ClinVar Miner

List of variants reported as uncertain significance for DOCK2 deficiency

Included ClinVar conditions (1):
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Total variants: 32
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HGVS dbSNP
NM_004946.2(DOCK2):c.1288C>G (p.Leu430Val) rs370264550
NM_004946.2(DOCK2):c.1349T>C (p.Met450Thr) rs759775916
NM_004946.2(DOCK2):c.1426T>C (p.Tyr476His) rs769211157
NM_004946.2(DOCK2):c.148A>C (p.Ile50Leu) rs200852440
NM_004946.2(DOCK2):c.1843+6C>T rs374362264
NM_004946.2(DOCK2):c.2638C>A (p.Leu880Met) rs112062072
NM_004946.2(DOCK2):c.2742G>C (p.Gln914His) rs761742890
NM_004946.2(DOCK2):c.338G>A (p.Arg113His) rs750421267
NM_004946.2(DOCK2):c.566A>G (p.Glu189Gly) rs1234078639
NM_004946.3(DOCK2):c.1742C>T (p.Thr581Met)
NM_004946.3(DOCK2):c.2051T>A (p.Ile684Asn)
NM_004946.3(DOCK2):c.2175C>G (p.Ser725Arg)
NM_004946.3(DOCK2):c.2656G>A (p.Val886Ile)
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)
NM_004946.3(DOCK2):c.3337G>A (p.Asp1113Asn)
NM_004946.3(DOCK2):c.3366T>A (p.Ser1122Arg) rs200973349
NM_004946.3(DOCK2):c.3683G>A (p.Arg1228His)
NM_004946.3(DOCK2):c.3854T>C (p.Ile1285Thr)
NM_004946.3(DOCK2):c.3986A>G (p.Tyr1329Cys) rs766635884
NM_004946.3(DOCK2):c.4151A>G (p.Asn1384Ser)
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.5039A>G (p.Gln1680Arg) rs373168304
NM_004946.3(DOCK2):c.5083C>G (p.Leu1695Val)
NM_004946.3(DOCK2):c.5129C>T (p.Ala1710Val)
NM_004946.3(DOCK2):c.5165G>A (p.Arg1722Gln)
NM_004946.3(DOCK2):c.5221_5226del (p.Ile1741_Pro1742del)
NM_004946.3(DOCK2):c.5335A>G (p.Thr1779Ala)

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