ClinVar Miner

List of variants in gene TUBGCP6 reported as benign by Invitae

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Gene type:
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Total variants: 88
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HGVS dbSNP gnomAD frequency
NM_020461.4(TUBGCP6):c.4315+20T>C rs6537642 0.96249
NM_020461.4(TUBGCP6):c.1700T>C (p.Leu567Ser) rs4838865 0.81410
NM_020461.4(TUBGCP6):c.4129A>G (p.Thr1377Ala) rs11703226 0.45122
NM_020461.4(TUBGCP6):c.24C>T (p.Phe8=) rs5771270 0.31375
NM_020461.4(TUBGCP6):c.4090A>T (p.Ser1364Cys) rs5771107 0.12667
NM_020461.4(TUBGCP6):c.4821+20G>A rs11912397 0.11469
NM_020461.4(TUBGCP6):c.5287C>T (p.Arg1763Trp) rs35381394 0.07476
NM_020461.4(TUBGCP6):c.1264T>C (p.Leu422=) rs6010211 0.05847
NM_020461.4(TUBGCP6):c.3441C>T (p.Asn1147=) rs73893142 0.05796
NM_020461.4(TUBGCP6):c.4734C>T (p.Ser1578=) rs34104775 0.04951
NM_020461.4(TUBGCP6):c.10A>G (p.Ile4Val) rs61736756 0.04335
NM_020461.4(TUBGCP6):c.2651C>T (p.Ala884Val) rs34455105 0.04155
NM_020461.4(TUBGCP6):c.4512C>T (p.Val1504=) rs17013240 0.03254
NM_020461.4(TUBGCP6):c.3190G>A (p.Gly1064Arg) rs149231425 0.02089
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.311T>C (p.Leu104Pro) rs8137873 0.01669
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.905+13C>G rs17248329 0.00933
NM_020461.4(TUBGCP6):c.3307C>T (p.Arg1103Trp) rs61739385 0.00849
NM_020461.4(TUBGCP6):c.3694G>A (p.Val1232Met) rs17248287 0.00755
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.4185G>T (p.Gln1395His) rs115418729 0.00350
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.2065+12C>T rs200568170 0.00138
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.1452G>A (p.Pro484=) rs114942206 0.00107
NM_020461.4(TUBGCP6):c.4347C>T (p.Pro1449=) rs188946019 0.00097
NM_020461.4(TUBGCP6):c.1291-6C>T rs201449189 0.00091
NM_020461.4(TUBGCP6):c.4479C>T (p.Ala1493=) rs150925794 0.00086
NM_020461.4(TUBGCP6):c.2574G>C (p.Trp858Cys) rs147989796 0.00084
NM_020461.4(TUBGCP6):c.2155-20A>G rs113835879 0.00076
NM_020461.4(TUBGCP6):c.3000G>T (p.Arg1000=) rs148461181 0.00066
NM_020461.4(TUBGCP6):c.2270+12C>T rs187563075 0.00058
NM_020461.4(TUBGCP6):c.5052C>T (p.Ile1684=) rs139368772 0.00048
NM_020461.4(TUBGCP6):c.2490G>C (p.Thr830=) rs146870875 0.00041
NM_020461.4(TUBGCP6):c.4955-13T>C rs376079883 0.00031
NM_020461.4(TUBGCP6):c.2484+20C>A rs200649141 0.00026
NM_020461.4(TUBGCP6):c.1044G>A (p.Lys348=) rs548131980 0.00023
NM_020461.4(TUBGCP6):c.1492-16C>G rs201446399 0.00023
NM_020461.4(TUBGCP6):c.5050A>G (p.Ile1684Val) rs146532216 0.00022
NM_020461.4(TUBGCP6):c.4221G>A (p.Ser1407=) rs142261025 0.00019
NM_020461.4(TUBGCP6):c.3459C>T (p.Pro1153=) rs200315229 0.00018
NM_020461.4(TUBGCP6):c.5113G>A (p.Asp1705Asn) rs202244591 0.00016
NM_020461.4(TUBGCP6):c.4168-13G>C rs369835169 0.00014
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.3447G>A (p.Ser1149=) rs181687065 0.00012
NM_020461.4(TUBGCP6):c.1413-6G>A rs373051985 0.00011
NM_020461.4(TUBGCP6):c.4584C>T (p.Asp1528=) rs757971501 0.00010
NM_020461.4(TUBGCP6):c.1413-9_1413-8del rs3841004 0.00009
NM_020461.4(TUBGCP6):c.2046G>A (p.Arg682=) rs140814808 0.00009
NM_020461.4(TUBGCP6):c.4875C>T (p.Ser1625=) rs373718907 0.00008
NM_020461.4(TUBGCP6):c.4002G>A (p.Ser1334=) rs551910403 0.00007
NM_020461.4(TUBGCP6):c.1962C>T (p.Ser654=) rs567031410 0.00006
NM_020461.4(TUBGCP6):c.3822G>A (p.Pro1274=) rs377666583 0.00006
NM_020461.4(TUBGCP6):c.5178C>T (p.Leu1726=) rs779558085 0.00006
NM_020461.4(TUBGCP6):c.5369-13C>T rs202182732 0.00005
NM_020461.4(TUBGCP6):c.2361G>A (p.Leu787=) rs541224216 0.00001
NM_020461.4(TUBGCP6):c.1700_1701inv (p.Leu567Ser)
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.4182C>T (p.Ala1394=) rs565771303
NM_020461.4(TUBGCP6):c.4227G>A (p.Ala1409=) rs200451987
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
NM_020461.4(TUBGCP6):c.4861= (p.Val1621=)
NM_020461.4(TUBGCP6):c.4861G>C (p.Val1621Leu) rs4838864
NM_020461.4(TUBGCP6):c.5169-8dup rs774240720
NM_020461.4(TUBGCP6):c.906-7dup

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