Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g07690 | A02 | 3297592 | G | A | missense_variant | MODERATE | c.22G>A|p.Ala8Thr |
S157 |
2 | BAA02g07690 | A02 | 3297996 | G | A | synonymous_variant | LOW | c.426G>A|p.Ser142Ser |
S264 |
3 | BAA02g07690 | A02 | 3298197 | C | T | synonymous_variant | LOW | c.627C>T|p.Leu209Leu |
S71 |
4 | BAA02g07690 | A02 | 3298666 | G | A | missense_variant | MODERATE | c.1096G>A|p.Gly366Arg |
S92 |
5 | BAA02g07690 | A02 | 3298691 | G | A | missense_variant | MODERATE | c.1121G>A|p.Gly374Glu |
S232 |
6 | BAA02g07690 | A02 | 3298867 | C | T | missense_variant | MODERATE | c.1297C>T|p.Pro433Ser |
S295 |
7 | BAA02g07690 | A02 | 3300798 | G | A | synonymous_variant | LOW | c.3228G>A|p.Arg1076Arg |
S136 |