Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g21160 | A01 | 10453417 | C | T | intron_variant | MODIFIER | c.1167+74C>T| |
S295 |
2 | BAA01g21160 | A01 | 10453502 | C | T | intron_variant | MODIFIER | c.1168-36C>T| |
S99 |
3 | BAA01g21160 | A01 | 10454171 | C | T | splice_region_variant&intron_variant | LOW | c.1421-7C>T| |
S184 |
4 | BAA01g21160 | A01 | 10454706 | C | T | synonymous_variant | LOW | c.1767C>T|p.Leu589Leu |
S66 |
5 | BAA01g21160 | A01 | 10454712 | C | T | synonymous_variant | LOW | c.1773C>T|p.Ser591Ser |
S231 |
6 | BAA01g21160 | A01 | 10454830 | G | A | missense_variant | MODERATE | c.1801G>A|p.Val601Ile |
S49 |
7 | BAA01g21160 | A01 | 10456870 | G | A | downstream_gene_variant | MODIFIER | c.*1846G>A| |
S180 |
8 | BAA01g21160 | A01 | 10457460 | G | T | downstream_gene_variant | MODIFIER | c.*2436G>T| |
S181 |