ClinVar Miner

List of variants in gene GRM1 reported as uncertain significance by GeneDx

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Gene type:
ClinVar version:
Total variants: 29
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HGVS dbSNP gnomAD frequency
NM_001278064.2(GRM1):c.2581G>A (p.Gly861Ser) rs143544032 0.00056
NM_001278064.2(GRM1):c.1689A>C (p.Lys563Asn) rs372316073 0.00017
NM_001278064.2(GRM1):c.1603G>A (p.Val535Ile) rs370801324 0.00005
NM_001278064.2(GRM1):c.2818T>A (p.Ser940Thr) rs559782958 0.00004
NM_001278064.2(GRM1):c.1666G>A (p.Val556Met) rs761933016 0.00003
NM_001278064.2(GRM1):c.2215A>G (p.Ile739Val) rs578089091 0.00003
NM_001278064.2(GRM1):c.2006C>T (p.Ala669Val) rs776187845 0.00001
NM_001278064.2(GRM1):c.1453C>A (p.Gln485Lys) rs2115053962
NM_001278064.2(GRM1):c.1691C>T (p.Ala564Val)
NM_001278064.2(GRM1):c.1730G>T (p.Gly577Val) rs1320752335
NM_001278064.2(GRM1):c.2017T>C (p.Ser673Pro)
NM_001278064.2(GRM1):c.212G>C (p.Arg71Thr) rs2128834249
NM_001278064.2(GRM1):c.2228A>G (p.Tyr743Cys) rs2483999164
NM_001278064.2(GRM1):c.224G>A (p.Gly75Asp) rs2482536335
NM_001278064.2(GRM1):c.2509A>C (p.Ile837Leu) rs1432798773
NM_001278064.2(GRM1):c.2539C>T (p.Arg847Cys)
NM_001278064.2(GRM1):c.2570G>A (p.Arg857His)
NM_001278064.2(GRM1):c.2641G>A (p.Ala881Thr) rs2114585265
NM_001278064.2(GRM1):c.2669G>C (p.Gly890Ala) rs2484160253
NM_001278064.2(GRM1):c.2726T>C (p.Met909Thr) rs141525895
NM_001278064.2(GRM1):c.3031A>G (p.Lys1011Glu) rs2484163670
NM_001278064.2(GRM1):c.3095A>T (p.Asp1032Val) rs2484164271
NM_001278064.2(GRM1):c.3121_3124dup (p.Ser1042fs) rs2114699585
NM_001278064.2(GRM1):c.3149C>T (p.Ala1050Val)
NM_001278064.2(GRM1):c.3364G>A (p.Asp1122Asn) rs1778532092
NM_001278064.2(GRM1):c.3425C>T (p.Ser1142Leu) rs917848032
NM_001278064.2(GRM1):c.3479C>G (p.Ser1160Trp) rs1778538011
NM_001278064.2(GRM1):c.3505_3507del (p.Ser1169del)
NM_001278064.2(GRM1):c.745G>T (p.Ala249Ser)

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