Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00120 | A10 | 46743 | C | T | missense_variant | MODERATE | c.833G>A|p.Arg278Gln |
S142 |
2 | BAA10g00120 | A10 | 47465 | G | A | synonymous_variant | LOW | c.111C>T|p.Ala37Ala |
S125 |
3 | BAA10g00120 | A10 | 47538 | G | A | missense_variant | MODERATE | c.38C>T|p.Thr13Ile |
S176 |