Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g18930 | A02 | 9783818 | C | T | missense_variant | MODERATE | c.1129G>A|p.Asp377Asn |
S289 S290 |
2 | BAA02g18930 | A02 | 9784372 | C | T | synonymous_variant | LOW | c.687G>A|p.Val229Val |
S123 |
3 | BAA02g18930 | A02 | 9784738 | C | T | missense_variant | MODERATE | c.391G>A|p.Asp131Asn |
S179 |
4 | BAA02g18930 | A02 | 9784980 | G | A | missense_variant | MODERATE | c.149C>T|p.Ser50Phe |
S110 |
5 | BAA02g18930 | A02 | 9785070 | G | A | missense_variant | MODERATE | c.59C>T|p.Ser20Phe |
S69 |
6 | BAA02g18930 | A02 | 9788524 | C | T | upstream_gene_variant | MODIFIER | c.-3396G>A| |
S118 |
7 | BAA02g18930 | A02 | 9789037 | G | A | upstream_gene_variant | MODIFIER | c.-3909C>T| |
S13 S140 S168 S279 S64 |
8 | BAA02g18930 | A02 | 9789199 | C | T | upstream_gene_variant | MODIFIER | c.-4071G>A| |
S161 |
9 | BAA02g18930 | A02 | 9789522 | G | A | upstream_gene_variant | MODIFIER | c.-4394C>T| |
S116 |
10 | BAA02g18930 | A02 | 9789705 | C | T | upstream_gene_variant | MODIFIER | c.-4577G>A| |
S242 |