ClinVar Miner

List of variants in gene INF2 studied for Focal segmental glomerulosclerosis 5

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Gene type:
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Total variants: 149
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HGVS dbSNP gnomAD frequency
NM_022489.4(INF2):c.105C>T (p.Pro35=) rs4983530 0.98049
NM_022489.4(INF2):c.2640T>C (p.Asp880=) rs10133301 0.88426
NM_022489.4(INF2):c.3066T>C (p.Asp1022=) rs4983535 0.79980
NM_022489.4(INF2):c.*536G>T rs1128880 0.45873
NM_022489.4(INF2):c.*437G>A rs1128866 0.16086
NM_022489.4(INF2):c.2775+15C>T rs73347508 0.06749
NM_022489.4(INF2):c.-10G>A rs115602636 0.05904
NM_022489.4(INF2):c.3286C>T (p.Pro1096Ser) rs34251364 0.05864
NM_022489.4(INF2):c.1227G>T (p.Ser409=) rs3809455 0.03433
NM_022489.4(INF2):c.2322C>T (p.Thr774=) rs59751492 0.02373
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.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.1452T>C (p.Cys484=) rs371775604 0.01071
NM_022489.4(INF2):c.2630G>A (p.Arg877Gln) rs142678449 0.00781
NM_022489.4(INF2):c.1269A>C (p.Pro423=) rs750660584 0.00746
NM_022489.4(INF2):c.*10C>T rs142710295 0.00580
NM_022489.4(INF2):c.879G>A (p.Ser293=) rs184709736 0.00543
NM_022489.4(INF2):c.3108T>C (p.Leu1036=) rs186075307 0.00532
NM_022489.4(INF2):c.1078G>A (p.Val360Ile) rs114820975 0.00483
NM_022489.4(INF2):c.1263A>C (p.Pro421=) rs761903419 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.*388A>G rs140513391 0.00296
NM_022489.4(INF2):c.*544G>A rs111978619 0.00287
NM_022489.4(INF2):c.3078C>T (p.Ser1026=) rs377023270 0.00272
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.3404C>T (p.Thr1135Met) rs3803311 0.00242
NM_022489.4(INF2):c.*638G>A rs191976493 0.00182
NM_022489.4(INF2):c.3694+13G>C rs776214809 0.00163
NM_022489.4(INF2):c.558C>T (p.Ser186=) rs150714865 0.00158
NM_022489.4(INF2):c.1647A>G (p.Ala549=) rs201674759 0.00143
NM_022489.4(INF2):c.3134G>A (p.Arg1045Gln) rs200369827 0.00126
NM_022489.4(INF2):c.2848C>T (p.Arg950Trp) rs199873407 0.00098
NM_022489.4(INF2):c.507+7G>A rs201568246 0.00095
NM_022489.4(INF2):c.1950-10C>T rs199987321 0.00082
NM_022489.4(INF2):c.1329A>C (p.Pro443=) rs769756576 0.00062
NM_022489.4(INF2):c.*16C>T rs199912466 0.00058
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.*803G>A rs555692643 0.00041
NM_022489.4(INF2):c.3221G>A (p.Arg1074Lys) rs201445955 0.00036
NM_022489.4(INF2):c.37G>A (p.Ala13Thr) rs201383094 0.00034
NM_022489.4(INF2):c.2509C>T (p.Arg837Cys) rs201534539 0.00033
NM_022489.4(INF2):c.609C>T (p.Ala203=) rs140017506 0.00028
NM_022489.4(INF2):c.2885A>C (p.Lys962Thr) rs376067427 0.00023
NM_022489.4(INF2):c.3563C>T (p.Ser1188Phe) rs201715539 0.00022
NM_022489.4(INF2):c.3103G>A (p.Gly1035Ser) rs368995122 0.00019
NM_022489.4(INF2):c.2053A>G (p.Ile685Val) rs199526439 0.00016
NM_022489.4(INF2):c.3206C>T (p.Pro1069Leu) rs376139171 0.00014
NM_022489.4(INF2):c.3684G>A (p.Arg1228=) rs189263181 0.00014
NM_022489.4(INF2):c.1755G>A (p.Ala585=) rs375573206 0.00013
NM_022489.4(INF2):c.966C>T (p.Ala322=) rs774024906 0.00013
NM_022489.4(INF2):c.1264C>T (p.Pro422Ser) rs767748953 0.00012
NM_022489.4(INF2):c.1360C>T (p.Leu454Phe) rs545495465 0.00012
NM_022489.4(INF2):c.3550G>A (p.Ala1184Thr) rs374684004 0.00012
NM_022489.4(INF2):c.1770C>T (p.Pro590=) rs549506051 0.00011
NM_022489.4(INF2):c.1978C>T (p.Arg660Trp) rs138577569 0.00011
NM_022489.4(INF2):c.474C>T (p.His158=) rs141172921 0.00010
NM_022489.4(INF2):c.1197C>T (p.His399=) rs746493706 0.00009
NM_022489.4(INF2):c.1499C>T (p.Pro500Leu) rs561201601 0.00009
NM_022489.4(INF2):c.1640G>A (p.Gly547Asp) rs376451593 0.00009
NM_022489.4(INF2):c.1806C>T (p.Ile602=) rs760506368 0.00009
NM_022489.4(INF2):c.2053-13C>T rs753775095 0.00009
NM_022489.4(INF2):c.3654C>T (p.Thr1218=) rs557462297 0.00009
NM_022489.4(INF2):c.798C>G (p.Val266=) rs375005967 0.00009
NM_022489.4(INF2):c.*1+1G>C rs758452999 0.00007
NM_022489.4(INF2):c.597C>T (p.Ser199=) rs372269719 0.00007
NM_022489.4(INF2):c.*447A>T rs749782054 0.00006
NM_022489.4(INF2):c.1448C>T (p.Ser483Phe) rs753188664 0.00006
NM_022489.4(INF2):c.2423C>T (p.Ala808Val) rs200948588 0.00006
NM_022489.4(INF2):c.2459G>A (p.Arg820Gln) rs759989953 0.00006
NM_022489.4(INF2):c.885G>A (p.Leu295=) rs370680236 0.00006
NM_022489.4(INF2):c.*311T>A rs975205957 0.00005
NM_022489.4(INF2):c.1587C>T (p.Pro529=) rs755649066 0.00005
NM_022489.4(INF2):c.2440G>A (p.Asp814Asn) rs373532334 0.00005
NM_022489.4(INF2):c.510G>A (p.Thr170=) rs750711173 0.00004
NM_022489.4(INF2):c.*314G>A rs921070326 0.00003
NM_022489.4(INF2):c.2201T>G (p.Val734Gly) rs754128624 0.00003
NM_022489.4(INF2):c.2847G>A (p.Ala949=) rs754546219 0.00003
NM_022489.4(INF2):c.3590C>T (p.Ala1197Val) rs372714774 0.00003
NM_022489.4(INF2):c.*288C>T rs534561202 0.00002
NM_022489.4(INF2):c.1139A>G (p.Lys380Arg) rs762096939 0.00002
NM_022489.4(INF2):c.1865G>A (p.Arg622Gln) rs200155666 0.00002
NM_022489.4(INF2):c.18C>T (p.Gly6=) rs1032255653 0.00002
NM_022489.4(INF2):c.2775+13G>A rs759589756 0.00002
NM_022489.4(INF2):c.3040+2T>C rs1437272364 0.00002
NM_022489.4(INF2):c.3703C>T (p.Pro1235Ser) rs201091360 0.00002
NM_022489.4(INF2):c.*153C>T rs899450753 0.00001
NM_022489.4(INF2):c.*232G>A rs886050384 0.00001
NM_022489.4(INF2):c.*289G>A rs755170084 0.00001
NM_022489.4(INF2):c.*358C>T rs1312922081 0.00001
NM_022489.4(INF2):c.*815C>T rs886050385 0.00001
NM_022489.4(INF2):c.1777G>A (p.Glu593Lys) rs775320095 0.00001
NM_022489.4(INF2):c.2389C>T (p.Arg797Cys) rs941477086 0.00001
NM_022489.4(INF2):c.2415G>A (p.Leu805=) rs779751728 0.00001
NM_022489.4(INF2):c.2701G>A (p.Ala901Thr) rs775349897 0.00001
NM_022489.4(INF2):c.2908G>A (p.Val970Met) rs977752085 0.00001
NM_022489.4(INF2):c.2987C>T (p.Thr996Ile) rs377414980 0.00001
NM_022489.4(INF2):c.3190T>C (p.Leu1064=) rs886050383 0.00001
NM_022489.4(INF2):c.3418G>A (p.Val1140Ile) rs199640596 0.00001
NM_022489.4(INF2):c.409G>A (p.Val137Met) rs200713451 0.00001
NM_022489.4(INF2):c.641G>A (p.Arg214His) rs267606879 0.00001
NM_022489.4(INF2):c.986-14A>G rs774186716 0.00001
NM_022489.4(INF2):c.*187C>T rs1056002023
NM_022489.4(INF2):c.*25A>G rs541048885
NM_022489.4(INF2):c.*396G>T rs1890456253
NM_022489.4(INF2):c.*503C>T rs1890461695
NM_022489.4(INF2):c.1103A>G (p.Gln368Arg) rs1481694989
NM_022489.4(INF2):c.1126A>T (p.Thr376Ser) rs376942822
NM_022489.4(INF2):c.125T>C (p.Leu42Pro) rs267606880
NM_022489.4(INF2):c.1275A>C (p.Pro425=) rs760828390
NM_022489.4(INF2):c.144C>T (p.Val48=) rs528508846
NM_022489.4(INF2):c.1575C>T (p.Thr525=) rs1417311904
NM_022489.4(INF2):c.1582C>T (p.Pro528Ser) rs181694819
NM_022489.4(INF2):c.161G>C (p.Arg54Pro) rs866348422
NM_022489.4(INF2):c.167G>A (p.Arg56His) rs1595163730
NM_022489.4(INF2):c.2009A>G (p.Glu670Gly) rs886050381
NM_022489.4(INF2):c.2022A>T (p.Gln674His) rs886050382
NM_022489.4(INF2):c.217G>A (p.Gly73Ser) rs1566777560
NM_022489.4(INF2):c.2507T>C (p.Ile836Thr) rs767351070
NM_022489.4(INF2):c.2517G>A (p.Glu839=) rs561061092
NM_022489.4(INF2):c.254C>G (p.Ser85Trp) rs1317776692
NM_022489.4(INF2):c.2709G>C (p.Gln903His) rs762803590
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.3361C>G (p.Pro1121Ala) rs1248997686
NM_022489.4(INF2):c.3446G>C (p.Ser1149Thr) rs1890205619
NM_022489.4(INF2):c.353T>A (p.Ile118Asn) rs2140639518
NM_022489.4(INF2):c.3740_3741del (p.Val1247fs) rs753327806
NM_022489.4(INF2):c.391+6C>T rs75115369
NM_022489.4(INF2):c.459C>G (p.Tyr153Ter) rs754706068
NM_022489.4(INF2):c.485T>C (p.Leu162Pro) rs2140647298
NM_022489.4(INF2):c.529C>T (p.Arg177Cys) rs1595166085
NM_022489.4(INF2):c.530G>A (p.Arg177His) rs1566778651
NM_022489.4(INF2):c.550G>A (p.Glu184Lys) rs1566778676
NM_022489.4(INF2):c.556T>C (p.Ser186Pro) rs267606877
NM_022489.4(INF2):c.604A>G (p.Asn202Asp)
NM_022489.4(INF2):c.605A>G (p.Asn202Ser) rs2140648522
NM_022489.4(INF2):c.607G>A (p.Ala203Thr) rs1213058223
NM_022489.4(INF2):c.625G>A (p.Glu209Lys) rs1012899025
NM_022489.4(INF2):c.640C>T (p.Arg214Cys) rs912928648
NM_022489.4(INF2):c.652C>T (p.Arg218Trp) rs267606878
NM_022489.4(INF2):c.653G>A (p.Arg218Gln) rs267607183
NM_022489.4(INF2):c.658G>A (p.Glu220Lys) rs530391015
NM_022489.4(INF2):c.739G>C (p.Ala247Pro) rs991189454

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