Transcript #00000863 (NM_001143810.1, BDNF gene)

Transcript name transcript variant 18
Gene name BDNF (brain-derived neurotrophic factor)
Chromosome 11
Transcript - NCBI ID NM_001143810.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001137282.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2013-10-29 10:13:50 +01:00 (CET)
Date last edited N/A


Variants

51 entries on 1 page. Showing entries 1 - 51.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.-179G>A -179 r.(=) p.(=) - utr-5 -
./. - c.-59+1535G>A -59 r.(=) p.(=) - intron 1535
./. - c.-59+1581G>A -59 r.(=) p.(=) - intron 1581
./. - c.-59+1710G>A -59 r.(=) p.(=) - intron 1710
./. - c.-59+1710G>A -59 r.(=) p.(=) - intron 1710
./. - c.-59+1710G>A -59 r.(=) p.(=) - intron 1710
./. - c.-38A>G -38 r.(=) p.(=) - utr-5 -
./. - c.442G>A 442 r.(?) p.(Val148Met) - missense -
./. - c.442G>A 442 r.(?) p.(Val148Met) - missense -
./. - c.442G>A 442 r.(?) p.(Val148Met) - missense -
./. - c.442G>A 442 r.(?) p.(Val148Met) - missense -
./. - c.442G>A 442 r.(?) p.(Val148Met) - missense -
./. - c.442G>A 442 r.(?) p.(Val148Met) - missense -
./. - c.442G>A 442 r.(?) p.(Val148Met) - missense -
./. - c.442G>A 442 r.(?) p.(Val148Met) - missense -
./. - c.442G>A 442 r.(?) p.(Val148Met) - missense -
./. - c.442G>A 442 r.(?) p.(Val148Met) - missense -
./. - c.442G>A 442 r.(?) p.(Val148Met) - missense -
./. - c.442G>A 442 r.(?) p.(Val148Met) - missense -
./. - c.442G>A 442 r.(?) p.(Val148Met) - missense -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
./. - c.696A>G 696 r.(?) p.(=) - coding-synonymous -
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