Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17930 | A02 | 9008238 | G | A | missense_variant | MODERATE | c.92C>T|p.Ser31Phe |
S274 |
2 | BAA02g17930 | A02 | 9011981 | C | T | upstream_gene_variant | MODIFIER | c.-551G>A| |
S8 |
3 | BAA02g17930 | A02 | 9013558 | G | A | upstream_gene_variant | MODIFIER | c.-2128C>T| |
S59 |
4 | BAA02g17930 | A02 | 9014478 | G | A | upstream_gene_variant | MODIFIER | c.-3048C>T| |
S86 |
5 | BAA02g17930 | A02 | 9014572 | G | A | upstream_gene_variant | MODIFIER | c.-3142C>T| |
S176 |
6 | BAA02g17930 | A02 | 9014581 | C | T | upstream_gene_variant | MODIFIER | c.-3151G>A| |
S273 |
7 | BAA02g17930 | A02 | 9015290 | G | A | upstream_gene_variant | MODIFIER | c.-3860C>T| |
S95 |
8 | BAA02g17930 | A02 | 9015544 | G | A | upstream_gene_variant | MODIFIER | c.-4114C>T| |
S299 |
9 | BAA02g17930 | A02 | 9015644 | G | A | upstream_gene_variant | MODIFIER | c.-4214C>T| |
S190 |
10 | BAA02g17930 | A02 | 9016298 | C | T | upstream_gene_variant | MODIFIER | c.-4868G>A| |
S87 |