| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g20740 | A07 | 25850838 | G | A | upstream_gene_variant | MODIFIER | c.-1386G>A| |
S132 S137 S215 S89 |
| 2 | BAA07g20740 | A07 | 25850906 | G | A | upstream_gene_variant | MODIFIER | c.-1318G>A| |
S6 |
| 3 | BAA07g20740 | A07 | 25851127 | G | A | upstream_gene_variant | MODIFIER | c.-1097G>A| |
S157 S163 |
| 4 | BAA07g20740 | A07 | 25851455 | C | T | upstream_gene_variant | MODIFIER | c.-769C>T| |
S274 |
| 5 | BAA07g20740 | A07 | 25851990 | G | A | upstream_gene_variant | MODIFIER | c.-234G>A| |
S235 |
| 6 | BAA07g20740 | A07 | 25852830 | G | A | missense_variant | MODERATE | c.607G>A|p.Glu203Lys |
S237 |
| 7 | BAA07g20740 | A07 | 25852853 | C | T | synonymous_variant | LOW | c.630C>T|p.Thr210Thr |
S244 |
| 8 | BAA07g20740 | A07 | 25853379 | C | T | intron_variant | MODIFIER | c.888+268C>T| |
S284 |
| 9 | BAA07g20740 | A07 | 25854193 | G | A | missense_variant | MODERATE | c.1310G>A|p.Gly437Glu |
S59 |
| 10 | BAA07g20740 | A07 | 25854484 | C | T | downstream_gene_variant | MODIFIER | c.*98C>T| |
S305 |
| 11 | BAA07g20740 | A07 | 25855827 | G | A | downstream_gene_variant | MODIFIER | c.*1441G>A| |
S292 |