ClinVar Miner

List of variants in gene DOCK6 reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_020812.4(DOCK6):c.3913C>T (p.Arg1305Cys) rs112911897 0.00801
NM_020812.4(DOCK6):c.434G>A (p.Arg145Gln) rs140883567 0.00446
NM_020812.4(DOCK6):c.4205C>T (p.Thr1402Met) rs147554257 0.00411
NM_020812.4(DOCK6):c.4344G>A (p.Pro1448=) rs200307398 0.00331
NM_020812.4(DOCK6):c.1289G>A (p.Arg430His) rs143655255 0.00330
NM_020812.4(DOCK6):c.4197C>T (p.Ile1399=) rs35583018 0.00306
NM_020812.4(DOCK6):c.650G>A (p.Arg217Gln) rs35464191 0.00292
NM_020812.4(DOCK6):c.1959C>T (p.Pro653=) rs200269584 0.00273
NM_020812.4(DOCK6):c.4899G>A (p.Leu1633=) rs72985308 0.00255
NM_020812.4(DOCK6):c.5229C>A (p.Gly1743=) rs56243833 0.00246
NM_020812.4(DOCK6):c.1068G>C (p.Glu356Asp) rs73925150 0.00235
NM_020812.4(DOCK6):c.3526T>C (p.Leu1176=) rs200883815 0.00235
NM_020812.4(DOCK6):c.630G>A (p.Ala210=) rs114634227 0.00214
NM_020812.4(DOCK6):c.5976T>A (p.Ile1992=) rs200181665 0.00201
NM_020812.4(DOCK6):c.3517C>T (p.Arg1173Trp) rs145081732 0.00180
NM_020812.4(DOCK6):c.4862T>C (p.Val1621Ala) rs201738818 0.00166
NM_020812.4(DOCK6):c.5939+6C>T rs200393834 0.00149
NM_020812.4(DOCK6):c.133G>A (p.Val45Ile) rs183060698 0.00141
NM_020812.4(DOCK6):c.5640C>T (p.His1880=) rs200959822 0.00109
NM_020812.4(DOCK6):c.2104G>A (p.Gly702Ser) rs199838752 0.00102
NM_020812.4(DOCK6):c.5582G>A (p.Arg1861His) rs115035890 0.00093
NM_020812.4(DOCK6):c.2766C>T (p.Ala922=) rs372509134 0.00056
NM_020812.4(DOCK6):c.518G>A (p.Arg173Gln) rs373956807 0.00053
NM_020812.4(DOCK6):c.760C>T (p.Arg254Cys) rs144085374 0.00032
NM_020812.4(DOCK6):c.2790C>T (p.His930=) rs199846066 0.00028
NM_020812.4(DOCK6):c.744C>T (p.Ser248=) rs369049785 0.00024
NM_020812.4(DOCK6):c.3456C>T (p.Tyr1152=) rs761619087 0.00020
NM_020812.4(DOCK6):c.4068C>T (p.Ser1356=) rs370567682 0.00020
NM_020812.4(DOCK6):c.2373G>C (p.Pro791=) rs373234884 0.00019
NM_020812.4(DOCK6):c.3873C>T (p.Cys1291=) rs200843111 0.00019
NM_020812.4(DOCK6):c.1761+6T>C rs200659753 0.00016
NM_020812.4(DOCK6):c.3029G>A (p.Arg1010Gln) rs375754955 0.00012
NM_020812.4(DOCK6):c.3054G>A (p.Arg1018=) rs369415057 0.00011
NM_020812.4(DOCK6):c.5106G>A (p.Ala1702=) rs375692275 0.00007
NM_020812.4(DOCK6):c.2103C>T (p.Asp701=) rs372208548 0.00006
NM_020812.4(DOCK6):c.4096C>T (p.Arg1366Cys) rs200809206 0.00005
NM_020812.4(DOCK6):c.2973G>A (p.Glu991=) rs775738941 0.00004
NM_020812.4(DOCK6):c.4226G>A (p.Arg1409Gln) rs370312234 0.00004
NM_020812.4(DOCK6):c.258G>T (p.Leu86=) rs563605363 0.00003
NM_020812.4(DOCK6):c.4350G>C (p.Leu1450=) rs763073235 0.00002
NM_020812.4(DOCK6):c.5271C>T (p.Tyr1757=) rs757959680 0.00002
NM_020812.4(DOCK6):c.3518G>A (p.Arg1173Gln) rs776711205 0.00001
NM_020812.4(DOCK6):c.4786C>T (p.Arg1596Trp) rs764872626 0.00001
NM_020812.4(DOCK6):c.*67G>A
NM_020812.4(DOCK6):c.1011C>T (p.Phe337=)
NM_020812.4(DOCK6):c.12C>T (p.Ser4=)
NM_020812.4(DOCK6):c.1517A>C (p.Asn506Thr)
NM_020812.4(DOCK6):c.2140G>A (p.Val714Met)
NM_020812.4(DOCK6):c.2511C>T (p.His837=)
NM_020812.4(DOCK6):c.2676T>C (p.Pro892=)
NM_020812.4(DOCK6):c.2772C>T (p.Arg924=)
NM_020812.4(DOCK6):c.2965C>G (p.Leu989Val)
NM_020812.4(DOCK6):c.3163G>A (p.Val1055Met) rs202209921
NM_020812.4(DOCK6):c.3789C>T (p.Asn1263=)
NM_020812.4(DOCK6):c.3831A>G (p.Thr1277=)
NM_020812.4(DOCK6):c.4398C>G (p.Leu1466=)
NM_020812.4(DOCK6):c.4916A>C (p.His1639Pro)
NM_020812.4(DOCK6):c.492C>T (p.Ser164=)
NM_020812.4(DOCK6):c.5076C>T (p.Gly1692=)
NM_020812.4(DOCK6):c.5181C>T (p.His1727=)
NM_020812.4(DOCK6):c.5238C>A (p.Arg1746=)
NM_020812.4(DOCK6):c.5419C>T (p.Pro1807Ser)
NM_020812.4(DOCK6):c.5424G>A (p.Val1808=)
NM_020812.4(DOCK6):c.5469G>A (p.Thr1823=)
NM_020812.4(DOCK6):c.906G>C (p.Ser302=) rs79202547
NM_020812.4(DOCK6):c.945C>T (p.His315=)

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