| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 168451 | BAA02g13750 | A02 | 6410436 | C | T | missense_variant | MODERATE | c.242C>T|p.Ser81Phe |
S112 |
| 168452 | BAA02g13750 | A02 | 6411174 | C | T | downstream_gene_variant | MODIFIER | c.*265C>T| |
S272 |
| 168453 | BAA02g13750 | A02 | 6411936 | G | A | downstream_gene_variant | MODIFIER | c.*1027G>A| |
S64 |
| 168454 | BAA02g13750 | A02 | 6411942 | G | A | downstream_gene_variant | MODIFIER | c.*1033G>A| |
S188 |
| 168455 | BAA02g13750 | A02 | 6412220 | C | T | downstream_gene_variant | MODIFIER | c.*1311C>T| |
S181 |
| 168456 | BAA02g13750 | A02 | 6412367 | C | T | downstream_gene_variant | MODIFIER | c.*1458C>T| |
S124 |
| 168457 | BAA02g13750 | A02 | 6412965 | G | A | downstream_gene_variant | MODIFIER | c.*2056G>A| |
S148 S30 S31 |
| 168458 | BAA02g13760 | A02 | 6413912 | C | T | upstream_gene_variant | MODIFIER | c.-158G>A| |
S112 |
| 168459 | BAA02g13760 | A02 | 6414457 | G | A | upstream_gene_variant | MODIFIER | c.-703C>T| |
S286 |
| 168460 | BAA02g13770 | A02 | 6419214 | G | A | missense_variant | MODERATE | c.572C>T|p.Ala191Val |
S36 |
| 168461 | BAA02g13770 | A02 | 6419333 | G | A | intron_variant | MODIFIER | c.525+12C>T| |
S203 |
| 168462 | BAA02g13770 | A02 | 6419612 | G | A | intron_variant | MODIFIER | c.268-10C>T| |
S144 |
| 168463 | BAA02g13770 | A02 | 6420276 | C | T | upstream_gene_variant | MODIFIER | c.-194G>A| |
S182 |
| 168464 | BAA02g13770 | A02 | 6422579 | G | A | upstream_gene_variant | MODIFIER | c.-2497C>T| |
S302 |
| 168465 | BAA02g13770 | A02 | 6422615 | G | A | upstream_gene_variant | MODIFIER | c.-2533C>T| |
S203 |
| 168466 | BAA02g13770 | A02 | 6423495 | C | T | upstream_gene_variant | MODIFIER | c.-3413G>A| |
S120 |
| 168467 | BAA02g13770 | A02 | 6423567 | G | A | upstream_gene_variant | MODIFIER | c.-3485C>T| |
S256 |
| 168468 | BAA02g13770 | A02 | 6424639 | C | T | upstream_gene_variant | MODIFIER | c.-4557G>A| |
S13 |
| 168469 | BAA02g13770-BAA02g13780 | A02 | 6427723 | C | T | intergenic_region | MODIFIER | n.6427723C>T| |
S128 |
| 168470 | BAA02g13780 | A02 | 6431466 | C | T | downstream_gene_variant | MODIFIER | c.*1634G>A| |
S219 S72 |
| 168471 | BAA02g13780 | A02 | 6431479 | G | A | downstream_gene_variant | MODIFIER | c.*1621C>T| |
S111 |
| 168472 | BAA02g13780 | A02 | 6431780 | C | G | downstream_gene_variant | MODIFIER | c.*1320G>C| |
S249 |
| 168473 | BAA02g13780 | A02 | 6432688 | C | T | downstream_gene_variant | MODIFIER | c.*412G>A| |
S115 |
| 168474 | BAA02g13780 | A02 | 6432861 | C | T | downstream_gene_variant | MODIFIER | c.*239G>A| |
S103 |
| 168475 | BAA02g13780 | A02 | 6433276 | G | A | missense_variant | MODERATE | c.130C>T|p.Pro44Ser |
S125 |