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 BAA02g40120 A02 33905380 G A upstream_gene_variant MODIFIER c.-4610G>A| S30
S31
2 BAA02g40120 A02 33905394 C T upstream_gene_variant MODIFIER c.-4596C>T| S105
S106
3 BAA02g40120 A02 33905511 G A upstream_gene_variant MODIFIER c.-4479G>A| S159
4 BAA02g40120 A02 33906464 C T upstream_gene_variant MODIFIER c.-3526C>T| S133
5 BAA02g40120 A02 33906707 G A upstream_gene_variant MODIFIER c.-3283G>A| S8
6 BAA02g40120 A02 33906910 C T upstream_gene_variant MODIFIER c.-3080C>T| S193
7 BAA02g40120 A02 33906938 C T upstream_gene_variant MODIFIER c.-3052C>T| S255
8 BAA02g40120 A02 33907219 C T upstream_gene_variant MODIFIER c.-2771C>T| S3
9 BAA02g40120 A02 33908299 G A upstream_gene_variant MODIFIER c.-1691G>A| S265
10 BAA02g40120 A02 33908690 G A upstream_gene_variant MODIFIER c.-1300G>A| S292
11 BAA02g40120 A02 33909092 C T upstream_gene_variant MODIFIER c.-898C>T| S249
12 BAA02g40120 A02 33909548 C T upstream_gene_variant MODIFIER c.-442C>T| S171
13 BAA02g40120 A02 33910069 C T missense_variant MODERATE c.80C>T|p.Ser27Phe S23
S77
14 BAA02g40120 A02 33910275 C T missense_variant MODERATE c.286C>T|p.Leu96Phe S53
15 BAA02g40120 A02 33910460 C T synonymous_variant LOW c.471C>T|p.Phe157Phe S234
16 BAA02g40120 A02 33910893 C T missense_variant MODERATE c.904C>T|p.His302Tyr S180