| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA06g08590 | A06 | 4401195 | C | T | missense_variant | MODERATE | c.1079G>A|p.Arg360Lys |
S135 |
| 2 | BAA06g08590 | A06 | 4401257 | C | T | synonymous_variant | LOW | c.1017G>A|p.Leu339Leu |
S216 |
| 3 | BAA06g08590 | A06 | 4401319 | C | T | missense_variant | MODERATE | c.955G>A|p.Asp319Asn |
S199 |
| 4 | BAA06g08590 | A06 | 4401868 | C | T | missense_variant | MODERATE | c.406G>A|p.Asp136Asn |
S263 |
| 5 | BAA06g08590 | A06 | 4403997 | C | T | upstream_gene_variant | MODIFIER | c.-1490G>A| |
S250 |
| 6 | BAA06g08590 | A06 | 4404585 | C | T | upstream_gene_variant | MODIFIER | c.-2078G>A| |
S56 |
| 7 | BAA06g08590 | A06 | 4404805 | G | A | upstream_gene_variant | MODIFIER | c.-2298C>T| |
S82 S92 |
| 8 | BAA06g08590 | A06 | 4405768 | G | A | upstream_gene_variant | MODIFIER | c.-3261C>T| |
S127 S187 |