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


Gene ID

Results: 1 - 18 of 18 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g29020 A02 16500742 G A upstream_gene_variant MODIFIER c.-4971G>A| S61
2 BAA02g29020 A02 16500983 G A upstream_gene_variant MODIFIER c.-4730G>A| S155
S211
3 BAA02g29020 A02 16501225 C T upstream_gene_variant MODIFIER c.-4488C>T| S284
4 BAA02g29020 A02 16502809 G A upstream_gene_variant MODIFIER c.-2904G>A| S263
5 BAA02g29020 A02 16502848 G A upstream_gene_variant MODIFIER c.-2865G>A| S200
6 BAA02g29020 A02 16502893 G A upstream_gene_variant MODIFIER c.-2820G>A| S148
S30
S31
7 BAA02g29020 A02 16503338 G A upstream_gene_variant MODIFIER c.-2375G>A| S155
8 BAA02g29020 A02 16504083 C T upstream_gene_variant MODIFIER c.-1630C>T| S296
9 BAA02g29020 A02 16504511 G A upstream_gene_variant MODIFIER c.-1202G>A| S294
10 BAA02g29020 A02 16504613 C T upstream_gene_variant MODIFIER c.-1100C>T| S221
11 BAA02g29020 A02 16505871 G A intron_variant MODIFIER c.119-40G>A| S156
12 BAA02g29020 A02 16506398 C T missense_variant MODERATE c.394C>T|p.Pro132Ser S282
13 BAA02g29020 A02 16508178 G A synonymous_variant LOW c.1221G>A|p.Glu407Glu S17
14 BAA02g29020 A02 16509019 C T synonymous_variant LOW c.1618C>T|p.Leu540Leu S224
15 BAA02g29020 A02 16509132 G A missense_variant MODERATE c.1640G>A|p.Arg547Lys S263
16 BAA02g29020 A02 16509748 G A downstream_gene_variant MODIFIER c.*585G>A| S95
17 BAA02g29020 A02 16509915 C T downstream_gene_variant MODIFIER c.*752C>T| S193
18 BAA02g29020 A02 16510171 C T downstream_gene_variant MODIFIER c.*1008C>T| S135