ClinVar Miner

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

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Gene type:
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Total variants: 37
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HGVS dbSNP
NM_022489.4(INF2):c.1+171A>G rs4247030
NM_022489.4(INF2):c.1+174C>T rs4247031
NM_022489.4(INF2):c.1+185C>T rs74395064
NM_022489.4(INF2):c.1262_1267CACCCC[2] (p.Pro425_Pro428del) rs573567814
NM_022489.4(INF2):c.1582C>T (p.Pro528Ser) rs181694819
NM_022489.4(INF2):c.1736-175C>T rs113514625
NM_022489.4(INF2):c.1736-51G>A rs117034570
NM_022489.4(INF2):c.1950-231C>T rs73345596
NM_022489.4(INF2):c.2239+256G>A rs12882277
NM_022489.4(INF2):c.2310+8del rs3840006
NM_022489.4(INF2):c.2322C>T (p.Thr774=) rs59751492
NM_022489.4(INF2):c.2489+117C>T rs4983533
NM_022489.4(INF2):c.2489+53T>C rs4983531
NM_022489.4(INF2):c.2489+62G>C rs4983532
NM_022489.4(INF2):c.2490-292T>C rs4983534
NM_022489.4(INF2):c.2611-122G>C rs4497619
NM_022489.4(INF2):c.2611-84G>A rs10144190
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.3041-146C>G rs118061751
NM_022489.4(INF2):c.3041-56C>T rs9672043
NM_022489.4(INF2):c.3041-75G>A rs13379430
NM_022489.4(INF2):c.3066T>C (p.Asp1022=) rs4983535
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>G (p.Pro1069=) rs1128840
NM_022489.4(INF2):c.3244G>T (p.Ala1082Ser) rs143540449
NM_022489.4(INF2):c.3478G>A (p.Gly1160Ser) rs9672065
NM_022489.4(INF2):c.3684G>A (p.Arg1228=) rs189263181
NM_022489.4(INF2):c.3747G>A (p.Gln1249=) rs149939482
NM_022489.4(INF2):c.391+321C>T rs11160817
NM_022489.4(INF2):c.391+6C>T rs75115369
NM_022489.4(INF2):c.42G>A (p.Leu14=) rs62638758
NM_022489.4(INF2):c.668-32C>T rs7145566
NM_022489.4(INF2):c.702-57G>A rs79559717
NM_022489.4(INF2):c.879G>A (p.Ser293=) rs184709736
NM_022489.4(INF2):c.985+66G>A rs57402537

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