Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g41740 | A02 | 34929456 | G | A | missense_variant | MODERATE | c.1114C>T|p.Pro372Ser |
S36 |
2 | BAA02g41740 | A02 | 34931525 | C | T | missense_variant | MODERATE | c.409G>A|p.Glu137Lys |
S269 |
3 | BAA02g41740 | A02 | 34931533 | C | T | missense_variant | MODERATE | c.401G>A|p.Cys134Tyr |
S107 |
4 | BAA02g41740 | A02 | 34931544 | C | T | synonymous_variant | LOW | c.390G>A|p.Thr130Thr |
S296 |
5 | BAA02g41740 | A02 | 34934179 | C | T | upstream_gene_variant | MODIFIER | c.-2246G>A| |
S13 S162 |
6 | BAA02g41740 | A02 | 34934260 | C | A | upstream_gene_variant | MODIFIER | c.-2327G>T| |
S223 |
7 | BAA02g41740 | A02 | 34934851 | G | A | upstream_gene_variant | MODIFIER | c.-2918C>T| |
S177 |
8 | BAA02g41740 | A02 | 34934941 | G | A | upstream_gene_variant | MODIFIER | c.-3008C>T| |
S50 |
9 | BAA02g41740 | A02 | 34936743 | G | A | upstream_gene_variant | MODIFIER | c.-4810C>T| |
S294 |