| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g40300 | A05 | 39030704 | G | A | synonymous_variant | LOW | c.2814C>T|p.Leu938Leu |
S200 |
| 2 | BAA05g40300 | A05 | 39031380 | G | A | missense_variant | MODERATE | c.2375C>T|p.Pro792Leu |
S213 |
| 3 | BAA05g40300 | A05 | 39033519 | C | T | missense_variant | MODERATE | c.890G>A|p.Arg297Lys |
S241 |
| 4 | BAA05g40300 | A05 | 39033607 | C | T | missense_variant | MODERATE | c.802G>A|p.Glu268Lys |
S269 |
| 5 | BAA05g40300 | A05 | 39035419 | C | T | upstream_gene_variant | MODIFIER | c.-384G>A| |
S36 |
| 6 | BAA05g40300 | A05 | 39035508 | G | A | upstream_gene_variant | MODIFIER | c.-473C>T| |
S203 |
| 7 | BAA05g40300 | A05 | 39035511 | G | A | upstream_gene_variant | MODIFIER | c.-476C>T| |
S245 |
| 8 | BAA05g40300 | A05 | 39035821 | C | T | upstream_gene_variant | MODIFIER | c.-786G>A| |
S223 |
| 9 | BAA05g40300 | A05 | 39036432 | G | A | upstream_gene_variant | MODIFIER | c.-1397C>T| |
S279 |
| 10 | BAA05g40300 | A05 | 39037704 | G | A | upstream_gene_variant | MODIFIER | c.-2669C>T| |
S171 |
| 11 | BAA05g40300 | A05 | 39039000 | C | T | upstream_gene_variant | MODIFIER | c.-3965G>A| |
S192 |