Transcript #00006972 (NM_003907.2, EIF2B5 gene)

Transcript name eukaryotic translation initiation factor 2B, subunit 5 epsilon, 82kDa
Gene name EIF2B5 (eukaryotic translation initiation factor 2B, subunit 5 epsilon, 82kDa)
Chromosome 3
Transcript - NCBI ID NM_003907.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_003898.2
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

70 entries on 1 page. Showing entries 1 - 70.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.134C>G r.(?) p.(Ala45Gly)
?/. - c.135A>G r.(?) p.(Ala45=)
?/. - c.163C>T r.(?) p.(Arg55Cys)
+/. ? c.185A>T r.(?) p.(Asp62Val)
+/. ? c.203T>C r.(?) p.(Leu68Ser)
+/. ? c.218T>G r.(?) p.(Val73Gly)
+/. ? c.220G>A r.(?) p.(Ala74Thr)
-?/. - c.299C>T r.(?) p.(Ala100Val)
-?/. - c.299C>T r.(?) p.(Ala100Val)
+/. - c.318A>T r.(?) p.(Leu106Phe)
+/. - c.318A>T r.(?) p.(Leu106Phe)
+/. ? c.318A>T r.(?) p.(Leu106Phe)
+/. ? c.337C>T r.(?) p.(Arg113Cys)
?/. - c.338G>A r.(?) p.(Arg113His)
+/. - c.338G>A r.(?) p.(Arg113His)
+/. ? c.338G>A r.(?) p.(Arg113His)
+/. ? c.338G>A r.(?) p.(Arg113His)
+?/. - c.407G>A r.(?) p.(Arg136His)
?/. - c.514C>T r.(?) p.(Arg172Trp)
?/. - c.514C>T r.(?) p.(Arg172Trp)
+/. - c.530dup r.(?) p.(Asn177LysfsTer31)
+/. ? c.583C>T r.(?) p.(Arg195Cys)
+/. - c.584G>A r.(?) p.(Arg195His)
+/. ? c.584G>A r.(?) p.(Arg195His)
?/. - c.601G>A r.(?) p.(Val201Met)
?/. - c.668G>C r.(?) p.(Arg223Pro)
?/. 5 c.745A>T r.(?) p.(Ile249Phe)
+/. ? c.805C>G r.(?) p.(Arg269Gly)
+/. 6 c.806G>A r.(?) p.(Arg269Gln)
+/. ? c.806G>A r.(?) p.(Arg269Gln)
+/. ? c.808G>C r.(?) p.(Asp270His)
+/. ? c.896G>A r.(?) p.(Arg299His)
+/. ? c.929G>T r.(?) p.(Cys310Phe)
+/. ? c.943C>G r.(?) p.(Arg315Gly)
+/. ? c.943C>T r.(?) p.(Arg315Cys)
+/. - c.944G>A r.(?) p.(Arg315His)
+/. ? c.944G>A r.(?) p.(Arg315His)
+/. - c.946C>T r.(?) p.(Arg316Ter)
+?/. 7 c.947G>A r.(?) p.(Arg316Gln)
-?/. - c.966C>G r.(?) p.(Thr322=)
+/. ? c.1003T>C r.(?) p.(Cys335Arg)
+/. ? c.1004G>C r.(?) p.(Cys335Ser)
+/. - c.1015C>T r.(?) p.(Arg339Trp)
+/. - c.1015C>T r.(?) p.(Arg339Trp)
+/. ? c.1015C>T r.(?) p.(Arg339Trp)
+/. - c.1016G>A r.(?) p.(Arg339Gln)
+/. ? c.1016G>A r.(?) p.(Arg339Gln)
+/. ? c.1016G>C r.(?) p.(Arg339Pro)
+/. ? c.1016G>C r.(?) p.(Arg339Pro)
?/. - c.1031G>A r.(?) p.(Arg344Gln)
?/. - c.1055A>G r.(?) p.(His352Arg)
+/. ? c.1126A>G r.(?) p.(Asn376Asp)
+/. ? c.1157G>T r.(?) p.(Gly386Val)
+/. ? c.1157G>T r.(?) p.(Gly386Val)
+?/. - c.1208C>T r.(?) p.(Ala403Val)
+?/. - c.1208C>T r.(?) p.(Ala403Val)
+/. ? c.1289T>C r.(?) p.(Val430Ala)
+/. ? c.1340C>T r.(?) p.(Ser447Leu)
-?/. - c.1341G>A r.(?) p.(=)
+/. - c.1444+2T>C r.spl? p.?
-?/. - c.1546+6C>A r.(=) p.(=)
-/. - c.1686G>A r.(?) p.(Gln562=)
-?/. - c.1686G>A r.(?) p.(Gln562=)
?/. - c.1709C>T r.(?) p.(Ser570Phe)
-/. - c.1759A>G r.(?) p.(Ile587Val)
-/. - c.1759A>G r.(?) p.(Ile587Val)
?/. - c.1915G>A r.(?) p.(Ala639Thr)
-?/. - c.1915G>A r.(?) p.(Ala639Thr)
?/. - c.1934C>T r.(?) p.(Ala645Val)
+/. ? c.1948G>A r.(?) p.(Glu650Lys)
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