ClinVar Miner

List of variants in gene TUBB3 reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 44
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HGVS dbSNP gnomAD frequency
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.137G>A (p.Arg46Gln) rs1333706172 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.1091C>T (p.Ser364Phe) rs2151093047
NM_006086.4(TUBB3):c.1139G>A (p.Arg380His) rs777149755
NM_006086.4(TUBB3):c.1165T>G (p.Phe389Val) rs1131691959
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.1291G>T (p.Glu431Ter)
NM_006086.4(TUBB3):c.1307T>C (p.Met436Thr) rs758528369
NM_006086.4(TUBB3):c.1337C>T (p.Ala446Val) rs2151093168
NM_006086.4(TUBB3):c.166+6T>C
NM_006086.4(TUBB3):c.200A>T (p.Asp67Val)
NM_006086.4(TUBB3):c.205G>A (p.Glu69Lys)
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.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.439A>C (p.Met147Leu)
NM_006086.4(TUBB3):c.446C>T (p.Thr149Met) rs2030399551
NM_006086.4(TUBB3):c.492G>T (p.Met164Ile)
NM_006086.4(TUBB3):c.515C>T (p.Ser172Leu) rs2151092797
NM_006086.4(TUBB3):c.557C>T (p.Thr186Met)
NM_006086.4(TUBB3):c.578T>C (p.Val193Ala) rs2151092822
NM_006086.4(TUBB3):c.638G>A (p.Arg213His)
NM_006086.4(TUBB3):c.670G>A (p.Asp224Asn)
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.766A>T (p.Asn256Tyr) rs1064796443
NM_006086.4(TUBB3):c.801G>A (p.Met267Ile)
NM_006086.4(TUBB3):c.805G>A (p.Gly269Ser) rs2151092918
NM_006086.4(TUBB3):c.854C>T (p.Thr285Ile)
NM_006086.4(TUBB3):c.895A>G (p.Met299Val)
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.952C>T (p.Arg318Trp) rs183017345
NM_006086.4(TUBB3):c.963G>A (p.Met321Ile) rs2151092980
NM_006086.4(TUBB3):c.970A>C (p.Lys324Gln)

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