ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
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.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.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.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.4819_4845del (p.Ser1607_Glu1615del) rs1555795951
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.76G>A (p.Ala26Thr) rs145867502
NM_001128849.2(SMARCA4):c.778A>C (p.Met260Leu) rs1064795842

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.