| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g39490 | A09 | 47086602 | C | T | missense_variant | MODERATE | c.1177G>A|p.Ala393Thr |
S124 |
| 2 | BAA09g39490 | A09 | 47087817 | C | T | missense_variant | MODERATE | c.208G>A|p.Val70Ile |
S260 |
| 3 | BAA09g39490 | A09 | 47087901 | G | A | missense_variant | MODERATE | c.124C>T|p.Leu42Phe |
S202 |
| 4 | BAA09g39490 | A09 | 47089259 | G | A | upstream_gene_variant | MODIFIER | c.-1235C>T| |
S170 |
| 5 | BAA09g39490 | A09 | 47090823 | C | T | upstream_gene_variant | MODIFIER | c.-2799G>A| |
S191 |
| 6 | BAA09g39490 | A09 | 47091353 | T | C | upstream_gene_variant | MODIFIER | c.-3329A>G| |
S282 |
| 7 | BAA09g39490 | A09 | 47092933 | G | A | upstream_gene_variant | MODIFIER | c.-4909C>T| |
S236 |