ClinVar Miner

List of variants reported as benign for Focal segmental glomerulosclerosis 5

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Total variants: 71
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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.-85G>A rs141884370 0.09252
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.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.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.3221G>A (p.Arg1074Lys) rs201445955 0.00036
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.3684G>A (p.Arg1228=) rs189263181 0.00014
NM_022489.4(INF2):c.1755G>A (p.Ala585=) rs375573206 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.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.1499C>T (p.Pro500Leu) rs561201601 0.00009
NM_022489.4(INF2):c.1806C>T (p.Ile602=) rs760506368 0.00009
NM_022489.4(INF2):c.*1+1G>C rs758452999 0.00007
NM_022489.4(INF2):c.1587C>T (p.Pro529=) rs755649066 0.00005
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.*25A>G rs541048885
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.1582C>T (p.Pro528Ser) rs181694819
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.3207A>C (p.Pro1069=) rs1128840
NM_022489.4(INF2):c.3207A>G (p.Pro1069=) rs1128840
NM_022489.4(INF2):c.391+6C>T rs75115369

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