Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g22950 | A02 | 12471836 | G | A | upstream_gene_variant | MODIFIER | c.-4319G>A| |
S143 |
2 | BAA02g22950 | A02 | 12473026 | C | T | upstream_gene_variant | MODIFIER | c.-3129C>T| |
S97 |
3 | BAA02g22950 | A02 | 12473113 | G | A | upstream_gene_variant | MODIFIER | c.-3042G>A| |
S92 |
4 | BAA02g22950 | A02 | 12473203 | C | T | upstream_gene_variant | MODIFIER | c.-2952C>T| |
S183 S198 S255 |
5 | BAA02g22950 | A02 | 12473277 | G | A | upstream_gene_variant | MODIFIER | c.-2878G>A| |
S69 |
6 | BAA02g22950 | A02 | 12473670 | C | T | upstream_gene_variant | MODIFIER | c.-2485C>T| |
S116 |
7 | BAA02g22950 | A02 | 12474656 | G | A | upstream_gene_variant | MODIFIER | c.-1499G>A| |
S150 |
8 | BAA02g22950 | A02 | 12474714 | C | T | upstream_gene_variant | MODIFIER | c.-1441C>T| |
S32 |
9 | BAA02g22950 | A02 | 12475114 | G | A | upstream_gene_variant | MODIFIER | c.-1041G>A| |
S35 |
10 | BAA02g22950 | A02 | 12476065 | C | T | upstream_gene_variant | MODIFIER | c.-90C>T| |
S242 |
11 | BAA02g22950 | A02 | 12477389 | G | A | missense_variant | MODERATE | c.256G>A|p.Gly86Arg |
S4 |
12 | BAA02g22950 | A02 | 12479180 | C | T | synonymous_variant | LOW | c.915C>T|p.Pro305Pro |
S118 |
13 | BAA02g22950 | A02 | 12479872 | G | A | missense_variant | MODERATE | c.1189G>A|p.Glu397Lys |
S61 |
14 | BAA02g22950 | A02 | 12479887 | G | A | missense_variant | MODERATE | c.1204G>A|p.Gly402Arg |
S230 |