ClinVar Miner

List of variants in gene NOD2 studied for Sarcoidosis, early-onset

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Total variants: 80
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HGVS dbSNP
NM_022162.3(NOD2):c.*9G>A rs104895459
NM_022162.3(NOD2):c.1000C>T (p.Arg334Trp) rs104895462
NM_022162.3(NOD2):c.1001G>A (p.Arg334Gln) rs104895461
NM_022162.3(NOD2):c.1042C>G (p.Leu348Val) rs104895428
NM_022162.3(NOD2):c.1065G>A (p.Trp355Ter) rs104895488
NM_022162.3(NOD2):c.1070A>C (p.Asp357Ala) rs104895469
NM_022162.3(NOD2):c.1087A>T (p.Ile363Phe) rs104895470
NM_022162.3(NOD2):c.1117C>T (p.Arg373Cys) rs145293873
NM_022162.3(NOD2):c.113G>T (p.Arg38Met) rs104895487
NM_022162.3(NOD2):c.1146C>G (p.Asp382Glu) rs104895476
NM_022162.3(NOD2):c.1147G>A (p.Glu383Lys) rs104895477
NM_022162.3(NOD2):c.1148A>G (p.Glu383Gly) rs104895493
NM_022162.3(NOD2):c.1171C>T (p.Arg391Cys) rs104895481
NM_022162.3(NOD2):c.1241A>G (p.Asn414Ser) rs104895429
NM_022162.3(NOD2):c.1281G>A (p.Pro427=) rs104895430
NM_022162.3(NOD2):c.1292C>T (p.Ser431Leu) rs104895431
NM_022162.3(NOD2):c.1321G>A (p.Glu441Lys) rs104895432
NM_022162.3(NOD2):c.1366C>T (p.Leu456=) rs104895433
NM_022162.3(NOD2):c.1387C>G (p.Pro463Ala) rs104895482
NM_022162.3(NOD2):c.1390G>T (p.Gly464Trp) rs104895492
NM_022162.3(NOD2):c.1405C>T (p.Leu469Phe) rs104895460
NM_022162.3(NOD2):c.1442G>A (p.Gly481Asp) rs104895494
NM_022162.3(NOD2):c.1469G>T (p.Trp490Leu) rs104895480
NM_022162.3(NOD2):c.1484G>A (p.Cys495Tyr) rs104895478
NM_022162.3(NOD2):c.1487A>T (p.His496Leu) rs104895472
NM_022162.3(NOD2):c.1509G>A (p.Glu503=) rs104895434
NM_022162.3(NOD2):c.1538T>C (p.Met513Thr) rs104895473
NM_022162.3(NOD2):c.1581C>G (p.Pro527=) rs104895435
NM_022162.3(NOD2):c.1648C>G (p.Leu550Val) rs104895471
NM_022162.3(NOD2):c.1672_1677del (p.Leu558_Gly559del) rs104895436
NM_022162.3(NOD2):c.1759C>T (p.Arg587Cys) rs104895479
NM_022162.3(NOD2):c.1788G>A (p.Thr596=) rs104895437
NM_022162.3(NOD2):c.1813A>C (p.Thr605Pro) rs104895474
NM_022162.3(NOD2):c.1834G>A (p.Ala612Thr) rs104895438
NM_022162.3(NOD2):c.1835C>T (p.Ala612Val) rs104895439
NM_022162.3(NOD2):c.2010C>A (p.Asn670Lys) rs104895475
NM_022162.3(NOD2):c.2137C>T (p.Arg713Cys) rs104895440
NM_022162.3(NOD2):c.2138G>A (p.Arg713His) rs104895483
NM_022162.3(NOD2):c.2180C>T (p.Pro727Leu) rs104895489
NM_022162.3(NOD2):c.2220C>T (p.Ile740=) rs104895441
NM_022162.3(NOD2):c.2273C>T (p.Ala758Val) rs104895442
NM_022162.3(NOD2):c.2332G>A (p.Glu778Lys) rs104895443
NM_022162.3(NOD2):c.2371C>T (p.Arg791Trp) rs104895484
NM_022162.3(NOD2):c.2372G>A (p.Arg791Gln) rs104895464
NM_022162.3(NOD2):c.2377G>A (p.Val793Met) rs104895444
NM_022162.3(NOD2):c.2406G>T (p.Val802=) rs104895495
NM_022162.3(NOD2):c.2475C>G (p.Asn825Lys) rs104895485
NM_022162.3(NOD2):c.2527G>A (p.Glu843Lys) rs104895445
NM_022162.3(NOD2):c.2546C>T (p.Ala849Val) rs104895486
NM_022162.3(NOD2):c.2555A>G (p.Asn852Ser) rs104895467
NM_022162.3(NOD2):c.2558A>G (p.Asn853Ser) rs104895446
NM_022162.3(NOD2):c.2587A>G (p.Met863Val) rs104895447
NM_022162.3(NOD2):c.2619C>T (p.Phe873=) rs104895448
NM_022162.3(NOD2):c.2630+35T>A rs104895449
NM_022162.3(NOD2):c.2631-5T>C rs104895450
NM_022162.3(NOD2):c.2715-75G>A rs104895466
NM_022162.3(NOD2):c.2715-81G>A rs104895465
NM_022162.3(NOD2):c.2719T>C (p.Trp907Arg) rs104895490
NM_022162.3(NOD2):c.2739C>T (p.Asp913=) rs104895451
NM_022162.3(NOD2):c.2753C>A (p.Ala918Asp) rs104895452
NM_022162.3(NOD2):c.2771G>A (p.Gly924Asp) rs104895453
NM_022162.3(NOD2):c.2817T>C (p.Ile939=) rs104895454
NM_022162.3(NOD2):c.2863G>A (p.Val955Ile) rs5743291
NM_022162.3(NOD2):c.2914G>A (p.Val972Ile) rs104895455
NM_022162.3(NOD2):c.2925C>T (p.Leu975=) rs104895463
NM_022162.3(NOD2):c.2933G>A (p.Gly978Glu) rs104895457
NM_022162.3(NOD2):c.3051-102C>G rs104895458
NM_022162.3(NOD2):c.3055C>T (p.Arg1019Ter) rs104895491
NM_022162.3(NOD2):c.315G>A (p.Ala105=) rs104895419
NM_022162.3(NOD2):c.337G>A (p.Asp113Asn) rs104895468
NM_022162.3(NOD2):c.357G>T (p.Leu119=) rs672601267
NM_022162.3(NOD2):c.413G>A (p.Arg138Gln) rs104895456
NM_022162.3(NOD2):c.469T>C (p.Trp157Arg) rs104895420
NM_022162.3(NOD2):c.703C>T (p.Arg235Cys) rs104895422
NM_022162.3(NOD2):c.74-7T>A rs104895421
NM_022162.3(NOD2):c.743T>G (p.Leu248Arg) rs104895423
NM_022162.3(NOD2):c.871G>A (p.Asp291Asn) rs104895424
NM_022162.3(NOD2):c.881C>G (p.Thr294Ser) rs104895425
NM_022162.3(NOD2):c.902C>T (p.Ala301Val) rs104895426
NM_022162.3(NOD2):c.931C>T (p.Arg311Trp) rs104895427

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