Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAS13g02950 | Scaffold13 | 24179232 | C | T | downstream_gene_variant | MODIFIER | c.*2413G>A| |
S223 |
2 | BAS13g02950 | Scaffold13 | 24179315 | C | T | downstream_gene_variant | MODIFIER | c.*2330G>A| |
S116 |
3 | BAS13g02950 | Scaffold13 | 24179318 | C | T | downstream_gene_variant | MODIFIER | c.*2327G>A| |
S263 |
4 | BAS13g02950 | Scaffold13 | 24179431 | G | A | downstream_gene_variant | MODIFIER | c.*2214C>T| |
S15 S156 S3 S34 S6 |
5 | BAS13g02950 | Scaffold13 | 24179735 | G | A | downstream_gene_variant | MODIFIER | c.*1910C>T| |
S76 |
6 | BAS13g02950 | Scaffold13 | 24179868 | G | A | downstream_gene_variant | MODIFIER | c.*1777C>T| |
S197 |
7 | BAS13g02950 | Scaffold13 | 24181680 | C | T | missense_variant | MODERATE | c.544G>A|p.Glu182Lys |
S75 S81 |
8 | BAS13g02950 | Scaffold13 | 24181725 | G | A | missense_variant | MODERATE | c.499C>T|p.Leu167Phe |
S110 |
9 | BAS13g02950 | Scaffold13 | 24183384 | G | A | synonymous_variant | LOW | c.114C>T|p.Ala38Ala |
S302 |
10 | BAS13g02950 | Scaffold13 | 24183396 | G | A | synonymous_variant | LOW | c.102C>T|p.Phe34Phe |
S4 |
11 | BAS13g02950 | Scaffold13 | 24184404 | G | A | upstream_gene_variant | MODIFIER | c.-907C>T| |
S162 |