ClinVar Miner

List of variants in gene GRM4 reported as uncertain significance by Ambry Genetics

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Gene type:
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Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_000841.4(GRM4):c.1712C>T (p.Thr571Met) rs573897815 0.00009
NM_000841.4(GRM4):c.823A>G (p.Thr275Ala) rs373483140 0.00009
NM_000841.4(GRM4):c.1550G>A (p.Arg517His) rs559913506 0.00007
NM_000841.4(GRM4):c.1840G>A (p.Asp614Asn) rs372962596 0.00007
NM_000841.4(GRM4):c.1942G>A (p.Asp648Asn) rs150458970 0.00007
NM_000841.4(GRM4):c.1294G>A (p.Val432Met) rs566158040 0.00005
NM_000841.4(GRM4):c.2456C>T (p.Thr819Met) rs754789724 0.00005
NM_000841.4(GRM4):c.2506A>G (p.Met836Val) rs139612028 0.00005
NM_000841.4(GRM4):c.409G>A (p.Gly137Ser) rs943020473 0.00005
NM_000841.4(GRM4):c.2429A>G (p.Gln810Arg) rs746461387 0.00004
NM_000841.4(GRM4):c.1397A>G (p.Asn466Ser) rs776152688 0.00003
NM_000841.4(GRM4):c.696G>C (p.Glu232Asp) rs375096027 0.00003
NM_000841.4(GRM4):c.1172G>A (p.Arg391His) rs374647710 0.00002
NM_000841.4(GRM4):c.1660C>T (p.Arg554Cys) rs750227583 0.00001
NM_000841.4(GRM4):c.1832G>A (p.Arg611His) rs375967226 0.00001
NM_000841.4(GRM4):c.2345A>G (p.Asn782Ser) rs779540722 0.00001
NM_000841.4(GRM4):c.2459C>T (p.Thr820Met) rs571074814 0.00001
NM_000841.4(GRM4):c.2671G>C (p.Glu891Gln) rs768993231 0.00001
NM_000841.4(GRM4):c.2684C>T (p.Ala895Val) rs767070176 0.00001
NM_000841.4(GRM4):c.2690C>T (p.Ala897Val) rs1048408205 0.00001
NM_000841.4(GRM4):c.620A>G (p.Gln207Arg) rs1439703735 0.00001
NM_000841.4(GRM4):c.689A>G (p.Tyr230Cys) rs928835239 0.00001
NM_000841.4(GRM4):c.100C>T (p.Pro34Ser) rs2532509175
NM_000841.4(GRM4):c.1033G>A (p.Asp345Asn)
NM_000841.4(GRM4):c.113C>T (p.Pro38Leu)
NM_000841.4(GRM4):c.1195G>A (p.Ala399Thr)
NM_000841.4(GRM4):c.1223T>C (p.Phe408Ser)
NM_000841.4(GRM4):c.1230C>G (p.Ile410Met) rs144608064
NM_000841.4(GRM4):c.1264G>A (p.Ala422Thr)
NM_000841.4(GRM4):c.1309C>T (p.Arg437Cys)
NM_000841.4(GRM4):c.1418G>A (p.Gly473Glu)
NM_000841.4(GRM4):c.1441C>A (p.Gln481Lys)
NM_000841.4(GRM4):c.1538A>C (p.Gln513Pro) rs1342392985
NM_000841.4(GRM4):c.1549C>T (p.Arg517Cys)
NM_000841.4(GRM4):c.1627G>A (p.Glu543Lys)
NM_000841.4(GRM4):c.1730C>T (p.Pro577Leu)
NM_000841.4(GRM4):c.1839C>A (p.Asn613Lys) rs137929521
NM_000841.4(GRM4):c.1931T>C (p.Ile644Thr) rs773619608
NM_000841.4(GRM4):c.1961T>C (p.Leu654Pro)
NM_000841.4(GRM4):c.2027G>A (p.Arg676His)
NM_000841.4(GRM4):c.203G>T (p.Gly68Val) rs755882469
NM_000841.4(GRM4):c.2255C>T (p.Ser752Leu)
NM_000841.4(GRM4):c.2324G>A (p.Arg775His)
NM_000841.4(GRM4):c.232C>T (p.Arg78Trp)
NM_000841.4(GRM4):c.2508G>A (p.Met836Ile)
NM_000841.4(GRM4):c.2566C>T (p.Arg856Cys)
NM_000841.4(GRM4):c.2573G>A (p.Arg858His)
NM_000841.4(GRM4):c.263G>T (p.Arg88Leu) rs764896879
NM_000841.4(GRM4):c.2713G>A (p.Val905Ile)
NM_000841.4(GRM4):c.271A>C (p.Asn91His) rs2532508576
NM_000841.4(GRM4):c.29G>T (p.Trp10Leu)
NM_000841.4(GRM4):c.419G>A (p.Gly140Asp)
NM_000841.4(GRM4):c.508C>T (p.Arg170Cys)
NM_000841.4(GRM4):c.509G>A (p.Arg170His)
NM_000841.4(GRM4):c.592G>C (p.Val198Leu)
NM_000841.4(GRM4):c.608C>T (p.Thr203Met) rs2533918920
NM_000841.4(GRM4):c.683G>A (p.Gly228Asp)
NM_000841.4(GRM4):c.708G>T (p.Glu236Asp) rs2533918213
NM_000841.4(GRM4):c.758C>T (p.Ser253Leu)
NM_000841.4(GRM4):c.772C>T (p.Arg258Trp) rs572550212
NM_000841.4(GRM4):c.809G>T (p.Arg270Leu)
NM_000841.4(GRM4):c.81G>A (p.Met27Ile)
NM_000841.4(GRM4):c.874C>T (p.Arg292Cys)
NM_000841.4(GRM4):c.908C>T (p.Thr303Ile)
NM_000841.4(GRM4):c.913C>T (p.His305Tyr) rs2533770229
NM_000841.4(GRM4):c.967C>T (p.His323Tyr) rs937880546

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