| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 192451 | BAA02g26960 | A02 | 15105542 | G | A | synonymous_variant | LOW | c.3909C>T|p.Phe1303Phe |
S161 |
| 192452 | BAA02g26950 | A02 | 15105941 | C | T | upstream_gene_variant | MODIFIER | c.-3047G>A| |
S179 |
| 192453 | BAA02g26960 | A02 | 15106986 | C | T | missense_variant | MODERATE | c.2806G>A|p.Glu936Lys |
S131 |
| 192454 | BAA02g26950 | A02 | 15107137 | G | A | upstream_gene_variant | MODIFIER | c.-4243C>T| |
S306 S308 |
| 192455 | BAA02g26960 | A02 | 15107174 | G | A | synonymous_variant | LOW | c.2712C>T|p.Leu904Leu |
S169 |
| 192456 | BAA02g26960 | A02 | 15107448 | G | A | missense_variant | MODERATE | c.2438C>T|p.Ser813Phe |
S173 |
| 192457 | BAA02g26960 | A02 | 15107643 | G | A | missense_variant | MODERATE | c.2243C>T|p.Pro748Leu |
S80 |
| 192458 | BAA02g26960 | A02 | 15108595 | G | A | missense_variant | MODERATE | c.1291C>T|p.His431Tyr |
S59 |
| 192459 | BAA02g26960 | A02 | 15109298 | G | A | missense_variant | MODERATE | c.805C>T|p.Pro269Ser |
S228 |
| 192460 | BAA02g26960 | A02 | 15109348 | G | A | missense_variant | MODERATE | c.755C>T|p.Ser252Phe |
S235 |
| 192461 | BAA02g26960 | A02 | 15109398 | C | T | synonymous_variant | LOW | c.705G>A|p.Gln235Gln |
S144 |
| 192462 | BAA02g26960 | A02 | 15109737 | G | A | missense_variant | MODERATE | c.445C>T|p.Pro149Ser |
S303 |
| 192463 | BAA02g26960 | A02 | 15110708 | C | T | upstream_gene_variant | MODIFIER | c.-335G>A| |
S115 |
| 192464 | BAA02g26960 | A02 | 15111134 | C | T | upstream_gene_variant | MODIFIER | c.-761G>A| |
S280 |
| 192465 | BAA02g26960 | A02 | 15112980 | C | T | upstream_gene_variant | MODIFIER | c.-2607G>A| |
S301 S304 |
| 192466 | BAA02g26960 | A02 | 15114445 | C | T | upstream_gene_variant | MODIFIER | c.-4072G>A| |
S42 |
| 192467 | BAA02g26960 | A02 | 15114897 | G | A | upstream_gene_variant | MODIFIER | c.-4524C>T| |
S35 |
| 192468 | BAA02g26960 | A02 | 15115241 | G | A | upstream_gene_variant | MODIFIER | c.-4868C>T| |
S92 |
| 192469 | BAA02g26960 | A02 | 15115248 | C | T | upstream_gene_variant | MODIFIER | c.-4875G>A| |
S284 |
| 192470 | BAA02g26970 | A02 | 15115719 | G | A | missense_variant | MODERATE | c.220G>A|p.Asp74Asn |
S13 |
| 192471 | BAA02g26970 | A02 | 15117220 | G | A | missense_variant | MODERATE | c.411G>A|p.Met137Ile |
S256 |
| 192472 | BAA02g26980 | A02 | 15117396 | G | A | upstream_gene_variant | MODIFIER | c.-2885G>A| |
S208 |
| 192473 | BAA02g26980 | A02 | 15117596 | G | A | upstream_gene_variant | MODIFIER | c.-2685G>A| |
S13 |
| 192474 | BAA02g26980 | A02 | 15118155 | G | A | upstream_gene_variant | MODIFIER | c.-2126G>A| |
S247 |
| 192475 | BAA02g26990 | A02 | 15130125 | C | T | missense_variant | MODERATE | c.676G>A|p.Glu226Lys |
S274 |