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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 36

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HGVS	dbSNP	gnomAD frequency
NM_003072.5(SMARCA4):c.2967C>T (p.Pro989=)	rs149874634	0.00051
NM_003072.5(SMARCA4):c.1791T>G (p.Pro597=)	rs141806282	0.00038
NM_003072.5(SMARCA4):c.2460C>T (p.Tyr820=)	rs372410282	0.00010
NM_003072.5(SMARCA4):c.3975C>T (p.Arg1325=)	rs144803359	0.00009
NM_003072.5(SMARCA4):c.1287G>A (p.Ala429=)	rs143600641	0.00006
NM_003072.5(SMARCA4):c.2438+10C>T	rs370782232	0.00006
NM_001387283.1(SMARCA4):c.4174A>G (p.Ile1392Val)	rs370424312	0.00005
NM_003072.5(SMARCA4):c.3830C>T (p.Pro1277Leu)	rs746219091	0.00004
NM_003072.5(SMARCA4):c.4585G>A (p.Val1529Ile)	rs777829717	0.00004
NM_003072.5(SMARCA4):c.4593C>T (p.Leu1531=)	rs757189400	0.00002
NM_003072.5(SMARCA4):c.254C>T (p.Ser85Leu)	rs751542188	0.00001
NM_003072.5(SMARCA4):c.305G>T (p.Gly102Val)	rs746602808	0.00001
NM_003072.5(SMARCA4):c.3546+9G>A	rs544551192	0.00001
NM_003072.5(SMARCA4):c.4152G>A (p.Thr1384=)	rs372620534	0.00001
NM_003072.5(SMARCA4):c.4834G>A (p.Gly1612Ser)	rs372319442	0.00001
NM_003072.5(SMARCA4):c.*9A>T	rs369766168
NM_003072.5(SMARCA4):c.1118+7del	rs774132615
NM_003072.5(SMARCA4):c.1521_1523dup (p.His508dup)	rs2145940595
NM_003072.5(SMARCA4):c.2048C>T (p.Pro683Leu)	rs878854203
NM_003072.5(SMARCA4):c.2559C>A (p.Phe853Leu)
NM_003072.5(SMARCA4):c.2584T>G (p.Tyr862Asp)	rs2146375696
NM_003072.5(SMARCA4):c.2647G>A (p.Gly883Ser)	rs1568486679
NM_003072.5(SMARCA4):c.2837C>G (p.Pro946Arg)	rs1555778830
NM_003072.5(SMARCA4):c.2859+8T>G	rs1555778883
NM_003072.5(SMARCA4):c.2890ATC[1] (p.Ile965del)	rs797045979
NM_003072.5(SMARCA4):c.2896C>T (p.Arg966Trp)	rs1227826852
NM_003072.5(SMARCA4):c.2936G>A (p.Arg979Gln)
NM_003072.5(SMARCA4):c.3021C>T (p.Leu1007=)	rs1555780015
NM_003072.5(SMARCA4):c.3067G>A (p.Glu1023Lys)	rs1555780047
NM_003072.5(SMARCA4):c.3475G>A (p.Gly1159Arg)	rs2146600812
NM_003072.5(SMARCA4):c.3732C>T (p.Arg1244=)	rs797045983
NM_003072.5(SMARCA4):c.3783C>G (p.His1261Gln)	rs797045985
NM_003072.5(SMARCA4):c.4303G>A (p.Asp1435Asn)	rs796506759
NM_003072.5(SMARCA4):c.4414T>G (p.Tyr1472Asp)	rs797045986
NM_003072.5(SMARCA4):c.4620C>T (p.Asn1540=)	rs751869068
NM_003072.5(SMARCA4):c.791G>C (p.Gly264Ala)	rs797045988

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