Transcript #00001108 (NM_000833.3, GRIN2A gene)

Transcript name transcript variant 2
Gene name GRIN2A (glutamate receptor, ionotropic, N-methyl D-aspartate 2A)
Chromosome 16
Transcript - NCBI ID NM_000833.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000824.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-09-13 13:12:59 +02:00 (CEST)
Date last edited N/A


Variants

414 entries on 5 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.(-45292_-78561)_(414+27616_414+46734)del r.0? p.0?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.? r.? p.?
+/. - c.2T>C r.(?) p.(Met1?)
+/. - c.2T>C r.(?) p.(Met1?)
+/. - c.2T>C r.(?) p.(Met1?)
+/. - c.90dup r.(?) p.(Pro31Serfs*107)
+/. - c.90dup r.(?) p.(Pro31Serfs*107)
+/. - c.90dup r.(?) p.(Pro31Serfs*107)
+/. - c.90dup r.(?) p.(Pro31Serfs*107)
-?/. - c.91C>A r.(?) p.(Pro31Thr)
?/. - c.146G>A r.(?) p.(Arg49His)
+/. - c.165G>A r.(?) p.(Trp55*)
+/. - c.172G>T r.(?) p.(Glu58*)
+/. - c.172G>T r.(?) p.(Glu58*)
+/. - c.176_179dup r.(?) p.(Ala61Glyfs*78)
-?/. - c.222G>A r.(?) p.(Met74Ile)
./. - c.222G>A r.(?) p.(Met74Ile)
-?/. - c.222G>A r.(?) p.(Met74Ile)
+/. - c.236C>G r.(?) p.(Pro79Arg)
./. - c.236C>G r.(?) p.(Pro79Arg)
+?/. - c.331C>T r.(?) p.(Gln111*)
?/. - c.361T>C r.(?) p.(Phe121Leu)
+?/. - c.390del r.(?) p.(Ala131Hisfs*3)
-?/. - c.414+115G>A r.(=) p.(=)
-?/. - c.414+38900C>A r.(=) p.(=)
?/. - c.414+66968T>C r.(=) p.(=)
?/. - c.414+66968T>C r.(=) p.(=)
?/. - c.414+67014G>A r.(=) p.(=)
?/. - c.414+67203C>T r.(=) p.(=)
?/. - c.414+67203C>T r.(=) p.(=)
?/. - c.414+67429C>T r.(=) p.(=)
?/. - c.414+67429C>T r.(=) p.(=)
-?/. - c.415-101530G>A r.(=) p.(=)
-?/. - c.415-101525_415-101524del r.(=) p.(=)
+/. - c.415-2A>G r.spl? p.?
+/. - c.415-2A>G r.(?) p.?
-?/. - c.422C>T r.(?) p.(Thr141Met)
-?/. - c.422C>T r.(?) p.(Thr141Met)
-?/. - c.422C>T r.(?) p.(Thr141Met)
+/. - c.445_448delins(69) r.(?) p.?
+/. - c.487C>T r.(?) p.(Gln163*)
+/. - c.487C>T r.(?) p.(Gln163*)
-?/. - c.498C>G r.(?) p.(Asp166Glu)
?/. - c.498C>G r.(?) p.(Asp166Glu)
+/. - c.500G>A r.(?) p.(Trp167*)
?/. - c.502C>A r.(?) p.(His168Asn)
-?/. - c.547T>A r.(?) p.(Phe183Ile)
./. - c.547T>A r.(?) p.(Phe183Ile)
+/. - c.551T>G r.(?) p.(Ile184Ser)
+/. - c.594G>A r.(?) p.(Trp198*)
+/. - c.594G>A r.(?) p.(Trp198*)
+/. - c.594G>A r.(?) p.(Trp198*)
+/. - c.594G>A r.(?) p.(Trp198*)
+/. - c.594G>A r.(?) p.(Trp198*)
+/. - c.594G>A r.(?) p.(Trp198*)
+/. - c.594G>A r.(?) p.(Trp198*)
+/. - c.594G>A r.(?) p.(Trp198*)
+/. - c.594G>A r.(?) p.(Trp198*)
+/. - c.594G>A r.(?) p.(Trp198*)
?/. 4 c.605A>G r.(?) p.(Asn202Ser)
?/. - c.623C>T r.(?) p.(Thr208Ile)
+/. - c.627del r.(?) p.(Phe210Leufs*10)
+/. - c.627del r.(?) p.(Phe210Leufs*10)
?/. - c.638C>T r.(?) p.(Ala213Val)
+/. 4 c.652C>T r.0 p.0
+/. - c.652C>T r.(?) p.(Gln218*)
-?/. - c.662A>G r.(?) p.(Lys221Arg)
./. - c.692G>A r.(?) p.(Cys231Tyr)
+/. - c.692G>A r.(?) p.(Cys231Tyr)
+/. - c.692G>A r.(?) p.(Cys231Tyr)
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