Transcript #00024080 (NM_199292.2, TH gene)

Transcript name transcript variant 1
Gene name TH (tyrosine hydroxylase)
Chromosome 11
Transcript - NCBI ID NM_199292.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_954986.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2015-12-01 08:07:55 +01:00 (CET)
Date last edited N/A


Variants

182 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.-71C>T r.(?) p.(=)
+/. _1 c.-71C>T r.? p.?
+/. _1 c.-70G>A r.? p.?
+/. _1 c.-70G>A r.? p.?
+/. _1 c.-70G>A r.? p.?
+/. _1 c.-69T>A r.? p.?
?/. - c.5C>T r.(?) p.(Pro2Leu)
-?/. - c.12C>T r.(?) p.(Pro4=)
-?/. - c.16G>A r.(?) p.(Ala6Thr)
-/. - c.16G>A r.(?) p.(Ala6Thr)
?/. - c.43C>T r.(?) p.(Arg15Cys)
-?/. - c.67G>A r.(?) p.(Ala23Thr)
?/. - c.67G>A r.(?) p.(Ala23Thr)
?/. - c.81G>T r.(?) p.(Glu27Asp)
+?/. - c.102+1G>A r.spl? p.?
-?/. - c.106G>A r.(?) p.(Ala36Thr)
?/. - c.124A>C r.(?) p.(Thr42Pro)
-?/. - c.134C>T r.(?) p.(Pro45Leu)
-?/. - c.197T>C r.(?) p.(Ile66Thr)
-?/. - c.197T>C r.(?) p.(Ile66Thr)
?/. - c.202C>T r.(?) p.(Arg68Cys)
+/. - c.295del r.(?) p.(Leu99TrpfsTer15)
+/. 3 c.295del r.(?) p.(Leu99Trpfs*15)
?/. - c.316G>A r.(?) p.(Glu106Lys)
-?/. - c.324G>C r.(?) p.(Glu108Asp)
-/. - c.334G>A r.(?) p.(Val112Met)
-/. - c.334G>A r.(?) p.(Val112Met)
-/. - c.334G>A r.(?) p.(Val112Met)
-/. - c.334G>A r.(?) p.(Val112Met)
-?/. - c.357G>A r.(?) p.(Pro119=)
-?/. - c.360G>A r.(?) p.(Arg120=)
-?/. - c.360G>A r.(?) p.(Arg120=)
-?/. - c.360G>A r.(?) p.(Arg120=)
?/. - c.386G>A r.(?) p.(Arg129Gln)
-?/. - c.397G>T r.(?) p.(Val133Leu)
-?/. - c.406-9C>T r.(=) p.(=)
?/. 3i c.406-3A>G r.spl p.?
-?/. - c.458G>A r.(?) p.(Arg153Gln)
?/. - c.484T>G r.(?) p.(Phe162Val)
?/. - c.484T>G r.(?) p.(Phe162Val)
?/. - c.487G>A r.(?) p.(Val163Met)
?/. - c.487G>A r.(?) p.(Val163Met)
?/. - c.487G>T r.(?) p.(Val163Leu)
?/. - c.499G>A r.(?) p.(Val167Met)
?/. - c.499G>A r.(?) p.(Val167Met)
-?/. - c.580+3G>A r.spl? p.?
-?/. - c.581-4A>G r.spl? p.?
?/. - c.625C>T r.(?) p.(His209Tyr)
-?/. - c.669G>A r.(?) p.(Pro223=)
-?/. - c.669+6_669+14del r.(=) p.(=)
-?/. - c.669+13C>T r.(=) p.(=)
-?/. - c.670-22C>G r.(=) p.(=)
-/. - c.670-22C>T r.(=) p.(=)
?/. - c.675C>A r.(?) p.(Phe225Leu)
?/. - c.677C>T r.(?) p.(Ser226Leu)
-?/. - c.687G>T r.(?) p.(Val229=)
+/. - c.698G>A r.(?) p.(Arg233His)
+/. - c.698G>A r.(?) p.(Arg233His)
+/. - c.698G>A r.(?) p.(Arg233His)
+/. - c.698G>A r.(?) p.(Arg233His)
+/. - c.698G>A r.(?) p.(Arg233His)
+/. - c.698G>A r.(?) p.(Arg233His)
+/. - c.698G>A r.(?) p.(Arg233His)
+/. - c.698G>A r.(?) p.(Arg233His)
+/. - c.698G>A r.(?) p.(Arg233His)
+/. - c.698G>A r.(698g>a) p.(Arg233His)
?/. - c.698G>A r.(?) p.(Arg233His)
+/. - c.698G>A r.(?) p.(Arg233His)
+?/. - c.698G>A r.(?) p.(Arg233His)
+/. - c.707T>C r.(?) p.(Leu236Pro)
+/. - c.707T>C r.(?) p.(Leu236Pro)
?/. - c.709A>C r.(?) p.(Ile237Leu)
+?/. - c.728A>C r.(?) p.(Gln243Pro)
-?/. - c.737+15C>A r.(=) p.(=)
-?/. - c.738C>T r.(?) p.(His246=)
?/. - c.739G>A r.(?) p.(Gly247Ser)
?/. 7 c.772G>A r.(?) p.(Glu258Lys)
-?/. - c.777G>A r.(?) p.(Glu259=)
-?/. - c.777G>A r.(?) p.(Glu259=)
-?/. - c.789-3C>T r.spl? p.?
-/. - c.813G>A r.(?) p.(Lys271=)
-/. - c.813G>A r.(?) p.(Lys271=)
-/. - c.813G>A r.(?) p.(Lys271=)
+/. - c.822C>A r.(?) p.(Tyr274*)
+/. - c.826A>C r.(?) p.(Thr276Pro)
+?/. - c.880G>C r.(?) p.(Gly294Arg)
?/. 8 c.919T>G r.(?) p.(Ser307Ala)
+/. - c.941C>T r.(?) p.(Thr314Met)
+/. - c.1010G>A r.(?) p.(Arg337His)
?/. - c.1016T>G r.(?) p.(Phe339Cys)
-/. - c.1070+8C>G r.(=) p.(=)
-/. - c.1070+8C>G r.(=) p.(=)
-/. - c.1070+8C>G r.(=) p.(=)
+/. - c.1076G>T r.(?) p.(Cys359Phe)
+/. - c.1108C>A r.(?) p.(Leu370Met)
?/. - c.1132T>G r.(?) p.(Phe378Val)
+?/. - c.1145T>C r.(?) p.(Ile382Thr)
+?/. - c.1154C>T r.(?) p.(Ala385Val)
?/. - c.1154C>T r.(?) p.(Ala385Val)
+?/. - c.1159C>A r.(?) p.(Leu387Met)
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