| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g08120 | A05 | 4030083 | G | A | splice_region_variant&intron_variant | LOW | c.2330-7C>T| |
S306 S308 |
| 2 | BAA05g08120 | A05 | 4033872 | G | A | missense_variant | MODERATE | c.1736C>T|p.Ser579Phe |
S192 |
| 3 | BAA05g08120 | A05 | 4034018 | G | A | synonymous_variant | LOW | c.1590C>T|p.Asp530Asp |
S143 |
| 4 | BAA05g08120 | A05 | 4034063 | G | A | synonymous_variant | LOW | c.1545C>T|p.Ile515Ile |
S109 |
| 5 | BAA05g08120 | A05 | 4041588 | C | T | upstream_gene_variant | MODIFIER | c.-2742G>A| |
S107 |
| 6 | BAA05g08120 | A05 | 4042002 | T | C | upstream_gene_variant | MODIFIER | c.-3156A>G| |
S8 |
| 7 | BAA05g08120 | A05 | 4042055 | G | A | upstream_gene_variant | MODIFIER | c.-3209C>T| |
S179 |
| 8 | BAA05g08120 | A05 | 4042378 | G | A | upstream_gene_variant | MODIFIER | c.-3532C>T| |
S127 |
| 9 | BAA05g08120 | A05 | 4042561 | G | A | upstream_gene_variant | MODIFIER | c.-3715C>T| |
S230 |
| 10 | BAA05g08120 | A05 | 4043462 | C | T | upstream_gene_variant | MODIFIER | c.-4616G>A| |
S118 |