Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g50460 | A09 | 53323097 | C | T | synonymous_variant | LOW | c.264C>T|p.Leu88Leu |
S87 |
2 | BAA09g50460 | A09 | 53324455 | C | T | missense_variant | MODERATE | c.722C>T|p.Thr241Ile |
S179 |
3 | BAA09g50460 | A09 | 53324585 | G | A | synonymous_variant | LOW | c.852G>A|p.Glu284Glu |
S262 |
4 | BAA09g50460 | A09 | 53324734 | G | A | missense_variant | MODERATE | c.1001G>A|p.Gly334Asp |
S98 |
5 | BAA09g50460 | A09 | 53324887 | C | T | missense_variant | MODERATE | c.1034C>T|p.Ser345Phe |
S306 |
6 | BAA09g50460 | A09 | 53328554 | C | T | downstream_gene_variant | MODIFIER | c.*2283C>T| |
S53 |