Transcript #00024655 (NM_014727.1, KMT2B gene)

Transcript name lysine (K)-specific methyltransferase 2B
Gene name KMT2B (lysine methyltransferase 2B)
Chromosome 19
Transcript - NCBI ID NM_014727.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_055542.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2017-08-08 13:22:00 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.-16_*320{0} r.0 p.0
+/. - c.-16_*320{0} r.0 p.0
+/. - c.-16_*320{0} r.0 p.0
+/. - c.-16_*320{0} r.0 p.0
+/. - c.-16_*320{0} r.0 p.0
+/. - c.-16_*320{0} r.0 p.0
+/. - c.-16_*320{0} r.0 p.0
+/. - c.-16_*320{0} r.0 p.0
+/. - c.-16_*320{0} r.0 p.0
+/. - c.-16_*320{0} r.0 p.0
+/. - c.-16_*320{0} r.0 p.0
+/. - c.-16_*320{0} r.0 p.0
+/. - c.-16_*320{0} r.0 p.0
+/. - c.-16_*320{0} r.0 p.0
+/. - c.-16_*320{0} r.0 p.0
+/. - c.-16_*320{0} r.0 p.0
+/. - c.-16_*320{0} r.0 p.0
+/. - c.-16_*320{0} r.0 p.0
-?/. - c.130C>T r.(?) p.(Arg44Trp)
-?/. - c.180G>C r.(?) p.(Glu60Asp)
-?/. - c.221G>A r.(?) p.(Arg74His)
?/. - c.221G>A r.(?) p.(Arg74His)
-?/. - c.306C>A r.(?) p.(Gly102=)
-?/. - c.398C>T r.(?) p.(Ala133Val)
-?/. - c.516C>A r.(?) p.(Thr172=)
?/. - c.535C>T r.(?) p.(Arg179Trp)
?/. - c.586C>T r.(?) p.(Leu196Phe)
-?/. - c.625C>T r.(?) p.(Arg209Trp)
-?/. - c.626G>A r.(?) p.(Arg209Gln)
?/. - c.640T>C r.(?) p.(Ser214Pro)
-?/. - c.649C>T r.(?) p.(Arg217Trp)
+?/. 3 c.649del r.(649del) p.(Arg217Glyfs*22)
+?/. - c.651_654del r.(?) p.(Arg218Leufs*20)
?/. - c.745A>G r.(?) p.(Lys249Glu)
-?/. - c.759A>G r.(?) p.(Pro253=)
?/. - c.883C>T r.(?) p.(Arg295Cys)
-?/. - c.885C>T r.(?) p.(Arg295=)
+/. - c.889C>T r.(?) p.(Arg297Ter)
?/. - c.971A>G r.(?) p.(Glu324Gly)
?/. - c.988_993del r.(?) p.(Gly330_Gln331del)
-?/. - c.1028G>A r.(?) p.(Arg343Lys)
-?/. - c.1090G>A r.(?) p.(Glu364Lys)
-?/. - c.1090G>A r.(?) p.(Glu364Lys)
-?/. - c.1097A>G r.(?) p.(Glu366Gly)
-?/. - c.1117_1119del r.(?) p.(Glu373del)
-?/. - c.1126_1128del r.(?) p.(Lys376del)
?/. - c.1144G>A r.(?) p.(Glu382Lys)
?/. - c.1160C>T r.(?) p.(Ala387Val)
-?/. - c.1169T>C r.(?) p.(Met390Thr)
?/. - c.1209_1211del r.(?) p.(Pro405del)
-?/. - c.1212G>A r.(?) p.(Pro404=)
?/. - c.1272_1274del r.(?) p.(Pro427del)
-?/. - c.1398C>T r.(?) p.(Ser466=)
-/. - c.1471G>A r.(?) p.(Gly491Ser)
-?/. - c.1504G>A r.(?) p.(Ala502Thr)
?/. - c.1566G>C r.(?) p.(Lys522Asn)
?/. - c.1573C>T r.(?) p.(Arg525Trp)
-?/. - c.1756G>A r.(?) p.(Ala586Thr)
?/. - c.1790C>T r.(?) p.(Pro597Leu)
+?/. - c.1808dup r.(?) p.(Leu604Profs*72)
+/. - c.1810dup r.(?) p.(Leu604Profs*72)
-?/. - c.1858C>A r.(?) p.(Pro620Thr)
?/. - c.1858C>G r.(?) p.(Pro620Ala)
-?/. - c.1909C>T r.(?) p.(Pro637Ser)
-?/. - c.1952A>G r.(?) p.(Gln651Arg)
?/. - c.2050G>A r.(?) p.(Ala684Thr)
-?/. - c.2053G>A r.(?) p.(Asp685Asn)
+?/. 3 c.2061_2062del r.(?) p.(Pro688Serfs*2)
-?/. - c.2078C>T r.(?) p.(Pro693Leu)
?/. - c.2084C>T r.(?) p.(Ala695Val)
-?/. - c.2183G>A r.(?) p.(Ser728Asn)
-?/. - c.2265A>G r.(?) p.(Pro755=)
-?/. - c.2268_2279dup r.(?) p.(Gln759_Pro762dup)
-?/. - c.2268_2279dup r.(?) p.(Gln759_Pro762dup)
?/. - c.2332G>T r.(?) p.(Ala778Ser)
-?/. - c.2338G>C r.(?) p.(Val780Leu)
-?/. - c.2385C>T r.(?) p.(Leu795=)
-?/. - c.2439G>C r.(?) p.(Lys813Asn)
?/. - c.2447C>T r.(?) p.(Ala816Val)
-?/. - c.2462G>T r.(?) p.(Ser821Ile)
-?/. - c.2475G>T r.(?) p.(Gln825His)
-?/. - c.2489C>A r.(?) p.(Ala830Asp)
?/. - c.2491G>A r.(?) p.(Gly831Arg)
-?/. - c.2519G>A r.(?) p.(Gly840Asp)
-?/. - c.2565G>A r.(?) p.(Arg855=)
?/. - c.2681G>T r.(?) p.(Ser894Ile)
-?/. - c.2716A>C r.(?) p.(Thr906Pro)
?/. - c.2716A>C r.(?) p.(Thr906Pro)
-?/. - c.2723-5A>G r.spl? p.?
-?/. - c.2735C>T r.(?) p.(Ala912Val)
-?/. - c.2756C>T r.(?) p.(Pro919Leu)
?/. - c.2756C>T r.(?) p.(Pro919Leu)
?/. - c.2887A>G r.(?) p.(Met963Val)
?/. - c.2942G>A r.(?) p.(Cys981Tyr)
-/. - c.3059-3G>A r.spl? p.?
?/. - c.3065C>T r.(?) p.(Thr1022Met)
?/. - c.3077C>T r.(?) p.(Thr1026Met)
-?/. - c.3101A>C r.(?) p.(Glu1034Ala)
?/. - c.3163C>T r.(?) p.(Arg1055Trp)
?/. - c.3206C>G r.(?) p.(Ser1069Cys)
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