ClinVar Miner

List of variants in gene STX11 reported as likely benign for immune system disorder

Included ClinVar conditions (908):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 135
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HGVS dbSNP gnomAD frequency
NM_003764.4(STX11):c.*3670C>G rs79283142 0.01181
NM_003764.4(STX11):c.146G>A (p.Arg49Gln) rs17073498 0.00767
NM_003764.4(STX11):c.*1845C>T rs115419947 0.00646
NM_003764.4(STX11):c.799G>A (p.Val267Met) rs45574234 0.00545
NM_003764.4(STX11):c.*3298T>A rs75318897 0.00321
NM_003764.4(STX11):c.*4283G>A rs145148729 0.00321
NM_003764.4(STX11):c.546G>A (p.Glu182=) rs146949718 0.00274
NM_003764.4(STX11):c.*4070C>A rs148176592 0.00253
NM_003764.3(STX11):c.*4457G>A rs59612420 0.00250
NM_003764.4(STX11):c.839G>A (p.Cys280Tyr) rs34282765 0.00215
NM_003764.4(STX11):c.83C>T (p.Ser28Leu) rs143547259 0.00082
NM_003764.4(STX11):c.26T>G (p.Leu9Arg) rs34470310 0.00076
NM_003764.4(STX11):c.589G>A (p.Val197Met) rs141499372 0.00033
NM_003764.4(STX11):c.699G>C (p.Val233=) rs140973625 0.00018
NM_003764.4(STX11):c.729C>T (p.Asn243=) rs534184432 0.00010
NM_003764.4(STX11):c.831C>A (p.Thr277=) rs763282100 0.00006
NM_003764.4(STX11):c.423C>T (p.Arg141=) rs768985732 0.00004
NM_003764.4(STX11):c.651G>T (p.Leu217=) rs761372226 0.00004
NM_003764.4(STX11):c.738G>A (p.Glu246=) rs984613653 0.00004
NM_003764.4(STX11):c.237C>T (p.Leu79=) rs201775530 0.00003
NM_003764.4(STX11):c.573G>A (p.Glu191=) rs772078139 0.00003
NM_003764.4(STX11):c.183C>T (p.Asp61=) rs374922198 0.00002
NM_003764.4(STX11):c.585C>A (p.Ala195=) rs147525157 0.00002
NM_003764.4(STX11):c.105C>T (p.Phe35=) rs770690889 0.00001
NM_003764.4(STX11):c.15A>G (p.Leu5=) rs202220813 0.00001
NM_003764.4(STX11):c.387G>A (p.Arg129=) rs1802063048 0.00001
NM_003764.4(STX11):c.408C>A (p.Thr136=) rs780418852 0.00001
NM_003764.4(STX11):c.414C>T (p.Thr138=) rs1305403021 0.00001
NM_003764.4(STX11):c.570C>T (p.Ser190=) rs148354227 0.00001
NM_003764.4(STX11):c.675C>T (p.His225=) rs756608402 0.00001
NM_003764.4(STX11):c.798C>T (p.Ala266=) rs1487649315 0.00001
NM_003764.4(STX11):c.*1540dup rs149740241
NM_003764.4(STX11):c.*3036ATAA[1] rs146440209
NM_003764.4(STX11):c.*390T>C rs79627238
NM_003764.4(STX11):c.111G>C (p.Thr37=)
NM_003764.4(STX11):c.120C>T (p.Ile40=)
NM_003764.4(STX11):c.121C>T (p.Leu41=)
NM_003764.4(STX11):c.13C>T (p.Leu5=) rs1802043754
NM_003764.4(STX11):c.141C>T (p.Asp47=) rs752790166
NM_003764.4(STX11):c.156G>A (p.Gln52=)
NM_003764.4(STX11):c.172C>T (p.Leu58=)
NM_003764.4(STX11):c.174G>A (p.Leu58=)
NM_003764.4(STX11):c.174G>C (p.Leu58=)
NM_003764.4(STX11):c.180C>A (p.Ala60=)
NM_003764.4(STX11):c.180C>T (p.Ala60=) rs1222437687
NM_003764.4(STX11):c.189G>A (p.Lys63=)
NM_003764.4(STX11):c.193C>T (p.Leu65=) rs780525714
NM_003764.4(STX11):c.204G>A (p.Gln68=)
NM_003764.4(STX11):c.221C>T (p.Thr74Met) rs540150447
NM_003764.4(STX11):c.222G>A (p.Thr74=)
NM_003764.4(STX11):c.229C>A (p.Arg77=) rs778807808
NM_003764.4(STX11):c.243C>T (p.Ser81=)
NM_003764.4(STX11):c.246C>T (p.Ile82=)
NM_003764.4(STX11):c.255C>T (p.Asp85=) rs2128756929
NM_003764.4(STX11):c.258C>T (p.Thr86=) rs2128756931
NM_003764.4(STX11):c.264C>T (p.Ser88=) rs774895225
NM_003764.4(STX11):c.267C>T (p.Ile89=)
NM_003764.4(STX11):c.291C>T (p.Gly97=)
NM_003764.4(STX11):c.303C>T (p.His101=)
NM_003764.4(STX11):c.324G>A (p.Lys108=)
NM_003764.4(STX11):c.327G>A (p.Glu109=)
NM_003764.4(STX11):c.336G>A (p.Glu112=)
NM_003764.4(STX11):c.33G>A (p.Leu11=)
NM_003764.4(STX11):c.342T>A (p.Ala114=)
NM_003764.4(STX11):c.354C>T (p.His118=)
NM_003764.4(STX11):c.360G>A (p.Pro120=)
NM_003764.4(STX11):c.363C>T (p.His121=)
NM_003764.4(STX11):c.366G>C (p.Ser122=)
NM_003764.4(STX11):c.369A>G (p.Ala123=) rs763493074
NM_003764.4(STX11):c.36C>T (p.Ser12=)
NM_003764.4(STX11):c.384G>C (p.Ser128=)
NM_003764.4(STX11):c.402G>A (p.Ala134=)
NM_003764.4(STX11):c.405C>A (p.Leu135=)
NM_003764.4(STX11):c.405C>T (p.Leu135=)
NM_003764.4(STX11):c.423C>A (p.Arg141=) rs768985732
NM_003764.4(STX11):c.423C>G (p.Arg141=) rs768985732
NM_003764.4(STX11):c.426C>A (p.Ala142=)
NM_003764.4(STX11):c.432C>T (p.His144=)
NM_003764.4(STX11):c.435C>T (p.Asp145=) rs1802066250
NM_003764.4(STX11):c.447C>T (p.Ala149=)
NM_003764.4(STX11):c.459G>A (p.Gln153=)
NM_003764.4(STX11):c.489C>T (p.Arg163=)
NM_003764.4(STX11):c.492G>A (p.Gln164=)
NM_003764.4(STX11):c.513A>G (p.Glu171=)
NM_003764.4(STX11):c.516C>T (p.Val172=) rs2128757246
NM_003764.4(STX11):c.519G>A (p.Ser173=)
NM_003764.4(STX11):c.51G>A (p.Gln17=)
NM_003764.4(STX11):c.534G>A (p.Glu178=)
NM_003764.4(STX11):c.543C>T (p.Phe181=)
NM_003764.4(STX11):c.561C>T (p.Asp187=)
NM_003764.4(STX11):c.570C>G (p.Ser190=)
NM_003764.4(STX11):c.576C>T (p.Asn192=)
NM_003764.4(STX11):c.57C>T (p.Phe19=)
NM_003764.4(STX11):c.580C>T (p.Leu194=) rs2128757281
NM_003764.4(STX11):c.585C>G (p.Ala195=)
NM_003764.4(STX11):c.588C>T (p.Asp196=)
NM_003764.4(STX11):c.594G>A (p.Lys198=)
NM_003764.4(STX11):c.606C>A (p.Ala202=)
NM_003764.4(STX11):c.606C>G (p.Ala202=) rs781652788
NM_003764.4(STX11):c.612C>A (p.Leu204=)
NM_003764.4(STX11):c.618G>A (p.Glu206=)
NM_003764.4(STX11):c.621C>T (p.Ile207=)
NM_003764.4(STX11):c.624G>A (p.Glu208=)
NM_003764.4(STX11):c.630C>T (p.Arg210=)
NM_003764.4(STX11):c.633C>T (p.His211=)
NM_003764.4(STX11):c.63C>T (p.Asp21=) rs149176821
NM_003764.4(STX11):c.645G>C (p.Leu215=)
NM_003764.4(STX11):c.649C>T (p.Leu217=)
NM_003764.4(STX11):c.657C>T (p.Ser219=)
NM_003764.4(STX11):c.678G>A (p.Glu226=)
NM_003764.4(STX11):c.700C>T (p.Leu234=)
NM_003764.4(STX11):c.705G>A (p.Val235=)
NM_003764.4(STX11):c.708G>A (p.Glu236=)
NM_003764.4(STX11):c.717C>T (p.Ala239=)
NM_003764.4(STX11):c.720C>T (p.Asp240=)
NM_003764.4(STX11):c.732C>T (p.Val244=)
NM_003764.4(STX11):c.741C>A (p.Leu247=)
NM_003764.4(STX11):c.741C>T (p.Leu247=)
NM_003764.4(STX11):c.750A>G (p.Gln250=) rs1165149442
NM_003764.4(STX11):c.756G>A (p.Thr252=)
NM_003764.4(STX11):c.756G>C (p.Thr252=) rs1419598166
NM_003764.4(STX11):c.756G>T (p.Thr252=)
NM_003764.4(STX11):c.759C>A (p.Val253=)
NM_003764.4(STX11):c.768C>T (p.Thr256=)
NM_003764.4(STX11):c.780G>A (p.Lys260=)
NM_003764.4(STX11):c.801G>A (p.Val267=)
NM_003764.4(STX11):c.822C>T (p.Pro274=)
NM_003764.4(STX11):c.825C>T (p.Cys275=)
NM_003764.4(STX11):c.846C>T (p.Cys282=)
NM_003764.4(STX11):c.858C>A (p.Leu286=)
NM_003764.4(STX11):c.861G>A (p.Lys287=)
NM_003764.4(STX11):c.87C>T (p.Pro29=)
NM_003764.4(STX11):c.90C>T (p.His30=) rs751806887
NM_003764.4(STX11):c.93G>A (p.Glu31=)
NM_003764.4(STX11):c.96C>T (p.Asp32=) rs2128756763

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