Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g04620 | A05 | 2228597 | C | T | upstream_gene_variant | MODIFIER | c.-2998C>T| |
S16 |
2 | BAA05g04620 | A05 | 2229239 | G | A | upstream_gene_variant | MODIFIER | c.-2356G>A| |
S32 |
3 | BAA05g04620 | A05 | 2229743 | G | A | upstream_gene_variant | MODIFIER | c.-1852G>A| |
S32 |
4 | BAA05g04620 | A05 | 2229905 | G | A | upstream_gene_variant | MODIFIER | c.-1690G>A| |
S153 |
5 | BAA05g04620 | A05 | 2229984 | G | A | upstream_gene_variant | MODIFIER | c.-1611G>A| |
S32 |
6 | BAA05g04620 | A05 | 2231201 | C | T | upstream_gene_variant | MODIFIER | c.-394C>T| |
S107 |
7 | BAA05g04620 | A05 | 2231348 | C | T | upstream_gene_variant | MODIFIER | c.-247C>T| |
S60 |
8 | BAA05g04620 | A05 | 2231645 | C | T | synonymous_variant | LOW | c.51C>T|p.Ala17Ala |
S265 |
9 | BAA05g04620 | A05 | 2235238 | G | A | missense_variant | MODERATE | c.1321G>A|p.Ala441Thr |
S63 |
10 | BAA05g04620 | A05 | 2235469 | G | A | missense_variant | MODERATE | c.1426G>A|p.Asp476Asn |
S62 |