Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAS13g00200 | Scaffold13 | 4447635 | G | A | upstream_gene_variant | MODIFIER | c.-3725G>A| |
S240 |
2 | BAS13g00200 | Scaffold13 | 4449827 | C | T | upstream_gene_variant | MODIFIER | c.-1533C>T| |
S267 |
3 | BAS13g00200 | Scaffold13 | 4451139 | G | A | upstream_gene_variant | MODIFIER | c.-221G>A| |
S91 |
4 | BAS13g00200 | Scaffold13 | 4452649 | C | T | intron_variant | MODIFIER | c.685-234C>T| |
S249 |
5 | BAS13g00200 | Scaffold13 | 4452765 | G | A | intron_variant | MODIFIER | c.685-118G>A| |
S78 |
6 | BAS13g00200 | Scaffold13 | 4453075 | C | T | missense_variant | MODERATE | c.788C>T|p.Ser263Phe |
S190 |
7 | BAS13g00200 | Scaffold13 | 4453201 | C | T | intron_variant | MODIFIER | c.900+14C>T| |
S138 |
8 | BAS13g00200 | Scaffold13 | 4453423 | C | T | stop_gained | HIGH | c.1012C>T|p.Gln338* |
S278 |
9 | BAS13g00200 | Scaffold13 | 4453517 | G | A | missense_variant | MODERATE | c.1106G>A|p.Ser369Asn |
S142 |
10 | BAS13g00200 | Scaffold13 | 4454439 | G | A | downstream_gene_variant | MODIFIER | c.*243G>A| |
S34 |
11 | BAS13g00200 | Scaffold13 | 4455628 | G | A | downstream_gene_variant | MODIFIER | c.*1432G>A| |
S232 |
12 | BAS13g00200 | Scaffold13 | 4456283 | G | A | downstream_gene_variant | MODIFIER | c.*2087G>A| |
S251 |
13 | BAS13g00200 | Scaffold13 | 4457007 | C | T | downstream_gene_variant | MODIFIER | c.*2811C>T| |
S221 |
14 | BAS13g00200 | Scaffold13 | 4457549 | C | T | downstream_gene_variant | MODIFIER | c.*3353C>T| |
S40 S49 |
15 | BAS13g00200 | Scaffold13 | 4457886 | C | T | downstream_gene_variant | MODIFIER | c.*3690C>T| |
S286 |