Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g12630 | A02 | 5653168 | G | A | missense_variant | MODERATE | c.526G>A|p.Ala176Thr |
S269 |
2 | BAA02g12630 | A02 | 5653299 | G | A | synonymous_variant | LOW | c.657G>A|p.Lys219Lys |
S156 |
3 | BAA02g12630 | A02 | 5653368 | G | A | synonymous_variant | LOW | c.726G>A|p.Glu242Glu |
S67 |
4 | BAA02g12630 | A02 | 5653522 | G | A | missense_variant | MODERATE | c.880G>A|p.Gly294Ser |
S37 |
5 | BAA02g12630 | A02 | 5653828 | C | T | missense_variant | MODERATE | c.1102C>T|p.Pro368Ser |
S212 |
6 | BAA02g12630 | A02 | 5653874 | C | T | missense_variant | MODERATE | c.1148C>T|p.Ala383Val |
S216 |
7 | BAA02g12630 | A02 | 5654390 | C | T | synonymous_variant | LOW | c.1513C>T|p.Leu505Leu |
S115 |
8 | BAA02g12630 | A02 | 5654682 | C | T | missense_variant | MODERATE | c.1805C>T|p.Ser602Phe |
S219 S72 |
9 | BAA02g12630 | A02 | 5654694 | C | T | missense_variant | MODERATE | c.1817C>T|p.Ser606Phe |
S87 |
10 | BAA02g12630 | A02 | 5654756 | C | T | missense_variant | MODERATE | c.1879C>T|p.Leu627Phe |
S159 S188 S243 S276 S298 S299 |
11 | BAA02g12630 | A02 | 5655027 | C | T | synonymous_variant | LOW | c.2070C>T|p.Asn690Asn |
S78 S83 |