Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g26400 | A01 | 14694383 | G | A | upstream_gene_variant | MODIFIER | c.-1287G>A| |
S92 |
2 | BAA01g26400 | A01 | 14694879 | C | T | upstream_gene_variant | MODIFIER | c.-791C>T| |
S213 |
3 | BAA01g26400 | A01 | 14694943 | C | T | upstream_gene_variant | MODIFIER | c.-727C>T| |
S303 |
4 | BAA01g26400 | A01 | 14695026 | G | A | upstream_gene_variant | MODIFIER | c.-644G>A| |
S138 |
5 | BAA01g26400 | A01 | 14695186 | C | T | upstream_gene_variant | MODIFIER | c.-484C>T| |
S179 |
6 | BAA01g26400 | A01 | 14696527 | A | C | missense_variant | MODERATE | c.596A>C|p.Lys199Thr |
S155 S160 S181 S194 S272 S294 S39 |
7 | BAA01g26400 | A01 | 14696564 | C | T | downstream_gene_variant | MODIFIER | c.*12C>T| |
S107 |
8 | BAA01g26400 | A01 | 14698000 | G | A | downstream_gene_variant | MODIFIER | c.*1448G>A| |
S251 |
9 | BAA01g26400 | A01 | 14698864 | T | A | downstream_gene_variant | MODIFIER | c.*2312T>A| |
S69 |
10 | BAA01g26400 | A01 | 14699107 | C | T | downstream_gene_variant | MODIFIER | c.*2555C>T| |
S277 |
11 | BAA01g26400 | A01 | 14699350 | G | A | downstream_gene_variant | MODIFIER | c.*2798G>A| |
S129 |
12 | BAA01g26400 | A01 | 14699835 | C | T | downstream_gene_variant | MODIFIER | c.*3283C>T| |
S286 |
13 | BAA01g26400 | A01 | 14700601 | C | T | downstream_gene_variant | MODIFIER | c.*4049C>T| |
S53 |