Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g13120 | A02 | 5900463 | C | T | upstream_gene_variant | MODIFIER | c.-3785C>T| |
S302 |
2 | BAA02g13120 | A02 | 5900639 | C | T | upstream_gene_variant | MODIFIER | c.-3609C>T| |
S70 |
3 | BAA02g13120 | A02 | 5901279 | G | A | upstream_gene_variant | MODIFIER | c.-2969G>A| |
S213 |
4 | BAA02g13120 | A02 | 5901449 | G | A | upstream_gene_variant | MODIFIER | c.-2799G>A| |
S162 |
5 | BAA02g13120 | A02 | 5901987 | G | A | upstream_gene_variant | MODIFIER | c.-2261G>A| |
S302 |
6 | BAA02g13120 | A02 | 5902500 | C | T | upstream_gene_variant | MODIFIER | c.-1748C>T| |
S261 |
7 | BAA02g13120 | A02 | 5904044 | G | A | upstream_gene_variant | MODIFIER | c.-204G>A| |
S153 S213 |
8 | BAA02g13120 | A02 | 5905100 | G | A | missense_variant | MODERATE | c.389G>A|p.Arg130His |
S166 |
9 | BAA02g13120 | A02 | 5905364 | C | T | missense_variant | MODERATE | c.653C>T|p.Ala218Val |
S206 S26 |
10 | BAA02g13120 | A02 | 5906218 | C | T | missense_variant | MODERATE | c.1262C>T|p.Thr421Ile |
S120 |
11 | BAA02g13120 | A02 | 5906863 | G | A | missense_variant | MODERATE | c.1825G>A|p.Ala609Thr |
S36 |
12 | BAA02g13120 | A02 | 5907398 | G | A | downstream_gene_variant | MODIFIER | c.*482G>A| |
S17 |
13 | BAA02g13120 | A02 | 5907660 | G | A | downstream_gene_variant | MODIFIER | c.*744G>A| |
S68 |
14 | BAA02g13120 | A02 | 5907939 | G | A | downstream_gene_variant | MODIFIER | c.*1023G>A| |
S106 |
15 | BAA02g13120 | A02 | 5908276 | G | A | downstream_gene_variant | MODIFIER | c.*1360G>A| |
S187 |
16 | BAA02g13120 | A02 | 5908733 | G | A | downstream_gene_variant | MODIFIER | c.*1817G>A| |
S268 |
17 | BAA02g13120 | A02 | 5910447 | C | T | downstream_gene_variant | MODIFIER | c.*3531C>T| |
S120 |
18 | BAA02g13120 | A02 | 5911527 | G | A | downstream_gene_variant | MODIFIER | c.*4611G>A| |
S50 |