ClinVar Miner

List of variants in gene SMARCA4 reported as uncertain significance by Fulgent Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
Download table as spreadsheet
HGVS dbSNP
NM_001128849.1(SMARCA4):c.1018G>A (p.Ala340Thr) rs371214327
NM_001128849.1(SMARCA4):c.1098C>G (p.Ile366Met) rs532242119
NM_001128849.1(SMARCA4):c.1108C>T (p.Arg370Cys) rs1436490540
NM_001128849.1(SMARCA4):c.1889G>A (p.Gly630Asp) rs749533909
NM_001128849.1(SMARCA4):c.2438+4A>C
NM_001128849.1(SMARCA4):c.3436G>A (p.Gly1146Ser) rs200007170
NM_001128849.1(SMARCA4):c.3830C>T (p.Pro1277Leu) rs746219091
NM_001128849.1(SMARCA4):c.407C>T (p.Ala136Val) rs535299273
NM_001128849.1(SMARCA4):c.422C>T (p.Ser141Leu) rs1060502073
NM_001128849.1(SMARCA4):c.4351G>A (p.Ala1451Thr) rs374722116
NM_001128849.1(SMARCA4):c.4472C>T (p.Thr1491Ile) rs1555788341
NM_001128849.1(SMARCA4):c.4520+6C>T rs778283753
NM_001128849.1(SMARCA4):c.4913A>G (p.Gln1638Arg) rs878854231
NM_001128849.1(SMARCA4):c.4922T>C (p.Leu1641Pro) rs755493468
NM_001128849.1(SMARCA4):c.4967C>T (p.Pro1656Leu) rs756255060
NM_001128849.1(SMARCA4):c.4972G>A (p.Val1658Met) rs757412819
NM_001128849.1(SMARCA4):c.709G>A (p.Gly237Ser) rs1555753727
NM_001128849.1(SMARCA4):c.778A>C (p.Met260Leu) rs1064795842
NM_001128849.1(SMARCA4):c.829C>T (p.Pro277Ser) rs767947665
NM_001128849.1(SMARCA4):c.914C>T (p.Pro305Leu) rs138097741
NM_001128849.1(SMARCA4):c.952G>A (p.Val318Ile) rs758091260

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.