ClinVar Miner

List of variants in gene INF2 reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 36
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HGVS dbSNP gnomAD frequency
NM_022489.4(INF2):c.2440G>A (p.Asp814Asn) rs373532334 0.00005
NM_022489.4(INF2):c.1147G>A (p.Val383Met) rs780689756 0.00004
NM_022489.4(INF2):c.1183G>A (p.Glu395Lys) rs374769850 0.00004
NM_022489.4(INF2):c.3611C>T (p.Ser1204Leu) rs376222605 0.00004
NM_022489.4(INF2):c.1316C>T (p.Pro439Leu) rs1375222598 0.00002
NM_022489.4(INF2):c.2005G>A (p.Val669Met) rs756038490 0.00002
NM_022489.4(INF2):c.1189G>A (p.Val397Met) rs771775245 0.00001
NM_022489.4(INF2):c.2767G>A (p.Ala923Thr) rs774099930 0.00001
NM_022489.4(INF2):c.2879-20G>C rs879254306 0.00001
NM_022489.4(INF2):c.2897A>G (p.Lys966Arg) rs879254296 0.00001
NM_022489.4(INF2):c.3356A>C (p.Asn1119Thr) rs200246759 0.00001
NM_022489.4(INF2):c.3494C>T (p.Ala1165Val) rs771044828 0.00001
NM_022489.4(INF2):c.3523G>A (p.Asp1175Asn) rs765901404 0.00001
NM_022489.4(INF2):c.3535A>G (p.Thr1179Ala) rs778879482 0.00001
NM_022489.4(INF2):c.1183G>C (p.Glu395Gln) rs374769850
NM_022489.4(INF2):c.1288C>T (p.Leu430Phe) rs1131691501
NM_022489.4(INF2):c.1589del (p.Val530fs) rs879254321
NM_022489.4(INF2):c.1666C>T (p.Arg556Trp) rs879254313
NM_022489.4(INF2):c.1774G>A (p.Ala592Thr) rs530285485
NM_022489.4(INF2):c.1810C>T (p.Arg604Ter) rs1260381635
NM_022489.4(INF2):c.2080G>A (p.Glu694Lys)
NM_022489.4(INF2):c.25C>A (p.Arg9Ser) rs1889485557
NM_022489.4(INF2):c.2726C>A (p.Thr909Lys) rs201336550
NM_022489.4(INF2):c.2726C>T (p.Thr909Met) rs201336550
NM_022489.4(INF2):c.2858G>A (p.Arg953Gln) rs1385146569
NM_022489.4(INF2):c.2875C>T (p.Pro959Ser) rs369417066
NM_022489.4(INF2):c.3206_3207inv (p.Pro1069Leu)
NM_022489.4(INF2):c.3257T>C (p.Leu1086Pro) rs368869709
NM_022489.4(INF2):c.3406T>A (p.Ser1136Thr)
NM_022489.4(INF2):c.3427G>A (p.Ala1143Thr)
NM_022489.4(INF2):c.3513_3518del (p.1171DE[2])
NM_022489.4(INF2):c.3583G>C (p.Glu1195Gln) rs1064796974
NM_022489.4(INF2):c.3740_3741del (p.Val1247fs) rs753327806
NM_022489.4(INF2):c.397G>A (p.Asp133Asn) rs774135330
NM_022489.4(INF2):c.829T>C (p.Ser277Pro)
NM_022489.4(INF2):c.878C>T (p.Ser293Leu)

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