ClinVar Miner

List of variants in gene GRM1 reported as benign by Athena Diagnostics Inc

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 30
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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.3357G>C (p.Thr1119=) rs1047008 0.03250
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.624C>T (p.Asp208=) rs112670841 0.00395
NM_001278064.2(GRM1):c.3206C>T (p.Pro1069Leu) rs79336287 0.00337
NM_001278064.2(GRM1):c.1980G>A (p.Gln660=) rs138840977 0.00289
NM_001278064.2(GRM1):c.2043T>C (p.Arg681=) rs143682838 0.00289
NM_001278064.2(GRM1):c.2496T>C (p.Thr832=) rs142675468 0.00288
NM_001278064.2(GRM1):c.922G>A (p.Val308Ile) rs112915383 0.00277
NM_001278064.2(GRM1):c.3219G>A (p.Gln1073=) rs362826 0.00267
NM_001278064.2(GRM1):c.1186+10G>A rs142233320 0.00192
NM_001278064.2(GRM1):c.3161G>A (p.Gly1054Asp) rs145764886 0.00188
NM_001278064.2(GRM1):c.408G>A (p.Gly136=) rs151118347 0.00168
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.1338C>T (p.Asp446=) rs142264383 0.00036
NM_001278064.2(GRM1):c.774T>G (p.Ser258=) rs183502505 0.00014
NM_001278064.2(GRM1):c.3381G>A (p.Glu1127=) rs77895673 0.00001
NM_001278064.2(GRM1):c.2007G>T (p.Ala669=) rs148926588
NM_001278064.2(GRM1):c.2364G>C (p.Ala788=) rs114187147
NM_001278064.2(GRM1):c.3213T>C (p.Pro1071=) rs1047006

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