ClinVar Miner

List of variants in gene INF2 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 117
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HGVS dbSNP gnomAD frequency
NM_022489.4(INF2):c.105C>T (p.Pro35=) rs4983530 0.98045
NM_022489.4(INF2):c.2640T>C (p.Asp880=) rs10133301 0.88251
NM_022489.4(INF2):c.2611-122G>C rs4497619 0.85993
NM_022489.4(INF2):c.1+171A>G rs4247030 0.81791
NM_022489.4(INF2):c.3066T>C (p.Asp1022=) rs4983535 0.79980
NM_022489.4(INF2):c.3041-56C>T rs9672043 0.79898
NM_022489.4(INF2):c.2490-292T>C rs4983534 0.76476
NM_022489.4(INF2):c.2239+256G>A rs12882277 0.66145
NM_022489.4(INF2):c.2489+117C>T rs4983533 0.59331
NM_022489.4(INF2):c.2489+53T>C rs4983531 0.58773
NM_022489.4(INF2):c.2489+62G>C rs4983532 0.58722
NM_022489.4(INF2):c.2310+8del rs3840006 0.58720
NM_022489.4(INF2):c.2611-84G>A rs10144190 0.53555
NM_022489.4(INF2):c.*536G>T rs1128880 0.46956
NM_022489.4(INF2):c.391+321C>T rs11160817 0.45936
NM_022489.4(INF2):c.1+174C>T rs4247031 0.45277
NM_022489.4(INF2):c.1950-231C>T rs73345596 0.27583
NM_022489.4(INF2):c.2239+157T>C rs56322618 0.23358
NM_022489.4(INF2):c.668-31G>A rs7145851 0.19890
NM_022489.4(INF2):c.*2-48_*2-47del rs138798126 0.17981
NM_022489.4(INF2):c.668-90G>A rs7145815 0.17628
NM_022489.4(INF2):c.668-78T>G rs7146817 0.17531
NM_022489.4(INF2):c.1949+171G>A rs533346206 0.16061
NM_022489.4(INF2):c.1949+170del rs67389203 0.16058
NM_022489.4(INF2):c.*437G>A rs1128866 0.15838
NM_022489.4(INF2):c.1736-175C>T rs113514625 0.11854
NM_022489.4(INF2):c.702-57G>A rs79559717 0.11794
NM_022489.4(INF2):c.668-32C>T rs7145566 0.07464
NM_022489.4(INF2):c.1735+106G>A rs114087680 0.06552
NM_022489.4(INF2):c.2775+15C>T rs73347508 0.06278
NM_022489.4(INF2):c.3286C>T (p.Pro1096Ser) rs34251364 0.05945
NM_022489.4(INF2):c.1736-51G>A rs117034570 0.05877
NM_022489.4(INF2):c.668-140_668-135del rs199612689 0.05874
NM_022489.4(INF2):c.843+16C>T rs118017785 0.05808
NM_022489.4(INF2):c.668-144_668-142del rs374945781 0.05793
NM_022489.4(INF2):c.844-36C>T rs7142337 0.05364
NM_022489.4(INF2):c.2418+43C>A rs60660079 0.05051
NM_022489.4(INF2):c.3041-75G>A rs13379430 0.04818
NM_022489.4(INF2):c.1227G>T (p.Ser409=) rs3809455 0.03433
NM_022489.4(INF2):c.*2-278G>A rs79826755 0.03152
NM_022489.4(INF2):c.2878+61C>T rs73347510 0.02736
NM_022489.4(INF2):c.1+185C>T rs74395064 0.02622
NM_022489.4(INF2):c.2322C>T (p.Thr774=) rs59751492 0.02373
NM_022489.4(INF2):c.2489+292C>T rs112598276 0.02133
NM_022489.4(INF2):c.391+18A>T rs115458897 0.02077
NM_022489.4(INF2):c.3478G>A (p.Gly1160Ser) rs9672065 0.01930
NM_022489.4(INF2):c.*553T>C rs115685078 0.01713
NM_022489.4(INF2):c.392-184G>A rs115735784 0.01549
NM_022489.4(INF2):c.2571C>T (p.Ser857=) rs62640005 0.01396
NM_022489.4(INF2):c.42G>A (p.Leu14=) rs62638758 0.01192
NM_022489.4(INF2):c.3153C>T (p.Asp1051=) rs117457867 0.01185
NM_022489.4(INF2):c.391+17G>A rs4074531 0.01087
NM_022489.4(INF2):c.1452T>C (p.Cys484=) rs371775604 0.01021
NM_022489.4(INF2):c.1281_1286del (p.Pro428_Leu429del) rs751555478 0.00781
NM_022489.4(INF2):c.2630G>A (p.Arg877Gln) rs142678449 0.00777
NM_022489.4(INF2):c.1269A>C (p.Pro423=) rs750660584 0.00746
NM_022489.4(INF2):c.1547C>T (p.Pro516Leu) rs111589086 0.00721
NM_022489.4(INF2):c.*10C>T rs142710295 0.00580
NM_022489.4(INF2):c.879G>A (p.Ser293=) rs184709736 0.00538
NM_022489.4(INF2):c.3108T>C (p.Leu1036=) rs186075307 0.00518
NM_022489.4(INF2):c.1078G>A (p.Val360Ile) rs114820975 0.00483
NM_022489.4(INF2):c.3069C>T (p.Pro1023=) rs75382114 0.00477
NM_022489.4(INF2):c.1451G>A (p.Cys484Tyr) rs201323100 0.00470
NM_022489.4(INF2):c.3404C>T (p.Thr1135Met) rs3803311 0.00288
NM_022489.4(INF2):c.*544G>A rs111978619 0.00287
NM_022489.4(INF2):c.3078C>T (p.Ser1026=) rs377023270 0.00260
NM_022489.4(INF2):c.-9-37C>T rs142345234 0.00252
NM_022489.4(INF2):c.1049C>T (p.Pro350Leu) rs146529868 0.00250
NM_022489.4(INF2):c.2458C>T (p.Arg820Trp) rs79327775 0.00247
NM_022489.4(INF2):c.2999G>A (p.Ser1000Asn) rs148541427 0.00214
NM_022489.4(INF2):c.2138+9G>A rs201065953 0.00213
NM_022489.4(INF2):c.*638G>A rs191976493 0.00182
NM_022489.4(INF2):c.1735+42G>A rs190829431 0.00175
NM_022489.4(INF2):c.2490-20C>T rs187104422 0.00170
NM_022489.4(INF2):c.2490-32G>A rs199892463 0.00154
NM_022489.4(INF2):c.264C>T (p.Gly88=) rs201587219 0.00150
NM_022489.4(INF2):c.3244G>T (p.Ala1082Ser) rs143540449 0.00150
NM_022489.4(INF2):c.558C>T (p.Ser186=) rs150714865 0.00149
NM_022489.4(INF2):c.1281A>C (p.Pro427=) rs754332692 0.00140
NM_022489.4(INF2):c.1736-48A>G rs200316139 0.00122
NM_022489.4(INF2):c.3612G>A (p.Ser1204=) rs150811244 0.00121
NM_022489.4(INF2):c.1732C>T (p.Arg578Cys) rs201593594 0.00116
NM_022489.4(INF2):c.2879-27G>A rs202124201 0.00103
NM_022489.4(INF2):c.2848C>T (p.Arg950Trp) rs199873407 0.00098
NM_022489.4(INF2):c.507+7G>A rs201568246 0.00088
NM_022489.4(INF2):c.1950-10C>T rs199987321 0.00081
NM_022489.4(INF2):c.*136C>T rs150579444 0.00053
NM_022489.4(INF2):c.1144A>G (p.Ser382Gly) rs201077878 0.00048
NM_022489.4(INF2):c.*2-29A>G rs374763306 0.00036
NM_022489.4(INF2):c.37G>A (p.Ala13Thr) rs201383094 0.00034
NM_022489.4(INF2):c.2509C>T (p.Arg837Cys) rs201534539 0.00031
NM_022489.4(INF2):c.3684G>A (p.Arg1228=) rs189263181 0.00019
NM_022489.4(INF2):c.2479C>A (p.Gln827Lys) rs4983379 0.00014
NM_022489.4(INF2):c.1755G>A (p.Ala585=) rs375573206 0.00013
NM_022489.4(INF2):c.1736-41G>A rs757125435 0.00011
NM_022489.4(INF2):c.3040+21C>T rs368662410 0.00011
NM_022489.4(INF2):c.1499C>T (p.Pro500Leu) rs561201601 0.00009
NM_022489.4(INF2):c.1448C>T (p.Ser483Phe) rs753188664 0.00006
NM_022489.4(INF2):c.2517G>A (p.Glu839=) rs561061092 0.00002
NM_022489.4(INF2):c.*2-294A>G rs4247033
NM_022489.4(INF2):c.*25A>G rs541048885
NM_022489.4(INF2):c.1262CACCCC[2] (p.Pro425_Pro428del) rs573567814
NM_022489.4(INF2):c.1262CACCCC[3] (p.Pro427_Pro428del) rs573567814
NM_022489.4(INF2):c.1275A>C (p.Pro425=) rs760828390
NM_022489.4(INF2):c.1582C>T (p.Pro528Ser) rs181694819
NM_022489.4(INF2):c.1736-38dup rs149923432
NM_022489.4(INF2):c.2239+170del rs34003576
NM_022489.4(INF2):c.2507T>C (p.Ile836Thr) rs767351070
NM_022489.4(INF2):c.3040+286C>A rs76501953
NM_022489.4(INF2):c.3041-146C>G rs118061751
NM_022489.4(INF2):c.3207A>C (p.Pro1069=) rs1128840
NM_022489.4(INF2):c.3207A>G (p.Pro1069=) rs1128840
NM_022489.4(INF2):c.391+6C>T rs75115369
NM_022489.4(INF2):c.667+212T>G rs7146454
NM_022489.4(INF2):c.843+239G>A rs75458917
NM_022489.4(INF2):c.985+66G>A rs57402537
NM_022489.4(INF2):c.985+66G>C rs57402537

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