| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g02900 | A05 | 1506714 | T | G | missense_variant | MODERATE | c.775A>C|p.Ser259Arg |
S1 S105 S114 S118 S127 S137 S139 S165 S193 S194 S263 S27 S270 S280 S33 S4 S45 S90 S94 |
| 2 | BAA05g02900 | A05 | 1506739 | G | A | synonymous_variant | LOW | c.750C>T|p.Phe250Phe |
S67 |
| 3 | BAA05g02900 | A05 | 1506942 | G | A | missense_variant | MODERATE | c.547C>T|p.Pro183Ser |
S159 S243 |
| 4 | BAA05g02900 | A05 | 1507193 | G | A | missense_variant | MODERATE | c.296C>T|p.Thr99Met |
S33 |
| 5 | BAA05g02900 | A05 | 1507233 | C | T | missense_variant | MODERATE | c.256G>A|p.Ala86Thr |
S2 |
| 6 | BAA05g02900 | A05 | 1510736 | G | A | upstream_gene_variant | MODIFIER | c.-3248C>T| |
S25 S264 |
| 7 | BAA05g02900 | A05 | 1510895 | C | T | upstream_gene_variant | MODIFIER | c.-3407G>A| |
S127 |