Transcript #00001334 (NM_015015.2, KDM4B gene)

Transcript name lysine (K)-specific demethylase 4B
Gene name KDM4B (lysine (K)-specific demethylase 4B)
Chromosome 19
Transcript - NCBI ID NM_015015.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_055830.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-09-13 13:27:10 +02:00 (CEST)
Date last edited N/A


Variants

67 entries on 1 page. Showing entries 1 - 67.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-3725_-3724dup r.(?) p.(=)
-?/. - c.-25-305C>T r.(=) p.(=)
?/. - c.162G>A r.(?) p.(Trp54*)
-?/. - c.231G>A r.(?) p.(Thr77=)
+/. - c.288C>T r.287_317del p.Glu97Thrfs∗66
+/. - c.371_374del r.(?) p.(Lys124Thrfs*48)
+?/. - c.432+1G>A r.spl? p.?
?/. - c.432+1G>C r.spl? p.?
-?/. - c.433-9G>A r.(=) p.(=)
-?/. - c.433-4A>G r.spl? p.?
-?/. - c.433-4A>G r.spl? p.?
?/. - c.455G>C r.(?) p.(Gly152Ala)
?/. - c.659T>C r.(?) p.(Leu220Pro)
+/. - c.659T>C r.(?) p.(Leu220Pro)
-?/. - c.664C>A r.(?) p.(Arg222=)
+/. - c.664C>T r.(?) p.(Arg222Trp)
?/. - c.865T>C r.(?) p.(Ser289Pro)
-?/. - c.882C>A r.(?) p.(Thr294=)
-?/. - c.900C>T r.(?) p.(Tyr300=)
?/. - c.919-8508T>C r.(=) p.(=)
-?/. - c.919-5C>T r.spl? p.?
?/. - c.953T>C r.(?) p.(Met318Thr)
?/. - c.1084C>T r.(?) p.(Arg362Trp)
?/. - c.1099G>A r.(?) p.(Ala367Thr)
-?/. - c.1115+558del r.(=) p.(=)
-?/. - c.1115+721G>A r.(=) p.(=)
-?/. - c.1115+958C>G r.(=) p.(=)
-?/. - c.1115+1001C>G r.(=) p.(=)
?/. - c.1115+1112C>T r.(=) p.(=)
?/. - c.1148C>T r.(?) p.(Pro383Leu)
?/. - c.1183A>T r.(?) p.(Thr395Ser)
?/. - c.1270_1272dup r.(?) p.(Glu424dup)
?/. - c.1334_1337dup r.(?) p.(Pro447Alafs*62)
-?/. - c.1352A>C r.(?) p.(Lys451Thr)
-?/. - c.1401_1402insGGG r.(?) p.(Pro467_Pro468insGly)
-?/. - c.1453C>G r.(?) p.(Leu485Val)
-?/. - c.1454T>C r.(?) p.(Leu485Pro)
-?/. - c.1463C>T r.(?) p.(Pro488Leu)
-?/. - c.1525G>A r.(?) p.(Val509Met)
-?/. - c.1598C>T r.(?) p.(Pro533Leu)
-?/. - c.1640G>A r.(?) p.(Cys547Tyr)
?/. - c.1750C>T r.(?) p.(Arg584Cys)
+/. - c.1778_1779del r.(?) p.(Glu593Glyfs*41)
?/. - c.1838A>G r.(?) p.(His613Arg)
-?/. - c.1850G>A r.(?) p.(Arg617Gln)
-?/. - c.1906+7G>C r.(=) p.(=)
+/. - c.1907-1G>C r.spl p.?
-?/. - c.2092C>A r.(?) p.(Gln698Lys)
+/. - c.2221dup r.(?) p.(Glu741Glyfs*41)
?/. - c.2278T>A r.(?) p.(Cys760Ser)
+/. - c.2303A>G r.(?) p.(His768Arg)
?/. - c.2360G>C r.(?) p.(Arg787Pro)
?/. - c.2555_2560del r.(?) p.(Cys852_Val853del)
?/. - c.2566C>T r.(?) p.(Arg856Trp)
?/. - c.2716C>T r.(?) p.(His906Tyr)
-?/. - c.2734G>A r.(?) p.(Ala912Thr)
-?/. - c.2793C>T r.(?) p.(Asn931=)
?/. - c.2831C>T r.(?) p.(Ser944Leu)
-?/. - c.2875G>A r.(?) p.(Asp959Asn)
-?/. - c.3000C>T r.(?) p.(Ser1000=)
-?/. - c.3001G>A r.(?) p.(Val1001Ile)
?/. - c.3101T>C r.(?) p.(Val1034Ala)
?/. - c.3103C>T r.(?) p.(Arg1035Cys)
?/. - c.3125C>T r.(?) p.(Thr1042Met)
-?/. - c.3164C>T r.(?) p.(Ala1055Val)
-?/. - c.3172G>A r.(?) p.(Ala1058Thr)
+/. - c.3284C>T r.(?) p.(Pro1095Leu)
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