Transcript #00001437 (NM_001083961.1, WDR62 gene)

Transcript name transcript variant 1
Gene name WDR62 (WD repeat domain 62)
Chromosome 19
Transcript - NCBI ID NM_001083961.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001077430.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-09-13 13:33:24 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.102G>C r.(?) p.(Pro34=)
+?/. - c.141dup r.(?) p.(Leu48ThrfsTer32)
-?/. - c.142C>T r.(?) p.(Leu48Phe)
-?/. - c.142C>T r.(?) p.(Leu48Phe)
-/. - c.142C>T r.(?) p.(Leu48Phe)
+/. - c.177+1G>T r.spl p.?
-/. - c.180G>A r.(?) p.(Val60=)
-/. - c.180G>A r.(?) p.(Val60=)
-/. - c.186C>T r.(?) p.(Leu62=)
-/. - c.186C>T r.(?) p.(Leu62=)
+/. - c.250dup r.(250dup) p.(His84Profs*25)
-?/. - c.253G>A r.(?) p.(Val85Met)
?/. - c.253G>A r.(?) p.(Val85Met)
-?/. - c.269+12del r.(=) p.(=)
+/. 3 c.332G>C r.[270_332del,332_333ins332+1_332+87] p.[Cys91_Arg111del,Arg111ThrfsTer2]
+/. 3 c.332G>C r.[(270_332del,332_333ins332+1_332+87)] p.[(Cys91_Arg111del,Arg111ThrfsTer2)]
?/. - c.497A>G r.(?) p.(Asn166Ser)
?/. - c.511G>A r.(?) p.(Val171Met)
-/. - c.562-13C>T r.(=) p.(=)
-/. - c.562-13C>T r.(=) p.(=)
-?/. - c.570C>T r.(?) p.(Ile190=)
?/. - c.589G>A r.(?) p.(Val197Ile)
-?/. 6 c.589G>A r.(?) p.(Val197Ile)
-?/. - c.656G>A r.(?) p.(Arg219His)
-?/. - c.660T>C r.(?) p.(His220=)
-/. - c.700-18C>T r.(=) p.(=)
-/. - c.700-18C>T r.(=) p.(=)
-/. - c.700-18C>T r.(=) p.(=)
?/. - c.744C>T r.(?) p.(Gly248=)
-?/. - c.764_766del r.(?) p.(Phe255del)
-/. - c.866A>G r.(?) p.(Lys289Arg)
+/. 7i_9i c.883-1272_1234-850del r.(883_1233del) p.?
?/. - c.938C>A r.(?) p.(Thr313Lys)
?/. - c.1043+3A>G r.spl? p.?
+/. - c.1043+3A>G r.spl p.?
+/. - c.1043+3A>G r.spl p.?
?/. - c.1169A>G r.(?) p.(Asp390Gly)
+/. 9 c.1194G>A r.(?) p.(Trp398Ter)
-?/. - c.1218C>T r.(?) p.(Tyr406=)
-/. - c.1233+13C>T r.(=) p.(=)
-/. - c.1233+13C>T r.(=) p.(=)
+?/. 10 c.1313G>A r.(?) p.(Arg438His)
-?/. - c.1370A>G r.(?) p.(Asn457Ser)
-/. - c.1371+12C>T r.(=) p.(=)
-?/. - c.1425G>A r.(?) p.(Met475Ile)
-/. - c.1470C>T r.(?) p.(Asp490=)
-/. - c.1470C>T r.(?) p.(Asp490=)
+/. - c.1521G>A r.spl p.?
+?/. - c.1526C>T r.(?) p.(Ser509Leu)
+?/. - c.1531G>A r.(?) p.(Asp511Asn)
+/. - c.1531G>A r.(?) p.(Asp511Asn)
?/. - c.1576G>A r.(?) p.(Glu526Lys)
+?/. - c.1598A>G r.(?) p.(His533Arg)
?/. 12 c.1598A>G r.(?) p.(His533Arg)
-/. - c.1641G>A r.(?) p.(Thr547=)
-/. - c.1641G>A r.(?) p.(Thr547=)
-?/. - c.1642+8C>T r.(=) p.(=)
-?/. - c.1642+8C>T r.(=) p.(=)
-/. - c.1643-10C>T r.(=) p.(=)
-/. - c.1643-10C>T r.(=) p.(=)
?/. - c.1724C>T r.(?) p.(Thr575Met)
?/. - c.1742C>T r.(?) p.(Ser581Phe)
-/. - c.1768+18C>T r.(=) p.(=)
-?/. - c.1769-7C>T r.(=) p.(=)
+/. - c.1822del r.(?) p.(Arg608AlafsTer18)
?/. - c.1836+2T>G r.spl? p.?
?/. - c.1873G>A r.(?) p.(Val625Ile)
?/. - c.1903G>C r.(?) p.(Asp635His)
+?/. 15i c.1959-2A>G r.spl p.?
-?/. - c.1987A>C r.(?) p.(Lys663Gln)
?/. - c.2035-125C>T r.(=) p.(=)
?/. - c.2035-115T>A r.(=) p.(=)
?/. - c.2035-115T>C r.(=) p.(=)
?/. - c.2112G>A r.(?) p.(=)
+?/. - c.2146+1G>A r.spl? p.?
?/. 18 c.2210G>C r.(?) p.(Ser737Thr)
-?/. - c.2211-4G>A r.spl? p.?
-/. - c.2271G>A r.(?) p.(Leu757=)
-/. - c.2271G>A r.(?) p.(Leu757=)
-/. - c.2281C>T r.(?) p.(His761Tyr)
-/. - c.2312A>G r.(?) p.(Lys771Arg)
-/. - c.2334-29C>T r.(=) p.(=)
-/. - c.2334-6C>A r.(=) p.(=)
?/. - c.2343G>A r.(?) p.(Thr781=)
?/. - c.2418T>G r.(?) p.(Cys806Trp)
-/. - c.2467+46_2467+47del r.(=) p.(=)
+/. - c.2508G>A r.(?) p.(Trp836Ter)
+/. - c.2508G>A r.(?) p.(Trp836Ter)
+/. - c.2508G>A r.(?) p.(Trp836Ter)
+?/. - c.2520+1G>T r.spl p.(Leu840Leufs*95)
+/. 21i c.2520+5G>T r.(2468_2520del) p.?
+/. - c.2520+5G>T r.spl p.?
+/. - c.2520+5G>T r.spl p.?
+/. - c.2520+5G>T r.spl p.?
+/. - c.2520+5G>T r.spl p.?
-/. - c.2549T>C r.(?) p.(Leu850Ser)
-/. - c.2549T>C r.(?) p.(Leu850Ser)
-/. - c.2549T>C r.(?) p.(Leu850Ser)
-?/. - c.2560G>A r.(?) p.(Ala854Thr)
-?/. - c.2605G>A r.(?) p.(Gly869Ser)
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