| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g08930 | A10 | 10941137 | C | T | missense_variant | MODERATE | c.461G>A|p.Gly154Glu |
S84 S93 |
| 2 | BAA10g08930 | A10 | 10941183 | G | A | intron_variant | MODIFIER | c.427-12C>T| |
S286 |
| 3 | BAA10g08930 | A10 | 10941727 | G | A | synonymous_variant | LOW | c.366C>T|p.Arg122Arg |
S267 |
| 4 | BAA10g08930 | A10 | 10941780 | C | T | missense_variant | MODERATE | c.313G>A|p.Ala105Thr |
S44 |
| 5 | BAA10g08930 | A10 | 10943579 | C | A | upstream_gene_variant | MODIFIER | c.-1487G>T| |
S288 |
| 6 | BAA10g08930 | A10 | 10944334 | G | A | upstream_gene_variant | MODIFIER | c.-2242C>T| |
S296 |
| 7 | BAA10g08930 | A10 | 10944969 | C | T | upstream_gene_variant | MODIFIER | c.-2877G>A| |
S255 |
| 8 | BAA10g08930 | A10 | 10945074 | G | A | upstream_gene_variant | MODIFIER | c.-2982C>T| |
S134 |
| 9 | BAA10g08930 | A10 | 10946049 | G | A | upstream_gene_variant | MODIFIER | c.-3957C>T| |
S219 S301 S72 |
| 10 | BAA10g08930 | A10 | 10946378 | C | T | upstream_gene_variant | MODIFIER | c.-4286G>A| |
S103 |