ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_203447.4(DOCK8):c.5908G>C (p.Ala1970Pro) rs34908836 0.07052
NM_203447.4(DOCK8):c.3701-17C>T rs376111035 0.00409
NM_203447.4(DOCK8):c.156+1383T>C rs150314778 0.00354
NM_203447.4(DOCK8):c.4019A>G (p.Tyr1340Cys) rs116920018 0.00276
NM_203447.4(DOCK8):c.4491= (p.Phe1497=) rs7854035 0.00274
NM_203447.4(DOCK8):c.1516+16C>G rs141986056 0.00266
NM_203447.4(DOCK8):c.6201A>G (p.Glu2067=) rs145573166 0.00221
NM_203447.4(DOCK8):c.2310G>A (p.Glu770=) rs116175117 0.00217
NM_203447.4(DOCK8):c.528+7C>A rs114833839 0.00207
NM_203447.4(DOCK8):c.380G>A (p.Arg127His) rs150742426 0.00196
NM_203447.4(DOCK8):c.4024-4C>T rs111306749 0.00196
NM_203447.4(DOCK8):c.4158C>T (p.Asn1386=) rs77803650 0.00195
NM_203447.4(DOCK8):c.3460C>T (p.Arg1154Cys) rs34390308 0.00170
NM_203447.4(DOCK8):c.378C>G (p.Ile126Met) rs141175202 0.00124
NM_203447.4(DOCK8):c.5781C>T (p.Tyr1927=) rs138225192 0.00122
NM_203447.4(DOCK8):c.3826G>T (p.Val1276Leu) rs148796842 0.00120
NM_203447.4(DOCK8):c.3813A>G (p.Lys1271=) rs75411647 0.00115
NM_203447.4(DOCK8):c.580G>A (p.Val194Ile) rs141210649 0.00097
NM_203447.4(DOCK8):c.1422+17C>T rs200839477 0.00071
NM_203447.4(DOCK8):c.3263C>T (p.Thr1088Met) rs149065013 0.00067
NM_203447.4(DOCK8):c.3023G>A (p.Arg1008Gln) rs145844320 0.00064
NM_203447.4(DOCK8):c.1798-10T>C rs373312047 0.00059
NM_203447.4(DOCK8):c.5355+6C>T rs188141951 0.00046
NM_203447.4(DOCK8):c.828-7A>G rs200243583 0.00030
NM_203447.4(DOCK8):c.1839A>G (p.Glu613=) rs377593459 0.00027
NM_203447.4(DOCK8):c.5892C>T (p.Asn1964=) rs138617736 0.00023
NM_203447.4(DOCK8):c.1119T>C (p.Gly373=) rs370564355 0.00021
NM_203447.4(DOCK8):c.3234+12C>T rs567265382 0.00020
NM_203447.4(DOCK8):c.5223+15G>T rs574618395 0.00019
NM_203447.4(DOCK8):c.1044+12C>T rs376502656 0.00016
NM_203447.4(DOCK8):c.1800C>A (p.Val600=) rs148177924 0.00013
NM_203447.4(DOCK8):c.4998G>C (p.Val1666=) rs370901183 0.00013
NM_203447.4(DOCK8):c.2970+16G>A rs377526583 0.00012
NM_203447.4(DOCK8):c.4241+16A>G rs142428536 0.00011
NM_203447.4(DOCK8):c.6138C>G (p.Leu2046=) rs139515839 0.00011
NM_203447.4(DOCK8):c.2634G>A (p.Arg878=) rs370632366 0.00009
NM_203447.4(DOCK8):c.4627-3C>T rs368566107 0.00009
NM_203447.4(DOCK8):c.5079+7dup rs762095035 0.00009
NM_203447.4(DOCK8):c.3543A>G (p.Val1181=) rs753242273 0.00008
NM_203447.4(DOCK8):c.393C>T (p.Ile131=) rs139097471 0.00008
NM_203447.4(DOCK8):c.1868+6T>C rs777072262 0.00006
NM_203447.4(DOCK8):c.477G>A (p.Pro159=) rs375091035 0.00005
NM_203447.4(DOCK8):c.741+16T>G rs746933009 0.00005
NM_203447.4(DOCK8):c.5820T>C (p.Phe1940=) rs768939248 0.00004
NM_203447.4(DOCK8):c.-12C>T rs769683861 0.00003
NM_203447.4(DOCK8):c.1863T>C (p.His621=) rs1057523014 0.00003
NM_203447.4(DOCK8):c.6068+18T>C rs1480534000 0.00003
NM_203447.4(DOCK8):c.2971-6C>T rs773500215 0.00002
NM_203447.4(DOCK8):c.1045-17A>T rs754140228 0.00001
NM_203447.4(DOCK8):c.2346C>T (p.Ser782=) rs562630401 0.00001
NM_203447.4(DOCK8):c.2427C>T (p.Ile809=) rs772977760 0.00001
NM_203447.4(DOCK8):c.3636C>T (p.Ala1212=) rs745506610 0.00001
NM_203447.4(DOCK8):c.870C>G (p.Leu290=) rs201244929 0.00001
NM_203447.4(DOCK8):c.895-9C>T rs1057523638 0.00001
NM_203447.4(DOCK8):c.1517-11TC[2] rs1064794460
NM_203447.4(DOCK8):c.2440+12C>G rs747420278
NM_203447.4(DOCK8):c.2440+13_2440+22del rs769837178
NM_203447.4(DOCK8):c.2874+8AG[2] rs1182917562
NM_203447.4(DOCK8):c.3234+15_3234+16insCA rs1554691268
NM_203447.4(DOCK8):c.3234+15del rs375864618
NM_203447.4(DOCK8):c.333-12C>G rs1057521494
NM_203447.4(DOCK8):c.4563C>T (p.Val1521=) rs370171781
NM_203447.4(DOCK8):c.5205C>A (p.Ala1735=) rs150682688
NM_203447.4(DOCK8):c.53+14del rs749863710
NM_203447.4(DOCK8):c.5481T>C (p.His1827=) rs1554708887
NM_203447.4(DOCK8):c.963T>A (p.Pro321=) rs1057521177

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