Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g08990 | A02 | 3966533 | G | A | upstream_gene_variant | MODIFIER | c.-4232G>A| |
S92 |
2 | BAA02g08990 | A02 | 3968088 | A | C | upstream_gene_variant | MODIFIER | c.-2677A>C| |
S308 |
3 | BAA02g08990 | A02 | 3968707 | C | T | upstream_gene_variant | MODIFIER | c.-2058C>T| |
S278 |
4 | BAA02g08990 | A02 | 3969063 | G | A | upstream_gene_variant | MODIFIER | c.-1702G>A| |
S261 |
5 | BAA02g08990 | A02 | 3969378 | C | T | upstream_gene_variant | MODIFIER | c.-1387C>T| |
S77 S82 |
6 | BAA02g08990 | A02 | 3969402 | C | T | upstream_gene_variant | MODIFIER | c.-1363C>T| |
S62 |
7 | BAA02g08990 | A02 | 3971274 | C | T | synonymous_variant | LOW | c.510C>T|p.Asn170Asn |
S202 |
8 | BAA02g08990 | A02 | 3971960 | G | A | missense_variant | MODERATE | c.1196G>A|p.Gly399Asp |
S184 |
9 | BAA02g08990 | A02 | 3972431 | G | A | downstream_gene_variant | MODIFIER | c.*140G>A| |
S34 |
10 | BAA02g08990 | A02 | 3973094 | G | A | downstream_gene_variant | MODIFIER | c.*803G>A| |
S295 |
11 | BAA02g08990 | A02 | 3973817 | C | T | downstream_gene_variant | MODIFIER | c.*1526C>T| |
S121 |
12 | BAA02g08990 | A02 | 3974727 | C | T | downstream_gene_variant | MODIFIER | c.*2436C>T| |
S136 |
13 | BAA02g08990 | A02 | 3974924 | C | T | downstream_gene_variant | MODIFIER | c.*2633C>T| |
S138 |
14 | BAA02g08990 | A02 | 3975418 | C | T | downstream_gene_variant | MODIFIER | c.*3127C>T| |
S1 S90 |
15 | BAA02g08990 | A02 | 3975640 | G | A | downstream_gene_variant | MODIFIER | c.*3349G>A| |
S133 |
16 | BAA02g08990 | A02 | 3975777 | G | A | downstream_gene_variant | MODIFIER | c.*3486G>A| |
S287 S68 |