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 BAA02g19090 A02 9892787 C T upstream_gene_variant MODIFIER c.-2453C>T| S284
2 BAA02g19090 A02 9892854 C T upstream_gene_variant MODIFIER c.-2386C>T| S302
3 BAA02g19090 A02 9892937 G A upstream_gene_variant MODIFIER c.-2303G>A| S74
4 BAA02g19090 A02 9893863 G A upstream_gene_variant MODIFIER c.-1377G>A| S62
5 BAA02g19090 A02 9894028 G A upstream_gene_variant MODIFIER c.-1212G>A| S279
6 BAA02g19090 A02 9894249 G A upstream_gene_variant MODIFIER c.-991G>A| S204
7 BAA02g19090 A02 9894279 C T upstream_gene_variant MODIFIER c.-961C>T| S211
S227
8 BAA02g19090 A02 9894298 G A upstream_gene_variant MODIFIER c.-942G>A| S126
9 BAA02g19090 A02 9894352 G A upstream_gene_variant MODIFIER c.-888G>A| S143
10 BAA02g19090 A02 9894381 G A upstream_gene_variant MODIFIER c.-859G>A| S170
11 BAA02g19090 A02 9895486 C T missense_variant MODERATE c.247C>T|p.Arg83Cys S170
12 BAA02g19090 A02 9895630 G A missense_variant MODERATE c.391G>A|p.Val131Ile S149
13 BAA02g19090 A02 9896586 C T missense_variant MODERATE c.707C>T|p.Pro236Leu S249
14 BAA02g19090 A02 9896746 G A synonymous_variant LOW c.867G>A|p.Leu289Leu S272