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 BAA01g24450 A01 12950866 G A upstream_gene_variant MODIFIER c.-2256G>A| S197
2 BAA01g24450 A01 12951045 C T upstream_gene_variant MODIFIER c.-2077C>T| S153
3 BAA01g24450 A01 12952402 G A upstream_gene_variant MODIFIER c.-720G>A| S74
4 BAA01g24450 A01 12953434 C T intron_variant MODIFIER c.27+286C>T| S89
5 BAA01g24450 A01 12955934 G A downstream_gene_variant MODIFIER c.*1266G>A| S37
6 BAA01g24450 A01 12956577 C T downstream_gene_variant MODIFIER c.*1909C>T| S69
7 BAA01g24450 A01 12956622 C T downstream_gene_variant MODIFIER c.*1954C>T| S153
8 BAA01g24450 A01 12956685 C T downstream_gene_variant MODIFIER c.*2017C>T| S171
9 BAA01g24450 A01 12957406 C T downstream_gene_variant MODIFIER c.*2738C>T| S96
10 BAA01g24450 A01 12957526 C T downstream_gene_variant MODIFIER c.*2858C>T| S295
11 BAA01g24450 A01 12957693 C T downstream_gene_variant MODIFIER c.*3025C>T| S208
S93
12 BAA01g24450 A01 12958539 G A downstream_gene_variant MODIFIER c.*3871G>A| S191
13 BAA01g24450 A01 12958963 C T downstream_gene_variant MODIFIER c.*4295C>T| S47
14 BAA01g24450 A01 12959561 C T downstream_gene_variant MODIFIER c.*4893C>T| S177