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.9763297C>ACA394705582GRIN2Ac.4247G>T (p.Ser1416Ile)
c.*58G>T (n.*58G>T)
n.3497G>T
c.3776G>T (p.Ser1259Ile)
c.*1617G>T (n.*1617G>T)
c.3836G>T (p.Ser1279Ile)
n.3543G>T
c.4088G>T (p.Ser1363Ile)
c.3989G>T (p.Ser1330Ile)
c.4403G>T (p.Ser1468Ile)
ClinVar dbSNP gnomAD v3 gnomAD v4
16g.9763297C=CA2206692651GRIN2Ac.4247G= (p.Ser1416=)
c.*58G= (n.*58G=)
n.3497G=
c.3776G= (p.Ser1259=)
c.*1617G= (n.*1617G=)
c.3836G= (p.Ser1279=)
n.3543G=
c.4088G= (p.Ser1363=)
c.3989G= (p.Ser1330=)
c.4403G= (p.Ser1468=)
16g.9763297C>GCA394705584GRIN2Ac.4247G>C (p.Ser1416Thr)
c.*58G>C (n.*58G>C)
n.3497G>C
c.3776G>C (p.Ser1259Thr)
c.*1617G>C (n.*1617G>C)
c.3836G>C (p.Ser1279Thr)
n.3543G>C
c.4088G>C (p.Ser1363Thr)
c.3989G>C (p.Ser1330Thr)
c.4403G>C (p.Ser1468Thr)
ClinVar dbSNP gnomAD v4
16g.9763297C>TCA7896189GRIN2Ac.4247G>A (p.Ser1416Asn)
c.*58G>A (n.*58G>A)
n.3497G>A
c.3776G>A (p.Ser1259Asn)
c.*1617G>A (n.*1617G>A)
c.3836G>A (p.Ser1279Asn)
n.3543G>A
c.4088G>A (p.Ser1363Asn)
c.3989G>A (p.Ser1330Asn)
c.4403G>A (p.Ser1468Asn)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.9763298T>ACA394705588GRIN2Ac.4246A>T (p.Ser1416Cys)
c.*57A>T (n.*57A>T)
n.3496A>T
c.3775A>T (p.Ser1259Cys)
c.*1616A>T (n.*1616A>T)
c.3835A>T (p.Ser1279Cys)
n.3542A>T
c.4087A>T (p.Ser1363Cys)
c.3988A>T (p.Ser1330Cys)
c.4402A>T (p.Ser1468Cys)
16g.9763298T>CCA394705590GRIN2Ac.4246A>G (p.Ser1416Gly)
c.*57A>G (n.*57A>G)
n.3496A>G
c.3775A>G (p.Ser1259Gly)
c.*1616A>G (n.*1616A>G)
c.3835A>G (p.Ser1279Gly)
n.3542A>G
c.4087A>G (p.Ser1363Gly)
c.3988A>G (p.Ser1330Gly)
c.4402A>G (p.Ser1468Gly)
dbSNP
16g.9763298T>GCA394705591GRIN2Ac.4246A>C (p.Ser1416Arg)
c.*57A>C (n.*57A>C)
n.3496A>C
c.3775A>C (p.Ser1259Arg)
c.*1616A>C (n.*1616A>C)
c.3835A>C (p.Ser1279Arg)
n.3542A>C
c.4087A>C (p.Ser1363Arg)
c.3988A>C (p.Ser1330Arg)
c.4402A>C (p.Ser1468Arg)
dbSNP
16g.9763299G>ACA493692559GRIN2Ac.4245C>T (p.Asp1415=)
c.*56C>T (n.*56C>T)
n.3495C>T
c.3774C>T (p.Asp1258=)
c.*1615C>T (n.*1615C>T)
c.3834C>T (p.Asp1278=)
n.3541C>T
c.4086C>T (p.Asp1362=)
c.3987C>T (p.Asp1329=)
c.4401C>T (p.Asp1467=)
dbSNP COSMIC
16g.9763299G>CCA394705593GRIN2Ac.4245C>G (p.Asp1415Glu)
c.*56C>G (n.*56C>G)
n.3495C>G
c.3774C>G (p.Asp1258Glu)
c.*1615C>G (n.*1615C>G)
c.3834C>G (p.Asp1278Glu)
n.3541C>G
c.4086C>G (p.Asp1362Glu)
c.3987C>G (p.Asp1329Glu)
c.4401C>G (p.Asp1467Glu)
dbSNP
16g.9763299G=CA2206692652GRIN2Ac.4245C= (p.Asp1415=)
c.*56C= (n.*56C=)
n.3495C=
c.3774C= (p.Asp1258=)
c.*1615C= (n.*1615C=)
c.3834C= (p.Asp1278=)
n.3541C=
c.4086C= (p.Asp1362=)
c.3987C= (p.Asp1329=)
c.4401C= (p.Asp1467=)
16g.9763299G>TCA7896190GRIN2Ac.4245C>A (p.Asp1415Glu)
c.*56C>A (n.*56C>A)
n.3495C>A
c.3774C>A (p.Asp1258Glu)
c.*1615C>A (n.*1615C>A)
c.3834C>A (p.Asp1278Glu)
n.3541C>A
c.4086C>A (p.Asp1362Glu)
c.3987C>A (p.Asp1329Glu)
c.4401C>A (p.Asp1467Glu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
16g.9763300T>ACA394705598GRIN2Ac.4244A>T (p.Asp1415Val)
c.*55A>T (n.*55A>T)
n.3494A>T
c.3773A>T (p.Asp1258Val)
c.*1614A>T (n.*1614A>T)
c.3833A>T (p.Asp1278Val)
n.3540A>T
c.4085A>T (p.Asp1362Val)
c.3986A>T (p.Asp1329Val)
c.4400A>T (p.Asp1467Val)
16g.9763300T>CCA394705600GRIN2Ac.4244A>G (p.Asp1415Gly)
c.*55A>G (n.*55A>G)
n.3494A>G
c.3773A>G (p.Asp1258Gly)
c.*1614A>G (n.*1614A>G)
c.3833A>G (p.Asp1278Gly)
n.3540A>G
c.4085A>G (p.Asp1362Gly)
c.3986A>G (p.Asp1329Gly)
c.4400A>G (p.Asp1467Gly)
16g.9763300T>GCA394705596GRIN2Ac.4244A>C (p.Asp1415Ala)
c.*55A>C (n.*55A>C)
n.3494A>C
c.3773A>C (p.Asp1258Ala)
c.*1614A>C (n.*1614A>C)
c.3833A>C (p.Asp1278Ala)
n.3540A>C
c.4085A>C (p.Asp1362Ala)
c.3986A>C (p.Asp1329Ala)
c.4400A>C (p.Asp1467Ala)
16g.9763301C>ACA394705602GRIN2Ac.4243G>T (p.Asp1415Tyr)
c.*54G>T (n.*54G>T)
n.3493G>T
c.3772G>T (p.Asp1258Tyr)
c.*1613G>T (n.*1613G>T)
c.3832G>T (p.Asp1278Tyr)
n.3539G>T
c.4084G>T (p.Asp1362Tyr)
c.3985G>T (p.Asp1329Tyr)
c.4399G>T (p.Asp1467Tyr)
dbSNP
16g.9763301C>GCA394705604GRIN2Ac.4243G>C (p.Asp1415His)
c.*54G>C (n.*54G>C)
n.3493G>C
c.3772G>C (p.Asp1258His)
c.*1613G>C (n.*1613G>C)
c.3832G>C (p.Asp1278His)
n.3539G>C
c.4084G>C (p.Asp1362His)
c.3985G>C (p.Asp1329His)
c.4399G>C (p.Asp1467His)
16g.9763301C>TCA394705606GRIN2Ac.4243G>A (p.Asp1415Asn)
c.*54G>A (n.*54G>A)
n.3493G>A
c.3772G>A (p.Asp1258Asn)
c.*1613G>A (n.*1613G>A)
c.3832G>A (p.Asp1278Asn)
n.3539G>A
c.4084G>A (p.Asp1362Asn)
c.3985G>A (p.Asp1329Asn)
c.4399G>A (p.Asp1467Asn)
dbSNP gnomAD v4
16g.9763302C>ACA394705608GRIN2Ac.4242G>T (p.Arg1414Ser)
c.*53G>T (n.*53G>T)
n.3492G>T
c.3771G>T (p.Arg1257Ser)
c.*1612G>T (n.*1612G>T)
c.3831G>T (p.Arg1277Ser)
n.3538G>T
c.4083G>T (p.Arg1361Ser)
c.3984G>T (p.Arg1328Ser)
c.4398G>T (p.Arg1466Ser)
dbSNP
16g.9763302C>GCA394705610GRIN2Ac.4242G>C (p.Arg1414Ser)
c.*53G>C (n.*53G>C)
n.3492G>C
c.3771G>C (p.Arg1257Ser)
c.*1612G>C (n.*1612G>C)
c.3831G>C (p.Arg1277Ser)
n.3538G>C
c.4083G>C (p.Arg1361Ser)
c.3984G>C (p.Arg1328Ser)
c.4398G>C (p.Arg1466Ser)
16g.9763302C>TCA493692565GRIN2Ac.4242G>A (p.Arg1414=)
c.*53G>A (n.*53G>A)
n.3492G>A
c.3771G>A (p.Arg1257=)
c.*1612G>A (n.*1612G>A)
c.3831G>A (p.Arg1277=)
n.3538G>A
c.4083G>A (p.Arg1361=)
c.3984G>A (p.Arg1328=)
c.4398G>A (p.Arg1466=)
dbSNP
16g.9763303C>ACA394705617GRIN2Ac.4241G>T (p.Arg1414Met)
c.*52G>T (n.*52G>T)
n.3491G>T
c.3770G>T (p.Arg1257Met)
c.*1611G>T (n.*1611G>T)
c.3830G>T (p.Arg1277Met)
n.3537G>T
c.4082G>T (p.Arg1361Met)
c.3983G>T (p.Arg1328Met)
c.4397G>T (p.Arg1466Met)
dbSNP
16g.9763303C=CA2206692653GRIN2Ac.4241G= (p.Arg1414=)
c.*52G= (n.*52G=)
n.3491G=
c.3770G= (p.Arg1257=)
c.*1611G= (n.*1611G=)
c.3830G= (p.Arg1277=)
n.3537G=
c.4082G= (p.Arg1361=)
c.3983G= (p.Arg1328=)
c.4397G= (p.Arg1466=)
16g.9763303C>GCA394705613GRIN2Ac.4241G>C (p.Arg1414Thr)
c.*52G>C (n.*52G>C)
n.3491G>C
c.3770G>C (p.Arg1257Thr)
c.*1611G>C (n.*1611G>C)
c.3830G>C (p.Arg1277Thr)
n.3537G>C
c.4082G>C (p.Arg1361Thr)
c.3983G>C (p.Arg1328Thr)
c.4397G>C (p.Arg1466Thr)
dbSNP gnomAD v4
16g.9763303C>TCA394705615GRIN2Ac.4241G>A (p.Arg1414Lys)
c.*52G>A (n.*52G>A)
n.3491G>A
c.3770G>A (p.Arg1257Lys)
c.*1611G>A (n.*1611G>A)
c.3830G>A (p.Arg1277Lys)
n.3537G>A
c.4082G>A (p.Arg1361Lys)
c.3983G>A (p.Arg1328Lys)
c.4397G>A (p.Arg1466Lys)
dbSNP
16g.9763304T>ACA394705619GRIN2Ac.4240A>T (p.Arg1414Trp)
c.*51A>T (n.*51A>T)
n.3490A>T
c.3769A>T (p.Arg1257Trp)
c.*1610A>T (n.*1610A>T)
c.3829A>T (p.Arg1277Trp)
n.3536A>T
c.4081A>T (p.Arg1361Trp)
c.3982A>T (p.Arg1328Trp)
c.4396A>T (p.Arg1466Trp)
16g.9763304T>CCA277535897GRIN2Ac.4240A>G (p.Arg1414Gly)
c.*51A>G (n.*51A>G)
n.3490A>G
c.3769A>G (p.Arg1257Gly)
c.*1610A>G (n.*1610A>G)
c.3829A>G (p.Arg1277Gly)
n.3536A>G
c.4081A>G (p.Arg1361Gly)
c.3982A>G (p.Arg1328Gly)
c.4396A>G (p.Arg1466Gly)
dbSNP gnomAD v2 gnomAD v4
16g.9763304T>GCA493692566GRIN2Ac.4240A>C (p.Arg1414=)
c.*51A>C (n.*51A>C)
n.3490A>C
c.3769A>C (p.Arg1257=)
c.*1610A>C (n.*1610A>C)
c.3829A>C (p.Arg1277=)
n.3536A>C
c.4081A>C (p.Arg1361=)
c.3982A>C (p.Arg1328=)
c.4396A>C (p.Arg1466=)
16g.9763304T=CA2206692654GRIN2Ac.4240A= (p.Arg1414=)
c.*51A= (n.*51A=)
n.3490A=
c.3769A= (p.Arg1257=)
c.*1610A= (n.*1610A=)
c.3829A= (p.Arg1277=)
n.3536A=
c.4081A= (p.Arg1361=)
c.3982A= (p.Arg1328=)
c.4396A= (p.Arg1466=)
16g.9763305G>ACA493692567GRIN2Ac.4239C>T (p.Ser1413=)
c.*50C>T (n.*50C>T)
n.3489C>T
c.3768C>T (p.Ser1256=)
c.*1609C>T (n.*1609C>T)
c.3828C>T (p.Ser1276=)
n.3535C>T
c.4080C>T (p.Ser1360=)
c.3981C>T (p.Ser1327=)
c.4395C>T (p.Ser1465=)
dbSNP
16g.9763305G>CCA493692569GRIN2Ac.4239C>G (p.Ser1413=)
c.*50C>G (n.*50C>G)
n.3489C>G
c.3768C>G (p.Ser1256=)
c.*1609C>G (n.*1609C>G)
c.3828C>G (p.Ser1276=)
n.3535C>G
c.4080C>G (p.Ser1360=)
c.3981C>G (p.Ser1327=)
c.4395C>G (p.Ser1465=)
dbSNP
16g.9763305G>TCA493692570GRIN2Ac.4239C>A (p.Ser1413=)
c.*50C>A (n.*50C>A)
n.3489C>A
c.3768C>A (p.Ser1256=)
c.*1609C>A (n.*1609C>A)
c.3828C>A (p.Ser1276=)
n.3535C>A
c.4080C>A (p.Ser1360=)
c.3981C>A (p.Ser1327=)
c.4395C>A (p.Ser1465=)
dbSNP
16g.9763306G>ACA394705623GRIN2Ac.4238C>T (p.Ser1413Phe)
c.*49C>T (n.*49C>T)
n.3488C>T
c.3767C>T (p.Ser1256Phe)
c.*1608C>T (n.*1608C>T)
c.3827C>T (p.Ser1276Phe)
n.3534C>T
c.4079C>T (p.Ser1360Phe)
c.3980C>T (p.Ser1327Phe)
c.4394C>T (p.Ser1465Phe)
dbSNP gnomAD v4
16g.9763306G>CCA394705625GRIN2Ac.4238C>G (p.Ser1413Cys)
c.*49C>G (n.*49C>G)
n.3488C>G
c.3767C>G (p.Ser1256Cys)
c.*1608C>G (n.*1608C>G)
c.3827C>G (p.Ser1276Cys)
n.3534C>G
c.4079C>G (p.Ser1360Cys)
c.3980C>G (p.Ser1327Cys)
c.4394C>G (p.Ser1465Cys)
dbSNP
16g.9763306G>TCA394705627GRIN2Ac.4238C>A (p.Ser1413Tyr)
c.*49C>A (n.*49C>A)
n.3488C>A
c.3767C>A (p.Ser1256Tyr)
c.*1608C>A (n.*1608C>A)
c.3827C>A (p.Ser1276Tyr)
n.3534C>A
c.4079C>A (p.Ser1360Tyr)
c.3980C>A (p.Ser1327Tyr)
c.4394C>A (p.Ser1465Tyr)
dbSNP
16g.9763307A>CCA394705633GRIN2Ac.4237T>G (p.Ser1413Ala)
c.*48T>G (n.*48T>G)
n.3487T>G
c.3766T>G (p.Ser1256Ala)
c.*1607T>G (n.*1607T>G)
c.3826T>G (p.Ser1276Ala)
n.3533T>G
c.4078T>G (p.Ser1360Ala)
c.3979T>G (p.Ser1327Ala)
c.4393T>G (p.Ser1465Ala)
16g.9763307A>GCA394705631GRIN2Ac.4237T>C (p.Ser1413Pro)
c.*48T>C (n.*48T>C)
n.3487T>C
c.3766T>C (p.Ser1256Pro)
c.*1607T>C (n.*1607T>C)
c.3826T>C (p.Ser1276Pro)
n.3533T>C
c.4078T>C (p.Ser1360Pro)
c.3979T>C (p.Ser1327Pro)
c.4393T>C (p.Ser1465Pro)
dbSNP
16g.9763307A>TCA394705629GRIN2Ac.4237T>A (p.Ser1413Thr)
c.*48T>A (n.*48T>A)
n.3487T>A
c.3766T>A (p.Ser1256Thr)
c.*1607T>A (n.*1607T>A)
c.3826T>A (p.Ser1276Thr)
n.3533T>A
c.4078T>A (p.Ser1360Thr)
c.3979T>A (p.Ser1327Thr)
c.4393T>A (p.Ser1465Thr)
dbSNP
16g.9763308A=CA2206692655GRIN2Ac.4236T= (p.Cys1412=)
c.*47T= (n.*47T=)
n.3486T=
c.3765T= (p.Cys1255=)
c.*1606T= (n.*1606T=)
c.3825T= (p.Cys1275=)
n.3532T=
c.4077T= (p.Cys1359=)
c.3978T= (p.Cys1326=)
c.4392T= (p.Cys1464=)
16g.9763308A>CCA394705636GRIN2Ac.4236T>G (p.Cys1412Trp)
c.*47T>G (n.*47T>G)
n.3486T>G
c.3765T>G (p.Cys1255Trp)
c.*1606T>G (n.*1606T>G)
c.3825T>G (p.Cys1275Trp)
n.3532T>G
c.4077T>G (p.Cys1359Trp)
c.3978T>G (p.Cys1326Trp)
c.4392T>G (p.Cys1464Trp)
16g.9763308A>GCA493692571GRIN2Ac.4236T>C (p.Cys1412=)
c.*47T>C (n.*47T>C)
n.3486T>C
c.3765T>C (p.Cys1255=)
c.*1606T>C (n.*1606T>C)
c.3825T>C (p.Cys1275=)
n.3532T>C
c.4077T>C (p.Cys1359=)
c.3978T>C (p.Cys1326=)
c.4392T>C (p.Cys1464=)
gnomAD v4
16g.9763308A>TCA394705638GRIN2Ac.4236T>A (p.Cys1412Ter)
c.*47T>A (n.*47T>A)
n.3486T>A
c.3765T>A (p.Cys1255Ter)
c.*1606T>A (n.*1606T>A)
c.3825T>A (p.Cys1275Ter)
n.3532T>A
c.4077T>A (p.Cys1359Ter)
c.3978T>A (p.Cys1326Ter)
c.4392T>A (p.Cys1464Ter)
dbSNP
16g.9763309C>ACA394705640GRIN2Ac.4235G>T (p.Cys1412Phe)
c.*46G>T (n.*46G>T)
n.3485G>T
c.3764G>T (p.Cys1255Phe)
c.*1605G>T (n.*1605G>T)
c.3824G>T (p.Cys1275Phe)
n.3531G>T
c.4076G>T (p.Cys1359Phe)
c.3977G>T (p.Cys1326Phe)
c.4391G>T (p.Cys1464Phe)
dbSNP
16g.9763309C=CA2206692656GRIN2Ac.4235G= (p.Cys1412=)
c.*46G= (n.*46G=)
n.3485G=
c.3764G= (p.Cys1255=)
c.*1605G= (n.*1605G=)
c.3824G= (p.Cys1275=)
n.3531G=
c.4076G= (p.Cys1359=)
c.3977G= (p.Cys1326=)
c.4391G= (p.Cys1464=)
16g.9763309C>GCA394705641GRIN2Ac.4235G>C (p.Cys1412Ser)
c.*46G>C (n.*46G>C)
n.3485G>C
c.3764G>C (p.Cys1255Ser)
c.*1605G>C (n.*1605G>C)
c.3824G>C (p.Cys1275Ser)
n.3531G>C
c.4076G>C (p.Cys1359Ser)
c.3977G>C (p.Cys1326Ser)
c.4391G>C (p.Cys1464Ser)
ClinVar dbSNP gnomAD v4
16g.9763309C>TCA394705643GRIN2Ac.4235G>A (p.Cys1412Tyr)
c.*46G>A (n.*46G>A)
n.3485G>A
c.3764G>A (p.Cys1255Tyr)
c.*1605G>A (n.*1605G>A)
c.3824G>A (p.Cys1275Tyr)
n.3531G>A
c.4076G>A (p.Cys1359Tyr)
c.3977G>A (p.Cys1326Tyr)
c.4391G>A (p.Cys1464Tyr)
dbSNP
16g.9763310A=CA2206692657GRIN2Ac.4234T= (p.Cys1412=)
c.*45T= (n.*45T=)
n.3484T=
c.3763T= (p.Cys1255=)
c.*1604T= (n.*1604T=)
c.3823T= (p.Cys1275=)
n.3530T=
c.4075T= (p.Cys1359=)
c.3976T= (p.Cys1326=)
c.4390T= (p.Cys1464=)
16g.9763310A>CCA394705645GRIN2Ac.4234T>G (p.Cys1412Gly)
c.*45T>G (n.*45T>G)
n.3484T>G
c.3763T>G (p.Cys1255Gly)
c.*1604T>G (n.*1604T>G)
c.3823T>G (p.Cys1275Gly)
n.3530T>G
c.4075T>G (p.Cys1359Gly)
c.3976T>G (p.Cys1326Gly)
c.4390T>G (p.Cys1464Gly)
16g.9763310A>GCA394705646GRIN2Ac.4234T>C (p.Cys1412Arg)
c.*45T>C (n.*45T>C)
n.3484T>C
c.3763T>C (p.Cys1255Arg)
c.*1604T>C (n.*1604T>C)
c.3823T>C (p.Cys1275Arg)
n.3530T>C
c.4075T>C (p.Cys1359Arg)
c.3976T>C (p.Cys1326Arg)
c.4390T>C (p.Cys1464Arg)
ClinVar dbSNP gnomAD v2
16g.9763310A>TCA394705648GRIN2Ac.4234T>A (p.Cys1412Ser)
c.*45T>A (n.*45T>A)
n.3484T>A
c.3763T>A (p.Cys1255Ser)
c.*1604T>A (n.*1604T>A)
c.3823T>A (p.Cys1275Ser)
n.3530T>A
c.4075T>A (p.Cys1359Ser)
c.3976T>A (p.Cys1326Ser)
c.4390T>A (p.Cys1464Ser)
ClinVar dbSNP
16g.9763311G>ACA493692574GRIN2Ac.4233C>T (p.Tyr1411=)
c.*44C>T (n.*44C>T)
n.3483C>T
c.3762C>T (p.Tyr1254=)
c.*1603C>T (n.*1603C>T)
c.3822C>T (p.Tyr1274=)
n.3529C>T
c.4074C>T (p.Tyr1358=)
c.3975C>T (p.Tyr1325=)
c.4389C>T (p.Tyr1463=)
dbSNP gnomAD v4
16g.9763311G>CCA394705651GRIN2Ac.4233C>G (p.Tyr1411Ter)
c.*44C>G (n.*44C>G)
n.3483C>G
c.3762C>G (p.Tyr1254Ter)
c.*1603C>G (n.*1603C>G)
c.3822C>G (p.Tyr1274Ter)
n.3529C>G
c.4074C>G (p.Tyr1358Ter)
c.3975C>G (p.Tyr1325Ter)
c.4389C>G (p.Tyr1463Ter)
dbSNP
16g.9763311G>TCA394705652GRIN2Ac.4233C>A (p.Tyr1411Ter)
c.*44C>A (n.*44C>A)
n.3483C>A
c.3762C>A (p.Tyr1254Ter)
c.*1603C>A (n.*1603C>A)
c.3822C>A (p.Tyr1274Ter)
n.3529C>A
c.4074C>A (p.Tyr1358Ter)
c.3975C>A (p.Tyr1325Ter)
c.4389C>A (p.Tyr1463Ter)
16g.9763312T>ACA394705656GRIN2Ac.4232A>T (p.Tyr1411Phe)
c.*43A>T (n.*43A>T)
n.3482A>T
c.3761A>T (p.Tyr1254Phe)
c.*1602A>T (n.*1602A>T)
c.3821A>T (p.Tyr1274Phe)
n.3528A>T
c.4073A>T (p.Tyr1358Phe)
c.3974A>T (p.Tyr1325Phe)
c.4388A>T (p.Tyr1463Phe)
dbSNP
16g.9763312T>CCA394705657GRIN2Ac.4232A>G (p.Tyr1411Cys)
c.*43A>G (n.*43A>G)
n.3482A>G
c.3761A>G (p.Tyr1254Cys)
c.*1602A>G (n.*1602A>G)
c.3821A>G (p.Tyr1274Cys)
n.3528A>G
c.4073A>G (p.Tyr1358Cys)
c.3974A>G (p.Tyr1325Cys)
c.4388A>G (p.Tyr1463Cys)
dbSNP COSMIC
16g.9763312T>GCA394705659GRIN2Ac.4232A>C (p.Tyr1411Ser)
c.*43A>C (n.*43A>C)
n.3482A>C
c.3761A>C (p.Tyr1254Ser)
c.*1602A>C (n.*1602A>C)
c.3821A>C (p.Tyr1274Ser)
n.3528A>C
c.4073A>C (p.Tyr1358Ser)
c.3974A>C (p.Tyr1325Ser)
c.4388A>C (p.Tyr1463Ser)
dbSNP
16g.9763313A>CCA394705661GRIN2Ac.4231T>G (p.Tyr1411Asp)
c.*42T>G (n.*42T>G)
n.3481T>G
c.3760T>G (p.Tyr1254Asp)
c.*1601T>G (n.*1601T>G)
c.3820T>G (p.Tyr1274Asp)
n.3527T>G
c.4072T>G (p.Tyr1358Asp)
c.3973T>G (p.Tyr1325Asp)
c.4387T>G (p.Tyr1463Asp)
COSMIC
16g.9763313A>GCA394705662GRIN2Ac.4231T>C (p.Tyr1411His)
c.*42T>C (n.*42T>C)
n.3481T>C
c.3760T>C (p.Tyr1254His)
c.*1601T>C (n.*1601T>C)
c.3820T>C (p.Tyr1274His)
n.3527T>C
c.4072T>C (p.Tyr1358His)
c.3973T>C (p.Tyr1325His)
c.4387T>C (p.Tyr1463His)
dbSNP
16g.9763313A>TCA394705664GRIN2Ac.4231T>A (p.Tyr1411Asn)
c.*42T>A (n.*42T>A)
n.3481T>A
c.3760T>A (p.Tyr1254Asn)
c.*1601T>A (n.*1601T>A)
c.3820T>A (p.Tyr1274Asn)
n.3527T>A
c.4072T>A (p.Tyr1358Asn)
c.3973T>A (p.Tyr1325Asn)
c.4387T>A (p.Tyr1463Asn)
dbSNP
16g.9763314C>ACA493692577GRIN2Ac.4230G>T (p.Ser1410=)
c.*41G>T (n.*41G>T)
n.3480G>T
c.3759G>T (p.Ser1253=)
c.*1600G>T (n.*1600G>T)
c.3819G>T (p.Ser1273=)
n.3526G>T
c.4071G>T (p.Ser1357=)
c.3972G>T (p.Ser1324=)
c.4386G>T (p.Ser1462=)
dbSNP
16g.9763314C=CA2206692658GRIN2Ac.4230G= (p.Ser1410=)
c.*41G= (n.*41G=)
n.3480G=
c.3759G= (p.Ser1253=)
c.*1600G= (n.*1600G=)
c.3819G= (p.Ser1273=)
n.3526G=
c.4071G= (p.Ser1357=)
c.3972G= (p.Ser1324=)
c.4386G= (p.Ser1462=)
16g.9763314C>GCA493692578GRIN2Ac.4230G>C (p.Ser1410=)
c.*41G>C (n.*41G>C)
n.3480G>C
c.3759G>C (p.Ser1253=)
c.*1600G>C (n.*1600G>C)
c.3819G>C (p.Ser1273=)
n.3526G>C
c.4071G>C (p.Ser1357=)
c.3972G>C (p.Ser1324=)
c.4386G>C (p.Ser1462=)
dbSNP gnomAD v4
16g.9763314C>TCA7896191GRIN2Ac.4230G>A (p.Ser1410=)
c.*41G>A (n.*41G>A)
n.3480G>A
c.3759G>A (p.Ser1253=)
c.*1600G>A (n.*1600G>A)
c.3819G>A (p.Ser1273=)
n.3526G>A
c.4071G>A (p.Ser1357=)
c.3972G>A (p.Ser1324=)
c.4386G>A (p.Ser1462=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.9763315G>ACA394705667GRIN2Ac.4229C>T (p.Ser1410Leu)
c.*40C>T (n.*40C>T)
n.3479C>T
c.3758C>T (p.Ser1253Leu)
c.*1599C>T (n.*1599C>T)
c.3818C>T (p.Ser1273Leu)
n.3525C>T
c.4070C>T (p.Ser1357Leu)
c.3971C>T (p.Ser1324Leu)
c.4385C>T (p.Ser1462Leu)
ClinVar dbSNP gnomAD v4 COSMIC
16g.9763315G>CCA394705670GRIN2Ac.4229C>G (p.Ser1410Trp)
c.*40C>G (n.*40C>G)
n.3479C>G
c.3758C>G (p.Ser1253Trp)
c.*1599C>G (n.*1599C>G)
c.3818C>G (p.Ser1273Trp)
n.3525C>G
c.4070C>G (p.Ser1357Trp)
c.3971C>G (p.Ser1324Trp)
c.4385C>G (p.Ser1462Trp)
dbSNP gnomAD v4
16g.9763315G=CA2206692659GRIN2Ac.4229C= (p.Ser1410=)
c.*40C= (n.*40C=)
n.3479C=
c.3758C= (p.Ser1253=)
c.*1599C= (n.*1599C=)
c.3818C= (p.Ser1273=)
n.3525C=
c.4070C= (p.Ser1357=)
c.3971C= (p.Ser1324=)
c.4385C= (p.Ser1462=)
16g.9763315G>TCA394705671GRIN2Ac.4229C>A (p.Ser1410Ter)
c.*40C>A (n.*40C>A)
n.3479C>A
c.3758C>A (p.Ser1253Ter)
c.*1599C>A (n.*1599C>A)
c.3818C>A (p.Ser1273Ter)
n.3525C>A
c.4070C>A (p.Ser1357Ter)
c.3971C>A (p.Ser1324Ter)
c.4385C>A (p.Ser1462Ter)
dbSNP
16g.9763316A>CCA394705673GRIN2Ac.4228T>G (p.Ser1410Ala)
c.*39T>G (n.*39T>G)
n.3478T>G
c.3757T>G (p.Ser1253Ala)
c.*1598T>G (n.*1598T>G)
c.3817T>G (p.Ser1273Ala)
n.3524T>G
c.4069T>G (p.Ser1357Ala)
c.3970T>G (p.Ser1324Ala)
c.4384T>G (p.Ser1462Ala)
16g.9763316A>GCA394705675GRIN2Ac.4228T>C (p.Ser1410Pro)
c.*39T>C (n.*39T>C)
n.3478T>C
c.3757T>C (p.Ser1253Pro)
c.*1598T>C (n.*1598T>C)
c.3817T>C (p.Ser1273Pro)
n.3524T>C
c.4069T>C (p.Ser1357Pro)
c.3970T>C (p.Ser1324Pro)
c.4384T>C (p.Ser1462Pro)
16g.9763316A>TCA394705676GRIN2Ac.4228T>A (p.Ser1410Thr)
c.*39T>A (n.*39T>A)
n.3478T>A
c.3757T>A (p.Ser1253Thr)
c.*1598T>A (n.*1598T>A)
c.3817T>A (p.Ser1273Thr)
n.3524T>A
c.4069T>A (p.Ser1357Thr)
c.3970T>A (p.Ser1324Thr)
c.4384T>A (p.Ser1462Thr)
16g.9763317T>ACA493692584GRIN2Ac.4227A>T (p.Ala1409=)
c.*38A>T (n.*38A>T)
n.3477A>T
c.3756A>T (p.Ala1252=)
c.*1597A>T (n.*1597A>T)
c.3816A>T (p.Ala1272=)
n.3523A>T
c.4068A>T (p.Ala1356=)
c.3969A>T (p.Ala1323=)
c.4383A>T (p.Ala1461=)
dbSNP
16g.9763317T>CCA7896192GRIN2Ac.4227A>G (p.Ala1409=)
c.*38A>G (n.*38A>G)
n.3477A>G
c.3756A>G (p.Ala1252=)
c.*1597A>G (n.*1597A>G)
c.3816A>G (p.Ala1272=)
n.3523A>G
c.4068A>G (p.Ala1356=)
c.3969A>G (p.Ala1323=)
c.4383A>G (p.Ala1461=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
16g.9763317T>GCA493692583GRIN2Ac.4227A>C (p.Ala1409=)
c.*38A>C (n.*38A>C)
n.3477A>C
c.3756A>C (p.Ala1252=)
c.*1597A>C (n.*1597A>C)
c.3816A>C (p.Ala1272=)
n.3523A>C
c.4068A>C (p.Ala1356=)
c.3969A>C (p.Ala1323=)
c.4383A>C (p.Ala1461=)
COSMIC
16g.9763317T=CA2206692660GRIN2Ac.4227A= (p.Ala1409=)
c.*38A= (n.*38A=)
n.3477A=
c.3756A= (p.Ala1252=)
c.*1597A= (n.*1597A=)
c.3816A= (p.Ala1272=)
n.3523A=
c.4068A= (p.Ala1356=)
c.3969A= (p.Ala1323=)
c.4383A= (p.Ala1461=)
16g.9763318G>ACA394705680GRIN2Ac.4226C>T (p.Ala1409Val)
c.*37C>T (n.*37C>T)
n.3476C>T
c.3755C>T (p.Ala1252Val)
c.*1596C>T (n.*1596C>T)
c.3815C>T (p.Ala1272Val)
n.3522C>T
c.4067C>T (p.Ala1356Val)
c.3968C>T (p.Ala1323Val)
c.4382C>T (p.Ala1461Val)
dbSNP gnomAD v4 COSMIC
16g.9763318G>CCA394705682GRIN2Ac.4226C>G (p.Ala1409Gly)
c.*37C>G (n.*37C>G)
n.3476C>G
c.3755C>G (p.Ala1252Gly)
c.*1596C>G (n.*1596C>G)
c.3815C>G (p.Ala1272Gly)
n.3522C>G
c.4067C>G (p.Ala1356Gly)
c.3968C>G (p.Ala1323Gly)
c.4382C>G (p.Ala1461Gly)
dbSNP
16g.9763318G>TCA394705684GRIN2Ac.4226C>A (p.Ala1409Glu)
c.*37C>A (n.*37C>A)
n.3476C>A
c.3755C>A (p.Ala1252Glu)
c.*1596C>A (n.*1596C>A)
c.3815C>A (p.Ala1272Glu)
n.3522C>A
c.4067C>A (p.Ala1356Glu)
c.3968C>A (p.Ala1323Glu)
c.4382C>A (p.Ala1461Glu)
dbSNP
16g.9763319C>ACA394705686GRIN2Ac.4225G>T (p.Ala1409Ser)
c.*36G>T (n.*36G>T)
n.3475G>T
c.3754G>T (p.Ala1252Ser)
c.*1595G>T (n.*1595G>T)
c.3814G>T (p.Ala1272Ser)
n.3521G>T
c.4066G>T (p.Ala1356Ser)
c.3967G>T (p.Ala1323Ser)
c.4381G>T (p.Ala1461Ser)
dbSNP
16g.9763319C=CA2206692661GRIN2Ac.4225G= (p.Ala1409=)
c.*36G= (n.*36G=)
n.3475G=
c.3754G= (p.Ala1252=)
c.*1595G= (n.*1595G=)
c.3814G= (p.Ala1272=)
n.3521G=
c.4066G= (p.Ala1356=)
c.3967G= (p.Ala1323=)
c.4381G= (p.Ala1461=)
16g.9763319C>GCA394705688GRIN2Ac.4225G>C (p.Ala1409Pro)
c.*36G>C (n.*36G>C)
n.3475G>C
c.3754G>C (p.Ala1252Pro)
c.*1595G>C (n.*1595G>C)
c.3814G>C (p.Ala1272Pro)
n.3521G>C
c.4066G>C (p.Ala1356Pro)
c.3967G>C (p.Ala1323Pro)
c.4381G>C (p.Ala1461Pro)
dbSNP gnomAD v4
16g.9763319C>TCA394705690GRIN2Ac.4225G>A (p.Ala1409Thr)
c.*36G>A (n.*36G>A)
n.3475G>A
c.3754G>A (p.Ala1252Thr)
c.*1595G>A (n.*1595G>A)
c.3814G>A (p.Ala1272Thr)
n.3521G>A
c.4066G>A (p.Ala1356Thr)
c.3967G>A (p.Ala1323Thr)
c.4381G>A (p.Ala1461Thr)
dbSNP
16g.9763320C>ACA493692585GRIN2Ac.4224G>T (p.Thr1408=)
c.*35G>T (n.*35G>T)
n.3474G>T
c.3753G>T (p.Thr1251=)
c.*1594G>T (n.*1594G>T)
c.3813G>T (p.Thr1271=)
n.3520G>T
c.4065G>T (p.Thr1355=)
c.3966G>T (p.Thr1322=)
c.4380G>T (p.Thr1460=)
dbSNP gnomAD v4
16g.9763320C=CA2206692662GRIN2Ac.4224G= (p.Thr1408=)
c.*35G= (n.*35G=)
n.3474G=
c.3753G= (p.Thr1251=)
c.*1594G= (n.*1594G=)
c.3813G= (p.Thr1271=)
n.3520G=
c.4065G= (p.Thr1355=)
c.3966G= (p.Thr1322=)
c.4380G= (p.Thr1460=)
16g.9763320C>GCA493692586GRIN2Ac.4224G>C (p.Thr1408=)
c.*35G>C (n.*35G>C)
n.3474G>C
c.3753G>C (p.Thr1251=)
c.*1594G>C (n.*1594G>C)
c.3813G>C (p.Thr1271=)
n.3520G>C
c.4065G>C (p.Thr1355=)
c.3966G>C (p.Thr1322=)
c.4380G>C (p.Thr1460=)
16g.9763320C>TCA7896193GRIN2Ac.4224G>A (p.Thr1408=)
c.*35G>A (n.*35G>A)
n.3474G>A
c.3753G>A (p.Thr1251=)
c.*1594G>A (n.*1594G>A)
c.3813G>A (p.Thr1271=)
n.3520G>A
c.4065G>A (p.Thr1355=)
c.3966G>A (p.Thr1322=)
c.4380G>A (p.Thr1460=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.9763321G>ACA7896194GRIN2Ac.4223C>T (p.Thr1408Met)
c.*34C>T (n.*34C>T)
n.3473C>T
c.3752C>T (p.Thr1251Met)
c.*1593C>T (n.*1593C>T)
c.3812C>T (p.Thr1271Met)
n.3519C>T
c.4064C>T (p.Thr1355Met)
c.3965C>T (p.Thr1322Met)
c.4379C>T (p.Thr1460Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.9763321G>CCA394705694GRIN2Ac.4223C>G (p.Thr1408Arg)
c.*34C>G (n.*34C>G)
n.3473C>G
c.3752C>G (p.Thr1251Arg)
c.*1593C>G (n.*1593C>G)
c.3812C>G (p.Thr1271Arg)
n.3519C>G
c.4064C>G (p.Thr1355Arg)
c.3965C>G (p.Thr1322Arg)
c.4379C>G (p.Thr1460Arg)
dbSNP gnomAD v4
16g.9763321G=CA2206692663GRIN2Ac.4223C= (p.Thr1408=)
c.*34C= (n.*34C=)
n.3473C=
c.3752C= (p.Thr1251=)
c.*1593C= (n.*1593C=)
c.3812C= (p.Thr1271=)
n.3519C=
c.4064C= (p.Thr1355=)
c.3965C= (p.Thr1322=)
c.4379C= (p.Thr1460=)
16g.9763321G>TCA394705696GRIN2Ac.4223C>A (p.Thr1408Lys)
c.*34C>A (n.*34C>A)
n.3473C>A
c.3752C>A (p.Thr1251Lys)
c.*1593C>A (n.*1593C>A)
c.3812C>A (p.Thr1271Lys)
n.3519C>A
c.4064C>A (p.Thr1355Lys)
c.3965C>A (p.Thr1322Lys)
c.4379C>A (p.Thr1460Lys)
dbSNP gnomAD v2 gnomAD v4
16g.9763322T>ACA394705697GRIN2Ac.4222A>T (p.Thr1408Ser)
c.*33A>T (n.*33A>T)
n.3472A>T
c.3751A>T (p.Thr1251Ser)
c.*1592A>T (n.*1592A>T)
c.3811A>T (p.Thr1271Ser)
n.3518A>T
c.4063A>T (p.Thr1355Ser)
c.3964A>T (p.Thr1322Ser)
c.4378A>T (p.Thr1460Ser)
dbSNP
16g.9763322T>CCA394705699GRIN2Ac.4222A>G (p.Thr1408Ala)
c.*33A>G (n.*33A>G)
n.3472A>G
c.3751A>G (p.Thr1251Ala)
c.*1592A>G (n.*1592A>G)
c.3811A>G (p.Thr1271Ala)
n.3518A>G
c.4063A>G (p.Thr1355Ala)
c.3964A>G (p.Thr1322Ala)
c.4378A>G (p.Thr1460Ala)
dbSNP COSMIC
16g.9763322T>GCA394705701GRIN2Ac.4222A>C (p.Thr1408Pro)
c.*33A>C (n.*33A>C)
n.3472A>C
c.3751A>C (p.Thr1251Pro)
c.*1592A>C (n.*1592A>C)
c.3811A>C (p.Thr1271Pro)
n.3518A>C
c.4063A>C (p.Thr1355Pro)
c.3964A>C (p.Thr1322Pro)
c.4378A>C (p.Thr1460Pro)
dbSNP
16g.9763323T>ACA493692592GRIN2Ac.4221A>T (p.Ser1407=)
c.*32A>T (n.*32A>T)
n.3471A>T
c.3750A>T (p.Ser1250=)
c.*1591A>T (n.*1591A>T)
c.3810A>T (p.Ser1270=)
n.3517A>T
c.4062A>T (p.Ser1354=)
c.3963A>T (p.Ser1321=)
c.4377A>T (p.Ser1459=)
dbSNP
16g.9763323T>CCA493692590GRIN2Ac.4221A>G (p.Ser1407=)
c.*32A>G (n.*32A>G)
n.3471A>G
c.3750A>G (p.Ser1250=)
c.*1591A>G (n.*1591A>G)
c.3810A>G (p.Ser1270=)
n.3517A>G
c.4062A>G (p.Ser1354=)
c.3963A>G (p.Ser1321=)
c.4377A>G (p.Ser1459=)
dbSNP
16g.9763323T>GCA493692591GRIN2Ac.4221A>C (p.Ser1407=)
c.*32A>C (n.*32A>C)
n.3471A>C
c.3750A>C (p.Ser1250=)
c.*1591A>C (n.*1591A>C)
c.3810A>C (p.Ser1270=)
n.3517A>C
c.4062A>C (p.Ser1354=)
c.3963A>C (p.Ser1321=)
c.4377A>C (p.Ser1459=)
dbSNP
16g.9763324G>ACA7896195GRIN2Ac.4220C>T (p.Ser1407Leu)
c.*31C>T (n.*31C>T)
n.3470C>T
c.3749C>T (p.Ser1250Leu)
c.*1590C>T (n.*1590C>T)
c.3809C>T (p.Ser1270Leu)
n.3516C>T
c.4061C>T (p.Ser1354Leu)
c.3962C>T (p.Ser1321Leu)
c.4376C>T (p.Ser1459Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
16g.9763324G>CCA394705706GRIN2Ac.4220C>G (p.Ser1407Ter)
c.*31C>G (n.*31C>G)
n.3470C>G
c.3749C>G (p.Ser1250Ter)
c.*1590C>G (n.*1590C>G)
c.3809C>G (p.Ser1270Ter)
n.3516C>G
c.4061C>G (p.Ser1354Ter)
c.3962C>G (p.Ser1321Ter)
c.4376C>G (p.Ser1459Ter)
dbSNP
16g.9763324G=CA2206692664GRIN2Ac.4220C= (p.Ser1407=)
c.*31C= (n.*31C=)
n.3470C=
c.3749C= (p.Ser1250=)
c.*1590C= (n.*1590C=)
c.3809C= (p.Ser1270=)
n.3516C=
c.4061C= (p.Ser1354=)
c.3962C= (p.Ser1321=)
c.4376C= (p.Ser1459=)
16g.9763324G>TCA394705703GRIN2Ac.4220C>A (p.Ser1407Ter)
c.*31C>A (n.*31C>A)
n.3470C>A
c.3749C>A (p.Ser1250Ter)
c.*1590C>A (n.*1590C>A)
c.3809C>A (p.Ser1270Ter)
n.3516C>A
c.4061C>A (p.Ser1354Ter)
c.3962C>A (p.Ser1321Ter)
c.4376C>A (p.Ser1459Ter)
dbSNP
16g.9763325A>CCA394705709GRIN2Ac.4219T>G (p.Ser1407Ala)
c.*30T>G (n.*30T>G)
n.3469T>G
c.3748T>G (p.Ser1250Ala)
c.*1589T>G (n.*1589T>G)
c.3808T>G (p.Ser1270Ala)
n.3515T>G
c.4060T>G (p.Ser1354Ala)
c.3961T>G (p.Ser1321Ala)
c.4375T>G (p.Ser1459Ala)
ClinVar
16g.9763325A>GCA394705711GRIN2Ac.4219T>C (p.Ser1407Pro)
c.*30T>C (n.*30T>C)
n.3469T>C
c.3748T>C (p.Ser1250Pro)
c.*1589T>C (n.*1589T>C)
c.3808T>C (p.Ser1270Pro)
n.3515T>C
c.4060T>C (p.Ser1354Pro)
c.3961T>C (p.Ser1321Pro)
c.4375T>C (p.Ser1459Pro)
dbSNP
16g.9763325A>TCA394705714GRIN2Ac.4219T>A (p.Ser1407Thr)
c.*30T>A (n.*30T>A)
n.3469T>A
c.3748T>A (p.Ser1250Thr)
c.*1589T>A (n.*1589T>A)
c.3808T>A (p.Ser1270Thr)
n.3515T>A
c.4060T>A (p.Ser1354Thr)
c.3961T>A (p.Ser1321Thr)
c.4375T>A (p.Ser1459Thr)
dbSNP gnomAD v4
16g.9763326C>ACA394705716GRIN2Ac.4218G>T (p.Arg1406Ser)
c.*29G>T (n.*29G>T)
n.3468G>T
c.3747G>T (p.Arg1249Ser)
c.*1588G>T (n.*1588G>T)
c.3807G>T (p.Arg1269Ser)
n.3514G>T
c.4059G>T (p.Arg1353Ser)
c.3960G>T (p.Arg1320Ser)
c.4374G>T (p.Arg1458Ser)
dbSNP
16g.9763326C=CA2206692665GRIN2Ac.4218G= (p.Arg1406=)
c.*29G= (n.*29G=)
n.3468G=
c.3747G= (p.Arg1249=)
c.*1588G= (n.*1588G=)
c.3807G= (p.Arg1269=)
n.3514G=
c.4059G= (p.Arg1353=)
c.3960G= (p.Arg1320=)
c.4374G= (p.Arg1458=)
16g.9763326C>GCA394705718GRIN2Ac.4218G>C (p.Arg1406Ser)
c.*29G>C (n.*29G>C)
n.3468G>C
c.3747G>C (p.Arg1249Ser)
c.*1588G>C (n.*1588G>C)
c.3807G>C (p.Arg1269Ser)
n.3514G>C
c.4059G>C (p.Arg1353Ser)
c.3960G>C (p.Arg1320Ser)
c.4374G>C (p.Arg1458Ser)
dbSNP
16g.9763326C>TCA7896196GRIN2Ac.4218G>A (p.Arg1406=)
c.*29G>A (n.*29G>A)
n.3468G>A
c.3747G>A (p.Arg1249=)
c.*1588G>A (n.*1588G>A)
c.3807G>A (p.Arg1269=)
n.3514G>A
c.4059G>A (p.Arg1353=)
c.3960G>A (p.Arg1320=)
c.4374G>A (p.Arg1458=)
dbSNP ExAC gnomAD v2 gnomAD v4
16g.9763326_9763327insAAACCTAGGGAGCTAGACCTTAGCAGGCCCTCCCGGAGCATAAGCCA2805819919GRIN2Ac.4218_4219insCTTATGCTCCGGGAGGGCCTGCTAAGGTCTAGCTCCCTAGGTTTG (p.Arg1406_Ser1407insLeuMetLeuArgGluGlyLeuLeuArgSerSerSerLeuGlyLeu)
c.*29_*30insCTTATGCTCCGGGAGGGCCTGCTAAGGTCTAGCTCCCTAGGTTTG (n.*29_*30insCTTATGCTCCGGGAGGGCCTGCTAAGGTCTAGCTCCCTAGGTTTG)
n.3468_3469insCTTATGCTCCGGGAGGGCCTGCTAAGGTCTAGCTCCCTAGGTTTG
c.3747_3748insCTTATGCTCCGGGAGGGCCTGCTAAGGTCTAGCTCCCTAGGTTTG (p.Arg1249_Ser1250insLeuMetLeuArgGluGlyLeuLeuArgSerSerSerLeuGlyLeu)
c.*1588_*1589insCTTATGCTCCGGGAGGGCCTGCTAAGGTCTAGCTCCCTAGGTTTG (n.*1588_*1589insCTTATGCTCCGGGAGGGCCTGCTAAGGTCTAGCTCCCTAGGTTTG)
c.3807_3808insCTTATGCTCCGGGAGGGCCTGCTAAGGTCTAGCTCCCTAGGTTTG (p.Arg1269_Ser1270insLeuMetLeuArgGluGlyLeuLeuArgSerSerSerLeuGlyLeu)
n.3514_3515insCTTATGCTCCGGGAGGGCCTGCTAAGGTCTAGCTCCCTAGGTTTG
c.4059_4060insCTTATGCTCCGGGAGGGCCTGCTAAGGTCTAGCTCCCTAGGTTTG (p.Arg1353_Ser1354insLeuMetLeuArgGluGlyLeuLeuArgSerSerSerLeuGlyLeu)
c.3960_3961insCTTATGCTCCGGGAGGGCCTGCTAAGGTCTAGCTCCCTAGGTTTG (p.Arg1320_Ser1321insLeuMetLeuArgGluGlyLeuLeuArgSerSerSerLeuGlyLeu)
c.4374_4375insCTTATGCTCCGGGAGGGCCTGCTAAGGTCTAGCTCCCTAGGTTTG (p.Arg1458_Ser1459insLeuMetLeuArgGluGlyLeuLeuArgSerSerSerLeuGlyLeu)
16g.9763327C>ACA394705722GRIN2Ac.4217G>T (p.Arg1406Met)
c.*28G>T (n.*28G>T)
n.3467G>T
c.3746G>T (p.Arg1249Met)
c.*1587G>T (n.*1587G>T)
c.3806G>T (p.Arg1269Met)
n.3513G>T
c.4058G>T (p.Arg1353Met)
c.3959G>T (p.Arg1320Met)
c.4373G>T (p.Arg1458Met)
dbSNP
16g.9763327C=CA2206692666GRIN2Ac.4217G= (p.Arg1406=)
c.*28G= (n.*28G=)
n.3467G=
c.3746G= (p.Arg1249=)
c.*1587G= (n.*1587G=)
c.3806G= (p.Arg1269=)
n.3513G=
c.4058G= (p.Arg1353=)
c.3959G= (p.Arg1320=)
c.4373G= (p.Arg1458=)
16g.9763327C>GCA394705726GRIN2Ac.4217G>C (p.Arg1406Thr)
c.*28G>C (n.*28G>C)
n.3467G>C
c.3746G>C (p.Arg1249Thr)
c.*1587G>C (n.*1587G>C)
c.3806G>C (p.Arg1269Thr)
n.3513G>C
c.4058G>C (p.Arg1353Thr)
c.3959G>C (p.Arg1320Thr)
c.4373G>C (p.Arg1458Thr)
16g.9763327C>TCA394705724GRIN2Ac.4217G>A (p.Arg1406Lys)
c.*28G>A (n.*28G>A)
n.3467G>A
c.3746G>A (p.Arg1249Lys)
c.*1587G>A (n.*1587G>A)
c.3806G>A (p.Arg1269Lys)
n.3513G>A
c.4058G>A (p.Arg1353Lys)
c.3959G>A (p.Arg1320Lys)
c.4373G>A (p.Arg1458Lys)
dbSNP gnomAD v3 gnomAD v4
16g.9763328T>ACA394705728GRIN2Ac.4216A>T (p.Arg1406Trp)
c.*27A>T (n.*27A>T)
n.3466A>T
c.3745A>T (p.Arg1249Trp)
c.*1586A>T (n.*1586A>T)
c.3805A>T (p.Arg1269Trp)
n.3512A>T
c.4057A>T (p.Arg1353Trp)
c.3958A>T (p.Arg1320Trp)
c.4372A>T (p.Arg1458Trp)
dbSNP
16g.9763328T>CCA394705730GRIN2Ac.4216A>G (p.Arg1406Gly)
c.*27A>G (n.*27A>G)
n.3466A>G
c.3745A>G (p.Arg1249Gly)
c.*1586A>G (n.*1586A>G)
c.3805A>G (p.Arg1269Gly)
n.3512A>G
c.4057A>G (p.Arg1353Gly)
c.3958A>G (p.Arg1320Gly)
c.4372A>G (p.Arg1458Gly)
dbSNP
16g.9763328T>GCA493692465GRIN2Ac.4216A>C (p.Arg1406=)
c.*27A>C (n.*27A>C)
n.3466A>C
c.3745A>C (p.Arg1249=)
c.*1586A>C (n.*1586A>C)
c.3805A>C (p.Arg1269=)
n.3512A>C
c.4057A>C (p.Arg1353=)
c.3958A>C (p.Arg1320=)
c.4372A>C (p.Arg1458=)
16g.9763329C>ACA394705733GRIN2Ac.4215G>T (p.Leu1405Phe)
c.*26G>T (n.*26G>T)
n.3465G>T
c.3744G>T (p.Leu1248Phe)
c.*1585G>T (n.*1585G>T)
c.3804G>T (p.Leu1268Phe)
n.3511G>T
c.4056G>T (p.Leu1352Phe)
c.3957G>T (p.Leu1319Phe)
c.4371G>T (p.Leu1457Phe)
dbSNP gnomAD v2 gnomAD v4
16g.9763329C=CA2206692667GRIN2Ac.4215G= (p.Leu1405=)
c.*26G= (n.*26G=)
n.3465G=
c.3744G= (p.Leu1248=)
c.*1585G= (n.*1585G=)
c.3804G= (p.Leu1268=)
n.3511G=
c.4056G= (p.Leu1352=)
c.3957G= (p.Leu1319=)
c.4371G= (p.Leu1457=)
16g.9763329C>GCA394705735GRIN2Ac.4215G>C (p.Leu1405Phe)
c.*26G>C (n.*26G>C)
n.3465G>C
c.3744G>C (p.Leu1248Phe)
c.*1585G>C (n.*1585G>C)
c.3804G>C (p.Leu1268Phe)
n.3511G>C
c.4056G>C (p.Leu1352Phe)
c.3957G>C (p.Leu1319Phe)
c.4371G>C (p.Leu1457Phe)
dbSNP gnomAD v4
16g.9763329C>TCA493692466GRIN2Ac.4215G>A (p.Leu1405=)
c.*26G>A (n.*26G>A)
n.3465G>A
c.3744G>A (p.Leu1248=)
c.*1585G>A (n.*1585G>A)
c.3804G>A (p.Leu1268=)
n.3511G>A
c.4056G>A (p.Leu1352=)
c.3957G>A (p.Leu1319=)
c.4371G>A (p.Leu1457=)
dbSNP COSMIC
16g.9763330A=CA2206692668GRIN2Ac.4214T= (p.Leu1405=)
c.*25T= (n.*25T=)
n.3464T=
c.3743T= (p.Leu1248=)
c.*1584T= (n.*1584T=)
c.3803T= (p.Leu1268=)
n.3510T=
c.4055T= (p.Leu1352=)
c.3956T= (p.Leu1319=)
c.4370T= (p.Leu1457=)
16g.9763330A>CCA394705738GRIN2Ac.4214T>G (p.Leu1405Trp)
c.*25T>G (n.*25T>G)
n.3464T>G
c.3743T>G (p.Leu1248Trp)
c.*1584T>G (n.*1584T>G)
c.3803T>G (p.Leu1268Trp)
n.3510T>G
c.4055T>G (p.Leu1352Trp)
c.3956T>G (p.Leu1319Trp)
c.4370T>G (p.Leu1457Trp)
16g.9763330A>GCA394705740GRIN2Ac.4214T>C (p.Leu1405Ser)
c.*25T>C (n.*25T>C)
n.3464T>C
c.3743T>C (p.Leu1248Ser)
c.*1584T>C (n.*1584T>C)
c.3803T>C (p.Leu1268Ser)
n.3510T>C
c.4055T>C (p.Leu1352Ser)
c.3956T>C (p.Leu1319Ser)
c.4370T>C (p.Leu1457Ser)
dbSNP
16g.9763330A>TCA394705741GRIN2Ac.4214T>A (p.Leu1405Ter)
c.*25T>A (n.*25T>A)
n.3464T>A
c.3743T>A (p.Leu1248Ter)
c.*1584T>A (n.*1584T>A)
c.3803T>A (p.Leu1268Ter)
n.3510T>A
c.4055T>A (p.Leu1352Ter)
c.3956T>A (p.Leu1319Ter)
c.4370T>A (p.Leu1457Ter)
dbSNP
16g.9763331A>CCA394705744GRIN2Ac.4213T>G (p.Leu1405Val)
c.*24T>G (n.*24T>G)
n.3463T>G
c.3742T>G (p.Leu1248Val)
c.*1583T>G (n.*1583T>G)
c.3802T>G (p.Leu1268Val)
n.3509T>G
c.4054T>G (p.Leu1352Val)
c.3955T>G (p.Leu1319Val)
c.4369T>G (p.Leu1457Val)
16g.9763331A>GCA493692470GRIN2Ac.4213T>C (p.Leu1405=)
c.*24T>C (n.*24T>C)
n.3463T>C
c.3742T>C (p.Leu1248=)
c.*1583T>C (n.*1583T>C)
c.3802T>C (p.Leu1268=)
n.3509T>C
c.4054T>C (p.Leu1352=)
c.3955T>C (p.Leu1319=)
c.4369T>C (p.Leu1457=)
dbSNP
16g.9763331A>TCA394705745GRIN2Ac.4213T>A (p.Leu1405Met)
c.*24T>A (n.*24T>A)
n.3463T>A
c.3742T>A (p.Leu1248Met)
c.*1583T>A (n.*1583T>A)
c.3802T>A (p.Leu1268Met)
n.3509T>A
c.4054T>A (p.Leu1352Met)
c.3955T>A (p.Leu1319Met)
c.4369T>A (p.Leu1457Met)
dbSNP
16g.9763332G>ACA493692471GRIN2Ac.4212C>T (p.Ser1404=)
c.*23C>T (n.*23C>T)
n.3462C>T
c.3741C>T (p.Ser1247=)
c.*1582C>T (n.*1582C>T)
c.3801C>T (p.Ser1267=)
n.3508C>T
c.4053C>T (p.Ser1351=)
c.3954C>T (p.Ser1318=)
c.4368C>T (p.Ser1456=)
COSMIC
16g.9763332G>CCA493692472GRIN2Ac.4212C>G (p.Ser1404=)
c.*23C>G (n.*23C>G)
n.3462C>G
c.3741C>G (p.Ser1247=)
c.*1582C>G (n.*1582C>G)
c.3801C>G (p.Ser1267=)
n.3508C>G
c.4053C>G (p.Ser1351=)
c.3954C>G (p.Ser1318=)
c.4368C>G (p.Ser1456=)
dbSNP
16g.9763332G=CA2206692669GRIN2Ac.4212C= (p.Ser1404=)
c.*23C= (n.*23C=)
n.3462C=
c.3741C= (p.Ser1247=)
c.*1582C= (n.*1582C=)
c.3801C= (p.Ser1267=)
n.3508C=
c.4053C= (p.Ser1351=)
c.3954C= (p.Ser1318=)
c.4368C= (p.Ser1456=)
16g.9763332G>TCA7896197GRIN2Ac.4212C>A (p.Ser1404=)
c.*23C>A (n.*23C>A)
n.3462C>A
c.3741C>A (p.Ser1247=)
c.*1582C>A (n.*1582C>A)
c.3801C>A (p.Ser1267=)
n.3508C>A
c.4053C>A (p.Ser1351=)
c.3954C>A (p.Ser1318=)
c.4368C>A (p.Ser1456=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.9763333G>ACA277535949GRIN2Ac.4211C>T (p.Ser1404Phe)
c.*22C>T (n.*22C>T)
n.3461C>T
c.3740C>T (p.Ser1247Phe)
c.*1581C>T (n.*1581C>T)
c.3800C>T (p.Ser1267Phe)
n.3507C>T
c.4052C>T (p.Ser1351Phe)
c.3953C>T (p.Ser1318Phe)
c.4367C>T (p.Ser1456Phe)
dbSNP gnomAD v4
16g.9763333G>CCA394705752GRIN2Ac.4211C>G (p.Ser1404Cys)
c.*22C>G (n.*22C>G)
n.3461C>G
c.3740C>G (p.Ser1247Cys)
c.*1581C>G (n.*1581C>G)
c.3800C>G (p.Ser1267Cys)
n.3507C>G
c.4052C>G (p.Ser1351Cys)
c.3953C>G (p.Ser1318Cys)
c.4367C>G (p.Ser1456Cys)
dbSNP gnomAD v4
16g.9763333G=CA2206692670GRIN2Ac.4211C= (p.Ser1404=)
c.*22C= (n.*22C=)
n.3461C=
c.3740C= (p.Ser1247=)
c.*1581C= (n.*1581C=)
c.3800C= (p.Ser1267=)
n.3507C=
c.4052C= (p.Ser1351=)
c.3953C= (p.Ser1318=)
c.4367C= (p.Ser1456=)
16g.9763333G>TCA394705750GRIN2Ac.4211C>A (p.Ser1404Tyr)
c.*22C>A (n.*22C>A)
n.3461C>A
c.3740C>A (p.Ser1247Tyr)
c.*1581C>A (n.*1581C>A)
c.3800C>A (p.Ser1267Tyr)
n.3507C>A
c.4052C>A (p.Ser1351Tyr)
c.3953C>A (p.Ser1318Tyr)
c.4367C>A (p.Ser1456Tyr)
16g.9763334A>CCA394705755GRIN2Ac.4210T>G (p.Ser1404Ala)
c.*21T>G (n.*21T>G)
n.3460T>G
c.3739T>G (p.Ser1247Ala)
c.*1580T>G (n.*1580T>G)
c.3799T>G (p.Ser1267Ala)
n.3506T>G
c.4051T>G (p.Ser1351Ala)
c.3952T>G (p.Ser1318Ala)
c.4366T>G (p.Ser1456Ala)
16g.9763334A>GCA394705759GRIN2Ac.4210T>C (p.Ser1404Pro)
c.*21T>C (n.*21T>C)
n.3460T>C
c.3739T>C (p.Ser1247Pro)
c.*1580T>C (n.*1580T>C)
c.3799T>C (p.Ser1267Pro)
n.3506T>C
c.4051T>C (p.Ser1351Pro)
c.3952T>C (p.Ser1318Pro)
c.4366T>C (p.Ser1456Pro)
dbSNP
16g.9763334A>TCA394705757GRIN2Ac.4210T>A (p.Ser1404Thr)
c.*21T>A (n.*21T>A)
n.3460T>A
c.3739T>A (p.Ser1247Thr)
c.*1580T>A (n.*1580T>A)
c.3799T>A (p.Ser1267Thr)
n.3506T>A
c.4051T>A (p.Ser1351Thr)
c.3952T>A (p.Ser1318Thr)
c.4366T>A (p.Ser1456Thr)
dbSNP
16g.9763335C>ACA493692476GRIN2Ac.4209G>T (p.Ser1403=)
c.*20G>T (n.*20G>T)
n.3459G>T
c.3738G>T (p.Ser1246=)
c.*1579G>T (n.*1579G>T)
c.3798G>T (p.Ser1266=)
n.3505G>T
c.4050G>T (p.Ser1350=)
c.3951G>T (p.Ser1317=)
c.4365G>T (p.Ser1455=)
dbSNP
16g.9763335C=CA2206692671GRIN2Ac.4209G= (p.Ser1403=)
c.*20G= (n.*20G=)
n.3459G=
c.3738G= (p.Ser1246=)
c.*1579G= (n.*1579G=)
c.3798G= (p.Ser1266=)
n.3505G=
c.4050G= (p.Ser1350=)
c.3951G= (p.Ser1317=)
c.4365G= (p.Ser1455=)
16g.9763335C>GCA493692477GRIN2Ac.4209G>C (p.Ser1403=)
c.*20G>C (n.*20G>C)
n.3459G>C
c.3738G>C (p.Ser1246=)
c.*1579G>C (n.*1579G>C)
c.3798G>C (p.Ser1266=)
n.3505G>C
c.4050G>C (p.Ser1350=)
c.3951G>C (p.Ser1317=)
c.4365G>C (p.Ser1455=)
dbSNP COSMIC
16g.9763335C>TCA7896198GRIN2Ac.4209G>A (p.Ser1403=)
c.*20G>A (n.*20G>A)
n.3459G>A
c.3738G>A (p.Ser1246=)
c.*1579G>A (n.*1579G>A)
c.3798G>A (p.Ser1266=)
n.3505G>A
c.4050G>A (p.Ser1350=)
c.3951G>A (p.Ser1317=)
c.4365G>A (p.Ser1455=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.9763336G>ACA394705766GRIN2Ac.4208C>T (p.Ser1403Leu)
c.*19C>T (n.*19C>T)
n.3458C>T
c.3737C>T (p.Ser1246Leu)
c.*1578C>T (n.*1578C>T)
c.3797C>T (p.Ser1266Leu)
n.3504C>T
c.4049C>T (p.Ser1350Leu)
c.3950C>T (p.Ser1317Leu)
c.4364C>T (p.Ser1455Leu)
ClinVar dbSNP gnomAD v4 COSMIC
16g.9763336G>CCA394705763GRIN2Ac.4208C>G (p.Ser1403Trp)
c.*19C>G (n.*19C>G)
n.3458C>G
c.3737C>G (p.Ser1246Trp)
c.*1578C>G (n.*1578C>G)
c.3797C>G (p.Ser1266Trp)
n.3504C>G
c.4049C>G (p.Ser1350Trp)
c.3950C>G (p.Ser1317Trp)
c.4364C>G (p.Ser1455Trp)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.9763336G=CA2206692672GRIN2Ac.4208C= (p.Ser1403=)
c.*19C= (n.*19C=)
n.3458C=
c.3737C= (p.Ser1246=)
c.*1578C= (n.*1578C=)
c.3797C= (p.Ser1266=)
n.3504C=
c.4049C= (p.Ser1350=)
c.3950C= (p.Ser1317=)
c.4364C= (p.Ser1455=)
16g.9763336G>TCA394705765GRIN2Ac.4208C>A (p.Ser1403Ter)
c.*19C>A (n.*19C>A)
n.3458C>A
c.3737C>A (p.Ser1246Ter)
c.*1578C>A (n.*1578C>A)
c.3797C>A (p.Ser1266Ter)
n.3504C>A
c.4049C>A (p.Ser1350Ter)
c.3950C>A (p.Ser1317Ter)
c.4364C>A (p.Ser1455Ter)
dbSNP
16g.9763337A>CCA394705769GRIN2Ac.4207T>G (p.Ser1403Ala)
c.*18T>G (n.*18T>G)
n.3457T>G
c.3736T>G (p.Ser1246Ala)
c.*1577T>G (n.*1577T>G)
c.3796T>G (p.Ser1266Ala)
n.3503T>G
c.4048T>G (p.Ser1350Ala)
c.3949T>G (p.Ser1317Ala)
c.4363T>G (p.Ser1455Ala)
16g.9763337A>GCA394705771GRIN2Ac.4207T>C (p.Ser1403Pro)
c.*18T>C (n.*18T>C)
n.3457T>C
c.3736T>C (p.Ser1246Pro)
c.*1577T>C (n.*1577T>C)
c.3796T>C (p.Ser1266Pro)
n.3503T>C
c.4048T>C (p.Ser1350Pro)
c.3949T>C (p.Ser1317Pro)
c.4363T>C (p.Ser1455Pro)
dbSNP gnomAD v4
16g.9763337A>TCA394705773GRIN2Ac.4207T>A (p.Ser1403Thr)
c.*18T>A (n.*18T>A)
n.3457T>A
c.3736T>A (p.Ser1246Thr)
c.*1577T>A (n.*1577T>A)
c.3796T>A (p.Ser1266Thr)
n.3503T>A
c.4048T>A (p.Ser1350Thr)
c.3949T>A (p.Ser1317Thr)
c.4363T>A (p.Ser1455Thr)
dbSNP
16g.9763338C>ACA493692483GRIN2Ac.4206G>T (p.Arg1402=)
c.*17G>T (n.*17G>T)
n.3456G>T
c.3735G>T (p.Arg1245=)
c.*1576G>T (n.*1576G>T)
c.3795G>T (p.Arg1265=)
n.3502G>T
c.4047G>T (p.Arg1349=)
c.3948G>T (p.Arg1316=)
c.4362G>T (p.Arg1454=)
ClinVar dbSNP
16g.9763338C>GCA493692484GRIN2Ac.4206G>C (p.Arg1402=)
c.*17G>C (n.*17G>C)
n.3456G>C
c.3735G>C (p.Arg1245=)
c.*1576G>C (n.*1576G>C)
c.3795G>C (p.Arg1265=)
n.3502G>C
c.4047G>C (p.Arg1349=)
c.3948G>C (p.Arg1316=)
c.4362G>C (p.Arg1454=)
dbSNP
16g.9763338C>TCA493692485GRIN2Ac.4206G>A (p.Arg1402=)
c.*17G>A (n.*17G>A)
n.3456G>A
c.3735G>A (p.Arg1245=)
c.*1576G>A (n.*1576G>A)
c.3795G>A (p.Arg1265=)
n.3502G>A
c.4047G>A (p.Arg1349=)
c.3948G>A (p.Arg1316=)
c.4362G>A (p.Arg1454=)
dbSNP
16g.9763339C>ACA394705775GRIN2Ac.4205G>T (p.Arg1402Leu)
c.*16G>T (n.*16G>T)
n.3455G>T
c.3734G>T (p.Arg1245Leu)
c.*1575G>T (n.*1575G>T)
c.3794G>T (p.Arg1265Leu)
n.3501G>T
c.4046G>T (p.Arg1349Leu)
c.3947G>T (p.Arg1316Leu)
c.4361G>T (p.Arg1454Leu)
dbSNP gnomAD v4
16g.9763339C=CA2206692673GRIN2Ac.4205G= (p.Arg1402=)
c.*16G= (n.*16G=)
n.3455G=
c.3734G= (p.Arg1245=)
c.*1575G= (n.*1575G=)
c.3794G= (p.Arg1265=)
n.3501G=
c.4046G= (p.Arg1349=)
c.3947G= (p.Arg1316=)
c.4361G= (p.Arg1454=)
16g.9763339C>GCA394705777GRIN2Ac.4205G>C (p.Arg1402Pro)
c.*16G>C (n.*16G>C)
n.3455G>C
c.3734G>C (p.Arg1245Pro)
c.*1575G>C (n.*1575G>C)
c.3794G>C (p.Arg1265Pro)
n.3501G>C
c.4046G>C (p.Arg1349Pro)
c.3947G>C (p.Arg1316Pro)
c.4361G>C (p.Arg1454Pro)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.9763339C>TCA7896199GRIN2Ac.4205G>A (p.Arg1402Gln)
c.*16G>A (n.*16G>A)
n.3455G>A
c.3734G>A (p.Arg1245Gln)
c.*1575G>A (n.*1575G>A)
c.3794G>A (p.Arg1265Gln)
n.3501G>A
c.4046G>A (p.Arg1349Gln)
c.3947G>A (p.Arg1316Gln)
c.4361G>A (p.Arg1454Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.9763340G>ACA277535958GRIN2Ac.4204C>T (p.Arg1402Trp)
c.*15C>T (n.*15C>T)
n.3454C>T
c.3733C>T (p.Arg1245Trp)
c.*1574C>T (n.*1574C>T)
c.3793C>T (p.Arg1265Trp)
n.3500C>T
c.4045C>T (p.Arg1349Trp)
c.3946C>T (p.Arg1316Trp)
c.4360C>T (p.Arg1454Trp)
dbSNP gnomAD v4 COSMIC
16g.9763340G>CCA394705781GRIN2Ac.4204C>G (p.Arg1402Gly)
c.*15C>G (n.*15C>G)
n.3454C>G
c.3733C>G (p.Arg1245Gly)
c.*1574C>G (n.*1574C>G)
c.3793C>G (p.Arg1265Gly)
n.3500C>G
c.4045C>G (p.Arg1349Gly)
c.3946C>G (p.Arg1316Gly)
c.4360C>G (p.Arg1454Gly)
dbSNP
16g.9763340G=CA2206692674GRIN2Ac.4204C= (p.Arg1402=)
c.*15C= (n.*15C=)
n.3454C=
c.3733C= (p.Arg1245=)
c.*1574C= (n.*1574C=)
c.3793C= (p.Arg1265=)
n.3500C=
c.4045C= (p.Arg1349=)
c.3946C= (p.Arg1316=)
c.4360C= (p.Arg1454=)
16g.9763340G>TCA493692489GRIN2Ac.4204C>A (p.Arg1402=)
c.*15C>A (n.*15C>A)
n.3454C>A
c.3733C>A (p.Arg1245=)
c.*1574C>A (n.*1574C>A)
c.3793C>A (p.Arg1265=)
n.3500C>A
c.4045C>A (p.Arg1349=)
c.3946C>A (p.Arg1316=)
c.4360C>A (p.Arg1454=)
gnomAD v4
16g.9763341A>CCA493692490GRIN2Ac.4203T>G (p.Leu1401=)
c.*14T>G (n.*14T>G)
n.3453T>G
c.3732T>G (p.Leu1244=)
c.*1573T>G (n.*1573T>G)
c.3792T>G (p.Leu1264=)
n.3499T>G
c.4044T>G (p.Leu1348=)
c.3945T>G (p.Leu1315=)
c.4359T>G (p.Leu1453=)
16g.9763341A>GCA493692491GRIN2Ac.4203T>C (p.Leu1401=)
c.*14T>C (n.*14T>C)
n.3453T>C
c.3732T>C (p.Leu1244=)
c.*1573T>C (n.*1573T>C)
c.3792T>C (p.Leu1264=)
n.3499T>C
c.4044T>C (p.Leu1348=)
c.3945T>C (p.Leu1315=)
c.4359T>C (p.Leu1453=)
16g.9763341A>TCA493692493GRIN2Ac.4203T>A (p.Leu1401=)
c.*14T>A (n.*14T>A)
n.3453T>A
c.3732T>A (p.Leu1244=)
c.*1573T>A (n.*1573T>A)
c.3792T>A (p.Leu1264=)
n.3499T>A
c.4044T>A (p.Leu1348=)
c.3945T>A (p.Leu1315=)
c.4359T>A (p.Leu1453=)
16g.9763342A>CCA394705784GRIN2Ac.4202T>G (p.Leu1401Arg)
c.*13T>G (n.*13T>G)
n.3452T>G
c.3731T>G (p.Leu1244Arg)
c.*1572T>G (n.*1572T>G)
c.3791T>G (p.Leu1264Arg)
n.3498T>G
c.4043T>G (p.Leu1348Arg)
c.3944T>G (p.Leu1315Arg)
c.4358T>G (p.Leu1453Arg)
COSMIC
16g.9763342A>GCA394705786GRIN2Ac.4202T>C (p.Leu1401Pro)
c.*13T>C (n.*13T>C)
n.3452T>C
c.3731T>C (p.Leu1244Pro)
c.*1572T>C (n.*1572T>C)
c.3791T>C (p.Leu1264Pro)
n.3498T>C
c.4043T>C (p.Leu1348Pro)
c.3944T>C (p.Leu1315Pro)
c.4358T>C (p.Leu1453Pro)
16g.9763342A>TCA394705788GRIN2Ac.4202T>A (p.Leu1401His)
c.*13T>A (n.*13T>A)
n.3452T>A
c.3731T>A (p.Leu1244His)
c.*1572T>A (n.*1572T>A)
c.3791T>A (p.Leu1264His)
n.3498T>A
c.4043T>A (p.Leu1348His)
c.3944T>A (p.Leu1315His)
c.4358T>A (p.Leu1453His)
dbSNP
16g.9763343G>ACA394705789GRIN2Ac.4201C>T (p.Leu1401Phe)
c.*12C>T (n.*12C>T)
n.3451C>T
c.3730C>T (p.Leu1244Phe)
c.*1571C>T (n.*1571C>T)
c.3790C>T (p.Leu1264Phe)
n.3497C>T
c.4042C>T (p.Leu1348Phe)
c.3943C>T (p.Leu1315Phe)
c.4357C>T (p.Leu1453Phe)
ClinVar dbSNP gnomAD v4
16g.9763343G>CCA394705794GRIN2Ac.4201C>G (p.Leu1401Val)
c.*12C>G (n.*12C>G)
n.3451C>G
c.3730C>G (p.Leu1244Val)
c.*1571C>G (n.*1571C>G)
c.3790C>G (p.Leu1264Val)
n.3497C>G
c.4042C>G (p.Leu1348Val)
c.3943C>G (p.Leu1315Val)
c.4357C>G (p.Leu1453Val)
dbSNP
16g.9763343G>TCA394705792GRIN2Ac.4201C>A (p.Leu1401Ile)
c.*12C>A (n.*12C>A)
n.3451C>A
c.3730C>A (p.Leu1244Ile)
c.*1571C>A (n.*1571C>A)
c.3790C>A (p.Leu1264Ile)
n.3497C>A
c.4042C>A (p.Leu1348Ile)
c.3943C>A (p.Leu1315Ile)
c.4357C>A (p.Leu1453Ile)
16g.9763344A>CCA394705796GRIN2Ac.4200T>G (p.Tyr1400Ter)
c.*11T>G (n.*11T>G)
n.3450T>G
c.3729T>G (p.Tyr1243Ter)
c.*1570T>G (n.*1570T>G)
c.3789T>G (p.Tyr1263Ter)
n.3496T>G
c.4041T>G (p.Tyr1347Ter)
c.3942T>G (p.Tyr1314Ter)
c.4356T>G (p.Tyr1452Ter)
16g.9763344A>GCA493692495GRIN2Ac.4200T>C (p.Tyr1400=)
c.*11T>C (n.*11T>C)
n.3450T>C
c.3729T>C (p.Tyr1243=)
c.*1570T>C (n.*1570T>C)
c.3789T>C (p.Tyr1263=)
n.3496T>C
c.4041T>C (p.Tyr1347=)
c.3942T>C (p.Tyr1314=)
c.4356T>C (p.Tyr1452=)
16g.9763344A>TCA394705798GRIN2Ac.4200T>A (p.Tyr1400Ter)
c.*11T>A (n.*11T>A)
n.3450T>A
c.3729T>A (p.Tyr1243Ter)
c.*1570T>A (n.*1570T>A)
c.3789T>A (p.Tyr1263Ter)
n.3496T>A
c.4041T>A (p.Tyr1347Ter)
c.3942T>A (p.Tyr1314Ter)
c.4356T>A (p.Tyr1452Ter)
dbSNP
16g.9763345T>ACA394705800GRIN2Ac.4199A>T (p.Tyr1400Phe)
c.*10A>T (n.*10A>T)
n.3449A>T
c.3728A>T (p.Tyr1243Phe)
c.*1569A>T (n.*1569A>T)
c.3788A>T (p.Tyr1263Phe)
n.3495A>T
c.4040A>T (p.Tyr1347Phe)
c.3941A>T (p.Tyr1314Phe)
c.4355A>T (p.Tyr1452Phe)
dbSNP
16g.9763345T>CCA394705802GRIN2Ac.4199A>G (p.Tyr1400Cys)
c.*10A>G (n.*10A>G)
n.3449A>G
c.3728A>G (p.Tyr1243Cys)
c.*1569A>G (n.*1569A>G)
c.3788A>G (p.Tyr1263Cys)
n.3495A>G
c.4040A>G (p.Tyr1347Cys)
c.3941A>G (p.Tyr1314Cys)
c.4355A>G (p.Tyr1452Cys)
dbSNP gnomAD v4
16g.9763345T>GCA394705804GRIN2Ac.4199A>C (p.Tyr1400Ser)
c.*10A>C (n.*10A>C)
n.3449A>C
c.3728A>C (p.Tyr1243Ser)
c.*1569A>C (n.*1569A>C)
c.3788A>C (p.Tyr1263Ser)
n.3495A>C
c.4040A>C (p.Tyr1347Ser)
c.3941A>C (p.Tyr1314Ser)
c.4355A>C (p.Tyr1452Ser)
dbSNP
16g.9763345T=CA2206692675GRIN2Ac.4199A= (p.Tyr1400=)
c.*10A= (n.*10A=)
n.3449A=
c.3728A= (p.Tyr1243=)
c.*1569A= (n.*1569A=)
c.3788A= (p.Tyr1263=)
n.3495A=
c.4040A= (p.Tyr1347=)
c.3941A= (p.Tyr1314=)
c.4355A= (p.Tyr1452=)
16g.9763346A>CCA394705807GRIN2Ac.4198T>G (p.Tyr1400Asp)
c.*9T>G (n.*9T>G)
n.3448T>G
c.3727T>G (p.Tyr1243Asp)
c.*1568T>G (n.*1568T>G)
c.3787T>G (p.Tyr1263Asp)
n.3494T>G
c.4039T>G (p.Tyr1347Asp)
c.3940T>G (p.Tyr1314Asp)
c.4354T>G (p.Tyr1452Asp)
16g.9763346A>GCA394705808GRIN2Ac.4198T>C (p.Tyr1400His)
c.*9T>C (n.*9T>C)
n.3448T>C
c.3727T>C (p.Tyr1243His)
c.*1568T>C (n.*1568T>C)
c.3787T>C (p.Tyr1263His)
n.3494T>C
c.4039T>C (p.Tyr1347His)
c.3940T>C (p.Tyr1314His)
c.4354T>C (p.Tyr1452His)
ClinVar
16g.9763346A>TCA394705809GRIN2Ac.4198T>A (p.Tyr1400Asn)
c.*9T>A (n.*9T>A)
n.3448T>A
c.3727T>A (p.Tyr1243Asn)
c.*1568T>A (n.*1568T>A)
c.3787T>A (p.Tyr1263Asn)
n.3494T>A
c.4039T>A (p.Tyr1347Asn)
c.3940T>A (p.Tyr1314Asn)
c.4354T>A (p.Tyr1452Asn)
dbSNP
16g.9763347G>ACA493692502GRIN2Ac.4197C>T (p.Ser1399=)
c.*8C>T (n.*8C>T)
n.3447C>T
c.3726C>T (p.Ser1242=)
c.*1567C>T (n.*1567C>T)
c.3786C>T (p.Ser1262=)
n.3493C>T
c.4038C>T (p.Ser1346=)
c.3939C>T (p.Ser1313=)
c.4353C>T (p.Ser1451=)
dbSNP COSMIC
16g.9763347G>CCA394705812GRIN2Ac.4197C>G (p.Ser1399Arg)
c.*8C>G (n.*8C>G)
n.3447C>G
c.3726C>G (p.Ser1242Arg)
c.*1567C>G (n.*1567C>G)
c.3786C>G (p.Ser1262Arg)
n.3493C>G
c.4038C>G (p.Ser1346Arg)
c.3939C>G (p.Ser1313Arg)
c.4353C>G (p.Ser1451Arg)
dbSNP
16g.9763347G>TCA394705814GRIN2Ac.4197C>A (p.Ser1399Arg)
c.*8C>A (n.*8C>A)
n.3447C>A
c.3726C>A (p.Ser1242Arg)
c.*1567C>A (n.*1567C>A)
c.3786C>A (p.Ser1262Arg)
n.3493C>A
c.4038C>A (p.Ser1346Arg)
c.3939C>A (p.Ser1313Arg)
c.4353C>A (p.Ser1451Arg)
16g.9763348C>ACA394705819GRIN2Ac.4196G>T (p.Ser1399Ile)
c.*7G>T (n.*7G>T)
n.3446G>T
c.3725G>T (p.Ser1242Ile)
c.*1566G>T (n.*1566G>T)
c.3785G>T (p.Ser1262Ile)
n.3492G>T
c.4037G>T (p.Ser1346Ile)
c.3938G>T (p.Ser1313Ile)
c.4352G>T (p.Ser1451Ile)
dbSNP
16g.9763348C=CA2206692676GRIN2Ac.4196G= (p.Ser1399=)
c.*7G= (n.*7G=)
n.3446G=
c.3725G= (p.Ser1242=)
c.*1566G= (n.*1566G=)
c.3785G= (p.Ser1262=)
n.3492G=
c.4037G= (p.Ser1346=)
c.3938G= (p.Ser1313=)
c.4352G= (p.Ser1451=)
16g.9763348C>GCA394705817GRIN2Ac.4196G>C (p.Ser1399Thr)
c.*7G>C (n.*7G>C)
n.3446G>C
c.3725G>C (p.Ser1242Thr)
c.*1566G>C (n.*1566G>C)
c.3785G>C (p.Ser1262Thr)
n.3492G>C
c.4037G>C (p.Ser1346Thr)
c.3938G>C (p.Ser1313Thr)
c.4352G>C (p.Ser1451Thr)
dbSNP
16g.9763348C>TCA394705815GRIN2Ac.4196G>A (p.Ser1399Asn)
c.*7G>A (n.*7G>A)
n.3446G>A
c.3725G>A (p.Ser1242Asn)
c.*1566G>A (n.*1566G>A)
c.3785G>A (p.Ser1262Asn)
n.3492G>A
c.4037G>A (p.Ser1346Asn)
c.3938G>A (p.Ser1313Asn)
c.4352G>A (p.Ser1451Asn)
dbSNP
16g.9763349T>ACA394705821GRIN2Ac.4195A>T (p.Ser1399Cys)
c.*6A>T (n.*6A>T)
n.3445A>T
c.3724A>T (p.Ser1242Cys)
c.*1565A>T (n.*1565A>T)
c.3784A>T (p.Ser1262Cys)
n.3491A>T
c.4036A>T (p.Ser1346Cys)
c.3937A>T (p.Ser1313Cys)
c.4351A>T (p.Ser1451Cys)
dbSNP
16g.9763349T>CCA394705823GRIN2Ac.4195A>G (p.Ser1399Gly)
c.*6A>G (n.*6A>G)
n.3445A>G
c.3724A>G (p.Ser1242Gly)
c.*1565A>G (n.*1565A>G)
c.3784A>G (p.Ser1262Gly)
n.3491A>G
c.4036A>G (p.Ser1346Gly)
c.3937A>G (p.Ser1313Gly)
c.4351A>G (p.Ser1451Gly)
ClinVar dbSNP gnomAD v4
16g.9763349T>GCA394705825GRIN2Ac.4195A>C (p.Ser1399Arg)
c.*6A>C (n.*6A>C)
n.3445A>C
c.3724A>C (p.Ser1242Arg)
c.*1565A>C (n.*1565A>C)
c.3784A>C (p.Ser1262Arg)
n.3491A>C
c.4036A>C (p.Ser1346Arg)
c.3937A>C (p.Ser1313Arg)
c.4351A>C (p.Ser1451Arg)
16g.9763349T=CA2206692677GRIN2Ac.4195A= (p.Ser1399=)
c.*6A= (n.*6A=)
n.3445A=
c.3724A= (p.Ser1242=)
c.*1565A= (n.*1565A=)
c.3784A= (p.Ser1262=)
n.3491A=
c.4036A= (p.Ser1346=)
c.3937A= (p.Ser1313=)
c.4351A= (p.Ser1451=)
16g.9763350G>ACA493692509GRIN2Ac.4194C>T (p.Asp1398=)
c.*5C>T (n.*5C>T)
n.3444C>T
c.3723C>T (p.Asp1241=)
c.*1564C>T (n.*1564C>T)
c.3783C>T (p.Asp1261=)
n.3490C>T
c.4035C>T (p.Asp1345=)
c.3936C>T (p.Asp1312=)
c.4350C>T (p.Asp1450=)
dbSNP gnomAD v3 gnomAD v4
16g.9763350G>CCA394705827GRIN2Ac.4194C>G (p.Asp1398Glu)
c.*5C>G (n.*5C>G)
n.3444C>G
c.3723C>G (p.Asp1241Glu)
c.*1564C>G (n.*1564C>G)
c.3783C>G (p.Asp1261Glu)
n.3490C>G
c.4035C>G (p.Asp1345Glu)
c.3936C>G (p.Asp1312Glu)
c.4350C>G (p.Asp1450Glu)
dbSNP
16g.9763350G=CA2206692678GRIN2Ac.4194C= (p.Asp1398=)
c.*5C= (n.*5C=)
n.3444C=
c.3723C= (p.Asp1241=)
c.*1564C= (n.*1564C=)
c.3783C= (p.Asp1261=)
n.3490C=
c.4035C= (p.Asp1345=)
c.3936C= (p.Asp1312=)
c.4350C= (p.Asp1450=)
16g.9763350G>TCA394705829GRIN2Ac.4194C>A (p.Asp1398Glu)
c.*5C>A (n.*5C>A)
n.3444C>A
c.3723C>A (p.Asp1241Glu)
c.*1564C>A (n.*1564C>A)
c.3783C>A (p.Asp1261Glu)
n.3490C>A
c.4035C>A (p.Asp1345Glu)
c.3936C>A (p.Asp1312Glu)
c.4350C>A (p.Asp1450Glu)
16g.9763351T>ACA394705831GRIN2Ac.4193A>T (p.Asp1398Val)
c.*4A>T (n.*4A>T)
n.3443A>T
c.3722A>T (p.Asp1241Val)
c.*1563A>T (n.*1563A>T)
c.3782A>T (p.Asp1261Val)
n.3489A>T
c.4034A>T (p.Asp1345Val)
c.3935A>T (p.Asp1312Val)
c.4349A>T (p.Asp1450Val)
dbSNP
16g.9763351T>CCA394705833GRIN2Ac.4193A>G (p.Asp1398Gly)
c.*4A>G (n.*4A>G)
n.3443A>G
c.3722A>G (p.Asp1241Gly)
c.*1563A>G (n.*1563A>G)
c.3782A>G (p.Asp1261Gly)
n.3489A>G
c.4034A>G (p.Asp1345Gly)
c.3935A>G (p.Asp1312Gly)
c.4349A>G (p.Asp1450Gly)
dbSNP
16g.9763351T>GCA394705835GRIN2Ac.4193A>C (p.Asp1398Ala)
c.*4A>C (n.*4A>C)
n.3443A>C
c.3722A>C (p.Asp1241Ala)
c.*1563A>C (n.*1563A>C)
c.3782A>C (p.Asp1261Ala)
n.3489A>C
c.4034A>C (p.Asp1345Ala)
c.3935A>C (p.Asp1312Ala)
c.4349A>C (p.Asp1450Ala)
dbSNP
16g.9763351_9763355delCA2695222771GRIN2Ac.4189_4193del (p.Asn1397GlnfsTer23)
c.3375_*4del (n.[c.3375_*4del;Ter1125CysextTer?])
n.3439_3443del
c.3718_3722del (p.Asn1240GlnfsTer23)
c.*1559_*1563del (n.*1559_*1563del)
c.3778_3782del (p.Asn1260GlnfsTer23)
n.3485_3489del
c.3435_*4del (n.[c.3435_*4del;Ter1145CysextTer?])
c.3846_*4del (n.[c.3846_*4del;Ter1282CysextTer?])
c.4030_4034del (p.Asn1344GlnfsTer23)
c.3931_3935del (p.Asn1311GlnfsTer23)
c.4345_4349del (p.Asn1449GlnfsTer23)
c.4002_*4del (n.[c.4002_*4del;Ter1334CysextTer?])
16g.9763354_9763357delCA2631674844GRIN2Ac.4190_4193del (p.Asn1397ThrfsTer8)
c.*1_*4del (n.*1_*4del)
n.3440_3443del
c.3719_3722del (p.Asn1240ThrfsTer8)
c.*1560_*1563del (n.*1560_*1563del)
c.3779_3782del (p.Asn1260ThrfsTer8)
n.3486_3489del
c.4031_4034del (p.Asn1344ThrfsTer8)
c.3932_3935del (p.Asn1311ThrfsTer8)
c.4346_4349del (p.Asn1449ThrfsTer8)
gnomAD v4
16g.9763352C>ACA394705837GRIN2Ac.4192G>T (p.Asp1398Tyr)
c.*3G>T (n.*3G>T)
n.3442G>T
c.3721G>T (p.Asp1241Tyr)
c.*1562G>T (n.*1562G>T)
c.3781G>T (p.Asp1261Tyr)
n.3488G>T
c.4033G>T (p.Asp1345Tyr)
c.3934G>T (p.Asp1312Tyr)
c.4348G>T (p.Asp1450Tyr)
16g.9763352C>GCA394705839GRIN2Ac.4192G>C (p.Asp1398His)
c.*3G>C (n.*3G>C)
n.3442G>C
c.3721G>C (p.Asp1241His)
c.*1562G>C (n.*1562G>C)
c.3781G>C (p.Asp1261His)
n.3488G>C
c.4033G>C (p.Asp1345His)
c.3934G>C (p.Asp1312His)
c.4348G>C (p.Asp1450His)
dbSNP
16g.9763352C>TCA394705841GRIN2Ac.4192G>A (p.Asp1398Asn)
c.*3G>A (n.*3G>A)
n.3442G>A
c.3721G>A (p.Asp1241Asn)
c.*1562G>A (n.*1562G>A)
c.3781G>A (p.Asp1261Asn)
n.3488G>A
c.4033G>A (p.Asp1345Asn)
c.3934G>A (p.Asp1312Asn)
c.4348G>A (p.Asp1450Asn)
dbSNP
16g.9763353A=CA2206692679GRIN2Ac.4191T= (p.Asn1397=)
c.*2T= (n.*2T=)
n.3441T=
c.3720T= (p.Asn1240=)
c.*1561T= (n.*1561T=)
c.3780T= (p.Asn1260=)
n.3487T=
c.4032T= (p.Asn1344=)
c.3933T= (p.Asn1311=)
c.4347T= (p.Asn1449=)
16g.9763353A>CCA394705843GRIN2Ac.4191T>G (p.Asn1397Lys)
c.*2T>G (n.*2T>G)
n.3441T>G
c.3720T>G (p.Asn1240Lys)
c.*1561T>G (n.*1561T>G)
c.3780T>G (p.Asn1260Lys)
n.3487T>G
c.4032T>G (p.Asn1344Lys)
c.3933T>G (p.Asn1311Lys)
c.4347T>G (p.Asn1449Lys)
16g.9763353A>GCA493692511GRIN2Ac.4191T>C (p.Asn1397=)
c.*2T>C (n.*2T>C)
n.3441T>C
c.3720T>C (p.Asn1240=)
c.*1561T>C (n.*1561T>C)
c.3780T>C (p.Asn1260=)
n.3487T>C
c.4032T>C (p.Asn1344=)
c.3933T>C (p.Asn1311=)
c.4347T>C (p.Asn1449=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.9763353A>TCA394705844GRIN2Ac.4191T>A (p.Asn1397Lys)
c.*2T>A (n.*2T>A)
n.3441T>A
c.3720T>A (p.Asn1240Lys)
c.*1561T>A (n.*1561T>A)
c.3780T>A (p.Asn1260Lys)
n.3487T>A
c.4032T>A (p.Asn1344Lys)
c.3933T>A (p.Asn1311Lys)
c.4347T>A (p.Asn1449Lys)
dbSNP
16g.9763354T>ACA394705850GRIN2Ac.4190A>T (p.Asn1397Ile)
c.*1A>T (n.*1A>T)
n.3440A>T
c.3719A>T (p.Asn1240Ile)
c.*1560A>T (n.*1560A>T)
c.3779A>T (p.Asn1260Ile)
n.3486A>T
c.4031A>T (p.Asn1344Ile)
c.3932A>T (p.Asn1311Ile)
c.4346A>T (p.Asn1449Ile)
dbSNP
16g.9763354T>CCA394705847GRIN2Ac.4190A>G (p.Asn1397Ser)
c.*1A>G (n.*1A>G)
n.3440A>G
c.3719A>G (p.Asn1240Ser)
c.*1560A>G (n.*1560A>G)
c.3779A>G (p.Asn1260Ser)
n.3486A>G
c.4031A>G (p.Asn1344Ser)
c.3932A>G (p.Asn1311Ser)
c.4346A>G (p.Asn1449Ser)
dbSNP
16g.9763354T>GCA394705849GRIN2Ac.4190A>C (p.Asn1397Thr)
c.*1A>C (n.*1A>C)
n.3440A>C
c.3719A>C (p.Asn1240Thr)
c.*1560A>C (n.*1560A>C)
c.3779A>C (p.Asn1260Thr)
n.3486A>C
c.4031A>C (p.Asn1344Thr)
c.3932A>C (p.Asn1311Thr)
c.4346A>C (p.Asn1449Thr)
dbSNP
16g.9763355T>ACA394705853GRIN2Ac.4189A>T (p.Asn1397Tyr)
c.3375A>T (p.Ter1125Cys)
n.3439A>T
c.3718A>T (p.Asn1240Tyr)
c.*1559A>T (n.*1559A>T)
c.3778A>T (p.Asn1260Tyr)
n.3485A>T
c.3435A>T (p.Ter1145Cys)
c.3846A>T (p.Ter1282Cys)
c.4030A>T (p.Asn1344Tyr)
c.3931A>T (p.Asn1311Tyr)
c.4345A>T (p.Asn1449Tyr)
c.4002A>T (p.Ter1334Cys)
16g.9763355T>CCA394705855GRIN2Ac.4189A>G (p.Asn1397Asp)
c.3375A>G (p.Ter1125Trp)
n.3439A>G
c.3718A>G (p.Asn1240Asp)
c.*1559A>G (n.*1559A>G)
c.3778A>G (p.Asn1260Asp)
n.3485A>G
c.3435A>G (p.Ter1145Trp)
c.3846A>G (p.Ter1282Trp)
c.4030A>G (p.Asn1344Asp)
c.3931A>G (p.Asn1311Asp)
c.4345A>G (p.Asn1449Asp)
c.4002A>G (p.Ter1334Trp)
dbSNP
16g.9763355T>GCA394705857GRIN2Ac.4189A>C (p.Asn1397His)
c.3375A>C (p.Ter1125Cys)
n.3439A>C
c.3718A>C (p.Asn1240His)
c.*1559A>C (n.*1559A>C)
c.3778A>C (p.Asn1260His)
n.3485A>C
c.3435A>C (p.Ter1145Cys)
c.3846A>C (p.Ter1282Cys)
c.4030A>C (p.Asn1344His)
c.3931A>C (p.Asn1311His)
c.4345A>C (p.Asn1449His)
c.4002A>C (p.Ter1334Cys)
16g.9763356C>ACA394705859GRIN2Ac.4188G>T (p.Val1396=)
c.3374G>T (p.Ter1125Leu)
n.3438G>T
c.3717G>T (p.Val1239=)
c.*1558G>T (n.*1558G>T)
c.3777G>T (p.Val1259=)
n.3484G>T
c.3434G>T (p.Ter1145Leu)
c.3845G>T (p.Ter1282Leu)
c.4029G>T (p.Val1343=)
c.3930G>T (p.Val1310=)
c.4344G>T (p.Val1448=)
c.4001G>T (p.Ter1334Leu)
16g.9763356C=CA2206692680GRIN2Ac.4188G= (p.Val1396=)
c.3374G= (p.Ter1125=)
n.3438G=
c.3717G= (p.Val1239=)
c.*1558G= (n.*1558G=)
c.3777G= (p.Val1259=)
n.3484G=
c.3434G= (p.Ter1145=)
c.3845G= (p.Ter1282=)
c.4029G= (p.Val1343=)
c.3930G= (p.Val1310=)
c.4344G= (p.Val1448=)
c.4001G= (p.Ter1334=)
16g.9763356C>GCA394705860GRIN2Ac.4188G>C (p.Val1396=)
c.3374G>C (p.Ter1125Ser)
n.3438G>C
c.3717G>C (p.Val1239=)
c.*1558G>C (n.*1558G>C)
c.3777G>C (p.Val1259=)
n.3484G>C
c.3434G>C (p.Ter1145Ser)
c.3845G>C (p.Ter1282Ser)
c.4029G>C (p.Val1343=)
c.3930G>C (p.Val1310=)
c.4344G>C (p.Val1448=)
c.4001G>C (p.Ter1334Ser)
dbSNP
16g.9763356C>TCA7896200GRIN2Ac.4188G>A (p.Val1396=)
c.3374G>A (p.Ter1125=)
n.3438G>A
c.3717G>A (p.Val1239=)
c.*1558G>A (n.*1558G>A)
c.3777G>A (p.Val1259=)
n.3484G>A
c.3434G>A (p.Ter1145=)
c.3845G>A (p.Ter1282=)
c.4029G>A (p.Val1343=)
c.3930G>A (p.Val1310=)
c.4344G>A (p.Val1448=)
c.4001G>A (p.Ter1334=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.9763357A>CCA394705864GRIN2Ac.4187T>G (p.Val1396Gly)
c.3373T>G (p.Ter1125Gly)
n.3437T>G
c.3716T>G (p.Val1239Gly)
c.*1557T>G (n.*1557T>G)
c.3776T>G (p.Val1259Gly)
n.3483T>G
c.3433T>G (p.Ter1145Gly)
c.3844T>G (p.Ter1282Gly)
c.4028T>G (p.Val1343Gly)
c.3929T>G (p.Val1310Gly)
c.4343T>G (p.Val1448Gly)
c.4000T>G (p.Ter1334Gly)
16g.9763357A>GCA394705867GRIN2Ac.4187T>C (p.Val1396Ala)
c.3373T>C (p.Ter1125Arg)
n.3437T>C
c.3716T>C (p.Val1239Ala)
c.*1557T>C (n.*1557T>C)
c.3776T>C (p.Val1259Ala)
n.3483T>C
c.3433T>C (p.Ter1145Arg)
c.3844T>C (p.Ter1282Arg)
c.4028T>C (p.Val1343Ala)
c.3929T>C (p.Val1310Ala)
c.4343T>C (p.Val1448Ala)
c.4000T>C (p.Ter1334Arg)
dbSNP
16g.9763357A>TCA394705869GRIN2Ac.4187T>A (p.Val1396Glu)
c.3373T>A (p.Ter1125Arg)
n.3437T>A
c.3716T>A (p.Val1239Glu)
c.*1557T>A (n.*1557T>A)
c.3776T>A (p.Val1259Glu)
n.3483T>A
c.3433T>A (p.Ter1145Arg)
c.3844T>A (p.Ter1282Arg)
c.4028T>A (p.Val1343Glu)
c.3929T>A (p.Val1310Glu)
c.4343T>A (p.Val1448Glu)
c.4000T>A (p.Ter1334Arg)
dbSNP
16g.9763358C>ACA394705872GRIN2Ac.4186G>T (p.Val1396Leu)
c.3372G>T (p.Arg1124=)
n.3436G>T
c.3715G>T (p.Val1239Leu)
c.*1556G>T (n.*1556G>T)
c.3775G>T (p.Val1259Leu)
n.3482G>T
c.3432G>T (p.Arg1144=)
c.3843G>T (p.Arg1281=)
c.4027G>T (p.Val1343Leu)
c.3928G>T (p.Val1310Leu)
c.4342G>T (p.Val1448Leu)
c.3999G>T (p.Arg1333=)
16g.9763358C=CA2206692681GRIN2Ac.4186G= (p.Val1396=)
c.3372G= (p.Arg1124=)
n.3436G=
c.3715G= (p.Val1239=)
c.*1556G= (n.*1556G=)
c.3775G= (p.Val1259=)
n.3482G=
c.3432G= (p.Arg1144=)
c.3843G= (p.Arg1281=)
c.4027G= (p.Val1343=)
c.3928G= (p.Val1310=)
c.4342G= (p.Val1448=)
c.3999G= (p.Arg1333=)
16g.9763358C>GCA394705874GRIN2Ac.4186G>C (p.Val1396Leu)
c.3372G>C (p.Arg1124=)
n.3436G>C
c.3715G>C (p.Val1239Leu)
c.*1556G>C (n.*1556G>C)
c.3775G>C (p.Val1259Leu)
n.3482G>C
c.3432G>C (p.Arg1144=)
c.3843G>C (p.Arg1281=)
c.4027G>C (p.Val1343Leu)
c.3928G>C (p.Val1310Leu)
c.4342G>C (p.Val1448Leu)
c.3999G>C (p.Arg1333=)
dbSNP
16g.9763358C>TCA394705876GRIN2Ac.4186G>A (p.Val1396Met)
c.3372G>A (p.Arg1124=)
n.3436G>A
c.3715G>A (p.Val1239Met)
c.*1556G>A (n.*1556G>A)
c.3775G>A (p.Val1259Met)
n.3482G>A
c.3432G>A (p.Arg1144=)
c.3843G>A (p.Arg1281=)
c.4027G>A (p.Val1343Met)
c.3928G>A (p.Val1310Met)
c.4342G>A (p.Val1448Met)
c.3999G>A (p.Arg1333=)
dbSNP gnomAD v2 gnomAD v4
16g.9763359C>ACA394705879GRIN2Ac.4185G>T (p.Ala1395=)
c.3371G>T (p.Arg1124Leu)
n.3435G>T
c.3714G>T (p.Ala1238=)
c.*1555G>T (n.*1555G>T)
c.3774G>T (p.Ala1258=)
n.3481G>T
c.3431G>T (p.Arg1144Leu)
c.3842G>T (p.Arg1281Leu)
c.4026G>T (p.Ala1342=)
c.3927G>T (p.Ala1309=)
c.4341G>T (p.Ala1447=)
c.3998G>T (p.Arg1333Leu)
dbSNP gnomAD v4
16g.9763359C=CA2206692682GRIN2Ac.4185G= (p.Ala1395=)
c.3371G= (p.Arg1124=)
n.3435G=
c.3714G= (p.Ala1238=)
c.*1555G= (n.*1555G=)
c.3774G= (p.Ala1258=)
n.3481G=
c.3431G= (p.Arg1144=)
c.3842G= (p.Arg1281=)
c.4026G= (p.Ala1342=)
c.3927G= (p.Ala1309=)
c.4341G= (p.Ala1447=)
c.3998G= (p.Arg1333=)
16g.9763359C>GCA394705878GRIN2Ac.4185G>C (p.Ala1395=)
c.3371G>C (p.Arg1124Pro)
n.3435G>C
c.3714G>C (p.Ala1238=)
c.*1555G>C (n.*1555G>C)
c.3774G>C (p.Ala1258=)
n.3481G>C
c.3431G>C (p.Arg1144Pro)
c.3842G>C (p.Arg1281Pro)
c.4026G>C (p.Ala1342=)
c.3927G>C (p.Ala1309=)
c.4341G>C (p.Ala1447=)
c.3998G>C (p.Arg1333Pro)
dbSNP
16g.9763359C>TCA7896201GRIN2Ac.4185G>A (p.Ala1395=)
c.3371G>A (p.Arg1124Gln)
n.3435G>A
c.3714G>A (p.Ala1238=)
c.*1555G>A (n.*1555G>A)
c.3774G>A (p.Ala1258=)
n.3481G>A
c.3431G>A (p.Arg1144Gln)
c.3842G>A (p.Arg1281Gln)
c.4026G>A (p.Ala1342=)
c.3927G>A (p.Ala1309=)
c.4341G>A (p.Ala1447=)
c.3998G>A (p.Arg1333Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.9763360G>ACA7896202GRIN2Ac.4184C>T (p.Ala1395Val)
c.3370C>T (p.Arg1124Trp)
n.3434C>T
c.3713C>T (p.Ala1238Val)
c.*1554C>T (n.*1554C>T)
c.3773C>T (p.Ala1258Val)
n.3480C>T
c.3430C>T (p.Arg1144Trp)
c.3841C>T (p.Arg1281Trp)
c.4025C>T (p.Ala1342Val)
c.3926C>T (p.Ala1309Val)
c.4340C>T (p.Ala1447Val)
c.3997C>T (p.Arg1333Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.9763360G>CCA394705880GRIN2Ac.4184C>G (p.Ala1395Gly)
c.3370C>G (p.Arg1124Gly)
n.3434C>G
c.3713C>G (p.Ala1238Gly)
c.*1554C>G (n.*1554C>G)
c.3773C>G (p.Ala1258Gly)
n.3480C>G
c.3430C>G (p.Arg1144Gly)
c.3841C>G (p.Arg1281Gly)
c.4025C>G (p.Ala1342Gly)
c.3926C>G (p.Ala1309Gly)
c.4340C>G (p.Ala1447Gly)
c.3997C>G (p.Arg1333Gly)
dbSNP gnomAD v4
16g.9763360G=CA2206692683GRIN2Ac.4184C= (p.Ala1395=)
c.3370C= (p.Arg1124=)
n.3434C=
c.3713C= (p.Ala1238=)
c.*1554C= (n.*1554C=)
c.3773C= (p.Ala1258=)
n.3480C=
c.3430C= (p.Arg1144=)
c.3841C= (p.Arg1281=)
c.4025C= (p.Ala1342=)
c.3926C= (p.Ala1309=)
c.4340C= (p.Ala1447=)
c.3997C= (p.Arg1333=)
16g.9763360G>TCA394705881GRIN2Ac.4184C>A (p.Ala1395Glu)
c.3370C>A (p.Arg1124=)
n.3434C>A
c.3713C>A (p.Ala1238Glu)
c.*1554C>A (n.*1554C>A)
c.3773C>A (p.Ala1258Glu)
n.3480C>A
c.3430C>A (p.Arg1144=)
c.3841C>A (p.Arg1281=)
c.4025C>A (p.Ala1342Glu)
c.3926C>A (p.Ala1309Glu)
c.4340C>A (p.Ala1447Glu)
c.3997C>A (p.Arg1333=)
ClinVar dbSNP gnomAD v2 gnomAD v4
16g.9763361C>ACA394705882GRIN2Ac.4183G>T (p.Ala1395Ser)
c.3369G>T (p.Arg1123Ser)
n.3433G>T
c.3712G>T (p.Ala1238Ser)
c.*1553G>T (n.*1553G>T)
c.3772G>T (p.Ala1258Ser)
n.3479G>T
c.3429G>T (p.Arg1143Ser)
c.3840G>T (p.Arg1280Ser)
c.4024G>T (p.Ala1342Ser)
c.3925G>T (p.Ala1309Ser)
c.4339G>T (p.Ala1447Ser)
c.3996G>T (p.Arg1332Ser)
16g.9763361C>GCA394705883GRIN2Ac.4183G>C (p.Ala1395Pro)
c.3369G>C (p.Arg1123Ser)
n.3433G>C
c.3712G>C (p.Ala1238Pro)
c.*1553G>C (n.*1553G>C)
c.3772G>C (p.Ala1258Pro)
n.3479G>C
c.3429G>C (p.Arg1143Ser)
c.3840G>C (p.Arg1280Ser)
c.4024G>C (p.Ala1342Pro)
c.3925G>C (p.Ala1309Pro)
c.4339G>C (p.Ala1447Pro)
c.3996G>C (p.Arg1332Ser)
dbSNP
16g.9763361C>TCA394705884GRIN2Ac.4183G>A (p.Ala1395Thr)
c.3369G>A (p.Arg1123=)
n.3433G>A
c.3712G>A (p.Ala1238Thr)
c.*1553G>A (n.*1553G>A)
c.3772G>A (p.Ala1258Thr)
n.3479G>A
c.3429G>A (p.Arg1143=)
c.3840G>A (p.Arg1280=)
c.4024G>A (p.Ala1342Thr)
c.3925G>A (p.Ala1309Thr)
c.4339G>A (p.Ala1447Thr)
c.3996G>A (p.Arg1332=)
ClinVar
16g.9763362C>ACA394705885GRIN2Ac.4182G>T (p.Gln1394His)
c.3368G>T (p.Arg1123Met)
n.3432G>T
c.3711G>T (p.Gln1237His)
c.*1552G>T (n.*1552G>T)
c.3771G>T (p.Gln1257His)
n.3478G>T
c.3428G>T (p.Arg1143Met)
c.3839G>T (p.Arg1280Met)
c.4023G>T (p.Gln1341His)
c.3924G>T (p.Gln1308His)
c.4338G>T (p.Gln1446His)
c.3995G>T (p.Arg1332Met)
16g.9763362C>GCA394705886GRIN2Ac.4182G>C (p.Gln1394His)
c.3368G>C (p.Arg1123Thr)
n.3432G>C
c.3711G>C (p.Gln1237His)
c.*1552G>C (n.*1552G>C)
c.3771G>C (p.Gln1257His)
n.3478G>C
c.3428G>C (p.Arg1143Thr)
c.3839G>C (p.Arg1280Thr)
c.4023G>C (p.Gln1341His)
c.3924G>C (p.Gln1308His)
c.4338G>C (p.Gln1446His)
c.3995G>C (p.Arg1332Thr)
16g.9763362C>TCA394705887GRIN2Ac.4182G>A (p.Gln1394=)
c.3368G>A (p.Arg1123Lys)
n.3432G>A
c.3711G>A (p.Gln1237=)
c.*1552G>A (n.*1552G>A)
c.3771G>A (p.Gln1257=)
n.3478G>A
c.3428G>A (p.Arg1143Lys)
c.3839G>A (p.Arg1280Lys)
c.4023G>A (p.Gln1341=)
c.3924G>A (p.Gln1308=)
c.4338G>A (p.Gln1446=)
c.3995G>A (p.Arg1332Lys)
dbSNP gnomAD v4
16g.9763363T>ACA394705888GRIN2Ac.4181A>T (p.Gln1394Leu)
c.3367A>T (p.Arg1123Trp)
n.3431A>T
c.3710A>T (p.Gln1237Leu)
c.*1551A>T (n.*1551A>T)
c.3770A>T (p.Gln1257Leu)
n.3477A>T
c.3427A>T (p.Arg1143Trp)
c.3838A>T (p.Arg1280Trp)
c.4022A>T (p.Gln1341Leu)
c.3923A>T (p.Gln1308Leu)
c.4337A>T (p.Gln1446Leu)
c.3994A>T (p.Arg1332Trp)
COSMIC
16g.9763363T>CCA394705889GRIN2Ac.4181A>G (p.Gln1394Arg)
c.3367A>G (p.Arg1123Gly)
n.3431A>G
c.3710A>G (p.Gln1237Arg)
c.*1551A>G (n.*1551A>G)
c.3770A>G (p.Gln1257Arg)
n.3477A>G
c.3427A>G (p.Arg1143Gly)
c.3838A>G (p.Arg1280Gly)
c.4022A>G (p.Gln1341Arg)
c.3923A>G (p.Gln1308Arg)
c.4337A>G (p.Gln1446Arg)
c.3994A>G (p.Arg1332Gly)
16g.9763363T>GCA394705890GRIN2Ac.4181A>C (p.Gln1394Pro)
c.3367A>C (p.Arg1123=)
n.3431A>C
c.3710A>C (p.Gln1237Pro)
c.*1551A>C (n.*1551A>C)
c.3770A>C (p.Gln1257Pro)
n.3477A>C
c.3427A>C (p.Arg1143=)
c.3838A>C (p.Arg1280=)
c.4022A>C (p.Gln1341Pro)
c.3923A>C (p.Gln1308Pro)
c.4337A>C (p.Gln1446Pro)
c.3994A>C (p.Arg1332=)
dbSNP gnomAD v3 gnomAD v4
16g.9763363T=CA2206692684GRIN2Ac.4181A= (p.Gln1394=)
c.3367A= (p.Arg1123=)
n.3431A=
c.3710A= (p.Gln1237=)
c.*1551A= (n.*1551A=)
c.3770A= (p.Gln1257=)
n.3477A=
c.3427A= (p.Arg1143=)
c.3838A= (p.Arg1280=)
c.4022A= (p.Gln1341=)
c.3923A= (p.Gln1308=)
c.4337A= (p.Gln1446=)
c.3994A= (p.Arg1332=)
16g.9763364G>ACA394705891GRIN2Ac.4180C>T (p.Gln1394Ter)
c.3366C>T (p.Pro1122=)
n.3430C>T
c.3709C>T (p.Gln1237Ter)
c.*1550C>T (n.*1550C>T)
c.3769C>T (p.Gln1257Ter)
n.3476C>T
c.3426C>T (p.Pro1142=)
c.3837C>T (p.Pro1279=)
c.4021C>T (p.Gln1341Ter)
c.3922C>T (p.Gln1308Ter)
c.4336C>T (p.Gln1446Ter)
c.3993C>T (p.Pro1331=)
dbSNP
16g.9763364G>CCA394705892GRIN2Ac.4180C>G (p.Gln1394Glu)
c.3366C>G (p.Pro1122=)
n.3430C>G
c.3709C>G (p.Gln1237Glu)
c.*1550C>G (n.*1550C>G)
c.3769C>G (p.Gln1257Glu)
n.3476C>G
c.3426C>G (p.Pro1142=)
c.3837C>G (p.Pro1279=)
c.4021C>G (p.Gln1341Glu)
c.3922C>G (p.Gln1308Glu)
c.4336C>G (p.Gln1446Glu)
c.3993C>G (p.Pro1331=)
dbSNP
16g.9763364G=CA2206692685GRIN2Ac.4180C= (p.Gln1394=)
c.3366C= (p.Pro1122=)
n.3430C=
c.3709C= (p.Gln1237=)
c.*1550C= (n.*1550C=)
c.3769C= (p.Gln1257=)
n.3476C=
c.3426C= (p.Pro1142=)
c.3837C= (p.Pro1279=)
c.4021C= (p.Gln1341=)
c.3922C= (p.Gln1308=)
c.4336C= (p.Gln1446=)
c.3993C= (p.Pro1331=)
16g.9763364G>TCA394705893GRIN2Ac.4180C>A (p.Gln1394Lys)
c.3366C>A (p.Pro1122=)
n.3430C>A
c.3709C>A (p.Gln1237Lys)
c.*1550C>A (n.*1550C>A)
c.3769C>A (p.Gln1257Lys)
n.3476C>A
c.3426C>A (p.Pro1142=)
c.3837C>A (p.Pro1279=)
c.4021C>A (p.Gln1341Lys)
c.3922C>A (p.Gln1308Lys)
c.4336C>A (p.Gln1446Lys)
c.3993C>A (p.Pro1331=)
dbSNP
16g.9763365G>ACA394705896GRIN2Ac.4179C>T (p.Ser1393=)
c.3365C>T (p.Pro1122Leu)
n.3429C>T
c.3708C>T (p.Ser1236=)
c.*1549C>T (n.*1549C>T)
c.3768C>T (p.Ser1256=)
n.3475C>T
c.3425C>T (p.Pro1142Leu)
c.3836C>T (p.Pro1279Leu)
c.4020C>T (p.Ser1340=)
c.3921C>T (p.Ser1307=)
c.4335C>T (p.Ser1445=)
c.3992C>T (p.Pro1331Leu)
dbSNP
16g.9763365G>CCA394705895GRIN2Ac.4179C>G (p.Ser1393=)
c.3365C>G (p.Pro1122Arg)
n.3429C>G
c.3708C>G (p.Ser1236=)
c.*1549C>G (n.*1549C>G)
c.3768C>G (p.Ser1256=)
n.3475C>G
c.3425C>G (p.Pro1142Arg)
c.3836C>G (p.Pro1279Arg)
c.4020C>G (p.Ser1340=)
c.3921C>G (p.Ser1307=)
c.4335C>G (p.Ser1445=)
c.3992C>G (p.Pro1331Arg)
dbSNP
16g.9763365G>TCA394705894GRIN2Ac.4179C>A (p.Ser1393=)
c.3365C>A (p.Pro1122His)
n.3429C>A
c.3708C>A (p.Ser1236=)
c.*1549C>A (n.*1549C>A)
c.3768C>A (p.Ser1256=)
n.3475C>A
c.3425C>A (p.Pro1142His)
c.3836C>A (p.Pro1279His)
c.4020C>A (p.Ser1340=)
c.3921C>A (p.Ser1307=)
c.4335C>A (p.Ser1445=)
c.3992C>A (p.Pro1331His)
dbSNP COSMIC
16g.9763366G>ACA394705897GRIN2Ac.4178C>T (p.Ser1393Phe)
c.3364C>T (p.Pro1122Ser)
n.3428C>T
c.3707C>T (p.Ser1236Phe)
c.*1548C>T (n.*1548C>T)
c.3767C>T (p.Ser1256Phe)
n.3474C>T
c.3424C>T (p.Pro1142Ser)
c.3835C>T (p.Pro1279Ser)
c.4019C>T (p.Ser1340Phe)
c.3920C>T (p.Ser1307Phe)
c.4334C>T (p.Ser1445Phe)
c.3991C>T (p.Pro1331Ser)
dbSNP COSMIC
16g.9763366G>CCA394705898GRIN2Ac.4178C>G (p.Ser1393Cys)
c.3364C>G (p.Pro1122Ala)
n.3428C>G
c.3707C>G (p.Ser1236Cys)
c.*1548C>G (n.*1548C>G)
c.3767C>G (p.Ser1256Cys)
n.3474C>G
c.3424C>G (p.Pro1142Ala)
c.3835C>G (p.Pro1279Ala)
c.4019C>G (p.Ser1340Cys)
c.3920C>G (p.Ser1307Cys)
c.4334C>G (p.Ser1445Cys)
c.3991C>G (p.Pro1331Ala)
dbSNP
16g.9763366G>TCA394705899GRIN2Ac.4178C>A (p.Ser1393Tyr)
c.3364C>A (p.Pro1122Thr)
n.3428C>A
c.3707C>A (p.Ser1236Tyr)
c.*1548C>A (n.*1548C>A)
c.3767C>A (p.Ser1256Tyr)
n.3474C>A
c.3424C>A (p.Pro1142Thr)
c.3835C>A (p.Pro1279Thr)
c.4019C>A (p.Ser1340Tyr)
c.3920C>A (p.Ser1307Tyr)
c.4334C>A (p.Ser1445Tyr)
c.3991C>A (p.Pro1331Thr)
dbSNP
16g.9763367A>CCA394705900GRIN2Ac.4177T>G (p.Ser1393Ala)
c.3363T>G (p.His1121Gln)
n.3427T>G
c.3706T>G (p.Ser1236Ala)
c.*1547T>G (n.*1547T>G)
c.3766T>G (p.Ser1256Ala)
n.3473T>G
c.3423T>G (p.His1141Gln)
c.3834T>G (p.His1278Gln)
c.4018T>G (p.Ser1340Ala)
c.3919T>G (p.Ser1307Ala)
c.4333T>G (p.Ser1445Ala)
c.3990T>G (p.His1330Gln)
16g.9763367A>GCA394705901GRIN2Ac.4177T>C (p.Ser1393Pro)
c.3363T>C (p.His1121=)
n.3427T>C
c.3706T>C (p.Ser1236Pro)
c.*1547T>C (n.*1547T>C)
c.3766T>C (p.Ser1256Pro)
n.3473T>C
c.3423T>C (p.His1141=)
c.3834T>C (p.His1278=)
c.4018T>C (p.Ser1340Pro)
c.3919T>C (p.Ser1307Pro)
c.4333T>C (p.Ser1445Pro)
c.3990T>C (p.His1330=)
dbSNP
16g.9763367A>TCA394705902GRIN2Ac.4177T>A (p.Ser1393Thr)
c.3363T>A (p.His1121Gln)
n.3427T>A
c.3706T>A (p.Ser1236Thr)
c.*1547T>A (n.*1547T>A)
c.3766T>A (p.Ser1256Thr)
n.3473T>A
c.3423T>A (p.His1141Gln)
c.3834T>A (p.His1278Gln)
c.4018T>A (p.Ser1340Thr)
c.3919T>A (p.Ser1307Thr)
c.4333T>A (p.Ser1445Thr)
c.3990T>A (p.His1330Gln)
dbSNP
16g.9763368T>ACA394705903GRIN2Ac.4176A>T (p.Pro1392=)
c.3362A>T (p.His1121Leu)
n.3426A>T
c.3705A>T (p.Pro1235=)
c.*1546A>T (n.*1546A>T)
c.3765A>T (p.Pro1255=)
n.3472A>T
c.3422A>T (p.His1141Leu)
c.3833A>T (p.His1278Leu)
c.4017A>T (p.Pro1339=)
c.3918A>T (p.Pro1306=)
c.4332A>T (p.Pro1444=)
c.3989A>T (p.His1330Leu)
dbSNP
16g.9763368T>CCA10605820GRIN2Ac.4176A>G (p.Pro1392=)
c.3362A>G (p.His1121Arg)
n.3426A>G
c.3705A>G (p.Pro1235=)
c.*1546A>G (n.*1546A>G)
c.3765A>G (p.Pro1255=)
n.3472A>G
c.3422A>G (p.His1141Arg)
c.3833A>G (p.His1278Arg)
c.4017A>G (p.Pro1339=)
c.3918A>G (p.Pro1306=)
c.4332A>G (p.Pro1444=)
c.3989A>G (p.His1330Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.9763368T>GCA394705904GRIN2Ac.4176A>C (p.Pro1392=)
c.3362A>C (p.His1121Pro)
n.3426A>C
c.3705A>C (p.Pro1235=)
c.*1546A>C (n.*1546A>C)
c.3765A>C (p.Pro1255=)
n.3472A>C
c.3422A>C (p.His1141Pro)
c.3833A>C (p.His1278Pro)
c.4017A>C (p.Pro1339=)
c.3918A>C (p.Pro1306=)
c.4332A>C (p.Pro1444=)
c.3989A>C (p.His1330Pro)
gnomAD v4
16g.9763368T=CA2206692686GRIN2Ac.4176A= (p.Pro1392=)
c.3362A= (p.His1121=)
n.3426A=
c.3705A= (p.Pro1235=)
c.*1546A= (n.*1546A=)
c.3765A= (p.Pro1255=)
n.3472A=
c.3422A= (p.His1141=)
c.3833A= (p.His1278=)
c.4017A= (p.Pro1339=)
c.3918A= (p.Pro1306=)
c.4332A= (p.Pro1444=)
c.3989A= (p.His1330=)
16g.9763369G>ACA394705905GRIN2Ac.4175C>T (p.Pro1392Leu)
c.3361C>T (p.His1121Tyr)
n.3425C>T
c.3704C>T (p.Pro1235Leu)
c.*1545C>T (n.*1545C>T)
c.3764C>T (p.Pro1255Leu)
n.3471C>T
c.3421C>T (p.His1141Tyr)
c.3832C>T (p.His1278Tyr)
c.4016C>T (p.Pro1339Leu)
c.3917C>T (p.Pro1306Leu)
c.4331C>T (p.Pro1444Leu)
c.3988C>T (p.His1330Tyr)
dbSNP gnomAD v2 gnomAD v4 COSMIC
16g.9763369G>CCA394705906GRIN2Ac.4175C>G (p.Pro1392Arg)
c.3361C>G (p.His1121Asp)
n.3425C>G
c.3704C>G (p.Pro1235Arg)
c.*1545C>G (n.*1545C>G)
c.3764C>G (p.Pro1255Arg)
n.3471C>G
c.3421C>G (p.His1141Asp)
c.3832C>G (p.His1278Asp)
c.4016C>G (p.Pro1339Arg)
c.3917C>G (p.Pro1306Arg)
c.4331C>G (p.Pro1444Arg)
c.3988C>G (p.His1330Asp)
dbSNP
16g.9763369G=CA2206692687GRIN2Ac.4175C= (p.Pro1392=)
c.3361C= (p.His1121=)
n.3425C=
c.3704C= (p.Pro1235=)
c.*1545C= (n.*1545C=)
c.3764C= (p.Pro1255=)
n.3471C=
c.3421C= (p.His1141=)
c.3832C= (p.His1278=)
c.4016C= (p.Pro1339=)
c.3917C= (p.Pro1306=)
c.4331C= (p.Pro1444=)
c.3988C= (p.His1330=)
16g.9763369G>TCA394705907GRIN2Ac.4175C>A (p.Pro1392Gln)
c.3361C>A (p.His1121Asn)
n.3425C>A
c.3704C>A (p.Pro1235Gln)
c.*1545C>A (n.*1545C>A)
c.3764C>A (p.Pro1255Gln)
n.3471C>A
c.3421C>A (p.His1141Asn)
c.3832C>A (p.His1278Asn)
c.4016C>A (p.Pro1339Gln)
c.3917C>A (p.Pro1306Gln)
c.4331C>A (p.Pro1444Gln)
c.3988C>A (p.His1330Asn)
16g.9763370G>ACA394705910GRIN2Ac.4174C>T (p.Pro1392Ser)
c.3360C>T (p.Cys1120=)
n.3424C>T
c.3703C>T (p.Pro1235Ser)
c.*1544C>T (n.*1544C>T)
c.3763C>T (p.Pro1255Ser)
n.3470C>T
c.3420C>T (p.Cys1140=)
c.3831C>T (p.Cys1277=)
c.4015C>T (p.Pro1339Ser)
c.3916C>T (p.Pro1306Ser)
c.4330C>T (p.Pro1444Ser)
c.3987C>T (p.Cys1329=)
dbSNP gnomAD v4
16g.9763370G>CCA394705909GRIN2Ac.4174C>G (p.Pro1392Ala)
c.3360C>G (p.Cys1120Trp)
n.3424C>G
c.3703C>G (p.Pro1235Ala)
c.*1544C>G (n.*1544C>G)
c.3763C>G (p.Pro1255Ala)
n.3470C>G
c.3420C>G (p.Cys1140Trp)
c.3831C>G (p.Cys1277Trp)
c.4015C>G (p.Pro1339Ala)
c.3916C>G (p.Pro1306Ala)
c.4330C>G (p.Pro1444Ala)
c.3987C>G (p.Cys1329Trp)
dbSNP
16g.9763370G>TCA394705908GRIN2Ac.4174C>A (p.Pro1392Thr)
c.3360C>A (p.Cys1120Ter)
n.3424C>A
c.3703C>A (p.Pro1235Thr)
c.*1544C>A (n.*1544C>A)
c.3763C>A (p.Pro1255Thr)
n.3470C>A
c.3420C>A (p.Cys1140Ter)
c.3831C>A (p.Cys1277Ter)
c.4015C>A (p.Pro1339Thr)
c.3916C>A (p.Pro1306Thr)
c.4330C>A (p.Pro1444Thr)
c.3987C>A (p.Cys1329Ter)
dbSNP
16g.9763371C>ACA394705911GRIN2Ac.4173G>T (p.Leu1391Phe)
c.3359G>T (p.Cys1120Phe)
n.3423G>T
c.3702G>T (p.Leu1234Phe)
c.*1543G>T (n.*1543G>T)
c.3762G>T (p.Leu1254Phe)
n.3469G>T
c.3419G>T (p.Cys1140Phe)
c.3830G>T (p.Cys1277Phe)
c.4014G>T (p.Leu1338Phe)
c.3915G>T (p.Leu1305Phe)
c.4329G>T (p.Leu1443Phe)
c.3986G>T (p.Cys1329Phe)
dbSNP
16g.9763371C>GCA394705912GRIN2Ac.4173G>C (p.Leu1391Phe)
c.3359G>C (p.Cys1120Ser)
n.3423G>C
c.3702G>C (p.Leu1234Phe)
c.*1543G>C (n.*1543G>C)
c.3762G>C (p.Leu1254Phe)
n.3469G>C
c.3419G>C (p.Cys1140Ser)
c.3830G>C (p.Cys1277Ser)
c.4014G>C (p.Leu1338Phe)
c.3915G>C (p.Leu1305Phe)
c.4329G>C (p.Leu1443Phe)
c.3986G>C (p.Cys1329Ser)
dbSNP gnomAD v4
16g.9763371C>TCA394705913GRIN2Ac.4173G>A (p.Leu1391=)
c.3359G>A (p.Cys1120Tyr)
n.3423G>A
c.3702G>A (p.Leu1234=)
c.*1543G>A (n.*1543G>A)
c.3762G>A (p.Leu1254=)
n.3469G>A
c.3419G>A (p.Cys1140Tyr)
c.3830G>A (p.Cys1277Tyr)
c.4014G>A (p.Leu1338=)
c.3915G>A (p.Leu1305=)
c.4329G>A (p.Leu1443=)
c.3986G>A (p.Cys1329Tyr)
dbSNP
16g.9763372A=CA2206692688GRIN2Ac.4172T= (p.Leu1391=)
c.3358T= (p.Cys1120=)
n.3422T=
c.3701T= (p.Leu1234=)
c.*1542T= (n.*1542T=)
c.3761T= (p.Leu1254=)
n.3468T=
c.3418T= (p.Cys1140=)
c.3829T= (p.Cys1277=)
c.4013T= (p.Leu1338=)
c.3914T= (p.Leu1305=)
c.4328T= (p.Leu1443=)
c.3985T= (p.Cys1329=)
16g.9763372A>CCA394705914GRIN2Ac.4172T>G (p.Leu1391Trp)
c.3358T>G (p.Cys1120Gly)
n.3422T>G
c.3701T>G (p.Leu1234Trp)
c.*1542T>G (n.*1542T>G)
c.3761T>G (p.Leu1254Trp)
n.3468T>G
c.3418T>G (p.Cys1140Gly)
c.3829T>G (p.Cys1277Gly)
c.4013T>G (p.Leu1338Trp)
c.3914T>G (p.Leu1305Trp)
c.4328T>G (p.Leu1443Trp)
c.3985T>G (p.Cys1329Gly)
16g.9763372A>GCA394705915GRIN2Ac.4172T>C (p.Leu1391Ser)
c.3358T>C (p.Cys1120Arg)
n.3422T>C
c.3701T>C (p.Leu1234Ser)
c.*1542T>C (n.*1542T>C)
c.3761T>C (p.Leu1254Ser)
n.3468T>C
c.3418T>C (p.Cys1140Arg)
c.3829T>C (p.Cys1277Arg)
c.4013T>C (p.Leu1338Ser)
c.3914T>C (p.Leu1305Ser)
c.4328T>C (p.Leu1443Ser)
c.3985T>C (p.Cys1329Arg)
16g.9763372A>TCA394705916GRIN2Ac.4172T>A (p.Leu1391Ter)
c.3358T>A (p.Cys1120Ser)
n.3422T>A
c.3701T>A (p.Leu1234Ter)
c.*1542T>A (n.*1542T>A)
c.3761T>A (p.Leu1254Ter)
n.3468T>A
c.3418T>A (p.Cys1140Ser)
c.3829T>A (p.Cys1277Ser)
c.4013T>A (p.Leu1338Ter)
c.3914T>A (p.Leu1305Ter)
c.4328T>A (p.Leu1443Ter)
c.3985T>A (p.Cys1329Ser)
dbSNP
16g.9763373A>CCA394705918GRIN2Ac.4171T>G (p.Leu1391Val)
c.3357T>G (p.Arg1119=)
n.3421T>G
c.3700T>G (p.Leu1234Val)
c.*1541T>G (n.*1541T>G)
c.3760T>G (p.Leu1254Val)
n.3467T>G
c.3417T>G (p.Arg1139=)
c.3828T>G (p.Arg1276=)
c.4012T>G (p.Leu1338Val)
c.3913T>G (p.Leu1305Val)
c.4327T>G (p.Leu1443Val)
c.3984T>G (p.Arg1328=)
dbSNP COSMIC
16g.9763373A>GCA493692531GRIN2Ac.4171T>C (p.Leu1391=)
c.3357T>C (p.Arg1119=)
n.3421T>C
c.3700T>C (p.Leu1234=)
c.*1541T>C (n.*1541T>C)
c.3760T>C (p.Leu1254=)
n.3467T>C
c.3417T>C (p.Arg1139=)
c.3828T>C (p.Arg1276=)
c.4012T>C (p.Leu1338=)
c.3913T>C (p.Leu1305=)
c.4327T>C (p.Leu1443=)
c.3984T>C (p.Arg1328=)
dbSNP
16g.9763373A>TCA394705917GRIN2Ac.4171T>A (p.Leu1391Met)
c.3357T>A (p.Arg1119=)
n.3421T>A
c.3700T>A (p.Leu1234Met)
c.*1541T>A (n.*1541T>A)
c.3760T>A (p.Leu1254Met)
n.3467T>A
c.3417T>A (p.Arg1139=)
c.3828T>A (p.Arg1276=)
c.4012T>A (p.Leu1338Met)
c.3913T>A (p.Leu1305Met)
c.4327T>A (p.Leu1443Met)
c.3984T>A (p.Arg1328=)
dbSNP
16g.9763374C>ACA394705919GRIN2Ac.4170G>T (p.Ser1390=)
c.3356G>T (p.Arg1119Leu)
n.3420G>T
c.3699G>T (p.Ser1233=)
c.*1540G>T (n.*1540G>T)
c.3759G>T (p.Ser1253=)
n.3466G>T
c.3416G>T (p.Arg1139Leu)
c.3827G>T (p.Arg1276Leu)
c.4011G>T (p.Ser1337=)
c.3912G>T (p.Ser1304=)
c.4326G>T (p.Ser1442=)
c.3983G>T (p.Arg1328Leu)
dbSNP gnomAD v4
16g.9763374C=CA2206692689GRIN2Ac.4170G= (p.Ser1390=)
c.3356G= (p.Arg1119=)
n.3420G=
c.3699G= (p.Ser1233=)
c.*1540G= (n.*1540G=)
c.3759G= (p.Ser1253=)
n.3466G=
c.3416G= (p.Arg1139=)
c.3827G= (p.Arg1276=)
c.4011G= (p.Ser1337=)
c.3912G= (p.Ser1304=)
c.4326G= (p.Ser1442=)
c.3983G= (p.Arg1328=)
16g.9763374C>GCA394705920GRIN2Ac.4170G>C (p.Ser1390=)
c.3356G>C (p.Arg1119Pro)
n.3420G>C
c.3699G>C (p.Ser1233=)
c.*1540G>C (n.*1540G>C)
c.3759G>C (p.Ser1253=)
n.3466G>C
c.3416G>C (p.Arg1139Pro)
c.3827G>C (p.Arg1276Pro)
c.4011G>C (p.Ser1337=)
c.3912G>C (p.Ser1304=)
c.4326G>C (p.Ser1442=)
c.3983G>C (p.Arg1328Pro)
dbSNP
16g.9763374C>TCA16607154GRIN2Ac.4170G>A (p.Ser1390=)
c.3356G>A (p.Arg1119His)
n.3420G>A
c.3699G>A (p.Ser1233=)
c.*1540G>A (n.*1540G>A)
c.3759G>A (p.Ser1253=)
n.3466G>A
c.3416G>A (p.Arg1139His)
c.3827G>A (p.Arg1276His)
c.4011G>A (p.Ser1337=)
c.3912G>A (p.Ser1304=)
c.4326G>A (p.Ser1442=)
c.3983G>A (p.Arg1328His)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.9763375G>ACA277536018GRIN2Ac.4169C>T (p.Ser1390Leu)
c.3355C>T (p.Arg1119Cys)
n.3419C>T
c.3698C>T (p.Ser1233Leu)
c.*1539C>T (n.*1539C>T)
c.3758C>T (p.Ser1253Leu)
n.3465C>T
c.3415C>T (p.Arg1139Cys)
c.3826C>T (p.Arg1276Cys)
c.4010C>T (p.Ser1337Leu)
c.3911C>T (p.Ser1304Leu)
c.4325C>T (p.Ser1442Leu)
c.3982C>T (p.Arg1328Cys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.9763375G>CCA7896203GRIN2Ac.4169C>G (p.Ser1390Trp)
c.3355C>G (p.Arg1119Gly)
n.3419C>G
c.3698C>G (p.Ser1233Trp)
c.*1539C>G (n.*1539C>G)
c.3758C>G (p.Ser1253Trp)
n.3465C>G
c.3415C>G (p.Arg1139Gly)
c.3826C>G (p.Arg1276Gly)
c.4010C>G (p.Ser1337Trp)
c.3911C>G (p.Ser1304Trp)
c.4325C>G (p.Ser1442Trp)
c.3982C>G (p.Arg1328Gly)
dbSNP ExAC gnomAD v2 gnomAD v4
16g.9763375G=CA2206692690GRIN2Ac.4169C= (p.Ser1390=)
c.3355C= (p.Arg1119=)
n.3419C=
c.3698C= (p.Ser1233=)
c.*1539C= (n.*1539C=)
c.3758C= (p.Ser1253=)
n.3465C=
c.3415C= (p.Arg1139=)
c.3826C= (p.Arg1276=)
c.4010C= (p.Ser1337=)
c.3911C= (p.Ser1304=)
c.4325C= (p.Ser1442=)
c.3982C= (p.Arg1328=)
16g.9763375G>TCA394705921GRIN2Ac.4169C>A (p.Ser1390Ter)
c.3355C>A (p.Arg1119Ser)
n.3419C>A
c.3698C>A (p.Ser1233Ter)
c.*1539C>A (n.*1539C>A)
c.3758C>A (p.Ser1253Ter)
n.3465C>A
c.3415C>A (p.Arg1139Ser)
c.3826C>A (p.Arg1276Ser)
c.4010C>A (p.Ser1337Ter)
c.3911C>A (p.Ser1304Ter)
c.4325C>A (p.Ser1442Ter)
c.3982C>A (p.Arg1328Ser)
dbSNP
16g.9763376A=CA2206692691GRIN2Ac.4168T= (p.Ser1390=)
c.3354T= (p.Thr1118=)
n.3418T=
c.3697T= (p.Ser1233=)
c.*1538T= (n.*1538T=)
c.3757T= (p.Ser1253=)
n.3464T=
c.3414T= (p.Thr1138=)
c.3825T= (p.Thr1275=)
c.4009T= (p.Ser1337=)
c.3910T= (p.Ser1304=)
c.4324T= (p.Ser1442=)
c.3981T= (p.Thr1327=)
16g.9763376A>CCA394705922GRIN2Ac.4168T>G (p.Ser1390Ala)
c.3354T>G (p.Thr1118=)
n.3418T>G
c.3697T>G (p.Ser1233Ala)
c.*1538T>G (n.*1538T>G)
c.3757T>G (p.Ser1253Ala)
n.3464T>G
c.3414T>G (p.Thr1138=)
c.3825T>G (p.Thr1275=)
c.4009T>G (p.Ser1337Ala)
c.3910T>G (p.Ser1304Ala)
c.4324T>G (p.Ser1442Ala)
c.3981T>G (p.Thr1327=)
COSMIC
16g.9763376A>GCA394705924GRIN2Ac.4168T>C (p.Ser1390Pro)
c.3354T>C (p.Thr1118=)
n.3418T>C
c.3697T>C (p.Ser1233Pro)
c.*1538T>C (n.*1538T>C)
c.3757T>C (p.Ser1253Pro)
n.3464T>C
c.3414T>C (p.Thr1138=)
c.3825T>C (p.Thr1275=)
c.4009T>C (p.Ser1337Pro)
c.3910T>C (p.Ser1304Pro)
c.4324T>C (p.Ser1442Pro)
c.3981T>C (p.Thr1327=)
dbSNP gnomAD v3 gnomAD v4
16g.9763376A>TCA394705923GRIN2Ac.4168T>A (p.Ser1390Thr)
c.3354T>A (p.Thr1118=)
n.3418T>A
c.3697T>A (p.Ser1233Thr)
c.*1538T>A (n.*1538T>A)
c.3757T>A (p.Ser1253Thr)
n.3464T>A
c.3414T>A (p.Thr1138=)
c.3825T>A (p.Thr1275=)
c.4009T>A (p.Ser1337Thr)
c.3910T>A (p.Ser1304Thr)
c.4324T>A (p.Ser1442Thr)
c.3981T>A (p.Thr1327=)
dbSNP
16g.9763377G>ACA7896204GRIN2Ac.4167C>T (p.His1389=)
c.3353C>T (p.Thr1118Ile)
n.3417C>T
c.3696C>T (p.His1232=)
c.*1537C>T (n.*1537C>T)
c.3756C>T (p.His1252=)
n.3463C>T
c.3413C>T (p.Thr1138Ile)
c.3824C>T (p.Thr1275Ile)
c.4008C>T (p.His1336=)
c.3909C>T (p.His1303=)
c.4323C>T (p.His1441=)
c.3980C>T (p.Thr1327Ile)
dbSNP ExAC gnomAD v2 gnomAD v4
16g.9763377G>CCA394705925GRIN2Ac.4167C>G (p.His1389Gln)
c.3353C>G (p.Thr1118Ser)
n.3417C>G
c.3696C>G (p.His1232Gln)
c.*1537C>G (n.*1537C>G)
c.3756C>G (p.His1252Gln)
n.3463C>G
c.3413C>G (p.Thr1138Ser)
c.3824C>G (p.Thr1275Ser)
c.4008C>G (p.His1336Gln)
c.3909C>G (p.His1303Gln)
c.4323C>G (p.His1441Gln)
c.3980C>G (p.Thr1327Ser)
ClinVar dbSNP gnomAD v4
16g.9763377G=CA2206692692GRIN2Ac.4167C= (p.His1389=)
c.3353C= (p.Thr1118=)
n.3417C=
c.3696C= (p.His1232=)
c.*1537C= (n.*1537C=)
c.3756C= (p.His1252=)
n.3463C=
c.3413C= (p.Thr1138=)
c.3824C= (p.Thr1275=)
c.4008C= (p.His1336=)
c.3909C= (p.His1303=)
c.4323C= (p.His1441=)
c.3980C= (p.Thr1327=)
16g.9763377G>TCA394705926GRIN2Ac.4167C>A (p.His1389Gln)
c.3353C>A (p.Thr1118Asn)
n.3417C>A
c.3696C>A (p.His1232Gln)
c.*1537C>A (n.*1537C>A)
c.3756C>A (p.His1252Gln)
n.3463C>A
c.3413C>A (p.Thr1138Asn)
c.3824C>A (p.Thr1275Asn)
c.4008C>A (p.His1336Gln)
c.3909C>A (p.His1303Gln)
c.4323C>A (p.His1441Gln)
c.3980C>A (p.Thr1327Asn)
dbSNP
16g.9763378T>ACA394705927GRIN2Ac.4166A>T (p.His1389Leu)
c.3352A>T (p.Thr1118Ser)
n.3416A>T
c.3695A>T (p.His1232Leu)
c.*1536A>T (n.*1536A>T)
c.3755A>T (p.His1252Leu)
n.3462A>T
c.3412A>T (p.Thr1138Ser)
c.3823A>T (p.Thr1275Ser)
c.4007A>T (p.His1336Leu)
c.3908A>T (p.His1303Leu)
c.4322A>T (p.His1441Leu)
c.3979A>T (p.Thr1327Ser)
dbSNP
16g.9763378T>CCA394705928GRIN2Ac.4166A>G (p.His1389Arg)
c.3352A>G (p.Thr1118Ala)
n.3416A>G
c.3695A>G (p.His1232Arg)
c.*1536A>G (n.*1536A>G)
c.3755A>G (p.His1252Arg)
n.3462A>G
c.3412A>G (p.Thr1138Ala)
c.3823A>G (p.Thr1275Ala)
c.4007A>G (p.His1336Arg)
c.3908A>G (p.His1303Arg)
c.4322A>G (p.His1441Arg)
c.3979A>G (p.Thr1327Ala)
gnomAD v4
16g.9763378T>GCA394705929GRIN2Ac.4166A>C (p.His1389Pro)
c.3352A>C (p.Thr1118Pro)
n.3416A>C
c.3695A>C (p.His1232Pro)
c.*1536A>C (n.*1536A>C)
c.3755A>C (p.His1252Pro)
n.3462A>C
c.3412A>C (p.Thr1138Pro)
c.3823A>C (p.Thr1275Pro)
c.4007A>C (p.His1336Pro)
c.3908A>C (p.His1303Pro)
c.4322A>C (p.His1441Pro)
c.3979A>C (p.Thr1327Pro)
dbSNP
16g.9763378dupCA2631674848GRIN2Ac.4166dup (p.His1389GlnfsTer10)
c.3352dup (p.Thr1118AsnfsTer?)
n.3416dup
c.3695dup (p.His1232GlnfsTer10)
c.*1536dup (n.*1536dup)
c.3755dup (p.His1252GlnfsTer10)
n.3462dup
c.3412dup (p.Thr1138AsnfsTer?)
c.3823dup (p.Thr1275AsnfsTer?)
c.4007dup (p.His1336GlnfsTer10)
c.3908dup (p.His1303GlnfsTer10)
c.4322dup (p.His1441GlnfsTer10)
c.3979dup (p.Thr1327AsnfsTer?)
gnomAD v4
16g.9763379G>ACA394705930GRIN2Ac.4165C>T (p.His1389Tyr)
c.3351C>T (p.Asn1117=)
n.3415C>T
c.3694C>T (p.His1232Tyr)
c.*1535C>T (n.*1535C>T)
c.3754C>T (p.His1252Tyr)
n.3461C>T
c.3411C>T (p.Asn1137=)
c.3822C>T (p.Asn1274=)
c.4006C>T (p.His1336Tyr)
c.3907C>T (p.His1303Tyr)
c.4321C>T (p.His1441Tyr)
c.3978C>T (p.Asn1326=)
ClinVar dbSNP
16g.9763379G>CCA394705931GRIN2Ac.4165C>G (p.His1389Asp)
c.3351C>G (p.Asn1117Lys)
n.3415C>G
c.3694C>G (p.His1232Asp)
c.*1535C>G (n.*1535C>G)
c.3754C>G (p.His1252Asp)
n.3461C>G
c.3411C>G (p.Asn1137Lys)
c.3822C>G (p.Asn1274Lys)
c.4006C>G (p.His1336Asp)
c.3907C>G (p.His1303Asp)
c.4321C>G (p.His1441Asp)
c.3978C>G (p.Asn1326Lys)
dbSNP
16g.9763379G>TCA394705932GRIN2Ac.4165C>A (p.His1389Asn)
c.3351C>A (p.Asn1117Lys)
n.3415C>A
c.3694C>A (p.His1232Asn)
c.*1535C>A (n.*1535C>A)
c.3754C>A (p.His1252Asn)
n.3461C>A
c.3411C>A (p.Asn1137Lys)
c.3822C>A (p.Asn1274Lys)
c.4006C>A (p.His1336Asn)
c.3907C>A (p.His1303Asn)
c.4321C>A (p.His1441Asn)
c.3978C>A (p.Asn1326Lys)
dbSNP
16g.9763380T>ACA394705933GRIN2Ac.4164A>T (p.Lys1388Asn)
c.3350A>T (p.Asn1117Ile)
n.3414A>T
c.3693A>T (p.Lys1231Asn)
c.*1534A>T (n.*1534A>T)
c.3753A>T (p.Lys1251Asn)
n.3460A>T
c.3410A>T (p.Asn1137Ile)
c.3821A>T (p.Asn1274Ile)
c.4005A>T (p.Lys1335Asn)
c.3906A>T (p.Lys1302Asn)
c.4320A>T (p.Lys1440Asn)
c.3977A>T (p.Asn1326Ile)
dbSNP
16g.9763380T>CCA394705934GRIN2Ac.4164A>G (p.Lys1388=)
c.3350A>G (p.Asn1117Ser)
n.3414A>G
c.3693A>G (p.Lys1231=)
c.*1534A>G (n.*1534A>G)
c.3753A>G (p.Lys1251=)
n.3460A>G
c.3410A>G (p.Asn1137Ser)
c.3821A>G (p.Asn1274Ser)
c.4005A>G (p.Lys1335=)
c.3906A>G (p.Lys1302=)
c.4320A>G (p.Lys1440=)
c.3977A>G (p.Asn1326Ser)
ClinVar dbSNP gnomAD v4
16g.9763380T>GCA394705935GRIN2Ac.4164A>C (p.Lys1388Asn)
c.3350A>C (p.Asn1117Thr)
n.3414A>C
c.3693A>C (p.Lys1231Asn)
c.*1534A>C (n.*1534A>C)
c.3753A>C (p.Lys1251Asn)
n.3460A>C
c.3410A>C (p.Asn1137Thr)
c.3821A>C (p.Asn1274Thr)
c.4005A>C (p.Lys1335Asn)
c.3906A>C (p.Lys1302Asn)
c.4320A>C (p.Lys1440Asn)
c.3977A>C (p.Asn1326Thr)
dbSNP
16g.9763381T>ACA394705937GRIN2Ac.4163A>T (p.Lys1388Ile)
c.3349A>T (p.Asn1117Tyr)
n.3413A>T
c.3692A>T (p.Lys1231Ile)
c.*1533A>T (n.*1533A>T)
c.3752A>T (p.Lys1251Ile)
n.3459A>T
c.3409A>T (p.Asn1137Tyr)
c.3820A>T (p.Asn1274Tyr)
c.4004A>T (p.Lys1335Ile)
c.3905A>T (p.Lys1302Ile)
c.4319A>T (p.Lys1440Ile)
c.3976A>T (p.Asn1326Tyr)
dbSNP
16g.9763381T>CCA394705938GRIN2Ac.4163A>G (p.Lys1388Arg)
c.3349A>G (p.Asn1117Asp)
n.3413A>G
c.3692A>G (p.Lys1231Arg)
c.*1533A>G (n.*1533A>G)
c.3752A>G (p.Lys1251Arg)
n.3459A>G
c.3409A>G (p.Asn1137Asp)
c.3820A>G (p.Asn1274Asp)
c.4004A>G (p.Lys1335Arg)
c.3905A>G (p.Lys1302Arg)
c.4319A>G (p.Lys1440Arg)
c.3976A>G (p.Asn1326Asp)
dbSNP
16g.9763381T>GCA394705936GRIN2Ac.4163A>C (p.Lys1388Thr)
c.3349A>C (p.Asn1117His)
n.3413A>C
c.3692A>C (p.Lys1231Thr)
c.*1533A>C (n.*1533A>C)
c.3752A>C (p.Lys1251Thr)
n.3459A>C
c.3409A>C (p.Asn1137His)
c.3820A>C (p.Asn1274His)
c.4004A>C (p.Lys1335Thr)
c.3905A>C (p.Lys1302Thr)
c.4319A>C (p.Lys1440Thr)
c.3976A>C (p.Asn1326His)
dbSNP
16g.9763382T>ACA394705939GRIN2Ac.4162A>T (p.Lys1388Ter)
c.3348A>T (p.Thr1116=)
n.3412A>T
c.3691A>T (p.Lys1231Ter)
c.*1532A>T (n.*1532A>T)
c.3751A>T (p.Lys1251Ter)
n.3458A>T
c.3408A>T (p.Thr1136=)
c.3819A>T (p.Thr1273=)
c.4003A>T (p.Lys1335Ter)
c.3904A>T (p.Lys1302Ter)
c.4318A>T (p.Lys1440Ter)
c.3975A>T (p.Thr1325=)
dbSNP
16g.9763382T>CCA394705941GRIN2Ac.4162A>G (p.Lys1388Glu)
c.3348A>G (p.Thr1116=)
n.3412A>G
c.3691A>G (p.Lys1231Glu)
c.*1532A>G (n.*1532A>G)
c.3751A>G (p.Lys1251Glu)
n.3458A>G
c.3408A>G (p.Thr1136=)
c.3819A>G (p.Thr1273=)
c.4003A>G (p.Lys1335Glu)
c.3904A>G (p.Lys1302Glu)
c.4318A>G (p.Lys1440Glu)
c.3975A>G (p.Thr1325=)
dbSNP gnomAD v4
16g.9763382T>GCA394705940GRIN2Ac.4162A>C (p.Lys1388Gln)
c.3348A>C (p.Thr1116=)
n.3412A>C
c.3691A>C (p.Lys1231Gln)
c.*1532A>C (n.*1532A>C)
c.3751A>C (p.Lys1251Gln)
n.3458A>C
c.3408A>C (p.Thr1136=)
c.3819A>C (p.Thr1273=)
c.4003A>C (p.Lys1335Gln)
c.3904A>C (p.Lys1302Gln)
c.4318A>C (p.Lys1440Gln)
c.3975A>C (p.Thr1325=)
dbSNP gnomAD v2 gnomAD v4
16g.9763382T=CA2206692693GRIN2Ac.4162A= (p.Lys1388=)
c.3348A= (p.Thr1116=)
n.3412A=
c.3691A= (p.Lys1231=)
c.*1532A= (n.*1532A=)
c.3751A= (p.Lys1251=)
n.3458A=
c.3408A= (p.Thr1136=)
c.3819A= (p.Thr1273=)
c.4003A= (p.Lys1335=)
c.3904A= (p.Lys1302=)
c.4318A= (p.Lys1440=)
c.3975A= (p.Thr1325=)
16g.9763383G>ACA394705942GRIN2Ac.4161C>T (p.Tyr1387=)
c.3347C>T (p.Thr1116Ile)
n.3411C>T
c.3690C>T (p.Tyr1230=)
c.*1531C>T (n.*1531C>T)
c.3750C>T (p.Tyr1250=)
n.3457C>T
c.3407C>T (p.Thr1136Ile)
c.3818C>T (p.Thr1273Ile)
c.4002C>T (p.Tyr1334=)
c.3903C>T (p.Tyr1301=)
c.4317C>T (p.Tyr1439=)
c.3974C>T (p.Thr1325Ile)
dbSNP
16g.9763383G>CCA394705944GRIN2Ac.4161C>G (p.Tyr1387Ter)
c.3347C>G (p.Thr1116Arg)
n.3411C>G
c.3690C>G (p.Tyr1230Ter)
c.*1531C>G (n.*1531C>G)
c.3750C>G (p.Tyr1250Ter)
n.3457C>G
c.3407C>G (p.Thr1136Arg)
c.3818C>G (p.Thr1273Arg)
c.4002C>G (p.Tyr1334Ter)
c.3903C>G (p.Tyr1301Ter)
c.4317C>G (p.Tyr1439Ter)
c.3974C>G (p.Thr1325Arg)
dbSNP
16g.9763383G>TCA394705943GRIN2Ac.4161C>A (p.Tyr1387Ter)
c.3347C>A (p.Thr1116Lys)
n.3411C>A
c.3690C>A (p.Tyr1230Ter)
c.*1531C>A (n.*1531C>A)
c.3750C>A (p.Tyr1250Ter)
n.3457C>A
c.3407C>A (p.Thr1136Lys)
c.3818C>A (p.Thr1273Lys)
c.4002C>A (p.Tyr1334Ter)
c.3903C>A (p.Tyr1301Ter)
c.4317C>A (p.Tyr1439Ter)
c.3974C>A (p.Thr1325Lys)
dbSNP COSMIC
16g.9763384T>ACA394705945GRIN2Ac.4160A>T (p.Tyr1387Phe)
c.3346A>T (p.Thr1116Ser)
n.3410A>T
c.3689A>T (p.Tyr1230Phe)
c.*1530A>T (n.*1530A>T)
c.3749A>T (p.Tyr1250Phe)
n.3456A>T
c.3406A>T (p.Thr1136Ser)
c.3817A>T (p.Thr1273Ser)
c.4001A>T (p.Tyr1334Phe)
c.3902A>T (p.Tyr1301Phe)
c.4316A>T (p.Tyr1439Phe)
c.3973A>T (p.Thr1325Ser)
16g.9763384T>CCA394705946GRIN2Ac.4160A>G (p.Tyr1387Cys)
c.3346A>G (p.Thr1116Ala)
n.3410A>G
c.3689A>G (p.Tyr1230Cys)
c.*1530A>G (n.*1530A>G)
c.3749A>G (p.Tyr1250Cys)
n.3456A>G
c.3406A>G (p.Thr1136Ala)
c.3817A>G (p.Thr1273Ala)
c.4001A>G (p.Tyr1334Cys)
c.3902A>G (p.Tyr1301Cys)
c.4316A>G (p.Tyr1439Cys)
c.3973A>G (p.Thr1325Ala)
16g.9763384T>GCA394705947GRIN2Ac.4160A>C (p.Tyr1387Ser)
c.3346A>C (p.Thr1116Pro)
n.3410A>C
c.3689A>C (p.Tyr1230Ser)
c.*1530A>C (n.*1530A>C)
c.3749A>C (p.Tyr1250Ser)
n.3456A>C
c.3406A>C (p.Thr1136Pro)
c.3817A>C (p.Thr1273Pro)
c.4001A>C (p.Tyr1334Ser)
c.3902A>C (p.Tyr1301Ser)
c.4316A>C (p.Tyr1439Ser)
c.3973A>C (p.Thr1325Pro)
16g.9763385A=CA2206692694GRIN2Ac.4159T= (p.Tyr1387=)
c.3345T= (p.Leu1115=)
n.3409T=
c.3688T= (p.Tyr1230=)
c.*1529T= (n.*1529T=)
c.3748T= (p.Tyr1250=)
n.3455T=
c.3405T= (p.Leu1135=)
c.3816T= (p.Leu1272=)
c.4000T= (p.Tyr1334=)
c.3901T= (p.Tyr1301=)
c.4315T= (p.Tyr1439=)
c.3972T= (p.Leu1324=)
16g.9763385A>CCA394705948GRIN2Ac.4159T>G (p.Tyr1387Asp)
c.3345T>G (p.Leu1115=)
n.3409T>G
c.3688T>G (p.Tyr1230Asp)
c.*1529T>G (n.*1529T>G)
c.3748T>G (p.Tyr1250Asp)
n.3455T>G
c.3405T>G (p.Leu1135=)
c.3816T>G (p.Leu1272=)
c.4000T>G (p.Tyr1334Asp)
c.3901T>G (p.Tyr1301Asp)
c.4315T>G (p.Tyr1439Asp)
c.3972T>G (p.Leu1324=)
16g.9763385A>GCA394705949GRIN2Ac.4159T>C (p.Tyr1387His)
c.3345T>C (p.Leu1115=)
n.3409T>C
c.3688T>C (p.Tyr1230His)
c.*1529T>C (n.*1529T>C)
c.3748T>C (p.Tyr1250His)
n.3455T>C
c.3405T>C (p.Leu1135=)
c.3816T>C (p.Leu1272=)
c.4000T>C (p.Tyr1334His)
c.3901T>C (p.Tyr1301His)
c.4315T>C (p.Tyr1439His)
c.3972T>C (p.Leu1324=)
16g.9763385A>TCA277536051GRIN2Ac.4159T>A (p.Tyr1387Asn)
c.3345T>A (p.Leu1115=)
n.3409T>A
c.3688T>A (p.Tyr1230Asn)
c.*1529T>A (n.*1529T>A)
c.3748T>A (p.Tyr1250Asn)
n.3455T>A
c.3405T>A (p.Leu1135=)
c.3816T>A (p.Leu1272=)
c.4000T>A (p.Tyr1334Asn)
c.3901T>A (p.Tyr1301Asn)
c.4315T>A (p.Tyr1439Asn)
c.3972T>A (p.Leu1324=)
dbSNP gnomAD v4
16g.9763386A>CCA394705950GRIN2Ac.4158T>G (p.Pro1386=)
c.3344T>G (p.Leu1115Arg)
n.3408T>G
c.3687T>G (p.Pro1229=)
c.*1528T>G (n.*1528T>G)
c.3747T>G (p.Pro1249=)
n.3454T>G
c.3404T>G (p.Leu1135Arg)
c.3815T>G (p.Leu1272Arg)
c.3999T>G (p.Pro1333=)
c.3900T>G (p.Pro1300=)
c.4314T>G (p.Pro1438=)
c.3971T>G (p.Leu1324Arg)
16g.9763386A>GCA394705951GRIN2Ac.4158T>C (p.Pro1386=)
c.3344T>C (p.Leu1115Pro)
n.3408T>C
c.3687T>C (p.Pro1229=)
c.*1528T>C (n.*1528T>C)
c.3747T>C (p.Pro1249=)
n.3454T>C
c.3404T>C (p.Leu1135Pro)
c.3815T>C (p.Leu1272Pro)
c.3999T>C (p.Pro1333=)
c.3900T>C (p.Pro1300=)
c.4314T>C (p.Pro1438=)
c.3971T>C (p.Leu1324Pro)
dbSNP
16g.9763386A>TCA394705952GRIN2Ac.4158T>A (p.Pro1386=)
c.3344T>A (p.Leu1115His)
n.3408T>A
c.3687T>A (p.Pro1229=)
c.*1528T>A (n.*1528T>A)
c.3747T>A (p.Pro1249=)
n.3454T>A
c.3404T>A (p.Leu1135His)
c.3815T>A (p.Leu1272His)
c.3999T>A (p.Pro1333=)
c.3900T>A (p.Pro1300=)
c.4314T>A (p.Pro1438=)
c.3971T>A (p.Leu1324His)
dbSNP
16g.9763387G>ACA394705953GRIN2Ac.4157C>T (p.Pro1386Leu)
c.3343C>T (p.Leu1115Phe)
n.3407C>T
c.3686C>T (p.Pro1229Leu)
c.*1527C>T (n.*1527C>T)
c.3746C>T (p.Pro1249Leu)
n.3453C>T
c.3403C>T (p.Leu1135Phe)
c.3814C>T (p.Leu1272Phe)
c.3998C>T (p.Pro1333Leu)
c.3899C>T (p.Pro1300Leu)
c.4313C>T (p.Pro1438Leu)
c.3970C>T (p.Leu1324Phe)
ClinVar dbSNP gnomAD v4
16g.9763387G>CCA394705954GRIN2Ac.4157C>G (p.Pro1386Arg)
c.3343C>G (p.Leu1115Val)
n.3407C>G
c.3686C>G (p.Pro1229Arg)
c.*1527C>G (n.*1527C>G)
c.3746C>G (p.Pro1249Arg)
n.3453C>G
c.3403C>G (p.Leu1135Val)
c.3814C>G (p.Leu1272Val)
c.3998C>G (p.Pro1333Arg)
c.3899C>G (p.Pro1300Arg)
c.4313C>G (p.Pro1438Arg)
c.3970C>G (p.Leu1324Val)
gnomAD v4
16g.9763387G=CA2206692695GRIN2Ac.4157C= (p.Pro1386=)
c.3343C= (p.Leu1115=)
n.3407C=
c.3686C= (p.Pro1229=)
c.*1527C= (n.*1527C=)
c.3746C= (p.Pro1249=)
n.3453C=
c.3403C= (p.Leu1135=)
c.3814C= (p.Leu1272=)
c.3998C= (p.Pro1333=)
c.3899C= (p.Pro1300=)
c.4313C= (p.Pro1438=)
c.3970C= (p.Leu1324=)
16g.9763387G>TCA394705955GRIN2Ac.4157C>A (p.Pro1386His)
c.3343C>A (p.Leu1115Ile)
n.3407C>A
c.3686C>A (p.Pro1229His)
c.*1527C>A (n.*1527C>A)
c.3746C>A (p.Pro1249His)
n.3453C>A
c.3403C>A (p.Leu1135Ile)
c.3814C>A (p.Leu1272Ile)
c.3998C>A (p.Pro1333His)
c.3899C>A (p.Pro1300His)
c.4313C>A (p.Pro1438His)
c.3970C>A (p.Leu1324Ile)
dbSNP
16g.9763388G>ACA394705956GRIN2Ac.4156C>T (p.Pro1386Ser)
c.3342C>T (p.Thr1114=)
n.3406C>T
c.3685C>T (p.Pro1229Ser)
c.*1526C>T (n.*1526C>T)
c.3745C>T (p.Pro1249Ser)
n.3452C>T
c.3402C>T (p.Thr1134=)
c.3813C>T (p.Thr1271=)
c.3997C>T (p.Pro1333Ser)
c.3898C>T (p.Pro1300Ser)
c.4312C>T (p.Pro1438Ser)
c.3969C>T (p.Thr1323=)
dbSNP gnomAD v4
16g.9763388G>CCA394705958GRIN2Ac.4156C>G (p.Pro1386Ala)
c.3342C>G (p.Thr1114=)
n.3406C>G
c.3685C>G (p.Pro1229Ala)
c.*1526C>G (n.*1526C>G)
c.3745C>G (p.Pro1249Ala)
n.3452C>G
c.3402C>G (p.Thr1134=)
c.3813C>G (p.Thr1271=)
c.3997C>G (p.Pro1333Ala)
c.3898C>G (p.Pro1300Ala)
c.4312C>G (p.Pro1438Ala)
c.3969C>G (p.Thr1323=)
dbSNP
16g.9763388G>TCA394705957GRIN2Ac.4156C>A (p.Pro1386Thr)
c.3342C>A (p.Thr1114=)
n.3406C>A
c.3685C>A (p.Pro1229Thr)
c.*1526C>A (n.*1526C>A)
c.3745C>A (p.Pro1249Thr)
n.3452C>A
c.3402C>A (p.Thr1134=)
c.3813C>A (p.Thr1271=)
c.3997C>A (p.Pro1333Thr)
c.3898C>A (p.Pro1300Thr)
c.4312C>A (p.Pro1438Thr)
c.3969C>A (p.Thr1323=)
dbSNP
16g.9763389G>ACA394705959GRIN2Ac.4155C>T (p.Asp1385=)
c.3341C>T (p.Thr1114Ile)
n.3405C>T
c.3684C>T (p.Asp1228=)
c.*1525C>T (n.*1525C>T)
c.3744C>T (p.Asp1248=)
n.3451C>T
c.3401C>T (p.Thr1134Ile)
c.3812C>T (p.Thr1271Ile)
c.3996C>T (p.Asp1332=)
c.3897C>T (p.Asp1299=)
c.4311C>T (p.Asp1437=)
c.3968C>T (p.Thr1323Ile)
dbSNP
16g.9763389G>CCA394705960GRIN2Ac.4155C>G (p.Asp1385Glu)
c.3341C>G (p.Thr1114Ser)
n.3405C>G
c.3684C>G (p.Asp1228Glu)
c.*1525C>G (n.*1525C>G)
c.3744C>G (p.Asp1248Glu)
n.3451C>G
c.3401C>G (p.Thr1134Ser)
c.3812C>G (p.Thr1271Ser)
c.3996C>G (p.Asp1332Glu)
c.3897C>G (p.Asp1299Glu)
c.4311C>G (p.Asp1437Glu)
c.3968C>G (p.Thr1323Ser)
dbSNP
16g.9763389G>TCA394705961GRIN2Ac.4155C>A (p.Asp1385Glu)
c.3341C>A (p.Thr1114Asn)
n.3405C>A
c.3684C>A (p.Asp1228Glu)
c.*1525C>A (n.*1525C>A)
c.3744C>A (p.Asp1248Glu)
n.3451C>A
c.3401C>A (p.Thr1134Asn)
c.3812C>A (p.Thr1271Asn)
c.3996C>A (p.Asp1332Glu)
c.3897C>A (p.Asp1299Glu)
c.4311C>A (p.Asp1437Glu)
c.3968C>A (p.Thr1323Asn)
16g.9763390T>ACA394705962GRIN2Ac.4154A>T (p.Asp1385Val)
c.3340A>T (p.Thr1114Ser)
n.3404A>T
c.3683A>T (p.Asp1228Val)
c.*1524A>T (n.*1524A>T)
c.3743A>T (p.Asp1248Val)
n.3450A>T
c.3400A>T (p.Thr1134Ser)
c.3811A>T (p.Thr1271Ser)
c.3995A>T (p.Asp1332Val)
c.3896A>T (p.Asp1299Val)
c.4310A>T (p.Asp1437Val)
c.3967A>T (p.Thr1323Ser)
dbSNP
16g.9763390T>CCA394705963GRIN2Ac.4154A>G (p.Asp1385Gly)
c.3340A>G (p.Thr1114Ala)
n.3404A>G
c.3683A>G (p.Asp1228Gly)
c.*1524A>G (n.*1524A>G)
c.3743A>G (p.Asp1248Gly)
n.3450A>G
c.3400A>G (p.Thr1134Ala)
c.3811A>G (p.Thr1271Ala)
c.3995A>G (p.Asp1332Gly)
c.3896A>G (p.Asp1299Gly)
c.4310A>G (p.Asp1437Gly)
c.3967A>G (p.Thr1323Ala)
dbSNP gnomAD v4
16g.9763390T>GCA394705964GRIN2Ac.4154A>C (p.Asp1385Ala)
c.3340A>C (p.Thr1114Pro)
n.3404A>C
c.3683A>C (p.Asp1228Ala)
c.*1524A>C (n.*1524A>C)
c.3743A>C (p.Asp1248Ala)
n.3450A>C
c.3400A>C (p.Thr1134Pro)
c.3811A>C (p.Thr1271Pro)
c.3995A>C (p.Asp1332Ala)
c.3896A>C (p.Asp1299Ala)
c.4310A>C (p.Asp1437Ala)
c.3967A>C (p.Thr1323Pro)
dbSNP
16g.9763391C>ACA394705965GRIN2Ac.4153G>T (p.Asp1385Tyr)
c.3339G>T (p.Arg1113=)
n.3403G>T
c.3682G>T (p.Asp1228Tyr)
c.*1523G>T (n.*1523G>T)
c.3742G>T (p.Asp1248Tyr)
n.3449G>T
c.3399G>T (p.Arg1133=)
c.3810G>T (p.Arg1270=)
c.3994G>T (p.Asp1332Tyr)
c.3895G>T (p.Asp1299Tyr)
c.4309G>T (p.Asp1437Tyr)
c.3966G>T (p.Arg1322=)
dbSNP
16g.9763391C=CA2206692696GRIN2Ac.4153G= (p.Asp1385=)
c.3339G= (p.Arg1113=)
n.3403G=
c.3682G= (p.Asp1228=)
c.*1523G= (n.*1523G=)
c.3742G= (p.Asp1248=)
n.3449G=
c.3399G= (p.Arg1133=)
c.3810G= (p.Arg1270=)
c.3994G= (p.Asp1332=)
c.3895G= (p.Asp1299=)
c.4309G= (p.Asp1437=)
c.3966G= (p.Arg1322=)
16g.9763391C>GCA394705966GRIN2Ac.4153G>C (p.Asp1385His)
c.3339G>C (p.Arg1113=)
n.3403G>C
c.3682G>C (p.Asp1228His)
c.*1523G>C (n.*1523G>C)
c.3742G>C (p.Asp1248His)
n.3449G>C
c.3399G>C (p.Arg1133=)
c.3810G>C (p.Arg1270=)
c.3994G>C (p.Asp1332His)
c.3895G>C (p.Asp1299His)
c.4309G>C (p.Asp1437His)
c.3966G>C (p.Arg1322=)
dbSNP
16g.9763391C>TCA394705967GRIN2Ac.4153G>A (p.Asp1385Asn)
c.3339G>A (p.Arg1113=)
n.3403G>A
c.3682G>A (p.Asp1228Asn)
c.*1523G>A (n.*1523G>A)
c.3742G>A (p.Asp1248Asn)
n.3449G>A
c.3399G>A (p.Arg1133=)
c.3810G>A (p.Arg1270=)
c.3994G>A (p.Asp1332Asn)
c.3895G>A (p.Asp1299Asn)
c.4309G>A (p.Asp1437Asn)
c.3966G>A (p.Arg1322=)
ClinVar dbSNP
16g.9763392C>ACA394705969GRIN2Ac.4152G>T (p.Ser1384=)
c.3338G>T (p.Arg1113Leu)
n.3402G>T
c.3681G>T (p.Ser1227=)
c.*1522G>T (n.*1522G>T)
c.3741G>T (p.Ser1247=)
n.3448G>T
c.3398G>T (p.Arg1133Leu)
c.3809G>T (p.Arg1270Leu)
c.3993G>T (p.Ser1331=)
c.3894G>T (p.Ser1298=)
c.4308G>T (p.Ser1436=)
c.3965G>T (p.Arg1322Leu)
16g.9763392C=CA2206692697GRIN2Ac.4152G= (p.Ser1384=)
c.3338G= (p.Arg1113=)
n.3402G=
c.3681G= (p.Ser1227=)
c.*1522G= (n.*1522G=)
c.3741G= (p.Ser1247=)
n.3448G=
c.3398G= (p.Arg1133=)
c.3809G= (p.Arg1270=)
c.3993G= (p.Ser1331=)
c.3894G= (p.Ser1298=)
c.4308G= (p.Ser1436=)
c.3965G= (p.Arg1322=)
16g.9763392C>GCA394705968GRIN2Ac.4152G>C (p.Ser1384=)
c.3338G>C (p.Arg1113Pro)
n.3402G>C
c.3681G>C (p.Ser1227=)
c.*1522G>C (n.*1522G>C)
c.3741G>C (p.Ser1247=)
n.3448G>C
c.3398G>C (p.Arg1133Pro)
c.3809G>C (p.Arg1270Pro)
c.3993G>C (p.Ser1331=)
c.3894G>C (p.Ser1298=)
c.4308G>C (p.Ser1436=)
c.3965G>C (p.Arg1322Pro)
dbSNP
16g.9763392C>TCA7896205GRIN2Ac.4152G>A (p.Ser1384=)
c.3338G>A (p.Arg1113Gln)
n.3402G>A
c.3681G>A (p.Ser1227=)
c.*1522G>A (n.*1522G>A)
c.3741G>A (p.Ser1247=)
n.3448G>A
c.3398G>A (p.Arg1133Gln)
c.3809G>A (p.Arg1270Gln)
c.3993G>A (p.Ser1331=)
c.3894G>A (p.Ser1298=)
c.4308G>A (p.Ser1436=)
c.3965G>A (p.Arg1322Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
16g.9763393G>ACA277536075GRIN2Ac.4151C>T (p.Ser1384Leu)
c.3337C>T (p.Arg1113Trp)
n.3401C>T
c.3680C>T (p.Ser1227Leu)
c.*1521C>T (n.*1521C>T)
c.3740C>T (p.Ser1247Leu)
n.3447C>T
c.3397C>T (p.Arg1133Trp)
c.3808C>T (p.Arg1270Trp)
c.3992C>T (p.Ser1331Leu)
c.3893C>T (p.Ser1298Leu)
c.4307C>T (p.Ser1436Leu)
c.3964C>T (p.Arg1322Trp)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.9763393G>CCA394705970GRIN2Ac.4151C>G (p.Ser1384Trp)
c.3337C>G (p.Arg1113Gly)
n.3401C>G
c.3680C>G (p.Ser1227Trp)
c.*1521C>G (n.*1521C>G)
c.3740C>G (p.Ser1247Trp)
n.3447C>G
c.3397C>G (p.Arg1133Gly)
c.3808C>G (p.Arg1270Gly)
c.3992C>G (p.Ser1331Trp)
c.3893C>G (p.Ser1298Trp)
c.4307C>G (p.Ser1436Trp)
c.3964C>G (p.Arg1322Gly)
dbSNP
16g.9763393G=CA2206692698GRIN2Ac.4151C= (p.Ser1384=)
c.3337C= (p.Arg1113=)
n.3401C=
c.3680C= (p.Ser1227=)
c.*1521C= (n.*1521C=)
c.3740C= (p.Ser1247=)
n.3447C=
c.3397C= (p.Arg1133=)
c.3808C= (p.Arg1270=)
c.3992C= (p.Ser1331=)
c.3893C= (p.Ser1298=)
c.4307C= (p.Ser1436=)
c.3964C= (p.Arg1322=)
16g.9763393G>TCA394705971GRIN2Ac.4151C>A (p.Ser1384Ter)
c.3337C>A (p.Arg1113=)
n.3401C>A
c.3680C>A (p.Ser1227Ter)
c.*1521C>A (n.*1521C>A)
c.3740C>A (p.Ser1247Ter)
n.3447C>A
c.3397C>A (p.Arg1133=)
c.3808C>A (p.Arg1270=)
c.3992C>A (p.Ser1331Ter)
c.3893C>A (p.Ser1298Ter)
c.4307C>A (p.Ser1436Ter)
c.3964C>A (p.Arg1322=)
dbSNP
16g.9763394A>CCA394705972GRIN2Ac.4150T>G (p.Ser1384Ala)
c.3336T>G (p.Pro1112=)
n.3400T>G
c.3679T>G (p.Ser1227Ala)
c.*1520T>G (n.*1520T>G)
c.3739T>G (p.Ser1247Ala)
n.3446T>G
c.3396T>G (p.Pro1132=)
c.3807T>G (p.Pro1269=)
c.3991T>G (p.Ser1331Ala)
c.3892T>G (p.Ser1298Ala)
c.4306T>G (p.Ser1436Ala)
c.3963T>G (p.Pro1321=)
16g.9763394A>GCA394705973GRIN2Ac.4150T>C (p.Ser1384Pro)
c.3336T>C (p.Pro1112=)
n.3400T>C
c.3679T>C (p.Ser1227Pro)
c.*1520T>C (n.*1520T>C)
c.3739T>C (p.Ser1247Pro)
n.3446T>C
c.3396T>C (p.Pro1132=)
c.3807T>C (p.Pro1269=)
c.3991T>C (p.Ser1331Pro)
c.3892T>C (p.Ser1298Pro)
c.4306T>C (p.Ser1436Pro)
c.3963T>C (p.Pro1321=)
gnomAD v4
16g.9763394A>TCA394705974GRIN2Ac.4150T>A (p.Ser1384Thr)
c.3336T>A (p.Pro1112=)
n.3400T>A
c.3679T>A (p.Ser1227Thr)
c.*1520T>A (n.*1520T>A)
c.3739T>A (p.Ser1247Thr)
n.3446T>A
c.3396T>A (p.Pro1132=)
c.3807T>A (p.Pro1269=)
c.3991T>A (p.Ser1331Thr)
c.3892T>A (p.Ser1298Thr)
c.4306T>A (p.Ser1436Thr)
c.3963T>A (p.Pro1321=)
dbSNP
16g.9763395G>ACA394705975GRIN2Ac.4149C>T (p.Pro1383=)
c.3335C>T (p.Pro1112Leu)
n.3399C>T
c.3678C>T (p.Pro1226=)
c.*1519C>T (n.*1519C>T)
c.3738C>T (p.Pro1246=)
n.3445C>T
c.3395C>T (p.Pro1132Leu)
c.3806C>T (p.Pro1269Leu)
c.3990C>T (p.Pro1330=)
c.3891C>T (p.Pro1297=)
c.4305C>T (p.Pro1435=)
c.3962C>T (p.Pro1321Leu)
dbSNP
16g.9763395G>CCA394705976GRIN2Ac.4149C>G (p.Pro1383=)
c.3335C>G (p.Pro1112Arg)
n.3399C>G
c.3678C>G (p.Pro1226=)
c.*1519C>G (n.*1519C>G)
c.3738C>G (p.Pro1246=)
n.3445C>G
c.3395C>G (p.Pro1132Arg)
c.3806C>G (p.Pro1269Arg)
c.3990C>G (p.Pro1330=)
c.3891C>G (p.Pro1297=)
c.4305C>G (p.Pro1435=)
c.3962C>G (p.Pro1321Arg)
16g.9763395G>TCA394705977GRIN2Ac.4149C>A (p.Pro1383=)
c.3335C>A (p.Pro1112His)
n.3399C>A
c.3678C>A (p.Pro1226=)
c.*1519C>A (n.*1519C>A)
c.3738C>A (p.Pro1246=)
n.3445C>A
c.3395C>A (p.Pro1132His)
c.3806C>A (p.Pro1269His)
c.3990C>A (p.Pro1330=)
c.3891C>A (p.Pro1297=)
c.4305C>A (p.Pro1435=)
c.3962C>A (p.Pro1321His)
dbSNP
16g.9763396G>ACA394705978GRIN2Ac.4148C>T (p.Pro1383Leu)
c.3334C>T (p.Pro1112Ser)
n.3398C>T
c.3677C>T (p.Pro1226Leu)
c.*1518C>T (n.*1518C>T)
c.3737C>T (p.Pro1246Leu)
n.3444C>T
c.3394C>T (p.Pro1132Ser)
c.3805C>T (p.Pro1269Ser)
c.3989C>T (p.Pro1330Leu)
c.3890C>T (p.Pro1297Leu)
c.4304C>T (p.Pro1435Leu)
c.3961C>T (p.Pro1321Ser)
dbSNP
16g.9763396G>CCA394705979GRIN2Ac.4148C>G (p.Pro1383Arg)
c.3334C>G (p.Pro1112Ala)
n.3398C>G
c.3677C>G (p.Pro1226Arg)
c.*1518C>G (n.*1518C>G)
c.3737C>G (p.Pro1246Arg)
n.3444C>G
c.3394C>G (p.Pro1132Ala)
c.3805C>G (p.Pro1269Ala)
c.3989C>G (p.Pro1330Arg)
c.3890C>G (p.Pro1297Arg)
c.4304C>G (p.Pro1435Arg)
c.3961C>G (p.Pro1321Ala)
16g.9763396G>TCA394705980GRIN2Ac.4148C>A (p.Pro1383His)
c.3334C>A (p.Pro1112Thr)
n.3398C>A
c.3677C>A (p.Pro1226His)
c.*1518C>A (n.*1518C>A)
c.3737C>A (p.Pro1246His)
n.3444C>A
c.3394C>A (p.Pro1132Thr)
c.3805C>A (p.Pro1269Thr)
c.3989C>A (p.Pro1330His)
c.3890C>A (p.Pro1297His)
c.4304C>A (p.Pro1435His)
c.3961C>A (p.Pro1321Thr)
dbSNP
16g.9763397G>ACA277536082GRIN2Ac.4147C>T (p.Pro1383Ser)
c.3333C>T (p.Ala1111=)
n.3397C>T
c.3676C>T (p.Pro1226Ser)
c.*1517C>T (n.*1517C>T)
c.3736C>T (p.Pro1246Ser)
n.3443C>T
c.3393C>T (p.Ala1131=)
c.3804C>T (p.Ala1268=)
c.3988C>T (p.Pro1330Ser)
c.3889C>T (p.Pro1297Ser)
c.4303C>T (p.Pro1435Ser)
c.3960C>T (p.Ala1320=)
dbSNP
16g.9763397G>CCA394705981GRIN2Ac.4147C>G (p.Pro1383Ala)
c.3333C>G (p.Ala1111=)
n.3397C>G
c.3676C>G (p.Pro1226Ala)
c.*1517C>G (n.*1517C>G)
c.3736C>G (p.Pro1246Ala)
n.3443C>G
c.3393C>G (p.Ala1131=)
c.3804C>G (p.Ala1268=)
c.3988C>G (p.Pro1330Ala)
c.3889C>G (p.Pro1297Ala)
c.4303C>G (p.Pro1435Ala)
c.3960C>G (p.Ala1320=)
dbSNP
16g.9763397G=CA2206692699GRIN2Ac.4147C= (p.Pro1383=)
c.3333C= (p.Ala1111=)
n.3397C=
c.3676C= (p.Pro1226=)
c.*1517C= (n.*1517C=)
c.3736C= (p.Pro1246=)
n.3443C=
c.3393C= (p.Ala1131=)
c.3804C= (p.Ala1268=)
c.3988C= (p.Pro1330=)
c.3889C= (p.Pro1297=)
c.4303C= (p.Pro1435=)
c.3960C= (p.Ala1320=)
16g.9763397G>TCA394705982GRIN2Ac.4147C>A (p.Pro1383Thr)
c.3333C>A (p.Ala1111=)
n.3397C>A
c.3676C>A (p.Pro1226Thr)
c.*1517C>A (n.*1517C>A)
c.3736C>A (p.Pro1246Thr)
n.3443C>A
c.3393C>A (p.Ala1131=)
c.3804C>A (p.Ala1268=)
c.3988C>A (p.Pro1330Thr)
c.3889C>A (p.Pro1297Thr)
c.4303C>A (p.Pro1435Thr)
c.3960C>A (p.Ala1320=)
dbSNP

Number of alleles fetched