ClinVar Miner

List of variants in gene GRIN2A reported as pathogenic for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
Download table as spreadsheet
HGVS dbSNP
NM_000833.5(GRIN2A):c.1453del (p.His485fs) rs1555494781
NM_000833.5(GRIN2A):c.2041C>T (p.Arg681Ter) rs397518472
NM_000833.5(GRIN2A):c.2054T>G (p.Val685Gly) rs796052548
NM_000833.5(GRIN2A):c.2449A>G (p.Met817Val) rs796052551
NM_000833.5(GRIN2A):c.2450T>G (p.Met817Arg) rs1064796608
NM_000833.5(GRIN2A):c.2890del (p.Gln964fs) rs886042168
NM_000833.5(GRIN2A):c.3813G>A (p.Trp1271Ter) rs886043129
NM_000833.5(GRIN2A):c.627del (p.Phe210fs) rs796052560
NM_001134407.3(GRIN2A):c.1007+1G>A rs397518465
NM_001134407.3(GRIN2A):c.1553G>A (p.Arg518His) rs397518470
NM_001134407.3(GRIN2A):c.3701del (p.Phe1234fs) rs886041308
NM_001134407.3(GRIN2A):c.487C>T (p.Gln163Ter) rs1057524089

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.