ClinVar Miner

List of variants in gene GRIN2A reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 56
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HGVS dbSNP gnomAD frequency
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.-34C>A rs564039694 0.00134
NM_001134407.3(GRIN2A):c.903C>T (p.Thr301=) rs78241448 0.00119
NM_001134407.3(GRIN2A):c.1354G>A (p.Val452Met) rs145956175 0.00105
NM_001134407.3(GRIN2A):c.4307A>G (p.Asn1436Ser) rs77029288 0.00068
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.2852G>T (p.Gly951Val) rs139795367 0.00042
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.2277C>T (p.Thr759=) rs148846694 0.00024
NM_001134407.3(GRIN2A):c.*8398G>A rs886052517 0.00019
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.*1998A>T rs886052542 0.00010
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.3276C>G (p.Ser1092=) rs775325646 0.00007
NM_001134407.3(GRIN2A):c.2760A>G (p.Arg920=) rs80138441 0.00006
NM_001134407.3(GRIN2A):c.2664G>A (p.Thr888=) rs113847665 0.00004
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.1380C>T (p.Cys460=) rs375291296 0.00002
NM_001134407.3(GRIN2A):c.1652-4G>A rs755304312 0.00002
NM_001134407.3(GRIN2A):c.3192G>A (p.Thr1064=) rs748790515 0.00002
NM_001134407.3(GRIN2A):c.145C>A (p.Arg49Ser) rs1413736970 0.00001
NM_001134407.3(GRIN2A):c.4015A>G (p.Lys1339Glu) rs754686222 0.00001
NM_001134407.3(GRIN2A):c.4209G>A (p.Ser1403=) rs558095250 0.00001
NM_001134407.3(GRIN2A):c.687C>T (p.Leu229=) rs372649219 0.00001
NM_001134407.3(GRIN2A):c.702C>T (p.Asp234=) rs150208429 0.00001
NM_001134407.3(GRIN2A):c.990G>A (p.Pro330=) rs149902963 0.00001
NM_001134407.3(GRIN2A):c.*3166C>T rs886052537
NM_001134407.3(GRIN2A):c.*8362del
NM_001134407.3(GRIN2A):c.1203G>T (p.Pro401=)
NM_001134407.3(GRIN2A):c.1296C>T (p.Asn432=)
NM_001134407.3(GRIN2A):c.1347G>A (p.Gly449=)
NM_001134407.3(GRIN2A):c.1404C>T (p.Ser468=) rs1064797208
NM_001134407.3(GRIN2A):c.2166G>A (p.Thr722=)
NM_001134407.3(GRIN2A):c.2253G>C (p.Gly751=)
NM_001134407.3(GRIN2A):c.225C>T (p.Asn75=) rs527686036
NM_001134407.3(GRIN2A):c.2406C>T (p.Asn802=) rs748977420
NM_001134407.3(GRIN2A):c.2997C>T (p.Ala999=) rs144706004
NM_001134407.3(GRIN2A):c.3153T>C (p.Tyr1051=)
NM_001134407.3(GRIN2A):c.3207G>A (p.Thr1069=) rs752560113
NM_001134407.3(GRIN2A):c.3246C>T (p.Thr1082=) rs143039009
NM_001134407.3(GRIN2A):c.3322A>T (p.Thr1108Ser)
NM_001134407.3(GRIN2A):c.3447C>T (p.Asp1149=) rs2141132170
NM_001134407.3(GRIN2A):c.3468A>T (p.Glu1156Asp) rs778180100
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.422C>T (p.Thr141Met) rs78631453
NM_001134407.3(GRIN2A):c.771C>T (p.Val257=)
NM_001134407.3(GRIN2A):c.795G>A (p.Thr265=)

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