NM_001134407.3(GRIN2A):c.4307A>G (p.Asn1436Ser)
|
rs77029288
|
0.00068
|
NM_001134407.3(GRIN2A):c.3827C>G (p.Ala1276Gly)
|
rs145063086
|
0.00067
|
NM_001134407.3(GRIN2A):c.736C>A (p.Leu246Ile)
|
rs555768104
|
0.00021
|
NM_001134407.3(GRIN2A):c.2636A>G (p.Lys879Arg)
|
rs183029507
|
0.00007
|
NM_001134407.3(GRIN2A):c.3898A>G (p.Arg1300Gly)
|
rs372353067
|
0.00007
|
NM_001134407.3(GRIN2A):c.3103G>A (p.Asp1035Asn)
|
rs540445580
|
0.00006
|
NM_001134407.3(GRIN2A):c.623C>T (p.Thr208Ile)
|
rs367543124
|
0.00006
|
NM_001134407.3(GRIN2A):c.2664G>A (p.Thr888=)
|
rs113847665
|
0.00004
|
NM_001134407.3(GRIN2A):c.883G>A (p.Gly295Ser)
|
rs568484876
|
0.00004
|
NM_001134407.3(GRIN2A):c.989C>T (p.Pro330Leu)
|
rs367543120
|
0.00004
|
NM_001134407.3(GRIN2A):c.3578T>G (p.Leu1193Trp)
|
rs75761674
|
0.00003
|
NM_001134407.3(GRIN2A):c.2543G>A (p.Cys848Tyr)
|
rs779911797
|
0.00002
|
NM_001134407.3(GRIN2A):c.2695C>T (p.Arg899Trp)
|
rs796052553
|
0.00002
|
NM_001134407.3(GRIN2A):c.2908C>T (p.Arg970Trp)
|
rs765257420
|
0.00002
|
NM_001134407.3(GRIN2A):c.3037C>T (p.Leu1013=)
|
rs775262289
|
0.00002
|
NM_001134407.3(GRIN2A):c.1517T>C (p.Val506Ala)
|
rs796052543
|
0.00001
|
NM_001134407.3(GRIN2A):c.1675G>A (p.Val559Met)
|
rs1476673300
|
0.00001
|
NM_001134407.3(GRIN2A):c.171C>T (p.Pro57=)
|
rs781693549
|
0.00001
|
NM_001134407.3(GRIN2A):c.3163G>C (p.Glu1055Gln)
|
rs370107080
|
0.00001
|
NM_001134407.3(GRIN2A):c.3722G>A (p.Arg1241Gln)
|
rs886042648
|
0.00001
|
NM_001134407.3(GRIN2A):c.3809A>T (p.Asp1270Val)
|
rs750649530
|
0.00001
|
NM_001134407.3(GRIN2A):c.495T>C (p.Tyr165=)
|
rs569491666
|
0.00001
|
NM_001134407.3(GRIN2A):c.1329-7dup
|
rs1455515948
|
|
NM_001134407.3(GRIN2A):c.1374G>A (p.Gly458=)
|
rs368221866
|
|
NM_001134407.3(GRIN2A):c.1A>T (p.Met1Leu)
|
|
|
NM_001134407.3(GRIN2A):c.3032G>T (p.Arg1011Leu)
|
rs1163766811
|
|
NM_001134407.3(GRIN2A):c.3064C>A (p.Arg1022Ser)
|
rs560057284
|
|
NM_001134407.3(GRIN2A):c.3178G>A (p.Asp1060Asn)
|
rs879255358
|
|
NM_001134407.3(GRIN2A):c.3391G>T (p.Asp1131Tyr)
|
rs1243412120
|
|
NM_001134407.3(GRIN2A):c.3544G>T (p.Asp1182Tyr)
|
rs375160358
|
|
NM_001134407.3(GRIN2A):c.3712G>A (p.Ala1238Thr)
|
rs2141129928
|
|
NM_001134407.3(GRIN2A):c.3914G>C (p.Ser1305Thr)
|
|
|
NM_001134407.3(GRIN2A):c.4081C>G (p.His1361Asp)
|
rs797045606
|
|
NM_001134407.3(GRIN2A):c.415G>T (p.Asp139Tyr)
|
rs1555455852
|
|
NM_001134407.3(GRIN2A):c.4235G>C (p.Cys1412Ser)
|
rs1900675462
|
|