Transcript #00024068 (NM_001143992.1, WRAP53 gene)

Transcript name transcript variant 4
Gene name WRAP53 (WD repeat containing, antisense to TP53)
Chromosome 17
Transcript - NCBI ID NM_001143992.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001137464.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2015-10-26 21:19:59 +01:00 (CET)
Date last edited N/A


Variants

59 entries on 1 page. Showing entries 1 - 59.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. _1 c.-159G>C r.(=) p.(=)
-?/. - c.31C>T r.(?) p.(Pro11Ser)
?/. - c.106G>A r.(?) p.(Ala36Thr)
-?/. - c.187G>A r.(?) p.(Val63Met)
-/. - c.202C>G r.(?) p.(Arg68Gly)
?/. - c.208G>T r.(?) p.(Gly70Trp)
-?/. - c.395C>A r.(?) p.(Thr132Asn)
-?/. - c.407C>G r.(?) p.(Pro136Arg)
-?/. - c.431+15C>T r.(=) p.(=)
-/. - c.450C>T r.(?) p.(Phe150=)
?/. - c.487G>C r.(?) p.(Glu163Gln)
+/. 2 c.492C>A r.(?) p.(Phe164Leu)
-?/. - c.552C>T r.(?) p.(Ile184=)
-?/. - c.552C>T r.(?) p.(Ile184=)
?/. - c.656G>A r.(?) p.(Arg219Gln)
-?/. - c.720A>G r.(?) p.(Pro240=)
?/. - c.724A>G r.(?) p.(Thr242Ala)
?/. - c.725C>T r.(?) p.(Thr242Ile)
-?/. - c.747C>T r.(?) p.(Ser249=)
-?/. - c.822+6G>A r.(=) p.(=)
-?/. - c.823-10C>T r.(=) p.(=)
-?/. - c.823-10C>T r.(=) p.(=)
?/. - c.914C>T r.(?) p.(Thr305Met)
?/. - c.919C>T r.(?) p.(Arg307Trp)
?/. - c.919C>T r.(?) p.(Arg307Trp)
?/. - c.929G>A r.(?) p.(Arg310Gln)
-/. - c.936C>T r.(?) p.(Cys312=)
-/. - c.936C>T r.(?) p.(Cys312=)
./. - c.1024T>C r.(?) p.(Cys342Arg)
?/. - c.1034A>G r.(?) p.(Tyr345Cys)
+/. 8 c.1126C>T r.(?) p.(His376Tyr)
?/. - c.1132G>A r.(?) p.(Asp378Asn)
+?/. - c.1159C>T r.(?) p.(Arg387Cys)
?/. - c.1175T>A r.(?) p.(Leu392His)
+/. 9 c.1192C>T r.(?) p.(Arg398Trp)
-/. - c.1223G>A r.(?) p.(Gly408Asp)
+/. 10 c.1303G>A r.(?) p.(Gly435Arg)
?/. - c.1303G>A r.(?) p.(Gly435Arg)
-?/. - c.1308T>C r.(?) p.(Ala436=)
-?/. - c.1308T>C r.(?) p.(Ala436=)
?/. - c.1315G>A r.(?) p.(Val439Met)
?/. - c.1447C>T r.(?) p.(Arg483Cys)
-/. - c.1482A>G r.(?) p.(Glu494=)
-?/. - c.1493T>C r.(?) p.(Leu498Pro)
-?/. - c.1493T>C r.(?) p.(Leu498Pro)
-?/. - c.1514C>T r.(?) p.(Thr505Met)
-?/. - c.1537C>G r.(?) p.(Arg513Gly)
?/. - c.1537C>G r.(?) p.(Arg513Gly)
+/. - c.1564del r.(?) p.(Ala522Argfs*26)
?/. - c.1564dup r.(?) p.(Ala522Glyfs*8)
?/. - c.1564dup r.(?) p.(Ala522Glyfs*8)
-/. - c.1565C>G r.(?) p.(Ala522Gly)
-/. - c.1565C>G r.(?) p.(Ala522Gly)
-?/. - c.1565C>T r.(?) p.(Ala522Val)
-?/. - c.1566G>A r.(?) p.(Ala522=)
-?/. - c.1566G>A r.(?) p.(Ala522=)
-?/. - c.1566G>A r.(?) p.(Ala522=)
-?/. - c.1590T>A r.(?) p.(Asp530Glu)
-/. - c.1641G>T r.(?) p.(Leu547=)
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