Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g00170 | A07 | 72215 | C | T | synonymous_variant | LOW | c.438G>A|p.Val146Val |
S38 |
2 | BAA07g00170 | A07 | 72487 | C | T | missense_variant | MODERATE | c.166G>A|p.Gly56Ser |
S233 |
3 | BAA07g00170 | A07 | 72976 | C | T | upstream_gene_variant | MODIFIER | c.-324G>A| |
S183 S198 |
4 | BAA07g00170 | A07 | 74267 | G | A | upstream_gene_variant | MODIFIER | c.-1615C>T| |
S229 |
5 | BAA07g00170 | A07 | 74593 | G | A | upstream_gene_variant | MODIFIER | c.-1941C>T| |
S244 |
6 | BAA07g00170 | A07 | 76237 | G | A | upstream_gene_variant | MODIFIER | c.-3585C>T| |
S251 |
7 | BAA07g00170 | A07 | 76239 | G | A | upstream_gene_variant | MODIFIER | c.-3587C>T| |
S105 S106 |
8 | BAA07g00170 | A07 | 76904 | T | C | upstream_gene_variant | MODIFIER | c.-4252A>G| |
S61 |
9 | BAA07g00170 | A07 | 77544 | G | A | upstream_gene_variant | MODIFIER | c.-4892C>T| |
S40 S49 |