ClinVar Miner

List of variants in gene SMARCA4 reported as likely benign by Genetic Services Laboratory, University of Chicago

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Total variants: 21
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HGVS dbSNP
NM_001128849.2(SMARCA4):c.*1G>T rs76118382
NM_001128849.2(SMARCA4):c.1114T>C (p.Tyr372His) rs140192268
NM_001128849.2(SMARCA4):c.1119-6T>C rs368180712
NM_001128849.2(SMARCA4):c.1236C>T (p.Phe412=) rs140000691
NM_001128849.2(SMARCA4):c.1413G>A (p.Lys471=) rs17001073
NM_001128849.2(SMARCA4):c.1419+8C>T rs115492175
NM_001128849.2(SMARCA4):c.1419+9C>T rs374635008
NM_001128849.2(SMARCA4):c.1509A>G (p.Ala503=) rs17001075
NM_001128849.2(SMARCA4):c.1748A>G (p.Lys583Arg) rs1043517699
NM_001128849.2(SMARCA4):c.223-5C>T rs376775933
NM_001128849.2(SMARCA4):c.2418C>T (p.Phe806=) rs770432256
NM_001128849.2(SMARCA4):c.2739G>A (p.Pro913=) rs183695281
NM_001128849.2(SMARCA4):c.3168+31C>G rs2075021
NM_001128849.2(SMARCA4):c.3894C>T (p.Asp1298=) rs373041389
NM_001128849.2(SMARCA4):c.4590C>T (p.Tyr1530=) rs139505007
NM_001128849.2(SMARCA4):c.4680C>T (p.Asp1560=) rs9105
NM_001128849.2(SMARCA4):c.708T>C (p.Pro236=) rs62639303
NM_001128849.2(SMARCA4):c.722_733del (p.229_230GP[6]) rs568390760
NM_001128849.2(SMARCA4):c.747C>T (p.Tyr249=) rs756224211
NM_001128849.2(SMARCA4):c.915G>A (p.Pro305=) rs149573400
NM_001128849.2(SMARCA4):c.930C>A (p.Arg310=) rs146141457

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