Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAS61g00080 | Scaffold61 | 3227913 | G | A | missense_variant | MODERATE | c.1325C>T|p.Thr442Ile |
S144 |
2 | BAS61g00080 | Scaffold61 | 3228826 | G | A | synonymous_variant | LOW | c.486C>T|p.Arg162Arg |
S277 |
3 | BAS61g00080 | Scaffold61 | 3229458 | C | T | synonymous_variant | LOW | c.153G>A|p.Thr51Thr |
S221 |
4 | BAS61g00080 | Scaffold61 | 3229578 | C | T | synonymous_variant | LOW | c.33G>A|p.Lys11Lys |
S186 |
5 | BAS61g00080 | Scaffold61 | 3229732 | G | T | upstream_gene_variant | MODIFIER | c.-122C>A| |
S44 |
6 | BAS61g00080 | Scaffold61 | 3232007 | C | T | upstream_gene_variant | MODIFIER | c.-2397G>A| |
S37 |
7 | BAS61g00080 | Scaffold61 | 3232030 | C | T | upstream_gene_variant | MODIFIER | c.-2420G>A| |
S260 |
8 | BAS61g00080 | Scaffold61 | 3232045 | G | A | upstream_gene_variant | MODIFIER | c.-2435C>T| |
S162 |
9 | BAS61g00080 | Scaffold61 | 3232166 | C | T | upstream_gene_variant | MODIFIER | c.-2556G>A| |
S298 |
10 | BAS61g00080 | Scaffold61 | 3232681 | C | T | upstream_gene_variant | MODIFIER | c.-3071G>A| |
S249 |