Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 16 of 16 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g15800 A02 7660699 C T synonymous_variant LOW c.102C>T|p.Val34Val S244
2 BAA02g15800 A02 7661607 C T intron_variant MODIFIER c.573+242C>T| S117
3 BAA02g15800 A02 7661803 C T intron_variant MODIFIER c.574-361C>T| S224
4 BAA02g15800 A02 7661813 C T intron_variant MODIFIER c.574-351C>T| S267
5 BAA02g15800 A02 7661928 G A intron_variant MODIFIER c.574-236G>A| S289
S290
6 BAA02g15800 A02 7662253 G A synonymous_variant LOW c.663G>A|p.Lys221Lys S19
7 BAA02g15800 A02 7662716 C T downstream_gene_variant MODIFIER c.*199C>T| S262
8 BAA02g15800 A02 7662997 G A downstream_gene_variant MODIFIER c.*480G>A| S184
9 BAA02g15800 A02 7663016 A T downstream_gene_variant MODIFIER c.*499A>T| S155
10 BAA02g15800 A02 7663834 C T downstream_gene_variant MODIFIER c.*1317C>T| S79
S84
11 BAA02g15800 A02 7664499 C T downstream_gene_variant MODIFIER c.*1982C>T| S13
12 BAA02g15800 A02 7664552 G A downstream_gene_variant MODIFIER c.*2035G>A| S146
13 BAA02g15800 A02 7665121 G A downstream_gene_variant MODIFIER c.*2604G>A| S20
14 BAA02g15800 A02 7665562 C T downstream_gene_variant MODIFIER c.*3045C>T| S144
15 BAA02g15800 A02 7666502 G A downstream_gene_variant MODIFIER c.*3985G>A| S149
16 BAA02g15800 A02 7666505 C T downstream_gene_variant MODIFIER c.*3988C>T| S299