ClinVar Miner

List of variants in gene DOCK2 studied for not provided

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Gene type:
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Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_004946.3(DOCK2):c.2727G>A (p.Gln909=) rs261623 0.46437
NM_004946.3(DOCK2):c.3612C>T (p.Thr1204=) rs3763048 0.42784
NM_004946.3(DOCK2):c.3468-4G>A rs3763047 0.41818
NM_004946.3(DOCK2):c.3456C>G (p.Leu1152=) rs9791113 0.40563
NM_004946.3(DOCK2):c.4896T>C (p.Arg1632=) rs1045168 0.32381
NM_004946.3(DOCK2):c.3195A>C (p.Leu1065=) rs2287727 0.23497
NM_004946.3(DOCK2):c.1212C>A (p.Thr404=) rs2112703 0.16933
NM_004946.3(DOCK2):c.843+7G>A rs72841138 0.04984
NM_004946.3(DOCK2):c.2352A>G (p.Gln784=) rs13155521 0.04295
NM_004946.3(DOCK2):c.4295+9C>T rs115134653 0.00358
NM_004946.3(DOCK2):c.90G>C (p.Gln30His) rs141894939 0.00226
NM_004946.3(DOCK2):c.279G>T (p.Thr93=) rs144632263 0.00201
NM_004946.3(DOCK2):c.4201G>T (p.Ala1401Ser) rs143100569 0.00161
NM_004946.3(DOCK2):c.5446G>T (p.Ala1816Ser) rs144315682 0.00151
NM_004946.3(DOCK2):c.5484G>A (p.Thr1828=) rs140198889 0.00095
NM_004946.3(DOCK2):c.2638C>A (p.Leu880Met) rs112062072 0.00060
NM_004946.3(DOCK2):c.1594G>A (p.Val532Met) rs149411090 0.00058
NM_004946.3(DOCK2):c.1215C>T (p.Thr405=) rs141406325 0.00032
NM_004946.3(DOCK2):c.1742C>T (p.Thr581Met) rs140817788 0.00031
NM_004946.3(DOCK2):c.1896G>A (p.Glu632=) rs771194180 0.00023
NM_004946.3(DOCK2):c.3741C>T (p.His1247=) rs144649763 0.00008
NM_004946.3(DOCK2):c.2267+3G>A rs774041924 0.00006
NM_004946.3(DOCK2):c.2704-3C>T rs144101028 0.00006
NM_004946.3(DOCK2):c.286T>C (p.Trp96Arg) rs370949354 0.00006
NM_004946.3(DOCK2):c.5130G>A (p.Ala1710=) rs143741887 0.00006
NM_004946.3(DOCK2):c.3599G>A (p.Arg1200His) rs373428643 0.00004
NM_004946.3(DOCK2):c.3624+5G>A rs1321630215 0.00001
NM_004946.3(DOCK2):c.4162A>T (p.Met1388Leu) rs762466077 0.00001
NM_004946.3(DOCK2):c.5262C>T (p.Ala1754=) rs757478455 0.00001
NM_004946.3(DOCK2):c.5328G>A (p.Glu1776=) rs958464049 0.00001
NM_004946.3(DOCK2):c.169-30TTTTG[5]
NM_004946.3(DOCK2):c.1773dup (p.Leu592fs)
NM_004946.3(DOCK2):c.1843+8G>A rs1581082214
NM_004946.3(DOCK2):c.1929G>A (p.Glu643=) rs1581082786
NM_004946.3(DOCK2):c.2069A>C (p.Gln690Pro) rs1761963022
NM_004946.3(DOCK2):c.3073-8A>G rs113289730
NM_004946.3(DOCK2):c.5129C>T (p.Ala1710Val) rs200684209

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