Transcript #00005855 (NM_000296.3, PKD1 gene)

Transcript name transcript variant 2
Gene name PKD1 (polycystic kidney disease 1 (autosomal dominant))
Chromosome 16
Transcript - NCBI ID NM_000296.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000287.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2013-10-30 10:11:22 +01:00 (CET)
Date last edited N/A


Variants

566 entries on 6 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.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.38T>A 38 r.(?) p.(Leu13Gln) - missense -
./. - c.1607-27C>T 1607 r.(=) p.(=) - intron 27
./. - c.1714C>T 1714 r.(?) p.(Pro572Ser) - missense -
./. - c.1714C>T 1714 r.(?) p.(Pro572Ser) - missense -
./. - c.1849+28_1849+34del 1849 r.(=) p.(=) - intron 28
./. - c.1850-4A>G 1850 r.spl? p.? - splice 4
./. - c.1850-4A>G 1850 r.spl? p.? - splice 4
./. - c.1850-4A>G 1850 r.spl? p.? - splice 4
./. - c.1850-4A>G 1850 r.spl? p.? - splice 4
./. - c.1850-4A>G 1850 r.spl? p.? - splice 4
./. - c.1850-4A>G 1850 r.spl? p.? - splice 4
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2216G>A 2216 r.(?) p.(Arg739Gln) - missense -
./. - c.2700G>A 2700 r.(?) p.(=) - coding-synonymous -
./. - c.2700G>A 2700 r.(?) p.(=) - coding-synonymous -
./. - c.2730C>T 2730 r.(?) p.(=) - coding-synonymous -
./. - c.2730C>T 2730 r.(?) p.(=) - coding-synonymous -
./. - c.2730C>T 2730 r.(?) p.(=) - coding-synonymous -
./. - c.2813C>T 2813 r.(?) p.(Thr938Met) - missense -
./. - c.2813C>T 2813 r.(?) p.(Thr938Met) - missense -
./. - c.2853+23C>T 2853 r.(=) p.(=) - intron 23
./. - c.2854-5C>T 2854 r.spl? p.? - splice 5
./. - c.2854-5C>T 2854 r.spl? p.? - splice 5
./. - c.2986-15C>T 2986 r.(=) p.(=) - intron 15
./. - c.2986-15C>T 2986 r.(=) p.(=) - intron 15
./. - c.2986-15C>T 2986 r.(=) p.(=) - intron 15
./. - c.2986-15C>T 2986 r.(=) p.(=) - intron 15
./. - c.2986-15C>T 2986 r.(=) p.(=) - intron 15
./. - c.3063T>C 3063 r.(?) p.(=) - coding-synonymous -
./. - c.3063T>C 3063 r.(?) p.(=) - coding-synonymous -
./. - c.3063T>C 3063 r.(?) p.(=) - coding-synonymous -
./. - c.3063T>C 3063 r.(?) p.(=) - coding-synonymous -
./. - c.3063T>C 3063 r.(?) p.(=) - coding-synonymous -
./. - c.3063T>C 3063 r.(?) p.(=) - coding-synonymous -
./. - c.3063T>C 3063 r.(?) p.(=) - coding-synonymous -
./. - c.3063T>C 3063 r.(?) p.(=) - coding-synonymous -
./. - c.3063T>C 3063 r.(?) p.(=) - coding-synonymous -
./. - c.3063T>C 3063 r.(?) p.(=) - coding-synonymous -
./. - c.3111A>G 3111 r.(?) p.(=) - coding-synonymous -
./. - c.3275T>C 3275 r.(?) p.(Met1092Thr) - missense -
./. - c.3275T>C 3275 r.(?) p.(Met1092Thr) - missense -
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