ClinVar Miner

List of variants reported as uncertain significance for DOCK2 deficiency

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 128
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HGVS dbSNP
NM_004946.3(DOCK2):c.1023T>G (p.Asp341Glu)
NM_004946.3(DOCK2):c.103G>T (p.Val35Leu)
NM_004946.3(DOCK2):c.1057G>C (p.Val353Leu) rs1581055881
NM_004946.3(DOCK2):c.1082A>C (p.His361Pro)
NM_004946.3(DOCK2):c.1169T>C (p.Ile390Thr)
NM_004946.3(DOCK2):c.1216G>A (p.Val406Met)
NM_004946.3(DOCK2):c.1288C>G (p.Leu430Val) rs370264550
NM_004946.3(DOCK2):c.1334A>G (p.Asn445Ser) rs371303142
NM_004946.3(DOCK2):c.1349T>C (p.Met450Thr) rs759775916
NM_004946.3(DOCK2):c.1390A>G (p.Ile464Val)
NM_004946.3(DOCK2):c.1396G>A (p.Val466Met)
NM_004946.3(DOCK2):c.1426T>C (p.Tyr476His) rs769211157
NM_004946.3(DOCK2):c.1427A>G (p.Tyr476Cys)
NM_004946.3(DOCK2):c.1429C>T (p.Arg477Cys)
NM_004946.3(DOCK2):c.1482+6_1482+8del
NM_004946.3(DOCK2):c.1486G>A (p.Ala496Thr) rs371391395
NM_004946.3(DOCK2):c.148A>C (p.Ile50Leu) rs200852440
NM_004946.3(DOCK2):c.1540C>T (p.Arg514Trp) rs1169435264
NM_004946.3(DOCK2):c.1597A>G (p.Lys533Glu) rs375363462
NM_004946.3(DOCK2):c.1606A>G (p.Lys536Glu) rs1581078478
NM_004946.3(DOCK2):c.1738G>A (p.Ala580Thr)
NM_004946.3(DOCK2):c.1742C>T (p.Thr581Met) rs140817788
NM_004946.3(DOCK2):c.1753A>C (p.Ser585Arg) rs1466532077
NM_004946.3(DOCK2):c.1756T>C (p.Ser586Pro) rs1265967996
NM_004946.3(DOCK2):c.1785C>G (p.Ser595Arg)
NM_004946.3(DOCK2):c.1843+6C>T rs374362264
NM_004946.3(DOCK2):c.1986G>T (p.Glu662Asp)
NM_004946.3(DOCK2):c.2042T>C (p.Ile681Thr)
NM_004946.3(DOCK2):c.2051T>A (p.Ile684Asn) rs1400969417
NM_004946.3(DOCK2):c.2175C>G (p.Ser725Arg) rs1561633059
NM_004946.3(DOCK2):c.2315G>A (p.Arg772Gln)
NM_004946.3(DOCK2):c.2342T>C (p.Met781Thr)
NM_004946.3(DOCK2):c.236A>G (p.Asn79Ser)
NM_004946.3(DOCK2):c.239T>G (p.Ile80Ser)
NM_004946.3(DOCK2):c.2435C>T (p.Ala812Val)
NM_004946.3(DOCK2):c.2447+4A>G rs1581150663
NM_004946.3(DOCK2):c.2479C>T (p.Pro827Ser) rs1581153476
NM_004946.3(DOCK2):c.2485G>T (p.Val829Leu)
NM_004946.3(DOCK2):c.2525T>C (p.Ile842Thr) rs148384873
NM_004946.3(DOCK2):c.2635G>A (p.Val879Ile)
NM_004946.3(DOCK2):c.2638C>A (p.Leu880Met) rs112062072
NM_004946.3(DOCK2):c.2656G>A (p.Val886Ile) rs199862297
NM_004946.3(DOCK2):c.2704-3C>T
NM_004946.3(DOCK2):c.2742G>C (p.Gln914His) rs761742890
NM_004946.3(DOCK2):c.2858C>T (p.Ser953Phe) rs35395501
NM_004946.3(DOCK2):c.2867T>C (p.Ile956Thr)
NM_004946.3(DOCK2):c.286T>C (p.Trp96Arg) rs370949354
NM_004946.3(DOCK2):c.2938A>G (p.Ile980Val)
NM_004946.3(DOCK2):c.2976G>A (p.Met992Ile)
NM_004946.3(DOCK2):c.301A>C (p.Ile101Leu)
NM_004946.3(DOCK2):c.3056C>G (p.Thr1019Arg)
NM_004946.3(DOCK2):c.3140T>G (p.Phe1047Cys) rs145444170
NM_004946.3(DOCK2):c.3148G>A (p.Ala1050Thr)
NM_004946.3(DOCK2):c.3190C>T (p.Arg1064Trp)
NM_004946.3(DOCK2):c.3233G>A (p.Gly1078Asp) rs1561883336
NM_004946.3(DOCK2):c.3236A>C (p.Gln1079Pro)
NM_004946.3(DOCK2):c.3293T>C (p.Ile1098Thr)
NM_004946.3(DOCK2):c.3310C>T (p.Arg1104Trp) rs780318765
NM_004946.3(DOCK2):c.3311G>A (p.Arg1104Gln)
NM_004946.3(DOCK2):c.3337G>A (p.Asp1113Asn) rs557824061
NM_004946.3(DOCK2):c.3366T>A (p.Ser1122Arg) rs200973349
NM_004946.3(DOCK2):c.338G>A (p.Arg113His) rs750421267
NM_004946.3(DOCK2):c.3484G>A (p.Ala1162Thr) rs1581543762
NM_004946.3(DOCK2):c.3496A>G (p.Thr1166Ala)
NM_004946.3(DOCK2):c.3547G>A (p.Glu1183Lys) rs1581543832
NM_004946.3(DOCK2):c.3568G>A (p.Gly1190Ser) rs777118797
NM_004946.3(DOCK2):c.360G>A (p.Met120Ile) rs752809346
NM_004946.3(DOCK2):c.3683G>A (p.Arg1228His) rs139600790
NM_004946.3(DOCK2):c.3794C>T (p.Thr1265Ile) rs768197840
NM_004946.3(DOCK2):c.3854T>C (p.Ile1285Thr) rs369071999
NM_004946.3(DOCK2):c.3925G>A (p.Glu1309Lys)
NM_004946.3(DOCK2):c.3986A>G (p.Tyr1329Cys) rs766635884
NM_004946.3(DOCK2):c.4018C>T (p.Pro1340Ser) rs752947346
NM_004946.3(DOCK2):c.4060T>A (p.Ser1354Thr) rs550928168
NM_004946.3(DOCK2):c.4091G>A (p.Arg1364His)
NM_004946.3(DOCK2):c.4126A>T (p.Met1376Leu)
NM_004946.3(DOCK2):c.4135A>T (p.Met1379Leu)
NM_004946.3(DOCK2):c.4147C>T (p.Pro1383Ser) rs938288633
NM_004946.3(DOCK2):c.4151A>G (p.Asn1384Ser) rs375716929
NM_004946.3(DOCK2):c.4162A>T (p.Met1388Leu) rs762466077
NM_004946.3(DOCK2):c.416A>T (p.Asp139Val)
NM_004946.3(DOCK2):c.4182G>A (p.Pro1394=) rs751200591
NM_004946.3(DOCK2):c.4361A>C (p.Asp1454Ala) rs779110995
NM_004946.3(DOCK2):c.4378G>A (p.Ala1460Thr) rs1554128971
NM_004946.3(DOCK2):c.4378G>T (p.Ala1460Ser)
NM_004946.3(DOCK2):c.4393G>C (p.Glu1465Gln)
NM_004946.3(DOCK2):c.4408G>A (p.Val1470Met)
NM_004946.3(DOCK2):c.4459A>G (p.Met1487Val) rs750831425
NM_004946.3(DOCK2):c.4467+4A>G
NM_004946.3(DOCK2):c.4468-5A>G
NM_004946.3(DOCK2):c.4512G>A (p.Thr1504=) rs376411478
NM_004946.3(DOCK2):c.4517A>G (p.Asn1506Ser)
NM_004946.3(DOCK2):c.4608C>A (p.Asp1536Glu)
NM_004946.3(DOCK2):c.4690G>A (p.Asp1564Asn)
NM_004946.3(DOCK2):c.4801C>T (p.Arg1601Trp)
NM_004946.3(DOCK2):c.4894C>T (p.Arg1632Cys)
NM_004946.3(DOCK2):c.4913G>A (p.Arg1638His)
NM_004946.3(DOCK2):c.5024C>T (p.Thr1675Met) rs201322810
NM_004946.3(DOCK2):c.5039A>G (p.Gln1680Arg) rs373168304
NM_004946.3(DOCK2):c.5074G>A (p.Glu1692Lys)
NM_004946.3(DOCK2):c.5083C>G (p.Leu1695Val) rs1561911758
NM_004946.3(DOCK2):c.5086C>T (p.Arg1696Trp) rs980056604
NM_004946.3(DOCK2):c.5087G>A (p.Arg1696Gln)
NM_004946.3(DOCK2):c.5129C>A (p.Ala1710Glu)
NM_004946.3(DOCK2):c.5129C>T (p.Ala1710Val) rs200684209
NM_004946.3(DOCK2):c.5165G>A (p.Arg1722Gln) rs199698060
NM_004946.3(DOCK2):c.5208G>A (p.Ser1736=) rs749522969
NM_004946.3(DOCK2):c.5221_5226del (p.Ile1741_Pro1742del) rs1561912393
NM_004946.3(DOCK2):c.5294C>T (p.Ala1765Val)
NM_004946.3(DOCK2):c.5317G>T (p.Gly1773Trp)
NM_004946.3(DOCK2):c.5324A>G (p.Asp1775Gly)
NM_004946.3(DOCK2):c.5335A>G (p.Thr1779Ala) rs2270898
NM_004946.3(DOCK2):c.533C>T (p.Thr178Ile)
NM_004946.3(DOCK2):c.5368C>T (p.Leu1790Phe) rs760479360
NM_004946.3(DOCK2):c.5390C>T (p.Thr1797Ile)
NM_004946.3(DOCK2):c.5431-10C>A rs1440481799
NM_004946.3(DOCK2):c.5431-7T>G rs1581583167
NM_004946.3(DOCK2):c.5439C>G (p.Ser1813Arg)
NM_004946.3(DOCK2):c.5462A>G (p.Gln1821Arg) rs1223159645
NM_004946.3(DOCK2):c.5483C>T (p.Thr1828Met)
NM_004946.3(DOCK2):c.566A>G (p.Glu189Gly) rs1234078639
NM_004946.3(DOCK2):c.615C>G (p.Asp205Glu)
NM_004946.3(DOCK2):c.679G>C (p.Val227Leu)
NM_004946.3(DOCK2):c.70G>C (p.Ala24Pro)
NM_004946.3(DOCK2):c.847C>T (p.Leu283Phe)
NM_004946.3(DOCK2):c.866A>G (p.Asn289Ser)
NM_004946.3(DOCK2):c.934_935delinsAA (p.Ala312Lys)
NM_004946.3(DOCK2):c.965C>A (p.Pro322His)

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