Transcript #00009219 (NM_001206524.1, CASP10 gene)

Transcript name transcript variant 6
Gene name CASP10 (caspase 10, apoptosis-related cysteine peptidase)
Chromosome 2
Transcript - NCBI ID NM_001206524.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001193453.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2014-01-21 10:26:21 +01:00 (CET)
Date last edited N/A


Variants

61 entries on 1 page. Showing entries 1 - 61.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.-7-17C>T -7 r.(=) p.(=) - intron 17
./. - c.177A>G 177 r.(?) p.(=) - coding-synonymous -
./. - c.177A>G 177 r.(?) p.(=) - coding-synonymous -
./. - c.177A>G 177 r.(?) p.(=) - coding-synonymous -
./. - c.177A>G 177 r.(?) p.(=) - coding-synonymous -
./. - c.177A>G 177 r.(?) p.(=) - coding-synonymous -
./. - c.177A>G 177 r.(?) p.(=) - coding-synonymous -
./. - c.177A>G 177 r.(?) p.(=) - coding-synonymous -
./. - c.177A>G 177 r.(?) p.(=) - coding-synonymous -
./. - c.177A>G 177 r.(?) p.(=) - coding-synonymous -
./. - c.177A>G 177 r.(?) p.(=) - coding-synonymous -
./. - c.177A>G 177 r.(?) p.(=) - coding-synonymous -
./. - c.177A>G 177 r.(?) p.(=) - coding-synonymous -
./. - c.177A>G 177 r.(?) p.(=) - coding-synonymous -
./. - c.177A>G 177 r.(?) p.(=) - coding-synonymous -
./. - c.177A>G 177 r.(?) p.(=) - coding-synonymous -
./. - c.177A>G 177 r.(?) p.(=) - coding-synonymous -
./. - c.177A>G 177 r.(?) p.(=) - coding-synonymous -
./. - c.177A>G 177 r.(?) p.(=) - coding-synonymous -
./. - c.177A>G 177 r.(?) p.(=) - coding-synonymous -
./. - c.177A>G 177 r.(?) p.(=) - coding-synonymous -
./. - c.177A>G 177 r.(?) p.(=) - coding-synonymous -
./. - c.177A>G 177 r.(?) p.(=) - coding-synonymous -
./. - c.177A>G 177 r.(?) p.(=) - coding-synonymous -
./. - c.347+8C>T 347 r.(=) p.(=) - splice 8
./. - c.347+9G>T 347 r.(=) p.(=) - intron 9
./. - c.347+9G>T 347 r.(=) p.(=) - intron 9
./. - c.347+9G>T 347 r.(=) p.(=) - intron 9
./. - c.685-20C>T 685 r.(=) p.(=) - intron 20
./. - c.685-20C>T 685 r.(=) p.(=) - intron 20
./. - c.722-3C>T 722 r.spl? p.? - splice 3
./. - c.722-3C>T 722 r.spl? p.? - splice 3
./. - c.722-3C>T 722 r.spl? p.? - splice 3
./. - c.722-3C>T 722 r.spl? p.? - splice 3
./. - c.722-3C>T 722 r.spl? p.? - splice 3
./. - c.722-3C>T 722 r.spl? p.? - splice 3
./. - c.1027G>A 1027 r.(?) p.(Val343Ile) - missense -
./. - c.1027G>A 1027 r.(?) p.(Val343Ile) - missense -
./. - c.1214+18T>A 1214 r.(=) p.(=) - intron 18
./. - c.1214+33T>G 1214 r.(=) p.(=) - intron 33
./. - c.1363T>A 1363 r.(?) p.(Leu455Ile) - missense -
./. - c.1363T>A 1363 r.(?) p.(Leu455Ile) - missense -
./. - c.1363T>A 1363 r.(?) p.(Leu455Ile) - missense -
./. - c.1363T>A 1363 r.(?) p.(Leu455Ile) - missense -
./. - c.1363T>A 1363 r.(?) p.(Leu455Ile) - missense -
./. - c.1363T>A 1363 r.(?) p.(Leu455Ile) - missense -
./. - c.1363T>A 1363 r.(?) p.(Leu455Ile) - missense -
./. - c.1363T>A 1363 r.(?) p.(Leu455Ile) - missense -
./. - c.1363T>A 1363 r.(?) p.(Leu455Ile) - missense -
./. - c.1363T>A 1363 r.(?) p.(Leu455Ile) - missense -
./. - c.1363T>A 1363 r.(?) p.(Leu455Ile) - missense -
./. - c.1363T>A 1363 r.(?) p.(Leu455Ile) - missense -
./. - c.1363T>A 1363 r.(?) p.(Leu455Ile) - missense -
./. - c.1363T>A 1363 r.(?) p.(Leu455Ile) - missense -
./. - c.1363T>A 1363 r.(?) p.(Leu455Ile) - missense -
./. - c.1363T>A 1363 r.(?) p.(Leu455Ile) - missense -
./. - c.1363T>A 1363 r.(?) p.(Leu455Ile) - missense -
./. - c.1363T>A 1363 r.(?) p.(Leu455Ile) - missense -
./. - c.1363T>A 1363 r.(?) p.(Leu455Ile) - missense -
./. - c.1363T>A 1363 r.(?) p.(Leu455Ile) - missense -
./. - c.1363T>A 1363 r.(?) p.(Leu455Ile) - missense -
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