List of variants in gene SLX4 reported as likely benign by KCCC/NGS Laboratory, Kuwait Cancer Control Center

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: 13

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_032444.4(SLX4):c.2103G>C (p.Glu701Asp)	rs73505420	0.00210
NM_032444.4(SLX4):c.3676C>T (p.Arg1226Trp)	rs142008398	0.00114
NM_032444.4(SLX4):c.3774C>T (p.Pro1258=)	rs146054214	0.00085
NM_032444.4(SLX4):c.3189C>T (p.Gly1063=)	rs200742809	0.00047
NM_032444.4(SLX4):c.1470C>T (p.Leu490=)	rs139766312	0.00031
NM_032444.4(SLX4):c.86G>A (p.Arg29His)	rs149117119	0.00026
NM_032444.4(SLX4):c.833G>A (p.Arg278Gln)	rs201192909	0.00011
NM_032444.4(SLX4):c.1706C>T (p.Pro569Leu)	rs534528576	0.00007
NM_032444.4(SLX4):c.165C>T (p.Cys55=)	rs202030834	0.00006
NM_032444.4(SLX4):c.1896G>C (p.Gly632=)	rs200859735	0.00006
NM_032444.4(SLX4):c.4485G>C (p.Ala1495=)	rs140872903	0.00003
NM_032444.4(SLX4):c.426T>A (p.Gly142=)	rs377500336
NM_032444.4(SLX4):c.5250G>A (p.Ala1750=)	rs370495748

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.