Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g45440 | A01 | 30301994 | G | A | synonymous_variant | LOW | c.231G>A|p.Lys77Lys |
S122 |
2 | BAA01g45440 | A01 | 30301997 | G | A | synonymous_variant | LOW | c.234G>A|p.Arg78Arg |
S262 |
3 | BAA01g45440 | A01 | 30302029 | C | T | missense_variant | MODERATE | c.266C>T|p.Pro89Leu |
S231 |
4 | BAA01g45440 | A01 | 30302783 | G | A | missense_variant | MODERATE | c.562G>A|p.Gly188Arg |
S129 |
5 | BAA01g45440 | A01 | 30303010 | C | T | synonymous_variant | LOW | c.621C>T|p.Ile207Ile |
S42 |
6 | BAA01g45440 | A01 | 30303431 | C | T | missense_variant | MODERATE | c.928C>T|p.His310Tyr |
S8 |
7 | BAA01g45440 | A01 | 30303461 | G | A | missense_variant | MODERATE | c.958G>A|p.Gly320Arg |
S293 |
8 | BAA01g45440 | A01 | 30308151 | C | T | downstream_gene_variant | MODIFIER | c.*4365C>T| |
S37 |
9 | BAA01g45440 | A01 | 30308525 | C | T | downstream_gene_variant | MODIFIER | c.*4739C>T| |
S274 |