Transcript #00009326 (NM_001033604.1, BBS9 gene)

Transcript name transcript variant 3
Gene name BBS9 (Bardet-Biedl syndrome 9)
Chromosome 7
Transcript - NCBI ID NM_001033604.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001028776.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2014-01-21 10:30:20 +01:00 (CET)
Date last edited N/A


Variants

58 entries on 1 page. Showing entries 1 - 58.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.34A>G 34 r.(?) p.(Thr12Ala) - missense -
./. - c.263+39A>G 263 r.(=) p.(=) - intron 39
./. - c.263+39A>G 263 r.(=) p.(=) - intron 39
./. - c.263+39A>G 263 r.(=) p.(=) - intron 39
./. - c.263+39A>G 263 r.(=) p.(=) - intron 39
./. - c.263+39A>G 263 r.(=) p.(=) - intron 39
./. - c.263+39A>G 263 r.(=) p.(=) - intron 39
./. - c.263+39A>G 263 r.(=) p.(=) - intron 39
./. - c.263+39A>G 263 r.(=) p.(=) - intron 39
./. - c.328+22G>A 328 r.(=) p.(=) - intron 22
./. - c.861A>C 861 r.(?) p.(=) - coding-synonymous -
./. - c.861A>C 861 r.(?) p.(=) - coding-synonymous -
./. - c.1017-6T>C 1017 r.(=) p.(=) - splice 6
./. - c.1017-6T>C 1017 r.(=) p.(=) - splice 6
./. - c.1017-6T>C 1017 r.(=) p.(=) - splice 6
./. - c.1029A>G 1029 r.(?) p.(=) - coding-synonymous -
./. - c.1029A>G 1029 r.(?) p.(=) - coding-synonymous -
./. - c.1029A>G 1029 r.(?) p.(=) - coding-synonymous -
./. - c.1246G>A 1246 r.(?) p.(Val416Met) - missense -
./. - c.1275+13G>T 1275 r.(=) p.(=) - intron 13
./. - c.1275+13G>T 1275 r.(=) p.(=) - intron 13
./. - c.1275+13G>T 1275 r.(=) p.(=) - intron 13
./. - c.1275+13G>T 1275 r.(=) p.(=) - intron 13
./. - c.1275+13G>T 1275 r.(=) p.(=) - intron 13
./. - c.1275+13G>T 1275 r.(=) p.(=) - intron 13
./. - c.1275+13G>T 1275 r.(=) p.(=) - intron 13
./. - c.1275+13G>T 1275 r.(=) p.(=) - intron 13
./. - c.1275+13G>T 1275 r.(=) p.(=) - intron 13
./. - c.1275+13G>T 1275 r.(=) p.(=) - intron 13
./. - c.1275+13G>T 1275 r.(=) p.(=) - intron 13
./. - c.1275+13G>T 1275 r.(=) p.(=) - intron 13
./. - c.1275+28G>T 1275 r.(=) p.(=) - intron 28
./. - c.1363G>A 1363 r.(?) p.(Ala455Thr) - missense -
./. - c.1363G>A 1363 r.(?) p.(Ala455Thr) - missense -
./. - c.1363G>A 1363 r.(?) p.(Ala455Thr) - missense -
./. - c.1363G>A 1363 r.(?) p.(Ala455Thr) - missense -
./. - c.1363G>A 1363 r.(?) p.(Ala455Thr) - missense -
./. - c.1363G>A 1363 r.(?) p.(Ala455Thr) - missense -
./. - c.1363G>A 1363 r.(?) p.(Ala455Thr) - missense -
./. - c.1363G>A 1363 r.(?) p.(Ala455Thr) - missense -
./. - c.1363G>A 1363 r.(?) p.(Ala455Thr) - missense -
./. - c.1363G>A 1363 r.(?) p.(Ala455Thr) - missense -
./. - c.1363G>A 1363 r.(?) p.(Ala455Thr) - missense -
./. - c.1363G>A 1363 r.(?) p.(Ala455Thr) - missense -
./. - c.1363G>A 1363 r.(?) p.(Ala455Thr) - missense -
./. - c.1432+47T>A 1432 r.(=) p.(=) - intron 47
./. - c.1432+47T>A 1432 r.(=) p.(=) - intron 47
./. - c.1432+47T>A 1432 r.(=) p.(=) - intron 47
./. - c.1432+47T>A 1432 r.(=) p.(=) - intron 47
./. - c.1432+47T>A 1432 r.(=) p.(=) - intron 47
./. - c.1432+47T>A 1432 r.(=) p.(=) - intron 47
./. - c.1432+47T>A 1432 r.(=) p.(=) - intron 47
./. - c.1432+47T>A 1432 r.(=) p.(=) - intron 47
./. - c.1432+47T>A 1432 r.(=) p.(=) - intron 47
./. - c.1432+47T>A 1432 r.(=) p.(=) - intron 47
./. - c.1441C>A 1441 r.(?) p.(Pro481Thr) - missense -
./. - c.1744A>C 1744 r.(?) p.(Ile582Leu) - missense -
./. - c.2194-20A>C 2194 r.(=) p.(=) - intron 20
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