Transcript #00001231 (NM_014141.5, CNTNAP2 gene)

Transcript name contactin associated protein-like 2
Gene name CNTNAP2 (contactin associated protein-like 2)
Chromosome 7
Transcript - NCBI ID NM_014141.5
Transcript - Ensembl ID -
Protein - NCBI ID NP_054860.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-09-13 13:20:16 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. 9i_10i c.(1498+1_1499-1)_(1670+1_1671_1)del r.? p.?
?/. - c.73G>A r.(?) p.(Ala25Thr)
?/. - c.73G>A r.(?) p.(Ala25Thr)
?/. - c.73G>A r.(?) p.(Ala25Thr)
-/. - c.73G>A r.(?) p.(Ala25Thr)
-?/. - c.90C>T r.(?) p.(Ser30=)
?/. - c.97C>G r.(?) p.(Gln33Glu)
+/. 1i_3i c.(97+1_97+262659)_(98-148420_403-1)del r.? p.?
+?/. 1i_2i c.(97+1_98-1)_(208+1_209-1)dup r.? p.?
?/. - c.275G>A r.(?) p.(Arg92Gln)
-/. - c.318C>T r.(?) p.(Ser106=)
?/. - c.400T>G r.(?) p.(Trp134Gly)
-/. - c.402+8A>G r.(=) p.(=)
?/. - c.416A>G r.(?) p.(Asn139Ser)
?/. - c.416A>G r.(?) p.(Asn139Ser)
?/. - c.479G>A r.(?) p.(Arg160His)
?/. - c.479G>A r.(?) p.(Arg160His)
./. - c.479G>A r.(?) p.(Arg160His)
?/. - c.511C>T r.(?) p.(Arg171Cys)
?/. - c.542G>T r.(?) p.(Cys181Phe)
+/. - c.549del r.(?) p.(Trp184GlyfsTer22)
-?/. - c.551-11T>G r.(=) p.(=)
-/. - c.551-11_551-10insG r.(=) p.(=)
-/. - c.551-11_551-10insG r.(=) p.(=)
-/. - c.551-11_551-10insG r.(=) p.(=)
-/. - c.551-8del r.(=) p.(=)
-?/. - c.551-7G>T r.(=) p.(=)
-?/. - c.551-7G>T r.(=) p.(=)
-?/. - c.580G>A r.(?) p.(Val194Ile)
-/. - c.632T>C r.(?) p.(Val211Ala)
-?/. - c.681C>A r.(?) p.(His227Gln)
-?/. - c.681C>T r.(?) p.(His227=)
-?/. - c.681C>T r.(?) p.(His227=)
-?/. - c.718C>T r.(?) p.(Leu240=)
./. - c.755-5C>T r.spl? p.?
-?/. - c.837G>A r.(?) p.(Val279=)
?/. - c.854G>C r.(?) p.(Gly285Ala)
-?/. - c.854G>C r.(?) p.(Gly285Ala)
-?/. - c.860G>A r.(?) p.(Ser287Asn)
-?/. - c.924G>A r.(?) p.(Leu308=)
?/. - c.940-13C>A r.(=) p.(=)
?/. - c.1031G>T r.(?) p.(Gly344Val)
-?/. - c.1032C>T r.(?) p.(Gly344=)
-?/. - c.1083G>A r.(?) p.(Val361=)
-?/. - c.1083G>A r.(?) p.(Val361=)
?/. - c.1083G>A r.(?) p.(Val361=)
-?/. - c.1083G>A r.(?) p.(Val361=)
-/. - c.1119G>A r.(?) p.(Thr373=)
?/. - c.1135A>G r.(?) p.(Asn379Asp)
?/. 8 c.1157T>C r.(?) p.(Val386Ala)
?/. - c.1165C>T r.(?) p.(Arg389Trp)
-?/. - c.1220A>G r.(?) p.(Asn407Ser)
-?/. - c.1220A>G r.(?) p.(Asn407Ser)
-?/. - c.1220A>G r.(?) p.(Asn407Ser)
-?/. - c.1247C>T r.(?) p.(Ala416Val)
./. - c.1249G>T r.(?) p.(Asp417Tyr)
-?/. - c.1308C>T r.(?) p.(Asn436=)
-?/. - c.1311C>T r.(?) p.(Ile437=)
-/. - c.1311C>T r.(?) p.(Ile437=)
./. - c.1329_1330insTA r.(?) p.(Gln444Tyrfs*11)
-/. - c.1349-30T>A r.(=) p.(=)
./. - c.1406T>C r.(?) p.(Phe469Ser)
./. - c.1406T>C r.(?) p.(Phe469Ser)
./. - c.1406T>C r.(?) p.(Phe469Ser)
-?/. - c.1455T>C r.(?) p.(Asn485=)
-?/. - c.1597T>A r.(?) p.(Leu533Ile)
-?/. - c.1603G>A r.(?) p.(Glu535Lys)
-?/. - c.1603G>A r.(?) p.(Glu535Lys)
-/. - c.1659G>A r.(?) p.(Ala553=)
-/. - c.1659G>A r.(?) p.(Ala553=)
-/. - c.1659G>A r.(?) p.(Ala553=)
?/. - c.1671-7_1671-6dup r.(=) p.(=)
+/. - c.1671-1G>T r.spl? p.?
-/. - c.1710G>A r.(?) p.(Ser570=)
-?/. - c.1725C>T r.(?) p.(Ser575=)
+?/. - c.1777+5G>A r.spl? p.?
-?/. - c.1777+7G>A r.(=) p.(=)
-/. - c.1777+10A>G r.(=) p.(=)
-/. - c.1777+10A>G r.(=) p.(=)
-/. - c.1777+10A>G r.(=) p.(=)
-?/. - c.1777+13T>G r.(=) p.(=)
-?/. - c.1777+13T>G r.(=) p.(=)
?/. - c.1786G>A r.(?) p.(Glu596Lys)
-?/. - c.1854C>T r.(?) p.(Gly618=)
./. - c.1868G>A r.(?) p.(Gly623Glu)
-?/. - c.1897+8T>C r.(=) p.(=)
-/. - c.1897+25A>G r.(=) p.(=)
-?/. - c.1898-1_1903del r.spl? p.?
?/. - c.2038G>A r.(?) p.(Glu680Lys)
?/. - c.2047G>A r.(?) p.(Glu683Lys)
?/. - c.2098+5G>A r.spl? p.?
-/. - c.2099-15T>C r.(=) p.(=)
-/. - c.2099-15T>C r.(=) p.(=)
?/. - c.2123T>C r.(?) p.(Val708Ala)
./. - c.2147A>G r.(?) p.(Tyr716Cys)
+?/. - c.2148C>G r.(?) p.(Tyr716Ter)
+/. - c.2153G>A r.(?) p.(Trp718*)
./. - c.2206T>A r.(?) p.(Cys736Ser)
?/. - c.2206T>A r.(?) p.(Cys736Ser)
./. - c.2207G>A r.(?) p.(Cys736Tyr)
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