| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 153501 | BAA02g01960 | A02 | 880120 | C | T | upstream_gene_variant | MODIFIER | c.-157C>T| |
S110 |
| 153502 | BAA02g01970 | A02 | 881321 | G | A | upstream_gene_variant | MODIFIER | c.-547G>A| |
S237 |
| 153503 | BAA02g01970 | A02 | 881332 | C | T | upstream_gene_variant | MODIFIER | c.-536C>T| |
S178 |
| 153504 | BAA02g01970 | A02 | 881413 | C | T | upstream_gene_variant | MODIFIER | c.-455C>T| |
S216 |
| 153505 | BAA02g01970 | A02 | 881465 | C | T | upstream_gene_variant | MODIFIER | c.-403C>T| |
S34 |
| 153506 | BAA02g01970 | A02 | 881502 | C | T | upstream_gene_variant | MODIFIER | c.-366C>T| |
S195 |
| 153507 | BAA02g01970 | A02 | 881830 | G | A | upstream_gene_variant | MODIFIER | c.-38G>A| |
S208 |
| 153508 | BAA02g01980 | A02 | 882597 | G | A | upstream_gene_variant | MODIFIER | c.-2987G>A| |
S187 S298 |
| 153509 | BAA02g01970 | A02 | 882728 | C | T | missense_variant | MODERATE | c.421C>T|p.Pro141Ser |
S274 |
| 153510 | BAA02g01970 | A02 | 883704 | G | A | missense_variant | MODERATE | c.827G>A|p.Ser276Asn |
S48 |
| 153511 | BAA02g01980 | A02 | 884035 | G | A | upstream_gene_variant | MODIFIER | c.-1549G>A| |
S146 |
| 153512 | BAA02g01980 | A02 | 886222 | G | A | missense_variant | MODERATE | c.476G>A|p.Ser159Asn |
S25 |
| 153513 | BAA02g01970 | A02 | 887136 | G | A | downstream_gene_variant | MODIFIER | c.*3246G>A| |
S256 |
| 153514 | BAA02g01970 | A02 | 888124 | G | A | downstream_gene_variant | MODIFIER | c.*4234G>A| |
S23 |
| 153515 | BAA02g01990 | A02 | 889675 | C | T | upstream_gene_variant | MODIFIER | c.-372G>A| |
S283 |
| 153516 | BAA02g02000 | A02 | 890123 | G | A | missense_variant | MODERATE | c.305C>T|p.Ser102Phe |
S4 |
| 153517 | BAA02g01990 | A02 | 890359 | G | A | upstream_gene_variant | MODIFIER | c.-1056C>T| |
S268 |
| 153518 | BAA02g01990 | A02 | 891466 | G | A | upstream_gene_variant | MODIFIER | c.-2163C>T| |
S57 |
| 153519 | BAA02g01990 | A02 | 891781 | C | T | upstream_gene_variant | MODIFIER | c.-2478G>A| |
S142 |
| 153520 | BAA02g01990 | A02 | 891897 | G | A | upstream_gene_variant | MODIFIER | c.-2594C>T| |
S293 |
| 153521 | BAA02g01990 | A02 | 892073 | G | A | upstream_gene_variant | MODIFIER | c.-2770C>T| |
S188 |
| 153522 | BAA02g02010 | A02 | 894104 | G | A | missense_variant | MODERATE | c.1412C>T|p.Ala471Val |
S45 |
| 153523 | BAA02g02000 | A02 | 894452 | G | A | upstream_gene_variant | MODIFIER | c.-3298C>T| |
S294 |
| 153524 | BAA02g02010 | A02 | 894694 | C | T | stop_gained | HIGH | c.1101G>A|p.Trp367* |
S196 |
| 153525 | BAA02g02010 | A02 | 894726 | G | A | missense_variant | MODERATE | c.1069C>T|p.His357Tyr |
S294 |