Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g15400 | A01 | 7418179 | C | T | upstream_gene_variant | MODIFIER | c.-4317C>T| |
S128 |
2 | BAA01g15400 | A01 | 7419420 | C | T | upstream_gene_variant | MODIFIER | c.-3076C>T| |
S138 |
3 | BAA01g15400 | A01 | 7419663 | C | T | upstream_gene_variant | MODIFIER | c.-2833C>T| |
S179 |
4 | BAA01g15400 | A01 | 7421065 | C | T | upstream_gene_variant | MODIFIER | c.-1431C>T| |
S118 |
5 | BAA01g15400 | A01 | 7422319 | C | T | upstream_gene_variant | MODIFIER | c.-177C>T| |
S4 |
6 | BAA01g15400 | A01 | 7422338 | A | C | upstream_gene_variant | MODIFIER | c.-158A>C| |
S4 |
7 | BAA01g15400 | A01 | 7422727 | G | A | missense_variant | MODERATE | c.232G>A|p.Asp78Asn |
S187 |
8 | BAA01g15400 | A01 | 7423590 | G | A | missense_variant | MODERATE | c.658G>A|p.Val220Met |
S59 |
9 | BAA01g15400 | A01 | 7423696 | G | A | missense_variant | MODERATE | c.764G>A|p.Gly255Glu |
S116 |
10 | BAA01g15400 | A01 | 7424828 | C | T | downstream_gene_variant | MODIFIER | c.*1005C>T| |
S198 |
11 | BAA01g15400 | A01 | 7425631 | G | A | downstream_gene_variant | MODIFIER | c.*1808G>A| |
S183 |
12 | BAA01g15400 | A01 | 7427361 | C | T | downstream_gene_variant | MODIFIER | c.*3538C>T| |
S184 |
13 | BAA01g15400 | A01 | 7427415 | C | T | downstream_gene_variant | MODIFIER | c.*3592C>T| |
S295 |