ClinVar Miner

List of variants in gene NF2 reported as uncertain significance for Neurofibromatosis, type 2

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 231
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HGVS dbSNP
NC_000022.10:g.(?_29999982)_(30000107_?)dup
NC_000022.10:g.(?_30050640)_(30050720_?)del
NC_000022.10:g.(?_30090731)_(30090801_?)dup
NM_000268.3(NF2):c.*1007C>A rs886057350
NM_000268.3(NF2):c.*106C>T rs886057338
NM_000268.3(NF2):c.*109G>T rs886057339
NM_000268.3(NF2):c.*1111G>T rs886057351
NM_000268.3(NF2):c.*1260dupC rs886057352
NM_000268.3(NF2):c.*1264C>T rs879093980
NM_000268.3(NF2):c.*1264delC rs886057353
NM_000268.3(NF2):c.*1287dupT rs886057354
NM_000268.3(NF2):c.*1294T>G rs886057355
NM_000268.3(NF2):c.*1297A>G rs886057356
NM_000268.3(NF2):c.*1326T>C rs886057358
NM_000268.3(NF2):c.*136G>A rs886057340
NM_000268.3(NF2):c.*1439T>C rs886057359
NM_000268.3(NF2):c.*1522C>A rs886057360
NM_000268.3(NF2):c.*1559C>A rs886057361
NM_000268.3(NF2):c.*158T>C rs886057341
NM_000268.3(NF2):c.*1652G>T rs751068883
NM_000268.3(NF2):c.*1672C>T rs757272448
NM_000268.3(NF2):c.*1737C>A rs886057362
NM_000268.3(NF2):c.*1782T>C rs886057363
NM_000268.3(NF2):c.*1848C>T rs886057364
NM_000268.3(NF2):c.*199C>A rs886057342
NM_000268.3(NF2):c.*2003T>G rs886057367
NM_000268.3(NF2):c.*2007delT rs886057365
NM_000268.3(NF2):c.*2007dupT rs886057365
NM_000268.3(NF2):c.*2010G>T rs886057368
NM_000268.3(NF2):c.*2020C>T rs886057370
NM_000268.3(NF2):c.*2021dupT rs886057369
NM_000268.3(NF2):c.*2031_*2032dupTT rs11442202
NM_000268.3(NF2):c.*2039dupG rs886057371
NM_000268.3(NF2):c.*2068G>T rs886057372
NM_000268.3(NF2):c.*2205G>A rs886057373
NM_000268.3(NF2):c.*2206G>A rs886057374
NM_000268.3(NF2):c.*2310C>T rs777037756
NM_000268.3(NF2):c.*2365C>T rs765602116
NM_000268.3(NF2):c.*2373C>A rs886057375
NM_000268.3(NF2):c.*2396G>T rs886057376
NM_000268.3(NF2):c.*2499C>A rs569992376
NM_000268.3(NF2):c.*266G>T rs886057343
NM_000268.3(NF2):c.*2670C>A rs763727745
NM_000268.3(NF2):c.*2753A>G rs199805259
NM_000268.3(NF2):c.*2803C>A rs886057377
NM_000268.3(NF2):c.*293C>A rs886057344
NM_000268.3(NF2):c.*2999G>C rs886057378
NM_000268.3(NF2):c.*3018C>T rs886057379
NM_000268.3(NF2):c.*3055C>T rs886057380
NM_000268.3(NF2):c.*3107T>G rs886057381
NM_000268.3(NF2):c.*3140G>T rs886057382
NM_000268.3(NF2):c.*3189G>T rs886057383
NM_000268.3(NF2):c.*3266C>A rs886057384
NM_000268.3(NF2):c.*3298G>T rs886057385
NM_000268.3(NF2):c.*3319delG rs372162228
NM_000268.3(NF2):c.*335C>T rs886057345
NM_000268.3(NF2):c.*3443G>T rs886057387
NM_000268.3(NF2):c.*3480T>G rs886057388
NM_000268.3(NF2):c.*3613_*3618delCAAGCC rs755969033
NM_000268.3(NF2):c.*3646C>T rs886057390
NM_000268.3(NF2):c.*3670C>T rs886057391
NM_000268.3(NF2):c.*3715C>A rs886057392
NM_000268.3(NF2):c.*3783T>C rs886057393
NM_000268.3(NF2):c.*388C>T rs777219109
NM_000268.3(NF2):c.*532G>T rs886057346
NM_000268.3(NF2):c.*561C>G rs776610927
NM_000268.3(NF2):c.*573C>T rs543669369
NM_000268.3(NF2):c.*587G>T rs886057347
NM_000268.3(NF2):c.*768_*769dupAG rs886057348
NM_000268.3(NF2):c.*987C>A rs886057349
NM_000268.3(NF2):c.-142del rs1569259403
NM_000268.3(NF2):c.-245C>G rs536438675
NM_000268.3(NF2):c.-268G>T rs886057335
NM_000268.3(NF2):c.-284C>A rs886057334
NM_000268.3(NF2):c.-320C>T rs886057333
NM_000268.3(NF2):c.-397C>T rs886057332
NM_000268.3(NF2):c.-402A>G rs886057331
NM_000268.3(NF2):c.1000-7C>G rs776237839
NM_000268.3(NF2):c.1000A>G (p.Met334Val) rs1556000094
NM_000268.3(NF2):c.1012C>T (p.Arg338Cys) rs761795291
NM_000268.3(NF2):c.1013G>A (p.Arg338His) rs768053145
NM_000268.3(NF2):c.1018G>A (p.Ala340Thr) rs780430071
NM_000268.3(NF2):c.1018G>T (p.Ala340Ser) rs780430071
NM_000268.3(NF2):c.1022G>A (p.Arg341Gln) rs754087071
NM_000268.3(NF2):c.1037G>A (p.Arg346Lys) rs1556000154
NM_000268.3(NF2):c.1052G>A (p.Arg351His) rs771675702
NM_000268.3(NF2):c.1053C>T (p.Arg351=) rs1179494821
NM_000268.3(NF2):c.1055C>T (p.Thr352Met)
NM_000268.3(NF2):c.1059G>C (p.Arg353Ser) rs1379674036
NM_000268.3(NF2):c.1103C>T (p.Thr368Ile) rs1556000214
NM_000268.3(NF2):c.1113C>G (p.Asn371Lys)
NM_000268.3(NF2):c.111C>T (p.Cys37=) rs1302428933
NM_000268.3(NF2):c.1123-7C>G
NM_000268.3(NF2):c.1124T>C (p.Met375Thr) rs1556000763
NM_000268.3(NF2):c.1127G>A (p.Arg376Gln) rs996964764
NM_000268.3(NF2):c.1129T>G (p.Ser377Ala) rs1569305865
NM_000268.3(NF2):c.114+6C>G rs1060503671
NM_000268.3(NF2):c.1231C>T (p.Arg411Cys)
NM_000268.3(NF2):c.1232G>A (p.Arg411His) rs201214090
NM_000268.3(NF2):c.1252C>T (p.Arg418Cys)
NM_000268.3(NF2):c.1253G>A (p.Arg418His) rs548217466
NM_000268.3(NF2):c.1270C>A (p.Arg424Ser)
NM_000268.3(NF2):c.1270C>G (p.Arg424Gly) rs763826793
NM_000268.3(NF2):c.1270C>T (p.Arg424Cys)
NM_000268.3(NF2):c.1271G>T (p.Arg424Leu) rs751182657
NM_000268.3(NF2):c.1288G>T (p.Val430Leu) rs1361867592
NM_000268.3(NF2):c.1300G>A (p.Glu434Lys) rs992662337
NM_000268.3(NF2):c.1301A>G (p.Glu434Gly)
NM_000268.3(NF2):c.1303G>T (p.Val435Leu) rs772334382
NM_000268.3(NF2):c.1340+6G>T
NM_000268.3(NF2):c.1357C>G (p.Gln453Glu) rs1556001358
NM_000268.3(NF2):c.1364A>G (p.Lys455Arg) rs1318882444
NM_000268.3(NF2):c.1385G>A (p.Arg462His) rs373650983
NM_000268.3(NF2):c.1386C>T (p.Arg462=) rs138354622
NM_000268.3(NF2):c.1387G>A (p.Glu463Lys) rs74315503
NM_000268.3(NF2):c.1391C>T (p.Ala464Val) rs776109136
NM_000268.3(NF2):c.1396C>G (p.Arg466Gly) rs74315504
NM_000268.3(NF2):c.1397G>A (p.Arg466Gln) rs866689896
NM_000268.3(NF2):c.1400G>A (p.Arg467Lys)
NM_000268.3(NF2):c.1439C>T (p.Thr480Met) rs145666157
NM_000268.3(NF2):c.1445C>T (p.Pro482Leu) rs766339217
NM_000268.3(NF2):c.1446+5G>A rs367829184
NM_000268.3(NF2):c.1446+6C>A rs878853924
NM_000268.3(NF2):c.1446G>A (p.Pro482=) rs753751373
NM_000268.3(NF2):c.1450A>G (p.Met484Val) rs1182896077
NM_000268.3(NF2):c.1451T>C (p.Met484Thr) rs141538143
NM_000268.3(NF2):c.1460T>C (p.Ile487Thr)
NM_000268.3(NF2):c.1468C>T (p.Pro490Ser)
NM_000268.3(NF2):c.1469C>T (p.Pro490Leu)
NM_000268.3(NF2):c.1484T>G (p.Ile495Arg) rs1556002511
NM_000268.3(NF2):c.1490G>C (p.Ser497Thr) rs900545157
NM_000268.3(NF2):c.1501A>G (p.Ile501Val) rs1315864916
NM_000268.3(NF2):c.1502T>C (p.Ile501Thr) rs767682136
NM_000268.3(NF2):c.1511G>A (p.Ser504Asn)
NM_000268.3(NF2):c.1517C>G (p.Ser506Cys)
NM_000268.3(NF2):c.1529A>G (p.Lys510Arg) rs886057337
NM_000268.3(NF2):c.1540A>G (p.Met514Val) rs201527155
NM_000268.3(NF2):c.1547G>A (p.Arg516Gln) rs1569309694
NM_000268.3(NF2):c.1557G>A (p.Met519Ile)
NM_000268.3(NF2):c.1575A>G (p.Lys525=) rs1060503673
NM_000268.3(NF2):c.157A>G (p.Thr53Ala)
NM_000268.3(NF2):c.1586T>C (p.Met529Thr) rs780818183
NM_000268.3(NF2):c.15C>G (p.Ile5Met)
NM_000268.3(NF2):c.1611G>T (p.Glu537Asp)
NM_000268.3(NF2):c.1619A>G (p.Asn540Ser)
NM_000268.3(NF2):c.1635A>T (p.Glu545Asp) rs1556003698
NM_000268.3(NF2):c.1656_1657AG[2] (p.Arg554fs)
NM_000268.3(NF2):c.1678A>G (p.Ile560Val)
NM_000268.3(NF2):c.1685A>T (p.His562Leu) rs878853926
NM_000268.3(NF2):c.1688A>G (p.Asn563Ser)
NM_000268.3(NF2):c.1693A>T (p.Asn565Tyr)
NM_000268.3(NF2):c.1699G>A (p.Asp567Asn) rs757586383
NM_000268.3(NF2):c.1701C>G (p.Asp567Glu) rs1049732514
NM_000268.3(NF2):c.1702A>G (p.Arg568Gly)
NM_000268.3(NF2):c.1702_1703del (p.Arg568fs)
NM_000268.3(NF2):c.170G>A (p.Arg57Gln) rs368773485
NM_000268.3(NF2):c.1724A>G (p.Asn575Ser) rs1569312127
NM_000268.3(NF2):c.1737+2098A>G rs75296199
NM_000268.3(NF2):c.1737G>A (p.Lys579=) rs1569312133
NM_000268.3(NF2):c.1738-4_1741delinsG rs1556008383
NM_000268.3(NF2):c.1739_1747delTCACCTTGC rs1060503674
NM_000268.3(NF2):c.1765G>A (p.Val589Met) rs1293851600
NM_000268.3(NF2):c.1774T>C (p.Phe592Leu) rs764972504
NM_000268.3(NF2):c.1783C>T (p.Leu595Phe)
NM_000268.3(NF2):c.196T>A (p.Tyr66Asn) rs772274240
NM_000268.3(NF2):c.215T>C (p.Val72Ala) rs1260510937
NM_000268.3(NF2):c.243_248del (p.Leu82_Asp83del) rs777858863
NM_000268.3(NF2):c.271C>A (p.Pro91Thr) rs1555987645
NM_000268.3(NF2):c.272C>A (p.Pro91Gln) rs1569281659
NM_000268.3(NF2):c.293C>A (p.Ala98Asp) rs1060503668
NM_000268.3(NF2):c.296A>G (p.Lys99Arg)
NM_000268.3(NF2):c.300T>A (p.Phe100Leu) rs1555987677
NM_000268.3(NF2):c.302A>T (p.Tyr101Phe) rs1240469044
NM_000268.3(NF2):c.305C>G (p.Pro102Arg)
NM_000268.3(NF2):c.326T>C (p.Leu109Pro)
NM_000268.3(NF2):c.328G>C (p.Val110Leu)
NM_000268.3(NF2):c.343C>G (p.Gln115Glu)
NM_000268.3(NF2):c.345A>T (p.Gln115His) rs746369012
NM_000268.3(NF2):c.347A>G (p.His116Arg)
NM_000268.3(NF2):c.349T>G (p.Leu117Val) rs1569281810
NM_000268.3(NF2):c.363+3A>T rs1060503669
NM_000268.3(NF2):c.370A>C (p.Lys124Gln)
NM_000268.3(NF2):c.391A>C (p.Ile131Leu) rs878853927
NM_000268.3(NF2):c.3_14del (p.Met1_Ala4del) rs1351718417
NM_000268.3(NF2):c.400C>T (p.Pro134Ser) rs1555988776
NM_000268.3(NF2):c.401C>T (p.Pro134Leu) rs1029716358
NM_000268.3(NF2):c.436G>A (p.Val146Ile)
NM_000268.3(NF2):c.457T>C (p.Tyr153His)
NM_000268.3(NF2):c.478C>T (p.Arg160Trp) rs150667239
NM_000268.3(NF2):c.479G>A (p.Arg160Gln)
NM_000268.3(NF2):c.495A>G (p.Gln165=)
NM_000268.3(NF2):c.497A>T (p.Glu166Val)
NM_000268.3(NF2):c.4G>T (p.Ala2Ser)
NM_000268.3(NF2):c.515G>A (p.Arg172Lys)
NM_000268.3(NF2):c.521T>C (p.Ile174Thr) rs1346860299
NM_000268.3(NF2):c.560G>A (p.Arg187Lys) rs1234052589
NM_000268.3(NF2):c.595G>A (p.Ala199Thr) rs1261707371
NM_000268.3(NF2):c.599+3G>A rs768301915
NM_000268.3(NF2):c.602A>T (p.Asp201Val)
NM_000268.3(NF2):c.610G>C (p.Glu204Gln) rs1569295916
NM_000268.3(NF2):c.613A>G (p.Met205Val) rs141629512
NM_000268.3(NF2):c.614T>C (p.Met205Thr) rs747871414
NM_000268.3(NF2):c.652G>A (p.Gly218Ser)
NM_000268.3(NF2):c.662A>G (p.Tyr221Cys)
NM_000268.3(NF2):c.670A>G (p.Ile224Val)
NM_000268.3(NF2):c.675G>T (p.Arg225=) rs1569295986
NM_000268.3(NF2):c.676-10G>A
NM_000268.3(NF2):c.676A>C (p.Asn226His) rs886057336
NM_000268.3(NF2):c.683A>G (p.Lys228Arg) rs145384260
NM_000268.3(NF2):c.685G>T (p.Gly229Cys)
NM_000268.3(NF2):c.713C>T (p.Ala238Val)
NM_000268.3(NF2):c.726C>G (p.His242Gln)
NM_000268.3(NF2):c.736C>T (p.Pro246Ser) rs1569297802
NM_000268.3(NF2):c.749T>A (p.Leu250Gln) rs1432132718
NM_000268.3(NF2):c.74G>A (p.Arg25Lys) rs1569259813
NM_000268.3(NF2):c.758A>G (p.Lys253Arg)
NM_000268.3(NF2):c.770C>T (p.Pro257Leu)
NM_000268.3(NF2):c.772T>G (p.Trp258Gly)
NM_000268.3(NF2):c.810+8_810+9delAT rs760095910
NM_000268.3(NF2):c.810_810+2dup rs1569297926
NM_000268.3(NF2):c.817A>G (p.Ile273Val) rs1368184325
NM_000268.3(NF2):c.851A>G (p.Lys284Arg)
NM_000268.3(NF2):c.872G>A (p.Arg291His)
NM_000268.3(NF2):c.885+6T>C
NM_000268.3(NF2):c.904G>A (p.Gly302Arg) rs1255367068
NM_000268.3(NF2):c.911A>G (p.His304Arg) rs1555998800
NM_000268.3(NF2):c.932G>A (p.Arg311Lys) rs1169276398
NM_000268.3(NF2):c.947T>G (p.Leu316Trp) rs750633919
NM_000268.3(NF2):c.983A>T (p.Glu328Val) rs200372028
NM_016418.5(NF2):c.1751G>A (p.Gly584Asp)
Single allele

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