ClinVar Miner

List of variants in gene GRIN2A reported as uncertain significance for not specified

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Total variants: 35
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HGVS dbSNP gnomAD frequency
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.736C>A (p.Leu246Ile) rs555768104 0.00021
NM_001134407.3(GRIN2A):c.2636A>G (p.Lys879Arg) rs183029507 0.00007
NM_001134407.3(GRIN2A):c.3898A>G (p.Arg1300Gly) rs372353067 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.883G>A (p.Gly295Ser) rs568484876 0.00004
NM_001134407.3(GRIN2A):c.989C>T (p.Pro330Leu) rs367543120 0.00004
NM_001134407.3(GRIN2A):c.3578T>G (p.Leu1193Trp) rs75761674 0.00003
NM_001134407.3(GRIN2A):c.2543G>A (p.Cys848Tyr) rs779911797 0.00002
NM_001134407.3(GRIN2A):c.2695C>T (p.Arg899Trp) rs796052553 0.00002
NM_001134407.3(GRIN2A):c.2908C>T (p.Arg970Trp) rs765257420 0.00002
NM_001134407.3(GRIN2A):c.3037C>T (p.Leu1013=) rs775262289 0.00002
NM_001134407.3(GRIN2A):c.1517T>C (p.Val506Ala) rs796052543 0.00001
NM_001134407.3(GRIN2A):c.1675G>A (p.Val559Met) rs1476673300 0.00001
NM_001134407.3(GRIN2A):c.171C>T (p.Pro57=) rs781693549 0.00001
NM_001134407.3(GRIN2A):c.3163G>C (p.Glu1055Gln) rs370107080 0.00001
NM_001134407.3(GRIN2A):c.3722G>A (p.Arg1241Gln) rs886042648 0.00001
NM_001134407.3(GRIN2A):c.3809A>T (p.Asp1270Val) rs750649530 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.1A>T (p.Met1Leu)
NM_001134407.3(GRIN2A):c.3032G>T (p.Arg1011Leu) rs1163766811
NM_001134407.3(GRIN2A):c.3064C>A (p.Arg1022Ser) rs560057284
NM_001134407.3(GRIN2A):c.3178G>A (p.Asp1060Asn) rs879255358
NM_001134407.3(GRIN2A):c.3391G>T (p.Asp1131Tyr) rs1243412120
NM_001134407.3(GRIN2A):c.3544G>T (p.Asp1182Tyr) rs375160358
NM_001134407.3(GRIN2A):c.3712G>A (p.Ala1238Thr) rs2141129928
NM_001134407.3(GRIN2A):c.3914G>C (p.Ser1305Thr)
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.4235G>C (p.Cys1412Ser) rs1900675462

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