Transcript #00008942 (NM_000834.3, GRIN2B gene)

Transcript name glutamate receptor, ionotropic, N-methyl D-aspartate 2B
Gene name GRIN2B (glutamate receptor, ionotropic, N-methyl D-aspartate 2B)
Chromosome 12
Transcript - NCBI ID NM_000834.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000825.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

329 entries on 4 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. 1i_2i c.(?_-18-20840)_(411+32732_?)del r.? p.?
-/. - c.-18-10G>C r.(=) p.(=)
-/. - c.-15G>A r.(?) p.(=)
+/. 9i_13_ c.(?_2010+11766)_*1307{0} r.? p.?
+/. 4i_13_ c.1125+14389_*1307{0} r.? p.?
+/. 2i_13_ c.412-48969_*1307{1} r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
-/. - c.15G>A r.(?) p.(Ala5=)
-?/. - c.20G>A r.(?) p.(Cys7Tyr)
-?/. - c.33G>A r.(?) p.(Lys11=)
+/. - c.99dup r.(?) p.(Ser34GlnfsTer25)
+/. - c.99dup r.(?) p.(Ser34Glnfs*25)
-?/. 2 c.117C>T r.(=) p.(=)
./. - c.140A>G r.(?) p.(Glu47Gly)
./. - c.140A>G r.(?) p.(Glu47Gly)
?/. - c.140A>G r.(?) p.(Glu47Gly)
-?/. - c.140A>G r.(?) p.(Glu47Gly)
?/. - c.162C>G r.(?) p.(His54Gln)
-?/. 2 c.189C>T r.(=) p.(=)
-?/. - c.228C>T r.(?) p.(Thr76=)
-?/. - c.228C>T r.(?) p.(Thr76=)
-?/. 2 c.228C>T r.(=) p.(=)
?/. - c.230A>G r.(?) p.(Asp77Gly)
?/. - c.257G>A r.(?) p.(Cys86Tyr)
+?/. - c.284del r.(?) p.(Gln95ArgfsTer38)
-?/. - c.324C>T r.(?) p.(Ile108=)
-?/. - c.343A>T r.(?) p.(Ile115Phe)
-?/. - c.360C>T r.(?) p.(Leu120=)
-/. - c.366C>G r.(?) p.(Pro122=)
-/. 2 c.366C>G r.366c>g p.Pro122=
-/. 2 c.366C>G r.366c>g p.Pro122=
-/. - c.366C>G r.(?) p.(Pro122=)
?/. - c.382G>A r.(?) p.(Gly128Arg)
?/. - c.401T>C r.(?) p.(Met134Thr)
+/. 2i c.411+1G>A r.0 p.0
+/. 2i c.(411+1_411+50000)delinsN[?] r.? p.?
+/. - c.448A>G r.(?) p.(Ile150Val)
+/. - c.448A>G r.(?) p.(Ile150Val)
-?/. - c.465C>A r.(?) p.(Ser155=)
-/. - c.504C>A r.(?) p.(Ile168=)
+/. - c.538C>T r.(?) p.(Gln180*)
-?/. - c.542A>C r.(?) p.(Asp181Ala)
+/. - c.591G>A r.(?) p.(Trp197Ter)
+?/. - c.649C>T r.(?) p.(Gln217*)
+?/. - c.737C>A r.(?) p.(Ser246*)
+/. - c.737C>A r.(?) p.(Ser246*)
?/. - c.752G>A r.(?) p.(Gly251Asp)
+/. 3 c.803_804del r.803_804del p.Thr268Serfs*15
-?/. - c.812C>T r.(?) p.(Ala271Val)
?/. - c.919A>G r.(?) p.(Met307Val)
?/. - c.991C>A r.(?) p.(Gln331Lys)
+/. 3i_10_ c.(?_1011-25)_(2130_?)del r.? p.?
+?/. - c.1088del r.(?) p.(Val363Glyfs*2)
-?/. 13 c.1116G>A r.(=) p.(=)
+/. - c.1119G>A r.(?) p.(Trp373*)
+/. 4i c.(1125+1_1126-1)delinsN[?] r.? p.?
-/. - c.1125+20A>G r.(=) p.(=)
-/. - c.1126-12A>G r.(=) p.(=)
-?/. 4i c.1126-12A>G r.(=) p.(=)
+?/. - c.1177C>T r.(?) p.(Arg393*)
+/. - c.1238A>G r.(?) p.(Glu413Gly)
-?/. - c.1287C>T r.(?) p.(=)
+?/. - c.1295A>T r.(?) p.(Asn432Ile)
+/. - c.1306T>C r.(?) p.(Cys436Arg)
-/. - c.1329-140G>A r.(=) p.(=)
./. - c.1349C>T r.(?) p.(Pro450Leu)
+/. - c.1367G>A r.(?) p.(Cys456Tyr)
+/. - c.1368C>A r.(?) p.(Cys456*)
+?/. - c.1375G>A r.(?) p.(Gly459Arg)
+/. - c.1382G>T r.(?) p.(Cys461Phe)
+?/. 7 c.1463A>T r.(?) p.(Lys488Met)
+/. - c.1495G>A r.(?) p.(Gly499Arg)
+?/. - c.1537C>T r.(?) p.(Leu513Phe)
+/. - c.1540A>G r.(?) p.(Thr514Ala)
+/. - c.1547A>G r.(?) p.(Asn516Ser)
+?/. - c.1555C>T r.(?) p.(Arg519Ter)
+/. - c.1555C>T r.(?) p.(Arg519Ter)
-?/. 7 c.1560G>A r.(=) p.(=)
?/. - c.1570G>A r.(?) p.(Asp524Asn)
+/. - c.1573T>G r.(?) p.(Phe525Val)
+?/. - c.1583C>T r.(?) p.(Pro528Leu)
?/. - c.1590A>G r.(?) p.(Ile530Met)
+?/. - c.1598G>A r.(?) p.(Gly533Asp)
+?/. - c.1598G>T r.(?) p.(Gly533Val)
+/. - c.1606G>A r.(?) p.(Val536Ile)
+/. - c.1619G>A r.(?) p.(Arg540His)
+/. - c.1619G>A r.(?) p.(Arg540His)
+/. - c.1619G>A r.(?) p.(Arg540His)
+/. - c.1623C>G r.(?) p.(Ser541Arg)
+?/. - c.1628G>C r.(?) p.(Gly543Ala)
+/. - c.1652T>C r.(?) p.(Leu551Ser)
-/. - c.1655-71A>C r.(=) p.(=)
+/. - c.1657C>A r.(?) p.(Pro553Thr)
+?/. - c.1658C>T r.(?) p.(Pro553Leu)
+/. - c.1659dup r.(?) p.(Phe554IlefsTer4)
?/. - c.1660T>A r.(?) p.(Phe554Ile)
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