Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g45270 | A09 | 50518668 | G | A | missense_variant | MODERATE | c.328C>T|p.Leu110Phe |
S45 |
2 | BAA09g45270 | A09 | 50518908 | C | T | splice_region_variant&intron_variant | LOW | c.178-4G>A| |
S155 |
3 | BAA09g45270 | A09 | 50522031 | C | T | upstream_gene_variant | MODIFIER | c.-2309G>A| |
S293 |
4 | BAA09g45270 | A09 | 50522043 | G | A | upstream_gene_variant | MODIFIER | c.-2321C>T| |
S166 |
5 | BAA09g45270 | A09 | 50523338 | C | T | upstream_gene_variant | MODIFIER | c.-3616G>A| |
S59 |