Transcript #00025967 (NM_012154.3, EIF2C2 gene)

Transcript name transcript variant 1
Gene name EIF2C2 (eukaryotic translation initiation factor 2C, 2)
Chromosome 8
Transcript - NCBI ID NM_012154.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_036286.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2025-01-12 11:09:42 +01:00 (CET)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. _1_3i c.(?_-171995)_(336+642_337-1)del r.0 p.0
-?/. - c.38C>T r.(?) p.(Ala13Val)
?/. - c.50C>A r.(?) p.(Pro17His)
?/. - c.50C>A r.(?) p.(Pro17His)
+/. - c.77C>T r.(?) p.(Pro26Leu)
?/. - c.216-4884A>G r.(=) p.(=)
-?/. - c.220A>G r.(?) p.(Ile74Val)
?/. - c.337-5C>T r.spl? p.?
+/. 4i_5 c.519-24_529del r.spl p.?
+?/. - c.539C>T r.(?) p.(Ser180Phe)
+?/. - c.539C>T r.(?) p.(Ser180Phe)
+?/. - c.539C>T r.(?) p.(Ser180Phe)
+?/. - c.539C>T r.(?) p.(Ser180Phe)
+/. - c.544_546del r.(?) p.(Phe182del)
+/. - c.544_546del r.(?) p.(Phe182del)
+/. - c.544_546del r.(?) p.(Phe182del)
+/. - c.544_546del r.(?) p.(Phe182del)
+/. - c.575T>C r.(?) p.(Leu192Pro)
+/. - c.575T>C r.(?) p.(Leu192Pro)
+?/. - c.579_581del r.(?) p.(Gly195del)
+/. - c.601G>T r.(?) p.(Gly201Cys)
+/. - c.601G>T r.(?) p.(Gly201Cys)
+?/. - c.601G>T r.(?) p.(Gly201Cys)
+/. - c.602G>T r.(?) p.(Gly201Val)
+/. - c.602G>T r.(?) p.(Gly201Val)
+/. - c.602G>T r.(?) p.(Gly201Val)
+/. - c.608A>G r.(?) p.(His203Arg)
+/. - c.609T>A r.(?) p.(His203Gln)
?/. - c.609T>A r.(?) p.(His203Gln)
?/. - c.626C>G r.(?) p.(Ser209Cys)
?/. - c.765G>T r.(?) p.(Arg255Ser)
?/. - c.805A>G r.(?) p.(Ile269Val)
?/. - c.859C>T r.(?) p.(Arg287Trp)
-?/. - c.878+357G>A r.(=) p.(=)
?/. - c.879-4T>C r.spl? p.?
+?/. - c.995A>C r.(?) p.(Gln332Pro)
+/. - c.1070C>T r.(?) p.(Thr357Met)
+/. - c.1070C>T r.(?) p.(Thr357Met)
+/. - c.1070C>T r.(?) p.(Thr357Met)
+/. - c.1070C>T r.(?) p.(Thr357Met)
-?/. - c.1070C>T r.(?) p.(Thr357Met)
+/. - c.1070C>T r.(?) p.(Thr357Met)
?/. - c.1075A>C r.(?) p.(Asn359His)
+?/. - c.1079A>G r.(?) p.(Gln360Arg)
+/. - c.1091T>C r.(?) p.(Met364Thr)
+/. - c.1091T>C r.(?) p.(Met364Thr)
?/. - c.1091T>C r.(?) p.(Met364Thr)
+?/. - c.1092G>A r.(?) p.(Met364Ile)
+?/. - c.1093A>C r.(?) p.(Ile365Leu)
+?/. - c.1093A>G r.(?) p.(Ile365Val)
+?/. - c.1094T>A r.(?) p.(Ile365Asn)
+/. - c.1099G>C r.(?) p.(Ala367Pro)
+?/. - c.1115C>A r.(?) p.(Ala372Glu)
+?/. - c.1244C>T r.(?) p.(Pro415Leu)
-?/. - c.1269+4C>T r.spl? p.?
-?/. - c.1269+4C>T r.spl? p.?
+?/. - c.1303T>C r.(?) p.(Trp435Arg)
-?/. - c.1500C>T r.(?) p.(Ser500=)
+?/. - c.1517G>A r.(?) p.(Arg506Gln)
+?/. - c.1591G>C r.(?) p.(Glu531Gln)
?/. - c.1597A>G r.(?) p.(Lys533Glu)
+?/. - c.1631C>T r.(?) p.(Thr544Met)
+/. - c.1717G>A r.(?) p.(Gly573Ser)
-?/. - c.1749-4G>A r.spl? p.?
+?/. - c.1805C>A r.(?) p.(Pro602His)
+?/. - c.1805C>G r.(?) p.(Pro602Arg)
+?/. - c.1805C>G r.(?) p.(Pro602Arg)
+?/. - c.1810G>A r.(?) p.(Gly604Arg)
+?/. - c.1810G>A r.(?) p.(Gly604Arg)
+?/. - c.1810G>A r.(?) p.(Gly604Arg)
+?/. - c.1810G>A r.(?) p.(Gly604Arg)
+?/. - c.1810G>A r.(?) p.(Gly604Arg)
+?/. - c.1810G>A r.(?) p.(Gly604Arg)
-?/. - c.1839+10A>G r.(=) p.(=)
+?/. - c.1855G>A r.(?) p.(Asp619Asn)
?/. - c.1992C>G r.(?) p.(Ile664Met)
?/. - c.2059A>C r.(?) p.(Ile687Leu)
+?/. - c.2140C>T r.(?) p.(Arg714Trp)
+?/. - c.2140C>T r.(?) p.(Arg714Trp)
+/. - c.2149T>C r.(?) p.(Cys717Arg)
+/. - c.2149T>C r.(?) p.(Cys717Arg)
+/. - c.2149T>C r.(?) p.(Cys717Arg)
+/. - c.2149T>C r.(?) p.(Cys717Arg)
+?/. - c.2185A>C r.(?) p.(Asn729His)
?/. - c.2197G>C r.(?) p.(Gly733Arg)
+/. - c.2252G>A r.(?) p.(Cys751Tyr)
+/. - c.2252G>A r.(?) p.(Cys751Tyr)
+/. - c.2252G>A r.(?) p.(Cys751Tyr)
+?/. - c.2273G>A r.(?) p.(Gly758Glu)
+/. - c.2280C>G r.(?) p.(Ser760Arg)
?/. - c.2281A>T r.(?) p.(Arg761Trp)
?/. - c.2288C>T r.(?) p.(Ser763Leu)
-?/. - c.2318G>A r.(?) p.(Arg773His)
+?/. - c.2348C>T r.(?) p.(Thr783Ile)
+?/. - c.2348C>T r.(?) p.(Thr783Ile)
+?/. - c.2375G>A r.(?) p.(Arg792His)
+?/. - c.2375G>A r.(?) p.(Arg792His)
+?/. - c.2375G>A r.(?) p.(Arg792His)
+?/. - c.2383C>T r.(?) p.(Arg795Cys)
+?/. - c.2402C>T r.(?) p.(Ala801Val)
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