Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.89935196G>A | CA397475243 | TUBB3 | c.745G>A (p.Asp249Asn) n.4166G>A c.529G>A (p.Asp177Asn) c.277+1618G>A (n.277+1618G>A) c.*830G>A (n.*830G>A) c.1786G>A (p.Asp596Asn) | |
16 | g.89935196G>C | CA397475244 | TUBB3 | c.745G>C (p.Asp249His) n.4166G>C c.529G>C (p.Asp177His) c.277+1618G>C (n.277+1618G>C) c.*830G>C (n.*830G>C) c.1786G>C (p.Asp596His) | |
16 | g.89935196G>T | CA397475245 | TUBB3 | c.745G>T (p.Asp249Tyr) n.4166G>T c.529G>T (p.Asp177Tyr) c.277+1618G>T (n.277+1618G>T) c.*830G>T (n.*830G>T) c.1786G>T (p.Asp596Tyr) | |
16 | g.89935197A>C | CA397475246 | TUBB3 | c.746A>C (p.Asp249Ala) n.4167A>C c.530A>C (p.Asp177Ala) c.277+1619A>C (n.277+1619A>C) c.*831A>C (n.*831A>C) c.1787A>C (p.Asp596Ala) | |
16 | g.89935197A>G | CA397475247 | TUBB3 | c.746A>G (p.Asp249Gly) n.4167A>G c.530A>G (p.Asp177Gly) c.277+1619A>G (n.277+1619A>G) c.*831A>G (n.*831A>G) c.1787A>G (p.Asp596Gly) | |
16 | g.89935197A>T | CA397475248 | TUBB3 | c.746A>T (p.Asp249Val) n.4167A>T c.530A>T (p.Asp177Val) c.277+1619A>T (n.277+1619A>T) c.*831A>T (n.*831A>T) c.1787A>T (p.Asp596Val) | |
16 | g.89935198C>A | CA397475249 | TUBB3 | c.747C>A (p.Asp249Glu) n.4168C>A c.531C>A (p.Asp177Glu) c.277+1620C>A (n.277+1620C>A) c.*832C>A (n.*832C>A) c.1788C>A (p.Asp596Glu) | |
16 | g.89935198C= | CA2242020056 | TUBB3 | c.747C= (p.Asp249=) n.4168C= c.531C= (p.Asp177=) c.277+1620C= (n.277+1620C=) c.*832C= (n.*832C=) c.1788C= (p.Asp596=) | |
16 | g.89935198C>G | CA397475250 | TUBB3 | c.747C>G (p.Asp249Glu) n.4168C>G c.531C>G (p.Asp177Glu) c.277+1620C>G (n.277+1620C>G) c.*832C>G (n.*832C>G) c.1788C>G (p.Asp596Glu) | |
16 | g.89935198C>T | CA497381186 | TUBB3 | c.747C>T (p.Asp249=) n.4168C>T c.531C>T (p.Asp177=) c.277+1620C>T (n.277+1620C>T) c.*832C>T (n.*832C>T) c.1788C>T (p.Asp596=) | dbSNP |
16 | g.89935199C>A | CA397475251 | TUBB3 | c.748C>A (p.Leu250Met) n.4169C>A c.532C>A (p.Leu178Met) c.277+1621C>A (n.277+1621C>A) c.*833C>A (n.*833C>A) c.1789C>A (p.Leu597Met) | |
16 | g.89935199C>G | CA397475252 | TUBB3 | c.748C>G (p.Leu250Val) n.4169C>G c.532C>G (p.Leu178Val) c.277+1621C>G (n.277+1621C>G) c.*833C>G (n.*833C>G) c.1789C>G (p.Leu597Val) | |
16 | g.89935199C>T | CA497381188 | TUBB3 | c.748C>T (p.Leu250=) n.4169C>T c.532C>T (p.Leu178=) c.277+1621C>T (n.277+1621C>T) c.*833C>T (n.*833C>T) c.1789C>T (p.Leu597=) | |
16 | g.89935200T>A | CA397475253 | TUBB3 | c.749T>A (p.Leu250Gln) n.4170T>A c.533T>A (p.Leu178Gln) c.277+1622T>A (n.277+1622T>A) c.*834T>A (n.*834T>A) c.1790T>A (p.Leu597Gln) | |
16 | g.89935200T>C | CA397475254 | TUBB3 | c.749T>C (p.Leu250Pro) n.4170T>C c.533T>C (p.Leu178Pro) c.277+1622T>C (n.277+1622T>C) c.*834T>C (n.*834T>C) c.1790T>C (p.Leu597Pro) | gnomAD v4 |
16 | g.89935200T>G | CA397475255 | TUBB3 | c.749T>G (p.Leu250Arg) n.4170T>G c.533T>G (p.Leu178Arg) c.277+1622T>G (n.277+1622T>G) c.*834T>G (n.*834T>G) c.1790T>G (p.Leu597Arg) | |
16 | g.89935201G>A | CA8256160 | TUBB3 | c.750G>A (p.Leu250=) n.4171G>A c.534G>A (p.Leu178=) c.277+1623G>A (n.277+1623G>A) c.*835G>A (n.*835G>A) c.1791G>A (p.Leu597=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935201G>C | CA497381189 | TUBB3 | c.750G>C (p.Leu250=) n.4171G>C c.534G>C (p.Leu178=) c.277+1623G>C (n.277+1623G>C) c.*835G>C (n.*835G>C) c.1791G>C (p.Leu597=) | |
16 | g.89935201G= | CA2242020058 | TUBB3 | c.750G= (p.Leu250=) n.4171G= c.534G= (p.Leu178=) c.277+1623G= (n.277+1623G=) c.*835G= (n.*835G=) c.1791G= (p.Leu597=) | |
16 | g.89935201G>T | CA497381190 | TUBB3 | c.750G>T (p.Leu250=) n.4171G>T c.534G>T (p.Leu178=) c.277+1623G>T (n.277+1623G>T) c.*835G>T (n.*835G>T) c.1791G>T (p.Leu597=) | |
16 | g.89935202C>A | CA397475256 | TUBB3 | c.751C>A (p.Arg251Ser) n.4172C>A c.535C>A (p.Arg179Ser) c.277+1624C>A (n.277+1624C>A) c.*836C>A (n.*836C>A) c.1792C>A (p.Arg598Ser) | |
16 | g.89935202C= | CA2242020062 | TUBB3 | c.751C= (p.Arg251=) n.4172C= c.535C= (p.Arg179=) c.277+1624C= (n.277+1624C=) c.*836C= (n.*836C=) c.1792C= (p.Arg598=) | |
16 | g.89935202C>G | CA397475257 | TUBB3 | c.751C>G (p.Arg251Gly) n.4172C>G c.535C>G (p.Arg179Gly) c.277+1624C>G (n.277+1624C>G) c.*836C>G (n.*836C>G) c.1792C>G (p.Arg598Gly) | |
16 | g.89935202C>T | CA397475258 | TUBB3 | c.751C>T (p.Arg251Cys) n.4172C>T c.535C>T (p.Arg179Cys) c.277+1624C>T (n.277+1624C>T) c.*836C>T (n.*836C>T) c.1792C>T (p.Arg598Cys) | dbSNP |
16 | g.89935203G>A | CA397475259 | TUBB3 | c.752G>A (p.Arg251His) n.4173G>A c.536G>A (p.Arg179His) c.277+1625G>A (n.277+1625G>A) c.*837G>A (n.*837G>A) c.1793G>A (p.Arg598His) | ClinVar dbSNP gnomAD v4 |
16 | g.89935203G>C | CA397475260 | TUBB3 | c.752G>C (p.Arg251Pro) n.4173G>C c.536G>C (p.Arg179Pro) c.277+1625G>C (n.277+1625G>C) c.*837G>C (n.*837G>C) c.1793G>C (p.Arg598Pro) | |
16 | g.89935203G>T | CA397475261 | TUBB3 | c.752G>T (p.Arg251Leu) n.4173G>T c.536G>T (p.Arg179Leu) c.277+1625G>T (n.277+1625G>T) c.*837G>T (n.*837G>T) c.1793G>T (p.Arg598Leu) | |
16 | g.89935204C>A | CA497381193 | TUBB3 | c.753C>A (p.Arg251=) n.4174C>A c.537C>A (p.Arg179=) c.277+1626C>A (n.277+1626C>A) c.*838C>A (n.*838C>A) c.1794C>A (p.Arg598=) | dbSNP |
16 | g.89935204C= | CA2242020065 | TUBB3 | c.753C= (p.Arg251=) n.4174C= c.537C= (p.Arg179=) c.277+1626C= (n.277+1626C=) c.*838C= (n.*838C=) c.1794C= (p.Arg598=) | |
16 | g.89935204C>G | CA286619113 | TUBB3 | c.753C>G (p.Arg251=) n.4174C>G c.537C>G (p.Arg179=) c.277+1626C>G (n.277+1626C>G) c.*838C>G (n.*838C>G) c.1794C>G (p.Arg598=) | dbSNP |
16 | g.89935204C>T | CA8256161 | TUBB3 | c.753C>T (p.Arg251=) n.4174C>T c.537C>T (p.Arg179=) c.277+1626C>T (n.277+1626C>T) c.*838C>T (n.*838C>T) c.1794C>T (p.Arg598=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935205A>C | CA397475264 | TUBB3 | c.754A>C (p.Lys252Gln) n.4175A>C c.538A>C (p.Lys180Gln) c.277+1627A>C (n.277+1627A>C) c.*839A>C (n.*839A>C) c.1795A>C (p.Lys599Gln) | |
16 | g.89935205A>G | CA397475263 | TUBB3 | c.754A>G (p.Lys252Glu) n.4175A>G c.538A>G (p.Lys180Glu) c.277+1627A>G (n.277+1627A>G) c.*839A>G (n.*839A>G) c.1795A>G (p.Lys599Glu) | |
16 | g.89935205A>T | CA397475262 | TUBB3 | c.754A>T (p.Lys252Ter) n.4175A>T c.538A>T (p.Lys180Ter) c.277+1627A>T (n.277+1627A>T) c.*839A>T (n.*839A>T) c.1795A>T (p.Lys599Ter) | |
16 | g.89935206A>C | CA397475265 | TUBB3 | c.755A>C (p.Lys252Thr) n.4176A>C c.539A>C (p.Lys180Thr) c.277+1628A>C (n.277+1628A>C) c.*840A>C (n.*840A>C) c.1796A>C (p.Lys599Thr) | |
16 | g.89935206A>G | CA397475266 | TUBB3 | c.755A>G (p.Lys252Arg) n.4176A>G c.539A>G (p.Lys180Arg) c.277+1628A>G (n.277+1628A>G) c.*840A>G (n.*840A>G) c.1796A>G (p.Lys599Arg) | |
16 | g.89935206A>T | CA397475267 | TUBB3 | c.755A>T (p.Lys252Met) n.4176A>T c.539A>T (p.Lys180Met) c.277+1628A>T (n.277+1628A>T) c.*840A>T (n.*840A>T) c.1796A>T (p.Lys599Met) | |
16 | g.89935207G>A | CA497381197 | TUBB3 | c.756G>A (p.Lys252=) n.4177G>A c.540G>A (p.Lys180=) c.277+1629G>A (n.277+1629G>A) c.*841G>A (n.*841G>A) c.1797G>A (p.Lys599=) | gnomAD v4 |
16 | g.89935207G>C | CA397475268 | TUBB3 | c.756G>C (p.Lys252Asn) n.4177G>C c.540G>C (p.Lys180Asn) c.277+1629G>C (n.277+1629G>C) c.*841G>C (n.*841G>C) c.1797G>C (p.Lys599Asn) | ClinVar |
16 | g.89935207G>T | CA397475269 | TUBB3 | c.756G>T (p.Lys252Asn) n.4177G>T c.540G>T (p.Lys180Asn) c.277+1629G>T (n.277+1629G>T) c.*841G>T (n.*841G>T) c.1797G>T (p.Lys599Asn) | |
16 | g.89935208C>A | CA397475270 | TUBB3 | c.757C>A (p.Leu253Met) n.4178C>A c.541C>A (p.Leu181Met) c.277+1630C>A (n.277+1630C>A) c.*842C>A (n.*842C>A) c.1798C>A (p.Leu600Met) | |
16 | g.89935208C= | CA2242020068 | TUBB3 | c.757C= (p.Leu253=) n.4178C= c.541C= (p.Leu181=) c.277+1630C= (n.277+1630C=) c.*842C= (n.*842C=) c.1798C= (p.Leu600=) | |
16 | g.89935208C>G | CA397475271 | TUBB3 | c.757C>G (p.Leu253Val) n.4178C>G c.541C>G (p.Leu181Val) c.277+1630C>G (n.277+1630C>G) c.*842C>G (n.*842C>G) c.1798C>G (p.Leu600Val) | |
16 | g.89935208C>T | CA497381200 | TUBB3 | c.757C>T (p.Leu253=) n.4178C>T c.541C>T (p.Leu181=) c.277+1630C>T (n.277+1630C>T) c.*842C>T (n.*842C>T) c.1798C>T (p.Leu600=) | dbSNP |
16 | g.89935209T>A | CA397475272 | TUBB3 | c.758T>A (p.Leu253Gln) n.4179T>A c.542T>A (p.Leu181Gln) c.277+1631T>A (n.277+1631T>A) c.*843T>A (n.*843T>A) c.1799T>A (p.Leu600Gln) | |
16 | g.89935209T>C | CA397475273 | TUBB3 | c.758T>C (p.Leu253Pro) n.4179T>C c.542T>C (p.Leu181Pro) c.277+1631T>C (n.277+1631T>C) c.*843T>C (n.*843T>C) c.1799T>C (p.Leu600Pro) | |
16 | g.89935209T>G | CA397475274 | TUBB3 | c.758T>G (p.Leu253Arg) n.4179T>G c.542T>G (p.Leu181Arg) c.277+1631T>G (n.277+1631T>G) c.*843T>G (n.*843T>G) c.1799T>G (p.Leu600Arg) | |
16 | g.89935210G>A | CA497381202 | TUBB3 | c.759G>A (p.Leu253=) n.4180G>A c.543G>A (p.Leu181=) c.277+1632G>A (n.277+1632G>A) c.*844G>A (n.*844G>A) c.1800G>A (p.Leu600=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935210G>C | CA497381205 | TUBB3 | c.759G>C (p.Leu253=) n.4180G>C c.543G>C (p.Leu181=) c.277+1632G>C (n.277+1632G>C) c.*844G>C (n.*844G>C) c.1800G>C (p.Leu600=) | |
16 | g.89935210G= | CA2242020072 | TUBB3 | c.759G= (p.Leu253=) n.4180G= c.543G= (p.Leu181=) c.277+1632G= (n.277+1632G=) c.*844G= (n.*844G=) c.1800G= (p.Leu600=) | |
16 | g.89935210G>T | CA497381203 | TUBB3 | c.759G>T (p.Leu253=) n.4180G>T c.543G>T (p.Leu181=) c.277+1632G>T (n.277+1632G>T) c.*844G>T (n.*844G>T) c.1800G>T (p.Leu600=) | |
16 | g.89935210_89935214del | CA2808106652 | TUBB3 | c.759_763del (p.Ala254GlnfsTer?) n.4180_4184del c.543_547del (p.Ala182GlnfsTer?) c.277+1632_277+1636del (n.277+1632_277+1636del) c.*844_*848del (n.*844_*848del) c.1800_1804del (p.Ala601GlnfsTer?) | |
16 | g.89935211G>A | CA397475275 | TUBB3 | c.760G>A (p.Ala254Thr) n.4181G>A c.544G>A (p.Ala182Thr) c.277+1633G>A (n.277+1633G>A) c.*845G>A (n.*845G>A) c.1801G>A (p.Ala601Thr) | dbSNP |
16 | g.89935211G>C | CA397475276 | TUBB3 | c.760G>C (p.Ala254Pro) n.4181G>C c.544G>C (p.Ala182Pro) c.277+1633G>C (n.277+1633G>C) c.*845G>C (n.*845G>C) c.1801G>C (p.Ala601Pro) | |
16 | g.89935211G>T | CA397475277 | TUBB3 | c.760G>T (p.Ala254Ser) n.4181G>T c.544G>T (p.Ala182Ser) c.277+1633G>T (n.277+1633G>T) c.*845G>T (n.*845G>T) c.1801G>T (p.Ala601Ser) | |
16 | g.89935212C>A | CA397475279 | TUBB3 | c.761C>A (p.Ala254Asp) n.4182C>A c.545C>A (p.Ala182Asp) c.277+1634C>A (n.277+1634C>A) c.*846C>A (n.*846C>A) c.1802C>A (p.Ala601Asp) | |
16 | g.89935212C>G | CA397475280 | TUBB3 | c.761C>G (p.Ala254Gly) n.4182C>G c.545C>G (p.Ala182Gly) c.277+1634C>G (n.277+1634C>G) c.*846C>G (n.*846C>G) c.1802C>G (p.Ala601Gly) | |
16 | g.89935212C>T | CA397475278 | TUBB3 | c.761C>T (p.Ala254Val) n.4182C>T c.545C>T (p.Ala182Val) c.277+1634C>T (n.277+1634C>T) c.*846C>T (n.*846C>T) c.1802C>T (p.Ala601Val) | |
16 | g.89935213C>A | CA497381208 | TUBB3 | c.762C>A (p.Ala254=) n.4183C>A c.546C>A (p.Ala182=) c.277+1635C>A (n.277+1635C>A) c.*847C>A (n.*847C>A) c.1803C>A (p.Ala601=) | dbSNP gnomAD v4 |
16 | g.89935213C= | CA2242020074 | TUBB3 | c.762C= (p.Ala254=) n.4183C= c.546C= (p.Ala182=) c.277+1635C= (n.277+1635C=) c.*847C= (n.*847C=) c.1803C= (p.Ala601=) | |
16 | g.89935213C>G | CA497381209 | TUBB3 | c.762C>G (p.Ala254=) n.4183C>G c.546C>G (p.Ala182=) c.277+1635C>G (n.277+1635C>G) c.*847C>G (n.*847C>G) c.1803C>G (p.Ala601=) | dbSNP |
16 | g.89935213C>T | CA8256162 | TUBB3 | c.762C>T (p.Ala254=) n.4183C>T c.546C>T (p.Ala182=) c.277+1635C>T (n.277+1635C>T) c.*847C>T (n.*847C>T) c.1803C>T (p.Ala601=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
16 | g.89935214G>A | CA16043005 | TUBB3 | c.763G>A (p.Val255Ile) n.4184G>A c.547G>A (p.Val183Ile) c.277+1636G>A (n.277+1636G>A) c.*848G>A (n.*848G>A) c.1804G>A (p.Val602Ile) | ClinVar dbSNP gnomAD v4 COSMIC |
16 | g.89935214G>C | CA397475281 | TUBB3 | c.763G>C (p.Val255Leu) n.4184G>C c.547G>C (p.Val183Leu) c.277+1636G>C (n.277+1636G>C) c.*848G>C (n.*848G>C) c.1804G>C (p.Val602Leu) | |
16 | g.89935214G= | CA2242020079 | TUBB3 | c.763G= (p.Val255=) n.4184G= c.547G= (p.Val183=) c.277+1636G= (n.277+1636G=) c.*848G= (n.*848G=) c.1804G= (p.Val602=) | |
16 | g.89935214G>T | CA397475282 | TUBB3 | c.763G>T (p.Val255Phe) n.4184G>T c.547G>T (p.Val183Phe) c.277+1636G>T (n.277+1636G>T) c.*848G>T (n.*848G>T) c.1804G>T (p.Val602Phe) | |
16 | g.89935215T>A | CA397475283 | TUBB3 | c.764T>A (p.Val255Asp) n.4185T>A c.548T>A (p.Val183Asp) c.277+1637T>A (n.277+1637T>A) c.*849T>A (n.*849T>A) c.1805T>A (p.Val602Asp) | |
16 | g.89935215T>C | CA397475284 | TUBB3 | c.764T>C (p.Val255Ala) n.4185T>C c.548T>C (p.Val183Ala) c.277+1637T>C (n.277+1637T>C) c.*849T>C (n.*849T>C) c.1805T>C (p.Val602Ala) | |
16 | g.89935215T>G | CA397475285 | TUBB3 | c.764T>G (p.Val255Gly) n.4185T>G c.548T>G (p.Val183Gly) c.277+1637T>G (n.277+1637T>G) c.*849T>G (n.*849T>G) c.1805T>G (p.Val602Gly) | |
16 | g.89935216C>A | CA497381214 | TUBB3 | c.765C>A (p.Val255=) n.4186C>A c.549C>A (p.Val183=) c.277+1638C>A (n.277+1638C>A) c.*850C>A (n.*850C>A) c.1806C>A (p.Val602=) | |
16 | g.89935216C= | CA2242020081 | TUBB3 | c.765C= (p.Val255=) n.4186C= c.549C= (p.Val183=) c.277+1638C= (n.277+1638C=) c.*850C= (n.*850C=) c.1806C= (p.Val602=) | |
16 | g.89935216C>G | CA497381215 | TUBB3 | c.765C>G (p.Val255=) n.4186C>G c.549C>G (p.Val183=) c.277+1638C>G (n.277+1638C>G) c.*850C>G (n.*850C>G) c.1806C>G (p.Val602=) | dbSNP |
16 | g.89935216C>T | CA497381216 | TUBB3 | c.765C>T (p.Val255=) n.4186C>T c.549C>T (p.Val183=) c.277+1638C>T (n.277+1638C>T) c.*850C>T (n.*850C>T) c.1806C>T (p.Val602=) | |
16 | g.89935217A= | CA2242020085 | TUBB3 | c.766A= (p.Asn256=) n.4187A= c.550A= (p.Asn184=) c.277+1639A= (n.277+1639A=) c.*851A= (n.*851A=) c.1807A= (p.Asn603=) | |
16 | g.89935217A>C | CA397475286 | TUBB3 | c.766A>C (p.Asn256His) n.4187A>C c.550A>C (p.Asn184His) c.277+1639A>C (n.277+1639A>C) c.*851A>C (n.*851A>C) c.1807A>C (p.Asn603His) | |
16 | g.89935217A>G | CA397475287 | TUBB3 | c.766A>G (p.Asn256Asp) n.4187A>G c.550A>G (p.Asn184Asp) c.277+1639A>G (n.277+1639A>G) c.*851A>G (n.*851A>G) c.1807A>G (p.Asn603Asp) | |
16 | g.89935217A>T | CA16620314 | TUBB3 | c.766A>T (p.Asn256Tyr) n.4187A>T c.550A>T (p.Asn184Tyr) c.277+1639A>T (n.277+1639A>T) c.*851A>T (n.*851A>T) c.1807A>T (p.Asn603Tyr) | ClinVar dbSNP |
16 | g.89935218A>C | CA397475288 | TUBB3 | c.767A>C (p.Asn256Thr) n.4188A>C c.551A>C (p.Asn184Thr) c.277+1640A>C (n.277+1640A>C) c.*852A>C (n.*852A>C) c.1808A>C (p.Asn603Thr) | |
16 | g.89935218A>G | CA397475289 | TUBB3 | c.767A>G (p.Asn256Ser) n.4188A>G c.551A>G (p.Asn184Ser) c.277+1640A>G (n.277+1640A>G) c.*852A>G (n.*852A>G) c.1808A>G (p.Asn603Ser) | gnomAD v4 |
16 | g.89935218A>T | CA397475290 | TUBB3 | c.767A>T (p.Asn256Ile) n.4188A>T c.551A>T (p.Asn184Ile) c.277+1640A>T (n.277+1640A>T) c.*852A>T (n.*852A>T) c.1808A>T (p.Asn603Ile) | |
16 | g.89935219C>A | CA397475291 | TUBB3 | c.768C>A (p.Asn256Lys) n.4189C>A c.552C>A (p.Asn184Lys) c.277+1641C>A (n.277+1641C>A) c.*853C>A (n.*853C>A) c.1809C>A (p.Asn603Lys) | |
16 | g.89935219C>G | CA397475292 | TUBB3 | c.768C>G (p.Asn256Lys) n.4189C>G c.552C>G (p.Asn184Lys) c.277+1641C>G (n.277+1641C>G) c.*853C>G (n.*853C>G) c.1809C>G (p.Asn603Lys) | |
16 | g.89935219C>T | CA497381222 | TUBB3 | c.768C>T (p.Asn256=) n.4189C>T c.552C>T (p.Asn184=) c.277+1641C>T (n.277+1641C>T) c.*853C>T (n.*853C>T) c.1809C>T (p.Asn603=) | |
16 | g.89935220A= | CA2242020089 | TUBB3 | c.769A= (p.Met257=) n.4190A= c.553A= (p.Met185=) c.277+1642A= (n.277+1642A=) c.*854A= (n.*854A=) c.1810A= (p.Met604=) | |
16 | g.89935220A>C | CA397475293 | TUBB3 | c.769A>C (p.Met257Leu) n.4190A>C c.553A>C (p.Met185Leu) c.277+1642A>C (n.277+1642A>C) c.*854A>C (n.*854A>C) c.1810A>C (p.Met604Leu) | |
16 | g.89935220A>G | CA397475294 | TUBB3 | c.769A>G (p.Met257Val) n.4190A>G c.553A>G (p.Met185Val) c.277+1642A>G (n.277+1642A>G) c.*854A>G (n.*854A>G) c.1810A>G (p.Met604Val) | |
16 | g.89935220A>T | CA397475295 | TUBB3 | c.769A>T (p.Met257Leu) n.4190A>T c.553A>T (p.Met185Leu) c.277+1642A>T (n.277+1642A>T) c.*854A>T (n.*854A>T) c.1810A>T (p.Met604Leu) | dbSNP |
16 | g.89935221T>A | CA397475296 | TUBB3 | c.770T>A (p.Met257Lys) n.4191T>A c.554T>A (p.Met185Lys) c.277+1643T>A (n.277+1643T>A) c.*855T>A (n.*855T>A) c.1811T>A (p.Met604Lys) | |
16 | g.89935221T>C | CA397475297 | TUBB3 | c.770T>C (p.Met257Thr) n.4191T>C c.554T>C (p.Met185Thr) c.277+1643T>C (n.277+1643T>C) c.*855T>C (n.*855T>C) c.1811T>C (p.Met604Thr) | |
16 | g.89935221T>G | CA397475298 | TUBB3 | c.770T>G (p.Met257Arg) n.4191T>G c.554T>G (p.Met185Arg) c.277+1643T>G (n.277+1643T>G) c.*855T>G (n.*855T>G) c.1811T>G (p.Met604Arg) | |
16 | g.89935222G>A | CA397475299 | TUBB3 | c.771G>A (p.Met257Ile) n.4192G>A c.555G>A (p.Met185Ile) c.277+1644G>A (n.277+1644G>A) c.*856G>A (n.*856G>A) c.1812G>A (p.Met604Ile) | |
16 | g.89935222G>C | CA397475300 | TUBB3 | c.771G>C (p.Met257Ile) n.4192G>C c.555G>C (p.Met185Ile) c.277+1644G>C (n.277+1644G>C) c.*856G>C (n.*856G>C) c.1812G>C (p.Met604Ile) | |
16 | g.89935222G>T | CA397475301 | TUBB3 | c.771G>T (p.Met257Ile) n.4192G>T c.555G>T (p.Met185Ile) c.277+1644G>T (n.277+1644G>T) c.*856G>T (n.*856G>T) c.1812G>T (p.Met604Ile) | |
16 | g.89935223G>A | CA397475302 | TUBB3 | c.772G>A (p.Val258Met) n.4193G>A c.556G>A (p.Val186Met) c.277+1645G>A (n.277+1645G>A) c.*857G>A (n.*857G>A) c.1813G>A (p.Val605Met) | |
16 | g.89935223G>C | CA397475303 | TUBB3 | c.772G>C (p.Val258Leu) n.4193G>C c.556G>C (p.Val186Leu) c.277+1645G>C (n.277+1645G>C) c.*857G>C (n.*857G>C) c.1813G>C (p.Val605Leu) | |
16 | g.89935223G>T | CA397475304 | TUBB3 | c.772G>T (p.Val258Leu) n.4193G>T c.556G>T (p.Val186Leu) c.277+1645G>T (n.277+1645G>T) c.*857G>T (n.*857G>T) c.1813G>T (p.Val605Leu) | |
16 | g.89935224T>A | CA397475306 | TUBB3 | c.773T>A (p.Val258Glu) n.4194T>A c.557T>A (p.Val186Glu) c.277+1646T>A (n.277+1646T>A) c.*858T>A (n.*858T>A) c.1814T>A (p.Val605Glu) | |
16 | g.89935224T>C | CA397475307 | TUBB3 | c.773T>C (p.Val258Ala) n.4194T>C c.557T>C (p.Val186Ala) c.277+1646T>C (n.277+1646T>C) c.*858T>C (n.*858T>C) c.1814T>C (p.Val605Ala) | |
16 | g.89935224T>G | CA397475305 | TUBB3 | c.773T>G (p.Val258Gly) n.4194T>G c.557T>G (p.Val186Gly) c.277+1646T>G (n.277+1646T>G) c.*858T>G (n.*858T>G) c.1814T>G (p.Val605Gly) | |
16 | g.89935225G>A | CA8256163 | TUBB3 | c.774G>A (p.Val258=) n.4195G>A c.558G>A (p.Val186=) c.277+1647G>A (n.277+1647G>A) c.*859G>A (n.*859G>A) c.1815G>A (p.Val605=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.89935225G>C | CA497381228 | TUBB3 | c.774G>C (p.Val258=) n.4195G>C c.558G>C (p.Val186=) c.277+1647G>C (n.277+1647G>C) c.*859G>C (n.*859G>C) c.1815G>C (p.Val605=) | |
16 | g.89935225G= | CA2242020090 | TUBB3 | c.774G= (p.Val258=) n.4195G= c.558G= (p.Val186=) c.277+1647G= (n.277+1647G=) c.*859G= (n.*859G=) c.1815G= (p.Val605=) | |
16 | g.89935225G>T | CA497381230 | TUBB3 | c.774G>T (p.Val258=) n.4195G>T c.558G>T (p.Val186=) c.277+1647G>T (n.277+1647G>T) c.*859G>T (n.*859G>T) c.1815G>T (p.Val605=) | COSMIC |
16 | g.89935226C>A | CA397475308 | TUBB3 | c.775C>A (p.Pro259Thr) n.4196C>A c.559C>A (p.Pro187Thr) c.277+1648C>A (n.277+1648C>A) c.*860C>A (n.*860C>A) c.1816C>A (p.Pro606Thr) | |
16 | g.89935226C>G | CA397475309 | TUBB3 | c.775C>G (p.Pro259Ala) n.4196C>G c.559C>G (p.Pro187Ala) c.277+1648C>G (n.277+1648C>G) c.*860C>G (n.*860C>G) c.1816C>G (p.Pro606Ala) | |
16 | g.89935226C>T | CA397475310 | TUBB3 | c.775C>T (p.Pro259Ser) n.4196C>T c.559C>T (p.Pro187Ser) c.277+1648C>T (n.277+1648C>T) c.*860C>T (n.*860C>T) c.1816C>T (p.Pro606Ser) | |
16 | g.89935228dup | CA2242020093 | TUBB3 | c.777dup (p.Phe260LeufsTer?) n.4198dup c.561dup (p.Phe188LeufsTer?) c.277+1650dup (n.277+1650dup) c.*862dup (n.*862dup) c.1818dup (p.Phe607LeufsTer?) | dbSNP |
16 | g.89935227C>A | CA397475311 | TUBB3 | c.776C>A (p.Pro259His) n.4197C>A c.560C>A (p.Pro187His) c.277+1649C>A (n.277+1649C>A) c.*861C>A (n.*861C>A) c.1817C>A (p.Pro606His) | |
16 | g.89935227C>G | CA397475312 | TUBB3 | c.776C>G (p.Pro259Arg) n.4197C>G c.560C>G (p.Pro187Arg) c.277+1649C>G (n.277+1649C>G) c.*861C>G (n.*861C>G) c.1817C>G (p.Pro606Arg) | |
16 | g.89935227C>T | CA397475313 | TUBB3 | c.776C>T (p.Pro259Leu) n.4197C>T c.560C>T (p.Pro187Leu) c.277+1649C>T (n.277+1649C>T) c.*861C>T (n.*861C>T) c.1817C>T (p.Pro606Leu) | |
16 | g.89935228C>A | CA497381235 | TUBB3 | c.777C>A (p.Pro259=) n.4198C>A c.561C>A (p.Pro187=) c.277+1650C>A (n.277+1650C>A) c.*862C>A (n.*862C>A) c.1818C>A (p.Pro606=) | |
16 | g.89935228C= | CA2242020095 | TUBB3 | c.777C= (p.Pro259=) n.4198C= c.561C= (p.Pro187=) c.277+1650C= (n.277+1650C=) c.*862C= (n.*862C=) c.1818C= (p.Pro606=) | |
16 | g.89935228C>G | CA497381236 | TUBB3 | c.777C>G (p.Pro259=) n.4198C>G c.561C>G (p.Pro187=) c.277+1650C>G (n.277+1650C>G) c.*862C>G (n.*862C>G) c.1818C>G (p.Pro606=) | |
16 | g.89935228C>T | CA497381237 | TUBB3 | c.777C>T (p.Pro259=) n.4198C>T c.561C>T (p.Pro187=) c.277+1650C>T (n.277+1650C>T) c.*862C>T (n.*862C>T) c.1818C>T (p.Pro606=) | dbSNP |
16 | g.89935229T>A | CA397475316 | TUBB3 | c.778T>A (p.Phe260Ile) n.4199T>A c.562T>A (p.Phe188Ile) c.277+1651T>A (n.277+1651T>A) c.*863T>A (n.*863T>A) c.1819T>A (p.Phe607Ile) | |
16 | g.89935229T>C | CA397475314 | TUBB3 | c.778T>C (p.Phe260Leu) n.4199T>C c.562T>C (p.Phe188Leu) c.277+1651T>C (n.277+1651T>C) c.*863T>C (n.*863T>C) c.1819T>C (p.Phe607Leu) | |
16 | g.89935229T>G | CA397475315 | TUBB3 | c.778T>G (p.Phe260Val) n.4199T>G c.562T>G (p.Phe188Val) c.277+1651T>G (n.277+1651T>G) c.*863T>G (n.*863T>G) c.1819T>G (p.Phe607Val) | |
16 | g.89935230T>A | CA397475317 | TUBB3 | c.779T>A (p.Phe260Tyr) n.4200T>A c.563T>A (p.Phe188Tyr) c.277+1652T>A (n.277+1652T>A) c.*864T>A (n.*864T>A) c.1820T>A (p.Phe607Tyr) | |
16 | g.89935230T>C | CA397475318 | TUBB3 | c.779T>C (p.Phe260Ser) n.4200T>C c.563T>C (p.Phe188Ser) c.277+1652T>C (n.277+1652T>C) c.*864T>C (n.*864T>C) c.1820T>C (p.Phe607Ser) | dbSNP |
16 | g.89935230T>G | CA397475319 | TUBB3 | c.779T>G (p.Phe260Cys) n.4200T>G c.563T>G (p.Phe188Cys) c.277+1652T>G (n.277+1652T>G) c.*864T>G (n.*864T>G) c.1820T>G (p.Phe607Cys) | gnomAD v4 |
16 | g.89935230T= | CA2242020098 | TUBB3 | c.779T= (p.Phe260=) n.4200T= c.563T= (p.Phe188=) c.277+1652T= (n.277+1652T=) c.*864T= (n.*864T=) c.1820T= (p.Phe607=) | |
16 | g.89935231C>A | CA397475320 | TUBB3 | c.780C>A (p.Phe260Leu) n.4201C>A c.564C>A (p.Phe188Leu) c.277+1653C>A (n.277+1653C>A) c.*865C>A (n.*865C>A) c.1821C>A (p.Phe607Leu) | |
16 | g.89935231C= | CA2242020101 | TUBB3 | c.780C= (p.Phe260=) n.4201C= c.564C= (p.Phe188=) c.277+1653C= (n.277+1653C=) c.*865C= (n.*865C=) c.1821C= (p.Phe607=) | |
16 | g.89935231C>G | CA397475321 | TUBB3 | c.780C>G (p.Phe260Leu) n.4201C>G c.564C>G (p.Phe188Leu) c.277+1653C>G (n.277+1653C>G) c.*865C>G (n.*865C>G) c.1821C>G (p.Phe607Leu) | |
16 | g.89935231C>T | CA497381241 | TUBB3 | c.780C>T (p.Phe260=) n.4201C>T c.564C>T (p.Phe188=) c.277+1653C>T (n.277+1653C>T) c.*865C>T (n.*865C>T) c.1821C>T (p.Phe607=) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.89935232C>A | CA397475324 | TUBB3 | c.781C>A (p.Pro261Thr) n.4202C>A c.565C>A (p.Pro189Thr) c.277+1654C>A (n.277+1654C>A) c.*866C>A (n.*866C>A) c.1822C>A (p.Pro608Thr) | |
16 | g.89935232C>G | CA397475322 | TUBB3 | c.781C>G (p.Pro261Ala) n.4202C>G c.565C>G (p.Pro189Ala) c.277+1654C>G (n.277+1654C>G) c.*866C>G (n.*866C>G) c.1822C>G (p.Pro608Ala) | |
16 | g.89935232C>T | CA397475323 | TUBB3 | c.781C>T (p.Pro261Ser) n.4202C>T c.565C>T (p.Pro189Ser) c.277+1654C>T (n.277+1654C>T) c.*866C>T (n.*866C>T) c.1822C>T (p.Pro608Ser) | COSMIC |
16 | g.89935233C>A | CA397475325 | TUBB3 | c.782C>A (p.Pro261Gln) n.4203C>A c.566C>A (p.Pro189Gln) c.277+1655C>A (n.277+1655C>A) c.*867C>A (n.*867C>A) c.1823C>A (p.Pro608Gln) | |
16 | g.89935233C= | CA2242020103 | TUBB3 | c.782C= (p.Pro261=) n.4203C= c.566C= (p.Pro189=) c.277+1655C= (n.277+1655C=) c.*867C= (n.*867C=) c.1823C= (p.Pro608=) | |
16 | g.89935233C>G | CA397475326 | TUBB3 | c.782C>G (p.Pro261Arg) n.4203C>G c.566C>G (p.Pro189Arg) c.277+1655C>G (n.277+1655C>G) c.*867C>G (n.*867C>G) c.1823C>G (p.Pro608Arg) | |
16 | g.89935233C>T | CA397475327 | TUBB3 | c.782C>T (p.Pro261Leu) n.4203C>T c.566C>T (p.Pro189Leu) c.277+1655C>T (n.277+1655C>T) c.*867C>T (n.*867C>T) c.1823C>T (p.Pro608Leu) | dbSNP gnomAD v4 |
16 | g.89935234G>A | CA8256164 | TUBB3 | c.783G>A (p.Pro261=) n.4204G>A c.567G>A (p.Pro189=) c.277+1656G>A (n.277+1656G>A) c.*868G>A (n.*868G>A) c.1824G>A (p.Pro608=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
16 | g.89935234G>C | CA497381246 | TUBB3 | c.783G>C (p.Pro261=) n.4204G>C c.567G>C (p.Pro189=) c.277+1656G>C (n.277+1656G>C) c.*868G>C (n.*868G>C) c.1824G>C (p.Pro608=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935234G= | CA2242020111 | TUBB3 | c.783G= (p.Pro261=) n.4204G= c.567G= (p.Pro189=) c.277+1656G= (n.277+1656G=) c.*868G= (n.*868G=) c.1824G= (p.Pro608=) | |
16 | g.89935234G>T | CA497381248 | TUBB3 | c.783G>T (p.Pro261=) n.4204G>T c.567G>T (p.Pro189=) c.277+1656G>T (n.277+1656G>T) c.*868G>T (n.*868G>T) c.1824G>T (p.Pro608=) | dbSNP |
16 | g.89935235C>A | CA397475329 | TUBB3 | c.784C>A (p.Arg262Ser) n.4205C>A c.568C>A (p.Arg190Ser) c.277+1657C>A (n.277+1657C>A) c.*869C>A (n.*869C>A) c.568C>A c.1825C>A (p.Arg609Ser) | |
16 | g.89935235C= | CA2242020115 | TUBB3 | c.784C= (p.Arg262=) n.4205C= c.568C= (p.Arg190=) c.277+1657C= (n.277+1657C=) c.*869C= (n.*869C=) c.568C= c.1825C= (p.Arg609=) | |
16 | g.89935235C>G | CA397475330 | TUBB3 | c.784C>G (p.Arg262Gly) n.4205C>G c.568C>G (p.Arg190Gly) c.277+1657C>G (n.277+1657C>G) c.*869C>G (n.*869C>G) c.568C>G c.1825C>G (p.Arg609Gly) | |
16 | g.89935235C>T | CA340618 | TUBB3 | c.784C>T (p.Arg262Cys) n.4205C>T c.568C>T (p.Arg190Cys) c.277+1657C>T (n.277+1657C>T) c.*869C>T (n.*869C>T) c.568C>T c.1825C>T (p.Arg609Cys) | ClinVar dbSNP gnomAD v4 |
16 | g.89935236G>A | CA347962 | TUBB3 | c.785G>A (p.Arg262His) n.4206G>A c.569G>A (p.Arg190His) c.277+1658G>A (n.277+1658G>A) c.*870G>A (n.*870G>A) c.1826G>A (p.Arg609His) | ClinVar dbSNP |
16 | g.89935236G>C | CA397475332 | TUBB3 | c.785G>C (p.Arg262Pro) n.4206G>C c.569G>C (p.Arg190Pro) c.277+1658G>C (n.277+1658G>C) c.*870G>C (n.*870G>C) c.1826G>C (p.Arg609Pro) | |
16 | g.89935236G= | CA2242020128 | TUBB3 | c.785G= (p.Arg262=) n.4206G= c.569G= (p.Arg190=) c.277+1658G= (n.277+1658G=) c.*870G= (n.*870G=) c.1826G= (p.Arg609=) | |
16 | g.89935236G>T | CA397475333 | TUBB3 | c.785G>T (p.Arg262Leu) n.4206G>T c.569G>T (p.Arg190Leu) c.277+1658G>T (n.277+1658G>T) c.*870G>T (n.*870G>T) c.1826G>T (p.Arg609Leu) | |
16 | g.89935237C>A | CA497381255 | TUBB3 | c.786C>A (p.Arg262=) n.4207C>A c.570C>A (p.Arg190=) c.277+1659C>A (n.277+1659C>A) c.*871C>A (n.*871C>A) c.1827C>A (p.Arg609=) | |
16 | g.89935237C= | CA2242020132 | TUBB3 | c.786C= (p.Arg262=) n.4207C= c.570C= (p.Arg190=) c.277+1659C= (n.277+1659C=) c.*871C= (n.*871C=) c.1827C= (p.Arg609=) | |
16 | g.89935237C>G | CA497381258 | TUBB3 | c.786C>G (p.Arg262=) n.4207C>G c.570C>G (p.Arg190=) c.277+1659C>G (n.277+1659C>G) c.*871C>G (n.*871C>G) c.1827C>G (p.Arg609=) | |
16 | g.89935237C>T | CA497381256 | TUBB3 | c.786C>T (p.Arg262=) n.4207C>T c.570C>T (p.Arg190=) c.277+1659C>T (n.277+1659C>T) c.*871C>T (n.*871C>T) c.1827C>T (p.Arg609=) | dbSNP |
16 | g.89935238C>A | CA397475334 | TUBB3 | c.787C>A (p.Leu263Met) n.4208C>A c.571C>A (p.Leu191Met) c.277+1660C>A (n.277+1660C>A) c.*872C>A (n.*872C>A) c.1828C>A (p.Leu610Met) | COSMIC |
16 | g.89935238C>G | CA397475335 | TUBB3 | c.787C>G (p.Leu263Val) n.4208C>G c.571C>G (p.Leu191Val) c.277+1660C>G (n.277+1660C>G) c.*872C>G (n.*872C>G) c.1828C>G (p.Leu610Val) | COSMIC |
16 | g.89935238C>T | CA497381259 | TUBB3 | c.787C>T (p.Leu263=) n.4208C>T c.571C>T (p.Leu191=) c.277+1660C>T (n.277+1660C>T) c.*872C>T (n.*872C>T) c.1828C>T (p.Leu610=) | |
16 | g.89935239T>A | CA397475336 | TUBB3 | c.788T>A (p.Leu263Gln) n.4209T>A c.572T>A (p.Leu191Gln) c.277+1661T>A (n.277+1661T>A) c.*873T>A (n.*873T>A) c.1829T>A (p.Leu610Gln) | |
16 | g.89935239T>C | CA397475338 | TUBB3 | c.788T>C (p.Leu263Pro) n.4209T>C c.572T>C (p.Leu191Pro) c.277+1661T>C (n.277+1661T>C) c.*873T>C (n.*873T>C) c.1829T>C (p.Leu610Pro) | |
16 | g.89935239T>G | CA397475337 | TUBB3 | c.788T>G (p.Leu263Arg) n.4209T>G c.572T>G (p.Leu191Arg) c.277+1661T>G (n.277+1661T>G) c.*873T>G (n.*873T>G) c.1829T>G (p.Leu610Arg) | |
16 | g.89935240G>A | CA497381262 | TUBB3 | c.789G>A (p.Leu263=) n.4210G>A c.573G>A (p.Leu191=) c.277+1662G>A (n.277+1662G>A) c.*874G>A (n.*874G>A) c.1830G>A (p.Leu610=) | |
16 | g.89935240G>C | CA497381263 | TUBB3 | c.789G>C (p.Leu263=) n.4210G>C c.573G>C (p.Leu191=) c.277+1662G>C (n.277+1662G>C) c.*874G>C (n.*874G>C) c.1830G>C (p.Leu610=) | gnomAD v4 |
16 | g.89935240G>T | CA497381265 | TUBB3 | c.789G>T (p.Leu263=) n.4210G>T c.573G>T (p.Leu191=) c.277+1662G>T (n.277+1662G>T) c.*874G>T (n.*874G>T) c.1830G>T (p.Leu610=) | |
16 | g.89935241C>A | CA397475339 | TUBB3 | c.790C>A (p.His264Asn) n.4211C>A c.574C>A (p.His192Asn) c.277+1663C>A (n.277+1663C>A) c.*875C>A (n.*875C>A) c.1831C>A (p.His611Asn) | |
16 | g.89935241C>G | CA397475341 | TUBB3 | c.790C>G (p.His264Asp) n.4211C>G c.574C>G (p.His192Asp) c.277+1663C>G (n.277+1663C>G) c.*875C>G (n.*875C>G) c.1831C>G (p.His611Asp) | |
16 | g.89935241C>T | CA397475343 | TUBB3 | c.790C>T (p.His264Tyr) n.4211C>T c.574C>T (p.His192Tyr) c.277+1663C>T (n.277+1663C>T) c.*875C>T (n.*875C>T) c.1831C>T (p.His611Tyr) | |
16 | g.89935242A= | CA2242020135 | TUBB3 | c.791A= (p.His264=) n.4212A= c.575A= (p.His192=) c.277+1664A= (n.277+1664A=) c.*876A= (n.*876A=) c.1832A= (p.His611=) | |
16 | g.89935242A>C | CA397475344 | TUBB3 | c.791A>C (p.His264Pro) n.4212A>C c.575A>C (p.His192Pro) c.277+1664A>C (n.277+1664A>C) c.*876A>C (n.*876A>C) c.1832A>C (p.His611Pro) | dbSNP |
16 | g.89935242A>G | CA397475345 | TUBB3 | c.791A>G (p.His264Arg) n.4212A>G c.575A>G (p.His192Arg) c.277+1664A>G (n.277+1664A>G) c.*876A>G (n.*876A>G) c.1832A>G (p.His611Arg) | |
16 | g.89935242A>T | CA397475346 | TUBB3 | c.791A>T (p.His264Leu) n.4212A>T c.575A>T (p.His192Leu) c.277+1664A>T (n.277+1664A>T) c.*876A>T (n.*876A>T) c.1832A>T (p.His611Leu) | |
16 | g.89935243C>A | CA397475348 | TUBB3 | c.792C>A (p.His264Gln) n.4213C>A c.576C>A (p.His192Gln) c.277+1665C>A (n.277+1665C>A) c.*877C>A (n.*877C>A) c.1833C>A (p.His611Gln) | |
16 | g.89935243C>G | CA397475349 | TUBB3 | c.792C>G (p.His264Gln) n.4213C>G c.576C>G (p.His192Gln) c.277+1665C>G (n.277+1665C>G) c.*877C>G (n.*877C>G) c.1833C>G (p.His611Gln) | |
16 | g.89935243C>T | CA497381267 | TUBB3 | c.792C>T (p.His264=) n.4213C>T c.576C>T (p.His192=) c.277+1665C>T (n.277+1665C>T) c.*877C>T (n.*877C>T) c.1833C>T (p.His611=) | |
16 | g.89935244T>A | CA397475351 | TUBB3 | c.793T>A (p.Phe265Ile) n.4214T>A c.577T>A (p.Phe193Ile) c.277+1666T>A (n.277+1666T>A) c.*878T>A (n.*878T>A) c.1834T>A (p.Phe612Ile) | |
16 | g.89935244T>C | CA397475353 | TUBB3 | c.793T>C (p.Phe265Leu) n.4214T>C c.577T>C (p.Phe193Leu) c.277+1666T>C (n.277+1666T>C) c.*878T>C (n.*878T>C) c.1834T>C (p.Phe612Leu) | |
16 | g.89935244T>G | CA397475354 | TUBB3 | c.793T>G (p.Phe265Val) n.4214T>G c.577T>G (p.Phe193Val) c.277+1666T>G (n.277+1666T>G) c.*878T>G (n.*878T>G) c.1834T>G (p.Phe612Val) | |
16 | g.89935245T>A | CA397475359 | TUBB3 | c.794T>A (p.Phe265Tyr) n.4215T>A c.578T>A (p.Phe193Tyr) c.277+1667T>A (n.277+1667T>A) c.*879T>A (n.*879T>A) c.1835T>A (p.Phe612Tyr) | |
16 | g.89935245T>C | CA397475358 | TUBB3 | c.794T>C (p.Phe265Ser) n.4215T>C c.578T>C (p.Phe193Ser) c.277+1667T>C (n.277+1667T>C) c.*879T>C (n.*879T>C) c.1835T>C (p.Phe612Ser) | |
16 | g.89935245T>G | CA397475356 | TUBB3 | c.794T>G (p.Phe265Cys) n.4215T>G c.578T>G (p.Phe193Cys) c.277+1667T>G (n.277+1667T>G) c.*879T>G (n.*879T>G) c.1835T>G (p.Phe612Cys) | dbSNP |
16 | g.89935245T= | CA2242020138 | TUBB3 | c.794T= (p.Phe265=) n.4215T= c.578T= (p.Phe193=) c.277+1667T= (n.277+1667T=) c.*879T= (n.*879T=) c.1835T= (p.Phe612=) | |
16 | g.89935246C>A | CA397475361 | TUBB3 | c.795C>A (p.Phe265Leu) n.4216C>A c.579C>A (p.Phe193Leu) c.277+1668C>A (n.277+1668C>A) c.*880C>A (n.*880C>A) c.1836C>A (p.Phe612Leu) | |
16 | g.89935246C>G | CA397475363 | TUBB3 | c.795C>G (p.Phe265Leu) n.4216C>G c.579C>G (p.Phe193Leu) c.277+1668C>G (n.277+1668C>G) c.*880C>G (n.*880C>G) c.1836C>G (p.Phe612Leu) | |
16 | g.89935246C>T | CA497381273 | TUBB3 | c.795C>T (p.Phe265=) n.4216C>T c.579C>T (p.Phe193=) c.277+1668C>T (n.277+1668C>T) c.*880C>T (n.*880C>T) c.1836C>T (p.Phe612=) | gnomAD v4 |
16 | g.89935247T>A | CA397475364 | TUBB3 | c.796T>A (p.Phe266Ile) n.4217T>A c.580T>A (p.Phe194Ile) c.277+1669T>A (n.277+1669T>A) c.*881T>A (n.*881T>A) c.1837T>A (p.Phe613Ile) | |
16 | g.89935247T>C | CA397475366 | TUBB3 | c.796T>C (p.Phe266Leu) n.4217T>C c.580T>C (p.Phe194Leu) c.277+1669T>C (n.277+1669T>C) c.*881T>C (n.*881T>C) c.1837T>C (p.Phe613Leu) | |
16 | g.89935247T>G | CA397475367 | TUBB3 | c.796T>G (p.Phe266Val) n.4217T>G c.580T>G (p.Phe194Val) c.277+1669T>G (n.277+1669T>G) c.*881T>G (n.*881T>G) c.1837T>G (p.Phe613Val) | |
16 | g.89935248T>A | CA397475369 | TUBB3 | c.797T>A (p.Phe266Tyr) n.4218T>A c.581T>A (p.Phe194Tyr) c.277+1670T>A (n.277+1670T>A) c.*882T>A (n.*882T>A) c.1838T>A (p.Phe613Tyr) | |
16 | g.89935248T>C | CA397475371 | TUBB3 | c.797T>C (p.Phe266Ser) n.4218T>C c.581T>C (p.Phe194Ser) c.277+1670T>C (n.277+1670T>C) c.*882T>C (n.*882T>C) c.1838T>C (p.Phe613Ser) | |
16 | g.89935248T>G | CA397475373 | TUBB3 | c.797T>G (p.Phe266Cys) n.4218T>G c.581T>G (p.Phe194Cys) c.277+1670T>G (n.277+1670T>G) c.*882T>G (n.*882T>G) c.1838T>G (p.Phe613Cys) | |
16 | g.89935249C>A | CA397475374 | TUBB3 | c.798C>A (p.Phe266Leu) n.4219C>A c.582C>A (p.Phe194Leu) c.277+1671C>A (n.277+1671C>A) c.*883C>A (n.*883C>A) c.1839C>A (p.Phe613Leu) | |
16 | g.89935249C= | CA2242020142 | TUBB3 | c.798C= (p.Phe266=) n.4219C= c.582C= (p.Phe194=) c.277+1671C= (n.277+1671C=) c.*883C= (n.*883C=) c.1839C= (p.Phe613=) | |
16 | g.89935249C>G | CA397475376 | TUBB3 | c.798C>G (p.Phe266Leu) n.4219C>G c.582C>G (p.Phe194Leu) c.277+1671C>G (n.277+1671C>G) c.*883C>G (n.*883C>G) c.1839C>G (p.Phe613Leu) | |
16 | g.89935249C>T | CA497381281 | TUBB3 | c.798C>T (p.Phe266=) n.4219C>T c.582C>T (p.Phe194=) c.277+1671C>T (n.277+1671C>T) c.*883C>T (n.*883C>T) c.1839C>T (p.Phe613=) | dbSNP gnomAD v4 |
16 | g.89935250A>C | CA397475378 | TUBB3 | c.799A>C (p.Met267Leu) n.4220A>C c.583A>C (p.Met195Leu) c.277+1672A>C (n.277+1672A>C) c.*884A>C (n.*884A>C) c.1840A>C (p.Met614Leu) | |
16 | g.89935250A>G | CA397475380 | TUBB3 | c.799A>G (p.Met267Val) n.4220A>G c.583A>G (p.Met195Val) c.277+1672A>G (n.277+1672A>G) c.*884A>G (n.*884A>G) c.1840A>G (p.Met614Val) | |
16 | g.89935250A>T | CA397475381 | TUBB3 | c.799A>T (p.Met267Leu) n.4220A>T c.583A>T (p.Met195Leu) c.277+1672A>T (n.277+1672A>T) c.*884A>T (n.*884A>T) c.1840A>T (p.Met614Leu) | |
16 | g.89935251T>A | CA397475384 | TUBB3 | c.800T>A (p.Met267Lys) n.4221T>A c.584T>A (p.Met195Lys) c.277+1673T>A (n.277+1673T>A) c.*885T>A (n.*885T>A) c.1841T>A (p.Met614Lys) | |
16 | g.89935251T>C | CA397475385 | TUBB3 | c.800T>C (p.Met267Thr) n.4221T>C c.584T>C (p.Met195Thr) c.277+1673T>C (n.277+1673T>C) c.*885T>C (n.*885T>C) c.1841T>C (p.Met614Thr) | gnomAD v4 |
16 | g.89935251T>G | CA397475383 | TUBB3 | c.800T>G (p.Met267Arg) n.4221T>G c.584T>G (p.Met195Arg) c.277+1673T>G (n.277+1673T>G) c.*885T>G (n.*885T>G) c.1841T>G (p.Met614Arg) | |
16 | g.89935252G>A | CA397475389 | TUBB3 | c.801G>A (p.Met267Ile) n.4222G>A c.585G>A (p.Met195Ile) c.277+1674G>A (n.277+1674G>A) c.*886G>A (n.*886G>A) c.1842G>A (p.Met614Ile) | ClinVar gnomAD v4 |
16 | g.89935252G>C | CA397475387 | TUBB3 | c.801G>C (p.Met267Ile) n.4222G>C c.585G>C (p.Met195Ile) c.277+1674G>C (n.277+1674G>C) c.*886G>C (n.*886G>C) c.1842G>C (p.Met614Ile) | |
16 | g.89935252G>T | CA397475388 | TUBB3 | c.801G>T (p.Met267Ile) n.4222G>T c.585G>T (p.Met195Ile) c.277+1674G>T (n.277+1674G>T) c.*886G>T (n.*886G>T) c.1842G>T (p.Met614Ile) | |
16 | g.89935253C>A | CA397475390 | TUBB3 | c.802C>A (p.Pro268Thr) n.4223C>A c.586C>A (p.Pro196Thr) c.277+1675C>A (n.277+1675C>A) c.*887C>A (n.*887C>A) c.1843C>A (p.Pro615Thr) | |
16 | g.89935253C>G | CA397475391 | TUBB3 | c.802C>G (p.Pro268Ala) n.4223C>G c.586C>G (p.Pro196Ala) c.277+1675C>G (n.277+1675C>G) c.*887C>G (n.*887C>G) c.1843C>G (p.Pro615Ala) | |
16 | g.89935253C>T | CA397475393 | TUBB3 | c.802C>T (p.Pro268Ser) n.4223C>T c.586C>T (p.Pro196Ser) c.277+1675C>T (n.277+1675C>T) c.*887C>T (n.*887C>T) c.1843C>T (p.Pro615Ser) | ClinVar |
16 | g.89935254C>A | CA397475395 | TUBB3 | c.803C>A (p.Pro268His) n.4224C>A c.587C>A (p.Pro196His) c.277+1676C>A (n.277+1676C>A) c.*888C>A (n.*888C>A) c.1844C>A (p.Pro615His) | |
16 | g.89935254C>G | CA397475397 | TUBB3 | c.803C>G (p.Pro268Arg) n.4224C>G c.587C>G (p.Pro196Arg) c.277+1676C>G (n.277+1676C>G) c.*888C>G (n.*888C>G) c.1844C>G (p.Pro615Arg) | |
16 | g.89935254C>T | CA397475398 | TUBB3 | c.803C>T (p.Pro268Leu) n.4224C>T c.587C>T (p.Pro196Leu) c.277+1676C>T (n.277+1676C>T) c.*888C>T (n.*888C>T) c.1844C>T (p.Pro615Leu) | |
16 | g.89935255C>A | CA497381291 | TUBB3 | c.804C>A (p.Pro268=) n.4225C>A c.588C>A (p.Pro196=) c.277+1677C>A (n.277+1677C>A) c.*889C>A (n.*889C>A) c.1845C>A (p.Pro615=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935255C= | CA2242020147 | TUBB3 | c.804C= (p.Pro268=) n.4225C= c.588C= (p.Pro196=) c.277+1677C= (n.277+1677C=) c.*889C= (n.*889C=) c.1845C= (p.Pro615=) | |
16 | g.89935255C>G | CA497381292 | TUBB3 | c.804C>G (p.Pro268=) n.4225C>G c.588C>G (p.Pro196=) c.277+1677C>G (n.277+1677C>G) c.*889C>G (n.*889C>G) c.1845C>G (p.Pro615=) | dbSNP gnomAD v4 |
16 | g.89935255C>T | CA8256165 | TUBB3 | c.804C>T (p.Pro268=) n.4225C>T c.588C>T (p.Pro196=) c.277+1677C>T (n.277+1677C>T) c.*889C>T (n.*889C>T) c.1845C>T (p.Pro615=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935256G>A | CA397475402 | TUBB3 | c.805G>A (p.Gly269Ser) n.4226G>A c.589G>A (p.Gly197Ser) c.277+1678G>A (n.277+1678G>A) c.*890G>A (n.*890G>A) c.1846G>A (p.Gly616Ser) | ClinVar dbSNP |
16 | g.89935256G>C | CA397475403 | TUBB3 | c.805G>C (p.Gly269Arg) n.4226G>C c.589G>C (p.Gly197Arg) c.277+1678G>C (n.277+1678G>C) c.*890G>C (n.*890G>C) c.1846G>C (p.Gly616Arg) | |
16 | g.89935256G>T | CA397475405 | TUBB3 | c.805G>T (p.Gly269Cys) n.4226G>T c.589G>T (p.Gly197Cys) c.277+1678G>T (n.277+1678G>T) c.*890G>T (n.*890G>T) c.1846G>T (p.Gly616Cys) | |
16 | g.89935256_89935262del | CA2808106671 | TUBB3 | c.805_811del (p.Gly269ProfsTer14) n.4226_4232del c.589_595del (p.Gly197ProfsTer14) c.277+1678_277+1684del (n.277+1678_277+1684del) c.*890_*896del (n.*890_*896del) c.1846_1852del (p.Gly616ProfsTer14) | |
16 | g.89935257G>A | CA397475406 | TUBB3 | c.806G>A (p.Gly269Asp) n.4227G>A c.590G>A (p.Gly197Asp) c.277+1679G>A (n.277+1679G>A) c.*891G>A (n.*891G>A) c.1847G>A (p.Gly616Asp) | |
16 | g.89935257G>C | CA397475407 | TUBB3 | c.806G>C (p.Gly269Ala) n.4227G>C c.590G>C (p.Gly197Ala) c.277+1679G>C (n.277+1679G>C) c.*891G>C (n.*891G>C) c.1847G>C (p.Gly616Ala) | |
16 | g.89935257G>T | CA397475408 | TUBB3 | c.806G>T (p.Gly269Val) n.4227G>T c.590G>T (p.Gly197Val) c.277+1679G>T (n.277+1679G>T) c.*891G>T (n.*891G>T) c.1847G>T (p.Gly616Val) | |
16 | g.89935258C>A | CA497381297 | TUBB3 | c.807C>A (p.Gly269=) n.4228C>A c.591C>A (p.Gly197=) c.277+1680C>A (n.277+1680C>A) c.*892C>A (n.*892C>A) c.1848C>A (p.Gly616=) | |
16 | g.89935258C>G | CA497381298 | TUBB3 | c.807C>G (p.Gly269=) n.4228C>G c.591C>G (p.Gly197=) c.277+1680C>G (n.277+1680C>G) c.*892C>G (n.*892C>G) c.1848C>G (p.Gly616=) | |
16 | g.89935258C>T | CA497381300 | TUBB3 | c.807C>T (p.Gly269=) n.4228C>T c.591C>T (p.Gly197=) c.277+1680C>T (n.277+1680C>T) c.*892C>T (n.*892C>T) c.1848C>T (p.Gly616=) | gnomAD v4 |
16 | g.89935259T>A | CA397475409 | TUBB3 | c.808T>A (p.Phe270Ile) n.4229T>A c.592T>A (p.Phe198Ile) c.277+1681T>A (n.277+1681T>A) c.*893T>A (n.*893T>A) c.1849T>A (p.Phe617Ile) | |
16 | g.89935259T>C | CA397475411 | TUBB3 | c.808T>C (p.Phe270Leu) n.4229T>C c.592T>C (p.Phe198Leu) c.277+1681T>C (n.277+1681T>C) c.*893T>C (n.*893T>C) c.1849T>C (p.Phe617Leu) | |
16 | g.89935259T>G | CA397475410 | TUBB3 | c.808T>G (p.Phe270Val) n.4229T>G c.592T>G (p.Phe198Val) c.277+1681T>G (n.277+1681T>G) c.*893T>G (n.*893T>G) c.1849T>G (p.Phe617Val) | |
16 | g.89935260T>A | CA397475412 | TUBB3 | c.809T>A (p.Phe270Tyr) n.4230T>A c.593T>A (p.Phe198Tyr) c.277+1682T>A (n.277+1682T>A) c.*894T>A (n.*894T>A) c.1850T>A (p.Phe617Tyr) | |
16 | g.89935260T>C | CA397475413 | TUBB3 | c.809T>C (p.Phe270Ser) n.4230T>C c.593T>C (p.Phe198Ser) c.277+1682T>C (n.277+1682T>C) c.*894T>C (n.*894T>C) c.1850T>C (p.Phe617Ser) | |
16 | g.89935260T>G | CA397475414 | TUBB3 | c.809T>G (p.Phe270Cys) n.4230T>G c.593T>G (p.Phe198Cys) c.277+1682T>G (n.277+1682T>G) c.*894T>G (n.*894T>G) c.1850T>G (p.Phe617Cys) | |
16 | g.89935261C>A | CA397475415 | TUBB3 | c.810C>A (p.Phe270Leu) n.4231C>A c.594C>A (p.Phe198Leu) c.277+1683C>A (n.277+1683C>A) c.*895C>A (n.*895C>A) c.1851C>A (p.Phe617Leu) | |
16 | g.89935261C= | CA2242020150 | TUBB3 | c.810C= (p.Phe270=) n.4231C= c.594C= (p.Phe198=) c.277+1683C= (n.277+1683C=) c.*895C= (n.*895C=) c.1851C= (p.Phe617=) | |
16 | g.89935261C>G | CA397475416 | TUBB3 | c.810C>G (p.Phe270Leu) n.4231C>G c.594C>G (p.Phe198Leu) c.277+1683C>G (n.277+1683C>G) c.*895C>G (n.*895C>G) c.1851C>G (p.Phe617Leu) | |
16 | g.89935261C>T | CA286619131 | TUBB3 | c.810C>T (p.Phe270=) n.4231C>T c.594C>T (p.Phe198=) c.277+1683C>T (n.277+1683C>T) c.*895C>T (n.*895C>T) c.1851C>T (p.Phe617=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
16 | g.89935262G>A | CA397475418 | TUBB3 | c.811G>A (p.Ala271Thr) n.4232G>A c.595G>A (p.Ala199Thr) c.277+1684G>A (n.277+1684G>A) c.*896G>A (n.*896G>A) c.1852G>A (p.Ala618Thr) | gnomAD v4 |
16 | g.89935262G>C | CA397475419 | TUBB3 | c.811G>C (p.Ala271Pro) n.4232G>C c.595G>C (p.Ala199Pro) c.277+1684G>C (n.277+1684G>C) c.*896G>C (n.*896G>C) c.1852G>C (p.Ala618Pro) | |
16 | g.89935262G>T | CA397475420 | TUBB3 | c.811G>T (p.Ala271Ser) n.4232G>T c.595G>T (p.Ala199Ser) c.277+1684G>T (n.277+1684G>T) c.*896G>T (n.*896G>T) c.1852G>T (p.Ala618Ser) | gnomAD v4 |
16 | g.89935263C>A | CA397475421 | TUBB3 | c.812C>A (p.Ala271Asp) n.4233C>A c.596C>A (p.Ala199Asp) c.277+1685C>A (n.277+1685C>A) c.*897C>A (n.*897C>A) c.1853C>A (p.Ala618Asp) | |
16 | g.89935263C>G | CA397475422 | TUBB3 | c.812C>G (p.Ala271Gly) n.4233C>G c.596C>G (p.Ala199Gly) c.277+1685C>G (n.277+1685C>G) c.*897C>G (n.*897C>G) c.1853C>G (p.Ala618Gly) | |
16 | g.89935263C>T | CA397475423 | TUBB3 | c.812C>T (p.Ala271Val) n.4233C>T c.596C>T (p.Ala199Val) c.277+1685C>T (n.277+1685C>T) c.*897C>T (n.*897C>T) c.1853C>T (p.Ala618Val) | |
16 | g.89935268dup | CA2635070895 | TUBB3 | c.817dup (p.Leu273ProfsTer?) n.4238dup c.601dup (p.Leu201ProfsTer?) c.277+1690dup (n.277+1690dup) c.*902dup (n.*902dup) c.1858dup (p.Leu620ProfsTer?) | gnomAD v4 |
16 | g.89935264C>A | CA497381307 | TUBB3 | c.813C>A (p.Ala271=) n.4234C>A c.597C>A (p.Ala199=) c.277+1686C>A (n.277+1686C>A) c.*898C>A (n.*898C>A) c.1854C>A (p.Ala618=) | |
16 | g.89935264C= | CA2242020155 | TUBB3 | c.813C= (p.Ala271=) n.4234C= c.597C= (p.Ala199=) c.277+1686C= (n.277+1686C=) c.*898C= (n.*898C=) c.1854C= (p.Ala618=) | |
16 | g.89935264C>G | CA497381308 | TUBB3 | c.813C>G (p.Ala271=) n.4234C>G c.597C>G (p.Ala199=) c.277+1686C>G (n.277+1686C>G) c.*898C>G (n.*898C>G) c.1854C>G (p.Ala618=) | |
16 | g.89935264C>T | CA8256166 | TUBB3 | c.813C>T (p.Ala271=) n.4234C>T c.597C>T (p.Ala199=) c.277+1686C>T (n.277+1686C>T) c.*898C>T (n.*898C>T) c.1854C>T (p.Ala618=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935265C>A | CA397475429 | TUBB3 | c.814C>A (p.Pro272Thr) n.4235C>A c.598C>A (p.Pro200Thr) c.277+1687C>A (n.277+1687C>A) c.*899C>A (n.*899C>A) c.1855C>A (p.Pro619Thr) | |
16 | g.89935265C>G | CA397475426 | TUBB3 | c.814C>G (p.Pro272Ala) n.4235C>G c.598C>G (p.Pro200Ala) c.277+1687C>G (n.277+1687C>G) c.*899C>G (n.*899C>G) c.1855C>G (p.Pro619Ala) | |
16 | g.89935265C>T | CA397475427 | TUBB3 | c.814C>T (p.Pro272Ser) n.4235C>T c.598C>T (p.Pro200Ser) c.277+1687C>T (n.277+1687C>T) c.*899C>T (n.*899C>T) c.1855C>T (p.Pro619Ser) | |
16 | g.89935266C>A | CA397475431 | TUBB3 | c.815C>A (p.Pro272His) n.4236C>A c.599C>A (p.Pro200His) c.277+1688C>A (n.277+1688C>A) c.*900C>A (n.*900C>A) c.1856C>A (p.Pro619His) | ClinVar dbSNP |
16 | g.89935266C>G | CA397475433 | TUBB3 | c.815C>G (p.Pro272Arg) n.4236C>G c.599C>G (p.Pro200Arg) c.277+1688C>G (n.277+1688C>G) c.*900C>G (n.*900C>G) c.1856C>G (p.Pro619Arg) | |
16 | g.89935266C>T | CA397475434 | TUBB3 | c.815C>T (p.Pro272Leu) n.4236C>T c.599C>T (p.Pro200Leu) c.277+1688C>T (n.277+1688C>T) c.*900C>T (n.*900C>T) c.1856C>T (p.Pro619Leu) | |
16 | g.89935267C>A | CA497381314 | TUBB3 | c.816C>A (p.Pro272=) n.4237C>A c.600C>A (p.Pro200=) c.277+1689C>A (n.277+1689C>A) c.*901C>A (n.*901C>A) c.1857C>A (p.Pro619=) | gnomAD v4 |
16 | g.89935267C= | CA2242020158 | TUBB3 | c.816C= (p.Pro272=) n.4237C= c.600C= (p.Pro200=) c.277+1689C= (n.277+1689C=) c.*901C= (n.*901C=) c.1857C= (p.Pro619=) | |
16 | g.89935267C>G | CA8256167 | TUBB3 | c.816C>G (p.Pro272=) n.4237C>G c.600C>G (p.Pro200=) c.277+1689C>G (n.277+1689C>G) c.*901C>G (n.*901C>G) c.1857C>G (p.Pro619=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935267C>T | CA497381316 | TUBB3 | c.816C>T (p.Pro272=) n.4237C>T c.600C>T (p.Pro200=) c.277+1689C>T (n.277+1689C>T) c.*901C>T (n.*901C>T) c.1857C>T (p.Pro619=) | |
16 | g.89935267_89935268insACACCAAACACACCCAA | CA2808106685 | TUBB3 | c.816_817insACACCAAACACACCCAA (p.Leu273ThrfsTer18) n.4237_4238insACACCAAACACACCCAA c.600_601insACACCAAACACACCCAA (p.Leu201ThrfsTer18) c.277+1689_277+1690insACACCAAACACACCCAA (n.277+1689_277+1690insACACCAAACACACCCAA) c.*901_*902insACACCAAACACACCCAA (n.*901_*902insACACCAAACACACCCAA) c.1857_1858insACACCAAACACACCCAA (p.Leu620ThrfsTer18) | |
16 | g.89935268C>A | CA397475440 | TUBB3 | c.817C>A (p.Leu273Ile) n.4238C>A c.601C>A (p.Leu201Ile) c.277+1690C>A (n.277+1690C>A) c.*902C>A (n.*902C>A) c.1858C>A (p.Leu620Ile) | |
16 | g.89935268C>G | CA397475438 | TUBB3 | c.817C>G (p.Leu273Val) n.4238C>G c.601C>G (p.Leu201Val) c.277+1690C>G (n.277+1690C>G) c.*902C>G (n.*902C>G) c.1858C>G (p.Leu620Val) | ClinVar COSMIC |
16 | g.89935268C>T | CA397475437 | TUBB3 | c.817C>T (p.Leu273Phe) n.4238C>T c.601C>T (p.Leu201Phe) c.277+1690C>T (n.277+1690C>T) c.*902C>T (n.*902C>T) c.1858C>T (p.Leu620Phe) | |
16 | g.89935269T>A | CA397475442 | TUBB3 | c.818T>A (p.Leu273His) n.4239T>A c.602T>A (p.Leu201His) c.277+1691T>A (n.277+1691T>A) c.*903T>A (n.*903T>A) c.1859T>A (p.Leu620His) | |
16 | g.89935269T>C | CA397475444 | TUBB3 | c.818T>C (p.Leu273Pro) n.4239T>C c.602T>C (p.Leu201Pro) c.277+1691T>C (n.277+1691T>C) c.*903T>C (n.*903T>C) c.1859T>C (p.Leu620Pro) | |
16 | g.89935269T>G | CA397475445 | TUBB3 | c.818T>G (p.Leu273Arg) n.4239T>G c.602T>G (p.Leu201Arg) c.277+1691T>G (n.277+1691T>G) c.*903T>G (n.*903T>G) c.1859T>G (p.Leu620Arg) | |
16 | g.89935270C>A | CA497381320 | TUBB3 | c.819C>A (p.Leu273=) n.4240C>A c.603C>A (p.Leu201=) c.277+1692C>A (n.277+1692C>A) c.*904C>A (n.*904C>A) c.1860C>A (p.Leu620=) | |
16 | g.89935270C>G | CA497381321 | TUBB3 | c.819C>G (p.Leu273=) n.4240C>G c.603C>G (p.Leu201=) c.277+1692C>G (n.277+1692C>G) c.*904C>G (n.*904C>G) c.1860C>G (p.Leu620=) | |
16 | g.89935270C>T | CA497381322 | TUBB3 | c.819C>T (p.Leu273=) n.4240C>T c.603C>T (p.Leu201=) c.277+1692C>T (n.277+1692C>T) c.*904C>T (n.*904C>T) c.1860C>T (p.Leu620=) | |
16 | g.89935271A>C | CA397475447 | TUBB3 | c.820A>C (p.Thr274Pro) n.4241A>C c.604A>C (p.Thr202Pro) c.277+1693A>C (n.277+1693A>C) c.*905A>C (n.*905A>C) c.1861A>C (p.Thr621Pro) | |
16 | g.89935271A>G | CA397475449 | TUBB3 | c.820A>G (p.Thr274Ala) n.4241A>G c.604A>G (p.Thr202Ala) c.277+1693A>G (n.277+1693A>G) c.*905A>G (n.*905A>G) c.1861A>G (p.Thr621Ala) | |
16 | g.89935271A>T | CA397475451 | TUBB3 | c.820A>T (p.Thr274Ser) n.4241A>T c.604A>T (p.Thr202Ser) c.277+1693A>T (n.277+1693A>T) c.*905A>T (n.*905A>T) c.1861A>T (p.Thr621Ser) | |
16 | g.89935272C>A | CA397475453 | TUBB3 | c.821C>A (p.Thr274Lys) n.4242C>A c.605C>A (p.Thr202Lys) c.277+1694C>A (n.277+1694C>A) c.*906C>A (n.*906C>A) c.1862C>A (p.Thr621Lys) | |
16 | g.89935272C= | CA2242020161 | TUBB3 | c.821C= (p.Thr274=) n.4242C= c.605C= (p.Thr202=) c.277+1694C= (n.277+1694C=) c.*906C= (n.*906C=) c.1862C= (p.Thr621=) | |
16 | g.89935272C>G | CA397475456 | TUBB3 | c.821C>G (p.Thr274Arg) n.4242C>G c.605C>G (p.Thr202Arg) c.277+1694C>G (n.277+1694C>G) c.*906C>G (n.*906C>G) c.1862C>G (p.Thr621Arg) | |
16 | g.89935272C>T | CA397475455 | TUBB3 | c.821C>T (p.Thr274Ile) n.4242C>T c.605C>T (p.Thr202Ile) c.277+1694C>T (n.277+1694C>T) c.*906C>T (n.*906C>T) c.1862C>T (p.Thr621Ile) | dbSNP gnomAD v4 |
16 | g.89935273A>C | CA497381327 | TUBB3 | c.822A>C (p.Thr274=) n.4243A>C c.606A>C (p.Thr202=) c.277+1695A>C (n.277+1695A>C) c.*907A>C (n.*907A>C) c.1863A>C (p.Thr621=) | |
16 | g.89935273A>G | CA497381326 | TUBB3 | c.822A>G (p.Thr274=) n.4243A>G c.606A>G (p.Thr202=) c.277+1695A>G (n.277+1695A>G) c.*907A>G (n.*907A>G) c.1863A>G (p.Thr621=) | |
16 | g.89935273A>T | CA497381325 | TUBB3 | c.822A>T (p.Thr274=) n.4243A>T c.606A>T (p.Thr202=) c.277+1695A>T (n.277+1695A>T) c.*907A>T (n.*907A>T) c.1863A>T (p.Thr621=) | |
16 | g.89935274G>A | CA397475457 | TUBB3 | c.823G>A (p.Ala275Thr) n.4244G>A c.607G>A (p.Ala203Thr) c.277+1696G>A (n.277+1696G>A) c.*908G>A (n.*908G>A) c.1864G>A (p.Ala622Thr) | |
16 | g.89935274G>C | CA397475459 | TUBB3 | c.823G>C (p.Ala275Pro) n.4244G>C c.607G>C (p.Ala203Pro) c.277+1696G>C (n.277+1696G>C) c.*908G>C (n.*908G>C) c.1864G>C (p.Ala622Pro) | |
16 | g.89935274G>T | CA397475460 | TUBB3 | c.823G>T (p.Ala275Ser) n.4244G>T c.607G>T (p.Ala203Ser) c.277+1696G>T (n.277+1696G>T) c.*908G>T (n.*908G>T) c.1864G>T (p.Ala622Ser) | |
16 | g.89935275C>A | CA397475461 | TUBB3 | c.824C>A (p.Ala275Asp) n.4245C>A c.608C>A (p.Ala203Asp) c.277+1697C>A (n.277+1697C>A) c.*909C>A (n.*909C>A) c.1865C>A (p.Ala622Asp) | |
16 | g.89935275C>G | CA397475463 | TUBB3 | c.824C>G (p.Ala275Gly) n.4245C>G c.608C>G (p.Ala203Gly) c.277+1697C>G (n.277+1697C>G) c.*909C>G (n.*909C>G) c.1865C>G (p.Ala622Gly) | |
16 | g.89935275C>T | CA397475464 | TUBB3 | c.824C>T (p.Ala275Val) n.4245C>T c.608C>T (p.Ala203Val) c.277+1697C>T (n.277+1697C>T) c.*909C>T (n.*909C>T) c.1865C>T (p.Ala622Val) | |
16 | g.89935276C>A | CA8256168 | TUBB3 | c.825C>A (p.Ala275=) n.4246C>A c.609C>A (p.Ala203=) c.277+1698C>A (n.277+1698C>A) c.*910C>A (n.*910C>A) c.1866C>A (p.Ala622=) | dbSNP ExAC gnomAD v2 |
16 | g.89935276C= | CA2242020164 | TUBB3 | c.825C= (p.Ala275=) n.4246C= c.609C= (p.Ala203=) c.277+1698C= (n.277+1698C=) c.*910C= (n.*910C=) c.1866C= (p.Ala622=) | |
16 | g.89935276C>G | CA497381329 | TUBB3 | c.825C>G (p.Ala275=) n.4246C>G c.609C>G (p.Ala203=) c.277+1698C>G (n.277+1698C>G) c.*910C>G (n.*910C>G) c.1866C>G (p.Ala622=) | gnomAD v4 |
16 | g.89935276C>T | CA497381330 | TUBB3 | c.825C>T (p.Ala275=) n.4246C>T c.609C>T (p.Ala203=) c.277+1698C>T (n.277+1698C>T) c.*910C>T (n.*910C>T) c.1866C>T (p.Ala622=) | |
16 | g.89935277C>A | CA497381331 | TUBB3 | c.826C>A (p.Arg276=) n.4247C>A c.610C>A (p.Arg204=) c.277+1699C>A (n.277+1699C>A) c.*911C>A (n.*911C>A) c.1867C>A (p.Arg623=) | |
16 | g.89935277C>G | CA397475467 | TUBB3 | c.826C>G (p.Arg276Gly) n.4247C>G c.610C>G (p.Arg204Gly) c.277+1699C>G (n.277+1699C>G) c.*911C>G (n.*911C>G) c.1867C>G (p.Arg623Gly) | |
16 | g.89935277C>T | CA397475468 | TUBB3 | c.826C>T (p.Arg276Trp) n.4247C>T c.610C>T (p.Arg204Trp) c.277+1699C>T (n.277+1699C>T) c.*911C>T (n.*911C>T) c.1867C>T (p.Arg623Trp) | ClinVar gnomAD v4 |
16 | g.89935278G>A | CA8256169 | TUBB3 | c.827G>A (p.Arg276Gln) n.4248G>A c.611G>A (p.Arg204Gln) c.277+1700G>A (n.277+1700G>A) c.*912G>A (n.*912G>A) c.1868G>A (p.Arg623Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.89935278G>C | CA397475470 | TUBB3 | c.827G>C (p.Arg276Pro) n.4248G>C c.611G>C (p.Arg204Pro) c.277+1700G>C (n.277+1700G>C) c.*912G>C (n.*912G>C) c.1868G>C (p.Arg623Pro) | |
16 | g.89935278G= | CA2242020167 | TUBB3 | c.827G= (p.Arg276=) n.4248G= c.611G= (p.Arg204=) c.277+1700G= (n.277+1700G=) c.*912G= (n.*912G=) c.1868G= (p.Arg623=) | |
16 | g.89935278G>T | CA397475472 | TUBB3 | c.827G>T (p.Arg276Leu) n.4248G>T c.611G>T (p.Arg204Leu) c.277+1700G>T (n.277+1700G>T) c.*912G>T (n.*912G>T) c.1868G>T (p.Arg623Leu) | |
16 | g.89935279G>A | CA8256170 | TUBB3 | c.828G>A (p.Arg276=) n.4249G>A c.612G>A (p.Arg204=) c.277+1701G>A (n.277+1701G>A) c.*913G>A (n.*913G>A) c.1869G>A (p.Arg623=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.89935279G>C | CA497381336 | TUBB3 | c.828G>C (p.Arg276=) n.4249G>C c.612G>C (p.Arg204=) c.277+1701G>C (n.277+1701G>C) c.*913G>C (n.*913G>C) c.1869G>C (p.Arg623=) | |
16 | g.89935279G= | CA2242020170 | TUBB3 | c.828G= (p.Arg276=) n.4249G= c.612G= (p.Arg204=) c.277+1701G= (n.277+1701G=) c.*913G= (n.*913G=) c.1869G= (p.Arg623=) | |
16 | g.89935279G>T | CA497381335 | TUBB3 | c.828G>T (p.Arg276=) n.4249G>T c.612G>T (p.Arg204=) c.277+1701G>T (n.277+1701G>T) c.*913G>T (n.*913G>T) c.1869G>T (p.Arg623=) | |
16 | g.89935280G>A | CA397475477 | TUBB3 | c.829G>A (p.Gly277Ser) n.4250G>A c.613G>A (p.Gly205Ser) c.277+1702G>A (n.277+1702G>A) c.*914G>A (n.*914G>A) c.1870G>A (p.Gly624Ser) | COSMIC |
16 | g.89935280G>C | CA397475475 | TUBB3 | c.829G>C (p.Gly277Arg) n.4250G>C c.613G>C (p.Gly205Arg) c.277+1702G>C (n.277+1702G>C) c.*914G>C (n.*914G>C) c.1870G>C (p.Gly624Arg) | |
16 | g.89935280G>T | CA397475478 | TUBB3 | c.829G>T (p.Gly277Cys) n.4250G>T c.613G>T (p.Gly205Cys) c.277+1702G>T (n.277+1702G>T) c.*914G>T (n.*914G>T) c.1870G>T (p.Gly624Cys) | |
16 | g.89935281G>A | CA397475480 | TUBB3 | c.830G>A (p.Gly277Asp) n.4251G>A c.614G>A (p.Gly205Asp) c.277+1703G>A (n.277+1703G>A) c.*915G>A (n.*915G>A) c.1871G>A (p.Gly624Asp) | dbSNP |
16 | g.89935281G>C | CA397475481 | TUBB3 | c.830G>C (p.Gly277Ala) n.4251G>C c.614G>C (p.Gly205Ala) c.277+1703G>C (n.277+1703G>C) c.*915G>C (n.*915G>C) c.1871G>C (p.Gly624Ala) | |
16 | g.89935281G= | CA2242020172 | TUBB3 | c.830G= (p.Gly277=) n.4251G= c.614G= (p.Gly205=) c.277+1703G= (n.277+1703G=) c.*915G= (n.*915G=) c.1871G= (p.Gly624=) | |
16 | g.89935281G>T | CA397475482 | TUBB3 | c.830G>T (p.Gly277Val) n.4251G>T c.614G>T (p.Gly205Val) c.277+1703G>T (n.277+1703G>T) c.*915G>T (n.*915G>T) c.1871G>T (p.Gly624Val) | |
16 | g.89935282C>A | CA497381337 | TUBB3 | c.831C>A (p.Gly277=) n.4252C>A c.615C>A (p.Gly205=) c.277+1704C>A (n.277+1704C>A) c.*916C>A (n.*916C>A) c.1872C>A (p.Gly624=) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.89935282C= | CA2242020174 | TUBB3 | c.831C= (p.Gly277=) n.4252C= c.615C= (p.Gly205=) c.277+1704C= (n.277+1704C=) c.*916C= (n.*916C=) c.1872C= (p.Gly624=) | |
16 | g.89935282C>G | CA497381338 | TUBB3 | c.831C>G (p.Gly277=) n.4252C>G c.615C>G (p.Gly205=) c.277+1704C>G (n.277+1704C>G) c.*916C>G (n.*916C>G) c.1872C>G (p.Gly624=) | |
16 | g.89935282C>T | CA497381339 | TUBB3 | c.831C>T (p.Gly277=) n.4252C>T c.615C>T (p.Gly205=) c.277+1704C>T (n.277+1704C>T) c.*916C>T (n.*916C>T) c.1872C>T (p.Gly624=) | |
16 | g.89935283A>C | CA397475484 | TUBB3 | c.832A>C (p.Ser278Arg) n.4253A>C c.616A>C (p.Ser206Arg) c.277+1705A>C (n.277+1705A>C) c.*917A>C (n.*917A>C) c.1873A>C (p.Ser625Arg) | |
16 | g.89935283A>G | CA397475485 | TUBB3 | c.832A>G (p.Ser278Gly) n.4253A>G c.616A>G (p.Ser206Gly) c.277+1705A>G (n.277+1705A>G) c.*917A>G (n.*917A>G) c.1873A>G (p.Ser625Gly) | |
16 | g.89935283A>T | CA397475487 | TUBB3 | c.832A>T (p.Ser278Cys) n.4253A>T c.616A>T (p.Ser206Cys) c.277+1705A>T (n.277+1705A>T) c.*917A>T (n.*917A>T) c.1873A>T (p.Ser625Cys) | |
16 | g.89935284G>A | CA397475492 | TUBB3 | c.833G>A (p.Ser278Asn) n.4254G>A c.617G>A (p.Ser206Asn) c.277+1706G>A (n.277+1706G>A) c.*918G>A (n.*918G>A) c.1874G>A (p.Ser625Asn) | ClinVar gnomAD v4 |
16 | g.89935284G>C | CA397475489 | TUBB3 | c.833G>C (p.Ser278Thr) n.4254G>C c.617G>C (p.Ser206Thr) c.277+1706G>C (n.277+1706G>C) c.*918G>C (n.*918G>C) c.1874G>C (p.Ser625Thr) | |
16 | g.89935284G>T | CA397475491 | TUBB3 | c.833G>T (p.Ser278Ile) n.4254G>T c.617G>T (p.Ser206Ile) c.277+1706G>T (n.277+1706G>T) c.*918G>T (n.*918G>T) c.1874G>T (p.Ser625Ile) | |
16 | g.89935285C>A | CA397475494 | TUBB3 | c.834C>A (p.Ser278Arg) n.4255C>A c.618C>A (p.Ser206Arg) c.277+1707C>A (n.277+1707C>A) c.*919C>A (n.*919C>A) c.1875C>A (p.Ser625Arg) | |
16 | g.89935285C= | CA2242020178 | TUBB3 | c.834C= (p.Ser278=) n.4255C= c.618C= (p.Ser206=) c.277+1707C= (n.277+1707C=) c.*919C= (n.*919C=) c.1875C= (p.Ser625=) | |
16 | g.89935285C>G | CA397475495 | TUBB3 | c.834C>G (p.Ser278Arg) n.4255C>G c.618C>G (p.Ser206Arg) c.277+1707C>G (n.277+1707C>G) c.*919C>G (n.*919C>G) c.1875C>G (p.Ser625Arg) | ClinVar dbSNP |
16 | g.89935285C>T | CA497381346 | TUBB3 | c.834C>T (p.Ser278=) n.4255C>T c.618C>T (p.Ser206=) c.277+1707C>T (n.277+1707C>T) c.*919C>T (n.*919C>T) c.1875C>T (p.Ser625=) | gnomAD v4 |
16 | g.89935286C>A | CA397475496 | TUBB3 | c.835C>A (p.Gln279Lys) n.4256C>A c.619C>A (p.Gln207Lys) c.277+1708C>A (n.277+1708C>A) c.*920C>A (n.*920C>A) c.1876C>A (p.Gln626Lys) | |
16 | g.89935286C>G | CA397475497 | TUBB3 | c.835C>G (p.Gln279Glu) n.4256C>G c.619C>G (p.Gln207Glu) c.277+1708C>G (n.277+1708C>G) c.*920C>G (n.*920C>G) c.1876C>G (p.Gln626Glu) | |
16 | g.89935286C>T | CA397475498 | TUBB3 | c.835C>T (p.Gln279Ter) n.4256C>T c.619C>T (p.Gln207Ter) c.277+1708C>T (n.277+1708C>T) c.*920C>T (n.*920C>T) c.1876C>T (p.Gln626Ter) | |
16 | g.89935287A= | CA2242020183 | TUBB3 | c.836A= (p.Gln279=) n.4257A= c.620A= (p.Gln207=) c.277+1709A= (n.277+1709A=) c.*921A= (n.*921A=) c.1877A= (p.Gln626=) | |
16 | g.89935287A>C | CA397475502 | TUBB3 | c.836A>C (p.Gln279Pro) n.4257A>C c.620A>C (p.Gln207Pro) c.277+1709A>C (n.277+1709A>C) c.*921A>C (n.*921A>C) c.1877A>C (p.Gln626Pro) | |
16 | g.89935287A>G | CA397475499 | TUBB3 | c.836A>G (p.Gln279Arg) n.4257A>G c.620A>G (p.Gln207Arg) c.277+1709A>G (n.277+1709A>G) c.*921A>G (n.*921A>G) c.1877A>G (p.Gln626Arg) | ClinVar dbSNP |
16 | g.89935287A>T | CA397475501 | TUBB3 | c.836A>T (p.Gln279Leu) n.4257A>T c.620A>T (p.Gln207Leu) c.277+1709A>T (n.277+1709A>T) c.*921A>T (n.*921A>T) c.1877A>T (p.Gln626Leu) | |
16 | g.89935288G>A | CA497381348 | TUBB3 | c.837G>A (p.Gln279=) n.4258G>A c.621G>A (p.Gln207=) c.277+1710G>A (n.277+1710G>A) c.*922G>A (n.*922G>A) c.1878G>A (p.Gln626=) | |
16 | g.89935288G>C | CA397475504 | TUBB3 | c.837G>C (p.Gln279His) n.4258G>C c.621G>C (p.Gln207His) c.277+1710G>C (n.277+1710G>C) c.*922G>C (n.*922G>C) c.1878G>C (p.Gln626His) | |
16 | g.89935288G>T | CA397475505 | TUBB3 | c.837G>T (p.Gln279His) n.4258G>T c.621G>T (p.Gln207His) c.277+1710G>T (n.277+1710G>T) c.*922G>T (n.*922G>T) c.1878G>T (p.Gln626His) | |
16 | g.89935289C>A | CA397475507 | TUBB3 | c.838C>A (p.Gln280Lys) n.4259C>A c.622C>A (p.Gln208Lys) c.277+1711C>A (n.277+1711C>A) c.*923C>A (n.*923C>A) c.1879C>A (p.Gln627Lys) | |
16 | g.89935289C>G | CA397475508 | TUBB3 | c.838C>G (p.Gln280Glu) n.4259C>G c.622C>G (p.Gln208Glu) c.277+1711C>G (n.277+1711C>G) c.*923C>G (n.*923C>G) c.1879C>G (p.Gln627Glu) | |
16 | g.89935289C>T | CA397475510 | TUBB3 | c.838C>T (p.Gln280Ter) n.4259C>T c.622C>T (p.Gln208Ter) c.277+1711C>T (n.277+1711C>T) c.*923C>T (n.*923C>T) c.1879C>T (p.Gln627Ter) | |
16 | g.89935290A= | CA2242020186 | TUBB3 | c.839A= (p.Gln280=) n.4260A= c.623A= (p.Gln208=) c.277+1712A= (n.277+1712A=) c.*924A= (n.*924A=) c.1880A= (p.Gln627=) | |
16 | g.89935290A>C | CA397475512 | TUBB3 | c.839A>C (p.Gln280Pro) n.4260A>C c.623A>C (p.Gln208Pro) c.277+1712A>C (n.277+1712A>C) c.*924A>C (n.*924A>C) c.1880A>C (p.Gln627Pro) | |
16 | g.89935290A>G | CA397475513 | TUBB3 | c.839A>G (p.Gln280Arg) n.4260A>G c.623A>G (p.Gln208Arg) c.277+1712A>G (n.277+1712A>G) c.*924A>G (n.*924A>G) c.1880A>G (p.Gln627Arg) | |
16 | g.89935290A>T | CA8256171 | TUBB3 | c.839A>T (p.Gln280Leu) n.4260A>T c.623A>T (p.Gln208Leu) c.277+1712A>T (n.277+1712A>T) c.*924A>T (n.*924A>T) c.1880A>T (p.Gln627Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.89935291G>A | CA497381350 | TUBB3 | c.840G>A (p.Gln280=) n.4261G>A c.624G>A (p.Gln208=) c.277+1713G>A (n.277+1713G>A) c.*925G>A (n.*925G>A) c.1881G>A (p.Gln627=) | gnomAD v4 |
16 | g.89935291G>C | CA397475516 | TUBB3 | c.840G>C (p.Gln280His) n.4261G>C c.624G>C (p.Gln208His) c.277+1713G>C (n.277+1713G>C) c.*925G>C (n.*925G>C) c.1881G>C (p.Gln627His) | |
16 | g.89935291G>T | CA397475520 | TUBB3 | c.840G>T (p.Gln280His) n.4261G>T c.624G>T (p.Gln208His) c.277+1713G>T (n.277+1713G>T) c.*925G>T (n.*925G>T) c.1881G>T (p.Gln627His) | |
16 | g.89935292T>A | CA397475521 | TUBB3 | c.841T>A (p.Tyr281Asn) n.4262T>A c.625T>A (p.Tyr209Asn) c.277+1714T>A (n.277+1714T>A) c.*926T>A (n.*926T>A) c.1882T>A (p.Tyr628Asn) | |
16 | g.89935292T>C | CA397475523 | TUBB3 | c.841T>C (p.Tyr281His) n.4262T>C c.625T>C (p.Tyr209His) c.277+1714T>C (n.277+1714T>C) c.*926T>C (n.*926T>C) c.1882T>C (p.Tyr628His) | |
16 | g.89935292T>G | CA397475525 | TUBB3 | c.841T>G (p.Tyr281Asp) n.4262T>G c.625T>G (p.Tyr209Asp) c.277+1714T>G (n.277+1714T>G) c.*926T>G (n.*926T>G) c.1882T>G (p.Tyr628Asp) | |
16 | g.89935293A>C | CA397475530 | TUBB3 | c.842A>C (p.Tyr281Ser) n.4263A>C c.626A>C (p.Tyr209Ser) c.277+1715A>C (n.277+1715A>C) c.*927A>C (n.*927A>C) c.1883A>C (p.Tyr628Ser) | |
16 | g.89935293A>G | CA397475526 | TUBB3 | c.842A>G (p.Tyr281Cys) n.4263A>G c.626A>G (p.Tyr209Cys) c.277+1715A>G (n.277+1715A>G) c.*927A>G (n.*927A>G) c.1883A>G (p.Tyr628Cys) | |
16 | g.89935293A>T | CA397475528 | TUBB3 | c.842A>T (p.Tyr281Phe) n.4263A>T c.626A>T (p.Tyr209Phe) c.277+1715A>T (n.277+1715A>T) c.*927A>T (n.*927A>T) c.1883A>T (p.Tyr628Phe) | |
16 | g.89935294C>A | CA397475531 | TUBB3 | c.843C>A (p.Tyr281Ter) n.4264C>A c.627C>A (p.Tyr209Ter) c.277+1716C>A (n.277+1716C>A) c.*928C>A (n.*928C>A) c.1884C>A (p.Tyr628Ter) | |
16 | g.89935294C>G | CA397475533 | TUBB3 | c.843C>G (p.Tyr281Ter) n.4264C>G c.627C>G (p.Tyr209Ter) c.277+1716C>G (n.277+1716C>G) c.*928C>G (n.*928C>G) c.1884C>G (p.Tyr628Ter) | |
16 | g.89935294C>T | CA497381354 | TUBB3 | c.843C>T (p.Tyr281=) n.4264C>T c.627C>T (p.Tyr209=) c.277+1716C>T (n.277+1716C>T) c.*928C>T (n.*928C>T) c.1884C>T (p.Tyr628=) | |
16 | g.89935295C>A | CA497381355 | TUBB3 | c.844C>A (p.Arg282=) n.4265C>A c.628C>A (p.Arg210=) c.277+1717C>A (n.277+1717C>A) c.*929C>A (n.*929C>A) c.1885C>A (p.Arg629=) | gnomAD v4 |
16 | g.89935295C= | CA2242020189 | TUBB3 | c.844C= (p.Arg282=) n.4265C= c.628C= (p.Arg210=) c.277+1717C= (n.277+1717C=) c.*929C= (n.*929C=) c.1885C= (p.Arg629=) | |
16 | g.89935295C>G | CA397475536 | TUBB3 | c.844C>G (p.Arg282Gly) n.4265C>G c.628C>G (p.Arg210Gly) c.277+1717C>G (n.277+1717C>G) c.*929C>G (n.*929C>G) c.1885C>G (p.Arg629Gly) | ClinVar |
16 | g.89935295C>T | CA397475538 | TUBB3 | c.844C>T (p.Arg282Trp) n.4265C>T c.628C>T (p.Arg210Trp) c.277+1717C>T (n.277+1717C>T) c.*929C>T (n.*929C>T) c.1885C>T (p.Arg629Trp) | dbSNP gnomAD v4 |
16 | g.89935296G>A | CA397475540 | TUBB3 | c.845G>A (p.Arg282Gln) n.4266G>A c.629G>A (p.Arg210Gln) c.277+1718G>A (n.277+1718G>A) c.*930G>A (n.*930G>A) c.1886G>A (p.Arg629Gln) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
16 | g.89935296G>C | CA16620315 | TUBB3 | c.845G>C (p.Arg282Pro) n.4266G>C c.629G>C (p.Arg210Pro) c.277+1718G>C (n.277+1718G>C) c.*930G>C (n.*930G>C) c.1886G>C (p.Arg629Pro) | ClinVar dbSNP |
16 | g.89935296G= | CA2242020196 | TUBB3 | c.845G= (p.Arg282=) n.4266G= c.629G= (p.Arg210=) c.277+1718G= (n.277+1718G=) c.*930G= (n.*930G=) c.1886G= (p.Arg629=) | |
16 | g.89935296G>T | CA397475544 | TUBB3 | c.845G>T (p.Arg282Leu) n.4266G>T c.629G>T (p.Arg210Leu) c.277+1718G>T (n.277+1718G>T) c.*930G>T (n.*930G>T) c.1886G>T (p.Arg629Leu) |