Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g18850 | A08 | 14966219 | C | T | upstream_gene_variant | MODIFIER | c.-1613C>T| |
S249 |
2 | BAA08g18850 | A08 | 14966230 | G | A | upstream_gene_variant | MODIFIER | c.-1602G>A| |
S203 |
3 | BAA08g18850 | A08 | 14966562 | C | T | upstream_gene_variant | MODIFIER | c.-1270C>T| |
S201 |
4 | BAA08g18850 | A08 | 14966807 | G | A | upstream_gene_variant | MODIFIER | c.-1025G>A| |
S302 |
5 | BAA08g18850 | A08 | 14966970 | G | A | upstream_gene_variant | MODIFIER | c.-862G>A| |
S119 |
6 | BAA08g18850 | A08 | 14967011 | G | A | upstream_gene_variant | MODIFIER | c.-821G>A| |
S306 |
7 | BAA08g18850 | A08 | 14968716 | C | T | synonymous_variant | LOW | c.519C>T|p.Thr173Thr |
S293 |
8 | BAA08g18850 | A08 | 14968761 | C | T | synonymous_variant | LOW | c.564C>T|p.Phe188Phe |
S39 |
9 | BAA08g18850 | A08 | 14969732 | G | A | stop_gained | HIGH | c.1161G>A|p.Trp387* |
S12 |