Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g37890 | A02 | 32404429 | C | T | downstream_gene_variant | MODIFIER | c.*2164G>A| |
S139 |
2 | BAA02g37890 | A02 | 32404578 | C | T | downstream_gene_variant | MODIFIER | c.*2015G>A| |
S116 |
3 | BAA02g37890 | A02 | 32404769 | G | A | downstream_gene_variant | MODIFIER | c.*1824C>T| |
S237 |
4 | BAA02g37890 | A02 | 32405311 | G | A | downstream_gene_variant | MODIFIER | c.*1282C>T| |
S188 |
5 | BAA02g37890 | A02 | 32405541 | C | T | downstream_gene_variant | MODIFIER | c.*1052G>A| |
S180 |
6 | BAA02g37890 | A02 | 32406044 | G | A | downstream_gene_variant | MODIFIER | c.*549C>T| |
S95 |
7 | BAA02g37890 | A02 | 32406156 | G | A | downstream_gene_variant | MODIFIER | c.*437C>T| |
S235 |
8 | BAA02g37890 | A02 | 32406362 | C | T | downstream_gene_variant | MODIFIER | c.*231G>A| |
S87 |
9 | BAA02g37890 | A02 | 32406897 | G | A | intron_variant | MODIFIER | c.532-176C>T| |
S221 |
10 | BAA02g37890 | A02 | 32407415 | C | T | missense_variant | MODERATE | c.438G>A|p.Met146Ile |
S273 |
11 | BAA02g37890 | A02 | 32410032 | G | A | upstream_gene_variant | MODIFIER | c.-2079C>T| |
S281 S282 |
12 | BAA02g37890 | A02 | 32411043 | G | A | upstream_gene_variant | MODIFIER | c.-3090C>T| |
S86 |
13 | BAA02g37890 | A02 | 32412937 | G | A | upstream_gene_variant | MODIFIER | c.-4984C>T| |
S246 |