Transcript #00026022 (NM_001134407.2, GRIN2A gene)

Transcript name transcript variant 1 (expired, new version available) (expired, new version available)
Gene name GRIN2A (glutamate receptor, ionotropic, N-methyl D-aspartate 2A)
Chromosome 16
Transcript - NCBI ID NM_001134407.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001127879.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2025-10-30 13:30:47 +01:00 (CET)
Date last edited N/A


Variants

160 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.91C>A r.(?) p.(Pro31Thr)
?/. - c.146G>A r.(?) p.(Arg49His)
-?/. - c.222G>A r.(?) p.(Met74Ile)
-?/. - c.222G>A r.(?) p.(Met74Ile)
+/. - c.236C>G r.(?) p.(Pro79Arg)
?/. - 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.415-101530G>A r.(=) p.(=)
-?/. - c.415-101525_415-101524del r.(=) p.(=)
-?/. - c.415-3C>T r.spl? p.?
+/. - c.415-2A>G r.spl? p.?
-?/. - c.422C>T r.(?) p.(Thr141Met)
-?/. - c.422C>T r.(?) p.(Thr141Met)
-?/. - c.422C>T r.(?) p.(Thr141Met)
-?/. - c.498C>G r.(?) p.(Asp166Glu)
?/. - c.498C>G r.(?) p.(Asp166Glu)
?/. - c.502C>A r.(?) p.(His168Asn)
-?/. - c.547T>A r.(?) p.(Phe183Ile)
-?/. - c.547T>A r.(?) p.(Phe183Ile)
?/. - c.623C>T r.(?) p.(Thr208Ile)
+/. - c.627del r.(?) p.(Phe210LeufsTer10)
?/. - c.638C>T r.(?) p.(Ala213Val)
-?/. - c.662A>G r.(?) p.(Lys221Arg)
-?/. - c.741C>T r.(?) p.(Gly247=)
-?/. - c.810A>G r.(?) p.(Lys270=)
-?/. - c.819A>G r.(?) p.(Pro273=)
-?/. - c.819A>G r.(?) p.(Pro273=)
+/. - c.821C>A r.(?) p.(Ser274*)
+/. - c.843C>G r.(?) p.(Tyr281Ter)
?/. - c.854A>C r.(?) p.(Asp285Ala)
-?/. - c.883G>A r.(?) p.(Gly295Ser)
-/. - c.939C>T r.(?) p.(Ile313=)
-?/. - c.942C>T r.(?) p.(Pro314=)
?/. - c.998C>A r.(?) p.(Thr333Asn)
-?/. - c.1006C>T r.(?) p.(Pro336Ser)
-?/. - c.1008-19763A>C r.(=) p.(=)
-?/. - c.1008-16C>G r.(=) p.(=)
+?/. - c.1097T>C r.(?) p.(Leu366Pro)
-/. - c.1122+84G>A r.(=) p.(=)
-?/. - c.1122+133T>C r.(=) p.(=)
+/. - c.1123-1G>T r.spl? p.?
?/. - c.1183T>C r.(?) p.(Ser395Pro)
+/. - c.1204del r.(?) p.(Asp402MetfsTer21)
-?/. - c.1206T>C r.(?) p.(Asp402=)
-/. - c.1275G>A r.(?) p.(Leu425=)
-/. - c.1328+142A>T r.(=) p.(=)
-?/. - c.1329-81A>T r.(=) p.(=)
-?/. - c.1329-9T>G r.(=) p.(=)
-?/. - c.1329-8C>T r.(=) p.(=)
?/. - c.1346G>T r.(?) p.(Gly449Val)
-?/. - c.1354G>A r.(?) p.(Val452Met)
-/. - c.1498-34C>T r.(=) p.(=)
-/. - c.1498-17_1498-14dup r.(=) p.(=)
-?/. - c.1498-15_1498-14del r.(=) p.(=)
-/. - c.1498-15_1498-14del r.(=) p.(=)
-/. - c.1498-15_1498-14dup r.(=) p.(=)
-/. - c.1498-14del r.(=) p.(=)
-/. - c.1498-14del r.(=) p.(=)
-?/. - c.1498-5T>C r.spl? p.?
+/. - c.1510C>T r.(?) p.(Arg504Trp)
?/. - c.1532C>T r.(?) p.(Ser511Leu)
-?/. - c.1533G>A r.(?) p.(Ser511=)
+/. - c.1592C>T r.(?) p.(Thr531Met)
-/. - c.1652-79A>G r.(=) p.(=)
-?/. - c.1652-13T>C r.(=) p.(=)
+/. - c.1655C>G r.(?) p.(Pro552Arg)
?/. - c.1663G>A r.(?) p.(Ala555Thr)
+/. - c.1681_1683del r.(?) p.(Met561del)
?/. - c.1717G>A r.(?) p.(Val573Ile)
-?/. - c.1777+139G>C r.(=) p.(=)
?/. - c.1820T>C r.(?) p.(Leu607Pro)
?/. - c.1834G>T r.(?) p.(Val612Leu)
-?/. - c.1851G>C r.(?) p.(=)
?/. - c.1915G>A r.(?) p.(Val639Ile)
+?/. - c.1943A>G r.(?) p.(Asn648Ser)
+?/. - c.1945C>G r.(?) p.(Leu649Val)
+?/. - c.1959G>A r.(?) p.(Met653Ile)
?/. - c.1990G>A r.(?) p.(Gly664Ser)
-?/. - c.2007+14G>C r.(=) p.(=)
-/. - c.2008-36C>T r.(=) p.(=)
-?/. - c.2008-24_2008-23dup r.(=) p.(=)
+?/. - c.2084G>A r.(?) p.(Arg695Gln)
-/. - c.2085G>C r.(?) p.(Arg695=)
+/. - c.2146G>A r.(?) p.(Ala716Thr)
-?/. - c.2169-41C>T r.(=) p.(=)
-?/. - c.2169-19T>C r.(=) p.(=)
+?/. - c.2169-2A>T r.spl? p.?
-?/. - c.2190C>T r.(?) p.(Tyr730=)
-?/. - c.2190C>T r.(?) p.(Tyr730=)
+/. - c.2211C>A r.(?) p.(Tyr737Ter)
?/. - c.2257G>A r.(?) p.(Gly753Arg)
-?/. - c.2277C>T r.(?) p.(Thr759=)
-?/. - c.2277C>T r.(?) p.(Thr759=)
+?/. - c.2278G>A r.(?) p.(Gly760Ser)
-?/. - c.2356+115T>C r.(=) p.(=)
-?/. - c.2356+138A>G r.(=) p.(=)
-?/. - c.2357-164T>C r.(=) p.(=)
-?/. - c.2441T>C r.(?) p.(Ile814Thr)
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