Transcript #00005398 (NM_016284.4, CNOT1 gene)

Transcript name transcript variant 1
Gene name CNOT1 (CCR4-NOT transcription complex, subunit 1)
Chromosome 16
Transcript - NCBI ID NM_016284.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_057368.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.-333_*1012[0] r.0 p.0
?/. - c.36A>C r.(?) p.(Gln12His)
+/. - c.76C>T r.(?) p.(Arg26*)
+/. - c.76C>T r.(?) p.(Arg26*)
+/. - c.76C>T r.(?) p.(Arg26*)
+/. - c.76C>T r.(?) p.(Arg26*)
+/. - c.76C>T r.(?) p.(Arg26*)
+/. - c.97C>T r.(?) p.(Gln33*)
+/. - c.102+2T>C r.spl p.?
+/. - c.102+2T>C r.spl p.?
-?/. - c.102+1747C>G r.(=) p.(=)
?/. - c.112C>T r.(?) p.(Arg38Trp)
+/. - c.210+1G>T r.spl p.?
?/. - c.256A>G r.(?) p.(Asn86Asp)
?/. - c.278A>G r.(?) p.(Tyr93Cys)
?/. - c.292C>A r.(?) p.(Pro98Thr)
+?/. - c.378+1G>A r.spl? p.?
?/. - c.385T>C r.(?) p.(Phe129Leu)
?/. - c.467T>C r.(?) p.(Leu156Pro)
?/. - c.482T>C r.(?) p.(Ile161Thr)
-?/. - c.487G>A r.(?) p.(Ala163Thr)
-?/. - c.532A>G r.(?) p.(Ile178Val)
-?/. - c.560A>G r.(?) p.(His187Arg)
+/. - c.608_611del r.(?) p.(Ile203Thrfs*32)
-?/. - c.637+69T>C r.(=) p.(=)
-?/. - c.953G>T r.(?) p.(Ser318Ile)
-?/. - c.1105C>T r.(?) p.(Arg369Cys)
+/. - c.1188T>A r.(?) p.(Tyr396*)
?/. - c.1285del r.(?) p.(Val429Leufs*6)
?/. - c.1525A>G r.(?) p.(Ile509Val)
-?/. - c.1584+7T>A r.(=) p.(=)
+/. - c.1603C>T r.(?) p.(Arg535Cys)
+/. - c.1603C>T r.(?) p.(Arg535Cys)
+/. - c.1603C>T r.(?) p.(Arg535Cys)
+/. - c.1603C>T r.(?) p.(Arg535Cys)
+/. - c.1603C>T r.(?) p.(Arg535Cys)
+?/. - c.1603C>T r.(?) p.(Arg535Cys)
+/. - c.1603C>T r.(?) p.(Arg535Cys)
+/. - c.1603C>T r.(?) p.(Arg535Cys)
?/. - c.1643G>A r.(?) p.(Arg548Lys)
?/. - c.1771C>T r.(?) p.(Arg591Cys)
?/. - c.1787A>G r.(?) p.(Lys596Arg)
+/. - c.1924C>G r.(?) p.(Gln642Glu)
?/. - c.1951A>G r.(?) p.(Met651Val)
+/. 16i_21i c.(1979+1_1980-63)_(2891+21_2891-1)del r.? p.?
?/. - c.2255A>T r.(?) p.(Lys752Ile)
?/. - c.2320T>A r.(?) p.(Ser774Thr)
?/. - c.2413G>A r.(?) p.(Val805Ile)
-?/. - c.2480-5A>G r.spl? p.?
-?/. - c.2481G>A r.(?) p.(=)
+/. - c.2620C>T r.(?) p.(Gln874*)
+/. - c.2689G>A r.(?) p.(Glu897Lys)
+/. - c.2698C>T r.(?) p.(Arg900Cys)
-?/. - c.2891+445G>A r.(=) p.(=)
?/. - c.2891+493C>T r.(=) p.(=)
-?/. - c.3065_3076dup r.(?) p.(Ala1022_Gln1025dup)
?/. - c.3113C>T r.(?) p.(Thr1038Ile)
?/. - c.3152C>T r.(?) p.(Thr1051Met)
-?/. - c.3202-3dup r.spl? p.?
+?/. - c.3265G>C r.(?) p.(Val1089Leu)
?/. - c.3362C>T r.(?) p.(Thr1121Met)
+/. - c.3363_3364insTAAGGTAAGCTAAA r.(?) p.(Val1122*)
+?/. - c.3443T>C r.(?) p.(Leu1148Pro)
+/. - c.3443T>C r.(?) p.(Leu1148Pro)
+/. - c.3563A>G r.(?) p.(Asp1188Gly)
-?/. - c.3625C>A r.(?) p.(Pro1209Thr)
?/. - c.3634C>G r.(?) p.(His1212Asp)
+/. - c.3681_3687del r.(?) p.(Lys1227Asnfs*7)
+/. - c.3722A>G r.(?) p.(Lys1241Arg)
+/. - c.3750+1G>T r.spl p.?
+/. - c.3750+5G>A r.spl? p.?
+?/. I27 c.3750+5G>A r.spl? p.?
-?/. - c.4021C>T r.(?) p.(Pro1341Ser)
+/. - c.4138-2A>C r.spl p.?
+/. - c.4255A>G r.(?) p.(Thr1419Ala)
+/. - c.4283T>C r.(?) p.(Phe1428Ser)
?/. - c.4283T>C r.(?) p.(Phe1428Ser)
?/. - c.4336C>T r.(?) p.(Arg1446Cys)
?/. - c.4399A>G r.(?) p.(Thr1467Ala)
+/. - c.4432C>T r.(?) p.(Arg1478Cys)
-?/. - c.4434+44G>C r.(=) p.(=)
-?/. - c.4434+70_4434+73del r.(=) p.(=)
-?/. - c.4434+182del r.(=) p.(=)
-?/. - c.4434+194_4434+195del r.(=) p.(=)
-/. - c.4434+195del r.(=) p.(=)
-/. - c.4434+195dup r.(=) p.(=)
+/. - c.4482A>T r.(?) p.(Gln1494His)
+/. - c.4714T>G r.(?) p.(Tyr1572Asp)
-?/. - c.4733A>G r.(?) p.(Asn1578Ser)
-?/. - c.4733A>G r.(?) p.(Asn1578Ser)
+/. - c.4800G>C r.(?) p.(Lys1600Asn)
+/. - c.4800+1G>A r.spl p.?
?/. - c.4876A>G r.(?) p.(Ile1626Val)
-?/. - c.5107T>G r.(?) p.(Ser1703Ala)
?/. - c.5201A>G r.(?) p.(Asn1734Ser)
-?/. - c.5331T>G r.(?) p.(=)
?/. - c.5468G>A r.(?) p.(Arg1823His)
+?/. - c.5536C>G r.(?) p.(Pro1846Ala)
?/. 39 c.5608C>T r.(?) p.(Arg1870Cys)
?/. - c.6095C>G r.(?) p.(Pro2032Arg)
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