Transcript #00000421 (NM_003235.4, TG gene)

Transcript name thyroglobulin
Gene name TG (thyroglobulin)
Chromosome 8
Transcript - NCBI ID NM_003235.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_003226.4
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2012-09-13 12:13:48 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.83C>T r.(?) p.(Ala28Val)
?/. - c.94C>T r.(?) p.(Arg32Cys)
-/. - c.144C>T r.(?) p.(Tyr48=)
-?/. - c.199G>A r.(?) p.(Gly67Ser)
+?/. - c.211del r.(?) p.(Trp71GlyfsTer35)
+?/. - c.229G>A r.(?) p.(Gly77Ser)
+/. - c.229G>A r.(?) p.(Gly77Ser)
+?/. - c.229G>A r.(?) p.(Gly77Ser)
+/. - c.229G>A r.(?) p.(Gly77Ser)
?/. - c.262C>T r.(?) p.(Arg88Trp)
?/. - c.275G>T r.(?) p.(Cys92Phe)
?/. - c.275G>T r.(?) p.(Cys92Phe)
-?/. - c.325A>G r.(?) p.(Ile109Val)
-?/. - c.325A>G r.(?) p.(Ile109Val)
-?/. - c.353C>T r.(?) p.(Pro118Leu)
+/. - c.416G>A r.(?) p.(Trp139Ter)
?/. - c.455G>A r.(?) p.(Arg152His)
-?/. - c.455G>A r.(?) p.(Arg152His)
-/. - c.478+15G>A r.(=) p.(=)
-/. - c.478+16C>T r.(=) p.(=)
+?/. - c.479-1G>T r.(?) p.(?)
+/. - c.492T>A r.(?) p.(Cys164*)
-/. - c.555G>A r.(?) p.(Ala185=)
+/. - c.638+5G>A r.spl? p.?
-/. - c.762G>A r.(?) p.(Leu254=)
-?/. - c.848G>A r.(?) p.(Arg283Gln)
-?/. - c.855C>T r.(?) p.(Leu285=)
+/. - c.886C>T r.(?) p.(Arg296Ter)
?/. - c.890-13G>A r.(=) p.(=)
-/. - c.1075+8T>G r.(=) p.(=)
?/. - c.1267C>T r.(?) p.(Arg423Cys)
-/. - c.1332C>T r.(?) p.(Ile444=)
+/. - c.1348del r.(?) p.(Ser450Profs*29)
+/. - c.1351C>T r.(?) p.(Arg451Ter)
-?/. - c.1434G>A r.(?) p.(Val478=)
+/. - c.1507C>T r.(?) p.(Gln503Ter)
-/. - c.1543C>G r.(?) p.(Gln515Glu)
?/. - c.1567T>C r.(?) p.(Ser523Pro)
-?/. - c.1573G>A r.(?) p.(Gly525Arg)
-?/. - c.1573G>A r.(?) p.(Gly525Arg)
-?/. - c.1628C>G r.(?) p.(Thr543Ser)
?/. - c.1775C>T r.(?) p.(Ala592Val)
-/. - c.1821C>T r.(?) p.(Thr607=)
+/. - c.1831_1841del r.(?) p.(Thr611AlafsTer13)
-?/. - c.1834C>A r.(?) p.(Pro612Thr)
?/. - c.1862C>T r.(?) p.(Thr621Met)
-?/. - c.1863G>A r.(?) p.(Thr621=)
-/. - c.1890A>G r.(?) p.(Gln630=)
-?/. - c.1900G>A r.(?) p.(Gly634Arg)
?/. - c.1911G>T r.(?) p.(Trp637Cys)
+?/. - c.1911G>T r.(?) p.(Trp637Cys)
-?/. - c.1958G>A r.(?) p.(Gly653Asp)
+/. - c.2103dup r.(?) p.(Glu702ArgfsTer6)
+/. - c.2149C>T r.(?) p.(Arg717*)
-/. - c.2200T>G r.(?) p.(Ser734Ala)
-/. - c.2200T>G r.(?) p.(Ser734Ala)
?/. - c.2246C>G r.(?) p.(Ser749Cys)
?/. - c.2276A>G r.(?) p.(Tyr759Cys)
-?/. - c.2304G>A r.(?) p.(Gln768=)
+?/. - c.2311C>T r.(?) p.(Gln771Ter)
-/. - c.2334T>C r.(?) p.(Pro778=)
-/. - c.2334T>C r.(?) p.(Pro778=)
+/. - c.2338C>T r.(?) p.(Gln780Ter)
-?/. - c.2443G>A r.(?) p.(Gly815Arg)
-/. - c.2443G>A r.(?) p.(Gly815Arg)
-?/. - c.2443G>A r.(?) p.(Gly815Arg)
-/. - c.2520T>C r.(?) p.(Pro840=)
-?/. - c.2610G>T r.(?) p.(Gln870His)
-?/. - c.2610G>T r.(?) p.(Gln870His)
?/. - c.2610G>T r.(?) p.(Gln870His)
?/. - c.2610G>T r.(?) p.(Gln870His)
?/. - c.2610G>T r.(?) p.(Gln870His)
-/. - c.2652A>C r.(?) p.(Ser884=)
-?/. - c.2652A>C r.(?) p.(Ser884=)
+/. - c.2744_2748del r.(?) p.(Pro915Glnfs*10)
-/. - c.2761+11G>T r.(=) p.(=)
-/. - c.2761+14T>C r.(=) p.(=)
?/. - c.2819A>C r.(?) p.(Glu940Ala)
?/. - c.2930C>T r.(?) p.(Pro977Leu)
-?/. - c.2963G>A r.(?) p.(Arg988His)
-/. - c.2963G>C r.(?) p.(Arg988Pro)
-?/. - c.2980A>G r.(?) p.(Ile994Val)
-/. - c.3001+19A>G r.(=) p.(=)
-?/. - c.3024C>T r.(?) p.(Arg1008=)
-/. - c.3030T>C r.(?) p.(Phe1010=)
-?/. - c.3035C>T r.(?) p.(Pro1012Leu)
-?/. - c.3039C>T r.(?) p.(Asp1013=)
-/. - c.3039C>T r.(?) p.(Asp1013=)
-/. - c.3057C>T r.(?) p.(Ser1019=)
-?/. - c.3057C>T r.(?) p.(Ser1019=)
?/. - c.3068G>C r.(?) p.(Arg1023Pro)
-/. - c.3082A>G r.(?) p.(Met1028Val)
-/. - c.3082A>G r.(?) p.(Met1028Val)
-/. - c.3129C>T r.(?) p.(His1043=)
-/. - c.3139+9G>A r.(=) p.(=)
-?/. - c.3140-19C>T r.(=) p.(=)
-/. - c.3187C>A r.(?) p.(Leu1063Met)
-?/. - c.3187C>A r.(?) p.(Leu1063Met)
-/. - c.3217+11A>C r.(=) p.(=)
-/. - c.3313G>A r.(?) p.(Val1105Ile)
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