ClinVar Miner

List of variants in gene TUBGCP6 reported by Genetic Services Laboratory, University of Chicago

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Total variants: 57
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HGVS dbSNP gnomAD frequency
NM_020461.4(TUBGCP6):c.5181G>A (p.Thr1727=) rs35231253 0.00736
NM_020461.4(TUBGCP6):c.3396T>C (p.Asn1132=) rs879175668 0.00551
NM_020461.4(TUBGCP6):c.2021C>T (p.Ala674Val) rs35446002 0.00357
NM_020461.4(TUBGCP6):c.1118C>T (p.Pro373Leu) rs34273213 0.00348
NM_020461.4(TUBGCP6):c.3382A>C (p.Arg1128=) rs1266725037 0.00264
NM_020461.4(TUBGCP6):c.4929C>T (p.Asp1643=) rs147939592 0.00234
NM_020461.4(TUBGCP6):c.5139C>T (p.His1713=) rs149152116 0.00206
NM_020461.4(TUBGCP6):c.89G>A (p.Arg30Gln) rs148626062 0.00200
NM_020461.4(TUBGCP6):c.3651T>C (p.His1217=) rs148914897 0.00154
NM_020461.4(TUBGCP6):c.3490G>A (p.Val1164Met) rs9628306 0.00153
NM_020461.4(TUBGCP6):c.4223C>T (p.Ala1408Val) rs142798996 0.00153
NM_020461.4(TUBGCP6):c.2991C>T (p.Ser997=) rs143388326 0.00134
NM_020461.4(TUBGCP6):c.1452G>A (p.Pro484=) rs114942206 0.00107
NM_020461.4(TUBGCP6):c.3300T>C (p.Thr1100=) rs778386409 0.00086
NM_020461.4(TUBGCP6):c.2574G>C (p.Trp858Cys) rs147989796 0.00084
NM_020461.4(TUBGCP6):c.1193C>T (p.Ser398Leu) rs142435821 0.00062
NM_020461.4(TUBGCP6):c.3193G>A (p.Glu1065Lys) rs143759693 0.00062
NM_020461.4(TUBGCP6):c.1026G>A (p.Pro342=) rs141805017 0.00055
NM_020461.4(TUBGCP6):c.1539C>T (p.Cys513=) rs149982006 0.00051
NM_020461.4(TUBGCP6):c.2724G>A (p.Pro908=) rs140491142 0.00050
NM_020461.4(TUBGCP6):c.3898C>T (p.His1300Tyr) rs148601529 0.00048
NM_020461.4(TUBGCP6):c.5052C>T (p.Ile1684=) rs139368772 0.00048
NM_020461.4(TUBGCP6):c.161C>G (p.Thr54Ser) rs139974572 0.00041
NM_020461.4(TUBGCP6):c.5013C>T (p.His1671=) rs146637907 0.00029
NM_020461.4(TUBGCP6):c.2043C>T (p.Ser681=) rs142854750 0.00020
NM_020461.4(TUBGCP6):c.5285C>T (p.Pro1762Leu) rs201721812 0.00020
NM_020461.4(TUBGCP6):c.655G>T (p.Val219Leu) rs137934849 0.00019
NM_020461.4(TUBGCP6):c.4026C>T (p.Ser1342=) rs763335019 0.00018
NM_020461.4(TUBGCP6):c.1119G>A (p.Pro373=) rs144698883 0.00014
NM_020461.4(TUBGCP6):c.2489C>T (p.Thr830Met) rs758201280 0.00014
NM_020461.4(TUBGCP6):c.245T>G (p.Leu82Arg) rs200360214 0.00008
NM_020461.4(TUBGCP6):c.2065+9C>T rs781746721 0.00006
NM_020461.4(TUBGCP6):c.3822G>A (p.Pro1274=) rs377666583 0.00006
NM_020461.4(TUBGCP6):c.4051G>C (p.Ala1351Pro) rs200701438 0.00006
NM_020461.4(TUBGCP6):c.4520T>A (p.Phe1507Tyr) rs146136859 0.00006
NM_020461.4(TUBGCP6):c.4954+10C>T rs200824422 0.00005
NM_020461.4(TUBGCP6):c.945G>A (p.Ala315=) rs144685624 0.00005
NM_020461.4(TUBGCP6):c.1304G>A (p.Gly435Asp) rs368378157 0.00004
NM_020461.4(TUBGCP6):c.895C>T (p.Arg299Ter) rs192919234 0.00004
NM_020461.4(TUBGCP6):c.2066-6A>G rs368765755 0.00003
NM_020461.4(TUBGCP6):c.3451G>A (p.Val1151Met) rs750851968 0.00002
NM_020461.4(TUBGCP6):c.5161G>A (p.Val1721Ile) rs377506638 0.00002
NM_020461.4(TUBGCP6):c.1511A>G (p.Tyr504Cys) rs745507206 0.00001
NM_020461.4(TUBGCP6):c.1529T>G (p.Leu510Arg) rs777796155 0.00001
NM_020461.4(TUBGCP6):c.1716C>T (p.Gly572=) rs1163635070 0.00001
NM_020461.4(TUBGCP6):c.2356C>T (p.Arg786Ter) rs772174079 0.00001
NM_020461.4(TUBGCP6):c.4587C>T (p.Gly1529=) rs554921650 0.00001
NM_020461.4(TUBGCP6):c.4876G>A (p.Gly1626Ser) rs201575861 0.00001
NM_020461.4(TUBGCP6):c.1700_1701inv (p.Leu567Ser)
NM_020461.4(TUBGCP6):c.2198G>C (p.Ser733Thr) rs1422096763
NM_020461.4(TUBGCP6):c.2727C>T (p.Ser909=) rs375889859
NM_020461.4(TUBGCP6):c.2893C>T (p.Pro965Ser) rs797046079
NM_020461.4(TUBGCP6):c.3090A>C (p.Ser1030=)
NM_020461.4(TUBGCP6):c.3288T>A (p.Asp1096Glu) rs6010209
NM_020461.4(TUBGCP6):c.3291G>T (p.Val1097=) rs1555907480
NM_020461.4(TUBGCP6):c.3532A>T (p.Met1178Leu) rs1215314321
NM_020461.4(TUBGCP6):c.42C>A (p.Ala14=) rs146878404

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