ClinVar Miner

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

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Total variants: 27
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HGVS dbSNP
NM_020461.4(TUBGCP6):c.1026G>A (p.Pro342=) rs141805017
NM_020461.4(TUBGCP6):c.1193C>T (p.Ser398Leu) rs142435821
NM_020461.4(TUBGCP6):c.1304G>A (p.Gly435Asp) rs368378157
NM_020461.4(TUBGCP6):c.1452G>A (p.Pro484=) rs114942206
NM_020461.4(TUBGCP6):c.1511A>G (p.Tyr504Cys) rs745507206
NM_020461.4(TUBGCP6):c.1529T>G (p.Leu510Arg) rs777796155
NM_020461.4(TUBGCP6):c.1539C>T (p.Cys513=) rs149982006
NM_020461.4(TUBGCP6):c.161C>G (p.Thr54Ser) rs139974572
NM_020461.4(TUBGCP6):c.2065+9C>T rs781746721
NM_020461.4(TUBGCP6):c.2066-6A>G rs368765755
NM_020461.4(TUBGCP6):c.2198G>C (p.Ser733Thr) rs1422096763
NM_020461.4(TUBGCP6):c.245T>G (p.Leu82Arg) rs200360214
NM_020461.4(TUBGCP6):c.2489C>T (p.Thr830Met) rs758201280
NM_020461.4(TUBGCP6):c.2893C>T (p.Pro965Ser) rs797046079
NM_020461.4(TUBGCP6):c.3193G>A (p.Glu1065Lys) rs143759693
NM_020461.4(TUBGCP6):c.3288T>A (p.Asp1096Glu) rs6010209
NM_020461.4(TUBGCP6):c.3382A>C (p.Arg1128=) rs1266725037
NM_020461.4(TUBGCP6):c.3490G>A (p.Val1164Met) rs9628306
NM_020461.4(TUBGCP6):c.3532A>T (p.Met1178Leu) rs1215314321
NM_020461.4(TUBGCP6):c.3898C>T (p.His1300Tyr) rs148601529
NM_020461.4(TUBGCP6):c.4051G>C (p.Ala1351Pro) rs200701438
NM_020461.4(TUBGCP6):c.4587C>T (p.Gly1529=) rs554921650
NM_020461.4(TUBGCP6):c.4954+10C>T rs200824422
NM_020461.4(TUBGCP6):c.5161G>A (p.Val1721Ile) rs377506638
NM_020461.4(TUBGCP6):c.5285C>T (p.Pro1762Leu) rs201721812
NM_020461.4(TUBGCP6):c.655G>T (p.Val219Leu) rs137934849
NM_020461.4(TUBGCP6):c.89G>A (p.Arg30Gln) rs148626062

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