| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA04g13650 | A04 | 19003010 | C | T | synonymous_variant | LOW | c.75C>T|p.Phe25Phe |
S48 |
| 2 | BAA04g13650 | A04 | 19003351 | G | T | missense_variant | MODERATE | c.416G>T|p.Gly139Val |
S13 S143 S154 S164 S201 S206 S219 S230 S232 S239 S26 S278 S279 S302 S306 S308 S78 |
| 3 | BAA04g13650 | A04 | 19003605 | G | A | missense_variant | MODERATE | c.670G>A|p.Glu224Lys |
S236 |
| 4 | BAA04g13650 | A04 | 19003883 | C | T | synonymous_variant | LOW | c.948C>T|p.Thr316Thr |
S172 S217 |
| 5 | BAA04g13650 | A04 | 19004615 | G | A | synonymous_variant | LOW | c.1680G>A|p.Glu560Glu |
S192 |
| 6 | BAA04g13650 | A04 | 19004853 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1858-1G>A| |
S278 |
| 7 | BAA04g13650 | A04 | 19004898 | C | T | synonymous_variant | LOW | c.1902C>T|p.Val634Val |
S110 |
| 8 | BAA04g13650 | A04 | 19005610 | C | T | missense_variant | MODERATE | c.2614C>T|p.Pro872Ser |
S4 |
| 9 | BAA04g13650 | A04 | 19005731 | C | T | missense_variant | MODERATE | c.2735C>T|p.Ala912Val |
S132 S137 S215 S89 |
| 10 | BAA04g13650 | A04 | 19005772 | G | A | missense_variant | MODERATE | c.2776G>A|p.Val926Met |
S13 |