Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g10490 | A01 | 4817248 | G | A | downstream_gene_variant | MODIFIER | c.*4137C>T| |
S165 |
2 | BAA01g10490 | A01 | 4817701 | C | T | downstream_gene_variant | MODIFIER | c.*3684G>A| |
S176 |
3 | BAA01g10490 | A01 | 4818557 | C | T | downstream_gene_variant | MODIFIER | c.*2828G>A| |
S255 |
4 | BAA01g10490 | A01 | 4818704 | G | A | downstream_gene_variant | MODIFIER | c.*2681C>T| |
S175 |
5 | BAA01g10490 | A01 | 4819611 | G | A | downstream_gene_variant | MODIFIER | c.*1774C>T| |
S195 |
6 | BAA01g10490 | A01 | 4820009 | C | T | downstream_gene_variant | MODIFIER | c.*1376G>A| |
S286 |
7 | BAA01g10490 | A01 | 4820582 | G | A | downstream_gene_variant | MODIFIER | c.*803C>T| |
S161 |
8 | BAA01g10490 | A01 | 4821174 | C | T | downstream_gene_variant | MODIFIER | c.*211G>A| |
S213 |
9 | BAA01g10490 | A01 | 4821176 | C | T | downstream_gene_variant | MODIFIER | c.*209G>A| |
S68 |
10 | BAA01g10490 | A01 | 4821294 | C | T | downstream_gene_variant | MODIFIER | c.*91G>A| |
S176 |
11 | BAA01g10490 | A01 | 4822820 | G | A | upstream_gene_variant | MODIFIER | c.-1036C>T| |
S188 |
12 | BAA01g10490 | A01 | 4826642 | G | A | upstream_gene_variant | MODIFIER | c.-4858C>T| |
S169 S225 S73 |