Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.13866017C>ACA478853887GRIN2Bc.192G>T (p.Val64=)
12g.13866017C>GCA478853889GRIN2Bc.192G>C (p.Val64=)
12g.13866017C>TCA478853888GRIN2Bc.192G>A (p.Val64=)
12g.13866018A>CCA384054541GRIN2Bc.191T>G (p.Val64Gly)
12g.13866018A>GCA384054542GRIN2Bc.191T>C (p.Val64Ala)
12g.13866018A>TCA384054544GRIN2Bc.191T>A (p.Val64Glu)
12g.13866019C>ACA6461445GRIN2Bc.190G>T (p.Val64Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.13866019C=CA2017578233GRIN2Bc.190G= (p.Val64=)
12g.13866019C>GCA384054548GRIN2Bc.190G>C (p.Val64Leu)
dbSNP
12g.13866019C>TCA315042GRIN2Bc.190G>A (p.Val64Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.13866020G>ACA6461447GRIN2Bc.189C>T (p.Ser63=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.13866020G>CCA478853890GRIN2Bc.189C>G (p.Ser63=)
12g.13866020G=CA2017578234GRIN2Bc.189C= (p.Ser63=)
12g.13866020G>TCA6461446GRIN2Bc.189C>A (p.Ser63=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.13866021G>ACA384054552GRIN2Bc.188C>T (p.Ser63Phe)
ClinVar dbSNP gnomAD v4
12g.13866021G>CCA384054554GRIN2Bc.188C>G (p.Ser63Cys)
12g.13866021G=CA2017578235GRIN2Bc.188C= (p.Ser63=)
12g.13866021G>TCA384054556GRIN2Bc.188C>A (p.Ser63Tyr)
12g.13866022A>CCA384054564GRIN2Bc.187T>G (p.Ser63Ala)
12g.13866022A>GCA384054566GRIN2Bc.187T>C (p.Ser63Pro)
ClinVar dbSNP
12g.13866022A>TCA384054562GRIN2Bc.187T>A (p.Ser63Thr)
12g.13866023G>ACA478853891GRIN2Bc.186C>T (p.Leu62=)
12g.13866023G>CCA478853892GRIN2Bc.186C>G (p.Leu62=)
gnomAD v4
12g.13866023G>TCA478853893GRIN2Bc.186C>A (p.Leu62=)
COSMIC
12g.13866024A=CA2017578236GRIN2Bc.185T= (p.Leu62=)
12g.13866024A>CCA384054575GRIN2Bc.185T>G (p.Leu62Arg)
12g.13866024A>GCA6461448GRIN2Bc.185T>C (p.Leu62Pro)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.13866024A>TCA384054572GRIN2Bc.185T>A (p.Leu62His)
12g.13866025G>ACA384054579GRIN2Bc.184C>T (p.Leu62Phe)
12g.13866025G>CCA384054581GRIN2Bc.184C>G (p.Leu62Val)
12g.13866025G>TCA384054583GRIN2Bc.184C>A (p.Leu62Ile)
12g.13866026A>CCA384054585GRIN2Bc.183T>G (p.His61Gln)
12g.13866026A>GCA478853894GRIN2Bc.183T>C (p.His61=)
gnomAD v4
12g.13866026A>TCA384054586GRIN2Bc.183T>A (p.His61Gln)
12g.13866027T>ACA384054588GRIN2Bc.182A>T (p.His61Leu)
12g.13866027T>CCA384054590GRIN2Bc.182A>G (p.His61Arg)
ClinVar dbSNP
12g.13866027T>GCA384054592GRIN2Bc.182A>C (p.His61Pro)
12g.13866027T=CA2017578237GRIN2Bc.182A= (p.His61=)
12g.13866030_13866032delCA2740090809GRIN2Bc.180_182del (p.His61del)
ClinVar
12g.13866028G>ACA6461449GRIN2Bc.181C>T (p.His61Tyr)
dbSNP ExAC gnomAD v2
12g.13866028G>CCA384054596GRIN2Bc.181C>G (p.His61Asp)
12g.13866028G=CA2017578238GRIN2Bc.181C= (p.His61=)
12g.13866028G>TCA384054598GRIN2Bc.181C>A (p.His61Asn)
12g.13866029G>ACA478853895GRIN2Bc.180C>T (p.His60=)
ClinVar gnomAD v4
12g.13866029G>CCA384054604GRIN2Bc.180C>G (p.His60Gln)
12g.13866029G>TCA384054602GRIN2Bc.180C>A (p.His60Gln)
12g.13866030T>ACA384054607GRIN2Bc.179A>T (p.His60Leu)
12g.13866030T>CCA384054608GRIN2Bc.179A>G (p.His60Arg)
12g.13866030T>GCA384054611GRIN2Bc.179A>C (p.His60Pro)
dbSNP
12g.13866030T=CA2017578239GRIN2Bc.179A= (p.His60=)
12g.13866031G>ACA384054614GRIN2Bc.178C>T (p.His60Tyr)
gnomAD v4
12g.13866031G>CCA384054616GRIN2Bc.178C>G (p.His60Asp)
12g.13866031G>TCA384054618GRIN2Bc.178C>A (p.His60Asn)
12g.13866032G>ACA478853896GRIN2Bc.177C>T (p.Phe59=)
12g.13866032G>CCA384054620GRIN2Bc.177C>G (p.Phe59Leu)
12g.13866032G>TCA384054621GRIN2Bc.177C>A (p.Phe59Leu)
gnomAD v4
12g.13866033A>CCA384054622GRIN2Bc.176T>G (p.Phe59Cys)
12g.13866033A>GCA384054625GRIN2Bc.176T>C (p.Phe59Ser)
gnomAD v4
12g.13866033A>TCA384054626GRIN2Bc.176T>A (p.Phe59Tyr)
12g.13866034A>CCA384054629GRIN2Bc.175T>G (p.Phe59Val)
12g.13866034A>GCA384054630GRIN2Bc.175T>C (p.Phe59Leu)
12g.13866034A>TCA384054632GRIN2Bc.175T>A (p.Phe59Ile)
12g.13866035A=CA2017578240GRIN2Bc.174T= (p.Asp58=)
12g.13866035A>CCA384054638GRIN2Bc.174T>G (p.Asp58Glu)
12g.13866035A>GCA478853897GRIN2Bc.174T>C (p.Asp58=)
ClinVar dbSNP
12g.13866035A>TCA384054636GRIN2Bc.174T>A (p.Asp58Glu)
12g.13866036T>ACA384054641GRIN2Bc.173A>T (p.Asp58Val)
12g.13866036T>CCA384054643GRIN2Bc.173A>G (p.Asp58Gly)
12g.13866036T>GCA384054645GRIN2Bc.173A>C (p.Asp58Ala)
12g.13866037C>ACA384054647GRIN2Bc.172G>T (p.Asp58Tyr)
12g.13866037C>GCA384054650GRIN2Bc.172G>C (p.Asp58His)
12g.13866037C>TCA384054652GRIN2Bc.172G>A (p.Asp58Asn)
12g.13866038A>CCA384054655GRIN2Bc.171T>G (p.Asp57Glu)
12g.13866038A>GCA478853898GRIN2Bc.171T>C (p.Asp57=)
12g.13866038A>TCA384054657GRIN2Bc.171T>A (p.Asp57Glu)
gnomAD v4
12g.13866039T>ACA233148012GRIN2Bc.170A>T (p.Asp57Val)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.13866039T>CCA384054663GRIN2Bc.170A>G (p.Asp57Gly)
dbSNP gnomAD v4
12g.13866039T>GCA384054665GRIN2Bc.170A>C (p.Asp57Ala)
12g.13866039T=CA2017578241GRIN2Bc.170A= (p.Asp57=)
12g.13866040C>ACA384054668GRIN2Bc.169G>T (p.Asp57Tyr)
12g.13866040C=CA2017578242GRIN2Bc.169G= (p.Asp57=)
12g.13866040C>GCA384054670GRIN2Bc.169G>C (p.Asp57His)
12g.13866040C>TCA384054672GRIN2Bc.169G>A (p.Asp57Asn)
dbSNP
12g.13866041T>ACA384054677GRIN2Bc.168A>T (p.Lys56Asn)
12g.13866041T>CCA478853899GRIN2Bc.168A>G (p.Lys56=)
12g.13866041T>GCA384054674GRIN2Bc.168A>C (p.Lys56Asn)
12g.13866042T>ACA384054681GRIN2Bc.167A>T (p.Lys56Ile)
12g.13866042T>CCA384054683GRIN2Bc.167A>G (p.Lys56Arg)
12g.13866042T>GCA384054685GRIN2Bc.167A>C (p.Lys56Thr)
12g.13866043T>ACA384054688GRIN2Bc.166A>T (p.Lys56Ter)
dbSNP
12g.13866043T>CCA384054690GRIN2Bc.166A>G (p.Lys56Glu)
12g.13866043T>GCA384054692GRIN2Bc.166A>C (p.Lys56Gln)
12g.13866043T=CA2017578243GRIN2Bc.166A= (p.Lys56=)
12g.13866044C>ACA384054698GRIN2Bc.165G>T (p.Glu55Asp)
12g.13866044C>GCA384054695GRIN2Bc.165G>C (p.Glu55Asp)
12g.13866044C>TCA478853900GRIN2Bc.165G>A (p.Glu55=)
12g.13866045T>ACA384054700GRIN2Bc.164A>T (p.Glu55Val)
12g.13866045T>CCA384054701GRIN2Bc.164A>G (p.Glu55Gly)
12g.13866045T>GCA384054703GRIN2Bc.164A>C (p.Glu55Ala)
12g.13866046C>ACA384054706GRIN2Bc.163G>T (p.Glu55Ter)
dbSNP
12g.13866046C=CA2017578244GRIN2Bc.163G= (p.Glu55=)
12g.13866046C>GCA384054708GRIN2Bc.163G>C (p.Glu55Gln)
12g.13866046C>TCA6461450GRIN2Bc.163G>A (p.Glu55Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
12g.13866047G>ACA6461451GRIN2Bc.162C>T (p.His54=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.13866047G>CCA384054713GRIN2Bc.162C>G (p.His54Gln)
dbSNP
12g.13866047G=CA2017578245GRIN2Bc.162C= (p.His54=)
12g.13866047G>TCA384054712GRIN2Bc.162C>A (p.His54Gln)
12g.13866048T>ACA384054714GRIN2Bc.161A>T (p.His54Leu)
12g.13866048T>CCA384054716GRIN2Bc.161A>G (p.His54Arg)
dbSNP
12g.13866048T>GCA384054718GRIN2Bc.161A>C (p.His54Pro)
12g.13866048T=CA2017578246GRIN2Bc.161A= (p.His54=)
12g.13866049G>ACA384054721GRIN2Bc.160C>T (p.His54Tyr)
dbSNP
12g.13866049G>CCA384054724GRIN2Bc.160C>G (p.His54Asp)
12g.13866049G>TCA384054726GRIN2Bc.160C>A (p.His54Asn)
12g.13866050G>ACA478853901GRIN2Bc.159C>T (p.Ala53=)
gnomAD v4
12g.13866050G>CCA478853902GRIN2Bc.159C>G (p.Ala53=)
12g.13866050G>TCA478853903GRIN2Bc.159C>A (p.Ala53=)
12g.13866051G>ACA384054732GRIN2Bc.158C>T (p.Ala53Val)
dbSNP gnomAD v4
12g.13866051G>CCA384054728GRIN2Bc.158C>G (p.Ala53Gly)
dbSNP gnomAD v2 gnomAD v4
12g.13866051G=CA2017578247GRIN2Bc.158C= (p.Ala53=)
12g.13866051G>TCA384054730GRIN2Bc.158C>A (p.Ala53Asp)
12g.13866052C>ACA384054734GRIN2Bc.157G>T (p.Ala53Ser)
ClinVar
12g.13866052C>GCA384054735GRIN2Bc.157G>C (p.Ala53Pro)
12g.13866052C>TCA384054737GRIN2Bc.157G>A (p.Ala53Thr)
COSMIC
12g.13866053A>CCA384054739GRIN2Bc.156T>G (p.Asp52Glu)
12g.13866053A>GCA478853904GRIN2Bc.156T>C (p.Asp52=)
12g.13866053A>TCA384054742GRIN2Bc.156T>A (p.Asp52Glu)
gnomAD v4
12g.13866054T>ACA384054749GRIN2Bc.155A>T (p.Asp52Val)
12g.13866054T>CCA384054745GRIN2Bc.155A>G (p.Asp52Gly)
12g.13866054T>GCA384054747GRIN2Bc.155A>C (p.Asp52Ala)
12g.13866055C>ACA384054752GRIN2Bc.154G>T (p.Asp52Tyr)
12g.13866055C>GCA384054754GRIN2Bc.154G>C (p.Asp52His)
12g.13866055C>TCA384054756GRIN2Bc.154G>A (p.Asp52Asn)
12g.13866056C>ACA384054757GRIN2Bc.153G>T (p.Lys51Asn)
12g.13866056C=CA2017578248GRIN2Bc.153G= (p.Lys51=)
12g.13866056C>GCA384054758GRIN2Bc.153G>C (p.Lys51Asn)
12g.13866056C>TCA16607183GRIN2Bc.153G>A (p.Lys51=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.13866057T>ACA384054761GRIN2Bc.152A>T (p.Lys51Met)
12g.13866057T>CCA384054764GRIN2Bc.152A>G (p.Lys51Arg)
12g.13866057T>GCA384054766GRIN2Bc.152A>C (p.Lys51Thr)
12g.13866058T>ACA384054770GRIN2Bc.151A>T (p.Lys51Ter)
dbSNP
12g.13866058T>CCA384054772GRIN2Bc.151A>G (p.Lys51Glu)
12g.13866058T>GCA384054774GRIN2Bc.151A>C (p.Lys51Gln)
12g.13866058T=CA2017578249GRIN2Bc.151A= (p.Lys51=)
12g.13866059G>ACA478853905GRIN2Bc.150C>T (p.Ile50=)
dbSNP
12g.13866059G>CCA384054777GRIN2Bc.150C>G (p.Ile50Met)
12g.13866059G=CA2017578250GRIN2Bc.150C= (p.Ile50=)
12g.13866059G>TCA6461452GRIN2Bc.150C>A (p.Ile50=)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.13866060A>CCA384054781GRIN2Bc.149T>G (p.Ile50Ser)
12g.13866060A>GCA384054790GRIN2Bc.149T>C (p.Ile50Thr)
12g.13866060A>TCA384054783GRIN2Bc.149T>A (p.Ile50Asn)
12g.13866061T>ACA384054794GRIN2Bc.148A>T (p.Ile50Phe)
12g.13866061T>CCA384054796GRIN2Bc.148A>G (p.Ile50Val)
12g.13866061T>GCA384054799GRIN2Bc.148A>C (p.Ile50Leu)
12g.13866062G>ACA478853906GRIN2Bc.147C>T (p.Ala49=)
dbSNP gnomAD v3 gnomAD v4
12g.13866062G>CCA478853907GRIN2Bc.147C>G (p.Ala49=)
12g.13866062G=CA2017578251GRIN2Bc.147C= (p.Ala49=)
12g.13866062G>TCA478853908GRIN2Bc.147C>A (p.Ala49=)
12g.13866063G>ACA384054802GRIN2Bc.146C>T (p.Ala49Val)
gnomAD v4
12g.13866063G>CCA384054804GRIN2Bc.146C>G (p.Ala49Gly)
12g.13866063G>TCA384054806GRIN2Bc.146C>A (p.Ala49Asp)
12g.13866064C>ACA384054809GRIN2Bc.145G>T (p.Ala49Ser)
12g.13866064C>GCA384054811GRIN2Bc.145G>C (p.Ala49Pro)
12g.13866064C>TCA384054814GRIN2Bc.145G>A (p.Ala49Thr)
12g.13866065C>ACA478853909GRIN2Bc.144G>T (p.Val48=)
12g.13866065C=CA2017578252GRIN2Bc.144G= (p.Val48=)
12g.13866065C>GCA478853910GRIN2Bc.144G>C (p.Val48=)
COSMIC
12g.13866065C>TCA6461453GRIN2Bc.144G>A (p.Val48=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
12g.13866066A>CCA384054818GRIN2Bc.143T>G (p.Val48Gly)
12g.13866066A>GCA384054821GRIN2Bc.143T>C (p.Val48Ala)
12g.13866066A>TCA384054823GRIN2Bc.143T>A (p.Val48Glu)
12g.13866067C>ACA384054826GRIN2Bc.142G>T (p.Val48Leu)
12g.13866067C=CA2017578253GRIN2Bc.142G= (p.Val48=)
12g.13866067C>GCA384054829GRIN2Bc.142G>C (p.Val48Leu)
12g.13866067C>TCA6461454GRIN2Bc.142G>A (p.Val48Met)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.13866068C>ACA384054830GRIN2Bc.141G>T (p.Glu47Asp)
12g.13866068C>GCA384054832GRIN2Bc.141G>C (p.Glu47Asp)
12g.13866068C>TCA478853911GRIN2Bc.141G>A (p.Glu47=)
12g.13866069T>ACA384054835GRIN2Bc.140A>T (p.Glu47Val)
12g.13866069T>CCA315044GRIN2Bc.140A>G (p.Glu47Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.13866069T>GCA384054839GRIN2Bc.140A>C (p.Glu47Ala)
12g.13866069T=CA2017578254GRIN2Bc.140A= (p.Glu47=)
12g.13866070C>ACA384054842GRIN2Bc.139G>T (p.Glu47Ter)
dbSNP
12g.13866070C=CA2017578255GRIN2Bc.139G= (p.Glu47=)
12g.13866070C>GCA384054844GRIN2Bc.139G>C (p.Glu47Gln)
12g.13866070C>TCA233148013GRIN2Bc.139G>A (p.Glu47Lys)
dbSNP gnomAD v4 COSMIC
12g.13866071G>ACA6461455GRIN2Bc.138C>T (p.Asp46=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.13866071G>CCA384054850GRIN2Bc.138C>G (p.Asp46Glu)
12g.13866071G=CA2017578256GRIN2Bc.138C= (p.Asp46=)
12g.13866071G>TCA384054853GRIN2Bc.138C>A (p.Asp46Glu)
gnomAD v4
12g.13866072T>ACA384054860GRIN2Bc.137A>T (p.Asp46Val)
12g.13866072T>CCA384054858GRIN2Bc.137A>G (p.Asp46Gly)
12g.13866072T>GCA384054856GRIN2Bc.137A>C (p.Asp46Ala)
12g.13866073C>ACA384054865GRIN2Bc.136G>T (p.Asp46Tyr)
12g.13866073C=CA2017578257GRIN2Bc.136G= (p.Asp46=)
12g.13866073C>GCA384054863GRIN2Bc.136G>C (p.Asp46His)
12g.13866073C>TCA6461456GRIN2Bc.136G>A (p.Asp46Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
12g.13866074G>ACA6461457GRIN2Bc.135C>T (p.Ser45=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.13866074G>CCA478853912GRIN2Bc.135C>G (p.Ser45=)
12g.13866074G=CA2017578258GRIN2Bc.135C= (p.Ser45=)
12g.13866074G>TCA478853913GRIN2Bc.135C>A (p.Ser45=)
12g.13866075G>ACA384054875GRIN2Bc.134C>T (p.Ser45Phe)
12g.13866075G>CCA384054873GRIN2Bc.134C>G (p.Ser45Cys)
12g.13866075G>TCA384054877GRIN2Bc.134C>A (p.Ser45Tyr)
12g.13866076A>CCA384054878GRIN2Bc.133T>G (p.Ser45Ala)
12g.13866076A>GCA384054880GRIN2Bc.133T>C (p.Ser45Pro)
12g.13866076A>TCA384054881GRIN2Bc.133T>A (p.Ser45Thr)
12g.13866077A>CCA478853914GRIN2Bc.132T>G (p.Thr44=)
12g.13866077A>GCA478853916GRIN2Bc.132T>C (p.Thr44=)
12g.13866077A>TCA478853915GRIN2Bc.132T>A (p.Thr44=)
12g.13866078G>ACA384054885GRIN2Bc.131C>T (p.Thr44Ile)
12g.13866078G>CCA384054886GRIN2Bc.131C>G (p.Thr44Ser)
12g.13866078G>TCA384054887GRIN2Bc.131C>A (p.Thr44Asn)
12g.13866079T>ACA384054890GRIN2Bc.130A>T (p.Thr44Ser)
12g.13866079T>CCA384054892GRIN2Bc.130A>G (p.Thr44Ala)
12g.13866079T>GCA384054894GRIN2Bc.130A>C (p.Thr44Pro)
gnomAD v4
12g.13866080G>ACA478853917GRIN2Bc.129C>T (p.Gly43=)
12g.13866080G>CCA478853918GRIN2Bc.129C>G (p.Gly43=)
12g.13866080G>TCA478853919GRIN2Bc.129C>A (p.Gly43=)
12g.13866081C>ACA384054897GRIN2Bc.128G>T (p.Gly43Val)
12g.13866081C>GCA384054898GRIN2Bc.128G>C (p.Gly43Ala)
12g.13866081C>TCA384054899GRIN2Bc.128G>A (p.Gly43Asp)
gnomAD v4
12g.13866082C>ACA384054906GRIN2Bc.127G>T (p.Gly43Cys)
COSMIC
12g.13866082C>GCA384054902GRIN2Bc.127G>C (p.Gly43Arg)
12g.13866082C>TCA384054905GRIN2Bc.127G>A (p.Gly43Ser)
COSMIC
12g.13866083C>ACA233148014GRIN2Bc.126G>T (p.Val42=)
dbSNP gnomAD v4
12g.13866083C=CA2017578259GRIN2Bc.126G= (p.Val42=)
12g.13866083C>GCA478853920GRIN2Bc.126G>C (p.Val42=)
12g.13866083C>TCA478853921GRIN2Bc.126G>A (p.Val42=)
12g.13866084A=CA2017578260GRIN2Bc.125T= (p.Val42=)
12g.13866084A>CCA384054908GRIN2Bc.125T>G (p.Val42Gly)
12g.13866084A>GCA315081GRIN2Bc.125T>C (p.Val42Ala)
ClinVar dbSNP gnomAD v3 gnomAD v4
12g.13866084A>TCA384054911GRIN2Bc.125T>A (p.Val42Glu)
12g.13866085C>ACA384054914GRIN2Bc.124G>T (p.Val42Leu)
12g.13866085C>GCA384054915GRIN2Bc.124G>C (p.Val42Leu)
12g.13866085C>TCA384054917GRIN2Bc.124G>A (p.Val42Met)
gnomAD v4
12g.13866086G>ACA478853922GRIN2Bc.123C>T (p.Leu41=)
ClinVar dbSNP gnomAD v4
12g.13866086G>CCA478853923GRIN2Bc.123C>G (p.Leu41=)
12g.13866086G>TCA478853924GRIN2Bc.123C>A (p.Leu41=)
12g.13866087A>CCA384054920GRIN2Bc.122T>G (p.Leu41Arg)
12g.13866087A>GCA384054921GRIN2Bc.122T>C (p.Leu41Pro)
12g.13866087A>TCA384054923GRIN2Bc.122T>A (p.Leu41His)
12g.13866088G>ACA384054926GRIN2Bc.121C>T (p.Leu41Phe)
12g.13866088G>CCA384054928GRIN2Bc.121C>G (p.Leu41Val)
12g.13866088G>TCA384054930GRIN2Bc.121C>A (p.Leu41Ile)
12g.13866089G>ACA478853925GRIN2Bc.120C>T (p.Ile40=)
12g.13866089G>CCA384054932GRIN2Bc.120C>G (p.Ile40Met)
12g.13866089G>TCA478853926GRIN2Bc.120C>A (p.Ile40=)
12g.13866090A>CCA384054939GRIN2Bc.119T>G (p.Ile40Ser)
gnomAD v4
12g.13866090A>GCA384054935GRIN2Bc.119T>C (p.Ile40Thr)
12g.13866090A>TCA384054937GRIN2Bc.119T>A (p.Ile40Asn)
12g.13866091T>ACA384054942GRIN2Bc.118A>T (p.Ile40Phe)
12g.13866091T>CCA384054944GRIN2Bc.118A>G (p.Ile40Val)
12g.13866091T>GCA384054947GRIN2Bc.118A>C (p.Ile40Leu)
12g.13866092G>ACA478853929GRIN2Bc.117C>T (p.Val39=)
12g.13866092G>CCA478853927GRIN2Bc.117C>G (p.Val39=)
12g.13866092G>TCA478853928GRIN2Bc.117C>A (p.Val39=)
gnomAD v4
12g.13866093A>CCA384054953GRIN2Bc.116T>G (p.Val39Gly)
12g.13866093A>GCA384054951GRIN2Bc.116T>C (p.Val39Ala)
dbSNP gnomAD v3 gnomAD v4
12g.13866093A>TCA384054950GRIN2Bc.116T>A (p.Val39Asp)
12g.13866094C>ACA384054957GRIN2Bc.115G>T (p.Val39Phe)
12g.13866094C>GCA384054959GRIN2Bc.115G>C (p.Val39Leu)
12g.13866094C>TCA384054960GRIN2Bc.115G>A (p.Val39Ile)
12g.13866095A=CA2017578261GRIN2Bc.114T= (p.Ala38=)
12g.13866095A>CCA478853930GRIN2Bc.114T>G (p.Ala38=)
12g.13866095A>GCA478853931GRIN2Bc.114T>C (p.Ala38=)
12g.13866095A>TCA478853932GRIN2Bc.114T>A (p.Ala38=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.13866096G>ACA384054967GRIN2Bc.113C>T (p.Ala38Val)
12g.13866096G>CCA384054969GRIN2Bc.113C>G (p.Ala38Gly)
COSMIC
12g.13866096G>TCA384054971GRIN2Bc.113C>A (p.Ala38Asp)
12g.13866097C>ACA384054973GRIN2Bc.112G>T (p.Ala38Ser)
12g.13866097C>GCA384054975GRIN2Bc.112G>C (p.Ala38Pro)
12g.13866097C>TCA384054974GRIN2Bc.112G>A (p.Ala38Thr)
12g.13866098A>CCA384054976GRIN2Bc.111T>G (p.Ile37Met)
12g.13866098A>GCA478853933GRIN2Bc.111T>C (p.Ile37=)
12g.13866098A>TCA478853934GRIN2Bc.111T>A (p.Ile37=)
12g.13866099A>CCA384054977GRIN2Bc.110T>G (p.Ile37Ser)
12g.13866099A>GCA384054978GRIN2Bc.110T>C (p.Ile37Thr)
12g.13866099A>TCA384054979GRIN2Bc.110T>A (p.Ile37Asn)
12g.13866100T>ACA384054980GRIN2Bc.109A>T (p.Ile37Phe)
12g.13866100T>CCA233148015GRIN2Bc.109A>G (p.Ile37Val)
dbSNP gnomAD v4
12g.13866100T>GCA384054981GRIN2Bc.109A>C (p.Ile37Leu)
12g.13866100T=CA2017578262GRIN2Bc.109A= (p.Ile37=)
12g.13866101G>ACA233148016GRIN2Bc.108C>T (p.Gly36=)
dbSNP
12g.13866101G>CCA478853935GRIN2Bc.108C>G (p.Gly36=)
12g.13866101G=CA2017578263GRIN2Bc.108C= (p.Gly36=)
12g.13866101G>TCA478853936GRIN2Bc.108C>A (p.Gly36=)
12g.13866102C>ACA384054982GRIN2Bc.107G>T (p.Gly36Val)
12g.13866102C>GCA384054983GRIN2Bc.107G>C (p.Gly36Ala)
12g.13866102C>TCA384054984GRIN2Bc.107G>A (p.Gly36Asp)
12g.13866103C>ACA384054987GRIN2Bc.106G>T (p.Gly36Cys)
c.106G>T
12g.13866103C>GCA384054986GRIN2Bc.106G>C (p.Gly36Arg)
c.106G>C
12g.13866103C>TCA384054985GRIN2Bc.106G>A (p.Gly36Ser)
c.106G>A
12g.13866104A>CCA384054988GRIN2Bc.105T>G (p.Ile35Met)
12g.13866104A>GCA478853937GRIN2Bc.105T>C (p.Ile35=)
gnomAD v4
12g.13866104A>TCA478853938GRIN2Bc.105T>A (p.Ile35=)
12g.13866105dupCA645595293GRIN2Bc.105dup (p.Gly36TrpfsTer23)
c.105dup
COSMIC
12g.13866105A=CA2017578264GRIN2Bc.104T= (p.Ile35=)
12g.13866105A>CCA384054990GRIN2Bc.104T>G (p.Ile35Ser)
12g.13866105A>GCA233148017GRIN2Bc.104T>C (p.Ile35Thr)
ClinVar dbSNP gnomAD v2 gnomAD v4
12g.13866105A>TCA384054989GRIN2Bc.104T>A (p.Ile35Asn)
ClinVar
12g.13866106T>ACA384054991GRIN2Bc.103A>T (p.Ile35Phe)
12g.13866106T>CCA6461458GRIN2Bc.103A>G (p.Ile35Val)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.13866106T>GCA384054992GRIN2Bc.103A>C (p.Ile35Leu)
12g.13866106T=CA2017578265GRIN2Bc.103A= (p.Ile35=)
12g.13866107G>ACA478853939GRIN2Bc.102C>T (p.Ser34=)
12g.13866107G>CCA384054993GRIN2Bc.102C>G (p.Ser34Arg)
12g.13866107G>TCA384054994GRIN2Bc.102C>A (p.Ser34Arg)
12g.13866107_13866108delCA645595294GRIN2Bc.101_102del (p.Ser34AsnfsTer24)
c.101_102del (p.Ser34AsnfsTer?)
COSMIC
12g.13866108C>ACA6461459GRIN2Bc.101G>T (p.Ser34Ile)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.13866108C=CA2017578266GRIN2Bc.101G= (p.Ser34=)
12g.13866108C>GCA384054995GRIN2Bc.101G>C (p.Ser34Thr)
ClinVar
12g.13866108C>TCA384054996GRIN2Bc.101G>A (p.Ser34Asn)
dbSNP gnomAD v4 COSMIC
12g.13866109T>ACA384054999GRIN2Bc.100A>T (p.Ser34Cys)
12g.13866109T>CCA384054998GRIN2Bc.100A>G (p.Ser34Gly)
12g.13866109T>GCA384054997GRIN2Bc.100A>C (p.Ser34Arg)
12g.13866109T=CA2017578267GRIN2Bc.100A= (p.Ser34=)
12g.13866109dupCA2560228041GRIN2Bc.100dup (p.Ser34LysfsTer25)
c.100dup (p.Ser34LysfsTer?)
12g.13866109_13866126delCA2617757589GRIN2Bc.83_100del (p.Ser28_Ser34delinsCys)
gnomAD v4
12g.13866110G>ACA478853940GRIN2Bc.99C>T (p.Pro33=)
dbSNP gnomAD v2 gnomAD v4
12g.13866110G>CCA478853942GRIN2Bc.99C>G (p.Pro33=)
gnomAD v4
12g.13866110G=CA2017578268GRIN2Bc.99C= (p.Pro33=)
12g.13866110G>TCA6461460GRIN2Bc.99C>A (p.Pro33=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.13866116dupCA130434GRIN2Bc.99dup (p.Ser34GlnfsTer25)
c.99dup (p.Ser34GlnfsTer?)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
12g.13866116delCA478853941GRIN2Bc.99del (p.Ser34AlafsTer?)
ClinVar gnomAD v4 COSMIC
12g.13866110_13866111insCCA478853943GRIN2Bc.98_99insG (p.Ser34GlnfsTer25)
c.98_99insG (p.Ser34GlnfsTer?)
12g.13866111G>ACA384055000GRIN2Bc.98C>T (p.Pro33Leu)
COSMIC
12g.13866111G>CCA384055001GRIN2Bc.98C>G (p.Pro33Arg)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.13866111G=CA2017578269GRIN2Bc.98C= (p.Pro33=)
12g.13866111G>TCA384055002GRIN2Bc.98C>A (p.Pro33His)
12g.13866112G>ACA384055003GRIN2Bc.97C>T (p.Pro33Ser)
gnomAD v4
12g.13866112G>CCA384055004GRIN2Bc.97C>G (p.Pro33Ala)
12g.13866112G>TCA384055005GRIN2Bc.97C>A (p.Pro33Thr)
12g.13866113G>ACA478853944GRIN2Bc.96C>T (p.Pro32=)
ClinVar dbSNP
12g.13866113G>CCA478853945GRIN2Bc.96C>G (p.Pro32=)
12g.13866113G=CA2017578270GRIN2Bc.96C= (p.Pro32=)
12g.13866113G>TCA6461461GRIN2Bc.96C>A (p.Pro32=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.13866114G>ACA384055006GRIN2Bc.95C>T (p.Pro32Leu)
12g.13866114G>CCA384055007GRIN2Bc.95C>G (p.Pro32Arg)
12g.13866114G>TCA384055008GRIN2Bc.95C>A (p.Pro32His)
ClinVar gnomAD v4
12g.13866115G>ACA384055010GRIN2Bc.94C>T (p.Pro32Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
12g.13866115G>CCA384055011GRIN2Bc.94C>G (p.Pro32Ala)
dbSNP gnomAD v3 gnomAD v4 COSMIC
12g.13866115G=CA2017578271GRIN2Bc.94C= (p.Pro32=)
12g.13866115G>TCA384055009GRIN2Bc.94C>A (p.Pro32Thr)
ClinVar dbSNP gnomAD v2 gnomAD v4
12g.13866116G>ACA6461462GRIN2Bc.93C>T (p.Ser31=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.13866116G>CCA384055012GRIN2Bc.93C>G (p.Ser31Arg)
12g.13866116G=CA2017578272GRIN2Bc.93C= (p.Ser31=)
12g.13866116G>TCA384055013GRIN2Bc.93C>A (p.Ser31Arg)
gnomAD v4
12g.13866117C>ACA384055014GRIN2Bc.92G>T (p.Ser31Ile)
12g.13866117C=CA2017578273GRIN2Bc.92G= (p.Ser31=)
12g.13866117C>GCA384055015GRIN2Bc.92G>C (p.Ser31Thr)
ClinVar dbSNP gnomAD v4
12g.13866117C>TCA6461463GRIN2Bc.92G>A (p.Ser31Asn)
dbSNP ExAC gnomAD v2 gnomAD v4

Number of alleles fetched