Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.89935646A=CA2242020692TUBB3c.1195A= (p.Thr399=)
n.4616A=
c.979A= (p.Thr327=)
c.277+2068A= (n.277+2068A=)
c.*1280A= (n.*1280A=)
c.2236A= (p.Thr746=)
16g.89935646A>CCA397476936TUBB3c.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)
16g.89935646A>GCA397476938TUBB3c.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)
16g.89935646A>TCA397476937TUBB3c.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
16g.89935647C>ACA397476939TUBB3c.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)
16g.89935647C=CA2242020696TUBB3c.1196C= (p.Thr399=)
n.4617C=
c.980C= (p.Thr327=)
c.277+2069C= (n.277+2069C=)
c.*1281C= (n.*1281C=)
c.2237C= (p.Thr746=)
16g.89935647C>GCA397476940TUBB3c.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
16g.89935647C>TCA286619350TUBB3c.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
16g.89935648G>ACA8256218TUBB3c.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
16g.89935648G>CCA8256219TUBB3c.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
16g.89935648G=CA2242020700TUBB3c.1197G= (p.Thr399=)
n.4618G=
c.981G= (p.Thr327=)
c.277+2070G= (n.277+2070G=)
c.*1282G= (n.*1282G=)
c.2238G= (p.Thr746=)
16g.89935648G>TCA497194433TUBB3c.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=)
16g.89935649G>ACA397476941TUBB3c.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
16g.89935649G>CCA397476943TUBB3c.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)
16g.89935649G>TCA397476942TUBB3c.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)
16g.89935650G>ACA397476944TUBB3c.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)
16g.89935650G>CCA397476945TUBB3c.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)
16g.89935650G>TCA397476946TUBB3c.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)
16g.89935651C>ACA497194434TUBB3c.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
16g.89935651C=CA2242020706TUBB3c.1200C= (p.Gly400=)
n.4621C=
c.984C= (p.Gly328=)
c.277+2073C= (n.277+2073C=)
c.*1285C= (n.*1285C=)
c.2241C= (p.Gly747=)
16g.89935651C>GCA497194435TUBB3c.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=)
16g.89935651C>TCA8256220TUBB3c.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
16g.89935652G>ACA397476947TUBB3c.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
16g.89935652G>CCA397476948TUBB3c.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)
16g.89935652G=CA2242020712TUBB3c.1201G= (p.Glu401=)
n.4622G=
c.985G= (p.Glu329=)
c.277+2074G= (n.277+2074G=)
c.*1286G= (n.*1286G=)
c.2242G= (p.Glu748=)
16g.89935652G>TCA397476949TUBB3c.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)
16g.89935653A>CCA397476950TUBB3c.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)
16g.89935653A>GCA397476951TUBB3c.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)
16g.89935653A>TCA397476952TUBB3c.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)
16g.89935654G>ACA497194436TUBB3c.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
16g.89935654G>CCA397476953TUBB3c.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)
16g.89935654G=CA2242020716TUBB3c.1203G= (p.Glu401=)
n.4624G=
c.987G= (p.Glu329=)
c.277+2076G= (n.277+2076G=)
c.*1288G= (n.*1288G=)
c.2244G= (p.Glu748=)
16g.89935654G>TCA397476954TUBB3c.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)
16g.89935655G>ACA397476955TUBB3c.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)
16g.89935655G>CCA397476957TUBB3c.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)
16g.89935655G>TCA397476956TUBB3c.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)
16g.89935656G>ACA397476958TUBB3c.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)
16g.89935656G>CCA397476959TUBB3c.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)
16g.89935656G>TCA397476960TUBB3c.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)
16g.89935657C>ACA497194437TUBB3c.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=)
16g.89935657C=CA2242020720TUBB3c.1206C= (p.Gly402=)
n.4627C=
c.990C= (p.Gly330=)
c.277+2079C= (n.277+2079C=)
c.*1291C= (n.*1291C=)
c.2247C= (p.Gly749=)
16g.89935657C>GCA497194438TUBB3c.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
16g.89935657C>TCA8256221TUBB3c.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
16g.89935658A>CCA397476961TUBB3c.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)
16g.89935658A>GCA397476962TUBB3c.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)
16g.89935658A>TCA397476963TUBB3c.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)
16g.89935659T>ACA397476964TUBB3c.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)
16g.89935659T>CCA397476965TUBB3c.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
16g.89935659T>GCA397476966TUBB3c.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)
16g.89935660G>ACA397476967TUBB3c.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)
16g.89935660G>CCA397476968TUBB3c.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
16g.89935660G=CA2242020727TUBB3c.1209G= (p.Met403=)
n.4630G=
c.993G= (p.Met331=)
c.277+2082G= (n.277+2082G=)
c.*1294G= (n.*1294G=)
c.2250G= (p.Met750=)
16g.89935660G>TCA397476969TUBB3c.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)
16g.89935660_89935661insAGCA2576104232TUBB3c.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)
16g.89935661G>ACA397476972TUBB3c.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)
16g.89935661G>CCA397476970TUBB3c.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)
16g.89935661G>TCA397476971TUBB3c.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)
16g.89935662A>CCA397476973TUBB3c.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)
16g.89935662A>GCA397476974TUBB3c.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)
16g.89935662A>TCA397476975TUBB3c.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)
16g.89935663C>ACA397476976TUBB3c.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
16g.89935663C=CA2242020730TUBB3c.1212C= (p.Asp404=)
n.4633C=
c.996C= (p.Asp332=)
c.277+2085C= (n.277+2085C=)
c.*1297C= (n.*1297C=)
c.2253C= (p.Asp751=)
16g.89935663C>GCA397476977TUBB3c.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)
16g.89935663C>TCA8256222TUBB3c.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
16g.89935664G>ACA397476978TUBB3c.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
16g.89935664G>CCA397476979TUBB3c.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)
16g.89935664G=CA2242020732TUBB3c.1213G= (p.Glu405=)
n.4634G=
c.997G= (p.Glu333=)
c.277+2086G= (n.277+2086G=)
c.*1298G= (n.*1298G=)
c.2254G= (p.Glu752=)
16g.89935664G>TCA397476980TUBB3c.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)
16g.89935665A>CCA397476981TUBB3c.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)
16g.89935665A>GCA397476982TUBB3c.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)
16g.89935665A>TCA397476983TUBB3c.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)
16g.89935666G>ACA173787TUBB3c.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
16g.89935666G>CCA397476985TUBB3c.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)
16g.89935666G=CA2242020735TUBB3c.1215G= (p.Glu405=)
n.4636G=
c.999G= (p.Glu333=)
c.277+2088G= (n.277+2088G=)
c.*1300G= (n.*1300G=)
c.2256G= (p.Glu752=)
16g.89935666G>TCA397476984TUBB3c.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)
16g.89935667A=CA2242020736TUBB3c.1216A= (p.Met406=)
n.4637A=
c.1000A= (p.Met334=)
c.277+2089A= (n.277+2089A=)
c.*1301A= (n.*1301A=)
c.2257A= (p.Met753=)
16g.89935667A>CCA397476986TUBB3c.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)
16g.89935667A>GCA397476988TUBB3c.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
16g.89935667A>TCA397476987TUBB3c.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)
16g.89935668T>ACA397476989TUBB3c.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)
16g.89935668T>CCA397476990TUBB3c.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)
16g.89935668T>GCA397476991TUBB3c.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)
16g.89935669G>ACA397476992TUBB3c.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
16g.89935669G>CCA397476993TUBB3c.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)
16g.89935669G=CA2242020738TUBB3c.1218G= (p.Met406=)
n.4639G=
c.1002G= (p.Met334=)
c.277+2091G= (n.277+2091G=)
c.*1303G= (n.*1303G=)
c.2259G= (p.Met753=)
16g.89935669G>TCA397476994TUBB3c.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)
16g.89935670G>ACA397476995TUBB3c.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)
16g.89935670G>CCA397476996TUBB3c.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)
16g.89935670G>TCA397476997TUBB3c.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)
16g.89935671A>CCA397476998TUBB3c.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)
16g.89935671A>GCA397476999TUBB3c.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)
16g.89935671A>TCA397477000TUBB3c.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)
16g.89935672G>ACA497194439TUBB3c.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=)
16g.89935672G>CCA397477002TUBB3c.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)
16g.89935672G>TCA397477001TUBB3c.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)
16g.89935673T>ACA397477003TUBB3c.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)
16g.89935673T>CCA397477004TUBB3c.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)
16g.89935673T>GCA397477005TUBB3c.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)
16g.89935674T>ACA397477006TUBB3c.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)
16g.89935674T>CCA397477007TUBB3c.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)
16g.89935674T>GCA397477008TUBB3c.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)
16g.89935675C>ACA397477009TUBB3c.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)
16g.89935675C>GCA397477010TUBB3c.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)
16g.89935675C>TCA497194440TUBB3c.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=)
16g.89935676A>CCA397477011TUBB3c.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)
16g.89935676A>GCA397477012TUBB3c.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
16g.89935676A>TCA397477013TUBB3c.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)
16g.89935677C>ACA397477016TUBB3c.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)
16g.89935677C=CA2242020740TUBB3c.1226C= (p.Thr409=)
n.4647C=
c.1010C= (p.Thr337=)
c.277+2099C= (n.277+2099C=)
c.*1311C= (n.*1311C=)
c.2267C= (p.Thr756=)
16g.89935677C>GCA397477015TUBB3c.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)
16g.89935677C>TCA397477014TUBB3c.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
16g.89935678C>ACA497194441TUBB3c.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=)
16g.89935678C=CA2242020743TUBB3c.1227C= (p.Thr409=)
n.4648C=
c.1011C= (p.Thr337=)
c.277+2100C= (n.277+2100C=)
c.*1312C= (n.*1312C=)
c.2268C= (p.Thr756=)
16g.89935678C>GCA497194442TUBB3c.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=)
16g.89935678C>TCA8256223TUBB3c.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
16g.89935679G>ACA213335TUBB3c.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
16g.89935679G>CCA397477017TUBB3c.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
16g.89935679G=CA2242020746TUBB3c.1228G= (p.Glu410=)
n.4649G=
c.1012G= (p.Glu338=)
c.277+2101G= (n.277+2101G=)
c.*1313G= (n.*1313G=)
c.2269G= (p.Glu757=)
16g.89935679G>TCA397477018TUBB3c.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)
16g.89935680A>CCA397477019TUBB3c.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)
16g.89935680A>GCA397477020TUBB3c.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)
16g.89935680A>TCA397477021TUBB3c.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)
16g.89935681G>ACA497194443TUBB3c.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
16g.89935681G>CCA397477022TUBB3c.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)
16g.89935681G>TCA397477023TUBB3c.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)
16g.89935682G>ACA397477024TUBB3c.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)
16g.89935682G>CCA397477025TUBB3c.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)
16g.89935682G>TCA397477026TUBB3c.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)
16g.89935683C>ACA397477029TUBB3c.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)
16g.89935683C>GCA397477028TUBB3c.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)
16g.89935683C>TCA397477027TUBB3c.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)
16g.89935684C>ACA497194444TUBB3c.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
16g.89935684C=CA2242020754TUBB3c.1233C= (p.Ala411=)
n.4654C=
c.1017C= (p.Ala339=)
c.277+2106C= (n.277+2106C=)
c.*1318C= (n.*1318C=)
c.2274C= (p.Ala758=)
16g.89935684C>GCA497194445TUBB3c.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=)
16g.89935684C>TCA8256224TUBB3c.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
16g.89935685G>ACA397477030TUBB3c.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
16g.89935685G>CCA397477031TUBB3c.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)
16g.89935685G=CA2242020756TUBB3c.1234G= (p.Glu412=)
n.4655G=
c.1018G= (p.Glu340=)
c.277+2107G= (n.277+2107G=)
c.*1319G= (n.*1319G=)
c.2275G= (p.Glu759=)
16g.89935685G>TCA397477032TUBB3c.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)
16g.89935686A>CCA397477033TUBB3c.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)
16g.89935686A>GCA397477034TUBB3c.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)
16g.89935686A>TCA397477035TUBB3c.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)
16g.89935687G>ACA497194446TUBB3c.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
16g.89935687G>CCA397477036TUBB3c.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)
16g.89935687G>TCA397477037TUBB3c.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)
16g.89935688A>CCA397477038TUBB3c.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)
16g.89935688A>GCA397477039TUBB3c.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)
16g.89935688A>TCA397477040TUBB3c.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)
16g.89935689G>ACA397477041TUBB3c.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)
16g.89935689G>CCA397477043TUBB3c.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)
16g.89935689G>TCA397477042TUBB3c.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)
16g.89935690C>ACA397477044TUBB3c.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)
16g.89935690C>GCA397477045TUBB3c.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
16g.89935690C>TCA497194447TUBB3c.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
16g.89935691A>CCA397477046TUBB3c.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)
16g.89935691A>GCA397477048TUBB3c.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)
16g.89935691A>TCA397477047TUBB3c.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)
16g.89935692A>CCA397477049TUBB3c.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)
16g.89935692A>GCA397477051TUBB3c.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)
16g.89935692A>TCA397477050TUBB3c.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)
16g.89935693C>ACA397477052TUBB3c.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)
16g.89935693C>GCA397477053TUBB3c.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)
16g.89935693C>TCA497194449TUBB3c.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
16g.89935694A=CA2242020758TUBB3c.1243A= (p.Met415=)
n.4664A=
c.1027A= (p.Met343=)
c.277+2116A= (n.277+2116A=)
c.*1328A= (n.*1328A=)
c.2284A= (p.Met762=)
16g.89935694A>CCA397477054TUBB3c.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)
16g.89935694A>GCA397477055TUBB3c.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
16g.89935694A>TCA397477056TUBB3c.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)
16g.89935695T>ACA397477057TUBB3c.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)
16g.89935695T>CCA397477058TUBB3c.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
16g.89935695T>GCA397477059TUBB3c.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)
16g.89935695T=CA2242020760TUBB3c.1244T= (p.Met415=)
n.4665T=
c.1028T= (p.Met343=)
c.277+2117T= (n.277+2117T=)
c.*1329T= (n.*1329T=)
c.2285T= (p.Met762=)
16g.89935696G>ACA8256225TUBB3c.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
16g.89935696G>CCA397477060TUBB3c.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)
16g.89935696G=CA2242020763TUBB3c.1245G= (p.Met415=)
n.4666G=
c.1029G= (p.Met343=)
c.277+2118G= (n.277+2118G=)
c.*1330G= (n.*1330G=)
c.2286G= (p.Met762=)
16g.89935696G>TCA397477061TUBB3c.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)
16g.89935697A>CCA397477064TUBB3c.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)
16g.89935697A>GCA397477062TUBB3c.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)
16g.89935697A>TCA397477063TUBB3c.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)
16g.89935698A=CA2242020764TUBB3c.1247A= (p.Asn416=)
n.4668A=
c.1031A= (p.Asn344=)
c.277+2120A= (n.277+2120A=)
c.*1332A= (n.*1332A=)
c.2288A= (p.Asn763=)
16g.89935698A>CCA397477065TUBB3c.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)
16g.89935698A>GCA397477066TUBB3c.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
16g.89935698A>TCA397477067TUBB3c.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)
16g.89935699C>ACA397477068TUBB3c.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)
16g.89935699C=CA2242020765TUBB3c.1248C= (p.Asn416=)
n.4669C=
c.1032C= (p.Asn344=)
c.277+2121C= (n.277+2121C=)
c.*1333C= (n.*1333C=)
c.2289C= (p.Asn763=)
16g.89935699C>GCA397477069TUBB3c.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
16g.89935699C>TCA8256226TUBB3c.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
16g.89935700G>ACA340624TUBB3c.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
16g.89935700G>CCA340622TUBB3c.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
16g.89935700G=CA2242020768TUBB3c.1249G= (p.Asp417=)
n.4670G=
c.1033G= (p.Asp345=)
c.277+2122G= (n.277+2122G=)
c.*1334G= (n.*1334G=)
c.2290G= (p.Asp764=)
16g.89935700G>TCA397477070TUBB3c.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)
16g.89935701A>CCA397477073TUBB3c.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)
16g.89935701A>GCA397477072TUBB3c.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
16g.89935701A>TCA397477071TUBB3c.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)
16g.89935702C>ACA397477074TUBB3c.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)
16g.89935702C=CA2242020770TUBB3c.1251C= (p.Asp417=)
n.4672C=
c.1035C= (p.Asp345=)
c.277+2124C= (n.277+2124C=)
c.*1336C= (n.*1336C=)
c.2292C= (p.Asp764=)
16g.89935702C>GCA397477075TUBB3c.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)
16g.89935702C>TCA8256227TUBB3c.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
16g.89935703C>ACA397477076TUBB3c.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)
16g.89935703C=CA2242020771TUBB3c.1252C= (p.Leu418=)
n.4673C=
c.1036C= (p.Leu346=)
c.277+2125C= (n.277+2125C=)
c.*1337C= (n.*1337C=)
c.2293C= (p.Leu765=)
16g.89935703C>GCA397477077TUBB3c.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)
16g.89935703C>TCA497194453TUBB3c.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
16g.89935704T>ACA397477078TUBB3c.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)
16g.89935704T>CCA397477079TUBB3c.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)
16g.89935704T>GCA397477080TUBB3c.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)
16g.89935705G>ACA497194454TUBB3c.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=)
16g.89935705G>CCA8256228TUBB3c.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
16g.89935705G=CA2242020773TUBB3c.1254G= (p.Leu418=)
n.4675G=
c.1038G= (p.Leu346=)
c.277+2127G= (n.277+2127G=)
c.*1339G= (n.*1339G=)
c.2295G= (p.Leu765=)
16g.89935705G>TCA497194455TUBB3c.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=)
16g.89935706G>ACA397477081TUBB3c.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)
16g.89935706G>CCA397477082TUBB3c.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)
16g.89935706G>TCA397477083TUBB3c.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
16g.89935707T>ACA397477086TUBB3c.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)
16g.89935707T>CCA397477084TUBB3c.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)
16g.89935707T>GCA397477085TUBB3c.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)
16g.89935708G>ACA497194457TUBB3c.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
16g.89935708G>CCA497194459TUBB3c.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
16g.89935708G=CA2242020777TUBB3c.1257G= (p.Val419=)
n.4678G=
c.1041G= (p.Val347=)
c.277+2130G= (n.277+2130G=)
c.*1342G= (n.*1342G=)
c.2298G= (p.Val766=)
16g.89935708G>TCA8256229TUBB3c.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
16g.89935709T>ACA397477087TUBB3c.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)
16g.89935709T>CCA397477088TUBB3c.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)
16g.89935709T>GCA397477089TUBB3c.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)
16g.89935710C>ACA397477090TUBB3c.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)
16g.89935710C=CA2242020780TUBB3c.1259C= (p.Ser420=)
n.4680C=
c.1043C= (p.Ser348=)
c.277+2132C= (n.277+2132C=)
c.*1344C= (n.*1344C=)
c.2300C= (p.Ser767=)
16g.89935710C>GCA8256230TUBB3c.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
16g.89935710C>TCA397477091TUBB3c.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)
16g.89935711C>ACA497194461TUBB3c.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=)
16g.89935711C=CA2242020784TUBB3c.1260C= (p.Ser420=)
n.4681C=
c.1044C= (p.Ser348=)
c.277+2133C= (n.277+2133C=)
c.*1345C= (n.*1345C=)
c.2301C= (p.Ser767=)
16g.89935711C>GCA497194462TUBB3c.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
16g.89935711C>TCA8256231TUBB3c.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
16g.89935711_89935712delinsCGCA2242020783TUBB3c.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=)
16g.89935711_89935712delinsGACA286619370TUBB3c.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
16g.89935712G>ACA397477092TUBB3c.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
16g.89935712G>CCA397477093TUBB3c.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)
16g.89935712G>TCA397477094TUBB3c.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)
16g.89935713A=CA2242020785TUBB3c.1262A= (p.Glu421=)
n.4683A=
c.1046A= (p.Glu349=)
c.277+2135A= (n.277+2135A=)
c.*1347A= (n.*1347A=)
c.2303A= (p.Glu768=)
16g.89935713A>CCA397477096TUBB3c.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
16g.89935713A>GCA397477097TUBB3c.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)
16g.89935713A>TCA397477095TUBB3c.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)
16g.89935714G>ACA497194466TUBB3c.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=)
16g.89935714G>CCA397477098TUBB3c.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)
16g.89935714G>TCA397477099TUBB3c.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)
16g.89935715T>ACA397477100TUBB3c.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)
16g.89935715T>CCA397477101TUBB3c.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)
16g.89935715T>GCA397477102TUBB3c.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)
16g.89935716A>CCA397477105TUBB3c.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)
16g.89935716A>GCA397477103TUBB3c.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)
16g.89935716A>TCA397477104TUBB3c.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)
16g.89935717C>ACA397477106TUBB3c.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)
16g.89935717C>GCA397477107TUBB3c.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)
16g.89935717C>TCA497194471TUBB3c.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
16g.89935718C>ACA397477108TUBB3c.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)
16g.89935718C>GCA397477109TUBB3c.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)
16g.89935718C>TCA397477110TUBB3c.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
16g.89935719A>CCA397477113TUBB3c.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)
16g.89935719A>GCA397477111TUBB3c.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)
16g.89935719A>TCA397477112TUBB3c.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)
16g.89935720G>ACA497194473TUBB3c.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
16g.89935720G>CCA397477114TUBB3c.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)
16g.89935720G=CA2242020786TUBB3c.1269G= (p.Gln423=)
n.4690G=
c.1053G= (p.Gln351=)
c.277+2142G= (n.277+2142G=)
c.*1354G= (n.*1354G=)
c.2310G= (p.Gln770=)
16g.89935720G>TCA397477115TUBB3c.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)
16g.89935721C>ACA397477116TUBB3c.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)
16g.89935721C>GCA397477117TUBB3c.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)
16g.89935721C>TCA397477118TUBB3c.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)
16g.89935722A>CCA397477119TUBB3c.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
16g.89935722A>GCA397477120TUBB3c.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)
16g.89935722A>TCA397477121TUBB3c.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)
16g.89935723G>ACA497194478TUBB3c.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
16g.89935723G>CCA397477122TUBB3c.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)
16g.89935723G>TCA397477123TUBB3c.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)
16g.89935724T>ACA397477124TUBB3c.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)
16g.89935724T>CCA397477125TUBB3c.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)
16g.89935724T>GCA397477126TUBB3c.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)
16g.89935725A>CCA397477127TUBB3c.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)
16g.89935725A>GCA397477129TUBB3c.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)
16g.89935725A>TCA397477128TUBB3c.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)
16g.89935726C>ACA397477130TUBB3c.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)
16g.89935726C=CA2242020788TUBB3c.1275C= (p.Tyr425=)
n.4696C=
c.1059C= (p.Tyr353=)
c.277+2148C= (n.277+2148C=)
c.*1360C= (n.*1360C=)
c.2316C= (p.Tyr772=)
16g.89935726C>GCA397477131TUBB3c.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)
16g.89935726C>TCA497194482TUBB3c.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
16g.89935727C>ACA397477132TUBB3c.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)
16g.89935727C=CA2242020790TUBB3c.1276C= (p.Gln426=)
n.4697C=
c.1060C= (p.Gln354=)
c.277+2149C= (n.277+2149C=)
c.*1361C= (n.*1361C=)
c.2317C= (p.Gln773=)
16g.89935727C>GCA397477133TUBB3c.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
16g.89935727C>TCA397477134TUBB3c.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
16g.89935728A>CCA397477135TUBB3c.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
16g.89935728A>GCA397477136TUBB3c.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)
16g.89935728A>TCA397477137TUBB3c.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)
16g.89935729G>ACA497194484TUBB3c.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=)
16g.89935729G>CCA397477138TUBB3c.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)
16g.89935729G>TCA397477139TUBB3c.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)
16g.89935730G>ACA397477140TUBB3c.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
16g.89935730G>CCA397477141TUBB3c.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)
16g.89935730G>TCA397477142TUBB3c.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)
16g.89935731A>CCA397477145TUBB3c.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)
16g.89935731A>GCA397477143TUBB3c.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
16g.89935731A>TCA397477144TUBB3c.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)
16g.89935732C>ACA397477146TUBB3c.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)
16g.89935732C=CA2242020791TUBB3c.1281C= (p.Asp427=)
n.4702C=
c.1065C= (p.Asp355=)
c.277+2154C= (n.277+2154C=)
c.*1366C= (n.*1366C=)
c.2322C= (p.Asp774=)
16g.89935732C>GCA397477147TUBB3c.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
16g.89935732C>TCA8256232TUBB3c.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
16g.89935733G>ACA397477148TUBB3c.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
16g.89935733G>CCA397477149TUBB3c.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)
16g.89935733G>TCA397477150TUBB3c.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
16g.89935734C>ACA397477151TUBB3c.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)
16g.89935734C=CA2242020792TUBB3c.1283C= (p.Ala428=)
n.4704C=
c.1067C= (p.Ala356=)
c.277+2156C= (n.277+2156C=)
c.*1368C= (n.*1368C=)
c.2324C= (p.Ala775=)
16g.89935734C>GCA397477152TUBB3c.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)
16g.89935734C>TCA397477153TUBB3c.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
16g.89935735C>ACA497194490TUBB3c.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=)
16g.89935735C>GCA497194491TUBB3c.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=)
16g.89935735C>TCA497194492TUBB3c.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
16g.89935736A>CCA397477154TUBB3c.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)
16g.89935736A>GCA397477155TUBB3c.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)
16g.89935736A>TCA397477156TUBB3c.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)
16g.89935737C>ACA397477157TUBB3c.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)
16g.89935737C=CA2242020796TUBB3c.1286C= (p.Thr429=)
n.4707C=
c.1070C= (p.Thr357=)
c.277+2159C= (n.277+2159C=)
c.*1371C= (n.*1371C=)
c.2327C= (p.Thr776=)
16g.89935737C>GCA397477158TUBB3c.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)
16g.89935737C>TCA8256233TUBB3c.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
16g.89935738G>ACA209122TUBB3c.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
16g.89935738G>CCA497194497TUBB3c.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=)
16g.89935738G=CA2242020806TUBB3c.1287G= (p.Thr429=)
n.4708G=
c.1071G= (p.Thr357=)
c.277+2160G= (n.277+2160G=)
c.*1372G= (n.*1372G=)
c.2328G= (p.Thr776=)
16g.89935738G>TCA8256234TUBB3c.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
16g.89935739G>ACA397477159TUBB3c.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)
16g.89935739G>CCA350350TUBB3c.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
16g.89935739G=CA2242020810TUBB3c.1288G= (p.Ala430=)
n.4709G=
c.1072G= (p.Ala358=)
c.277+2161G= (n.277+2161G=)
c.*1373G= (n.*1373G=)
c.2329G= (p.Ala777=)
16g.89935739G>TCA397477160TUBB3c.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)
16g.89935740C>ACA397477161TUBB3c.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)
16g.89935740C>GCA397477162TUBB3c.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)
16g.89935740C>TCA397477163TUBB3c.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)
16g.89935741C>ACA497194502TUBB3c.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=)
16g.89935741C=CA2242020812TUBB3c.1290C= (p.Ala430=)
n.4711C=
c.1074C= (p.Ala358=)
c.277+2163C= (n.277+2163C=)
c.*1375C= (n.*1375C=)
c.2331C= (p.Ala777=)
16g.89935741C>GCA497194504TUBB3c.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=)
16g.89935741C>TCA8256235TUBB3c.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
16g.89935742G>ACA286619400TUBB3c.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
16g.89935742G>CCA397477164TUBB3c.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)
16g.89935742G=CA2242020815TUBB3c.1291G= (p.Glu431=)
n.4712G=
c.1075G= (p.Glu359=)
c.277+2164G= (n.277+2164G=)
c.*1376G= (n.*1376G=)
c.2332G= (p.Glu778=)
16g.89935742G>TCA397477165TUBB3c.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
16g.89935743A>CCA397477168TUBB3c.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)
16g.89935743A>GCA397477167TUBB3c.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)
16g.89935743A>TCA397477166TUBB3c.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)
16g.89935744G>ACA497194507TUBB3c.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=)
16g.89935744G>CCA397477169TUBB3c.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)
16g.89935744G>TCA397477170TUBB3c.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
16g.89935745G>ACA397477171TUBB3c.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)
16g.89935745G>CCA397477172TUBB3c.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)
16g.89935745G>TCA397477173TUBB3c.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)
16g.89935747_89935749dupCA2635070901TUBB3c.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
16g.89935746A>CCA397477174TUBB3c.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)
16g.89935746A>GCA397477175TUBB3c.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
16g.89935746A>TCA397477176TUBB3c.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)

Number of alleles fetched