Transcript #00025331 (NM_007325.4, GRIA3 gene)

Transcript name transcript variant 1
Gene name GRIA3 (glutamate receptor, ionotropic, AMPA 3)
Chromosome X
Transcript - NCBI ID NM_007325.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_015564.4
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2018-10-23 16:18:37 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-3_-1= r.(=) p.(=)
?/. - c.-2dup r.(?) p.(=)
-/. - c.-2dup r.(?) p.(=)
?/. - c.-2dup r.(?) p.(=)
-/. - c.-2G>C r.(?) p.(=)
-/. - c.-2_-1delinsCG r.(?) p.(=)
+/. - c.0 r.0 p.0
?/. - c.2T>C r.(?) p.(Met1?)
-?/. - c.2T>C r.(?) p.(Met1?)
?/. - c.159T>C r.(?) p.(Phe53=)
?/. - c.159T>C r.(?) p.(Phe53=)
-?/. - c.159T>C r.(?) p.(Phe53=)
?/. - c.179C>T r.(?) p.(Thr60Ile)
-?/. - c.179C>T r.(?) p.(Thr60Ile)
-/. - c.268+16761dup r.(=) p.(=)
?/. - c.268+16761dup r.(=) p.(=)
?/. - c.268+16761dup r.(=) p.(=)
-?/. - c.268+16761dup r.(=) p.(=)
-/. - c.268+16761dup r.(=) p.(=)
?/. - c.268+16761dup r.(=) p.(=)
?/. - c.268+16761dup r.(=) p.(=)
-/. - c.268+16762_268+16763insG r.(=) p.(=)
?/. - c.268+18363T>A r.(=) p.(=)
?/. - c.268+18363T>A r.(=) p.(=)
?/. - c.268+18405C>A r.(=) p.(=)
?/. - c.279G>T r.(?) p.(Gln93His)
-?/. - c.397G>A r.(?) p.(Ala133Thr)
?/. - c.413T>C r.(?) p.(Val138Ala)
?/. - c.419A>G r.(?) p.(Gln140Arg)
?/. - c.509-244A>C r.(=) p.(=)
?/. - c.509-244A>C r.(=) p.(=)
?/. - c.573G>T r.(?) p.(Arg191Ser)
?/. - c.580G>A r.(?) p.(Gly194Arg)
-?/. - c.611G>A r.(?) p.(Arg204His)
?/. - c.616A>G r.(?) p.(Ile206Val)
-?/. - c.626T>C r.(?) p.(Met209Thr)
?/. - c.647G>A r.(?) p.(Arg216Gln)
+/. - c.670G>T r.(?) p.(Glu224Ter)
+/. - c.670G>T r.(?) p.(Glu224*)
-?/. - c.696+5G>A r.spl? p.?
?/. - c.696+156del r.(=) p.(=)
?/. - c.696+156del r.(=) p.(=)
?/. - c.696+166_696+173del r.(=) p.(=)
?/. - c.696+169_696+173del r.(=) p.(=)
?/. - c.696+169_696+173del r.(=) p.(=)
-/. - c.751-16T>C r.(=) p.(=)
?/. - c.751-16T>C r.(=) p.(=)
?/. - c.751-16T>C r.(=) p.(=)
?/. - c.753T>C r.(?) p.(=)
?/. - c.785A>G r.(?) p.(His262Arg)
-?/. - c.913-15A>G r.(=) p.(=)
+/. - c.982C>T r.(?) p.(Arg328Ter)
?/. - c.992T>C r.(?) p.(Val331Ala)
-/. - c.1081-38G>A r.(=) p.(=)
-?/. - c.1125T>C r.(?) p.(Tyr375=)
-?/. - c.1166A>C r.(?) p.(Lys389Thr)
-?/. - c.1166A>C r.(?) p.(Lys389Thr)
-?/. - c.1166A>C r.(?) p.(Lys389Thr)
-/. - c.1181G>A r.(?) p.(Arg394Gln)
-/. - c.1181G>A r.(?) p.(Arg394Gln)
-?/. - c.1185+9C>A r.(=) p.(=)
+?/. - c.1190G>A r.(?) p.(Gly397Asp)
-/. - c.1200T>C r.(?) p.(Asn400=)
?/. - c.1200T>C r.(=) p.(=)
-?/. - c.1200T>C r.(?) p.(=)
?/. - c.1200T>C r.(=) p.(=)
?/. - c.1220C>T r.(?) p.(Pro407Leu)
?/. - c.1236A>C r.(?) p.(Gln412His)
-?/. - c.1237A>G r.(?) p.(Ile413Val)
?/. - c.1293+48C>T r.(=) p.(=)
?/. - c.1293+48C>T r.(=) p.(=)
-?/. - c.1326T>C r.(?) p.(His442=)
+/. - c.1349G>A r.(?) p.(Arg450Gln)
+?/. - c.1349G>A r.(?) p.(Arg450Gln)
+?/. - c.1375G>C r.(?) p.(Ala459Pro)
-?/. - c.1501-8T>A r.(=) p.(=)
-?/. - c.1501-8T>A r.(=) p.(=)
-/. - c.1501-5T>C r.spl? p.?
?/. - c.1601T>A r.(?) p.(Ile534Lys)
?/. - c.1609C>G r.(?) p.(Pro537Ala)
+?/. - c.1672del r.(?) p.(Cys558Alafs*11)
?/. - c.1781A>G r.(?) p.(Gln594Arg)
?/. - c.1888G>A r.(?) p.(Gly630Arg)
+?/. - c.1888G>A r.(?) p.(Gly630Arg)
+/. 12 c.1888G>C r.(?) p.(Gly630Arg)
+/. - c.1891C>A r.(?) p.(Arg631Ser)
+?/. - c.1892G>A r.(?) p.(Arg631His)
+/. - c.1957G>A r.(?) p.(Ala653Thr)
?/. - c.1978A>G r.(?) p.(Arg660Gly)
-?/. - c.2076+20T>C r.(=) p.(=)
?/. - c.2076+158C>T r.(=) p.(=)
?/. - c.2076+158C>T r.(=) p.(=)
-/. - c.2077-69del r.(=) p.(=)
+/. - c.2117T>C r.(?) p.(Met706Thr)
?/. 14 c.2117T>C r.(?) p.(Met706Thr)
+/. - c.2161G>A r.(?) p.(Gly721Arg)
+/. - c.2497G>A r.(?) p.(Gly833Arg)
+?/. - c.2497G>A r.(?) p.(Gly833Arg)
-?/. - c.2531T>C r.(?) p.(Ile844Thr)
?/. - c.2638T>A r.(?) p.(Tyr880Asn)
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