List of variants in gene SALL1 reported as benign by EGL Genetic Diagnostics,Eurofins Clinical Diagnostics

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

Total variants: 10

Download table as spreadsheet

HGVS	dbSNP
NM_001127892.1(SALL1):c.157_159AGC[7] (p.Ser60_Ser62del)	rs113614842
NM_001127892.1(SALL1):c.187_189GGC[5] (p.Gly66dup)	rs1555475414
NM_002968.2(SALL1):c.235G>C (p.Ala79Pro)	rs536108231
NM_002968.2(SALL1):c.2574C>T (p.Leu858=)	rs1965024
NM_002968.2(SALL1):c.3915C>T (p.Asn1305=)	rs140524372
NM_002968.2(SALL1):c.466_477dup (p.Ser159_Gly160insSerSerSerSer)	rs113614842
NM_002968.2(SALL1):c.472A>G (p.Ser158Gly)	rs139646526
NM_002968.2(SALL1):c.475_477delAGC	rs113614842
NM_002968.2(SALL1):c.809C>T (p.Pro270Leu)	rs140827311
NM_002968.3(SALL1):c.448_450AGC[12] (p.Ser158_Ser159dup)	rs113614842

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.