ClinVar Miner

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

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Total variants: 24
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HGVS dbSNP
NM_001128849.2(SMARCA4):c.1118+7del rs774132615
NM_001128849.2(SMARCA4):c.1287G>A (p.Ala429=) rs143600641
NM_001128849.2(SMARCA4):c.1791T>G (p.Pro597=) rs141806282
NM_001128849.2(SMARCA4):c.2438+10C>T rs370782232
NM_001128849.2(SMARCA4):c.2460C>T (p.Tyr820=) rs372410282
NM_001128849.2(SMARCA4):c.2837C>G (p.Pro946Arg) rs1555778830
NM_001128849.2(SMARCA4):c.2859+8T>G rs1555778883
NM_001128849.2(SMARCA4):c.2890_2892ATC[1] (p.Ile965del) rs797045979
NM_001128849.2(SMARCA4):c.2896C>T (p.Arg966Trp) rs1227826852
NM_001128849.2(SMARCA4):c.2936G>A (p.Arg979Gln) rs797045981
NM_001128849.2(SMARCA4):c.2967C>T (p.Pro989=) rs149874634
NM_001128849.2(SMARCA4):c.3021C>T (p.Leu1007=) rs1555780015
NM_001128849.2(SMARCA4):c.3546+9G>A rs544551192
NM_001128849.2(SMARCA4):c.3732C>T (p.Arg1244=) rs797045983
NM_001128849.2(SMARCA4):c.3783C>G (p.His1261Gln) rs797045985
NM_001128849.2(SMARCA4):c.3830C>T (p.Pro1277Leu) rs746219091
NM_001128849.2(SMARCA4):c.3975C>T (p.Arg1325=) rs144803359
NM_001128849.2(SMARCA4):c.4152G>A (p.Thr1384=) rs372620534
NM_001128849.2(SMARCA4):c.4174A>G (p.Ile1392Val) rs370424312
NM_001128849.2(SMARCA4):c.4510T>G (p.Tyr1504Asp) rs797045986
NM_001128849.2(SMARCA4):c.4681G>A (p.Val1561Ile) rs777829717
NM_001128849.2(SMARCA4):c.4689C>T (p.Leu1563=) rs757189400
NM_001128849.2(SMARCA4):c.4930G>A (p.Gly1644Ser) rs372319442
NM_001128849.2(SMARCA4):c.791G>C (p.Gly264Ala) rs797045988

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