Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g66920 | A03 | 41443033 | G | A | downstream_gene_variant | MODIFIER | c.*4790C>T| |
S64 |
2 | BAA03g66920 | A03 | 41443160 | C | T | downstream_gene_variant | MODIFIER | c.*4663G>A| |
S188 |
3 | BAA03g66920 | A03 | 41443475 | G | A | downstream_gene_variant | MODIFIER | c.*4348C>T| |
S210 |
4 | BAA03g66920 | A03 | 41448299 | C | T | missense_variant | MODERATE | c.712G>A|p.Ala238Thr |
S32 |
5 | BAA03g66920 | A03 | 41448679 | G | A | missense_variant | MODERATE | c.332C>T|p.Ser111Phe |
S191 |
6 | BAA03g66920 | A03 | 41449403 | C | T | upstream_gene_variant | MODIFIER | c.-393G>A| |
S256 |
7 | BAA03g66920 | A03 | 41449427 | G | A | upstream_gene_variant | MODIFIER | c.-417C>T| |
S80 |
8 | BAA03g66920 | A03 | 41449591 | T | A | upstream_gene_variant | MODIFIER | c.-581A>T| |
S205 S222 S227 S240 S247 S258 S281 S282 |
9 | BAA03g66920 | A03 | 41450216 | C | T | upstream_gene_variant | MODIFIER | c.-1206G>A| |
S187 |
10 | BAA03g66920 | A03 | 41450472 | G | A | upstream_gene_variant | MODIFIER | c.-1462C>T| |
S146 |
11 | BAA03g66920 | A03 | 41450815 | G | A | upstream_gene_variant | MODIFIER | c.-1805C>T| |
S155 |
12 | BAA03g66920 | A03 | 41450905 | C | T | upstream_gene_variant | MODIFIER | c.-1895G>A| |
S203 |
13 | BAA03g66920 | A03 | 41450983 | G | A | upstream_gene_variant | MODIFIER | c.-1973C>T| |
S174 |
14 | BAA03g66920 | A03 | 41451366 | G | A | upstream_gene_variant | MODIFIER | c.-2356C>T| |
S73 S91 |
15 | BAA03g66920 | A03 | 41451990 | G | A | upstream_gene_variant | MODIFIER | c.-2980C>T| |
S160 |
16 | BAA03g66920 | A03 | 41453754 | G | A | upstream_gene_variant | MODIFIER | c.-4744C>T| |
S132 S137 S215 S89 |