Transcript #00006951 (NM_024757.4, EHMT1 gene)

Transcript name transcript variant 1
Gene name EHMT1 (euchromatic histone-lysine N-methyltransferase 1)
Chromosome 9
Transcript - NCBI ID NM_024757.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_079033.4
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-4736C>T r.(?) p.(=)
-?/. - c.-4242C>T r.(?) p.(=)
+/. _1_27_ c.-37_*1174{0} r.0 p.0
+/. _1_27_ c.-37_*1174{0} r.0 p.0
+/. _1_27_ c.-37_*1174{0} r.0 p.0
+/. _1_27_ c.-37_*1174{0} r.0 p.0
+/. _1_27_ c.-37_*1174{0} r.0 p.0
+/. _1_27_ c.-37_*1174{0} r.0 p.0
+/. _1_27_ c.-37_*1174{0} r.0 p.0
+/. _1_27_ c.-37_*1174{0} r.0 p.0
+/. _1_27_ c.-37_*1174{0} r.0 p.0
+/. _1_9 c.? r.0 p.0
-?/. - c.21+8503G>A r.(=) p.(=)
-?/. - c.22-40770T>G r.(=) p.(=)
-?/. - c.22-34459_22-34458insA r.(=) p.(=)
+/. - c.34_35insC r.(?) p.(Arg12Thrfs*25)
-?/. - c.35G>C r.(?) p.(Arg12Thr)
-?/. - c.40dup r.(?) p.(Glu14Glyfs*23)
-?/. - c.44C>T r.(?) p.(Pro15Leu)
-?/. - c.85+312G>A r.(=) p.(=)
-?/. - c.86-478_86-477dup r.(=) p.(=)
-?/. - c.86-304_86-303dup r.(=) p.(=)
-?/. - c.86-304_86-303insAG r.(=) p.(=)
-?/. - c.86-274dup r.(=) p.(=)
-?/. - c.86-236_86-234del r.(=) p.(=)
-?/. - c.86-228A>G r.(=) p.(=)
-?/. - c.86-220_86-219dup r.(=) p.(=)
-?/. - c.86-195_86-193del r.(=) p.(=)
-?/. - c.86-178_86-176del r.(=) p.(=)
-?/. - c.86-170A>G r.(=) p.(=)
-?/. - c.86-153T>G r.(=) p.(=)
-?/. - c.86-132dup r.(=) p.(=)
-/. - c.148G>A r.(?) p.(Ala50Thr)
-?/. - c.149C>G r.(?) p.(Ala50Gly)
-?/. - c.149C>T r.(?) p.(Ala50Val)
-?/. - c.159G>T r.(?) p.(Glu53Asp)
?/. - c.170C>G r.(?) p.(Ser57Cys)
-?/. - c.200C>G r.(?) p.(Ala67Gly)
?/. - c.224A>T r.(?) p.(Asp75Val)
-?/. - c.229G>A r.(?) p.(Ala77Thr)
+/. - c.244del r.(?) p.(Gln82ArgfsTer7)
-?/. - c.271A>T r.(?) p.(Ile91Leu)
+/. - c.294_297del r.(?) p.(Arg99Thrfs*28)
-?/. - c.337G>A r.(?) p.(Asp113Asn)
-?/. - c.354T>G r.(?) p.(Ser118=)
-?/. - c.388C>G r.(?) p.(Pro130Ala)
-?/. - c.390G>T r.(?) p.(Pro130=)
-?/. - c.405G>T r.(?) p.(Gln135His)
?/. - c.431C>A r.(?) p.(Ala144Asp)
-/. - c.432C>T r.(?) p.(Ala144=)
-?/. - c.432C>T r.(?) p.(Ala144=)
?/. - c.437C>T r.(?) p.(Ser146Leu)
+/. - c.439C>G r.(?) p.(Leu147Val)
-/. - c.444T>C r.(?) p.(Pro148=)
-?/. - c.466C>G r.(?) p.(Pro156Ala)
-?/. - c.480C>T r.(?) p.(Gly160=)
-/. - c.480C>T r.(?) p.(Gly160=)
-?/. - c.482A>G r.(?) p.(Lys161Arg)
?/. - c.497G>C r.(?) p.(Ser166Thr)
-/. - c.526C>T r.(?) p.(Pro176Ser)
?/. - c.529G>C r.(?) p.(Ala177Pro)
-?/. - c.576G>A r.(?) p.(Pro192=)
-?/. - c.576G>A r.(?) p.(Pro192=)
-?/. - c.578C>T r.(?) p.(Ala193Val)
-?/. - c.581C>T r.(?) p.(Pro194Leu)
?/. - c.623C>T r.(?) p.(Pro208Leu)
-?/. - c.624G>A r.(?) p.(Pro208=)
-?/. - c.631G>A r.(?) p.(Val211Ile)
-?/. - c.632T>C r.(?) p.(Val211Ala)
?/. - c.632T>C r.(?) p.(Val211Ala)
-?/. - c.642+4047del r.(=) p.(=)
-?/. - c.642+4109A>G r.(=) p.(=)
+?/. - c.643-2A>G r.(?) p.(?)
+/. - c.673C>T r.(?) p.(Arg225*)
?/. - c.704A>G r.(?) p.(Glu235Gly)
+/. - c.736C>T r.(?) p.(Arg246Ter)
-?/. - c.737G>A r.(?) p.(Arg246Gln)
?/. - c.750A>C r.(?) p.(Leu250Phe)
-?/. - c.770A>C r.(?) p.(His257Pro)
+/. - c.823G>A r.(?) p.(Ala275Thr)
+/. - c.823+1G>T r.spl p.?
-?/. - c.824-2A>T r.spl? p.?
-/. - c.824-2A>T r.spl? p.?
?/. - c.824-2_824del r.spl? p.?
-?/. - c.824-1G>T r.spl? p.?
-/. - c.824-1G>T r.spl? p.?
-/. - c.824C>T r.(?) p.(Ala275Val)
-?/. - c.827G>T r.(?) p.(Cys276Phe)
?/. - c.827_828del r.(?) p.(Cys276PhefsTer21)
-?/. - c.831G>T r.(?) p.(Leu277Phe)
-?/. - c.831_833del r.(?) p.(Leu277_Pro278delinsPhe)
-?/. - c.832C>T r.(?) p.(Pro278Ser)
-?/. - c.833C>T r.(?) p.(Pro278Leu)
-?/. - c.837_838insTTTTTTTT r.(?) p.(Val280PhefsTer5)
-?/. - c.838G>T r.(?) p.(Val280Phe)
+/. - c.861del r.(?) p.(Lys288Argfs*20)
+/. 5 c.871C>T r.(?) p.(Arg291*)
?/. 5 c.905A>G r.(?) p.(Lys302Arg)
-?/. - c.905A>G r.(?) p.(Lys302Arg)
-?/. - c.905A>G r.(?) p.(Lys302Arg)
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