Transcript #00015445 (NM_001198818.1, A1CF gene)

Transcript name Manually created transcript. (removed from reference sequence)
Gene name A1CF (APOBEC1 complementation factor)
Chromosome 10
Transcript - NCBI ID NM_001198818.1
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.
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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.1142-48T>C 1142 r.(=) p.(=) - intron 48
./. - c.1242C>T 1242 r.(?) p.(=) - coding-synonymous -
./. - c.1242C>T 1242 r.(?) p.(=) - coding-synonymous -
./. - c.1242C>T 1242 r.(?) p.(=) - coding-synonymous -
./. - c.1242C>T 1242 r.(?) p.(=) - coding-synonymous -
./. - c.1609+17C>T 1609 r.(=) p.(=) - intron 17
./. - c.1609+17C>T 1609 r.(=) p.(=) - intron 17
./. - c.1609+17C>T 1609 r.(=) p.(=) - intron 17
./. - c.1609+17C>T 1609 r.(=) p.(=) - intron 17
./. - c.1609+17C>T 1609 r.(=) p.(=) - intron 17
./. - c.1609+17C>T 1609 r.(=) p.(=) - intron 17
./. - c.1609+17C>T 1609 r.(=) p.(=) - intron 17
./. - c.1609+17C>T 1609 r.(=) p.(=) - intron 17
./. - c.1609+17C>T 1609 r.(=) p.(=) - intron 17
./. - c.1609+17C>T 1609 r.(=) p.(=) - intron 17
./. - c.1609+17C>T 1609 r.(=) p.(=) - intron 17
./. - c.1609+17C>T 1609 r.(=) p.(=) - intron 17
./. - c.1639G>A 1639 r.(?) p.(Val547Met) - missense -
./. - c.1639G>A 1639 r.(?) p.(Val547Met) - missense -
./. - c.1639G>A 1639 r.(?) p.(Val547Met) - missense -
./. - c.1647A>C 1647 r.(?) p.(=) - coding-synonymous -
./. - c.1656C>G 1656 r.(?) p.(=) - coding-synonymous -
./. - c.1656C>G 1656 r.(?) p.(=) - coding-synonymous -
./. - c.1656C>G 1656 r.(?) p.(=) - coding-synonymous -
./. - c.1656C>G 1656 r.(?) p.(=) - coding-synonymous -
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