Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g37290 | A02 | 31992981 | C | T | missense_variant | MODERATE | c.124G>A|p.Ala42Thr |
S120 |
2 | BAA02g37290 | A02 | 31993052 | G | A | missense_variant | MODERATE | c.53C>T|p.Ser18Phe |
S110 |
3 | BAA02g37290 | A02 | 31993473 | C | T | upstream_gene_variant | MODIFIER | c.-369G>A| |
S274 |
4 | BAA02g37290 | A02 | 31995133 | G | A | upstream_gene_variant | MODIFIER | c.-2029C>T| |
S37 |
5 | BAA02g37290 | A02 | 31995200 | C | T | upstream_gene_variant | MODIFIER | c.-2096G>A| |
S15 S156 S3 S34 |
6 | BAA02g37290 | A02 | 31995870 | G | A | upstream_gene_variant | MODIFIER | c.-2766C>T| |
S238 |