ClinVar Miner

List of variants in gene SMARCA4 reported as uncertain significance for not provided

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Total variants: 32
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HGVS dbSNP
GRCh37/hg19 19p13.2(chr19:11109514-11154117)x3
NM_001128844.2(SMARCA4):c.2275-3C>A rs117611401
NM_001128849.2(SMARCA4):c.223-5C>T rs376775933
NM_001128849.2(SMARCA4):c.2476G>A (p.Ala826Thr) rs1057524313
NM_001128849.2(SMARCA4):c.2541G>C (p.Gln847His) rs1064796361
NM_001128849.2(SMARCA4):c.258C>T (p.Asp86=) rs115992445
NM_001128849.2(SMARCA4):c.2850C>T (p.Thr950=) rs141259126
NM_001128849.2(SMARCA4):c.296G>A (p.Arg99Gln) rs745406632
NM_001128849.2(SMARCA4):c.335C>T (p.Pro112Leu) rs1057523400
NM_001128849.2(SMARCA4):c.3442G>C (p.Glu1148Gln) rs1555783190
NM_001128849.2(SMARCA4):c.3528C>T (p.Ser1176=) rs573885719
NM_001128849.2(SMARCA4):c.3791C>T (p.Thr1264Met) rs377119410
NM_001128849.2(SMARCA4):c.3873+5G>C rs1057522951
NM_001128849.2(SMARCA4):c.400G>T (p.Val134Phe) rs1057520203
NM_001128849.2(SMARCA4):c.4211T>G (p.Val1404Gly) rs200469979
NM_001128849.2(SMARCA4):c.4217G>A (p.Arg1406His) rs779801126
NM_001128849.2(SMARCA4):c.4284G>T (p.Thr1428=) rs199847974
NM_001128849.2(SMARCA4):c.4532G>A (p.Arg1511His) rs1057523566
NM_001128849.2(SMARCA4):c.4654C>T (p.Arg1552Cys) rs1057523119
NM_001128849.2(SMARCA4):c.4720G>C (p.Glu1574Gln) rs1057523176
NM_001128849.2(SMARCA4):c.4760C>T (p.Ser1587Leu) rs1057523990
NM_001128849.2(SMARCA4):c.4820G>A (p.Ser1607Asn) rs878854229
NM_001128849.2(SMARCA4):c.4968G>T (p.Pro1656=) rs182644267
NM_001128849.2(SMARCA4):c.608C>T (p.Ala203Val) rs780497718
NM_001128849.2(SMARCA4):c.696T>C (p.Pro232=) rs573767517
NM_001128849.2(SMARCA4):c.722_733dup (p.229_230GP[10]) rs568390760
NM_001128849.2(SMARCA4):c.76G>A (p.Ala26Thr) rs145867502
NM_001128849.2(SMARCA4):c.778A>C (p.Met260Leu) rs1064795842
NM_003072.4(SMARCA4):c.4723_4749del (p.Ser1575_Glu1583del) rs1555795951
NM_003072.4(SMARCA4):c.696_701TGGCCC[2] (p.229_230GP[7]) rs372601826
NM_003072.5(SMARCA4):c.3626G>A (p.Ser1209Asn)
NM_003072.5(SMARCA4):c.3826C>G (p.Pro1276Ala) rs1600393785

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