ClinVar Miner

List of variants in gene GRIN2A reported as likely benign by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 77
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HGVS dbSNP gnomAD frequency
NM_001134407.3(GRIN2A):c.2899G>C (p.Val967Leu) rs61731465 0.00502
NM_001134407.3(GRIN2A):c.3228C>A (p.Asn1076Lys) rs61758995 0.00472
NM_001134407.3(GRIN2A):c.662A>G (p.Lys221Arg) rs61731464 0.00322
NM_001134407.3(GRIN2A):c.1251C>T (p.Val417=) rs139329447 0.00150
NM_001134407.3(GRIN2A):c.900C>T (p.Thr300=) rs143669998 0.00133
NM_001134407.3(GRIN2A):c.903C>T (p.Thr301=) rs78241448 0.00119
NM_001134407.3(GRIN2A):c.669C>T (p.His223=) rs138117658 0.00076
NM_001134407.3(GRIN2A):c.3827C>G (p.Ala1276Gly) rs145063086 0.00067
NM_001134407.3(GRIN2A):c.2883C>T (p.Asn961=) rs77705198 0.00059
NM_001134407.3(GRIN2A):c.3190A>G (p.Thr1064Ala) rs138809301 0.00055
NM_001134407.3(GRIN2A):c.666C>T (p.Ile222=) rs143594020 0.00039
NM_001134407.3(GRIN2A):c.741C>T (p.Gly247=) rs141912603 0.00039
NM_001134407.3(GRIN2A):c.942C>T (p.Pro314=) rs145172949 0.00031
NM_001134407.3(GRIN2A):c.939C>T (p.Ile313=) rs146867324 0.00030
NM_001134407.3(GRIN2A):c.1410T>G (p.Thr470=) rs372058698 0.00028
NM_001134407.3(GRIN2A):c.2165C>T (p.Thr722Met) rs376029542 0.00024
NM_001134407.3(GRIN2A):c.2202C>G (p.Val734=) rs367543138 0.00023
NM_001134407.3(GRIN2A):c.1458C>A (p.Gly486=) rs144572467 0.00019
NM_001134407.3(GRIN2A):c.1155G>C (p.Leu385=) rs139119497 0.00015
NM_001134407.3(GRIN2A):c.963C>T (p.Tyr321=) rs368200727 0.00014
NM_001134407.3(GRIN2A):c.819A>G (p.Pro273=) rs148085725 0.00013
NM_001134407.3(GRIN2A):c.4356C>G (p.Arg1452=) rs140093291 0.00012
NM_001134407.3(GRIN2A):c.447G>A (p.Ala149=) rs144464666 0.00009
NM_001134407.3(GRIN2A):c.1533G>A (p.Ser511=) rs112848130 0.00007
NM_001134407.3(GRIN2A):c.3898A>G (p.Arg1300Gly) rs372353067 0.00007
NM_001134407.3(GRIN2A):c.419C>T (p.Pro140Leu) rs142566406 0.00007
NM_001134407.3(GRIN2A):c.1141C>T (p.His381Tyr) rs757464009 0.00006
NM_001134407.3(GRIN2A):c.1164C>T (p.Ala388=) rs151137679 0.00006
NM_001134407.3(GRIN2A):c.2250C>T (p.Ile750=) rs143779792 0.00006
NM_001134407.3(GRIN2A):c.2760A>G (p.Arg920=) rs80138441 0.00006
NM_001134407.3(GRIN2A):c.2909G>A (p.Arg970Gln) rs148669437 0.00006
NM_001134407.3(GRIN2A):c.559G>A (p.Val187Ile) rs751692867 0.00006
NM_001134407.3(GRIN2A):c.623C>T (p.Thr208Ile) rs367543124 0.00006
NM_001134407.3(GRIN2A):c.2811T>A (p.Asp937Glu) rs570907044 0.00005
NM_001134407.3(GRIN2A):c.2966A>G (p.Asn989Ser) rs531782747 0.00005
NM_001134407.3(GRIN2A):c.567C>A (p.Thr189=) rs758864728 0.00005
NM_001134407.3(GRIN2A):c.1119A>G (p.Glu373=) rs368406915 0.00004
NM_001134407.3(GRIN2A):c.2664G>A (p.Thr888=) rs113847665 0.00004
NM_001134407.3(GRIN2A):c.3366T>G (p.Gly1122=) rs1060504864 0.00004
NM_001134407.3(GRIN2A):c.3051C>T (p.Ser1017=) rs773366584 0.00003
NM_001134407.3(GRIN2A):c.3426C>T (p.Pro1142=) rs150487431 0.00003
NM_001134407.3(GRIN2A):c.3578T>G (p.Leu1193Trp) rs75761674 0.00003
NM_001134407.3(GRIN2A):c.4205G>A (p.Arg1402Gln) rs74935155 0.00003
NM_001134407.3(GRIN2A):c.1201C>G (p.Pro401Ala) rs762535029 0.00002
NM_001134407.3(GRIN2A):c.2652C>T (p.Asp884=) rs755207993 0.00002
NM_001134407.3(GRIN2A):c.3028C>A (p.Pro1010Thr) rs753651908 0.00002
NM_001134407.3(GRIN2A):c.91C>T (p.Pro31Ser) rs199942034 0.00002
NM_001134407.3(GRIN2A):c.1437G>A (p.Leu479=) rs768988228 0.00001
NM_001134407.3(GRIN2A):c.2238G>A (p.Lys746=) rs1473479428 0.00001
NM_001134407.3(GRIN2A):c.2681T>A (p.Met894Lys) rs775144380 0.00001
NM_001134407.3(GRIN2A):c.2809G>A (p.Asp937Asn) rs769602505 0.00001
NM_001134407.3(GRIN2A):c.2927A>G (p.Asn976Ser) rs886039239 0.00001
NM_001134407.3(GRIN2A):c.3118G>A (p.Glu1040Lys) rs778490114 0.00001
NM_001134407.3(GRIN2A):c.3879T>C (p.Asp1293=) rs1199650629 0.00001
NM_001134407.3(GRIN2A):c.1185C>G (p.Ser395=)
NM_001134407.3(GRIN2A):c.1498-4C>T
NM_001134407.3(GRIN2A):c.2391T>C (p.Thr797=)
NM_001134407.3(GRIN2A):c.2494C>T (p.Leu832Phe) rs145495027
NM_001134407.3(GRIN2A):c.2580C>T (p.Leu860=) rs201007843
NM_001134407.3(GRIN2A):c.2694C>T (p.Leu898=) rs569998469
NM_001134407.3(GRIN2A):c.288C>G (p.His96Gln) rs74853460
NM_001134407.3(GRIN2A):c.2985G>C (p.Thr995=) rs781646325
NM_001134407.3(GRIN2A):c.3166A>G (p.Met1056Val)
NM_001134407.3(GRIN2A):c.3246C>T (p.Thr1082=) rs143039009
NM_001134407.3(GRIN2A):c.324C>T (p.Ala108=) rs762110435
NM_001134407.3(GRIN2A):c.3493C>T (p.Leu1165=)
NM_001134407.3(GRIN2A):c.3591T>A (p.Gly1197=) rs532278751
NM_001134407.3(GRIN2A):c.3786C>T (p.Thr1262=)
NM_001134407.3(GRIN2A):c.3915C>G (p.Ser1305Arg) rs199830697
NM_001134407.3(GRIN2A):c.4108T>C (p.Ser1370Pro)
NM_001134407.3(GRIN2A):c.420G>A (p.Pro140=) rs367543126
NM_001134407.3(GRIN2A):c.420G>T (p.Pro140=)
NM_001134407.3(GRIN2A):c.422C>A (p.Thr141Lys) rs78631453
NM_001134407.3(GRIN2A):c.522C>A (p.Thr174=) rs771962690
NM_001134407.3(GRIN2A):c.750G>C (p.Gly250=)
NM_001134407.3(GRIN2A):c.75G>T (p.Ala25=) rs1567354736
NM_001134407.3(GRIN2A):c.90T>C (p.Gly30=) rs1204355370

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