ClinVar Miner

List of variants in gene TUBB3 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 94
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HGVS dbSNP gnomAD frequency
NM_006086.4(TUBB3):c.702C>T (p.Ser234=) rs147245174 0.00879
NM_006086.4(TUBB3):c.1215G>A (p.Glu405=) rs141064323 0.00809
NM_001197181.2(TUBB3):c.-160+1028C>T rs558683187 0.00347
NM_006086.4(TUBB3):c.278-404C>T rs578076761 0.00177
NM_006086.4(TUBB3):c.435C>T (p.Ser145=) rs146421795 0.00153
NM_006086.4(TUBB3):c.666C>T (p.Tyr222=) rs61743676 0.00117
NM_006086.4(TUBB3):c.921C>T (p.His307=) rs147283850 0.00083
NM_006086.4(TUBB3):c.277+155G>A rs551983164 0.00072
NM_006086.4(TUBB3):c.357G>A (p.Val119=) rs34174718 0.00040
NM_006086.4(TUBB3):c.507C>T (p.Val169=) rs373718068 0.00031
NM_006086.4(TUBB3):c.1197G>A (p.Thr399=) rs371418131 0.00021
NM_006086.4(TUBB3):c.278-16T>C rs200799871 0.00015
NM_006086.4(TUBB3):c.381C>T (p.Cys127=) rs145375049 0.00011
NM_006086.4(TUBB3):c.855C>T (p.Thr285=) rs201682024 0.00011
NM_006086.4(TUBB3):c.1056C>T (p.Ala352=) rs201308325 0.00009
NM_006086.4(TUBB3):c.534G>A (p.Thr178=) rs143029958 0.00009
NM_006086.4(TUBB3):c.90C>T (p.Ile30=) rs369355135 0.00009
NM_006086.4(TUBB3):c.1158G>A (p.Thr386=) rs773849361 0.00008
NM_006086.4(TUBB3):c.1233C>T (p.Ala411=) rs780355761 0.00007
NM_006086.4(TUBB3):c.741C>T (p.Asn247=) rs138498822 0.00006
NM_006086.4(TUBB3):c.225T>C (p.Ser75=) rs199612798 0.00005
NM_006086.4(TUBB3):c.278-19C>T rs746314997 0.00005
NM_006086.4(TUBB3):c.414G>A (p.Ser138=) rs113548504 0.00005
NM_006086.4(TUBB3):c.552C>T (p.Asn184=) rs546465562 0.00005
NM_006086.4(TUBB3):c.588G>A (p.Thr196=) rs374448137 0.00005
NM_006086.4(TUBB3):c.903C>T (p.Ala301=) rs143913140 0.00005
NM_006086.4(TUBB3):c.909C>T (p.Cys303=) rs372795851 0.00005
NM_006086.4(TUBB3):c.1200C>T (p.Gly400=) rs144689076 0.00004
NM_006086.4(TUBB3):c.558G>A (p.Thr186=) rs558112305 0.00004
NM_006086.4(TUBB3):c.58-19del rs755935820 0.00004
NM_006086.4(TUBB3):c.882C>T (p.Phe294=) rs753163862 0.00004
NM_006086.4(TUBB3):c.1116G>A (p.Thr372=) rs566062002 0.00003
NM_006086.4(TUBB3):c.114C>T (p.Gly38=) rs149711112 0.00003
NM_006086.4(TUBB3):c.1326G>A (p.Glu442=) rs144036692 0.00003
NM_006086.4(TUBB3):c.816C>G (p.Pro272=) rs748070053 0.00003
NM_006086.4(TUBB3):c.861C>T (p.Pro287=) rs759943633 0.00003
NM_006086.4(TUBB3):c.915G>A (p.Pro305=) rs758099244 0.00003
NM_006086.4(TUBB3):c.975G>A (p.Glu325=) rs113763477 0.00003
NM_006086.4(TUBB3):c.99C>T (p.Ser33=) rs760662331 0.00003
NM_006086.4(TUBB3):c.1077C>T (p.Arg359=) rs777734748 0.00002
NM_006086.4(TUBB3):c.657G>A (p.Thr219=) rs778395569 0.00002
NM_006086.4(TUBB3):c.813C>T (p.Ala271=) rs776465410 0.00002
NM_006086.4(TUBB3):c.936G>A (p.Thr312=) rs375770255 0.00002
NM_006086.4(TUBB3):c.1071G>A (p.Pro357=) rs754560439 0.00001
NM_006086.4(TUBB3):c.1146C>T (p.Ser382=) rs11554953 0.00001
NM_006086.4(TUBB3):c.1206C>T (p.Gly402=) rs757192357 0.00001
NM_006086.4(TUBB3):c.1227C>T (p.Thr409=) rs758588994 0.00001
NM_006086.4(TUBB3):c.1260C>T (p.Ser420=) rs759051850 0.00001
NM_006086.4(TUBB3):c.1332G>A (p.Ser444=) rs559133379 0.00001
NM_006086.4(TUBB3):c.1336G>A (p.Ala446Thr) rs369454228 0.00001
NM_006086.4(TUBB3):c.138G>A (p.Arg46=) rs750682582 0.00001
NM_006086.4(TUBB3):c.167-19A>C rs2544625554 0.00001
NM_006086.4(TUBB3):c.210C>T (p.Pro70=) rs754683361 0.00001
NM_006086.4(TUBB3):c.278-5T>C rs368806076 0.00001
NM_006086.4(TUBB3):c.291C>T (p.Ala97=) rs1230372819 0.00001
NM_006086.4(TUBB3):c.345G>A (p.Ser115=) rs201439214 0.00001
NM_006086.4(TUBB3):c.387C>T (p.Cys129=) rs746393721 0.00001
NM_006086.4(TUBB3):c.501C>T (p.Phe167=) rs757357850 0.00001
NM_006086.4(TUBB3):c.609C>T (p.Asp203=) rs376993247 0.00001
NM_006086.4(TUBB3):c.750G>A (p.Leu250=) rs778434867 0.00001
NM_006086.4(TUBB3):c.759G>A (p.Leu253=) rs1329478812 0.00001
NM_006086.4(TUBB3):c.762C>T (p.Ala254=) rs758044135 0.00001
NM_006086.4(TUBB3):c.1001A>G (p.Gln334Arg) rs2544627964
NM_006086.4(TUBB3):c.1080C>T (p.Gly360=) rs140825096
NM_006086.4(TUBB3):c.1104C>T (p.Ile368=)
NM_006086.4(TUBB3):c.120G>T (p.Ser40=) rs765264294
NM_006086.4(TUBB3):c.1257G>T (p.Val419=) rs770275598
NM_006086.4(TUBB3):c.1329G>A (p.Glu443=) rs749705105
NM_006086.4(TUBB3):c.1352G>A (p.Ter451=)
NM_006086.4(TUBB3):c.159G>A (p.Glu53=)
NM_006086.4(TUBB3):c.166+8C>A rs1340728450
NM_006086.4(TUBB3):c.167-20G>A rs764702998
NM_006086.4(TUBB3):c.167-21C>G rs72813449
NM_006086.4(TUBB3):c.189C>G (p.Ala63=) rs146730216
NM_006086.4(TUBB3):c.198G>A (p.Val66=) rs751066850
NM_006086.4(TUBB3):c.246A>T (p.Gly82=)
NM_006086.4(TUBB3):c.278-175C>G rs75635769
NM_006086.4(TUBB3):c.342T>C (p.Asp114=) rs1597424632
NM_006086.4(TUBB3):c.348C>G (p.Val116=) rs1443330509
NM_006086.4(TUBB3):c.567C>A (p.Ile189=)
NM_006086.4(TUBB3):c.58-13A>T
NM_006086.4(TUBB3):c.58-17T>C rs2544624608
NM_006086.4(TUBB3):c.58-20C>T rs747564957
NM_006086.4(TUBB3):c.684G>C (p.Leu228=) rs776744775
NM_006086.4(TUBB3):c.717C>G (p.Ser239=) rs2151092874
NM_006086.4(TUBB3):c.72C>T (p.Ile24=) rs2030316527
NM_006086.4(TUBB3):c.783G>A (p.Pro261=) rs746788686
NM_006086.4(TUBB3):c.783G>C (p.Pro261=) rs746788686
NM_006086.4(TUBB3):c.804C>T (p.Pro268=) rs368243859
NM_006086.4(TUBB3):c.873G>A (p.Gln291=)
NM_006086.4(TUBB3):c.926G>A (p.Arg309His) rs780983495
NM_006086.4(TUBB3):c.960C>T (p.Arg320=) rs1597425097
NM_006086.4(TUBB3):c.972G>A (p.Lys324=) rs767365635
NM_006086.4(TUBB3):c.993G>C (p.Leu331=) rs61743716

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