Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g41270 | A01 | 27435573 | G | A | missense_variant | MODERATE | c.665G>A|p.Ser222Asn |
S236 |
2 | BAA01g41270 | A01 | 27435582 | G | A | missense_variant | MODERATE | c.674G>A|p.Gly225Glu |
S212 |
3 | BAA01g41270 | A01 | 27435801 | C | T | missense_variant | MODERATE | c.893C>T|p.Pro298Leu |
S294 |
4 | BAA01g41270 | A01 | 27435853 | C | T | synonymous_variant | LOW | c.945C>T|p.Leu315Leu |
S286 |
5 | BAA01g41270 | A01 | 27438840 | C | T | downstream_gene_variant | MODIFIER | c.*2954C>T| |
S153 |
6 | BAA01g41270 | A01 | 27438860 | C | T | downstream_gene_variant | MODIFIER | c.*2974C>T| |
S208 S93 |
7 | BAA01g41270 | A01 | 27439092 | C | T | downstream_gene_variant | MODIFIER | c.*3206C>T| |
S97 |
8 | BAA01g41270 | A01 | 27440417 | G | A | downstream_gene_variant | MODIFIER | c.*4531G>A| |
S197 |
9 | BAA01g41270 | A01 | 27440483 | G | A | downstream_gene_variant | MODIFIER | c.*4597G>A| |
S197 |