Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44150 | A02 | 36432883 | G | A | upstream_gene_variant | MODIFIER | c.-4817G>A| |
S302 |
2 | BAA02g44150 | A02 | 36432981 | G | A | upstream_gene_variant | MODIFIER | c.-4719G>A| |
S84 |
3 | BAA02g44150 | A02 | 36433336 | G | A | upstream_gene_variant | MODIFIER | c.-4364G>A| |
S293 |
4 | BAA02g44150 | A02 | 36435584 | C | T | upstream_gene_variant | MODIFIER | c.-2116C>T| |
S3 |
5 | BAA02g44150 | A02 | 36436354 | G | A | upstream_gene_variant | MODIFIER | c.-1346G>A| |
S292 |
6 | BAA02g44150 | A02 | 36436819 | G | A | upstream_gene_variant | MODIFIER | c.-881G>A| |
S291 |
7 | BAA02g44150 | A02 | 36437540 | C | T | upstream_gene_variant | MODIFIER | c.-160C>T| |
S308 |
8 | BAA02g44150 | A02 | 36437900 | C | T | intron_variant | MODIFIER | c.162+39C>T| |
S210 |
9 | BAA02g44150 | A02 | 36438798 | C | T | missense_variant | MODERATE | c.266C>T|p.Ala89Val |
S144 |
10 | BAA02g44150 | A02 | 36439096 | C | T | synonymous_variant | LOW | c.564C>T|p.Tyr188Tyr |
S221 |
11 | BAA02g44150 | A02 | 36440291 | C | T | downstream_gene_variant | MODIFIER | c.*1021C>T| |
S271 |
12 | BAA02g44150 | A02 | 36440682 | G | A | downstream_gene_variant | MODIFIER | c.*1412G>A| |
S169 |
13 | BAA02g44150 | A02 | 36442342 | C | T | downstream_gene_variant | MODIFIER | c.*3072C>T| |
S249 |
14 | BAA02g44150 | A02 | 36442448 | G | A | downstream_gene_variant | MODIFIER | c.*3178G>A| |
S232 |
15 | BAA02g44150 | A02 | 36442459 | G | C | downstream_gene_variant | MODIFIER | c.*3189G>C| |
S130 |