| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g58560 | A09 | 57208316 | G | A | missense_variant | MODERATE | c.106G>A|p.Ala36Thr |
S2 |
| 2 | BAA09g58560 | A09 | 57208320 | C | T | missense_variant | MODERATE | c.110C>T|p.Ala37Val |
S61 |
| 3 | BAA09g58560 | A09 | 57208340 | G | A | missense_variant | MODERATE | c.130G>A|p.Asp44Asn |
S115 |
| 4 | BAA09g58560 | A09 | 57208377 | C | T | missense_variant | MODERATE | c.167C>T|p.Ser56Phe |
S238 |
| 5 | BAA09g58560 | A09 | 57208594 | C | T | synonymous_variant | LOW | c.384C>T|p.Ser128Ser |
S223 |
| 6 | BAA09g58560 | A09 | 57208612 | C | T | splice_region_variant&intron_variant | LOW | c.394+8C>T| |
S136 |
| 7 | BAA09g58560 | A09 | 57208829 | G | A | missense_variant | MODERATE | c.538G>A|p.Asp180Asn |
S36 |
| 8 | BAA09g58560 | A09 | 57209013 | G | A | missense_variant | MODERATE | c.722G>A|p.Gly241Glu |
S42 |