Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00920 | A02 | 426223 | C | T | synonymous_variant | LOW | c.69C>T|p.Pro23Pro |
S200 |
2 | BAA02g00920 | A02 | 426545 | C | T | missense_variant | MODERATE | c.391C>T|p.His131Tyr |
S174 |
3 | BAA02g00920 | A02 | 427901 | G | A | downstream_gene_variant | MODIFIER | c.*85G>A| |
S12 |
4 | BAA02g00920 | A02 | 429292 | G | A | downstream_gene_variant | MODIFIER | c.*1476G>A| |
S266 |
5 | BAA02g00920 | A02 | 429480 | C | T | downstream_gene_variant | MODIFIER | c.*1664C>T| |
S181 |
6 | BAA02g00920 | A02 | 429775 | G | A | downstream_gene_variant | MODIFIER | c.*1959G>A| |
S202 |
7 | BAA02g00920 | A02 | 430189 | G | A | downstream_gene_variant | MODIFIER | c.*2373G>A| |
S36 |
8 | BAA02g00920 | A02 | 430873 | C | T | downstream_gene_variant | MODIFIER | c.*3057C>T| |
S202 |
9 | BAA02g00920 | A02 | 431138 | C | T | downstream_gene_variant | MODIFIER | c.*3322C>T| |
S116 |
10 | BAA02g00920 | A02 | 431487 | C | T | downstream_gene_variant | MODIFIER | c.*3671C>T| |
S71 |
11 | BAA02g00920 | A02 | 431592 | G | A | downstream_gene_variant | MODIFIER | c.*3776G>A| |
S70 |