Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g20940 | A09 | 12974322 | G | A | downstream_gene_variant | MODIFIER | c.*2722C>T| |
S15 |
2 | BAA09g20940 | A09 | 12974427 | G | A | downstream_gene_variant | MODIFIER | c.*2617C>T| |
S100 |
3 | BAA09g20940 | A09 | 12975003 | C | T | downstream_gene_variant | MODIFIER | c.*2041G>A| |
S174 |
4 | BAA09g20940 | A09 | 12975718 | T | G | downstream_gene_variant | MODIFIER | c.*1326A>C| |
S173 |
5 | BAA09g20940 | A09 | 12975901 | C | T | downstream_gene_variant | MODIFIER | c.*1143G>A| |
S133 |
6 | BAA09g20940 | A09 | 12976849 | C | T | downstream_gene_variant | MODIFIER | c.*195G>A| |
S281 |
7 | BAA09g20940 | A09 | 12977478 | C | T | missense_variant | MODERATE | c.1132G>A|p.Gly378Arg |
S171 |
8 | BAA09g20940 | A09 | 12977541 | G | A | missense_variant | MODERATE | c.1069C>T|p.Pro357Ser |
S80 |
9 | BAA09g20940 | A09 | 12978377 | G | A | missense_variant | MODERATE | c.368C>T|p.Ala123Val |
S251 |
10 | BAA09g20940 | A09 | 12979583 | G | A | upstream_gene_variant | MODIFIER | c.-839C>T| |
S288 |
11 | BAA09g20940 | A09 | 12979773 | C | T | upstream_gene_variant | MODIFIER | c.-1029G>A| |
S48 |