Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.13753440C>ACA384053219GRIN2Bc.887G>T (p.Gly296Val)
12g.13753440C>GCA384053220GRIN2Bc.887G>C (p.Gly296Ala)
12g.13753440C>TCA384053221GRIN2Bc.887G>A (p.Gly296Glu)
12g.13753441C>ACA384053223GRIN2Bc.886G>T (p.Gly296Ter)
dbSNP
12g.13753441C=CA2017525830GRIN2Bc.886G= (p.Gly296=)
12g.13753441C>GCA384053224GRIN2Bc.886G>C (p.Gly296Arg)
12g.13753441C>TCA384053222GRIN2Bc.886G>A (p.Gly296Arg)
COSMIC
12g.13753442A>CCA384053226GRIN2Bc.885T>G (p.Asp295Glu)
12g.13753442A>GCA478853496GRIN2Bc.885T>C (p.Asp295=)
12g.13753442A>TCA384053225GRIN2Bc.885T>A (p.Asp295Glu)
12g.13753443T>ACA384053227GRIN2Bc.884A>T (p.Asp295Val)
12g.13753443T>CCA384053228GRIN2Bc.884A>G (p.Asp295Gly)
12g.13753443T>GCA384053229GRIN2Bc.884A>C (p.Asp295Ala)
12g.13753444C>ACA384053230GRIN2Bc.883G>T (p.Asp295Tyr)
12g.13753444C>GCA384053231GRIN2Bc.883G>C (p.Asp295His)
12g.13753444C>TCA384053232GRIN2Bc.883G>A (p.Asp295Asn)
12g.13753445T>ACA384053233GRIN2Bc.882A>T (p.Arg294Ser)
12g.13753445T>CCA478853497GRIN2Bc.882A>G (p.Arg294=)
gnomAD v4
12g.13753445T>GCA384053234GRIN2Bc.882A>C (p.Arg294Ser)
12g.13753446C>ACA384053235GRIN2Bc.881G>T (p.Arg294Ile)
12g.13753446C>GCA384053236GRIN2Bc.881G>C (p.Arg294Thr)
12g.13753446C>TCA384053237GRIN2Bc.881G>A (p.Arg294Lys)
12g.13753447T>ACA384053238GRIN2Bc.880A>T (p.Arg294Ter)
dbSNP
12g.13753447T>CCA384053239GRIN2Bc.880A>G (p.Arg294Gly)
12g.13753447T>GCA478853498GRIN2Bc.880A>C (p.Arg294=)
12g.13753447T=CA2017525831GRIN2Bc.880A= (p.Arg294=)
12g.13753448C>ACA478853499GRIN2Bc.879G>T (p.Val293=)
12g.13753448C>GCA478853500GRIN2Bc.879G>C (p.Val293=)
12g.13753448C>TCA478853501GRIN2Bc.879G>A (p.Val293=)
12g.13753449A>CCA384053240GRIN2Bc.878T>G (p.Val293Gly)
12g.13753449A>GCA384053242GRIN2Bc.878T>C (p.Val293Ala)
12g.13753449A>TCA384053241GRIN2Bc.878T>A (p.Val293Glu)
12g.13753450C>ACA384053243GRIN2Bc.877G>T (p.Val293Leu)
gnomAD v4
12g.13753450C=CA2017525832GRIN2Bc.877G= (p.Val293=)
12g.13753450C>GCA384053244GRIN2Bc.877G>C (p.Val293Leu)
12g.13753450C>TCA384053245GRIN2Bc.877G>A (p.Val293Met)
ClinVar dbSNP
12g.13753451T>ACA384053246GRIN2Bc.876A>T (p.Arg292Ser)
12g.13753451T>CCA10577450GRIN2Bc.876A>G (p.Arg292=)
ClinVar dbSNP gnomAD v4
12g.13753451T>GCA384053247GRIN2Bc.876A>C (p.Arg292Ser)
12g.13753451T=CA2017525833GRIN2Bc.876A= (p.Arg292=)
12g.13753452C>ACA384053248GRIN2Bc.875G>T (p.Arg292Ile)
12g.13753452C>GCA384053249GRIN2Bc.875G>C (p.Arg292Thr)
12g.13753452C>TCA384053250GRIN2Bc.875G>A (p.Arg292Lys)
12g.13753453T>ACA384053251GRIN2Bc.874A>T (p.Arg292Ter)
dbSNP
12g.13753453T>CCA384053252GRIN2Bc.874A>G (p.Arg292Gly)
12g.13753453T>GCA6461354GRIN2Bc.874A>C (p.Arg292=)
dbSNP ExAC gnomAD v2
12g.13753453T=CA2017525834GRIN2Bc.874A= (p.Arg292=)
12g.13753454G>ACA478853503GRIN2Bc.873C>T (p.Ala291=)
12g.13753454G>CCA6461355GRIN2Bc.873C>G (p.Ala291=)
dbSNP ExAC gnomAD v2
12g.13753454G=CA2017525835GRIN2Bc.873C= (p.Ala291=)
12g.13753454G>TCA478853502GRIN2Bc.873C>A (p.Ala291=)
gnomAD v4
12g.13753455G>ACA384053255GRIN2Bc.872C>T (p.Ala291Val)
dbSNP gnomAD v2
12g.13753455G>CCA384053253GRIN2Bc.872C>G (p.Ala291Gly)
12g.13753455G=CA2017525836GRIN2Bc.872C= (p.Ala291=)
12g.13753455G>TCA384053254GRIN2Bc.872C>A (p.Ala291Asp)
12g.13753456C>ACA384053256GRIN2Bc.871G>T (p.Ala291Ser)
gnomAD v4
12g.13753456C=CA2017525837GRIN2Bc.871G= (p.Ala291=)
12g.13753456C>GCA384053257GRIN2Bc.871G>C (p.Ala291Pro)
12g.13753456C>TCA384053258GRIN2Bc.871G>A (p.Ala291Thr)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.13753457G>ACA153052GRIN2Bc.870C>T (p.Pro290=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.13753457G>CCA478853504GRIN2Bc.870C>G (p.Pro290=)
12g.13753457G=CA2017525838GRIN2Bc.870C= (p.Pro290=)
12g.13753457G>TCA6461356GRIN2Bc.870C>A (p.Pro290=)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.13753458G>ACA384053259GRIN2Bc.869C>T (p.Pro290Leu)
12g.13753458G>CCA384053260GRIN2Bc.869C>G (p.Pro290Arg)
12g.13753458G>TCA384053261GRIN2Bc.869C>A (p.Pro290His)
12g.13753459G>ACA384053262GRIN2Bc.868C>T (p.Pro290Ser)
ClinVar dbSNP
12g.13753459G>CCA384053263GRIN2Bc.868C>G (p.Pro290Ala)
12g.13753459G=CA2017525839GRIN2Bc.868C= (p.Pro290=)
12g.13753459G>TCA384053264GRIN2Bc.868C>A (p.Pro290Thr)
12g.13753460G>ACA478853506GRIN2Bc.867C>T (p.Leu289=)
12g.13753460G>CCA478853507GRIN2Bc.867C>G (p.Leu289=)
12g.13753460G>TCA478853508GRIN2Bc.867C>A (p.Leu289=)
12g.13753461A>CCA384053266GRIN2Bc.866T>G (p.Leu289Arg)
12g.13753461A>GCA384053267GRIN2Bc.866T>C (p.Leu289Pro)
12g.13753461A>TCA384053265GRIN2Bc.866T>A (p.Leu289His)
12g.13753462G>ACA384053268GRIN2Bc.865C>T (p.Leu289Phe)
COSMIC
12g.13753462G>CCA384053269GRIN2Bc.865C>G (p.Leu289Val)
12g.13753462G>TCA384053270GRIN2Bc.865C>A (p.Leu289Ile)
12g.13753463G>ACA478853509GRIN2Bc.864C>T (p.Gly288=)
12g.13753463G>CCA478853510GRIN2Bc.864C>G (p.Gly288=)
12g.13753463G>TCA478853511GRIN2Bc.864C>A (p.Gly288=)
12g.13753464C>ACA384053271GRIN2Bc.863G>T (p.Gly288Val)
12g.13753464C>GCA384053272GRIN2Bc.863G>C (p.Gly288Ala)
12g.13753464C>TCA384053273GRIN2Bc.863G>A (p.Gly288Asp)
12g.13753465C>ACA384053274GRIN2Bc.862G>T (p.Gly288Cys)
12g.13753465C>GCA384053276GRIN2Bc.862G>C (p.Gly288Arg)
ClinVar
12g.13753465C>TCA384053275GRIN2Bc.862G>A (p.Gly288Ser)
12g.13753466A>CCA384053277GRIN2Bc.861T>G (p.Tyr287Ter)
12g.13753466A>GCA478853514GRIN2Bc.861T>C (p.Tyr287=)
ClinVar gnomAD v4
12g.13753466A>TCA384053278GRIN2Bc.861T>A (p.Tyr287Ter)
12g.13753467T>ACA384053279GRIN2Bc.860A>T (p.Tyr287Phe)
12g.13753467T>CCA384053280GRIN2Bc.860A>G (p.Tyr287Cys)
12g.13753467T>GCA384053281GRIN2Bc.860A>C (p.Tyr287Ser)
12g.13753468A>CCA384053283GRIN2Bc.859T>G (p.Tyr287Asp)
12g.13753468A>GCA384053284GRIN2Bc.859T>C (p.Tyr287His)
12g.13753468A>TCA384053282GRIN2Bc.859T>A (p.Tyr287Asn)
12g.13753469G>ACA478853516GRIN2Bc.858C>T (p.Asp286=)
dbSNP gnomAD v2 gnomAD v4
12g.13753469G>CCA384053285GRIN2Bc.858C>G (p.Asp286Glu)
12g.13753469G=CA2017525840GRIN2Bc.858C= (p.Asp286=)
12g.13753469G>TCA384053286GRIN2Bc.858C>A (p.Asp286Glu)
12g.13753470T>ACA384053287GRIN2Bc.857A>T (p.Asp286Val)
dbSNP
12g.13753470T>CCA384053288GRIN2Bc.857A>G (p.Asp286Gly)
ClinVar
12g.13753470T>GCA384053289GRIN2Bc.857A>C (p.Asp286Ala)
12g.13753470T=CA2017525841GRIN2Bc.857A= (p.Asp286=)
12g.13753471C>ACA384053290GRIN2Bc.856G>T (p.Asp286Tyr)
12g.13753471C>GCA384053291GRIN2Bc.856G>C (p.Asp286His)
ClinVar
12g.13753471C>TCA384053292GRIN2Bc.856G>A (p.Asp286Asn)
12g.13753472C>ACA384053293GRIN2Bc.855G>T (p.Trp285Cys)
12g.13753472C=CA2017525842GRIN2Bc.855G= (p.Trp285=)
12g.13753472C>GCA384053294GRIN2Bc.855G>C (p.Trp285Cys)
12g.13753472C>TCA384053295GRIN2Bc.855G>A (p.Trp285Ter)
dbSNP
12g.13753473C>ACA384053296GRIN2Bc.854G>T (p.Trp285Leu)
12g.13753473C=CA2017525843GRIN2Bc.854G= (p.Trp285=)
12g.13753473C>GCA384053297GRIN2Bc.854G>C (p.Trp285Ser)
12g.13753473C>TCA384053298GRIN2Bc.854G>A (p.Trp285Ter)
dbSNP
12g.13753474A>CCA384053301GRIN2Bc.853T>G (p.Trp285Gly)
12g.13753474A>GCA384053300GRIN2Bc.853T>C (p.Trp285Arg)
12g.13753474A>TCA384053299GRIN2Bc.853T>A (p.Trp285Arg)
12g.13753475T>ACA384053302GRIN2Bc.852A>T (p.Glu284Asp)
12g.13753475T>CCA478853523GRIN2Bc.852A>G (p.Glu284=)
12g.13753475T>GCA384053303GRIN2Bc.852A>C (p.Glu284Asp)
12g.13753476T>ACA384053304GRIN2Bc.851A>T (p.Glu284Val)
12g.13753476T>CCA384053305GRIN2Bc.851A>G (p.Glu284Gly)
12g.13753476T>GCA233115790GRIN2Bc.851A>C (p.Glu284Ala)
dbSNP
12g.13753476T=CA2017525844GRIN2Bc.851A= (p.Glu284=)
12g.13753477C>ACA384053306GRIN2Bc.850G>T (p.Glu284Ter)
12g.13753477C>GCA384053307GRIN2Bc.850G>C (p.Glu284Gln)
12g.13753477C>TCA384053308GRIN2Bc.850G>A (p.Glu284Lys)
COSMIC
12g.13753478A>CCA384053309GRIN2Bc.849T>G (p.Asp283Glu)
12g.13753478A>GCA478853525GRIN2Bc.849T>C (p.Asp283=)
gnomAD v4
12g.13753478A>TCA384053310GRIN2Bc.849T>A (p.Asp283Glu)
12g.13753479T>ACA384053311GRIN2Bc.848A>T (p.Asp283Val)
12g.13753479T>CCA384053312GRIN2Bc.848A>G (p.Asp283Gly)
12g.13753479T>GCA384053313GRIN2Bc.848A>C (p.Asp283Ala)
12g.13753480C>ACA384053316GRIN2Bc.847G>T (p.Asp283Tyr)
12g.13753480C>GCA384053315GRIN2Bc.847G>C (p.Asp283His)
12g.13753480C>TCA384053314GRIN2Bc.847G>A (p.Asp283Asn)
COSMIC
12g.13753481A=CA2017525845GRIN2Bc.846T= (p.Tyr282=)
12g.13753481A>CCA384053318GRIN2Bc.846T>G (p.Tyr282Ter)
12g.13753481A>GCA478853529GRIN2Bc.846T>C (p.Tyr282=)
ClinVar dbSNP gnomAD v2 gnomAD v4
12g.13753481A>TCA384053317GRIN2Bc.846T>A (p.Tyr282Ter)
12g.13753482T>ACA384053319GRIN2Bc.845A>T (p.Tyr282Phe)
12g.13753482T>CCA384053320GRIN2Bc.845A>G (p.Tyr282Cys)
ClinVar
12g.13753482T>GCA384053321GRIN2Bc.845A>C (p.Tyr282Ser)
12g.13753483A>CCA384053322GRIN2Bc.844T>G (p.Tyr282Asp)
12g.13753483A>GCA384053323GRIN2Bc.844T>C (p.Tyr282His)
12g.13753483A>TCA384053324GRIN2Bc.844T>A (p.Tyr282Asn)
12g.13753484T>ACA478853531GRIN2Bc.843A>T (p.Ser281=)
12g.13753484T>CCA233115795GRIN2Bc.843A>G (p.Ser281=)
ClinVar dbSNP gnomAD v2 gnomAD v4
12g.13753484T>GCA478853532GRIN2Bc.843A>C (p.Ser281=)
12g.13753484T=CA2017525846GRIN2Bc.843A= (p.Ser281=)
12g.13753485G>ACA233115798GRIN2Bc.842C>T (p.Ser281Leu)
dbSNP
12g.13753485G>CCA384053325GRIN2Bc.842C>G (p.Ser281Ter)
12g.13753485G=CA2017525847GRIN2Bc.842C= (p.Ser281=)
12g.13753485G>TCA384053326GRIN2Bc.842C>A (p.Ser281Ter)
12g.13753486A=CA2017525848GRIN2Bc.841T= (p.Ser281=)
12g.13753486A>CCA384053327GRIN2Bc.841T>G (p.Ser281Ala)
12g.13753486A>GCA384053328GRIN2Bc.841T>C (p.Ser281Pro)
12g.13753486A>TCA384053329GRIN2Bc.841T>A (p.Ser281Thr)
ClinVar dbSNP
12g.13753487T>ACA478853534GRIN2Bc.840A>T (p.Val280=)
12g.13753487T>CCA6461357GRIN2Bc.840A>G (p.Val280=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
12g.13753487T>GCA478853535GRIN2Bc.840A>C (p.Val280=)
12g.13753487T=CA2017525849GRIN2Bc.840A= (p.Val280=)
12g.13753487_13753489delinsTACCA2017525850GRIN2Bc.838_840delinsGTA (p.Val280=)
12g.13753488A>CCA384053330GRIN2Bc.839T>G (p.Val280Gly)
12g.13753488A>GCA384053331GRIN2Bc.839T>C (p.Val280Ala)
12g.13753488A>TCA384053332GRIN2Bc.839T>A (p.Val280Glu)
12g.13753489_13753490delCA658658122GRIN2Bc.838_839del (p.Val280IlefsTer3)
ClinVar dbSNP
12g.13753489C>ACA384053333GRIN2Bc.838G>T (p.Val280Leu)
12g.13753489C=CA2017525851GRIN2Bc.838G= (p.Val280=)
12g.13753489C>GCA384053334GRIN2Bc.838G>C (p.Val280Leu)
12g.13753489C>TCA6461358GRIN2Bc.838G>A (p.Val280Ile)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.13753490A>CCA478853538GRIN2Bc.837T>G (p.Ser279=)
12g.13753490A>GCA478853539GRIN2Bc.837T>C (p.Ser279=)
12g.13753490A>TCA478853540GRIN2Bc.837T>A (p.Ser279=)
12g.13753491G>ACA384053335GRIN2Bc.836C>T (p.Ser279Phe)
12g.13753491G>CCA384053336GRIN2Bc.836C>G (p.Ser279Cys)
12g.13753491G>TCA384053337GRIN2Bc.836C>A (p.Ser279Tyr)
12g.13753492A>CCA384053338GRIN2Bc.835T>G (p.Ser279Ala)
12g.13753492A>GCA384053339GRIN2Bc.835T>C (p.Ser279Pro)
12g.13753492A>TCA384053340GRIN2Bc.835T>A (p.Ser279Thr)
12g.13753493G>ACA478853544GRIN2Bc.834C>T (p.Ile278=)
12g.13753493G>CCA384053341GRIN2Bc.834C>G (p.Ile278Met)
12g.13753493G=CA2017525852GRIN2Bc.834C= (p.Ile278=)
12g.13753493G>TCA6461359GRIN2Bc.834C>A (p.Ile278=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.13753494A>CCA384053343GRIN2Bc.833T>G (p.Ile278Ser)
12g.13753494A>GCA384053344GRIN2Bc.833T>C (p.Ile278Thr)
12g.13753494A>TCA384053342GRIN2Bc.833T>A (p.Ile278Asn)
12g.13753495T>ACA384053345GRIN2Bc.832A>T (p.Ile278Phe)
12g.13753495T>CCA384053347GRIN2Bc.832A>G (p.Ile278Val)
12g.13753495T>GCA384053346GRIN2Bc.832A>C (p.Ile278Leu)
12g.13753496G>ACA478853546GRIN2Bc.831C>T (p.Leu277=)
ClinVar gnomAD v4
12g.13753496G>CCA478853547GRIN2Bc.831C>G (p.Leu277=)
gnomAD v4
12g.13753496G>TCA478853548GRIN2Bc.831C>A (p.Leu277=)
12g.13753497A>CCA384053348GRIN2Bc.830T>G (p.Leu277Arg)
12g.13753497A>GCA384053349GRIN2Bc.830T>C (p.Leu277Pro)
12g.13753497A>TCA384053350GRIN2Bc.830T>A (p.Leu277His)
12g.13753498G>ACA384053351GRIN2Bc.829C>T (p.Leu277Phe)
COSMIC
12g.13753498G>CCA384053352GRIN2Bc.829C>G (p.Leu277Val)
dbSNP
12g.13753498G=CA2017525853GRIN2Bc.829C= (p.Leu277=)
12g.13753498G>TCA384053353GRIN2Bc.829C>A (p.Leu277Ile)
12g.13753499C>ACA478853552GRIN2Bc.828G>T (p.Gly276=)
gnomAD v4
12g.13753499C>GCA478853554GRIN2Bc.828G>C (p.Gly276=)
12g.13753499C>TCA478853553GRIN2Bc.828G>A (p.Gly276=)
gnomAD v4
12g.13753500C>ACA384053354GRIN2Bc.827G>T (p.Gly276Val)
12g.13753500C>GCA384053355GRIN2Bc.827G>C (p.Gly276Ala)
12g.13753500C>TCA384053356GRIN2Bc.827G>A (p.Gly276Glu)
12g.13753501C>ACA384053357GRIN2Bc.826G>T (p.Gly276Trp)
12g.13753501C>GCA384053358GRIN2Bc.826G>C (p.Gly276Arg)
12g.13753501C>TCA384053359GRIN2Bc.826G>A (p.Gly276Arg)
12g.13753502A=CA2017525854GRIN2Bc.825T= (p.Thr275=)
12g.13753502A>CCA478853559GRIN2Bc.825T>G (p.Thr275=)
12g.13753502A>GCA478853556GRIN2Bc.825T>C (p.Thr275=)
dbSNP gnomAD v2 gnomAD v4
12g.13753502A>TCA478853558GRIN2Bc.825T>A (p.Thr275=)
12g.13753503G>ACA384053362GRIN2Bc.824C>T (p.Thr275Ile)
12g.13753503G>CCA384053360GRIN2Bc.824C>G (p.Thr275Ser)
12g.13753503G>TCA384053361GRIN2Bc.824C>A (p.Thr275Asn)
gnomAD v4
12g.13753506_13753526delCA2695216106GRIN2Bc.804_824del (p.Val269_Thr275del)
12g.13753504T>ACA384053363GRIN2Bc.823A>T (p.Thr275Ser)
gnomAD v4
12g.13753504T>CCA384053364GRIN2Bc.823A>G (p.Thr275Ala)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.13753504T>GCA384053365GRIN2Bc.823A>C (p.Thr275Pro)
12g.13753504T=CA2017525855GRIN2Bc.823A= (p.Thr275=)
12g.13753505G>ACA478853563GRIN2Bc.822C>T (p.Pro274=)
ClinVar dbSNP
12g.13753505G>CCA478853564GRIN2Bc.822C>G (p.Pro274=)
12g.13753505G=CA2017525856GRIN2Bc.822C= (p.Pro274=)
12g.13753505G>TCA478853565GRIN2Bc.822C>A (p.Pro274=)
12g.13753506G>ACA384053366GRIN2Bc.821C>T (p.Pro274Leu)
dbSNP gnomAD v3 gnomAD v4
12g.13753506G>CCA384053367GRIN2Bc.821C>G (p.Pro274Arg)
12g.13753506G=CA2017525857GRIN2Bc.821C= (p.Pro274=)
12g.13753506G>TCA384053368GRIN2Bc.821C>A (p.Pro274His)
12g.13753507G>ACA233115804GRIN2Bc.820C>T (p.Pro274Ser)
dbSNP COSMIC
12g.13753507G>CCA384053369GRIN2Bc.820C>G (p.Pro274Ala)
12g.13753507G=CA2017525858GRIN2Bc.820C= (p.Pro274=)
12g.13753507G>TCA384053370GRIN2Bc.820C>A (p.Pro274Thr)
12g.13753508G>ACA478853567GRIN2Bc.819C>T (p.Phe273=)
12g.13753508G>CCA6461360GRIN2Bc.819C>G (p.Phe273Leu)
dbSNP ExAC gnomAD v2
12g.13753508G=CA2017525859GRIN2Bc.819C= (p.Phe273=)
12g.13753508G>TCA384053371GRIN2Bc.819C>A (p.Phe273Leu)
12g.13753509A>CCA384053374GRIN2Bc.818T>G (p.Phe273Cys)
12g.13753509A>GCA384053373GRIN2Bc.818T>C (p.Phe273Ser)
12g.13753509A>TCA384053372GRIN2Bc.818T>A (p.Phe273Tyr)
12g.13753510A>CCA384053375GRIN2Bc.817T>G (p.Phe273Val)
ClinVar
12g.13753510A>GCA384053376GRIN2Bc.817T>C (p.Phe273Leu)
12g.13753510A>TCA384053377GRIN2Bc.817T>A (p.Phe273Ile)
12g.13753511C>ACA6461361GRIN2Bc.816G>T (p.Glu272Asp)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.13753511C=CA2017525860GRIN2Bc.816G= (p.Glu272=)
12g.13753511C>GCA384053378GRIN2Bc.816G>C (p.Glu272Asp)
12g.13753511C>TCA478853571GRIN2Bc.816G>A (p.Glu272=)
gnomAD v4
12g.13753512T>ACA384053379GRIN2Bc.815A>T (p.Glu272Val)
12g.13753512T>CCA384053380GRIN2Bc.815A>G (p.Glu272Gly)
12g.13753512T>GCA384053381GRIN2Bc.815A>C (p.Glu272Ala)
12g.13753513C>ACA384053382GRIN2Bc.814G>T (p.Glu272Ter)
dbSNP
12g.13753513C=CA2017525861GRIN2Bc.814G= (p.Glu272=)
12g.13753513C>GCA384053383GRIN2Bc.814G>C (p.Glu272Gln)
12g.13753513C>TCA384053384GRIN2Bc.814G>A (p.Glu272Lys)
COSMIC
12g.13753514C>ACA478853574GRIN2Bc.813G>T (p.Ala271=)
gnomAD v4
12g.13753514C=CA2017525862GRIN2Bc.813G= (p.Ala271=)
12g.13753514C>GCA478853573GRIN2Bc.813G>C (p.Ala271=)
12g.13753514C>TCA233115820GRIN2Bc.813G>A (p.Ala271=)
ClinVar dbSNP gnomAD v2 gnomAD v4
12g.13753515G>ACA6461362GRIN2Bc.812C>T (p.Ala271Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.13753515G>CCA384053385GRIN2Bc.812C>G (p.Ala271Gly)
12g.13753515G=CA2017525863GRIN2Bc.812C= (p.Ala271=)
12g.13753515G>TCA315032GRIN2Bc.812C>A (p.Ala271Glu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.13753516C>ACA384053386GRIN2Bc.811G>T (p.Ala271Ser)
gnomAD v3 gnomAD v4
12g.13753516C=CA2017525864GRIN2Bc.811G= (p.Ala271=)
12g.13753516C>GCA384053387GRIN2Bc.811G>C (p.Ala271Pro)
12g.13753516C>TCA384053388GRIN2Bc.811G>A (p.Ala271Thr)
ClinVar dbSNP gnomAD v4
12g.13753517A>CCA478853577GRIN2Bc.810T>G (p.Pro270=)
12g.13753517A>GCA478853578GRIN2Bc.810T>C (p.Pro270=)
12g.13753517A>TCA478853579GRIN2Bc.810T>A (p.Pro270=)
12g.13753518G>ACA384053389GRIN2Bc.809C>T (p.Pro270Leu)
COSMIC
12g.13753518G>CCA384053390GRIN2Bc.809C>G (p.Pro270Arg)
12g.13753518G>TCA384053391GRIN2Bc.809C>A (p.Pro270His)
dbSNP COSMIC
12g.13753519G>ACA384053392GRIN2Bc.808C>T (p.Pro270Ser)
12g.13753519G>CCA384053394GRIN2Bc.808C>G (p.Pro270Ala)
12g.13753519G>TCA384053393GRIN2Bc.808C>A (p.Pro270Thr)
12g.13753520C>ACA478853584GRIN2Bc.807G>T (p.Val269=)
12g.13753520C=CA2017525865GRIN2Bc.807G= (p.Val269=)
12g.13753520C>GCA478853585GRIN2Bc.807G>C (p.Val269=)
12g.13753520C>TCA233115830GRIN2Bc.807G>A (p.Val269=)
ClinVar dbSNP gnomAD v4
12g.13753521A>CCA384053395GRIN2Bc.806T>G (p.Val269Gly)
12g.13753521A>GCA384053401GRIN2Bc.806T>C (p.Val269Ala)
12g.13753521A>TCA384053403GRIN2Bc.806T>A (p.Val269Glu)
gnomAD v4
12g.13753522C>ACA384053405GRIN2Bc.805G>T (p.Val269Leu)
COSMIC
12g.13753522C=CA2017525867GRIN2Bc.805G= (p.Val269=)
12g.13753522C>GCA384053408GRIN2Bc.805G>C (p.Val269Leu)
ClinVar dbSNP gnomAD v2 gnomAD v4
12g.13753522C>TCA384053406GRIN2Bc.805G>A (p.Val269Met)
gnomAD v4 COSMIC
12g.13753522_13753524delinsCTGCA2017525866GRIN2Bc.803_805delinsCAG (p.Thr268=)
12g.13753523T>ACA478853589GRIN2Bc.804A>T (p.Thr268=)
12g.13753523T>CCA6461363GRIN2Bc.804A>G (p.Thr268=)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.13753523T>GCA478853590GRIN2Bc.804A>C (p.Thr268=)
12g.13753523T=CA2017525868GRIN2Bc.804A= (p.Thr268=)
12g.13753526_13753527delCA16609334GRIN2Bc.803_804del (p.Thr268SerfsTer15)
ClinVar dbSNP
12g.13753524G>ACA384053414GRIN2Bc.803C>T (p.Thr268Ile)
12g.13753524G>CCA384053411GRIN2Bc.803C>G (p.Thr268Arg)
12g.13753524G>TCA384053412GRIN2Bc.803C>A (p.Thr268Lys)
gnomAD v4
12g.13753525T>ACA384053416GRIN2Bc.802A>T (p.Thr268Ser)
12g.13753525T>CCA384053417GRIN2Bc.802A>G (p.Thr268Ala)
12g.13753525T>GCA233115839GRIN2Bc.802A>C (p.Thr268Pro)
ClinVar dbSNP gnomAD v2
12g.13753525T=CA2017525869GRIN2Bc.802A= (p.Thr268=)
12g.13753526G>ACA478853593GRIN2Bc.801C>T (p.Asp267=)
12g.13753526G>CCA384053422GRIN2Bc.801C>G (p.Asp267Glu)
12g.13753526G>TCA384053424GRIN2Bc.801C>A (p.Asp267Glu)
12g.13753527T>ACA384053426GRIN2Bc.800A>T (p.Asp267Val)
12g.13753527T>CCA384053427GRIN2Bc.800A>G (p.Asp267Gly)
12g.13753527T>GCA384053430GRIN2Bc.800A>C (p.Asp267Ala)
12g.13753528C>ACA384053431GRIN2Bc.799G>T (p.Asp267Tyr)
12g.13753528C>GCA384053433GRIN2Bc.799G>C (p.Asp267His)
12g.13753528C>TCA384053434GRIN2Bc.799G>A (p.Asp267Asn)
12g.13753529T>ACA478853594GRIN2Bc.798A>T (p.Thr266=)
12g.13753529T>CCA478853595GRIN2Bc.798A>G (p.Thr266=)
12g.13753529T>GCA478853596GRIN2Bc.798A>C (p.Thr266=)
12g.13753530G>ACA6461364GRIN2Bc.797C>T (p.Thr266Ile)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.13753530G>CCA384053438GRIN2Bc.797C>G (p.Thr266Arg)
12g.13753530G=CA2017525870GRIN2Bc.797C= (p.Thr266=)
12g.13753530G>TCA384053435GRIN2Bc.797C>A (p.Thr266Lys)
12g.13753531T>ACA384053440GRIN2Bc.796A>T (p.Thr266Ser)
12g.13753531T>CCA233115845GRIN2Bc.796A>G (p.Thr266Ala)
dbSNP
12g.13753531T>GCA384053441GRIN2Bc.796A>C (p.Thr266Pro)
12g.13753531T=CA2017525871GRIN2Bc.796A= (p.Thr266=)
12g.13753532A>CCA384053442GRIN2Bc.795T>G (p.Asp265Glu)
12g.13753532A>GCA478853598GRIN2Bc.795T>C (p.Asp265=)
12g.13753532A>TCA384053444GRIN2Bc.795T>A (p.Asp265Glu)
12g.13753533T>ACA384053446GRIN2Bc.794A>T (p.Asp265Val)
12g.13753533T>CCA384053448GRIN2Bc.794A>G (p.Asp265Gly)
12g.13753533T>GCA384053452GRIN2Bc.794A>C (p.Asp265Ala)
12g.13753534C>ACA384053454GRIN2Bc.793G>T (p.Asp265Tyr)
12g.13753534C>GCA384053455GRIN2Bc.793G>C (p.Asp265His)
12g.13753534C>TCA384053456GRIN2Bc.793G>A (p.Asp265Asn)
COSMIC
12g.13753535C>ACA478853600GRIN2Bc.792G>T (p.Gly264=)
COSMIC
12g.13753535C=CA2017525872GRIN2Bc.792G= (p.Gly264=)
12g.13753535C>GCA478853602GRIN2Bc.792G>C (p.Gly264=)
12g.13753535C>TCA478853601GRIN2Bc.792G>A (p.Gly264=)
dbSNP gnomAD v2 gnomAD v4
12g.13753536C>ACA384053459GRIN2Bc.791G>T (p.Gly264Val)
12g.13753536C>GCA384053458GRIN2Bc.791G>C (p.Gly264Ala)
12g.13753536C>TCA384053457GRIN2Bc.791G>A (p.Gly264Glu)
COSMIC
12g.13753537C>ACA384053463GRIN2Bc.790G>T (p.Gly264Trp)
12g.13753537C>GCA384053460GRIN2Bc.790G>C (p.Gly264Arg)
12g.13753537C>TCA384053462GRIN2Bc.790G>A (p.Gly264Arg)
12g.13753538T>ACA478853603GRIN2Bc.789A>T (p.Ala263=)
12g.13753538T>CCA478853604GRIN2Bc.789A>G (p.Ala263=)
12g.13753538T>GCA6461365GRIN2Bc.789A>C (p.Ala263=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.13753538T=CA2017525873GRIN2Bc.789A= (p.Ala263=)
12g.13753539G>ACA384053466GRIN2Bc.788C>T (p.Ala263Val)
12g.13753539G>CCA384053468GRIN2Bc.788C>G (p.Ala263Gly)
12g.13753539G>TCA384053471GRIN2Bc.788C>A (p.Ala263Glu)
12g.13753540C>ACA384053473GRIN2Bc.787G>T (p.Ala263Ser)
dbSNP
12g.13753540C=CA2017525874GRIN2Bc.787G= (p.Ala263=)
12g.13753540C>GCA384053475GRIN2Bc.787G>C (p.Ala263Pro)
12g.13753540C>TCA384053477GRIN2Bc.787G>A (p.Ala263Thr)

Number of alleles fetched