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 BAA02g34950 A02 30076182 C T upstream_gene_variant MODIFIER c.-4414C>T| S177
2 BAA02g34950 A02 30076432 G A upstream_gene_variant MODIFIER c.-4164G>A| S298
3 BAA02g34950 A02 30077024 C T upstream_gene_variant MODIFIER c.-3572C>T| S193
4 BAA02g34950 A02 30077190 C T upstream_gene_variant MODIFIER c.-3406C>T| S25
S264
5 BAA02g34950 A02 30078381 C T upstream_gene_variant MODIFIER c.-2215C>T| S162
6 BAA02g34950 A02 30078609 C T upstream_gene_variant MODIFIER c.-1987C>T| S171
7 BAA02g34950 A02 30079936 G A upstream_gene_variant MODIFIER c.-660G>A| S110
8 BAA02g34950 A02 30080003 C T upstream_gene_variant MODIFIER c.-593C>T| S164
9 BAA02g34950 A02 30080020 G A upstream_gene_variant MODIFIER c.-576G>A| S245
10 BAA02g34950 A02 30080055 C T upstream_gene_variant MODIFIER c.-541C>T| S260
11 BAA02g34950 A02 30080115 G A upstream_gene_variant MODIFIER c.-481G>A| S186
12 BAA02g34950 A02 30080808 G A synonymous_variant LOW c.213G>A|p.Val71Val S125
13 BAA02g34950 A02 30080946 G A synonymous_variant LOW c.351G>A|p.Gln117Gln S126
14 BAA02g34950 A02 30082252 G A missense_variant MODERATE c.1336G>A|p.Asp446Asn S297
15 BAA02g34950 A02 30083682 C T downstream_gene_variant MODIFIER c.*1081C>T| S116
16 BAA02g34950 A02 30083789 G A downstream_gene_variant MODIFIER c.*1188G>A| S169
17 BAA02g34950 A02 30084061 C T downstream_gene_variant MODIFIER c.*1460C>T| S121