Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.9763108_9769129delCA915949116GRIN2Ac.2357-40_*41del
c.1886-40_*247del
n.1950-40_3686del
c.1886-40_*41del
c.2357-4181_*1806del
c.1946-40_4025del
n.1996-40_3732del
c.1946-40_*247del
c.2357-40_*247del
c.2198-40_*41del
c.2099-40_*41del
c.2513-40_*41del
c.2513-40_*247del
 ClinVar
16g.9764108C>ACA394707870GRIN2Ac.3436G>T (p.Asp1146Tyr)
c.2965G>T (p.Asp989Tyr)
n.3029G>T
c.*806G>T (n.*806G>T)
c.3025G>T (p.Asp1009Tyr)
n.3075G>T
c.3277G>T (p.Asp1093Tyr)
c.3178G>T (p.Asp1060Tyr)
c.3592G>T (p.Asp1198Tyr)
 dbSNP
16g.9764108C>GCA394707871GRIN2Ac.3436G>C (p.Asp1146His)
c.2965G>C (p.Asp989His)
n.3029G>C
c.*806G>C (n.*806G>C)
c.3025G>C (p.Asp1009His)
n.3075G>C
c.3277G>C (p.Asp1093His)
c.3178G>C (p.Asp1060His)
c.3592G>C (p.Asp1198His)
 dbSNP
16g.9764108C>TCA394707872GRIN2Ac.3436G>A (p.Asp1146Asn)
c.2965G>A (p.Asp989Asn)
n.3029G>A
c.*806G>A (n.*806G>A)
c.3025G>A (p.Asp1009Asn)
n.3075G>A
c.3277G>A (p.Asp1093Asn)
c.3178G>A (p.Asp1060Asn)
c.3592G>A (p.Asp1198Asn)
 dbSNP
16g.9764109C>ACA493692854GRIN2Ac.3435G>T (p.Val1145=)
c.2964G>T (p.Val988=)
n.3028G>T
c.*805G>T (n.*805G>T)
c.3024G>T (p.Val1008=)
n.3074G>T
c.3276G>T (p.Val1092=)
c.3177G>T (p.Val1059=)
c.3591G>T (p.Val1197=)
 dbSNP
16g.9764109C>GCA493692855GRIN2Ac.3435G>C (p.Val1145=)
c.2964G>C (p.Val988=)
n.3028G>C
c.*805G>C (n.*805G>C)
c.3024G>C (p.Val1008=)
n.3074G>C
c.3276G>C (p.Val1092=)
c.3177G>C (p.Val1059=)
c.3591G>C (p.Val1197=)
16g.9764109C>TCA493692856GRIN2Ac.3435G>A (p.Val1145=)
c.2964G>A (p.Val988=)
n.3028G>A
c.*805G>A (n.*805G>A)
c.3024G>A (p.Val1008=)
n.3074G>A
c.3276G>A (p.Val1092=)
c.3177G>A (p.Val1059=)
c.3591G>A (p.Val1197=)
 dbSNP
16g.9764110A>CCA394707875GRIN2Ac.3434T>G (p.Val1145Gly)
c.2963T>G (p.Val988Gly)
n.3027T>G
c.*804T>G (n.*804T>G)
c.3023T>G (p.Val1008Gly)
n.3073T>G
c.3275T>G (p.Val1092Gly)
c.3176T>G (p.Val1059Gly)
c.3590T>G (p.Val1197Gly)
16g.9764110A>GCA394707874GRIN2Ac.3434T>C (p.Val1145Ala)
c.2963T>C (p.Val988Ala)
n.3027T>C
c.*804T>C (n.*804T>C)
c.3023T>C (p.Val1008Ala)
n.3073T>C
c.3275T>C (p.Val1092Ala)
c.3176T>C (p.Val1059Ala)
c.3590T>C (p.Val1197Ala)
 dbSNP
16g.9764110A>TCA394707873GRIN2Ac.3434T>A (p.Val1145Glu)
c.2963T>A (p.Val988Glu)
n.3027T>A
c.*804T>A (n.*804T>A)
c.3023T>A (p.Val1008Glu)
n.3073T>A
c.3275T>A (p.Val1092Glu)
c.3176T>A (p.Val1059Glu)
c.3590T>A (p.Val1197Glu)
 dbSNP
16g.9764111C>ACA394707876GRIN2Ac.3433G>T (p.Val1145Leu)
c.2962G>T (p.Val988Leu)
n.3026G>T
c.*803G>T (n.*803G>T)
c.3022G>T (p.Val1008Leu)
n.3072G>T
c.3274G>T (p.Val1092Leu)
c.3175G>T (p.Val1059Leu)
c.3589G>T (p.Val1197Leu)
 dbSNP gnomAD v4
16g.9764111C=CA2206693054GRIN2Ac.3433G= (p.Val1145=)
c.2962G= (p.Val988=)
n.3026G=
c.*803G= (n.*803G=)
c.3022G= (p.Val1008=)
n.3072G=
c.3274G= (p.Val1092=)
c.3175G= (p.Val1059=)
c.3589G= (p.Val1197=)
16g.9764111C>GCA394707877GRIN2Ac.3433G>C (p.Val1145Leu)
c.2962G>C (p.Val988Leu)
n.3026G>C
c.*803G>C (n.*803G>C)
c.3022G>C (p.Val1008Leu)
n.3072G>C
c.3274G>C (p.Val1092Leu)
c.3175G>C (p.Val1059Leu)
c.3589G>C (p.Val1197Leu)
 dbSNP
16g.9764111C>TCA7896316GRIN2Ac.3433G>A (p.Val1145Met)
c.2962G>A (p.Val988Met)
n.3026G>A
c.*803G>A (n.*803G>A)
c.3022G>A (p.Val1008Met)
n.3072G>A
c.3274G>A (p.Val1092Met)
c.3175G>A (p.Val1059Met)
c.3589G>A (p.Val1197Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.9764112G>ACA7896317GRIN2Ac.3432C>T (p.Asn1144=)
c.2961C>T (p.Asn987=)
n.3025C>T
c.*802C>T (n.*802C>T)
c.3021C>T (p.Asn1007=)
n.3071C>T
c.3273C>T (p.Asn1091=)
c.3174C>T (p.Asn1058=)
c.3588C>T (p.Asn1196=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.9764112G>CCA394707878GRIN2Ac.3432C>G (p.Asn1144Lys)
c.2961C>G (p.Asn987Lys)
n.3025C>G
c.*802C>G (n.*802C>G)
c.3021C>G (p.Asn1007Lys)
n.3071C>G
c.3273C>G (p.Asn1091Lys)
c.3174C>G (p.Asn1058Lys)
c.3588C>G (p.Asn1196Lys)
 dbSNP
16g.9764112G=CA2206693055GRIN2Ac.3432C= (p.Asn1144=)
c.2961C= (p.Asn987=)
n.3025C=
c.*802C= (n.*802C=)
c.3021C= (p.Asn1007=)
n.3071C=
c.3273C= (p.Asn1091=)
c.3174C= (p.Asn1058=)
c.3588C= (p.Asn1196=)
16g.9764112G>TCA394707879GRIN2Ac.3432C>A (p.Asn1144Lys)
c.2961C>A (p.Asn987Lys)
n.3025C>A
c.*802C>A (n.*802C>A)
c.3021C>A (p.Asn1007Lys)
n.3071C>A
c.3273C>A (p.Asn1091Lys)
c.3174C>A (p.Asn1058Lys)
c.3588C>A (p.Asn1196Lys)
 ClinVar dbSNP gnomAD v2 gnomAD v4
16g.9764113T>ACA394707880GRIN2Ac.3431A>T (p.Asn1144Ile)
c.2960A>T (p.Asn987Ile)
n.3024A>T
c.*801A>T (n.*801A>T)
c.3020A>T (p.Asn1007Ile)
n.3070A>T
c.3272A>T (p.Asn1091Ile)
c.3173A>T (p.Asn1058Ile)
c.3587A>T (p.Asn1196Ile)
 dbSNP
16g.9764113T>CCA394707882GRIN2Ac.3431A>G (p.Asn1144Ser)
c.2960A>G (p.Asn987Ser)
n.3024A>G
c.*801A>G (n.*801A>G)
c.3020A>G (p.Asn1007Ser)
n.3070A>G
c.3272A>G (p.Asn1091Ser)
c.3173A>G (p.Asn1058Ser)
c.3587A>G (p.Asn1196Ser)
 dbSNP
16g.9764113T>GCA394707881GRIN2Ac.3431A>C (p.Asn1144Thr)
c.2960A>C (p.Asn987Thr)
n.3024A>C
c.*801A>C (n.*801A>C)
c.3020A>C (p.Asn1007Thr)
n.3070A>C
c.3272A>C (p.Asn1091Thr)
c.3173A>C (p.Asn1058Thr)
c.3587A>C (p.Asn1196Thr)
 dbSNP
16g.9764114T>ACA394707883GRIN2Ac.3430A>T (p.Asn1144Tyr)
c.2959A>T (p.Asn987Tyr)
n.3023A>T
c.*800A>T (n.*800A>T)
c.3019A>T (p.Asn1007Tyr)
n.3069A>T
c.3271A>T (p.Asn1091Tyr)
c.3172A>T (p.Asn1058Tyr)
c.3586A>T (p.Asn1196Tyr)
 dbSNP
16g.9764114T>CCA394707884GRIN2Ac.3430A>G (p.Asn1144Asp)
c.2959A>G (p.Asn987Asp)
n.3023A>G
c.*800A>G (n.*800A>G)
c.3019A>G (p.Asn1007Asp)
n.3069A>G
c.3271A>G (p.Asn1091Asp)
c.3172A>G (p.Asn1058Asp)
c.3586A>G (p.Asn1196Asp)
16g.9764114T>GCA394707885GRIN2Ac.3430A>C (p.Asn1144His)
c.2959A>C (p.Asn987His)
n.3023A>C
c.*800A>C (n.*800A>C)
c.3019A>C (p.Asn1007His)
n.3069A>C
c.3271A>C (p.Asn1091His)
c.3172A>C (p.Asn1058His)
c.3586A>C (p.Asn1196His)
 dbSNP
16g.9764115C>ACA394707886GRIN2Ac.3429G>T (p.Glu1143Asp)
c.2958G>T (p.Glu986Asp)
n.3022G>T
c.*799G>T (n.*799G>T)
c.3018G>T (p.Glu1006Asp)
n.3068G>T
c.3270G>T (p.Glu1090Asp)
c.3171G>T (p.Glu1057Asp)
c.3585G>T (p.Glu1195Asp)
16g.9764115C>GCA394707887GRIN2Ac.3429G>C (p.Glu1143Asp)
c.2958G>C (p.Glu986Asp)
n.3022G>C
c.*799G>C (n.*799G>C)
c.3018G>C (p.Glu1006Asp)
n.3068G>C
c.3270G>C (p.Glu1090Asp)
c.3171G>C (p.Glu1057Asp)
c.3585G>C (p.Glu1195Asp)
16g.9764115C>TCA493692865GRIN2Ac.3429G>A (p.Glu1143=)
c.2958G>A (p.Glu986=)
n.3022G>A
c.*799G>A (n.*799G>A)
c.3018G>A (p.Glu1006=)
n.3068G>A
c.3270G>A (p.Glu1090=)
c.3171G>A (p.Glu1057=)
c.3585G>A (p.Glu1195=)
16g.9764116T>ACA394707888GRIN2Ac.3428A>T (p.Glu1143Val)
c.2957A>T (p.Glu986Val)
n.3021A>T
c.*798A>T (n.*798A>T)
c.3017A>T (p.Glu1006Val)
n.3067A>T
c.3269A>T (p.Glu1090Val)
c.3170A>T (p.Glu1057Val)
c.3584A>T (p.Glu1195Val)
16g.9764116T>CCA394707889GRIN2Ac.3428A>G (p.Glu1143Gly)
c.2957A>G (p.Glu986Gly)
n.3021A>G
c.*798A>G (n.*798A>G)
c.3017A>G (p.Glu1006Gly)
n.3067A>G
c.3269A>G (p.Glu1090Gly)
c.3170A>G (p.Glu1057Gly)
c.3584A>G (p.Glu1195Gly)
16g.9764116T>GCA394707890GRIN2Ac.3428A>C (p.Glu1143Ala)
c.2957A>C (p.Glu986Ala)
n.3021A>C
c.*798A>C (n.*798A>C)
c.3017A>C (p.Glu1006Ala)
n.3067A>C
c.3269A>C (p.Glu1090Ala)
c.3170A>C (p.Glu1057Ala)
c.3584A>C (p.Glu1195Ala)
16g.9764117C>ACA394707891GRIN2Ac.3427G>T (p.Glu1143Ter)
c.2956G>T (p.Glu986Ter)
n.3020G>T
c.*797G>T (n.*797G>T)
c.3016G>T (p.Glu1006Ter)
n.3066G>T
c.3268G>T (p.Glu1090Ter)
c.3169G>T (p.Glu1057Ter)
c.3583G>T (p.Glu1195Ter)
 dbSNP
16g.9764117C=CA2206693056GRIN2Ac.3427G= (p.Glu1143=)
c.2956G= (p.Glu986=)
n.3020G=
c.*797G= (n.*797G=)
c.3016G= (p.Glu1006=)
n.3066G=
c.3268G= (p.Glu1090=)
c.3169G= (p.Glu1057=)
c.3583G= (p.Glu1195=)
16g.9764117C>GCA394707892GRIN2Ac.3427G>C (p.Glu1143Gln)
c.2956G>C (p.Glu986Gln)
n.3020G>C
c.*797G>C (n.*797G>C)
c.3016G>C (p.Glu1006Gln)
n.3066G>C
c.3268G>C (p.Glu1090Gln)
c.3169G>C (p.Glu1057Gln)
c.3583G>C (p.Glu1195Gln)
 dbSNP
16g.9764117C>TCA7896318GRIN2Ac.3427G>A (p.Glu1143Lys)
c.2956G>A (p.Glu986Lys)
n.3020G>A
c.*797G>A (n.*797G>A)
c.3016G>A (p.Glu1006Lys)
n.3066G>A
c.3268G>A (p.Glu1090Lys)
c.3169G>A (p.Glu1057Lys)
c.3583G>A (p.Glu1195Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.9764118G>ACA7896319GRIN2Ac.3426C>T (p.Pro1142=)
c.2955C>T (p.Pro985=)
n.3019C>T
c.*796C>T (n.*796C>T)
c.3015C>T (p.Pro1005=)
n.3065C>T
c.3267C>T (p.Pro1089=)
c.3168C>T (p.Pro1056=)
c.3582C>T (p.Pro1194=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.9764118G>CCA493692866GRIN2Ac.3426C>G (p.Pro1142=)
c.2955C>G (p.Pro985=)
n.3019C>G
c.*796C>G (n.*796C>G)
c.3015C>G (p.Pro1005=)
n.3065C>G
c.3267C>G (p.Pro1089=)
c.3168C>G (p.Pro1056=)
c.3582C>G (p.Pro1194=)
 dbSNP
16g.9764118G=CA2206693057GRIN2Ac.3426C= (p.Pro1142=)
c.2955C= (p.Pro985=)
n.3019C=
c.*796C= (n.*796C=)
c.3015C= (p.Pro1005=)
n.3065C=
c.3267C= (p.Pro1089=)
c.3168C= (p.Pro1056=)
c.3582C= (p.Pro1194=)
16g.9764118G>TCA493692867GRIN2Ac.3426C>A (p.Pro1142=)
c.2955C>A (p.Pro985=)
n.3019C>A
c.*796C>A (n.*796C>A)
c.3015C>A (p.Pro1005=)
n.3065C>A
c.3267C>A (p.Pro1089=)
c.3168C>A (p.Pro1056=)
c.3582C>A (p.Pro1194=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.9764120delCA2580092130GRIN2Ac.3426del (p.Glu1143ArgfsTer25)
c.2955del (p.Glu986ArgfsTer25)
n.3019del
c.*796del (n.*796del)
c.3015del (p.Glu1006ArgfsTer25)
n.3065del
c.3267del (p.Glu1090ArgfsTer25)
c.3168del (p.Glu1057ArgfsTer25)
c.3582del (p.Glu1195ArgfsTer25)
 ClinVar
16g.9764119G>ACA394707894GRIN2Ac.3425C>T (p.Pro1142Leu)
c.2954C>T (p.Pro985Leu)
n.3018C>T
c.*795C>T (n.*795C>T)
c.3014C>T (p.Pro1005Leu)
n.3064C>T
c.3266C>T (p.Pro1089Leu)
c.3167C>T (p.Pro1056Leu)
c.3581C>T (p.Pro1194Leu)
 dbSNP
16g.9764119G>CCA394707895GRIN2Ac.3425C>G (p.Pro1142Arg)
c.2954C>G (p.Pro985Arg)
n.3018C>G
c.*795C>G (n.*795C>G)
c.3014C>G (p.Pro1005Arg)
n.3064C>G
c.3266C>G (p.Pro1089Arg)
c.3167C>G (p.Pro1056Arg)
c.3581C>G (p.Pro1194Arg)
 dbSNP
16g.9764119G>TCA394707893GRIN2Ac.3425C>A (p.Pro1142His)
c.2954C>A (p.Pro985His)
n.3018C>A
c.*795C>A (n.*795C>A)
c.3014C>A (p.Pro1005His)
n.3064C>A
c.3266C>A (p.Pro1089His)
c.3167C>A (p.Pro1056His)
c.3581C>A (p.Pro1194His)
 dbSNP
16g.9764120G>ACA394707896GRIN2Ac.3424C>T (p.Pro1142Ser)
c.2953C>T (p.Pro985Ser)
n.3017C>T
c.*794C>T (n.*794C>T)
c.3013C>T (p.Pro1005Ser)
n.3063C>T
c.3265C>T (p.Pro1089Ser)
c.3166C>T (p.Pro1056Ser)
c.3580C>T (p.Pro1194Ser)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.9764120G>CCA394707897GRIN2Ac.3424C>G (p.Pro1142Ala)
c.2953C>G (p.Pro985Ala)
n.3017C>G
c.*794C>G (n.*794C>G)
c.3013C>G (p.Pro1005Ala)
n.3063C>G
c.3265C>G (p.Pro1089Ala)
c.3166C>G (p.Pro1056Ala)
c.3580C>G (p.Pro1194Ala)
 dbSNP
16g.9764120G=CA2206693058GRIN2Ac.3424C= (p.Pro1142=)
c.2953C= (p.Pro985=)
n.3017C=
c.*794C= (n.*794C=)
c.3013C= (p.Pro1005=)
n.3063C=
c.3265C= (p.Pro1089=)
c.3166C= (p.Pro1056=)
c.3580C= (p.Pro1194=)
16g.9764120G>TCA394707898GRIN2Ac.3424C>A (p.Pro1142Thr)
c.2953C>A (p.Pro985Thr)
n.3017C>A
c.*794C>A (n.*794C>A)
c.3013C>A (p.Pro1005Thr)
n.3063C>A
c.3265C>A (p.Pro1089Thr)
c.3166C>A (p.Pro1056Thr)
c.3580C>A (p.Pro1194Thr)
 dbSNP COSMIC
16g.9764121C>ACA7896321GRIN2Ac.3423G>T (p.Leu1141=)
c.2952G>T (p.Leu984=)
n.3016G>T
c.*793G>T (n.*793G>T)
c.3012G>T (p.Leu1004=)
n.3062G>T
c.3264G>T (p.Leu1088=)
c.3165G>T (p.Leu1055=)
c.3579G>T (p.Leu1193=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.9764121C=CA2206693059GRIN2Ac.3423G= (p.Leu1141=)
c.2952G= (p.Leu984=)
n.3016G=
c.*793G= (n.*793G=)
c.3012G= (p.Leu1004=)
n.3062G=
c.3264G= (p.Leu1088=)
c.3165G= (p.Leu1055=)
c.3579G= (p.Leu1193=)
16g.9764121C>GCA7896320GRIN2Ac.3423G>C (p.Leu1141=)
c.2952G>C (p.Leu984=)
n.3016G>C
c.*793G>C (n.*793G>C)
c.3012G>C (p.Leu1004=)
n.3062G>C
c.3264G>C (p.Leu1088=)
c.3165G>C (p.Leu1055=)
c.3579G>C (p.Leu1193=)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.9764121C>TCA493692870GRIN2Ac.3423G>A (p.Leu1141=)
c.2952G>A (p.Leu984=)
n.3016G>A
c.*793G>A (n.*793G>A)
c.3012G>A (p.Leu1004=)
n.3062G>A
c.3264G>A (p.Leu1088=)
c.3165G>A (p.Leu1055=)
c.3579G>A (p.Leu1193=)
16g.9764122A=CA2206693060GRIN2Ac.3422T= (p.Leu1141=)
c.2951T= (p.Leu984=)
n.3015T=
c.*792T= (n.*792T=)
c.3011T= (p.Leu1004=)
n.3061T=
c.3263T= (p.Leu1088=)
c.3164T= (p.Leu1055=)
c.3578T= (p.Leu1193=)
16g.9764122A>CCA394707901GRIN2Ac.3422T>G (p.Leu1141Arg)
c.2951T>G (p.Leu984Arg)
n.3015T>G
c.*792T>G (n.*792T>G)
c.3011T>G (p.Leu1004Arg)
n.3061T>G
c.3263T>G (p.Leu1088Arg)
c.3164T>G (p.Leu1055Arg)
c.3578T>G (p.Leu1193Arg)
16g.9764122A>GCA394707899GRIN2Ac.3422T>C (p.Leu1141Pro)
c.2951T>C (p.Leu984Pro)
n.3015T>C
c.*792T>C (n.*792T>C)
c.3011T>C (p.Leu1004Pro)
n.3061T>C
c.3263T>C (p.Leu1088Pro)
c.3164T>C (p.Leu1055Pro)
c.3578T>C (p.Leu1193Pro)
 dbSNP
16g.9764122A>TCA394707900GRIN2Ac.3422T>A (p.Leu1141Gln)
c.2951T>A (p.Leu984Gln)
n.3015T>A
c.*792T>A (n.*792T>A)
c.3011T>A (p.Leu1004Gln)
n.3061T>A
c.3263T>A (p.Leu1088Gln)
c.3164T>A (p.Leu1055Gln)
c.3578T>A (p.Leu1193Gln)
 dbSNP
16g.9764123G>ACA493692871GRIN2Ac.3421C>T (p.Leu1141=)
c.2950C>T (p.Leu984=)
n.3014C>T
c.*791C>T (n.*791C>T)
c.3010C>T (p.Leu1004=)
n.3060C>T
c.3262C>T (p.Leu1088=)
c.3163C>T (p.Leu1055=)
c.3577C>T (p.Leu1193=)
 dbSNP gnomAD v4
16g.9764123G>CCA394707902GRIN2Ac.3421C>G (p.Leu1141Val)
c.2950C>G (p.Leu984Val)
n.3014C>G
c.*791C>G (n.*791C>G)
c.3010C>G (p.Leu1004Val)
n.3060C>G
c.3262C>G (p.Leu1088Val)
c.3163C>G (p.Leu1055Val)
c.3577C>G (p.Leu1193Val)
 dbSNP
16g.9764123G>TCA394707903GRIN2Ac.3421C>A (p.Leu1141Met)
c.2950C>A (p.Leu984Met)
n.3014C>A
c.*791C>A (n.*791C>A)
c.3010C>A (p.Leu1004Met)
n.3060C>A
c.3262C>A (p.Leu1088Met)
c.3163C>A (p.Leu1055Met)
c.3577C>A (p.Leu1193Met)
16g.9764124G>ACA493692875GRIN2Ac.3420C>T (p.Thr1140=)
c.2949C>T (p.Thr983=)
n.3013C>T
c.*790C>T (n.*790C>T)
c.3009C>T (p.Thr1003=)
n.3059C>T
c.3261C>T (p.Thr1087=)
c.3162C>T (p.Thr1054=)
c.3576C>T (p.Thr1192=)
 dbSNP
16g.9764124G>CCA493692876GRIN2Ac.3420C>G (p.Thr1140=)
c.2949C>G (p.Thr983=)
n.3013C>G
c.*790C>G (n.*790C>G)
c.3009C>G (p.Thr1003=)
n.3059C>G
c.3261C>G (p.Thr1087=)
c.3162C>G (p.Thr1054=)
c.3576C>G (p.Thr1192=)
 dbSNP
16g.9764124G=CA2206693061GRIN2Ac.3420C= (p.Thr1140=)
c.2949C= (p.Thr983=)
n.3013C=
c.*790C= (n.*790C=)
c.3009C= (p.Thr1003=)
n.3059C=
c.3261C= (p.Thr1087=)
c.3162C= (p.Thr1054=)
c.3576C= (p.Thr1192=)
16g.9764124G>TCA493692878GRIN2Ac.3420C>A (p.Thr1140=)
c.2949C>A (p.Thr983=)
n.3013C>A
c.*790C>A (n.*790C>A)
c.3009C>A (p.Thr1003=)
n.3059C>A
c.3261C>A (p.Thr1087=)
c.3162C>A (p.Thr1054=)
c.3576C>A (p.Thr1192=)
 dbSNP
16g.9764125G>ACA7896322GRIN2Ac.3419C>T (p.Thr1140Ile)
c.2948C>T (p.Thr983Ile)
n.3012C>T
c.*789C>T (n.*789C>T)
c.3008C>T (p.Thr1003Ile)
n.3058C>T
c.3260C>T (p.Thr1087Ile)
c.3161C>T (p.Thr1054Ile)
c.3575C>T (p.Thr1192Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.9764125G>CCA394707904GRIN2Ac.3419C>G (p.Thr1140Ser)
c.2948C>G (p.Thr983Ser)
n.3012C>G
c.*789C>G (n.*789C>G)
c.3008C>G (p.Thr1003Ser)
n.3058C>G
c.3260C>G (p.Thr1087Ser)
c.3161C>G (p.Thr1054Ser)
c.3575C>G (p.Thr1192Ser)
 dbSNP
16g.9764125G=CA2206693062GRIN2Ac.3419C= (p.Thr1140=)
c.2948C= (p.Thr983=)
n.3012C=
c.*789C= (n.*789C=)
c.3008C= (p.Thr1003=)
n.3058C=
c.3260C= (p.Thr1087=)
c.3161C= (p.Thr1054=)
c.3575C= (p.Thr1192=)
16g.9764125G>TCA394707905GRIN2Ac.3419C>A (p.Thr1140Asn)
c.2948C>A (p.Thr983Asn)
n.3012C>A
c.*789C>A (n.*789C>A)
c.3008C>A (p.Thr1003Asn)
n.3058C>A
c.3260C>A (p.Thr1087Asn)
c.3161C>A (p.Thr1054Asn)
c.3575C>A (p.Thr1192Asn)
 gnomAD v4
16g.9764126T>ACA394707906GRIN2Ac.3418A>T (p.Thr1140Ser)
c.2947A>T (p.Thr983Ser)
n.3011A>T
c.*788A>T (n.*788A>T)
c.3007A>T (p.Thr1003Ser)
n.3057A>T
c.3259A>T (p.Thr1087Ser)
c.3160A>T (p.Thr1054Ser)
c.3574A>T (p.Thr1192Ser)
 dbSNP gnomAD v4
16g.9764126T>CCA394707908GRIN2Ac.3418A>G (p.Thr1140Ala)
c.2947A>G (p.Thr983Ala)
n.3011A>G
c.*788A>G (n.*788A>G)
c.3007A>G (p.Thr1003Ala)
n.3057A>G
c.3259A>G (p.Thr1087Ala)
c.3160A>G (p.Thr1054Ala)
c.3574A>G (p.Thr1192Ala)
 dbSNP
16g.9764126T>GCA394707907GRIN2Ac.3418A>C (p.Thr1140Pro)
c.2947A>C (p.Thr983Pro)
n.3011A>C
c.*788A>C (n.*788A>C)
c.3007A>C (p.Thr1003Pro)
n.3057A>C
c.3259A>C (p.Thr1087Pro)
c.3160A>C (p.Thr1054Pro)
c.3574A>C (p.Thr1192Pro)
 dbSNP
16g.9764127C>ACA493692882GRIN2Ac.3417G>T (p.Val1139=)
c.2946G>T (p.Val982=)
n.3010G>T
c.*787G>T (n.*787G>T)
c.3006G>T (p.Val1002=)
n.3056G>T
c.3258G>T (p.Val1086=)
c.3159G>T (p.Val1053=)
c.3573G>T (p.Val1191=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
16g.9764127C=CA2206693063GRIN2Ac.3417G= (p.Val1139=)
c.2946G= (p.Val982=)
n.3010G=
c.*787G= (n.*787G=)
c.3006G= (p.Val1002=)
n.3056G=
c.3258G= (p.Val1086=)
c.3159G= (p.Val1053=)
c.3573G= (p.Val1191=)
16g.9764127C>GCA493692884GRIN2Ac.3417G>C (p.Val1139=)
c.2946G>C (p.Val982=)
n.3010G>C
c.*787G>C (n.*787G>C)
c.3006G>C (p.Val1002=)
n.3056G>C
c.3258G>C (p.Val1086=)
c.3159G>C (p.Val1053=)
c.3573G>C (p.Val1191=)
16g.9764127C>TCA493692883GRIN2Ac.3417G>A (p.Val1139=)
c.2946G>A (p.Val982=)
n.3010G>A
c.*787G>A (n.*787G>A)
c.3006G>A (p.Val1002=)
n.3056G>A
c.3258G>A (p.Val1086=)
c.3159G>A (p.Val1053=)
c.3573G>A (p.Val1191=)
 dbSNP gnomAD v4 COSMIC
16g.9764128A=CA2206693064GRIN2Ac.3416T= (p.Val1139=)
c.2945T= (p.Val982=)
n.3009T=
c.*786T= (n.*786T=)
c.3005T= (p.Val1002=)
n.3055T=
c.3257T= (p.Val1086=)
c.3158T= (p.Val1053=)
c.3572T= (p.Val1191=)
16g.9764128A>CCA394707909GRIN2Ac.3416T>G (p.Val1139Gly)
c.2945T>G (p.Val982Gly)
n.3009T>G
c.*786T>G (n.*786T>G)
c.3005T>G (p.Val1002Gly)
n.3055T>G
c.3257T>G (p.Val1086Gly)
c.3158T>G (p.Val1053Gly)
c.3572T>G (p.Val1191Gly)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.9764128A>GCA394707910GRIN2Ac.3416T>C (p.Val1139Ala)
c.2945T>C (p.Val982Ala)
n.3009T>C
c.*786T>C (n.*786T>C)
c.3005T>C (p.Val1002Ala)
n.3055T>C
c.3257T>C (p.Val1086Ala)
c.3158T>C (p.Val1053Ala)
c.3572T>C (p.Val1191Ala)
 dbSNP gnomAD v4
16g.9764128A>TCA394707911GRIN2Ac.3416T>A (p.Val1139Glu)
c.2945T>A (p.Val982Glu)
n.3009T>A
c.*786T>A (n.*786T>A)
c.3005T>A (p.Val1002Glu)
n.3055T>A
c.3257T>A (p.Val1086Glu)
c.3158T>A (p.Val1053Glu)
c.3572T>A (p.Val1191Glu)
 dbSNP
16g.9764129C>ACA394707912GRIN2Ac.3415G>T (p.Val1139Leu)
c.2944G>T (p.Val982Leu)
n.3008G>T
c.*785G>T (n.*785G>T)
c.3004G>T (p.Val1002Leu)
n.3054G>T
c.3256G>T (p.Val1086Leu)
c.3157G>T (p.Val1053Leu)
c.3571G>T (p.Val1191Leu)
 dbSNP
16g.9764129C>GCA394707913GRIN2Ac.3415G>C (p.Val1139Leu)
c.2944G>C (p.Val982Leu)
n.3008G>C
c.*785G>C (n.*785G>C)
c.3004G>C (p.Val1002Leu)
n.3054G>C
c.3256G>C (p.Val1086Leu)
c.3157G>C (p.Val1053Leu)
c.3571G>C (p.Val1191Leu)
 dbSNP
16g.9764129C>TCA394707914GRIN2Ac.3415G>A (p.Val1139Met)
c.2944G>A (p.Val982Met)
n.3008G>A
c.*785G>A (n.*785G>A)
c.3004G>A (p.Val1002Met)
n.3054G>A
c.3256G>A (p.Val1086Met)
c.3157G>A (p.Val1053Met)
c.3571G>A (p.Val1191Met)
 dbSNP gnomAD v4
16g.9764130A=CA2206693065GRIN2Ac.3414T= (p.Asn1138=)
c.2943T= (p.Asn981=)
n.3007T=
c.*784T= (n.*784T=)
c.3003T= (p.Asn1001=)
n.3053T=
c.3255T= (p.Asn1085=)
c.3156T= (p.Asn1052=)
c.3570T= (p.Asn1190=)
16g.9764130A>CCA394707915GRIN2Ac.3414T>G (p.Asn1138Lys)
c.2943T>G (p.Asn981Lys)
n.3007T>G
c.*784T>G (n.*784T>G)
c.3003T>G (p.Asn1001Lys)
n.3053T>G
c.3255T>G (p.Asn1085Lys)
c.3156T>G (p.Asn1052Lys)
c.3570T>G (p.Asn1190Lys)
16g.9764130A>GCA493692889GRIN2Ac.3414T>C (p.Asn1138=)
c.2943T>C (p.Asn981=)
n.3007T>C
c.*784T>C (n.*784T>C)
c.3003T>C (p.Asn1001=)
n.3053T>C
c.3255T>C (p.Asn1085=)
c.3156T>C (p.Asn1052=)
c.3570T>C (p.Asn1190=)
 dbSNP
16g.9764130A>TCA394707916GRIN2Ac.3414T>A (p.Asn1138Lys)
c.2943T>A (p.Asn981Lys)
n.3007T>A
c.*784T>A (n.*784T>A)
c.3003T>A (p.Asn1001Lys)
n.3053T>A
c.3255T>A (p.Asn1085Lys)
c.3156T>A (p.Asn1052Lys)
c.3570T>A (p.Asn1190Lys)
16g.9764131T>ACA225879GRIN2Ac.3413A>T (p.Asn1138Ile)
c.2942A>T (p.Asn981Ile)
n.3006A>T
c.*783A>T (n.*783A>T)
c.3002A>T (p.Asn1001Ile)
n.3052A>T
c.3254A>T (p.Asn1085Ile)
c.3155A>T (p.Asn1052Ile)
c.3569A>T (p.Asn1190Ile)
 ClinVar dbSNP gnomAD v4
16g.9764131T>CCA394707917GRIN2Ac.3413A>G (p.Asn1138Ser)
c.2942A>G (p.Asn981Ser)
n.3006A>G
c.*783A>G (n.*783A>G)
c.3002A>G (p.Asn1001Ser)
n.3052A>G
c.3254A>G (p.Asn1085Ser)
c.3155A>G (p.Asn1052Ser)
c.3569A>G (p.Asn1190Ser)
 ClinVar dbSNP gnomAD v4
16g.9764131T>GCA394707918GRIN2Ac.3413A>C (p.Asn1138Thr)
c.2942A>C (p.Asn981Thr)
n.3006A>C
c.*783A>C (n.*783A>C)
c.3002A>C (p.Asn1001Thr)
n.3052A>C
c.3254A>C (p.Asn1085Thr)
c.3155A>C (p.Asn1052Thr)
c.3569A>C (p.Asn1190Thr)
 dbSNP
16g.9764131T=CA2206693066GRIN2Ac.3413A= (p.Asn1138=)
c.2942A= (p.Asn981=)
n.3006A=
c.*783A= (n.*783A=)
c.3002A= (p.Asn1001=)
n.3052A=
c.3254A= (p.Asn1085=)
c.3155A= (p.Asn1052=)
c.3569A= (p.Asn1190=)
16g.9764132T>ACA394707919GRIN2Ac.3412A>T (p.Asn1138Tyr)
c.2941A>T (p.Asn981Tyr)
n.3005A>T
c.*782A>T (n.*782A>T)
c.3001A>T (p.Asn1001Tyr)
n.3051A>T
c.3253A>T (p.Asn1085Tyr)
c.3154A>T (p.Asn1052Tyr)
c.3568A>T (p.Asn1190Tyr)
16g.9764132T>CCA394707920GRIN2Ac.3412A>G (p.Asn1138Asp)
c.2941A>G (p.Asn981Asp)
n.3005A>G
c.*782A>G (n.*782A>G)
c.3001A>G (p.Asn1001Asp)
n.3051A>G
c.3253A>G (p.Asn1085Asp)
c.3154A>G (p.Asn1052Asp)
c.3568A>G (p.Asn1190Asp)
16g.9764132T>GCA394707921GRIN2Ac.3412A>C (p.Asn1138His)
c.2941A>C (p.Asn981His)
n.3005A>C
c.*782A>C (n.*782A>C)
c.3001A>C (p.Asn1001His)
n.3051A>C
c.3253A>C (p.Asn1085His)
c.3154A>C (p.Asn1052His)
c.3568A>C (p.Asn1190His)
16g.9764133T>ACA394707923GRIN2Ac.3411A>T (p.Glu1137Asp)
c.2940A>T (p.Glu980Asp)
n.3004A>T
c.*781A>T (n.*781A>T)
c.3000A>T (p.Glu1000Asp)
n.3050A>T
c.3252A>T (p.Glu1084Asp)
c.3153A>T (p.Glu1051Asp)
c.3567A>T (p.Glu1189Asp)
16g.9764133T>CCA493692891GRIN2Ac.3411A>G (p.Glu1137=)
c.2940A>G (p.Glu980=)
n.3004A>G
c.*781A>G (n.*781A>G)
c.3000A>G (p.Glu1000=)
n.3050A>G
c.3252A>G (p.Glu1084=)
c.3153A>G (p.Glu1051=)
c.3567A>G (p.Glu1189=)
 dbSNP
16g.9764133T>GCA394707922GRIN2Ac.3411A>C (p.Glu1137Asp)
c.2940A>C (p.Glu980Asp)
n.3004A>C
c.*781A>C (n.*781A>C)
c.3000A>C (p.Glu1000Asp)
n.3050A>C
c.3252A>C (p.Glu1084Asp)
c.3153A>C (p.Glu1051Asp)
c.3567A>C (p.Glu1189Asp)
 dbSNP
16g.9764133T=CA2206693067GRIN2Ac.3411A= (p.Glu1137=)
c.2940A= (p.Glu980=)
n.3004A=
c.*781A= (n.*781A=)
c.3000A= (p.Glu1000=)
n.3050A=
c.3252A= (p.Glu1084=)
c.3153A= (p.Glu1051=)
c.3567A= (p.Glu1189=)
16g.9764134T>ACA394707924GRIN2Ac.3410A>T (p.Glu1137Val)
c.2939A>T (p.Glu980Val)
n.3003A>T
c.*780A>T (n.*780A>T)
c.2999A>T (p.Glu1000Val)
n.3049A>T
c.3251A>T (p.Glu1084Val)
c.3152A>T (p.Glu1051Val)
c.3566A>T (p.Glu1189Val)
 ClinVar dbSNP gnomAD v2 gnomAD v4
16g.9764134T>CCA394707925GRIN2Ac.3410A>G (p.Glu1137Gly)
c.2939A>G (p.Glu980Gly)
n.3003A>G
c.*780A>G (n.*780A>G)
c.2999A>G (p.Glu1000Gly)
n.3049A>G
c.3251A>G (p.Glu1084Gly)
c.3152A>G (p.Glu1051Gly)
c.3566A>G (p.Glu1189Gly)
 dbSNP
16g.9764134T>GCA394707926GRIN2Ac.3410A>C (p.Glu1137Ala)
c.2939A>C (p.Glu980Ala)
n.3003A>C
c.*780A>C (n.*780A>C)
c.2999A>C (p.Glu1000Ala)
n.3049A>C
c.3251A>C (p.Glu1084Ala)
c.3152A>C (p.Glu1051Ala)
c.3566A>C (p.Glu1189Ala)
 dbSNP
16g.9764134T=CA2206693068GRIN2Ac.3410A= (p.Glu1137=)
c.2939A= (p.Glu980=)
n.3003A=
c.*780A= (n.*780A=)
c.2999A= (p.Glu1000=)
n.3049A=
c.3251A= (p.Glu1084=)
c.3152A= (p.Glu1051=)
c.3566A= (p.Glu1189=)
16g.9764135C>ACA394707927GRIN2Ac.3409G>T (p.Glu1137Ter)
c.2938G>T (p.Glu980Ter)
n.3002G>T
c.*779G>T (n.*779G>T)
c.2998G>T (p.Glu1000Ter)
n.3048G>T
c.3250G>T (p.Glu1084Ter)
c.3151G>T (p.Glu1051Ter)
c.3565G>T (p.Glu1189Ter)
 dbSNP
16g.9764135C=CA2206693069GRIN2Ac.3409G= (p.Glu1137=)
c.2938G= (p.Glu980=)
n.3002G=
c.*779G= (n.*779G=)
c.2998G= (p.Glu1000=)
n.3048G=
c.3250G= (p.Glu1084=)
c.3151G= (p.Glu1051=)
c.3565G= (p.Glu1189=)
16g.9764135C>GCA394707928GRIN2Ac.3409G>C (p.Glu1137Gln)
c.2938G>C (p.Glu980Gln)
n.3002G>C
c.*779G>C (n.*779G>C)
c.2998G>C (p.Glu1000Gln)
n.3048G>C
c.3250G>C (p.Glu1084Gln)
c.3151G>C (p.Glu1051Gln)
c.3565G>C (p.Glu1189Gln)
 dbSNP gnomAD v2 gnomAD v4
16g.9764135C>TCA394707929GRIN2Ac.3409G>A (p.Glu1137Lys)
c.2938G>A (p.Glu980Lys)
n.3002G>A
c.*779G>A (n.*779G>A)
c.2998G>A (p.Glu1000Lys)
n.3048G>A
c.3250G>A (p.Glu1084Lys)
c.3151G>A (p.Glu1051Lys)
c.3565G>A (p.Glu1189Lys)
 ClinVar dbSNP
16g.9764136A>CCA493692893GRIN2Ac.3408T>G (p.Val1136=)
c.2937T>G (p.Val979=)
n.3001T>G
c.*778T>G (n.*778T>G)
c.2997T>G (p.Val999=)
n.3047T>G
c.3249T>G (p.Val1083=)
c.3150T>G (p.Val1050=)
c.3564T>G (p.Val1188=)
16g.9764136A>GCA493692894GRIN2Ac.3408T>C (p.Val1136=)
c.2937T>C (p.Val979=)
n.3001T>C
c.*778T>C (n.*778T>C)
c.2997T>C (p.Val999=)
n.3047T>C
c.3249T>C (p.Val1083=)
c.3150T>C (p.Val1050=)
c.3564T>C (p.Val1188=)
 dbSNP
16g.9764136A>TCA493692895GRIN2Ac.3408T>A (p.Val1136=)
c.2937T>A (p.Val979=)
n.3001T>A
c.*778T>A (n.*778T>A)
c.2997T>A (p.Val999=)
n.3047T>A
c.3249T>A (p.Val1083=)
c.3150T>A (p.Val1050=)
c.3564T>A (p.Val1188=)
 dbSNP
16g.9764137A=CA2206693070GRIN2Ac.3407T= (p.Val1136=)
c.2936T= (p.Val979=)
n.3000T=
c.*777T= (n.*777T=)
c.2996T= (p.Val999=)
n.3046T=
c.3248T= (p.Val1083=)
c.3149T= (p.Val1050=)
c.3563T= (p.Val1188=)
16g.9764137A>CCA394707932GRIN2Ac.3407T>G (p.Val1136Gly)
c.2936T>G (p.Val979Gly)
n.3000T>G
c.*777T>G (n.*777T>G)
c.2996T>G (p.Val999Gly)
n.3046T>G
c.3248T>G (p.Val1083Gly)
c.3149T>G (p.Val1050Gly)
c.3563T>G (p.Val1188Gly)
 dbSNP
16g.9764137A>GCA394707930GRIN2Ac.3407T>C (p.Val1136Ala)
c.2936T>C (p.Val979Ala)
n.3000T>C
c.*777T>C (n.*777T>C)
c.2996T>C (p.Val999Ala)
n.3046T>C
c.3248T>C (p.Val1083Ala)
c.3149T>C (p.Val1050Ala)
c.3563T>C (p.Val1188Ala)
 dbSNP
16g.9764137A>TCA394707931GRIN2Ac.3407T>A (p.Val1136Asp)
c.2936T>A (p.Val979Asp)
n.3000T>A
c.*777T>A (n.*777T>A)
c.2996T>A (p.Val999Asp)
n.3046T>A
c.3248T>A (p.Val1083Asp)
c.3149T>A (p.Val1050Asp)
c.3563T>A (p.Val1188Asp)
 dbSNP
16g.9764138C>ACA394707933GRIN2Ac.3406G>T (p.Val1136Phe)
c.2935G>T (p.Val979Phe)
n.2999G>T
c.*776G>T (n.*776G>T)
c.2995G>T (p.Val999Phe)
n.3045G>T
c.3247G>T (p.Val1083Phe)
c.3148G>T (p.Val1050Phe)
c.3562G>T (p.Val1188Phe)
16g.9764138C>GCA394707934GRIN2Ac.3406G>C (p.Val1136Leu)
c.2935G>C (p.Val979Leu)
n.2999G>C
c.*776G>C (n.*776G>C)
c.2995G>C (p.Val999Leu)
n.3045G>C
c.3247G>C (p.Val1083Leu)
c.3148G>C (p.Val1050Leu)
c.3562G>C (p.Val1188Leu)
 dbSNP
16g.9764138C>TCA394707935GRIN2Ac.3406G>A (p.Val1136Ile)
c.2935G>A (p.Val979Ile)
n.2999G>A
c.*776G>A (n.*776G>A)
c.2995G>A (p.Val999Ile)
n.3045G>A
c.3247G>A (p.Val1083Ile)
c.3148G>A (p.Val1050Ile)
c.3562G>A (p.Val1188Ile)
 dbSNP
16g.9764139A>CCA394707936GRIN2Ac.3405T>G (p.Phe1135Leu)
c.2934T>G (p.Phe978Leu)
n.2998T>G
c.*775T>G (n.*775T>G)
c.2994T>G (p.Phe998Leu)
n.3044T>G
c.3246T>G (p.Phe1082Leu)
c.3147T>G (p.Phe1049Leu)
c.3561T>G (p.Phe1187Leu)
16g.9764139A>GCA493692900GRIN2Ac.3405T>C (p.Phe1135=)
c.2934T>C (p.Phe978=)
n.2998T>C
c.*775T>C (n.*775T>C)
c.2994T>C (p.Phe998=)
n.3044T>C
c.3246T>C (p.Phe1082=)
c.3147T>C (p.Phe1049=)
c.3561T>C (p.Phe1187=)
16g.9764139A>TCA394707937GRIN2Ac.3405T>A (p.Phe1135Leu)
c.2934T>A (p.Phe978Leu)
n.2998T>A
c.*775T>A (n.*775T>A)
c.2994T>A (p.Phe998Leu)
n.3044T>A
c.3246T>A (p.Phe1082Leu)
c.3147T>A (p.Phe1049Leu)
c.3561T>A (p.Phe1187Leu)
16g.9764140A>CCA394707938GRIN2Ac.3404T>G (p.Phe1135Cys)
c.2933T>G (p.Phe978Cys)
n.2997T>G
c.*774T>G (n.*774T>G)
c.2993T>G (p.Phe998Cys)
n.3043T>G
c.3245T>G (p.Phe1082Cys)
c.3146T>G (p.Phe1049Cys)
c.3560T>G (p.Phe1187Cys)
16g.9764140A>GCA394707940GRIN2Ac.3404T>C (p.Phe1135Ser)
c.2933T>C (p.Phe978Ser)
n.2997T>C
c.*774T>C (n.*774T>C)
c.2993T>C (p.Phe998Ser)
n.3043T>C
c.3245T>C (p.Phe1082Ser)
c.3146T>C (p.Phe1049Ser)
c.3560T>C (p.Phe1187Ser)
16g.9764140A>TCA394707939GRIN2Ac.3404T>A (p.Phe1135Tyr)
c.2933T>A (p.Phe978Tyr)
n.2997T>A
c.*774T>A (n.*774T>A)
c.2993T>A (p.Phe998Tyr)
n.3043T>A
c.3245T>A (p.Phe1082Tyr)
c.3146T>A (p.Phe1049Tyr)
c.3560T>A (p.Phe1187Tyr)
 dbSNP
16g.9764141A>CCA394707941GRIN2Ac.3403T>G (p.Phe1135Val)
c.2932T>G (p.Phe978Val)
n.2996T>G
c.*773T>G (n.*773T>G)
c.2992T>G (p.Phe998Val)
n.3042T>G
c.3244T>G (p.Phe1082Val)
c.3145T>G (p.Phe1049Val)
c.3559T>G (p.Phe1187Val)
16g.9764141A>GCA394707942GRIN2Ac.3403T>C (p.Phe1135Leu)
c.2932T>C (p.Phe978Leu)
n.2996T>C
c.*773T>C (n.*773T>C)
c.2992T>C (p.Phe998Leu)
n.3042T>C
c.3244T>C (p.Phe1082Leu)
c.3145T>C (p.Phe1049Leu)
c.3559T>C (p.Phe1187Leu)
16g.9764141A>TCA394707943GRIN2Ac.3403T>A (p.Phe1135Ile)
c.2932T>A (p.Phe978Ile)
n.2996T>A
c.*773T>A (n.*773T>A)
c.2992T>A (p.Phe998Ile)
n.3042T>A
c.3244T>A (p.Phe1082Ile)
c.3145T>A (p.Phe1049Ile)
c.3559T>A (p.Phe1187Ile)
 dbSNP
16g.9764142C>ACA394707944GRIN2Ac.3402G>T (p.Gln1134His)
c.2931G>T (p.Gln977His)
n.2995G>T
c.*772G>T (n.*772G>T)
c.2991G>T (p.Gln997His)
n.3041G>T
c.3243G>T (p.Gln1081His)
c.3144G>T (p.Gln1048His)
c.3558G>T (p.Gln1186His)
16g.9764142C>GCA394707945GRIN2Ac.3402G>C (p.Gln1134His)
c.2931G>C (p.Gln977His)
n.2995G>C
c.*772G>C (n.*772G>C)
c.2991G>C (p.Gln997His)
n.3041G>C
c.3243G>C (p.Gln1081His)
c.3144G>C (p.Gln1048His)
c.3558G>C (p.Gln1186His)
 ClinVar dbSNP
16g.9764142C>TCA493692904GRIN2Ac.3402G>A (p.Gln1134=)
c.2931G>A (p.Gln977=)
n.2995G>A
c.*772G>A (n.*772G>A)
c.2991G>A (p.Gln997=)
n.3041G>A
c.3243G>A (p.Gln1081=)
c.3144G>A (p.Gln1048=)
c.3558G>A (p.Gln1186=)
 dbSNP
16g.9764143T>ACA394707948GRIN2Ac.3401A>T (p.Gln1134Leu)
c.2930A>T (p.Gln977Leu)
n.2994A>T
c.*771A>T (n.*771A>T)
c.2990A>T (p.Gln997Leu)
n.3040A>T
c.3242A>T (p.Gln1081Leu)
c.3143A>T (p.Gln1048Leu)
c.3557A>T (p.Gln1186Leu)
 dbSNP
16g.9764143T>CCA394707947GRIN2Ac.3401A>G (p.Gln1134Arg)
c.2930A>G (p.Gln977Arg)
n.2994A>G
c.*771A>G (n.*771A>G)
c.2990A>G (p.Gln997Arg)
n.3040A>G
c.3242A>G (p.Gln1081Arg)
c.3143A>G (p.Gln1048Arg)
c.3557A>G (p.Gln1186Arg)
16g.9764143T>GCA394707946GRIN2Ac.3401A>C (p.Gln1134Pro)
c.2930A>C (p.Gln977Pro)
n.2994A>C
c.*771A>C (n.*771A>C)
c.2990A>C (p.Gln997Pro)
n.3040A>C
c.3242A>C (p.Gln1081Pro)
c.3143A>C (p.Gln1048Pro)
c.3557A>C (p.Gln1186Pro)
16g.9764144G>ACA394707949GRIN2Ac.3400C>T (p.Gln1134Ter)
c.2929C>T (p.Gln977Ter)
n.2993C>T
c.*770C>T (n.*770C>T)
c.2989C>T (p.Gln997Ter)
n.3039C>T
c.3241C>T (p.Gln1081Ter)
c.3142C>T (p.Gln1048Ter)
c.3556C>T (p.Gln1186Ter)
 dbSNP
16g.9764144G>CCA394707950GRIN2Ac.3400C>G (p.Gln1134Glu)
c.2929C>G (p.Gln977Glu)
n.2993C>G
c.*770C>G (n.*770C>G)
c.2989C>G (p.Gln997Glu)
n.3039C>G
c.3241C>G (p.Gln1081Glu)
c.3142C>G (p.Gln1048Glu)
c.3556C>G (p.Gln1186Glu)
 dbSNP
16g.9764144G=CA2206693071GRIN2Ac.3400C= (p.Gln1134=)
c.2929C= (p.Gln977=)
n.2993C=
c.*770C= (n.*770C=)
c.2989C= (p.Gln997=)
n.3039C=
c.3241C= (p.Gln1081=)
c.3142C= (p.Gln1048=)
c.3556C= (p.Gln1186=)
16g.9764144G>TCA7896323GRIN2Ac.3400C>A (p.Gln1134Lys)
c.2929C>A (p.Gln977Lys)
n.2993C>A
c.*770C>A (n.*770C>A)
c.2989C>A (p.Gln997Lys)
n.3039C>A
c.3241C>A (p.Gln1081Lys)
c.3142C>A (p.Gln1048Lys)
c.3556C>A (p.Gln1186Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.9764145G>ACA493692910GRIN2Ac.3399C>T (p.Pro1133=)
c.2928C>T (p.Pro976=)
n.2992C>T
c.*769C>T (n.*769C>T)
c.2988C>T (p.Pro996=)
n.3038C>T
c.3240C>T (p.Pro1080=)
c.3141C>T (p.Pro1047=)
c.3555C>T (p.Pro1185=)
 dbSNP
16g.9764145G>CCA493692911GRIN2Ac.3399C>G (p.Pro1133=)
c.2928C>G (p.Pro976=)
n.2992C>G
c.*769C>G (n.*769C>G)
c.2988C>G (p.Pro996=)
n.3038C>G
c.3240C>G (p.Pro1080=)
c.3141C>G (p.Pro1047=)
c.3555C>G (p.Pro1185=)
 dbSNP
16g.9764145G=CA2206693072GRIN2Ac.3399C= (p.Pro1133=)
c.2928C= (p.Pro976=)
n.2992C=
c.*769C= (n.*769C=)
c.2988C= (p.Pro996=)
n.3038C=
c.3240C= (p.Pro1080=)
c.3141C= (p.Pro1047=)
c.3555C= (p.Pro1185=)
16g.9764145G>TCA493692912GRIN2Ac.3399C>A (p.Pro1133=)
c.2928C>A (p.Pro976=)
n.2992C>A
c.*769C>A (n.*769C>A)
c.2988C>A (p.Pro996=)
n.3038C>A
c.3240C>A (p.Pro1080=)
c.3141C>A (p.Pro1047=)
c.3555C>A (p.Pro1185=)
 dbSNP COSMIC
16g.9764146G>ACA394707951GRIN2Ac.3398C>T (p.Pro1133Leu)
c.2927C>T (p.Pro976Leu)
n.2991C>T
c.*768C>T (n.*768C>T)
c.2987C>T (p.Pro996Leu)
n.3037C>T
c.3239C>T (p.Pro1080Leu)
c.3140C>T (p.Pro1047Leu)
c.3554C>T (p.Pro1185Leu)
 dbSNP
16g.9764146G>CCA394707952GRIN2Ac.3398C>G (p.Pro1133Arg)
c.2927C>G (p.Pro976Arg)
n.2991C>G
c.*768C>G (n.*768C>G)
c.2987C>G (p.Pro996Arg)
n.3037C>G
c.3239C>G (p.Pro1080Arg)
c.3140C>G (p.Pro1047Arg)
c.3554C>G (p.Pro1185Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v4
16g.9764146G=CA2206693073GRIN2Ac.3398C= (p.Pro1133=)
c.2927C= (p.Pro976=)
n.2991C=
c.*768C= (n.*768C=)
c.2987C= (p.Pro996=)
n.3037C=
c.3239C= (p.Pro1080=)
c.3140C= (p.Pro1047=)
c.3554C= (p.Pro1185=)
16g.9764146G>TCA394707953GRIN2Ac.3398C>A (p.Pro1133His)
c.2927C>A (p.Pro976His)
n.2991C>A
c.*768C>A (n.*768C>A)
c.2987C>A (p.Pro996His)
n.3037C>A
c.3239C>A (p.Pro1080His)
c.3140C>A (p.Pro1047His)
c.3554C>A (p.Pro1185His)
 dbSNP
16g.9764147G>ACA394707954GRIN2Ac.3397C>T (p.Pro1133Ser)
c.2926C>T (p.Pro976Ser)
n.2990C>T
c.*767C>T (n.*767C>T)
c.2986C>T (p.Pro996Ser)
n.3036C>T
c.3238C>T (p.Pro1080Ser)
c.3139C>T (p.Pro1047Ser)
c.3553C>T (p.Pro1185Ser)
 dbSNP gnomAD v4 COSMIC
16g.9764147G>CCA394707956GRIN2Ac.3397C>G (p.Pro1133Ala)
c.2926C>G (p.Pro976Ala)
n.2990C>G
c.*767C>G (n.*767C>G)
c.2986C>G (p.Pro996Ala)
n.3036C>G
c.3238C>G (p.Pro1080Ala)
c.3139C>G (p.Pro1047Ala)
c.3553C>G (p.Pro1185Ala)
 dbSNP
16g.9764147G=CA2206693074GRIN2Ac.3397C= (p.Pro1133=)
c.2926C= (p.Pro976=)
n.2990C=
c.*767C= (n.*767C=)
c.2986C= (p.Pro996=)
n.3036C=
c.3238C= (p.Pro1080=)
c.3139C= (p.Pro1047=)
c.3553C= (p.Pro1185=)
16g.9764147G>TCA394707955GRIN2Ac.3397C>A (p.Pro1133Thr)
c.2926C>A (p.Pro976Thr)
n.2990C>A
c.*767C>A (n.*767C>A)
c.2986C>A (p.Pro996Thr)
n.3036C>A
c.3238C>A (p.Pro1080Thr)
c.3139C>A (p.Pro1047Thr)
c.3553C>A (p.Pro1185Thr)
16g.9764148T>ACA493692913GRIN2Ac.3396A>T (p.Pro1132=)
c.2925A>T (p.Pro975=)
n.2989A>T
c.*766A>T (n.*766A>T)
c.2985A>T (p.Pro995=)
n.3035A>T
c.3237A>T (p.Pro1079=)
c.3138A>T (p.Pro1046=)
c.3552A>T (p.Pro1184=)
16g.9764148T>CCA493692914GRIN2Ac.3396A>G (p.Pro1132=)
c.2925A>G (p.Pro975=)
n.2989A>G
c.*766A>G (n.*766A>G)
c.2985A>G (p.Pro995=)
n.3035A>G
c.3237A>G (p.Pro1079=)
c.3138A>G (p.Pro1046=)
c.3552A>G (p.Pro1184=)
16g.9764148T>GCA493692916GRIN2Ac.3396A>C (p.Pro1132=)
c.2925A>C (p.Pro975=)
n.2989A>C
c.*766A>C (n.*766A>C)
c.2985A>C (p.Pro995=)
n.3035A>C
c.3237A>C (p.Pro1079=)
c.3138A>C (p.Pro1046=)
c.3552A>C (p.Pro1184=)
16g.9764149G>ACA394707957GRIN2Ac.3395C>T (p.Pro1132Leu)
c.2924C>T (p.Pro975Leu)
n.2988C>T
c.*765C>T (n.*765C>T)
c.2984C>T (p.Pro995Leu)
n.3034C>T
c.3236C>T (p.Pro1079Leu)
c.3137C>T (p.Pro1046Leu)
c.3551C>T (p.Pro1184Leu)
 dbSNP gnomAD v4 COSMIC
16g.9764149G>CCA394707958GRIN2Ac.3395C>G (p.Pro1132Arg)
c.2924C>G (p.Pro975Arg)
n.2988C>G
c.*765C>G (n.*765C>G)
c.2984C>G (p.Pro995Arg)
n.3034C>G
c.3236C>G (p.Pro1079Arg)
c.3137C>G (p.Pro1046Arg)
c.3551C>G (p.Pro1184Arg)
 dbSNP
16g.9764149G>TCA394707959GRIN2Ac.3395C>A (p.Pro1132Gln)
c.2924C>A (p.Pro975Gln)
n.2988C>A
c.*765C>A (n.*765C>A)
c.2984C>A (p.Pro995Gln)
n.3034C>A
c.3236C>A (p.Pro1079Gln)
c.3137C>A (p.Pro1046Gln)
c.3551C>A (p.Pro1184Gln)
 dbSNP
16g.9764150G>ACA394707960GRIN2Ac.3394C>T (p.Pro1132Ser)
c.2923C>T (p.Pro975Ser)
n.2987C>T
c.*764C>T (n.*764C>T)
c.2983C>T (p.Pro995Ser)
n.3033C>T
c.3235C>T (p.Pro1079Ser)
c.3136C>T (p.Pro1046Ser)
c.3550C>T (p.Pro1184Ser)
 dbSNP COSMIC
16g.9764150G>CCA394707961GRIN2Ac.3394C>G (p.Pro1132Ala)
c.2923C>G (p.Pro975Ala)
n.2987C>G
c.*764C>G (n.*764C>G)
c.2983C>G (p.Pro995Ala)
n.3033C>G
c.3235C>G (p.Pro1079Ala)
c.3136C>G (p.Pro1046Ala)
c.3550C>G (p.Pro1184Ala)
 dbSNP
16g.9764150G=CA2206693075GRIN2Ac.3394C= (p.Pro1132=)
c.2923C= (p.Pro975=)
n.2987C=
c.*764C= (n.*764C=)
c.2983C= (p.Pro995=)
n.3033C=
c.3235C= (p.Pro1079=)
c.3136C= (p.Pro1046=)
c.3550C= (p.Pro1184=)
16g.9764150G>TCA7896324GRIN2Ac.3394C>A (p.Pro1132Thr)
c.2923C>A (p.Pro975Thr)
n.2987C>A
c.*764C>A (n.*764C>A)
c.2983C>A (p.Pro995Thr)
n.3033C>A
c.3235C>A (p.Pro1079Thr)
c.3136C>A (p.Pro1046Thr)
c.3550C>A (p.Pro1184Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.9764151A=CA2206693076GRIN2Ac.3393T= (p.Asp1131=)
c.2922T= (p.Asp974=)
n.2986T=
c.*763T= (n.*763T=)
c.2982T= (p.Asp994=)
n.3032T=
c.3234T= (p.Asp1078=)
c.3135T= (p.Asp1045=)
c.3549T= (p.Asp1183=)
16g.9764151A>CCA394707962GRIN2Ac.3393T>G (p.Asp1131Glu)
c.2922T>G (p.Asp974Glu)
n.2986T>G
c.*763T>G (n.*763T>G)
c.2982T>G (p.Asp994Glu)
n.3032T>G
c.3234T>G (p.Asp1078Glu)
c.3135T>G (p.Asp1045Glu)
c.3549T>G (p.Asp1183Glu)
 ClinVar dbSNP gnomAD v3 gnomAD v4
16g.9764151A>GCA493692921GRIN2Ac.3393T>C (p.Asp1131=)
c.2922T>C (p.Asp974=)
n.2986T>C
c.*763T>C (n.*763T>C)
c.2982T>C (p.Asp994=)
n.3032T>C
c.3234T>C (p.Asp1078=)
c.3135T>C (p.Asp1045=)
c.3549T>C (p.Asp1183=)
16g.9764151A>TCA394707963GRIN2Ac.3393T>A (p.Asp1131Glu)
c.2922T>A (p.Asp974Glu)
n.2986T>A
c.*763T>A (n.*763T>A)
c.2982T>A (p.Asp994Glu)
n.3032T>A
c.3234T>A (p.Asp1078Glu)
c.3135T>A (p.Asp1045Glu)
c.3549T>A (p.Asp1183Glu)
 dbSNP gnomAD v4
16g.9764152T>ACA394707964GRIN2Ac.3392A>T (p.Asp1131Val)
c.2921A>T (p.Asp974Val)
n.2985A>T
c.*762A>T (n.*762A>T)
c.2981A>T (p.Asp994Val)
n.3031A>T
c.3233A>T (p.Asp1078Val)
c.3134A>T (p.Asp1045Val)
c.3548A>T (p.Asp1183Val)
 dbSNP
16g.9764152T>CCA394707965GRIN2Ac.3392A>G (p.Asp1131Gly)
c.2921A>G (p.Asp974Gly)
n.2985A>G
c.*762A>G (n.*762A>G)
c.2981A>G (p.Asp994Gly)
n.3031A>G
c.3233A>G (p.Asp1078Gly)
c.3134A>G (p.Asp1045Gly)
c.3548A>G (p.Asp1183Gly)
16g.9764152T>GCA394707966GRIN2Ac.3392A>C (p.Asp1131Ala)
c.2921A>C (p.Asp974Ala)
n.2985A>C
c.*762A>C (n.*762A>C)
c.2981A>C (p.Asp994Ala)
n.3031A>C
c.3233A>C (p.Asp1078Ala)
c.3134A>C (p.Asp1045Ala)
c.3548A>C (p.Asp1183Ala)
 dbSNP
16g.9764153C>ACA394707968GRIN2Ac.3391G>T (p.Asp1131Tyr)
c.2920G>T (p.Asp974Tyr)
n.2984G>T
c.*761G>T (n.*761G>T)
c.2980G>T (p.Asp994Tyr)
n.3030G>T
c.3232G>T (p.Asp1078Tyr)
c.3133G>T (p.Asp1045Tyr)
c.3547G>T (p.Asp1183Tyr)
 ClinVar dbSNP gnomAD v2 gnomAD v4
16g.9764153C=CA2206693077GRIN2Ac.3391G= (p.Asp1131=)
c.2920G= (p.Asp974=)
n.2984G=
c.*761G= (n.*761G=)
c.2980G= (p.Asp994=)
n.3030G=
c.3232G= (p.Asp1078=)
c.3133G= (p.Asp1045=)
c.3547G= (p.Asp1183=)
16g.9764153C>GCA394707969GRIN2Ac.3391G>C (p.Asp1131His)
c.2920G>C (p.Asp974His)
n.2984G>C
c.*761G>C (n.*761G>C)
c.2980G>C (p.Asp994His)
n.3030G>C
c.3232G>C (p.Asp1078His)
c.3133G>C (p.Asp1045His)
c.3547G>C (p.Asp1183His)
 ClinVar dbSNP gnomAD v4
16g.9764153C>TCA394707967GRIN2Ac.3391G>A (p.Asp1131Asn)
c.2920G>A (p.Asp974Asn)
n.2984G>A
c.*761G>A (n.*761G>A)
c.2980G>A (p.Asp994Asn)
n.3030G>A
c.3232G>A (p.Asp1078Asn)
c.3133G>A (p.Asp1045Asn)
c.3547G>A (p.Asp1183Asn)
 dbSNP
16g.9764154T>ACA394707970GRIN2Ac.3390A>T (p.Leu1130Phe)
c.2919A>T (p.Leu973Phe)
n.2983A>T
c.*760A>T (n.*760A>T)
c.2979A>T (p.Leu993Phe)
n.3029A>T
c.3231A>T (p.Leu1077Phe)
c.3132A>T (p.Leu1044Phe)
c.3546A>T (p.Leu1182Phe)
16g.9764154T>CCA493692925GRIN2Ac.3390A>G (p.Leu1130=)
c.2919A>G (p.Leu973=)
n.2983A>G
c.*760A>G (n.*760A>G)
c.2979A>G (p.Leu993=)
n.3029A>G
c.3231A>G (p.Leu1077=)
c.3132A>G (p.Leu1044=)
c.3546A>G (p.Leu1182=)
16g.9764154T>GCA394707971GRIN2Ac.3390A>C (p.Leu1130Phe)
c.2919A>C (p.Leu973Phe)
n.2983A>C
c.*760A>C (n.*760A>C)
c.2979A>C (p.Leu993Phe)
n.3029A>C
c.3231A>C (p.Leu1077Phe)
c.3132A>C (p.Leu1044Phe)
c.3546A>C (p.Leu1182Phe)
 ClinVar dbSNP
16g.9764155A>CCA394707972GRIN2Ac.3389T>G (p.Leu1130Ter)
c.2918T>G (p.Leu973Ter)
n.2982T>G
c.*759T>G (n.*759T>G)
c.2978T>G (p.Leu993Ter)
n.3028T>G
c.3230T>G (p.Leu1077Ter)
c.3131T>G (p.Leu1044Ter)
c.3545T>G (p.Leu1182Ter)
16g.9764155A>GCA394707973GRIN2Ac.3389T>C (p.Leu1130Ser)
c.2918T>C (p.Leu973Ser)
n.2982T>C
c.*759T>C (n.*759T>C)
c.2978T>C (p.Leu993Ser)
n.3028T>C
c.3230T>C (p.Leu1077Ser)
c.3131T>C (p.Leu1044Ser)
c.3545T>C (p.Leu1182Ser)
16g.9764155A>TCA394707974GRIN2Ac.3389T>A (p.Leu1130Ter)
c.2918T>A (p.Leu973Ter)
n.2982T>A
c.*759T>A (n.*759T>A)
c.2978T>A (p.Leu993Ter)
n.3028T>A
c.3230T>A (p.Leu1077Ter)
c.3131T>A (p.Leu1044Ter)
c.3545T>A (p.Leu1182Ter)
 dbSNP
16g.9764156A>CCA394707975GRIN2Ac.3388T>G (p.Leu1130Val)
c.2917T>G (p.Leu973Val)
n.2981T>G
c.*758T>G (n.*758T>G)
c.2977T>G (p.Leu993Val)
n.3027T>G
c.3229T>G (p.Leu1077Val)
c.3130T>G (p.Leu1044Val)
c.3544T>G (p.Leu1182Val)
16g.9764156A>GCA493692929GRIN2Ac.3388T>C (p.Leu1130=)
c.2917T>C (p.Leu973=)
n.2981T>C
c.*758T>C (n.*758T>C)
c.2977T>C (p.Leu993=)
n.3027T>C
c.3229T>C (p.Leu1077=)
c.3130T>C (p.Leu1044=)
c.3544T>C (p.Leu1182=)
 ClinVar gnomAD v4
16g.9764156A>TCA394707976GRIN2Ac.3388T>A (p.Leu1130Ile)
c.2917T>A (p.Leu973Ile)
n.2981T>A
c.*758T>A (n.*758T>A)
c.2977T>A (p.Leu993Ile)
n.3027T>A
c.3229T>A (p.Leu1077Ile)
c.3130T>A (p.Leu1044Ile)
c.3544T>A (p.Leu1182Ile)
 dbSNP
16g.9764157G>ACA493692930GRIN2Ac.3387C>T (p.His1129=)
c.2916C>T (p.His972=)
n.2980C>T
c.*757C>T (n.*757C>T)
c.2976C>T (p.His992=)
n.3026C>T
c.3228C>T (p.His1076=)
c.3129C>T (p.His1043=)
c.3543C>T (p.His1181=)
 ClinVar dbSNP
16g.9764157G>CCA394707977GRIN2Ac.3387C>G (p.His1129Gln)
c.2916C>G (p.His972Gln)
n.2980C>G
c.*757C>G (n.*757C>G)
c.2976C>G (p.His992Gln)
n.3026C>G
c.3228C>G (p.His1076Gln)
c.3129C>G (p.His1043Gln)
c.3543C>G (p.His1181Gln)
 ClinVar dbSNP
16g.9764157G=CA2206693078GRIN2Ac.3387C= (p.His1129=)
c.2916C= (p.His972=)
n.2980C=
c.*757C= (n.*757C=)
c.2976C= (p.His992=)
n.3026C=
c.3228C= (p.His1076=)
c.3129C= (p.His1043=)
c.3543C= (p.His1181=)
16g.9764157G>TCA394707978GRIN2Ac.3387C>A (p.His1129Gln)
c.2916C>A (p.His972Gln)
n.2980C>A
c.*757C>A (n.*757C>A)
c.2976C>A (p.His992Gln)
n.3026C>A
c.3228C>A (p.His1076Gln)
c.3129C>A (p.His1043Gln)
c.3543C>A (p.His1181Gln)
 gnomAD v4
16g.9764158T>ACA394707979GRIN2Ac.3386A>T (p.His1129Leu)
c.2915A>T (p.His972Leu)
n.2979A>T
c.*756A>T (n.*756A>T)
c.2975A>T (p.His992Leu)
n.3025A>T
c.3227A>T (p.His1076Leu)
c.3128A>T (p.His1043Leu)
c.3542A>T (p.His1181Leu)
 dbSNP gnomAD v3 gnomAD v4
16g.9764158T>CCA7896325GRIN2Ac.3386A>G (p.His1129Arg)
c.2915A>G (p.His972Arg)
n.2979A>G
c.*756A>G (n.*756A>G)
c.2975A>G (p.His992Arg)
n.3025A>G
c.3227A>G (p.His1076Arg)
c.3128A>G (p.His1043Arg)
c.3542A>G (p.His1181Arg)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.9764158T>GCA394707980GRIN2Ac.3386A>C (p.His1129Pro)
c.2915A>C (p.His972Pro)
n.2979A>C
c.*756A>C (n.*756A>C)
c.2975A>C (p.His992Pro)
n.3025A>C
c.3227A>C (p.His1076Pro)
c.3128A>C (p.His1043Pro)
c.3542A>C (p.His1181Pro)
 dbSNP
16g.9764158T=CA2206693079GRIN2Ac.3386A= (p.His1129=)
c.2915A= (p.His972=)
n.2979A=
c.*756A= (n.*756A=)
c.2975A= (p.His992=)
n.3025A=
c.3227A= (p.His1076=)
c.3128A= (p.His1043=)
c.3542A= (p.His1181=)
16g.9764159G>ACA394707981GRIN2Ac.3385C>T (p.His1129Tyr)
c.2914C>T (p.His972Tyr)
n.2978C>T
c.*755C>T (n.*755C>T)
c.2974C>T (p.His992Tyr)
n.3024C>T
c.3226C>T (p.His1076Tyr)
c.3127C>T (p.His1043Tyr)
c.3541C>T (p.His1181Tyr)
 dbSNP COSMIC
16g.9764159G>CCA394707982GRIN2Ac.3385C>G (p.His1129Asp)
c.2914C>G (p.His972Asp)
n.2978C>G
c.*755C>G (n.*755C>G)
c.2974C>G (p.His992Asp)
n.3024C>G
c.3226C>G (p.His1076Asp)
c.3127C>G (p.His1043Asp)
c.3541C>G (p.His1181Asp)
 dbSNP
16g.9764159G>TCA394707983GRIN2Ac.3385C>A (p.His1129Asn)
c.2914C>A (p.His972Asn)
n.2978C>A
c.*755C>A (n.*755C>A)
c.2974C>A (p.His992Asn)
n.3024C>A
c.3226C>A (p.His1076Asn)
c.3127C>A (p.His1043Asn)
c.3541C>A (p.His1181Asn)
16g.9764160G>ACA493692934GRIN2Ac.3384C>T (p.Phe1128=)
c.2913C>T (p.Phe971=)
n.2977C>T
c.*754C>T (n.*754C>T)
c.2973C>T (p.Phe991=)
n.3023C>T
c.3225C>T (p.Phe1075=)
c.3126C>T (p.Phe1042=)
c.3540C>T (p.Phe1180=)
 ClinVar dbSNP gnomAD v4 COSMIC
16g.9764160G>CCA394707985GRIN2Ac.3384C>G (p.Phe1128Leu)
c.2913C>G (p.Phe971Leu)
n.2977C>G
c.*754C>G (n.*754C>G)
c.2973C>G (p.Phe991Leu)
n.3023C>G
c.3225C>G (p.Phe1075Leu)
c.3126C>G (p.Phe1042Leu)
c.3540C>G (p.Phe1180Leu)
 dbSNP
16g.9764160G=CA2206693080GRIN2Ac.3384C= (p.Phe1128=)
c.2913C= (p.Phe971=)
n.2977C=
c.*754C= (n.*754C=)
c.2973C= (p.Phe991=)
n.3023C=
c.3225C= (p.Phe1075=)
c.3126C= (p.Phe1042=)
c.3540C= (p.Phe1180=)
16g.9764160G>TCA394707984GRIN2Ac.3384C>A (p.Phe1128Leu)
c.2913C>A (p.Phe971Leu)
n.2977C>A
c.*754C>A (n.*754C>A)
c.2973C>A (p.Phe991Leu)
n.3023C>A
c.3225C>A (p.Phe1075Leu)
c.3126C>A (p.Phe1042Leu)
c.3540C>A (p.Phe1180Leu)
 dbSNP gnomAD v3 gnomAD v4
16g.9764161A>CCA394707986GRIN2Ac.3383T>G (p.Phe1128Cys)
c.2912T>G (p.Phe971Cys)
n.2976T>G
c.*753T>G (n.*753T>G)
c.2972T>G (p.Phe991Cys)
n.3022T>G
c.3224T>G (p.Phe1075Cys)
c.3125T>G (p.Phe1042Cys)
c.3539T>G (p.Phe1180Cys)
16g.9764161A>GCA394707987GRIN2Ac.3383T>C (p.Phe1128Ser)
c.2912T>C (p.Phe971Ser)
n.2976T>C
c.*753T>C (n.*753T>C)
c.2972T>C (p.Phe991Ser)
n.3022T>C
c.3224T>C (p.Phe1075Ser)
c.3125T>C (p.Phe1042Ser)
c.3539T>C (p.Phe1180Ser)
 dbSNP
16g.9764161A>TCA394707988GRIN2Ac.3383T>A (p.Phe1128Tyr)
c.2912T>A (p.Phe971Tyr)
n.2976T>A
c.*753T>A (n.*753T>A)
c.2972T>A (p.Phe991Tyr)
n.3022T>A
c.3224T>A (p.Phe1075Tyr)
c.3125T>A (p.Phe1042Tyr)
c.3539T>A (p.Phe1180Tyr)
16g.9764162A>CCA394707990GRIN2Ac.3382T>G (p.Phe1128Val)
c.2911T>G (p.Phe971Val)
n.2975T>G
c.*752T>G (n.*752T>G)
c.2971T>G (p.Phe991Val)
n.3021T>G
c.3223T>G (p.Phe1075Val)
c.3124T>G (p.Phe1042Val)
c.3538T>G (p.Phe1180Val)
16g.9764162A>GCA394707991GRIN2Ac.3382T>C (p.Phe1128Leu)
c.2911T>C (p.Phe971Leu)
n.2975T>C
c.*752T>C (n.*752T>C)
c.2971T>C (p.Phe991Leu)
n.3021T>C
c.3223T>C (p.Phe1075Leu)
c.3124T>C (p.Phe1042Leu)
c.3538T>C (p.Phe1180Leu)
 dbSNP
16g.9764162A>TCA394707992GRIN2Ac.3382T>A (p.Phe1128Ile)
c.2911T>A (p.Phe971Ile)
n.2975T>A
c.*752T>A (n.*752T>A)
c.2971T>A (p.Phe991Ile)
n.3021T>A
c.3223T>A (p.Phe1075Ile)
c.3124T>A (p.Phe1042Ile)
c.3538T>A (p.Phe1180Ile)
 dbSNP
16g.9764163A>CCA493692936GRIN2Ac.3381T>G (p.Gly1127=)
c.2910T>G (p.Gly970=)
n.2974T>G
c.*751T>G (n.*751T>G)
c.2970T>G (p.Gly990=)
n.3020T>G
c.3222T>G (p.Gly1074=)
c.3123T>G (p.Gly1041=)
c.3537T>G (p.Gly1179=)
16g.9764163A>GCA493692938GRIN2Ac.3381T>C (p.Gly1127=)
c.2910T>C (p.Gly970=)
n.2974T>C
c.*751T>C (n.*751T>C)
c.2970T>C (p.Gly990=)
n.3020T>C
c.3222T>C (p.Gly1074=)
c.3123T>C (p.Gly1041=)
c.3537T>C (p.Gly1179=)
 gnomAD v4
16g.9764163A>TCA493692940GRIN2Ac.3381T>A (p.Gly1127=)
c.2910T>A (p.Gly970=)
n.2974T>A
c.*751T>A (n.*751T>A)
c.2970T>A (p.Gly990=)
n.3020T>A
c.3222T>A (p.Gly1074=)
c.3123T>A (p.Gly1041=)
c.3537T>A (p.Gly1179=)
16g.9764164C>ACA394707993GRIN2Ac.3380G>T (p.Gly1127Val)
c.2909G>T (p.Gly970Val)
n.2973G>T
c.*750G>T (n.*750G>T)
c.2969G>T (p.Gly990Val)
n.3019G>T
c.3221G>T (p.Gly1074Val)
c.3122G>T (p.Gly1041Val)
c.3536G>T (p.Gly1179Val)
 dbSNP
16g.9764164C>GCA394707994GRIN2Ac.3380G>C (p.Gly1127Ala)
c.2909G>C (p.Gly970Ala)
n.2973G>C
c.*750G>C (n.*750G>C)
c.2969G>C (p.Gly990Ala)
n.3019G>C
c.3221G>C (p.Gly1074Ala)
c.3122G>C (p.Gly1041Ala)
c.3536G>C (p.Gly1179Ala)
 dbSNP gnomAD v4
16g.9764164C>TCA394707995GRIN2Ac.3380G>A (p.Gly1127Asp)
c.2909G>A (p.Gly970Asp)
n.2973G>A
c.*750G>A (n.*750G>A)
c.2969G>A (p.Gly990Asp)
n.3019G>A
c.3221G>A (p.Gly1074Asp)
c.3122G>A (p.Gly1041Asp)
c.3536G>A (p.Gly1179Asp)
16g.9764165C>ACA394707996GRIN2Ac.3379G>T (p.Gly1127Cys)
c.2908G>T (p.Gly970Cys)
n.2972G>T
c.*749G>T (n.*749G>T)
c.2968G>T (p.Gly990Cys)
n.3018G>T
c.3220G>T (p.Gly1074Cys)
c.3121G>T (p.Gly1041Cys)
c.3535G>T (p.Gly1179Cys)
 COSMIC
16g.9764165C=CA2206693081GRIN2Ac.3379G= (p.Gly1127=)
c.2908G= (p.Gly970=)
n.2972G=
c.*749G= (n.*749G=)
c.2968G= (p.Gly990=)
n.3018G=
c.3220G= (p.Gly1074=)
c.3121G= (p.Gly1041=)
c.3535G= (p.Gly1179=)
16g.9764165C>GCA394707997GRIN2Ac.3379G>C (p.Gly1127Arg)
c.2908G>C (p.Gly970Arg)
n.2972G>C
c.*749G>C (n.*749G>C)
c.2968G>C (p.Gly990Arg)
n.3018G>C
c.3220G>C (p.Gly1074Arg)
c.3121G>C (p.Gly1041Arg)
c.3535G>C (p.Gly1179Arg)
 ClinVar dbSNP
16g.9764165C>TCA394707998GRIN2Ac.3379G>A (p.Gly1127Ser)
c.2908G>A (p.Gly970Ser)
n.2972G>A
c.*749G>A (n.*749G>A)
c.2968G>A (p.Gly990Ser)
n.3018G>A
c.3220G>A (p.Gly1074Ser)
c.3121G>A (p.Gly1041Ser)
c.3535G>A (p.Gly1179Ser)
 dbSNP gnomAD v2
16g.9764166A=CA2206693082GRIN2Ac.3378T= (p.Pro1126=)
c.2907T= (p.Pro969=)
n.2971T=
c.*748T= (n.*748T=)
c.2967T= (p.Pro989=)
n.3017T=
c.3219T= (p.Pro1073=)
c.3120T= (p.Pro1040=)
c.3534T= (p.Pro1178=)
16g.9764166A>CCA493692945GRIN2Ac.3378T>G (p.Pro1126=)
c.2907T>G (p.Pro969=)
n.2971T>G
c.*748T>G (n.*748T>G)
c.2967T>G (p.Pro989=)
n.3017T>G
c.3219T>G (p.Pro1073=)
c.3120T>G (p.Pro1040=)
c.3534T>G (p.Pro1178=)
 dbSNP
16g.9764166A>GCA7896326GRIN2Ac.3378T>C (p.Pro1126=)
c.2907T>C (p.Pro969=)
n.2971T>C
c.*748T>C (n.*748T>C)
c.2967T>C (p.Pro989=)
n.3017T>C
c.3219T>C (p.Pro1073=)
c.3120T>C (p.Pro1040=)
c.3534T>C (p.Pro1178=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.9764166A>TCA493692947GRIN2Ac.3378T>A (p.Pro1126=)
c.2907T>A (p.Pro969=)
n.2971T>A
c.*748T>A (n.*748T>A)
c.2967T>A (p.Pro989=)
n.3017T>A
c.3219T>A (p.Pro1073=)
c.3120T>A (p.Pro1040=)
c.3534T>A (p.Pro1178=)
 dbSNP
16g.9764167G>ACA394708001GRIN2Ac.3377C>T (p.Pro1126Leu)
c.2906C>T (p.Pro969Leu)
n.2970C>T
c.*747C>T (n.*747C>T)
c.2966C>T (p.Pro989Leu)
n.3016C>T
c.3218C>T (p.Pro1073Leu)
c.3119C>T (p.Pro1040Leu)
c.3533C>T (p.Pro1178Leu)
 ClinVar dbSNP
16g.9764167G>CCA394708000GRIN2Ac.3377C>G (p.Pro1126Arg)
c.2906C>G (p.Pro969Arg)
n.2970C>G
c.*747C>G (n.*747C>G)
c.2966C>G (p.Pro989Arg)
n.3016C>G
c.3218C>G (p.Pro1073Arg)
c.3119C>G (p.Pro1040Arg)
c.3533C>G (p.Pro1178Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v4
16g.9764167G=CA2206693083GRIN2Ac.3377C= (p.Pro1126=)
c.2906C= (p.Pro969=)
n.2970C=
c.*747C= (n.*747C=)
c.2966C= (p.Pro989=)
n.3016C=
c.3218C= (p.Pro1073=)
c.3119C= (p.Pro1040=)
c.3533C= (p.Pro1178=)
16g.9764167G>TCA394707999GRIN2Ac.3377C>A (p.Pro1126His)
c.2906C>A (p.Pro969His)
n.2970C>A
c.*747C>A (n.*747C>A)
c.2966C>A (p.Pro989His)
n.3016C>A
c.3218C>A (p.Pro1073His)
c.3119C>A (p.Pro1040His)
c.3533C>A (p.Pro1178His)
16g.9764168G>ACA394708003GRIN2Ac.3376C>T (p.Pro1126Ser)
c.2905C>T (p.Pro969Ser)
n.2969C>T
c.*746C>T (n.*746C>T)
c.2965C>T (p.Pro989Ser)
n.3015C>T
c.3217C>T (p.Pro1073Ser)
c.3118C>T (p.Pro1040Ser)
c.3532C>T (p.Pro1178Ser)
 dbSNP
16g.9764168G>CCA394708002GRIN2Ac.3376C>G (p.Pro1126Ala)
c.2905C>G (p.Pro969Ala)
n.2969C>G
c.*746C>G (n.*746C>G)
c.2965C>G (p.Pro989Ala)
n.3015C>G
c.3217C>G (p.Pro1073Ala)
c.3118C>G (p.Pro1040Ala)
c.3532C>G (p.Pro1178Ala)
 dbSNP gnomAD v4
16g.9764168G=CA2206693084GRIN2Ac.3376C= (p.Pro1126=)
c.2905C= (p.Pro969=)
n.2969C=
c.*746C= (n.*746C=)
c.2965C= (p.Pro989=)
n.3015C=
c.3217C= (p.Pro1073=)
c.3118C= (p.Pro1040=)
c.3532C= (p.Pro1178=)
16g.9764168G>TCA7896327GRIN2Ac.3376C>A (p.Pro1126Thr)
c.2905C>A (p.Pro969Thr)
n.2969C>A
c.*746C>A (n.*746C>A)
c.2965C>A (p.Pro989Thr)
n.3015C>A
c.3217C>A (p.Pro1073Thr)
c.3118C>A (p.Pro1040Thr)
c.3532C>A (p.Pro1178Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.9764169C>ACA394708004GRIN2Ac.3375G>T (p.Glu1125Asp)
c.2904G>T (p.Glu968Asp)
n.2968G>T
c.*745G>T (n.*745G>T)
c.2964G>T (p.Glu988Asp)
n.3014G>T
c.3216G>T (p.Glu1072Asp)
c.3117G>T (p.Glu1039Asp)
c.3531G>T (p.Glu1177Asp)
 dbSNP
16g.9764169C=CA2206693085GRIN2Ac.3375G= (p.Glu1125=)
c.2904G= (p.Glu968=)
n.2968G=
c.*745G= (n.*745G=)
c.2964G= (p.Glu988=)
n.3014G=
c.3216G= (p.Glu1072=)
c.3117G= (p.Glu1039=)
c.3531G= (p.Glu1177=)
16g.9764169C>GCA394708005GRIN2Ac.3375G>C (p.Glu1125Asp)
c.2904G>C (p.Glu968Asp)
n.2968G>C
c.*745G>C (n.*745G>C)
c.2964G>C (p.Glu988Asp)
n.3014G>C
c.3216G>C (p.Glu1072Asp)
c.3117G>C (p.Glu1039Asp)
c.3531G>C (p.Glu1177Asp)
 ClinVar dbSNP gnomAD v4
16g.9764169C>TCA493692948GRIN2Ac.3375G>A (p.Glu1125=)
c.2904G>A (p.Glu968=)
n.2968G>A
c.*745G>A (n.*745G>A)
c.2964G>A (p.Glu988=)
n.3014G>A
c.3216G>A (p.Glu1072=)
c.3117G>A (p.Glu1039=)
c.3531G>A (p.Glu1177=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
16g.9764170T>ACA394708006GRIN2Ac.3374A>T (p.Glu1125Val)
c.2903A>T (p.Glu968Val)
n.2967A>T
c.*744A>T (n.*744A>T)
c.2963A>T (p.Glu988Val)
n.3013A>T
c.3215A>T (p.Glu1072Val)
c.3116A>T (p.Glu1039Val)
c.3530A>T (p.Glu1177Val)
 dbSNP
16g.9764170T>CCA394708008GRIN2Ac.3374A>G (p.Glu1125Gly)
c.2903A>G (p.Glu968Gly)
n.2967A>G
c.*744A>G (n.*744A>G)
c.2963A>G (p.Glu988Gly)
n.3013A>G
c.3215A>G (p.Glu1072Gly)
c.3116A>G (p.Glu1039Gly)
c.3530A>G (p.Glu1177Gly)
16g.9764170T>GCA394708009GRIN2Ac.3374A>C (p.Glu1125Ala)
c.2903A>C (p.Glu968Ala)
n.2967A>C
c.*744A>C (n.*744A>C)
c.2963A>C (p.Glu988Ala)
n.3013A>C
c.3215A>C (p.Glu1072Ala)
c.3116A>C (p.Glu1039Ala)
c.3530A>C (p.Glu1177Ala)
16g.9764171C>ACA394708010GRIN2Ac.3373G>T (p.Glu1125Ter)
c.2902G>T (p.Glu968Ter)
n.2966G>T
c.*743G>T (n.*743G>T)
c.2962G>T (p.Glu988Ter)
n.3012G>T
c.3214G>T (p.Glu1072Ter)
c.3115G>T (p.Glu1039Ter)
c.3529G>T (p.Glu1177Ter)
 dbSNP COSMIC
16g.9764171C=CA2206693086GRIN2Ac.3373G= (p.Glu1125=)
c.2902G= (p.Glu968=)
n.2966G=
c.*743G= (n.*743G=)
c.2962G= (p.Glu988=)
n.3012G=
c.3214G= (p.Glu1072=)
c.3115G= (p.Glu1039=)
c.3529G= (p.Glu1177=)
16g.9764171C>GCA394708011GRIN2Ac.3373G>C (p.Glu1125Gln)
c.2902G>C (p.Glu968Gln)
n.2966G>C
c.*743G>C (n.*743G>C)
c.2962G>C (p.Glu988Gln)
n.3012G>C
c.3214G>C (p.Glu1072Gln)
c.3115G>C (p.Glu1039Gln)
c.3529G>C (p.Glu1177Gln)
 dbSNP
16g.9764171C>TCA394708012GRIN2Ac.3373G>A (p.Glu1125Lys)
c.2902G>A (p.Glu968Lys)
n.2966G>A
c.*743G>A (n.*743G>A)
c.2962G>A (p.Glu988Lys)
n.3012G>A
c.3214G>A (p.Glu1072Lys)
c.3115G>A (p.Glu1039Lys)
c.3529G>A (p.Glu1177Lys)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.9764172C>ACA394708013GRIN2Ac.3372G>T (p.Lys1124Asn)
c.2901G>T (p.Lys967Asn)
n.2965G>T
c.*742G>T (n.*742G>T)
c.2961G>T (p.Lys987Asn)
n.3011G>T
c.3213G>T (p.Lys1071Asn)
c.3114G>T (p.Lys1038Asn)
c.3528G>T (p.Lys1176Asn)
 dbSNP COSMIC
16g.9764172C=CA2206693087GRIN2Ac.3372G= (p.Lys1124=)
c.2901G= (p.Lys967=)
n.2965G=
c.*742G= (n.*742G=)
c.2961G= (p.Lys987=)
n.3011G=
c.3213G= (p.Lys1071=)
c.3114G= (p.Lys1038=)
c.3528G= (p.Lys1176=)
16g.9764172C>GCA394708014GRIN2Ac.3372G>C (p.Lys1124Asn)
c.2901G>C (p.Lys967Asn)
n.2965G>C
c.*742G>C (n.*742G>C)
c.2961G>C (p.Lys987Asn)
n.3011G>C
c.3213G>C (p.Lys1071Asn)
c.3114G>C (p.Lys1038Asn)
c.3528G>C (p.Lys1176Asn)
16g.9764172C>TCA277537344GRIN2Ac.3372G>A (p.Lys1124=)
c.2901G>A (p.Lys967=)
n.2965G>A
c.*742G>A (n.*742G>A)
c.2961G>A (p.Lys987=)
n.3011G>A
c.3213G>A (p.Lys1071=)
c.3114G>A (p.Lys1038=)
c.3528G>A (p.Lys1176=)
 dbSNP COSMIC
16g.9764173T>ACA394708016GRIN2Ac.3371A>T (p.Lys1124Met)
c.2900A>T (p.Lys967Met)
n.2964A>T
c.*741A>T (n.*741A>T)
c.2960A>T (p.Lys987Met)
n.3010A>T
c.3212A>T (p.Lys1071Met)
c.3113A>T (p.Lys1038Met)
c.3527A>T (p.Lys1176Met)
 dbSNP
16g.9764173T>CCA394708017GRIN2Ac.3371A>G (p.Lys1124Arg)
c.2900A>G (p.Lys967Arg)
n.2964A>G
c.*741A>G (n.*741A>G)
c.2960A>G (p.Lys987Arg)
n.3010A>G
c.3212A>G (p.Lys1071Arg)
c.3113A>G (p.Lys1038Arg)
c.3527A>G (p.Lys1176Arg)
 dbSNP
16g.9764173T>GCA394708015GRIN2Ac.3371A>C (p.Lys1124Thr)
c.2900A>C (p.Lys967Thr)
n.2964A>C
c.*741A>C (n.*741A>C)
c.2960A>C (p.Lys987Thr)
n.3010A>C
c.3212A>C (p.Lys1071Thr)
c.3113A>C (p.Lys1038Thr)
c.3527A>C (p.Lys1176Thr)
 dbSNP gnomAD v3 gnomAD v4
16g.9764173T=CA2206693088GRIN2Ac.3371A= (p.Lys1124=)
c.2900A= (p.Lys967=)
n.2964A=
c.*741A= (n.*741A=)
c.2960A= (p.Lys987=)
n.3010A=
c.3212A= (p.Lys1071=)
c.3113A= (p.Lys1038=)
c.3527A= (p.Lys1176=)
16g.9764174T>ACA394708018GRIN2Ac.3370A>T (p.Lys1124Ter)
c.2899A>T (p.Lys967Ter)
n.2963A>T
c.*740A>T (n.*740A>T)
c.2959A>T (p.Lys987Ter)
n.3009A>T
c.3211A>T (p.Lys1071Ter)
c.3112A>T (p.Lys1038Ter)
c.3526A>T (p.Lys1176Ter)
 dbSNP
16g.9764174T>CCA394708019GRIN2Ac.3370A>G (p.Lys1124Glu)
c.2899A>G (p.Lys967Glu)
n.2963A>G
c.*740A>G (n.*740A>G)
c.2959A>G (p.Lys987Glu)
n.3009A>G
c.3211A>G (p.Lys1071Glu)
c.3112A>G (p.Lys1038Glu)
c.3526A>G (p.Lys1176Glu)
16g.9764174T>GCA394708020GRIN2Ac.3370A>C (p.Lys1124Gln)
c.2899A>C (p.Lys967Gln)
n.2963A>C
c.*740A>C (n.*740A>C)
c.2959A>C (p.Lys987Gln)
n.3009A>C
c.3211A>C (p.Lys1071Gln)
c.3112A>C (p.Lys1038Gln)
c.3526A>C (p.Lys1176Gln)
16g.9764174T=CA2206693089GRIN2Ac.3370A= (p.Lys1124=)
c.2899A= (p.Lys967=)
n.2963A=
c.*740A= (n.*740A=)
c.2959A= (p.Lys987=)
n.3009A=
c.3211A= (p.Lys1071=)
c.3112A= (p.Lys1038=)
c.3526A= (p.Lys1176=)
16g.9764175C>ACA394708021GRIN2Ac.3369G>T (p.Glu1123Asp)
c.2898G>T (p.Glu966Asp)
n.2962G>T
c.*739G>T (n.*739G>T)
c.2958G>T (p.Glu986Asp)
n.3008G>T
c.3210G>T (p.Glu1070Asp)
c.3111G>T (p.Glu1037Asp)
c.3525G>T (p.Glu1175Asp)
 dbSNP
16g.9764175C>GCA394708022GRIN2Ac.3369G>C (p.Glu1123Asp)
c.2898G>C (p.Glu966Asp)
n.2962G>C
c.*739G>C (n.*739G>C)
c.2958G>C (p.Glu986Asp)
n.3008G>C
c.3210G>C (p.Glu1070Asp)
c.3111G>C (p.Glu1037Asp)
c.3525G>C (p.Glu1175Asp)
 dbSNP gnomAD v4
16g.9764175C>TCA493692959GRIN2Ac.3369G>A (p.Glu1123=)
c.2898G>A (p.Glu966=)
n.2962G>A
c.*739G>A (n.*739G>A)
c.2958G>A (p.Glu986=)
n.3008G>A
c.3210G>A (p.Glu1070=)
c.3111G>A (p.Glu1037=)
c.3525G>A (p.Glu1175=)
 gnomAD v4
16g.9764176T>ACA394708025GRIN2Ac.3368A>T (p.Glu1123Val)
c.2897A>T (p.Glu966Val)
n.2961A>T
c.*738A>T (n.*738A>T)
c.2957A>T (p.Glu986Val)
n.3007A>T
c.3209A>T (p.Glu1070Val)
c.3110A>T (p.Glu1037Val)
c.3524A>T (p.Glu1175Val)
 dbSNP
16g.9764176T>CCA394708023GRIN2Ac.3368A>G (p.Glu1123Gly)
c.2897A>G (p.Glu966Gly)
n.2961A>G
c.*738A>G (n.*738A>G)
c.2957A>G (p.Glu986Gly)
n.3007A>G
c.3209A>G (p.Glu1070Gly)
c.3110A>G (p.Glu1037Gly)
c.3524A>G (p.Glu1175Gly)
 dbSNP
16g.9764176T>GCA394708024GRIN2Ac.3368A>C (p.Glu1123Ala)
c.2897A>C (p.Glu966Ala)
n.2961A>C
c.*738A>C (n.*738A>C)
c.2957A>C (p.Glu986Ala)
n.3007A>C
c.3209A>C (p.Glu1070Ala)
c.3110A>C (p.Glu1037Ala)
c.3524A>C (p.Glu1175Ala)
 dbSNP gnomAD v2 gnomAD v4
16g.9764176T=CA2206693090GRIN2Ac.3368A= (p.Glu1123=)
c.2897A= (p.Glu966=)
n.2961A=
c.*738A= (n.*738A=)
c.2957A= (p.Glu986=)
n.3007A=
c.3209A= (p.Glu1070=)
c.3110A= (p.Glu1037=)
c.3524A= (p.Glu1175=)
16g.9764177C>ACA394708026GRIN2Ac.3367G>T (p.Glu1123Ter)
c.2896G>T (p.Glu966Ter)
n.2960G>T
c.*737G>T (n.*737G>T)
c.2956G>T (p.Glu986Ter)
n.3006G>T
c.3208G>T (p.Glu1070Ter)
c.3109G>T (p.Glu1037Ter)
c.3523G>T (p.Glu1175Ter)
 dbSNP COSMIC
16g.9764177C=CA2206693091GRIN2Ac.3367G= (p.Glu1123=)
c.2896G= (p.Glu966=)
n.2960G=
c.*737G= (n.*737G=)
c.2956G= (p.Glu986=)
n.3006G=
c.3208G= (p.Glu1070=)
c.3109G= (p.Glu1037=)
c.3523G= (p.Glu1175=)
16g.9764177C>GCA394708027GRIN2Ac.3367G>C (p.Glu1123Gln)
c.2896G>C (p.Glu966Gln)
n.2960G>C
c.*737G>C (n.*737G>C)
c.2956G>C (p.Glu986Gln)
n.3006G>C
c.3208G>C (p.Glu1070Gln)
c.3109G>C (p.Glu1037Gln)
c.3523G>C (p.Glu1175Gln)
 dbSNP
16g.9764177C>TCA7896328GRIN2Ac.3367G>A (p.Glu1123Lys)
c.2896G>A (p.Glu966Lys)
n.2960G>A
c.*737G>A (n.*737G>A)
c.2956G>A (p.Glu986Lys)
n.3006G>A
c.3208G>A (p.Glu1070Lys)
c.3109G>A (p.Glu1037Lys)
c.3523G>A (p.Glu1175Lys)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.9764178A=CA2206693092GRIN2Ac.3366T= (p.Gly1122=)
c.2895T= (p.Gly965=)
n.2959T=
c.*736T= (n.*736T=)
c.2955T= (p.Gly985=)
n.3005T=
c.3207T= (p.Gly1069=)
c.3108T= (p.Gly1036=)
c.3522T= (p.Gly1174=)
16g.9764178A>CCA16615064GRIN2Ac.3366T>G (p.Gly1122=)
c.2895T>G (p.Gly965=)
n.2959T>G
c.*736T>G (n.*736T>G)
c.2955T>G (p.Gly985=)
n.3005T>G
c.3207T>G (p.Gly1069=)
c.3108T>G (p.Gly1036=)
c.3522T>G (p.Gly1174=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
16g.9764178A>GCA493692962GRIN2Ac.3366T>C (p.Gly1122=)
c.2895T>C (p.Gly965=)
n.2959T>C
c.*736T>C (n.*736T>C)
c.2955T>C (p.Gly985=)
n.3005T>C
c.3207T>C (p.Gly1069=)
c.3108T>C (p.Gly1036=)
c.3522T>C (p.Gly1174=)
16g.9764178A>TCA493692963GRIN2Ac.3366T>A (p.Gly1122=)
c.2895T>A (p.Gly965=)
n.2959T>A
c.*736T>A (n.*736T>A)
c.2955T>A (p.Gly985=)
n.3005T>A
c.3207T>A (p.Gly1069=)
c.3108T>A (p.Gly1036=)
c.3522T>A (p.Gly1174=)
16g.9764179C>ACA7896329GRIN2Ac.3365G>T (p.Gly1122Val)
c.2894G>T (p.Gly965Val)
n.2958G>T
c.*735G>T (n.*735G>T)
c.2954G>T (p.Gly985Val)
n.3004G>T
c.3206G>T (p.Gly1069Val)
c.3107G>T (p.Gly1036Val)
c.3521G>T (p.Gly1174Val)
 dbSNP ExAC gnomAD v2
16g.9764179C=CA2206693093GRIN2Ac.3365G= (p.Gly1122=)
c.2894G= (p.Gly965=)
n.2958G=
c.*735G= (n.*735G=)
c.2954G= (p.Gly985=)
n.3004G=
c.3206G= (p.Gly1069=)
c.3107G= (p.Gly1036=)
c.3521G= (p.Gly1174=)
16g.9764179C>GCA394708028GRIN2Ac.3365G>C (p.Gly1122Ala)
c.2894G>C (p.Gly965Ala)
n.2958G>C
c.*735G>C (n.*735G>C)
c.2954G>C (p.Gly985Ala)
n.3004G>C
c.3206G>C (p.Gly1069Ala)
c.3107G>C (p.Gly1036Ala)
c.3521G>C (p.Gly1174Ala)
 ClinVar dbSNP gnomAD v4
16g.9764179C>TCA314978GRIN2Ac.3365G>A (p.Gly1122Asp)
c.2894G>A (p.Gly965Asp)
n.2958G>A
c.*735G>A (n.*735G>A)
c.2954G>A (p.Gly985Asp)
n.3004G>A
c.3206G>A (p.Gly1069Asp)
c.3107G>A (p.Gly1036Asp)
c.3521G>A (p.Gly1174Asp)
 ClinVar dbSNP
16g.9764180C>ACA394708030GRIN2Ac.3364G>T (p.Gly1122Cys)
c.2893G>T (p.Gly965Cys)
n.2957G>T
c.*734G>T (n.*734G>T)
c.2953G>T (p.Gly985Cys)
n.3003G>T
c.3205G>T (p.Gly1069Cys)
c.3106G>T (p.Gly1036Cys)
c.3520G>T (p.Gly1174Cys)
 dbSNP
16g.9764180C>GCA394708031GRIN2Ac.3364G>C (p.Gly1122Arg)
c.2893G>C (p.Gly965Arg)
n.2957G>C
c.*734G>C (n.*734G>C)
c.2953G>C (p.Gly985Arg)
n.3003G>C
c.3205G>C (p.Gly1069Arg)
c.3106G>C (p.Gly1036Arg)
c.3520G>C (p.Gly1174Arg)
 dbSNP
16g.9764180C>TCA394708029GRIN2Ac.3364G>A (p.Gly1122Ser)
c.2893G>A (p.Gly965Ser)
n.2957G>A
c.*734G>A (n.*734G>A)
c.2953G>A (p.Gly985Ser)
n.3003G>A
c.3205G>A (p.Gly1069Ser)
c.3106G>A (p.Gly1036Ser)
c.3520G>A (p.Gly1174Ser)
16g.9764181A=CA2206693094GRIN2Ac.3363T= (p.Asp1121=)
c.2892T= (p.Asp964=)
n.2956T=
c.*733T= (n.*733T=)
c.2952T= (p.Asp984=)
n.3002T=
c.3204T= (p.Asp1068=)
c.3105T= (p.Asp1035=)
c.3519T= (p.Asp1173=)
16g.9764181A>CCA314976GRIN2Ac.3363T>G (p.Asp1121Glu)
c.2892T>G (p.Asp964Glu)
n.2956T>G
c.*733T>G (n.*733T>G)
c.2952T>G (p.Asp984Glu)
n.3002T>G
c.3204T>G (p.Asp1068Glu)
c.3105T>G (p.Asp1035Glu)
c.3519T>G (p.Asp1173Glu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.9764181A>GCA493692968GRIN2Ac.3363T>C (p.Asp1121=)
c.2892T>C (p.Asp964=)
n.2956T>C
c.*733T>C (n.*733T>C)
c.2952T>C (p.Asp984=)
n.3002T>C
c.3204T>C (p.Asp1068=)
c.3105T>C (p.Asp1035=)
c.3519T>C (p.Asp1173=)
 ClinVar
16g.9764181A>TCA394708032GRIN2Ac.3363T>A (p.Asp1121Glu)
c.2892T>A (p.Asp964Glu)
n.2956T>A
c.*733T>A (n.*733T>A)
c.2952T>A (p.Asp984Glu)
n.3002T>A
c.3204T>A (p.Asp1068Glu)
c.3105T>A (p.Asp1035Glu)
c.3519T>A (p.Asp1173Glu)
 dbSNP
16g.9764182T>ACA394708033GRIN2Ac.3362A>T (p.Asp1121Val)
c.2891A>T (p.Asp964Val)
n.2955A>T
c.*732A>T (n.*732A>T)
c.2951A>T (p.Asp984Val)
n.3001A>T
c.3203A>T (p.Asp1068Val)
c.3104A>T (p.Asp1035Val)
c.3518A>T (p.Asp1173Val)
 dbSNP
16g.9764182T>CCA7896330GRIN2Ac.3362A>G (p.Asp1121Gly)
c.2891A>G (p.Asp964Gly)
n.2955A>G
c.*732A>G (n.*732A>G)
c.2951A>G (p.Asp984Gly)
n.3001A>G
c.3203A>G (p.Asp1068Gly)
c.3104A>G (p.Asp1035Gly)
c.3518A>G (p.Asp1173Gly)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
16g.9764182T>GCA394708034GRIN2Ac.3362A>C (p.Asp1121Ala)
c.2891A>C (p.Asp964Ala)
n.2955A>C
c.*732A>C (n.*732A>C)
c.2951A>C (p.Asp984Ala)
n.3001A>C
c.3203A>C (p.Asp1068Ala)
c.3104A>C (p.Asp1035Ala)
c.3518A>C (p.Asp1173Ala)
 gnomAD v3 gnomAD v4
16g.9764182T=CA2206693095GRIN2Ac.3362A= (p.Asp1121=)
c.2891A= (p.Asp964=)
n.2955A=
c.*732A= (n.*732A=)
c.2951A= (p.Asp984=)
n.3001A=
c.3203A= (p.Asp1068=)
c.3104A= (p.Asp1035=)
c.3518A= (p.Asp1173=)
16g.9764183C>ACA7896331GRIN2Ac.3361G>T (p.Asp1121Tyr)
c.2890G>T (p.Asp964Tyr)
n.2954G>T
c.*731G>T (n.*731G>T)
c.2950G>T (p.Asp984Tyr)
n.3000G>T
c.3202G>T (p.Asp1068Tyr)
c.3103G>T (p.Asp1035Tyr)
c.3517G>T (p.Asp1173Tyr)
 dbSNP ExAC gnomAD v2
16g.9764183C=CA2206693096GRIN2Ac.3361G= (p.Asp1121=)
c.2890G= (p.Asp964=)
n.2954G=
c.*731G= (n.*731G=)
c.2950G= (p.Asp984=)
n.3000G=
c.3202G= (p.Asp1068=)
c.3103G= (p.Asp1035=)
c.3517G= (p.Asp1173=)
16g.9764183C>GCA394708035GRIN2Ac.3361G>C (p.Asp1121His)
c.2890G>C (p.Asp964His)
n.2954G>C
c.*731G>C (n.*731G>C)
c.2950G>C (p.Asp984His)
n.3000G>C
c.3202G>C (p.Asp1068His)
c.3103G>C (p.Asp1035His)
c.3517G>C (p.Asp1173His)
 dbSNP gnomAD v3 gnomAD v4 COSMIC
16g.9764183C>TCA394708036GRIN2Ac.3361G>A (p.Asp1121Asn)
c.2890G>A (p.Asp964Asn)
n.2954G>A
c.*731G>A (n.*731G>A)
c.2950G>A (p.Asp984Asn)
n.3000G>A
c.3202G>A (p.Asp1068Asn)
c.3103G>A (p.Asp1035Asn)
c.3517G>A (p.Asp1173Asn)
 dbSNP COSMIC
16g.9764184T>ACA493692972GRIN2Ac.3360A>T (p.Ile1120=)
c.2889A>T (p.Ile963=)
n.2953A>T
c.*730A>T (n.*730A>T)
c.2949A>T (p.Ile983=)
n.2999A>T
c.3201A>T (p.Ile1067=)
c.3102A>T (p.Ile1034=)
c.3516A>T (p.Ile1172=)
 dbSNP gnomAD v3 gnomAD v4
16g.9764184T>CCA394708037GRIN2Ac.3360A>G (p.Ile1120Met)
c.2889A>G (p.Ile963Met)
n.2953A>G
c.*730A>G (n.*730A>G)
c.2949A>G (p.Ile983Met)
n.2999A>G
c.3201A>G (p.Ile1067Met)
c.3102A>G (p.Ile1034Met)
c.3516A>G (p.Ile1172Met)
16g.9764184T>GCA493692973GRIN2Ac.3360A>C (p.Ile1120=)
c.2889A>C (p.Ile963=)
n.2953A>C
c.*730A>C (n.*730A>C)
c.2949A>C (p.Ile983=)
n.2999A>C
c.3201A>C (p.Ile1067=)
c.3102A>C (p.Ile1034=)
c.3516A>C (p.Ile1172=)
16g.9764185A>CCA394708038GRIN2Ac.3359T>G (p.Ile1120Arg)
c.2888T>G (p.Ile963Arg)
n.2952T>G
c.*729T>G (n.*729T>G)
c.2948T>G (p.Ile983Arg)
n.2998T>G
c.3200T>G (p.Ile1067Arg)
c.3101T>G (p.Ile1034Arg)
c.3515T>G (p.Ile1172Arg)
 ClinVar dbSNP
16g.9764185A>GCA394708039GRIN2Ac.3359T>C (p.Ile1120Thr)
c.2888T>C (p.Ile963Thr)
n.2952T>C
c.*729T>C (n.*729T>C)
c.2948T>C (p.Ile983Thr)
n.2998T>C
c.3200T>C (p.Ile1067Thr)
c.3101T>C (p.Ile1034Thr)
c.3515T>C (p.Ile1172Thr)
16g.9764185A>TCA394708040GRIN2Ac.3359T>A (p.Ile1120Lys)
c.2888T>A (p.Ile963Lys)
n.2952T>A
c.*729T>A (n.*729T>A)
c.2948T>A (p.Ile983Lys)
n.2998T>A
c.3200T>A (p.Ile1067Lys)
c.3101T>A (p.Ile1034Lys)
c.3515T>A (p.Ile1172Lys)
 dbSNP
16g.9764185_9764186insCACCCA2573152117GRIN2Ac.3358_3359insGGTG (p.Ile1120ArgfsTer5)
c.2887_2888insGGTG (p.Ile963ArgfsTer5)
n.2951_2952insGGTG
c.*728_*729insGGTG (n.*728_*729insGGTG)
c.2947_2948insGGTG (p.Ile983ArgfsTer5)
n.2997_2998insGGTG
c.3199_3200insGGTG (p.Ile1067ArgfsTer5)
c.3100_3101insGGTG (p.Ile1034ArgfsTer5)
c.3514_3515insGGTG (p.Ile1172ArgfsTer5)
 dbSNP gnomAD v4
16g.9764186T>ACA394708041GRIN2Ac.3358A>T (p.Ile1120Leu)
c.2887A>T (p.Ile963Leu)
n.2951A>T
c.*728A>T (n.*728A>T)
c.2947A>T (p.Ile983Leu)
n.2997A>T
c.3199A>T (p.Ile1067Leu)
c.3100A>T (p.Ile1034Leu)
c.3514A>T (p.Ile1172Leu)
 dbSNP gnomAD v4
16g.9764186T>CCA394708042GRIN2Ac.3358A>G (p.Ile1120Val)
c.2887A>G (p.Ile963Val)
n.2951A>G
c.*728A>G (n.*728A>G)
c.2947A>G (p.Ile983Val)
n.2997A>G
c.3199A>G (p.Ile1067Val)
c.3100A>G (p.Ile1034Val)
c.3514A>G (p.Ile1172Val)
 dbSNP gnomAD v4
16g.9764186T>GCA394708043GRIN2Ac.3358A>C (p.Ile1120Leu)
c.2887A>C (p.Ile963Leu)
n.2951A>C
c.*728A>C (n.*728A>C)
c.2947A>C (p.Ile983Leu)
n.2997A>C
c.3199A>C (p.Ile1067Leu)
c.3100A>C (p.Ile1034Leu)
c.3514A>C (p.Ile1172Leu)
16g.9764187A=CA2206693097GRIN2Ac.3357T= (p.Thr1119=)
c.2886T= (p.Thr962=)
n.2950T=
c.*727T= (n.*727T=)
c.2946T= (p.Thr982=)
n.2996T=
c.3198T= (p.Thr1066=)
c.3099T= (p.Thr1033=)
c.3513T= (p.Thr1171=)
16g.9764187A>CCA493692974GRIN2Ac.3357T>G (p.Thr1119=)
c.2886T>G (p.Thr962=)
n.2950T>G
c.*727T>G (n.*727T>G)
c.2946T>G (p.Thr982=)
n.2996T>G
c.3198T>G (p.Thr1066=)
c.3099T>G (p.Thr1033=)
c.3513T>G (p.Thr1171=)
16g.9764187A>GCA493692975GRIN2Ac.3357T>C (p.Thr1119=)
c.2886T>C (p.Thr962=)
n.2950T>C
c.*727T>C (n.*727T>C)
c.2946T>C (p.Thr982=)
n.2996T>C
c.3198T>C (p.Thr1066=)
c.3099T>C (p.Thr1033=)
c.3513T>C (p.Thr1171=)
 ClinVar dbSNP
16g.9764187A>TCA493692976GRIN2Ac.3357T>A (p.Thr1119=)
c.2886T>A (p.Thr962=)
n.2950T>A
c.*727T>A (n.*727T>A)
c.2946T>A (p.Thr982=)
n.2996T>A
c.3198T>A (p.Thr1066=)
c.3099T>A (p.Thr1033=)
c.3513T>A (p.Thr1171=)
 dbSNP
16g.9764188G>ACA394708044GRIN2Ac.3356C>T (p.Thr1119Ile)
c.2885C>T (p.Thr962Ile)
n.2949C>T
c.*726C>T (n.*726C>T)
c.2945C>T (p.Thr982Ile)
n.2995C>T
c.3197C>T (p.Thr1066Ile)
c.3098C>T (p.Thr1033Ile)
c.3512C>T (p.Thr1171Ile)
 dbSNP gnomAD v4
16g.9764188G>CCA394708046GRIN2Ac.3356C>G (p.Thr1119Ser)
c.2885C>G (p.Thr962Ser)
n.2949C>G
c.*726C>G (n.*726C>G)
c.2945C>G (p.Thr982Ser)
n.2995C>G
c.3197C>G (p.Thr1066Ser)
c.3098C>G (p.Thr1033Ser)
c.3512C>G (p.Thr1171Ser)
 dbSNP
16g.9764188G>TCA394708045GRIN2Ac.3356C>A (p.Thr1119Asn)
c.2885C>A (p.Thr962Asn)
n.2949C>A
c.*726C>A (n.*726C>A)
c.2945C>A (p.Thr982Asn)
n.2995C>A
c.3197C>A (p.Thr1066Asn)
c.3098C>A (p.Thr1033Asn)
c.3512C>A (p.Thr1171Asn)
 COSMIC
16g.9764189T>ACA394708047GRIN2Ac.3355A>T (p.Thr1119Ser)
c.2884A>T (p.Thr962Ser)
n.2948A>T
c.*725A>T (n.*725A>T)
c.2944A>T (p.Thr982Ser)
n.2994A>T
c.3196A>T (p.Thr1066Ser)
c.3097A>T (p.Thr1033Ser)
c.3511A>T (p.Thr1171Ser)
 dbSNP gnomAD v4
16g.9764189T>CCA394708048GRIN2Ac.3355A>G (p.Thr1119Ala)
c.2884A>G (p.Thr962Ala)
n.2948A>G
c.*725A>G (n.*725A>G)
c.2944A>G (p.Thr982Ala)
n.2994A>G
c.3196A>G (p.Thr1066Ala)
c.3097A>G (p.Thr1033Ala)
c.3511A>G (p.Thr1171Ala)
16g.9764189T>GCA394708049GRIN2Ac.3355A>C (p.Thr1119Pro)
c.2884A>C (p.Thr962Pro)
n.2948A>C
c.*725A>C (n.*725A>C)
c.2944A>C (p.Thr982Pro)
n.2994A>C
c.3196A>C (p.Thr1066Pro)
c.3097A>C (p.Thr1033Pro)
c.3511A>C (p.Thr1171Pro)
 COSMIC
16g.9764190G>ACA493692978GRIN2Ac.3354C>T (p.Tyr1118=)
c.2883C>T (p.Tyr961=)
n.2947C>T
c.*724C>T (n.*724C>T)
c.2943C>T (p.Tyr981=)
n.2993C>T
c.3195C>T (p.Tyr1065=)
c.3096C>T (p.Tyr1032=)
c.3510C>T (p.Tyr1170=)
 dbSNP
16g.9764190G>CCA394708050GRIN2Ac.3354C>G (p.Tyr1118Ter)
c.2883C>G (p.Tyr961Ter)
n.2947C>G
c.*724C>G (n.*724C>G)
c.2943C>G (p.Tyr981Ter)
n.2993C>G
c.3195C>G (p.Tyr1065Ter)
c.3096C>G (p.Tyr1032Ter)
c.3510C>G (p.Tyr1170Ter)
 dbSNP
16g.9764190G>TCA394708051GRIN2Ac.3354C>A (p.Tyr1118Ter)
c.2883C>A (p.Tyr961Ter)
n.2947C>A
c.*724C>A (n.*724C>A)
c.2943C>A (p.Tyr981Ter)
n.2993C>A
c.3195C>A (p.Tyr1065Ter)
c.3096C>A (p.Tyr1032Ter)
c.3510C>A (p.Tyr1170Ter)
16g.9764191T>ACA394708052GRIN2Ac.3353A>T (p.Tyr1118Phe)
c.2882A>T (p.Tyr961Phe)
n.2946A>T
c.*723A>T (n.*723A>T)
c.2942A>T (p.Tyr981Phe)
n.2992A>T
c.3194A>T (p.Tyr1065Phe)
c.3095A>T (p.Tyr1032Phe)
c.3509A>T (p.Tyr1170Phe)
 dbSNP
16g.9764191T>CCA394708053GRIN2Ac.3353A>G (p.Tyr1118Cys)
c.2882A>G (p.Tyr961Cys)
n.2946A>G
c.*723A>G (n.*723A>G)
c.2942A>G (p.Tyr981Cys)
n.2992A>G
c.3194A>G (p.Tyr1065Cys)
c.3095A>G (p.Tyr1032Cys)
c.3509A>G (p.Tyr1170Cys)
16g.9764191T>GCA394708054GRIN2Ac.3353A>C (p.Tyr1118Ser)
c.2882A>C (p.Tyr961Ser)
n.2946A>C
c.*723A>C (n.*723A>C)
c.2942A>C (p.Tyr981Ser)
n.2992A>C
c.3194A>C (p.Tyr1065Ser)
c.3095A>C (p.Tyr1032Ser)
c.3509A>C (p.Tyr1170Ser)
16g.9764192A>CCA394708055GRIN2Ac.3352T>G (p.Tyr1118Asp)
c.2881T>G (p.Tyr961Asp)
n.2945T>G
c.*722T>G (n.*722T>G)
c.2941T>G (p.Tyr981Asp)
n.2991T>G
c.3193T>G (p.Tyr1065Asp)
c.3094T>G (p.Tyr1032Asp)
c.3508T>G (p.Tyr1170Asp)
16g.9764192A>GCA394708056GRIN2Ac.3352T>C (p.Tyr1118His)
c.2881T>C (p.Tyr961His)
n.2945T>C
c.*722T>C (n.*722T>C)
c.2941T>C (p.Tyr981His)
n.2991T>C
c.3193T>C (p.Tyr1065His)
c.3094T>C (p.Tyr1032His)
c.3508T>C (p.Tyr1170His)
16g.9764192A>TCA394708057GRIN2Ac.3352T>A (p.Tyr1118Asn)
c.2881T>A (p.Tyr961Asn)
n.2945T>A
c.*722T>A (n.*722T>A)
c.2941T>A (p.Tyr981Asn)
n.2991T>A
c.3193T>A (p.Tyr1065Asn)
c.3094T>A (p.Tyr1032Asn)
c.3508T>A (p.Tyr1170Asn)
 dbSNP
16g.9764193G>ACA493692981GRIN2Ac.3351C>T (p.Ile1117=)
c.2880C>T (p.Ile960=)
n.2944C>T
c.*721C>T (n.*721C>T)
c.2940C>T (p.Ile980=)
n.2990C>T
c.3192C>T (p.Ile1064=)
c.3093C>T (p.Ile1031=)
c.3507C>T (p.Ile1169=)
 dbSNP gnomAD v4
16g.9764193G>CCA394708058GRIN2Ac.3351C>G (p.Ile1117Met)
c.2880C>G (p.Ile960Met)
n.2944C>G
c.*721C>G (n.*721C>G)
c.2940C>G (p.Ile980Met)
n.2990C>G
c.3192C>G (p.Ile1064Met)
c.3093C>G (p.Ile1031Met)
c.3507C>G (p.Ile1169Met)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.9764193G=CA2206693098GRIN2Ac.3351C= (p.Ile1117=)
c.2880C= (p.Ile960=)
n.2944C=
c.*721C= (n.*721C=)
c.2940C= (p.Ile980=)
n.2990C=
c.3192C= (p.Ile1064=)
c.3093C= (p.Ile1031=)
c.3507C= (p.Ile1169=)
16g.9764193G>TCA493692980GRIN2Ac.3351C>A (p.Ile1117=)
c.2880C>A (p.Ile960=)
n.2944C>A
c.*721C>A (n.*721C>A)
c.2940C>A (p.Ile980=)
n.2990C>A
c.3192C>A (p.Ile1064=)
c.3093C>A (p.Ile1031=)
c.3507C>A (p.Ile1169=)
 dbSNP
16g.9764194A>CCA394708059GRIN2Ac.3350T>G (p.Ile1117Ser)
c.2879T>G (p.Ile960Ser)
n.2943T>G
c.*720T>G (n.*720T>G)
c.2939T>G (p.Ile980Ser)
n.2989T>G
c.3191T>G (p.Ile1064Ser)
c.3092T>G (p.Ile1031Ser)
c.3506T>G (p.Ile1169Ser)
 dbSNP
16g.9764194A>GCA394708061GRIN2Ac.3350T>C (p.Ile1117Thr)
c.2879T>C (p.Ile960Thr)
n.2943T>C
c.*720T>C (n.*720T>C)
c.2939T>C (p.Ile980Thr)
n.2989T>C
c.3191T>C (p.Ile1064Thr)
c.3092T>C (p.Ile1031Thr)
c.3506T>C (p.Ile1169Thr)
16g.9764194A>TCA394708060GRIN2Ac.3350T>A (p.Ile1117Asn)
c.2879T>A (p.Ile960Asn)
n.2943T>A
c.*720T>A (n.*720T>A)
c.2939T>A (p.Ile980Asn)
n.2989T>A
c.3191T>A (p.Ile1064Asn)
c.3092T>A (p.Ile1031Asn)
c.3506T>A (p.Ile1169Asn)
 dbSNP
16g.9764195T>ACA394708063GRIN2Ac.3349A>T (p.Ile1117Phe)
c.2878A>T (p.Ile960Phe)
n.2942A>T
c.*719A>T (n.*719A>T)
c.2938A>T (p.Ile980Phe)
n.2988A>T
c.3190A>T (p.Ile1064Phe)
c.3091A>T (p.Ile1031Phe)
c.3505A>T (p.Ile1169Phe)
 ClinVar dbSNP
16g.9764195T>CCA394708064GRIN2Ac.3349A>G (p.Ile1117Val)
c.2878A>G (p.Ile960Val)
n.2942A>G
c.*719A>G (n.*719A>G)
c.2938A>G (p.Ile980Val)
n.2988A>G
c.3190A>G (p.Ile1064Val)
c.3091A>G (p.Ile1031Val)
c.3505A>G (p.Ile1169Val)
16g.9764195T>GCA394708065GRIN2Ac.3349A>C (p.Ile1117Leu)
c.2878A>C (p.Ile960Leu)
n.2942A>C
c.*719A>C (n.*719A>C)
c.2938A>C (p.Ile980Leu)
n.2988A>C
c.3190A>C (p.Ile1064Leu)
c.3091A>C (p.Ile1031Leu)
c.3505A>C (p.Ile1169Leu)
 dbSNP
16g.9764198_9764204delCA974532105GRIN2Ac.3343_3349del (p.Asp1115SerfsTer4)
c.2872_2878del (p.Asp958SerfsTer4)
n.2936_2942del
c.*713_*719del (n.*713_*719del)
c.2932_2938del (p.Asp978SerfsTer4)
n.2982_2988del
c.3184_3190del (p.Asp1062SerfsTer4)
c.3085_3091del (p.Asp1029SerfsTer4)
c.3499_3505del (p.Asp1167SerfsTer4)
 gnomAD v3 gnomAD v4
16g.9764196C>ACA394708066GRIN2Ac.3348G>T (p.Lys1116Asn)
c.2877G>T (p.Lys959Asn)
n.2941G>T
c.*718G>T (n.*718G>T)
c.2937G>T (p.Lys979Asn)
n.2987G>T
c.3189G>T (p.Lys1063Asn)
c.3090G>T (p.Lys1030Asn)
c.3504G>T (p.Lys1168Asn)
 dbSNP gnomAD v4 COSMIC
16g.9764196C=CA2206693099GRIN2Ac.3348G= (p.Lys1116=)
c.2877G= (p.Lys959=)
n.2941G=
c.*718G= (n.*718G=)
c.2937G= (p.Lys979=)
n.2987G=
c.3189G= (p.Lys1063=)
c.3090G= (p.Lys1030=)
c.3504G= (p.Lys1168=)
16g.9764196C>GCA394708067GRIN2Ac.3348G>C (p.Lys1116Asn)
c.2877G>C (p.Lys959Asn)
n.2941G>C
c.*718G>C (n.*718G>C)
c.2937G>C (p.Lys979Asn)
n.2987G>C
c.3189G>C (p.Lys1063Asn)
c.3090G>C (p.Lys1030Asn)
c.3504G>C (p.Lys1168Asn)
 dbSNP
16g.9764196C>TCA7896332GRIN2Ac.3348G>A (p.Lys1116=)
c.2877G>A (p.Lys959=)
n.2941G>A
c.*718G>A (n.*718G>A)
c.2937G>A (p.Lys979=)
n.2987G>A
c.3189G>A (p.Lys1063=)
c.3090G>A (p.Lys1030=)
c.3504G>A (p.Lys1168=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.9764196_9764199delinsCTTGCA2206693100GRIN2Ac.3345_3348delinsCAAG (p.Asp1115=)
c.2874_2877delinsCAAG (p.Asp958=)
n.2938_2941delinsCAAG
c.*715_*718delinsCAAG (n.*715_*718delinsCAAG)
c.2934_2937delinsCAAG (p.Asp978=)
n.2984_2987delinsCAAG
c.3186_3189delinsCAAG (p.Asp1062=)
c.3087_3090delinsCAAG (p.Asp1029=)
c.3501_3504delinsCAAG (p.Asp1167=)
16g.9764196_9764197insACGGCA974532112GRIN2Ac.3347_3348insCCGT (p.Lys1116AsnfsTer9)
c.2876_2877insCCGT (p.Lys959AsnfsTer9)
n.2940_2941insCCGT
c.*717_*718insCCGT (n.*717_*718insCCGT)
c.2936_2937insCCGT (p.Lys979AsnfsTer9)
n.2986_2987insCCGT
c.3188_3189insCCGT (p.Lys1063AsnfsTer9)
c.3089_3090insCCGT (p.Lys1030AsnfsTer9)
c.3503_3504insCCGT (p.Lys1168AsnfsTer9)
16g.9764197T>ACA394708070GRIN2Ac.3347A>T (p.Lys1116Met)
c.2876A>T (p.Lys959Met)
n.2940A>T
c.*717A>T (n.*717A>T)
c.2936A>T (p.Lys979Met)
n.2986A>T
c.3188A>T (p.Lys1063Met)
c.3089A>T (p.Lys1030Met)
c.3503A>T (p.Lys1168Met)
 dbSNP
16g.9764197T>CCA394708068GRIN2Ac.3347A>G (p.Lys1116Arg)
c.2876A>G (p.Lys959Arg)
n.2940A>G
c.*717A>G (n.*717A>G)
c.2936A>G (p.Lys979Arg)
n.2986A>G
c.3188A>G (p.Lys1063Arg)
c.3089A>G (p.Lys1030Arg)
c.3503A>G (p.Lys1168Arg)
 COSMIC
16g.9764197T>GCA394708069GRIN2Ac.3347A>C (p.Lys1116Thr)
c.2876A>C (p.Lys959Thr)
n.2940A>C
c.*717A>C (n.*717A>C)
c.2936A>C (p.Lys979Thr)
n.2986A>C
c.3188A>C (p.Lys1063Thr)
c.3089A>C (p.Lys1030Thr)
c.3503A>C (p.Lys1168Thr)
 gnomAD v4 COSMIC
16g.9764197T=CA2206693101GRIN2Ac.3347A= (p.Lys1116=)
c.2876A= (p.Lys959=)
n.2940A=
c.*717A= (n.*717A=)
c.2936A= (p.Lys979=)
n.2986A=
c.3188A= (p.Lys1063=)
c.3089A= (p.Lys1030=)
c.3503A= (p.Lys1168=)
16g.9764197_9764198insCGGTCA974532113GRIN2Ac.3347_3348insCCGA (p.Lys1116AsnfsTer9)
c.2876_2877insCCGA (p.Lys959AsnfsTer9)
n.2940_2941insCCGA
c.*717_*718insCCGA (n.*717_*718insCCGA)
c.2936_2937insCCGA (p.Lys979AsnfsTer9)
n.2986_2987insCCGA
c.3188_3189insCCGA (p.Lys1063AsnfsTer9)
c.3089_3090insCCGA (p.Lys1030AsnfsTer9)
c.3503_3504insCCGA (p.Lys1168AsnfsTer9)
 gnomAD v3 gnomAD v4
16g.9764197_9764198insCGTTCA974532117GRIN2Ac.3347_3348insACGA (p.Ile1117ArgfsTer8)
c.2876_2877insACGA (p.Ile960ArgfsTer8)
n.2940_2941insACGA
c.*717_*718insACGA (n.*717_*718insACGA)
c.2936_2937insACGA (p.Ile980ArgfsTer8)
n.2986_2987insACGA
c.3188_3189insACGA (p.Ile1064ArgfsTer8)
c.3089_3090insACGA (p.Ile1031ArgfsTer8)
c.3503_3504insACGA (p.Ile1169ArgfsTer8)
 gnomAD v3 gnomAD v4
16g.9764198_9764200delCA621175127GRIN2Ac.3345_3347del (p.Asp1115_Lys1116delinsGlu)
c.2874_2876del (p.Asp958_Lys959delinsGlu)
n.2938_2940del
c.*715_*717del (n.*715_*717del)
c.2934_2936del (p.Asp978_Lys979delinsGlu)
n.2984_2986del
c.3186_3188del (p.Asp1062_Lys1063delinsGlu)
c.3087_3089del (p.Asp1029_Lys1030delinsGlu)
c.3501_3503del (p.Asp1167_Lys1168delinsGlu)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.9764197_9764198insCGCA974532145GRIN2Ac.3346_3347insCG (p.Lys1116ThrfsTer6)
c.2875_2876insCG (p.Lys959ThrfsTer6)
n.2939_2940insCG
c.*716_*717insCG (n.*716_*717insCG)
c.2935_2936insCG (p.Lys979ThrfsTer6)
n.2985_2986insCG
c.3187_3188insCG (p.Lys1063ThrfsTer6)
c.3088_3089insCG (p.Lys1030ThrfsTer6)
c.3502_3503insCG (p.Lys1168ThrfsTer6)
 gnomAD v3 gnomAD v4
16g.9764197_9764198insCGACA974532146GRIN2Ac.3346_3347insTCG (p.Lys1116delinsIleGlu)
c.2875_2876insTCG (p.Lys959delinsIleGlu)
n.2939_2940insTCG
c.*716_*717insTCG (n.*716_*717insTCG)
c.2935_2936insTCG (p.Lys979delinsIleGlu)
n.2985_2986insTCG
c.3187_3188insTCG (p.Lys1063delinsIleGlu)
c.3088_3089insTCG (p.Lys1030delinsIleGlu)
c.3502_3503insTCG (p.Lys1168delinsIleGlu)
 gnomAD v3 gnomAD v4
16g.9764197_9764198insCGGCA621175128GRIN2Ac.3346_3347insCCG (p.Lys1116delinsThrGlu)
c.2875_2876insCCG (p.Lys959delinsThrGlu)
n.2939_2940insCCG
c.*716_*717insCCG (n.*716_*717insCCG)
c.2935_2936insCCG (p.Lys979delinsThrGlu)
n.2985_2986insCCG
c.3187_3188insCCG (p.Lys1063delinsThrGlu)
c.3088_3089insCCG (p.Lys1030delinsThrGlu)
c.3502_3503insCCG (p.Lys1168delinsThrGlu)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.9764197_9764198insCGGTGGCA974532141GRIN2Ac.3346_3347insCCACCG (p.Lys1116delinsThrThrGlu)
c.2875_2876insCCACCG (p.Lys959delinsThrThrGlu)
n.2939_2940insCCACCG
c.*716_*717insCCACCG (n.*716_*717insCCACCG)
c.2935_2936insCCACCG (p.Lys979delinsThrThrGlu)
n.2985_2986insCCACCG
c.3187_3188insCCACCG (p.Lys1063delinsThrThrGlu)
c.3088_3089insCCACCG (p.Lys1030delinsThrThrGlu)
c.3502_3503insCCACCG (p.Lys1168delinsThrThrGlu)
 gnomAD v3 gnomAD v4
16g.9764197_9764198insCGGTGGTCGCCGCA974532148GRIN2Ac.3346_3347insCGGCGACCACCG (p.Lys1116delinsThrAlaThrThrGlu)
c.2875_2876insCGGCGACCACCG (p.Lys959delinsThrAlaThrThrGlu)
n.2939_2940insCGGCGACCACCG
c.*716_*717insCGGCGACCACCG (n.*716_*717insCGGCGACCACCG)
c.2935_2936insCGGCGACCACCG (p.Lys979delinsThrAlaThrThrGlu)
n.2985_2986insCGGCGACCACCG
c.3187_3188insCGGCGACCACCG (p.Lys1063delinsThrAlaThrThrGlu)
c.3088_3089insCGGCGACCACCG (p.Lys1030delinsThrAlaThrThrGlu)
c.3502_3503insCGGCGACCACCG (p.Lys1168delinsThrAlaThrThrGlu)
 gnomAD v3 gnomAD v4
16g.9764197_9764198insCGGTGGTCGCCGTATCATTAAAAAACA974532138GRIN2Ac.3346_3347insTTTTTTAATGATACGGCGACCACCG (p.Lys1116IlefsTer3)
c.2875_2876insTTTTTTAATGATACGGCGACCACCG (p.Lys959IlefsTer3)
n.2939_2940insTTTTTTAATGATACGGCGACCACCG
c.*716_*717insTTTTTTAATGATACGGCGACCACCG (n.*716_*717insTTTTTTAATGATACGGCGACCACCG)
c.2935_2936insTTTTTTAATGATACGGCGACCACCG (p.Lys979IlefsTer3)
n.2985_2986insTTTTTTAATGATACGGCGACCACCG
c.3187_3188insTTTTTTAATGATACGGCGACCACCG (p.Lys1063IlefsTer3)
c.3088_3089insTTTTTTAATGATACGGCGACCACCG (p.Lys1030IlefsTer3)
c.3502_3503insTTTTTTAATGATACGGCGACCACCG (p.Lys1168IlefsTer3)
 gnomAD v3 gnomAD v4
16g.9764197_9764198insCGGTGGTCGCCGTATCATTAAAAAAACA974532135GRIN2Ac.3346_3347insTTTTTTTAATGATACGGCGACCACCG (p.Lys1116IlefsTer14)
c.2875_2876insTTTTTTTAATGATACGGCGACCACCG (p.Lys959IlefsTer14)
n.2939_2940insTTTTTTTAATGATACGGCGACCACCG
c.*716_*717insTTTTTTTAATGATACGGCGACCACCG (n.*716_*717insTTTTTTTAATGATACGGCGACCACCG)
c.2935_2936insTTTTTTTAATGATACGGCGACCACCG (p.Lys979IlefsTer14)
n.2985_2986insTTTTTTTAATGATACGGCGACCACCG
c.3187_3188insTTTTTTTAATGATACGGCGACCACCG (p.Lys1063IlefsTer14)
c.3088_3089insTTTTTTTAATGATACGGCGACCACCG (p.Lys1030IlefsTer14)
c.3502_3503insTTTTTTTAATGATACGGCGACCACCG (p.Lys1168IlefsTer14)
 gnomAD v3 gnomAD v4
16g.9764197_9764198insCGGTGGTCGCCGTATCATTAAAAAATTTCACA974532132GRIN2Ac.3346_3347insTGAAATTTTTTAATGATACGGCGACCACCG (p.Lys1116delinsMetLysPhePheAsnAspThrAlaThrThrGlu)
c.2875_2876insTGAAATTTTTTAATGATACGGCGACCACCG (p.Lys959delinsMetLysPhePheAsnAspThrAlaThrThrGlu)
n.2939_2940insTGAAATTTTTTAATGATACGGCGACCACCG
c.*716_*717insTGAAATTTTTTAATGATACGGCGACCACCG (n.*716_*717insTGAAATTTTTTAATGATACGGCGACCACCG)
c.2935_2936insTGAAATTTTTTAATGATACGGCGACCACCG (p.Lys979delinsMetLysPhePheAsnAspThrAlaThrThrGlu)
n.2985_2986insTGAAATTTTTTAATGATACGGCGACCACCG
c.3187_3188insTGAAATTTTTTAATGATACGGCGACCACCG (p.Lys1063delinsMetLysPhePheAsnAspThrAlaThrThrGlu)
c.3088_3089insTGAAATTTTTTAATGATACGGCGACCACCG (p.Lys1030delinsMetLysPhePheAsnAspThrAlaThrThrGlu)
c.3502_3503insTGAAATTTTTTAATGATACGGCGACCACCG (p.Lys1168delinsMetLysPhePheAsnAspThrAlaThrThrGlu)
 gnomAD v3 gnomAD v4
16g.9764198T>ACA394708071GRIN2Ac.3346A>T (p.Lys1116Ter)
c.2875A>T (p.Lys959Ter)
n.2939A>T
c.*716A>T (n.*716A>T)
c.2935A>T (p.Lys979Ter)
n.2985A>T
c.3187A>T (p.Lys1063Ter)
c.3088A>T (p.Lys1030Ter)
c.3502A>T (p.Lys1168Ter)
 dbSNP COSMIC
16g.9764198T>CCA394708072GRIN2Ac.3346A>G (p.Lys1116Glu)
c.2875A>G (p.Lys959Glu)
n.2939A>G
c.*716A>G (n.*716A>G)
c.2935A>G (p.Lys979Glu)
n.2985A>G
c.3187A>G (p.Lys1063Glu)
c.3088A>G (p.Lys1030Glu)
c.3502A>G (p.Lys1168Glu)
 dbSNP gnomAD v3 gnomAD v4
16g.9764198T>GCA394708073GRIN2Ac.3346A>C (p.Lys1116Gln)
c.2875A>C (p.Lys959Gln)
n.2939A>C
c.*716A>C (n.*716A>C)
c.2935A>C (p.Lys979Gln)
n.2985A>C
c.3187A>C (p.Lys1063Gln)
c.3088A>C (p.Lys1030Gln)
c.3502A>C (p.Lys1168Gln)
16g.9764198T=CA2206693102GRIN2Ac.3346A= (p.Lys1116=)
c.2875A= (p.Lys959=)
n.2939A=
c.*716A= (n.*716A=)
c.2935A= (p.Lys979=)
n.2985A=
c.3187A= (p.Lys1063=)
c.3088A= (p.Lys1030=)
c.3502A= (p.Lys1168=)
16g.9764198_9764199insTGCA974532168GRIN2Ac.3345_3346insCA (p.Lys1116GlnfsTer6)
c.2874_2875insCA (p.Lys959GlnfsTer6)
n.2938_2939insCA
c.*715_*716insCA (n.*715_*716insCA)
c.2934_2935insCA (p.Lys979GlnfsTer6)
n.2984_2985insCA
c.3186_3187insCA (p.Lys1063GlnfsTer6)
c.3087_3088insCA (p.Lys1030GlnfsTer6)
c.3501_3502insCA (p.Lys1168GlnfsTer6)
 gnomAD v3 gnomAD v4
16g.9764199G>ACA493692984GRIN2Ac.3345C>T (p.Asp1115=)
c.2874C>T (p.Asp958=)
n.2938C>T
c.*715C>T (n.*715C>T)
c.2934C>T (p.Asp978=)
n.2984C>T
c.3186C>T (p.Asp1062=)
c.3087C>T (p.Asp1029=)
c.3501C>T (p.Asp1167=)
 ClinVar
16g.9764199G>CCA277537425GRIN2Ac.3345C>G (p.Asp1115Glu)
c.2874C>G (p.Asp958Glu)
n.2938C>G
c.*715C>G (n.*715C>G)
c.2934C>G (p.Asp978Glu)
n.2984C>G
c.3186C>G (p.Asp1062Glu)
c.3087C>G (p.Asp1029Glu)
c.3501C>G (p.Asp1167Glu)
 ClinVar dbSNP
16g.9764199G=CA2206693103GRIN2Ac.3345C= (p.Asp1115=)
c.2874C= (p.Asp958=)
n.2938C=
c.*715C= (n.*715C=)
c.2934C= (p.Asp978=)
n.2984C=
c.3186C= (p.Asp1062=)
c.3087C= (p.Asp1029=)
c.3501C= (p.Asp1167=)
16g.9764199G>TCA7896333GRIN2Ac.3345C>A (p.Asp1115Glu)
c.2874C>A (p.Asp958Glu)
n.2938C>A
c.*715C>A (n.*715C>A)
c.2934C>A (p.Asp978Glu)
n.2984C>A
c.3186C>A (p.Asp1062Glu)
c.3087C>A (p.Asp1029Glu)
c.3501C>A (p.Asp1167Glu)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.9764199_9764200insGTGGCA2631675661GRIN2Ac.3345_3346insCACC (p.Lys1116HisfsTer9)
c.2874_2875insCACC (p.Lys959HisfsTer9)
n.2938_2939insCACC
c.*715_*716insCACC (n.*715_*716insCACC)
c.2934_2935insCACC (p.Lys979HisfsTer9)
n.2984_2985insCACC
c.3186_3187insCACC (p.Lys1063HisfsTer9)
c.3087_3088insCACC (p.Lys1030HisfsTer9)
c.3501_3502insCACC (p.Lys1168HisfsTer9)
 gnomAD v4
16g.9764199dupCA621175129GRIN2Ac.3345dup (p.Lys1116GlnfsTer8)
c.2874dup (p.Lys959GlnfsTer8)
n.2938dup
c.*715dup (n.*715dup)
c.2934dup (p.Lys979GlnfsTer8)
n.2984dup
c.3186dup (p.Lys1063GlnfsTer8)
c.3087dup (p.Lys1030GlnfsTer8)
c.3501dup (p.Lys1168GlnfsTer8)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.9764199_9764217delinsGTCTCTAGGGGAGCTTGATCA2206693104GRIN2Ac.3327_3345delinsATCAAGCTCCCCTAGAGAC (p.Lys1109=)
c.2856_2874delinsATCAAGCTCCCCTAGAGAC (p.Lys952=)
n.2920_2938delinsATCAAGCTCCCCTAGAGAC
c.*697_*715delinsATCAAGCTCCCCTAGAGAC (n.*697_*715delinsATCAAGCTCCCCTAGAGAC)
c.2916_2934delinsATCAAGCTCCCCTAGAGAC (p.Lys972=)
n.2966_2984delinsATCAAGCTCCCCTAGAGAC
c.3168_3186delinsATCAAGCTCCCCTAGAGAC (p.Lys1056=)
c.3069_3087delinsATCAAGCTCCCCTAGAGAC (p.Lys1023=)
c.3483_3501delinsATCAAGCTCCCCTAGAGAC (p.Lys1161=)
16g.9764199_9764200insGTCGCCGTACA974532188GRIN2Ac.3344_3345insTACGGCGAC (p.Asp1115_Lys1116insThrAlaThr)
c.2873_2874insTACGGCGAC (p.Asp958_Lys959insThrAlaThr)
n.2937_2938insTACGGCGAC
c.*714_*715insTACGGCGAC (n.*714_*715insTACGGCGAC)
c.2933_2934insTACGGCGAC (p.Asp978_Lys979insThrAlaThr)
n.2983_2984insTACGGCGAC
c.3185_3186insTACGGCGAC (p.Asp1062_Lys1063insThrAlaThr)
c.3086_3087insTACGGCGAC (p.Asp1029_Lys1030insThrAlaThr)
c.3500_3501insTACGGCGAC (p.Asp1167_Lys1168insThrAlaThr)
 gnomAD v3 gnomAD v4
16g.9764199_9764200insGTCGCCGTATCATTAAAAAATTCA974532186GRIN2Ac.3344_3345insAATTTTTTAATGATACGGCGAC (p.Asp1115GlufsTer4)
c.2873_2874insAATTTTTTAATGATACGGCGAC (p.Asp958GlufsTer4)
n.2937_2938insAATTTTTTAATGATACGGCGAC
c.*714_*715insAATTTTTTAATGATACGGCGAC (n.*714_*715insAATTTTTTAATGATACGGCGAC)
c.2933_2934insAATTTTTTAATGATACGGCGAC (p.Asp978GlufsTer4)
n.2983_2984insAATTTTTTAATGATACGGCGAC
c.3185_3186insAATTTTTTAATGATACGGCGAC (p.Asp1062GlufsTer4)
c.3086_3087insAATTTTTTAATGATACGGCGAC (p.Asp1029GlufsTer4)
c.3500_3501insAATTTTTTAATGATACGGCGAC (p.Asp1167GlufsTer4)
 gnomAD v3 gnomAD v4
16g.9764200delCA974532184GRIN2Ac.3344del (p.Asp1115AlafsTer6)
c.2873del (p.Asp958AlafsTer6)
n.2937del
c.*714del (n.*714del)
c.2933del (p.Asp978AlafsTer6)
n.2983del
c.3185del (p.Asp1062AlafsTer6)
c.3086del (p.Asp1029AlafsTer6)
c.3500del (p.Asp1167AlafsTer6)
 gnomAD v3 gnomAD v4
16g.9764200T>ACA314974GRIN2Ac.3344A>T (p.Asp1115Val)
c.2873A>T (p.Asp958Val)
n.2937A>T
c.*714A>T (n.*714A>T)
c.2933A>T (p.Asp978Val)
n.2983A>T
c.3185A>T (p.Asp1062Val)
c.3086A>T (p.Asp1029Val)
c.3500A>T (p.Asp1167Val)
 ClinVar dbSNP
16g.9764200T>CCA394708075GRIN2Ac.3344A>G (p.Asp1115Gly)
c.2873A>G (p.Asp958Gly)
n.2937A>G
c.*714A>G (n.*714A>G)
c.2933A>G (p.Asp978Gly)
n.2983A>G
c.3185A>G (p.Asp1062Gly)
c.3086A>G (p.Asp1029Gly)
c.3500A>G (p.Asp1167Gly)
 dbSNP gnomAD v2 gnomAD v4
16g.9764200T>GCA394708074GRIN2Ac.3344A>C (p.Asp1115Ala)
c.2873A>C (p.Asp958Ala)
n.2937A>C
c.*714A>C (n.*714A>C)
c.2933A>C (p.Asp978Ala)
n.2983A>C
c.3185A>C (p.Asp1062Ala)
c.3086A>C (p.Asp1029Ala)
c.3500A>C (p.Asp1167Ala)
 gnomAD v3 gnomAD v4
16g.9764200T=CA2206693105GRIN2Ac.3344A= (p.Asp1115=)
c.2873A= (p.Asp958=)
n.2937A=
c.*714A= (n.*714A=)
c.2933A= (p.Asp978=)
n.2983A=
c.3185A= (p.Asp1062=)
c.3086A= (p.Asp1029=)
c.3500A= (p.Asp1167=)
16g.9764200_9764202delCA974532177GRIN2Ac.3342_3344del (p.Arg1114_Asp1115delinsSer)
c.2871_2873del (p.Arg957_Asp958delinsSer)
n.2935_2937del
c.*712_*714del (n.*712_*714del)
c.2931_2933del (p.Arg977_Asp978delinsSer)
n.2981_2983del
c.3183_3185del (p.Arg1061_Asp1062delinsSer)
c.3084_3086del (p.Arg1028_Asp1029delinsSer)
c.3498_3500del (p.Arg1166_Asp1167delinsSer)
 gnomAD v3 gnomAD v4
16g.9764200_9764205delCA974532182GRIN2Ac.3339_3344del (p.Arg1114_Asp1115del)
c.2868_2873del (p.Arg957_Asp958del)
n.2932_2937del
c.*709_*714del (n.*709_*714del)
c.2928_2933del (p.Arg977_Asp978del)
n.2978_2983del
c.3180_3185del (p.Arg1061_Asp1062del)
c.3081_3086del (p.Arg1028_Asp1029del)
c.3495_3500del (p.Arg1166_Asp1167del)
 gnomAD v3 gnomAD v4
16g.9764201_9764218delCA974532181GRIN2Ac.3327_3344del (p.Lys1109_Asp1115delinsAsn)
c.2856_2873del (p.Lys952_Asp958delinsAsn)
n.2920_2937del
c.*697_*714del (n.*697_*714del)
c.2916_2933del (p.Lys972_Asp978delinsAsn)
n.2966_2983del
c.3168_3185del (p.Lys1056_Asp1062delinsAsn)
c.3069_3086del (p.Lys1023_Asp1029delinsAsn)
c.3483_3500del (p.Lys1161_Asp1167delinsAsn)
 dbSNP gnomAD v3 gnomAD v4
16g.9764200_9764201insTGCA974532194GRIN2Ac.3343_3344insCA (p.Asp1115AlafsTer7)
c.2872_2873insCA (p.Asp958AlafsTer7)
n.2936_2937insCA
c.*713_*714insCA (n.*713_*714insCA)
c.2932_2933insCA (p.Asp978AlafsTer7)
n.2982_2983insCA
c.3184_3185insCA (p.Asp1062AlafsTer7)
c.3085_3086insCA (p.Asp1029AlafsTer7)
c.3499_3500insCA (p.Asp1167AlafsTer7)
 gnomAD v3 gnomAD v4
16g.9764201delCA974532196GRIN2Ac.3343del (p.Asp1115ThrfsTer6)
c.2872del (p.Asp958ThrfsTer6)
n.2936del
c.*713del (n.*713del)
c.2932del (p.Asp978ThrfsTer6)
n.2982del
c.3184del (p.Asp1062ThrfsTer6)
c.3085del (p.Asp1029ThrfsTer6)
c.3499del (p.Asp1167ThrfsTer6)
 gnomAD v3 gnomAD v4
16g.9764201C>ACA394708076GRIN2Ac.3343G>T (p.Asp1115Tyr)
c.2872G>T (p.Asp958Tyr)
n.2936G>T
c.*713G>T (n.*713G>T)
c.2932G>T (p.Asp978Tyr)
n.2982G>T
c.3184G>T (p.Asp1062Tyr)
c.3085G>T (p.Asp1029Tyr)
c.3499G>T (p.Asp1167Tyr)
16g.9764201C=CA2206693106GRIN2Ac.3343G= (p.Asp1115=)
c.2872G= (p.Asp958=)
n.2936G=
c.*713G= (n.*713G=)
c.2932G= (p.Asp978=)
n.2982G=
c.3184G= (p.Asp1062=)
c.3085G= (p.Asp1029=)
c.3499G= (p.Asp1167=)
16g.9764201C>GCA277537427GRIN2Ac.3343G>C (p.Asp1115His)
c.2872G>C (p.Asp958His)
n.2936G>C
c.*713G>C (n.*713G>C)
c.2932G>C (p.Asp978His)
n.2982G>C
c.3184G>C (p.Asp1062His)
c.3085G>C (p.Asp1029His)
c.3499G>C (p.Asp1167His)
 ClinVar dbSNP gnomAD v4
16g.9764201C>TCA394708077GRIN2Ac.3343G>A (p.Asp1115Asn)
c.2872G>A (p.Asp958Asn)
n.2936G>A
c.*713G>A (n.*713G>A)
c.2932G>A (p.Asp978Asn)
n.2982G>A
c.3184G>A (p.Asp1062Asn)
c.3085G>A (p.Asp1029Asn)
c.3499G>A (p.Asp1167Asn)
 gnomAD v3 gnomAD v4
16g.9764201_9764202insGCCA2553742910GRIN2Ac.3343_3344insCG (p.Asp1115AlafsTer7)
c.2872_2873insCG (p.Asp958AlafsTer7)
n.2936_2937insCG
c.*713_*714insCG (n.*713_*714insCG)
c.2932_2933insCG (p.Asp978AlafsTer7)
n.2982_2983insCG
c.3184_3185insCG (p.Asp1062AlafsTer7)
c.3085_3086insCG (p.Asp1029AlafsTer7)
c.3499_3500insCG (p.Asp1167AlafsTer7)
16g.9764201_9764205delinsCTCTACA2206693107GRIN2Ac.3339_3343delinsTAGAG (p.Pro1113=)
c.2868_2872delinsTAGAG (p.Pro956=)
n.2932_2936delinsTAGAG
c.*709_*713delinsTAGAG (n.*709_*713delinsTAGAG)
c.2928_2932delinsTAGAG (p.Pro976=)
n.2978_2982delinsTAGAG
c.3180_3184delinsTAGAG (p.Pro1060=)
c.3081_3085delinsTAGAG (p.Pro1027=)
c.3495_3499delinsTAGAG (p.Pro1165=)
16g.9764201_9764202insGGCA974532212GRIN2Ac.3342_3343insCC (p.Asp1115ProfsTer7)
c.2871_2872insCC (p.Asp958ProfsTer7)
n.2935_2936insCC
c.*712_*713insCC (n.*712_*713insCC)
c.2931_2932insCC (p.Asp978ProfsTer7)
n.2981_2982insCC
c.3183_3184insCC (p.Asp1062ProfsTer7)
c.3084_3085insCC (p.Asp1029ProfsTer7)
c.3498_3499insCC (p.Asp1167ProfsTer7)
 gnomAD v3 gnomAD v4
16g.9764201_9764202insGCCGTACA974532203GRIN2Ac.3342_3343insTACGGC (p.Arg1114_Asp1115insTyrGly)
c.2871_2872insTACGGC (p.Arg957_Asp958insTyrGly)
n.2935_2936insTACGGC
c.*712_*713insTACGGC (n.*712_*713insTACGGC)
c.2931_2932insTACGGC (p.Arg977_Asp978insTyrGly)
n.2981_2982insTACGGC
c.3183_3184insTACGGC (p.Arg1061_Asp1062insTyrGly)
c.3084_3085insTACGGC (p.Arg1028_Asp1029insTyrGly)
c.3498_3499insTACGGC (p.Arg1166_Asp1167insTyrGly)
 gnomAD v3 gnomAD v4
16g.9764202T>ACA394708078GRIN2Ac.3342A>T (p.Arg1114Ser)
c.2871A>T (p.Arg957Ser)
n.2935A>T
c.*712A>T (n.*712A>T)
c.2931A>T (p.Arg977Ser)
n.2981A>T
c.3183A>T (p.Arg1061Ser)
c.3084A>T (p.Arg1028Ser)
c.3498A>T (p.Arg1166Ser)
 dbSNP
16g.9764202T>CCA493692989GRIN2Ac.3342A>G (p.Arg1114=)
c.2871A>G (p.Arg957=)
n.2935A>G
c.*712A>G (n.*712A>G)
c.2931A>G (p.Arg977=)
n.2981A>G
c.3183A>G (p.Arg1061=)
c.3084A>G (p.Arg1028=)
c.3498A>G (p.Arg1166=)
 dbSNP
16g.9764202T>GCA394708079GRIN2Ac.3342A>C (p.Arg1114Ser)
c.2871A>C (p.Arg957Ser)
n.2935A>C
c.*712A>C (n.*712A>C)
c.2931A>C (p.Arg977Ser)
n.2981A>C
c.3183A>C (p.Arg1061Ser)
c.3084A>C (p.Arg1028Ser)
c.3498A>C (p.Arg1166Ser)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.9764202T=CA2206693108GRIN2Ac.3342A= (p.Arg1114=)
c.2871A= (p.Arg957=)
n.2935A=
c.*712A= (n.*712A=)
c.2931A= (p.Arg977=)
n.2981A=
c.3183A= (p.Arg1061=)
c.3084A= (p.Arg1028=)
c.3498A= (p.Arg1166=)
16g.9764202_9764205delCA621175130GRIN2Ac.3339_3342del (p.Arg1114ThrfsTer6)
c.2868_2871del (p.Arg957ThrfsTer6)
n.2932_2935del
c.*709_*712del (n.*709_*712del)
c.2928_2931del (p.Arg977ThrfsTer6)
n.2978_2981del
c.3180_3183del (p.Arg1061ThrfsTer6)
c.3081_3084del (p.Arg1028ThrfsTer6)
c.3495_3498del (p.Arg1166ThrfsTer6)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.9764202_9764206delCA974532217GRIN2Ac.3338_3342del (p.Pro1113ArgfsTer9)
c.2867_2871del (p.Pro956ArgfsTer9)
n.2931_2935del
c.*708_*712del (n.*708_*712del)
c.2927_2931del (p.Pro976ArgfsTer9)
n.2977_2981del
c.3179_3183del (p.Pro1060ArgfsTer9)
c.3080_3084del (p.Pro1027ArgfsTer9)
c.3494_3498del (p.Pro1165ArgfsTer9)
 gnomAD v3 gnomAD v4
16g.9764202_9764207delCA974532206GRIN2Ac.3337_3342del (p.Pro1113_Arg1114del)
c.2866_2871del (p.Pro956_Arg957del)
n.2930_2935del
c.*707_*712del (n.*707_*712del)
c.2926_2931del (p.Pro976_Arg977del)
n.2976_2981del
c.3178_3183del (p.Pro1060_Arg1061del)
c.3079_3084del (p.Pro1027_Arg1028del)
c.3493_3498del (p.Pro1165_Arg1166del)
 gnomAD v3 gnomAD v4
16g.9764202_9764210delCA974532205GRIN2Ac.3334_3342del (p.Ser1112_Arg1114del)
c.2863_2871del (p.Ser955_Arg957del)
n.2927_2935del
c.*704_*712del (n.*704_*712del)
c.2923_2931del (p.Ser975_Arg977del)
n.2973_2981del
c.3175_3183del (p.Ser1059_Arg1061del)
c.3076_3084del (p.Ser1026_Arg1028del)
c.3490_3498del (p.Ser1164_Arg1166del)
 gnomAD v3 gnomAD v4
16g.9764203C>ACA394708080GRIN2Ac.3341G>T (p.Arg1114Ile)
c.2870G>T (p.Arg957Ile)
n.2934G>T
c.*711G>T (n.*711G>T)
c.2930G>T (p.Arg977Ile)
n.2980G>T
c.3182G>T (p.Arg1061Ile)
c.3083G>T (p.Arg1028Ile)
c.3497G>T (p.Arg1166Ile)
 dbSNP
16g.9764203C=CA2206693109GRIN2Ac.3341G= (p.Arg1114=)
c.2870G= (p.Arg957=)
n.2934G=
c.*711G= (n.*711G=)
c.2930G= (p.Arg977=)
n.2980G=
c.3182G= (p.Arg1061=)
c.3083G= (p.Arg1028=)
c.3497G= (p.Arg1166=)
16g.9764203C>GCA314972GRIN2Ac.3341G>C (p.Arg1114Thr)
c.2870G>C (p.Arg957Thr)
n.2934G>C
c.*711G>C (n.*711G>C)
c.2930G>C (p.Arg977Thr)
n.2980G>C
c.3182G>C (p.Arg1061Thr)
c.3083G>C (p.Arg1028Thr)
c.3497G>C (p.Arg1166Thr)
 ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
16g.9764203C>TCA394708081GRIN2Ac.3341G>A (p.Arg1114Lys)
c.2870G>A (p.Arg957Lys)
n.2934G>A
c.*711G>A (n.*711G>A)
c.2930G>A (p.Arg977Lys)
n.2980G>A
c.3182G>A (p.Arg1061Lys)
c.3083G>A (p.Arg1028Lys)
c.3497G>A (p.Arg1166Lys)
 dbSNP
16g.9764203_9764205delCA974532229GRIN2Ac.3339_3341del (p.Arg1114del)
c.2868_2870del (p.Arg957del)
n.2932_2934del
c.*709_*711del (n.*709_*711del)
c.2928_2930del (p.Arg977del)
n.2978_2980del
c.3180_3182del (p.Arg1061del)
c.3081_3083del (p.Arg1028del)
c.3495_3497del (p.Arg1166del)
 gnomAD v3 gnomAD v4
16g.9764203_9764206delCA974532230GRIN2Ac.3338_3341del (p.Pro1113GlnfsTer7)
c.2867_2870del (p.Pro956GlnfsTer7)
n.2931_2934del
c.*708_*711del (n.*708_*711del)
c.2927_2930del (p.Pro976GlnfsTer7)
n.2977_2980del
c.3179_3182del (p.Pro1060GlnfsTer7)
c.3080_3083del (p.Pro1027GlnfsTer7)
c.3494_3497del (p.Pro1165GlnfsTer7)
 gnomAD v3 gnomAD v4
16g.9764203_9764204insAGCA974532275GRIN2Ac.3340_3341insCT (p.Arg1114ThrfsTer8)
c.2869_2870insCT (p.Arg957ThrfsTer8)
n.2933_2934insCT
c.*710_*711insCT (n.*710_*711insCT)
c.2929_2930insCT (p.Arg977ThrfsTer8)
n.2979_2980insCT
c.3181_3182insCT (p.Arg1061ThrfsTer8)
c.3082_3083insCT (p.Arg1028ThrfsTer8)
c.3496_3497insCT (p.Arg1166ThrfsTer8)
 gnomAD v3 gnomAD v4
16g.9764203_9764204insATCA974532271GRIN2Ac.3340_3341insAT (p.Arg1114AsnfsTer8)
c.2869_2870insAT (p.Arg957AsnfsTer8)
n.2933_2934insAT
c.*710_*711insAT (n.*710_*711insAT)
c.2929_2930insAT (p.Arg977AsnfsTer8)
n.2979_2980insAT
c.3181_3182insAT (p.Arg1061AsnfsTer8)
c.3082_3083insAT (p.Arg1028AsnfsTer8)
c.3496_3497insAT (p.Arg1166AsnfsTer8)
 gnomAD v3 gnomAD v4
16g.9764203_9764204insCACA974532269GRIN2Ac.3340_3341insTG (p.Arg1114MetfsTer8)
c.2869_2870insTG (p.Arg957MetfsTer8)
n.2933_2934insTG
c.*710_*711insTG (n.*710_*711insTG)
c.2929_2930insTG (p.Arg977MetfsTer8)
n.2979_2980insTG
c.3181_3182insTG (p.Arg1061MetfsTer8)
c.3082_3083insTG (p.Arg1028MetfsTer8)
c.3496_3497insTG (p.Arg1166MetfsTer8)
 gnomAD v3 gnomAD v4
16g.9764203_9764204insCGCA621175131GRIN2Ac.3340_3341insCG (p.Arg1114ThrfsTer8)
c.2869_2870insCG (p.Arg957ThrfsTer8)
n.2933_2934insCG
c.*710_*711insCG (n.*710_*711insCG)
c.2929_2930insCG (p.Arg977ThrfsTer8)
n.2979_2980insCG
c.3181_3182insCG (p.Arg1061ThrfsTer8)
c.3082_3083insCG (p.Arg1028ThrfsTer8)
c.3496_3497insCG (p.Arg1166ThrfsTer8)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.9764203_9764204insGCCGCA974532265GRIN2Ac.3340_3341insCGGC (p.Arg1114ThrfsTer11)
c.2869_2870insCGGC (p.Arg957ThrfsTer11)
n.2933_2934insCGGC
c.*710_*711insCGGC (n.*710_*711insCGGC)
c.2929_2930insCGGC (p.Arg977ThrfsTer11)
n.2979_2980insCGGC
c.3181_3182insCGGC (p.Arg1061ThrfsTer11)
c.3082_3083insCGGC (p.Arg1028ThrfsTer11)
c.3496_3497insCGGC (p.Arg1166ThrfsTer11)
 gnomAD v3 gnomAD v4
16g.9764204delCA974532264GRIN2Ac.3340del (p.Arg1114GlufsTer7)
c.2869del (p.Arg957GlufsTer7)
n.2933del
c.*710del (n.*710del)
c.2929del (p.Arg977GlufsTer7)
n.2979del
c.3181del (p.Arg1061GlufsTer7)
c.3082del (p.Arg1028GlufsTer7)
c.3496del (p.Arg1166GlufsTer7)
 gnomAD v3 gnomAD v4
16g.9764204T>ACA394708082GRIN2Ac.3340A>T (p.Arg1114Ter)
c.2869A>T (p.Arg957Ter)
n.2933A>T
c.*710A>T (n.*710A>T)
c.2929A>T (p.Arg977Ter)
n.2979A>T
c.3181A>T (p.Arg1061Ter)
c.3082A>T (p.Arg1028Ter)
c.3496A>T (p.Arg1166Ter)
 dbSNP
16g.9764204T>CCA394708083GRIN2Ac.3340A>G (p.Arg1114Gly)
c.2869A>G (p.Arg957Gly)
n.2933A>G
c.*710A>G (n.*710A>G)
c.2929A>G (p.Arg977Gly)
n.2979A>G
c.3181A>G (p.Arg1061Gly)
c.3082A>G (p.Arg1028Gly)
c.3496A>G (p.Arg1166Gly)
 dbSNP
16g.9764204T>GCA493692992GRIN2Ac.3340A>C (p.Arg1114=)
c.2869A>C (p.Arg957=)
n.2933A>C
c.*710A>C (n.*710A>C)
c.2929A>C (p.Arg977=)
n.2979A>C
c.3181A>C (p.Arg1061=)
c.3082A>C (p.Arg1028=)
c.3496A>C (p.Arg1166=)
16g.9764204T=CA2206693110GRIN2Ac.3340A= (p.Arg1114=)
c.2869A= (p.Arg957=)
n.2933A=
c.*710A= (n.*710A=)
c.2929A= (p.Arg977=)
n.2979A=
c.3181A= (p.Arg1061=)
c.3082A= (p.Arg1028=)
c.3496A= (p.Arg1166=)
16g.9764204_9764206delCA974532246GRIN2Ac.3338_3340del (p.Pro1113del)
c.2867_2869del (p.Pro956del)
n.2931_2933del
c.*708_*710del (n.*708_*710del)
c.2927_2929del (p.Pro976del)
n.2977_2979del
c.3179_3181del (p.Pro1060del)
c.3080_3082del (p.Pro1027del)
c.3494_3496del (p.Pro1165del)
 gnomAD v3 gnomAD v4
16g.9764204_9764207delCA2511614264GRIN2Ac.3337_3340del (p.Pro1113GlufsTer7)
c.2866_2869del (p.Pro956GlufsTer7)
n.2930_2933del
c.*707_*710del (n.*707_*710del)
c.2926_2929del (p.Pro976GlufsTer7)
n.2976_2979del
c.3178_3181del (p.Pro1060GlufsTer7)
c.3079_3082del (p.Pro1027GlufsTer7)
c.3493_3496del (p.Pro1165GlufsTer7)
16g.9764204_9764210delCA974532239GRIN2Ac.3334_3340del (p.Ser1112GlufsTer7)
c.2863_2869del (p.Ser955GlufsTer7)
n.2927_2933del
c.*704_*710del (n.*704_*710del)
c.2923_2929del (p.Ser975GlufsTer7)
n.2973_2979del
c.3175_3181del (p.Ser1059GlufsTer7)
c.3076_3082del (p.Ser1026GlufsTer7)
c.3490_3496del (p.Ser1164GlufsTer7)
 gnomAD v3 gnomAD v4
16g.9764204_9764211delCA974532243GRIN2Ac.3333_3340del (p.Ser1111ArgfsTer10)
c.2862_2869del (p.Ser954ArgfsTer10)
n.2926_2933del
c.*703_*710del (n.*703_*710del)
c.2922_2929del (p.Ser974ArgfsTer10)
n.2972_2979del
c.3174_3181del (p.Ser1058ArgfsTer10)
c.3075_3082del (p.Ser1025ArgfsTer10)
c.3489_3496del (p.Ser1163ArgfsTer10)
 gnomAD v3 gnomAD v4
16g.9764205A>CCA493692993GRIN2Ac.3339T>G (p.Pro1113=)
c.2868T>G (p.Pro956=)
n.2932T>G
c.*709T>G (n.*709T>G)
c.2928T>G (p.Pro976=)
n.2978T>G
c.3180T>G (p.Pro1060=)
c.3081T>G (p.Pro1027=)
c.3495T>G (p.Pro1165=)
16g.9764205A>GCA493692994GRIN2Ac.3339T>C (p.Pro1113=)
c.2868T>C (p.Pro956=)
n.2932T>C
c.*709T>C (n.*709T>C)
c.2928T>C (p.Pro976=)
n.2978T>C
c.3180T>C (p.Pro1060=)
c.3081T>C (p.Pro1027=)
c.3495T>C (p.Pro1165=)
 ClinVar dbSNP
16g.9764205A>TCA493692995GRIN2Ac.3339T>A (p.Pro1113=)
c.2868T>A (p.Pro956=)
n.2932T>A
c.*709T>A (n.*709T>A)
c.2928T>A (p.Pro976=)
n.2978T>A
c.3180T>A (p.Pro1060=)
c.3081T>A (p.Pro1027=)
c.3495T>A (p.Pro1165=)
16g.9764205_9764213delinsAGGGGAGCTCA2206693111GRIN2Ac.3331_3339delinsAGCTCCCCT (p.Ser1111=)
c.2860_2868delinsAGCTCCCCT (p.Ser954=)
n.2924_2932delinsAGCTCCCCT
c.*701_*709delinsAGCTCCCCT (n.*701_*709delinsAGCTCCCCT)
c.2920_2928delinsAGCTCCCCT (p.Ser974=)
n.2970_2978delinsAGCTCCCCT
c.3172_3180delinsAGCTCCCCT (p.Ser1058=)
c.3073_3081delinsAGCTCCCCT (p.Ser1025=)
c.3487_3495delinsAGCTCCCCT (p.Ser1163=)
16g.9764206G>ACA7896334GRIN2Ac.3338C>T (p.Pro1113Leu)
c.2867C>T (p.Pro956Leu)
n.2931C>T
c.*708C>T (n.*708C>T)
c.2927C>T (p.Pro976Leu)
n.2977C>T
c.3179C>T (p.Pro1060Leu)
c.3080C>T (p.Pro1027Leu)
c.3494C>T (p.Pro1165Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.9764206G>CCA394708084GRIN2Ac.3338C>G (p.Pro1113Arg)
c.2867C>G (p.Pro956Arg)
n.2931C>G
c.*708C>G (n.*708C>G)
c.2927C>G (p.Pro976Arg)
n.2977C>G
c.3179C>G (p.Pro1060Arg)
c.3080C>G (p.Pro1027Arg)
c.3494C>G (p.Pro1165Arg)
 dbSNP
16g.9764206G=CA2206693112GRIN2Ac.3338C= (p.Pro1113=)
c.2867C= (p.Pro956=)
n.2931C=
c.*708C= (n.*708C=)
c.2927C= (p.Pro976=)
n.2977C=
c.3179C= (p.Pro1060=)
c.3080C= (p.Pro1027=)
c.3494C= (p.Pro1165=)
16g.9764206G>TCA394708085GRIN2Ac.3338C>A (p.Pro1113His)
c.2867C>A (p.Pro956His)
n.2931C>A
c.*708C>A (n.*708C>A)
c.2927C>A (p.Pro976His)
n.2977C>A
c.3179C>A (p.Pro1060His)
c.3080C>A (p.Pro1027His)
c.3494C>A (p.Pro1165His)
 dbSNP
16g.9764206_9764212delCA974532284GRIN2Ac.3332_3338del (p.Ser1111IlefsTer8)
c.2861_2867del (p.Ser954IlefsTer8)
n.2925_2931del
c.*702_*708del (n.*702_*708del)
c.2921_2927del (p.Ser974IlefsTer8)
n.2971_2977del
c.3173_3179del (p.Ser1058IlefsTer8)
c.3074_3080del (p.Ser1025IlefsTer8)
c.3488_3494del (p.Ser1163IlefsTer8)
 gnomAD v3 gnomAD v4
16g.9764206_9764213delCA621175132GRIN2Ac.3331_3338del (p.Ser1111Ter)
c.2860_2867del (p.Ser954Ter)
n.2924_2931del
c.*701_*708del (n.*701_*708del)
c.2920_2927del (p.Ser974Ter)
n.2970_2977del
c.3172_3179del (p.Ser1058Ter)
c.3073_3080del (p.Ser1025Ter)
c.3487_3494del (p.Ser1163Ter)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.9764206_9764207insTCA974532289GRIN2Ac.3337_3338insA (p.Pro1113HisfsTer2)
c.2866_2867insA (p.Pro956HisfsTer2)
n.2930_2931insA
c.*707_*708insA (n.*707_*708insA)
c.2926_2927insA (p.Pro976HisfsTer2)
n.2976_2977insA
c.3178_3179insA (p.Pro1060HisfsTer2)
c.3079_3080insA (p.Pro1027HisfsTer2)
c.3493_3494insA (p.Pro1165HisfsTer2)
 gnomAD v3 gnomAD v4
16g.9764207G>ACA394708086GRIN2Ac.3337C>T (p.Pro1113Ser)
c.2866C>T (p.Pro956Ser)
n.2930C>T
c.*707C>T (n.*707C>T)
c.2926C>T (p.Pro976Ser)
n.2976C>T
c.3178C>T (p.Pro1060Ser)
c.3079C>T (p.Pro1027Ser)
c.3493C>T (p.Pro1165Ser)
 dbSNP
16g.9764207G>CCA394708087GRIN2Ac.3337C>G (p.Pro1113Ala)
c.2866C>G (p.Pro956Ala)
n.2930C>G
c.*707C>G (n.*707C>G)
c.2926C>G (p.Pro976Ala)
n.2976C>G
c.3178C>G (p.Pro1060Ala)
c.3079C>G (p.Pro1027Ala)
c.3493C>G (p.Pro1165Ala)
 dbSNP gnomAD v3 gnomAD v4
16g.9764207G=CA2206693114GRIN2Ac.3337C= (p.Pro1113=)
c.2866C= (p.Pro956=)
n.2930C=
c.*707C= (n.*707C=)
c.2926C= (p.Pro976=)
n.2976C=
c.3178C= (p.Pro1060=)
c.3079C= (p.Pro1027=)
c.3493C= (p.Pro1165=)
16g.9764207G>TCA394708088GRIN2Ac.3337C>A (p.Pro1113Thr)
c.2866C>A (p.Pro956Thr)
n.2930C>A
c.*707C>A (n.*707C>A)
c.2926C>A (p.Pro976Thr)
n.2976C>A
c.3178C>A (p.Pro1060Thr)
c.3079C>A (p.Pro1027Thr)
c.3493C>A (p.Pro1165Thr)
 dbSNP
16g.9764207_9764208delinsAACA645570190GRIN2Ac.3336_3337delinsTT (p.Pro1113Ser)
c.2865_2866delinsTT (p.Pro956Ser)
n.2929_2930delinsTT
c.*706_*707delinsTT (n.*706_*707delinsTT)
c.2925_2926delinsTT (p.Pro976Ser)
n.2975_2976delinsTT
c.3177_3178delinsTT (p.Pro1060Ser)
c.3078_3079delinsTT (p.Pro1027Ser)
c.3492_3493delinsTT (p.Pro1165Ser)
 COSMIC
16g.9764207_9764218delinsGGGAGCTTGATTCA2206693113GRIN2Ac.3326_3337delinsAATCAAGCTCCC (p.Lys1109=)
c.2855_2866delinsAATCAAGCTCCC (p.Lys952=)
n.2919_2930delinsAATCAAGCTCCC
c.*696_*707delinsAATCAAGCTCCC (n.*696_*707delinsAATCAAGCTCCC)
c.2915_2926delinsAATCAAGCTCCC (p.Lys972=)
n.2965_2976delinsAATCAAGCTCCC
c.3167_3178delinsAATCAAGCTCCC (p.Lys1056=)
c.3068_3079delinsAATCAAGCTCCC (p.Lys1023=)
c.3482_3493delinsAATCAAGCTCCC (p.Lys1161=)
16g.9764207_9764208insCCCA974532298GRIN2Ac.3336_3337insGG (p.Pro1113GlyfsTer9)
c.2865_2866insGG (p.Pro956GlyfsTer9)
n.2929_2930insGG
c.*706_*707insGG (n.*706_*707insGG)
c.2925_2926insGG (p.Pro976GlyfsTer9)
n.2975_2976insGG
c.3177_3178insGG (p.Pro1060GlyfsTer9)
c.3078_3079insGG (p.Pro1027GlyfsTer9)
c.3492_3493insGG (p.Pro1165GlyfsTer9)
 gnomAD v3 gnomAD v4
16g.9764207_9764208insTCCA974532322GRIN2Ac.3336_3337insGA (p.Pro1113AspfsTer9)
c.2865_2866insGA (p.Pro956AspfsTer9)
n.2929_2930insGA
c.*706_*707insGA (n.*706_*707insGA)
c.2925_2926insGA (p.Pro976AspfsTer9)
n.2975_2976insGA
c.3177_3178insGA (p.Pro1060AspfsTer9)
c.3078_3079insGA (p.Pro1027AspfsTer9)
c.3492_3493insGA (p.Pro1165AspfsTer9)
 gnomAD v3 gnomAD v4
16g.9764208G>ACA493692998GRIN2Ac.3336C>T (p.Ser1112=)
c.2865C>T (p.Ser955=)
n.2929C>T
c.*706C>T (n.*706C>T)
c.2925C>T (p.Ser975=)
n.2975C>T
c.3177C>T (p.Ser1059=)
c.3078C>T (p.Ser1026=)
c.3492C>T (p.Ser1164=)
 dbSNP gnomAD v4
16g.9764208G>CCA493692999GRIN2Ac.3336C>G (p.Ser1112=)
c.2865C>G (p.Ser955=)
n.2929C>G
c.*706C>G (n.*706C>G)
c.2925C>G (p.Ser975=)
n.2975C>G
c.3177C>G (p.Ser1059=)
c.3078C>G (p.Ser1026=)
c.3492C>G (p.Ser1164=)
 gnomAD v3 gnomAD v4
16g.9764208G>TCA493693000GRIN2Ac.3336C>A (p.Ser1112=)
c.2865C>A (p.Ser955=)
n.2929C>A
c.*706C>A (n.*706C>A)
c.2925C>A (p.Ser975=)
n.2975C>A
c.3177C>A (p.Ser1059=)
c.3078C>A (p.Ser1026=)
c.3492C>A (p.Ser1164=)
 COSMIC
16g.9764208_9764218delCA621175133GRIN2Ac.3326_3336del (p.Lys1109ThrfsTer2)
c.2855_2865del (p.Lys952ThrfsTer2)
n.2919_2929del
c.*696_*706del (n.*696_*706del)
c.2915_2925del (p.Lys972ThrfsTer2)
n.2965_2975del
c.3167_3177del (p.Lys1056ThrfsTer2)
c.3068_3078del (p.Lys1023ThrfsTer2)
c.3482_3492del (p.Lys1161ThrfsTer2)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched