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


Gene ID

Results: 1 - 15 of 15 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA05g01130 A05 652601 C T downstream_gene_variant MODIFIER c.*3985G>A| S235
2 BAA05g01130 A05 652949 C T downstream_gene_variant MODIFIER c.*3637G>A| S123
3 BAA05g01130 A05 654001 C T downstream_gene_variant MODIFIER c.*2585G>A| S205
4 BAA05g01130 A05 655557 C T downstream_gene_variant MODIFIER c.*1029G>A| S120
5 BAA05g01130 A05 656561 G A downstream_gene_variant MODIFIER c.*25C>T| S155
S211
6 BAA05g01130 A05 657338 G A splice_region_variant&synonymous_variant LOW c.669C>T|p.Ala223Ala S86
7 BAA05g01130 A05 657643 C T missense_variant MODERATE c.536G>A|p.Gly179Glu S268
8 BAA05g01130 A05 657892 C T intron_variant MODIFIER c.426-139G>A| S2
9 BAA05g01130 A05 659139 C T synonymous_variant LOW c.135G>A|p.Thr45Thr S202
10 BAA05g01130 A05 660250 G A upstream_gene_variant MODIFIER c.-977C>T| S77
S82
11 BAA05g01130 A05 661779 C T upstream_gene_variant MODIFIER c.-2506G>A| S135
12 BAA05g01130 A05 663796 C T upstream_gene_variant MODIFIER c.-4523G>A| S208
13 BAA05g01130 A05 663861 C T upstream_gene_variant MODIFIER c.-4588G>A| S250
14 BAA05g01130 A05 664034 C T upstream_gene_variant MODIFIER c.-4761G>A| S41
15 BAA05g01130 A05 664224 C T upstream_gene_variant MODIFIER c.-4951G>A| S142