Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g00980 | A01 | 424416 | C | T | upstream_gene_variant | MODIFIER | c.-985C>T| |
S20 |
2 | BAA01g00980 | A01 | 425175 | C | T | upstream_gene_variant | MODIFIER | c.-226C>T| |
S273 |
3 | BAA01g00980 | A01 | 425420 | C | T | missense_variant | MODERATE | c.20C>T|p.Ala7Val |
S40 S49 |
4 | BAA01g00980 | A01 | 425493 | C | T | synonymous_variant | LOW | c.93C>T|p.Ser31Ser |
S137 |
5 | BAA01g00980 | A01 | 425646 | T | G | synonymous_variant | LOW | c.246T>G|p.Pro82Pro |
S203 |
6 | BAA01g00980 | A01 | 425692 | G | A | missense_variant | MODERATE | c.292G>A|p.Glu98Lys |
S116 |
7 | BAA01g00980 | A01 | 425778 | C | T | synonymous_variant | LOW | c.378C>T|p.Leu126Leu |
S62 |
8 | BAA01g00980 | A01 | 426266 | G | A | splice_region_variant&intron_variant | LOW | c.782+5G>A| |
S260 |
9 | BAA01g00980 | A01 | 429375 | G | A | downstream_gene_variant | MODIFIER | c.*2046G>A| |
S295 |