| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 191051 | BAA02g26260 | A02 | 14572057 | C | T | downstream_gene_variant | MODIFIER | c.*2904C>T| |
S241 |
| 191052 | BAA02g26260 | A02 | 14572206 | C | T | downstream_gene_variant | MODIFIER | c.*3053C>T| |
S142 |
| 191053 | BAA02g26270 | A02 | 14575469 | C | T | upstream_gene_variant | MODIFIER | c.-2513C>T| |
S238 |
| 191054 | BAA02g26270 | A02 | 14575799 | A | C | upstream_gene_variant | MODIFIER | c.-2183A>C| |
S96 |
| 191055 | BAA02g26270 | A02 | 14575993 | G | A | upstream_gene_variant | MODIFIER | c.-1989G>A| |
S38 |
| 191056 | BAA02g26270 | A02 | 14576226 | G | A | upstream_gene_variant | MODIFIER | c.-1756G>A| |
S278 |
| 191057 | BAA02g26270 | A02 | 14576233 | G | A | upstream_gene_variant | MODIFIER | c.-1749G>A| |
S126 |
| 191058 | BAA02g26270 | A02 | 14576764 | G | A | upstream_gene_variant | MODIFIER | c.-1218G>A| |
S251 |
| 191059 | BAA02g26270 | A02 | 14578000 | C | T | missense_variant | MODERATE | c.19C>T|p.Leu7Phe |
S287 |
| 191060 | BAA02g26270 | A02 | 14578007 | C | T | missense_variant | MODERATE | c.26C>T|p.Ser9Phe |
S180 |
| 191061 | BAA02g26270 | A02 | 14578163 | G | A | missense_variant | MODERATE | c.182G>A|p.Arg61His |
S161 |
| 191062 | BAA02g26270 | A02 | 14578202 | C | T | missense_variant | MODERATE | c.221C>T|p.Ser74Phe |
S224 |
| 191063 | BAA02g26270 | A02 | 14578264 | G | A | missense_variant | MODERATE | c.283G>A|p.Gly95Ser |
S56 |
| 191064 | BAA02g26270 | A02 | 14578405 | G | A | downstream_gene_variant | MODIFIER | c.*55G>A| |
S143 |
| 191065 | BAA02g26270 | A02 | 14578904 | G | A | downstream_gene_variant | MODIFIER | c.*554G>A| |
S279 |
| 191066 | BAA02g26270 | A02 | 14579666 | G | A | downstream_gene_variant | MODIFIER | c.*1316G>A| |
S60 |
| 191067 | BAA02g26270 | A02 | 14579919 | G | A | downstream_gene_variant | MODIFIER | c.*1569G>A| |
S125 |
| 191068 | BAA02g26280 | A02 | 14581785 | G | A | missense_variant | MODERATE | c.431C>T|p.Ala144Val |
S184 |
| 191069 | BAA02g26280 | A02 | 14582190 | C | T | missense_variant | MODERATE | c.109G>A|p.Ala37Thr |
S54 |
| 191070 | BAA02g26280 | A02 | 14584084 | G | A | upstream_gene_variant | MODIFIER | c.-1214C>T| |
S251 |
| 191071 | BAA02g26280 | A02 | 14584175 | C | T | upstream_gene_variant | MODIFIER | c.-1305G>A| |
S181 |
| 191072 | BAA02g26280 | A02 | 14584272 | C | T | upstream_gene_variant | MODIFIER | c.-1402G>A| |
S262 |
| 191073 | BAA02g26280 | A02 | 14584853 | C | T | upstream_gene_variant | MODIFIER | c.-1983G>A| |
S203 |
| 191074 | BAA02g26280 | A02 | 14586817 | G | A | upstream_gene_variant | MODIFIER | c.-3947C>T| |
S158 |
| 191075 | BAA02g26290 | A02 | 14588136 | G | A | downstream_gene_variant | MODIFIER | c.*3384C>T| |
S256 |