Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g23880 | A09 | 15215847 | G | A | missense_variant | MODERATE | c.886G>A|p.Glu296Lys |
S4 |
2 | BAA09g23880 | A09 | 15215965 | C | T | missense_variant | MODERATE | c.1004C>T|p.Ser335Phe |
S153 |
3 | BAA09g23880 | A09 | 15216268 | G | A | missense_variant | MODERATE | c.1307G>A|p.Gly436Glu |
S184 |
4 | BAA09g23880 | A09 | 15217188 | G | A | missense_variant | MODERATE | c.1978G>A|p.Ala660Thr |
S259 |
5 | BAA09g23880 | A09 | 15217565 | C | T | missense_variant | MODERATE | c.2246C>T|p.Ala749Val |
S221 |
6 | BAA09g23880 | A09 | 15218244 | G | T | missense_variant | MODERATE | c.2486G>T|p.Gly829Val |
S213 |
7 | BAA09g23880 | A09 | 15218852 | G | A | synonymous_variant | LOW | c.2808G>A|p.Lys936Lys |
S86 |
8 | BAA09g23880 | A09 | 15219712 | G | A | missense_variant | MODERATE | c.3299G>A|p.Gly1100Asp |
S276 |