Transcript #00007918 (NM_001127208.2, TET2 gene)

Transcript name tet oncogene family member 2, transcript variant 1
Gene name TET2 (tet methylcytosine dioxygenase 2)
Chromosome 4
Transcript - NCBI ID NM_001127208.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001120680.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2013-10-30 14:11:46 +01:00 (CET)
Date last edited N/A


Variants

59 entries on 1 page. Showing entries 1 - 59.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.9G>A 9 r.(?) p.(=) - coding-synonymous -
./. - c.86C>G 86 r.(?) p.(Pro29Arg) - missense -
./. - c.86C>G 86 r.(?) p.(Pro29Arg) - missense -
./. - c.86C>G 86 r.(?) p.(Pro29Arg) - missense -
./. - c.86C>G 86 r.(?) p.(Pro29Arg) - missense -
./. - c.86C>G 86 r.(?) p.(Pro29Arg) - missense -
./. - c.86C>G 86 r.(?) p.(Pro29Arg) - missense -
./. - c.652G>A 652 r.(?) p.(Val218Met) - missense -
./. - c.652G>A 652 r.(?) p.(Val218Met) - missense -
./. - c.652G>A 652 r.(?) p.(Val218Met) - missense -
./. - c.1088C>T 1088 r.(?) p.(Pro363Leu) - missense -
./. - c.1088C>T 1088 r.(?) p.(Pro363Leu) - missense -
./. - c.1088C>T 1088 r.(?) p.(Pro363Leu) - missense -
./. - c.1884G>A 1884 r.(?) p.(=) - coding-synonymous -
./. - c.2604T>G 2604 r.(?) p.(Phe868Leu) - missense -
./. - c.3090G>A 3090 r.(?) p.(=) - coding-synonymous -
./. - c.3117G>A 3117 r.(?) p.(=) - coding-synonymous -
./. - c.3117G>A 3117 r.(?) p.(=) - coding-synonymous -
./. - c.3117G>A 3117 r.(?) p.(=) - coding-synonymous -
./. - c.3117G>A 3117 r.(?) p.(=) - coding-synonymous -
./. - c.3117G>A 3117 r.(?) p.(=) - coding-synonymous -
./. - c.3117G>A 3117 r.(?) p.(=) - coding-synonymous -
./. - c.3117G>A 3117 r.(?) p.(=) - coding-synonymous -
./. - c.3117G>A 3117 r.(?) p.(=) - coding-synonymous -
./. - c.3117G>A 3117 r.(?) p.(=) - coding-synonymous -
./. - c.3803+45G>A 3803 r.(=) p.(=) - intron 45
./. - c.3803+45G>A 3803 r.(=) p.(=) - intron 45
./. - c.3803+45G>A 3803 r.(=) p.(=) - intron 45
./. - c.4045-35C>A 4045 r.(=) p.(=) - intron 35
./. - c.4045-35C>A 4045 r.(=) p.(=) - intron 35
./. - c.4045-35C>A 4045 r.(=) p.(=) - intron 35
./. - c.4045-35C>A 4045 r.(=) p.(=) - intron 35
./. - c.4045-27G>A 4045 r.(=) p.(=) - intron 27
./. - c.4140T>C 4140 r.(?) p.(=) - coding-synonymous -
./. - c.4140T>C 4140 r.(?) p.(=) - coding-synonymous -
./. - c.4140T>C 4140 r.(?) p.(=) - coding-synonymous -
./. - c.4140T>C 4140 r.(?) p.(=) - coding-synonymous -
./. - c.4140T>C 4140 r.(?) p.(=) - coding-synonymous -
./. - c.5162T>G 5162 r.(?) p.(Leu1721Trp) - missense -
./. - c.5162T>G 5162 r.(?) p.(Leu1721Trp) - missense -
./. - c.5162T>G 5162 r.(?) p.(Leu1721Trp) - missense -
./. - c.5162T>G 5162 r.(?) p.(Leu1721Trp) - missense -
./. - c.5284A>G 5284 r.(?) p.(Ile1762Val) - missense -
./. - c.5284A>G 5284 r.(?) p.(Ile1762Val) - missense -
./. - c.5284A>G 5284 r.(?) p.(Ile1762Val) - missense -
./. - c.5284A>G 5284 r.(?) p.(Ile1762Val) - missense -
./. - c.5284A>G 5284 r.(?) p.(Ile1762Val) - missense -
./. - c.5284A>G 5284 r.(?) p.(Ile1762Val) - missense -
./. - c.5284A>G 5284 r.(?) p.(Ile1762Val) - missense -
./. - c.5284A>G 5284 r.(?) p.(Ile1762Val) - missense -
./. - c.5284A>G 5284 r.(?) p.(Ile1762Val) - missense -
./. - c.5284A>G 5284 r.(?) p.(Ile1762Val) - missense -
./. - c.5284A>G 5284 r.(?) p.(Ile1762Val) - missense -
./. - c.5284A>G 5284 r.(?) p.(Ile1762Val) - missense -
./. - c.5284A>G 5284 r.(?) p.(Ile1762Val) - missense -
./. - c.5284A>G 5284 r.(?) p.(Ile1762Val) - missense -
./. - c.5333A>G 5333 r.(?) p.(His1778Arg) - missense -
./. - c.5333A>G 5333 r.(?) p.(His1778Arg) - missense -
./. - c.5449C>A 5449 r.(?) p.(His1817Asn) - missense -
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