Transcript #00009269 (NM_001142415.1, AIMP1 gene)

Transcript name transcript variant 2
Gene name AIMP1 (aminoacyl tRNA synthetase complex-interacting multifunctional protein 1)
Chromosome 4
Transcript - NCBI ID NM_001142415.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001135887.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2014-01-21 10:29:25 +01:00 (CET)
Date last edited N/A


Variants

40 entries on 1 page. Showing entries 1 - 40.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.-26+896G>C -26 r.(=) p.(=) - intron 896
./. - c.-26+896G>C -26 r.(=) p.(=) - intron 896
./. - c.-26+896G>C -26 r.(=) p.(=) - intron 896
./. - c.-25-6C>A -25 r.(=) p.(=) - splice 6
./. - c.-25-6C>A -25 r.(=) p.(=) - splice 6
./. - c.-25-6C>A -25 r.(=) p.(=) - splice 6
./. - c.-25-6C>A -25 r.(=) p.(=) - splice 6
./. - c.-25-6C>A -25 r.(=) p.(=) - splice 6
./. - c.-25-6C>A -25 r.(=) p.(=) - splice 6
./. - c.-25-6C>A -25 r.(=) p.(=) - splice 6
./. - c.24G>C 24 r.(?) p.(=) - coding-synonymous -
./. - c.24G>C 24 r.(?) p.(=) - coding-synonymous -
./. - c.24G>C 24 r.(?) p.(=) - coding-synonymous -
./. - c.235C>G 235 r.(?) p.(Pro79Ala) - missense -
./. - c.235C>G 235 r.(?) p.(Pro79Ala) - missense -
./. - c.235C>G 235 r.(?) p.(Pro79Ala) - missense -
./. - c.235C>G 235 r.(?) p.(Pro79Ala) - missense -
./. - c.235C>G 235 r.(?) p.(Pro79Ala) - missense -
./. - c.235C>G 235 r.(?) p.(Pro79Ala) - missense -
./. - c.349A>G 349 r.(?) p.(Thr117Ala) - missense -
./. - c.603+23C>T 603 r.(=) p.(=) - intron 23
./. - c.603+23C>T 603 r.(=) p.(=) - intron 23
./. - c.603+23C>T 603 r.(=) p.(=) - intron 23
./. - c.603+23C>T 603 r.(=) p.(=) - intron 23
./. - c.603+23C>T 603 r.(=) p.(=) - intron 23
./. - c.603+23C>T 603 r.(=) p.(=) - intron 23
./. - c.772+33C>T 772 r.(=) p.(=) - intron 33
./. - c.772+33C>T 772 r.(=) p.(=) - intron 33
./. - c.772+33C>T 772 r.(=) p.(=) - intron 33
./. - c.772+33C>T 772 r.(=) p.(=) - intron 33
./. - c.772+33C>T 772 r.(=) p.(=) - intron 33
./. - c.772+33C>T 772 r.(=) p.(=) - intron 33
./. - c.772+33C>T 772 r.(=) p.(=) - intron 33
./. - c.772+34G>A 772 r.(=) p.(=) - intron 34
./. - c.772+34G>A 772 r.(=) p.(=) - intron 34
./. - c.772+34G>A 772 r.(=) p.(=) - intron 34
./. - c.772+34G>A 772 r.(=) p.(=) - intron 34
./. - c.772+34G>A 772 r.(=) p.(=) - intron 34
./. - c.772+34G>A 772 r.(=) p.(=) - intron 34
./. - c.772+34G>A 772 r.(=) p.(=) - intron 34
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