Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g06660 | A02 | 2837468 | G | A | upstream_gene_variant | MODIFIER | c.-3634G>A| |
S10 |
2 | BAA02g06660 | A02 | 2837615 | G | A | upstream_gene_variant | MODIFIER | c.-3487G>A| |
S91 |
3 | BAA02g06660 | A02 | 2841291 | C | T | synonymous_variant | LOW | c.190C>T|p.Leu64Leu |
S120 |
4 | BAA02g06660 | A02 | 2841749 | G | A | synonymous_variant | LOW | c.648G>A|p.Gln216Gln |
S187 S243 S298 |
5 | BAA02g06660 | A02 | 2841802 | G | A | missense_variant | MODERATE | c.701G>A|p.Gly234Glu |
S303 |
6 | BAA02g06660 | A02 | 2841906 | G | A | missense_variant | MODERATE | c.805G>A|p.Asp269Asn |
S264 |
7 | BAA02g06660 | A02 | 2842017 | C | T | missense_variant | MODERATE | c.916C>T|p.Pro306Ser |
S216 |
8 | BAA02g06660 | A02 | 2845131 | C | T | downstream_gene_variant | MODIFIER | c.*2836C>T| |
S180 |
9 | BAA02g06660 | A02 | 2845746 | G | A | downstream_gene_variant | MODIFIER | c.*3451G>A| |
S52 |
10 | BAA02g06660 | A02 | 2846544 | C | T | downstream_gene_variant | MODIFIER | c.*4249C>T| |
S76 |
11 | BAA02g06660 | A02 | 2846672 | C | T | downstream_gene_variant | MODIFIER | c.*4377C>T| |
S120 |
12 | BAA02g06660 | A02 | 2847251 | C | T | downstream_gene_variant | MODIFIER | c.*4956C>T| |
S40 S49 S55 |