| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 154551 | BAA02g02800 | A02 | 1268807 | G | A | upstream_gene_variant | MODIFIER | c.-754G>A| |
S259 |
| 154552 | BAA02g02800 | A02 | 1269185 | G | A | upstream_gene_variant | MODIFIER | c.-376G>A| |
S208 S93 |
| 154553 | BAA02g02800 | A02 | 1269478 | C | T | upstream_gene_variant | MODIFIER | c.-83C>T| |
S115 |
| 154554 | BAA02g02800 | A02 | 1270155 | G | A | synonymous_variant | LOW | c.288G>A|p.Lys96Lys |
S190 |
| 154555 | BAA02g02810 | A02 | 1271195 | G | A | upstream_gene_variant | MODIFIER | c.-139G>A| |
S208 S57 S93 |
| 154556 | BAA02g02800 | A02 | 1271713 | G | A | downstream_gene_variant | MODIFIER | c.*1537G>A| |
S260 |
| 154557 | BAA02g02810 | A02 | 1272475 | G | C | missense_variant | MODERATE | c.445G>C|p.Asp149His |
S170 |
| 154558 | BAA02g02810 | A02 | 1272705 | G | A | synonymous_variant | LOW | c.675G>A|p.Glu225Glu |
S241 |
| 154559 | BAA02g02800 | A02 | 1273447 | C | A | downstream_gene_variant | MODIFIER | c.*3271C>A| |
S74 |
| 154560 | BAA02g02820 | A02 | 1274303 | C | T | missense_variant | MODERATE | c.578G>A|p.Gly193Asp |
S281 |
| 154561 | BAA02g02820 | A02 | 1274330 | G | A | missense_variant | MODERATE | c.551C>T|p.Ala184Val |
S149 S93 |
| 154562 | BAA02g02820 | A02 | 1275746 | G | A | missense_variant | MODERATE | c.88C>T|p.Leu30Phe |
S209 |
| 154563 | BAA02g02820 | A02 | 1277843 | C | T | upstream_gene_variant | MODIFIER | c.-2010G>A| |
S82 S92 |
| 154564 | BAA02g02820 | A02 | 1278227 | G | A | upstream_gene_variant | MODIFIER | c.-2394C>T| |
S282 |
| 154565 | BAA02g02820 | A02 | 1278267 | C | T | upstream_gene_variant | MODIFIER | c.-2434G>A| |
S211 S227 |
| 154566 | BAA02g02820 | A02 | 1278451 | C | T | upstream_gene_variant | MODIFIER | c.-2618G>A| |
S207 |
| 154567 | BAA02g02820 | A02 | 1278751 | C | T | upstream_gene_variant | MODIFIER | c.-2918G>A| |
S229 |
| 154568 | BAA02g02820 | A02 | 1278886 | C | T | upstream_gene_variant | MODIFIER | c.-3053G>A| |
S116 |
| 154569 | BAA02g02830 | A02 | 1279915 | C | T | missense_variant | MODERATE | c.121C>T|p.Pro41Ser |
S130 |
| 154570 | BAA02g02830 | A02 | 1279976 | C | T | missense_variant | MODERATE | c.182C>T|p.Thr61Ile |
S216 |
| 154571 | BAA02g02830 | A02 | 1280623 | G | A | missense_variant | MODERATE | c.542G>A|p.Gly181Asp |
S43 |
| 154572 | BAA02g02830 | A02 | 1280705 | C | T | splice_region_variant&intron_variant | LOW | c.618+6C>T| |
S249 |
| 154573 | BAA02g02830 | A02 | 1281914 | G | A | downstream_gene_variant | MODIFIER | c.*249G>A| |
S68 |
| 154574 | BAA02g02840 | A02 | 1282366 | G | A | missense_variant | MODERATE | c.634C>T|p.Pro212Ser |
S132 S137 S215 S89 |
| 154575 | BAA02g02840 | A02 | 1283402 | G | A | upstream_gene_variant | MODIFIER | c.-293C>T| |
S107 |