ClinVar Miner

List of variants in gene GRM1 reported by Athena Diagnostics Inc

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Gene type:
ClinVar version:
Total variants: 99
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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.2859C>T (p.Thr953=) rs116471335 0.00249
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.2340C>T (p.Asn780=) rs41285861 0.00031
NM_001278064.2(GRM1):c.1073G>A (p.Arg358Lys) rs112817798 0.00024
NM_001278064.2(GRM1):c.1372T>G (p.Ser458Ala) rs151255685 0.00021
NM_001278064.2(GRM1):c.2725A>C (p.Met909Leu) rs138759146 0.00020
NM_001278064.2(GRM1):c.1488C>T (p.His496=) rs141568265 0.00018
NM_001278064.2(GRM1):c.1689A>C (p.Lys563Asn) rs372316073 0.00017
NM_001278064.2(GRM1):c.3426G>T (p.Ser1142=) rs147521426 0.00017
NM_001278064.2(GRM1):c.2265C>A (p.Ala755=) rs150675631 0.00014
NM_001278064.2(GRM1):c.774T>G (p.Ser258=) rs183502505 0.00014
NM_001278064.2(GRM1):c.1773C>T (p.Ile591=) rs138083268 0.00011
NM_001278064.2(GRM1):c.1750C>T (p.Arg584Cys) rs146996893 0.00010
NM_001278064.2(GRM1):c.2661-7309A>T rs768023437 0.00010
NM_001278064.2(GRM1):c.3328G>A (p.Val1110Met) rs373321710 0.00010
NM_001278064.2(GRM1):c.1643C>T (p.Thr548Met) rs201399008 0.00009
NM_001278064.2(GRM1):c.1982G>A (p.Arg661His) rs200495057 0.00009
NM_001278064.2(GRM1):c.3000C>T (p.Thr1000=) rs746188712 0.00008
NM_001278064.2(GRM1):c.1524T>C (p.Asp508=) rs368772965 0.00006
NM_001278064.2(GRM1):c.827A>C (p.Lys276Thr) rs192397712 0.00006
NM_001278064.2(GRM1):c.3044C>G (p.Pro1015Arg) rs199777173 0.00005
NM_001278064.2(GRM1):c.1422C>T (p.Asp474=) rs371221115 0.00004
NM_001278064.2(GRM1):c.3339C>T (p.His1113=) rs754649454 0.00004
NM_001278064.2(GRM1):c.2026G>A (p.Val676Met) rs752403373 0.00003
NM_001278064.2(GRM1):c.2909C>T (p.Pro970Leu) rs1432380664 0.00003
NM_001278064.2(GRM1):c.3554G>A (p.Arg1185Gln) rs557752501 0.00003
NM_001278064.2(GRM1):c.1494A>G (p.Gly498=) rs767873257 0.00002
NM_001278064.2(GRM1):c.113T>C (p.Val38Ala) rs374907798 0.00001
NM_001278064.2(GRM1):c.1754A>G (p.Tyr585Cys) rs754787480 0.00001
NM_001278064.2(GRM1):c.2062G>A (p.Gly688Ser) rs965990929 0.00001
NM_001278064.2(GRM1):c.2087G>A (p.Arg696Gln) rs746003735 0.00001
NM_001278064.2(GRM1):c.2252T>A (p.Leu751Gln) rs767615613 0.00001
NM_001278064.2(GRM1):c.3381G>A (p.Glu1127=) rs77895673 0.00001
NM_001278064.2(GRM1):c.33G>C (p.Ala11=) rs199734282 0.00001
NM_001278064.2(GRM1):c.3408A>G (p.Lys1136=) rs1040774327 0.00001
NM_001278064.2(GRM1):c.41T>G (p.Leu14Trp) rs774851565 0.00001
NM_001278064.2(GRM1):c.50C>T (p.Ser17Phe) rs1477880063 0.00001
NM_001278064.2(GRM1):c.722T>C (p.Met241Thr) rs768616151 0.00001
NM_001278064.2(GRM1):c.1137C>T (p.Arg379=) rs1783517255
NM_001278064.2(GRM1):c.1156G>C (p.Glu386Gln)
NM_001278064.2(GRM1):c.1201G>A (p.Glu401Lys)
NM_001278064.2(GRM1):c.1524T>G (p.Asp508Glu) rs368772965
NM_001278064.2(GRM1):c.1603-9A>G rs1394609987
NM_001278064.2(GRM1):c.1723C>G (p.Leu575Val) rs1193170688
NM_001278064.2(GRM1):c.2000C>T (p.Ser667Phe)
NM_001278064.2(GRM1):c.2007G>T (p.Ala669=) rs148926588
NM_001278064.2(GRM1):c.2252T>C (p.Leu751Pro)
NM_001278064.2(GRM1):c.2364G>C (p.Ala788=) rs114187147
NM_001278064.2(GRM1):c.2661-7270G>A rs1778221372
NM_001278064.2(GRM1):c.2661-7293C>T
NM_001278064.2(GRM1):c.2766G>C (p.Thr922=) rs557241976
NM_001278064.2(GRM1):c.2860C>T (p.Leu954Phe) rs1583494926
NM_001278064.2(GRM1):c.2944G>A (p.Val982Met) rs867889855
NM_001278064.2(GRM1):c.2962A>G (p.Thr988Ala) rs1583495145
NM_001278064.2(GRM1):c.3039G>T (p.Leu1013Phe)
NM_001278064.2(GRM1):c.3138G>A (p.Pro1046=)
NM_001278064.2(GRM1):c.3155T>A (p.Leu1052Gln) rs1268764914
NM_001278064.2(GRM1):c.3178A>G (p.Asn1060Asp) rs755308114
NM_001278064.2(GRM1):c.3181G>C (p.Gly1061Arg)
NM_001278064.2(GRM1):c.3194_3199dup (p.Leu1065_Tyr1066dup) rs774663606
NM_001278064.2(GRM1):c.3202C>T (p.Pro1068Ser)
NM_001278064.2(GRM1):c.3207G>A (p.Pro1069=)
NM_001278064.2(GRM1):c.3212C>G (p.Pro1071Arg) rs149072960
NM_001278064.2(GRM1):c.3213T>C (p.Pro1071=) rs1047006
NM_001278064.2(GRM1):c.3245T>C (p.Leu1082Pro)
NM_001278064.2(GRM1):c.3283GAC[6] (p.Asp1099dup) rs750936487
NM_001278064.2(GRM1):c.32C>G (p.Ala11Gly)
NM_001278064.2(GRM1):c.3341A>T (p.Glu1114Val)
NM_001278064.2(GRM1):c.3366C>A (p.Asp1122Glu)
NM_001278064.2(GRM1):c.3456C>T (p.Arg1152=)
NM_001278064.2(GRM1):c.3524C>T (p.Pro1175Leu)
NM_001278064.2(GRM1):c.428A>T (p.Asp143Val) rs766288983
NM_001278064.2(GRM1):c.457A>G (p.Lys153Glu)
NM_001278064.2(GRM1):c.829C>A (p.Leu277Ile) rs1022097029
NM_001278064.2(GRM1):c.885A>C (p.Thr295=)

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