Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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) | |
16 | g.89935760T>A | CA397477208 | TUBB3 | c.1309T>A (p.Tyr437Asn) n.4730T>A c.1093T>A (p.Tyr365Asn) c.277+2182T>A (n.277+2182T>A) c.*1394T>A (n.*1394T>A) c.2350T>A (p.Tyr784Asn) | |
16 | g.89935760T>C | CA397477209 | TUBB3 | c.1309T>C (p.Tyr437His) n.4730T>C c.1093T>C (p.Tyr365His) c.277+2182T>C (n.277+2182T>C) c.*1394T>C (n.*1394T>C) c.2350T>C (p.Tyr784His) | |
16 | g.89935760T>G | CA397477210 | TUBB3 | c.1309T>G (p.Tyr437Asp) n.4730T>G c.1093T>G (p.Tyr365Asp) c.277+2182T>G (n.277+2182T>G) c.*1394T>G (n.*1394T>G) c.2350T>G (p.Tyr784Asp) | |
16 | g.89935761A>C | CA397477212 | TUBB3 | c.1310A>C (p.Tyr437Ser) n.4731A>C c.1094A>C (p.Tyr365Ser) c.277+2183A>C (n.277+2183A>C) c.*1395A>C (n.*1395A>C) c.2351A>C (p.Tyr784Ser) | |
16 | g.89935761A>G | CA397477213 | TUBB3 | c.1310A>G (p.Tyr437Cys) n.4731A>G c.1094A>G (p.Tyr365Cys) c.277+2183A>G (n.277+2183A>G) c.*1395A>G (n.*1395A>G) c.2351A>G (p.Tyr784Cys) | gnomAD v4 |
16 | g.89935761A>T | CA397477211 | TUBB3 | c.1310A>T (p.Tyr437Phe) n.4731A>T c.1094A>T (p.Tyr365Phe) c.277+2183A>T (n.277+2183A>T) c.*1395A>T (n.*1395A>T) c.2351A>T (p.Tyr784Phe) | |
16 | g.89935762C>A | CA397477214 | TUBB3 | c.1311C>A (p.Tyr437Ter) n.4732C>A c.1095C>A (p.Tyr365Ter) c.277+2184C>A (n.277+2184C>A) c.*1396C>A (n.*1396C>A) c.2352C>A (p.Tyr784Ter) | |
16 | g.89935762C= | CA2242020841 | TUBB3 | c.1311C= (p.Tyr437=) n.4732C= c.1095C= (p.Tyr365=) c.277+2184C= (n.277+2184C=) c.*1396C= (n.*1396C=) c.2352C= (p.Tyr784=) | |
16 | g.89935762C>G | CA397477215 | TUBB3 | c.1311C>G (p.Tyr437Ter) n.4732C>G c.1095C>G (p.Tyr365Ter) c.277+2184C>G (n.277+2184C>G) c.*1396C>G (n.*1396C>G) c.2352C>G (p.Tyr784Ter) | |
16 | g.89935762C>T | CA8256240 | TUBB3 | c.1311C>T (p.Tyr437=) n.4732C>T c.1095C>T (p.Tyr365=) c.277+2184C>T (n.277+2184C>T) c.*1396C>T (n.*1396C>T) c.2352C>T (p.Tyr784=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935763G>A | CA286619412 | TUBB3 | c.1312G>A (p.Glu438Lys) n.4733G>A c.1096G>A (p.Glu366Lys) c.277+2185G>A (n.277+2185G>A) c.*1397G>A (n.*1397G>A) c.2353G>A (p.Glu785Lys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
16 | g.89935763G>C | CA397477216 | TUBB3 | c.1312G>C (p.Glu438Gln) n.4733G>C c.1096G>C (p.Glu366Gln) c.277+2185G>C (n.277+2185G>C) c.*1397G>C (n.*1397G>C) c.2353G>C (p.Glu785Gln) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
16 | g.89935763G= | CA2242020843 | TUBB3 | c.1312G= (p.Glu438=) n.4733G= c.1096G= (p.Glu366=) c.277+2185G= (n.277+2185G=) c.*1397G= (n.*1397G=) c.2353G= (p.Glu785=) | |
16 | g.89935763G>T | CA286619415 | TUBB3 | c.1312G>T (p.Glu438Ter) n.4733G>T c.1096G>T (p.Glu366Ter) c.277+2185G>T (n.277+2185G>T) c.*1397G>T (n.*1397G>T) c.2353G>T (p.Glu785Ter) | dbSNP |
16 | g.89935764A= | CA2242020846 | TUBB3 | c.1313A= (p.Glu438=) n.4734A= c.1097A= (p.Glu366=) c.277+2186A= (n.277+2186A=) c.*1398A= (n.*1398A=) c.2354A= (p.Glu785=) | |
16 | g.89935764A>C | CA397477217 | TUBB3 | c.1313A>C (p.Glu438Ala) n.4734A>C c.1097A>C (p.Glu366Ala) c.277+2186A>C (n.277+2186A>C) c.*1398A>C (n.*1398A>C) c.2354A>C (p.Glu785Ala) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.89935764A>G | CA397477218 | TUBB3 | c.1313A>G (p.Glu438Gly) n.4734A>G c.1097A>G (p.Glu366Gly) c.277+2186A>G (n.277+2186A>G) c.*1398A>G (n.*1398A>G) c.2354A>G (p.Glu785Gly) | |
16 | g.89935764A>T | CA397477219 | TUBB3 | c.1313A>T (p.Glu438Val) n.4734A>T c.1097A>T (p.Glu366Val) c.277+2186A>T (n.277+2186A>T) c.*1398A>T (n.*1398A>T) c.2354A>T (p.Glu785Val) | |
16 | g.89935765A>C | CA397477220 | TUBB3 | c.1314A>C (p.Glu438Asp) n.4735A>C c.1098A>C (p.Glu366Asp) c.277+2187A>C (n.277+2187A>C) c.*1399A>C (n.*1399A>C) c.2355A>C (p.Glu785Asp) | |
16 | g.89935765A>G | CA497194543 | TUBB3 | c.1314A>G (p.Glu438=) n.4735A>G c.1098A>G (p.Glu366=) c.277+2187A>G (n.277+2187A>G) c.*1399A>G (n.*1399A>G) c.2355A>G (p.Glu785=) | |
16 | g.89935765A>T | CA397477221 | TUBB3 | c.1314A>T (p.Glu438Asp) n.4735A>T c.1098A>T (p.Glu366Asp) c.277+2187A>T (n.277+2187A>T) c.*1399A>T (n.*1399A>T) c.2355A>T (p.Glu785Asp) | |
16 | g.89935766G>A | CA397477222 | TUBB3 | c.1315G>A (p.Asp439Asn) n.4736G>A c.1099G>A (p.Asp367Asn) c.277+2188G>A (n.277+2188G>A) c.*1400G>A (n.*1400G>A) c.2356G>A (p.Asp786Asn) | gnomAD v4 |
16 | g.89935766G>C | CA397477223 | TUBB3 | c.1315G>C (p.Asp439His) n.4736G>C c.1099G>C (p.Asp367His) c.277+2188G>C (n.277+2188G>C) c.*1400G>C (n.*1400G>C) c.2356G>C (p.Asp786His) | |
16 | g.89935766G>T | CA397477224 | TUBB3 | c.1315G>T (p.Asp439Tyr) n.4736G>T c.1099G>T (p.Asp367Tyr) c.277+2188G>T (n.277+2188G>T) c.*1400G>T (n.*1400G>T) c.2356G>T (p.Asp786Tyr) | gnomAD v4 |
16 | g.89935771_89935773del | CA912996822 | TUBB3 | c.1320_1322del (p.Asp440del) n.4741_4743del c.1104_1106del (p.Asp368del) c.277+2193_277+2195del (n.277+2193_277+2195del) c.*1405_*1407del (n.*1405_*1407del) c.2361_2363del (p.Asp787del) | |
16 | g.89935767A>C | CA397477227 | TUBB3 | c.1316A>C (p.Asp439Ala) n.4737A>C c.1100A>C (p.Asp367Ala) c.277+2189A>C (n.277+2189A>C) c.*1401A>C (n.*1401A>C) c.2357A>C (p.Asp786Ala) | |
16 | g.89935767A>G | CA397477225 | TUBB3 | c.1316A>G (p.Asp439Gly) n.4737A>G c.1100A>G (p.Asp367Gly) c.277+2189A>G (n.277+2189A>G) c.*1401A>G (n.*1401A>G) c.2357A>G (p.Asp786Gly) | gnomAD v4 |
16 | g.89935767A>T | CA397477226 | TUBB3 | c.1316A>T (p.Asp439Val) n.4737A>T c.1100A>T (p.Asp367Val) c.277+2189A>T (n.277+2189A>T) c.*1401A>T (n.*1401A>T) c.2357A>T (p.Asp786Val) | |
16 | g.89935768C>A | CA8256242 | TUBB3 | c.1317C>A (p.Asp439Glu) n.4738C>A c.1101C>A (p.Asp367Glu) c.277+2190C>A (n.277+2190C>A) c.*1402C>A (n.*1402C>A) c.2358C>A (p.Asp786Glu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.89935768C= | CA2242020851 | TUBB3 | c.1317C= (p.Asp439=) n.4738C= c.1101C= (p.Asp367=) c.277+2190C= (n.277+2190C=) c.*1402C= (n.*1402C=) c.2358C= (p.Asp786=) | |
16 | g.89935768C>G | CA397477228 | TUBB3 | c.1317C>G (p.Asp439Glu) n.4738C>G c.1101C>G (p.Asp367Glu) c.277+2190C>G (n.277+2190C>G) c.*1402C>G (n.*1402C>G) c.2358C>G (p.Asp786Glu) | gnomAD v4 |
16 | g.89935768C>T | CA8256241 | TUBB3 | c.1317C>T (p.Asp439=) n.4738C>T c.1101C>T (p.Asp367=) c.277+2190C>T (n.277+2190C>T) c.*1402C>T (n.*1402C>T) c.2358C>T (p.Asp786=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935769G>A | CA8256243 | TUBB3 | c.1318G>A (p.Asp440Asn) n.4739G>A c.1102G>A (p.Asp368Asn) c.277+2191G>A (n.277+2191G>A) c.*1403G>A (n.*1403G>A) c.2359G>A (p.Asp787Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.89935769G>C | CA397477229 | TUBB3 | c.1318G>C (p.Asp440His) n.4739G>C c.1102G>C (p.Asp368His) c.277+2191G>C (n.277+2191G>C) c.*1403G>C (n.*1403G>C) c.2359G>C (p.Asp787His) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
16 | g.89935769G= | CA2242020857 | TUBB3 | c.1318G= (p.Asp440=) n.4739G= c.1102G= (p.Asp368=) c.277+2191G= (n.277+2191G=) c.*1403G= (n.*1403G=) c.2359G= (p.Asp787=) | |
16 | g.89935769G>T | CA397477230 | TUBB3 | c.1318G>T (p.Asp440Tyr) n.4739G>T c.1102G>T (p.Asp368Tyr) c.277+2191G>T (n.277+2191G>T) c.*1403G>T (n.*1403G>T) c.2359G>T (p.Asp787Tyr) | |
16 | g.89935770A= | CA2242020860 | TUBB3 | c.1319A= (p.Asp440=) n.4740A= c.1103A= (p.Asp368=) c.277+2192A= (n.277+2192A=) c.*1404A= (n.*1404A=) c.2360A= (p.Asp787=) | |
16 | g.89935770A>C | CA397477231 | TUBB3 | c.1319A>C (p.Asp440Ala) n.4740A>C c.1103A>C (p.Asp368Ala) c.277+2192A>C (n.277+2192A>C) c.*1404A>C (n.*1404A>C) c.2360A>C (p.Asp787Ala) | dbSNP |
16 | g.89935770A>G | CA397477232 | TUBB3 | c.1319A>G (p.Asp440Gly) n.4740A>G c.1103A>G (p.Asp368Gly) c.277+2192A>G (n.277+2192A>G) c.*1404A>G (n.*1404A>G) c.2360A>G (p.Asp787Gly) | |
16 | g.89935770A>T | CA397477233 | TUBB3 | c.1319A>T (p.Asp440Val) n.4740A>T c.1103A>T (p.Asp368Val) c.277+2192A>T (n.277+2192A>T) c.*1404A>T (n.*1404A>T) c.2360A>T (p.Asp787Val) | gnomAD v4 |
16 | g.89935771C>A | CA397477234 | TUBB3 | c.1320C>A (p.Asp440Glu) n.4741C>A c.1104C>A (p.Asp368Glu) c.277+2193C>A (n.277+2193C>A) c.*1405C>A (n.*1405C>A) c.2361C>A (p.Asp787Glu) | gnomAD v4 |
16 | g.89935771C= | CA2242020863 | TUBB3 | c.1320C= (p.Asp440=) n.4741C= c.1104C= (p.Asp368=) c.277+2193C= (n.277+2193C=) c.*1405C= (n.*1405C=) c.2361C= (p.Asp787=) | |
16 | g.89935771C>G | CA397477235 | TUBB3 | c.1320C>G (p.Asp440Glu) n.4741C>G c.1104C>G (p.Asp368Glu) c.277+2193C>G (n.277+2193C>G) c.*1405C>G (n.*1405C>G) c.2361C>G (p.Asp787Glu) | |
16 | g.89935771C>T | CA497194550 | TUBB3 | c.1320C>T (p.Asp440=) n.4741C>T c.1104C>T (p.Asp368=) c.277+2193C>T (n.277+2193C>T) c.*1405C>T (n.*1405C>T) c.2361C>T (p.Asp787=) | dbSNP gnomAD v4 |
16 | g.89935771_89935774delinsCGAG | CA2242020864 | TUBB3 | c.1320_1323delinsCGAG (p.Asp440=) n.4741_4744delinsCGAG c.1104_1107delinsCGAG (p.Asp368=) c.277+2193_277+2196delinsCGAG (n.277+2193_277+2196delinsCGAG) c.*1405_*1408delinsCGAG (n.*1405_*1408delinsCGAG) c.2361_2364delinsCGAG (p.Asp787=) | |
16 | g.89935772G>A | CA8256244 | TUBB3 | c.1321G>A (p.Glu441Lys) n.4742G>A c.1105G>A (p.Glu369Lys) c.277+2194G>A (n.277+2194G>A) c.*1406G>A (n.*1406G>A) c.2362G>A (p.Glu788Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935772G>C | CA397477237 | TUBB3 | c.1321G>C (p.Glu441Gln) n.4742G>C c.1105G>C (p.Glu369Gln) c.277+2194G>C (n.277+2194G>C) c.*1406G>C (n.*1406G>C) c.2362G>C (p.Glu788Gln) | dbSNP |
16 | g.89935772G= | CA2242020872 | TUBB3 | c.1321G= (p.Glu441=) n.4742G= c.1105G= (p.Glu369=) c.277+2194G= (n.277+2194G=) c.*1406G= (n.*1406G=) c.2362G= (p.Glu788=) | |
16 | g.89935772G>T | CA397477236 | TUBB3 | c.1321G>T (p.Glu441Ter) n.4742G>T c.1105G>T (p.Glu369Ter) c.277+2194G>T (n.277+2194G>T) c.*1406G>T (n.*1406G>T) c.2362G>T (p.Glu788Ter) | |
16 | g.89935778_89935780del | CA725740427 | TUBB3 | c.1327_1329del (p.Glu443del) n.4748_4750del c.1111_1113del (p.Glu371del) c.277+2200_277+2202del (n.277+2200_277+2202del) c.*1412_*1414del (n.*1412_*1414del) c.2368_2370del (p.Glu790del) | dbSNP gnomAD v4 |
16 | g.89935773A>C | CA397477238 | TUBB3 | c.1322A>C (p.Glu441Ala) n.4743A>C c.1106A>C (p.Glu369Ala) c.277+2195A>C (n.277+2195A>C) c.*1407A>C (n.*1407A>C) c.2363A>C (p.Glu788Ala) | |
16 | g.89935773A>G | CA397477239 | TUBB3 | c.1322A>G (p.Glu441Gly) n.4743A>G c.1106A>G (p.Glu369Gly) c.277+2195A>G (n.277+2195A>G) c.*1407A>G (n.*1407A>G) c.2363A>G (p.Glu788Gly) | |
16 | g.89935773A>T | CA397477240 | TUBB3 | c.1322A>T (p.Glu441Val) n.4743A>T c.1106A>T (p.Glu369Val) c.277+2195A>T (n.277+2195A>T) c.*1407A>T (n.*1407A>T) c.2363A>T (p.Glu788Val) | |
16 | g.89935774G>A | CA497194553 | TUBB3 | c.1323G>A (p.Glu441=) n.4744G>A c.1107G>A (p.Glu369=) c.277+2196G>A (n.277+2196G>A) c.*1408G>A (n.*1408G>A) c.2364G>A (p.Glu788=) | |
16 | g.89935774G>C | CA8256245 | TUBB3 | c.1323G>C (p.Glu441Asp) n.4744G>C c.1107G>C (p.Glu369Asp) c.277+2196G>C (n.277+2196G>C) c.*1408G>C (n.*1408G>C) c.2364G>C (p.Glu788Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935774G= | CA2242020875 | TUBB3 | c.1323G= (p.Glu441=) n.4744G= c.1107G= (p.Glu369=) c.277+2196G= (n.277+2196G=) c.*1408G= (n.*1408G=) c.2364G= (p.Glu788=) | |
16 | g.89935774G>T | CA397477241 | TUBB3 | c.1323G>T (p.Glu441Asp) n.4744G>T c.1107G>T (p.Glu369Asp) c.277+2196G>T (n.277+2196G>T) c.*1408G>T (n.*1408G>T) c.2364G>T (p.Glu788Asp) | COSMIC |
16 | g.89935775G>A | CA397477244 | TUBB3 | c.1324G>A (p.Glu442Lys) n.4745G>A c.1108G>A (p.Glu370Lys) c.277+2197G>A (n.277+2197G>A) c.*1409G>A (n.*1409G>A) c.2365G>A (p.Glu789Lys) | gnomAD v4 COSMIC |
16 | g.89935775G>C | CA397477243 | TUBB3 | c.1324G>C (p.Glu442Gln) n.4745G>C c.1108G>C (p.Glu370Gln) c.277+2197G>C (n.277+2197G>C) c.*1409G>C (n.*1409G>C) c.2365G>C (p.Glu789Gln) | |
16 | g.89935775G>T | CA397477242 | TUBB3 | c.1324G>T (p.Glu442Ter) n.4745G>T c.1108G>T (p.Glu370Ter) c.277+2197G>T (n.277+2197G>T) c.*1409G>T (n.*1409G>T) c.2365G>T (p.Glu789Ter) | COSMIC |
16 | g.89935776A= | CA2242020878 | TUBB3 | c.1325A= (p.Glu442=) n.4746A= c.1109A= (p.Glu370=) c.277+2198A= (n.277+2198A=) c.*1410A= (n.*1410A=) c.2366A= (p.Glu789=) | |
16 | g.89935776A>C | CA397477245 | TUBB3 | c.1325A>C (p.Glu442Ala) n.4746A>C c.1109A>C (p.Glu370Ala) c.277+2198A>C (n.277+2198A>C) c.*1410A>C (n.*1410A>C) c.2366A>C (p.Glu789Ala) | |
16 | g.89935776A>G | CA397477246 | TUBB3 | c.1325A>G (p.Glu442Gly) n.4746A>G c.1109A>G (p.Glu370Gly) c.277+2198A>G (n.277+2198A>G) c.*1410A>G (n.*1410A>G) c.2366A>G (p.Glu789Gly) | |
16 | g.89935776A>T | CA397477247 | TUBB3 | c.1325A>T (p.Glu442Val) n.4746A>T c.1109A>T (p.Glu370Val) c.277+2198A>T (n.277+2198A>T) c.*1410A>T (n.*1410A>T) c.2366A>T (p.Glu789Val) | dbSNP |
16 | g.89935777G>A | CA8256246 | TUBB3 | c.1326G>A (p.Glu442=) n.4747G>A c.1110G>A (p.Glu370=) c.277+2199G>A (n.277+2199G>A) c.*1411G>A (n.*1411G>A) c.2367G>A (p.Glu789=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935777G>C | CA397477248 | TUBB3 | c.1326G>C (p.Glu442Asp) n.4747G>C c.1110G>C (p.Glu370Asp) c.277+2199G>C (n.277+2199G>C) c.*1411G>C (n.*1411G>C) c.2367G>C (p.Glu789Asp) | |
16 | g.89935777G= | CA2242020882 | TUBB3 | c.1326G= (p.Glu442=) n.4747G= c.1110G= (p.Glu370=) c.277+2199G= (n.277+2199G=) c.*1411G= (n.*1411G=) c.2367G= (p.Glu789=) | |
16 | g.89935777G>T | CA397477249 | TUBB3 | c.1326G>T (p.Glu442Asp) n.4747G>T c.1110G>T (p.Glu370Asp) c.277+2199G>T (n.277+2199G>T) c.*1411G>T (n.*1411G>T) c.2367G>T (p.Glu789Asp) | |
16 | g.89935778G>A | CA397477250 | TUBB3 | c.1327G>A (p.Glu443Lys) n.4748G>A c.1111G>A (p.Glu371Lys) c.277+2200G>A (n.277+2200G>A) c.*1412G>A (n.*1412G>A) c.2368G>A (p.Glu790Lys) | |
16 | g.89935778G>C | CA397477252 | TUBB3 | c.1327G>C (p.Glu443Gln) n.4748G>C c.1111G>C (p.Glu371Gln) c.277+2200G>C (n.277+2200G>C) c.*1412G>C (n.*1412G>C) c.2368G>C (p.Glu790Gln) | gnomAD v4 |
16 | g.89935778G= | CA2242020885 | TUBB3 | c.1327G= (p.Glu443=) n.4748G= c.1111G= (p.Glu371=) c.277+2200G= (n.277+2200G=) c.*1412G= (n.*1412G=) c.2368G= (p.Glu790=) | |
16 | g.89935778G>T | CA397477251 | TUBB3 | c.1327G>T (p.Glu443Ter) n.4748G>T c.1111G>T (p.Glu371Ter) c.277+2200G>T (n.277+2200G>T) c.*1412G>T (n.*1412G>T) c.2368G>T (p.Glu790Ter) | dbSNP gnomAD v2 |
16 | g.89935779A= | CA2242020887 | TUBB3 | c.1328A= (p.Glu443=) n.4749A= c.1112A= (p.Glu371=) c.277+2201A= (n.277+2201A=) c.*1413A= (n.*1413A=) c.2369A= (p.Glu790=) | |
16 | g.89935779A>C | CA397477253 | TUBB3 | c.1328A>C (p.Glu443Ala) n.4749A>C c.1112A>C (p.Glu371Ala) c.277+2201A>C (n.277+2201A>C) c.*1413A>C (n.*1413A>C) c.2369A>C (p.Glu790Ala) | |
16 | g.89935779A>G | CA397477254 | TUBB3 | c.1328A>G (p.Glu443Gly) n.4749A>G c.1112A>G (p.Glu371Gly) c.277+2201A>G (n.277+2201A>G) c.*1413A>G (n.*1413A>G) c.2369A>G (p.Glu790Gly) | gnomAD v4 |
16 | g.89935779A>T | CA397477255 | TUBB3 | c.1328A>T (p.Glu443Val) n.4749A>T c.1112A>T (p.Glu371Val) c.277+2201A>T (n.277+2201A>T) c.*1413A>T (n.*1413A>T) c.2369A>T (p.Glu790Val) | dbSNP gnomAD v2 |
16 | g.89935780G>A | CA8256248 | TUBB3 | c.1329G>A (p.Glu443=) n.4750G>A c.1113G>A (p.Glu371=) c.277+2202G>A (n.277+2202G>A) c.*1414G>A (n.*1414G>A) c.2370G>A (p.Glu790=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.89935780G>C | CA8256247 | TUBB3 | c.1329G>C (p.Glu443Asp) n.4750G>C c.1113G>C (p.Glu371Asp) c.277+2202G>C (n.277+2202G>C) c.*1414G>C (n.*1414G>C) c.2370G>C (p.Glu790Asp) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.89935780G= | CA2242020891 | TUBB3 | c.1329G= (p.Glu443=) n.4750G= c.1113G= (p.Glu371=) c.277+2202G= (n.277+2202G=) c.*1414G= (n.*1414G=) c.2370G= (p.Glu790=) | |
16 | g.89935780G>T | CA397477256 | TUBB3 | c.1329G>T (p.Glu443Asp) n.4750G>T c.1113G>T (p.Glu371Asp) c.277+2202G>T (n.277+2202G>T) c.*1414G>T (n.*1414G>T) c.2370G>T (p.Glu790Asp) | gnomAD v4 |
16 | g.89935781T>A | CA397477257 | TUBB3 | c.1330T>A (p.Ser444Thr) n.4751T>A c.1114T>A (p.Ser372Thr) c.277+2203T>A (n.277+2203T>A) c.*1415T>A (n.*1415T>A) c.2371T>A (p.Ser791Thr) | |
16 | g.89935781T>C | CA397477258 | TUBB3 | c.1330T>C (p.Ser444Pro) n.4751T>C c.1114T>C (p.Ser372Pro) c.277+2203T>C (n.277+2203T>C) c.*1415T>C (n.*1415T>C) c.2371T>C (p.Ser791Pro) | |
16 | g.89935781T>G | CA397477259 | TUBB3 | c.1330T>G (p.Ser444Ala) n.4751T>G c.1114T>G (p.Ser372Ala) c.277+2203T>G (n.277+2203T>G) c.*1415T>G (n.*1415T>G) c.2371T>G (p.Ser791Ala) | |
16 | g.89935782C>A | CA397477260 | TUBB3 | c.1331C>A (p.Ser444Ter) n.4752C>A c.1115C>A (p.Ser372Ter) c.277+2204C>A (n.277+2204C>A) c.*1416C>A (n.*1416C>A) c.2372C>A (p.Ser791Ter) | |
16 | g.89935782C= | CA2242020896 | TUBB3 | c.1331C= (p.Ser444=) n.4752C= c.1115C= (p.Ser372=) c.277+2204C= (n.277+2204C=) c.*1416C= (n.*1416C=) c.2372C= (p.Ser791=) | |
16 | g.89935782C>G | CA397477261 | TUBB3 | c.1331C>G (p.Ser444Trp) n.4752C>G c.1115C>G (p.Ser372Trp) c.277+2204C>G (n.277+2204C>G) c.*1416C>G (n.*1416C>G) c.2372C>G (p.Ser791Trp) | |
16 | g.89935782C>T | CA173790 | TUBB3 | c.1331C>T (p.Ser444Leu) n.4752C>T c.1115C>T (p.Ser372Leu) c.277+2204C>T (n.277+2204C>T) c.*1416C>T (n.*1416C>T) c.2372C>T (p.Ser791Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
16 | g.89935783G>A | CA8256249 | TUBB3 | c.1332G>A (p.Ser444=) n.4753G>A c.1116G>A (p.Ser372=) c.277+2205G>A (n.277+2205G>A) c.*1417G>A (n.*1417G>A) c.2373G>A (p.Ser791=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935783G>C | CA497194558 | TUBB3 | c.1332G>C (p.Ser444=) n.4753G>C c.1116G>C (p.Ser372=) c.277+2205G>C (n.277+2205G>C) c.*1417G>C (n.*1417G>C) c.2373G>C (p.Ser791=) | |
16 | g.89935783G= | CA2242020904 | TUBB3 | c.1332G= (p.Ser444=) n.4753G= c.1116G= (p.Ser372=) c.277+2205G= (n.277+2205G=) c.*1417G= (n.*1417G=) c.2373G= (p.Ser791=) | |
16 | g.89935783G>T | CA497194560 | TUBB3 | c.1332G>T (p.Ser444=) n.4753G>T c.1116G>T (p.Ser372=) c.277+2205G>T (n.277+2205G>T) c.*1417G>T (n.*1417G>T) c.2373G>T (p.Ser791=) | |
16 | g.89935783_89935784insACA | CA2808106928 | TUBB3 | c.1332_1333insACA (p.Ser444_Glu445insThr) n.4753_4754insACA c.1116_1117insACA (p.Ser372_Glu373insThr) c.277+2205_277+2206insACA (n.277+2205_277+2206insACA) c.*1417_*1418insACA (n.*1417_*1418insACA) c.2373_2374insACA (p.Ser791_Glu792insThr) | |
16 | g.89935784G>A | CA397477263 | TUBB3 | c.1333G>A (p.Glu445Lys) n.4754G>A c.1117G>A (p.Glu373Lys) c.277+2206G>A (n.277+2206G>A) c.*1418G>A (n.*1418G>A) c.2374G>A (p.Glu792Lys) | |
16 | g.89935784G>C | CA397477262 | TUBB3 | c.1333G>C (p.Glu445Gln) n.4754G>C c.1117G>C (p.Glu373Gln) c.277+2206G>C (n.277+2206G>C) c.*1418G>C (n.*1418G>C) c.2374G>C (p.Glu792Gln) | gnomAD v4 |
16 | g.89935784G>T | CA397477264 | TUBB3 | c.1333G>T (p.Glu445Ter) n.4754G>T c.1117G>T (p.Glu373Ter) c.277+2206G>T (n.277+2206G>T) c.*1418G>T (n.*1418G>T) c.2374G>T (p.Glu792Ter) | gnomAD v4 |
16 | g.89935785A>C | CA397477265 | TUBB3 | c.1334A>C (p.Glu445Ala) n.4755A>C c.1118A>C (p.Glu373Ala) c.277+2207A>C (n.277+2207A>C) c.*1419A>C (n.*1419A>C) c.2375A>C (p.Glu792Ala) | |
16 | g.89935785A>G | CA397477267 | TUBB3 | c.1334A>G (p.Glu445Gly) n.4755A>G c.1118A>G (p.Glu373Gly) c.277+2207A>G (n.277+2207A>G) c.*1419A>G (n.*1419A>G) c.2375A>G (p.Glu792Gly) | |
16 | g.89935785A>T | CA397477266 | TUBB3 | c.1334A>T (p.Glu445Val) n.4755A>T c.1118A>T (p.Glu373Val) c.277+2207A>T (n.277+2207A>T) c.*1419A>T (n.*1419A>T) c.2375A>T (p.Glu792Val) | |
16 | g.89935786G>A | CA8256250 | TUBB3 | c.1335G>A (p.Glu445=) n.4756G>A c.1119G>A (p.Glu373=) c.277+2208G>A (n.277+2208G>A) c.*1420G>A (n.*1420G>A) c.2376G>A (p.Glu792=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935786G>C | CA397477269 | TUBB3 | c.1335G>C (p.Glu445Asp) n.4756G>C c.1119G>C (p.Glu373Asp) c.277+2208G>C (n.277+2208G>C) c.*1420G>C (n.*1420G>C) c.2376G>C (p.Glu792Asp) | |
16 | g.89935786G= | CA2242020908 | TUBB3 | c.1335G= (p.Glu445=) n.4756G= c.1119G= (p.Glu373=) c.277+2208G= (n.277+2208G=) c.*1420G= (n.*1420G=) c.2376G= (p.Glu792=) | |
16 | g.89935786G>T | CA397477268 | TUBB3 | c.1335G>T (p.Glu445Asp) n.4756G>T c.1119G>T (p.Glu373Asp) c.277+2208G>T (n.277+2208G>T) c.*1420G>T (n.*1420G>T) c.2376G>T (p.Glu792Asp) | gnomAD v4 |
16 | g.89935787G>A | CA8256251 | TUBB3 | c.1336G>A (p.Ala446Thr) n.4757G>A c.1120G>A (p.Ala374Thr) c.277+2209G>A (n.277+2209G>A) c.*1421G>A (n.*1421G>A) c.2377G>A (p.Ala793Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935787G>C | CA397477271 | TUBB3 | c.1336G>C (p.Ala446Pro) n.4757G>C c.1120G>C (p.Ala374Pro) c.277+2209G>C (n.277+2209G>C) c.*1421G>C (n.*1421G>C) c.2377G>C (p.Ala793Pro) | |
16 | g.89935787G= | CA2242020914 | TUBB3 | c.1336G= (p.Ala446=) n.4757G= c.1120G= (p.Ala374=) c.277+2209G= (n.277+2209G=) c.*1421G= (n.*1421G=) c.2377G= (p.Ala793=) | |
16 | g.89935787G>T | CA397477270 | TUBB3 | c.1336G>T (p.Ala446Ser) n.4757G>T c.1120G>T (p.Ala374Ser) c.277+2209G>T (n.277+2209G>T) c.*1421G>T (n.*1421G>T) c.2377G>T (p.Ala793Ser) | |
16 | g.89935788C>A | CA397477272 | TUBB3 | c.1337C>A (p.Ala446Asp) n.4758C>A c.1121C>A (p.Ala374Asp) c.277+2210C>A (n.277+2210C>A) c.*1422C>A (n.*1422C>A) c.2378C>A (p.Ala793Asp) | |
16 | g.89935788C>G | CA397477273 | TUBB3 | c.1337C>G (p.Ala446Gly) n.4758C>G c.1121C>G (p.Ala374Gly) c.277+2210C>G (n.277+2210C>G) c.*1422C>G (n.*1422C>G) c.2378C>G (p.Ala793Gly) | |
16 | g.89935788C>T | CA397477274 | TUBB3 | c.1337C>T (p.Ala446Val) n.4758C>T c.1121C>T (p.Ala374Val) c.277+2210C>T (n.277+2210C>T) c.*1422C>T (n.*1422C>T) c.2378C>T (p.Ala793Val) | ClinVar dbSNP |
16 | g.89935789C>A | CA497194563 | TUBB3 | c.1338C>A (p.Ala446=) n.4759C>A c.1122C>A (p.Ala374=) c.277+2211C>A (n.277+2211C>A) c.*1423C>A (n.*1423C>A) c.2379C>A (p.Ala793=) | |
16 | g.89935789C>G | CA497194564 | TUBB3 | c.1338C>G (p.Ala446=) n.4759C>G c.1122C>G (p.Ala374=) c.277+2211C>G (n.277+2211C>G) c.*1423C>G (n.*1423C>G) c.2379C>G (p.Ala793=) | |
16 | g.89935789C>T | CA497194562 | TUBB3 | c.1338C>T (p.Ala446=) n.4759C>T c.1122C>T (p.Ala374=) c.277+2211C>T (n.277+2211C>T) c.*1423C>T (n.*1423C>T) c.2379C>T (p.Ala793=) | |
16 | g.89935790C>A | CA397477275 | TUBB3 | c.1339C>A (p.Gln447Lys) n.4760C>A c.1123C>A (p.Gln375Lys) c.277+2212C>A (n.277+2212C>A) c.*1424C>A (n.*1424C>A) c.2380C>A (p.Gln794Lys) | |
16 | g.89935790C>G | CA397477276 | TUBB3 | c.1339C>G (p.Gln447Glu) n.4760C>G c.1123C>G (p.Gln375Glu) c.277+2212C>G (n.277+2212C>G) c.*1424C>G (n.*1424C>G) c.2380C>G (p.Gln794Glu) | |
16 | g.89935790C>T | CA397477277 | TUBB3 | c.1339C>T (p.Gln447Ter) n.4760C>T c.1123C>T (p.Gln375Ter) c.277+2212C>T (n.277+2212C>T) c.*1424C>T (n.*1424C>T) c.2380C>T (p.Gln794Ter) | |
16 | g.89935791A>C | CA397477278 | TUBB3 | c.1340A>C (p.Gln447Pro) n.4761A>C c.1124A>C (p.Gln375Pro) c.277+2213A>C (n.277+2213A>C) c.*1425A>C (n.*1425A>C) c.2381A>C (p.Gln794Pro) | |
16 | g.89935791A>G | CA397477279 | TUBB3 | c.1340A>G (p.Gln447Arg) n.4761A>G c.1124A>G (p.Gln375Arg) c.277+2213A>G (n.277+2213A>G) c.*1425A>G (n.*1425A>G) c.2381A>G (p.Gln794Arg) | gnomAD v4 |
16 | g.89935791A>T | CA397477280 | TUBB3 | c.1340A>T (p.Gln447Leu) n.4761A>T c.1124A>T (p.Gln375Leu) c.277+2213A>T (n.277+2213A>T) c.*1425A>T (n.*1425A>T) c.2381A>T (p.Gln794Leu) | |
16 | g.89935792G>A | CA497194568 | TUBB3 | c.1341G>A (p.Gln447=) n.4762G>A c.1125G>A (p.Gln375=) c.277+2214G>A (n.277+2214G>A) c.*1426G>A (n.*1426G>A) c.2382G>A (p.Gln794=) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.89935792G>C | CA397477281 | TUBB3 | c.1341G>C (p.Gln447His) n.4762G>C c.1125G>C (p.Gln375His) c.277+2214G>C (n.277+2214G>C) c.*1426G>C (n.*1426G>C) c.2382G>C (p.Gln794His) | gnomAD v4 |
16 | g.89935792G= | CA2242020919 | TUBB3 | c.1341G= (p.Gln447=) n.4762G= c.1125G= (p.Gln375=) c.277+2214G= (n.277+2214G=) c.*1426G= (n.*1426G=) c.2382G= (p.Gln794=) | |
16 | g.89935792G>T | CA397477282 | TUBB3 | c.1341G>T (p.Gln447His) n.4762G>T c.1125G>T (p.Gln375His) c.277+2214G>T (n.277+2214G>T) c.*1426G>T (n.*1426G>T) c.2382G>T (p.Gln794His) | |
16 | g.89935793G>A | CA397477285 | TUBB3 | c.1342G>A (p.Gly448Ser) n.4763G>A c.1126G>A (p.Gly376Ser) c.277+2215G>A (n.277+2215G>A) c.*1427G>A (n.*1427G>A) c.2383G>A (p.Gly795Ser) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
16 | g.89935793G>C | CA397477283 | TUBB3 | c.1342G>C (p.Gly448Arg) n.4763G>C c.1126G>C (p.Gly376Arg) c.277+2215G>C (n.277+2215G>C) c.*1427G>C (n.*1427G>C) c.2383G>C (p.Gly795Arg) | |
16 | g.89935793G= | CA2242020921 | TUBB3 | c.1342G= (p.Gly448=) n.4763G= c.1126G= (p.Gly376=) c.277+2215G= (n.277+2215G=) c.*1427G= (n.*1427G=) c.2383G= (p.Gly795=) | |
16 | g.89935793G>T | CA397477284 | TUBB3 | c.1342G>T (p.Gly448Cys) n.4763G>T c.1126G>T (p.Gly376Cys) c.277+2215G>T (n.277+2215G>T) c.*1427G>T (n.*1427G>T) c.2383G>T (p.Gly795Cys) | |
16 | g.89935794G>A | CA397477286 | TUBB3 | c.1343G>A (p.Gly448Asp) n.4764G>A c.1127G>A (p.Gly376Asp) c.277+2216G>A (n.277+2216G>A) c.*1428G>A (n.*1428G>A) c.2384G>A (p.Gly795Asp) | ClinVar gnomAD v4 |
16 | g.89935794G>C | CA397477287 | TUBB3 | c.1343G>C (p.Gly448Ala) n.4764G>C c.1127G>C (p.Gly376Ala) c.277+2216G>C (n.277+2216G>C) c.*1428G>C (n.*1428G>C) c.2384G>C (p.Gly795Ala) | |
16 | g.89935794G= | CA2242020923 | TUBB3 | c.1343G= (p.Gly448=) n.4764G= c.1127G= (p.Gly376=) c.277+2216G= (n.277+2216G=) c.*1428G= (n.*1428G=) c.2384G= (p.Gly795=) | |
16 | g.89935794G>T | CA397477288 | TUBB3 | c.1343G>T (p.Gly448Val) n.4764G>T c.1127G>T (p.Gly376Val) c.277+2216G>T (n.277+2216G>T) c.*1428G>T (n.*1428G>T) c.2384G>T (p.Gly795Val) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.89935795C>A | CA497194572 | TUBB3 | c.1344C>A (p.Gly448=) n.4765C>A c.1128C>A (p.Gly376=) c.277+2217C>A (n.277+2217C>A) c.*1429C>A (n.*1429C>A) c.2385C>A (p.Gly795=) | COSMIC |
16 | g.89935795C= | CA2242020925 | TUBB3 | c.1344C= (p.Gly448=) n.4765C= c.1128C= (p.Gly376=) c.277+2217C= (n.277+2217C=) c.*1429C= (n.*1429C=) c.2385C= (p.Gly795=) | |
16 | g.89935795C>G | CA497194573 | TUBB3 | c.1344C>G (p.Gly448=) n.4765C>G c.1128C>G (p.Gly376=) c.277+2217C>G (n.277+2217C>G) c.*1429C>G (n.*1429C>G) c.2385C>G (p.Gly795=) | |
16 | g.89935795C>T | CA8256252 | TUBB3 | c.1344C>T (p.Gly448=) n.4765C>T c.1128C>T (p.Gly376=) c.277+2217C>T (n.277+2217C>T) c.*1429C>T (n.*1429C>T) c.2385C>T (p.Gly795=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935796_89935798dup | CA2635070902 | TUBB3 | c.1345_1347dup (p.Pro449_Lys450insPro) n.4766_4768dup c.1129_1131dup (p.Pro377_Lys378insPro) c.277+2218_277+2220dup (n.277+2218_277+2220dup) c.*1430_*1432dup (n.*1430_*1432dup) c.2386_2388dup (p.Pro796_Lys797insPro) | gnomAD v4 |
16 | g.89935796C>A | CA397477289 | TUBB3 | c.1345C>A (p.Pro449Thr) n.4766C>A c.1129C>A (p.Pro377Thr) c.277+2218C>A (n.277+2218C>A) c.*1430C>A (n.*1430C>A) c.2386C>A (p.Pro796Thr) | |
16 | g.89935796C>G | CA397477290 | TUBB3 | c.1345C>G (p.Pro449Ala) n.4766C>G c.1129C>G (p.Pro377Ala) c.277+2218C>G (n.277+2218C>G) c.*1430C>G (n.*1430C>G) c.2386C>G (p.Pro796Ala) | gnomAD v4 |
16 | g.89935796C>T | CA397477291 | TUBB3 | c.1345C>T (p.Pro449Ser) n.4766C>T c.1129C>T (p.Pro377Ser) c.277+2218C>T (n.277+2218C>T) c.*1430C>T (n.*1430C>T) c.2386C>T (p.Pro796Ser) | |
16 | g.89935797C>A | CA397477292 | TUBB3 | c.1346C>A (p.Pro449His) n.4767C>A c.1130C>A (p.Pro377His) c.277+2219C>A (n.277+2219C>A) c.*1431C>A (n.*1431C>A) c.2387C>A (p.Pro796His) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935797C= | CA2242020929 | TUBB3 | c.1346C= (p.Pro449=) n.4767C= c.1130C= (p.Pro377=) c.277+2219C= (n.277+2219C=) c.*1431C= (n.*1431C=) c.2387C= (p.Pro796=) | |
16 | g.89935797C>G | CA397477293 | TUBB3 | c.1346C>G (p.Pro449Arg) n.4767C>G c.1130C>G (p.Pro377Arg) c.277+2219C>G (n.277+2219C>G) c.*1431C>G (n.*1431C>G) c.2387C>G (p.Pro796Arg) | |
16 | g.89935797C>T | CA397477294 | TUBB3 | c.1346C>T (p.Pro449Leu) n.4767C>T c.1130C>T (p.Pro377Leu) c.277+2219C>T (n.277+2219C>T) c.*1431C>T (n.*1431C>T) c.2387C>T (p.Pro796Leu) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.89935798C>A | CA497194577 | TUBB3 | c.1347C>A (p.Pro449=) n.4768C>A c.1131C>A (p.Pro377=) c.277+2220C>A (n.277+2220C>A) c.*1432C>A (n.*1432C>A) c.2388C>A (p.Pro796=) | |
16 | g.89935798C>G | CA497194578 | TUBB3 | c.1347C>G (p.Pro449=) n.4768C>G c.1131C>G (p.Pro377=) c.277+2220C>G (n.277+2220C>G) c.*1432C>G (n.*1432C>G) c.2388C>G (p.Pro796=) | |
16 | g.89935798C>T | CA497194579 | TUBB3 | c.1347C>T (p.Pro449=) n.4768C>T c.1131C>T (p.Pro377=) c.277+2220C>T (n.277+2220C>T) c.*1432C>T (n.*1432C>T) c.2388C>T (p.Pro796=) | |
16 | g.89935799A>C | CA397477296 | TUBB3 | c.1348A>C (p.Lys450Gln) n.4769A>C c.1132A>C (p.Lys378Gln) c.277+2221A>C (n.277+2221A>C) c.*1433A>C (n.*1433A>C) c.2389A>C (p.Lys797Gln) | |
16 | g.89935799A>G | CA397477297 | TUBB3 | c.1348A>G (p.Lys450Glu) n.4769A>G c.1132A>G (p.Lys378Glu) c.277+2221A>G (n.277+2221A>G) c.*1433A>G (n.*1433A>G) c.2389A>G (p.Lys797Glu) | |
16 | g.89935799A>T | CA397477295 | TUBB3 | c.1348A>T (p.Lys450Ter) n.4769A>T c.1132A>T (p.Lys378Ter) c.277+2221A>T (n.277+2221A>T) c.*1433A>T (n.*1433A>T) c.2389A>T (p.Lys797Ter) |