Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g01950 | A05 | 1058444 | C | T | missense_variant | MODERATE | c.413G>A|p.Gly138Glu |
S229 |
2 | BAA05g01950 | A05 | 1058922 | G | A | upstream_gene_variant | MODIFIER | c.-66C>T| |
S134 |
3 | BAA05g01950 | A05 | 1059064 | G | A | upstream_gene_variant | MODIFIER | c.-208C>T| |
S14 |
4 | BAA05g01950 | A05 | 1059702 | C | T | upstream_gene_variant | MODIFIER | c.-846G>A| |
S163 |
5 | BAA05g01950 | A05 | 1059799 | C | T | upstream_gene_variant | MODIFIER | c.-943G>A| |
S189 |
6 | BAA05g01950 | A05 | 1060935 | C | T | upstream_gene_variant | MODIFIER | c.-2079G>A| |
S94 |
7 | BAA05g01950 | A05 | 1061003 | G | A | upstream_gene_variant | MODIFIER | c.-2147C>T| |
S148 S210 |
8 | BAA05g01950 | A05 | 1061747 | G | A | upstream_gene_variant | MODIFIER | c.-2891C>T| |
S122 |
9 | BAA05g01950 | A05 | 1062101 | C | T | upstream_gene_variant | MODIFIER | c.-3245G>A| |
S287 |
10 | BAA05g01950 | A05 | 1062847 | C | T | upstream_gene_variant | MODIFIER | c.-3991G>A| |
S36 |