Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g38170 | A03 | 17653469 | G | A | missense_variant | MODERATE | c.1534C>T|p.Pro512Ser |
S15 S156 S2 S3 S34 |
2 | BAA03g38170 | A03 | 17653639 | G | A | missense_variant | MODERATE | c.1364C>T|p.Thr455Ile |
S223 |
3 | BAA03g38170 | A03 | 17653886 | C | T | missense_variant | MODERATE | c.1192G>A|p.Glu398Lys |
S159 S243 |
4 | BAA03g38170 | A03 | 17653997 | C | T | missense_variant | MODERATE | c.1081G>A|p.Ala361Thr |
S125 |
5 | BAA03g38170 | A03 | 17654667 | G | A | synonymous_variant | LOW | c.642C>T|p.Leu214Leu |
S289 S290 |
6 | BAA03g38170 | A03 | 17654684 | G | A | missense_variant | MODERATE | c.625C>T|p.Leu209Phe |
S246 |
7 | BAA03g38170 | A03 | 17655167 | C | T | missense_variant | MODERATE | c.142G>A|p.Gly48Arg |
S100 |
8 | BAA03g38170 | A03 | 17660264 | C | T | upstream_gene_variant | MODIFIER | c.-4956G>A| |
S187 |