Transcript #00015446 (NM_001198819.1, A1CF gene)

Transcript name Manually created transcript. (removed from reference sequence)
Gene name A1CF (APOBEC1 complementation factor)
Chromosome 10
Transcript - NCBI ID NM_001198819.1
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.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.1166-24T>C 1166 r.(=) p.(=) - intron 24
./. - c.1290C>T 1290 r.(?) p.(=) - coding-synonymous -
./. - c.1290C>T 1290 r.(?) p.(=) - coding-synonymous -
./. - c.1290C>T 1290 r.(?) p.(=) - coding-synonymous -
./. - c.1290C>T 1290 r.(?) p.(=) - coding-synonymous -
./. - c.1657+17C>T 1657 r.(=) p.(=) - intron 17
./. - c.1657+17C>T 1657 r.(=) p.(=) - intron 17
./. - c.1657+17C>T 1657 r.(=) p.(=) - intron 17
./. - c.1657+17C>T 1657 r.(=) p.(=) - intron 17
./. - c.1657+17C>T 1657 r.(=) p.(=) - intron 17
./. - c.1657+17C>T 1657 r.(=) p.(=) - intron 17
./. - c.1657+17C>T 1657 r.(=) p.(=) - intron 17
./. - c.1657+17C>T 1657 r.(=) p.(=) - intron 17
./. - c.1657+17C>T 1657 r.(=) p.(=) - intron 17
./. - c.1657+17C>T 1657 r.(=) p.(=) - intron 17
./. - c.1657+17C>T 1657 r.(=) p.(=) - intron 17
./. - c.1657+17C>T 1657 r.(=) p.(=) - intron 17
./. - c.1687G>A 1687 r.(?) p.(Val563Met) - missense -
./. - c.1687G>A 1687 r.(?) p.(Val563Met) - missense -
./. - c.1687G>A 1687 r.(?) p.(Val563Met) - missense -
./. - c.1695A>C 1695 r.(?) p.(=) - coding-synonymous -
./. - c.1704C>G 1704 r.(?) p.(=) - coding-synonymous -
./. - c.1704C>G 1704 r.(?) p.(=) - coding-synonymous -
./. - c.1704C>G 1704 r.(?) p.(=) - coding-synonymous -
./. - c.1704C>G 1704 r.(?) p.(=) - coding-synonymous -
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