Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g00780 | A01 | 352151 | C | T | downstream_gene_variant | MODIFIER | c.*4823G>A| |
S77 S82 |
2 | BAA01g00780 | A01 | 352194 | G | A | downstream_gene_variant | MODIFIER | c.*4780C>T| |
S183 S198 |
3 | BAA01g00780 | A01 | 352304 | G | A | downstream_gene_variant | MODIFIER | c.*4670C>T| |
S9 |
4 | BAA01g00780 | A01 | 353244 | G | A | downstream_gene_variant | MODIFIER | c.*3730C>T| |
S197 |
5 | BAA01g00780 | A01 | 353560 | G | A | downstream_gene_variant | MODIFIER | c.*3414C>T| |
S308 |
6 | BAA01g00780 | A01 | 353882 | G | A | downstream_gene_variant | MODIFIER | c.*3092C>T| |
S172 S217 |
7 | BAA01g00780 | A01 | 354133 | C | T | downstream_gene_variant | MODIFIER | c.*2841G>A| |
S182 |
8 | BAA01g00780 | A01 | 354355 | C | T | downstream_gene_variant | MODIFIER | c.*2619G>A| |
S278 |
9 | BAA01g00780 | A01 | 356796 | G | A | downstream_gene_variant | MODIFIER | c.*178C>T| |
S136 |
10 | BAA01g00780 | A01 | 357654 | G | A | missense_variant | MODERATE | c.151C>T|p.Leu51Phe |
S294 |
11 | BAA01g00780 | A01 | 360359 | C | T | upstream_gene_variant | MODIFIER | c.-2555G>A| |
S137 |
12 | BAA01g00780 | A01 | 361256 | G | A | upstream_gene_variant | MODIFIER | c.-3452C>T| |
S168 |
13 | BAA01g00780 | A01 | 361513 | C | T | upstream_gene_variant | MODIFIER | c.-3709G>A| |
S130 |