| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g39690 | A01 | 26352560 | C | T | missense_variant | MODERATE | c.814G>A|p.Val272Ile |
S50 |
| 2 | BAA01g39690 | A01 | 26353683 | G | A | synonymous_variant | LOW | c.81C>T|p.Val27Val |
S294 |
| 3 | BAA01g39690 | A01 | 26353729 | C | T | missense_variant | MODERATE | c.35G>A|p.Ser12Asn |
S176 |
| 4 | BAA01g39690 | A01 | 26353944 | C | T | upstream_gene_variant | MODIFIER | c.-181G>A| |
S289 S290 |
| 5 | BAA01g39690 | A01 | 26354068 | G | A | upstream_gene_variant | MODIFIER | c.-305C>T| |
S252 |
| 6 | BAA01g39690 | A01 | 26354743 | G | A | upstream_gene_variant | MODIFIER | c.-980C>T| |
S246 |
| 7 | BAA01g39690 | A01 | 26355998 | G | A | upstream_gene_variant | MODIFIER | c.-2235C>T| |
S116 |
| 8 | BAA01g39690 | A01 | 26356562 | C | T | upstream_gene_variant | MODIFIER | c.-2799G>A| |
S177 |
| 9 | BAA01g39690 | A01 | 26357135 | C | T | upstream_gene_variant | MODIFIER | c.-3372G>A| |
S39 |
| 10 | BAA01g39690 | A01 | 26358197 | G | A | upstream_gene_variant | MODIFIER | c.-4434C>T| |
S173 |
| 11 | BAA01g39690 | A01 | 26358521 | C | T | upstream_gene_variant | MODIFIER | c.-4758G>A| |
S235 |
| 12 | BAA01g39690 | A01 | 26358739 | C | T | upstream_gene_variant | MODIFIER | c.-4976G>A| |
S183 S198 |