Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g39960 | A02 | 33790881 | G | A | stop_gained | HIGH | c.1720C>T|p.Gln574* |
|
2 | BAA02g39960 | A02 | 33790927 | C | T | synonymous_variant | LOW | c.1674G>A|p.Gln558Gln |
S100 |
3 | BAA02g39960 | A02 | 33791189 | C | T | missense_variant | MODERATE | c.1412G>A|p.Arg471His |
S261 |
4 | BAA02g39960 | A02 | 33791657 | G | A | missense_variant | MODERATE | c.944C>T|p.Ser315Phe |
S232 |
5 | BAA02g39960 | A02 | 33791830 | C | T | synonymous_variant | LOW | c.771G>A|p.Gly257Gly |
S295 |
6 | BAA02g39960 | A02 | 33792559 | G | A | synonymous_variant | LOW | c.384C>T|p.Ser128Ser |
S221 |
7 | BAA02g39960 | A02 | 33792816 | C | T | missense_variant | MODERATE | c.127G>A|p.Asp43Asn |
S250 |
8 | BAA02g39960 | A02 | 33793607 | G | A | upstream_gene_variant | MODIFIER | c.-665C>T| |
S71 |
9 | BAA02g39960 | A02 | 33794366 | C | T | upstream_gene_variant | MODIFIER | c.-1424G>A| |
S244 |