| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g17730 | A10 | 16907467 | G | A | upstream_gene_variant | MODIFIER | c.-1372G>A| |
S42 |
| 2 | BAA10g17730 | A10 | 16909589 | G | A | missense_variant | MODERATE | c.598G>A|p.Val200Met |
S202 |
| 3 | BAA10g17730 | A10 | 16910259 | C | T | missense_variant | MODERATE | c.1181C>T|p.Ser394Phe |
S142 |
| 4 | BAA10g17730 | A10 | 16910321 | G | A | missense_variant | MODERATE | c.1243G>A|p.Val415Ile |
S43 |
| 5 | BAA10g17730 | A10 | 16911106 | G | A | missense_variant | MODERATE | c.1853G>A|p.Arg618Lys |
S192 |
| 6 | BAA10g17730 | A10 | 16914005 | G | A | downstream_gene_variant | MODIFIER | c.*2877G>A| |
S221 |
| 7 | BAA10g17730 | A10 | 16914155 | C | T | downstream_gene_variant | MODIFIER | c.*3027C>T| |
S281 |
| 8 | BAA10g17730 | A10 | 16914857 | C | T | downstream_gene_variant | MODIFIER | c.*3729C>T| |
S117 |