Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g13770 | A02 | 6419214 | G | A | missense_variant | MODERATE | c.572C>T|p.Ala191Val |
S36 |
2 | BAA02g13770 | A02 | 6419333 | G | A | intron_variant | MODIFIER | c.525+12C>T| |
S203 |
3 | BAA02g13770 | A02 | 6419612 | G | A | intron_variant | MODIFIER | c.268-10C>T| |
S144 |
4 | BAA02g13770 | A02 | 6420276 | C | T | upstream_gene_variant | MODIFIER | c.-194G>A| |
S182 |
5 | BAA02g13770 | A02 | 6422579 | G | A | upstream_gene_variant | MODIFIER | c.-2497C>T| |
S302 |
6 | BAA02g13770 | A02 | 6422615 | G | A | upstream_gene_variant | MODIFIER | c.-2533C>T| |
S203 |
7 | BAA02g13770 | A02 | 6423495 | C | T | upstream_gene_variant | MODIFIER | c.-3413G>A| |
S120 |
8 | BAA02g13770 | A02 | 6423567 | G | A | upstream_gene_variant | MODIFIER | c.-3485C>T| |
S256 |
9 | BAA02g13770 | A02 | 6424639 | C | T | upstream_gene_variant | MODIFIER | c.-4557G>A| |
S13 |