Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g26890 | A10 | 21135886 | C | T | upstream_gene_variant | MODIFIER | c.-4455C>T| |
S161 |
2 | BAA10g26890 | A10 | 21137458 | G | A | upstream_gene_variant | MODIFIER | c.-2883G>A| |
S250 |
3 | BAA10g26890 | A10 | 21138245 | C | T | upstream_gene_variant | MODIFIER | c.-2096C>T| |
S162 |
4 | BAA10g26890 | A10 | 21138598 | G | A | upstream_gene_variant | MODIFIER | c.-1743G>A| |
S212 |
5 | BAA10g26890 | A10 | 21139421 | G | A | upstream_gene_variant | MODIFIER | c.-920G>A| |
S257 |
6 | BAA10g26890 | A10 | 21139509 | C | T | upstream_gene_variant | MODIFIER | c.-832C>T| |
S283 |
7 | BAA10g26890 | A10 | 21139563 | G | A | upstream_gene_variant | MODIFIER | c.-778G>A| |
S208 S219 |
8 | BAA10g26890 | A10 | 21139574 | C | T | upstream_gene_variant | MODIFIER | c.-767C>T| |
S166 |
9 | BAA10g26890 | A10 | 21139636 | C | T | upstream_gene_variant | MODIFIER | c.-705C>T| |
S115 |
10 | BAA10g26890 | A10 | 21139691 | G | A | upstream_gene_variant | MODIFIER | c.-650G>A| |
S125 |
11 | BAA10g26890 | A10 | 21143303 | C | T | downstream_gene_variant | MODIFIER | c.*2645C>T| |
S38 |