Transcript #00024301 (NM_001006657.1, WDR35 gene)

Transcript name transcript variant 1
Gene name WDR35 (WD repeat domain 35)
Chromosome 2
Transcript - NCBI ID NM_001006657.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001006658.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2017-07-27 15:54:54 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-3100G>A r.(?) p.(=)
+?/+ 1 c.3G>A r.(?) p.(Met1_Ala30delinsMetfs*4)
+/. - c.25-2A>G r.spl? p.?
+/. - c.25-2A>G r.spl? p.?
-/. - c.53A>G r.(?) p.(Gln18Arg)
-/. - c.53A>G r.(?) p.(Gln18Arg)
+?/. 3 c.206G>A r.(?) p.(Gly69Asp)
+/. - c.206G>A r.(?) p.(Gly69Asp)
+?/. - c.215-8T>G r.214_215ins215-7_215-1 p.Val74Argfs*10
?/. - c.286A>C r.(?) p.(Ile96Leu)
+?/. 5 c.308G>T r.(?) p.(Gly103Val)
-?/. - c.309C>T r.(?) p.(Gly103=)
?/. - c.323A>C r.(?) p.(Glu108Ala)
+?/. 5 c.337C>T r.(?) p.(Arg113*)
-?/. - c.355C>T r.(?) p.(Arg119Cys)
?/. - c.355C>T r.(?) p.(Arg119Cys)
?/. - c.407A>T r.(?) p.(Asp136Val)
-?/. - c.437-13T>C r.(=) p.(=)
?/. - c.497C>A r.(?) p.(Ala166Glu)
-/. - c.549C>T r.(?) p.(Tyr183=)
-/. - c.549C>T r.(?) p.(Tyr183=)
+?/. 7 c.622G>C r.(?) p.(Ala208Pro)
-?/. - c.657C>T r.(?) p.(Tyr219=)
-?/. - c.761T>C r.(?) p.(Met254Thr)
-?/. - c.770T>C r.(?) p.(Val257Ala)
-?/. - c.770T>C r.(?) p.(Val257Ala)
-?/. - c.770T>C r.(?) p.(Val257Ala)
-?/. - c.853A>T r.(?) p.(Ile285Phe)
-?/. - c.853A>T r.(?) p.(Ile285Phe)
-?/. - c.853A>T r.(?) p.(Ile285Phe)
?/. - c.932G>T r.(?) p.(Trp311Leu)
+/. 9 c.932G>T r.(?) p.(Trp311Leu)
+/. - c.932G>T r.(?) p.(Trp311Leu)
-?/. - c.989A>G r.(?) p.(Asn330Ser)
-?/. - c.1058G>C r.(?) p.(Arg353Pro)
?/. - c.1081T>C r.(?) p.(Trp361Arg)
-/. - c.1089G>A r.(?) p.(Thr363=)
-?/. - c.1089G>A r.(?) p.(Thr363=)
-?/. - c.1183A>T r.(?) p.(Asn395Tyr)
?/. - c.1183A>T r.(?) p.(Asn395Tyr)
+?/. 10 c.1183A>T r.(?) p.(Asn395Tyr)
-?/. - c.1215A>G r.(?) p.(Thr405=)
-?/. - c.1226C>T r.(?) p.(Thr409Met)
-?/. - c.1335G>A r.(?) p.(Ser445=)
?/. - c.1363C>T r.(?) p.(Arg455Cys)
-?/. - c.1409G>A r.(?) p.(Arg470Gln)
+/. - c.1432_1433del r.(?) p.(Arg478Asnfs*5)
+/. - c.1433G>A r.(?) p.(Arg478Lys)
+/. 13i c.1433+3A>G r.spl? p.?
?/. - c.1475G>A r.(?) p.(Gly492Asp)
?/. - c.1486dup r.(?) p.(Tyr496Leufs*2)
+/. - c.1501del r.(?) p.(Gln501Lysfs*10)
-?/. - c.1503+7G>T r.(=) p.(=)
-?/. - c.1504-7A>G r.(=) p.(=)
?/. - c.1552A>T r.(?) p.(Ile518Phe)
-?/. - c.1557+3A>G r.spl? p.?
-?/. - c.1557+11C>A r.(=) p.(=)
-?/. - c.1557+11C>A r.(=) p.(=)
+/. - c.1579C>T r.(?) p.(Gln527*)
+?/. 16 c.1633C>T r.(?) p.(Arg545*)
-?/. - c.1634G>A r.(?) p.(Arg545Gln)
?/. - c.1634G>A r.(?) p.(Arg545Gln)
-/. - c.1634G>A r.(?) p.(Arg545Gln)
?/. - c.1670G>A r.(?) p.(Arg557His)
?/. - c.1694G>T r.(?) p.(Gly565Val)
-?/. - c.1788C>T r.(?) p.(Val596=)
+/. - c.1803G>A r.(?) p.(Trp601*)
-?/. - c.1879-19T>G r.(=) p.(=)
-?/. - c.1879-11del r.(=) p.(=)
?/. - c.1903A>T r.(?) p.(Ile635Phe)
+/. - c.1922T>G r.(?) p.(Leu641Ter)
+/. - c.1922T>G r.(?) p.(Leu641Ter)
+/. 18 c.1922T>G r.(?) p.(Leu641*)
+/. 18 c.1922T>G r.(?) p.(Leu641*)
+?/+? 18 c.1922T>G r.(?) p.(Leu641*)
+?/+? 18 c.1922T>G r.(?) p.(Leu641*)
+?/+? 18 c.1922T>G r.(?) p.(Leu641*)
+?/+? 18 c.1922T>G r.(?) p.(Leu641*)
?/. - c.1970A>G r.(?) p.(His657Arg)
+?/. - c.2096+1G>A r.spl? p.?
?/. - c.2098C>T r.(?) p.(Arg700Cys)
?/. - c.2099G>A r.(?) p.(Arg700His)
+?/. 20 c.2134del r.(?) p.(Leu712Tyrfs*20)
-?/. - c.2168A>G r.(?) p.(Lys723Arg)
-?/. - c.2182A>G r.(?) p.(Ile728Val)
?/. - c.2412T>G r.(?) p.(Asn804Lys)
-?/. - c.2447+20C>T r.(=) p.(=)
?/. - c.2491C>T r.(?) p.(Arg831Cys)
+?/+? 22 c.2522A>T r.(?) p.(Asp841Val)
+?/. 22 c.2522A>T r.(?) p.(Asp841Val)
+/. 22 c.2522A>T r.(?) p.(Asp841Val)
+/. 22 c.2522A>T r.(?) p.(Asp841Val)
+?/+? 22 c.2522A>T r.(?) p.(Asp841Val)
+?/+? 22 c.2522A>T r.(?) p.(Asp841Val)
+?/+? 22 c.2522A>T r.(?) p.(Asp841Val)
+?/+? 22 c.2522A>T r.(?) p.(Asp841Val)
-/. - c.2529A>G r.(?) p.(Glu843=)
-/. - c.2529A>G r.(?) p.(Glu843=)
-?/. - c.2557C>T r.(?) p.(Pro853Ser)
+/. - c.2623G>A r.(?) p.(Ala875Thr)
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