Transcript #00002992 (NM_004318.3, ASPH gene)

Transcript name transcript variant 1
Gene name ASPH (aspartate beta-hydroxylase)
Chromosome 8
Transcript - NCBI ID NM_004318.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_004309.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

89 entries on 1 page. Showing entries 1 - 89.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.34_51dup r.(?) p.(Asn12_Gly17dup)
-?/. - c.61G>A r.(?) p.(Gly21Ser)
-/. - c.69G>T r.(?) p.(Thr23=)
-?/. - c.69G>T r.(?) p.(Thr23=)
-?/. - c.76G>C r.(?) p.(Gly26Arg)
-?/. - c.103+7G>A r.(=) p.(=)
-?/. - c.147C>T r.(?) p.(Leu49=)
-/. - c.216C>T r.(?) p.(Val72=)
?/. - c.239A>G r.(?) p.(Tyr80Cys)
?/. - c.248T>C r.(?) p.(Val83Ala)
?/. - c.254-1429G>A r.(=) p.(=)
-?/. - c.254-1396T>A r.(=) p.(=)
?/. - c.257A>G r.(?) p.(Lys86Arg)
?/. - c.311A>G r.(?) p.(Lys104Arg)
-/. - c.322+4801_322+4803dup r.(=) p.(=)
-?/. - c.322+4870A>C r.(=) p.(=)
-?/. - c.322+12706_322+12707insTCCCA r.(=) p.(=)
-?/. - c.322+12706_322+12707insTCCCA r.(=) p.(=)
-?/. - c.322+12708T>A r.(=) p.(=)
-?/. - c.322+12708T>A r.(=) p.(=)
-?/. - c.322+12708T>A r.(=) p.(=)
-?/. - c.322+12710_322+12711insGAC r.(=) p.(=)
-?/. - c.322+12710_322+12711insGAC r.(=) p.(=)
-?/. - c.322+12725A>G r.(=) p.(=)
-?/. - c.322+12728G>A r.(=) p.(=)
-?/. - c.322+12733A>G r.(=) p.(=)
-?/. - c.323-11828A>G r.(=) p.(=)
-?/. - c.323-11810A>G r.(=) p.(=)
?/. - c.323-11633T>G r.(=) p.(=)
-?/. - c.323-11619A>G r.(=) p.(=)
?/. - c.323-11619A>G r.(=) p.(=)
-?/. - c.323-11612T>C r.(=) p.(=)
-/. - c.323-11612T>C r.(=) p.(=)
?/. - c.358C>T r.(?) p.(Pro120Ser)
-?/. - c.363A>G r.(?) p.(Pro121=)
-?/. - c.441A>C r.(?) p.(Ala147=)
?/. - c.481G>A r.(?) p.(Ala161Thr)
-?/. - c.518del r.(?) p.(Asp173Valfs*20)
-?/. - c.567G>A r.(?) p.(Ala189=)
-?/. - c.575T>C r.(?) p.(Val192Ala)
-?/. - c.620-5del r.spl? p.?
-/. - c.620-5del r.spl? p.?
-/. - c.647A>G r.(?) p.(Glu216Gly)
-/. - c.758-4del r.spl? p.?
-/. - c.758-4dup r.spl? p.?
-?/. - c.758-4dup r.spl? p.?
-/. - c.791-14T>G r.(=) p.(=)
-/. - c.791-4_791-3dup r.spl? p.?
?/. - c.791-4_791-3dup r.spl? p.?
-/. - c.791-3del r.spl? p.?
-/. - c.791-3dup r.spl? p.?
-?/. - c.791-3dup r.spl? p.?
-?/. - c.791-3T>C r.spl? p.?
-/. - c.844C>T r.(?) p.(Pro282Ser)
-/. - c.844C>T r.(?) p.(Pro282Ser)
-?/. - c.844C>T r.(?) p.(Pro282Ser)
-?/. - c.844C>T r.(?) p.(Pro282Ser)
+?/. - c.886G>T r.(?) p.(Glu296*)
-?/. - c.1026A>G r.(?) p.(Lys342=)
-?/. - c.1026A>G r.(?) p.(Lys342=)
-?/. - c.1062+4G>A r.spl? p.?
+?/. - c.1126C>T r.(?) p.(Arg376Ter)
+?/. - c.1126C>T r.(?) p.(Arg376Ter)
+/. - c.1126C>T r.(?) p.(Arg376*)
+/. - c.1126C>T r.(?) p.(Arg376*)
-/. - c.1146G>A r.(?) p.(Ala382=)
?/. - c.1176_1178del r.(?) p.(Arg393del)
?/. - c.1207G>A r.(?) p.(Glu403Lys)
?/. - c.1274G>A r.(?) p.(Arg425His)
?/. - c.1298T>G r.(?) p.(Leu433Arg)
+/. - c.1375del r.(?) p.(Asp459Thrfs*8)
+?/. - c.1566_1567del r.(?) p.(Asp523*)
-/. - c.1626+10A>G r.(=) p.(=)
-/. - c.1627-20del r.(=) p.(=)
+?/. - c.1627-1G>A r.spl? p.?
+?/. - c.1627-1G>A r.spl? p.?
-?/. - c.1665C>T r.(?) p.(His555=)
?/. - c.1768T>G r.(?) p.(Leu590Val)
?/. - c.1862A>G r.(?) p.(Glu621Gly)
-/. - c.1900+6T>C r.(=) p.(=)
?/. - c.1976G>C r.(?) p.(Gly659Ala)
+?/. - c.2075G>A r.(?) p.(Gly692Asp)
+/. - c.2118del r.(?) p.(Asn706Lysfs*31)
+?/. - c.2118del r.(?) p.(Asn706Lysfs*31)
-/. - c.2127-6C>T r.(=) p.(=)
?/. - c.2140G>C r.(?) p.(Gly714Arg)
+/. - c.2181_2183dup r.(?) p.(Trp728*)
?/. - c.2203C>T r.(?) p.(Arg735Trp)
+/. - c.2204G>A r.(?) p.(Arg735Gln)
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