ClinVar Miner

List of variants in gene INF2 reported by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 74
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HGVS dbSNP
NM_022489.3(INF2):c.*10C>T rs142710295
NM_022489.3(INF2):c.*136C>T rs150579444
NM_022489.3(INF2):c.*16C>T rs199912466
NM_022489.3(INF2):c.*232G>A rs886050384
NM_022489.3(INF2):c.*25A>G rs541048885
NM_022489.3(INF2):c.*288C>T rs534561202
NM_022489.3(INF2):c.*388A>G rs140513391
NM_022489.3(INF2):c.*437G>A rs1128866
NM_022489.3(INF2):c.*536G>T rs1128880
NM_022489.3(INF2):c.*544G>A rs111978619
NM_022489.3(INF2):c.*815C>T rs886050385
NM_022489.3(INF2):c.-10G>A rs115602636
NM_022489.3(INF2):c.-50G>A rs886050379
NM_022489.3(INF2):c.-85G>A rs141884370
NM_022489.3(INF2):c.1049C>T (p.Pro350Leu) rs146529868
NM_022489.3(INF2):c.105C>T (p.Pro35=) rs4983530
NM_022489.3(INF2):c.1078G>A (p.Val360Ile) rs114820975
NM_022489.3(INF2):c.1126A>T (p.Thr376Ser) rs376942822
NM_022489.3(INF2):c.1144A>G (p.Ser382Gly) rs201077878
NM_022489.3(INF2):c.1197C>T (p.His399=) rs746493706
NM_022489.3(INF2):c.1227G>T (p.Ser409=) rs3809455
NM_022489.3(INF2):c.1280_1285delCACCCC (p.Pro427_Pro428del) rs573567814
NM_022489.3(INF2):c.1360C>T (p.Leu454Phe) rs545495465
NM_022489.3(INF2):c.144C>T (p.Val48=) rs528508846
NM_022489.3(INF2):c.1451G>A (p.Cys484Tyr) rs201323100
NM_022489.3(INF2):c.1582C>T (p.Pro528Ser) rs181694819
NM_022489.3(INF2):c.1587C>T (p.Pro529=) rs755649066
NM_022489.3(INF2):c.1647A>G (p.Ala549=) rs201674759
NM_022489.3(INF2):c.1755G>A (p.Ala585=) rs375573206
NM_022489.3(INF2):c.1770C>T (p.Pro590=) rs549506051
NM_022489.3(INF2):c.1777G>A (p.Glu593Lys) rs775320095
NM_022489.3(INF2):c.1806C>T (p.Ile602=) rs760506368
NM_022489.3(INF2):c.1865G>A (p.Arg622Gln) rs200155666
NM_022489.3(INF2):c.1978C>T (p.Arg660Trp) rs138577569
NM_022489.3(INF2):c.2009A>G (p.Glu670Gly) rs886050381
NM_022489.3(INF2):c.2022A>T (p.Gln674His) rs886050382
NM_022489.3(INF2):c.2053A>G (p.Ile685Val) rs199526439
NM_022489.3(INF2):c.2201T>G (p.Val734Gly) rs754128624
NM_022489.3(INF2):c.2310+8delA rs3840006
NM_022489.3(INF2):c.2322C>T (p.Thr774=) rs59751492
NM_022489.3(INF2):c.2458C>T (p.Arg820Trp) rs79327775
NM_022489.3(INF2):c.2517G>A (p.Glu839=) rs561061092
NM_022489.3(INF2):c.2571C>T (p.Ser857=) rs62640005
NM_022489.3(INF2):c.2630G>A (p.Arg877Gln) rs142678449
NM_022489.3(INF2):c.2640T>C (p.Asp880=) rs10133301
NM_022489.3(INF2):c.2775+15C>T rs73347508
NM_022489.3(INF2):c.2848C>T (p.Arg950Trp) rs199873407
NM_022489.3(INF2):c.2987C>T (p.Thr996Ile) rs377414980
NM_022489.3(INF2):c.3066T>C (p.Asp1022=) rs4983535
NM_022489.3(INF2):c.3069C>T (p.Pro1023=) rs75382114
NM_022489.3(INF2):c.3078C>T (p.Ser1026=) rs377023270
NM_022489.3(INF2):c.3108T>C (p.Leu1036=) rs186075307
NM_022489.3(INF2):c.3134G>A (p.Arg1045Gln) rs200369827
NM_022489.3(INF2):c.3153C>T (p.Asp1051=) rs117457867
NM_022489.3(INF2):c.3190T>C (p.Leu1064=) rs886050383
NM_022489.3(INF2):c.3206C>T (p.Pro1069Leu) rs376139171
NM_022489.3(INF2):c.3207A>C (p.Pro1069=) rs1128840
NM_022489.3(INF2):c.3207A>G (p.Pro1069=) rs1128840
NM_022489.3(INF2):c.3221G>A (p.Arg1074Lys) rs201445955
NM_022489.3(INF2):c.3286C>T (p.Pro1096Ser) rs34251364
NM_022489.3(INF2):c.3404C>T (p.Thr1135Met) rs3803311
NM_022489.3(INF2):c.3478G>A (p.Gly1160Ser) rs9672065
NM_022489.3(INF2):c.3550G>A (p.Ala1184Thr) rs374684004
NM_022489.3(INF2):c.3563C>T (p.Ser1188Phe) rs201715539
NM_022489.3(INF2):c.3684G>A (p.Arg1228=) rs189263181
NM_022489.3(INF2):c.37G>A (p.Ala13Thr) rs201383094
NM_022489.3(INF2):c.391+6C>T rs75115369
NM_022489.3(INF2):c.42G>A (p.Leu14=) rs62638758
NM_022489.3(INF2):c.459C>G (p.Tyr153Ter)
NM_022489.3(INF2):c.507+7G>A rs201568246
NM_022489.3(INF2):c.879G>A (p.Ser293=) rs184709736
NM_022489.3(INF2):c.885G>A (p.Leu295=) rs370680236
NM_022489.3(INF2):c.966C>T (p.Ala322=) rs774024906
NM_022489.3(INF2):c.986-14A>G rs774186716

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