ClinVar Miner

List of variants in gene SMARCA4 reported as uncertain significance by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
Download table as spreadsheet
HGVS dbSNP
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.296G>A (p.Arg99Gln) rs745406632
NM_001128849.2(SMARCA4):c.335C>T (p.Pro112Leu) rs1057523400
NM_001128849.2(SMARCA4):c.3791C>T (p.Thr1264Met) rs377119410
NM_001128849.2(SMARCA4):c.3873+5G>C rs1057522951
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.4681G>A (p.Val1561Ile) rs777829717
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.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

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.