ClinVar Miner

List of variants in gene TUBGCP6 reported as benign

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Gene type:
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Total variants: 80
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HGVS dbSNP
GRCh37/hg19 22q13.33(chr22:50674924-50676786)x1
GRCh37/hg19 22q13.33(chr22:50674924-50676855)x1
NM_020461.4(TUBGCP6):c.10A>G (p.Ile4Val)
NM_020461.4(TUBGCP6):c.1118C>T (p.Pro373Leu) rs34273213
NM_020461.4(TUBGCP6):c.1264T>C (p.Leu422=)
NM_020461.4(TUBGCP6):c.1291-6C>T rs201449189
NM_020461.4(TUBGCP6):c.1413-6G>A
NM_020461.4(TUBGCP6):c.1413-9_1413-8del
NM_020461.4(TUBGCP6):c.1443T>C (p.Ala481=) rs141766585
NM_020461.4(TUBGCP6):c.1452G>A (p.Pro484=) rs114942206
NM_020461.4(TUBGCP6):c.1492-16C>G
NM_020461.4(TUBGCP6):c.1611C>T (p.His537=) rs201235588
NM_020461.4(TUBGCP6):c.1612G>A (p.Asp538Asn) rs139934957
NM_020461.4(TUBGCP6):c.1700T>C (p.Leu567Ser) rs4838865
NM_020461.4(TUBGCP6):c.1700_1701inv (p.Leu567Ser)
NM_020461.4(TUBGCP6):c.1962C>T (p.Ser654=)
NM_020461.4(TUBGCP6):c.2021C>T (p.Ala674Val) rs35446002
NM_020461.4(TUBGCP6):c.2046G>A (p.Arg682=)
NM_020461.4(TUBGCP6):c.2065+12C>T
NM_020461.4(TUBGCP6):c.2066-11T>C
NM_020461.4(TUBGCP6):c.2270+12C>T
NM_020461.4(TUBGCP6):c.2484+20C>A
NM_020461.4(TUBGCP6):c.2487C>G (p.Val829=) rs139343360
NM_020461.4(TUBGCP6):c.2490G>C (p.Thr830=) rs146870875
NM_020461.4(TUBGCP6):c.24C>T (p.Phe8=) rs5771270
NM_020461.4(TUBGCP6):c.2574G>C (p.Trp858Cys) rs147989796
NM_020461.4(TUBGCP6):c.2991C>T (p.Ser997=) rs143388326
NM_020461.4(TUBGCP6):c.3000G>T (p.Arg1000=)
NM_020461.4(TUBGCP6):c.3092G>C (p.Gly1031Ala) rs115728769
NM_020461.4(TUBGCP6):c.311T>C (p.Leu104Pro) rs8137873
NM_020461.4(TUBGCP6):c.3189C>G (p.Val1063=) rs117613659
NM_020461.4(TUBGCP6):c.3190G>A (p.Gly1064Arg)
NM_020461.4(TUBGCP6):c.3240C>T (p.His1080=) rs145410588
NM_020461.4(TUBGCP6):c.3307C>T (p.Arg1103Trp) rs61739385
NM_020461.4(TUBGCP6):c.3408C>T (p.His1136=)
NM_020461.4(TUBGCP6):c.3441C>T (p.Asn1147=)
NM_020461.4(TUBGCP6):c.3459C>T (p.Pro1153=) rs200315229
NM_020461.4(TUBGCP6):c.3496G>A (p.Asp1166Asn) rs3747943
NM_020461.4(TUBGCP6):c.3513G>A (p.Leu1171=)
NM_020461.4(TUBGCP6):c.3651T>C (p.His1217=) rs148914897
NM_020461.4(TUBGCP6):c.3694G>A (p.Val1232Met)
NM_020461.4(TUBGCP6):c.3732C>T (p.His1244=) rs140699312
NM_020461.4(TUBGCP6):c.3822G>A (p.Pro1274=)
NM_020461.4(TUBGCP6):c.4002G>A (p.Ser1334=)
NM_020461.4(TUBGCP6):c.4090A>T (p.Ser1364Cys)
NM_020461.4(TUBGCP6):c.4129A>G (p.Thr1377Ala) rs11703226
NM_020461.4(TUBGCP6):c.4182C>T (p.Ala1394=)
NM_020461.4(TUBGCP6):c.4185G>T (p.Gln1395His) rs115418729
NM_020461.4(TUBGCP6):c.4221G>A (p.Ser1407=) rs142261025
NM_020461.4(TUBGCP6):c.4223C>T (p.Ala1408Val) rs142798996
NM_020461.4(TUBGCP6):c.4227G>A (p.Ala1409=)
NM_020461.4(TUBGCP6):c.42C>A (p.Ala14=) rs146878404
NM_020461.4(TUBGCP6):c.4315+20T>C rs6537642
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.4347C>T (p.Pro1449=) rs188946019
NM_020461.4(TUBGCP6):c.4398C>T (p.Ala1466=) rs142496306
NM_020461.4(TUBGCP6):c.4479C>T (p.Ala1493=) rs150925794
NM_020461.4(TUBGCP6):c.4512C>T (p.Val1504=) rs17013240
NM_020461.4(TUBGCP6):c.4584C>T (p.Asp1528=)
NM_020461.4(TUBGCP6):c.4728C>T (p.His1576=) rs34562250
NM_020461.4(TUBGCP6):c.4734C>T (p.Ser1578=)
NM_020461.4(TUBGCP6):c.4764C>T (p.Pro1588=) rs78122876
NM_020461.4(TUBGCP6):c.4821+14C>T rs55985560
NM_020461.4(TUBGCP6):c.4821+20G>A
NM_020461.4(TUBGCP6):c.4861= (p.Val1621=)
NM_020461.4(TUBGCP6):c.4861G>C (p.Val1621Leu)
NM_020461.4(TUBGCP6):c.4875C>T (p.Ser1625=) rs373718907
NM_020461.4(TUBGCP6):c.4929C>T (p.Asp1643=) rs147939592
NM_020461.4(TUBGCP6):c.5050A>G (p.Ile1684Val) rs146532216
NM_020461.4(TUBGCP6):c.5052C>T (p.Ile1684=) rs139368772
NM_020461.4(TUBGCP6):c.5139C>T (p.His1713=) rs149152116
NM_020461.4(TUBGCP6):c.5169-8dup
NM_020461.4(TUBGCP6):c.5178C>T (p.Leu1726=) rs779558085
NM_020461.4(TUBGCP6):c.5181G>A (p.Thr1727=) rs35231253
NM_020461.4(TUBGCP6):c.5287C>T (p.Arg1763Trp) rs35381394
NM_020461.4(TUBGCP6):c.681C>T (p.Asp227=)
NM_020461.4(TUBGCP6):c.837C>T (p.Asp279=) rs34718948
NM_020461.4(TUBGCP6):c.905+13C>G

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