Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g02940 | A01 | 1350700 | C | T | missense_variant | MODERATE | c.775G>A|p.Val259Met |
S212 |
2 | BAA01g02940 | A01 | 1351053 | C | T | missense_variant | MODERATE | c.514G>A|p.Asp172Asn |
S72 |
3 | BAA01g02940 | A01 | 1351201 | C | T | splice_region_variant&intron_variant | LOW | c.497+4G>A| |
S185 |
4 | BAA01g02940 | A01 | 1353020 | C | T | upstream_gene_variant | MODIFIER | c.-879G>A| |
S117 |
5 | BAA01g02940 | A01 | 1356400 | C | T | upstream_gene_variant | MODIFIER | c.-4259G>A| |
S81 |
6 | BAA01g02940 | A01 | 1356547 | G | A | upstream_gene_variant | MODIFIER | c.-4406C>T| |
S298 |