Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10490 | A02 | 4653777 | G | A | missense_variant | MODERATE | c.76C>T|p.Leu26Phe |
S205 |
2 | BAA02g10490 | A02 | 4654014 | G | A | upstream_gene_variant | MODIFIER | c.-162C>T| |
S148 S30 S31 |
3 | BAA02g10490 | A02 | 4654184 | G | A | upstream_gene_variant | MODIFIER | c.-332C>T| |
S244 |
4 | BAA02g10490 | A02 | 4654837 | G | A | upstream_gene_variant | MODIFIER | c.-985C>T| |
S98 |
5 | BAA02g10490 | A02 | 4655221 | C | T | upstream_gene_variant | MODIFIER | c.-1369G>A| |
S3 |
6 | BAA02g10490 | A02 | 4655271 | C | T | upstream_gene_variant | MODIFIER | c.-1419G>A| |
S128 |
7 | BAA02g10490 | A02 | 4655354 | G | A | upstream_gene_variant | MODIFIER | c.-1502C>T| |
S286 |
8 | BAA02g10490 | A02 | 4657303 | G | A | upstream_gene_variant | MODIFIER | c.-3451C>T| |
S265 |