| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID | 
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g32020 | A07 | 31586131 | G | A | upstream_gene_variant | MODIFIER | c.-3666G>A| | S242 | 
| 2 | BAA07g32020 | A07 | 31588172 | G | A | upstream_gene_variant | MODIFIER | c.-1625G>A| | S278 | 
| 3 | BAA07g32020 | A07 | 31588884 | C | T | upstream_gene_variant | MODIFIER | c.-913C>T| | S63 | 
| 4 | BAA07g32020 | A07 | 31589710 | G | A | upstream_gene_variant | MODIFIER | c.-87G>A| | S296 | 
| 5 | BAA07g32020 | A07 | 31590073 | G | A | missense_variant | MODERATE | c.277G>A|p.Glu93Lys | S95 | 
| 6 | BAA07g32020 | A07 | 31590481 | G | A | missense_variant | MODERATE | c.685G>A|p.Val229Ile | S53 | 
| 7 | BAA07g32020 | A07 | 31590797 | C | T | missense_variant | MODERATE | c.1001C>T|p.Ala334Val | S4 | 
| 8 | BAA07g32020 | A07 | 31591112 | C | T | missense_variant | MODERATE | c.1316C>T|p.Thr439Ile | S187 S276 | 
| 9 | BAA07g32020 | A07 | 31591901 | G | A | missense_variant | MODERATE | c.2105G>A|p.Gly702Asp | S206 S26 | 
| 10 | BAA07g32020 | A07 | 31592436 | G | A | synonymous_variant | LOW | c.2565G>A|p.Gln855Gln | S163 | 
| 11 | BAA07g32020 | A07 | 31592494 | C | T | missense_variant | MODERATE | c.2623C>T|p.Pro875Ser | S252 | 
| 12 | BAA07g32020 | A07 | 31592770 | C | T | downstream_gene_variant | MODIFIER | c.*67C>T| | S241 | 
| 13 | BAA07g32020 | A07 | 31593478 | G | A | downstream_gene_variant | MODIFIER | c.*775G>A| | S163 | 
| 14 | BAA07g32020 | A07 | 31594439 | G | T | downstream_gene_variant | MODIFIER | c.*1736G>T| | S160 S235 S260 | 
| 15 | BAA07g32020 | A07 | 31595869 | C | T | downstream_gene_variant | MODIFIER | c.*3166C>T| | S213 | 
| 16 | BAA07g32020 | A07 | 31596822 | G | A | downstream_gene_variant | MODIFIER | c.*4119G>A| | S127 S129 S286 S287 S57 | 
| 17 | BAA07g32020 | A07 | 31597308 | C | T | downstream_gene_variant | MODIFIER | c.*4605C>T| | S270 |