ClinVar Miner

List of variants in gene TUBB3 reported as uncertain significance for not provided

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Gene type:
ClinVar version:
Total variants: 104
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HGVS dbSNP gnomAD frequency
NM_006086.4(TUBB3):c.921C>T (p.His307=) rs147283850 0.00083
NM_006086.4(TUBB3):c.357G>A (p.Val119=) rs34174718 0.00040
NM_006086.4(TUBB3):c.507C>T (p.Val169=) rs373718068 0.00033
NM_006086.4(TUBB3):c.109G>A (p.Val37Met) rs372720472 0.00004
NM_006086.4(TUBB3):c.813C>T (p.Ala271=) rs776465410 0.00002
NM_006086.4(TUBB3):c.1147G>A (p.Glu383Lys) rs762254443 0.00001
NM_006086.4(TUBB3):c.1331C>T (p.Ser444Leu) rs587784504 0.00001
NM_006086.4(TUBB3):c.137G>A (p.Arg46Gln) rs1333706172 0.00001
NM_006086.4(TUBB3):c.210C>T (p.Pro70=) rs754683361 0.00001
NM_006086.4(TUBB3):c.606C>T (p.Ile202=) rs576180572 0.00001
NM_006086.4(TUBB3):c.1013G>A (p.Ser338Asn)
NM_006086.4(TUBB3):c.1057G>A (p.Val353Met) rs1597425155
NM_006086.4(TUBB3):c.1070C>T (p.Pro357Leu) rs2151093027
NM_006086.4(TUBB3):c.1075C>T (p.Arg359Cys)
NM_006086.4(TUBB3):c.107A>G (p.Tyr36Cys)
NM_006086.4(TUBB3):c.1091C>T (p.Ser364Phe) rs2151093047
NM_006086.4(TUBB3):c.1128G>T (p.Glu376Asp)
NM_006086.4(TUBB3):c.1139G>A (p.Arg380His) rs777149755
NM_006086.4(TUBB3):c.1156A>T (p.Thr386Ser) rs2030427563
NM_006086.4(TUBB3):c.1157C>T (p.Thr386Met)
NM_006086.4(TUBB3):c.115G>A (p.Asp39Asn)
NM_006086.4(TUBB3):c.1165T>G (p.Phe389Val) rs1131691959
NM_006086.4(TUBB3):c.1169G>C (p.Arg390Pro) rs886042295
NM_006086.4(TUBB3):c.1213G>C (p.Glu405Gln)
NM_006086.4(TUBB3):c.1226C>T (p.Thr409Ile)
NM_006086.4(TUBB3):c.1239C>G (p.Ser413Arg) rs2151093115
NM_006086.4(TUBB3):c.1261G>A (p.Glu421Lys) rs2151093126
NM_006086.4(TUBB3):c.1267C>T (p.Gln423Ter) rs2151093129
NM_006086.4(TUBB3):c.1271A>C (p.Gln424Pro)
NM_006086.4(TUBB3):c.1282G>A (p.Ala428Thr)
NM_006086.4(TUBB3):c.1286C>T (p.Thr429Met)
NM_006086.4(TUBB3):c.1291G>T (p.Glu431Ter)
NM_006086.4(TUBB3):c.1303G>A (p.Glu435Lys)
NM_006086.4(TUBB3):c.1307T>C (p.Met436Thr) rs758528369
NM_006086.4(TUBB3):c.1312G>C (p.Glu438Gln) rs11554952
NM_006086.4(TUBB3):c.1318G>C (p.Asp440His) rs781596774
NM_006086.4(TUBB3):c.1318G>T (p.Asp440Tyr)
NM_006086.4(TUBB3):c.1321G>A (p.Glu441Lys)
NM_006086.4(TUBB3):c.1334A>G (p.Glu445Gly)
NM_006086.4(TUBB3):c.1337C>T (p.Ala446Val) rs2151093168
NM_006086.4(TUBB3):c.136C>T (p.Arg46Trp) rs1555625363
NM_006086.4(TUBB3):c.156C>G (p.Asn52Lys)
NM_006086.4(TUBB3):c.157G>A (p.Glu53Lys)
NM_006086.4(TUBB3):c.166+6T>C
NM_006086.4(TUBB3):c.187G>A (p.Ala63Thr)
NM_006086.4(TUBB3):c.200A>T (p.Asp67Val)
NM_006086.4(TUBB3):c.205G>A (p.Glu69Lys)
NM_006086.4(TUBB3):c.205G>C (p.Glu69Gln)
NM_006086.4(TUBB3):c.221A>G (p.Asp74Gly) rs2030344761
NM_006086.4(TUBB3):c.271A>G (p.Ile91Val)
NM_006086.4(TUBB3):c.277+6T>C
NM_006086.4(TUBB3):c.318C>G (p.Tyr106Ter) rs1220586790
NM_006086.4(TUBB3):c.320C>T (p.Thr107Met) rs2030395720
NM_006086.4(TUBB3):c.328G>A (p.Ala110Thr)
NM_006086.4(TUBB3):c.358G>T (p.Val120Leu)
NM_006086.4(TUBB3):c.377A>C (p.Asn126Thr)
NM_006086.4(TUBB3):c.386G>A (p.Cys129Tyr) rs2151092738
NM_006086.4(TUBB3):c.418G>T (p.Gly140Trp)
NM_006086.4(TUBB3):c.436G>A (p.Gly146Ser) rs2151092771
NM_006086.4(TUBB3):c.439A>C (p.Met147Leu)
NM_006086.4(TUBB3):c.446C>T (p.Thr149Met) rs2030399551
NM_006086.4(TUBB3):c.466C>T (p.Arg156Cys)
NM_006086.4(TUBB3):c.467G>A (p.Arg156His)
NM_006086.4(TUBB3):c.474G>C (p.Glu158Asp)
NM_006086.4(TUBB3):c.492G>T (p.Met164Ile)
NM_006086.4(TUBB3):c.505G>A (p.Val169Ile)
NM_006086.4(TUBB3):c.515C>T (p.Ser172Leu) rs2151092797
NM_006086.4(TUBB3):c.517C>T (p.Pro173Ser)
NM_006086.4(TUBB3):c.523G>T (p.Val175Leu)
NM_006086.4(TUBB3):c.557C>T (p.Thr186Met)
NM_006086.4(TUBB3):c.578T>C (p.Val193Ala) rs2151092822
NM_006086.4(TUBB3):c.58-3C>A
NM_006086.4(TUBB3):c.580G>A (p.Glu194Lys)
NM_006086.4(TUBB3):c.638G>A (p.Arg213His)
NM_006086.4(TUBB3):c.670G>A (p.Asp224Asn)
NM_006086.4(TUBB3):c.677A>G (p.Asn226Ser) rs1221483017
NM_006086.4(TUBB3):c.71T>C (p.Ile24Thr) rs1567763964
NM_006086.4(TUBB3):c.730G>T (p.Gly244Cys) rs2030410834
NM_006086.4(TUBB3):c.752G>A (p.Arg251His) rs2151092893
NM_006086.4(TUBB3):c.756G>A (p.Lys252=)
NM_006086.4(TUBB3):c.766A>T (p.Asn256Tyr) rs1064796443
NM_006086.4(TUBB3):c.772G>T (p.Val258Leu)
NM_006086.4(TUBB3):c.801G>A (p.Met267Ile)
NM_006086.4(TUBB3):c.802C>T (p.Pro268Ser)
NM_006086.4(TUBB3):c.805G>A (p.Gly269Ser) rs2151092918
NM_006086.4(TUBB3):c.815C>A (p.Pro272His) rs2151092925
NM_006086.4(TUBB3):c.833G>A (p.Ser278Asn)
NM_006086.4(TUBB3):c.836A>G (p.Gln279Arg) rs2030416493
NM_006086.4(TUBB3):c.83A>G (p.His28Arg)
NM_006086.4(TUBB3):c.845G>A (p.Arg282Gln) rs1064795231
NM_006086.4(TUBB3):c.854C>T (p.Thr285Ile)
NM_006086.4(TUBB3):c.860C>T (p.Pro287Leu) rs2151092939
NM_006086.4(TUBB3):c.895A>G (p.Met299Val)
NM_006086.4(TUBB3):c.897G>T (p.Met299Ile)
NM_006086.4(TUBB3):c.922G>A (p.Gly308Ser)
NM_006086.4(TUBB3):c.925C>T (p.Arg309Cys) rs2151092961
NM_006086.4(TUBB3):c.935C>T (p.Thr312Met) rs777771368
NM_006086.4(TUBB3):c.946G>A (p.Val316Met) rs797046077
NM_006086.4(TUBB3):c.952C>T (p.Arg318Trp) rs183017345
NM_006086.4(TUBB3):c.959G>T (p.Arg320Leu)
NM_006086.4(TUBB3):c.963G>A (p.Met321Ile) rs2151092980
NM_006086.4(TUBB3):c.970A>C (p.Lys324Gln)
NM_006086.4(TUBB3):c.982G>A (p.Glu328Lys) rs1057518686
NM_006086.4(TUBB3):c.985C>G (p.Gln329Glu)

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