Transcript #00015448 (NM_138932.2, A1CF gene)

Transcript name Manually created transcript. (removed from reference sequence)
Gene name A1CF (APOBEC1 complementation factor)
Chromosome 10
Transcript - NCBI ID NM_138932.2
Transcript - Ensembl ID -
Protein - NCBI ID -
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

59 entries on 1 page. Showing entries 1 - 59.
Legend   How to query  

Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.108A>G 108 r.(?) p.(=) - coding-synonymous -
./. - c.228T>C 228 r.(?) p.(=) - coding-synonymous -
./. - c.462G>A 462 r.(?) p.(=) - coding-synonymous -
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.868-29C>T 868 r.(=) p.(=) - intron 29
./. - c.1142-24T>C 1142 r.(=) p.(=) - intron 24
./. - 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 -
Legend   How to query