ClinVar Miner

List of variants in gene GRIN2A reported as likely benign by Invitae

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Gene type:
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Total variants: 52
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HGVS dbSNP
NM_001134407.3(GRIN2A):c.1008-9C>G rs111844068
NM_001134407.3(GRIN2A):c.1224C>T (p.Ile408=) rs776264780
NM_001134407.3(GRIN2A):c.1354G>A (p.Val452Met) rs145956175
NM_001134407.3(GRIN2A):c.1380C>T (p.Cys460=) rs375291296
NM_001134407.3(GRIN2A):c.1458C>A (p.Gly486=) rs144572467
NM_001134407.3(GRIN2A):c.2007+10C>T rs368110989
NM_001134407.3(GRIN2A):c.2325C>T (p.Ile775=) rs748291723
NM_001134407.3(GRIN2A):c.2505C>T (p.Phe835=) rs771342023
NM_001134407.3(GRIN2A):c.258G>A (p.Val86=) rs774606054
NM_001134407.3(GRIN2A):c.2627T>C (p.Ile876Thr) rs199784503
NM_001134407.3(GRIN2A):c.2760A>G (p.Arg920=) rs80138441
NM_001134407.3(GRIN2A):c.2805T>G (p.Val935=) rs762984731
NM_001134407.3(GRIN2A):c.2852G>T (p.Gly951Val) rs139795367
NM_001134407.3(GRIN2A):c.2877C>T (p.Asn959=) rs756576680
NM_001134407.3(GRIN2A):c.2883C>T (p.Asn961=) rs77705198
NM_001134407.3(GRIN2A):c.288C>T (p.His96=) rs74853460
NM_001134407.3(GRIN2A):c.2985G>C (p.Thr995=) rs781646325
NM_001134407.3(GRIN2A):c.3003C>T (p.Ser1001=) rs199551487
NM_001134407.3(GRIN2A):c.3039G>A (p.Leu1013=) rs577077724
NM_001134407.3(GRIN2A):c.306C>T (p.Asp102=) rs200850130
NM_001134407.3(GRIN2A):c.3108G>A (p.Glu1036=) rs1555482675
NM_001134407.3(GRIN2A):c.3190A>G (p.Thr1064Ala) rs138809301
NM_001134407.3(GRIN2A):c.3211C>T (p.His1071Tyr) rs1555482611
NM_001134407.3(GRIN2A):c.324C>T (p.Ala108=) rs762110435
NM_001134407.3(GRIN2A):c.3366T>G (p.Gly1122=) rs1060504864
NM_001134407.3(GRIN2A):c.3468A>T (p.Glu1156Asp) rs778180100
NM_001134407.3(GRIN2A):c.3630C>T (p.Asn1210=) rs750892541
NM_001134407.3(GRIN2A):c.3687C>A (p.Thr1229=) rs1060504863
NM_001134407.3(GRIN2A):c.3827C>G (p.Ala1276Gly) rs145063086
NM_001134407.3(GRIN2A):c.3953G>A (p.Arg1318Gln) rs149745535
NM_001134407.3(GRIN2A):c.402C>T (p.Ile134=) rs587780352
NM_001134407.3(GRIN2A):c.4140G>C (p.Gly1380=) rs373901698
NM_001134407.3(GRIN2A):c.4176A>G (p.Pro1392=) rs886043681
NM_001134407.3(GRIN2A):c.422C>T (p.Thr141Met) rs78631453
NM_001134407.3(GRIN2A):c.4230G>A (p.Ser1410=) rs762437402
NM_001134407.3(GRIN2A):c.4307A>G (p.Asn1436Ser) rs77029288
NM_001134407.3(GRIN2A):c.4356C>G (p.Arg1452=) rs140093291
NM_001134407.3(GRIN2A):c.468G>A (p.Thr156=) rs773513210
NM_001134407.3(GRIN2A):c.522C>A (p.Thr174=) rs771962690
NM_001134407.3(GRIN2A):c.540C>T (p.Tyr180=) rs745815376
NM_001134407.3(GRIN2A):c.60T>C (p.Gly20=) rs367543130
NM_001134407.3(GRIN2A):c.63G>C (p.Pro21=) rs1060504865
NM_001134407.3(GRIN2A):c.666C>T (p.Ile222=) rs143594020
NM_001134407.3(GRIN2A):c.702C>T (p.Asp234=) rs150208429
NM_001134407.3(GRIN2A):c.741C>T (p.Gly247=) rs141912603
NM_001134407.3(GRIN2A):c.819A>G (p.Pro273=) rs148085725
NM_001134407.3(GRIN2A):c.828C>G (p.Leu276=) rs752295285
NM_001134407.3(GRIN2A):c.837C>G (p.Val279=) rs55885632
NM_001134407.3(GRIN2A):c.882C>T (p.Asp294=) rs201002710
NM_001134407.3(GRIN2A):c.939C>T (p.Ile313=) rs146867324
NM_001134407.3(GRIN2A):c.942C>T (p.Pro314=) rs145172949
NM_001134407.3(GRIN2A):c.963C>T (p.Tyr321=) rs368200727

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