Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g41900 | A05 | 39843634 | C | T | missense_variant | MODERATE | c.52G>A|p.Ala18Thr |
S192 |
2 | BAA05g41900 | A05 | 39845843 | G | A | upstream_gene_variant | MODIFIER | c.-2158C>T| |
S211 |
3 | BAA05g41900 | A05 | 39846109 | G | A | upstream_gene_variant | MODIFIER | c.-2424C>T| |
S229 |
4 | BAA05g41900 | A05 | 39846510 | C | T | upstream_gene_variant | MODIFIER | c.-2825G>A| |
S172 S217 |
5 | BAA05g41900 | A05 | 39846930 | G | A | upstream_gene_variant | MODIFIER | c.-3245C>T| |
S59 |
6 | BAA05g41900 | A05 | 39847989 | C | T | upstream_gene_variant | MODIFIER | c.-4304G>A| |
S245 |