| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g34820 | A02 | 29964053 | C | T | missense_variant | MODERATE | c.1799G>A|p.Arg600Lys |
S180 |
| 2 | BAA02g34820 | A02 | 29964403 | C | T | synonymous_variant | LOW | c.1632G>A|p.Glu544Glu |
S118 |
| 3 | BAA02g34820 | A02 | 29965198 | G | A | missense_variant | MODERATE | c.1097C>T|p.Ser366Phe |
S123 |
| 4 | BAA02g34820 | A02 | 29965280 | G | A | missense_variant | MODERATE | c.1015C>T|p.Pro339Ser |
S144 |
| 5 | BAA02g34820 | A02 | 29965411 | G | A | synonymous_variant | LOW | c.975C>T|p.Thr325Thr |
S37 |
| 6 | BAA02g34820 | A02 | 29965719 | G | A | synonymous_variant | LOW | c.744C>T|p.Val248Val |
S235 |
| 7 | BAA02g34820 | A02 | 29966956 | C | T | upstream_gene_variant | MODIFIER | c.-16G>A| |
S157 S163 |
| 8 | BAA02g34820 | A02 | 29968036 | G | A | upstream_gene_variant | MODIFIER | c.-1096C>T| |
S172 S217 |
| 9 | BAA02g34820 | A02 | 29968636 | C | T | upstream_gene_variant | MODIFIER | c.-1696G>A| |
S135 |
| 10 | BAA02g34820 | A02 | 29968868 | C | T | upstream_gene_variant | MODIFIER | c.-1928G>A| |
S301 S304 |
| 11 | BAA02g34820 | A02 | 29968879 | G | A | upstream_gene_variant | MODIFIER | c.-1939C>T| |
S228 |
| 12 | BAA02g34820 | A02 | 29969441 | G | A | upstream_gene_variant | MODIFIER | c.-2501C>T| |
S19 |
| 13 | BAA02g34820 | A02 | 29969674 | C | T | upstream_gene_variant | MODIFIER | c.-2734G>A| |
S296 |
| 14 | BAA02g34820 | A02 | 29969751 | G | A | upstream_gene_variant | MODIFIER | c.-2811C>T| |
S142 |
| 15 | BAA02g34820 | A02 | 29970107 | C | T | upstream_gene_variant | MODIFIER | c.-3167G>A| |
S181 |
| 16 | BAA02g34820 | A02 | 29970383 | G | A | upstream_gene_variant | MODIFIER | c.-3443C>T| |
S7 |
| 17 | BAA02g34820 | A02 | 29971621 | C | T | upstream_gene_variant | MODIFIER | c.-4681G>A| |
S277 |