Transcript #00009392 (NM_001256856.1, BTRC gene)

Transcript name transcript variant 3
Gene name BTRC (beta-transducin repeat containing E3 ubiquitin protein ligase)
Chromosome 10
Transcript - NCBI ID NM_001256856.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001243785.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2014-01-21 10:36:06 +01:00 (CET)
Date last edited N/A


Variants

44 entries on 1 page. Showing entries 1 - 44.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.478+7C>G 478 r.(=) p.(=) - splice 7
./. - c.478+7C>G 478 r.(=) p.(=) - splice 7
./. - c.478+7C>G 478 r.(=) p.(=) - splice 7
./. - c.478+7C>G 478 r.(=) p.(=) - splice 7
./. - c.478+7C>G 478 r.(=) p.(=) - splice 7
./. - c.478+7C>G 478 r.(=) p.(=) - splice 7
./. - c.478+7C>G 478 r.(=) p.(=) - splice 7
./. - c.478+7C>G 478 r.(=) p.(=) - splice 7
./. - c.478+7C>G 478 r.(=) p.(=) - splice 7
./. - c.478+7C>G 478 r.(=) p.(=) - splice 7
./. - c.478+7C>G 478 r.(=) p.(=) - splice 7
./. - c.478+7C>G 478 r.(=) p.(=) - splice 7
./. - c.478+7C>G 478 r.(=) p.(=) - splice 7
./. - c.478+7C>G 478 r.(=) p.(=) - splice 7
./. - c.478+7C>G 478 r.(=) p.(=) - splice 7
./. - c.478+7C>G 478 r.(=) p.(=) - splice 7
./. - c.478+7C>G 478 r.(=) p.(=) - splice 7
./. - c.478+7C>G 478 r.(=) p.(=) - splice 7
./. - c.478+7C>G 478 r.(=) p.(=) - splice 7
./. - c.478+7C>G 478 r.(=) p.(=) - splice 7
./. - c.478+7C>G 478 r.(=) p.(=) - splice 7
./. - c.478+49G>A 478 r.(=) p.(=) - intron 49
./. - c.478+49G>A 478 r.(=) p.(=) - intron 49
./. - c.478+49G>A 478 r.(=) p.(=) - intron 49
./. - c.478+49G>A 478 r.(=) p.(=) - intron 49
./. - c.478+49G>A 478 r.(=) p.(=) - intron 49
./. - c.478+49G>A 478 r.(=) p.(=) - intron 49
./. - c.478+49G>A 478 r.(=) p.(=) - intron 49
./. - c.478+49G>A 478 r.(=) p.(=) - intron 49
./. - c.478+49G>A 478 r.(=) p.(=) - intron 49
./. - c.478+49G>A 478 r.(=) p.(=) - intron 49
./. - c.478+49G>A 478 r.(=) p.(=) - intron 49
./. - c.478+49G>A 478 r.(=) p.(=) - intron 49
./. - c.478+49G>A 478 r.(=) p.(=) - intron 49
./. - c.478+49G>A 478 r.(=) p.(=) - intron 49
./. - c.478+49G>A 478 r.(=) p.(=) - intron 49
./. - c.478+49G>A 478 r.(=) p.(=) - intron 49
./. - c.478+49G>A 478 r.(=) p.(=) - intron 49
./. - c.478+49G>A 478 r.(=) p.(=) - intron 49
./. - c.609C>T 609 r.(?) p.(=) - coding-synonymous -
./. - c.609C>T 609 r.(?) p.(=) - coding-synonymous -
./. - c.609C>T 609 r.(?) p.(=) - coding-synonymous -
./. - c.1549G>T 1549 r.(?) p.(Ala517Ser) - missense -
./. - c.1697C>A 1697 r.(?) p.(Pro566His) - missense -
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