ClinVar Miner

List of variants in gene GRM6 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 113
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HGVS dbSNP gnomAD frequency
NM_000843.4(GRM6):c.504+66A>C rs62638203 0.02083
NM_000843.4(GRM6):c.19G>A (p.Ala7Thr) rs62642053 0.00533
NM_000843.4(GRM6):c.177G>A (p.Gln59=) rs563976478 0.00094
NM_000843.4(GRM6):c.415C>A (p.Pro139Thr) rs971140136 0.00051
NM_000843.4(GRM6):c.721+12G>T rs201103197 0.00050
NM_000843.4(GRM6):c.621C>T (p.Ile207=) rs75666388 0.00049
NM_000843.4(GRM6):c.261C>T (p.Pro87=) rs62638199 0.00032
NM_000843.4(GRM6):c.465C>T (p.Ser155=) rs560013977 0.00029
NM_000843.4(GRM6):c.404C>G (p.Pro135Arg) rs1034464770 0.00025
NM_000843.4(GRM6):c.111C>A (p.Gly37=) rs1076877 0.00019
NM_000843.4(GRM6):c.96T>C (p.Ser32=) rs967626699 0.00015
NM_000843.4(GRM6):c.222C>T (p.Tyr74=) rs778393434 0.00008
NM_000843.4(GRM6):c.588C>T (p.Pro196=) rs756171835 0.00008
NM_000843.4(GRM6):c.699C>T (p.Phe233=) rs367700792 0.00008
NM_000843.4(GRM6):c.315G>A (p.Ala105=) rs748710923 0.00007
NM_000843.4(GRM6):c.459C>T (p.Ala153=) rs1428570845 0.00007
NM_000843.4(GRM6):c.306C>T (p.Asp102=) rs769977682 0.00006
NM_000843.4(GRM6):c.36C>T (p.Leu12=) rs1289302384 0.00006
NM_000843.4(GRM6):c.354C>A (p.Arg118=) rs763774664 0.00005
NM_000843.4(GRM6):c.505-9G>A rs377001985 0.00005
NM_000843.4(GRM6):c.537G>A (p.Pro179=) rs771271291 0.00005
NM_000843.4(GRM6):c.31C>T (p.Leu11=) rs986210410 0.00004
NM_000843.4(GRM6):c.357C>T (p.Gly119=) rs747289985 0.00004
NM_000843.4(GRM6):c.546C>T (p.Ser182=) rs200220261 0.00004
NM_000843.4(GRM6):c.678C>T (p.Gly226=) rs376072998 0.00004
NM_000843.4(GRM6):c.732T>C (p.Cys244=) rs777695214 0.00004
NM_000843.4(GRM6):c.857+11G>A rs373231647 0.00004
NM_000843.4(GRM6):c.663C>T (p.Ser221=) rs752901391 0.00003
NM_000843.4(GRM6):c.963C>T (p.Asp321=) rs201148002 0.00003
NM_000843.4(GRM6):c.153C>T (p.Gly51=) rs1399732883 0.00002
NM_000843.4(GRM6):c.654G>A (p.Thr218=) rs756422865 0.00002
NM_000843.4(GRM6):c.721+17G>A rs368697449 0.00002
NM_000843.4(GRM6):c.722-6G>A rs759736998 0.00002
NM_000843.4(GRM6):c.722-7C>T rs201778316 0.00002
NM_000843.4(GRM6):c.822G>T (p.Arg274=) rs769329232 0.00002
NM_000843.4(GRM6):c.159G>A (p.Ala53=) rs1451403635 0.00001
NM_000843.4(GRM6):c.249C>G (p.Pro83=) rs752617366 0.00001
NM_000843.4(GRM6):c.312C>T (p.Tyr104=) rs1317273313 0.00001
NM_000843.4(GRM6):c.327G>T (p.Ala109=) rs781517298 0.00001
NM_000843.4(GRM6):c.33G>A (p.Leu11=) rs1285317329 0.00001
NM_000843.4(GRM6):c.342G>A (p.Gln114=) rs1238369993 0.00001
NM_000843.4(GRM6):c.366C>T (p.Asp122=) rs1193779719 0.00001
NM_000843.4(GRM6):c.387C>G (p.Arg129=) rs1760738194 0.00001
NM_000843.4(GRM6):c.486C>T (p.Asn162=) rs1204290337 0.00001
NM_000843.4(GRM6):c.51G>T (p.Pro17=) rs763973168 0.00001
NM_000843.4(GRM6):c.603G>A (p.Ala201=) rs766764983 0.00001
NM_000843.4(GRM6):c.645T>C (p.Tyr215=) rs770664445 0.00001
NM_000843.4(GRM6):c.69G>A (p.Gln23=) rs954810080 0.00001
NM_000843.4(GRM6):c.722-19T>G rs763971027 0.00001
NM_000843.4(GRM6):c.723G>T (p.Gly241=) rs773866005 0.00001
NM_000843.4(GRM6):c.753T>C (p.Ile251=) rs377710656 0.00001
NM_000843.4(GRM6):c.816C>T (p.Asn272=) rs1046529474 0.00001
NM_000843.4(GRM6):c.831C>T (p.Ile277=) rs1448056585 0.00001
NM_000843.4(GRM6):c.858-15C>A rs1272430470 0.00001
NM_000843.4(GRM6):c.858-5A>G rs773739046 0.00001
NM_000843.4(GRM6):c.894C>T (p.Thr298=) rs199833388 0.00001
NM_000843.4(GRM6):c.912C>T (p.Val304=) rs1008360422 0.00001
NM_000843.4(GRM6):c.957G>A (p.Leu319=) rs1412869397 0.00001
NM_000843.4(GRM6):c.966G>A (p.Val322=) rs1322838658 0.00001
NM_000843.4(GRM6):c.969C>T (p.Ala323=) rs777884872 0.00001
NM_000843.4(GRM6):c.975G>A (p.Gly325=) rs528831135 0.00001
NM_000843.4(GRM6):c.1008C>A (p.Ile336=) rs138201914
NM_000843.4(GRM6):c.1008C>T (p.Ile336=) rs138201914
NM_000843.4(GRM6):c.1012+12G>A
NM_000843.4(GRM6):c.1012+7C>T rs2480393946
NM_000843.4(GRM6):c.120G>T (p.Thr40=) rs2480408553
NM_000843.4(GRM6):c.135C>T (p.Phe45=) rs958864799
NM_000843.4(GRM6):c.144C>T (p.His48=)
NM_000843.4(GRM6):c.150G>A (p.Arg50=) rs1760744489
NM_000843.4(GRM6):c.162C>A (p.Gly54=) rs1441068298
NM_000843.4(GRM6):c.176_177delinsCA (p.Gln59Pro) rs2113348250
NM_000843.4(GRM6):c.225G>C (p.Ala75=) rs2113348101
NM_000843.4(GRM6):c.246C>T (p.Asp82=) rs753291673
NM_000843.4(GRM6):c.294C>A (p.Thr98=) rs2480407830
NM_000843.4(GRM6):c.300G>A (p.Ser100=)
NM_000843.4(GRM6):c.316C>T (p.Leu106=) rs1760739936
NM_000843.4(GRM6):c.336C>T (p.Phe112=) rs62638200
NM_000843.4(GRM6):c.393G>C (p.Pro131=) rs958979347
NM_000843.4(GRM6):c.409C>T (p.Leu137=) rs2113347613
NM_000843.4(GRM6):c.411G>A (p.Leu137=)
NM_000843.4(GRM6):c.483C>A (p.Ala161=)
NM_000843.4(GRM6):c.489G>T (p.Val163=)
NM_000843.4(GRM6):c.48G>A (p.Leu16=) rs2480408867
NM_000843.4(GRM6):c.492G>A (p.Leu164=) rs2480407097
NM_000843.4(GRM6):c.504+18G>T rs1299442483
NM_000843.4(GRM6):c.504+20G>A rs572890701
NM_000843.4(GRM6):c.504+20del rs561067511
NM_000843.4(GRM6):c.504+9C>T rs1356451738
NM_000843.4(GRM6):c.505-12C>A
NM_000843.4(GRM6):c.52C>T (p.Leu18=) rs1390795419
NM_000843.4(GRM6):c.579G>A (p.Val193=) rs1274655234
NM_000843.4(GRM6):c.579G>C (p.Val193=) rs1274655234
NM_000843.4(GRM6):c.588C>A (p.Pro196=) rs756171835
NM_000843.4(GRM6):c.58_72del (p.Trp20_Ala24del) rs1189206125
NM_000843.4(GRM6):c.621C>A (p.Ile207=) rs75666388
NM_000843.4(GRM6):c.633G>A (p.Leu211=)
NM_000843.4(GRM6):c.660C>A (p.Ala220=) rs2113343261
NM_000843.4(GRM6):c.675T>C (p.Tyr225=) rs2480400229
NM_000843.4(GRM6):c.687G>A (p.Gly229=)
NM_000843.4(GRM6):c.68_82del (p.Gln23_Ala27del) rs757326094
NM_000843.4(GRM6):c.721+16C>G rs3733913
NM_000843.4(GRM6):c.721+16C>T rs3733913
NM_000843.4(GRM6):c.722-13C>A rs2113342347
NM_000843.4(GRM6):c.726G>C (p.Gly242=) rs564369800
NM_000843.4(GRM6):c.727G>T (p.Val243Phe) rs17078894
NM_000843.4(GRM6):c.795G>A (p.Arg265=) rs2480398603
NM_000843.4(GRM6):c.857+10T>C rs2113341931
NM_000843.4(GRM6):c.857+12G>C rs754325926
NM_000843.4(GRM6):c.857+12G>T rs754325926
NM_000843.4(GRM6):c.858-4C>T rs1360586921
NM_000843.4(GRM6):c.858-5A>T rs773739046
NM_000843.4(GRM6):c.867G>T (p.Leu289=) rs1760654899
NM_000843.4(GRM6):c.894C>A (p.Thr298=) rs199833388

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