List of variants in gene TTC7A reported by Genome Diagnostics Laboratory, University Medical Center Utrecht

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: 7

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_020458.4(TTC7A):c.649-10C>T	rs149360779	0.00698
NM_020458.4(TTC7A):c.1095G>T (p.Val365=)	rs113844968	0.00279
NM_020458.4(TTC7A):c.2211G>A (p.Ala737=)	rs142959785	0.00177
NM_020458.4(TTC7A):c.1348G>A (p.Val450Met)	rs114276698	0.00136
NM_020458.4(TTC7A):c.2085C>G (p.Pro695=)	rs139460494	0.00095
NM_020458.4(TTC7A):c.1449G>A (p.Gly483=)	rs142810509	0.00024
NM_020458.4(TTC7A):c.1026C>T (p.Ile342=)	rs151317740

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.