Transcript #00000786 (NM_001243473.1, B9D1 gene)

Transcript name transcript variant 1
Gene name B9D1 (B9 protein domain 1)
Chromosome 17
Transcript - NCBI ID NM_001243473.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001230402.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2013-10-29 10:05:33 +01:00 (CET)
Date last edited N/A


Variants

45 entries on 1 page. Showing entries 1 - 45.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.240C>T 240 r.(?) p.(=) - coding-synonymous -
./. - c.401-35C>T 401 r.(=) p.(=) - intron 35
./. - c.401-35C>T 401 r.(=) p.(=) - intron 35
./. - c.401-35C>T 401 r.(=) p.(=) - intron 35
./. - c.401-35C>T 401 r.(=) p.(=) - intron 35
./. - c.401-35C>T 401 r.(=) p.(=) - intron 35
./. - c.401-35C>T 401 r.(=) p.(=) - intron 35
./. - c.401-35C>T 401 r.(=) p.(=) - intron 35
./. - c.401-35C>T 401 r.(=) p.(=) - intron 35
./. - c.401-35C>T 401 r.(=) p.(=) - intron 35
./. - c.401-35C>T 401 r.(=) p.(=) - intron 35
./. - c.401-35C>T 401 r.(=) p.(=) - intron 35
./. - c.401-35C>T 401 r.(=) p.(=) - intron 35
./. - c.401-35C>T 401 r.(=) p.(=) - intron 35
./. - c.401-35C>T 401 r.(=) p.(=) - intron 35
./. - c.401-35C>T 401 r.(=) p.(=) - intron 35
./. - c.401-35C>T 401 r.(=) p.(=) - intron 35
./. - c.401-35C>T 401 r.(=) p.(=) - intron 35
./. - c.401-35C>T 401 r.(=) p.(=) - intron 35
./. - c.401-35C>T 401 r.(=) p.(=) - intron 35
./. - c.401-35C>T 401 r.(=) p.(=) - intron 35
./. - c.463+29C>G 463 r.(=) p.(=) - intron 29
./. - c.559C>T 559 r.(?) p.(His187Tyr) - missense -
./. - c.559C>T 559 r.(?) p.(His187Tyr) - missense -
./. - c.559C>T 559 r.(?) p.(His187Tyr) - missense -
./. - c.559C>T 559 r.(?) p.(His187Tyr) - missense -
./. - c.559C>T 559 r.(?) p.(His187Tyr) - missense -
./. - c.559C>T 559 r.(?) p.(His187Tyr) - missense -
./. - c.559C>T 559 r.(?) p.(His187Tyr) - missense -
./. - c.559C>T 559 r.(?) p.(His187Tyr) - missense -
./. - c.559C>T 559 r.(?) p.(His187Tyr) - missense -
./. - c.559C>T 559 r.(?) p.(His187Tyr) - missense -
./. - c.559C>T 559 r.(?) p.(His187Tyr) - missense -
./. - c.559C>T 559 r.(?) p.(His187Tyr) - missense -
./. - c.559C>T 559 r.(?) p.(His187Tyr) - missense -
./. - c.559C>T 559 r.(?) p.(His187Tyr) - missense -
./. - c.559C>T 559 r.(?) p.(His187Tyr) - missense -
./. - c.559C>T 559 r.(?) p.(His187Tyr) - missense -
./. - c.559C>T 559 r.(?) p.(His187Tyr) - missense -
./. - c.559C>T 559 r.(?) p.(His187Tyr) - missense -
./. - c.559C>T 559 r.(?) p.(His187Tyr) - missense -
./. - c.559C>T 559 r.(?) p.(His187Tyr) - missense -
./. - c.559C>T 559 r.(?) p.(His187Tyr) - missense -
./. - c.559C>T 559 r.(?) p.(His187Tyr) - missense -
./. - c.767A>G 767 r.(?) p.(Tyr256Cys) - missense -
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