| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g67190 | A09 | 60999657 | C | T | upstream_gene_variant | MODIFIER | c.-3335C>T| |
S84 S93 |
| 2 | BAA09g67190 | A09 | 61000044 | C | T | upstream_gene_variant | MODIFIER | c.-2948C>T| |
S136 |
| 3 | BAA09g67190 | A09 | 61000618 | C | T | upstream_gene_variant | MODIFIER | c.-2374C>T| |
S269 |
| 4 | BAA09g67190 | A09 | 61001258 | C | T | upstream_gene_variant | MODIFIER | c.-1734C>T| |
S224 |
| 5 | BAA09g67190 | A09 | 61002680 | G | A | upstream_gene_variant | MODIFIER | c.-312G>A| |
S234 |
| 6 | BAA09g67190 | A09 | 61003021 | G | A | synonymous_variant | LOW | c.30G>A|p.Ala10Ala |
S244 |
| 7 | BAA09g67190 | A09 | 61003128 | G | A | missense_variant | MODERATE | c.137G>A|p.Arg46Gln |
S76 |
| 8 | BAA09g67190 | A09 | 61003345 | G | A | synonymous_variant | LOW | c.354G>A|p.Leu118Leu |
S12 |
| 9 | BAA09g67190 | A09 | 61003670 | C | T | missense_variant | MODERATE | c.679C>T|p.Leu227Phe |
S83 S88 |
| 10 | BAA09g67190 | A09 | 61003891 | C | T | synonymous_variant | LOW | c.900C>T|p.Asn300Asn |
S219 S72 |
| 11 | BAA09g67190 | A09 | 61003990 | C | T | synonymous_variant | LOW | c.999C>T|p.Cys333Cys |
S206 S26 |