Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g41590 | A06 | 27091369 | G | A | synonymous_variant | LOW | c.1587C>T|p.Ser529Ser |
S256 |
2 | BAA06g41590 | A06 | 27092301 | C | T | missense_variant | MODERATE | c.1054G>A|p.Ala352Thr |
S308 |
3 | BAA06g41590 | A06 | 27095057 | C | T | upstream_gene_variant | MODIFIER | c.-917G>A| |
S165 |
4 | BAA06g41590 | A06 | 27096702 | G | A | upstream_gene_variant | MODIFIER | c.-2562C>T| |
S13 |
5 | BAA06g41590 | A06 | 27097645 | T | A | upstream_gene_variant | MODIFIER | c.-3505A>T| |
S37 |
6 | BAA06g41590 | A06 | 27098238 | G | A | upstream_gene_variant | MODIFIER | c.-4098C>T| |
S38 |
7 | BAA06g41590 | A06 | 27098987 | C | T | upstream_gene_variant | MODIFIER | c.-4847G>A| |
S104 |