Transcript #00004118 (NM_004523.3, KIF11 gene)

Transcript name kinesin family member 11
Gene name KIF11 (kinesin family member 11)
Chromosome 10
Transcript - NCBI ID NM_004523.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_004514.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2013-10-29 16:37:12 +01:00 (CET)
Date last edited N/A


Variants

48 entries on 1 page. Showing entries 1 - 48.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.309-18A>G 309 r.(=) p.(=) - intron 18
./. - c.309-18A>G 309 r.(=) p.(=) - intron 18
./. - c.309-18A>G 309 r.(=) p.(=) - intron 18
./. - c.309-18A>G 309 r.(=) p.(=) - intron 18
./. - c.309-18A>G 309 r.(=) p.(=) - intron 18
./. - c.309-18A>G 309 r.(=) p.(=) - intron 18
./. - c.309-18A>G 309 r.(=) p.(=) - intron 18
./. - c.309-18A>G 309 r.(=) p.(=) - intron 18
./. - c.387+39A>G 387 r.(=) p.(=) - intron 39
./. - c.387+39A>G 387 r.(=) p.(=) - intron 39
./. - c.387+39A>G 387 r.(=) p.(=) - intron 39
./. - c.387+39A>G 387 r.(=) p.(=) - intron 39
./. - c.387+39A>G 387 r.(=) p.(=) - intron 39
./. - c.387+39A>G 387 r.(=) p.(=) - intron 39
./. - c.387+39A>G 387 r.(=) p.(=) - intron 39
./. - c.574-43G>T 574 r.(=) p.(=) - intron 43
./. - c.574-43G>T 574 r.(=) p.(=) - intron 43
./. - c.1033-37A>G 1033 r.(=) p.(=) - intron 37
./. - c.1033-37A>G 1033 r.(=) p.(=) - intron 37
./. - c.1128+33_1128+35del 1128 r.(=) p.(=) - intron 33
./. - c.1128+33_1128+35del 1128 r.(=) p.(=) - intron 33
./. - c.1128+33_1128+35del 1128 r.(=) p.(=) - intron 33
./. - c.1128+33_1128+35del 1128 r.(=) p.(=) - intron 33
./. - c.1128+33_1128+35del 1128 r.(=) p.(=) - intron 33
./. - c.1128+33_1128+35del 1128 r.(=) p.(=) - intron 33
./. - c.1128+33_1128+35del 1128 r.(=) p.(=) - intron 33
./. - c.1128+33_1128+35del 1128 r.(=) p.(=) - intron 33
./. - c.1129-49T>C 1129 r.(=) p.(=) - intron 49
./. - c.1494+38G>C 1494 r.(=) p.(=) - intron 38
./. - c.1702+9A>T 1702 r.(=) p.(=) - intron 9
./. - c.1702+9A>T 1702 r.(=) p.(=) - intron 9
./. - c.1702+9A>T 1702 r.(=) p.(=) - intron 9
./. - c.1702+9A>T 1702 r.(=) p.(=) - intron 9
./. - c.1702+9A>T 1702 r.(=) p.(=) - intron 9
./. - c.1702+9A>T 1702 r.(=) p.(=) - intron 9
./. - c.1702+9A>T 1702 r.(=) p.(=) - intron 9
./. - c.1706A>G 1706 r.(?) p.(Asn569Ser) - missense -
./. - c.1806G>A 1806 r.(?) p.(=) - coding-synonymous -
./. - c.1876-22A>G 1876 r.(=) p.(=) - intron 22
./. - c.2044C>G 2044 r.(?) p.(Leu682Val) - missense -
./. - c.2770+16A>G 2770 r.(=) p.(=) - intron 16
./. - c.2770+16A>G 2770 r.(=) p.(=) - intron 16
./. - c.2770+16A>G 2770 r.(=) p.(=) - intron 16
./. - c.2922+6T>C 2922 r.(=) p.(=) - splice 6
./. - c.2922+6T>C 2922 r.(=) p.(=) - splice 6
./. - c.2922+6T>C 2922 r.(=) p.(=) - splice 6
./. - c.3040-42G>A 3040 r.(=) p.(=) - intron 42
./. - c.3126G>C 3126 r.(?) p.(Leu1042Phe) - missense -
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