Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g24440 | A09 | 15589983 | C | T | upstream_gene_variant | MODIFIER | c.-4246C>T| |
S243 |
2 | BAA09g24440 | A09 | 15590492 | C | T | upstream_gene_variant | MODIFIER | c.-3737C>T| |
S302 |
3 | BAA09g24440 | A09 | 15590772 | G | A | upstream_gene_variant | MODIFIER | c.-3457G>A| |
S55 |
4 | BAA09g24440 | A09 | 15591304 | G | A | upstream_gene_variant | MODIFIER | c.-2925G>A| |
S292 |
5 | BAA09g24440 | A09 | 15592584 | C | T | upstream_gene_variant | MODIFIER | c.-1645C>T| |
S256 |
6 | BAA09g24440 | A09 | 15592988 | G | A | upstream_gene_variant | MODIFIER | c.-1241G>A| |
S249 |
7 | BAA09g24440 | A09 | 15593858 | G | A | upstream_gene_variant | MODIFIER | c.-371G>A| |
S240 |
8 | BAA09g24440 | A09 | 15594123 | C | T | upstream_gene_variant | MODIFIER | c.-106C>T| |
S90 |
9 | BAA09g24440 | A09 | 15595821 | C | T | missense_variant | MODERATE | c.686C>T|p.Ser229Phe |
S239 |
10 | BAA09g24440 | A09 | 15596012 | C | T | stop_gained | HIGH | c.877C>T|p.Gln293* |
S256 |
11 | BAA09g24440 | A09 | 15596471 | G | A | missense_variant | MODERATE | c.1336G>A|p.Gly446Arg |
S204 |
12 | BAA09g24440 | A09 | 15598146 | C | T | downstream_gene_variant | MODIFIER | c.*1661C>T| |
S6 |
13 | BAA09g24440 | A09 | 15598187 | C | T | downstream_gene_variant | MODIFIER | c.*1702C>T| |
S200 |
14 | BAA09g24440 | A09 | 15599825 | C | T | downstream_gene_variant | MODIFIER | c.*3340C>T| |
S82 S92 |
15 | BAA09g24440 | A09 | 15599830 | G | A | downstream_gene_variant | MODIFIER | c.*3345G>A| |
S45 |
16 | BAA09g24440 | A09 | 15601128 | T | A | downstream_gene_variant | MODIFIER | c.*4643T>A| |
S132 S137 |