| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA03g41820 | A03 | 19701728 | C | T | downstream_gene_variant | MODIFIER | c.*2112G>A| |
S96 |
| 2 | BAA03g41820 | A03 | 19702061 | C | T | downstream_gene_variant | MODIFIER | c.*1779G>A| |
S279 |
| 3 | BAA03g41820 | A03 | 19702241 | C | T | downstream_gene_variant | MODIFIER | c.*1599G>A| |
S15 |
| 4 | BAA03g41820 | A03 | 19702757 | G | A | downstream_gene_variant | MODIFIER | c.*1083C>T| |
S155 |
| 5 | BAA03g41820 | A03 | 19703236 | G | A | downstream_gene_variant | MODIFIER | c.*604C>T| |
S105 S106 |
| 6 | BAA03g41820 | A03 | 19703848 | C | T | missense_variant | MODERATE | c.754G>A|p.Asp252Asn |
S158 |
| 7 | BAA03g41820 | A03 | 19704173 | G | A | missense_variant | MODERATE | c.688C>T|p.His230Tyr |
S164 |
| 8 | BAA03g41820 | A03 | 19704656 | C | T | synonymous_variant | LOW | c.267G>A|p.Leu89Leu |
S293 |
| 9 | BAA03g41820 | A03 | 19704788 | C | T | intron_variant | MODIFIER | c.163-28G>A| |
S42 S8 |
| 10 | BAA03g41820 | A03 | 19705308 | C | T | upstream_gene_variant | MODIFIER | c.-317G>A| |
S208 S93 |
| 11 | BAA03g41820 | A03 | 19706022 | C | T | upstream_gene_variant | MODIFIER | c.-1031G>A| |
S221 |
| 12 | BAA03g41820 | A03 | 19707202 | G | A | upstream_gene_variant | MODIFIER | c.-2211C>T| |
S259 |
| 13 | BAA03g41820 | A03 | 19707821 | G | A | upstream_gene_variant | MODIFIER | c.-2830C>T| |
S109 |
| 14 | BAA03g41820 | A03 | 19707847 | G | A | upstream_gene_variant | MODIFIER | c.-2856C>T| |
S50 |
| 15 | BAA03g41820 | A03 | 19708056 | C | T | upstream_gene_variant | MODIFIER | c.-3065G>A| |
S157 S163 |
| 16 | BAA03g41820 | A03 | 19708289 | G | A | upstream_gene_variant | MODIFIER | c.-3298C>T| |
S226 |
| 17 | BAA03g41820 | A03 | 19708840 | G | A | upstream_gene_variant | MODIFIER | c.-3849C>T| |
S233 |