| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g09830 | A01 | 4399240 | C | T | upstream_gene_variant | MODIFIER | c.-4950C>T| |
S79 S84 |
| 2 | BAA01g09830 | A01 | 4399392 | C | T | upstream_gene_variant | MODIFIER | c.-4798C>T| |
S203 |
| 3 | BAA01g09830 | A01 | 4400038 | C | T | upstream_gene_variant | MODIFIER | c.-4152C>T| |
S99 |
| 4 | BAA01g09830 | A01 | 4401324 | G | A | upstream_gene_variant | MODIFIER | c.-2866G>A| |
S281 |
| 5 | BAA01g09830 | A01 | 4403458 | G | A | upstream_gene_variant | MODIFIER | c.-732G>A| |
S237 |
| 6 | BAA01g09830 | A01 | 4403490 | G | A | upstream_gene_variant | MODIFIER | c.-700G>A| |
S161 |
| 7 | BAA01g09830 | A01 | 4404215 | G | A | missense_variant | MODERATE | c.26G>A|p.Arg9Lys |
S271 |
| 8 | BAA01g09830 | A01 | 4404538 | G | A | intron_variant | MODIFIER | c.211+138G>A| |
S138 |
| 9 | BAA01g09830 | A01 | 4404563 | C | T | intron_variant | MODIFIER | c.211+163C>T| |
S210 S225 |
| 10 | BAA01g09830 | A01 | 4404588 | G | A | intron_variant | MODIFIER | c.211+188G>A| |
S74 |
| 11 | BAA01g09830 | A01 | 4405324 | G | A | intron_variant | MODIFIER | c.212-695G>A| |
S87 |
| 12 | BAA01g09830 | A01 | 4405336 | G | A | intron_variant | MODIFIER | c.212-683G>A| |
S274 |
| 13 | BAA01g09830 | A01 | 4407922 | G | A | downstream_gene_variant | MODIFIER | c.*413G>A| |
S204 |
| 14 | BAA01g09830 | A01 | 4408375 | C | T | downstream_gene_variant | MODIFIER | c.*866C>T| |
S246 |
| 15 | BAA01g09830 | A01 | 4410511 | C | T | downstream_gene_variant | MODIFIER | c.*3002C>T| |
S278 |
| 16 | BAA01g09830 | A01 | 4410566 | G | A | downstream_gene_variant | MODIFIER | c.*3057G>A| |
S289 S290 |
| 17 | BAA01g09830 | A01 | 4410777 | G | A | downstream_gene_variant | MODIFIER | c.*3268G>A| |
S229 |