Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g10860 | A09 | 5985020 | C | T | missense_variant | MODERATE | c.394C>T|p.Pro132Ser |
S232 |
2 | BAA09g10860 | A09 | 5985872 | G | A | synonymous_variant | LOW | c.1086G>A|p.Gly362Gly |
S281 |
3 | BAA09g10860 | A09 | 5986099 | C | T | intron_variant | MODIFIER | c.1228+20C>T| |
S150 |
4 | BAA09g10860 | A09 | 5986558 | G | A | intron_variant | MODIFIER | c.1388-77G>A| |
S274 |