ClinVar Miner

List of variants in gene GRIN2A reported as uncertain significance by GeneDx

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Total variants: 57
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HGVS dbSNP
NM_000833.5(GRIN2A):c.1006C>T (p.Pro336Ser) rs148511104
NM_000833.5(GRIN2A):c.1123G>A (p.Val375Met) rs746834456
NM_000833.5(GRIN2A):c.1517T>C (p.Val506Ala) rs796052543
NM_000833.5(GRIN2A):c.172G>A (p.Glu58Lys) rs143833346
NM_000833.5(GRIN2A):c.1943A>G (p.Asn648Ser) rs796052545
NM_000833.5(GRIN2A):c.2103G>C (p.Met701Ile) rs1555491645
NM_000833.5(GRIN2A):c.217C>A (p.Leu73Met) rs775422876
NM_000833.5(GRIN2A):c.2191G>C (p.Asp731His) rs796052549
NM_000833.5(GRIN2A):c.2288T>C (p.Ile763Thr) rs1085307688
NM_000833.5(GRIN2A):c.2356+11G>A rs772691866
NM_000833.5(GRIN2A):c.2696G>A (p.Arg899Gln) rs759145938
NM_000833.5(GRIN2A):c.2796G>C (p.Met932Ile) rs765941753
NM_000833.5(GRIN2A):c.2801T>C (p.Met934Thr) rs540019898
NM_000833.5(GRIN2A):c.2831C>T (p.Ser944Leu) rs1064797025
NM_000833.5(GRIN2A):c.290G>A (p.Gly97Asp) rs1085307680
NM_000833.5(GRIN2A):c.3084G>T (p.Gln1028His) rs796052554
NM_000833.5(GRIN2A):c.3120G>C (p.Glu1040Asp) rs756663920
NM_000833.5(GRIN2A):c.3163G>C (p.Glu1055Gln) rs370107080
NM_000833.5(GRIN2A):c.3266C>T (p.Ser1089Leu) rs1064796981
NM_000833.5(GRIN2A):c.3307C>T (p.Arg1103Cys) rs748879665
NM_000833.5(GRIN2A):c.3332G>T (p.Ser1111Ile) rs796052555
NM_000833.5(GRIN2A):c.3344A>T (p.Asp1115Val) rs796052557
NM_000833.5(GRIN2A):c.3365G>A (p.Gly1122Asp) rs760885908
NM_000833.5(GRIN2A):c.3375G>C (p.Glu1125Asp) rs1177482891
NM_000833.5(GRIN2A):c.3456G>C (p.Gln1152His) rs1085307669
NM_000833.5(GRIN2A):c.3571T>G (p.Phe1191Val) rs562833714
NM_000833.5(GRIN2A):c.3612C>A (p.Ser1204Arg) rs796052558
NM_000833.5(GRIN2A):c.3685A>T (p.Thr1229Ser) rs747136651
NM_000833.5(GRIN2A):c.3745G>A (p.Asp1249Asn) rs754286517
NM_000833.5(GRIN2A):c.3795G>T (p.Gln1265His) rs147556384
NM_000833.5(GRIN2A):c.3796G>A (p.Val1266Ile) rs758615952
NM_000833.5(GRIN2A):c.3884T>C (p.Ile1295Thr) rs757351084
NM_000833.5(GRIN2A):c.4065G>C (p.Lys1355Asn) rs796052559
NM_000833.5(GRIN2A):c.4096C>T (p.Pro1366Ser) rs766598240
NM_000833.5(GRIN2A):c.4305G>C (p.Lys1435Asn) rs1555481948
NM_000833.5(GRIN2A):c.476T>C (p.Leu159Pro) rs1555455805
NM_000833.5(GRIN2A):c.859A>G (p.Ser287Gly) rs1555455615
NM_000833.5(GRIN2A):c.998C>A (p.Thr333Asn) rs370306281
NM_001134407.3(GRIN2A):c.136G>A (p.Val46Met) rs796052542
NM_001134407.3(GRIN2A):c.2165C>T (p.Thr722Met) rs376029542
NM_001134407.3(GRIN2A):c.2563G>A (p.Asp855Asn) rs796052564
NM_001134407.3(GRIN2A):c.2695C>T (p.Arg899Trp) rs796052553
NM_001134407.3(GRIN2A):c.2765C>T (p.Ala922Val) rs200037904
NM_001134407.3(GRIN2A):c.2907C>G (p.Asn969Lys) rs772589363
NM_001134407.3(GRIN2A):c.2909G>A (p.Arg970Gln) rs148669437
NM_001134407.3(GRIN2A):c.3031C>T (p.Arg1011Trp) rs760522909
NM_001134407.3(GRIN2A):c.3064C>T (p.Arg1022Cys) rs560057284
NM_001134407.3(GRIN2A):c.3191C>T (p.Thr1064Met) rs756930722
NM_001134407.3(GRIN2A):c.3308G>A (p.Arg1103His) rs1064796904
NM_001134407.3(GRIN2A):c.3476G>A (p.Arg1159His) rs534440095
NM_001134407.3(GRIN2A):c.3578T>G (p.Leu1193Trp) rs75761674
NM_001134407.3(GRIN2A):c.3659A>C (p.Asn1220Thr) rs1131691913
NM_001134407.3(GRIN2A):c.3961G>C (p.Glu1321Gln) rs370754278
NM_001134407.3(GRIN2A):c.419C>T (p.Pro140Leu) rs142566406
NM_001134407.3(GRIN2A):c.4330G>A (p.Val1444Ile) rs150574045
NM_001134407.3(GRIN2A):c.82_84del (p.Glu28del) rs767188122
NM_001134407.3(GRIN2A):c.869C>T (p.Ala290Val) rs199528312

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