Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g10760 | A01 | 4956245 | A | C | missense_variant | MODERATE | c.17A>C|p.Lys6Thr |
S184 |
2 | BAA01g10760 | A01 | 4956691 | G | A | missense_variant | MODERATE | c.463G>A|p.Val155Ile |
S247 |
3 | BAA01g10760 | A01 | 4956761 | C | T | missense_variant | MODERATE | c.533C>T|p.Ser178Phe |
S139 |
4 | BAA01g10760 | A01 | 4957590 | C | T | synonymous_variant | LOW | c.1176C>T|p.Asn392Asn |
S305 |
5 | BAA01g10760 | A01 | 4957612 | G | A | missense_variant | MODERATE | c.1198G>A|p.Gly400Arg |
S281 |
6 | BAA01g10760 | A01 | 4958403 | C | T | synonymous_variant | LOW | c.1662C>T|p.Ser554Ser |
S50 |
7 | BAA01g10760 | A01 | 4958408 | C | T | missense_variant | MODERATE | c.1667C>T|p.Thr556Ile |
S268 |
8 | BAA01g10760 | A01 | 4962947 | G | A | downstream_gene_variant | MODIFIER | c.*4445G>A| |
S119 |