Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g18400 | A05 | 10525892 | G | A | downstream_gene_variant | MODIFIER | c.*4914C>T| |
S179 |
2 | BAA05g18400 | A05 | 10527032 | C | A | downstream_gene_variant | MODIFIER | c.*3774G>T| |
S190 |
3 | BAA05g18400 | A05 | 10527141 | C | T | downstream_gene_variant | MODIFIER | c.*3665G>A| |
S167 |
4 | BAA05g18400 | A05 | 10527477 | C | T | downstream_gene_variant | MODIFIER | c.*3329G>A| |
S295 |
5 | BAA05g18400 | A05 | 10527918 | C | T | downstream_gene_variant | MODIFIER | c.*2888G>A| |
S237 |
6 | BAA05g18400 | A05 | 10528900 | C | T | downstream_gene_variant | MODIFIER | c.*1906G>A| |
S195 S9 |
7 | BAA05g18400 | A05 | 10529420 | G | A | downstream_gene_variant | MODIFIER | c.*1386C>T| |
S178 |
8 | BAA05g18400 | A05 | 10529695 | G | A | downstream_gene_variant | MODIFIER | c.*1111C>T| |
S38 |
9 | BAA05g18400 | A05 | 10529867 | C | T | downstream_gene_variant | MODIFIER | c.*939G>A| |
S305 |
10 | BAA05g18400 | A05 | 10531223 | G | A | synonymous_variant | LOW | c.870C>T|p.Ser290Ser |
S111 |
11 | BAA05g18400 | A05 | 10531324 | G | A | missense_variant | MODERATE | c.769C>T|p.Leu257Phe |
S10 |
12 | BAA05g18400 | A05 | 10531452 | G | A | missense_variant | MODERATE | c.641C>T|p.Ser214Leu |
S293 |
13 | BAA05g18400 | A05 | 10531587 | C | T | missense_variant | MODERATE | c.506G>A|p.Gly169Glu |
S83 S88 |
14 | BAA05g18400 | A05 | 10535545 | G | A | upstream_gene_variant | MODIFIER | c.-3453C>T| |
S282 |
15 | BAA05g18400 | A05 | 10537011 | G | A | upstream_gene_variant | MODIFIER | c.-4919C>T| |
S46 |