| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g01690 | A01 | 750157 | G | A | missense_variant | MODERATE | c.1192C>T|p.Pro398Ser |
S98 |
| 2 | BAA01g01690 | A01 | 750818 | G | A | intron_variant | MODIFIER | c.876+243C>T| |
S112 |
| 3 | BAA01g01690 | A01 | 751552 | G | T | missense_variant | MODERATE | c.385C>A|p.Arg129Ser |
S15 S156 S2 S3 S4 S6 |
| 4 | BAA01g01690 | A01 | 751859 | C | T | synonymous_variant | LOW | c.78G>A|p.Thr26Thr |
S65 |
| 5 | BAA01g01690 | A01 | 753581 | G | A | upstream_gene_variant | MODIFIER | c.-1645C>T| |
S5 |
| 6 | BAA01g01690 | A01 | 755099 | C | T | upstream_gene_variant | MODIFIER | c.-3163G>A| |
S134 |