Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g25870 | A09 | 16727803 | C | T | upstream_gene_variant | MODIFIER | c.-4922C>T| |
S234 |
2 | BAA09g25870 | A09 | 16727948 | G | A | upstream_gene_variant | MODIFIER | c.-4777G>A| |
S184 |
3 | BAA09g25870 | A09 | 16728138 | C | T | upstream_gene_variant | MODIFIER | c.-4587C>T| |
S60 |
4 | BAA09g25870 | A09 | 16728706 | G | A | upstream_gene_variant | MODIFIER | c.-4019G>A| |
S162 |
5 | BAA09g25870 | A09 | 16730118 | C | T | upstream_gene_variant | MODIFIER | c.-2607C>T| |
S293 |
6 | BAA09g25870 | A09 | 16730167 | C | T | upstream_gene_variant | MODIFIER | c.-2558C>T| |
S63 |
7 | BAA09g25870 | A09 | 16730461 | G | A | upstream_gene_variant | MODIFIER | c.-2264G>A| |
S280 |
8 | BAA09g25870 | A09 | 16731262 | C | T | upstream_gene_variant | MODIFIER | c.-1463C>T| |
S32 |
9 | BAA09g25870 | A09 | 16733364 | C | T | missense_variant | MODERATE | c.640C>T|p.Pro214Ser |
S174 S27 |
10 | BAA09g25870 | A09 | 16737426 | A | C | downstream_gene_variant | MODIFIER | c.*3577A>C| |
S281 |