| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g20900 | A07 | 25920942 | C | T | missense_variant | MODERATE | c.1258G>A|p.Gly420Arg |
S36 S9 |
| 2 | BAA07g20900 | A07 | 25920970 | C | T | synonymous_variant | LOW | c.1230G>A|p.Ser410Ser |
S261 |
| 3 | BAA07g20900 | A07 | 25922774 | C | T | splice_region_variant&intron_variant | LOW | c.338-4G>A| |
S179 |
| 4 | BAA07g20900 | A07 | 25922984 | C | T | missense_variant | MODERATE | c.208G>A|p.Val70Ile |
S47 |
| 5 | BAA07g20900 | A07 | 25927273 | C | T | upstream_gene_variant | MODIFIER | c.-3693G>A| |
S279 |
| 6 | BAA07g20900 | A07 | 25927615 | C | T | upstream_gene_variant | MODIFIER | c.-4035G>A| |
S262 |
| 7 | BAA07g20900 | A07 | 25927806 | G | A | upstream_gene_variant | MODIFIER | c.-4226C>T| |
S256 |
| 8 | BAA07g20900 | A07 | 25927808 | G | A | upstream_gene_variant | MODIFIER | c.-4228C>T| |
S288 |