Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g36850 | A01 | 24630481 | C | T | missense_variant | MODERATE | c.41C>T|p.Ser14Phe |
S42 |
2 | BAA01g36850 | A01 | 24630734 | G | A | synonymous_variant | LOW | c.294G>A|p.Thr98Thr |
S245 |
3 | BAA01g36850 | A01 | 24630739 | C | T | missense_variant | MODERATE | c.299C>T|p.Ser100Phe |
S104 S52 |
4 | BAA01g36850 | A01 | 24631667 | C | T | missense_variant | MODERATE | c.670C>T|p.Arg224Cys |
S38 |
5 | BAA01g36850 | A01 | 24631789 | G | A | synonymous_variant | LOW | c.792G>A|p.Arg264Arg |
S140 |
6 | BAA01g36850 | A01 | 24632890 | C | T | missense_variant | MODERATE | c.1811C>T|p.Thr604Ile |
S47 |
7 | BAA01g36850 | A01 | 24636957 | C | T | downstream_gene_variant | MODIFIER | c.*514C>T| |
S74 |
8 | BAA01g36850 | A01 | 24637448 | C | T | downstream_gene_variant | MODIFIER | c.*1005C>T| |
S256 |