List of variants in gene KANSL1 reported as uncertain significance 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: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_015443.4(KANSL1):c.*954C>G	rs150500194	0.00393
NM_015443.4(KANSL1):c.*1103dup	rs142756815
NM_015443.4(KANSL1):c.1234_1235dup	rs140510364
NM_015443.4(KANSL1):c.*1354dup	rs67641084
NM_015443.4(KANSL1):c.*1520dup	rs67801660
NM_015443.4(KANSL1):c.*1551del	rs767830420
NM_015443.4(KANSL1):c.*28ACTA[1]	rs767896466
NM_015443.4(KANSL1):c.-90+19C>G	rs1057516026
NM_015443.4(KANSL1):c.836A>T (p.Asp279Val)	rs1567762446

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.