ClinVar Miner

List of variants in gene GRM7 reported as benign for not provided

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Gene type:
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Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_000844.4(GRM7):c.519+7A>G rs342034 0.96701
NM_000844.4(GRM7):c.2196T>C (p.Tyr732=) rs1485175 0.56650
NM_000844.4(GRM7):c.222C>T (p.Asn74=) rs3749380 0.36532
NM_000844.4(GRM7):c.1298A>T (p.Tyr433Phe) rs2229902 0.30241
NM_000844.4(GRM7):c.1789C>T (p.Leu597=) rs7614915 0.22935
NM_000844.4(GRM7):c.1575A>G (p.Leu525=) rs34373930 0.22930
NM_000844.4(GRM7):c.2235G>A (p.Gly745=) rs1485174 0.22896
NM_000844.4(GRM7):c.2698+15G>A rs2280739 0.12508
NM_000844.4(GRM7):c.99C>A (p.Arg33=) rs116111799 0.01523
NM_000844.4(GRM7):c.1750C>T (p.Leu584=) rs80099685 0.01399
NM_000844.4(GRM7):c.561T>C (p.Ser187=) rs35106713 0.00872
NM_000844.4(GRM7):c.2439A>G (p.Gln813=) rs76544064 0.00764
NM_000844.4(GRM7):c.552C>A (p.Pro184=) rs139429824 0.00484
NM_000844.4(GRM7):c.1179G>A (p.Gln393=) rs34067965 0.00405
NM_000844.4(GRM7):c.81G>C (p.Ala27=) rs138762445 0.00300
NM_000844.4(GRM7):c.114C>T (p.Tyr38=) rs114869468 0.00169
NM_000844.4(GRM7):c.144C>T (p.Asp48=) rs142650646 0.00153
NM_000844.4(GRM7):c.1854G>A (p.Thr618=) rs146236743 0.00077
NM_000844.4(GRM7):c.1356A>C (p.Ile452=) rs138874035 0.00072
NM_000844.4(GRM7):c.1026G>A (p.Thr342=) rs78137319 0.00044
NM_000844.4(GRM7):c.759C>T (p.Ser253=) rs144380165 0.00041
NM_000844.4(GRM7):c.2388G>A (p.Thr796=) rs117160055 0.00020
NM_000844.4(GRM7):c.2655C>T (p.Asn885=) rs546761323 0.00006
NM_000844.4(GRM7):c.2577G>C (p.Arg859=) rs201806420 0.00004
NM_000844.4(GRM7):c.67G>A (p.Val23Met) rs535666333 0.00001
NM_000844.4(GRM7):c.1175-48TG[16]
NM_000844.4(GRM7):c.1300C>A (p.Arg434=)
NM_000844.4(GRM7):c.300G>T (p.Thr100=)

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