| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g36660 | A01 | 24519318 | G | A | missense_variant | MODERATE | c.856C>T|p.Pro286Ser |
S203 |
| 2 | BAA01g36660 | A01 | 24519692 | C | T | missense_variant | MODERATE | c.482G>A|p.Arg161Gln |
S115 |
| 3 | BAA01g36660 | A01 | 24519726 | C | T | missense_variant | MODERATE | c.448G>A|p.Val150Met |
S32 |
| 4 | BAA01g36660 | A01 | 24519979 | G | A | synonymous_variant | LOW | c.195C>T|p.Leu65Leu |
S207 |
| 5 | BAA01g36660 | A01 | 24520396 | C | T | upstream_gene_variant | MODIFIER | c.-223G>A| |
S216 |
| 6 | BAA01g36660 | A01 | 24520726 | C | T | upstream_gene_variant | MODIFIER | c.-553G>A| |
S62 |
| 7 | BAA01g36660 | A01 | 24521936 | G | A | upstream_gene_variant | MODIFIER | c.-1763C>T| |
S276 S298 S299 |
| 8 | BAA01g36660 | A01 | 24522727 | G | A | upstream_gene_variant | MODIFIER | c.-2554C>T| |
S267 |
| 9 | BAA01g36660 | A01 | 24523125 | G | A | upstream_gene_variant | MODIFIER | c.-2952C>T| |
S42 |
| 10 | BAA01g36660 | A01 | 24523714 | C | T | upstream_gene_variant | MODIFIER | c.-3541G>A| |
S88 |