Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g43660 | A02 | 36130993 | G | A | missense_variant | MODERATE | c.595C>T|p.Pro199Ser |
S113 |
2 | BAA02g43660 | A02 | 36132347 | C | T | upstream_gene_variant | MODIFIER | c.-760G>A| |
S17 |
3 | BAA02g43660 | A02 | 36132497 | C | T | upstream_gene_variant | MODIFIER | c.-910G>A| |
S16 |
4 | BAA02g43660 | A02 | 36134367 | C | T | upstream_gene_variant | MODIFIER | c.-2780G>A| |
S171 |
5 | BAA02g43660 | A02 | 36134597 | G | A | upstream_gene_variant | MODIFIER | c.-3010C>T| |
S223 |
6 | BAA02g43660 | A02 | 36136460 | G | A | upstream_gene_variant | MODIFIER | c.-4873C>T| |
S36 |