List of variants in gene TTN reported by Undiagnosed Diseases Network, NIH

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_001267550.2(TTN):c.82402A>C (p.Lys27468Gln)	rs201958805	0.00027
NM_001267550.2(TTN):c.39974-11T>G	rs758597536	0.00006
NM_001267550.2(TTN):c.16054G>A (p.Asp5352Asn)	rs1190242728	0.00001
NM_001267550.2(TTN):c.102956_102958del (p.Thr34319del)	rs878854378
NM_001267550.2(TTN):c.44516del (p.Asp14839fs)	rs2058865334
NM_001267550.2(TTN):c.62722C>T (p.Arg20908Ter)	rs543860009
NM_001267550.2(TTN):c.98994del (p.Lys32998fs)	rs727504535

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.