Transcript #00006885 (NM_001961.3, EEF2 gene)

Transcript name eukaryotic translation elongation factor 2
Gene name EEF2 (eukaryotic translation elongation factor 2)
Chromosome 19
Transcript - NCBI ID NM_001961.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_001952.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

68 entries on 1 page. Showing entries 1 - 68.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.3+2T>C r.spl? p.?
+/. 2 c.34A>G c.34a>g p.Ile12Val
-/. - c.219-13C>T r.(=) p.(=)
-?/. - c.243C>G r.(?) p.(Leu81=)
-?/. - c.288C>T r.(?) p.(Ala96=)
-?/. - c.318C>T r.(?) p.(Pro106=)
-/. - c.324T>C r.(?) p.(His108=)
-/. - c.450C>T r.(?) p.(Arg150=)
-/. - c.486C>T r.(?) p.(Arg162=)
-/. - c.567C>T r.(?) p.(Ile189=)
-/. - c.612+20G>A r.(=) p.(=)
?/. - c.671C>T r.(?) p.(Thr224Ile)
?/. - c.688G>A r.(?) p.(Glu230Lys)
?/. - c.688G>A r.(?) p.(Glu230Lys)
?/. - c.709G>A r.(?) p.(Ala237Thr)
-/. - c.711C>T r.(?) p.(Ala237=)
-?/. - c.712G>A r.(?) p.(Ala238Thr)
?/. - c.767T>C r.(?) p.(Met256Thr)
-?/. - c.898-6A>G r.(=) p.(=)
-/. - c.906T>C r.(?) p.(Asp302=)
?/. - c.968T>C r.(?) p.(Leu323Pro)
-?/. - c.975C>T r.(?) p.(Ser325=)
-?/. - c.1011+5G>A r.spl? p.?
-?/. - c.1011+17G>A r.(=) p.(=)
-?/. - c.1011+17G>A r.(=) p.(=)
?/. - c.1033C>T r.(?) p.(Pro345Ser)
+/. - c.1083del r.(?) p.(Val362Ter)
-?/. - c.1137C>T r.(?) p.(Asp379=)
-/. - c.1150+15T>C r.(=) p.(=)
-?/. - c.1151-5C>G r.spl? p.?
?/. - c.1163G>A r.(?) p.(Cys388Tyr)
?/. - c.1187T>G r.(?) p.(Met396Arg)
-?/. - c.1290G>A r.(?) p.(Met430Ile)
?/. - c.1339A>C r.(?) p.(Ile447Leu)
?/. - c.1453A>G r.(?) p.(Ile485Val)
-?/. - c.1453A>G r.(?) p.(Ile485Val)
-/. - c.1569G>A r.(?) p.(Gly523=)
-?/. - c.1605+11A>G r.(=) p.(=)
-?/. - c.1614C>A r.(?) p.(Ile538=)
-/. - c.1632T>C r.(?) p.(His544=)
-?/. - c.1668C>A r.(?) p.(=)
-?/. - c.1677G>A r.(?) p.(Lys559=)
-?/. - c.1702A>G r.(?) p.(Ile568Val)
-?/. - c.1713+7C>T r.(=) p.(=)
-/. - c.1713+15A>G r.(=) p.(=)
-?/. - c.1725G>A r.(?) p.(Pro575=)
-?/. - c.1779C>A r.(?) p.(Ser593=)
-?/. - c.1842C>T r.(?) p.(Ala614=)
-?/. - c.2019C>T r.(?) p.(Asn673=)
-?/. - c.2067+10G>A r.(=) p.(=)
-?/. - c.2067+10G>A r.(=) p.(=)
-?/. - c.2163C>T r.(?) p.(Ile721=)
-/. - c.2175A>G r.(?) p.(Ala725=)
-/. - c.2190T>C r.(?) p.(Tyr730=)
-?/. - c.2205C>T r.(?) p.(Thr735=)
-?/. - c.2220C>T r.(?) p.(Leu740=)
-/. - c.2250+13C>T r.(=) p.(=)
-?/. - c.2251-19T>A r.(=) p.(=)
+/. - c.2305C>T r.(?) p.(His769Tyr)
-?/. - c.2307C>T r.(?) p.(His769=)
?/. - c.2308G>T r.(?) p.(Val770Leu)
-?/. - c.2383+7G>T r.(=) p.(=)
-?/. - c.2415C>T r.(?) p.(Gly805=)
-?/. - c.2430C>T r.(?) p.(Pro810=)
-?/. - c.2430C>T r.(?) p.(Pro810=)
-?/. - c.2457C>T r.(?) p.(Ile819=)
-?/. - c.2460G>C r.(?) p.(Leu820=)
-/. - c.*3G>A r.(=) p.(=)
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