Transcript #00023814 (NM_004456.4, EZH2 gene)

Transcript name transcript variant 1
Gene name EZH2 (enhancer of zeste homolog 2 (Drosophila))
Chromosome 7
Transcript - NCBI ID NM_004456.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_004447.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2013-05-17 15:00:38 +02:00 (CEST)
Date last edited N/A


Variants

202 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. 1 c.-168dup r.(?) p.(=)
+/. - c.2195+647_*274[0] r.? p.?
+?/? - c.? r.(?) p.(Asn640)
+?/? - c.? r.(?) p.(Asn640)
?/. - c.29A>G r.(?) p.(Lys10Arg)
+/? 2 c.73C>T r.(?) p.(Arg25*)
+/. - c.74G>A r.(?) p.(Arg25Gln)
+/. - c.74G>A r.(?) p.(Arg25Gln)
+/. - c.74G>A r.(?) p.(Arg25Gln)
-/. 2i c.118-63G>A r.(=) p.(=)
-/. - c.118-4del r.spl? p.?
-/. 2i c.118-4del r.spl? p.?
-?/. - c.118-4del r.spl? p.?
-?/. - c.118-4dup r.spl? p.?
?/. - c.134A>G r.(?) p.(Asn45Ser)
+/? 3 c.172C>T r.(?) p.(Gln58*)
+/? 3 c.184C>T r.(?) p.(Gln62*)
?/. - c.188G>A r.(?) p.(Arg63Gln)
+/? 3 c.190dup r.(?) p.(Arg64Lysfs*18)
+/? 3 c.216_217del r.(?) p.(Ser73Cysfs*8)
-?/. - c.234C>T r.(?) p.(Arg78=)
-/. 3i c.246+37T>C r.(=) p.(=)
-/. 3i c.247-80G>A r.(=) p.(=)
-?/. - c.247-10dup r.(=) p.(=)
+/. - c.390C>A r.(?) p.(Asn130Lys)
+/+ 5 c.394C>T r.(?) p.(Pro132Ser)
+?/+ 5 c.394C>T r.(?) p.(Pro132Ser)
-?/. - c.396T>C r.(?) p.(Pro132=)
-/. - c.396T>C r.(?) p.(Pro132=)
-?/. - c.396T>C r.(?) p.(Pro132=)
+/. - c.397T>C r.(?) p.(Tyr133His)
+/. - c.397T>C r.(?) p.(Tyr133His)
+?/+ 5 c.398A>G r.(?) p.(Tyr133Cys)
+?/+ 5 c.398A>G r.(?) p.(Tyr133Cys)
+/? 5 c.401T>C r.(?) p.(Met134Thr)
+/? 5 c.434T>G r.(?) p.(Phe145Cys)
+/. - c.435C>G r.(?) p.(Phe145Leu)
+/. - c.442G>A r.(?) p.(Glu148Lys)
+/? 5 c.442_444dup r.(?) p.(Glu148dup)
+/. - c.443A>G r.(?) p.(Glu148Gly)
+?/. - c.457T>C r.(?) p.(Tyr153His)
+/+ 5 c.457_459del r.(?) p.(Tyr153del)
+/. - c.458A>G r.(?) p.(Tyr153Cys)
+/. 5 c.458A>G r.(?) p.(Tyr153Cys)
?/. - c.464G>A r.(?) p.(Gly155Glu)
+/. - c.466A>G r.(?) p.(Lys156Glu)
+/. - c.466A>G r.(?) p.(Lys156Glu)
+/. - c.466A>G r.(?) p.(Lys156Glu)
+/. - c.466A>G r.(?) p.(Lys156Glu)
+/. - c.466A>G r.(?) p.(Lys156Glu)
+/. - c.466A>G r.(?) p.(Lys156Glu)
+?/. - c.469delinsTCATACA r.(?) p.(Val157delinsSerTyrIle)
+/. - c.475G>A r.(?) p.(Gly159Arg)
+?/. - c.475G>A r.(?) p.(Gly159Arg)
-/. - c.484+13C>T r.(=) p.(=)
-?/. - c.485-7G>A r.(=) p.(=)
-?/. - c.552_554del r.(?) p.(Asp189del)
-/. - c.553G>C r.(?) p.(Asp185His)
-/. 6 c.553G>C r.(?) p.(Asp185His)
?/? 6 c.553G>C r.(?) p.(Asp185His)
?/? 6 c.553G>C r.(?) p.(Asp185His)
+/? 6 c.574G>A r.(?) p.(Asp192Asn)
+/? 6 c.619C>T r.(?) p.(Arg207*)
?/. - c.634A>G r.(?) p.(Ser212Gly)
-?/. - c.657T>C r.(?) p.(Pro219=)
?/. - c.659C>T r.(?) p.(Ser220Phe)
?/. - c.659C>T r.(?) p.(Ser220Phe)
?/. - c.676G>A r.(?) p.(Ala226Thr)
+/. - c.698A>T r.(?) p.(Asp233Val)
+/. - c.698A>T r.(?) p.(Asp233Val)
?/. - c.707C>T r.(?) p.(Thr236Ile)
+/? 7 c.727A>C r.(?) p.(Lys243Gln)
+/? 7i c.729-2del r.spl? p.?
+/? 8 c.730T>G r.(?) p.(Tyr244Asp)
+/? 8 c.745G>A r.(?) p.(Glu249Lys)
+/? 8 c.754C>G r.(?) p.(Leu252Val)
+/? 8 c.758dup r.(?) p.(Gly254Argfs*6)
+/? 8 c.763G>A r.(?) p.(Ala255Thr)
?/. - c.766C>G r.(?) p.(Leu256Val)
+/? 8 c.786dup r.(?) p.(Asn263Glnfs*8)
./. - c.835C>T r.(?) p.(His279Tyr)
+/. - c.835C>T r.(?) p.(His279Tyr)
+?/. - c.835C>T r.(?) p.(His279Tyr)
+?/. - c.836A>G r.(?) p.(His279Arg)
+/? 8 c.836A>G r.(?) p.(His279Arg)
+/? 8 c.863G>A r.(?) p.(Arg288Gln)
?/. - c.868T>G r.(?) p.(Phe290Val)
+/? 8 c.890A>G r.(?) p.(His297Arg)
?/. - c.907+5G>A r.spl? p.?
?/. - c.907+5G>A r.spl? p.?
+/? 9 c.949G>T r.(?) p.(Glu317*)
-?/. - c.965A>G r.(?) p.(Asn322Ser)
+/? 9 c.965A>G r.(?) p.(Asn322Ser)
+/? 9 c.982C>T r.(?) p.(Gln328*)
+/? 10 c.1033G>A r.(?) p.(Ala345Thr)
?/. - c.1100G>A r.(?) p.(Ser367Asn)
+/? 10 c.1176_1177del r.(?) p.(Glu392Aspfs*7)
?/. - c.1198_1200del r.(?) p.(Lys400del)
?/. - c.1198_1200del r.(?) p.(Lys400del)
+/? 10 c.1200_1203del r.(?) p.(Glu401Lysfs*22)
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