ClinVar Miner

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

Included ClinVar conditions (1):
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Gene type:
ClinVar version:
Total variants: 40
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HGVS dbSNP
NM_004946.3(DOCK2):c.1133-4G>T rs201185913
NM_004946.3(DOCK2):c.1215C>T (p.Thr405=) rs141406325
NM_004946.3(DOCK2):c.127+6T>A rs757957020
NM_004946.3(DOCK2):c.1316A>G (p.Asn439Ser) rs113673055
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.1603A>G (p.Met535Val) rs143942535
NM_004946.3(DOCK2):c.1743G>A (p.Thr581=) rs201495849
NM_004946.3(DOCK2):c.1843+9del rs756542427
NM_004946.3(DOCK2):c.221G>A (p.Arg74Lys) rs368156237
NM_004946.3(DOCK2):c.2436G>C (p.Ala812=) rs761164114
NM_004946.3(DOCK2):c.2587A>G (p.Lys863Glu) rs141501849
NM_004946.3(DOCK2):c.2939T>C (p.Ile980Thr) rs148694888
NM_004946.3(DOCK2):c.3057G>C (p.Thr1019=) rs150071550
NM_004946.3(DOCK2):c.3057G>T (p.Thr1019=) rs150071550
NM_004946.3(DOCK2):c.3099A>G (p.Ala1033=) rs758385723
NM_004946.3(DOCK2):c.3438C>T (p.Asp1146=) rs181479183
NM_004946.3(DOCK2):c.3468-5C>T rs371584556
NM_004946.3(DOCK2):c.3636A>G (p.Lys1212=) rs1581545501
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.3843C>T (p.Tyr1281=) rs151251345
NM_004946.3(DOCK2):c.3924C>T (p.Tyr1308=) rs747703876
NM_004946.3(DOCK2):c.4201G>T (p.Ala1401Ser) rs143100569
NM_004946.3(DOCK2):c.4341C>T (p.Pro1447=) rs181184602
NM_004946.3(DOCK2):c.44-9G>A rs778542070
NM_004946.3(DOCK2):c.4533G>T (p.Met1511Ile) rs148502872
NM_004946.3(DOCK2):c.4728+10C>T rs201994696
NM_004946.3(DOCK2):c.4878C>T (p.Asp1626=) rs201318538
NM_004946.3(DOCK2):c.5027C>G (p.Pro1676Arg) rs150108225
NM_004946.3(DOCK2):c.5048C>T (p.Pro1683Leu) rs184196863
NM_004946.3(DOCK2):c.5049G>A (p.Pro1683=) rs201405765
NM_004946.3(DOCK2):c.5079C>G (p.Val1693=) rs146935890
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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