ClinVar Miner

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

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
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NM_004946.2(DOCK2):c.1843+9delG rs756542427
NM_004946.3(DOCK2):c.1215C>T (p.Thr405=) rs141406325
NM_004946.3(DOCK2):c.1360G>A (p.Ala454Thr) rs114888195
NM_004946.3(DOCK2):c.1555+10A>G rs373086704
NM_004946.3(DOCK2):c.1594G>A (p.Val532Met) rs149411090
NM_004946.3(DOCK2):c.2587A>G (p.Lys863Glu) rs141501849
NM_004946.3(DOCK2):c.3099A>G (p.Ala1033=) rs758385723
NM_004946.3(DOCK2):c.3468-5C>T rs371584556
NM_004946.3(DOCK2):c.3528C>T (p.Asn1176=) rs1554127501
NM_004946.3(DOCK2):c.3738C>A (p.Leu1246=) rs771448474
NM_004946.3(DOCK2):c.3741C>T (p.His1247=) rs144649763
NM_004946.3(DOCK2):c.3836C>T (p.Thr1279Met) rs145873210
NM_004946.3(DOCK2):c.44-9G>A rs778542070
NM_004946.3(DOCK2):c.4533G>T (p.Met1511Ile) rs148502872
NM_004946.3(DOCK2):c.5154G>A (p.Ser1718=) rs147230385
NM_004946.3(DOCK2):c.5259T>C (p.Phe1753=) rs138826774
NM_004946.3(DOCK2):c.5425A>G (p.Thr1809Ala) rs146886839
NM_004946.3(DOCK2):c.5446G>T (p.Ala1816Ser) rs144315682
NM_004946.3(DOCK2):c.90G>C (p.Gln30His) rs141894939

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