Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g20280 | A04 | 23448155 | C | T | missense_variant | MODERATE | c.266C>T|p.Thr89Ile |
S168 |
2 | BAA04g20280 | A04 | 23448955 | C | T | synonymous_variant | LOW | c.651C>T|p.Ser217Ser |
S32 |
3 | BAA04g20280 | A04 | 23451009 | G | A | synonymous_variant | LOW | c.1227G>A|p.Leu409Leu |
S288 |
4 | BAA04g20280 | A04 | 23452168 | C | T | downstream_gene_variant | MODIFIER | c.*862C>T| |
S308 |
5 | BAA04g20280 | A04 | 23452353 | C | T | downstream_gene_variant | MODIFIER | c.*1047C>T| |
S47 |
6 | BAA04g20280 | A04 | 23454544 | G | A | downstream_gene_variant | MODIFIER | c.*3238G>A| |
S179 |
7 | BAA04g20280 | A04 | 23455138 | C | T | downstream_gene_variant | MODIFIER | c.*3832C>T| |
S247 |