Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g44600 | A01 | 29693546 | G | A | upstream_gene_variant | MODIFIER | c.-4133G>A| |
S208 S219 |
2 | BAA01g44600 | A01 | 29693551 | C | T | upstream_gene_variant | MODIFIER | c.-4128C>T| |
S37 |
3 | BAA01g44600 | A01 | 29697331 | G | A | upstream_gene_variant | MODIFIER | c.-348G>A| |
S53 |
4 | BAA01g44600 | A01 | 29697612 | C | T | upstream_gene_variant | MODIFIER | c.-67C>T| |
S259 |
5 | BAA01g44600 | A01 | 29697758 | C | T | missense_variant&splice_region_variant | MODERATE | c.80C>T|p.Ser27Phe |
S47 |
6 | BAA01g44600 | A01 | 29699181 | C | T | missense_variant | MODERATE | c.976C>T|p.Leu326Phe |
S32 |
7 | BAA01g44600 | A01 | 29699416 | G | A | missense_variant | MODERATE | c.1141G>A|p.Val381Ile |
S106 S185 |
8 | BAA01g44600 | A01 | 29699795 | C | T | synonymous_variant | LOW | c.1363C>T|p.Leu455Leu |
S48 |