| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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) | |
| 16 | g.89935541T>A | CA397476697 | TUBB3 | c.1090T>A (p.Ser364Thr) n.4511T>A c.874T>A (p.Ser292Thr) c.277+1963T>A (n.277+1963T>A) c.*1175T>A (n.*1175T>A) c.2131T>A (p.Ser711Thr) | gnomAD v4 |
| 16 | g.89935541T>C | CA397476698 | TUBB3 | c.1090T>C (p.Ser364Pro) n.4511T>C c.874T>C (p.Ser292Pro) c.277+1963T>C (n.277+1963T>C) c.*1175T>C (n.*1175T>C) c.2131T>C (p.Ser711Pro) | |
| 16 | g.89935541T>G | CA397476699 | TUBB3 | c.1090T>G (p.Ser364Ala) n.4511T>G c.874T>G (p.Ser292Ala) c.277+1963T>G (n.277+1963T>G) c.*1175T>G (n.*1175T>G) c.2131T>G (p.Ser711Ala) | |
| 16 | g.89935542C>A | CA397476700 | TUBB3 | c.1091C>A (p.Ser364Tyr) n.4512C>A c.875C>A (p.Ser292Tyr) c.277+1964C>A (n.277+1964C>A) c.*1176C>A (n.*1176C>A) c.2132C>A (p.Ser711Tyr) | |
| 16 | g.89935542C>G | CA397476701 | TUBB3 | c.1091C>G (p.Ser364Cys) n.4512C>G c.875C>G (p.Ser292Cys) c.277+1964C>G (n.277+1964C>G) c.*1176C>G (n.*1176C>G) c.2132C>G (p.Ser711Cys) | |
| 16 | g.89935542C>T | CA397476702 | TUBB3 | c.1091C>T (p.Ser364Phe) n.4512C>T c.875C>T (p.Ser292Phe) c.277+1964C>T (n.277+1964C>T) c.*1176C>T (n.*1176C>T) c.2132C>T (p.Ser711Phe) | ClinVar dbSNP gnomAD v4 |
| 16 | g.89935543C>A | CA497381562 | TUBB3 | c.1092C>A (p.Ser364=) n.4513C>A c.876C>A (p.Ser292=) c.277+1965C>A (n.277+1965C>A) c.*1177C>A (n.*1177C>A) c.2133C>A (p.Ser711=) | |
| 16 | g.89935543C>G | CA497381564 | TUBB3 | c.1092C>G (p.Ser364=) n.4513C>G c.876C>G (p.Ser292=) c.277+1965C>G (n.277+1965C>G) c.*1177C>G (n.*1177C>G) c.2133C>G (p.Ser711=) | |
| 16 | g.89935543C>T | CA497381566 | TUBB3 | c.1092C>T (p.Ser364=) n.4513C>T c.876C>T (p.Ser292=) c.277+1965C>T (n.277+1965C>T) c.*1177C>T (n.*1177C>T) c.2133C>T (p.Ser711=) | gnomAD v4 |
| 16 | g.89935544T>A | CA397476703 | TUBB3 | c.1093T>A (p.Ser365Thr) n.4514T>A c.877T>A (p.Ser293Thr) c.277+1966T>A (n.277+1966T>A) c.*1178T>A (n.*1178T>A) c.2134T>A (p.Ser712Thr) | dbSNP |
| 16 | g.89935544T>C | CA397476704 | TUBB3 | c.1093T>C (p.Ser365Pro) n.4514T>C c.877T>C (p.Ser293Pro) c.277+1966T>C (n.277+1966T>C) c.*1178T>C (n.*1178T>C) c.2134T>C (p.Ser712Pro) | |
| 16 | g.89935544T>G | CA397476705 | TUBB3 | c.1093T>G (p.Ser365Ala) n.4514T>G c.877T>G (p.Ser293Ala) c.277+1966T>G (n.277+1966T>G) c.*1178T>G (n.*1178T>G) c.2134T>G (p.Ser712Ala) | |
| 16 | g.89935545C>A | CA397476706 | TUBB3 | c.1094C>A (p.Ser365Tyr) n.4515C>A c.878C>A (p.Ser293Tyr) c.277+1967C>A (n.277+1967C>A) c.*1179C>A (n.*1179C>A) c.2135C>A (p.Ser712Tyr) | |
| 16 | g.89935545C>G | CA397476708 | TUBB3 | c.1094C>G (p.Ser365Cys) n.4515C>G c.878C>G (p.Ser293Cys) c.277+1967C>G (n.277+1967C>G) c.*1179C>G (n.*1179C>G) c.2135C>G (p.Ser712Cys) | |
| 16 | g.89935545C>T | CA397476707 | TUBB3 | c.1094C>T (p.Ser365Phe) n.4515C>T c.878C>T (p.Ser293Phe) c.277+1967C>T (n.277+1967C>T) c.*1179C>T (n.*1179C>T) c.2135C>T (p.Ser712Phe) | |
| 16 | g.89935546C>A | CA497381567 | TUBB3 | c.1095C>A (p.Ser365=) n.4516C>A c.879C>A (p.Ser293=) c.277+1968C>A (n.277+1968C>A) c.*1180C>A (n.*1180C>A) c.2136C>A (p.Ser712=) | |
| 16 | g.89935546C= | CA2242020556 | TUBB3 | c.1095C= (p.Ser365=) n.4516C= c.879C= (p.Ser293=) c.277+1968C= (n.277+1968C=) c.*1180C= (n.*1180C=) c.2136C= (p.Ser712=) | |
| 16 | g.89935546C>G | CA497381569 | TUBB3 | c.1095C>G (p.Ser365=) n.4516C>G c.879C>G (p.Ser293=) c.277+1968C>G (n.277+1968C>G) c.*1180C>G (n.*1180C>G) c.2136C>G (p.Ser712=) | |
| 16 | g.89935546C>T | CA497381570 | TUBB3 | c.1095C>T (p.Ser365=) n.4516C>T c.879C>T (p.Ser293=) c.277+1968C>T (n.277+1968C>T) c.*1180C>T (n.*1180C>T) c.2136C>T (p.Ser712=) | dbSNP gnomAD v4 |
| 16 | g.89935547A>C | CA397476709 | TUBB3 | c.1096A>C (p.Thr366Pro) n.4517A>C c.880A>C (p.Thr294Pro) c.277+1969A>C (n.277+1969A>C) c.*1181A>C (n.*1181A>C) c.2137A>C (p.Thr713Pro) | |
| 16 | g.89935547A>G | CA397476710 | TUBB3 | c.1096A>G (p.Thr366Ala) n.4517A>G c.880A>G (p.Thr294Ala) c.277+1969A>G (n.277+1969A>G) c.*1181A>G (n.*1181A>G) c.2137A>G (p.Thr713Ala) |