| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g01490 | A10 | 747116 | C | T | upstream_gene_variant | MODIFIER | c.-2837C>T| |
S169 |
| 2 | BAA10g01490 | A10 | 750006 | C | T | synonymous_variant | LOW | c.54C>T|p.Arg18Arg |
S131 |
| 3 | BAA10g01490 | A10 | 750841 | G | A | synonymous_variant | LOW | c.354G>A|p.Arg118Arg |
S4 |
| 4 | BAA10g01490 | A10 | 750849 | G | A | missense_variant | MODERATE | c.362G>A|p.Ser121Asn |
S296 |
| 5 | BAA10g01490 | A10 | 750919 | G | A | synonymous_variant | LOW | c.432G>A|p.Glu144Glu |
S150 |