ClinVar Miner

List of variants in gene SMARCA4 reported as benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 16
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HGVS dbSNP
NM_001128849.2(SMARCA4):c.1413G>A (p.Lys471=) rs17001073
NM_001128849.2(SMARCA4):c.1419+7T>C rs112977340
NM_001128849.2(SMARCA4):c.1419+8C>T rs115492175
NM_001128849.2(SMARCA4):c.1509A>G (p.Ala503=) rs17001075
NM_001128849.2(SMARCA4):c.1524T>C (p.His508=) rs7935
NM_001128849.2(SMARCA4):c.2123+12C>T rs17001090
NM_001128849.2(SMARCA4):c.222+14T>C rs112825147
NM_001128849.2(SMARCA4):c.2388C>T (p.Leu796=) rs28997580
NM_001128849.2(SMARCA4):c.3547-11T>C rs190104006
NM_001128849.2(SMARCA4):c.356-14A>G rs111447132
NM_001128849.2(SMARCA4):c.4053C>T (p.Asp1351=) rs28997582
NM_001128849.2(SMARCA4):c.4680C>T (p.Asp1560=) rs9105
NM_001128849.2(SMARCA4):c.4731+12G>A rs34930626
NM_001128849.2(SMARCA4):c.4983T>C (p.Asp1661=) rs7275
NM_001128849.2(SMARCA4):c.915G>A (p.Pro305=) rs149573400
NM_001128849.2(SMARCA4):c.930C>A (p.Arg310=) rs146141457

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