Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g42470 | A05 | 40223134 | T | A | missense_variant | MODERATE | c.754A>T|p.Thr252Ser |
S11 |
2 | BAA05g42470 | A05 | 40223181 | G | A | missense_variant | MODERATE | c.707C>T|p.Ser236Phe |
S289 S290 |
3 | BAA05g42470 | A05 | 40223316 | G | A | missense_variant | MODERATE | c.572C>T|p.Ser191Leu |
S60 |
4 | BAA05g42470 | A05 | 40223345 | C | T | synonymous_variant | LOW | c.543G>A|p.Thr181Thr |
S212 |
5 | BAA05g42470 | A05 | 40223593 | G | A | missense_variant | MODERATE | c.295C>T|p.Leu99Phe |
S281 |
6 | BAA05g42470 | A05 | 40223606 | C | T | synonymous_variant | LOW | c.282G>A|p.Gly94Gly |
S66 |
7 | BAA05g42470 | A05 | 40223972 | C | T | upstream_gene_variant | MODIFIER | c.-85G>A| |
S236 |
8 | BAA05g42470 | A05 | 40224770 | C | T | upstream_gene_variant | MODIFIER | c.-883G>A| |
S194 |
9 | BAA05g42470 | A05 | 40226646 | G | A | upstream_gene_variant | MODIFIER | c.-2759C>T| |
S57 |
10 | BAA05g42470 | A05 | 40228256 | C | T | upstream_gene_variant | MODIFIER | c.-4369G>A| |
S45 |