Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g38980 | A02 | 33200659 | C | T | upstream_gene_variant | MODIFIER | c.-4580C>T| |
S234 |
2 | BAA02g38980 | A02 | 33205661 | G | A | missense_variant | MODERATE | c.247G>A|p.Val83Met |
S221 |
3 | BAA02g38980 | A02 | 33206518 | C | T | synonymous_variant | LOW | c.858C>T|p.Asp286Asp |
S107 |
4 | BAA02g38980 | A02 | 33207597 | C | T | splice_region_variant&intron_variant | LOW | c.1569+7C>T| |
S32 |