| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g06000 | A01 | 2689981 | G | A | missense_variant | MODERATE | c.1865C>T|p.Ser622Phe |
S13 |
| 2 | BAA01g06000 | A01 | 2691372 | G | A | missense_variant | MODERATE | c.1021C>T|p.Pro341Ser |
S180 |
| 3 | BAA01g06000 | A01 | 2693254 | A | T | upstream_gene_variant | MODIFIER | c.-276T>A| |
S153 S213 |
| 4 | BAA01g06000 | A01 | 2696513 | G | A | upstream_gene_variant | MODIFIER | c.-3535C>T| |
S157 S163 |
| 5 | BAA01g06000 | A01 | 2697705 | G | T | upstream_gene_variant | MODIFIER | c.-4727C>A| |
S305 S5 |
| 6 | BAA01g06000 | A01 | 2697754 | C | T | upstream_gene_variant | MODIFIER | c.-4776G>A| |
S69 |
| 7 | BAA01g06000 | A01 | 2697783 | A | C | upstream_gene_variant | MODIFIER | c.-4805T>G| |
S170 S191 S193 S229 |
| 8 | BAA01g06000 | A01 | 2697784 | A | C | upstream_gene_variant | MODIFIER | c.-4806T>G| |
S135 S165 S170 S171 S191 S193 S211 S229 S3 |