ClinVar Miner

List of variants in gene INF2 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 60
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HGVS dbSNP
NM_022489.4(INF2):c.-10+16C>A rs77549829
NM_022489.4(INF2):c.-10G>C rs115602636
NM_022489.4(INF2):c.1115C>T (p.Ser372Phe) rs770882784
NM_022489.4(INF2):c.1197C>T (p.His399=) rs746493706
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.1499C>T (p.Pro500Leu) rs561201601
NM_022489.4(INF2):c.1503C>T (p.Pro501=) rs1057520913
NM_022489.4(INF2):c.1614C>T (p.Ile538=) rs201561899
NM_022489.4(INF2):c.1735+73G>A
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.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.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.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.2239+165C>T
NM_022489.4(INF2):c.2240-5T>C rs765264633
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.2458C>T (p.Arg820Trp) rs79327775
NM_022489.4(INF2):c.2490-20C>T rs187104422
NM_022489.4(INF2):c.2550C>T (p.Thr850=) rs771112980
NM_022489.4(INF2):c.2598C>T (p.Thr866=) rs552110857
NM_022489.4(INF2):c.2611-12C>T rs1057522725
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.2991C>T (p.Asp997=) rs1057523828
NM_022489.4(INF2):c.2999G>A (p.Ser1000Asn) rs148541427
NM_022489.4(INF2):c.3040+11C>T rs374390500
NM_022489.4(INF2):c.3040+16A>G rs367565825
NM_022489.4(INF2):c.3103G>A (p.Gly1035Ser) rs368995122
NM_022489.4(INF2):c.3134G>A (p.Arg1045Gln) rs200369827
NM_022489.4(INF2):c.3221G>A (p.Arg1074Lys) rs201445955
NM_022489.4(INF2):c.3476G>A (p.Arg1159His) rs200591522
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.37G>A (p.Ala13Thr) rs201383094
NM_022489.4(INF2):c.507+7G>A rs201568246
NM_022489.4(INF2):c.508-13G>A rs764942605
NM_022489.4(INF2):c.510G>A (p.Thr170=)
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.558C>T (p.Ser186=) rs150714865
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.844-252T>C
NM_022489.4(INF2):c.973C>T (p.Leu325=) rs1057521829
NM_022489.4(INF2):c.985+10C>T rs755849718

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