Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g12990 | A05 | 6713688 | C | T | missense_variant | MODERATE | c.308G>A|p.Gly103Glu |
S189 |
2 | BAA05g12990 | A05 | 6714719 | G | A | upstream_gene_variant | MODIFIER | c.-28C>T| |
S258 |
3 | BAA05g12990 | A05 | 6714841 | C | T | upstream_gene_variant | MODIFIER | c.-150G>A| |
S229 |
4 | BAA05g12990 | A05 | 6715490 | G | A | upstream_gene_variant | MODIFIER | c.-799C>T| |
S11 |
5 | BAA05g12990 | A05 | 6715900 | C | T | upstream_gene_variant | MODIFIER | c.-1209G>A| |
S12 |
6 | BAA05g12990 | A05 | 6717338 | G | A | upstream_gene_variant | MODIFIER | c.-2647C>T| |
S262 |
7 | BAA05g12990 | A05 | 6717444 | C | T | upstream_gene_variant | MODIFIER | c.-2753G>A| |
S130 |
8 | BAA05g12990 | A05 | 6717534 | C | T | upstream_gene_variant | MODIFIER | c.-2843G>A| |
S33 |
9 | BAA05g12990 | A05 | 6719673 | C | T | upstream_gene_variant | MODIFIER | c.-4982G>A| |
S166 |