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

95 entries on 1 page. Showing entries 1 - 95.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - 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.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.370G>A r.(?) p.(Val124Ile)
-?/. - c.416A>C r.(?) p.(Glu139Ala)
+/. - c.615_618del r.(?) p.(Lys206Profs*15)
+?/. - c.615_618del r.(?) p.(Lys206Profs*15)
+?/. - c.615_618del r.(?) p.(Lys206Profs*15)
?/. - c.638G>A r.(?) p.(Arg213His)
+?/. - 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.782-2A>G r.spl? p.(Val262_Gly318del)
+?/. - c.782-2A>T r.spl p.?
+?/. - c.782-1G>T r.spl 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.881A>C r.(?) p.(His294Pro)
./. - c.881A>C r.(?) p.(His294Pro)
+?/. - c.886T>G r.(?) p.(Cys296Gly)
+?/. - c.952G>C r.(?) p.(Gly318Arg)
+?/. - c.979T>A r.(?) p.(Cys327Ser)
+?/. - 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.1024C>T r.(?) p.(Arg342Cys)
+?/. - c.1024C>T r.(?) p.(Arg342Cys)
+?/. - c.1025G>A r.(?) p.(Arg342His)
+?/. - c.1025G>A r.(?) p.(Arg342His)
+?/. - c.1029C>G r.(?) p.(Tyr343Ter)
+?/. 5 c.1033C>T r.(?) p.(His345Tyr)
?/. - c.1042G>A r.(?) p.(Glu348Lys)
+?/. - c.1078A>C r.(?) p.(Ser360Arg)
-?/. - c.1086+10C>G r.(=) p.(=)
./. - 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.1117C>G r.(?) p.(His373Asp)
?/. - c.1118A>C r.(?) p.(His373Pro)
+?/. - c.1118A>C r.(?) p.(His373Pro)
?/. - c.1120A>G r.(?) p.(Thr374Ala)
+/. - c.1130G>A r.(?) p.(Arg377His)
+?/. - c.1130G>A r.(?) p.(Arg377His)
+?/. - c.1130G>A r.(?) p.(Arg377His)
./. - c.1133C>T r.(?) p.(Pro378Leu)
+?/. - c.1133C>T r.(?) p.(Pro378Leu)
+?/. - c.1133C>T r.(?) p.(Pro378Leu)
+?/. - c.1168G>A r.(?) p.(Asp390Asn)
+?/. 6 c.1169A>G r.(1169A>G) p.(Asp390Gly)
+?/. - c.1226G>A r.(?) p.(Cys409Tyr)
-?/. - c.1243C>T r.(?) p.(Arg415Trp)
?/. - c.1336A>G r.(?) p.(Ile446Val)
+?/. - c.1342C>T r.(?) p.(Arg448Ter)
+?/. - c.1343G>A r.(?) p.(Arg448Gln)
+?/. - c.1343G>A r.(?) p.(Arg448Gln)
+?/. - c.1357+2201_1518+520del r.(?) p.(Val454Glufs*23)
+?/. - c.1418A>G r.(?) p.(Asp473Gly)
+/. - c.1454A>G r.(?) p.(His485Arg)
-?/. - c.1519-699G>A r.(=) p.(=)
+/. - c.1531dup r.(?) p.(Ile511Asnfs*20)
?/. - c.1543C>T r.(?) p.(Arg515Cys)
+?/. - c.1568dup r.(?) p.(Tyr523*)
?/. - c.1585G>A r.(?) p.(Asp529Asn)
?/. - c.1585G>A r.(?) p.(Asp529Asn)
?/. - c.1586A>G r.(?) p.(Asp529Gly)
+?/. - c.1670_1674del r.(?) p.(Cys557*)
+?/. - c.1699C>T r.(?) p.(Arg567Trp)
-?/. - c.1702-216G>A r.(=) p.(=)
-/. - c.1702-10T>C r.(=) p.(=)
-?/. - c.1747G>A r.(?) p.(Val583Ile)
-?/. - c.1755G>A r.(?) p.(Gly585=)
-?/. - c.1860C>T r.(?) p.(Asp620=)
?/. 11 c.1883C>T r.(?) p.(Pro628Leu)
?/. - c.1918C>T r.(?) p.(Pro640Ser)
-?/. - c.1927C>T r.(?) p.(Pro643Ser)
-?/. - c.1927C>T r.(?) p.(Pro643Ser)
+?/. - c.1960C>T r.(?) p.(Arg654*)
-?/. - c.2116C>T r.(?) p.(Pro706Ser)
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