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.9764004G>ACA493693270GRIN2Ac.3540C>T (p.Asn1180=)
c.3069C>T (p.Asn1023=)
n.3133C>T
c.*910C>T (n.*910C>T)
c.3129C>T (p.Asn1043=)
n.3179C>T
c.3381C>T (p.Asn1127=)
c.3282C>T (p.Asn1094=)
c.3696C>T (p.Asn1232=)
16g.9764004G>CCA394707404GRIN2Ac.3540C>G (p.Asn1180Lys)
c.3069C>G (p.Asn1023Lys)
n.3133C>G
c.*910C>G (n.*910C>G)
c.3129C>G (p.Asn1043Lys)
n.3179C>G
c.3381C>G (p.Asn1127Lys)
c.3282C>G (p.Asn1094Lys)
c.3696C>G (p.Asn1232Lys)
 dbSNP
16g.9764004G>TCA394707405GRIN2Ac.3540C>A (p.Asn1180Lys)
c.3069C>A (p.Asn1023Lys)
n.3133C>A
c.*910C>A (n.*910C>A)
c.3129C>A (p.Asn1043Lys)
n.3179C>A
c.3381C>A (p.Asn1127Lys)
c.3282C>A (p.Asn1094Lys)
c.3696C>A (p.Asn1232Lys)
16g.9764005T>ACA394707406GRIN2Ac.3539A>T (p.Asn1180Ile)
c.3068A>T (p.Asn1023Ile)
n.3132A>T
c.*909A>T (n.*909A>T)
c.3128A>T (p.Asn1043Ile)
n.3178A>T
c.3380A>T (p.Asn1127Ile)
c.3281A>T (p.Asn1094Ile)
c.3695A>T (p.Asn1232Ile)
 ClinVar dbSNP gnomAD v3 gnomAD v4
16g.9764005T>CCA277537043GRIN2Ac.3539A>G (p.Asn1180Ser)
c.3068A>G (p.Asn1023Ser)
n.3132A>G
c.*909A>G (n.*909A>G)
c.3128A>G (p.Asn1043Ser)
n.3178A>G
c.3380A>G (p.Asn1127Ser)
c.3281A>G (p.Asn1094Ser)
c.3695A>G (p.Asn1232Ser)
 dbSNP gnomAD v3 gnomAD v4
16g.9764005T>GCA394707407GRIN2Ac.3539A>C (p.Asn1180Thr)
c.3068A>C (p.Asn1023Thr)
n.3132A>C
c.*909A>C (n.*909A>C)
c.3128A>C (p.Asn1043Thr)
n.3178A>C
c.3380A>C (p.Asn1127Thr)
c.3281A>C (p.Asn1094Thr)
c.3695A>C (p.Asn1232Thr)
 dbSNP
16g.9764005T=CA2206693005GRIN2Ac.3539A= (p.Asn1180=)
c.3068A= (p.Asn1023=)
n.3132A=
c.*909A= (n.*909A=)
c.3128A= (p.Asn1043=)
n.3178A=
c.3380A= (p.Asn1127=)
c.3281A= (p.Asn1094=)
c.3695A= (p.Asn1232=)
16g.9764006T>ACA394707408GRIN2Ac.3538A>T (p.Asn1180Tyr)
c.3067A>T (p.Asn1023Tyr)
n.3131A>T
c.*908A>T (n.*908A>T)
c.3127A>T (p.Asn1043Tyr)
n.3177A>T
c.3379A>T (p.Asn1127Tyr)
c.3280A>T (p.Asn1094Tyr)
c.3694A>T (p.Asn1232Tyr)
 dbSNP
16g.9764006T>CCA277537053GRIN2Ac.3538A>G (p.Asn1180Asp)
c.3067A>G (p.Asn1023Asp)
n.3131A>G
c.*908A>G (n.*908A>G)
c.3127A>G (p.Asn1043Asp)
n.3177A>G
c.3379A>G (p.Asn1127Asp)
c.3280A>G (p.Asn1094Asp)
c.3694A>G (p.Asn1232Asp)
 dbSNP gnomAD v3 gnomAD v4
16g.9764006T>GCA394707409GRIN2Ac.3538A>C (p.Asn1180His)
c.3067A>C (p.Asn1023His)
n.3131A>C
c.*908A>C (n.*908A>C)
c.3127A>C (p.Asn1043His)
n.3177A>C
c.3379A>C (p.Asn1127His)
c.3280A>C (p.Asn1094His)
c.3694A>C (p.Asn1232His)
 dbSNP
16g.9764006T=CA2206693006GRIN2Ac.3538A= (p.Asn1180=)
c.3067A= (p.Asn1023=)
n.3131A=
c.*908A= (n.*908A=)
c.3127A= (p.Asn1043=)
n.3177A=
c.3379A= (p.Asn1127=)
c.3280A= (p.Asn1094=)
c.3694A= (p.Asn1232=)
16g.9764007G>ACA493693275GRIN2Ac.3537C>T (p.Ser1179=)
c.3066C>T (p.Ser1022=)
n.3130C>T
c.*907C>T (n.*907C>T)
c.3126C>T (p.Ser1042=)
n.3176C>T
c.3378C>T (p.Ser1126=)
c.3279C>T (p.Ser1093=)
c.3693C>T (p.Ser1231=)
 dbSNP COSMIC
16g.9764007G>CCA493693277GRIN2Ac.3537C>G (p.Ser1179=)
c.3066C>G (p.Ser1022=)
n.3130C>G
c.*907C>G (n.*907C>G)
c.3126C>G (p.Ser1042=)
n.3176C>G
c.3378C>G (p.Ser1126=)
c.3279C>G (p.Ser1093=)
c.3693C>G (p.Ser1231=)
16g.9764007G>TCA493693278GRIN2Ac.3537C>A (p.Ser1179=)
c.3066C>A (p.Ser1022=)
n.3130C>A
c.*907C>A (n.*907C>A)
c.3126C>A (p.Ser1042=)
n.3176C>A
c.3378C>A (p.Ser1126=)
c.3279C>A (p.Ser1093=)
c.3693C>A (p.Ser1231=)
 dbSNP
16g.9764008G>ACA394707410GRIN2Ac.3536C>T (p.Ser1179Phe)
c.3065C>T (p.Ser1022Phe)
n.3129C>T
c.*906C>T (n.*906C>T)
c.3125C>T (p.Ser1042Phe)
n.3175C>T
c.3377C>T (p.Ser1126Phe)
c.3278C>T (p.Ser1093Phe)
c.3692C>T (p.Ser1231Phe)
 dbSNP
16g.9764008G>CCA394707411GRIN2Ac.3536C>G (p.Ser1179Cys)
c.3065C>G (p.Ser1022Cys)
n.3129C>G
c.*906C>G (n.*906C>G)
c.3125C>G (p.Ser1042Cys)
n.3175C>G
c.3377C>G (p.Ser1126Cys)
c.3278C>G (p.Ser1093Cys)
c.3692C>G (p.Ser1231Cys)
 dbSNP
16g.9764008G=CA2206693007GRIN2Ac.3536C= (p.Ser1179=)
c.3065C= (p.Ser1022=)
n.3129C=
c.*906C= (n.*906C=)
c.3125C= (p.Ser1042=)
n.3175C=
c.3377C= (p.Ser1126=)
c.3278C= (p.Ser1093=)
c.3692C= (p.Ser1231=)
16g.9764008G>TCA7896294GRIN2Ac.3536C>A (p.Ser1179Tyr)
c.3065C>A (p.Ser1022Tyr)
n.3129C>A
c.*906C>A (n.*906C>A)
c.3125C>A (p.Ser1042Tyr)
n.3175C>A
c.3377C>A (p.Ser1126Tyr)
c.3278C>A (p.Ser1093Tyr)
c.3692C>A (p.Ser1231Tyr)
 dbSNP ExAC gnomAD v2
16g.9764009A=CA2206693008GRIN2Ac.3535T= (p.Ser1179=)
c.3064T= (p.Ser1022=)
n.3128T=
c.*905T= (n.*905T=)
c.3124T= (p.Ser1042=)
n.3174T=
c.3376T= (p.Ser1126=)
c.3277T= (p.Ser1093=)
c.3691T= (p.Ser1231=)
16g.9764009A>CCA7896295GRIN2Ac.3535T>G (p.Ser1179Ala)
c.3064T>G (p.Ser1022Ala)
n.3128T>G
c.*905T>G (n.*905T>G)
c.3124T>G (p.Ser1042Ala)
n.3174T>G
c.3376T>G (p.Ser1126Ala)
c.3277T>G (p.Ser1093Ala)
c.3691T>G (p.Ser1231Ala)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.9764009A>GCA394707413GRIN2Ac.3535T>C (p.Ser1179Pro)
c.3064T>C (p.Ser1022Pro)
n.3128T>C
c.*905T>C (n.*905T>C)
c.3124T>C (p.Ser1042Pro)
n.3174T>C
c.3376T>C (p.Ser1126Pro)
c.3277T>C (p.Ser1093Pro)
c.3691T>C (p.Ser1231Pro)
 dbSNP gnomAD v4
16g.9764009A>TCA394707412GRIN2Ac.3535T>A (p.Ser1179Thr)
c.3064T>A (p.Ser1022Thr)
n.3128T>A
c.*905T>A (n.*905T>A)
c.3124T>A (p.Ser1042Thr)
n.3174T>A
c.3376T>A (p.Ser1126Thr)
c.3277T>A (p.Ser1093Thr)
c.3691T>A (p.Ser1231Thr)
 dbSNP
16g.9764010A>CCA493693293GRIN2Ac.3534T>G (p.Leu1178=)
c.3063T>G (p.Leu1021=)
n.3127T>G
c.*904T>G (n.*904T>G)
c.3123T>G (p.Leu1041=)
n.3173T>G
c.3375T>G (p.Leu1125=)
c.3276T>G (p.Leu1092=)
c.3690T>G (p.Leu1230=)
 COSMIC
16g.9764010A>GCA493693287GRIN2Ac.3534T>C (p.Leu1178=)
c.3063T>C (p.Leu1021=)
n.3127T>C
c.*904T>C (n.*904T>C)
c.3123T>C (p.Leu1041=)
n.3173T>C
c.3375T>C (p.Leu1125=)
c.3276T>C (p.Leu1092=)
c.3690T>C (p.Leu1230=)
 dbSNP
16g.9764010A>TCA493693289GRIN2Ac.3534T>A (p.Leu1178=)
c.3063T>A (p.Leu1021=)
n.3127T>A
c.*904T>A (n.*904T>A)
c.3123T>A (p.Leu1041=)
n.3173T>A
c.3375T>A (p.Leu1125=)
c.3276T>A (p.Leu1092=)
c.3690T>A (p.Leu1230=)
 dbSNP
16g.9764011A>CCA394707414GRIN2Ac.3533T>G (p.Leu1178Arg)
c.3062T>G (p.Leu1021Arg)
n.3126T>G
c.*903T>G (n.*903T>G)
c.3122T>G (p.Leu1041Arg)
n.3172T>G
c.3374T>G (p.Leu1125Arg)
c.3275T>G (p.Leu1092Arg)
c.3689T>G (p.Leu1230Arg)
 dbSNP
16g.9764011A>GCA394707415GRIN2Ac.3533T>C (p.Leu1178Pro)
c.3062T>C (p.Leu1021Pro)
n.3126T>C
c.*903T>C (n.*903T>C)
c.3122T>C (p.Leu1041Pro)
n.3172T>C
c.3374T>C (p.Leu1125Pro)
c.3275T>C (p.Leu1092Pro)
c.3689T>C (p.Leu1230Pro)
 dbSNP
16g.9764011A>TCA394707416GRIN2Ac.3533T>A (p.Leu1178His)
c.3062T>A (p.Leu1021His)
n.3126T>A
c.*903T>A (n.*903T>A)
c.3122T>A (p.Leu1041His)
n.3172T>A
c.3374T>A (p.Leu1125His)
c.3275T>A (p.Leu1092His)
c.3689T>A (p.Leu1230His)
 dbSNP
16g.9764012G>ACA394707417GRIN2Ac.3532C>T (p.Leu1178Phe)
c.3061C>T (p.Leu1021Phe)
n.3125C>T
c.*902C>T (n.*902C>T)
c.3121C>T (p.Leu1041Phe)
n.3171C>T
c.3373C>T (p.Leu1125Phe)
c.3274C>T (p.Leu1092Phe)
c.3688C>T (p.Leu1230Phe)
 gnomAD v4
16g.9764012G>CCA394707418GRIN2Ac.3532C>G (p.Leu1178Val)
c.3061C>G (p.Leu1021Val)
n.3125C>G
c.*902C>G (n.*902C>G)
c.3121C>G (p.Leu1041Val)
n.3171C>G
c.3373C>G (p.Leu1125Val)
c.3274C>G (p.Leu1092Val)
c.3688C>G (p.Leu1230Val)
16g.9764012G=CA2206693009GRIN2Ac.3532C= (p.Leu1178=)
c.3061C= (p.Leu1021=)
n.3125C=
c.*902C= (n.*902C=)
c.3121C= (p.Leu1041=)
n.3171C=
c.3373C= (p.Leu1125=)
c.3274C= (p.Leu1092=)
c.3688C= (p.Leu1230=)
16g.9764012G>TCA7896296GRIN2Ac.3532C>A (p.Leu1178Ile)
c.3061C>A (p.Leu1021Ile)
n.3125C>A
c.*902C>A (n.*902C>A)
c.3121C>A (p.Leu1041Ile)
n.3171C>A
c.3373C>A (p.Leu1125Ile)
c.3274C>A (p.Leu1092Ile)
c.3688C>A (p.Leu1230Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.9764013C>ACA277537103GRIN2Ac.3531G>T (p.Gly1177=)
c.3060G>T (p.Gly1020=)
n.3124G>T
c.*901G>T (n.*901G>T)
c.3120G>T (p.Gly1040=)
n.3170G>T
c.3372G>T (p.Gly1124=)
c.3273G>T (p.Gly1091=)
c.3687G>T (p.Gly1229=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.9764013C=CA2206693010GRIN2Ac.3531G= (p.Gly1177=)
c.3060G= (p.Gly1020=)
n.3124G=
c.*901G= (n.*901G=)
c.3120G= (p.Gly1040=)
n.3170G=
c.3372G= (p.Gly1124=)
c.3273G= (p.Gly1091=)
c.3687G= (p.Gly1229=)
16g.9764013C>GCA493693301GRIN2Ac.3531G>C (p.Gly1177=)
c.3060G>C (p.Gly1020=)
n.3124G>C
c.*901G>C (n.*901G>C)
c.3120G>C (p.Gly1040=)
n.3170G>C
c.3372G>C (p.Gly1124=)
c.3273G>C (p.Gly1091=)
c.3687G>C (p.Gly1229=)
 dbSNP
16g.9764013C>TCA493693302GRIN2Ac.3531G>A (p.Gly1177=)
c.3060G>A (p.Gly1020=)
n.3124G>A
c.*901G>A (n.*901G>A)
c.3120G>A (p.Gly1040=)
n.3170G>A
c.3372G>A (p.Gly1124=)
c.3273G>A (p.Gly1091=)
c.3687G>A (p.Gly1229=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
16g.9764014C>ACA394707419GRIN2Ac.3530G>T (p.Gly1177Val)
c.3059G>T (p.Gly1020Val)
n.3123G>T
c.*900G>T (n.*900G>T)
c.3119G>T (p.Gly1040Val)
n.3169G>T
c.3371G>T (p.Gly1124Val)
c.3272G>T (p.Gly1091Val)
c.3686G>T (p.Gly1229Val)
16g.9764014C=CA2206693011GRIN2Ac.3530G= (p.Gly1177=)
c.3059G= (p.Gly1020=)
n.3123G=
c.*900G= (n.*900G=)
c.3119G= (p.Gly1040=)
n.3169G=
c.3371G= (p.Gly1124=)
c.3272G= (p.Gly1091=)
c.3686G= (p.Gly1229=)
16g.9764014C>GCA394707420GRIN2Ac.3530G>C (p.Gly1177Ala)
c.3059G>C (p.Gly1020Ala)
n.3123G>C
c.*900G>C (n.*900G>C)
c.3119G>C (p.Gly1040Ala)
n.3169G>C
c.3371G>C (p.Gly1124Ala)
c.3272G>C (p.Gly1091Ala)
c.3686G>C (p.Gly1229Ala)
 dbSNP
16g.9764014C>TCA7896297GRIN2Ac.3530G>A (p.Gly1177Glu)
c.3059G>A (p.Gly1020Glu)
n.3123G>A
c.*900G>A (n.*900G>A)
c.3119G>A (p.Gly1040Glu)
n.3169G>A
c.3371G>A (p.Gly1124Glu)
c.3272G>A (p.Gly1091Glu)
c.3686G>A (p.Gly1229Glu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.9764015C>ACA394707421GRIN2Ac.3529G>T (p.Gly1177Trp)
c.3058G>T (p.Gly1020Trp)
n.3122G>T
c.*899G>T (n.*899G>T)
c.3118G>T (p.Gly1040Trp)
n.3168G>T
c.3370G>T (p.Gly1124Trp)
c.3271G>T (p.Gly1091Trp)
c.3685G>T (p.Gly1229Trp)
16g.9764015C>GCA394707422GRIN2Ac.3529G>C (p.Gly1177Arg)
c.3058G>C (p.Gly1020Arg)
n.3122G>C
c.*899G>C (n.*899G>C)
c.3118G>C (p.Gly1040Arg)
n.3168G>C
c.3370G>C (p.Gly1124Arg)
c.3271G>C (p.Gly1091Arg)
c.3685G>C (p.Gly1229Arg)
 dbSNP
16g.9764015C>TCA394707423GRIN2Ac.3529G>A (p.Gly1177Arg)
c.3058G>A (p.Gly1020Arg)
n.3122G>A
c.*899G>A (n.*899G>A)
c.3118G>A (p.Gly1040Arg)
n.3168G>A
c.3370G>A (p.Gly1124Arg)
c.3271G>A (p.Gly1091Arg)
c.3685G>A (p.Gly1229Arg)
 COSMIC
16g.9764016C>ACA394707424GRIN2Ac.3528G>T (p.Glu1176Asp)
c.3057G>T (p.Glu1019Asp)
n.3121G>T
c.*898G>T (n.*898G>T)
c.3117G>T (p.Glu1039Asp)
n.3167G>T
c.3369G>T (p.Glu1123Asp)
c.3270G>T (p.Glu1090Asp)
c.3684G>T (p.Glu1228Asp)
 dbSNP
16g.9764016C>GCA394707425GRIN2Ac.3528G>C (p.Glu1176Asp)
c.3057G>C (p.Glu1019Asp)
n.3121G>C
c.*898G>C (n.*898G>C)
c.3117G>C (p.Glu1039Asp)
n.3167G>C
c.3369G>C (p.Glu1123Asp)
c.3270G>C (p.Glu1090Asp)
c.3684G>C (p.Glu1228Asp)
16g.9764016C>TCA493693312GRIN2Ac.3528G>A (p.Glu1176=)
c.3057G>A (p.Glu1019=)
n.3121G>A
c.*898G>A (n.*898G>A)
c.3117G>A (p.Glu1039=)
n.3167G>A
c.3369G>A (p.Glu1123=)
c.3270G>A (p.Glu1090=)
c.3684G>A (p.Glu1228=)
 dbSNP gnomAD v4
16g.9764017T>ACA394707426GRIN2Ac.3527A>T (p.Glu1176Val)
c.3056A>T (p.Glu1019Val)
n.3120A>T
c.*897A>T (n.*897A>T)
c.3116A>T (p.Glu1039Val)
n.3166A>T
c.3368A>T (p.Glu1123Val)
c.3269A>T (p.Glu1090Val)
c.3683A>T (p.Glu1228Val)
 dbSNP
16g.9764017T>CCA394707427GRIN2Ac.3527A>G (p.Glu1176Gly)
c.3056A>G (p.Glu1019Gly)
n.3120A>G
c.*897A>G (n.*897A>G)
c.3116A>G (p.Glu1039Gly)
n.3166A>G
c.3368A>G (p.Glu1123Gly)
c.3269A>G (p.Glu1090Gly)
c.3683A>G (p.Glu1228Gly)
 dbSNP
16g.9764017T>GCA394707428GRIN2Ac.3527A>C (p.Glu1176Ala)
c.3056A>C (p.Glu1019Ala)
n.3120A>C
c.*897A>C (n.*897A>C)
c.3116A>C (p.Glu1039Ala)
n.3166A>C
c.3368A>C (p.Glu1123Ala)
c.3269A>C (p.Glu1090Ala)
c.3683A>C (p.Glu1228Ala)
16g.9764018C>ACA394707429GRIN2Ac.3526G>T (p.Glu1176Ter)
c.3055G>T (p.Glu1019Ter)
n.3119G>T
c.*896G>T (n.*896G>T)
c.3115G>T (p.Glu1039Ter)
n.3165G>T
c.3367G>T (p.Glu1123Ter)
c.3268G>T (p.Glu1090Ter)
c.3682G>T (p.Glu1228Ter)
 dbSNP COSMIC
16g.9764018C=CA2206693012GRIN2Ac.3526G= (p.Glu1176=)
c.3055G= (p.Glu1019=)
n.3119G=
c.*896G= (n.*896G=)
c.3115G= (p.Glu1039=)
n.3165G=
c.3367G= (p.Glu1123=)
c.3268G= (p.Glu1090=)
c.3682G= (p.Glu1228=)
16g.9764018C>GCA394707430GRIN2Ac.3526G>C (p.Glu1176Gln)
c.3055G>C (p.Glu1019Gln)
n.3119G>C
c.*896G>C (n.*896G>C)
c.3115G>C (p.Glu1039Gln)
n.3165G>C
c.3367G>C (p.Glu1123Gln)
c.3268G>C (p.Glu1090Gln)
c.3682G>C (p.Glu1228Gln)
 ClinVar dbSNP gnomAD v4
16g.9764018C>TCA394707431GRIN2Ac.3526G>A (p.Glu1176Lys)
c.3055G>A (p.Glu1019Lys)
n.3119G>A
c.*896G>A (n.*896G>A)
c.3115G>A (p.Glu1039Lys)
n.3165G>A
c.3367G>A (p.Glu1123Lys)
c.3268G>A (p.Glu1090Lys)
c.3682G>A (p.Glu1228Lys)
 dbSNP gnomAD v4
16g.9764019T>ACA394707432GRIN2Ac.3525A>T (p.Glu1175Asp)
c.3054A>T (p.Glu1018Asp)
n.3118A>T
c.*895A>T (n.*895A>T)
c.3114A>T (p.Glu1038Asp)
n.3164A>T
c.3366A>T (p.Glu1122Asp)
c.3267A>T (p.Glu1089Asp)
c.3681A>T (p.Glu1227Asp)
 ClinVar dbSNP
16g.9764019T>CCA493693327GRIN2Ac.3525A>G (p.Glu1175=)
c.3054A>G (p.Glu1018=)
n.3118A>G
c.*895A>G (n.*895A>G)
c.3114A>G (p.Glu1038=)
n.3164A>G
c.3366A>G (p.Glu1122=)
c.3267A>G (p.Glu1089=)
c.3681A>G (p.Glu1227=)
 dbSNP
16g.9764019T>GCA394707433GRIN2Ac.3525A>C (p.Glu1175Asp)
c.3054A>C (p.Glu1018Asp)
n.3118A>C
c.*895A>C (n.*895A>C)
c.3114A>C (p.Glu1038Asp)
n.3164A>C
c.3366A>C (p.Glu1122Asp)
c.3267A>C (p.Glu1089Asp)
c.3681A>C (p.Glu1227Asp)
16g.9764019T=CA2206693013GRIN2Ac.3525A= (p.Glu1175=)
c.3054A= (p.Glu1018=)
n.3118A=
c.*895A= (n.*895A=)
c.3114A= (p.Glu1038=)
n.3164A=
c.3366A= (p.Glu1122=)
c.3267A= (p.Glu1089=)
c.3681A= (p.Glu1227=)
16g.9764020T>ACA394707434GRIN2Ac.3524A>T (p.Glu1175Val)
c.3053A>T (p.Glu1018Val)
n.3117A>T
c.*894A>T (n.*894A>T)
c.3113A>T (p.Glu1038Val)
n.3163A>T
c.3365A>T (p.Glu1122Val)
c.3266A>T (p.Glu1089Val)
c.3680A>T (p.Glu1227Val)
 dbSNP
16g.9764020T>CCA394707435GRIN2Ac.3524A>G (p.Glu1175Gly)
c.3053A>G (p.Glu1018Gly)
n.3117A>G
c.*894A>G (n.*894A>G)
c.3113A>G (p.Glu1038Gly)
n.3163A>G
c.3365A>G (p.Glu1122Gly)
c.3266A>G (p.Glu1089Gly)
c.3680A>G (p.Glu1227Gly)
16g.9764020T>GCA394707436GRIN2Ac.3524A>C (p.Glu1175Ala)
c.3053A>C (p.Glu1018Ala)
n.3117A>C
c.*894A>C (n.*894A>C)
c.3113A>C (p.Glu1038Ala)
n.3163A>C
c.3365A>C (p.Glu1122Ala)
c.3266A>C (p.Glu1089Ala)
c.3680A>C (p.Glu1227Ala)
16g.9764021C>ACA394707438GRIN2Ac.3523G>T (p.Glu1175Ter)
c.3052G>T (p.Glu1018Ter)
n.3116G>T
c.*893G>T (n.*893G>T)
c.3112G>T (p.Glu1038Ter)
n.3162G>T
c.3364G>T (p.Glu1122Ter)
c.3265G>T (p.Glu1089Ter)
c.3679G>T (p.Glu1227Ter)
 dbSNP
16g.9764021C=CA2206693014GRIN2Ac.3523G= (p.Glu1175=)
c.3052G= (p.Glu1018=)
n.3116G=
c.*893G= (n.*893G=)
c.3112G= (p.Glu1038=)
n.3162G=
c.3364G= (p.Glu1122=)
c.3265G= (p.Glu1089=)
c.3679G= (p.Glu1227=)
16g.9764021C>GCA394707437GRIN2Ac.3523G>C (p.Glu1175Gln)
c.3052G>C (p.Glu1018Gln)
n.3116G>C
c.*893G>C (n.*893G>C)
c.3112G>C (p.Glu1038Gln)
n.3162G>C
c.3364G>C (p.Glu1122Gln)
c.3265G>C (p.Glu1089Gln)
c.3679G>C (p.Glu1227Gln)
 dbSNP
16g.9764021C>TCA277537117GRIN2Ac.3523G>A (p.Glu1175Lys)
c.3052G>A (p.Glu1018Lys)
n.3116G>A
c.*893G>A (n.*893G>A)
c.3112G>A (p.Glu1038Lys)
n.3162G>A
c.3364G>A (p.Glu1122Lys)
c.3265G>A (p.Glu1089Lys)
c.3679G>A (p.Glu1227Lys)
 dbSNP COSMIC
16g.9764022A=CA2206693015GRIN2Ac.3522T= (p.Asn1174=)
c.3051T= (p.Asn1017=)
n.3115T=
c.*892T= (n.*892T=)
c.3111T= (p.Asn1037=)
n.3161T=
c.3363T= (p.Asn1121=)
c.3264T= (p.Asn1088=)
c.3678T= (p.Asn1226=)
16g.9764022A>CCA394707439GRIN2Ac.3522T>G (p.Asn1174Lys)
c.3051T>G (p.Asn1017Lys)
n.3115T>G
c.*892T>G (n.*892T>G)
c.3111T>G (p.Asn1037Lys)
n.3161T>G
c.3363T>G (p.Asn1121Lys)
c.3264T>G (p.Asn1088Lys)
c.3678T>G (p.Asn1226Lys)
16g.9764022A>GCA7896298GRIN2Ac.3522T>C (p.Asn1174=)
c.3051T>C (p.Asn1017=)
n.3115T>C
c.*892T>C (n.*892T>C)
c.3111T>C (p.Asn1037=)
n.3161T>C
c.3363T>C (p.Asn1121=)
c.3264T>C (p.Asn1088=)
c.3678T>C (p.Asn1226=)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.9764022A>TCA7896299GRIN2Ac.3522T>A (p.Asn1174Lys)
c.3051T>A (p.Asn1017Lys)
n.3115T>A
c.*892T>A (n.*892T>A)
c.3111T>A (p.Asn1037Lys)
n.3161T>A
c.3363T>A (p.Asn1121Lys)
c.3264T>A (p.Asn1088Lys)
c.3678T>A (p.Asn1226Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.9764023T>ACA394707440GRIN2Ac.3521A>T (p.Asn1174Ile)
c.3050A>T (p.Asn1017Ile)
n.3114A>T
c.*891A>T (n.*891A>T)
c.3110A>T (p.Asn1037Ile)
n.3160A>T
c.3362A>T (p.Asn1121Ile)
c.3263A>T (p.Asn1088Ile)
c.3677A>T (p.Asn1226Ile)
 dbSNP
16g.9764023T>CCA394707441GRIN2Ac.3521A>G (p.Asn1174Ser)
c.3050A>G (p.Asn1017Ser)
n.3114A>G
c.*891A>G (n.*891A>G)
c.3110A>G (p.Asn1037Ser)
n.3160A>G
c.3362A>G (p.Asn1121Ser)
c.3263A>G (p.Asn1088Ser)
c.3677A>G (p.Asn1226Ser)
16g.9764023T>GCA394707442GRIN2Ac.3521A>C (p.Asn1174Thr)
c.3050A>C (p.Asn1017Thr)
n.3114A>C
c.*891A>C (n.*891A>C)
c.3110A>C (p.Asn1037Thr)
n.3160A>C
c.3362A>C (p.Asn1121Thr)
c.3263A>C (p.Asn1088Thr)
c.3677A>C (p.Asn1226Thr)
16g.9764024T>ACA394707443GRIN2Ac.3520A>T (p.Asn1174Tyr)
c.3049A>T (p.Asn1017Tyr)
n.3113A>T
c.*890A>T (n.*890A>T)
c.3109A>T (p.Asn1037Tyr)
n.3159A>T
c.3361A>T (p.Asn1121Tyr)
c.3262A>T (p.Asn1088Tyr)
c.3676A>T (p.Asn1226Tyr)
 dbSNP
16g.9764024T>CCA394707444GRIN2Ac.3520A>G (p.Asn1174Asp)
c.3049A>G (p.Asn1017Asp)
n.3113A>G
c.*890A>G (n.*890A>G)
c.3109A>G (p.Asn1037Asp)
n.3159A>G
c.3361A>G (p.Asn1121Asp)
c.3262A>G (p.Asn1088Asp)
c.3676A>G (p.Asn1226Asp)
 dbSNP gnomAD v4
16g.9764024T>GCA394707445GRIN2Ac.3520A>C (p.Asn1174His)
c.3049A>C (p.Asn1017His)
n.3113A>C
c.*890A>C (n.*890A>C)
c.3109A>C (p.Asn1037His)
n.3159A>C
c.3361A>C (p.Asn1121His)
c.3262A>C (p.Asn1088His)
c.3676A>C (p.Asn1226His)
16g.9764025A=CA2206693016GRIN2Ac.3519T= (p.His1173=)
c.3048T= (p.His1016=)
n.3112T=
c.*889T= (n.*889T=)
c.3108T= (p.His1036=)
n.3158T=
c.3360T= (p.His1120=)
c.3261T= (p.His1087=)
c.3675T= (p.His1225=)
16g.9764025A>CCA394707446GRIN2Ac.3519T>G (p.His1173Gln)
c.3048T>G (p.His1016Gln)
n.3112T>G
c.*889T>G (n.*889T>G)
c.3108T>G (p.His1036Gln)
n.3158T>G
c.3360T>G (p.His1120Gln)
c.3261T>G (p.His1087Gln)
c.3675T>G (p.His1225Gln)
16g.9764025A>GCA493693336GRIN2Ac.3519T>C (p.His1173=)
c.3048T>C (p.His1016=)
n.3112T>C
c.*889T>C (n.*889T>C)
c.3108T>C (p.His1036=)
n.3158T>C
c.3360T>C (p.His1120=)
c.3261T>C (p.His1087=)
c.3675T>C (p.His1225=)
16g.9764025A>TCA394707447GRIN2Ac.3519T>A (p.His1173Gln)
c.3048T>A (p.His1016Gln)
n.3112T>A
c.*889T>A (n.*889T>A)
c.3108T>A (p.His1036Gln)
n.3158T>A
c.3360T>A (p.His1120Gln)
c.3261T>A (p.His1087Gln)
c.3675T>A (p.His1225Gln)
 dbSNP gnomAD v3 gnomAD v4
16g.9764026T>ACA394707448GRIN2Ac.3518A>T (p.His1173Leu)
c.3047A>T (p.His1016Leu)
n.3111A>T
c.*888A>T (n.*888A>T)
c.3107A>T (p.His1036Leu)
n.3157A>T
c.3359A>T (p.His1120Leu)
c.3260A>T (p.His1087Leu)
c.3674A>T (p.His1225Leu)
 dbSNP
16g.9764026T>CCA277537159GRIN2Ac.3518A>G (p.His1173Arg)
c.3047A>G (p.His1016Arg)
n.3111A>G
c.*888A>G (n.*888A>G)
c.3107A>G (p.His1036Arg)
n.3157A>G
c.3359A>G (p.His1120Arg)
c.3260A>G (p.His1087Arg)
c.3674A>G (p.His1225Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.9764026T>GCA394707449GRIN2Ac.3518A>C (p.His1173Pro)
c.3047A>C (p.His1016Pro)
n.3111A>C
c.*888A>C (n.*888A>C)
c.3107A>C (p.His1036Pro)
n.3157A>C
c.3359A>C (p.His1120Pro)
c.3260A>C (p.His1087Pro)
c.3674A>C (p.His1225Pro)
 dbSNP
16g.9764026T=CA2206693017GRIN2Ac.3518A= (p.His1173=)
c.3047A= (p.His1016=)
n.3111A=
c.*888A= (n.*888A=)
c.3107A= (p.His1036=)
n.3157A=
c.3359A= (p.His1120=)
c.3260A= (p.His1087=)
c.3674A= (p.His1225=)
16g.9764027G>ACA394707452GRIN2Ac.3517C>T (p.His1173Tyr)
c.3046C>T (p.His1016Tyr)
n.3110C>T
c.*887C>T (n.*887C>T)
c.3106C>T (p.His1036Tyr)
n.3156C>T
c.3358C>T (p.His1120Tyr)
c.3259C>T (p.His1087Tyr)
c.3673C>T (p.His1225Tyr)
 dbSNP
16g.9764027G>CCA394707451GRIN2Ac.3517C>G (p.His1173Asp)
c.3046C>G (p.His1016Asp)
n.3110C>G
c.*887C>G (n.*887C>G)
c.3106C>G (p.His1036Asp)
n.3156C>G
c.3358C>G (p.His1120Asp)
c.3259C>G (p.His1087Asp)
c.3673C>G (p.His1225Asp)
 dbSNP gnomAD v4
16g.9764027G>TCA394707450GRIN2Ac.3517C>A (p.His1173Asn)
c.3046C>A (p.His1016Asn)
n.3110C>A
c.*887C>A (n.*887C>A)
c.3106C>A (p.His1036Asn)
n.3156C>A
c.3358C>A (p.His1120Asn)
c.3259C>A (p.His1087Asn)
c.3673C>A (p.His1225Asn)
16g.9764028C>ACA7896300GRIN2Ac.3516G>T (p.Leu1172Phe)
c.3045G>T (p.Leu1015Phe)
n.3109G>T
c.*886G>T (n.*886G>T)
c.3105G>T (p.Leu1035Phe)
n.3155G>T
c.3357G>T (p.Leu1119Phe)
c.3258G>T (p.Leu1086Phe)
c.3672G>T (p.Leu1224Phe)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.9764028C=CA2206693018GRIN2Ac.3516G= (p.Leu1172=)
c.3045G= (p.Leu1015=)
n.3109G=
c.*886G= (n.*886G=)
c.3105G= (p.Leu1035=)
n.3155G=
c.3357G= (p.Leu1119=)
c.3258G= (p.Leu1086=)
c.3672G= (p.Leu1224=)
16g.9764028C>GCA394707453GRIN2Ac.3516G>C (p.Leu1172Phe)
c.3045G>C (p.Leu1015Phe)
n.3109G>C
c.*886G>C (n.*886G>C)
c.3105G>C (p.Leu1035Phe)
n.3155G>C
c.3357G>C (p.Leu1119Phe)
c.3258G>C (p.Leu1086Phe)
c.3672G>C (p.Leu1224Phe)
 dbSNP
16g.9764028C>TCA493693348GRIN2Ac.3516G>A (p.Leu1172=)
c.3045G>A (p.Leu1015=)
n.3109G>A
c.*886G>A (n.*886G>A)
c.3105G>A (p.Leu1035=)
n.3155G>A
c.3357G>A (p.Leu1119=)
c.3258G>A (p.Leu1086=)
c.3672G>A (p.Leu1224=)
 dbSNP
16g.9764029A=CA2206693019GRIN2Ac.3515T= (p.Leu1172=)
c.3044T= (p.Leu1015=)
n.3108T=
c.*885T= (n.*885T=)
c.3104T= (p.Leu1035=)
n.3154T=
c.3356T= (p.Leu1119=)
c.3257T= (p.Leu1086=)
c.3671T= (p.Leu1224=)
16g.9764029A>CCA394707454GRIN2Ac.3515T>G (p.Leu1172Trp)
c.3044T>G (p.Leu1015Trp)
n.3108T>G
c.*885T>G (n.*885T>G)
c.3104T>G (p.Leu1035Trp)
n.3154T>G
c.3356T>G (p.Leu1119Trp)
c.3257T>G (p.Leu1086Trp)
c.3671T>G (p.Leu1224Trp)
16g.9764029A>GCA394707455GRIN2Ac.3515T>C (p.Leu1172Ser)
c.3044T>C (p.Leu1015Ser)
n.3108T>C
c.*885T>C (n.*885T>C)
c.3104T>C (p.Leu1035Ser)
n.3154T>C
c.3356T>C (p.Leu1119Ser)
c.3257T>C (p.Leu1086Ser)
c.3671T>C (p.Leu1224Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v4
16g.9764029A>TCA394707456GRIN2Ac.3515T>A (p.Leu1172Ter)
c.3044T>A (p.Leu1015Ter)
n.3108T>A
c.*885T>A (n.*885T>A)
c.3104T>A (p.Leu1035Ter)
n.3154T>A
c.3356T>A (p.Leu1119Ter)
c.3257T>A (p.Leu1086Ter)
c.3671T>A (p.Leu1224Ter)
 dbSNP
16g.9764030A>CCA394707457GRIN2Ac.3514T>G (p.Leu1172Val)
c.3043T>G (p.Leu1015Val)
n.3107T>G
c.*884T>G (n.*884T>G)
c.3103T>G (p.Leu1035Val)
n.3153T>G
c.3355T>G (p.Leu1119Val)
c.3256T>G (p.Leu1086Val)
c.3670T>G (p.Leu1224Val)
16g.9764030A>GCA493693356GRIN2Ac.3514T>C (p.Leu1172=)
c.3043T>C (p.Leu1015=)
n.3107T>C
c.*884T>C (n.*884T>C)
c.3103T>C (p.Leu1035=)
n.3153T>C
c.3355T>C (p.Leu1119=)
c.3256T>C (p.Leu1086=)
c.3670T>C (p.Leu1224=)
 gnomAD v4
16g.9764030A>TCA394707458GRIN2Ac.3514T>A (p.Leu1172Met)
c.3043T>A (p.Leu1015Met)
n.3107T>A
c.*884T>A (n.*884T>A)
c.3103T>A (p.Leu1035Met)
n.3153T>A
c.3355T>A (p.Leu1119Met)
c.3256T>A (p.Leu1086Met)
c.3670T>A (p.Leu1224Met)
16g.9764030_9764031delCA2508563121GRIN2Ac.3513_3514del (p.Leu1172AlafsTer2)
c.3042_3043del (p.Leu1015AlafsTer2)
n.3106_3107del
c.*883_*884del (n.*883_*884del)
c.3102_3103del (p.Leu1035AlafsTer2)
n.3152_3153del
c.3354_3355del (p.Leu1119AlafsTer2)
c.3255_3256del (p.Leu1086AlafsTer2)
c.3669_3670del (p.Leu1224AlafsTer2)
16g.9764031G>ACA493693360GRIN2Ac.3513C>T (p.Pro1171=)
c.3042C>T (p.Pro1014=)
n.3106C>T
c.*883C>T (n.*883C>T)
c.3102C>T (p.Pro1034=)
n.3152C>T
c.3354C>T (p.Pro1118=)
c.3255C>T (p.Pro1085=)
c.3669C>T (p.Pro1223=)
 ClinVar dbSNP gnomAD v4
16g.9764031G>CCA493693362GRIN2Ac.3513C>G (p.Pro1171=)
c.3042C>G (p.Pro1014=)
n.3106C>G
c.*883C>G (n.*883C>G)
c.3102C>G (p.Pro1034=)
n.3152C>G
c.3354C>G (p.Pro1118=)
c.3255C>G (p.Pro1085=)
c.3669C>G (p.Pro1223=)
 dbSNP
16g.9764031G=CA2206693020GRIN2Ac.3513C= (p.Pro1171=)
c.3042C= (p.Pro1014=)
n.3106C=
c.*883C= (n.*883C=)
c.3102C= (p.Pro1034=)
n.3152C=
c.3354C= (p.Pro1118=)
c.3255C= (p.Pro1085=)
c.3669C= (p.Pro1223=)
16g.9764031G>TCA493693361GRIN2Ac.3513C>A (p.Pro1171=)
c.3042C>A (p.Pro1014=)
n.3106C>A
c.*883C>A (n.*883C>A)
c.3102C>A (p.Pro1034=)
n.3152C>A
c.3354C>A (p.Pro1118=)
c.3255C>A (p.Pro1085=)
c.3669C>A (p.Pro1223=)
 dbSNP
16g.9764032G>ACA394707459GRIN2Ac.3512C>T (p.Pro1171Leu)
c.3041C>T (p.Pro1014Leu)
n.3105C>T
c.*882C>T (n.*882C>T)
c.3101C>T (p.Pro1034Leu)
n.3151C>T
c.3353C>T (p.Pro1118Leu)
c.3254C>T (p.Pro1085Leu)
c.3668C>T (p.Pro1223Leu)
 COSMIC
16g.9764032G>CCA394707460GRIN2Ac.3512C>G (p.Pro1171Arg)
c.3041C>G (p.Pro1014Arg)
n.3105C>G
c.*882C>G (n.*882C>G)
c.3101C>G (p.Pro1034Arg)
n.3151C>G
c.3353C>G (p.Pro1118Arg)
c.3254C>G (p.Pro1085Arg)
c.3668C>G (p.Pro1223Arg)
16g.9764032G>TCA394707461GRIN2Ac.3512C>A (p.Pro1171His)
c.3041C>A (p.Pro1014His)
n.3105C>A
c.*882C>A (n.*882C>A)
c.3101C>A (p.Pro1034His)
n.3151C>A
c.3353C>A (p.Pro1118His)
c.3254C>A (p.Pro1085His)
c.3668C>A (p.Pro1223His)
16g.9764033G>ACA7896302GRIN2Ac.3511C>T (p.Pro1171Ser)
c.3040C>T (p.Pro1014Ser)
n.3104C>T
c.*881C>T (n.*881C>T)
c.3100C>T (p.Pro1034Ser)
n.3150C>T
c.3352C>T (p.Pro1118Ser)
c.3253C>T (p.Pro1085Ser)
c.3667C>T (p.Pro1223Ser)
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
16g.9764033G>CCA394707462GRIN2Ac.3511C>G (p.Pro1171Ala)
c.3040C>G (p.Pro1014Ala)
n.3104C>G
c.*881C>G (n.*881C>G)
c.3100C>G (p.Pro1034Ala)
n.3150C>G
c.3352C>G (p.Pro1118Ala)
c.3253C>G (p.Pro1085Ala)
c.3667C>G (p.Pro1223Ala)
 dbSNP gnomAD v4
16g.9764033G=CA2206693021GRIN2Ac.3511C= (p.Pro1171=)
c.3040C= (p.Pro1014=)
n.3104C=
c.*881C= (n.*881C=)
c.3100C= (p.Pro1034=)
n.3150C=
c.3352C= (p.Pro1118=)
c.3253C= (p.Pro1085=)
c.3667C= (p.Pro1223=)
16g.9764033G>TCA7896301GRIN2Ac.3511C>A (p.Pro1171Thr)
c.3040C>A (p.Pro1014Thr)
n.3104C>A
c.*881C>A (n.*881C>A)
c.3100C>A (p.Pro1034Thr)
n.3150C>A
c.3352C>A (p.Pro1118Thr)
c.3253C>A (p.Pro1085Thr)
c.3667C>A (p.Pro1223Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.9764034G>ACA493693365GRIN2Ac.3510C>T (p.Asn1170=)
c.3039C>T (p.Asn1013=)
n.3103C>T
c.*880C>T (n.*880C>T)
c.3099C>T (p.Asn1033=)
n.3149C>T
c.3351C>T (p.Asn1117=)
c.3252C>T (p.Asn1084=)
c.3666C>T (p.Asn1222=)
 dbSNP COSMIC
16g.9764034G>CCA394707463GRIN2Ac.3510C>G (p.Asn1170Lys)
c.3039C>G (p.Asn1013Lys)
n.3103C>G
c.*880C>G (n.*880C>G)
c.3099C>G (p.Asn1033Lys)
n.3149C>G
c.3351C>G (p.Asn1117Lys)
c.3252C>G (p.Asn1084Lys)
c.3666C>G (p.Asn1222Lys)
 dbSNP gnomAD v4
16g.9764034G>TCA394707464GRIN2Ac.3510C>A (p.Asn1170Lys)
c.3039C>A (p.Asn1013Lys)
n.3103C>A
c.*880C>A (n.*880C>A)
c.3099C>A (p.Asn1033Lys)
n.3149C>A
c.3351C>A (p.Asn1117Lys)
c.3252C>A (p.Asn1084Lys)
c.3666C>A (p.Asn1222Lys)
16g.9764034_9764035insCACA2520747057GRIN2Ac.3509_3510insTG (p.Pro1171AlafsTer24)
c.3038_3039insTG (p.Pro1014AlafsTer24)
n.3102_3103insTG
c.*879_*880insTG (n.*879_*880insTG)
c.3098_3099insTG (p.Pro1034AlafsTer24)
n.3148_3149insTG
c.3350_3351insTG (p.Pro1118AlafsTer24)
c.3251_3252insTG (p.Pro1085AlafsTer24)
c.3665_3666insTG (p.Pro1223AlafsTer24)
16g.9764034_9764035insGACTCCACGCTGCCAACA2805820127GRIN2Ac.3509_3510insTTGGCAGCGTGGAGTC (p.Pro1171TrpfsTer9)
c.3038_3039insTTGGCAGCGTGGAGTC (p.Pro1014TrpfsTer9)
n.3102_3103insTTGGCAGCGTGGAGTC
c.*879_*880insTTGGCAGCGTGGAGTC (n.*879_*880insTTGGCAGCGTGGAGTC)
c.3098_3099insTTGGCAGCGTGGAGTC (p.Pro1034TrpfsTer9)
n.3148_3149insTTGGCAGCGTGGAGTC
c.3350_3351insTTGGCAGCGTGGAGTC (p.Pro1118TrpfsTer9)
c.3251_3252insTTGGCAGCGTGGAGTC (p.Pro1085TrpfsTer9)
c.3665_3666insTTGGCAGCGTGGAGTC (p.Pro1223TrpfsTer9)
16g.9764035T>ACA394707465GRIN2Ac.3509A>T (p.Asn1170Ile)
c.3038A>T (p.Asn1013Ile)
n.3102A>T
c.*879A>T (n.*879A>T)
c.3098A>T (p.Asn1033Ile)
n.3148A>T
c.3350A>T (p.Asn1117Ile)
c.3251A>T (p.Asn1084Ile)
c.3665A>T (p.Asn1222Ile)
 dbSNP
16g.9764035T>CCA394707466GRIN2Ac.3509A>G (p.Asn1170Ser)
c.3038A>G (p.Asn1013Ser)
n.3102A>G
c.*879A>G (n.*879A>G)
c.3098A>G (p.Asn1033Ser)
n.3148A>G
c.3350A>G (p.Asn1117Ser)
c.3251A>G (p.Asn1084Ser)
c.3665A>G (p.Asn1222Ser)
16g.9764035T>GCA394707467GRIN2Ac.3509A>C (p.Asn1170Thr)
c.3038A>C (p.Asn1013Thr)
n.3102A>C
c.*879A>C (n.*879A>C)
c.3098A>C (p.Asn1033Thr)
n.3148A>C
c.3350A>C (p.Asn1117Thr)
c.3251A>C (p.Asn1084Thr)
c.3665A>C (p.Asn1222Thr)
 dbSNP
16g.9764036T>ACA394707468GRIN2Ac.3508A>T (p.Asn1170Tyr)
c.3037A>T (p.Asn1013Tyr)
n.3101A>T
c.*878A>T (n.*878A>T)
c.3097A>T (p.Asn1033Tyr)
n.3147A>T
c.3349A>T (p.Asn1117Tyr)
c.3250A>T (p.Asn1084Tyr)
c.3664A>T (p.Asn1222Tyr)
 dbSNP
16g.9764036T>CCA394707469GRIN2Ac.3508A>G (p.Asn1170Asp)
c.3037A>G (p.Asn1013Asp)
n.3101A>G
c.*878A>G (n.*878A>G)
c.3097A>G (p.Asn1033Asp)
n.3147A>G
c.3349A>G (p.Asn1117Asp)
c.3250A>G (p.Asn1084Asp)
c.3664A>G (p.Asn1222Asp)
 dbSNP
16g.9764036T>GCA394707470GRIN2Ac.3508A>C (p.Asn1170His)
c.3037A>C (p.Asn1013His)
n.3101A>C
c.*878A>C (n.*878A>C)
c.3097A>C (p.Asn1033His)
n.3147A>C
c.3349A>C (p.Asn1117His)
c.3250A>C (p.Asn1084His)
c.3664A>C (p.Asn1222His)
 dbSNP gnomAD v2 gnomAD v4
16g.9764036T=CA2206693022GRIN2Ac.3508A= (p.Asn1170=)
c.3037A= (p.Asn1013=)
n.3101A=
c.*878A= (n.*878A=)
c.3097A= (p.Asn1033=)
n.3147A=
c.3349A= (p.Asn1117=)
c.3250A= (p.Asn1084=)
c.3664A= (p.Asn1222=)
16g.9764037C>ACA493693368GRIN2Ac.3507G>T (p.Arg1169=)
c.3036G>T (p.Arg1012=)
n.3100G>T
c.*877G>T (n.*877G>T)
c.3096G>T (p.Arg1032=)
n.3146G>T
c.3348G>T (p.Arg1116=)
c.3249G>T (p.Arg1083=)
c.3663G>T (p.Arg1221=)
16g.9764037C>GCA493693369GRIN2Ac.3507G>C (p.Arg1169=)
c.3036G>C (p.Arg1012=)
n.3100G>C
c.*877G>C (n.*877G>C)
c.3096G>C (p.Arg1032=)
n.3146G>C
c.3348G>C (p.Arg1116=)
c.3249G>C (p.Arg1083=)
c.3663G>C (p.Arg1221=)
 dbSNP
16g.9764037C>TCA493693370GRIN2Ac.3507G>A (p.Arg1169=)
c.3036G>A (p.Arg1012=)
n.3100G>A
c.*877G>A (n.*877G>A)
c.3096G>A (p.Arg1032=)
n.3146G>A
c.3348G>A (p.Arg1116=)
c.3249G>A (p.Arg1083=)
c.3663G>A (p.Arg1221=)
 dbSNP gnomAD v4
16g.9764038C>ACA394707471GRIN2Ac.3506G>T (p.Arg1169Leu)
c.3035G>T (p.Arg1012Leu)
n.3099G>T
c.*876G>T (n.*876G>T)
c.3095G>T (p.Arg1032Leu)
n.3145G>T
c.3347G>T (p.Arg1116Leu)
c.3248G>T (p.Arg1083Leu)
c.3662G>T (p.Arg1221Leu)
 dbSNP
16g.9764038C=CA2206693023GRIN2Ac.3506G= (p.Arg1169=)
c.3035G= (p.Arg1012=)
n.3099G=
c.*876G= (n.*876G=)
c.3095G= (p.Arg1032=)
n.3145G=
c.3347G= (p.Arg1116=)
c.3248G= (p.Arg1083=)
c.3662G= (p.Arg1221=)
16g.9764038C>GCA394707472GRIN2Ac.3506G>C (p.Arg1169Pro)
c.3035G>C (p.Arg1012Pro)
n.3099G>C
c.*876G>C (n.*876G>C)
c.3095G>C (p.Arg1032Pro)
n.3145G>C
c.3347G>C (p.Arg1116Pro)
c.3248G>C (p.Arg1083Pro)
c.3662G>C (p.Arg1221Pro)
 dbSNP
16g.9764038C>TCA7896303GRIN2Ac.3506G>A (p.Arg1169Gln)
c.3035G>A (p.Arg1012Gln)
n.3099G>A
c.*876G>A (n.*876G>A)
c.3095G>A (p.Arg1032Gln)
n.3145G>A
c.3347G>A (p.Arg1116Gln)
c.3248G>A (p.Arg1083Gln)
c.3662G>A (p.Arg1221Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
16g.9764039G>ACA7896304GRIN2Ac.3505C>T (p.Arg1169Trp)
c.3034C>T (p.Arg1012Trp)
n.3098C>T
c.*875C>T (n.*875C>T)
c.3094C>T (p.Arg1032Trp)
n.3144C>T
c.3346C>T (p.Arg1116Trp)
c.3247C>T (p.Arg1083Trp)
c.3661C>T (p.Arg1221Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.9764039G>CCA394707474GRIN2Ac.3505C>G (p.Arg1169Gly)
c.3034C>G (p.Arg1012Gly)
n.3098C>G
c.*875C>G (n.*875C>G)
c.3094C>G (p.Arg1032Gly)
n.3144C>G
c.3346C>G (p.Arg1116Gly)
c.3247C>G (p.Arg1083Gly)
c.3661C>G (p.Arg1221Gly)
 ClinVar dbSNP
16g.9764039G=CA2206693024GRIN2Ac.3505C= (p.Arg1169=)
c.3034C= (p.Arg1012=)
n.3098C=
c.*875C= (n.*875C=)
c.3094C= (p.Arg1032=)
n.3144C=
c.3346C= (p.Arg1116=)
c.3247C= (p.Arg1083=)
c.3661C= (p.Arg1221=)
16g.9764039G>TCA493693374GRIN2Ac.3505C>A (p.Arg1169=)
c.3034C>A (p.Arg1012=)
n.3098C>A
c.*875C>A (n.*875C>A)
c.3094C>A (p.Arg1032=)
n.3144C>A
c.3346C>A (p.Arg1116=)
c.3247C>A (p.Arg1083=)
c.3661C>A (p.Arg1221=)
 dbSNP gnomAD v4 COSMIC
16g.9764040G>ACA277537199GRIN2Ac.3504C>T (p.Asn1168=)
c.3033C>T (p.Asn1011=)
n.3097C>T
c.*874C>T (n.*874C>T)
c.3093C>T (p.Asn1031=)
n.3143C>T
c.3345C>T (p.Asn1115=)
c.3246C>T (p.Asn1082=)
c.3660C>T (p.Asn1220=)
 ClinVar dbSNP gnomAD v4
16g.9764040G>CCA277537203GRIN2Ac.3504C>G (p.Asn1168Lys)
c.3033C>G (p.Asn1011Lys)
n.3097C>G
c.*874C>G (n.*874C>G)
c.3093C>G (p.Asn1031Lys)
n.3143C>G
c.3345C>G (p.Asn1115Lys)
c.3246C>G (p.Asn1082Lys)
c.3660C>G (p.Asn1220Lys)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.9764040G=CA2206693025GRIN2Ac.3504C= (p.Asn1168=)
c.3033C= (p.Asn1011=)
n.3097C=
c.*874C= (n.*874C=)
c.3093C= (p.Asn1031=)
n.3143C=
c.3345C= (p.Asn1115=)
c.3246C= (p.Asn1082=)
c.3660C= (p.Asn1220=)
16g.9764040G>TCA394707477GRIN2Ac.3504C>A (p.Asn1168Lys)
c.3033C>A (p.Asn1011Lys)
n.3097C>A
c.*874C>A (n.*874C>A)
c.3093C>A (p.Asn1031Lys)
n.3143C>A
c.3345C>A (p.Asn1115Lys)
c.3246C>A (p.Asn1082Lys)
c.3660C>A (p.Asn1220Lys)
 gnomAD v4
16g.9764041T>ACA394707484GRIN2Ac.3503A>T (p.Asn1168Ile)
c.3032A>T (p.Asn1011Ile)
n.3096A>T
c.*873A>T (n.*873A>T)
c.3092A>T (p.Asn1031Ile)
n.3142A>T
c.3344A>T (p.Asn1115Ile)
c.3245A>T (p.Asn1082Ile)
c.3659A>T (p.Asn1220Ile)
 dbSNP
16g.9764041T>CCA394707481GRIN2Ac.3503A>G (p.Asn1168Ser)
c.3032A>G (p.Asn1011Ser)
n.3096A>G
c.*873A>G (n.*873A>G)
c.3092A>G (p.Asn1031Ser)
n.3142A>G
c.3344A>G (p.Asn1115Ser)
c.3245A>G (p.Asn1082Ser)
c.3659A>G (p.Asn1220Ser)
 dbSNP
16g.9764041T>GCA394707482GRIN2Ac.3503A>C (p.Asn1168Thr)
c.3032A>C (p.Asn1011Thr)
n.3096A>C
c.*873A>C (n.*873A>C)
c.3092A>C (p.Asn1031Thr)
n.3142A>C
c.3344A>C (p.Asn1115Thr)
c.3245A>C (p.Asn1082Thr)
c.3659A>C (p.Asn1220Thr)
 dbSNP
16g.9764042T>ACA394707487GRIN2Ac.3502A>T (p.Asn1168Tyr)
c.3031A>T (p.Asn1011Tyr)
n.3095A>T
c.*872A>T (n.*872A>T)
c.3091A>T (p.Asn1031Tyr)
n.3141A>T
c.3343A>T (p.Asn1115Tyr)
c.3244A>T (p.Asn1082Tyr)
c.3658A>T (p.Asn1220Tyr)
 dbSNP
16g.9764042T>CCA394707489GRIN2Ac.3502A>G (p.Asn1168Asp)
c.3031A>G (p.Asn1011Asp)
n.3095A>G
c.*872A>G (n.*872A>G)
c.3091A>G (p.Asn1031Asp)
n.3141A>G
c.3343A>G (p.Asn1115Asp)
c.3244A>G (p.Asn1082Asp)
c.3658A>G (p.Asn1220Asp)
 dbSNP
16g.9764042T>GCA394707490GRIN2Ac.3502A>C (p.Asn1168His)
c.3031A>C (p.Asn1011His)
n.3095A>C
c.*872A>C (n.*872A>C)
c.3091A>C (p.Asn1031His)
n.3141A>C
c.3343A>C (p.Asn1115His)
c.3244A>C (p.Asn1082His)
c.3658A>C (p.Asn1220His)
16g.9764043C>ACA394707493GRIN2Ac.3501G>T (p.Met1167Ile)
c.3030G>T (p.Met1010Ile)
n.3094G>T
c.*871G>T (n.*871G>T)
c.3090G>T (p.Met1030Ile)
n.3140G>T
c.3342G>T (p.Met1114Ile)
c.3243G>T (p.Met1081Ile)
c.3657G>T (p.Met1219Ile)
 dbSNP
16g.9764043C>GCA394707495GRIN2Ac.3501G>C (p.Met1167Ile)
c.3030G>C (p.Met1010Ile)
n.3094G>C
c.*871G>C (n.*871G>C)
c.3090G>C (p.Met1030Ile)
n.3140G>C
c.3342G>C (p.Met1114Ile)
c.3243G>C (p.Met1081Ile)
c.3657G>C (p.Met1219Ile)
 dbSNP
16g.9764043C>TCA394707496GRIN2Ac.3501G>A (p.Met1167Ile)
c.3030G>A (p.Met1010Ile)
n.3094G>A
c.*871G>A (n.*871G>A)
c.3090G>A (p.Met1030Ile)
n.3140G>A
c.3342G>A (p.Met1114Ile)
c.3243G>A (p.Met1081Ile)
c.3657G>A (p.Met1219Ile)
 dbSNP
16g.9764044A>CCA394707499GRIN2Ac.3500T>G (p.Met1167Arg)
c.3029T>G (p.Met1010Arg)
n.3093T>G
c.*870T>G (n.*870T>G)
c.3089T>G (p.Met1030Arg)
n.3139T>G
c.3341T>G (p.Met1114Arg)
c.3242T>G (p.Met1081Arg)
c.3656T>G (p.Met1219Arg)
16g.9764044A>GCA394707501GRIN2Ac.3500T>C (p.Met1167Thr)
c.3029T>C (p.Met1010Thr)
n.3093T>C
c.*870T>C (n.*870T>C)
c.3089T>C (p.Met1030Thr)
n.3139T>C
c.3341T>C (p.Met1114Thr)
c.3242T>C (p.Met1081Thr)
c.3656T>C (p.Met1219Thr)
 gnomAD v4
16g.9764044A>TCA394707503GRIN2Ac.3500T>A (p.Met1167Lys)
c.3029T>A (p.Met1010Lys)
n.3093T>A
c.*870T>A (n.*870T>A)
c.3089T>A (p.Met1030Lys)
n.3139T>A
c.3341T>A (p.Met1114Lys)
c.3242T>A (p.Met1081Lys)
c.3656T>A (p.Met1219Lys)
 ClinVar dbSNP gnomAD v4
16g.9764045T>ACA394707505GRIN2Ac.3499A>T (p.Met1167Leu)
c.3028A>T (p.Met1010Leu)
n.3092A>T
c.*869A>T (n.*869A>T)
c.3088A>T (p.Met1030Leu)
n.3138A>T
c.3340A>T (p.Met1114Leu)
c.3241A>T (p.Met1081Leu)
c.3655A>T (p.Met1219Leu)
 dbSNP
16g.9764045T>CCA394707508GRIN2Ac.3499A>G (p.Met1167Val)
c.3028A>G (p.Met1010Val)
n.3092A>G
c.*869A>G (n.*869A>G)
c.3088A>G (p.Met1030Val)
n.3138A>G
c.3340A>G (p.Met1114Val)
c.3241A>G (p.Met1081Val)
c.3655A>G (p.Met1219Val)
 gnomAD v4
16g.9764045T>GCA394707510GRIN2Ac.3499A>C (p.Met1167Leu)
c.3028A>C (p.Met1010Leu)
n.3092A>C
c.*869A>C (n.*869A>C)
c.3088A>C (p.Met1030Leu)
n.3138A>C
c.3340A>C (p.Met1114Leu)
c.3241A>C (p.Met1081Leu)
c.3655A>C (p.Met1219Leu)
16g.9764046T>ACA493693379GRIN2Ac.3498A>T (p.Pro1166=)
c.3027A>T (p.Pro1009=)
n.3091A>T
c.*868A>T (n.*868A>T)
c.3087A>T (p.Pro1029=)
n.3137A>T
c.3339A>T (p.Pro1113=)
c.3240A>T (p.Pro1080=)
c.3654A>T (p.Pro1218=)
16g.9764046T>CCA493693381GRIN2Ac.3498A>G (p.Pro1166=)
c.3027A>G (p.Pro1009=)
n.3091A>G
c.*868A>G (n.*868A>G)
c.3087A>G (p.Pro1029=)
n.3137A>G
c.3339A>G (p.Pro1113=)
c.3240A>G (p.Pro1080=)
c.3654A>G (p.Pro1218=)
16g.9764046T>GCA493693382GRIN2Ac.3498A>C (p.Pro1166=)
c.3027A>C (p.Pro1009=)
n.3091A>C
c.*868A>C (n.*868A>C)
c.3087A>C (p.Pro1029=)
n.3137A>C
c.3339A>C (p.Pro1113=)
c.3240A>C (p.Pro1080=)
c.3654A>C (p.Pro1218=)
16g.9764047G>ACA394707516GRIN2Ac.3497C>T (p.Pro1166Leu)
c.3026C>T (p.Pro1009Leu)
n.3090C>T
c.*867C>T (n.*867C>T)
c.3086C>T (p.Pro1029Leu)
n.3136C>T
c.3338C>T (p.Pro1113Leu)
c.3239C>T (p.Pro1080Leu)
c.3653C>T (p.Pro1218Leu)
 dbSNP gnomAD v4
16g.9764047G>CCA394707515GRIN2Ac.3497C>G (p.Pro1166Arg)
c.3026C>G (p.Pro1009Arg)
n.3090C>G
c.*867C>G (n.*867C>G)
c.3086C>G (p.Pro1029Arg)
n.3136C>G
c.3338C>G (p.Pro1113Arg)
c.3239C>G (p.Pro1080Arg)
c.3653C>G (p.Pro1218Arg)
 dbSNP
16g.9764047G>TCA394707513GRIN2Ac.3497C>A (p.Pro1166Gln)
c.3026C>A (p.Pro1009Gln)
n.3090C>A
c.*867C>A (n.*867C>A)
c.3086C>A (p.Pro1029Gln)
n.3136C>A
c.3338C>A (p.Pro1113Gln)
c.3239C>A (p.Pro1080Gln)
c.3653C>A (p.Pro1218Gln)
 dbSNP
16g.9764048G>ACA394707521GRIN2Ac.3496C>T (p.Pro1166Ser)
c.3025C>T (p.Pro1009Ser)
n.3089C>T
c.*866C>T (n.*866C>T)
c.3085C>T (p.Pro1029Ser)
n.3135C>T
c.3337C>T (p.Pro1113Ser)
c.3238C>T (p.Pro1080Ser)
c.3652C>T (p.Pro1218Ser)
 dbSNP
16g.9764048G>CCA394707519GRIN2Ac.3496C>G (p.Pro1166Ala)
c.3025C>G (p.Pro1009Ala)
n.3089C>G
c.*866C>G (n.*866C>G)
c.3085C>G (p.Pro1029Ala)
n.3135C>G
c.3337C>G (p.Pro1113Ala)
c.3238C>G (p.Pro1080Ala)
c.3652C>G (p.Pro1218Ala)
 dbSNP
16g.9764048G>TCA394707523GRIN2Ac.3496C>A (p.Pro1166Thr)
c.3025C>A (p.Pro1009Thr)
n.3089C>A
c.*866C>A (n.*866C>A)
c.3085C>A (p.Pro1029Thr)
n.3135C>A
c.3337C>A (p.Pro1113Thr)
c.3238C>A (p.Pro1080Thr)
c.3652C>A (p.Pro1218Thr)
 dbSNP
16g.9764049C>ACA493693385GRIN2Ac.3495G>T (p.Leu1165=)
c.3024G>T (p.Leu1008=)
n.3088G>T
c.*865G>T (n.*865G>T)
c.3084G>T (p.Leu1028=)
n.3134G>T
c.3336G>T (p.Leu1112=)
c.3237G>T (p.Leu1079=)
c.3651G>T (p.Leu1217=)
 dbSNP
16g.9764049C>GCA493693386GRIN2Ac.3495G>C (p.Leu1165=)
c.3024G>C (p.Leu1008=)
n.3088G>C
c.*865G>C (n.*865G>C)
c.3084G>C (p.Leu1028=)
n.3134G>C
c.3336G>C (p.Leu1112=)
c.3237G>C (p.Leu1079=)
c.3651G>C (p.Leu1217=)
 dbSNP
16g.9764049C>TCA493693388GRIN2Ac.3495G>A (p.Leu1165=)
c.3024G>A (p.Leu1008=)
n.3088G>A
c.*865G>A (n.*865G>A)
c.3084G>A (p.Leu1028=)
n.3134G>A
c.3336G>A (p.Leu1112=)
c.3237G>A (p.Leu1079=)
c.3651G>A (p.Leu1217=)
 dbSNP
16g.9764050A>CCA394707525GRIN2Ac.3494T>G (p.Leu1165Arg)
c.3023T>G (p.Leu1008Arg)
n.3087T>G
c.*864T>G (n.*864T>G)
c.3083T>G (p.Leu1028Arg)
n.3133T>G
c.3335T>G (p.Leu1112Arg)
c.3236T>G (p.Leu1079Arg)
c.3650T>G (p.Leu1217Arg)
16g.9764050A>GCA394707529GRIN2Ac.3494T>C (p.Leu1165Pro)
c.3023T>C (p.Leu1008Pro)
n.3087T>C
c.*864T>C (n.*864T>C)
c.3083T>C (p.Leu1028Pro)
n.3133T>C
c.3335T>C (p.Leu1112Pro)
c.3236T>C (p.Leu1079Pro)
c.3650T>C (p.Leu1217Pro)
16g.9764050A>TCA394707527GRIN2Ac.3494T>A (p.Leu1165Gln)
c.3023T>A (p.Leu1008Gln)
n.3087T>A
c.*864T>A (n.*864T>A)
c.3083T>A (p.Leu1028Gln)
n.3133T>A
c.3335T>A (p.Leu1112Gln)
c.3236T>A (p.Leu1079Gln)
c.3650T>A (p.Leu1217Gln)
 dbSNP
16g.9764051G>ACA493693391GRIN2Ac.3493C>T (p.Leu1165=)
c.3022C>T (p.Leu1008=)
n.3086C>T
c.*863C>T (n.*863C>T)
c.3082C>T (p.Leu1028=)
n.3132C>T
c.3334C>T (p.Leu1112=)
c.3235C>T (p.Leu1079=)
c.3649C>T (p.Leu1217=)
 ClinVar dbSNP gnomAD v4
16g.9764051G>CCA394707532GRIN2Ac.3493C>G (p.Leu1165Val)
c.3022C>G (p.Leu1008Val)
n.3086C>G
c.*863C>G (n.*863C>G)
c.3082C>G (p.Leu1028Val)
n.3132C>G
c.3334C>G (p.Leu1112Val)
c.3235C>G (p.Leu1079Val)
c.3649C>G (p.Leu1217Val)
 dbSNP
16g.9764051G>TCA394707533GRIN2Ac.3493C>A (p.Leu1165Met)
c.3022C>A (p.Leu1008Met)
n.3086C>A
c.*863C>A (n.*863C>A)
c.3082C>A (p.Leu1028Met)
n.3132C>A
c.3334C>A (p.Leu1112Met)
c.3235C>A (p.Leu1079Met)
c.3649C>A (p.Leu1217Met)
 dbSNP gnomAD v4
16g.9764052C>ACA493693395GRIN2Ac.3492G>T (p.Thr1164=)
c.3021G>T (p.Thr1007=)
n.3085G>T
c.*862G>T (n.*862G>T)
c.3081G>T (p.Thr1027=)
n.3131G>T
c.3333G>T (p.Thr1111=)
c.3234G>T (p.Thr1078=)
c.3648G>T (p.Thr1216=)
16g.9764052C=CA2206693026GRIN2Ac.3492G= (p.Thr1164=)
c.3021G= (p.Thr1007=)
n.3085G=
c.*862G= (n.*862G=)
c.3081G= (p.Thr1027=)
n.3131G=
c.3333G= (p.Thr1111=)
c.3234G= (p.Thr1078=)
c.3648G= (p.Thr1216=)
16g.9764052C>GCA493693394GRIN2Ac.3492G>C (p.Thr1164=)
c.3021G>C (p.Thr1007=)
n.3085G>C
c.*862G>C (n.*862G>C)
c.3081G>C (p.Thr1027=)
n.3131G>C
c.3333G>C (p.Thr1111=)
c.3234G>C (p.Thr1078=)
c.3648G>C (p.Thr1216=)
 dbSNP
16g.9764052C>TCA493693393GRIN2Ac.3492G>A (p.Thr1164=)
c.3021G>A (p.Thr1007=)
n.3085G>A
c.*862G>A (n.*862G>A)
c.3081G>A (p.Thr1027=)
n.3131G>A
c.3333G>A (p.Thr1111=)
c.3234G>A (p.Thr1078=)
c.3648G>A (p.Thr1216=)
 ClinVar dbSNP gnomAD v4
16g.9764053G>ACA394707536GRIN2Ac.3491C>T (p.Thr1164Met)
c.3020C>T (p.Thr1007Met)
n.3084C>T
c.*861C>T (n.*861C>T)
c.3080C>T (p.Thr1027Met)
n.3130C>T
c.3332C>T (p.Thr1111Met)
c.3233C>T (p.Thr1078Met)
c.3647C>T (p.Thr1216Met)
 ClinVar dbSNP gnomAD v4 COSMIC
16g.9764053G>CCA394707537GRIN2Ac.3491C>G (p.Thr1164Arg)
c.3020C>G (p.Thr1007Arg)
n.3084C>G
c.*861C>G (n.*861C>G)
c.3080C>G (p.Thr1027Arg)
n.3130C>G
c.3332C>G (p.Thr1111Arg)
c.3233C>G (p.Thr1078Arg)
c.3647C>G (p.Thr1216Arg)
 dbSNP gnomAD v4
16g.9764053G>TCA394707539GRIN2Ac.3491C>A (p.Thr1164Lys)
c.3020C>A (p.Thr1007Lys)
n.3084C>A
c.*861C>A (n.*861C>A)
c.3080C>A (p.Thr1027Lys)
n.3130C>A
c.3332C>A (p.Thr1111Lys)
c.3233C>A (p.Thr1078Lys)
c.3647C>A (p.Thr1216Lys)
16g.9764054T>ACA394707542GRIN2Ac.3490A>T (p.Thr1164Ser)
c.3019A>T (p.Thr1007Ser)
n.3083A>T
c.*860A>T (n.*860A>T)
c.3079A>T (p.Thr1027Ser)
n.3129A>T
c.3331A>T (p.Thr1111Ser)
c.3232A>T (p.Thr1078Ser)
c.3646A>T (p.Thr1216Ser)
16g.9764054T>CCA394707543GRIN2Ac.3490A>G (p.Thr1164Ala)
c.3019A>G (p.Thr1007Ala)
n.3083A>G
c.*860A>G (n.*860A>G)
c.3079A>G (p.Thr1027Ala)
n.3129A>G
c.3331A>G (p.Thr1111Ala)
c.3232A>G (p.Thr1078Ala)
c.3646A>G (p.Thr1216Ala)
16g.9764054T>GCA394707544GRIN2Ac.3490A>C (p.Thr1164Pro)
c.3019A>C (p.Thr1007Pro)
n.3083A>C
c.*860A>C (n.*860A>C)
c.3079A>C (p.Thr1027Pro)
n.3129A>C
c.3331A>C (p.Thr1111Pro)
c.3232A>C (p.Thr1078Pro)
c.3646A>C (p.Thr1216Pro)
16g.9764055G>ACA493693401GRIN2Ac.3489C>T (p.Ser1163=)
c.3018C>T (p.Ser1006=)
n.3082C>T
c.*859C>T (n.*859C>T)
c.3078C>T (p.Ser1026=)
n.3128C>T
c.3330C>T (p.Ser1110=)
c.3231C>T (p.Ser1077=)
c.3645C>T (p.Ser1215=)
 dbSNP gnomAD v4
16g.9764055G>CCA7896305GRIN2Ac.3489C>G (p.Ser1163=)
c.3018C>G (p.Ser1006=)
n.3082C>G
c.*859C>G (n.*859C>G)
c.3078C>G (p.Ser1026=)
n.3128C>G
c.3330C>G (p.Ser1110=)
c.3231C>G (p.Ser1077=)
c.3645C>G (p.Ser1215=)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.9764055G=CA2206693027GRIN2Ac.3489C= (p.Ser1163=)
c.3018C= (p.Ser1006=)
n.3082C=
c.*859C= (n.*859C=)
c.3078C= (p.Ser1026=)
n.3128C=
c.3330C= (p.Ser1110=)
c.3231C= (p.Ser1077=)
c.3645C= (p.Ser1215=)
16g.9764055G>TCA493693400GRIN2Ac.3489C>A (p.Ser1163=)
c.3018C>A (p.Ser1006=)
n.3082C>A
c.*859C>A (n.*859C>A)
c.3078C>A (p.Ser1026=)
n.3128C>A
c.3330C>A (p.Ser1110=)
c.3231C>A (p.Ser1077=)
c.3645C>A (p.Ser1215=)
16g.9764056G>ACA394707548GRIN2Ac.3488C>T (p.Ser1163Phe)
c.3017C>T (p.Ser1006Phe)
n.3081C>T
c.*858C>T (n.*858C>T)
c.3077C>T (p.Ser1026Phe)
n.3127C>T
c.3329C>T (p.Ser1110Phe)
c.3230C>T (p.Ser1077Phe)
c.3644C>T (p.Ser1215Phe)
 dbSNP
16g.9764056G>CCA394707550GRIN2Ac.3488C>G (p.Ser1163Cys)
c.3017C>G (p.Ser1006Cys)
n.3081C>G
c.*858C>G (n.*858C>G)
c.3077C>G (p.Ser1026Cys)
n.3127C>G
c.3329C>G (p.Ser1110Cys)
c.3230C>G (p.Ser1077Cys)
c.3644C>G (p.Ser1215Cys)
 dbSNP
16g.9764056G=CA2206693028GRIN2Ac.3488C= (p.Ser1163=)
c.3017C= (p.Ser1006=)
n.3081C=
c.*858C= (n.*858C=)
c.3077C= (p.Ser1026=)
n.3127C=
c.3329C= (p.Ser1110=)
c.3230C= (p.Ser1077=)
c.3644C= (p.Ser1215=)
16g.9764056G>TCA394707551GRIN2Ac.3488C>A (p.Ser1163Tyr)
c.3017C>A (p.Ser1006Tyr)
n.3081C>A
c.*858C>A (n.*858C>A)
c.3077C>A (p.Ser1026Tyr)
n.3127C>A
c.3329C>A (p.Ser1110Tyr)
c.3230C>A (p.Ser1077Tyr)
c.3644C>A (p.Ser1215Tyr)
 dbSNP
16g.9764057A>CCA394707558GRIN2Ac.3487T>G (p.Ser1163Ala)
c.3016T>G (p.Ser1006Ala)
n.3080T>G
c.*857T>G (n.*857T>G)
c.3076T>G (p.Ser1026Ala)
n.3126T>G
c.3328T>G (p.Ser1110Ala)
c.3229T>G (p.Ser1077Ala)
c.3643T>G (p.Ser1215Ala)
16g.9764057A>GCA394707556GRIN2Ac.3487T>C (p.Ser1163Pro)
c.3016T>C (p.Ser1006Pro)
n.3080T>C
c.*857T>C (n.*857T>C)
c.3076T>C (p.Ser1026Pro)
n.3126T>C
c.3328T>C (p.Ser1110Pro)
c.3229T>C (p.Ser1077Pro)
c.3643T>C (p.Ser1215Pro)
 dbSNP
16g.9764057A>TCA394707554GRIN2Ac.3487T>A (p.Ser1163Thr)
c.3016T>A (p.Ser1006Thr)
n.3080T>A
c.*857T>A (n.*857T>A)
c.3076T>A (p.Ser1026Thr)
n.3126T>A
c.3328T>A (p.Ser1110Thr)
c.3229T>A (p.Ser1077Thr)
c.3643T>A (p.Ser1215Thr)
 dbSNP
16g.9764058G>ACA493693410GRIN2Ac.3486C>T (p.Asp1162=)
c.3015C>T (p.Asp1005=)
n.3079C>T
c.*856C>T (n.*856C>T)
c.3075C>T (p.Asp1025=)
n.3125C>T
c.3327C>T (p.Asp1109=)
c.3228C>T (p.Asp1076=)
c.3642C>T (p.Asp1214=)
 dbSNP
16g.9764058G>CCA394707561GRIN2Ac.3486C>G (p.Asp1162Glu)
c.3015C>G (p.Asp1005Glu)
n.3079C>G
c.*856C>G (n.*856C>G)
c.3075C>G (p.Asp1025Glu)
n.3125C>G
c.3327C>G (p.Asp1109Glu)
c.3228C>G (p.Asp1076Glu)
c.3642C>G (p.Asp1214Glu)
 dbSNP
16g.9764058G=CA2206693029GRIN2Ac.3486C= (p.Asp1162=)
c.3015C= (p.Asp1005=)
n.3079C=
c.*856C= (n.*856C=)
c.3075C= (p.Asp1025=)
n.3125C=
c.3327C= (p.Asp1109=)
c.3228C= (p.Asp1076=)
c.3642C= (p.Asp1214=)
16g.9764058G>TCA394707562GRIN2Ac.3486C>A (p.Asp1162Glu)
c.3015C>A (p.Asp1005Glu)
n.3079C>A
c.*856C>A (n.*856C>A)
c.3075C>A (p.Asp1025Glu)
n.3125C>A
c.3327C>A (p.Asp1109Glu)
c.3228C>A (p.Asp1076Glu)
c.3642C>A (p.Asp1214Glu)
16g.9764059T>ACA394707566GRIN2Ac.3485A>T (p.Asp1162Val)
c.3014A>T (p.Asp1005Val)
n.3078A>T
c.*855A>T (n.*855A>T)
c.3074A>T (p.Asp1025Val)
n.3124A>T
c.3326A>T (p.Asp1109Val)
c.3227A>T (p.Asp1076Val)
c.3641A>T (p.Asp1214Val)
 dbSNP gnomAD v4 COSMIC
16g.9764059T>CCA394707568GRIN2Ac.3485A>G (p.Asp1162Gly)
c.3014A>G (p.Asp1005Gly)
n.3078A>G
c.*855A>G (n.*855A>G)
c.3074A>G (p.Asp1025Gly)
n.3124A>G
c.3326A>G (p.Asp1109Gly)
c.3227A>G (p.Asp1076Gly)
c.3641A>G (p.Asp1214Gly)
 ClinVar
16g.9764059T>GCA394707570GRIN2Ac.3485A>C (p.Asp1162Ala)
c.3014A>C (p.Asp1005Ala)
n.3078A>C
c.*855A>C (n.*855A>C)
c.3074A>C (p.Asp1025Ala)
n.3124A>C
c.3326A>C (p.Asp1109Ala)
c.3227A>C (p.Asp1076Ala)
c.3641A>C (p.Asp1214Ala)
16g.9764060C>ACA394707573GRIN2Ac.3484G>T (p.Asp1162Tyr)
c.3013G>T (p.Asp1005Tyr)
n.3077G>T
c.*854G>T (n.*854G>T)
c.3073G>T (p.Asp1025Tyr)
n.3123G>T
c.3325G>T (p.Asp1109Tyr)
c.3226G>T (p.Asp1076Tyr)
c.3640G>T (p.Asp1214Tyr)
 dbSNP
16g.9764060C=CA2206693030GRIN2Ac.3484G= (p.Asp1162=)
c.3013G= (p.Asp1005=)
n.3077G=
c.*854G= (n.*854G=)
c.3073G= (p.Asp1025=)
n.3123G=
c.3325G= (p.Asp1109=)
c.3226G= (p.Asp1076=)
c.3640G= (p.Asp1214=)
16g.9764060C>GCA394707575GRIN2Ac.3484G>C (p.Asp1162His)
c.3013G>C (p.Asp1005His)
n.3077G>C
c.*854G>C (n.*854G>C)
c.3073G>C (p.Asp1025His)
n.3123G>C
c.3325G>C (p.Asp1109His)
c.3226G>C (p.Asp1076His)
c.3640G>C (p.Asp1214His)
 dbSNP gnomAD v2 gnomAD v4
16g.9764060C>TCA394707576GRIN2Ac.3484G>A (p.Asp1162Asn)
c.3013G>A (p.Asp1005Asn)
n.3077G>A
c.*854G>A (n.*854G>A)
c.3073G>A (p.Asp1025Asn)
n.3123G>A
c.3325G>A (p.Asp1109Asn)
c.3226G>A (p.Asp1076Asn)
c.3640G>A (p.Asp1214Asn)
 dbSNP COSMIC
16g.9764061C>ACA493693412GRIN2Ac.3483G>T (p.Gly1161=)
c.3012G>T (p.Gly1004=)
n.3076G>T
c.*853G>T (n.*853G>T)
c.3072G>T (p.Gly1024=)
n.3122G>T
c.3324G>T (p.Gly1108=)
c.3225G>T (p.Gly1075=)
c.3639G>T (p.Gly1213=)
 dbSNP
16g.9764061C=CA2206693031GRIN2Ac.3483G= (p.Gly1161=)
c.3012G= (p.Gly1004=)
n.3076G=
c.*853G= (n.*853G=)
c.3072G= (p.Gly1024=)
n.3122G=
c.3324G= (p.Gly1108=)
c.3225G= (p.Gly1075=)
c.3639G= (p.Gly1213=)
16g.9764061C>GCA7896307GRIN2Ac.3483G>C (p.Gly1161=)
c.3012G>C (p.Gly1004=)
n.3076G>C
c.*853G>C (n.*853G>C)
c.3072G>C (p.Gly1024=)
n.3122G>C
c.3324G>C (p.Gly1108=)
c.3225G>C (p.Gly1075=)
c.3639G>C (p.Gly1213=)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.9764061C>TCA7896306GRIN2Ac.3483G>A (p.Gly1161=)
c.3012G>A (p.Gly1004=)
n.3076G>A
c.*853G>A (n.*853G>A)
c.3072G>A (p.Gly1024=)
n.3122G>A
c.3324G>A (p.Gly1108=)
c.3225G>A (p.Gly1075=)
c.3639G>A (p.Gly1213=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
16g.9764062C>ACA394707580GRIN2Ac.3482G>T (p.Gly1161Val)
c.3011G>T (p.Gly1004Val)
n.3075G>T
c.*852G>T (n.*852G>T)
c.3071G>T (p.Gly1024Val)
n.3121G>T
c.3323G>T (p.Gly1108Val)
c.3224G>T (p.Gly1075Val)
c.3638G>T (p.Gly1213Val)
 dbSNP
16g.9764062C=CA2206693032GRIN2Ac.3482G= (p.Gly1161=)
c.3011G= (p.Gly1004=)
n.3075G=
c.*852G= (n.*852G=)
c.3071G= (p.Gly1024=)
n.3121G=
c.3323G= (p.Gly1108=)
c.3224G= (p.Gly1075=)
c.3638G= (p.Gly1213=)
16g.9764062C>GCA394707581GRIN2Ac.3482G>C (p.Gly1161Ala)
c.3011G>C (p.Gly1004Ala)
n.3075G>C
c.*852G>C (n.*852G>C)
c.3071G>C (p.Gly1024Ala)
n.3121G>C
c.3323G>C (p.Gly1108Ala)
c.3224G>C (p.Gly1075Ala)
c.3638G>C (p.Gly1213Ala)
 ClinVar dbSNP gnomAD v4
16g.9764062C>TCA394707583GRIN2Ac.3482G>A (p.Gly1161Glu)
c.3011G>A (p.Gly1004Glu)
n.3075G>A
c.*852G>A (n.*852G>A)
c.3071G>A (p.Gly1024Glu)
n.3121G>A
c.3323G>A (p.Gly1108Glu)
c.3224G>A (p.Gly1075Glu)
c.3638G>A (p.Gly1213Glu)
 ClinVar dbSNP
16g.9764063C>ACA394707585GRIN2Ac.3481G>T (p.Gly1161Trp)
c.3010G>T (p.Gly1004Trp)
n.3074G>T
c.*851G>T (n.*851G>T)
c.3070G>T (p.Gly1024Trp)
n.3120G>T
c.3322G>T (p.Gly1108Trp)
c.3223G>T (p.Gly1075Trp)
c.3637G>T (p.Gly1213Trp)
 dbSNP gnomAD v4
16g.9764063C>GCA394707587GRIN2Ac.3481G>C (p.Gly1161Arg)
c.3010G>C (p.Gly1004Arg)
n.3074G>C
c.*851G>C (n.*851G>C)
c.3070G>C (p.Gly1024Arg)
n.3120G>C
c.3322G>C (p.Gly1108Arg)
c.3223G>C (p.Gly1075Arg)
c.3637G>C (p.Gly1213Arg)
 dbSNP
16g.9764063C>TCA394707584GRIN2Ac.3481G>A (p.Gly1161Arg)
c.3010G>A (p.Gly1004Arg)
n.3074G>A
c.*851G>A (n.*851G>A)
c.3070G>A (p.Gly1024Arg)
n.3120G>A
c.3322G>A (p.Gly1108Arg)
c.3223G>A (p.Gly1075Arg)
c.3637G>A (p.Gly1213Arg)
 dbSNP gnomAD v4 COSMIC
16g.9764064C>ACA394707589GRIN2Ac.3480G>T (p.Lys1160Asn)
c.3009G>T (p.Lys1003Asn)
n.3073G>T
c.*850G>T (n.*850G>T)
c.3069G>T (p.Lys1023Asn)
n.3119G>T
c.3321G>T (p.Lys1107Asn)
c.3222G>T (p.Lys1074Asn)
c.3636G>T (p.Lys1212Asn)
 dbSNP gnomAD v3 gnomAD v4
16g.9764064C=CA2206693033GRIN2Ac.3480G= (p.Lys1160=)
c.3009G= (p.Lys1003=)
n.3073G=
c.*850G= (n.*850G=)
c.3069G= (p.Lys1023=)
n.3119G=
c.3321G= (p.Lys1107=)
c.3222G= (p.Lys1074=)
c.3636G= (p.Lys1212=)
16g.9764064C>GCA394707596GRIN2Ac.3480G>C (p.Lys1160Asn)
c.3009G>C (p.Lys1003Asn)
n.3073G>C
c.*850G>C (n.*850G>C)
c.3069G>C (p.Lys1023Asn)
n.3119G>C
c.3321G>C (p.Lys1107Asn)
c.3222G>C (p.Lys1074Asn)
c.3636G>C (p.Lys1212Asn)
 ClinVar dbSNP
16g.9764064C>TCA493693417GRIN2Ac.3480G>A (p.Lys1160=)
c.3009G>A (p.Lys1003=)
n.3073G>A
c.*850G>A (n.*850G>A)
c.3069G>A (p.Lys1023=)
n.3119G>A
c.3321G>A (p.Lys1107=)
c.3222G>A (p.Lys1074=)
c.3636G>A (p.Lys1212=)
 dbSNP
16g.9764065T>ACA394707599GRIN2Ac.3479A>T (p.Lys1160Met)
c.3008A>T (p.Lys1003Met)
n.3072A>T
c.*849A>T (n.*849A>T)
c.3068A>T (p.Lys1023Met)
n.3118A>T
c.3320A>T (p.Lys1107Met)
c.3221A>T (p.Lys1074Met)
c.3635A>T (p.Lys1212Met)
 dbSNP
16g.9764065T>CCA394707601GRIN2Ac.3479A>G (p.Lys1160Arg)
c.3008A>G (p.Lys1003Arg)
n.3072A>G
c.*849A>G (n.*849A>G)
c.3068A>G (p.Lys1023Arg)
n.3118A>G
c.3320A>G (p.Lys1107Arg)
c.3221A>G (p.Lys1074Arg)
c.3635A>G (p.Lys1212Arg)
 dbSNP
16g.9764065T>GCA394707603GRIN2Ac.3479A>C (p.Lys1160Thr)
c.3008A>C (p.Lys1003Thr)
n.3072A>C
c.*849A>C (n.*849A>C)
c.3068A>C (p.Lys1023Thr)
n.3118A>C
c.3320A>C (p.Lys1107Thr)
c.3221A>C (p.Lys1074Thr)
c.3635A>C (p.Lys1212Thr)
16g.9764066T>ACA394707605GRIN2Ac.3478A>T (p.Lys1160Ter)
c.3007A>T (p.Lys1003Ter)
n.3071A>T
c.*848A>T (n.*848A>T)
c.3067A>T (p.Lys1023Ter)
n.3117A>T
c.3319A>T (p.Lys1107Ter)
c.3220A>T (p.Lys1074Ter)
c.3634A>T (p.Lys1212Ter)
 dbSNP
16g.9764066T>CCA394707606GRIN2Ac.3478A>G (p.Lys1160Glu)
c.3007A>G (p.Lys1003Glu)
n.3071A>G
c.*848A>G (n.*848A>G)
c.3067A>G (p.Lys1023Glu)
n.3117A>G
c.3319A>G (p.Lys1107Glu)
c.3220A>G (p.Lys1074Glu)
c.3634A>G (p.Lys1212Glu)
 dbSNP
16g.9764066T>GCA7896308GRIN2Ac.3478A>C (p.Lys1160Gln)
c.3007A>C (p.Lys1003Gln)
n.3071A>C
c.*848A>C (n.*848A>C)
c.3067A>C (p.Lys1023Gln)
n.3117A>C
c.3319A>C (p.Lys1107Gln)
c.3220A>C (p.Lys1074Gln)
c.3634A>C (p.Lys1212Gln)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.9764066T=CA2206693034GRIN2Ac.3478A= (p.Lys1160=)
c.3007A= (p.Lys1003=)
n.3071A=
c.*848A= (n.*848A=)
c.3067A= (p.Lys1023=)
n.3117A=
c.3319A= (p.Lys1107=)
c.3220A= (p.Lys1074=)
c.3634A= (p.Lys1212=)
16g.9764067G>ACA493693420GRIN2Ac.3477C>T (p.Arg1159=)
c.3006C>T (p.Arg1002=)
n.3070C>T
c.*847C>T (n.*847C>T)
c.3066C>T (p.Arg1022=)
n.3116C>T
c.3318C>T (p.Arg1106=)
c.3219C>T (p.Arg1073=)
c.3633C>T (p.Arg1211=)
16g.9764067G>CCA493693422GRIN2Ac.3477C>G (p.Arg1159=)
c.3006C>G (p.Arg1002=)
n.3070C>G
c.*847C>G (n.*847C>G)
c.3066C>G (p.Arg1022=)
n.3116C>G
c.3318C>G (p.Arg1106=)
c.3219C>G (p.Arg1073=)
c.3633C>G (p.Arg1211=)
16g.9764067G>TCA493693425GRIN2Ac.3477C>A (p.Arg1159=)
c.3006C>A (p.Arg1002=)
n.3070C>A
c.*847C>A (n.*847C>A)
c.3066C>A (p.Arg1022=)
n.3116C>A
c.3318C>A (p.Arg1106=)
c.3219C>A (p.Arg1073=)
c.3633C>A (p.Arg1211=)
16g.9764068C>ACA7896311GRIN2Ac.3476G>T (p.Arg1159Leu)
c.3005G>T (p.Arg1002Leu)
n.3069G>T
c.*846G>T (n.*846G>T)
c.3065G>T (p.Arg1022Leu)
n.3115G>T
c.3317G>T (p.Arg1106Leu)
c.3218G>T (p.Arg1073Leu)
c.3632G>T (p.Arg1211Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.9764068C=CA2206693035GRIN2Ac.3476G= (p.Arg1159=)
c.3005G= (p.Arg1002=)
n.3069G=
c.*846G= (n.*846G=)
c.3065G= (p.Arg1022=)
n.3115G=
c.3317G= (p.Arg1106=)
c.3218G= (p.Arg1073=)
c.3632G= (p.Arg1211=)
16g.9764068C>GCA7896310GRIN2Ac.3476G>C (p.Arg1159Pro)
c.3005G>C (p.Arg1002Pro)
n.3069G>C
c.*846G>C (n.*846G>C)
c.3065G>C (p.Arg1022Pro)
n.3115G>C
c.3317G>C (p.Arg1106Pro)
c.3218G>C (p.Arg1073Pro)
c.3632G>C (p.Arg1211Pro)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
16g.9764068C>TCA7896309GRIN2Ac.3476G>A (p.Arg1159His)
c.3005G>A (p.Arg1002His)
n.3069G>A
c.*846G>A (n.*846G>A)
c.3065G>A (p.Arg1022His)
n.3115G>A
c.3317G>A (p.Arg1106His)
c.3218G>A (p.Arg1073His)
c.3632G>A (p.Arg1211His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.9764069G>ACA394707619GRIN2Ac.3475C>T (p.Arg1159Cys)
c.3004C>T (p.Arg1002Cys)
n.3068C>T
c.*845C>T (n.*845C>T)
c.3064C>T (p.Arg1022Cys)
n.3114C>T
c.3316C>T (p.Arg1106Cys)
c.3217C>T (p.Arg1073Cys)
c.3631C>T (p.Arg1211Cys)
 ClinVar dbSNP gnomAD v4 COSMIC
16g.9764069G>CCA394707615GRIN2Ac.3475C>G (p.Arg1159Gly)
c.3004C>G (p.Arg1002Gly)
n.3068C>G
c.*845C>G (n.*845C>G)
c.3064C>G (p.Arg1022Gly)
n.3114C>G
c.3316C>G (p.Arg1106Gly)
c.3217C>G (p.Arg1073Gly)
c.3631C>G (p.Arg1211Gly)
 dbSNP
16g.9764069G=CA2206693036GRIN2Ac.3475C= (p.Arg1159=)
c.3004C= (p.Arg1002=)
n.3068C=
c.*845C= (n.*845C=)
c.3064C= (p.Arg1022=)
n.3114C=
c.3316C= (p.Arg1106=)
c.3217C= (p.Arg1073=)
c.3631C= (p.Arg1211=)
16g.9764069G>TCA394707617GRIN2Ac.3475C>A (p.Arg1159Ser)
c.3004C>A (p.Arg1002Ser)
n.3068C>A
c.*845C>A (n.*845C>A)
c.3064C>A (p.Arg1022Ser)
n.3114C>A
c.3316C>A (p.Arg1106Ser)
c.3217C>A (p.Arg1073Ser)
c.3631C>A (p.Arg1211Ser)
16g.9764070dupCA2580611806GRIN2Ac.3475dup (p.Arg1159ProfsTer16)
c.3004dup (p.Arg1002ProfsTer16)
n.3068dup
c.*845dup (n.*845dup)
c.3064dup (p.Arg1022ProfsTer16)
n.3114dup
c.3316dup (p.Arg1106ProfsTer16)
c.3217dup (p.Arg1073ProfsTer16)
c.3631dup (p.Arg1211ProfsTer16)
16g.9764070G>ACA493693428GRIN2Ac.3474C>T (p.Phe1158=)
c.3003C>T (p.Phe1001=)
n.3067C>T
c.*844C>T (n.*844C>T)
c.3063C>T (p.Phe1021=)
n.3113C>T
c.3315C>T (p.Phe1105=)
c.3216C>T (p.Phe1072=)
c.3630C>T (p.Phe1210=)
 dbSNP COSMIC
16g.9764070G>CCA394707622GRIN2Ac.3474C>G (p.Phe1158Leu)
c.3003C>G (p.Phe1001Leu)
n.3067C>G
c.*844C>G (n.*844C>G)
c.3063C>G (p.Phe1021Leu)
n.3113C>G
c.3315C>G (p.Phe1105Leu)
c.3216C>G (p.Phe1072Leu)
c.3630C>G (p.Phe1210Leu)
 dbSNP
16g.9764070G>TCA394707624GRIN2Ac.3474C>A (p.Phe1158Leu)
c.3003C>A (p.Phe1001Leu)
n.3067C>A
c.*844C>A (n.*844C>A)
c.3063C>A (p.Phe1021Leu)
n.3113C>A
c.3315C>A (p.Phe1105Leu)
c.3216C>A (p.Phe1072Leu)
c.3630C>A (p.Phe1210Leu)
 COSMIC
16g.9764071A>CCA394707626GRIN2Ac.3473T>G (p.Phe1158Cys)
c.3002T>G (p.Phe1001Cys)
n.3066T>G
c.*843T>G (n.*843T>G)
c.3062T>G (p.Phe1021Cys)
n.3112T>G
c.3314T>G (p.Phe1105Cys)
c.3215T>G (p.Phe1072Cys)
c.3629T>G (p.Phe1210Cys)
 gnomAD v4
16g.9764071A>GCA394707628GRIN2Ac.3473T>C (p.Phe1158Ser)
c.3002T>C (p.Phe1001Ser)
n.3066T>C
c.*843T>C (n.*843T>C)
c.3062T>C (p.Phe1021Ser)
n.3112T>C
c.3314T>C (p.Phe1105Ser)
c.3215T>C (p.Phe1072Ser)
c.3629T>C (p.Phe1210Ser)
 dbSNP
16g.9764071A>TCA394707630GRIN2Ac.3473T>A (p.Phe1158Tyr)
c.3002T>A (p.Phe1001Tyr)
n.3066T>A
c.*843T>A (n.*843T>A)
c.3062T>A (p.Phe1021Tyr)
n.3112T>A
c.3314T>A (p.Phe1105Tyr)
c.3215T>A (p.Phe1072Tyr)
c.3629T>A (p.Phe1210Tyr)
16g.9764072A>CCA394707631GRIN2Ac.3472T>G (p.Phe1158Val)
c.3001T>G (p.Phe1001Val)
n.3065T>G
c.*842T>G (n.*842T>G)
c.3061T>G (p.Phe1021Val)
n.3111T>G
c.3313T>G (p.Phe1105Val)
c.3214T>G (p.Phe1072Val)
c.3628T>G (p.Phe1210Val)
16g.9764072A>GCA394707633GRIN2Ac.3472T>C (p.Phe1158Leu)
c.3001T>C (p.Phe1001Leu)
n.3065T>C
c.*842T>C (n.*842T>C)
c.3061T>C (p.Phe1021Leu)
n.3111T>C
c.3313T>C (p.Phe1105Leu)
c.3214T>C (p.Phe1072Leu)
c.3628T>C (p.Phe1210Leu)
16g.9764072A>TCA394707635GRIN2Ac.3472T>A (p.Phe1158Ile)
c.3001T>A (p.Phe1001Ile)
n.3065T>A
c.*842T>A (n.*842T>A)
c.3061T>A (p.Phe1021Ile)
n.3111T>A
c.3313T>A (p.Phe1105Ile)
c.3214T>A (p.Phe1072Ile)
c.3628T>A (p.Phe1210Ile)
 dbSNP
16g.9764073G>ACA277537250GRIN2Ac.3471C>T (p.Asn1157=)
c.3000C>T (p.Asn1000=)
n.3064C>T
c.*841C>T (n.*841C>T)
c.3060C>T (p.Asn1020=)
n.3110C>T
c.3312C>T (p.Asn1104=)
c.3213C>T (p.Asn1071=)
c.3627C>T (p.Asn1209=)
 dbSNP
16g.9764073G>CCA394707639GRIN2Ac.3471C>G (p.Asn1157Lys)
c.3000C>G (p.Asn1000Lys)
n.3064C>G
c.*841C>G (n.*841C>G)
c.3060C>G (p.Asn1020Lys)
n.3110C>G
c.3312C>G (p.Asn1104Lys)
c.3213C>G (p.Asn1071Lys)
c.3627C>G (p.Asn1209Lys)
 dbSNP
16g.9764073G=CA2206693037GRIN2Ac.3471C= (p.Asn1157=)
c.3000C= (p.Asn1000=)
n.3064C=
c.*841C= (n.*841C=)
c.3060C= (p.Asn1020=)
n.3110C=
c.3312C= (p.Asn1104=)
c.3213C= (p.Asn1071=)
c.3627C= (p.Asn1209=)
16g.9764073G>TCA7896312GRIN2Ac.3471C>A (p.Asn1157Lys)
c.3000C>A (p.Asn1000Lys)
n.3064C>A
c.*841C>A (n.*841C>A)
c.3060C>A (p.Asn1020Lys)
n.3110C>A
c.3312C>A (p.Asn1104Lys)
c.3213C>A (p.Asn1071Lys)
c.3627C>A (p.Asn1209Lys)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.9764074T>ACA394707644GRIN2Ac.3470A>T (p.Asn1157Ile)
c.2999A>T (p.Asn1000Ile)
n.3063A>T
c.*840A>T (n.*840A>T)
c.3059A>T (p.Asn1020Ile)
n.3109A>T
c.3311A>T (p.Asn1104Ile)
c.3212A>T (p.Asn1071Ile)
c.3626A>T (p.Asn1209Ile)
 dbSNP
16g.9764074T>CCA394707647GRIN2Ac.3470A>G (p.Asn1157Ser)
c.2999A>G (p.Asn1000Ser)
n.3063A>G
c.*840A>G (n.*840A>G)
c.3059A>G (p.Asn1020Ser)
n.3109A>G
c.3311A>G (p.Asn1104Ser)
c.3212A>G (p.Asn1071Ser)
c.3626A>G (p.Asn1209Ser)
16g.9764074T>GCA394707643GRIN2Ac.3470A>C (p.Asn1157Thr)
c.2999A>C (p.Asn1000Thr)
n.3063A>C
c.*840A>C (n.*840A>C)
c.3059A>C (p.Asn1020Thr)
n.3109A>C
c.3311A>C (p.Asn1104Thr)
c.3212A>C (p.Asn1071Thr)
c.3626A>C (p.Asn1209Thr)
 dbSNP
16g.9764075T>ACA394707653GRIN2Ac.3469A>T (p.Asn1157Tyr)
c.2998A>T (p.Asn1000Tyr)
n.3062A>T
c.*839A>T (n.*839A>T)
c.3058A>T (p.Asn1020Tyr)
n.3108A>T
c.3310A>T (p.Asn1104Tyr)
c.3211A>T (p.Asn1071Tyr)
c.3625A>T (p.Asn1209Tyr)
 dbSNP
16g.9764075T>CCA394707649GRIN2Ac.3469A>G (p.Asn1157Asp)
c.2998A>G (p.Asn1000Asp)
n.3062A>G
c.*839A>G (n.*839A>G)
c.3058A>G (p.Asn1020Asp)
n.3108A>G
c.3310A>G (p.Asn1104Asp)
c.3211A>G (p.Asn1071Asp)
c.3625A>G (p.Asn1209Asp)
16g.9764075T>GCA394707652GRIN2Ac.3469A>C (p.Asn1157His)
c.2998A>C (p.Asn1000His)
n.3062A>C
c.*839A>C (n.*839A>C)
c.3058A>C (p.Asn1020His)
n.3108A>C
c.3310A>C (p.Asn1104His)
c.3211A>C (p.Asn1071His)
c.3625A>C (p.Asn1209His)
 dbSNP
16g.9764076T>ACA7896313GRIN2Ac.3468A>T (p.Glu1156Asp)
c.2997A>T (p.Glu999Asp)
n.3061A>T
c.*838A>T (n.*838A>T)
c.3057A>T (p.Glu1019Asp)
n.3107A>T
c.3309A>T (p.Glu1103Asp)
c.3210A>T (p.Glu1070Asp)
c.3624A>T (p.Glu1208Asp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.9764076T>CCA493693437GRIN2Ac.3468A>G (p.Glu1156=)
c.2997A>G (p.Glu999=)
n.3061A>G
c.*838A>G (n.*838A>G)
c.3057A>G (p.Glu1019=)
n.3107A>G
c.3309A>G (p.Glu1103=)
c.3210A>G (p.Glu1070=)
c.3624A>G (p.Glu1208=)
 dbSNP
16g.9764076T>GCA394707657GRIN2Ac.3468A>C (p.Glu1156Asp)
c.2997A>C (p.Glu999Asp)
n.3061A>C
c.*838A>C (n.*838A>C)
c.3057A>C (p.Glu1019Asp)
n.3107A>C
c.3309A>C (p.Glu1103Asp)
c.3210A>C (p.Glu1070Asp)
c.3624A>C (p.Glu1208Asp)
16g.9764076T=CA2206693038GRIN2Ac.3468A= (p.Glu1156=)
c.2997A= (p.Glu999=)
n.3061A=
c.*838A= (n.*838A=)
c.3057A= (p.Glu1019=)
n.3107A=
c.3309A= (p.Glu1103=)
c.3210A= (p.Glu1070=)
c.3624A= (p.Glu1208=)
16g.9764077T>ACA394707659GRIN2Ac.3467A>T (p.Glu1156Val)
c.2996A>T (p.Glu999Val)
n.3060A>T
c.*837A>T (n.*837A>T)
c.3056A>T (p.Glu1019Val)
n.3106A>T
c.3308A>T (p.Glu1103Val)
c.3209A>T (p.Glu1070Val)
c.3623A>T (p.Glu1208Val)
 dbSNP
16g.9764077T>CCA394707661GRIN2Ac.3467A>G (p.Glu1156Gly)
c.2996A>G (p.Glu999Gly)
n.3060A>G
c.*837A>G (n.*837A>G)
c.3056A>G (p.Glu1019Gly)
n.3106A>G
c.3308A>G (p.Glu1103Gly)
c.3209A>G (p.Glu1070Gly)
c.3623A>G (p.Glu1208Gly)
 dbSNP gnomAD v2 gnomAD v4
16g.9764077T>GCA394707663GRIN2Ac.3467A>C (p.Glu1156Ala)
c.2996A>C (p.Glu999Ala)
n.3060A>C
c.*837A>C (n.*837A>C)
c.3056A>C (p.Glu1019Ala)
n.3106A>C
c.3308A>C (p.Glu1103Ala)
c.3209A>C (p.Glu1070Ala)
c.3623A>C (p.Glu1208Ala)
16g.9764077T=CA2206693039GRIN2Ac.3467A= (p.Glu1156=)
c.2996A= (p.Glu999=)
n.3060A=
c.*837A= (n.*837A=)
c.3056A= (p.Glu1019=)
n.3106A=
c.3308A= (p.Glu1103=)
c.3209A= (p.Glu1070=)
c.3623A= (p.Glu1208=)
16g.9764078C>ACA394707666GRIN2Ac.3466G>T (p.Glu1156Ter)
c.2995G>T (p.Glu999Ter)
n.3059G>T
c.*836G>T (n.*836G>T)
c.3055G>T (p.Glu1019Ter)
n.3105G>T
c.3307G>T (p.Glu1103Ter)
c.3208G>T (p.Glu1070Ter)
c.3622G>T (p.Glu1208Ter)
 dbSNP
16g.9764078C=CA2206693040GRIN2Ac.3466G= (p.Glu1156=)
c.2995G= (p.Glu999=)
n.3059G=
c.*836G= (n.*836G=)
c.3055G= (p.Glu1019=)
n.3105G=
c.3307G= (p.Glu1103=)
c.3208G= (p.Glu1070=)
c.3622G= (p.Glu1208=)
16g.9764078C>GCA394707668GRIN2Ac.3466G>C (p.Glu1156Gln)
c.2995G>C (p.Glu999Gln)
n.3059G>C
c.*836G>C (n.*836G>C)
c.3055G>C (p.Glu1019Gln)
n.3105G>C
c.3307G>C (p.Glu1103Gln)
c.3208G>C (p.Glu1070Gln)
c.3622G>C (p.Glu1208Gln)
 dbSNP
16g.9764078C>TCA394707669GRIN2Ac.3466G>A (p.Glu1156Lys)
c.2995G>A (p.Glu999Lys)
n.3059G>A
c.*836G>A (n.*836G>A)
c.3055G>A (p.Glu1019Lys)
n.3105G>A
c.3307G>A (p.Glu1103Lys)
c.3208G>A (p.Glu1070Lys)
c.3622G>A (p.Glu1208Lys)
 dbSNP gnomAD v4 COSMIC
16g.9764079A>CCA394707672GRIN2Ac.3465T>G (p.Ser1155Arg)
c.2994T>G (p.Ser998Arg)
n.3058T>G
c.*835T>G (n.*835T>G)
c.3054T>G (p.Ser1018Arg)
n.3104T>G
c.3306T>G (p.Ser1102Arg)
c.3207T>G (p.Ser1069Arg)
c.3621T>G (p.Ser1207Arg)
 ClinVar dbSNP
16g.9764079A>GCA493693442GRIN2Ac.3465T>C (p.Ser1155=)
c.2994T>C (p.Ser998=)
n.3058T>C
c.*835T>C (n.*835T>C)
c.3054T>C (p.Ser1018=)
n.3104T>C
c.3306T>C (p.Ser1102=)
c.3207T>C (p.Ser1069=)
c.3621T>C (p.Ser1207=)
16g.9764079A>TCA394707674GRIN2Ac.3465T>A (p.Ser1155Arg)
c.2994T>A (p.Ser998Arg)
n.3058T>A
c.*835T>A (n.*835T>A)
c.3054T>A (p.Ser1018Arg)
n.3104T>A
c.3306T>A (p.Ser1102Arg)
c.3207T>A (p.Ser1069Arg)
c.3621T>A (p.Ser1207Arg)
 dbSNP
16g.9764080C>ACA7896314GRIN2Ac.3464G>T (p.Ser1155Ile)
c.2993G>T (p.Ser998Ile)
n.3057G>T
c.*834G>T (n.*834G>T)
c.3053G>T (p.Ser1018Ile)
n.3103G>T
c.3305G>T (p.Ser1102Ile)
c.3206G>T (p.Ser1069Ile)
c.3620G>T (p.Ser1207Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
16g.9764080C=CA2206693041GRIN2Ac.3464G= (p.Ser1155=)
c.2993G= (p.Ser998=)
n.3057G=
c.*834G= (n.*834G=)
c.3053G= (p.Ser1018=)
n.3103G=
c.3305G= (p.Ser1102=)
c.3206G= (p.Ser1069=)
c.3620G= (p.Ser1207=)
16g.9764080C>GCA394707678GRIN2Ac.3464G>C (p.Ser1155Thr)
c.2993G>C (p.Ser998Thr)
n.3057G>C
c.*834G>C (n.*834G>C)
c.3053G>C (p.Ser1018Thr)
n.3103G>C
c.3305G>C (p.Ser1102Thr)
c.3206G>C (p.Ser1069Thr)
c.3620G>C (p.Ser1207Thr)
 dbSNP
16g.9764080C>TCA394707679GRIN2Ac.3464G>A (p.Ser1155Asn)
c.2993G>A (p.Ser998Asn)
n.3057G>A
c.*834G>A (n.*834G>A)
c.3053G>A (p.Ser1018Asn)
n.3103G>A
c.3305G>A (p.Ser1102Asn)
c.3206G>A (p.Ser1069Asn)
c.3620G>A (p.Ser1207Asn)
 dbSNP
16g.9764081T>ACA394707682GRIN2Ac.3463A>T (p.Ser1155Cys)
c.2992A>T (p.Ser998Cys)
n.3056A>T
c.*833A>T (n.*833A>T)
c.3052A>T (p.Ser1018Cys)
n.3102A>T
c.3304A>T (p.Ser1102Cys)
c.3205A>T (p.Ser1069Cys)
c.3619A>T (p.Ser1207Cys)
16g.9764081T>CCA394707684GRIN2Ac.3463A>G (p.Ser1155Gly)
c.2992A>G (p.Ser998Gly)
n.3056A>G
c.*833A>G (n.*833A>G)
c.3052A>G (p.Ser1018Gly)
n.3102A>G
c.3304A>G (p.Ser1102Gly)
c.3205A>G (p.Ser1069Gly)
c.3619A>G (p.Ser1207Gly)
16g.9764081T>GCA394707686GRIN2Ac.3463A>C (p.Ser1155Arg)
c.2992A>C (p.Ser998Arg)
n.3056A>C
c.*833A>C (n.*833A>C)
c.3052A>C (p.Ser1018Arg)
n.3102A>C
c.3304A>C (p.Ser1102Arg)
c.3205A>C (p.Ser1069Arg)
c.3619A>C (p.Ser1207Arg)
16g.9764082G>ACA493693447GRIN2Ac.3462C>T (p.Pro1154=)
c.2991C>T (p.Pro997=)
n.3055C>T
c.*832C>T (n.*832C>T)
c.3051C>T (p.Pro1017=)
n.3101C>T
c.3303C>T (p.Pro1101=)
c.3204C>T (p.Pro1068=)
c.3618C>T (p.Pro1206=)
 dbSNP
16g.9764082G>CCA493693448GRIN2Ac.3462C>G (p.Pro1154=)
c.2991C>G (p.Pro997=)
n.3055C>G
c.*832C>G (n.*832C>G)
c.3051C>G (p.Pro1017=)
n.3101C>G
c.3303C>G (p.Pro1101=)
c.3204C>G (p.Pro1068=)
c.3618C>G (p.Pro1206=)
16g.9764082G>TCA493693449GRIN2Ac.3462C>A (p.Pro1154=)
c.2991C>A (p.Pro997=)
n.3055C>A
c.*832C>A (n.*832C>A)
c.3051C>A (p.Pro1017=)
n.3101C>A
c.3303C>A (p.Pro1101=)
c.3204C>A (p.Pro1068=)
c.3618C>A (p.Pro1206=)
 dbSNP
16g.9764083G>ACA394707689GRIN2Ac.3461C>T (p.Pro1154Leu)
c.2990C>T (p.Pro997Leu)
n.3054C>T
c.*831C>T (n.*831C>T)
c.3050C>T (p.Pro1017Leu)
n.3100C>T
c.3302C>T (p.Pro1101Leu)
c.3203C>T (p.Pro1068Leu)
c.3617C>T (p.Pro1206Leu)
 dbSNP gnomAD v3 gnomAD v4
16g.9764083G>CCA394707691GRIN2Ac.3461C>G (p.Pro1154Arg)
c.2990C>G (p.Pro997Arg)
n.3054C>G
c.*831C>G (n.*831C>G)
c.3050C>G (p.Pro1017Arg)
n.3100C>G
c.3302C>G (p.Pro1101Arg)
c.3203C>G (p.Pro1068Arg)
c.3617C>G (p.Pro1206Arg)
 dbSNP
16g.9764083G=CA2206693042GRIN2Ac.3461C= (p.Pro1154=)
c.2990C= (p.Pro997=)
n.3054C=
c.*831C= (n.*831C=)
c.3050C= (p.Pro1017=)
n.3100C=
c.3302C= (p.Pro1101=)
c.3203C= (p.Pro1068=)
c.3617C= (p.Pro1206=)
16g.9764083G>TCA394707693GRIN2Ac.3461C>A (p.Pro1154His)
c.2990C>A (p.Pro997His)
n.3054C>A
c.*831C>A (n.*831C>A)
c.3050C>A (p.Pro1017His)
n.3100C>A
c.3302C>A (p.Pro1101His)
c.3203C>A (p.Pro1068His)
c.3617C>A (p.Pro1206His)
 dbSNP
16g.9764084G>ACA394707696GRIN2Ac.3460C>T (p.Pro1154Ser)
c.2989C>T (p.Pro997Ser)
n.3053C>T
c.*830C>T (n.*830C>T)
c.3049C>T (p.Pro1017Ser)
n.3099C>T
c.3301C>T (p.Pro1101Ser)
c.3202C>T (p.Pro1068Ser)
c.3616C>T (p.Pro1206Ser)
 dbSNP gnomAD v4
16g.9764084G>CCA394707697GRIN2Ac.3460C>G (p.Pro1154Ala)
c.2989C>G (p.Pro997Ala)
n.3053C>G
c.*830C>G (n.*830C>G)
c.3049C>G (p.Pro1017Ala)
n.3099C>G
c.3301C>G (p.Pro1101Ala)
c.3202C>G (p.Pro1068Ala)
c.3616C>G (p.Pro1206Ala)
 dbSNP
16g.9764084G=CA2206693043GRIN2Ac.3460C= (p.Pro1154=)
c.2989C= (p.Pro997=)
n.3053C=
c.*830C= (n.*830C=)
c.3049C= (p.Pro1017=)
n.3099C=
c.3301C= (p.Pro1101=)
c.3202C= (p.Pro1068=)
c.3616C= (p.Pro1206=)
16g.9764084G>TCA394707699GRIN2Ac.3460C>A (p.Pro1154Thr)
c.2989C>A (p.Pro997Thr)
n.3053C>A
c.*830C>A (n.*830C>A)
c.3049C>A (p.Pro1017Thr)
n.3099C>A
c.3301C>A (p.Pro1101Thr)
c.3202C>A (p.Pro1068Thr)
c.3616C>A (p.Pro1206Thr)
 ClinVar dbSNP gnomAD v4
16g.9764085A>CCA394707702GRIN2Ac.3459T>G (p.Asp1153Glu)
c.2988T>G (p.Asp996Glu)
n.3052T>G
c.*829T>G (n.*829T>G)
c.3048T>G (p.Asp1016Glu)
n.3098T>G
c.3300T>G (p.Asp1100Glu)
c.3201T>G (p.Asp1067Glu)
c.3615T>G (p.Asp1205Glu)
16g.9764085A>GCA493693456GRIN2Ac.3459T>C (p.Asp1153=)
c.2988T>C (p.Asp996=)
n.3052T>C
c.*829T>C (n.*829T>C)
c.3048T>C (p.Asp1016=)
n.3098T>C
c.3300T>C (p.Asp1100=)
c.3201T>C (p.Asp1067=)
c.3615T>C (p.Asp1205=)
 dbSNP
16g.9764085A>TCA394707703GRIN2Ac.3459T>A (p.Asp1153Glu)
c.2988T>A (p.Asp996Glu)
n.3052T>A
c.*829T>A (n.*829T>A)
c.3048T>A (p.Asp1016Glu)
n.3098T>A
c.3300T>A (p.Asp1100Glu)
c.3201T>A (p.Asp1067Glu)
c.3615T>A (p.Asp1205Glu)
 dbSNP
16g.9764086T>ACA394707709GRIN2Ac.3458A>T (p.Asp1153Val)
c.2987A>T (p.Asp996Val)
n.3051A>T
c.*828A>T (n.*828A>T)
c.3047A>T (p.Asp1016Val)
n.3097A>T
c.3299A>T (p.Asp1100Val)
c.3200A>T (p.Asp1067Val)
c.3614A>T (p.Asp1205Val)
 dbSNP
16g.9764086T>CCA394707711GRIN2Ac.3458A>G (p.Asp1153Gly)
c.2987A>G (p.Asp996Gly)
n.3051A>G
c.*828A>G (n.*828A>G)
c.3047A>G (p.Asp1016Gly)
n.3097A>G
c.3299A>G (p.Asp1100Gly)
c.3200A>G (p.Asp1067Gly)
c.3614A>G (p.Asp1205Gly)
16g.9764086T>GCA394707707GRIN2Ac.3458A>C (p.Asp1153Ala)
c.2987A>C (p.Asp996Ala)
n.3051A>C
c.*828A>C (n.*828A>C)
c.3047A>C (p.Asp1016Ala)
n.3097A>C
c.3299A>C (p.Asp1100Ala)
c.3200A>C (p.Asp1067Ala)
c.3614A>C (p.Asp1205Ala)
 dbSNP
16g.9764087C>ACA394707714GRIN2Ac.3457G>T (p.Asp1153Tyr)
c.2986G>T (p.Asp996Tyr)
n.3050G>T
c.*827G>T (n.*827G>T)
c.3046G>T (p.Asp1016Tyr)
n.3096G>T
c.3298G>T (p.Asp1100Tyr)
c.3199G>T (p.Asp1067Tyr)
c.3613G>T (p.Asp1205Tyr)
 ClinVar dbSNP
16g.9764087C=CA2206693044GRIN2Ac.3457G= (p.Asp1153=)
c.2986G= (p.Asp996=)
n.3050G=
c.*827G= (n.*827G=)
c.3046G= (p.Asp1016=)
n.3096G=
c.3298G= (p.Asp1100=)
c.3199G= (p.Asp1067=)
c.3613G= (p.Asp1205=)
16g.9764087C>GCA394707716GRIN2Ac.3457G>C (p.Asp1153His)
c.2986G>C (p.Asp996His)
n.3050G>C
c.*827G>C (n.*827G>C)
c.3046G>C (p.Asp1016His)
n.3096G>C
c.3298G>C (p.Asp1100His)
c.3199G>C (p.Asp1067His)
c.3613G>C (p.Asp1205His)
 dbSNP
16g.9764087C>TCA277537260GRIN2Ac.3457G>A (p.Asp1153Asn)
c.2986G>A (p.Asp996Asn)
n.3050G>A
c.*827G>A (n.*827G>A)
c.3046G>A (p.Asp1016Asn)
n.3096G>A
c.3298G>A (p.Asp1100Asn)
c.3199G>A (p.Asp1067Asn)
c.3613G>A (p.Asp1205Asn)
 dbSNP COSMIC
16g.9764088C>ACA394707719GRIN2Ac.3456G>T (p.Gln1152His)
c.2985G>T (p.Gln995His)
n.3049G>T
c.*826G>T (n.*826G>T)
c.3045G>T (p.Gln1015His)
n.3095G>T
c.3297G>T (p.Gln1099His)
c.3198G>T (p.Gln1066His)
c.3612G>T (p.Gln1204His)
 dbSNP
16g.9764088C=CA2206693045GRIN2Ac.3456G= (p.Gln1152=)
c.2985G= (p.Gln995=)
n.3049G=
c.*826G= (n.*826G=)
c.3045G= (p.Gln1015=)
n.3095G=
c.3297G= (p.Gln1099=)
c.3198G= (p.Gln1066=)
c.3612G= (p.Gln1204=)
16g.9764088C>GCA394707721GRIN2Ac.3456G>C (p.Gln1152His)
c.2985G>C (p.Gln995His)
n.3049G>C
c.*826G>C (n.*826G>C)
c.3045G>C (p.Gln1015His)
n.3095G>C
c.3297G>C (p.Gln1099His)
c.3198G>C (p.Gln1066His)
c.3612G>C (p.Gln1204His)
 ClinVar dbSNP gnomAD v3 gnomAD v4
16g.9764088C>TCA493693459GRIN2Ac.3456G>A (p.Gln1152=)
c.2985G>A (p.Gln995=)
n.3049G>A
c.*826G>A (n.*826G>A)
c.3045G>A (p.Gln1015=)
n.3095G>A
c.3297G>A (p.Gln1099=)
c.3198G>A (p.Gln1066=)
c.3612G>A (p.Gln1204=)
 dbSNP gnomAD v2 gnomAD v4 COSMIC
16g.9764089T>ACA394707724GRIN2Ac.3455A>T (p.Gln1152Leu)
c.2984A>T (p.Gln995Leu)
n.3048A>T
c.*825A>T (n.*825A>T)
c.3044A>T (p.Gln1015Leu)
n.3094A>T
c.3296A>T (p.Gln1099Leu)
c.3197A>T (p.Gln1066Leu)
c.3611A>T (p.Gln1204Leu)
 gnomAD v4
16g.9764089T>CCA394707726GRIN2Ac.3455A>G (p.Gln1152Arg)
c.2984A>G (p.Gln995Arg)
n.3048A>G
c.*825A>G (n.*825A>G)
c.3044A>G (p.Gln1015Arg)
n.3094A>G
c.3296A>G (p.Gln1099Arg)
c.3197A>G (p.Gln1066Arg)
c.3611A>G (p.Gln1204Arg)
16g.9764089T>GCA394707728GRIN2Ac.3455A>C (p.Gln1152Pro)
c.2984A>C (p.Gln995Pro)
n.3048A>C
c.*825A>C (n.*825A>C)
c.3044A>C (p.Gln1015Pro)
n.3094A>C
c.3296A>C (p.Gln1099Pro)
c.3197A>C (p.Gln1066Pro)
c.3611A>C (p.Gln1204Pro)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.9764089T=CA2206693046GRIN2Ac.3455A= (p.Gln1152=)
c.2984A= (p.Gln995=)
n.3048A=
c.*825A= (n.*825A=)
c.3044A= (p.Gln1015=)
n.3094A=
c.3296A= (p.Gln1099=)
c.3197A= (p.Gln1066=)
c.3611A= (p.Gln1204=)
16g.9764090G>ACA394707730GRIN2Ac.3454C>T (p.Gln1152Ter)
c.2983C>T (p.Gln995Ter)
n.3047C>T
c.*824C>T (n.*824C>T)
c.3043C>T (p.Gln1015Ter)
n.3093C>T
c.3295C>T (p.Gln1099Ter)
c.3196C>T (p.Gln1066Ter)
c.3610C>T (p.Gln1204Ter)
 dbSNP
16g.9764090G>CCA394707732GRIN2Ac.3454C>G (p.Gln1152Glu)
c.2983C>G (p.Gln995Glu)
n.3047C>G
c.*824C>G (n.*824C>G)
c.3043C>G (p.Gln1015Glu)
n.3093C>G
c.3295C>G (p.Gln1099Glu)
c.3196C>G (p.Gln1066Glu)
c.3610C>G (p.Gln1204Glu)
 dbSNP gnomAD v4
16g.9764090G=CA2206693047GRIN2Ac.3454C= (p.Gln1152=)
c.2983C= (p.Gln995=)
n.3047C=
c.*824C= (n.*824C=)
c.3043C= (p.Gln1015=)
n.3093C=
c.3295C= (p.Gln1099=)
c.3196C= (p.Gln1066=)
c.3610C= (p.Gln1204=)
16g.9764090G>TCA394707733GRIN2Ac.3454C>A (p.Gln1152Lys)
c.2983C>A (p.Gln995Lys)
n.3047C>A
c.*824C>A (n.*824C>A)
c.3043C>A (p.Gln1015Lys)
n.3093C>A
c.3295C>A (p.Gln1099Lys)
c.3196C>A (p.Gln1066Lys)
c.3610C>A (p.Gln1204Lys)
 dbSNP
16g.9764091G>ACA493693463GRIN2Ac.3453C>T (p.Tyr1151=)
c.2982C>T (p.Tyr994=)
n.3046C>T
c.*823C>T (n.*823C>T)
c.3042C>T (p.Tyr1014=)
n.3092C>T
c.3294C>T (p.Tyr1098=)
c.3195C>T (p.Tyr1065=)
c.3609C>T (p.Tyr1203=)
 gnomAD v4
16g.9764091G>CCA394707735GRIN2Ac.3453C>G (p.Tyr1151Ter)
c.2982C>G (p.Tyr994Ter)
n.3046C>G
c.*823C>G (n.*823C>G)
c.3042C>G (p.Tyr1014Ter)
n.3092C>G
c.3294C>G (p.Tyr1098Ter)
c.3195C>G (p.Tyr1065Ter)
c.3609C>G (p.Tyr1203Ter)
 dbSNP
16g.9764091G>TCA394707737GRIN2Ac.3453C>A (p.Tyr1151Ter)
c.2982C>A (p.Tyr994Ter)
n.3046C>A
c.*823C>A (n.*823C>A)
c.3042C>A (p.Tyr1014Ter)
n.3092C>A
c.3294C>A (p.Tyr1098Ter)
c.3195C>A (p.Tyr1065Ter)
c.3609C>A (p.Tyr1203Ter)
 dbSNP
16g.9764092T>ACA394707835GRIN2Ac.3452A>T (p.Tyr1151Phe)
c.2981A>T (p.Tyr994Phe)
n.3045A>T
c.*822A>T (n.*822A>T)
c.3041A>T (p.Tyr1014Phe)
n.3091A>T
c.3293A>T (p.Tyr1098Phe)
c.3194A>T (p.Tyr1065Phe)
c.3608A>T (p.Tyr1203Phe)
 dbSNP
16g.9764092T>CCA394707834GRIN2Ac.3452A>G (p.Tyr1151Cys)
c.2981A>G (p.Tyr994Cys)
n.3045A>G
c.*822A>G (n.*822A>G)
c.3041A>G (p.Tyr1014Cys)
n.3091A>G
c.3293A>G (p.Tyr1098Cys)
c.3194A>G (p.Tyr1065Cys)
c.3608A>G (p.Tyr1203Cys)
 dbSNP COSMIC
16g.9764092T>GCA394707833GRIN2Ac.3452A>C (p.Tyr1151Ser)
c.2981A>C (p.Tyr994Ser)
n.3045A>C
c.*822A>C (n.*822A>C)
c.3041A>C (p.Tyr1014Ser)
n.3091A>C
c.3293A>C (p.Tyr1098Ser)
c.3194A>C (p.Tyr1065Ser)
c.3608A>C (p.Tyr1203Ser)
 dbSNP gnomAD v2 gnomAD v4
16g.9764092T=CA2206693048GRIN2Ac.3452A= (p.Tyr1151=)
c.2981A= (p.Tyr994=)
n.3045A=
c.*822A= (n.*822A=)
c.3041A= (p.Tyr1014=)
n.3091A=
c.3293A= (p.Tyr1098=)
c.3194A= (p.Tyr1065=)
c.3608A= (p.Tyr1203=)
16g.9764093A=CA2206693049GRIN2Ac.3451T= (p.Tyr1151=)
c.2980T= (p.Tyr994=)
n.3044T=
c.*821T= (n.*821T=)
c.3040T= (p.Tyr1014=)
n.3090T=
c.3292T= (p.Tyr1098=)
c.3193T= (p.Tyr1065=)
c.3607T= (p.Tyr1203=)
16g.9764093A>CCA394707836GRIN2Ac.3451T>G (p.Tyr1151Asp)
c.2980T>G (p.Tyr994Asp)
n.3044T>G
c.*821T>G (n.*821T>G)
c.3040T>G (p.Tyr1014Asp)
n.3090T>G
c.3292T>G (p.Tyr1098Asp)
c.3193T>G (p.Tyr1065Asp)
c.3607T>G (p.Tyr1203Asp)
16g.9764093A>GCA394707837GRIN2Ac.3451T>C (p.Tyr1151His)
c.2980T>C (p.Tyr994His)
n.3044T>C
c.*821T>C (n.*821T>C)
c.3040T>C (p.Tyr1014His)
n.3090T>C
c.3292T>C (p.Tyr1098His)
c.3193T>C (p.Tyr1065His)
c.3607T>C (p.Tyr1203His)
 ClinVar dbSNP
16g.9764093A>TCA315023GRIN2Ac.3451T>A (p.Tyr1151Asn)
c.2980T>A (p.Tyr994Asn)
n.3044T>A
c.*821T>A (n.*821T>A)
c.3040T>A (p.Tyr1014Asn)
n.3090T>A
c.3292T>A (p.Tyr1098Asn)
c.3193T>A (p.Tyr1065Asn)
c.3607T>A (p.Tyr1203Asn)
 dbSNP
16g.9764094G>ACA493692829GRIN2Ac.3450C>T (p.Pro1150=)
c.2979C>T (p.Pro993=)
n.3043C>T
c.*820C>T (n.*820C>T)
c.3039C>T (p.Pro1013=)
n.3089C>T
c.3291C>T (p.Pro1097=)
c.3192C>T (p.Pro1064=)
c.3606C>T (p.Pro1202=)
 dbSNP
16g.9764094G>CCA493692830GRIN2Ac.3450C>G (p.Pro1150=)
c.2979C>G (p.Pro993=)
n.3043C>G
c.*820C>G (n.*820C>G)
c.3039C>G (p.Pro1013=)
n.3089C>G
c.3291C>G (p.Pro1097=)
c.3192C>G (p.Pro1064=)
c.3606C>G (p.Pro1202=)
 dbSNP
16g.9764094G>TCA493692831GRIN2Ac.3450C>A (p.Pro1150=)
c.2979C>A (p.Pro993=)
n.3043C>A
c.*820C>A (n.*820C>A)
c.3039C>A (p.Pro1013=)
n.3089C>A
c.3291C>A (p.Pro1097=)
c.3192C>A (p.Pro1064=)
c.3606C>A (p.Pro1202=)
16g.9764095G>ACA394707838GRIN2Ac.3449C>T (p.Pro1150Leu)
c.2978C>T (p.Pro993Leu)
n.3042C>T
c.*819C>T (n.*819C>T)
c.3038C>T (p.Pro1013Leu)
n.3088C>T
c.3290C>T (p.Pro1097Leu)
c.3191C>T (p.Pro1064Leu)
c.3605C>T (p.Pro1202Leu)
 dbSNP
16g.9764095G>CCA394707839GRIN2Ac.3449C>G (p.Pro1150Arg)
c.2978C>G (p.Pro993Arg)
n.3042C>G
c.*819C>G (n.*819C>G)
c.3038C>G (p.Pro1013Arg)
n.3088C>G
c.3290C>G (p.Pro1097Arg)
c.3191C>G (p.Pro1064Arg)
c.3605C>G (p.Pro1202Arg)
 dbSNP
16g.9764095G>TCA394707840GRIN2Ac.3449C>A (p.Pro1150His)
c.2978C>A (p.Pro993His)
n.3042C>A
c.*819C>A (n.*819C>A)
c.3038C>A (p.Pro1013His)
n.3088C>A
c.3290C>A (p.Pro1097His)
c.3191C>A (p.Pro1064His)
c.3605C>A (p.Pro1202His)
 dbSNP
16g.9764096G>ACA394707841GRIN2Ac.3448C>T (p.Pro1150Ser)
c.2977C>T (p.Pro993Ser)
n.3041C>T
c.*818C>T (n.*818C>T)
c.3037C>T (p.Pro1013Ser)
n.3087C>T
c.3289C>T (p.Pro1097Ser)
c.3190C>T (p.Pro1064Ser)
c.3604C>T (p.Pro1202Ser)
 dbSNP gnomAD v4
16g.9764096G>CCA394707842GRIN2Ac.3448C>G (p.Pro1150Ala)
c.2977C>G (p.Pro993Ala)
n.3041C>G
c.*818C>G (n.*818C>G)
c.3037C>G (p.Pro1013Ala)
n.3087C>G
c.3289C>G (p.Pro1097Ala)
c.3190C>G (p.Pro1064Ala)
c.3604C>G (p.Pro1202Ala)
 dbSNP
16g.9764096G=CA2206693050GRIN2Ac.3448C= (p.Pro1150=)
c.2977C= (p.Pro993=)
n.3041C=
c.*818C= (n.*818C=)
c.3037C= (p.Pro1013=)
n.3087C=
c.3289C= (p.Pro1097=)
c.3190C= (p.Pro1064=)
c.3604C= (p.Pro1202=)
16g.9764096G>TCA394707843GRIN2Ac.3448C>A (p.Pro1150Thr)
c.2977C>A (p.Pro993Thr)
n.3041C>A
c.*818C>A (n.*818C>A)
c.3037C>A (p.Pro1013Thr)
n.3087C>A
c.3289C>A (p.Pro1097Thr)
c.3190C>A (p.Pro1064Thr)
c.3604C>A (p.Pro1202Thr)
 dbSNP
16g.9764097G>ACA493692832GRIN2Ac.3447C>T (p.Asp1149=)
c.2976C>T (p.Asp992=)
n.3040C>T
c.*817C>T (n.*817C>T)
c.3036C>T (p.Asp1012=)
n.3086C>T
c.3288C>T (p.Asp1096=)
c.3189C>T (p.Asp1063=)
c.3603C>T (p.Asp1201=)
 ClinVar dbSNP gnomAD v4
16g.9764097G>CCA394707844GRIN2Ac.3447C>G (p.Asp1149Glu)
c.2976C>G (p.Asp992Glu)
n.3040C>G
c.*817C>G (n.*817C>G)
c.3036C>G (p.Asp1012Glu)
n.3086C>G
c.3288C>G (p.Asp1096Glu)
c.3189C>G (p.Asp1063Glu)
c.3603C>G (p.Asp1201Glu)
 dbSNP
16g.9764097G>TCA394707845GRIN2Ac.3447C>A (p.Asp1149Glu)
c.2976C>A (p.Asp992Glu)
n.3040C>A
c.*817C>A (n.*817C>A)
c.3036C>A (p.Asp1012Glu)
n.3086C>A
c.3288C>A (p.Asp1096Glu)
c.3189C>A (p.Asp1063Glu)
c.3603C>A (p.Asp1201Glu)
 dbSNP
16g.9764098T>ACA394707846GRIN2Ac.3446A>T (p.Asp1149Val)
c.2975A>T (p.Asp992Val)
n.3039A>T
c.*816A>T (n.*816A>T)
c.3035A>T (p.Asp1012Val)
n.3085A>T
c.3287A>T (p.Asp1096Val)
c.3188A>T (p.Asp1063Val)
c.3602A>T (p.Asp1201Val)
 ClinVar dbSNP
16g.9764098T>CCA394707847GRIN2Ac.3446A>G (p.Asp1149Gly)
c.2975A>G (p.Asp992Gly)
n.3039A>G
c.*816A>G (n.*816A>G)
c.3035A>G (p.Asp1012Gly)
n.3085A>G
c.3287A>G (p.Asp1096Gly)
c.3188A>G (p.Asp1063Gly)
c.3602A>G (p.Asp1201Gly)
 dbSNP
16g.9764098T>GCA394707848GRIN2Ac.3446A>C (p.Asp1149Ala)
c.2975A>C (p.Asp992Ala)
n.3039A>C
c.*816A>C (n.*816A>C)
c.3035A>C (p.Asp1012Ala)
n.3085A>C
c.3287A>C (p.Asp1096Ala)
c.3188A>C (p.Asp1063Ala)
c.3602A>C (p.Asp1201Ala)
 dbSNP
16g.9764099C>ACA394707850GRIN2Ac.3445G>T (p.Asp1149Tyr)
c.2974G>T (p.Asp992Tyr)
n.3038G>T
c.*815G>T (n.*815G>T)
c.3034G>T (p.Asp1012Tyr)
n.3084G>T
c.3286G>T (p.Asp1096Tyr)
c.3187G>T (p.Asp1063Tyr)
c.3601G>T (p.Asp1201Tyr)
 dbSNP
16g.9764099C>GCA394707851GRIN2Ac.3445G>C (p.Asp1149His)
c.2974G>C (p.Asp992His)
n.3038G>C
c.*815G>C (n.*815G>C)
c.3034G>C (p.Asp1012His)
n.3084G>C
c.3286G>C (p.Asp1096His)
c.3187G>C (p.Asp1063His)
c.3601G>C (p.Asp1201His)
 dbSNP
16g.9764099C>TCA394707849GRIN2Ac.3445G>A (p.Asp1149Asn)
c.2974G>A (p.Asp992Asn)
n.3038G>A
c.*815G>A (n.*815G>A)
c.3034G>A (p.Asp1012Asn)
n.3084G>A
c.3286G>A (p.Asp1096Asn)
c.3187G>A (p.Asp1063Asn)
c.3601G>A (p.Asp1201Asn)
 dbSNP gnomAD v4
16g.9764100C>ACA493692841GRIN2Ac.3444G>T (p.Pro1148=)
c.2973G>T (p.Pro991=)
n.3037G>T
c.*814G>T (n.*814G>T)
c.3033G>T (p.Pro1011=)
n.3083G>T
c.3285G>T (p.Pro1095=)
c.3186G>T (p.Pro1062=)
c.3600G>T (p.Pro1200=)
 ClinVar COSMIC
16g.9764100C=CA2206693051GRIN2Ac.3444G= (p.Pro1148=)
c.2973G= (p.Pro991=)
n.3037G=
c.*814G= (n.*814G=)
c.3033G= (p.Pro1011=)
n.3083G=
c.3285G= (p.Pro1095=)
c.3186G= (p.Pro1062=)
c.3600G= (p.Pro1200=)
16g.9764100C>GCA493692836GRIN2Ac.3444G>C (p.Pro1148=)
c.2973G>C (p.Pro991=)
n.3037G>C
c.*814G>C (n.*814G>C)
c.3033G>C (p.Pro1011=)
n.3083G>C
c.3285G>C (p.Pro1095=)
c.3186G>C (p.Pro1062=)
c.3600G>C (p.Pro1200=)
16g.9764100C>TCA493692838GRIN2Ac.3444G>A (p.Pro1148=)
c.2973G>A (p.Pro991=)
n.3037G>A
c.*814G>A (n.*814G>A)
c.3033G>A (p.Pro1011=)
n.3083G>A
c.3285G>A (p.Pro1095=)
c.3186G>A (p.Pro1062=)
c.3600G>A (p.Pro1200=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.9764101G>ACA7896315GRIN2Ac.3443C>T (p.Pro1148Leu)
c.2972C>T (p.Pro991Leu)
n.3036C>T
c.*813C>T (n.*813C>T)
c.3032C>T (p.Pro1011Leu)
n.3082C>T
c.3284C>T (p.Pro1095Leu)
c.3185C>T (p.Pro1062Leu)
c.3599C>T (p.Pro1200Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
16g.9764101G>CCA394707852GRIN2Ac.3443C>G (p.Pro1148Arg)
c.2972C>G (p.Pro991Arg)
n.3036C>G
c.*813C>G (n.*813C>G)
c.3032C>G (p.Pro1011Arg)
n.3082C>G
c.3284C>G (p.Pro1095Arg)
c.3185C>G (p.Pro1062Arg)
c.3599C>G (p.Pro1200Arg)
 dbSNP
16g.9764101G=CA2206693052GRIN2Ac.3443C= (p.Pro1148=)
c.2972C= (p.Pro991=)
n.3036C=
c.*813C= (n.*813C=)
c.3032C= (p.Pro1011=)
n.3082C=
c.3284C= (p.Pro1095=)
c.3185C= (p.Pro1062=)
c.3599C= (p.Pro1200=)
16g.9764101G>TCA394707853GRIN2Ac.3443C>A (p.Pro1148Gln)
c.2972C>A (p.Pro991Gln)
n.3036C>A
c.*813C>A (n.*813C>A)
c.3032C>A (p.Pro1011Gln)
n.3082C>A
c.3284C>A (p.Pro1095Gln)
c.3185C>A (p.Pro1062Gln)
c.3599C>A (p.Pro1200Gln)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.9764102G>ACA394707854GRIN2Ac.3442C>T (p.Pro1148Ser)
c.2971C>T (p.Pro991Ser)
n.3035C>T
c.*812C>T (n.*812C>T)
c.3031C>T (p.Pro1011Ser)
n.3081C>T
c.3283C>T (p.Pro1095Ser)
c.3184C>T (p.Pro1062Ser)
c.3598C>T (p.Pro1200Ser)
 dbSNP gnomAD v4 COSMIC
16g.9764102G>CCA394707855GRIN2Ac.3442C>G (p.Pro1148Ala)
c.2971C>G (p.Pro991Ala)
n.3035C>G
c.*812C>G (n.*812C>G)
c.3031C>G (p.Pro1011Ala)
n.3081C>G
c.3283C>G (p.Pro1095Ala)
c.3184C>G (p.Pro1062Ala)
c.3598C>G (p.Pro1200Ala)
 dbSNP
16g.9764102G>TCA394707856GRIN2Ac.3442C>A (p.Pro1148Thr)
c.2971C>A (p.Pro991Thr)
n.3035C>A
c.*812C>A (n.*812C>A)
c.3031C>A (p.Pro1011Thr)
n.3081C>A
c.3283C>A (p.Pro1095Thr)
c.3184C>A (p.Pro1062Thr)
c.3598C>A (p.Pro1200Thr)
 dbSNP
16g.9764103G>ACA493692845GRIN2Ac.3441C>T (p.Phe1147=)
c.2970C>T (p.Phe990=)
n.3034C>T
c.*811C>T (n.*811C>T)
c.3030C>T (p.Phe1010=)
n.3080C>T
c.3282C>T (p.Phe1094=)
c.3183C>T (p.Phe1061=)
c.3597C>T (p.Phe1199=)
 ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
16g.9764103G>CCA394707857GRIN2Ac.3441C>G (p.Phe1147Leu)
c.2970C>G (p.Phe990Leu)
n.3034C>G
c.*811C>G (n.*811C>G)
c.3030C>G (p.Phe1010Leu)
n.3080C>G
c.3282C>G (p.Phe1094Leu)
c.3183C>G (p.Phe1061Leu)
c.3597C>G (p.Phe1199Leu)
 dbSNP
16g.9764103G=CA2206693053GRIN2Ac.3441C= (p.Phe1147=)
c.2970C= (p.Phe990=)
n.3034C=
c.*811C= (n.*811C=)
c.3030C= (p.Phe1010=)
n.3080C=
c.3282C= (p.Phe1094=)
c.3183C= (p.Phe1061=)
c.3597C= (p.Phe1199=)
16g.9764103G>TCA394707858GRIN2Ac.3441C>A (p.Phe1147Leu)
c.2970C>A (p.Phe990Leu)
n.3034C>A
c.*811C>A (n.*811C>A)
c.3030C>A (p.Phe1010Leu)
n.3080C>A
c.3282C>A (p.Phe1094Leu)
c.3183C>A (p.Phe1061Leu)
c.3597C>A (p.Phe1199Leu)
 dbSNP
16g.9764104A>CCA394707859GRIN2Ac.3440T>G (p.Phe1147Cys)
c.2969T>G (p.Phe990Cys)
n.3033T>G
c.*810T>G (n.*810T>G)
c.3029T>G (p.Phe1010Cys)
n.3079T>G
c.3281T>G (p.Phe1094Cys)
c.3182T>G (p.Phe1061Cys)
c.3596T>G (p.Phe1199Cys)
16g.9764104A>GCA394707860GRIN2Ac.3440T>C (p.Phe1147Ser)
c.2969T>C (p.Phe990Ser)
n.3033T>C
c.*810T>C (n.*810T>C)
c.3029T>C (p.Phe1010Ser)
n.3079T>C
c.3281T>C (p.Phe1094Ser)
c.3182T>C (p.Phe1061Ser)
c.3596T>C (p.Phe1199Ser)
 dbSNP
16g.9764104A>TCA394707861GRIN2Ac.3440T>A (p.Phe1147Tyr)
c.2969T>A (p.Phe990Tyr)
n.3033T>A
c.*810T>A (n.*810T>A)
c.3029T>A (p.Phe1010Tyr)
n.3079T>A
c.3281T>A (p.Phe1094Tyr)
c.3182T>A (p.Phe1061Tyr)
c.3596T>A (p.Phe1199Tyr)
 dbSNP

Number of alleles fetched