| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g16120 | A10 | 16105794 | C | T | missense_variant | MODERATE | c.1210G>A|p.Glu404Lys |
S196 |
| 2 | BAA10g16120 | A10 | 16106468 | G | A | missense_variant | MODERATE | c.536C>T|p.Ala179Val |
S293 |
| 3 | BAA10g16120 | A10 | 16107113 | C | T | upstream_gene_variant | MODIFIER | c.-110G>A| |
S123 |
| 4 | BAA10g16120 | A10 | 16107281 | C | T | upstream_gene_variant | MODIFIER | c.-278G>A| |
S169 |
| 5 | BAA10g16120 | A10 | 16108487 | G | A | upstream_gene_variant | MODIFIER | c.-1484C>T| |
S50 |
| 6 | BAA10g16120 | A10 | 16109693 | G | A | upstream_gene_variant | MODIFIER | c.-2690C>T| |
S1 S228 S244 S251 S90 |
| 7 | BAA10g16120 | A10 | 16109709 | G | A | upstream_gene_variant | MODIFIER | c.-2706C>T| |
S132 S137 S215 |
| 8 | BAA10g16120 | A10 | 16111153 | C | T | upstream_gene_variant | MODIFIER | c.-4150G>A| |
S298 |
| 9 | BAA10g16120 | A10 | 16111940 | C | T | upstream_gene_variant | MODIFIER | c.-4937G>A| |
S283 |
| 10 | BAA10g16120 | A10 | 16111952 | C | T | upstream_gene_variant | MODIFIER | c.-4949G>A| |
S283 |