Transcript #00000264 (NM_030653.3, DDX11 gene)

Transcript name DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 11, transcript variant 1
Gene name DDX11 (DEAD/H (Asp-Glu-Ala-Asp/His) box helicase 11)
Chromosome 12
Transcript - NCBI ID NM_030653.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_085911.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-08-01 11:29:47 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-5+20C>T r.(=) p.(=)
-?/. - c.147G>A r.(?) p.(Gly49=)
-/. - c.147G>A r.(?) p.(Gly49=)
?/. - c.167G>T r.(?) p.(Cys56Phe)
+/. - c.169G>C r.(?) p.(Gly57Arg)
-?/. - c.254A>G r.(?) p.(His85Arg)
-?/. - c.254A>G r.(?) p.(His85Arg)
-?/. - c.394-7C>T r.(=) p.(=)
?/. - c.395C>T r.(?) p.(Ala132Val)
?/. - c.419G>A r.(?) p.(Arg140Gln)
+?/. 4 c.419G>A r.419g>a p.Arg140Gln
?/. - c.482G>T r.(?) p.(Arg161Met)
-?/. - c.499A>G r.(?) p.(Arg167Gly)
+/. - c.606del r.(?) p.(Tyr202Ter)
-?/. - c.611G>A r.(?) p.(Ser204Asn)
-?/. - c.637A>G r.(?) p.(Arg213Gly)
+/. - c.638+1G>A r.spl p.?
-/. - c.638+15G>A r.(=) p.(=)
-/. - c.638+886A>G r.(=) p.(=)
-/. - c.639-10A>T r.(=) p.(=)
-?/. - c.639-6A>T r.(=) p.(=)
-?/. - c.639-4A>C r.spl? p.?
+/. 7 c.788G>A r.(?) p.(Arg263Gln)
+/. 7 c.788G>A r.(?) p.(Arg263Gln)
+/. 7 c.788G>A r.(?) p.(Arg263Gln)
?/. - c.788G>A r.(?) p.(Arg263Gln)
-?/. - c.793-8T>C r.(=) p.(=)
-/. - c.814G>A r.(?) p.(Val272Met)
-/. - c.818A>G r.(?) p.(Lys273Arg)
-?/. - c.906G>A r.(?) p.(Glu302=)
+/. - c.907_920del r.(?) p.(Lys303GlufsTer22)
+/. - c.907_920del r.(?) p.(Lys303GlufsTer22)
-?/. - c.916A>C r.(?) p.(=)
-/. - c.923_925dup r.(?) p.(Arg308dup)
-?/. - c.930G>A r.(?) p.(Glu310=)
-/. - c.1060G>A r.(?) p.(Gly354Arg)
?/. - c.1093G>A r.(?) p.(Val365Met)
?/. - c.1102C>T r.(?) p.(Pro368Ser)
-?/. - c.1102C>T r.(?) p.(Pro368Ser)
?/. - c.1106A>G r.(?) p.(Tyr369Cys)
?/. - c.1106A>G r.(?) p.(Tyr369Cys)
?/. - c.1129A>G r.(?) p.(Thr377Ala)
?/. - c.1130C>T r.(?) p.(Thr377Ile)
+/. - c.1133G>C r.(?) p.(Arg378Pro)
-/. - c.1140C>T r.(?) p.(Ala380=)
?/. - c.1177G>A r.(?) p.(Asp393Asn)
?/. - c.1177G>A r.(?) p.(Asp393Asn)
?/. - c.1211G>T r.(?) p.(Gly404Val)
?/. 10 c.1221C>A r.(?) p.(Ser407Arg)
?/. - c.1221C>A r.(?) p.(Ser407Arg)
-?/. - c.1221C>T r.(?) p.(Ser407=)
-?/. - c.1242+4T>C r.spl? p.?
-?/. - c.1242+4T>C r.spl? p.?
-?/. - c.1283G>A r.(?) p.(Arg428Gln)
-?/. - c.1290-16_1312del r.spl? p.?
?/. - c.1341G>T r.(?) p.(Leu447Phe)
?/. - c.1376T>A r.(?) p.(Ile459Asn)
+/. - c.1403dup r.(?) p.(Ser469Valfs*32)
+?/. - c.1403dup r.(?) p.(Ser469Valfs*32)
+?/. 13 c.1403dup r.1403dup p.Ser469Valfs*32
-?/. - c.1415-7T>C r.(=) p.(=)
-/. - c.1415-7T>C r.(=) p.(=)
?/. - c.1438G>A r.(?) p.(Asp480Asn)
?/. - c.1439A>G r.(?) p.(Asp480Gly)
?/. - c.1466A>T r.(?) p.(Asn489Ile)
+/. - c.1523T>G r.(?) p.(Leu508Arg)
+/. - c.1523T>G r.(?) p.(Leu508Arg)
-?/. - c.1562C>T r.(?) p.(Ser521Phe)
-?/. - c.1657C>G r.(?) p.(Gln553Glu)
-?/. - c.1657C>G r.(?) p.(Gln553Glu)
+?/. 17 c.1672C>T r.(?) p.(Arg558*)
+/. - c.1672C>T r.(?) p.(Arg558Ter)
+?/. 17 c.1672C>T r.(?) p.(Arg558*)
-?/. - c.1693C>T r.(?) p.(His565Tyr)
-?/. - c.1696A>G r.(?) p.(Ile566Val)
-/. - c.1698C>T r.(?) p.(Ile566=)
-/. - c.1699C>G r.(?) p.(Gln567Glu)
+/. - c.1763-1G>C r.1763_1766del p.?
+/. - c.1763-1G>C r.1763_1766del p.?
+/. - c.1763-1G>C r.spl p.?
+/. - c.1763-1G>C r.spl p.?
+/. - c.1763-1G>C r.spl? p.?
+?/. - c.1763-1G>C r.spl? p.?
?/. 18 c.1774C>G r.(?) p.(Gln592Glu)
-/. - c.1819G>C r.(?) p.(Ala607Pro)
-?/. - c.1876-6C>T r.(=) p.(=)
+/. - c.1888del r.(?) p.(Arg630Glyfs*23)
-?/. - c.1916T>C r.(?) p.(Val639Ala)
?/. - c.1930G>A r.(?) p.(Val644Met)
?/. - c.1930G>A r.(?) p.(Val644Met)
+?/. 19 c.1930G>A r.1930g>a p.Val644Met
+/. - c.1948+1_1948+3del r.spl? p.(Gly650del)
+/. - c.1948+1_1948+3del r.spl? p.(Gly650del)
?/. - c.1948+1_1948+3del r.spl? p.?
+/. - c.1949-1G>A r.spl p.?
+/. - c.1949-1G>A r.spl p.?
-/. - c.1983C>T r.(?) p.(Leu661=)
-/. - c.2053-15C>T r.(=) p.(=)
?/. - c.2076C>T r.(?) p.(Leu692=)
+?/. 21 c.2114G>A r.2114g>a p.Cys705Tyr
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