ClinVar Miner

Variants in gene GRM1 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 27
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001278064.2(GRM1):c.3168T>G (p.Gly1056=) rs6923864 0.64620
NM_001278064.2(GRM1):c.2977T>C (p.Ser993Pro) rs6923492 0.56892
NM_001278064.2(GRM1):c.3495C>A (p.Pro1165=) rs9373491 0.55222
NM_001278064.2(GRM1):c.2793G>A (p.Lys931=) rs2942 0.49950
NM_001278064.2(GRM1):c.2651G>A (p.Gly884Glu) rs362936 0.01411
NM_001278064.2(GRM1):c.2185C>A (p.Pro729Thr) rs41305288 0.01244
NM_001278064.2(GRM1):c.2785G>A (p.Val929Ile) rs2941 0.01171
NM_001278064.2(GRM1):c.3107G>T (p.Gly1036Val) rs144944927 0.00751
NM_001278064.2(GRM1):c.3214C>G (p.Pro1072Ala) rs146753539 0.00646
NM_001278064.2(GRM1):c.3206C>T (p.Pro1069Leu) rs79336287 0.00337
NM_001278064.2(GRM1):c.922G>A (p.Val308Ile) rs112915383 0.00277
NM_001278064.2(GRM1):c.2859C>T (p.Thr953=) rs116471335 0.00249
NM_001278064.2(GRM1):c.3161G>A (p.Gly1054Asp) rs145764886 0.00188
NM_001278064.2(GRM1):c.2991A>G (p.Ala997=) rs140244084 0.00118
NM_001278064.2(GRM1):c.1433+10T>C rs373538200 0.00111
NM_001278064.2(GRM1):c.444C>G (p.Pro148=) rs138794480 0.00071
NM_001278064.2(GRM1):c.2922T>C (p.Pro974=) rs142409803 0.00065
NM_001278064.2(GRM1):c.2581G>A (p.Gly861Ser) rs143544032 0.00056
NM_001278064.2(GRM1):c.3381G>A (p.Glu1127=) rs77895673 0.00001
NM_001278064.2(GRM1):c.3213T>C (p.Pro1071=) rs1047006
NM_001278064.2(GRM1):c.3213T>G (p.Pro1071=) rs1047006
NM_001278064.2(GRM1):c.669T>C (p.Asn223=)
NM_001278064.2(GRM1):c.950+8TC[14] rs72225459
NM_001278064.2(GRM1):c.950+8TC[17] rs72225459
NM_001278064.2(GRM1):c.950+8TC[18] rs72225459
NM_001278064.2(GRM1):c.950+8TC[20] rs72225459
NM_001278064.2(GRM1):c.950+8TC[21] rs72225459

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.