| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 83501 | BAA01g44260-BAA01g44270 | A01 | 29420192 | G | A | intergenic_region | MODIFIER | n.29420192G>A| |
S152 |
| 83502 | BAA01g44260-BAA01g44270 | A01 | 29420995 | G | A | intergenic_region | MODIFIER | n.29420995G>A| |
S105 S106 |
| 83503 | BAA01g44260-BAA01g44270 | A01 | 29423055 | G | A | intergenic_region | MODIFIER | n.29423055G>A| |
S208 |
| 83504 | BAA01g44270 | A01 | 29424184 | C | T | downstream_gene_variant | MODIFIER | c.*4960G>A| |
S15 S199 S205 S208 S209 S231 S239 S286 S296 S30 S60 S64 |
| 83505 | BAA01g44270 | A01 | 29425597 | C | T | downstream_gene_variant | MODIFIER | c.*3547G>A| |
S32 |
| 83506 | BAA01g44270 | A01 | 29425696 | A | C | downstream_gene_variant | MODIFIER | c.*3448T>G| |
S256 |
| 83507 | BAA01g44270 | A01 | 29426549 | C | T | downstream_gene_variant | MODIFIER | c.*2595G>A| |
S303 |
| 83508 | BAA01g44270 | A01 | 29426588 | C | T | downstream_gene_variant | MODIFIER | c.*2556G>A| |
S270 |
| 83509 | BAA01g44270 | A01 | 29426763 | A | G | downstream_gene_variant | MODIFIER | c.*2381T>C| |
S123 |
| 83510 | BAA01g44270 | A01 | 29426800 | G | A | downstream_gene_variant | MODIFIER | c.*2344C>T| |
S217 |
| 83511 | BAA01g44270 | A01 | 29428623 | C | T | downstream_gene_variant | MODIFIER | c.*521G>A| |
S241 |
| 83512 | BAA01g44270 | A01 | 29428716 | C | T | downstream_gene_variant | MODIFIER | c.*428G>A| |
S153 S213 |
| 83513 | BAA01g44270 | A01 | 29429302 | C | T | missense_variant | MODERATE | c.889G>A|p.Ala297Thr |
S279 |
| 83514 | BAA01g44270 | A01 | 29429602 | G | A | missense_variant | MODERATE | c.589C>T|p.Leu197Phe |
S95 |
| 83515 | BAA01g44270 | A01 | 29430504 | C | T | upstream_gene_variant | MODIFIER | c.-314G>A| |
S134 |
| 83516 | BAA01g44270 | A01 | 29430856 | C | T | upstream_gene_variant | MODIFIER | c.-666G>A| |
S178 |
| 83517 | BAA01g44270 | A01 | 29433443 | G | A | upstream_gene_variant | MODIFIER | c.-3253C>T| |
S176 |
| 83518 | BAA01g44280 | A01 | 29437291 | C | T | missense_variant | MODERATE | c.700C>T|p.Leu234Phe |
S88 |
| 83519 | BAA01g44280 | A01 | 29437677 | C | T | synonymous_variant | LOW | c.999C>T|p.Ile333Ile |
S11 |
| 83520 | BAA01g44280 | A01 | 29438560 | C | T | synonymous_variant | LOW | c.1590C>T|p.Phe530Phe |
S125 |
| 83521 | BAA01g44290 | A01 | 29441371 | C | T | upstream_gene_variant | MODIFIER | c.-2307C>T| |
S19 |
| 83522 | BAA01g44290 | A01 | 29442775 | G | A | upstream_gene_variant | MODIFIER | c.-903G>A| |
S202 |
| 83523 | BAA01g44290 | A01 | 29442926 | C | T | upstream_gene_variant | MODIFIER | c.-752C>T| |
S177 |
| 83524 | BAA01g44290 | A01 | 29443294 | C | T | upstream_gene_variant | MODIFIER | c.-384C>T| |
S153 S213 |
| 83525 | BAA01g44290 | A01 | 29443639 | C | T | upstream_gene_variant | MODIFIER | c.-39C>T| |
S168 |