Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g11480 | A08 | 10183713 | G | A | upstream_gene_variant | MODIFIER | c.-1804G>A| |
S87 |
2 | BAA08g11480 | A08 | 10184104 | C | G | upstream_gene_variant | MODIFIER | c.-1413C>G| |
S35 |
3 | BAA08g11480 | A08 | 10184362 | C | T | upstream_gene_variant | MODIFIER | c.-1155C>T| |
S208 S219 |
4 | BAA08g11480 | A08 | 10184650 | C | T | upstream_gene_variant | MODIFIER | c.-867C>T| |
S302 |
5 | BAA08g11480 | A08 | 10184765 | G | A | upstream_gene_variant | MODIFIER | c.-752G>A| |
S128 |
6 | BAA08g11480 | A08 | 10184925 | G | A | upstream_gene_variant | MODIFIER | c.-592G>A| |
S131 |
7 | BAA08g11480 | A08 | 10184979 | C | T | upstream_gene_variant | MODIFIER | c.-538C>T| |
S79 S84 |
8 | BAA08g11480 | A08 | 10185352 | C | T | upstream_gene_variant | MODIFIER | c.-165C>T| |
S268 |
9 | BAA08g11480 | A08 | 10186140 | C | T | missense_variant | MODERATE | c.296C>T|p.Ser99Leu |
S156 |