935662A>G | CA397476974 | TUBB3 | c.1211A>G (p.Asp404Gly) n.4632A>G c.995A>G (p.Asp332Gly) c.277+2084A>G (n.277+2084A>G) c.*1296A>G (n.*1296A>G) c.2252A>G (p.Asp751Gly) | |
16 | g.89935662A>T | CA397476975 | TUBB3 | c.1211A>T (p.Asp404Val) n.4632A>T c.995A>T (p.Asp332Val) c.277+2084A>T (n.277+2084A>T) c.*1296A>T (n.*1296A>T) c.2252A>T (p.Asp751Val) | |
16 | g.89935663C>A | CA397476976 | TUBB3 | c.1212C>A (p.Asp404Glu) n.4633C>A c.996C>A (p.Asp332Glu) c.277+2085C>A (n.277+2085C>A) c.*1297C>A (n.*1297C>A) c.2253C>A (p.Asp751Glu) | gnomAD v4 |
16 | g.89935663C= | CA2242020730 | TUBB3 | c.1212C= (p.Asp404=) n.4633C= c.996C= (p.Asp332=) c.277+2085C= (n.277+2085C=) c.*1297C= (n.*1297C=) c.2253C= (p.Asp751=) | |
16 | g.89935663C>G | CA397476977 | TUBB3 | c.1212C>G (p.Asp404Glu) n.4633C>G c.996C>G (p.Asp332Glu) c.277+2085C>G (n.277+2085C>G) c.*1297C>G (n.*1297C>G) c.2253C>G (p.Asp751Glu) | |
16 | g.89935663C>T | CA8256222 | TUBB3 | c.1212C>T (p.Asp404=) n.4633C>T c.996C>T (p.Asp332=) c.277+2085C>T (n.277+2085C>T) c.*1297C>T (n.*1297C>T) c.2253C>T (p.Asp751=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935664G>A | CA397476978 | TUBB3 | c.1213G>A (p.Glu405Lys) n.4634G>A c.997G>A (p.Glu333Lys) c.277+2086G>A (n.277+2086G>A) c.*1298G>A (n.*1298G>A) c.2254G>A (p.Glu752Lys) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.89935664G>C | CA397476979 | TUBB3 | c.1213G>C (p.Glu405Gln) n.4634G>C c.997G>C (p.Glu333Gln) c.277+2086G>C (n.277+2086G>C) c.*1298G>C (n.*1298G>C) c.2254G>C (p.Glu752Gln) | |
16 | g.89935664G= | CA2242020732 | TUBB3 | c.1213G= (p.Glu405=) n.4634G= c.997G= (p.Glu333=) c.277+2086G= (n.277+2086G=) c.*1298G= (n.*1298G=) c.2254G= (p.Glu752=) | |
16 | g.89935664G>T | CA397476980 | TUBB3 | c.1213G>T (p.Glu405Ter) n.4634G>T c.997G>T (p.Glu333Ter) c.277+2086G>T (n.277+2086G>T) c.*1298G>T (n.*1298G>T) c.2254G>T (p.Glu752Ter) | |
16 | g.89935665A>C | CA397476981 | TUBB3 | c.1214A>C (p.Glu405Ala) n.4635A>C c.998A>C (p.Glu333Ala) c.277+2087A>C (n.277+2087A>C) c.*1299A>C (n.*1299A>C) c.2255A>C (p.Glu752Ala) | |
16 | g.89935665A>G | CA397476982 | TUBB3 | c.1214A>G (p.Glu405Gly) n.4635A>G c.998A>G (p.Glu333Gly) c.277+2087A>G (n.277+2087A>G) c.*1299A>G (n.*1299A>G) c.2255A>G (p.Glu752Gly) | |
16 | g.89935665A>T | CA397476983 | TUBB3 | c.1214A>T (p.Glu405Val) n.4635A>T c.998A>T (p.Glu333Val) c.277+2087A>T (n.277+2087A>T) c.*1299A>T (n.*1299A>T) c.2255A>T (p.Glu752Val) | |
16 | g.89935666G>A | CA173787 | TUBB3 | c.1215G>A (p.Glu405=) n.4636G>A c.999G>A (p.Glu333=) c.277+2088G>A (n.277+2088G>A) c.*1300G>A (n.*1300G>A) c.2256G>A (p.Glu752=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935666G>C | CA397476985 | TUBB3 | c.1215G>C (p.Glu405Asp) n.4636G>C c.999G>C (p.Glu333Asp) c.277+2088G>C (n.277+2088G>C) c.*1300G>C (n.*1300G>C) c.2256G>C (p.Glu752Asp) | |
16 | g.89935666G= | CA2242020735 | TUBB3 | c.1215G= (p.Glu405=) n.4636G= c.999G= (p.Glu333=) c.277+2088G= (n.277+2088G=) c.*1300G= (n.*1300G=) c.2256G= (p.Glu752=) | |
16 | g.89935666G>T | CA397476984 | TUBB3 | c.1215G>T (p.Glu405Asp) n.4636G>T c.999G>T (p.Glu333Asp) c.277+2088G>T (n.277+2088G>T) c.*1300G>T (n.*1300G>T) c.2256G>T (p.Glu752Asp) | |
16 | g.89935667A= | CA2242020736 | TUBB3 | c.1216A= (p.Met406=) n.4637A= c.1000A= (p.Met334=) c.277+2089A= (n.277+2089A=) c.*1301A= (n.*1301A=) c.2257A= (p.Met753=) | |
16 | g.89935667A>C | CA397476986 | TUBB3 | c.1216A>C (p.Met406Leu) n.4637A>C c.1000A>C (p.Met334Leu) c.277+2089A>C (n.277+2089A>C) c.*1301A>C (n.*1301A>C) c.2257A>C (p.Met753Leu) | |
16 | g.89935667A>G | CA397476988 | TUBB3 | c.1216A>G (p.Met406Val) n.4637A>G c.1000A>G (p.Met334Val) c.277+2089A>G (n.277+2089A>G) c.*1301A>G (n.*1301A>G) c.2257A>G (p.Met753Val) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.89935667A>T | CA397476987 | TUBB3 | c.1216A>T (p.Met406Leu) n.4637A>T c.1000A>T (p.Met334Leu) c.277+2089A>T (n.277+2089A>T) c.*1301A>T (n.*1301A>T) c.2257A>T (p.Met753Leu) | |
16 | g.89935668T>A | CA397476989 | TUBB3 | c.1217T>A (p.Met406Lys) n.4638T>A c.1001T>A (p.Met334Lys) c.277+2090T>A (n.277+2090T>A) c.*1302T>A (n.*1302T>A) c.2258T>A (p.Met753Lys) | |
16 | g.89935668T>C | CA397476990 | TUBB3 | c.1217T>C (p.Met406Thr) n.4638T>C c.1001T>C (p.Met334Thr) c.277+2090T>C (n.277+2090T>C) c.*1302T>C (n.*1302T>C) c.2258T>C (p.Met753Thr) | |
16 | g.89935668T>G | CA397476991 | TUBB3 | c.1217T>G (p.Met406Arg) n.4638T>G c.1001T>G (p.Met334Arg) c.277+2090T>G (n.277+2090T>G) c.*1302T>G (n.*1302T>G) c.2258T>G (p.Met753Arg) | |
16 | g.89935669G>A | CA397476992 | TUBB3 | c.1218G>A (p.Met406Ile) n.4639G>A c.1002G>A (p.Met334Ile) c.277+2091G>A (n.277+2091G>A) c.*1303G>A (n.*1303G>A) c.2259G>A (p.Met753Ile) | dbSNP |
16 | g.89935669G>C | CA397476993 | TUBB3 | c.1218G>C (p.Met406Ile) n.4639G>C c.1002G>C (p.Met334Ile) c.277+2091G>C (n.277+2091G>C) c.*1303G>C (n.*1303G>C) c.2259G>C (p.Met753Ile) | |
16 | g.89935669G= | CA2242020738 | TUBB3 | c.1218G= (p.Met406=) n.4639G= c.1002G= (p.Met334=) c.277+2091G= (n.277+2091G=) c.*1303G= (n.*1303G=) c.2259G= (p.Met753=) | |
16 | g.89935669G>T | CA397476994 | TUBB3 | c.1218G>T (p.Met406Ile) n.4639G>T c.1002G>T (p.Met334Ile) c.277+2091G>T (n.277+2091G>T) c.*1303G>T (n.*1303G>T) c.2259G>T (p.Met753Ile) | |
16 | g.89935670G>A | CA397476995 | TUBB3 | c.1219G>A (p.Glu407Lys) n.4640G>A c.1003G>A (p.Glu335Lys) c.277+2092G>A (n.277+2092G>A) c.*1304G>A (n.*1304G>A) c.2260G>A (p.Glu754Lys) | |
16 | g.89935670G>C | CA397476996 | TUBB3 | c.1219G>C (p.Glu407Gln) n.4640G>C c.1003G>C (p.Glu335Gln) c.277+2092G>C (n.277+2092G>C) c.*1304G>C (n.*1304G>C) c.2260G>C (p.Glu754Gln) | |
16 | g.89935670G>T | CA397476997 | TUBB3 | c.1219G>T (p.Glu407Ter) n.4640G>T c.1003G>T (p.Glu335Ter) c.277+2092G>T (n.277+2092G>T) c.*1304G>T (n.*1304G>T) c.2260G>T (p.Glu754Ter) | |
16 | g.89935671A>C | CA397476998 | TUBB3 | c.1220A>C (p.Glu407Ala) n.4641A>C c.1004A>C (p.Glu335Ala) c.277+2093A>C (n.277+2093A>C) c.*1305A>C (n.*1305A>C) c.2261A>C (p.Glu754Ala) | |
16 | g.89935671A>G | CA397476999 | TUBB3 | c.1220A>G (p.Glu407Gly) n.4641A>G c.1004A>G (p.Glu335Gly) c.277+2093A>G (n.277+2093A>G) c.*1305A>G (n.*1305A>G) c.2261A>G (p.Glu754Gly) | |
16 | g.89935671A>T | CA397477000 | TUBB3 | c.1220A>T (p.Glu407Val) n.4641A>T c.1004A>T (p.Glu335Val) c.277+2093A>T (n.277+2093A>T) c.*1305A>T (n.*1305A>T) c.2261A>T (p.Glu754Val) | |
16 | g.89935672G>A | CA497194439 | TUBB3 | c.1221G>A (p.Glu407=) n.4642G>A c.1005G>A (p.Glu335=) c.277+2094G>A (n.277+2094G>A) c.*1306G>A (n.*1306G>A) c.2262G>A (p.Glu754=) | |
16 | g.89935672G>C | CA397477002 | TUBB3 | c.1221G>C (p.Glu407Asp) n.4642G>C c.1005G>C (p.Glu335Asp) c.277+2094G>C (n.277+2094G>C) c.*1306G>C (n.*1306G>C) c.2262G>C (p.Glu754Asp) | |
16 | g.89935672G>T | CA397477001 | TUBB3 | c.1221G>T (p.Glu407Asp) n.4642G>T c.1005G>T (p.Glu335Asp) c.277+2094G>T (n.277+2094G>T) c.*1306G>T (n.*1306G>T) c.2262G>T (p.Glu754Asp) | |
16 | g.89935673T>A | CA397477003 | TUBB3 | c.1222T>A (p.Phe408Ile) n.4643T>A c.1006T>A (p.Phe336Ile) c.277+2095T>A (n.277+2095T>A) c.*1307T>A (n.*1307T>A) c.2263T>A (p.Phe755Ile) | |
16 | g.89935673T>C | CA397477004 | TUBB3 | c.1222T>C (p.Phe408Leu) n.4643T>C c.1006T>C (p.Phe336Leu) c.277+2095T>C (n.277+2095T>C) c.*1307T>C (n.*1307T>C) c.2263T>C (p.Phe755Leu) | |
16 | g.89935673T>G | CA397477005 | TUBB3 | c.1222T>G (p.Phe408Val) n.4643T>G c.1006T>G (p.Phe336Val) c.277+2095T>G (n.277+2095T>G) c.*1307T>G (n.*1307T>G) c.2263T>G (p.Phe755Val) | |
16 | g.89935674T>A | CA397477006 | TUBB3 | c.1223T>A (p.Phe408Tyr) n.4644T>A c.1007T>A (p.Phe336Tyr) c.277+2096T>A (n.277+2096T>A) c.*1308T>A (n.*1308T>A) c.2264T>A (p.Phe755Tyr) | |
16 | g.89935674T>C | CA397477007 | TUBB3 | c.1223T>C (p.Phe408Ser) n.4644T>C c.1007T>C (p.Phe336Ser) c.277+2096T>C (n.277+2096T>C) c.*1308T>C (n.*1308T>C) c.2264T>C (p.Phe755Ser) | |
16 | g.89935674T>G | CA397477008 | TUBB3 | c.1223T>G (p.Phe408Cys) n.4644T>G c.1007T>G (p.Phe336Cys) c.277+2096T>G (n.277+2096T>G) c.*1308T>G (n.*1308T>G) c.2264T>G (p.Phe755Cys) | |
16 | g.89935675C>A | CA397477009 | TUBB3 | c.1224C>A (p.Phe408Leu) n.4645C>A c.1008C>A (p.Phe336Leu) c.277+2097C>A (n.277+2097C>A) c.*1309C>A (n.*1309C>A) c.2265C>A (p.Phe755Leu) | |
16 | g.89935675C>G | CA397477010 | TUBB3 | c.1224C>G (p.Phe408Leu) n.4645C>G c.1008C>G (p.Phe336Leu) c.277+2097C>G (n.277+2097C>G) c.*1309C>G (n.*1309C>G) c.2265C>G (p.Phe755Leu) | |
16 | g.89935675C>T | CA497194440 | TUBB3 | c.1224C>T (p.Phe408=) n.4645C>T c.1008C>T (p.Phe336=) c.277+2097C>T (n.277+2097C>T) c.*1309C>T (n.*1309C>T) c.2265C>T (p.Phe755=) | |
16 | g.89935676A>C | CA397477011 | TUBB3 | c.1225A>C (p.Thr409Pro) n.4646A>C c.1009A>C (p.Thr337Pro) c.277+2098A>C (n.277+2098A>C) c.*1310A>C (n.*1310A>C) c.2266A>C (p.Thr756Pro) | |
16 | g.89935676A>G | CA397477012 | TUBB3 | c.1225A>G (p.Thr409Ala) n.4646A>G c.1009A>G (p.Thr337Ala) c.277+2098A>G (n.277+2098A>G) c.*1310A>G (n.*1310A>G) c.2266A>G (p.Thr756Ala) | gnomAD v4 |
16 | g.89935676A>T | CA397477013 | TUBB3 | c.1225A>T (p.Thr409Ser) n.4646A>T c.1009A>T (p.Thr337Ser) c.277+2098A>T (n.277+2098A>T) c.*1310A>T (n.*1310A>T) c.2266A>T (p.Thr756Ser) | |
16 | g.89935677C>A | CA397477016 | TUBB3 | c.1226C>A (p.Thr409Asn) n.4647C>A c.1010C>A (p.Thr337Asn) c.277+2099C>A (n.277+2099C>A) c.*1311C>A (n.*1311C>A) c.2267C>A (p.Thr756Asn) | |
16 | g.89935677C= | CA2242020740 | TUBB3 | c.1226C= (p.Thr409=) n.4647C= c.1010C= (p.Thr337=) c.277+2099C= (n.277+2099C=) c.*1311C= (n.*1311C=) c.2267C= (p.Thr756=) | |
16 | g.89935677C>G | CA397477015 | TUBB3 | c.1226C>G (p.Thr409Ser) n.4647C>G c.1010C>G (p.Thr337Ser) c.277+2099C>G (n.277+2099C>G) c.*1311C>G (n.*1311C>G) c.2267C>G (p.Thr756Ser) | |
16 | g.89935677C>T | CA397477014 | TUBB3 | c.1226C>T (p.Thr409Ile) n.4647C>T c.1010C>T (p.Thr337Ile) c.277+2099C>T (n.277+2099C>T) c.*1311C>T (n.*1311C>T) c.2267C>T (p.Thr756Ile) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
16 | g.89935678C>A | CA497194441 | TUBB3 | c.1227C>A (p.Thr409=) n.4648C>A c.1011C>A (p.Thr337=) c.277+2100C>A (n.277+2100C>A) c.*1312C>A (n.*1312C>A) c.2268C>A (p.Thr756=) | |
16 | g.89935678C= | CA2242020743 | TUBB3 | c.1227C= (p.Thr409=) n.4648C= c.1011C= (p.Thr337=) c.277+2100C= (n.277+2100C=) c.*1312C= (n.*1312C=) c.2268C= (p.Thr756=) | |
16 | g.89935678C>G | CA497194442 | TUBB3 | c.1227C>G (p.Thr409=) n.4648C>G c.1011C>G (p.Thr337=) c.277+2100C>G (n.277+2100C>G) c.*1312C>G (n.*1312C>G) c.2268C>G (p.Thr756=) | |
16 | g.89935678C>T | CA8256223 | TUBB3 | c.1227C>T (p.Thr409=) n.4648C>T c.1011C>T (p.Thr337=) c.277+2100C>T (n.277+2100C>T) c.*1312C>T (n.*1312C>T) c.2268C>T (p.Thr756=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
16 | g.89935679G>A | CA213335 | TUBB3 | c.1228G>A (p.Glu410Lys) n.4649G>A c.1012G>A (p.Glu338Lys) c.277+2101G>A (n.277+2101G>A) c.*1313G>A (n.*1313G>A) c.2269G>A (p.Glu757Lys) | ClinVar dbSNP |
16 | g.89935679G>C | CA397477017 | TUBB3 | c.1228G>C (p.Glu410Gln) n.4649G>C c.1012G>C (p.Glu338Gln) c.277+2101G>C (n.277+2101G>C) c.*1313G>C (n.*1313G>C) c.2269G>C (p.Glu757Gln) | dbSNP |
16 | g.89935679G= | CA2242020746 | TUBB3 | c.1228G= (p.Glu410=) n.4649G= c.1012G= (p.Glu338=) c.277+2101G= (n.277+2101G=) c.*1313G= (n.*1313G=) c.2269G= (p.Glu757=) | |
16 | g.89935679G>T | CA397477018 | TUBB3 | c.1228G>T (p.Glu410Ter) n.4649G>T c.1012G>T (p.Glu338Ter) c.277+2101G>T (n.277+2101G>T) c.*1313G>T (n.*1313G>T) c.2269G>T (p.Glu757Ter) | |
16 | g.89935680A>C | CA397477019 | TUBB3 | c.1229A>C (p.Glu410Ala) n.4650A>C c.1013A>C (p.Glu338Ala) c.277+2102A>C (n.277+2102A>C) c.*1314A>C (n.*1314A>C) c.2270A>C (p.Glu757Ala) | |
16 | g.89935680A>G | CA397477020 | TUBB3 | c.1229A>G (p.Glu410Gly) n.4650A>G c.1013A>G (p.Glu338Gly) c.277+2102A>G (n.277+2102A>G) c.*1314A>G (n.*1314A>G) c.2270A>G (p.Glu757Gly) | |
16 | g.89935680A>T | CA397477021 | TUBB3 | c.1229A>T (p.Glu410Val) n.4650A>T c.1013A>T (p.Glu338Val) c.277+2102A>T (n.277+2102A>T) c.*1314A>T (n.*1314A>T) c.2270A>T (p.Glu757Val) | |
16 | g.89935681G>A | CA497194443 | TUBB3 | c.1230G>A (p.Glu410=) n.4651G>A c.1014G>A (p.Glu338=) c.277+2103G>A (n.277+2103G>A) c.*1315G>A (n.*1315G>A) c.2271G>A (p.Glu757=) | gnomAD v4 |
16 | g.89935681G>C | CA397477022 | TUBB3 | c.1230G>C (p.Glu410Asp) n.4651G>C c.1014G>C (p.Glu338Asp) c.277+2103G>C (n.277+2103G>C) c.*1315G>C (n.*1315G>C) c.2271G>C (p.Glu757Asp) | |
16 | g.89935681G>T | CA397477023 | TUBB3 | c.1230G>T (p.Glu410Asp) n.4651G>T c.1014G>T (p.Glu338Asp) c.277+2103G>T (n.277+2103G>T) c.*1315G>T (n.*1315G>T) c.2271G>T (p.Glu757Asp) | |
16 | g.89935682G>A | CA397477024 | TUBB3 | c.1231G>A (p.Ala411Thr) n.4652G>A c.1015G>A (p.Ala339Thr) c.277+2104G>A (n.277+2104G>A) c.*1316G>A (n.*1316G>A) c.2272G>A (p.Ala758Thr) | |
16 | g.89935682G>C | CA397477025 | TUBB3 | c.1231G>C (p.Ala411Pro) n.4652G>C c.1015G>C (p.Ala339Pro) c.277+2104G>C (n.277+2104G>C) c.*1316G>C (n.*1316G>C) c.2272G>C (p.Ala758Pro) | |
16 | g.89935682G>T | CA397477026 | TUBB3 | c.1231G>T (p.Ala411Ser) n.4652G>T c.1015G>T (p.Ala339Ser) c.277+2104G>T (n.277+2104G>T) c.*1316G>T (n.*1316G>T) c.2272G>T (p.Ala758Ser) | |
16 | g.89935683C>A | CA397477029 | TUBB3 | c.1232C>A (p.Ala411Asp) n.4653C>A c.1016C>A (p.Ala339Asp) c.277+2105C>A (n.277+2105C>A) c.*1317C>A (n.*1317C>A) c.2273C>A (p.Ala758Asp) | |
16 | g.89935683C>G | CA397477028 | TUBB3 | c.1232C>G (p.Ala411Gly) n.4653C>G c.1016C>G (p.Ala339Gly) c.277+2105C>G (n.277+2105C>G) c.*1317C>G (n.*1317C>G) c.2273C>G (p.Ala758Gly) | |
16 | g.89935683C>T | CA397477027 | TUBB3 | c.1232C>T (p.Ala411Val) n.4653C>T c.1016C>T (p.Ala339Val) c.277+2105C>T (n.277+2105C>T) c.*1317C>T (n.*1317C>T) c.2273C>T (p.Ala758Val) | |
16 | g.89935684C>A | CA497194444 | TUBB3 | c.1233C>A (p.Ala411=) n.4654C>A c.1017C>A (p.Ala339=) c.277+2106C>A (n.277+2106C>A) c.*1318C>A (n.*1318C>A) c.2274C>A (p.Ala758=) | gnomAD v4 |
16 | g.89935684C= | CA2242020754 | TUBB3 | c.1233C= (p.Ala411=) n.4654C= c.1017C= (p.Ala339=) c.277+2106C= (n.277+2106C=) c.*1318C= (n.*1318C=) c.2274C= (p.Ala758=) | |
16 | g.89935684C>G | CA497194445 | TUBB3 | c.1233C>G (p.Ala411=) n.4654C>G c.1017C>G (p.Ala339=) c.277+2106C>G (n.277+2106C>G) c.*1318C>G (n.*1318C>G) c.2274C>G (p.Ala758=) | |
16 | g.89935684C>T | CA8256224 | TUBB3 | c.1233C>T (p.Ala411=) n.4654C>T c.1017C>T (p.Ala339=) c.277+2106C>T (n.277+2106C>T) c.*1318C>T (n.*1318C>T) c.2274C>T (p.Ala758=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935685G>A | CA397477030 | TUBB3 | c.1234G>A (p.Glu412Lys) n.4655G>A c.1018G>A (p.Glu340Lys) c.277+2107G>A (n.277+2107G>A) c.*1319G>A (n.*1319G>A) c.2275G>A (p.Glu759Lys) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.89935685G>C | CA397477031 | TUBB3 | c.1234G>C (p.Glu412Gln) n.4655G>C c.1018G>C (p.Glu340Gln) c.277+2107G>C (n.277+2107G>C) c.*1319G>C (n.*1319G>C) c.2275G>C (p.Glu759Gln) | |
16 | g.89935685G= | CA2242020756 | TUBB3 | c.1234G= (p.Glu412=) n.4655G= c.1018G= (p.Glu340=) c.277+2107G= (n.277+2107G=) c.*1319G= (n.*1319G=) c.2275G= (p.Glu759=) | |
16 | g.89935685G>T | CA397477032 | TUBB3 | c.1234G>T (p.Glu412Ter) n.4655G>T c.1018G>T (p.Glu340Ter) c.277+2107G>T (n.277+2107G>T) c.*1319G>T (n.*1319G>T) c.2275G>T (p.Glu759Ter) | |
16 | g.89935686A>C | CA397477033 | TUBB3 | c.1235A>C (p.Glu412Ala) n.4656A>C c.1019A>C (p.Glu340Ala) c.277+2108A>C (n.277+2108A>C) c.*1320A>C (n.*1320A>C) c.2276A>C (p.Glu759Ala) | |
16 | g.89935686A>G | CA397477034 | TUBB3 | c.1235A>G (p.Glu412Gly) n.4656A>G c.1019A>G (p.Glu340Gly) c.277+2108A>G (n.277+2108A>G) c.*1320A>G (n.*1320A>G) c.2276A>G (p.Glu759Gly) | |
16 | g.89935686A>T | CA397477035 | TUBB3 | c.1235A>T (p.Glu412Val) n.4656A>T c.1019A>T (p.Glu340Val) c.277+2108A>T (n.277+2108A>T) c.*1320A>T (n.*1320A>T) c.2276A>T (p.Glu759Val) | |
16 | g.89935687G>A | CA497194446 | TUBB3 | c.1236G>A (p.Glu412=) n.4657G>A c.1020G>A (p.Glu340=) c.277+2109G>A (n.277+2109G>A) c.*1321G>A (n.*1321G>A) c.2277G>A (p.Glu759=) | gnomAD v4 |
16 | g.89935687G>C | CA397477036 | TUBB3 | c.1236G>C (p.Glu412Asp) n.4657G>C c.1020G>C (p.Glu340Asp) c.277+2109G>C (n.277+2109G>C) c.*1321G>C (n.*1321G>C) c.2277G>C (p.Glu759Asp) | |
16 | g.89935687G>T | CA397477037 | TUBB3 | c.1236G>T (p.Glu412Asp) n.4657G>T c.1020G>T (p.Glu340Asp) c.277+2109G>T (n.277+2109G>T) c.*1321G>T (n.*1321G>T) c.2277G>T (p.Glu759Asp) | |
16 | g.89935688A>C | CA397477038 | TUBB3 | c.1237A>C (p.Ser413Arg) n.4658A>C c.1021A>C (p.Ser341Arg) c.277+2110A>C (n.277+2110A>C) c.*1322A>C (n.*1322A>C) c.2278A>C (p.Ser760Arg) | |
16 | g.89935688A>G | CA397477039 | TUBB3 | c.1237A>G (p.Ser413Gly) n.4658A>G c.1021A>G (p.Ser341Gly) c.277+2110A>G (n.277+2110A>G) c.*1322A>G (n.*1322A>G) c.2278A>G (p.Ser760Gly) | |
16 | g.89935688A>T | CA397477040 | TUBB3 | c.1237A>T (p.Ser413Cys) n.4658A>T c.1021A>T (p.Ser341Cys) c.277+2110A>T (n.277+2110A>T) c.*1322A>T (n.*1322A>T) c.2278A>T (p.Ser760Cys) | |
16 | g.89935689G>A | CA397477041 | TUBB3 | c.1238G>A (p.Ser413Asn) n.4659G>A c.1022G>A (p.Ser341Asn) c.277+2111G>A (n.277+2111G>A) c.*1323G>A (n.*1323G>A) c.2279G>A (p.Ser760Asn) | |
16 | g.89935689G>C | CA397477043 | TUBB3 | c.1238G>C (p.Ser413Thr) n.4659G>C c.1022G>C (p.Ser341Thr) c.277+2111G>C (n.277+2111G>C) c.*1323G>C (n.*1323G>C) c.2279G>C (p.Ser760Thr) | |
16 | g.89935689G>T | CA397477042 | TUBB3 | c.1238G>T (p.Ser413Ile) n.4659G>T c.1022G>T (p.Ser341Ile) c.277+2111G>T (n.277+2111G>T) c.*1323G>T (n.*1323G>T) c.2279G>T (p.Ser760Ile) | |
16 | g.89935690C>A | CA397477044 | TUBB3 | c.1239C>A (p.Ser413Arg) n.4660C>A c.1023C>A (p.Ser341Arg) c.277+2112C>A (n.277+2112C>A) c.*1324C>A (n.*1324C>A) c.2280C>A (p.Ser760Arg) | |
16 | g.89935690C>G | CA397477045 | TUBB3 | c.1239C>G (p.Ser413Arg) n.4660C>G c.1023C>G (p.Ser341Arg) c.277+2112C>G (n.277+2112C>G) c.*1324C>G (n.*1324C>G) c.2280C>G (p.Ser760Arg) | ClinVar dbSNP gnomAD v4 |
16 | g.89935690C>T | CA497194447 | TUBB3 | c.1239C>T (p.Ser413=) n.4660C>T c.1023C>T (p.Ser341=) c.277+2112C>T (n.277+2112C>T) c.*1324C>T (n.*1324C>T) c.2280C>T (p.Ser760=) | gnomAD v4 |
16 | g.89935691A>C | CA397477046 | TUBB3 | c.1240A>C (p.Asn414His) n.4661A>C c.1024A>C (p.Asn342His) c.277+2113A>C (n.277+2113A>C) c.*1325A>C (n.*1325A>C) c.2281A>C (p.Asn761His) | |
16 | g.89935691A>G | CA397477048 | TUBB3 | c.1240A>G (p.Asn414Asp) n.4661A>G c.1024A>G (p.Asn342Asp) c.277+2113A>G (n.277+2113A>G) c.*1325A>G (n.*1325A>G) c.2281A>G (p.Asn761Asp) | |
16 | g.89935691A>T | CA397477047 | TUBB3 | c.1240A>T (p.Asn414Tyr) n.4661A>T c.1024A>T (p.Asn342Tyr) c.277+2113A>T (n.277+2113A>T) c.*1325A>T (n.*1325A>T) c.2281A>T (p.Asn761Tyr) | |
16 | g.89935692A>C | CA397477049 | TUBB3 | c.1241A>C (p.Asn414Thr) n.4662A>C c.1025A>C (p.Asn342Thr) c.277+2114A>C (n.277+2114A>C) c.*1326A>C (n.*1326A>C) c.2282A>C (p.Asn761Thr) | |
16 | g.89935692A>G | CA397477051 | TUBB3 | c.1241A>G (p.Asn414Ser) n.4662A>G c.1025A>G (p.Asn342Ser) c.277+2114A>G (n.277+2114A>G) c.*1326A>G (n.*1326A>G) c.2282A>G (p.Asn761Ser) | |
16 | g.89935692A>T | CA397477050 | TUBB3 | c.1241A>T (p.Asn414Ile) n.4662A>T c.1025A>T (p.Asn342Ile) c.277+2114A>T (n.277+2114A>T) c.*1326A>T (n.*1326A>T) c.2282A>T (p.Asn761Ile) | |
16 | g.89935693C>A | CA397477052 | TUBB3 | c.1242C>A (p.Asn414Lys) n.4663C>A c.1026C>A (p.Asn342Lys) c.277+2115C>A (n.277+2115C>A) c.*1327C>A (n.*1327C>A) c.2283C>A (p.Asn761Lys) | |
16 | g.89935693C>G | CA397477053 | TUBB3 | c.1242C>G (p.Asn414Lys) n.4663C>G c.1026C>G (p.Asn342Lys) c.277+2115C>G (n.277+2115C>G) c.*1327C>G (n.*1327C>G) c.2283C>G (p.Asn761Lys) | |
16 | g.89935693C>T | CA497194449 | TUBB3 | c.1242C>T (p.Asn414=) n.4663C>T c.1026C>T (p.Asn342=) c.277+2115C>T (n.277+2115C>T) c.*1327C>T (n.*1327C>T) c.2283C>T (p.Asn761=) | gnomAD v4 |
16 | g.89935694A= | CA2242020758 | TUBB3 | c.1243A= (p.Met415=) n.4664A= c.1027A= (p.Met343=) c.277+2116A= (n.277+2116A=) c.*1328A= (n.*1328A=) c.2284A= (p.Met762=) | |
16 | g.89935694A>C | CA397477054 | TUBB3 | c.1243A>C (p.Met415Leu) n.4664A>C c.1027A>C (p.Met343Leu) c.277+2116A>C (n.277+2116A>C) c.*1328A>C (n.*1328A>C) c.2284A>C (p.Met762Leu) | |
16 | g.89935694A>G | CA397477055 | TUBB3 | c.1243A>G (p.Met415Val) n.4664A>G c.1027A>G (p.Met343Val) c.277+2116A>G (n.277+2116A>G) c.*1328A>G (n.*1328A>G) c.2284A>G (p.Met762Val) | dbSNP gnomAD v4 |
16 | g.89935694A>T | CA397477056 | TUBB3 | c.1243A>T (p.Met415Leu) n.4664A>T c.1027A>T (p.Met343Leu) c.277+2116A>T (n.277+2116A>T) c.*1328A>T (n.*1328A>T) c.2284A>T (p.Met762Leu) | |
16 | g.89935695T>A | CA397477057 | TUBB3 | c.1244T>A (p.Met415Lys) n.4665T>A c.1028T>A (p.Met343Lys) c.277+2117T>A (n.277+2117T>A) c.*1329T>A (n.*1329T>A) c.2285T>A (p.Met762Lys) | |
16 | g.89935695T>C | CA397477058 | TUBB3 | c.1244T>C (p.Met415Thr) n.4665T>C c.1028T>C (p.Met343Thr) c.277+2117T>C (n.277+2117T>C) c.*1329T>C (n.*1329T>C) c.2285T>C (p.Met762Thr) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.89935695T>G | CA397477059 | TUBB3 | c.1244T>G (p.Met415Arg) n.4665T>G c.1028T>G (p.Met343Arg) c.277+2117T>G (n.277+2117T>G) c.*1329T>G (n.*1329T>G) c.2285T>G (p.Met762Arg) | |
16 | g.89935695T= | CA2242020760 | TUBB3 | c.1244T= (p.Met415=) n.4665T= c.1028T= (p.Met343=) c.277+2117T= (n.277+2117T=) c.*1329T= (n.*1329T=) c.2285T= (p.Met762=) | |
16 | g.89935696G>A | CA8256225 | TUBB3 | c.1245G>A (p.Met415Ile) n.4666G>A c.1029G>A (p.Met343Ile) c.277+2118G>A (n.277+2118G>A) c.*1330G>A (n.*1330G>A) c.2286G>A (p.Met762Ile) | dbSNP ExAC gnomAD v2 |
16 | g.89935696G>C | CA397477060 | TUBB3 | c.1245G>C (p.Met415Ile) n.4666G>C c.1029G>C (p.Met343Ile) c.277+2118G>C (n.277+2118G>C) c.*1330G>C (n.*1330G>C) c.2286G>C (p.Met762Ile) | |
16 | g.89935696G= | CA2242020763 | TUBB3 | c.1245G= (p.Met415=) n.4666G= c.1029G= (p.Met343=) c.277+2118G= (n.277+2118G=) c.*1330G= (n.*1330G=) c.2286G= (p.Met762=) | |
16 | g.89935696G>T | CA397477061 | TUBB3 | c.1245G>T (p.Met415Ile) n.4666G>T c.1029G>T (p.Met343Ile) c.277+2118G>T (n.277+2118G>T) c.*1330G>T (n.*1330G>T) c.2286G>T (p.Met762Ile) | |
16 | g.89935697A>C | CA397477064 | TUBB3 | c.1246A>C (p.Asn416His) n.4667A>C c.1030A>C (p.Asn344His) c.277+2119A>C (n.277+2119A>C) c.*1331A>C (n.*1331A>C) c.2287A>C (p.Asn763His) | |
16 | g.89935697A>G | CA397477062 | TUBB3 | c.1246A>G (p.Asn416Asp) n.4667A>G c.1030A>G (p.Asn344Asp) c.277+2119A>G (n.277+2119A>G) c.*1331A>G (n.*1331A>G) c.2287A>G (p.Asn763Asp) | |
16 | g.89935697A>T | CA397477063 | TUBB3 | c.1246A>T (p.Asn416Tyr) n.4667A>T c.1030A>T (p.Asn344Tyr) c.277+2119A>T (n.277+2119A>T) c.*1331A>T (n.*1331A>T) c.2287A>T (p.Asn763Tyr) | |
16 | g.89935698A= | CA2242020764 | TUBB3 | c.1247A= (p.Asn416=) n.4668A= c.1031A= (p.Asn344=) c.277+2120A= (n.277+2120A=) c.*1332A= (n.*1332A=) c.2288A= (p.Asn763=) | |
16 | g.89935698A>C | CA397477065 | TUBB3 | c.1247A>C (p.Asn416Thr) n.4668A>C c.1031A>C (p.Asn344Thr) c.277+2120A>C (n.277+2120A>C) c.*1332A>C (n.*1332A>C) c.2288A>C (p.Asn763Thr) | |
16 | g.89935698A>G | CA397477066 | TUBB3 | c.1247A>G (p.Asn416Ser) n.4668A>G c.1031A>G (p.Asn344Ser) c.277+2120A>G (n.277+2120A>G) c.*1332A>G (n.*1332A>G) c.2288A>G (p.Asn763Ser) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.89935698A>T | CA397477067 | TUBB3 | c.1247A>T (p.Asn416Ile) n.4668A>T c.1031A>T (p.Asn344Ile) c.277+2120A>T (n.277+2120A>T) c.*1332A>T (n.*1332A>T) c.2288A>T (p.Asn763Ile) | |
16 | g.89935699C>A | CA397477068 | TUBB3 | c.1248C>A (p.Asn416Lys) n.4669C>A c.1032C>A (p.Asn344Lys) c.277+2121C>A (n.277+2121C>A) c.*1333C>A (n.*1333C>A) c.2289C>A (p.Asn763Lys) | |
16 | g.89935699C= | CA2242020765 | TUBB3 | c.1248C= (p.Asn416=) n.4669C= c.1032C= (p.Asn344=) c.277+2121C= (n.277+2121C=) c.*1333C= (n.*1333C=) c.2289C= (p.Asn763=) | |
16 | g.89935699C>G | CA397477069 | TUBB3 | c.1248C>G (p.Asn416Lys) n.4669C>G c.1032C>G (p.Asn344Lys) c.277+2121C>G (n.277+2121C>G) c.*1333C>G (n.*1333C>G) c.2289C>G (p.Asn763Lys) | COSMIC |
16 | g.89935699C>T | CA8256226 | TUBB3 | c.1248C>T (p.Asn416=) n.4669C>T c.1032C>T (p.Asn344=) c.277+2121C>T (n.277+2121C>T) c.*1333C>T (n.*1333C>T) c.2289C>T (p.Asn763=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
16 | g.89935700G>A | CA340624 | TUBB3 | c.1249G>A (p.Asp417Asn) n.4670G>A c.1033G>A (p.Asp345Asn) c.277+2122G>A (n.277+2122G>A) c.*1334G>A (n.*1334G>A) c.2290G>A (p.Asp764Asn) | ClinVar dbSNP COSMIC |
16 | g.89935700G>C | CA340622 | TUBB3 | c.1249G>C (p.Asp417His) n.4670G>C c.1033G>C (p.Asp345His) c.277+2122G>C (n.277+2122G>C) c.*1334G>C (n.*1334G>C) c.2290G>C (p.Asp764His) | ClinVar dbSNP |
16 | g.89935700G= | CA2242020768 | TUBB3 | c.1249G= (p.Asp417=) n.4670G= c.1033G= (p.Asp345=) c.277+2122G= (n.277+2122G=) c.*1334G= (n.*1334G=) c.2290G= (p.Asp764=) | |
16 | g.89935700G>T | CA397477070 | TUBB3 | c.1249G>T (p.Asp417Tyr) n.4670G>T c.1033G>T (p.Asp345Tyr) c.277+2122G>T (n.277+2122G>T) c.*1334G>T (n.*1334G>T) c.2290G>T (p.Asp764Tyr) | |
16 | g.89935701A>C | CA397477073 | TUBB3 | c.1250A>C (p.Asp417Ala) n.4671A>C c.1034A>C (p.Asp345Ala) c.277+2123A>C (n.277+2123A>C) c.*1335A>C (n.*1335A>C) c.2291A>C (p.Asp764Ala) | |
16 | g.89935701A>G | CA397477072 | TUBB3 | c.1250A>G (p.Asp417Gly) n.4671A>G c.1034A>G (p.Asp345Gly) c.277+2123A>G (n.277+2123A>G) c.*1335A>G (n.*1335A>G) c.2291A>G (p.Asp764Gly) | gnomAD v4 |
16 | g.89935701A>T | CA397477071 | TUBB3 | c.1250A>T (p.Asp417Val) n.4671A>T c.1034A>T (p.Asp345Val) c.277+2123A>T (n.277+2123A>T) c.*1335A>T (n.*1335A>T) c.2291A>T (p.Asp764Val) | |
16 | g.89935702C>A | CA397477074 | TUBB3 | c.1251C>A (p.Asp417Glu) n.4672C>A c.1035C>A (p.Asp345Glu) c.277+2124C>A (n.277+2124C>A) c.*1336C>A (n.*1336C>A) c.2292C>A (p.Asp764Glu) | |
16 | g.89935702C= | CA2242020770 | TUBB3 | c.1251C= (p.Asp417=) n.4672C= c.1035C= (p.Asp345=) c.277+2124C= (n.277+2124C=) c.*1336C= (n.*1336C=) c.2292C= (p.Asp764=) | |
16 | g.89935702C>G | CA397477075 | TUBB3 | c.1251C>G (p.Asp417Glu) n.4672C>G c.1035C>G (p.Asp345Glu) c.277+2124C>G (n.277+2124C>G) c.*1336C>G (n.*1336C>G) c.2292C>G (p.Asp764Glu) | |
16 | g.89935702C>T | CA8256227 | TUBB3 | c.1251C>T (p.Asp417=) n.4672C>T c.1035C>T (p.Asp345=) c.277+2124C>T (n.277+2124C>T) c.*1336C>T (n.*1336C>T) c.2292C>T (p.Asp764=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.89935703C>A | CA397477076 | TUBB3 | c.1252C>A (p.Leu418Met) n.4673C>A c.1036C>A (p.Leu346Met) c.277+2125C>A (n.277+2125C>A) c.*1337C>A (n.*1337C>A) c.2293C>A (p.Leu765Met) | |
16 | g.89935703C= | CA2242020771 | TUBB3 | c.1252C= (p.Leu418=) n.4673C= c.1036C= (p.Leu346=) c.277+2125C= (n.277+2125C=) c.*1337C= (n.*1337C=) c.2293C= (p.Leu765=) | |
16 | g.89935703C>G | CA397477077 | TUBB3 | c.1252C>G (p.Leu418Val) n.4673C>G c.1036C>G (p.Leu346Val) c.277+2125C>G (n.277+2125C>G) c.*1337C>G (n.*1337C>G) c.2293C>G (p.Leu765Val) | |
16 | g.89935703C>T | CA497194453 | TUBB3 | c.1252C>T (p.Leu418=) n.4673C>T c.1036C>T (p.Leu346=) c.277+2125C>T (n.277+2125C>T) c.*1337C>T (n.*1337C>T) c.2293C>T (p.Leu765=) | dbSNP gnomAD v4 |
16 | g.89935704T>A | CA397477078 | TUBB3 | c.1253T>A (p.Leu418Gln) n.4674T>A c.1037T>A (p.Leu346Gln) c.277+2126T>A (n.277+2126T>A) c.*1338T>A (n.*1338T>A) c.2294T>A (p.Leu765Gln) | |
16 | g.89935704T>C | CA397477079 | TUBB3 | c.1253T>C (p.Leu418Pro) n.4674T>C c.1037T>C (p.Leu346Pro) c.277+2126T>C (n.277+2126T>C) c.*1338T>C (n.*1338T>C) c.2294T>C (p.Leu765Pro) | |
16 | g.89935704T>G | CA397477080 | TUBB3 | c.1253T>G (p.Leu418Arg) n.4674T>G c.1037T>G (p.Leu346Arg) c.277+2126T>G (n.277+2126T>G) c.*1338T>G (n.*1338T>G) c.2294T>G (p.Leu765Arg) | |
16 | g.89935705G>A | CA497194454 | TUBB3 | c.1254G>A (p.Leu418=) n.4675G>A c.1038G>A (p.Leu346=) c.277+2127G>A (n.277+2127G>A) c.*1339G>A (n.*1339G>A) c.2295G>A (p.Leu765=) | |
16 | g.89935705G>C | CA8256228 | TUBB3 | c.1254G>C (p.Leu418=) n.4675G>C c.1038G>C (p.Leu346=) c.277+2127G>C (n.277+2127G>C) c.*1339G>C (n.*1339G>C) c.2295G>C (p.Leu765=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.89935705G= | CA2242020773 | TUBB3 | c.1254G= (p.Leu418=) n.4675G= c.1038G= (p.Leu346=) c.277+2127G= (n.277+2127G=) c.*1339G= (n.*1339G=) c.2295G= (p.Leu765=) | |
16 | g.89935705G>T | CA497194455 | TUBB3 | c.1254G>T (p.Leu418=) n.4675G>T c.1038G>T (p.Leu346=) c.277+2127G>T (n.277+2127G>T) c.*1339G>T (n.*1339G>T) c.2295G>T (p.Leu765=) | |
16 | g.89935706G>A | CA397477081 | TUBB3 | c.1255G>A (p.Val419Met) n.4676G>A c.1039G>A (p.Val347Met) c.277+2128G>A (n.277+2128G>A) c.*1340G>A (n.*1340G>A) c.2296G>A (p.Val766Met) | |
16 | g.89935706G>C | CA397477082 | TUBB3 | c.1255G>C (p.Val419Leu) n.4676G>C c.1039G>C (p.Val347Leu) c.277+2128G>C (n.277+2128G>C) c.*1340G>C (n.*1340G>C) c.2296G>C (p.Val766Leu) | |
16 | g.89935706G>T | CA397477083 | TUBB3 | c.1255G>T (p.Val419Leu) n.4676G>T c.1039G>T (p.Val347Leu) c.277+2128G>T (n.277+2128G>T) c.*1340G>T (n.*1340G>T) c.2296G>T (p.Val766Leu) | gnomAD v4 |
16 | g.89935707T>A | CA397477086 | TUBB3 | c.1256T>A (p.Val419Glu) n.4677T>A c.1040T>A (p.Val347Glu) c.277+2129T>A (n.277+2129T>A) c.*1341T>A (n.*1341T>A) c.2297T>A (p.Val766Glu) | |
16 | g.89935707T>C | CA397477084 | TUBB3 | c.1256T>C (p.Val419Ala) n.4677T>C c.1040T>C (p.Val347Ala) c.277+2129T>C (n.277+2129T>C) c.*1341T>C (n.*1341T>C) c.2297T>C (p.Val766Ala) | |
16 | g.89935707T>G | CA397477085 | TUBB3 | c.1256T>G (p.Val419Gly) n.4677T>G c.1040T>G (p.Val347Gly) c.277+2129T>G (n.277+2129T>G) c.*1341T>G (n.*1341T>G) c.2297T>G (p.Val766Gly) | |
16 | g.89935708G>A | CA497194457 | TUBB3 | c.1257G>A (p.Val419=) n.4678G>A c.1041G>A (p.Val347=) c.277+2130G>A (n.277+2130G>A) c.*1342G>A (n.*1342G>A) c.2298G>A (p.Val766=) | gnomAD v4 |
16 | g.89935708G>C | CA497194459 | TUBB3 | c.1257G>C (p.Val419=) n.4678G>C c.1041G>C (p.Val347=) c.277+2130G>C (n.277+2130G>C) c.*1342G>C (n.*1342G>C) c.2298G>C (p.Val766=) | dbSNP |
16 | g.89935708G= | CA2242020777 | TUBB3 | c.1257G= (p.Val419=) n.4678G= c.1041G= (p.Val347=) c.277+2130G= (n.277+2130G=) c.*1342G= (n.*1342G=) c.2298G= (p.Val766=) | |
16 | g.89935708G>T | CA8256229 | TUBB3 | c.1257G>T (p.Val419=) n.4678G>T c.1041G>T (p.Val347=) c.277+2130G>T (n.277+2130G>T) c.*1342G>T (n.*1342G>T) c.2298G>T (p.Val766=) | ClinVar dbSNP ExAC gnomAD v4 |