Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g64660 | A09 | 59904635 | G | A | missense_variant | MODERATE | c.2408C>T|p.Ala803Val |
S107 |
2 | BAA09g64660 | A09 | 59905543 | C | T | missense_variant | MODERATE | c.1742G>A|p.Gly581Glu |
S280 |
3 | BAA09g64660 | A09 | 59906021 | C | T | splice_donor_variant&intron_variant | HIGH | c.1414+1G>A| |
S171 |
4 | BAA09g64660 | A09 | 59907189 | G | A | missense_variant | MODERATE | c.319C>T|p.Leu107Phe |
S110 |
5 | BAA09g64660 | A09 | 59912054 | C | T | upstream_gene_variant | MODIFIER | c.-4547G>A| |
S156 S34 S4 S6 |