Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g38170 | A06 | 25053908 | G | A | missense_variant | MODERATE | c.1412C>T|p.Ser471Leu |
S249 |
2 | BAA06g38170 | A06 | 25053944 | G | A | missense_variant | MODERATE | c.1376C>T|p.Thr459Ile |
S210 S225 |
3 | BAA06g38170 | A06 | 25054566 | C | T | missense_variant | MODERATE | c.754G>A|p.Ala252Thr |
S247 |
4 | BAA06g38170 | A06 | 25055391 | G | A | missense_variant | MODERATE | c.196C>T|p.Pro66Ser |
S210 |
5 | BAA06g38170 | A06 | 25055578 | C | T | synonymous_variant | LOW | c.9G>A|p.Arg3Arg |
S150 |
6 | BAA06g38170 | A06 | 25055583 | C | T | missense_variant | MODERATE | c.4G>A|p.Ala2Thr |
S291 |
7 | BAA06g38170 | A06 | 25060462 | C | T | upstream_gene_variant | MODIFIER | c.-4876G>A| |
S165 |