ClinVar Miner

List of variants in gene SMARCA4 reported as likely pathogenic for not provided

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Total variants: 18
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HGVS dbSNP
NM_001128849.2(SMARCA4):c.2143G>A (p.Asp715Asn) rs1131691371
NM_001128849.2(SMARCA4):c.2438C>T (p.Ser813Leu) rs1064795105
NM_001128849.2(SMARCA4):c.2593A>G (p.Lys865Glu) rs1057524208
NM_001128849.2(SMARCA4):c.2672G>A (p.Cys891Tyr) rs1555778709
NM_001128849.2(SMARCA4):c.2716C>T (p.Arg906Cys) rs898406635
NM_001128849.2(SMARCA4):c.2806T>A (p.Cys936Ser) rs1555778812
NM_001128849.2(SMARCA4):c.2900G>C (p.Arg967Pro) rs1085307769
NM_001128849.2(SMARCA4):c.2932C>G (p.Arg978Gly) rs1064796254
NM_001128849.2(SMARCA4):c.3070A>G (p.Lys1024Glu) rs1057524559
NM_001128849.2(SMARCA4):c.3380A>G (p.Asp1127Gly) rs1057521113
NM_001128849.2(SMARCA4):c.3577A>G (p.Ile1193Val) rs1555784468
NM_001128849.2(SMARCA4):c.3608G>A (p.Arg1203His) rs770680174
NM_001128849.2(SMARCA4):c.3641T>C (p.Ile1214Thr) rs1064796885
NM_001128849.2(SMARCA4):c.3724G>A (p.Glu1242Lys) rs1555784586
NM_001128849.2(SMARCA4):c.3728G>A (p.Arg1243Gln) rs1064795161
NM_001128849.2(SMARCA4):c.3951+1G>A rs1555785054
NM_001128849.2(SMARCA4):c.4309C>T (p.Arg1437Trp) rs1057518049
NM_003072.4(SMARCA4):c.3443_3448delinsGGC (p.Glu1148_Phe1150delinsGlyLeu) rs1064794535

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