ClinVar Miner

List of variants in gene DOCK7 reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 71
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HGVS dbSNP gnomAD frequency
NM_001367561.1(DOCK7):c.2605G>A (p.Gly869Ser) rs201823761 0.00069
NM_001367561.1(DOCK7):c.2908A>G (p.Ser970Gly) rs199681303 0.00026
NM_001367561.1(DOCK7):c.2932C>T (p.Arg978Cys) rs750049987 0.00021
NM_001367561.1(DOCK7):c.1585C>T (p.Leu529Phe) rs142744313 0.00019
NM_001367561.1(DOCK7):c.3781+4C>G rs372305581 0.00019
NM_001367561.1(DOCK7):c.1292G>C (p.Gly431Ala) rs201785444 0.00018
NM_001367561.1(DOCK7):c.160G>A (p.Ala54Thr) rs150216310 0.00017
NM_001367561.1(DOCK7):c.5486T>A (p.Val1829Asp) rs375887190 0.00015
NM_001367561.1(DOCK7):c.2797A>G (p.Thr933Ala) rs780996734 0.00013
NM_001367561.1(DOCK7):c.2020A>G (p.Met674Val) rs115733789 0.00011
NM_001367561.1(DOCK7):c.6254C>T (p.Pro2085Leu) rs753509954 0.00011
NM_001367561.1(DOCK7):c.2371C>A (p.Leu791Ile) rs146210506 0.00009
NM_001367561.1(DOCK7):c.2612G>A (p.Gly871Glu) rs142531051 0.00007
NM_001367561.1(DOCK7):c.5477G>A (p.Ser1826Asn) rs182780540 0.00007
NM_001367561.1(DOCK7):c.145G>A (p.Val49Met) rs374725632 0.00006
NM_001367561.1(DOCK7):c.4019A>G (p.Asp1340Gly) rs143210310 0.00006
NM_001367561.1(DOCK7):c.3250G>A (p.Val1084Ile) rs758986234 0.00005
NM_001367561.1(DOCK7):c.3646G>A (p.Val1216Ile) rs755704781 0.00005
NM_001367561.1(DOCK7):c.6407G>A (p.Arg2136His) rs201452223 0.00004
NM_001367561.1(DOCK7):c.5693C>G (p.Pro1898Arg) rs747709595 0.00003
NM_001367561.1(DOCK7):c.1979A>G (p.Asn660Ser) rs1313541793 0.00002
NM_001367561.1(DOCK7):c.2188A>G (p.Ile730Val) rs747262593 0.00002
NM_001367561.1(DOCK7):c.2927C>T (p.Thr976Met) rs780945471 0.00002
NM_001367561.1(DOCK7):c.4852C>T (p.Arg1618Cys) rs766160359 0.00002
NM_001367561.1(DOCK7):c.1142A>G (p.Lys381Arg) rs148287864 0.00001
NM_001367561.1(DOCK7):c.2203C>G (p.Pro735Ala) rs773479192 0.00001
NM_001367561.1(DOCK7):c.230G>A (p.Arg77Gln) rs376620846 0.00001
NM_001367561.1(DOCK7):c.2735A>T (p.Asp912Val) rs780210369 0.00001
NM_001367561.1(DOCK7):c.3031T>C (p.Phe1011Leu) rs770299891 0.00001
NM_001367561.1(DOCK7):c.3065A>T (p.His1022Leu) rs1333564606 0.00001
NM_001367561.1(DOCK7):c.3098G>A (p.Arg1033Lys) rs1413099334 0.00001
NM_001367561.1(DOCK7):c.3335G>T (p.Ser1112Ile) rs762113697 0.00001
NM_001367561.1(DOCK7):c.3503A>G (p.Gln1168Arg) rs201976376 0.00001
NM_001367561.1(DOCK7):c.3626A>G (p.His1209Arg) rs776656811 0.00001
NM_001367561.1(DOCK7):c.3686A>T (p.Tyr1229Phe) rs752478136 0.00001
NM_001367561.1(DOCK7):c.5219A>G (p.Asn1740Ser) rs764324822 0.00001
NM_001367561.1(DOCK7):c.5233G>A (p.Val1745Ile) rs1646505300 0.00001
NM_001367561.1(DOCK7):c.5942A>G (p.Asn1981Ser) rs145796299 0.00001
NM_001367561.1(DOCK7):c.748C>T (p.Arg250Trp) rs373543179 0.00001
NM_001367561.1(DOCK7):c.109C>T (p.Leu37Phe)
NM_001367561.1(DOCK7):c.1254T>A (p.Asp418Glu) rs1022211823
NM_001367561.1(DOCK7):c.1349CAA[1] (p.Thr451del) rs750703394
NM_001367561.1(DOCK7):c.1351A>T (p.Thr451Ser) rs145829350
NM_001367561.1(DOCK7):c.1610G>A (p.Ser537Asn) rs1327760633
NM_001367561.1(DOCK7):c.1690C>T (p.Leu564Phe) rs1647565613
NM_001367561.1(DOCK7):c.1890A>G (p.Glu630=) rs1647025196
NM_001367561.1(DOCK7):c.1909C>T (p.Pro637Ser)
NM_001367561.1(DOCK7):c.1963T>A (p.Cys655Ser)
NM_001367561.1(DOCK7):c.2107C>A (p.Pro703Thr)
NM_001367561.1(DOCK7):c.2365C>T (p.Leu789Phe) rs1646235697
NM_001367561.1(DOCK7):c.2527A>T (p.Ser843Cys)
NM_001367561.1(DOCK7):c.2531_2532delinsGC (p.Leu844Arg) rs2149432744
NM_001367561.1(DOCK7):c.2554G>A (p.Val852Ile) rs2525074715
NM_001367561.1(DOCK7):c.256G>A (p.Asp86Asn) rs867320510
NM_001367561.1(DOCK7):c.2755A>G (p.Ile919Val)
NM_001367561.1(DOCK7):c.2774A>G (p.Asp925Gly)
NM_001367561.1(DOCK7):c.2941A>G (p.Thr981Ala)
NM_001367561.1(DOCK7):c.302C>T (p.Ser101Leu) rs2149694292
NM_001367561.1(DOCK7):c.3172T>G (p.Ser1058Ala) rs1430899085
NM_001367561.1(DOCK7):c.3290G>T (p.Cys1097Phe) rs1480512837
NM_001367561.1(DOCK7):c.3577G>A (p.Glu1193Lys) rs548706843
NM_001367561.1(DOCK7):c.3676G>A (p.Asp1226Asn) rs1645108056
NM_001367561.1(DOCK7):c.3871A>C (p.Met1291Leu)
NM_001367561.1(DOCK7):c.5384A>C (p.Asn1795Thr) rs2523962572
NM_001367561.1(DOCK7):c.5560G>T (p.Asp1854Tyr) rs1191345154
NM_001367561.1(DOCK7):c.5684A>C (p.Asp1895Ala) rs1474922484
NM_001367561.1(DOCK7):c.5855G>T (p.Arg1952Leu) rs149407043
NM_001367561.1(DOCK7):c.691C>T (p.Arg231Cys) rs1254316274
NM_001367561.1(DOCK7):c.856G>A (p.Ala286Thr)
NM_001367561.1(DOCK7):c.964A>G (p.Ile322Val) rs2149634956
NM_001367561.1(DOCK7):c.997A>G (p.Ile333Val)

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