Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g40380 | A01 | 26777719 | C | T | missense_variant | MODERATE | c.1777G>A|p.Glu593Lys |
S216 |
2 | BAA01g40380 | A01 | 26777930 | G | A | synonymous_variant | LOW | c.1566C>T|p.Phe522Phe |
S117 |
3 | BAA01g40380 | A01 | 26779374 | C | T | missense_variant&splice_region_variant | MODERATE | c.346G>A|p.Val116Ile |
S78 |
4 | BAA01g40380 | A01 | 26780073 | C | T | splice_region_variant&intron_variant | LOW | c.50-6G>A| |
S204 |
5 | BAA01g40380 | A01 | 26781534 | C | T | upstream_gene_variant | MODIFIER | c.-1033G>A| |
S264 |
6 | BAA01g40380 | A01 | 26784213 | C | T | upstream_gene_variant | MODIFIER | c.-3712G>A| |
S266 |