Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g20190 | A05 | 12322198 | G | A | upstream_gene_variant | MODIFIER | c.-4927G>A| |
S129 |
2 | BAA05g20190 | A05 | 12322371 | C | T | upstream_gene_variant | MODIFIER | c.-4754C>T| |
S193 |
3 | BAA05g20190 | A05 | 12323059 | C | T | upstream_gene_variant | MODIFIER | c.-4066C>T| |
S106 |
4 | BAA05g20190 | A05 | 12323667 | C | T | upstream_gene_variant | MODIFIER | c.-3458C>T| |
S281 |
5 | BAA05g20190 | A05 | 12324223 | G | A | upstream_gene_variant | MODIFIER | c.-2902G>A| |
S123 |
6 | BAA05g20190 | A05 | 12324489 | G | A | upstream_gene_variant | MODIFIER | c.-2636G>A| |
S282 |
7 | BAA05g20190 | A05 | 12325923 | C | T | upstream_gene_variant | MODIFIER | c.-1202C>T| |
S229 |
8 | BAA05g20190 | A05 | 12327446 | G | A | missense_variant | MODERATE | c.322G>A|p.Ala108Thr |
S158 |
9 | BAA05g20190 | A05 | 12327457 | C | T | synonymous_variant | LOW | c.333C>T|p.Ile111Ile |
S108 |
10 | BAA05g20190 | A05 | 12327806 | G | A | missense_variant | MODERATE | c.682G>A|p.Val228Ile |
S161 |
11 | BAA05g20190 | A05 | 12327976 | G | A | synonymous_variant | LOW | c.852G>A|p.Glu284Glu |
S288 |