Transcript #00023635 (NM_001135243.1, TCOF1 gene)

Transcript name Manually created transcript
Gene name TCOF1 (Treacher Collins-Franceschetti syndrome 1)
Chromosome 5
Transcript - NCBI ID NM_001135243.1
Transcript - Ensembl ID -
Protein - NCBI ID -
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
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.3518-34G>A 3518 r.(=) p.(=) - intron 34
./. - c.3518-34G>A 3518 r.(=) p.(=) - intron 34
./. - c.3518-34G>A 3518 r.(=) p.(=) - intron 34
./. - c.3518-34G>A 3518 r.(=) p.(=) - intron 34
./. - c.3518-34G>A 3518 r.(=) p.(=) - intron 34
./. - c.3518-34G>A 3518 r.(=) p.(=) - intron 34
./. - c.3527C>G 3527 r.(?) p.(Pro1176Arg) - missense -
./. - c.3527C>G 3527 r.(?) p.(Pro1176Arg) - missense -
./. - c.3527C>G 3527 r.(?) p.(Pro1176Arg) - missense -
./. - c.3527C>G 3527 r.(?) p.(Pro1176Arg) - missense -
./. - c.3527C>G 3527 r.(?) p.(Pro1176Arg) - missense -
./. - c.3527C>G 3527 r.(?) p.(Pro1176Arg) - missense -
./. - c.3527C>G 3527 r.(?) p.(Pro1176Arg) - missense -
./. - c.3527C>G 3527 r.(?) p.(Pro1176Arg) - missense -
./. - c.3601-3C>T 3601 r.spl? p.? - splice 3
./. - c.3601-3C>T 3601 r.spl? p.? - splice 3
./. - c.3601-3C>T 3601 r.spl? p.? - splice 3
./. - c.3601-3C>T 3601 r.spl? p.? - splice 3
./. - c.3601-3C>T 3601 r.spl? p.? - splice 3
./. - c.4004A>G 4004 r.(?) p.(Lys1335Arg) - missense -
./. - c.4169C>T 4169 r.(?) p.(Ala1390Val) - missense -
./. - c.4169C>T 4169 r.(?) p.(Ala1390Val) - missense -
./. - c.4169C>T 4169 r.(?) p.(Ala1390Val) - missense -
./. - c.4169C>T 4169 r.(?) p.(Ala1390Val) - missense -
./. - c.4169C>T 4169 r.(?) p.(Ala1390Val) - missense -
./. - c.4169C>T 4169 r.(?) p.(Ala1390Val) - missense -
./. - c.4169C>T 4169 r.(?) p.(Ala1390Val) - missense -
./. - c.4169C>T 4169 r.(?) p.(Ala1390Val) - missense -
./. - c.4169C>T 4169 r.(?) p.(Ala1390Val) - missense -
./. - c.*2645G>A 7112 r.(=) p.(=) - utr-3 -
./. - c.*3266G>A 7733 r.(=) p.(=) - utr-3 -
./. - c.*3266G>A 7733 r.(=) p.(=) - utr-3 -
./. - c.*3266G>A 7733 r.(=) p.(=) - utr-3 -
./. - c.*3266G>A 7733 r.(=) p.(=) - utr-3 -
./. - c.*3354C>T 7821 r.(=) p.(=) - utr-3 -
./. - c.*3486G>A 7953 r.(=) p.(=) - utr-3 -
./. - c.*4847C>T 9314 r.(=) p.(=) - utr-3 -
./. - c.*4847C>T 9314 r.(=) p.(=) - utr-3 -
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