List of variants in gene TAT reported as benign for not provided

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_000353.3(TAT):c.408+58A>C	rs2432520	0.65199
NM_000353.3(TAT):c.43C>T (p.Pro15Ser)	rs74344827	0.16609
NM_000353.3(TAT):c.1224+143A>G	rs1799881	0.11097
NM_000353.3(TAT):c.912+113T>C	rs2303226	0.09882
NM_000353.3(TAT):c.1125+270C>T	rs1364210	0.09763
NM_000353.3(TAT):c.309G>A (p.Ser103=)	rs78302875	0.07257
NM_000353.3(TAT):c.1173G>A (p.Glu391=)	rs16973331	0.04038
NM_000353.3(TAT):c.*110C>T	rs113110476	0.02095
NM_000353.3(TAT):c.1042-72G>T	rs172650

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.