Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g22890 | A01 | 11628772 | G | A | missense_variant | MODERATE | c.889C>T|p.His297Tyr |
S294 |
2 | BAA01g22890 | A01 | 11628939 | G | A | missense_variant | MODERATE | c.722C>T|p.Ser241Phe |
S94 |
3 | BAA01g22890 | A01 | 11629369 | C | T | missense_variant | MODERATE | c.292G>A|p.Glu98Lys |
S130 |
4 | BAA01g22890 | A01 | 11629449 | G | A | missense_variant | MODERATE | c.212C>T|p.Ser71Phe |
S234 |
5 | BAA01g22890 | A01 | 11629471 | C | T | missense_variant | MODERATE | c.190G>A|p.Glu64Lys |
S11 |
6 | BAA01g22890 | A01 | 11629585 | G | A | missense_variant | MODERATE | c.76C>T|p.Leu26Phe |
S275 |
7 | BAA01g22890 | A01 | 11629657 | C | T | missense_variant | MODERATE | c.4G>A|p.Asp2Asn |
S179 |
8 | BAA01g22890 | A01 | 11629744 | C | T | upstream_gene_variant | MODIFIER | c.-84G>A| |
S291 |
9 | BAA01g22890 | A01 | 11631873 | G | A | upstream_gene_variant | MODIFIER | c.-2213C>T| |
S229 |
10 | BAA01g22890 | A01 | 11632960 | G | A | upstream_gene_variant | MODIFIER | c.-3300C>T| |
S71 |