Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g36180 | A02 | 31052447 | G | A | missense_variant | MODERATE | c.3157C>T|p.Pro1053Ser |
S110 |
2 | BAA02g36180 | A02 | 31052575 | C | T | missense_variant | MODERATE | c.3029G>A|p.Gly1010Glu |
S242 |
3 | BAA02g36180 | A02 | 31052588 | G | A | missense_variant | MODERATE | c.3016C>T|p.His1006Tyr |
S45 |
4 | BAA02g36180 | A02 | 31054911 | G | A | synonymous_variant | LOW | c.693C>T|p.Ser231Ser |
S26 |
5 | BAA02g36180 | A02 | 31057078 | G | A | upstream_gene_variant | MODIFIER | c.-1475C>T| |
S306 S308 |
6 | BAA02g36180 | A02 | 31059487 | G | A | upstream_gene_variant | MODIFIER | c.-3884C>T| |
S45 |
7 | BAA02g36180 | A02 | 31059519 | C | T | upstream_gene_variant | MODIFIER | c.-3916G>A| |
S276 |
8 | BAA02g36180 | A02 | 31060528 | G | A | upstream_gene_variant | MODIFIER | c.-4925C>T| |
S90 |