Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01630 | A02 | 725520 | C | T | splice_region_variant&synonymous_variant | LOW | c.6C>T|p.Val2Val |
S47 |
2 | BAA02g01630 | A02 | 726317 | G | A | missense_variant | MODERATE | c.539G>A|p.Gly180Glu |
S244 |
3 | BAA02g01630 | A02 | 726576 | C | T | missense_variant | MODERATE | c.703C>T|p.Pro235Ser |
S257 |