ClinVar Miner

List of variants in gene DOCK2 reported as uncertain significance by Ambry Genetics

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Gene type:
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Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_004946.3(DOCK2):c.2656G>A (p.Val886Ile) rs199862297 0.00025
NM_004946.3(DOCK2):c.1546T>C (p.Ser516Pro) rs201439364 0.00021
NM_004946.3(DOCK2):c.3140T>G (p.Phe1047Cys) rs145444170 0.00019
NM_004946.3(DOCK2):c.1486G>A (p.Ala496Thr) rs371391395 0.00016
NM_004946.3(DOCK2):c.2635G>A (p.Val879Ile) rs150884555 0.00014
NM_004946.3(DOCK2):c.2858C>T (p.Ser953Phe) rs35395501 0.00011
NM_004946.3(DOCK2):c.5377G>A (p.Gly1793Ser) rs146061014 0.00011
NM_004946.3(DOCK2):c.1023T>G (p.Asp341Glu) rs368378335 0.00009
NM_004946.3(DOCK2):c.1390A>G (p.Ile464Val) rs372498181 0.00009
NM_004946.3(DOCK2):c.4078G>A (p.Val1360Met) rs137922056 0.00008
NM_004946.3(DOCK2):c.5294C>T (p.Ala1765Val) rs141274816 0.00007
NM_004946.3(DOCK2):c.286T>C (p.Trp96Arg) rs370949354 0.00006
NM_004946.3(DOCK2):c.4459A>G (p.Met1487Val) rs750831425 0.00006
NM_004946.3(DOCK2):c.1597A>G (p.Lys533Glu) rs375363462 0.00005
NM_004946.3(DOCK2):c.3337G>A (p.Asp1113Asn) rs557824061 0.00005
NM_004946.3(DOCK2):c.5153C>T (p.Ser1718Leu) rs760040908 0.00005
NM_004946.3(DOCK2):c.134A>G (p.Tyr45Cys) rs150182906 0.00004
NM_004946.3(DOCK2):c.2315G>A (p.Arg772Gln) rs1232157605 0.00004
NM_004946.3(DOCK2):c.3190C>T (p.Arg1064Trp) rs772417044 0.00004
NM_004946.3(DOCK2):c.3599G>A (p.Arg1200His) rs373428643 0.00004
NM_004946.3(DOCK2):c.5267A>G (p.Gln1756Arg) rs779208637 0.00004
NM_004946.3(DOCK2):c.1349T>C (p.Met450Thr) rs759775916 0.00003
NM_004946.3(DOCK2):c.2435C>T (p.Ala812Val) rs775851597 0.00002
NM_004946.3(DOCK2):c.1986G>T (p.Glu662Asp) rs368933125 0.00001
NM_004946.3(DOCK2):c.2545A>G (p.Lys849Glu) rs773584607 0.00001
NM_004946.3(DOCK2):c.4163T>C (p.Met1388Thr) rs765831486 0.00001
NM_004946.3(DOCK2):c.4357G>A (p.Val1453Ile) rs749664205 0.00001
NM_004946.3(DOCK2):c.4769G>A (p.Arg1590Lys) rs747184048 0.00001
NM_004946.3(DOCK2):c.527A>G (p.Asp176Gly) rs753893848 0.00001
NM_004946.3(DOCK2):c.790C>T (p.Arg264Trp) rs764798982 0.00001
NM_004946.3(DOCK2):c.1060A>G (p.Thr354Ala)
NM_004946.3(DOCK2):c.107G>A (p.Arg36Gln)
NM_004946.3(DOCK2):c.119C>T (p.Thr40Met)
NM_004946.3(DOCK2):c.1468A>T (p.Met490Leu)
NM_004946.3(DOCK2):c.1651G>A (p.Val551Ile)
NM_004946.3(DOCK2):c.1784G>A (p.Ser595Asn)
NM_004946.3(DOCK2):c.2053G>A (p.Ala685Thr)
NM_004946.3(DOCK2):c.2170T>A (p.Ser724Thr)
NM_004946.3(DOCK2):c.2242G>A (p.Val748Ile)
NM_004946.3(DOCK2):c.2857T>A (p.Ser953Thr)
NM_004946.3(DOCK2):c.3056C>G (p.Thr1019Arg) rs368028175
NM_004946.3(DOCK2):c.3056C>T (p.Thr1019Met) rs368028175
NM_004946.3(DOCK2):c.3092A>T (p.His1031Leu)
NM_004946.3(DOCK2):c.367G>A (p.Asp123Asn)
NM_004946.3(DOCK2):c.3833A>G (p.Glu1278Gly)
NM_004946.3(DOCK2):c.4126A>T (p.Met1376Leu) rs768935540
NM_004946.3(DOCK2):c.4193T>C (p.Val1398Ala)
NM_004946.3(DOCK2):c.4273C>G (p.Pro1425Ala)
NM_004946.3(DOCK2):c.4418A>G (p.Tyr1473Cys)
NM_004946.3(DOCK2):c.4525A>C (p.Ile1509Leu)
NM_004946.3(DOCK2):c.454A>G (p.Ile152Val)
NM_004946.3(DOCK2):c.4879G>T (p.Asp1627Tyr) rs368481515
NM_004946.3(DOCK2):c.4960G>A (p.Asp1654Asn)
NM_004946.3(DOCK2):c.4985C>T (p.Thr1662Ile)
NM_004946.3(DOCK2):c.5002C>G (p.Leu1668Val)
NM_004946.3(DOCK2):c.5011G>A (p.Ala1671Thr)
NM_004946.3(DOCK2):c.5207C>T (p.Ser1736Leu)
NM_004946.3(DOCK2):c.5294C>A (p.Ala1765Glu)
NM_004946.3(DOCK2):c.5302G>A (p.Val1768Met)
NM_004946.3(DOCK2):c.604A>G (p.Met202Val)
NM_004946.3(DOCK2):c.650C>T (p.Ser217Leu)

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