List of variants in gene LYST reported by Eurofins NTD LLC (GA)

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: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000081.4(LYST):c.5945C>T (p.Thr1982Ile)	rs146591126	0.00669
NM_000081.4(LYST):c.10235G>A (p.Arg3412His)	rs148409403	0.00073
NM_000081.4(LYST):c.368A>G (p.His123Arg)	rs3768067	0.00027
NM_000081.4(LYST):c.9552G>T (p.Leu3184Phe)	rs556200563	0.00019
NM_000081.4(LYST):c.7862T>C (p.Met2621Thr)	rs368500877	0.00006
NM_000081.4(LYST):c.7780+2C>T	rs760108842	0.00001
NM_000081.4(LYST):c.11362C>T (p.Gln3788Ter)	rs1558092244
NM_000081.4(LYST):c.7070C>G (p.Ala2357Gly)	rs199576020

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.