Transcript #00007887 (NM_001195141.1, TCOF1 gene)

Transcript name transcript variant 7
Gene name TCOF1 (Treacher Collins-Franceschetti syndrome 1)
Chromosome 5
Transcript - NCBI ID NM_001195141.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001182070.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2013-10-30 14:08:56 +01:00 (CET)
Date last edited N/A


Variants

93 entries on 1 page. Showing entries 1 - 93.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.109-13T>C 109 r.(=) p.(=) - intron 13
./. - c.295G>A 295 r.(?) p.(Ala99Thr) - missense -
./. - c.1083+39G>A 1083 r.(=) p.(=) - intron 39
./. - c.1083+39G>A 1083 r.(=) p.(=) - intron 39
./. - c.1281G>A 1281 r.(?) p.(=) - coding-synonymous-near-splice -
./. - c.1578C>T 1578 r.(?) p.(=) - coding-synonymous -
./. - c.1578C>T 1578 r.(?) p.(=) - coding-synonymous -
./. - c.1578C>T 1578 r.(?) p.(=) - coding-synonymous -
./. - c.1578C>T 1578 r.(?) p.(=) - coding-synonymous -
./. - c.1578C>T 1578 r.(?) p.(=) - coding-synonymous -
./. - c.1578C>T 1578 r.(?) p.(=) - coding-synonymous -
./. - c.1578C>T 1578 r.(?) p.(=) - coding-synonymous -
./. - c.1578C>T 1578 r.(?) p.(=) - coding-synonymous -
./. - c.1761G>T 1761 r.(?) p.(=) - coding-synonymous -
./. - c.1761G>T 1761 r.(?) p.(=) - coding-synonymous -
./. - c.1761G>T 1761 r.(?) p.(=) - coding-synonymous -
./. - c.1761G>T 1761 r.(?) p.(=) - coding-synonymous -
./. - c.1761G>T 1761 r.(?) p.(=) - coding-synonymous -
./. - c.1842A>G 1842 r.(?) p.(=) - coding-synonymous -
./. - c.1842A>G 1842 r.(?) p.(=) - coding-synonymous -
./. - c.1842A>G 1842 r.(?) p.(=) - coding-synonymous -
./. - c.1842A>G 1842 r.(?) p.(=) - coding-synonymous -
./. - c.1842A>G 1842 r.(?) p.(=) - coding-synonymous -
./. - c.1842A>G 1842 r.(?) p.(=) - coding-synonymous -
./. - c.1842A>G 1842 r.(?) p.(=) - coding-synonymous -
./. - c.1842A>G 1842 r.(?) p.(=) - coding-synonymous -
./. - c.1842A>G 1842 r.(?) p.(=) - coding-synonymous -
./. - c.1842A>G 1842 r.(?) p.(=) - coding-synonymous -
./. - c.2094A>G 2094 r.(?) p.(=) - coding-synonymous -
./. - c.2094A>G 2094 r.(?) p.(=) - coding-synonymous -
./. - c.2094A>G 2094 r.(?) p.(=) - coding-synonymous -
./. - c.2094A>G 2094 r.(?) p.(=) - coding-synonymous -
./. - c.2658+30T>A 2658 r.(=) p.(=) - intron 30
./. - c.2659-31_2659-28del 2659 r.(=) p.(=) - intron 28
./. - c.2659-31_2659-28del 2659 r.(=) p.(=) - intron 28
./. - c.2659-31_2659-28del 2659 r.(=) p.(=) - intron 28
./. - c.2659-31_2659-28del 2659 r.(=) p.(=) - intron 28
./. - c.2659-29_2659-25del 2659 r.(=) p.(=) - intron 25
./. - c.2659-29_2659-25del 2659 r.(=) p.(=) - intron 25
./. - c.2660T>C 2660 r.(?) p.(Val887Ala) - missense-near-splice -
./. - c.2660T>C 2660 r.(?) p.(Val887Ala) - missense-near-splice -
./. - c.2660T>C 2660 r.(?) p.(Val887Ala) - missense-near-splice -
./. - c.2660T>C 2660 r.(?) p.(Val887Ala) - missense-near-splice -
./. - c.2660T>C 2660 r.(?) p.(Val887Ala) - missense-near-splice -
./. - c.2660T>C 2660 r.(?) p.(Val887Ala) - missense-near-splice -
./. - c.2660T>C 2660 r.(?) p.(Val887Ala) - missense-near-splice -
./. - c.2660T>C 2660 r.(?) p.(Val887Ala) - missense-near-splice -
./. - c.2660T>C 2660 r.(?) p.(Val887Ala) - missense-near-splice -
./. - c.2660T>C 2660 r.(?) p.(Val887Ala) - missense-near-splice -
./. - c.2660T>C 2660 r.(?) p.(Val887Ala) - missense-near-splice -
./. - c.2660T>C 2660 r.(?) p.(Val887Ala) - missense-near-splice -
./. - c.2765C>T 2765 r.(?) p.(Ser922Leu) - missense -
./. - c.2859+49G>A 2859 r.(=) p.(=) - intron 49
./. - c.2859+49G>A 2859 r.(=) p.(=) - intron 49
./. - c.3047-20C>T 3047 r.(=) p.(=) - intron 20
./. - c.3404-34G>A 3404 r.(=) p.(=) - intron 34
./. - c.3404-34G>A 3404 r.(=) p.(=) - intron 34
./. - c.3404-34G>A 3404 r.(=) p.(=) - intron 34
./. - c.3404-34G>A 3404 r.(=) p.(=) - intron 34
./. - c.3404-34G>A 3404 r.(=) p.(=) - intron 34
./. - c.3404-34G>A 3404 r.(=) p.(=) - intron 34
./. - c.3413C>G 3413 r.(?) p.(Pro1138Arg) - missense -
./. - c.3413C>G 3413 r.(?) p.(Pro1138Arg) - missense -
./. - c.3413C>G 3413 r.(?) p.(Pro1138Arg) - missense -
./. - c.3413C>G 3413 r.(?) p.(Pro1138Arg) - missense -
./. - c.3413C>G 3413 r.(?) p.(Pro1138Arg) - missense -
./. - c.3413C>G 3413 r.(?) p.(Pro1138Arg) - missense -
./. - c.3413C>G 3413 r.(?) p.(Pro1138Arg) - missense -
./. - c.3413C>G 3413 r.(?) p.(Pro1138Arg) - missense -
./. - c.3487-3C>T 3487 r.spl? p.? - splice 3
./. - c.3487-3C>T 3487 r.spl? p.? - splice 3
./. - c.3487-3C>T 3487 r.spl? p.? - splice 3
./. - c.3487-3C>T 3487 r.spl? p.? - splice 3
./. - c.3487-3C>T 3487 r.spl? p.? - splice 3
./. - c.3890A>G 3890 r.(?) p.(Lys1297Arg) - missense -
./. - c.4055C>T 4055 r.(?) p.(Ala1352Val) - missense -
./. - c.4055C>T 4055 r.(?) p.(Ala1352Val) - missense -
./. - c.4055C>T 4055 r.(?) p.(Ala1352Val) - missense -
./. - c.4055C>T 4055 r.(?) p.(Ala1352Val) - missense -
./. - c.4055C>T 4055 r.(?) p.(Ala1352Val) - missense -
./. - c.4055C>T 4055 r.(?) p.(Ala1352Val) - missense -
./. - c.4055C>T 4055 r.(?) p.(Ala1352Val) - missense -
./. - c.4055C>T 4055 r.(?) p.(Ala1352Val) - missense -
./. - c.4055C>T 4055 r.(?) p.(Ala1352Val) - missense -
./. - c.*2645G>A 6998 r.(=) p.(=) - utr-3 -
./. - c.*3266G>A 7619 r.(=) p.(=) - utr-3 -
./. - c.*3266G>A 7619 r.(=) p.(=) - utr-3 -
./. - c.*3266G>A 7619 r.(=) p.(=) - utr-3 -
./. - c.*3266G>A 7619 r.(=) p.(=) - utr-3 -
./. - c.*3354C>T 7707 r.(=) p.(=) - utr-3 -
./. - c.*3486G>A 7839 r.(=) p.(=) - utr-3 -
./. - c.*4847C>T 9200 r.(=) p.(=) - utr-3 -
./. - c.*4847C>T 9200 r.(=) p.(=) - utr-3 -
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