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 BAA01g21560 A01 10701932 G A upstream_gene_variant MODIFIER c.-4058G>A| S199
2 BAA01g21560 A01 10702207 C T upstream_gene_variant MODIFIER c.-3783C>T| S16
3 BAA01g21560 A01 10702865 G A upstream_gene_variant MODIFIER c.-3125G>A| S75
S81
4 BAA01g21560 A01 10702912 C T upstream_gene_variant MODIFIER c.-3078C>T| S256
5 BAA01g21560 A01 10703009 G A upstream_gene_variant MODIFIER c.-2981G>A| S34
6 BAA01g21560 A01 10703893 C T upstream_gene_variant MODIFIER c.-2097C>T| S305
7 BAA01g21560 A01 10704082 C T upstream_gene_variant MODIFIER c.-1908C>T| S53
8 BAA01g21560 A01 10704109 G A upstream_gene_variant MODIFIER c.-1881G>A| S109
9 BAA01g21560 A01 10704804 C T upstream_gene_variant MODIFIER c.-1186C>T| S166
10 BAA01g21560 A01 10705487 C T upstream_gene_variant MODIFIER c.-503C>T| S100
11 BAA01g21560 A01 10705503 C T upstream_gene_variant MODIFIER c.-487C>T| S150
12 BAA01g21560 A01 10705721 G A upstream_gene_variant MODIFIER c.-269G>A| S275
13 BAA01g21560 A01 10707016 C T downstream_gene_variant MODIFIER c.*694C>T| S286
14 BAA01g21560 A01 10707306 C T downstream_gene_variant MODIFIER c.*984C>T| S111