Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g45740 | A09 | 50817138 | C | T | missense_variant | MODERATE | c.169C>T|p.Leu57Phe |
S117 |
2 | BAA09g45740 | A09 | 50817331 | C | T | synonymous_variant | LOW | c.270C>T|p.Tyr90Tyr |
S251 |
3 | BAA09g45740 | A09 | 50817507 | G | A | splice_region_variant&stop_retained_variant | LOW | c.357G>A|p.Ter119Ter |
S262 |
4 | BAA09g45740 | A09 | 50822297 | C | T | downstream_gene_variant | MODIFIER | c.*4790C>T| |
S37 |