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


Gene ID

Results: 1 - 17 of 17 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA02g41170 A02 34549649 C T upstream_gene_variant MODIFIER c.-4480C>T| S308
2 BAA02g41170 A02 34551000 G A upstream_gene_variant MODIFIER c.-3129G>A| S188
3 BAA02g41170 A02 34551165 C T upstream_gene_variant MODIFIER c.-2964C>T| S74
4 BAA02g41170 A02 34551291 C T upstream_gene_variant MODIFIER c.-2838C>T| S130
5 BAA02g41170 A02 34551353 C T upstream_gene_variant MODIFIER c.-2776C>T| S3
6 BAA02g41170 A02 34551408 G A upstream_gene_variant MODIFIER c.-2721G>A| S132
S137
S138
S215
S288
S89
7 BAA02g41170 A02 34551864 C T upstream_gene_variant MODIFIER c.-2265C>T| S261
8 BAA02g41170 A02 34552597 C T upstream_gene_variant MODIFIER c.-1532C>T| S64
9 BAA02g41170 A02 34552755 C T upstream_gene_variant MODIFIER c.-1374C>T| S218
10 BAA02g41170 A02 34553370 G A upstream_gene_variant MODIFIER c.-759G>A| S225
11 BAA02g41170 A02 34554166 C T missense_variant MODERATE c.38C>T|p.Ala13Val S54
12 BAA02g41170 A02 34555517 C T synonymous_variant LOW c.739C>T|p.Leu247Leu S295
13 BAA02g41170 A02 34555638 G A missense_variant MODERATE c.860G>A|p.Arg287Lys S279
14 BAA02g41170 A02 34555768 G A synonymous_variant LOW c.990G>A|p.Thr330Thr S256
15 BAA02g41170 A02 34556311 C T downstream_gene_variant MODIFIER c.*327C>T| S12
16 BAA02g41170 A02 34556822 G A downstream_gene_variant MODIFIER c.*838G>A| S69
17 BAA02g41170 A02 34557396 G A downstream_gene_variant MODIFIER c.*1412G>A| S159
S243