ClinVar Miner

List of variants in gene INF2 studied for not specified

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Gene type:
ClinVar version:
Total variants: 100
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HGVS dbSNP
NM_022489.4(INF2):c.*10C>T rs142710295
NM_022489.4(INF2):c.-10+16C>A rs77549829
NM_022489.4(INF2):c.-10G>A rs115602636
NM_022489.4(INF2):c.-10G>C rs115602636
NM_022489.4(INF2):c.1+1G>C rs758452999
NM_022489.4(INF2):c.1049C>T (p.Pro350Leu) rs146529868
NM_022489.4(INF2):c.105C>T (p.Pro35=) rs4983530
NM_022489.4(INF2):c.1078G>A (p.Val360Ile) rs114820975
NM_022489.4(INF2):c.1115C>T (p.Ser372Phe) rs770882784
NM_022489.4(INF2):c.1189G>A (p.Val397Met) rs771775245
NM_022489.4(INF2):c.1227G>T (p.Ser409=) rs3809455
NM_022489.4(INF2):c.1262_1267CACCCC[2] (p.Pro425_Pro428del) rs573567814
NM_022489.4(INF2):c.1262_1267CACCCC[3] (p.Pro427_Pro428del) rs573567814
NM_022489.4(INF2):c.1281_1286del (p.Pro428_Leu429del) rs751555478
NM_022489.4(INF2):c.1372C>T (p.Pro458Ser) rs760986113
NM_022489.4(INF2):c.1448C>T (p.Ser483Phe) rs753188664
NM_022489.4(INF2):c.1451G>A (p.Cys484Tyr) rs201323100
NM_022489.4(INF2):c.1452T>C (p.Cys484=) rs371775604
NM_022489.4(INF2):c.1499C>T (p.Pro500Leu) rs561201601
NM_022489.4(INF2):c.1503C>T (p.Pro501=) rs1057520913
NM_022489.4(INF2):c.1547C>T (p.Pro516Leu) rs111589086
NM_022489.4(INF2):c.1582C>T (p.Pro528Ser) rs181694819
NM_022489.4(INF2):c.1614C>T (p.Ile538=) rs201561899
NM_022489.4(INF2):c.1736-18C>T rs199612826
NM_022489.4(INF2):c.1736-6C>T rs371991103
NM_022489.4(INF2):c.1755G>A (p.Ala585=) rs375573206
NM_022489.4(INF2):c.1771G>A (p.Asp591Asn) rs369421697
NM_022489.4(INF2):c.1773C>T (p.Asp591=) rs201853087
NM_022489.4(INF2):c.1791C>T (p.Pro597=) rs377222356
NM_022489.4(INF2):c.1887+8C>T rs569295413
NM_022489.4(INF2):c.1949+16A>G rs11850821
NM_022489.4(INF2):c.1950-10C>T rs199987321
NM_022489.4(INF2):c.1950-4C>G rs539363877
NM_022489.4(INF2):c.1978C>T (p.Arg660Trp) rs138577569
NM_022489.4(INF2):c.2019_2022del (p.Lys673fs) rs1060499868
NM_022489.4(INF2):c.2052+12A>G rs1342540362
NM_022489.4(INF2):c.2053A>G (p.Ile685Val) rs199526439
NM_022489.4(INF2):c.2138+12C>T rs186410473
NM_022489.4(INF2):c.2139-11G>A rs1057523138
NM_022489.4(INF2):c.2240-5T>C rs765264633
NM_022489.4(INF2):c.2310+8del rs3840006
NM_022489.4(INF2):c.2322C>T (p.Thr774=) rs59751492
NM_022489.4(INF2):c.2331C>A (p.Ala777=) rs1293312025
NM_022489.4(INF2):c.2418+19G>A rs770701500
NM_022489.4(INF2):c.2419-14G>A rs746955943
NM_022489.4(INF2):c.2433C>T (p.Ser811=) rs140010249
NM_022489.4(INF2):c.2458C>T (p.Arg820Trp) rs79327775
NM_022489.4(INF2):c.2490-20C>T rs187104422
NM_022489.4(INF2):c.2571C>T (p.Ser857=) rs62640005
NM_022489.4(INF2):c.2598C>T (p.Thr866=) rs552110857
NM_022489.4(INF2):c.2611-12C>T rs1057522725
NM_022489.4(INF2):c.2630G>A (p.Arg877Gln) rs142678449
NM_022489.4(INF2):c.2640T>C (p.Asp880=) rs10133301
NM_022489.4(INF2):c.2683G>A (p.Asp895Asn) rs776314008
NM_022489.4(INF2):c.2766C>T (p.Arg922=) rs201044782
NM_022489.4(INF2):c.2775+15C>T rs73347508
NM_022489.4(INF2):c.2875C>T (p.Pro959Ser) rs369417066
NM_022489.4(INF2):c.2885A>C (p.Lys962Thr) rs376067427
NM_022489.4(INF2):c.2991C>T (p.Asp997=) rs1057523828
NM_022489.4(INF2):c.2999G>A (p.Ser1000Asn) rs148541427
NM_022489.4(INF2):c.3032C>G (p.Thr1011Arg) rs551015347
NM_022489.4(INF2):c.3040+11C>T rs374390500
NM_022489.4(INF2):c.3040+16A>G rs367565825
NM_022489.4(INF2):c.3066T>C (p.Asp1022=) rs4983535
NM_022489.4(INF2):c.3069C>T (p.Pro1023=) rs75382114
NM_022489.4(INF2):c.3078C>T (p.Ser1026=) rs377023270
NM_022489.4(INF2):c.3080C>T (p.Thr1027Met) rs760488958
NM_022489.4(INF2):c.3103G>A (p.Gly1035Ser) rs368995122
NM_022489.4(INF2):c.3108T>C (p.Leu1036=) rs186075307
NM_022489.4(INF2):c.3153C>T (p.Asp1051=) rs117457867
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.3221G>A (p.Arg1074Lys) rs201445955
NM_022489.4(INF2):c.3286C>T (p.Pro1096Ser) rs34251364
NM_022489.4(INF2):c.3404C>T (p.Thr1135Met) rs3803311
NM_022489.4(INF2):c.3476G>A (p.Arg1159His) rs200591522
NM_022489.4(INF2):c.3478G>A (p.Gly1160Ser) rs9672065
NM_022489.4(INF2):c.3563C>T (p.Ser1188Phe) rs201715539
NM_022489.4(INF2):c.3638G>A (p.Arg1213Gln) rs199801767
NM_022489.4(INF2):c.3694+16G>A rs556924432
NM_022489.4(INF2):c.3747G>A (p.Gln1249=) rs149939482
NM_022489.4(INF2):c.37G>A (p.Ala13Thr) rs201383094
NM_022489.4(INF2):c.391+17G>A rs4074531
NM_022489.4(INF2):c.391+18A>T rs115458897
NM_022489.4(INF2):c.391+6C>T rs75115369
NM_022489.4(INF2):c.42G>A (p.Leu14=) rs62638758
NM_022489.4(INF2):c.489C>T (p.Asp163=) rs769080446
NM_022489.4(INF2):c.507+7G>A rs201568246
NM_022489.4(INF2):c.508-13G>A rs764942605
NM_022489.4(INF2):c.519C>T (p.Ser173=) rs780247558
NM_022489.4(INF2):c.549C>T (p.Asn183=) rs1555373624
NM_022489.4(INF2):c.624C>T (p.Pro208=) rs750610272
NM_022489.4(INF2):c.668-12G>A rs367924307
NM_022489.4(INF2):c.701+19G>A rs371962265
NM_022489.4(INF2):c.782G>A (p.Arg261Gln) rs749543418
NM_022489.4(INF2):c.798C>G (p.Val266=) rs375005967
NM_022489.4(INF2):c.843+16C>T rs118017785
NM_022489.4(INF2):c.879G>A (p.Ser293=) rs184709736
NM_022489.4(INF2):c.973C>T (p.Leu325=) rs1057521829
NM_022489.4(INF2):c.985+10C>T rs755849718

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