| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g57260 | A09 | 56597587 | G | A | synonymous_variant | LOW | c.27G>A|p.Arg9Arg |
S263 |
| 2 | BAA09g57260 | A09 | 56597673 | C | T | missense_variant | MODERATE | c.113C>T|p.Thr38Ile |
S207 |
| 3 | BAA09g57260 | A09 | 56597675 | C | T | synonymous_variant | LOW | c.115C>T|p.Leu39Leu |
S157 |
| 4 | BAA09g57260 | A09 | 56598467 | G | A | synonymous_variant | LOW | c.579G>A|p.Lys193Lys |
S181 |
| 5 | BAA09g57260 | A09 | 56599098 | C | T | splice_region_variant&intron_variant | LOW | c.864+8C>T| |
S139 |
| 6 | BAA09g57260 | A09 | 56599510 | G | A | missense_variant | MODERATE | c.1070G>A|p.Gly357Glu |
S295 |
| 7 | BAA09g57260 | A09 | 56599719 | G | A | missense_variant | MODERATE | c.1189G>A|p.Glu397Lys |
S189 |
| 8 | BAA09g57260 | A09 | 56600627 | C | T | synonymous_variant | LOW | c.1864C>T|p.Leu622Leu |
S192 |