UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.89935145A>C | CA397475133 | TUBB3 | c.694A>C (p.Thr232Pro) n.4115A>C c.478A>C (p.Thr160Pro) c.277+1567A>C (n.277+1567A>C) c.*779A>C (n.*779A>C) c.1735A>C (p.Thr579Pro) | |
| 16 | g.89935145A>G | CA397475134 | TUBB3 | c.694A>G (p.Thr232Ala) n.4115A>G c.478A>G (p.Thr160Ala) c.277+1567A>G (n.277+1567A>G) c.*779A>G (n.*779A>G) c.1735A>G (p.Thr579Ala) | |
| 16 | g.89935145A>T | CA397475135 | TUBB3 | c.694A>T (p.Thr232Ser) n.4115A>T c.478A>T (p.Thr160Ser) c.277+1567A>T (n.277+1567A>T) c.*779A>T (n.*779A>T) c.1735A>T (p.Thr579Ser) | |
| 16 | g.89935146C>A | CA397475138 | TUBB3 | c.695C>A (p.Thr232Asn) n.4116C>A c.479C>A (p.Thr160Asn) c.277+1568C>A (n.277+1568C>A) c.*780C>A (n.*780C>A) c.1736C>A (p.Thr579Asn) | |
| 16 | g.89935146C>G | CA397475137 | TUBB3 | c.695C>G (p.Thr232Ser) n.4116C>G c.479C>G (p.Thr160Ser) c.277+1568C>G (n.277+1568C>G) c.*780C>G (n.*780C>G) c.1736C>G (p.Thr579Ser) | |
| 16 | g.89935146C>T | CA397475136 | TUBB3 | c.695C>T (p.Thr232Ile) n.4116C>T c.479C>T (p.Thr160Ile) c.277+1568C>T (n.277+1568C>T) c.*780C>T (n.*780C>T) c.1736C>T (p.Thr579Ile) | |
| 16 | g.89935147C>A | CA497381098 | TUBB3 | c.696C>A (p.Thr232=) n.4117C>A c.480C>A (p.Thr160=) c.277+1569C>A (n.277+1569C>A) c.*781C>A (n.*781C>A) c.1737C>A (p.Thr579=) | |
| 16 | g.89935147C>G | CA497381099 | TUBB3 | c.696C>G (p.Thr232=) n.4117C>G c.480C>G (p.Thr160=) c.277+1569C>G (n.277+1569C>G) c.*781C>G (n.*781C>G) c.1737C>G (p.Thr579=) | gnomAD v4 |
| 16 | g.89935147C>T | CA497381100 | TUBB3 | c.696C>T (p.Thr232=) n.4117C>T c.480C>T (p.Thr160=) c.277+1569C>T (n.277+1569C>T) c.*781C>T (n.*781C>T) c.1737C>T (p.Thr579=) | COSMIC |
| 16 | g.89935148A>C | CA397475139 | TUBB3 | c.697A>C (p.Met233Leu) n.4118A>C c.481A>C (p.Met161Leu) c.277+1570A>C (n.277+1570A>C) c.*782A>C (n.*782A>C) c.1738A>C (p.Met580Leu) | |
| 16 | g.89935148A>G | CA397475140 | TUBB3 | c.697A>G (p.Met233Val) n.4118A>G c.481A>G (p.Met161Val) c.277+1570A>G (n.277+1570A>G) c.*782A>G (n.*782A>G) c.1738A>G (p.Met580Val) | |
| 16 | g.89935148A>T | CA397475141 | TUBB3 | c.697A>T (p.Met233Leu) n.4118A>T c.481A>T (p.Met161Leu) c.277+1570A>T (n.277+1570A>T) c.*782A>T (n.*782A>T) c.1738A>T (p.Met580Leu) | |
| 16 | g.89935149T>A | CA397475142 | TUBB3 | c.698T>A (p.Met233Lys) n.4119T>A c.482T>A (p.Met161Lys) c.277+1571T>A (n.277+1571T>A) c.*783T>A (n.*783T>A) c.1739T>A (p.Met580Lys) | gnomAD v4 |
| 16 | g.89935149T>C | CA397475143 | TUBB3 | c.698T>C (p.Met233Thr) n.4119T>C c.482T>C (p.Met161Thr) c.277+1571T>C (n.277+1571T>C) c.*783T>C (n.*783T>C) c.1739T>C (p.Met580Thr) | |
| 16 | g.89935149T>G | CA397475144 | TUBB3 | c.698T>G (p.Met233Arg) n.4119T>G c.482T>G (p.Met161Arg) c.277+1571T>G (n.277+1571T>G) c.*783T>G (n.*783T>G) c.1739T>G (p.Met580Arg) | gnomAD v4 |
| 16 | g.89935150G>A | CA397475145 | TUBB3 | c.699G>A (p.Met233Ile) n.4120G>A c.483G>A (p.Met161Ile) c.277+1572G>A (n.277+1572G>A) c.*784G>A (n.*784G>A) c.1740G>A (p.Met580Ile) | |
| 16 | g.89935150G>C | CA397475146 | TUBB3 | c.699G>C (p.Met233Ile) n.4120G>C c.483G>C (p.Met161Ile) c.277+1572G>C (n.277+1572G>C) c.*784G>C (n.*784G>C) c.1740G>C (p.Met580Ile) | |
| 16 | g.89935150G>T | CA397475147 | TUBB3 | c.699G>T (p.Met233Ile) n.4120G>T c.483G>T (p.Met161Ile) c.277+1572G>T (n.277+1572G>T) c.*784G>T (n.*784G>T) c.1740G>T (p.Met580Ile) | |
| 16 | g.89935151A>C | CA397475148 | TUBB3 | c.700A>C (p.Ser234Arg) n.4121A>C c.484A>C (p.Ser162Arg) c.277+1573A>C (n.277+1573A>C) c.*785A>C (n.*785A>C) c.1741A>C (p.Ser581Arg) | |
| 16 | g.89935151A>G | CA397475149 | TUBB3 | c.700A>G (p.Ser234Gly) n.4121A>G c.484A>G (p.Ser162Gly) c.277+1573A>G (n.277+1573A>G) c.*785A>G (n.*785A>G) c.1741A>G (p.Ser581Gly) | |
| 16 | g.89935151A>T | CA397475150 | TUBB3 | c.700A>T (p.Ser234Cys) n.4121A>T c.484A>T (p.Ser162Cys) c.277+1573A>T (n.277+1573A>T) c.*785A>T (n.*785A>T) c.1741A>T (p.Ser581Cys) | |
| 16 | g.89935152G>A | CA397475153 | TUBB3 | c.701G>A (p.Ser234Asn) n.4122G>A c.485G>A (p.Ser162Asn) c.277+1574G>A (n.277+1574G>A) c.*786G>A (n.*786G>A) c.1742G>A (p.Ser581Asn) | |
| 16 | g.89935152G>C | CA397475152 | TUBB3 | c.701G>C (p.Ser234Thr) n.4122G>C c.485G>C (p.Ser162Thr) c.277+1574G>C (n.277+1574G>C) c.*786G>C (n.*786G>C) c.1742G>C (p.Ser581Thr) | |
| 16 | g.89935152G>T | CA397475151 | TUBB3 | c.701G>T (p.Ser234Ile) n.4122G>T c.485G>T (p.Ser162Ile) c.277+1574G>T (n.277+1574G>T) c.*786G>T (n.*786G>T) c.1742G>T (p.Ser581Ile) | |
| 16 | g.89935153C>A | CA397475154 | TUBB3 | c.702C>A (p.Ser234Arg) n.4123C>A c.486C>A (p.Ser162Arg) c.277+1575C>A (n.277+1575C>A) c.*787C>A (n.*787C>A) c.1743C>A (p.Ser581Arg) | |
| 16 | g.89935153C= | CA2242019981 | TUBB3 | c.702C= (p.Ser234=) n.4123C= c.486C= (p.Ser162=) c.277+1575C= (n.277+1575C=) c.*787C= (n.*787C=) c.1743C= (p.Ser581=) | |
| 16 | g.89935153C>G | CA397475155 | TUBB3 | c.702C>G (p.Ser234Arg) n.4123C>G c.486C>G (p.Ser162Arg) c.277+1575C>G (n.277+1575C>G) c.*787C>G (n.*787C>G) c.1743C>G (p.Ser581Arg) | |
| 16 | g.89935153C>T | CA173799 | TUBB3 | c.702C>T (p.Ser234=) n.4123C>T c.486C>T (p.Ser162=) c.277+1575C>T (n.277+1575C>T) c.*787C>T (n.*787C>T) c.1743C>T (p.Ser581=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89935154G>A | CA397475156 | TUBB3 | c.703G>A (p.Gly235Arg) n.4124G>A c.487G>A (p.Gly163Arg) c.277+1576G>A (n.277+1576G>A) c.*788G>A (n.*788G>A) c.1744G>A (p.Gly582Arg) | dbSNP gnomAD v4 COSMIC |
| 16 | g.89935154G>C | CA397475157 | TUBB3 | c.703G>C (p.Gly235Arg) n.4124G>C c.487G>C (p.Gly163Arg) c.277+1576G>C (n.277+1576G>C) c.*788G>C (n.*788G>C) c.1744G>C (p.Gly582Arg) | |
| 16 | g.89935154G= | CA2242019983 | TUBB3 | c.703G= (p.Gly235=) n.4124G= c.487G= (p.Gly163=) c.277+1576G= (n.277+1576G=) c.*788G= (n.*788G=) c.1744G= (p.Gly582=) | |
| 16 | g.89935154G>T | CA397475158 | TUBB3 | c.703G>T (p.Gly235Ter) n.4124G>T c.487G>T (p.Gly163Ter) c.277+1576G>T (n.277+1576G>T) c.*788G>T (n.*788G>T) c.1744G>T (p.Gly582Ter) | |
| 16 | g.89935155G>A | CA397475159 | TUBB3 | c.704G>A (p.Gly235Glu) n.4125G>A c.488G>A (p.Gly163Glu) c.277+1577G>A (n.277+1577G>A) c.*789G>A (n.*789G>A) c.1745G>A (p.Gly582Glu) | gnomAD v4 COSMIC |
| 16 | g.89935155G>C | CA397475160 | TUBB3 | c.704G>C (p.Gly235Ala) n.4125G>C c.488G>C (p.Gly163Ala) c.277+1577G>C (n.277+1577G>C) c.*789G>C (n.*789G>C) c.1745G>C (p.Gly582Ala) | |
| 16 | g.89935155G>T | CA397475161 | TUBB3 | c.704G>T (p.Gly235Val) n.4125G>T c.488G>T (p.Gly163Val) c.277+1577G>T (n.277+1577G>T) c.*789G>T (n.*789G>T) c.1745G>T (p.Gly582Val) | |
| 16 | g.89935156A>C | CA497381113 | TUBB3 | c.705A>C (p.Gly235=) n.4126A>C c.489A>C (p.Gly163=) c.277+1578A>C (n.277+1578A>C) c.*790A>C (n.*790A>C) c.1746A>C (p.Gly582=) | |
| 16 | g.89935156A>G | CA497381114 | TUBB3 | c.705A>G (p.Gly235=) n.4126A>G c.489A>G (p.Gly163=) c.277+1578A>G (n.277+1578A>G) c.*790A>G (n.*790A>G) c.1746A>G (p.Gly582=) | |
| 16 | g.89935156A>T | CA497381115 | TUBB3 | c.705A>T (p.Gly235=) n.4126A>T c.489A>T (p.Gly163=) c.277+1578A>T (n.277+1578A>T) c.*790A>T (n.*790A>T) c.1746A>T (p.Gly582=) | |
| 16 | g.89935157G>A | CA397475162 | TUBB3 | c.706G>A (p.Val236Ile) n.4127G>A c.490G>A (p.Val164Ile) c.277+1579G>A (n.277+1579G>A) c.*791G>A (n.*791G>A) c.1747G>A (p.Val583Ile) | COSMIC |
| 16 | g.89935157G>C | CA397475163 | TUBB3 | c.706G>C (p.Val236Leu) n.4127G>C c.490G>C (p.Val164Leu) c.277+1579G>C (n.277+1579G>C) c.*791G>C (n.*791G>C) c.1747G>C (p.Val583Leu) | |
| 16 | g.89935157G>T | CA397475164 | TUBB3 | c.706G>T (p.Val236Phe) n.4127G>T c.490G>T (p.Val164Phe) c.277+1579G>T (n.277+1579G>T) c.*791G>T (n.*791G>T) c.1747G>T (p.Val583Phe) | |
| 16 | g.89935158T>A | CA397475166 | TUBB3 | c.707T>A (p.Val236Asp) n.4128T>A c.491T>A (p.Val164Asp) c.277+1580T>A (n.277+1580T>A) c.*792T>A (n.*792T>A) c.1748T>A (p.Val583Asp) | |
| 16 | g.89935158T>C | CA397475167 | TUBB3 | c.707T>C (p.Val236Ala) n.4128T>C c.491T>C (p.Val164Ala) c.277+1580T>C (n.277+1580T>C) c.*792T>C (n.*792T>C) c.1748T>C (p.Val583Ala) | |
| 16 | g.89935158T>G | CA397475165 | TUBB3 | c.707T>G (p.Val236Gly) n.4128T>G c.491T>G (p.Val164Gly) c.277+1580T>G (n.277+1580T>G) c.*792T>G (n.*792T>G) c.1748T>G (p.Val583Gly) | |
| 16 | g.89935159C>A | CA497381118 | TUBB3 | c.708C>A (p.Val236=) n.4129C>A c.492C>A (p.Val164=) c.277+1581C>A (n.277+1581C>A) c.*793C>A (n.*793C>A) c.1749C>A (p.Val583=) | |
| 16 | g.89935159C= | CA2242019986 | TUBB3 | c.708C= (p.Val236=) n.4129C= c.492C= (p.Val164=) c.277+1581C= (n.277+1581C=) c.*793C= (n.*793C=) c.1749C= (p.Val583=) | |
| 16 | g.89935159C>G | CA497381120 | TUBB3 | c.708C>G (p.Val236=) n.4129C>G c.492C>G (p.Val164=) c.277+1581C>G (n.277+1581C>G) c.*793C>G (n.*793C>G) c.1749C>G (p.Val583=) | |
| 16 | g.89935159C>T | CA8256154 | TUBB3 | c.708C>T (p.Val236=) n.4129C>T c.492C>T (p.Val164=) c.277+1581C>T (n.277+1581C>T) c.*793C>T (n.*793C>T) c.1749C>T (p.Val583=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.89935160A>C | CA397475168 | TUBB3 | c.709A>C (p.Thr237Pro) n.4130A>C c.493A>C (p.Thr165Pro) c.277+1582A>C (n.277+1582A>C) c.*794A>C (n.*794A>C) c.1750A>C (p.Thr584Pro) | |
| 16 | g.89935160A>G | CA397475169 | TUBB3 | c.709A>G (p.Thr237Ala) n.4130A>G c.493A>G (p.Thr165Ala) c.277+1582A>G (n.277+1582A>G) c.*794A>G (n.*794A>G) c.1750A>G (p.Thr584Ala) | |
| 16 | g.89935160A>T | CA397475170 | TUBB3 | c.709A>T (p.Thr237Ser) n.4130A>T c.493A>T (p.Thr165Ser) c.277+1582A>T (n.277+1582A>T) c.*794A>T (n.*794A>T) c.1750A>T (p.Thr584Ser) | |
| 16 | g.89935161C>A | CA397475173 | TUBB3 | c.710C>A (p.Thr237Asn) n.4131C>A c.494C>A (p.Thr165Asn) c.277+1583C>A (n.277+1583C>A) c.*795C>A (n.*795C>A) c.1751C>A (p.Thr584Asn) | |
| 16 | g.89935161C>G | CA397475172 | TUBB3 | c.710C>G (p.Thr237Ser) n.4131C>G c.494C>G (p.Thr165Ser) c.277+1583C>G (n.277+1583C>G) c.*795C>G (n.*795C>G) c.1751C>G (p.Thr584Ser) | |
| 16 | g.89935161C>T | CA397475171 | TUBB3 | c.710C>T (p.Thr237Ile) n.4131C>T c.494C>T (p.Thr165Ile) c.277+1583C>T (n.277+1583C>T) c.*795C>T (n.*795C>T) c.1751C>T (p.Thr584Ile) | |
| 16 | g.89935162C>A | CA497381126 | TUBB3 | c.711C>A (p.Thr237=) n.4132C>A c.495C>A (p.Thr165=) c.277+1584C>A (n.277+1584C>A) c.*796C>A (n.*796C>A) c.1752C>A (p.Thr584=) | |
| 16 | g.89935162C= | CA2242019989 | TUBB3 | c.711C= (p.Thr237=) n.4132C= c.495C= (p.Thr165=) c.277+1584C= (n.277+1584C=) c.*796C= (n.*796C=) c.1752C= (p.Thr584=) | |
| 16 | g.89935162C>G | CA497381123 | TUBB3 | c.711C>G (p.Thr237=) n.4132C>G c.495C>G (p.Thr165=) c.277+1584C>G (n.277+1584C>G) c.*796C>G (n.*796C>G) c.1752C>G (p.Thr584=) | |
| 16 | g.89935162C>T | CA497381121 | TUBB3 | c.711C>T (p.Thr237=) n.4132C>T c.495C>T (p.Thr165=) c.277+1584C>T (n.277+1584C>T) c.*796C>T (n.*796C>T) c.1752C>T (p.Thr584=) | dbSNP gnomAD v4 |
| 16 | g.89935163A= | CA2242019992 | TUBB3 | c.712A= (p.Thr238=) n.4133A= c.496A= (p.Thr166=) c.277+1585A= (n.277+1585A=) c.*797A= (n.*797A=) c.1753A= (p.Thr585=) | |
| 16 | g.89935163A>C | CA397475174 | TUBB3 | c.712A>C (p.Thr238Pro) n.4133A>C c.496A>C (p.Thr166Pro) c.277+1585A>C (n.277+1585A>C) c.*797A>C (n.*797A>C) c.1753A>C (p.Thr585Pro) | dbSNP |
| 16 | g.89935163A>G | CA397475175 | TUBB3 | c.712A>G (p.Thr238Ala) n.4133A>G c.496A>G (p.Thr166Ala) c.277+1585A>G (n.277+1585A>G) c.*797A>G (n.*797A>G) c.1753A>G (p.Thr585Ala) | |
| 16 | g.89935163A>T | CA397475176 | TUBB3 | c.712A>T (p.Thr238Ser) n.4133A>T c.496A>T (p.Thr166Ser) c.277+1585A>T (n.277+1585A>T) c.*797A>T (n.*797A>T) c.1753A>T (p.Thr585Ser) | |
| 16 | g.89935164C>A | CA397475177 | TUBB3 | c.713C>A (p.Thr238Asn) n.4134C>A c.497C>A (p.Thr166Asn) c.277+1586C>A (n.277+1586C>A) c.*798C>A (n.*798C>A) c.1754C>A (p.Thr585Asn) | |
| 16 | g.89935164C>G | CA397475178 | TUBB3 | c.713C>G (p.Thr238Ser) n.4134C>G c.497C>G (p.Thr166Ser) c.277+1586C>G (n.277+1586C>G) c.*798C>G (n.*798C>G) c.1754C>G (p.Thr585Ser) | |
| 16 | g.89935164C>T | CA397475179 | TUBB3 | c.713C>T (p.Thr238Ile) n.4134C>T c.497C>T (p.Thr166Ile) c.277+1586C>T (n.277+1586C>T) c.*798C>T (n.*798C>T) c.1754C>T (p.Thr585Ile) | |
| 16 | g.89935165C>A | CA497381129 | TUBB3 | c.714C>A (p.Thr238=) n.4135C>A c.498C>A (p.Thr166=) c.277+1587C>A (n.277+1587C>A) c.*799C>A (n.*799C>A) c.1755C>A (p.Thr585=) | |
| 16 | g.89935165C= | CA2242019994 | TUBB3 | c.714C= (p.Thr238=) n.4135C= c.498C= (p.Thr166=) c.277+1587C= (n.277+1587C=) c.*799C= (n.*799C=) c.1755C= (p.Thr585=) | |
| 16 | g.89935165C>G | CA497381131 | TUBB3 | c.714C>G (p.Thr238=) n.4135C>G c.498C>G (p.Thr166=) c.277+1587C>G (n.277+1587C>G) c.*799C>G (n.*799C>G) c.1755C>G (p.Thr585=) | |
| 16 | g.89935165C>T | CA497381133 | TUBB3 | c.714C>T (p.Thr238=) n.4135C>T c.498C>T (p.Thr166=) c.277+1587C>T (n.277+1587C>T) c.*799C>T (n.*799C>T) c.1755C>T (p.Thr585=) | dbSNP |
| 16 | g.89935166T>A | CA397475182 | TUBB3 | c.715T>A (p.Ser239Thr) n.4136T>A c.499T>A (p.Ser167Thr) c.277+1588T>A (n.277+1588T>A) c.*800T>A (n.*800T>A) c.1756T>A (p.Ser586Thr) | |
| 16 | g.89935166T>C | CA397475181 | TUBB3 | c.715T>C (p.Ser239Pro) n.4136T>C c.499T>C (p.Ser167Pro) c.277+1588T>C (n.277+1588T>C) c.*800T>C (n.*800T>C) c.1756T>C (p.Ser586Pro) | |
| 16 | g.89935166T>G | CA397475180 | TUBB3 | c.715T>G (p.Ser239Ala) n.4136T>G c.499T>G (p.Ser167Ala) c.277+1588T>G (n.277+1588T>G) c.*800T>G (n.*800T>G) c.1756T>G (p.Ser586Ala) | |
| 16 | g.89935167C>A | CA397475183 | TUBB3 | c.716C>A (p.Ser239Tyr) n.4137C>A c.500C>A (p.Ser167Tyr) c.277+1589C>A (n.277+1589C>A) c.*801C>A (n.*801C>A) c.1757C>A (p.Ser586Tyr) | |
| 16 | g.89935167C= | CA2242020000 | TUBB3 | c.716C= (p.Ser239=) n.4137C= c.500C= (p.Ser167=) c.277+1589C= (n.277+1589C=) c.*801C= (n.*801C=) c.1757C= (p.Ser586=) | |
| 16 | g.89935167C>G | CA397475185 | TUBB3 | c.716C>G (p.Ser239Cys) n.4137C>G c.500C>G (p.Ser167Cys) c.277+1589C>G (n.277+1589C>G) c.*801C>G (n.*801C>G) c.1757C>G (p.Ser586Cys) | COSMIC |
| 16 | g.89935167C>T | CA397475184 | TUBB3 | c.716C>T (p.Ser239Phe) n.4137C>T c.500C>T (p.Ser167Phe) c.277+1589C>T (n.277+1589C>T) c.*801C>T (n.*801C>T) c.1757C>T (p.Ser586Phe) | ClinVar dbSNP |
| 16 | g.89935168C>A | CA497381135 | TUBB3 | c.717C>A (p.Ser239=) n.4138C>A c.501C>A (p.Ser167=) c.277+1590C>A (n.277+1590C>A) c.*802C>A (n.*802C>A) c.1758C>A (p.Ser586=) | |
| 16 | g.89935168C>G | CA497381136 | TUBB3 | c.717C>G (p.Ser239=) n.4138C>G c.501C>G (p.Ser167=) c.277+1590C>G (n.277+1590C>G) c.*802C>G (n.*802C>G) c.1758C>G (p.Ser586=) | ClinVar dbSNP |
| 16 | g.89935168C>T | CA497381137 | TUBB3 | c.717C>T (p.Ser239=) n.4138C>T c.501C>T (p.Ser167=) c.277+1590C>T (n.277+1590C>T) c.*802C>T (n.*802C>T) c.1758C>T (p.Ser586=) | |
| 16 | g.89935169T>A | CA397475186 | TUBB3 | c.718T>A (p.Leu240Met) n.4139T>A c.502T>A (p.Leu168Met) c.277+1591T>A (n.277+1591T>A) c.*803T>A (n.*803T>A) c.1759T>A (p.Leu587Met) | |
| 16 | g.89935169T>C | CA497381143 | TUBB3 | c.718T>C (p.Leu240=) n.4139T>C c.502T>C (p.Leu168=) c.277+1591T>C (n.277+1591T>C) c.*803T>C (n.*803T>C) c.1759T>C (p.Leu587=) | |
| 16 | g.89935169T>G | CA397475187 | TUBB3 | c.718T>G (p.Leu240Val) n.4139T>G c.502T>G (p.Leu168Val) c.277+1591T>G (n.277+1591T>G) c.*803T>G (n.*803T>G) c.1759T>G (p.Leu587Val) | |
| 16 | g.89935170T>A | CA397475188 | TUBB3 | c.719T>A (p.Leu240Ter) n.4140T>A c.503T>A (p.Leu168Ter) c.277+1592T>A (n.277+1592T>A) c.*804T>A (n.*804T>A) c.1760T>A (p.Leu587Ter) | |
| 16 | g.89935170T>C | CA397475190 | TUBB3 | c.719T>C (p.Leu240Ser) n.4140T>C c.503T>C (p.Leu168Ser) c.277+1592T>C (n.277+1592T>C) c.*804T>C (n.*804T>C) c.1760T>C (p.Leu587Ser) | |
| 16 | g.89935170T>G | CA397475189 | TUBB3 | c.719T>G (p.Leu240Trp) n.4140T>G c.503T>G (p.Leu168Trp) c.277+1592T>G (n.277+1592T>G) c.*804T>G (n.*804T>G) c.1760T>G (p.Leu587Trp) | |
| 16 | g.89935171G>A | CA497381146 | TUBB3 | c.720G>A (p.Leu240=) n.4141G>A c.504G>A (p.Leu168=) c.277+1593G>A (n.277+1593G>A) c.*805G>A (n.*805G>A) c.1761G>A (p.Leu587=) | |
| 16 | g.89935171G>C | CA397475191 | TUBB3 | c.720G>C (p.Leu240Phe) n.4141G>C c.504G>C (p.Leu168Phe) c.277+1593G>C (n.277+1593G>C) c.*805G>C (n.*805G>C) c.1761G>C (p.Leu587Phe) | |
| 16 | g.89935171G>T | CA397475192 | TUBB3 | c.720G>T (p.Leu240Phe) n.4141G>T c.504G>T (p.Leu168Phe) c.277+1593G>T (n.277+1593G>T) c.*805G>T (n.*805G>T) c.1761G>T (p.Leu587Phe) | |
| 16 | g.89935172C>A | CA397475193 | TUBB3 | c.721C>A (p.Arg241Ser) n.4142C>A c.505C>A (p.Arg169Ser) c.277+1594C>A (n.277+1594C>A) c.*806C>A (n.*806C>A) c.1762C>A (p.Arg588Ser) | |
| 16 | g.89935172C= | CA2242020003 | TUBB3 | c.721C= (p.Arg241=) n.4142C= c.505C= (p.Arg169=) c.277+1594C= (n.277+1594C=) c.*806C= (n.*806C=) c.1762C= (p.Arg588=) | |
| 16 | g.89935172C>G | CA397475194 | TUBB3 | c.721C>G (p.Arg241Gly) n.4142C>G c.505C>G (p.Arg169Gly) c.277+1594C>G (n.277+1594C>G) c.*806C>G (n.*806C>G) c.1762C>G (p.Arg588Gly) | |
| 16 | g.89935172C>T | CA8256155 | TUBB3 | c.721C>T (p.Arg241Cys) n.4142C>T c.505C>T (p.Arg169Cys) c.277+1594C>T (n.277+1594C>T) c.*806C>T (n.*806C>T) c.1762C>T (p.Arg588Cys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 16 | g.89935173G>A | CA8256156 | TUBB3 | c.722G>A (p.Arg241His) n.4143G>A c.506G>A (p.Arg169His) c.277+1595G>A (n.277+1595G>A) c.*807G>A (n.*807G>A) c.1763G>A (p.Arg588His) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.89935173G>C | CA397475196 | TUBB3 | c.722G>C (p.Arg241Pro) n.4143G>C c.506G>C (p.Arg169Pro) c.277+1595G>C (n.277+1595G>C) c.*807G>C (n.*807G>C) c.1763G>C (p.Arg588Pro) | |
| 16 | g.89935173G= | CA2242020007 | TUBB3 | c.722G= (p.Arg241=) n.4143G= c.506G= (p.Arg169=) c.277+1595G= (n.277+1595G=) c.*807G= (n.*807G=) c.1763G= (p.Arg588=) | |
| 16 | g.89935173G>T | CA397475195 | TUBB3 | c.722G>T (p.Arg241Leu) n.4143G>T c.506G>T (p.Arg169Leu) c.277+1595G>T (n.277+1595G>T) c.*807G>T (n.*807G>T) c.1763G>T (p.Arg588Leu) | |
| 16 | g.89935174C>A | CA497381150 | TUBB3 | c.723C>A (p.Arg241=) n.4144C>A c.507C>A (p.Arg169=) c.277+1596C>A (n.277+1596C>A) c.*808C>A (n.*808C>A) c.1764C>A (p.Arg588=) | COSMIC |
| 16 | g.89935174C= | CA2242020010 | TUBB3 | c.723C= (p.Arg241=) n.4144C= c.507C= (p.Arg169=) c.277+1596C= (n.277+1596C=) c.*808C= (n.*808C=) c.1764C= (p.Arg588=) | |
| 16 | g.89935174C>G | CA497381151 | TUBB3 | c.723C>G (p.Arg241=) n.4144C>G c.507C>G (p.Arg169=) c.277+1596C>G (n.277+1596C>G) c.*808C>G (n.*808C>G) c.1764C>G (p.Arg588=) | dbSNP |
| 16 | g.89935174C>T | CA8256157 | TUBB3 | c.723C>T (p.Arg241=) n.4144C>T c.507C>T (p.Arg169=) c.277+1596C>T (n.277+1596C>T) c.*808C>T (n.*808C>T) c.1764C>T (p.Arg588=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89935175T>A | CA397475199 | TUBB3 | c.724T>A (p.Phe242Ile) n.4145T>A c.508T>A (p.Phe170Ile) c.277+1597T>A (n.277+1597T>A) c.*809T>A (n.*809T>A) c.1765T>A (p.Phe589Ile) | |
| 16 | g.89935175T>C | CA397475197 | TUBB3 | c.724T>C (p.Phe242Leu) n.4145T>C c.508T>C (p.Phe170Leu) c.277+1597T>C (n.277+1597T>C) c.*809T>C (n.*809T>C) c.1765T>C (p.Phe589Leu) | |
| 16 | g.89935175T>G | CA397475198 | TUBB3 | c.724T>G (p.Phe242Val) n.4145T>G c.508T>G (p.Phe170Val) c.277+1597T>G (n.277+1597T>G) c.*809T>G (n.*809T>G) c.1765T>G (p.Phe589Val) | |
| 16 | g.89935176dup | CA2808106645 | TUBB3 | c.725dup (p.Gln245ProfsTer5) n.4146dup c.509dup (p.Gln173ProfsTer5) c.277+1598dup (n.277+1598dup) c.*810dup (n.*810dup) c.1766dup (p.Gln592ProfsTer5) | |
| 16 | g.89935176T>A | CA397475200 | TUBB3 | c.725T>A (p.Phe242Tyr) n.4146T>A c.509T>A (p.Phe170Tyr) c.277+1598T>A (n.277+1598T>A) c.*810T>A (n.*810T>A) c.1766T>A (p.Phe589Tyr) | |
| 16 | g.89935176T>C | CA397475201 | TUBB3 | c.725T>C (p.Phe242Ser) n.4146T>C c.509T>C (p.Phe170Ser) c.277+1598T>C (n.277+1598T>C) c.*810T>C (n.*810T>C) c.1766T>C (p.Phe589Ser) | |
| 16 | g.89935176T>G | CA397475202 | TUBB3 | c.725T>G (p.Phe242Cys) n.4146T>G c.509T>G (p.Phe170Cys) c.277+1598T>G (n.277+1598T>G) c.*810T>G (n.*810T>G) c.1766T>G (p.Phe589Cys) | |
| 16 | g.89935177C>A | CA397475203 | TUBB3 | c.726C>A (p.Phe242Leu) n.4147C>A c.510C>A (p.Phe170Leu) c.277+1599C>A (n.277+1599C>A) c.*811C>A (n.*811C>A) c.1767C>A (p.Phe589Leu) | |
| 16 | g.89935177C= | CA2242020013 | TUBB3 | c.726C= (p.Phe242=) n.4147C= c.510C= (p.Phe170=) c.277+1599C= (n.277+1599C=) c.*811C= (n.*811C=) c.1767C= (p.Phe589=) | |
| 16 | g.89935177C>G | CA397475204 | TUBB3 | c.726C>G (p.Phe242Leu) n.4147C>G c.510C>G (p.Phe170Leu) c.277+1599C>G (n.277+1599C>G) c.*811C>G (n.*811C>G) c.1767C>G (p.Phe589Leu) | |
| 16 | g.89935177C>T | CA497381156 | TUBB3 | c.726C>T (p.Phe242=) n.4147C>T c.510C>T (p.Phe170=) c.277+1599C>T (n.277+1599C>T) c.*811C>T (n.*811C>T) c.1767C>T (p.Phe589=) | dbSNP gnomAD v4 |
| 16 | g.89935178C>A | CA397475205 | TUBB3 | c.727C>A (p.Pro243Thr) n.4148C>A c.511C>A (p.Pro171Thr) c.277+1600C>A (n.277+1600C>A) c.*812C>A (n.*812C>A) c.1768C>A (p.Pro590Thr) | |
| 16 | g.89935178C>G | CA397475206 | TUBB3 | c.727C>G (p.Pro243Ala) n.4148C>G c.511C>G (p.Pro171Ala) c.277+1600C>G (n.277+1600C>G) c.*812C>G (n.*812C>G) c.1768C>G (p.Pro590Ala) | |
| 16 | g.89935178C>T | CA397475207 | TUBB3 | c.727C>T (p.Pro243Ser) n.4148C>T c.511C>T (p.Pro171Ser) c.277+1600C>T (n.277+1600C>T) c.*812C>T (n.*812C>T) c.1768C>T (p.Pro590Ser) | |
| 16 | g.89935179C>A | CA397475208 | TUBB3 | c.728C>A (p.Pro243Gln) n.4149C>A c.512C>A (p.Pro171Gln) c.277+1601C>A (n.277+1601C>A) c.*813C>A (n.*813C>A) c.1769C>A (p.Pro590Gln) | |
| 16 | g.89935179C= | CA2242020023 | TUBB3 | c.728C= (p.Pro243=) n.4149C= c.512C= (p.Pro171=) c.277+1601C= (n.277+1601C=) c.*813C= (n.*813C=) c.1769C= (p.Pro590=) | |
| 16 | g.89935179C>G | CA397475209 | TUBB3 | c.728C>G (p.Pro243Arg) n.4149C>G c.512C>G (p.Pro171Arg) c.277+1601C>G (n.277+1601C>G) c.*813C>G (n.*813C>G) c.1769C>G (p.Pro590Arg) | ClinVar dbSNP |
| 16 | g.89935179C>T | CA213298 | TUBB3 | c.728C>T (p.Pro243Leu) n.4149C>T c.512C>T (p.Pro171Leu) c.277+1601C>T (n.277+1601C>T) c.*813C>T (n.*813C>T) c.1769C>T (p.Pro590Leu) | ClinVar dbSNP COSMIC |
| 16 | g.89935180G>A | CA8256158 | TUBB3 | c.729G>A (p.Pro243=) n.4150G>A c.513G>A (p.Pro171=) c.277+1602G>A (n.277+1602G>A) c.*814G>A (n.*814G>A) c.1770G>A (p.Pro590=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89935180G>C | CA497381157 | TUBB3 | c.729G>C (p.Pro243=) n.4150G>C c.513G>C (p.Pro171=) c.277+1602G>C (n.277+1602G>C) c.*814G>C (n.*814G>C) c.1770G>C (p.Pro590=) | |
| 16 | g.89935180G= | CA2242020027 | TUBB3 | c.729G= (p.Pro243=) n.4150G= c.513G= (p.Pro171=) c.277+1602G= (n.277+1602G=) c.*814G= (n.*814G=) c.1770G= (p.Pro590=) | |
| 16 | g.89935180G>T | CA497381159 | TUBB3 | c.729G>T (p.Pro243=) n.4150G>T c.513G>T (p.Pro171=) c.277+1602G>T (n.277+1602G>T) c.*814G>T (n.*814G>T) c.1770G>T (p.Pro590=) | |
| 16 | g.89935181G>A | CA397475210 | TUBB3 | c.730G>A (p.Gly244Ser) n.4151G>A c.514G>A (p.Gly172Ser) c.277+1603G>A (n.277+1603G>A) c.*815G>A (n.*815G>A) c.1771G>A (p.Gly591Ser) | |
| 16 | g.89935181G>C | CA397475211 | TUBB3 | c.730G>C (p.Gly244Arg) n.4151G>C c.514G>C (p.Gly172Arg) c.277+1603G>C (n.277+1603G>C) c.*815G>C (n.*815G>C) c.1771G>C (p.Gly591Arg) | |
| 16 | g.89935181G= | CA2242020031 | TUBB3 | c.730G= (p.Gly244=) n.4151G= c.514G= (p.Gly172=) c.277+1603G= (n.277+1603G=) c.*815G= (n.*815G=) c.1771G= (p.Gly591=) | |
| 16 | g.89935181G>T | CA397475212 | TUBB3 | c.730G>T (p.Gly244Cys) n.4151G>T c.514G>T (p.Gly172Cys) c.277+1603G>T (n.277+1603G>T) c.*815G>T (n.*815G>T) c.1771G>T (p.Gly591Cys) | ClinVar dbSNP COSMIC |
| 16 | g.89935182G>A | CA397475213 | TUBB3 | c.731G>A (p.Gly244Asp) n.4152G>A c.515G>A (p.Gly172Asp) c.277+1604G>A (n.277+1604G>A) c.*816G>A (n.*816G>A) c.1772G>A (p.Gly591Asp) | |
| 16 | g.89935182G>C | CA397475214 | TUBB3 | c.731G>C (p.Gly244Ala) n.4152G>C c.515G>C (p.Gly172Ala) c.277+1604G>C (n.277+1604G>C) c.*816G>C (n.*816G>C) c.1772G>C (p.Gly591Ala) | |
| 16 | g.89935182G>T | CA397475215 | TUBB3 | c.731G>T (p.Gly244Val) n.4152G>T c.515G>T (p.Gly172Val) c.277+1604G>T (n.277+1604G>T) c.*816G>T (n.*816G>T) c.1772G>T (p.Gly591Val) | |
| 16 | g.89935183C>A | CA497381162 | TUBB3 | c.732C>A (p.Gly244=) n.4153C>A c.516C>A (p.Gly172=) c.277+1605C>A (n.277+1605C>A) c.*817C>A (n.*817C>A) c.1773C>A (p.Gly591=) | |
| 16 | g.89935183C>G | CA497381164 | TUBB3 | c.732C>G (p.Gly244=) n.4153C>G c.516C>G (p.Gly172=) c.277+1605C>G (n.277+1605C>G) c.*817C>G (n.*817C>G) c.1773C>G (p.Gly591=) | gnomAD v4 |
| 16 | g.89935183C>T | CA497381163 | TUBB3 | c.732C>T (p.Gly244=) n.4153C>T c.516C>T (p.Gly172=) c.277+1605C>T (n.277+1605C>T) c.*817C>T (n.*817C>T) c.1773C>T (p.Gly591=) | COSMIC |
| 16 | g.89935184C>A | CA397475216 | TUBB3 | c.733C>A (p.Gln245Lys) n.4154C>A c.517C>A (p.Gln173Lys) c.277+1606C>A (n.277+1606C>A) c.*818C>A (n.*818C>A) c.1774C>A (p.Gln592Lys) | |
| 16 | g.89935184C= | CA2242020035 | TUBB3 | c.733C= (p.Gln245=) n.4154C= c.517C= (p.Gln173=) c.277+1606C= (n.277+1606C=) c.*818C= (n.*818C=) c.1774C= (p.Gln592=) | |
| 16 | g.89935184C>G | CA397475217 | TUBB3 | c.733C>G (p.Gln245Glu) n.4154C>G c.517C>G (p.Gln173Glu) c.277+1606C>G (n.277+1606C>G) c.*818C>G (n.*818C>G) c.1774C>G (p.Gln592Glu) | |
| 16 | g.89935184C>T | CA397475218 | TUBB3 | c.733C>T (p.Gln245Ter) n.4154C>T c.517C>T (p.Gln173Ter) c.277+1606C>T (n.277+1606C>T) c.*818C>T (n.*818C>T) c.1774C>T (p.Gln592Ter) | dbSNP gnomAD v2 gnomAD v4 |
| 16 | g.89935185A>C | CA397475219 | TUBB3 | c.734A>C (p.Gln245Pro) n.4155A>C c.518A>C (p.Gln173Pro) c.277+1607A>C (n.277+1607A>C) c.*819A>C (n.*819A>C) c.1775A>C (p.Gln592Pro) | |
| 16 | g.89935185A>G | CA397475220 | TUBB3 | c.734A>G (p.Gln245Arg) n.4155A>G c.518A>G (p.Gln173Arg) c.277+1607A>G (n.277+1607A>G) c.*819A>G (n.*819A>G) c.1775A>G (p.Gln592Arg) | |
| 16 | g.89935185A>T | CA397475221 | TUBB3 | c.734A>T (p.Gln245Leu) n.4155A>T c.518A>T (p.Gln173Leu) c.277+1607A>T (n.277+1607A>T) c.*819A>T (n.*819A>T) c.1775A>T (p.Gln592Leu) | |
| 16 | g.89935186G>A | CA497381169 | TUBB3 | c.735G>A (p.Gln245=) n.4156G>A c.519G>A (p.Gln173=) c.277+1608G>A (n.277+1608G>A) c.*820G>A (n.*820G>A) c.1776G>A (p.Gln592=) | |
| 16 | g.89935186G>C | CA397475222 | TUBB3 | c.735G>C (p.Gln245His) n.4156G>C c.519G>C (p.Gln173His) c.277+1608G>C (n.277+1608G>C) c.*820G>C (n.*820G>C) c.1776G>C (p.Gln592His) | |
| 16 | g.89935186G>T | CA397475223 | TUBB3 | c.735G>T (p.Gln245His) n.4156G>T c.519G>T (p.Gln173His) c.277+1608G>T (n.277+1608G>T) c.*820G>T (n.*820G>T) c.1776G>T (p.Gln592His) | |
| 16 | g.89935187C>A | CA397475224 | TUBB3 | c.736C>A (p.Leu246Ile) n.4157C>A c.520C>A (p.Leu174Ile) c.277+1609C>A (n.277+1609C>A) c.*821C>A (n.*821C>A) c.1777C>A (p.Leu593Ile) | |
| 16 | g.89935187C>G | CA397475225 | TUBB3 | c.736C>G (p.Leu246Val) n.4157C>G c.520C>G (p.Leu174Val) c.277+1609C>G (n.277+1609C>G) c.*821C>G (n.*821C>G) c.1777C>G (p.Leu593Val) | |
| 16 | g.89935187C>T | CA397475226 | TUBB3 | c.736C>T (p.Leu246Phe) n.4157C>T c.520C>T (p.Leu174Phe) c.277+1609C>T (n.277+1609C>T) c.*821C>T (n.*821C>T) c.1777C>T (p.Leu593Phe) | |
| 16 | g.89935188T>A | CA397475227 | TUBB3 | c.737T>A (p.Leu246His) n.4158T>A c.521T>A (p.Leu174His) c.277+1610T>A (n.277+1610T>A) c.*822T>A (n.*822T>A) c.1778T>A (p.Leu593His) | |
| 16 | g.89935188T>C | CA397475228 | TUBB3 | c.737T>C (p.Leu246Pro) n.4158T>C c.521T>C (p.Leu174Pro) c.277+1610T>C (n.277+1610T>C) c.*822T>C (n.*822T>C) c.1778T>C (p.Leu593Pro) | |
| 16 | g.89935188T>G | CA397475229 | TUBB3 | c.737T>G (p.Leu246Arg) n.4158T>G c.521T>G (p.Leu174Arg) c.277+1610T>G (n.277+1610T>G) c.*822T>G (n.*822T>G) c.1778T>G (p.Leu593Arg) | |
| 16 | g.89935189C>A | CA497381172 | TUBB3 | c.738C>A (p.Leu246=) n.4159C>A c.522C>A (p.Leu174=) c.277+1611C>A (n.277+1611C>A) c.*823C>A (n.*823C>A) c.1779C>A (p.Leu593=) | |
| 16 | g.89935189C>G | CA497381173 | TUBB3 | c.738C>G (p.Leu246=) n.4159C>G c.522C>G (p.Leu174=) c.277+1611C>G (n.277+1611C>G) c.*823C>G (n.*823C>G) c.1779C>G (p.Leu593=) | |
| 16 | g.89935189C>T | CA497381175 | TUBB3 | c.738C>T (p.Leu246=) n.4159C>T c.522C>T (p.Leu174=) c.277+1611C>T (n.277+1611C>T) c.*823C>T (n.*823C>T) c.1779C>T (p.Leu593=) | gnomAD v4 |
| 16 | g.89935190A>C | CA397475230 | TUBB3 | c.739A>C (p.Asn247His) n.4160A>C c.523A>C (p.Asn175His) c.277+1612A>C (n.277+1612A>C) c.*824A>C (n.*824A>C) c.1780A>C (p.Asn594His) | |
| 16 | g.89935190A>G | CA397475231 | TUBB3 | c.739A>G (p.Asn247Asp) n.4160A>G c.523A>G (p.Asn175Asp) c.277+1612A>G (n.277+1612A>G) c.*824A>G (n.*824A>G) c.1780A>G (p.Asn594Asp) | |
| 16 | g.89935190A>T | CA397475232 | TUBB3 | c.739A>T (p.Asn247Tyr) n.4160A>T c.523A>T (p.Asn175Tyr) c.277+1612A>T (n.277+1612A>T) c.*824A>T (n.*824A>T) c.1780A>T (p.Asn594Tyr) | |
| 16 | g.89935191A= | CA2242020040 | TUBB3 | c.740A= (p.Asn247=) n.4161A= c.524A= (p.Asn175=) c.277+1613A= (n.277+1613A=) c.*825A= (n.*825A=) c.1781A= (p.Asn594=) | |
| 16 | g.89935191A>C | CA397475233 | TUBB3 | c.740A>C (p.Asn247Thr) n.4161A>C c.524A>C (p.Asn175Thr) c.277+1613A>C (n.277+1613A>C) c.*825A>C (n.*825A>C) c.1781A>C (p.Asn594Thr) | |
| 16 | g.89935191A>G | CA213301 | TUBB3 | c.740A>G (p.Asn247Ser) n.4161A>G c.524A>G (p.Asn175Ser) c.277+1613A>G (n.277+1613A>G) c.*825A>G (n.*825A>G) c.1781A>G (p.Asn594Ser) | ClinVar dbSNP |
| 16 | g.89935191A>T | CA397475234 | TUBB3 | c.740A>T (p.Asn247Ile) n.4161A>T c.524A>T (p.Asn175Ile) c.277+1613A>T (n.277+1613A>T) c.*825A>T (n.*825A>T) c.1781A>T (p.Asn594Ile) | |
| 16 | g.89935192C>A | CA397475236 | TUBB3 | c.741C>A (p.Asn247Lys) n.4162C>A c.525C>A (p.Asn175Lys) c.277+1614C>A (n.277+1614C>A) c.*826C>A (n.*826C>A) c.1782C>A (p.Asn594Lys) | |
| 16 | g.89935192C= | CA2242020045 | TUBB3 | c.741C= (p.Asn247=) n.4162C= c.525C= (p.Asn175=) c.277+1614C= (n.277+1614C=) c.*826C= (n.*826C=) c.1782C= (p.Asn594=) | |
| 16 | g.89935192C>G | CA397475235 | TUBB3 | c.741C>G (p.Asn247Lys) n.4162C>G c.525C>G (p.Asn175Lys) c.277+1614C>G (n.277+1614C>G) c.*826C>G (n.*826C>G) c.1782C>G (p.Asn594Lys) | gnomAD v4 |
| 16 | g.89935192C>T | CA8256159 | TUBB3 | c.741C>T (p.Asn247=) n.4162C>T c.525C>T (p.Asn175=) c.277+1614C>T (n.277+1614C>T) c.*826C>T (n.*826C>T) c.1782C>T (p.Asn594=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89935193G>A | CA397475237 | TUBB3 | c.742G>A (p.Ala248Thr) n.4163G>A c.526G>A (p.Ala176Thr) c.277+1615G>A (n.277+1615G>A) c.*827G>A (n.*827G>A) c.1783G>A (p.Ala595Thr) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 16 | g.89935193G>C | CA397475238 | TUBB3 | c.742G>C (p.Ala248Pro) n.4163G>C c.526G>C (p.Ala176Pro) c.277+1615G>C (n.277+1615G>C) c.*827G>C (n.*827G>C) c.1783G>C (p.Ala595Pro) | |
| 16 | g.89935193G= | CA2242020049 | TUBB3 | c.742G= (p.Ala248=) n.4163G= c.526G= (p.Ala176=) c.277+1615G= (n.277+1615G=) c.*827G= (n.*827G=) c.1783G= (p.Ala595=) | |
| 16 | g.89935193G>T | CA397475239 | TUBB3 | c.742G>T (p.Ala248Ser) n.4163G>T c.526G>T (p.Ala176Ser) c.277+1615G>T (n.277+1615G>T) c.*827G>T (n.*827G>T) c.1783G>T (p.Ala595Ser) | dbSNP |
| 16 | g.89935194C>A | CA397475240 | TUBB3 | c.743C>A (p.Ala248Asp) n.4164C>A c.527C>A (p.Ala176Asp) c.277+1616C>A (n.277+1616C>A) c.*828C>A (n.*828C>A) c.1784C>A (p.Ala595Asp) | |
| 16 | g.89935194C>G | CA397475241 | TUBB3 | c.743C>G (p.Ala248Gly) n.4164C>G c.527C>G (p.Ala176Gly) c.277+1616C>G (n.277+1616C>G) c.*828C>G (n.*828C>G) c.1784C>G (p.Ala595Gly) | |
| 16 | g.89935194C>T | CA397475242 | TUBB3 | c.743C>T (p.Ala248Val) n.4164C>T c.527C>T (p.Ala176Val) c.277+1616C>T (n.277+1616C>T) c.*828C>T (n.*828C>T) c.1784C>T (p.Ala595Val) | |
| 16 | g.89935195T>A | CA497381180 | TUBB3 | c.744T>A (p.Ala248=) n.4165T>A c.528T>A (p.Ala176=) c.277+1617T>A (n.277+1617T>A) c.*829T>A (n.*829T>A) c.1785T>A (p.Ala595=) | dbSNP |
| 16 | g.89935195T>C | CA497381181 | TUBB3 | c.744T>C (p.Ala248=) n.4165T>C c.528T>C (p.Ala176=) c.277+1617T>C (n.277+1617T>C) c.*829T>C (n.*829T>C) c.1785T>C (p.Ala595=) | |
| 16 | g.89935195T>G | CA497381182 | TUBB3 | c.744T>G (p.Ala248=) n.4165T>G c.528T>G (p.Ala176=) c.277+1617T>G (n.277+1617T>G) c.*829T>G (n.*829T>G) c.1785T>G (p.Ala595=) | |
| 16 | g.89935195T= | CA2242020053 | TUBB3 | c.744T= (p.Ala248=) n.4165T= c.528T= (p.Ala176=) c.277+1617T= (n.277+1617T=) c.*829T= (n.*829T=) c.1785T= (p.Ala595=) | |
| 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=) |