| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 17451 | BAA01g13120 | A01 | 6228417 | C | T | upstream_gene_variant | MODIFIER | c.-588C>T| |
S167 |
| 17452 | BAA01g13120 | A01 | 6228445 | C | T | upstream_gene_variant | MODIFIER | c.-560C>T| |
S255 |
| 17453 | BAA01g13120 | A01 | 6228860 | C | T | upstream_gene_variant | MODIFIER | c.-145C>T| |
S305 |
| 17454 | BAA01g13120 | A01 | 6229271 | G | A | synonymous_variant | LOW | c.267G>A|p.Leu89Leu |
S34 |
| 17455 | BAA01g13120 | A01 | 6230378 | C | T | synonymous_variant | LOW | c.1374C>T|p.Ile458Ile |
S153 |
| 17456 | BAA01g13120 | A01 | 6230534 | G | A | synonymous_variant | LOW | c.1530G>A|p.Gln510Gln |
S168 |
| 17457 | BAA01g13120 | A01 | 6230573 | G | A | synonymous_variant | LOW | c.1569G>A|p.Gln523Gln |
S156 |
| 17458 | BAA01g13120 | A01 | 6230896 | G | A | missense_variant | MODERATE | c.1892G>A|p.Gly631Glu |
S256 |
| 17459 | BAA01g13130 | A01 | 6231703 | G | A | synonymous_variant | LOW | c.420C>T|p.Leu140Leu |
S297 |
| 17460 | BAA01g13130 | A01 | 6233929 | C | T | upstream_gene_variant | MODIFIER | c.-1640G>A| |
S230 |
| 17461 | BAA01g13140 | A01 | 6234391 | G | A | missense_variant | MODERATE | c.371G>A|p.Gly124Glu |
S306 S308 |
| 17462 | BAA01g13140 | A01 | 6234627 | C | T | missense_variant | MODERATE | c.607C>T|p.Leu203Phe |
S269 |
| 17463 | BAA01g13140 | A01 | 6235740 | G | A | synonymous_variant | LOW | c.1251G>A|p.Gln417Gln |
S180 |
| 17464 | BAA01g13140 | A01 | 6235795 | G | A | missense_variant | MODERATE | c.1306G>A|p.Glu436Lys |
S224 |
| 17465 | BAA01g13150 | A01 | 6238945 | G | A | synonymous_variant | LOW | c.270G>A|p.Pro90Pro |
S306 |
| 17466 | BAA01g13140 | A01 | 6240048 | C | T | downstream_gene_variant | MODIFIER | c.*4230C>T| |
S61 |
| 17467 | BAA01g13150 | A01 | 6240135 | C | T | missense_variant | MODERATE | c.799C>T|p.Leu267Phe |
S200 |
| 17468 | BAA01g13150 | A01 | 6241352 | G | A | downstream_gene_variant | MODIFIER | c.*1140G>A| |
S271 |
| 17469 | BAA01g13150 | A01 | 6241770 | C | T | downstream_gene_variant | MODIFIER | c.*1558C>T| |
S78 S83 |
| 17470 | BAA01g13150 | A01 | 6241828 | G | A | downstream_gene_variant | MODIFIER | c.*1616G>A| |
S109 |
| 17471 | BAA01g13160 | A01 | 6242432 | G | A | missense_variant | MODERATE | c.779C>T|p.Ser260Leu |
S257 |
| 17472 | BAA01g13160 | A01 | 6242801 | A | C | missense_variant | MODERATE | c.410T>G|p.Val137Gly |
S165 S195 S47 S95 |
| 17473 | BAA01g13160 | A01 | 6242980 | G | A | synonymous_variant | LOW | c.231C>T|p.Pro77Pro |
S202 |
| 17474 | BAA01g13160 | A01 | 6243926 | G | A | upstream_gene_variant | MODIFIER | c.-716C>T| |
S239 |
| 17475 | BAA01g13160 | A01 | 6245195 | C | T | upstream_gene_variant | MODIFIER | c.-1985G>A| |
S130 |