Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g13990 | A02 | 6573578 | C | T | missense_variant | MODERATE | c.520G>A|p.Asp174Asn |
S25 |
2 | BAA02g13990 | A02 | 6575503 | G | A | upstream_gene_variant | MODIFIER | c.-1406C>T| |
S41 |
3 | BAA02g13990 | A02 | 6575519 | G | A | upstream_gene_variant | MODIFIER | c.-1422C>T| |
S272 |
4 | BAA02g13990 | A02 | 6577111 | G | A | upstream_gene_variant | MODIFIER | c.-3014C>T| |
S231 |
5 | BAA02g13990 | A02 | 6577124 | T | G | upstream_gene_variant | MODIFIER | c.-3027A>C| |
S171 S200 S282 S289 |
6 | BAA02g13990 | A02 | 6577133 | G | A | upstream_gene_variant | MODIFIER | c.-3036C>T| |
S13 S157 S168 S279 S64 |