Transcript #00003437 (NM_001127663.1, GSN gene)

Transcript name transcript variant 4
Gene name GSN (gelsolin)
Chromosome 9
Transcript - NCBI ID NM_001127663.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001121135.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2013-10-29 15:24:33 +01:00 (CET)
Date last edited N/A


Variants

133 entries on 2 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.-14+21delA -14 r.(=) p.(=) - intron 21
./. - c.-14+21delA -14 r.(=) p.(=) - intron 21
./. - c.-14+21delA -14 r.(=) p.(=) - intron 21
./. - c.-14+21delA -14 r.(=) p.(=) - intron 21
./. - c.-14+21delA -14 r.(=) p.(=) - intron 21
./. - c.-14+27C>T -14 r.(=) p.(=) - intron 27
./. - c.-14+27C>T -14 r.(=) p.(=) - intron 27
./. - c.-14+27C>T -14 r.(=) p.(=) - intron 27
./. - c.-14+27C>T -14 r.(=) p.(=) - intron 27
./. - c.-14+27C>T -14 r.(=) p.(=) - intron 27
./. - c.-14+27C>T -14 r.(=) p.(=) - intron 27
./. - c.-14+27C>T -14 r.(=) p.(=) - intron 27
./. - c.-14+27C>T -14 r.(=) p.(=) - intron 27
./. - c.-14+27C>T -14 r.(=) p.(=) - intron 27
./. - c.-14+27C>T -14 r.(=) p.(=) - intron 27
./. - c.-14+27C>T -14 r.(=) p.(=) - intron 27
./. - c.-14+27C>T -14 r.(=) p.(=) - intron 27
./. - c.-14+27C>T -14 r.(=) p.(=) - intron 27
./. - c.-14+27C>T -14 r.(=) p.(=) - intron 27
./. - c.-14+27C>T -14 r.(=) p.(=) - intron 27
./. - c.-14+27C>T -14 r.(=) p.(=) - intron 27
./. - c.-14+27C>T -14 r.(=) p.(=) - intron 27
./. - c.-14+27C>T -14 r.(=) p.(=) - intron 27
./. - c.-14+27C>T -14 r.(=) p.(=) - intron 27
./. - c.-14+27C>T -14 r.(=) p.(=) - intron 27
./. - c.-14+27C>T -14 r.(=) p.(=) - intron 27
./. - c.137A>G 137 r.(?) p.(Lys46Arg) - missense -
./. - c.340G>A 340 r.(?) p.(Ala114Thr) - missense -
./. - c.340G>A 340 r.(?) p.(Ala114Thr) - missense -
./. - c.340G>A 340 r.(?) p.(Ala114Thr) - missense -
./. - c.340G>A 340 r.(?) p.(Ala114Thr) - missense -
./. - c.340G>A 340 r.(?) p.(Ala114Thr) - missense -
./. - c.340G>A 340 r.(?) p.(Ala114Thr) - missense -
./. - c.340G>A 340 r.(?) p.(Ala114Thr) - missense -
./. - c.351C>T 351 r.(?) p.(=) - coding-synonymous -
./. - c.646A>G 646 r.(?) p.(Asn216Asp) - missense -
./. - c.771+25T>G 771 r.(=) p.(=) - intron 25
./. - c.771+25T>G 771 r.(=) p.(=) - intron 25
./. - c.771+25T>G 771 r.(=) p.(=) - intron 25
./. - c.1083+43G>C 1083 r.(=) p.(=) - intron 43
./. - c.1083+43G>C 1083 r.(=) p.(=) - intron 43
./. - c.1083+43G>C 1083 r.(=) p.(=) - intron 43
./. - c.1083+43G>C 1083 r.(=) p.(=) - intron 43
./. - c.1333G>A 1333 r.(?) p.(Val445Met) - missense -
./. - c.1368C>T 1368 r.(?) p.(=) - coding-synonymous -
./. - c.1368C>T 1368 r.(?) p.(=) - coding-synonymous -
./. - c.1368C>T 1368 r.(?) p.(=) - coding-synonymous -
./. - c.1368C>T 1368 r.(?) p.(=) - coding-synonymous -
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1525-22T>C 1525 r.(=) p.(=) - intron 22
./. - c.1643C>G 1643 r.(?) p.(Thr548Ser) - missense -
./. - c.1695+46A>G 1695 r.(=) p.(=) - intron 46
./. - c.1695+46A>G 1695 r.(=) p.(=) - intron 46
./. - c.1695+46A>G 1695 r.(=) p.(=) - intron 46
./. - c.1802C>T 1802 r.(?) p.(Thr601Met) - missense -
./. - c.1802C>T 1802 r.(?) p.(Thr601Met) - missense -
./. - c.1802C>T 1802 r.(?) p.(Thr601Met) - missense -
./. - c.1802C>T 1802 r.(?) p.(Thr601Met) - missense -
./. - c.1871-34G>A 1871 r.(=) p.(=) - intron 34
./. - c.1871-34G>A 1871 r.(=) p.(=) - intron 34
./. - c.1871-34G>A 1871 r.(=) p.(=) - intron 34
./. - c.1871-34G>A 1871 r.(=) p.(=) - intron 34
./. - c.1871-34G>A 1871 r.(=) p.(=) - intron 34
./. - c.1871-34G>A 1871 r.(=) p.(=) - intron 34
./. - c.1871-34G>A 1871 r.(=) p.(=) - intron 34
./. - c.1871-34G>A 1871 r.(=) p.(=) - intron 34
./. - c.1871-34G>A 1871 r.(=) p.(=) - intron 34
./. - c.1871-34G>A 1871 r.(=) p.(=) - intron 34
./. - c.1871-34G>A 1871 r.(=) p.(=) - intron 34
./. - c.1871-34G>A 1871 r.(=) p.(=) - intron 34
./. - c.1871-34G>A 1871 r.(=) p.(=) - intron 34
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