Transcript #00014784 (NM_033012.3, TNFSF11 gene)

Transcript name transcript variant 2
Gene name TNFSF11 (tumor necrosis factor (ligand) superfamily, member 11)
Chromosome 13
Transcript - NCBI ID NM_033012.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_143026.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

64 entries on 1 page. Showing entries 1 - 64.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.-1+2672C>G -1 r.(=) p.(=) - intron 2672
./. - c.-1+2691T>C -1 r.(=) p.(=) - intron 2691
./. - c.-1+2691T>C -1 r.(=) p.(=) - intron 2691
./. - c.-1+2691T>C -1 r.(=) p.(=) - intron 2691
./. - c.-1+2691T>C -1 r.(=) p.(=) - intron 2691
./. - c.-1+2691T>C -1 r.(=) p.(=) - intron 2691
./. - c.-1+2691T>C -1 r.(=) p.(=) - intron 2691
./. - c.-1+2691T>C -1 r.(=) p.(=) - intron 2691
./. - c.-1+2691T>C -1 r.(=) p.(=) - intron 2691
./. - c.-1+2691T>C -1 r.(=) p.(=) - intron 2691
./. - c.-1+2691T>C -1 r.(=) p.(=) - intron 2691
./. - c.-1+2691T>C -1 r.(=) p.(=) - intron 2691
./. - c.-1+2691T>C -1 r.(=) p.(=) - intron 2691
./. - c.-1+2691T>C -1 r.(=) p.(=) - intron 2691
./. - c.-1+2691T>C -1 r.(=) p.(=) - intron 2691
./. - c.-1+2691T>C -1 r.(=) p.(=) - intron 2691
./. - c.-1+2691T>C -1 r.(=) p.(=) - intron 2691
./. - c.-1+2691T>C -1 r.(=) p.(=) - intron 2691
./. - c.-1+2691T>C -1 r.(=) p.(=) - intron 2691
./. - c.-1+2691T>C -1 r.(=) p.(=) - intron 2691
./. - c.-1+2691T>C -1 r.(=) p.(=) - intron 2691
./. - c.-1+2691T>C -1 r.(=) p.(=) - intron 2691
./. - c.-1+2691T>C -1 r.(=) p.(=) - intron 2691
./. - c.-1+2691T>C -1 r.(=) p.(=) - intron 2691
./. - c.1-25C>T 1 r.(=) p.(=) - intron 25
./. - c.20C>T 20 r.(?) p.(Ser7Leu) - missense -
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.168+14G>A 168 r.(=) p.(=) - intron 14
./. - c.177A>G 177 r.(?) p.(=) - coding-synonymous -
./. - c.251G>A 251 r.(?) p.(Arg84Lys) - missense -
./. - c.314-34T>A 314 r.(=) p.(=) - intron 34
./. - c.705T>C 705 r.(?) p.(=) - coding-synonymous -
./. - c.705T>C 705 r.(?) p.(=) - coding-synonymous -
./. - c.705T>C 705 r.(?) p.(=) - coding-synonymous -
./. - c.705T>C 705 r.(?) p.(=) - coding-synonymous -
./. - c.*48T>C 783 r.(=) p.(=) - utr-3 -
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