Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00020 | A10 | 7522 | C | T | upstream_gene_variant | MODIFIER | c.-3052C>T| |
S6 |
2 | BAA10g00020 | A10 | 8097 | C | T | upstream_gene_variant | MODIFIER | c.-2477C>T| |
S42 |
3 | BAA10g00020 | A10 | 8856 | G | A | upstream_gene_variant | MODIFIER | c.-1718G>A| |
S223 |
4 | BAA10g00020 | A10 | 8889 | G | A | upstream_gene_variant | MODIFIER | c.-1685G>A| |
S262 |
5 | BAA10g00020 | A10 | 9263 | G | A | upstream_gene_variant | MODIFIER | c.-1311G>A| |
S192 |
6 | BAA10g00020 | A10 | 9640 | G | A | upstream_gene_variant | MODIFIER | c.-934G>A| |
S94 |
7 | BAA10g00020 | A10 | 9820 | G | A | upstream_gene_variant | MODIFIER | c.-754G>A| |
S290 |
8 | BAA10g00020 | A10 | 9844 | G | A | upstream_gene_variant | MODIFIER | c.-730G>A| |
S212 |
9 | BAA10g00020 | A10 | 10231 | C | T | upstream_gene_variant | MODIFIER | c.-343C>T| |
S204 |
10 | BAA10g00020 | A10 | 10454 | G | A | upstream_gene_variant | MODIFIER | c.-120G>A| |
S217 |
11 | BAA10g00020 | A10 | 11783 | G | A | downstream_gene_variant | MODIFIER | c.*330G>A| |
S9 |