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 BAA02g47650 A02 38382492 G A upstream_gene_variant MODIFIER c.-4778G>A| S36
2 BAA02g47650 A02 38383296 G A upstream_gene_variant MODIFIER c.-3974G>A| S276
3 BAA02g47650 A02 38384875 C T upstream_gene_variant MODIFIER c.-2395C>T| S42
4 BAA02g47650 A02 38384982 C T upstream_gene_variant MODIFIER c.-2288C>T| S64
5 BAA02g47650 A02 38384991 G A upstream_gene_variant MODIFIER c.-2279G>A| S242
6 BAA02g47650 A02 38385914 G A upstream_gene_variant MODIFIER c.-1356G>A| S134
7 BAA02g47650 A02 38387298 C T missense_variant MODERATE c.29C>T|p.Ala10Val S32
8 BAA02g47650 A02 38387320 G A stop_gained HIGH c.51G>A|p.Trp17* S19
9 BAA02g47650 A02 38388125 C T synonymous_variant LOW c.636C>T|p.Val212Val S181
10 BAA02g47650 A02 38388842 C T downstream_gene_variant MODIFIER c.*237C>T| S79
S84
11 BAA02g47650 A02 38392967 C T downstream_gene_variant MODIFIER c.*4362C>T| S301
S304
12 BAA02g47650 A02 38393034 G A downstream_gene_variant MODIFIER c.*4429G>A| S30
13 BAA02g47650 A02 38393173 C T downstream_gene_variant MODIFIER c.*4568C>T| S133
14 BAA02g47650 A02 38393558 C T downstream_gene_variant MODIFIER c.*4953C>T| S249