ClinVar Miner

List of variants in gene DOCK8 reported as likely benign for not specified

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Gene type:
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Total variants: 60
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HGVS dbSNP
NM_203447.3(DOCK8):c.-12C>T rs769683861
NM_203447.3(DOCK8):c.1017G>A (p.Pro339=) rs35746964
NM_203447.3(DOCK8):c.1044+12C>T rs376502656
NM_203447.3(DOCK8):c.1045-17A>T rs754140228
NM_203447.3(DOCK8):c.12G>T (p.Leu4=) rs753215803
NM_203447.3(DOCK8):c.1422+17C>T rs200839477
NM_203447.3(DOCK8):c.1516+16C>G rs141986056
NM_203447.3(DOCK8):c.1517-6_1517-5delCT rs1064794460
NM_203447.3(DOCK8):c.156+1383T>C rs150314778
NM_203447.3(DOCK8):c.1587C>G (p.Pro529=) rs146289269
NM_203447.3(DOCK8):c.1798-10T>C rs373312047
NM_203447.3(DOCK8):c.1839A>G (p.Glu613=) rs377593459
NM_203447.3(DOCK8):c.1863T>C (p.His621=) rs1057523014
NM_203447.3(DOCK8):c.1881T>C (p.Phe627=) rs140134223
NM_203447.3(DOCK8):c.2346C>T (p.Ser782=) rs562630401
NM_203447.3(DOCK8):c.2427C>T (p.Ile809=) rs772977760
NM_203447.3(DOCK8):c.2440+12C>G rs747420278
NM_203447.3(DOCK8):c.2440+13_2440+22delAGGGCTGGGC rs769837178
NM_203447.3(DOCK8):c.2634G>A (p.Arg878=) rs370632366
NM_203447.3(DOCK8):c.2874+12_2874+13delAG rs1182917562
NM_203447.3(DOCK8):c.2970+16G>A rs377526583
NM_203447.3(DOCK8):c.2971-4G>A rs186097329
NM_203447.3(DOCK8):c.2971-6C>T rs773500215
NM_203447.3(DOCK8):c.3058A>G (p.Ile1020Val) rs151094543
NM_203447.3(DOCK8):c.3234+12C>T rs567265382
NM_203447.3(DOCK8):c.3234+15_3234+16insCA rs1554691268
NM_203447.3(DOCK8):c.3234+15delC rs375864618
NM_203447.3(DOCK8):c.3263C>T (p.Thr1088Met) rs149065013
NM_203447.3(DOCK8):c.332+9T>G rs113744378
NM_203447.3(DOCK8):c.333-12C>G rs1057521494
NM_203447.3(DOCK8):c.3543A>G (p.Val1181=) rs753242273
NM_203447.3(DOCK8):c.3636C>T (p.Ala1212=) rs745506610
NM_203447.3(DOCK8):c.3701-17C>T rs376111035
NM_203447.3(DOCK8):c.378C>G (p.Ile126Met) rs141175202
NM_203447.3(DOCK8):c.380G>A (p.Arg127His) rs150742426
NM_203447.3(DOCK8):c.3813A>G (p.Lys1271=) rs75411647
NM_203447.3(DOCK8):c.3826G>T (p.Val1276Leu) rs148796842
NM_203447.3(DOCK8):c.3841-11C>T rs372829200
NM_203447.3(DOCK8):c.393C>T (p.Ile131=) rs139097471
NM_203447.3(DOCK8):c.4019A>G (p.Tyr1340Cys) rs116920018
NM_203447.3(DOCK8):c.4024-4C>T rs111306749
NM_203447.3(DOCK8):c.4158C>T (p.Asn1386=) rs77803650
NM_203447.3(DOCK8):c.4241+16A>G rs142428536
NM_203447.3(DOCK8):c.4346C>T (p.Ser1449Leu) rs370123223
NM_203447.3(DOCK8):c.4491C>T (p.Phe1497=) rs7854035
NM_203447.3(DOCK8):c.4627-3C>T rs368566107
NM_203447.3(DOCK8):c.477G>A (p.Pro159=) rs375091035
NM_203447.3(DOCK8):c.4998G>C (p.Val1666=) rs370901183
NM_203447.3(DOCK8):c.5079+7dupT rs762095035
NM_203447.3(DOCK8):c.5355+6C>T rs188141951
NM_203447.3(DOCK8):c.5481T>C (p.His1827=) rs1554708887
NM_203447.3(DOCK8):c.5781C>T (p.Tyr1927=) rs138225192
NM_203447.3(DOCK8):c.580G>A (p.Val194Ile) rs141210649
NM_203447.3(DOCK8):c.6068+18T>C rs1480534000
NM_203447.3(DOCK8):c.6138C>G (p.Leu2046=) rs139515839
NM_203447.3(DOCK8):c.6201A>G (p.Glu2067=) rs145573166
NM_203447.3(DOCK8):c.741+16T>G rs746933009
NM_203447.3(DOCK8):c.870C>G (p.Leu290=) rs201244929
NM_203447.3(DOCK8):c.895-9C>T rs1057523638
NM_203447.3(DOCK8):c.963T>A (p.Pro321=) rs1057521177

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