Transcript #00023143 (NM_001114382.1, TSC2 gene)

Transcript name transcript variant 5
Gene name TSC2 (tuberous sclerosis 2)
Chromosome 16
Transcript - NCBI ID NM_001114382.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001107854.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

215 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.-3443A>G -3443 r.(=) p.(=) - utr-5 -
./. - c.-29-239C>T -29 r.(=) p.(=) - intron 239
./. - c.138+14C>G 138 r.(=) p.(=) - intron 14
./. - c.336+33G>T 336 r.(=) p.(=) - intron 33
./. - c.336+33G>T 336 r.(=) p.(=) - intron 33
./. - c.336+33G>T 336 r.(=) p.(=) - intron 33
./. - c.482-3C>T 482 r.spl? p.? - splice 3
./. - c.482-3C>T 482 r.spl? p.? - splice 3
./. - c.482-3C>T 482 r.spl? p.? - splice 3
./. - c.482-3C>T 482 r.spl? p.? - splice 3
./. - c.482-3C>T 482 r.spl? p.? - splice 3
./. - c.482-3C>T 482 r.spl? p.? - splice 3
./. - c.856A>G 856 r.(?) p.(Met286Val) - missense -
./. - c.856A>G 856 r.(?) p.(Met286Val) - missense -
./. - c.856A>G 856 r.(?) p.(Met286Val) - missense -
./. - c.856A>G 856 r.(?) p.(Met286Val) - missense -
./. - c.856A>G 856 r.(?) p.(Met286Val) - missense -
./. - c.1578C>T 1578 r.(?) p.(=) - coding-synonymous -
./. - c.1600-39C>T 1600 r.(=) p.(=) - intron 39
./. - c.1600-39C>T 1600 r.(=) p.(=) - intron 39
./. - c.1600-14C>T 1600 r.(=) p.(=) - intron 14
./. - c.1865G>A 1865 r.(?) p.(Arg622Gln) - missense -
./. - c.2221-28A>G 2221 r.(=) p.(=) - intron 28
./. - c.2221-28A>G 2221 r.(=) p.(=) - intron 28
./. - c.2221-28A>G 2221 r.(=) p.(=) - intron 28
./. - c.2221-28A>G 2221 r.(=) p.(=) - intron 28
./. - c.2221-28A>G 2221 r.(=) p.(=) - intron 28
./. - c.2221-28A>G 2221 r.(=) p.(=) - intron 28
./. - c.2221-28A>G 2221 r.(=) p.(=) - intron 28
./. - c.2221-28A>G 2221 r.(=) p.(=) - intron 28
./. - c.2356-15T>A 2356 r.(=) p.(=) - intron 15
./. - c.2356-15T>A 2356 r.(=) p.(=) - intron 15
./. - c.2356-15T>A 2356 r.(=) p.(=) - intron 15
./. - c.2546-12C>T 2546 r.(=) p.(=) - intron 12
./. - c.2546-12C>T 2546 r.(=) p.(=) - intron 12
./. - c.2546-12C>T 2546 r.(=) p.(=) - intron 12
./. - c.2546-12C>T 2546 r.(=) p.(=) - intron 12
./. - c.2546-12C>T 2546 r.(=) p.(=) - intron 12
./. - c.2546-12C>T 2546 r.(=) p.(=) - intron 12
./. - c.2546-12C>T 2546 r.(=) p.(=) - intron 12
./. - c.2546-12C>T 2546 r.(=) p.(=) - intron 12
./. - c.2546-12C>T 2546 r.(=) p.(=) - intron 12
./. - c.2546-12C>T 2546 r.(=) p.(=) - intron 12
./. - c.2546-12C>T 2546 r.(=) p.(=) - intron 12
./. - c.2546-12C>T 2546 r.(=) p.(=) - intron 12
./. - c.2546-12C>T 2546 r.(=) p.(=) - intron 12
./. - c.2546-12C>T 2546 r.(=) p.(=) - intron 12
./. - c.2580T>C 2580 r.(?) p.(=) - coding-synonymous -
./. - c.2580T>C 2580 r.(?) p.(=) - coding-synonymous -
./. - c.2639+44C>G 2639 r.(=) p.(=) - intron 44
./. - c.2639+44C>G 2639 r.(=) p.(=) - intron 44
./. - c.2639+44C>G 2639 r.(=) p.(=) - intron 44
./. - c.2639+44C>G 2639 r.(=) p.(=) - intron 44
./. - c.2639+44C>G 2639 r.(=) p.(=) - intron 44
./. - c.2639+44C>G 2639 r.(=) p.(=) - intron 44
./. - c.2639+44C>G 2639 r.(=) p.(=) - intron 44
./. - c.2639+44C>G 2639 r.(=) p.(=) - intron 44
./. - c.2639+44C>G 2639 r.(=) p.(=) - intron 44
./. - c.2870T>G 2870 r.(?) p.(Leu957Trp) - missense -
./. - c.3126G>C 3126 r.(?) p.(=) - coding-synonymous -
./. - c.3126G>C 3126 r.(?) p.(=) - coding-synonymous -
./. - c.3126G>C 3126 r.(?) p.(=) - coding-synonymous -
./. - c.3199G>C 3199 r.(?) p.(Val1067Leu) - missense -
./. - c.3610+34C>T 3610 r.(=) p.(=) - intron 34
./. - c.3610+41_3610+42insC 3610 r.(=) p.(=) - intron 41
./. - c.3610+41_3610+42insC 3610 r.(=) p.(=) - intron 41
./. - c.3803G>A 3803 r.(?) p.(Arg1268His) - missense -
./. - c.3845C>T 3845 r.(?) p.(Pro1282Leu) - missense -
./. - c.3846G>A 3846 r.(?) p.(=) - coding-synonymous -
./. - c.3846G>A 3846 r.(?) p.(=) - coding-synonymous -
./. - c.3917G>A 3917 r.(?) p.(Arg1306His) - missense -
./. - c.4216G>T 4216 r.(?) p.(Ala1406Ser) - missense -
./. - c.4424+18G>A 4424 r.(=) p.(=) - intron 18
./. - c.4500+47G>A 4500 r.(=) p.(=) - intron 47
./. - c.4914C>T 4914 r.(?) p.(=) - coding-synonymous -
./. - c.4956G>A 4956 r.(?) p.(=) - coding-synonymous -
./. - c.5092-10A>C 5092 r.(=) p.(=) - intron 10
./. - c.5092-10A>C 5092 r.(=) p.(=) - intron 10
./. - c.5092-10A>C 5092 r.(=) p.(=) - intron 10
./. - c.5092-10A>C 5092 r.(=) p.(=) - intron 10
./. - c.5092-10A>C 5092 r.(=) p.(=) - intron 10
./. - c.5092-10A>C 5092 r.(=) p.(=) - intron 10
./. - c.5092-10A>C 5092 r.(=) p.(=) - intron 10
./. - c.5092-10A>C 5092 r.(=) p.(=) - intron 10
./. - c.5092-10A>C 5092 r.(=) p.(=) - intron 10
./. - c.5092-10A>C 5092 r.(=) p.(=) - intron 10
./. - c.5092-10A>C 5092 r.(=) p.(=) - intron 10
./. - c.5092-10A>C 5092 r.(=) p.(=) - intron 10
./. - c.5092-10A>C 5092 r.(=) p.(=) - intron 10
./. - c.5092-10A>C 5092 r.(=) p.(=) - intron 10
./. - c.5092-10A>C 5092 r.(=) p.(=) - intron 10
./. - c.5092-10A>C 5092 r.(=) p.(=) - intron 10
./. - c.5092-10A>C 5092 r.(=) p.(=) - intron 10
./. - c.5092-10A>C 5092 r.(=) p.(=) - intron 10
./. - c.5133T>C 5133 r.(?) p.(=) - coding-synonymous -
./. - c.5133T>C 5133 r.(?) p.(=) - coding-synonymous -
./. - c.5133T>C 5133 r.(?) p.(=) - coding-synonymous -
./. - c.5133T>C 5133 r.(?) p.(=) - coding-synonymous -
./. - c.5133T>C 5133 r.(?) p.(=) - coding-synonymous -
./. - c.5133T>C 5133 r.(?) p.(=) - coding-synonymous -
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