Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g16530 | A02 | 8084675 | G | A | missense_variant | MODERATE | c.1667C>T|p.Pro556Leu |
S80 |
2 | BAA02g16530 | A02 | 8085187 | C | T | synonymous_variant | LOW | c.1155G>A|p.Glu385Glu |
S54 |
3 | BAA02g16530 | A02 | 8085196 | G | C | synonymous_variant | LOW | c.1146C>G|p.Thr382Thr |
S54 |
4 | BAA02g16530 | A02 | 8085210 | C | T | missense_variant | MODERATE | c.1132G>A|p.Val378Ile |
S219 S72 |
5 | BAA02g16530 | A02 | 8086553 | G | A | missense_variant | MODERATE | c.47C>T|p.Pro16Leu |
S52 |
6 | BAA02g16530 | A02 | 8088740 | C | T | upstream_gene_variant | MODIFIER | c.-2141G>A| |
S117 |
7 | BAA02g16530 | A02 | 8091307 | C | T | upstream_gene_variant | MODIFIER | c.-4708G>A| |
S77 S82 |