Transcript #00025711 (NM_000360.3, TH gene)

Transcript name transcript variant 2
Gene name TH (tyrosine hydroxylase)
Chromosome 11
Transcript - NCBI ID NM_000360.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000351.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2022-06-20 08:24:27 +02:00 (CEST)
Date last edited N/A


Variants

170 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.(=)
?/. - 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.44G>A r.(?) p.(Arg15His)
-?/. - c.67G>A r.(?) p.(Ala23Thr)
?/. - c.67G>A r.(?) p.(Ala23Thr)
?/. - c.81G>T r.(?) p.(Glu27Asp)
+?/. - c.90+13G>A r.(=) p.(=)
-?/. - c.91-896G>A r.(=) p.(=)
?/. - c.91-878A>C r.(=) p.(=)
-?/. - c.91-868C>T r.(=) p.(=)
-?/. - c.104T>C r.(?) p.(Ile35Thr)
-?/. - c.104T>C r.(?) p.(Ile35Thr)
?/. - c.109C>T r.(?) p.(Arg37Cys)
+/. - c.202del r.(?) p.(Leu68TrpfsTer15)
+/. - c.202del r.(?) p.(Leu68Trpfs*15)
?/. - c.223G>A r.(?) p.(Glu75Lys)
-?/. - c.231G>C r.(?) p.(Glu77Asp)
-/. - c.241G>A r.(?) p.(Val81Met)
-/. - c.241G>A r.(?) p.(Val81Met)
-/. - c.241G>A r.(?) p.(Val81Met)
-/. - c.241G>A r.(?) p.(Val81Met)
-?/. - c.264G>A r.(?) p.(Pro88=)
-?/. - c.267G>A r.(?) p.(Arg89=)
-?/. - c.267G>A r.(?) p.(Arg89=)
-?/. - c.267G>A r.(?) p.(Arg89=)
?/. - c.293G>A r.(?) p.(Arg98Gln)
-?/. - c.304G>T r.(?) p.(Val102Leu)
-?/. - c.313-9C>T r.(=) p.(=)
-?/. - c.365G>A r.(?) p.(Arg122Gln)
?/. - c.391T>G r.(?) p.(Phe131Val)
?/. - c.391T>G r.(?) p.(Phe131Val)
?/. - c.394G>A r.(?) p.(Val132Met)
?/. - c.394G>A r.(?) p.(Val132Met)
?/. - c.394G>T r.(?) p.(Val132Leu)
?/. - c.406G>A r.(?) p.(Val136Met)
?/. - c.406G>A r.(?) p.(Val136Met)
-?/. - c.487+3G>A r.spl? p.?
-?/. - c.488-4A>G r.spl? p.?
?/. - c.532C>T r.(?) p.(His178Tyr)
-?/. - c.576G>A r.(?) p.(Pro192=)
-?/. - c.576+6_576+14del r.(=) p.(=)
-?/. - c.576+13C>T r.(=) p.(=)
-?/. - c.577-22C>G r.(=) p.(=)
-/. - c.577-22C>T r.(=) p.(=)
?/. - c.582C>A r.(?) p.(Phe194Leu)
?/. - c.584C>T r.(?) p.(Ser195Leu)
-?/. - c.594G>T r.(?) p.(Val198=)
+/. - c.605G>A r.(?) p.(Arg202His)
+/. - c.605G>A r.(?) p.(Arg202His)
+/. - c.605G>A r.(?) p.(Arg202His)
+/. - c.605G>A r.(?) p.(Arg202His)
+/. - c.605G>A r.(?) p.(Arg202His)
+/. - c.605G>A r.(?) p.(Arg202His)
+/. - c.605G>A r.(?) p.(Arg202His)
+/. - c.605G>A r.(?) p.(Arg202His)
+/. - c.605G>A r.(?) p.(Arg202His)
+/. - c.605G>A r.(605g>a) p.(Arg202His)
?/. - c.605G>A r.(?) p.(Arg202His)
+/. - c.605G>A r.(?) p.(Arg202His)
+?/. - c.605G>A r.(?) p.(Arg202His)
+/. - c.614T>C r.(?) p.(Leu205Pro)
+/. - c.614T>C r.(?) p.(Leu205Pro)
?/. - c.616A>C r.(?) p.(Ile206Leu)
+?/. - c.635A>C r.(?) p.(Gln212Pro)
-?/. - c.644+15C>A r.(=) p.(=)
-?/. - c.645C>T r.(?) p.(His215=)
?/. - c.646G>A r.(?) p.(Gly216Ser)
-?/. - c.684G>A r.(?) p.(Glu228=)
-?/. - c.684G>A r.(?) p.(Glu228=)
-?/. - c.696-3C>T r.spl? p.?
-/. - c.720G>A r.(?) p.(Lys240=)
-/. - c.720G>A r.(?) p.(Lys240=)
-/. - c.720G>A r.(?) p.(Lys240=)
+/. - c.729C>A r.(?) p.(Tyr243*)
+/. - c.733A>C r.(?) p.(Thr245Pro)
+/. - c.848C>T r.(?) p.(Thr283Met)
+/. - c.917G>A r.(?) p.(Arg306His)
?/. - c.923T>G r.(?) p.(Phe308Cys)
-/. - c.977+8C>G r.(=) p.(=)
-/. - c.977+8C>G r.(=) p.(=)
-/. - c.977+8C>G r.(=) p.(=)
+/. - c.983G>T r.(?) p.(Cys328Phe)
?/. - c.1039T>G r.(?) p.(Phe347Val)
?/. - c.1061C>T r.(?) p.(Ala354Val)
+?/. - c.1066C>A r.(?) p.(Leu356Met)
+/. - c.1066C>A r.(?) p.(Leu356Met)
-?/. - c.1069G>A r.(?) p.(Gly357Arg)
?/. - c.1076C>T r.(?) p.(Ser359Leu)
?/. - c.1093A>C r.(?) p.(Lys365Gln)
?/. - c.1102A>T r.(?) p.(Thr368Ser)
?/. - c.1102A>T r.(?) p.(Thr368Ser)
+/. - c.1103C>T r.(?) p.(Thr368Met)
+/. - c.1103C>T r.(?) p.(Thr368Met)
-/. - c.1105-78A>G r.(=) p.(=)
+/. 10i c.1105-24T>A r.[1104_1105ins[1105-36_1105-25;a;1105-23_1105-1],1105_1200del] p.[Thr368_Leu369insLeuSerLeuGlyArgCysCysProAlaSerProGln,Leu369_Leu400del]
-?/. - c.1105-12G>C r.(=) p.(=)
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