| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA03g61130 | A03 | 30865194 | G | A | upstream_gene_variant | MODIFIER | c.-4853G>A| |
S5 |
| 2 | BAA03g61130 | A03 | 30865737 | G | A | upstream_gene_variant | MODIFIER | c.-4310G>A| |
S132 S137 S215 S89 |
| 3 | BAA03g61130 | A03 | 30865960 | C | T | upstream_gene_variant | MODIFIER | c.-4087C>T| |
S59 |
| 4 | BAA03g61130 | A03 | 30867511 | C | T | upstream_gene_variant | MODIFIER | c.-2536C>T| |
S134 |
| 5 | BAA03g61130 | A03 | 30869115 | G | A | upstream_gene_variant | MODIFIER | c.-932G>A| |
S291 |
| 6 | BAA03g61130 | A03 | 30870065 | C | T | missense_variant | MODERATE | c.19C>T|p.Pro7Ser |
S273 |
| 7 | BAA03g61130 | A03 | 30871249 | C | T | synonymous_variant | LOW | c.1203C>T|p.Asn401Asn |
S77 |
| 8 | BAA03g61130 | A03 | 30871292 | C | T | stop_gained | HIGH | c.1246C>T|p.Arg416* |
S35 |
| 9 | BAA03g61130 | A03 | 30872379 | G | A | missense_variant | MODERATE | c.1876G>A|p.Glu626Lys |
S85 |
| 10 | BAA03g61130 | A03 | 30874627 | C | T | downstream_gene_variant | MODIFIER | c.*2138C>T| |
S231 |
| 11 | BAA03g61130 | A03 | 30874659 | C | T | downstream_gene_variant | MODIFIER | c.*2170C>T| |
S78 |
| 12 | BAA03g61130 | A03 | 30875173 | T | C | downstream_gene_variant | MODIFIER | c.*2684T>C| |
S235 |
| 13 | BAA03g61130 | A03 | 30876664 | C | T | downstream_gene_variant | MODIFIER | c.*4175C>T| |
S140 |
| 14 | BAA03g61130 | A03 | 30876786 | G | A | downstream_gene_variant | MODIFIER | c.*4297G>A| |
S69 |
| 15 | BAA03g61130 | A03 | 30876850 | C | T | downstream_gene_variant | MODIFIER | c.*4361C>T| |
S263 |
| 16 | BAA03g61130 | A03 | 30876928 | G | A | downstream_gene_variant | MODIFIER | c.*4439G>A| |
S114 |
| 17 | BAA03g61130 | A03 | 30877377 | C | T | downstream_gene_variant | MODIFIER | c.*4888C>T| |
S159 |