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


Gene ID

Results: 1 - 18 of 18 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA01g15330 A01 7362763 C T upstream_gene_variant MODIFIER c.-1297C>T| S89
2 BAA01g15330 A01 7363034 C T upstream_gene_variant MODIFIER c.-1026C>T| S177
3 BAA01g15330 A01 7363142 C T upstream_gene_variant MODIFIER c.-918C>T| S246
4 BAA01g15330 A01 7363317 G A upstream_gene_variant MODIFIER c.-743G>A| S187
5 BAA01g15330 A01 7363356 C T upstream_gene_variant MODIFIER c.-704C>T| S52
6 BAA01g15330 A01 7363605 C T upstream_gene_variant MODIFIER c.-455C>T| S264
7 BAA01g15330 A01 7363638 C T upstream_gene_variant MODIFIER c.-422C>T| S213
8 BAA01g15330 A01 7364125 C T synonymous_variant LOW c.66C>T|p.Gly22Gly S36
9 BAA01g15330 A01 7364241 C T missense_variant MODERATE c.182C>T|p.Ser61Phe S85
10 BAA01g15330 A01 7364281 G A synonymous_variant LOW c.222G>A|p.Arg74Arg S28
11 BAA01g15330 A01 7364368 C T synonymous_variant LOW c.309C>T|p.Ser103Ser S179
12 BAA01g15330 A01 7364381 G A missense_variant MODERATE c.322G>A|p.Glu108Lys S263
13 BAA01g15330 A01 7364412 C T missense_variant MODERATE c.353C>T|p.Ala118Val S153
14 BAA01g15330 A01 7364462 C T missense_variant MODERATE c.403C>T|p.Pro135Ser S16
15 BAA01g15330 A01 7367283 C T downstream_gene_variant MODIFIER c.*2723C>T| S201
16 BAA01g15330 A01 7368105 C T downstream_gene_variant MODIFIER c.*3545C>T| S4
17 BAA01g15330 A01 7368126 C T downstream_gene_variant MODIFIER c.*3566C>T| S303
18 BAA01g15330 A01 7369313 G A downstream_gene_variant MODIFIER c.*4753G>A| S149