| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 182651 | BAA02g21580 | A02 | 11599271 | G | A | downstream_gene_variant | MODIFIER | c.*2256G>A| |
S169 |
| 182652 | BAA02g21580 | A02 | 11599747 | G | A | downstream_gene_variant | MODIFIER | c.*2732G>A| |
S269 |
| 182653 | BAA02g21580 | A02 | 11600578 | C | T | downstream_gene_variant | MODIFIER | c.*3563C>T| |
S66 |
| 182654 | BAA02g21580 | A02 | 11600910 | C | T | downstream_gene_variant | MODIFIER | c.*3895C>T| |
S2 |
| 182655 | BAA02g21580 | A02 | 11600972 | G | A | downstream_gene_variant | MODIFIER | c.*3957G>A| |
S280 |
| 182656 | BAA02g21580 | A02 | 11600976 | C | T | downstream_gene_variant | MODIFIER | c.*3961C>T| |
S284 |
| 182657 | BAA02g21580 | A02 | 11600989 | G | A | downstream_gene_variant | MODIFIER | c.*3974G>A| |
S74 |
| 182658 | BAA02g21580 | A02 | 11601972 | G | A | downstream_gene_variant | MODIFIER | c.*4957G>A| |
S297 |
| 182659 | BAA02g21590 | A02 | 11602919 | C | T | downstream_gene_variant | MODIFIER | c.*2529G>A| |
S293 |
| 182660 | BAA02g21590 | A02 | 11603025 | C | T | downstream_gene_variant | MODIFIER | c.*2423G>A| |
S218 |
| 182661 | BAA02g21590 | A02 | 11603052 | G | A | downstream_gene_variant | MODIFIER | c.*2396C>T| |
S256 |
| 182662 | BAA02g21590 | A02 | 11603185 | C | T | downstream_gene_variant | MODIFIER | c.*2263G>A| |
S88 |
| 182663 | BAA02g21590 | A02 | 11603967 | C | T | downstream_gene_variant | MODIFIER | c.*1481G>A| |
S136 |
| 182664 | BAA02g21590 | A02 | 11604122 | C | T | downstream_gene_variant | MODIFIER | c.*1326G>A| |
S42 |
| 182665 | BAA02g21590 | A02 | 11604515 | C | T | downstream_gene_variant | MODIFIER | c.*933G>A| |
S216 |
| 182666 | BAA02g21590 | A02 | 11605609 | C | T | missense_variant | MODERATE | c.766G>A|p.Glu256Lys |
S135 |
| 182667 | BAA02g21590 | A02 | 11605710 | C | T | missense_variant | MODERATE | c.665G>A|p.Gly222Glu |
S178 |
| 182668 | BAA02g21590 | A02 | 11605936 | C | T | missense_variant | MODERATE | c.439G>A|p.Glu147Lys |
S305 |
| 182669 | BAA02g21590 | A02 | 11606113 | C | T | missense_variant | MODERATE | c.262G>A|p.Val88Ile |
S38 |
| 182670 | BAA02g21590 | A02 | 11607445 | G | A | upstream_gene_variant | MODIFIER | c.-1071C>T| |
S125 |
| 182671 | BAA02g21590 | A02 | 11607747 | G | A | upstream_gene_variant | MODIFIER | c.-1373C>T| |
S136 |
| 182672 | BAA02g21590 | A02 | 11608182 | C | T | upstream_gene_variant | MODIFIER | c.-1808G>A| |
S104 S52 |
| 182673 | BAA02g21590 | A02 | 11608640 | C | T | upstream_gene_variant | MODIFIER | c.-2266G>A| |
S66 |
| 182674 | BAA02g21590 | A02 | 11608658 | C | T | upstream_gene_variant | MODIFIER | c.-2284G>A| |
S105 S106 |
| 182675 | BAA02g21590 | A02 | 11609023 | C | T | upstream_gene_variant | MODIFIER | c.-2649G>A| |
S221 |