Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g27950 | A01 | 17030990 | C | T | upstream_gene_variant | MODIFIER | c.-4971C>T| |
S142 |
2 | BAA01g27950 | A01 | 17031291 | C | T | upstream_gene_variant | MODIFIER | c.-4670C>T| |
S289 S290 |
3 | BAA01g27950 | A01 | 17032370 | A | T | upstream_gene_variant | MODIFIER | c.-3591A>T| |
S81 |
4 | BAA01g27950 | A01 | 17033437 | G | A | upstream_gene_variant | MODIFIER | c.-2524G>A| |
S163 |
5 | BAA01g27950 | A01 | 17033777 | C | T | upstream_gene_variant | MODIFIER | c.-2184C>T| |
S198 |
6 | BAA01g27950 | A01 | 17034074 | C | T | upstream_gene_variant | MODIFIER | c.-1887C>T| |
S205 |
7 | BAA01g27950 | A01 | 17036755 | G | A | missense_variant | MODERATE | c.202G>A|p.Ala68Thr |
S208 |
8 | BAA01g27950 | A01 | 17036941 | G | A | missense_variant | MODERATE | c.388G>A|p.Val130Ile |
S280 |
9 | BAA01g27950 | A01 | 17036949 | G | A | synonymous_variant | LOW | c.396G>A|p.Leu132Leu |
S208 S93 |