List of variants in gene TXNL4A reported by GeneReviews

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 6

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NC_000018.9:g.77733765C>A	rs727502793
NC_000018.9:g.77748262delA	rs727502795
NC_000018.9:g.77748356G>A	rs727502794
NM_006701.2:c.Exon 3 deletion
NM_006701.5(TXNL4A):c.153+3A>G	rs879255559
NM_006701.5(TXNL4A):c.154-959_257+638del

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.