Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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 |
16 | g.89935709T>A | CA397477087 | TUBB3 | c.1258T>A (p.Ser420Thr) n.4679T>A c.1042T>A (p.Ser348Thr) c.277+2131T>A (n.277+2131T>A) c.*1343T>A (n.*1343T>A) c.2299T>A (p.Ser767Thr) | |
16 | g.89935709T>C | CA397477088 | TUBB3 | c.1258T>C (p.Ser420Pro) n.4679T>C c.1042T>C (p.Ser348Pro) c.277+2131T>C (n.277+2131T>C) c.*1343T>C (n.*1343T>C) c.2299T>C (p.Ser767Pro) | |
16 | g.89935709T>G | CA397477089 | TUBB3 | c.1258T>G (p.Ser420Ala) n.4679T>G c.1042T>G (p.Ser348Ala) c.277+2131T>G (n.277+2131T>G) c.*1343T>G (n.*1343T>G) c.2299T>G (p.Ser767Ala) | |
16 | g.89935710C>A | CA397477090 | TUBB3 | c.1259C>A (p.Ser420Tyr) n.4680C>A c.1043C>A (p.Ser348Tyr) c.277+2132C>A (n.277+2132C>A) c.*1344C>A (n.*1344C>A) c.2300C>A (p.Ser767Tyr) | |
16 | g.89935710C= | CA2242020780 | TUBB3 | c.1259C= (p.Ser420=) n.4680C= c.1043C= (p.Ser348=) c.277+2132C= (n.277+2132C=) c.*1344C= (n.*1344C=) c.2300C= (p.Ser767=) | |
16 | g.89935710C>G | CA8256230 | TUBB3 | c.1259C>G (p.Ser420Cys) n.4680C>G c.1043C>G (p.Ser348Cys) c.277+2132C>G (n.277+2132C>G) c.*1344C>G (n.*1344C>G) c.2300C>G (p.Ser767Cys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.89935710C>T | CA397477091 | TUBB3 | c.1259C>T (p.Ser420Phe) n.4680C>T c.1043C>T (p.Ser348Phe) c.277+2132C>T (n.277+2132C>T) c.*1344C>T (n.*1344C>T) c.2300C>T (p.Ser767Phe) | |
16 | g.89935711C>A | CA497194461 | TUBB3 | c.1260C>A (p.Ser420=) n.4681C>A c.1044C>A (p.Ser348=) c.277+2133C>A (n.277+2133C>A) c.*1345C>A (n.*1345C>A) c.2301C>A (p.Ser767=) | |
16 | g.89935711C= | CA2242020784 | TUBB3 | c.1260C= (p.Ser420=) n.4681C= c.1044C= (p.Ser348=) c.277+2133C= (n.277+2133C=) c.*1345C= (n.*1345C=) c.2301C= (p.Ser767=) | |
16 | g.89935711C>G | CA497194462 | TUBB3 | c.1260C>G (p.Ser420=) n.4681C>G c.1044C>G (p.Ser348=) c.277+2133C>G (n.277+2133C>G) c.*1345C>G (n.*1345C>G) c.2301C>G (p.Ser767=) | gnomAD v4 |
16 | g.89935711C>T | CA8256231 | TUBB3 | c.1260C>T (p.Ser420=) n.4681C>T c.1044C>T (p.Ser348=) c.277+2133C>T (n.277+2133C>T) c.*1345C>T (n.*1345C>T) c.2301C>T (p.Ser767=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935711_89935712delinsCG | CA2242020783 | TUBB3 | c.1260_1261delinsCG (p.Ser420=) n.4681_4682delinsCG c.1044_1045delinsCG (p.Ser348=) c.277+2133_277+2134delinsCG (n.277+2133_277+2134delinsCG) c.*1345_*1346delinsCG (n.*1345_*1346delinsCG) c.2301_2302delinsCG (p.Ser767=) | |
16 | g.89935711_89935712delinsGA | CA286619370 | TUBB3 | c.1260_1261delinsGA (p.Glu421Lys) n.4681_4682delinsGA c.1044_1045delinsGA (p.Glu349Lys) c.277+2133_277+2134delinsGA (n.277+2133_277+2134delinsGA) c.*1345_*1346delinsGA (n.*1345_*1346delinsGA) c.2301_2302delinsGA (p.Glu768Lys) | dbSNP |
16 | g.89935712G>A | CA397477092 | TUBB3 | c.1261G>A (p.Glu421Lys) n.4682G>A c.1045G>A (p.Glu349Lys) c.277+2134G>A (n.277+2134G>A) c.*1346G>A (n.*1346G>A) c.2302G>A (p.Glu768Lys) | ClinVar dbSNP gnomAD v4 COSMIC |
16 | g.89935712G>C | CA397477093 | TUBB3 | c.1261G>C (p.Glu421Gln) n.4682G>C c.1045G>C (p.Glu349Gln) c.277+2134G>C (n.277+2134G>C) c.*1346G>C (n.*1346G>C) c.2302G>C (p.Glu768Gln) | |
16 | g.89935712G>T | CA397477094 | TUBB3 | c.1261G>T (p.Glu421Ter) n.4682G>T c.1045G>T (p.Glu349Ter) c.277+2134G>T (n.277+2134G>T) c.*1346G>T (n.*1346G>T) c.2302G>T (p.Glu768Ter) | |
16 | g.89935713A= | CA2242020785 | TUBB3 | c.1262A= (p.Glu421=) n.4683A= c.1046A= (p.Glu349=) c.277+2135A= (n.277+2135A=) c.*1347A= (n.*1347A=) c.2303A= (p.Glu768=) | |
16 | g.89935713A>C | CA397477096 | TUBB3 | c.1262A>C (p.Glu421Ala) n.4683A>C c.1046A>C (p.Glu349Ala) c.277+2135A>C (n.277+2135A>C) c.*1347A>C (n.*1347A>C) c.2303A>C (p.Glu768Ala) | dbSNP |
16 | g.89935713A>G | CA397477097 | TUBB3 | c.1262A>G (p.Glu421Gly) n.4683A>G c.1046A>G (p.Glu349Gly) c.277+2135A>G (n.277+2135A>G) c.*1347A>G (n.*1347A>G) c.2303A>G (p.Glu768Gly) | |
16 | g.89935713A>T | CA397477095 | TUBB3 | c.1262A>T (p.Glu421Val) n.4683A>T c.1046A>T (p.Glu349Val) c.277+2135A>T (n.277+2135A>T) c.*1347A>T (n.*1347A>T) c.2303A>T (p.Glu768Val) | |
16 | g.89935714G>A | CA497194466 | TUBB3 | c.1263G>A (p.Glu421=) n.4684G>A c.1047G>A (p.Glu349=) c.277+2136G>A (n.277+2136G>A) c.*1348G>A (n.*1348G>A) c.2304G>A (p.Glu768=) | |
16 | g.89935714G>C | CA397477098 | TUBB3 | c.1263G>C (p.Glu421Asp) n.4684G>C c.1047G>C (p.Glu349Asp) c.277+2136G>C (n.277+2136G>C) c.*1348G>C (n.*1348G>C) c.2304G>C (p.Glu768Asp) | |
16 | g.89935714G>T | CA397477099 | TUBB3 | c.1263G>T (p.Glu421Asp) n.4684G>T c.1047G>T (p.Glu349Asp) c.277+2136G>T (n.277+2136G>T) c.*1348G>T (n.*1348G>T) c.2304G>T (p.Glu768Asp) | |
16 | g.89935715T>A | CA397477100 | TUBB3 | c.1264T>A (p.Tyr422Asn) n.4685T>A c.1048T>A (p.Tyr350Asn) c.277+2137T>A (n.277+2137T>A) c.*1349T>A (n.*1349T>A) c.2305T>A (p.Tyr769Asn) | |
16 | g.89935715T>C | CA397477101 | TUBB3 | c.1264T>C (p.Tyr422His) n.4685T>C c.1048T>C (p.Tyr350His) c.277+2137T>C (n.277+2137T>C) c.*1349T>C (n.*1349T>C) c.2305T>C (p.Tyr769His) | |
16 | g.89935715T>G | CA397477102 | TUBB3 | c.1264T>G (p.Tyr422Asp) n.4685T>G c.1048T>G (p.Tyr350Asp) c.277+2137T>G (n.277+2137T>G) c.*1349T>G (n.*1349T>G) c.2305T>G (p.Tyr769Asp) | |
16 | g.89935716A>C | CA397477105 | TUBB3 | c.1265A>C (p.Tyr422Ser) n.4686A>C c.1049A>C (p.Tyr350Ser) c.277+2138A>C (n.277+2138A>C) c.*1350A>C (n.*1350A>C) c.2306A>C (p.Tyr769Ser) | |
16 | g.89935716A>G | CA397477103 | TUBB3 | c.1265A>G (p.Tyr422Cys) n.4686A>G c.1049A>G (p.Tyr350Cys) c.277+2138A>G (n.277+2138A>G) c.*1350A>G (n.*1350A>G) c.2306A>G (p.Tyr769Cys) | |
16 | g.89935716A>T | CA397477104 | TUBB3 | c.1265A>T (p.Tyr422Phe) n.4686A>T c.1049A>T (p.Tyr350Phe) c.277+2138A>T (n.277+2138A>T) c.*1350A>T (n.*1350A>T) c.2306A>T (p.Tyr769Phe) | |
16 | g.89935717C>A | CA397477106 | TUBB3 | c.1266C>A (p.Tyr422Ter) n.4687C>A c.1050C>A (p.Tyr350Ter) c.277+2139C>A (n.277+2139C>A) c.*1351C>A (n.*1351C>A) c.2307C>A (p.Tyr769Ter) | |
16 | g.89935717C>G | CA397477107 | TUBB3 | c.1266C>G (p.Tyr422Ter) n.4687C>G c.1050C>G (p.Tyr350Ter) c.277+2139C>G (n.277+2139C>G) c.*1351C>G (n.*1351C>G) c.2307C>G (p.Tyr769Ter) | |
16 | g.89935717C>T | CA497194471 | TUBB3 | c.1266C>T (p.Tyr422=) n.4687C>T c.1050C>T (p.Tyr350=) c.277+2139C>T (n.277+2139C>T) c.*1351C>T (n.*1351C>T) c.2307C>T (p.Tyr769=) | gnomAD v4 COSMIC |
16 | g.89935718C>A | CA397477108 | TUBB3 | c.1267C>A (p.Gln423Lys) n.4688C>A c.1051C>A (p.Gln351Lys) c.277+2140C>A (n.277+2140C>A) c.*1352C>A (n.*1352C>A) c.2308C>A (p.Gln770Lys) | |
16 | g.89935718C>G | CA397477109 | TUBB3 | c.1267C>G (p.Gln423Glu) n.4688C>G c.1051C>G (p.Gln351Glu) c.277+2140C>G (n.277+2140C>G) c.*1352C>G (n.*1352C>G) c.2308C>G (p.Gln770Glu) | |
16 | g.89935718C>T | CA397477110 | TUBB3 | c.1267C>T (p.Gln423Ter) n.4688C>T c.1051C>T (p.Gln351Ter) c.277+2140C>T (n.277+2140C>T) c.*1352C>T (n.*1352C>T) c.2308C>T (p.Gln770Ter) | ClinVar dbSNP gnomAD v4 COSMIC |
16 | g.89935719A>C | CA397477113 | TUBB3 | c.1268A>C (p.Gln423Pro) n.4689A>C c.1052A>C (p.Gln351Pro) c.277+2141A>C (n.277+2141A>C) c.*1353A>C (n.*1353A>C) c.2309A>C (p.Gln770Pro) | |
16 | g.89935719A>G | CA397477111 | TUBB3 | c.1268A>G (p.Gln423Arg) n.4689A>G c.1052A>G (p.Gln351Arg) c.277+2141A>G (n.277+2141A>G) c.*1353A>G (n.*1353A>G) c.2309A>G (p.Gln770Arg) | |
16 | g.89935719A>T | CA397477112 | TUBB3 | c.1268A>T (p.Gln423Leu) n.4689A>T c.1052A>T (p.Gln351Leu) c.277+2141A>T (n.277+2141A>T) c.*1353A>T (n.*1353A>T) c.2309A>T (p.Gln770Leu) | |
16 | g.89935720G>A | CA497194473 | TUBB3 | c.1269G>A (p.Gln423=) n.4690G>A c.1053G>A (p.Gln351=) c.277+2142G>A (n.277+2142G>A) c.*1354G>A (n.*1354G>A) c.2310G>A (p.Gln770=) | dbSNP gnomAD v4 |
16 | g.89935720G>C | CA397477114 | TUBB3 | c.1269G>C (p.Gln423His) n.4690G>C c.1053G>C (p.Gln351His) c.277+2142G>C (n.277+2142G>C) c.*1354G>C (n.*1354G>C) c.2310G>C (p.Gln770His) | |
16 | g.89935720G= | CA2242020786 | TUBB3 | c.1269G= (p.Gln423=) n.4690G= c.1053G= (p.Gln351=) c.277+2142G= (n.277+2142G=) c.*1354G= (n.*1354G=) c.2310G= (p.Gln770=) | |
16 | g.89935720G>T | CA397477115 | TUBB3 | c.1269G>T (p.Gln423His) n.4690G>T c.1053G>T (p.Gln351His) c.277+2142G>T (n.277+2142G>T) c.*1354G>T (n.*1354G>T) c.2310G>T (p.Gln770His) | |
16 | g.89935721C>A | CA397477116 | TUBB3 | c.1270C>A (p.Gln424Lys) n.4691C>A c.1054C>A (p.Gln352Lys) c.277+2143C>A (n.277+2143C>A) c.*1355C>A (n.*1355C>A) c.2311C>A (p.Gln771Lys) | |
16 | g.89935721C>G | CA397477117 | TUBB3 | c.1270C>G (p.Gln424Glu) n.4691C>G c.1054C>G (p.Gln352Glu) c.277+2143C>G (n.277+2143C>G) c.*1355C>G (n.*1355C>G) c.2311C>G (p.Gln771Glu) | |
16 | g.89935721C>T | CA397477118 | TUBB3 | c.1270C>T (p.Gln424Ter) n.4691C>T c.1054C>T (p.Gln352Ter) c.277+2143C>T (n.277+2143C>T) c.*1355C>T (n.*1355C>T) c.2311C>T (p.Gln771Ter) | |
16 | g.89935722A>C | CA397477119 | TUBB3 | c.1271A>C (p.Gln424Pro) n.4692A>C c.1055A>C (p.Gln352Pro) c.277+2144A>C (n.277+2144A>C) c.*1356A>C (n.*1356A>C) c.2312A>C (p.Gln771Pro) | ClinVar |
16 | g.89935722A>G | CA397477120 | TUBB3 | c.1271A>G (p.Gln424Arg) n.4692A>G c.1055A>G (p.Gln352Arg) c.277+2144A>G (n.277+2144A>G) c.*1356A>G (n.*1356A>G) c.2312A>G (p.Gln771Arg) | |
16 | g.89935722A>T | CA397477121 | TUBB3 | c.1271A>T (p.Gln424Leu) n.4692A>T c.1055A>T (p.Gln352Leu) c.277+2144A>T (n.277+2144A>T) c.*1356A>T (n.*1356A>T) c.2312A>T (p.Gln771Leu) | |
16 | g.89935723G>A | CA497194478 | TUBB3 | c.1272G>A (p.Gln424=) n.4693G>A c.1056G>A (p.Gln352=) c.277+2145G>A (n.277+2145G>A) c.*1357G>A (n.*1357G>A) c.2313G>A (p.Gln771=) | gnomAD v4 |
16 | g.89935723G>C | CA397477122 | TUBB3 | c.1272G>C (p.Gln424His) n.4693G>C c.1056G>C (p.Gln352His) c.277+2145G>C (n.277+2145G>C) c.*1357G>C (n.*1357G>C) c.2313G>C (p.Gln771His) | |
16 | g.89935723G>T | CA397477123 | TUBB3 | c.1272G>T (p.Gln424His) n.4693G>T c.1056G>T (p.Gln352His) c.277+2145G>T (n.277+2145G>T) c.*1357G>T (n.*1357G>T) c.2313G>T (p.Gln771His) | |
16 | g.89935724T>A | CA397477124 | TUBB3 | c.1273T>A (p.Tyr425Asn) n.4694T>A c.1057T>A (p.Tyr353Asn) c.277+2146T>A (n.277+2146T>A) c.*1358T>A (n.*1358T>A) c.2314T>A (p.Tyr772Asn) | |
16 | g.89935724T>C | CA397477125 | TUBB3 | c.1273T>C (p.Tyr425His) n.4694T>C c.1057T>C (p.Tyr353His) c.277+2146T>C (n.277+2146T>C) c.*1358T>C (n.*1358T>C) c.2314T>C (p.Tyr772His) | |
16 | g.89935724T>G | CA397477126 | TUBB3 | c.1273T>G (p.Tyr425Asp) n.4694T>G c.1057T>G (p.Tyr353Asp) c.277+2146T>G (n.277+2146T>G) c.*1358T>G (n.*1358T>G) c.2314T>G (p.Tyr772Asp) | |
16 | g.89935725A>C | CA397477127 | TUBB3 | c.1274A>C (p.Tyr425Ser) n.4695A>C c.1058A>C (p.Tyr353Ser) c.277+2147A>C (n.277+2147A>C) c.*1359A>C (n.*1359A>C) c.2315A>C (p.Tyr772Ser) | |
16 | g.89935725A>G | CA397477129 | TUBB3 | c.1274A>G (p.Tyr425Cys) n.4695A>G c.1058A>G (p.Tyr353Cys) c.277+2147A>G (n.277+2147A>G) c.*1359A>G (n.*1359A>G) c.2315A>G (p.Tyr772Cys) | |
16 | g.89935725A>T | CA397477128 | TUBB3 | c.1274A>T (p.Tyr425Phe) n.4695A>T c.1058A>T (p.Tyr353Phe) c.277+2147A>T (n.277+2147A>T) c.*1359A>T (n.*1359A>T) c.2315A>T (p.Tyr772Phe) | |
16 | g.89935726C>A | CA397477130 | TUBB3 | c.1275C>A (p.Tyr425Ter) n.4696C>A c.1059C>A (p.Tyr353Ter) c.277+2148C>A (n.277+2148C>A) c.*1360C>A (n.*1360C>A) c.2316C>A (p.Tyr772Ter) | |
16 | g.89935726C= | CA2242020788 | TUBB3 | c.1275C= (p.Tyr425=) n.4696C= c.1059C= (p.Tyr353=) c.277+2148C= (n.277+2148C=) c.*1360C= (n.*1360C=) c.2316C= (p.Tyr772=) | |
16 | g.89935726C>G | CA397477131 | TUBB3 | c.1275C>G (p.Tyr425Ter) n.4696C>G c.1059C>G (p.Tyr353Ter) c.277+2148C>G (n.277+2148C>G) c.*1360C>G (n.*1360C>G) c.2316C>G (p.Tyr772Ter) | |
16 | g.89935726C>T | CA497194482 | TUBB3 | c.1275C>T (p.Tyr425=) n.4696C>T c.1059C>T (p.Tyr353=) c.277+2148C>T (n.277+2148C>T) c.*1360C>T (n.*1360C>T) c.2316C>T (p.Tyr772=) | dbSNP gnomAD v4 COSMIC |
16 | g.89935727C>A | CA397477132 | TUBB3 | c.1276C>A (p.Gln426Lys) n.4697C>A c.1060C>A (p.Gln354Lys) c.277+2149C>A (n.277+2149C>A) c.*1361C>A (n.*1361C>A) c.2317C>A (p.Gln773Lys) | |
16 | g.89935727C= | CA2242020790 | TUBB3 | c.1276C= (p.Gln426=) n.4697C= c.1060C= (p.Gln354=) c.277+2149C= (n.277+2149C=) c.*1361C= (n.*1361C=) c.2317C= (p.Gln773=) | |
16 | g.89935727C>G | CA397477133 | TUBB3 | c.1276C>G (p.Gln426Glu) n.4697C>G c.1060C>G (p.Gln354Glu) c.277+2149C>G (n.277+2149C>G) c.*1361C>G (n.*1361C>G) c.2317C>G (p.Gln773Glu) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.89935727C>T | CA397477134 | TUBB3 | c.1276C>T (p.Gln426Ter) n.4697C>T c.1060C>T (p.Gln354Ter) c.277+2149C>T (n.277+2149C>T) c.*1361C>T (n.*1361C>T) c.2317C>T (p.Gln773Ter) | gnomAD v4 |
16 | g.89935728A>C | CA397477135 | TUBB3 | c.1277A>C (p.Gln426Pro) n.4698A>C c.1061A>C (p.Gln354Pro) c.277+2150A>C (n.277+2150A>C) c.*1362A>C (n.*1362A>C) c.2318A>C (p.Gln773Pro) | dbSNP |
16 | g.89935728A>G | CA397477136 | TUBB3 | c.1277A>G (p.Gln426Arg) n.4698A>G c.1061A>G (p.Gln354Arg) c.277+2150A>G (n.277+2150A>G) c.*1362A>G (n.*1362A>G) c.2318A>G (p.Gln773Arg) | |
16 | g.89935728A>T | CA397477137 | TUBB3 | c.1277A>T (p.Gln426Leu) n.4698A>T c.1061A>T (p.Gln354Leu) c.277+2150A>T (n.277+2150A>T) c.*1362A>T (n.*1362A>T) c.2318A>T (p.Gln773Leu) | |
16 | g.89935729G>A | CA497194484 | TUBB3 | c.1278G>A (p.Gln426=) n.4699G>A c.1062G>A (p.Gln354=) c.277+2151G>A (n.277+2151G>A) c.*1363G>A (n.*1363G>A) c.2319G>A (p.Gln773=) | |
16 | g.89935729G>C | CA397477138 | TUBB3 | c.1278G>C (p.Gln426His) n.4699G>C c.1062G>C (p.Gln354His) c.277+2151G>C (n.277+2151G>C) c.*1363G>C (n.*1363G>C) c.2319G>C (p.Gln773His) | |
16 | g.89935729G>T | CA397477139 | TUBB3 | c.1278G>T (p.Gln426His) n.4699G>T c.1062G>T (p.Gln354His) c.277+2151G>T (n.277+2151G>T) c.*1363G>T (n.*1363G>T) c.2319G>T (p.Gln773His) | |
16 | g.89935730G>A | CA397477140 | TUBB3 | c.1279G>A (p.Asp427Asn) n.4700G>A c.1063G>A (p.Asp355Asn) c.277+2152G>A (n.277+2152G>A) c.*1364G>A (n.*1364G>A) c.2320G>A (p.Asp774Asn) | gnomAD v4 |
16 | g.89935730G>C | CA397477141 | TUBB3 | c.1279G>C (p.Asp427His) n.4700G>C c.1063G>C (p.Asp355His) c.277+2152G>C (n.277+2152G>C) c.*1364G>C (n.*1364G>C) c.2320G>C (p.Asp774His) | |
16 | g.89935730G>T | CA397477142 | TUBB3 | c.1279G>T (p.Asp427Tyr) n.4700G>T c.1063G>T (p.Asp355Tyr) c.277+2152G>T (n.277+2152G>T) c.*1364G>T (n.*1364G>T) c.2320G>T (p.Asp774Tyr) | |
16 | g.89935731A>C | CA397477145 | TUBB3 | c.1280A>C (p.Asp427Ala) n.4701A>C c.1064A>C (p.Asp355Ala) c.277+2153A>C (n.277+2153A>C) c.*1365A>C (n.*1365A>C) c.2321A>C (p.Asp774Ala) | |
16 | g.89935731A>G | CA397477143 | TUBB3 | c.1280A>G (p.Asp427Gly) n.4701A>G c.1064A>G (p.Asp355Gly) c.277+2153A>G (n.277+2153A>G) c.*1365A>G (n.*1365A>G) c.2321A>G (p.Asp774Gly) | gnomAD v4 |
16 | g.89935731A>T | CA397477144 | TUBB3 | c.1280A>T (p.Asp427Val) n.4701A>T c.1064A>T (p.Asp355Val) c.277+2153A>T (n.277+2153A>T) c.*1365A>T (n.*1365A>T) c.2321A>T (p.Asp774Val) | |
16 | g.89935732C>A | CA397477146 | TUBB3 | c.1281C>A (p.Asp427Glu) n.4702C>A c.1065C>A (p.Asp355Glu) c.277+2154C>A (n.277+2154C>A) c.*1366C>A (n.*1366C>A) c.2322C>A (p.Asp774Glu) | |
16 | g.89935732C= | CA2242020791 | TUBB3 | c.1281C= (p.Asp427=) n.4702C= c.1065C= (p.Asp355=) c.277+2154C= (n.277+2154C=) c.*1366C= (n.*1366C=) c.2322C= (p.Asp774=) | |
16 | g.89935732C>G | CA397477147 | TUBB3 | c.1281C>G (p.Asp427Glu) n.4702C>G c.1065C>G (p.Asp355Glu) c.277+2154C>G (n.277+2154C>G) c.*1366C>G (n.*1366C>G) c.2322C>G (p.Asp774Glu) | gnomAD v4 |
16 | g.89935732C>T | CA8256232 | TUBB3 | c.1281C>T (p.Asp427=) n.4702C>T c.1065C>T (p.Asp355=) c.277+2154C>T (n.277+2154C>T) c.*1366C>T (n.*1366C>T) c.2322C>T (p.Asp774=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935733G>A | CA397477148 | TUBB3 | c.1282G>A (p.Ala428Thr) n.4703G>A c.1066G>A (p.Ala356Thr) c.277+2155G>A (n.277+2155G>A) c.*1367G>A (n.*1367G>A) c.2323G>A (p.Ala775Thr) | gnomAD v4 COSMIC |
16 | g.89935733G>C | CA397477149 | TUBB3 | c.1282G>C (p.Ala428Pro) n.4703G>C c.1066G>C (p.Ala356Pro) c.277+2155G>C (n.277+2155G>C) c.*1367G>C (n.*1367G>C) c.2323G>C (p.Ala775Pro) | |
16 | g.89935733G>T | CA397477150 | TUBB3 | c.1282G>T (p.Ala428Ser) n.4703G>T c.1066G>T (p.Ala356Ser) c.277+2155G>T (n.277+2155G>T) c.*1367G>T (n.*1367G>T) c.2323G>T (p.Ala775Ser) | gnomAD v4 |
16 | g.89935734C>A | CA397477151 | TUBB3 | c.1283C>A (p.Ala428Asp) n.4704C>A c.1067C>A (p.Ala356Asp) c.277+2156C>A (n.277+2156C>A) c.*1368C>A (n.*1368C>A) c.2324C>A (p.Ala775Asp) | |
16 | g.89935734C= | CA2242020792 | TUBB3 | c.1283C= (p.Ala428=) n.4704C= c.1067C= (p.Ala356=) c.277+2156C= (n.277+2156C=) c.*1368C= (n.*1368C=) c.2324C= (p.Ala775=) | |
16 | g.89935734C>G | CA397477152 | TUBB3 | c.1283C>G (p.Ala428Gly) n.4704C>G c.1067C>G (p.Ala356Gly) c.277+2156C>G (n.277+2156C>G) c.*1368C>G (n.*1368C>G) c.2324C>G (p.Ala775Gly) | |
16 | g.89935734C>T | CA397477153 | TUBB3 | c.1283C>T (p.Ala428Val) n.4704C>T c.1067C>T (p.Ala356Val) c.277+2156C>T (n.277+2156C>T) c.*1368C>T (n.*1368C>T) c.2324C>T (p.Ala775Val) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.89935735C>A | CA497194490 | TUBB3 | c.1284C>A (p.Ala428=) n.4705C>A c.1068C>A (p.Ala356=) c.277+2157C>A (n.277+2157C>A) c.*1369C>A (n.*1369C>A) c.2325C>A (p.Ala775=) | |
16 | g.89935735C>G | CA497194491 | TUBB3 | c.1284C>G (p.Ala428=) n.4705C>G c.1068C>G (p.Ala356=) c.277+2157C>G (n.277+2157C>G) c.*1369C>G (n.*1369C>G) c.2325C>G (p.Ala775=) | |
16 | g.89935735C>T | CA497194492 | TUBB3 | c.1284C>T (p.Ala428=) n.4705C>T c.1068C>T (p.Ala356=) c.277+2157C>T (n.277+2157C>T) c.*1369C>T (n.*1369C>T) c.2325C>T (p.Ala775=) | gnomAD v4 COSMIC |
16 | g.89935736A>C | CA397477154 | TUBB3 | c.1285A>C (p.Thr429Pro) n.4706A>C c.1069A>C (p.Thr357Pro) c.277+2158A>C (n.277+2158A>C) c.*1370A>C (n.*1370A>C) c.2326A>C (p.Thr776Pro) | |
16 | g.89935736A>G | CA397477155 | TUBB3 | c.1285A>G (p.Thr429Ala) n.4706A>G c.1069A>G (p.Thr357Ala) c.277+2158A>G (n.277+2158A>G) c.*1370A>G (n.*1370A>G) c.2326A>G (p.Thr776Ala) | |
16 | g.89935736A>T | CA397477156 | TUBB3 | c.1285A>T (p.Thr429Ser) n.4706A>T c.1069A>T (p.Thr357Ser) c.277+2158A>T (n.277+2158A>T) c.*1370A>T (n.*1370A>T) c.2326A>T (p.Thr776Ser) | |
16 | g.89935737C>A | CA397477157 | TUBB3 | c.1286C>A (p.Thr429Lys) n.4707C>A c.1070C>A (p.Thr357Lys) c.277+2159C>A (n.277+2159C>A) c.*1371C>A (n.*1371C>A) c.2327C>A (p.Thr776Lys) | |
16 | g.89935737C= | CA2242020796 | TUBB3 | c.1286C= (p.Thr429=) n.4707C= c.1070C= (p.Thr357=) c.277+2159C= (n.277+2159C=) c.*1371C= (n.*1371C=) c.2327C= (p.Thr776=) | |
16 | g.89935737C>G | CA397477158 | TUBB3 | c.1286C>G (p.Thr429Arg) n.4707C>G c.1070C>G (p.Thr357Arg) c.277+2159C>G (n.277+2159C>G) c.*1371C>G (n.*1371C>G) c.2327C>G (p.Thr776Arg) | |
16 | g.89935737C>T | CA8256233 | TUBB3 | c.1286C>T (p.Thr429Met) n.4707C>T c.1070C>T (p.Thr357Met) c.277+2159C>T (n.277+2159C>T) c.*1371C>T (n.*1371C>T) c.2327C>T (p.Thr776Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935738G>A | CA209122 | TUBB3 | c.1287G>A (p.Thr429=) n.4708G>A c.1071G>A (p.Thr357=) c.277+2160G>A (n.277+2160G>A) c.*1372G>A (n.*1372G>A) c.2328G>A (p.Thr776=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935738G>C | CA497194497 | TUBB3 | c.1287G>C (p.Thr429=) n.4708G>C c.1071G>C (p.Thr357=) c.277+2160G>C (n.277+2160G>C) c.*1372G>C (n.*1372G>C) c.2328G>C (p.Thr776=) | |
16 | g.89935738G= | CA2242020806 | TUBB3 | c.1287G= (p.Thr429=) n.4708G= c.1071G= (p.Thr357=) c.277+2160G= (n.277+2160G=) c.*1372G= (n.*1372G=) c.2328G= (p.Thr776=) | |
16 | g.89935738G>T | CA8256234 | TUBB3 | c.1287G>T (p.Thr429=) n.4708G>T c.1071G>T (p.Thr357=) c.277+2160G>T (n.277+2160G>T) c.*1372G>T (n.*1372G>T) c.2328G>T (p.Thr776=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.89935739G>A | CA397477159 | TUBB3 | c.1288G>A (p.Ala430Thr) n.4709G>A c.1072G>A (p.Ala358Thr) c.277+2161G>A (n.277+2161G>A) c.*1373G>A (n.*1373G>A) c.2329G>A (p.Ala777Thr) | |
16 | g.89935739G>C | CA350350 | TUBB3 | c.1288G>C (p.Ala430Pro) n.4709G>C c.1072G>C (p.Ala358Pro) c.277+2161G>C (n.277+2161G>C) c.*1373G>C (n.*1373G>C) c.2329G>C (p.Ala777Pro) | ClinVar dbSNP COSMIC |
16 | g.89935739G= | CA2242020810 | TUBB3 | c.1288G= (p.Ala430=) n.4709G= c.1072G= (p.Ala358=) c.277+2161G= (n.277+2161G=) c.*1373G= (n.*1373G=) c.2329G= (p.Ala777=) | |
16 | g.89935739G>T | CA397477160 | TUBB3 | c.1288G>T (p.Ala430Ser) n.4709G>T c.1072G>T (p.Ala358Ser) c.277+2161G>T (n.277+2161G>T) c.*1373G>T (n.*1373G>T) c.2329G>T (p.Ala777Ser) | |
16 | g.89935740C>A | CA397477161 | TUBB3 | c.1289C>A (p.Ala430Asp) n.4710C>A c.1073C>A (p.Ala358Asp) c.277+2162C>A (n.277+2162C>A) c.*1374C>A (n.*1374C>A) c.2330C>A (p.Ala777Asp) | |
16 | g.89935740C>G | CA397477162 | TUBB3 | c.1289C>G (p.Ala430Gly) n.4710C>G c.1073C>G (p.Ala358Gly) c.277+2162C>G (n.277+2162C>G) c.*1374C>G (n.*1374C>G) c.2330C>G (p.Ala777Gly) | |
16 | g.89935740C>T | CA397477163 | TUBB3 | c.1289C>T (p.Ala430Val) n.4710C>T c.1073C>T (p.Ala358Val) c.277+2162C>T (n.277+2162C>T) c.*1374C>T (n.*1374C>T) c.2330C>T (p.Ala777Val) | |
16 | g.89935741C>A | CA497194502 | TUBB3 | c.1290C>A (p.Ala430=) n.4711C>A c.1074C>A (p.Ala358=) c.277+2163C>A (n.277+2163C>A) c.*1375C>A (n.*1375C>A) c.2331C>A (p.Ala777=) | |
16 | g.89935741C= | CA2242020812 | TUBB3 | c.1290C= (p.Ala430=) n.4711C= c.1074C= (p.Ala358=) c.277+2163C= (n.277+2163C=) c.*1375C= (n.*1375C=) c.2331C= (p.Ala777=) | |
16 | g.89935741C>G | CA497194504 | TUBB3 | c.1290C>G (p.Ala430=) n.4711C>G c.1074C>G (p.Ala358=) c.277+2163C>G (n.277+2163C>G) c.*1375C>G (n.*1375C>G) c.2331C>G (p.Ala777=) | |
16 | g.89935741C>T | CA8256235 | TUBB3 | c.1290C>T (p.Ala430=) n.4711C>T c.1074C>T (p.Ala358=) c.277+2163C>T (n.277+2163C>T) c.*1375C>T (n.*1375C>T) c.2331C>T (p.Ala777=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935742G>A | CA286619400 | TUBB3 | c.1291G>A (p.Glu431Lys) n.4712G>A c.1075G>A (p.Glu359Lys) c.277+2164G>A (n.277+2164G>A) c.*1376G>A (n.*1376G>A) c.2332G>A (p.Glu778Lys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
16 | g.89935742G>C | CA397477164 | TUBB3 | c.1291G>C (p.Glu431Gln) n.4712G>C c.1075G>C (p.Glu359Gln) c.277+2164G>C (n.277+2164G>C) c.*1376G>C (n.*1376G>C) c.2332G>C (p.Glu778Gln) | |
16 | g.89935742G= | CA2242020815 | TUBB3 | c.1291G= (p.Glu431=) n.4712G= c.1075G= (p.Glu359=) c.277+2164G= (n.277+2164G=) c.*1376G= (n.*1376G=) c.2332G= (p.Glu778=) | |
16 | g.89935742G>T | CA397477165 | TUBB3 | c.1291G>T (p.Glu431Ter) n.4712G>T c.1075G>T (p.Glu359Ter) c.277+2164G>T (n.277+2164G>T) c.*1376G>T (n.*1376G>T) c.2332G>T (p.Glu778Ter) | ClinVar gnomAD v4 |
16 | g.89935743A>C | CA397477168 | TUBB3 | c.1292A>C (p.Glu431Ala) n.4713A>C c.1076A>C (p.Glu359Ala) c.277+2165A>C (n.277+2165A>C) c.*1377A>C (n.*1377A>C) c.2333A>C (p.Glu778Ala) | |
16 | g.89935743A>G | CA397477167 | TUBB3 | c.1292A>G (p.Glu431Gly) n.4713A>G c.1076A>G (p.Glu359Gly) c.277+2165A>G (n.277+2165A>G) c.*1377A>G (n.*1377A>G) c.2333A>G (p.Glu778Gly) | |
16 | g.89935743A>T | CA397477166 | TUBB3 | c.1292A>T (p.Glu431Val) n.4713A>T c.1076A>T (p.Glu359Val) c.277+2165A>T (n.277+2165A>T) c.*1377A>T (n.*1377A>T) c.2333A>T (p.Glu778Val) | |
16 | g.89935744G>A | CA497194507 | TUBB3 | c.1293G>A (p.Glu431=) n.4714G>A c.1077G>A (p.Glu359=) c.277+2166G>A (n.277+2166G>A) c.*1378G>A (n.*1378G>A) c.2334G>A (p.Glu778=) | |
16 | g.89935744G>C | CA397477169 | TUBB3 | c.1293G>C (p.Glu431Asp) n.4714G>C c.1077G>C (p.Glu359Asp) c.277+2166G>C (n.277+2166G>C) c.*1378G>C (n.*1378G>C) c.2334G>C (p.Glu778Asp) | |
16 | g.89935744G>T | CA397477170 | TUBB3 | c.1293G>T (p.Glu431Asp) n.4714G>T c.1077G>T (p.Glu359Asp) c.277+2166G>T (n.277+2166G>T) c.*1378G>T (n.*1378G>T) c.2334G>T (p.Glu778Asp) | COSMIC |
16 | g.89935745G>A | CA397477171 | TUBB3 | c.1294G>A (p.Glu432Lys) n.4715G>A c.1078G>A (p.Glu360Lys) c.277+2167G>A (n.277+2167G>A) c.*1379G>A (n.*1379G>A) c.2335G>A (p.Glu779Lys) | |
16 | g.89935745G>C | CA397477172 | TUBB3 | c.1294G>C (p.Glu432Gln) n.4715G>C c.1078G>C (p.Glu360Gln) c.277+2167G>C (n.277+2167G>C) c.*1379G>C (n.*1379G>C) c.2335G>C (p.Glu779Gln) | |
16 | g.89935745G>T | CA397477173 | TUBB3 | c.1294G>T (p.Glu432Ter) n.4715G>T c.1078G>T (p.Glu360Ter) c.277+2167G>T (n.277+2167G>T) c.*1379G>T (n.*1379G>T) c.2335G>T (p.Glu779Ter) | |
16 | g.89935747_89935749dup | CA2635070901 | TUBB3 | c.1296_1298dup (p.Glu433_Gly434insGlu) n.4717_4719dup c.1080_1082dup (p.Glu361_Gly362insGlu) c.277+2169_277+2171dup (n.277+2169_277+2171dup) c.*1381_*1383dup (n.*1381_*1383dup) c.2337_2339dup (p.Glu780_Gly781insGlu) | gnomAD v4 |
16 | g.89935746A>C | CA397477174 | TUBB3 | c.1295A>C (p.Glu432Ala) n.4716A>C c.1079A>C (p.Glu360Ala) c.277+2168A>C (n.277+2168A>C) c.*1380A>C (n.*1380A>C) c.2336A>C (p.Glu779Ala) | |
16 | g.89935746A>G | CA397477175 | TUBB3 | c.1295A>G (p.Glu432Gly) n.4716A>G c.1079A>G (p.Glu360Gly) c.277+2168A>G (n.277+2168A>G) c.*1380A>G (n.*1380A>G) c.2336A>G (p.Glu779Gly) | gnomAD v4 |
16 | g.89935746A>T | CA397477176 | TUBB3 | c.1295A>T (p.Glu432Val) n.4716A>T c.1079A>T (p.Glu360Val) c.277+2168A>T (n.277+2168A>T) c.*1380A>T (n.*1380A>T) c.2336A>T (p.Glu779Val) | |
16 | g.89935747A= | CA2242020816 | TUBB3 | c.1296A= (p.Glu432=) n.4717A= c.1080A= (p.Glu360=) c.277+2169A= (n.277+2169A=) c.*1381A= (n.*1381A=) c.2337A= (p.Glu779=) | |
16 | g.89935747A>C | CA397477177 | TUBB3 | c.1296A>C (p.Glu432Asp) n.4717A>C c.1080A>C (p.Glu360Asp) c.277+2169A>C (n.277+2169A>C) c.*1381A>C (n.*1381A>C) c.2337A>C (p.Glu779Asp) | |
16 | g.89935747A>G | CA497194512 | TUBB3 | c.1296A>G (p.Glu432=) n.4717A>G c.1080A>G (p.Glu360=) c.277+2169A>G (n.277+2169A>G) c.*1381A>G (n.*1381A>G) c.2337A>G (p.Glu779=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935747A>T | CA397477178 | TUBB3 | c.1296A>T (p.Glu432Asp) n.4717A>T c.1080A>T (p.Glu360Asp) c.277+2169A>T (n.277+2169A>T) c.*1381A>T (n.*1381A>T) c.2337A>T (p.Glu779Asp) | |
16 | g.89935748G>A | CA397477179 | TUBB3 | c.1297G>A (p.Glu433Lys) n.4718G>A c.1081G>A (p.Glu361Lys) c.277+2170G>A (n.277+2170G>A) c.*1382G>A (n.*1382G>A) c.2338G>A (p.Glu780Lys) | |
16 | g.89935748G>C | CA397477180 | TUBB3 | c.1297G>C (p.Glu433Gln) n.4718G>C c.1081G>C (p.Glu361Gln) c.277+2170G>C (n.277+2170G>C) c.*1382G>C (n.*1382G>C) c.2338G>C (p.Glu780Gln) | |
16 | g.89935748G>T | CA397477181 | TUBB3 | c.1297G>T (p.Glu433Ter) n.4718G>T c.1081G>T (p.Glu361Ter) c.277+2170G>T (n.277+2170G>T) c.*1382G>T (n.*1382G>T) c.2338G>T (p.Glu780Ter) | gnomAD v4 |
16 | g.89935749A>C | CA397477184 | TUBB3 | c.1298A>C (p.Glu433Ala) n.4719A>C c.1082A>C (p.Glu361Ala) c.277+2171A>C (n.277+2171A>C) c.*1383A>C (n.*1383A>C) c.2339A>C (p.Glu780Ala) | gnomAD v4 |
16 | g.89935749A>G | CA397477183 | TUBB3 | c.1298A>G (p.Glu433Gly) n.4719A>G c.1082A>G (p.Glu361Gly) c.277+2171A>G (n.277+2171A>G) c.*1383A>G (n.*1383A>G) c.2339A>G (p.Glu780Gly) | gnomAD v4 |
16 | g.89935749A>T | CA397477182 | TUBB3 | c.1298A>T (p.Glu433Val) n.4719A>T c.1082A>T (p.Glu361Val) c.277+2171A>T (n.277+2171A>T) c.*1383A>T (n.*1383A>T) c.2339A>T (p.Glu780Val) | |
16 | g.89935750G>A | CA8256236 | TUBB3 | c.1299G>A (p.Glu433=) n.4720G>A c.1083G>A (p.Glu361=) c.277+2172G>A (n.277+2172G>A) c.*1384G>A (n.*1384G>A) c.2340G>A (p.Glu780=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.89935750G>C | CA397477185 | TUBB3 | c.1299G>C (p.Glu433Asp) n.4720G>C c.1083G>C (p.Glu361Asp) c.277+2172G>C (n.277+2172G>C) c.*1384G>C (n.*1384G>C) c.2340G>C (p.Glu780Asp) | |
16 | g.89935750G= | CA2242020818 | TUBB3 | c.1299G= (p.Glu433=) n.4720G= c.1083G= (p.Glu361=) c.277+2172G= (n.277+2172G=) c.*1384G= (n.*1384G=) c.2340G= (p.Glu780=) | |
16 | g.89935750G>T | CA397477186 | TUBB3 | c.1299G>T (p.Glu433Asp) n.4720G>T c.1083G>T (p.Glu361Asp) c.277+2172G>T (n.277+2172G>T) c.*1384G>T (n.*1384G>T) c.2340G>T (p.Glu780Asp) | |
16 | g.89935751G>A | CA397477187 | TUBB3 | c.1300G>A (p.Gly434Ser) n.4721G>A c.1084G>A (p.Gly362Ser) c.277+2173G>A (n.277+2173G>A) c.*1385G>A (n.*1385G>A) c.2341G>A (p.Gly781Ser) | gnomAD v4 |
16 | g.89935751G>C | CA397477188 | TUBB3 | c.1300G>C (p.Gly434Arg) n.4721G>C c.1084G>C (p.Gly362Arg) c.277+2173G>C (n.277+2173G>C) c.*1385G>C (n.*1385G>C) c.2341G>C (p.Gly781Arg) | |
16 | g.89935751G>T | CA397477189 | TUBB3 | c.1300G>T (p.Gly434Cys) n.4721G>T c.1084G>T (p.Gly362Cys) c.277+2173G>T (n.277+2173G>T) c.*1385G>T (n.*1385G>T) c.2341G>T (p.Gly781Cys) | |
16 | g.89935752G>A | CA397477190 | TUBB3 | c.1301G>A (p.Gly434Asp) n.4722G>A c.1085G>A (p.Gly362Asp) c.277+2174G>A (n.277+2174G>A) c.*1386G>A (n.*1386G>A) c.2342G>A (p.Gly781Asp) | |
16 | g.89935752G>C | CA397477191 | TUBB3 | c.1301G>C (p.Gly434Ala) n.4722G>C c.1085G>C (p.Gly362Ala) c.277+2174G>C (n.277+2174G>C) c.*1386G>C (n.*1386G>C) c.2342G>C (p.Gly781Ala) | |
16 | g.89935752G= | CA2242020820 | TUBB3 | c.1301G= (p.Gly434=) n.4722G= c.1085G= (p.Gly362=) c.277+2174G= (n.277+2174G=) c.*1386G= (n.*1386G=) c.2342G= (p.Gly781=) | |
16 | g.89935752G>T | CA397477192 | TUBB3 | c.1301G>T (p.Gly434Val) n.4722G>T c.1085G>T (p.Gly362Val) c.277+2174G>T (n.277+2174G>T) c.*1386G>T (n.*1386G>T) c.2342G>T (p.Gly781Val) | dbSNP |
16 | g.89935753C>A | CA497194519 | TUBB3 | c.1302C>A (p.Gly434=) n.4723C>A c.1086C>A (p.Gly362=) c.277+2175C>A (n.277+2175C>A) c.*1387C>A (n.*1387C>A) c.2343C>A (p.Gly781=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935753C= | CA2242020824 | TUBB3 | c.1302C= (p.Gly434=) n.4723C= c.1086C= (p.Gly362=) c.277+2175C= (n.277+2175C=) c.*1387C= (n.*1387C=) c.2343C= (p.Gly781=) | |
16 | g.89935753C>G | CA497194520 | TUBB3 | c.1302C>G (p.Gly434=) n.4723C>G c.1086C>G (p.Gly362=) c.277+2175C>G (n.277+2175C>G) c.*1387C>G (n.*1387C>G) c.2343C>G (p.Gly781=) | gnomAD v4 |
16 | g.89935753C>T | CA8256237 | TUBB3 | c.1302C>T (p.Gly434=) n.4723C>T c.1086C>T (p.Gly362=) c.277+2175C>T (n.277+2175C>T) c.*1387C>T (n.*1387C>T) c.2343C>T (p.Gly781=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935754G>A | CA8256238 | TUBB3 | c.1303G>A (p.Glu435Lys) n.4724G>A c.1087G>A (p.Glu363Lys) c.277+2176G>A (n.277+2176G>A) c.*1388G>A (n.*1388G>A) c.2344G>A (p.Glu782Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935754G>C | CA397477193 | TUBB3 | c.1303G>C (p.Glu435Gln) n.4724G>C c.1087G>C (p.Glu363Gln) c.277+2176G>C (n.277+2176G>C) c.*1388G>C (n.*1388G>C) c.2344G>C (p.Glu782Gln) | |
16 | g.89935754G= | CA2242020827 | TUBB3 | c.1303G= (p.Glu435=) n.4724G= c.1087G= (p.Glu363=) c.277+2176G= (n.277+2176G=) c.*1388G= (n.*1388G=) c.2344G= (p.Glu782=) | |
16 | g.89935754G>T | CA397477194 | TUBB3 | c.1303G>T (p.Glu435Ter) n.4724G>T c.1087G>T (p.Glu363Ter) c.277+2176G>T (n.277+2176G>T) c.*1388G>T (n.*1388G>T) c.2344G>T (p.Glu782Ter) | |
16 | g.89935755A>C | CA397477196 | TUBB3 | c.1304A>C (p.Glu435Ala) n.4725A>C c.1088A>C (p.Glu363Ala) c.277+2177A>C (n.277+2177A>C) c.*1389A>C (n.*1389A>C) c.2345A>C (p.Glu782Ala) | |
16 | g.89935755A>G | CA397477197 | TUBB3 | c.1304A>G (p.Glu435Gly) n.4725A>G c.1088A>G (p.Glu363Gly) c.277+2177A>G (n.277+2177A>G) c.*1389A>G (n.*1389A>G) c.2345A>G (p.Glu782Gly) | |
16 | g.89935755A>T | CA397477195 | TUBB3 | c.1304A>T (p.Glu435Val) n.4725A>T c.1088A>T (p.Glu363Val) c.277+2177A>T (n.277+2177A>T) c.*1389A>T (n.*1389A>T) c.2345A>T (p.Glu782Val) | |
16 | g.89935756G>A | CA497194526 | TUBB3 | c.1305G>A (p.Glu435=) n.4726G>A c.1089G>A (p.Glu363=) c.277+2178G>A (n.277+2178G>A) c.*1390G>A (n.*1390G>A) c.2346G>A (p.Glu782=) | |
16 | g.89935756G>C | CA397477198 | TUBB3 | c.1305G>C (p.Glu435Asp) n.4726G>C c.1089G>C (p.Glu363Asp) c.277+2178G>C (n.277+2178G>C) c.*1390G>C (n.*1390G>C) c.2346G>C (p.Glu782Asp) | |
16 | g.89935756G>T | CA397477199 | TUBB3 | c.1305G>T (p.Glu435Asp) n.4726G>T c.1089G>T (p.Glu363Asp) c.277+2178G>T (n.277+2178G>T) c.*1390G>T (n.*1390G>T) c.2346G>T (p.Glu782Asp) | |
16 | g.89935757A= | CA2242020831 | TUBB3 | c.1306A= (p.Met436=) n.4727A= c.1090A= (p.Met364=) c.277+2179A= (n.277+2179A=) c.*1391A= (n.*1391A=) c.2347A= (p.Met783=) | |
16 | g.89935757A>C | CA397477200 | TUBB3 | c.1306A>C (p.Met436Leu) n.4727A>C c.1090A>C (p.Met364Leu) c.277+2179A>C (n.277+2179A>C) c.*1391A>C (n.*1391A>C) c.2347A>C (p.Met783Leu) | |
16 | g.89935757A>G | CA397477201 | TUBB3 | c.1306A>G (p.Met436Val) n.4727A>G c.1090A>G (p.Met364Val) c.277+2179A>G (n.277+2179A>G) c.*1391A>G (n.*1391A>G) c.2347A>G (p.Met783Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935757A>T | CA397477202 | TUBB3 | c.1306A>T (p.Met436Leu) n.4727A>T c.1090A>T (p.Met364Leu) c.277+2179A>T (n.277+2179A>T) c.*1391A>T (n.*1391A>T) c.2347A>T (p.Met783Leu) | |
16 | g.89935758T>A | CA397477204 | TUBB3 | c.1307T>A (p.Met436Lys) n.4728T>A c.1091T>A (p.Met364Lys) c.277+2180T>A (n.277+2180T>A) c.*1392T>A (n.*1392T>A) c.2348T>A (p.Met783Lys) | |
16 | g.89935758T>C | CA397477203 | TUBB3 | c.1307T>C (p.Met436Thr) n.4728T>C c.1091T>C (p.Met364Thr) c.277+2180T>C (n.277+2180T>C) c.*1392T>C (n.*1392T>C) c.2348T>C (p.Met783Thr) | ClinVar dbSNP |
16 | g.89935758T>G | CA8256239 | TUBB3 | c.1307T>G (p.Met436Arg) n.4728T>G c.1091T>G (p.Met364Arg) c.277+2180T>G (n.277+2180T>G) c.*1392T>G (n.*1392T>G) c.2348T>G (p.Met783Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.89935758T= | CA2242020835 | TUBB3 | c.1307T= (p.Met436=) n.4728T= c.1091T= (p.Met364=) c.277+2180T= (n.277+2180T=) c.*1392T= (n.*1392T=) c.2348T= (p.Met783=) | |
16 | g.89935759G>A | CA397477205 | TUBB3 | c.1308G>A (p.Met436Ile) n.4729G>A c.1092G>A (p.Met364Ile) c.277+2181G>A (n.277+2181G>A) c.*1393G>A (n.*1393G>A) c.2349G>A (p.Met783Ile) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.89935759G>C | CA397477206 | TUBB3 | c.1308G>C (p.Met436Ile) n.4729G>C c.1092G>C (p.Met364Ile) c.277+2181G>C (n.277+2181G>C) c.*1393G>C (n.*1393G>C) c.2349G>C (p.Met783Ile) | |
16 | g.89935759G= | CA2242020839 | TUBB3 | c.1308G= (p.Met436=) n.4729G= c.1092G= (p.Met364=) c.277+2181G= (n.277+2181G=) c.*1393G= (n.*1393G=) c.2349G= (p.Met783=) | |
16 | g.89935759G>T | CA397477207 | TUBB3 | c.1308G>T (p.Met436Ile) n.4729G>T c.1092G>T (p.Met364Ile) c.277+2181G>T (n.277+2181G>T) c.*1393G>T (n.*1393G>T) c.2349G>T (p.Met783Ile) |