Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g34630 | A02 | 29726565 | C | T | upstream_gene_variant | MODIFIER | c.-2271C>T| |
S53 |
2 | BAA02g34630 | A02 | 29729400 | C | T | missense_variant&splice_region_variant | MODERATE | c.185C>T|p.Ala62Val |
S124 |
3 | BAA02g34630 | A02 | 29729560 | G | A | missense_variant | MODERATE | c.229G>A|p.Gly77Arg |
S279 |
4 | BAA02g34630 | A02 | 29729855 | G | A | intron_variant | MODIFIER | c.361+69G>A| |
S11 |
5 | BAA02g34630 | A02 | 29729979 | G | A | intron_variant | MODIFIER | c.361+193G>A| |
S187 |
6 | BAA02g34630 | A02 | 29730624 | C | T | missense_variant | MODERATE | c.397C>T|p.Pro133Ser |
S2 |
7 | BAA02g34630 | A02 | 29731329 | C | T | downstream_gene_variant | MODIFIER | c.*305C>T| |
S68 |
8 | BAA02g34630 | A02 | 29732093 | C | T | downstream_gene_variant | MODIFIER | c.*1069C>T| |
S19 |
9 | BAA02g34630 | A02 | 29733762 | G | A | downstream_gene_variant | MODIFIER | c.*2738G>A| |
S158 |
10 | BAA02g34630 | A02 | 29733783 | C | T | downstream_gene_variant | MODIFIER | c.*2759C>T| |
S177 |
11 | BAA02g34630 | A02 | 29733954 | G | A | downstream_gene_variant | MODIFIER | c.*2930G>A| |
S123 |
12 | BAA02g34630 | A02 | 29734070 | C | T | downstream_gene_variant | MODIFIER | c.*3046C>T| |
S82 S92 |
13 | BAA02g34630 | A02 | 29734116 | G | A | downstream_gene_variant | MODIFIER | c.*3092G>A| |
S251 |
14 | BAA02g34630 | A02 | 29735103 | G | A | downstream_gene_variant | MODIFIER | c.*4079G>A| |
S256 |