Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g12000 | A05 | 6070866 | C | T | missense_variant | MODERATE | c.712G>A|p.Gly238Ser |
S132 S137 S215 |
2 | BAA05g12000 | A05 | 6071171 | C | T | missense_variant | MODERATE | c.407G>A|p.Ser136Asn |
S176 |
3 | BAA05g12000 | A05 | 6071593 | C | T | upstream_gene_variant | MODIFIER | c.-16G>A| |
S140 |
4 | BAA05g12000 | A05 | 6072229 | G | A | upstream_gene_variant | MODIFIER | c.-652C>T| |
S104 |
5 | BAA05g12000 | A05 | 6072651 | G | A | upstream_gene_variant | MODIFIER | c.-1074C>T| |
S138 |
6 | BAA05g12000 | A05 | 6074406 | C | T | upstream_gene_variant | MODIFIER | c.-2829G>A| |
S130 |
7 | BAA05g12000 | A05 | 6074627 | G | A | upstream_gene_variant | MODIFIER | c.-3050C>T| |
S208 |
8 | BAA05g12000 | A05 | 6075216 | C | T | upstream_gene_variant | MODIFIER | c.-3639G>A| |
S10 |
9 | BAA05g12000 | A05 | 6075599 | C | T | upstream_gene_variant | MODIFIER | c.-4022G>A| |
S148 S30 S31 |
10 | BAA05g12000 | A05 | 6076256 | G | A | upstream_gene_variant | MODIFIER | c.-4679C>T| |
S247 |