List of variants in gene SMARCAL1 reported as benign by Illumina Laboratory Services, Illumina

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: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_014140.4(SMARCAL1):c.2070T>C (p.Thr690=)	rs2066527	0.09632
NM_014140.4(SMARCAL1):c.945C>G (p.Ser315Arg)	rs2066522	0.04137
NM_014140.4(SMARCAL1):c.1129G>C (p.Glu377Gln)	rs2066518	0.03294
NM_014140.4(SMARCAL1):c.127G>A (p.Ala43Thr)	rs2066524	0.01441
NM_014140.4(SMARCAL1):c.423T>C (p.Tyr141=)	rs35907255	0.00918
NM_014140.4(SMARCAL1):c.901C>G (p.Pro301Ala)	rs146084305	0.00795
NM_014140.4(SMARCAL1):c.1243A>G (p.Ser415Gly)	rs58848916	0.00728
NM_014140.4(SMARCAL1):c.341G>A (p.Arg114His)	rs11555797	0.00693
NM_014140.4(SMARCAL1):c.72A>G (p.Arg24=)	rs199805770	0.00001
NM_014140.4(SMARCAL1):c.1947C>T (p.Asp649=)	rs2066526
NM_014140.4(SMARCAL1):c.960C>T (p.Ala320=)	rs2066513

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.