Chr Mutation (hg38) CAid Gene Transcript Linkouts
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
12g.13866118T>ACA384055016GRIN2Bc.91A>T (p.Ser31Cys)
12g.13866118T>CCA384055017GRIN2Bc.91A>G (p.Ser31Gly)
12g.13866118T>GCA384055018GRIN2Bc.91A>C (p.Ser31Arg)
12g.13866119C>ACA384055019GRIN2Bc.90G>T (p.Lys30Asn)
12g.13866119C=CA2017578274GRIN2Bc.90G= (p.Lys30=)
12g.13866119C>GCA384055020GRIN2Bc.90G>C (p.Lys30Asn)
12g.13866119C>TCA233148018GRIN2Bc.90G>A (p.Lys30=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.13866120T>ACA384055022GRIN2Bc.89A>T (p.Lys30Met)
12g.13866120T>CCA384055023GRIN2Bc.89A>G (p.Lys30Arg)
12g.13866120T>GCA384055021GRIN2Bc.89A>C (p.Lys30Thr)
12g.13866121T>ACA384055024GRIN2Bc.88A>T (p.Lys30Ter)
dbSNP
12g.13866121T>CCA384055025GRIN2Bc.88A>G (p.Lys30Glu)
gnomAD v4
12g.13866121T>GCA384055026GRIN2Bc.88A>C (p.Lys30Gln)
12g.13866121T=CA2017578275GRIN2Bc.88A= (p.Lys30=)
12g.13866122C>ACA384055027GRIN2Bc.87G>T (p.Gln29His)
12g.13866122C>GCA384055028GRIN2Bc.87G>C (p.Gln29His)
12g.13866122C>TCA478853946GRIN2Bc.87G>A (p.Gln29=)
12g.13866123T>ACA384055031GRIN2Bc.86A>T (p.Gln29Leu)
12g.13866123T>CCA384055029GRIN2Bc.86A>G (p.Gln29Arg)
gnomAD v4
12g.13866123T>GCA384055030GRIN2Bc.86A>C (p.Gln29Pro)
12g.13866124G>ACA384055032GRIN2Bc.85C>T (p.Gln29Ter)
dbSNP
12g.13866124G>CCA384055033GRIN2Bc.85C>G (p.Gln29Glu)
12g.13866124G=CA2017578276GRIN2Bc.85C= (p.Gln29=)
12g.13866124G>TCA384055034GRIN2Bc.85C>A (p.Gln29Lys)
12g.13866125A>CCA478853947GRIN2Bc.84T>G (p.Ser28=)
12g.13866125A>GCA478853948GRIN2Bc.84T>C (p.Ser28=)
12g.13866125A>TCA478853949GRIN2Bc.84T>A (p.Ser28=)
12g.13866126G>ACA384055035GRIN2Bc.83C>T (p.Ser28Phe)
12g.13866126G>CCA384055036GRIN2Bc.83C>G (p.Ser28Cys)
12g.13866126G>TCA384055037GRIN2Bc.83C>A (p.Ser28Tyr)
12g.13866127A>CCA384055039GRIN2Bc.82T>G (p.Ser28Ala)
12g.13866127A>GCA384055040GRIN2Bc.82T>C (p.Ser28Pro)
12g.13866127A>TCA384055038GRIN2Bc.82T>A (p.Ser28Thr)
12g.13866128A>CCA478853950GRIN2Bc.81T>G (p.Arg27=)
12g.13866128A>GCA478853952GRIN2Bc.81T>C (p.Arg27=)
12g.13866128A>TCA478853951GRIN2Bc.81T>A (p.Arg27=)
12g.13866129C>ACA6461465GRIN2Bc.80G>T (p.Arg27Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.13866129C=CA2017578277GRIN2Bc.80G= (p.Arg27=)
12g.13866129C>GCA384055041GRIN2Bc.80G>C (p.Arg27Pro)
12g.13866129C>TCA6461464GRIN2Bc.80G>A (p.Arg27His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.13866130G>ACA384055042GRIN2Bc.79C>T (p.Arg27Cys)
dbSNP gnomAD v2 COSMIC
12g.13866130G>CCA384055043GRIN2Bc.79C>G (p.Arg27Gly)
12g.13866130G=CA2017578278GRIN2Bc.79C= (p.Arg27=)
12g.13866130G>TCA384055044GRIN2Bc.79C>A (p.Arg27Ser)
12g.13866131A>CCA478853955GRIN2Bc.78T>G (p.Ala26=)
12g.13866131A>GCA478853953GRIN2Bc.78T>C (p.Ala26=)
gnomAD v4
12g.13866131A>TCA478853954GRIN2Bc.78T>A (p.Ala26=)
12g.13866132G>ACA384055046GRIN2Bc.77C>T (p.Ala26Val)
ClinVar gnomAD v4
12g.13866132G>CCA233148019GRIN2Bc.77C>G (p.Ala26Gly)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.13866132G=CA2017578279GRIN2Bc.77C= (p.Ala26=)
12g.13866132G>TCA384055045GRIN2Bc.77C>A (p.Ala26Asp)
12g.13866133C>ACA384055047GRIN2Bc.76G>T (p.Ala26Ser)
12g.13866133C=CA2017578280GRIN2Bc.76G= (p.Ala26=)
12g.13866133C>GCA384055048GRIN2Bc.76G>C (p.Ala26Pro)
12g.13866133C>TCA6461466GRIN2Bc.76G>A (p.Ala26Thr)
ClinVar dbSNP ExAC gnomAD v4
12g.13866134T>ACA384055049GRIN2Bc.75A>T (p.Arg25Ser)
12g.13866134T>CCA478853956GRIN2Bc.75A>G (p.Arg25=)
12g.13866134T>GCA233148020GRIN2Bc.75A>C (p.Arg25Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4
12g.13866134T=CA2017578281GRIN2Bc.75A= (p.Arg25=)
12g.13866135C>ACA384055052GRIN2Bc.74G>T (p.Arg25Ile)
12g.13866135C>GCA384055050GRIN2Bc.74G>C (p.Arg25Thr)
12g.13866135C>TCA384055051GRIN2Bc.74G>A (p.Arg25Lys)
12g.13866136T>ACA384055053GRIN2Bc.73A>T (p.Arg25Ter)
12g.13866136T>CCA384055054GRIN2Bc.73A>G (p.Arg25Gly)
12g.13866136T>GCA478853957GRIN2Bc.73A>C (p.Arg25=)
12g.13866137G>ACA233148021GRIN2Bc.72C>T (p.Ser24=)
ClinVar dbSNP
12g.13866137G>CCA384055055GRIN2Bc.72C>G (p.Ser24Arg)
12g.13866137G=CA2017578282GRIN2Bc.72C= (p.Ser24=)
12g.13866137G>TCA384055056GRIN2Bc.72C>A (p.Ser24Arg)
gnomAD v4
12g.13866138C>ACA384055059GRIN2Bc.71G>T (p.Ser24Ile)
12g.13866138C=CA2017578283GRIN2Bc.71G= (p.Ser24=)
12g.13866138C>GCA384055058GRIN2Bc.71G>C (p.Ser24Thr)
12g.13866138C>TCA384055057GRIN2Bc.71G>A (p.Ser24Asn)
dbSNP gnomAD v3 gnomAD v4
12g.13866139T>ACA384055060GRIN2Bc.70A>T (p.Ser24Cys)
12g.13866139T>CCA384055061GRIN2Bc.70A>G (p.Ser24Gly)
12g.13866139T>GCA384055062GRIN2Bc.70A>C (p.Ser24Arg)
12g.13866140G>ACA478853958GRIN2Bc.69C>T (p.Gly23=)
12g.13866140G>CCA478853960GRIN2Bc.69C>G (p.Gly23=)
dbSNP gnomAD v4
12g.13866140G=CA2017578284GRIN2Bc.69C= (p.Gly23=)
12g.13866140G>TCA478853959GRIN2Bc.69C>A (p.Gly23=)
12g.13866141C>ACA384055063GRIN2Bc.68G>T (p.Gly23Val)
12g.13866141C>GCA384055064GRIN2Bc.68G>C (p.Gly23Ala)
12g.13866141C>TCA384055065GRIN2Bc.68G>A (p.Gly23Asp)
12g.13866142C>ACA384055066GRIN2Bc.67G>T (p.Gly23Cys)
12g.13866142C>GCA384055068GRIN2Bc.67G>C (p.Gly23Arg)
12g.13866142C>TCA384055067GRIN2Bc.67G>A (p.Gly23Ser)
12g.13866143T>ACA478853961GRIN2Bc.66A>T (p.Ser22=)
ClinVar dbSNP
12g.13866143T>CCA478853962GRIN2Bc.66A>G (p.Ser22=)
ClinVar
12g.13866143T>GCA478853963GRIN2Bc.66A>C (p.Ser22=)
12g.13866143T=CA2017578285GRIN2Bc.66A= (p.Ser22=)
12g.13866144G>ACA384055069GRIN2Bc.65C>T (p.Ser22Leu)
12g.13866144G>CCA384055070GRIN2Bc.65C>G (p.Ser22Ter)
12g.13866144G>TCA384055071GRIN2Bc.65C>A (p.Ser22Ter)
12g.13866145A>CCA384055072GRIN2Bc.64T>G (p.Ser22Ala)
gnomAD v4
12g.13866145A>GCA384055073GRIN2Bc.64T>C (p.Ser22Pro)
12g.13866145A>TCA384055074GRIN2Bc.64T>A (p.Ser22Thr)
12g.13866145_13866146delinsCACA2573053638GRIN2Bc.63_64delinsTG (p.Ser22Ala)
ClinVar dbSNP
12g.13866146C>ACA478853964GRIN2Bc.63G>T (p.Val21=)
gnomAD v4
12g.13866146C=CA2017578286GRIN2Bc.63G= (p.Val21=)
12g.13866146C>GCA6461467GRIN2Bc.63G>C (p.Val21=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.13866146C>TCA478853965GRIN2Bc.63G>A (p.Val21=)
12g.13866147A>CCA384055075GRIN2Bc.62T>G (p.Val21Gly)
12g.13866147A>GCA384055077GRIN2Bc.62T>C (p.Val21Ala)
12g.13866147A>TCA384055076GRIN2Bc.62T>A (p.Val21Glu)
gnomAD v4
12g.13866148C>ACA384055078GRIN2Bc.61G>T (p.Val21Leu)
COSMIC
12g.13866148C=CA2017578287GRIN2Bc.61G= (p.Val21=)
12g.13866148C>GCA384055079GRIN2Bc.61G>C (p.Val21Leu)
12g.13866148C>TCA315040GRIN2Bc.61G>A (p.Val21Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.13866149G>ACA6461468GRIN2Bc.60C>T (p.Ala20=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.13866149G>CCA478853966GRIN2Bc.60C>G (p.Ala20=)
12g.13866149G=CA2017578288GRIN2Bc.60C= (p.Ala20=)
12g.13866149G>TCA478853967GRIN2Bc.60C>A (p.Ala20=)
gnomAD v4
12g.13866150G>ACA384055080GRIN2Bc.59C>T (p.Ala20Val)
dbSNP gnomAD v4
12g.13866150G>CCA384055082GRIN2Bc.59C>G (p.Ala20Gly)
12g.13866150G=CA2017578289GRIN2Bc.59C= (p.Ala20=)
12g.13866150G>TCA384055081GRIN2Bc.59C>A (p.Ala20Asp)
12g.13866151C>ACA384055083GRIN2Bc.58G>T (p.Ala20Ser)
12g.13866151C>GCA384055084GRIN2Bc.58G>C (p.Ala20Pro)
12g.13866151C>TCA384055085GRIN2Bc.58G>A (p.Ala20Thr)
12g.13866152C>ACA478853968GRIN2Bc.57G>T (p.Leu19=)
12g.13866152C>GCA478853970GRIN2Bc.57G>C (p.Leu19=)
12g.13866152C>TCA478853969GRIN2Bc.57G>A (p.Leu19=)
12g.13866153A>CCA384055086GRIN2Bc.56T>G (p.Leu19Arg)
12g.13866153A>GCA384055087GRIN2Bc.56T>C (p.Leu19Pro)
12g.13866153A>TCA384055088GRIN2Bc.56T>A (p.Leu19Gln)
12g.13866154G>ACA478853971GRIN2Bc.55C>T (p.Leu19=)
12g.13866154G>CCA384055089GRIN2Bc.55C>G (p.Leu19Val)
12g.13866154G>TCA384055090GRIN2Bc.55C>A (p.Leu19Met)
12g.13866155G>ACA478853974GRIN2Bc.54C>T (p.Val18=)
12g.13866155G>CCA478853972GRIN2Bc.54C>G (p.Val18=)
12g.13866155G>TCA478853973GRIN2Bc.54C>A (p.Val18=)
12g.13866156A>CCA384055091GRIN2Bc.53T>G (p.Val18Gly)
12g.13866156A>GCA384055092GRIN2Bc.53T>C (p.Val18Ala)
12g.13866156A>TCA384055093GRIN2Bc.53T>A (p.Val18Asp)
12g.13866157C>ACA384055094GRIN2Bc.52G>T (p.Val18Phe)
12g.13866157C=CA2017578290GRIN2Bc.52G= (p.Val18=)
12g.13866157C>GCA384055095GRIN2Bc.52G>C (p.Val18Leu)
12g.13866157C>TCA315038GRIN2Bc.52G>A (p.Val18Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched