Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g00160 | A01 | 81610 | G | A | downstream_gene_variant | MODIFIER | c.*4884C>T| |
S161 |
2 | BAA01g00160 | A01 | 82487 | C | T | downstream_gene_variant | MODIFIER | c.*4007G>A| |
S16 |
3 | BAA01g00160 | A01 | 83966 | C | T | downstream_gene_variant | MODIFIER | c.*2528G>A| |
S66 |
4 | BAA01g00160 | A01 | 84294 | G | A | downstream_gene_variant | MODIFIER | c.*2200C>T| |
S152 |
5 | BAA01g00160 | A01 | 84552 | C | T | downstream_gene_variant | MODIFIER | c.*1942G>A| |
S164 |
6 | BAA01g00160 | A01 | 84941 | G | A | downstream_gene_variant | MODIFIER | c.*1553C>T| |
S283 |
7 | BAA01g00160 | A01 | 85042 | G | A | downstream_gene_variant | MODIFIER | c.*1452C>T| |
S133 |
8 | BAA01g00160 | A01 | 85260 | C | T | downstream_gene_variant | MODIFIER | c.*1234G>A| |
S282 |
9 | BAA01g00160 | A01 | 86029 | G | A | downstream_gene_variant | MODIFIER | c.*465C>T| |
S256 |
10 | BAA01g00160 | A01 | 86034 | C | T | downstream_gene_variant | MODIFIER | c.*460G>A| |
S284 |
11 | BAA01g00160 | A01 | 86417 | G | A | downstream_gene_variant | MODIFIER | c.*77C>T| |
S228 |
12 | BAA01g00160 | A01 | 88316 | C | T | upstream_gene_variant | MODIFIER | c.-1289G>A| |
S205 |
13 | BAA01g00160 | A01 | 88396 | C | T | upstream_gene_variant | MODIFIER | c.-1369G>A| |
S205 |
14 | BAA01g00160 | A01 | 88407 | G | A | upstream_gene_variant | MODIFIER | c.-1380C>T| |
S172 |
15 | BAA01g00160 | A01 | 88665 | G | A | upstream_gene_variant | MODIFIER | c.-1638C>T| |
S201 |
16 | BAA01g00160 | A01 | 89808 | C | T | upstream_gene_variant | MODIFIER | c.-2781G>A| |
S269 |
17 | BAA01g00160 | A01 | 89877 | C | T | upstream_gene_variant | MODIFIER | c.-2850G>A| |
S192 |