Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g38750 | A01 | 25841784 | G | A | missense_variant | MODERATE | c.503C>T|p.Thr168Ile |
S13 |
2 | BAA01g38750 | A01 | 25844703 | C | T | upstream_gene_variant | MODIFIER | c.-1149G>A| |
S284 |
3 | BAA01g38750 | A01 | 25845260 | C | T | upstream_gene_variant | MODIFIER | c.-1706G>A| |
S233 |
4 | BAA01g38750 | A01 | 25848068 | C | T | upstream_gene_variant | MODIFIER | c.-4514G>A| |
S156 |
5 | BAA01g38750 | A01 | 25848173 | C | T | upstream_gene_variant | MODIFIER | c.-4619G>A| |
S115 |
6 | BAA01g38750 | A01 | 25848498 | G | A | upstream_gene_variant | MODIFIER | c.-4944C>T| |
S189 |