Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g18500 | A01 | 9075442 | C | T | downstream_gene_variant | MODIFIER | c.*4896G>A| |
S11 |
2 | BAA01g18500 | A01 | 9075560 | C | T | downstream_gene_variant | MODIFIER | c.*4778G>A| |
S39 |
3 | BAA01g18500 | A01 | 9076583 | C | T | downstream_gene_variant | MODIFIER | c.*3755G>A| |
S26 |
4 | BAA01g18500 | A01 | 9076881 | G | A | downstream_gene_variant | MODIFIER | c.*3457C>T| |
S14 S224 |
5 | BAA01g18500 | A01 | 9077733 | G | A | downstream_gene_variant | MODIFIER | c.*2605C>T| |
S138 |
6 | BAA01g18500 | A01 | 9077809 | C | T | downstream_gene_variant | MODIFIER | c.*2529G>A| |
S167 |
7 | BAA01g18500 | A01 | 9078054 | C | T | downstream_gene_variant | MODIFIER | c.*2284G>A| |
S40 S49 |
8 | BAA01g18500 | A01 | 9078227 | G | A | downstream_gene_variant | MODIFIER | c.*2111C>T| |
S71 |
9 | BAA01g18500 | A01 | 9078439 | G | A | downstream_gene_variant | MODIFIER | c.*1899C>T| |
S294 |
10 | BAA01g18500 | A01 | 9078602 | G | A | downstream_gene_variant | MODIFIER | c.*1736C>T| |
S172 S217 |
11 | BAA01g18500 | A01 | 9080269 | C | T | downstream_gene_variant | MODIFIER | c.*69G>A| |
S286 |
12 | BAA01g18500 | A01 | 9080802 | C | T | missense_variant | MODERATE | c.485G>A|p.Gly162Asp |
S255 |
13 | BAA01g18500 | A01 | 9082677 | G | A | upstream_gene_variant | MODIFIER | c.-785C>T| |
S87 |