| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g10960 | A05 | 5580412 | C | T | upstream_gene_variant | MODIFIER | c.-3051C>T| |
S163 |
| 2 | BAA05g10960 | A05 | 5581621 | G | A | upstream_gene_variant | MODIFIER | c.-1842G>A| |
S241 |
| 3 | BAA05g10960 | A05 | 5581751 | C | T | upstream_gene_variant | MODIFIER | c.-1712C>T| |
S18 |
| 4 | BAA05g10960 | A05 | 5583174 | G | A | upstream_gene_variant | MODIFIER | c.-289G>A| |
S122 |
| 5 | BAA05g10960 | A05 | 5584092 | C | T | synonymous_variant | LOW | c.630C>T|p.Leu210Leu |
S167 |
| 6 | BAA05g10960 | A05 | 5584251 | G | A | missense_variant | MODERATE | c.789G>A|p.Met263Ile |
S173 |
| 7 | BAA05g10960 | A05 | 5584269 | G | A | synonymous_variant | LOW | c.807G>A|p.Glu269Glu |
S85 |
| 8 | BAA05g10960 | A05 | 5584607 | C | T | missense_variant | MODERATE | c.1145C>T|p.Pro382Leu |
S193 |