Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g04760 | A04 | 3001034 | G | A | downstream_gene_variant | MODIFIER | c.*3981C>T| |
S143 |
2 | BAA04g04760 | A04 | 3001582 | C | T | downstream_gene_variant | MODIFIER | c.*3433G>A| |
S122 |
3 | BAA04g04760 | A04 | 3001776 | G | A | downstream_gene_variant | MODIFIER | c.*3239C>T| |
S5 |
4 | BAA04g04760 | A04 | 3001980 | G | A | downstream_gene_variant | MODIFIER | c.*3035C>T| |
S167 |
5 | BAA04g04760 | A04 | 3002543 | C | T | downstream_gene_variant | MODIFIER | c.*2472G>A| |
S296 |
6 | BAA04g04760 | A04 | 3002786 | C | T | downstream_gene_variant | MODIFIER | c.*2229G>A| |
S296 S33 |
7 | BAA04g04760 | A04 | 3003746 | C | T | downstream_gene_variant | MODIFIER | c.*1269G>A| |
S296 |
8 | BAA04g04760 | A04 | 3003785 | C | T | downstream_gene_variant | MODIFIER | c.*1230G>A| |
S293 |
9 | BAA04g04760 | A04 | 3005682 | G | A | missense_variant | MODERATE | c.272C>T|p.Ala91Val |
S144 |
10 | BAA04g04760 | A04 | 3006357 | C | T | upstream_gene_variant | MODIFIER | c.-404G>A| |
S92 |