| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 74451 | BAA01g39140 | A01 | 26037712 | G | A | downstream_gene_variant | MODIFIER | c.*3479G>A| |
S153 S157 S236 S257 S262 S263 |
| 74452 | BAA01g39160 | A01 | 26038340 | G | A | missense_variant | MODERATE | c.1529C>T|p.Ser510Phe |
S152 |
| 74453 | BAA01g39160 | A01 | 26039258 | C | T | missense_variant | MODERATE | c.853G>A|p.Ala285Thr |
S288 |
| 74454 | BAA01g39160 | A01 | 26039843 | G | A | missense_variant | MODERATE | c.541C>T|p.Pro181Ser |
S173 |
| 74455 | BAA01g39160 | A01 | 26039975 | G | A | missense_variant | MODERATE | c.409C>T|p.Arg137Cys |
S262 |
| 74456 | BAA01g39160 | A01 | 26040193 | G | A | missense_variant | MODERATE | c.191C>T|p.Ser64Phe |
S160 |
| 74457 | BAA01g39160 | A01 | 26040263 | C | T | missense_variant | MODERATE | c.121G>A|p.Ala41Thr |
S100 |
| 74458 | BAA01g39160 | A01 | 26040326 | C | T | missense_variant | MODERATE | c.58G>A|p.Gly20Ser |
S203 |
| 74459 | BAA01g39160 | A01 | 26040518 | C | T | upstream_gene_variant | MODIFIER | c.-48G>A| |
S302 |
| 74460 | BAA01g39160 | A01 | 26041543 | G | A | upstream_gene_variant | MODIFIER | c.-1073C>T| |
S199 |
| 74461 | BAA01g39160 | A01 | 26041628 | G | A | upstream_gene_variant | MODIFIER | c.-1158C>T| |
S260 |
| 74462 | BAA01g39170 | A01 | 26044484 | C | T | missense_variant | MODERATE | c.911G>A|p.Gly304Glu |
S139 |
| 74463 | BAA01g39170 | A01 | 26044512 | G | A | missense_variant | MODERATE | c.883C>T|p.Leu295Phe |
S79 S91 |
| 74464 | BAA01g39160 | A01 | 26045345 | G | A | upstream_gene_variant | MODIFIER | c.-4875C>T| |
S35 |
| 74465 | BAA01g39180 | A01 | 26048071 | G | A | missense_variant | MODERATE | c.280G>A|p.Asp94Asn |
S122 |
| 74466 | BAA01g39180 | A01 | 26048210 | C | T | missense_variant | MODERATE | c.322C>T|p.Pro108Ser |
S251 |
| 74467 | BAA01g39170 | A01 | 26048461 | C | T | upstream_gene_variant | MODIFIER | c.-2422G>A| |
S200 |
| 74468 | BAA01g39170 | A01 | 26049571 | G | A | upstream_gene_variant | MODIFIER | c.-3532C>T| |
S6 |
| 74469 | BAA01g39170 | A01 | 26049635 | C | T | upstream_gene_variant | MODIFIER | c.-3596G>A| |
S74 |
| 74470 | BAA01g39170 | A01 | 26049637 | C | T | upstream_gene_variant | MODIFIER | c.-3598G>A| |
S127 |
| 74471 | BAA01g39190 | A01 | 26052297 | C | T | missense_variant | MODERATE | c.569G>A|p.Gly190Glu |
S233 |
| 74472 | BAA01g39190 | A01 | 26053507 | G | A | upstream_gene_variant | MODIFIER | c.-456C>T| |
S13 S189 |
| 74473 | BAA01g39220 | A01 | 26057692 | C | T | missense_variant | MODERATE | c.1474G>A|p.Val492Ile |
S32 |
| 74474 | BAA01g39220 | A01 | 26058729 | G | A | missense_variant | MODERATE | c.587C>T|p.Pro196Leu |
S286 |
| 74475 | BAA01g39200 | A01 | 26058864 | C | T | upstream_gene_variant | MODIFIER | c.-4675G>A| |
S293 |