ClinVar Miner

Variants in gene DOCK6 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: 51
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HGVS dbSNP gnomAD frequency
NM_020812.4(DOCK6):c.4895C>T (p.Ala1632Val) rs117328686 0.02223
NM_020812.4(DOCK6):c.2956-5C>T rs3810309 0.01873
NM_020812.4(DOCK6):c.4258G>C (p.Val1420Leu) rs8108071 0.01108
NM_020812.4(DOCK6):c.1992C>T (p.His664=) rs116286520 0.01079
NM_020812.4(DOCK6):c.441G>C (p.Lys147Asn) rs34545822 0.00959
NM_020812.4(DOCK6):c.3913C>T (p.Arg1305Cys) rs112911897 0.00801
NM_020812.4(DOCK6):c.1833-8T>A rs7252321 0.00708
NM_020812.4(DOCK6):c.5700G>A (p.Thr1900=) rs142270471 0.00651
NM_020812.4(DOCK6):c.4933G>A (p.Val1645Ile) rs34853494 0.00645
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.2160+5G>A rs150276162 0.00405
NM_020812.4(DOCK6):c.4344G>A (p.Pro1448=) rs200307398 0.00331
NM_020812.4(DOCK6):c.4197C>T (p.Ile1399=) rs35583018 0.00306
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.3752G>A (p.Arg1251Gln) rs200390354 0.00245
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.4479C>T (p.Phe1493=) rs146048288 0.00173
NM_020812.4(DOCK6):c.5939+6C>T rs200393834 0.00149
NM_020812.4(DOCK6):c.1993G>A (p.Gly665Arg) rs17001264 0.00148
NM_020812.4(DOCK6):c.810C>T (p.Phe270=) rs372611420 0.00140
NM_020812.4(DOCK6):c.4869G>A (p.Ala1623=) rs187249194 0.00107
NM_020812.4(DOCK6):c.2104G>A (p.Gly702Ser) rs199838752 0.00102
NM_020812.4(DOCK6):c.1608C>T (p.Pro536=) rs114902682 0.00096
NM_020812.4(DOCK6):c.2883C>T (p.Pro961=) rs370648857 0.00073
NM_020812.4(DOCK6):c.4548G>A (p.Thr1516=) rs377755210 0.00064
NM_020812.4(DOCK6):c.729C>G (p.Ala243=) rs35674395 0.00061
NM_020812.4(DOCK6):c.4107-13T>A rs369430502 0.00046
NM_020812.4(DOCK6):c.5088+8C>G rs147181483 0.00042
NM_020812.4(DOCK6):c.1643+5G>A rs117014874 0.00037
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.2506G>A (p.Val836Ile) rs200935357 0.00011
NM_020812.4(DOCK6):c.2103C>T (p.Asp701=) rs372208548 0.00006
NM_020812.4(DOCK6):c.4253A>G (p.Lys1418Arg) rs530689577 0.00006
NM_020812.4(DOCK6):c.4446C>T (p.Ser1482=) rs529459880 0.00006
NM_020812.4(DOCK6):c.12C>G (p.Ser4=) rs560244093 0.00005
NM_020812.4(DOCK6):c.258G>T (p.Leu86=) rs563605363 0.00003
NM_020812.4(DOCK6):c.*67G>A
NM_020812.4(DOCK6):c.2140G>A (p.Val714Met)
NM_020812.4(DOCK6):c.2346G>A (p.Lys782=)
NM_020812.4(DOCK6):c.2550G>C (p.Pro850=) rs73506659
NM_020812.4(DOCK6):c.2772C>G (p.Arg924=) rs201482446
NM_020812.4(DOCK6):c.5469G>A (p.Thr1823=)
NM_020812.4(DOCK6):c.5832+4C>T rs572880984
NM_020812.4(DOCK6):c.906G>C (p.Ser302=) rs79202547
NM_020812.4(DOCK6):c.945C>T (p.His315=)

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