Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19550 | A02 | 10156232 | G | A | downstream_gene_variant | MODIFIER | c.*288C>T| |
S263 |
2 | BAA02g19550 | A02 | 10157110 | C | T | missense_variant | MODERATE | c.145G>A|p.Val49Ile |
S301 S304 |
3 | BAA02g19550 | A02 | 10157233 | C | T | missense_variant | MODERATE | c.22G>A|p.Gly8Arg |
S209 |
4 | BAA02g19550 | A02 | 10157503 | G | A | upstream_gene_variant | MODIFIER | c.-249C>T| |
S67 |
5 | BAA02g19550 | A02 | 10157972 | C | T | upstream_gene_variant | MODIFIER | c.-718G>A| |
S216 |
6 | BAA02g19550 | A02 | 10157976 | G | A | upstream_gene_variant | MODIFIER | c.-722C>T| |
S113 |
7 | BAA02g19550 | A02 | 10158125 | G | A | upstream_gene_variant | MODIFIER | c.-871C>T| |
S67 |
8 | BAA02g19550 | A02 | 10159819 | G | A | upstream_gene_variant | MODIFIER | c.-2565C>T| |
S265 |
9 | BAA02g19550 | A02 | 10161323 | G | A | upstream_gene_variant | MODIFIER | c.-4069C>T| |
S217 S248 |