Transcript #00022759 (NM_052844.3, WDR34 gene)

Transcript name WD repeat domain 34
Gene name WDR34 (WD repeat domain 34)
Chromosome 9
Transcript - NCBI ID NM_052844.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_443076.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

243 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.65C>T r.(?) p.(Ala22Val)
-?/. - c.100C>T r.(?) p.(Arg34Trp)
-/. - c.187-3C>A r.spl? p.?
-?/. - c.187-3C>A r.spl? p.?
-?/. - c.352A>C r.(?) p.(Met118Leu)
+/. 3 c.544C>T r.(?) p.(Arg182Trp)
?/. - c.565A>G r.(?) p.(Ser189Gly)
?/. - c.568A>G r.(?) p.(Thr190Ala)
?/. - c.583G>A r.(?) p.(Val195Met)
?/. - c.604C>T r.(?) p.(Arg202Trp)
-/. - c.616C>T r.(?) p.(Arg206Cys)
-?/. - c.632C>T r.(?) p.(Ser211Leu)
?/. - c.655G>A r.(?) p.(Ala219Thr)
?/. - c.782C>T r.(?) p.(Thr261Met)
+/. 6 c.935T>C r.(?) p.(Phe312Ser)
?/. 6 c.967A>C r.(?) p.(Thr323Pro)
-?/. - c.981+4C>T r.spl? p.?
?/. - c.988C>T r.(?) p.(Arg330Cys)
?/. - c.1008C>T r.(?) p.(=)
+/. 7 c.1060A>G r.(?) p.(Thr354Ala)
-/. - c.1066G>A r.(?) p.(Gly356Ser)
-?/. - c.1066G>A r.(?) p.(Gly356Ser)
-/. - c.1066G>A r.(?) p.(Gly356Ser)
?/. - c.1066G>A r.(?) p.(Gly356Ser)
-?/. - c.1066G>A r.(?) p.(Gly356Ser)
-?/. - c.1116G>A r.(?) p.(Thr372=)
?/. - c.1171C>G r.(?) p.(His391Asp)
+/. 7 c.1177G>A r.(?) p.(Gly393Ser)
?/. - c.1180C>T r.(?) p.(Pro394Ser)
-?/. - c.1214+4C>T r.spl? p.?
+?/. - c.1256_1259dup r.(?) p.(Ser421ValfsTer40)
?/. - c.1339C>T r.(?) p.(Arg447Trp)
-?/. - c.1347G>A r.(?) p.(Leu449=)
-?/. - c.1358C>T r.(?) p.(Ala453Val)
-?/. - c.1373-6_1373-5del r.spl? p.?
-?/. - c.1373-3C>T r.spl? p.?
+/. 9 c.1397A>C r.(?) p.(Gln466Pro)
+/. - c.1418_1419del r.(?) p.(Thr473Serfs*9)
+/. 9 c.1480C>T r.(?) p.(Gln494*)
?/. - c.1481A>G r.(?) p.(Gln494Arg)
?/. - c.1499C>T r.(?) p.(Ala500Val)
-?/. - c.1499C>T r.(?) p.(Ala500Val)
-?/. - c.1499C>T r.(?) p.(Ala500Val)
-?/. - c.1499C>T r.(?) p.(Ala500Val)
?/. - c.1504G>A r.(?) p.(Asp502Asn)
+/. 9 c.1567_1582del r.(?) p.(Glu523Thrfs*?)
?/. - c.1598A>C r.(?) p.(Glu533Ala)
-?/. - c.*452C>G r.(=) p.(=)
-?/. - c.*452C>T r.(=) p.(=)
-?/. - c.*452C>T r.(=) p.(=)
?/. - c.*454C>T r.(=) p.(=)
?/. - c.*454C>T r.(=) p.(=)
-/. - c.*455G>A r.(=) p.(=)
?/. - c.*473C>A r.(=) p.(=)
?/. - c.*485G>C r.(=) p.(=)
?/. - c.*533G>C r.(=) p.(=)
?/. - c.*533G>T r.(=) p.(=)
-?/. - c.*945G>A r.(=) p.(=)
-?/. - c.*945G>A r.(=) p.(=)
?/. - c.*1032G>A r.(=) p.(=)
-?/. - c.*1051T>C r.(=) p.(=)
?/. - c.*1065G>C r.(=) p.(=)
?/. - c.*1132_*1134del r.(=) p.(=)
+/. - c.*1133del r.(?) p.(=)
-?/. - c.*1268C>G r.(=) p.(=)
-?/. - c.*1317G>C r.(=) p.(=)
-/. - c.*1321A>G r.(=) p.(=)
+/. - c.*1434G>C r.(=) p.(=)
+?/. - c.*1458G>A r.(=) p.(=)
-?/. - c.*1570G>A r.(=) p.(=)
?/. - c.*1586C>G r.(=) p.(=)
-?/. - c.*1623G>T r.(=) p.(=)
-/. - c.*3430G>A r.(=) p.(=)
-?/. - c.*4605C>T r.(=) p.(=)
-?/. - c.*6310C>T r.(=) p.(=)
?/. - c.*6310C>T r.(=) p.(=)
+/. - c.*6325G>A r.(=) p.(=)
-/. - c.*6962_*6963insTT r.(=) p.(=)
-?/. - c.*7045C>T r.(=) p.(=)
-?/. - c.*7046G>C r.(=) p.(=)
-/. - c.*7084G>T r.(=) p.(=)
-?/. - c.*7135G>A r.(=) p.(=)
-?/. - c.*7135G>A r.(=) p.(=)
-?/. - c.*7135G>A r.(=) p.(=)
-?/. - c.*7136C>T r.(=) p.(=)
-/. - c.*7145T>C r.(=) p.(=)
?/. - c.*7154C>T r.(=) p.(=)
?/. - c.*7218C>T r.(=) p.(=)
?/. - c.*7361C>T r.(=) p.(=)
-?/. - c.*7775G>A r.(=) p.(=)
?/. - c.*7802_*7804del r.(=) p.(=)
-?/. - c.*7934G>A r.(=) p.(=)
-/. - c.*7934G>A r.(=) p.(=)
+/. - c.*7941del r.(?) p.(=)
?/. - c.*7942G>C r.(=) p.(=)
-?/. - c.*7942G>C r.(=) p.(=)
+?/. - c.*9299G>C r.(=) p.(=)
-/. - c.*9324C>T r.(=) p.(=)
-?/. - c.*9369G>A r.(=) p.(=)
-/. - c.*12432C>A r.(=) p.(=)
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