Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44290 | A02 | 36534589 | C | T | upstream_gene_variant | MODIFIER | c.-4263C>T| |
S172 S217 |
2 | BAA02g44290 | A02 | 36534786 | C | T | upstream_gene_variant | MODIFIER | c.-4066C>T| |
S48 |
3 | BAA02g44290 | A02 | 36535393 | C | T | upstream_gene_variant | MODIFIER | c.-3459C>T| |
S117 |
4 | BAA02g44290 | A02 | 36535449 | G | A | upstream_gene_variant | MODIFIER | c.-3403G>A| |
S96 |
5 | BAA02g44290 | A02 | 36535731 | G | A | upstream_gene_variant | MODIFIER | c.-3121G>A| |
S11 |
6 | BAA02g44290 | A02 | 36535736 | C | T | upstream_gene_variant | MODIFIER | c.-3116C>T| |
S201 |
7 | BAA02g44290 | A02 | 36535960 | C | T | upstream_gene_variant | MODIFIER | c.-2892C>T| |
S280 |
8 | BAA02g44290 | A02 | 36536192 | G | A | upstream_gene_variant | MODIFIER | c.-2660G>A| |
S20 |
9 | BAA02g44290 | A02 | 36536495 | G | A | upstream_gene_variant | MODIFIER | c.-2357G>A| |
S60 |
10 | BAA02g44290 | A02 | 36536785 | C | T | upstream_gene_variant | MODIFIER | c.-2067C>T| |
S189 |
11 | BAA02g44290 | A02 | 36536871 | C | T | upstream_gene_variant | MODIFIER | c.-1981C>T| |
S180 |
12 | BAA02g44290 | A02 | 36537955 | G | A | upstream_gene_variant | MODIFIER | c.-897G>A| |
S144 |
13 | BAA02g44290 | A02 | 36538736 | C | T | upstream_gene_variant | MODIFIER | c.-116C>T| |
S64 |
14 | BAA02g44290 | A02 | 36539058 | C | T | synonymous_variant | LOW | c.207C>T|p.Phe69Phe |
S34 |
15 | BAA02g44290 | A02 | 36539765 | G | A | missense_variant | MODERATE | c.914G>A|p.Arg305Gln |
S155 S211 |
16 | BAA02g44290 | A02 | 36540794 | C | T | missense_variant | MODERATE | c.1943C>T|p.Ser648Phe |
S270 |