| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g41340 | A02 | 34668781 | C | T | synonymous_variant | LOW | c.3351G>A|p.Ala1117Ala |
S179 |
| 2 | BAA02g41340 | A02 | 34668995 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.3211-1G>A| |
S18 |
| 3 | BAA02g41340 | A02 | 34671496 | C | T | missense_variant | MODERATE | c.1561G>A|p.Ala521Thr |
S130 |
| 4 | BAA02g41340 | A02 | 34672336 | G | A | intron_variant | MODIFIER | c.838-18C>T| |
S298 |
| 5 | BAA02g41340 | A02 | 34672549 | G | A | intron_variant | MODIFIER | c.751-42C>T| |
S155 S211 |
| 6 | BAA02g41340 | A02 | 34672820 | C | T | missense_variant | MODERATE | c.631G>A|p.Val211Ile |
S249 |
| 7 | BAA02g41340 | A02 | 34673093 | C | T | intron_variant | MODIFIER | c.508-150G>A| |
S124 |
| 8 | BAA02g41340 | A02 | 34673804 | C | T | synonymous_variant | LOW | c.186G>A|p.Ala62Ala |
S239 S50 |
| 9 | BAA02g41340 | A02 | 34673848 | C | T | missense_variant | MODERATE | c.142G>A|p.Glu48Lys |
S206 |
| 10 | BAA02g41340 | A02 | 34674226 | C | T | upstream_gene_variant | MODIFIER | c.-85G>A| |
S87 |
| 11 | BAA02g41340 | A02 | 34674939 | G | A | upstream_gene_variant | MODIFIER | c.-798C>T| |
S199 |
| 12 | BAA02g41340 | A02 | 34675120 | G | A | upstream_gene_variant | MODIFIER | c.-979C>T| |
S269 |
| 13 | BAA02g41340 | A02 | 34675718 | C | T | upstream_gene_variant | MODIFIER | c.-1577G>A| |
S113 S117 S23 S266 S65 S9 |
| 14 | BAA02g41340 | A02 | 34675776 | C | T | upstream_gene_variant | MODIFIER | c.-1635G>A| |
S80 |
| 15 | BAA02g41340 | A02 | 34676060 | G | A | upstream_gene_variant | MODIFIER | c.-1919C>T| |
S56 |
| 16 | BAA02g41340 | A02 | 34676077 | G | A | upstream_gene_variant | MODIFIER | c.-1936C>T| |
S169 |
| 17 | BAA02g41340 | A02 | 34677306 | G | A | upstream_gene_variant | MODIFIER | c.-3165C>T| |
S306 S308 |
| 18 | BAA02g41340 | A02 | 34678876 | G | A | upstream_gene_variant | MODIFIER | c.-4735C>T| |
S142 |