ClinVar Miner

List of variants in gene PRRT2 reported as benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
Download table as spreadsheet
NM_145239.3(PRRT2):c.*11C>T rs201814968
NM_145239.3(PRRT2):c.1013-29C>T rs745834081
NM_145239.3(PRRT2):c.225G>A (p.Pro75=) rs199662641
NM_145239.3(PRRT2):c.412C>G (p.Pro138Ala) rs79182085
NM_145239.3(PRRT2):c.439G>C (p.Asp147His) rs79568162
NM_145239.3(PRRT2):c.564G>A (p.Gln188=) rs545201760
NM_145239.3(PRRT2):c.612C>G (p.Pro204=) rs149260055
NM_145239.3(PRRT2):c.640G>C (p.Ala214Pro) rs745594874
NM_145239.3(PRRT2):c.644C>G (p.Pro215Arg) rs200926711
NM_145239.3(PRRT2):c.645C>T (p.Pro215=) rs183683129
NM_145239.3(PRRT2):c.647C>T (p.Pro216Leu) rs76335820
NM_145239.3(PRRT2):c.67G>A (p.Glu23Lys) rs140383655
NM_145239.3(PRRT2):c.696C>T (p.His232=) rs570108715
NM_145239.3(PRRT2):c.751= (p.Leu251=) rs11150573
NM_145239.3(PRRT2):c.751T>C (p.Leu251=) rs11150573
NM_145239.3(PRRT2):c.773G>A (p.Gly258Glu) rs560303559
NM_145239.3(PRRT2):c.828C>T (p.Cys276=) rs35625748
NM_145239.3(PRRT2):c.880-11C>T rs769037377
NM_145239.3(PRRT2):c.880-14C>T rs148323840
NM_145239.3(PRRT2):c.960G>A (p.Ala320=) rs753833531

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.