Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g27890 | A01 | 16953638 | C | T | upstream_gene_variant | MODIFIER | c.-4369C>T| |
S200 |
2 | BAA01g27890 | A01 | 16953843 | G | A | upstream_gene_variant | MODIFIER | c.-4164G>A| |
S221 |
3 | BAA01g27890 | A01 | 16954571 | G | A | upstream_gene_variant | MODIFIER | c.-3436G>A| |
S207 |
4 | BAA01g27890 | A01 | 16954823 | G | A | upstream_gene_variant | MODIFIER | c.-3184G>A| |
S188 |
5 | BAA01g27890 | A01 | 16954984 | C | T | upstream_gene_variant | MODIFIER | c.-3023C>T| |
S82 S92 |
6 | BAA01g27890 | A01 | 16956589 | T | A | upstream_gene_variant | MODIFIER | c.-1418T>A| |
S249 |
7 | BAA01g27890 | A01 | 16956842 | C | T | upstream_gene_variant | MODIFIER | c.-1165C>T| |
S142 |
8 | BAA01g27890 | A01 | 16956958 | C | T | upstream_gene_variant | MODIFIER | c.-1049C>T| |
S192 |
9 | BAA01g27890 | A01 | 16958217 | G | A | missense_variant | MODERATE | c.211G>A|p.Ala71Thr |
S70 |
10 | BAA01g27890 | A01 | 16958696 | G | A | downstream_gene_variant | MODIFIER | c.*32G>A| |
S298 |
11 | BAA01g27890 | A01 | 16959594 | C | T | downstream_gene_variant | MODIFIER | c.*930C>T| |
S54 |
12 | BAA01g27890 | A01 | 16959921 | G | A | downstream_gene_variant | MODIFIER | c.*1257G>A| |
S14 S224 |
13 | BAA01g27890 | A01 | 16959972 | G | A | downstream_gene_variant | MODIFIER | c.*1308G>A| |
S292 |