| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g40690 | A01 | 26929610 | C | T | upstream_gene_variant | MODIFIER | c.-4893C>T| |
S206 S26 |
| 2 | BAA01g40690 | A01 | 26934599 | C | T | missense_variant | MODERATE | c.97C>T|p.Pro33Ser |
S206 S26 |
| 3 | BAA01g40690 | A01 | 26934653 | G | A | missense_variant | MODERATE | c.151G>A|p.Asp51Asn |
S79 S91 |
| 4 | BAA01g40690 | A01 | 26934863 | C | T | missense_variant | MODERATE | c.361C>T|p.Pro121Ser |
S64 |
| 5 | BAA01g40690 | A01 | 26934904 | C | T | synonymous_variant | LOW | c.402C>T|p.Ile134Ile |
S255 |
| 6 | BAA01g40690 | A01 | 26935644 | G | A | synonymous_variant | LOW | c.630G>A|p.Lys210Lys |
S202 |
| 7 | BAA01g40690 | A01 | 26935874 | C | T | synonymous_variant | LOW | c.789C>T|p.Ser263Ser |
S260 |
| 8 | BAA01g40690 | A01 | 26935965 | C | T | missense_variant | MODERATE | c.880C>T|p.Leu294Phe |
S161 |