Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g38100 | A02 | 32550363 | C | T | upstream_gene_variant | MODIFIER | c.-4546C>T| |
S46 |
2 | BAA02g38100 | A02 | 32550638 | C | T | upstream_gene_variant | MODIFIER | c.-4271C>T| |
S189 |
3 | BAA02g38100 | A02 | 32553613 | C | T | upstream_gene_variant | MODIFIER | c.-1296C>T| |
S247 |
4 | BAA02g38100 | A02 | 32553773 | C | T | upstream_gene_variant | MODIFIER | c.-1136C>T| |
S308 |
5 | BAA02g38100 | A02 | 32553854 | G | A | upstream_gene_variant | MODIFIER | c.-1055G>A| |
S207 S44 |
6 | BAA02g38100 | A02 | 32554034 | G | A | upstream_gene_variant | MODIFIER | c.-875G>A| |
S217 |
7 | BAA02g38100 | A02 | 32554640 | C | T | upstream_gene_variant | MODIFIER | c.-269C>T| |
S16 |
8 | BAA02g38100 | A02 | 32554809 | C | T | upstream_gene_variant | MODIFIER | c.-100C>T| |
S18 |
9 | BAA02g38100 | A02 | 32555423 | C | T | missense_variant | MODERATE | c.515C>T|p.Ser172Phe |
S15 |
10 | BAA02g38100 | A02 | 32555894 | G | A | missense_variant | MODERATE | c.916G>A|p.Glu306Lys |
S72 S78 |