ClinVar Miner

List of variants in gene GRIN2D reported as uncertain significance for Inborn genetic diseases

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Gene type:
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Total variants: 46
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HGVS dbSNP gnomAD frequency
NM_000836.4(GRIN2D):c.3628C>T (p.Pro1210Ser) rs773824115 0.00033
NM_000836.4(GRIN2D):c.3697C>G (p.Pro1233Ala) rs891894351 0.00028
NM_000836.4(GRIN2D):c.3277C>G (p.Pro1093Ala) rs752857170 0.00025
NM_000836.4(GRIN2D):c.3739G>A (p.Ala1247Thr) rs1034596120 0.00020
NM_000836.4(GRIN2D):c.3752A>C (p.His1251Pro) rs896032166 0.00013
NM_000836.4(GRIN2D):c.2806G>A (p.Glu936Lys) rs1271025077 0.00009
NM_000836.4(GRIN2D):c.3673C>T (p.Arg1225Cys) rs1330487131 0.00007
NM_000836.4(GRIN2D):c.2957G>A (p.Gly986Asp) rs926369259 0.00006
NM_000836.4(GRIN2D):c.3888G>C (p.Arg1296Ser) rs375048004 0.00006
NM_000836.4(GRIN2D):c.2827T>G (p.Trp943Gly) rs1388648971 0.00001
NM_000836.4(GRIN2D):c.2860G>A (p.Gly954Ser) rs1282268596 0.00001
NM_000836.4(GRIN2D):c.3124G>C (p.Gly1042Arg) rs1297532606 0.00001
NM_000836.4(GRIN2D):c.3710G>A (p.Arg1237Gln) rs1473583586 0.00001
NM_000836.4(GRIN2D):c.871C>A (p.Pro291Thr) rs753527945 0.00001
NM_000836.4(GRIN2D):c.1007G>A (p.Arg336His)
NM_000836.4(GRIN2D):c.1282G>A (p.Asp428Asn)
NM_000836.4(GRIN2D):c.1421C>T (p.Pro474Leu)
NM_000836.4(GRIN2D):c.2023G>A (p.Ala675Thr) rs1970995171
NM_000836.4(GRIN2D):c.2041A>C (p.Met681Leu) rs1555893359
NM_000836.4(GRIN2D):c.2086C>T (p.Arg696Cys)
NM_000836.4(GRIN2D):c.209G>C (p.Gly70Ala)
NM_000836.4(GRIN2D):c.2117C>T (p.Pro706Leu)
NM_000836.4(GRIN2D):c.223G>T (p.Ala75Ser)
NM_000836.4(GRIN2D):c.224C>T (p.Ala75Val)
NM_000836.4(GRIN2D):c.2393G>C (p.Arg798Pro)
NM_000836.4(GRIN2D):c.2442T>G (p.Asp814Glu)
NM_000836.4(GRIN2D):c.2722C>A (p.Pro908Thr)
NM_000836.4(GRIN2D):c.2752C>G (p.Pro918Ala)
NM_000836.4(GRIN2D):c.2788G>A (p.Ala930Thr)
NM_000836.4(GRIN2D):c.2851C>T (p.Pro951Ser)
NM_000836.4(GRIN2D):c.2857G>C (p.Gly953Arg) rs1439587535
NM_000836.4(GRIN2D):c.2858G>C (p.Gly953Ala)
NM_000836.4(GRIN2D):c.2926G>T (p.Gly976Cys)
NM_000836.4(GRIN2D):c.307C>G (p.Leu103Val)
NM_000836.4(GRIN2D):c.3122T>G (p.Val1041Gly)
NM_000836.4(GRIN2D):c.3157G>A (p.Glu1053Lys)
NM_000836.4(GRIN2D):c.3238G>C (p.Gly1080Arg)
NM_000836.4(GRIN2D):c.3335C>T (p.Pro1112Leu)
NM_000836.4(GRIN2D):c.3583C>G (p.Leu1195Val)
NM_000836.4(GRIN2D):c.3706C>G (p.Pro1236Ala)
NM_000836.4(GRIN2D):c.3724A>C (p.Thr1242Pro)
NM_000836.4(GRIN2D):c.3772G>A (p.Gly1258Arg)
NM_000836.4(GRIN2D):c.3775G>A (p.Gly1259Ser)
NM_000836.4(GRIN2D):c.3865G>C (p.Gly1289Arg)
NM_000836.4(GRIN2D):c.3883C>T (p.Arg1295Cys)
NM_000836.4(GRIN2D):c.997G>A (p.Ala333Thr)

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