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 BAA10g05030 A10 2559223 G A upstream_gene_variant MODIFIER c.-3322G>A| S302
2 BAA10g05030 A10 2559523 G A upstream_gene_variant MODIFIER c.-3022G>A| S38
3 BAA10g05030 A10 2559729 G A upstream_gene_variant MODIFIER c.-2816G>A| S148
S210
S30
S31
4 BAA10g05030 A10 2559912 G A upstream_gene_variant MODIFIER c.-2633G>A| S72
S78
5 BAA10g05030 A10 2560011 G A upstream_gene_variant MODIFIER c.-2534G>A| S1
S90
6 BAA10g05030 A10 2560375 C T upstream_gene_variant MODIFIER c.-2170C>T| S298
7 BAA10g05030 A10 2560430 C T upstream_gene_variant MODIFIER c.-2115C>T| S149
8 BAA10g05030 A10 2561350 G A upstream_gene_variant MODIFIER c.-1195G>A| S208
S219
9 BAA10g05030 A10 2561834 C T upstream_gene_variant MODIFIER c.-711C>T| S23
10 BAA10g05030 A10 2561935 C T upstream_gene_variant MODIFIER c.-610C>T| S142
11 BAA10g05030 A10 2563559 G A downstream_gene_variant MODIFIER c.*763G>A| S69
12 BAA10g05030 A10 2563570 G A downstream_gene_variant MODIFIER c.*774G>A| S198
13 BAA10g05030 A10 2565902 G A downstream_gene_variant MODIFIER c.*3106G>A| S289
14 BAA10g05030 A10 2566063 C T downstream_gene_variant MODIFIER c.*3267C>T| S2