Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 14 of 14 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g07790 A05 3903715 G A upstream_gene_variant MODIFIER c.-4968G>A| S298
2 BAA05g07790 A05 3905618 G A upstream_gene_variant MODIFIER c.-3065G>A| S192
3 BAA05g07790 A05 3905723 G A upstream_gene_variant MODIFIER c.-2960G>A| S192
4 BAA05g07790 A05 3906180 A T upstream_gene_variant MODIFIER c.-2503A>T| S280
5 BAA05g07790 A05 3907945 G A upstream_gene_variant MODIFIER c.-738G>A| S262
6 BAA05g07790 A05 3908801 C T missense_variant MODERATE c.119C>T|p.Ala40Val S167
7 BAA05g07790 A05 3909797 C T intron_variant MODIFIER c.636+479C>T| S107
8 BAA05g07790 A05 3909851 C T intron_variant MODIFIER c.636+533C>T| S36
9 BAA05g07790 A05 3910667 C T synonymous_variant LOW c.751C>T|p.Leu251Leu S153
S213
10 BAA05g07790 A05 3911018 G A missense_variant MODERATE c.1102G>A|p.Glu368Lys S294
11 BAA05g07790 A05 3911057 T C missense_variant MODERATE c.1141T>C|p.Cys381Arg S97
12 BAA05g07790 A05 3911310 G A missense_variant MODERATE c.1394G>A|p.Arg465Lys S109
13 BAA05g07790 A05 3911552 C T downstream_gene_variant MODIFIER c.*130C>T| S10
14 BAA05g07790 A05 3911664 T C downstream_gene_variant MODIFIER c.*242T>C| S187