| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 182351 | BAA02g21380-BAA02g21390 | A02 | 11469120 | G | A | intergenic_region | MODIFIER | n.11469120G>A| |
S291 |
| 182352 | BAA02g21380-BAA02g21390 | A02 | 11469140 | G | A | intergenic_region | MODIFIER | n.11469140G>A| |
S10 |
| 182353 | BAA02g21390 | A02 | 11469642 | C | T | upstream_gene_variant | MODIFIER | c.-4730C>T| |
S177 |
| 182354 | BAA02g21390 | A02 | 11472056 | G | A | upstream_gene_variant | MODIFIER | c.-2316G>A| |
S168 |
| 182355 | BAA02g21390 | A02 | 11472078 | G | A | upstream_gene_variant | MODIFIER | c.-2294G>A| |
S168 |
| 182356 | BAA02g21390 | A02 | 11474471 | C | T | missense_variant | MODERATE | c.100C>T|p.His34Tyr |
S138 |
| 182357 | BAA02g21390 | A02 | 11475004 | C | T | synonymous_variant | LOW | c.474C>T|p.Ser158Ser |
S51 |
| 182358 | BAA02g21390 | A02 | 11480149 | C | T | intron_variant | MODIFIER | c.584-228C>T| |
S87 |
| 182359 | BAA02g21390 | A02 | 11485312 | T | G | downstream_gene_variant | MODIFIER | c.*4412T>G| |
S191 |
| 182360 | BAA02g21390 | A02 | 11485432 | G | A | downstream_gene_variant | MODIFIER | c.*4532G>A| |
S231 |
| 182361 | BAA02g21390 | A02 | 11485485 | C | T | downstream_gene_variant | MODIFIER | c.*4585C>T| |
S289 |
| 182362 | BAA02g21400 | A02 | 11489877 | G | A | downstream_gene_variant | MODIFIER | c.*1529C>T| |
S264 |
| 182363 | BAA02g21400 | A02 | 11490248 | G | A | downstream_gene_variant | MODIFIER | c.*1158C>T| |
S159 S243 |
| 182364 | BAA02g21400 | A02 | 11490459 | C | T | downstream_gene_variant | MODIFIER | c.*947G>A| |
S108 |
| 182365 | BAA02g21400 | A02 | 11491022 | G | A | downstream_gene_variant | MODIFIER | c.*384C>T| |
S286 |
| 182366 | BAA02g21400 | A02 | 11491108 | C | T | downstream_gene_variant | MODIFIER | c.*298G>A| |
S6 |
| 182367 | BAA02g21400 | A02 | 11491608 | C | T | missense_variant | MODERATE | c.1721G>A|p.Cys574Tyr |
S115 |
| 182368 | BAA02g21400 | A02 | 11492269 | C | T | missense_variant | MODERATE | c.1228G>A|p.Gly410Arg |
S124 |
| 182369 | BAA02g21400 | A02 | 11493664 | G | A | missense_variant | MODERATE | c.289C>T|p.Leu97Phe |
S116 |
| 182370 | BAA02g21400 | A02 | 11494150 | G | A | upstream_gene_variant | MODIFIER | c.-198C>T| |
S161 |
| 182371 | BAA02g21400 | A02 | 11495067 | G | A | upstream_gene_variant | MODIFIER | c.-1115C>T| |
S306 S308 |
| 182372 | BAA02g21400 | A02 | 11497220 | C | T | upstream_gene_variant | MODIFIER | c.-3268G>A| |
S202 |
| 182373 | BAA02g21400 | A02 | 11497494 | G | A | upstream_gene_variant | MODIFIER | c.-3542C>T| |
S69 |
| 182374 | BAA02g21400 | A02 | 11498328 | C | T | upstream_gene_variant | MODIFIER | c.-4376G>A| |
S163 |
| 182375 | BAA02g21410 | A02 | 11499117 | C | T | downstream_gene_variant | MODIFIER | c.*218C>T| |
S53 |