| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g13890 | A01 | 6587079 | C | T | upstream_gene_variant | MODIFIER | c.-903C>T| |
S112 |
| 2 | BAA01g13890 | A01 | 6587585 | C | T | upstream_gene_variant | MODIFIER | c.-397C>T| |
S208 S93 |
| 3 | BAA01g13890 | A01 | 6589481 | C | T | missense_variant | MODERATE | c.446C>T|p.Pro149Leu |
S1 |
| 4 | BAA01g13890 | A01 | 6590091 | C | T | missense_variant | MODERATE | c.583C>T|p.Arg195Cys |
S125 |
| 5 | BAA01g13890 | A01 | 6590208 | C | T | missense_variant | MODERATE | c.700C>T|p.Leu234Phe |
S206 S26 |
| 6 | BAA01g13890 | A01 | 6590429 | C | T | synonymous_variant | LOW | c.921C>T|p.Pro307Pro |
S47 |
| 7 | BAA01g13890 | A01 | 6592331 | T | C | downstream_gene_variant | MODIFIER | c.*806T>C| |
S292 |
| 8 | BAA01g13890 | A01 | 6593202 | G | A | downstream_gene_variant | MODIFIER | c.*1677G>A| |
S178 |
| 9 | BAA01g13890 | A01 | 6593827 | G | A | downstream_gene_variant | MODIFIER | c.*2302G>A| |
S28 |
| 10 | BAA01g13890 | A01 | 6594958 | G | A | downstream_gene_variant | MODIFIER | c.*3433G>A| |
S163 |