| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 165351 | BAA02g11560 | A02 | 5230901 | G | A | upstream_gene_variant | MODIFIER | c.-863G>A| |
S279 |
| 165352 | BAA02g11560 | A02 | 5232328 | G | A | missense_variant | MODERATE | c.350G>A|p.Arg117Lys |
S20 |
| 165353 | BAA02g11570 | A02 | 5234317 | G | A | splice_region_variant&intron_variant | LOW | c.66-6G>A| |
S107 |
| 165354 | BAA02g11580 | A02 | 5234719 | G | A | upstream_gene_variant | MODIFIER | c.-1441G>A| |
S169 |
| 165355 | BAA02g11570 | A02 | 5235680 | C | T | synonymous_variant | LOW | c.564C>T|p.Val188Val |
S38 |
| 165356 | BAA02g11580 | A02 | 5236455 | C | T | missense_variant | MODERATE | c.296C>T|p.Ser99Leu |
S286 |
| 165357 | BAA02g11590 | A02 | 5239969 | G | A | upstream_gene_variant | MODIFIER | c.-1259G>A| |
S261 |
| 165358 | BAA02g11580 | A02 | 5241304 | G | A | downstream_gene_variant | MODIFIER | c.*4719G>A| |
S237 |
| 165359 | BAA02g11590 | A02 | 5241405 | G | A | missense_variant | MODERATE | c.88G>A|p.Glu30Lys |
S113 |
| 165360 | BAA02g11590 | A02 | 5241680 | G | A | synonymous_variant | LOW | c.363G>A|p.Thr121Thr |
S136 |
| 165361 | BAA02g11590 | A02 | 5241732 | G | A | missense_variant | MODERATE | c.415G>A|p.Ala139Thr |
S269 |
| 165362 | BAA02g11610 | A02 | 5243174 | A | T | upstream_gene_variant | MODIFIER | c.-4324A>T| |
S11 |
| 165363 | BAA02g11610 | A02 | 5244052 | C | T | upstream_gene_variant | MODIFIER | c.-3446C>T| |
S257 |
| 165364 | BAA02g11600 | A02 | 5245042 | C | T | missense_variant | MODERATE | c.1018G>A|p.Asp340Asn |
S3 |
| 165365 | BAA02g11610 | A02 | 5245225 | G | A | upstream_gene_variant | MODIFIER | c.-2273G>A| |
S125 |
| 165366 | BAA02g11610 | A02 | 5245273 | C | T | upstream_gene_variant | MODIFIER | c.-2225C>T| |
S240 |
| 165367 | BAA02g11600 | A02 | 5245448 | C | T | stop_gained | HIGH | c.929G>A|p.Trp310* |
S200 |
| 165368 | BAA02g11600 | A02 | 5246163 | C | T | missense_variant | MODERATE | c.502G>A|p.Asp168Asn |
S115 |
| 165369 | BAA02g11600 | A02 | 5246792 | G | A | missense_variant | MODERATE | c.35C>T|p.Pro12Leu |
S177 |
| 165370 | BAA02g11600 | A02 | 5246878 | C | T | upstream_gene_variant | MODIFIER | c.-52G>A| |
S124 |
| 165371 | BAA02g11610 | A02 | 5248441 | G | A | synonymous_variant | LOW | c.510G>A|p.Lys170Lys |
S9 |
| 165372 | BAA02g11600 | A02 | 5248953 | C | T | upstream_gene_variant | MODIFIER | c.-2127G>A| |
S195 |
| 165373 | BAA02g11600 | A02 | 5250263 | C | T | upstream_gene_variant | MODIFIER | c.-3437G>A| |
S138 |
| 165374 | BAA02g11600 | A02 | 5250594 | G | A | upstream_gene_variant | MODIFIER | c.-3768C>T| |
S236 |
| 165375 | BAA02g11620 | A02 | 5252269 | C | T | upstream_gene_variant | MODIFIER | c.-1394C>T| |
S283 |