| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.89935432C>A | CA397476252 | TUBB3 | c.981C>A (p.Asp327Glu) n.4402C>A c.765C>A (p.Asp255Glu) c.277+1854C>A (n.277+1854C>A) c.*1066C>A (n.*1066C>A) c.2022C>A (p.Asp674Glu) | |
| 16 | g.89935432C= | CA2242020434 | TUBB3 | c.981C= (p.Asp327=) n.4402C= c.765C= (p.Asp255=) c.277+1854C= (n.277+1854C=) c.*1066C= (n.*1066C=) c.2022C= (p.Asp674=) | |
| 16 | g.89935432C>G | CA397476254 | TUBB3 | c.981C>G (p.Asp327Glu) n.4402C>G c.765C>G (p.Asp255Glu) c.277+1854C>G (n.277+1854C>G) c.*1066C>G (n.*1066C>G) c.2022C>G (p.Asp674Glu) | gnomAD v3 gnomAD v4 |
| 16 | g.89935432C>T | CA8256192 | TUBB3 | c.981C>T (p.Asp327=) n.4402C>T c.765C>T (p.Asp255=) c.277+1854C>T (n.277+1854C>T) c.*1066C>T (n.*1066C>T) c.2022C>T (p.Asp674=) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 16 | g.89935433G>A | CA16043693 | TUBB3 | c.982G>A (p.Glu328Lys) n.4403G>A c.766G>A (p.Glu256Lys) c.277+1855G>A (n.277+1855G>A) c.*1067G>A (n.*1067G>A) c.2023G>A (p.Glu675Lys) | ClinVar dbSNP |
| 16 | g.89935433G>C | CA397476258 | TUBB3 | c.982G>C (p.Glu328Gln) n.4403G>C c.766G>C (p.Glu256Gln) c.277+1855G>C (n.277+1855G>C) c.*1067G>C (n.*1067G>C) c.2023G>C (p.Glu675Gln) | |
| 16 | g.89935433G= | CA2242020437 | TUBB3 | c.982G= (p.Glu328=) n.4403G= c.766G= (p.Glu256=) c.277+1855G= (n.277+1855G=) c.*1067G= (n.*1067G=) c.2023G= (p.Glu675=) | |
| 16 | g.89935433G>T | CA397476256 | TUBB3 | c.982G>T (p.Glu328Ter) n.4403G>T c.766G>T (p.Glu256Ter) c.277+1855G>T (n.277+1855G>T) c.*1067G>T (n.*1067G>T) c.2023G>T (p.Glu675Ter) | |
| 16 | g.89935434A>C | CA397476259 | TUBB3 | c.983A>C (p.Glu328Ala) n.4404A>C c.767A>C (p.Glu256Ala) c.277+1856A>C (n.277+1856A>C) c.*1068A>C (n.*1068A>C) c.2024A>C (p.Glu675Ala) | |
| 16 | g.89935434A>G | CA397476260 | TUBB3 | c.983A>G (p.Glu328Gly) n.4404A>G c.767A>G (p.Glu256Gly) c.277+1856A>G (n.277+1856A>G) c.*1068A>G (n.*1068A>G) c.2024A>G (p.Glu675Gly) | |
| 16 | g.89935434A>T | CA397476261 | TUBB3 | c.983A>T (p.Glu328Val) n.4404A>T c.767A>T (p.Glu256Val) c.277+1856A>T (n.277+1856A>T) c.*1068A>T (n.*1068A>T) c.2024A>T (p.Glu675Val) | |
| 16 | g.89935435G>A | CA497381349 | TUBB3 | c.984G>A (p.Glu328=) n.4405G>A c.768G>A (p.Glu256=) c.277+1857G>A (n.277+1857G>A) c.*1069G>A (n.*1069G>A) c.2025G>A (p.Glu675=) | |
| 16 | g.89935435G>C | CA397476262 | TUBB3 | c.984G>C (p.Glu328Asp) n.4405G>C c.768G>C (p.Glu256Asp) c.277+1857G>C (n.277+1857G>C) c.*1069G>C (n.*1069G>C) c.2025G>C (p.Glu675Asp) | gnomAD v3 gnomAD v4 |
| 16 | g.89935435G>T | CA397476263 | TUBB3 | c.984G>T (p.Glu328Asp) n.4405G>T c.768G>T (p.Glu256Asp) c.277+1857G>T (n.277+1857G>T) c.*1069G>T (n.*1069G>T) c.2025G>T (p.Glu675Asp) | |
| 16 | g.89935436C>A | CA397476267 | TUBB3 | c.985C>A (p.Gln329Lys) n.4406C>A c.769C>A (p.Gln257Lys) c.277+1858C>A (n.277+1858C>A) c.*1070C>A (n.*1070C>A) c.2026C>A (p.Gln676Lys) | dbSNP |
| 16 | g.89935436C= | CA2242020441 | TUBB3 | c.985C= (p.Gln329=) n.4406C= c.769C= (p.Gln257=) c.277+1858C= (n.277+1858C=) c.*1070C= (n.*1070C=) c.2026C= (p.Gln676=) | |
| 16 | g.89935436C>G | CA397476265 | TUBB3 | c.985C>G (p.Gln329Glu) n.4406C>G c.769C>G (p.Gln257Glu) c.277+1858C>G (n.277+1858C>G) c.*1070C>G (n.*1070C>G) c.2026C>G (p.Gln676Glu) | ClinVar |
| 16 | g.89935436C>T | CA397476264 | TUBB3 | c.985C>T (p.Gln329Ter) n.4406C>T c.769C>T (p.Gln257Ter) c.277+1858C>T (n.277+1858C>T) c.*1070C>T (n.*1070C>T) c.2026C>T (p.Gln676Ter) | gnomAD v4 |
| 16 | g.89935437A>C | CA397476270 | TUBB3 | c.986A>C (p.Gln329Pro) n.4407A>C c.770A>C (p.Gln257Pro) c.277+1859A>C (n.277+1859A>C) c.*1071A>C (n.*1071A>C) c.2027A>C (p.Gln676Pro) | |
| 16 | g.89935437A>G | CA397476268 | TUBB3 | c.986A>G (p.Gln329Arg) n.4407A>G c.770A>G (p.Gln257Arg) c.277+1859A>G (n.277+1859A>G) c.*1071A>G (n.*1071A>G) c.2027A>G (p.Gln676Arg) | |
| 16 | g.89935437A>T | CA397476271 | TUBB3 | c.986A>T (p.Gln329Leu) n.4407A>T c.770A>T (p.Gln257Leu) c.277+1859A>T (n.277+1859A>T) c.*1071A>T (n.*1071A>T) c.2027A>T (p.Gln676Leu) | |
| 16 | g.89935438G>A | CA497381351 | TUBB3 | c.987G>A (p.Gln329=) n.4408G>A c.771G>A (p.Gln257=) c.277+1860G>A (n.277+1860G>A) c.*1072G>A (n.*1072G>A) c.2028G>A (p.Gln676=) | |
| 16 | g.89935438G>C | CA397476274 | TUBB3 | c.987G>C (p.Gln329His) n.4408G>C c.771G>C (p.Gln257His) c.277+1860G>C (n.277+1860G>C) c.*1072G>C (n.*1072G>C) c.2028G>C (p.Gln676His) | gnomAD v4 |
| 16 | g.89935438G>T | CA397476275 | TUBB3 | c.987G>T (p.Gln329His) n.4408G>T c.771G>T (p.Gln257His) c.277+1860G>T (n.277+1860G>T) c.*1072G>T (n.*1072G>T) c.2028G>T (p.Gln676His) | |
| 16 | g.89935439A>C | CA397476277 | TUBB3 | c.988A>C (p.Met330Leu) n.4409A>C c.772A>C (p.Met258Leu) c.277+1861A>C (n.277+1861A>C) c.*1073A>C (n.*1073A>C) c.2029A>C (p.Met677Leu) | |
| 16 | g.89935439A>G | CA397476280 | TUBB3 | c.988A>G (p.Met330Val) n.4409A>G c.772A>G (p.Met258Val) c.277+1861A>G (n.277+1861A>G) c.*1073A>G (n.*1073A>G) c.2029A>G (p.Met677Val) | |
| 16 | g.89935439A>T | CA397476283 | TUBB3 | c.988A>T (p.Met330Leu) n.4409A>T c.772A>T (p.Met258Leu) c.277+1861A>T (n.277+1861A>T) c.*1073A>T (n.*1073A>T) c.2029A>T (p.Met677Leu) | |
| 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) |