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 BAA02g13210 A02 5984262 C T upstream_gene_variant MODIFIER c.-3668C>T| S280
2 BAA02g13210 A02 5985231 C T upstream_gene_variant MODIFIER c.-2699C>T| S306
S308
3 BAA02g13210 A02 5985327 C T upstream_gene_variant MODIFIER c.-2603C>T| S267
4 BAA02g13210 A02 5986650 G A upstream_gene_variant MODIFIER c.-1280G>A| S168
5 BAA02g13210 A02 5986719 G A upstream_gene_variant MODIFIER c.-1211G>A| S136
6 BAA02g13210 A02 5988116 C T missense_variant MODERATE c.187C>T|p.Pro63Ser S226
7 BAA02g13210 A02 5988458 C T intron_variant MODIFIER c.394+135C>T| S162
8 BAA02g13210 A02 5990669 C T downstream_gene_variant MODIFIER c.*1684C>T| S289
S290
9 BAA02g13210 A02 5990911 G A downstream_gene_variant MODIFIER c.*1926G>A| S53
10 BAA02g13210 A02 5992173 C T downstream_gene_variant MODIFIER c.*3188C>T| S262
11 BAA02g13210 A02 5992197 A C downstream_gene_variant MODIFIER c.*3212A>C|
12 BAA02g13210 A02 5992237 C T downstream_gene_variant MODIFIER c.*3252C>T| S40
S49
13 BAA02g13210 A02 5992704 C T downstream_gene_variant MODIFIER c.*3719C>T| S273
14 BAA02g13210 A02 5992803 C T downstream_gene_variant MODIFIER c.*3818C>T| S261