ClinVar Miner

List of variants in gene SMARCA4 reported as benign

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Total variants: 72
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HGVS dbSNP
NM_001128849.1(SMARCA4):c.*1G>T rs76118382
NM_001128849.1(SMARCA4):c.1098C>T (p.Ile366=) rs532242119
NM_001128849.1(SMARCA4):c.1099C>T (p.Leu367=) rs372379166
NM_001128849.1(SMARCA4):c.1114T>C (p.Tyr372His) rs140192268
NM_001128849.1(SMARCA4):c.1140C>T (p.His380=) rs114594206
NM_001128849.1(SMARCA4):c.1209G>A (p.Glu403=) rs200159174
NM_001128849.1(SMARCA4):c.120C>T (p.His40=) rs375884151
NM_001128849.1(SMARCA4):c.1413G>A (p.Lys471=) rs17001073
NM_001128849.1(SMARCA4):c.1419+7T>C rs112977340
NM_001128849.1(SMARCA4):c.1419+8C>T rs115492175
NM_001128849.1(SMARCA4):c.1419+9C>T rs374635008
NM_001128849.1(SMARCA4):c.1509A>G (p.Ala503=) rs17001075
NM_001128849.1(SMARCA4):c.1524T>C (p.His508=) rs7935
NM_001128849.1(SMARCA4):c.1557C>T (p.Asn519=) rs2288845
NM_001128849.1(SMARCA4):c.1740A>G (p.Lys580=) rs114391904
NM_001128849.1(SMARCA4):c.1803G>A (p.Pro601=) rs751166438
NM_001128849.1(SMARCA4):c.1944-19G>T rs74942410
NM_001128849.1(SMARCA4):c.2001+8T>G rs112549813
NM_001128849.1(SMARCA4):c.2123+12C>T rs17001090
NM_001128849.1(SMARCA4):c.2199C>T (p.Ala733=) rs538629432
NM_001128849.1(SMARCA4):c.222+14T>C rs112825147
NM_001128849.1(SMARCA4):c.223-4G>A rs763383326
NM_001128849.1(SMARCA4):c.223-5C>T rs376775933
NM_001128849.1(SMARCA4):c.2275-3C>A rs117611401
NM_001128849.1(SMARCA4):c.2347C>T (p.Leu783=) rs762449855
NM_001128849.1(SMARCA4):c.2388C>T (p.Leu796=) rs28997580
NM_001128849.1(SMARCA4):c.2409T>C (p.Asn803=) rs199634608
NM_001128849.1(SMARCA4):c.2580C>T (p.Tyr860=) rs776649185
NM_001128849.1(SMARCA4):c.258C>T (p.Asp86=) rs115992445
NM_001128849.1(SMARCA4):c.2617-4G>A rs201020451
NM_001128849.1(SMARCA4):c.2739G>A (p.Pro913=) rs183695281
NM_001128849.1(SMARCA4):c.2757C>T (p.Pro919=) rs113955216
NM_001128849.1(SMARCA4):c.2763C>T (p.Leu921=) rs574844383
NM_001128849.1(SMARCA4):c.2817C>T (p.Phe939=) rs147791182
NM_001128849.1(SMARCA4):c.2967C>T (p.Pro989=) rs149874634
NM_001128849.1(SMARCA4):c.2974-4G>A rs766593089
NM_001128849.1(SMARCA4):c.3045C>T (p.Gly1015=) rs56101423
NM_001128849.1(SMARCA4):c.3066C>T (p.Ser1022=) rs149111403
NM_001128849.1(SMARCA4):c.3168+9G>A rs369201773
NM_001128849.1(SMARCA4):c.3383-5G>A rs762528243
NM_001128849.1(SMARCA4):c.3547-11T>C rs190104006
NM_001128849.1(SMARCA4):c.356-14A>G rs111447132
NM_001128849.1(SMARCA4):c.3663G>A (p.Lys1221=) rs61761957
NM_001128849.1(SMARCA4):c.3738C>T (p.Phe1246=) rs139943231
NM_001128849.1(SMARCA4):c.3765G>A (p.Glu1255=) rs183060137
NM_001128849.1(SMARCA4):c.3891C>G (p.Pro1297=) rs149562732
NM_001128849.1(SMARCA4):c.3927C>T (p.His1309=) rs148495641
NM_001128849.1(SMARCA4):c.4053C>T (p.Asp1351=) rs28997582
NM_001128849.1(SMARCA4):c.4152G>A (p.Thr1384=) rs372620534
NM_001128849.1(SMARCA4):c.4171-9T>A rs201309716
NM_001128849.1(SMARCA4):c.4323A>G (p.Ser1441=) rs61761958
NM_001128849.1(SMARCA4):c.4347C>T (p.Ser1449=) rs377057304
NM_001128849.1(SMARCA4):c.4368G>A (p.Pro1456=) rs114882905
NM_001128849.1(SMARCA4):c.4389C>T (p.Arg1463=) rs149670457
NM_001128849.1(SMARCA4):c.441C>T (p.Ser147=) rs201372858
NM_001128849.1(SMARCA4):c.4590C>T (p.Tyr1530=) rs139505007
NM_001128849.1(SMARCA4):c.459G>A (p.Pro153=) rs372931195
NM_001128849.1(SMARCA4):c.4680C>T (p.Asp1560=) rs9105
NM_001128849.1(SMARCA4):c.4731+12G>A rs34930626
NM_001128849.1(SMARCA4):c.4864+10G>A rs201665695
NM_001128849.1(SMARCA4):c.4869G>A (p.Arg1623=) rs568650875
NM_001128849.1(SMARCA4):c.4968G>A (p.Pro1656=) rs182644267
NM_001128849.1(SMARCA4):c.4983T>C (p.Asp1661=) rs7275
NM_001128849.1(SMARCA4):c.54G>A (p.Pro18=) rs529632222
NM_001128849.1(SMARCA4):c.589C>T (p.Pro197Ser) rs200664441
NM_001128849.1(SMARCA4):c.708T>C (p.Pro236=) rs62639303
NM_001128849.1(SMARCA4):c.747C>T (p.Tyr249=) rs756224211
NM_001128849.1(SMARCA4):c.859+7T>A rs141461778
NM_001128849.1(SMARCA4):c.915G>A (p.Pro305=) rs149573400
NM_001128849.1(SMARCA4):c.930C>A (p.Arg310=) rs146141457
NM_001128849.1(SMARCA4):c.942G>A (p.Ala314=) rs567283924
NM_001128849.1(SMARCA4):c.981A>C (p.Pro327=) rs547268941

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