ClinVar Miner

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

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Total variants: 23
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HGVS dbSNP
NM_000833.5(GRIN2A):c.1374G>A (p.Gly458=) rs368221866
NM_000833.5(GRIN2A):c.1517T>C (p.Val506Ala) rs796052543
NM_000833.5(GRIN2A):c.1675G>A (p.Val559Met) rs1476673300
NM_000833.5(GRIN2A):c.3037C>T (p.Leu1013=) rs775262289
NM_000833.5(GRIN2A):c.3163G>C (p.Glu1055Gln) rs370107080
NM_000833.5(GRIN2A):c.3178G>A (p.Asp1060Asn) rs879255358
NM_000833.5(GRIN2A):c.3544G>T (p.Asp1182Tyr) rs375160358
NM_000833.5(GRIN2A):c.3898A>G (p.Arg1300Gly) rs372353067
NM_000833.5(GRIN2A):c.4081C>G (p.His1361Asp) rs797045606
NM_000833.5(GRIN2A):c.415G>T (p.Asp139Tyr) rs1555455852
NM_000833.5(GRIN2A):c.495T>C (p.Tyr165=) rs569491666
NM_001134407.3(GRIN2A):c.171C>T (p.Pro57=) rs781693549
NM_001134407.3(GRIN2A):c.2543G>A (p.Cys848Tyr) rs779911797
NM_001134407.3(GRIN2A):c.2636A>G (p.Lys879Arg) rs183029507
NM_001134407.3(GRIN2A):c.2664G>A (p.Thr888=) rs113847665
NM_001134407.3(GRIN2A):c.2695C>T (p.Arg899Trp) rs796052553
NM_001134407.3(GRIN2A):c.2909G>A (p.Arg970Gln) rs148669437
NM_001134407.3(GRIN2A):c.3064C>A (p.Arg1022Ser) rs560057284
NM_001134407.3(GRIN2A):c.3578T>G (p.Leu1193Trp) rs75761674
NM_001134407.3(GRIN2A):c.3827C>G (p.Ala1276Gly) rs145063086
NM_001134407.3(GRIN2A):c.4307A>G (p.Asn1436Ser) rs77029288
NM_001134407.3(GRIN2A):c.4330G>A (p.Val1444Ile) rs150574045
NM_001134407.3(GRIN2A):c.623C>T (p.Thr208Ile) rs367543124

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