Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g43430 | A01 | 28760237 | C | T | missense_variant | MODERATE | c.2128G>A|p.Val710Ile |
S282 |
2 | BAA01g43430 | A01 | 28760781 | G | A | missense_variant | MODERATE | c.1769C>T|p.Thr590Ile |
S302 |
3 | BAA01g43430 | A01 | 28761323 | C | T | synonymous_variant | LOW | c.1422G>A|p.Lys474Lys |
S279 |
4 | BAA01g43430 | A01 | 28762014 | C | T | missense_variant | MODERATE | c.973G>A|p.Gly325Arg |
S19 |
5 | BAA01g43430 | A01 | 28762561 | C | T | synonymous_variant | LOW | c.426G>A|p.Lys142Lys |
S161 |
6 | BAA01g43430 | A01 | 28762692 | C | T | missense_variant | MODERATE | c.295G>A|p.Asp99Asn |
S270 |
7 | BAA01g43430 | A01 | 28762972 | G | A | synonymous_variant | LOW | c.15C>T|p.His5His |
S139 |
8 | BAA01g43430 | A01 | 28767883 | A | G | upstream_gene_variant | MODIFIER | c.-4897T>C| |
S166 |