| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g21960 | A02 | 11813975 | C | T | missense_variant | MODERATE | c.1342G>A|p.Glu448Lys |
S2 |
| 2 | BAA02g21960 | A02 | 11814037 | C | T | missense_variant | MODERATE | c.1280G>A|p.Arg427Gln |
S250 |
| 3 | BAA02g21960 | A02 | 11814260 | C | T | missense_variant | MODERATE | c.1057G>A|p.Glu353Lys |
S284 |
| 4 | BAA02g21960 | A02 | 11814366 | G | A | synonymous_variant | LOW | c.951C>T|p.Ile317Ile |
S156 |
| 5 | BAA02g21960 | A02 | 11814764 | G | A | synonymous_variant | LOW | c.553C>T|p.Leu185Leu |
S129 |
| 6 | BAA02g21960 | A02 | 11814802 | C | T | missense_variant | MODERATE | c.515G>A|p.Ser172Asn |
S80 |
| 7 | BAA02g21960 | A02 | 11814807 | G | A | synonymous_variant | LOW | c.510C>T|p.Ser170Ser |
S50 |
| 8 | BAA02g21960 | A02 | 11815057 | C | T | missense_variant | MODERATE | c.260G>A|p.Gly87Glu |
S305 |
| 9 | BAA02g21960 | A02 | 11816715 | G | A | upstream_gene_variant | MODIFIER | c.-1399C>T| |
S269 |
| 10 | BAA02g21960 | A02 | 11816958 | G | A | upstream_gene_variant | MODIFIER | c.-1642C>T| |
S13 |
| 11 | BAA02g21960 | A02 | 11817746 | C | T | upstream_gene_variant | MODIFIER | c.-2430G>A| |
S167 |
| 12 | BAA02g21960 | A02 | 11818818 | C | T | upstream_gene_variant | MODIFIER | c.-3502G>A| |
S77 S82 |
| 13 | BAA02g21960 | A02 | 11819026 | G | A | upstream_gene_variant | MODIFIER | c.-3710C>T| |
S125 |
| 14 | BAA02g21960 | A02 | 11819432 | C | T | upstream_gene_variant | MODIFIER | c.-4116G>A| |
S77 S82 |
| 15 | BAA02g21960 | A02 | 11819446 | G | A | upstream_gene_variant | MODIFIER | c.-4130C>T| |
S172 S217 |
| 16 | BAA02g21960 | A02 | 11819573 | C | T | upstream_gene_variant | MODIFIER | c.-4257G>A| |
S114 S284 |
| 17 | BAA02g21960 | A02 | 11819803 | C | T | upstream_gene_variant | MODIFIER | c.-4487G>A| |
S221 |
| 18 | BAA02g21960 | A02 | 11820056 | C | T | upstream_gene_variant | MODIFIER | c.-4740G>A| |
S296 |