Transcript #00000001 (NM_001198820.1, A1CF gene)

Transcript name transcript variant 6
Gene name A1CF (APOBEC1 complementation factor)
Chromosome 10
Transcript - NCBI ID NM_001198820.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001185749.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2013-10-28 16:39:22 +01:00 (CET)
Date last edited N/A


Variants

59 entries on 1 page. Showing entries 1 - 59.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.132A>G 132 r.(?) p.(=) - coding-synonymous -
./. - c.252T>C 252 r.(?) p.(=) - coding-synonymous -
./. - c.486G>A 486 r.(?) p.(=) - coding-synonymous -
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.892-29C>T 892 r.(=) p.(=) - intron 29
./. - c.1166-48T>C 1166 r.(=) p.(=) - intron 48
./. - c.1266C>T 1266 r.(?) p.(=) - coding-synonymous -
./. - c.1266C>T 1266 r.(?) p.(=) - coding-synonymous -
./. - c.1266C>T 1266 r.(?) p.(=) - coding-synonymous -
./. - c.1266C>T 1266 r.(?) p.(=) - coding-synonymous -
./. - c.1633+17C>T 1633 r.(=) p.(=) - intron 17
./. - c.1633+17C>T 1633 r.(=) p.(=) - intron 17
./. - c.1633+17C>T 1633 r.(=) p.(=) - intron 17
./. - c.1633+17C>T 1633 r.(=) p.(=) - intron 17
./. - c.1633+17C>T 1633 r.(=) p.(=) - intron 17
./. - c.1633+17C>T 1633 r.(=) p.(=) - intron 17
./. - c.1633+17C>T 1633 r.(=) p.(=) - intron 17
./. - c.1633+17C>T 1633 r.(=) p.(=) - intron 17
./. - c.1633+17C>T 1633 r.(=) p.(=) - intron 17
./. - c.1633+17C>T 1633 r.(=) p.(=) - intron 17
./. - c.1633+17C>T 1633 r.(=) p.(=) - intron 17
./. - c.1633+17C>T 1633 r.(=) p.(=) - intron 17
./. - c.1663G>A 1663 r.(?) p.(Val555Met) - missense -
./. - c.1663G>A 1663 r.(?) p.(Val555Met) - missense -
./. - c.1663G>A 1663 r.(?) p.(Val555Met) - missense -
./. - c.1671A>C 1671 r.(?) p.(=) - coding-synonymous -
./. - c.1680C>G 1680 r.(?) p.(=) - coding-synonymous -
./. - c.1680C>G 1680 r.(?) p.(=) - coding-synonymous -
./. - c.1680C>G 1680 r.(?) p.(=) - coding-synonymous -
./. - c.1680C>G 1680 r.(?) p.(=) - coding-synonymous -
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