Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g55060 | A09 | 55379505 | C | T | missense_variant | MODERATE | c.2030G>A|p.Gly677Asp |
S8 |
2 | BAA09g55060 | A09 | 55379627 | G | A | synonymous_variant | LOW | c.1908C>T|p.Asp636Asp |
S210 |
3 | BAA09g55060 | A09 | 55380146 | G | A | splice_region_variant&intron_variant | LOW | c.1684-5C>T| |
S255 |
4 | BAA09g55060 | A09 | 55380256 | C | T | missense_variant | MODERATE | c.1670G>A|p.Gly557Glu |
S17 |
5 | BAA09g55060 | A09 | 55380683 | C | T | missense_variant | MODERATE | c.1324G>A|p.Gly442Arg |
S109 |
6 | BAA09g55060 | A09 | 55381812 | C | T | synonymous_variant | LOW | c.627G>A|p.Thr209Thr |
S306 S308 |
7 | BAA09g55060 | A09 | 55381882 | C | T | missense_variant | MODERATE | c.557G>A|p.Arg186Gln |
S205 |
8 | BAA09g55060 | A09 | 55382828 | C | T | upstream_gene_variant | MODIFIER | c.-76G>A| |
S56 |
9 | BAA09g55060 | A09 | 55383357 | C | T | upstream_gene_variant | MODIFIER | c.-605G>A| |
S192 |
10 | BAA09g55060 | A09 | 55384223 | G | A | upstream_gene_variant | MODIFIER | c.-1471C>T| |
S135 |
11 | BAA09g55060 | A09 | 55386366 | C | T | upstream_gene_variant | MODIFIER | c.-3614G>A| |
S107 |
12 | BAA09g55060 | A09 | 55386654 | G | A | upstream_gene_variant | MODIFIER | c.-3902C>T| |
S87 |