List of variants in gene SNRNP200 reported as benign for not specified

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: 11

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_014014.5(SNRNP200):c.5755-20A>G	rs3214063	0.31866
NM_014014.5(SNRNP200):c.5933G>C (p.Gly1978Ala)	rs75956769	0.00593
NM_014014.5(SNRNP200):c.1159A>G (p.Met387Val)	rs142729495	0.00369
NM_014014.5(SNRNP200):c.3654C>T (p.Ser1218=)	rs3214060	0.00353
NM_014014.5(SNRNP200):c.4165G>A (p.Val1389Ile)	rs143898031	0.00328
NM_014014.5(SNRNP200):c.5766C>T (p.Leu1922=)	rs147427344	0.00133
NM_014014.5(SNRNP200):c.2800A>G (p.Thr934Ala)	rs149616320	0.00042
NM_014014.5(SNRNP200):c.1203+9C>T	rs753985092	0.00016
NM_014014.5(SNRNP200):c.5538C>T (p.Ile1846=)	rs201513678	0.00015
NM_014014.5(SNRNP200):c.3897C>G (p.Thr1299=)	rs144934076
NM_014014.5(SNRNP200):c.732C>T (p.Leu244=)	rs199688602

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.