Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g01440 | A09 | 1050276 | G | A | synonymous_variant | LOW | c.573C>T|p.Val191Val |
S232 |
2 | BAA09g01440 | A09 | 1050865 | G | A | upstream_gene_variant | MODIFIER | c.-17C>T| |
S25 |
3 | BAA09g01440 | A09 | 1051695 | C | T | upstream_gene_variant | MODIFIER | c.-847G>A| |
S247 |
4 | BAA09g01440 | A09 | 1052022 | C | T | upstream_gene_variant | MODIFIER | c.-1174G>A| |
S104 S52 |
5 | BAA09g01440 | A09 | 1052180 | G | A | upstream_gene_variant | MODIFIER | c.-1332C>T| |
S99 |
6 | BAA09g01440 | A09 | 1052441 | G | A | upstream_gene_variant | MODIFIER | c.-1593C>T| |
S274 |
7 | BAA09g01440 | A09 | 1054339 | C | T | upstream_gene_variant | MODIFIER | c.-3491G>A| |
S138 |
8 | BAA09g01440 | A09 | 1054346 | G | A | upstream_gene_variant | MODIFIER | c.-3498C>T| |
S138 |
9 | BAA09g01440 | A09 | 1054514 | G | A | upstream_gene_variant | MODIFIER | c.-3666C>T| |
S162 |
10 | BAA09g01440 | A09 | 1054663 | G | A | upstream_gene_variant | MODIFIER | c.-3815C>T| |
S78 S83 |
11 | BAA09g01440 | A09 | 1055107 | C | T | upstream_gene_variant | MODIFIER | c.-4259G>A| |
S54 |