ClinVar Miner

List of variants reported as uncertain significance for DOCK2 deficiency by Invitae

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 60
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HGVS dbSNP
NM_004946.3(DOCK2):c.1057G>C (p.Val353Leu)
NM_004946.3(DOCK2):c.1288C>G (p.Leu430Val) rs370264550
NM_004946.3(DOCK2):c.1334A>G (p.Asn445Ser)
NM_004946.3(DOCK2):c.1349T>C (p.Met450Thr) rs759775916
NM_004946.3(DOCK2):c.1426T>C (p.Tyr476His) rs769211157
NM_004946.3(DOCK2):c.1486G>A (p.Ala496Thr)
NM_004946.3(DOCK2):c.148A>C (p.Ile50Leu) rs200852440
NM_004946.3(DOCK2):c.1540C>T (p.Arg514Trp)
NM_004946.3(DOCK2):c.1597A>G (p.Lys533Glu)
NM_004946.3(DOCK2):c.1742C>T (p.Thr581Met)
NM_004946.3(DOCK2):c.1753A>C (p.Ser585Arg)
NM_004946.3(DOCK2):c.1756T>C (p.Ser586Pro)
NM_004946.3(DOCK2):c.1843+6C>T rs374362264
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.2447+4A>G
NM_004946.3(DOCK2):c.2479C>T (p.Pro827Ser)
NM_004946.3(DOCK2):c.2525T>C (p.Ile842Thr)
NM_004946.3(DOCK2):c.2638C>A (p.Leu880Met) rs112062072
NM_004946.3(DOCK2):c.2656G>A (p.Val886Ile)
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.286T>C (p.Trp96Arg)
NM_004946.3(DOCK2):c.3140T>G (p.Phe1047Cys)
NM_004946.3(DOCK2):c.3233G>A (p.Gly1078Asp) rs1561883336
NM_004946.3(DOCK2):c.3310C>T (p.Arg1104Trp) rs780318765
NM_004946.3(DOCK2):c.3337G>A (p.Asp1113Asn)
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.3547G>A (p.Glu1183Lys)
NM_004946.3(DOCK2):c.3568G>A (p.Gly1190Ser)
NM_004946.3(DOCK2):c.360G>A (p.Met120Ile)
NM_004946.3(DOCK2):c.3683G>A (p.Arg1228His)
NM_004946.3(DOCK2):c.3794C>T (p.Thr1265Ile)
NM_004946.3(DOCK2):c.3854T>C (p.Ile1285Thr)
NM_004946.3(DOCK2):c.3986A>G (p.Tyr1329Cys) rs766635884
NM_004946.3(DOCK2):c.4018C>T (p.Pro1340Ser)
NM_004946.3(DOCK2):c.4060T>A (p.Ser1354Thr)
NM_004946.3(DOCK2):c.4147C>T (p.Pro1383Ser)
NM_004946.3(DOCK2):c.4151A>G (p.Asn1384Ser)
NM_004946.3(DOCK2):c.4162A>T (p.Met1388Leu)
NM_004946.3(DOCK2):c.4182G>A (p.Pro1394=)
NM_004946.3(DOCK2):c.4361A>C (p.Asp1454Ala)
NM_004946.3(DOCK2):c.4378G>A (p.Ala1460Thr) rs1554128971
NM_004946.3(DOCK2):c.4459A>G (p.Met1487Val)
NM_004946.3(DOCK2):c.4512G>A (p.Thr1504=)
NM_004946.3(DOCK2):c.5024C>T (p.Thr1675Met)
NM_004946.3(DOCK2):c.5039A>G (p.Gln1680Arg) rs373168304
NM_004946.3(DOCK2):c.5083C>G (p.Leu1695Val) rs1561911758
NM_004946.3(DOCK2):c.5086C>T (p.Arg1696Trp)
NM_004946.3(DOCK2):c.5129C>T (p.Ala1710Val)
NM_004946.3(DOCK2):c.5165G>A (p.Arg1722Gln)
NM_004946.3(DOCK2):c.5208G>A (p.Ser1736=)
NM_004946.3(DOCK2):c.5221_5226del (p.Ile1741_Pro1742del) rs1561912393
NM_004946.3(DOCK2):c.5335A>G (p.Thr1779Ala)
NM_004946.3(DOCK2):c.5368C>T (p.Leu1790Phe)
NM_004946.3(DOCK2):c.5431-10C>A
NM_004946.3(DOCK2):c.5431-7T>G
NM_004946.3(DOCK2):c.5462A>G (p.Gln1821Arg)
NM_004946.3(DOCK2):c.566A>G (p.Glu189Gly) rs1234078639

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