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 BAA02g33050 A02 28309440 C T intron_variant MODIFIER c.1076+117G>A| S115
2 BAA02g33050 A02 28310051 C T missense_variant MODERATE c.754G>A|p.Gly252Arg S296
3 BAA02g33050 A02 28310283 G A intron_variant MODIFIER c.631-32C>T| S95
4 BAA02g33050 A02 28310676 G A intron_variant MODIFIER c.483-31C>T| S247
5 BAA02g33050 A02 28312275 G A upstream_gene_variant MODIFIER c.-342C>T| S298
6 BAA02g33050 A02 28312984 C T upstream_gene_variant MODIFIER c.-1051G>A| S180
7 BAA02g33050 A02 28313753 C T upstream_gene_variant MODIFIER c.-1820G>A| S157
S163
8 BAA02g33050 A02 28313768 C T upstream_gene_variant MODIFIER c.-1835G>A| S119
9 BAA02g33050 A02 28313873 C T upstream_gene_variant MODIFIER c.-1940G>A| S201
10 BAA02g33050 A02 28314287 G A upstream_gene_variant MODIFIER c.-2354C>T| S204
11 BAA02g33050 A02 28314837 C T upstream_gene_variant MODIFIER c.-2904G>A| S66
12 BAA02g33050 A02 28315847 C T upstream_gene_variant MODIFIER c.-3914G>A| S202
13 BAA02g33050 A02 28316180 C T upstream_gene_variant MODIFIER c.-4247G>A| S9
14 BAA02g33050 A02 28316891 G A upstream_gene_variant MODIFIER c.-4958C>T| S197