| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 217651 | BAA02g32680 | A02 | 27903711 | C | T | downstream_gene_variant | MODIFIER | c.*3795G>A| |
S284 |
| 217652 | BAA02g32680 | A02 | 27903737 | C | T | downstream_gene_variant | MODIFIER | c.*3769G>A| |
S130 |
| 217653 | BAA02g32680 | A02 | 27904543 | G | A | downstream_gene_variant | MODIFIER | c.*2963C>T| |
S298 |
| 217654 | BAA02g32680 | A02 | 27904650 | C | T | downstream_gene_variant | MODIFIER | c.*2856G>A| |
S202 |
| 217655 | BAA02g32680 | A02 | 27904949 | C | T | downstream_gene_variant | MODIFIER | c.*2557G>A| |
S51 |
| 217656 | BAA02g32680 | A02 | 27905216 | C | T | downstream_gene_variant | MODIFIER | c.*2290G>A| |
S87 |
| 217657 | BAA02g32680 | A02 | 27905304 | G | A | downstream_gene_variant | MODIFIER | c.*2202C>T| |
S223 |
| 217658 | BAA02g32680 | A02 | 27906027 | G | A | downstream_gene_variant | MODIFIER | c.*1479C>T| |
S185 S95 |
| 217659 | BAA02g32680 | A02 | 27906068 | G | A | downstream_gene_variant | MODIFIER | c.*1438C>T| |
S176 |
| 217660 | BAA02g32680 | A02 | 27906440 | C | T | downstream_gene_variant | MODIFIER | c.*1066G>A| |
S241 |
| 217661 | BAA02g32680 | A02 | 27909981 | G | A | upstream_gene_variant | MODIFIER | c.-1884C>T| |
S306 |
| 217662 | BAA02g32680 | A02 | 27911490 | C | T | upstream_gene_variant | MODIFIER | c.-3393G>A| |
S292 |
| 217663 | BAA02g32680 | A02 | 27911625 | G | A | upstream_gene_variant | MODIFIER | c.-3528C>T| |
S224 |
| 217664 | BAA02g32680 | A02 | 27911993 | G | A | upstream_gene_variant | MODIFIER | c.-3896C>T| |
S38 |
| 217665 | BAA02g32680 | A02 | 27912248 | G | A | upstream_gene_variant | MODIFIER | c.-4151C>T| |
S146 |
| 217666 | BAA02g32680 | A02 | 27912691 | C | T | upstream_gene_variant | MODIFIER | c.-4594G>A| |
S15 |
| 217667 | BAA02g32680 | A02 | 27912767 | C | T | upstream_gene_variant | MODIFIER | c.-4670G>A| |
S167 |
| 217668 | BAA02g32690 | A02 | 27913784 | C | T | missense_variant | MODERATE | c.403C>T|p.His135Tyr |
S299 |
| 217669 | BAA02g32690 | A02 | 27914552 | G | A | synonymous_variant | LOW | c.1044G>A|p.Gln348Gln |
S12 |
| 217670 | BAA02g32690 | A02 | 27914853 | C | T | missense_variant | MODERATE | c.1256C>T|p.Ser419Phe |
S301 S304 |
| 217671 | BAA02g32690 | A02 | 27915429 | G | A | missense_variant | MODERATE | c.1585G>A|p.Asp529Asn |
S256 |
| 217672 | BAA02g32690 | A02 | 27915678 | C | T | missense_variant | MODERATE | c.1834C>T|p.Arg612Trp |
S123 |
| 217673 | BAA02g32700 | A02 | 27928676 | G | A | upstream_gene_variant | MODIFIER | c.-3008G>A| |
S47 |
| 217674 | BAA02g32700 | A02 | 27930396 | C | T | upstream_gene_variant | MODIFIER | c.-1288C>T| |
S6 |
| 217675 | BAA02g32700 | A02 | 27930479 | C | T | upstream_gene_variant | MODIFIER | c.-1205C>T| |
S172 S217 |