List of variants in gene TRNT1 reported as uncertain significance by GeneDx

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: 17

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_182916.3(TRNT1):c.1292T>C (p.Ile431Thr)	rs150984011	0.00061
NM_182916.3(TRNT1):c.107A>T (p.Glu36Val)	rs138682354	0.00021
NM_182916.3(TRNT1):c.383A>G (p.Asp128Gly)	rs148398677	0.00020
NM_182916.3(TRNT1):c.259A>G (p.Thr87Ala)	rs140935012	0.00011
NM_182916.3(TRNT1):c.488A>T (p.Asp163Val)	rs146717589	0.00006
NM_182916.3(TRNT1):c.560C>T (p.Ala187Val)	rs1378826731	0.00003
NM_182916.3(TRNT1):c.900C>A (p.Phe300Leu)	rs376431679	0.00003
NM_182916.3(TRNT1):c.448C>T (p.Arg150Cys)	rs747332169	0.00002
NM_182916.3(TRNT1):c.1079C>T (p.Thr360Ile)	rs776480350	0.00001
NM_182916.3(TRNT1):c.821G>C (p.Ser274Thr)	rs762709856	0.00001
NM_182916.3(TRNT1):c.991A>G (p.Lys331Glu)	rs769261859	0.00001
NM_182916.3(TRNT1):c.1057-7C>G	rs368078167
NM_182916.3(TRNT1):c.1291A>G (p.Ile431Val)	rs142642881
NM_182916.3(TRNT1):c.1300A>T (p.Thr434Ser)	rs1219909785
NM_182916.3(TRNT1):c.130G>A (p.Gly44Arg)
NM_182916.3(TRNT1):c.147A>G (p.Thr49=)
NM_182916.3(TRNT1):c.631A>C (p.Lys211Gln)	rs372027157

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.