Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g22070 | A01 | 11005120 | C | T | missense_variant | MODERATE | c.2174G>A|p.Gly725Asp |
S43 |
2 | BAA01g22070 | A01 | 11006042 | C | T | missense_variant | MODERATE | c.1318G>A|p.Val440Ile |
S148 S210 S30 S31 |
3 | BAA01g22070 | A01 | 11006484 | C | T | synonymous_variant | LOW | c.876G>A|p.Val292Val |
S158 |
4 | BAA01g22070 | A01 | 11007400 | C | T | upstream_gene_variant | MODIFIER | c.-41G>A| |
S139 |
5 | BAA01g22070 | A01 | 11008496 | G | A | upstream_gene_variant | MODIFIER | c.-1137C>T| |
S72 S78 |
6 | BAA01g22070 | A01 | 11009274 | C | T | upstream_gene_variant | MODIFIER | c.-1915G>A| |
S206 S26 |
7 | BAA01g22070 | A01 | 11010955 | G | A | upstream_gene_variant | MODIFIER | c.-3596C>T| |
S294 |