| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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) |