ClinVar Miner

List of variants in gene DOCK2 reported as benign for DOCK2 deficiency

Included ClinVar conditions (1):
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Gene type:
ClinVar version:
Total variants: 25
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HGVS dbSNP
NM_004946.3(DOCK2):c.1417A>G (p.Met473Val) rs201626676
NM_004946.3(DOCK2):c.1767T>G (p.Val589=) rs34864600
NM_004946.3(DOCK2):c.2199C>T (p.Ile733=) rs35530753
NM_004946.3(DOCK2):c.2241T>C (p.Ile747=) rs35887608
NM_004946.3(DOCK2):c.2352A>G (p.Gln784=) rs13155521
NM_004946.3(DOCK2):c.279G>T (p.Thr93=) rs144632263
NM_004946.3(DOCK2):c.2946G>A (p.Lys982=) rs36028557
NM_004946.3(DOCK2):c.3192G>T (p.Arg1064=) rs58980222
NM_004946.3(DOCK2):c.3417G>A (p.Glu1139=) rs149853735
NM_004946.3(DOCK2):c.366C>T (p.Tyr122=) rs35393134
NM_004946.3(DOCK2):c.3828G>C (p.Leu1276=) rs6555882
NM_004946.3(DOCK2):c.3945T>C (p.Tyr1315=) rs34133853
NM_004946.3(DOCK2):c.4295+9C>T rs115134653
NM_004946.3(DOCK2):c.4314C>T (p.Tyr1438=) rs17647491
NM_004946.3(DOCK2):c.4729-4C>T rs115841644
NM_004946.3(DOCK2):c.4955A>G (p.Asn1652Ser) rs113216049
NM_004946.3(DOCK2):c.4976G>C (p.Ser1659Thr) rs139644615
NM_004946.3(DOCK2):c.5295G>A (p.Ala1765=) rs370911923
NM_004946.3(DOCK2):c.5344C>T (p.Arg1782Cys) rs149343589
NM_004946.3(DOCK2):c.5445G>A (p.Ser1815=) rs200128185
NM_004946.3(DOCK2):c.5475G>A (p.Ser1825=) rs114098294
NM_004946.3(DOCK2):c.631A>G (p.Met211Val) rs151191554
NM_004946.3(DOCK2):c.752C>T (p.Thr251Met) rs78243868
NM_004946.3(DOCK2):c.753G>A (p.Thr251=) rs146746458
NM_004946.3(DOCK2):c.843+7G>A rs72841138

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