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


Gene ID

Results: 1 - 14 of 14 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA07g01490 A07 1089813 C T upstream_gene_variant MODIFIER c.-4852C>T| S205
2 BAA07g01490 A07 1091579 G A upstream_gene_variant MODIFIER c.-3086G>A| S257
3 BAA07g01490 A07 1093080 C T upstream_gene_variant MODIFIER c.-1585C>T| S205
4 BAA07g01490 A07 1095629 G A missense_variant MODERATE c.506G>A|p.Gly169Glu S296
5 BAA07g01490 A07 1097042 G A synonymous_variant LOW c.1410G>A|p.Val470Val S175
6 BAA07g01490 A07 1097618 C T synonymous_variant LOW c.1902C>T|p.Tyr634Tyr S284
7 BAA07g01490 A07 1098295 C T downstream_gene_variant MODIFIER c.*4C>T| S230
8 BAA07g01490 A07 1099988 C T downstream_gene_variant MODIFIER c.*1697C>T| S97
9 BAA07g01490 A07 1100154 G A downstream_gene_variant MODIFIER c.*1863G>A| S166
10 BAA07g01490 A07 1100863 C T downstream_gene_variant MODIFIER c.*2572C>T| S59
11 BAA07g01490 A07 1101389 G A downstream_gene_variant MODIFIER c.*3098G>A| S180
12 BAA07g01490 A07 1101737 C T downstream_gene_variant MODIFIER c.*3446C>T| S34
13 BAA07g01490 A07 1101829 G A downstream_gene_variant MODIFIER c.*3538G>A| S246
14 BAA07g01490 A07 1101951 C T downstream_gene_variant MODIFIER c.*3660C>T| S77