| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g00960 | A10 | 456700 | G | A | upstream_gene_variant | MODIFIER | c.-2604G>A| |
S153 S213 |
| 2 | BAA10g00960 | A10 | 460830 | C | T | downstream_gene_variant | MODIFIER | c.*114C>T| |
S15 S156 S3 S34 |
| 3 | BAA10g00960 | A10 | 461867 | G | A | downstream_gene_variant | MODIFIER | c.*1151G>A| |
S67 |
| 4 | BAA10g00960 | A10 | 462416 | C | T | downstream_gene_variant | MODIFIER | c.*1700C>T| |
S98 |
| 5 | BAA10g00960 | A10 | 462827 | G | A | downstream_gene_variant | MODIFIER | c.*2111G>A| |
S129 |
| 6 | BAA10g00960 | A10 | 463759 | C | T | downstream_gene_variant | MODIFIER | c.*3043C>T| |
S135 |
| 7 | BAA10g00960 | A10 | 464270 | G | A | downstream_gene_variant | MODIFIER | c.*3554G>A| |
S59 |
| 8 | BAA10g00960 | A10 | 464582 | C | T | downstream_gene_variant | MODIFIER | c.*3866C>T| |
S294 |
| 9 | BAA10g00960 | A10 | 464717 | C | T | downstream_gene_variant | MODIFIER | c.*4001C>T| |
S139 |
| 10 | BAA10g00960 | A10 | 464721 | G | A | downstream_gene_variant | MODIFIER | c.*4005G>A| |
S153 S213 |