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 BAA07g28460 A07 29654235 G A upstream_gene_variant MODIFIER c.-4374G>A| S208
2 BAA07g28460 A07 29654329 C T upstream_gene_variant MODIFIER c.-4280C>T| S5
3 BAA07g28460 A07 29656040 G A upstream_gene_variant MODIFIER c.-2569G>A| S183
S198
4 BAA07g28460 A07 29656049 C T upstream_gene_variant MODIFIER c.-2560C>T| S221
5 BAA07g28460 A07 29656551 C T upstream_gene_variant MODIFIER c.-2058C>T| S126
6 BAA07g28460 A07 29656573 G A upstream_gene_variant MODIFIER c.-2036G>A| S143
7 BAA07g28460 A07 29656773 C T upstream_gene_variant MODIFIER c.-1836C>T| S306
S308
8 BAA07g28460 A07 29656839 C T upstream_gene_variant MODIFIER c.-1770C>T| S58
9 BAA07g28460 A07 29657089 G A upstream_gene_variant MODIFIER c.-1520G>A| S128
10 BAA07g28460 A07 29657355 C T upstream_gene_variant MODIFIER c.-1254C>T| S161
11 BAA07g28460 A07 29657857 G A upstream_gene_variant MODIFIER c.-752G>A| S303
12 BAA07g28460 A07 29658183 C T upstream_gene_variant MODIFIER c.-426C>T| S302
13 BAA07g28460 A07 29661371 G A missense_variant MODERATE c.871G>A|p.Asp291Asn S16
14 BAA07g28460 A07 29662039 C T missense_variant MODERATE c.1267C>T|p.Pro423Ser S181