| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g01070 | A05 | 618299 | G | A | upstream_gene_variant | MODIFIER | c.-963G>A| |
S192 |
| 2 | BAA05g01070 | A05 | 618956 | G | A | upstream_gene_variant | MODIFIER | c.-306G>A| |
S150 |
| 3 | BAA05g01070 | A05 | 620022 | C | T | missense_variant | MODERATE | c.388C>T|p.Pro130Ser |
S37 |
| 4 | BAA05g01070 | A05 | 620489 | G | A | intron_variant | MODIFIER | c.475-92G>A| |
S293 |
| 5 | BAA05g01070 | A05 | 620962 | G | A | missense_variant | MODERATE | c.856G>A|p.Val286Met |
S69 |
| 6 | BAA05g01070 | A05 | 621108 | G | A | missense_variant | MODERATE | c.1002G>A|p.Met334Ile |
S219 |
| 7 | BAA05g01070 | A05 | 622437 | G | A | downstream_gene_variant | MODIFIER | c.*1251G>A| |
S143 |
| 8 | BAA05g01070 | A05 | 622952 | C | T | downstream_gene_variant | MODIFIER | c.*1766C>T| |
S281 S282 |
| 9 | BAA05g01070 | A05 | 623036 | C | T | downstream_gene_variant | MODIFIER | c.*1850C>T| |
S15 S3 |
| 10 | BAA05g01070 | A05 | 623132 | G | A | downstream_gene_variant | MODIFIER | c.*1946G>A| |
S143 |