ClinVar Miner

List of variants in gene DOCK7 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 97
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HGVS dbSNP gnomAD frequency
NM_001367561.1(DOCK7):c.885+201A>C rs41290148 0.02991
NM_001367561.1(DOCK7):c.5361+178T>C rs55744543 0.02203
NM_001367561.1(DOCK7):c.1801-823A>G rs58799727 0.01256
NM_001367561.1(DOCK7):c.5635-47G>A rs79655355 0.01233
NM_001367561.1(DOCK7):c.2471T>C (p.Ile824Thr) rs35400360 0.01182
NM_001367561.1(DOCK7):c.4283-117A>G rs115936118 0.01172
NM_001367561.1(DOCK7):c.1460A>G (p.Lys487Arg) rs72913293 0.01118
NM_001367561.1(DOCK7):c.2767-120T>A rs114368431 0.01051
NM_001367561.1(DOCK7):c.3045+89C>A rs116423924 0.00883
NM_001367561.1(DOCK7):c.4611+208C>A rs6669089 0.00870
NM_001367561.1(DOCK7):c.5361+64A>G rs116020848 0.00801
NM_001367561.1(DOCK7):c.2011-98G>A rs55838487 0.00711
NM_001367561.1(DOCK7):c.2112+137G>A rs116371127 0.00675
NM_001367561.1(DOCK7):c.818+177C>T rs74078656 0.00656
NM_001367561.1(DOCK7):c.389+94T>G rs150386658 0.00653
NM_001367561.1(DOCK7):c.5362-69T>C rs114326497 0.00653
NM_001367561.1(DOCK7):c.39-125T>C rs147822272 0.00652
NM_001367561.1(DOCK7):c.390-210A>G rs141677458 0.00651
NM_001367561.1(DOCK7):c.3300+25G>A rs141549705 0.00642
NM_001367561.1(DOCK7):c.3046-291A>G rs182267560 0.00626
NM_001367561.1(DOCK7):c.6106-312C>T rs141314882 0.00626
NM_001367561.1(DOCK7):c.4612-246T>C rs114878881 0.00604
NM_001367561.1(DOCK7):c.4696G>A (p.Gly1566Ser) rs147103646 0.00601
NM_001367561.1(DOCK7):c.4765-206C>T rs186930664 0.00584
NM_001367561.1(DOCK7):c.4380-216C>T rs187259556 0.00583
NM_001367561.1(DOCK7):c.4380-217A>T rs190803571 0.00583
NM_001367561.1(DOCK7):c.1392A>G (p.Pro464=) rs116172511 0.00571
NM_001367561.1(DOCK7):c.1683-143C>T rs148137031 0.00553
NM_001367561.1(DOCK7):c.6106-163A>G rs116569821 0.00526
NM_001367561.1(DOCK7):c.1801-1290C>G rs140835259 0.00403
NM_001367561.1(DOCK7):c.1682+90T>G rs151075830 0.00401
NM_001367561.1(DOCK7):c.1800+1552A>T rs145204658 0.00395
NM_001367561.1(DOCK7):c.1872-181C>T rs181465052 0.00394
NM_001367561.1(DOCK7):c.1519+88dup rs563667621 0.00390
NM_001367561.1(DOCK7):c.4764+191del rs367867953 0.00390
NM_001367561.1(DOCK7):c.4379+175G>A rs144952434 0.00379
NM_001367561.1(DOCK7):c.2767-191A>T rs556992175 0.00333
NM_001367561.1(DOCK7):c.*96G>T rs114747052 0.00326
NM_001367561.1(DOCK7):c.1047C>T (p.Val349=) rs139793443 0.00290
NM_001367561.1(DOCK7):c.2700C>T (p.Ser900=) rs35648144 0.00154
NM_001367561.1(DOCK7):c.125A>G (p.Asn42Ser) rs143701798 0.00133
NM_001367561.1(DOCK7):c.3935C>T (p.Thr1312Met) rs59558623 0.00125
NM_001367561.1(DOCK7):c.4668G>A (p.Arg1556=) rs115353638 0.00107
NM_001367561.1(DOCK7):c.480T>C (p.Ser160=) rs142535471 0.00083
NM_001367561.1(DOCK7):c.4368G>A (p.Glu1456=) rs149367921 0.00036
NM_001367561.1(DOCK7):c.6018G>A (p.Glu2006=) rs143414077 0.00029
NM_001367561.1(DOCK7):c.156C>T (p.Thr52=) rs147045113 0.00025
NM_001367561.1(DOCK7):c.4653T>C (p.Ala1551=) rs150922364 0.00021
NM_001367561.1(DOCK7):c.6045C>T (p.Pro2015=) rs202231787 0.00019
NM_001367561.1(DOCK7):c.3717C>G (p.Ala1239=) rs375372678 0.00016
NM_001367561.1(DOCK7):c.4491G>A (p.Thr1497=) rs373928701 0.00016
NM_001367561.1(DOCK7):c.5208A>T (p.Val1736=) rs144604663 0.00016
NM_001367561.1(DOCK7):c.4056A>G (p.Ser1352=) rs144949335 0.00011
NM_001367561.1(DOCK7):c.5463T>A (p.Leu1821=) rs201081054 0.00006
NM_001367561.1(DOCK7):c.2250C>T (p.His750=) rs201252647 0.00003
NM_001367561.1(DOCK7):c.72C>T (p.Ser24=) rs369563931 0.00003
NM_001367561.1(DOCK7):c.1182T>C (p.Tyr394=) rs768933704 0.00001
NM_001367561.1(DOCK7):c.1293G>T (p.Gly431=) rs777222905 0.00001
NM_001367561.1(DOCK7):c.258T>C (p.Asp86=) rs767000347 0.00001
NM_001367561.1(DOCK7):c.281G>A (p.Arg94Gln) rs570514826 0.00001
NM_001367561.1(DOCK7):c.5796C>T (p.Phe1932=) rs771762947 0.00001
NM_001367561.1(DOCK7):c.999C>T (p.Ile333=) rs758427747 0.00001
NM_001367561.1(DOCK7):c.*155C>T
NM_001367561.1(DOCK7):c.1283-14del rs541344421
NM_001367561.1(DOCK7):c.1283-9C>A rs1325493384
NM_001367561.1(DOCK7):c.1410A>C (p.Thr470=)
NM_001367561.1(DOCK7):c.171A>C (p.Pro57=)
NM_001367561.1(DOCK7):c.1801-1565T>C
NM_001367561.1(DOCK7):c.1872-9del rs199915737
NM_001367561.1(DOCK7):c.2010+123C>G rs181452771
NM_001367561.1(DOCK7):c.2597-133_2597-132del rs66892340
NM_001367561.1(DOCK7):c.2597-135_2597-132dup rs66892340
NM_001367561.1(DOCK7):c.2597-152_2597-151dup rs66892340
NM_001367561.1(DOCK7):c.2955T>C (p.Phe985=) rs1571471147
NM_001367561.1(DOCK7):c.3046-278del rs111463668
NM_001367561.1(DOCK7):c.3060G>A (p.Val1020=)
NM_001367561.1(DOCK7):c.3114A>G (p.Pro1038=)
NM_001367561.1(DOCK7):c.3471+304_3471+305del rs34404898
NM_001367561.1(DOCK7):c.3486T>G (p.Ser1162=)
NM_001367561.1(DOCK7):c.3936+275_3936+276dup rs34335688
NM_001367561.1(DOCK7):c.3937-113_3937-109del rs372559346
NM_001367561.1(DOCK7):c.3937-95_3937-94del rs143439247
NM_001367561.1(DOCK7):c.4095C>T (p.Leu1365=) rs1314563293
NM_001367561.1(DOCK7):c.4282+188_4282+190del rs61042514
NM_001367561.1(DOCK7):c.4282+190del rs61042514
NM_001367561.1(DOCK7):c.4380-205_4380-201del rs369440201
NM_001367561.1(DOCK7):c.4765-73dup rs200220657
NM_001367561.1(DOCK7):c.4923+252_4923+255del rs55649868
NM_001367561.1(DOCK7):c.5025-151C>G rs56120442
NM_001367561.1(DOCK7):c.5064G>A (p.Leu1688=) rs2149298969
NM_001367561.1(DOCK7):c.5362-316C>T rs186926212
NM_001367561.1(DOCK7):c.5493+231_5493+232dup rs57650980
NM_001367561.1(DOCK7):c.5772G>A (p.Glu1924=) rs1571222064
NM_001367561.1(DOCK7):c.5829C>T (p.Tyr1943=)
NM_001367561.1(DOCK7):c.6108G>A (p.Gly2036=)
NM_001367561.1(DOCK7):c.6381-6dup rs773882812
NM_001367561.1(DOCK7):c.819-58C>G rs17123735

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