Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02830 | A02 | 1279915 | C | T | missense_variant | MODERATE | c.121C>T|p.Pro41Ser |
S130 |
2 | BAA02g02830 | A02 | 1279976 | C | T | missense_variant | MODERATE | c.182C>T|p.Thr61Ile |
S216 |
3 | BAA02g02830 | A02 | 1280623 | G | A | missense_variant | MODERATE | c.542G>A|p.Gly181Asp |
S43 |
4 | BAA02g02830 | A02 | 1280705 | C | T | splice_region_variant&intron_variant | LOW | c.618+6C>T| |
S249 |
5 | BAA02g02830 | A02 | 1281914 | G | A | downstream_gene_variant | MODIFIER | c.*249G>A| |
S68 |