ClinVar Miner

List of variants reported as benign for Inflammatory bowel disease 28

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Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_001558.4(IL10RA):c.1051A>G (p.Arg351Gly) rs2229113 0.73756
NM_001558.4(IL10RA):c.*1730G>A rs9610 0.52512
NM_001558.4(IL10RA):c.459A>G (p.Ala153=) rs2256111 0.50461
NM_001558.4(IL10RA):c.180G>A (p.Ala60=) rs4252249 0.12518
NM_001558.4(IL10RA):c.475A>G (p.Ser159Gly) rs3135932 0.11335
NM_001558.4(IL10RA):c.525G>A (p.Pro175=) rs2228054 0.04875
NM_001558.4(IL10RA):c.670A>G (p.Ile224Val) rs2228055 0.04765
NM_001558.4(IL10RA):c.972C>T (p.Thr324=) rs2229115 0.03477
NM_001558.4(IL10RA):c.1259C>T (p.Ser420Leu) rs2229114 0.03293
NM_001558.4(IL10RA):c.*1412T>C rs4252294 0.02065
NM_001558.4(IL10RA):c.181C>G (p.Leu61Val) rs4252250 0.01376
NM_001558.4(IL10RA):c.*354T>C rs4252292 0.01359
NM_001558.4(IL10RA):c.*1348G>C rs4252293 0.01357
NM_001558.4(IL10RA):c.337G>A (p.Val113Ile) rs4252303 0.00655
NM_001558.4(IL10RA):c.312C>T (p.Asp104=) rs35511069 0.00653
NM_001558.4(IL10RA):c.21G>C (p.Val7=) rs4252301 0.00575
NM_001558.4(IL10RA):c.697G>A (p.Val233Met) rs41354146 0.00459
NM_001558.4(IL10RA):c.1188G>A (p.Arg396=) rs35465632 0.00388
NM_001558.4(IL10RA):c.75G>T (p.Glu25Asp) rs150140303 0.00324
NM_001558.4(IL10RA):c.67+8T>C rs200992970 0.00290
NM_001558.4(IL10RA):c.136A>G (p.Thr46Ala) rs112317511 0.00277
NM_001558.4(IL10RA):c.696C>T (p.Thr232=) rs4252311 0.00274
NM_001558.4(IL10RA):c.1158C>G (p.Thr386=) rs4252290 0.00180
NM_001558.4(IL10RA):c.144C>T (p.Ile48=) rs140466541 0.00178
NM_001558.4(IL10RA):c.1041G>A (p.Thr347=) rs62636561 0.00156
NC_000011.10:g.117986053G>T rs867553241 0.00093
NM_001558.4(IL10RA):c.810+10G>A rs12290349 0.00092
NM_001558.4(IL10RA):c.1401G>A (p.Ser467=) rs150551465 0.00076
NM_001558.4(IL10RA):c.1638C>T (p.Ala546=) rs146193205 0.00073
NM_001558.4(IL10RA):c.68-16A>G rs546258420 0.00031
NM_001558.4(IL10RA):c.931T>C (p.Leu311=) rs148808529 0.00011
NM_001558.4(IL10RA):c.1360G>A (p.Glu454Lys) rs79887053 0.00007
NM_001558.4(IL10RA):c.336C>T (p.Thr112=) rs192749274 0.00007
NM_001558.4(IL10RA):c.*968G>A rs562515149 0.00005
NM_001558.4(IL10RA):c.72A>C (p.Thr24=) rs560128585 0.00002
NM_001558.4(IL10RA):c.716T>C (p.Phe239Ser) rs541386535 0.00001
NM_001558.4(IL10RA):c.368-18C>A rs4252308
NM_001558.4(IL10RA):c.368-18C>G rs4252308
NM_001558.4(IL10RA):c.67+11G>C rs376956484

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