Transcript #00007123 (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 2013-10-30 12:53:40 +01:00 (CET)
Date last edited N/A


Variants

525 entries on 6 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.68-26T>C 68 r.(=) p.(=) - intron 26
./. - c.199G>A 199 r.(?) p.(Gly67Ser) - missense -
./. - c.353C>T 353 r.(?) p.(Pro118Leu) - missense -
./. - c.478+15G>A 478 r.(=) p.(=) - intron 15
./. - c.478+15G>A 478 r.(=) p.(=) - intron 15
./. - c.478+15G>A 478 r.(=) p.(=) - intron 15
./. - c.479-32T>C 479 r.(=) p.(=) - intron 32
./. - c.479-32T>C 479 r.(=) p.(=) - intron 32
./. - c.537A>G 537 r.(?) p.(=) - coding-synonymous -
./. - c.1332C>T 1332 r.(?) p.(=) - coding-synonymous -
./. - c.1543C>G 1543 r.(?) p.(Gln515Glu) - missense -
./. - c.1543C>G 1543 r.(?) p.(Gln515Glu) - missense -
./. - c.1890A>G 1890 r.(?) p.(=) - coding-synonymous -
./. - c.1890A>G 1890 r.(?) p.(=) - coding-synonymous -
./. - c.2200T>G 2200 r.(?) p.(Ser734Ala) - missense -
./. - c.2200T>G 2200 r.(?) p.(Ser734Ala) - missense -
./. - c.2200T>G 2200 r.(?) p.(Ser734Ala) - missense -
./. - c.2200T>G 2200 r.(?) p.(Ser734Ala) - missense -
./. - c.2200T>G 2200 r.(?) p.(Ser734Ala) - missense -
./. - c.2200T>G 2200 r.(?) p.(Ser734Ala) - missense -
./. - c.2200T>G 2200 r.(?) p.(Ser734Ala) - missense -
./. - c.2200T>G 2200 r.(?) p.(Ser734Ala) - missense -
./. - c.2200T>G 2200 r.(?) p.(Ser734Ala) - missense -
./. - c.2200T>G 2200 r.(?) p.(Ser734Ala) - missense -
./. - c.2200T>G 2200 r.(?) p.(Ser734Ala) - missense -
./. - c.2200T>G 2200 r.(?) p.(Ser734Ala) - missense -
./. - c.2200T>G 2200 r.(?) p.(Ser734Ala) - missense -
./. - c.2200T>G 2200 r.(?) p.(Ser734Ala) - missense -
./. - c.2200T>G 2200 r.(?) p.(Ser734Ala) - missense -
./. - c.2200T>G 2200 r.(?) p.(Ser734Ala) - missense -
./. - c.2200T>G 2200 r.(?) p.(Ser734Ala) - missense -
./. - c.2200T>G 2200 r.(?) p.(Ser734Ala) - missense -
./. - c.2200T>G 2200 r.(?) p.(Ser734Ala) - missense -
./. - c.2200T>G 2200 r.(?) p.(Ser734Ala) - missense -
./. - c.2200T>G 2200 r.(?) p.(Ser734Ala) - missense -
./. - c.2200T>G 2200 r.(?) p.(Ser734Ala) - missense -
./. - c.2200T>G 2200 r.(?) p.(Ser734Ala) - missense -
./. - c.2200T>G 2200 r.(?) p.(Ser734Ala) - missense -
./. - c.2334T>C 2334 r.(?) p.(=) - coding-synonymous -
./. - c.2334T>C 2334 r.(?) p.(=) - coding-synonymous -
./. - c.2334T>C 2334 r.(?) p.(=) - coding-synonymous -
./. - c.2334T>C 2334 r.(?) p.(=) - coding-synonymous -
./. - c.2334T>C 2334 r.(?) p.(=) - coding-synonymous -
./. - c.2334T>C 2334 r.(?) p.(=) - coding-synonymous -
./. - c.2334T>C 2334 r.(?) p.(=) - coding-synonymous -
./. - c.2334T>C 2334 r.(?) p.(=) - coding-synonymous -
./. - c.2334T>C 2334 r.(?) p.(=) - coding-synonymous -
./. - c.2334T>C 2334 r.(?) p.(=) - coding-synonymous -
./. - c.2334T>C 2334 r.(?) p.(=) - coding-synonymous -
./. - c.2334T>C 2334 r.(?) p.(=) - coding-synonymous -
./. - c.2334T>C 2334 r.(?) p.(=) - coding-synonymous -
./. - c.2334T>C 2334 r.(?) p.(=) - coding-synonymous -
./. - c.2334T>C 2334 r.(?) p.(=) - coding-synonymous -
./. - c.2334T>C 2334 r.(?) p.(=) - coding-synonymous -
./. - c.2334T>C 2334 r.(?) p.(=) - coding-synonymous -
./. - c.2334T>C 2334 r.(?) p.(=) - coding-synonymous -
./. - c.2334T>C 2334 r.(?) p.(=) - coding-synonymous -
./. - c.2334T>C 2334 r.(?) p.(=) - coding-synonymous -
./. - c.2443G>A 2443 r.(?) p.(Gly815Arg) - missense -
./. - c.2443G>A 2443 r.(?) p.(Gly815Arg) - missense -
./. - c.2443G>A 2443 r.(?) p.(Gly815Arg) - missense -
./. - c.2443G>A 2443 r.(?) p.(Gly815Arg) - missense -
./. - c.2443G>A 2443 r.(?) p.(Gly815Arg) - missense -
./. - c.2561G>A 2561 r.(?) p.(Arg854Gln) - missense -
./. - c.2610G>T 2610 r.(?) p.(Gln870His) - missense -
./. - c.2761+11G>T 2761 r.(=) p.(=) - intron 11
./. - c.2761+11G>T 2761 r.(=) p.(=) - intron 11
./. - c.2761+14T>C 2761 r.(=) p.(=) - intron 14
./. - c.2761+14T>C 2761 r.(=) p.(=) - intron 14
./. - c.2761+14T>C 2761 r.(=) p.(=) - intron 14
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