Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g45590 | A09 | 50758290 | G | A | missense_variant | MODERATE | c.76G>A|p.Ala26Thr |
S134 |
2 | BAA09g45590 | A09 | 50758598 | C | T | synonymous_variant | LOW | c.384C>T|p.Gly128Gly |
S182 |
3 | BAA09g45590 | A09 | 50760267 | G | A | missense_variant | MODERATE | c.1205G>A|p.Gly402Asp |
S44 |
4 | BAA09g45590 | A09 | 50760954 | C | T | missense_variant | MODERATE | c.1546C>T|p.Pro516Ser |
S18 |
5 | BAA09g45590 | A09 | 50764442 | C | T | downstream_gene_variant | MODIFIER | c.*3203C>T| |
S183 S198 |