| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g00600 | A10 | 291791 | C | T | missense_variant | MODERATE | c.454G>A|p.Asp152Asn |
S247 |
| 2 | BAA10g00600 | A10 | 292077 | C | T | missense_variant | MODERATE | c.259G>A|p.Ala87Thr |
S255 |
| 3 | BAA10g00600 | A10 | 292108 | G | A | synonymous_variant | LOW | c.228C>T|p.Leu76Leu |
S179 |
| 4 | BAA10g00600 | A10 | 292406 | G | A | missense_variant | MODERATE | c.100C>T|p.Leu34Phe |
S107 |
| 5 | BAA10g00600 | A10 | 292514 | C | T | upstream_gene_variant | MODIFIER | c.-9G>A| |
S297 |
| 6 | BAA10g00600 | A10 | 293409 | A | G | upstream_gene_variant | MODIFIER | c.-904T>C| |
S38 |
| 7 | BAA10g00600 | A10 | 294271 | C | T | upstream_gene_variant | MODIFIER | c.-1766G>A| |
S277 |
| 8 | BAA10g00600 | A10 | 294913 | C | T | upstream_gene_variant | MODIFIER | c.-2408G>A| |
S181 |