ClinVar Miner

List of variants in gene INF2 reported as uncertain significance by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 42
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HGVS dbSNP gnomAD frequency
NM_022489.4(INF2):c.*803G>A rs555692643 0.00041
NM_022489.4(INF2):c.966C>T (p.Ala322=) rs774024906 0.00013
NM_022489.4(INF2):c.1197C>T (p.His399=) rs746493706 0.00009
NM_022489.4(INF2):c.3654C>T (p.Thr1218=) rs557462297 0.00009
NM_022489.4(INF2):c.597C>T (p.Ser199=) rs372269719 0.00007
NM_022489.4(INF2):c.*447A>T rs749782054 0.00006
NM_022489.4(INF2):c.1448C>T (p.Ser483Phe) rs753188664 0.00006
NM_022489.4(INF2):c.*311T>A rs975205957 0.00005
NM_022489.4(INF2):c.2440G>A (p.Asp814Asn) rs373532334 0.00005
NM_022489.4(INF2):c.*314G>A rs921070326 0.00003
NM_022489.4(INF2):c.2201T>G (p.Val734Gly) rs754128624 0.00003
NM_022489.4(INF2):c.2847G>A (p.Ala949=) rs754546219 0.00003
NM_022489.4(INF2):c.18C>T (p.Gly6=) rs1032255653 0.00002
NM_022489.4(INF2):c.2775+13G>A rs759589756 0.00002
NM_022489.4(INF2):c.3703C>T (p.Pro1235Ser) rs201091360 0.00002
NM_022489.4(INF2):c.*153C>T rs899450753 0.00001
NM_022489.4(INF2):c.*232G>A rs886050384 0.00001
NM_022489.4(INF2):c.*289G>A rs755170084 0.00001
NM_022489.4(INF2):c.*358C>T rs1312922081 0.00001
NM_022489.4(INF2):c.*815C>T rs886050385 0.00001
NM_022489.4(INF2):c.1777G>A (p.Glu593Lys) rs775320095 0.00001
NM_022489.4(INF2):c.2389C>T (p.Arg797Cys) rs941477086 0.00001
NM_022489.4(INF2):c.2415G>A (p.Leu805=) rs779751728 0.00001
NM_022489.4(INF2):c.2701G>A (p.Ala901Thr) rs775349897 0.00001
NM_022489.4(INF2):c.2987C>T (p.Thr996Ile) rs377414980 0.00001
NM_022489.4(INF2):c.3190T>C (p.Leu1064=) rs886050383 0.00001
NM_022489.4(INF2):c.986-14A>G rs774186716 0.00001
NM_022489.4(INF2):c.*187C>T rs1056002023
NM_022489.4(INF2):c.*396G>T rs1890456253
NM_022489.4(INF2):c.*503C>T rs1890461695
NM_022489.4(INF2):c.1103A>G (p.Gln368Arg) rs1481694989
NM_022489.4(INF2):c.1126A>T (p.Thr376Ser) rs376942822
NM_022489.4(INF2):c.1262CACCCC[3] (p.Pro427_Pro428del) rs573567814
NM_022489.4(INF2):c.1575C>T (p.Thr525=) rs1417311904
NM_022489.4(INF2):c.2009A>G (p.Glu670Gly) rs886050381
NM_022489.4(INF2):c.2022A>T (p.Gln674His) rs886050382
NM_022489.4(INF2):c.2709G>C (p.Gln903His) rs762803590
NM_022489.4(INF2):c.2845G>A (p.Ala949Thr) rs2140695225
NM_022489.4(INF2):c.3361C>G (p.Pro1121Ala) rs1248997686
NM_022489.4(INF2):c.3446G>C (p.Ser1149Thr) rs1890205619
NM_022489.4(INF2):c.459C>G (p.Tyr153Ter) rs754706068
NM_022489.4(INF2):c.625G>A (p.Glu209Lys) rs1012899025

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