Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g26980 | A01 | 15256286 | C | T | upstream_gene_variant | MODIFIER | c.-2839C>T| |
S150 |
2 | BAA01g26980 | A01 | 15256445 | C | T | upstream_gene_variant | MODIFIER | c.-2680C>T| |
S48 |
3 | BAA01g26980 | A01 | 15258397 | G | A | upstream_gene_variant | MODIFIER | c.-728G>A| |
S97 |
4 | BAA01g26980 | A01 | 15258551 | G | A | upstream_gene_variant | MODIFIER | c.-574G>A| |
S70 |
5 | BAA01g26980 | A01 | 15258562 | C | T | upstream_gene_variant | MODIFIER | c.-563C>T| |
S134 |
6 | BAA01g26980 | A01 | 15259684 | C | T | intron_variant | MODIFIER | c.513+47C>T| |
S305 |
7 | BAA01g26980 | A01 | 15260189 | C | T | intron_variant | MODIFIER | c.513+552C>T| |
S118 |
8 | BAA01g26980 | A01 | 15260608 | G | A | intron_variant | MODIFIER | c.514-240G>A| |
S100 |
9 | BAA01g26980 | A01 | 15262061 | G | A | downstream_gene_variant | MODIFIER | c.*869G>A| |
S193 |
10 | BAA01g26980 | A01 | 15262101 | G | A | downstream_gene_variant | MODIFIER | c.*909G>A| |
S217 |
11 | BAA01g26980 | A01 | 15262177 | G | A | downstream_gene_variant | MODIFIER | c.*985G>A| |
S249 |
12 | BAA01g26980 | A01 | 15262774 | C | T | downstream_gene_variant | MODIFIER | c.*1582C>T| |
S296 |
13 | BAA01g26980 | A01 | 15262820 | C | T | downstream_gene_variant | MODIFIER | c.*1628C>T| |
S249 S38 |