Transcript #00014368 (NM_006311.3, NCOR1 gene)

Transcript name transcript variant 1
Gene name NCOR1 (nuclear receptor corepressor 1)
Chromosome 17
Transcript - NCBI ID NM_006311.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_006302.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

62 entries on 1 page. Showing entries 1 - 62.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-2174C>T r.(?) p.(=)
?/. - c.-2078G>A r.(?) p.(=)
?/. - c.-70G>A r.(=) p.(=)
?/. - c.97C>T r.(?) p.(Arg33Cys)
-?/. - c.148G>A r.(?) p.(Val50Met)
?/. - c.277C>G r.(?) p.(His93Asp)
-?/. - c.310C>G r.(?) p.(Leu104Val)
?/. - c.360G>T r.(?) p.(Gln120His)
?/. - c.540G>C r.(?) p.(Glu180Asp)
-?/. - c.621A>G r.(?) p.(Gln207=)
?/. - c.1274A>T r.(?) p.(Glu425Val)
+?/. - c.1451dup r.(?) p.(Asn484LysfsTer2)
?/. - c.1549_1551del r.(?) p.(Lys517del)
-?/. - c.1582_1584del r.(?) p.(Lys528del)
?/. - c.1646A>G r.(?) p.(Lys549Arg)
?/. - c.2338G>A r.(?) p.(Val780Met)
-?/. - c.2549G>A r.(?) p.(Ser850Asn)
-?/. - c.2690+9C>T r.(=) p.(=)
-?/. - c.2707T>C r.(?) p.(Ser903Pro)
?/. - c.3253T>G r.(?) p.(Ser1085Ala)
-?/. - c.3338G>A r.(?) p.(Arg1113Gln)
?/. - c.3360G>C r.(?) p.(Glu1120Asp)
-?/. - c.3406G>A r.(?) p.(Ala1136Thr)
?/. - c.3710C>T r.(?) p.(Thr1237Ile)
?/. - c.4173C>G r.(?) p.(Asp1391Glu)
-?/. - c.4243C>T r.(?) p.(Arg1415Cys)
-?/. - c.4244G>A r.(?) p.(Arg1415His)
?/. - c.4324G>A r.(?) p.(Glu1442Lys)
-?/. - c.4471A>G r.(?) p.(Thr1491Ala)
-?/. - c.4476G>A r.(?) p.(Met1492Ile)
-/. - c.4863A>G r.(?) p.(=)
?/. - c.5146C>T r.(?) p.(Arg1716Trp)
?/. - c.5151_5156del r.(?) p.(Arg1720_Glu1721del)
?/. - c.5163_5180dup r.(?) p.(Lys1722_Glu1727dup)
?/. - c.5175_5180dup r.(?) p.(Glu1727_Arg1728dup)
?/. - c.5240G>A r.(?) p.(Arg1747Gln)
-?/. - c.5632G>A r.(?) p.(Val1878Ile)
-?/. - c.5859A>C r.(?) p.(Gln1953His)
-?/. - c.5975A>G r.(?) p.(Tyr1992Cys)
-?/. - c.6010+6T>C r.(=) p.(=)
?/. - c.6053G>T r.(?) p.(Arg2018Leu)
?/. - c.6214A>C r.(?) p.(Thr2072Pro)
-?/. - c.6536G>A r.(?) p.(Arg2179Lys)
?/. - c.6641G>A r.(?) p.(Arg2214His)
-?/. - c.6754C>T r.(?) p.(His2252Tyr)
?/. - c.6773C>G r.(?) p.(Ala2258Gly)
-?/. - c.6901G>T r.(?) p.(Val2301Phe)
?/. - c.6955+4C>T r.spl? p.?
-?/. - c.6957A>G r.(?) p.(=)
-?/. - c.7034T>C r.(?) p.(Leu2345Ser)
?/. - c.*4801T>C r.(=) p.(=)
+/. - c.*4809_*4813del r.(=) p.(=)
?/. - c.*4845G>A r.(=) p.(=)
-?/. - c.*4876T>C r.(=) p.(=)
+/. - c.*4911G>A r.(=) p.(=)
?/. - c.*4920G>A r.(=) p.(=)
-?/. - c.*5611G>A r.(=) p.(=)
-?/. - c.*5682C>T r.(=) p.(=)
?/. - c.*5683A>G r.(=) p.(=)
-?/. - c.*5690T>G r.(=) p.(=)
?/. - c.*7136T>C r.(=) p.(=)
?/. - c.*7169C>A r.(=) p.(=)
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