Transcript #00001269 (NM_006312.5, NCOR2 gene)

Transcript name transcript variant 1
Gene name NCOR2 (nuclear receptor corepressor 2)
Chromosome 12
Transcript - NCBI ID NM_006312.5
Transcript - Ensembl ID -
Protein - NCBI ID NP_006303.4
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2012-09-13 13:22:27 +02:00 (CEST)
Date last edited N/A


Variants

60 entries on 1 page. Showing entries 1 - 60.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-118+5G>A r.spl? p.?
-?/. - c.13A>G r.(?) p.(Thr5Ala)
-?/. - c.390G>C r.(?) p.(Ala130=)
?/. - c.415C>T r.(?) p.(Arg139Cys)
?/. - c.420C>A r.(?) p.(Ser140Arg)
?/. - c.567G>C r.(?) p.(Gln189His)
-?/. - c.591+3G>A r.spl? p.?
-?/. - c.843C>T r.(?) p.(Ile281=)
-?/. - c.883-10G>A r.(=) p.(=)
-?/. - c.1086C>T r.(?) p.(Ser362=)
?/. - c.1096G>A r.(?) p.(Ala366Thr)
-/. - c.1523_1531dup r.(?) p.(Gln508_Gln510dup)
?/. - c.1523_1531dup r.(?) p.(Gln508_Gln510dup)
-/. - c.1526_1531dup r.(?) p.(Gln509_Gln510dup)
-/. - c.1526_1531dup r.(?) p.(Gln509_Gln510dup)
-?/. - c.1587G>A r.(?) p.(Ala529=)
-?/. - c.1607C>T r.(?) p.(Pro536Leu)
-?/. - c.1611G>A r.(?) p.(Glu537=)
?/. - c.1870A>C r.(?) p.(Lys624Gln)
?/. - c.2035G>A r.(?) p.(Ala679Thr)
?/. - c.2063C>T r.(?) p.(Ala688Val)
?/. - c.2167G>A r.(?) p.(Ala723Thr)
?/. - c.2796C>T r.(?) p.(Gly932=)
-?/. - c.2951C>T r.(?) p.(Pro984Leu)
-?/. - c.3021G>A r.(?) p.(Pro1007=)
?/. - c.3101C>A r.(?) p.(Ala1034Asp)
-?/. - c.3106G>A r.(?) p.(Ala1036Thr)
?/. - c.3179G>A r.(?) p.(Arg1060His)
+?/. - c.3419_3428del r.(?) p.(His1140Profs*25)
-?/. - c.3453G>T r.(?) p.(Gly1151=)
?/. - c.3769C>T r.(?) p.(Arg1257Cys)
?/. - c.4246G>A r.(?) p.(Ala1416Thr)
?/. - c.4261G>A r.(?) p.(Ala1421Thr)
-/. - c.4383C>T r.(?) p.(Thr1461=)
-?/. - c.4567G>A r.(?) p.(Ala1523Thr)
-?/. - c.4572C>T r.(?) p.(Arg1524=)
-?/. - c.4701G>A r.(?) p.(Pro1567=)
?/. - c.4714+316C>T r.(=) p.(=)
?/. - c.4714+481A>C r.(=) p.(=)
?/. - c.4714+481A>C r.(=) p.(=)
-?/. - c.4758G>A r.(?) p.(Thr1586=)
?/. - c.4787C>T r.(?) p.(Pro1596Leu)
-?/. - c.4842G>A r.(?) p.(Leu1614=)
?/. - c.5148C>T r.(?) p.(Arg1716=)
-?/. - c.5459C>T r.(?) p.(Thr1820Met)
?/. - c.5500_5517dup r.(?) p.(Ser1834_Gly1839dup)
?/. - c.5626C>T r.(?) p.(His1876Tyr)
-?/. - c.5688-7C>T r.(=) p.(=)
-?/. - c.5798T>C r.(?) p.(Val1933Ala)
-?/. - c.6047C>T r.(?) p.(Ser2016Leu)
?/. - c.6251G>A r.(?) p.(Arg2084Gln)
-?/. - c.6411+9G>A r.(=) p.(=)
?/. - c.6455T>C r.(?) p.(Leu2152Pro)
-?/. - c.6495G>A r.(?) p.(Gly2165=)
-?/. - c.6546C>A r.(?) p.(Leu2182=)
?/. - c.6704G>A r.(?) p.(Arg2235Gln)
?/. - c.6887G>A r.(?) p.(Arg2296Gln)
?/. - c.6910A>G r.(?) p.(Ser2304Gly)
-?/. - c.7263G>T r.(?) p.(=)
?/. - c.7334G>A r.(?) p.(Arg2445His)
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