Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.9763108_9769129del | CA915949116 | GRIN2A | c.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 |
16 | g.9763239_9763244del | CA2631674834 | GRIN2A | c.4305_4310del (p.Lys1435_Asn1436del) c.*116_*121del (n.*116_*121del) n.3555_3560del c.3834_3839del (p.Lys1278_Asn1279del) c.*1675_*1680del (n.*1675_*1680del) c.3894_3899del (p.Lys1298_Asn1299del) n.3601_3606del c.4146_4151del (p.Lys1382_Asn1383del) c.4047_4052del (p.Lys1349_Asn1350del) c.4461_4466del (p.Lys1487_Asn1488del) | gnomAD v4 |
16 | g.9763241T>A | CA394705290 | GRIN2A | c.4303A>T (p.Lys1435Ter) c.*114A>T (n.*114A>T) n.3553A>T c.3832A>T (p.Lys1278Ter) c.*1673A>T (n.*1673A>T) c.3892A>T (p.Lys1298Ter) n.3599A>T c.4144A>T (p.Lys1382Ter) c.4045A>T (p.Lys1349Ter) c.4459A>T (p.Lys1487Ter) | |
16 | g.9763241T>C | CA394705286 | GRIN2A | c.4303A>G (p.Lys1435Glu) c.*114A>G (n.*114A>G) n.3553A>G c.3832A>G (p.Lys1278Glu) c.*1673A>G (n.*1673A>G) c.3892A>G (p.Lys1298Glu) n.3599A>G c.4144A>G (p.Lys1382Glu) c.4045A>G (p.Lys1349Glu) c.4459A>G (p.Lys1487Glu) | |
16 | g.9763241T>G | CA394705288 | GRIN2A | c.4303A>C (p.Lys1435Gln) c.*114A>C (n.*114A>C) n.3553A>C c.3832A>C (p.Lys1278Gln) c.*1673A>C (n.*1673A>C) c.3892A>C (p.Lys1298Gln) n.3599A>C c.4144A>C (p.Lys1382Gln) c.4045A>C (p.Lys1349Gln) c.4459A>C (p.Lys1487Gln) | |
16 | g.9763242A>C | CA394705292 | GRIN2A | c.4302T>G (p.Asn1434Lys) c.*113T>G (n.*113T>G) n.3552T>G c.3831T>G (p.Asn1277Lys) c.*1672T>G (n.*1672T>G) c.3891T>G (p.Asn1297Lys) n.3598T>G c.4143T>G (p.Asn1381Lys) c.4044T>G (p.Asn1348Lys) c.4458T>G (p.Asn1486Lys) | |
16 | g.9763242A>G | CA493692494 | GRIN2A | c.4302T>C (p.Asn1434=) c.*113T>C (n.*113T>C) n.3552T>C c.3831T>C (p.Asn1277=) c.*1672T>C (n.*1672T>C) c.3891T>C (p.Asn1297=) n.3598T>C c.4143T>C (p.Asn1381=) c.4044T>C (p.Asn1348=) c.4458T>C (p.Asn1486=) | gnomAD v4 |
16 | g.9763242A>T | CA394705294 | GRIN2A | c.4302T>A (p.Asn1434Lys) c.*113T>A (n.*113T>A) n.3552T>A c.3831T>A (p.Asn1277Lys) c.*1672T>A (n.*1672T>A) c.3891T>A (p.Asn1297Lys) n.3598T>A c.4143T>A (p.Asn1381Lys) c.4044T>A (p.Asn1348Lys) c.4458T>A (p.Asn1486Lys) | |
16 | g.9763243T>A | CA394705297 | GRIN2A | c.4301A>T (p.Asn1434Ile) c.*112A>T (n.*112A>T) n.3551A>T c.3830A>T (p.Asn1277Ile) c.*1671A>T (n.*1671A>T) c.3890A>T (p.Asn1297Ile) n.3597A>T c.4142A>T (p.Asn1381Ile) c.4043A>T (p.Asn1348Ile) c.4457A>T (p.Asn1486Ile) | |
16 | g.9763243T>C | CA394705298 | GRIN2A | c.4301A>G (p.Asn1434Ser) c.*112A>G (n.*112A>G) n.3551A>G c.3830A>G (p.Asn1277Ser) c.*1671A>G (n.*1671A>G) c.3890A>G (p.Asn1297Ser) n.3597A>G c.4142A>G (p.Asn1381Ser) c.4043A>G (p.Asn1348Ser) c.4457A>G (p.Asn1486Ser) | |
16 | g.9763243T>G | CA394705300 | GRIN2A | c.4301A>C (p.Asn1434Thr) c.*112A>C (n.*112A>C) n.3551A>C c.3830A>C (p.Asn1277Thr) c.*1671A>C (n.*1671A>C) c.3890A>C (p.Asn1297Thr) n.3597A>C c.4142A>C (p.Asn1381Thr) c.4043A>C (p.Asn1348Thr) c.4457A>C (p.Asn1486Thr) | |
16 | g.9763244T>A | CA394705306 | GRIN2A | c.4300A>T (p.Asn1434Tyr) c.*111A>T (n.*111A>T) n.3550A>T c.3829A>T (p.Asn1277Tyr) c.*1670A>T (n.*1670A>T) c.3889A>T (p.Asn1297Tyr) n.3596A>T c.4141A>T (p.Asn1381Tyr) c.4042A>T (p.Asn1348Tyr) c.4456A>T (p.Asn1486Tyr) | |
16 | g.9763244T>C | CA394705304 | GRIN2A | c.4300A>G (p.Asn1434Asp) c.*111A>G (n.*111A>G) n.3550A>G c.3829A>G (p.Asn1277Asp) c.*1670A>G (n.*1670A>G) c.3889A>G (p.Asn1297Asp) n.3596A>G c.4141A>G (p.Asn1381Asp) c.4042A>G (p.Asn1348Asp) c.4456A>G (p.Asn1486Asp) | |
16 | g.9763244T>G | CA394705302 | GRIN2A | c.4300A>C (p.Asn1434His) c.*111A>C (n.*111A>C) n.3550A>C c.3829A>C (p.Asn1277His) c.*1670A>C (n.*1670A>C) c.3889A>C (p.Asn1297His) n.3596A>C c.4141A>C (p.Asn1381His) c.4042A>C (p.Asn1348His) c.4456A>C (p.Asn1486His) | |
16 | g.9763245T>A | CA493692497 | GRIN2A | c.4299A>T (p.Ala1433=) c.*110A>T (n.*110A>T) n.3549A>T c.3828A>T (p.Ala1276=) c.*1669A>T (n.*1669A>T) c.3888A>T (p.Ala1296=) n.3595A>T c.4140A>T (p.Ala1380=) c.4041A>T (p.Ala1347=) c.4455A>T (p.Ala1485=) | |
16 | g.9763245T>C | CA493692498 | GRIN2A | c.4299A>G (p.Ala1433=) c.*110A>G (n.*110A>G) n.3549A>G c.3828A>G (p.Ala1276=) c.*1669A>G (n.*1669A>G) c.3888A>G (p.Ala1296=) n.3595A>G c.4140A>G (p.Ala1380=) c.4041A>G (p.Ala1347=) c.4455A>G (p.Ala1485=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.9763245T>G | CA493692499 | GRIN2A | c.4299A>C (p.Ala1433=) c.*110A>C (n.*110A>C) n.3549A>C c.3828A>C (p.Ala1276=) c.*1669A>C (n.*1669A>C) c.3888A>C (p.Ala1296=) n.3595A>C c.4140A>C (p.Ala1380=) c.4041A>C (p.Ala1347=) c.4455A>C (p.Ala1485=) | |
16 | g.9763245T= | CA2206692627 | GRIN2A | c.4299A= (p.Ala1433=) c.*110A= (n.*110A=) n.3549A= c.3828A= (p.Ala1276=) c.*1669A= (n.*1669A=) c.3888A= (p.Ala1296=) n.3595A= c.4140A= (p.Ala1380=) c.4041A= (p.Ala1347=) c.4455A= (p.Ala1485=) | |
16 | g.9763246G>A | CA394705308 | GRIN2A | c.4298C>T (p.Ala1433Val) c.*109C>T (n.*109C>T) n.3548C>T c.3827C>T (p.Ala1276Val) c.*1668C>T (n.*1668C>T) c.3887C>T (p.Ala1296Val) n.3594C>T c.4139C>T (p.Ala1380Val) c.4040C>T (p.Ala1347Val) c.4454C>T (p.Ala1485Val) | COSMIC |
16 | g.9763246G>C | CA394705310 | GRIN2A | c.4298C>G (p.Ala1433Gly) c.*109C>G (n.*109C>G) n.3548C>G c.3827C>G (p.Ala1276Gly) c.*1668C>G (n.*1668C>G) c.3887C>G (p.Ala1296Gly) n.3594C>G c.4139C>G (p.Ala1380Gly) c.4040C>G (p.Ala1347Gly) c.4454C>G (p.Ala1485Gly) | |
16 | g.9763246G>T | CA394705312 | GRIN2A | c.4298C>A (p.Ala1433Glu) c.*109C>A (n.*109C>A) n.3548C>A c.3827C>A (p.Ala1276Glu) c.*1668C>A (n.*1668C>A) c.3887C>A (p.Ala1296Glu) n.3594C>A c.4139C>A (p.Ala1380Glu) c.4040C>A (p.Ala1347Glu) c.4454C>A (p.Ala1485Glu) | |
16 | g.9763247C>A | CA394705314 | GRIN2A | c.4297G>T (p.Ala1433Ser) c.*108G>T (n.*108G>T) n.3547G>T c.3826G>T (p.Ala1276Ser) c.*1667G>T (n.*1667G>T) c.3886G>T (p.Ala1296Ser) n.3593G>T c.4138G>T (p.Ala1380Ser) c.4039G>T (p.Ala1347Ser) c.4453G>T (p.Ala1485Ser) | |
16 | g.9763247C>G | CA394705315 | GRIN2A | c.4297G>C (p.Ala1433Pro) c.*108G>C (n.*108G>C) n.3547G>C c.3826G>C (p.Ala1276Pro) c.*1667G>C (n.*1667G>C) c.3886G>C (p.Ala1296Pro) n.3593G>C c.4138G>C (p.Ala1380Pro) c.4039G>C (p.Ala1347Pro) c.4453G>C (p.Ala1485Pro) | |
16 | g.9763247C>T | CA394705317 | GRIN2A | c.4297G>A (p.Ala1433Thr) c.*108G>A (n.*108G>A) n.3547G>A c.3826G>A (p.Ala1276Thr) c.*1667G>A (n.*1667G>A) c.3886G>A (p.Ala1296Thr) n.3593G>A c.4138G>A (p.Ala1380Thr) c.4039G>A (p.Ala1347Thr) c.4453G>A (p.Ala1485Thr) | dbSNP gnomAD v4 |
16 | g.9763248A>C | CA493692506 | GRIN2A | c.4296T>G (p.Ala1432=) c.*107T>G (n.*107T>G) n.3546T>G c.3825T>G (p.Ala1275=) c.*1666T>G (n.*1666T>G) c.3885T>G (p.Ala1295=) n.3592T>G c.4137T>G (p.Ala1379=) c.4038T>G (p.Ala1346=) c.4452T>G (p.Ala1484=) | gnomAD v4 |
16 | g.9763248A>G | CA493692504 | GRIN2A | c.4296T>C (p.Ala1432=) c.*107T>C (n.*107T>C) n.3546T>C c.3825T>C (p.Ala1275=) c.*1666T>C (n.*1666T>C) c.3885T>C (p.Ala1295=) n.3592T>C c.4137T>C (p.Ala1379=) c.4038T>C (p.Ala1346=) c.4452T>C (p.Ala1484=) | gnomAD v4 |
16 | g.9763248A>T | CA493692505 | GRIN2A | c.4296T>A (p.Ala1432=) c.*107T>A (n.*107T>A) n.3546T>A c.3825T>A (p.Ala1275=) c.*1666T>A (n.*1666T>A) c.3885T>A (p.Ala1295=) n.3592T>A c.4137T>A (p.Ala1379=) c.4038T>A (p.Ala1346=) c.4452T>A (p.Ala1484=) | |
16 | g.9763249G>A | CA394705323 | GRIN2A | c.4295C>T (p.Ala1432Val) c.*106C>T (n.*106C>T) n.3545C>T c.3824C>T (p.Ala1275Val) c.*1665C>T (n.*1665C>T) c.3884C>T (p.Ala1295Val) n.3591C>T c.4136C>T (p.Ala1379Val) c.4037C>T (p.Ala1346Val) c.4451C>T (p.Ala1484Val) | dbSNP |
16 | g.9763249G>C | CA277535842 | GRIN2A | c.4295C>G (p.Ala1432Gly) c.*106C>G (n.*106C>G) n.3545C>G c.3824C>G (p.Ala1275Gly) c.*1665C>G (n.*1665C>G) c.3884C>G (p.Ala1295Gly) n.3591C>G c.4136C>G (p.Ala1379Gly) c.4037C>G (p.Ala1346Gly) c.4451C>G (p.Ala1484Gly) | dbSNP |
16 | g.9763249G= | CA2206692628 | GRIN2A | c.4295C= (p.Ala1432=) c.*106C= (n.*106C=) n.3545C= c.3824C= (p.Ala1275=) c.*1665C= (n.*1665C=) c.3884C= (p.Ala1295=) n.3591C= c.4136C= (p.Ala1379=) c.4037C= (p.Ala1346=) c.4451C= (p.Ala1484=) | |
16 | g.9763249G>T | CA394705322 | GRIN2A | c.4295C>A (p.Ala1432Asp) c.*106C>A (n.*106C>A) n.3545C>A c.3824C>A (p.Ala1275Asp) c.*1665C>A (n.*1665C>A) c.3884C>A (p.Ala1295Asp) n.3591C>A c.4136C>A (p.Ala1379Asp) c.4037C>A (p.Ala1346Asp) c.4451C>A (p.Ala1484Asp) | |
16 | g.9763250C>A | CA394705325 | GRIN2A | c.4294G>T (p.Ala1432Ser) c.*105G>T (n.*105G>T) n.3544G>T c.3823G>T (p.Ala1275Ser) c.*1664G>T (n.*1664G>T) c.3883G>T (p.Ala1295Ser) n.3590G>T c.4135G>T (p.Ala1379Ser) c.4036G>T (p.Ala1346Ser) c.4450G>T (p.Ala1484Ser) | |
16 | g.9763250C= | CA2206692629 | GRIN2A | c.4294G= (p.Ala1432=) c.*105G= (n.*105G=) n.3544G= c.3823G= (p.Ala1275=) c.*1664G= (n.*1664G=) c.3883G= (p.Ala1295=) n.3590G= c.4135G= (p.Ala1379=) c.4036G= (p.Ala1346=) c.4450G= (p.Ala1484=) | |
16 | g.9763250C>G | CA394705327 | GRIN2A | c.4294G>C (p.Ala1432Pro) c.*105G>C (n.*105G>C) n.3544G>C c.3823G>C (p.Ala1275Pro) c.*1664G>C (n.*1664G>C) c.3883G>C (p.Ala1295Pro) n.3590G>C c.4135G>C (p.Ala1379Pro) c.4036G>C (p.Ala1346Pro) c.4450G>C (p.Ala1484Pro) | |
16 | g.9763250C>T | CA394705328 | GRIN2A | c.4294G>A (p.Ala1432Thr) c.*105G>A (n.*105G>A) n.3544G>A c.3823G>A (p.Ala1275Thr) c.*1664G>A (n.*1664G>A) c.3883G>A (p.Ala1295Thr) n.3590G>A c.4135G>A (p.Ala1379Thr) c.4036G>A (p.Ala1346Thr) c.4450G>A (p.Ala1484Thr) | dbSNP |
16 | g.9763251A= | CA2206692630 | GRIN2A | c.4293T= (p.Tyr1431=) c.*104T= (n.*104T=) n.3543T= c.3822T= (p.Tyr1274=) c.*1663T= (n.*1663T=) c.3882T= (p.Tyr1294=) n.3589T= c.4134T= (p.Tyr1378=) c.4035T= (p.Tyr1345=) c.4449T= (p.Tyr1483=) | |
16 | g.9763251A>C | CA394705331 | GRIN2A | c.4293T>G (p.Tyr1431Ter) c.*104T>G (n.*104T>G) n.3543T>G c.3822T>G (p.Tyr1274Ter) c.*1663T>G (n.*1663T>G) c.3882T>G (p.Tyr1294Ter) n.3589T>G c.4134T>G (p.Tyr1378Ter) c.4035T>G (p.Tyr1345Ter) c.4449T>G (p.Tyr1483Ter) | |
16 | g.9763251A>G | CA7896182 | GRIN2A | c.4293T>C (p.Tyr1431=) c.*104T>C (n.*104T>C) n.3543T>C c.3822T>C (p.Tyr1274=) c.*1663T>C (n.*1663T>C) c.3882T>C (p.Tyr1294=) n.3589T>C c.4134T>C (p.Tyr1378=) c.4035T>C (p.Tyr1345=) c.4449T>C (p.Tyr1483=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.9763251A>T | CA394705333 | GRIN2A | c.4293T>A (p.Tyr1431Ter) c.*104T>A (n.*104T>A) n.3543T>A c.3822T>A (p.Tyr1274Ter) c.*1663T>A (n.*1663T>A) c.3882T>A (p.Tyr1294Ter) n.3589T>A c.4134T>A (p.Tyr1378Ter) c.4035T>A (p.Tyr1345Ter) c.4449T>A (p.Tyr1483Ter) | |
16 | g.9763252T>A | CA394705335 | GRIN2A | c.4292A>T (p.Tyr1431Phe) c.*103A>T (n.*103A>T) n.3542A>T c.3821A>T (p.Tyr1274Phe) c.*1662A>T (n.*1662A>T) c.3881A>T (p.Tyr1294Phe) n.3588A>T c.4133A>T (p.Tyr1378Phe) c.4034A>T (p.Tyr1345Phe) c.4448A>T (p.Tyr1483Phe) | |
16 | g.9763252T>C | CA394705337 | GRIN2A | c.4292A>G (p.Tyr1431Cys) c.*103A>G (n.*103A>G) n.3542A>G c.3821A>G (p.Tyr1274Cys) c.*1662A>G (n.*1662A>G) c.3881A>G (p.Tyr1294Cys) n.3588A>G c.4133A>G (p.Tyr1378Cys) c.4034A>G (p.Tyr1345Cys) c.4448A>G (p.Tyr1483Cys) | |
16 | g.9763252T>G | CA394705338 | GRIN2A | c.4292A>C (p.Tyr1431Ser) c.*103A>C (n.*103A>C) n.3542A>C c.3821A>C (p.Tyr1274Ser) c.*1662A>C (n.*1662A>C) c.3881A>C (p.Tyr1294Ser) n.3588A>C c.4133A>C (p.Tyr1378Ser) c.4034A>C (p.Tyr1345Ser) c.4448A>C (p.Tyr1483Ser) | |
16 | g.9763253A>C | CA394705342 | GRIN2A | c.4291T>G (p.Tyr1431Asp) c.*102T>G (n.*102T>G) n.3541T>G c.3820T>G (p.Tyr1274Asp) c.*1661T>G (n.*1661T>G) c.3880T>G (p.Tyr1294Asp) n.3587T>G c.4132T>G (p.Tyr1378Asp) c.4033T>G (p.Tyr1345Asp) c.4447T>G (p.Tyr1483Asp) | gnomAD v4 |
16 | g.9763253A>G | CA394705344 | GRIN2A | c.4291T>C (p.Tyr1431His) c.*102T>C (n.*102T>C) n.3541T>C c.3820T>C (p.Tyr1274His) c.*1661T>C (n.*1661T>C) c.3880T>C (p.Tyr1294His) n.3587T>C c.4132T>C (p.Tyr1378His) c.4033T>C (p.Tyr1345His) c.4447T>C (p.Tyr1483His) | |
16 | g.9763253A>T | CA394705346 | GRIN2A | c.4291T>A (p.Tyr1431Asn) c.*102T>A (n.*102T>A) n.3541T>A c.3820T>A (p.Tyr1274Asn) c.*1661T>A (n.*1661T>A) c.3880T>A (p.Tyr1294Asn) n.3587T>A c.4132T>A (p.Tyr1378Asn) c.4033T>A (p.Tyr1345Asn) c.4447T>A (p.Tyr1483Asn) | |
16 | g.9763254A= | CA2206692631 | GRIN2A | c.4290T= (p.Pro1430=) c.*101T= (n.*101T=) n.3540T= c.3819T= (p.Pro1273=) c.*1660T= (n.*1660T=) c.3879T= (p.Pro1293=) n.3586T= c.4131T= (p.Pro1377=) c.4032T= (p.Pro1344=) c.4446T= (p.Pro1482=) | |
16 | g.9763254A>C | CA7896183 | GRIN2A | c.4290T>G (p.Pro1430=) c.*101T>G (n.*101T>G) n.3540T>G c.3819T>G (p.Pro1273=) c.*1660T>G (n.*1660T>G) c.3879T>G (p.Pro1293=) n.3586T>G c.4131T>G (p.Pro1377=) c.4032T>G (p.Pro1344=) c.4446T>G (p.Pro1482=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.9763254A>G | CA493692513 | GRIN2A | c.4290T>C (p.Pro1430=) c.*101T>C (n.*101T>C) n.3540T>C c.3819T>C (p.Pro1273=) c.*1660T>C (n.*1660T>C) c.3879T>C (p.Pro1293=) n.3586T>C c.4131T>C (p.Pro1377=) c.4032T>C (p.Pro1344=) c.4446T>C (p.Pro1482=) | |
16 | g.9763254A>T | CA493692514 | GRIN2A | c.4290T>A (p.Pro1430=) c.*101T>A (n.*101T>A) n.3540T>A c.3819T>A (p.Pro1273=) c.*1660T>A (n.*1660T>A) c.3879T>A (p.Pro1293=) n.3586T>A c.4131T>A (p.Pro1377=) c.4032T>A (p.Pro1344=) c.4446T>A (p.Pro1482=) | |
16 | g.9763255G>A | CA394705350 | GRIN2A | c.4289C>T (p.Pro1430Leu) c.*100C>T (n.*100C>T) n.3539C>T c.3818C>T (p.Pro1273Leu) c.*1659C>T (n.*1659C>T) c.3878C>T (p.Pro1293Leu) n.3585C>T c.4130C>T (p.Pro1377Leu) c.4031C>T (p.Pro1344Leu) c.4445C>T (p.Pro1482Leu) | |
16 | g.9763255G>C | CA394705354 | GRIN2A | c.4289C>G (p.Pro1430Arg) c.*100C>G (n.*100C>G) n.3539C>G c.3818C>G (p.Pro1273Arg) c.*1659C>G (n.*1659C>G) c.3878C>G (p.Pro1293Arg) n.3585C>G c.4130C>G (p.Pro1377Arg) c.4031C>G (p.Pro1344Arg) c.4445C>G (p.Pro1482Arg) | gnomAD v4 |
16 | g.9763255G>T | CA394705352 | GRIN2A | c.4289C>A (p.Pro1430His) c.*100C>A (n.*100C>A) n.3539C>A c.3818C>A (p.Pro1273His) c.*1659C>A (n.*1659C>A) c.3878C>A (p.Pro1293His) n.3585C>A c.4130C>A (p.Pro1377His) c.4031C>A (p.Pro1344His) c.4445C>A (p.Pro1482His) | |
16 | g.9763256G>A | CA394705356 | GRIN2A | c.4288C>T (p.Pro1430Ser) c.*99C>T (n.*99C>T) n.3538C>T c.3817C>T (p.Pro1273Ser) c.*1658C>T (n.*1658C>T) c.3877C>T (p.Pro1293Ser) n.3584C>T c.4129C>T (p.Pro1377Ser) c.4030C>T (p.Pro1344Ser) c.4444C>T (p.Pro1482Ser) | dbSNP gnomAD v4 |
16 | g.9763256G>C | CA394705360 | GRIN2A | c.4288C>G (p.Pro1430Ala) c.*99C>G (n.*99C>G) n.3538C>G c.3817C>G (p.Pro1273Ala) c.*1658C>G (n.*1658C>G) c.3877C>G (p.Pro1293Ala) n.3584C>G c.4129C>G (p.Pro1377Ala) c.4030C>G (p.Pro1344Ala) c.4444C>G (p.Pro1482Ala) | |
16 | g.9763256G>T | CA394705358 | GRIN2A | c.4288C>A (p.Pro1430Thr) c.*99C>A (n.*99C>A) n.3538C>A c.3817C>A (p.Pro1273Thr) c.*1658C>A (n.*1658C>A) c.3877C>A (p.Pro1293Thr) n.3584C>A c.4129C>A (p.Pro1377Thr) c.4030C>A (p.Pro1344Thr) c.4444C>A (p.Pro1482Thr) | |
16 | g.9763257C>A | CA394705362 | GRIN2A | c.4287G>T (p.Met1429Ile) c.*98G>T (n.*98G>T) n.3537G>T c.3816G>T (p.Met1272Ile) c.*1657G>T (n.*1657G>T) c.3876G>T (p.Met1292Ile) n.3583G>T c.4128G>T (p.Met1376Ile) c.4029G>T (p.Met1343Ile) c.4443G>T (p.Met1481Ile) | |
16 | g.9763257C>G | CA394705364 | GRIN2A | c.4287G>C (p.Met1429Ile) c.*98G>C (n.*98G>C) n.3537G>C c.3816G>C (p.Met1272Ile) c.*1657G>C (n.*1657G>C) c.3876G>C (p.Met1292Ile) n.3583G>C c.4128G>C (p.Met1376Ile) c.4029G>C (p.Met1343Ile) c.4443G>C (p.Met1481Ile) | |
16 | g.9763257C>T | CA394705366 | GRIN2A | c.4287G>A (p.Met1429Ile) c.*98G>A (n.*98G>A) n.3537G>A c.3816G>A (p.Met1272Ile) c.*1657G>A (n.*1657G>A) c.3876G>A (p.Met1292Ile) n.3583G>A c.4128G>A (p.Met1376Ile) c.4029G>A (p.Met1343Ile) c.4443G>A (p.Met1481Ile) | |
16 | g.9763258A>C | CA394705369 | GRIN2A | c.4286T>G (p.Met1429Arg) c.*97T>G (n.*97T>G) n.3536T>G c.3815T>G (p.Met1272Arg) c.*1656T>G (n.*1656T>G) c.3875T>G (p.Met1292Arg) n.3582T>G c.4127T>G (p.Met1376Arg) c.4028T>G (p.Met1343Arg) c.4442T>G (p.Met1481Arg) | |
16 | g.9763258A>G | CA394705370 | GRIN2A | c.4286T>C (p.Met1429Thr) c.*97T>C (n.*97T>C) n.3536T>C c.3815T>C (p.Met1272Thr) c.*1656T>C (n.*1656T>C) c.3875T>C (p.Met1292Thr) n.3582T>C c.4127T>C (p.Met1376Thr) c.4028T>C (p.Met1343Thr) c.4442T>C (p.Met1481Thr) | gnomAD v4 |
16 | g.9763258A>T | CA394705386 | GRIN2A | c.4286T>A (p.Met1429Lys) c.*97T>A (n.*97T>A) n.3536T>A c.3815T>A (p.Met1272Lys) c.*1656T>A (n.*1656T>A) c.3875T>A (p.Met1292Lys) n.3582T>A c.4127T>A (p.Met1376Lys) c.4028T>A (p.Met1343Lys) c.4442T>A (p.Met1481Lys) | |
16 | g.9763259T>A | CA394705389 | GRIN2A | c.4285A>T (p.Met1429Leu) c.*96A>T (n.*96A>T) n.3535A>T c.3814A>T (p.Met1272Leu) c.*1655A>T (n.*1655A>T) c.3874A>T (p.Met1292Leu) n.3581A>T c.4126A>T (p.Met1376Leu) c.4027A>T (p.Met1343Leu) c.4441A>T (p.Met1481Leu) | dbSNP gnomAD v4 |
16 | g.9763259T>C | CA394705391 | GRIN2A | c.4285A>G (p.Met1429Val) c.*96A>G (n.*96A>G) n.3535A>G c.3814A>G (p.Met1272Val) c.*1655A>G (n.*1655A>G) c.3874A>G (p.Met1292Val) n.3581A>G c.4126A>G (p.Met1376Val) c.4027A>G (p.Met1343Val) c.4441A>G (p.Met1481Val) | |
16 | g.9763259T>G | CA394705393 | GRIN2A | c.4285A>C (p.Met1429Leu) c.*96A>C (n.*96A>C) n.3535A>C c.3814A>C (p.Met1272Leu) c.*1655A>C (n.*1655A>C) c.3874A>C (p.Met1292Leu) n.3581A>C c.4126A>C (p.Met1376Leu) c.4027A>C (p.Met1343Leu) c.4441A>C (p.Met1481Leu) | |
16 | g.9763259T= | CA2206692632 | GRIN2A | c.4285A= (p.Met1429=) c.*96A= (n.*96A=) n.3535A= c.3814A= (p.Met1272=) c.*1655A= (n.*1655A=) c.3874A= (p.Met1292=) n.3581A= c.4126A= (p.Met1376=) c.4027A= (p.Met1343=) c.4441A= (p.Met1481=) | |
16 | g.9763260A>C | CA493692516 | GRIN2A | c.4284T>G (p.Val1428=) c.*95T>G (n.*95T>G) n.3534T>G c.3813T>G (p.Val1271=) c.*1654T>G (n.*1654T>G) c.3873T>G (p.Val1291=) n.3580T>G c.4125T>G (p.Val1375=) c.4026T>G (p.Val1342=) c.4440T>G (p.Val1480=) | |
16 | g.9763260A>G | CA493692517 | GRIN2A | c.4284T>C (p.Val1428=) c.*95T>C (n.*95T>C) n.3534T>C c.3813T>C (p.Val1271=) c.*1654T>C (n.*1654T>C) c.3873T>C (p.Val1291=) n.3580T>C c.4125T>C (p.Val1375=) c.4026T>C (p.Val1342=) c.4440T>C (p.Val1480=) | |
16 | g.9763260A>T | CA493692518 | GRIN2A | c.4284T>A (p.Val1428=) c.*95T>A (n.*95T>A) n.3534T>A c.3813T>A (p.Val1271=) c.*1654T>A (n.*1654T>A) c.3873T>A (p.Val1291=) n.3580T>A c.4125T>A (p.Val1375=) c.4026T>A (p.Val1342=) c.4440T>A (p.Val1480=) | |
16 | g.9763261A= | CA2206692633 | GRIN2A | c.4283T= (p.Val1428=) c.*94T= (n.*94T=) n.3533T= c.3812T= (p.Val1271=) c.*1653T= (n.*1653T=) c.3872T= (p.Val1291=) n.3579T= c.4124T= (p.Val1375=) c.4025T= (p.Val1342=) c.4439T= (p.Val1480=) | |
16 | g.9763261A>C | CA394705395 | GRIN2A | c.4283T>G (p.Val1428Gly) c.*94T>G (n.*94T>G) n.3533T>G c.3812T>G (p.Val1271Gly) c.*1653T>G (n.*1653T>G) c.3872T>G (p.Val1291Gly) n.3579T>G c.4124T>G (p.Val1375Gly) c.4025T>G (p.Val1342Gly) c.4439T>G (p.Val1480Gly) | |
16 | g.9763261A>G | CA394705397 | GRIN2A | c.4283T>C (p.Val1428Ala) c.*94T>C (n.*94T>C) n.3533T>C c.3812T>C (p.Val1271Ala) c.*1653T>C (n.*1653T>C) c.3872T>C (p.Val1291Ala) n.3579T>C c.4124T>C (p.Val1375Ala) c.4025T>C (p.Val1342Ala) c.4439T>C (p.Val1480Ala) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.9763261A>T | CA394705399 | GRIN2A | c.4283T>A (p.Val1428Asp) c.*94T>A (n.*94T>A) n.3533T>A c.3812T>A (p.Val1271Asp) c.*1653T>A (n.*1653T>A) c.3872T>A (p.Val1291Asp) n.3579T>A c.4124T>A (p.Val1375Asp) c.4025T>A (p.Val1342Asp) c.4439T>A (p.Val1480Asp) | |
16 | g.9763262C>A | CA394705400 | GRIN2A | c.4282G>T (p.Val1428Phe) c.*93G>T (n.*93G>T) n.3532G>T c.3811G>T (p.Val1271Phe) c.*1652G>T (n.*1652G>T) c.3871G>T (p.Val1291Phe) n.3578G>T c.4123G>T (p.Val1375Phe) c.4024G>T (p.Val1342Phe) c.4438G>T (p.Val1480Phe) | |
16 | g.9763262C>G | CA394705404 | GRIN2A | c.4282G>C (p.Val1428Leu) c.*93G>C (n.*93G>C) n.3532G>C c.3811G>C (p.Val1271Leu) c.*1652G>C (n.*1652G>C) c.3871G>C (p.Val1291Leu) n.3578G>C c.4123G>C (p.Val1375Leu) c.4024G>C (p.Val1342Leu) c.4438G>C (p.Val1480Leu) | dbSNP |
16 | g.9763262C>T | CA394705402 | GRIN2A | c.4282G>A (p.Val1428Ile) c.*93G>A (n.*93G>A) n.3532G>A c.3811G>A (p.Val1271Ile) c.*1652G>A (n.*1652G>A) c.3871G>A (p.Val1291Ile) n.3578G>A c.4123G>A (p.Val1375Ile) c.4024G>A (p.Val1342Ile) c.4438G>A (p.Val1480Ile) | ClinVar dbSNP gnomAD v4 |
16 | g.9763263A>C | CA394705406 | GRIN2A | c.4281T>G (p.His1427Gln) c.*92T>G (n.*92T>G) n.3531T>G c.3810T>G (p.His1270Gln) c.*1651T>G (n.*1651T>G) c.3870T>G (p.His1290Gln) n.3577T>G c.4122T>G (p.His1374Gln) c.4023T>G (p.His1341Gln) c.4437T>G (p.His1479Gln) | |
16 | g.9763263A>G | CA493692522 | GRIN2A | c.4281T>C (p.His1427=) c.*92T>C (n.*92T>C) n.3531T>C c.3810T>C (p.His1270=) c.*1651T>C (n.*1651T>C) c.3870T>C (p.His1290=) n.3577T>C c.4122T>C (p.His1374=) c.4023T>C (p.His1341=) c.4437T>C (p.His1479=) | |
16 | g.9763263A>T | CA394705408 | GRIN2A | c.4281T>A (p.His1427Gln) c.*92T>A (n.*92T>A) n.3531T>A c.3810T>A (p.His1270Gln) c.*1651T>A (n.*1651T>A) c.3870T>A (p.His1290Gln) n.3577T>A c.4122T>A (p.His1374Gln) c.4023T>A (p.His1341Gln) c.4437T>A (p.His1479Gln) | |
16 | g.9763264T>A | CA394705410 | GRIN2A | c.4280A>T (p.His1427Leu) c.*91A>T (n.*91A>T) n.3530A>T c.3809A>T (p.His1270Leu) c.*1650A>T (n.*1650A>T) c.3869A>T (p.His1290Leu) n.3576A>T c.4121A>T (p.His1374Leu) c.4022A>T (p.His1341Leu) c.4436A>T (p.His1479Leu) | |
16 | g.9763264T>C | CA394705412 | GRIN2A | c.4280A>G (p.His1427Arg) c.*91A>G (n.*91A>G) n.3530A>G c.3809A>G (p.His1270Arg) c.*1650A>G (n.*1650A>G) c.3869A>G (p.His1290Arg) n.3576A>G c.4121A>G (p.His1374Arg) c.4022A>G (p.His1341Arg) c.4436A>G (p.His1479Arg) | |
16 | g.9763264T>G | CA394705415 | GRIN2A | c.4280A>C (p.His1427Pro) c.*91A>C (n.*91A>C) n.3530A>C c.3809A>C (p.His1270Pro) c.*1650A>C (n.*1650A>C) c.3869A>C (p.His1290Pro) n.3576A>C c.4121A>C (p.His1374Pro) c.4022A>C (p.His1341Pro) c.4436A>C (p.His1479Pro) | |
16 | g.9763265G>A | CA394705417 | GRIN2A | c.4279C>T (p.His1427Tyr) c.*90C>T (n.*90C>T) n.3529C>T c.3808C>T (p.His1270Tyr) c.*1649C>T (n.*1649C>T) c.3868C>T (p.His1290Tyr) n.3575C>T c.4120C>T (p.His1374Tyr) c.4021C>T (p.His1341Tyr) c.4435C>T (p.His1479Tyr) | |
16 | g.9763265G>C | CA394705419 | GRIN2A | c.4279C>G (p.His1427Asp) c.*90C>G (n.*90C>G) n.3529C>G c.3808C>G (p.His1270Asp) c.*1649C>G (n.*1649C>G) c.3868C>G (p.His1290Asp) n.3575C>G c.4120C>G (p.His1374Asp) c.4021C>G (p.His1341Asp) c.4435C>G (p.His1479Asp) | |
16 | g.9763265G>T | CA394705420 | GRIN2A | c.4279C>A (p.His1427Asn) c.*90C>A (n.*90C>A) n.3529C>A c.3808C>A (p.His1270Asn) c.*1649C>A (n.*1649C>A) c.3868C>A (p.His1290Asn) n.3575C>A c.4120C>A (p.His1374Asn) c.4021C>A (p.His1341Asn) c.4435C>A (p.His1479Asn) | |
16 | g.9763266C>A | CA394705422 | GRIN2A | c.4278G>T (p.Glu1426Asp) c.*89G>T (n.*89G>T) n.3528G>T c.3807G>T (p.Glu1269Asp) c.*1648G>T (n.*1648G>T) c.3867G>T (p.Glu1289Asp) n.3574G>T c.4119G>T (p.Glu1373Asp) c.4020G>T (p.Glu1340Asp) c.4434G>T (p.Glu1478Asp) | |
16 | g.9763266C>G | CA394705424 | GRIN2A | c.4278G>C (p.Glu1426Asp) c.*89G>C (n.*89G>C) n.3528G>C c.3807G>C (p.Glu1269Asp) c.*1648G>C (n.*1648G>C) c.3867G>C (p.Glu1289Asp) n.3574G>C c.4119G>C (p.Glu1373Asp) c.4020G>C (p.Glu1340Asp) c.4434G>C (p.Glu1478Asp) | gnomAD v4 |
16 | g.9763266C>T | CA493692523 | GRIN2A | c.4278G>A (p.Glu1426=) c.*89G>A (n.*89G>A) n.3528G>A c.3807G>A (p.Glu1269=) c.*1648G>A (n.*1648G>A) c.3867G>A (p.Glu1289=) n.3574G>A c.4119G>A (p.Glu1373=) c.4020G>A (p.Glu1340=) c.4434G>A (p.Glu1478=) | dbSNP |
16 | g.9763267T>A | CA394705429 | GRIN2A | c.4277A>T (p.Glu1426Val) c.*88A>T (n.*88A>T) n.3527A>T c.3806A>T (p.Glu1269Val) c.*1647A>T (n.*1647A>T) c.3866A>T (p.Glu1289Val) n.3573A>T c.4118A>T (p.Glu1373Val) c.4019A>T (p.Glu1340Val) c.4433A>T (p.Glu1478Val) | dbSNP |
16 | g.9763267T>C | CA394705430 | GRIN2A | c.4277A>G (p.Glu1426Gly) c.*88A>G (n.*88A>G) n.3527A>G c.3806A>G (p.Glu1269Gly) c.*1647A>G (n.*1647A>G) c.3866A>G (p.Glu1289Gly) n.3573A>G c.4118A>G (p.Glu1373Gly) c.4019A>G (p.Glu1340Gly) c.4433A>G (p.Glu1478Gly) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
16 | g.9763267T>G | CA394705426 | GRIN2A | c.4277A>C (p.Glu1426Ala) c.*88A>C (n.*88A>C) n.3527A>C c.3806A>C (p.Glu1269Ala) c.*1647A>C (n.*1647A>C) c.3866A>C (p.Glu1289Ala) n.3573A>C c.4118A>C (p.Glu1373Ala) c.4019A>C (p.Glu1340Ala) c.4433A>C (p.Glu1478Ala) | |
16 | g.9763267T= | CA2206692634 | GRIN2A | c.4277A= (p.Glu1426=) c.*88A= (n.*88A=) n.3527A= c.3806A= (p.Glu1269=) c.*1647A= (n.*1647A=) c.3866A= (p.Glu1289=) n.3573A= c.4118A= (p.Glu1373=) c.4019A= (p.Glu1340=) c.4433A= (p.Glu1478=) | |
16 | g.9763268C>A | CA394705434 | GRIN2A | c.4276G>T (p.Glu1426Ter) c.*87G>T (n.*87G>T) n.3526G>T c.3805G>T (p.Glu1269Ter) c.*1646G>T (n.*1646G>T) c.3865G>T (p.Glu1289Ter) n.3572G>T c.4117G>T (p.Glu1373Ter) c.4018G>T (p.Glu1340Ter) c.4432G>T (p.Glu1478Ter) | dbSNP |
16 | g.9763268C= | CA2206692635 | GRIN2A | c.4276G= (p.Glu1426=) c.*87G= (n.*87G=) n.3526G= c.3805G= (p.Glu1269=) c.*1646G= (n.*1646G=) c.3865G= (p.Glu1289=) n.3572G= c.4117G= (p.Glu1373=) c.4018G= (p.Glu1340=) c.4432G= (p.Glu1478=) | |
16 | g.9763268C>G | CA394705436 | GRIN2A | c.4276G>C (p.Glu1426Gln) c.*87G>C (n.*87G>C) n.3526G>C c.3805G>C (p.Glu1269Gln) c.*1646G>C (n.*1646G>C) c.3865G>C (p.Glu1289Gln) n.3572G>C c.4117G>C (p.Glu1373Gln) c.4018G>C (p.Glu1340Gln) c.4432G>C (p.Glu1478Gln) | |
16 | g.9763268C>T | CA277535846 | GRIN2A | c.4276G>A (p.Glu1426Lys) c.*87G>A (n.*87G>A) n.3526G>A c.3805G>A (p.Glu1269Lys) c.*1646G>A (n.*1646G>A) c.3865G>A (p.Glu1289Lys) n.3572G>A c.4117G>A (p.Glu1373Lys) c.4018G>A (p.Glu1340Lys) c.4432G>A (p.Glu1478Lys) | dbSNP COSMIC |
16 | g.9763269C>A | CA493692527 | GRIN2A | c.4275G>T (p.Ser1425=) c.*86G>T (n.*86G>T) n.3525G>T c.3804G>T (p.Ser1268=) c.*1645G>T (n.*1645G>T) c.3864G>T (p.Ser1288=) n.3571G>T c.4116G>T (p.Ser1372=) c.4017G>T (p.Ser1339=) c.4431G>T (p.Ser1477=) | |
16 | g.9763269C= | CA2206692636 | GRIN2A | c.4275G= (p.Ser1425=) c.*86G= (n.*86G=) n.3525G= c.3804G= (p.Ser1268=) c.*1645G= (n.*1645G=) c.3864G= (p.Ser1288=) n.3571G= c.4116G= (p.Ser1372=) c.4017G= (p.Ser1339=) c.4431G= (p.Ser1477=) | |
16 | g.9763269C>G | CA493692526 | GRIN2A | c.4275G>C (p.Ser1425=) c.*86G>C (n.*86G>C) n.3525G>C c.3804G>C (p.Ser1268=) c.*1645G>C (n.*1645G>C) c.3864G>C (p.Ser1288=) n.3571G>C c.4116G>C (p.Ser1372=) c.4017G>C (p.Ser1339=) c.4431G>C (p.Ser1477=) | |
16 | g.9763269C>T | CA7896184 | GRIN2A | c.4275G>A (p.Ser1425=) c.*86G>A (n.*86G>A) n.3525G>A c.3804G>A (p.Ser1268=) c.*1645G>A (n.*1645G>A) c.3864G>A (p.Ser1288=) n.3571G>A c.4116G>A (p.Ser1372=) c.4017G>A (p.Ser1339=) c.4431G>A (p.Ser1477=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.9763270G>A | CA277535861 | GRIN2A | c.4274C>T (p.Ser1425Leu) c.*85C>T (n.*85C>T) n.3524C>T c.3803C>T (p.Ser1268Leu) c.*1644C>T (n.*1644C>T) c.3863C>T (p.Ser1288Leu) n.3570C>T c.4115C>T (p.Ser1372Leu) c.4016C>T (p.Ser1339Leu) c.4430C>T (p.Ser1477Leu) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
16 | g.9763270G>C | CA394705442 | GRIN2A | c.4274C>G (p.Ser1425Trp) c.*85C>G (n.*85C>G) n.3524C>G c.3803C>G (p.Ser1268Trp) c.*1644C>G (n.*1644C>G) c.3863C>G (p.Ser1288Trp) n.3570C>G c.4115C>G (p.Ser1372Trp) c.4016C>G (p.Ser1339Trp) c.4430C>G (p.Ser1477Trp) | |
16 | g.9763270G= | CA2206692637 | GRIN2A | c.4274C= (p.Ser1425=) c.*85C= (n.*85C=) n.3524C= c.3803C= (p.Ser1268=) c.*1644C= (n.*1644C=) c.3863C= (p.Ser1288=) n.3570C= c.4115C= (p.Ser1372=) c.4016C= (p.Ser1339=) c.4430C= (p.Ser1477=) | |
16 | g.9763270G>T | CA394705444 | GRIN2A | c.4274C>A (p.Ser1425Ter) c.*85C>A (n.*85C>A) n.3524C>A c.3803C>A (p.Ser1268Ter) c.*1644C>A (n.*1644C>A) c.3863C>A (p.Ser1288Ter) n.3570C>A c.4115C>A (p.Ser1372Ter) c.4016C>A (p.Ser1339Ter) c.4430C>A (p.Ser1477Ter) | dbSNP |
16 | g.9763271A>C | CA394705447 | GRIN2A | c.4273T>G (p.Ser1425Ala) c.*84T>G (n.*84T>G) n.3523T>G c.3802T>G (p.Ser1268Ala) c.*1643T>G (n.*1643T>G) c.3862T>G (p.Ser1288Ala) n.3569T>G c.4114T>G (p.Ser1372Ala) c.4015T>G (p.Ser1339Ala) c.4429T>G (p.Ser1477Ala) | |
16 | g.9763271A>G | CA394705450 | GRIN2A | c.4273T>C (p.Ser1425Pro) c.*84T>C (n.*84T>C) n.3523T>C c.3802T>C (p.Ser1268Pro) c.*1643T>C (n.*1643T>C) c.3862T>C (p.Ser1288Pro) n.3569T>C c.4114T>C (p.Ser1372Pro) c.4015T>C (p.Ser1339Pro) c.4429T>C (p.Ser1477Pro) | |
16 | g.9763271A>T | CA394705448 | GRIN2A | c.4273T>A (p.Ser1425Thr) c.*84T>A (n.*84T>A) n.3523T>A c.3802T>A (p.Ser1268Thr) c.*1643T>A (n.*1643T>A) c.3862T>A (p.Ser1288Thr) n.3569T>A c.4114T>A (p.Ser1372Thr) c.4015T>A (p.Ser1339Thr) c.4429T>A (p.Ser1477Thr) | |
16 | g.9763272A>C | CA394705452 | GRIN2A | c.4272T>G (p.Ile1424Met) c.*83T>G (n.*83T>G) n.3522T>G c.3801T>G (p.Ile1267Met) c.*1642T>G (n.*1642T>G) c.3861T>G (p.Ile1287Met) n.3568T>G c.4113T>G (p.Ile1371Met) c.4014T>G (p.Ile1338Met) c.4428T>G (p.Ile1476Met) | |
16 | g.9763272A>G | CA493692529 | GRIN2A | c.4272T>C (p.Ile1424=) c.*83T>C (n.*83T>C) n.3522T>C c.3801T>C (p.Ile1267=) c.*1642T>C (n.*1642T>C) c.3861T>C (p.Ile1287=) n.3568T>C c.4113T>C (p.Ile1371=) c.4014T>C (p.Ile1338=) c.4428T>C (p.Ile1476=) | gnomAD v4 |
16 | g.9763272A>T | CA493692530 | GRIN2A | c.4272T>A (p.Ile1424=) c.*83T>A (n.*83T>A) n.3522T>A c.3801T>A (p.Ile1267=) c.*1642T>A (n.*1642T>A) c.3861T>A (p.Ile1287=) n.3568T>A c.4113T>A (p.Ile1371=) c.4014T>A (p.Ile1338=) c.4428T>A (p.Ile1476=) | |
16 | g.9763273A= | CA2206692638 | GRIN2A | c.4271T= (p.Ile1424=) c.*82T= (n.*82T=) n.3521T= c.3800T= (p.Ile1267=) c.*1641T= (n.*1641T=) c.3860T= (p.Ile1287=) n.3567T= c.4112T= (p.Ile1371=) c.4013T= (p.Ile1338=) c.4427T= (p.Ile1476=) | |
16 | g.9763273A>C | CA394705454 | GRIN2A | c.4271T>G (p.Ile1424Ser) c.*82T>G (n.*82T>G) n.3521T>G c.3800T>G (p.Ile1267Ser) c.*1641T>G (n.*1641T>G) c.3860T>G (p.Ile1287Ser) n.3567T>G c.4112T>G (p.Ile1371Ser) c.4013T>G (p.Ile1338Ser) c.4427T>G (p.Ile1476Ser) | |
16 | g.9763273A>G | CA394705456 | GRIN2A | c.4271T>C (p.Ile1424Thr) c.*82T>C (n.*82T>C) n.3521T>C c.3800T>C (p.Ile1267Thr) c.*1641T>C (n.*1641T>C) c.3860T>C (p.Ile1287Thr) n.3567T>C c.4112T>C (p.Ile1371Thr) c.4013T>C (p.Ile1338Thr) c.4427T>C (p.Ile1476Thr) | ClinVar dbSNP |
16 | g.9763273A>T | CA394705458 | GRIN2A | c.4271T>A (p.Ile1424Asn) c.*82T>A (n.*82T>A) n.3521T>A c.3800T>A (p.Ile1267Asn) c.*1641T>A (n.*1641T>A) c.3860T>A (p.Ile1287Asn) n.3567T>A c.4112T>A (p.Ile1371Asn) c.4013T>A (p.Ile1338Asn) c.4427T>A (p.Ile1476Asn) | |
16 | g.9763274T>A | CA394705461 | GRIN2A | c.4270A>T (p.Ile1424Phe) c.*81A>T (n.*81A>T) n.3520A>T c.3799A>T (p.Ile1267Phe) c.*1640A>T (n.*1640A>T) c.3859A>T (p.Ile1287Phe) n.3566A>T c.4111A>T (p.Ile1371Phe) c.4012A>T (p.Ile1338Phe) c.4426A>T (p.Ile1476Phe) | |
16 | g.9763274T>C | CA394705465 | GRIN2A | c.4270A>G (p.Ile1424Val) c.*81A>G (n.*81A>G) n.3520A>G c.3799A>G (p.Ile1267Val) c.*1640A>G (n.*1640A>G) c.3859A>G (p.Ile1287Val) n.3566A>G c.4111A>G (p.Ile1371Val) c.4012A>G (p.Ile1338Val) c.4426A>G (p.Ile1476Val) | |
16 | g.9763274T>G | CA394705463 | GRIN2A | c.4270A>C (p.Ile1424Leu) c.*81A>C (n.*81A>C) n.3520A>C c.3799A>C (p.Ile1267Leu) c.*1640A>C (n.*1640A>C) c.3859A>C (p.Ile1287Leu) n.3566A>C c.4111A>C (p.Ile1371Leu) c.4012A>C (p.Ile1338Leu) c.4426A>C (p.Ile1476Leu) | |
16 | g.9763275A= | CA2206692639 | GRIN2A | c.4269T= (p.Tyr1423=) c.*80T= (n.*80T=) n.3519T= c.3798T= (p.Tyr1266=) c.*1639T= (n.*1639T=) c.3858T= (p.Tyr1286=) n.3565T= c.4110T= (p.Tyr1370=) c.4011T= (p.Tyr1337=) c.4425T= (p.Tyr1475=) | |
16 | g.9763275A>C | CA394705466 | GRIN2A | c.4269T>G (p.Tyr1423Ter) c.*80T>G (n.*80T>G) n.3519T>G c.3798T>G (p.Tyr1266Ter) c.*1639T>G (n.*1639T>G) c.3858T>G (p.Tyr1286Ter) n.3565T>G c.4110T>G (p.Tyr1370Ter) c.4011T>G (p.Tyr1337Ter) c.4425T>G (p.Tyr1475Ter) | |
16 | g.9763275A>G | CA7896185 | GRIN2A | c.4269T>C (p.Tyr1423=) c.*80T>C (n.*80T>C) n.3519T>C c.3798T>C (p.Tyr1266=) c.*1639T>C (n.*1639T>C) c.3858T>C (p.Tyr1286=) n.3565T>C c.4110T>C (p.Tyr1370=) c.4011T>C (p.Tyr1337=) c.4425T>C (p.Tyr1475=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.9763275A>T | CA394705468 | GRIN2A | c.4269T>A (p.Tyr1423Ter) c.*80T>A (n.*80T>A) n.3519T>A c.3798T>A (p.Tyr1266Ter) c.*1639T>A (n.*1639T>A) c.3858T>A (p.Tyr1286Ter) n.3565T>A c.4110T>A (p.Tyr1370Ter) c.4011T>A (p.Tyr1337Ter) c.4425T>A (p.Tyr1475Ter) | |
16 | g.9763276T>A | CA394705471 | GRIN2A | c.4268A>T (p.Tyr1423Phe) c.*79A>T (n.*79A>T) n.3518A>T c.3797A>T (p.Tyr1266Phe) c.*1638A>T (n.*1638A>T) c.3857A>T (p.Tyr1286Phe) n.3564A>T c.4109A>T (p.Tyr1370Phe) c.4010A>T (p.Tyr1337Phe) c.4424A>T (p.Tyr1475Phe) | |
16 | g.9763276T>C | CA394705474 | GRIN2A | c.4268A>G (p.Tyr1423Cys) c.*79A>G (n.*79A>G) n.3518A>G c.3797A>G (p.Tyr1266Cys) c.*1638A>G (n.*1638A>G) c.3857A>G (p.Tyr1286Cys) n.3564A>G c.4109A>G (p.Tyr1370Cys) c.4010A>G (p.Tyr1337Cys) c.4424A>G (p.Tyr1475Cys) | |
16 | g.9763276T>G | CA394705476 | GRIN2A | c.4268A>C (p.Tyr1423Ser) c.*79A>C (n.*79A>C) n.3518A>C c.3797A>C (p.Tyr1266Ser) c.*1638A>C (n.*1638A>C) c.3857A>C (p.Tyr1286Ser) n.3564A>C c.4109A>C (p.Tyr1370Ser) c.4010A>C (p.Tyr1337Ser) c.4424A>C (p.Tyr1475Ser) | |
16 | g.9763277A= | CA2206692640 | GRIN2A | c.4267T= (p.Tyr1423=) c.*78T= (n.*78T=) n.3517T= c.3796T= (p.Tyr1266=) c.*1637T= (n.*1637T=) c.3856T= (p.Tyr1286=) n.3563T= c.4108T= (p.Tyr1370=) c.4009T= (p.Tyr1337=) c.4423T= (p.Tyr1475=) | |
16 | g.9763277A>C | CA394705479 | GRIN2A | c.4267T>G (p.Tyr1423Asp) c.*78T>G (n.*78T>G) n.3517T>G c.3796T>G (p.Tyr1266Asp) c.*1637T>G (n.*1637T>G) c.3856T>G (p.Tyr1286Asp) n.3563T>G c.4108T>G (p.Tyr1370Asp) c.4009T>G (p.Tyr1337Asp) c.4423T>G (p.Tyr1475Asp) | ClinVar dbSNP |
16 | g.9763277A>G | CA394705481 | GRIN2A | c.4267T>C (p.Tyr1423His) c.*78T>C (n.*78T>C) n.3517T>C c.3796T>C (p.Tyr1266His) c.*1637T>C (n.*1637T>C) c.3856T>C (p.Tyr1286His) n.3563T>C c.4108T>C (p.Tyr1370His) c.4009T>C (p.Tyr1337His) c.4423T>C (p.Tyr1475His) | |
16 | g.9763277A>T | CA394705483 | GRIN2A | c.4267T>A (p.Tyr1423Asn) c.*78T>A (n.*78T>A) n.3517T>A c.3796T>A (p.Tyr1266Asn) c.*1637T>A (n.*1637T>A) c.3856T>A (p.Tyr1286Asn) n.3563T>A c.4108T>A (p.Tyr1370Asn) c.4009T>A (p.Tyr1337Asn) c.4423T>A (p.Tyr1475Asn) | |
16 | g.9763278C>A | CA493692535 | GRIN2A | c.4266G>T (p.Val1422=) c.*77G>T (n.*77G>T) n.3516G>T c.3795G>T (p.Val1265=) c.*1636G>T (n.*1636G>T) c.3855G>T (p.Val1285=) n.3562G>T c.4107G>T (p.Val1369=) c.4008G>T (p.Val1336=) c.4422G>T (p.Val1474=) | dbSNP |
16 | g.9763278C= | CA2206692641 | GRIN2A | c.4266G= (p.Val1422=) c.*77G= (n.*77G=) n.3516G= c.3795G= (p.Val1265=) c.*1636G= (n.*1636G=) c.3855G= (p.Val1285=) n.3562G= c.4107G= (p.Val1369=) c.4008G= (p.Val1336=) c.4422G= (p.Val1474=) | |
16 | g.9763278C>G | CA493692536 | GRIN2A | c.4266G>C (p.Val1422=) c.*77G>C (n.*77G>C) n.3516G>C c.3795G>C (p.Val1265=) c.*1636G>C (n.*1636G>C) c.3855G>C (p.Val1285=) n.3562G>C c.4107G>C (p.Val1369=) c.4008G>C (p.Val1336=) c.4422G>C (p.Val1474=) | |
16 | g.9763278C>T | CA493692537 | GRIN2A | c.4266G>A (p.Val1422=) c.*77G>A (n.*77G>A) n.3516G>A c.3795G>A (p.Val1265=) c.*1636G>A (n.*1636G>A) c.3855G>A (p.Val1285=) n.3562G>A c.4107G>A (p.Val1369=) c.4008G>A (p.Val1336=) c.4422G>A (p.Val1474=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
16 | g.9763279A>C | CA394705486 | GRIN2A | c.4265T>G (p.Val1422Gly) c.*76T>G (n.*76T>G) n.3515T>G c.3794T>G (p.Val1265Gly) c.*1635T>G (n.*1635T>G) c.3854T>G (p.Val1285Gly) n.3561T>G c.4106T>G (p.Val1369Gly) c.4007T>G (p.Val1336Gly) c.4421T>G (p.Val1474Gly) | |
16 | g.9763279A>G | CA394705487 | GRIN2A | c.4265T>C (p.Val1422Ala) c.*76T>C (n.*76T>C) n.3515T>C c.3794T>C (p.Val1265Ala) c.*1635T>C (n.*1635T>C) c.3854T>C (p.Val1285Ala) n.3561T>C c.4106T>C (p.Val1369Ala) c.4007T>C (p.Val1336Ala) c.4421T>C (p.Val1474Ala) | |
16 | g.9763279A>T | CA394705489 | GRIN2A | c.4265T>A (p.Val1422Glu) c.*76T>A (n.*76T>A) n.3515T>A c.3794T>A (p.Val1265Glu) c.*1635T>A (n.*1635T>A) c.3854T>A (p.Val1285Glu) n.3561T>A c.4106T>A (p.Val1369Glu) c.4007T>A (p.Val1336Glu) c.4421T>A (p.Val1474Glu) | |
16 | g.9763280C>A | CA394705492 | GRIN2A | c.4264G>T (p.Val1422Leu) c.*75G>T (n.*75G>T) n.3514G>T c.3793G>T (p.Val1265Leu) c.*1634G>T (n.*1634G>T) c.3853G>T (p.Val1285Leu) n.3560G>T c.4105G>T (p.Val1369Leu) c.4006G>T (p.Val1336Leu) c.4420G>T (p.Val1474Leu) | dbSNP |
16 | g.9763280C>G | CA394705495 | GRIN2A | c.4264G>C (p.Val1422Leu) c.*75G>C (n.*75G>C) n.3514G>C c.3793G>C (p.Val1265Leu) c.*1634G>C (n.*1634G>C) c.3853G>C (p.Val1285Leu) n.3560G>C c.4105G>C (p.Val1369Leu) c.4006G>C (p.Val1336Leu) c.4420G>C (p.Val1474Leu) | |
16 | g.9763280C>T | CA394705493 | GRIN2A | c.4264G>A (p.Val1422Met) c.*75G>A (n.*75G>A) n.3514G>A c.3793G>A (p.Val1265Met) c.*1634G>A (n.*1634G>A) c.3853G>A (p.Val1285Met) n.3560G>A c.4105G>A (p.Val1369Met) c.4006G>A (p.Val1336Met) c.4420G>A (p.Val1474Met) | gnomAD v4 |
16 | g.9763281A= | CA2206692642 | GRIN2A | c.4263T= (p.Asp1421=) c.*74T= (n.*74T=) n.3513T= c.3792T= (p.Asp1264=) c.*1633T= (n.*1633T=) c.3852T= (p.Asp1284=) n.3559T= c.4104T= (p.Asp1368=) c.4005T= (p.Asp1335=) c.4419T= (p.Asp1473=) | |
16 | g.9763281A>C | CA394705498 | GRIN2A | c.4263T>G (p.Asp1421Glu) c.*74T>G (n.*74T>G) n.3513T>G c.3792T>G (p.Asp1264Glu) c.*1633T>G (n.*1633T>G) c.3852T>G (p.Asp1284Glu) n.3559T>G c.4104T>G (p.Asp1368Glu) c.4005T>G (p.Asp1335Glu) c.4419T>G (p.Asp1473Glu) | |
16 | g.9763281A>G | CA493692542 | GRIN2A | c.4263T>C (p.Asp1421=) c.*74T>C (n.*74T>C) n.3513T>C c.3792T>C (p.Asp1264=) c.*1633T>C (n.*1633T>C) c.3852T>C (p.Asp1284=) n.3559T>C c.4104T>C (p.Asp1368=) c.4005T>C (p.Asp1335=) c.4419T>C (p.Asp1473=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.9763281A>T | CA394705499 | GRIN2A | c.4263T>A (p.Asp1421Glu) c.*74T>A (n.*74T>A) n.3513T>A c.3792T>A (p.Asp1264Glu) c.*1633T>A (n.*1633T>A) c.3852T>A (p.Asp1284Glu) n.3559T>A c.4104T>A (p.Asp1368Glu) c.4005T>A (p.Asp1335Glu) c.4419T>A (p.Asp1473Glu) | |
16 | g.9763282T>A | CA394705502 | GRIN2A | c.4262A>T (p.Asp1421Val) c.*73A>T (n.*73A>T) n.3512A>T c.3791A>T (p.Asp1264Val) c.*1632A>T (n.*1632A>T) c.3851A>T (p.Asp1284Val) n.3558A>T c.4103A>T (p.Asp1368Val) c.4004A>T (p.Asp1335Val) c.4418A>T (p.Asp1473Val) | ClinVar |
16 | g.9763282T>C | CA394705505 | GRIN2A | c.4262A>G (p.Asp1421Gly) c.*73A>G (n.*73A>G) n.3512A>G c.3791A>G (p.Asp1264Gly) c.*1632A>G (n.*1632A>G) c.3851A>G (p.Asp1284Gly) n.3558A>G c.4103A>G (p.Asp1368Gly) c.4004A>G (p.Asp1335Gly) c.4418A>G (p.Asp1473Gly) | |
16 | g.9763282T>G | CA394705504 | GRIN2A | c.4262A>C (p.Asp1421Ala) c.*73A>C (n.*73A>C) n.3512A>C c.3791A>C (p.Asp1264Ala) c.*1632A>C (n.*1632A>C) c.3851A>C (p.Asp1284Ala) n.3558A>C c.4103A>C (p.Asp1368Ala) c.4004A>C (p.Asp1335Ala) c.4418A>C (p.Asp1473Ala) | |
16 | g.9763283C>A | CA394705509 | GRIN2A | c.4261G>T (p.Asp1421Tyr) c.*72G>T (n.*72G>T) n.3511G>T c.3790G>T (p.Asp1264Tyr) c.*1631G>T (n.*1631G>T) c.3850G>T (p.Asp1284Tyr) n.3557G>T c.4102G>T (p.Asp1368Tyr) c.4003G>T (p.Asp1335Tyr) c.4417G>T (p.Asp1473Tyr) | ClinVar dbSNP |
16 | g.9763283C= | CA2206692643 | GRIN2A | c.4261G= (p.Asp1421=) c.*72G= (n.*72G=) n.3511G= c.3790G= (p.Asp1264=) c.*1631G= (n.*1631G=) c.3850G= (p.Asp1284=) n.3557G= c.4102G= (p.Asp1368=) c.4003G= (p.Asp1335=) c.4417G= (p.Asp1473=) | |
16 | g.9763283C>G | CA394705510 | GRIN2A | c.4261G>C (p.Asp1421His) c.*72G>C (n.*72G>C) n.3511G>C c.3790G>C (p.Asp1264His) c.*1631G>C (n.*1631G>C) c.3850G>C (p.Asp1284His) n.3557G>C c.4102G>C (p.Asp1368His) c.4003G>C (p.Asp1335His) c.4417G>C (p.Asp1473His) | dbSNP |
16 | g.9763283C>T | CA394705512 | GRIN2A | c.4261G>A (p.Asp1421Asn) c.*72G>A (n.*72G>A) n.3511G>A c.3790G>A (p.Asp1264Asn) c.*1631G>A (n.*1631G>A) c.3850G>A (p.Asp1284Asn) n.3557G>A c.4102G>A (p.Asp1368Asn) c.4003G>A (p.Asp1335Asn) c.4417G>A (p.Asp1473Asn) | COSMIC |
16 | g.9763284A= | CA2206692644 | GRIN2A | c.4260T= (p.Asn1420=) c.*71T= (n.*71T=) n.3510T= c.3789T= (p.Asn1263=) c.*1630T= (n.*1630T=) c.3849T= (p.Asn1283=) n.3556T= c.4101T= (p.Asn1367=) c.4002T= (p.Asn1334=) c.4416T= (p.Asn1472=) | |
16 | g.9763284A>C | CA7896186 | GRIN2A | c.4260T>G (p.Asn1420Lys) c.*71T>G (n.*71T>G) n.3510T>G c.3789T>G (p.Asn1263Lys) c.*1630T>G (n.*1630T>G) c.3849T>G (p.Asn1283Lys) n.3556T>G c.4101T>G (p.Asn1367Lys) c.4002T>G (p.Asn1334Lys) c.4416T>G (p.Asn1472Lys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.9763284A>G | CA493692543 | GRIN2A | c.4260T>C (p.Asn1420=) c.*71T>C (n.*71T>C) n.3510T>C c.3789T>C (p.Asn1263=) c.*1630T>C (n.*1630T>C) c.3849T>C (p.Asn1283=) n.3556T>C c.4101T>C (p.Asn1367=) c.4002T>C (p.Asn1334=) c.4416T>C (p.Asn1472=) | |
16 | g.9763284A>T | CA394705515 | GRIN2A | c.4260T>A (p.Asn1420Lys) c.*71T>A (n.*71T>A) n.3510T>A c.3789T>A (p.Asn1263Lys) c.*1630T>A (n.*1630T>A) c.3849T>A (p.Asn1283Lys) n.3556T>A c.4101T>A (p.Asn1367Lys) c.4002T>A (p.Asn1334Lys) c.4416T>A (p.Asn1472Lys) | |
16 | g.9763285T>A | CA394705518 | GRIN2A | c.4259A>T (p.Asn1420Ile) c.*70A>T (n.*70A>T) n.3509A>T c.3788A>T (p.Asn1263Ile) c.*1629A>T (n.*1629A>T) c.3848A>T (p.Asn1283Ile) n.3555A>T c.4100A>T (p.Asn1367Ile) c.4001A>T (p.Asn1334Ile) c.4415A>T (p.Asn1472Ile) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.9763285T>C | CA7896187 | GRIN2A | c.4259A>G (p.Asn1420Ser) c.*70A>G (n.*70A>G) n.3509A>G c.3788A>G (p.Asn1263Ser) c.*1629A>G (n.*1629A>G) c.3848A>G (p.Asn1283Ser) n.3555A>G c.4100A>G (p.Asn1367Ser) c.4001A>G (p.Asn1334Ser) c.4415A>G (p.Asn1472Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.9763285T>G | CA394705521 | GRIN2A | c.4259A>C (p.Asn1420Thr) c.*70A>C (n.*70A>C) n.3509A>C c.3788A>C (p.Asn1263Thr) c.*1629A>C (n.*1629A>C) c.3848A>C (p.Asn1283Thr) n.3555A>C c.4100A>C (p.Asn1367Thr) c.4001A>C (p.Asn1334Thr) c.4415A>C (p.Asn1472Thr) | |
16 | g.9763285T= | CA2206692645 | GRIN2A | c.4259A= (p.Asn1420=) c.*70A= (n.*70A=) n.3509A= c.3788A= (p.Asn1263=) c.*1629A= (n.*1629A=) c.3848A= (p.Asn1283=) n.3555A= c.4100A= (p.Asn1367=) c.4001A= (p.Asn1334=) c.4415A= (p.Asn1472=) | |
16 | g.9763286T>A | CA394705525 | GRIN2A | c.4258A>T (p.Asn1420Tyr) c.*69A>T (n.*69A>T) n.3508A>T c.3787A>T (p.Asn1263Tyr) c.*1628A>T (n.*1628A>T) c.3847A>T (p.Asn1283Tyr) n.3554A>T c.4099A>T (p.Asn1367Tyr) c.4000A>T (p.Asn1334Tyr) c.4414A>T (p.Asn1472Tyr) | |
16 | g.9763286T>C | CA394705526 | GRIN2A | c.4258A>G (p.Asn1420Asp) c.*69A>G (n.*69A>G) n.3508A>G c.3787A>G (p.Asn1263Asp) c.*1628A>G (n.*1628A>G) c.3847A>G (p.Asn1283Asp) n.3554A>G c.4099A>G (p.Asn1367Asp) c.4000A>G (p.Asn1334Asp) c.4414A>G (p.Asn1472Asp) | |
16 | g.9763286T>G | CA394705528 | GRIN2A | c.4258A>C (p.Asn1420His) c.*69A>C (n.*69A>C) n.3508A>C c.3787A>C (p.Asn1263His) c.*1628A>C (n.*1628A>C) c.3847A>C (p.Asn1283His) n.3554A>C c.4099A>C (p.Asn1367His) c.4000A>C (p.Asn1334His) c.4414A>C (p.Asn1472His) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.9763286T= | CA2206692646 | GRIN2A | c.4258A= (p.Asn1420=) c.*69A= (n.*69A=) n.3508A= c.3787A= (p.Asn1263=) c.*1628A= (n.*1628A=) c.3847A= (p.Asn1283=) n.3554A= c.4099A= (p.Asn1367=) c.4000A= (p.Asn1334=) c.4414A= (p.Asn1472=) | |
16 | g.9763287G>A | CA493692545 | GRIN2A | c.4257C>T (p.His1419=) c.*68C>T (n.*68C>T) n.3507C>T c.3786C>T (p.His1262=) c.*1627C>T (n.*1627C>T) c.3846C>T (p.His1282=) n.3553C>T c.4098C>T (p.His1366=) c.3999C>T (p.His1333=) c.4413C>T (p.His1471=) | |
16 | g.9763287G>C | CA394705532 | GRIN2A | c.4257C>G (p.His1419Gln) c.*68C>G (n.*68C>G) n.3507C>G c.3786C>G (p.His1262Gln) c.*1627C>G (n.*1627C>G) c.3846C>G (p.His1282Gln) n.3553C>G c.4098C>G (p.His1366Gln) c.3999C>G (p.His1333Gln) c.4413C>G (p.His1471Gln) | |
16 | g.9763287G= | CA2206692647 | GRIN2A | c.4257C= (p.His1419=) c.*68C= (n.*68C=) n.3507C= c.3786C= (p.His1262=) c.*1627C= (n.*1627C=) c.3846C= (p.His1282=) n.3553C= c.4098C= (p.His1366=) c.3999C= (p.His1333=) c.4413C= (p.His1471=) | |
16 | g.9763287G>T | CA394705530 | GRIN2A | c.4257C>A (p.His1419Gln) c.*68C>A (n.*68C>A) n.3507C>A c.3786C>A (p.His1262Gln) c.*1627C>A (n.*1627C>A) c.3846C>A (p.His1282Gln) n.3553C>A c.4098C>A (p.His1366Gln) c.3999C>A (p.His1333Gln) c.4413C>A (p.His1471Gln) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.9763288T>A | CA394705534 | GRIN2A | c.4256A>T (p.His1419Leu) c.*67A>T (n.*67A>T) n.3506A>T c.3785A>T (p.His1262Leu) c.*1626A>T (n.*1626A>T) c.3845A>T (p.His1282Leu) n.3552A>T c.4097A>T (p.His1366Leu) c.3998A>T (p.His1333Leu) c.4412A>T (p.His1471Leu) | |
16 | g.9763288T>C | CA394705536 | GRIN2A | c.4256A>G (p.His1419Arg) c.*67A>G (n.*67A>G) n.3506A>G c.3785A>G (p.His1262Arg) c.*1626A>G (n.*1626A>G) c.3845A>G (p.His1282Arg) n.3552A>G c.4097A>G (p.His1366Arg) c.3998A>G (p.His1333Arg) c.4412A>G (p.His1471Arg) | |
16 | g.9763288T>G | CA394705537 | GRIN2A | c.4256A>C (p.His1419Pro) c.*67A>C (n.*67A>C) n.3506A>C c.3785A>C (p.His1262Pro) c.*1626A>C (n.*1626A>C) c.3845A>C (p.His1282Pro) n.3552A>C c.4097A>C (p.His1366Pro) c.3998A>C (p.His1333Pro) c.4412A>C (p.His1471Pro) | |
16 | g.9763289G>A | CA394705539 | GRIN2A | c.4255C>T (p.His1419Tyr) c.*66C>T (n.*66C>T) n.3505C>T c.3784C>T (p.His1262Tyr) c.*1625C>T (n.*1625C>T) c.3844C>T (p.His1282Tyr) n.3551C>T c.4096C>T (p.His1366Tyr) c.3997C>T (p.His1333Tyr) c.4411C>T (p.His1471Tyr) | dbSNP |
16 | g.9763289G>C | CA394705541 | GRIN2A | c.4255C>G (p.His1419Asp) c.*66C>G (n.*66C>G) n.3505C>G c.3784C>G (p.His1262Asp) c.*1625C>G (n.*1625C>G) c.3844C>G (p.His1282Asp) n.3551C>G c.4096C>G (p.His1366Asp) c.3997C>G (p.His1333Asp) c.4411C>G (p.His1471Asp) | dbSNP |
16 | g.9763289G>T | CA394705552 | GRIN2A | c.4255C>A (p.His1419Asn) c.*66C>A (n.*66C>A) n.3505C>A c.3784C>A (p.His1262Asn) c.*1625C>A (n.*1625C>A) c.3844C>A (p.His1282Asn) n.3551C>A c.4096C>A (p.His1366Asn) c.3997C>A (p.His1333Asn) c.4411C>A (p.His1471Asn) | |
16 | g.9763290G>A | CA493692548 | GRIN2A | c.4254C>T (p.Gly1418=) c.*65C>T (n.*65C>T) n.3504C>T c.3783C>T (p.Gly1261=) c.*1624C>T (n.*1624C>T) c.3843C>T (p.Gly1281=) n.3550C>T c.4095C>T (p.Gly1365=) c.3996C>T (p.Gly1332=) c.4410C>T (p.Gly1470=) | gnomAD v4 |
16 | g.9763290G>C | CA493692549 | GRIN2A | c.4254C>G (p.Gly1418=) c.*65C>G (n.*65C>G) n.3504C>G c.3783C>G (p.Gly1261=) c.*1624C>G (n.*1624C>G) c.3843C>G (p.Gly1281=) n.3550C>G c.4095C>G (p.Gly1365=) c.3996C>G (p.Gly1332=) c.4410C>G (p.Gly1470=) | |
16 | g.9763290G>T | CA493692550 | GRIN2A | c.4254C>A (p.Gly1418=) c.*65C>A (n.*65C>A) n.3504C>A c.3783C>A (p.Gly1261=) c.*1624C>A (n.*1624C>A) c.3843C>A (p.Gly1281=) n.3550C>A c.4095C>A (p.Gly1365=) c.3996C>A (p.Gly1332=) c.4410C>A (p.Gly1470=) | |
16 | g.9763291C>A | CA394705556 | GRIN2A | c.4253G>T (p.Gly1418Val) c.*64G>T (n.*64G>T) n.3503G>T c.3782G>T (p.Gly1261Val) c.*1623G>T (n.*1623G>T) c.3842G>T (p.Gly1281Val) n.3549G>T c.4094G>T (p.Gly1365Val) c.3995G>T (p.Gly1332Val) c.4409G>T (p.Gly1470Val) | dbSNP |
16 | g.9763291C= | CA2206692648 | GRIN2A | c.4253G= (p.Gly1418=) c.*64G= (n.*64G=) n.3503G= c.3782G= (p.Gly1261=) c.*1623G= (n.*1623G=) c.3842G= (p.Gly1281=) n.3549G= c.4094G= (p.Gly1365=) c.3995G= (p.Gly1332=) c.4409G= (p.Gly1470=) | |
16 | g.9763291C>G | CA394705557 | GRIN2A | c.4253G>C (p.Gly1418Ala) c.*64G>C (n.*64G>C) n.3503G>C c.3782G>C (p.Gly1261Ala) c.*1623G>C (n.*1623G>C) c.3842G>C (p.Gly1281Ala) n.3549G>C c.4094G>C (p.Gly1365Ala) c.3995G>C (p.Gly1332Ala) c.4409G>C (p.Gly1470Ala) | |
16 | g.9763291C>T | CA394705558 | GRIN2A | c.4253G>A (p.Gly1418Asp) c.*64G>A (n.*64G>A) n.3503G>A c.3782G>A (p.Gly1261Asp) c.*1623G>A (n.*1623G>A) c.3842G>A (p.Gly1281Asp) n.3549G>A c.4094G>A (p.Gly1365Asp) c.3995G>A (p.Gly1332Asp) c.4409G>A (p.Gly1470Asp) | dbSNP gnomAD v4 |
16 | g.9763292C>A | CA394705560 | GRIN2A | c.4252G>T (p.Gly1418Cys) c.*63G>T (n.*63G>T) n.3502G>T c.3781G>T (p.Gly1261Cys) c.*1622G>T (n.*1622G>T) c.3841G>T (p.Gly1281Cys) n.3548G>T c.4093G>T (p.Gly1365Cys) c.3994G>T (p.Gly1332Cys) c.4408G>T (p.Gly1470Cys) | ClinVar dbSNP |
16 | g.9763292C>G | CA394705562 | GRIN2A | c.4252G>C (p.Gly1418Arg) c.*63G>C (n.*63G>C) n.3502G>C c.3781G>C (p.Gly1261Arg) c.*1622G>C (n.*1622G>C) c.3841G>C (p.Gly1281Arg) n.3548G>C c.4093G>C (p.Gly1365Arg) c.3994G>C (p.Gly1332Arg) c.4408G>C (p.Gly1470Arg) | |
16 | g.9763292C>T | CA394705564 | GRIN2A | c.4252G>A (p.Gly1418Ser) c.*63G>A (n.*63G>A) n.3502G>A c.3781G>A (p.Gly1261Ser) c.*1622G>A (n.*1622G>A) c.3841G>A (p.Gly1281Ser) n.3548G>A c.4093G>A (p.Gly1365Ser) c.3994G>A (p.Gly1332Ser) c.4408G>A (p.Gly1470Ser) | dbSNP |
16 | g.9763293C>A | CA493692551 | GRIN2A | c.4251G>T (p.Arg1417=) c.*62G>T (n.*62G>T) n.3501G>T c.3780G>T (p.Arg1260=) c.*1621G>T (n.*1621G>T) c.3840G>T (p.Arg1280=) n.3547G>T c.4092G>T (p.Arg1364=) c.3993G>T (p.Arg1331=) c.4407G>T (p.Arg1469=) | |
16 | g.9763293C>G | CA493692552 | GRIN2A | c.4251G>C (p.Arg1417=) c.*62G>C (n.*62G>C) n.3501G>C c.3780G>C (p.Arg1260=) c.*1621G>C (n.*1621G>C) c.3840G>C (p.Arg1280=) n.3547G>C c.4092G>C (p.Arg1364=) c.3993G>C (p.Arg1331=) c.4407G>C (p.Arg1469=) | |
16 | g.9763293C>T | CA493692553 | GRIN2A | c.4251G>A (p.Arg1417=) c.*62G>A (n.*62G>A) n.3501G>A c.3780G>A (p.Arg1260=) c.*1621G>A (n.*1621G>A) c.3840G>A (p.Arg1280=) n.3547G>A c.4092G>A (p.Arg1364=) c.3993G>A (p.Arg1331=) c.4407G>A (p.Arg1469=) | dbSNP gnomAD v4 |
16 | g.9763294C>A | CA394705569 | GRIN2A | c.4250G>T (p.Arg1417Leu) c.*61G>T (n.*61G>T) n.3500G>T c.3779G>T (p.Arg1260Leu) c.*1620G>T (n.*1620G>T) c.3839G>T (p.Arg1280Leu) n.3546G>T c.4091G>T (p.Arg1364Leu) c.3992G>T (p.Arg1331Leu) c.4406G>T (p.Arg1469Leu) | dbSNP |
16 | g.9763294C= | CA2206692649 | GRIN2A | c.4250G= (p.Arg1417=) c.*61G= (n.*61G=) n.3500G= c.3779G= (p.Arg1260=) c.*1620G= (n.*1620G=) c.3839G= (p.Arg1280=) n.3546G= c.4091G= (p.Arg1364=) c.3992G= (p.Arg1331=) c.4406G= (p.Arg1469=) | |
16 | g.9763294C>G | CA394705570 | GRIN2A | c.4250G>C (p.Arg1417Pro) c.*61G>C (n.*61G>C) n.3500G>C c.3779G>C (p.Arg1260Pro) c.*1620G>C (n.*1620G>C) c.3839G>C (p.Arg1280Pro) n.3546G>C c.4091G>C (p.Arg1364Pro) c.3992G>C (p.Arg1331Pro) c.4406G>C (p.Arg1469Pro) | |
16 | g.9763294C>T | CA394705567 | GRIN2A | c.4250G>A (p.Arg1417Gln) c.*61G>A (n.*61G>A) n.3500G>A c.3779G>A (p.Arg1260Gln) c.*1620G>A (n.*1620G>A) c.3839G>A (p.Arg1280Gln) n.3546G>A c.4091G>A (p.Arg1364Gln) c.3992G>A (p.Arg1331Gln) c.4406G>A (p.Arg1469Gln) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
16 | g.9763295G>A | CA7896188 | GRIN2A | c.4249C>T (p.Arg1417Trp) c.*60C>T (n.*60C>T) n.3499C>T c.3778C>T (p.Arg1260Trp) c.*1619C>T (n.*1619C>T) c.3838C>T (p.Arg1280Trp) n.3545C>T c.4090C>T (p.Arg1364Trp) c.3991C>T (p.Arg1331Trp) c.4405C>T (p.Arg1469Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.9763295G>C | CA394705575 | GRIN2A | c.4249C>G (p.Arg1417Gly) c.*60C>G (n.*60C>G) n.3499C>G c.3778C>G (p.Arg1260Gly) c.*1619C>G (n.*1619C>G) c.3838C>G (p.Arg1280Gly) n.3545C>G c.4090C>G (p.Arg1364Gly) c.3991C>G (p.Arg1331Gly) c.4405C>G (p.Arg1469Gly) | dbSNP |
16 | g.9763295G= | CA2206692650 | GRIN2A | c.4249C= (p.Arg1417=) c.*60C= (n.*60C=) n.3499C= c.3778C= (p.Arg1260=) c.*1619C= (n.*1619C=) c.3838C= (p.Arg1280=) n.3545C= c.4090C= (p.Arg1364=) c.3991C= (p.Arg1331=) c.4405C= (p.Arg1469=) | |
16 | g.9763295G>T | CA493692554 | GRIN2A | c.4249C>A (p.Arg1417=) c.*60C>A (n.*60C>A) n.3499C>A c.3778C>A (p.Arg1260=) c.*1619C>A (n.*1619C>A) c.3838C>A (p.Arg1280=) n.3545C>A c.4090C>A (p.Arg1364=) c.3991C>A (p.Arg1331=) c.4405C>A (p.Arg1469=) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.9763296A>C | CA394705577 | GRIN2A | c.4248T>G (p.Ser1416Arg) c.*59T>G (n.*59T>G) n.3498T>G c.3777T>G (p.Ser1259Arg) c.*1618T>G (n.*1618T>G) c.3837T>G (p.Ser1279Arg) n.3544T>G c.4089T>G (p.Ser1363Arg) c.3990T>G (p.Ser1330Arg) c.4404T>G (p.Ser1468Arg) | |
16 | g.9763296A>G | CA493692555 | GRIN2A | c.4248T>C (p.Ser1416=) c.*59T>C (n.*59T>C) n.3498T>C c.3777T>C (p.Ser1259=) c.*1618T>C (n.*1618T>C) c.3837T>C (p.Ser1279=) n.3544T>C c.4089T>C (p.Ser1363=) c.3990T>C (p.Ser1330=) c.4404T>C (p.Ser1468=) | |
16 | g.9763296A>T | CA394705580 | GRIN2A | c.4248T>A (p.Ser1416Arg) c.*59T>A (n.*59T>A) n.3498T>A c.3777T>A (p.Ser1259Arg) c.*1618T>A (n.*1618T>A) c.3837T>A (p.Ser1279Arg) n.3544T>A c.4089T>A (p.Ser1363Arg) c.3990T>A (p.Ser1330Arg) c.4404T>A (p.Ser1468Arg) | dbSNP |
16 | g.9763297C>A | CA394705582 | GRIN2A | c.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 |
16 | g.9763297C= | CA2206692651 | GRIN2A | c.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=) | |
16 | g.9763297C>G | CA394705584 | GRIN2A | c.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 |
16 | g.9763297C>T | CA7896189 | GRIN2A | c.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 |
16 | g.9763298T>A | CA394705588 | GRIN2A | c.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) | |
16 | g.9763298T>C | CA394705590 | GRIN2A | c.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 |
16 | g.9763298T>G | CA394705591 | GRIN2A | c.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 |
16 | g.9763299G>A | CA493692559 | GRIN2A | c.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 |
16 | g.9763299G>C | CA394705593 | GRIN2A | c.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 |
16 | g.9763299G= | CA2206692652 | GRIN2A | c.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=) | |
16 | g.9763299G>T | CA7896190 | GRIN2A | c.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 |
16 | g.9763300T>A | CA394705598 | GRIN2A | c.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) | |
16 | g.9763300T>C | CA394705600 | GRIN2A | c.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) | |
16 | g.9763300T>G | CA394705596 | GRIN2A | c.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) | |
16 | g.9763301C>A | CA394705602 | GRIN2A | c.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 |
16 | g.9763301C>G | CA394705604 | GRIN2A | c.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) | |
16 | g.9763301C>T | CA394705606 | GRIN2A | c.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 |
16 | g.9763302C>A | CA394705608 | GRIN2A | c.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 |
16 | g.9763302C>G | CA394705610 | GRIN2A | c.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) | |
16 | g.9763302C>T | CA493692565 | GRIN2A | c.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 |
16 | g.9763303C>A | CA394705617 | GRIN2A | c.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 |
16 | g.9763303C= | CA2206692653 | GRIN2A | c.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=) | |
16 | g.9763303C>G | CA394705613 | GRIN2A | c.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 |
16 | g.9763303C>T | CA394705615 | GRIN2A | c.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 |
16 | g.9763304T>A | CA394705619 | GRIN2A | c.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) | |
16 | g.9763304T>C | CA277535897 | GRIN2A | c.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 |
16 | g.9763304T>G | CA493692566 | GRIN2A | c.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=) | |
16 | g.9763304T= | CA2206692654 | GRIN2A | c.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=) | |
16 | g.9763305G>A | CA493692567 | GRIN2A | c.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 |
16 | g.9763305G>C | CA493692569 | GRIN2A | c.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 |
16 | g.9763305G>T | CA493692570 | GRIN2A | c.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 |
16 | g.9763306G>A | CA394705623 | GRIN2A | c.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 |
16 | g.9763306G>C | CA394705625 | GRIN2A | c.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 |
16 | g.9763306G>T | CA394705627 | GRIN2A | c.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 |
16 | g.9763307A>C | CA394705633 | GRIN2A | c.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) | |
16 | g.9763307A>G | CA394705631 | GRIN2A | c.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 |
16 | g.9763307A>T | CA394705629 | GRIN2A | c.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 |
16 | g.9763308A= | CA2206692655 | GRIN2A | c.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=) | |
16 | g.9763308A>C | CA394705636 | GRIN2A | c.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) | |
16 | g.9763308A>G | CA493692571 | GRIN2A | c.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 |
16 | g.9763308A>T | CA394705638 | GRIN2A | c.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 |
16 | g.9763309C>A | CA394705640 | GRIN2A | c.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 |
16 | g.9763309C= | CA2206692656 | GRIN2A | c.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=) | |
16 | g.9763309C>G | CA394705641 | GRIN2A | c.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 |
16 | g.9763309C>T | CA394705643 | GRIN2A | c.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 |
16 | g.9763310A= | CA2206692657 | GRIN2A | c.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=) | |
16 | g.9763310A>C | CA394705645 | GRIN2A | c.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) | |
16 | g.9763310A>G | CA394705646 | GRIN2A | c.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 |
16 | g.9763310A>T | CA394705648 | GRIN2A | c.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 |
16 | g.9763311G>A | CA493692574 | GRIN2A | c.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 |
16 | g.9763311G>C | CA394705651 | GRIN2A | c.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 |
16 | g.9763311G>T | CA394705652 | GRIN2A | c.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) | |
16 | g.9763312T>A | CA394705656 | GRIN2A | c.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 |
16 | g.9763312T>C | CA394705657 | GRIN2A | c.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 |
16 | g.9763312T>G | CA394705659 | GRIN2A | c.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 |
16 | g.9763313A>C | CA394705661 | GRIN2A | c.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 |
16 | g.9763313A>G | CA394705662 | GRIN2A | c.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 |
16 | g.9763313A>T | CA394705664 | GRIN2A | c.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 |
16 | g.9763314C>A | CA493692577 | GRIN2A | c.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 |
16 | g.9763314C= | CA2206692658 | GRIN2A | c.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=) | |
16 | g.9763314C>G | CA493692578 | GRIN2A | c.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 |
16 | g.9763314C>T | CA7896191 | GRIN2A | c.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 |
16 | g.9763315G>A | CA394705667 | GRIN2A | c.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 |
16 | g.9763315G>C | CA394705670 | GRIN2A | c.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 |
16 | g.9763315G= | CA2206692659 | GRIN2A | c.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=) | |
16 | g.9763315G>T | CA394705671 | GRIN2A | c.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 |
16 | g.9763316A>C | CA394705673 | GRIN2A | c.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) | |
16 | g.9763316A>G | CA394705675 | GRIN2A | c.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) | |
16 | g.9763316A>T | CA394705676 | GRIN2A | c.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) | |
16 | g.9763317T>A | CA493692584 | GRIN2A | c.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 |
16 | g.9763317T>C | CA7896192 | GRIN2A | c.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 |
16 | g.9763317T>G | CA493692583 | GRIN2A | c.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 |
16 | g.9763317T= | CA2206692660 | GRIN2A | c.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=) | |
16 | g.9763318G>A | CA394705680 | GRIN2A | c.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 |
16 | g.9763318G>C | CA394705682 | GRIN2A | c.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 |
16 | g.9763318G>T | CA394705684 | GRIN2A | c.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 |
16 | g.9763319C>A | CA394705686 | GRIN2A | c.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 |
16 | g.9763319C= | CA2206692661 | GRIN2A | c.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=) | |
16 | g.9763319C>G | CA394705688 | GRIN2A | c.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 |
16 | g.9763319C>T | CA394705690 | GRIN2A | c.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 |
16 | g.9763320C>A | CA493692585 | GRIN2A | c.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 |
16 | g.9763320C= | CA2206692662 | GRIN2A | c.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=) | |
16 | g.9763320C>G | CA493692586 | GRIN2A | c.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=) | |
16 | g.9763320C>T | CA7896193 | GRIN2A | c.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 |
16 | g.9763321G>A | CA7896194 | GRIN2A | c.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 |
16 | g.9763321G>C | CA394705694 | GRIN2A | c.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 |
16 | g.9763321G= | CA2206692663 | GRIN2A | c.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=) | |
16 | g.9763321G>T | CA394705696 | GRIN2A | c.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 |
16 | g.9763322T>A | CA394705697 | GRIN2A | c.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 |
16 | g.9763322T>C | CA394705699 | GRIN2A | c.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 |
16 | g.9763322T>G | CA394705701 | GRIN2A | c.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 |
16 | g.9763323T>A | CA493692592 | GRIN2A | c.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 |
16 | g.9763323T>C | CA493692590 | GRIN2A | c.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 |
16 | g.9763323T>G | CA493692591 | GRIN2A | c.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 |
16 | g.9763324G>A | CA7896195 | GRIN2A | c.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 |
16 | g.9763324G>C | CA394705706 | GRIN2A | c.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 |
16 | g.9763324G= | CA2206692664 | GRIN2A | c.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=) | |
16 | g.9763324G>T | CA394705703 | GRIN2A | c.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 |
16 | g.9763325A>C | CA394705709 | GRIN2A | c.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 |
16 | g.9763325A>G | CA394705711 | GRIN2A | c.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 |
16 | g.9763325A>T | CA394705714 | GRIN2A | c.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 |
16 | g.9763326C>A | CA394705716 | GRIN2A | c.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 |
16 | g.9763326C= | CA2206692665 | GRIN2A | c.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=) | |
16 | g.9763326C>G | CA394705718 | GRIN2A | c.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 |
16 | g.9763326C>T | CA7896196 | GRIN2A | c.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 |
16 | g.9763326_9763327insAAACCTAGGGAGCTAGACCTTAGCAGGCCCTCCCGGAGCATAAGC | CA2805819919 | GRIN2A | c.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) | |
16 | g.9763327C>A | CA394705722 | GRIN2A | c.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 |
16 | g.9763327C= | CA2206692666 | GRIN2A | c.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=) | |
16 | g.9763327C>G | CA394705726 | GRIN2A | c.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) | |
16 | g.9763327C>T | CA394705724 | GRIN2A | c.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 |
16 | g.9763328T>A | CA394705728 | GRIN2A | c.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 |
16 | g.9763328T>C | CA394705730 | GRIN2A | c.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 |
16 | g.9763328T>G | CA493692465 | GRIN2A | c.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=) | |
16 | g.9763329C>A | CA394705733 | GRIN2A | c.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 |
16 | g.9763329C= | CA2206692667 | GRIN2A | c.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=) | |
16 | g.9763329C>G | CA394705735 | GRIN2A | c.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 |
16 | g.9763329C>T | CA493692466 | GRIN2A | c.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 |
16 | g.9763330A= | CA2206692668 | GRIN2A | c.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=) | |
16 | g.9763330A>C | CA394705738 | GRIN2A | c.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) | |
16 | g.9763330A>G | CA394705740 | GRIN2A | c.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 |
16 | g.9763330A>T | CA394705741 | GRIN2A | c.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 |
16 | g.9763331A>C | CA394705744 | GRIN2A | c.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) | |
16 | g.9763331A>G | CA493692470 | GRIN2A | c.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 |
16 | g.9763331A>T | CA394705745 | GRIN2A | c.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 |
16 | g.9763332G>A | CA493692471 | GRIN2A | c.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 |
16 | g.9763332G>C | CA493692472 | GRIN2A | c.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 |
16 | g.9763332G= | CA2206692669 | GRIN2A | c.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=) | |
16 | g.9763332G>T | CA7896197 | GRIN2A | c.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 |
16 | g.9763333G>A | CA277535949 | GRIN2A | c.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 |
16 | g.9763333G>C | CA394705752 | GRIN2A | c.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 |
16 | g.9763333G= | CA2206692670 | GRIN2A | c.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=) | |
16 | g.9763333G>T | CA394705750 | GRIN2A | c.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) | |
16 | g.9763334A>C | CA394705755 | GRIN2A | c.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) | |
16 | g.9763334A>G | CA394705759 | GRIN2A | c.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 |
16 | g.9763334A>T | CA394705757 | GRIN2A | c.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 |
16 | g.9763335C>A | CA493692476 | GRIN2A | c.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 |
16 | g.9763335C= | CA2206692671 | GRIN2A | c.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=) | |
16 | g.9763335C>G | CA493692477 | GRIN2A | c.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 |
16 | g.9763335C>T | CA7896198 | GRIN2A | c.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 |
16 | g.9763336G>A | CA394705766 | GRIN2A | c.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 |
16 | g.9763336G>C | CA394705763 | GRIN2A | c.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 |
16 | g.9763336G= | CA2206692672 | GRIN2A | c.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=) | |
16 | g.9763336G>T | CA394705765 | GRIN2A | c.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 |
16 | g.9763337A>C | CA394705769 | GRIN2A | c.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) | |
16 | g.9763337A>G | CA394705771 | GRIN2A | c.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 |
16 | g.9763337A>T | CA394705773 | GRIN2A | c.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 |
16 | g.9763338C>A | CA493692483 | GRIN2A | c.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 |
16 | g.9763338C>G | CA493692484 | GRIN2A | c.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 |
16 | g.9763338C>T | CA493692485 | GRIN2A | c.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 |
16 | g.9763339C>A | CA394705775 | GRIN2A | c.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 |
16 | g.9763339C= | CA2206692673 | GRIN2A | c.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=) | |
16 | g.9763339C>G | CA394705777 | GRIN2A | c.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 |
16 | g.9763339C>T | CA7896199 | GRIN2A | c.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 |
16 | g.9763340G>A | CA277535958 | GRIN2A | c.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 |
16 | g.9763340G>C | CA394705781 | GRIN2A | c.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 |
16 | g.9763340G= | CA2206692674 | GRIN2A | c.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=) | |
16 | g.9763340G>T | CA493692489 | GRIN2A | c.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 |
16 | g.9763341A>C | CA493692490 | GRIN2A | c.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=) | |
16 | g.9763341A>G | CA493692491 | GRIN2A | c.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=) | |
16 | g.9763341A>T | CA493692493 | GRIN2A | c.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=) |