Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g06030 | A10 | 3103303 | G | A | upstream_gene_variant | MODIFIER | c.-4952G>A| |
S78 S83 |
2 | BAA10g06030 | A10 | 3103450 | G | A | upstream_gene_variant | MODIFIER | c.-4805G>A| |
S186 |
3 | BAA10g06030 | A10 | 3103708 | C | T | upstream_gene_variant | MODIFIER | c.-4547C>T| |
S287 |
4 | BAA10g06030 | A10 | 3103874 | C | T | upstream_gene_variant | MODIFIER | c.-4381C>T| |
S308 |
5 | BAA10g06030 | A10 | 3104401 | G | A | upstream_gene_variant | MODIFIER | c.-3854G>A| |
S208 S219 |
6 | BAA10g06030 | A10 | 3104417 | G | A | upstream_gene_variant | MODIFIER | c.-3838G>A| |
S57 |
7 | BAA10g06030 | A10 | 3104534 | C | T | upstream_gene_variant | MODIFIER | c.-3721C>T| |
S155 S211 |
8 | BAA10g06030 | A10 | 3104799 | C | T | upstream_gene_variant | MODIFIER | c.-3456C>T| |
S166 |
9 | BAA10g06030 | A10 | 3108674 | G | A | missense_variant | MODERATE | c.356G>A|p.Gly119Asp |
S208 S219 |
10 | BAA10g06030 | A10 | 3110965 | G | A | downstream_gene_variant | MODIFIER | c.*1475G>A| |
S125 |