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.89935440T>A | CA397476286 | TUBB3 | c.989T>A (p.Met330Lys) n.4410T>A c.773T>A (p.Met258Lys) c.277+1862T>A (n.277+1862T>A) c.*1074T>A (n.*1074T>A) c.2030T>A (p.Met677Lys) | |
| 16 | g.89935440T>C | CA286619279 | TUBB3 | c.989T>C (p.Met330Thr) n.4410T>C c.773T>C (p.Met258Thr) c.277+1862T>C (n.277+1862T>C) c.*1074T>C (n.*1074T>C) c.2030T>C (p.Met677Thr) | dbSNP |
| 16 | g.89935440T>G | CA397476289 | TUBB3 | c.989T>G (p.Met330Arg) n.4410T>G c.773T>G (p.Met258Arg) c.277+1862T>G (n.277+1862T>G) c.*1074T>G (n.*1074T>G) c.2030T>G (p.Met677Arg) | |
| 16 | g.89935440T= | CA2242020444 | TUBB3 | c.989T= (p.Met330=) n.4410T= c.773T= (p.Met258=) c.277+1862T= (n.277+1862T=) c.*1074T= (n.*1074T=) c.2030T= (p.Met677=) | |
| 16 | g.89935441G>A | CA397476292 | TUBB3 | c.990G>A (p.Met330Ile) n.4411G>A c.774G>A (p.Met258Ile) c.277+1863G>A (n.277+1863G>A) c.*1075G>A (n.*1075G>A) c.2031G>A (p.Met677Ile) | |
| 16 | g.89935441G>C | CA397476294 | TUBB3 | c.990G>C (p.Met330Ile) n.4411G>C c.774G>C (p.Met258Ile) c.277+1863G>C (n.277+1863G>C) c.*1075G>C (n.*1075G>C) c.2031G>C (p.Met677Ile) | |
| 16 | g.89935441G>T | CA397476296 | TUBB3 | c.990G>T (p.Met330Ile) n.4411G>T c.774G>T (p.Met258Ile) c.277+1863G>T (n.277+1863G>T) c.*1075G>T (n.*1075G>T) c.2031G>T (p.Met677Ile) | |
| 16 | g.89935442C>A | CA397476299 | TUBB3 | c.991C>A (p.Leu331Met) n.4412C>A c.775C>A (p.Leu259Met) c.277+1864C>A (n.277+1864C>A) c.*1076C>A (n.*1076C>A) c.2032C>A (p.Leu678Met) | |
| 16 | g.89935442C>G | CA397476304 | TUBB3 | c.991C>G (p.Leu331Val) n.4412C>G c.775C>G (p.Leu259Val) c.277+1864C>G (n.277+1864C>G) c.*1076C>G (n.*1076C>G) c.2032C>G (p.Leu678Val) | |
| 16 | g.89935442C>T | CA497381356 | TUBB3 | c.991C>T (p.Leu331=) n.4412C>T c.775C>T (p.Leu259=) c.277+1864C>T (n.277+1864C>T) c.*1076C>T (n.*1076C>T) c.2032C>T (p.Leu678=) | gnomAD v4 |
| 16 | g.89935443T>A | CA397476312 | TUBB3 | c.992T>A (p.Leu331Gln) n.4413T>A c.776T>A (p.Leu259Gln) c.277+1865T>A (n.277+1865T>A) c.*1077T>A (n.*1077T>A) c.2033T>A (p.Leu678Gln) | |
| 16 | g.89935443T>C | CA397476306 | TUBB3 | c.992T>C (p.Leu331Pro) n.4413T>C c.776T>C (p.Leu259Pro) c.277+1865T>C (n.277+1865T>C) c.*1077T>C (n.*1077T>C) c.2033T>C (p.Leu678Pro) | |
| 16 | g.89935443T>G | CA397476309 | TUBB3 | c.992T>G (p.Leu331Arg) n.4413T>G c.776T>G (p.Leu259Arg) c.277+1865T>G (n.277+1865T>G) c.*1077T>G (n.*1077T>G) c.2033T>G (p.Leu678Arg) | |
| 16 | g.89935444G>A | CA213304 | TUBB3 | c.993G>A (p.Leu331=) n.4414G>A c.777G>A (p.Leu259=) c.277+1866G>A (n.277+1866G>A) c.*1078G>A (n.*1078G>A) c.2034G>A (p.Leu678=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89935444G>C | CA8256193 | TUBB3 | c.993G>C (p.Leu331=) n.4414G>C c.777G>C (p.Leu259=) c.277+1866G>C (n.277+1866G>C) c.*1078G>C (n.*1078G>C) c.2034G>C (p.Leu678=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89935444G= | CA2242020450 | TUBB3 | c.993G= (p.Leu331=) n.4414G= c.777G= (p.Leu259=) c.277+1866G= (n.277+1866G=) c.*1078G= (n.*1078G=) c.2034G= (p.Leu678=) | |
| 16 | g.89935444G>T | CA497381357 | TUBB3 | c.993G>T (p.Leu331=) n.4414G>T c.777G>T (p.Leu259=) c.277+1866G>T (n.277+1866G>T) c.*1078G>T (n.*1078G>T) c.2034G>T (p.Leu678=) | |
| 16 | g.89935445G>A | CA397476317 | TUBB3 | c.994G>A (p.Ala332Thr) n.4415G>A c.778G>A (p.Ala260Thr) c.277+1867G>A (n.277+1867G>A) c.*1079G>A (n.*1079G>A) c.2035G>A (p.Ala679Thr) | dbSNP |
| 16 | g.89935445G>C | CA397476320 | TUBB3 | c.994G>C (p.Ala332Pro) n.4415G>C c.778G>C (p.Ala260Pro) c.277+1867G>C (n.277+1867G>C) c.*1079G>C (n.*1079G>C) c.2035G>C (p.Ala679Pro) | |
| 16 | g.89935445G= | CA2242020454 | TUBB3 | c.994G= (p.Ala332=) n.4415G= c.778G= (p.Ala260=) c.277+1867G= (n.277+1867G=) c.*1079G= (n.*1079G=) c.2035G= (p.Ala679=) | |
| 16 | g.89935445G>T | CA397476321 | TUBB3 | c.994G>T (p.Ala332Ser) n.4415G>T c.778G>T (p.Ala260Ser) c.277+1867G>T (n.277+1867G>T) c.*1079G>T (n.*1079G>T) c.2035G>T (p.Ala679Ser) | |
| 16 | g.89935446C>A | CA397476323 | TUBB3 | c.995C>A (p.Ala332Asp) n.4416C>A c.779C>A (p.Ala260Asp) c.277+1868C>A (n.277+1868C>A) c.*1080C>A (n.*1080C>A) c.2036C>A (p.Ala679Asp) | |
| 16 | g.89935446C>G | CA397476325 | TUBB3 | c.995C>G (p.Ala332Gly) n.4416C>G c.779C>G (p.Ala260Gly) c.277+1868C>G (n.277+1868C>G) c.*1080C>G (n.*1080C>G) c.2036C>G (p.Ala679Gly) | |
| 16 | g.89935446C>T | CA397476327 | TUBB3 | c.995C>T (p.Ala332Val) n.4416C>T c.779C>T (p.Ala260Val) c.277+1868C>T (n.277+1868C>T) c.*1080C>T (n.*1080C>T) c.2036C>T (p.Ala679Val) | dbSNP |
| 16 | g.89935447C>A | CA497381364 | TUBB3 | c.996C>A (p.Ala332=) n.4417C>A c.780C>A (p.Ala260=) c.277+1869C>A (n.277+1869C>A) c.*1081C>A (n.*1081C>A) c.2037C>A (p.Ala679=) | |
| 16 | g.89935447C>G | CA497381365 | TUBB3 | c.996C>G (p.Ala332=) n.4417C>G c.780C>G (p.Ala260=) c.277+1869C>G (n.277+1869C>G) c.*1081C>G (n.*1081C>G) c.2037C>G (p.Ala679=) | |
| 16 | g.89935447C>T | CA497381367 | TUBB3 | c.996C>T (p.Ala332=) n.4417C>T c.780C>T (p.Ala260=) c.277+1869C>T (n.277+1869C>T) c.*1081C>T (n.*1081C>T) c.2037C>T (p.Ala679=) | |
| 16 | g.89935448A>C | CA397476329 | TUBB3 | c.997A>C (p.Ile333Leu) n.4418A>C c.781A>C (p.Ile261Leu) c.277+1870A>C (n.277+1870A>C) c.*1082A>C (n.*1082A>C) c.2038A>C (p.Ile680Leu) | |
| 16 | g.89935448A>G | CA397476330 | TUBB3 | c.997A>G (p.Ile333Val) n.4418A>G c.781A>G (p.Ile261Val) c.277+1870A>G (n.277+1870A>G) c.*1082A>G (n.*1082A>G) c.2038A>G (p.Ile680Val) | |
| 16 | g.89935448A>T | CA397476333 | TUBB3 | c.997A>T (p.Ile333Phe) n.4418A>T c.781A>T (p.Ile261Phe) c.277+1870A>T (n.277+1870A>T) c.*1082A>T (n.*1082A>T) c.2038A>T (p.Ile680Phe) | |
| 16 | g.89935449T>A | CA397476337 | TUBB3 | c.998T>A (p.Ile333Asn) n.4419T>A c.782T>A (p.Ile261Asn) c.277+1871T>A (n.277+1871T>A) c.*1083T>A (n.*1083T>A) c.2039T>A (p.Ile680Asn) | |
| 16 | g.89935449T>C | CA397476339 | TUBB3 | c.998T>C (p.Ile333Thr) n.4419T>C c.782T>C (p.Ile261Thr) c.277+1871T>C (n.277+1871T>C) c.*1083T>C (n.*1083T>C) c.2039T>C (p.Ile680Thr) | |
| 16 | g.89935449T>G | CA397476335 | TUBB3 | c.998T>G (p.Ile333Ser) n.4419T>G c.782T>G (p.Ile261Ser) c.277+1871T>G (n.277+1871T>G) c.*1083T>G (n.*1083T>G) c.2039T>G (p.Ile680Ser) | |
| 16 | g.89935450C>A | CA497381372 | TUBB3 | c.999C>A (p.Ile333=) n.4420C>A c.783C>A (p.Ile261=) c.277+1872C>A (n.277+1872C>A) c.*1084C>A (n.*1084C>A) c.2040C>A (p.Ile680=) | |
| 16 | g.89935450C= | CA2242020458 | TUBB3 | c.999C= (p.Ile333=) n.4420C= c.783C= (p.Ile261=) c.277+1872C= (n.277+1872C=) c.*1084C= (n.*1084C=) c.2040C= (p.Ile680=) | |
| 16 | g.89935450C>G | CA397476342 | TUBB3 | c.999C>G (p.Ile333Met) n.4420C>G c.783C>G (p.Ile261Met) c.277+1872C>G (n.277+1872C>G) c.*1084C>G (n.*1084C>G) c.2040C>G (p.Ile680Met) | |
| 16 | g.89935450C>T | CA497381376 | TUBB3 | c.999C>T (p.Ile333=) n.4420C>T c.783C>T (p.Ile261=) c.277+1872C>T (n.277+1872C>T) c.*1084C>T (n.*1084C>T) c.2040C>T (p.Ile680=) | dbSNP gnomAD v3 gnomAD v4 |
| 16 | g.89935451C>A | CA397476345 | TUBB3 | c.1000C>A (p.Gln334Lys) n.4421C>A c.784C>A (p.Gln262Lys) c.277+1873C>A (n.277+1873C>A) c.*1085C>A (n.*1085C>A) c.2041C>A (p.Gln681Lys) | |
| 16 | g.89935451C>G | CA397476348 | TUBB3 | c.1000C>G (p.Gln334Glu) n.4421C>G c.784C>G (p.Gln262Glu) c.277+1873C>G (n.277+1873C>G) c.*1085C>G (n.*1085C>G) c.2041C>G (p.Gln681Glu) | |
| 16 | g.89935451C>T | CA397476350 | TUBB3 | c.1000C>T (p.Gln334Ter) n.4421C>T c.784C>T (p.Gln262Ter) c.277+1873C>T (n.277+1873C>T) c.*1085C>T (n.*1085C>T) c.2041C>T (p.Gln681Ter) | |
| 16 | g.89935452A>C | CA397476351 | TUBB3 | c.1001A>C (p.Gln334Pro) n.4422A>C c.785A>C (p.Gln262Pro) c.277+1874A>C (n.277+1874A>C) c.*1086A>C (n.*1086A>C) c.2042A>C (p.Gln681Pro) | |
| 16 | g.89935452A>G | CA397476353 | TUBB3 | c.1001A>G (p.Gln334Arg) n.4422A>G c.785A>G (p.Gln262Arg) c.277+1874A>G (n.277+1874A>G) c.*1086A>G (n.*1086A>G) c.2042A>G (p.Gln681Arg) | ClinVar |
| 16 | g.89935452A>T | CA397476355 | TUBB3 | c.1001A>T (p.Gln334Leu) n.4422A>T c.785A>T (p.Gln262Leu) c.277+1874A>T (n.277+1874A>T) c.*1086A>T (n.*1086A>T) c.2042A>T (p.Gln681Leu) | |
| 16 | g.89935453G>A | CA497381379 | TUBB3 | c.1002G>A (p.Gln334=) n.4423G>A c.786G>A (p.Gln262=) c.277+1875G>A (n.277+1875G>A) c.*1087G>A (n.*1087G>A) c.2043G>A (p.Gln681=) | |
| 16 | g.89935453G>C | CA397476358 | TUBB3 | c.1002G>C (p.Gln334His) n.4423G>C c.786G>C (p.Gln262His) c.277+1875G>C (n.277+1875G>C) c.*1087G>C (n.*1087G>C) c.2043G>C (p.Gln681His) | |
| 16 | g.89935453G>T | CA397476361 | TUBB3 | c.1002G>T (p.Gln334His) n.4423G>T c.786G>T (p.Gln262His) c.277+1875G>T (n.277+1875G>T) c.*1087G>T (n.*1087G>T) c.2043G>T (p.Gln681His) | |
| 16 | g.89935454A>C | CA397476369 | TUBB3 | c.1003A>C (p.Ser335Arg) n.4424A>C c.787A>C (p.Ser263Arg) c.277+1876A>C (n.277+1876A>C) c.*1088A>C (n.*1088A>C) c.2044A>C (p.Ser682Arg) | |
| 16 | g.89935454A>G | CA397476371 | TUBB3 | c.1003A>G (p.Ser335Gly) n.4424A>G c.787A>G (p.Ser263Gly) c.277+1876A>G (n.277+1876A>G) c.*1088A>G (n.*1088A>G) c.2044A>G (p.Ser682Gly) | |
| 16 | g.89935454A>T | CA397476373 | TUBB3 | c.1003A>T (p.Ser335Cys) n.4424A>T c.787A>T (p.Ser263Cys) c.277+1876A>T (n.277+1876A>T) c.*1088A>T (n.*1088A>T) c.2044A>T (p.Ser682Cys) | |
| 16 | g.89935455G>A | CA8256194 | TUBB3 | c.1004G>A (p.Ser335Asn) n.4425G>A c.788G>A (p.Ser263Asn) c.277+1877G>A (n.277+1877G>A) c.*1089G>A (n.*1089G>A) c.2045G>A (p.Ser682Asn) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89935455G>C | CA397476375 | TUBB3 | c.1004G>C (p.Ser335Thr) n.4425G>C c.788G>C (p.Ser263Thr) c.277+1877G>C (n.277+1877G>C) c.*1089G>C (n.*1089G>C) c.2045G>C (p.Ser682Thr) | |
| 16 | g.89935455G= | CA2242020466 | TUBB3 | c.1004G= (p.Ser335=) n.4425G= c.788G= (p.Ser263=) c.277+1877G= (n.277+1877G=) c.*1089G= (n.*1089G=) c.2045G= (p.Ser682=) | |
| 16 | g.89935455G>T | CA397476378 | TUBB3 | c.1004G>T (p.Ser335Ile) n.4425G>T c.788G>T (p.Ser263Ile) c.277+1877G>T (n.277+1877G>T) c.*1089G>T (n.*1089G>T) c.2045G>T (p.Ser682Ile) | |
| 16 | g.89935456C>A | CA397476382 | TUBB3 | c.1005C>A (p.Ser335Arg) n.4426C>A c.789C>A (p.Ser263Arg) c.277+1878C>A (n.277+1878C>A) c.*1090C>A (n.*1090C>A) c.2046C>A (p.Ser682Arg) | |
| 16 | g.89935456C= | CA2242020467 | TUBB3 | c.1005C= (p.Ser335=) n.4426C= c.789C= (p.Ser263=) c.277+1878C= (n.277+1878C=) c.*1090C= (n.*1090C=) c.2046C= (p.Ser682=) | |
| 16 | g.89935456C>G | CA397476384 | TUBB3 | c.1005C>G (p.Ser335Arg) n.4426C>G c.789C>G (p.Ser263Arg) c.277+1878C>G (n.277+1878C>G) c.*1090C>G (n.*1090C>G) c.2046C>G (p.Ser682Arg) | |
| 16 | g.89935456C>T | CA497381383 | TUBB3 | c.1005C>T (p.Ser335=) n.4426C>T c.789C>T (p.Ser263=) c.277+1878C>T (n.277+1878C>T) c.*1090C>T (n.*1090C>T) c.2046C>T (p.Ser682=) | dbSNP gnomAD v4 |
| 16 | g.89935457A>C | CA397476386 | TUBB3 | c.1006A>C (p.Lys336Gln) n.4427A>C c.790A>C (p.Lys264Gln) c.277+1879A>C (n.277+1879A>C) c.*1091A>C (n.*1091A>C) c.2047A>C (p.Lys683Gln) | |
| 16 | g.89935457A>G | CA397476394 | TUBB3 | c.1006A>G (p.Lys336Glu) n.4427A>G c.790A>G (p.Lys264Glu) c.277+1879A>G (n.277+1879A>G) c.*1091A>G (n.*1091A>G) c.2047A>G (p.Lys683Glu) | |
| 16 | g.89935457A>T | CA397476397 | TUBB3 | c.1006A>T (p.Lys336Ter) n.4427A>T c.790A>T (p.Lys264Ter) c.277+1879A>T (n.277+1879A>T) c.*1091A>T (n.*1091A>T) c.2047A>T (p.Lys683Ter) | |
| 16 | g.89935458A>C | CA397476402 | TUBB3 | c.1007A>C (p.Lys336Thr) n.4428A>C c.791A>C (p.Lys264Thr) c.277+1880A>C (n.277+1880A>C) c.*1092A>C (n.*1092A>C) c.2048A>C (p.Lys683Thr) | |
| 16 | g.89935458A>G | CA397476405 | TUBB3 | c.1007A>G (p.Lys336Arg) n.4428A>G c.791A>G (p.Lys264Arg) c.277+1880A>G (n.277+1880A>G) c.*1092A>G (n.*1092A>G) c.2048A>G (p.Lys683Arg) | |
| 16 | g.89935458A>T | CA397476407 | TUBB3 | c.1007A>T (p.Lys336Met) n.4428A>T c.791A>T (p.Lys264Met) c.277+1880A>T (n.277+1880A>T) c.*1092A>T (n.*1092A>T) c.2048A>T (p.Lys683Met) | |
| 16 | g.89935459G>A | CA497381387 | TUBB3 | c.1008G>A (p.Lys336=) n.4429G>A c.792G>A (p.Lys264=) c.277+1881G>A (n.277+1881G>A) c.*1093G>A (n.*1093G>A) c.2049G>A (p.Lys683=) | |
| 16 | g.89935459G>C | CA397476408 | TUBB3 | c.1008G>C (p.Lys336Asn) n.4429G>C c.792G>C (p.Lys264Asn) c.277+1881G>C (n.277+1881G>C) c.*1093G>C (n.*1093G>C) c.2049G>C (p.Lys683Asn) | |
| 16 | g.89935459G>T | CA397476409 | TUBB3 | c.1008G>T (p.Lys336Asn) n.4429G>T c.792G>T (p.Lys264Asn) c.277+1881G>T (n.277+1881G>T) c.*1093G>T (n.*1093G>T) c.2049G>T (p.Lys683Asn) | |
| 16 | g.89935460A>C | CA397476412 | TUBB3 | c.1009A>C (p.Asn337His) n.4430A>C c.793A>C (p.Asn265His) c.277+1882A>C (n.277+1882A>C) c.*1094A>C (n.*1094A>C) c.2050A>C (p.Asn684His) | |
| 16 | g.89935460A>G | CA397476415 | TUBB3 | c.1009A>G (p.Asn337Asp) n.4430A>G c.793A>G (p.Asn265Asp) c.277+1882A>G (n.277+1882A>G) c.*1094A>G (n.*1094A>G) c.2050A>G (p.Asn684Asp) | |
| 16 | g.89935460A>T | CA397476416 | TUBB3 | c.1009A>T (p.Asn337Tyr) n.4430A>T c.793A>T (p.Asn265Tyr) c.277+1882A>T (n.277+1882A>T) c.*1094A>T (n.*1094A>T) c.2050A>T (p.Asn684Tyr) | |
| 16 | g.89935461A>C | CA397476421 | TUBB3 | c.1010A>C (p.Asn337Thr) n.4431A>C c.794A>C (p.Asn265Thr) c.277+1883A>C (n.277+1883A>C) c.*1095A>C (n.*1095A>C) c.2051A>C (p.Asn684Thr) | |
| 16 | g.89935461A>G | CA397476423 | TUBB3 | c.1010A>G (p.Asn337Ser) n.4431A>G c.794A>G (p.Asn265Ser) c.277+1883A>G (n.277+1883A>G) c.*1095A>G (n.*1095A>G) c.2051A>G (p.Asn684Ser) | |
| 16 | g.89935461A>T | CA397476419 | TUBB3 | c.1010A>T (p.Asn337Ile) n.4431A>T c.794A>T (p.Asn265Ile) c.277+1883A>T (n.277+1883A>T) c.*1095A>T (n.*1095A>T) c.2051A>T (p.Asn684Ile) | |
| 16 | g.89935462C>A | CA397476426 | TUBB3 | c.1011C>A (p.Asn337Lys) n.4432C>A c.795C>A (p.Asn265Lys) c.277+1884C>A (n.277+1884C>A) c.*1096C>A (n.*1096C>A) c.2052C>A (p.Asn684Lys) | |
| 16 | g.89935462C>G | CA397476424 | TUBB3 | c.1011C>G (p.Asn337Lys) n.4432C>G c.795C>G (p.Asn265Lys) c.277+1884C>G (n.277+1884C>G) c.*1096C>G (n.*1096C>G) c.2052C>G (p.Asn684Lys) | |
| 16 | g.89935462C>T | CA497381393 | TUBB3 | c.1011C>T (p.Asn337=) n.4432C>T c.795C>T (p.Asn265=) c.277+1884C>T (n.277+1884C>T) c.*1096C>T (n.*1096C>T) c.2052C>T (p.Asn684=) | dbSNP gnomAD v4 |
| 16 | g.89935463del | CA915940243 | TUBB3 | c.1012del (p.Ser338AlafsTer12) n.4433del c.796del (p.Ser266AlafsTer12) c.277+1885del (n.277+1885del) c.*1097del (n.*1097del) c.2053del (p.Ser685AlafsTer12) | |
| 16 | g.89935463A= | CA915940242 | TUBB3 | c.1012A= (p.Ser338=) n.4433A= c.796A= (p.Ser266=) c.277+1885A= (n.277+1885A=) c.*1097A= (n.*1097A=) c.2053A= (p.Ser685=) | |
| 16 | g.89935463A>C | CA397476428 | TUBB3 | c.1012A>C (p.Ser338Arg) n.4433A>C c.796A>C (p.Ser266Arg) c.277+1885A>C (n.277+1885A>C) c.*1097A>C (n.*1097A>C) c.2053A>C (p.Ser685Arg) | |
| 16 | g.89935463A>G | CA397476436 | TUBB3 | c.1012A>G (p.Ser338Gly) n.4433A>G c.796A>G (p.Ser266Gly) c.277+1885A>G (n.277+1885A>G) c.*1097A>G (n.*1097A>G) c.2053A>G (p.Ser685Gly) | |
| 16 | g.89935463A>T | CA397476438 | TUBB3 | c.1012A>T (p.Ser338Cys) n.4433A>T c.796A>T (p.Ser266Cys) c.277+1885A>T (n.277+1885A>T) c.*1097A>T (n.*1097A>T) c.2053A>T (p.Ser685Cys) | |
| 16 | g.89935464G>A | CA397476443 | TUBB3 | c.1013G>A (p.Ser338Asn) n.4434G>A c.797G>A (p.Ser266Asn) c.277+1886G>A (n.277+1886G>A) c.*1098G>A (n.*1098G>A) c.2054G>A (p.Ser685Asn) | ClinVar |
| 16 | g.89935464G>C | CA397476446 | TUBB3 | c.1013G>C (p.Ser338Thr) n.4434G>C c.797G>C (p.Ser266Thr) c.277+1886G>C (n.277+1886G>C) c.*1098G>C (n.*1098G>C) c.2054G>C (p.Ser685Thr) | |
| 16 | g.89935464G>T | CA397476448 | TUBB3 | c.1013G>T (p.Ser338Ile) n.4434G>T c.797G>T (p.Ser266Ile) c.277+1886G>T (n.277+1886G>T) c.*1098G>T (n.*1098G>T) c.2054G>T (p.Ser685Ile) | |
| 16 | g.89935465C>A | CA397476451 | TUBB3 | c.1014C>A (p.Ser338Arg) n.4435C>A c.798C>A (p.Ser266Arg) c.277+1887C>A (n.277+1887C>A) c.*1099C>A (n.*1099C>A) c.2055C>A (p.Ser685Arg) | |
| 16 | g.89935465C>G | CA397476453 | TUBB3 | c.1014C>G (p.Ser338Arg) n.4435C>G c.798C>G (p.Ser266Arg) c.277+1887C>G (n.277+1887C>G) c.*1099C>G (n.*1099C>G) c.2055C>G (p.Ser685Arg) | |
| 16 | g.89935465C>T | CA497381396 | TUBB3 | c.1014C>T (p.Ser338=) n.4435C>T c.798C>T (p.Ser266=) c.277+1887C>T (n.277+1887C>T) c.*1099C>T (n.*1099C>T) c.2055C>T (p.Ser685=) | dbSNP gnomAD v4 |
| 16 | g.89935466A= | CA2242020469 | TUBB3 | c.1015A= (p.Ser339=) n.4436A= c.799A= (p.Ser267=) c.277+1888A= (n.277+1888A=) c.*1100A= (n.*1100A=) c.2056A= (p.Ser686=) | |
| 16 | g.89935466A>C | CA397476457 | TUBB3 | c.1015A>C (p.Ser339Arg) n.4436A>C c.799A>C (p.Ser267Arg) c.277+1888A>C (n.277+1888A>C) c.*1100A>C (n.*1100A>C) c.2056A>C (p.Ser686Arg) | |
| 16 | g.89935466A>G | CA397476460 | TUBB3 | c.1015A>G (p.Ser339Gly) n.4436A>G c.799A>G (p.Ser267Gly) c.277+1888A>G (n.277+1888A>G) c.*1100A>G (n.*1100A>G) c.2056A>G (p.Ser686Gly) | dbSNP gnomAD v2 gnomAD v4 |
| 16 | g.89935466A>T | CA397476463 | TUBB3 | c.1015A>T (p.Ser339Cys) n.4436A>T c.799A>T (p.Ser267Cys) c.277+1888A>T (n.277+1888A>T) c.*1100A>T (n.*1100A>T) c.2056A>T (p.Ser686Cys) | |
| 16 | g.89935467G>A | CA397476468 | TUBB3 | c.1016G>A (p.Ser339Asn) n.4437G>A c.800G>A (p.Ser267Asn) c.277+1889G>A (n.277+1889G>A) c.*1101G>A (n.*1101G>A) c.2057G>A (p.Ser686Asn) | |
| 16 | g.89935467G>C | CA397476471 | TUBB3 | c.1016G>C (p.Ser339Thr) n.4437G>C c.800G>C (p.Ser267Thr) c.277+1889G>C (n.277+1889G>C) c.*1101G>C (n.*1101G>C) c.2057G>C (p.Ser686Thr) | dbSNP |
| 16 | g.89935467G>T | CA397476467 | TUBB3 | c.1016G>T (p.Ser339Ile) n.4437G>T c.800G>T (p.Ser267Ile) c.277+1889G>T (n.277+1889G>T) c.*1101G>T (n.*1101G>T) c.2057G>T (p.Ser686Ile) | gnomAD v4 |
| 16 | g.89935468C>A | CA397476473 | TUBB3 | c.1017C>A (p.Ser339Arg) n.4438C>A c.801C>A (p.Ser267Arg) c.277+1890C>A (n.277+1890C>A) c.*1102C>A (n.*1102C>A) c.2058C>A (p.Ser686Arg) | |
| 16 | g.89935468C>G | CA397476476 | TUBB3 | c.1017C>G (p.Ser339Arg) n.4438C>G c.801C>G (p.Ser267Arg) c.277+1890C>G (n.277+1890C>G) c.*1102C>G (n.*1102C>G) c.2058C>G (p.Ser686Arg) | gnomAD v4 |
| 16 | g.89935468C>T | CA497381400 | TUBB3 | c.1017C>T (p.Ser339=) n.4438C>T c.801C>T (p.Ser267=) c.277+1890C>T (n.277+1890C>T) c.*1102C>T (n.*1102C>T) c.2058C>T (p.Ser686=) | |
| 16 | g.89935469T>A | CA397476479 | TUBB3 | c.1018T>A (p.Tyr340Asn) n.4439T>A c.802T>A (p.Tyr268Asn) c.277+1891T>A (n.277+1891T>A) c.*1103T>A (n.*1103T>A) c.2059T>A (p.Tyr687Asn) | |
| 16 | g.89935469T>C | CA397476482 | TUBB3 | c.1018T>C (p.Tyr340His) n.4439T>C c.802T>C (p.Tyr268His) c.277+1891T>C (n.277+1891T>C) c.*1103T>C (n.*1103T>C) c.2059T>C (p.Tyr687His) | |
| 16 | g.89935469T>G | CA397476484 | TUBB3 | c.1018T>G (p.Tyr340Asp) n.4439T>G c.802T>G (p.Tyr268Asp) c.277+1891T>G (n.277+1891T>G) c.*1103T>G (n.*1103T>G) c.2059T>G (p.Tyr687Asp) | |
| 16 | g.89935470A>C | CA397476492 | TUBB3 | c.1019A>C (p.Tyr340Ser) n.4440A>C c.803A>C (p.Tyr268Ser) c.277+1892A>C (n.277+1892A>C) c.*1104A>C (n.*1104A>C) c.2060A>C (p.Tyr687Ser) | |
| 16 | g.89935470A>G | CA397476487 | TUBB3 | c.1019A>G (p.Tyr340Cys) n.4440A>G c.803A>G (p.Tyr268Cys) c.277+1892A>G (n.277+1892A>G) c.*1104A>G (n.*1104A>G) c.2060A>G (p.Tyr687Cys) | |
| 16 | g.89935470A>T | CA397476489 | TUBB3 | c.1019A>T (p.Tyr340Phe) n.4440A>T c.803A>T (p.Tyr268Phe) c.277+1892A>T (n.277+1892A>T) c.*1104A>T (n.*1104A>T) c.2060A>T (p.Tyr687Phe) | |
| 16 | g.89935471C>A | CA397476494 | TUBB3 | c.1020C>A (p.Tyr340Ter) n.4441C>A c.804C>A (p.Tyr268Ter) c.277+1893C>A (n.277+1893C>A) c.*1105C>A (n.*1105C>A) c.2061C>A (p.Tyr687Ter) | dbSNP |
| 16 | g.89935471C>G | CA397476497 | TUBB3 | c.1020C>G (p.Tyr340Ter) n.4441C>G c.804C>G (p.Tyr268Ter) c.277+1893C>G (n.277+1893C>G) c.*1105C>G (n.*1105C>G) c.2061C>G (p.Tyr687Ter) | |
| 16 | g.89935471C>T | CA497381404 | TUBB3 | c.1020C>T (p.Tyr340=) n.4441C>T c.804C>T (p.Tyr268=) c.277+1893C>T (n.277+1893C>T) c.*1105C>T (n.*1105C>T) c.2061C>T (p.Tyr687=) | gnomAD v4 |
| 16 | g.89935472T>A | CA397476500 | TUBB3 | c.1021T>A (p.Phe341Ile) n.4442T>A c.805T>A (p.Phe269Ile) c.277+1894T>A (n.277+1894T>A) c.*1106T>A (n.*1106T>A) c.2062T>A (p.Phe688Ile) | |
| 16 | g.89935472T>C | CA397476501 | TUBB3 | c.1021T>C (p.Phe341Leu) n.4442T>C c.805T>C (p.Phe269Leu) c.277+1894T>C (n.277+1894T>C) c.*1106T>C (n.*1106T>C) c.2062T>C (p.Phe688Leu) | |
| 16 | g.89935472T>G | CA397476504 | TUBB3 | c.1021T>G (p.Phe341Val) n.4442T>G c.805T>G (p.Phe269Val) c.277+1894T>G (n.277+1894T>G) c.*1106T>G (n.*1106T>G) c.2062T>G (p.Phe688Val) | |
| 16 | g.89935473T>A | CA397476513 | TUBB3 | c.1022T>A (p.Phe341Tyr) n.4443T>A c.806T>A (p.Phe269Tyr) c.277+1895T>A (n.277+1895T>A) c.*1107T>A (n.*1107T>A) c.2063T>A (p.Phe688Tyr) | |
| 16 | g.89935473T>C | CA397476511 | TUBB3 | c.1022T>C (p.Phe341Ser) n.4443T>C c.806T>C (p.Phe269Ser) c.277+1895T>C (n.277+1895T>C) c.*1107T>C (n.*1107T>C) c.2063T>C (p.Phe688Ser) | |
| 16 | g.89935473T>G | CA397476508 | TUBB3 | c.1022T>G (p.Phe341Cys) n.4443T>G c.806T>G (p.Phe269Cys) c.277+1895T>G (n.277+1895T>G) c.*1107T>G (n.*1107T>G) c.2063T>G (p.Phe688Cys) | |
| 16 | g.89935474C>A | CA397476516 | TUBB3 | c.1023C>A (p.Phe341Leu) n.4444C>A c.807C>A (p.Phe269Leu) c.277+1896C>A (n.277+1896C>A) c.*1108C>A (n.*1108C>A) c.2064C>A (p.Phe688Leu) | |
| 16 | g.89935474C= | CA2242020472 | TUBB3 | c.1023C= (p.Phe341=) n.4444C= c.807C= (p.Phe269=) c.277+1896C= (n.277+1896C=) c.*1108C= (n.*1108C=) c.2064C= (p.Phe688=) | |
| 16 | g.89935474C>G | CA397476518 | TUBB3 | c.1023C>G (p.Phe341Leu) n.4444C>G c.807C>G (p.Phe269Leu) c.277+1896C>G (n.277+1896C>G) c.*1108C>G (n.*1108C>G) c.2064C>G (p.Phe688Leu) | |
| 16 | g.89935474C>T | CA8256195 | TUBB3 | c.1023C>T (p.Phe341=) n.4444C>T c.807C>T (p.Phe269=) c.277+1896C>T (n.277+1896C>T) c.*1108C>T (n.*1108C>T) c.2064C>T (p.Phe688=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 16 | g.89935475G>A | CA397476523 | TUBB3 | c.1024G>A (p.Val342Met) n.4445G>A c.808G>A (p.Val270Met) c.277+1897G>A (n.277+1897G>A) c.*1109G>A (n.*1109G>A) c.2065G>A (p.Val689Met) | ClinVar dbSNP gnomAD v4 |
| 16 | g.89935475G>C | CA397476525 | TUBB3 | c.1024G>C (p.Val342Leu) n.4445G>C c.808G>C (p.Val270Leu) c.277+1897G>C (n.277+1897G>C) c.*1109G>C (n.*1109G>C) c.2065G>C (p.Val689Leu) | |
| 16 | g.89935475G= | CA2242020475 | TUBB3 | c.1024G= (p.Val342=) n.4445G= c.808G= (p.Val270=) c.277+1897G= (n.277+1897G=) c.*1109G= (n.*1109G=) c.2065G= (p.Val689=) | |
| 16 | g.89935475G>T | CA397476528 | TUBB3 | c.1024G>T (p.Val342Leu) n.4445G>T c.808G>T (p.Val270Leu) c.277+1897G>T (n.277+1897G>T) c.*1109G>T (n.*1109G>T) c.2065G>T (p.Val689Leu) | |
| 16 | g.89935476T>A | CA397476531 | TUBB3 | c.1025T>A (p.Val342Glu) n.4446T>A c.809T>A (p.Val270Glu) c.277+1898T>A (n.277+1898T>A) c.*1110T>A (n.*1110T>A) c.2066T>A (p.Val689Glu) | |
| 16 | g.89935476T>C | CA397476533 | TUBB3 | c.1025T>C (p.Val342Ala) n.4446T>C c.809T>C (p.Val270Ala) c.277+1898T>C (n.277+1898T>C) c.*1110T>C (n.*1110T>C) c.2066T>C (p.Val689Ala) | |
| 16 | g.89935476T>G | CA397476536 | TUBB3 | c.1025T>G (p.Val342Gly) n.4446T>G c.809T>G (p.Val270Gly) c.277+1898T>G (n.277+1898T>G) c.*1110T>G (n.*1110T>G) c.2066T>G (p.Val689Gly) | |
| 16 | g.89935477G>A | CA497381410 | TUBB3 | c.1026G>A (p.Val342=) n.4447G>A c.810G>A (p.Val270=) c.277+1899G>A (n.277+1899G>A) c.*1111G>A (n.*1111G>A) c.2067G>A (p.Val689=) | |
| 16 | g.89935477G>C | CA497381411 | TUBB3 | c.1026G>C (p.Val342=) n.4447G>C c.810G>C (p.Val270=) c.277+1899G>C (n.277+1899G>C) c.*1111G>C (n.*1111G>C) c.2067G>C (p.Val689=) | |
| 16 | g.89935477G>T | CA497381412 | TUBB3 | c.1026G>T (p.Val342=) n.4447G>T c.810G>T (p.Val270=) c.277+1899G>T (n.277+1899G>T) c.*1111G>T (n.*1111G>T) c.2067G>T (p.Val689=) | |
| 16 | g.89935478G>A | CA397476538 | TUBB3 | c.1027G>A (p.Glu343Lys) n.4448G>A c.811G>A (p.Glu271Lys) c.277+1900G>A (n.277+1900G>A) c.*1112G>A (n.*1112G>A) c.2068G>A (p.Glu690Lys) | |
| 16 | g.89935478G>C | CA397476541 | TUBB3 | c.1027G>C (p.Glu343Gln) n.4448G>C c.811G>C (p.Glu271Gln) c.277+1900G>C (n.277+1900G>C) c.*1112G>C (n.*1112G>C) c.2068G>C (p.Glu690Gln) | |
| 16 | g.89935478G>T | CA397476543 | TUBB3 | c.1027G>T (p.Glu343Ter) n.4448G>T c.811G>T (p.Glu271Ter) c.277+1900G>T (n.277+1900G>T) c.*1112G>T (n.*1112G>T) c.2068G>T (p.Glu690Ter) | COSMIC |
| 16 | g.89935479A>C | CA397476548 | TUBB3 | c.1028A>C (p.Glu343Ala) n.4449A>C c.812A>C (p.Glu271Ala) c.277+1901A>C (n.277+1901A>C) c.*1113A>C (n.*1113A>C) c.2069A>C (p.Glu690Ala) | |
| 16 | g.89935479A>G | CA397476551 | TUBB3 | c.1028A>G (p.Glu343Gly) n.4449A>G c.812A>G (p.Glu271Gly) c.277+1901A>G (n.277+1901A>G) c.*1113A>G (n.*1113A>G) c.2069A>G (p.Glu690Gly) | |
| 16 | g.89935479A>T | CA397476545 | TUBB3 | c.1028A>T (p.Glu343Val) n.4449A>T c.812A>T (p.Glu271Val) c.277+1901A>T (n.277+1901A>T) c.*1113A>T (n.*1113A>T) c.2069A>T (p.Glu690Val) | |
| 16 | g.89935480G>A | CA497381413 | TUBB3 | c.1029G>A (p.Glu343=) n.4450G>A c.813G>A (p.Glu271=) c.277+1902G>A (n.277+1902G>A) c.*1114G>A (n.*1114G>A) c.2070G>A (p.Glu690=) | |
| 16 | g.89935480G>C | CA397476554 | TUBB3 | c.1029G>C (p.Glu343Asp) n.4450G>C c.813G>C (p.Glu271Asp) c.277+1902G>C (n.277+1902G>C) c.*1114G>C (n.*1114G>C) c.2070G>C (p.Glu690Asp) | |
| 16 | g.89935480G>T | CA397476556 | TUBB3 | c.1029G>T (p.Glu343Asp) n.4450G>T c.813G>T (p.Glu271Asp) c.277+1902G>T (n.277+1902G>T) c.*1114G>T (n.*1114G>T) c.2070G>T (p.Glu690Asp) | |
| 16 | g.89935481T>A | CA397476558 | TUBB3 | c.1030T>A (p.Trp344Arg) n.4451T>A c.814T>A (p.Trp272Arg) c.277+1903T>A (n.277+1903T>A) c.*1115T>A (n.*1115T>A) c.2071T>A (p.Trp691Arg) | |
| 16 | g.89935481T>C | CA397476560 | TUBB3 | c.1030T>C (p.Trp344Arg) n.4451T>C c.814T>C (p.Trp272Arg) c.277+1903T>C (n.277+1903T>C) c.*1115T>C (n.*1115T>C) c.2071T>C (p.Trp691Arg) | |
| 16 | g.89935481T>G | CA397476561 | TUBB3 | c.1030T>G (p.Trp344Gly) n.4451T>G c.814T>G (p.Trp272Gly) c.277+1903T>G (n.277+1903T>G) c.*1115T>G (n.*1115T>G) c.2071T>G (p.Trp691Gly) | |
| 16 | g.89935482G>A | CA397476564 | TUBB3 | c.1031G>A (p.Trp344Ter) n.4452G>A c.815G>A (p.Trp272Ter) c.277+1904G>A (n.277+1904G>A) c.*1116G>A (n.*1116G>A) c.2072G>A (p.Trp691Ter) | ClinVar |
| 16 | g.89935482G>C | CA397476562 | TUBB3 | c.1031G>C (p.Trp344Ser) n.4452G>C c.815G>C (p.Trp272Ser) c.277+1904G>C (n.277+1904G>C) c.*1116G>C (n.*1116G>C) c.2072G>C (p.Trp691Ser) | |
| 16 | g.89935482G>T | CA397476563 | TUBB3 | c.1031G>T (p.Trp344Leu) n.4452G>T c.815G>T (p.Trp272Leu) c.277+1904G>T (n.277+1904G>T) c.*1116G>T (n.*1116G>T) c.2072G>T (p.Trp691Leu) | |
| 16 | g.89935483G>A | CA397476565 | TUBB3 | c.1032G>A (p.Trp344Ter) n.4453G>A c.816G>A (p.Trp272Ter) c.277+1905G>A (n.277+1905G>A) c.*1117G>A (n.*1117G>A) c.2073G>A (p.Trp691Ter) | dbSNP |
| 16 | g.89935483G>C | CA397476566 | TUBB3 | c.1032G>C (p.Trp344Cys) n.4453G>C c.816G>C (p.Trp272Cys) c.277+1905G>C (n.277+1905G>C) c.*1117G>C (n.*1117G>C) c.2073G>C (p.Trp691Cys) | |
| 16 | g.89935483G>T | CA397476567 | TUBB3 | c.1032G>T (p.Trp344Cys) n.4453G>T c.816G>T (p.Trp272Cys) c.277+1905G>T (n.277+1905G>T) c.*1117G>T (n.*1117G>T) c.2073G>T (p.Trp691Cys) | |
| 16 | g.89935484A>C | CA397476568 | TUBB3 | c.1033A>C (p.Ile345Leu) n.4454A>C c.817A>C (p.Ile273Leu) c.277+1906A>C (n.277+1906A>C) c.*1118A>C (n.*1118A>C) c.2074A>C (p.Ile692Leu) | |
| 16 | g.89935484A>G | CA397476569 | TUBB3 | c.1033A>G (p.Ile345Val) n.4454A>G c.817A>G (p.Ile273Val) c.277+1906A>G (n.277+1906A>G) c.*1118A>G (n.*1118A>G) c.2074A>G (p.Ile692Val) | dbSNP |
| 16 | g.89935484A>T | CA397476570 | TUBB3 | c.1033A>T (p.Ile345Phe) n.4454A>T c.817A>T (p.Ile273Phe) c.277+1906A>T (n.277+1906A>T) c.*1118A>T (n.*1118A>T) c.2074A>T (p.Ile692Phe) | |
| 16 | g.89935485T>A | CA397476572 | TUBB3 | c.1034T>A (p.Ile345Asn) n.4455T>A c.818T>A (p.Ile273Asn) c.277+1907T>A (n.277+1907T>A) c.*1119T>A (n.*1119T>A) c.2075T>A (p.Ile692Asn) | |
| 16 | g.89935485T>C | CA397476573 | TUBB3 | c.1034T>C (p.Ile345Thr) n.4455T>C c.818T>C (p.Ile273Thr) c.277+1907T>C (n.277+1907T>C) c.*1119T>C (n.*1119T>C) c.2075T>C (p.Ile692Thr) | |
| 16 | g.89935485T>G | CA397476571 | TUBB3 | c.1034T>G (p.Ile345Ser) n.4455T>G c.818T>G (p.Ile273Ser) c.277+1907T>G (n.277+1907T>G) c.*1119T>G (n.*1119T>G) c.2075T>G (p.Ile692Ser) | |
| 16 | g.89935486C>A | CA497381463 | TUBB3 | c.1035C>A (p.Ile345=) n.4456C>A c.819C>A (p.Ile273=) c.277+1908C>A (n.277+1908C>A) c.*1120C>A (n.*1120C>A) c.2076C>A (p.Ile692=) | |
| 16 | g.89935486C= | CA2242020477 | TUBB3 | c.1035C= (p.Ile345=) n.4456C= c.819C= (p.Ile273=) c.277+1908C= (n.277+1908C=) c.*1120C= (n.*1120C=) c.2076C= (p.Ile692=) | |
| 16 | g.89935486C>G | CA397476574 | TUBB3 | c.1035C>G (p.Ile345Met) n.4456C>G c.819C>G (p.Ile273Met) c.277+1908C>G (n.277+1908C>G) c.*1120C>G (n.*1120C>G) c.2076C>G (p.Ile692Met) | |
| 16 | g.89935486C>T | CA497381464 | TUBB3 | c.1035C>T (p.Ile345=) n.4456C>T c.819C>T (p.Ile273=) c.277+1908C>T (n.277+1908C>T) c.*1120C>T (n.*1120C>T) c.2076C>T (p.Ile692=) | dbSNP gnomAD v4 |
| 16 | g.89935487C>A | CA397476576 | TUBB3 | c.1036C>A (p.Pro346Thr) n.4457C>A c.820C>A (p.Pro274Thr) c.277+1909C>A (n.277+1909C>A) c.*1121C>A (n.*1121C>A) c.2077C>A (p.Pro693Thr) | |
| 16 | g.89935487C>G | CA397476575 | TUBB3 | c.1036C>G (p.Pro346Ala) n.4457C>G c.820C>G (p.Pro274Ala) c.277+1909C>G (n.277+1909C>G) c.*1121C>G (n.*1121C>G) c.2077C>G (p.Pro693Ala) | |
| 16 | g.89935487C>T | CA397476577 | TUBB3 | c.1036C>T (p.Pro346Ser) n.4457C>T c.820C>T (p.Pro274Ser) c.277+1909C>T (n.277+1909C>T) c.*1121C>T (n.*1121C>T) c.2077C>T (p.Pro693Ser) | COSMIC |
| 16 | g.89935488C>A | CA397476578 | TUBB3 | c.1037C>A (p.Pro346His) n.4458C>A c.821C>A (p.Pro274His) c.277+1910C>A (n.277+1910C>A) c.*1122C>A (n.*1122C>A) c.2078C>A (p.Pro693His) | |
| 16 | g.89935488C>G | CA397476580 | TUBB3 | c.1037C>G (p.Pro346Arg) n.4458C>G c.821C>G (p.Pro274Arg) c.277+1910C>G (n.277+1910C>G) c.*1122C>G (n.*1122C>G) c.2078C>G (p.Pro693Arg) | |
| 16 | g.89935488C>T | CA397476579 | TUBB3 | c.1037C>T (p.Pro346Leu) n.4458C>T c.821C>T (p.Pro274Leu) c.277+1910C>T (n.277+1910C>T) c.*1122C>T (n.*1122C>T) c.2078C>T (p.Pro693Leu) | COSMIC |
| 16 | g.89935489C>A | CA497381469 | TUBB3 | c.1038C>A (p.Pro346=) n.4459C>A c.822C>A (p.Pro274=) c.277+1911C>A (n.277+1911C>A) c.*1123C>A (n.*1123C>A) c.2079C>A (p.Pro693=) | |
| 16 | g.89935489C>G | CA497381471 | TUBB3 | c.1038C>G (p.Pro346=) n.4459C>G c.822C>G (p.Pro274=) c.277+1911C>G (n.277+1911C>G) c.*1123C>G (n.*1123C>G) c.2079C>G (p.Pro693=) | |
| 16 | g.89935489C>T | CA497381472 | TUBB3 | c.1038C>T (p.Pro346=) n.4459C>T c.822C>T (p.Pro274=) c.277+1911C>T (n.277+1911C>T) c.*1123C>T (n.*1123C>T) c.2079C>T (p.Pro693=) | |
| 16 | g.89935490A>C | CA397476581 | TUBB3 | c.1039A>C (p.Asn347His) n.4460A>C c.823A>C (p.Asn275His) c.277+1912A>C (n.277+1912A>C) c.*1124A>C (n.*1124A>C) c.2080A>C (p.Asn694His) | |
| 16 | g.89935490A>G | CA397476582 | TUBB3 | c.1039A>G (p.Asn347Asp) n.4460A>G c.823A>G (p.Asn275Asp) c.277+1912A>G (n.277+1912A>G) c.*1124A>G (n.*1124A>G) c.2080A>G (p.Asn694Asp) | |
| 16 | g.89935490A>T | CA397476583 | TUBB3 | c.1039A>T (p.Asn347Tyr) n.4460A>T c.823A>T (p.Asn275Tyr) c.277+1912A>T (n.277+1912A>T) c.*1124A>T (n.*1124A>T) c.2080A>T (p.Asn694Tyr) | |
| 16 | g.89935491A>C | CA397476584 | TUBB3 | c.1040A>C (p.Asn347Thr) n.4461A>C c.824A>C (p.Asn275Thr) c.277+1913A>C (n.277+1913A>C) c.*1125A>C (n.*1125A>C) c.2081A>C (p.Asn694Thr) | |
| 16 | g.89935491A>G | CA397476585 | TUBB3 | c.1040A>G (p.Asn347Ser) n.4461A>G c.824A>G (p.Asn275Ser) c.277+1913A>G (n.277+1913A>G) c.*1125A>G (n.*1125A>G) c.2081A>G (p.Asn694Ser) | gnomAD v4 |
| 16 | g.89935491A>T | CA397476586 | TUBB3 | c.1040A>T (p.Asn347Ile) n.4461A>T c.824A>T (p.Asn275Ile) c.277+1913A>T (n.277+1913A>T) c.*1125A>T (n.*1125A>T) c.2081A>T (p.Asn694Ile) | |
| 16 | g.89935492C>A | CA397476587 | TUBB3 | c.1041C>A (p.Asn347Lys) n.4462C>A c.825C>A (p.Asn275Lys) c.277+1914C>A (n.277+1914C>A) c.*1126C>A (n.*1126C>A) c.2082C>A (p.Asn694Lys) | gnomAD v4 |
| 16 | g.89935492C>G | CA397476588 | TUBB3 | c.1041C>G (p.Asn347Lys) n.4462C>G c.825C>G (p.Asn275Lys) c.277+1914C>G (n.277+1914C>G) c.*1126C>G (n.*1126C>G) c.2082C>G (p.Asn694Lys) | |
| 16 | g.89935492C>T | CA497381475 | TUBB3 | c.1041C>T (p.Asn347=) n.4462C>T c.825C>T (p.Asn275=) c.277+1914C>T (n.277+1914C>T) c.*1126C>T (n.*1126C>T) c.2082C>T (p.Asn694=) | |
| 16 | g.89935493A>C | CA397476589 | TUBB3 | c.1042A>C (p.Asn348His) n.4463A>C c.826A>C (p.Asn276His) c.277+1915A>C (n.277+1915A>C) c.*1127A>C (n.*1127A>C) c.2083A>C (p.Asn695His) | |
| 16 | g.89935493A>G | CA397476590 | TUBB3 | c.1042A>G (p.Asn348Asp) n.4463A>G c.826A>G (p.Asn276Asp) c.277+1915A>G (n.277+1915A>G) c.*1127A>G (n.*1127A>G) c.2083A>G (p.Asn695Asp) | |
| 16 | g.89935493A>T | CA397476591 | TUBB3 | c.1042A>T (p.Asn348Tyr) n.4463A>T c.826A>T (p.Asn276Tyr) c.277+1915A>T (n.277+1915A>T) c.*1127A>T (n.*1127A>T) c.2083A>T (p.Asn695Tyr) | |
| 16 | g.89935494A>C | CA397476592 | TUBB3 | c.1043A>C (p.Asn348Thr) n.4464A>C c.827A>C (p.Asn276Thr) c.277+1916A>C (n.277+1916A>C) c.*1128A>C (n.*1128A>C) c.2084A>C (p.Asn695Thr) | |
| 16 | g.89935494A>G | CA397476594 | TUBB3 | c.1043A>G (p.Asn348Ser) n.4464A>G c.827A>G (p.Asn276Ser) c.277+1916A>G (n.277+1916A>G) c.*1128A>G (n.*1128A>G) c.2084A>G (p.Asn695Ser) | |
| 16 | g.89935494A>T | CA397476593 | TUBB3 | c.1043A>T (p.Asn348Ile) n.4464A>T c.827A>T (p.Asn276Ile) c.277+1916A>T (n.277+1916A>T) c.*1128A>T (n.*1128A>T) c.2084A>T (p.Asn695Ile) | |
| 16 | g.89935495C>A | CA397476595 | TUBB3 | c.1044C>A (p.Asn348Lys) n.4465C>A c.828C>A (p.Asn276Lys) c.277+1917C>A (n.277+1917C>A) c.*1129C>A (n.*1129C>A) c.2085C>A (p.Asn695Lys) | COSMIC |
| 16 | g.89935495C= | CA2242020481 | TUBB3 | c.1044C= (p.Asn348=) n.4465C= c.828C= (p.Asn276=) c.277+1917C= (n.277+1917C=) c.*1129C= (n.*1129C=) c.2085C= (p.Asn695=) | |
| 16 | g.89935495C>G | CA397476596 | TUBB3 | c.1044C>G (p.Asn348Lys) n.4465C>G c.828C>G (p.Asn276Lys) c.277+1917C>G (n.277+1917C>G) c.*1129C>G (n.*1129C>G) c.2085C>G (p.Asn695Lys) | |
| 16 | g.89935495C>T | CA8256196 | TUBB3 | c.1044C>T (p.Asn348=) n.4465C>T c.828C>T (p.Asn276=) c.277+1917C>T (n.277+1917C>T) c.*1129C>T (n.*1129C>T) c.2085C>T (p.Asn695=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 16 | g.89935496G>A | CA397476597 | TUBB3 | c.1045G>A (p.Val349Met) n.4466G>A c.829G>A (p.Val277Met) c.277+1918G>A (n.277+1918G>A) c.*1130G>A (n.*1130G>A) c.2086G>A (p.Val696Met) | dbSNP gnomAD v3 gnomAD v4 |
| 16 | g.89935496G>C | CA397476598 | TUBB3 | c.1045G>C (p.Val349Leu) n.4466G>C c.829G>C (p.Val277Leu) c.277+1918G>C (n.277+1918G>C) c.*1130G>C (n.*1130G>C) c.2086G>C (p.Val696Leu) | |
| 16 | g.89935496G= | CA2242020488 | TUBB3 | c.1045G= (p.Val349=) n.4466G= c.829G= (p.Val277=) c.277+1918G= (n.277+1918G=) c.*1130G= (n.*1130G=) c.2086G= (p.Val696=) | |
| 16 | g.89935496G>T | CA397476599 | TUBB3 | c.1045G>T (p.Val349Leu) n.4466G>T c.829G>T (p.Val277Leu) c.277+1918G>T (n.277+1918G>T) c.*1130G>T (n.*1130G>T) c.2086G>T (p.Val696Leu) | |
| 16 | g.89935497T>A | CA397476600 | TUBB3 | c.1046T>A (p.Val349Glu) n.4467T>A c.830T>A (p.Val277Glu) c.277+1919T>A (n.277+1919T>A) c.*1131T>A (n.*1131T>A) c.2087T>A (p.Val696Glu) | |
| 16 | g.89935497T>C | CA397476601 | TUBB3 | c.1046T>C (p.Val349Ala) n.4467T>C c.830T>C (p.Val277Ala) c.277+1919T>C (n.277+1919T>C) c.*1131T>C (n.*1131T>C) c.2087T>C (p.Val696Ala) | |
| 16 | g.89935497T>G | CA397476602 | TUBB3 | c.1046T>G (p.Val349Gly) n.4467T>G c.830T>G (p.Val277Gly) c.277+1919T>G (n.277+1919T>G) c.*1131T>G (n.*1131T>G) c.2087T>G (p.Val696Gly) | |
| 16 | g.89935498del | CA2635070897 | TUBB3 | c.1047del (p.Lys350ArgfsTer?) n.4468del c.831del (p.Lys278ArgfsTer?) c.277+1920del (n.277+1920del) c.*1132del (n.*1132del) c.2088del (p.Lys697ArgfsTer?) | gnomAD v4 |
| 16 | g.89935498G>A | CA497381478 | TUBB3 | c.1047G>A (p.Val349=) n.4468G>A c.831G>A (p.Val277=) c.277+1920G>A (n.277+1920G>A) c.*1132G>A (n.*1132G>A) c.2088G>A (p.Val696=) | COSMIC |
| 16 | g.89935498G>C | CA497381479 | TUBB3 | c.1047G>C (p.Val349=) n.4468G>C c.831G>C (p.Val277=) c.277+1920G>C (n.277+1920G>C) c.*1132G>C (n.*1132G>C) c.2088G>C (p.Val696=) | |
| 16 | g.89935498G>T | CA497381480 | TUBB3 | c.1047G>T (p.Val349=) n.4468G>T c.831G>T (p.Val277=) c.277+1920G>T (n.277+1920G>T) c.*1132G>T (n.*1132G>T) c.2088G>T (p.Val696=) | |
| 16 | g.89935499A>C | CA397476604 | TUBB3 | c.1048A>C (p.Lys350Gln) n.4469A>C c.832A>C (p.Lys278Gln) c.277+1921A>C (n.277+1921A>C) c.*1133A>C (n.*1133A>C) c.2089A>C (p.Lys697Gln) | |
| 16 | g.89935499A>G | CA397476605 | TUBB3 | c.1048A>G (p.Lys350Glu) n.4469A>G c.832A>G (p.Lys278Glu) c.277+1921A>G (n.277+1921A>G) c.*1133A>G (n.*1133A>G) c.2089A>G (p.Lys697Glu) | |
| 16 | g.89935499A>T | CA397476603 | TUBB3 | c.1048A>T (p.Lys350Ter) n.4469A>T c.832A>T (p.Lys278Ter) c.277+1921A>T (n.277+1921A>T) c.*1133A>T (n.*1133A>T) c.2089A>T (p.Lys697Ter) | |
| 16 | g.89935500A>C | CA397476606 | TUBB3 | c.1049A>C (p.Lys350Thr) n.4470A>C c.833A>C (p.Lys278Thr) c.277+1922A>C (n.277+1922A>C) c.*1134A>C (n.*1134A>C) c.2090A>C (p.Lys697Thr) | |
| 16 | g.89935500A>G | CA397476607 | TUBB3 | c.1049A>G (p.Lys350Arg) n.4470A>G c.833A>G (p.Lys278Arg) c.277+1922A>G (n.277+1922A>G) c.*1134A>G (n.*1134A>G) c.2090A>G (p.Lys697Arg) | |
| 16 | g.89935500A>T | CA397476608 | TUBB3 | c.1049A>T (p.Lys350Met) n.4470A>T c.833A>T (p.Lys278Met) c.277+1922A>T (n.277+1922A>T) c.*1134A>T (n.*1134A>T) c.2090A>T (p.Lys697Met) | |
| 16 | g.89935501G>A | CA8256197 | TUBB3 | c.1050G>A (p.Lys350=) n.4471G>A c.834G>A (p.Lys278=) c.277+1923G>A (n.277+1923G>A) c.*1135G>A (n.*1135G>A) c.2091G>A (p.Lys697=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.89935501G>C | CA397476609 | TUBB3 | c.1050G>C (p.Lys350Asn) n.4471G>C c.834G>C (p.Lys278Asn) c.277+1923G>C (n.277+1923G>C) c.*1135G>C (n.*1135G>C) c.2091G>C (p.Lys697Asn) | |
| 16 | g.89935501G= | CA2242020491 | TUBB3 | c.1050G= (p.Lys350=) n.4471G= c.834G= (p.Lys278=) c.277+1923G= (n.277+1923G=) c.*1135G= (n.*1135G=) c.2091G= (p.Lys697=) | |
| 16 | g.89935501G>T | CA397476610 | TUBB3 | c.1050G>T (p.Lys350Asn) n.4471G>T c.834G>T (p.Lys278Asn) c.277+1923G>T (n.277+1923G>T) c.*1135G>T (n.*1135G>T) c.2091G>T (p.Lys697Asn) | |
| 16 | g.89935502G>A | CA397476611 | TUBB3 | c.1051G>A (p.Val351Met) n.4472G>A c.835G>A (p.Val279Met) c.277+1924G>A (n.277+1924G>A) c.*1136G>A (n.*1136G>A) c.2092G>A (p.Val698Met) | |
| 16 | g.89935502G>C | CA397476612 | TUBB3 | c.1051G>C (p.Val351Leu) n.4472G>C c.835G>C (p.Val279Leu) c.277+1924G>C (n.277+1924G>C) c.*1136G>C (n.*1136G>C) c.2092G>C (p.Val698Leu) | |
| 16 | g.89935502G>T | CA397476613 | TUBB3 | c.1051G>T (p.Val351Leu) n.4472G>T c.835G>T (p.Val279Leu) c.277+1924G>T (n.277+1924G>T) c.*1136G>T (n.*1136G>T) c.2092G>T (p.Val698Leu) | |
| 16 | g.89935505_89935510del | CA2635070898 | TUBB3 | c.1054_1059del (p.Ala352_Val353del) n.4475_4480del c.838_843del (p.Ala280_Val281del) c.277+1927_277+1932del (n.277+1927_277+1932del) c.*1139_*1144del (n.*1139_*1144del) c.2095_2100del (p.Ala699_Val700del) | gnomAD v4 |
| 16 | g.89935503T>A | CA397476614 | TUBB3 | c.1052T>A (p.Val351Glu) n.4473T>A c.836T>A (p.Val279Glu) c.277+1925T>A (n.277+1925T>A) c.*1137T>A (n.*1137T>A) c.2093T>A (p.Val698Glu) | |
| 16 | g.89935503T>C | CA397476615 | TUBB3 | c.1052T>C (p.Val351Ala) n.4473T>C c.836T>C (p.Val279Ala) c.277+1925T>C (n.277+1925T>C) c.*1137T>C (n.*1137T>C) c.2093T>C (p.Val698Ala) | |
| 16 | g.89935503T>G | CA397476616 | TUBB3 | c.1052T>G (p.Val351Gly) n.4473T>G c.836T>G (p.Val279Gly) c.277+1925T>G (n.277+1925T>G) c.*1137T>G (n.*1137T>G) c.2093T>G (p.Val698Gly) | dbSNP |
| 16 | g.89935503T= | CA2242020493 | TUBB3 | c.1052T= (p.Val351=) n.4473T= c.836T= (p.Val279=) c.277+1925T= (n.277+1925T=) c.*1137T= (n.*1137T=) c.2093T= (p.Val698=) | |
| 16 | g.89935504G>A | CA497381486 | TUBB3 | c.1053G>A (p.Val351=) n.4474G>A c.837G>A (p.Val279=) c.277+1926G>A (n.277+1926G>A) c.*1138G>A (n.*1138G>A) c.2094G>A (p.Val698=) | dbSNP gnomAD v3 gnomAD v4 |
| 16 | g.89935504G>C | CA497381487 | TUBB3 | c.1053G>C (p.Val351=) n.4474G>C c.837G>C (p.Val279=) c.277+1926G>C (n.277+1926G>C) c.*1138G>C (n.*1138G>C) c.2094G>C (p.Val698=) | |
| 16 | g.89935504G= | CA2242020495 | TUBB3 | c.1053G= (p.Val351=) n.4474G= c.837G= (p.Val279=) c.277+1926G= (n.277+1926G=) c.*1138G= (n.*1138G=) c.2094G= (p.Val698=) | |
| 16 | g.89935504G>T | CA497381488 | TUBB3 | c.1053G>T (p.Val351=) n.4474G>T c.837G>T (p.Val279=) c.277+1926G>T (n.277+1926G>T) c.*1138G>T (n.*1138G>T) c.2094G>T (p.Val698=) | |
| 16 | g.89935505G>A | CA397476619 | TUBB3 | c.1054G>A (p.Ala352Thr) n.4475G>A c.838G>A (p.Ala280Thr) c.277+1927G>A (n.277+1927G>A) c.*1139G>A (n.*1139G>A) c.2095G>A (p.Ala699Thr) | dbSNP COSMIC |
| 16 | g.89935505G>C | CA397476617 | TUBB3 | c.1054G>C (p.Ala352Pro) n.4475G>C c.838G>C (p.Ala280Pro) c.277+1927G>C (n.277+1927G>C) c.*1139G>C (n.*1139G>C) c.2095G>C (p.Ala699Pro) | |
| 16 | g.89935505G>T | CA397476618 | TUBB3 | c.1054G>T (p.Ala352Ser) n.4475G>T c.838G>T (p.Ala280Ser) c.277+1927G>T (n.277+1927G>T) c.*1139G>T (n.*1139G>T) c.2095G>T (p.Ala699Ser) | |
| 16 | g.89935506C>A | CA397476620 | TUBB3 | c.1055C>A (p.Ala352Asp) n.4476C>A c.839C>A (p.Ala280Asp) c.277+1928C>A (n.277+1928C>A) c.*1140C>A (n.*1140C>A) c.2096C>A (p.Ala699Asp) | |
| 16 | g.89935506C>G | CA397476621 | TUBB3 | c.1055C>G (p.Ala352Gly) n.4476C>G c.839C>G (p.Ala280Gly) c.277+1928C>G (n.277+1928C>G) c.*1140C>G (n.*1140C>G) c.2096C>G (p.Ala699Gly) | |
| 16 | g.89935506C>T | CA397476622 | TUBB3 | c.1055C>T (p.Ala352Val) n.4476C>T c.839C>T (p.Ala280Val) c.277+1928C>T (n.277+1928C>T) c.*1140C>T (n.*1140C>T) c.2096C>T (p.Ala699Val) | dbSNP |
| 16 | g.89935507C>A | CA497381495 | TUBB3 | c.1056C>A (p.Ala352=) n.4477C>A c.840C>A (p.Ala280=) c.277+1929C>A (n.277+1929C>A) c.*1141C>A (n.*1141C>A) c.2097C>A (p.Ala699=) | |
| 16 | g.89935507C= | CA2242020501 | TUBB3 | c.1056C= (p.Ala352=) n.4477C= c.840C= (p.Ala280=) c.277+1929C= (n.277+1929C=) c.*1141C= (n.*1141C=) c.2097C= (p.Ala699=) | |
| 16 | g.89935507C>G | CA497381496 | TUBB3 | c.1056C>G (p.Ala352=) n.4477C>G c.840C>G (p.Ala280=) c.277+1929C>G (n.277+1929C>G) c.*1141C>G (n.*1141C>G) c.2097C>G (p.Ala699=) | gnomAD v4 |
| 16 | g.89935507C>T | CA8256198 | TUBB3 | c.1056C>T (p.Ala352=) n.4477C>T c.840C>T (p.Ala280=) c.277+1929C>T (n.277+1929C>T) c.*1141C>T (n.*1141C>T) c.2097C>T (p.Ala699=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 16 | g.89935507_89935508insA | CA2808106766 | TUBB3 | c.1056_1057insA (p.Val353SerfsTer3) n.4477_4478insA c.840_841insA (p.Val281SerfsTer3) c.277+1929_277+1930insA (n.277+1929_277+1930insA) c.*1141_*1142insA (n.*1141_*1142insA) c.2097_2098insA (p.Val700SerfsTer3) | |
| 16 | g.89935508G>A | CA397476623 | TUBB3 | c.1057G>A (p.Val353Met) n.4478G>A c.841G>A (p.Val281Met) c.277+1930G>A (n.277+1930G>A) c.*1142G>A (n.*1142G>A) c.2098G>A (p.Val700Met) | ClinVar dbSNP gnomAD v4 COSMIC |
| 16 | g.89935508G>C | CA397476624 | TUBB3 | c.1057G>C (p.Val353Leu) n.4478G>C c.841G>C (p.Val281Leu) c.277+1930G>C (n.277+1930G>C) c.*1142G>C (n.*1142G>C) c.2098G>C (p.Val700Leu) | |
| 16 | g.89935508G= | CA2242020508 | TUBB3 | c.1057G= (p.Val353=) n.4478G= c.841G= (p.Val281=) c.277+1930G= (n.277+1930G=) c.*1142G= (n.*1142G=) c.2098G= (p.Val700=) | |
| 16 | g.89935508G>T | CA397476625 | TUBB3 | c.1057G>T (p.Val353Leu) n.4478G>T c.841G>T (p.Val281Leu) c.277+1930G>T (n.277+1930G>T) c.*1142G>T (n.*1142G>T) c.2098G>T (p.Val700Leu) | |
| 16 | g.89935508_89935509insAC | CA2808106771 | TUBB3 | c.1057_1058insAC (p.Val353AspfsTer?) n.4478_4479insAC c.841_842insAC (p.Val281AspfsTer?) c.277+1930_277+1931insAC (n.277+1930_277+1931insAC) c.*1142_*1143insAC (n.*1142_*1143insAC) c.2098_2099insAC (p.Val700AspfsTer?) | |
| 16 | g.89935509T>A | CA397476626 | TUBB3 | c.1058T>A (p.Val353Glu) n.4479T>A c.842T>A (p.Val281Glu) c.277+1931T>A (n.277+1931T>A) c.*1143T>A (n.*1143T>A) c.2099T>A (p.Val700Glu) | |
| 16 | g.89935509T>C | CA397476627 | TUBB3 | c.1058T>C (p.Val353Ala) n.4479T>C c.842T>C (p.Val281Ala) c.277+1931T>C (n.277+1931T>C) c.*1143T>C (n.*1143T>C) c.2099T>C (p.Val700Ala) | |
| 16 | g.89935509T>G | CA397476628 | TUBB3 | c.1058T>G (p.Val353Gly) n.4479T>G c.842T>G (p.Val281Gly) c.277+1931T>G (n.277+1931T>G) c.*1143T>G (n.*1143T>G) c.2099T>G (p.Val700Gly) | |
| 16 | g.89935510G>A | CA497381505 | TUBB3 | c.1059G>A (p.Val353=) n.4480G>A c.843G>A (p.Val281=) c.277+1932G>A (n.277+1932G>A) c.*1144G>A (n.*1144G>A) c.2100G>A (p.Val700=) | |
| 16 | g.89935510G>C | CA497381508 | TUBB3 | c.1059G>C (p.Val353=) n.4480G>C c.843G>C (p.Val281=) c.277+1932G>C (n.277+1932G>C) c.*1144G>C (n.*1144G>C) c.2100G>C (p.Val700=) | |
| 16 | g.89935510G>T | CA497381509 | TUBB3 | c.1059G>T (p.Val353=) n.4480G>T c.843G>T (p.Val281=) c.277+1932G>T (n.277+1932G>T) c.*1144G>T (n.*1144G>T) c.2100G>T (p.Val700=) | |
| 16 | g.89935510_89935511insCTC | CA2808106773 | TUBB3 | c.1059_1060insCTC (p.Val353_Cys354insLeu) n.4480_4481insCTC c.843_844insCTC (p.Val281_Cys282insLeu) c.277+1932_277+1933insCTC (n.277+1932_277+1933insCTC) c.*1144_*1145insCTC (n.*1144_*1145insCTC) c.2100_2101insCTC (p.Val700_Cys701insLeu) | |
| 16 | g.89935511T>A | CA397476629 | TUBB3 | c.1060T>A (p.Cys354Ser) n.4481T>A c.844T>A (p.Cys282Ser) c.277+1933T>A (n.277+1933T>A) c.*1145T>A (n.*1145T>A) c.2101T>A (p.Cys701Ser) | |
| 16 | g.89935511T>C | CA397476630 | TUBB3 | c.1060T>C (p.Cys354Arg) n.4481T>C c.844T>C (p.Cys282Arg) c.277+1933T>C (n.277+1933T>C) c.*1145T>C (n.*1145T>C) c.2101T>C (p.Cys701Arg) | |
| 16 | g.89935511T>G | CA397476631 | TUBB3 | c.1060T>G (p.Cys354Gly) n.4481T>G c.844T>G (p.Cys282Gly) c.277+1933T>G (n.277+1933T>G) c.*1145T>G (n.*1145T>G) c.2101T>G (p.Cys701Gly) | |
| 16 | g.89935512G>A | CA397476633 | TUBB3 | c.1061G>A (p.Cys354Tyr) n.4482G>A c.845G>A (p.Cys282Tyr) c.277+1934G>A (n.277+1934G>A) c.*1146G>A (n.*1146G>A) c.2102G>A (p.Cys701Tyr) | |
| 16 | g.89935512G>C | CA397476634 | TUBB3 | c.1061G>C (p.Cys354Ser) n.4482G>C c.845G>C (p.Cys282Ser) c.277+1934G>C (n.277+1934G>C) c.*1146G>C (n.*1146G>C) c.2102G>C (p.Cys701Ser) | |
| 16 | g.89935512G>T | CA397476632 | TUBB3 | c.1061G>T (p.Cys354Phe) n.4482G>T c.845G>T (p.Cys282Phe) c.277+1934G>T (n.277+1934G>T) c.*1146G>T (n.*1146G>T) c.2102G>T (p.Cys701Phe) | |
| 16 | g.89935513T>A | CA397476635 | TUBB3 | c.1062T>A (p.Cys354Ter) n.4483T>A c.846T>A (p.Cys282Ter) c.277+1935T>A (n.277+1935T>A) c.*1147T>A (n.*1147T>A) c.2103T>A (p.Cys701Ter) | |
| 16 | g.89935513T>C | CA286619294 | TUBB3 | c.1062T>C (p.Cys354=) n.4483T>C c.846T>C (p.Cys282=) c.277+1935T>C (n.277+1935T>C) c.*1147T>C (n.*1147T>C) c.2103T>C (p.Cys701=) | dbSNP gnomAD v2 gnomAD v4 |
| 16 | g.89935513T>G | CA397476636 | TUBB3 | c.1062T>G (p.Cys354Trp) n.4483T>G c.846T>G (p.Cys282Trp) c.277+1935T>G (n.277+1935T>G) c.*1147T>G (n.*1147T>G) c.2103T>G (p.Cys701Trp) | |
| 16 | g.89935513T= | CA2242020514 | TUBB3 | c.1062T= (p.Cys354=) n.4483T= c.846T= (p.Cys282=) c.277+1935T= (n.277+1935T=) c.*1147T= (n.*1147T=) c.2103T= (p.Cys701=) | |
| 16 | g.89935514G>A | CA397476637 | TUBB3 | c.1063G>A (p.Asp355Asn) n.4484G>A c.847G>A (p.Asp283Asn) c.277+1936G>A (n.277+1936G>A) c.*1148G>A (n.*1148G>A) c.2104G>A (p.Asp702Asn) | |
| 16 | g.89935514G>C | CA397476638 | TUBB3 | c.1063G>C (p.Asp355His) n.4484G>C c.847G>C (p.Asp283His) c.277+1936G>C (n.277+1936G>C) c.*1148G>C (n.*1148G>C) c.2104G>C (p.Asp702His) | |
| 16 | g.89935514G>T | CA397476639 | TUBB3 | c.1063G>T (p.Asp355Tyr) n.4484G>T c.847G>T (p.Asp283Tyr) c.277+1936G>T (n.277+1936G>T) c.*1148G>T (n.*1148G>T) c.2104G>T (p.Asp702Tyr) | |
| 16 | g.89935514_89935515insCT | CA2808106778 | TUBB3 | c.1063_1064insCT (p.Asp355AlafsTer?) n.4484_4485insCT c.847_848insCT (p.Asp283AlafsTer?) c.277+1936_277+1937insCT (n.277+1936_277+1937insCT) c.*1148_*1149insCT (n.*1148_*1149insCT) c.2104_2105insCT (p.Asp702AlafsTer?) | |
| 16 | g.89935515A>C | CA397476642 | TUBB3 | c.1064A>C (p.Asp355Ala) n.4485A>C c.848A>C (p.Asp283Ala) c.277+1937A>C (n.277+1937A>C) c.*1149A>C (n.*1149A>C) c.2105A>C (p.Asp702Ala) | COSMIC |
| 16 | g.89935515A>G | CA397476640 | TUBB3 | c.1064A>G (p.Asp355Gly) n.4485A>G c.848A>G (p.Asp283Gly) c.277+1937A>G (n.277+1937A>G) c.*1149A>G (n.*1149A>G) c.2105A>G (p.Asp702Gly) | |
| 16 | g.89935515A>T | CA397476641 | TUBB3 | c.1064A>T (p.Asp355Val) n.4485A>T c.848A>T (p.Asp283Val) c.277+1937A>T (n.277+1937A>T) c.*1149A>T (n.*1149A>T) c.2105A>T (p.Asp702Val) | |
| 16 | g.89935516C>A | CA397476643 | TUBB3 | c.1065C>A (p.Asp355Glu) n.4486C>A c.849C>A (p.Asp283Glu) c.277+1938C>A (n.277+1938C>A) c.*1150C>A (n.*1150C>A) c.2106C>A (p.Asp702Glu) | |
| 16 | g.89935516C>G | CA397476644 | TUBB3 | c.1065C>G (p.Asp355Glu) n.4486C>G c.849C>G (p.Asp283Glu) c.277+1938C>G (n.277+1938C>G) c.*1150C>G (n.*1150C>G) c.2106C>G (p.Asp702Glu) | |
| 16 | g.89935516C>T | CA497381519 | TUBB3 | c.1065C>T (p.Asp355=) n.4486C>T c.849C>T (p.Asp283=) c.277+1938C>T (n.277+1938C>T) c.*1150C>T (n.*1150C>T) c.2106C>T (p.Asp702=) | gnomAD v4 |
| 16 | g.89935517A>C | CA397476645 | TUBB3 | c.1066A>C (p.Ile356Leu) n.4487A>C c.850A>C (p.Ile284Leu) c.277+1939A>C (n.277+1939A>C) c.*1151A>C (n.*1151A>C) c.2107A>C (p.Ile703Leu) | |
| 16 | g.89935517A>G | CA397476646 | TUBB3 | c.1066A>G (p.Ile356Val) n.4487A>G c.850A>G (p.Ile284Val) c.277+1939A>G (n.277+1939A>G) c.*1151A>G (n.*1151A>G) c.2107A>G (p.Ile703Val) | |
| 16 | g.89935517A>T | CA397476647 | TUBB3 | c.1066A>T (p.Ile356Phe) n.4487A>T c.850A>T (p.Ile284Phe) c.277+1939A>T (n.277+1939A>T) c.*1151A>T (n.*1151A>T) c.2107A>T (p.Ile703Phe) | gnomAD v4 |
| 16 | g.89935518T>A | CA397476650 | TUBB3 | c.1067T>A (p.Ile356Asn) n.4488T>A c.851T>A (p.Ile284Asn) c.277+1940T>A (n.277+1940T>A) c.*1152T>A (n.*1152T>A) c.2108T>A (p.Ile703Asn) | |
| 16 | g.89935518T>C | CA397476648 | TUBB3 | c.1067T>C (p.Ile356Thr) n.4488T>C c.851T>C (p.Ile284Thr) c.277+1940T>C (n.277+1940T>C) c.*1152T>C (n.*1152T>C) c.2108T>C (p.Ile703Thr) | |
| 16 | g.89935518T>G | CA397476649 | TUBB3 | c.1067T>G (p.Ile356Ser) n.4488T>G c.851T>G (p.Ile284Ser) c.277+1940T>G (n.277+1940T>G) c.*1152T>G (n.*1152T>G) c.2108T>G (p.Ile703Ser) | |
| 16 | g.89935519C>A | CA497381523 | TUBB3 | c.1068C>A (p.Ile356=) n.4489C>A c.852C>A (p.Ile284=) c.277+1941C>A (n.277+1941C>A) c.*1153C>A (n.*1153C>A) c.2109C>A (p.Ile703=) | |
| 16 | g.89935519C>G | CA397476651 | TUBB3 | c.1068C>G (p.Ile356Met) n.4489C>G c.852C>G (p.Ile284Met) c.277+1941C>G (n.277+1941C>G) c.*1153C>G (n.*1153C>G) c.2109C>G (p.Ile703Met) | |
| 16 | g.89935519C>T | CA497381524 | TUBB3 | c.1068C>T (p.Ile356=) n.4489C>T c.852C>T (p.Ile284=) c.277+1941C>T (n.277+1941C>T) c.*1153C>T (n.*1153C>T) c.2109C>T (p.Ile703=) | |
| 16 | g.89935520C>A | CA397476652 | TUBB3 | c.1069C>A (p.Pro357Thr) n.4490C>A c.853C>A (p.Pro285Thr) c.277+1942C>A (n.277+1942C>A) c.*1154C>A (n.*1154C>A) c.2110C>A (p.Pro704Thr) | |
| 16 | g.89935520C>G | CA397476653 | TUBB3 | c.1069C>G (p.Pro357Ala) n.4490C>G c.853C>G (p.Pro285Ala) c.277+1942C>G (n.277+1942C>G) c.*1154C>G (n.*1154C>G) c.2110C>G (p.Pro704Ala) | |
| 16 | g.89935520C>T | CA397476654 | TUBB3 | c.1069C>T (p.Pro357Ser) n.4490C>T c.853C>T (p.Pro285Ser) c.277+1942C>T (n.277+1942C>T) c.*1154C>T (n.*1154C>T) c.2110C>T (p.Pro704Ser) | |
| 16 | g.89935521C>A | CA397476655 | TUBB3 | c.1070C>A (p.Pro357Gln) n.4491C>A c.854C>A (p.Pro285Gln) c.277+1943C>A (n.277+1943C>A) c.*1155C>A (n.*1155C>A) c.2111C>A (p.Pro704Gln) | |
| 16 | g.89935521C>G | CA397476656 | TUBB3 | c.1070C>G (p.Pro357Arg) n.4491C>G c.854C>G (p.Pro285Arg) c.277+1943C>G (n.277+1943C>G) c.*1155C>G (n.*1155C>G) c.2111C>G (p.Pro704Arg) | |
| 16 | g.89935521C>T | CA397476657 | TUBB3 | c.1070C>T (p.Pro357Leu) n.4491C>T c.854C>T (p.Pro285Leu) c.277+1943C>T (n.277+1943C>T) c.*1155C>T (n.*1155C>T) c.2111C>T (p.Pro704Leu) | ClinVar dbSNP |
| 16 | g.89935522G>A | CA8256200 | TUBB3 | c.1071G>A (p.Pro357=) n.4492G>A c.855G>A (p.Pro285=) c.277+1944G>A (n.277+1944G>A) c.*1156G>A (n.*1156G>A) c.2112G>A (p.Pro704=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89935522G>C | CA8256199 | TUBB3 | c.1071G>C (p.Pro357=) n.4492G>C c.855G>C (p.Pro285=) c.277+1944G>C (n.277+1944G>C) c.*1156G>C (n.*1156G>C) c.2112G>C (p.Pro704=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.89935522G= | CA2242020519 | TUBB3 | c.1071G= (p.Pro357=) n.4492G= c.855G= (p.Pro285=) c.277+1944G= (n.277+1944G=) c.*1156G= (n.*1156G=) c.2112G= (p.Pro704=) | |
| 16 | g.89935522G>T | CA8256201 | TUBB3 | c.1071G>T (p.Pro357=) n.4492G>T c.855G>T (p.Pro285=) c.277+1944G>T (n.277+1944G>T) c.*1156G>T (n.*1156G>T) c.2112G>T (p.Pro704=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 16 | g.89935523C>A | CA397476658 | TUBB3 | c.1072C>A (p.Pro358Thr) n.4493C>A c.856C>A (p.Pro286Thr) c.277+1945C>A (n.277+1945C>A) c.*1157C>A (n.*1157C>A) c.2113C>A (p.Pro705Thr) | |
| 16 | g.89935523C>G | CA397476659 | TUBB3 | c.1072C>G (p.Pro358Ala) n.4493C>G c.856C>G (p.Pro286Ala) c.277+1945C>G (n.277+1945C>G) c.*1157C>G (n.*1157C>G) c.2113C>G (p.Pro705Ala) | |
| 16 | g.89935523C>T | CA397476660 | TUBB3 | c.1072C>T (p.Pro358Ser) n.4493C>T c.856C>T (p.Pro286Ser) c.277+1945C>T (n.277+1945C>T) c.*1157C>T (n.*1157C>T) c.2113C>T (p.Pro705Ser) | |
| 16 | g.89935524C>A | CA397476661 | TUBB3 | c.1073C>A (p.Pro358His) n.4494C>A c.857C>A (p.Pro286His) c.277+1946C>A (n.277+1946C>A) c.*1158C>A (n.*1158C>A) c.2114C>A (p.Pro705His) | |
| 16 | g.89935524C>G | CA397476663 | TUBB3 | c.1073C>G (p.Pro358Arg) n.4494C>G c.857C>G (p.Pro286Arg) c.277+1946C>G (n.277+1946C>G) c.*1158C>G (n.*1158C>G) c.2114C>G (p.Pro705Arg) | |
| 16 | g.89935524C>T | CA397476662 | TUBB3 | c.1073C>T (p.Pro358Leu) n.4494C>T c.857C>T (p.Pro286Leu) c.277+1946C>T (n.277+1946C>T) c.*1158C>T (n.*1158C>T) c.2114C>T (p.Pro705Leu) | |
| 16 | g.89935525C>A | CA497381532 | TUBB3 | c.1074C>A (p.Pro358=) n.4495C>A c.858C>A (p.Pro286=) c.277+1947C>A (n.277+1947C>A) c.*1159C>A (n.*1159C>A) c.2115C>A (p.Pro705=) | |
| 16 | g.89935525C>G | CA497381533 | TUBB3 | c.1074C>G (p.Pro358=) n.4495C>G c.858C>G (p.Pro286=) c.277+1947C>G (n.277+1947C>G) c.*1159C>G (n.*1159C>G) c.2115C>G (p.Pro705=) | |
| 16 | g.89935525C>T | CA497381534 | TUBB3 | c.1074C>T (p.Pro358=) n.4495C>T c.858C>T (p.Pro286=) c.277+1947C>T (n.277+1947C>T) c.*1159C>T (n.*1159C>T) c.2115C>T (p.Pro705=) | |
| 16 | g.89935526C>A | CA397476664 | TUBB3 | c.1075C>A (p.Arg359Ser) n.4496C>A c.859C>A (p.Arg287Ser) c.277+1948C>A (n.277+1948C>A) c.*1160C>A (n.*1160C>A) c.2116C>A (p.Arg706Ser) | COSMIC |
| 16 | g.89935526C= | CA2242020524 | TUBB3 | c.1075C= (p.Arg359=) n.4496C= c.859C= (p.Arg287=) c.277+1948C= (n.277+1948C=) c.*1160C= (n.*1160C=) c.2116C= (p.Arg706=) | |
| 16 | g.89935526C>G | CA397476666 | TUBB3 | c.1075C>G (p.Arg359Gly) n.4496C>G c.859C>G (p.Arg287Gly) c.277+1948C>G (n.277+1948C>G) c.*1160C>G (n.*1160C>G) c.2116C>G (p.Arg706Gly) | |
| 16 | g.89935526C>T | CA397476667 | TUBB3 | c.1075C>T (p.Arg359Cys) n.4496C>T c.859C>T (p.Arg287Cys) c.277+1948C>T (n.277+1948C>T) c.*1160C>T (n.*1160C>T) c.2116C>T (p.Arg706Cys) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 16 | g.89935527G>A | CA8256202 | TUBB3 | c.1076G>A (p.Arg359His) n.4497G>A c.860G>A (p.Arg287His) c.277+1949G>A (n.277+1949G>A) c.*1161G>A (n.*1161G>A) c.2117G>A (p.Arg706His) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 16 | g.89935527G>C | CA397476668 | TUBB3 | c.1076G>C (p.Arg359Pro) n.4497G>C c.860G>C (p.Arg287Pro) c.277+1949G>C (n.277+1949G>C) c.*1161G>C (n.*1161G>C) c.2117G>C (p.Arg706Pro) | |
| 16 | g.89935527G= | CA2242020528 | TUBB3 | c.1076G= (p.Arg359=) n.4497G= c.860G= (p.Arg287=) c.277+1949G= (n.277+1949G=) c.*1161G= (n.*1161G=) c.2117G= (p.Arg706=) | |
| 16 | g.89935527G>T | CA397476669 | TUBB3 | c.1076G>T (p.Arg359Leu) n.4497G>T c.860G>T (p.Arg287Leu) c.277+1949G>T (n.277+1949G>T) c.*1161G>T (n.*1161G>T) c.2117G>T (p.Arg706Leu) | |
| 16 | g.89935528C>A | CA497381539 | TUBB3 | c.1077C>A (p.Arg359=) n.4498C>A c.861C>A (p.Arg287=) c.277+1950C>A (n.277+1950C>A) c.*1162C>A (n.*1162C>A) c.2118C>A (p.Arg706=) | gnomAD v4 |
| 16 | g.89935528C= | CA2242020532 | TUBB3 | c.1077C= (p.Arg359=) n.4498C= c.861C= (p.Arg287=) c.277+1950C= (n.277+1950C=) c.*1162C= (n.*1162C=) c.2118C= (p.Arg706=) | |
| 16 | g.89935528C>G | CA497381540 | TUBB3 | c.1077C>G (p.Arg359=) n.4498C>G c.861C>G (p.Arg287=) c.277+1950C>G (n.277+1950C>G) c.*1162C>G (n.*1162C>G) c.2118C>G (p.Arg706=) | |
| 16 | g.89935528C>T | CA8256203 | TUBB3 | c.1077C>T (p.Arg359=) n.4498C>T c.861C>T (p.Arg287=) c.277+1950C>T (n.277+1950C>T) c.*1162C>T (n.*1162C>T) c.2118C>T (p.Arg706=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 16 | g.89935529G>A | CA8256204 | TUBB3 | c.1078G>A (p.Gly360Ser) n.4499G>A c.862G>A (p.Gly288Ser) c.277+1951G>A (n.277+1951G>A) c.*1163G>A (n.*1163G>A) c.2119G>A (p.Gly707Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89935529G>C | CA397476670 | TUBB3 | c.1078G>C (p.Gly360Arg) n.4499G>C c.862G>C (p.Gly288Arg) c.277+1951G>C (n.277+1951G>C) c.*1163G>C (n.*1163G>C) c.2119G>C (p.Gly707Arg) | COSMIC |
| 16 | g.89935529G= | CA2242020535 | TUBB3 | c.1078G= (p.Gly360=) n.4499G= c.862G= (p.Gly288=) c.277+1951G= (n.277+1951G=) c.*1163G= (n.*1163G=) c.2119G= (p.Gly707=) | |
| 16 | g.89935529G>T | CA397476671 | TUBB3 | c.1078G>T (p.Gly360Cys) n.4499G>T c.862G>T (p.Gly288Cys) c.277+1951G>T (n.277+1951G>T) c.*1163G>T (n.*1163G>T) c.2119G>T (p.Gly707Cys) | |
| 16 | g.89935530del | CA2635070899 | TUBB3 | c.1079del (p.Gly360AlafsTer?) n.4500del c.863del (p.Gly288AlafsTer?) c.277+1952del (n.277+1952del) c.*1164del (n.*1164del) c.2120del (p.Gly707AlafsTer?) | gnomAD v4 |
| 16 | g.89935530G>A | CA397476672 | TUBB3 | c.1079G>A (p.Gly360Asp) n.4500G>A c.863G>A (p.Gly288Asp) c.277+1952G>A (n.277+1952G>A) c.*1164G>A (n.*1164G>A) c.2120G>A (p.Gly707Asp) | dbSNP |
| 16 | g.89935530G>C | CA397476673 | TUBB3 | c.1079G>C (p.Gly360Ala) n.4500G>C c.863G>C (p.Gly288Ala) c.277+1952G>C (n.277+1952G>C) c.*1164G>C (n.*1164G>C) c.2120G>C (p.Gly707Ala) | |
| 16 | g.89935530G>T | CA397476674 | TUBB3 | c.1079G>T (p.Gly360Val) n.4500G>T c.863G>T (p.Gly288Val) c.277+1952G>T (n.277+1952G>T) c.*1164G>T (n.*1164G>T) c.2120G>T (p.Gly707Val) | |
| 16 | g.89935531C>A | CA8256206 | TUBB3 | c.1080C>A (p.Gly360=) n.4501C>A c.864C>A (p.Gly288=) c.277+1953C>A (n.277+1953C>A) c.*1165C>A (n.*1165C>A) c.2121C>A (p.Gly707=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89935531C= | CA2242020541 | TUBB3 | c.1080C= (p.Gly360=) n.4501C= c.864C= (p.Gly288=) c.277+1953C= (n.277+1953C=) c.*1165C= (n.*1165C=) c.2121C= (p.Gly707=) | |
| 16 | g.89935531C>G | CA497381545 | TUBB3 | c.1080C>G (p.Gly360=) n.4501C>G c.864C>G (p.Gly288=) c.277+1953C>G (n.277+1953C>G) c.*1165C>G (n.*1165C>G) c.2121C>G (p.Gly707=) | dbSNP |
| 16 | g.89935531C>T | CA8256205 | TUBB3 | c.1080C>T (p.Gly360=) n.4501C>T c.864C>T (p.Gly288=) c.277+1953C>T (n.277+1953C>T) c.*1165C>T (n.*1165C>T) c.2121C>T (p.Gly707=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89935532C>A | CA16620316 | TUBB3 | c.1081C>A (p.Leu361Ile) n.4502C>A c.865C>A (p.Leu289Ile) c.277+1954C>A (n.277+1954C>A) c.*1166C>A (n.*1166C>A) c.2122C>A (p.Leu708Ile) | ClinVar dbSNP gnomAD v4 |
| 16 | g.89935532C= | CA2242020546 | TUBB3 | c.1081C= (p.Leu361=) n.4502C= c.865C= (p.Leu289=) c.277+1954C= (n.277+1954C=) c.*1166C= (n.*1166C=) c.2122C= (p.Leu708=) | |
| 16 | g.89935532C>G | CA397476675 | TUBB3 | c.1081C>G (p.Leu361Val) n.4502C>G c.865C>G (p.Leu289Val) c.277+1954C>G (n.277+1954C>G) c.*1166C>G (n.*1166C>G) c.2122C>G (p.Leu708Val) | |
| 16 | g.89935532C>T | CA397476676 | TUBB3 | c.1081C>T (p.Leu361Phe) n.4502C>T c.865C>T (p.Leu289Phe) c.277+1954C>T (n.277+1954C>T) c.*1166C>T (n.*1166C>T) c.2122C>T (p.Leu708Phe) | |
| 16 | g.89935533T>A | CA397476677 | TUBB3 | c.1082T>A (p.Leu361His) n.4503T>A c.866T>A (p.Leu289His) c.277+1955T>A (n.277+1955T>A) c.*1167T>A (n.*1167T>A) c.2123T>A (p.Leu708His) | |
| 16 | g.89935533T>C | CA397476678 | TUBB3 | c.1082T>C (p.Leu361Pro) n.4503T>C c.866T>C (p.Leu289Pro) c.277+1955T>C (n.277+1955T>C) c.*1167T>C (n.*1167T>C) c.2123T>C (p.Leu708Pro) | |
| 16 | g.89935533T>G | CA397476679 | TUBB3 | c.1082T>G (p.Leu361Arg) n.4503T>G c.866T>G (p.Leu289Arg) c.277+1955T>G (n.277+1955T>G) c.*1167T>G (n.*1167T>G) c.2123T>G (p.Leu708Arg) | |
| 16 | g.89935534C>A | CA497381550 | TUBB3 | c.1083C>A (p.Leu361=) n.4504C>A c.867C>A (p.Leu289=) c.277+1956C>A (n.277+1956C>A) c.*1168C>A (n.*1168C>A) c.2124C>A (p.Leu708=) | |
| 16 | g.89935534C= | CA2242020552 | TUBB3 | c.1083C= (p.Leu361=) n.4504C= c.867C= (p.Leu289=) c.277+1956C= (n.277+1956C=) c.*1168C= (n.*1168C=) c.2124C= (p.Leu708=) | |
| 16 | g.89935534C>G | CA286619311 | TUBB3 | c.1083C>G (p.Leu361=) n.4504C>G c.867C>G (p.Leu289=) c.277+1956C>G (n.277+1956C>G) c.*1168C>G (n.*1168C>G) c.2124C>G (p.Leu708=) | dbSNP gnomAD v3 gnomAD v4 |
| 16 | g.89935534C>T | CA497381549 | TUBB3 | c.1083C>T (p.Leu361=) n.4504C>T c.867C>T (p.Leu289=) c.277+1956C>T (n.277+1956C>T) c.*1168C>T (n.*1168C>T) c.2124C>T (p.Leu708=) | |
| 16 | g.89935535A>C | CA397476680 | TUBB3 | c.1084A>C (p.Lys362Gln) n.4505A>C c.868A>C (p.Lys290Gln) c.277+1957A>C (n.277+1957A>C) c.*1169A>C (n.*1169A>C) c.2125A>C (p.Lys709Gln) | |
| 16 | g.89935535A>G | CA397476681 | TUBB3 | c.1084A>G (p.Lys362Glu) n.4505A>G c.868A>G (p.Lys290Glu) c.277+1957A>G (n.277+1957A>G) c.*1169A>G (n.*1169A>G) c.2125A>G (p.Lys709Glu) | |
| 16 | g.89935535A>T | CA397476682 | TUBB3 | c.1084A>T (p.Lys362Ter) n.4505A>T c.868A>T (p.Lys290Ter) c.277+1957A>T (n.277+1957A>T) c.*1169A>T (n.*1169A>T) c.2125A>T (p.Lys709Ter) | |
| 16 | g.89935536A>C | CA397476683 | TUBB3 | c.1085A>C (p.Lys362Thr) n.4506A>C c.869A>C (p.Lys290Thr) c.277+1958A>C (n.277+1958A>C) c.*1170A>C (n.*1170A>C) c.2126A>C (p.Lys709Thr) | |
| 16 | g.89935536A>G | CA397476684 | TUBB3 | c.1085A>G (p.Lys362Arg) n.4506A>G c.869A>G (p.Lys290Arg) c.277+1958A>G (n.277+1958A>G) c.*1170A>G (n.*1170A>G) c.2126A>G (p.Lys709Arg) | |
| 16 | g.89935536A>T | CA397476685 | TUBB3 | c.1085A>T (p.Lys362Met) n.4506A>T c.869A>T (p.Lys290Met) c.277+1958A>T (n.277+1958A>T) c.*1170A>T (n.*1170A>T) c.2126A>T (p.Lys709Met) | |
| 16 | g.89935537G>A | CA497381555 | TUBB3 | c.1086G>A (p.Lys362=) n.4507G>A c.870G>A (p.Lys290=) c.277+1959G>A (n.277+1959G>A) c.*1171G>A (n.*1171G>A) c.2127G>A (p.Lys709=) | |
| 16 | g.89935537G>C | CA397476686 | TUBB3 | c.1086G>C (p.Lys362Asn) n.4507G>C c.870G>C (p.Lys290Asn) c.277+1959G>C (n.277+1959G>C) c.*1171G>C (n.*1171G>C) c.2127G>C (p.Lys709Asn) | dbSNP |
| 16 | g.89935537G>T | CA397476687 | TUBB3 | c.1086G>T (p.Lys362Asn) n.4507G>T c.870G>T (p.Lys290Asn) c.277+1959G>T (n.277+1959G>T) c.*1171G>T (n.*1171G>T) c.2127G>T (p.Lys709Asn) | |
| 16 | g.89935538A>C | CA397476688 | TUBB3 | c.1087A>C (p.Met363Leu) n.4508A>C c.871A>C (p.Met291Leu) c.277+1960A>C (n.277+1960A>C) c.*1172A>C (n.*1172A>C) c.2128A>C (p.Met710Leu) | |
| 16 | g.89935538A>G | CA397476690 | TUBB3 | c.1087A>G (p.Met363Val) n.4508A>G c.871A>G (p.Met291Val) c.277+1960A>G (n.277+1960A>G) c.*1172A>G (n.*1172A>G) c.2128A>G (p.Met710Val) | |
| 16 | g.89935538A>T | CA397476689 | TUBB3 | c.1087A>T (p.Met363Leu) n.4508A>T c.871A>T (p.Met291Leu) c.277+1960A>T (n.277+1960A>T) c.*1172A>T (n.*1172A>T) c.2128A>T (p.Met710Leu) | |
| 16 | g.89935539T>A | CA397476691 | TUBB3 | c.1088T>A (p.Met363Lys) n.4509T>A c.872T>A (p.Met291Lys) c.277+1961T>A (n.277+1961T>A) c.*1173T>A (n.*1173T>A) c.2129T>A (p.Met710Lys) | |
| 16 | g.89935539T>C | CA397476693 | TUBB3 | c.1088T>C (p.Met363Thr) n.4509T>C c.872T>C (p.Met291Thr) c.277+1961T>C (n.277+1961T>C) c.*1173T>C (n.*1173T>C) c.2129T>C (p.Met710Thr) | |
| 16 | g.89935539T>G | CA397476692 | TUBB3 | c.1088T>G (p.Met363Arg) n.4509T>G c.872T>G (p.Met291Arg) c.277+1961T>G (n.277+1961T>G) c.*1173T>G (n.*1173T>G) c.2129T>G (p.Met710Arg) | |
| 16 | g.89935540G>A | CA397476694 | TUBB3 | c.1089G>A (p.Met363Ile) n.4510G>A c.873G>A (p.Met291Ile) c.277+1962G>A (n.277+1962G>A) c.*1174G>A (n.*1174G>A) c.2130G>A (p.Met710Ile) | |
| 16 | g.89935540G>C | CA397476695 | TUBB3 | c.1089G>C (p.Met363Ile) n.4510G>C c.873G>C (p.Met291Ile) c.277+1962G>C (n.277+1962G>C) c.*1174G>C (n.*1174G>C) c.2130G>C (p.Met710Ile) | |
| 16 | g.89935540G>T | CA397476696 | TUBB3 | c.1089G>T (p.Met363Ile) n.4510G>T c.873G>T (p.Met291Ile) c.277+1962G>T (n.277+1962G>T) c.*1174G>T (n.*1174G>T) c.2130G>T (p.Met710Ile) |