| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g41100 | A09 | 47939881 | G | A | missense_variant | MODERATE | c.716C>T|p.Thr239Ile |
S25 |
| 2 | BAA09g41100 | A09 | 47939883 | G | A | synonymous_variant | LOW | c.714C>T|p.Asn238Asn |
S262 |
| 3 | BAA09g41100 | A09 | 47940594 | C | G | missense_variant | MODERATE | c.313G>C|p.Gly105Arg |
S26 |
| 4 | BAA09g41100 | A09 | 47941442 | C | T | upstream_gene_variant | MODIFIER | c.-412G>A| |
S192 S247 |
| 5 | BAA09g41100 | A09 | 47941559 | G | A | upstream_gene_variant | MODIFIER | c.-529C>T| |
S4 |
| 6 | BAA09g41100 | A09 | 47944732 | C | T | upstream_gene_variant | MODIFIER | c.-3702G>A| |
S206 S26 |
| 7 | BAA09g41100 | A09 | 47945982 | G | A | upstream_gene_variant | MODIFIER | c.-4952C>T| |
S281 |