Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g28940 | A02 | 16373296 | G | A | upstream_gene_variant | MODIFIER | c.-4779G>A| |
S209 |
2 | BAA02g28940 | A02 | 16373739 | C | T | upstream_gene_variant | MODIFIER | c.-4336C>T| |
S8 |
3 | BAA02g28940 | A02 | 16374016 | C | T | upstream_gene_variant | MODIFIER | c.-4059C>T| |
S287 |
4 | BAA02g28940 | A02 | 16375476 | G | A | upstream_gene_variant | MODIFIER | c.-2599G>A| |
S169 |
5 | BAA02g28940 | A02 | 16376259 | G | A | upstream_gene_variant | MODIFIER | c.-1816G>A| |
S269 |
6 | BAA02g28940 | A02 | 16376744 | C | T | upstream_gene_variant | MODIFIER | c.-1331C>T| |
S178 |
7 | BAA02g28940 | A02 | 16377080 | G | A | upstream_gene_variant | MODIFIER | c.-995G>A| |
S59 |
8 | BAA02g28940 | A02 | 16377241 | C | T | upstream_gene_variant | MODIFIER | c.-834C>T| |
S283 |
9 | BAA02g28940 | A02 | 16377698 | G | A | upstream_gene_variant | MODIFIER | c.-377G>A| |
S127 |
10 | BAA02g28940 | A02 | 16377704 | C | T | upstream_gene_variant | MODIFIER | c.-371C>T| |
S107 |
11 | BAA02g28940 | A02 | 16377798 | C | T | upstream_gene_variant | MODIFIER | c.-277C>T| |
S270 |
12 | BAA02g28940 | A02 | 16378787 | T | G | intron_variant | MODIFIER | c.185+528T>G| |
S164 |
13 | BAA02g28940 | A02 | 16380499 | G | A | missense_variant | MODERATE | c.730G>A|p.Gly244Arg |
S36 |
14 | BAA02g28940 | A02 | 16382455 | C | T | downstream_gene_variant | MODIFIER | c.*1452C>T| |
S179 |
15 | BAA02g28940 | A02 | 16383055 | C | T | downstream_gene_variant | MODIFIER | c.*2052C>T| |
S112 |
16 | BAA02g28940 | A02 | 16383546 | G | A | downstream_gene_variant | MODIFIER | c.*2543G>A| |
S47 |
17 | BAA02g28940 | A02 | 16384397 | G | A | downstream_gene_variant | MODIFIER | c.*3394G>A| |
S292 |
18 | BAA02g28940 | A02 | 16385768 | C | T | downstream_gene_variant | MODIFIER | c.*4765C>T| |
S182 |