| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g31130 | A10 | 22818652 | C | T | upstream_gene_variant | MODIFIER | c.-690C>T| |
S234 |
| 2 | BAA10g31130 | A10 | 22818675 | C | T | upstream_gene_variant | MODIFIER | c.-667C>T| |
S246 |
| 3 | BAA10g31130 | A10 | 22819391 | C | T | missense_variant | MODERATE | c.50C>T|p.Thr17Ile |
S187 |
| 4 | BAA10g31130 | A10 | 22820261 | C | T | missense_variant | MODERATE | c.736C>T|p.Leu246Phe |
S8 |
| 5 | BAA10g31130 | A10 | 22820264 | C | T | missense_variant | MODERATE | c.739C>T|p.Leu247Phe |
S238 |
| 6 | BAA10g31130 | A10 | 22820931 | G | A | synonymous_variant | LOW | c.1251G>A|p.Lys417Lys |
S66 |
| 7 | BAA10g31130 | A10 | 22820973 | A | C | splice_region_variant&intron_variant | LOW | c.1290+3A>C| |
S86 |
| 8 | BAA10g31130 | A10 | 22821342 | C | T | missense_variant | MODERATE | c.1490C>T|p.Ala497Val |
S20 |