| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 157451 | BAA02g05140 | A02 | 2263842 | C | T | intron_variant | MODIFIER | c.291-226C>T| |
S38 |
| 157452 | BAA02g05140 | A02 | 2264031 | G | A | intron_variant | MODIFIER | c.291-37G>A| |
S146 |
| 157453 | BAA02g05140 | A02 | 2264234 | C | T | intron_variant | MODIFIER | c.393-21C>T| |
S42 |
| 157454 | BAA02g05140 | A02 | 2266016 | C | T | missense_variant | MODERATE | c.1595C>T|p.Ser532Phe |
S200 |
| 157455 | BAA02g05150 | A02 | 2267493 | A | T | upstream_gene_variant | MODIFIER | c.-2355A>T| |
S9 |
| 157456 | BAA02g05150 | A02 | 2267495 | G | A | upstream_gene_variant | MODIFIER | c.-2353G>A| |
S107 |
| 157457 | BAA02g05150 | A02 | 2268581 | G | A | upstream_gene_variant | MODIFIER | c.-1267G>A| |
S176 |
| 157458 | BAA02g05150 | A02 | 2268604 | A | T | upstream_gene_variant | MODIFIER | c.-1244A>T| |
S221 |
| 157459 | BAA02g05150 | A02 | 2268700 | G | A | upstream_gene_variant | MODIFIER | c.-1148G>A| |
S228 |
| 157460 | BAA02g05160 | A02 | 2270744 | C | T | upstream_gene_variant | MODIFIER | c.-372C>T| |
S233 |
| 157461 | BAA02g05160 | A02 | 2272315 | G | A | missense_variant | MODERATE | c.1006G>A|p.Ala336Thr |
S133 |
| 157462 | BAA02g05170 | A02 | 2272479 | C | T | upstream_gene_variant | MODIFIER | c.-805C>T| |
S108 |
| 157463 | BAA02g05170 | A02 | 2273432 | C | T | missense_variant | MODERATE | c.149C>T|p.Ser50Phe |
S298 |
| 157464 | BAA02g05170 | A02 | 2273538 | C | T | synonymous_variant | LOW | c.255C>T|p.Leu85Leu |
S240 |
| 157465 | BAA02g05170 | A02 | 2273607 | C | T | synonymous_variant | LOW | c.324C>T|p.Leu108Leu |
S230 |
| 157466 | BAA02g05170 | A02 | 2273730 | G | A | stop_gained | HIGH | c.447G>A|p.Trp149* |
S293 |
| 157467 | BAA02g05170 | A02 | 2273737 | C | T | missense_variant | MODERATE | c.454C>T|p.Leu152Phe |
S178 |
| 157468 | BAA02g05170 | A02 | 2274307 | G | A | missense_variant | MODERATE | c.1024G>A|p.Val342Met |
S202 |
| 157469 | BAA02g05170 | A02 | 2274398 | G | A | missense_variant | MODERATE | c.1115G>A|p.Gly372Asp |
S228 |
| 157470 | BAA02g05170 | A02 | 2275545 | C | T | missense_variant | MODERATE | c.1817C>T|p.Ser606Phe |
S85 |
| 157471 | BAA02g05170 | A02 | 2276069 | G | A | missense_variant | MODERATE | c.2233G>A|p.Val745Ile |
S275 |
| 157472 | BAA02g05170 | A02 | 2276387 | G | A | missense_variant | MODERATE | c.2551G>A|p.Ala851Thr |
S107 |
| 157473 | BAA02g05170 | A02 | 2276758 | G | A | synonymous_variant | LOW | c.2922G>A|p.Leu974Leu |
S271 |
| 157474 | BAA02g05180 | A02 | 2277686 | C | T | missense_variant | MODERATE | c.1543G>A|p.Val515Ile |
S9 |
| 157475 | BAA02g05180 | A02 | 2278049 | G | A | missense_variant | MODERATE | c.1247C>T|p.Thr416Ile |
S184 |