Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g65850 | A09 | 60456097 | G | A | missense_variant | MODERATE | c.997C>T|p.Leu333Phe |
S38 |
2 | BAA09g65850 | A09 | 60456306 | C | T | missense_variant | MODERATE | c.788G>A|p.Arg263Gln |
S95 |
3 | BAA09g65850 | A09 | 60456599 | C | T | synonymous_variant | LOW | c.573G>A|p.Gln191Gln |
S306 S308 |
4 | BAA09g65850 | A09 | 60457467 | G | A | synonymous_variant | LOW | c.240C>T|p.Thr80Thr |
S185 |
5 | BAA09g65850 | A09 | 60461052 | C | T | upstream_gene_variant | MODIFIER | c.-3261G>A| |
S192 |
6 | BAA09g65850 | A09 | 60462731 | C | T | upstream_gene_variant | MODIFIER | c.-4940G>A| |
S107 |