| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g13030 | A01 | 6176451 | C | T | synonymous_variant | LOW | c.1383G>A|p.Leu461Leu |
S295 |
| 2 | BAA01g13030 | A01 | 6176642 | C | T | missense_variant | MODERATE | c.1192G>A|p.Asp398Asn |
S150 |
| 3 | BAA01g13030 | A01 | 6176795 | C | T | missense_variant | MODERATE | c.1039G>A|p.Val347Met |
S284 |
| 4 | BAA01g13030 | A01 | 6177087 | C | T | synonymous_variant | LOW | c.747G>A|p.Lys249Lys |
S125 |
| 5 | BAA01g13030 | A01 | 6177773 | C | T | missense_variant | MODERATE | c.61G>A|p.Asp21Asn |
S255 |
| 6 | BAA01g13030 | A01 | 6177781 | G | A | missense_variant | MODERATE | c.53C>T|p.Ser18Phe |
S175 |
| 7 | BAA01g13030 | A01 | 6178481 | G | A | upstream_gene_variant | MODIFIER | c.-648C>T| |
S178 |
| 8 | BAA01g13030 | A01 | 6179532 | C | T | upstream_gene_variant | MODIFIER | c.-1699G>A| |
S166 |