Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g10970 | A01 | 5052639 | C | T | upstream_gene_variant | MODIFIER | c.-2398C>T| |
S287 |
2 | BAA01g10970 | A01 | 5052935 | G | A | upstream_gene_variant | MODIFIER | c.-2102G>A| |
S28 |
3 | BAA01g10970 | A01 | 5052945 | C | T | upstream_gene_variant | MODIFIER | c.-2092C>T| |
S61 |
4 | BAA01g10970 | A01 | 5052981 | C | T | upstream_gene_variant | MODIFIER | c.-2056C>T| |
S246 |
5 | BAA01g10970 | A01 | 5053794 | C | T | upstream_gene_variant | MODIFIER | c.-1243C>T| |
S1 S90 |
6 | BAA01g10970 | A01 | 5054380 | G | A | upstream_gene_variant | MODIFIER | c.-657G>A| |
S173 |
7 | BAA01g10970 | A01 | 5055179 | C | T | missense_variant | MODERATE | c.143C>T|p.Thr48Met |
S119 |
8 | BAA01g10970 | A01 | 5058224 | G | A | downstream_gene_variant | MODIFIER | c.*2951G>A| |
S293 |
9 | BAA01g10970 | A01 | 5058707 | G | A | downstream_gene_variant | MODIFIER | c.*3434G>A| |
S133 |
10 | BAA01g10970 | A01 | 5059678 | C | T | downstream_gene_variant | MODIFIER | c.*4405C>T| |
S20 |
11 | BAA01g10970 | A01 | 5060176 | G | A | downstream_gene_variant | MODIFIER | c.*4903G>A| |
S153 |