| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 156451 | BAA02g04450 | A02 | 1933631 | C | T | upstream_gene_variant | MODIFIER | c.-1291G>A| |
S159 S187 S188 S243 S276 S299 |
| 156452 | BAA02g04460 | A02 | 1933901 | C | T | missense_variant | MODERATE | c.452G>A|p.Arg151Lys |
S19 |
| 156453 | BAA02g04460 | A02 | 1934214 | G | A | missense_variant | MODERATE | c.139C>T|p.Pro47Ser |
S96 |
| 156454 | BAA02g04460 | A02 | 1937745 | C | T | upstream_gene_variant | MODIFIER | c.-3393G>A| |
S272 |
| 156455 | BAA02g04480 | A02 | 1938044 | C | T | missense_variant&splice_region_variant | MODERATE | c.1924G>A|p.Glu642Lys |
S112 |
| 156456 | BAA02g04460 | A02 | 1938590 | C | T | upstream_gene_variant | MODIFIER | c.-4238G>A| |
S58 |
| 156457 | BAA02g04480 | A02 | 1938861 | G | A | missense_variant | MODERATE | c.1567C>T|p.Pro523Ser |
S286 |
| 156458 | BAA02g04480 | A02 | 1939074 | C | T | missense_variant | MODERATE | c.1354G>A|p.Ala452Thr |
S242 |
| 156459 | BAA02g04470 | A02 | 1939507 | G | A | upstream_gene_variant | MODIFIER | c.-3703C>T| |
S81 |
| 156460 | BAA02g04480 | A02 | 1939637 | G | A | synonymous_variant | LOW | c.912C>T|p.Leu304Leu |
S44 |
| 156461 | BAA02g04470 | A02 | 1940563 | C | T | upstream_gene_variant | MODIFIER | c.-4759G>A| |
S85 |
| 156462 | BAA02g04470 | A02 | 1940642 | C | T | upstream_gene_variant | MODIFIER | c.-4838G>A| |
S6 |
| 156463 | BAA02g04480 | A02 | 1941059 | G | A | missense_variant | MODERATE | c.121C>T|p.Pro41Ser |
S223 |
| 156464 | BAA02g04480 | A02 | 1941456 | C | T | upstream_gene_variant | MODIFIER | c.-277G>A| |
S76 |
| 156465 | BAA02g04480 | A02 | 1941576 | C | T | upstream_gene_variant | MODIFIER | c.-397G>A| |
S180 |
| 156466 | BAA02g04480 | A02 | 1941904 | G | A | upstream_gene_variant | MODIFIER | c.-725C>T| |
S84 S93 |
| 156467 | BAA02g04480 | A02 | 1942134 | G | A | upstream_gene_variant | MODIFIER | c.-955C>T| |
S197 |
| 156468 | BAA02g04480 | A02 | 1942458 | G | A | upstream_gene_variant | MODIFIER | c.-1279C>T| |
S45 |
| 156469 | BAA02g04480 | A02 | 1942674 | G | A | upstream_gene_variant | MODIFIER | c.-1495C>T| |
S155 S211 |
| 156470 | BAA02g04480 | A02 | 1943231 | C | T | upstream_gene_variant | MODIFIER | c.-2052G>A| |
S42 |
| 156471 | BAA02g04490 | A02 | 1943671 | G | A | missense_variant | MODERATE | c.295G>A|p.Ala99Thr |
S17 |
| 156472 | BAA02g04490 | A02 | 1943811 | G | A | synonymous_variant | LOW | c.435G>A|p.Glu145Glu |
S259 |
| 156473 | BAA02g04490 | A02 | 1943859 | C | T | synonymous_variant | LOW | c.483C>T|p.Thr161Thr |
S88 |
| 156474 | BAA02g04480 | A02 | 1945450 | G | A | upstream_gene_variant | MODIFIER | c.-4271C>T| |
S79 S91 |
| 156475 | BAA02g04490 | A02 | 1948952 | C | T | downstream_gene_variant | MODIFIER | c.*4724C>T| |
S131 |