Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g44600 | A09 | 50190080 | G | A | missense_variant | MODERATE | c.463C>T|p.Leu155Phe |
S70 |
2 | BAA09g44600 | A09 | 50190533 | C | T | splice_region_variant&intron_variant | LOW | c.179+5G>A| |
S153 |
3 | BAA09g44600 | A09 | 50194064 | A | C | upstream_gene_variant | MODIFIER | c.-3279T>G| |
S156 S168 S185 S193 S200 S211 S246 S282 S38 |
4 | BAA09g44600 | A09 | 50194963 | G | A | upstream_gene_variant | MODIFIER | c.-4178C>T| |
S176 |