ClinVar Miner

List of variants in gene GRIN2A reported by Genetic Services Laboratory, University of Chicago

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Gene type:
ClinVar version:
Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_001134407.3(GRIN2A):c.2085G>C (p.Arg695=) rs9806806 0.33435
NM_001134407.3(GRIN2A):c.1275G>A (p.Leu425=) rs2229193 0.27838
NM_001134407.3(GRIN2A):c.1329-8C>T rs7193290 0.01998
NM_001134407.3(GRIN2A):c.2190C>T (p.Tyr730=) rs61753382 0.00763
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.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.2277C>T (p.Thr759=) rs148846694 0.00024
NM_001134407.3(GRIN2A):c.3702C>T (p.Phe1234=) rs372083517 0.00022
NM_001134407.3(GRIN2A):c.2636A>G (p.Lys879Arg) rs183029507 0.00007
NM_001134407.3(GRIN2A):c.3103G>A (p.Asp1035Asn) rs540445580 0.00006
NM_001134407.3(GRIN2A):c.623C>T (p.Thr208Ile) rs367543124 0.00006
NM_001134407.3(GRIN2A):c.2664G>A (p.Thr888=) rs113847665 0.00004
NM_001134407.3(GRIN2A):c.547T>A (p.Phe183Ile) rs587780353 0.00004
NM_001134407.3(GRIN2A):c.883G>A (p.Gly295Ser) rs568484876 0.00004
NM_001134407.3(GRIN2A):c.3578T>G (p.Leu1193Trp) rs75761674 0.00003
NM_001134407.3(GRIN2A):c.3624G>A (p.Arg1208=) rs587780350 0.00003
NM_001134407.3(GRIN2A):c.2543G>A (p.Cys848Tyr) rs779911797 0.00002
NM_001134407.3(GRIN2A):c.3037C>T (p.Leu1013=) rs775262289 0.00002
NM_001134407.3(GRIN2A):c.171C>T (p.Pro57=) rs781693549 0.00001
NM_001134407.3(GRIN2A):c.2247C>T (p.Thr749=) rs202026070 0.00001
NM_001134407.3(GRIN2A):c.3619T>C (p.Tyr1207His) rs587780355 0.00001
NM_001134407.3(GRIN2A):c.3636G>A (p.Thr1212=) rs765614514 0.00001
NM_001134407.3(GRIN2A):c.402C>T (p.Ile134=) rs587780352 0.00001
NM_001134407.3(GRIN2A):c.495T>C (p.Tyr165=) rs569491666 0.00001
NM_001134407.3(GRIN2A):c.1329-7dup rs1455515948
NM_001134407.3(GRIN2A):c.1374G>A (p.Gly458=) rs368221866
NM_001134407.3(GRIN2A):c.1667C>T (p.Ser556Phe) rs587780349
NM_001134407.3(GRIN2A):c.19dup (p.Trp7fs) rs2142391531
NM_001134407.3(GRIN2A):c.3064C>A (p.Arg1022Ser) rs560057284
NM_001134407.3(GRIN2A):c.3246C>G (p.Thr1082=) rs143039009
NM_001134407.3(GRIN2A):c.3468A>T (p.Glu1156Asp) rs778180100
NM_001134407.3(GRIN2A):c.3544G>T (p.Asp1182Tyr) rs375160358
NM_001134407.3(GRIN2A):c.3553A>G (p.Lys1185Glu) rs587780354
NM_001134407.3(GRIN2A):c.3701del (p.Phe1234fs) rs886041308
NM_001134407.3(GRIN2A):c.3785C>T (p.Thr1262Ile) rs587780351
NM_001134407.3(GRIN2A):c.4081C>G (p.His1361Asp) rs797045606
NM_001134407.3(GRIN2A):c.415G>T (p.Asp139Tyr) rs1555455852
NM_001134407.3(GRIN2A):c.420G>A (p.Pro140=) rs367543126
NM_001134407.3(GRIN2A):c.422C>T (p.Thr141Met) rs78631453

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