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 BAA02g45920 A02 37472329 C T missense_variant MODERATE c.176G>A|p.Arg59Gln S193
2 BAA02g45920 A02 37472764 C T upstream_gene_variant MODIFIER c.-260G>A| S221
3 BAA02g45920 A02 37473571 C T upstream_gene_variant MODIFIER c.-1067G>A| S237
4 BAA02g45920 A02 37473663 C T upstream_gene_variant MODIFIER c.-1159G>A| S295
5 BAA02g45920 A02 37473794 C T upstream_gene_variant MODIFIER c.-1290G>A| S182
6 BAA02g45920 A02 37474466 T A upstream_gene_variant MODIFIER c.-1962A>T| S75
S81
7 BAA02g45920 A02 37474962 C T upstream_gene_variant MODIFIER c.-2458G>A| S189
8 BAA02g45920 A02 37475081 C T upstream_gene_variant MODIFIER c.-2577G>A| S234
9 BAA02g45920 A02 37475588 G A upstream_gene_variant MODIFIER c.-3084C>T| S267
10 BAA02g45920 A02 37475679 C T upstream_gene_variant MODIFIER c.-3175G>A| S87
11 BAA02g45920 A02 37476050 C T upstream_gene_variant MODIFIER c.-3546G>A| S149
12 BAA02g45920 A02 37476077 C T upstream_gene_variant MODIFIER c.-3573G>A| S129
13 BAA02g45920 A02 37476393 G A upstream_gene_variant MODIFIER c.-3889C>T| S280
14 BAA02g45920 A02 37477402 G A upstream_gene_variant MODIFIER c.-4898C>T| S192