ClinVar Miner

Variants in gene TUBGCP6 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 37
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_020461.4(TUBGCP6):c.3513G>A (p.Leu1171=) rs61745994 0.02068
NM_020461.4(TUBGCP6):c.3408C>T (p.His1136=) rs17013247 0.02018
NM_020461.4(TUBGCP6):c.4764C>T (p.Pro1588=) rs78122876 0.01126
NM_020461.4(TUBGCP6):c.4728C>T (p.His1576=) rs34562250 0.01049
NM_020461.4(TUBGCP6):c.681C>T (p.Asp227=) rs147321582 0.00981
NM_020461.4(TUBGCP6):c.3307C>T (p.Arg1103Trp) rs61739385 0.00849
NM_020461.4(TUBGCP6):c.5181G>A (p.Thr1727=) rs35231253 0.00736
NM_020461.4(TUBGCP6):c.4821+14C>T rs55985560 0.00692
NM_020461.4(TUBGCP6):c.3092G>C (p.Gly1031Ala) rs115728769 0.00455
NM_020461.4(TUBGCP6):c.1443T>C (p.Ala481=) rs141766585 0.00451
NM_020461.4(TUBGCP6):c.2066-11T>C rs113592725 0.00429
NM_020461.4(TUBGCP6):c.837C>T (p.Asp279=) rs34718948 0.00417
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.2487C>G (p.Val829=) rs139343360 0.00248
NM_020461.4(TUBGCP6):c.4929C>T (p.Asp1643=) rs147939592 0.00234
NM_020461.4(TUBGCP6):c.1612G>A (p.Asp538Asn) rs139934957 0.00230
NM_020461.4(TUBGCP6):c.5139C>T (p.His1713=) rs149152116 0.00206
NM_020461.4(TUBGCP6):c.3651T>C (p.His1217=) rs148914897 0.00154
NM_020461.4(TUBGCP6):c.4223C>T (p.Ala1408Val) rs142798996 0.00153
NM_020461.4(TUBGCP6):c.3496G>A (p.Asp1166Asn) rs3747943 0.00136
NM_020461.4(TUBGCP6):c.4398C>T (p.Ala1466=) rs142496306 0.00135
NM_020461.4(TUBGCP6):c.2991C>T (p.Ser997=) rs143388326 0.00134
NM_020461.4(TUBGCP6):c.1291-6C>T rs201449189 0.00091
NM_020461.4(TUBGCP6):c.2574G>C (p.Trp858Cys) rs147989796 0.00084
NM_020461.4(TUBGCP6):c.5052C>T (p.Ile1684=) rs139368772 0.00048
NM_020461.4(TUBGCP6):c.5113G>A (p.Asp1705Asn) rs202244591 0.00016
NM_020461.4(TUBGCP6):c.3240C>T (p.His1080=) rs145410588 0.00013
NM_020461.4(TUBGCP6):c.1611C>T (p.His537=) rs201235588 0.00012
NM_020461.4(TUBGCP6):c.4875C>T (p.Ser1625=) rs373718907 0.00008
NM_020461.4(TUBGCP6):c.2361G>A (p.Leu787=) rs541224216 0.00001
NM_020461.4(TUBGCP6):c.3189C>G (p.Val1063=) rs117613659
NM_020461.4(TUBGCP6):c.3732C>T (p.His1244=) rs140699312
NM_020461.4(TUBGCP6):c.42C>A (p.Ala14=) rs146878404
NM_020461.4(TUBGCP6):c.4317C>A (p.Ser1439=) rs79022493
NM_020461.4(TUBGCP6):c.4317C>T (p.Ser1439=) rs79022493
NM_020461.4(TUBGCP6):c.4326C>T (p.Pro1442=) rs76633938

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.