ClinVar Miner

List of variants in gene GRM6, LOC100130798 studied for congenital stationary night blindness 1B

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
Download table as spreadsheet
NM_000843.4(GRM6):c.1214T>C (p.Ile405Thr) rs121434304
NM_000843.4(GRM6):c.1307C>T (p.Thr436Ile) rs5019554
NM_000843.4(GRM6):c.1533C>T (p.His511=) rs61733043
NM_000843.4(GRM6):c.1537G>A (p.Val513Met) rs201396068
NM_000843.4(GRM6):c.1565G>A (p.Cys522Tyr) rs62638208
NM_000843.4(GRM6):c.1861C>T (p.Arg621Ter) rs62638214
NM_000843.4(GRM6):c.1875C>T (p.Tyr625=) rs62638215
NM_000843.4(GRM6):c.2122C>T (p.Gln708Ter) rs62638624
NM_000843.4(GRM6):c.2240C>T (p.Ser747Leu)
NM_000843.4(GRM6):c.2341G>A (p.Glu781Lys) rs62638625

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.