Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g16110 | A10 | 16104977 | C | T | missense_variant | MODERATE | c.94C>T|p.Leu32Phe |
S152 |
2 | BAA10g16110 | A10 | 16105048 | C | T | splice_region_variant&intron_variant | LOW | c.162+3C>T| |
S168 |
3 | BAA10g16110 | A10 | 16105130 | C | T | missense_variant | MODERATE | c.173C>T|p.Ala58Val |
S259 |
4 | BAA10g16110 | A10 | 16105139 | C | T | missense_variant | MODERATE | c.182C>T|p.Ser61Phe |
S8 |