Transcript #00005834 (NM_006565.3, CTCF gene)

Transcript name transcript variant 1
Gene name CTCF (CCCTC-binding factor (zinc finger protein))
Chromosome 16
Transcript - NCBI ID NM_006565.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_006556.1
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.(?_-862850)_(*3162128_?)del r.0 p.0
+/. - c.(?_-848141)_(*1288279_?)del r.0 p.0
+/. - c.(?_-496754)_(*528225_?)del r.0 p.0
+/. - c.(?_-296754)_(*1228225_?)del r.0 p.0
+?/. - c.(?_-250903)_(*1227771_?)del r.0 p.0
+?/. - c.(?_-8478)_(*501684_?)del r.0? p.0?
-?/. - c.-10+3805G>T r.(=) p.(=)
-?/. - c.-10+10682G>A r.(=) p.(=)
-?/. - c.-9-2986T>C r.(=) p.(=)
?/. - c.-9-1G>A r.spl? p.?
+/. - c.-(?_195768)_(*6135_?)del r.0 p.0
?/. - c.10G>A r.(?) p.(Asp4Asn)
?/. - c.142G>T r.(?) p.(Gly48Cys)
+?/. - c.148dup r.(?) p.(Val50Glyfs*27)
+?/. - c.214C>T r.(?) p.(Gln72*)
?/. - c.232A>G r.(?) p.(Met78Val)
-?/. - c.236A>G r.(?) p.(Glu79Gly)
+/. - c.329dup r.(?) p.(Gly111ArgfsTer29)
?/. - c.370G>A r.(?) p.(Val124Ile)
+/. - c.375dup r.0 p.0
-?/. - c.416A>C r.(?) p.(Glu139Ala)
+/. - c.532_538del r.(?) p.(Leu178LysfsTer42)
+/. - c.615_618del r.(?) p.(Lys206ProfsTer15)
+/. - c.615_618del r.(?) p.(Lys206Profs*15)
+?/. - c.615_618del r.(?) p.(Lys206Profs*15)
+?/. - c.615_618del r.(?) p.(Lys206Profs*15)
+/. - c.615_618del r.(?) p.(Lys206ProfsTer15)
+/. - c.615_618del r.(?) p.(Lys206ProfsTer15)
+/. - c.615_618del r.(?) p.(Lys206ProfsTer15)
?/. - c.638G>A r.(?) p.(Arg213His)
+?/. - c.677A>G r.(?) p.(Tyr226Cys)
+?/. - c.688del r.(?) p.(Glu230Lysfs*20)
?/. - c.702G>T r.(?) p.(Glu234Asp)
-?/. - c.702G>T r.(?) p.(Glu234Asp)
-?/. - c.702G>T r.(?) p.(Glu234Asp)
?/. - c.707T>G r.(?) p.(Leu236Arg)
+?/. - c.773_776del r.(?) p.(Lys258Argfs*4)
+/. - c.778_781del r.(?) p.(Lys260ValfsTer2)
+?/. - c.782-2A>G r.spl? p.(Val262_Gly318del)
+?/. - c.782-2A>G r.(782_952del) p.(Val262_Gly318del)
+?/. - c.782-2A>T r.spl p.?
+?/. 3i c.782-1G>T r.782_952del p.Val262_Gly318del
?/. - c.791_793del r.(?) p.(Lys264del)
+/. - c.804_805del r.(?) p.(Cys268Ter)
+?/. - c.804_805del r.(?) p.(Cys268*)
?/. - c.833G>A r.(?) p.(Arg278His)
?/. - c.833G>T r.(?) p.(Arg278Leu)
+?/. - c.833G>T r.(?) p.(Arg278Leu)
+?/. - c.848G>A r.(?) p.(Arg283His)
+?/. - c.848G>A r.(?) p.(Arg283His)
+?/. - c.862C>T r.(?) p.(His288Tyr)
+?/. - c.881A>C r.(?) p.(His294Pro)
./. - c.881A>C r.(?) p.(His294Pro)
+?/. - c.886T>G r.(?) p.(Cys296Gly)
+/. - c.897_898del r.(?) p.(Cys299TrpfsTer15)
+?/. - c.934del r.(?) p.(His312ThrfsTer21)
+?/. - c.952G>C r.(?) p.(Gly318Arg)
+?/. 5 c.959G>A r.(?) p.(Arg320His)
+?/. - c.979T>A r.(?) p.(Cys327Ser)
+?/. - c.1003G>A r.(?) p.(Gly335Arg)
+/. - c.1004del r.(?) p.(Gly335GlufsTer27)
+?/. - c.1006G>C r.(?) p.(Glu336Gln)
+/. - c.1016G>A r.(?) p.(Arg339Gln)
+?/. - c.1016G>A r.(?) p.(Arg339Gln)
+/. - c.1016G>A r.(?) p.(Arg339Gln)
+/. - c.1016G>A r.(?) p.(Arg339Gln)
+?/. - c.1016G>A r.(?) p.(Arg339Gln)
+/. - c.1016G>A r.(?) p.(Arg339Gln)
+/. - c.1016G>A r.(?) p.(Arg339Gln)
+/. - c.1016G>A r.(?) p.(Arg339Gln)
?/. - c.1016G>A r.(?) p.(Arg339Gln)
+?/. - c.1024C>T r.(?) p.(Arg342Cys)
+?/. - c.1024C>T r.(?) p.(Arg342Cys)
+?/. - c.1024C>T r.(?) p.(Arg342Cys)
+?/. - c.1025G>A r.(?) p.(Arg342His)
+?/. - c.1025G>A r.(?) p.(Arg342His)
+?/. - c.1025G>A r.(?) p.(Arg342His)
+?/. - c.1025G>A r.(?) p.(Arg342His)
+?/. - c.1028A>G r.(?) p.(Tyr343Cys)
+/. - c.1029C>A r.(?) p.(Tyr343Ter)
?/. - c.1029C>A r.(?) p.(Tyr343Ter)
+?/. - c.1029C>G r.(?) p.(Tyr343Ter)
+?/. 5 c.1033C>T r.(?) p.(His345Tyr)
+/. - c.1039del r.(?) p.(His347ThrfsTer15)
?/. - c.1042G>A r.(?) p.(Glu348Lys)
+?/. - c.1078A>C r.(?) p.(Ser360Arg)
+?/. - c.1079G>A r.(?) p.(Ser360Asn)
+?/. - c.1079G>A r.(?) p.(Ser360Asn)
-?/. - c.1086+10C>G r.(=) p.(=)
+?/. - c.1094A>G r.(?) p.(Lys365Arg)
+/. - c.1102C>T r.(?) p.(Arg368Cys)
+?/. - c.1102C>T r.(?) p.(Arg368Cys)
./. - c.1102C>T r.(?) p.(Arg368Cys)
+?/. - c.1102C>T r.(?) p.(Arg368Cys)
+?/. - c.1102C>T r.(?) p.(Arg368Cys)
+/. - c.1102C>T r.(?) p.(Arg368Cys)
+?/. - c.1103G>A r.(?) p.(Arg368His)
+?/. - c.1103G>A r.(?) p.(Arg368His)
+?/. - c.1112G>C r.(?) p.(Arg371Pro)
?/. - c.1114T>C r.(?) p.(Ser372Pro)
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