| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g29140 | A10 | 22040696 | C | T | upstream_gene_variant | MODIFIER | c.-311C>T| |
S187 |
| 2 | BAA10g29140 | A10 | 22040743 | G | A | upstream_gene_variant | MODIFIER | c.-264G>A| |
S35 |
| 3 | BAA10g29140 | A10 | 22041012 | C | T | synonymous_variant | LOW | c.6C>T|p.Ser2Ser |
S44 |
| 4 | BAA10g29140 | A10 | 22041147 | C | T | synonymous_variant | LOW | c.141C>T|p.Thr47Thr |
S282 |
| 5 | BAA10g29140 | A10 | 22041334 | G | A | missense_variant | MODERATE | c.328G>A|p.Asp110Asn |
S298 |
| 6 | BAA10g29140 | A10 | 22042945 | G | A | missense_variant | MODERATE | c.964G>A|p.Asp322Asn |
S62 |
| 7 | BAA10g29140 | A10 | 22043148 | G | A | missense_variant | MODERATE | c.1087G>A|p.Glu363Lys |
S296 |
| 8 | BAA10g29140 | A10 | 22045939 | C | T | downstream_gene_variant | MODIFIER | c.*1167C>T| |
S166 |
| 9 | BAA10g29140 | A10 | 22046353 | C | G | downstream_gene_variant | MODIFIER | c.*1581C>G| |
S120 |
| 10 | BAA10g29140 | A10 | 22047244 | G | A | downstream_gene_variant | MODIFIER | c.*2472G>A| |
S173 |
| 11 | BAA10g29140 | A10 | 22048640 | G | A | downstream_gene_variant | MODIFIER | c.*3868G>A| |
S127 |