Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g15960 | A07 | 22968306 | C | T | missense_variant | MODERATE | c.488C>T|p.Thr163Ile |
S221 |
2 | BAA07g15960 | A07 | 22968350 | G | A | missense_variant | MODERATE | c.532G>A|p.Ala178Thr |
S183 |
3 | BAA07g15960 | A07 | 22968473 | G | A | missense_variant | MODERATE | c.655G>A|p.Glu219Lys |
S45 |