List of variants in gene TRIT1 reported as pathogenic for Combined oxidative phosphorylation deficiency 35

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: 12

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_017646.6(TRIT1):c.979C>T (p.Arg327Ter)	rs144042123	0.00052
NM_017646.6(TRIT1):c.1256A>C (p.His419Pro)	rs566435653	0.00005
NM_017646.6(TRIT1):c.848T>G (p.Ile283Ser)	rs199622789	0.00004
NM_017646.6(TRIT1):c.326T>C (p.Ile109Thr)	rs146838322	0.00001
NM_017646.6(TRIT1):c.856A>G (p.Lys286Glu)	rs1060505019	0.00001
NM_017646.6(TRIT1):c.967C>T (p.Arg323Trp)	rs370866302	0.00001
NM_017646.6(TRIT1):c.968G>A (p.Arg323Gln)	rs1047420796	0.00001
NM_017646.6(TRIT1):c.1171_1172del (p.Lys391fs)
NM_017646.6(TRIT1):c.1204C>T (p.Arg402Ter)	rs367752391
NM_017646.6(TRIT1):c.334del (p.Arg112fs)	rs536000212
NM_017646.6(TRIT1):c.568C>T (p.Gln190Ter)	rs2124597984
NM_017646.6(TRIT1):c.882del (p.Glu295fs)

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.