Transcript #00000436 (NM_020922.4, WNK3 gene)

Transcript name transcript variant 1
Gene name WNK3 (WNK lysine deficient protein kinase 3)
Chromosome X
Transcript - NCBI ID NM_020922.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_065973.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2012-09-13 12:14:51 +02:00 (CEST)
Date last edited N/A


Variants

63 entries on 1 page. Showing entries 1 - 63.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-120+3053G>A r.(=) p.(=)
-?/. - c.-119-6del r.(=) p.(=)
?/. - c.29G>A r.(?) p.(Ser10Asn)
-?/. - c.146C>G r.(?) p.(Ser49Cys)
?/. - c.223T>G r.(?) p.(Ser75Ala)
-?/. - c.223T>G r.(?) p.(Ser75Ala)
?/. - c.250G>A r.(?) p.(Ala84Thr)
?/. - c.904C>T r.(?) p.(Arg302Cys)
?/. - c.985G>A r.(?) p.(Val329Ile)
?/. - c.985G>A r.(?) p.(Val329Ile)
?/. - c.985G>A r.(?) p.(Val329Ile)
+?/. - c.1089+1G>A r.spl p.?
-?/. 7 c.1206T>C r.(?) p.(=)
?/. - c.1399-54dup r.(=) p.(=)
?/. 8 c.1667C>G r.(?) p.(Pro556Arg)
-?/. - c.1694-4A>G r.spl? p.?
-?/. - c.1917G>A r.(?) p.(Pro639=)
?/. - c.2018A>G r.(?) p.(Gln673Arg)
?/. - c.2037+180_2037+181dup r.(=) p.(=)
?/. - c.2037+181dup r.(=) p.(=)
?/. - c.2123C>T r.(?) p.(Thr708Ile)
-?/. - c.2126C>T r.(?) p.(Thr709Met)
-?/. 12 c.2169C>A r.(?) p.(=)
-?/. - c.2359G>C r.(?) p.(Asp787His)
?/. - c.2367+4dup r.spl? p.?
-?/. - c.2413G>C r.(?) p.(Glu805Gln)
?/. - c.2417A>T r.(?) p.(Glu806Val)
?/. - c.2440G>A r.(?) p.(Ala814Thr)
?/. - c.2489T>G r.(?) p.(Val830Gly)
?/. - c.2746C>T r.(?) p.(Arg916Trp)
-?/. - c.2969A>C r.(?) p.(Glu990Ala)
-?/. - c.3218C>T r.(?) p.(Thr1073Ile)
?/. - c.3395C>T r.(?) p.(Pro1132Leu)
?/. - c.3652-105dup r.(=) p.(=)
?/. - c.3652-105dup r.(=) p.(=)
?/. - c.3652-105dup r.(=) p.(=)
?/. - c.3652-105dup r.(=) p.(=)
?/. - c.3652-29_3652-10del r.(=) p.(=)
./. - c.3652_*195729del r.? p.?
?/. - c.3776G>C r.(?) p.(Ser1259Thr)
?/. 18 c.3841C>T r.(?) p.(Arg1281Trp)
-/. - c.3884T>C r.(?) p.(Val1295Ala)
?/. - c.4000C>T r.(?) p.(Arg1334Trp)
-?/. - c.4015-4T>C r.spl? p.?
-?/. - c.4021A>T r.(?) p.(Thr1341Ser)
-?/. - c.4121A>G r.(?) p.(Lys1374Arg)
?/. 20 c.4219A>G r.(?) p.(Lys1407Glu)
?/. - c.4564A>G r.(?) p.(Ser1522Gly)
?/. - c.4629-241del r.(=) p.(=)
?/. - c.4629-241del r.(=) p.(=)
?/. - c.4795C>T r.(?) p.(Arg1599Cys)
-?/. - c.4795C>T r.(?) p.(Arg1599Cys)
?/. - c.4928A>C r.(?) p.(Lys1643Thr)
?/. - c.4929dup r.(?) p.(Gly1644Argfs*6)
?/. - c.5123C>G r.(?) p.(Ser1708Cys)
-?/. - c.5243C>T r.(?) p.(Ala1748Val)
-?/. - c.5362T>C r.(?) p.(Ser1788Pro)
-?/. - c.5372A>T r.(?) p.(Asn1791Ile)
?/. - c.*371_*372del r.(=) p.(=)
?/. - c.*1866del r.(=) p.(=)
?/. - c.*1918del r.(=) p.(=)
?/. - c.*1918del r.(=) p.(=)
?/. - c.*5311del r.(=) p.(=)
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