| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g19770 | A10 | 18020435 | C | T | synonymous_variant | LOW | c.3006G>A|p.Gln1002Gln |
S180 |
| 2 | BAA10g19770 | A10 | 18020776 | C | T | missense_variant | MODERATE | c.2665G>A|p.Ala889Thr |
S123 |
| 3 | BAA10g19770 | A10 | 18023734 | C | T | missense_variant | MODERATE | c.301G>A|p.Glu101Lys |
S200 |
| 4 | BAA10g19770 | A10 | 18024863 | G | A | upstream_gene_variant | MODIFIER | c.-748C>T| |
S267 |
| 5 | BAA10g19770 | A10 | 18025544 | C | T | upstream_gene_variant | MODIFIER | c.-1429G>A| |
S133 |
| 6 | BAA10g19770 | A10 | 18026572 | C | T | upstream_gene_variant | MODIFIER | c.-2457G>A| |
S121 |