Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g17060 | A09 | 10133966 | C | T | missense_variant | MODERATE | c.1876G>A|p.Ala626Thr |
S287 |
2 | BAA09g17060 | A09 | 10133976 | C | T | stop_gained | HIGH | c.1866G>A|p.Trp622* |
S132 S137 S215 |
3 | BAA09g17060 | A09 | 10134025 | A | C | missense_variant | MODERATE | c.1817T>G|p.Leu606Arg |
S165 S211 S227 |
4 | BAA09g17060 | A09 | 10135116 | C | T | stop_gained | HIGH | c.810G>A|p.Trp270* |
S136 |
5 | BAA09g17060 | A09 | 10135124 | C | T | missense_variant | MODERATE | c.802G>A|p.Ala268Thr |
S296 |
6 | BAA09g17060 | A09 | 10137952 | G | A | upstream_gene_variant | MODIFIER | c.-1556C>T| |
S245 |
7 | BAA09g17060 | A09 | 10138090 | C | T | upstream_gene_variant | MODIFIER | c.-1694G>A| |
S177 |
8 | BAA09g17060 | A09 | 10138770 | G | A | upstream_gene_variant | MODIFIER | c.-2374C>T| |
S267 |
9 | BAA09g17060 | A09 | 10140512 | C | T | upstream_gene_variant | MODIFIER | c.-4116G>A| |
S239 |